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

CORO2B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs75734120	snp	C/T	0.081446	0.184634	intron-variant	CORO2B	GRCh38.p7	15:68685837	TGGGCATTGGGATTA[C/T]TTAAACTCCCAGGTG	10391
rs75798891	snp	G/T	0.0165278	0.0893908	intron-variant	CORO2B	GRCh38.p7	15:68638931	CTGTCAACAGCAAGG[G/T]ACTCACTAGGCCTCA	10391
rs75806310	snp	C/T	0.0532157	0.154195	intron-variant	CORO2B	GRCh38.p7	15:68706204	TTCCCTACCTGCTGG[C/T]GCCCGACCCCACACA	10391
rs75813605	snp	A/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68597638	CCATCAAAAAAAAAA[A/T]AATAAATAAATAAAA	10391
rs75866003	snp	C/G	0.0532157	0.154195	intron-variant	CORO2B	GRCh38.p7	15:68706385	GTGCCCCCACAGGCT[C/G]TCCGTCTGCATGCAC	10391
rs76023722	snp	G/T	0.0364509	0.129988	intron-variant	CORO2B	GRCh38.p7	15:68717531	ATGGAGGGGTGGAGA[G/T]GAAAGAAGCAGGAAG	10391
rs76070395	snp	A/G	0.0539704	0.155153	intron-variant	CORO2B	GRCh38.p7	15:68570434	TAGAATGAGTTAGGG[A/G]CTACTGTGGATCTTG	10391
rs76072851	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640950	TGCAGACTCCCAGCT[C/T]AGGGTTCTGTGTGAA	10391
rs76075646	snp	A/C	0.0513262	0.151752	intron-variant	CORO2B	GRCh38.p7	15:68606339	CCTGGAGATCCCTCC[A/C]GGCCAGTGAATCATG	10391
rs76142516	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68709715	TAAAGTGTCCTAAAT[G/T]ATAGTCACATGTGCT	10391
rs76169793	snp	A/G	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68658265	CAGGGAGAGGGAACA[A/G]CTGGGGCCAGGCTGG	10391
rs76170781	snp	A/G	0.0225045	0.103662	intron-variant	CORO2B	GRCh38.p7	15:68687209	CCAGAGAGGCCAGGG[A/G]TTATGTTCAAGGTCA	10391
rs76206045	snp	A/C	0.0383715	0.133092	intron-variant	CORO2B	GRCh38.p7	15:68686669	TTTGGGAGGTTGAGG[A/C]GGGTGGATCACCTGA	10391
rs76229721	snp	C/T	0.0166325	0.0896639	intron-variant	CORO2B	GRCh38.p7	15:68662832	TTTGATAAATTTCAG[C/T]TTCTTATAATAGATT	10391
rs76252057	snp	G/T	0.0103295	0.0711199	intron-variant	CORO2B	GRCh38.p7	15:68671262	AATTTTTCTGTTGTT[G/T]TTTTTTTTTCCTACT	10391
rs76275353	snp	C/T	0.0134861	0.0810011	intron-variant	CORO2B	GRCh38.p7	15:68587754	AAGTCTGTGCTATTA[C/T]TATCCCCCTTTCTAT	10391
rs76275896	snp	A/G	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68716473	TACCAGACCCTGCGC[A/G]AAGTCCAGTGGCAAA	10391
rs76282267	snp	C/G	0.0080288	0.0628485	intron-variant	CORO2B	GRCh38.p7	15:68645129	TGGCACAGGGCCCAG[C/G]CTGACCCTTGTCTCT	10391
rs76341537	snp	G/T	0.039522	0.134904	intron-variant	CORO2B	GRCh38.p7	15:68617068	GAAGCAGGGCTCTGA[G/T]GGGTCAAAAAAATGG	10391
rs76389552	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68690650	ACGTTAGCTTTCTTT[C/T]TTTTTTTTTTTTTTT	10391
rs76396141	snp	C/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68599179	GAAAAGTCTGATTCC[C/T]GCTTTCAAAGCCCAA	10391
rs76398496	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68676005	ATAGAATAATGCTAG[A/G]AGGAGAAATTGATTA	10391
rs76406215	snp	A/G	0.0429648	0.14013	intron-variant	CORO2B	GRCh38.p7	15:68575873	TAAAATGCATGTATT[A/G]GCTGGGTGTGGTGGC	10391
rs76417804	snp	A/T	0.199564	0.24486	intron-variant	CORO2B	GRCh38.p7	15:68560471	AGCTAATTAAAGACA[A/T]TTTTTTTTGTAGAAA	10391
rs76420022	snp	C/T	0.0818113	0.184966	intron-variant	CORO2B	GRCh38.p7	15:68681586	TAAAATTGGGTCTGT[C/T]ACACTTGAGAAGTGT	10391
rs76423893	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612666	AGTTCACACCTTGGT[C/G]TGCTGATGATAACTT	10391
rs76462323	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68562852	CGTGGTGGCAGGCGC[C/T]GGTAGAACCAGCTAC	10391
rs76488704	in-del	-/TTT			intron-variant	CORO2B	GRCh38.p7	15:68605708	TCACAGAGGGCTCTT[-/TTT]GGGTTTTTTTTTTTT	10391
rs76531448	snp	A/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68667030	GCAAAGAAGACCCTC[A/G]ACAAACAGGCCCTAG	10391
rs76546263	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68586179	ATAATAGTAACAATC[C/T]TTTACTATTAAGGAT	10391
rs76561217	snp	G/T	0.0383715	0.133092	intron-variant	CORO2B	GRCh38.p7	15:68674936	TTTGAGAGCAGCAAG[G/T]TGGAGCACGAAAGGA	10391
rs76584330	snp	A/G	0.021333	0.101051	intron-variant	CORO2B	GRCh38.p7	15:68682272	AATTATAGAAAGCCA[A/G]TCTTGCTCTGGAGTT	10391
rs76597028	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68703199	CTCTGTCACCAGGCT[C/G]TCATGCAGTGGCGCG	10391
rs76598365	snp	C/T	0.0513262	0.151752	intron-variant	CORO2B	GRCh38.p7	15:68568116	GGCCACCCCCTGGGG[C/T]TCCTTGTAGGGTCAA	10391
rs76603133	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68596539	GAAAGGAGATTGAAG[A/G]GGAAGGTGGGTTCTG	10391
rs76624645	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588633	CCGATGCCCCCAGCG[C/T]TCAGACCTGCTTTTC	10391
rs76688712	snp	A/G	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68711447	CAGGCCCTGCATGGG[A/G]CGCTTCTCCCAGGGC	10391
rs76727292	snp	C/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68716201	TCCCCACCTCCTTCA[C/G]TGTCACTCCTGCATC	10391
rs76739105	snp	A/G	0.0142736	0.0832652	intron-variant	CORO2B	GRCh38.p7	15:68572581	TGGGGCAGAAGGGGT[A/G]TCAGAATACCTCCTT	10391
rs76776184	snp	A/G	0.0256215	0.110247	intron-variant	CORO2B	GRCh38.p7	15:68668513	CCGAAGGACCTCTCT[A/G]CAAACTTGAATGGGA	10391
rs76781197	snp	C/T	0.0168055	0.0901129	intron-variant	CORO2B	GRCh38.p7	15:68647048	GCTCCACTTTAGGCT[C/T]ACAAGGGTCAACAAG	10391
rs76832297	snp	A/C	0.0626037	0.165477	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726036	CTCATCCCTTAACTT[A/C]TCCCTTACCAGTGAC	10391
rs76863230	snp	A/G	0.0352966	0.128072	intron-variant	CORO2B	GRCh38.p7	15:68655976	ATCTCCCTGGGGGCA[A/G]TTGGGGCCCAGAGGC	10391
rs76867533	snp	C/T	0.0178098	0.0926698	intron-variant	CORO2B	GRCh38.p7	15:68611543	TTTTTTATCTCTGTT[C/T]GGATATATCTTCAAC	10391
rs76876772	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68670059	AAGACTCTGTCTCAG[A/G]AAAAAAAAAGGGGGG	10391
rs76897739	snp	A/C	0.0225045	0.103662	intron-variant	CORO2B	GRCh38.p7	15:68670325	GACTTCAGGTGTGCA[A/C]CACTAAGCCTGGTTA	10391
rs76936954	snp	G/T	0.0193772	0.0965046	intron-variant	CORO2B	GRCh38.p7	15:68656562	ATCCTGGCAGCAAAT[G/T]CTTCAGAACCATCCC	10391
rs76949555	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68617672	CTTTTGGGTGGGCAA[C/T]GCTGGCATCATCACT	10391
rs77008273	snp	G/T	0.0111196	0.0737302	intron-variant	CORO2B	GRCh38.p7	15:68616908	TTTGGAAGACATGCC[G/T]GAGGATAAAACAAAG	10391
rs77012792	snp	C/G	0.077417	0.180873	intron-variant	CORO2B	GRCh38.p7	15:68685543	GCTCACCCTCCCCAA[C/G]ATGAGACAAGACCAA	10391
rs77017896	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68696263	TCAAAAAAAAAAAAA[-/AA]GAGTTCGAGCATGGT	10391
rs77024618	snp	A/C/G	0.0190027	0.0957379	intron-variant	CORO2B	GRCh38.p7	15:68569334	ACCACTGATCTTTTC[A/C/G]CTGTCTCCATAGTTC	10391
rs77042678	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68589523	GATGTACAGTAGAAA[C/T]GCCCATTTTGCAGAG	10391
rs77091661	snp	C/G	0.0337553	0.125452	intron-variant	CORO2B	GRCh38.p7	15:68669517	CGTGAATGCATGAGT[C/G]GGCCAGGGCTAGGAC	10391
rs77092079	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68638075	TGAATACTTTTTCCT[C/T]CCGGGCCCTCCCCAT	10391
rs77098750	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68658319	GGAGGAGGGCGAGAT[A/G]CATGGTGCTCTCCAA	10391
rs77122455	snp	C/G	0.0197687	0.0974348	intron-variant	CORO2B	GRCh38.p7	15:68612572	TTTTCATACCCTTGA[C/G]TTCCAGGGAGATGGC	10391
rs77193594	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68612941	TTCTGGAGTTCCTTT[C/T]CCAGGTCCAGGACAT	10391
rs77239507	snp	A/G	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68705417	CACCCTAGCCTGGGC[A/G]AAAGGTGAAACTCTA	10391
rs77247036	snp	C/T	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68566110	GATGAGGAGAAGGGG[C/T]TGGGGAGAAAGAGGA	10391
rs77264179	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68591867	GTGGTTATAGCATGG[C/T]GAGAAGAGCACTGGA	10391
rs77273243	snp	C/T	0.0158469	0.0875917	intron-variant	CORO2B	GRCh38.p7	15:68697263	GGGTGTATGACTACA[C/T]TGATGGATAGAGAGA	10391
rs77273879	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640509	CAAAAGGCAATGCTA[A/T]TTAAAAAAAAAAAAA	10391
rs77275634	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68704239	AGCAAGACCGTGTCT[A/G]AAAAAAAAAAAGAAA	10391
rs77294928	snp	C/G	0.0182019	0.0936463	intron-variant	CORO2B	GRCh38.p7	15:68644459	ATGCTGAGAAACCTT[C/G]CTCCAAAGGGTAATC	10391
rs77326114	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68637581	AGGACACTGAGCCTG[A/G]AGAAGGAAGGCGGCT	10391
rs77344388	snp	A/T	0.0170251	0.090679	intron-variant	CORO2B	GRCh38.p7	15:68707782	TTGGGGACAGAAGGA[A/T]TGTGGTGACTACTGA	10391
rs77355943	snp	C/G	0.0185938	0.0946107	intron-variant	CORO2B	GRCh38.p7	15:68564169	GGGGATAGCAAAATA[C/G]TGCAAATTGGCACTT	10391
rs77367507	snp	C/T	0.0410537	0.137264	intron-variant	CORO2B	GRCh38.p7	15:68668550	CGGTCAAGTAAAGAG[C/T]ATGCGGAAGAGTAGT	10391
rs77389753	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68648659	CGTCTCAAAAAAAAG[A/G]AAGAGAGAGAAAGAG	10391
rs77419292	snp	C/T	0.0271762	0.113356	intron-variant	CORO2B	GRCh38.p7	15:68602562	TCTCCCTATCGTGTA[C/T]TATGTTAAACAGGAT	10391
rs77423179	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598542	CAGAAGGAGTTCACA[C/T]CCTAGACTAGAGAAG	10391
rs77437725	snp	C/T	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68719823	GAACTCATTTCAGAA[C/T]GTTGCTGTCATTTGG	10391
rs77444805	snp	C/T	0.00557542	0.0525036	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632229	CACGGCCCATCTGTG[C/T]AGGGTACAGCCTTCA	10391
rs77470797	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68678280	TAGTAAGAGCAGGGG[A/G]AGGAGGAGGAGGAAT	10391
rs77508548	snp	C/T	0.230017	0.2492	intron-variant	CORO2B	GRCh38.p7	15:68701699	TCGTGTTAGCCAGGA[C/T]GATCTCAATCTCCTG	10391
rs77569440	snp	A/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68696252	GAGCCACTGTCTCAA[A/C]AAAAAAAAAAAAGAG	10391
rs77575265	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68629812	AGGAGCTTGGGCTCT[A/T]AACCAGCATGTGTGT	10391
rs77582502	snp	G/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68642053	TTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTCA	10391
rs77601432	snp	A/G	0.0383715	0.133092	intron-variant	CORO2B	GRCh38.p7	15:68686841	GCGGCGGAGGTCACC[A/G]TGAGCCAAGATCGCA	10391
rs77620607	snp	A/G	0.0425829	0.139564	intron-variant	CORO2B	GRCh38.p7	15:68657792	ACGAAAGAAATGTGA[A/G]GTTTCAGTTAGAGGC	10391
rs77627848	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68665018	GTTTACCAGTCTTTT[A/C]TGGCTTCTGGATCTT	10391
rs77666151	snp	C/T	0.0352966	0.128072	intron-variant	CORO2B	GRCh38.p7	15:68644592	GATATGATGATAATA[C/T]CCAGGACTCAGAGAT	10391
rs77694602	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614937	CCTGTGTGTGGAAGT[C/T]GGGTGGGGTGGGGGC	10391
rs77708876	snp	A/G	0.0726307	0.176182	intron-variant	CORO2B	GRCh38.p7	15:68658686	TTCTTTGTCCAGTAG[A/G]CATCATTCCTAAGAC	10391
rs77710418	snp	C/T	0.0437281	0.141251	intron-variant	CORO2B	GRCh38.p7	15:68579619	TCCCTCCAGGGAGTG[C/T]GCGGCGGGAAGCGTC	10391
rs77719062	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618584	ATGAGCAGTGCTCTT[A/C]CTGGGTTATCACACT	10391
rs77737104	snp	A/G	0.039522	0.134904	intron-variant	CORO2B	GRCh38.p7	15:68629709	GCAGCCTCAGTAGGG[A/G]TCAGATCAGGAGGAC	10391
rs77751090	snp	A/G	0.0532157	0.154195	intron-variant	CORO2B	GRCh38.p7	15:68702169	GAAGAGAGGAGGAGG[A/G]TAGTCTGCCTGATTC	10391
rs77844638	snp	A/G	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68618320	AAACATGGGTTGAGC[A/G]TTGCATATATTACAC	10391
rs77856019	snp	G/T	0.0130921	0.0798413	intron-variant	CORO2B	GRCh38.p7	15:68629218	CAATGTCTGAGAAAA[G/T]CATTTAGATCAGAAG	10391
rs77860269	snp	A/G	0.0364509	0.129988	intron-variant	CORO2B	GRCh38.p7	15:68645757	TAGGTATTATACATT[A/G]AGCATCTGCAAAAAT	10391
rs77883606	snp	C/T	0.0364509	0.129988	intron-variant	CORO2B	GRCh38.p7	15:68707109	GGGATTACAAGCGCG[C/T]GCCACCACGCCCAGC	10391
rs77908336	snp	C/T	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68619472	CATCCCCTGGGGCTT[C/T]TGTCGTGGTGCTGGT	10391
rs77931004	snp	A/G	0.0755793	0.179102	intron-variant	CORO2B	GRCh38.p7	15:68649118	CAGTAGCACTGGTCT[A/G]GAATATGATCACACT	10391
rs77948692	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68691400	GGAGGCCGAGGCGGG[C/T]GGATCACGAGGTCAG	10391
rs77957214	snp	C/T	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68642269	GCCCAAGTCACACAG[C/T]AGGGTTGGGATTTGA	10391
rs77990557	snp	G/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68624675	GGCTGGGCATCTCTG[G/T]TTTTTTTTTTCTTTT	10391
rs78006332	snp	C/T	0.0410537	0.137264	intron-variant	CORO2B	GRCh38.p7	15:68667839	TTCCATCTCTGGAAA[C/T]AGAATATGGGGCAGT	10391
rs78019668	snp	A/G	0.0618563	0.164627	intron-variant	CORO2B	GRCh38.p7	15:68557480	GCGGCCAGTCTATCC[A/G]AGGTCATGGCAGAGC	10391
rs78058323	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68624388	CTCTAAAACCAATGA[C/T]AACAACAAAAATGAT	10391
rs78059175	snp	C/T	0.0818113	0.184966	intron-variant	CORO2B	GRCh38.p7	15:68683726	CCTCACCTCCCTCCC[C/T]GCAGAGCATGTTCTA	10391
rs78100029	snp	A/G	0.0829062	0.185956	intron-variant	CORO2B	GRCh38.p7	15:68681515	AAAGGTGGTCATCCA[A/G]ATATTGGGATTGGGG	10391
rs78107796	snp	C/T	0.438806	0.163867	intron-variant	CORO2B	GRCh38.p7	15:68692507	GGAGAATCGCTTGAA[C/T]CCGGGAGGCGGAGGT	10391
rs78110512	snp	A/G	0.0425829	0.139564	intron-variant	CORO2B	GRCh38.p7	15:68690736	TTTATTGCAGCCTAG[A/G]CCTCCTGGGCTCAAG	10391
rs78111726	in-del	-/CCCCCC			intron-variant	CORO2B	GRCh38.p7	15:68575582	TTGTGATCTGCCCCC[-/CCCCCC]GCCTCGGCCTCCCAA	10391
rs78115722	snp	C/T	0.0364509	0.129988	intron-variant	CORO2B	GRCh38.p7	15:68717129	GCCAATATGGTGAAA[C/T]CCTGTCTCTAAACCC	10391
rs78238127	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68709719	GTGTCCTAAATTATA[C/G]TCACATGTGCTCTTT	10391
rs78245114	snp	A/G	0.0360663	0.129354	intron-variant	CORO2B	GRCh38.p7	15:68700013	CTGGGAGGGGGTGGG[A/G]CGTAAAGGAAATGGA	10391
rs78257797	snp	A/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68604633	TTAAAAAAAAAAACC[A/T]CCCTTCTGTGTAAAT	10391
rs78275683	snp	C/G	0.040671	0.13668	intron-variant	CORO2B	GRCh38.p7	15:68560988	GATAGGATCCAAAAT[C/G]GGAATTTAGGAGGGG	10391
rs78310584	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68569412	TTTGGAGACTGGCTT[C/T]TCTCACTTAGTGATA	10391
rs78373754	snp	A/G	0.00953873	0.0683987	intron-variant	CORO2B	GRCh38.p7	15:68677933	TGGAAAAACATGAAC[A/G]TTGGCTGGATTGAGG	10391
rs78385087	snp	A/G	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68706609	TAGACAGAATCCTCT[A/G]CCCCCAAATATCTCT	10391
rs78395934	snp	A/C	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68587213	AAACAAACAAACAAA[A/C]AAAACCCCCTAAGTG	10391
rs78402389	snp	A/G	0.0799831	0.183287	intron-variant	CORO2B	GRCh38.p7	15:68594028	GCACAGGAAATGATA[A/G]TCTGAAGTCAGAATC	10391
rs78408690	snp	C/T	0.0429648	0.14013	intron-variant	CORO2B	GRCh38.p7	15:68697279	TGATGGATAGAGAGA[C/T]GAATGAGTAAAATTG	10391
rs78439517	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68582185	TCTGAAGGACTCCTG[C/T]CCTAACTAGCCTTAG	10391
rs78445174	snp	A/G	0.0193772	0.0965046	intron-variant	CORO2B	GRCh38.p7	15:68606293	GGGAGTTAGGGTGGT[A/G]GGGCTTAGCCAAGCA	10391
rs78454659	snp	C/G	0.0543475	0.155628	intron-variant	CORO2B	GRCh38.p7	15:68700004	CGCTGCAGCCTGGGA[C/G]GGGGTGGGGCGTAAA	10391
rs78499306	snp	A/G	0.0517044	0.152246	intron-variant	CORO2B	GRCh38.p7	15:68609310	GTTCCCTGTCTGAGC[A/G]TTATCTAGCAAAGGA	10391
rs78505843	snp	G/T	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68581785	GACACACTGGGAGCG[G/T]TAGGTAGGGGAGGAA	10391
rs78511891	snp	A/C	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68571972	AGGCTCTCTGCTGAT[A/C]TCTGAAGGAGAGAAC	10391
rs78581724	snp	C/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68627186	AAAATTTCATTTTTA[C/T]TTGTTTATTTGTTTT	10391
rs78584969	snp	C/T	0.0162398	0.0886349	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578174	TGCCCCGAGTCAGGA[C/T]TGGATCAACACACAG	10391
rs78604550	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68692606	AATAAATAAAAAAAA[-/A]TTAACATTAAAATTT	10391
rs78615692	in-del	-/AAAA			intron-variant	CORO2B	GRCh38.p7	15:68695438	ACCAAGGCAGCAAAT[-/AAAA]CCCTGCTGGATTCCA	10391
rs78638261	snp	A/C	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68697837	GCCCAGTGGCCAGCA[A/C]AAGAGGCCTGGGGTC	10391
rs78649110	snp	C/T	0.0193772	0.0965046	intron-variant	CORO2B	GRCh38.p7	15:68568743	AGTTCACAATAAAAT[C/T]GAGCAGAAAATACAG	10391
rs78726358	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68717325	TCAAAAAAAAAAAAA[-/AA]GATTTCTCTGGCTTC	10391
rs78742128	snp	A/G	0.0368353	0.130617	intron-variant	CORO2B	GRCh38.p7	15:68665737	TTATATTTGCTAATT[A/G]ATGATTGTATACTAG	10391
rs78784414	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68694811	TGGTCACTCCAGTGG[A/G]TAGTAACAGCTTAAC	10391
rs78801012	snp	C/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68596074	TGCGGGGAGGTGGGA[C/G]TTGTGCAGGAGTGCT	10391
rs78802777	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68699038	GGACATTGACAGACA[A/G]AAAAAGGGTTAGAGA	10391
rs78837396	snp	A/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68684218	AGAGTCTAAAAACCC[A/C]AGGAGATTACACTTT	10391
rs78879751	snp	G/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68708379	TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT	10391
rs78892642	snp	A/C	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640206	AGCCTCTGTCCATCA[A/C]CTTCCAGAACAAACC	10391
rs78920628	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68604632	TTTAAAAAAAAAAAC[C/T]TCCCTTCTGTGTAAA	10391
rs78926098	snp	A/C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653872	CAGGAAAAAAAAAAA[A/C/T]ATGCCTGAATCTTCA	10391
rs78928017	snp	A/C	0.0952156	0.196321	intron-variant	CORO2B	GRCh38.p7	15:68680365	GATGAAAGTGTGGAT[A/C]ATCTCTTGGGAGGGC	10391
rs78983412	snp	A/G	0.0524604	0.153226	intron-variant	CORO2B	GRCh38.p7	15:68705529	TGGGGATAAAGCAAG[A/G]CACCTCTCTCCCTCT	10391
rs78992606	snp	A/G	0.0376037	0.131863	intron-variant	CORO2B	GRCh38.p7	15:68664430	AGACAGGCGGATCAC[A/G]AGGTCAGGAGATCGA	10391
rs78993396	snp	A/C	0.0263992	0.111815	intron-variant	CORO2B	GRCh38.p7	15:68714144	CCCGCACACCAGCTT[A/C]TCATAGCATTCCCAG	10391
rs79015583	snp	A/G	0.0607341	0.163335	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616193	AATTGGGTTGCTGTC[A/G]GGGATATGGCTAATC	10391
rs79017522	snp	A/G	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68704111	TGGTCATGGTGGTGC[A/G]CATCTGTAGTTTCAG	10391
rs79052899	snp	A/G	0.0825414	0.185628	intron-variant	CORO2B	GRCh38.p7	15:68667848	TGGAAATAGAATATG[A/G]GGCAGTGAAGACCAT	10391
rs79066541	in-del	-/CCC/CCT/CCTG			intron-variant	CORO2B	GRCh38.p7	15:68575446	AGTTCAAGCAATTCT[-/CCC/CCT/CCTG]GCCTCAGCCTCCTGA	10391
rs79080775	snp	A/G	0.230017	0.2492	intron-variant	CORO2B	GRCh38.p7	15:68701701	GTGTTAGCCAGGACG[A/G]TCTCAATCTCCTGAC	10391
rs79081428	snp	A/G	0.0337553	0.125452	intron-variant	CORO2B	GRCh38.p7	15:68715682	AGCCTCTAGGAAGCC[A/G]TGACTCCCAGATCCC	10391
rs79109566	snp	C/T	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68658373	TGGGGGCCTCGTCCC[C/T]GCCTGCCATCTGTGC	10391
rs79167564	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68695595	TATGAACAAGGAGGG[A/G]GGGAGAAAAGGAAGG	10391
rs79186715	snp	C/T	0.0391387	0.134304	intron-variant	CORO2B	GRCh38.p7	15:68692858	AGACTGGTCTCAGAC[C/T]CCTGACCTCAGGTGA	10391
rs79191642	snp	C/T	0.198324	0.244601	intron-variant	CORO2B	GRCh38.p7	15:68720552	ACTTCCAAGTTCACT[C/T]ATGTGGTTGCTGCTA	10391
rs79200420	snp	A/C	0.0111196	0.0737302	intron-variant	CORO2B	GRCh38.p7	15:68717650	AGACTCAGAAAAGTT[A/C]AGCAACTCACCTGAG	10391
rs79282303	snp	C/G	0.0410537	0.137264	intron-variant	CORO2B	GRCh38.p7	15:68669378	GCAGTTGGGCAGATT[C/G]CCTAAAGGGAACAGG	10391
rs79303441	snp	C/G	0.0252325	0.109451	intron-variant	CORO2B	GRCh38.p7	15:68647142	AGAAAAGCTACATGT[C/G]TATTAGAGGAAAATG	10391
rs79306415	snp	A/G	0.0633504	0.166319	intron-variant	CORO2B	GRCh38.p7	15:68635541	CAGGAAGCTTGCAGT[A/G]TGGACCGGTCATCCA	10391
rs79343259	snp	A/G	0.0637235	0.166737	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727876	GTACCTTGATGGTCA[A/G]CTCCCCACCCACAGC	10391
rs79362505	snp	A/G	0.186737	0.241863	intron-variant	CORO2B	GRCh38.p7	15:68563517	AAAGAAAAGAAAAAG[A/G]AAAAAAGAAGAGAAA	10391
rs79400351	snp	A/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68691603	GCACTCCAGCCTGGG[A/C]GACAGAGCGAGACTC	10391
rs79403171	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68704240	GCAAGACCGTGTCTG[A/G]AAAAAAAAAAGAAAA	10391
rs79413458	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68665175	AAAGAATGAGGTATA[A/G]ATTAACTTTTTTTCC	10391
rs79414043	snp	A/G	0.0818113	0.184966	intron-variant	CORO2B	GRCh38.p7	15:68681240	AATTTTTTTTTGGAA[A/G]GAAAAGCTGAGGGAA	10391
rs79436256	snp	A/G	0.0178098	0.0926698	intron-variant	CORO2B	GRCh38.p7	15:68668015	ACACCTGTTGAACAC[A/G]TACAACGGGCCAGGG	10391
rs79438042	snp	C/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68646248	CCATAGCCACTCAGG[C/T]GGAGTCCCCAGAGGC	10391
rs79458049	snp	A/G	0.0158469	0.0875917	intron-variant	CORO2B	GRCh38.p7	15:68722704	CCTCTCAACAGATGT[A/G]ACTGGGACTGGTGGT	10391
rs79459126	snp	C/T	0.0414363	0.137845	intron-variant	CORO2B	GRCh38.p7	15:68674473	TTCCTGTGAGCAAGG[C/T]CTCCAGAACTGACAG	10391
rs79502668	snp	A/G	0.00953873	0.0683987	intron-variant	CORO2B	GRCh38.p7	15:68601993	GAAGGCAGAAGGCCA[A/G]ACACGATGGGAAGGC	10391
rs79512578	snp	C/T	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68682299	AGTTCGAGAAGAGAC[C/T]AGCACCGTGGAGACC	10391
rs79517835	snp	A/G	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68663544	TTTTCTTAACAGGAC[A/G]CAGAAAGCAATAGCT	10391
rs79541700	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68576238	CAGAGGCCGTGACTG[A/G]GCACAAGGGGATGTG	10391
rs79551912	snp	C/G	0.0103295	0.0711199	intron-variant	CORO2B	GRCh38.p7	15:68650760	AATTTCTTACAATCA[C/G]TACTTAACGTTTTGT	10391
rs79561585	snp	C/T	0.0872718	0.189788	intron-variant	CORO2B	GRCh38.p7	15:68581763	TGTGAGAGGTAGGAT[C/T]GCTGCTGACACACTG	10391
rs79562404	snp	C/T	0.0372196	0.131242	intron-variant	CORO2B	GRCh38.p7	15:68671211	AGCTGATACTCACCA[C/T]GACATAATAGGAATT	10391
rs79598982	snp	A/C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68571681	TCCCACACACAAAAA[A/C/T]CATTCGCCCAAGGCA	10391
rs79602498	snp	A/G	0.077417	0.180873	intron-variant	CORO2B	GRCh38.p7	15:68683830	AACCAGGAACCAAAG[A/G]TCCCTCAGTGAGGAA	10391
rs79608223	snp	A/G	0.0364509	0.129988	intron-variant	CORO2B	GRCh38.p7	15:68702043	AGGTCAGCAGCTTGA[A/G]ACCAGCCTGGCCAAC	10391
rs79654001	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68581106	TGGAGACCTGAACCT[A/T]GAAGCAGGGATGGGA	10391
rs79701493	snp	G/T	0.0414363	0.137845	intron-variant	CORO2B	GRCh38.p7	15:68712770	TGTTACTCCTCTCAT[G/T]TGATACGTGAGAACA	10391
rs79713838	snp	C/T	0.0803491	0.183626	intron-variant	CORO2B	GRCh38.p7	15:68679942	GCAAGGCTGAAGTTC[C/T]GAGCCAGAGGTCCCC	10391
rs79717204	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68709717	AAGTGTCCTAAATTA[C/T]AGTCACATGTGCTCT	10391
rs79717893	snp	A/T	0.0166325	0.0896639	intron-variant	CORO2B	GRCh38.p7	15:68611465	ATATTACAACATGGC[A/T]TCAGGAGCGTTTCCC	10391
rs79761281	snp	G/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68713443	CAGTGTCCTATGGCT[G/T]CTGTAACAAATGCCC	10391
rs79805870	snp	C/T	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68677983	AAATCTCCTGCCTCT[C/T]GGAGGCCTGGTGGGG	10391
rs79806506	snp	G/T	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68621495	CCTGAAAGGGGACCT[G/T]CCCAGGGTTCCACAC	10391
rs79861729	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655082	GCCATGGAGCCTGGT[A/G]GTGCCCCTCTCAAGC	10391
rs79890536	snp	A/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68607905	CTCCAGGAACAGATG[A/C]CATGTGACAAGACCC	10391
rs79908796	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68581371	CAGCGTGTTCTTGTG[A/G]GGAACAGAGAGCAAG	10391
rs79940684	snp	A/C	0.0138799	0.0821421	intron-variant	CORO2B	GRCh38.p7	15:68653057	GTTTCCAAACTCCAT[A/C]CAAGTGCAGCAGATC	10391
rs79966394	snp	A/G	0.0158469	0.0875917	intron-variant	CORO2B	GRCh38.p7	15:68603190	GTCTTACACGCCATG[A/G]AAGTCCCAGGGCTAA	10391
rs79968146	snp	A/G	0.214843	0.247516	intron-variant	CORO2B	GRCh38.p7	15:68561796	AGCATGTTTCCGTGG[A/G]TCTGAGAGTATGAGG	10391
rs79980874	snp	A/G	0.0422008	0.138995	intron-variant	CORO2B	GRCh38.p7	15:68647770	CCCAACACTTTGGGA[A/G]GCCAAGGCAGGAAGA	10391
rs79993709	in-del	-/CT	0.0383715	0.133092	intron-variant	CORO2B	GRCh38.p7	15:68688986	CCTATCTGCCAATAA[-/CT]CTGTCTGTTGGCATT	10391
rs80033175	snp	C/T	0.0240643	0.107019	intron-variant	CORO2B	GRCh38.p7	15:68558206	TGCAGGACTACACAG[C/T]GGGGCTGGTGAGCCC	10391
