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

LRSAM1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1317843	snp	C/T	0.341235	0.232758	intron-variant	LRSAM1	GRCh38.p7	9:127490007	AAAGTGACCTCGGCC[C/T]AGGAGGAGGCGGTCC	90678
rs1317844	snp	C/T	0.183886	0.241099	intron-variant	LRSAM1	GRCh38.p7	9:127490033	GGTCCTCCTCTTAGA[C/T]CCTCCCTCATGTGAC	90678
rs1539564	snp	C/T	0.45866	0.137698	intron-variant	LRSAM1	GRCh38.p7	9:127491652	GCCCTGGAGGATGTG[C/T]GCCTGGGGGCCTAAA	90678
rs1539567	snp	C/T	0.345853	0.230894	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479887	GCTGCCGCTCTGCGT[C/T]GAGGTGGCGCTGGTG	90678
rs1539568	snp	A/G	0.488218	0.0758443	intron-variant	LRSAM1	GRCh38.p7	9:127479830	ACTGCTCCTGCAGCC[A/G]GAGGTAGGGGTCCTG	90678
rs1539569	snp	A/G	0.345065	0.23122	intron-variant	LRSAM1	GRCh38.p7	9:127479543	GCCACTGGCTGGGGG[A/G]TGCAGCCAGGCTGGA	90678
rs1547840	snp	A/T	0.471673	0.115589	intron-variant	LRSAM1	GRCh38.p7	9:127490028	ATGAGGGAGGGTCTA[A/T]GAGGAGGACCGCCTC	90678
rs1547841	snp	C/G	0.394538	0.203982	intron-variant	LRSAM1	GRCh38.p7	9:127489971	AGGCGTCAGGACCAC[C/G]GTGGCTCACAGCTCC	90678
rs2243464	snp	A/T	0.458545	0.137872	intron-variant	LRSAM1	GRCh38.p7	9:127486087	TGTGGTTCATCGCTT[A/T]GCCGAGTGCCTGCCA	90678
rs2243509	snp	C/G	0.432944	0.170387	intron-variant	LRSAM1	GRCh38.p7	9:127454771	CTGCCAAGGGTGCTT[C/G]TCCCCTGTAGACTGA	90678
rs2243608	snp	C/T	0.493013	0.058691	intron-variant	LRSAM1	GRCh38.p7	9:127464630	TCTCGACATCTAGTA[C/T]GAGTTCTGGACACTT	90678
rs2243663	snp	A/G	0.493837	0.055168	intron-variant	LRSAM1	GRCh38.p7	9:127460173	cctggctaatttttt[A/G]tattttagtagagac	90678
rs2243767	snp	C/T	0.484801	0.0858387	intron-variant	LRSAM1	GRCh38.p7	9:127459109	CCACCTCGGATGGCC[C/T]TAGTGAGACCAGGCA	90678
rs2243784	snp	A/G	0.49306	0.0584955	intron-variant	LRSAM1	GRCh38.p7	9:127458677	CTGTGGAGTACCACT[A/G]TCAATATTTTATCGC	90678
rs2243898	snp	C/G	0.492188	0.0620098	intron-variant	LRSAM1	GRCh38.p7	9:127457711	GAAGAGGAGGGACGC[C/G]CAGGTGATCTGGAAG	90678
rs2243903	snp	C/T	0.49263	0.0602539	intron-variant	LRSAM1	GRCh38.p7	9:127457464	CTGAGCGCCTGCTCC[C/T]TTTGGGCTGCCTCTT	90678
rs2243906	snp	C/T	0.484948	0.0854709	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457390	GAGTCTGGCAACCAT[C/T]AAGGTACTGGGCCCT	90678
rs2244218	snp	G/T	0.449345	0.150869	intron-variant	LRSAM1	GRCh38.p7	9:127454672	GTAGGCCTCCGCACT[G/T]CCCCCAACAAGCCGT	90678
rs2244331	snp	G/T	0.455621	0.142197	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453841	AAGAACTAGAAAGAC[G/T]CAGCCCCTCACCTCA	90678
rs2244468	snp	A/G	0.493703	0.0557558	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453000	GGTCAGGACTTGAGA[A/G]ACCACGGTTCCAGGC	90678
rs2244624	snp	A/G	0.492533	0.0606443	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451229	CTTTGCACGCGCGGC[A/G]GGGCCGAGGGATGCT	90678
rs2245461	snp	A/G	0.44858	0.151875	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503809	GCAGCTGAGGCTGAT[A/G]GGGGTAAATGCTCAG	90678
rs2245645	snp	A/G	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127502151	CCTCCGGCAGGGGCC[A/G]GCGGAATAGGCCTCC	90678
rs2245677	snp	A/G	0.455024	0.143057	intron-variant	LRSAM1	GRCh38.p7	9:127489233	GGAAACTCAGGGTGC[A/G]ATGCCGGAAGTGCAT	90678
rs2246000	snp	A/G	0.487432	0.0782705	intron-variant	LRSAM1	GRCh38.p7	9:127486865	TTCATAATAGCAACT[A/G]TTTTTTCCCAGTGAG	90678
rs2246011	snp	C/T	0.499902	0.00698814	intron-variant	LRSAM1	GRCh38.p7	9:127486606	CCCCCTTTCCTGATA[C/T]GTGACACTGTGCTTA	90678
rs2246267	snp	C/T	0.395087	0.203592	intron-variant	LRSAM1	GRCh38.p7	9:127484381	TGCCACATTTTCTTT[C/T]TTTCTTTTTTCCTTG	90678
rs2246270	snp	C/T	0.394904	0.203722	intron-variant	LRSAM1	GRCh38.p7	9:127484285	TTTTTTTTTTTCCTG[C/T]TTCTTTATTTCTAAA	90678
rs2246375	snp	G/T	0.456095	0.141508	intron-variant	LRSAM1	GRCh38.p7	9:127483508	TTTAAATAAATGTTG[G/T]TGATCCATATGCTGT	90678
rs2246579	snp	A/T	0.486725	0.0803809	intron-variant	LRSAM1	GRCh38.p7	9:127481976	CAGAAAAAAAATCTA[A/T]ATTTCTGGAAAGAAA	90678
rs2246600	snp	A/G	0.458084	0.138567	intron-variant	LRSAM1	GRCh38.p7	9:127481567	AGAGCAGCTTTGAGG[A/G]GAGAATGTCTTGTGA	90678
rs2247303	snp	A/G	0.492679	0.0600586	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451019	CGCTAACCCAGGCCA[A/G]TGGGGCGAAACGCCC	90678
rs2247310	snp	C/G	0.493599	0.0562105	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450831	GAAGAGTTAGTGTCT[C/G]TGCAGAGGGAGCCCC	90678
rs2247322	snp	A/T	0.493523	0.0565391	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450597	AAGGTACCTAGTACT[A/T]GTTCAGTGGCTCAGG	90678
rs2248725	snp	C/T	0.454904	0.143228	intron-variant	LRSAM1	GRCh38.p7	9:127498509	CAGCAGTCCTCAGGA[C/T]CGGCTGCTTCTCACT	90678
rs2248822	snp	A/C	0.349407	0.229396	intron-variant	LRSAM1	GRCh38.p7	9:127497339	GATCCAGCCAGGTAC[A/C]AGCACAGCTCCAGCC	90678
rs2249052	snp	A/T	0.458084	0.138567	intron-variant	LRSAM1	GRCh38.p7	9:127495881	ATGTATTATGTTATA[A/T]ATATTCAAACCCTTC	90678
rs2249282	snp	C/G	0.394904	0.203722	intron-variant	LRSAM1	GRCh38.p7	9:127493531	CTTTCTCAAGGCTGT[C/G]CGTGGCCCCTATTGT	90678
rs2249290	snp	C/T	0.451109	0.148509	intron-variant	LRSAM1	GRCh38.p7	9:127493289	CTGGTCTCCAACTCC[C/T]GGGCTCAAACGATCT	90678
rs2249649	snp	A/G	0.396364	0.202676	intron-variant	LRSAM1	GRCh38.p7	9:127478701	AAGAGCCCCTCCTAC[A/G]GTGCCATGCACACAG	90678
rs2249791	snp	A/G	0.398174	0.201356	intron-variant	LRSAM1	GRCh38.p7	9:127478040	ctgggcaacaagagc[A/G]aaactccgtctcaaa	90678
rs2249803	snp	A/G	0.456095	0.141508	intron-variant	LRSAM1	GRCh38.p7	9:127477621	caggcatggtggtgc[A/G]tgcctgcagtctcag	90678
rs2249936	snp	C/G	0.449853	0.150196	intron-variant	LRSAM1	GRCh38.p7	9:127476366	GCCTGGGCAATGTGG[C/G]GAGACCCTGTCTCTA	90678
rs2249940	snp	A/G	0.487241	0.0788465	intron-variant	LRSAM1	GRCh38.p7	9:127476261	TCGGCTCGCTGGGAC[A/G]CATGGATTAGTGAAA	90678
rs2250020	snp	C/T	0.457853	0.138915	intron-variant	LRSAM1	GRCh38.p7	9:127475881	gagtagctgggatta[C/T]agggatgcgccacca	90678
rs2250021	snp	C/T	0.457853	0.138915	intron-variant	LRSAM1	GRCh38.p7	9:127475843	tctcccgggttcaag[C/T]gattctcctgcctca	90678
rs2250024	snp	A/T	0.487177	0.0790385	intron-variant	LRSAM1	GRCh38.p7	9:127475745	aagattttattattt[A/T]tttatttttttttga	90678
rs2250161	snp	C/T	0.456622	0.140738	intron-variant	LRSAM1	GRCh38.p7	9:127475077	ATTATTATTATTTTA[C/T]AGTTCAGCAAGAATT	90678
rs2250184	snp	C/G	0.4582	0.138394	intron-variant	LRSAM1	GRCh38.p7	9:127474310	TCTTGCTCCATCACC[C/G]AGGCTGGAGTGCAGT	90678
rs2250267	snp	A/G	0.487889	0.0768691	intron-variant	LRSAM1	GRCh38.p7	9:127473964	GCTGCACGCATACAT[A/G]TGTGTGTGTGCGTGT	90678
rs2250271	snp	A/G	0.00475057	0.0485048	intron-variant	LRSAM1	GRCh38.p7	9:127473739	TGGCAGTGGGAGCGG[A/G]TGTCTCTGGGTACCT	90678
rs2253411	snp	C/G	0.431621	0.171796	intron-variant	LRSAM1	GRCh38.p7	9:127470630	TGTCCATTAGGAGTA[C/G]AATGGATAACTAAAC	90678
rs2253414	snp	A/T	0.431473	0.171952	intron-variant	LRSAM1	GRCh38.p7	9:127470611	aacctggaaacagct[A/T]taatgtccattagga	90678
rs2253639	snp	A/G	0.492484	0.0608394	intron-variant	LRSAM1	GRCh38.p7	9:127469138	ATCCTACAGATCCAC[A/G]AGGAAAAGACATTAG	90678
rs2253669	snp	A/G	0.490398	0.0686206	intron-variant	LRSAM1	GRCh38.p7	9:127468235	GAGAAGAGAGATGGG[A/G]GAAGCCAAAGACAGT	90678
rs2253806	snp	A/G	0.491834	0.0633738	intron-variant	LRSAM1	GRCh38.p7	9:127467373	ctgctggtgcagctc[A/G]cctcaatatcttatc	90678
rs2253811	snp	A/C	0.456685	0.140646	intron-variant	LRSAM1	GRCh38.p7	9:127467285	aaacagttccaggtg[A/C]aggggcttaaactat	90678
rs2253898	snp	A/G	0.465788	0.126237	intron-variant	LRSAM1	GRCh38.p7	9:127466983	GTCTGGGCAATGGGA[A/G]TGAGACCCTGTCTCA	90678
rs2253928	snp	C/G	0.493013	0.058691	intron-variant	LRSAM1	GRCh38.p7	9:127466290	CTCCAGCCTGCCACA[C/G]AGCAAGACTCTGTCT	90678
rs2253929	snp	C/T	0.492918	0.0590819	intron-variant	LRSAM1	GRCh38.p7	9:127466232	GAGAATTGCTTGAAC[C/T]GGGGAGGCAAAGGTT	90678
rs2253930	snp	A/G	0.4661	0.125701	intron-variant	LRSAM1	GRCh38.p7	9:127466216	CGGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC	90678
rs2254041	snp	C/T	0.492966	0.0588865	intron-variant	LRSAM1	GRCh38.p7	9:127466165	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCGCA	90678
rs2254164	snp	A/T	0.465892	0.126058	intron-variant	LRSAM1	GRCh38.p7	9:127464800	GGTGTACCCCATCAC[A/T]CTTGGCTAATTTTTT	90678
rs2254437	snp	A/G	0.49306	0.0584955	intron-variant	LRSAM1	GRCh38.p7	9:127462648	AAGAAAGTTGTCGGT[A/G]GGGGAACAACACAGT	90678
rs2254541	snp	A/G	0.332106	0.236133	intron-variant	LRSAM1	GRCh38.p7	9:127461475	CTGAGAGCCAGGGCC[A/G]TATGGCCGTATGGGG	90678
rs2255483	snp	A/G	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127460339	GTGTGTCATCCTGCT[A/G]GCCTTGCTCACCTCG	90678
rs2265685	snp	C/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127458382	cgacagagcgagact[C/T]cgtctcaaaaacaaa	90678
rs2265687	snp	A/G	0.030665	0.119967	intron-variant	LRSAM1	GRCh38.p7	9:127469435	agattgtgccactgc[A/G]ctccagtctggatga	90678
rs2265688	snp	A/G	0.488241	0.0757703	intron-variant	LRSAM1	GRCh38.p7	9:127500318	GTGAGCCGAGATCGC[A/G]CCACTGAACTCCAGC	90678
rs2488899	snp	A/T	0.493837	0.055168	intron-variant	LRSAM1	GRCh38.p7	9:127459419	agatggtgtttcgcc[A/T]tgttggcctgactgg	90678
rs2488900	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127466494	tatatatatatatat[A/T]ttttttttttttttt	90678
rs2488901	snp	C/T	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127466531	TTTTTTTTTTTTTTT[C/T]CACTAGAGATGGGGT	90678
rs2488902	snp	C/T	0.432357	0.171014	intron-variant	LRSAM1	GRCh38.p7	9:127498806	gctcacacctgtaat[C/T]ccagcactttgggag	90678
rs2488903	snp	A/G	0.489665	0.0711382	intron-variant	LRSAM1	GRCh38.p7	9:127499797	cagtggcgtgtgcct[A/G]tagtcccagatacgc	90678
rs2491101	snp	C/T	0.455502	0.142369	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452970	TGAGCACCAAGCAGT[C/T]GGGCAAATCCCATAG	90678
rs2798428	snp	C/T	0.487305	0.0786545	intron-variant	LRSAM1	GRCh38.p7	9:127494926	ATGATGGTTATGAAC[C/T]ATGCTCCTCTGAGCG	90678
rs2798429	snp	C/T	0.455144	0.142885	intron-variant	LRSAM1	GRCh38.p7	9:127494912	CCATGCTCCTCTGAG[C/T]GGGTGGACAGCACTT	90678
rs2798430	snp	A/T	0.449091	0.151204	intron-variant	LRSAM1	GRCh38.p7	9:127458600	TTTTTAATTTAATTT[A/T]ATTTTATTTTGTTTT	90678
rs2806714	snp	A/C	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127468834	aaaaaaaaaaaaaaa[A/C]aaaaatcagccaggc	90678
rs2995822	snp	A/G	0.455858	0.141853	intron-variant	LRSAM1	GRCh38.p7	9:127472355	CTTTTAAAAAACATT[A/G]AAGAGGCTGGGCATG	90678
rs2995823	snp	A/G	0.486984	0.079614	intron-variant	LRSAM1	GRCh38.p7	9:127472368	TTAAAGAGGCTGGGC[A/G]TGGTGACTCACACCT	90678
rs3053015	in-del	-/TC	0.375	0.216506	intron-variant	LRSAM1	GRCh38.p7	9:127489560	GCCACTCTGCAAGTC[-/TC]TGAGAGAGCAGGTCC	90678
rs3053020	in-del	-/GT/TG			intron-variant	LRSAM1	GRCh38.p7	9:127479096	AGGATGCAGCAGACT[-/GT/TG]GCGTGTAAGAGGAAG	90678
rs3802358	snp	C/T	0.248416	0.249995	intron-variant	LRSAM1	GRCh38.p7	9:127497377	CAGAGCCCACACATA[C/T]GGCTGGAGCCCTGCC	90678
rs3802360	snp	C/T	0.00163535	0.0285482	intron-variant	LRSAM1	GRCh38.p7	9:127497215	AGACTGTGGCCTGGG[C/T]GGGAGCCCGCTAAAT	90678
rs3802361	snp	A/G	0.00954246	0.0684118	intron-variant	LRSAM1	GRCh38.p7	9:127496131	GGACAGCGGCCTTGC[A/G]TGCCCCTCCCCTCCA	90678
rs3808831	snp	A/G	0.242488	0.249887	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452135	GTCCAGCCTAGATGC[A/G]GGGGGAGGGCCACAC	90678
rs3808832	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451550	CAGCGCACCGCGGTG[C/T]CCTGCTTGCCAGCCG	90678
rs3808833	snp	A/C/T	0.0205649	0.0992992	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451369	GAGGCCAAGGTGCAA[A/C/T]TTCCTTCGGTCGTCC	90678
rs3808834	snp	C/T	0.000308732	0.0124206	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451322	CGACACCAGCCGCCT[C/T]CACCATGCCGCCGAA	90678
rs3840733	in-del	-/C	0.247265	0.249985	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452325	AAACAGCCCTCCCCC[-/C]ATCCGTCCCTGATGA	90678
rs3935304	snp	A/G	0.318174	0.240525	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503966	CAGAGGTGCACGTTG[A/G]TTATGCATTTTCCGG	90678
rs4836563	snp	A/G	0.257176	0.249897	intron-variant	LRSAM1	GRCh38.p7	9:127492401	TTTCCAAGAGCAGGC[A/G]CAGGAGTGAAGCAGG	90678
rs4836564	snp	A/G	0.284471	0.247612	intron-variant	LRSAM1	GRCh38.p7	9:127493227	CCACCATGCCTGGCA[A/G]ATTTTTTTATTTTTT	90678
rs4837153	snp	C/T	0.316	0.241131	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451143	CAGAAAGGCTGAGGC[C/T]TGGCCGGGGCGGCGC	90678
rs4837154	snp	G/T	0.245346	0.249957	intron-variant	LRSAM1	GRCh38.p7	9:127457130	CCCTTGAAGATCCAG[G/T]TTTTAAGGAAGGGCA	90678
rs4837155	snp	C/T	0.0433465	0.140692	intron-variant	LRSAM1	GRCh38.p7	9:127469593	ATACTTTGACAAACC[C/T]ACTAAAATGGCCAGA	90678
rs5900748	in-del	-/A	0.394538	0.203982	intron-variant	LRSAM1	GRCh38.p7	9:127491007	ACAAGCACGTCCATG[-/A]CCCCAGGAACGCGAG	90678
rs7019372	snp	C/T	0.0128825	0.0792169	intron-variant	LRSAM1	GRCh38.p7	9:127501175	CCCCACCCGCCTGCC[C/T]TGCCTGTGGCCACCC	90678
rs7023786	snp	A/G	0.0501905	0.150254	intron-variant	LRSAM1	GRCh38.p7	9:127477906	tacagaaaatcagcc[A/G]ggtgtggtggtgggt	90678
rs7034813	snp	G/T	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127483512	AATAAATGTTGGTGA[G/T]CCATATGCTGTGGCA	90678
rs7045257	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127466506	tatatatatatatat[A/T]tTTTTTTTTtttttt	90678
rs7469828	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127469844	gtggcgggcgcctgt[A/G]gtcccagctactagg	90678
rs7849608	snp	A/G	0.326506	0.238006	intron-variant	LRSAM1	GRCh38.p7	9:127459253	gcagtgcctcactgc[A/G]ttgcccaggctgggg	90678
rs7851331	snp	A/C	0.0322973	0.122905	intron-variant	LRSAM1	GRCh38.p7	9:127454968	AGGTGTTTTGTCTTA[A/C]TACTTTTTAAAAATT	90678
rs7856679	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127466504	tatatatatatatat[A/T]tTTTTTTTTTTtttt	90678
rs7856923	snp	A/T	0.317451	0.240729	intron-variant	LRSAM1	GRCh38.p7	9:127496818	GCACTGAGGGTCACA[A/T]GGCCATGCCGCTCAG	90678
rs7858206	snp	A/G	0.244776	0.249945	intron-variant	LRSAM1	GRCh38.p7	9:127461543	TTTATAATGGTGAGT[A/G]TAGAGGACTGATGGG	90678
rs7859116	snp	C/T	0.0865458	0.189163	intron-variant	LRSAM1	GRCh38.p7	9:127470144	ggcccatgagttcca[C/T]tcctaggtacatgcc	90678
rs7868906	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127499537	ccctgtctaaaaaaa[A/T]atatatatatatata	90678
rs7874640	snp	A/C	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127458417	aacaaaacaaaacaa[A/C]acaaaaaaaaacaCC	90678
rs7874732	snp	A/C	0.493247	0.0577133	intron-variant	LRSAM1	GRCh38.p7	9:127458394	acttcgtctcaaaaa[A/C]aaaacaaaacaaaac	90678
rs7874738	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127458404	aaaaacaaaacaaaa[A/C]aaaacaaaacaaaac	90678
rs7874743	snp	A/C	0.498547	0.0269177	intron-variant	LRSAM1	GRCh38.p7	9:127458419	caaaacaaaacaaaa[A/C]aaaaaaaaacaCCag	90678
rs7874857	snp	A/G	0.0923359	0.194016	intron-variant	LRSAM1	GRCh38.p7	9:127458359	tgcagtccgcagtcc[A/G]gcgtgggcgacagag	90678
rs7875862	snp	C/G	0.458084	0.138567	intron-variant	LRSAM1	GRCh38.p7	9:127483266	cccaacttttccaag[C/G]ctcggttttcttagc	90678
rs9644915	snp	A/G	0.256619	0.249912	intron-variant	LRSAM1	GRCh38.p7	9:127477063	GTTCACTAACATTGG[A/G]TGAATTAGAGTAAAT	90678
rs9722268	snp	C/G	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127474945	GGGCAGGAGTACCAG[C/G]TGCCGGGCATTTGGC	90678
rs10607015	in-del	-/TA			intron-variant	LRSAM1	GRCh38.p7	9:127472298	TAAACTATGTAGAAG[-/TA]TATATATATATATAT	90678
rs10625871	in-del	-/CT	0.48995	0.0701706	intron-variant	LRSAM1	GRCh38.p7	9:127500351	GGTGACAGAGCGAGA[-/CT]CTGTCTCAAAAAAAA	90678
rs10760487	snp	A/G	0.259951	0.249802	intron-variant	LRSAM1	GRCh38.p7	9:127470459	GAGTTCCCGCCCCCA[A/G]CACGTGGGGATTACA	90678
rs10760488	snp	C/T	0.257176	0.249897	intron-variant	LRSAM1	GRCh38.p7	9:127473173	TTCTTGTGACGTGAC[C/T]GTATCCTTCCCATGA	90678
rs10819295	snp	A/G	0.341235	0.232758	intron-variant	LRSAM1	GRCh38.p7	9:127472774	CCTGTCTCATAGTAC[A/G]GTTTGAATGTCCCCT	90678
rs10819296	snp	A/G	0.257176	0.249897	intron-variant	LRSAM1	GRCh38.p7	9:127473618	ACTGACATTTACTGA[A/G]CACCTGCCACATTCC	90678
rs10819297	snp	C/T	0.256897	0.249905	intron-variant	LRSAM1	GRCh38.p7	9:127481341	CAGTGCAACCCCCGC[C/T]GCCCAGGTCCAAGCA	90678
