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

Fchsd2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3656411	snp	A/G	0.42344	0.180051	intron-variant	Fchsd2	GRCm38.p3	7:101222804	TTCCATTTTTGTCTA[A/G]ATTCCTCTGTTCTGT	207278
rs3657035	snp	A/C	0.362812	0.2231	intron-variant	Fchsd2	GRCm38.p3	7:101222906	GAAAATAAACATAGA[A/C]ACCTAATCTCAAACC	207278
rs3674231	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101179628	CTTCCTTTTCCCTCT[C/T]CAAATCTTCCCGTAC	207278
rs3674798	snp	C/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101179704	TATTGCTACATATGT[C/G]TATGTGTGTATGCAT	207278
rs3679370	snp	C/T	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101217715	AGCCATCTCTCTAGC[C/T]CCAGTATTAATATTT	207278
rs6155955	snp	A/G	0.48	0.0979796	intron-variant	Fchsd2	GRCm38.p3	7:101275245	GTATTTTTGTGTATG[A/G]TATTGTGTTCCTATT	207278
rs6156378	snp	A/T	0.48	0.0979796	intron-variant	Fchsd2	GRCm38.p3	7:101275260	GTATTGTGTTCCTAT[A/T]GAAAGGATGGCCCTT	207278
rs6245271	snp	A/T	0.415225	0.187619	intron-variant	Fchsd2	Mm_Celera	7:101133405	GCACTGAATGACAGG[A/T]TTTTGAGGTGAACAA	207278
rs6250697	snp	A/G	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101214400	caaagagtacacacc[A/G]gggacccatggctcc	207278
rs6251625	snp	A/G	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101214561	aggagctccctcata[A/G]aggcagggggatggg	207278
rs6251648	snp	A/G	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101214581	agggggatgggggag[A/G]ggataggggtttgtg	207278
rs6252140	snp	C/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101214684	TAAAAGGGCTTTTTA[C/T]AGCATACCAGCCTAT	207278
rs6284925	snp	C/T	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101222781	TTCCTCTGCAGAAAA[C/T]ATTAAATTTCCATTT	207278
rs13474820	snp	A/T			utr-variant-3-prime	Fchsd2	Mm_Celera	7:101284229	AAAATATGCCTCCtt[A/T]ttaaaaataaataaa	207278
rs13479429	snp	C/T	0.464806	0.127899	intron-variant	Fchsd2	Mm_Celera	7:101171025	TTTTTCCCCTGATGC[C/T]AGAACAGAACCTAGG	207278
rs31046427	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101274748	AGAAAGAGCATTGTG[C/T]GCTCAGAGAACAGGA	207278
rs31046740	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101255665	AGTATCTGTAAAATT[C/G]TCTTCAAATGAGCTC	207278
rs31049794	snp	C/T	0.48	0.0979796	intron-variant	Fchsd2	GRCm38.p3	7:101228338	AACGACATGTTTTTT[C/T]CTCCTAATTCCTAGC	207278
rs31052011	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101282066	GATCACAAGTGTGTG[C/T]CACCCTGCCTGACTA	207278
rs31053090	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101275283	TGGCCCTTTGTAGTC[A/C]AGGCTAGCCTAGAAT	207278
rs31055185	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101238411	TTTCCCGGGCGGCGA[C/G]CGGGAATCCCTGTGA	207278
rs31056013	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101218378	TATGCAGCTGGAGCC[A/T]TGAGTCCCACCATGT	207278
rs31058533	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101136905	GTGTATGTGGAGGTC[A/G]AAGGACAACTTATGA	207278
rs31078157	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101230348	CAATAACCAAAAGAA[A/G]GACAGGCAAGCGTCA	207278
rs31080605	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101166911	AACAGCCAGGATGGT[A/C]CAGCCCACTATAAAA	207278
rs31085924	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101248528	GGTGAGTCTCTGTAA[A/C]TGGAACGCCTAGTCA	207278
rs31089870	snp	A/G	0.432133	0.171253	intron-variant	Fchsd2	Mm_Celera	7:101134634	TGATCATATCTTCTC[A/G]TGTGCTAAGTAGAGC	207278
rs31089872	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101219600	GGTGTTGCTGCCACA[C/T]CCAGCCATGATCTTA	207278
rs31089966	snp	C/T	0.444444	0.157135	synonymous-codon	Fchsd2	GRCm38.p3	7:101198522	TACCAAAGCTACCCA[C/T]GCAAGGAATGATTAC	207278
rs31090529	snp	G/T	0.304688	0.243945	intron-variant	Fchsd2	GRCm38.p3	7:101128545	CTAGTTCATGCGTTT[G/T]AAATTAATGATTTGT	207278
rs31092837	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101111675	CAAAAAAATCAAAAA[C/T]CCAAAGGTACTGTAA	207278
rs31099485	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101264114	GGGATTAAAAGCATG[C/T]TCCACCACCGCCTAG	207278
rs31103422	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101157650	TGGTATATTAAAAAA[A/T]TATTTTTTCTTTTTT	207278
rs31114260	snp	C/T	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101271849	TGAAATATTGAGTCT[C/T]TGCTGTCTGACTTTT	207278
rs31147670	snp	C/T	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101260007	TGGGCTATTGGTGTC[C/T]GTCCCCCAAACTTAT	207278
rs31148162	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101119228	ATTGGCCCAGGGACT[C/T]CCTGTGTGGCTGAAG	207278
rs31148715	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101248716	TAGTAATATGCCTAG[A/G]GTTAGTGGGTCATAC	207278
rs31149587	snp	C/T	0.415225	0.187619	intron-variant	Fchsd2	GRCm38.p3	7:101121845	TCTAGTCTTCACATG[C/T]GTGTGTGTTCATGTA	207278
rs31151822	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101224621	TAGAGCTTTCAGATG[C/T]AATTTTAAATTGTTG	207278
rs31151957	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101229335	AATAATTAAAAATAA[A/T]TTTTAAGAATAGTTT	207278
rs31152316	snp	A/G	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101222043	CAAAGATGTAGACAA[A/G]AAGAGCCTGCGGTAG	207278
rs31157140	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101266258	AATTGGCTCTTTTAT[A/G]ATTTTTTTTTTTCTT	207278
rs31160494	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101157652	GTATATTAAAAAAAT[A/T]TTTTTTCTTTTTTTT	207278
rs31182268	snp	C/T	0.359862	0.224567	intron-variant	Fchsd2	GRCm38.p3	7:101228162	CTATTTTAGAAATGT[C/T]CAGTGGTCTCAGAAA	207278
rs31183078	snp	G/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101269415	GGTTCATGTAGCCCA[G/T]ACTGGCCTGAACTCA	207278
rs31185067	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101139033	TCATAAAGAGGAATA[C/T]ACCCCCCTCCATATA	207278
rs31185770	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101242572	GTATATTGACGCCTA[C/T]TTGATTATGATGGAT	207278
rs31186959	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101275950	TGAGTTTCCTCCAGG[C/T]TCTGAGTCTCAGAAG	207278
rs31194822	snp	A/G	0.231111	0.249285	intron-variant	Fchsd2	Mm_Celera	7:101224475	TGTTGACTTTCTCAA[A/G]GAACCAGCTCTTGGT	207278
rs31196188	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101171411	TAGAATTAAAGTTAT[C/T]CACTACCATGCCATG	207278
rs31196675	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101238910	GCCGCTGACCAGTCC[A/G]CTACCTCTCCAGCTG	207278
rs31198525	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101110126	GAAATCCCAGGGTCC[G/T]GCCTGGCGAGGATGG	207278
rs31200488	snp	C/G	0.375	0.216506	upstream-variant-2KB	Fchsd2	Mm_Celera	7:101107253	TCACACTGTGGCTGC[C/G]TGTGGAGCTGTGGCT	207278
rs31200746	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101266948	CACACTGTCCTCAGC[C/T]TGGAAACTTCTTCTG	207278
rs31201734	snp	C/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101155369	TTCATACGTGTACTC[C/G]CAGCCCTCAGTAGGC	207278
rs31202802	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101210440	TTCAATATCTTTCCT[A/G]TGTTCCCTTGAATCC	207278
rs31211060	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101239513	GCCATGTCTTTTTAA[A/C]AACAAAAACCCCTGG	207278
rs31212386	snp	A/C	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101220378	AGCCTTGTCTATATA[A/C]ATTTAAAAATATTAC	207278
rs31229229	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101206890	CTTGGTGGCTATAGG[C/T]TGGGGTAATTCTCAT	207278
rs31236875	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101261072	CCTATCTGTAAGCAC[A/T]CCATAGCATCAGTAA	207278
rs31240750	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101208215	GCCACTGGTCAGTAA[C/T]TTCTAACTCCTCTTT	207278
rs31244614	snp	A/G	0.456747	0.140554	intron-variant	Fchsd2	GRCm38.p3	7:101276322	TTTGGAGTACATGGA[A/G]GTATTATGCTGAATA	207278
rs31245262	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101266173	TGCTTTTTTGTTGTT[A/G]TTGTTTTCCTGTTTT	207278
rs31246396	snp	A/G	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101228149	CTTTTGCCCAGCACT[A/G]TTTTAGAAATGTCCA	207278
rs31251887	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101223653	AGTTCTCTGGCAGAG[G/T]TTTTGGGGCTACTTA	207278
rs31255913	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101162060	ATATATCCCTTGTCT[C/T]ACATGTACAGCTTTT	207278
rs31259501	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101129477	CAGGGGTAGTAATGT[C/T]CTTTTTATTGGGCAC	207278
rs31263421	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101167560	TTTGTATCTCCTCCC[A/G]TGGGTATTTTGTTCC	207278
rs31268927	snp	A/G	0.21875	0.248039	intron-variant	Fchsd2	GRCm38.p3	7:101117486	TTCCACAAGAAGAGC[A/G]AAGATGTGATTGTTT	207278
rs31269014	snp	A/G	0.493827	0.0552116	intron-variant	Fchsd2	GRCm38.p3	7:101116396	ACTATTACCTGCTAA[A/G]ACATGCTTTTAGGCC	207278
rs31280093	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101238412	TTCCCGGGCGGCGAG[C/T]GGGAATCCCTGTGAG	207278
rs31281962	snp	G/T	0.33241	0.236027	intron-variant	Fchsd2	GRCm38.p3	7:101129251	GGAGAAGGATTTGCT[G/T]AGCTTGGGGAACAGT	207278
rs31283923	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101272338	AACAACTAGAGCTCC[C/T]TTTGCCCTTACAGAG	207278
rs31287431	snp	A/G	0.277778	0.248452	intron-variant	Fchsd2	GRCm38.p3	7:101123825	CTGCTGGGCTGGATG[A/G]GTGACAGGGATCCAC	207278
rs31287968	snp	A/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101196647	GCCAGCAAACATGAA[A/T]AACTTATTGCAGGGG	207278
rs31297478	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101201824	TACAATGAGCAGATA[C/T]GTGACAGGGAGGTAG	207278
rs31299401	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101261415	CACACACCTCCCGAG[A/G]TTACCTGTGCCTGTT	207278
rs31301721	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101131768	CTGTCTCAGACGCCT[A/G]AGAGCTGGGGTTAGT	207278
rs31313002	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101153409	CATAAAACATATTTA[A/T]AAAAAAAACTAATTT	207278
rs31322659	snp	G/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101169409	AGGTTTTTGTTTTTT[G/T]GGGTTTTTTTTCTGA	207278
rs31323274	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101153410	ATAAAACATATTTAA[A/T]AAAAAAACTAATTTG	207278
rs31328813	snp	G/T	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101132485	ATAGTTCAATCTACT[G/T]TGGGAAAGTCTGAGC	207278
rs31338986	snp	C/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101219506	TGTGTAGCCTTAGCT[C/G]TCCTGGAATTCACTC	207278
rs31341364	snp	C/T	0.401235	0.199068	intron-variant	Fchsd2	Mm_Celera	7:101138968	TTGTTACTGCAACTG[C/T]TGTGAAAAACGGCAG	207278
rs31342117	snp	A/G	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101263665	AGTTGCACTAAGGCA[A/G]TCTGACAGTCTGCTT	207278
rs31343984	snp	A/C	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101190709	GTGATAAAGTATATG[A/C]ACAGTTACAAGGCCC	207278
rs31359195	snp	A/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101209136	ACAATGGCATGTTAA[A/T]TAGTTGTACCAAGAG	207278
rs31373111	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101224410	AATTTTGTTAGTTTG[A/G]ATACTGTCTCTCTGC	207278
rs31373592	snp	C/T	0.42	0.183303	intron-variant	Fchsd2	GRCm38.p3	7:101187991	TACCAAAGCCTCTCA[C/T]ATTTTCTCATTCTGG	207278
rs31376575	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101267707	CCGCTACAGAAACTC[A/C]CACAGGGTTCTTCTT	207278
rs31381535	snp	C/T	0.401235	0.199068	synonymous-codon	Fchsd2	GRCm38.p3	7:101276925	CAGTCTTTGGCTGCT[C/T]TGGACAGTCGGTCAC	207278
rs31383500	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101209300	TGGCTGGAAGCCCAC[A/T]AGTGATTGTCCAGTG	207278
rs31389068	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101228809	ACTTCTTGATCTTAC[A/G]GAGGACCCTGGCATG	207278
rs31396415	snp	G/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101209560	AAATTTGGTTTTTTT[G/T]GGGACAGTTTTTCTT	207278
rs31399591	snp	A/G	0.432133	0.171253	downstream-variant-500B	Fchsd2	GRCm38.p3	7:101284732	AACCTTTTACTCACT[A/G]AGCCATGGATGTGGA	207278
rs31405110	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101173930	AATTAATTAGTGTAG[A/G]TAATTTTCTTTGTAA	207278
rs31410606	snp	A/G/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101247326	TCTTGTATTGAAGCA[A/G/T]ATGTCATTTCAGCAA	207278
rs31411954	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101208253	TCTTGCCTGTTATTT[A/T]TTTGTCTGTATAAAT	207278
rs31423807	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101144857	TGTGTGTTTTATCAC[C/T]AGTGGATTTGCTGGC	207278
rs31424196	snp	A/G	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101258466	CATTCAAAGACTCCT[A/G]AACACAGTTAGGAGA	207278
rs31426717	snp	A/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101158279	CCACACTTTGTCTCC[A/G]TATTTCCTCCCATAA	207278
rs31426786	snp	A/G	0.375	0.216506	utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101283024	AATGCAACCTTATTG[A/G]GAAGAAAGTGGACTG	207278
rs31427765	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101128156	TAAAATTTGTGAAAC[A/T]GATTCTAAACTTAAG	207278
rs31428309	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101193901	AGACTCTTAAAGTGT[A/T]ACAGATAGGTGTCAG	207278
rs31429055	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101149450	TTTATTATTATTATT[A/G]TTGTTGTTGTTGTTG	207278
rs31429405	snp	C/T	0.345679	0.230967	intron-variant	Fchsd2	GRCm38.p3	7:101217167	AAATTAGGTGTAATT[C/T]TAGTAATAACTCGAT	207278
rs31438719	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101224405	TTTCTAATTTTGTTA[A/G]TTTGGATACTGTCTC	207278
rs31441591	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101209849	TGGCCCTTGCTGTCA[A/T]GGAACTCACTCTAGA	207278
rs31449204	snp	A/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101246145	AAAGTTAGAATAGTA[A/G]TGACTCTTACCTCAC	207278
rs31461996	snp	A/G	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101191877	TTTGTTCTCTCTTAA[A/G]GAAGGTCTGGCCTCA	207278
rs31472558	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101182206	TCACATAATGTCTGG[C/T]TGTGTGTCTCTGCAT	207278
rs31476415	snp	G/T	0.498615	0.0262793	intron-variant	Fchsd2	GRCm38.p3	7:101163924	ATTTCTCATGAAATT[G/T]CAAGGACATAAGTTG	207278
rs31477948	snp	A/G	0.345679	0.230967	intron-variant	Fchsd2	GRCm38.p3	7:101119404	TTTTATGCTACATGC[A/G]GCAGGTCCCACCATA	207278
rs31481207	snp	A/T	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101130401	CTCCCCAGGACTTGG[A/T]TTTTTACATGAGTAC	207278
rs31482565	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101248532	AGTCTCTGTAAATGG[A/T]ACGCCTAGTCAGCCT	207278
rs31487934	snp	C/T	0.33241	0.236027	intron-variant	Fchsd2	GRCm38.p3	7:101194498	TTTAATCACAGGTAA[C/T]TCAAAAGAAATAAAG	207278
rs31496879	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101266605	TTCTGCTGCTCTTGA[A/G]TGCTGTGTTCTACAA	207278
rs31501171	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101278947	TGGATATGGATGGGA[A/C]GAGGGAATGGGTAGA	207278
rs31501591	snp	C/T	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101268365	CTGAAATGTTAATAC[C/T]CAAGAGAAAAGCCAT	207278
rs31508881	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101224340	CAGGCTTTTGAAGCA[C/T]GATCTAATGATTCTT	207278
rs31514841	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101174812	CGCCACTGCTCCTGG[C/G]TCTTTTCCCTTCTCT	207278
rs31516731	snp	C/T	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101234112	TCTGAAAAAAATTCT[C/T]CTTAACAAAGTGAGA	207278
rs31517243	snp	A/G	0.429688	0.173817	intron-variant	Fchsd2	Mm_Celera	7:101154722	TGACCTTGGCCTCCC[A/G]CCTGGCCTTGCGCTT	207278
