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

Hck

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6186603	snp	A/C/G	0.5	0	intron-variant	Hck	GRCm38.p3	2:153129722	GTGCTAGGTTCCCCC[A/C/G]CCCCTCATGCTCCTG	15162
rs6187150	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153129798	CCACAGCAGGCTGTA[A/G]AAGGTTCCTGTGCCN	15162
rs6187174	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153129813	NAAGGTTCCTGTGCC[A/G]GCTGATCCTCTTCTC	15162
rs6187679	snp	A/C	0.492188	0.0620098	synonymous-codon	Hck	Mm_Celera	2:153129866	GAGTGGTGGAAGGCA[A/C]GGTCCCTGGCTACCA	15162
rs6187791	snp	A/G	0.5	0	synonymous-codon	Hck	Mm_Celera	2:153129937	TAACTCTTTGGAGAC[A/G]GANGAGTAAGTGTTC	15162
rs6187792	snp	A/G	0.492188	0.0620098	synonymous-codon	Hck	Mm_Celera	2:153129940	CTCTTTGGAGACNGA[A/G]GAGTAAGTGTTCCAG	15162
rs6189176	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153130170	ATCCCACAGGCAAAA[A/G]GGGACGTTGCTTTTT	15162
rs6232131	snp	C/T	0.396694	0.202437	intron-variant	Hck	Mm_Celera	2:153144378	AGCAGATTCTGTGGG[C/T]TTCTAATATGTGAGG	15162
rs6232208	snp	A/G	0.46875	0.121031	synonymous-codon	Hck	Mm_Celera	2:153144427	GGTACAGATCTCAGA[A/G]GGCATGGCCTTCATT	15162
rs6232753	snp	A/G	0.459184	0.136902	synonymous-codon	Hck	Mm_Celera	2:153144538	CTTTGGACTGGCACG[A/G]ATCATCGAGGACAAT	15162
rs6233270	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153144632	ACTGACTCttgcatc[A/G]agtcaggaggcagac	15162
rs6329408	snp	A/G	0.396694	0.202437	intron-variant	Hck	Mm_Celera	2:153144288	AGGCAGAACAGTGCC[A/G]GTTGAGAGCCCAGGA	15162
rs13470389	snp	C/T			missense	Hck	Mm_Celera	2:153151100	ACATCCAGAGTGTGC[C/T]GGATGACTTCTACAC	15162
rs27352777	snp	A/C	0.456747	0.140554	utr-variant-3-prime	Hck	Mm_Celera	2:153151355	ATTTGCCTGGAATGA[A/C]TGAATTCAATCTATA	15162
rs27352778	snp	A/G	0.132653	0.220748	utr-variant-3-prime	Hck	Mm_Celera	2:153151200	TCAGTGCCTTGACAC[A/G]CCCAACTTGCTGGGC	15162
rs27352779	snp	G/T	0.48	0.0979796	utr-variant-3-prime	Hck	Mm_Celera	2:153151156	CAGCCTTGACGGCAG[G/T]AAGGACATGAGCAGA	15162
rs27352780	snp	G/T	0.497041	0.0383476	intron-variant	Hck	Mm_Celera	2:153150545	AACAACAGACCAAGA[G/T]ATGCAGAAACAGTAG	15162
rs27352781	snp	A/G	0.486111	0.0821678	intron-variant	Hck	Mm_Celera	2:153149292	TGCACTCAAGCAATC[A/G]AAGTTCAGCTATTTG	15162
rs27352782	snp	A/G	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153149278	TTCCCACACCTTACT[A/G]CACTCAAGCAATCGA	15162
rs27352783	snp	A/G	0.277778	0.248452	intron-variant	Hck	Mm_Celera	2:153149124	CTCCAGCCCAACCTG[A/G]CAATGGCCCATCTCG	15162
rs27352784	snp	A/G	0.345679	0.230967	intron-variant	Hck	Mm_Celera	2:153148850	CATTGCAAGGAAATC[A/G]CTATTTGTAGAGGGC	15162
rs27352785	snp	C/T	0.345679	0.230967	intron-variant	Hck	Mm_Celera	2:153148818	AAGACAAATGTCCCT[C/T]GGTAACATGGGTAAC	15162
rs27352786	snp	A/C	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153147982	AGTGTTCTGATGGTA[A/C]AGACATAGTTGCATT	15162
rs27352787	snp	A/T	0.46875	0.121031	intron-variant	Hck	Mm_Celera	2:153147946	AGCAGAGAGTGATTG[A/T]GAGCCTGGTCATTTA	15162
rs27352788	snp	C/T	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153147835	CCTTCTAGCTCCTTC[C/T]GCCCTACAGCCCTGC	15162
rs27352789	snp	C/G	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153147304	GTGCTCAGGCCTGCG[C/G]TGGGACTTTAACCAT	15162
rs27352790	snp	C/T	0.345679	0.230967	intron-variant	Hck	Mm_Celera	2:153147269	CTAGCATTTTCATCA[C/T]ACAAAGGGGCTAGCT	15162
rs27352791	snp	A/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153147255	GACACCTAAAAGCAC[A/T]AGCATTTTCATCATA	15162
rs27352792	snp	G/T	0.396694	0.202437	intron-variant	Hck	Mm_Celera	2:153147206	TCTTAACTTAGCGGT[G/T]GCTTGGTATATGGTT	15162
rs27352793	snp	C/T	0.152778	0.230321	intron-variant	Hck	Mm_Celera	2:153147158	CGGCCATAATACAAG[C/T]GTCGCCGAATTCCAA	15162
rs27352794	snp	A/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153147144	CTTAATCACTTACTC[A/G]GCCATAATACAAGCG	15162
rs27352795	snp	G/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153146348	CATAAAAGAGAAGTA[G/T]GACATAAAGAAAATG	15162
rs27352796	snp	G/T	0.277778	0.248452	intron-variant	Hck	Mm_Celera	2:153145843	GGTACTGCCTCAGAA[G/T]AGCTGGAAGGAGCCT	15162
rs27352797	snp	A/C	0.345679	0.230967	intron-variant	Hck	Mm_Celera	2:153145189	CAGAGTAGATGCCAG[A/C]AGGTTCTACATCATG	15162
rs27352798	snp	C/G	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153145084	CACTGACACAGAAGA[C/G]TATAGACTTCACCCC	15162
rs27352799	snp	C/T	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153144619	AGATCTGTCCTAGAC[C/T]GACTCTTGCATCAAG	15162
rs27352800	snp	C/T	0.42	0.183303	intron-variant	Hck	Mm_Celera	2:153143439	AGTCTGCCATTATCA[C/T]TCTTCATGCTCAGAG	15162
rs27352801	snp	C/T	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153143417	GCTACACTGAAGGGC[C/T]TCGTGAAGTCTGCCA	15162
rs27352802	snp	C/T	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153143347	CTTTCTTCCAGAAGC[C/T]TTAAGAATAAGAATC	15162
rs27352803	snp	C/T	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153143303	ATGGAGCTTTATCTT[C/T]CACCTCTTTTGTCCT	15162
rs27352804	snp	C/T	0.18	0.24	intron-variant	Hck	Mm_Celera	2:153143289	AGGCTTTCTGGGCAA[C/T]GGAGCTTTATCTTTC	15162
rs27352805	snp	A/G	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153143243	AGTCTGCCTTCACAG[A/G]GCTCCAAGGTAGTTC	15162
rs27352806	snp	A/G	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153143061	TTACTGGCCAGCTCT[A/G]TTTTAGGCTGTCTGA	15162
rs27352807	snp	A/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153142713	AGAGGTTGGTAAGAG[A/T]CACATGCTATGCAGC	15162
rs27352808	snp	A/G	0.277778	0.248452	intron-variant	Hck	Mm_Celera	2:153142694	GTGGGAAAGTACTAG[A/G]CACAGAGGTTGGTAA	15162
rs27352809	snp	C/T	0.35503	0.226867	intron-variant	Hck	Mm_Celera	2:153142468	GTGAATACTAGATGG[C/T]AGACACTGTCCTTGC	15162
rs27352810	snp	C/T	0.336735	0.234472	intron-variant	Hck	Mm_Celera	2:153142379	GCAGGGTGTTTGTAT[C/T]AGTCCCAGATCTGCC	15162
rs27352811	snp	A/G/T	0.375	0.216506	intron-variant	Hck	GRCm38.p3	2:153141093	GTGTTATCATTTCAG[A/G/T]ATACTAAGTCTTTAT	15162
rs27352812	snp	A/G	0.42	0.183303	intron-variant	Hck	Mm_Celera	2:153140005	ACGTTGTACAAAGCC[A/G]GCTAACATTCTTTCT	15162
rs27352813	snp	C/T	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153139945	CAAAAATGGTTCAGT[C/T]GTCCAGAGCTTTCCT	15162
rs27352814	snp	C/T	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153139740	TGACAATGGCAAACA[C/T]CACTGGCTTTATGCA	15162
rs27352815	snp	C/G	0.297521	0.245442	intron-variant	Hck	Mm_Celera	2:153139484	CTACAGACCTGAAAT[C/G]GAGGTATGAAGAATT	15162
rs27352816	snp	C/T	0.165289	0.235211	intron-variant	Hck	Mm_Celera	2:153139462	AGGTAATTGTCATTC[C/T]GTCGTCCTACAGACC	15162
rs27352817	snp	C/G	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153137835	ATAAATGCTGGGAGT[C/G]AAGACTAATCTACTA	15162
rs27352818	snp	A/G	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153137526	GTTAGTTTTAGAACA[A/G]CTGGTTTATAGTCAT	15162
rs27352819	snp	A/G	0.297521	0.245442	intron-variant	Hck	Mm_Celera	2:153137096	GCTTCCTTGTGACTC[A/G]TACCTGGGAACCTCA	15162
rs27352820	snp	A/T	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153136892	GGTGCGTGGGCAGGG[A/T]TAGAGTGTGGGCCAA	15162
rs27352821	snp	A/G	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153136562	CCAGAGAAGGTAGGT[A/G]TTTCAGTTGTACTCA	15162
rs27352822	snp	C/T	0.396694	0.202437	intron-variant	Hck	Mm_Celera	2:153136512	GCCCTTCAGTGAGAG[C/T]TTATCCCTTCCACTT	15162
rs27352823	snp	A/G	0.297521	0.245442	intron-variant	Hck	Mm_Celera	2:153136391	GTCATGGGCTGGCCC[A/G]GAGCCTCCAGTCCTC	15162
rs27352824	snp	A/G	0.197531	0.244432	intron-variant	Hck	Mm_Celera	2:153136163	TGGATGACAAGGACA[A/G]AAAAGTAGGTGTGAT	15162
rs27352825	snp	C/T	0.21875	0.248039	intron-variant	Hck	Mm_Celera	2:153136133	AGTTTGAGCATGTGT[C/T]GGAGGTGACCTTGGT	15162
rs27352826	snp	C/T	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153135696	GTTAATGTGTAAAAG[C/T]CAGAGTGAGGCCAGA	15162
rs27352827	snp	C/T	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135554	TCCTGGCATCCAAGA[C/T]ACACAGAGAAAGAAA	15162
rs27352828	snp	A/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135331	GATAAAGTGAGTTTT[A/G]AAAGCCTGTGGCTCA	15162
rs27352829	snp	C/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135287	CAGATGGAAAGGACG[C/G]AGCTTGTAGAGATGC	15162
rs27352830	snp	C/T	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135244	GGTCACAATACCTGA[C/T]CCACCATGTTAACAC	15162
rs27352831	snp	G/T	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153135204	TGGTCCTTGGCCCAG[G/T]ACCTTGAGAACAGGA	15162
rs27352832	snp	C/T	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153135044	GGCCTCTTGTGATGG[C/T]GAAAATTCATAGTGA	15162
rs27352833	snp	G/T	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153134878	ATAATAACCACAGGA[G/T]GCCACTCCTCAGATA	15162
rs27352834	snp	A/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153134551	GACATGAGGGTGGCG[A/G]TATACAGGTGTCATT	15162
rs27352835	snp	A/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153134471	GTGGCATGCAGCTCT[A/G]CACTCAGACTTCCTG	15162
rs27352836	snp	C/T	0.492188	0.0620098	intron-variant	Hck	Mm_Celera	2:153134331	ACAGCTTTTATTCCT[C/T]AGCACCTTGGCTTTG	15162
rs27352837	snp	A/G	0.49827	0.0293608	intron-variant	Hck	Mm_Celera	2:153134305	GCCAGGCTGTGAAGC[A/G]GTCACTAGCCACAGC	15162
rs27352838	snp	A/C	0.475309	0.108333	synonymous-codon	Hck	Mm_Celera	2:153134173	TTCTACATCTCTCCA[A/C]GGAGCACCTTCAGCA	15162
rs27352839	snp	G/T	0.475309	0.108333	intron-variant	Hck	Mm_Celera	2:153134024	GACATCAGGTAGCAG[G/T]CTTCTAAGGTGCCAT	15162
rs27352840	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153133496	CCTATTTTCACACTT[C/T]AGTAATCAGACCAGA	15162
rs27352841	snp	C/T	0.475309	0.108333	intron-variant	Hck	Mm_Celera	2:153133442	AGCTGCAGGTGTTCA[C/T]ATAAGAGCATCCTGG	15162
rs27352842	snp	A/G	0.475309	0.108333	intron-variant	Hck	Mm_Celera	2:153133385	CTCTGAGTTCCCTGG[A/G]ACACCCCTGGACACT	15162
rs27352843	snp	C/T	0.484429	0.0868505	intron-variant	Hck	Mm_Celera	2:153133056	ACTGCGGCCACAGAT[C/T]GGAATGCTTGTGTAT	15162
rs27352844	snp	A/G	0.408163	0.193609	intron-variant	Hck	Mm_Celera	2:153132793	AAGTGAGGCTGATAC[A/G]TCTATAAAGCATCTG	15162
rs27352845	snp	C/G	0.473373	0.11227	intron-variant	Hck	Mm_Celera	2:153132545	TGGACAGGAAGGTGG[C/G]CTGGACTCGCTTCCA	15162
rs27352846	snp	A/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132521	ACCAACAGCCCAGTG[A/G]CAGACCTGTGGACAG	15162
rs27352847	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132465	CTGTGCCTAGAGTAG[C/T]TTAGAGATTGACCTG	15162
rs27352848	snp	C/T	0.473373	0.11227	intron-variant	Hck	Mm_Celera	2:153132253	ATTCCACATGCACAG[C/T]GAGCCTTTGGCTCTT	15162
rs27352849	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132229	CACATGCTGTGTGCA[C/T]GATTTCAGATTCCAC	15162
rs27352850	snp	A/C	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132185	CCGACTGGCATTCCC[A/C]TGGGTGAGTTTCCCC	15162
rs27352851	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132022	TGGGTGACCAGAGTT[C/T]AAAAATAAAATAAAA	15162
rs27352852	snp	A/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153132001	TTGGCAAAGAGTCAT[A/G]TGGAATGGGTGACCA	15162
rs27352853	snp	C/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153131593	TCCCCACTAGATCCT[C/G]GTCTGTTTTAAATAG	15162
rs27352854	snp	A/G	0.35503	0.226867	intron-variant	Hck	Mm_Celera	2:153131490	GGGCCTGGACTAGGT[A/G]GCTTCTTCTAGTTCT	15162
rs27352855	snp	A/G	0.473373	0.11227	intron-variant	Hck	Mm_Celera	2:153131372	GCAAGGCGCCTCTCC[A/G]ACCTTAGGGAAGTCC	15162
rs27352856	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153131193	GTCCATCCTGAGTCT[C/T]ACACTGTCCCTCATT	15162
rs27352857	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153130970	CTTGTGAGGATGAAA[A/G]GAACTTCAGCCACTA	15162
rs27352858	snp	C/G	0.456747	0.140554	intron-variant	Hck	Mm_Celera	2:153130939	CCCCATTGTGGTACA[C/G]AGACTGCTCCTTATT	15162
rs27352859	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153130892	AACAAAAGTCACCTG[A/G]CAGGCATGCTGATAT	15162
rs27352860	snp	G/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153130856	TCCCTTATTGATAAC[G/T]GAGGCAGCAGAGACC	15162
rs27352861	snp	A/G	0.408163	0.193609	intron-variant	Hck	Mm_Celera	2:153130125	CTCTGTGACTCTCTC[A/G]GAGAGGTGTTTTTAC	15162
rs27352862	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153129288	ATAGGACCTACCTCT[C/T]AGTAACAAAACCAGA	15162
rs27352863	snp	G/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153129033	ATCCTGGCATCTCCC[G/T]TCTTGGCAGGCTCTG	15162
rs27352864	snp	C/T	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153128849	AAACTAACCAGCACC[C/T]TTGTATAGTCTCTAA	15162
rs27352865	snp	C/T	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153128432	CAAAAAACCTCTGTA[C/T]TTGGCTTTTGTGAAG	15162
rs27352866	snp	A/C	0.5	0	intron-variant	Hck	Mm_Celera	2:153128216	CCTTTTCAACACAGG[A/C]TCCTCACAATTTCAG	15162
rs27352867	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153128077	AGTATTTCAAGGCAA[A/G]GGTCCCGATCACATT	15162
rs27352868	snp	A/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153127909	GAGACCTGTGGTTCT[A/G]ATGGCAGTGTCCCTT	15162
rs27352869	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153127690	CTTTATATAGACATA[A/G]TGAGTTGTGTGAATG	15162
rs27352870	snp	C/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153127468	AAAACAAGCATCCCT[C/G]CGTGCTTCCTCAAAT	15162
rs27352871	snp	A/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153127333	CTGTAAGTTAAGAAA[A/G]TATGTCTCAGGAGAA	15162
rs27352872	snp	C/T	0.46281	0.131194	intron-variant	Hck	Mm_Celera	2:153127298	TTATTCCCTCCTGTG[C/T]GGTGCTCGCCCAGAG	15162
rs27352873	snp	C/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153127290	TTGTCGAGTTATTCC[C/G]TCCTGTGTGGTGCTC	15162
rs27352874	snp	G/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153127242	CCCTGGGTCTTCTCC[G/T]GCCTGATTCTGAGGA	15162
rs27352875	snp	A/C	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153126340	GTGAGGAGATCAGGC[A/C]GCTGAGAAGCCATCG	15162
rs27352876	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153126300	CTGCTTGCCATCAGG[A/G]TTCAAAGAATCTTGG	15162
rs27352877	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153126208	TAGTATTGTCTCCAG[A/G]CTCCCACTCTGTCCT	15162