rs10819298	snp	C/G	0.465052	0.127485	intron-variant	LRSAM1	GRCh38.p7	9:127494746	gtcaggagtttgaga[C/G]cagcctggccaacgt	90678
rs10987655	snp	G/T	0.326506	0.238006	intron-variant	LRSAM1	GRCh38.p7	9:127456093	GTGAATGATTTTTCA[G/T]CAGAGCATTGCAGCT	90678
rs10987656	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127456792	AATTGCTTGAACCTG[A/G]GAGGCGGAGGTTGCA	90678
rs10987657	snp	A/G	0.293037	0.246268	intron-variant	LRSAM1	GRCh38.p7	9:127464384	gctgtccagagcggc[A/G]gccactggccacgtg	90678
rs10987658	snp	C/T	0.281841	0.247964	intron-variant	LRSAM1	GRCh38.p7	9:127464396	ggcggccactggcca[C/T]gtgtatctattgagc	90678
rs10987659	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127466999	TGAGACCCTGTCTCA[A/G]AAAAATGTAAAAAAG	90678
rs10987660	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127471471	GAGAGACCTTATGTT[A/T]TAAAAAAAAAAAAAA	90678
rs10987661	snp	A/G	0.248471	0.249995	intron-variant	LRSAM1	GRCh38.p7	9:127475912	TGCCCGGCTAATTTT[A/G]TATTTTTAGTAGAGA	90678
rs10987662	snp	A/G	0.340784	0.232934	intron-variant	LRSAM1	GRCh38.p7	9:127476425	tagtggcacgtgcct[A/G]tggtcccagctacga	90678
rs10987663	snp	C/T	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127479246	TCTTACAGTTGGGCC[C/T]TGGAGGGGAGTGGGG	90678
rs10987664	snp	C/T	0.347473	0.230215	intron-variant	LRSAM1	GRCh38.p7	9:127484222	ttagcataatgtcct[C/T]gggttcatccatgtt	90678
rs10987665	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127484809	TGATTTTTCTTTTTT[C/T]CTTTTTTTTTTTTTT	90678
rs10987666	snp	C/T	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127484810	GATTTTTCTTTTTTT[C/T]TTTTTTTTTTTTTTT	90678
rs10987667	snp	G/T	0.281841	0.247964	intron-variant	LRSAM1	GRCh38.p7	9:127488758	CATGCCCAGCTAATT[G/T]TTTTTTATTTTTTGT	90678
rs10987668	snp	A/C	0.341235	0.232758	intron-variant	LRSAM1	GRCh38.p7	9:127489336	CTCTCTCAGAAAAAA[A/C]CCATCCATTAAGGTG	90678
rs10987669	snp	C/T	0.257732	0.24988	intron-variant	LRSAM1	GRCh38.p7	9:127491511	GTGGTCAGCCTGTTG[C/T]GAGGCAGGAGGGTCA	90678
rs10987670	snp	C/T	0.256619	0.249912	intron-variant	LRSAM1	GRCh38.p7	9:127499524	TGACAGAGCAAGACC[C/T]TGTCTAAAAAAAAAT	90678
rs10987671	snp	C/T	0.240171	0.249807	intron-variant	LRSAM1	GRCh38.p7	9:127502735	GGGACTCCTGGAACC[C/T]GGTAGGGCCAGCCAC	90678
rs11306296	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127499541	GTCTAAAAAAAAATA[-/T]ATATATATATATATA	90678
rs11462415	in-del	-/A	0.493881	0.054972	intron-variant	LRSAM1	GRCh38.p7	9:127469620	ATGGAAAAAAAAAAA[-/A]CAAAAAACTTCCTGC	90678
rs11542431	snp	C/T	1.72392e-05	0.00293586	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451337	GAATCCGGGTTCATC[C/T]GACACCAGCCGCCTC	90678
rs11789581	snp	C/T	0.251014	0.249998	intron-variant	LRSAM1	GRCh38.p7	9:127471019	ATTTTGTGCTCTTTT[C/T]TGTATGTATGTTATA	90678
rs11790775	snp	A/T	0.282369	0.247896	intron-variant	LRSAM1	GRCh38.p7	9:127464406	GGCCACGTGTATCTA[A/T]TGAGCACCTGGAGAc	90678
rs11791764	snp	A/G	0.084728	0.187577	intron-variant	LRSAM1	GRCh38.p7	9:127457932	gaataatgacaagag[A/G]aaagcctgtatgtgt	90678
rs11792666	snp	A/T	0.282369	0.247896	intron-variant	LRSAM1	GRCh38.p7	9:127464418	ctattgagcacctgG[A/T]GAccgtgctgtccag	90678
rs12001454	snp	A/G	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127500302	ggaggcagaggttgc[A/G]gtgagccgagatcgc	90678
rs12003794	snp	A/C	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127464594	aatacagCTCAGAGC[A/C]CGTTCCCAATCCTGA	90678
rs12338153	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127464397	gcggccactggccac[A/G]tgtatctattgagca	90678
rs12338502	snp	A/C	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127487219	CCAAGATGGTGCCAA[A/C]GCACAAACATACGTG	90678
rs12340522	snp	G/T	0.248755	0.249997	intron-variant	LRSAM1	GRCh38.p7	9:127471714	atcgcttgaacccat[G/T]aggcagaggctgcag	90678
rs12340560	snp	C/G	0.490007	0.0699769	intron-variant	LRSAM1	GRCh38.p7	9:127471875	gccatgttgaccagg[C/G]tggtctcatactctt	90678
rs12342959	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127464407	GCCACGTGTATCTAT[G/T]GAGCACCTGGAGAcc	90678
rs12345471	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127475341	actgaaaatgcaaaa[C/T]ttagccaggcatgga	90678
rs12345490	snp	G/T	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127475219	CTTTCCAATCAGTAA[G/T]AAGAAAACCATCGCA	90678
rs12347197	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127464388	tccagagcggcggcc[A/G]ctggccacgtgtatc	90678
rs12350191	snp	C/T	0.307176	0.243374	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454070	ACGCAGCCCCTGCCC[C/T]CGTGGAACTCACTAG	90678
rs12350192	snp	C/T	0.307176	0.243374	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454071	CGCAGCCCCTGCCCC[C/T]GTGGAACTCACTAGA	90678
rs12352893	snp	C/G	0.245061	0.249951	intron-variant	LRSAM1	GRCh38.p7	9:127456448	gttggccaggctggt[C/G]tcgaactcctgacct	90678
rs12377108	snp	A/G	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127466730	TCCAAAGTGAACTGA[A/G]Aggctgggtgtatga	90678
rs12553566	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127485099	aggcataagccacca[C/T]gcctggccTATTTTA	90678
rs12553626	snp	A/G			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450611	TTGTTCAGTGGCTCA[A/G]GCCTACTGAGGGTGA	90678
rs13284064	snp	C/T	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127481746	TAGATATATAATGTC[C/T]AACTATATTCCTAGT	90678
rs13292407	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127495135	tttgtatttttagta[C/G]aggtggggggtttct	90678
rs28654608	snp	A/C	0.493201	0.0579089	intron-variant	LRSAM1	GRCh38.p7	9:127458399	GTCTCAAAAACAAAA[A/C]AAAACAAAACAAAAC	90678
rs33984050	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127491008	CAAGCACGTCCATGC[-/A]CCCAGGAACGCGAGG	90678
rs34004486	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127454845	AGCTCTGGGAAAGCA[-/G]GGGGTCATTGGTTCA	90678
rs34060409	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127486463	CAGGAGCCCCAGACA[-/G]GGGACAGGCCAGCAG	90678
rs34143968	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127498692	CGTCCTCAGTTCCAG[-/T]AAGGCAAGGGAAACC	90678
rs34221235	in-del	-/C			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452459	GAGCTGCCATCTTTG[-/C]CCCATCCCTCTGAGG	90678
rs34232789	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127461886	CATATGAGTAATGAG[-/A]AACAACAGTGGCGCC	90678
rs34253813	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127464934	GTGTGAGCCACCACA[-/C]CCCAACCTGGACACT	90678
rs34281811	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127493353	GGCATGAGCCACCGC[-/G]GCCTAGCCTCTCCTG	90678
rs34371145	in-del	-/AGT/TAG			intron-variant	LRSAM1	GRCh38.p7	9:127456413	AATTTTTGTATTTTT[-/AGT/TAG]AGAGATGAGGTTTTG	90678
rs34376189	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127463536	TCTTCACCTCATCTT[-/C]CCCTGTGTACATGTC	90678
rs34421011	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127472322	TATATATGTGTGTGT[-/A]AAAATTTGTTTTTTG	90678
rs34426300	snp	A/G	0.0038262	0.0435713	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489464	GATGCAGAAGGCTGC[A/G]TTCGAGGCACTCCAG	90678
rs34427790	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127474807	ACAAGCTAGCACAGG[-/C]ACGACACAGAGGAGG	90678
rs34459766	in-del	-/AA	0.49706	0.0382258	intron-variant	LRSAM1	GRCh38.p7	9:127456163	TAAATGAGAATATGC[-/AA]AAAAAAAAAAAAAAA	90678
rs34598808	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127455300	CTCCTACATTGCTGG[-/T]AAGGGCCTGGCATTC	90678
rs34768188	snp	C/T	0.0064377	0.0563685	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502884	CCAGCGCCTCCGCAT[C/T]TACCACAGCAGCTGA	90678
rs34940320	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127499530	AGCAAGACCCTGTCT[-/A]AAAAAAAATATATAT	90678
rs34968274	in-del	-/T	0.493613	0.0561475	intron-variant	LRSAM1	GRCh38.p7	9:127453432	AAATGGAATAATAAC[-/T]GAGGGTGGTAAGCTG	90678
rs35025231	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127478848	AGTTTGTATAACATC[-/A]AGGCCACCCGGGGGT	90678
rs35106166	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127501159	TAAGTCCGGGGCCCT[-/C]CCCCACCCGCCTGCC	90678
rs35181083	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127463199	GCAAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA	90678
rs35548576	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127479808	TCTGAGGGGGTCCCA[-/G]GGGGCTCAGGACCCC	90678
rs35636470	snp	A/G	0.133777	0.221342	intron-variant	LRSAM1	GRCh38.p7	9:127458384	ACAGAGCGAGACTCC[A/G]TCTCAAAAACAAAAC	90678
rs35712163	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127475907	ACCATGCCCGGCTAA[-/T]TTTTGTATTTTTAGT	90678
rs35821814	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127476933	CACTTGTCTCAGCCT[-/C]CCCAAAGTGCTGGGA	90678
rs35834839	in-del	-/T/TT	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127484263	TTGAATTTCTTTCCC[-/T/TT]TTTTTTTTTTTTTTT	90678
rs35854322	in-del	-/G			frameshift-variant, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459050	CCTTCCTGACGATCT[-/G]GGGCAGCTGACTGCC	90678
rs35907765	snp	A/G	0.0930568	0.194599	intron-variant	LRSAM1	GRCh38.p7	9:127458439	AAAAACACCAGCAGA[A/G]CATGTTGGCTTGTGC	90678
rs36092041	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127465157	CACAGCCCCAGGACA[-/C]TAAGGGGCCTGATTA	90678
rs41313847	snp	A/G	0.0433465	0.140692	intron-variant	LRSAM1	GRCh38.p7	9:127493948	AGACCAGCTGCTTCT[A/G]GAGCCCTGAACAAGC	90678
rs55828933	snp	A/G	0.101584	0.201179	intron-variant	LRSAM1	GRCh38.p7	9:127489410	GAAAAGTGTGGGCAC[A/G]GCCCCTGCTGAGGGC	90678
rs55926522	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127470131	TCAAATATCCTATGG[C/G]CCATGAGTTCCATTC	90678
rs56043611	in-del	-/CA			intron-variant	LRSAM1	GRCh38.p7	9:127468835	AAAAAAAAAAAAAAA[-/CA]AAAATCAGCCAGGCG	90678
rs56131876	snp	A/G	0.0678174	0.1712	intron-variant	LRSAM1	GRCh38.p7	9:127479598	CGGATGTGGAAAGGC[A/G]GTGGGATGAAGCTGT	90678
rs56141720	snp	C/T	0.00882472	0.0658368	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452325	GTCATCAGGGACGGA[C/T]GGGGGAGGGCTGTTT	90678
rs56160932	snp	C/T	0.0166325	0.0896639	intron-variant	LRSAM1	GRCh38.p7	9:127479772	GCCAGCCTCCTAACC[C/T]CAGTCAGTACCCCTC	90678
rs56261604	snp	A/G	6.73605e-05	0.00580308	intron-variant	LRSAM1	GRCh38.p7	9:127479517	GGAGGTTTGTGAGCC[A/G]CCTGCTAGGGTCCAG	90678
rs56288234	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127475801	GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC	90678
rs56380300	snp	A/G	0.00746321	0.0606293	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479900	TCAACGCAGAGCGGC[A/G]GCGGCTGCAGGAGCA	90678
rs56702056	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127456708	TCTCTACCAAAAATA[A/C]AAAAAAAATCAGCTG	90678
rs56957982	in-del	-/CA	0.396364	0.202676	intron-variant	LRSAM1	GRCh38.p7	9:127479095	CCTTCCTCTTACACG[-/CA]CAGTCTGCTGCATCC	90678
rs57605811	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127468401	GCACAGCAGAAGGAG[C/T]TAAAACCCGGAGCCA	90678
rs57829212	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127456718	AAATAAAAAAAAAAT[C/T]AGCTGGGTGTGGTGG	90678
rs57954435	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127456675	CAAGACCATCCTGGC[C/T]ACCATGGTGAAACCC	90678
rs58140930	in-del	-/TT/TTT	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127460873	TTTTTTTTTTTTTTT[-/TT/TTT]GAGACGGAGTCTCAC	90678
rs58385996	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127456677	AGACCATCCTGGCTA[A/C]CATGGTGAAACCCGG	90678
rs58468837	in-del	-/C/CA			intron-variant	LRSAM1	GRCh38.p7	9:127468834	AAAAAAAAAAAAAAA[-/C/CA]AAAAATCAGCCAGGC	90678
rs58490422	in-del	-/C/CT/TT			intron-variant	LRSAM1	GRCh38.p7	9:127484808	TGATTTTTCTTTTTT[-/C/CT/TT]TCTTTTTTTTTTTTT	90678
rs58675082	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127466609	CCTCCCACCTTGGCC[C/T]CCCAAAGTGCTGGGA	90678
rs58690821	in-del	-/TTTTTTTTTT			intron-variant	LRSAM1	GRCh38.p7	9:127460864	TTTTTTTTTTTTTTT[-/TTTTTTTTTT]GAGACGGAGTCTCAC	90678
rs59149685	in-del	-/T	0.492727	0.0598633	intron-variant	LRSAM1	GRCh38.p7	9:127499539	CTGTCTAAAAAAAAA[-/T]ATATATATATATATA	90678
rs59194012	snp	A/G	0.0329836	0.124112	intron-variant	LRSAM1	GRCh38.p7	9:127462949	TCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAA	90678
rs59448492	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127474386	GATCCTCCCACCTCA[A/G]ACTCCCAAAGTGCTG	90678
rs59466573	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127456727	AAAAATCAGCTGGGT[A/G]TGGTGGCATGCGCCT	90678
rs59501881	snp	C/T	0.00366971	0.0426777	intron-variant	LRSAM1	GRCh38.p7	9:127481174	GACCTTTTATGATTT[C/T]CTCCACAGACAAAAG	90678
rs59552786	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127498852	TCACCTGAGGTCAGG[A/C]GTTCGAGACCAGCCT	90678
rs59666107	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127456684	CCTGGCTACCATGGT[A/G]AAACCCGGTCTCTAC	90678
rs59881288	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127468527	CCAAGACACACATGC[C/T]TATGACTTATCATGG	90678
rs60012839	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127466500	TATATATATATATAT[-/A]TATATTTTTTTTTTT	90678
rs60202040	snp	A/T	0.429238	0.174281	intron-variant	LRSAM1	GRCh38.p7	9:127499541	GTCTAAAAAAAAATA[A/T]ATATATATATATATA	90678
rs60638327	in-del	-/TT			intron-variant	LRSAM1	GRCh38.p7	9:127456646	AGGTGGGCAGATCAC[-/TT]GAGGTCAGGAGATCA	90678
rs60659104	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127474535	CACAGTTCCTTGGTA[G/T]CACTTATCACAGCGC	90678
rs60750457	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127466498	TATATATATATATAT[-/A]TATATATTTTTTTTT	90678
rs61016254	snp	G/T	0.0345262	0.126772	intron-variant	LRSAM1	GRCh38.p7	9:127479043	AATATTTGAGAAAAT[G/T]ACTTCTTCCCAGCTC	90678
rs61032058	in-del	-/ATATATATTTT			intron-variant	LRSAM1	GRCh38.p7	9:127466505	TATATATATATATAT[-/ATATATATTTT]TTTTTTTTTTTTTTT	90678
rs61211444	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127456683	TCCTGGCTACCATGG[C/T]GAAACCCGGTCTCTA	90678
rs61386144	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127456661	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	90678
rs61393400	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127459892	GAATTGCTGCATTCA[C/G]TAATTTGTAACTTTT	90678
rs61568854	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127483180	GGCTCTGGGGTCAGC[A/C]TAGATGTGGATGCAG	90678
rs61599642	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127456625	ATCCCAGCACTTCGG[C/G]AGGCCGAGGTGGGCA	90678
rs61636754	snp	C/T	0.0158469	0.0875917	intron-variant	LRSAM1	GRCh38.p7	9:127472759	AGTCTTGGGTATTTT[C/T]CTGTCTCATAGTACG	90678
rs62584966	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127459214	TCCCCTTGGCCCTTT[G/T]GGGTTTTTTTTTTTT	90678
rs62584967	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127466359	TAACCCAAAATCTCC[C/T]TTTAGAGGAAACCAC	90678
rs62584994	snp	A/G	0.427879	0.175668	intron-variant	LRSAM1	GRCh38.p7	9:127472315	TATATATATATATAT[A/G]TGTGTGTAAAATTTG	90678
rs62584995	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127474828	ACAGAGGAGGAAGCT[C/T]AAAGGGTTTGCCACA	90678
rs62584996	snp	G/T	0.433963	0.169285	intron-variant	LRSAM1	GRCh38.p7	9:127485076	GCTTCCCAAAGTGCT[G/T]GGATTACAGGCATAA	90678
rs62584997	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127491947	CGGAGGGCTGGATGG[A/G]ATGGTGTGTGAGGAC	90678
rs62584998	snp	G/T	0.455977	0.141681	intron-variant	LRSAM1	GRCh38.p7	9:127500155	CACCTGAAGTCAAAA[G/T]CTTGAGACCAGCCTG	90678
rs67841124	in-del	-/CTAT/TATC			intron-variant	LRSAM1	GRCh38.p7	9:127490092	TGCTGACCTTCAAGC[-/CTAT/TATC]CTTGGGCAAGCCCAC	90678
rs67903079	in-del	-/A	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127499538	CTTGTCTAAAAAAAA[-/A]TATATATATATATAT	90678
rs68012879	in-del	-/AG	0.341012	0.232845	intron-variant	LRSAM1	GRCh38.p7	9:127489557	TGGACCTGCTCTCTC[-/AG]AGACTTGCAGAGTGG	90678
rs68128813	multinucleotide-polymorphism	AAC/CAA	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127458417	AACAAAACAAAACAA[AAC/CAA]AAAAAAAAACACCAG	90678
rs71380063	in-del	-/GGCCACTGGCCACGTGTATCTATTGAGCACCTGGAGACCGTGCTGTCCAGAGCGGC	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127464384	GCTGTCCAGAGCGGC[lengthTooLong]AGCCGCTGGCCATAT	90678