rs31521033	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101162443	TTTAATAATCTTCTA[C/T]CTCACTTAATGGCTT	207278
rs31525470	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101134418	GAGTCAGACCCTGCT[C/T]CCACTGTTAGGAGTC	207278
rs31529727	snp	G/T	0.456747	0.140554	intron-variant	Fchsd2	Mm_Celera	7:101154765	CCTGAACACATCCTT[G/T]TTGACAACAGTCTTG	207278
rs31542056	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101166250	CACTTTCCTGTCCTG[A/G]CATTCCCCTACACTG	207278
rs31549806	snp	C/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101129096	ATGCTTTTGCTCCTA[C/G]AGGCGGCAGAGGCAG	207278
rs31551765	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101123819	TGATTGCTGCTGGGC[A/T]GGATGGGTGACAGGG	207278
rs31556455	snp	G/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101214152	GCATATGGGGTTTTT[G/T]TGTGTGTGTGTGTGT	207278
rs31556487	snp	A/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101109734	ATCCAGAACCTGGCG[A/T]TGCATGGTTTGAGCA	207278
rs31556884	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101116193	TGAGTTTGAGGCCAC[C/T]GTAGGTTCATAGCAA	207278
rs31558198	snp	C/T	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101190625	TTGCTATTCATTTTA[C/T]TTACCCATATCTTTC	207278
rs31559146	snp	A/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101216312	CACACACACACACAC[A/T]CACACACAGAGAGAG	207278
rs31559595	snp	A/T	0.359862	0.224567	intron-variant	Fchsd2	GRCm38.p3	7:101161552	TTAATAACTCTTTTT[A/T]AAAACTCCTTACCAA	207278
rs31566596	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101208729	TGTTTAACTATTTGA[A/G]AAACAACCATACAAG	207278
rs31567691	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101223230	CAGTTTCTGGCTTTT[A/T]CAAATAAAGCTGCTA	207278
rs31568216	snp	C/T	0.375	0.216506	upstream-variant-2KB	Fchsd2	Mm_Celera	7:101107682	ATGTGACCTTGAGAA[C/T]GGCTCCAATTCTCTG	207278
rs31568492	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101261488	CATGCCCCAATTCCT[A/G]ATCATGTTTCCCTTT	207278
rs31573429	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101109859	AAGGCTGTGTCCTTG[C/T]CTTTTTAAATCTTTC	207278
rs31573704	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101207752	TAGTGAAGTACATAT[A/G]TAAACAGAAATGTGG	207278
rs31574967	snp	A/G	0.46875	0.121031	downstream-variant-500B	Fchsd2	GRCm38.p3	7:101284776	CCAGCACTTACCTGG[A/G]GCAGGGTTAAAACCT	207278
rs31576442	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101132124	TGTAACCTAGACAGA[C/T]CTGGAAATCTCTATG	207278
rs31589682	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101123535	TGGTAGAAGAAGGAA[A/C]GACAGTTTCTTCCTA	207278
rs31591417	snp	A/G	0.304688	0.243945	intron-variant	Fchsd2	GRCm38.p3	7:101247421	GAGGAGCTCACTGAC[A/G]TGGTCACAGATAAGA	207278
rs31595262	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101282336	GCTGTTCAGGGCAGT[A/G]AACACATTCCCAGGC	207278
rs31598593	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101193557	TCTCTGAGTTCATGC[A/G]TGCAGCTGCCCCACC	207278
rs31601694	snp	A/G	0.432133	0.171253	intron-variant	Fchsd2	Mm_Celera	7:101252100	CAATACTGCAATACA[A/G]TGAACAAGCAACATG	207278
rs31602487	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101254397	ATCCGTAACAAGATC[A/T]GACTCCCTCTTCTGG	207278
rs31606902	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101125385	TCAGAGCTGGCTGAC[A/G]TGGCTTGTCCTGCTC	207278
rs31617828	snp	C/T	0.345679	0.230967	intron-variant	Fchsd2	GRCm38.p3	7:101196355	TCAAGACAAACCTTG[C/T]AGCTTCAGAAAAATC	207278
rs31619856	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101197369	CCTTCAGCCAAGCTT[A/G]ATGACCTGAGTTCAA	207278
rs31624000	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101224637	AATTTTAAATTGTTG[G/T]TATGAGGTCTCTCTA	207278
rs31628348	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101167454	CACTTAGTCAAACTT[A/C]CTGCGCTGGCTTGCC	207278
rs31630406	snp	A/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101224904	CACTATTTCAATTTT[A/T]TTTTTTATCTGTTGA	207278
rs31636319	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101147941	CAGGACTTCTGCTTG[C/T]TCTGTCCTAAAGAAT	207278
rs31639822	snp	C/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101215587	AGACACACCTATTTT[C/T]CTGAGATCTAGTCTA	207278
rs31640704	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101147141	ACAACTTATTGTACA[G/T]TAGCTTCAGTAATAG	207278
rs31640845	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101266497	TTTAGATTTCTAATT[C/T]ACTTATGTTGTAGAT	207278
rs31641627	snp	A/G	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101119338	AGCTTTCATGATTCT[A/G]AAAGAAGCTAAAGGG	207278
rs31648240	snp	C/T	0.49827	0.0293608	intron-variant	Fchsd2	GRCm38.p3	7:101139105	TAAATTTACATGGGG[C/T]TTTAAAGTTCTGCTC	207278
rs31654445	snp	A/G	0.415225	0.187619	intron-variant	Fchsd2	GRCm38.p3	7:101276137	AGTGCTTCCAGAAGA[A/G]TCCTGGGCATTGCTC	207278
rs31654934	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101279643	TGTGTAGATTTGTTT[C/T]AGGGGTCTCTGATTG	207278
rs31666573	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101266652	TTGGCTGATGGCACT[G/T]CCTATGTCTTCCATA	207278
rs31668276	snp	G/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101110031	TACTGATCCTCCCCC[G/T]TTCCCCCTGCACGTG	207278
rs31670526	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101107803	AGTACTCTGGAATAG[A/G]GCATCCATTCCTTTG	207278
rs31671297	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101181591	TACCATGTGCTTGGA[A/G]ATTATATTTCTAGGC	207278
rs31672105	snp	C/T	0.493827	0.0552116	intron-variant	Fchsd2	GRCm38.p3	7:101170317	ATTTGAGATAGCATG[C/T]GTGATTTTATCTGAA	207278
rs31678100	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101209418	AATATGGCGGAGAGC[A/G]ATAGAAGAAGATGCC	207278
rs31684865	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101260862	TAGTTGGTGGCTCAG[G/T]GTCAAAGATCTAGGG	207278
rs31685601	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101230419	ATCCAGAGTTCACAG[C/T]GATCAAGAGAAGCCC	207278
rs31700131	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101113020	TGGCAATTTTCCCCA[A/G]AGTGTTCCAGCATAA	207278
rs31704911	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101136542	GCTGGGATTAAAGGT[A/G]TGTGCCACCACGCCC	207278
rs31705925	snp	A/G	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101215568	GAGAATGAGATCATG[A/G]AGTAGACACACCTAT	207278
rs31709943	snp	A/G	0.231111	0.249285	intron-variant	Fchsd2	GRCm38.p3	7:101255651	TTATCTTAGTTTTAA[A/G]TATCTGTAAAATTGT	207278
rs31711024	snp	A/G	0.465374	0.126941	intron-variant	Fchsd2	Mm_Celera	7:101154685	CATTTGTTCTTCCCT[A/G]TCTTGTATCGCTCCT	207278
rs31714009	snp	A/G	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101184958	TTCCTTTTTAAATCT[A/G]ATACATACTATTCTG	207278
rs31720512	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101146749	TCATAGCTGTCTTCA[G/T]ACATTCCAGAAGAGG	207278
rs31721345	snp	C/T	0.415225	0.187619	intron-variant	Fchsd2	Mm_Celera	7:101215510	CATCATTGGCCTGAC[C/T]AACATTAAGGACTCA	207278
rs31721785	snp	C/T	0.465374	0.126941	intron-variant	Fchsd2	GRCm38.p3	7:101249903	TGTCTCCACCCTGGG[C/T]CGGAGATATTCCATT	207278
rs31728451	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101141942	CTTTGGAAGAGCAGT[C/T]GGGTGCTCTTACCCA	207278
rs31737853	snp	A/G	0.415225	0.187619	intron-variant	Fchsd2	GRCm38.p3	7:101230421	CCAGAGTTCACAGCG[A/G]TCAAGAGAAGCCCTT	207278
rs31741969	snp	C/G	0.456747	0.140554	intron-variant	Fchsd2	GRCm38.p3	7:101275851	TTCTTACTAGAGAAC[C/G]GGAAGGCAAATGTCA	207278
rs31746299	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101218425	TTTAGTCCCTGGAAG[C/T]TCTGGGGGTACTGGT	207278
rs31747626	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101207111	ATTGGTGATCTTGCA[C/T]ATATTTTGTTAAGTT	207278
rs31747758	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101227645	ACACTGGAGATGGCC[A/G]CAGTAGTTGGGCAAA	207278
rs31761137	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101264084	CCTCAAACTCACAGA[A/G]ATCCTTCTGCTGCTG	207278
rs31768660	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101213738	GCACCAGGCATATGA[A/G]TGGTGCATAGACATA	207278
rs31770147	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101201840	GTGACAGGGAGGTAG[A/G]AAATAGGGAGTACCC	207278
rs31772984	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101127943	CACGCTGACTCATGA[A/G]GACACTCAAGATTAA	207278
rs31776805	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101119548	GTGTTGGGAGTGAAT[C/T]AAGAGAAGGAACGAG	207278
rs31776808	snp	G/T	0.35503	0.226867	intron-variant	Fchsd2	Mm_Celera	7:101120859	TCTCAAGCTTTAATG[G/T]AAGAAACTCATCATG	207278
rs31776811	snp	C/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101120990	GATTGAACATGCTAG[C/T]CAAGTGTACTACTAT	207278
rs31777154	snp	C/T	0.336735	0.234472	intron-variant	Fchsd2	GRCm38.p3	7:101163332	TGGAAGCTATGTATG[C/T]TGGGCTAGTCAGAGA	207278
rs31777156	snp	A/C	0.152778	0.230321	intron-variant	Fchsd2	GRCm38.p3	7:101163353	TAGTCAGAGAAATTA[A/C]ATCAAATACATCACA	207278
rs31777158	snp	A/T	0.484429	0.0868505	intron-variant	Fchsd2	GRCm38.p3	7:101163557	TAAAAAGCATTTTTT[A/T]AAATTTAGCAGTTTT	207278
rs31777162	snp	G/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101164866	TGTATGCTCGGAATT[G/T]TTCTGATGTTTAGAT	207278
rs31777195	snp	C/G	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101142605	TGCCTTCAAGCACAT[C/G]CAATACTTGTAATAC	207278
rs31777198	snp	C/T	0.46281	0.131194	intron-variant	Fchsd2	GRCm38.p3	7:101143814	CTAGACTTTCATCTT[C/T]CTATGGCTGTTCTGT	207278
rs31777200	snp	A/G	0.297521	0.245442	intron-variant	Fchsd2	GRCm38.p3	7:101146310	AGGATATCATCTGCT[A/G]CTCTGGATTTGAGGA	207278
rs31777202	snp	C/T	0.345679	0.230967	intron-variant	Fchsd2	GRCm38.p3	7:101149032	TAAGAACTAATCAAA[C/T]CTTAAGTATCCATCT	207278
rs31777584	snp	C/T	0.142012	0.225474	intron-variant	Fchsd2	GRCm38.p3	7:101121073	GAATGACTGAAGTAA[C/T]TCAAAGAATAAGCTC	207278
rs31777587	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101121173	CTTTCTGTATGTAAG[A/G]AAAGATCAGTGTCTA	207278
rs31777592	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101122636	TTTTAGATAGGGTCA[C/T]TGTAGCTTAATAATT	207278
rs31778145	snp	A/C	0.152778	0.230321	intron-variant	Fchsd2	Mm_Celera	7:101149686	CAAAAAAGACGGTAC[A/C]GTAACACTTCCTAAG	207278
rs31778147	snp	A/C	0.42	0.183303	intron-variant	Fchsd2	GRCm38.p3	7:101149802	AATATTTAGTGTAGT[A/C]CTTGATGCCTTATAA	207278
rs31778149	snp	A/G	0.336735	0.234472	intron-variant	Fchsd2	Mm_Celera	7:101151420	TATGCCTATACACTC[A/G]GTGTTAATTGCTGTG	207278
rs31778151	snp	C/T	0.459184	0.136902	intron-variant	Fchsd2	Mm_Celera	7:101152824	ACCCTTCATTCGAAT[C/T]CTAACATTTAGTATA	207278
rs31778153	snp	A/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101152916	TTTTGGTCAATGTTA[A/T]ACTACATTTTGGAGA	207278
rs31778205	snp	A/T	0.297521	0.245442	intron-variant	Fchsd2	Mm_Celera	7:101165707	TTCAAAATTATTATC[A/T]AGTACTGTATCTATA	207278
rs31778208	snp	A/C	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101166043	ATGCTTTGTCTCAGC[A/C]TTTGCATCCCCTCTT	207278
rs31778210	snp	A/T	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101168611	CACAGATGCACACAT[A/T]CTCCCATACCAAGCA	207278
rs31778212	snp	C/T	0.497778	0.0332592	intron-variant	Fchsd2	GRCm38.p3	7:101168675	GTGATGGAGCAACTT[C/T]AACTTAAAGAAAAAT	207278
rs31778495	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101122844	AAGCACTGTGTAGAT[A/G]CTTACCATTGTACTA	207278
rs31778500	snp	G/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101124017	TAGGAGGGTACATAG[G/T]GACCAGTAAGCCAGT	207278
rs31778503	snp	A/T	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101124112	TTGATGGTTTACGGA[A/T]GTGTCAATCTAAGAG	207278
rs31779336	snp	C/T	0.336735	0.234472	intron-variant	Fchsd2	Mm_Celera	7:101153217	GATTTGTGTTTTTCT[C/T]GGGTTTATTTTACTT	207278
rs31779339	snp	C/T	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101154105	CGATTTAAAAACAAA[C/T]TGCAGCTTATGCTTG	207278
rs31779342	snp	G/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101154280	TGCATTTATGATTCA[G/T]AAAGGAGTATAATGA	207278
rs31779375	snp	A/G	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101168874	TTCTCTACTCTTTGA[A/G]CTTTGAGATGTTATG	207278
rs31779379	snp	C/T	0.33241	0.236027	intron-variant	Fchsd2	GRCm38.p3	7:101170786	TTTTAAGTTTGAAAA[C/T]AGGAGAAACCAAATC	207278
rs31779382	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101170849	CTTTCACTCTAGCTA[C/T]TTTTCACCCTGAAAA	207278
rs31779386	snp	C/G	0.497778	0.0332592	intron-variant	Fchsd2	Mm_Celera	7:101126281	TGGCTATATAGATGT[C/G]AGCTCAAAGTTATTT	207278
rs31779389	snp	C/G	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101126360	TCCTGCTTGTGTTTG[C/G]GAACTAAAGTGACAC	207278
rs31779391	snp	C/T	0.336735	0.234472	intron-variant	Fchsd2	Mm_Celera	7:101126463	ATGTAACAAGGGGAG[C/T]AGGGCTAGATGCAGC	207278
rs31779393	snp	G/T	0.426035	0.177515	intron-variant	Fchsd2	GRCm38.p3	7:101127005	TGTGTTTTTAAAAAA[G/T]TTATAAGAACTGGTA	207278
rs31780125	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101154415	AATCCAAAGTATATT[C/T]GCACAATAGTATTTT	207278
rs31780215	snp	A/T	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101171965	ATGTTGCTTTTACTC[A/T]GAATCGAATAAAAGA	207278
rs31780218	snp	C/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101172763	AGGTTTGAAATAATT[C/G]TTTGTTTGTGTTTTA	207278
rs31780221	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101173508	TGCTCAGCTTGGTGT[C/T]GTGAATGGGCCAAAG	207278
rs31780268	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101113932	TAGATGTTTTAGAAG[A/G]CATTTCTAGATGAAA	207278
rs31780271	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101114010	AAGTAGAGATCTTGC[C/T]TGGGGCATGTGGTCA	207278
rs31780395	snp	A/T	0.35503	0.226867	intron-variant	Fchsd2	GRCm38.p3	7:101127583	TAATTCATCCCTCAA[A/T]ATCAGAATTCAGGAA	207278
rs31780398	snp	A/C	0.359862	0.224567	intron-variant	Fchsd2	GRCm38.p3	7:101127666	TTAGAAACAGTAAGG[A/C]TCTGAGCATGGAGGG	207278
rs31780401	snp	C/T	0.359862	0.224567	intron-variant	Fchsd2	GRCm38.p3	7:101127696	GGCGTGACTGTAATT[C/T]TAGTGTTCCAAGGCA	207278
rs31781114	snp	A/G	0.486111	0.0821678	intron-variant	Fchsd2	GRCm38.p3	7:101173758	GGAATTATATTGCTA[A/G]TCAAAGGAACTTTTT	207278
rs31781117	snp	A/G	0.456747	0.140554	intron-variant	Fchsd2	GRCm38.p3	7:101173814	ATAAATATATCCCTA[A/G]TGGACCAGTTTTGAG	207278
rs31781120	snp	C/T	0.345679	0.230967	intron-variant	Fchsd2	GRCm38.p3	7:101174021	CAAGTATAAAAAATG[C/T]TCTCAGAGGCATGAA	207278
rs31781123	snp	C/T	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101174050	AACTGTTATTTAGGA[C/T]CTTACTGATAATGGT	207278
rs31781124	snp	C/T	0.277778	0.248452	intron-variant	Fchsd2	Mm_Celera	7:101155006	TTGCGTCCGGAGTAG[C/T]GTCCGGCCAGGATCA	207278
rs31781127	snp	C/T	0.459184	0.136902	intron-variant	Fchsd2	Mm_Celera	7:101155019	AGCGTCCGGCCAGGA[C/T]CAGCACCACTTTACC	207278
rs31781130	snp	C/T	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101155348	TGAATAAAGATGGTG[C/T]GGTGGTTCATACGTG	207278
rs31781133	snp	A/C	0.492188	0.0620098	intron-variant	Fchsd2	GRCm38.p3	7:101155481	ACAAGAATGAAAGGT[A/C]ATTTGGAAGGGTTAT	207278
rs31781204	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101114307	TATAGATGCAACATA[C/T]ATTAAGCTAGGTTGA	207278
rs31781207	snp	C/T	0.33241	0.236027	intron-variant	Fchsd2	GRCm38.p3	7:101114425	TTATCACAGCAGTCT[C/T]TTCATGATTTCCTTT	207278
rs31781210	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101114536	CCACAGACCTCTTTT[C/T]CTAGCTTAATTATTA	207278
rs31781466	snp	A/G	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101129035	AAAAAGGAAGGTTAC[A/G]TGAGTGCTTTTAAAA	207278
