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

Stam

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs258399603	snp	A/T			intron-variant	Stam	Mm_Celera	2:14142594	GTAGCTGAGACTAAC[A/T]ACTGTAGTTCACACT	20844
rs258432379	snp	A/C			intron-variant	Stam	Mm_Celera	2:14088191	GGAGGCTAGGAGATA[A/C]AAGTTTCTGACCTGG	20844
rs258471489	snp	G/T			intron-variant	Stam	Mm_Celera	2:14086658	TCCCTGGGGCTTCCA[G/T]CCACTTGAGGGTTAG	20844
rs258507017	snp	A/G			intron-variant	Stam	Mm_Celera	2:14104783	GTATTTTAGTAATTT[A/G]TGTAGTGAATCTACG	20844
rs258515691	snp	C/T			intron-variant	Stam	Mm_Celera	2:14087758	GGATTTTTCATTACT[C/T]TTTGCCCCTCTAATA	20844
rs258552586	snp	C/T			intron-variant	Stam	Mm_Celera	2:14105145	GATTTCTGTACTTCT[C/T]TAGTCTTCCACAAAG	20844
rs258663575	in-del	-/CACT			intron-variant	Stam	Mm_Celera	2:14110861	CCCCCTCCCCCCCCA[-/CACT]CACTCACTCACTCAC	20844
rs258672140	snp	C/T			intron-variant	Stam	Mm_Celera	2:14104063	ATGGGAAGAGTCAGG[C/T]AGGGTGAGGATGGAG	20844
rs258746929	snp	C/G			intron-variant	Stam	Mm_Celera	2:14094155	TGTGTTCTAAAGTTT[C/G]TTTTTGGAGGCAGTC	20844
rs258784632	snp	G/T			intron-variant	Stam	Mm_Celera	2:14108135	TTTTCTATGGCTTGC[G/T]CAGCCTGCTTTCTTA	20844
rs258947576	in-del	-/T			intron-variant	Stam	Mm_Celera	2:14104157	TGCATGCATTCTCTG[-/T]TTACCTTTGATGTCC	20844
rs258954054	in-del	-/TT			intron-variant	Stam	Mm_Celera	2:14107807	TCGTTACTCACATGA[-/TT]TTTTTTGGCTCCAGC	20844
rs258987132	snp	C/G			intron-variant	Stam	Mm_Celera	2:14128668	ATTCTGGAATGGGAA[C/G]GAAGAAGACAGGTCC	20844
rs258992873	snp	C/G			intron-variant	Stam	Mm_Celera	2:14111463	AAGTAACTGTGTCTG[C/G]TATGAGTTCATGGTT	20844
rs259019500	snp	G/T			intron-variant	Stam	Mm_Celera	2:14144438	ATGTAGAATTTGGAA[G/T]TGTGGTCCCTGACAC	20844
rs259086043	snp	A/G			intron-variant	Stam	Mm_Celera	2:14103275	ACAAATGTCTTATTT[A/G]GGAATCGTTCATAAG	20844
rs259120177	snp	A/C			intron-variant	Stam	Mm_Celera	2:14113907	AGCAAGTTCTTTGCC[A/C]GAATGTAACACAAAT	20844
rs259143732	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14081623	TTCAATTCTATTCCA[G/T]TGGTCTACTTGTCTG	20844
rs259178187	in-del	-/T			intron-variant	Stam	Mm_Celera	2:14108803	AATTTGGTGGACACA[-/T]TTTTCAAATGAGGTT	20844
rs259290902	snp	C/T			intron-variant	Stam	Mm_Celera	2:14135719	TGGTACCTACAGAGG[C/T]TAGAAAGGGCATTAG	20844
rs259342185	snp	A/G			intron-variant	Stam	Mm_Celera	2:14144316	TTCTCCTGCTAAACA[A/G]ACACTTGTTTTCATA	20844
rs259613763	snp	A/G			synonymous-codon	Stam	Mm_Celera	2:14141713	ATAGGTATATCCAGG[A/G]CCTGCGCAGAGCGGT	20844
rs259619637	snp	A/G			upstream-variant-2KB, intron-variant	Stam, Stamos	Mm_Celera	2:14072562	GCTCATCCTCAGTCA[A/G]TCTTTAAAGCCTTTT	20844
rs259651785	snp	C/T			intron-variant, upstream-variant-2KB	Stamos, Stam	Mm_Celera	2:14071994	ATCCATACTAATATA[C/T]GTTATTTCTGATTTT	20844
rs259712696	snp	A/T			intron-variant	Stam	Mm_Celera	2:14087123	TGGGATGGCAACCCC[A/T]TTCCTCACTTGATGT	20844
rs259923245	snp	A/T			intron-variant	Stam	Mm_Celera	2:14076284	CATGTTTTTTTAGAA[A/T]TCACTCTGAATTATA	20844
rs259997543	snp	C/G			intron-variant, upstream-variant-2KB	Stamos, Stam	Mm_Celera	2:14072052	GTAGTGTTTTGCTAG[C/G]TAACAACCTAACAAT	20844
rs260031195	in-del	-/GA			intron-variant	Stam	Mm_Celera	2:14140059	GGGGAATGGGGGGGG[-/GA]GAGAAGGAGGGTGAA	20844
rs260046786	snp	A/G			intron-variant	Stam	Mm_Celera	2:14099670	TTCTCTATGGTCTCT[A/G]CTTTAGTTCCTACCT	20844
rs260078075	snp	C/T			intron-variant	Stam	Mm_Celera	2:14131508	TCATCCCCGAGAAAG[C/T]GTGGCAAATGCAGTG	20844
rs260111399	snp	C/T			intron-variant	Stam	Mm_Celera	2:14130485	CATTAACGGCTGAAA[C/T]AGAGTATTTGATTCT	20844
rs260148075	snp	A/C			intron-variant	Stam	Mm_Celera	2:14140462	AACAGTTCACCGCCC[A/C]ACAAACACAGTCTTG	20844
rs260172735	snp	A/C			intron-variant	Stam	Mm_Celera	2:14131309	TCCAGGATATGAAGG[A/C]GTGGTGCTACACAGC	20844
rs260213862	snp	C/T			intron-variant	Stam	Mm_Celera	2:14140938	TAACTCCTCCTAGAT[C/T]CTCTCATCTCCATAC	20844
rs260275910	snp	A/G			intron-variant	Stam	Mm_Celera	2:14139691	GCTGCACAGAGGCCA[A/G]GAATGATAGGTTCTC	20844
rs260310605	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	Stam, Stamos	Mm_Celera	2:14073984	AGAGGAAGAGACAGC[A/G]GCGGCTCATCGCGTG	20844
rs260342326	snp	C/G			intron-variant	Stam	Mm_Celera	2:14102800	CCTGAGTTCCTGATA[C/G]AGTGTAATCAGCTGC	20844
rs260385016	snp	G/T			intron-variant	Stam	Mm_Celera	2:14134224	TATCAAGTACTGTTC[G/T]CTGTTGTCTATGCTG	20844
rs260416824	snp	A/T			intron-variant	Stam	Mm_Celera	2:14142905	CTTTAACCCCTTAGT[A/T]ACTGTACTAACAGTG	20844
rs260421274	in-del	-/TTT			upstream-variant-2KB, intron-variant	Stam, Stamos	Mm_Celera	2:14072470	CATATATTTGAAGGC[-/TTT]TTTTTTTTTCTTTTT	20844
rs260546481	snp	C/T			intron-variant	Stam	Mm_Celera	2:14139911	AGGAGATTAGATGCA[C/T]GCTCCTTAGAGGGAA	20844
rs260681843	snp	A/G			intron-variant	Stam	Mm_Celera	2:14128486	GAGGGCTCTTGTGAG[A/G]TTTTAGGTTAGAGAT	20844
rs260692230	in-del	-/AGA			intron-variant	Stam	Mm_Celera	2:14112155	TTTTTTAATTGGGTT[-/AGA]AGATTGTAGTTTTTA	20844
rs260711223	snp	G/T			intron-variant	Stam	Mm_Celera	2:14139174	ATATTAAAGAAAATA[G/T]ATTTTTGTAAAATGC	20844
rs260718515	snp	A/G			intron-variant, downstream-variant-500B	Stam	Mm_Celera	2:14138330	GTTTGGATCCTTAAA[A/G]CCCACATGTGGTGGG	20844
rs260723671	snp	G/T			intron-variant	Stam	Mm_Celera	2:14104756	ACCAACCAAAAATAC[G/T]TTCTTATTTCCGTAT	20844
rs260753077	snp	A/G			intron-variant	Stam	Mm_Celera	2:14103853	ACTGAAATTTGAGTA[A/G]CTACTGTGTATCAGT	20844
rs260754456	snp	A/C			intron-variant	Stam	Mm_Celera	2:14115673	TCTGCTAAGCAAGAA[A/C]ATGTGTTACCTTTGG	20844
rs260784700	snp	C/T			intron-variant	Stam	Mm_Celera	2:14114647	CCTAATGTCCGCAAA[C/T]ACCTCAATATTAATT	20844
