iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

Atg10

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6233379	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90975241	CCTCATCGGTTACTA[C/T]GTAGTAATGTAGTAT	66795
rs6235066	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90975583	tattttctttattta[C/T]atttcaaatgttatc	66795
rs6235598	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90975676	acccacccttgcctc[C/T]ccatcctggcattcc	66795
rs6257910	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91028608	gtttttgctatcctc[A/G]gtttttCCCTATCTC	66795
rs6258402	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91094734	GTGTACATTTGGCTC[C/T]GTTTCCGTAACTGTT	66795
rs6258859	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91094816	CTTTTAACCCTTCTG[C/T]GTATGGGGAAAACTG	66795
rs6258901	snp	A/C	0.5	0	intron-variant	Atg10	Mm_Celera	13:91094844	CTGGTTTTCTTTAAG[A/C]GCTTTTGAGTGAACA	66795
rs6272767	snp	C/T	0.21875	0.248039	intron-variant	Atg10	Mm_Celera	13:91135311	ATCATTTGCACTTAT[C/T]GTCATATCTATACTT	66795
rs6273924	snp	A/C	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:91135504	GGGCAGTGGGCATAT[A/C]GGAAGACAGGCTTCT	66795
rs6274417	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956800	aatgctgaacttctg[C/T]agcataaaatgctct	66795
rs6274497	snp	A/G	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:91135607	CTTCAGGGAGTTTAC[A/G]ATGGGTTGTTTTCGT	66795
rs6274536	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956859	gtatcattcttcttc[A/G]aatcatggaccctga	66795
rs6275013	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956919	ttttgaactcatgct[C/T]ttagagttctttccc	66795
rs6275085	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956965	gtcctgaaggtcaca[A/G]cnttctaccattttg	66795
rs6275086	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90956967	cctgaaggtcacanc[A/G]ttctaccattttgct	66795
rs6276675	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90957249	gcaggaaccatgtca[C/T]gctgtcccttccatg	66795
rs6288319	snp	C/T	0.456747	0.140554	intron-variant	Atg10	GRCm38.p3	13:91135890	CCTCTGCAAAAGAAA[C/T]GGAATGTCAGTAATG	66795
rs6288428	snp	A/G	0.359862	0.224567	intron-variant	Atg10	Mm_Celera	13:91135969	GTAATTCCCTTGCAA[A/G]TGTTCGCTGGTAATT	66795
rs6310977	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90997902	aaacttgtatagcca[C/T]gatggaaatcaatat	66795
rs6311488	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90997999	ACCAAAGGACCCTCC[A/C]TCTTACCACAAGGAC	66795
rs29221652	snp	G/T	0.459184	0.136902	intron-variant	Atg10	GRCm38.p3	13:91005214	GTTGAAAGATGAGAA[G/T]TACTTCAATTCTAAT	66795
rs29223118	snp	C/G	0.265928	0.249492	intron-variant	Atg10, Gm35245	Mm_Celera	13:90964373	TGTTACTAAATCACA[C/G]TGTATACCACAATGA	66795
rs29223712	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91151894	GTGATAAGAAGGAAG[A/G]GATAAGGGTTCCACT	66795
rs29223880	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90946542	GTAAAAATCATATGG[C/T]ATTGACATTAAAACA	66795
rs29223928	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90947539	GGAGACAGGAATGGG[C/T]GGGATCTGGTGGAGG	66795
rs29224249	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90981652	GGAAAGTGAAGGCTA[C/T]AGGAGAAACAGATCC	66795
rs29224276	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91040670	TGGGATGATATCATT[A/C]ACTATGAAGTCTGCT	66795
rs29224525	snp	C/G/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91158149	GAAGCCCAAGGTCAG[C/G/T]CCGCTCAACTGAGAT	66795
rs29224904	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91063802	TTTCCTCTTTCTCCA[C/T]ATCCTCTCCAGCATT	66795
rs29225051	snp	C/T	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:91095025	GCACAGAGTAGATGG[C/T]AGACGCAGGTCAGAG	66795
rs29225083	snp	C/G	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91139177	TGTCAGACTCTGACA[C/G]TAGTCAGCCTCCGAA	66795
rs29225142	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91216163	GCTGAAGTGTCACTT[A/G]AGTCTGTGAGCTTAA	66795
rs29225399	snp	C/T	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:90976489	TCCAGTTTTATAGAG[C/T]TGTTTTTCAATTGTT	66795
rs29225573	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Atg10	GRCm38.p3	13:91166320	CACTATATCTTAAAA[A/G]CAGTCCCTGAAAGAA	66795
rs29225585	snp	A/T	0.492188	0.0620098	intron-variant	Atg10	GRCm38.p3	13:91082048	TAGAGAAACTGTTGA[A/T]GGGTGTCTATTTGGC	66795
rs29225657	snp	A/G	0.391111	0.206368	intron-variant	Atg10	Mm_Celera	13:90957418	TCAGTAGGTCCTGTA[A/G]AACTGAAAGACACAA	66795
rs29225975	snp	A/G	0.32	0.24	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90970428	GTAGAAATTTCGGAG[A/G]ATCTCTCTCTGCCTA	66795
rs29226115	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90988447	AACGCTACGTGGACA[A/G]TACTTCATACCAAAC	66795
rs29226151	snp	A/C	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:91112501	TTGAATTTATATGTT[A/C]ATTTTACTGACTTCT	66795
rs29226156	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Atg10	Mm_Celera	13:90937002	GCTGCCTATATTCAA[A/G]TCCCAGTCCCACCCC	66795
rs29227050	snp	A/T	0.277778	0.248452	intron-variant	Atg10, Gm35245	Mm_Celera	13:90963682	CGCGTAAGTCAAAGG[A/T]CACAGTTTCTTCTCC	66795
rs29227270	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91076829	TTCCCACAAGCTCAC[A/G]TTTGCTTAATACATG	66795
rs29227384	snp	A/G	0.48	0.0979796	intron-variant	Atg10	Mm_Celera	13:90947017	TGTGGATCAAGGGGA[A/G]CACTCCTCCATAAAC	66795
rs29227835	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91180209	CAGCTACAAGGATAA[C/T]AGGCAACTACTGAGT	66795
rs29228090	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90942523	GAATAAAAAGACACT[A/G]ACTACAATATGTACT	66795
rs29228170	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91058706	CAGGCAAATGGATGG[A/G]ACTAGAAAATATCAT	66795
rs29228232	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91119307	TGTTCACAAAGGCAA[C/T]ACAGGTCTGGGGTTC	66795
rs29228426	snp	G/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91126647	ACTTCTACCTTGACT[G/T]AGCAGCACAGTGGAG	66795
rs29228656	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91080301	TTAACAGTGGTTCAA[A/G]CAATATGAACTAACC	66795
rs29228722	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91198885	CATAACACACACACA[C/T]ATATATATATGAAAT	66795
rs29228833	snp	A/G	0.42	0.183303	intron-variant	Atg10	GRCm38.p3	13:91036575	TTGGGTGCATTTTAC[A/G]TTCTATATCCTGGCT	66795
rs29228900	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91075970	AATTCTGACACTGAT[A/G]TGTATGTGTCCTGGA	66795
rs29229243	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91017273	AGCATGACACTACCC[A/G]GTCAAAATTCTACCA	66795
rs29229362	snp	C/T	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91034934	ACACATATACACACA[C/T]ACACACAGATGTGTG	66795
rs29229411	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90982808	CAAGGCCCTGGAAGC[A/G]CAAAGGGTTTTGGGG	66795
rs29229439	snp	A/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91169760	AGCAAGTTTGCAAGG[A/T]TGCATGGGGAGAGTT	66795
rs29229742	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91063273	GAGAGGGGTTGAAAG[C/T]GTTGAACATTTCCTG	66795
rs29230000	snp	C/T	0.387812	0.208586	intron-variant	Atg10	GRCm38.p3	13:91049176	CTTAATTTTATTGTG[C/T]CTTTATAAGCAGAAA	66795
rs29230101	snp	A/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90947272	GCATAATGAAGTATT[A/T]CTCAGCTGTGAAAAA	66795
rs29230296	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91114320	AGGAACTGCTCTGAC[C/T]CTTCCTAGCCAAGGT	66795
rs29231074	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91042289	TTATGGGATGTGGAA[C/T]AGTCGGCAGGTGGAC	66795
rs29231153	snp	A/G	0.493827	0.0552116	intron-variant	Atg10	GRCm38.p3	13:91112478	CACATAAAAATACTC[A/G]TCCTAGTTTGAATTT	66795
rs29231456	snp	A/C	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91156008	CTTGGAAGCTTGCTA[A/C]TTATGACTCAATTCT	66795
rs29231458	snp	A/T	0.277778	0.248452	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90971296	ACAATAGAGTTAATT[A/T]TAAATTTGGCAAATT	66795
rs29231487	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91185798	ACAAGCAAAACACCA[C/T]CCAACACAACTGACT	66795
rs29231694	snp	C/T	0.387812	0.208586	intron-variant	Atg10	GRCm38.p3	13:91048040	GCAAGAGAGCCCATA[C/T]AGCCTCTTTAAAAGG	66795
rs29231947	snp	C/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Atg10	Mm_Celera	13:90936863	GTGATCCGAGGTTTT[C/G]TGAAGATCTCTCACC	66795
rs29232019	snp	A/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91159412	AAGCATTTATTAGAT[A/T]TATATGCTATGTGTG	66795
rs29233172	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91099556	TGCCATTCCCTCACA[C/T]CACCCATCTTCCTGC	66795
rs29233258	snp	A/C	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:90981468	TGGTCATCACACTGA[A/C]GAAAGCCTCAATGCT	66795
rs29233368	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91123028	AGAGTCCAAGAGAGC[C/T]CAGAAAACAATGCAG	66795
rs29233674	snp	A/G	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91156097	TTAATATCATTCCTG[A/G]CTGGAGAGTAAACTA	66795
rs29233868	snp	A/C	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91113413	ATGCATAAGACATGA[A/C]CAGGTAAAGTCACAC	66795
rs29233891	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91122866	ATATATATATATATA[C/T]ATACATATATATATA	66795
rs29234038	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91206761	AGGGAAATACTTGAG[C/T]ATATCAGGCTTTTTT	66795
rs29234441	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91181059	ATGGGCTTCATTCTA[C/T]GTGTTTAATGCCAGC	66795
rs29234960	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91219573	GAGTTGGGGGTGTGT[C/T]CAGGAATAAAAGGGC	66795
rs29235103	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91179708	ACCAGGAAGAAGCAC[A/G]TGTGCCAAGCTGCCA	66795
rs29235466	snp	C/T	0.429688	0.173817	intron-variant	Atg10	Mm_Celera	13:91193314	TGCTTCCTCGGAGTG[C/T]ATGCACAGCTGCCAG	66795
rs29235936	snp	G/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91120403	AATTTTATTTGTAAT[G/T]CATTTTTTACACTCC	66795
rs29236062	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90948688	TGACTCTGATTATGG[A/G]GTATAGCGGTTAAGG	66795
rs29236321	snp	A/G	0.497778	0.0332592	intron-variant	Atg10	GRCm38.p3	13:91157747	AATACCATAAATAAA[A/G]ATCCAAATTACTTCT	66795
rs29236478	snp	A/T	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Atg10	Mm_Celera	13:91224202	CCAGGGTATCTGCAC[A/T]CCCTTCCCCACACGC	66795
rs29236575	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91067082	CATAGAAAAAGATAA[A/G]GAAGGACACTTCATA	66795
rs29236811	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90949921	CAGACCAAGTAGGTG[C/T]CTTAGTTAAGGTTAT	66795
rs29237019	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91179717	AAGCACATGTGCCAA[A/G]CTGCCACACTCGGAA	66795
rs29237125	snp	G/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91071985	GAAGCCCTAGACAAC[G/T]TAGCAAATTACAATA	66795
rs29237126	snp	A/C	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91000313	AAGGGCTGCCTTGAT[A/C]ATGGTATCTGTTTAC	66795
rs29237303	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91192357	TCCCAGTGTAATCAA[A/G]TTACTATGTTGTGGA	66795
rs29237570	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90972715	CAATGGCTGCCCCCC[A/C]AAATATTCTCAAAAG	66795
rs29237584	snp	C/T	0.465374	0.126941	intron-variant	Atg10	GRCm38.p3	13:91077831	GCCATTATCTCTTCT[C/T]CCTTTCATACTGACT	66795
rs29237789	snp	C/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91184584	GGGTCAGCAAGCTGA[C/G]CTGTTCTCATGATAC	66795
rs29238088	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91059911	GCTGGCCCTGGTAGT[A/G]TGAGCACAGGAGAGA	66795
rs29238337	snp	A/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91155913	AATTTAAAGTTTTTT[A/T]AAAAATTAGAGAAAG	66795
rs29238578	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90947235	TCAACAGAAGAATGA[A/G]TAAATACACATTGGT	66795
rs29238833	snp	A/C	0.401235	0.199068	intron-variant	Atg10, Gm35245	Mm_Celera	13:90966163	TAAATGAAGCTGCCA[A/C]GTTACTCTGTTCAGT	66795
rs29239293	snp	C/T	0.492188	0.0620098	intron-variant	Atg10	GRCm38.p3	13:91116392	CCATGATGGTAACAT[C/T]AGAAACAAAGACCTC	66795
rs29239393	snp	C/T	0.336735	0.234472	intron-variant	Atg10, Gm35245	Mm_Celera	13:90967206	ATAATAATTAAAAGA[C/T]TTAATGCTCAGGTTG	66795
rs29239454	snp	C/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91009944	GTTCTGAAGAAGCAG[C/T]GGCAACCTATAAAGC	66795
rs29239943	snp	G/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91201095	GATAGAAATAAAAGA[G/T]TAGCTTTGAAGACAT	66795
rs29240012	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91070573	AATGTGGTACATTTA[C/T]ACAACGGAATATGAC	66795
rs29240241	snp	A/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91022261	GCTGATACTGGGCAT[A/T]CAATGAAGAGGAAAG	66795
rs29240418	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91212322	TTTCTGAGTTCGAGG[C/T]CAGCCCGGTCTACAG	66795
rs29240535	snp	A/C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91030241	GTGAATTGTTTTAGA[A/C/T]GTTTTCCATGTCATA	66795
rs29240724	snp	C/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91154020	ATCACAGTATATACA[C/G]CACAATTGCTGTTTT	66795
rs29240775	snp	C/G	0.5	0	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90971759	CATGATGTTGTGGAG[C/G]AACAGCATGGTGTAT	66795
rs29241839	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91000090	AGGTGTGGTCTTGTT[A/G]GAGTAGGTGTGTCAC	66795
rs29241875	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:90940322	TTAATAAAAATATGA[C/T]AAAAAGAGGAAAGAA	66795
rs29242001	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91119164	GCCGCCATGTAGGTG[C/T]TGGGGAGGAAACTCG	66795
rs29242527	snp	A/G	0.475309	0.108333	intron-variant	Atg10	GRCm38.p3	13:91079700	TCTCTAATGTAAGCC[A/G]TATTTGTTGGCATCT	66795
rs29242602	snp	C/T	0.429688	0.173817	intron-variant	Atg10	GRCm38.p3	13:91039377	CGTGAGCTCATCAGC[C/T]GGTCTCGGCAAGACC	66795
rs29243665	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91172507	CATTTCTTTTGTTTG[C/T]TTGTTTTTTCGAGAC	66795
rs29244675	snp	A/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91157038	CAACTAAGTAAGGGA[A/T]GACATAGGCTAGTGT	66795
rs29244723	snp	A/T	0.265928	0.249492	intron-variant	Atg10	Mm_Celera	13:91043135	TTGTTAAAGGTTTGG[A/T]TGTCATATATGATAC	66795
rs29244833	snp	C/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90947248	GAATAAATACACATT[C/G]GTACATCTGCATAAT	66795
rs29245173	snp	A/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90987250	TAATGTTAAGAAAGA[A/T]AATTTCAGAGACAGT	66795
rs29245483	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90988954	TTTAGTTGTTGAGCC[C/T]AGAGATTGAGTTACC	66795
rs29245613	snp	C/T	0.432133	0.171253	intron-variant	Atg10	Mm_Celera	13:90981251	CAATGACAGATAATG[C/T]CAGTTCCAGAATTGG	66795
rs29245863	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91113334	GTGGATACTTCCAAG[A/G]AAACAGTCTCTTTCA	66795
rs29246065	snp	C/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91025188	CAGTTCAGTGTTCTT[C/G]TTAAACCATGCTTCC	66795
rs29246295	snp	A/G	0.475309	0.108333	intron-variant	Atg10	Mm_Celera	13:91188515	AAGATTTGCAAATGC[A/G]GTTTACCTCCTTTTG	66795
rs29246360	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91064206	GGGGATCCATTCCAT[A/G]CAGACACCAAACCAA	66795
rs29246362	snp	G/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90947738	ATCTCCTGAAGCCAG[G/T]ACAGACTTCAGTGGT	66795
rs29246388	snp	C/G	0.432133	0.171253	intron-variant	Atg10	GRCm38.p3	13:91107413	GGTGAGGCCACAGGA[C/G]GAGAAGGCAACAAGG	66795