rs80034112	snp	A/G	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68678130	CCAGATGACTTGTAC[A/G]GCACCCGTGCCACTG	10391
rs80079099	snp	C/T	0.0209421	0.100162	intron-variant	CORO2B	GRCh38.p7	15:68594810	CCTTTCAACCTCTTG[C/T]CTCCAGTCCCAGGAA	10391
rs80083176	snp	C/T	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68725413	AATAATGTAATAATA[C/T]ATGTAATACATGTAA	10391
rs80084156	snp	A/G	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68647278	AGTTTCTGTATTACA[A/G]TGAGGCACCTAAACA	10391
rs80108351	snp	A/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68657519	TGAGATCCTGTCTCA[A/C]AAAAAAAAAAAAAAA	10391
rs80122478	snp	G/T	0.181659	0.240478	intron-variant	CORO2B	GRCh38.p7	15:68677397	TAGGGCTAGCTGAAG[G/T]CCACACAGCAGAGGG	10391
rs80140648	snp	A/G	0.0236746	0.106192	intron-variant	CORO2B	GRCh38.p7	15:68711032	ATTCATTCGCTACAC[A/G]CAACTGAGCAACTCC	10391
rs80144490	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68601279	TGGTTGAGATACTGC[C/T]GCTGGGCTCCAGGGC	10391
rs80160990	snp	G/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68702845	TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT	10391
rs80177693	snp	C/T	0.0547245	0.156101	intron-variant	CORO2B	GRCh38.p7	15:68569665	CTCCAGGGAGAACGA[C/T]TGCTGGATCATATGG	10391
rs80193546	snp	A/C	0.0524604	0.153226	intron-variant	CORO2B	GRCh38.p7	15:68702385	AACCCCCTCCCAGGA[A/C]TCACAGCAGTAGATG	10391
rs80208895	snp	A/G	0.0475351	0.146656	intron-variant	CORO2B	GRCh38.p7	15:68681365	GCCTTTCTAAAGACC[A/G]TGTCACAAGGAATGC	10391
rs80211336	snp	A/G	0.02016	0.0983543	intron-variant	CORO2B	GRCh38.p7	15:68594125	CGAATAAACAAAAGG[A/G]GTGTTTGGGGGAGAC	10391
rs80236402	snp	A/G	0.0123036	0.0774623	intron-variant	CORO2B	GRCh38.p7	15:68657777	TGCCTACATTTATAC[A/G]CGAAAGAAATGTGAG	10391
rs80236545	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675348	TTCCTCGGTCAGTTC[A/G]GCCTCTGCTTGGGCC	10391
rs80255651	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68690655	AGCTTTCTTTTTTTT[C/T]TTTTTTTTTTTTGAG	10391
rs80281884	snp	C/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68648428	GAGGCGGGTGGATCA[C/G]AAGGTCAGGAGATCA	10391
rs80291349	snp	C/T	0.0142736	0.0832652	intron-variant	CORO2B	GRCh38.p7	15:68658864	GGCCTGATGAGCCCC[C/T]GTGCAGTGTTTGTGA	10391
rs80308267	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720865	ATCTTAAACTAGACA[A/G]TCTATACCACCAACT	10391
rs111248494	snp	C/G	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68624719	TTTCTTTGAGATAGA[C/G]TCTCGCTCTGTCACC	10391
rs111249770	snp	A/G	0.177182	0.23916	intron-variant	CORO2B	GRCh38.p7	15:68645963	ATTTTCAGTAGAGAT[A/G]GGGTTTCACCATGTT	10391
rs111283715	snp	A/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68689122	GTTCTGTCCCAGCAC[A/C]AAGAAGGGCTGGACT	10391
rs111285800	in-del	-/G	0.078151	0.181571	intron-variant	CORO2B	GRCh38.p7	15:68616781	ACAGGTGTGTGCAGA[-/G]GGATGGCACAGTGTG	10391
rs111291187	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616027	GTGGTTTACATGCAG[C/T]GGCTCGCTCCCTCCT	10391
rs111296231	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68598183	AAGCTCAGTGCCCTG[A/G]GCTCTGTAGGCAGCC	10391
rs111297244	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68605262	GGATCACCCATTTGG[A/G]GAGCAATTTGGCAAC	10391
rs111325928	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68641859	CTCCCAAGTAGCTGA[A/G]ACTATAGGTGTGTAC	10391
rs111330798	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68687907	GAGGGCACAGCCCTC[A/G]TGACCTAATCACCTC	10391
rs111339480	snp	C/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68691397	TTGGGAGGCCGAGGC[C/G]GGCGGATCACGAGGT	10391
rs111349277	snp	A/G	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68703988	CACTTGAGCTCAGGA[A/G]TTCGAGACCAACCTG	10391
rs111368473	snp	G/T	0.00953873	0.0683987	intron-variant	CORO2B	GRCh38.p7	15:68658404	CTCCTTCCTGCCTTC[G/T]GCCAGTGAGGGGCCA	10391
rs111375955	snp	C/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68693948	TCAAGCGATTCTCCT[C/G]TCTCAGCCTCCCGAG	10391
rs111377072	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68708073	ATTATAAAGTTTTTC[A/G]CAAGTGGGCTTTTGA	10391
rs111423862	snp	A/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68652399	AGCCTGATTAACCAC[A/T]GGGGCCTCCCCAGGG	10391
rs111438376	snp	A/C	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68720732	CAAGATGGAAGCTAC[A/C]GTCTTTCTGTCACCT	10391
rs111475210	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68599398	CCTGGCCCTATAGAT[C/G]TTCAATTACAGGTTT	10391
rs111491306	snp	C/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68717106	GTCAGGAGTTCGAGA[C/G]CAGTCTGGCCAATAT	10391
rs111491550	in-del	-/GT/GTGT/GTGTGTGT/GTGTGTGTGT/GTGTGTGTGTGTGT/GTGTGTGTGTGTGTGT	0.427727	0.175821	intron-variant	CORO2B	GRCh38.p7	15:68672159	CTTGGTAATCGGGAG[lengthTooLong]GTGTGTGTGTGTGTG	10391
rs111500535	snp	G/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68567878	TATAAAAATTAGTCG[G/T]GTTTGGTGGCAGGCG	10391
rs111507279	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68694052	CGTTGGCCAGGCTGG[G/T]CTCAAACTCCTGACG	10391
rs111546536	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68558993	GCGTGTCTGTCTTTC[C/T]CTACTTTACCATCTT	10391
rs111560501	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68650406	AAAAAAAAAAAAAAA[A/T]TGGAGACATTCCTGG	10391
rs111560506	snp	A/C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621256	GACAAATCACACACT[A/C/G]CCTCCAGCCCCATGG	10391
rs111570185	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68634085	GCCTGGACTATGAAA[C/T]AGCCTTTTAAAAAAG	10391
rs111597843	snp	G/T	0.0225045	0.103662	intron-variant	CORO2B	GRCh38.p7	15:68601269	GATGTAGAGATGGTT[G/T]AGATACTGCCGCTGG	10391
rs111614295	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68627086	TTCTACGCCTGCAAA[A/G]TGGGCACAATAATGT	10391
rs111635262	snp	A/G	0.077417	0.180873	intron-variant	CORO2B	GRCh38.p7	15:68685699	CAATCCGGGAAACCC[A/G]TTAAAAATACCAATG	10391
rs111665491	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68682654	CAGGAGGGGCAAGGA[C/T]ACCATGTTTATTATC	10391
rs111682021	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68695736	CTGAGAGAAGTGTCC[C/T]GATTTTTCCAAGGAC	10391
rs111684617	snp	C/G	0.314787	0.241459	intron-variant	CORO2B	GRCh38.p7	15:68691101	TTGGGAGGCCAAGGC[C/G]GGTGGATCACGAGGT	10391
rs111694330	snp	A/G	0.0603597	0.1629	intron-variant	CORO2B	GRCh38.p7	15:68650612	TGAGACTCCGTCTCA[A/G]AAACAAAAACTATCT	10391
rs111718536	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68565000	ATCTCTATAAAACCT[A/G]TCCTTATAGTTAAGA	10391
rs111721665	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68575447	AGTTCAAGCAATTCT[C/G]CCTCAGCCTCCTGAG	10391
rs111731264	in-del	-/CAGACTG	0.0248432	0.108648	intron-variant	CORO2B	GRCh38.p7	15:68592146	ACCACACATCCACTC[-/CAGACTG]CAGACTGCCAAGAGT	10391
rs111732667	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68584966	AGGCACAAGTGGGGT[A/G]GGGGTGGGGAGTGGG	10391
rs111753832	snp	C/T	0.0275645	0.114116	intron-variant	CORO2B	GRCh38.p7	15:68688624	AGCGTAGATCTTTAG[C/T]AATGCTCATGCCACT	10391
rs111759015	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68575204	CCTCGGGTCAGCCCT[C/T]AAACAATGGGGAAGA	10391
rs111771138	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68701590	TCCCGGGTTCACGCC[A/G]TTCTCCTGCCTCAGC	10391
rs111787425	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68629862	TGTGTGTTGTGTGCA[C/T]ACACACGCACTATGT	10391
rs111787533	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68576173	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	10391
rs111789763	snp	C/T	0.20511	0.245937	intron-variant	CORO2B	GRCh38.p7	15:68723703	GTGATCCACCCACCT[C/T]GGCCTCCTAAAGTAC	10391
rs111816512	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68585682	GGCTATTGTCTGTTG[C/T]GTTTGTGGCCCTGCC	10391
rs111824791	snp	C/T	0.0325976	0.123435	intron-variant	CORO2B	GRCh38.p7	15:68599863	TGAATTCAGGGACTA[C/T]TAGCCAGGCTCTGTG	10391
rs111829156	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646326	CTTGTTTATGGCTGA[G/T]TTCCCCCTTCCCAGC	10391
rs111838706	snp	C/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68638955	GGCCTCAGCCTGACA[C/G]CAGTACTGGGTTCAG	10391
rs111855926	in-del	-/G	0.178144	0.239451	intron-variant	CORO2B	GRCh38.p7	15:68678067	TCCTTTCCCCTGCAA[-/G]GGTCTGTTGCTTCCT	10391
rs111869399	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68602601	AACCTCCACGGTTCC[C/G]AGGGCTCTGATCAGC	10391
rs111880263	in-del	-/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68593661	CCCTCTCTGGGTTTG[-/T]TTTTTTTTTTTGCAA	10391
rs111881836	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68692643	TTTCCTTTTTTTTTT[G/T]TTTTTTTGAAGACAG	10391
rs111887285	snp	A/C	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68696007	TTTGGGAGGCCAAGG[A/C]AGGAGGATCACTTGA	10391
rs111908323	snp	A/G	0.0158469	0.0875917	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630281	ATGAACTTGACTATC[A/G]CTCCCTCGACCCAAG	10391
rs111909510	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68691314	CAGCCTGGGAGACAG[C/T]GAGACTCCGTCTCAA	10391
rs111911644	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68691557	GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	10391
rs111967342	snp	A/G	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68705311	GGCGTGGTGGTGGGC[A/G]CCTATAATCCCAGTT	10391
rs111998279	in-del	-/A	0.136506	0.222754	intron-variant	CORO2B	GRCh38.p7	15:68704240	GCAAGACCGTGTCTG[-/A]AAAAAAAAAAGAAAA	10391
rs112000422	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68705660	CTTCATTCCATGAGA[C/T]TTGAATCCAGTTAAG	10391
rs112008735	snp	G/T	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68697199	GGATTGTTGGATGGA[G/T]GGATGGATGGATTGT	10391
rs112011168	snp	A/C	0.0310518	0.120672	intron-variant	CORO2B	GRCh38.p7	15:68671900	GTATACTAGGAGGTG[A/C]GATTACAGGAGACCA	10391
rs112057210	snp	A/C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68583883	GTGGGAGCCCACTTG[A/C/T]GGGTGGGCAAGGGCT	10391
rs112061059	snp	A/C	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68715163	TGGGACCAGGCCCTG[A/C]TCTGCCCTCCCTACC	10391
rs112065090	snp	C/G	0.0228947	0.104514	intron-variant	CORO2B	GRCh38.p7	15:68635965	CCCTGCCCTCAACAG[C/G]AGCCAGGATAATTGA	10391
rs112081095	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68718348	CCCTGCCCCTGCTGT[A/G]CTCTGTGACCTTGGG	10391
rs112095350	snp	C/T	0.0729998	0.176553	intron-variant	CORO2B	GRCh38.p7	15:68669822	AGCACTTCAGGAGGC[C/T]AAGGTGGGTGGATCA	10391
rs112149999	snp	A/G	0.081446	0.184634	intron-variant	CORO2B	GRCh38.p7	15:68685663	GGGTAGTGGTTCCCA[A/G]TCTTTGCTGCTCATT	10391
rs112152243	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68598538	AAGCCAGAAGGAGTT[C/T]ACACCCTAGACTAGA	10391
rs112169601	in-del	-/TG	0.180064	0.240019	intron-variant	CORO2B	GRCh38.p7	15:68664355	TAACCTCTTAAAAAC[-/TG]AGAGTTATTGGCGGG	10391
rs112208742	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68608531	GAGTGTGCACGCGTG[C/T]GTGTGTGTGTGTTGG	10391
rs112209851	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68669944	TGCCTGTAATCCCAG[C/T]TACTCAGGAGGCTGA	10391
rs112218238	snp	A/C	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68683084	GGTATGGCAGAAACC[A/C]AGGCCTCTGGGCCAA	10391
rs112228181	snp	C/T	0.0799831	0.183287	intron-variant	CORO2B	GRCh38.p7	15:68723562	CGGGTTCAAGCAATT[C/T]TTTGCTTCAGCCTCC	10391
rs112241991	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68685351	AAGTAGCTGGGATTA[C/T]AGGCACGTGTCACCA	10391
rs112257257	in-del	-/A	0.0872718	0.189788	intron-variant	CORO2B	GRCh38.p7	15:68700395	CAAAACATTCAGAGG[-/A]CACTGGTGGGATTTC	10391
rs112259028	snp	C/G	0.201418	0.245234	intron-variant	CORO2B	GRCh38.p7	15:68721134	TGATCCACCTGCCTC[C/G]GCCTCCCAAAGTGCT	10391
rs112266550	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68605380	GGGGAAAAACTCTAT[C/G]CATCAAGATGCTCAT	10391
rs112281071	snp	C/T	0.5	0	synonymous-codon	CORO2B	GRCh38.p7	15:68719507	GAGTGTTGTGGTCAA[C/T]GGAATAGATTTATTA	10391
rs112284296	snp	C/G	0.5	0	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727906	CTCCTTTGCCTTTCT[C/G]GAATGACAACCCACG	10391
rs112304058	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68702122	GCCCAGGGAAGAAGG[A/G]AAAATCAGGTACGGG	10391
rs112310437	snp	C/T	0.209997	0.246779	intron-variant	CORO2B	GRCh38.p7	15:68692563	ACACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	10391
rs112327403	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68714994	TGTCAGAAAGGCTGT[C/G]TACACACACACACTC	10391
rs112336842	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68582709	CTAAAGTCTAGGCCC[C/T]TGCAACCCGCTTTGT	10391
rs112351790	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68622546	TAATTGCCTTCAGCA[A/G]TGGGGAACTCACCAC	10391
rs112358621	snp	C/T	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68634309	GCATTAGGCCCAGCT[C/T]TTTTACTCACTCGCT	10391
rs112359901	snp	C/T	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68641975	TTCAAGCGATCTGTC[C/T]GCCTCAGCCTCCCGA	10391
rs112387327	snp	A/T	0.0209421	0.100162	intron-variant	CORO2B	GRCh38.p7	15:68672247	TTCTGGTTTTTAAAA[A/T]TTTTTTGAGACAGAA	10391
rs112389689	snp	C/T	0.00914312	0.0669923	intron-variant	CORO2B	GRCh38.p7	15:68607278	AAGGCTGGACTGGGC[C/T]GGGACTGTTGACTGG	10391
rs112409513	snp	C/G	0.0569829	0.158885	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631199	GTGGTGCTTGACTCC[C/G]CATGTCCCCCAAAGG	10391
rs112417396	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68627152	ATTCCTATAAGCTGC[C/T]TCTAAACGTATTACT	10391
rs112480916	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68691498	GGCGTAGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	10391
rs112504446	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68677087	TCCAAGACCTGTTTT[C/T]GCAGCACTTTCGGGA	10391
rs112513638	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68686038	TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT	10391
rs112560753	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68703154	TTTCTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT	10391
rs112600673	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68559155	ACGGGGGCAGGGAGC[A/T]GACCTGACTCAGTGG	10391
rs112620421	snp	A/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68691504	GTGGCGGGCGCCTGT[A/G]GTCCCAGCTACTTGG	10391
rs112659017	in-del	-/A	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68704015	CCTGGGCAATATGGC[-/A]AAAACCCTTTCTCTA	10391
rs112659955	snp	C/T	0.0185938	0.0946107	intron-variant	CORO2B	GRCh38.p7	15:68635073	CAGGTGATTCTGAGG[C/T]AGATGACCTGGGGCT	10391
rs112668592	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68605223	GTTGTATAAGCCATT[A/G]TCAAAGACACATAAA	10391
rs112673362	in-del	-/T	0.0839998	0.186933	intron-variant	CORO2B	GRCh38.p7	15:68645780	GCAAAAATTATACAA[-/T]TTTTTTTTTTTGAGA	10391
rs112674857	snp	C/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68667739	CTGAAGATGGGCGGG[C/G]GGATGTGGAGGAATG	10391
rs112684389	in-del	-/C	0.081446	0.184634	intron-variant	CORO2B	GRCh38.p7	15:68683565	AGTTTTGGTGCACCA[-/C]CCCCTCCCCCCACTG	10391
rs112690984	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68599286	TGAGATAGTTATATC[C/T]GAACATGTCTTGTCT	10391
rs112692960	snp	A/G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68722143	ATAACAAGGGCCTGA[A/G/T]CTCAGTTCTGGCACT	10391
rs112693185	snp	G/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68589933	GTGCATGCCCTACAT[G/T]CCTGGCTGCCCCCCT	10391
rs112721076	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68716982	GTGGGACATGAGACA[A/G]CATGATGGGATCCGA	10391
rs112731384	snp	A/G	0.0792508	0.182605	intron-variant	CORO2B	GRCh38.p7	15:68658314	ATGGAGGAGGAGGGC[A/G]AGATGCATGGTGCTC	10391
rs112744362	snp	G/T	0.0162398	0.0886349	intron-variant	CORO2B	GRCh38.p7	15:68697250	TGGATGGATTGTTGG[G/T]TGTATGACTACATTG	10391
rs112748658	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68627776	ATCTCCCTCTGTCTG[C/T]TTACCCCTGCCATAG	10391
rs112770340	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68655505	CACGACAAGTCCTGA[C/T]CCCAAAAAGGAGAAG	10391
rs112788938	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68670303	CCTCAGCCTCCCAAG[G/T]AGCTGGGACTTCAGG	10391
rs112800324	snp	A/C	0.0267878	0.112589	intron-variant	CORO2B	GRCh38.p7	15:68723184	TGGGGTACAATGGCA[A/C]AATCTTGACTCACTG	10391
rs112805297	snp	A/G	0.000132072	0.00812518	synonymous-codon	CORO2B	GRCh38.p7	15:68711628	CATGTCCTTCAACAC[A/G]GACGGCAGCCTGCTC	10391
rs112838526	snp	A/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68691439	GACCATCCCGGCTAA[A/C]ACGGTGAAACCTCGT	10391
rs112849052	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700598	AGGGGCTTTGGGCCC[A/G]AGGGAGGGCTGGGGG	10391
rs112875756	snp	A/G	0.0818113	0.184966	intron-variant	CORO2B	GRCh38.p7	15:68683748	CATGTTCTACCTCTC[A/G]GCAAGAGAGTGTGGC	10391
rs112878394	snp	A/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68691553	TGGCGTGAACCCGGG[A/G]GGCGGAGCTTGCAGT	10391
rs112880324	snp	C/T	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68705258	GCCTGGCCAACATGG[C/T]GAAACCTTATCTCTA	10391
rs112881977	in-del	-/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68625271	CGTGTCTTCAGCTAA[-/T]TTTTTTTTTTTAACT	10391
rs112897094	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68717644	TCTTGTAGACTCAGA[A/G]AAGTTAAGCAACTCA	10391
rs112933611	snp	A/C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608831	GGGAGTTGAAATTCC[A/C/G]CACTCTCATCCTCAG	10391
rs112940943	snp	A/C	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68628865	TTTCTGCTGAGAGGG[A/C]TGCCCTCAGTTTCCC	10391
rs112987625	snp	A/G	0.109461	0.206758	intron-variant	CORO2B	GRCh38.p7	15:68653586	CATCCTCCCCTGAAA[A/G]CCCTTAGAACGATAT	10391
rs113007856	snp	A/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68691392	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	10391
rs113033652	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721810	TGCAGTGCTGTGGCA[C/T]GATCATAGCTCACTA	10391
rs113109491	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68625355	CACTTCTATGCATTT[C/T]ACAAATGCAAACAAT	10391
rs113160567	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68718932	ACTGGGGTCTTCAAA[C/T]CTAATTTGGGGTGAG	10391
rs113184541	snp	C/G	0.021333	0.101051	intron-variant	CORO2B	GRCh38.p7	15:68676478	TGCAAGGATAACCAC[C/G]GCTGCCTAAACCCGT	10391
rs113198403	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68709319	AACTTCTAGTATTAC[C/T]TTGCCAACACTGGCT	10391
rs113242316	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68697968	TGCTGAGGTGCTGGG[A/G]GAGTGGCGGGAAGGG	10391
rs113242713	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68691517	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	10391
rs113249272	in-del	-/TTTTTTTTTTT	0	0	intron-variant	CORO2B	GRCh38.p7	15:68702822	TTCTTTTTCTTTTTC[-/TTTTTTTTTTT]TTTTTTTTTTTTGAG	10391
rs113257011	snp	C/T	0.200492	0.245049	intron-variant	CORO2B	GRCh38.p7	15:68721445	GCGCCGTAGCTCATG[C/T]CTGTAATCCCAGCAC	10391
rs113268697	snp	C/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68724905	GCGGGTTAAGCTAGA[C/G]AGTCATTGGGGTGAA	10391
rs113280107	snp	A/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68691348	AAAAAAAAAAAGGCC[A/G]GGCGCGGTGGCTCAC	10391
rs113304437	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68719091	CTGACTGAAGAGTAG[A/G]GGCTTTCCCAGCAGC	10391
rs113328791	snp	G/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68627237	TTATTGTATGATTTT[G/T]TGCTGGTCTCGTATG	10391
rs113350849	snp	A/C	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68680593	CAACACAATTTGGTG[A/C]GAGCTTACCATTTGT	10391
rs113354465	snp	A/G	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68704151	AGGCTGAGGTGGGAG[A/G]ATGGCTTGATCCTGG	10391
rs113395200	snp	A/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68561711	GTGCTCTGTCTGTTA[A/T]CGTGTACAGGACTGA	10391
rs113406238	in-del	-/TTTG	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68693825	CAGATCTGGTTGTGA[-/TTTG]TTTGTTTGTTTGTTT	10391
rs113479466	snp	C/T	0.378568	0.214407	intron-variant	CORO2B	GRCh38.p7	15:68691432	AGATCGAGACCATCC[C/T]GGCTAAAACGGTGAA	10391
rs113487269	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68583644	GTCCATAGGAGCCTT[C/G]CTATACCTACAGTCA	10391
rs113499936	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68576169	AAAAAAAAAAAAAAA[A/G]AAAAAAAGAAAGAAA	10391
rs113523919	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68596830	GGGGAGAAATGGCCG[C/T]GCATCACGCAGAGCA	10391
rs113548755	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68685604	GTATTTCAGGTGCTC[C/T]AGGAGGCAGGAGGCC	10391
rs113548876	snp	A/G	0.209084	0.246629	intron-variant	CORO2B	GRCh38.p7	15:68691058	TTTTCGGCCAGGTGC[A/G]GTGGCTCACGCCTGT	10391
rs113550443	snp	A/G	0.469544	0.119585	intron-variant	CORO2B	GRCh38.p7	15:68691202	GGCAAGGTGGCGGGC[A/G]CCTGTGGTCTCAGCT	10391
rs113596318	snp	C/T	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68605326	GTGACCTAGTAATCC[C/T]GCTTCTGGGAACCTG	10391
rs113608884	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68558243	CATCAAACATCTCTA[C/T]ATCCAAGCCCAGCTT	10391
rs113616051	in-del	-/ATTA	0.223819	0.248625	intron-variant	CORO2B	GRCh38.p7	15:68685769	TTAATTGTTTGATTG[-/ATTA]ATTAAACACTTTATT	10391
rs113616594	snp	A/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68669183	GAAAAGAAAAGAAAG[A/G]AAGGAAGCAAGCAAG	10391
rs113649305	snp	C/T	0.0614824	0.164198	intron-variant	CORO2B	GRCh38.p7	15:68688307	TTCTGATGTATTTTC[C/T]TGTAGATTGGTTTTT	10391
rs113650012	snp	C/T	0.0818113	0.184966	intron-variant	CORO2B	GRCh38.p7	15:68681542	GGGGGAGATAATCAC[C/T]ATTTTCATAGGACCT	10391
rs113656375	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68650404	AAAAAAAAAAAAAAA[A/G]AATGGAGACATTCCT	10391
rs113662812	snp	C/T	0.02762	0.114583	intron-variant	CORO2B	GRCh38.p7	15:68718039	TGAGGACTCAAACCC[C/T]GTTGGTCCACCCCTA	10391
rs113671940	snp	A/G	0.0520825	0.152737	intron-variant	CORO2B	GRCh38.p7	15:68562838	AAAAATTAGCCGGGC[A/G]TGGTGGCAGGCGCCG	10391
rs113673368	in-del	-/CA	0.0352966	0.128072	intron-variant	CORO2B	GRCh38.p7	15:68633716	CAACTTCTCCTTTCT[-/CA]CATTTGGGGCACTGA	10391
rs113714174	snp	A/C	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68628036	CCCCACCACCACCCA[A/C]ACCAGCAACATCAGT	10391
rs113735695	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68705436	GGTGAAACTCTATCT[C/T]AAAAAAAAAAAAAAA	10391
rs113757541	in-del	-/A	0.154661	0.231107	intron-variant	CORO2B	GRCh38.p7	15:68604619	TATAAGTTGTGATTT[-/A]AAAAAAAAAAACCTC	10391
rs113818275	snp	C/T	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68701684	AGAGACGGGGTTTCA[C/T]CGTGTTAGCCAGGAC	10391
rs113835286	in-del	-/AG	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68669069	GAAAGAAAGAGAGAA[-/AG]AGAGAGAGAGAGAGA	10391
rs113851434	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648591	GGAGGTGGAGCTTGC[A/G]GTGAGCCAAGATTGC	10391
rs113883607	snp	C/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68599735	ATGACAGTAGTGTGC[C/T]CTCCCCAGGCTCTCC	10391
rs113886133	snp	A/T	0.0205511	0.0992634	intron-variant	CORO2B	GRCh38.p7	15:68565146	TACTGTCTACTGAAC[A/T]TGAATTTAAGATTAA	10391
rs113905053	in-del	-/G	0.0524604	0.153226	intron-variant	CORO2B	GRCh38.p7	15:68574617	GAGGTTATTAAGGTT[-/G]AAGATAAAGGTGCCC	10391
rs113907302	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68573313	AAGAGAAGAGAGAGA[C/T]GTCCACAGAGACAGG	10391
rs113909343	snp	C/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68598857	GAGTGACTCTGCTTG[C/T]GGGAAGCTGGTGGGG	10391
rs113942152	snp	G/T	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68701343	GAGAGACGGAGGCTC[G/T]CTCTGTCGCCCAGTC	10391
rs113953700	snp	C/T	0.0509478	0.151255	intron-variant	CORO2B	GRCh38.p7	15:68703442	AGGTGTGAGCCACCT[C/T]GCCCAGCCCAGAAAC	10391
rs113954720	snp	A/G	0.0770498	0.180522	intron-variant	CORO2B	GRCh38.p7	15:68686829	GCTTGAACCCAGGCG[A/G]CGGAGGTCACCGTGA	10391
rs113972170	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68696087	ACAAAAAATTGAATT[A/T]AAAAAAAAAAAAACT	10391
rs113990519	in-del	-/T	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68604505	ATTAAAAAGGTGTGG[-/T]TTTTTTTTTTAAAAG	10391
rs114052786	snp	C/T	0.0509478	0.151255	intron-variant	CORO2B	GRCh38.p7	15:68707117	AAGCGCGCGCCACCA[C/T]GCCCAGCTGCCGCCT	10391
rs114118515	snp	G/T	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68656423	TGAGCATGAGAGGTG[G/T]AAGGTATGGAGGGGT	10391