rs260826162	snp	A/G			utr-variant-3-prime	Stam	Mm_Celera	2:14147066	ACTAATTATGAACAA[A/G]CCATGTATGTTATAT	20844
rs260986580	snp	G/T			upstream-variant-2KB, intron-variant	Stam, Stamos	Mm_Celera	2:14073409	GCTCCATTTTTCATG[G/T]GTGTGTGTGTGTTTT	20844
rs261010945	snp	G/T			downstream-variant-500B	Stam	Mm_Celera	2:14149220	TTTCCAGTATAGAGG[G/T]CTTTCATGGGTGACA	20844
rs261039839	snp	A/C			intron-variant	Stam	Mm_Celera	2:14110144	TAGGCAACCTACGAC[A/C]AGTTCGTCTCTGCAT	20844
rs261070795	snp	A/G			intron-variant	Stam	Mm_Celera	2:14126800	TGTTTAACAAGTAAT[A/G]AAAAAATCATATAAG	20844
rs261099222	snp	C/T			intron-variant	Stam	Mm_Celera	2:14126131	AGGCTTGTGACTGTG[C/T]TTTAGTTATTATTAT	20844
rs261132748	snp	C/T			upstream-variant-2KB, intron-variant	Stam, Stamos	Mm_Celera	2:14073491	GAAGGTCTAATCTTC[C/T]CAGGGACTCAGTGAC	20844
rs261144751	snp	G/T			intron-variant	Stam	Mm_Celera	2:14098780	GGAAGCATCAGAAAT[G/T]ATTAGTTCAGAACTG	20844
rs261236875	snp	C/T			intron-variant	Stam	Mm_Celera	2:14136406	ATGGCAGGCAAGTGA[C/T]CTTCTGGTGAGGCAC	20844
rs261466056	snp	A/G			intron-variant	Stam	Mm_Celera	2:14126366	AAGACGTGTTTAATG[A/G]AGAACAAATAATATA	20844
rs261494912	snp	A/G			intron-variant	Stam	Mm_Celera	2:14087902	GTGAACTTTGGGTTC[A/G]CTATCATGTGAAGCA	20844
rs261495748	snp	A/G			intron-variant	Stam	Mm_Celera	2:14137682	AAAGGAAACATTACG[A/G]CCGGGCTGTGGTGGC	20844
rs261579776	in-del	-/C			intron-variant	Stam	GRCm38.p3	2:14079517	CTTCTTCTTCTTCTT[-/C]CTTCTTCTTCCTTCT	20844
rs261592033	snp	C/G			intron-variant	Stam	Mm_Celera	2:14130442	ACCAGTGTCAAAGCT[C/G]GAAAGGAGAAGTGTA	20844
rs261667062	in-del	-/T			intron-variant	Stam	Mm_Celera	2:14105254	CTTGGTTAATTGTAC[-/T]TTTTTTTTTTGAGTT	20844
rs261734163	snp	A/G			intron-variant	Stam	Mm_Celera	2:14126669	TAATGGCTCTCAACG[A/G]TACGAACTGAAGAGC	20844
rs261754798	snp	A/G			intron-variant	Stam	Mm_Celera	2:14137910	TTGAATCTTGAGTAG[A/G]AGTTGAAATCACAAA	20844
rs261820055	snp	A/G			intron-variant	Stam	Mm_Celera	2:14134848	TGTTTTCTTTTTAAC[A/G]TTTAGTTTAATTTTC	20844
rs262010944	in-del	-/A			intron-variant	Stam	Mm_Celera	2:14088556	AGAACCCTGACTAAT[-/A]ACAGTCTCTTAAAGC	20844
rs262169512	snp	C/G			intron-variant	Stam	Mm_Celera	2:14110906	AAATAAATATAAAAT[C/G]TTTCCTTAAGGTATT	20844
rs262224767	snp	C/T			intron-variant	Stam	Mm_Celera	2:14107409	TTTTTTTCATTGTGT[C/T]TTTACACAGATAGGA	20844
rs262244669	snp	G/T			intron-variant	Stam	Mm_Celera	2:14118174	CTAAGTAGAGCCTTA[G/T]TCTTCTGCCTTCCGT	20844
rs262359613	in-del	-/A			intron-variant	Stam	Mm_Celera	2:14114609	TGTTTCCTCTTTGTG[-/A]ATTATTATTCATTAC	20844
rs262383357	snp	C/T			utr-variant-3-prime	Stam	Mm_Celera	2:14148188	ACTTCATAAGCAGTT[C/T]GATTATAATTTTTTA	20844
rs262419543	snp	C/T			intron-variant	Stam	Mm_Celera	2:14114338	TATATGATGTATACG[C/T]GTGGGCGTGCATGTG	20844
rs262439034	snp	A/G			intron-variant	Stam	Mm_Celera	2:14131372	ACTTTGTTTCTAAAA[A/G]TCAAATAAAGATCCT	20844
rs262460732	in-del	-/T			intron-variant	Stam	Mm_Celera	2:14108044	GGAGGGACATGTTTA[-/T]TTTTTTTATACTTCC	20844
rs262476836	snp	C/T			intron-variant	Stam	Mm_Celera	2:14145949	AGCAAGACTCCTTGG[C/T]CCCTGTACTTCTGGT	20844
rs262484628	snp	A/C			intron-variant	Stam	Mm_Celera	2:14107799	TCAGAATTCTCGTTA[A/C]TCACATGATTTTTTG	20844
rs262505651	snp	A/T			intron-variant	Stam	Mm_Celera	2:14118422	GATTGGACAAGTTCT[A/T]GTTATGTGAGGCTAT	20844
rs262536441	in-del	-/G			intron-variant	Stam	Mm_Celera	2:14104081	GTGAGGATGGAGGGT[-/G]GGGTGGTCCTGAACT	20844
rs262548340	snp	A/T			intron-variant	Stam	Mm_Celera	2:14116839	TAGAATTTAATGTCC[A/T]ATTAAGTCTTCATCT	20844
rs262572170	in-del	-/TTA			intron-variant	Stam	Mm_Celera	2:14102945	ACAACTACGATGGCC[-/TTA]ACGTGGCCTTGAGGG	20844
rs262747889	snp	A/C			intron-variant	Stam	Mm_Celera	2:14089362	TAAGTGGCACTTGTA[A/C]AAAAACAAGCCTAGT	20844
rs262766978	snp	A/T			intron-variant	Stam	Mm_Celera	2:14113042	ATGTTTAGGTTTTTT[A/T]AAAAAATTCTTATAT	20844
rs262931403	snp	A/C			intron-variant	Stam	Mm_Celera	2:14115767	CCTTCCCATTTGTAC[A/C]CTGATTGGAGGGACC	20844
rs262937745	snp	A/G			intron-variant	Stam	Mm_Celera	2:14097029	CTTCTTTTTAATTCT[A/G]CAGCGCTATCTTCCC	20844
rs262950842	snp	C/G			intron-variant	Stam	Mm_Celera	2:14132690	CACACTGACACACAC[C/G]GACATGTATGCATAG	20844
rs262960234	snp	A/C			intron-variant	Stam	Mm_Celera	2:14109829	CCCTGGAAAAAGCTA[A/C]TTCTGTCCCTCCTCA	20844
rs263057980	snp	C/G			intron-variant	Stam	Mm_Celera	2:14142199	ATGTTGTCATGTCCC[C/G]GATGTTAACGTGACT	20844
rs263097121	snp	A/G			intron-variant	Stam	Mm_Celera	2:14145226	TTGATTCTCAGTGAG[A/G]ACTCTTAGTATCTAC	20844
rs263128695	in-del	-/AAACAG			intron-variant	Stam	Mm_Celera	2:14111972	GATGTATAATGTCTT[-/AAACAG]TACGTCCTGCTCTGG	20844
rs263169199	snp	G/T			intron-variant	Stam	Mm_Celera	2:14103655	ACTTCAGAAGACACC[G/T]TTGAGTAGTCAGTTC	20844
rs263181993	snp	C/T			intron-variant	Stam	Mm_Celera	2:14102188	TTGAGTGAAGAAAGA[C/T]CCGTGGCTTTCAAGT	20844
rs263201819	snp	C/T			intron-variant	Stam	Mm_Celera	2:14112758	TAGTTTAATGAGGAC[C/T]CTCCAGTTGTTTTTT	20844
rs263328134	snp	C/T			intron-variant	Stam	Mm_Celera	2:14105501	TAGAGACACGAGTTC[C/T]GGGCTACTGGTTATT	20844
rs263342613	snp	C/T			utr-variant-3-prime	Stam	Mm_Celera	2:14149124	TGCCCTTCCTACTCA[C/T]TTCTTTCTTTCTTAC	20844
rs263441782	snp	G/T			intron-variant	Stam	Mm_Celera	2:14100508	ATAAGAATCTTAGTA[G/T]TATTGGTTGATCTGT	20844
rs263456438	snp	C/G			intron-variant	Stam	Mm_Celera	2:14112071	CTGCTCTTATGGAGA[C/G]TTCCCACACTAGCAC	20844
rs263548772	snp	A/G			intron-variant	Stam	Mm_Celera	2:14110501	AGACATCACAGTTGG[A/G]TAGGCCTATTGATTG	20844
rs263628627	snp	C/G			intron-variant	Stam	Mm_Celera	2:14114543	TGTGCACTAAAGTAT[C/G]GAAAGCATCTGGGGG	20844