rs29246525	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91060310	CAGATATGGAGGGAT[C/T]CGGAGATGAGAGGGA	66795
rs29246740	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90947592	GAGTATGGGGAGAGA[A/C]TGCTGAAATTGGGGG	66795
rs29246857	snp	C/G	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91152520	AAGTCACATCAGAGT[C/G]GGCCTCTCATACTCT	66795
rs29247181	snp	A/C	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91058815	GGGGTGGTAAATACC[A/C]AAGATTCAGTCCACA	66795
rs29247570	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90948526	AAGCTTGGCAGTTTT[A/G]TGAAGGTAGTAGATA	66795
rs29247623	snp	A/G	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91041394	GTATGATTTTTAGCA[A/G]CAAGAGTTGTGAAAG	66795
rs29247707	snp	A/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91121990	TTTTCTAAAAAAAAA[A/T]TTTTTTTAAATAAGG	66795
rs29248166	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Atg10	Mm_Celera	13:91166918	GCTATCAGGAAGCCC[C/T]TCAGTGGCTCCTCAA	66795
rs29248503	snp	A/T	0.455	0.143091	intron-variant	Atg10	Mm_Celera	13:91177829	AGATTGTTGCAATAA[A/T]AAATACATGGGCTGA	66795
rs29249235	snp	G/T	0.486111	0.0821678	intron-variant	Atg10	GRCm38.p3	13:91113763	ATTTAATTTAAAAAG[G/T]TAACTGGTTGAGGAA	66795
rs29249361	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91178914	GGGCTCGCCATTCCA[C/T]GTATGGCTCTGCCTC	66795
rs29249532	snp	A/C	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91071441	TATCTAATAAAATAC[A/C]TATTAATTTAATAAT	66795
rs29250417	snp	A/G	0.489796	0.070696	intron-variant	Atg10	GRCm38.p3	13:91108028	TCCTAACCACACCTT[A/G]TTCCTTTTGTTCTTC	66795
rs29250817	snp	C/T	0.375	0.216506	intron-variant, utr-variant-5-prime	Atg10	Mm_Celera	13:91166139	ACTAGAGCCTGGGAA[C/T]CACAGGCAGATGAAG	66795
rs29251299	snp	A/C	0.493827	0.0552116	intron-variant	Atg10	GRCm38.p3	13:91045492	ATGCTACTTACAAGA[A/C]CCCAACGTGTAGAAT	66795
rs29251435	snp	G/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90949158	GGCATCAGCTCTCTT[G/T]GCACCAGAGCCTAGG	66795
rs29251557	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91003526	TTGTAGATGAGAAAC[C/T]TAAAGCATGAGGAAA	66795
rs29251732	snp	A/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91200953	TAAATAAATCTTTTT[A/T]AAAAAATAATGTACT	66795
rs29252061	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91223321	GGCAAGAGGCTCAAG[A/G]TAGGTAAAACAGGCA	66795
rs29252400	snp	C/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91025194	AGTGTTCTTGTTAAA[C/G]CATGCTTCCTCTGAC	66795
rs29252864	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91171723	TAGACCCTCCTGAAA[A/G]AAATCAACACAACCA	66795
rs29252865	snp	A/C	0.304688	0.243945	intron-variant	Atg10	GRCm38.p3	13:91199243	ATACAAAATCAAGTG[A/C]AACTGACTAGGATTC	66795
rs29252873	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90986150	CAGTCAGCATGGACA[C/T]CAGCTCCTGCCCAGG	66795
rs29493239	snp	A/C	0.444444	0.157135	upstream-variant-2KB	Atg10	Mm_Celera	13:91224933	TGTCAAAACAAAAAC[A/C]AAAAAAAGTGACATT	66795
rs29493632	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90951003	ACTGAACTGAGCAAC[C/T]GGGCACAGAGCAAAC	66795
rs29493650	snp	A/G	0.465374	0.126941	intron-variant	Atg10	Mm_Celera	13:91186232	ACTGGCTACCTAGGA[A/G]CTCTCATTTCATTTA	66795
rs29493741	snp	A/C	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91169199	AGCTACCGTCTAAGC[A/C]CACCCAGCTGCAGGC	66795
rs29493830	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91009698	GTCCTCAGCTCCGGG[A/G]AAAAAAAAAAAAAAG	66795
rs29493836	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91127144	TTTATGTTGCTGTTC[A/G]TTTGTTTGCGTGTGT	66795
rs29494837	snp	C/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91055565	TACCTTCTCCAAAAT[C/G]GACCATATAATTGGT	66795
rs29494926	snp	A/C	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91100700	CCACTCCATTTGCAT[A/C]GATATTGATTGCAGT	66795
rs29495027	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91076181	CATTATACCTCCTCC[C/T]CTTGAGGATCAGGGA	66795
rs29495092	snp	A/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91095901	AAGGAAGTGACTTCT[A/T]TATCCCCTTCAGACG	66795
rs29495501	snp	A/G	0.345679	0.230967	intron-variant	Atg10	Mm_Celera	13:90981632	TTCTCAGTTTGAGAT[A/G]AGGAGGAAAGTGAAG	66795
rs29495610	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91157857	TGTCTTCTAAAATAC[A/G]ATGAAAGAGCCAGGC	66795
rs29495901	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91022280	TGAAGAGGAAAGGGG[A/C]AAACCAGACATGATC	66795
rs29496075	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91191960	TGAGTCGAGTAGCAC[C/T]TGTAGTTGGGCATGC	66795
rs29496337	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91090702	ACACACACACACACA[C/T]ATATATATATATATA	66795
rs29496518	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91192930	TATATGGTATATATA[C/T]CATATATATATTCCA	66795
rs29496719	snp	A/T	0.456747	0.140554	intron-variant	Atg10	GRCm38.p3	13:91179049	ATAGCACAGCCTTTA[A/T]TGAAAACTTAACCCT	66795
rs29497004	snp	C/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91083889	TGTTCAAAATGTGAC[C/T]TTATTTTCACTAAAC	66795
rs29507712	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91040437	TAACCTAACCAATAA[A/G]CATTTCTTGAAATAA	66795
rs29508981	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91123707	CCAACACAATGACAA[C/T]GTGGACACTCTAATA	66795
rs29509362	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91040386	GAGGTGTGTAGATGA[C/T]TAGTGGAGGTGTTAC	66795
rs29510012	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91008259	CACCTTTCCTAGCAA[A/G]CCAGCTTCTAGACAG	66795
rs29510667	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90997855	TGGAAATGTGAAACA[A/G]GAGAAAATGCCCCCA	66795
rs29510858	snp	C/T	0.375	0.216506	intron-variant	Atg10, Gm35245	Mm_Celera	13:90965140	AAAGGAGCTTGCCAC[C/T]AGGTGTGACCAGCTG	66795
rs29511049	snp	C/T	0.290657	0.246672	intron-variant	Atg10, Gm35245	Mm_Celera	13:90963553	CACCCACAGCTGAAG[C/T]GTGACAGGGTCAGAG	66795
rs29511416	snp	C/G	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91091419	TGGGAATTCACCCGG[C/G]TTCCAGCCAGTGGGC	66795
rs29511431	snp	G/T	0.375	0.216506	synonymous-codon, intron-variant, nc-transcript-variant	Atg10	GRCm38.p3	13:91022608	GTCCCTGGAGCAGCC[G/T]CGGCTTATAGCACTC	66795
rs29511949	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91158497	TTATCTTAAAAAAAG[A/G]AAAAAATATGTTGTA	66795
rs29512147	snp	C/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91163786	TCTCTCTCTCTCTCT[C/G]TCTCTGTCTCTCTCT	66795
rs29512222	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91063048	AGTAAATAACATATA[C/T]TTTTATTATACTACC	66795
rs29513237	snp	A/G/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91195831	GTAATGAGATCTGAC[A/G/T]CCCTCTTCTGGTGCT	66795
rs29513310	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Atg10	Mm_Celera	13:91166722	TCAGTGCATCTTTTT[G/T]TGGAAATGGGGTAAT	66795
rs29513636	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90949860	TCCCTGTTTGTTTCA[A/G]AGTTTCATTCAGTTA	66795
rs29514113	snp	A/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90976070	GAAGTAACTCTGGTT[A/T]CCTAGGTGAGTAACG	66795
rs29514316	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90938100	GGTTTCAAAAGCTCA[C/T]GCCAGGCCCAGGTTC	66795
rs29515461	snp	A/C	0.304688	0.243945	intron-variant	Atg10	GRCm38.p3	13:91122105	GAAATGAACATTTGG[A/C]GAAAATTCAATCAAA	66795
rs29515830	snp	C/T	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:91124396	ATGTATATGCACATC[C/T]CTGAGAACATGCATA	66795
rs29515899	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91050496	GGTATCTGCATGTGG[A/G]AATGATACCCAGGTG	66795
rs29516632	snp	A/G	0.408163	0.193609	intron-variant	Atg10	GRCm38.p3	13:91088056	TTCATTTTATAATGA[A/G]TGGAATGATACACTC	66795
rs29516866	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91215792	GGGGATAATTCCGCA[C/T]CACTGACCATGAGAA	66795
rs29516885	snp	A/T	0.475309	0.108333	intron-variant	Atg10	GRCm38.p3	13:91045258	TTTGCCTTGAAATAT[A/T]TCCATATCCATAATT	66795
rs29517053	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91050115	TGGACCAAGGGGCTC[C/T]CCTCCCAGTGATGCC	66795
rs29526301	snp	C/G	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:90979126	ACTGTTATCCATCAC[C/G]GGCAGAAAGATACTT	66795
rs29527065	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Atg10	Mm_Celera	13:90936909	GAAAACAGAACTGGG[A/G]CCTTTGATTCCTCAC	66795
rs29528484	snp	C/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91022722	ACACAATGGGGCTTG[C/T]TGCTGCTCTAAAGCA	66795
rs29529350	snp	C/G	0.465374	0.126941	intron-variant	Atg10	Mm_Celera	13:91043492	TACAATGACATAGCA[C/G]AAGATGGCAAACTCT	66795
rs29530149	snp	A/G	0.456747	0.140554	intron-variant	Atg10	GRCm38.p3	13:91049004	AGTCAATCAGTTTGC[A/G]CTCTCGTGCACACAG	66795
rs29532450	snp	A/C	0.429688	0.173817	intron-variant	Atg10	GRCm38.p3	13:91140567	GGGCAGACCACTTTC[A/C]CTCAGGTTCCATTTT	66795
rs29532585	snp	C/T	0.415225	0.187619	intron-variant	Atg10	GRCm38.p3	13:91034065	TTCTGATTTCCTTTA[C/T]TCATTTCTACATTCT	66795
rs29533374	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90984514	GTGTCTGGTGAAGGT[C/T]GGCTTTTCTGGCTTA	66795
rs29534804	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91187995	ATCGAAGAGAGTCAC[A/G]TATGAGACTCCTGTA	66795
rs29535155	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90989125	AGCATGGTAACATTC[C/T]GCCAGTGGGAACCTA	66795
rs29535555	snp	A/G	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:91047467	GCACCTGTTATATCC[A/G]GCACATAAGGGGGAT	66795
rs29535957	snp	C/G	0.484429	0.0868505	intron-variant	Atg10	Mm_Celera	13:91182989	CAGCAGCTTCTCTGT[C/G]AATTAAACATGTATG	66795
rs29537909	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91218841	GCGCACGTCTTTAAT[C/T]CCAGCACTTGGGAGG	66795
rs29544558	snp	A/T	0.497778	0.0332592	intron-variant	Atg10	GRCm38.p3	13:91157234	AAAGTAAAAGCCTTT[A/T]TGCAATGGGATTGCA	66795
rs29545470	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91060056	ACAGATCCACAGCTG[C/T]AGGATCTCCATGATA	66795
rs29547263	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90997408	GAGACAACTTTGTAA[A/C]CAGAACACCCATAGT	66795
rs29547627	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90940084	ATGGGATAAGGGGAG[A/G]AGATGGGTAGTAATG	66795
rs29547977	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90949336	GCTGGTAGGTTTTGT[A/G]TGTCAACTTGACACA	66795
rs29548911	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90948103	CTGGAATTACAGAGG[A/G]GCAGGAGCCACTATG	66795
rs29549743	snp	A/G	0.492188	0.0620098	intron-variant	Atg10	GRCm38.p3	13:91156849	CAATTGCAGAATCCA[A/G]ACTAAAATTCTAGGG	66795
rs29550339	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91029781	TATAGCAGGAAGGCA[A/C]AGGAAGCTGCAGAGG	66795
rs29550646	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91106082	ACTATGATAAGCAAA[C/T]ATGTGGTAGAGGGTT	66795
rs29551043	snp	A/G	0.277778	0.248452	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90967794	AATAGAGAAGCCAAC[A/G]TCATTGGTTCTAGAC	66795
rs29551446	snp	A/C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91155691	CCCCCCCCCGCCCCC[A/C/T]CCCACACACACACAG	66795
rs29551456	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90985783	AATATTAATACCTAA[C/T]ATACACAAGCTCAAA	66795
rs29552262	snp	C/T	0.46875	0.121031	intron-variant	Atg10	GRCm38.p3	13:91011139	GAGATAAGATATAGG[C/T]TATGACTCATATGTA	66795
rs29552776	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91050385	TGTGGACATTGCATC[C/T]CTATTGGTCAGGATC	66795
rs29552867	snp	A/C	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91136744	ACACTGGTGGCCTTA[A/C]ACAGCACTGGATCCT	66795
rs29553145	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90948381	TGTAGACTCTGAAGG[A/G]TAAGAGTCTGAGCTA	66795
rs29553146	snp	C/T	0.46875	0.121031	intron-variant	Atg10	GRCm38.p3	13:91152896	AGGCAGTGAGGGCTT[C/T]CAAATACACATGAGG	66795
rs29553930	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91146256	AAGATACCTTAGAAA[A/G]CACTGACACAACAGT	66795
rs29555192	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91152498	GTGCACAAGTTTAAA[A/C]TCTGTCAAGTCACAT	66795
rs29555597	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91106165	ACACGAGGGTAGTGA[A/G]AAATAGCCTGATGTG	66795
rs29556227	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90992299	AAAGAGTCAATCACT[A/G]GGTGAGTAGGTGGGA	66795
rs29566413	snp	C/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:90977619	TTAAGCCCAGTGAAA[C/T]GCCCTAAGTAGAGGA	66795
rs29568709	snp	C/T	0.456747	0.140554	intron-variant	Atg10	GRCm38.p3	13:91170118	TCAGCTCACGGCAGA[C/T]TGCTTCACTTCATAG	66795
rs29568833	snp	A/C	0.391111	0.206368	intron-variant	Atg10	Mm_Celera	13:90950789	ATCCAGAGATGAAAG[A/C]AGTCCTTAGCTCACT	66795
rs29569342	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90953734	TGAGCCATCTCTTCA[A/G]CCACAGGGGGAAAAA	66795
rs29569924	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91046463	TAGCATTTTTAGCTT[A/G]ATGTTTTGCTTTTTT	66795
rs29570098	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91130203	ATAGACAAGGGGTCT[A/G]AGGTTTAAAAAGTTT	66795
rs29570258	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91094984	CTTCTCCCTCAGGTG[A/G]GGTGCCATGGGACCA	66795
rs29571455	snp	A/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91056764	GTTTCATGTTTAAAG[A/T]ATTGGAGAGATCTGG	66795
rs29571499	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90984832	GCCCTCATTATATTG[A/G]GAGCTGGATAGTATC	66795
rs29571749	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91060328	GAGATGAGAGGGATT[A/G]GGGTGTATGATGTGA	66795
rs29572118	snp	A/C	0.375	0.216506	intron-variant, utr-variant-5-prime	Atg10	GRCm38.p3	13:91165859	TTCTGACCTTTCATA[A/C]AGACCACGCATGGCA	66795
rs29572548	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:90936516	CCCCAGACCCGAGGT[A/G]TAGCTAAGGGTAAGA	66795
rs29572831	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91050579	TATTAGACAGGAGCA[A/G]ATTTGGATTAAAATT	66795
rs29572838	snp	G/T	0.345679	0.230967	intron-variant, upstream-variant-2KB	Atg10	Mm_Celera	13:91167472	TTCCTATCTCTAATC[G/T]CTGTTAACAGAAAGA	66795
rs29574466	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91052188	TTCAATGGATATTAA[A/C]TAGGATAGTGTATAA	66795
rs29576439	snp	A/G	0.429688	0.173817	intron-variant	Atg10	GRCm38.p3	13:91156559	TGCCTTGTGCAGACA[A/G]GCCAATGTAAAAGTC	66795
rs29584693	snp	G/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91206132	AAGTTACTGGTGTAA[G/T]ATTGACATGCAGAGA	66795
rs29584883	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91156398	GATTTATCGAACACC[C/T]ACTCTGCTTTTGGAC	66795
rs29585735	snp	G/T	0.21875	0.248039	intron-variant	Atg10	Mm_Celera	13:91071880	AAATGGCACCTAGCC[G/T]ATATAATGAATGATT	66795
rs29588024	snp	C/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91143414	GCCAGGCATGGTGGC[C/G]CACGCCTTTAATTCC	66795
rs29588280	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91185921	AAAAATCTACAGCAT[A/G]TAGAGCTGAATACTA	66795
rs29588397	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91161169	TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG	66795
rs29589192	snp	A/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91196515	TCACCCTCGGGATTG[A/T]GAGCGATGGATCAAG	66795
rs29589404	snp	G/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91148438	TTTTTTTTTTTTTGG[G/T]TTTTTGAGACAGGGT	66795
rs29610434	snp	C/G	0.33241	0.236027	intron-variant	Atg10, Gm35245	Mm_Celera	13:90963122	TTGTGGATAGCAACT[C/G]CTGGTAAAAATCTTC	66795
rs29612797	snp	A/T	0	0	intron-variant, downstream-variant-500B	Atg10	Mm_Celera	13:90937109	GTTACTGGGATGTTA[A/T]AAAAGCCCATTGTGT	66795