rs71380064	in-del	-/A	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127471497	AAAAAAAAAAAAAAA[-/A]GATTTTGGGCTGGGC	90678
rs71380065	in-del	-/AAA	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127475495	ATGAGACTCCATCTC[-/AAA]CAAACAAACAAACAA	90678
rs71380066	in-del	-/A	0.375	0.216506	intron-variant	LRSAM1	GRCh38.p7	9:127502710	AAAAAAAAAAAAAAA[-/A]GACGGGCCTGGGACT	90678
rs71494054	in-del	CTGTCTA/TTGTCT	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127499524	TGACAGAGCAAGACC[CTGTCTA/TTGTCT]AAAAAAAATATATAT	90678
rs71494055	in-del	CTGTCTCAAAAA/GTCTC	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127500354	TGACAGAGCGAGACT[CTGTCTCAAAAA/GTCTC]AAAAAAAAAAAAAAA	90678
rs71497654	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127456134	ATGGGTAGAAGCGCT[C/T]TAAGTGAAGTATCTA	90678
rs71497655	snp	A/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127459091	GGCTGCAGAAACAGA[A/T]ACCCACCTCGGATGG	90678
rs71497656	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127463353	GTGATATGGGGCCCA[A/G]AAAGCTGGGAGGGAG	90678
rs71497657	snp	G/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127471010	GAGAGAAAGATTTTG[G/T]GCTCTTTTCTGTATG	90678
rs71497658	snp	A/G	0.5	0	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479893	CGCCACCTCGACGCA[A/G]AGCGGCAGCGGCTGC	90678
rs71497659	snp	G/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127481815	AATCCCAGCACTTTG[G/T]GAGGCCGAGGTGGGC	90678
rs72039948	in-del	-/TTT			intron-variant	LRSAM1	GRCh38.p7	9:127460871	TTTTTTTTTTTTTTT[-/TTT]TTGAGACGGAGTCTC	90678
rs72767940	snp	A/C	0.00478085	0.0486577	intron-variant	LRSAM1	GRCh38.p7	9:127462615	AAGAATGCTGAATCC[A/C]GAAGAGGCTGACACT	90678
rs72767947	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127470463	TCCCGCCCCCAACAC[A/G]TGGGGATTACAATTC	90678
rs73590852	snp	G/T	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127482523	AACATTCTGCCAGTT[G/T]ACACTCCTCTCAGCA	90678
rs73590855	snp	G/T	0.0341408	0.126114	intron-variant	LRSAM1	GRCh38.p7	9:127485611	TAAGATAACTATCAG[G/T]TAGGTAACCAGGTGA	90678
rs73590858	snp	C/G/T	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127488207	CTTGAGTGGATGAAA[C/G/T]GAAGGGCCCCTGTGA	90678
rs74221595	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467147	CCTGAGGAAGGGGCT[A/G]GTTTTGTTTTTATAC	90678
rs74310357	snp	A/G	0.256897	0.249905	intron-variant	LRSAM1	GRCh38.p7	9:127482136	AGCAGAATTTTTAGT[A/G]TATCTTTTTTTTTTT	90678
rs74472939	snp	A/C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458824	AAATAAGAAAATGGT[A/C/G]TAATGGTTTGAGAAG	90678
rs74550869	snp	C/T	0.0475351	0.146656	intron-variant	LRSAM1	GRCh38.p7	9:127496515	CTTCAAAACAGAATA[C/T]TCATCGCTGTGCCAG	90678
rs74696201	snp	C/T	0.0869089	0.189476	intron-variant	LRSAM1	GRCh38.p7	9:127476680	GATGGAATTGTTTTC[C/T]TTTTTCTTTTTGAGA	90678
rs74741433	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127484905	CTCTGCCTCCCGGGT[G/T]CAAGCGATTCTCCTG	90678
rs74876850	snp	C/T	0.00231922	0.033974	intron-variant	LRSAM1	GRCh38.p7	9:127454644	ATCCCATCTCCTCCT[C/T]GGTCCCCATGGAGTA	90678
rs74894027	snp	A/C	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127462112	CTTGAACTGGAACTC[A/C]ACCTTCTTGAGCCTA	90678
rs75130020	snp	C/G	0.039522	0.134904	intron-variant	LRSAM1	GRCh38.p7	9:127462506	GGCATGGTCCTTGGA[C/G]GCTTGTAGAGAGGCC	90678
rs75171318	snp	C/T	0.0343608	0.12649	intron-variant	LRSAM1	GRCh38.p7	9:127496101	CCTGGCCAAGGTGGG[C/T]AGCAGCCGTCTGCAT	90678
rs75255365	snp	C/T	0.0185279	0.0944493	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450696	TTAAAGTGAAACAAA[C/T]GTGAAAAAAATGCCC	90678
rs75406328	snp	A/C	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127476578	AAGAAAACTCAAAAC[A/C]AAAAAAGGAAACAGA	90678
rs75608566	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127478460	TGCACCATGACTTAC[A/G]GACAGATGTTGATAG	90678
rs75663017	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127454710	CCCATCTGCCTCCCC[C/G]ACCCACAGAAGAAAT	90678
rs75690855	snp	C/T	0.0269683	0.112946	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467759	TGAGCCTTGACGCCT[C/T]GGCCATGGTCTACCC	90678
rs75884543	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127484904	CCTCTGCCTCCCGGG[A/T]TCAAGCGATTCTCCT	90678
rs75945869	snp	A/G	0.0482946	0.147699	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450158	CAAGGAAGAATAGTT[A/G]AGATACAGGTTAAAA	90678
rs76153575	snp	G/T	0.00256417	0.0357143	splice-donor-variant	LRSAM1	GRCh38.p7	9:127473933	AGTTAGAGTGGCAGG[G/T]AAGACAAGGCAGCCT	90678
rs76376186	snp	C/T	0.0475351	0.146656	intron-variant	LRSAM1	GRCh38.p7	9:127500761	AGAGATCAGAGGACC[C/T]ACTTAACAAGCGCTG	90678
rs76406733	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127478918	TCTCTTGACCACTGT[C/T]TTTTTTTCCTCCCAG	90678
rs76446834	snp	A/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127490655	AGTTTTCTTGTCTAT[A/T]AAATGGAGGCAATAA	90678
rs76563060	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127476085	TGATCCAGAAGTTCC[A/G]CTTCTCAATGTATAC	90678
rs76576041	snp	A/G	0.0314385	0.121371	intron-variant	LRSAM1	GRCh38.p7	9:127495796	GGCAGTGAACCCCTG[A/G]GCCTATCTATCTATC	90678
rs76654972	snp	A/G	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127486022	ATGATTCAGTGTTGG[A/G]CTGTGTTAAAGTGGT	90678
rs76703521	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489232	TGGAAACTCAGGGTG[C/T]GATGCCGGAAGTGCA	90678
rs76825439	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127479098	TTCCTCTTACACGCA[C/G]TCTGCTGCATCCTCA	90678
rs76870511	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467407	AAGTGCATTCCTGGA[C/T]GTGCTTTGAGTCAGT	90678
rs76922504	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127483448	CGAGACCATTTCTCA[A/G]AAAAAAAAAAAAAGA	90678
rs76938050	snp	A/G	0.021333	0.101051	intron-variant	LRSAM1	GRCh38.p7	9:127492169	TTCTTCCCCTACTCC[A/G]TAAGATGGCAGCGGT	90678
rs77035202	snp	A/G	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127479774	CAGCCTCCTAACCCC[A/G]GTCAGTACCCCTCAC	90678
rs77216722	snp	A/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127470986	CACTTGACTAATCTT[A/T]AAAAAAGAGAGAGAA	90678
rs77254291	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127479095	GCCTTCCTCTTACAC[A/G]CAGTCTGCTGCATCC	90678
rs77256629	snp	G/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127483319	AGGTGTCGGGGCTCA[G/T]GCCTGTAATCCCAGC	90678
rs77285815	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127490274	TTTCTTTCTTTCTTT[C/T]TTTTTTTGGACCAAT	90678
rs77464345	snp	C/T	0.0162398	0.0886349	intron-variant	LRSAM1	GRCh38.p7	9:127466951	CGAGACTGCAGTGTT[C/T]GTGCCACTGCACTCC	90678
rs77495522	snp	C/G	0.0869089	0.189476	intron-variant	LRSAM1	GRCh38.p7	9:127470963	TCTTTCTCCTCTTCT[C/G]ACCGCTGCACTTGAC	90678
rs77669863	snp	A/G	0.00835141	0.0640778	intron-variant	LRSAM1	GRCh38.p7	9:127496732	GGCCCCAGAGTTCGT[A/G]TTCTTTTTCATGAGA	90678
rs77755593	snp	C/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127458911	TTCTGCACTGGGGGT[C/G]TGAGGTGGCCCCAGC	90678
rs77998194	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127482659	TTACCAGTAATGTTA[A/G]GCATCTTTCCAGATG	90678
rs78037809	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454346	CCAGCCGCTGCCTCC[A/G]TGGAACTCACTAGGG	90678
rs78092332	snp	A/C	0.0479149	0.147179	intron-variant	LRSAM1	GRCh38.p7	9:127460544	AGTCCCCTTCTCCCT[A/C]CTTCCCTGATGGTGG	90678
rs78101955	snp	G/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127484827	TTTTTTTTTTTTTTT[G/T]AGATAGGGTCTTGCT	90678
rs78192407	snp	C/T	0.0825414	0.185628	intron-variant	LRSAM1	GRCh38.p7	9:127457857	ACCTTCAGAGGAGGC[C/T]GGCAGCACAGGTGTC	90678
rs78209339	in-del	-/AAAGA			intron-variant	LRSAM1	GRCh38.p7	9:127471495	AAAAAAAAAAAAAAA[-/AAAGA]TTTTGGGCTGGGCGC	90678
rs78236680	snp	A/C	0.0399052	0.1355	intron-variant	LRSAM1	GRCh38.p7	9:127497551	TGGGAGAACAGGAGA[A/C]CTCCACGTAGCAGTG	90678
rs78283142	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450525	CAGCAGTGGAGACAC[A/G]TGGAGCTAATTACAA	90678
rs78292262	snp	A/G	0.0189856	0.0955633	intron-variant	LRSAM1	GRCh38.p7	9:127461649	GAGTCCACTGGGCAG[A/G]CTGAGGGCAGTGGTG	90678
rs78586507	in-del	-/A/ATT	0.00953873	0.0683987	intron-variant	LRSAM1	GRCh38.p7	9:127475073	ATTATTATTATTATT[-/A/ATT]TTATAGTTCAGCAAG	90678
rs78732326	snp	A/G	0.0387552	0.1337	intron-variant	LRSAM1	GRCh38.p7	9:127474789	GCCCTGTCAGGTCCT[A/G]GCGACAAGCTAGCAC	90678
rs78763712	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127497432	TTCAGGATGACTCCT[A/G]AGGGCTGGTTCTAGC	90678
rs78767255	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127492438	AGGCTCTGGTTTGCA[C/T]GCACCTCCATTTGTG	90678
rs78811984	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127461894	GTAATGAGAACAACA[A/G]TGGCGCCCCATTGCT	90678
rs79065754	snp	A/C	0.0869089	0.189476	intron-variant	LRSAM1	GRCh38.p7	9:127478687	CCAGAACTGTCTTGA[A/C]GAGCCCCTCCTACAG	90678
rs79075038	snp	C/T	0.0402882	0.136092	intron-variant	LRSAM1	GRCh38.p7	9:127473505	GAGCTGGATCTAGGA[C/T]GCAGGTTTCACTGCT	90678
rs79186916	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127492748	ATCCTGCCACTGCGG[C/G]ACTCCTGCGCTGCCG	90678
rs79346071	snp	A/G	0.0475351	0.146656	intron-variant	LRSAM1	GRCh38.p7	9:127468432	GCACTGGCTGGAGGC[A/G]GGAGGAGAGCAGGAT	90678
rs79366656	snp	A/G	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127491075	GAGGTTCCCAGGCCC[A/G]CAGGTTCCCCTCATT	90678
rs79463842	snp	A/G	0.00438332	0.0466095	intron-variant	LRSAM1	GRCh38.p7	9:127470182	GTCTGTTCTCACACC[A/G]CTATGAAGAAATTCC	90678
rs79514284	snp	C/T	3.30316e-05	0.00406383	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459044	GACAGCCCTTCCTGA[C/T]GATCTGGGGCAGCTG	90678
rs79662728	in-del	-/T/TAG			intron-variant	LRSAM1	GRCh38.p7	9:127456415	TTTTTGTATTTTTAG[-/T/TAG]AGATGAGGTTTTGCC	90678
rs79960557	snp	C/T	0.00835141	0.0640778	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453647	CTGAGGAAACGTCTC[C/T]AAGTTTCCCTAGAAC	90678
rs80079018	snp	C/T	0.00953873	0.0683987	intron-variant	LRSAM1	GRCh38.p7	9:127471111	GCAAATTAGAGTCTT[C/T]GAGCAACAGGTGATT	90678
rs80153391	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127467372	GCTGCTGGTGCAGCT[C/T]ACCTCAATATCTTAT	90678
rs111301203	snp	C/T	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127484199	CTTTTGTGTCTACCA[C/T]ATTTCACTTAGCATA	90678
rs111395795	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127463815	CTCACCTTTATCTGG[A/G]GCTTTCTAAGACTGG	90678
rs111496878	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127487843	TGCAGAGCTCCACAC[A/G]GAGCCCTTCCTAGAC	90678
rs111564851	snp	A/G	0.0869089	0.189476	intron-variant	LRSAM1	GRCh38.p7	9:127492108	GGTCTCAGGTGCACC[A/G]CAGGTGTGCTGTGTG	90678
rs111575097	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127465303	GTGCAGCCAACATGG[A/C]CACCCCAGCCACTTG	90678
rs111662869	snp	C/T	0.00137248	0.0261602	intron-variant	LRSAM1	GRCh38.p7	9:127497206	GCTCACACCATTTAG[C/T]GGGCTCCCGCCCAGG	90678
rs111669564	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127484339	TTCTTCCTTTTTAAT[A/G]GTAAATAACGTTGCA	90678
rs111718850	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449715	TTTTGGAGACTAGAA[A/G]TAAAGGCATGTAATC	90678
rs111724344	in-del	-/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127488600	TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTAAG	90678
rs111740531	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127465860	CAACACAACTCACAC[C/T]GTGGATGGGGCAGTT	90678
rs111752827	snp	A/G	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127477692	GAGGTCGCGGCTGCA[A/G]TGAGCTGAGATTGTG	90678
rs111756778	snp	G/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127497735	GGACATGGAGAGATG[G/T]CCACAACAGGCTGTG	90678
rs111789825	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491000	TGGCCACAACAAGCA[C/T]GTCCATGCCCCAGGA	90678
rs111823259	in-del	-/T	0.47709	0.104548	intron-variant	LRSAM1	GRCh38.p7	9:127474261	CTTATCCTTCAGTTC[-/T]TTTTTTTTTTTTTTT	90678
rs111841854	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127457251	TGGGCTGGCTCCCAC[A/G]CCCTTAGCCTGCCCT	90678
rs111850696	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127489627	CCCCAGCTCCTTGGC[C/T]TGCTAGCCCAACAAG	90678
rs111869310	in-del	-/AGA	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127500847	TGAGGCTCAGAGAAG[-/AGA]AGAAGAGAGTGTGTG	90678
rs111895579	snp	A/C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472531	CTATAATCCCAGCTA[A/C/T]TCAGGAGGCTGAGGC	90678
rs111915609	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127456002	ACCACGTAGTAAAGG[C/T]TTATGAACCCCGGTG	90678
rs111920763	snp	A/G	0.444444	0.157135	intron-variant	LRSAM1	GRCh38.p7	9:127473447	CATGGCCAGAGAAGG[A/G]AAGCATCTTGCCCAA	90678
rs111930226	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127485606	TTTTTTAAGATAACT[A/G]TCAGGTAGGTAACCA	90678
rs111988501	snp	C/T	0.448452	0.152042	intron-variant	LRSAM1	GRCh38.p7	9:127471677	CTGTAATCCCAGCTA[C/T]TCAGGAGGCTGAGGC	90678
rs112119803	in-del	-/C	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127485439	GCAGGCGTCTGTAGT[-/C]CCAGCTACTCGGGAG	90678
rs112268681	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127495421	CTTGAAGCTGCAAGT[A/G]AGGACTGCTGGTGCC	90678
rs112275975	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127483989	TATATTAGTTCTGTG[A/G]CATTATTGTTGTACA	90678
rs112336153	snp	A/T	0.039522	0.134904	intron-variant	LRSAM1	GRCh38.p7	9:127456878	CTCAAAAAAAAAAAA[A/T]AAGAAAAGGAAAAAT	90678
rs112364362	in-del	-/A	0.450483	0.149354	intron-variant	LRSAM1	GRCh38.p7	9:127465996	TGTATATTGTAAAAC[-/A]AAAAAAAATGCAAAT	90678
rs112370760	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127492309	TCTCAGAGAAGCTGC[A/G]GTCATCATGCCTGGC	90678
rs112428239	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127471756	CTCGCCACTGCACTC[C/T]AGCCTGGGCGACAGA	90678
rs112435797	snp	A/C/T	0.00149826	0.02733	intron-variant	LRSAM1	GRCh38.p7	9:127457443	GCATGGGGTTCCACG[A/C/T]GGCAGCTGAGCGCCT	90678
rs112460990	snp	C/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127486178	CAGGTTCTGAGAAAC[C/T]GTATAACGCACCCAA	90678
rs112522307	in-del	-/A	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127499056	GTGAAACTCTGTCTC[-/A]AAAAAAAAAAAGAAA	90678
rs112531092	snp	C/T	0.0391387	0.134304	intron-variant	LRSAM1	GRCh38.p7	9:127466005	GTAAAACAAAAAAAA[C/T]GCAAATATTAAGAAA	90678
rs112616717	snp	G/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127457963	TCACTACAGATGCTT[G/T]CTTTCTTTTTTTTTT	90678
rs112619826	snp	A/G	0.0887219	0.191022	intron-variant	LRSAM1	GRCh38.p7	9:127477770	AAACTTGTGTGGGCC[A/G]GGCGCAGTGGCTCAT	90678
rs112632172	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467194	GAGGGGGGAGTTTAG[C/T]TGAAGCAATTTTTAC	90678
rs112646534	snp	C/T	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127502574	CGCCTGTAGTCCCAG[C/T]TACTTGGGAGGCTGA	90678
rs112728877	snp	A/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127475749	TTTTATTATTTTTTT[A/T]TTTTTTTTTGAGATG	90678
rs112732400	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127494861	CAGCCTGGGTGACAG[A/G]GCAAGAGTCCATCTC	90678
rs112766861	in-del	-/A	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127462648	AAGAAAGTTGTCGGT[-/A]GGGGAACAACACAGT	90678
rs112788447	in-del	-/TG	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127472314	ATATATATATATATA[-/TG]GTGTGTGTAAAATTT	90678
rs112807459	snp	G/T	0.0865458	0.189163	intron-variant	LRSAM1	GRCh38.p7	9:127475342	CTGAAAATGCAAAAC[G/T]TAGCCAGGCATGGAG	90678
rs112833023	snp	C/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127500457	CAGCCAGCATGCTGG[C/G]GACTCTGTGGGGCTG	90678
rs112857124	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127497192	GCCTGTGCCACGTGG[C/T]TCACACCATTTAGCG	90678
rs113001047	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127501256	TCTCTAAGTAGACTG[C/T]GCTCATCTAGAAAGA	90678
rs113001899	snp	A/G	0	0	intron-variant	LRSAM1	GRCh38.p7	9:127482690	TTTATTGATCACTTG[A/G]ATTTCAGCATTGGCT	90678
rs113022868	snp	C/T	0.0154538	0.0865337	intron-variant	LRSAM1	GRCh38.p7	9:127489647	AGCCCAACAAGAGGT[C/T]GAGGCCTTGCCCTCA	90678