rs27352878	snp	C/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153126032	TAAAAGTGAGAGTTG[C/T]TGAGGCAGAGGTGAA	15162
rs27352879	snp	C/T	0.426035	0.177515	intron-variant	Hck	Mm_Celera	2:153124373	ACAAGCCACCTACCT[C/T]TAGGATGCTTTCCCC	15162
rs27352880	snp	A/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153124319	AGGGAGCTGCCACAG[A/G]GACTTTAAACCCTTT	15162
rs27352881	snp	A/G	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153124296	CAAGCTGGTGAGTAC[A/G]GCATCCCAGGGAGCT	15162
rs27352882	snp	G/T	0.459184	0.136902	synonymous-codon	Hck	Mm_Celera	2:153124272	TGTGCCGGATCCCAC[G/T]TCCTCCAGCAAGCTG	15162
rs27352883	snp	C/T	0.132653	0.220748	intron-variant	Hck	Mm_Celera	2:153124073	CTGAGGACCCAAGTA[C/T]TTTCACTCAAGGCTG	15162
rs27352884	snp	G/T	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153124005	TACCCTGCTGGTCCT[G/T]GGATTCCATGTGTGC	15162
rs27352885	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153123900	TCAGCTGTTTCCTGA[C/T]CCAAGGCCAACAGCA	15162
rs27352886	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153123773	GTGCTGGGGTGCCAT[C/T]CAGAGGCTGTGCTGA	15162
rs27352887	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153123672	ATGCCCAGTTATTAT[C/T]CTGGATTATTGGAGC	15162
rs27352888	snp	C/T	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153123536	TGTCAGCTAGCAATG[C/T]AACTTGAATGAACAA	15162
rs27352889	snp	A/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153123371	CTGTCACCCGTGGCT[A/G]GACAATCACAGCAAT	15162
rs27352890	snp	A/C	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153123121	GCCCTTAGCTCCCCA[A/C]AGTTAAGTTTTGACT	15162
rs27352891	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153123053	CCAGCCGAGTCTGGG[C/T]CTCAGTTCCAGGATC	15162
rs27352892	snp	A/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153122956	GCAGGCCACTTTCTC[A/G]GCAAACATATGGGCC	15162
rs27352893	snp	C/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153122945	TAGAGTAGCTTGCAG[C/G]CCACTTTCTCAGCAA	15162
rs27352894	snp	A/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153122767	GCTCTAACAACTTAA[A/G]TATAACTGAGCTTTC	15162
rs27352895	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153122542	GTAAACACACACAGG[C/T]GCTGCTTAATTTTCT	15162
rs27352896	snp	C/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153122413	TCTCTGCTGCATGCT[C/T]ACAGCTGCATCTGTC	15162
rs27352897	snp	A/G	0.35503	0.226867	intron-variant	Hck	Mm_Celera	2:153122348	TGAATATGTAAATCA[A/G]CCATGTAATGATGCT	15162
rs27352898	snp	A/G	0.391111	0.206368	intron-variant	Hck	Mm_Celera	2:153122318	TCCTGAGAGGGGTCC[A/G]GAGTTGGGTCTTCAT	15162
rs27352899	snp	A/G	0.489796	0.070696	intron-variant	Hck	Mm_Celera	2:153122155	GACAACCCCCAGCCC[A/G]TGAGACAAAGCACCC	15162
rs27352900	snp	A/G	0.426035	0.177515	intron-variant	Hck	Mm_Celera	2:153121795	AAGGTCAGCAGACAC[A/G]GTTGTCCTCTGAAAC	15162
rs27352901	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153121061	AAAGCCATATGTGGT[C/T]TGTTTAGGTGACCAG	15162
rs27352902	snp	A/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153121000	GTGGCTTTGAGATGT[A/G]ATTCTGTGTGTTTGA	15162
rs27352903	snp	A/C	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153120981	CAATGGAGTCTCTCT[A/C]TGTGTGGCTTTGAGA	15162
rs27352904	snp	A/G	0.459184	0.136902	intron-variant	Hck	Mm_Celera	2:153119836	TGAATGAGCTTGTGT[A/G]AGATTAAAAGGTTCT	15162
rs27352905	snp	C/T	0.426035	0.177515	intron-variant	Hck	Mm_Celera	2:153119774	AAGACTCGAACCTGC[C/T]GCGAAAAGCACAGGC	15162
rs27352906	snp	A/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153119748	GTACAAAACCAACTC[A/G]GCCTTCATGTAAGAC	15162
rs27352907	snp	A/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153119733	CATGCATCTCACTCT[A/G]TACAAAACCAACTCG	15162
rs27352908	snp	C/T	0.391111	0.206368	intron-variant	Hck	Mm_Celera	2:153117630	CATACCCAGCCATAT[C/T]CCTGACAAATATAGT	15162
rs27352909	snp	G/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153117573	AGAGAAGAGACCTAA[G/T]CTTAAAGTACAAAGC	15162
rs27352910	snp	G/T	0.408163	0.193609	intron-variant	Hck	Mm_Celera	2:153117361	ACCACAGCCTTTGTC[G/T]CCGAAGACCTCAAGC	15162
rs27352911	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153117286	GGCTACTTCTGCTCC[C/T]GGTGCCTGACTGGGA	15162
rs27352912	snp	C/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153117190	CATGTAGTAACTATA[C/G]AACTGAGGAGTCATA	15162
rs27352913	snp	A/C	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153117184	CTCTTCCATGTAGTA[A/C]CTATAGAACTGAGGA	15162
rs27352914	snp	G/T	0.426035	0.177515	intron-variant	Hck	Mm_Celera	2:153117148	CCTGGGAAACAGCCA[G/T]CCAGGCTAACTGGCT	15162
rs27352915	snp	A/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153116564	CAGAACTGAGTTGCA[A/G]CCTACTTGGCTTCTT	15162
rs27352916	snp	A/G	0.391111	0.206368	intron-variant	Hck	Mm_Celera	2:153116526	CTTTCCTAGACAGAG[A/G]CCACGGACTGATGCT	15162
rs27352917	snp	A/G	0.124444	0.216185	intron-variant	Hck	Mm_Celera	2:153116255	TTCTCTTGTACCAAG[A/G]CCTGCTCTCAGAGAA	15162
rs27352918	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153116250	TTAACTTCTCTTGTA[C/T]CAAGGCCTGCTCTCA	15162
rs27352919	snp	A/G	0.124444	0.216185	intron-variant	Hck	Mm_Celera	2:153116198	TTGACAAGATCCACA[A/G]TCCCCATCCTCACCC	15162
rs27352920	snp	C/T	0.408163	0.193609	intron-variant	Hck	Mm_Celera	2:153116183	TTCAGTGCCACCAGC[C/T]TGACAAGATCCACAG	15162
rs27352921	snp	A/G	0.124444	0.216185	intron-variant	Hck	Mm_Celera	2:153116104	AAGAGAACACAATAT[A/G]CTCACACCTCAGACC	15162
rs27352922	snp	A/G	0.124444	0.216185	intron-variant	Hck	Mm_Celera	2:153116063	GAAGAATGGGTTCCT[A/G]ATTCTGGTTTAGATC	15162
rs27352923	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153115821	ACCCCAAAAACTGCT[C/T]TAGAAAGGAACTTCT	15162
rs27352924	snp	A/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153115764	TACAGAGTAAGCATG[A/G]TTCTCTCAGAAAGAC	15162
rs27352925	snp	C/T	0.456747	0.140554	intron-variant	Hck	Mm_Celera	2:153115702	TTGGCCAGAGGAAGC[C/T]AAGTCTCCCAAAGGA	15162
rs27352926	snp	A/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153115566	GCCAAAGTCTCCAGA[A/T]GGCGGGGCCCCTTGC	15162
rs27352927	snp	C/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153114973	GCAAACTGGACCATC[C/G]TCCCCACCCAGACAC	15162
rs27352928	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153114935	CCAGCCAAGAAGCAC[C/T]TGGTTTTGTTGAGGA	15162
rs27352929	snp	A/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153114923	GGACAGTCAGCTCCA[A/G]CCAAGAAGCACTTGG	15162
rs27352930	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153114821	GGCATCTATGAGACA[C/T]GGTTGGGGTGTCTGA	15162
rs27352931	snp	A/G	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153114802	TCTAGTGTCTTTGAG[A/G]CTTGGCATCTATGAG	15162
rs27352932	snp	C/T	0.231111	0.249285	intron-variant	Hck	Mm_Celera	2:153113832	CAAGCATGTGCACTC[C/T]GTAGGATGAAAGTAC	15162
rs27352933	snp	A/G	0.455	0.143091	intron-variant	Hck	Mm_Celera	2:153113536	GGGAGGAGGCCCTTG[A/G]AGGGAGTGAAAGGAG	15162
rs27352934	snp	C/T	0.455	0.143091	intron-variant	Hck	Mm_Celera	2:153113463	CAGCACCTGCTTCCA[C/T]ATACACGTCAATAAG	15162
rs27352935	snp	C/G/T	0.32	0.24	intron-variant	Hck	GRCm38.p3	2:153112689	CTCTAGCTGTTGTGG[C/G/T]GGGAGCCGTCACCTC	15162
rs27352936	snp	A/C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153111960	TTTAATGAGAAGAGT[A/C/T]TTGAGACTTGGAAAG	15162
rs27352937	snp	C/T	0.401235	0.199068	intron-variant	Hck	Mm_Celera	2:153111882	TGGGCACAGGTACAG[C/T]TGTTTCTTGAGGAAA	15162
rs27352938	snp	A/T	0.432133	0.171253	intron-variant	Hck	Mm_Celera	2:153111617	ACTACTCTACACCAG[A/T]ACTGATTTATGAGGC	15162
rs27352939	snp	A/C/T	0.124444	0.216185	intron-variant	Hck	GRCm38.p3	2:153111588	ACTGCAACCTCTGAG[A/C/T]GGACTGTATGGGAAC	15162
rs27352940	snp	A/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153111221	AGGGATGTATCCTGA[A/G]ATCCTGGCAGATGCC	15162
rs27352941	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153110537	CTTTCCACTGTTCCC[A/G]TCCAGCCCGAGAGAT	15162
rs27352942	snp	C/T	0.465374	0.126941	intron-variant	Hck	Mm_Celera	2:153110094	TCAGGTGTGGACTTT[C/T]CCACTTGGACCATCC	15162
rs27352943	snp	C/T	0.48	0.0979796	intron-variant	Hck	Mm_Celera	2:153109984	GCTATCTTCCTGGCC[C/T]GAGATTTTCACACAT	15162
rs27352944	snp	A/C	0.455	0.143091	intron-variant	Hck	Mm_Celera	2:153109614	GGGGTTTAGGATTTC[A/C]GAGTGTGGCAGAATT	15162
rs27352945	snp	G/T	0.42	0.183303	intron-variant	Hck	Mm_Celera	2:153109601	ACACCTGATCAGAGG[G/T]GTTTAGGATTTCCGA	15162
rs27352946	snp	C/T	0.455	0.143091	intron-variant	Hck	Mm_Celera	2:153109448	GCTGTTTTACATTCA[C/T]CTGAAGCTGAGTTGT	15162
rs27352947	snp	A/G	0.255	0.24995	intron-variant	Hck	Mm_Celera	2:153109246	CACCCAGGCCTGGCT[A/G]TAGGTGTATATCTGA	15162
rs27352948	snp	A/C	0.124444	0.216185	intron-variant	Hck	Mm_Celera	2:153108963	GGTGAGGCGAATTGC[A/C]GCCACCCAGGGCGAC	15162
rs27352949	snp	A/T	0.465374	0.126941	intron-variant	Hck	Mm_Celera	2:153108914	GGCGGTGGGATGCGC[A/T]GTCTACGAAAGGTGG	15162
rs27352950	snp	C/G	0.124444	0.216185	intron-variant	Hck	Mm_Celera	2:153108891	CGTCCTAGGAGCAAC[C/G]GATCCCCGGCGGTGG	15162
rs27352951	snp	A/G	0.142012	0.225474	intron-variant	Hck	Mm_Celera	2:153108826	AGACCTCGGGCTCCA[A/G]GGATCTGAGATCCTG	15162
rs27352952	snp	A/C	0.444444	0.157135	upstream-variant-2KB	Hck	Mm_Celera	2:153108313	CCTTGGTGTCTGAGT[A/C]AGTCCTTCAAGGACT	15162
rs27352953	snp	A/C	0.35503	0.226867	upstream-variant-2KB	Hck	Mm_Celera	2:153108256	GGGCTTAAACGCACT[A/C]GTGGGGGAGGGGGAC	15162
rs27352954	snp	A/C	0.444444	0.157135	upstream-variant-2KB	Hck	Mm_Celera	2:153108222	TAGAATCCTTTGGAC[A/C]GGCTCATTACATCAT	15162
rs27352955	snp	A/C	0.124444	0.216185	upstream-variant-2KB	Hck	Mm_Celera	2:153107780	ACAAACTACGGAGAG[A/C]GAGGCCCTGGATTCC	15162
rs27352956	snp	A/G	0.48	0.0979796	upstream-variant-2KB	Hck	Mm_Celera	2:153107687	TCTTTGAAAGGAAGG[A/G]TAGGATCGGTTGATT	15162
rs27352957	snp	C/T	0.244898	0.249948	upstream-variant-2KB	Hck	Mm_Celera	2:153107618	AGAGGTTAGACTTAT[C/T]AGGGCGTGGTTAGAC	15162
rs27352958	snp	A/C	0.231111	0.249285	upstream-variant-2KB	Hck	Mm_Celera	2:153107603	CAGAATCCTAGAGGG[A/C]GAGGTTAGACTTATC	15162
rs27352959	snp	C/T	0.459184	0.136902	upstream-variant-2KB	Hck	Mm_Celera	2:153107293	GGGAGGACTCCTGTA[C/T]GTTTCTGCAGGTGTG	15162
rs27352960	snp	A/G	0.32	0.24	upstream-variant-2KB	Hck	Mm_Celera	2:153107237	CATGCACGCGTAAGC[A/G]AATGAATGAGAGATA	15162
rs27352961	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Hck	Mm_Celera	2:153107209	AAACATAGTACTGCT[A/G]AACGCATGCCTACAT	15162
rs27352962	snp	A/G	0.489796	0.070696	upstream-variant-2KB	Hck	Mm_Celera	2:153107057	AGCAAACACATTAGT[A/G]TTGGGTGACTGGGAT	15162
rs27352963	snp	A/T	0.18	0.24	upstream-variant-2KB	Hck	Mm_Celera	2:153107025	TAGAAATAGGGCATG[A/T]ATATATTAAAATACA	15162
rs27352964	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Hck	Mm_Celera	2:153107000	ACCTGTTCAAGACTC[A/G]GTCTATTTTTAGAAA	15162
rs27352965	snp	A/C	0.391111	0.206368	upstream-variant-2KB	Hck	Mm_Celera	2:153106878	GCTAGCTCTGTGACG[A/C]TGCCTTTATTGGCTT	15162
rs27352966	snp	C/T	0.497778	0.0332592	upstream-variant-2KB	Hck	Mm_Celera	2:153106829	GGGTGACAATGTGTG[C/T]GTATAATACACTGCC	15162
rs27352967	snp	A/G	0.124444	0.216185	upstream-variant-2KB	Hck	Mm_Celera	2:153106779	AGGCCTTTGTCTCTA[A/G]GTGGATAATCGGGGA	15162
rs27373668	snp	A/G	0.489796	0.070696	upstream-variant-2KB	Hck	Mm_Celera	2:153106722	GGCCTAAGGCCCTCC[A/G]GGCATCCCTCACCAA	15162
rs27373669	snp	A/G	0.48	0.0979796	upstream-variant-2KB	Hck	Mm_Celera	2:153106693	GCATGGTTGGGGCAG[A/G]CCAGAGTGCTGGAGG	15162
rs29527142	snp	C/G/T	0.444444	0.157135	intron-variant	Hck	GRCm38.p3	2:153141141	ATGACTTACATGGAT[C/G/T]GTGACGTAGCTCAAA	15162
rs29621200	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153134429	CCACGAGCCCCCACT[A/G]GGAGGGGCCTGTCTC	15162
rs29716889	snp	C/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153111369	CAAGCATTGCCTGAA[C/T]ACATGCATAGAAACT	15162
rs29719143	snp	A/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153133117	ATTACTGTAAGCTGG[A/G]CAGTTTAGAGCCACA	15162
rs29769080	snp	A/G	0.375	0.216506	utr-variant-5-prime	Hck	Mm_Celera	2:153108665	TTGCTCCGGGCTCTG[A/G]AGTCCGGGGCCACCA	15162
rs29813479	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153141358	TCTAGAGAATCTGGC[A/G]TCATATGAAGAACAG	15162
rs29818510	snp	C/G	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153111014	TCCAGTCTGTGTCTC[C/G]ATAAACAAATGTGTC	15162
rs29819765	snp	G/T	0.444444	0.157135	downstream-variant-500B	Hck	Mm_Celera	2:153151581	GTCAGTTAGATGCTT[G/T]TCCTGTAAGTCCAGG	15162
rs29913856	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153145646	TCTGCAGGGTGAGTT[C/T]CAGGACAGCCTGGAC	15162
rs29966441	snp	G/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153126661	ATATTAAGTAAGTAA[G/T]CAAATAAGCTCTTCC	15162
rs30576219	snp	C/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153117520	CACTGGCTGTGAGAA[C/G]GGTGTTCTCAGTGTT	15162
rs32911087	snp	A/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153145580	TGAAAGTCGTCAGGA[A/G]CTGTGGTGGCTGCGC	15162
rs32942834	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153126547	CAGAGGTTAAGAGCA[C/T]TGACTGCTCTTTCAG	15162
rs32958690	snp	C/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153142420	TGAGCAAGGCGCTTG[C/G]CTGCTCTGATGACAT	15162
rs32961412	snp	A/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153126531	GTCTGGAGAGATGGC[A/T]CAGAGGTTAAGAGCA	15162
rs32985692	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153112255	CTGTTAGTATTTCCC[C/T]GTGTCATTAAGATTG	15162
rs33031697	snp	A/C	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153110283	AGTTCTCACCGATCG[A/C]TCACAACAACAGAAA	15162
rs33048301	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153141163	TAGCTCAAATGTAGA[C/T]TCCTTCTTTGGCATG	15162
rs33099611	snp	C/T	0.5	0	intron-variant	Hck	Mm_Celera	2:153110388	GCACACATGTGATCT[C/T]TCTCTCTCTCTCTCT	15162
rs33112493	snp	A/G	0.444444	0.157135	downstream-variant-500B	Hck	Mm_Celera	2:153151501	TGGCGTATCAGATGG[A/G]GAATGACCTTCCCAG	15162
rs33125421	snp	A/G	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153109418	TGGATTCCAGCTTCC[A/G]ACTCTGTAAAATGGG	15162
rs33134390	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153140448	CTCAGATCCCGGGGA[A/G]GTCTAAGCAGAGGCT	15162
rs33183004	snp	C/T	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153113398	AGGTGGAAGTCCAGC[C/T]GGAATGTTCCAAGAT	15162