rs114187157	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68708231	CATGAGGGAAATGCT[C/T]ATTCTTATAGTATGA	10391
rs114200850	snp	G/T	0.0205511	0.0992634	intron-variant	CORO2B	GRCh38.p7	15:68601941	GCTGCATCCTCCAGA[G/T]GGGGAGGATCACTGT	10391
rs114230678	snp	C/G	0.0150606	0.0854603	intron-variant	CORO2B	GRCh38.p7	15:68558721	CTGCGATATAATAGG[C/G]GAGTGTGGACACGGG	10391
rs114248151	snp	C/G	0.0103295	0.0711199	intron-variant	CORO2B	GRCh38.p7	15:68666338	GGTGTCACGAGGTGT[C/G]AGAAGTAGGGAAGAG	10391
rs114250240	snp	C/T	0.0391387	0.134304	intron-variant	CORO2B	GRCh38.p7	15:68624616	AGACCCAAGAGTTCC[C/T]GGGGTCCATGCCCAG	10391
rs114254220	snp	C/T	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68581849	TAGGGCTCTAGCCTT[C/T]TCTGCTGCTGCTTCT	10391
rs114281235	snp	C/T	0.0138799	0.0821421	intron-variant	CORO2B	GRCh38.p7	15:68635731	ATTTTCCTGGCTCTC[C/T]GTGCAGAGTGAATAT	10391
rs114311636	snp	A/G	0.02016	0.0983543	intron-variant	CORO2B	GRCh38.p7	15:68673375	TCAAATGAAAAAAAT[A/G]AAAAATTAGCCAAGC	10391
rs114325129	snp	C/G	0.0166325	0.0896639	intron-variant	CORO2B	GRCh38.p7	15:68683011	GGTTTTTATAATTTT[C/G]GCAGCGGCCCATGCA	10391
rs114326634	snp	C/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68664814	ATCTATTTGCATTTC[C/T]TTTTTGTGTGAATTG	10391
rs114329302	snp	A/G	0.0205511	0.0992634	intron-variant	CORO2B	GRCh38.p7	15:68638405	TCCAGTGAGCTGGAT[A/G]ACATTATTCTCATTT	10391
rs114333301	snp	C/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68669526	ATGAGTGGGCCAGGG[C/T]TAGGACAGCCAAGAA	10391
rs114334071	snp	A/T	0.108048	0.20579	intron-variant	CORO2B	GRCh38.p7	15:68597653	AAATAAATAAATAAA[A/T]AATAAAAAAGACCAA	10391
rs114368229	snp	C/T	0.0189856	0.0955633	intron-variant	CORO2B	GRCh38.p7	15:68574342	GGTGGAGGAGCATCT[C/T]CCTCTTAGGGGCTCT	10391
rs114370111	snp	A/C	0.0197687	0.0974348	intron-variant	CORO2B	GRCh38.p7	15:68606684	GATATTTTGCTAGCT[A/C]ATGGGTAGAGTGGGG	10391
rs114381402	snp	A/T	0.0861826	0.188849	intron-variant	CORO2B	GRCh38.p7	15:68586946	GAAATTTTCCACCTT[A/T]TATTTTTAGTGGGCT	10391
rs114382476	snp	A/G	0.0123036	0.0774623	intron-variant	CORO2B	GRCh38.p7	15:68718476	AATTCTAAAGCACGC[A/G]CTGTGGTGAGGCAGG	10391
rs114476409	snp	A/C	0.0352966	0.128072	intron-variant	CORO2B	GRCh38.p7	15:68656154	TGCCCACCCCTCCCC[A/C]TCCCCCTCGCACCGT	10391
rs114555647	snp	A/T	0.0150606	0.0854603	intron-variant	CORO2B	GRCh38.p7	15:68592036	CGAGTTTATGCCCTG[A/T]TGCTGCCCAGCCTTG	10391
rs114558814	snp	C/G	0.0252325	0.109451	intron-variant	CORO2B	GRCh38.p7	15:68569849	GCAGATGAGGAAACC[C/G]AGGTGCAGAGAGTGA	10391
rs114701273	snp	C/T	0.0569829	0.158885	intron-variant	CORO2B	GRCh38.p7	15:68608477	GCCCAGCCCTCTCCC[C/T]CAGGGAGCCCCCATC	10391
rs114714088	snp	A/G	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68669466	CCAGCCTGGTGGGTG[A/G]GATGTGTTCTCTGAC	10391
rs114724101	snp	G/T	0.0123036	0.0774623	intron-variant	CORO2B	GRCh38.p7	15:68666251	AAAACCTGGCACATG[G/T]CAAGTCAACAGATGA	10391
rs114734751	snp	A/G	0.030278	0.119257	intron-variant	CORO2B	GRCh38.p7	15:68655295	CTTGGAGTCTAGCTG[A/G]CTCAGATGGAGGCAC	10391
rs114760836	snp	A/G	0.0298908	0.118541	intron-variant	CORO2B	GRCh38.p7	15:68646249	CATAGCCACTCAGGC[A/G]GAGTCCCCAGAGGCC	10391
rs114869359	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68626997	GTGTAGCAAGACTCC[C/T]GGGTTCAGCTCCCAG	10391
rs114873887	snp	A/T	0.0372196	0.131242	intron-variant	CORO2B	GRCh38.p7	15:68626150	TCTTCAGCAATTTTT[A/T]AAAAATGTTCCTACT	10391
rs114895745	snp	A/G	0.0696718	0.173152	intron-variant	CORO2B	GRCh38.p7	15:68583736	CCAGGAGATACCTGA[A/G]CCTCCAGACATTCTA	10391
rs114896214	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68716805	AGGGAGGTCAGTGTG[A/G]CTGAGCGTGGTGTAG	10391
rs114896876	snp	C/T	0.0158469	0.0875917	intron-variant	CORO2B	GRCh38.p7	15:68654405	TCATTCCTTGCAGAG[C/T]CAGGGAGGCTGGAAA	10391
rs114918800	snp	A/G	0.0547245	0.156101	intron-variant	CORO2B	GRCh38.p7	15:68706813	TTCCTGGGCTCAAGC[A/G]ATCTTCCCCTGCCTT	10391
rs114937651	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578017	CTCTGCTAACTCCTC[C/T]CCTCCACCCTCTCCG	10391
rs114940390	snp	C/T	0.0134861	0.0810011	intron-variant	CORO2B	GRCh38.p7	15:68652610	GTCCCAGCTGTACAC[C/T]GGGTCTCTGGGGCTG	10391
rs114941389	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68618488	AAAAGGGGAAAGGCA[A/G]CCAGATGGAAGCAAC	10391
rs114956180	snp	C/T	0.02016	0.0983543	intron-variant	CORO2B	GRCh38.p7	15:68559766	CCACGTGCAGCTCCA[C/T]GGCGTGCCCACCAGG	10391
rs115029048	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68591825	ATAGGAGGGGGCAGA[A/G]GACCAGAAGTTTCCT	10391
rs115079077	snp	A/G	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68594632	TGAGAAAGGGGCTCT[A/G]TTTATTGAACTCATC	10391
rs115086957	snp	G/T	0.0166325	0.0896639	intron-variant	CORO2B	GRCh38.p7	15:68670206	TTGAGACAGGATCTG[G/T]CTTTGTTGCCCAGGC	10391
rs115105106	snp	A/G	0.0154538	0.0865337	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615040	GGAGCTGGGCTTCTC[A/G]ATGCTGCCTCTGAGA	10391
rs115118695	snp	C/T	0.0547245	0.156101	intron-variant	CORO2B	GRCh38.p7	15:68707066	CCCAGGTTCCAGCGA[C/T]AGTCCTGCCTCAGCC	10391
rs115146105	snp	G/T	0.0333238	0.124705	intron-variant	CORO2B	GRCh38.p7	15:68696915	CAGAGCCTGGGTACC[G/T]GTCAGATTTTCAGGA	10391
rs115161743	snp	C/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68700178	TCAACTTGCTGCTCA[C/G]CAGACACGACATCCA	10391
rs115165296	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639839	GTCTTGCGCCTTGTG[C/T]TCATTGGTCCTAAAA	10391
rs115168748	snp	A/G	0.0138799	0.0821421	intron-variant	CORO2B	GRCh38.p7	15:68589059	CCTTACTCATTAAAA[A/G]ATCTGGGAACAAACT	10391
rs115173502	snp	A/G	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68573554	GAAGTGTGGGGAGGT[A/G]CAAAGCATGGAAAGG	10391
rs115189101	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616199	GTTGCTGTCGGGGAT[A/G]TGGCTAATCAGAATT	10391
rs115221079	snp	A/G	0.00953873	0.0683987	intron-variant	CORO2B	GRCh38.p7	15:68601516	GAGCGTGCAGTGCGA[A/G]GAGGGCTAGGATGAG	10391
rs115239156	snp	A/G	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68606137	TAGTTTAGCTCTACC[A/G]TGTTAGGTCAAAGGT	10391
rs115268678	snp	A/G	0.0352966	0.128072	intron-variant	CORO2B	GRCh38.p7	15:68656415	TCGTCAGGTGAGCAT[A/G]AGAGGTGGAAGGTAT	10391
rs115284899	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68562008	CTTGTCCCTTCTCTA[C/T]CCTAAAGGCAGGCCA	10391
rs115295104	snp	A/G	0.0360663	0.129354	intron-variant	CORO2B	GRCh38.p7	15:68723414	GGTGTGAGCCACGGC[A/G]CCCAGCCAATAGATA	10391
rs115323662	snp	C/T	0.029116	0.117091	intron-variant	CORO2B	GRCh38.p7	15:68598344	GTGTGTGCACGTAAG[C/T]GTGTGCTTTGGTAGG	10391
rs115379469	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68608485	CTCTCCCTCAGGGAG[A/C]CCCCATCCACTTCCT	10391
rs115420412	snp	A/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68673036	ACACCCCCAGGGAAA[A/G]GGTCTACAAACAAGT	10391
rs115429497	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68571353	TTTAATACAAATAGA[A/T]CCCTAAGAGCCATGG	10391
rs115447351	snp	A/G	0.0168055	0.0901129	intron-variant	CORO2B	GRCh38.p7	15:68716471	TGTACCAGACCCTGC[A/G]CGAAGTCCAGTGGCA	10391
rs115447447	snp	G/T	0.0189856	0.0955633	intron-variant	CORO2B	GRCh38.p7	15:68665414	TAATATCAACAGGGA[G/T]AGTCACCACTCATTG	10391
rs115452072	snp	G/T	0.0228947	0.104514	intron-variant	CORO2B	GRCh38.p7	15:68699356	TCCAGGGAACCAAGG[G/T]GACCTGTGTGGATGG	10391
rs115460685	snp	A/T	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68660913	TTGTTCTCTCTATAG[A/T]GGTTCTCTTTCTTAG	10391
rs115463091	snp	A/G	0.00953873	0.0683987	intron-variant	CORO2B	GRCh38.p7	15:68619273	TGCCTTAGATCACCT[A/G]CCCTCACTTTCCTTT	10391
rs115484090	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68569875	AGTGAAAGGCTTGCC[C/T]AGGGAGTGGCAGAAT	10391
rs115517446	snp	C/T	0.0103295	0.0711199	intron-variant	CORO2B	GRCh38.p7	15:68673888	TAAGACCCACAGCAC[C/T]GTGGGTGACTAACTA	10391
rs115532977	snp	A/G	0.0252325	0.109451	intron-variant	CORO2B	GRCh38.p7	15:68646702	TAAAAGCAGGATCAG[A/G]AATCCTCCTCTGCCT	10391
rs115583231	snp	A/G	0.0168055	0.0901129	intron-variant	CORO2B	GRCh38.p7	15:68712045	AGGCACAGGAGGAGG[A/G]GACACTGGACTCACT	10391
rs115659377	snp	C/T	0.0524604	0.153226	intron-variant	CORO2B	GRCh38.p7	15:68704232	GTGAGAGAGCAAGAC[C/T]GTGTCTGAAAAAAAA	10391
rs115667536	snp	G/T	0.0513262	0.151752	intron-variant	CORO2B	GRCh38.p7	15:68700070	GAGGTCAGCACTGCT[G/T]CCAGGGCCCTTCCCA	10391
rs115671014	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68637122	CACGACACACTCCTC[A/G]CATGATTCTGATGCA	10391
rs115683580	snp	A/G	0.0138799	0.0821421	intron-variant	CORO2B	GRCh38.p7	15:68644014	TGCACTCCAGCCTGG[A/G]TGACAGCCCCATCTC	10391
rs115703826	snp	A/C	0.00914312	0.0669923	intron-variant	CORO2B	GRCh38.p7	15:68695319	TGCTTCCTTTGGAGG[A/C]CTCTCTTCCTACCCT	10391
rs115747246	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68583018	CTTTCATGCCAACAT[C/G]CTCCTCCCTGCTAAG	10391
rs115747914	snp	A/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68561713	GCTCTGTCTGTTATC[A/G]TGTACAGGACTGAAA	10391
rs115800764	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68696575	AAAAAAAAAAAAAAA[A/G]AATCCAGGGAAAGTG	10391
rs115806862	snp	A/C	0.0376037	0.131863	intron-variant	CORO2B	GRCh38.p7	15:68622667	CAAGATTCACCCCCA[A/C]ACCCCATTCATTCAT	10391
rs115814503	snp	C/T	0.0119091	0.0762411	intron-variant	CORO2B	GRCh38.p7	15:68660138	TATGGTACCAATTCT[C/T]CTTTGACCATGTGCC	10391
rs115822260	snp	A/C/T	0.0521629	0.153225	intron-variant	CORO2B	GRCh38.p7	15:68706190	GACCCCCGTGCAGGT[A/C/T]CCCTACCTGCTGGCG	10391
rs115830203	snp	C/T	0.0146672	0.084371	intron-variant	CORO2B	GRCh38.p7	15:68652747	TATACTCATTCTCCT[C/T]GTTTTACAGATAAAG	10391
rs115879030	snp	A/G	0.0170251	0.090679	intron-variant	CORO2B	GRCh38.p7	15:68659902	CCTGGGTGACAGAGC[A/G]AGACTGTGTTTCAAA	10391
rs115886614	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68667423	TTCCTGCTTCTAGGC[A/G]ATGGGCTCCTTGAGG	10391
rs115954096	snp	C/T	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68719880	TAACAGGGGCAAGCC[C/T]GGCCTCGTGTATCAC	10391
rs115971024	snp	A/G	0.0368353	0.130617	intron-variant	CORO2B	GRCh38.p7	15:68626232	AACCATAACGCAGGA[A/G]GGGGCTTGAGTGTAA	10391
rs115973758	snp	G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68582151	ACAGCTGCTAAAGCT[G/T]CCGGCAAACCCTGTG	10391
rs115983305	snp	C/T	0.0704125	0.17392	intron-variant	CORO2B	GRCh38.p7	15:68691032	TGTTTGATGTCTCTA[C/T]AGAAAACTGGTTTTC	10391
rs115997609	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68678849	TCCAGTGCTCAGATA[A/G]GGAAGAACTAGAGTA	10391
rs115997762	snp	C/T	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68673051	GGGTCTACAAACAAG[C/T]TGTAGCTTACAGGGG	10391
rs116000588	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68647872	TAAAAAAAAAAAAAA[A/G]AAAAAAATTAGCCGA	10391
rs116000681	snp	C/T	0.0103295	0.0711199	intron-variant	CORO2B	GRCh38.p7	15:68605219	CAAAGTTGTATAAGC[C/T]ATTATCAAAGACACA	10391
rs116052705	snp	C/T	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68668116	TAGCTTATACAAAGT[C/T]GCACAGCTGGGAAGT	10391
rs116053590	snp	A/G	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630231	TTGCTGGACCCAGGG[A/G]ATGCTGTGTGGGGTG	10391
rs116064800	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587254	GGTGTCTGCTCTGTC[C/T]GAGCTCAGAGAAGGT	10391
rs116064995	snp	G/T	0.0185938	0.0946107	intron-variant	CORO2B	GRCh38.p7	15:68564494	ATTTTATTTTTTGTA[G/T]TTTTAGTAGGTTTTG	10391
rs116108198	snp	A/G	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68699909	GTTCAGATTCATCAC[A/G]CTCAACATTTACATC	10391
rs116146278	snp	A/C	0.0170251	0.090679	intron-variant	CORO2B	GRCh38.p7	15:68649239	GTATTTGATATATAT[A/C]TTTTTTCAACTTTAT	10391
rs116153334	snp	A/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68595298	GCCCTGCTGTCCTGT[A/G]TCCCTGAGAACACTG	10391
rs116209066	snp	C/T	0.0418186	0.138422	intron-variant	CORO2B	GRCh38.p7	15:68622824	AACACCCCTGTGAGG[C/T]AGGCAGAAGAGATTA	10391
rs116211688	snp	C/G	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68572472	TGTTGCCTGAGAGAT[C/G]GAAGGTGAAAACAAC	10391
rs116303028	snp	C/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68660349	CCTCTAGTGTGATGT[C/G]TGTTAGCTCTTAAGC	10391
rs116335300	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68593871	GAGCCATCCTGACCT[A/G]AGAAGGGCGAGAGAA	10391
rs116373621	snp	C/T	0.00101392	0.0224929	intron-variant	CORO2B	GRCh38.p7	15:68695300	GTGGGCTCAGGCCCC[C/T]CCCTGCTTCCTTTGG	10391
rs116393778	snp	G/T	0.0562307	0.157967	intron-variant	CORO2B	GRCh38.p7	15:68626359	GGTTTTTCTTAAAGA[G/T]CCTGACTTTTAAAAA	10391
rs116458895	snp	A/G	0.030665	0.119967	intron-variant	CORO2B	GRCh38.p7	15:68708323	AGCCTTGCTCCCAGG[A/G]CTTCTGGTCTGCCTT	10391
rs116461874	snp	C/T	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639611	TCTATTATCTCAGGG[C/T]TGGAAGGCAATCTAA	10391
rs116522776	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68581986	TATGGACTGCAGGAG[C/T]TCTGAGCTCAGAGAG	10391
rs116524233	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68719852	GGAGTTCCAGGAGTT[A/G]TAAATTCCTGACTAA	10391
rs116526449	snp	A/G	0.0225045	0.103662	intron-variant	CORO2B	GRCh38.p7	15:68687845	ATAACAAACCCACTC[A/G]CAAGACAACTAACCC	10391
rs116528047	snp	A/G	0.030278	0.119257	intron-variant	CORO2B	GRCh38.p7	15:68690637	AAGCAATGTGATCAC[A/G]TTAGCTTTCTTTTTT	10391
rs116538637	snp	A/G	0.0444908	0.142359	intron-variant	CORO2B	GRCh38.p7	15:68702488	ATATTGGCAAACAGT[A/G]AGTCCAGTGCTCAGA	10391
rs116560396	snp	C/G	0.0170251	0.090679	intron-variant	CORO2B	GRCh38.p7	15:68668057	CTCTTGAGACGCCTG[C/G]TGCCACTGAATACTC	10391
rs116588340	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68675908	GGCCTACACGCTAGC[A/G]GAGGAGACAGATAAT	10391
rs116609364	snp	C/T	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68613820	TGAAACTCCTGAAAG[C/T]CTTAGTAAGAACACT	10391
rs116674976	snp	A/G	0.0185938	0.0946107	intron-variant	CORO2B	GRCh38.p7	15:68672058	CAGGAATAGTGAACC[A/G]GGGTGAAAAGATCCC	10391
rs116682827	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68701018	GGATGGACAGGATGT[C/T]AGCCCTGCTGGAAGC	10391
rs116704388	snp	A/G	0.0162398	0.0886349	intron-variant	CORO2B	GRCh38.p7	15:68581045	CTGCTCTGCATCGTT[A/G]GGCATCCTGGCTACT	10391
rs116710467	snp	C/T	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68569405	TGTAGCCTTTGGAGA[C/T]TGGCTTCTCTCACTT	10391
rs116714803	snp	C/T	0.0111196	0.0737302	intron-variant	CORO2B	GRCh38.p7	15:68682826	GTAGCAGTGCTTTAG[C/T]AATGCTCCCCAAATC	10391
rs116755020	snp	C/T	0.0498117	0.149749	intron-variant	CORO2B	GRCh38.p7	15:68706751	GTCTCACTCTGTCAC[C/T]CACACTAAAGTGTAG	10391
rs116763226	snp	C/T	0.0479149	0.147179	intron-variant	CORO2B	GRCh38.p7	15:68604522	TTTTTTTTTAAAAGG[C/T]GACTTTATCTCAGCA	10391
rs116803901	snp	C/T	0.0232847	0.105357	intron-variant	CORO2B	GRCh38.p7	15:68613246	AACTGAGACTATTAC[C/T]ATGAGAGAGAATAGA	10391
rs116831207	snp	A/G	0.0134861	0.0810011	intron-variant	CORO2B	GRCh38.p7	15:68717512	ACTTGCTAAGGTATC[A/G]GATATGGAGGGGTGG	10391
rs116856221	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68681198	AGCCTGGGCGAGAGA[A/G]CAAGATCTCCCTCCA	10391
rs116857188	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609572	CGAATCCACATCTCT[C/T]TTGGAGTTGGGGGAG	10391
rs116892847	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68585400	AGTTATTAAGCAGGC[A/G]TTGGGCACGCATGAT	10391
rs116899626	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640304	CTGCCCTCTCCTCTC[C/T]TTTCGCATGCTTTAC	10391
rs116943292	snp	A/G	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68725091	TTATCAGCACAAGCC[A/G]GGCATGGTAGCTTAC	10391
rs116960175	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68698425	GACCAGTCCTAGCTC[A/G]GCGTCTTATTTAACC	10391
rs116961088	snp	A/T	0.124444	0.216185	intron-variant	CORO2B	GRCh38.p7	15:68662030	AATAAATAAATAAAT[A/T]AATTAATTAATAAAA	10391
rs117034698	snp	A/G	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68612104	GAAGCATCCCTGAAC[A/G]AGAAATGTGTCCACA	10391
rs117050264	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68560886	CCGCAGCTCTCCTCA[C/T]GATCTTGTGGGGACT	10391
rs117076357	snp	C/T	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68605500	CAATGGAATATTCTG[C/T]AGCCGTTAAAAATTA	10391
rs117175387	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68606999	GGGCACTACAAGAAG[A/G]AGCCTTCTCCAAACA	10391
rs117210367	snp	A/G	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68656248	TGTGGGAGGAAGAAG[A/G]GTTGGTCCCAGCATT	10391
rs117212679	snp	A/G	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640874	GAGCAACTGGTGCTT[A/G]GAGCAGCAAAGTGTC	10391
rs117249052	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68595283	TCCTCCTCCAGCTAA[G/T]CCCTGCTGTCCTGTG	10391
rs117344731	snp	A/C	0.0252325	0.109451	intron-variant	CORO2B	GRCh38.p7	15:68565056	TTCATGTGAAAGTAA[A/C]TTTTCGAAGTTACCA	10391
rs117348298	snp	G/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68721404	GGTGGCAGTAGAGGC[G/T]AAGTAAGAATGGTCA	10391
rs117362663	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68663397	TTCATGTGCATGCAG[G/T]TACGTCTGTAGAATA	10391
rs117371705	snp	A/G	0.0178098	0.0926698	intron-variant	CORO2B	GRCh38.p7	15:68674950	GGTGGAGCACGAAAG[A/G]AATGAATCCCTAATA	10391
rs117408117	snp	A/G	0.0130921	0.0798413	intron-variant	CORO2B	GRCh38.p7	15:68612340	ATGATCGTAAGGACA[A/G]ATCAGTAGTGAATGA	10391
rs117422192	snp	A/G	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639648	TCACTGTTCCACATC[A/G]TCCTTAATCGGAGGT	10391
rs117426703	snp	C/T	0.0178098	0.0926698	intron-variant	CORO2B	GRCh38.p7	15:68713103	GGAAATCAAGTGTCA[C/T]GAGCCAGTGGGCAGG	10391
rs117445822	snp	C/T	0.0197687	0.0974348	intron-variant	CORO2B	GRCh38.p7	15:68595965	AGGCCAGGGCAGCGA[C/T]GCCGTGGGGTGCTCC	10391
rs117486863	snp	C/G	0.0298908	0.118541	intron-variant	CORO2B	GRCh38.p7	15:68559724	CCCAGGGGGACTGTC[C/G]GTGAGGCTGCGGCGC	10391
rs117504253	snp	G/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577105	TTGCACAGAGGAGAC[G/T]CCTGAGGTCTGCAGC	10391
rs117507157	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68688031	ATCCATTGGTAACAA[A/G]GGTGTAGAGAAACCT	10391
rs117640202	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68589196	GCATGTGATCCCTGG[C/T]ATACCAGCCAGCAGG	10391
rs117640463	snp	C/T	0.0104728	0.0716012	intron-variant	CORO2B	GRCh38.p7	15:68725798	TCCTTGTCTCACCTG[C/T]TCTCTCCTGGGCCCT	10391
rs117659488	snp	A/G	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68602744	TCTCTACATCAGTGA[A/G]GGAGGTTCTGTGCAA	10391
rs117674718	snp	C/T	0.0123036	0.0774623	intron-variant	CORO2B	GRCh38.p7	15:68668173	TGCTGGCTAAGAGTT[C/T]AGCACCATGCCTGAC	10391
rs117703036	snp	C/T	0.0310518	0.120672	intron-variant	CORO2B	GRCh38.p7	15:68636067	CTGGACAAACCCAGA[C/T]GCATCTGGAAATGGG	10391
rs117760481	snp	A/G	0.0275645	0.114116	intron-variant	CORO2B	GRCh38.p7	15:68686131	CAACCTTCACCTCCC[A/G]AGTCAAGTGATTCTC	10391
rs117781576	snp	C/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68626571	TGGCTGACACAGATG[C/T]GGGACTCCCAGCCTT	10391
rs117812260	snp	A/G	0.0232847	0.105357	intron-variant	CORO2B	GRCh38.p7	15:68712194	AAGTGCCATTTGGAA[A/G]TAAGAAATTACCATT	10391
rs117813868	snp	A/T	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68613897	TATTTTTGCTTTTCA[A/T]TTATAAATTGCTGTG	10391
rs117891606	snp	C/T	0.0123036	0.0774623	intron-variant	CORO2B	GRCh38.p7	15:68560418	TCCCACCCCAGTGTC[C/T]GGAGTAGCTGGGACT	10391
rs117923299	snp	A/T	0.0111196	0.0737302	intron-variant	CORO2B	GRCh38.p7	15:68592909	TATGTTTTAGTCCAT[A/T]TTCTGCTTCTGTAAC	10391
rs118015140	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68610004	ACCCACCCTCCTTCT[C/T]TTGATAAAACCTGGC	10391
rs118040864	snp	C/T	0.0165278	0.0893908	intron-variant	CORO2B	GRCh38.p7	15:68685722	TACCAATGCCTGGCT[C/T]CTGCCTCTCAGATAT	10391
rs118064581	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68683016	TTATAATTTTGGCAG[C/T]GGCCCATGCACACAG	10391
rs118088130	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68608528	TGTGAGTGTGCACGC[A/G]TGCGTGTGTGTGTGT	10391
rs118110949	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68566284	GCCGTCATTATCCCC[A/G]TTTGATAGGAGAGGA	10391
rs118151369	snp	C/T	0.0162398	0.0886349	intron-variant	CORO2B	GRCh38.p7	15:68663611	AAAACTTTTGCTCAT[C/T]GAAAGATTCATTAAC	10391
rs118168738	snp	G/T	0.0197687	0.0974348	intron-variant	CORO2B	GRCh38.p7	15:68593518	GAAACACAATCTGGA[G/T]CCTCGTTCTCTAGAC	10391
rs118175895	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68659935	ACAAAAAAAGTCTAT[C/T]CTCATCTTCATGCTG	10391
rs137864563	in-del	-/ATGTCTATA	0.0755793	0.179102	intron-variant	CORO2B	GRCh38.p7	15:68649182	TGTTCTTTACAGAGT[-/ATGTCTATA]TATAGAAATATGCTA	10391
rs137878454	snp	A/G	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68562640	TAACTGGATCACAGA[A/G]AAATCACAAGAGAAA	10391
rs137900922	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68698200	GCTCGCTGCAAAGCC[C/T]ATGCTCTGCCAAGCT	10391
rs137907699	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68598786	TCTGGGGGTTTGTAC[A/G]GAAACGCTGCCAAAA	10391
rs137913871	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631505	TGTGAAGCCATCCTC[C/T]GTTTGGCCCACTTTG	10391
rs137940030	in-del	-/T	0.0818113	0.184966	intron-variant	CORO2B	GRCh38.p7	15:68682445	CTGACTACAGAGAGG[-/T]TACAGGGAGTCTCAG	10391
rs137946864	snp	A/G	0.0232847	0.105357	intron-variant	CORO2B	GRCh38.p7	15:68634605	CCAAAGTCTGGTTCC[A/G]GGACCAATAGCTTCA	10391
rs137986627	snp	A/C	0.0170251	0.090679	intron-variant	CORO2B	GRCh38.p7	15:68662333	CCTGCACCCACATAA[A/C]AGCTGTATTTTCACA	10391
rs138062957	snp	A/G	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68627248	TTTTGTGCTGGTCTC[A/G]TATGAGGGATTCAGA	10391
rs138088647	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68655955	TTGCCTGGCTTGAAA[C/T]AGAGCATCTCCCTGG	10391
rs138088700	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68697277	ATTGATGGATAGAGA[A/G]ACGAATGAGTAAAAT	10391
rs138094356	snp	G/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68587981	CTTACTGTGTGACCT[G/T]GGGCTAGTCCCTGGA	10391
rs138122643	snp	A/T	0.00531609	0.0512814	missense	CORO2B	GRCh38.p7	15:68711639	ACACGGACGGCAGCC[A/T]GCTCACCACCACGTG	10391
rs138146278	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68693570	CTGAGAGATGGAAGC[A/T]TAGCTTCTGCCTATT	10391
rs138190062	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68685312	TCCTCCTGGGTTCAA[A/G]CCATTCTCATGCCTC	10391
rs138195842	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571224	CCAGCCACCTGTTCT[A/G]TACTCAGTACTCAAT	10391
rs138211516	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68659111	AGGACCTGCAGTGGA[C/T]GGTCTGCCTTTCAAT	10391
rs138214762	snp	A/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68585325	GCCAGAACCTTTTCA[A/T]TCCGATCACATAATG	10391
rs138252602	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727036	CTGAGATGAGGCCTC[A/G]TCCTCCTGGAAGCTG	10391
rs138252702	snp	A/G	0.00914312	0.0669923	intron-variant	CORO2B	GRCh38.p7	15:68681486	TGTGTTTCTGTCAGA[A/G]AAGAAGTCTGGGAAA	10391
rs138254367	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68705512	AAGTGGCTGGTATCA[A/G]ATGGGGATAAAGCAA	10391
rs138272640	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68614270	CCCAATTCTGCTTCT[A/G]TAGAGATAGTTGCAA	10391
rs138298225	snp	C/G	0.0755793	0.179102	intron-variant	CORO2B	GRCh38.p7	15:68650311	GCGGTGAGCTGAGAT[C/G]GCGCCACTGCTCTCC	10391
rs138330771	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68668014	CACACCTGTTGAACA[C/T]GTACAACGGGCCAGG	10391
rs138335896	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68612380	TGTGTGAGAGGAGGT[A/G]TGCGTGAGAAGGGGC	10391
rs138337700	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68618174	TTATATATACAAAAC[A/G]AAACCAAAGGTCATG	10391
rs138369718	snp	A/C	0.0182019	0.0936463	intron-variant	CORO2B	GRCh38.p7	15:68602793	TTCCTGAGAACACTA[A/C]GAAGCAATTCCTCTC	10391
rs138418027	snp	A/C	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68596167	CGAAGTCATTAGATT[A/C]CACAACAATAAATCT	10391
rs138459605	snp	C/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68566082	CCTTCCCCATGCCTG[C/T]GTGCCCTGCCTGGAT	10391
rs138459610	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680617	CATTTGTGTCCAGCA[C/T]GATTCCAGACACTGG	10391
rs138463081	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697816	GGAGCTGGTGGAGGC[C/T]GGAGAGCCCAGTGGC	10391
rs138467925	snp	A/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68641768	TCGGCACTGTCGCCC[A/G]GGTGGTAGTGCAGTG	10391
rs138503920	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68676762	CAAGATCTGTGTTTT[C/T]TGTTTCTTCTGGATT	10391