rs263635155	snp	A/C			intron-variant, upstream-variant-2KB	Stam, Stamos	Mm_Celera	2:14074403	GCCGACTCCCGTCCC[A/C]CTGCGTTCGTTCATT	20844
rs263740014	snp	A/G			intron-variant	Stam	Mm_Celera	2:14140379	AGTCCCCATGAAGGA[A/G]AAAGCCACCACCCAC	20844
rs263800624	in-del	-/AA			intron-variant, upstream-variant-2KB	Stamos, Stam	Mm_Celera	2:14071941	AAGATCCCCAATAGC[-/AA]AGTCATTCTTCTATG	20844
rs263855214	snp	A/C			intron-variant	Stam	Mm_Celera	2:14132624	TTGCCCTTCTAGGGT[A/C]CCTGTAAGTGCATGC	20844
rs263888159	snp	A/G			upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime	Stam, Stamos	Mm_Celera	2:14073750	CTTTCTAGAGGGATT[A/G]CAACATCACAACAAC	20844
rs263944794	snp	C/T			intron-variant	Stam	Mm_Celera	2:14141886	ACCCGAAGTAATTTG[C/T]TATTGATGGTTGTTG	20844
rs263957377	snp	A/G			intron-variant	Stam	Mm_Celera	2:14102221	AGTAAAGAGCAACTG[A/G]AGTGTGAATAGGGAA	20844
rs264008407	in-del	-/AGG			intron-variant	Stam	Mm_Celera	2:14139774	CAAAGGGAAAGGGGT[-/AGG]AGGAGAGCTCTGGCC	20844
rs264056926	snp	A/C			intron-variant	Stam	Mm_Celera	2:14086619	TCTCCATGTGGGGAC[A/C]CCCACCCCACCTGAC	20844
rs264096172	snp	C/T			utr-variant-3-prime	Stam	Mm_Celera	2:14147937	ATATTTACAGCCCTT[C/T]TTTGGTTTTTCGAGA	20844
rs264185130	snp	A/T			intron-variant	Stam	Mm_Celera	2:14131737	AGAAGTAGTACTGGC[A/T]GCTGTAATGTAAGTA	20844
rs264201144	snp	C/T			intron-variant	Stam	Mm_Celera	2:14141177	AAAGTAAAATCTGCT[C/T]ATATAATGCTTAAAA	20844
rs264277099	snp	A/G			intron-variant	Stam	Mm_Celera	2:14096502	AAGTTCTGTCGCTTC[A/G]GCCTGTCCCAGAAAC	20844
rs264367134	snp	C/T			upstream-variant-2KB, intron-variant	Stam, Stamos	Mm_Celera	2:14072375	ATTTTAACTCCACCC[C/T]TTTGAAAGAAAAATT	20844
rs264388868	snp	A/G			intron-variant	Stam	Mm_Celera	2:14100276	GGTGGATGGGTGGGA[A/G]GGAGAGAGAGAATAA	20844
rs264414551	in-del	-/TATTA			intron-variant	Stam	Mm_Celera	2:14138002	ATTTTAAATTGTCAC[-/TATTA]TATTTTTAAAAAATC	20844
rs264427636	snp	A/G			intron-variant	Stam	Mm_Celera	2:14144723	GATAGGAGACCAGCT[A/G]AGAAGGCCAAACACT	20844
rs264485645	snp	C/T			intron-variant	Stam	Mm_Celera	2:14139420	AGGTGCTTGGTTTCT[C/T]GGTGATTGTGCTAGT	20844
rs264488008	snp	C/G			intron-variant, upstream-variant-2KB	Stamos, Stam	Mm_Celera	2:14071861	CACCTTTTATATTTG[C/G]CTTTTCTTGTACATA	20844
rs264537338	snp	A/G			utr-variant-3-prime	Stam	Mm_Celera	2:14147268	GAAGTAAGGGCATTG[A/G]TTTCCTTTGTCATAG	20844
rs264568982	snp	C/G			intron-variant, upstream-variant-2KB	Stamos, Stam	Mm_Celera	2:14071722	ATTAAACATATTATA[C/G]AAACATTTTAATGTG	20844
rs264627578	snp	A/T			intron-variant	Stam	Mm_Celera	2:14126923	AAATTAAAAGATTTT[A/T]AAATTGTGTTTAAAT	20844
rs264639243	snp	A/C			intron-variant, downstream-variant-500B	Stam	Mm_Celera	2:14138437	CTGCCCGGCCAGCCA[A/C]AGTGACTGGATGAGC	20844
rs264682223	snp	C/T			intron-variant	Stam	Mm_Celera	2:14112286	TCCCCTCTGATCTTT[C/T]ATTTTTACCTGTGTT	20844
rs264691734	snp	C/T			intron-variant	Stam	Mm_Celera	2:14128732	CAGATAAAGTAGGGC[C/T]GCTTCATTTTTAATG	20844
rs264789355	snp	A/G			intron-variant	Stam	Mm_Celera	2:14136082	AGTTTCATCTATACT[A/G]TCATAAAATAGGAAT	20844
rs264803427	in-del	-/C			intron-variant	Stam	Mm_Celera	2:14110959	CTCTCTTGTATTGAT[-/C]CCCCCCTCCCCTCTT	20844
rs264816903	snp	A/C			intron-variant	Stam	Mm_Celera	2:14142282	GCTCAGATTATATCT[A/C]ACACACTGACTCCAT	20844
rs264961702	snp	C/T			intron-variant	Stam	Mm_Celera	2:14117981	TGGCTCAGGTAATAA[C/T]GGACAGTCTTGTTAA	20844
rs264996851	snp	A/C			intron-variant	Stam	Mm_Celera	2:14125918	GTTTAGATCAGACTT[A/C]ATGGGGCAGGAAATA	20844
rs265115783	snp	A/G			utr-variant-3-prime	Stam	Mm_Celera	2:14147125	TGTCACCATACCAGC[A/G]TACGGTAGCCACAGT	20844
rs265324859	snp	A/G			intron-variant	Stam	Mm_Celera	2:14105433	TTTGCAAGTCCAAAG[A/G]GCCTCTCTTTCCAGT	20844
rs265383498	snp	C/G			intron-variant	Stam	Mm_Celera	2:14115035	TTCTGTTTCTGTTAT[C/G]TGGTAGTTAGCCTAA	20844
rs265393631	snp	A/G			intron-variant	Stam	Mm_Celera	2:14131787	CCCTTTAATAGTGCT[A/G]TGTCCTGTCTCTAGA	20844
rs265429844	snp	A/T			intron-variant	Stam	Mm_Celera	2:14143224	TGTATAAGAAGTACT[A/T]AGCATATGTTCACTA	20844
rs265443631	in-del	-/GGGGGGGGGG			intron-variant	Stam	Mm_Celera	2:14116240	CACATGAACTTCTTT[-/GGGGGGGGGG]GGGTAGTTCTTCTGC	20844
rs265551552	snp	G/T			intron-variant	Stam	Mm_Celera	2:14107172	GGACTCTTACCTGCT[G/T]AGCTGCCTCTCTATT	20844
rs265656416	snp	A/G			intron-variant	Stam	Mm_Celera	2:14099640	GCCATGAAGAATAAC[A/G]TCAGTAAGTCTCATT	20844
rs265693014	snp	C/T			intron-variant	Stam	Mm_Celera	2:14111365	CCGATAGCCTACGGT[C/T]GAGCAGTAAGGGGCA	20844
rs265744563	snp	C/T			intron-variant	Stam	Mm_Celera	2:14102787	GTCCCCTCTGCTTCC[C/T]GAGTTCCTGATACAG	20844
rs265754358	snp	A/T			intron-variant	Stam	Mm_Celera	2:14113176	CTTTCTTGGGTTGAC[A/T]CCACTTACTGCTTGT	20844
rs265890321	snp	A/T			upstream-variant-2KB, intron-variant	Stam, Stamos	Mm_Celera	2:14072899	CTGTAAGATTTAAAA[A/T]TCAGAATAACTGGAA	20844
rs265900207	snp	C/T			intron-variant	Stam	Mm_Celera	2:14101045	CTTCAAGCTAAGGAA[C/T]TTTCCCACCTCAAGG	20844
rs265953889	snp	A/G			intron-variant, upstream-variant-2KB	Stam, Stamos	Mm_Celera	2:14075559	GCTTATAATAAAACA[A/G]TATTTGCTGCCTCTG	20844
rs266020070	snp	C/T			intron-variant	Stam	Mm_Celera	2:14130591	TATAAACATTACACG[C/T]GTGATTTGACAAACT	20844
rs266029328	snp	A/G			intron-variant	Stam	Mm_Celera	2:14140584	TTGCTCATAATGGTA[A/G]GATAATTCTGAACAG	20844
rs266049225	snp	A/G			intron-variant	Stam	Mm_Celera	2:14097660	GGCAGCTCTCATAAG[A/G]ACAGCATTTAATTGG	20844
rs266117228	snp	A/G			intron-variant	Stam	Mm_Celera	2:14137213	TCTCGAACATGATAT[A/G]AGAGATTGTGGAGAT	20844
rs266128613	snp	C/T			intron-variant	Stam	Mm_Celera	2:14145570	ACATCTGTTCCTGTT[C/T]CCATGTGAGCCTGTC	20844