rs29614788	snp	A/C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:90937863	CGAGGACTGGAGAGA[A/C/T]GGCTCAGCGGTTAAG	66795
rs29617312	snp	A/T	0.290657	0.246672	intron-variant	Atg10	GRCm38.p3	13:91046352	GCATTGAAAGGATGC[A/T]TGTTTGCTTCAGCTT	66795
rs29617706	snp	C/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:90979311	TGCAGCTATGCCTCA[C/T]GATCCCAGTCATACA	66795
rs29617915	snp	A/C/T	0.277778	0.248452	intron-variant, upstream-variant-2KB	Atg10	GRCm38.p3	13:91167006	AGGGGACTAGGGAGC[A/C/T]GGCTAACTGGTGAGA	66795
rs29618850	snp	C/G/T	0.290657	0.246672	intron-variant	Atg10	GRCm38.p3	13:91129254	TGCCCTGTAGCTGTC[C/G/T]CGGGTTGATTCTCTC	66795
rs29620695	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91050217	GTCTGTGGGAGCTTG[A/C]GGGGGTGGGGTGGGG	66795
rs29620725	snp	A/C	0.345679	0.230967	intron-variant	Atg10	GRCm38.p3	13:91046451	CTCAAAACATAATAG[A/C]ATTTTTAGCTTAATG	66795
rs29623094	snp	G/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91061442	TTAAACTAACTTCCA[G/T]CAGTCTAAAATATTA	66795
rs29623701	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91069482	CAGATATGGAAAACT[A/G]TTCTCAACAATAAAA	66795
rs29630502	snp	A/G	0.444444	0.157135	intron-variant, downstream-variant-500B	Atg10	Mm_Celera	13:90936926	CTTTGATTCCTCACG[A/G]TGGCCCCAAATTTCC	66795
rs29631489	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91099941	AGATAGCCTTAGAAC[A/G]AGCTTCTCCAGCAAT	66795
rs29631951	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91004508	AGGAGAAACTTGATA[A/G]AGATTGATTCTCCCT	66795
rs29632399	snp	A/G	0.304688	0.243945	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90970369	ACGGCAAGACATGCC[A/G]GTGCTGGATGATGAA	66795
rs29632644	snp	A/C	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91099026	CCCAAAACAGTTCCA[A/C]CAATTAGGAACCAAG	66795
rs29633250	snp	C/T	0.359862	0.224567	intron-variant	Atg10	Mm_Celera	13:91094570	CTCCTGGCTTATGTT[C/T]GGTTGTGTTTTAGAG	66795
rs29634899	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91192458	GCTGAGATTAAGACA[A/G]AATTTCCAACGATTT	66795
rs29635014	snp	A/G	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:90978158	AGAAGACCTTGCTAT[A/G]TGCTCTCCTTCAGCT	66795
rs29635024	snp	A/G	0.42	0.183303	intron-variant	Atg10	Mm_Celera	13:90981365	ATGAAACAAGAAGAC[A/G]CCAACTATCTCCCAC	66795
rs29636816	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91076394	CATGAAGTCTCACCC[C/T]TAGCTAAGGAGCTGC	66795
rs29637392	snp	C/T	0.432133	0.171253	intron-variant	Atg10	GRCm38.p3	13:91044973	ACCTTCGATAGAAAG[C/T]CTCTTACATAACCCA	66795
rs29637426	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90972892	GCCATCTATCTAGCA[C/T]TAAAAGAAGTCAAGG	66795
rs29637762	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91175726	CACAGACATATGCTC[A/G]GGACACTGATTCCTA	66795
rs29639866	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91070013	GCAACCAAACAGAGT[A/G]GGAAAAGATCTTCAC	66795
rs29661000	snp	C/G	0.5	0	intron-variant, upstream-variant-2KB	Atg10	GRCm38.p3	13:91166348	GAATCAAACTGATTG[C/G]CAGGGGAAAGGAGGA	66795
rs29666484	snp	A/T	0.415225	0.187619	intron-variant	Atg10, Gm35245	Mm_Celera	13:90968010	GACTCACGTGATTCA[A/T]AGGCAAACATGAGCA	66795
rs29670839	snp	G/T	0.497778	0.0332592	intron-variant	Atg10	Mm_Celera	13:91079727	ATCTCTGGGCACTTT[G/T]CCCAGCTTAGTTTAA	66795
rs29676964	snp	G/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91030225	ACCAGATGGGTCTTT[G/T]GTGAATTGTTTTAGA	66795
rs29677955	snp	A/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:90979043	TGTTAAAAACTGGAT[A/T]TAATGAAATGCATCA	66795
rs29677958	snp	G/T	0.408163	0.193609	intron-variant	Atg10	GRCm38.p3	13:91061521	TACACAGTTGCCATA[G/T]TTATAGAAAAAAACC	66795
rs29679906	snp	C/T	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:91090850	GAATTCTATTTAAAA[C/T]AATGGGCACAGTATA	66795
rs29680460	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90992722	AGAAAGAGAGAAAGA[A/G]AGAGAGGGAGAGAGG	66795
rs29682088	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90949692	GCTTTTTAGTCATGG[A/C]GGTTTTTTTTTTTGT	66795
rs29682528	snp	C/T	0.359862	0.224567	intron-variant	Atg10	Mm_Celera	13:91183089	CCCATCAGAGCAGAA[C/T]TTTGCGCAGGTGTCC	66795
rs29682897	snp	G/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91158148	AGAAGCCCAAGGTCA[G/T]GCCGCTCAACTGAGA	66795
rs29683544	snp	A/G	0.345679	0.230967	intron-variant	Atg10	GRCm38.p3	13:91136060	GTGGGACAATACTAA[A/G]TATGACAGAGCCTCT	66795
rs29683925	snp	C/T	0.387812	0.208586	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90970985	CAGGGATGGTGTGGC[C/T]AAACTCCTTAAGCAC	66795
rs29687736	snp	A/T	0.35503	0.226867	intron-variant	Atg10	Mm_Celera	13:91185939	GAGCTGAATACTAAA[A/T]GAAGCAAGAAGGGTG	66795
rs29688234	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Atg10	GRCm38.p3	13:91166227	CGTCCCGACACGCAC[A/G]GCAGTGAACAACATC	66795
rs29709522	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:90992671	AAGAAAGAAAGGAAG[A/G]AAGAAAGAAAGAGAA	66795
rs29711207	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90947872	CTGGTCTTGAACACA[C/T]TGCACAGAAGAGGAT	66795
rs29711293	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91108461	CTCAAATGGGACATA[C/T]GTAGCAATCCTCCCC	66795
rs29714031	snp	A/G	0.345679	0.230967	intron-variant	Atg10	Mm_Celera	13:91040389	GTGTGTAGATGACTA[A/G]TGGAGGTGTTACTGC	66795
rs29717183	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91192750	GACGCAGGCACAGAC[A/G]GGTGGTTCACTGTGA	66795
rs29721601	snp	A/T	0.426035	0.177515	intron-variant	Atg10	Mm_Celera	13:91204965	AGGGCTTATCCCACT[A/T]GGGGTAAAGGCCCTT	66795
rs29723364	snp	A/G	0.375	0.216506	utr-variant-5-prime, nc-transcript-variant	Atg10	Mm_Celera	13:91223985	GCGCGCACGGGGCGG[A/G]GCGGGGAGGGACGGG	66795
rs29725250	snp	C/T	0.493827	0.0552116	intron-variant	Atg10	Mm_Celera	13:91049641	TCACTCTGTCCTGTC[C/T]TCAGAACTCCCTGGG	66795
rs29725737	snp	G/T	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91198573	CAGTGACACTGTCTT[G/T]GAGTCATTTCTGCTC	66795
rs29726232	snp	G/T	0.408163	0.193609	intron-variant	Atg10	GRCm38.p3	13:91089141	TTTCCTCCTACCAAG[G/T]GGGTTCTAATGAACA	66795
rs29726565	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91218832	GCGGTGGTGGCGCAC[A/G]TCTTTAATTCCAGCA	66795
rs29727173	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90938277	CGCTTCTTCACAGCC[A/G]TAGAATACCACTAAG	66795
rs29727450	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91102440	AGAGGGAACCAGACA[A/G]GGAAGAAGGAAGAGT	66795
rs29728885	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90972740	CAAAAGGGCCCATAA[C/T]GGGAGCCCCCTCAAT	66795
rs29728890	snp	C/T	0.429688	0.173817	intron-variant	Atg10	Mm_Celera	13:90995597	TTATTTCTGCTACTG[C/T]AATATCAACTAAGGG	66795
rs29729756	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90978891	GCTCAAAAGAAAGAA[A/G]GGGCAACTCTGGCTT	66795
rs29729894	snp	A/C	0.345679	0.230967	intron-variant	Atg10	Mm_Celera	13:91169810	AGATAGCCCACCTTT[A/C]AGGAGAGAGGGACAG	66795
rs29730339	snp	A/G	0.391111	0.206368	intron-variant	Atg10	Mm_Celera	13:90950689	AATATTTTTCAAAAG[A/G]TACTTTTCTGCCATA	66795
rs29730510	snp	A/C	0.290657	0.246672	intron-variant, upstream-variant-2KB	Atg10	Mm_Celera	13:91166833	ACTGAAATAATAAGA[A/C]AAAAAGTCAGTGAAC	66795
rs29731115	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91195830	CGTAATGAGATCTGA[C/T]ACCCTCTTCTGGTGC	66795
rs29731179	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90948528	GCTTGGCAGTTTTGT[A/G]AAGGTAGTAGATAGG	66795
rs29732431	snp	A/C	0.48	0.0979796	intron-variant	Atg10	Mm_Celera	13:90948088	TTGGATCCCTTGGAC[A/C]TGGAATTACAGAGGA	66795
rs29733627	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91163485	ATAAAAAAAAAAAAA[A/G]GGGGGGAAGTTACCC	66795
rs29735071	snp	A/C	0.359862	0.224567	intron-variant	Atg10	GRCm38.p3	13:91182073	GCAACTTTTCCTCAT[A/C]TAGAGATGATGCTCT	66795
rs29735258	snp	C/T	0.359862	0.224567	intron-variant	Atg10	Mm_Celera	13:91183053	ACACAAAGCTTTCTA[C/T]CCTCCTGCCATTCCA	66795
rs29736068	snp	A/G	0.486111	0.0821678	intron-variant	Atg10	GRCm38.p3	13:91088444	AAGAAACTAAGAAAA[A/G]AATAAGAATGAAAGA	66795
rs29737603	snp	C/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91009794	TTACCGAATGACTTA[C/G]TAAGTGCTCAGAACA	66795
rs29740296	snp	C/T	0.375	0.216506	intron-variant, utr-variant-5-prime	Atg10	Mm_Celera	13:91165960	AAAGCCAAACAGAGC[C/T]CTAGAGTCACTGGCT	66795
rs29755936	snp	A/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91061922	AATTATTTTGTGTAT[A/G]CATTAAAGGTCAAAC	66795
rs29757143	snp	G/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91059745	GTTTATAAGTCTGGT[G/T]GGATGGGGGTGGGGA	66795
rs29759431	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90949060	TGTTTACTATTTTTA[C/T]TTTATGTATGTAAGT	66795
rs29759671	snp	G/T	0.429688	0.173817	intron-variant	Atg10	Mm_Celera	13:91200514	AATATTTTTAAAGAT[G/T]TATTTGATTTTTAAT	66795
rs29760930	snp	A/T	0.456747	0.140554	intron-variant	Atg10	GRCm38.p3	13:91109070	TACTGAATTTGATTA[A/T]GGGGATGACTTGTAG	66795
rs29761774	snp	A/C	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91063455	CTCACTCAGGATGAT[A/C]TTTTCTAGTTCCTTA	66795
rs29761801	snp	A/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91158036	AATACAATGAAAGAC[A/T]GGCGATGTATCTCTG	66795
rs29762392	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90949854	AACCCCTCCCTGTTT[A/G]TTTCAGAGTTTCATT	66795
rs29764164	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91119730	CACACACACACACAT[A/G]CACACACGACAGACA	66795
rs29768773	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90972670	AACAATTATCCTGAC[A/G]AGAAATGGGTCTCTG	66795
rs29775046	snp	A/G	0.48	0.0979796	intron-variant	Atg10	Mm_Celera	13:90977697	ATAATTATAAATTAC[A/G]TGTCATCATTTATGT	66795
rs29775238	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90991450	CGTAGAACAGTCCAG[A/G]TTACTTTATATAGAT	66795
rs29776364	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91181904	TAATCCCAGCACTTG[A/G]GAGGCAGAAGCAGGC	66795
rs29776372	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90937952	CACAAACATCTGTAA[C/T]GGGATCCAACGCCCT	66795
rs29777352	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91158028	ACAAATAAAATACAA[C/T]GAAAGACAGGCGATG	66795
rs29781324	snp	A/C	0.49827	0.0293608	intron-variant	Atg10	GRCm38.p3	13:91180735	CACCAGTAAGTTAGA[A/C]ATACCTAGAACAACC	66795
rs29782347	snp	A/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:90940295	TGGCTCATCTATGAA[A/T]TTCTTAAAGAATTAA	66795
rs29782462	snp	C/T	0.475309	0.108333	intron-variant	Atg10	GRCm38.p3	13:91046741	TGATATGAATTAAGC[C/T]TAACAACTAAATCCC	66795
rs29782521	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91223693	TATAGATTATGGGGG[A/G]AGGAGGTTGTGTTGG	66795
rs29783047	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90984959	AAGAAGGAATAACAC[A/C]AGGAAAACACAAAAC	66795
rs29783071	snp	A/G	0.304688	0.243945	intron-variant	Atg10	GRCm38.p3	13:91128621	CCTCCCAGCATGCTC[A/G]TTCCGTCTTGCCCTC	66795
rs29783434	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91205567	AAAACCTGGATCTTA[A/G]ATTATGTTTTTCATT	66795
rs29783614	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91171354	GCACCAAAGAGCCCA[C/T]AGGAGCCACTCTGGT	66795
rs29783851	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91196281	AGGTCCCACAGCCAG[C/T]AGCAGGTTAAACTCC	66795
rs29784263	snp	A/G	0.429688	0.173817	intron-variant	Atg10	GRCm38.p3	13:91153864	ACATTTCCAAATGAC[A/G]AGAAAACCAGGCAAA	66795
rs29784361	snp	A/C	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91170376	TGGCAGCCAAAAAAA[A/C]AAAAAAAAAAAAGGT	66795
rs29803069	snp	A/C	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91219619	ATAACACCCCACCCC[A/C]AAAAAAACCACACAC	66795
rs29805845	snp	C/T	0.391111	0.206368	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90970381	GCCGGTGCTGGATGA[C/T]GAAACTTATCTCTCA	66795
rs29806113	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90999264	AAGGGGTCATGAAGT[A/G]TAGCTGAGGCTTGAC	66795
rs29806173	snp	C/T	0.46875	0.121031	intron-variant	Atg10	GRCm38.p3	13:90974029	CTAAGGAAAGTATTA[C/T]AGAATTTCCCAGAAG	66795
rs29806488	snp	C/T	0.432133	0.171253	intron-variant	Atg10, Gm35245	Mm_Celera	13:90966522	AATGGCAGTCAGTGT[C/T]TCCCTGGAATGACAC	66795
rs29807430	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91157967	CAAAGTGAGTTCCAG[A/G]ACAGTCAGGGCTACA	66795
rs29816477	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91076827	CATTCCCACAAGCTC[A/G]CGTTTGCTTAATACA	66795
rs29820426	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91049637	CCATTCACTCTGTCC[C/T]GTCCTCAGAACTCCC	66795
rs29821260	snp	A/G	0.493827	0.0552116	intron-variant	Atg10	GRCm38.p3	13:91116240	ATGGGAAAGGCAAGC[A/G]TTTTTAAAATTATGT	66795
rs29821974	snp	A/G	0.375	0.216506	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Atg10	Mm_Celera	13:91224038	GACACGGCAGCGGAG[A/G]AGCTCTGCCCGCGCT	66795
rs29823047	snp	A/G	0.297521	0.245442	intron-variant	Atg10	Mm_Celera	13:90982253	TCTAAATTAACCTAA[A/G]TGAAGCCCAGCTTCA	66795
rs29824238	snp	G/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90948400	GAGTCTGAGCTAGGG[G/T]AGTAGGGTCTCTGAG	66795
rs29826983	snp	A/G/T	0.375	0.216506	intron-variant	Atg10, Gm35245	GRCm38.p3	13:90962466	AAAGCTGAAAACATC[A/G/T]TCATTTTAAATTGAG	66795
rs29828622	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91071491	GCCCAAGATGATATA[C/T]TGATCAGGTTTTTAA	66795
rs29829811	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Atg10	GRCm38.p3	13:91167642	TACGGCAAATGCCCC[C/T]AAACACTGCTCCCTT	66795
rs29834336	snp	A/G	0.486111	0.0821678	intron-variant	Atg10	Mm_Celera	13:91183750	CTAATAAAAAAGAAA[A/G]AATTATATAGATATT	66795
rs29848461	snp	C/T	0.32	0.24	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90971009	TAAGCACAACACTTG[C/T]TTTCTTTGAAACCTA	66795
rs29850306	snp	G/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90978023	CAGTGACACACCTAC[G/T]CCAACAGGACCACAC	66795
rs29853301	snp	C/T	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91153338	GCCTCTGCCTTTTTA[C/T]GAAGATGCTCGGAAT	66795
rs29855126	snp	A/G/T	0.391111	0.206368	intron-variant	Atg10	GRCm38.p3	13:91097356	GATGTAGCACATGGT[A/G/T]CAGGGTACAATGATG	66795
rs29856718	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90985006	AAGAAGCTCCCTTCC[C/T]GAGTTATCTTATGAA	66795
rs29862977	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91113382	ACCCATGTGAACACA[C/T]AGAGATTGTCAGAGC	66795
rs29862978	snp	G/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91052596	ATGACTGCTTAAACA[G/T]GTCCTGATCAATTAC	66795
rs29867067	snp	A/G	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91032122	AGCTTACATAATACG[A/G]AAGCAAAGTGTGTGG	66795
rs29867431	snp	A/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91126168	GAGCAATTCTAGTTT[A/T]ACTTATTATTCTCCG	66795
rs29873899	snp	A/T	0.375	0.216506	intron-variant, downstream-variant-500B	Atg10, Gm35245	Mm_Celera	13:90972468	CTCCATGCACGTCAA[A/T]TTTTAAATGAGGTAG	66795
rs29877401	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90987878	AATATACACAGGACT[C/T]GCATGGGTCTGCACC	66795
rs29878245	snp	C/T	0.465374	0.126941	intron-variant	Atg10	GRCm38.p3	13:91091752	CCTGCTTCCTTTCCT[C/T]AGCTCCTACATACAG	66795
rs29881736	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91171294	TATGTATGTGAATTA[A/G]CATCTGCTGGTGCAG	66795
rs29884057	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90938078	GTTGGAGAAAGTGTG[C/T]GTTTGAGGTTTCAAA	66795
rs29895143	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:90994141	AGCCACCCTTCATTC[C/T]TTTACTATACCCTCT	66795