rs31781471	snp	A/C	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101129534	TACTTATATGTGCAC[A/C]GCAGTAAAAATGAGT	207278
rs31782006	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101155825	CTCTTTCTCTCACTA[A/T]TTTGTGAATGGATAA	207278
rs31782009	snp	A/G	0.459184	0.136902	intron-variant	Fchsd2	GRCm38.p3	7:101156534	CTGGAAATAAAATAC[A/G]TAAAAAGTTTTAAAG	207278
rs31782012	snp	C/T	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101156988	ACTTGCTCCAAAGAT[C/T]CACGAAAGTACTAAA	207278
rs31782066	snp	A/G	0.345679	0.230967	intron-variant	Fchsd2	GRCm38.p3	7:101174140	AGAATCACGATTCCC[A/G]TCTCTGTGAACTAAC	207278
rs31782069	snp	A/G	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101174621	GGTCTCTTTCACAGA[A/G]TTAAGAGAAAATGTG	207278
rs31782072	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101175659	GAAAACTTATTGTGG[A/G]TCTTGGTTAGAAACT	207278
rs31782137	snp	A/C	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101117541	ACCCTAGAAGACACT[A/C]AGATAAATGAGACAA	207278
rs31782324	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101131256	GTGAGTTTTATTTCA[A/G]TGGGCTTGCATGCAT	207278
rs31782327	snp	C/G	0.277778	0.248452	intron-variant	Fchsd2	GRCm38.p3	7:101131532	TGCTTCTTCAGAACA[C/G]GAAGGAAACCCCTCT	207278
rs31782332	snp	C/G/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101133159	AGCCACTGCATTATC[C/G/T]AAAGCCTTGTCCAGA	207278
rs31782506	snp	G/T	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101181003	CTAAATAAGTAAATA[G/T]TGTCTGTAGGTTGAC	207278
rs31782509	snp	A/G	0.152778	0.230321	intron-variant	Fchsd2	GRCm38.p3	7:101181272	CTTCCTTGCCAACAA[A/G]AGGAATTTAAATTTT	207278
rs31782515	snp	A/T	0.124444	0.216185	synonymous-codon	Fchsd2	Mm_Celera	7:101198558	GACGCTAGCAGCAGC[A/T]AACGCACATCAGGAC	207278
rs31782520	snp	A/G	0.35503	0.226867	intron-variant	Fchsd2	GRCm38.p3	7:101200251	ACTATGTGACTGCAG[A/G]TGATCAGAATGCAAG	207278
rs31782523	snp	A/G	0.244898	0.249948	intron-variant	Fchsd2	GRCm38.p3	7:101200823	TTCAAATGAAGACGG[A/G]ATTCTTTTTTTGTTG	207278
rs31782574	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101219641	GTTAAAGTTCTTTAT[A/C]GGAAACCCAGTTTGC	207278
rs31782576	snp	A/G	0.260355	0.249785	intron-variant	Fchsd2	GRCm38.p3	7:101221348	CCTCTGCTTGTCTAT[A/G]TCTTTGAAACTTAAT	207278
rs31782579	snp	C/T	0.207612	0.24638	intron-variant	Fchsd2	Mm_Celera	7:101222424	ACAAATAATTCAAAG[C/T]GGGAAGAAAGATAAA	207278
rs31782677	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101260486	TTTGACAGGTAATAA[A/G]CAGCACACAGCTTGT	207278
rs31782680	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101260675	AGATACTTGTGTTTG[C/T]TGCAGGAAGAACTGA	207278
rs31782683	snp	A/C	0.142012	0.225474	intron-variant	Fchsd2	Mm_Celera	7:101260698	AGAACTGAGTGGATG[A/C]ATGGAAGGATGTACC	207278
rs31782686	snp	A/G	0.231111	0.249285	intron-variant	Fchsd2	GRCm38.p3	7:101239356	TGTGTTTTTAAATTG[A/G]TGTAAAACCAAACAT	207278
rs31782689	snp	C/T	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101242992	TAAATACTGTTCACG[C/T]CTAGCCTTTCTCAAG	207278
rs31782692	snp	A/G	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101243028	TCACGCAGTAAGTTG[A/G]CTTTCAGACTCAAGA	207278
rs31782734	snp	A/T	0.142012	0.225474	intron-variant	Fchsd2	Mm_Celera	7:101157031	TACACAAAATAGATG[A/T]CAGAATAGAGGGGGA	207278
rs31782736	snp	C/T	0.408163	0.193609	intron-variant	Fchsd2	Mm_Celera	7:101158710	CTTAAAGATACCAAT[C/T]TGTTCCATGAATAGT	207278
rs31782739	snp	G/T	0.489796	0.070696	intron-variant	Fchsd2	GRCm38.p3	7:101159595	AGCAAGGTATTAAAA[G/T]GTTTCTAGATAGTCC	207278
rs31782741	snp	A/G	0.459184	0.136902	intron-variant	Fchsd2	GRCm38.p3	7:101161056	TATTAAGTTTCTGTT[A/G]TTCATCAGCATTTAG	207278
rs31782743	snp	A/C	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101161131	GTGATCCTGTGTATG[A/C]AGTATAAATGCATGT	207278
rs31782825	snp	C/T	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101176939	AGTTCAAGAAACCAG[C/T]GTTTATCAGTTCCAC	207278
rs31782828	snp	A/C	0.336735	0.234472	intron-variant	Fchsd2	GRCm38.p3	7:101176944	AAGAAACCAGTGTTT[A/C]TCAGTTCCACAGTGA	207278
rs31782831	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101177262	TGCATGTATGTGTGC[C/T]CATGTGTGTATGTGT	207278
rs31783066	snp	C/G/T	0.124444	0.216185	intron-variant	Fchsd2	GRCm38.p3	7:101119530	GTGGATTTGGAAACT[C/G/T]GAGTGTTGGGAGTGA	207278
rs31783107	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101133859	GTCTCTATCCAAATG[C/T]GCATGTATGTGGATG	207278
rs31783113	snp	A/T	0.46875	0.121031	intron-variant	Fchsd2	GRCm38.p3	7:101138339	GTCTATTTGTGTCGG[A/T]CAGTCTGTCTGTCTG	207278
rs31783426	snp	A/C/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101201525	CTAAATTGTGGAAGA[A/C/T]GCAAAAGCAAATGGG	207278
rs31783429	snp	A/C	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101203357	CAAACATCCCATGTT[A/C]ATTACTCTGTAGGAT	207278
rs31783432	snp	A/C	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101203563	TTAAACTAAAAAAAA[A/C]CCCTATTGATAGACT	207278
rs31783485	snp	C/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101243323	ACATAAGTAAGAATT[C/G]AATTAAACAAAAAGT	207278
rs31783488	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101246606	CCTTAACTTTCCTCA[A/G]CAGGGAGACATTGAG	207278
rs31783491	snp	C/T	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101246729	TGATGGCAATATTTA[C/T]ATTCTTTCTGATATA	207278
rs31783566	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101261923	AACCAGTCTTACAGA[A/G]CCTGTGTATTCCCTC	207278
rs31783569	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101262280	CTGTCTTAGAGAACC[A/G]TATTTACATGATAAT	207278
rs31783571	snp	A/G	0.473373	0.11227	intron-variant	Fchsd2	GRCm38.p3	7:101262645	GGGTTACTGCCAGTG[A/G]TCCTGTGAGCCACTA	207278
rs31783584	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101177823	CCATATATGGAATGG[A/G]AAGAACAGAAACACA	207278
rs31783587	snp	A/G	0.336735	0.234472	intron-variant	Fchsd2	GRCm38.p3	7:101177917	ACTGCTGTCATGCTC[A/G]TTGATTTGTCCAAAG	207278
rs31783590	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101177962	TTAAGTTGAGATTAT[C/T]GTGAGCTTGAGTATT	207278
rs31783593	snp	A/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101178003	CTAGAAATGTTTGTG[A/T]ATAACAGGCTGTCCA	207278
rs31783596	snp	A/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101184992	GCAACACAGTTGTCC[A/T]CAAGCACATCACTCC	207278
rs31783599	snp	C/T	0.473373	0.11227	intron-variant	Fchsd2	GRCm38.p3	7:101185985	CACAGCAGAGACAGA[C/T]GCAGAGCACTGCCAC	207278
rs31783602	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101187521	CAGGAGGCCAAAGCA[A/G]GGACATTGCAAATTT	207278
rs31783805	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101161427	GTGACAAACTCTTAT[A/G]TTGTGCTTCTTTTAC	207278
rs31783808	snp	C/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101162634	TGAGAGTAAATTCTA[C/T]AACCTTAGCCAGTAG	207278
rs31783810	snp	A/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101162659	CAGTAGTCTCTAATA[A/T]AGGGTGCCCACACTT	207278
rs31783812	snp	C/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101163058	TGAATGGTTATCCTG[C/T]GTACCTCATAGGCAG	207278
rs31783974	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101225328	GCAAGAATGCACAAG[A/G]AAAAAGGAGTCAATA	207278
rs31784060	snp	G/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101141755	ACTAACATGGCATTT[G/T]GGTCAGATGTCCATT	207278
rs31784195	snp	A/G	0.345679	0.230967	intron-variant	Fchsd2	GRCm38.p3	7:101203630	AAAGCAGCTCAGTTG[A/G]CTGAGAGGTGAGGCA	207278
rs31784198	snp	C/T	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101204303	CTCCCTTTTCTTGCT[C/T]ACCATCAACCCAGAA	207278
rs31784200	snp	C/T	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101204320	CCATCAACCCAGAAG[C/T]CTTTCTCACTTATTT	207278
rs31784203	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101204347	ATTTTAGTTATAGTC[C/T]TGATGTCTGTGCTTA	207278
rs31784326	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101178166	ATTTGGAATGACTTA[C/T]TGGCTTTTGTATTCA	207278
rs31784329	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101178636	GTGTGGAGAATACAT[A/G]AGTAAGCATCATAAA	207278
rs31784332	snp	C/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101179144	CAGACAAAGCCAATG[C/T]TGCTTCTTTAAACAA	207278
rs31784374	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101247148	AGAGCTACTATTTAA[C/T]GTCTTCCTTTTAGAG	207278
rs31784377	snp	A/G	0.207612	0.24638	intron-variant	Fchsd2	GRCm38.p3	7:101247161	AATGTCTTCCTTTTA[A/G]AGTTGGTAGCCCTAA	207278
rs31784435	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101187617	TCAGAAAAAAAGATT[A/G]ATTATATATGCATAA	207278
rs31784440	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101188420	CAATTTTAGAGAAAA[C/T]GTGCACATAGCATAT	207278
rs31784564	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101262718	GCTTAAATCCATTCC[C/T]GGTTTATAACCTAAT	207278
rs31784567	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101262804	TCTAATTTTTCTTGT[C/T]CCTGGATAATCTTCA	207278
rs31784570	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101262876	TTTACATAGATGCAA[C/T]TGATCATTCATATTT	207278
rs31784573	snp	G/T	0.495868	0.0452663	intron-variant	Fchsd2	GRCm38.p3	7:101262969	ATAGAAATTTTTCTA[G/T]TAAGCATGTTGTCTT	207278
rs31784684	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101276085	AGCTGCAATCATTGG[C/T]TTGCTCATAACTTTC	207278
rs31784689	snp	C/T	0.277778	0.248452	intron-variant	Fchsd2	Mm_Celera	7:101276225	AAGTGTCTTCTCTGT[C/T]ACTCACACCTCAGGT	207278
rs31784905	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101180382	TCTGTGCAATTTATT[C/T]ATGATTTATTCATTT	207278
rs31785075	snp	A/G	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101204672	ACAGGTATTGTTAAT[A/G]TAGATTGTAAGGCTC	207278
rs31785078	snp	C/T	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101204924	TCTGTCTTTGTTGCT[C/T]TGGTTTGATTCTCTT	207278
rs31785080	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101205496	CACATGGTTTAATGG[C/T]TTCAAAAATGAAATA	207278
rs31785082	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101205531	TAGTACAATGGAATC[A/C]TATGTGATGCCTCCA	207278
rs31785084	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101169044	ACATCTTTTTGTAAG[C/T]AATTATTTATGTTGT	207278
rs31785105	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101228675	TGGGTTTTTAAATGC[C/T]GTTGGACTATTCCTA	207278
rs31785108	snp	A/G	0.42	0.183303	intron-variant	Fchsd2	GRCm38.p3	7:101229646	TCCCTCCTCCCAGAT[A/G]TTTACAGCCTCAGCC	207278
rs31785111	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101229657	AGATATTTACAGCCT[C/T]AGCCTGACTGCTGTT	207278
rs31785238	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101264174	TTCTGTGGAATACAA[A/G]CATTAGTTTCTTCTT	207278
rs31785241	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101264421	TCTCAAAAATAAGTA[A/G]AATAGTGATAATGCT	207278
rs31785294	snp	A/G	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101247477	CATTTTCTTCTTCAT[A/G]GCCAGTAACTGATAT	207278
rs31785297	snp	A/G	0.465374	0.126941	intron-variant	Fchsd2	GRCm38.p3	7:101249594	GTGCTGGAGCTGACC[A/G]AGTTTGAAAGTGAGT	207278
rs31785302	snp	A/G	0.391111	0.206368	intron-variant	Fchsd2	Mm_Celera	7:101251833	TAGTGAAGGGTAGGT[A/G]CAACCTATTGGAGAT	207278
rs31785447	snp	C/T	0.391111	0.206368	intron-variant	Fchsd2	Mm_Celera	7:101190828	CCACCATATCCAATA[C/T]ATTCTCAACTGATTT	207278
rs31785450	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101191371	TTGCTTTTATTGTCA[A/G]GATATTTGCAGTAGC	207278
rs31785716	snp	G/T	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101277114	TTCCTATAATTGATA[G/T]CACTAGTCTTGATCA	207278
rs31785719	snp	A/C	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101277147	AGAAGCATAAAGATA[A/C]TCTCAGTGAATAATG	207278
rs31785722	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101277704	AGTGTTTACATAACT[A/G]AGTTTAGAAATTAGA	207278
rs31785906	snp	A/T	0.336735	0.234472	intron-variant	Fchsd2	Mm_Celera	7:101231226	TATTATCATGTCTTG[A/T]ATATAGGTAAAATGA	207278
rs31785909	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101231695	TCTGCTTCGGGGACA[A/G]GTTTTGTTTTATTTC	207278
rs31785912	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101232973	TGAAACTCTAAAACA[A/G]AAACATTTTATTTGG	207278
rs31786134	snp	G/T	0.197531	0.244432	intron-variant	Fchsd2	Mm_Celera	7:101264714	GAGGTGTCTGCCTCT[G/T]CAGCCCTCAGACCAC	207278
rs31786137	snp	G/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101264800	ACTGTGTAGTTTGGG[G/T]TTTTTTTCCCAATCA	207278
rs31786140	snp	C/T	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101264967	TGTTTGACATGTGTA[C/T]ACCAGTGAAAGCATT	207278
rs31786142	snp	A/G	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101265537	TTGAATTTGTATAGG[A/G]CATGTACTACTAACA	207278
rs31786165	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101206533	AGTTCTTTTTCAGAT[A/C]AGTTTTTAAGTGTAC	207278
rs31786167	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101206560	GTACAGGTAACATAC[A/C]AAAAATGAATCTATT	207278
rs31786169	snp	A/C	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101207872	TTATTTGTTTAGTAA[A/C]TCATGTGTGGGCTAC	207278
rs31786172	snp	G/T	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101209026	GTATGGTGAGTTAGA[G/T]GTCAGCTGATGGACG	207278
rs31786195	snp	A/G	0.277778	0.248452	intron-variant	Fchsd2	Mm_Celera	7:101252004	ATTTGGCAGTATCTA[A/G]TAATACTAAAGTATA	207278
rs31786197	snp	G/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101252074	TTGTGCAGGGCAGTT[G/T]GCTTGATCACCAATA	207278
rs31786201	snp	C/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101253170	CAACTCAACTTTCAC[C/T]TAATTGTGGCCTTAC	207278
rs31786203	snp	A/G	0.124444	0.216185	synonymous-codon	Fchsd2	Mm_Celera	7:101253541	ACAGGTTCTAAATGA[A/G]CTAGAATGTCATGGA	207278
rs31786445	snp	A/T	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101191941	TGTCTTCTGTGCTGT[A/T]GACCACACTTTTTCT	207278
rs31786448	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101192735	CTCGGCCTTCAGATA[C/T]CTAGGATAAAGCAGT	207278
rs31786451	snp	C/T	0.35503	0.226867	intron-variant	Fchsd2	GRCm38.p3	7:101193861	ACTATTATTATCACT[C/T]TGTGTGTAGGTATGG	207278
rs31786453	snp	A/C	0.42	0.183303	intron-variant	Fchsd2	GRCm38.p3	7:101194022	TTTAAATTGAGAAAA[A/C]CTACTCAGTCTAGTA	207278
rs31786565	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101278688	AGGGTTATAGATTGC[A/G]TAGTTCTTCCAAATT	207278
rs31786568	snp	G/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101278810	AAAGGCTATATTTTT[G/T]ATTGTACTCCCAGCC	207278
rs31786571	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101280976	TCATTCAGCTGATAT[A/G]CATTGAGAACCTTGT	207278
rs31786755	snp	G/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101233572	AATTGTCATGAAGTG[G/T]CTACAGAAGCAGATA	207278
rs31786758	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101233749	CTTATGTAATGCTCT[A/G]TGCCTTTTGTCAGTT	207278
rs31786761	snp	A/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101233830	ATTATGTGCCAAAGC[A/T]CTATCATAATTTTTG	207278
rs31787064	snp	C/T	0.277778	0.248452	intron-variant	Fchsd2	GRCm38.p3	7:101265555	TGTACTACTAACATA[C/T]GCTTTTGAATATGCT	207278
rs31787066	snp	C/T	0.459184	0.136902	intron-variant	Fchsd2	GRCm38.p3	7:101265597	ATATAGTTAATGTTT[C/T]AAGAAACTAATCCTG	207278
rs31787069	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101265883	CGGATAATCAACACC[A/G]AGGCTGTTCTCCTTT	207278
rs31787072	snp	A/G	0.426035	0.177515	intron-variant	Fchsd2	GRCm38.p3	7:101267128	AGAGGTCAAAGGACA[A/G]CTTGCAGGAGGTGGC	207278