rs266182353	snp	A/G			synonymous-codon	Stam	Mm_Celera	2:14139031	GAAGTTAATGAATGA[A/G]GACCCAATGTACTCT	20844
rs266192974	snp	C/G			intron-variant, utr-variant-3-prime	Stam	Mm_Celera	2:14148538	AAAGTTGAGGGGTAA[C/G]GAAGCACCAGCCTTC	20844
rs387778054	in-del	-/TTCTTCTTC			intron-variant	Stam	GRCm38.p3	2:14079462	CTGTTCTTACATTCT[-/TTCTTCTTC]TTCTTCTTCTTCTTC	20844
rs578337509	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094507	AGAAGAAGGTATATC[C/T]TTTTGTTTTAGGATA	20844
rs578343740	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14089835	ATAAAGTTTTTTTAT[A/G]TTGTAGTGACCCCCC	20844
rs578346128	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14105392	CTTTTTGGCCCTGGC[A/G]TTCCCCTGTACTGGG	20844
rs578358313	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14095880	TTTCTATCGTCAGTG[G/T]TGCCTCACTTTGTGT	20844
rs578432816	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14093684	CCTGGGCTCTTTTTG[A/G]CTGGGAGACTATTAA	20844
rs578437949	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14098801	TTCAGAACTGTAAAA[C/T]GTATTATTGGGGTGT	20844
rs578505952	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14091417	TGTAAATGTACCACA[C/T]TTTCTGTATCTATTC	20844
rs578511878	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14134340	AAATTTAATTTTTAT[G/T]TATTTTTTTCAGTTA	20844
rs578516221	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095316	TAGTAGCCTGGGTTG[C/T]TCTTTGTGTTCTCTT	20844
rs578553142	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077921	GTGGACTAAGAAGAG[A/G]GCAAAGGCAGAACCT	20844
rs578562766	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14086994	GGACCTCCCCTTGAG[C/G]TGGATCCCATTTTGG	20844
rs578620011	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14105353	CCATACCCTCCCCCC[C/T]AATCCCCTACCCACC	20844
rs578632945	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14094390	TTAATCCATGGTGAT[C/G]TGATAGGATGCATGG	20844
rs578868852	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14094306	CCAAGGTATCTTTGA[C/G]AATAGCGTTGTTCAG	20844
rs578931567	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077690	AATTTGGTGAATGAG[A/G]GAAGTTTGACCACGT	20844
rs578932945	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14096679	CAAGCCTGAAACGGG[A/G]TCTGCCTCCGAAGCT	20844
rs578966762	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14093582	GGTAGAGTACTTTCT[G/T]CTTCTATTTTGTGGA	20844
rs579120664	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14102942	AAAACAACTACGATG[A/G]CCTTAACGTGGCCTT	20844
rs579127151	snp	A/G			upstream-variant-2KB, intron-variant	Stam, Stamos	GRCm38.p3	2:14072458	AGAATTTTTTCACAT[A/G]TATTTGAAGGCTTTT	20844
rs579132987	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095909	GTTTTCTTTATTGTG[C/T]CTACTTCCCTTTTTA	20844
rs579136691	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14092298	GTTGAAAATGTTGTC[G/T]TTTTTCCACTGGATG	20844
rs579153655	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14079031	AGGCTGGGCAGTGGT[A/G]GTGCACGCCTTTAAT	20844
rs579159556	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077654	TACTGCCGAGAACTG[A/G]CAAGGATTTGTTATT	20844
rs579173085	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14091591	GTAGTACTATGTCCA[C/G]TTTTCTGAGGAACCG	20844
rs579173808	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14093385	CCTGCATCCCTGGAA[C/T]GAAACCTACTTGGTC	20844
rs579214807	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14096360	GAGACTAGATCTCTC[C/T]TGAGTTTCAGTGGTC	20844
rs579227734	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095369	AGGCTCTTCTGGCTT[C/T]CATAGTCTCTGGTGA	20844
rs579476731	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14077339	CTTGTTCAAGCTGCA[C/G]GGTGATACCTAAATA	20844
rs579517697	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14096133	ATATGTTTTTAAATC[C/T]GGGTCTGTCTTTTCG	20844
rs579554637	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14117649	AGGTGACCCCCCCCC[A/C]CACACACACACACAC	20844
rs579576411	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14092692	ACATCTTTCCATCTC[C/T]TGAGATCTTCTTTAA	20844
rs579576701	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14094919	TGAGGTAGTATCTGT[C/G]TTTTTCCCTGAGATG	20844
rs579583114	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14140070	GGGGGGAGAAGGAGG[A/G]TGAAAGGGGAGAGTA	20844
rs579585961	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095520	ATTTCTTTTCTGTTC[C/T]AGTCTATTTGGAGTT	20844
rs579604628	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14091749	GGTGTGAGGTGGAAT[C/T]TCAGGGTTGTTTTGA	20844
rs579745857	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14094750	TATTCAGAATTGAGA[A/G]TTCCTCTTGGAAGAT	20844
rs579757762	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14090903	TCCTCCATTGGGGGC[A/C]CTGTGATCCATCCAA	20844
rs579763921	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14096019	GGTTGTGTTTTCCAG[G/T]TTTTCTTTAAGAACT	20844
rs579774779	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14077139	TTCTTTCTTTTTTTT[A/T]AAATTTTATTTTATT	20844
rs579794581	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14092404	TGGTCTACTTGTCTG[C/T]CTCTATACCAGTACC	20844
rs579898044	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14112006	GGTGGGCAACCAGGT[G/T]GAAGACAGGAGATTA	20844
rs580027201	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14095517	GGAATTTCTTTTCTG[G/T]TCCAGTCTATTTGGA	20844
rs580082362	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14078728	GGGGAAGGATGACAA[C/T]GGCACGTGGGGGCGG	20844
rs580123629	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14094627	TGTCCATTGATGAAA[A/G]TGGTGTGTTGAAGTC	20844