rs113052336	snp	C/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127457182	TTCATGATACTGACC[C/T]GCATCCCCGTGGTGG	90678
rs113253813	snp	A/G	0.0414363	0.137845	intron-variant	LRSAM1	GRCh38.p7	9:127498834	GAGGCTGAGGTGGGC[A/G]GATCACCTGAGGTCA	90678
rs113268454	snp	A/C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127455173	GAAGCTCTAGTCACG[A/C/T]GATGTTTCCTTAGAT	90678
rs113307353	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127497837	TGAGCATGATCTGGG[A/G]GCCCGGCACCTGCCC	90678
rs113336550	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127459333	AAGCGATTCTCCTGC[C/G]TCAGCCTCCCTAGTA	90678
rs113364326	snp	C/T	0.00953873	0.0683987	intron-variant	LRSAM1	GRCh38.p7	9:127470738	GTCTCACAAACAATG[C/T]GGAGTGTGAGGAGCC	90678
rs113393396	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127485979	GGGCAAGTGATGGCT[A/G]CTCTTCCTGAGTTTT	90678
rs113398950	snp	A/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127501396	AAAATTTCCCAAATC[A/T]TGAAATATCAACAAC	90678
rs113425232	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127480437	AGACATGGCGCCAGA[A/G]AAGCCTGAGAAGTCT	90678
rs113472184	snp	A/G	0.0626037	0.165477	intron-variant	LRSAM1	GRCh38.p7	9:127456523	GGTGTGAGCCACCAC[A/G]CCCAGTCTGTGCTGG	90678
rs113477665	snp	A/G	0.0872718	0.189788	intron-variant	LRSAM1	GRCh38.p7	9:127472252	GGCGTGAGACACCAC[A/G]CCTGGCCAAGAAATA	90678
rs113509423	snp	G/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127496455	GAGCCCCTGTTCCTT[G/T]CTGGGCACAAGCTGA	90678
rs113551803	in-del	-/AC	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127467265	AAAAGCAGTTACAAA[-/AC]AAATAAACAGTTCCA	90678
rs113655900	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127460723	TCTTCCTCAAGGGCC[A/G]GTAGGGGGAGATAAG	90678
rs113687617	snp	A/C	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127499381	TCTCAAAAACAAAAC[A/C]AAAAAATTAAAAAAA	90678
rs113716072	in-del	-/CTAT	0.45866	0.137698	intron-variant	LRSAM1	GRCh38.p7	9:127490091	CTGCTGACCTTCAAG[-/CTAT]GCCTTGGGCAAGCCC	90678
rs113782589	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127471644	ATACAAAGACTAGCC[A/G]GGCGTGGTGATGCAT	90678
rs113806052	snp	A/C	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127479097	CTTCCTCTTACACGC[A/C]GTCTGCTGCATCCTC	90678
rs113869335	snp	C/T	0.5	0	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457324	CACACAGGTGCTGAT[C/T]GTCCACACGAATCAC	90678
rs113924170	snp	A/C	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127460739	GTAGGGGGAGATAAG[A/C]GCTTGTGTGTGTAGT	90678
rs113960676	snp	A/G	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127473091	ACAAGAGAGCCCATT[A/G]TTATTCTAATGTCAC	90678
rs113964577	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127486359	GCTGATGGCTGCTCT[A/G]GGGTCCGGCTCCCTG	90678
rs113993098	snp	C/T	0.5	0	intron-variant	LRSAM1	GRCh38.p7	9:127497557	AACAGGAGACCTCCA[C/T]GTAGCAGTGGAGGGG	90678
rs113994493	snp	C/T	0.0228947	0.104514	intron-variant	LRSAM1	GRCh38.p7	9:127481927	AGGAGTGGTGGCAGG[C/T]GCCTATGGTTCCAGC	90678
rs113996142	snp	C/T	0.0252325	0.109451	intron-variant	LRSAM1	GRCh38.p7	9:127455182	GTCACGAGATGTTTC[C/T]TTAGATTTTGTTCTC	90678
rs114292197	snp	A/G	0.00517822	0.0506191	intron-variant	LRSAM1	GRCh38.p7	9:127484658	GCCGCCATGTCCAGC[A/G]TCTACATTTTCTTTA	90678
rs114314416	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449833	GGGCACCTTCTCAAT[C/T]AGAGCACAGCTATCA	90678
rs114552588	snp	G/T	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127460824	TGTGTGTGGGTTCTC[G/T]TGTCACCTCTTCCTG	90678
rs114553373	snp	C/G	0.0130921	0.0798413	intron-variant	LRSAM1	GRCh38.p7	9:127462883	AGTTGTGATATTCAA[C/G]CCAGACCTTAAAGGA	90678
rs114779914	snp	A/G	0.0182019	0.0936463	intron-variant	LRSAM1	GRCh38.p7	9:127476550	CTAGACCCTATCTCA[A/G]AAAAGAAAGAAAAAG	90678
rs114889579	snp	A/G	0.0150606	0.0854603	intron-variant	LRSAM1	GRCh38.p7	9:127486366	GCTGCTCTGGGGTCC[A/G]GCTCCCTGTGCTCAC	90678
rs114896522	snp	A/T	0.0126979	0.078662	intron-variant	LRSAM1	GRCh38.p7	9:127501774	AATTCATTAACACTT[A/T]CTCTAAAAATTACAC	90678
rs114966990	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127458072	TCCAAGGCCTTTTTT[A/G]TGCATTTTCATTTTT	90678
rs115087590	snp	A/G	0.00835141	0.0640778	intron-variant	LRSAM1	GRCh38.p7	9:127491392	TCACCAGCCCCTGGG[A/G]GTCAAGGGCTTCCCC	90678
rs115106486	snp	A/G	0.0158469	0.0875917	intron-variant	LRSAM1	GRCh38.p7	9:127458905	CTCTGTTTCTGCACT[A/G]GGGGTGTGAGGTGGC	90678
rs115226542	snp	A/G	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127470523	CCATATCAATGCCCA[A/G]TGGAAATGCATATGA	90678
rs115235082	snp	C/T	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127498536	CACTGTTTGAGTCAT[C/T]CCTGGAGCAAACAAG	90678
rs115282147	snp	A/G	0.0174175	0.0916809	intron-variant	LRSAM1	GRCh38.p7	9:127460773	TGGGTGCCCTGGCCC[A/G]GCAGGGCGAGGGGTG	90678
rs115290091	snp	A/G	0.0178098	0.0926698	intron-variant	LRSAM1	GRCh38.p7	9:127464234	GAGAAAGGGCCGGCT[A/G]GGGAGATGGGCCAAC	90678
rs115353752	snp	A/G	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127477408	TTTTATAATTCAGAG[A/G]CTGATCCTGTTCTCA	90678
rs115498195	snp	A/G	0.0505692	0.150756	intron-variant	LRSAM1	GRCh38.p7	9:127500821	CCCATTCTGCAGATG[A/G]GAAATGAGGCTCAGA	90678
rs115563889	snp	A/G	0.0475351	0.146656	intron-variant	LRSAM1	GRCh38.p7	9:127502061	GCTGCTCCGGGTTGG[A/G]ATTGTTTGTAGACTG	90678
rs115663276	snp	A/C	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127498492	TGCAGTGCCTCTGAG[A/C]CCAGCAGTCCTCAGG	90678
rs115721486	snp	A/G	0.453818	0.144769	intron-variant	LRSAM1	GRCh38.p7	9:127472317	TATATATATATATGT[A/G]TGTGTAAAATTTGTT	90678
rs115844834	snp	A/C	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450524	GCAGCAGTGGAGACA[A/C]ATGGAGCTAATTACA	90678
rs116296509	snp	C/T	0.00835141	0.0640778	intron-variant	LRSAM1	GRCh38.p7	9:127471954	AAGTGTGAGCCACCA[C/T]GCCCTGCAAGAAATA	90678
rs116297910	snp	C/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127477087	AGTAAATAGATTATA[C/T]TTGATTAAAAAAATG	90678
rs116323570	snp	C/T	0.0399052	0.1355	intron-variant	LRSAM1	GRCh38.p7	9:127498650	CCTGCTTGTGCCCAT[C/T]GGCAGGGGAAGGGGC	90678
rs116498902	snp	C/T	0.030665	0.119967	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	RPL12, LRSAM1	GRCh38.p7	9:127451542	GAGGCTGACGGCTGG[C/T]AAGCAGGGCACCGCG	90678
rs116606854	snp	C/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127473239	ACAACTTGTTTACCC[C/T]GGAAGGACACCATCA	90678
rs116715965	snp	A/G	0.0107246	0.0724382	intron-variant	LRSAM1	GRCh38.p7	9:127499925	TGAGACTCCATCTCA[A/G]AAAAAAAAAGAAAAA	90678
rs116791639	snp	A/C	0.0182019	0.0936463	intron-variant	LRSAM1	GRCh38.p7	9:127477755	TCCATCACAAAGAAA[A/C]AACTTGTGTGGGCCG	90678
rs116862814	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453957	CTAGGAAGACGCAGT[C/T]CCTGGCTCCATGGAA	90678
rs116885615	snp	C/T	0.00636936	0.0560724	intron-variant	LRSAM1	GRCh38.p7	9:127455171	CAGAAGCTCTAGTCA[C/T]GAGATGTTTCCTTAG	90678
rs116978231	snp	A/G	0.0209421	0.100162	intron-variant	LRSAM1	GRCh38.p7	9:127490584	CATCCCAGAGAAAGG[A/G]ATCTCTCCCTTACCT	90678
rs117004045	snp	G/T	0.0111196	0.0737302	intron-variant	LRSAM1	GRCh38.p7	9:127466862	AAATACAAAAATTAG[G/T]CATGGTGGCATGTGC	90678
rs117155357	snp	A/C/G	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127498611	CCACATGCAGAAAAC[A/C/G]GATGCCTGGGCTGCT	90678
rs117197911	snp	C/T	0.00858015	0.0649342	intron-variant	LRSAM1	GRCh38.p7	9:127461280	CCAAGAAGCCGTGTC[C/T]GTGTGACCCTCCATC	90678
rs117236749	snp	C/T	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127493527	CGTCCTTTCTCAAGG[C/T]TGTCCGTGGCCCCTA	90678
rs117240905	snp	A/G	0.0130921	0.0798413	intron-variant	LRSAM1	GRCh38.p7	9:127472442	AGGTCAGGAGTTCGA[A/G]ACCACCTTTACCAAC	90678
rs117245029	snp	A/G	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127495657	CACTGAGCCCACAGT[A/G]GAGCAAAGCCTGTGC	90678
rs117357538	snp	C/G	0.0165278	0.0893908	intron-variant	LRSAM1	GRCh38.p7	9:127489149	CCAGCGCCGCTGATT[C/G]ATGCCTCTGAGTGTC	90678
rs117433711	snp	A/C	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127498381	CAGACTGGAGATCAG[A/C]AGAGTTTTCCATCAG	90678
rs117446891	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450454	CTGCCCAATGTCTCT[A/G]AGCCAGTCCTAACTT	90678
rs117506176	snp	C/T	0.0225045	0.103662	intron-variant	LRSAM1	GRCh38.p7	9:127474771	AGCACCAGTGACAGG[C/T]TGGCCCTGTCAGGTC	90678
rs117528271	snp	A/G/T	0.00889112	0.0660804	intron-variant	LRSAM1	GRCh38.p7	9:127461281	CAAGAAGCCGTGTCC[A/G/T]TGTGACCCTCCATCA	90678
rs117606713	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465637	CACTCAACACCCACC[A/G]TGTGAGGGCTGGGCT	90678
rs117612613	snp	C/G	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453942	TGGAACTCCATGAAA[C/G]TAGGAAGACGCAGTC	90678
rs117692127	snp	A/G	0.00266947	0.0364364	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459018	GTTCTAGATCTCCAC[A/G]ATAATCAGCTGACAG	90678
rs117736098	snp	A/G	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127480033	CCCGTGCAGTCCCCT[A/G]AGGAGCCGGGAGGAG	90678
rs117789527	snp	A/G	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127460790	CAGGGCGAGGGGTGC[A/G]GGGGTCATCACTGTG	90678
rs117795199	snp	A/G	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127484997	ATTTTTAGTACAGAC[A/G]CAGTTTCGCCATGTT	90678
rs117926885	snp	C/T	0.0123036	0.0774623	intron-variant	LRSAM1	GRCh38.p7	9:127474704	TCACTGTCTGGGACA[C/T]ACACCCACCATGCTC	90678
rs117991222	snp	C/T	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127494527	TGGTCTGGCACATGG[C/T]ACTGTGAACATGTCA	90678
rs118002800	snp	C/T	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127473581	AGGTGTAAGGGGTAG[C/T]CAGTACCCATTGACT	90678
rs118029779	snp	C/T	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127497031	TTTCCCCCCAACCCC[C/T]GCCACACTGATTGTT	90678
rs118173574	snp	G/T	0.0170251	0.090679	intron-variant	LRSAM1	GRCh38.p7	9:127475319	AACGTAGTAAAACCC[G/T]GTCTCTACTGAAAAT	90678
rs118192084	snp	A/G	0.0193772	0.0965046	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450540	ATGGAGCTAATTACA[A/G]TTTAAAGGCACCAGG	90678
rs137858765	snp	C/T	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127497187	CCTGGGCCTGTGCCA[C/T]GTGGCTCACACCATT	90678
rs137924291	snp	C/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127460348	CCTGCTAGCCTTGCT[C/G]ACCTCGAGGTACCAC	90678
rs137987304	in-del	-/A	0.0134222	0.0808143	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450706	CAAATGTGAAAAAAA[-/A]TGCCCCTTGGAGGGG	90678
rs138001044	snp	A/G	0.000153988	0.00877328	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462318	GTACCCTCAACATCA[A/G]TGGAAACGAGATCCA	90678
rs138073330	in-del	-/A	0.00835141	0.0640778	intron-variant	LRSAM1	GRCh38.p7	9:127469674	CAGAAATAAAAAAAC[-/A]AAAAATAGGCCGGGC	90678
rs138105071	snp	C/T	6.59696e-05	0.00574286	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485794	CATCCAGATGGCCTA[C/T]GAATCTCAGAGGCAG	90678
rs138121918	snp	G/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127492264	TGTGAGCCTTGAAAT[G/T]ATCTCCAGAGATGAG	90678
rs138174053	snp	A/G	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127475257	AAATATTGGGAGGCC[A/G]AGGCTGGTGGATCAC	90678
rs138226428	snp	C/T	0.000153988	0.00877328	stop-gained, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487695	GCCGAAATGGATGAA[C/T]GATTCCAGCAGATTC	90678
rs138248316	snp	C/T	0.0916144	0.193427	intron-variant	LRSAM1	GRCh38.p7	9:127456766	AGCTACTCGGGAGGG[C/T]GAGACAGGAGAATTG	90678
rs138332665	in-del	-/AG	0.0228947	0.104514	intron-variant	LRSAM1	GRCh38.p7	9:127470992	ACTAATCTTAAAAAA[-/AG]AGAGAGAAAGATTTT	90678
rs138440517	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478128	ACATCAATAATAAAT[A/T]AATTAATTAAACACC	90678
rs138447448	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496631	AGGGTACATATCATT[A/C]TCATCATCTTTCAGT	90678
rs138506891	snp	A/G	0.0479149	0.147179	intron-variant	LRSAM1	GRCh38.p7	9:127460904	TCTGTTGCCCAGGCC[A/G]GAGTGCAATGGTGCA	90678
rs138558192	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127483217	AGTTCAAACACCCAC[C/T]ATGTGACCTTAGGGA	90678
rs138577091	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127456411	ACTAATTTTTGTATT[A/T]TTAGAGATGAGGTTT	90678
rs138642959	snp	A/G	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127501548	GCCAGCCTGGCCAAC[A/G]TGGTAAAACTCCATC	90678
rs138715791	snp	A/G	1.65184e-05	0.00287384	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485738	CATGTTCCCACAGCC[A/G]CCATGCAGCAGATGC	90678
rs138757111	snp	C/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127457708	AAGGAAGAGGAGGGA[C/T]GCGCAGGTGATCTGG	90678
rs138830549	snp	C/T	0.000115318	0.00759246	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467774	CGGCCATGGTCTACC[C/T]GCCGCGGGAGGTGTG	90678
rs138840893	snp	A/G	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127471550	CCAGCACTTTAGGAG[A/G]TCGAGGTGGGTGGAT	90678
rs138860248	snp	C/T	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127490176	GTGAGCGTCAGGCTA[C/T]GGGAGTACTCCTGCA	90678
rs138865676	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474724	CCACCATGCTCTGGG[A/T]CTAGTGAAGGAGTCA	90678
rs138895322	in-del	-/AACCTCCTG	0.0460142	0.144533	intron-variant	LRSAM1	GRCh38.p7	9:127483914	GTGATCGCCTGCCTC[-/AACCTCCTG]AAGTGCTGGTATTAC	90678
rs138899896	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127495715	GGGGACAGAGAGGCA[-/G]GTTGAAACAGCCCCC	90678
rs138964033	snp	A/G	0.0150606	0.0854603	intron-variant	LRSAM1	GRCh38.p7	9:127475448	GTGAGCTGAGATTGC[A/G]CCACTGCACTCCAGC	90678
rs139043079	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452589	CTTTGTGGCTAACAT[A/T]TATTGAGCGCTCATG	90678
rs139260397	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503489	GTGTCAATAAACCTG[C/T]CTTCAGTGCGCTTCT	90678
rs139271333	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481322	CAGTGGCACAATCTC[A/G]GCTCAGTGCAACCCC	90678
rs139344911	snp	C/T	0.000288446	0.0120058	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496037	ACCTGCCCATCTTTG[C/T]GCACCACCGCCTCTC	90678
rs139423667	snp	C/T	0.00914312	0.0669923	intron-variant	LRSAM1	GRCh38.p7	9:127476015	AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACCA	90678
rs139436676	snp	C/T	0.00636936	0.0560724	intron-variant	LRSAM1	GRCh38.p7	9:127486233	GCCAGGATTTGAGCC[C/T]GGCAGAGGGGAGGGG	90678
rs139447232	snp	C/G/T	3.315e-05	0.00407113	intron-variant	LRSAM1	GRCh38.p7	9:127485698	GTGCCCCAGGAGCAG[C/G/T]CACTCCACTCAGCTG	90678
rs139486692	snp	A/G	1.64741e-05	0.00286998	missense, splice-acceptor-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127478938	TTTCCTCCCAGAACA[A/G]GTTCTCAGACTATGA	90678
rs139554942	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127493122	GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC	90678
rs139588129	snp	G/T	0.0150606	0.0854603	intron-variant	LRSAM1	GRCh38.p7	9:127478502	ATTTCCAGTGTTTTT[G/T]CTCTTTTGAATAATT	90678
rs139660230	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127465956	CGCTGATAAACATTT[A/G]TCATTACATAATTTA	90678
rs139673739	snp	C/T	0.0130921	0.0798413	intron-variant	LRSAM1	GRCh38.p7	9:127498185	TCAGTGGGGAGGCCC[C/T]GGGGCTCCAGGGGGC	90678
rs139695483	snp	C/T	4.94254e-05	0.00497094	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455580	TCTTATCTTAGATTC[C/T]ATTTGGAGCTTTTGC	90678
rs139775018	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127468859	CCAGGCGTGGTGGCA[C/T]GTGCCTGTGTTCCCA	90678
rs139894120	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469835	CAAGGCGTGGTGGCG[A/G]GCGCCTGTAGTCCCA	90678
rs139977216	snp	A/G	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127465203	AGCATGCAATGAGCC[A/G]GGATCTGAAGCCATG	90678
rs139989209	snp	A/C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127453475	TAATTTGTATTCACC[A/C/G]CAGAGGTCTCTTTGG	90678
rs140008639	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494334	GTCATGCCAGCCCTC[A/G]CTGAACAGCTCCGTT	90678
rs140066362	snp	A/G	0.000170401	0.00922885	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492813	GCAGGAGATGATCTC[A/G]GAGCAGCGCTGGGCC	90678
rs140143823	snp	C/T	1.64781e-05	0.00287033	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462299	GGGGAGCTTCGAAGC[C/T]TGCGTACCCTCAACA	90678