rs31787205	snp	G/T	0.401235	0.199068	intron-variant	Fchsd2	GRCm38.p3	7:101211407	CGTACTCTGTGCTGA[G/T]CTTCCATATCTACCA	207278
rs31787208	snp	A/G	0.277778	0.248452	intron-variant	Fchsd2	GRCm38.p3	7:101212823	ACACAAGCTATTAAT[A/G]GAATTGAGAAGTATG	207278
rs31787211	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101213165	TGACCATAGGAAGAA[A/G]TCATGCCAGGTGTAT	207278
rs31787297	snp	C/T	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101194730	GATGATCGATGATTT[C/T]GTAGATGGTGCTAGA	207278
rs31787300	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101194780	AAAGAGAGGATTACG[A/G]TTGAAGGAGACAGTA	207278
rs31787303	snp	A/G	0.387812	0.208586	intron-variant	Fchsd2	Mm_Celera	7:101195811	ACAGAAAAAAAAAGA[A/G]AACTGAGAATACTCT	207278
rs31787354	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101281392	AACTCACTCTTCCCG[C/T]GTGATCTCCTCCACT	207278
rs31787357	snp	A/C	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101281592	TCCCTGTCCTGGAAT[A/C]ATTTCTCCTGCCTTA	207278
rs31787360	snp	A/C	0.132653	0.220748	intron-variant	Fchsd2	Mm_Celera	7:101281832	ACCTCTGCCTAGAGA[A/C]TAAAGTTTCTTATTT	207278
rs31787504	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101253795	TGTAGCACGTAACAA[C/T]GAAAACTCTGAACCT	207278
rs31787506	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101253975	GCAGAGATTTGATTA[A/G]GAAAAGAAGGATCAA	207278
rs31787508	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101254720	AAGCAAGCATGTTCT[C/G]TCAGAATAGACATGT	207278
rs31787510	snp	A/G/T	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101254732	TCTCTCAGAATAGAC[A/G/T]TGTCATTTGTCCCTG	207278
rs31787513	snp	C/T	0.497041	0.0383476	intron-variant	Fchsd2	GRCm38.p3	7:101254835	TGAATGTGTGGGAAG[C/T]CGTTGCAGAGTGGCA	207278
rs31787526	snp	C/G	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101234565	ATTTTTAAGGGTGGT[C/G]AATCTTTGCTTTAGG	207278
rs31787529	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101234642	GAATATTTCCTGACT[A/G]TATCCATTTTAAAAT	207278
rs31787532	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101234871	GTATCCATTTTCACA[C/T]GACAGGAATGAGAAA	207278
rs31787955	snp	G/T	0.426035	0.177515	intron-variant	Fchsd2	GRCm38.p3	7:101267163	ACCTTTACCCACAGA[G/T]CCATTTTACAGGCCC	207278
rs31787958	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101267332	AGGTTCTGCTAATCA[A/G]TTTTCTGCAAGTAGC	207278
rs31787960	snp	C/G	0.387812	0.208586	intron-variant	Fchsd2	GRCm38.p3	7:101267890	GGGTCAAGAAACCAT[C/G]AGAACAATGAAGAGG	207278
rs31787962	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101268296	AAGAATGTTTGTCCA[C/T]CCTTACTCTCTAACG	207278
rs31788024	snp	C/T	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101213349	AGCCCTCCTCCAAAG[C/T]ACACTGATCATTTCA	207278
rs31788027	snp	A/C	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101214083	CCGAATAGAACTCTT[A/C]TAAACTGTACCTGTT	207278
rs31788030	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101215372	AAACTAGAGAGACTC[C/T]AAATTATGATGGTTC	207278
rs31788032	snp	A/G	0.456747	0.140554	intron-variant	Fchsd2	GRCm38.p3	7:101215397	TGGTTCCTACAAGAT[A/G]ATACTTCTCATACAG	207278
rs31788085	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101282348	AGTGAACACATTCCC[A/G]GGCCCTCAGGTGTCA	207278
rs31788088	snp	C/T	0.401235	0.199068	synonymous-codon	Fchsd2	GRCm38.p3	7:101282521	GGAGGACGTGGAGAT[C/T]ACACTGGTGTGACAG	207278
rs31788091	snp	C/T	0.124444	0.216185	utr-variant-3-prime	Fchsd2	Mm_Celera	7:101282716	ATGTCATCTCTCCTA[C/T]CATAGCACAAATCAT	207278
rs31788296	snp	A/G	0.260355	0.249785	intron-variant	Fchsd2	GRCm38.p3	7:101195898	TACTTATGAGTCAAA[A/G]TTAATAGAAATCTGA	207278
rs31788299	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101196291	TACTAAGGCATAGCT[A/G]CCAGCACATGTGTTG	207278
rs31788302	snp	G/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101196335	CAATCACCATGACAC[G/T]GCAGTCAAGACAAAC	207278
rs31788355	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101234939	AAGTGTTCTTGTCTC[C/T]GTGTGCCTGAGCTCC	207278
rs31788357	snp	C/T	0.297521	0.245442	intron-variant	Fchsd2	Mm_Celera	7:101235909	TTTTATTAATTTTGA[C/T]AGAAATACTTTTTGT	207278
rs31788359	snp	A/G	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101238333	CTTCGGAGGGGACTC[A/G]GTGGCACCTCTAGAC	207278
rs31788361	snp	C/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101238537	TGCATTTTGCAGTTT[C/G]CTCCAGAGAATAAGT	207278
rs31788363	snp	A/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101238782	TTGAGGTTCTTCAGG[A/T]CACTGATGAGCAGGT	207278
rs31788496	snp	A/T	0.336735	0.234472	intron-variant	Fchsd2	GRCm38.p3	7:101255289	GAAAACATTAATAAA[A/T]CGGGAATGAGTATTT	207278
rs31788499	snp	C/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101255390	TGCCATGGTGCCAAC[C/G]TTAACATCACCAAGC	207278
rs31788944	snp	A/G	0.459184	0.136902	intron-variant	Fchsd2	GRCm38.p3	7:101269954	ACAGCAGTCTTCGAT[A/G]TTCCCTCATGTTAGC	207278
rs31788946	snp	A/G	0.408163	0.193609	intron-variant	Fchsd2	GRCm38.p3	7:101271783	GCATCTGCTTACACT[A/G]TGCTGGCTAGCACAA	207278
rs31788950	snp	A/G	0.459184	0.136902	intron-variant	Fchsd2	GRCm38.p3	7:101274470	GTGCATTGGCTTTTT[A/G]CCTACATGTATAGCT	207278
rs31788953	snp	G/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101274769	GAGAACAGGAGAGAG[G/T]GTTCGCTCAAGGCTT	207278
rs31788954	snp	A/G	0.132653	0.220748	utr-variant-3-prime	Fchsd2	Mm_Celera	7:101283025	ATGCAACCTTATTGA[A/G]AAGAAAGTGGACTGC	207278
rs31788957	snp	A/G	0.152778	0.230321	utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101283480	CCTTCTGAAAGTACA[A/G]CTTCAGGTCCCACTG	207278
rs31788959	snp	A/G	0.345679	0.230967	utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101283513	CTGACATTTGTCCAG[A/G]GTGAAGAATCTATGG	207278
rs31788961	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101283571	AAAGGATACAGGACT[A/G]TACACCTGCCCAGGT	207278
rs31789179	snp	A/G	0.459184	0.136902	intron-variant	Fchsd2	GRCm38.p3	7:101216587	CAGCACCCAGAATGC[A/G]TCTTTGTGGAAGTAG	207278
rs31789185	snp	C/T	0.408163	0.193609	intron-variant	Fchsd2	Mm_Celera	7:101196472	AAAACAACATATTTT[C/T]ACTACTTATGCTTAC	207278
rs31789188	snp	A/G	0.297521	0.245442	intron-variant	Fchsd2	Mm_Celera	7:101196580	GGACAGAATTCAAGG[A/G]ACTTCTTAGTAACAT	207278
rs31789191	snp	A/T	0.408163	0.193609	intron-variant	Fchsd2	Mm_Celera	7:101196594	GAACTTCTTAGTAAC[A/T]TCAGAATACCTTTAC	207278
rs31789288	snp	C/T	0.46875	0.121031	intron-variant	Fchsd2	GRCm38.p3	7:101238912	CGCTGACCAGTCCAC[C/T]ACCTCTCCAGCTGCT	207278
rs31789291	snp	C/G	0.336735	0.234472	intron-variant	Fchsd2	GRCm38.p3	7:101239063	GCAAAAATGGATCCT[C/G]AGTTTATAAGAGAAA	207278
rs31789504	snp	A/G	0.391111	0.206368	intron-variant	Fchsd2	GRCm38.p3	7:101256094	TAGTACTTTGTAATT[A/G]ATGAAAAAACTTTTA	207278
rs31789507	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101256183	CTTGCCTGAAGTTGC[A/G]GCAAAGTCATATTGA	207278
rs31789510	snp	A/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101256789	TTCTAAGTATTTGAA[A/T]TTTTTTGAAATGCAG	207278
rs31789513	snp	A/G	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101258059	TGAGTACATATGTAT[A/G]GTTGTGCTTGTGTTG	207278
rs31789944	snp	G/T	0.336735	0.234472	utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101283620	ACCTTCTGCAGGTCA[G/T]GGAAGAGCCTCATGG	207278
rs31789947	snp	C/T	0.391111	0.206368	utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101283636	GGAAGAGCCTCATGG[C/T]GCCCTGGCCTCAGCC	207278
rs31789950	snp	C/T	0.35503	0.226867	utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101284126	GATTTGAGTTTCCCA[C/T]AACCTCAGAGTTATT	207278
rs31789953	snp	G/T	0.401235	0.199068	downstream-variant-500B	Fchsd2	GRCm38.p3	7:101284522	GAGTCCACCCAGACA[G/T]CACAGACCCTGATGC	207278
rs31789988	snp	A/G	0.46875	0.121031	intron-variant	Fchsd2	GRCm38.p3	7:101275999	CCAGCTGCGGCAGAA[A/G]AGCACCTACAGCTAA	207278
rs31790004	snp	C/T	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101239224	GATTATTAGAGTCCA[C/T]ACCACTCATTGTGCA	207278
rs31790014	snp	C/T	0.345679	0.230967	intron-variant	Fchsd2	GRCm38.p3	7:101196742	AGACAATAAGCATCA[C/T]TCTTGGTTTTCCAGT	207278
rs31790017	snp	C/T	0.33241	0.236027	intron-variant	Fchsd2	GRCm38.p3	7:101197106	TGGGCACAGTTTACT[C/T]TTCAAGTCTGCTTTA	207278
rs31790177	snp	A/C	0.432133	0.171253	intron-variant	Fchsd2	GRCm38.p3	7:101258824	AAAAGACAGAAAAGG[A/C]TATTCCAAAGTGTAA	207278
rs31790334	snp	A/G	0.124444	0.216185	intron-variant	Fchsd2	Mm_Celera	7:101219205	TTGGAATAAAACCTT[A/G]GGCCCTGTTCTATGA	207278
rs31790394	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101127969	ATTAAATCTTTAGTG[C/T]TGTGCCAAAACTTTG	207278
rs31790846	snp	A/G	0.244898	0.249948	downstream-variant-500B	Fchsd2	GRCm38.p3	7:101284640	GGCTGAGTCTCTCTG[A/G]CTTCCAGACAACCAC	207278
rs31790849	snp	A/T	0.345679	0.230967	downstream-variant-500B	Fchsd2	GRCm38.p3	7:101284715	CCCCGCCTGTGCAAT[A/T]AAACCTTTTACTCAC	207278
rs31792111	snp	A/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101130363	TAGCTGTTTAGCAAG[A/G]CCCAGTGATTCCCCG	207278
rs31793500	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101116692	CATTCCTTTAATCCA[A/T]GCACTTAGAGGCAGG	207278
rs31803530	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101117737	ATGGGCACTGTGCAC[C/G]TGTGGTAAACATAGA	207278
rs31811237	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101121761	ATTGGCAAGCCTCCA[A/G]GCCAGTAAGAGACCC	207278
rs31813338	snp	A/C	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101277315	ATTGCAAGTTTGAGA[A/C]CAGGCTGGGCTACAG	207278
rs31817967	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101176333	TTCTCAGAATACATC[A/G]TATCTGGAAATAGTG	207278
rs31836499	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101183959	GACTTTGGGACACTC[C/T]AGCATTGACTGATCT	207278
rs31839462	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101261247	GGATGGCAGCCCTAT[C/T]GTTCCACTTGATGCC	207278
rs31844887	snp	A/C	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101270444	GTATCAAAAGATGGC[A/C]TAGTCGACCATCACT	207278
rs31850689	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101154514	GGTTGGGGAGGGGCT[A/G]AAGAGGTCCATATGG	207278
rs31852570	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101261394	TTCTAGAGGCCTCCC[C/T]ACACACACACACCTC	207278
rs31858244	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101274743	AGGCAAGAAAGAGCA[C/T]TGTGCGCTCAGAGAA	207278
rs31859671	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101261249	ATGGCAGCCCTATTG[C/T]TCCACTTGATGCCCT	207278
rs31864122	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101248415	AGAACATGAACTTGA[C/T]TGGGAGTAGAGATGG	207278
rs31864309	snp	A/G	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101195853	TCTTACCCTAAATAA[A/G]TACTTTCTTATCTTA	207278
rs31866787	snp	A/T	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101137749	GGCATATAATTTTTT[A/T]AAAAAGGTTTTGTAG	207278
rs31872234	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101170956	AGCTAAAATTTTAGA[C/T]GTACTTTTTAAAAAG	207278
rs31875626	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101134203	CTGACCACACTTTTC[C/T]ATCTCTTCTCTCCTC	207278
rs31900780	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101220236	GACCTTCCAATTAAC[C/T]TGCCTCCATCTCCCA	207278
rs31906255	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101190659	TTATAGTAGGATGTA[C/T]TTACCATCCTTGAAA	207278
rs31919592	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101167581	ATTTTGTTCCCCCTT[C/T]TAAGAAGAACTGAAG	207278
rs31934564	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101153460	TGGTTAAGAACTCTT[C/G]TTTGTTCTTCCAGAG	207278
rs31948485	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101153408	ACATAAAACATATTT[A/T]AAAAAAAAACTAATT	207278
rs31965898	snp	C/T	0.48	0.0979796	intron-variant	Fchsd2	GRCm38.p3	7:101191225	GTCCTGTACAAGAGT[C/T]GTTCACTAAGCCATC	207278
rs31969060	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101195152	ATGCAAGTGCTCATG[C/T]GCGCGCGCGCGCGCG	207278
rs31971520	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101167835	CCTGAGGACTCAGCA[A/G]TACCACTCCTGGGCA	207278
rs31983478	snp	A/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101147837	AGTTTTTTTTACATT[A/T]AAAAAAAGACTTATT	207278
rs31984186	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101115704	GTTGCTGTCAGGTGT[C/T]ATTCCCATTTTATTT	207278
rs31990736	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101266225	AATTATTTCCTTTCT[C/T]CTGCTTAATTTGGAT	207278
rs31997761	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101279182	GTACCTCCTATAGCC[A/G]GGCAGGACTTATAGA	207278
rs32011093	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101181905	AGGAAAAGAGTCCCA[A/C]GACCAGATACAAGAG	207278
rs32013250	snp	C/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101195844	ACAGACTTTTCTTAC[C/T]CTAAATAAATACTTT	207278
rs32019758	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101182410	CAAACAGTGTTGGGT[A/T]TGGGTTCCTTCTTGT	207278
rs32027652	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101218239	CATCACCTCCCCTGT[A/C]CCCCTGCTCCCCAAC	207278
rs32039482	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101193373	CGCACATCCATGTCA[A/G]CCTCCCATCTCTTCA	207278
rs32042634	snp	A/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101128552	ATGCGTTTGAAATTA[A/T]TGATTTGTTTTTGAG	207278
rs32057876	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101127838	GCAAGGCTGCTAGCA[A/G]TAATGAAATGAACAT	207278
rs32067458	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101128987	CAATAGTAGTATTTA[C/T]TAGGACTACAGGCAT	207278
rs32068184	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101260968	AACCACAGAGGTCCC[C/T]GACTTCAGTCCATTG	207278
rs32070484	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101205159	AGGTTGACAGCTGAA[A/G]CTAACTAGGACAGTC	207278
rs32072428	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101202009	GTCTGTATCCACTAC[A/G]ATAGCCACAGCCTGT	207278
rs32073194	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101250704	TGTAAGTACACTGTA[A/G]CTGCCTTCAGACACA	207278
rs32078302	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101153636	ATGTAAAAGAATAAA[A/C]ACTATTAAAAAAGAA	207278
rs32081792	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101275070	CTGCATCAAAAACAC[C/T]GAAATATTAAAAAAA	207278
rs32082431	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101213641	CTTACAGAGAACCAG[A/G]GTTCAATTCCCAACA	207278
rs32086905	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101281357	TTGTTCTGTCTCAGC[G/T]GCGTCAGCTGAAGCC	207278
rs32087756	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101280381	CATTTAATGAGATGA[C/T]CCCATGACTTTTCTT	207278
rs32092408	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101222425	CAAATAATTCAAAGT[A/G]GGAAGAAAGATAAAT	207278
rs32096096	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101222651	GTGCCATCAGCTAGG[A/G]ACCGAACATCAACAT	207278
rs32101170	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101261475	CACTCCTATCTCCCA[C/T]GCCCCAATTCCTGAT	207278
rs32109992	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101199031	GTAGAACTTTTGAAT[A/G]TCTTCTGAGCCACCA	207278
rs32113968	snp	G/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101171633	GTGCCTCTTTTAAAA[G/T]AGGGTGGCTTTTATT	207278
rs32116082	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101164601	TCAATTACATTTCCA[A/G]TGCTATCCCAAAAGT	207278
rs32116412	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101131700	AGCATCTGTCTTTTT[A/T]AAAGAGAGTATCTCA	207278