rs138515669	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667865	GCAGTGAAGACCATG[A/G]GCTTCGGGACCTGTA	10391
rs138522223	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631222	CCCAAAGGCCAGCCA[C/T]TTGCCCGTCAGTGGG	10391
rs138546616	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662623	GATGATTAGCCTCAC[A/G]TGCATTTTAAGCAGA	10391
rs138567253	snp	A/C	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639712	GGAAGCTGACTACCT[A/C]TCAAGGTAGCTTCTT	10391
rs138616303	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68584676	TGGTGTCCAGGAGAT[G/T]AGAACGTGTGCAGAT	10391
rs138618093	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68588553	GCACAGTCCTACCTG[A/G]GTCCCTGGGCAGAAA	10391
rs138691674	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68677526	TCTGGGAAAGGCCAG[A/G]TGGTGGCGGGGGGAT	10391
rs138720567	snp	A/G	0.00199481	0.0315187	downstream-variant-500B	CORO2B	GRCh38.p7	15:68728159	CGGTTAAGAACCACT[A/G]TTCTACCGCTATTCA	10391
rs138745922	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68688593	AAACTGTATAGAACT[G/T]GATTCTGTTTTACTA	10391
rs138754752	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68623931	TGTTGGGAAGATGCC[C/G]TTTCTAATTCCTCCT	10391
rs138800882	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68650624	TCAAAAACAAAAACT[A/G]TCTGTTTACCTATCT	10391
rs138805222	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613583	GCTTGTTAAGAACCA[A/G]TGACGCACAATGCCA	10391
rs138812922	snp	A/G	0.0185938	0.0946107	intron-variant	CORO2B	GRCh38.p7	15:68626987	AGCACAGGATGTGTA[A/G]CAAGACTCCTGGGTT	10391
rs138839440	snp	C/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68617983	AGCATCTACTATGTC[C/G]CAAGCTTCCTACTAA	10391
rs138845347	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68647331	CTTGACTACAATATT[C/T]GCAATATATAATAGA	10391
rs138869240	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68659254	AGGGATAAGGGCGCT[A/G]ACCCCTGCACCATTG	10391
rs138887067	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68635434	ATGCTTCCCTGAGTG[A/G]GTGCTATTCTGCCAC	10391
rs138917422	snp	A/G	0.0387552	0.1337	intron-variant	CORO2B	GRCh38.p7	15:68648645	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAGAA	10391
rs138950906	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68570894	TCCTCCAGCCTCAGC[C/T]GCCCACAGTGCTGGG	10391
rs138951312	snp	A/C/G	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68624425	ATCAACAGTGAGCAC[A/C/G]ACTACCAACACAAAT	10391
rs138954850	snp	C/G	0.0119091	0.0762411	intron-variant	CORO2B	GRCh38.p7	15:68646076	ACTGCACCTGGCCCA[C/G]TCATTTTTTTTTTAA	10391
rs138971128	in-del	-/CAAG	0.314787	0.241459	intron-variant	CORO2B	GRCh38.p7	15:68690922	GGCCTCCCAAAGTGC[-/CAAG]TGGGATTACAGGTGT	10391
rs139048370	in-del	-/A	0.441021	0.161279	intron-variant	CORO2B	GRCh38.p7	15:68692598	CAAAAGCAAATAAAT[-/A]AAAAAAAATTAACAT	10391
rs139058025	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68657159	AGTCTAGAAAAACCC[A/G]TAGACCCCTTCACAG	10391
rs139108505	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68621214	GGAGGTGCCAGGACC[C/T]GTGCTCATGGCTGGA	10391
rs139129270	snp	G/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68681766	CACACTGGCTGAGTG[G/T]CCCAAATCTCTGTCT	10391
rs139141361	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568361	TGTATAGAGTGCCTA[A/G]CACAGTGCCTAGACA	10391
rs139153258	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585963	GCTTGGTTCAGAGAA[C/T]GCAGGTCCCTGGTCC	10391
rs139197340	snp	A/G	0.0256215	0.110247	intron-variant	CORO2B	GRCh38.p7	15:68669019	GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGACCAC	10391
rs139213613	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614616	ATGAGAGGAAAGCCC[C/T]GGAGCCCTCACGGTC	10391
rs139215802	snp	C/T	0.000692087	0.0185894	intron-variant	CORO2B	GRCh38.p7	15:68715196	CCACCTTCCTCAACT[C/T]CATCTCTCCTGACCC	10391
rs139221067	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68589293	AGCTTGCTGAAGCTA[A/G]AGATTAGGTCTGATT	10391
rs139224217	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68607222	GAATCATCTGGAAGT[A/G]CCTTCACACTCATGT	10391
rs139226293	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68558913	ACACACCGCGGGGAG[A/G]TGTTGTGAGAAATAA	10391
rs139280534	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68710979	CTTCCTAAGCAACCA[A/G]TATGGCCTCATCTGT	10391
rs139301253	snp	A/G	0.0130921	0.0798413	intron-variant	CORO2B	GRCh38.p7	15:68643109	GAAATCATGGATTTG[A/G]CATGCAAGTTATATT	10391
rs139303840	snp	A/C	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68699823	AGTCTGCACTCTCAG[A/C]CCCTCACCAGTGGCC	10391
rs139320363	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642412	TAGAAACAGGCCTTG[C/T]GCAGACCATCCCCGG	10391
rs139335081	in-del	-/TTT			intron-variant	CORO2B	GRCh38.p7	15:68692642	TTTCCTTTTTTTTTT[-/TTT]GTTTTTTTGAAGACA	10391
rs139336042	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678650	CTGTACTCCAGCCTG[A/G]GCAAAAGAGCGAGAC	10391
rs139359069	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68676492	CCGCTGCCTAAACCC[A/G]TCAAATGCCAGACAC	10391
rs139389867	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68591787	CCTGGGCTGCCAGAT[A/G]GTTCGATCTAAGGGT	10391
rs139445914	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575569	TCGAACTCCTGACCT[A/T]GTGATCTGCCCCCGC	10391
rs139483695	snp	A/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68683153	GACGGAGCTCCACCC[A/G]CCCAGGGTCCTCCAT	10391
rs139495338	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68625007	TTTAACTCCAGTGCT[A/G]GTGGTCGAAGACCAC	10391
rs139504865	in-del	-/T	0.0962929	0.197165	intron-variant	CORO2B	GRCh38.p7	15:68701240	AGGCTCAGGAGTCCC[-/T]TAGGCCTAGGTTCAA	10391
rs139544672	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68597628	TGTTTCCCCCCCATC[-/A]AAAAAAAAAAAATAA	10391
rs139554042	in-del	-/CG			intron-variant	CORO2B	GRCh38.p7	15:68709456	AAAAGATTTTTTTTT[-/CG]TGTTTTTTTTTTTTT	10391
rs139569922	snp	A/G	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68637603	AAGGCGGCTTGTCCC[A/G]GGTCACATAGCTAGA	10391
rs139572510	snp	A/T	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68563711	ATTGGGGACAATACT[A/T]CCAACCTTACAGAAA	10391
rs139587326	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68686385	TTTACTTGGTGTCTC[A/G]TCTACATCCTGAAAC	10391
rs139617494	snp	C/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68703978	GTGGGCAGATCACTT[C/G]AGCTCAGGAGTTCGA	10391
rs139634127	snp	A/C	0.0158469	0.0875917	intron-variant	CORO2B	GRCh38.p7	15:68566987	GATCCCCACTCTCCC[A/C]CTTGGGTCTGAGGTT	10391
rs139638590	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68573476	GTGCGCCTCTGCCAG[G/T]CCAGAGAGCAGGGAA	10391
rs139648038	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647746	GGTGCCGTGGCTCAC[A/G]CCTGTAATCCCAACA	10391
rs139685467	snp	A/G	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68563351	AAAAATTAGCTGGGC[A/G]TATTGGCGTGTGCCT	10391
rs139688838	snp	A/G	0.0193772	0.0965046	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640081	CTGTTCCCTGCCTGC[A/G]CACCCATGCATCTGA	10391
rs139703763	snp	A/C	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68652252	CCTGTTTTTTCCCCT[A/C]GTTAACATTCAGCTG	10391
rs139717794	snp	A/G	0.0142736	0.0832652	intron-variant	CORO2B	GRCh38.p7	15:68580766	TAATGGATGGGCCCG[A/G]CTAGAGAGAGAAAGG	10391
rs139756369	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68694950	CAGTCTTGGGGAGGA[C/T]ACAGCTGCAGAGCAG	10391
rs139776218	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68625793	TATTTTTTGTAGAGA[C/T]GGGGTTTCACCATGT	10391
rs139789900	snp	A/G	0.000149292	0.0086385	synonymous-codon	CORO2B	GRCh38.p7	15:68725869	GTTCTTCCGGCAGCA[A/G]GATGAGATTCGACGG	10391
rs139835081	snp	C/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68668531	AACTTGAATGGGATG[C/G]AGCCGGTCAAGTAAA	10391
rs139869174	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631965	CAGCATCGCTGGAGT[A/G]GGCTCTCTCTTGGTT	10391
rs139877101	snp	C/T	0.0558544	0.157504	intron-variant	CORO2B	GRCh38.p7	15:68697786	GGTTGCTTCCTGGGC[C/T]GGGAAAGAGGCACAG	10391
rs139898557	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718547	AGACTGATTGAAGGC[A/G]CCCCGGTCTACCCCC	10391
rs139898717	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68673567	TCTTGGCCGGGCTCC[A/G]TGGCACATGCCTGTA	10391
rs139915484	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68608830	GGGGAGTTGAAATTC[C/T]GCACTCTCATCCTCA	10391
rs139931663	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713021	CTGAATATGTGCACT[A/G]CCCCATTGGCCTCTT	10391
rs139950725	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68628605	ATGGTATGAGCAAAG[C/T]AATGTTACAGTTACT	10391
rs139971449	snp	A/G	0.0123036	0.0774623	intron-variant	CORO2B	GRCh38.p7	15:68677858	GGCCAAGTCCCCTCT[A/G]CTGTGTCAAGAACAG	10391
rs139975012	snp	A/G	0.000153988	0.00877328	synonymous-codon	CORO2B	GRCh38.p7	15:68719146	CCTCCCACTGTAGTC[A/G]GATTCCTACCAGGAA	10391
rs139979643	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68672416	GTTTGTATAACAGCC[A/G]GGACATAGATGTGCA	10391
rs139986880	snp	C/T	0.0356815	0.128715	intron-variant	CORO2B	GRCh38.p7	15:68605988	CTTGACCTCCCAAAG[C/T]GCTGGGATTATAGCA	10391
rs140047835	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68713668	CACACCTTCTCCCCT[C/G]TGTGTCTCTGTAATC	10391
rs140093716	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68606212	CCTAGACCAGGAGTG[A/G]GAATTTTGGAGCCAT	10391
rs140110651	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699096	TCCGGTGTGCTTGGC[C/T]TGGAGAGAATGCATA	10391
rs140110979	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68657604	TCTATCAATGCATTA[C/T]GCCCCATGATTGAGT	10391
rs140124204	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68590586	GGGTGCTGCGGGGCC[A/G]CTGGTTTAGAAGGTC	10391
rs140136922	snp	A/G	0.00953873	0.0683987	intron-variant	CORO2B	GRCh38.p7	15:68559788	CCCACCAGGGGGCGC[A/G]GCCCGCATCCTTCCT	10391
rs140182220	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68660382	CTTCAAGATTCATAT[C/G]TTTTTTTTGGCAGGC	10391
rs140195588	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587321	CTTACTGTCCCCTGT[A/C]TGAGATAAGTGTCAA	10391
rs140232923	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68645075	CTGCACCTCTGAGCC[A/G]CAGCTTCCCTCCCCC	10391
rs140238426	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68633763	ACTCTAACAGAGATA[C/T]TACAACGGAGCCGGC	10391
rs140263217	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68653064	AACTCCATACAAGTG[C/T]AGCAGATCTTGGGGA	10391
rs140276049	snp	A/G	0.00080052	0.0199905	missense	CORO2B	GRCh38.p7	15:68725970	ACAGCCCCAAGAACT[A/G]TTAGCTCCCCAGCTG	10391
rs140284147	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68675138	TGAAATTGGGAAATA[C/G]AGCAGAAGGTAATCT	10391
rs140291879	snp	A/G	0.00993419	0.0697739	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615474	CCTGAGCCATTGGCT[A/G]TGGCTTAGGCTTAGA	10391
rs140318149	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68720653	CTCAGGTCCCTGCCA[C/T]GTGGACTCCTCCATA	10391
rs140380181	snp	A/G	0.00057889	0.0170032	synonymous-codon	CORO2B	GRCh38.p7	15:68695244	CATTGCCTCGTGCTC[A/G]GAGGACACGTCGGTG	10391
rs140406129	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68656522	GGTTGCACAGCTAGT[A/T]AGTGCCCCATGTGTC	10391
rs140464148	snp	A/G	0.00023139	0.0107537	missense	CORO2B	GRCh38.p7	15:68645322	ATCGTCACCGAGAGC[A/G]CAGGGGGCGGCTCCT	10391
rs140466788	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654541	TGCTACCCATTTTCC[G/T]TCTAGGGCCTGGAGC	10391
rs140479644	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68598081	TCAGATCCAGACCCC[A/C]TCCACCACCTGGATC	10391
rs140516108	snp	C/T	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68583943	CCTCCTCTCCCTTCC[C/T]GGCCTTCTTCCAGAT	10391
rs140516326	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68618027	AGTTGAACAGAGTCA[A/G]TACCTGCCCTCCAGG	10391
rs140530313	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68649864	TATGCAGCCTTTGGA[A/G]AACCCCACTATACAC	10391
rs140566747	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68620599	GGAACACCTGGTCCC[A/G]CATCTTGCTTTTGAA	10391
rs140637529	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68725090	ATTATCAGCACAAGC[C/T]GGGCATGGTAGCTTA	10391
rs140661851	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582657	AATAGAGTCGTGTGT[A/G]AAGTACAAGTTAATG	10391
rs140672659	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68703559	CAGATCTTCTCCTAG[C/T]TGCTTAGGCCCATGG	10391
rs140700741	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621610	GGTTGGTTACCAGAG[C/T]CTTGTGAGAAGAGAT	10391
rs140702451	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68564750	TCCTTCTAAAGTAAA[C/T]GGTCAAATCATATCA	10391
rs140705184	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68597129	GCTCATTTCAAATTG[C/T]GTAAAACCAAAGAGC	10391
rs140712057	snp	A/C/G	0.00159649	0.0282165	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641216	CCCAGGCCCATCCCC[A/C/G]GGGAACACGCTGAGT	10391
rs140733692	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68576493	GCGGGAAAGGTGCCA[A/G]GAGGCATGCTGGGAG	10391
rs140738691	snp	A/G	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68700481	GTGAAATCAATCCCC[A/G]TCCCCCAGGATCCGT	10391
rs140748690	snp	A/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68705154	CAATGTCAAAGCAGA[A/G]AAGTTTGGAAGATTA	10391
rs140802722	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598943	GTCTGGAGCTGGTCT[A/G]GACTAGGAGAGTGAG	10391
rs140838540	snp	A/G	0.0103295	0.0711199	intron-variant	CORO2B	GRCh38.p7	15:68697469	TCCATCAGTTCACAC[A/G]CTGGGGGTGAGGTCA	10391
rs140849033	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68637109	AGATACATGCCTTCA[C/T]GACACACTCCTCACA	10391
rs140869300	snp	C/T	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630889	GCAAAGGCGGGAAGC[C/T]GTGTGTGTGCCAGTA	10391
rs140892469	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68667706	TCAGTTTCCCCATCT[C/G]TGAGATGGGAGAGTG	10391
rs140892536	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68707686	AGAAGTGTGTGTGTC[C/T]ATATGTCTGTGTCTG	10391
rs140949749	snp	A/G	0.0205511	0.0992634	intron-variant	CORO2B	GRCh38.p7	15:68658425	TGAGGGGCCAGTGGG[A/G]GTTGTGGTTGGGGCC	10391
rs140976937	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68600041	GGGCTGGCAGAGGGA[A/G]TAGAGACAGTTTCTG	10391
rs141001684	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561267	ATATGCCACGCTGGG[A/C]GGCCCCCCTCCCAGC	10391
rs141010602	snp	A/C	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68623047	GTGGGCACCTGTAAT[A/C]TCAGCTACTCTGGAG	10391
rs141017501	in-del	-/GCTG	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68641994	TCAGCCTCCCGAGGT[-/GCTG]GGATTACAAGAGTGA	10391
rs141021846	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68605117	GACTCCGTCTCAAGG[-/A]GAAAAAAAAAAAAAA	10391
rs141035839	snp	C/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68669674	AAATATCAATCCAAT[C/G]GTGGGTTTTGGGCTC	10391
rs141042471	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68570684	TCCCAGTTACACTGA[A/G]GGGAATAGTCAGTGT	10391
rs141053357	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68724161	GAGCCAAGATCGCGC[C/T]ACTGCACTCCAGTCT	10391
rs141080919	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68602122	TCACATTGGCACCGT[C/G]TGAGTTCTGGTGGAG	10391
rs141117291	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68617856	ATGGGGCCCTTAGAG[A/T]TTGTGGCTGAATGTG	10391
rs141167701	snp	G/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68688226	TTTTAATAACAATTT[G/T]ATATGTTTGTTAGAA	10391
rs141191902	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68565722	GAGAGGTATTTGTCT[A/G]TAGCCCTAAGGAACC	10391
rs141195585	in-del	-/TAAAT	0.122064	0.214785	intron-variant	CORO2B	GRCh38.p7	15:68665546	ATTATGTTAAATTGA[-/TAAAT]TAAAGAGAATGTCAA	10391
rs141218768	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576964	GAGAGCCATTGGGCT[A/G]GAGTTGTCAGGAGAG	10391
rs141229894	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68656591	CCATTTCCCACTCCT[C/T]CTTCCCCCACCAAGA	10391
rs141231689	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68652039	GTACAGCCATCCCCA[C/T]CTCACACTTGGGGAA	10391
rs141234542	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68709666	CTCGCTGTGTTGCTC[A/G]TGCTGAAAGATTCTT	10391
rs141256850	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569974	GGCTGAGGAGTCATT[G/T]GTCAGTGGGGTCTGT	10391
rs141265413	snp	A/G	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68614276	TCTGCTTCTATAGAG[A/G]TAGTTGCAAGTGGAT	10391
rs141293248	snp	C/G	0.0252325	0.109451	intron-variant	CORO2B	GRCh38.p7	15:68650495	TGCGTGCCTGTAATC[C/G]CAGCTACTTGGGAGG	10391
rs141316590	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68594794	GGAGAGGACAGAAAG[C/T]CCTTTCAACCTCTTG	10391
rs141338115	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629931	AGAGTCCTTTAAAAA[C/T]CAGGAATCCAAAAGG	10391
rs141383504	snp	A/G	0.0134861	0.0810011	intron-variant	CORO2B	GRCh38.p7	15:68722580	ACACCTCACTAAAGC[A/G]GTTTTTTTGACAAAA	10391
rs141416436	snp	A/G	0.02016	0.0983543	intron-variant	CORO2B	GRCh38.p7	15:68566567	CCCGGCGGACTCTTC[A/G]TGGTCCCAGATGCTT	10391
rs141422261	snp	C/T	0.0221141	0.102801	intron-variant	CORO2B	GRCh38.p7	15:68642235	TAGATGGAAGTGGCA[C/T]AGAGAGGTTAAGTGA	10391
rs141424064	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68696986	GTCTTCCCAGACTGG[A/T]CTGTGAGCTCCTGGG	10391
rs141494399	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68681364	GGCCTTTCTAAAGAC[C/T]GTGTCACAAGGAATG	10391
rs141525164	snp	A/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68699332	TGGTGCATGGGAGAC[A/G]CTACACGCTCCAGGG	10391
rs141527256	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68639319	GGCCAGAAGGAGTTG[C/G]ATGATCTGGTAACTT	10391
rs141550534	snp	C/T	0.0236746	0.106192	intron-variant	CORO2B	GRCh38.p7	15:68667947	TTTCTTATTTGTAAA[C/T]GAGAGATAATAAATC	10391
rs141574313	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68665567	AAAGAGAATGTCAAC[C/T]TTATGATGTTGAGTC	10391
rs141610367	in-del	-/AGGGAA			intron-variant	CORO2B	GRCh38.p7	15:68696580	AAAAAAAAAGAATCC[-/AGGGAA]AGGGAAAGTGAAATT	10391
rs141616020	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627789	TGCTTACCCCTGCCA[C/T]AGACCCTCAGGCTTA	10391
rs141619351	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626225	AGATGAGAACCATAA[C/T]GCAGGAGGGGGCTTG	10391
rs141637030	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660154	CTTTGACCATGTGCC[G/T]GTATCATGGGAGGGT	10391
rs141665097	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558143	GCTGGGCCAGCCTGG[C/T]GGAGGGCAGATAAGA	10391
rs141670338	snp	C/T	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68635118	CTGTTCCCCAGAGCT[C/T]GAGCTTGCAGACCAT	10391
rs141682012	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68628987	TTTGCCTCCAGATGG[A/G]GCAGGGAGAAATGAA	10391
rs141685270	snp	A/G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631355	TCGAGCTCCAAAAAG[A/G/T]TTATGAACTTGTCTA	10391
rs141700557	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68676593	GAACTAGAGTCCATG[A/G]GACTCTCAAGCTGGA	10391
rs141702437	snp	G/T	0.0166325	0.0896639	intron-variant	CORO2B	GRCh38.p7	15:68720920	GAGACAGAGTCTCAC[G/T]CTGTTGCCCAGCCTG	10391
rs141707862	snp	A/G	0.0418186	0.138422	intron-variant	CORO2B	GRCh38.p7	15:68624824	AGTAGCTGGGATTAC[A/G]GGTGCCTACCACCAC	10391
rs141738556	snp	C/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68572910	AGGAGGCTGCCCTGG[C/G]GTTTCCTCACTGTGC	10391
rs141739616	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727762	TGATTATTTATGCTG[C/T]CTCCCAAGGATAGAA	10391
rs141754053	snp	A/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68612105	AAGCATCCCTGAACG[A/T]GAAATGTGTCCACAC	10391
rs141766536	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68715847	CCCACATTCTCCCAC[C/G]ACTAAAAGTCTTACA	10391
rs141779644	in-del	-/A	0.0287284	0.116357	intron-variant	CORO2B	GRCh38.p7	15:68606061	GCAGCTGGGTGGGTG[-/A]AGCCTCGTTTACTGA	10391
rs141807114	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68588006	CCTGGATGTCTCTGA[A/G]CGTCTGTGAAAATGA	10391
rs141811392	snp	C/T	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68619944	TGAGACAGAGTCTCA[C/T]TCTGTCTCCCAGGCT	10391
rs141812404	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68686161	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	10391
rs141829195	snp	A/G	0.021333	0.101051	intron-variant	CORO2B	GRCh38.p7	15:68681568	GACCTGAGACATCAC[A/G]TTTAAAATTGGGTCT	10391
rs141847159	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68680540	TGCAACTGTACAGGG[A/G]ATCCTGATTAGGTCC	10391
rs141882023	in-del	-/CC	0.457271	0.139781	intron-variant	CORO2B	GRCh38.p7	15:68637745	GAGTTCTCCTGGGCT[-/CC]CCCCACATTACACAG	10391
rs141883452	snp	G/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68677043	CCTCCCAAAATGCTG[G/T]GATTACAGGCATGAG	10391
rs141915373	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716940	ATTTGATAAGGAAAT[A/C]ATTATGGGGAGGGTT	10391
rs141961422	in-del	-/TT/TTT	0.452719	0.146304	intron-variant	CORO2B	GRCh38.p7	15:68692632	ATTTAAAAACTTTCC[-/TT/TTT]TTTTTTTTTTGTTTT	10391
rs141982749	snp	C/T	0.000115398	0.00759512	synonymous-codon	CORO2B	GRCh38.p7	15:68715238	AAACATCCGGTACTA[C/T]GAGATCAGCACTGAG	10391
rs141986412	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563048	AGGATTCATTGAAAA[C/T]AGTGGTTAGAAGGAA	10391
rs142001764	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671396	TATGAGCCAAAGCCT[C/T]ACCCACATGGCTTAC	10391
rs142018716	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608677	CCTAGGGAGGGAACT[C/G]CCCATGAACAAGCAT	10391
rs142032133	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68606775	TATGTTTCCTCTGAT[A/G]TCTTTGGTCAGCTTC	10391
rs142062120	in-del	-/CAGATGGAGGGTCAGAGCAGTGGGGC	0.44638	0.154709	intron-variant	CORO2B	GRCh38.p7	15:68580373	AGCCCAGAGTGGGGT[-/CAGATGGAGGGTCAGAGCAGTGGGGC]CAGATGGAGGGTTGG	10391
rs142082178	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68614190	AACACATCTTAATGT[A/G]TTATCAGGGTGGTTC	10391
rs142098367	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68610280	TCTAGCGCCTCGCCT[C/T]GTTTACAAAGCAAAT	10391
rs142135982	snp	G/T	0.0142736	0.0832652	intron-variant	CORO2B	GRCh38.p7	15:68585893	AGGGCATTCAGCCGA[G/T]GGCAGAACAAAGTAT	10391
rs142176846	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640541	GGTGATAGGAGTATT[A/G]TAGGTTAAAGAAGGC	10391
rs142205259	snp	A/G	0.0547245	0.156101	intron-variant	CORO2B	GRCh38.p7	15:68706984	TCTTTTTTTTGAGAC[A/G]GAGACTCACTCTGTC	10391
rs142226512	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662625	TGATTAGCCTCACAT[C/G]CATTTTAAGCAGATA	10391
rs142265147	snp	G/T	0.0865458	0.189163	intron-variant	CORO2B	GRCh38.p7	15:68661762	CTGTAATCCTAGCAC[G/T]TTGGGAGGCCGAGGC	10391
rs142324239	snp	C/G	0.0314385	0.121371	intron-variant	CORO2B	GRCh38.p7	15:68560941	GGGTTTCCCATGGCA[C/G]AGCCCGGGTAATTTT	10391
rs142332386	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68637217	GTCCATGCACCTCCC[A/G]TTGTCTGTTTGGCTT	10391
rs142366144	snp	C/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68701811	CTTTACCTCTGAGTA[C/G]CAGTTGCCCTATTGT	10391
rs142368821	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68692672	AGAGTCTCACTCTGT[C/T]GCCCAGACTGGAGTG	10391
rs142396718	snp	G/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68587717	TATGTATTAATTCAT[G/T]TAAGCTTCATGACAG	10391
rs142398737	snp	A/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68632371	TAAAACGCATTCAGC[A/T]CGGTCCAGTAGAGTT	10391
rs142433787	snp	C/G	0.0232847	0.105357	intron-variant	CORO2B	GRCh38.p7	15:68590349	ACAACAAAGCTCTTC[C/G]GAGGCTGCCCCCCCA	10391
rs142448715	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631869	CCTGAGCTGCCAGGA[A/G]GAGGTGCTCCTCGCA	10391
rs142466441	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592350	ATACCCCACCTGTGC[G/T]TGTTCTGTCTATTTC	10391
rs142477129	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68687746	ACGATGCAGGCATCT[A/G]GCAACGGCCTTCCTG	10391
rs142498024	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68595942	GAGGGAAGGAGCAGC[A/G]TGAGCAGAGGCCAGG	10391
rs142520769	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68610248	GGAGCTAGGACTTCA[C/T]AGGACGAGACAGGTT	10391
rs142548814	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68679009	CCTGACCTGGCCCTC[C/T]GAGCTGGTCAGGCAG	10391