rs140151379	snp	G/T	0.00013388	0.00818059	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479852	AGGAGCAGTCCCGGC[G/T]GGAGCAGGGCCTGAG	90678
rs140312054	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127496696	CACACAGCAGAGTGA[C/G]GTCTCCACCCCAAGC	90678
rs140336379	snp	C/T	0.00122274	0.0246956	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501071	GGAGCCTCCTGAGTC[C/T]GTGAGGCCATCCGCT	90678
rs140344062	snp	G/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127477224	GGTGTGGGGTGGGAG[G/T]GGAACCAGGGTTAGG	90678
rs140428632	snp	A/G	0.00874735	0.0655527	intron-variant	LRSAM1	GRCh38.p7	9:127488631	ACAAGGTCTTGCTCT[A/G]TTGCCCAGGATGAGT	90678
rs140467743	snp	C/T	5.01291e-05	0.0050062	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454543	ATGCCGCTCTTCTTC[C/T]GGAAGCGGAAACCCA	90678
rs140541609	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127495243	CAGGCATGAGCCACC[A/G]CGCCTGGCAACCATC	90678
rs140633361	snp	C/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127474809	CAAGCTAGCACAGGA[C/T]GACACAGAGGAGGAA	90678
rs140669144	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127463651	CTCCTTAAAGATGCT[A/G]TCTCCACATACAGCC	90678
rs140676708	snp	C/G	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127498923	AATTAGCCAGGCGTG[C/G]TGGCGTGCACCTGTA	90678
rs140774171	in-del	-/TAG	0.493154	0.0581045	intron-variant	LRSAM1	GRCh38.p7	9:127456412	TAATTTTTGTATTTT[-/TAG]TAGAGATGAGGTTTT	90678
rs140786088	snp	A/G	0.00811783	0.0631903	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501072	GAGCCTCCTGAGTCT[A/G]TGAGGCCATCCGCTC	90678
rs140808447	snp	A/G	0.000802713	0.0200178	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502838	GCTGCCAGCCACTGC[A/G]CACCTGCCCGCTGTG	90678
rs140809697	snp	A/G/T	0.000181204	0.00951707	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462343	GATCCAGAGATTGCC[A/G/T]CAGATGCTGGCTCAC	90678
rs140831224	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127471259	CAAGGCGGGTGGATC[A/G]CTTGAGCCCAGGAGT	90678
rs140843243	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127502277	ATAGAGAAATAGACA[A/G]CAAACTGCTAACAGA	90678
rs140951361	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127460451	CTTGGGTGGATCACA[C/T]GGCCTTAGGGCAGCC	90678
rs141016808	snp	A/G	0.00795532	0.062565	intron-variant	LRSAM1	GRCh38.p7	9:127481734	CATGAATAAGGCTAG[A/G]TATATAATGTCCAAC	90678
rs141024805	snp	C/T	0.00835141	0.0640778	intron-variant	LRSAM1	GRCh38.p7	9:127460287	ACAGGTGTTAGCCAC[C/T]GTGCCTGGCCCCCAT	90678
rs141135673	snp	A/G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473508	CTGGATCTAGGACGC[A/G/T]GGTTTCACTGCTTAT	90678
rs141227166	snp	G/T	0.0252325	0.109451	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452529	ACTATCTTCTCCCTA[G/T]CTCCTCTAGCGGGCC	90678
rs141247194	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127497496	CAGGCTTAGGGATCA[A/G]TGAGCCCATTTTACA	90678
rs141326230	snp	C/T	3.29473e-05	0.00405864	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461212	CTGATGCAGCTCCCA[C/T]GTTCCATTGGGAACC	90678
rs141353224	snp	C/G	0.00398564	0.0444627	intron-variant	LRSAM1	GRCh38.p7	9:127500140	CTGAGGTGGGCAGAT[C/G]ACCTGAAGTCAAAAG	90678
rs141382999	snp	A/C	1.65124e-05	0.00287331	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485741	GTTCCCACAGCCGCC[A/C]TGCAGCAGATGCTGA	90678
rs141428822	snp	A/G	7.59532e-05	0.00616205	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467829	GCAGTTCCTCTGCAA[A/G]GGTAAAGCCAGGCCG	90678
rs141542114	snp	C/T	0.000364196	0.0134895	missense, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495321	TTCATTCCTGGCAGA[C/T]GGAGTTAGAAGCCAA	90678
rs141557726	snp	A/T	0.00636936	0.0560724	intron-variant	LRSAM1	GRCh38.p7	9:127459933	CAATAACTCATAGCA[A/T]CCTTTGGTTCATCAA	90678
rs141597023	snp	C/T	0.00398564	0.0444627	intron-variant	LRSAM1	GRCh38.p7	9:127477932	TGGGTGCCTGTAATC[C/T]CAGCTACTCAGGAGG	90678
rs141660254	snp	A/G	0.0314385	0.121371	intron-variant	LRSAM1	GRCh38.p7	9:127484901	CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT	90678
rs141724747	snp	G/T	0.00288338	0.03786	intron-variant	LRSAM1	GRCh38.p7	9:127462217	CTGGTGATGGGGATT[G/T]GGGGTGTTGAGCTGT	90678
rs141827833	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127464777	CCTCCCAAGAGACTG[A/G]GACCACAGGTGTACC	90678
rs141852748	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475268	GGCCGAGGCTGGTGG[A/T]TCACTTGAGGCCAGG	90678
rs141910183	snp	C/T	0.0193772	0.0965046	intron-variant	LRSAM1	GRCh38.p7	9:127456259	TTTTTTGAAGACGGA[C/T]GCTCTGCTCTGTCAC	90678
rs141912153	snp	A/T	0.00136841	0.0261215	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127482992	AACCCAGGAGGAGAC[A/T]GAGAGCCTGCGGCGA	90678
rs141923716	snp	C/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127470244	AAGAAGTTTAATTGA[C/T]TCACAGTTTCACATG	90678
rs141934010	snp	A/C	0.00755907	0.0610114	intron-variant	LRSAM1	GRCh38.p7	9:127471629	CCATCTTTACTAAAA[A/C]TACAAAGACTAGCCA	90678
rs141972828	snp	C/T	0.0126979	0.078662	intron-variant	LRSAM1	GRCh38.p7	9:127468030	GTGGTTATGGGAGTG[C/T]AGTGGTGCAGCTGAT	90678
rs142085060	snp	C/T	0.0001812	0.00951667	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462342	AGATCCAGAGATTGC[C/T]GCAGATGCTGGCTCA	90678
rs142195263	snp	C/T	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127480082	CCTCTGCCCCTGCCC[C/T]GGGCTTCCCTTGTCA	90678
rs142302251	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127488510	CAGCTGATCCACCCA[C/G]CTCGGCCTCCCAAAG	90678
rs142325014	snp	C/G/T	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127455238	TTGGCCTCAATATAA[C/G/T]GTAGTCTCCAAGAGT	90678
rs142333739	snp	A/G	0.00878112	0.0656769	intron-variant	LRSAM1	GRCh38.p7	9:127457444	CATGGGGTTCCACGC[A/G]GCAGCTGAGCGCCTG	90678
rs142343329	snp	A/G	0.0182019	0.0936463	intron-variant	LRSAM1	GRCh38.p7	9:127495168	ATGTTGGTCAGGCTG[A/G]TCTTGAACTCCCGAC	90678
rs142344191	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127450261	AGAGAAATCCAAGAG[A/G]ACAGAATGACGGGGA	90678
rs142372610	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452644	GACATACATGAAGTC[A/G]CTGGATCCTCATAGA	90678
rs142386230	in-del	-/TTTA			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453071	CATCTACTTCTTCAC[-/TTTA]TTTATTTATTTATTT	90678
rs142410785	snp	C/G	0.0337553	0.125452	intron-variant	LRSAM1	GRCh38.p7	9:127472632	GGTGACAGAGCAAGA[C/G]TCCATCTCAAAAAAT	90678
rs142518628	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127476248	GAGCATTTGAGCCTC[A/G]GCTCGCTGGGACACA	90678
rs142625581	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127492324	GGTCATCATGCCTGG[C/T]GGGTGCCCTAGTCCC	90678
rs142638021	in-del	-/TGTG			intron-variant	LRSAM1	GRCh38.p7	9:127472314	ATATATATATATATA[-/TGTG]TGTGTAAAATTTGTT	90678
rs142664400	snp	C/T	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127489821	TTTGACTGCTCCAGC[C/T]GCCTCTGCTGTCCCT	90678
rs142782210	snp	A/G	0.000439677	0.0148204	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467780	TGGTCTACCCGCCGC[A/G]GGAGGTGTGTGGTGC	90678
rs142815758	snp	C/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127464422	TGAGCACCTGGAGAC[C/G]GTGCTGTCCAGAGCG	90678
rs142846298	snp	G/T	0.000399281	0.0141238	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455011	AGGCAAAAGAAGCTG[G/T]GGCAGATGACATTCT	90678
rs142906500	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127487184	GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAA	90678
rs142913281	snp	G/T	0.000153988	0.00877328	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454569	ACCCAGTGAGGAGGC[G/T]CGGAAACGCCTGGAG	90678
rs142919854	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499651	AATCTTTAGTTGTGG[C/T]CGGGTGCGGTGCCTC	90678
rs142949550	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460092	GCAATCTCCACCTCC[C/T]GGGTTCAAGCGATTC	90678
rs142958539	snp	C/T	3.32923e-05	0.00407983	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481206	AAAGCTCCGAGATTT[C/T]GAAATCGCTGGAAAA	90678
rs143021184	snp	C/T	0.02016	0.0983543	intron-variant	LRSAM1	GRCh38.p7	9:127472000	ACAGAGTCTCACTGT[C/T]GCCCAGGCTGGAGTG	90678
rs143059886	snp	A/C	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127491385	CAGCTGCTCACCAGC[A/C]CCTGGGAGTCAAGGG	90678
rs143146674	snp	A/G	0.0126979	0.078662	intron-variant	LRSAM1	GRCh38.p7	9:127474329	CTGGAGTGCAGTGGT[A/G]TGATCATAGCTCGCT	90678
rs143196192	snp	C/G	0.000724225	0.0190155	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450834	GAGTTAGTGTCTGTG[C/G]AGAGGGAGCCCCGAG	90678
rs143351404	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127499068	CTCAAAAAAAAAAAA[A/G]AAAAAGAAAAAAACA	90678
rs143479340	snp	A/G	0.000202727	0.0100659	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501139	TCGTGTGCCTGGAAC[A/G]GGAGGTAAGTCCGGG	90678
rs143482327	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457183	TCATGATACTGACCC[A/G]CATCCCCGTGGTGGT	90678
rs143516503	snp	A/G	8.68048e-05	0.00658748	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451358	ACCCGGATTCGGGAC[A/G]ACCGAAGGAAGTTGC	90678
rs143545279	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470793	ATCAGTCACCACAGA[A/G]CTTTGAACCAGCACT	90678
rs143561853	in-del	-/A	0.482979	0.0906686	intron-variant	LRSAM1	GRCh38.p7	9:127487184	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	90678
rs143595102	in-del	-/A	0.455977	0.141681	intron-variant	LRSAM1	GRCh38.p7	9:127500151	AGATCACCTGAAGTC[-/A]AAAGCTTGAGACCAG	90678
rs143604391	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127502141	CCCTGCGTGCCCTCC[A/G]GCAGGGGCCGGCGGA	90678
rs143644671	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127502154	CCGGCAGGGGCCGGC[A/G]GAATAGGCCTCCGTC	90678
rs143779858	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451182	GAAGGTCTCTGGGAG[A/G]CAGCGGCTTTAAGAG	90678
rs143859538	snp	C/T	0.00716266	0.059414	intron-variant	LRSAM1	GRCh38.p7	9:127465275	TGCCCACGATGAGAA[C/T]GCTCTATGATCTGTG	90678
rs143873939	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127467275	TACAAAAAATAAACA[-/G]TTCCAGGTGCAGGGG	90678
rs143901401	snp	A/G/T	0.00428275	0.046077	intron-variant	LRSAM1	GRCh38.p7	9:127479791	TCAGTACCCCTCACG[A/G/T]CGTCTGAGGGGGTCC	90678
rs143910539	snp	A/G	4.94205e-05	0.0049707	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461213	TGATGCAGCTCCCAC[A/G]TTCCATTGGGAACCT	90678
rs143976910	snp	C/G	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127483564	TTAGCATGTTATCAG[C/G]GGGAGTGTTCATAAA	90678
rs144015671	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127499543	CTAAAAAAAAATATA[A/T]ATATATATATATATG	90678
rs144095352	snp	C/T	9.0824e-05	0.00673823	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487682	TTCTGGCAGCATGGC[C/T]GAAATGGATGAACGA	90678
rs144097023	snp	G/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127486833	ATAAATATTTGCTAT[G/T]GTTGTGAAGCAGGGA	90678
rs144106850	snp	C/G	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127497390	CCGTATGTGTGGGCT[C/G]TGGTGGGGACAGTCA	90678
rs144116667	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127481337	GGCTCAGTGCAACCC[C/T]CGCCGCCCAGGTCCA	90678
rs144196759	snp	C/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127472794	GAATGTCCCCTTAAA[C/T]TGGTCACAGGATTTC	90678
rs144234592	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127470488	CAATTCAGAGATTGA[A/G]GTGGGGACACAGAGC	90678
rs144242155	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127456412	CTAATTTTTGTATTT[G/T]TAGAGATGAGGTTTT	90678
rs144291109	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127467610	GTAACAAGACAGTTC[A/G]GCCACCTCTGCTGTC	90678
rs144394245	snp	A/G	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127472001	CAGAGTCTCACTGTC[A/G]CCCAGGCTGGAGTGC	90678
rs144398861	snp	C/T	0.0123036	0.0774623	intron-variant	LRSAM1	GRCh38.p7	9:127469326	AATACAAAAACTAAC[C/T]GGGCATGGTGGCAGG	90678
rs144422060	in-del	-/A	0.0410537	0.137264	intron-variant	LRSAM1	GRCh38.p7	9:127468978	GCAATACCCTATCTC[-/A]CAAAAAAAAGGTTTA	90678
rs144438187	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127465959	TGATAAACATTTGTC[A/G]TTACATAATTTAAAA	90678
rs144502205	in-del	-/GAGAGG	0.00795532	0.062565	intron-variant	LRSAM1	GRCh38.p7	9:127468186	GGGAAGTTTGACAGA[-/GAGAGG]GCCAGTGTAGCTGGA	90678
rs144582822	snp	C/T	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127461641	CTCCTGAGGAGTCCA[C/T]TGGGCAGGCTGAGGG	90678
rs144645671	snp	C/T	7.61006e-05	0.00616802	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467796	GGAGGTGTGTGGTGC[C/T]GGCACTGCGGCCATC	90678
rs144681769	snp	C/T	0.0107246	0.0724382	intron-variant	LRSAM1	GRCh38.p7	9:127462450	ACATTACTGAGTGCT[C/T]GCTCTGATCTCACGG	90678
rs144724942	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493597	CTAGGCAATGCTCTC[C/T]GAATGCCTTTGTAGT	90678
rs144810034	snp	A/G	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127475653	AGTATGGGAAAACAG[A/G]TGTCCTCATAAACTG	90678
rs144896392	snp	C/G	0.00835141	0.0640778	intron-variant	LRSAM1	GRCh38.p7	9:127495211	GCCCACCTTGGCCCC[C/G]CAAAGTGCTGGGATT	90678
rs144914676	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127488600	TTTTCTTTTCTTTTC[C/T]TTTTTTTTTTTTAAG	90678
rs144960411	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469927	CCGAGATTGCGCCAC[C/T]GCACTCCAGCCTGGG	90678
rs145114464	snp	C/G/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127474309	GTCTTGCTCCATCAC[C/G/T]CAGGCTGGAGTGCAG	90678
rs145155290	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449767	CCACAGCCTTGAAAC[C/T]TGCCCACCACTTCTC	90678
rs145344907	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494438	CACCCTGAACCTCAG[C/T]TCCCTCACCTGGGAG	90678
rs145359330	snp	A/G	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127496775	TCCCTGGACAGATGC[A/G]GACACCAGGGTCCAA	90678
rs145382004	snp	A/T	0.000340558	0.0130447	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489478	CGTTCGAGGCACTCC[A/T]GGTGAAGAAAGACCT	90678
rs145703221	snp	A/T	0.0263992	0.111815	intron-variant	LRSAM1	GRCh38.p7	9:127474967	GCATTTGGCTTCATA[A/T]CTTCCACTGACTCTT	90678
rs145787857	snp	A/C					GRCh38.p7	9:127468827	AAAAAAAAAAAAAAA[A/C]AAAAAAAAAAAATCA	90678
rs145845374	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127458401	CTCAAAAACAAAACA[A/C]AACAAAACAAAACAA	90678
rs145876315	in-del	-/CAAA	0.346368	0.23068	intron-variant	LRSAM1	GRCh38.p7	9:127475494	AATGAGACTCCATCT[-/CAAA]CAAACAAACAAACAA	90678
rs145877456	snp	A/G	0.000300767	0.0122594	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127483003	AGACTGAGAGCCTGC[A/G]GCGACGTGACGTTGC	90678
rs145881988	snp	A/G	0.000102999	0.00717558	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479897	ACCTCAACGCAGAGC[A/G]GCAGCGGCTGCAGGA	90678
rs145947414	snp	C/T	0.00755907	0.0610114	intron-variant	LRSAM1	GRCh38.p7	9:127457527	CTGGGATTTGATCAG[C/T]ATGGTTTACTGGATA	90678
rs146019444	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453377	ATGAGCCACCACACC[C/T]GGCGTGTTTCTTCAC	90678
rs146079606	snp	A/G	0.000197984	0.0099475	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479424	GTTTGAACGGCGCCT[A/G]GAACTGGGGCAGCGG	90678
rs146091667	snp	C/T	0.0861826	0.188849	intron-variant	LRSAM1	GRCh38.p7	9:127467127	ATGCTCAAAATTCTC[C/T]TGGCCCTGAGGAAGG	90678
rs146106537	snp	C/T	0.000102449	0.00715638	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492812	CGCAGGAGATGATCT[C/T]GGAGCAGCGCTGGGC	90678
rs146197371	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492223	CAGGCCATCGGAGAA[G/T]GCTGAGCTAGCAAGG	90678
rs146267033	snp	C/T	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127486214	CAAGCCAGCAGGTGG[C/T]GGAGCCAGGATTTGA	90678
rs146344542	in-del	-/C	0.0189856	0.0955633	intron-variant	LRSAM1	GRCh38.p7	9:127473007	GAGTGGCTGGGAGGA[-/C]CTCTCTCCCCCTTCA	90678
rs146389427	snp	A/G	0.00597247	0.0543191	intron-variant	LRSAM1	GRCh38.p7	9:127468367	AGTTAGGAGGCTGTC[A/G]GGGTCATCCAGGAGA	90678
rs146458859	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500944	TGGGCAGGGCCACAA[G/T]GAGCCCCCAGGGGTT	90678
rs146613642	snp	A/G	8.23689e-05	0.00641698	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461190	CTTAAACGTGGAAAG[A/G]AATCAACTGATGCAG	90678