rs32116413	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101247416	GACTAGAGGAGCTCA[C/T]TGACGTGGTCACAGA	207278
rs32117413	snp	C/T	0.375	0.216506	synonymous-codon	Fchsd2	Mm_Celera	7:101277627	ATGGACAAGAGAGAT[C/T]CAGGCACGTGCAAAG	207278
rs32118329	snp	C/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101187871	AATGGGATTAAAAGC[C/T]CTGAAGTCATGTAAT	207278
rs32119003	snp	A/G	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101196057	GATGCTGTTAATTGA[A/G]CATAGAGGTTACTAC	207278
rs32122235	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101110299	TGTGCTGTCAGAGTG[A/G]AGGGCATCATTCTGA	207278
rs32128293	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101182322	GAATCATTGTACTTA[A/T]TATTTTTTAGACCAG	207278
rs32149488	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101162298	TGTTCTTTTCTACTC[C/T]CCAGTCCCTTTCACT	207278
rs32162550	snp	A/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101120430	CTCCACCACTGCCCA[A/G]CTGTTTACACTTTAC	207278
rs32164257	snp	C/T	0.375	0.216506	utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101283493	CAGCTTCAGGTCCCA[C/T]TGCCCTGACATTTGT	207278
rs32166711	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101178311	TTGATAAAGACAAAC[A/G]TCATCAGAGCATTTC	207278
rs32166996	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101116217	ATAGCAAGTGTCAGA[C/T]CAGATCAGACTACTG	207278
rs32173268	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101146579	GAAACAAATTTGCCA[C/T]AGTCATGTTTTTTTT	207278
rs32183093	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101254385	TGGCTCACAACCATC[C/T]GTAACAAGATCTGAC	207278
rs32193915	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101157233	GCCTCTTCCTATAGT[A/G]AGTGTCTGGGATTAA	207278
rs32196573	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101130823	TTGTTTGGCGTGCTG[A/C]TTGGTTTCTCAGTTG	207278
rs32201483	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101148213	CCTATTTATTTTTTA[A/C]AGATTTATATTATAC	207278
rs32221567	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101184004	ATCAGCAAAAGAGAG[G/T]GAAGAGTACCTAATG	207278
rs32225862	snp	A/C	0	0	intron-variant	Fchsd2	Mm_Celera	7:101160855	AATGACTTTTGTTCC[A/C]CCTTCTGTAAATTGT	207278
rs32232832	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101146763	AGACATTCCAGAAGA[A/G]GGTGTCAGATCTCAT	207278
rs32235773	snp	G/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101151526	TTTTAAATATTTTTA[G/T]ATTTTATGCATTAGA	207278
rs32241506	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101155676	AACTGTGCTTCAAAC[C/T]TGACTTAATAAAATA	207278
rs32243348	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101281365	TCTCAGCTGCGTCAG[C/T]TGAAGCCATTGAACT	207278
rs32245271	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101256732	CTCCCAAGTGCTTAA[C/T]GTGATTAAAGACATG	207278
rs32261036	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101111500	GCACTAACATTGTGA[A/G]AATGAATGTTATAAC	207278
rs32265612	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101169752	CATTGTTAAAAGAAA[A/G]ACCATGGAACTGGGA	207278
rs32279509	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101199910	TGCTGGAATTAAAGG[C/T]GTGCGCCACCACCAC	207278
rs32284510	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101119693	TTTAAGACAGCGTCT[C/T]TCTACACAGTCCGGG	207278
rs32285347	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101209410	ATCTCAGAAATATGG[C/T]GGAGAGCAATAGAAG	207278
rs32296633	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101117484	ATTTCCACAAGAAGA[C/G]CGAAGATGTGATTGT	207278
rs32314167	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101141981	TCTCACCAGCCCCAC[C/T]TACAGATTTTTAATA	207278
rs32315441	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101219176	GCTTTGCCCCCCCCC[C/T]TTTTTTTTAATGCTT	207278
rs32325062	snp	C/T	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101158289	TCTCCGTATTTCCTC[C/T]CATAAGTATTTTGTT	207278
rs32331737	snp	A/G	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101132409	GCTTCAGAGTAGGTT[A/G]TTGTTTGTTTTGTTT	207278
rs32337140	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101226411	CCAGCCTAGTCTAAT[A/G]AGTGAGTTCCAGGAC	207278
rs32341637	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101138662	TGTCTCCCCAACCTT[A/G]GAGCTACTTATCACA	207278
rs32345071	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101244885	GGAGCTAGAGAAATT[A/G]CCCAAGGAGCTATAG	207278
rs32354850	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101268876	TTGACTGCTCTTCAC[A/G]CTTCCTAGAAATGGA	207278
rs32378265	snp	A/C	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101170383	AAAATGATCTGGATC[A/C]GAGTCTCTGCCTAAC	207278
rs32390063	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101267612	ACACAGCAAGTAAGT[A/G]ATACAGTCAGTATTC	207278
rs32391132	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101116154	AGTCCCAGCACTTGG[A/G]AGGCTGATGCAGGAA	207278
rs32398086	snp	C/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101143231	ACACCTAAAGCTTTT[C/T]TTTTTAAACTATTTT	207278
rs32398575	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101207168	TATATCAGCTGTTAT[A/G]TTTTAGTCTTTTCTT	207278
rs32404788	snp	A/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101157137	TCTGGTAACCAAAAT[A/G]GCTGGGTTATATAGG	207278
rs32405357	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101267193	CACAACAAATTTTTT[A/T]AAATTGTTTCTGGCA	207278
rs32410921	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101183815	CTATACATATTTAAT[A/G]TATGTTCAATAAGTA	207278
rs32415954	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101210219	ACTGGGCGGTGGTGG[C/T]GTACGCCTTTAATCC	207278
rs32416354	snp	A/C	0.265928	0.249492	intron-variant	Fchsd2	Mm_Celera	7:101199169	AATTGTTTTATGAGA[A/C]GATATATTTTATAGT	207278
rs32422515	snp	C/T	0.375	0.216506	upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101107428	TGAGGTTGAGTTTAT[C/T]CAAGTAGTTCAGGAC	207278
rs32429079	snp	G/T	0.5	0	intron-variant	Fchsd2	Mm_Celera	7:101214003	CTCTTCCTCCTCCTA[G/T]CCTTTGGTAAAATAT	207278
rs32433663	snp	G/T	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101199896	ATTTGCCTCGTGAGT[G/T]CTGGAATTAAAGGTG	207278
rs32433996	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101140501	TCAAACCTGAGTCCT[C/T]TGTAAGAGCACCCAG	207278
rs32435574	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101248407	CAAAGAAGAGAACAT[A/G]AACTTGACTGGGAGT	207278
rs32439931	snp	C/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101238413	TCCCGGGCGGCGAGC[C/G]GGAATCCCTGTGAGG	207278
rs32458322	snp	C/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101178310	GTTGATAAAGACAAA[C/T]GTCATCAGAGCATTT	207278
rs32463644	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101272337	CAACAACTAGAGCTC[C/T]CTTTGCCCTTACAGA	207278
rs32475931	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101277247	TCCATCTTGCTAGAC[A/G]CGTTATGGGTACACC	207278
rs32485965	snp	C/T	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101162228	CTTGCATTATAGTGA[C/T]AATCTGTATAATCAT	207278
rs32486112	snp	A/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101268671	CTTACGAATAATCTA[A/T]GTACTCAAAAGAAAG	207278
rs32489018	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	GRCm38.p3	7:101129511	CACTTTCATGGCATA[C/T]GCACAGATACTTATA	207278
rs32497199	snp	A/G	0.444444	0.157135	intron-variant	Fchsd2	GRCm38.p3	7:101279548	GGAGACATCCAGTTG[A/G]ACCAGCACCATTTGT	207278
rs32505970	snp	C/T	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101153605	ACACAGACAAACATG[C/T]AGGCAAAGAACTCAT	207278
rs32507122	snp	A/G	0.375	0.216506	intron-variant	Fchsd2	Mm_Celera	7:101272900	ATGCAAGGGAGGCAT[A/G]AACAAGCGAGGCCTC	207278
rs32512390	snp	C/T	0.32	0.24	intron-variant	Fchsd2	Mm_Celera	7:101170653	GGCTGTTGTCAAGCA[C/T]GAGATACCATTTGCT	207278
rs32513212	snp	A/T	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101242356	AACTAAATGGTAAGG[A/T]ACTGGAAGCAATTCC	207278
rs32516265	snp	A/G	0.5	0	intron-variant	Fchsd2	GRCm38.p3	7:101246142	CAGAAAGTTAGAATA[A/G]TAGTGACTCTTACCT	207278
rs32521071	snp	C/G	0.444444	0.157135	intron-variant	Fchsd2	Mm_Celera	7:101216319	ACACACACTCACACA[C/G]AGAGAGAGAGAGAGA	207278
rs32532964	snp	A/G	0.32	0.24	intron-variant	Fchsd2	GRCm38.p3	7:101272324	TCCCTTGCCAGGTCA[A/G]CAACTAGAGCTCCCT	207278
rs45664362	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101252167	CCATATATAAGTTCT[C/T]TGAAATAACTCTGAG	207278
rs45688325	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101166737	TGGTGACTCTTAGGG[A/T]CAAAGGTGTTTGGCC	207278
rs45808343	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101237961	GTTTACCAAGATCAA[A/G]AACTACCCTCATGAC	207278
rs45942922	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101226437	AGGACAGCCAGGGCT[A/G]TACAGTAGAATTCTG	207278
rs45950256	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101226287	AGGTTCACCAAATTT[A/T]AAAAAAATTATCAAT	207278
rs45981988	snp	A/C			intron-variant	Fchsd2	GRCm38.p3	7:101139868	CCTCAGAATGCTAAG[A/C]TCAGAGGTGGACCAC	207278
rs46021657	snp	A/C			intron-variant	Fchsd2	GRCm38.p3	7:101205836	CCAGGCCATCTTCTG[A/C]TACATATGCAGCTAG	207278
rs46029466	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101265217	GCCAGGCATGGTGGC[A/G]CACACCTTTAATCCC	207278
rs46117199	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101202202	GAGGGCTGTGTCTGG[C/G]TCTGTGGTCCTGTTG	207278
rs46131934	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101224978	TTCATGAGGTGCTGA[A/G]AAGAAGGTATATTCT	207278
rs46214680	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101261091	TAGCATCAGTAATAG[G/T]GTCAGGCCTTGGAGC	207278
rs46221054	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101225104	GGCCTGTCAATTGGT[A/G]GGGTGGTATTGCAGT	207278
rs46228120	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101189472	CTTGATTTTGTGGCA[G/T]TTGTCTGTCTCAGCC	207278
rs46279468	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101225128	TTGCAGTCTCCCACT[A/T]TTGGAGTTCTGTGTG	207278
rs46299036	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101255120	CCTGGCCAGTCGAGC[A/G]CGCGCAAGATGAATG	207278
rs46473166	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101202161	CCACCTGAGGCCATG[A/G]TGACATCCTGGCCCA	207278
rs46492036	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101205908	GTTCCACCTATAGGG[C/T]TGCAGATCCCCCCCA	207278
rs46499505	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101158402	GAACAAATATCTGGG[G/T]TATTCCAAGTTTTGA	207278
rs46778856	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101257059	GTGCTTACCTTTCTT[G/T]CAGGGGACTGGATTT	207278
rs46822466	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101155058	TGAACTTGCCCATCT[C/T]GACAGCAGGCAGCCG	207278
rs46892723	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101122240	TAGAATAGCTTACAG[A/G]CTGTGTCTAGCTACT	207278
rs46930310	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101139478	AAAGATGTGTACCAC[C/T]ATCACTGTCTGATTC	207278
rs46944447	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101155050	GGGTTTCATGAACTT[A/G]CCCATCTTGACAGCA	207278
rs46962685	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101136398	ATGTAAATACACATA[C/T]ACACATTTTTTTTGA	207278
rs46997764	snp	A/C			intron-variant	Fchsd2	GRCm38.p3	7:101232075	TGAAAGGAAATATTT[A/C]CAAATTATTTATCTT	207278
rs47028599	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101267648	CAGCCAGTCAGTCAC[C/T]GCTTCCTGTCTGGGA	207278
rs47515441	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101126861	CTTCTTGAGATCTGG[A/G]ATTACAAGTGTGCAC	207278
rs47526010	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101262442	GCATGTCTTTGACTC[C/T]AGCCCTCAGGTGGCA	207278
rs47642107	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101202169	GGCCATGGTGACATC[C/T]TGGCCCAGGCTGCCA	207278
rs47673645	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101202179	ACATCCTGGCCCAGG[C/T]TGCCACTGAGGGCTG	207278
rs47721849	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101190982	AACTTGATGTAATTT[A/G]TAAATTAATCAAGTT	207278
rs47754864	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101154178	AAGGAATTTTTTTTT[A/T]AAAAATCATAGGAAA	207278
rs47772272	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101205290	ACCTTATAATAAAAT[C/G]GCTTCCTTGTTATGG	207278
rs47802813	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101202170	GCCATGGTGACATCC[G/T]GGCCCAGGCTGCCAC	207278
rs47813462	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101262532	AGTTTCAGACTGTCC[C/T]GGACTATGTAATCAG	207278
rs47951799	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101134470	CAACCATAACCTACG[C/T]AGAGTTAGGTCAGCC	207278
rs48005693	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101257217	ACACACACACACACA[C/T]ACACACACACACACA	207278
rs48018846	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101162575	AAATTAAATATGAGA[A/G]CTAGTAAGTGGCCCA	207278
rs48050906	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101265232	ACACACCTTTAATCC[C/T]AGCACTTGGAAGGCA	207278
rs48062745	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101265801	CCATTTATAGCCCTT[A/G]CTGGCCTAGAACTCA	207278
rs48122419	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101197394	GTTCAATTCCCAGAC[G/T]CTACATAATGGAAAG	207278
rs48143583	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101219345	AATATCATCATATTG[A/G]TGAAATGTTTACTTA	207278
rs48145307	snp	A/C			intron-variant	Fchsd2	GRCm38.p3	7:101205942	CCCTGGTACTTCCTC[A/C]AGCTCCTCCATTGGG	207278
rs48519229	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101262270	CTTAGTCTCCCTGTC[C/T]TAGAGAACCATATTT	207278
rs48558712	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101172221	CATCTCCCCCTCCCC[C/T]GCTTCTATGAGGGTG	207278
rs48615347	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101202194	CTGCCACTGAGGGCT[A/G]TGTCTGGCTCTGTGG	207278
rs48631971	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101246802	ATTTTTTTAATAATG[A/G]AAGAAGTTAAATTCA	207278
rs48668174	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101116849	ACATGGTGTAATGTA[C/T]CATGTCTCTAATCCT	207278
rs48677621	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101262264	AAACCGCTTAGTCTC[C/T]CTGTCTTAGAGAACC	207278
rs48691501	snp	C/G			intron-variant	Fchsd2	GRCm38.p3	7:101187381	CCAGTTTCAGACCAG[C/G]CTGGTATACATAGTG	207278
rs48807575	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101262439	GCTGCATGTCTTTGA[C/T]TCTAGCCCTCAGGTG	207278
rs48914663	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101135914	ATGTTACTTGGACAA[A/T]TTTTTTTTTTTTAAG	207278
rs49274818	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101189560	AGTTCATATTCTGGG[A/G]TCTGGAGAGTTTGCT	207278
rs49349352	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101265110	TTAACCACTGATCTA[C/T]TTTCTGCACTTTAGG	207278
rs49392225	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101189222	GTTCCTTGTCCCATT[A/G]GGGTCTGGGTTGGGA	207278
rs49398022	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101135943	AGATTTATTTAATGT[A/G]AGTACACTGTAGCTG	207278
rs49412029	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101130379	CCCAGTGATTCCCCG[A/T]TTCCATCTCCCCAGG	207278
rs49412700	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101134308	ACTAAACATAGCATA[C/T]CAGATTGCAGTAAAA	207278
rs49449151	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101225370	GAGATGACTCAATTG[A/G]CAAGGGTATTTGCAG	207278