rs33253030	snp	G/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153109481	AGAGAAGGGGAGCAG[G/T]GCTGCTGGGTACTGG	15162
rs33257672	snp	A/G	0.5	0	utr-variant-3-prime	Hck	Mm_Celera	2:153151151	AGCAGCAGCCTTGAC[A/G]GCAGGAAGGACATGA	15162
rs33274696	snp	C/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153126727	GCATTGCAAGCTTAA[C/T]TGCCTGAGTTAAGAC	15162
rs33339129	snp	G/T	0.5	0	downstream-variant-500B	Hck	Mm_Celera	2:153151711	AGTCTGGCCTAATTG[G/T]CGAGGGCCAAGTCAA	15162
rs33392280	snp	G/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153108801	CACACCCCCGTCCCC[G/T]AGAACGTGCAGACCT	15162
rs33394045	snp	A/G	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153112665	GGTGGAGCAGGCATG[A/G]GGGCAAGGCTCTAGC	15162
rs33397577	snp	C/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153140726	AGCAACCACATGGTG[C/G]CTCACAACCACCTGT	15162
rs33428842	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153141383	GAACAGTCTGTATCC[A/G]TGGGTTCTGCATCTG	15162
rs33481711	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153141019	AATATGGCTTAGTCA[A/G]TAGTGTGCTTGCCCA	15162
rs33486501	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153131061	TAGCTCTTTCCCACT[A/G]ACCCACCCCCTAAAA	15162
rs33498828	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153112394	ATAAGTGTCTGTCTA[C/T]ACATATGTGTGTGCC	15162
rs33505278	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153142717	GTTGGTAAGAGACAC[A/G]TGCTATGCAGCTATG	15162
rs33510921	snp	C/T	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153126662	TATTAAGTAAGTAAG[C/T]AAATAAGCTCTTCCT	15162
rs33522873	snp	A/G	0.444444	0.157135	intron-variant	Hck	Mm_Celera	2:153110623	ACCAAAGGGAGGCCT[A/G]GGGAAAGATACTGAG	15162
rs33533851	snp	A/T	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153111203	ATAAAACTTCAGTCA[A/T]CAAGGGATGTATCCT	15162
rs33551964	snp	C/G/T	0.375	0.216506	intron-variant	Hck	Mm_Celera	2:153110865	ACTAATGTCAGTGTG[C/G/T]GGGCATGTTTGCTTC	15162
rs33554000	snp	A/G	0.5	0	downstream-variant-500B	Hck	Mm_Celera	2:153151636	ATGTAAGAATGCTGG[A/G]TGTGCTGGTGTGCAT	15162
rs33686384	snp	A/G	0.32	0.24	intron-variant	Hck	Mm_Celera	2:153113347	GACAGAGCAGATACA[A/G]AGAGATCTCCATGGC	15162
rs33713022	snp	A/G	0.444444	0.157135	downstream-variant-500B	Hck	Mm_Celera	2:153151490	TTTCTGCTGTGTGGC[A/G]TATCAGATGGGGAAT	15162
rs33723877	snp	A/G	0.5	0	intron-variant	Hck	Mm_Celera	2:153140821	TAAATGAAGCTTTGG[A/G]CCAGAGCAAGCAGGG	15162
rs45654343	snp	C/T			intron-variant	Hck	Mm_Celera	2:153117929	GGGACAGAAATCACA[C/T]GATCATCTCAATGGA	15162
rs45688582	snp	A/C			intron-variant	Hck	Mm_Celera	2:153137478	TGTGTGTCTCCACAC[A/C]CGGCTTCTCAGAGTT	15162
rs45740556	snp	G/T			intron-variant	Hck	Mm_Celera	2:153119825	TCCAAGAGTTATGAA[G/T]GAGCTTGTGTAAGAT	15162
rs45743045	snp	C/T			downstream-variant-500B	Hck	Mm_Celera	2:153151757	AAAGGAGATGGCTGG[C/T]ACTCTGGAGAATGAC	15162
rs45771968	snp	C/T			intron-variant	Hck	Mm_Celera	2:153125139	CCCAATGGCATGCTT[C/T]CTTAGCAAGGCCACA	15162
rs45784664	snp	C/T			intron-variant	Hck	Mm_Celera	2:153137316	CTTTGGGCCACTGTA[C/T]CCTGGGATTATTCAG	15162
rs45786506	snp	C/T			intron-variant	Hck	Mm_Celera	2:153116567	AACTGAGTTGCAACC[C/T]ACTTGGCTTCTTTGG	15162
rs45801455	snp	A/T			intron-variant	Hck	Mm_Celera	2:153124933	ATGCCAGGACCAGGG[A/T]AGCTTGTAGAAGAAG	15162
rs45814648	snp	A/G			intron-variant	Hck	Mm_Celera	2:153132425	GTGAGCATTTAGGCT[A/G]CAGGGAGGCCCAGCT	15162
rs45823219	snp	A/G			downstream-variant-500B	Hck	Mm_Celera	2:153151507	ATCAGATGGAGAATG[A/G]CCTTCCCAGAGGCCA	15162
rs45846398	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120487	GAATGGATAAAGAAA[A/G]TGAGATACATATACA	15162
rs45852150	snp	A/C			intron-variant	Hck	Mm_Celera	2:153141267	TCAGTGGTTAAGAGC[A/C]CTGGCTGCTCTTCCA	15162
rs45861184	snp	A/G			intron-variant	Hck	Mm_Celera	2:153136260	ATGCTATGCAGGCTC[A/G]TGTTGCAGTCTAACT	15162
rs45903375	snp	A/G			intron-variant	Hck	Mm_Celera	2:153119646	AGTTTCTTTGTGCAA[A/G]GCATGATGGTTAATG	15162
rs45911061	snp	C/T			intron-variant	Hck	Mm_Celera	2:153135641	AGTGTGTGGCAAGTC[C/T]CTGCAGCTGAGGACT	15162
rs45920902	snp	C/T			intron-variant	Hck	Mm_Celera	2:153116735	CTCCAGAAGAGGGCG[C/T]CGGATCTTGTTACAG	15162
rs45965879	snp	C/T			intron-variant	Hck	Mm_Celera	2:153143670	CCCAGGCAGTTTCCA[C/T]GACCATCCAATGGAA	15162
rs46002866	snp	A/G			intron-variant	Hck	Mm_Celera	2:153145379	AGACAACTGTTGGAA[A/G]CCCTGGGAGCATGCT	15162
rs46063608	snp	A/C			intron-variant	Hck	Mm_Celera	2:153118946	CCTGAGACAATGCTA[A/C]GTTACCAAAAGCAAT	15162
rs46130969	snp	A/C			intron-variant	Hck	Mm_Celera	2:153118980	CAGTTTCAGTATAAT[A/C]CCCATAAAAACCCCA	15162
rs46133882	snp	C/G			intron-variant	Hck	Mm_Celera	2:153124978	TCACGGGTCCAGAGG[C/G]TTAGAGTCCATGATG	15162
rs46216615	snp	A/C			intron-variant	Hck	Mm_Celera	2:153127774	CACGGGAATCCTGCT[A/C]GGTTCCCAGTGCTGG	15162
rs46242284	snp	C/G			intron-variant	Hck	GRCm38.p3	2:153149911	GGTAGCACATGGGCA[C/G]CTGGGGCAGGTGGTG	15162
rs46276803	snp	A/G			intron-variant	Hck	Mm_Celera	2:153124935	GCCAGGACCAGGGTA[A/G]CTTGTAGAAGAAGGA	15162
rs46285415	snp	A/G			intron-variant	Hck	Mm_Celera	2:153144918	AGGTGAGAGGTGAGA[A/G]TAATGCTATGCCCAG	15162
rs46318636	snp	C/G			intron-variant	Hck	Mm_Celera	2:153114736	AGAACCCAGGGCTCT[C/G]TTTGTGCAAGCTGAA	15162
rs46323232	snp	A/T			intron-variant	Hck	Mm_Celera	2:153114480	CCGAAGGTTCTGGGG[A/T]TTAAACTCTGATCCT	15162
rs46325737	snp	A/C			intron-variant	Hck	Mm_Celera	2:153137255	CCTGCTATGACCAAC[A/C]CACAGAATCATGACA	15162
rs46350635	snp	G/T			intron-variant	Hck	Mm_Celera	2:153138927	TGTGAGCCACCATGT[G/T]GGTGCTAGGACTGAA	15162
rs46405469	snp	C/T			intron-variant	Hck	Mm_Celera	2:153116701	TTATATGTAAGTACA[C/T]TGTAGCTGTCTTCAG	15162
rs46424045	snp	C/T			intron-variant	Hck	Mm_Celera	2:153137420	GGCTAGCCTCAATCT[C/T]GTAGCTGTCCTGCCT	15162
rs46425937	snp	A/C			intron-variant	Hck	Mm_Celera	2:153146892	AACTTCTCATCTCTG[A/C]TGGGATTTTGTCCAG	15162
rs46426536	snp	A/G			intron-variant	Hck	Mm_Celera	2:153118920	CATCTTCATGGGTTA[A/G]CAAACTCAATCCTGA	15162
rs46441905	snp	A/G			intron-variant	Hck	Mm_Celera	2:153142813	CGTGTTTATCAGTTT[A/G]TATTAACTAAGCTGC	15162
rs46465103	snp	C/G			intron-variant	Hck	Mm_Celera	2:153136555	AGACAGCCCAGAGAA[C/G]GTAGGTATTTCAGTT	15162
rs46497805	snp	A/C			intron-variant	Hck	Mm_Celera	2:153121323	TCTGGAGCTGAGAGC[A/C]ATAGTCAGGAATGCA	15162
rs46510765	snp	G/T			intron-variant	Hck	Mm_Celera	2:153135581	GAAAAGCATGTATAA[G/T]ACCAGAGCCACTAAA	15162
rs46514989	snp	A/C			intron-variant	Hck	Mm_Celera	2:153118884	AAATTGAAGGAGATG[A/C]TAGAAGAGGGAGAGA	15162
rs46545912	snp	C/G/T			intron-variant	Hck	Mm_Celera	2:153123937	ACCCATGCTGCTCCA[C/G/T]AGATCCGTCGTGCCA	15162
rs46580434	snp	C/T			intron-variant	Hck	Mm_Celera	2:153149851	GATCAAGGTGGCACA[C/T]GGGCAGCTGGGGCAG	15162
rs46587745	snp	A/G			intron-variant	Hck	Mm_Celera	2:153150594	ACCTTAAGAGGTCTG[A/G]CATTGCCAGATACTG	15162
rs46657520	snp	C/T			intron-variant	Hck	Mm_Celera	2:153123487	TTGACTTAACAAGCC[C/T]CTATTTTTCCACCAT	15162
rs46676588	snp	C/T			intron-variant	Hck	Mm_Celera	2:153128119	CTATCCATGTACAGA[C/T]TCTGTTCTTTATCAT	15162
rs46706144	snp	A/C/T			intron-variant	Hck	GRCm38.p3	2:153143936	AGGTCCTGAGTTCAA[A/C/T]TCCCAGCAACCACAT	15162
rs46754907	snp	A/G			intron-variant	Hck	Mm_Celera	2:153136150	GAGGTGACCTTGGTG[A/G]ATGACAAGGACAGAA	15162
rs46762003	snp	C/T			intron-variant	Hck	Mm_Celera	2:153117034	GATGGGCCTAGAGTA[C/T]AAATGCTTTCAGAAC	15162
rs46784472	snp	A/G			intron-variant	Hck	Mm_Celera	2:153128118	TCTATCCATGTACAG[A/G]CTCTGTTCTTTATCA	15162
rs46805724	snp	C/G			intron-variant	Hck	Mm_Celera	2:153120379	GTATATACCCGAAGG[C/G]TTGGAAGCCAACACA	15162
rs46851550	snp	G/T			intron-variant	Hck	Mm_Celera	2:153126721	GTGCTTGCATTGCAA[G/T]CTTAACTGCCTGAGT	15162
rs46874398	snp	A/G			intron-variant	Hck	Mm_Celera	2:153131694	CTTGACCCAAAACAG[A/G]ACCTGGCCCTGTGCC	15162
rs46928377	snp	A/C			intron-variant	Hck	Mm_Celera	2:153143503	CCTTCCCAAGCTCAG[A/C]TTTCCCACCTCTGCT	15162
rs46982439	snp	A/C			intron-variant	Hck	Mm_Celera	2:153124908	GTTACTTTTCTATTA[A/C]TGTGATAAAATGCCA	15162
rs47001684	snp	A/G			intron-variant	Hck	Mm_Celera	2:153116737	CCAGAAGAGGGCGTC[A/G]GATCTTGTTACAGAT	15162
rs47015849	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153108150	TTACAATTCTTTAGG[A/G]AATCCAAGGGTATTT	15162
rs47032588	snp	A/G			intron-variant	Hck	GRCm38.p3	2:153131695	TTGACCCAAAACAGG[A/G]CCTGGCCCTGTGCCT	15162
rs47088178	snp	C/T			intron-variant	Hck	Mm_Celera	2:153137272	ACAGAATCATGACAA[C/T]GTCCGTGTTGTCACT	15162
rs47096059	snp	C/T			intron-variant	Hck	Mm_Celera	2:153124680	GGCAGAGACACAGCA[C/T]CTCCAGAGTAAGCTG	15162
rs47129198	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153107988	GCCAAGCGTGGCTGC[C/T]TGAGTTCAGTCCCCG	15162
rs47130203	snp	A/G			intron-variant	Hck	Mm_Celera	2:153114416	TTGTCAGTACAGCTC[A/G]CCTCCCTGTTCCAGC	15162
rs47148055	snp	A/G			intron-variant	Hck	Mm_Celera	2:153125011	GGAGCAGAGCCAGCC[A/G]CTGGCAGCCATGGCA	15162
rs47210566	snp	A/G			intron-variant	Hck	Mm_Celera	2:153147368	GAACAAAACAGACCC[A/G]GCCGAGCTGATGTGT	15162
rs47268648	snp	C/T			intron-variant	Hck	Mm_Celera	2:153147113	ATATTTCCTTTAGGG[C/T]TGAGACTTGTCAATA	15162
rs47288287	snp	C/T			intron-variant	Hck	Mm_Celera	2:153150883	CCCCTCCCTAACACA[C/T]ACACACACACACACA	15162
rs47306234	snp	A/G			intron-variant	Hck	Mm_Celera	2:153146894	CTTCTCATCTCTGCT[A/G]GGATTTTGTCCAGTT	15162
rs47320356	snp	A/C			intron-variant	Hck	Mm_Celera	2:153144944	CCCAGGAAACAAAAC[A/C]AGAACCATGTGAATG	15162
rs47364906	snp	A/G			intron-variant	Hck	Mm_Celera	2:153121702	TTCTACATCGGTGGT[A/G]ATGTTATCAGTCAAT	15162
rs47376709	snp	C/T			intron-variant	Hck	Mm_Celera	2:153146854	GCCACAACTGCTCAG[C/T]TAGGGGTGGGACTTC	15162
rs47377896	snp	A/G			intron-variant	Hck	Mm_Celera	2:153136942	CAAGATGGCCTTGGC[A/G]TGGCTCTTCTGGCAC	15162
rs47408934	snp	A/C/G			intron-variant	Hck	GRCm38.p3	2:153150346	TGGCTTTGGGGGGGC[A/C/G]GGTACACTAGTAAAA	15162
rs47423813	snp	A/C			intron-variant	Hck	Mm_Celera	2:153114452	AGGCCACAATCACAG[A/C]CAGCCAGCATCTCCG	15162
rs47453496	snp	A/G			intron-variant	Hck	Mm_Celera	2:153125128	CAGCTCCCACCCCCA[A/G]TGGCATGCTTCCTTA	15162
rs47459097	snp	C/T			intron-variant	Hck	Mm_Celera	2:153147944	GCAGCAGAGAGTGAT[C/T]GAGAGCCTGGTCATT	15162
rs47479128	snp	G/T			intron-variant	Hck	Mm_Celera	2:153145269	TGATCGCCCCAGACT[G/T]AAACACTGTAACTGA	15162
rs47513421	snp	A/G			intron-variant	Hck	Mm_Celera	2:153123368	CTGCTGTCACCCGTG[A/G]CTGGACAATCACAGC	15162
rs47548262	snp	A/T			intron-variant	Hck	Mm_Celera	2:153146679	TCAGGACCAGTTTTT[A/T]AAAAGAAAAGGAGTG	15162
rs47567352	snp	A/T			intron-variant	Hck	Mm_Celera	2:153139606	GCAGAGTGTGTCATT[A/T]AAAAAAAAAAAAAAA	15162
rs47621264	snp	C/T			intron-variant	Hck	Mm_Celera	2:153135510	CCCCCATGCTCTCAC[C/T]ACAAACACCACAGAT	15162
rs47622742	snp	A/G			intron-variant	Hck	GRCm38.p3	2:153136134	GTTTGAGCATGTGTT[A/G]GAGGTGACCTTGGTG	15162
rs47630980	snp	A/G			intron-variant	Hck	Mm_Celera	2:153139538	TGAATGACTGAAATC[A/G]TAACAGTCAGGAAGC	15162
rs47651808	snp	C/T			intron-variant	Hck	Mm_Celera	2:153122208	CTCAGCGGTAGGGTT[C/T]TTGCTGGACATTCAT	15162
rs47672532	snp	A/G			intron-variant	Hck	Mm_Celera	2:153121291	GAGACAATGGACACG[A/G]AGCAATCAGAGTTTA	15162
rs47778089	snp	A/G			intron-variant	Hck	Mm_Celera	2:153118761	TTGAAAACTAAATCA[A/G]GAAAAAAAAAATCCT	15162
rs47783181	snp	C/T			intron-variant	Hck	Mm_Celera	2:153144896	AGACTTCAGCAAGTG[C/T]AGGTCGAGGTGAGAG	15162
rs47817027	snp	C/T			intron-variant	Hck	Mm_Celera	2:153138950	GGACTGAATCCAGGA[C/T]CTCTGGAAGAGCAGC	15162
rs47849021	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120924	AATAAAACTCCCTCC[A/G]CCCCTCCTGCTCCAG	15162
rs47853315	snp	C/T			intron-variant	Hck	Mm_Celera	2:153140077	CCAACTCCTGCTCTC[C/T]GCTCTCTGGGGGGAA	15162
rs47854483	snp	C/T			synonymous-codon	Hck	Mm_Celera	2:153136756	GCCAGGGAGCATGTC[C/T]GTGGAGGCCTTCCTG	15162
rs47857624	snp	A/C			intron-variant	Hck	Mm_Celera	2:153138699	CTGTGCGGTTGGTTG[A/C]GTGCAGATGCAGAAC	15162
rs47869591	snp	G/T			intron-variant	Hck	Mm_Celera	2:153130809	GCTGTGTTGGGGTGG[G/T]GGTGGGAAACTATGA	15162
rs47906342	snp	C/G			intron-variant	Hck	Mm_Celera	2:153121363	CACCCCAAATTCCAT[C/G]TTCCAACATGGAAGT	15162
rs47927964	snp	A/G			intron-variant	Hck	Mm_Celera	2:153137564	CCCTGGTCATTTCTG[A/G]ATAAACATCTCATAC	15162
rs47958225	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120326	CCTCAAAACCCTAAA[A/G]CTAGAGCTACCATGT	15162
rs47967627	snp	A/G			intron-variant	Hck	Mm_Celera	2:153146689	TTTTTTAAAAGAAAA[A/G]GAGTGGCAAATTGGC	15162
rs47976110	snp	A/G			intron-variant	Hck	Mm_Celera	2:153146774	CATGTAGTGGAAGGA[A/G]AGCACTGACTCCTGC	15162
rs47991596	snp	C/T			intron-variant	Hck	Mm_Celera	2:153141410	TCTGCACGCAACCAA[C/T]CGCACAGCAAGAATA	15162
rs48001842	snp	A/G			intron-variant	Hck	Mm_Celera	2:153124601	GGAGGCTGAGGGATC[A/G]CTCAGTAGATAAAGA	15162
rs48014850	snp	C/T			intron-variant	Hck	GRCm38.p3	2:153149909	GTGGTAGCACATGGG[C/T]AGCTGGGGCAGGTGG	15162
rs48052825	snp	A/G			intron-variant	Hck	Mm_Celera	2:153114479	TCCGAAGGTTCTGGG[A/G]TTTAAACTCTGATCC	15162
rs48062096	snp	C/T			intron-variant	Hck	Mm_Celera	2:153143541	CTGGCTCTATGTTAC[C/T]CTAGGATCGCTGGTC	15162
rs48101622	snp	A/C			intron-variant	Hck	Mm_Celera	2:153144903	AGCAAGTGCAGGTCG[A/C]GGTGAGAGGTGAGAA	15162
rs48141298	snp	A/C			intron-variant	Hck	Mm_Celera	2:153120295	TGTAGCCACCATGGA[A/C]GTCAATATGAAGGTT	15162
rs48151298	snp	A/C			intron-variant	Hck	Mm_Celera	2:153137311	CTTAGCTTTGGGCCA[A/C]TGTATCCTGGGATTA	15162
rs48154319	snp	C/T			intron-variant	Hck	Mm_Celera	2:153141754	CCTAGGTTGGAGAGA[C/T]GGTTCGGTGGTTGAG	15162
rs48171472	snp	C/T			intron-variant	Hck	Mm_Celera	2:153148602	AAGTCCTCTCCTGCA[C/T]GCCATAGCTGGGGAG	15162
rs48177088	snp	C/T			intron-variant	Hck	Mm_Celera	2:153113986	ATGGGAGTTTAGCAC[C/T]CAACACCGTGTCAGG	15162
rs48197711	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130389	AAAGGCGATGATCAC[A/G]TATAAGCTCTTGATG	15162
rs48236125	snp	A/G			intron-variant	Hck	Mm_Celera	2:153135153	CCAGTGACATTCCAG[A/G]CATGATGGGACACCA	15162
rs48384932	snp	A/T			intron-variant	Hck	Mm_Celera	2:153118997	CCATAAAAACCCCAA[A/T]GGCATCCTTCACAGA	15162
rs48428581	snp	G/T			intron-variant	Hck	Mm_Celera	2:153136556	GACAGCCCAGAGAAG[G/T]TAGGTATTTCAGTTG	15162