rs146642581	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503862	GATGCGGGGTTTGAG[A/G]CCCAGAAGCATCCTC	90678
rs146699997	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127463845	GGCATAACCTGGAAT[C/T]GCTCCGTGTATCGTC	90678
rs146714480	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127477052	TTCATAGAATTGTTC[A/G]CTAACATTGGGTGAA	90678
rs146763660	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127480757	CAGTGGTGTGCTCTC[A/G]GCTCACTGCAACCTC	90678
rs146824383	in-del	-/TTTC			intron-variant	LRSAM1	GRCh38.p7	9:127490247	TTTTCTTTCTCTATT[-/TTTC]TTTCTTTCTTTCTTT	90678
rs146859702	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127463433	AGGGGAGTTCTATAG[A/G]CTAGAAGTCCAAGAT	90678
rs146863168	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127484620	CCACCTTGGCCTCCC[A/G]TAAGTGCTTATATTA	90678
rs146879038	snp	G/T	0.0142736	0.0832652	intron-variant	LRSAM1	GRCh38.p7	9:127465808	GGGATGAGAGGGCCT[G/T]TGGGAAGTCAGAGGT	90678
rs146896900	snp	A/G	0.000148599	0.00861845	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450821	TGGGGGAAAAGAAGA[A/G]TTAGTGTCTGTGCAG	90678
rs146906754	snp	C/T	0.00636936	0.0560724	intron-variant	LRSAM1	GRCh38.p7	9:127489856	CAGGCAGGACTTCCC[C/T]ACTGGGAAAAGCAGC	90678
rs147025678	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127468755	CTGAGGCAGGAGGAT[C/T]TCGAGCCCAGGAGTT	90678
rs147107222	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482910	GATTCCCTGTTGGAA[A/G]TGTTAAATTTGCTGA	90678
rs147189253	snp	C/T	1.65072e-05	0.00287286	missense, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449657	CTGTAATCCTCAGGC[C/T]CTTCCAGTCACCCGT	90678
rs147205387	snp	C/T	0.000362384	0.0134559	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462325	CAACATCAGTGGAAA[C/T]GAGATCCAGAGATTG	90678
rs147267983	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127502169	GGAATAGGCCTCCGT[C/T]GCCTGTCCAGAGCGC	90678
rs147369460	snp	C/T	0.00398564	0.0444627	intron-variant	LRSAM1	GRCh38.p7	9:127478479	AGATGTTGATAGATG[C/T]ATGAGTTATTTCCAG	90678
rs147473665	snp	A/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127464475	TATGGAGCACCTGGA[A/T]TGTGGCTTGTGTGTA	90678
rs147483556	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127462464	TTGCTCTGATCTCAC[A/G]GTACCAGGGCCACAC	90678
rs147717838	in-del	-/T	0.458084	0.138567	intron-variant	LRSAM1	GRCh38.p7	9:127457968	CAGATGCTTTCTTTC[-/T]CTTTTTTTTTTTTTT	90678
rs147734401	snp	C/T	0.00102819	0.0226504	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127497282	AGCTGGCCTGCAGCA[C/T]GAGATCCTCCGGAGA	90678
rs147744543	snp	G/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127489645	CTAGCCCAACAAGAG[G/T]TCGAGGCCTTGCCCT	90678
rs147781815	snp	A/C	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127472948	GAGGGCACGAGCGCC[A/C]TAGGGTGCCTGGGAA	90678
rs147805183	snp	A/G	0.000132286	0.00813176	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501077	TCCTGAGTCTGTGAG[A/G]CCATCCGCTCCCCCT	90678
rs147843921	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127470571	TGTGCAAAAATGTTC[A/G]TAGCAGCACTATTTA	90678
rs147888501	snp	C/G	0.0103295	0.0711199	intron-variant	LRSAM1	GRCh38.p7	9:127459684	ATGCCTCAGCCTCCT[C/G]AGTATCTGGGATTAC	90678
rs147951459	snp	C/T	0.00835141	0.0640778	intron-variant	LRSAM1	GRCh38.p7	9:127456057	TTTTATTCTGGTCAC[C/T]CAGGGGAGATTCAGA	90678
rs148004933	snp	A/G	0.0418186	0.138422	intron-variant	LRSAM1	GRCh38.p7	9:127484885	ATGATCTCAGCTCAC[A/G]CAACCTCTGCCTCCC	90678
rs148059394	snp	A/G	0.00111698	0.023606	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467797	GAGGTGTGTGGTGCC[A/G]GCACTGCGGCCATCT	90678
rs148069846	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127461883	GTAACATATGAGTAA[A/T]GAGAACAACAGTGGC	90678
rs148228603	snp	C/T	0.00716266	0.059414	intron-variant	LRSAM1	GRCh38.p7	9:127491759	TCTGGGGCTCCAGCC[C/T]GGGAGTCCTGCGCAC	90678
rs148282029	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497398	GTGGGCTCTGGTGGG[A/G]ACAGTCATTTGCTTA	90678
rs148296067	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127487183	AGCAAGACTCTGTCT[-/C]AAAAAAAAAAAAAAA	90678
rs148348874	in-del	-/AT	0.00557542	0.0525036	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503931	ACAATTCTTGGAGCC[-/AT]ATACACTTGCACTCG	90678
rs148528063	snp	C/T	4.95005e-05	0.00497471	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127459017	GGTTCTAGATCTCCA[C/T]GATAATCAGCTGACA	90678
rs148542461	snp	A/G	0.00914312	0.0669923	intron-variant	LRSAM1	GRCh38.p7	9:127464579	GCTACCATTTTAGAC[A/G]ATACAGCTCAGAGCA	90678
rs148597126	snp	C/T	0.021333	0.101051	intron-variant	LRSAM1	GRCh38.p7	9:127499569	ATATGAATGCCCCCT[C/T]GAAATGGTGGTTTGG	90678
rs148667376	snp	G/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127488258	ATATTACTCTGTTTA[G/T]CGTTTTTGTTTTCTT	90678
rs148704769	snp	C/T	0.00177197	0.0297127	intron-variant	LRSAM1	GRCh38.p7	9:127467843	AAGGTAAAGCCAGGC[C/T]GCTGCCTCCTCCCCT	90678
rs148846371	snp	A/C/T	1.65466e-05	0.00287628	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501087	GTGAGGCCATCCGCT[A/C/T]CCCCTGCAGAGCTGG	90678
rs148862951	snp	A/G	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127466172	AAATTAGCCGGGTGT[A/G]GTGGCGCATGCCTAT	90678
rs148930193	snp	A/G	0.00438332	0.0466095	intron-variant	LRSAM1	GRCh38.p7	9:127482738	ATTTTCTAAGGGAGC[A/G]TCCATCTTTTTACAC	90678
rs148986269	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127490602	CTCTCCCTTACCTGC[C/T]CTGTGTCCTTGAGCA	90678
rs149133457	snp	A/G	0.00795532	0.062565	intron-variant	LRSAM1	GRCh38.p7	9:127477774	TTGTGTGGGCCGGGC[A/G]CAGTGGCTCATGCCT	90678
rs149191668	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127457065	AGGATGGCTGCAGGG[A/G]GATCCCTTCTCAGAT	90678
rs149225646	snp	A/G	0.0189856	0.0955633	intron-variant	LRSAM1	GRCh38.p7	9:127463156	GTGAGCCGAGATTGC[A/G]CCATTGCATTCCAGC	90678
rs149250934	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461310	CAGCTCTGGGCCATC[C/T]TGGCCGGGATCCACA	90678
rs149313275	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127501881	TTTGATGATTCCAGG[A/G]TCTCCCGTTGACCTG	90678
rs149397375	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127475606	TCCTCAAGATTGGCA[C/T]ACATTTTGACATGAC	90678
rs149456922	snp	C/T	0.000461848	0.0151892	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479416	AAACTCGAGTTTGAA[C/T]GGCGCCTGGAACTGG	90678
rs149540339	snp	C/G	0.00090676	0.0212734	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485801	ATGGCCTACGAATCT[C/G]AGAGGCAGAACTTGG	90678
rs149713102	snp	C/T	0.00953873	0.0683987	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453975	TGGCTCCATGGAACT[C/T]GCTAGAAAGACACTG	90678
rs149717063	snp	G/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127476809	CCTCCCGAGTAGCTG[G/T]GATTACAGGCACCTG	90678
rs149765084	in-del	-/TTA	0.00795532	0.062565	intron-variant	LRSAM1	GRCh38.p7	9:127475047	AATGCATTTGGGATT[-/TTA]TTATTATTATTATTA	90678
rs149769300	snp	C/T	6.61102e-05	0.00574898	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127457372	CAAATCCTGCAGCCT[C/T]CTGAGTCTGGCAACC	90678
rs149780482	snp	C/T	0.00716266	0.059414	intron-variant	LRSAM1	GRCh38.p7	9:127499141	ACTTTGGGAGGCCTA[C/T]GTGGGAGGATCACTC	90678
rs149893094	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127469922	GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC	90678
rs149944984	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474164	CTGCTGCTGTCTGTT[C/G]CCTGAACTAACCATG	90678
rs149986967	snp	C/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127462892	ATTCAAGCCAGACCT[C/T]AAAGGAGGAATAAGA	90678
rs150050253	snp	A/C/G	0.00438332	0.0466095	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503806	GAGGCAGCTGAGGCT[A/C/G]ATGGGGGTAAATGCT	90678
rs150062009	snp	C/T	0.000421646	0.0145136	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496045	ATCTTTGCGCACCAC[C/T]GCCTCTCACTGGACC	90678
rs150095513	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127501430	ATTTACCCTGCAGAG[A/G]CTTTAGAAAATCATC	90678
rs150191258	snp	A/G	0.0146672	0.084371	intron-variant	LRSAM1	GRCh38.p7	9:127482166	TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTC	90678
rs150211830	snp	C/T	0.0872718	0.189788	intron-variant	LRSAM1	GRCh38.p7	9:127471514	ATTTTGGGCTGGGCG[C/T]GGTGGCTCACGCCTG	90678
rs150253618	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460310	GCCCCCATTGCATCT[A/G]TTTTTAATGGTTAGT	90678
rs150292099	snp	A/G	0.000527113	0.0162259	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462314	CTGCGTACCCTCAAC[A/G]TCAGTGGAAACGAGA	90678
rs150304755	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127464289	CTGGAACTTTCTGCA[A/G]TGATGGAAATGTTCA	90678
rs150344223	snp	A/G	0.000230848	0.0107411	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485775	AGAGCTGTAAGAACC[A/G]GCTCATCCAGATGGC	90678
rs150462961	snp	A/G	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127496552	TTGTAGCACCTGCAC[A/G]TGCGGGGCACCATTT	90678
rs150531352	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127472699	AACCATAAAAGGTAT[C/T]ATATGATGTGATTCT	90678
rs150590236	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492351	TCCCTGCCCACAAGT[A/G]TGGCAGGGCTCTGGC	90678
rs150626916	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127464848	AGGTCCCACTATGTT[C/G]CCCAGCCTGGTCTCA	90678
rs150684800	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127475306	GACCAGCTTGGCCAA[C/T]GTAGTAAAACCCTGT	90678
rs150746934	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452555	GGGCCCTGAATCAAT[A/G]TTGCTTGCATGTGGG	90678
rs150782277	snp	C/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127497681	AGCCCGTCCCCAGGG[C/T]CTGCAGTATACCCAA	90678
rs150784835	snp	A/G	0.000181185	0.00951628	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127455019	GAAGCTGGGGCAGAT[A/G]ACATTCTCGACATCT	90678
rs150820300	snp	C/G	0.000131796	0.00811668	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473901	TGATGGGCCCACGGA[C/G]AGATTCTCAAGGGAG	90678
rs150834683	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127503388	CAACCCTGGGTCTCC[C/T]TCTCTGCTGCTCCCC	90678
rs150882646	snp	A/C	0.000411374	0.0143359	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495982	GAGGGGATGGAGCGC[A/C]AGCTGGTGGCCCTCC	90678
rs150936510	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127481219	TTTGAAATCGCTGGA[A/G]AATGAAAGGTAAGTG	90678
rs150984897	snp	C/T	0.000280393	0.0118371	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502837	TGCTGCCAGCCACTG[C/T]GCACCTGCCCGCTGT	90678
rs151004394	snp	A/G	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127476297	AGATTGCAGAACAGG[A/G]TGGGCTAGTCTATTT	90678
rs151069056	snp	A/G	1.6473e-05	0.00286988	intron-variant	LRSAM1	GRCh38.p7	9:127455079	GGATAGTGTTGGGCT[A/G]TGAATTGGATCTGTC	90678
rs151079638	snp	C/T	0.0103295	0.0711199	intron-variant	LRSAM1	GRCh38.p7	9:127499953	AAACTTTAGTTTTTC[C/T]TGTTATAAAAAATAA	90678
rs151280323	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127488552	CAGGCATCAGACACC[A/G]TGCCCAGCCTGTTTA	90678
rs151323851	snp	A/G	0.000214276	0.0103485	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462259	CTCTGCAGACAACAA[A/G]CTGAAGGAGCTTCCA	90678
rs151329660	snp	A/G	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127495214	CACCTTGGCCCCCCA[A/G]AGTGCTGGGATTACA	90678
rs180994211	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127456116	TTGCAGCTTTGAATG[C/G]AGATGGGTAGAAGCG	90678
rs181001966	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127477475	TACCTGTGTGCCAGG[C/T]GCAGTGGCTCACGCC	90678
rs181016743	snp	A/C	0.00194496	0.0311239	intron-variant	LRSAM1	GRCh38.p7	9:127502751	GGTAGGGCCAGCCAC[A/C]TGCTCCCGCTCTCCC	90678
rs181080776	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472206	ACCTCGTGATCCACC[C/T]GCCTCAGCCTCCCAA	90678
rs181088879	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497088	CACAGCTATGGTGCC[A/G]CACTGCCTCATCCTG	90678
rs181268730	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127483545	CTGCAGTATTAGCAT[C/T]CCATTAGCATGTTAT	90678
rs181317056	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459760	GACTTGTTTTCACCA[C/T]GTTGGCCAGGCTGAC	90678
rs181325702	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127453517	TTGAGCTCCCTGAGG[A/T]CCTGGCTGGCTCTGG	90678
rs181332001	snp	C/T	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127502053	CAGTGGCTGCTGCTC[C/T]GGGTTGGGATTGTTT	90678
rs181335095	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127476293	GGGCAGATTGCAGAA[C/T]AGGATGGGCTAGTCT	90678
rs181350540	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467550	AAGGTAGGGCATCAC[A/C]CTGCCTGCCTACAGT	90678
rs181485998	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489648	GCCCAACAAGAGGTC[A/G]AGGCCTTGCCCTCAG	90678
rs181651395	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461730	ACTTGCTCAAGACCA[C/T]CCCGTGGGATGGTGA	90678
rs181673304	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127485437	TGGCAGGCGTCTGTA[A/G]TCCCAGCTACTCGGG	90678
rs181718451	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127488869	GTGCTGGGATTACAG[A/C]CATGAGCCACCGGCC	90678
rs181865976	snp	C/T	0.00358779	0.0422022	intron-variant	LRSAM1	GRCh38.p7	9:127496837	CATGCCGCTCAGGCT[C/T]TGGAGGCTGAGGGAC	90678
rs181866644	snp	C/T	0.00517822	0.0506191	intron-variant	LRSAM1	GRCh38.p7	9:127467058	TATAGAGAAACACCA[C/T]ACTTTGAGACAAATT	90678
rs181930031	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478596	CTGTAGGTGTGTTAC[A/G]CAGACATCCATGGGC	90678
rs181940501	snp	C/T			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454104	GACGCAGCCCCTGCC[C/T]CCGTGGAACTCACTA	90678
rs182109052	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127471280	GCCCAGGAGTTCAAC[A/G]TGGGCAACATGGCAA	90678
rs182178535	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127463241	GAGCAGACCTGGATA[A/G]CAGGGGCAGCCCAGG	90678
rs182192023	snp	A/G	0.00337979	0.0409692	intron-variant	LRSAM1	GRCh38.p7	9:127461122	GCCTCCCAAAGTGCT[A/G]GGATTACAGGCATAA	90678
rs182217012	snp	C/T	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127456788	GGAGAATTGCTTGAA[C/T]CTGGGAGGCGGAGGT	90678
rs182406489	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127499696	AGCACTTTGGGAAGC[C/T]GAGGCGGGCAGATCA	90678
rs182410554	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473685	CCCAGGCTAGGGAAG[A/G]GGAGAGCAGTGGCTG	90678
rs182429667	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127468139	AAGCAGAAAGCTGTT[C/T]CGCCAGTAGGTGCAT	90678
rs182472260	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127484590	GTCTCAAACTCCTGG[A/G]CTCAAGCAGTCCTCC	90678
rs182733271	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457936	AATGACAAGAGAAAA[G/T]CCTGTATGTGTTCAC	90678
rs182741521	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127490343	TTGCCGGACATGAAG[C/T]TCATTCCTCTGACCA	90678
rs182752700	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127486234	CCAGGATTTGAGCCC[A/G]GCAGAGGGGAGGGGT	90678
rs182801398	snp	A/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485596	ACAAAGGGTTTTTTT[A/T]AAGATAACTATCAGG	90678
rs182807538	snp	C/T	0.00795532	0.062565	intron-variant	LRSAM1	GRCh38.p7	9:127479257	GGCCCTGGAGGGGAG[C/T]GGGGGTTGCTCAGCA	90678
rs183022187	snp	A/G	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127480870	TTTTTGTAGAGATAA[A/G]GTTTCTCCATGTTGA	90678
rs183189376	snp	A/C	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127465008	TGGTGGCACCTCGGA[A/C]AAACCTTCTTTTAGG	90678
rs183198824	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487280	GCTGCTCCTTGCTCC[C/T]TGCCCAGGGTGAGAG	90678
rs183251166	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492198	GTCCTCCAGGCCCAG[A/C]CTGTGCCATCAGGCC	90678
rs183254320	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127468701	TTAATTAAGGCCAGA[C/T]ATGGTGGCTTGCGCC	90678
rs183340967	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127469511	ATACAGATAGCAAAC[A/G]GTATCTGAAAAAATT	90678
rs183486750	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127472436	CCCCTGAGGTCAGGA[A/G]TTCGAGACCACCTTT	90678