rs29898582	snp	C/T	0.375	0.216506	intron-variant, downstream-variant-500B	Atg10, Gm35245	Mm_Celera	13:90972491	TGAGGTAGATGCACT[C/T]ACTAACTAGCATGAC	66795
rs29899596	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91048313	TCCTTTGCTCGTCAC[C/T]GAGCAACTAAGACAC	66795
rs29906776	snp	C/T	0.498615	0.0262793	intron-variant	Atg10	GRCm38.p3	13:91102256	TTGGTCTCATGAGTC[C/T]ATACTAAATATGGAA	66795
rs29913152	snp	A/C/T	0.46875	0.121031	intron-variant	Atg10	GRCm38.p3	13:91034426	TTCCAAGCCCTAATC[A/C/T]GCTTTTCTGGTCATT	66795
rs29913186	snp	C/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91025209	CCATGCTTCCTCTGA[C/G]GACAGAGACACTGTG	66795
rs29914681	snp	A/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91172409	TGTTTCCACCCGTGA[A/T]CTCCTTCATCTGAGA	66795
rs29915647	snp	A/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91154043	GCTGTTTTCATTGCT[A/G]TGAAGCAACTAATCC	66795
rs29916350	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90977813	TGATCAAGGTACCTG[C/T]CATAAGAACAACATT	66795
rs29916694	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90947907	CTGGACTCTTGGACT[C/T]TTCTCCCTCTCCCTC	66795
rs29925504	snp	A/C	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91083892	TCAAAATGTGACTTT[A/C]TTTTCACTAAACCTC	66795
rs29931432	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90947247	TGAATAAATACACAT[C/T]GGTACATCTGCATAA	66795
rs29939996	snp	A/C	0.244898	0.249948	intron-variant	Atg10	GRCm38.p3	13:91119497	CCCCTATACTATCAA[A/C]GTGACCCAGGCTTTT	66795
rs29941389	snp	A/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91169745	AGACCACTATGACTT[A/T]GCAAGTTTGCAAGGA	66795
rs29942340	snp	A/C	0.432133	0.171253	intron-variant	Atg10	GRCm38.p3	13:91075824	AAAAAATAATTCTTA[A/C]AGTGTTAGGCTAGGA	66795
rs29943038	snp	A/T	0.290657	0.246672	intron-variant	Atg10	Mm_Celera	13:91009908	AACTGGTGAAAGGAG[A/T]CAGCCATGGAGCTGG	66795
rs29944756	snp	A/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90937741	TGCCACCCAGCTCGG[A/T]TGTAAGTGTGCTTAC	66795
rs29946008	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91153269	CAGACAGGAAGGGGT[A/G]CATACACATGTACAC	66795
rs29949792	snp	A/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91183171	ACTCTGTGGGGTTTT[A/T]ATGCTTCTTTATAGA	66795
rs29955719	snp	A/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91034880	GCAGAGATAAGAGAG[A/T]GAGAGAGAGCGCGCG	66795
rs29958140	snp	G/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91060246	TGTTTGCTTGTTTTA[G/T]TTTTGCTTTTTTGTT	66795
rs29963075	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91188773	TAGCGCAGACAGAAG[C/T]TGGTGCTGACAGTCC	66795
rs29965927	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90983666	AGTCTCCTTCCCAAG[C/T]TCAACAGACAGGCAC	66795
rs29967440	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	Atg10	GRCm38.p3	13:91167107	TCACTAAGCCAGAGG[A/G]GCATCAGTGCTTTCT	66795
rs29968211	snp	C/T	0.401235	0.199068	intron-variant	Atg10	Mm_Celera	13:90974613	CCCAGCTATGTGACA[C/T]GCACAGCCAAACTTG	66795
rs29975017	snp	A/C	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91029270	ATATTTTTCATACTC[A/C]GTGTAAATGTTTCCC	66795
rs29976223	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91111719	TGTAATTACATTAAT[C/T]TGTAAAAGGAAAAAA	66795
rs29977002	snp	G/T	0.432133	0.171253	intron-variant	Atg10	GRCm38.p3	13:91107130	AGGTGACCATAGACA[G/T]TATGAAAGTACAAAA	66795
rs29977838	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91064292	ACCTGAGAGGCTCTG[C/T]CAAATACAGAGGTGG	66795
rs29987770	snp	C/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90947919	ACTCTTCTCCCTCTC[C/G]CTCTCAAGTGCTGGG	66795
rs29991257	snp	A/G	0.304688	0.243945	intron-variant	Atg10	GRCm38.p3	13:91129109	CTTTCCTAATGTGAT[A/G]TAAGAGCCTGGGACA	66795
rs29997628	snp	C/T	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91051898	GATTAGTAGGTATGG[C/T]CTTGTTGGAGGAGGT	66795
rs29998353	snp	C/T	0.495	0.0497494	intron-variant	Atg10	GRCm38.p3	13:91133126	GGAGTTCTACAATAC[C/T]ACTGCCAGCCCGAAA	66795
rs30004648	snp	C/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91169830	GAGAGGGACAGATTG[C/T]TTATTACTGATCTAT	66795
rs30004716	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90949577	ATCAGCTCCTGCCTC[C/T]AGGTTCTAGTCCTGC	66795
rs30005048	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91219561	AATACTAATTGAGAG[C/T]TGGGGGTGTGTTCAG	66795
rs30005951	snp	C/G	0.465374	0.126941	intron-variant	Atg10	GRCm38.p3	13:91181133	CTGGGACCTGTTGGA[C/G]CTGGCATTCTTGTCT	66795
rs30006898	snp	A/G	0.32	0.24	intron-variant	Atg10, Gm35245	Mm_Celera	13:90966806	GGAACTTTTATTAGG[A/G]TGATACAAGTTATAT	66795
rs30012518	snp	A/C	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91067059	AAAATCAACTTTCAA[A/C]CAAAAGTCATAGAAA	66795
rs30016900	snp	A/G	0.48	0.0979796	intron-variant	Atg10	Mm_Celera	13:91034899	AGAGAGAGCGCGCGC[A/G]CACACACACACACAC	66795
rs30017472	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91123591	CCTGATACATCTAAA[A/C]CCATGGCTCCAGGAC	66795
rs30017819	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91129337	GAATAACCGTGACCT[C/T]GGCAGAATTCCAGAG	66795
rs30018768	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90951389	AATTTCACACACCGA[A/G]CTCTCCCTCACATTC	66795
rs30022410	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Atg10	GRCm38.p3	13:91166238	GCACAGCAGTGAACA[A/G]CATCCTCGGCATACC	66795
rs30024607	snp	A/C/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91189795	TTAAAAATTACTGTG[A/C/G]CAGAGGAGATTGGCA	66795
rs30024685	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91051654	AGCCTGGGCAAAACA[C/T]TAAGTTTTTAATGCA	66795
rs30028400	snp	C/T	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:91046340	GCCGCTCTTTACGCA[C/T]TGAAAGGATGCATGT	66795
rs30029434	snp	A/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91192708	TCGCAGTGCGTGGTG[A/G]CGCGCACCTTTAACC	66795
rs30038515	snp	A/G	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91072013	ATATTTGTATGAAAT[A/G]TAGTATAGAACCTGA	66795
rs30041402	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91216271	CCTAACTATGAGAGG[A/G]AAACTTCAACTTTTA	66795
rs30045520	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91103228	AACACACACACACAC[A/G]CACACACACACACAT	66795
rs30048453	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90997856	GGAAATGTGAAACAG[A/G]AGAAAATGCCCCCAT	66795
rs30052029	snp	A/C	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91082701	TTATAGCGTTCAAAT[A/C]AGAGCTGAGCCAGGC	66795
rs30052091	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91136923	GCCAGAATGCCATTG[C/T]TAAGGAGGCCCTCGC	66795
rs30052132	snp	G/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91100310	AACTTGCCAGCGGGC[G/T]AGGGGTACATGACCA	66795
rs30052170	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91191702	TATGTTTCTTCATAT[A/G]TACATTTTGTGATAA	66795
rs30054310	snp	A/G	0.473373	0.11227	intron-variant	Atg10	GRCm38.p3	13:91030728	ACTTTGCTCTCTTGT[A/G]CACATTCTCTGTTTA	66795
rs30054365	snp	A/C	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91002205	GAAAGACAGTAAGAT[A/C]CGGGAATGATGGATG	66795
rs30055273	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90973003	GCCAACCCACTTTCC[C/T]CGCTACTCATACAGG	66795
rs30056175	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90951387	ACAATTTCACACACC[A/G]AGCTCTCCCTCACAT	66795
rs30061130	snp	C/T	0.265928	0.249492	intron-variant	Atg10	Mm_Celera	13:90974294	TCACCGGGTTCTGTG[C/T]AGAGAAACTGTAGAA	66795
rs30063778	snp	G/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91076926	GAATCCAGAAGCAAT[G/T]ATATCCTAGCACCTA	66795
rs30063947	snp	A/G	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:91062102	CCCTCGGCAGCAGCA[A/G]CAATAAACAGTACTG	66795
rs30064057	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91028737	TTCTAAATTTCTCCA[C/T]GGTATGTGCTTGTCC	66795
rs30067346	snp	A/G	0.444444	0.157135	intron-variant, nc-transcript-variant	Atg10, Gm35245	GRCm38.p3	13:90969598	GAAAAGGGAAGAAAG[A/G]AAGTGTTGTGTTCTA	66795
rs30073431	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91082286	CCCATAATCCTTATT[C/T]TTTTGTTCTTAAATC	66795
rs30078153	snp	G/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91169759	TAGCAAGTTTGCAAG[G/T]ATGCATGGGGAGAGT	66795
rs30079035	snp	A/G	0.345679	0.230967	intron-variant	Atg10	Mm_Celera	13:91209048	AATTACTACTAGATC[A/G]AACTCACAAATGTGA	66795
rs30088666	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:90991745	CAGCCCTTCAAAATT[C/T]TGCATTACAAAGGTC	66795
rs30090365	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90995518	CCCACTCTTTCCCAT[A/C]GTGTGACCAGTGCAC	66795
rs30094072	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90992733	AAGAGAGAGAGGGAG[A/G]GAGGGAGGAAGGAAA	66795
rs30095994	snp	G/T	0.265928	0.249492	intron-variant	Atg10	Mm_Celera	13:90982090	GTTCTGGACATAAGA[G/T]TTTCAATTCCATTGC	66795
rs30096538	snp	C/G	0.304688	0.243945	intron-variant	Atg10	Mm_Celera	13:91109018	AGGAGACTAGGAGAA[C/G]AAGAAAACTCAAAGA	66795
rs30161568	snp	A/G	0.625	0.125	intron-variant	Atg10	Mm_Celera	13:91069764	TAGTACAAGGAGATA[A/G]GTATGGATCGATTTG	66795
rs30212101	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91069501	TCAAGGATAAAAGAA[C/T]CTCTGGTGGAATCAC	66795
rs30289444	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91137678	TTTTCACTGCAGCCA[A/G]GTGATCACATCTCCT	66795
rs30289445	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91137589	CCAAACTATCACCTC[A/G]TCTATAGAAACGAGG	66795
rs30289446	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91137507	CAATCTAAGAATAAA[C/T]GAGTAAAATGTTTAG	66795
rs30289447	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91137355	AATCAACTGGACTCC[A/G]TGGGTAAAAGCAAAA	66795
rs30289448	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91136342	GTTTCTTTACAGGAT[C/T]CTACTACTTTGTAGG	66795
rs30289449	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91136160	TTCAAATTTTTGTTA[C/T]TTTTCAACCATACAT	66795
rs30289450	snp	A/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91135844	AGTAAACCAATAAAT[A/T]ATAATAATATGCTCG	66795
rs30289451	snp	A/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91135778	ATCATTTTCATAGTT[A/T]AAAAAAATGTAATCT	66795
rs30289452	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91135723	TCTGTTTCTTTTTTT[C/T]CTTTTTCCAGTAACA	66795
rs30289453	snp	G/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91134945	CAGCCGCACCGATAG[G/T]TATTTACTTTAGAAA	66795
rs30289499	snp	C/T	0.137174	0.223093	intron-variant	Atg10	Mm_Celera	13:91159569	CTTACTTCAAACCAA[C/T]AGCTGGCTGTCTTTT	66795
rs30289500	snp	C/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91159509	GGAGCACAGAGAGAG[C/T]ATTTTTTATATTTTT	66795
rs30289501	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91159378	ATTGAACATTATCCA[C/T]GGTACTCAAATTTTC	66795
rs30289502	snp	A/G	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91159223	GGCACTAATTATAAA[A/G]TTCTGTTTTCATGGC	66795
rs30289503	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91159198	CTGTAGAAAGTGAAA[C/T]TCCTTTGTTGGCACT	66795
rs30290274	snp	A/C	0.46875	0.121031	intron-variant	Atg10	GRCm38.p3	13:91158906	AGAAATTAAATCAGT[A/C]TTATATTCCTGAAAA	66795
rs30290275	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91158883	TCCCCAACACACTGC[C/T]AGGAAAAAGAAATTA	66795
rs30290276	snp	A/G	0.495868	0.0452663	intron-variant	Atg10	GRCm38.p3	13:91158735	GAGATAAGGAAATAC[A/G]TGTGGATAAAAAGAC	66795
rs30290277	snp	A/G	0.497041	0.0383476	intron-variant	Atg10	GRCm38.p3	13:91158669	AGACTAACAGCCCAC[A/G]GAAAATGAACAGAGG	66795
rs30290278	snp	A/G	0.486111	0.0821678	intron-variant	Atg10	GRCm38.p3	13:91158214	GCAAGGTCAAAACCA[A/G]AGGACTGAAACACTC	66795
rs30290279	snp	A/C	0.46875	0.121031	intron-variant	Atg10	Mm_Celera	13:91158151	AGCCCAAGGTCAGGC[A/C]GCTCAACTGAGATCA	66795
rs30290280	snp	A/G	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91158126	CTATAATCCCTCATG[A/G]CTGGCCAGAAGCCCA	66795
rs30290281	snp	A/T	0.486111	0.0821678	intron-variant	Atg10	GRCm38.p3	13:91157709	AAAGAAATGAACAGG[A/T]AAAGTCCAGGTGCAA	66795
rs30290282	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91157650	AAGACATCTTGCTAA[C/T]CACCTGCCATAAAGC	66795
rs30290283	snp	C/T	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91157468	GGACATTGATGAAGA[C/T]CAGAGCTCAGTGGGA	66795
rs30290794	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91134928	AGAATCACAAAGGGC[A/G]TCAGCCGCACCGATA	66795
rs30290795	snp	G/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91134306	TAAGGGCCTAGCCAT[G/T]AGAGAACAAGAAATG	66795
rs30290796	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91134175	CAAAGAGAGCAGAAT[A/G]CACATGCACAGAAAT	66795
rs30290797	snp	C/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91134153	AAATATAAATTCTAA[C/G]TTTTGCCAAAGAGAG	66795
rs30290798	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91133919	TGTACACAAAAATGA[A/G]CTTAGTGTCCTCTTA	66795
rs30290799	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91133854	CTGATGCCTGTTAAG[C/T]GCATGCTCTTCATCA	66795
rs30290800	snp	A/C	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91133744	AACTAAATTAAAACA[A/C]TGCACTAATGTCCTC	66795
rs30290801	snp	A/C	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91133651	TCTCCATGAAAGACT[A/C]AAAAAACCTGCAACC	66795
rs30290802	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91133537	GCTGACACTTCTATT[A/G]GCTTAAAAAAAAATC	66795
rs30290803	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91133470	TCATATATAATTCTC[A/G]TAAGCTAAAATCTCA	66795
rs30290934	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91121806	CTAAAGCTATTATTT[A/G]TTTCATCTATGGTTG	66795
rs30290935	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91121611	ATCATGTAGCTAAGT[C/T]GAGGCTTACACTGAA	66795
rs30290936	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91121278	TCTTGAGGAGGAGAA[A/G]GCGATGGGGAGGGGG	66795
rs30290937	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91121167	CAAGAATCCTATTTG[C/T]TGCTATTTTGGTCTC	66795
rs30290938	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91120251	CTCTCGAAGCAGCTC[A/G]CCCCCTTTGATAATG	66795
rs30290939	snp	A/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91120162	GAAACAAACTCCTCA[A/G]CAAGAAGAGCTGAGC	66795
rs30290940	snp	A/G	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91120116	AAAAATTTTAACAAT[A/G]ATCCCAGCAGGTAAG	66795
rs30290941	snp	C/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91120078	TAAAGATAAACAATA[C/T]AGCCATAATTTCTCC	66795
rs30290942	snp	C/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91120046	GAACCCATTAGCTTG[C/T]ATAATTAAAATAGTA	66795
rs30290943	snp	C/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91119891	CTCACATATAGATTA[C/T]AGATTTTGACCAGAG	66795
rs30290954	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91078421	TGGCATGGCCTCATG[A/G]CACATCCTTTCTAAG	66795
rs30290955	snp	A/G	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91078410	TGTTCCAGCACTGGC[A/G]TGGCCTCATGGCACA	66795
rs30290956	snp	A/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91078335	AAGGGAACTGTCCAC[A/T]TGACTAATTTGAGAG	66795
rs30290957	snp	A/C	0.497041	0.0383476	intron-variant	Atg10	GRCm38.p3	13:91078312	TCCATTGTGTTTTCA[A/C]AACTTGAAAGGGAAC	66795
rs30290958	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91078268	AACAGCTGTTCTGTA[A/G]TAGCACATATCACAT	66795
rs30290959	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91078182	ACCAAAAAGTGCCAA[C/T]TCATCCTTCCTGTGC	66795