rs48438974	snp	A/C			intron-variant	Hck	GRCm38.p3	2:153149891	CATGGGTACCTGGGG[A/C]AGGTGGTAGCACATG	15162
rs48445755	snp	A/G			intron-variant	Hck	Mm_Celera	2:153135412	CATAAGGAAGTGCAA[A/G]GAAGAAAGACAGATC	15162
rs48448343	snp	A/G			intron-variant	Hck	Mm_Celera	2:153137277	ATCATGACAATGTCC[A/G]TGTTGTCACTTCAGG	15162
rs48453973	snp	A/G			intron-variant	Hck	Mm_Celera	2:153135610	AATGAAGCAGGGTGG[A/G]ATGGAGCAAGAGAAC	15162
rs48474256	snp	C/T			intron-variant	Hck	Mm_Celera	2:153146552	CTCCCAATCATCTAA[C/T]CCTAGTTCCATGGTT	15162
rs48478256	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153107815	TCTAGAACACACAAG[C/T]GCGCGCGCGCGCGCT	15162
rs48554565	snp	A/G			intron-variant	Hck	Mm_Celera	2:153121580	TCAATACTTTCCAGA[A/G]GGTTTATATCTCTTA	15162
rs48568348	snp	G/T			intron-variant	Hck	Mm_Celera	2:153136286	TAACTGGTGGCTTAA[G/T]GGTTACTACCCAGGG	15162
rs48587658	snp	C/T			intron-variant	Hck	Mm_Celera	2:153116892	AGGAGAACTGGGGAG[C/T]TGCTGCTAATGGTGG	15162
rs48592548	snp	G/T			intron-variant	Hck	Mm_Celera	2:153143879	AGGAGACAAGGGCTG[G/T]AGAGTTGGATCAGAG	15162
rs48593414	snp	C/T			intron-variant	Hck	Mm_Celera	2:153136246	AGCGTTAAGCTTACA[C/T]GCTATGCAGGCTCAT	15162
rs48597686	snp	A/G			intron-variant	Hck	Mm_Celera	2:153147369	AACAAAACAGACCCG[A/G]CCGAGCTGATGTGTC	15162
rs48614951	snp	C/T			intron-variant	Hck	Mm_Celera	2:153138619	AAACAGTTATTATTT[C/T]GTATTGTATAAGAGA	15162
rs48640428	snp	C/T			intron-variant	Hck	Mm_Celera	2:153139975	TGGGTGCACACACCC[C/T]GGGTTCTGTTCCCAA	15162
rs48651995	snp	C/T			intron-variant	Hck	Mm_Celera	2:153119848	TGTAAGATTAAAAGG[C/T]TCTGCAGTCTGTGGA	15162
rs48672379	snp	A/G			intron-variant	Hck	Mm_Celera	2:153132432	TTTAGGCTACAGGGA[A/G]GCCCAGCTTGTCTCC	15162
rs48724302	snp	C/T			intron-variant	Hck	Mm_Celera	2:153130224	ACTGTCTGCCTCCCT[C/T]CCTCTTGAGTGTTGA	15162
rs48727381	snp	G/T			upstream-variant-2KB	Hck	Mm_Celera	2:153108190	GGTAGGGGTCCAAAA[G/T]CTCTGGGGATAGGGT	15162
rs48758517	snp	A/G			intron-variant	Hck	Mm_Celera	2:153139250	CATGTCCAAGGTGAC[A/G]TTCATTCTTACAACT	15162
rs48816196	snp	C/T			intron-variant	Hck	Mm_Celera	2:153116816	GAGCAGTCGGGTGCT[C/T]TTACCCACTGAGCCA	15162
rs48825690	snp	C/T			intron-variant	Hck	Mm_Celera	2:153144924	GAGGTGAGAATAATG[C/T]TATGCCCAGGAAACA	15162
rs48827586	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130414	TTGATGAGTTGGGGC[A/G]GAAGTCAGTGGTTAA	15162
rs48833985	snp	C/T			intron-variant	Hck	Mm_Celera	2:153120245	AAATGCCAGTGAGGC[C/T]GTGGGGAAAGTCGAT	15162
rs48920657	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118554	CAGGTTAGCCTTGAA[C/T]TCATGTTGTTCCTCC	15162
rs48922592	snp	C/T			intron-variant	Hck	Mm_Celera	2:153136086	CTCAGTGGTAGAGCA[C/T]TTTCCTAGTATGAGA	15162
rs49022702	snp	A/G			intron-variant	Hck	Mm_Celera	2:153147025	TGTCTATGGCTTTAC[A/G]ATCTCTCTACTGCCT	15162
rs49028634	snp	A/C			intron-variant	Hck	Mm_Celera	2:153148669	AGCCCCCCGGAGATC[A/C]CTTATCCCCAAAGAC	15162
rs49032241	snp	A/G			intron-variant	Hck	Mm_Celera	2:153121653	GAGTCAAGATCACCT[A/G]TAATTAGGCTCTGGA	15162
rs49099148	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118703	AGGCTAAAAGGTCAA[C/T]ATTGAAAATCAGTAG	15162
rs49106151	snp	A/G			intron-variant	Hck	Mm_Celera	2:153147478	AGAGTAGCACAGGGG[A/G]AAAGCCTCCATTGCT	15162
rs49151887	snp	C/T			intron-variant	Hck	Mm_Celera	2:153135145	CACAATGTCCAGTGA[C/T]ATTCCAGGCATGATG	15162
rs49157790	snp	C/T			intron-variant	Hck	Mm_Celera	2:153122198	GGGGACATAGCTCAG[C/T]GGTAGGGTTTTTGCT	15162
rs49163539	snp	C/G			intron-variant	Hck	Mm_Celera	2:153124098	AGGCTGTCAGGCAGG[C/G]TGGGAAAGTGAAGAC	15162
rs49191889	snp	A/C			intron-variant	Hck	Mm_Celera	2:153121233	GAATGAGTCACCAAA[A/C]GCTCTCAGGTCAGCT	15162
rs49251307	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130799	ATAATAAAATGCTGT[A/G]TTGGGGTGGTGGTGG	15162
rs49266883	snp	A/C			intron-variant	Hck	Mm_Celera	2:153138684	TTTAGAATATTCTTG[A/C]TGTGCGGTTGGTTGC	15162
rs49270941	snp	G/T			intron-variant	Hck	Mm_Celera	2:153116684	AAAGATTTATTTATT[G/T]ATTATATGTAAGTAC	15162
rs49275475	snp	G/T			intron-variant	Hck	Mm_Celera	2:153124778	GGGGCTCCACACATG[G/T]ATGTACCCATGTAGA	15162
rs49295209	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120858	GCCACCATTATCATC[A/G]TCCACCTTAATATCC	15162
rs49301549	snp	G/T			intron-variant	Hck	Mm_Celera	2:153136959	GGCTCTTCTGGCACA[G/T]CCACCTCATAGAGCA	15162
rs49303692	snp	A/G			intron-variant	Hck	Mm_Celera	2:153145013	ACAATGTAGCACCAC[A/G]CAGCAGTTAAGGACC	15162
rs49321067	snp	C/G			intron-variant	Hck	Mm_Celera	2:153117025	TTTGGCAATGATGGG[C/G]CTAGAGTACAAATGC	15162
rs49327497	snp	G/T			intron-variant	Hck	Mm_Celera	2:153131893	GACATGCATGTCCCC[G/T]ACCCCATAAGATGTA	15162
rs49352620	snp	C/T			intron-variant	Hck	Mm_Celera	2:153128980	GGGGCTGCTCTGGTG[C/T]AAAGGAGTCGGGAAC	15162
rs49362549	snp	A/T			intron-variant	Hck	Mm_Celera	2:153121379	TTCCAACATGGAAGT[A/T]GTCTCATGAAGTTTT	15162
rs49424801	snp	A/T			intron-variant	Hck	Mm_Celera	2:153130758	TAGCCTGGTCTACAT[A/T]GTGAGATCCAGGACA	15162
rs49528831	snp	A/T			intron-variant	Hck	Mm_Celera	2:153139533	AATGGTGAATGACTG[A/T]AATCGTAACAGTCAG	15162
rs49620164	snp	C/T			intron-variant	Hck	Mm_Celera	2:153143500	CAGCCTTCCCAAGCT[C/T]AGATTTCCCACCTCT	15162
rs49629355	snp	G/T			intron-variant	Hck	Mm_Celera	2:153148541	AGGAAGGGAAGAATA[G/T]GAAGGAAGGGACACT	15162
rs49651140	snp	A/G			intron-variant	Hck	Mm_Celera	2:153121456	TTCATCAGTGGGCTC[A/G]TGAATTAGGTGGCTA	15162
rs49685092	snp	G/T			intron-variant	Hck	Mm_Celera	2:153118900	TAGAAGAGGGAGAGA[G/T]CCTCCATCTTCATGG	15162
rs49715359	snp	A/C			intron-variant	Hck	Mm_Celera	2:153121296	AATGGACACGGAGCA[A/C]TCAGAGTTTATTCTG	15162
rs49718156	snp	A/G			intron-variant	Hck	Mm_Celera	2:153137044	GGAGAGGAGGGGCAG[A/G]GGCTGCAGAGCCTCT	15162
rs49744459	snp	C/G			intron-variant	Hck	Mm_Celera	2:153132056	CCGCAAAGGCAGGGG[C/G]ATCTCTAAGTTCAGG	15162
rs49756801	snp	A/C/T			intron-variant	Hck	Mm_Celera	2:153121701	TTTCTACATCGGTGG[A/C/T]GATGTTATCAGTCAA	15162
rs49766787	snp	C/T			intron-variant	Hck	Mm_Celera	2:153116720	AGCTGTCTTCAGACA[C/T]TCCAGAAGAGGGCGT	15162
rs49771060	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153108153	CAATTCTTTAGGGAA[C/T]CCAAGGGTATTTGGT	15162
rs49788438	snp	C/T			intron-variant	Hck	GRCm38.p3	2:153150155	CTAAGATATTTAAAG[C/T]TTCTTGTTTTTGCTC	15162
rs49835627	snp	A/G			downstream-variant-500B	Hck	GRCm38.p3	2:153151758	AAGGAGATGGCTGGC[A/G]CTCTGGAGAATGACA	15162
rs49913816	snp	C/T			intron-variant	Hck	Mm_Celera	2:153135593	TAATACCAGAGCCAC[C/T]AAATGAAGCAGGGTG	15162
rs49930577	snp	G/T			intron-variant	Hck	Mm_Celera	2:153124846	GAACACATATAAACA[G/T]ACATCATATGCATGC	15162
rs49962393	snp	C/G			intron-variant	Hck	GRCm38.p3	2:153149884	GGTGGCACATGGGTA[C/G]CTGGGGCAGGTGGTA	15162
rs50030117	snp	A/G			intron-variant	Hck	Mm_Celera	2:153148620	CATAGCTGGGGAGTG[A/G]ATGGGGTGAGGTATC	15162
rs50039840	snp	A/G			intron-variant	Hck	Mm_Celera	2:153117829	ACACACTTAAAGCAT[A/G]CACTTCATCCGTGTT	15162
rs50040400	snp	A/C			intron-variant	Hck	Mm_Celera	2:153118527	GGCTGGCCTTGAACT[A/C]TCTATGTAGCTCAGG	15162
rs50082699	snp	C/T			intron-variant	Hck	Mm_Celera	2:153137479	GTGTGTCTCCACACC[C/T]GGCTTCTCAGAGTTA	15162
rs50103585	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153108448	AGGGCGGAGTCGGGG[C/T]ATTTGGGGGCGGGGT	15162
rs50123094	snp	C/T			intron-variant	Hck	Mm_Celera	2:153136975	CCACCTCATAGAGCA[C/T]CTACACTCCAGCCTC	15162
rs50191333	snp	A/C			upstream-variant-2KB	Hck	Mm_Celera	2:153106592	GCACATTGTTAACCG[A/C]GATGTTAGGGATGCT	15162
rs50193622	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120374	TCTGGGTATATACCC[A/G]AAGGGTTGGAAGCCA	15162
rs50254169	snp	A/G			intron-variant	Hck	Mm_Celera	2:153149899	CCTGGGGCAGGTGGT[A/G]GCACATGGGCAGCTG	15162
rs50303022	snp	A/G			intron-variant	Hck	Mm_Celera	2:153136993	ACACTCCAGCCTCCT[A/G]GCTGGCAGAGTGCAA	15162
rs50308425	snp	A/G			intron-variant	Hck	Mm_Celera	2:153123335	ATAGATGGGGTTCTA[A/G]CCCCTCAGGCCCCAG	15162
rs50330781	snp	A/G			intron-variant	Hck	Mm_Celera	2:153128097	CCGATCACATTTTAA[A/G]ATAGCTCTATCCATG	15162
rs50360251	snp	C/T			intron-variant	Hck	Mm_Celera	2:153145374	AACAGAGACAACTGT[C/T]GGAAACCCTGGGAGC	15162
rs50366916	snp	C/T			intron-variant	Hck	Mm_Celera	2:153122839	TGGTCAGATGCGATG[C/T]ACTGTGTTCAGGGGC	15162
rs50410210	snp	C/T			intron-variant	Hck	Mm_Celera	2:153139087	ACTACATTTGAGCTA[C/T]GTCACCATCCATGTA	15162
rs50441395	snp	G/T			intron-variant	Hck	Mm_Celera	2:153150162	ATTTAAAGTTTCTTG[G/T]TTTTGCTCTTAATCA	15162
rs50468722	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118622	GTTTATGATCCTACA[C/T]CTAAAAGCCTCTACA	15162
rs50479337	snp	A/G			intron-variant	Hck	Mm_Celera	2:153143911	TTAAGAGCACTGACT[A/G]CTCTTCCAGAGGTCC	15162
rs50503882	snp	A/G			intron-variant	Hck	Mm_Celera	2:153139344	GGACCTGTCCAAGGT[A/G]CAAGCAGTGGGTAAG	15162
rs50507432	snp	A/G			intron-variant	Hck	Mm_Celera	2:153136265	ATGCAGGCTCATGTT[A/G]CAGTCTAACTGGTGG	15162
rs50521545	snp	C/T			intron-variant	Hck	Mm_Celera	2:153120859	CCACCATTATCATCG[C/T]CCACCTTAATATCCT	15162
rs50540626	snp	A/G			intron-variant	Hck	Mm_Celera	2:153144000	GCCCTCTTCTGGTGC[A/G]TCTGAAAACAGCAAC	15162
rs50560554	snp	C/T			intron-variant	Hck	Mm_Celera	2:153145983	ATCACAAGTTCAAGG[C/T]CTGCCAGGGTAGTTA	15162
rs50580395	snp	A/G			intron-variant	Hck	Mm_Celera	2:153115633	ACTTTTACTCCACCT[A/G]AAAATGAAGGGCTGA	15162
rs50583871	snp	A/G			intron-variant	Hck	Mm_Celera	2:153139673	CAGGGAGGCTCTGCA[A/G]CTGGCCTAAGCTGCA	15162
rs50630508	snp	A/G			intron-variant	Hck	Mm_Celera	2:153124967	TTTATTTAGGCTCAC[A/G]GGTCCAGAGGCTTAG	15162
rs50647686	snp	A/G			intron-variant	Hck	Mm_Celera	2:153117460	TGAACCCCACTACAC[A/G]GGGGGGGGGGTGAAC	15162
rs50661911	snp	C/T			intron-variant	Hck	Mm_Celera	2:153122418	GCTGCATGCTTACAG[C/T]TGCATCTGTCACTGC	15162
rs50680972	snp	A/G			intron-variant	Hck	Mm_Celera	2:153139005	CTCTCCAGATTCTGG[A/G]ATAATTTTGTTTGTT	15162
rs50711410	snp	C/T			intron-variant	Hck	GRCm38.p3	2:153144925	AGGTGAGAATAATGC[C/T]ATGCCCAGGAAACAA	15162
rs50736629	snp	C/T			intron-variant	Hck	Mm_Celera	2:153146575	CCATGGTTCCAATAC[C/T]CTCTTTTGGATGCTG	15162
rs50752245	snp	A/C/G			intron-variant	Hck	Mm_Celera	2:153113722	CAGCTTGTGAGAATC[A/C/G]TCTCTCTCCTTCCAC	15162
rs50771673	snp	A/G			intron-variant	Hck	Mm_Celera	2:153134500	TGGCCTGGACAGGCA[A/G]TCACGCTGGGCACCC	15162
rs50937653	snp	A/G			intron-variant	Hck	Mm_Celera	2:153147941	GTGGCAGCAGAGAGT[A/G]ATTGAGAGCCTGGTC	15162
rs51036337	snp	C/T			intron-variant	Hck	Mm_Celera	2:153122241	TGTCCTGGGTTCCAT[C/T]CACAGCACCAGGAAA	15162
rs51037623	snp	C/G/T			intron-variant	Hck	GRCm38.p3	2:153117956	TGGATTCAAAAAGTG[C/G/T]CTTTAATGAAGTTTA	15162
rs51073259	snp	A/G			intron-variant	Hck	Mm_Celera	2:153146265	TCTCTAGATGTGGCT[A/G]AGGATGTGGCTTGGT	15162
rs51082871	snp	A/C			intron-variant	Hck	Mm_Celera	2:153120324	TTCCTCAAAACCCTA[A/C]AGCTAGAGCTACCAT	15162
rs51106509	snp	C/T			intron-variant	Hck	Mm_Celera	2:153117360	TACCACAGCCTTTGT[C/T]TCCGAAGACCTCAAG	15162
rs51111822	snp	G/T			intron-variant	Hck	Mm_Celera	2:153139227	ATGCACTGAGGTGGC[G/T]TGAGGAGCATGTCCA	15162
rs51132055	snp	A/G			intron-variant	Hck	Mm_Celera	2:153141697	GGATTAAAGGTGTGC[A/G]CCACCACGCCCGGCT	15162
rs51157682	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130238	TCCCTCTTGAGTGTT[A/G]AGCTCTCACACCTGC	15162
rs51167344	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153108171	AAGGGTATTTGGTCT[C/T]TTAGGTAGGGGTCCA	15162
rs51167663	snp	C/G			intron-variant	Hck	Mm_Celera	2:153119776	GACTCGAACCTGCTG[C/G]GAAAAGCACAGGCGA	15162
rs51176374	snp	C/T			intron-variant	Hck	Mm_Celera	2:153113791	TGGCAGGAGGTGCCT[C/T]TGCCCTCAGCCCTAA	15162
rs51222429	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130333	GACAAGCCCCTTATC[A/G]TCTCTGTTCTCTGCT	15162
rs51244013	snp	C/T			intron-variant	Hck	Mm_Celera	2:153146646	GGCAAAATGCCCCTA[C/T]ATGTAAAATAAGTCA	15162
rs51277116	snp	A/G			intron-variant	Hck	Mm_Celera	2:153118947	CTGAGACAATGCTAA[A/G]TTACCAAAAGCAATC	15162
rs51287607	snp	C/T			intron-variant	Hck	Mm_Celera	2:153138718	CAGATGCAGAACCCA[C/T]GGATACAGACTGTTC	15162
rs51301858	snp	A/T			intron-variant	Hck	Mm_Celera	2:153140242	GCATTCTAGACAAAA[A/T]GAAACAGCCTGTTCA	15162
rs51307336	snp	G/T			intron-variant	Hck	Mm_Celera	2:153143817	GGATTTTTGTTGGAT[G/T]AGAGGGCGAATTTTC	15162
rs51310870	snp	A/C			intron-variant	Hck	Mm_Celera	2:153134493	GACTTCCTGGCCTGG[A/C]CAGGCAATCACGCTG	15162
rs51326796	snp	A/G			intron-variant	Hck	Mm_Celera	2:153150478	GATGGCCAGAGCTAC[A/G]TAGTAAGACCCTGTC	15162
rs51326984	snp	A/G			intron-variant	Hck	Mm_Celera	2:153141241	ATTATCCCAGGACCT[A/G]GAGAGATGGCTCAGT	15162
rs51388183	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130814	GTTGGGGTGGTGGTG[A/G]GAAACTATGAATGTT	15162
rs51420201	snp	A/C			intron-variant	Hck	Mm_Celera	2:153145232	AGGCAAAAGTCATCT[A/C]TGAAGGTCACAGTGT	15162
rs51433426	snp	C/T			intron-variant	Hck	Mm_Celera	2:153144710	ACAGCCCATGGAAGG[C/T]TCTACCCACATTCAG	15162
rs51448079	snp	C/T			intron-variant	Hck	Mm_Celera	2:153117407	AGGGCTTCCTCCTTA[C/T]AGAGAGGAAAACGAA	15162
rs51497745	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130422	TTGGGGCAGAAGTCA[A/G]TGGTTAAGAACACTG	15162
rs51514324	snp	C/T			intron-variant	Hck	Mm_Celera	2:153119528	ATCTGCCCAAGAACC[C/T]ACAGTTGGGGGAGCT	15162
rs51518612	snp	C/G			intron-variant	Hck	Mm_Celera	2:153122841	GTCAGATGCGATGTA[C/G]TGTGTTCAGGGGCTA	15162
rs51522791	snp	A/G			intron-variant	Hck	Mm_Celera	2:153137142	GAAGTCTTGCTCCAA[A/G]TTCTAAGGGACAAGA	15162
rs51523150	snp	A/G			synonymous-codon	Hck	Mm_Celera	2:153136864	CTTTATTGTCACGGA[A/G]TTCATGGCCAAAGGT	15162
rs51585003	snp	A/T			intron-variant	Hck	Mm_Celera	2:153118872	CACCGAAGAAAGAAA[A/T]TGAAGGAGATGCTAG	15162
rs51618849	snp	A/T			intron-variant	Hck	Mm_Celera	2:153135966	GATATATGCCTACCA[A/T]CCCAGCTATATATTG	15162
rs51621360	snp	A/G			intron-variant	Hck	Mm_Celera	2:153135431	GAAAGACAGATCTGA[A/G]AAGCAAAGCTGGGAC	15162
rs51622016	snp	A/G			synonymous-codon	Hck	Mm_Celera	2:153136861	CATCTTTATTGTCAC[A/G]GAGTTCATGGCCAAA	15162
rs51707234	snp	C/T			intron-variant	Hck	Mm_Celera	2:153120257	GGCCGTGGGGAAAGT[C/T]GATGCTGATGGGTGT	15162
rs51715403	snp	C/T			intron-variant	Hck	Mm_Celera	2:153126248	GAGCAGGTGTGTCCC[C/T]GGCAATCTTCACTTG	15162