rs183578281	snp	C/T	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127466707	TTTTTCACTCACTTA[C/T]GTATTTATCCAAAGT	90678
rs183589974	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450968	TGGGCAGCTCCGAAA[C/T]TCACACCGGGGAGGC	90678
rs183591209	snp	C/T	0.0228947	0.104514	intron-variant	LRSAM1	GRCh38.p7	9:127488498	AACTCCTGACCTCAG[C/T]TGATCCACCCACCTC	90678
rs183596713	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127493439	ATGCGCCTTTTAAAC[A/G]TGGCATGCTGCATAC	90678
rs183622845	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493896	ATGCCCTCTGAGCTG[C/T]GTCCTAGGCCGGGTC	90678
rs183626532	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497807	CAGGTGTGGAGTCTG[A/G]GGTCTGCCATGTGCT	90678
rs183796369	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127469827	AAAATTAGCAAGGCG[C/T]GGTGGCGGGCGCCTG	90678
rs183820865	snp	A/G	0.00636936	0.0560724	intron-variant	LRSAM1	GRCh38.p7	9:127472832	GGCACCTGTAGCTTC[A/G]TAGCCATCCCTGTTG	90678
rs184044725	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454231	AACTCACTGGAAAGT[C/T]GCAGCCTCTGCCCCC	90678
rs184057869	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127502131	AGCCTGAACACCCTG[C/T]GTGCCCTCCGGCAGG	90678
rs184059467	snp	A/G	0.00159617	0.0282053	intron-variant	LRSAM1	GRCh38.p7	9:127476774	CTGCCTCTCAGGTTC[A/G]AGCAATTCTCCTGCC	90678
rs184257921	snp	A/G	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127474244	TCTCCCCACTCACTT[A/G]TCTTATCCTTCAGTT	90678
rs184372885	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460291	GTGTTAGCCACCGTG[C/G]CTGGCCCCCATTGCA	90678
rs184375220	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452720	ACTGAGGCTCTGAGA[A/G]GTGAACCAAGGTGAC	90678
rs184466085	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458661	CATCTATAATTTTAC[A/G]CTGTGGAGTACCACT	90678
rs184483383	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127482938	TGAATGAATGGATGG[A/G]TTTTTTTCTAGAATA	90678
rs184494744	snp	C/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127483731	TACAGTGGTGCGATC[C/T]TGGCTCACTGCAACC	90678
rs184592294	snp	C/T	0.00478085	0.0486577	intron-variant	LRSAM1	GRCh38.p7	9:127494837	GTAGTCCCAGCTACT[C/T]GGGCACTCCAGCCTG	90678
rs184597584	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127470661	TGTTTTATACTCAAT[A/G]TGTGGATACCACACG	90678
rs184631604	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487541	GGCCCACCCAGGGCC[C/T]GGCTCCCAGCAGGTA	90678
rs185181965	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453238	AGGCGCATATCACCA[C/T]GCCCAGCTTCTTTGT	90678
rs185184166	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500580	GTGGAGAAGCCAAGA[A/G]CTGGCCCTTCACTGA	90678
rs185256079	snp	C/T	0.0123036	0.0774623	intron-variant	LRSAM1	GRCh38.p7	9:127496869	GTGGGGCTCGTGTGC[C/T]GCTGCTGCTTAGTGG	90678
rs185290397	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127475270	CCGAGGCTGGTGGAT[C/G]ACTTGAGGCCAGGAG	90678
rs185292776	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127468418	AAAACCCGGAGCCAG[C/T]ACTGGCTGGAGGCGG	90678
rs185301048	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127491601	TGCTGGGTGCGGGCC[C/T]GCCGCTGAGCTCCTG	90678
rs185352597	snp	A/G	0.0138799	0.0821421	intron-variant	LRSAM1	GRCh38.p7	9:127497195	TGTGCCACGTGGCTC[A/G]CACCATTTAGCGGGC	90678
rs185358939	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472251	AGGCGTGAGACACCA[C/T]GCCTGGCCAAGAAAT	90678
rs185427720	snp	C/T	0.00517822	0.0506191	intron-variant	LRSAM1	GRCh38.p7	9:127481711	CACTCCTGAAAAACA[C/T]TCAGAGACATGAATA	90678
rs185832786	snp	C/G	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127462160	GGATCTGTTGTGTGC[C/G]CTAGAGGTCAGAGTG	90678
rs185845333	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127485449	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGAGG	90678
rs185897239	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127489057	AGCTTGTCTGAGGAA[A/G]ATTCTCCATTTCTCA	90678
rs185899552	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467292	TCCAGGTGCAGGGGC[C/T]TAAACTATCACAAAG	90678
rs185911080	snp	A/G	0.00517822	0.0506191	intron-variant	LRSAM1	GRCh38.p7	9:127456798	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	90678
rs185918767	snp	C/T	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127477697	CGCGGCTGCAGTGAG[C/T]TGAGATTGTGCCACT	90678
rs186037205	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456256	TTTTTTTTTGAAGAC[A/G]GACGCTCTGCTCTGT	90678
rs186068665	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	LRSAM1	GRCh38.p7	9:127503903	CCGTGCGGTTGTGCA[A/G]GTTGGTCACTGCACA	90678
rs186139632	snp	A/C/T	1.6501e-05	0.00287232	missense, synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127485812	ATCTCAGAGGCAGAA[A/C/T]TTGGTCCAGCAGGCC	90678
rs186148880	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127461146	GGCATAAGCCACTGC[A/G]CCTGGCTGCCTCTTC	90678
rs186485174	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490018	GGCCCAGGAGGAGGC[A/G]GTCCTCCTCTTAGAC	90678
rs186675387	snp	A/C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127467680	AATTGATAAGGAAAT[A/C/T]GTGTGGTCTCCGGTT	90678
rs186699914	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127471914	GTGATCCACCCACCT[C/T]GGCCTCCCGAAGCGC	90678
rs186712811	snp	A/G			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452459	AGAGCTGCCATCTTT[A/G]CCCATCCCTCTGAGG	90678
rs186724662	snp	A/G	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127499697	GCACTTTGGGAAGCC[A/G]AGGCGGGCAGATCAC	90678
rs186724786	snp	C/G/T	1.64735e-05	0.00286993	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127473842	TCTCAGTACTTGCTG[C/G/T]CAATTCTGGAGCAAG	90678
rs187026210	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478700	GAAGAGCCCCTCCTA[C/T]AGTGCCATGCACACA	90678
rs187117973	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457704	CAAGAAGGAAGAGGA[C/G]GGACGCGCAGGTGAT	90678
rs187146561	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127479644	CCCAGCACCTGGGAG[A/G]GCCCTTACAGATCAC	90678
rs187318905	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127484707	GGAATGTGGGTTGTT[C/T]CCACTTTTTGACTCT	90678
rs187353121	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127497723	AGGCATGCCTGTGGA[A/C]ATGGAGAGATGTCCA	90678
rs187369979	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127487291	CTCCCTGCCCAGGGT[A/G]AGAGTGCCGGGAAGG	90678
rs187433417	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127480871	TTTTGTAGAGATAAG[A/G]TTTCTCCATGTTGAC	90678
rs187576746	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127492962	TTAACAGACTTGCCA[C/T]TTTTAGAAACACCTG	90678
rs187596348	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472724	GATTCTATGCCTTGC[C/T]TTTTTTGTCTCTCAA	90678
rs187596979	snp	A/G	0.00953873	0.0683987	intron-variant	LRSAM1	GRCh38.p7	9:127482633	AGGTGAAAAGATTTT[A/G]CTTTCTTTAGTTACC	90678
rs187644239	snp	A/G	0.0138799	0.0821421	intron-variant	LRSAM1	GRCh38.p7	9:127463148	AGATTGCAGTGAGCC[A/G]AGATTGCGCCATTGC	90678
rs187690497	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127458069	TTCTCCAAGGCCTTT[G/T]TTGTGCATTTTCATT	90678
rs187977837	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127494219	GGGAGGGCCAACGAC[A/G]GAAGGGAGCAGTGGG	90678
rs187985772	snp	A/C	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469921	AGTGAGCCGAGATTG[A/C]GCCACTGCACTCCAG	90678
rs188022366	snp	A/T	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127463592	AGCACACCAGTCACA[A/T]TGGATTAGGGCCCAG	90678
rs188041445	snp	C/T	0.0119091	0.0762411	intron-variant	LRSAM1	GRCh38.p7	9:127486372	CTGGGGTCCGGCTCC[C/T]TGTGCTCACTGGGCA	90678
rs188138435	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493477	GAGCAGCCTGTTTCC[A/G]CACATTCTTTTCAAG	90678
rs188370006	snp	A/G	0.00636936	0.0560724	intron-variant	LRSAM1	GRCh38.p7	9:127472924	TGCACTTTCCCCTAG[A/G]GTGTGTGAGAGGGCA	90678
rs188402590	snp	C/T	0.00517822	0.0506191	intron-variant	LRSAM1	GRCh38.p7	9:127469734	TTTGGGAGGCCGAGG[C/T]GGGCGGATCATGACG	90678
rs188444069	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469197	AAGAGAATATCCACA[C/T]GGTGGCTCACACCTG	90678
rs188464965	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127497973	AGCATGTCCCCCATC[A/T]GGTCCCATTGCTGGC	90678
rs188485077	snp	C/T	0.00438332	0.0466095	intron-variant	LRSAM1	GRCh38.p7	9:127465083	TTCAGGTGTCACGCA[C/T]GCCACCCACCAAACA	90678
rs188584505	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127456015	GGCTTATGAACCCCG[A/G]TGTTAGTAATAATAG	90678
rs188602514	snp	C/T	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127476968	AGGCATGAGCCACCG[C/T]GCCCAGCCAGAATTG	90678
rs188608898	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127502456	TTGGGAGGCCGAGGC[A/G]GGCAGATCACTTGGG	90678
rs188658169	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451136	TAAGGCCCAGAAAGG[C/T]TGAGGCTTGGCCGGG	90678
rs188824575	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127459706	TGGGATTACAGGCAC[A/G]CGCCACCACACCTGG	90678
rs188901640	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127475901	ATGCGCCACCATGCC[C/T]GGCTAATTTTGTATT	90678
rs188905421	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453315	TCGAACTCCTGGGCT[C/T]AAGTGACCCACCTGT	90678
rs188914919	snp	C/T			upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452778	GATTCAAACCCAGTT[C/T]TCTTTTCATCCCAAA	90678
rs188948804	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127500316	CAGTGAGCCGAGATC[A/G]CGCCACTGAACTCCA	90678
rs189016792	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127484070	CTGTCCCTAGTAAAC[A/G]CTAACTCCCCGTGCC	90678
rs189209972	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474382	AAGTGATCCTCCCAC[C/T]TCAGACTCCCAAAGT	90678
rs189270036	snp	A/G	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127466399	GATAGATATCCCTCC[A/G]ATTTTTTTCTATAAA	90678
rs189308149	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127460426	CCCAGCACCACTGCC[A/G]GCCTGAGGCCTTGGG	90678
rs189488293	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127466886	CATGTGCTTATAGTC[C/T]CAGCTACTCAGGAGG	90678
rs189498179	snp	A/C	0.00199481	0.0315187	intron-variant	LRSAM1	GRCh38.p7	9:127488696	ACTCCTGGGCTCAAA[A/C]GATCCTCCCACCTTT	90678
rs189791238	snp	C/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127496893	TTAGTGGCTTGGCCT[C/G]CAAGGCTTCTCTCCT	90678
rs189843482	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127489585	GTGGCCCTCCAGGGC[A/G]GCAGGTCGCAGCAGT	90678
rs190024680	snp	A/G	0.00676609	0.0577691	intron-variant	LRSAM1	GRCh38.p7	9:127472119	GGCGCCCACCACCAC[A/G]CCTGGCTAATTTTTG	90678
rs190058416	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127480251	CCCCAAGCTTCCCAT[C/T]TATAAAGTGAGTGGG	90678
rs190084298	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127501646	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG	90678
rs190101207	snp	C/T	0.0126979	0.078662	intron-variant	LRSAM1	GRCh38.p7	9:127467494	AAAATGGAGTCTGTC[C/T]GGCTCTCTCTCTGCT	90678
rs190107383	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127485562	CTGCATCTCAAAAAA[C/T]AAAACAAAACAAAAA	90678
rs190121619	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127473356	GCACCTACAAATCAA[C/T]AGGAAAAAGACAAAC	90678
rs190295735	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127471250	TTGGGAGGCCAAGGC[G/T]GGTGGATCGCTTGAG	90678
rs190372376	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127456915	AGATGACCTGGACTG[A/G]GCCCTGGCCCCTCTG	90678
rs190382495	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127478755	GGTGTCCACTGGAAC[C/T]ACCTGGTGCCCTTGA	90678
rs190555589	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127496315	ATCCTGGGGAGGTGG[A/G]TCCTGCTGACCTGAT	90678
rs190679806	snp	C/T	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127486156	GCCCGATTTCACAAT[C/T]GCAACTCAGGTTCTG	90678
rs190811122	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127461328	GCCGGGATCCACAGG[C/T]TGCCCCGCCCGGGAG	90678
rs190829661	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127485418	AAAAATTAGGCGGGC[A/G]TGGTGGCAGGCGTCT	90678
rs190919350	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127463190	GACAACAAAGCAAGA[C/T]TTTGTCTCAAAAAAA	90678
rs191039161	snp	G/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127468423	CCGGAGCCAGCACTG[G/T]CTGGAGGCGGGAGGA	90678
rs191050678	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127491809	GGACTGGCAGCTGGC[A/G]TCCTGGACTGGATGC	90678
rs191106111	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127468108	CTGACACGGAGTCAT[A/G]GTTAAGATCTAGAAA	90678
rs191174800	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127452536	TCTCCCTAGCTCCTC[A/T]AGCGGGCCCTGAATC	90678
rs191190900	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127462184	CAGAGTGGCTCCCAG[C/T]GGGCATCAGGCAGGA	90678
rs191212168	snp	A/G	0.00478085	0.0486577	intron-variant	LRSAM1	GRCh38.p7	9:127499283	GGGGGCAAAGGTGGG[A/G]GGATCGCTTGAGCTT	90678
rs191362421	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127457838	GCTTGGGAGAGTGAT[A/G]TGCACCTTCAGAGGA	90678
rs191370719	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127490294	TTTGGACCAATTTAC[C/G]TTTTTAATTTCCCTC	90678
rs191390682	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127474077	GAACTGGCCTCCTGA[C/T]GAGTTGAACTGCTTT	90678
rs191399506	snp	A/G	0.0103295	0.0711199	intron-variant	LRSAM1	GRCh38.p7	9:127499933	CATCTCAAAAAAAAA[A/G]AGAAAAACTTTAGTT	90678
rs191648450	snp	C/T	0.0107246	0.0724382	intron-variant	LRSAM1	GRCh38.p7	9:127469790	AACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT	90678
rs191699919	snp	A/G	0.00020621	0.010152	utr-variant-5-prime, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451327	CGGCATGGTGGAGGC[A/G]GCTGGTGTCGGATGA	90678
rs191915695	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127472781	CATAGTACGGTTTGA[A/G]TGTCCCCTTAAACTG	90678
rs192132096	snp	C/T	0.00874735	0.0655527	intron-variant	LRSAM1	GRCh38.p7	9:127456670	GAGATCAAGACCATC[C/T]TGGCTACCATGGTGA	90678
rs192211099	snp	A/T	0.0192403	0.0961766	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450813	AGGTATACTGGGGGA[A/T]AAGAAGAGTTAGTGT	90678
rs192249276	snp	A/G	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127497785	TGAGGCCCGTGGGGA[A/G]AAGGGGCAGGTGTGG	90678
rs192265012	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127458628	AAATTAGCAAGTACA[A/G]TTAAGCAAAGGGGGA	90678
rs192282483	snp	G/T	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127482813	GGTTGCTTGTGATGC[G/T]GTAGGCATCCAGAGA	90678
rs192455421	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127487948	GGGGGGCCCGGGGGA[A/T]GGTCTTCTGGTCACT	90678
rs192481020	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127463974	CTGACAGCAGAGATC[A/G]TTGTAAACCAGGCCG	90678
rs192498944	snp	G/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127486625	ACACTGTGCTTAGGA[G/T]TTGCAAGCGCAGGGG	90678
rs192507003	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127477868	GCTTGGCCAATATGG[C/T]GAAACCCTGTCTCTA	90678
rs192554248	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127494236	AAGGGAGCAGTGGGC[A/G]TGGCCAGGTCCAGGA	90678
rs192558887	snp	C/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127469958	ATACAGAGCAAGACT[C/G]CATCTCAAAAAAATA	90678
rs192731915	snp	A/G	0.00279162	0.0372561	intron-variant	LRSAM1	GRCh38.p7	9:127465530	GTTCATTTGCTTCCA[A/G]GTATGGGGTTTTCTG	90678
rs192772527	snp	A/G	0.0142736	0.0832652	intron-variant	LRSAM1	GRCh38.p7	9:127466567	TATGTTGCCCAGGCT[A/G]GTCTCGAACTCCTGG	90678
rs192906020	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493491	CGCACATTCTTTTCA[A/G]GTCATTAAACTATTC	90678
rs192933247	snp	A/G	0.00318978	0.0398085	intron-variant	LRSAM1	GRCh38.p7	9:127487300	CAGGGTGAGAGTGCC[A/G]GGAAGGACAGCTTTG	90678
rs192956305	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127493201	CGAGTAGCTGGGACT[A/G]CAGGCATGTGCCACC	90678
rs193059105	snp	C/G	0.00835141	0.0640778	intron-variant	LRSAM1	GRCh38.p7	9:127469356	GCACCTGTAATCCCA[C/G]CTACTCAGGAGGCTG	90678
rs193089410	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127474709	GTCTGGGACACACAC[C/T]CACCATGCTCTGGGT	90678