rs142577933	snp	A/G	0.0130921	0.0798413	intron-variant	CORO2B	GRCh38.p7	15:68647596	CTGGAGGCTGAGGCA[A/G]GGGAATCGCTTGAAC	10391
rs142582332	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68720232	TTCCTGGCTGTGACT[A/G]AGCAAGTCTACTGAC	10391
rs142639565	snp	C/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68718000	TAACTTGCCAAAGGA[C/T]TCCTAGATGGAAAGG	10391
rs142664942	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68673467	AGGCTGCAGTAAACT[A/G]TGATCATGCCACTGT	10391
rs142668835	snp	C/T	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68708613	GTGATCCGCCCACCT[C/T]GGCCTCCCAAAGTGC	10391
rs142723177	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68670076	AAAAAAAAGGGGGGG[-/A]AAAATAAAGAAAAAT	10391
rs142797204	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68696877	TTTAGTCAGGCCACA[A/G]GCATCTACCTGGTGC	10391
rs142807687	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68585131	GCTCAGGCTGTCTTT[C/T]GTACAGAATACATAC	10391
rs142812812	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690127	TAGTGGAAATATTCT[A/G]TAATAGTGTGCTGAG	10391
rs142833603	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68567181	CTCCAACCCCCCTTC[A/G]GCTCTCAGTGGGCTC	10391
rs142838177	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68642910	CAACACCTCCTTTCT[C/T]GTCTGTGGAAACTGT	10391
rs142869406	snp	A/G	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68624519	TGGAACTGATATTAG[A/G]AACTACCGTCCCTTG	10391
rs142893904	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68571487	GGACCTGAACAAGAA[A/C]AGATAATTCTTGGAC	10391
rs142899966	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647063	CACAAGGGTCAACAA[A/G]CAATACCTCACATCA	10391
rs142929144	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68663484	CACACACATACACGC[G/T]CACACACACGCAGAA	10391
rs142935040	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68616968	ACTAAAGTTTACAAA[C/T]ACTAGGTATTTAACT	10391
rs142996755	snp	G/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68653730	AAGGTGCCCAGCTCA[G/T]TACTGAGGACTGTAA	10391
rs143009182	snp	C/T	0.000116323	0.00762547	synonymous-codon	CORO2B	GRCh38.p7	15:68718735	GGATGTGTCAGCCTG[C/T]GAGGTGTTCCGCTTC	10391
rs143037956	snp	A/G	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68698356	AATCACTGGCCACCC[A/G]GGTTCCTCCTCAGGT	10391
rs143065412	in-del	-/AAAC	0.225893	0.248835	intron-variant	CORO2B	GRCh38.p7	15:68644032	ACAGCCCCATCTCAA[-/AAAC]AAACAAACAAAAAGA	10391
rs143077946	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68638647	GAAGATATGTGTTGT[A/G]TTGGAAAGAGCAGTA	10391
rs143085627	snp	C/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68711068	ACCCTGTCATTCCTG[C/G]GGTCCACAGAGGCCG	10391
rs143087713	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668404	AAGGGCGCAAACAGT[C/T]GTTAAGATTACATCA	10391
rs143108970	snp	A/T	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68594495	CATGGCCTGGTGAAC[A/T]CTAATTCCTTGGGCA	10391
rs143129223	in-del	-/C	0.0513262	0.151752	intron-variant	CORO2B	GRCh38.p7	15:68689206	TAAGGGTTATAGACT[-/C]CAAAGAATAGGTCTC	10391
rs143153155	snp	A/G	3.31658e-05	0.00407208	missense	CORO2B	GRCh38.p7	15:68725918	CAGAAGGACATCCGC[A/G]TTCGGCAGCTCCAGC	10391
rs143153657	snp	G/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68706434	AGCAGGCATGGGCAA[G/T]TTCAACACCACACCC	10391
rs143198758	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689196	AAGATCTCCCTAAGG[C/G]TTATAGACTCCAAAG	10391
rs143211535	snp	A/G	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68562850	GGCGTGGTGGCAGGC[A/G]CCGGTAGAACCAGCT	10391
rs143216086	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68626077	CAAGAAATGCAATTT[A/G]TTTGATTCATATGTA	10391
rs143228736	snp	G/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68672237	ATGCATAATTTTCTG[G/T]TTTTTAAAAATTTTT	10391
rs143235958	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68713067	AACTTACCTGATGCC[A/G]AGGACTGTTGTGTGT	10391
rs143252683	snp	C/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68613171	TGGCCAACACTTTAT[C/G]GCATGACCACATACT	10391
rs143270333	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680696	TTCTAATTTGAAGGT[C/G]AGAAAGACTAAGGGT	10391
rs143290272	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68604664	TCAGCCCCAATTCCT[C/T]ATCCCAGCATTCCAA	10391
rs143301326	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68707735	CCCAAGCATTAGTCT[C/T]CCAGCTTCAGGGTCA	10391
rs143303779	snp	C/T	0.0228947	0.104514	intron-variant	CORO2B	GRCh38.p7	15:68721566	CAAAAATTAGCCAGG[C/T]GTGGTGGTGCGCGCC	10391
rs143375996	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68676353	GGATTCTGAATTGAA[A/G]CAGGACTTCTGCCTC	10391
rs143381447	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674314	GGCTTCGGGACGGTG[A/G]GTAGTATATATTCTC	10391
rs143385817	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68563841	GAAACCTAAACAGCT[A/G]TAAGAAATAAAGAGA	10391
rs143389899	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68566272	TGTGAGGTGGCTGCC[A/G]TCATTATCCCCATTT	10391
rs143421432	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68557758	GTGGCAATGCCAGGA[C/T]GTAAACCCAGGCAGC	10391
rs143467968	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68606019	GTGAGCCACAGCGCC[C/T]GGCCGGCTCTTGGGT	10391
rs143473115	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68708549	TGTATTTTTTTAGTA[A/G]AGATGGGTTTCTCCG	10391
rs143494606	snp	C/T	0.0119091	0.0762411	intron-variant	CORO2B	GRCh38.p7	15:68603609	CAGGGTAAATGAGGT[C/T]ATAAAGGCAGAGCCC	10391
rs143504178	snp	A/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68693667	CCCCTTGTTCCATCC[A/G]TTTGTGGACTCACCC	10391
rs143535041	snp	G/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68561755	AGTATGCAAATATGT[G/T]CAGGGCCATGTGCCT	10391
rs143552269	snp	G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68666444	CCCAGTGTTCTGAAC[G/T]CCACAGGACCCAGGG	10391
rs143571504	snp	C/T	0.0383715	0.133092	intron-variant	CORO2B	GRCh38.p7	15:68691063	GGCCAGGTGCGGTGG[C/T]TCACGCCTGTAATCC	10391
rs143581781	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68659208	TTCCCAAAATTATTT[A/G]TATGTACATACTTAA	10391
rs143615451	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727386	CTTTCATTTCCCACT[A/G]CGCACAAAGAGTTTA	10391
rs143618934	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68655881	GTCAGTGACTCTCAG[C/G]ACTTCAAGGAACAAA	10391
rs143631243	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68587699	CATATACAATATGTT[A/T]TATATGTATTAATTC	10391
rs143645125	in-del	-/ATACACACACAC			intron-variant	CORO2B	GRCh38.p7	15:68587048	TATAGGGAGATATGT[-/ATACACACACAC]ACACACACACACACA	10391
rs143646951	snp	C/T	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68656274	GCATTCACAGCCTCA[C/T]GTGTCAAGAGACAGA	10391
rs143677717	in-del	-/TATT			intron-variant	CORO2B	GRCh38.p7	15:68721745	TGTTTTCTTGTATTT[-/TATT]ATTTATTTATGTTTT	10391
rs143688507	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68715983	GTTCCCACCTCTGCG[A/G]GTGATCCTCTTTGGA	10391
rs143706065	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585380	ACCATCATCATGATA[A/G]TAACAGTTATTAAGC	10391
rs143754104	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621433	CATTTGAACTGTACT[C/T]GTACTATTGAATAGG	10391
rs143760855	snp	A/G	1.64955e-05	0.00287184	missense	CORO2B	GRCh38.p7	15:68714562	CTTCTCCCTCAGGAG[A/G]ACCTCTCCATGCCCC	10391
rs143797826	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708214	TCTGTGGGGGGAACA[C/T]ACATGAGGGAAATGC	10391
rs143807047	snp	C/G	0.0236746	0.106192	intron-variant	CORO2B	GRCh38.p7	15:68658080	CCTGGTTCTTTGTAA[C/G]CTTGGGTGAGTTCCT	10391
rs143816613	snp	C/T	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68607715	CCCAGCTACTTGGGA[C/T]GCTGAGGTGAGAGGA	10391
rs143817037	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625181	CAGGTGCCACGCAGG[A/G]TTTAGGAATCTCTAA	10391
rs143855037	snp	G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68627387	TTATGGACCTTCAAG[G/T]GCAGGTGGGTCCCCA	10391
rs143876772	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68708700	TTTTTTATTTTCTGA[A/G]ACAGAGTCTCGCTCT	10391
rs143891009	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585533	CAGGTTGAATGAATG[A/G]GTGGGGAGCAGGGAT	10391
rs143929028	snp	A/G	0.000153988	0.00877328	missense	CORO2B	GRCh38.p7	15:68719174	GAAGACATTTACCCA[A/G]TGACACCAGGCACGG	10391
rs143937970	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68672555	AAGTGCTGGGATTAC[A/G]GACGTGAGCCAAGTA	10391
rs143964185	snp	G/T	0.0244538	0.107838	intron-variant	CORO2B	GRCh38.p7	15:68693889	CACCCAGTCTGGAGT[G/T]CAGCGGCACAATCTT	10391
rs143998257	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68604352	CGCCTTTCCTACCAC[A/G]AGCAGAACAAGTGTG	10391
rs144004715	snp	A/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68705782	TGTCAGCTCATGTAT[A/C]TAGAAGGCTTCACAC	10391
rs144066876	snp	A/G	0.0256215	0.110247	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578695	CCCCGGGCCAGCGGG[A/G]CACCCGAGAGCCCGG	10391
rs144071658	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68601960	GAGGATCACTGTGTC[A/C]CAGCATGGCGGAAGG	10391
rs144072466	snp	A/G	0.0236746	0.106192	intron-variant	CORO2B	GRCh38.p7	15:68643898	AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCCCCT	10391
rs144074008	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639980	CTTGGCCGCCCCCAC[C/T]GATTTCCCTTTGAGG	10391
rs144097837	snp	G/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68707504	CAATTAATAGAGGTC[G/T]ATTATATTCATCATG	10391
rs144105623	snp	A/T	0.0209421	0.100162	intron-variant	CORO2B	GRCh38.p7	15:68651301	GCCTGCAGGCGTGGG[A/T]CAGCCTCTAGGTTGG	10391
rs144151174	snp	C/T	0.00716266	0.059414	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615768	ACCAGACACCAAATC[C/T]GTCAGTGCCCTGGTC	10391
rs144169717	snp	C/G	0.0142736	0.0832652	intron-variant	CORO2B	GRCh38.p7	15:68712560	AACAATCCAAAATCT[C/G]AAACACTTCTGGGCC	10391
rs144218484	snp	A/G	0.0174175	0.0916809	intron-variant	CORO2B	GRCh38.p7	15:68569446	ATTTAAGGTTCCTCT[A/G]TGTGTTTTCATGACT	10391
rs144218563	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68620759	AGAGGGAGTGTGCCT[G/T]CCGTCACTCAGCCAC	10391
rs144226285	snp	C/T	0.000198564	0.00996205	synonymous-codon	CORO2B	GRCh38.p7	15:68645207	GTTCCGGAATGTCTA[C/T]GGGAAGGTGGCCAAC	10391
rs144227458	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68672709	GAACCAGGAAGAATC[C/G]TGTTCTGGGATGGAG	10391
rs144233343	in-del	-/CTGA	0.040671	0.13668	intron-variant	CORO2B	GRCh38.p7	15:68681727	ACAGAGAAAGGGGAG[-/CTGA]CTAAGTCAGGATTCC	10391
rs144287252	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68605557	GGAAAATATTCGTGC[C/T]AAGTGAAAAAGGTGG	10391
rs144322448	snp	C/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631613	AGAGCTGACACCAGG[C/G]CCCAGCTTACAGCCT	10391
rs144333758	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68668151	GAACTGGAATAAAAT[A/C]GAGTGATGCTGGCTA	10391
rs144349337	snp	A/G	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68582941	CAAAGTACCCTGAGC[A/G]GCACAATTGCCTGCT	10391
rs144349549	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68628438	GAAGGCAGTATTTGC[A/G]AAGTGCTTTGAATAG	10391
rs144413570	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68586648	AAGTCACCTGTAAAA[C/G]GTGGCCCAGTGAGGC	10391
rs144423027	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68589204	TCCCTGGTATACCAG[C/T]CAGCAGGTAAAGGCC	10391
rs144436761	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698187	TTTTACCTGGCCTGC[G/T]CGCTGCAAAGCCCAT	10391
rs144487767	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68665683	CATTTCTTGTTACAC[A/G]TATTTACCTTTTTTA	10391
rs144492201	snp	A/G	0.0111196	0.0737302	intron-variant	CORO2B	GRCh38.p7	15:68574400	CTGCCACAATGCAGC[A/G]CCCACTCACCCATGG	10391
rs144493226	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68625833	TGGTCTCAAACTCCT[A/G]AGCTCAAGCAATCTG	10391
rs144510143	snp	A/G	0.0138799	0.0821421	intron-variant	CORO2B	GRCh38.p7	15:68659750	ACCAGCCTGGCCAAC[A/G]TGGCGAAACCCCGTC	10391
rs144539309	snp	C/T	0.000214587	0.010356	synonymous-codon	CORO2B	GRCh38.p7	15:68719498	AGAAAAGAAGAGTGT[C/T]GTGGTCAACGGAATA	10391
rs144549452	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68695696	TGTCCTCTCTGAGTC[A/G]TGGTTTCTAGGAAAG	10391
rs144565082	snp	A/G	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68618787	AATTCAGGCAGTTAC[A/G]TTGTGATCTAAATAT	10391
rs144573239	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68719844	TGTCATTTGGAGTTC[C/G]AGGAGTTATAAATTC	10391
rs144616338	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68602216	GTGGGAGTGGGGGGA[A/G]CTGCTGACTGGCTTT	10391
rs144622359	snp	G/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68661510	GACTACCAGCTGGTG[G/T]TAATCTTTTCCCTTC	10391
rs144632330	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68601007	TTTAATTAAAAGGGA[A/G]AGGACACCTCCTAGC	10391
rs144633179	snp	A/G	0.000577963	0.0169896	synonymous-codon	CORO2B	GRCh38.p7	15:68711598	GATTGACTGCCACAC[A/G]GATGTGATCCTCTGC	10391
rs144641244	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669731	GTTAATAAAATAAAT[A/G]TATTTTTCTTGGAGA	10391
rs144695697	snp	C/T	3.29848e-05	0.00406095	missense	CORO2B	GRCh38.p7	15:68645295	TGTGCCGTCAACACC[C/T]GCTTCCTGGCCATCG	10391
rs144706572	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68667749	GCGGGGGGATGTGGA[A/G]GAATGCTGAAAGAGC	10391
rs144736447	snp	A/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640309	CTCTCCTCTCCTTTC[A/G/T]CATGCTTTACCAAAG	10391
rs144768135	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68596474	ATTTTGAGGCTCCAG[C/T]AGGAGCCTGCCTGCC	10391
rs144772411	snp	C/T	0.0267878	0.112589	intron-variant	CORO2B	GRCh38.p7	15:68597670	ATAAAAAAGACCAAA[C/T]GAACAAAATCCTCCA	10391
rs144837074	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721664	CTGAGTGATGGGTAC[G/T]TGGGGGTTCATGGTG	10391
rs144848505	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68691819	GCCCCTCCAGTGTAT[C/T]GCCCGTGGGCTGCTG	10391
rs144850141	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68648904	CCTAGCAATTCCACT[C/T]TAGGAATTCATCCTA	10391
rs144874326	snp	C/T	1.96292e-05	0.00313276	missense	CORO2B	GRCh38.p7	15:68710778	TGAAGCGGAACATGA[C/T]GGAGGCGCTCCTGGA	10391
rs144881558	snp	C/T	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68675225	TGTACCCCGCTTCAG[C/T]ATGCTCTGGAATTCC	10391
rs144906693	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68597641	TCAAAAAAAAAAAAA[A/T]AAATAAATAAAAAAT	10391
rs144918649	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68678172	TCCTACAACACTGGC[-/G]GGGGTTAGGACCTTT	10391
rs144941915	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577049	AATAAGAGAGCATTC[C/T]TGGCAGGCAAGCAAC	10391
rs144949304	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68576067	TGGAGGTGGGAGAAT[C/T]GCTTGAACCCGAGAG	10391
rs144953406	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68606387	GGGCATCAGCATTTA[C/T]TCCAAGCTCCCTGGA	10391
rs144967832	in-del	-/TTAA			intron-variant	CORO2B	GRCh38.p7	15:68685771	AATTGTTTGATTGAT[-/TTAA]TAAACACTTTATTTT	10391
rs144974604	snp	A/T	0.109461	0.206758	intron-variant	CORO2B	GRCh38.p7	15:68662022	AATAAATAAATAAAT[A/T]AATAAATTAATTAAT	10391
rs144983432	snp	A/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68688540	AAATCAAAATCTGAA[A/G]TACTTCTGGTCCCAA	10391
rs144987289	snp	A/G			missense	CORO2B	GRCh38.p7	15:68713956	ACCACAGAGTGAACC[A/G]GGTGGTGTTCCTGGG	10391
rs144990444	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632710	ATTCTCGTACCTCAG[C/T]CTCCTGAGTAGCTGG	10391
rs144991157	snp	A/G	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68669213	GCAAGCAAGCAAGCC[A/G]GAGACAGGACTCGGC	10391
rs145035723	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68686887	CTGCGCAACAAGAGC[A/G]AAACTCCGTCTCAAA	10391
rs145037929	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68581368	GACCAGCGTGTTCTT[A/G]TGGGGAACAGAGAGC	10391
rs145039217	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654009	CTTCCGCTTGGTGCA[A/G]TTTGCATCTCAAAGC	10391
rs145091988	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68568802	ATGGACACAGGGAGG[A/G]GAGCAACACACACTG	10391
rs145139365	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701818	TCTGAGTACCAGTTG[C/T]CCTATTGTAAAATAG	10391
rs145181094	snp	C/T	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68575694	AACCGCACTACTCCC[C/T]ACCTCCACTGCCCCA	10391
rs145272302	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595387	CAGACACCAGAGAAG[C/T]AAGGCAGCACTTCCC	10391
rs145274332	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68638352	CATCCTGGGCCAGAC[A/C]CTTTGCCAAGCAATT	10391
rs145279860	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700585	CAGGCCCTTCCCCAG[C/G]GGCTTTGGGCCCGAG	10391
rs145310801	snp	A/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68704175	ATCCTGGGAGGTGGA[A/G]GCTGCAGTGAGCCAA	10391
rs145347136	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68647849	CCTGAGACCCTGTTT[C/T]TACAAATTAAAAAAA	10391
rs145354898	snp	A/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68668771	AGAAATATGGTAACA[A/T]CACACCCCATAGAAA	10391
rs145364084	snp	A/G	0.02016	0.0983543	intron-variant	CORO2B	GRCh38.p7	15:68636744	GGAACTTCCAGGTGT[A/G]GAGGTTTGGATTGAT	10391
rs145375624	snp	G/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68621331	AGAACAACGCAGTGC[G/T]TGCCAGCATGGAGAC	10391
rs145439933	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68629716	CAGTAGGGGTCAGAT[C/T]AGGAGGACTTGGACG	10391
rs145446776	snp	C/T	0.0150606	0.0854603	intron-variant	CORO2B	GRCh38.p7	15:68707802	GTGACTACTGAGTTA[C/T]GTACTCGCCAGCTTG	10391
rs145518900	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68685727	ATGCCTGGCTCCTGC[C/T]TCTCAGATATTGGGA	10391
rs145521599	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641360	ACTCAAGAGACCACA[A/G]GTGTGCCCACCAGAG	10391
rs145530586	in-del	-/TAGAG	0.0178098	0.0926698	intron-variant	CORO2B	GRCh38.p7	15:68563198	TAATAAAGATTAGAG[-/TAGAG]ACTGGCCAGGCACCA	10391
rs145549907	snp	C/T	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68598749	CAAGGAGCTGATCTG[C/T]TAACTGGACTTTGTT	10391
rs145553137	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598300	GGTTTTAGGATTTTA[A/G]CATTGCTAAACCCTC	10391
rs145619115	snp	C/T	0.0123036	0.0774623	intron-variant	CORO2B	GRCh38.p7	15:68618141	ACATGCATACACACA[C/T]ACACACACAAATACA	10391
rs145628939	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68683257	GCCTCTGGTGGGGAG[C/T]CTGAAGGACGAAGGC	10391
rs145629907	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68609825	AGCAGCCTGTGAGCC[A/G]CGTCACTGACTGTGA	10391
rs145633603	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725101	AAGCCGGGCATGGTA[A/G]CTTACACCTGTAATC	10391
rs145640360	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68665916	TTTTATACCTCTGGT[A/G]TATCTTTCTTTTTTT	10391
rs145651536	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68571025	TTTGGAAGAAAGTGC[A/G]AAGGAAACAGAGAGG	10391
rs145674025	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68688002	CATGTTCAAGCCATA[A/G]CACCCTCCAGACCAT	10391
rs145690234	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68685757	ATTAAATTGATATTT[A/G]ATTGTTTGATTGATT	10391
rs145723342	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68685044	GAAAAAACATCTTTC[A/C]TACTGAGGCTTGGGA	10391
rs145729379	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587539	TTTTAATTTAGATTC[A/G]TTTAAGAAATACCAA	10391
rs145747154	in-del	-/ATTC	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68711004	TCTGTTCATTTGCTT[-/ATTC]ATTCATTCATTCATT	10391
rs145768070	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68696513	GAGATCGTGCCACTG[C/T]AGTCCATGCACTCCA	10391
rs145836004	snp	A/C	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68684310	GAAATGGACTAACCC[A/C]ATGTCCCCCAGTCCT	10391
rs145842063	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68653594	CCTGAAAGCCCTTAG[A/G]ACGATATTGCATGGC	10391
rs145859765	snp	C/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68610863	TTCACTGTCCCTTGA[C/G]TCCCACTCACAAAGA	10391
rs145885562	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576622	CCCTTTAAAGGTTTC[C/T]GATGGGGTCCTAGGG	10391
rs145937912	snp	C/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68662543	ATACATCAAGAACCT[C/G]AAGAGATCACTTTGT	10391
rs145948051	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68685758	TTAAATTGATATTTA[A/T]TTGTTTGATTGATTA	10391
rs145952774	snp	G/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68659229	ACATACTTAAACCTG[G/T]AAGAGTGTGAGGGAT	10391
rs145968734	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68596020	GTTTGAGTGTGGAGG[A/G]TCGGGGGCTGGGAAG	10391
rs145994534	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68712760	AGCTGGGTGCTGTTA[A/C]TCCTCTCATGTGATA	10391
rs146010395	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68608758	CCTGCCCAGACTCCC[A/G]AATGCCCTTTCTCAG	10391
rs146013169	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68626719	TCATCAAGTCCATTT[C/T]GTTGGCTGGGGAGAG	10391
rs146016935	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677800	CTCCCCTCTCCTGAT[A/T]TGTCTGTTCCTGCCT	10391
rs146090075	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571687	ACACAAAAAACATTC[A/G]CCCAAGGCACTGCAC	10391
rs146117826	snp	C/T	0.0228947	0.104514	intron-variant	CORO2B	GRCh38.p7	15:68696286	GAGCATGGTGGCACA[C/T]GCCTGTAATCCCAGC	10391
rs146133736	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68590505	ACTGGGCCATAACCC[A/G]CTGGCTGCACCGCCC	10391
rs146140711	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660359	GATGTCTGTTAGCTC[C/T]TAAGCTTCTTCAAGA	10391
rs146159879	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698491	AAACAAGACATCCAT[A/G]GTTTGTGTCCAAGAA	10391
rs146181063	in-del	-/GT	0.134119	0.221521	intron-variant	CORO2B	GRCh38.p7	15:68619754	TGAGTGCGTGCATGC[-/GT]GTGTGTGTGTGTGCA	10391
rs146213420	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631478	GCGCTAGGATTTAAA[C/T]CTGTGTCTGTCTGTG	10391
rs146229046	snp	C/T	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68661772	AGCACTTTGGGAGGC[C/T]GAGGCAAGTGGATCT	10391
rs146239121	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678538	AATTAGCCAGGTGAG[A/G]TGGTGGGTGCCTGTT	10391
rs146251749	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568212	TACCACTGACCAGCG[A/G]TATGACCCAGGACAA	10391
rs146262396	in-del	-/TT			intron-variant	CORO2B	GRCh38.p7	15:68703151	ATCTTTCTTTTTTTC[-/TT]TTTTTTTTTTTTTTT	10391
rs146279734	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68681679	GGTGTGCGTGCCCCT[C/T]GAGGGCCAGGCAGGT	10391
rs146291305	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68566888	CACATATACACAACT[C/T]GTTGGGGTTTGCCTT	10391
rs146299759	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681391	AATGCAGGGAGGGGG[A/C]CAGTGAGGAGCCCCC	10391
rs146332413	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614259	ACATGTAAGTCCCCA[A/G]TTCTGCTTCTATAGA	10391
rs146332644	snp	A/G	0.0197687	0.0974348	intron-variant	CORO2B	GRCh38.p7	15:68563690	ATCACTAATGTCAGA[A/G]ATGAAATTGGGGACA	10391
rs146375706	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68627959	CTTACTTCTGTACCC[A/G]AAATCTTCCCTCCCT	10391
rs146400609	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68662889	TAAGACAGACTAGTA[C/T]CTACAGATATTCTAT	10391
rs146417827	in-del	-/TATT	0.39325	0.204889	intron-variant	CORO2B	GRCh38.p7	15:68721744	TTAAGTGTTTTCTTG[-/TATT]GTATTTATTTATTTA	10391
rs146418130	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68638453	ATATTCAGACAGGTT[A/G]AGTAGGTAGTCCAAA	10391
rs146438326	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640951	GCAGACTCCCAGCTC[A/G]GGGTTCTGTGTGAAG	10391
rs146455643	snp	G/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68704299	CCACTATAAAACTTG[G/T]GTATGATCCCTAATT	10391
rs146499676	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707529	ATCATGGAACGGTCA[C/T]ACAACAGATGCCTCT	10391
rs146520150	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68601970	GTGTCCCAGCATGGC[A/G]GAAGGCAGAAGGCAG	10391
rs146525818	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68592613	AAAGATTCTTCCCAG[C/T]TTTCTGGTTCAAGTC	10391
rs146598423	snp	C/T	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68586748	TGATAGGGAGGGTGG[C/T]CTGACCCTGGCTGCT	10391
rs146598950	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68580272	GCCTCGGGCTTGGCC[-/G]GTCCATTCAAGGGCC	10391