rs580123937	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14091688	TTCTCCACATCCTCG[A/C]CAGCATCTGCTGACA	20844
rs580124453	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14139760	CTCTGGCCTGGGGGC[A/G]AAGGGAAAGGGGTAG	20844
rs580131067	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094035	AGTTCTTCTTGTTTC[C/T]ACTTGGTTGATTTCA	20844
rs580157533	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14090761	CTCTTTCCAGTGATG[A/G]CCGACTAGTCCATCT	20844
rs580163604	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14108050	ACATGTTTATTTTTT[A/T]TATACTTCCACATCA	20844
rs580213579	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14099858	AATAAAAAGTCATAA[C/T]AAACAATGTATAGTT	20844
rs580227763	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14092778	TAGAGTCATGCCAAG[A/G]TATTTTATATTATTT	20844
rs580235942	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14096191	AAGGTGGGAGTACTG[A/G]GTTCTGATGATGGTG	20844
rs580258287	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14077404	GATTTTAAGCTCTGT[C/T]CTTCCAAGGACAATG	20844
rs580280362	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14091855	AGAATTCTTTGTTTA[C/G]CTCTAAGCCCCATTT	20844
rs580415158	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14093925	TTGTTAATTAGGATG[C/T]TGTCCCTGTGCCCTT	20844
rs580439690	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14078137	GAGGAAGAGGAGAGA[A/G]CTTGGAGCTCCCCTG	20844
rs580481475	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14140826	TTAGGAAGTTAGTGT[A/G]TTCTCTGTGTGTGTG	20844
rs580515549	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095623	AAGATATTTGCTGGC[C/T]CTTTAAGTTGAAAAT	20844
rs580625439	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077592	CCTACATTAGCCACA[A/G]CAGCCTCCTCATGAC	20844
rs580633456	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14096313	GAGCTTGTTTTTCTG[A/G]TGATTCTGTTAGCTT	20844
rs580669964	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14094169	TCTTTTTGGAGGCAG[A/T]CAGAGCTATGAGTTT	20844
rs580700496	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14093281	GTCAAATGCTTTCTC[A/T]GCATCTAACGAGATG	20844
rs580720159	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14078747	ACGTGGGGGCGGGGC[A/G]GGAAGTGGGTGAAAG	20844
rs580765704	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14090960	TGTTTGCTAGGCCCC[G/T]GCATAGTCTCTCAAG	20844
rs580779004	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14100059	ATTGCTTTCCAAAGA[C/T]GAAGTAATGTTAGAC	20844
rs580878443	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14092071	CCATTCTCCATCTTA[C/G]AGCACAAGCCATTGC	20844
rs580892849	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095874	CTAGGGTTTCTATCG[C/T]CAGTGGTGCCTCACT	20844
rs581039789	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14126655	GTATCTTGGTTAGCT[A/T]ATGGCTCTCAACGGT	20844
rs581041176	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14093185	TACTGGTTTGCTGTA[G/T]ATTGCTTTTATCATG	20844
rs581108751	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14103940	GATGAATGTTTAGCT[G/T]TAATTGTTACCTTGG	20844
rs581111824	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14077496	AGGACGAGGCAGGCA[A/C]ATCTCTGAGTTCAAG	20844
rs581184448	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14095299	GAGAGTTTGGCCGGG[G/T]ATAGTAGCCTGGGTT	20844
rs581187656	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094312	TATCTTTGAGAATAG[C/T]GTTGTTCAGTTTCCA	20844
rs581190856	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14091295	TATATCATGTGAGTT[C/T]TTTTATGATAGGGCT	20844
rs581192577	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14077666	CTGACAAGGATTTGT[A/T]ATTTGGAAAATTTGG	20844
rs581207911	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14079164	AAAAAAAAAAACAAA[C/T]AAAATAAACAAACAA	20844
rs581213160	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14096284	GAGTTAGTTGTTATA[C/G]TTGTTTCTAGTTAGA	20844
rs581283054	snp	G/T			downstream-variant-500B	Stam	GRCm38.p3	2:14149430	TGTTTTTTTTACTTA[G/T]TACCTTGTTTACTTA	20844
rs581287758	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14095208	TATTATCCTTTGAAG[G/T]GCTGGATTCATGGAA	20844
rs581317968	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14099956	TAGATGTATTCACAT[A/G]GGCTTTTTTTTTTTT	20844
rs581319861	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14091088	CAGTCTCTAGATGGT[C/G]CATCCTTTTGTCTCA	20844
rs581372565	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14125483	GCATTTTCTATACCT[C/G]TTCTAGAACTTGTTA	20844
rs581390331	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095682	TAGGTTTGGTCTTCT[C/T]ATTGTGTCCTGGATT	20844
rs581394709	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14091986	TCCCAATCTGTTGGT[A/G]GCCTTTTTGTCTTAT	20844
rs581399365	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14096382	TCAGTGGTCAGAGCA[C/G]TCTCTGTAGGCAAGC	20844
rs581421848	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14093433	TGATGTGTTCTTGGA[A/T]TCAGTTAGCGAGAAT	20844
rs581659560	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14098802	TCAGAACTGTAAAAT[A/G]TATTATTGGGGTGTT	20844
rs581752255	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14093734	AGGGGATATAGGACT[A/G]TGTAGATCATTAACC	20844
rs581763689	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14094301	GTTGACCAAGGTATC[A/T]TTGAGAATAGCGTTG	20844
rs581772490	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14078872	CCCAGAGTAACGCGA[C/T]CTGCTATAGAGGAAA	20844
rs581818658	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14094442	ACTGTTGAGGCCTGT[G/T]TTGTGACCAATTATA	20844