rs51750172	snp	A/G/T			intron-variant	Hck	GRCm38.p3	2:153147391	TGATGTGTCATCACC[A/G/T]CTGCCAGGAAGTTGA	15162
rs51766536	snp	A/G			intron-variant	Hck	Mm_Celera	2:153118928	TGGGTTAACAAACTC[A/G]ATCCTGAGACAATGC	15162
rs51796469	snp	A/G			intron-variant	Hck	Mm_Celera	2:153134531	CTGAAGGTTTAGGCT[A/G]GCTGGACATGAGGGT	15162
rs51805498	snp	C/T			intron-variant	Hck	Mm_Celera	2:153135471	AAACAAACAAACAAA[C/T]AAACAAAAAACTGTC	15162
rs51820962	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153107211	ACATAGTACTGCTAA[A/G]CGCATGCCTACATGC	15162
rs51829585	snp	A/C			intron-variant	Hck	Mm_Celera	2:153130281	GACTGCCTAGGTTCT[A/C]ATCCTGACTCTTCCA	15162
rs51838709	snp	C/G			intron-variant	Hck	Mm_Celera	2:153120156	AGGCAGGGGAACTGT[C/G]GTGAGTGAGTTTTAG	15162
rs51843664	snp	A/T			intron-variant	Hck	Mm_Celera	2:153121492	AAGTGGGAGAATCTC[A/T]GCTATGGGCTTCAGA	15162
rs51853166	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153106590	TGGCACATTGTTAAC[C/T]GAGATGTTAGGGATG	15162
rs51897631	snp	A/G			intron-variant	Hck	Mm_Celera	2:153131858	GAAGATTGTCCTCTG[A/G]CCTCTACAAGCATGA	15162
rs51901789	snp	C/T			intron-variant	Hck	Mm_Celera	2:153146648	CAAAATGCCCCTACA[C/T]GTAAAATAAGTCATT	15162
rs51917477	snp	A/G			intron-variant	Hck	Mm_Celera	2:153138792	AATTTTTCATAACAG[A/G]TTAATTATTTTATTA	15162
rs51927978	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120519	AATGGAGTATTACTC[A/G]TCTGTAAAGAAGAAT	15162
rs51960302	snp	C/T			intron-variant	Hck	Mm_Celera	2:153134533	GAAGGTTTAGGCTGG[C/T]TGGACATGAGGGTGG	15162
rs52004126	snp	A/G			intron-variant	Hck	Mm_Celera	2:153114721	TGTGGCGCTGGGGAC[A/G]GAACCCAGGGCTCTG	15162
rs52017107	snp	A/G			intron-variant	Hck	Mm_Celera	2:153137341	ATTCAGCATATTTCA[A/G]GAATGTTTGAGAAAG	15162
rs52032925	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118672	TAGCCCTAATAAATG[C/T]TTCCAGCTAAGTAGC	15162
rs52042948	snp	A/G			intron-variant	Hck	Mm_Celera	2:153113771	CAAACTCAGGTCATC[A/G]GACTTGGCAGGAGGT	15162
rs52051785	snp	C/T			intron-variant	Hck	Mm_Celera	2:153134801	TGGGGCCAGAGTCCA[C/T]AAAGCCAGAGCTGGG	15162
rs52102569	snp	C/T			intron-variant	Hck	Mm_Celera	2:153135921	TTTTTTAAAAGAAAG[C/T]AAGAGTGAATTTATT	15162
rs52130352	snp	A/T			intron-variant	Hck	Mm_Celera	2:153135804	AGAGGGAACTGCTGG[A/T]AAAGATCATCCTCTG	15162
rs52132330	snp	A/G			intron-variant	Hck	Mm_Celera	2:153117725	AAGGAAGGAAGGAAG[A/G]AAGGAAGAAAGAAAA	15162
rs52139298	snp	C/T			intron-variant	Hck	GRCm38.p3	2:153149882	GTGGTGGCACATGGG[C/T]ACCTGGGGCAGGTGG	15162
rs52158510	snp	C/T			intron-variant	Hck	Mm_Celera	2:153114292	GTGTGTGCGCTCAAG[C/T]GTGTGTGCACACAGT	15162
rs52162105	snp	C/G			intron-variant	Hck	Mm_Celera	2:153114318	ACAGTAAGGTGAGGA[C/G]GCTAGAGGTTGATGC	15162
rs52230116	snp	G/T			intron-variant	Hck	Mm_Celera	2:153148233	CTCTTTCCATGTCTA[G/T]TAATATACTGTCCTC	15162
rs52280350	snp	A/G			intron-variant	Hck	Mm_Celera	2:153123641	AGGAGGAGGGATGGA[A/G]GGATGGAGGAAGATG	15162
rs52283754	snp	A/G			intron-variant	Hck	Mm_Celera	2:153123633	GGATGGGAAGGAGGA[A/G]GGATGGAGGGATGGA	15162
rs52292429	snp	A/G			intron-variant	Hck	Mm_Celera	2:153123550	GCAACTTGAATGAAC[A/G]AATGAATGAATGAAT	15162
rs52317088	snp	A/G			intron-variant	Hck	Mm_Celera	2:153114301	CTCAAGCGTGTGTGC[A/G]CACAGTAAGGTGAGG	15162
rs52320690	snp	C/G			intron-variant	Hck	Mm_Celera	2:153148153	TGAGTGAGTGAGTGA[C/G]TGAGTGACTGAGTGA	15162
rs52323955	snp	G/T			intron-variant	Hck	Mm_Celera	2:153118503	AACCAGGATATCTCT[G/T]TGGTGGCAGGCTGGC	15162
rs52395784	snp	A/G			intron-variant	Hck	Mm_Celera	2:153123628	AGGAAGGATGGGAAG[A/G]AGGAGGGATGGAGGG	15162
rs52408303	snp	G/T			intron-variant	Hck	Mm_Celera	2:153114576	CTTCTCTCTCCTCTC[G/T]TCTTCCTCTCTCTTC	15162
rs52412265	snp	A/G			intron-variant	Hck	Mm_Celera	2:153123617	GGAGGAAAGGAAGGA[A/G]GGATGGGAAGGAGGA	15162
rs52449311	snp	A/T			intron-variant	Hck	Mm_Celera	2:153130653	TAATTAATATTTTTT[A/T]AATTGACAAATGAGC	15162
rs52486759	snp	A/C			upstream-variant-2KB	Hck	Mm_Celera	2:153108231	TTGGACAGGCTCATT[A/C]CATCATGGGGGGCTT	15162
rs52492443	snp	C/T			intron-variant	Hck	Mm_Celera	2:153114300	GCTCAAGCGTGTGTG[C/T]ACACAGTAAGGTGAG	15162
rs52498091	snp	C/T			intron-variant	Hck	Mm_Celera	2:153114282	GTGTGTGTGTGTGTG[C/T]GCGCTCAAGCGTGTG	15162
rs52519862	snp	G/T			upstream-variant-2KB	Hck	Mm_Celera	2:153108304	CGGGTCAAACCTTGG[G/T]GTCTGAGTAAGTCCT	15162
rs52527681	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153108330	GTCCTTCAAGGACTG[A/G]TTAGCGCCCTTGAGG	15162
rs52565053	snp	C/T			intron-variant	Hck	Mm_Celera	2:153123549	TGCAACTTGAATGAA[C/T]AAATGAATGAATGAA	15162
rs52583144	snp	A/G			intron-variant	Hck	Mm_Celera	2:153135856	CACATGCACACACAC[A/G]TGCACAGAGAGAGAC	15162
rs107704956	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118297	TGCGCCACCACTGCC[C/T]GGCCTCTGGCCACTC	15162
rs107830142	snp	A/G			intron-variant	Hck	Mm_Celera	2:153118344	TTGAAGTCTTATCCA[A/G]AGCAATAAGACAAGA	15162
rs107865732	snp	C/T			intron-variant	Hck	Mm_Celera	2:153150887	TCCCTAACACACACA[C/T]ACACACACACACACA	15162
rs107892664	snp	C/T			intron-variant	Hck	Mm_Celera	2:153120754	AGTTAACATAAAAGC[C/T]GGTTGTAGTAAATGC	15162
rs107953692	snp	C/T			intron-variant	Hck	Mm_Celera	2:153115569	AAAGTCTCCAGAAGG[C/T]GGGGCCCCTTGCCTT	15162
rs108124195	snp	A/G			intron-variant	Hck	Mm_Celera	2:153148689	TCCCCAAAGACCTCT[A/G]GGTCTCCACTTATCA	15162
rs108189168	snp	A/C			intron-variant	Hck	Mm_Celera	2:153111824	TACTGCTGGGACCAT[A/C]GTGTGTGTGTGTGTG	15162
rs108195861	snp	A/G			intron-variant	Hck	Mm_Celera	2:153115099	TTTCTCACAGAAACT[A/G]AAGCTAGACTGCCGG	15162
rs108227325	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118426	GTACATGATCTGTAA[C/T]CTTGGGGTGGTTTGT	15162
rs108329945	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120723	GGAGGAAGGAGGAGG[A/G]AAGACAAAGGATATA	15162
rs108337396	snp	C/T			intron-variant	Hck	Mm_Celera	2:153115098	GTTTCTCACAGAAAC[C/T]AAAGCTAGACTGCCG	15162
rs108378420	snp	C/G			synonymous-codon	Hck	Mm_Celera	2:153151062	CTGGAAGAACCGCCC[C/G]GAGGAACGGCCCACC	15162
rs108380492	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118419	CTGAATAGTACATGA[C/T]CTGTAACCTTGGGGT	15162
rs108403566	snp	A/G			intron-variant	Hck	Mm_Celera	2:153115155	TCTCCCCAAACACCC[A/G]GTTATAGATACGTGC	15162
rs108431384	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118326	TCTTATTCAGTGTAG[C/T]GCTTGAAGTCTTATC	15162
rs108572464	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120721	AGGGAGGAAGGAGGA[A/G]GAAAGACAAAGGATA	15162
rs108716804	snp	A/G			intron-variant	Hck	Mm_Celera	2:153118327	CTTATTCAGTGTAGT[A/G]CTTGAAGTCTTATCC	15162
rs108751707	snp	C/G			intron-variant	Hck	Mm_Celera	2:153115154	ATCTCCCCAAACACC[C/G]AGTTATAGATACGTG	15162
rs108819618	snp	C/G			intron-variant	Hck	Mm_Celera	2:153148173	TGACTGAGTGAGTGA[C/G]TGAGTGAATGAATGC	15162
rs108852727	snp	C/G			intron-variant	Hck	Mm_Celera	2:153148161	TGAGTGACTGAGTGA[C/G]TGAGTGAGTGACTGA	15162
rs108925088	snp	A/C			intron-variant	Hck	Mm_Celera	2:153115111	ACTAAAGCTAGACTG[A/C]CGGCCAGCATGCCCC	15162
rs211736219	snp	C/T			intron-variant	Hck	Mm_Celera	2:153150515	ATAAATACAAACAAA[C/T]GGATAGATAGATAAA	15162
rs211794671	in-del	-/A			intron-variant	Hck	Mm_Celera	2:153127449	AAAACAAAACAGAAC[-/A]AAAAAAACAAGCATC	15162
rs211846477	snp	C/G			intron-variant	Hck	Mm_Celera	2:153149890	ACATGGGTACCTGGG[C/G]CAGGTGGTAGCACAT	15162
rs211933912	snp	A/G			intron-variant	Hck	Mm_Celera	2:153113224	ACGGGATGCAGCACA[A/G]GGCCGATTCAGAGGA	15162
rs212014594	snp	A/G			intron-variant	Hck	Mm_Celera	2:153112256	TGTTAGTATTTCCCC[A/G]TGTCATTAAGATTGC	15162
rs212027383	snp	C/T			intron-variant	Hck	Mm_Celera	2:153119741	TCACTCTGTACAAAA[C/T]CAACTCGGCCTTCAT	15162
rs212242358	snp	A/C			intron-variant	Hck	Mm_Celera	2:153128524	CAGTCTGTGGGTCAC[A/C]GTCTGTCACTGAGGG	15162
rs212374602	in-del	-/AA			intron-variant	Hck	Mm_Celera	2:153128724	TAACCATCAATCTAG[-/AA]AAAAAAAAAAAAAAT	15162
rs212382942	snp	C/T			intron-variant	Hck	Mm_Celera	2:153121132	GCCTGACAACCTGTT[C/T]GGATCCACAGAACTA	15162
rs212410271	snp	C/T			intron-variant	Hck	GRCm38.p3	2:153136605	ACCGGTGTCCAGGCC[C/T]CTCTCTCTGTCTTAA	15162
rs212509978	snp	A/G			intron-variant	Hck	Mm_Celera	2:153118166	TTGATTTGGTTTTTC[A/G]AGACAGGGTTTCTCT	15162
rs212582189	in-del	-/GGCTGCTCTGATGACATTACTA			intron-variant	Hck	Mm_Celera	2:153142419	CTGAGCAAGGCGCTT[-/GGCTGCTCTGATGACATTACTA]GCCACCTCTCAAGTG	15162
rs212631034	snp	A/G			intron-variant	Hck	Mm_Celera	2:153124726	ATCCTGCCTCAATAT[A/G]TAAGACTGAAAGTAA	15162
rs212640810	snp	C/T			intron-variant	Hck	Mm_Celera	2:153129165	CTAGCCTGGTCCCCC[C/T]TGAGACACACCCACC	15162
rs212646205	in-del	-/AAAG			intron-variant	Hck	GRCm38.p3	2:153140957	CTTAAAAAAAAAAAA[-/AAAG]AAAGAAAGAAAAAAG	15162
rs212659943	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153144354	GCAGATGTCTTCCAG[-/T]TTTTTAAGAGCAGAT	15162
rs212767723	in-del	-/C			intron-variant	Hck	Mm_Celera	2:153144313	CCAGGATCCTTCTGA[-/C]CCCCCCCCCCAAATG	15162
rs212851807	in-del	-/T			upstream-variant-2KB	Hck	Mm_Celera	2:153106624	GTTATATCCTTCTAA[-/T]TTCCCCCTGGGCCTG	15162
rs212856638	snp	A/G			intron-variant	Hck	Mm_Celera	2:153110242	CATCTAAGAGCACTC[A/G]CTGCTCTTTCCAAGG	15162
rs212865572	snp	A/T			intron-variant	Hck	Mm_Celera	2:153135064	ATTCATAGTGAGGGG[A/T]AAGGCTTGGGTTTTC	15162
rs213032775	snp	A/C			intron-variant	Hck	Mm_Celera	2:153141804	GAGGGCCAGGGTTCA[A/C]TTCCCAGCACCCACA	15162
rs213192862	snp	C/G			intron-variant	Hck	Mm_Celera	2:153149230	CTCCACCATCCCTCC[C/G]CTAGTGTAAGGGGTT	15162
rs213206095	snp	A/G			intron-variant	Hck	Mm_Celera	2:153110906	AAGTAAAATGACTAG[A/G]TGTAATGGGTAAAAT	15162
rs213311100	snp	C/G			intron-variant	Hck	Mm_Celera	2:153111037	AATGTGTCCTCTGTG[C/G]TGTAAAGATTATAGC	15162
rs213345299	in-del	-/TCT			intron-variant	Hck	Mm_Celera	2:153114354	ATATTCTTTGATTGC[-/TCT]TCTTCTTATTCACTG	15162
rs213351000	snp	A/G			intron-variant	Hck	Mm_Celera	2:153112076	TCTCTGCTGTGACAA[A/G]CGTCAGTTGCCTGTT	15162
rs213568819	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118188	GGTTTCTCTGTGTAG[C/T]CCTGGCTGTCCTGGA	15162
rs213661322	snp	A/G			intron-variant	Hck	Mm_Celera	2:153125857	CTTATAATCACAGCA[A/G]TGGAGAGGCAGAGGC	15162
rs213835668	snp	G/T			intron-variant	Hck	Mm_Celera	2:153135794	CACACTGAAAAGAGG[G/T]AACTGCTGGAAAAGA	15162
rs213908504	snp	C/T			intron-variant	Hck	Mm_Celera	2:153141833	CATGGTAGCTCACAG[C/T]TGTCTGTAACTCCAG	15162
rs213944450	snp	C/T			intron-variant	Hck	Mm_Celera	2:153142769	GACCCTAACCCTCCC[C/T]GAGCCCATAGTTTGA	15162
rs213944704	snp	A/C			intron-variant	Hck	Mm_Celera	2:153135199	CCCTGTGGTCCTTGG[A/C]CCAGTACCTTGAGAA	15162
rs214195579	snp	A/G			intron-variant	Hck	Mm_Celera	2:153133172	GAAGCCAAGAGTCTG[A/G]GTTTGCTGGTCTCTG	15162
rs214263295	snp	G/T			intron-variant	Hck	Mm_Celera	2:153149246	CTAGTGTAAGGGGTT[G/T]GCTGGCTATCTCCTC	15162
rs214266860	snp	C/T			intron-variant	Hck	Mm_Celera	2:153145107	TTCACCCCCATCACA[C/T]CACACACCAATGCCA	15162
rs214308285	snp	A/G			intron-variant	Hck	Mm_Celera	2:153138410	TTCTCTGTGTCTTTC[A/G]TGTGAATACTCATGC	15162
rs214409879	in-del	-/CTCTCTCTCTCTCTCTCTCTCT			intron-variant	Hck	Mm_Celera	2:153118115	TTCCTCCCAAGTCAG[-/CTCTCTCTCTCTCTCTCTCTCT]CTCTCTCTCTCTCTT	15162
rs214426032	snp	A/G			intron-variant	Hck	Mm_Celera	2:153126769	TGGAAGGAGAGAAAC[A/G]AGTCTACCGGTCCCT	15162
rs214470326	snp	C/T			intron-variant	Hck	Mm_Celera	2:153139817	AAAGGCCCACCACCT[C/T]CCCCCAGGGCCCTGG	15162
rs214506169	snp	G/T			intron-variant	Hck	Mm_Celera	2:153140443	AGGGGCTCAGATCCC[G/T]GGGAAGTCTAAGCAG	15162
rs214521181	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130522	CCTTCTGGCTTCCCT[A/G]GGTACCAGCTCACAC	15162
rs214595095	snp	A/G			intron-variant	Hck	Mm_Celera	2:153148666	TCAAGCCCCCCGGAG[A/G]TCACTTATCCCCAAA	15162
rs214687066	snp	A/C			intron-variant	Hck	Mm_Celera	2:153109413	CTCTCTGGATTCCAG[A/C]TTCCAACTCTGTAAA	15162
rs214703250	snp	C/T			intron-variant	Hck	Mm_Celera	2:153131120	AGGTGTTTGGGCCCC[C/T]GATCTGAGTGGGCTG	15162
rs214803202	snp	C/T			intron-variant	Hck	Mm_Celera	2:153123459	CTAAGAGATATAAAC[C/T]TTCTGGAAAGTATTG	15162
rs214992906	in-del	-/AA			intron-variant	Hck	Mm_Celera	2:153109679	TGAAAATTAGGTCTT[-/AA]AGAGACATTTGTGTA	15162
rs215021879	snp	C/T			intron-variant	Hck	Mm_Celera	2:153138904	CTAGAGCTATAGTTA[C/T]AGGTGCTTGTGAGCC	15162
rs215103282	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153107775	GTAGTACAAACTACG[A/G]AGAGAGAGGCCCTGG	15162
rs215104628	snp	A/G			intron-variant	Hck	Mm_Celera	2:153139701	GCAGGGCTGATTAGA[A/G]GGAGGGGGTGGCTCC	15162
rs215215624	snp	C/T			intron-variant	Hck	Mm_Celera	2:153133298	ACAAGTGCTGCTTGG[C/T]TCATGGCTGTTCCTC	15162
rs215242041	in-del	-/C			intron-variant	Hck	Mm_Celera	2:153143522	CCCACCTCTGCTTAG[-/C]TACCTGGCTCTATGT	15162
rs215727944	snp	A/G			intron-variant	Hck	Mm_Celera	2:153131373	CAAGGCGCCTCTCCA[A/G]CCTTAGGGAAGTCCT	15162
rs215887959	snp	A/G			intron-variant	Hck	Mm_Celera	2:153113351	GAGCAGATACAGAGA[A/G]ATCTCCATGGCACAG	15162
rs215958612	snp	C/T			intron-variant	Hck	Mm_Celera	2:153148306	TAGCCAAGAGATCAC[C/T]AGAAGAAACAAAAAA	15162
rs215959425	snp	A/C			upstream-variant-2KB	Hck	Mm_Celera	2:153107813	TCTCTAGAACACACA[A/C]GCGCGCGCGCGCGCG	15162
rs215997512	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153108462	GTATTTGGGGGCGGG[A/G]TTTGCATCACCCAGG	15162
rs216017077	in-del	-/C			intron-variant	Hck	Mm_Celera	2:153132675	CAGGTACACCAGGTT[-/C]CCCCTTGACTGGGAT	15162
rs216143532	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130261	ACACCTGCGCTCTGG[A/G]GTTAGACTGCCTAGG	15162
rs216157688	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153150209	CCCTAATCACAGAAG[-/T]TTTAAAAAATACTAA	15162
rs216316109	in-del	-/T			intron-variant	Hck	GRCm38.p3	2:153136235	GTTTCAAGGCAGCGT[-/T]TAAGCTTACATGCTA	15162
rs216327538	snp	C/T			intron-variant	Hck	Mm_Celera	2:153129678	AGACTGTGGTTTCAG[C/T]CCAGACTCCTGTGGC	15162
rs216372955	snp	A/T			intron-variant	Hck	Mm_Celera	2:153150665	CAGGCGAATCTCTTC[A/T]GTTTGAATTTGAGGC	15162
rs216407811	snp	C/T			intron-variant	Hck	GRCm38.p3	2:153140531	TTGCATCTCAGTGGG[C/T]CGGGTCTTCTGGGAA	15162
rs216565828	snp	A/C			downstream-variant-500B	Hck	Mm_Celera	2:153151695	CAGAGGATGTCCAGA[A/C]AGTCTGGCCTAATTG	15162
rs216676789	snp	A/C			intron-variant	Hck	Mm_Celera	2:153150869	AGCTCCATTTGCTAC[A/C]CCTCCCTAACACACA	15162