rs146602627	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68653776	TTTGCTTACCCAAAG[C/T]CTTCGTTCCCATTCC	10391
rs146637769	snp	C/G	0.0142736	0.0832652	intron-variant	CORO2B	GRCh38.p7	15:68583103	TCTGCAGGCAGCCTT[C/G]CCTCTCCTGCCTCAG	10391
rs146641954	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68657557	TACAGTTATCAAAAT[A/G]TATACCAGAATTGTG	10391
rs146678597	snp	A/C/T	1.6585e-05	0.00287962	synonymous-codon, missense	CORO2B	GRCh38.p7	15:68725921	AAGGACATCCGCATT[A/C/T]GGCAGCTCCAGCTGG	10391
rs146694278	snp	C/G	0.0352966	0.128072	intron-variant	CORO2B	GRCh38.p7	15:68604414	GAGGAACCCTATTAA[C/G]AAGGGCAAAGATTGC	10391
rs146698577	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669754	CTTGGAGAAATAAAC[A/C]AAATAAGAAAAAATA	10391
rs146715895	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68564017	GCTCATTCTATAAAC[A/C]CAGCACTACCCTGAT	10391
rs146719088	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640591	AATGCAACACATGAA[C/T]CTAGGTTTCACTGAA	10391
rs146740840	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68674759	TGCCCTGATCCCAAC[A/T]ACCTTATTCCCTCTT	10391
rs146748792	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68709781	ATGATAATAATAACA[A/G]TTATAATTCCTTAGG	10391
rs146757168	snp	A/C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68561792	GCGGAGCATGTTTCC[A/C/G]TGGGTCTGAGAGTAT	10391
rs146760498	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637888	TAAAAGCTAAATTTT[C/G]CTCATGTCATCATCT	10391
rs146802525	snp	A/G	0.0279526	0.114869	intron-variant	CORO2B	GRCh38.p7	15:68658113	GCCTTTCTAGGCCTC[A/G]GTTTCCCCATCTGTA	10391
rs146818439	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724651	TCTAAAGCATTTAAT[A/T]AAGTTTTTATAGAAA	10391
rs146820737	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68654051	TGAATGTACAGTAAG[C/T]GACTTTGGAAAAGGG	10391
rs146827174	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68607176	CTGGGGTCTCTGCTA[A/G]GAAGACCTAAATGAC	10391
rs146839406	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625486	TTGCCAGCATTCATC[C/T]GTGTTCCATCTGTAG	10391
rs146904421	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68642097	GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC	10391
rs146911580	snp	A/G	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68715132	GCACAGGGGAGAGCT[A/G]TCTTCAGCTGGCTCC	10391
rs146953597	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68570579	AAGTGAGCTGATCAG[A/G]GGAACCCCAAATACG	10391
rs146990203	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587949	AGAAGACCCAGGCCT[C/G/T]GCTCTTGCCTCTGCT	10391
rs147001580	snp	A/G	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68658563	ACTTTTTCCCACCCT[A/G]ATCTATAGAATTCTG	10391
rs147035778	in-del	-/ATTC			intron-variant	CORO2B	GRCh38.p7	15:68711024	TTCATTCATTCATTC[-/ATTC]GCTACACGCAACTGA	10391
rs147071909	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68609417	AAGAGGGCTGTGGCT[-/G]GTGCAGGCTTTGGGG	10391
rs147079703	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68639480	GGTCACAGCAACCCA[A/C]CTGGGGTAGGGGAAT	10391
rs147087190	snp	A/G	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68676624	GTGCAGGTCTCAGCC[A/G]TGTTTCCCAAGTCCT	10391
rs147093384	snp	A/G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68565983	TGCTAACGAATTCCC[A/G/T]CAGCCCCATCTTTCC	10391
rs147150360	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614843	CAGCCTCTTAGTGAC[A/G]GGCCTGTTGTCCAAG	10391
rs147153977	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727931	CCCACGTCTGTACCT[A/G]CAGATATAATTTCAC	10391
rs147156120	snp	G/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68656520	AAGGTTGCACAGCTA[G/T]TTAGTGCCCCATGTG	10391
rs147170348	snp	A/G	0.0134861	0.0810011	intron-variant	CORO2B	GRCh38.p7	15:68723411	ACAGGTGTGAGCCAC[A/G]GCGCCCAGCCAATAG	10391
rs147219538	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68620004	GCAGCCTTTGCTTCC[C/T]GGGTTCAAGCAACTC	10391
rs147238591	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637103	TTCCACAGATACATG[C/T]CTTCACGACACACTC	10391
rs147255248	snp	A/C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640080	TCTGTTCCCTGCCTG[A/C/T]GCACCCATGCATCTG	10391
rs147255410	snp	A/G	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68596817	TCCACAAACCCACGG[A/G]GAGAAATGGCCGCGC	10391
rs147259558	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68706247	TTCTGCCTCCTCACC[A/G]CTTCCAACATCCCAA	10391
rs147325494	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68599961	GCATGCCCCTCCCAC[C/T]CCTTGGTGTGGACTG	10391
rs147344913	snp	A/G	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68621077	GCTTGGAGTGGACGG[A/G]TGAGATCGGCAGTGA	10391
rs147349831	in-del	-/A	0.0225045	0.103662	intron-variant	CORO2B	GRCh38.p7	15:68670240	GTGCAGTGGCGTGAT[-/A]ATTAGCTCACTGCAA	10391
rs147361419	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624548	TGGGCCTAAAACTAA[C/T]ATATGATGTATTAGT	10391
rs147367356	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690807	GGTGTGTGCCACTAT[A/G]GCTAGCTAATTTTTT	10391
rs147383865	snp	A/G	0.0955749	0.196603	intron-variant	CORO2B	GRCh38.p7	15:68686760	AAAAATTAGCTGGGC[A/G]TAGTGGCACATGCCT	10391
rs147394296	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68585231	AAACAGAGTGTCTGA[A/G]TGGAGAGATGACCAC	10391
rs147405412	in-del	-/CAAA			intron-variant	CORO2B	GRCh38.p7	15:68644043	TCAAAAACAAACAAA[-/CAAA]AAGAAAAACCAACAA	10391
rs147430613	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68580511	GACTGAATGTTTGTG[C/T]GGATTCTTGGGCCCA	10391
rs147449494	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68601091	TGGGGTGGCATGCAG[A/G]TTTTGTGGGTGTGTG	10391
rs147484943	snp	A/G	0.000181556	0.00952601	missense	CORO2B	GRCh38.p7	15:68645310	CGCTTCCTGGCCATC[A/G]TCACCGAGAGCGCAG	10391
rs147489055	snp	A/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68668455	AGAAATCCAACACAG[A/T]GATGCCGTAGAGACT	10391
rs147492952	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68575343	GAATACACCTTTTTC[-/T]TTTTTTTTTTTTTCC	10391
rs147498211	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68562853	GTGGTGGCAGGCGCC[A/G]GTAGAACCAGCTACT	10391
rs147535460	snp	C/G	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68559715	TGGGGTTCTCCCAGG[C/G]GGACTGTCGGTGAGG	10391
rs147537231	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68636331	TCTCCTTACATGTCC[A/G]GCCTTGTTCACCAGA	10391
rs147556127	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68610270	AGACAGGTTCTCTAG[C/T]GCCTCGCCTCGTTTA	10391
rs147626181	snp	A/G	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68592624	CCAGCTTTCTGGTTC[A/G]AGTCCCACCTCTCTG	10391
rs147643855	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68700616	GGAGGGCTGGGGGCC[A/G]TAACTCTCCCTGGCA	10391
rs147660276	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68592087	CCTTCCCCGGTGTCC[C/T]CAGACTCTGCAGCCA	10391
rs147662256	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68700216	GCTTGGGAGGTCAGT[C/T]GGCAAAGCTGCTGTG	10391
rs147678652	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68696914	GCAGAGCCTGGGTAC[C/T]GGTCAGATTTTCAGG	10391
rs147696108	snp	A/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68587711	GTTTTATATGTATTA[A/T]TTCATTTAAGCTTCA	10391
rs147696343	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632345	GAGCCCCACCTGGTA[G/T]GTAGCAGTGATAAAA	10391
rs147730236	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570599	CCCCAAATACGAAAG[C/T]TGAAGTGCTTACAAG	10391
rs147763841	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68569932	CACACATAACCCCTA[C/T]AGTGCACAGGCTGAT	10391
rs147766856	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68682850	CCAAATCCCAGGTGG[A/G]CTGGGCAAAAATCAC	10391
rs147780148	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68574823	GCTACATGCAGAGCT[A/G]ACACTTGAGCTGGGC	10391
rs147799943	snp	A/G	0.00716266	0.059414	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615786	CAGTGCCCTGGTCTT[A/G]GACTTCCCAACCTCC	10391
rs147823708	in-del	-/AC			intron-variant	CORO2B	GRCh38.p7	15:68602417	CTGATCACACACACA[-/AC]CACACACACACACAC	10391
rs147836662	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629758	GAAGCTAATTGAGAA[A/C]CCTGACCTCATGACT	10391
rs147873341	in-del	-/ACAC/ACACACACAC			intron-variant	CORO2B	GRCh38.p7	15:68633514	TGGTTACTCCAACAT[-/ACAC/ACACACACAC]ACACACACACACACA	10391
rs147889545	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68661603	TGCACAAAACAGTAG[A/G]GTTAGCCTACCCCTT	10391
rs147889662	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68703820	GTTTTAAAGATGAAG[C/T]TTATGCTGCATTCCA	10391
rs147905331	snp	C/T	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68598073	CCTTTTCTTCAGATC[C/T]AGACCCCCTCCACCA	10391
rs147942426	snp	C/G	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68611374	CACCCTTTGCATTGG[C/G]TGTTTTCCTTTCACT	10391
rs147959338	snp	C/G	0.0379877	0.132479	intron-variant	CORO2B	GRCh38.p7	15:68720733	AAGATGGAAGCTACA[C/G]TCTTTCTGTCACCTA	10391
rs147973532	snp	C/T	0.0364509	0.129988	intron-variant	CORO2B	GRCh38.p7	15:68659806	AGGTGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC	10391
rs147992218	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68671129	CGTGAAAATCATGCT[A/G]TTCAAGAATGTTCAA	10391
rs148010337	snp	A/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68557809	GCTAACTGGGACTCC[A/T]CAGCCTTAGTCATGG	10391
rs148024654	snp	G/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727761	GTGATTATTTATGCT[G/T]CCTCCCAAGGATAGA	10391
rs148045986	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68667513	GGACAGGGATCTTTT[C/T]GGACAGAGAAATCTT	10391
rs148064961	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630278	AGCATGAACTTGACT[A/G]TCGCTCCCTCGACCC	10391
rs148084223	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646786	CCACACAACATGTTA[A/C]GGATGTTTGGTTACT	10391
rs148113624	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68716514	CATGGCCTTACTCTC[A/G]TGGAGATCACATTCC	10391
rs148153112	snp	C/T	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68604282	AGCTCTCAGTAGCAG[C/T]TTCTACCATCAGGAA	10391
rs148154345	snp	A/G	0.0217236	0.101931	intron-variant	CORO2B	GRCh38.p7	15:68607788	GTGTTACTACACTCC[A/G]GCCTGGGTGACAGAG	10391
rs148204021	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68705310	GGGCGTGGTGGTGGG[C/T]GCCTATAATCCCAGT	10391
rs148208069	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68639276	GGGAGCCCTGAACCC[A/G]GCATGGAGTGGGGTG	10391
rs148238368	snp	A/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68689945	TTAGGAATTTAGGAG[A/T]TTTGCAAGCTGGTTG	10391
rs148242123	snp	A/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68579774	ACTCCAAAGCCACTC[A/T]GTGCAGAAGGCGCTG	10391
rs148293198	snp	A/C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68583666	CTACAGTCAGATGGC[A/C/G]AGGGGGATTATGAGG	10391
rs148311317	snp	C/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68566566	ACCCGGCGGACTCTT[C/T]ATGGTCCCAGATGCT	10391
rs148326471	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681105	GTAATCCCAGCTACT[C/T]GCGAACCTGAGGCAG	10391
rs148365588	snp	C/T	0.0150606	0.0854603	intron-variant	CORO2B	GRCh38.p7	15:68642134	CTCTGCCGTCTGGGT[C/T]CAAGCAATTCTCCTG	10391
rs148400708	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68624567	TGATGTATTAGTTGT[A/G]CATTCAAATCACCTT	10391
rs148426892	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720055	GTCCATGTCCCCCAG[C/T]GGTATTTCGTTCCAG	10391
rs148459295	snp	A/G	0.000132164	0.008128	missense	CORO2B	GRCh38.p7	15:68719508	AGTGTTGTGGTCAAC[A/G]GAATAGATTTATTAG	10391
rs148471688	snp	A/C	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68610186	TGCAGCCCTCTGGTT[A/C]CAGTGTCAGCAGCCC	10391
rs148480279	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712253	GGGGAGAGATGGAAT[A/G]GAAAATATGGATGAT	10391
rs148524549	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640450	TCATGAGACAAATCA[C/T]TGGAATGTTTTATAA	10391
rs148540653	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68601257	GCCAGGCCCTGGGAT[A/G]TAGAGATGGTTGAGA	10391
rs148551762	snp	A/C/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68663449	TAGTTGAAGAGGTAC[A/C/G]TGCTTTCTTCCAGGA	10391
rs148608255	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68585764	TTGTGTCCTGCTTAG[A/G]TTTGCCTGTGGTCTT	10391
rs148636862	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68682542	TGACATTCTCTGATC[A/G]ACTGGTAGGGACTCC	10391
rs148644582	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627423	AAAGAGTGTGTTGGT[C/G]GGGGGTGGTCAGGGA	10391
rs148679952	snp	A/C	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68569076	ACACACAATCTCCCC[A/C]ACTGTCAACATCCCC	10391
rs148681827	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68644530	TGTTCATGGCCCTAC[G/T]TAGCTGTGTAGCCTT	10391
rs148721907	snp	C/T	1.64871e-05	0.00287111	synonymous-codon	CORO2B	GRCh38.p7	15:68645255	TGGGATCCCCATCAC[C/T]AAGAATGTGCACGAC	10391
rs148725875	snp	A/C	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68673385	AAAATAAAAAATTAG[A/C]CAAGCATGCCTGAGT	10391
rs148730637	snp	A/G	0.0252325	0.109451	intron-variant	CORO2B	GRCh38.p7	15:68572758	ATTTAGATCCTAAAC[A/G]ACTGGAAGGATCTGG	10391
rs148749127	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560937	TTCTGGGTTTCCCAT[A/G]GCACAGCCCGGGTAA	10391
rs148773991	in-del	-/ATAGA	0.0295035	0.117819	intron-variant	CORO2B	GRCh38.p7	15:68675980	GAAATGGAATAGAAT[-/ATAGA]ATAGAATAGAATAAT	10391
rs148779784	snp	A/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68668210	TGAGCCTCGGTCAGC[A/G]AGAGGGCCTAGGTCA	10391
rs148795188	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68687007	CTATTGTCTTCTTCA[C/T]AGTTGTTCTGGCATT	10391
rs148804596	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631775	GATGGTCAGAGACCC[C/T]GTGGGGCCAATTCGT	10391
rs148828801	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68708072	AATTATAAAGTTTTT[C/T]GCAAGTGGGCTTTTG	10391
rs148841355	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68616648	GCGCGTGGGCCCCAG[C/T]GCAAGCAGGCAATCC	10391
rs148843579	snp	A/G	0.0189856	0.0955633	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641474	AGAGAGTGGGAGGAA[A/G]CAGAAGGAGCAGGGA	10391
rs148860000	snp	A/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68603328	ATGCACAGATGAGCG[A/C]AAGTTGGCCTGTAAC	10391
rs148865697	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68666267	CAAGTCAACAGATGA[C/T]GCTCAGATATGCAAA	10391
rs148897482	snp	A/G	0.00993419	0.0697739	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727189	TGACCACAGCCACTC[A/G]CATCCGTATAGCACT	10391
rs148909073	snp	C/G	0.0123036	0.0774623	intron-variant	CORO2B	GRCh38.p7	15:68564018	CTCATTCTATAAACC[C/G]AGCACTACCCTGATA	10391
rs148911827	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68598486	AATTTTCTCTAGAGA[A/G]TAGGCCTGCTTTCTA	10391
rs148917999	snp	A/T	0.02016	0.0983543	intron-variant	CORO2B	GRCh38.p7	15:68696550	GTGACAGAGCAAGAC[A/T]CTGCCTCAAAAAAAA	10391
rs148928528	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68587662	GCGGCTAACCCTTCC[A/G]GAGCACTTAGTTTAT	10391
rs148953559	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68658281	CTGGGGCCAGGCTGG[C/G]CAGCTCCCAATTGTT	10391
rs149000994	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646266	AGTCCCCAGAGGCCC[A/G]TGGGAGGTCACGCGC	10391
rs149039069	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68675473	GTGTCTGGAAAGAAA[C/T]GGGGACTTGAGGAGG	10391
rs149068180	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68562772	GAGGGGTCAGGAGAT[C/T]GAAACCATCCTGGCT	10391
rs149070090	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68638456	TTCAGACAGGTTGAG[G/T]AGGTAGTCCAAAGTC	10391
rs149073705	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700906	TGCTGGTGGGCCGAG[C/T]TCCACATCTTTCCTT	10391
rs149085455	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592728	GAGGCTGGTCTGTGT[A/G]CTGTACAGTATGTAC	10391
rs149090710	snp	C/T			synonymous-codon	CORO2B	GRCh38.p7	15:68725885	GATGAGATTCGACGG[C/T]TGAAAGAGGAGCTGG	10391
rs149121757	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68632838	CTCAAGTGATCTGCC[C/T]GCCTTGGTCCCCCTA	10391
rs149128094	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68661343	GGCTGAATTAGAAAC[A/G]TTGTGTTTAGGAGCA	10391
rs149138568	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625960	TATCAGTAGTTTGCT[C/T]CTTTTATTGCTGAGT	10391
rs149196691	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68680636	TCCAGACACTGGGGT[C/T]ATAGCAGAGGACAAG	10391
rs149211000	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68612891	CAGCTCCCTTGCTCC[C/T]TGTGGCTCATTTTTC	10391
rs149246949	snp	C/T	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68588936	GGAAATTTGGGATTC[C/T]GAGAAATTTGGAATT	10391
rs149267278	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68659614	AATATATTTACTATT[C/T]ATTAAGTGGAAGTGA	10391
rs149284011	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68698016	CACCAGCCAGCAGGT[A/T]GTAGCCCCTGGAACT	10391
rs149299229	snp	A/G	4.99671e-05	0.00499811	intron-variant	CORO2B	GRCh38.p7	15:68719368	GGACCATCACCTGAC[A/G]GTCCATGGGATCGTC	10391
rs149320641	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655181	TACCACAGTGCCTGG[C/T]GTACAGCAAGTGCTC	10391
rs149337304	snp	C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640233	AACCCTTGGCACTGG[C/T]CAGGTGGCCTCCTCA	10391
rs149369549	snp	A/C	0.00795532	0.062565	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578541	GGGCTCCCGGGCTTG[A/C]GGCTGCCACGCCCCT	10391
rs149417380	in-del	-/T	0.153665	0.230694	intron-variant	CORO2B	GRCh38.p7	15:68708680	CTTTGGCTTTCTTCC[-/T]TTTTTTTTTTATTTT	10391
rs149422314	snp	A/G	0.0142736	0.0832652	intron-variant	CORO2B	GRCh38.p7	15:68570895	CCTCCAGCCTCAGCC[A/G]CCCACAGTGCTGGGA	10391
rs149442963	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703062	GAACTCCTGGACTCA[A/G]GTGATCCACCCGCCT	10391
rs149444750	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68662384	AAGTGCAGGGTTTTC[A/G]TGCCTGCTGGCATAA	10391
rs149460746	snp	G/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68627370	CAGTGCCTGAGAGTG[G/T]TTTATGGACCTTCAA	10391
rs149502337	snp	C/T	0.0391387	0.134304	intron-variant	CORO2B	GRCh38.p7	15:68560096	GATGACGTGGCCGGG[C/T]ACTTGCACCCGTGCA	10391
rs149512331	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68624271	GCAGTCCCAGCTGCT[C/T]GGGAGGCTGAGGCAG	10391
rs149532286	snp	C/G	0.0279526	0.114869	intron-variant	CORO2B	GRCh38.p7	15:68688647	ATGCCACTAAATATT[C/G]TTTGAATATATGATC	10391
rs149539047	in-del	-/A	0.021333	0.101051	intron-variant	CORO2B	GRCh38.p7	15:68611087	GAGAAAATGCGCCCC[-/A]ACCACTGAGCCACTG	10391
rs149564963	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68711826	TGCATCTCACTGCAC[C/T]TCTGTTGAACAACCT	10391
rs149581487	in-del	-/TC	0.00451635	0.0473051	intron-variant	CORO2B	GRCh38.p7	15:68695112	TCAAACTAATCTCCT[-/TC]TCTCTCTCTCTCTTT	10391
rs149582238	snp	A/G	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68618348	CACATGTTGTATTAC[A/G]TGTAAATCATGTGCT	10391
rs149600731	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68605399	CAAGATGCTCATCAC[C/G]GCATTATTTATAACA	10391
rs149649944	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566193	TAGGGTCCTGTTAGA[A/T]ACCCTGTTTTACAGT	10391
rs149667412	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680499	ATGCAAATGGTACCC[C/T]CTTGAGTTGTGCAGT	10391
rs149669399	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68653538	AGGGAGAATGCAGCA[C/T]CATACAGGGGCTGCC	10391
rs149687442	snp	A/C	0.0182019	0.0936463	intron-variant	CORO2B	GRCh38.p7	15:68581924	ACGAATGCCTTAGTC[A/C]TTGTATCAGGTCCCC	10391
rs149707959	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68637643	AGATGGAAAGTGCCA[A/G]TCTTTCTCTGACAGC	10391
rs149724256	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68598129	GACTTGGCTCTGAGA[A/G]CATTTTCACTGTTTC	10391
rs149758560	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68609252	ATGGTCACCTGAAAG[A/G]GACACATTTGCTGTC	10391
rs149809956	snp	A/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68563613	AGCTGGTTATTTGAA[A/G]AGATCAACAAAAGTG	10391
rs149844360	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691727	TGTCTCCTTCCCGAG[G/T]GCAGGGCTCTGGCCA	10391
rs149847257	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587325	CTGTCCCCTGTATGA[G/T]ATAAGTGTCAACACC	10391
rs149914196	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68675213	AATTGGAATGTTTGT[A/T]CCCCGCTTCAGCATG	10391
rs149933377	snp	A/G	0.0111196	0.0737302	intron-variant	CORO2B	GRCh38.p7	15:68682068	CCGTCCCTGGATAGC[A/G]GAGGACCCTGGGTAG	10391
rs149937397	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68632427	CTTCATTTGCTAACA[C/T]GGAGAGACAGAAGTT	10391
rs149952590	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614627	GCCCCGGAGCCCTCA[C/T]GGTCAAGGATGTGTC	10391
rs149965980	snp	C/T	0.000132481	0.00813775	missense	CORO2B	GRCh38.p7	15:68695255	GCTCGGAGGACACGT[C/T]GGTGAGCAGAGGGGT	10391
rs149967519	snp	A/G	0.0248432	0.108648	intron-variant	CORO2B	GRCh38.p7	15:68669085	AGAGAGAGAGAGAGA[A/G]AGAAAGAAGGAAGGA	10391
rs149968953	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68568412	CATCATCATTTCCAT[C/T]ATCATCACTATTGCC	10391
rs149987532	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68591858	TAGGAAAACGTGGTT[A/G]TAGCATGGCGAGAAG	10391
rs150002934	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68661167	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	10391
rs150019317	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68699832	TCTCAGCCCCTCACC[A/G]GTGGCCCTGGTTCTA	10391
rs150055918	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657212	AATAGGATTACGCAA[A/G]AAGCCAATTATTTTG	10391
rs150077328	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641322	GCTGGGCTGTGGGGG[C/T]AACAGGAGATGGATA	10391
rs150085381	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68717691	TCTGCTAAGTAGCAG[A/C]AGAAGAACTCAGACC	10391
rs150095990	snp	A/G	0.00835141	0.0640778	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630901	AGCCGTGTGTGTGCC[A/G]GTATGCCAAGAAAGA	10391
rs150164962	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68588362	TTCTCTCTTCCTGTT[C/T]TGTCTATTTTGGCTG	10391
rs150209135	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68724334	TCTTTCACACAAATC[A/G]CACCTTAACTCCCAT	10391
rs150217943	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68623108	AGGCAGAGGTTGCAG[A/T]GAGCCGAGATCACGC	10391
rs150233192	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68570752	GTCAGAAGACCCCCA[G/T]GGTGCAGCAGAAAGA	10391
rs150245154	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684269	AAAAGGCTCCTGTCA[A/G]TATGTACATAGATGA	10391
rs150268949	snp	G/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68617864	CTTAGAGATTGTGGC[G/T]GAATGTGGGGGTTTG	10391
rs150277432	snp	C/G	8.42311e-05	0.0064891	synonymous-codon	CORO2B	GRCh38.p7	15:68718708	TACAGGGGTCATGCC[C/G]AAGCACGGGCTGGAT	10391
rs150278453	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671761	GCTGGCCTCCTCTGA[A/G]TGGTGATCCAGGTGA	10391
rs150285316	snp	C/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68606363	AATCATGGCCTCTGG[C/G]CTGTGGTTGGGCATC	10391
rs150301552	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562232	TATGGGGTGCAGGTG[A/G]GAAAGCCTTGAAGGA	10391
rs150402957	snp	G/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68654767	CATGGTGATGCCAAG[G/T]ACTGTTACCCATCTC	10391
rs150426365	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68584440	AGTGGCCAGCCCTGT[A/G]AGGTTGGCACACACT	10391
rs150433167	in-del	-/GT			intron-variant	CORO2B	GRCh38.p7	15:68617563	TATATGTGTGGTTGG[-/GT]GTGTGTGTGTATGCA	10391
rs150444784	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612136	TGCTCATTGTTTATC[A/G]GAGTAGATTCCCAGG	10391
rs150451920	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68660977	AATGTGTAATGAGTC[-/T]TTTTTTTTTTTCTGT	10391
rs150472530	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667995	CATGATGACAGTAAT[C/T]ACCCACACCTGTTGA	10391
rs150473431	in-del	-/C	0.0603597	0.1629	intron-variant	CORO2B	GRCh38.p7	15:68603682	GAGAGCTCACTCTCT[-/C]CGCATCTGCACAGAG	10391
rs150489301	snp	C/G	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68705428	GGGCAAAAGGTGAAA[C/G]TCTATCTCAAAAAAA	10391
rs150501226	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68581664	CTGGCAAGAAAGTCA[A/C]CTCTGATGGAGATTG	10391
rs150537549	snp	A/G	0.0551013	0.156571	intron-variant	CORO2B	GRCh38.p7	15:68624903	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAT	10391