rs581831668	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077312	ATAAACCAGAGCCTG[A/G]AAAAGTAGAAACTTG	20844
rs581880566	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14091520	GCATGTGTCCTTATT[A/G]CAAGTTGAAACATCT	20844
rs581886432	snp	A/G			intron-variant, downstream-variant-500B	Stam	GRCm38.p3	2:14138354	TGGTGGGGCGTGCCT[A/G]TAAACCCAGCACAGT	20844
rs581886470	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077943	GCAGAACCTTGGCAC[A/G]CAACACTTAAAACGA	20844
rs581888667	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095318	GTAGCCTGGGTTGTT[C/T]TTTGTGTTCTCTTAG	20844
rs581941299	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14092518	AGAGTTTTTGCTATC[C/T]TAGGTTTTTTGTTAT	20844
rs581949363	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14105358	CCCTCCCCCCTAATC[C/T]CCTACCCACCCACTC	20844
rs582061660	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14087547	ACCATACATGGGTCT[A/G]AGTTGCCTCATTCAG	20844
rs582148090	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14093660	AACTCTGCACTAAAT[C/T]CATCTGATCCTGGGC	20844
rs582210305	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14096031	CAGTTTTTCTTTAAG[A/G]ACTTGTAACTCTTTA	20844
rs582262479	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14111723	TAGTTTTCTCTTCTG[C/T]GGAGTGGGCCTCAGA	20844
rs582326514	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14096701	TCCGAAGCTGTGTGG[C/T]TTCTGCCTGTCCCAG	20844
rs582372149	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14139769	GGGGGCAAAGGGAAA[A/G]GGGTAGGAGGAGAGC	20844
rs582393477	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095437	GTTACTTGACCTTTT[C/T]CCCTTACTGCTTTTA	20844
rs582409109	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14091701	CGACAGCATCTGCTG[A/T]CACCTGAATTTTTGA	20844
rs582416993	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14095941	ATCTAGTATGGTTTT[G/T]TTCATTTCCATCATC	20844
rs582435335	snp	C/T			intron-variant, upstream-variant-2KB	Stam, Stamos	GRCm38.p3	2:14075687	GAACCCAGGGCCTAA[C/T]ATGTATTCTTTCTGT	20844
rs582446997	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14092344	TCAAAGATCAAATGA[C/T]CATAGATGTGTGGGT	20844
rs582529028	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14091593	AGTACTATGTCCACT[C/T]TTCTGAGGAACCGCC	20844
rs582716383	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14092130	GCCCATATCTTCAAG[A/G]CTTTTCCCCACTTTC	20844
rs582735958	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14139117	CTTCCCAGGTCGGTT[C/T]TGTAAAGGTCAGGGT	20844
rs582784978	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14091814	TTTTTTCAGGTGCTT[C/T]TCAGCCATTAGGTAT	20844
rs582858715	snp	A/G			intron-variant, upstream-variant-2KB	Stamos, Stam	GRCm38.p3	2:14071985	GTTAATGTTATCCAT[A/G]CTAATATATGTTATT	20844
rs582861660	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095890	CAGTGGTGCCTCACT[C/T]TGTGTTTTCTTTATT	20844
rs582994456	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14094535	ATAAAATGTTCTGTA[A/G]ATATCTGTTAAATCC	20844
rs583002455	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14107819	ATGATTTTTTGGCTC[C/T]AGCTCCAGTGTATGA	20844
rs583062055	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14078777	GCCATAACTGATAGC[A/T]GGAGAGAAAACCCTG	20844
rs583064035	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14140071	GGGGGAGAAGGAGGG[C/T]GAAAGGGGAGAGTAA	20844
rs583072031	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14095549	TTCTGTAGACATCTT[G/T]TATGTTCATGGGCAT	20844
rs583074166	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094170	CTTTTTGGAGGCAGT[C/T]AGAGCTATGAGTTTT	20844
rs583134218	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14096308	AGTTAGAGCTTGTTT[C/T]TCTGGTGATTCTGTT	20844
rs583302608	snp	A/G/T			intron-variant	Stam	GRCm38.p3	2:14093210	ATCATGTTTAGGTAT[A/G/T]GGCCTTGAATTCCTG	20844
rs583306415	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14112008	TGGGCAACCAGGTGG[A/G]AGACAGGAGATTATA	20844
rs583323329	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14094050	CACTTGGTTGATTTC[A/G]CCCCTGAATTTGATT	20844
rs583344588	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14090764	TTTCCAGTGATGGCC[A/G]ACTAGTCCATCTTTT	20844
rs583416404	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094874	TCTTCATACCATTTG[C/T]TTGGAAAATTGTTTT	20844
rs583422916	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14090942	TGTGAGCATCCACTT[A/C]TGTGTTTGCTAGGCC	20844
rs583495000	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14078733	AGGATGACAATGGCA[C/T]GTGGGGGCGGGGCAG	20844
rs583501759	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14099899	AGGTCTATTAGTTCT[A/G]GTTAGCATGAAACTT	20844
rs583542001	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094711	CTTTAATGAATGTGG[C/T]TGCCTTTGCATTTGT	20844
rs583595352	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14077408	TTAAGCTCTGTTCTT[A/C]CAAGGACAATGTCAA	20844
rs583646732	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14092954	GTGGAATTTTTGGTG[C/T]CACTTATATATACTA	20844
rs583660775	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14096210	CTGATGATGGTGAGT[G/T]GTCTTGGTTTCTGTT	20844
rs583691792	snp	A/C/T			intron-variant	Stam	GRCm38.p3	2:14095664	ATCTACTCCTATTAT[A/C/T]GGTAGGTTTGGTCTT	20844
rs583870424	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14092726	CTTTTTTCAGAGACT[C/G]GAAGTTCTTATCATA	20844
rs583901390	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14143953	TACATACACATTACA[C/T]ACGTGCGTGTGTATG	20844
rs583911809	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14091860	TCTTTGTTTAGCTCT[A/G]AGCCCCATTTTTTAA	20844