rs216737026	snp	C/G			intron-variant	Hck	Mm_Celera	2:153145848	TGCCTCAGAATAGCT[C/G]GAAGGAGCCTTCTGA	15162
rs216755187	in-del	-/AA			intron-variant	Hck	Mm_Celera	2:153145688	AGAAACCCTGTCTTT[-/AA]AAAAAAAAAATCATT	15162
rs216768527	snp	A/G			intron-variant	Hck	Mm_Celera	2:153146694	TAAAAGAAAAGGAGT[A/G]GCAAATTGGCTGAGT	15162
rs216769807	snp	C/T			intron-variant	Hck	Mm_Celera	2:153144176	AAACATTCACATTGC[C/T]TGTTCCTTAAGAACA	15162
rs216786177	in-del	-/CA			intron-variant	Hck	Mm_Celera	2:153113168	AATGCTCACAATACG[-/CA]CACACACACACATCA	15162
rs216826175	snp	A/G			intron-variant	Hck	Mm_Celera	2:153145204	AAGGTTCTACATCAT[A/G]GAATTCAAAACCAGG	15162
rs216896417	snp	A/G			intron-variant	Hck	Mm_Celera	2:153123344	GTTCTAGCCCCTCAG[A/G]CCCCAGAACTGCTGT	15162
rs216906528	snp	C/G			downstream-variant-500B	Hck	Mm_Celera	2:153151550	CAAGCGAGAATCCAG[C/G]TGGGGAGATGGCTCT	15162
rs217105801	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120973	GTCTCTAACAATGGA[A/G]TCTCTCTATGTGTGG	15162
rs217206874	in-del	-/AAAAAAAAA			intron-variant	Hck	Mm_Celera	2:153139606	GCAGAGTGTGTCATT[-/AAAAAAAAA]AAAAAAAAAAAAAAA	15162
rs217289735	snp	A/G			intron-variant	Hck	Mm_Celera	2:153125886	GCAAGCAGATTCCTG[A/G]GGCATGCTGTGAGAC	15162
rs217346212	snp	A/C			intron-variant	Hck	Mm_Celera	2:153129341	ACAGGCTCTCCACAA[A/C]GCCTTCCTAAGGGAT	15162
rs217365740	snp	C/T			intron-variant	Hck	Mm_Celera	2:153115601	GGGTGACCCAGGGCC[C/T]ACTGTGGGTCTCTGG	15162
rs217454289	in-del	-/CCCC			intron-variant	Hck	Mm_Celera	2:153122167	CCATGAGACAAAGCA[-/CCCC]CCCCCCATTCAGGCT	15162
rs217512858	snp	C/G			intron-variant	Hck	Mm_Celera	2:153135877	AGAGAGAGACAGAGA[C/G]ACAGAGACAGAGTAA	15162
rs217572116	snp	A/C			intron-variant	Hck	Mm_Celera	2:153128446	ACTTGGCTTTTGTGA[A/C]GTTGTGATTAATACA	15162
rs217654714	snp	A/G			intron-variant	Hck	Mm_Celera	2:153138106	GAGGAGGAGGTGGTT[A/G]GCTGGAGATGTAACT	15162
rs217666891	in-del	-/TGACAT			intron-variant	Hck	Mm_Celera	2:153110185	CCTTACTTTTGAAGG[-/TGACAT]TAAACTGAAGGAAAG	15162
rs217727730	snp	A/G			intron-variant	Hck	Mm_Celera	2:153128004	TTCAGACATCTCTAA[A/G]CAACACAGATCTGGA	15162
rs217740737	snp	A/G			intron-variant	Hck	Mm_Celera	2:153149355	AGCATGAGGCTGAGA[A/G]GAAGTCAACTTTTTT	15162
rs217766491	snp	C/T			intron-variant	Hck	Mm_Celera	2:153142336	CACATCAGCTTATTA[C/T]CATCAGGTCCCAGGG	15162
rs217816767	in-del	-/AA/AAAA			intron-variant	Hck	Mm_Celera	2:153144321	TTCTGACCCCCCCCC[-/AA/AAAA]CCAAATGCAGGGCTG	15162
rs217894827	snp	C/T			intron-variant	Hck	Mm_Celera	2:153144357	GATGTCTTCCAGTTT[C/T]TTAAGAGCAGATTCT	15162
rs217912561	in-del	-/CACAGGCGAGA			intron-variant	Hck	Mm_Celera	2:153119793	AAAGCACAGGCGAGG[-/CACAGGCGAGA]TTTTCCTGCAAAGGA	15162
rs218073605	snp	A/G			intron-variant	Hck	Mm_Celera	2:153114906	CCAGCCTTGTGTAAA[A/G]GGGACAGTCAGCTCC	15162
rs218192714	snp	A/G			intron-variant	Hck	Mm_Celera	2:153138997	TGAGCCATCTCTCCA[A/G]ATTCTGGAATAATTT	15162
rs218201725	snp	A/C			intron-variant	Hck	Mm_Celera	2:153143381	CACACTGTCTTGGAG[A/C]CACAGTGGTCCTTAA	15162
rs218302688	snp	C/T			intron-variant	Hck	Mm_Celera	2:153114320	AGTAAGGTGAGGACG[C/T]TAGAGGTTGATGCTG	15162
rs218314915	snp	A/C			utr-variant-5-prime	Hck	Mm_Celera	2:153108632	ACGCAGCCTCTGTAG[A/C]CCGCAAGTCTTCGTC	15162
rs218346541	snp	A/T			intron-variant	Hck	Mm_Celera	2:153150171	TTCTTGTTTTTGCTC[A/T]TAATCACTGACCCAT	15162
rs218355270	snp	C/T			intron-variant	Hck	Mm_Celera	2:153120499	AAAGTGAGATACATA[C/T]ACAGAATGGAGTATT	15162
rs218363951	snp	A/G			intron-variant	Hck	Mm_Celera	2:153112645	TTGAGGGTACAGTCT[A/G]TCAGGGTGGAGCAGG	15162
rs218425850	snp	A/T			upstream-variant-2KB	Hck	Mm_Celera	2:153107857	AACCCTTTCAGAAAA[A/T]TTGATTACAAATCTA	15162
rs218441057	snp	A/G			intron-variant	Hck	Mm_Celera	2:153113594	AGATTCACTTAGGAT[A/G]TTTATACTTTTAACA	15162
rs218447202	snp	A/G			intron-variant	Hck	Mm_Celera	2:153140544	GGTCGGGTCTTCTGG[A/G]AAACAATGGTCTGGC	15162
rs218453222	snp	A/G			intron-variant	Hck	Mm_Celera	2:153116427	TTGGCAACTCCACAT[A/G]ACTCTAACTTCAGGC	15162
rs218501276	snp	A/G			intron-variant	Hck	Mm_Celera	2:153119922	ATAATGACAATATTA[A/G]AAACTGCAAGAGCTA	15162
rs218557431	snp	C/T			intron-variant	Hck	Mm_Celera	2:153146534	CTGGCACTCATATGT[C/T]GGCTCCCAATCATCT	15162
rs218743650	snp	A/G			intron-variant	Hck	Mm_Celera	2:153142077	AAATAAATTATATTT[A/G]GAGAGAGAGGGGAAG	15162
rs218775963	snp	A/G			intron-variant	Hck	Mm_Celera	2:153149782	ATAAAATACAAATAA[A/G]TAAATAAATCTGAGG	15162
rs218861793	snp	A/G			intron-variant	Hck	Mm_Celera	2:153112229	TTTTTGTTCTACTTC[A/G]CTTAATTAAGCTGTT	15162
rs218864715	snp	C/T			intron-variant	Hck	GRCm38.p3	2:153131376	GGCGCCTCTCCAACC[C/T]TAGGGAAGTCCTCTG	15162
rs218933640	snp	A/C			intron-variant	Hck	Mm_Celera	2:153124465	CAAATGAGTGTGTTC[A/C]TTGTGTTCCTTCAGC	15162
rs219012321	snp	A/C			intron-variant	Hck	Mm_Celera	2:153119688	TGTTGATAAACTGTG[A/C]GTGCACGTGTAAAAG	15162
rs219046286	in-del	-/A			intron-variant	Hck	Mm_Celera	2:153137967	ATCACAGAACTTGAG[-/A]GGCAGAGGCAGGCAG	15162
rs219167214	snp	A/T			intron-variant	Hck	Mm_Celera	2:153147088	GTGTGTGTGTGTGAG[A/T]GAGATGTGGATATTT	15162
rs219287732	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120408	CAGCTGCACAGCCTC[A/G]TTTATTGCTGCACTA	15162
rs219354862	snp	C/T			intron-variant	Hck	Mm_Celera	2:153110536	TCTTTCCACTGTTCC[C/T]GTCCAGCCCGAGAGA	15162
rs219378227	snp	A/T			intron-variant	Hck	Mm_Celera	2:153147127	GTTGAGACTTGTCAA[A/T]ACTTAATCACTTACT	15162
rs219403534	snp	C/T			intron-variant	Hck	Mm_Celera	2:153111568	CGGTTCACTCTGGGC[C/T]TGAAACTGCAACCTC	15162
rs219431147	snp	A/G			intron-variant	Hck	Mm_Celera	2:153144224	GAAGTTTGATGTTCT[A/G]AAAGAGCCCACAAGC	15162
rs219477564	snp	C/T			intron-variant	Hck	Mm_Celera	2:153112391	GTTATAAGTGTCTGT[C/T]TATACATATGTGTGT	15162
rs219496156	snp	A/G			intron-variant	Hck	Mm_Celera	2:153109588	CCCTATCCAAACTAC[A/G]CCTGATCAGAGGGGT	15162
rs219564097	snp	A/T			intron-variant	Hck	Mm_Celera	2:153116883	GGTTCACAGAGGAGA[A/T]CTGGGGAGCTGCTGC	15162
rs219626084	in-del	-/ACACACACACACACACACACAC			intron-variant	Hck	Mm_Celera	2:153146092	ACTCAGTCTCCAGTA[-/ACACACACACACACACACACAC]ACACACACACACACA	15162
rs219737355	snp	A/T			intron-variant	Hck	Mm_Celera	2:153122849	CGATGTACTGTGTTC[A/T]GGGGCTATGGTCATA	15162
rs219818115	snp	A/C			intron-variant	Hck	Mm_Celera	2:153134808	AGAGTCCATAAAGCC[A/C]GAGCTGGGAGGGCCC	15162
rs219860974	snp	C/G			intron-variant	Hck	Mm_Celera	2:153140689	ACTGACTGCTCTTTT[C/G]AAGGTACTGAGTTCA	15162
rs219863845	in-del	-/AA			intron-variant	Hck	Mm_Celera	2:153124867	ATATGCATGCAAAAC[-/AA]AAAAAATCAATAGTG	15162
rs219911291	snp	A/C			intron-variant	Hck	Mm_Celera	2:153110452	ACACACACACACACA[A/C]AATCTGAAAGAGGGG	15162
rs219983328	snp	C/T			intron-variant	Hck	Mm_Celera	2:153127059	TGTCCCACAAGTCCT[C/T]AGTCTCTAAATTGTG	15162
rs220104006	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153130180	AAAAAGGGACGTTGC[-/T]TTTTTTTTTTTAAAT	15162
rs220159173	snp	G/T			intron-variant	Hck	Mm_Celera	2:153146023	TCTCAAAATAAAAAG[G/T]AAAGGGGCTGTGGTT	15162
rs220194006	snp	A/C			intron-variant	Hck	Mm_Celera	2:153139093	TTTGAGCTACGTCAC[A/C]ATCCATGTAAGTCAT	15162
rs220228517	snp	A/C			intron-variant	Hck	Mm_Celera	2:153143888	GGGCTGGAGAGTTGG[A/C]TCAGAGGTTAAGAGC	15162
rs220257529	snp	C/G			intron-variant	Hck	Mm_Celera	2:153145367	GTGACAGAACAGAGA[C/G]AACTGTTGGAAACCC	15162
rs220283392	in-del	-/CTGGTATC			intron-variant	Hck	Mm_Celera	2:153127187	AAACTTCTCACACTG[-/CTGGTATC]CTGATCTGGGTAGTG	15162
rs220466640	in-del	-/GGTG			intron-variant	Hck	Mm_Celera	2:153120156	AGGCAGGGGAACTGT[-/GGTG]AGTGAGTTTTAGGCT	15162
rs220571045	snp	C/T			intron-variant	Hck	Mm_Celera	2:153128091	AGGGTCCCGATCACA[C/T]TTTAAGATAGCTCTA	15162
rs220768807	snp	A/G			intron-variant	Hck	Mm_Celera	2:153109031	GAATGGCAGTGCTGA[A/G]CTGAGGCTTCTCTGT	15162
rs220868520	snp	C/T			intron-variant	Hck	Mm_Celera	2:153130702	TCTTTAATTCCAACA[C/T]TTGGAAGGCAGAGGC	15162
rs220935837	snp	A/G			intron-variant	Hck	Mm_Celera	2:153132540	ACCTGTGGACAGGAA[A/G]GTGGCCTGGACTCGC	15162
rs220979981	in-del	-/CG			intron-variant	Hck	Mm_Celera	2:153110277	TAGCTAAGTTCTCAC[-/CG]ATCGCTCACAACAAC	15162
rs221008179	snp	A/G			intron-variant	Hck	Mm_Celera	2:153109504	GGTACTGGAGAGAGA[A/G]CCTGGTTTGTCTGTG	15162
rs221016292	snp	A/T			intron-variant	Hck	Mm_Celera	2:153138513	AAATAGTATATTTAC[A/T]GTAAATATACTATTT	15162
rs221261704	snp	A/G			intron-variant	Hck	Mm_Celera	2:153116185	CAGTGCCACCAGCTT[A/G]ACAAGATCCACAGTC	15162
rs221353974	snp	C/T			intron-variant	Hck	Mm_Celera	2:153142414	CGGCTCTGAGCAAGG[C/T]GCTTGGCTGCTCTGA	15162
rs221374362	snp	G/T			intron-variant	Hck	Mm_Celera	2:153135527	CAAACACCACAGATC[G/T]GGATTTGAGCTTCCT	15162
rs221405168	snp	A/G			intron-variant	Hck	Mm_Celera	2:153132611	CCTGATTTAGAACAC[A/G]GTCCCAAGCACTTGG	15162
rs221480798	in-del	-/GCACGCACACTA			intron-variant	Hck	Mm_Celera	2:153110452	CACACACACACACAC[-/GCACGCACACTA]AATCTGAAAGAGGGG	15162
rs221726249	snp	A/G			intron-variant	Hck	Mm_Celera	2:153121208	GGAAGAATGGGAGGT[A/G]GAGGCAGGAGAATGA	15162
rs221782293	snp	C/G			intron-variant	Hck	Mm_Celera	2:153121810	AGTTGTCCTCTGAAA[C/G]CCCTGCATGCAAGCC	15162
rs221830828	snp	A/C			intron-variant	Hck	Mm_Celera	2:153128684	ATGGTTCCTAGTGGG[A/C]CAGCCAACCACCAAT	15162
rs221867487	in-del	-/AAAAAAAG			intron-variant	Hck	GRCm38.p3	2:153140953	AAATCTTAAAAAAAA[-/AAAAAAAG]AAAGAAAGAAAAAAG	15162
rs221894197	in-del	-/AA			upstream-variant-2KB	Hck	Mm_Celera	2:153107812	TTCTCTAGAACACAC[-/AA]GCGCGCGCGCGCGCG	15162
rs221897577	snp	A/G			intron-variant	Hck	Mm_Celera	2:153128232	TCCTCACAATTTCAG[A/G]CTCATGTCCTTTTCC	15162
rs221947301	snp	C/G			intron-variant	Hck	GRCm38.p3	2:153133683	ATACATAGATACATA[C/G]ATACATAGATGAATA	15162
rs221963943	snp	C/T			intron-variant	Hck	Mm_Celera	2:153140590	AAGCATGTAAGCAGC[C/T]GGAGCTTTGCTGGTG	15162
rs221980679	snp	G/T			intron-variant	Hck	Mm_Celera	2:153137809	TTAACTAGCACTGCA[G/T]CTGGGCGGGGATAAA	15162
rs222029728	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153107309	GTTTCTGCAGGTGTG[C/T]GTTGCAGTTTAGAGA	15162
rs222208943	snp	A/G			intron-variant	Hck	Mm_Celera	2:153113705	TGGGTGGAACCAGAG[A/G]GCAGCTTGTGAGAAT	15162
rs222252544	snp	C/T			intron-variant	Hck	Mm_Celera	2:153147813	TTTGAAATGGAACTG[C/T]TTGCAGCCTTCTAGC	15162
rs222565901	snp	C/T			intron-variant	Hck	Mm_Celera	2:153124295	GCAAGCTGGTGAGTA[C/T]GGCATCCCAGGGAGC	15162
rs222660646	in-del	-/G			intron-variant	Hck	GRCm38.p3	2:153149879	CAGGTGGTGGCACAT[-/G]GGTACCTGGGGCAGG	15162
rs222758037	snp	A/T			intron-variant	Hck	Mm_Celera	2:153118956	TGCTAAGTTACCAAA[A/T]GCAATCTGCAGTTTC	15162
rs222838677	in-del	-/C			intron-variant	Hck	Mm_Celera	2:153149884	GGTGGCACATGGGTA[-/C]CTGGGGCAGGTGGTA	15162
rs223024732	snp	A/G			intron-variant	Hck	Mm_Celera	2:153129769	AAGGAGAGCTTCTAG[A/G]CCCAGGTGGGGGGCC	15162
rs223076152	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153107543	GGTGGAGGGAAAACC[A/G]CTGCATGTGGGAGGG	15162
rs223201407	snp	A/G			intron-variant	Hck	Mm_Celera	2:153134617	CTGACTGGGCACTCT[A/G]TTTCAGAGGGGAAGG	15162
rs223236636	snp	A/G			intron-variant	Hck	Mm_Celera	2:153128773	CAGTCAATCTGATTG[A/G]CCTACTCTATCTTTG	15162
rs223257916	snp	C/T			intron-variant	Hck	Mm_Celera	2:153123716	TTCATTGTTGGGACA[C/T]ATGATGACAGTGTAG	15162
rs223426523	snp	C/T			intron-variant	Hck	Mm_Celera	2:153109631	AGTGTGGCAGAATTC[C/T]GTATGTCAAGTGCAC	15162
rs223492381	in-del	-/GCAGGTGCCCCGTCC			intron-variant	Hck	GRCm38.p3	2:153148866	TATTTGTAGAGGGCA[-/GCAGGTGCCCCGTCC]TGATTCCCCTCACCC	15162
rs223513691	snp	A/G			intron-variant	Hck	Mm_Celera	2:153149577	CTTGAGGCTGGAGAG[A/G]TGGATCAGAGGTTAA	15162
rs223562453	in-del	-/GC			upstream-variant-2KB	Hck	Mm_Celera	2:153107813	CTCTAGAACACACAA[-/GC]GCGCGCGCGCGCGCG	15162
rs223677761	snp	G/T			intron-variant	Hck	Mm_Celera	2:153126839	ACACTTACACATCAT[G/T]CACTCACAGAATAAA	15162
rs223888271	snp	G/T			intron-variant	Hck	Mm_Celera	2:153116015	CCTTCCCACAGGAAT[G/T]TATTTCTTCTTTGGG	15162
rs223907364	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118724	AAATCAGTAGATTTT[C/T]TATATCTGAATAATG	15162
rs223938182	snp	C/T			intron-variant	Hck	Mm_Celera	2:153119479	AGGGAACCAATGGTG[C/T]CTAGTTTTGTTTTTT	15162
rs224039092	snp	A/T			intron-variant	Hck	Mm_Celera	2:153122228	TGGACATTCATGCTG[A/T]CCTGGGTTCCATTCA	15162
rs224340167	snp	C/G			intron-variant	Hck	Mm_Celera	2:153117464	CCCCACTACACAGGG[C/G]GGGGGGTGAACTAGG	15162
rs224343496	snp	C/G			intron-variant	Hck	Mm_Celera	2:153149637	CCAGTTCCTAGCACC[C/G]ATGTGGTAACTCACA	15162
rs224345949	snp	C/G			intron-variant	Hck	Mm_Celera	2:153141812	GGGTTCAATTCCCAG[C/G]ACCCACATGGTAGCT	15162
rs224388589	in-del	-/G			intron-variant	Hck	Mm_Celera	2:153147474	TAAGAGAGTAGCACA[-/G]GGGGAAAGCCTCCAT	15162
rs224420063	in-del	-/AG			intron-variant	Hck	Mm_Celera	2:153125556	AGACAGAGAGAGGAA[-/AG]AGAGAGAAAGAGAAA	15162
rs224456779	snp	C/T			intron-variant	Hck	Mm_Celera	2:153146930	TGTGCTGGTTTTGTG[C/T]AGGCAGACATAGCTT	15162
rs224488006	snp	A/G			intron-variant	Hck	Mm_Celera	2:153149234	ACCATCCCTCCGCTA[A/G]TGTAAGGGGTTGGCT	15162
rs224496257	snp	G/T			intron-variant	Hck	Mm_Celera	2:153139885	GGGGCTATGTAAGCC[G/T]CTGGGACACATCTTA	15162
rs224673267	snp	A/G			intron-variant	Hck	Mm_Celera	2:153146314	CATGCTCAAGATCTG[A/G]GTTTGAGCCTTAGTA	15162
rs224703891	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120711	GGAGGCCTAGAGGGA[A/G]GAAGGAGGAGGAAAG	15162
rs224745089	snp	G/T			intron-variant	Hck	Mm_Celera	2:153117126	GATCTACAGCCAGCA[G/T]GACAGCCCTGGGAAA	15162
rs224799017	snp	A/G			intron-variant	Hck	Mm_Celera	2:153145510	CTGAGCGCCAGGGAT[A/G]GGGCTGGATAACATG	15162
rs224822332	snp	C/G			intron-variant	Hck	Mm_Celera	2:153128585	GTTAGCTAGAGACAG[C/G]AACTGAAGCAGAGAA	15162
rs224849802	in-del	-/TCC			intron-variant	Hck	Mm_Celera	2:153123277	ACAGGTGAATGTGTT[-/TCC]TCTTAAGTTAATACA	15162
rs224961170	snp	A/G			intron-variant	Hck	Mm_Celera	2:153149534	ACAGCATCACACCTG[A/G]ATGATCTCTACTTTT	15162
rs224978919	in-del	-/GGCA			intron-variant	Hck	Mm_Celera	2:153131928	GGAAGCTCTTTTGTG[-/GGCA]GGCATGTGGATGGGA	15162
rs225042491	snp	C/G			intron-variant	Hck	Mm_Celera	2:153149944	ACATGGGTACCTGGG[C/G]CAGGTGTTGGCACAT	15162
rs225065272	in-del	-/GGA			intron-variant	Hck	Mm_Celera	2:153120689	GTGTGTGTGAGGGAG[-/GGA]GGAGGAGGAGGCCTA	15162