rs49583836	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101202188	CCCAGGCTGCCACTG[A/C]GGGCTGTGTCTGGCT	207278
rs49741963	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101271014	GCAACCACATGGTGG[C/T]TCACAACCATCCGTA	207278
rs49806800	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101208565	GCCTCCCAAGTGCTG[G/T]GATTAAAGGTGGTGT	207278
rs49854701	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101252392	TGCTGGATGTCTCAC[A/G]TTCTAATCCTGCCTC	207278
rs49912549	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101267649	AGCCAGTCAGTCACT[G/T]CTTCCTGTCTGGGAG	207278
rs49940050	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101201173	TTTTTTTTTTTTTGG[G/T]AAATGTAATTATATG	207278
rs49940245	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101189414	ACAAAAATCTCACTG[A/T]ATACCTCTAGCTGGC	207278
rs49963122	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101240028	ACCATGTGTACTCTT[C/T]GGTTGGTGGTTTAGT	207278
rs49994846	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101189615	CTTGGAAAGGATCTG[A/G]GTTTGATTCACTATG	207278
rs50057533	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101265270	GCCGATTTCTGAGTT[C/T]GAGGCCAGCCTGGTC	207278
rs50133839	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101151279	AATACATATCTAAAT[G/T]ACTATAGTATGAGAC	207278
rs50231885	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101151038	ACTTCATGTAATTTA[G/T]CAGAATTATACTCTT	207278
rs50307980	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101201443	TGAATGGGTGCCTTA[A/G]AAGCAGGGGATTTAT	207278
rs50357677	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101211498	GAGAGTTGTAACTTT[A/T]AAAAAAAAAGGGACA	207278
rs50414188	snp	A/C			intron-variant	Fchsd2	GRCm38.p3	7:101127303	TTACTTAAGGAAAAG[A/C]GATTACCCTCAATGA	207278
rs50514945	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101262747	ATCTTTAAAATTGTT[C/T]CAATATAATAAGGAA	207278
rs50558143	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101224458	TAAGGGTTTATCTAT[C/T]TTGTTGATTTTCTCA	207278
rs50618177	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101153643	AGAATAAACACTATT[A/T]AAAAAGAAGCGATTA	207278
rs50621952	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101202177	TGACATCCTGGCCCA[G/T]GCTGCCACTGAGGGC	207278
rs50803984	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101154966	GTCCGAGGTGCCATC[G/T]TCAATGTTCTTCACG	207278
rs50820411	snp	C/G			intron-variant	Fchsd2	GRCm38.p3	7:101205364	ACAGAAAATTTTATT[C/G]CCAGAAATAAATGTT	207278
rs50821175	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101255404	CCTTAACATCACCAA[A/G]CTGCTCCACCTCACT	207278
rs50905379	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101165468	GTAAGCGGCACTCCT[C/T]CTTGGCTTCTGTATC	207278
rs50907442	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101168783	TTTCTAATTCATTTT[A/G]TTGAAATTGAAAAGC	207278
rs51083341	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101274505	GGAAGTGTCAGAACT[C/T]CTGGAGCTAAAATTA	207278
rs51093942	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101201446	ATGGGTGCCTTAGAA[A/G]CAGGGGATTTATTCA	207278
rs51131645	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101200522	CATATATCCTATATG[A/T]ATCTACTGTTAGACC	207278
rs51159068	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101255096	GGATCCTGTTGCAGC[A/G]TCGTTCTTCCTGGCC	207278
rs51240216	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101162534	ATCTGTCAACTGAAA[A/G]TATTTTCCTTATTTT	207278
rs51501649	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101206196	GCCTGGAACTTGCTA[G/T]GTAGACCATTGGCCT	207278
rs51526627	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101189339	CTTTCAGAGCATGTG[A/G]CTGCTCTGACCCTCT	207278
rs51623895	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101189598	TATGAATACTTGTTG[C/T]TCTTGGAAAGGATCT	207278
rs51755306	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101163246	CATGTTTCTGAATTG[C/T]CAGTGGAGGCTTAGG	207278
rs51827194	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101255403	ACCTTAACATCACCA[A/G]GCTGCTCCACCTCAC	207278
rs51827523	snp	A/C			intron-variant	Fchsd2	GRCm38.p3	7:101136151	TCAGTAAAGCATTCA[A/C]AAGCATGAGGACCTG	207278
rs51843515	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101208547	AGAAATCCGCCTGCC[C/T]CTGCCTCCCAAGTGC	207278
rs51888889	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101195416	TTAACCAACTATGCC[A/G]TCTCCCCAGCCCCAG	207278
rs51950760	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101274242	TAAACACCTCTATTT[A/T]CCAGTAGGGGTTTTT	207278
rs52005937	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101265209	CAGTGTAAGCCAGGC[A/G]TGGTGGCACACACCT	207278
rs52101879	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101225513	ATGGATGGATGGATG[A/G]ATGGATGGATAGGTA	207278
rs52158973	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101205779	TACTGAGGCATATAA[A/G]GTCTGCACGACCAAT	207278
rs52165629	snp	A/C			utr-variant-3-prime	Fchsd2	Mm_Celera	7:101284273	TCTCCAGGCCGAATA[A/C]CCCGGCGTCACCATG	207278
rs52213976	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101122956	TCACAAAACTTTATA[A/G]GCTATTTTTATTAAA	207278
rs52241029	snp	C/G			intron-variant	Fchsd2	GRCm38.p3	7:101137843	ACACACACACACACG[C/G]ACAGACAGACAGACA	207278
rs52242834	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101256578	CTTGGGTTTTTTTTT[G/T]TTGTTGTTGTTGTTG	207278
rs52248459	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101219914	ATTTATTTATTTATT[C/T]ATTTATTTATTCATT	207278
rs52263424	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101195163	CATGTGCGCGCGCGC[A/G]CGCGTGTGTGTGTGT	207278
rs52283435	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101219922	ATTTATTTATTTATT[C/T]ATTCATTCATTCATT	207278
rs52292230	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101220128	TAAGTAAAGACCATA[C/T]ATATATAAAGACTAT	207278
rs52299444	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101254873	AGTGGCAGTTGCAGA[A/G]TGGCAGTTGCAGAGT	207278
rs52300380	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101265305	AAGTGAGTTCCAGGA[C/T]AGCCAGGGCTACACA	207278
rs52319728	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101225474	ACTTCCATATGTACA[A/T]TATAGCGTGTGCATG	207278
rs52338541	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101189756	ACACATGCATAAAAT[A/G]TAAATATATATATCT	207278
rs52357866	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101201226	GTGTGGGTTTTGGGG[G/T]GTGTGTGTGTGTGTG	207278
rs52363717	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101219983	AGAGCTGTCTGTCCT[A/G]GAATTCACTTTGTAG	207278
rs52381896	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101265393	TTTTGAGGATCACAA[A/G]TGTTGTTGTATGCTG	207278
rs52387674	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101195168	GCGCGCGCGCGCGCG[C/T]GTGTGTGTGTGTGTG	207278
rs52485101	snp	A/C			intron-variant	Fchsd2	GRCm38.p3	7:101219873	TCCAGGTGCCAGATT[A/C]TATTTATTTATTTAT	207278
rs52485329	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101205773	CCCCTGTACTGAGGC[A/T]TATAAGGTCTGCACG	207278
rs52520874	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101137842	CACACACACACACAC[A/G]CACAGACAGACAGAC	207278
rs52526200	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101205782	TGAGGCATATAAGGT[C/T]TGCACGACCAATGGG	207278
rs52533979	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101205698	CTATCCCAAAAGTCC[A/C]CCACACCCTCCCACA	207278
rs52534093	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101123299	CCTGTCATATTTTTT[C/T]CTCCCTTTCTCCCTC	207278
rs52574041	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101219875	CAGGTGCCAGATTAT[A/T]TTTATTTATTTATTT	207278
rs52592478	snp	C/G			intron-variant	Fchsd2	GRCm38.p3	7:101205771	TTCCCCTGTACTGAG[C/G]CATATAAGGTCTGCA	207278
rs107624685	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101151552	TTAGAAAATTTAACT[G/T]TTAAAAGTGGAATTC	207278
rs107675126	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101111172	GGACAGCCAGGGATA[C/T]ACAGAGAAACCCTGT	207278
rs107746574	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101137856	CGCACAGACAGACAG[A/G]CAGACTGACTACAGA	207278
rs107835092	snp	A/T			utr-variant-3-prime	Fchsd2	GRCm38.p3	7:101283492	ACAGCTTCAGGTCCC[A/T]CTGCCCTGACATTTG	207278
rs107925302	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101224471	ATCTTGTTTATTTTC[C/T]CAAAGAACCAGCTCT	207278
rs108003233	snp	A/T			intron-variant	Fchsd2	GRCm38.p3	7:101219879	TGCCAGATTATATTT[A/T]TTTATTTATTTATTT	207278
rs108044320	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101240476	tgaattgtatcttgg[A/G]tattctgagcttctg	207278
rs108181985	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101241074	TGCTTCTCAGCCGTT[C/T]GGTATTCCTCAGTTG	207278
rs108200108	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101241107	AATTCTCTGAACCTC[A/G]TTTTAATAGGGTTAT	207278
rs108204621	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101120314	TCACAGGGTTTCTCT[A/G]TGCAGCCCTAGCTGT	207278
rs108312345	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101111166	GTTCCAGGACAGCCA[A/G]GGATACACAGAGAAA	207278
rs108356285	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101212440	TGGGTCCTCCATTCT[A/G]TTCTATTGCTTTATG	207278
rs108499059	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101240790	TGGGTATATGCCCAG[A/G]AATGGTATTGCTGGG	207278
rs108600329	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101233471	TTCTACCACTAATGG[A/G]GGAGACTTGTGTTTA	207278
rs108662690	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101163190	TTTGAGCTTCGGGCC[G/T]CTAAATGCTGTGATT	207278
rs211715306	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101199802	TTGATTTGTTTTGAG[C/T]CAGGGTTTCTCTGTG	207278
rs211718929	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101185307	TTGTCAGGCAGGGAG[A/G]CCATGGAAGACTGCT	207278
rs211724401	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101111126	CAGATTTCTGAGTTC[C/G]AGGCCAGCCTGGTCT	207278
rs211760405	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101282096	ATCCTGGTTTCTTAC[G/T]AAAACTTAATAAGGC	207278
rs211776185	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101186867	CTTTTTAACTGAAAT[A/G]TTTTGTTAGCTGATA	207278
rs211847502	in-del	-/AA			intron-variant	Fchsd2	Mm_Celera	7:101183689	TTGTGGGATTGAAAG[-/AA]AAAAAAAATCAGTGT	207278
rs211848027	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101212050	GTTGTGCCCATGTAA[A/G]TTTAATCTAGATTCT	207278
rs211848215	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101198913	GATTTGCAAGGTAGA[A/G]GATGGGTGTATAAGA	207278
rs211850014	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101122655	AGCTTAATAATTTAG[A/T]CTTGAGTGGAGGATT	207278
rs211885339	snp	C/T			intron-variant, upstream-variant-2KB	Fchsd2	Mm_Celera	7:101109964	CTTATGAGTAACTCA[C/T]CATCTATGCTTCCCT	207278
rs211916739	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101242070	CTGTTTATTCTTTGT[A/G]TAGAGGAAGGCCACT	207278
rs211916991	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101258785	TATGTTGGGGTGTGT[A/G]GTCACAGGAGCATAG	207278
rs211938393	in-del	-/AGGGCATAC			intron-variant	Fchsd2	Mm_Celera	7:101242936	ATAAAGGATGAGTGA[-/AGGGCATAC]AGTGGCTAAGTAGAA	207278
rs211940487	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101147571	CAGTTTAGACTTCTA[A/G]CCTCCGGAACTGGGA	207278
rs211955624	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101161489	AATCCACTTGTAATT[A/G]ATATAATCATATATG	207278
rs211985438	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101243481	TGAGATGGGTTCTCA[A/G]TACCCATCTCAGGCT	207278
rs211988735	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101169473	AAGTTTAATTTTTGT[A/G]CAAAAAATGGAATTT	207278
rs212007592	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101159968	GGAAAGAGAGGCCCG[C/T]TGGACACACAAACTT	207278
rs212041531	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101269957	GCAGTCTTCGATGTT[C/T]CCTCATGTTAGCATT	207278
rs212054452	in-del	-/GGTGTGTGTGTGT			intron-variant	Fchsd2	GRCm38.p3	7:101201226	GTGTGGGTTTTGGGG[-/GGTGTGTGTGTGT]GTGTGTGTGTGTGTG	207278
rs212060523	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101257125	TCTATAACTCTGGTT[C/T]AAGGGAATCTGATGC	207278
rs212081046	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101228446	TAGAATTCCATTTCT[C/G]ATTTTGTCTTTATGA	207278
rs212100430	snp	A/C			intron-variant, upstream-variant-2KB	Fchsd2	Mm_Celera	7:101109658	TTAACCCCCACCCCC[A/C]ATCCCTTTTGCCCCG	207278
rs212104285	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101227980	GGTTAATTTTTTTTT[-/T]ATTTACTGTTACAAT	207278
rs212145142	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101268827	ACTCCCATGAGCCAC[C/T]TTCAGTCCCAATAAA	207278
rs212182953	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101201850	GGTAGAAAATAGGGA[A/G]TACCCAGTGGAGAGA	207278
rs212213504	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101172513	CAGATGATAGAAGCA[A/C]TATTACTCAGTGTTG	207278
rs212250931	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101148726	GAACTCATGTCTTCT[G/T]CAAGAGCCGGATGTA	207278
rs212286522	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101136248	AAGTAGAGACAGGAG[A/G]ATCCCTGGGCTTGCT	207278
rs212314238	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101162067	CCTTGTCTCACATGT[A/G]CAGCTTTTTCTCCTG	207278
rs212332554	in-del	-/AA			intron-variant	Fchsd2	Mm_Celera	7:101113343	CTGTCTCGAAAAACC[-/AA]AAAAAAAAAAAAAAA	207278
rs212346693	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101125592	TTGTGTATGTGTGTG[C/T]GCTCAGGAGCAAACA	207278
rs212347608	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101127026	AGAACTGGTATGGTA[A/G]CACATGCCTTCAGTT	207278
rs212348372	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101214148	AGGAAGCATATGGGG[-/T]TTTTTGTGTGTGTGT	207278
rs212376238	in-del	-/GG			intron-variant	Fchsd2	Mm_Celera	7:101145798	TGTGGAGGTCAGAAA[-/GG]GGGGTATCAGATCCC	207278
rs212394339	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101190863	AACAATTTACATAGG[A/G]ATATATTGTATTTTA	207278
rs212450777	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101202961	GAAGTTGCAAGGGGG[A/G]ATGGGGGATGAATGG	207278
rs212458751	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101164499	CTTCCTTTTTTCCCT[C/T]TAACCTTTCTCATTT	207278
rs212469244	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101227487	TATTATTGCCATCTT[C/T]TTTATAAGTAACATT	207278
rs212480286	snp	A/G			downstream-variant-500B	Fchsd2	Mm_Celera	7:101284902	TCTTTCTTTGTTTTT[A/G]TCATTGTCTTTTTGA	207278
rs212534778	in-del	-/C			utr-variant-3-prime	Fchsd2	Mm_Celera	7:101284071	GAGCAGTTCCTGCTA[-/C]CCAGTCCTGTATTCT	207278
rs212539535	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101247792	TTACATGCAGTATGT[A/G]TAGTCTTCTTTCTTT	207278
rs212545129	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101150468	CCATCTCACTATGGG[C/T]GGTGCCATTCTGGGC	207278
rs212557838	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101273392	TGCTGATATATCCAG[C/T]CATTTTCCTATGGTA	207278
rs212560015	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101120825	TGGCTCTGCATTGTC[-/T]TTTTTTTTAATCTGT	207278
rs212598849	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101177496	ATTCTATGTACCGAC[A/G]TTCGTATGGCATGTA	207278
rs212605882	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101230359	AGAAGGACAGGCAAG[C/T]GTCAGAAGCACAAGA	207278
rs212607021	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101176229	GCTAAGGAAGAAATA[C/T]CAATTAGGTTCCCTA	207278