rs30290960	snp	A/G	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91078117	TCTTGTGACTCCTGT[A/G]CCTATATATGTGCTC	66795
rs30290961	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91077976	GGTCACAATGTCAAA[A/G]CTCTGTCCCATTTTC	66795
rs30290962	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91077936	CTATGCTCTCTCCAT[A/C]CATTACCCTAACACT	66795
rs30290963	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91077679	TATTCATTCCTGGCT[C/T]CTCAGTCTGGCATAC	66795
rs30291194	snp	C/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91157346	CTGAGTAAGCCAGAG[C/T]CAGTGCTCTAACAGC	66795
rs30291195	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91156361	CAGCACATAAATGCA[A/G]TGACTACATCATTAC	66795
rs30291196	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91155751	TAATCTATTCATCTA[C/T]TGTGGAGTATTATAC	66795
rs30291197	snp	A/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91155631	TAGAGTGACAGGTTC[A/G]GCCTATGAACTGTAG	66795
rs30291198	snp	C/T	0.46875	0.121031	intron-variant	Atg10	GRCm38.p3	13:91155440	GTTACCCAGCATTTA[C/T]ACCTTAACAGGATCT	66795
rs30291199	snp	C/T	0.495868	0.0452663	intron-variant	Atg10	GRCm38.p3	13:91155346	CTTGCTTGAATTCCA[C/T]GAATTTATACAGAAG	66795
rs30291200	snp	A/C	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91155330	CCATTTTAAGGCAAA[A/C]CTTGCTTGAATTCCA	66795
rs30291201	snp	A/G	0.46875	0.121031	intron-variant	Atg10	Mm_Celera	13:91154975	GTGTGTCAATCACAG[A/G]ACGTTCTCAGCCTCG	66795
rs30291202	snp	G/T	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91154889	GGCTCTAGTTCTGTC[G/T]GCAGGGGTCAAAGTC	66795
rs30291203	snp	C/T	0.497041	0.0383476	intron-variant	Atg10	GRCm38.p3	13:91154861	TTACACTGCACCATT[C/T]CCTAGGCTCGGTGGC	66795
rs30291384	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91098283	AGTGGATTTGATAAG[A/G]CTACTAGGAAACTCC	66795
rs30291385	snp	C/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91098183	TCCCTCTAACATGGT[C/G]GAGTAAAACCCAATC	66795
rs30291386	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91098144	ACAGAATGGTGTACG[A/G]ACTCGGAATCACACA	66795
rs30291387	snp	G/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91098124	GTATACTGAAGAGGC[G/T]TGGAACAGAATGGTG	66795
rs30291388	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91098090	AAAGAACTTGACACT[C/T]GGCATGGCCTCTGCA	66795
rs30291389	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91097890	TTGAGACATGCTCTA[C/T]AGTACTACTTGCCTC	66795
rs30291390	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91097727	TCAATCAACTGAATA[C/T]ATCTTCCCTGAGGCT	66795
rs30291391	snp	G/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91097696	CAGCTTTGGAAGGTG[G/T]AAGGTGAATGAAATG	66795
rs30291392	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91097621	AAAAATCATGTAATT[A/C]AAATACTACAGGAAA	66795
rs30291393	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91097383	GATGTTCTAGGATCA[C/T]GAGTCATAACCCTAC	66795
rs30291604	snp	G/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91133385	TTTAAATTAACCTTT[G/T]CAGTTTAACTAAGGA	66795
rs30291605	snp	A/C	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91133360	CCACAATAATACTCT[A/C]TAGAATATTTTTAAA	66795
rs30291606	snp	A/C	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91133292	CCATTCCTTTAAAGA[A/C]AGTCTGCAGGAGCCA	66795
rs30291607	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91133267	AATACCTAATGCTTG[A/G]TTTAGCAAACCATTC	66795
rs30291608	snp	C/T	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91133254	AAGGCTTATCTCAAA[C/T]ACCTAATGCTTGATT	66795
rs30291609	snp	A/C	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91133057	CAAGCAACCAGAACA[A/C]CAGCTGTCACCTGCT	66795
rs30291610	snp	G/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91132842	CTCCATGTACTAACT[G/T]CAGGTACCATGGCCT	66795
rs30291611	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91132825	GGATAACCATGACAC[A/G]CCTCCATGTACTAAC	66795
rs30291612	snp	C/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91132742	CACAGGGACATGGAG[C/G]AGAGGCTCCTCCTTA	66795
rs30291613	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91132713	CAGAGGAGAGAGTAG[A/G]ATGTGCTCAGCGCCA	66795
rs30291644	snp	C/G	0.459184	0.136902	intron-variant	Atg10	GRCm38.p3	13:91046314	GAGTTGTGGGCTCTC[C/G]GCTCTCTTGAGCCGC	66795
rs30291645	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91046249	GCTTCCGCTGCCTTC[A/G]AGCTGCCCACGCACC	66795
rs30291646	snp	C/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91046013	CTCGGTGGATTGCCT[C/G]CCTAGGGTCGGAAGT	66795
rs30291647	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91045984	GCAGTAAACAACAGC[C/T]AGAGAAGCGTCTCCT	66795
rs30291648	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91045958	CAAGGCTCCTCTCCG[A/C]GGCCACATAAGCAGT	66795
rs30291649	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91045933	ACCTTACCAAAGCTA[C/T]ACCAAGTCACAAGGC	66795
rs30291650	snp	C/T	0.35503	0.226867	intron-variant	Atg10	GRCm38.p3	13:91045823	GGCTGGCACTGCAGC[C/T]ACAACATTTTGTTCT	66795
rs30291651	snp	C/T	0.336735	0.234472	intron-variant	Atg10	GRCm38.p3	13:91045758	CTTTTAGCTCATATA[C/T]ACAAACAAGGCCCAG	66795
rs30291652	snp	A/C	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91045737	ATCTTTGCATCTCAC[A/C]CAACACTTTTAGCTC	66795
rs30291653	snp	C/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91045661	TAAAACTAAGGAAAA[C/T]TGTTTCTGGCGTCGT	66795
rs30291744	snp	A/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91118756	CCCTCAGCAACAAGA[A/T]AGCAATGGTGCTTTG	66795
rs30291745	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91118642	ATTTAGTAGCGATAG[C/T]GAGTCTTTTAAAGTC	66795
rs30291746	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91118458	ACAAAATTCAAGTCG[A/C]TTTTTTCCTTTCTCA	66795
rs30291747	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91118354	GCTGCTCAAGCTCCC[C/T]GACTATTATTTAGCA	66795
rs30291748	snp	A/G	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91117002	TTTCATTTAGTTCCC[A/G]TATACTTTATTTCCG	66795
rs30291749	snp	G/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91116960	GAAAGTCTGTATTGT[G/T]TCATATTATAAAAAT	66795
rs30291750	snp	G/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91116953	ATGGTTAGAAAGTCT[G/T]TATTGTGTCATATTA	66795
rs30291751	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91116939	TGATTATCAGTATCA[C/T]GGTTAGAAAGTCTGT	66795
rs30291752	snp	A/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91116769	AGCTCTGGACAACCC[A/T]TCAGATATTCCATGT	66795
rs30291753	snp	A/C	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91116753	GCCTCTCAGTCTCCG[A/C]AGCTCTGGACAACCC	66795
rs30291804	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91077642	CTCACTGTTCCCAGA[C/T]GGACAGGAGTCCTGT	66795
rs30291805	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91077570	GTTGGATAAGAGACC[C/T]GAGACCCTGGCTACC	66795
rs30291806	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91077556	CAACTGCCACTGTAG[C/T]TGGATAAGAGACCTG	66795
rs30291807	snp	A/G	0.489796	0.070696	intron-variant	Atg10	Mm_Celera	13:91077520	GCTCACATCAAAGAG[A/G]GGACAGCGTCTCTTC	66795
rs30291808	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91077229	TCTGTACCTGCTCTG[A/G]AACAGGTAACCATGA	66795
rs30291809	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91077144	GGAACTGGTAAGGCT[A/G]AGTGAACTCAGACCC	66795
rs30291810	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91077127	GCCACCAGGCAGACA[C/T]AGGAACTGGTAAGGC	66795
rs30291811	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91073906	TTTTCAAAACCACAG[C/T]AGTTTTGCTAGGGGA	66795
rs30291812	snp	A/C	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91073864	ATTCAAAGTAAAAAA[A/C]TTAAATGCAAATTAA	66795
rs30291813	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91073434	ATCTTTGGTTAGTTA[C/T]GCTATGTGAAGAACC	66795
rs30291864	snp	A/C	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91032254	AAATGTATTCAGGTC[A/C]AAGGACTTCCAGGCA	66795
rs30291865	snp	G/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91032062	TTCCACTGATCCACT[G/T]AACTGAGATAGCCAA	66795
rs30291866	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91032016	TGATTATGATCCTAA[C/T]TATTTCAAATTGAAC	66795
rs30291867	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91031972	TAAACCTTAGCAAAC[A/G]CTGTGGGCACATGAC	66795
rs30291868	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91031865	AGGCTGATCTGCCTA[A/G]CCATAGCTTAGCCCT	66795
rs30291869	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91031500	TTCCTCTTTAATGAC[C/T]TGCCAACTTGTAACA	66795
rs30291870	snp	G/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91031157	AAGAATTTTTTCAAT[G/T]TAAAGCTCTAGACTC	66795
rs30291871	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91030485	AACTCTGGGTTCAGC[A/G]AGAGCTGACAAGCAA	66795
rs30291872	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91029329	TTACTGGTTACCTGA[C/T]GCTGTACTCTTGCTA	66795
rs30291873	snp	C/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:91026603	TGTGGTTAGCATGTG[C/G]TAGGCCCTAGGTTCT	66795
rs30291904	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90982958	CCTTAAATGAGCTGC[A/G]TACCCAAAGGAGAAA	66795
rs30291905	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90982670	CAGATTCTATATCTG[C/T]TGACAGACACCACAG	66795
rs30291906	snp	A/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90981914	GACAAGGGAAGTTAC[A/T]AATATCATGAAGAGG	66795
rs30291907	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:90981885	ATGTGTAAGAATACA[A/G]GAACATAAGGCTGGA	66795
rs30291908	snp	A/G	0.21875	0.248039	intron-variant	Atg10	Mm_Celera	13:90981663	GCTACAGGAGAAACA[A/G]ATCCCCTCGAGAAAG	66795
rs30291909	snp	A/G	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:90981549	TTGGTTAACACAATC[A/G]GGGGTGGATTACCCA	66795
rs30291910	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:90981465	TTGTGGTCATCACAC[C/T]GACGAAAGCCTCAAT	66795
rs30291911	snp	A/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:90981160	TCACATCCTAATAGT[A/G]TTTACAATTCAGAGA	66795
rs30291912	snp	A/C	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:90981120	AAGATCCTACGTCAG[A/C]GAGAGATGCTGTCAC	66795
rs30291913	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:90981073	CATAACCTCTAAAAG[A/G]GAAGTCTCTCAACAC	66795
rs30292194	snp	C/T	0.124444	0.216185	intron-variant	Atg10, Gm35245	Mm_Celera	13:90962353	CTTCCAACATGTGAG[C/T]CTGTGCTGAAACTCC	66795
rs30292195	snp	C/T	0.444444	0.157135	intron-variant	Atg10, Gm35245	Mm_Celera	13:90962324	GTCCACAAAGGGCAG[C/T]TCCAGCATGAGGGCT	66795
rs30292196	snp	A/G	0.244898	0.249948	intron-variant	Atg10, Gm35245	Mm_Celera	13:90962292	AGACATAAAGCAAGA[A/G]TGATGCCGTTCCAAC	66795
rs30292197	snp	C/T	0.142012	0.225474	intron-variant, upstream-variant-2KB, nc-transcript-variant	Atg10, Gm35245	GRCm38.p3	13:90961464	ACCTCTCCAAGCAGG[C/T]CCTGATTTCTGTCTG	66795
rs30292198	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Atg10, Gm35245	GRCm38.p3	13:90960074	AGTGAGCAGAGTGTG[C/T]GCAGCCTCAGAAGTC	66795
rs30292199	snp	C/T	0.345679	0.230967	intron-variant, upstream-variant-2KB	Atg10, Gm35245	Mm_Celera	13:90959625	TGATCGTGTGGATTT[C/T]CAGGTGTCTCTCAAC	66795
rs30292200	snp	C/T	0.244898	0.249948	intron-variant	Atg10	GRCm38.p3	13:90959083	TTAATTAAACAGTCA[C/T]GCTGCACAAGTAGGT	66795
rs30292201	snp	C/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:90958919	CTCAAACTTATTTAG[C/T]TATCAATTTATTGTA	66795
rs30292202	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90955410	GAATTTTCTGAAGAT[C/T]TTTTTCTCTTTCATC	66795
rs30292203	snp	C/T	0.493827	0.0552116	intron-variant	Atg10	Mm_Celera	13:90954530	GAGAAATGCTTGGAA[C/T]CAGCCTCCTGAGCAC	66795
rs30292314	snp	A/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91096896	TAATAATAAGTTTTA[A/G]AATAATTCACTAACC	66795
rs30292315	snp	A/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91096866	AGAGTTTAACTTCTC[A/T]TAATTCCTATGTCCT	66795
rs30292316	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91096777	TTCATGTTAGATACT[A/G]TGCTGCCATGCTTAA	66795
rs30292317	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91096754	TCCTTATCAAAGATG[C/T]TTGCTTCTTCATGTT	66795
rs30292318	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91096724	TCCATGTCATTAGAA[C/T]TAGGCTCAGTGCCAT	66795
rs30292319	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91096648	AAACGGGTCTATTAA[A/C]AAGTCACAGATATGT	66795
rs30292320	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91096515	AGAGCTGTAGATCAT[C/T]TCCGTGCTAGGCATG	66795
rs30292321	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91096499	CTAAGGGAGCTATAC[A/G]AGAGCTGTAGATCAT	66795
rs30292322	snp	A/C	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91096446	TCTGAGTCTTTATAC[A/C]CAGCTGAAGTTGCAC	66795
rs30292323	snp	A/T	0.35503	0.226867	intron-variant	Atg10	Mm_Celera	13:91096204	AATTGAAAAAAATTT[A/T]AAATTGATGATTAAT	66795
rs30292504	snp	G/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91045599	ACAGGTCCCAGCATG[G/T]TCATTTAACTGCTCT	66795
rs30292505	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91045473	CAAAGATGGAAGAGC[A/G]GCCATGCTACTTACA	66795
rs30292506	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91045420	ATCTTGCTGATGACT[C/T]AGTAACTACTGCTTC	66795
rs30292507	snp	G/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91045394	GGGACAACCTGTGCA[G/T]ATGCATATGGATCTT	66795
rs30292508	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91045235	TTCCTTTAGTGCATC[C/T]TTTTCTCTTTGCCTT	66795
rs30292509	snp	A/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91045002	CAACTTATGTTCAGT[A/T]ATCATAAATATATTG	66795
rs30292510	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91044798	TTTGTAAATAATTTA[C/T]TGATCCTTATTACAA	66795
rs30292511	snp	A/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91044611	GCAAAGGCAAACATC[A/T]ACTTGCATGTTGATT	66795
rs30292512	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91044325	AGCTGCATGTGGGAC[C/T]CTTACTGCTCATGTA	66795
rs30292513	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91043613	TACAGCTCTGAAAAA[C/T]GGAATCCTTGCTTAT	66795
rs30292524	snp	C/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91132682	GCTCACAGCTCTACC[C/G]TGTGTCAGTGAGCAC	66795
rs30292525	snp	A/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91132642	CTGAAAGAAACTGCT[A/T]TGGGAGGACGGTTTT	66795
rs30292526	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91132529	GGTTGTGGCATAGAG[A/G]CTCGGGGATAAGATT	66795
rs30292527	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91132503	CAGAGAGGACAGGCA[A/G]TAGAAATACAGGTTG	66795
rs30292528	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91132311	GTTACAGTAGGTCAA[A/G]GAAGATGAACACCAG	66795
rs30292529	snp	C/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91131894	GTTTATTTCAAGAAA[C/G]GCTTGATTAATTTTT	66795
rs30292530	snp	A/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91131849	ATGAATAAAGAATTC[A/T]TTTCTCCCAGTGTTT	66795
rs30292531	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91131814	AACTTTTGCCATAGC[A/G]TAATTCAGTGACCTG	66795
rs30292532	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91131813	CAACTTTTGCCATAG[C/T]GTAATTCAGTGACCT	66795
rs30292533	snp	A/C	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91131773	TTCAATACTTCATAA[A/C]GACCATGGCTTATGG	66795
rs30292534	snp	C/T	0.495868	0.0452663	intron-variant	Atg10	GRCm38.p3	13:91154804	CACTTCCTTATGGTG[C/T]CTCCCAACATTCTGT	66795