rs583939396	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14092117	TTTTTTCCCCTGTGC[A/C]CATATCTTCAAGACT	20844
rs583980233	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14093929	TAATTAGGATGCTGT[C/T]CCTGTGCCCTTTAAT	20844
rs583984294	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14078552	ACGTGAGTTACTGGT[A/G]GTCTGAAAGATGGAT	20844
rs583992072	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14099358	TCTGGGCTGGTAGTC[A/T]TGGTTCTATAAGAGA	20844
rs584065541	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14096162	CGGGTGTGTTGGGGT[A/G]CCCAGGACTGGCTAA	20844
rs584079149	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095018	TTGGGGAATTGAGTC[C/T]ATTGATATTCAGAAA	20844
rs584094110	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077343	TTCAAGCTGCACGGT[A/G]ATACCTAAATACATG	20844
rs584151770	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095878	GGTTTCTATCGTCAG[C/T]GGTGCCTCACTTTGT	20844
rs584182022	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14090971	CCCCGGCATAGTCTC[A/T]CAAGAGACAGCTATA	20844
rs584256233	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077548	GATTATTGACATCTA[A/G]TTGATGGCAGCCAGG	20844
rs584328858	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14094313	ATCTTTGAGAATAGC[A/G]TTGTTCAGTTTCCAC	20844
rs584515527	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14126649	TGATAAGTATCTTGG[C/T]TAGCTAATGGCTCTC	20844
rs584527379	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14091201	CTTCGTTCTTCTTGA[G/T]TTTCATGTATTTTCC	20844
rs584542387	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14104437	TGGGGTTCCAGTGAA[C/T]GTTGGTGGTTTTAAC	20844
rs584571545	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14079169	AAAAAACAAACAAAA[C/T]AAACAAACAAAAAGT	20844
rs584602405	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14087553	CATGGGTCTGAGTTG[C/G]CTCATTCAGGATATT	20844
rs584613319	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095313	GTATAGTAGCCTGGG[C/T]TGTTCTTTGTGTTCT	20844
rs584619203	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14091309	TTTTTTATGATAGGG[C/T]TACCTCACTCAGGAT	20844
rs584619403	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14127709	AATCCTTGTTTAAGT[A/T]CCAGAGATTAACAAG	20844
rs584654433	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14092018	GACAGTGTCTTTTGC[C/G]TTACAGATGCTTTGC	20844
rs584669201	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14095719	ATGTTTTAAGTTACG[A/T]TCTTTTTCCATTTTG	20844
rs584730812	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14095277	GGTTTCTCCATCTAT[C/G]GTAATTGAGAGTTTG	20844
rs584851530	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14093512	GTTCTCTATCTTTGT[C/T]GGGTCTTTCTGTTGT	20844
rs584856607	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14077683	TTTGGAAAATTTGGT[G/T]AATGAGGGAAGTTTG	20844
rs584869546	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14095893	TGGTGCCTCACTTTG[A/T]GTTTTCTTTATTGTG	20844
rs584905810	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14093317	GTGGTTTTTGTCTTT[G/T]AGTTTGTTTATATAG	20844
rs585052385	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14096443	CTGGAGTTTGGACCT[C/G]CCTCCTGGCAGAAGA	20844
rs585140616	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14092246	GATCAATTCGCATTC[C/T]TCTACATGATAACCA	20844
rs585144595	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14091547	ATCTTCTGGGTATAT[A/G]CCCAGGAGAGGTATT	20844
rs585146318	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14096320	TTTTTCTGGTGATTC[A/T]GTTAGCTTCTATCAG	20844
rs585196726	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14078991	ATAACTCATGATAAA[G/T]TATGTTAATCAAGAG	20844
rs585222089	snp	C/T			intron-variant, downstream-variant-500B	Stam	GRCm38.p3	2:14138372	AACCCAGCACAGTGC[C/T]GTGGCTAGGGAGAAG	20844
rs585230013	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095325	GGGTTGTTCTTTGTG[C/T]TCTCTTAGTGTCTGT	20844
rs585236919	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14102937	TGAGAAAAACAACTA[C/T]GATGGCCTTAACGTG	20844
rs585240340	snp	A/C			upstream-variant-2KB, intron-variant	Stam, Stamos	GRCm38.p3	2:14072299	TCATAATGACACAAA[A/C]GCACTTCAAAAATCT	20844
rs585247734	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14092613	GATTGCATTGAATCT[C/G]TAGATTGCTTTTGGC	20844
rs585270674	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077646	TCTCTCTCTACTGCC[A/G]AGAACTGACAAGGAT	20844
rs585389132	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14098794	TTATTAGTTCAGAAC[C/T]GTAAAATGTATTATT	20844
rs585413655	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077721	GAGCTGAGATACAAA[A/G]GTTTAGGGGCAGGAC	20844
rs585485620	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094716	ATGAATGTGGTTGCC[C/T]TTGCATTTGTAGCAT	20844
rs585515835	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14096061	AGCAGTGTTCTCCTG[C/T]ATTTCTTTAAGTGAG	20844
rs585551390	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077314	AAACCAGAGCCTGAA[A/G]AAGTAGAAACTTGTT	20844
rs585594272	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094450	GGCCTGTGTTGTGAC[C/T]AATTATATGCACAAT	20844
rs585606027	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14105364	CCCCTAATCCCCTAC[A/C]CACCCACTCCCCCTT	20844
rs585708531	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14093676	CATCTGATCCTGGGC[A/T]CTTTTTGACTGGGAG	20844
rs585732537	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14139786	GGTAGGAGGAGAGCT[C/T]TGGCCGGTTATCTCA	20844
rs585738431	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095519	AATTTCTTTTCTGTT[C/T]CAGTCTATTTGGAGT	20844