rs150555194	snp	A/G	0.078151	0.181571	intron-variant	CORO2B	GRCh38.p7	15:68647640	GTTGTGGTGAGCTGA[A/G]ATTGTGCCATTGCAC	10391
rs150559569	snp	C/T	0.0383715	0.133092	intron-variant	CORO2B	GRCh38.p7	15:68686190	TATAGGCATGTGCCA[C/T]CACGCCTGGCTAATT	10391
rs150606304	snp	G/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68608389	CACTGTGGTCCCCTG[G/T]AGGACTTCGGCCTGA	10391
rs150622765	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68563134	TCCACACATTAAGGA[A/G]CTAGAAAAAGAAGAG	10391
rs150629432	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68663561	AGAAAGCAATAGCTA[A/T]AAAACAATCAATAAA	10391
rs150675788	snp	C/T	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68635180	CCTTCACTCCTCTCC[C/T]CACTGGTCTTGAACC	10391
rs150716557	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656827	ATGAGAGACATGCTA[A/G]TCCTAACCCCGAGGC	10391
rs150745564	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585919	AGTATGACAGAGGCA[G/T]AGCCGCCTTCTCCAT	10391
rs150763228	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68614352	CATAAAATTGTGCAT[C/T]GCTTCTTTTACGAAG	10391
rs150767672	snp	C/T	0.0763149	0.179815	intron-variant	CORO2B	GRCh38.p7	15:68722822	CCTATAATCCCAGCA[C/T]TTTGGGAGGCTGAGG	10391
rs150770067	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652208	CTTCCCCAGGTCTCT[C/T]ATTCGGGCTGCCGTT	10391
rs150802207	snp	C/G	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68707115	ACAAGCGCGCGCCAC[C/G]ACGCCCAGCTGCCGC	10391
rs150816694	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68642359	AGAGCCTGCGGTGAC[A/G]TCTGCACTGGGAAGA	10391
rs150824444	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68647873	AAAAAAAAAAAAAAG[A/G]AAAAAATTAGCCGAG	10391
rs150827765	in-del	-/CTC	0.154993	0.231244	intron-variant	CORO2B	GRCh38.p7	15:68575444	CAAGTTCAAGCAATT[-/CTC]CTGCCTCAGCCTCCT	10391
rs150835462	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631885	GAGGTGCTCCTCGCA[G/T]TCAGTGTAAATAGGC	10391
rs150838319	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68699728	ACCTCTCCTGGAGGA[C/T]GTGCTCTGGGACCCT	10391
rs150885656	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68599620	CCCCCACGCTGCCCA[A/G]ACAGATCTGGGTTGC	10391
rs150892472	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68694641	CTCCCAGAGCAGCAG[A/G]AAAGAGCCTCCTCCT	10391
rs150925990	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68720588	CATGTCCTCAGGGGC[A/T]ATTGGAGTGAGGGCC	10391
rs150936940	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68609231	TGGTGGTGGTGGTTG[-/G]GGGGGATGGTCACCT	10391
rs150941747	snp	A/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68564418	AAGCGATCCTCCCCC[A/T]TCAGCCTCTCGAGTA	10391
rs150961906	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68679190	CAAGGGAATCATCCC[A/G]TCTTATTCATCTCTA	10391
rs151010818	snp	A/G	0.00038372	0.013846	missense	CORO2B	GRCh38.p7	15:68719548	CACCCAGGACAGAGA[A/G]TGAGGTAAGGAATGT	10391
rs151015158	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68673560	GAAAGTGTCTTGGCC[A/G]GGCTCCGTGGCACAT	10391
rs151084079	snp	A/G	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68617709	TTATAGAAGATGAAA[A/G]TGGAGTCTTAAGAGG	10391
rs151137861	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68644898	TAGAAAGTGGGGTGG[A/G]CATGTGTACCAAAAG	10391
rs151154606	snp	G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68606145	CTCTACCATGTTAGG[G/T]CAAAGGTGACTGCAA	10391
rs151172496	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713122	CCAGTGGGCAGGAAA[A/G]GAGGCCCAAGACAGC	10391
rs151206104	snp	C/T	0.0260105	0.111035	intron-variant	CORO2B	GRCh38.p7	15:68701472	GCCTGCAACCACGCC[C/T]GGCTAATTTTTTTTT	10391
rs151206212	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601415	CCTTTCGGTAGGCAC[C/T]GAGGATAAAACGGTA	10391
rs151208228	snp	A/G	1.65023e-05	0.00287244	missense	CORO2B	GRCh38.p7	15:68695191	GGCCACCAGGGCAAT[A/G]TGCTGGATATCAAAT	10391
rs151209443	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668938	ACAAAATTAGCTGGG[C/T]GTGGTGGCATGTGCC	10391
rs151294876	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68687770	CTTCCTGCTATGACA[A/T]CCCATGGCAGAAGGT	10391
rs151295942	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68649602	ACTTTTGTTTATATG[C/G]GTTATATCTGTCAAT	10391
rs151306599	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68659756	TGGCCAACATGGCGA[-/A]AACCCCGTCTCTACT	10391
rs151327279	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68591279	ATGAGTAGGCAGAGG[C/T]AGATGAAGAGGCAGG	10391
rs180807622	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68717228	CTAAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG	10391
rs180817802	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68683862	GAGCATTGGAGGTGG[A/G]GGTGTATAACCATGG	10391
rs180826808	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640745	GAAATTGCCGTCCTT[C/T]GTAGGAAATGCATGC	10391
rs180833182	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68694870	ACCTTTTCCTTATTT[A/G]CAGAGGTGTATATGA	10391
rs180835246	snp	G/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68669420	GCCAGGGCCAAGGTG[G/T]GAAGTGGCTGTGAAG	10391
rs180835426	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68613489	CAAAGCTTGAAGGAC[C/G]AGTCTTCAGTCCCCT	10391
rs180841127	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624515	AGCCTGGAACTGATA[G/T]TAGGAACTACCGTCC	10391
rs180842652	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68592780	TGTGTACTGTCATGG[A/G]AGCTCAGAAGCACAG	10391
rs180856447	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68655922	GGTGCAGGAGGGGTG[A/T]GGGGAGTGGAACTAA	10391
rs180864672	snp	A/C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708584	AGCCAGGATGGTCTC[A/C/G]ATCTCCTGACCTCGT	10391
rs180881727	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601700	TGTGTGTGCGAAGGC[C/T]GGAGAAGAAATGAGG	10391
rs180894413	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562792	CCATCCTGGCTAACA[C/T]GGCGAAACCCCGTCT	10391
rs180935187	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68583562	CTCTGTGGGACACCA[C/T]CTGCCCTAGATGGAA	10391
rs181057270	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712846	AGGAGCTAGGATTCA[A/G]ACCCAGAGCCCATGC	10391
rs181061640	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662995	AAAATATTTCTAGGC[C/T]ACCTGGTTTATCGTG	10391
rs181061709	snp	C/T	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68691701	GGAGCTCATCAGTCT[C/T]TAGAAAGACTTGTCT	10391
rs181067762	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68619763	TGCATGCGTGTGTGT[A/G]TGTGCACGTGTTCAT	10391
rs181072808	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636918	CACTAGCCACATGTG[C/G]CTATTGAGCACTTGA	10391
rs181084838	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68598517	AAAAAGGACTCAACC[C/T]GAGAGAAGCCAGAAG	10391
rs181116791	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68723063	CAAGAGTGAAACTCC[A/G]TCTCAAAAAAACAAA	10391
rs181125540	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68701879	ATATAAAAGTGTTTT[A/G]TGTCCCCTAAGAACT	10391
rs181161313	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68674360	GGAAGACAGACGAGG[C/T]CATCAGAATGCCCGC	10391
rs181161682	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647996	TCACTCCCCTGCACT[C/T]CACCCTGGGCAACGG	10391
rs181166814	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608304	TGGCCAGCCCAGACC[C/T]GAACATTGGTGGTTA	10391
rs181173841	snp	A/G	0.0368353	0.130617	intron-variant	CORO2B	GRCh38.p7	15:68579366	GGGGGTGTGGGTGTG[A/G]GGAGGGGGCGCCGGT	10391
rs181175077	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68628629	AGTTACTGTACATGT[A/G]TTTTCTTTTAATCCC	10391
rs181175858	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68567679	ATACACCAATTTGGC[A/G]TATTTTCGGAAGGCA	10391
rs181191059	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68587001	AAATCTTTCTTATTA[G/T]CTATATTGGGCCTTG	10391
rs181293724	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68625802	TAGAGACGGGGTTTC[A/C]CCATGTTGCCCAGGC	10391
rs181346220	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718199	AGGAGACATAGAACA[A/G]AACAGCAATCTTAGG	10391
rs181360962	snp	C/T	0.0170251	0.090679	intron-variant	CORO2B	GRCh38.p7	15:68707112	ATTACAAGCGCGCGC[C/T]ACCACGCCCAGCTGC	10391
rs181378581	snp	A/C	0.0103295	0.0711199	intron-variant	CORO2B	GRCh38.p7	15:68653876	AAAAAAAAAAAAATG[A/C]CTGAATCTTCATCAC	10391
rs181389710	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68632839	TCAAGTGATCTGCCC[A/G]CCTTGGTCCCCCTAA	10391
rs181393133	snp	G/T	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68563684	ACTCATATCACTAAT[G/T]TCAGAAATGAAATTG	10391
rs181394699	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591851	TTCCTTCTAGGAAAA[C/T]GTGGTTATAGCATGG	10391
rs181397842	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669926	GCCAGGCATGATGGC[A/G]CATGCCTGTAATCCC	10391
rs181400770	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611878	CCAGGCTCAAGTGAT[C/T]CTCCCACCTCAGCCT	10391
rs181415754	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68625347	TTAGTGTCCACTTCT[A/G]TGCATTTCACAAATG	10391
rs181417800	snp	A/C	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68573188	CACCCCAGGGCAGGG[A/C]CCCCCAACCCCCAGC	10391
rs181510319	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68695975	GCACAGTGGGTTCAC[A/G]CCTGTAATCCCAGTG	10391
rs181517669	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641265	ACCCCGAGCCTGAGC[A/G]CTGTGGTCCCCCAGG	10391
rs181522722	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727913	GCCTTTCTGGAATGA[A/C]AACCCACGTCTGTAC	10391
rs181525952	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68602557	CCGCCTCTCCCTATC[A/G]TGTACTATGTTAAAC	10391
rs181559784	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68702314	TAATAATAATAGGTA[G/T]CACTTATTCTTTCAT	10391
rs181581552	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68648289	AGTGGGCGAGATTGC[A/G]CTACTGCACTCCAGC	10391
rs181592645	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68674780	ATTCCCTCTTTCTCC[C/T]TCCAGCCTTTCCACC	10391
rs181594225	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68629172	GTGGGGCTGCTCCAC[A/G]TTGGAAATTCTGCAG	10391
rs181607548	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608901	CCATCCATCCGTTCA[A/G]CAAGTGCTTACCAAA	10391
rs181613789	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587568	AATTTAATAGTAGTC[A/G]GTTCTCAGCCTTTCA	10391
rs181615414	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68568923	CAGCAAACCAACATG[A/G]TACACGTTTACCTAT	10391
rs181700552	snp	C/T	0.0310518	0.120672	intron-variant	CORO2B	GRCh38.p7	15:68723652	AGAGATGGGGTTTCA[C/T]CATCTTGGCCAGACT	10391
rs181723319	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636158	AATGCTTAGCTCATC[A/G]TAAGCACTAAACACA	10391
rs181751093	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68597004	GGCTCCGCAGAAGTC[C/T]TCAGGGACCGCCCTC	10391
rs181793815	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601167	GCCGCATTCTCTCCT[C/T]GCTCCTCCACACCCT	10391
rs181795794	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68682339	ACTGGAGTGCCTCAG[A/G]AAGGCTATGGGCAGG	10391
rs181807705	snp	A/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68707887	TGGTGCAGGGGTTGT[A/T]GAGGAAAGAGCATTG	10391
rs181810241	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582443	CTTCCTAGGGCAGCT[C/T]GGGGCGAGGGAGCCA	10391
rs181816005	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68561551	CTCCCTCAATCTTGC[C/T]GCAGGGAGGGAGGCA	10391
rs181932443	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68659858	AGAATCACTCGAACC[C/T]GGGAGGTGGAGGTTG	10391
rs181935467	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68617684	CAATGCTGGCATCAT[C/T]ACTCTCATTTTATAG	10391
rs181963872	snp	C/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68654389	CCTGGCTCCATTCCT[C/T]TCATTCCTTGCAGAG	10391
rs181978217	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68703214	GTCATGCAGTGGCGC[A/G]ATCTCAGCTCACTGC	10391
rs181985707	snp	C/G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68676701	GAGTGTTTAAAATGC[C/G/T]TGTTCCCAGAGGCCT	10391
rs181987996	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636740	CCCAGGAACTTCCAG[A/G]TGTGGAGGTTTGGAT	10391
rs181988963	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68723923	CTAAAAAATAAAAGT[A/C]GGCCGGGGTGGTGGC	10391
rs181989393	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68573626	TGTGGTGGGGGACAG[C/T]GGCTGGGTGACAAAA	10391
rs181992943	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68597013	GAAGTCCTCAGGGAC[C/T]GCCCTCCCCTGCCAG	10391
rs181994924	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68618236	CTGCTTCATTTTTTT[A/T]AAATACTGGTAGCAG	10391
rs182000557	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577943	ATTACCGTGGAGCAG[G/T]AAGCCAGCACTTCCG	10391
rs182003857	snp	A/C	0.0166325	0.0896639	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577644	AAGAATCGCTTGAAT[A/C]CAGGAGGCGGAGGTT	10391
rs182197383	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718494	GTGGTGAGGCAGGTC[G/T]GGCCCAAGGAGCTTG	10391
rs182206246	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68698868	GGCGCAGAGGGGCAG[A/G]GCCCACCCCACCCAC	10391
rs182211356	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574888	AAGAGGGCTAGGGCC[C/G]CAGAGGCCCAGGAAA	10391
rs182230024	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68660517	CTGGGACTTCAGGTG[C/T]GCACCACCACACCTG	10391
rs182231420	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68712219	ACCATTTTTTGAGCA[C/T]CTGCTGTGTGCTGGT	10391
rs182247076	snp	C/G	3.33195e-05	0.0040815	intron-variant	CORO2B	GRCh38.p7	15:68719376	ACCTGACAGTCCATG[C/G]GATCGTCAGTGAGAG	10391
rs182254510	snp	C/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68643553	GAGCAGGGAGACTGG[C/T]CCTGTGGGATGGAGG	10391
rs182261164	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632978	ATTTTTAAAATTACA[A/G]TGATCCCCTTTACAT	10391
rs182262844	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671114	GGAATACAACGCAGC[C/T]GTGAAAATCATGCTG	10391
rs182273902	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592546	TTAAGATTTGTGCAC[C/T]GTAGGCATGTTATAT	10391
rs182394144	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610722	TGCAGAGTAGGGTAC[C/T]CTGAGGCCCAGTCAA	10391
rs182408219	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570592	AGAGGAACCCCAAAT[A/G]CGAAAGTTGAAGTGC	10391
rs182412607	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68589228	AAAGGCCTAATGTGC[C/G]TTGTTTGCTGATTAT	10391
rs182486061	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68690983	TTTCTCAGACAACAT[A/G]TTTTCTTGGAGTTAA	10391
rs182492295	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68715719	AGCTCTGTCTGCCTG[A/G]TAGGGCAGGAAGAAG	10391
rs182495737	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68639123	CTGAAAATAAAATGC[A/T]AAACCTCAGCAGGCT	10391
rs182502200	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68668239	CATCTGCCCCACAAC[A/G]TGTTCACACTTGCAA	10391
rs182555040	snp	A/G	0.0618563	0.164627	intron-variant	CORO2B	GRCh38.p7	15:68603686	GCTCACTCTCTCCGC[A/G]TCTGCACAGAGGACA	10391
rs182573766	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68564122	GTTCTAAAACTTAGA[C/T]CATTGCTGTGCTTAT	10391
rs182608481	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708848	CAACATCTGGCTAAT[C/T]TTTTCAATTTTTTGT	10391
rs182612413	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656303	GATCTGTGACATCAG[A/C]ATCACATAGCACTTC	10391
rs182620277	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68684387	GGTCCTGAAATAGGG[C/G]ACATGAGACAAGTAA	10391
rs182623295	snp	G/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614564	AAAAGACATGGGGAC[G/T]AAGACAAGGAGAGCT	10391
rs182626390	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68634185	ACAGAGAATAGGGCT[A/G]AAAACCAGAAGTCCT	10391
rs182632126	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585818	ATGATTCGGGGAAGG[A/G]TGCTGGGGGAGGAGG	10391
rs182635309	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68564536	AGGCTGGTCTCAAAC[A/T]CCTAGGCTCAAGCGA	10391
rs182733688	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68710338	CCAAAGTGGGGCTGA[A/G]CAGAGTAGCAGGAAG	10391
rs182791826	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68621866	GGTTCAAGTGATCCT[C/T]CCACCTCAGCCTCCC	10391
rs182796476	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704712	GTATCTAATCTGTTT[C/G]GCACACAGAGGGGAG	10391
rs182804875	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68649620	TATATCTGTCAATAG[G/T]TAGCATATTCAAAAT	10391
rs182807562	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726451	AGTGATCCCTCTTTC[A/G]TCCCACCCCCTCTTC	10391
rs182821764	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68627108	CAATAATGTCAGATT[C/T]ATGAGGATAATGAGG	10391
rs182824127	snp	A/G	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68678402	GAAAAGACAGCAGGC[A/G]GTGGTTCACACCTGT	10391
rs182831804	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585450	CATGGGGTAGATTCT[A/G]TTATCCATCCCATTT	10391
rs182834956	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68650885	GTGCACTGGGTAAAG[A/T]CGAGGGGCCCCATCC	10391
rs182836355	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68705088	TGGTGCCAACTGTTT[A/G]CTATAGCCATGGGTC	10391
rs182853354	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631562	TCTCAGCCAGGAAGT[C/T]GGCAACCTTTAGACT	10391
rs182861975	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68590110	TTTCCTCAGGCCAGA[C/T]CATATCACCAGCTTG	10391
rs182863423	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610924	TAGCACCTTCCATTC[C/T]ACACCCTCGACGCAG	10391
rs182876612	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571531	CTTCACATGCACAGA[C/T]TGGAAAATAAACAAA	10391
rs183061453	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671961	GTGTGTTCTAAGGGG[A/C]AGTCAGGGGCTATCC	10391
rs183065974	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68677605	AGGTTACTTGGGAGC[A/G]GACCTTCAAAACCTC	10391
rs183073178	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720905	ACTATTTTTTGTTTT[C/G]AGACAGAGTCTCACT	10391
rs183078310	snp	C/T	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68725355	GCCTGGGCGACAAAG[C/T]GAGACTTTGTCTCAA	10391
rs183088253	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630934	TTTTCTTATGTCTCT[C/T]TCCTCTTACTGAGAC	10391
rs183104703	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68627480	AAAATTCCAGGATGC[A/G]GAGAGAAGAGGGCGG	10391
rs183248452	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625794	ATTTTTTGTAGAGAC[A/G]GGGTTTCACCATGTT	10391
rs183251578	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68670360	TTTAATTTTTTTTGG[C/T]AGAGACAGGGTTTCA	10391
rs183254649	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68642687	CATCACAGAGCAGTG[C/T]CCCACCCCCAGGATG	10391
rs183258827	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68603206	AAGTCCCAGGGCTAA[C/T]ACAGTACGTGGTCGC	10391
rs183269713	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563858	AAGAAATAAAGAGAT[A/T]CAGTAAATAATCAAG	10391
rs183270013	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68585212	CCTCTATTTAGGGAC[A/G]GATAAACAGAGTGTC	10391
rs183342438	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699989	AGGAGAGGCATCCCC[C/T]GCTGCAGCCTGGGAG	10391
rs183353353	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68643804	GCGCTTTGGGAGGCC[A/G]AGTCAGATGGATCAC	10391
rs183363701	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68605100	GTCTGGGCAACAGAG[C/T]GAGACTCCGTCTCAA	10391
rs183395485	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575192	AGAAGGTAATGCCCT[C/T]GGGTCAGCCCTCAAA	10391
rs183399773	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68691929	CAAACACTTAATGCA[C/T]ACAGCTCTGCTCAGG	10391
rs183401783	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637242	TGGCTTTCTCATTTT[A/G]CAAAGGAGGACACTG	10391
rs183428383	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68599020	CCCCATCCTTTGGCT[C/T]GGCCCTGCCCAAACC	10391
rs183460736	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68666330	CTTTCCAAGGTGTCA[C/T]GAGGTGTCAGAAGTA	10391
rs183475679	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68638288	TTTGAAGTCAGAGAC[C/T]CCCTCACAGGAGAAG	10391
rs183487162	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68599518	GCAAATTCATCAGAG[A/G]GAGCAGAATAAAGCC	10391
rs183500484	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68621131	ATAAACCCTGCCAGT[A/G]CAGGTGTAGGGACCC	10391
rs183511142	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68580415	AGATGGAGGGTTGGG[A/G]TGCAAGTGATGGAGG	10391
rs183516908	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68558666	CAAGCATGAGCCACC[A/G]CACTGGCCTCTCTCC	10391
rs183519070	snp	C/T	0.00914312	0.0669923	intron-variant	CORO2B	GRCh38.p7	15:68722849	GAGGCGGGAGGATTG[C/T]CTGAGGTTAAGAGTT	10391
rs183567053	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68673812	ACTGCACTCCAGCCT[A/G]GGCAACAGAGCGAGA	10391
rs183596633	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68714179	GAAATCAGACAGAGA[A/C]CCCCAGAGGCCGAGC	10391
rs183641628	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68665338	TATTTTCTACTTAAT[A/G]GTCTTGTTATTCATG	10391
rs183645499	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698092	TTTAGCTCTTAGAGC[C/G]ACTCCATGAGACAGG	10391
rs183656506	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68620986	ATTATATGCTGCTCC[A/G]CTTCCGGGAAGCTAT	10391
rs183657640	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657077	AACTTTAGTTTTTAA[A/C]ACTGAATAATTTTAT	10391
rs183662325	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615448	TTTCAAATATTTGTG[A/G]TGTTTCCATTCCTGA	10391
rs183665136	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68580145	TGTGCTGTGAGGGTG[A/T]TAATATGGGTCCTGG	10391
rs183697821	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68575289	GGTCTCTGGGGAACT[A/G]AGCCTCACTCCTCTG	10391
rs183729060	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635316	ACAGACCAGCCTCAG[C/T]GGCTGCAAATAGAAA	10391
rs183742647	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594925	ATCATGCTGTGTGAC[C/G]TTAGGCAAGTTGTTA	10391
rs183743937	snp	C/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616032	TTACATGCAGCGGCT[C/T]GCTCCCTCCTCCCAG	10391
rs183749243	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576473	GCCCACAACAACGGC[A/G]GATGGCGGGAAAGGT	10391
rs183869552	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68634705	GTGGGCCTCAGCAAT[C/T]TATGTTTTCACAAGC	10391
rs183872742	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68685673	TCCCAGTCTTTGCTG[A/C]TCATTGAAATCAATC	10391
rs183904225	snp	A/G	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68593600	AGCAATTCCTGGGCA[A/G]CAGTGTTAGAAAGCT	10391
rs183933422	snp	C/T	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68715060	GTGAGTCCCCTGTGG[C/T]GCACCCACTAGGAGC	10391
rs183966400	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632216	CGCTATTCATCCACA[C/T]GGCCCATCTGTGCAG	10391
rs183983089	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611545	TTTTATCTCTGTTTG[G/T]ATATATCTTCAACTG	10391
rs183989156	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591594	AGGCAGAGAGGTGAG[A/T]GGACATTCTCAAAGC	10391
rs183990785	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572397	AACCTCCTTGTCTTC[A/G]GTGGAAAGATCTAAG	10391
rs184015780	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68629656	CTGAATGTCCTTATG[A/C]AATGGTCAGGGGACC	10391
rs184030039	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68588432	GTGGTGTCCTGCTTT[A/C]ATTTGAAAAGTGAGC	10391
rs184109930	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68692325	CATATTCAGCTGGGC[A/G]CAATGGCACACGGCT	10391
rs184166165	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68610478	ACCCCCTTGTTCCAG[C/G]AACAACAGACCCCTT	10391
rs184187846	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68569305	TGTTCATCCCTCCCC[A/C]CTAACCCCTGGCCAC	10391
rs184201170	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711408	ATAGAACTCAATGAC[C/T]CCCTCCTGCACCCCA	10391
rs184204065	snp	G/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68688582	ATGGAATACTCAAAC[G/T]GTATAGAACTTGATT	10391
rs184228932	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68659536	CAGGCAACACAGTAA[A/G]AGCCCCTCTCTAAAA	10391
rs184235593	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68647933	CTTGGGAGGCTGAGG[C/T]GGGAGCATTGCTTGA	10391