rs30292535	snp	C/T	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91154678	CTGGGAGATTTGAGG[C/T]TTCACAGCAAGGCTG	66795
rs30292536	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91154561	TTTTCAATCTACTAG[C/T]CCAGCACACTGAGGT	66795
rs30292537	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:91154467	AATGTACACTGTGTA[C/T]TACTTGATAAATATC	66795
rs30292538	snp	A/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91154371	ATGCAAGAACCCATC[A/G]CTTGAAGAACTACCA	66795
rs30292539	snp	A/G	0.375	0.216506	missense, intron-variant, nc-transcript-variant	Atg10	GRCm38.p3	13:91154257	CTGGCATGTGGTGTC[A/G]AGGTCTCATTCTTTA	66795
rs30292540	snp	A/G	0.486111	0.0821678	intron-variant	Atg10	GRCm38.p3	13:91154191	TGAAGACTGAAAAGG[A/G]GCTCATGGCACACGA	66795
rs30292541	snp	C/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91154095	CCTACTGCCAACAGT[C/G]CCAGGATCCAAGGGC	66795
rs30292542	snp	A/G	0.5	0	intron-variant	Atg10	GRCm38.p3	13:91154063	GCAACTAATCCCTCA[A/G]GAATGAAGCTCACAT	66795
rs30292543	snp	C/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91154012	ACTGAAGGATCACAG[C/T]ATATACACCACAATT	66795
rs30292574	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91116673	CTCAGAACTAGGTAG[A/G]CCCACATCAGGAAGC	66795
rs30292575	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91116538	TCATCTGCACTGTGC[C/T]GGTACTCCTTACGTG	66795
rs30292576	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91116333	CATCCCAATCCTAAG[C/T]CTTAAGGTCACCCAG	66795
rs30292577	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91115563	AAAATATTGAAGACA[A/G]ATGATAAACAGGCAG	66795
rs30292578	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91115331	TAATTTAAAAAAGCA[A/G]GTGGTAACCAGATGT	66795
rs30292579	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91115273	GCCAAGAGATCCTAG[A/G]ATGAAGGCCCTGAAA	66795
rs30292580	snp	A/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91115160	ACATCAGCCTTCTTA[A/T]CTAAGTCATTTGGGA	66795
rs30292581	snp	C/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91115149	TAGTTCTCCAGACAT[C/G]AGCCTTCTTATCTAA	66795
rs30292582	snp	A/C	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91115043	CCCTGGTCTCAAGGA[A/C]ATTTTATACTGAATC	66795
rs30292583	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91114986	CGCTGTTTCCAGATG[C/T]GACATATTATATTCA	66795
rs30292634	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91073373	GAAGTGGAAAGTGTA[A/C]CCTACAATAAAACAG	66795
rs30292635	snp	A/C	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91073323	GTACAGTACCCACGA[A/C]AGTCCCATGTGGAAA	66795
rs30292636	snp	A/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91073321	CAGTACAGTACCCAC[A/G]ACAGTCCCATGTGGA	66795
rs30292637	snp	A/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91073181	AGTTTTTAAAATGTG[A/G]CAATTTATAAAAGGT	66795
rs30292638	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91073158	TGGCAATAAGAAATG[C/T]TACAACCAGTTTTTA	66795
rs30292639	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91073071	AAATGGGTAATGAAC[A/G]TATGATACCACAATG	66795
rs30292640	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91073029	TCAAACATGCTAAAA[C/T]TTTGGACATACACTT	66795
rs30292641	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91072988	ATATGTAAGACTGTT[A/G]TATTAAGGAGATAAG	66795
rs30292642	snp	C/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91072926	TTTGTCCTTATAAAA[C/G]TAGGAATTAAAGACA	66795
rs30292643	snp	C/G	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91072715	TGGAGGTGTGAGGCT[C/G]TGGTTCGGTAGTAGA	66795
rs30292824	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91023871	AAACTTTGCTTTCTC[A/G]TCTTCAGTTACTTTT	66795
rs30292825	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91023639	TCAAGTCTGCCTCAA[A/G]AGAATACATCATATA	66795
rs30292826	snp	C/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91023490	AGAGGAAAAATAGGT[C/G]GGAGAGATAGTTGCA	66795
rs30292827	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91021375	GGCAGTAATAATGGC[A/G]TGATTGACAGGCCTG	66795
rs30292828	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91021039	TGGGAGACATCAGAG[C/T]GAAGGAAAGACATAA	66795
rs30292829	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91020976	AAGCGCAGGCAGCTA[A/G]GGATGCGAAGCTCTG	66795
rs30292830	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91020707	GTAGAAGTACCCAGA[C/T]AGAAGGGAGAGAGCA	66795
rs30292831	snp	A/G	0.5	0	intron-variant	Atg10	Mm_Celera	13:91020569	CATCAGCCCTATACA[A/G]TTTACATATCAAATT	66795
rs30292832	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91020165	CATCCACATTTTGCA[C/T]ATGATCTTCCTGTAT	66795
rs30292833	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91019852	GAACAGAGACGTGTG[A/G]AATTGAAACACAAAA	66795
rs30293004	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90980722	GCTACATACTATCAA[A/C]CTGATGTTCAGTAAA	66795
rs30293005	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90980479	TACCCTGAGAGGAGA[A/G]TCAAAATCCATAGCC	66795
rs30293006	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90980418	ACCCCACCGCTTCCC[A/G]AAGTTGCCCAGTCTT	66795
rs30293007	snp	A/G	0.408163	0.193609	intron-variant	Atg10	Mm_Celera	13:90980369	CTTTCTTGACCTGGC[A/G]TACATCAGCATCTGA	66795
rs30293008	snp	C/T	0.408163	0.193609	intron-variant	Atg10	Mm_Celera	13:90980343	CCTGTTTGCCCCAGA[C/T]TCCACTTCACCTTTC	66795
rs30293009	snp	A/T	0.408163	0.193609	intron-variant	Atg10	Mm_Celera	13:90980296	AGTTACCACAAGCTA[A/T]GATTGTCTCAGAAAG	66795
rs30293010	snp	A/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:90980014	TCAGAAGCACCATAC[A/T]GGGAGCTCCTCTCCA	66795
rs30293011	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90979978	GTGCCTGCCTTGAAC[C/T]TGGTGGTCACAAGTA	66795
rs30293012	snp	A/C	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90979949	GGAGTAGGGTTAATT[A/C]TCTCCCTGTTTCTGT	66795
rs30293013	snp	A/G	0.408163	0.193609	intron-variant	Atg10	Mm_Celera	13:90979924	TTAGAATCTTATCCC[A/G]TGACCAGCAGGAGTA	66795
rs30293054	snp	C/T	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91096173	TCATACTTATAACTG[C/T]GTACATTGTGATAAA	66795
rs30293055	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91096167	TATGTATCATACTTA[C/T]AACTGTGTACATTGT	66795
rs30293056	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91095889	CATCGCTTTACCAAG[A/G]AAGTGACTTCTATAT	66795
rs30293057	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91095339	GTTCTGGAGCTACAA[A/G]TTAGCAGGCTTAGAC	66795
rs30293058	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91095248	GTACAGCTCAGAAGA[C/T]CTAACAGCGATTCTT	66795
rs30293059	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91095107	ACTGCTGAGCTTGTA[C/T]CTTTTGAGCAAGACT	66795
rs30293060	snp	A/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91094336	TGGGCAGGAGGGAAC[A/G]TCCTCTGTTACTGAC	66795
rs30293061	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91093936	CAGACTGTTCTTTGT[C/T]ACTTCCTTATGTCCT	66795
rs30293062	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91093441	ACAGCCAGGCTAGGA[A/G]CTCACCGTGAACTCA	66795
rs30293063	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91093233	CACAGTGAAAATATA[C/T]AATCAATGGATGATT	66795
rs30293164	snp	C/T	0.396694	0.202437	intron-variant	Atg10	Mm_Celera	13:90953918	ACCCTGGTATTTCAG[C/T]TATGTTTGCTGCTGC	66795
rs30293165	snp	A/G	0.42	0.183303	intron-variant	Atg10	Mm_Celera	13:90953902	CCTTGCTTATGTGCT[A/G]ACCCTGGTATTTCAG	66795
rs30293166	snp	A/G	0.444444	0.157135	intron-variant	Atg10	GRCm38.p3	13:90953167	GTGAAAAGAATATAG[A/G]TTAAAAACCAATACA	66795
rs30293167	snp	A/G	0.46875	0.121031	intron-variant	Atg10	GRCm38.p3	13:90953116	CTAATATTGCTATTG[A/G]AAAATAATTTCACTC	66795
rs30293168	snp	C/T	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:90953044	TTATTATATTTATTT[C/T]TGATCACACTGTCTG	66795
rs30293169	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90952508	CACACTGTCTCATTA[C/T]ATCACATTAGTTAGC	66795
rs30293170	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90951759	CATCTGGCCAGAGCT[A/G]ATGTTTAGGAGAGCT	66795
rs30293171	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90951748	AGCTCCTCCTACATC[C/T]GGCCAGAGCTAATGT	66795
rs30293172	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90951707	CAAAGGCCTTCACAC[C/T]ACCAGTCTTGTTGCT	66795
rs30293173	snp	C/T	0.48	0.0979796	intron-variant	Atg10	Mm_Celera	13:90951677	CTTATGCTTAGGCCA[C/T]GCCTGTAATGAGGGC	66795
rs30293254	snp	A/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91131540	TCTGGTTCTCCATCC[A/T]CATCTAAAGACTCCA	66795
rs30293255	snp	G/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91131478	AGGTGAAGAAGAAGG[G/T]ATAGACAAGGAGCAG	66795
rs30293256	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91131431	GCCACAAGCCATCCA[A/G]AAGACTCACCAGATG	66795
rs30293257	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91131402	TTGCTGCTGGCCAAC[A/G]CTGGCAATAGCCAGC	66795
rs30293258	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91131359	TTCCACTCAACTGCT[C/T]CCCAATAGCTCTGAG	66795
rs30293259	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91131067	ATTTTGTTTTAATAT[A/G]CTTTGTCACATCTAC	66795
rs30293260	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91131039	TTAGGTCTCTGATAC[A/G]TAGTTGATTGAAATT	66795
rs30293261	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91130762	GAGTAGCTGGCATCG[A/G]CATAGGAGGAGGCTG	66795
rs30293262	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91130502	AGATCTGTTTCACAA[A/G]CTGATTGGTTTCAGA	66795
rs30293263	snp	A/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91130472	ATAATGGAGTCGAAG[A/T]GTAGCTCAGGAGTCA	66795
rs30293334	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91153908	CAAAGTTAGATCTGT[A/G]TAGGCTGAGACATCA	66795
rs30293335	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91153839	CTAAAGGATAAGACC[C/T]GGATTCTACACATTT	66795
rs30293336	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91153499	TGGAGCCACTGAAGC[A/G]AGCTATGGATTCTGT	66795
rs30293337	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91153397	CTGAAGCAATGAGTT[C/T]CCATCAGTCATCTTC	66795
rs30293338	snp	C/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91152534	TCGGCCTCTCATACT[C/G]TCACAGCACTTTAGT	66795
rs30293339	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91152336	CAAAGCGCCAATGGC[A/G]GAACGCTGCAAGGAT	66795
rs30293340	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91150110	TCTGGGTACCAAAGC[A/G]AAGATGGCATGTCAC	66795
rs30293341	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91150033	AGAAACCTAAGGAAT[C/T]CTCTCAAAATGACTC	66795
rs30293342	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91149902	ACTGACAAAAGGATG[C/T]ATTAGGTACTGGCCC	66795
rs30293343	snp	A/C	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91149804	GGGTTTACCTGTGAG[A/C]AATTCCGGGAGCTAA	66795
rs30293384	snp	C/T	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91043584	TGTGGAGAAGAGGTA[C/T]ATATGGGTGTGCCTA	66795
rs30293385	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91043516	AAACTCTCTGTAAGT[A/G]AAAATCTGAAGGACC	66795
rs30293386	snp	C/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91043014	AGTTCTTTCTCTTTG[C/G]TTCACAACTGGGTTA	66795
rs30293387	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91042975	CCACAAGTATCAAGA[C/T]CTGTTGCAATAAATT	66795
rs30293388	snp	C/T	0.48	0.0979796	intron-variant	Atg10	Mm_Celera	13:91042778	GTTCCCTGGGAGACA[C/T]TACAGCACATACAGT	66795
rs30293389	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91041751	AGGCTGCTTCTTTCT[C/T]ATCATACATGAATTA	66795
rs30293390	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91041682	TTAATTAAACAAGGC[C/T]GTGTAAGCAGAGATG	66795
rs30293391	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91041623	TACAGCTCAACAATA[A/C]ATCTTGATTTAGGGA	66795
rs30293392	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91041187	TTGAGTTCTAGGTAA[A/G]CAGTAATGCCAGAAA	66795
rs30293393	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Atg10	Mm_Celera	13:91040950	CACCGCTGCAGGTCT[C/T]GTCACTTCAGAATCA	66795
rs30293474	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91072687	GTTCAGTAGAGAAAT[A/G]GTACCTATCATGTGG	66795
rs30293475	snp	G/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91072642	TAAAATAAAATTTCT[G/T]AGACTAGAACCTGGA	66795
rs30293476	snp	A/G	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91072186	TGATACACTAGGTAC[A/G]TAGAATTCATGTCGT	66795
rs30293477	snp	C/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91071937	TAATCTGGGTAGAAG[C/T]CATGGAAAGAAAGAT	66795
rs30293478	snp	A/T	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91071882	ATGGCACCTAGCCTA[A/T]ATAATGAATGATTCT	66795
rs30293479	snp	A/C	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91063241	GAATCTAAGGGGAAA[A/C]GAAAAAGAGTTGGTA	66795
rs30293480	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91062194	GGACCTGACATTAAC[A/G]GGTAAAAGTTTAACA	66795
rs30293481	snp	A/C	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91062086	GGAAGCAGAAAGAGA[A/C]CCCTCGGCAGCAGCA	66795
rs30293482	snp	C/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91062037	AAACAAAAACCTTAG[C/T]CAAGACATTAACCTG	66795
rs30293483	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91061996	AAATATCTTAAGTCA[C/T]TACCAGTTTCAAAAA	66795
rs30293504	snp	G/T	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91114894	GAAAACTGAAATAAA[G/T]TTTTCCCTCCAGCTA	66795
rs30293505	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91114857	TCTTTTCCTGGCTAC[C/T]ATGAGAAACCAGCTT	66795
rs30293506	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91114834	CTTCCTCTCCCTAAA[A/C]TCCTTCCTCTTTTCC	66795
rs30293507	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91114107	AGTAGTCAAAGAATC[A/G]GAGAAAACAGATTTG	66795
rs30293508	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91113852	TATGAAAAACACAGG[A/G]GTCCATTAACTGAAT	66795
rs30293509	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91113821	ACTAAATAAAATCAA[C/T]GCATATGTATACATA	66795
rs30293510	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91112877	GTATTCAGACAAGTA[C/T]GGTCAAAGGCTTCCT	66795
rs30293511	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91112130	TTATTTCTAGGTTTT[C/T]AAATCAATACATCTA	66795
rs30293512	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91111801	ACTAAACCATGAAAA[A/G]TATTTGTAATCCTGT	66795
rs30293513	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91111769	TATTTTGGTATGTTA[A/G]AAATATAAGAACAGC	66795
rs30293554	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91019130	TGTAATTCTGCAAAA[C/T]GATGACTACTATTTG	66795
rs30293555	snp	C/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91014018	GTAATTACAGACTTA[C/T]ACTTACATTATTCAG	66795
rs30293556	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91012960	TGCAGATCCTTGTGT[A/G]TCATCTGTATAGGAA	66795
rs30293557	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91012632	AAAAAGAGATATTGC[A/G]GCCCAAGCAATCAAC	66795
rs30293558	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91012437	CCTCCAAAATGGTAA[C/T]CCCAGCAAGTTTTGT	66795
rs30293559	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91010977	CTAATCAGTATGCTG[C/T]TTCATAGTTCCACCT	66795
rs30293560	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91010964	GCAAGGAAGAAAACT[A/G]ATCAGTATGCTGTTT	66795
rs30293561	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91010353	CCAATGACTTCCTGC[A/C]GCACTGAGAGTCAAG	66795