rs212617937	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101261643	CAGTTCTATGGATTG[A/T]ATCCTGGGTATTCTG	207278
rs212657294	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101112841	GCATGCACCACCACA[A/C]TTGGCCTGCCGCTTA	207278
rs212730640	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101205748	ACTCCCACCTCTTGG[C/T]CCTGGCGTTCCCCTG	207278
rs212760146	in-del	-/TGTGTGTGTGTGTGTGTGTGTGTG			intron-variant	Fchsd2	Mm_Celera	7:101138210	TCCCACTTGTTTAAC[-/TGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT	207278
rs212766329	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101272473	TTAAAATAAGTAATC[-/T]TTTTTTAAAAAAAAA	207278
rs212812110	in-del	-/CAG			intron-variant	Fchsd2	Mm_Celera	7:101135869	TGATGGGATACTATT[-/CAG]CAGTTAAAAATAGAT	207278
rs212835569	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101152799	GACTAATTATAATTA[A/C]TGTTCTGATACCCTT	207278
rs212870535	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101231420	TTCATAACTATTTGA[A/G]GTTTATATTTAAGGC	207278
rs212871908	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101140367	TTTTGCCTTCTTGTA[A/G]TTGTGTGTATTATGT	207278
rs212894217	in-del	-/CACACACACACA			intron-variant	Fchsd2	Mm_Celera	7:101216292	TGGAGACCTTGTCTT[-/CACACACACACA]CACACACACACACAC	207278
rs212895886	in-del	-/A			intron-variant	Fchsd2	Mm_Celera	7:101268234	AAGAAAGGTCTTCTG[-/A]AATATATAAAATATG	207278
rs212899689	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101194215	TATTTCCCAGTAGAG[C/T]CTGGGAGATAGCTGA	207278
rs212899762	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101178808	GCTTCAGAGTTCCTC[A/T]TGTATCGAGTTAGAG	207278
rs212953351	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101163256	AATTGTCAGTGGAGG[C/T]TTAGGTGACGTTGGA	207278
rs212957444	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101116610	TGGAAACATTATACC[C/T]GATCTAGTGTGATAG	207278
rs212960789	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101179918	TCCACTTATCTATTG[C/G]TGTTGTCCTTGTTCA	207278
rs213027040	in-del	-/A			intron-variant	Fchsd2	Mm_Celera	7:101160379	AATTAAGGGGGAGAG[-/A]AAAAAAATCCCCAAC	207278
rs213041311	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101270736	GTTTTACTTTATTGG[G/T]GTGTGTGTGTGTGTG	207278
rs213055206	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101231505	AGCGGGGGGGGGGGG[G/T]AGGAGATAGGAGATT	207278
rs213100791	in-del	-/C			intron-variant	Fchsd2	Mm_Celera	7:101183256	AATGATATTTTTTTT[-/C]TAACTCCATCCATTT	207278
rs213128803	in-del	-/AA			intron-variant	Fchsd2	Mm_Celera	7:101272480	TAAGTAATCTTTTTT[-/AA]AAAAAAATGTCTTTC	207278
rs213198277	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101235497	ATATAAACCAGGCTG[C/T]CCTTAAACTCACAGA	207278
rs213209242	in-del	-/AG			intron-variant	Fchsd2	Mm_Celera	7:101179526	TTTGGAAGAGACAGT[-/AG]AGAGGTCAGAACTGA	207278
rs213230707	in-del	-/AAAC			intron-variant	Fchsd2	Mm_Celera	7:101200982	CAATAAAAAATAAAA[-/AAAC]AAACAAAGAAACAAA	207278
rs213247459	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101217378	GCCTACTCAGCCTGG[A/G]TAGACTTATACTTAA	207278
rs213258783	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101251764	GAAATCAAGTTTTAA[A/G]AATTTTGTATCAGCA	207278
rs213268674	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101153912	CTGTACCATTAGATG[C/T]CAGAAGCATTGCTTG	207278
rs213288337	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101176024	CAACCTATAAATAAA[A/G]TATAATAAATTACTT	207278
rs213400332	in-del	-/A			intron-variant	Fchsd2	Mm_Celera	7:101236488	CAATGACTAGACTGT[-/A]AAAAAAACAAAAGTA	207278
rs213412613	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101113686	GTTTCTCTTTCTAGT[C/T]TTTCTGTTTTGTTTT	207278
rs213415123	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101270653	GCTCCATCACTGCCC[A/G]GCTGCCAGCCTTGAA	207278
rs213440658	in-del	-/GCGTGT			intron-variant	Fchsd2	Mm_Celera	7:101216341	AGAGAGAGAGAGAGA[-/GCGTGT]GAGCGAGCGAGCTCG	207278
rs213470395	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101272207	ACCCAACTCCTGCCC[C/T]CTGAACATCTTTGTA	207278
rs213472752	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101259287	ATTCTCATTTCTTCC[G/T]AGTCACATTTTGTTT	207278
rs213481841	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101189517	TTACAGGCATGCAAT[A/G]TGCTCCAGCTTATCT	207278
rs213508977	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101275482	GAGTATTATGAAGGG[G/T]CCTTCATCTTCAGTC	207278
rs213509432	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101117817	AAAAAAAAAGAAGAG[A/G]CAGGCAGATTTCTGA	207278
rs213549668	in-del	-/TTTTT			intron-variant	Fchsd2	Mm_Celera	7:101148134	AGCCCCATTTTTAAG[-/TTTTT]TTTTTTTTTTTTTTA	207278
rs213570687	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101217239	ATATAAACGATGAGG[A/G]AAACAGGCTAAGCCA	207278
rs213594491	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101155131	AACCTTTCACCTTAC[A/G]GAGAGGTGGCTTCTT	207278
rs213599573	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101230033	TTTGTAATAATAAAA[A/G]GGAAAAAGAAGGCAA	207278
rs213608198	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101164265	TGCTTGAGTGCTGCC[A/G]TGCTTCTCACCATGA	207278
rs213618459	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101149423	GTTGTTGTTGATGTG[C/T]CCATTTATTGGTTTA	207278
rs213638653	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101138930	AGTATATTCCTACAT[A/C]ACAGCTTCCAGGGGC	207278
rs213653617	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101150024	ATTCTAGTCAGAGGA[G/T]CTGATGTTCTCTTCT	207278
rs213749569	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101168789	ATTCATTTTATTGAA[A/G]TTGAAAAGCAATGAA	207278
rs213757072	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101125175	ATATTTCCGTATTTA[-/T]TTTTTTCCATTCTTT	207278
rs213795436	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101143884	TTCGACTTCTATTCC[-/T]TTTTTTCTCCAGAAC	207278
rs213825506	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101218022	TAGGCCCTGTTCCTA[C/T]CCTCTGCTCCATTCT	207278
rs213831006	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101204160	AGCCTCATACTCACT[A/G]TGTAAATAAGTCTAG	207278
rs213852101	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101115321	AGTGACTCTCCCTGT[C/T]CTATGTGTTAATCCA	207278
rs213872297	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101167156	GTTTGTCTAACTTCC[C/T]GCCAGGAGATCTCTC	207278
rs213901960	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101192808	AAAACATTTGCATAA[A/G]GTCTTACAAGGTGGG	207278
rs213909586	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101263863	TCCAGTGGAATTTGT[A/G]TTTAAATTATGAGAA	207278
rs213911634	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101249158	GTTATTTTTCTTCTT[A/G]TTATAGATTCTTTGT	207278
rs213912509	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101152999	TTGCACAGGCTGGCC[A/G]TAGATTCCTGGACTC	207278
rs213923176	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101127864	AACATTGCTTATATA[C/T]ACTAGAAACCACCAT	207278
rs213929303	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101174177	AAAGTCTTTCATCTA[G/T]AGAGCTCACTGTTTG	207278
rs213997210	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101119301	TAATAGCTGGCACAC[C/T]GTGCCCCATTTATAC	207278
rs213999019	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101219392	TAAAATTAGGTTGTA[-/T]TTTTTTACTGAATTA	207278
rs214006697	in-del	-/G			intron-variant	Fchsd2	Mm_Celera	7:101158196	ATAGTGTCTAGGTTT[-/G]GTTTCTGCATGTGGG	207278
rs214065324	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101127320	ATTACCCTCAATGAA[A/G]TTATTAAGCCTTATT	207278
rs214120283	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101246584	ATTCTTCATCCTCTC[C/T]AGAGCACCTTAACTT	207278
rs214131903	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101206956	TACCTCATTAATAAA[C/G]CAGCAGTATAGATTC	207278
rs214143349	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101251288	ACATGTGTGCCTGAC[A/C]CAGAGGTCAGAAGAG	207278
rs214198057	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101228697	CTATTCCTATGTCCT[G/T]ACTTAAGGCTTATGG	207278
rs214213922	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101137629	GTTTATAAGGAAGAA[A/T]TGTTATTTTTTAACC	207278
rs214251267	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101196286	CTTAATACTAAGGCA[C/T]AGCTGCCAGCACATG	207278
rs214256022	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101178620	GTAAACCTAGCAGTG[C/T]GTGTGGAGAATACAT	207278
rs214268345	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101191314	TGCTTAAAGCAGACT[G/T]TATGTTAGGAGTGTG	207278
rs214274282	in-del	-/CCA			intron-variant	Fchsd2	Mm_Celera	7:101181902	AACAGGAAAAGAGTC[-/CCA]AGACCAGATACAAGA	207278
rs214289696	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101273838	AGATAAGTGAGACTG[A/G]ATTTCTGACTTATTG	207278
rs214316757	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101197049	CACTTTAATATCAAT[A/G]ACCCAAGCAAGAGCT	207278
rs214331393	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101118264	TGATCTACTAAGGAG[A/C]TCCAGGCTGTCTAGC	207278
rs214363264	in-del	-/ATT			intron-variant	Fchsd2	Mm_Celera	7:101243615	TTAAAAATAAAACAA[-/ATT]ATTGTTTGTTTATCT	207278
rs214371026	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101219993	GTCCTAGAATTCACT[C/T]TGTAGACTAGGCTAG	207278
rs214400536	in-del	-/TT			intron-variant	Fchsd2	Mm_Celera	7:101250664	GGGAGCTTCACCTAA[-/TT]TTTTTTTTAAGATTT	207278
rs214461463	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101128774	TGTGCTATTTAATTG[C/T]ACCAGGTGTAAAGTG	207278
rs214475769	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101179639	CTCTCCAAATCTTCC[C/T]GTACTACCCTTCCAT	207278
rs214484903	in-del	-/CCTAGTACTCAGAGATCTT			intron-variant	Fchsd2	Mm_Celera	7:101199857	TGTAGACCAGGCTGG[-/CCTAGTACTCAGAGATCTT]CCTGCATTTGCCTCG	207278
rs214490558	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101156472	AACCAATCACCCACT[A/G]GAATACATTGGCTCT	207278
rs214534578	snp	G/T			upstream-variant-2KB	Fchsd2	Mm_Celera	7:101108388	GCGGCCTGGCTAACC[G/T]CCCCCCCTCCACTCT	207278
rs214537018	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101141771	GGTCAGATGTCCATT[C/T]TTTATTGTCACTTAC	207278
rs214618595	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101279168	AGAGACTGAAGTATG[C/T]ACCTCCTATAGCCAG	207278
rs214652097	in-del	-/GTGTGTGT			intron-variant	Fchsd2	GRCm38.p3	7:101122186	GAACCTACAGAATGA[-/GTGTGTGT]GTGTGTGTGTGTGTG	207278
rs214676867	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101276212	TGCATGTCCATTCAA[C/G]TGTCTTCTCTGTTAC	207278
rs214737705	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101235154	GTTGCACATAACACA[C/T]GCATACAGGCAAAAC	207278
rs214745269	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101158153	AGCTATATCAGGTTC[C/T]TGTGAGCATGTACTT	207278
rs214777920	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101143128	AAGAACAGGAAAAGA[C/T]TGTGGACTTTTAAGG	207278
rs214789902	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101146109	ACTTGGGAGGCCTAG[A/G]TAGGAAGATCTCTGA	207278
rs214805047	in-del	-/AACA			intron-variant	Fchsd2	Mm_Celera	7:101133822	GACAAGACTTTATCT[-/AACA]AACAAACAAGCAAAC	207278
rs214811175	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101221875	TATTTCCCTTACTAC[A/G]CACATGCAGTATACC	207278
rs214864572	in-del	-/GA			intron-variant	Fchsd2	Mm_Celera	7:101271331	CTCACTATGTAGCCC[-/GA]GTAAATGGTCTGAAA	207278
rs214865220	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101231588	ATATCTAATTAAAAT[A/T]TTTTAAATATATTTA	207278
rs214889855	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101238308	AAGGGGAGCTCGAGC[C/T]AGAGCAGGACTTCGG	207278
rs214928138	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101233235	AATTGATGAGAAGAG[A/G]AAAATGTAGATTTTT	207278
rs214947015	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101169041	GTGACATCTTTTTGT[A/T]AGCAATTATTTATGT	207278
rs215045091	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101118051	CCTGCAAGTTTTCCT[C/T]TGTCTTCCACATACA	207278
rs215056850	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101131393	CTGCCAGTCATCTCA[C/T]GAGGCTGTCCCCCTT	207278
rs215070385	in-del	-/TCT			intron-variant	Fchsd2	Mm_Celera	7:101213387	TGTGAACTGGTGAGA[-/TCT]TCTTTACCCATCTGC	207278
rs215110244	in-del	-/ACTT			intron-variant	Fchsd2	Mm_Celera	7:101247641	AGTAAATCATAAAAC[-/ACTT]ACATGACCATGAGAA	207278
rs215113902	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101150341	TAGTTGTGTGGTTGG[-/T]TTTTTTTTCGTGTGT	207278
rs215173694	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101219826	TGGATCCTCTGCAAA[A/G]TCAGCCATGCTTTTA	207278
rs215190449	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101223698	TCATCTGTGAACAGT[A/G]ATACTTTCACTTCTC	207278
rs215193193	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101169914	CAGGCAGGAGTGGAG[A/G]CACCAGAAGGCTTGG	207278
rs215200352	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101130047	CATGAAACTATAATA[C/T]TTTTCTATTTTGAAT	207278
rs215211919	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101168077	AGAAAATAGCATCCT[C/G]AGTGAGATAACCCCA	207278
rs215218375	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101132972	AAATGATTAAGGTTA[A/G]TGGGGAAGGCATCTT	207278
rs215268197	in-del	-/A			intron-variant	Fchsd2	Mm_Celera	7:101162696	ATAATATAATTATAT[-/A]AAATCATTTATGAAT	207278
rs215274161	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101168922	TTTTTGTAAATACAT[C/T]ATATTATTGATATAA	207278
rs215276372	in-del	-/G			intron-variant	Fchsd2	GRCm38.p3	7:101145631	AGAGGGTGGATGGGC[-/G]GGGGGGGGGGGTTAG	207278
rs215310798	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101280209	CTTGCCCCTGATTTT[A/C]GTGGAATTGGTTTAA	207278
rs215343756	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101180464	TCTTTCTGCCAGAAA[A/G]TGTGCATATGCCTTC	207278
rs215365371	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101262545	CCCGGACTATGTAAT[C/T]AGACTCAATCTGAGA	207278
rs215365523	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101183799	TTATGTATCCAAAGT[C/T]CTATACATATTTAAT	207278
rs215382526	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101279068	GGAAATCTGTGGAGA[C/T]AACTCTGATAATAGC	207278
rs215383926	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101264198	TCTTCTTTTTAAAAG[C/T]GTGCTGAAAATGTAG	207278
rs215391995	snp	A/C			intron-variant	Fchsd2	GRCm38.p3	7:101266499	TAGATTTCTAATTCA[A/C]TTATGTTGTAGATCA	207278
rs215407087	in-del	-/G			intron-variant, upstream-variant-2KB	Fchsd2	Mm_Celera	7:101110194	AGTGGGCTGCCACCC[-/G]GCCTGGCTTGCTGGG	207278
rs215434571	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101222213	ACTTGAAGTATTGAG[A/G]ACCAGCTCCAGACTT	207278
rs215440093	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101249029	TTGGTTTGTAATTAC[C/G]TGATAACCAGCTGTT	207278
rs215450525	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101152913	TTCTTTTGGTCAATG[C/T]TAAACTACATTTTGG	207278
rs215460012	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101131421	CTTCTCCTCAGCCTG[C/T]CATCTCACGAGGCTG	207278
rs215472054	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101131573	AGTCCCACCTTCCTC[A/G]GAGACTTGAAGCTCA	207278
rs215490894	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101223663	CAGAGTTTTTGGGGC[C/T]ACTTATGTATACTAT	207278
rs215494108	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101206763	GGTTTTATGCCTCTG[G/T]CCTCACAAGAATTAA	207278