rs225145983	in-del	-/CCAGAACT			intron-variant	Hck	Mm_Celera	2:153126743	GCCTGAGTTAAGACC[-/CCAGAACT]CACATAAAGATGGAA	15162
rs225425123	snp	C/T			downstream-variant-500B	Hck	Mm_Celera	2:153151828	GTGCACATAAACCTG[C/T]ATACACACATATACC	15162
rs225429823	snp	C/T			intron-variant	Hck	Mm_Celera	2:153140081	CTCCTGCTCTCTGCT[C/T]TCTGGGGGGAAACCT	15162
rs225451587	in-del	-/TC			intron-variant	Hck	Mm_Celera	2:153112359	TGGTTTTTCAACTTT[-/TC]TTTTTTATAATGTGT	15162
rs225508093	snp	C/T			intron-variant	Hck	Mm_Celera	2:153138822	ATATGGGTCTTTTGC[C/T]TGTCTATGAGTCTGT	15162
rs225509414	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153149170	ACTCAGCTCTTGATC[-/T]TTCCCCCAGTCCCTC	15162
rs225514266	snp	A/G			intron-variant	Hck	Mm_Celera	2:153110800	AGGGTGCTGTTTAGT[A/G]GAATATGTGCCCATG	15162
rs225551884	snp	C/T			intron-variant	Hck	Mm_Celera	2:153117895	TCACAAATCAGTACA[C/T]GTAACATAGATAGTA	15162
rs225561369	in-del	-/AACAACAACAA			intron-variant	Hck	Mm_Celera	2:153127448	AAAACAAAACAGAAC[-/AACAACAACAA]AAAAAAAACAAGCAT	15162
rs225594009	snp	G/T			intron-variant	Hck	Mm_Celera	2:153109188	GGTAGACAGCAGCCA[G/T]GGCTAAAGGAACAGC	15162
rs225620294	snp	C/T			intron-variant	Hck	Mm_Celera	2:153145623	CACTGCATTCAAAGC[C/T]AGTCTGGTCTGCAGG	15162
rs225632509	snp	A/G			intron-variant	Hck	Mm_Celera	2:153109969	CACTTTACCAACTGG[A/G]CTATCTTCCTGGCCC	15162
rs225676614	snp	A/C			intron-variant	Hck	Mm_Celera	2:153121189	TGTTTAATCCACCAT[A/C]CGTGGAAGAATGGGA	15162
rs225716192	in-del	-/G			intron-variant	Hck	Mm_Celera	2:153125175	TAAGCCTCCCAAACT[-/G]GGGCCGTCAGTTTGG	15162
rs225778480	in-del	-/CCCAGCAGGGCCTATAAT			intron-variant	Hck	Mm_Celera	2:153124651	GCCAGAGTTTGAATC[-/CCCAGCAGGGCCTATAAT]CCCAGCACACAGAGG	15162
rs225787616	in-del	-/AGAGAC			intron-variant	Hck	Mm_Celera	2:153135874	CACAGAGAGAGACAG[-/AGAGAC]AGAGACAGAGTAATT	15162
rs225873652	in-del	-/AGAGCCCACAAGC			intron-variant	Hck	Mm_Celera	2:153144227	GTTTGATGTTCTAAA[-/AGAGCCCACAAGC]AGAGCCAGGACTTGA	15162
rs225955717	snp	A/G			intron-variant	Hck	Mm_Celera	2:153137836	TAAATGCTGGGAGTC[A/G]AGACTAATCTACTAG	15162
rs225991685	snp	A/G			intron-variant	Hck	Mm_Celera	2:153113875	TACAGAACTGTCCCC[A/G]TGAAACCCGTTGTTT	15162
rs225992541	in-del	-/C			intron-variant	Hck	Mm_Celera	2:153118397	GAAGAAGTCAGATCA[-/C]CCCCATCTGAATAGT	15162
rs226087362	snp	C/T			intron-variant	Hck	Mm_Celera	2:153136938	TCTCCAAGATGGCCT[C/T]GGCGTGGCTCTTCTG	15162
rs226261420	snp	A/C			intron-variant	Hck	Mm_Celera	2:153138556	TTCCCCTGCATGCTA[A/C]TTAAAGCATCTCTAG	15162
rs226300497	snp	C/T			intron-variant	Hck	Mm_Celera	2:153141342	CACCTATAACTACAG[C/T]TCTAGAGAATCTGGC	15162
rs226340259	snp	C/T			intron-variant	Hck	Mm_Celera	2:153138008	GAGTTCAAGGCTGGC[C/T]AGGCTGGTCTACAAA	15162
rs226398769	snp	A/G			intron-variant	Hck	Mm_Celera	2:153145259	GTGTTCTTCATGATC[A/G]CCCCAGACTTAAACA	15162
rs226420518	snp	G/T			intron-variant	Hck	Mm_Celera	2:153144067	AAAAAGAAAAAAGAG[G/T]GAGGAGAGAATATTG	15162
rs226478918	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153107480	AAGGCAAAGAACTCC[C/T]GCGGGCGCCAGACTT	15162
rs226522762	snp	A/T			intron-variant	Hck	Mm_Celera	2:153110553	TCCAGCCCGAGAGAT[A/T]CTCACACCAGCATCA	15162
rs226592600	in-del	-/TC			upstream-variant-2KB	Hck	Mm_Celera	2:153108142	GTAAAATATTACAAT[-/TC]TTTAGGGAATCCAAG	15162
rs226614652	snp	A/C			intron-variant	Hck	Mm_Celera	2:153115112	CTAAAGCTAGACTGC[A/C]GGCCAGCATGCCCCA	15162
rs226767911	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153107176	GCTAACACCGCTCGC[A/G]CTCAGAATTCATACT	15162
rs226893518	snp	A/G			intron-variant	Hck	Mm_Celera	2:153112520	GGGTCCTCCAAGAGA[A/G]CTGCAAATGTTCTTA	15162
rs227090911	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153114211	TTGCTTTTTTCCCTC[-/T]TTTTTTCATGTGTGT	15162
rs227151891	snp	A/G			intron-variant	Hck	Mm_Celera	2:153138044	TTTCAGGACAGCCAG[A/G]ATGACACAGAGAAGC	15162
rs227186742	snp	A/C			intron-variant	Hck	Mm_Celera	2:153138703	GCGGTTGGTTGCGTG[A/C]AGATGCAGAACCCAT	15162
rs227208030	snp	C/T			intron-variant	Hck	Mm_Celera	2:153113469	CTGCTTCCATATACA[C/T]GTCAATAAGGCCAAG	15162
rs227298539	in-del	-/CAAG			intron-variant	Hck	Mm_Celera	2:153125961	CTCAAAAAAACAAAA[-/CAAG]CAGACTCTGGAGAAG	15162
rs227362943	snp	A/G			utr-variant-5-prime	Hck	Mm_Celera	2:153108587	ACCAAAGTCGCCCGT[A/G]AAGGGGGCTCTGACC	15162
rs227377754	snp	C/G			intron-variant	Hck	Mm_Celera	2:153134274	GAGCCTAAGCTGCTC[C/G]TCACTGCACAGTGTG	15162
rs227443881	snp	A/G			intron-variant	Hck	Mm_Celera	2:153135010	GGAACAGGCTACCTT[A/G]TGGGGCTAGCATACT	15162
rs227447818	snp	A/C			intron-variant	Hck	Mm_Celera	2:153119457	GATTTAAGGCCTGCT[A/C]TGCAGAAGGGAACCA	15162
rs227463094	snp	A/T			intron-variant	Hck	Mm_Celera	2:153109247	ACCCAGGCCTGGCTA[A/T]AGGTGTATATCTGAG	15162
rs227468894	in-del	-/GTAC			upstream-variant-2KB	Hck	Mm_Celera	2:153107290	GGAGGGAGGACTCCT[-/GTAC]GTTTCTGCAGGTGTG	15162
rs227489641	snp	A/G			intron-variant	Hck	Mm_Celera	2:153140979	GAAAGAAAAAAGAAA[A/G]AAAGAGCAACTCCTG	15162
rs227518857	snp	A/G			intron-variant	Hck	Mm_Celera	2:153141086	ATAGTCAGTGTTATC[A/G]TTTCAGAATACTAAG	15162
rs227551684	snp	C/T			intron-variant	Hck	Mm_Celera	2:153141411	CTGCACGCAACCAAC[C/T]GCACAGCAAGAATAT	15162
rs227658242	in-del	-/AGAGAGAGAGAGAG			intron-variant	Hck	Mm_Celera	2:153122259	AGCACCAGGAAAGGA[-/AGAGAGAGAGAGAG]AGAGAGAGAGAGAGA	15162
rs227779456	snp	G/T			intron-variant	Hck	Mm_Celera	2:153112147	ATTAATTTTGTTACT[G/T]CGAAGTTGTTCTACA	15162
rs227781918	snp	A/T			intron-variant	Hck	Mm_Celera	2:153110939	AAGTCCCTGGTTTGG[A/T]TCCCTCTCAGTTCTC	15162
rs227861002	snp	A/G			intron-variant	Hck	Mm_Celera	2:153112694	GCTGTTGTGGTGGGA[A/G]CCGTCACCTCCTCCT	15162
rs227965117	snp	G/T			intron-variant	Hck	Mm_Celera	2:153133061	GGCCACAGATTGGAA[G/T]GCTTGTGTATCTCTG	15162
rs228132848	snp	A/C			intron-variant	Hck	Mm_Celera	2:153128423	AAAACAAAACAAAAA[A/C]CCTCTGTACTTGGCT	15162
rs228134069	in-del	-/G			upstream-variant-2KB	Hck	GRCm38.p3	2:153107542	GGTGGAGGGAAAACC[-/G]GCTGCATGTGGGAGG	15162
rs228145650	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120779	AAATGCGTATGACAC[A/G]AAGTCTCTCACCTTA	15162
rs228154683	snp	A/T			intron-variant	Hck	Mm_Celera	2:153128853	TAACCAGCACCCTTG[A/T]ATAGTCTCTAAATTA	15162
rs228180778	snp	G/T			intron-variant	Hck	Mm_Celera	2:153111962	TAATGAGAAGAGTAT[G/T]GAGACTTGGAAAGTC	15162
rs228197275	snp	A/G			intron-variant	Hck	Mm_Celera	2:153140322	ACAGTGGCACAGATG[A/G]AAGGGATGTGGCATA	15162
rs228241842	snp	A/G			intron-variant	Hck	Mm_Celera	2:153127524	CACCCTCTTATTGAC[A/G]ATGAGAAGTCATGAA	15162
rs228245876	snp	C/T			intron-variant	Hck	Mm_Celera	2:153142782	CCCGAGCCCATAGTT[C/T]GAACAAAAAGCCTGC	15162
rs228330204	snp	A/G			intron-variant	Hck	Mm_Celera	2:153135037	TACTCAGGGCCTCTT[A/G]TGATGGTGAAAATTC	15162
rs228600792	snp	A/T			intron-variant	Hck	Mm_Celera	2:153122291	AGAAAAGAGGACCCC[A/T]CTCACCATCCTTCCT	15162
rs228794814	snp	A/T			intron-variant	Hck	Mm_Celera	2:153135878	GAGAGAGACAGAGAG[A/T]CAGAGACAGAGTAAT	15162
rs228801605	snp	C/T			intron-variant	Hck	Mm_Celera	2:153109686	TAGGTCTTAAAGAGA[C/T]ATTTGTGTATGTTAC	15162
rs228825466	snp	A/G			intron-variant	Hck	Mm_Celera	2:153138776	GACATCAAAACTACG[A/G]AATTTTTCATAACAG	15162
rs228881144	snp	C/T			utr-variant-3-prime	Hck	Mm_Celera	2:153151432	TATGAATGTCAAAGG[C/T]TTTCCCCAAGGGTCA	15162
rs228937566	snp	A/G			intron-variant	Hck	Mm_Celera	2:153124631	AACTATTGCTCAAGG[A/G]TGAGGGCCAGAGTTT	15162
rs228939404	snp	A/G			synonymous-codon	Hck	Mm_Celera	2:153134142	CTATAAGATCCGGAC[A/G]CTGGACAGTGGAGGC	15162
rs228967707	snp	A/G			intron-variant	Hck	Mm_Celera	2:153125074	TCGAGCCATAGAGAA[A/G]GAACCAGAAACAGTA	15162
rs229034514	snp	C/G			intron-variant	Hck	Mm_Celera	2:153132880	AAAACGCACACTGTT[C/G]CTGTCATTCACTGTT	15162
rs229038749	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153107742	ATGGGATTAAGGTCT[C/T]GTAGGGGGCTGGTGG	15162
rs229178835	in-del	-/G			intron-variant	Hck	Mm_Celera	2:153109172	GTGGCAGGTCACGCA[-/G]GGTAGACAGCAGCCA	15162
rs229234223	snp	G/T			intron-variant	Hck	Mm_Celera	2:153115255	TGAGCCATCTTCTCA[G/T]CCCCCTGGGCAACAT	15162
rs229244890	snp	C/T			intron-variant	Hck	Mm_Celera	2:153139513	TTTAAGTACAAACTG[C/T]GCACAATGGTGAATG	15162
rs229249229	in-del	-/C			intron-variant	Hck	Mm_Celera	2:153142632	GAGTTAGCATACCTT[-/C]CCCCATTGAGCTCAC	15162
rs229292185	in-del	-/AGGG			intron-variant	Hck	Mm_Celera	2:153148548	GAAGAATAGGAAGGA[-/AGGG]ACACTCTGACTAGGG	15162
rs229349493	snp	A/C			intron-variant	Hck	Mm_Celera	2:153130571	GCACACTCACACACA[A/C]ACACATACATATAGG	15162
rs229421923	in-del	-/GATGTGTACC			intron-variant	Hck	Mm_Celera	2:153127242	CCTGGGTCTTCTCCG[-/GATGTGTACC]GCCTGATTCTGAGGA	15162
rs229477654	snp	C/G			intron-variant	Hck	Mm_Celera	2:153109372	CACCATCTCCTCTGT[C/G]TGACACTGGGGCATG	15162
rs229523373	in-del	-/GTA			intron-variant	Hck	Mm_Celera	2:153110069	TTTACATCAATTGAT[-/GTA]AGCCTCAGATCAGGT	15162
rs229726174	snp	C/T			intron-variant	Hck	Mm_Celera	2:153124755	AATGAAGGAAGACAT[C/T]AACTTCGGGGGCTCC	15162
rs229729183	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153147393	ATGTGTCATCACCAC[-/T]GCCAGGAAGTTGAAA	15162
rs229752994	snp	G/T			intron-variant	Hck	Mm_Celera	2:153118179	TCAAGACAGGGTTTC[G/T]CTGTGTAGTCCTGGC	15162
rs229793944	snp	A/G			synonymous-codon	Hck	Mm_Celera	2:153124212	CCGAGATGGAAGCAA[A/G]GCCTCAAAAACAGAG	15162
rs229795847	snp	A/G			intron-variant	Hck	Mm_Celera	2:153132188	ACTGGCATTCCCATG[A/G]GTGAGTTTCCCCAGG	15162
rs229847980	snp	C/T			intron-variant	Hck	Mm_Celera	2:153123946	GCTCCATAGATCCGT[C/T]GTGCCATTTCCATTA	15162
rs230143536	snp	C/T			intron-variant	Hck	Mm_Celera	2:153141238	AAAATTATCCCAGGA[C/T]CTGGAGAGATGGCTC	15162
rs230172998	in-del	-/GAGA			intron-variant	Hck	Mm_Celera	2:153119144	GATCCACATGTGAGT[-/GAGA]GAATTTGACATCTGT	15162
rs230185489	snp	C/G			intron-variant	Hck	Mm_Celera	2:153147642	CCTTCCTCTGGTGCT[C/G]CTACTTTTGTGATGA	15162
rs230254111	snp	A/C			intron-variant	Hck	Mm_Celera	2:153140636	CTACAGCAAGAGCAA[A/C]TCCTGGGGGCTGGAG	15162
rs230404319	snp	C/T			intron-variant	Hck	Mm_Celera	2:153121999	AAGGTCCCTTGCTGC[C/T]GAGCAAGTGCCATGC	15162
rs230508729	snp	A/G			intron-variant	Hck	Mm_Celera	2:153124589	GGAGAGCAGCAGGGA[A/G]GCTGAGGGATCGCTC	15162
rs230515270	in-del	-/TGCACACACACA			intron-variant	Hck	Mm_Celera	2:153135832	TGACCTACACACACG[-/TGCACACACACA]TGCACACACACATGC	15162
rs230549885	snp	A/C			intron-variant	Hck	Mm_Celera	2:153129693	CCCAGACTCCTGTGG[A/C]GACTCCTCAGCACGT	15162
rs230844969	snp	C/T			intron-variant	Hck	Mm_Celera	2:153127739	CTCTCACTGTCTAGT[C/T]CAGGAGGATGCTTGG	15162
rs230901333	snp	C/T			intron-variant	Hck	Mm_Celera	2:153145949	TGCAGGCTTGTAATG[C/T]AGGCTACTCTGGAGA	15162
rs231102521	snp	A/G			intron-variant	Hck	Mm_Celera	2:153136339	CGTTAAGCAAGTTCT[A/G]TGCCATTGAGCACCA	15162
rs231124287	snp	C/T			intron-variant	Hck	Mm_Celera	2:153115926	AGGCCCCCTCAGTGG[C/T]TGCCATCCCCAGGAG	15162
rs231144002	snp	A/G			intron-variant	Hck	Mm_Celera	2:153128373	TTCTGAGTTGTAACT[A/G]ATGGGGGAAAGTAAA	15162
rs231148630	snp	C/T			intron-variant	Hck	Mm_Celera	2:153129267	GAGAATCTGACTGCA[C/T]ACCATATAGGACCTA	15162
rs231219216	in-del	-/AGGA			intron-variant	Hck	GRCm38.p3	2:153148540	GAGGAAGGGAAGAAT[-/AGGA]AGGAAGGGACACTCT	15162
rs231274200	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153121390	AGTTGTCTCATGAAG[-/T]TTTTTATAGTAACAA	15162
rs231340445	snp	C/G			intron-variant	Hck	Mm_Celera	2:153130253	GAGCTCTCACACCTG[C/G]GCTCTGGGGTTAGAC	15162
rs231387253	snp	A/T			intron-variant	Hck	Mm_Celera	2:153122378	TTACTTAATATGCAC[A/T]ATGATTGGGACCTAG	15162
rs231469386	snp	A/G			intron-variant	Hck	Mm_Celera	2:153140444	GGGGCTCAGATCCCG[A/G]GGAAGTCTAAGCAGA	15162
rs231538581	snp	C/T			intron-variant	Hck	Mm_Celera	2:153138457	CTAGTCACAGTACTC[C/T]AAGTACTCAAAGACT	15162
rs231575370	snp	C/T			intron-variant	Hck	Mm_Celera	2:153115201	CTAGGGACCAGGAGC[C/T]GGGGTCCTTACATTT	15162
rs231616370	snp	G/T			intron-variant	Hck	Mm_Celera	2:153139878	AGAGAAGGGGGCTAT[G/T]TAAGCCGCTGGGACA	15162
rs231677017	snp	C/T			intron-variant	Hck	Mm_Celera	2:153116949	TTCAGTTGTCTCCTT[C/T]AGGGTAGGTCTTGTT	15162
rs231683002	snp	A/G			intron-variant	Hck	Mm_Celera	2:153146221	ATATAATCTAAATCT[A/G]TAAAGAATAAGTGGG	15162
rs231698666	in-del	-/CACACACA			intron-variant	Hck	Mm_Celera	2:153109067	CAGGTTCCCCTTCTG[-/CACACACA]CACACACACACACAC	15162
rs231752567	snp	A/G			intron-variant	Hck	Mm_Celera	2:153145166	CAGATGAAAGAAGTG[A/G]ACCTAAACAGAGTAG	15162
rs231755315	snp	C/G			intron-variant	Hck	Mm_Celera	2:153137653	ACAAATCTACAACCA[C/G]CCAGCTTTCTAAAGC	15162
rs231769572	snp	A/C			intron-variant	Hck	Mm_Celera	2:153117149	CTGGGAAACAGCCAG[A/C]CAGGCTAACTGGCTT	15162
rs231828984	snp	C/G			intron-variant	Hck	GRCm38.p3	2:153143564	CGCTGGTCCTCCTGC[C/G]TTTGCATGTGGCAGT	15162
rs231829986	snp	G/T			intron-variant	Hck	Mm_Celera	2:153123779	GGGTGCCATTCAGAG[G/T]CTGTGCTGAGTGTTC	15162
rs231924383	snp	A/G			intron-variant	Hck	Mm_Celera	2:153114854	TGGGAATAACACAGC[A/G]GGTGAGAGTAAATGT	15162
rs231971223	snp	A/T			intron-variant	Hck	Mm_Celera	2:153145431	ATCTGTTACCCTTGA[A/T]ATGAAATTCCCAGAA	15162
rs232016736	snp	C/T			intron-variant	Hck	Mm_Celera	2:153113345	CAGACAGAGCAGATA[C/T]AGAGAGATCTCCATG	15162
rs232041948	snp	C/T			intron-variant	Hck	Mm_Celera	2:153149509	TCCCAAGTGCTGGGA[C/T]GAAAGGTCTACAGCA	15162
rs232117861	snp	A/G			intron-variant	Hck	Mm_Celera	2:153112309	TAATATTCCATTTTG[A/G]GGTGCACCATTTTTA	15162
rs232287268	snp	C/T			intron-variant	Hck	Mm_Celera	2:153126461	ACCATTCTTAGTGCT[C/T]CCCAAAGTGCAGTGC	15162
rs232365158	snp	C/G			intron-variant	Hck	Mm_Celera	2:153116397	TCAAATTAACCCAAG[C/G]AGCAGAGGAATTTAT	15162
rs232430584	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153131774	GCTTAGCTGGAGATG[-/T]CCGAGGTCATTTGAC	15162
rs232492012	snp	A/C			intron-variant	Hck	Mm_Celera	2:153123296	TAAGTTAATACACAG[A/C]AATGTCTGAGTGATA	15162
rs232550966	snp	A/C			intron-variant	Hck	Mm_Celera	2:153128602	ACTGAAGCAGAGAAA[A/C]GGTGCTTACTGGTTT	15162
rs232552507	in-del	-/ATCCTC			intron-variant	Hck	Mm_Celera	2:153114490	GGGGTTTAAACTCTG[-/ATCCTC]ATCCTCGTGCTTGCA	15162
rs232660197	snp	A/G			intron-variant	Hck	Mm_Celera	2:153120008	GAGTTCTCAAAGAAA[A/G]AAATACATGGTCAAT	15162
rs232768967	snp	C/T			intron-variant	Hck	Mm_Celera	2:153149718	GGACACCCGTATACA[C/T]ATGGTGTATATATGC	15162