rs30293562	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91010248	ACTTGAGCACTTACA[A/G]TTCTTACTAGAGGAA	66795
rs30293563	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91010236	CAGTGGCGCTTCACT[C/T]GAGCACTTACAATTC	66795
rs30293904	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90979880	CAAGGTTGAGCATGA[C/T]CAAAACATGGACATC	66795
rs30293905	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90979498	TGGTGAGAAGCAACC[A/G]TACTGTTGGCTCCAG	66795
rs30293906	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90979420	ACAGATAGAAGGTCA[C/T]CTTGTAGGAGCTGGA	66795
rs30293907	snp	A/C/T	0.231111	0.249285	intron-variant	Atg10	GRCm38.p3	13:90979404	AAACAAGATGGAAGT[A/C/T]ACAGATAGAAGGTCA	66795
rs30293908	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90979363	GAGAGCTTAATTAGC[A/G]TTCTCAGGGTTTTAT	66795
rs30293909	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:90978630	TTTAGGGACAATTTT[A/G]TATCACTGAAAATCA	66795
rs30293910	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90978190	CCAGTTTTCCTGTGC[C/T]TTCCCACAAGAGCAA	66795
rs30293911	snp	A/G	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:90978121	TGTAGATGAACACAC[A/G]TTGTCCCCATCCTCC	66795
rs30293912	snp	A/C	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:90977704	TAAATTACATGTCAT[A/C]ATTTATGTTGTTTAG	66795
rs30293913	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90977519	AAGTGGCTCTTCCCA[A/G]ACAATGCATACAATT	66795
rs30294024	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90951655	GCTTTGTGGTCCCCA[C/T]GGTGAGCTTATGCTT	66795
rs30294025	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90951643	GCATCAAGAAGGGCT[C/T]TGTGGTCCCCACGGT	66795
rs30294026	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90951618	AAAAATGGAGAGAGG[A/G]TTTTCCTCAGCATCA	66795
rs30294027	snp	A/C	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:90951405	CTCTCCCTCACATTC[A/C]TAATCCAAACCGATC	66795
rs30294028	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:90951357	ATTCTCTTGGCTCTG[C/T]GGGAGGGCTCAAATA	66795
rs30294029	snp	A/G	0.497778	0.0332592	intron-variant	Atg10	Mm_Celera	13:90951099	ACAACTCTGCTAGAC[A/G]GCTTCCCGTGCAAAT	66795
rs30294030	snp	A/G	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:90951011	GAGCAACCGGGCACA[A/G]AGCAAACCGTCCTTA	66795
rs30294031	snp	A/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:90950125	GCTCAGGCTGTTTCC[A/T]TTTTGGTTGTGAGCC	66795
rs30294032	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:90948796	CTACTGCTATGAGTC[C/T]GTACACATGCTGGGT	66795
rs30294033	snp	A/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:90948742	TCATGCAGTGGGCCA[A/G]CTGGTGATACCCGAG	66795
rs30294174	snp	C/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91130412	GTAGAGTCTTCAAAT[C/G]TGATGCATGGAATCA	66795
rs30294175	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91130392	CCATCACGACAGGCC[A/G]AAGGGTAGAGTCTTC	66795
rs30294176	snp	A/C	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91130118	CATTTGCATTATTTC[A/C]AGAACAGAATAAATG	66795
rs30294177	snp	C/T	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91129805	TAAACCTTCCACTTT[C/T]ATTACAGCATTAACA	66795
rs30294178	snp	A/G	0.197531	0.244432	intron-variant	Atg10	Mm_Celera	13:91129721	TTTAAAGTTTCTTTA[A/G]ACTCTTACTATAATA	66795
rs30294179	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91129690	AAACCTGACAATGAG[A/G]AGGCTATGTAATAAT	66795
rs30294180	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91128500	CTGAATATAGTTAAT[C/T]GCGTGGTTTTACTTG	66795
rs30294181	snp	C/T	0.297521	0.245442	intron-variant	Atg10	Mm_Celera	13:91128443	AAAACAGCCAAAATA[C/T]AAACAATCTATGCTA	66795
rs30294182	snp	C/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91127887	TGTATATAGCTAGTA[C/G]TATACAAAGACATCT	66795
rs30294183	snp	C/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91127833	ATTCAGTATGCAGAA[C/G]TAATAGCTTATAAAT	66795
rs30294194	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91093152	AAGGTTTACAGAAGC[A/G]AACTGCATAAATAAG	66795
rs30294195	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91092927	TGAGAAACCTTCCTT[C/T]CAACATTCACTTAGA	66795
rs30294196	snp	A/G	0.32	0.24	intron-variant	Atg10	GRCm38.p3	13:91091223	AAATTTCAAGAGAAG[A/G]AAATTTGTATTTATT	66795
rs30294197	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91089038	AACCCCTCTGAACTC[A/G]ATTCTTTTTAACGTG	66795
rs30294198	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91088603	ATCATTCTCAACATA[A/G]TCACCTGCAAGACTT	66795
rs30294199	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91088536	GACCCACACCCGAGG[C/T]GCTCCAGAAGGAACC	66795
rs30294200	snp	A/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91088412	AAGCAGGTAATATTA[A/T]AGTGAAATACAGATA	66795
rs30294201	snp	G/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91088206	GTGTGTGTGTATGGC[G/T]TCCTAGTTTTTCTTT	66795
rs30294202	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91088019	TCTCTCTCTGTCTCA[C/T]ACCCACCTTTCTTTG	66795
rs30294203	snp	G/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91087832	AATGCATGGTCTGAA[G/T]AATTTCATAACTTGG	66795
rs30294474	snp	C/T	0.124444	0.216185	missense, nc-transcript-variant	Atg10	Mm_Celera	13:91040937	TAATCACTTCTGCCA[C/T]CGCTGCAGGTCTCGT	66795
rs30294475	snp	A/G	0.489796	0.070696	intron-variant	Atg10	Mm_Celera	13:91040359	TCACAGCATATCGAG[A/G]CACTGAGGCATGAGG	66795
rs30294476	snp	C/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91040355	TAGATCACAGCATAT[C/G]GAGGCACTGAGGCAT	66795
rs30294477	snp	G/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91040327	GTGTCCACCTTCTTG[G/T]CAGGCAATGCGTTAG	66795
rs30294478	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91040246	CCAGGGCATACCCAG[A/C]CATCTCCAAGCTGCA	66795
rs30294479	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91040141	CAAATGCAAACTGTT[A/G]CCGAGAAAGGCATGC	66795
rs30294480	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91040114	CTTAGCTATCCAGAA[A/G]TTAGTAGTCTGCAAA	66795
rs30294481	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91040010	AACAATATAAAGCAG[C/T]GAGTGATTAAACCCA	66795
rs30294482	snp	A/G	0.48	0.0979796	intron-variant	Atg10	GRCm38.p3	13:91039953	TGTTTTAAATCGTAA[A/G]TGCTTGTAAAACTGC	66795
rs30294483	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91039927	CCAGGGATTCTCTAA[A/G]AATTTGCTCTTGTTT	66795
rs30294604	snp	G/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91148777	AAAAGTTGAACAAGT[G/T]TTTTATGTGTTATTT	66795
rs30294605	snp	A/C	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91148687	AGTATTAAACATTAG[A/C]TATAGGATTCTCAGT	66795
rs30294607	snp	G/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91142994	ACAATTAAAAATAAA[G/T]CATTAGTGGTCCTGG	66795
rs30294608	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91142942	TGTTTGCTGTTATGA[C/T]CCACATTAGGAAATC	66795
rs30294609	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91142839	CTTGAGGTCAGAAAA[C/T]TGAGGTTTATATAAG	66795
rs30294610	snp	C/T	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91142717	ACAGAAACAAAATGT[C/T]ATGTGCTCTCCTTTT	66795
rs30294611	snp	A/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91142643	ACTGCTGGCAACTGT[A/G]CCTGAGGAGGGGCTC	66795
rs30294612	snp	A/C/T	0.152778	0.230321	intron-variant	Atg10	GRCm38.p3	13:91142498	TGATGAAGAAAAAAG[A/C/T]TATACAAAAGGAGAA	66795
rs30294613	snp	A/C	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91142348	TTCTACTCTATCACA[A/C]ATGTAAGCAAGCTAT	66795
rs30294634	snp	A/C	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91009825	TGTACAAACTGAGAT[A/C]CAACAAATTAGCAGC	66795
rs30294635	snp	G/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:91009799	GAATGACTTACTAAG[G/T]GCTCAGAACATGTAC	66795
rs30294636	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91009762	ACAGGTACAGCATTG[A/G]GCCTCCATAAACTTG	66795
rs30294637	snp	G/T	0.46875	0.121031	intron-variant	Atg10	Mm_Celera	13:91009756	TGAAAGACAGGTACA[G/T]CATTGAGCCTCCATA	66795
rs30294638	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91009395	ATCCATGGCCATCAA[C/T]GACTCGATAAATACT	66795
rs30294639	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91008850	AGTGGTCAGAAACTT[C/T]GGAAAGTTCAAGCTG	66795
rs30294640	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91008772	CAAATCTGAGAAATT[A/G]CATCAATGAGACTAA	66795
rs30294641	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91008649	AACTATTAGGCAGCA[C/T]CTTGTTTTTATTGTT	66795
rs30294642	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91008622	TCTGCTCAACTAGGT[A/G]CATGGAAAACAAACT	66795
rs30294643	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91008233	CACTCCTTTCTCTCC[C/T]GATCCCGTGCCACCT	66795
rs30294684	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91061973	GTGAATGTGAGTGAA[C/T]GTGAAGCAAATATCT	66795
rs30294685	snp	A/G	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91061620	ACTGCCTTCCTGTAA[A/G]GCGTTCTTGTGCCTC	66795
rs30294686	snp	A/C	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91061590	AAGTTGTCATTAAGA[A/C]GCATCTGCCACTTTA	66795
rs30294687	snp	A/C	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91061477	AGTGATTTCATTTAT[A/C]AGTTCTAACATCTTT	66795
rs30294688	snp	C/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91061378	CAAGGAATTTATTTG[C/T]ATAGTAAGAAAAATG	66795
rs30294689	snp	C/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91061012	AACAGGTATGCCCAA[C/G]CTGACAAGTGACAGC	66795
rs30294690	snp	C/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91060956	GCAAACATGCAAGCC[C/G]AGGCCACTACATGGT	66795
rs30294691	snp	C/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91060884	GTGTCTTTCTGCTAC[C/G]AGCAACAATTTCTTT	66795
rs30294692	snp	C/G	0.35503	0.226867	intron-variant	Atg10	Mm_Celera	13:91060774	CATCACTGAGGACTG[C/G]TCACCAGCCATCTGG	66795
rs30294693	snp	A/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91060519	AAAGTGATAATTTCA[A/G]GAGATGCAATTAGAC	66795
rs30294694	snp	A/G	0.35503	0.226867	intron-variant	Atg10	Mm_Celera	13:91110217	TTCTTTCTCTTTCCC[A/G]TTACTTCATCCTGTC	66795
rs30294695	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91110078	TCATCCTTTGTAAAA[C/T]ACAGTAAGAACTGGC	66795
rs30294696	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91110039	CTTCTTGTGGGACCT[A/G]AAAAAAGGGTTTCTT	66795
rs30294697	snp	A/C	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91109994	TCAACCAGCTAGAGC[A/C]TCAATTAGGCTCATA	66795
rs30294698	snp	G/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91109379	GTCAGGGTTCATACA[G/T]AGGTTTAGTTTTTTA	66795
rs30294699	snp	C/G/T	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91108929	TGTGAGCACATTCCA[C/G/T]GGCAGCATGCTCCTC	66795
rs30294700	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91108432	ATATTTGGTACACTA[C/T]CCTCGTTTCTTCTCT	66795
rs30294701	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91108189	CTCTGGACCAGAGAG[A/G]CCATCATCAGGGACT	66795
rs30294702	snp	A/C	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91108050	TTGTTCTTCAGATCT[A/C]GTTTGTCTCTAGGAG	66795
rs30294703	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91107899	ACCATGGAAGGAAGC[A/G]GCTAGACTTGCCGCC	66795
rs30295174	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90976577	TTCTATCAACACTAA[A/G]CATTGATTAAGCCTG	66795
rs30295175	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90976542	AATTTTATTTCTATC[C/T]TTGGTGCTTCGATTT	66795
rs30295176	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90976211	GAAGCTACGAATTCC[A/G]TGTCTGCCACCTGGT	66795
rs30295177	snp	A/G	0.459184	0.136902	intron-variant	Atg10	Mm_Celera	13:90975876	TTCTCAGCATGCCTT[A/G]AATTAGTCTAATGAA	66795
rs30295178	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90975535	ATAGCTTCAGGTTGT[C/T]ATCATCTTCATTCTT	66795
rs30295179	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90975487	TCTGAAGCTTGTGGC[C/T]TTCTCAGTTCCACCA	66795
rs30295180	snp	G/T	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:90975449	CCCAGTAAAAGGCAG[G/T]AAAAGACCAACATCT	66795
rs30295181	snp	A/G	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90975191	CTGAATGTAGTCTCT[A/G]ACAAACACATATACT	66795
rs30295182	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:90974551	GGAAGTTGCTGTATC[A/C]AGTGATAATGGGTTA	66795
rs30295183	snp	A/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:90974431	ATTATTGTGGTATTA[A/T]AAAGAATGTGTCATT	66795
rs30295244	snp	C/T	0.297521	0.245442	intron-variant	Atg10	Mm_Celera	13:90948695	GATTATGGGGTATAG[C/T]GGTTAAGGTCAAGCT	66795
rs30295245	snp	A/T	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:90948649	GCATTTAGAAGGAGT[A/T]GTATCTGAGGAGTTT	66795
rs30295246	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90941038	TTGGACACAACCTCT[A/G]TCAACCTGTAAACTA	66795
rs30295247	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90940977	CCATATATTAACCAG[C/T]GGCAAAAAAGGGAGG	66795
rs30295248	snp	C/T	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:90940947	AATAGGATCTTAAGT[C/T]TGAGGGTACTTCACC	66795
rs30295249	snp	C/G	0.396694	0.202437	intron-variant	Atg10	Mm_Celera	13:90940922	GGAAATGAAAGCCAA[C/G]ATGGACTTGAATAGG	66795
rs30295250	snp	A/C	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:90940478	ATCAACAACCAGAGG[A/C]AAACGACATTTTTGA	66795
rs30295251	snp	C/T	0.408163	0.193609	intron-variant	Atg10	Mm_Celera	13:90940434	CTGCCAAACATCAGT[C/T]TCATGCAAACTATTT	66795
rs30295252	snp	C/T	0.5	0	intron-variant	Atg10	Mm_Celera	13:90940433	ACTGCCAAACATCAG[C/T]TTCATGCAAACTATT	66795
rs30295253	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:90939887	TGTACAGGGCTGTTT[C/T]TATAACTGAAATACC	66795
rs30295384	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91087765	CTGGAATTTACAAAG[A/G]AGGAAACAGTCTAAT	66795
rs30295385	snp	A/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91087710	CAAGGAACCAAGAAA[A/G]ACAAAAGGATTTATA	66795
rs30295386	snp	C/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91087676	ATTTACTTCTAGGAG[C/G]ATTATATGTGGCTTT	66795
rs30295387	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91087312	TTAGTAATTCCAGCA[C/T]TAATATCCTAGAAGC	66795
rs30295388	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91087247	TTCCTCAAACTCATG[C/T]TACTCCTGCCTATGT	66795
rs30295389	snp	A/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91087228	ACATTACAGCGGTTT[A/G]TTATTCCTCAAACTC	66795
rs30295390	snp	G/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91086788	TGTGTCTGTGGCTTC[G/T]CTCGCTCCCAGCTTT	66795
rs30295391	snp	C/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91086182	GCTAAATTTGCTTCA[C/G]TGATAACCTAAGAAA	66795
rs30295392	snp	A/C	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91086083	AAGAATATTTGTAAC[A/C]CACCAAGTACTTTAT	66795
rs30295393	snp	A/C/T	0.244898	0.249948	intron-variant	Atg10	GRCm38.p3	13:91085892	GACACTGTAAAAACT[A/C/T]TACTTGATTAACCCC	66795
rs30295424	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91039788	AGGTTAGGAGTAATC[A/G]TATGGATGAATCTGC	66795
rs30295425	snp	G/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91039780	TGTTTTAAAGGTTAG[G/T]AGTAATCATATGGAT	66795
rs30295426	snp	A/T	0.396694	0.202437	intron-variant	Atg10	GRCm38.p3	13:91039748	CTCTAAATCAAATAT[A/T]ATTACAATAAAGCAA	66795
rs30295427	snp	G/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91039683	ATATATTCCCCAACT[G/T]TTAGTAGAGGGCACA	66795
rs30295428	snp	A/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91039525	CCGATCACATGAAAG[A/T]ACAGTTCTGAAGAAT	66795