rs585774444	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14139122	CAGGTCGGTTCTGTA[A/G]AGGTCAGGGTGTTGA	20844
rs585786296	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14091641	GGTTGTACAAGCTTG[C/T]AATCCCACCAACAAT	20844
rs585794688	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14090889	GTACTTTCTCTAGCT[C/G]CTCCATTGGGGGCAC	20844
rs585838663	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14091744	TGACTGGTGTGAGGT[A/G]GAATTTCAGGGTTGT	20844
rs585858560	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14096176	TACCCAGGACTGGCT[A/G]AGGTGGGAGTACTGG	20844
rs585863317	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14077091	CTAAGAGTCATGTTC[G/T]TTCTTTCTTTCTTTC	20844
rs585873376	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14092371	GGGTTCATTTCTGGG[G/T]CTTCAATTCTATTCC	20844
rs585920598	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095985	TTTCCTGTTTTTCTT[C/T]AAGGACTTCTACCTG	20844
rs585949822	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14090700	CTTCTTGGCCCTGGC[A/G]TTCCCCTGTACTGAG	20844
rs586137146	snp	A/C			intron-variant	Stam	GRCm38.p3	2:14095466	TAATATTCTATCTTT[A/C]TTTAGTGCATTTGTT	20844
rs586164710	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14094013	TGGTTTGGTTGATTC[G/T]TTGAATAGTTCTTCT	20844
rs586170800	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14078660	CAGTTTAAGGATGGG[C/T]TGTTGCCCAGAAGAA	20844
rs586174819	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14099470	GCTTGAGTTCCAGTC[C/T]TGACTTCCTTTGGTG	20844
rs586350412	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14108039	CTCTGGGAGGGACAT[G/T]TTTATTTTTTTTATA	20844
rs586354421	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14094607	TAGTTTCTGTTTCCA[G/T]GATCTGTCCATTGAT	20844
rs586380950	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14078042	AATAGTAAGAAAGAA[A/G]AAAGGAAGGGAGAAA	20844
rs586403049	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14093278	TTTGTCAAATGCTTT[C/T]TCAGCATCTAACGAG	20844
rs586405475	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14099313	CAATTAGTGATCAAG[A/G]GGGGAGGTCCCCTTG	20844
rs586425767	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14093890	GATCTGTTGTTATGT[C/T]TCCTTTTTCATTTCT	20844
rs586432991	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14078742	ATGGCACGTGGGGGC[A/G]GGGCAGGAAGTGGGT	20844
rs586773316	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14095280	TTCTCCATCTATGGT[A/G]ATTGAGAGTTTGGCC	20844
rs586781110	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077558	ATCTAGTTGATGGCA[A/G]CCAGGATGCTATTTG	20844
rs586786786	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14096312	AGAGCTTGTTTTTCT[C/G]GTGATTCTGTTAGCT	20844
rs586795205	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14092041	TGCTTTGCAATTTTA[G/T]GAAGTCCCACTTGTC	20844
rs586804299	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095762	TATTTGATTGTTGTG[C/T]TGATGTTCTCTATGG	20844
rs586824290	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14094075	TTGATTATTTCCTGC[C/T]GTCTACTCCTCTTAG	20844
rs586847501	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14094913	TCATTCTGAGGTAGT[A/G]TCTGTGTTTTTCCCT	20844
rs586853509	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14090959	GTGTTTGCTAGGCCC[C/T]GGCATAGTCTCTCAA	20844
rs586893651	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14112016	CAGGTGGAAGACAGG[A/G]GATTATATTGCTTTG	20844
rs586945050	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14091981	TCCTTTCCCAATCTG[A/T]TGGTGGCCTTTTTGT	20844
rs586947276	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14143956	ATACACATTACACAC[A/G]TGCGTGTGTATGTGT	20844
rs586972759	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14093136	ATTTTAGTGGGATTG[C/T]TTCCAGCTTCTCACC	20844
rs586986199	snp	C/G/T			intron-variant	Stam	GRCm38.p3	2:14096211	TGATGATGGTGAGTG[C/G/T]TCTTGGTTTCTGTTA	20844
rs586987687	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14090977	CATAGTCTCTCAAGA[C/G]ACAGCTATATCAGGG	20844
rs586989692	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14091280	ACATATCAGTGAGTA[C/T]ATATCATGTGAGTTT	20844
rs586999385	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14077472	ATGTCTTTAATCCCA[A/G]CACTCAGGAGGACGA	20844
rs587152706	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14095591	GGTTTGGGTAGTTTT[C/T]TTCTATAATTTTGTT	20844
rs587198183	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14126654	AGTATCTTGGTTAGC[C/T]AATGGCTCTCAACGG	20844
rs587339557	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14092767	ACTTCCTTAGTTAGA[A/G]TCATGCCAAGGTATT	20844
rs587343225	snp	A/G			intron-variant	Stam	GRCm38.p3	2:14095665	TCTACTCCTATTATT[A/G]GTAGGTTTGGTCTTC	20844
rs587359177	snp	C/G			intron-variant	Stam	GRCm38.p3	2:14095108	TCTTGTGGCTGTCTT[C/G]TTTTAGGTTTGTTGA	20844
rs587413351	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14077374	CCTTTAATCTAGTGA[C/T]TTTCAATCCTAGTAG	20844
rs587451540	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14125461	CTGTGCCACAAACCT[C/T]AGAATTGCATTTTCT	20844
rs587517057	snp	G/T			intron-variant	Stam	GRCm38.p3	2:14091825	GCTTCTCAGCCATTA[G/T]GTATTCCTCAGGTGA	20844
rs587566204	snp	C/T			intron-variant	Stam	GRCm38.p3	2:14078869	AATCCCAGAGTAACG[C/T]GACCTGCTATAGAGG	20844
rs587569345	snp	A/T			intron-variant	Stam	GRCm38.p3	2:14094255	TTTCATTAAACTCTA[A/T]AAAGTCTTTAATTTC	20844
rs864293639	snp	A/G/T			intron-variant	Stam	GRCm38.p3	2:14091210	TCTTGAGTTTCATGT[A/G/T]TTTTCCAAATTGTAA	20844
rs864307635	snp	C/G/T			intron-variant	Stam	GRCm38.p3	2:14090841	CATAATGTTGTTCCA[C/G/T]CTATAGGGTTGCAGA	20844

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