rs193107843	snp	A/T	0.0314385	0.121371	intron-variant	LRSAM1	GRCh38.p7	9:127458205	GGCCAACATGGTGAA[A/T]CCCCGTCTCTACTAA	90678
rs193249748	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RPL12, LRSAM1	GRCh38.p7	9:127453083	TCACTTTATTTATTT[A/G]TTTATTATTATTTTC	90678
rs193253392	snp	A/T	0.000798403	0.0199641	intron-variant	LRSAM1	GRCh38.p7	9:127500543	GATGGGCAGCAGCCC[A/T]TCCTGTCTCCTGGGC	90678
rs193260468	snp	A/G	0.00119737	0.0244387	intron-variant	LRSAM1	GRCh38.p7	9:127480953	CAAAGTGCTGGGATT[A/G]CAGATGTGAGCCACT	90678
rs199558213	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127458598	TAAAACAAAATAAAA[-/T]TAAAATTAAATTAAA	90678
rs199623837	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127502711	AAAAAAAAAAAAAAA[C/T]ACGGGCCTGGGACTC	90678
rs199636274	snp	A/G/T	1.7029e-05	0.00291791	intron-variant	LRSAM1	GRCh38.p7	9:127481249	GTTCTTCCAGGGGAG[A/G/T]GCAGCATTTTTTTTT	90678
rs199681048	in-del	-/A	0.0252325	0.109451	intron-variant	LRSAM1	GRCh38.p7	9:127455247	TATAACGTAGTCTCC[-/A]AAGAGTCAAGGAGTC	90678
rs199703262	snp	A/C/G	3.39768e-05	0.00412158	synonymous-codon, missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492816	GGAGATGATCTCGGA[A/C/G]CAGCGCTGGGCCCTC	90678
rs199754114	snp	C/T			intron-variant, upstream-variant-2KB	RPL12, LRSAM1, SNORA65	GRCh38.p7	9:127449603	GAAACCAAGCACAAG[C/T]AAATACCTGGGCCTG	90678
rs199887448	snp	A/G	0.000247879	0.01113	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501047	GGTCGTCACCCCTAC[A/G]GCCCCCCAGGAGCCT	90678
rs199916476	snp	C/T	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127467857	CCGCTGCCTCCTCCC[C/T]TCATTGAGGAACTAT	90678
rs199925705	snp	C/G/T	0.000115525	0.00759936	intron-variant	LRSAM1	GRCh38.p7	9:127458994	CTCACAGGGGTCTTT[C/G/T]TTCTGCAGGTTCTAG	90678
rs199932024	snp	A/G	0.000222845	0.0105533	intron-variant	LRSAM1	GRCh38.p7	9:127496115	GCAGCAGCCGTCTGC[A/G]TGGAGGGGAGGGGCA	90678
rs199947399	snp	A/G	1.65127e-05	0.00287334	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479442	ACTGGGGCAGCGGGA[A/G]CACACCCAGCTCCTT	90678
rs199997686	snp	A/G	0.000187433	0.00967893	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496011	CCTGGAGGAGCTGTC[A/G]GCTGAGCACTACCTG	90678
rs200004729	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127467163	GTTTTGTTTTTATAC[C/T]GTGGTCTAAATAGGG	90678
rs200029126	in-del	-/T	0.00953873	0.0683987	intron-variant	LRSAM1	GRCh38.p7	9:127459455	ACTCCTGACCTCAAG[-/T]TTATCCACTCACTTT	90678
rs200041999	snp	A/T	0.000330278	0.0128464	intron-variant	LRSAM1	GRCh38.p7	9:127458970	CTGAGGGACTTTCTC[A/T]CTTGGAGACTCACAG	90678
rs200075998	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127457968	ACAGATGCTTTCTTT[C/T]TTTTTTTTTTTTTTA	90678
rs200112922	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127478135	TAATAAATTAATTAA[A/T]TAAACACCAATAATT	90678
rs200115008	snp	A/G	0.00199792	0.0315431	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462294	CCGTGGGGGAGCTTC[A/G]AAGCCTGCGTACCCT	90678
rs200130803	snp	A/T	2.8833e-05	0.0037968	intron-variant	LRSAM1	GRCh38.p7	9:127489438	GGCTGGTGGTCTGTG[A/T]TGCAGAGCGCGATGC	90678
rs200172427	snp	A/G	0.00438332	0.0466095	intron-variant	LRSAM1	GRCh38.p7	9:127466166	ATACAAAAATTAGCC[A/G]GGTGTGGTGGCGCAT	90678
rs200191027	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127458416	AACAAAACAAAACAA[-/C]AACAAAAAAAAACAC	90678
rs200195985	snp	A/C/G/T	0.000204691	0.0101148	intron-variant	LRSAM1	GRCh38.p7	9:127492781	AGCTCACGGTGGTGC[A/C/G/T]GGGTGTGGTCTTGTT	90678
rs200242834	in-del	-/C	0.00953873	0.0683987	utr-variant-3-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502999	GACTCGTATGAGGCT[-/C]CCCCCTGCCCTGGGC	90678
rs200259701	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127462241	GAGCTGTGCTATTGG[A/G]GTCTCTGCAGACAAC	90678
rs200356981	snp	A/C	6.59087e-05	0.00574021	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462306	TTCGAAGCCTGCGTA[A/C]CCTCAACATCAGTGG	90678
rs200391831	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127475749	TTTATTATTTTTTTA[-/T]TTTTTTTTTGAGATG	90678
rs200426609	snp	C/T	0.00199808	0.0315444	intron-variant	LRSAM1	GRCh38.p7	9:127473946	GGTAAGACAAGGCAG[C/T]CTGCTGCACGCATAC	90678
rs200527839	snp	C/T	0.000331912	0.0128781	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479889	CCAGCGCCACCTCAA[C/T]GCAGAGCGGCAGCGG	90678
rs200538913	snp	A/G	0.000209358	0.0102291	intron-variant	LRSAM1	GRCh38.p7	9:127495940	TCTTCCTTCCTGCTC[A/G]TGGTACACGTTTCTG	90678
rs200559623	in-del	-/ATATATA			intron-variant	LRSAM1	GRCh38.p7	9:127466498	TATATATATATATAT[-/ATATATA]TTTTTTTTTTTTTTT	90678
rs200595164	snp	A/G	0.000232891	0.0107885	LRSAM1	9	allele_origin=G(unknown)/A(germline)	9:127481185	ATTTTCTCCACAGAC[A/G]AAAGAAAAGCTCCGA	90678
rs200731968	snp	C/G/T	0.000256684	0.0113263	intron-variant	LRSAM1	GRCh38.p7	9:127457441	CTGCATGGGGTTCCA[C/G/T]GCGGCAGCTGAGCGC	90678
rs200817114	in-del	-/T			intron-variant	LRSAM1	GRCh38.p7	9:127484803	ATTTTTTGATTTTTC[-/T]TTTTTTCTTTTTTTT	90678
rs200873425	in-del	-/G			intron-variant	LRSAM1	GRCh38.p7	9:127491006	AACAAGCACGTCCAT[-/G]GCCCCAGGAACGCGA	90678
rs200877137	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127458419	CAAAACAAAACAAAA[-/C]AAAAAAAAACACCAG	90678
rs200961616	snp	C/T	1.67747e-05	0.00289605	intron-variant	LRSAM1	GRCh38.p7	9:127457272	AGCCTGCCCTGCCTG[C/T]TGCTCTTCCTCAGCC	90678
rs200963472	snp	A/G	7.0995e-05	0.00595755	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487696	CCGAAATGGATGAAC[A/G]ATTCCAGCAGATTCT	90678
rs201068068	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467219	TTTTACAGAAGCAGA[A/G]CTGGCAAAAAGTTAA	90678
rs201137230	snp	C/G	0.00199793	0.0315432	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496067	CACTGGACCTGCTGA[C/G]CCAAATGAGCCCAGG	90678
rs201147184	snp	C/T	1.72469e-05	0.00293652	intron-variant	LRSAM1	GRCh38.p7	9:127479807	CGTCTGAGGGGGTCC[C/T]AGGGGCTCAGGACCC	90678
rs201167958	snp	C/G/T	6.62135e-05	0.00575352	intron-variant	LRSAM1	GRCh38.p7	9:127480020	CCCAGAGTCCTTCCC[C/G/T]GTGCAGTCCCCTGAG	90678
rs201264884	snp	A/G	2.42527e-05	0.00348221	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489480	TTCGAGGCACTCCAG[A/G]TGAAGAAAGACCTGA	90678
rs201279002	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478923	TGACCACTGTCTTTT[C/T]TTCCTCCCAGAACAG	90678
rs201284198	snp	A/G/T	0.00013226	0.00813114	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127501027	CTGAAACCACCAATG[A/G/T]GTGAGGTCGTCACCC	90678
rs201316223	snp	A/G	0.00199792	0.0315431	intron-variant	LRSAM1	GRCh38.p7	9:127479334	CGACTTCTGTGTCCT[A/G]ACTCCCCCAGGGCCT	90678
rs201324048	in-del	-/CG			intron-variant	LRSAM1	GRCh38.p7	9:127479093	TGCCTTCCTCTTACA[-/CG]CGCAGTCTGCTGCAT	90678
rs201329646	snp	A/G	8.37458e-05	0.00647038	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479849	TGCAGGAGCAGTCCC[A/G]GCTGGAGCAGGGCCT	90678
rs201377708	in-del	-/CTTT			intron-variant	LRSAM1	GRCh38.p7	9:127490277	TTTCTTTCTTTCTTT[-/CTTT]TTTTGGACCAATTTA	90678
rs201465928	in-del	-/C			intron-variant	LRSAM1	GRCh38.p7	9:127484810	GATTTTTCTTTTTTT[-/C]TTTTTTTTTTTTTTT	90678
rs201473713	snp	C/T	0.00299558	0.0385852	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454540	AGGATGCCGCTCTTC[C/T]TCCGGAAGCGGAAAC	90678
rs201488957	snp	A/G	9.39232e-05	0.00685221	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127467784	CTACCCGCCGCGGGA[A/G]GTGTGTGGTGCCGGC	90678
rs201509713	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127467454	CTTAAGGGAGGGAGG[G/T]AAGGGGGCTGCAGGT	90678
rs201588177	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127492885	GCGAGAGGAAGAGCT[C/T]CGGGAAATCCTGGTA	90678
rs201671353	snp	C/G/T	1.68227e-05	0.00290018	intron-variant	LRSAM1	GRCh38.p7	9:127497347	CAGGTACAAGCACAG[C/G/T]TCCAGCCTCTTCCAG	90678
rs201673781	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127478071	AAAAAAAAAAAAAAA[C/T]AAGAACCTAACTCTT	90678
rs201702419	snp	C/T	0.000330409	0.0128489	intron-variant	LRSAM1	GRCh38.p7	9:127495948	CCTGCTCATGGTACA[C/T]GTTTCTGTCTTGCAG	90678
rs201714333	snp	A/G	0.000255352	0.0112965	synonymous-codon, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127451300	TTTGATCTCGTTGGG[A/G]TCGAACTTCGGCGGC	90678
rs201731540	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127456234	CTGGAAGTTTTGTTT[G/T]TTTTTTTTTTTTTTT	90678
rs201760862	snp	C/T	0.00110492	0.0234784	intron-variant	LRSAM1	GRCh38.p7	9:127473975	ACATGTGTGTGTGTG[C/T]GTGTGCATGTATGTG	90678
rs201772539	snp	C/T	0.000592895	0.0172074	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127461201	AAAGGAATCAACTGA[C/T]GCAGCTCCCACGTTC	90678
rs201785643	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127491008	ACAAGCACGTCCATG[A/C]CCCAGGAACGCGAGG	90678
rs201800688	in-del	-/TC			intron-variant	LRSAM1	GRCh38.p7	9:127484807	TTGATTTTTCTTTTT[-/TC]TTCTTTTTTTTTTTT	90678
rs201808404	snp	A/G/T	0.000560792	0.0167358	intron-variant	LRSAM1	GRCh38.p7	9:127461272	GGTAGGGACCAAGAA[A/G/T]CCGTGTCCGTGTGAC	90678
rs201822253	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127495717	GGGACAGAGAGGCAG[A/C]TGAAACAGCCCCCTC	90678
rs201896118	in-del	-/ATATATATA			intron-variant	LRSAM1	GRCh38.p7	9:127466496	TATATATATATATAT[-/ATATATATA]TTTTTTTTTTTTTTT	90678
rs201903568	snp	A/G	0.000399281	0.0141238	intron-variant	LRSAM1	GRCh38.p7	9:127481250	TTCTTCCAGGGGAGG[A/G]CAGCATTTTTTTTTT	90678
rs202039008	snp	C/T	9.94085e-05	0.00704942	intron-variant	LRSAM1	GRCh38.p7	9:127485704	CAGGAGCAGCCACTC[C/T]ACTCAGCTGTCCCCA	90678
rs202146452	snp	A/G/T	0.000181578	0.0095267	intron-variant	LRSAM1	GRCh38.p7	9:127458986	CTTGGAGACTCACAG[A/G/T]GGTCTTTCTTCTGCA	90678
rs202166023	snp	A/C/G	0.000550507	0.0165829	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127489447	TCTGTGTTGCAGAGC[A/C/G]CGATGCAGAAGGCTG	90678
rs202170304	in-del	-/AAGAA			intron-variant	LRSAM1	GRCh38.p7	9:127500843	AGGCTCAGAGAAGAG[-/AAGAA]GAGAGTGTGTGGCAA	90678
rs202170746	snp	A/G	3.29859e-05	0.00406102	intron-variant	LRSAM1	GRCh38.p7	9:127479366	TGCTGACAGTCACCA[A/G]GATCTGTGTCTTGCA	90678
rs202216046	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127467269	AGCAGTTACAAAAAA[A/T]AAACAGTTCCAGGTG	90678
rs367563135	snp	A/G			intron-variant, utr-variant-5-prime	LRSAM1	GRCh38.p7	9:127454072	GCAGCCCCTGCCCCC[A/G]TGGAACTCACTAGAA	90678
rs367599324	snp	G/T	0.00016509	0.00908393	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479961	CCGGATCCAGAAGCT[G/T]CTGCAGGACAATCAG	90678
rs367602680	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127500934	ACCATGGGGATGGGC[A/G]GGGCCACAATGAGCC	90678
rs367675534	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127462078	AAAGTCTCTTGGCTA[A/G]TAATTGGTGGAGTGG	90678
rs367795632	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127476028	TACAGGTGTGAGCCA[C/T]CACACCCGCCAGATG	90678
rs367802505	snp	A/G	0.000437904	0.0147905	intron-variant	LRSAM1	GRCh38.p7	9:127458950	AGCGCTCTGGAGCCC[A/G]GAGTCTGAGGGACTT	90678
rs367823841	snp	C/G	0.000510578	0.0159696	intron-variant	LRSAM1	GRCh38.p7	9:127478926	CCACTGTCTTTTTTT[C/G]CTCCCAGAACAGGTT	90678
rs367844312	snp	C/G	0.000273762	0.0116964	intron-variant	LRSAM1	GRCh38.p7	9:127457409	GTACTGGGCCCTCCT[C/G]CCAGGCAGCTGGGGC	90678
rs367847130	snp	A/G	0.000127041	0.00796895	intron-variant	LRSAM1	GRCh38.p7	9:127489420	GGCACGGCCCCTGCT[A/G]AGGGCTGGTGGTCTG	90678
rs367860563	snp	A/G	7.0141e-05	0.00592162	intron-variant	LRSAM1	GRCh38.p7	9:127502759	CAGCCACATGCTCCC[A/G]CTCTCCCTCCCCAGG	90678
rs367882167	snp	A/G	0.000749561	0.0193447	intron-variant	LRSAM1	GRCh38.p7	9:127495288	TTTTATTACCATTTT[A/G]TGACTAACATTGCCT	90678
rs367955076	snp	G/T	0.000461186	0.0151783	intron-variant	LRSAM1	GRCh38.p7	9:127462400	GCTGTTCTTGCCTGG[G/T]GTGCTCTCTGGCCTG	90678
rs367996197	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127455923	TCCTTCCTGAGGTAT[C/T]GTGAGAATTAAATGA	90678
rs368025835	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127492325	GTCATCATGCCTGGC[A/G]GGTGCCCTAGTCCCT	90678
rs368056307	snp	C/G/T	0.00557542	0.0525036	intron-variant	LRSAM1	GRCh38.p7	9:127461473	TCCTGAGAGCCAGGG[C/G/T]CGTATGGCCGTATGG	90678
rs368060643	in-del	-/A			intron-variant	LRSAM1	GRCh38.p7	9:127478052	GCAAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	90678
rs368065377	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127499737	AGATGGAGACCATCC[C/T]GGCTAACATGGTGAA	90678
rs368079086	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127495119	GCCATGCCTGGCTAG[C/T]TTTGTATTTTTAGTA	90678
rs368087217	snp	A/G	1.65214e-05	0.0028741	synonymous-codon, intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495379	GCTGATTCAGTATCA[A/G]CGGCTTTTGAACCAG	90678
rs368088593	snp	A/C/G	4.94958e-05	0.00497452	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479420	TCGAGTTTGAACGGC[A/C/G]CCTGGAACTGGGGCA	90678
rs368138117	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127476642	ATTTGATGATGAAGT[A/G]GCATGAGCGAATTTT	90678
rs368185087	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127467161	TAGTTTTGTTTTTAT[A/T]CTGTGGTCTAAATAG	90678
rs368199689	snp	A/G	3.46681e-05	0.00416327	intron-variant	LRSAM1	GRCh38.p7	9:127496132	GGAGGGGAGGGGCAC[A/G]CAAGGCCGCTGTCCT	90678
rs368202093	snp	C/T	0.000117079	0.00765021	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127502879	ATCGCCCAGCGCCTC[C/T]GCATCTACCACAGCA	90678
rs368203483	snp	C/T	0.00283286	0.0375287	intron-variant, upstream-variant-2KB	RPL12, LRSAM1	GRCh38.p7	9:127450823	GGGGAAAAGAAGAGT[C/T]AGTGTCTGTGCAGAG	90678
rs368243544	snp	A/G	8.19034e-05	0.00639883	intron-variant	LRSAM1	GRCh38.p7	9:127467865	TCCTCCCCTCATTGA[A/G]GAACTATGACCCCCA	90678
rs368327212	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127487400	CAGGCATCCACTTCC[A/G]GGGGGTGCTGGGGAG	90678
rs368333698	snp	A/C			intron-variant	LRSAM1	GRCh38.p7	9:127500358	AGAGCGAGACTGTCT[A/C]AAAAAAAAAAAAAAA	90678
rs368413143	snp	G/T			intron-variant	LRSAM1	GRCh38.p7	9:127470263	CAGTTTCACATGGCC[G/T]GGAGGCCTCAGGAAA	90678
rs368445640	snp	A/G			intron-variant	LRSAM1	GRCh38.p7	9:127467563	ACACTGCCTGCCTAC[A/G]GTCATCCCAGGCACT	90678
rs368471851	snp	G/T	1.74357e-05	0.00295255	intron-variant	LRSAM1	GRCh38.p7	9:127492914	TATGTGTTTGGCTTC[G/T]GTGCTCAGCATCACA	90678
rs368491511	snp	A/G			missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127495970	GTCTTGCAGGAAGAG[A/G]GGATGGAGCGCCAGC	90678
rs368507132	snp	C/T	8.94554e-05	0.00668728	intron-variant, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127487638	TAGGTGCTCGGGAAA[C/T]GTTCCAAGAATGAAT	90678
rs368570954	snp	A/G	7.84683e-05	0.00626323	intron-variant	LRSAM1	GRCh38.p7	9:127487768	TCCTGCAGGAGGTGA[A/G]CCCTCGCCCAGAGCC	90678
rs368602356	snp	A/T			intron-variant	LRSAM1	GRCh38.p7	9:127481794	GGCGCAGTGGCTCAC[A/T]TCTGTAATCCCAGCA	90678
rs368646898	snp	A/G	0.000134194	0.00819019	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127454571	CCAGTGAGGAGGCTC[A/G]GAAACGCCTGGAGTA	90678
rs368674859	snp	A/G	0.000132479	0.00813768	synonymous-codon, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127479928	GCAGCTGAAGCAGAC[A/G]GAACAGAACATTTCC	90678
rs368689811	snp	A/G	1.64779e-05	0.00287031	missense, utr-variant-5-prime, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127462303	AGCTTCGAAGCCTGC[A/G]TACCCTCAACATCAG	90678
rs368722023	snp	C/G			intron-variant	LRSAM1	GRCh38.p7	9:127500900	GAGAGCAGAGGCTCC[C/G]CCACCCTCCAGCTCA	90678
rs368738356	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127465266	TGCTCCTGCTGCCCA[C/T]GATGAGAATGCTCTA	90678
rs368762426	snp	C/T			intron-variant	LRSAM1	GRCh38.p7	9:127500678	CCCGTCTCTGAGCCT[C/T]AAATGTCTCATCTCT	90678
rs368796469	snp	C/T	8.4081e-05	0.00648332	intron-variant	LRSAM1	GRCh38.p7	9:127479516	AGGAGGTTTGTGAGC[C/T]GCCTGCTAGGGTCCA	90678
rs368811991	snp	G/T	0.0023933	0.0345097	intron-variant	LRSAM1	GRCh38.p7	9:127470891	CTCGGCCCAAAGGCA[G/T]TGAGTTATCTCAATT	90678
rs368858589	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	LRSAM1	GRCh38.p7	9:127496082	GCCAAATGAGCCCAG[A/G]GGACCTGGCCAAGGT	90678

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