rs30295429	snp	A/G	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91039494	GTCTCTGGTGATTAA[A/G]TGCTTACAGTGAATA	66795
rs30295430	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91039313	GCAGGAACAATCACT[A/G]TGCTGTGCTGTAAGG	66795
rs30295431	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91039221	GCTACTTGTGTATGT[A/G]TGTTTTAAGAACTAA	66795
rs30295432	snp	G/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91038978	ATGAACCATTTTCCA[G/T]TTTTCTCCACAAGAA	66795
rs30295433	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91038918	AGGCCCCTGAGTTTA[C/T]GTTAGGTAAAAGCAA	66795
rs30295434	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91127702	CCCACAAGTGCTTTC[A/G]GGTGTCCTTAGACAC	66795
rs30295435	snp	A/G	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91127672	GTGGGTAGCTCTCCT[A/G]AAAAGTCACCACTGC	66795
rs30295436	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91127435	GATGTGTGAGGAATG[C/T]CTGACCCTTTCTTTA	66795
rs30295437	snp	C/T	0.152778	0.230321	intron-variant	Atg10	GRCm38.p3	13:91127384	CACAGGCCACCAGGG[C/T]AGATTTGTGACTTCT	66795
rs30295438	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91126148	TATTCTATTGCTTTA[C/T]GACTGAGCAATTCTA	66795
rs30295439	snp	A/G	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91126066	CACATCATACTTAAT[A/G]TTAGAGTGTACTTAT	66795
rs30295440	snp	G/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91125846	TGAATACTATCACAG[G/T]GTCAATATTTCCCTT	66795
rs30295441	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91125669	AGGGTCCTTACTTAA[C/T]GAGTTTACAGGCTGA	66795
rs30295442	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91125532	AAGCAATTCAGAATG[A/G]AGTGCCACAGAGAGG	66795
rs30295443	snp	C/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91125516	ACAGCTTAGTCTAAA[C/G]AAGCAATTCAGAATG	66795
rs30295464	snp	A/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91007975	ACAGAATATATGTGT[A/T]CAGCAACCATTCTAT	66795
rs30295465	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91007940	AAGTAGAATGAAAAA[C/T]AAAGTTAAAGAAATG	66795
rs30295466	snp	A/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91007905	AAAATGTACTAGTGA[A/G]AAAAAGCTGAAGAGT	66795
rs30295467	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91007827	ATTTATGGGCCACTC[C/T]TTAAAACAATACATT	66795
rs30295468	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91007710	GTAGATTGAACAGAA[A/G]TAAGTACACCTGGAC	66795
rs30295469	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91007273	TATACCTACACAGTA[A/G]AGCACACTGTTATAG	66795
rs30295470	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91007206	AAAACCTTTAATGTA[C/T]ATCTGAAGGCTGAAT	66795
rs30295471	snp	G/T	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91007126	GAATATAAGGAAGCA[G/T]AGGTAACCATGATTA	66795
rs30295472	snp	A/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91007022	TCAGAGAAAGGATAG[A/T]TGCTCTTTGCTTTTC	66795
rs30295473	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91006875	TGGGATTTTAAATAA[C/T]TTAATTTTCTCCTAT	66795
rs30295634	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91142202	AATCAATCCTCATCG[C/T]AAAAATCTGCTTAAA	66795
rs30295635	snp	A/T	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91142168	TTATAGACCCCTTGA[A/T]TTCTTCTATCATGAG	66795
rs30295636	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91142115	CCCATTGAAAAAGTA[C/T]AGTTATAGCTAAATT	66795
rs30295637	snp	A/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91141919	TGTAGCCATTGGAGT[A/G]TCACAATTTTAGGGT	66795
rs30295638	snp	A/C	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91141876	TCTACAGGCACAATC[A/C]GCGACTATCAGCTGA	66795
rs30295639	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91141523	TCCTCATTTACATCA[C/T]GGTGTTTCCATCCAC	66795
rs30295640	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91141028	ATCAAGATTGTTGCA[A/G]TACTGACTCTGGGCC	66795
rs30295641	snp	A/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91140838	GGTCTGATATGAAGA[A/G]CTTAGATCAGATAAA	66795
rs30295642	snp	A/G	0.165289	0.235211	intron-variant	Atg10	Mm_Celera	13:91140135	TCAAAGGCCACCTAT[A/G]TGTTGGTCAATGTAT	66795
rs30295643	snp	A/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91139910	CCACTGATTTTTTTT[A/T]AACAGGGTCATATAT	66795
rs30295694	snp	C/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91107885	GAACTGTTTTTGATA[C/G]CATGGAAGGAAGCAG	66795
rs30295695	snp	A/C	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91107812	GTGTTCTCGCTGGGA[A/C]GATTAGTAATGCCGC	66795
rs30295696	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91107722	ATAAAAATATTCTGA[A/G]CCCAGACAGGCTGCA	66795
rs30295697	snp	C/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91107676	CTTAGAAATAGATGC[C/G]TGCGTGCACCTGCTT	66795
rs30295698	snp	G/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91107500	GCAAAAGGGAGAGGG[G/T]TCCATTTTGAGCCAA	66795
rs30295699	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91107382	AGCCACTCATCAATG[A/G]AATATAACAATAGAA	66795
rs30295700	snp	C/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91107304	CCCCTTATGAACTCT[C/G]AAGACTTCAATACTG	66795
rs30295701	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91107163	GTGTTAATAAAAGGC[A/G]TTGGTATACAGAACC	66795
rs30295702	snp	G/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91107083	ATTATTTGAACAAAT[G/T]ATTTTATAAACAAAA	66795
rs30295703	snp	A/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91105998	AAGATGGTAATTAAA[A/T]GATGTGATATTCAGC	66795
rs30295874	snp	G/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91060435	CTATAAATCAGAGAA[G/T]ACAGGAACAATATTC	66795
rs30295875	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91052273	TACAGAGCATCTCTG[C/T]GTTCCAAATCTAGAG	66795
rs30295876	snp	C/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91051647	GTATAGTAGCCTGGG[C/G]AAAACACTAAGTTTT	66795
rs30295877	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91049790	AGTGTGGTTGTTGCT[C/T]TTTCATATTATTATT	66795
rs30295878	snp	C/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:91049752	CTGCCATGTCTTAGG[C/T]ACTATGCTTATTCTG	66795
rs30295879	snp	A/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91049435	CTAGTTCTTTCCATA[A/T]ATGAGTAAACCTACA	66795
rs30295880	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91049394	CTTAGGCAAGTAGGA[C/T]TTCAGAAGTCATCAT	66795
rs30295881	snp	A/C	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91049347	AAAGTTTGGCTAGGG[A/C]CATTTTCTAAAGAAA	66795
rs30295882	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91049258	TGACCATCCAAGGAT[A/G]GGAAACTAAATTATC	66795
rs30295883	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91049194	TTATAAGCAGAAACT[A/C]ACAAAGGCCTGCATG	66795
rs30296144	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91085763	TGATCTCCTAGAGAC[C/T]TCAGAGCCTGGGGCA	66795
rs30296145	snp	C/G	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91084295	ACTAATCTAAATGCT[C/G]AATAATTGCACATAG	66795
rs30296146	snp	C/T	0.375	0.216506	intron-variant	Atg10	GRCm38.p3	13:91084291	TTGGACTAATCTAAA[C/T]GCTCAATAATTGCAC	66795
rs30296147	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91084262	GAACAGTATGAAAAA[C/T]GATCATTGTCACTTT	66795
rs30296148	snp	G/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91084216	CTCCTAAAATCCAAG[G/T]GAATTCAAAATATAG	66795
rs30296149	snp	C/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91084142	CACATGACTATGCTA[C/G]CAAAGTTCACGCATA	66795
rs30296150	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91084039	GTGCAGAGTCACTGG[A/C]AAATCTCCACAGTCA	66795
rs30296151	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91084010	AAAATAGTCAGTCAG[C/T]CAACAATTACTAAGT	66795
rs30296152	snp	G/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91082765	GGAACGCATGGAGAC[G/T]GAACCAAACTCCACA	66795
rs30296153	snp	C/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91082577	TCTGAAGCAGCAATC[C/T]TAAGGTTTTATAAAA	66795
rs30296294	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91006698	ATTTTTTAAATCCAG[A/G]ACCATAGTATGATTC	66795
rs30296295	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91006662	AATATTTAAACATTC[A/G]GATGAAAAGTCAATG	66795
rs30296296	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91006622	AAATAAAGAGACCAG[C/T]TTAGAATTCTGCGAG	66795
rs30296297	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91006574	TACTAAGGAGCTTGG[C/T]AATACAAATTGAAAA	66795
rs30296298	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91006227	CACCAACCTTATTAT[C/T]TAGAGAAGGCAGCTG	66795
rs30296299	snp	C/T	0.336735	0.234472	intron-variant	Atg10	Mm_Celera	13:91006142	AAGAATTCAAAATAA[C/T]GTTTGTTTGGAAAGG	66795
rs30296300	snp	A/G/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91006090	ACACCATACCTAGCT[A/G/T]GGAACAAGTTCTGAA	66795
rs30296301	snp	A/G	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91005744	TATTTGTCTCTTAGC[A/G]CATTGCTTCTGGGGT	66795
rs30296302	snp	A/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91005584	CTTCTCAAGGAAGTT[A/T]GTAACTCCATACTGG	66795
rs30296303	snp	C/T	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91005559	GAAAAGGGTCCAAAG[C/T]TTTTATCAGCTTCTC	66795
rs30296374	snp	G/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91038187	TACTGCAGTGTGTGA[G/T]GTGATGACATGGTCT	66795
rs30296375	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91038077	CCATAATCAATGCTT[C/T]TCACTTTGTAGGTAA	66795
rs30296376	snp	C/T	0.459184	0.136902	intron-variant	Atg10	GRCm38.p3	13:91037940	TGCTTAGAGAGTCTT[C/T]ACTATTGACTTATCC	66795
rs30296377	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91037783	GTCTCTGAGAAGCAA[C/T]GGATTCAATAGTAAA	66795
rs30296378	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91037523	GAAGCTTAGACAAAA[A/G]AGTGAGACCTTGTTT	66795
rs30296379	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91037449	TGGTTAGGCATGGTC[A/G]CGCCCACAACCATAA	66795
rs30296380	snp	C/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91037394	CCGAGAAGAACTCAC[C/T]TCTCTTCAGTCCGTG	66795
rs30296381	snp	A/G	0.132653	0.220748	intron-variant	Atg10	Mm_Celera	13:91037348	CCTGCCCAAACCAAC[A/G]AGGACAAAAGCAGTT	66795
rs30296382	snp	A/C	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91037288	CAAAGAAAAGGGCAG[A/C]GACCTCTCACTCAAA	66795
rs30296383	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91037163	TACAAGGTAGAAAAA[A/G]AGATGCACCAATATA	66795
rs30296464	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91125479	GAAAATGCTTACCAC[A/G]TCACACCAAAGAAAA	66795
rs30296465	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91125312	CTGTTGCACCAAGAC[C/T]TCCATCCCTCTAACA	66795
rs30296466	snp	C/T	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91125283	AAATCTCCCTGTTGC[C/T]ACAAGCCATGATCCT	66795
rs30296467	snp	A/C/T	0.297521	0.245442	intron-variant	Atg10	Mm_Celera	13:91125254	AAAAACATGTGCATA[A/C/T]CACTTAGGTTAGGAA	66795
rs30296468	snp	C/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91125066	TGCATACAGCGGTGT[C/T]GGAGCAACCAAATGA	66795
rs30296469	snp	A/T	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91124853	TAAAGCACCATGTAA[A/T]GATACCTAGGAAACG	66795
rs30296470	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91124829	AACTCCAGGCAGCGC[A/G]GAGAGCCATAAAGCA	66795
rs30296471	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91124745	TGAGAGCAGGTATCC[A/G]GCGTTGCCGAACTGC	66795
rs30296472	snp	A/G	0.152778	0.230321	intron-variant	Atg10	Mm_Celera	13:91124663	TCAATAAAGGAATTG[A/G]AAGAAAAGAATAAGA	66795
rs30296473	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:91124460	AAAAAAAGCAAAAAG[A/G]AAATATTACTAATAA	66795
rs30296594	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91105481	AAATTTCCCCAGTAA[A/G]GAGAGCCAGTATAAA	66795
rs30296595	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91105307	AAATTACTCCAAACA[C/T]AACTGAGTAGGCCGG	66795
rs30296596	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91103715	TTTGGCAAAAATGGT[A/G]ATTTTAAACTTTATT	66795
rs30296597	snp	A/G	0.260355	0.249785	intron-variant	Atg10	Mm_Celera	13:91102956	AACAGGGTTTACATA[A/G]TTGGAATAAAATGAA	66795
rs30296598	snp	A/G/T	0.244898	0.249948	intron-variant	Atg10	GRCm38.p3	13:91102574	ACCTTAAGAACATGC[A/G/T]AAATGTTTCATTCTT	66795
rs30296599	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91101622	CTAACTAGACTGTTA[C/T]GGATGAGCTAGAAGC	66795
rs30296600	snp	A/G	0.48	0.0979796	intron-variant	Atg10	Mm_Celera	13:91101603	CAAGTTTACTTTAAT[A/G]CTCCTAACTAGACTG	66795
rs30296601	snp	A/G	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91101174	ATGAAATATAAATAT[A/G]TGCAGTCAATTGCAA	66795
rs30296602	snp	C/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91100733	GCTTCAAAAGACTGA[C/T]TATACTGCTTTACAA	66795
rs30296603	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91100481	ATATGAGCTGACAAA[C/T]GGTGGAGGTGGACAG	66795
rs30296634	snp	A/G	0.375	0.216506	intron-variant	Atg10	Mm_Celera	13:90974020	TCCCAATTTCTAAGG[A/G]AAGTATTACAGAATT	66795
rs30296635	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:90973671	GAAAATCAGCGAAAC[C/T]ACCATGCTAGCATGC	66795
rs30296636	snp	A/T	0.277778	0.248452	intron-variant	Atg10	Mm_Celera	13:90973577	CCATTAGGGGACAGG[A/T]CTGTGTCTGCCAGGG	66795
rs30296637	snp	C/T	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:90973246	GAATAATGGTTTCTA[C/T]TCTATGGTTTAAGTA	66795
rs30296638	snp	C/T	0.444444	0.157135	intron-variant	Atg10	Mm_Celera	13:90973204	TAGGTGCACATTTAG[C/T]GTTTGTGAATAAGAA	66795
rs30296639	snp	A/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90971601	ATATTATATTCTGGT[A/T]GGAGACATGGCCTGT	66795
rs30296640	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90971137	TCCACCCCCGAAGCC[C/T]ATTTGAGTTGTTATT	66795
rs30296641	snp	C/G/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90971044	AACGACATGGCCTGA[C/G/T]TGTTATCTTGGCAAG	66795
rs30296642	snp	C/T	0.244898	0.249948	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90970787	GCGTCTGCTATCTCT[C/T]GTCTGCATCTATAAC	66795
rs30296643	snp	A/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Atg10, Gm35245	Mm_Celera	13:90970452	CTGCCTAGCGACTGA[A/T]AACACGGCCAATGTG	66795
rs30296684	snp	G/T	0.142012	0.225474	intron-variant	Atg10	Mm_Celera	13:91139092	CTCCACTAACAAGGA[G/T]TATGGTCCTAGGTCT	66795
rs30296685	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91138859	TTTCTCAAACCATGT[A/G]CCTAAACTCCACACC	66795
rs30296686	snp	G/T	0.244898	0.249948	intron-variant	Atg10	Mm_Celera	13:91138843	AACTTCATGCAATGT[G/T]TTTCTCAAACCATGT	66795
rs30296687	snp	A/G	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91138810	GAACATTTGCTGCCC[A/G]AAGATAAAGGTTATT	66795
rs30296688	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91138769	AACTGTTTGAAGTAA[A/G]GAGTTATATACACTG	66795
rs30296689	snp	C/G/T	0.124444	0.216185	intron-variant	Atg10	GRCm38.p3	13:91138439	ATTGATTTCCTATAT[C/G/T]GCACAAAGCAGATCT	66795
rs30296690	snp	A/T	0.124444	0.216185	intron-variant	Atg10	Mm_Celera	13:91138393	TTTTCTATAATCAAG[A/T]CAGGTGGGCCATGAT	66795
rs30296691	snp	C/T	0.124444	0.216185	intron-variant	Atg10	GRCm38.p3	13:91137965	AGCAGTGATTCTATG[C/T]CTCACCTCCACTGAC	66795
rs30296692	snp	A/G	0.231111	0.249285	intron-variant	Atg10	Mm_Celera	13:91137833	GATTGTCGTCCTTAG[A/G]ATATCCCCTTTTCTG	66795
rs30296693	snp	C/T	0.32	0.24	intron-variant	Atg10	Mm_Celera	13:91137820	AGAGGGCAGCTCTGA[C/T]TGTCGTCCTTAGGAT	66795

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