rs232770919	in-del	-/TG			intron-variant	Hck	Mm_Celera	2:153114219	TTCCCTCTTTTTTCA[-/TG]TGTGTGTGTGTGTGT	15162
rs232844900	snp	A/G			intron-variant	Hck	Mm_Celera	2:153114053	CAAGTATACACACCC[A/G]TGTGCACACACCCAC	15162
rs232921088	snp	A/T			intron-variant	Hck	Mm_Celera	2:153112948	GACTTGCATGCATAG[A/T]TCCTTCTGCAATGGA	15162
rs233025207	snp	A/G			intron-variant	Hck	Mm_Celera	2:153121677	CTCTGGACCTGCAAC[A/G]TTGTAGCCTTTCTAC	15162
rs233030002	snp	A/G			intron-variant	Hck	Mm_Celera	2:153149102	AGGGACATGGGCTTA[A/G]GGGTGTCTCCAGCCC	15162
rs233113069	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153127626	ACCCTTTTCGGTGGA[-/T]TTTACCACCACACTA	15162
rs233161257	in-del	-/GAGAGA			intron-variant	Hck	GRCm38.p3	2:153147085	GGTGTGTGTGTGTGT[-/GAGAGA]GATGTGGATATTTCC	15162
rs233168380	snp	A/G			intron-variant	Hck	Mm_Celera	2:153129464	AGTCTTCACCATCAG[A/G]ACCTCTTACAAGAGT	15162
rs233192825	snp	A/C			intron-variant	Hck	Mm_Celera	2:153121159	ACTACATAAAGCTAG[A/C]CACAGCTGCACGTGT	15162
rs233219475	snp	C/G			intron-variant	Hck	Mm_Celera	2:153114917	TAAAGGGGACAGTCA[C/G]CTCCAGCCAAGAAGC	15162
rs233278421	snp	G/T			intron-variant	Hck	Mm_Celera	2:153143447	ATTATCATTCTTCAT[G/T]CTCAGAGTAAAATTC	15162
rs233302372	in-del	-/CA			intron-variant	Hck	Mm_Celera	2:153126227	CCACTCTGTCCTGGG[-/CA]CATGGAGCAGGTGTG	15162
rs233312672	in-del	-/AAA			intron-variant	Hck	Mm_Celera	2:153144322	TCTGACCCCCCCCCC[-/AAA]CAAATGCAGGGCTGA	15162
rs233356519	in-del	-/ACACATGTGA			intron-variant	Hck	Mm_Celera	2:153124823	CAGATGTGCATCCAC[-/ACACATGTGA]ACACATATAAACAGA	15162
rs233525189	snp	A/G			intron-variant	Hck	Mm_Celera	2:153133228	ATTTTGGAGTCTTGT[A/G]GGGGCGGGGGCAGGG	15162
rs233606941	in-del	-/C			intron-variant	Hck	GRCm38.p3	2:153111651	CCCGCAGTTTGTTTT[-/C]CCCCCGACTTATCAG	15162
rs233627904	snp	C/T			intron-variant	Hck	Mm_Celera	2:153140187	TCCAGTTCCAGGAGC[C/T]TGGGGGTTAGAAATT	15162
rs233699484	in-del	-/GCCTCA			intron-variant	Hck	Mm_Celera	2:153137432	CTCGTAGCTGTCCTG[-/GCCTCA]CCTCTCAAGTGCTGG	15162
rs233726202	snp	C/G			intron-variant	Hck	Mm_Celera	2:153147159	GGCCATAATACAAGC[C/G]TCGCCGAATTCCAAA	15162
rs234010561	snp	A/G			intron-variant	Hck	GRCm38.p3	2:153149872	GCTGGGGCAGGTGGT[A/G]GCACATGGGTACCTG	15162
rs234076875	in-del	-/A			intron-variant	Hck	Mm_Celera	2:153117989	ATCGCTGATAAAAAG[-/A]AAAAAACCCTGAAGA	15162
rs234076956	snp	C/G/T			intron-variant	Hck	GRCm38.p3	2:153149158	GTATGTCTATTACAC[C/G/T]CAGCTCTTGATCTTC	15162
rs234105594	snp	G/T			intron-variant	Hck	Mm_Celera	2:153149329	AGGTGGATGGGAAGA[G/T]CTGGAGAAGTAGCAT	15162
rs234243676	snp	A/G			intron-variant	Hck	Mm_Celera	2:153125920	CTAATCTAATCCGAG[A/G]ATGTTCTGCCAGTGA	15162
rs234285707	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153107467	TTCAGCCCAGAATAA[A/G]GCAAAGAACTCCCGC	15162
rs234328525	in-del	-/AAGGAAGGAAGGAAGGAAGGAAGG			intron-variant	Hck	Mm_Celera	2:153117697	AGAAAGAAAGAAAGA[-/AAGGAAGGAAGGAAGGAAGGAAGG]AAGGAAGGAAGGAAG	15162
rs234497480	in-del	-/AG			intron-variant	Hck	Mm_Celera	2:153125478	AGGAAAGAGAGAGAA[-/AG]AGAAAGAGAGAGGGA	15162
rs234570546	snp	C/T			intron-variant	Hck	Mm_Celera	2:153111158	AGAGTTTGGGGCCAG[C/T]CTGGGCTATGAGACC	15162
rs234606603	snp	A/C			intron-variant	Hck	Mm_Celera	2:153139782	GATGAGACCACAGGC[A/C]TTAAAGGAAGGGCTC	15162
rs234626818	snp	A/T			intron-variant	Hck	Mm_Celera	2:153118012	CCTGAAGAAACTAGG[A/T]ACAGAAGGAGTCGTC	15162
rs234677453	in-del	-/ACAT			intron-variant	Hck	Mm_Celera	2:153113180	CGCACACACACACAC[-/ACAT]ATCATATCACATCAC	15162
rs234824985	snp	A/G/T			intron-variant	Hck	Mm_Celera	2:153139702	CAGGGCTGATTAGAG[A/G/T]GAGGGGGTGGCTCCC	15162
rs234893550	snp	G/T			intron-variant	Hck	Mm_Celera	2:153126036	AGTGAGAGTTGTTGA[G/T]GCAGAGGTGAACGCT	15162
rs235103317	snp	A/G			intron-variant	Hck	Mm_Celera	2:153148353	AGTTGCTGAACTACA[A/G]TGTTCAGTAACTAAG	15162
rs235106925	in-del	-/T			upstream-variant-2KB	Hck	Mm_Celera	2:153107645	AGACTTAAAGGGAGC[-/T]ACATTCCTTCTGCGG	15162
rs235132671	snp	A/G			intron-variant	Hck	Mm_Celera	2:153141286	GCTGCTCTTCCAGAG[A/G]TCCTGGATTCAGTCC	15162
rs235138989	in-del	-/TGACTGAGTGAC			intron-variant	Hck	GRCm38.p3	2:153148150	GAGTGAGTGAGTGAG[-/TGACTGAGTGAC]TGAGTGAGTGACTGA	15162
rs235217790	snp	C/T			intron-variant	Hck	Mm_Celera	2:153141898	AGGCAGGCAAAACAC[C/T]AGTGCACATAAAATA	15162
rs235242924	snp	A/G			intron-variant	Hck	Mm_Celera	2:153134448	GGGGCCTGTCTCTCA[A/G]AACCCCAGTGGCATG	15162
rs235271748	in-del	-/CTT			intron-variant	Hck	Mm_Celera	2:153147831	GCAGCCTTCTAGCTC[-/CTT]CCGCCCTACAGCCCT	15162
rs235306862	snp	C/T			intron-variant	Hck	Mm_Celera	2:153138227	TTTCTCACTAAGGAG[C/T]AGTAGTCCATGTTCC	15162
rs235382950	snp	C/T			intron-variant	Hck	Mm_Celera	2:153133347	TAGCATGTTCACAAA[C/T]TGAGTCCTTTTGTTA	15162
rs235453236	snp	C/T			upstream-variant-2KB	Hck	Mm_Celera	2:153107218	ACTGCTAAACGCATG[C/T]CTACATGCACGCGTA	15162
rs235491672	in-del	-/GGAGGGG			intron-variant	Hck	Mm_Celera	2:153117459	TGAACCCCACTACAC[-/GGAGGGG]AGGGGGGGGGGTGAA	15162
rs235654668	snp	C/T			intron-variant	Hck	Mm_Celera	2:153120451	AGCAAGTGGAACCAG[C/T]CTAGAGATCTATCAG	15162
rs235656327	snp	A/T			intron-variant	Hck	Mm_Celera	2:153128491	AACTTGGGGGAGGAG[A/T]GGGTTTGTTTCATCT	15162
rs235692284	snp	A/T			intron-variant	Hck	Mm_Celera	2:153121087	ACCAGTCACTGGAAG[A/T]TGGCTCAGCAGTAAA	15162
rs235797554	snp	A/T			intron-variant	Hck	Mm_Celera	2:153128016	TAAGCAACACAGATC[A/T]GGACCAGTTCCCTCA	15162
rs235970144	snp	C/G			intron-variant	Hck	Mm_Celera	2:153131121	GGTGTTTGGGCCCCC[C/G]ATCTGAGTGGGCTGT	15162
rs235993441	snp	A/G			intron-variant	Hck	Mm_Celera	2:153109557	ATGGAGATGGTAAGA[A/G]GACAGGTTGAATGTT	15162
rs236129143	snp	G/T			intron-variant	Hck	Mm_Celera	2:153132263	CACAGCGAGCCTTTG[G/T]CTCTTTGAACTCAGA	15162
rs236130851	snp	A/G			intron-variant	Hck	Mm_Celera	2:153124511	CTGCAGCAGCATGCA[A/G]GCAGACCCATGATGA	15162
rs236311334	snp	A/G			intron-variant	Hck	Mm_Celera	2:153138538	CTATTTTCCCTAGGC[A/G]CATTCCCCTGCATGC	15162
rs236409134	snp	A/C			intron-variant	Hck	Mm_Celera	2:153128745	AAAAAAAAATCCCTG[A/C]AGACTTCCCCACCAG	15162
rs236411158	snp	C/T			intron-variant	Hck	Mm_Celera	2:153120790	ACACGAAGTCTCTCA[C/T]CTTAACCATTTTAAG	15162
rs236544628	in-del	-/AACC			intron-variant	Hck	Mm_Celera	2:153134377	TGGTTCTGGAGAAGG[-/AACC]AGAGTCTACTGCTTG	15162
rs236587818	snp	C/T			intron-variant	Hck	Mm_Celera	2:153128328	TCTGGAAGCTTGGGT[C/T]TCAGCATCAGATACA	15162
rs236649549	in-del	-/AG			intron-variant	Hck	GRCm38.p3	2:153131027	AAATAGCAAAGAAGA[-/AG]AAAAAAAAAAAAAAA	15162
rs236892006	snp	A/T			intron-variant	Hck	Mm_Celera	2:153147090	GTGTGTGTGTGAGAG[A/T]GATGTGGATATTTCC	15162
rs236996663	snp	C/T			intron-variant	Hck	Mm_Celera	2:153144837	TGCCAGTGTTAATAC[C/T]ACACAAGACTTGAAG	15162
rs236998302	in-del	-/T			intron-variant	Hck	GRCm38.p3	2:153149993	TGGCACATGGGCAGC[-/T]GGGACAGGTGTTGGC	15162
rs237127413	snp	C/G			intron-variant	Hck	Mm_Celera	2:153123117	CTGTGCCCTTAGCTC[C/G]CCACAGTTAAGTTTT	15162
rs237138208	in-del	-/CACACACACACA			intron-variant	Hck	Mm_Celera	2:153109066	CAGGTTCCCCTTCTG[-/CACACACACACA]CACACACACACACAC	15162
rs237171745	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153107557	CGCTGCATGTGGGAG[A/G]GACCGAAGTGGAAGG	15162
rs237470636	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153107964	GTTTTGCAGGTAAAG[A/G]CGCCTGGTGCCAAGC	15162
rs237536026	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153136236	TTTCAAGGCAGCGTT[-/T]AAGCTTACATGCTAT	15162
rs237557178	in-del	-/CCTGTAC			upstream-variant-2KB	Hck	Mm_Celera	2:153107287	AGAGGAGGGAGGACT[-/CCTGTAC]GTTTCTGCAGGTGTG	15162
rs237697968	snp	A/G			intron-variant	Hck	Mm_Celera	2:153146647	GCAAAATGCCCCTAC[A/G]TGTAAAATAAGTCAT	15162
rs237698538	snp	C/T			intron-variant	Hck	Mm_Celera	2:153144276	CCTAAGATAGGCAGG[C/T]AGAACAGTGCCGGTT	15162
rs237745179	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130685	AAGCTTAGTGGCACA[A/G]TTCTTTAATTCCAAC	15162
rs237789641	snp	C/T			intron-variant	Hck	Mm_Celera	2:153122866	GGGCTATGGTCATAA[C/T]GGAACCAAGTTCTCA	15162
rs237791417	in-del	-/ATGACATTACTAGCCACCTCTC			intron-variant	Hck	Mm_Celera	2:153142429	CGCTTGGCTGCTCTG[-/ATGACATTACTAGCCACCTCTC]AAGTGAATACTAGAT	15162
rs237819691	in-del	-/G			intron-variant	Hck	Mm_Celera	2:153140631	AAAGCTACAGCAAGA[-/G]GCAAATCCTGGGGGC	15162
rs237884122	snp	A/G			intron-variant	Hck	Mm_Celera	2:153149975	GGGCAGCTGGGACAG[A/G]TGTTGGCACATGGGC	15162
rs237904316	in-del	-/AAAGGTA			intron-variant	Hck	Mm_Celera	2:153115459	AGATGCTGCAGAGCC[-/AAAGGTA]ACGTCCTAAGATTTT	15162
rs238115066	snp	C/T			intron-variant	Hck	Mm_Celera	2:153142337	ACATCAGCTTATTAC[C/T]ATCAGGTCCCAGGGT	15162
rs238153737	snp	A/G			intron-variant	Hck	Mm_Celera	2:153122441	GTCACTGCCCAAGCA[A/G]GCGGGTGGAGCTGCC	15162
rs238182247	snp	A/T			intron-variant	Hck	Mm_Celera	2:153115629	TGGAACTTTTACTCC[A/T]CCTGAAAATGAAGGG	15162
rs238278881	snp	A/C			intron-variant	Hck	Mm_Celera	2:153141403	TTCTGCATCTGCACG[A/C]AACCAACCGCACAGC	15162
rs238319251	snp	C/T			intron-variant	Hck	Mm_Celera	2:153111371	AGCATTGCCTGAATA[C/T]ATGCATAGAAACTAA	15162
rs238332695	snp	G/T			intron-variant	Hck	Mm_Celera	2:153141541	GGTTTGGTTTGGTTT[G/T]GTTTTGTTGTTTTGT	15162
rs238341149	snp	C/T			intron-variant	Hck	Mm_Celera	2:153148112	AGGCTATGTAGTGAA[C/T]TGAGAGCCTGTCTCA	15162
rs238367079	snp	A/G			intron-variant	Hck	Mm_Celera	2:153147306	GCTCAGGCCTGCGCT[A/G]GGACTTTAACCATCT	15162
rs238380673	snp	G/T			intron-variant	Hck	Mm_Celera	2:153148864	CGCTATTTGTAGAGG[G/T]CATGATTCCCCTCAC	15162
rs238553328	snp	C/T			intron-variant	Hck	Mm_Celera	2:153118280	TGCTGGGATTAGAGG[C/T]GTGCGCCACCACTGC	15162
rs238666916	snp	A/C			intron-variant	Hck	Mm_Celera	2:153124871	GCATGCAAAACAAAA[A/C]AAATCAATAGTGACT	15162
rs238815169	snp	C/T			intron-variant	Hck	Mm_Celera	2:153126774	GGAGAGAAACGAGTC[C/T]ACCGGTCCCTTCTGA	15162
rs238852500	snp	A/G			intron-variant	Hck	Mm_Celera	2:153138093	CAAGAGAAAGGAGGA[A/G]GAGGAGGTGGTTAGC	15162
rs238964946	in-del	-/TCTGCCTCTGCCTCTGCC			intron-variant	Hck	Mm_Celera	2:153149464	AGTCCCAGAAACCCA[-/TCTGCCTCTGCCTCTGCC]TCTGCCTCTGCCTCC	15162
rs239050338	snp	A/C			intron-variant	Hck	Mm_Celera	2:153128200	GGGTTGAAAAGGGTG[A/C]CCTTTTCAACACAGG	15162
rs239065131	snp	A/G			upstream-variant-2KB	Hck	Mm_Celera	2:153107264	GATACTGGTGGTCTG[A/G]CCTGGCTAGAGGAGG	15162
rs239175840	snp	A/G			intron-variant	Hck	Mm_Celera	2:153142078	AATAAATTATATTTG[A/G]AGAGAGAGGGGAAGA	15162
rs239193006	snp	A/G			intron-variant	Hck	Mm_Celera	2:153141432	GCAAGAATATTCTAA[A/G]TCAAATGCAGCTTTC	15162
rs239363978	snp	C/G			intron-variant	Hck	Mm_Celera	2:153111209	CTTCAGTCAACAAGG[C/G]ATGTATCCTGAAATC	15162
rs239399595	snp	A/T			intron-variant	Hck	Mm_Celera	2:153136659	CTCCTCCAGGGCTGC[A/T]GGGTCCTAACCACCC	15162
rs239403325	in-del	-/A			intron-variant	Hck	Mm_Celera	2:153133624	AGATAAATGGTATAG[-/A]AAGATAGATAGATAG	15162
rs239449054	snp	A/G			intron-variant	Hck	Mm_Celera	2:153128525	AGTCTGTGGGTCACA[A/G]TCTGTCACTGAGGGA	15162
rs239640513	snp	A/T			intron-variant	Hck	Mm_Celera	2:153143732	GCCTTTTCTCTGTGG[A/T]GGTCATGCCGGCAAT	15162
rs239789961	in-del	-/T			intron-variant	Hck	GRCm38.p3	2:153129824	TGCCAGCTGATCCTC[-/T]TCTCCCTCCTTTTCC	15162
rs239814853	snp	C/T			intron-variant	Hck	Mm_Celera	2:153136359	ATTGAGCACCAGTCT[C/T]AACTCTTGTCTTCTG	15162
rs239815084	snp	A/T			intron-variant	Hck	Mm_Celera	2:153143893	GGAGAGTTGGATCAG[A/T]GGTTAAGAGCACTGA	15162
rs239844004	snp	A/T			intron-variant	Hck	Mm_Celera	2:153150709	AGACTGAGTTCCAGG[A/T]CAACCAATGCTACAA	15162
rs239969420	snp	A/G			intron-variant	Hck	Mm_Celera	2:153117237	TGGATTGCCCTAGAC[A/G]TGGTCAGCAGCTTTG	15162
rs239989057	snp	A/C			intron-variant	Hck	Mm_Celera	2:153113657	TACATTTATGTATCC[A/C]TGTGTGGATATATAC	15162
rs240001859	in-del	-/AACA			intron-variant	Hck	Mm_Celera	2:153123547	AATGCAACTTGAATG[-/AACA]AATGAATGAATGAAT	15162
rs240066681	snp	G/T			intron-variant	Hck	Mm_Celera	2:153119978	TCAATACATGGGATA[G/T]GACTGAATATGCCAG	15162
rs240085260	snp	C/T			intron-variant	Hck	Mm_Celera	2:153145230	CCAGGCAAAAGTCAT[C/T]TCTGAAGGTCACAGT	15162
rs240117625	in-del	-/TTCCAGAC			intron-variant	Hck	Mm_Celera	2:153142890	TAAATTTCCCATGCT[-/TTCCAGAC]CTCCAGACCCCGTCT	15162
rs240172164	snp	A/G			intron-variant	Hck	Mm_Celera	2:153110836	GGAACTCACCACCCA[A/G]AATTAACTAATTCAC	15162
rs240231150	in-del	-/AAC			intron-variant	Hck	Mm_Celera	2:153135457	GGGACAAACAAAACA[-/AAC]AAACAAACAAATAAA	15162
rs240238647	snp	A/G			intron-variant	Hck	Mm_Celera	2:153145760	TTATATATCATTAAA[A/G]CTGTAAAATTCACTT	15162
rs240402984	in-del	-/GG			intron-variant	Hck	Mm_Celera	2:153118761	TTGAAAACTAAATCA[-/GG]AAAAAAAAAATCCTA	15162
rs240444634	snp	C/G			intron-variant	Hck	GRCm38.p3	2:153140532	TGCATCTCAGTGGGT[C/G]GGGTCTTCTGGGAAA	15162
rs240455057	snp	C/G			intron-variant	Hck	Mm_Celera	2:153121794	GAAGGTCAGCAGACA[C/G]AGTTGTCCTCTGAAA	15162
rs240580553	in-del	-/T			intron-variant	Hck	Mm_Celera	2:153109436	CTGTAAAATGGGCTG[-/T]TTTTACATTCATCTG	15162
rs240610161	snp	C/G			intron-variant	Hck	Mm_Celera	2:153137819	CTGCAGCTGGGCGGG[C/G]ATAAATGCTGGGAGT	15162
rs240757337	in-del	-/C			intron-variant	Hck	Mm_Celera	2:153149181	TGATCTTCCCCCAGT[-/C]CCTCTCCACCTTTCT	15162
rs240857097	snp	A/G			intron-variant	Hck	Mm_Celera	2:153125871	AGTGGAGAGGCAGAG[A/G]CAAGCAGATTCCTGG	15162
rs240876960	snp	A/G			intron-variant	Hck	Mm_Celera	2:153109146	CGTTCAGTTCCCATT[A/G]ATGGTGGGTGGGTGG	15162
rs240998981	snp	A/G			intron-variant	Hck	Mm_Celera	2:153130585	ACACACATACATATA[A/G]GAGAGAGAGAGAGAG	15162
rs241010041	snp	A/G			intron-variant	Hck	Mm_Celera	2:153132804	ATACGTCTATAAAGC[A/G]TCTGCCTCGTGAGAC	15162
rs241101951	snp	A/G			intron-variant	Hck	Mm_Celera	2:153140089	CTCTGCTCTCTGGGG[A/G]GAAACCTGGTGGACA	15162
rs241240745	in-del	-/AGAAAAGAGAAAAG			intron-variant	Hck	Mm_Celera	2:153117735	GGAAGAAAGGAAGAA[-/AGAAAAGAGAAAAG]AGAAAAGAGAAAAGA	15162
rs241242005	snp	C/G			intron-variant	Hck	Mm_Celera	2:153109205	GCTAAAGGAACAGCC[C/G]GGCCAAGACAAGCCC	15162
rs241242371	snp	C/G			intron-variant	Hck	Mm_Celera	2:153117441	CAGAGAGGGAGGGCG[C/G]GGGTGAACCCCACTA	15162
rs241276551	snp	C/T			intron-variant	Hck	Mm_Celera	2:153110663	CCTCCGGGCTGCTGA[C/T]GCTGCCCAGAAATCT	15162

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