rs215521321	in-del	-/CCTCATTT			intron-variant	Fchsd2	Mm_Celera	7:101214246	GCTATACTGGGTTTG[-/CCTCATTT]CCTCATTTCCTCTTA	207278
rs215560683	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101210880	AGTAAAGAGAGACCT[A/G]GAATTATTACCTTCA	207278
rs215588459	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101194617	AAGCCTTTATAGAAG[C/T]GGTAATGTTTGAACA	207278
rs215609633	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101280497	ATGTTCTTAATGTGT[C/T]CTTGGACTTGATTTG	207278
rs215613157	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101122552	TATTAACTTACAAGA[C/T]ATTACTTAATAGATC	207278
rs215666063	in-del	-/TGT			intron-variant	Fchsd2	Mm_Celera	7:101224372	GATTTCCTCATTGTC[-/TGT]TGTTGTCTCCCTTTT	207278
rs215674304	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101132823	TTTCATAACTATTGT[A/G]TGTGTTCTGACTGCT	207278
rs215705378	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101209553	AAAGAACAAATTTGG[G/T]TTTTTTTGGGACAGT	207278
rs215754125	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101121058	TTAGTTACAATTTGT[A/G]AATGACTGAAGTAAC	207278
rs215765321	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101171197	CAATGCTTTGTGGAA[A/G]AAAATGTACTAAATA	207278
rs215827350	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101158599	TGTATGAAAGACATT[A/G]AACACACTGTAGTGC	207278
rs215827969	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101172313	AGAGCCTCCACAGGA[A/G]CAAGGGCCCCCCCTT	207278
rs215841583	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101247884	TGAGTAATATTTCAT[C/T]ATATGAATATTCCAT	207278
rs215892862	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101151049	TTTAGCAGAATTATA[C/T]TCTTAATTTTCATAA	207278
rs215912282	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101267581	TTTAGGAACCAGATG[A/T]CTTGCCCAGGGTCAC	207278
rs215948542	in-del	-/TTTA			intron-variant	Fchsd2	Mm_Celera	7:101172143	TTTTTTATTGGTTAT[-/TTTA]TTTATTTATTTATTT	207278
rs215970373	in-del	-/TTC			intron-variant	Fchsd2	GRCm38.p3	7:101173197	AAAAAAAAGAATAAA[-/TTC]AAAAGAGAGTGATTA	207278
rs216009647	in-del	-/ATTCACAAAGATTTGCCT			intron-variant	Fchsd2	Mm_Celera	7:101271357	GAAACTTTGTAGACC[-/ATTCACAAAGATTTGCCT]GCCTCTGCCTCCTGT	207278
rs216042533	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101212533	TAAATGAGGCGTTTT[A/G]CTCAGTTACAAGAAG	207278
rs216072312	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101159942	AAAAGATGGCCTAGT[C/T]GGCCATCAGTGGAAA	207278
rs216096270	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101141705	ATATATGTAGTCTTC[C/T]AGTCAGCTATCCTAA	207278
rs216125092	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101253785	TTTGTGTACCTGTAG[A/C]ACGTAACAACGAAAA	207278
rs216148788	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101155360	GTGCGGTGGTTCATA[C/T]GTGTACTCGCAGCCC	207278
rs216159479	in-del	-/ACACACACAC			intron-variant	Fchsd2	Mm_Celera	7:101172053	GTATAGCCTAAACCT[-/ACACACACAC]ACACACACACACACA	207278
rs216162699	snp	A/C/T			intron-variant	Fchsd2	Mm_Celera	7:101112050	CGCCAGGCTGGGATT[A/C/T]TTTTCTTTTTTTTTT	207278
rs216172237	in-del	-/G			intron-variant	Fchsd2	Mm_Celera	7:101196665	CTTATTGCAGGGGTT[-/G]GGGGTCTCCAGAGCC	207278
rs216200582	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101235721	CTTAATGGTCAATTC[A/G]GGTTTTCTGAAAATT	207278
rs216215176	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101202682	ATGAACTGTTGGAGT[A/G]CATGAAGGGCTGATT	207278
rs216255566	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101197427	AGAACCTACTTCCTG[C/T]GTGTTCTCCTCTAAC	207278
rs216273530	snp	C/G			upstream-variant-2KB	Fchsd2	GRCm38.p3	7:101108681	TCCTCCTCAGCCGCC[C/G]GGCGAGCCGCGAGCC	207278
rs216279672	in-del	-/TAGTG			intron-variant	Fchsd2	Mm_Celera	7:101261088	CCATAGCATCAGTAA[-/TAGTG]TCAGGCCTTAGAGCC	207278
rs216284251	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101213692	CATCTGTAACTCACA[A/G]AGGATCTGACACCTC	207278
rs216302139	in-del	-/TT			intron-variant	Fchsd2	Mm_Celera	7:101146989	TGATTGGCTAACAGC[-/TT]TTTTTTTTCTTACAG	207278
rs216313621	in-del	-/GGGGG			intron-variant	Fchsd2	Mm_Celera	7:101216190	ATGAAAAGACAAAAT[-/GGGGG]GGGGGGGGTCCAAAA	207278
rs216331629	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101111333	TTAATATCTGGGATG[A/C]GCCAGTCACCCCAGA	207278
rs216335387	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101184027	ACCTAATGAGGTAGA[A/G]CAAACCAAAGAGAGC	207278
rs216353170	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101223554	TCTTTATATATTTTG[A/G]ATATTAACCCTCTGT	207278
rs216369404	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101196019	GTCTGGAATATCTTA[A/T]GTTTTGTTTGTTTGT	207278
rs216380171	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101132634	ATAAATCAGTTGGTA[C/T]CATTTTTCTAGAGGC	207278
rs216427841	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101143308	AGAATTAGGATTACA[C/T]GTGTGTATGTATGTG	207278
rs216446953	in-del	-/C			intron-variant	Fchsd2	Mm_Celera	7:101120112	TCTTTTTCTTTCTTT[-/C]TTTTTTTTTTTTAAG	207278
rs216507652	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101131518	TTCAGTTCCGTCTCT[C/G]CTTCTTCAGAACACG	207278
rs216531691	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101256017	CTTGTTTATTATTCT[G/T]CTTTGTCTAGTCTCT	207278
rs216537791	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101144727	AAGGAAGTCTAGTGG[A/G]CTTCTGAATGCAGCT	207278
rs216570071	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101281239	GGAGGGAAGCAGAAC[A/C]GATGCAGGGAGCCAC	207278
rs216571193	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101185066	CTATAATTAAGCAGT[G/T]TTATACAAATACTTG	207278
rs216596886	in-del	-/AA			intron-variant	Fchsd2	Mm_Celera	7:101188228	TTGGATTCAGAAATT[-/AA]AAAAAAAAAAACCCT	207278
rs216598610	in-del	-/TTGTTTTGTTTTGTT			intron-variant	Fchsd2	Mm_Celera	7:101209786	TAGTAGAATAAAAAC[-/TTGTTTTGTTTTGTT]TTGTTTTGTTTTTCA	207278
rs216640913	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101197320	AGCAAGCTGGTGAGT[C/T]GTCTGTTGAGCTGGG	207278
rs216672066	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101255030	CACCAGTTCTGGGCT[C/T]GGGGTCTTTTCGCCT	207278
rs216689268	in-del	-/TT			intron-variant	Fchsd2	Mm_Celera	7:101111891	GTTGGGATTATTTTC[-/TT]TTTTTTTTTTTGTTT	207278
rs216695817	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101280351	GGTATTGAATTTTAT[A/C]AAAGGCTTTTTCAGC	207278
rs216704801	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101156292	AGCAAGATAGGTGAG[A/C]GGCACAGTGGTTTCA	207278
rs216772575	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101146297	GTCATCCTACCTTAG[A/G]ATATCATCTGCTGCT	207278
rs216773902	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101225098	CTGGATGGCCTGTCA[A/G]TTGGTGGGGTGGTAT	207278
rs216795130	in-del	-/AG			intron-variant	Fchsd2	Mm_Celera	7:101262395	TGTGGTGACACATTT[-/AG]AAGAGAGTTGTGGGG	207278
rs216807489	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101148470	AAGAAGGCATAAAGT[A/G]TCCTGGAACTGGAGT	207278
rs216823163	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101198618	CATGAAGGTAACGCC[A/C]TGAATATTTGTGGTA	207278
rs216850424	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101227235	CAGACACATGCTACA[A/G]ACATCATTACTAAAA	207278
rs216861698	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101239339	ACCTAAGACAGGTTC[C/T]TTGTGTTTTTAAATT	207278
rs216914630	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101123850	ATCCACTTGCAATGT[A/T]CAGTTACTGATTCTT	207278
rs216956559	in-del	-/A			intron-variant	Fchsd2	Mm_Celera	7:101111429	GATATGTCATGTTTT[-/A]ACTAAAGCTACCTAT	207278
rs216980015	snp	C/T			intron-variant	Fchsd2	GRCm38.p3	7:101134240	CCCCCAACCCCCCAA[C/T]ACACTCCTCCTCTAT	207278
rs217006688	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101226026	GGGGGGCATCCACAT[A/G]GAGATGGGTGGGGTG	207278
rs217021108	in-del	-/CA			utr-variant-5-prime, upstream-variant-2KB	Fchsd2	Mm_Celera	7:101108893	CCCAGGCTCTCCTTT[-/CA]CACACACACACAAGC	207278
rs217053928	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101135275	GGGAGGTCAGCTCTC[A/T]GGGCATTGTACATTC	207278
rs217058877	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101172566	AAGATGGAGAAACTG[A/G]AACAAGTAACTGTGG	207278
rs217059125	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101188229	TTGGATTCAGAAATT[A/T]AAAAAAAAAACCCTC	207278
rs217085187	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101270255	TTAAAGGTGTGGGCC[A/G]GGCCTAGCAAACACA	207278
rs217093519	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101281324	GAGTAAAGAGGACTC[A/G]TCTGTCCATACACAT	207278
rs217096857	snp	A/G			intron-variant, upstream-variant-2KB	Fchsd2	Mm_Celera	7:101109787	CTGGGTGGCAGTGAC[A/G]GTGCTCTGGGGCTGC	207278
rs217114358	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101174068	TACTGATAATGGTCA[G/T]GGAGTATTTCTGAGC	207278
rs217114663	snp	A/G			intron-variant	Fchsd2	GRCm38.p3	7:101137354	TATGTATGTATGTAT[A/G]TATGTATGTATGTGT	207278
rs217122636	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101185248	TCAATGTTGAGGAAA[A/G]ATATCTGTTATTTGA	207278
rs217181081	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101268872	GACTTTGACTGCTCT[C/T]CACGCTTCCTAGAAA	207278
rs217197526	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101187203	GAAAAAGTTTCATTA[A/G]TTAGTCTTAATTTCA	207278
rs217238680	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101226126	GTAAAAACTAAATTA[A/G]AAATAAAATAAAATT	207278
rs217246022	in-del	-/C			intron-variant	Fchsd2	Mm_Celera	7:101130601	AATGACTCACTGTAG[-/C]CCTGGCTAGCTTTGA	207278
rs217249500	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101162977	ATTTCTGTCTGTGTG[-/T]GTCCCCCCCCCCTTT	207278
rs217274333	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101227627	GTCTTCCAGGATTGC[A/C]GCACACTGGAGATGG	207278
rs217276184	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101135399	CCCAGGTGGCTAGGA[G/T]TATAGGTATGTACTA	207278
rs217277028	in-del	-/A			intron-variant	Fchsd2	Mm_Celera	7:101117801	TAAGTAAATCTTAAG[-/A]AAAAAAAAAGAAGAG	207278
rs217303443	in-del	-/AT			intron-variant	Fchsd2	Mm_Celera	7:101272488	CTTTTTTAAAAAAAA[-/AT]GTCTTTCCCTTAAAA	207278
rs217310940	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101200069	TGGGAAAGAGATCAA[C/T]TTTGTCCATAAACAA	207278
rs217320934	in-del	-/CACACG			intron-variant	Fchsd2	Mm_Celera	7:101163399	ACACACACACACACA[-/CACACG]AAACACTAAAGAAAA	207278
rs217322709	in-del	-/GGGTAG			intron-variant	Fchsd2	Mm_Celera	7:101217376	ACGCCTACTCAGCCT[-/GGGTAG]ACTTATACTTAAATC	207278
rs217330788	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101228636	GAAACACAGCTGCTT[A/T]AAGACATTCAAATTC	207278
rs217362347	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101127796	ACCTGAGGATAGATA[C/T]AAAATCTGAGAACTA	207278
rs217369202	in-del	-/TCC			intron-variant	Fchsd2	Mm_Celera	7:101251044	AACCTGCATCCTCTG[-/TCC]TCCTTCTTCCTGCCA	207278
rs217383519	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101152672	AGCACATTTCTGGTA[-/T]TTTTTAATGTATTCA	207278
rs217399629	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101241295	GAGGTCCCATTTGTT[A/G]AGCCTTGATCTTACA	207278
rs217410079	snp	C/G			intron-variant	Fchsd2	GRCm38.p3	7:101147457	AGATAGAGACAGAAA[C/G]TGGAGAGAGGAGTGA	207278
rs217415236	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101137205	TCCTACTTAGAAAAT[G/T]TATTGACAGGTTTTC	207278
rs217457056	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101216758	TTTTAGATACAATTT[A/T]ATTTTTAAGGTAGAA	207278
rs217472008	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101127278	GATGTGGTTGCCATG[G/T]ACAGTCAGTTTACTT	207278
rs217477555	snp	G/T			intron-variant	Fchsd2	GRCm38.p3	7:101177705	ATATACACACACACA[G/T]ATGTATATACATACA	207278
rs217522689	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101178575	ACAGTAAAAAGTTCA[A/G]GATGGCTAGTGTGAA	207278
rs217524334	in-del	-/AA			intron-variant	Fchsd2	Mm_Celera	7:101268486	ACTATCACACCCTCC[-/AA]AAAAAAAAAAAATGT	207278
rs217593511	snp	C/G			intron-variant	Fchsd2	Mm_Celera	7:101215462	AAGTTATCCAAGGAT[C/G]AAGGTACCAGGACAG	207278
rs217605560	in-del	-/A			intron-variant	Fchsd2	Mm_Celera	7:101126082	TTATCATAATAGGCT[-/A]AAAAAATCATTGGAC	207278
rs217700573	in-del	-/AG			intron-variant	Fchsd2	Mm_Celera	7:101259912	AGCTTAGTACAGCAA[-/AG]AGAAGAGGGAGGAGA	207278
rs217725859	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	Fchsd2	Mm_Celera	7:101108878	CCTCTTCCTTCTCCT[C/T]CCCAGGCTCTCCTTT	207278
rs217745622	in-del	-/CTTA			intron-variant	Fchsd2	Mm_Celera	7:101112954	CAGGTCCAACCAATT[-/CTTA]CTTATATAATAGTTA	207278
rs217804276	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101273505	CAAATCCCCAACCCT[A/G]GGACCAGTGCTTGAT	207278
rs217820774	in-del	-/T			intron-variant	Fchsd2	Mm_Celera	7:101277370	CAAAAGCAGTGCGCC[-/T]TGCCTGTCTCTTACC	207278
rs217821763	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101146642	TCATAGAGCCTGAGC[A/G]CTGGGATTAAAGGTG	207278
rs217862442	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101170001	AACAGTAATACAAGC[A/C]ATAAACTTTAGCTAA	207278
rs217919476	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101145701	AAATTAAATTAAAAA[A/T]ATATTTTTCTAAGGT	207278
rs217934526	snp	A/G			upstream-variant-2KB	Fchsd2	Mm_Celera	7:101107141	TCCTGGTCTAGTCCA[A/G]TCTCATGGACTTCCT	207278
rs217944195	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101158867	ATAAGTATTTAAATA[A/C]AATCCTTCTTTAAAT	207278
rs217997127	snp	A/C			intron-variant	Fchsd2	Mm_Celera	7:101200292	GAGAGCAGCCTGATG[A/C]GAGTTCTGCTTACCC	207278
rs218051424	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101187498	TATTGTGATACATAC[C/T]TACTATTCAGGAGGC	207278
rs218094616	snp	A/T			intron-variant	Fchsd2	Mm_Celera	7:101256101	TTGTAATTAATGAAA[A/T]AACTTTTACAGTGAG	207278
rs218103035	in-del	-/TG			intron-variant	Fchsd2	Mm_Celera	7:101201347	GTTTGAAGCCATCTT[-/TG]TGTATATATAGTGAG	207278
rs218124723	snp	A/G			upstream-variant-2KB	Fchsd2	Mm_Celera	7:101108428	GGTGTGGCCGGGAGC[A/G]CATCCCCTCTGCAGC	207278
rs218148771	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101239483	TGAGTTAGGGGCCAG[A/G]CTAGGCTACATGAGG	207278
rs218220075	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101255258	AGAGTTGTACTTGTT[G/T]CTTTTACACTATGAT	207278
rs218233761	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101111509	TTGTGAGAATGAATG[C/T]TATAACAGGGTAGTA	207278
rs218246816	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101156991	TGCTCCAAAGATCCA[C/T]GAAAGTACTAAAACA	207278
rs218269508	in-del	-/ATAT			intron-variant	Fchsd2	Mm_Celera	7:101192324	ATATTTATTATACAC[-/ATAT]ATATATGTATATACA	207278
rs218280886	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101188543	GAAGGGGGACTGGAA[A/G]GCAGAAGAAGAGAAT	207278
rs218281269	snp	G/T			intron-variant	Fchsd2	Mm_Celera	7:101267397	CATCTGACTCTCTGT[G/T]CCTCATAAAACCAGC	207278
rs218309534	in-del	-/TCCA			intron-variant	Fchsd2	GRCm38.p3	7:101138252	GTGCCTGTCAGTCTT[-/TCCA]TCCATCCATCCATCC	207278
rs218312904	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101257968	TGGTTTTTCTTGTTT[C/T]TCTGCTTTAGTGGTT	207278
rs218336309	snp	C/T			intron-variant, upstream-variant-2KB	Fchsd2	Mm_Celera	7:101110437	CTGTGCTCCCTGCTC[C/T]TGTGGTTAATGTCTG	207278
rs218341724	snp	C/T			intron-variant	Fchsd2	Mm_Celera	7:101255963	ATCATACCCTTTGTA[C/T]TTCCTTTGTATTTCC	207278
rs218359245	snp	A/G			intron-variant	Fchsd2	Mm_Celera	7:101228864	CACAACCATCTGTAT[A/G]TAATTTTAGTCTCAG	207278

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