rs184238059	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68616944	CAAAGGAAGAAGGGA[A/G]AGGAAGGAACTAAAG	10391
rs184246422	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636035	GAATCAGATCCCAGC[C/T]CCTCCACTTCAGTGA	10391
rs184250446	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68607202	ATGACTAGGGTGACA[A/T]CTGAGAATCATCTGG	10391
rs184260803	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687358	TCAGCTCTGCAGTGA[C/T]GGGAGAATCTAGGAA	10391
rs184291909	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68582018	CCTGGCAAGTGGAGA[A/G]GAGGAAAGCAGATGG	10391
rs184299251	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68565671	GGGATGACCCTCACT[C/T]CATGTATCAGTTGCT	10391
rs184302218	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561473	CTTCCCCTTCCAGCT[A/G]ACTGGGGCCCAGCGG	10391
rs184396027	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68658889	TTGTGAAGTGCTGTC[A/G]CTGTCCCCAGGCACA	10391
rs184399718	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68628110	TGGGGCTTTGCATAT[A/G]TTAGTAATAACAATG	10391
rs184413150	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707368	TAACTATAAAAAATA[A/T]GAAACACTTCTAGCC	10391
rs184413710	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586758	GGTGGCCTGACCCTG[A/G]CTGCTTCTAAAACTG	10391
rs184435692	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727917	TTCTGGAATGACAAC[C/T]CACGTCTGTACCTAC	10391
rs184444427	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68654094	CTCTCAAAGAGAAAA[A/G]TCGCAACTTTATTTC	10391
rs184456378	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68632872	GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC	10391
rs184468800	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68612103	AGAAGCATCCCTGAA[C/T]GAGAAATGTGTCCAC	10391
rs184492127	snp	A/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68673160	TGCCCTTCAGCAGTA[A/T]CTGAAAGGGGTGTCA	10391
rs184503958	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644461	GCTGAGAAACCTTGC[C/T]CCAAAGGGTAATCTG	10391
rs184508987	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706855	TACCTGGGACTACAG[C/G]AGCATGCCACCACAT	10391
rs184511374	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68700380	TCCCTCTACTTGTCT[C/G]AAAACATTCAGAGGA	10391
rs184520169	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68627683	GATGTAAGCAGGAAA[C/T]GGCTTCTGCCCTGAC	10391
rs184539699	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605945	TGGTCAGGCAGGTCT[A/C]AAACTCCTGAACTTG	10391
rs184547570	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68585990	GTCCAGGCCTGCAGC[C/T]CTTACGAAGCAGCCT	10391
rs184549717	snp	G/T	0.0130921	0.0798413	intron-variant	CORO2B	GRCh38.p7	15:68564794	TTCAGCCATTTTATC[G/T]GATTTTTGCAGAAGA	10391
rs184550120	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68652828	CAAGTAGCAGAGTCA[A/G]AATTTAGCCCAGGGC	10391
rs184653494	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727564	CATCCACAGAGGCCA[G/T]GGCTACCCAAGCCCC	10391
rs184672223	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68680410	AAATAAAGCAAACAA[C/T]GCAAGACAATGCTAA	10391
rs184718887	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68599837	TTGTCTAATTGTGCT[C/T]GAGGCCTGAGTGAAT	10391
rs184729276	snp	A/C	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68560453	GTGCATGCCACCATG[A/C]CCAGCTAATTAAAGA	10391
rs184730991	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727373	TTCTTTTTTCCTCCT[C/T]TCATTTCCCACTACG	10391
rs184739092	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68706314	CAACACTGCTCCTCC[A/C]AGGCCCTCCCACCCT	10391
rs184747384	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669190	AAAGAAAGAAAGGAA[A/G]CAAGCAAGCAAGCAA	10391
rs184751454	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694520	CAGGGCACTGTGTAC[C/T]GGTGTTCAAGATGTA	10391
rs184753707	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68623412	GCCCTGGCAGTGTCC[A/G]TGCATGTGGAAGCCT	10391
rs184760429	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640348	CTGATAATGGAGACA[C/T]AGTAACCTGAATCAA	10391
rs184763275	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601202	CCTTAGTGCAGCAAA[C/T]GTTTCTTGAACATTT	10391
rs184773158	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562340	CCTTCCCTTCCTCTT[A/C]TCCTGAGACTGTAGC	10391
rs184775257	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68582638	GCAGAGGACAAGGTA[C/T]ATTAATAGAGTCGTG	10391
rs184775521	snp	C/G	0.0134861	0.0810011	intron-variant	CORO2B	GRCh38.p7	15:68723212	CTGCAACCTCCACCT[C/G]CCGGGTTCAAGCAAT	10391
rs184819040	snp	A/C	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68674520	GCCTGGGTGTCTGCA[A/C]ACCTGGGTGTGGCCT	10391
rs184853006	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595564	GGGGCTTCTCCCAGG[G/T]GTGGGTTCTGTTCTC	10391
rs184895844	snp	A/C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68702141	ATCAGGTACGGGCAC[A/C/G]GGCAGGAGTGTGGAA	10391
rs184973404	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68661109	CAACCTCCCCAGTGG[C/T]TGGGATTACAGGTGC	10391
rs184980212	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577304	TTTCATTCAAGTCCT[C/T]GCTCTGTCACTGTGT	10391
rs184987794	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636742	CAGGAACTTCCAGGT[G/T]TGGAGGTTTGGATTG	10391
rs184998759	snp	A/C	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68597453	CATTCTGTGAAACTG[A/C]GGCTCCAAGGGGTTA	10391
rs185002823	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68618532	GCTGGGAGGCGTGAG[C/T]GCGCAGCTGAGGAGA	10391
rs185018418	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578135	CTGTCCCTCAAATCT[C/T]CGCAGCAGCTCCAGG	10391
rs185074411	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693912	ACAATCTTGGCTCAC[C/T]GCAACCTCCGCCTCC	10391
rs185100243	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639955	AAAGGGCCAGATTTT[C/T]AGGTCACCTCTTGGC	10391
rs185165891	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703610	GAACTTCTATACCAT[A/G]TATACAGACAGTGGG	10391
rs185176586	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68724468	AGGTATAATTTGCCT[A/G]TGGTAAAATTCATCC	10391
rs185198413	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68668845	GCACTTTGGGAGGCC[A/G]AGGTGGGTAGATCAC	10391
rs185200237	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716843	GATGTAGCAGGAGAT[G/T]GGGGGAGGATGTTAG	10391
rs185201538	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68717371	ATTTGGGAGGGGCAG[A/G]AGGAAGACAGGGAAA	10391
rs185209947	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655947	AACTAAGGTTGCCTG[G/T]CTTGAAACAGAGCAT	10391
rs185222795	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68633714	CAACTTCTCCTTTCT[C/T]ACATTTGGGGCACTG	10391
rs185228710	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622918	TATAGATACTTAGCA[C/T]GTGTCTGGTGCTTTG	10391
rs185236269	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68592932	TCTGTAACAGAATAC[C/T]GCAGACTGGGTAGTT	10391
rs185238069	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68694967	CAGCTGCAGAGCAGT[A/G]TGGCCCAGACTGACT	10391
rs185238202	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68613785	GCAAAGCTCCTACTG[C/T]GTATACCTGTATAGA	10391
rs185242476	snp	G/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68669775	AGAAAAAATAAATAA[G/T]GCTGGGTGTGGTGGC	10391
rs185255098	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574973	TACTGCAACGTCTTA[C/T]TTACCCCACAATGTG	10391
rs185336508	snp	C/G	0.00015201	0.00871677	intron-variant	CORO2B	GRCh38.p7	15:68711758	TATTGAGGGCTGGGG[C/G]TCAGCTTTCAGCAGG	10391
rs185355106	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68660080	TTACAGAAATATATC[A/G]TAATTTCTGTCTGGC	10391
rs185364781	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68617945	TACTAGATTTTTCAA[G/T]TCACTTCAGTAAATA	10391
rs185371013	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577651	GCTTGAATCCAGGAG[A/G]CGGAGGTTGCAGTGA	10391
rs185442384	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689997	AATTACATTGAGTAA[A/G]CTTGCAATTAAGTTA	10391
rs185448820	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68721899	ACTAGCGGCGTGTAC[C/G]ACCATACCCAACTAA	10391
rs185457434	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68712859	CAAACCCAGAGCCCA[C/T]GCCAAGCAGAAAGAA	10391
rs185467864	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68636330	TTCTCCTTACATGTC[C/T]GGCCTTGTTCACCAG	10391
rs185485280	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636954	GGTTAGTCTAACTGA[G/T]GAGGAGTTTTCAATT	10391
rs185487969	snp	A/C	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68691768	TAAATAGGCTCCTCT[A/C]TGTTCTGAATAGGTT	10391
rs185490183	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68663801	ATAGGCCTGTGAAAA[G/T]GTACTACTTTCCCAG	10391
rs185494325	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597005	GCTCCGCAGAAGTCC[G/T]CAGGGACCGCCCTCC	10391
rs185592014	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717043	GTGTGGTGGCTCAAG[C/G]CTGTAATCCTAGCAG	10391
rs185624504	snp	A/G	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68680097	GATGGCGGTTCTCTC[A/G]GTGGCTATCCCTAAG	10391
rs185637966	snp	A/T	0.00398564	0.0444627	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632127	CGTTATCTTGACTGC[A/T]GCAGCGGGGTCTCTG	10391
rs185651626	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68590879	AGCTTATTCTGTGTT[C/T]CTCTCCACCCTGGCT	10391
rs185752831	snp	C/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68608806	TTGAAGAGTTATGGG[C/G]CTCCAGGAGGGGAGT	10391
rs185756297	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68652511	CAGAGCTACCTGCTA[C/T]CCCAACTGGCACCTG	10391
rs185768194	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68568427	CATCATCACTATTGC[C/T]CTTTACCCTCTGAGA	10391
rs185768426	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68611065	ATCCAACCTCAGTTC[A/C]TCAACATGAGAAAAT	10391
rs185772287	snp	A/C	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68587218	AACAAACAAAAAAAA[A/C]CCCCTAAGTGTCTGC	10391
rs185790341	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68571692	AAAAACATTCGCCCA[A/G]GGCACTGCACAAGCT	10391
rs185835764	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68649510	CAGTCATTAAAATGA[A/T]GCTGTAGAGCAGTCT	10391
rs185847644	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610586	CCTCCAGCATCCTGC[A/G]CGTTTAAATTTGTAG	10391
rs185870389	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569375	ACAATGTCATCTAGT[C/T]GGAATCATGCAGTCT	10391
rs185944130	snp	A/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68676781	TTCTTCTGGATTATT[A/T]TTTTTTTTAAGACAG	10391
rs185977118	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68712233	ACCTGCTGTGTGCTG[A/G]TCATGGGGAGAGATG	10391
rs185982744	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630168	CAGCATTCAGTTGAA[C/T]AAAGAAAGAAAAAGA	10391
rs186020958	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68584153	TGAGTTCAGAGTCTC[A/G]AGGTCCAGTGGGCAT	10391
rs186026386	snp	G/T	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68563693	ACTAATGTCAGAAAT[G/T]AAATTGGGGACAATA	10391
rs186094334	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68708624	ACCTCGGCCTCCCAA[A/G]GTGCTGGGATTACAG	10391
rs186211628	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68683982	CTTATAAGGTCTAGA[G/T]AGTAGGGACCCATTG	10391
rs186218838	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703074	TCAAGTGATCCACCC[A/G]CCTCGCATCCCAAAG	10391
rs186243737	snp	A/G	0.00914312	0.0669923	intron-variant	CORO2B	GRCh38.p7	15:68648575	GAATGGTGTGAACCC[A/G]GGAGGTGGAGCTTGC	10391
rs186248403	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640810	CAAGTTCTTTTCCTG[C/T]AATTCCACAGAAGTA	10391
rs186254074	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68675048	AGAAGAAAGAGGAAC[A/T]CTTCCCCCTTCCTTT	10391
rs186256264	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68629392	CTGTTGGAGGAAGAG[A/G]CGCCTTTCTCTATTC	10391
rs186269653	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587898	CTGGTGGGAATGACC[C/T]GGAAATATGTGGTCC	10391
rs186269803	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68609578	CACATCTCTTTTGGA[A/G]TTGGGGGAGTAAATG	10391
rs186281260	snp	C/G	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68601942	CTGCATCCTCCAGAG[C/G]GGGAGGATCACTGTG	10391
rs186311772	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68562820	TCTCTACTAAAAAAT[A/G]CAAAAAATTAGCCGG	10391
rs186383237	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68628740	CTCATGACAGAGCAA[A/T]AGAGAAAGGCCTTTT	10391
rs186392942	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68598631	CGCTTGGCCTTGAAC[G/T]CCCCTCTGCAGCAGC	10391
rs186424843	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68698352	CTGGAATCACTGGCC[A/G]CCCAGGTTCCTCCTC	10391
rs186437576	snp	A/C	5.70847e-05	0.0053422	intron-variant	CORO2B	GRCh38.p7	15:68718668	CGCAGTTTCTGGGAC[A/C]CCATGGAGCCACATG	10391
rs186451351	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68670677	CAGAAGATTCACAAG[C/T]AAATAAATGCAAATA	10391
rs186451766	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68626002	CCTGTGGATGTGCCA[C/T]AGCTTTTCTTCCTGG	10391
rs186455705	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68642857	CATTCCAGGCTAGAA[C/T]TGCACAGCAAGGAAC	10391
rs186463664	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68603615	AAATGAGGTCATAAA[A/G]GCAGAGCCCTGGCCC	10391
rs186472183	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585288	CAGAGGCGGGATGCA[C/T]GCCCAGATCTTCTGG	10391
rs186580639	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68619969	CAGGCTGGAGTACAG[A/T]GGCACAGTCTTGACT	10391
rs186598917	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68696208	TGAGCTGTGATTGTG[C/T]CACTGCACTCCAGCT	10391
rs186607546	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68648082	TCACGCCTATAATCC[C/T]AGCACTTTGGGAGGC	10391
rs186632623	snp	A/G	0.0425829	0.139564	intron-variant	CORO2B	GRCh38.p7	15:68692515	GCTTGAACCCGGGAG[A/G]CGGAGGTTGCAGTGA	10391
rs186643275	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68641595	GGAACCTGGGGTAAG[C/T]GTGGACTTTGCCGGG	10391
rs186655188	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667574	CAAAGCCCCACATCT[C/G]CCTGATGGCAAAGCT	10391
rs186668712	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68638612	GGGGTAAGAGTTGAG[A/G]TGGAGAGGCTGAAGG	10391
rs186670680	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68599564	CACAAGGGCCTGAGA[C/T]GGATATAGGGAGCTT	10391
rs186682468	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559059	CACGCGCTAGGCGCC[A/G]TTCTTCCTGCTTGGG	10391
rs186684166	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580573	GGACTTGGGAGCATT[A/G]TGAGAAGATGAACTT	10391
rs186687948	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68573256	GAGGCCACGGAGAAA[A/G]GGCAAGAGAGACAAA	10391
rs186831451	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718250	TGTATGGGGAATGGC[C/G]TCTCCCTCCTTTCTC	10391
rs186863477	snp	C/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68670235	GCTGGAGTGCAGTGG[C/T]GTGATATTAGCTCAC	10391
rs186873338	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68714215	TACAGAGGCTTCAAG[A/G]AACAATGTCGGCCAC	10391
rs186876662	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68625574	GCCTGCTTGTGCACT[A/C]CGTTACAGGTTTTTT	10391
rs186877009	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68688289	ATGTTGTCACTATTA[A/G]CATTCTGATGTATTT	10391
rs186889338	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68592498	GCGGTTACATGAATG[A/C]ATACATGTATAAAAA	10391
rs186893045	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699173	CTGGGGTGGTGGTCA[A/G]TGAGAGGAGCGGGCA	10391
rs186893405	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68659261	AGGGCGCTGACCCCT[A/G]CACCATTGAAAATCC	10391
rs186904479	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68665562	AAATTAAAGAGAATG[C/T]CAACCTTATGATGTT	10391
rs186910695	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68720326	AATTCATAAGTGTCT[A/G]GCACTCTTCCTGGCT	10391
rs186910717	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635644	TGCTCTGACAGGATA[C/T]GGTTCCTTGAAAGCC	10391
rs186918189	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594934	TGTGACCTTAGGCAA[A/G]TTGTTAACCTCTCTG	10391
rs186921756	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616278	TCAGATGCACTTATT[C/T]GGGGGAAAAAGGGTT	10391
rs186938098	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576780	GGGCCTAATTTAAAT[A/T]TCCTCTGCTGCAGGT	10391
rs187021551	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630960	GAGACAAAAATCCTT[C/T]TCAGAAGCCCCCTAG	10391
rs187043828	snp	C/T	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68570988	GATGATGGCACAAAG[C/T]ACTTAATCAGGATTT	10391
rs187043920	snp	C/G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68589492	GTGGACTGCTACAGC[C/G/T]GGAAGGGACTTTAAA	10391
rs187116398	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691971	TGCAGCTTTTGCGAT[C/G]AGATGGAAGGAATGA	10391
rs187116584	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68637456	TGGAGCAGTTGATAA[C/T]GGTGTCTTTCCTTCA	10391
rs187119781	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693040	TGTAACTGATATCAA[C/T]GCTCTCCAAATCCTT	10391
rs187129195	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68716003	TCCTCTTTGGAGCTT[A/G]AGTCTAGCTTGCTTT	10391
rs187142104	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68668555	AAGTAAAGAGCATGC[A/G]GAAGAGTAGTGCCCT	10391
rs187169221	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569117	GTACATTTGTTACAA[A/T]CGATGAATCTACATT	10391
rs187186801	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68682652	CCCAGGAGGGGCAAG[A/G]ATACCATGTTTATTA	10391
rs187208917	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68633028	CATCTCTCTTCCCTC[C/T]GCTTATGGCTTCTGC	10391
rs187247937	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627493	GCAGAGAGAAGAGGG[C/T]GGGCATCTCTTTGGA	10391
rs187251600	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68592562	GTAGGCATGTTATAT[A/G]TATTTTACATCTCAA	10391
rs187258449	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68605376	AGGCGGGGAAAAACT[C/G]TATGCATCAAGATGC	10391
rs187260042	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709279	TACTCTGATTTATAA[C/T]ACTACCAACATCCAT	10391
rs187261961	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68656599	CACTCCTCCTTCCCC[C/G]ACCAAGAGAAGCACC	10391
rs187264942	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68684410	ACAAGTAAGTCTTGA[C/T]TGGGATGGAGGGAGA	10391
rs187275276	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68585819	TGATTCGGGGAAGGG[C/T]GCTGGGGGAGGAGGG	10391
rs187280723	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68564625	CCCAAAGCAGTGAAA[C/T]CTTTCTTTCTTCTGG	10391
rs187417690	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708447	CTCACTGCAAGCTCC[A/G]CCTCCCAGGCTCACA	10391
rs187426871	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654714	AAAAAGCACTTAGCA[A/C]GTAGCCTGGCCCATA	10391
rs187429776	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68613099	TCTTTCTGGAGAGGT[C/T]CAGAAGAGGCATGTA	10391
rs187440815	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68706567	TCAGTCAATGCTTAT[G/T]CACCAAGATACAGTA	10391
rs187449525	snp	A/G	0.00795532	0.062565	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726480	TCCCTCAGCAGCCCC[A/G]GAAGCCTGCCTCACC	10391
rs187469637	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68652658	TCCCCACCACAGTAG[C/T]GTGGCCTGAGGAGCT	10391
rs187470864	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68573838	CAGGAGCAGAGAAAA[C/T]GAGGCTCAGGGAGTT	10391
rs187475674	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68611188	AGTCTGGAGTAACAC[A/G]CTCCATGATTCTCTT	10391
rs187477255	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68652395	CAGCAGCCTGATTAA[A/C]CACTGGGGCCTCCCC	10391
rs187477587	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68705170	AAGTTTGGAAGATTA[A/G]CTAATACTATCTAAA	10391
rs187480963	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68678519	TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGT	10391
rs187485225	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631882	GAGGAGGTGCTCCTC[A/G]CAGTCAGTGTAAATA	10391
rs187493550	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68610989	GTACTCTGTACAAAG[C/G]TTTGTTTGTGTTAGC	10391
rs187657720	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68580156	GGTGATAATATGGGT[C/T]CTGGGTTGTGACAGG	10391
rs187663822	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68710605	CGAGCTTTGCCCATC[A/G]CCTCAAGCCAGGAGG	10391
rs187664979	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68557374	CAAGGTCATAGCAGA[A/G]CTGAGGTTCAGTGGC	10391
rs187687987	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68671181	AACCACTCTCTCCAG[C/T]TGGGCATAAAATGGA	10391
rs187688210	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727528	TACCTGCTTTTCCCA[C/T]GGCCGCCCTACGGAA	10391
rs187698189	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721945	TTTTGTAGAGACAGG[A/G]TCTTACTATATTGCA	10391
rs187702679	snp	A/G	0.000164875	0.00907801	synonymous-codon	CORO2B	GRCh38.p7	15:68715253	CGAGATCAGCACTGA[A/G]AAGCCCTACCTGAGT	10391
rs187718500	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632152	TCTCTGGGATGGTGA[C/T]GTGAGTGCCTCCTGC	10391
rs187724524	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68680205	TCTTTGCAGCTGGCA[G/T]CATGTGGCTGGGGGA	10391
rs187727406	snp	G/T	0.00993419	0.0697739	intron-variant	CORO2B	GRCh38.p7	15:68585473	TCCCATTTTCTAGAG[G/T]AGGAGAGTGAGGCTT	10391
rs187731461	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68700494	CCGTCCCCCAGGATC[C/T]GTTTCCCCTCCCTGA	10391
rs187912144	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68575423	GCTCACTGCAACCTC[C/T]GCCTCCCAAGTTCAA	10391
rs187940117	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726100	AGCCTGAGGACCCCC[A/G]CCTACCACCTCGAGA	10391
rs187956623	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68639258	TATGAGGCTCAGCTA[G/T]AAGGGAGCCCTGAAC	10391
rs187960605	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677954	TGGATTGAGGGTTTC[C/T]TGTTATTTCATGAAA	10391
rs187973296	snp	A/G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68669255	GGGAGCCCTGTTCAC[A/G/T]CCCAGACCATGGCCT	10391
rs187973485	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694549	TACACTGCAGAAGGA[C/T]GCTCATTCATATCGT	10391
rs187981840	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68624462	CGTGATCAGCACCAC[A/G]TGAGTCTGTGAAAGG	10391
rs187987328	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600091	CTCAGTGCTTCAGGG[A/T]TAAAAGATACTTGCA	10391
rs187987855	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640378	AATCAAGGCCTTAGA[C/T]CTAACTCTTAAAGTT	10391
rs187997463	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68643676	TTCCCTGGGATTCTC[C/T]TTCTGGATTCTGAAC	10391
rs187998762	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68601518	GCGTGCAGTGCGAGG[A/G]GGGCTAGGATGAGGG	10391
rs188004353	snp	C/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68561088	CCCTCCACCCCGCGT[C/G]CCCCAGGCTCCCAGC	10391
rs188011234	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68583513	CTTACCCCACTGCAT[C/T]GCCCCTTCCTGTCCT	10391
rs188024197	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68603736	TGCAAACCAGGAAGA[C/G]AGGCCTCACCAGAAA	10391
rs188030091	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68564505	TGTATTTTTAGTAGG[A/T]TTTGCCATGTTGCCC	10391
rs188209284	snp	C/T	0.0111196	0.0737302	intron-variant	CORO2B	GRCh38.p7	15:68723062	ACAAGAGTGAAACTC[C/T]GTCTCAAAAAAACAA	10391
rs188216004	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68712699	GGCCTGCACTGTGCC[C/T]GGGGCTCTGCACATC	10391
rs188222382	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661337	TCTAGAGGCTGAATT[A/T]GAAACATTGTGTTTA	10391
rs188224659	snp	A/G	0.311369	0.242351	intron-variant	CORO2B	GRCh38.p7	15:68691262	TGAACCCCGGGGGGC[A/G]GAGCTTGCAGTGAGC	10391
rs188225476	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68700128	TGAGGCATCGGCCAC[C/T]GAGGCCCTCCCTCCA	10391
rs188235921	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643991	CCAGTGAGCCGAGAT[C/T]GCACCATTGCACTCC	10391
rs188254159	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68621978	ACTATGTTGCCCAGG[C/T]TGGTATCAAACTCCT	10391
rs188257414	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614573	GGGGACTAAGACAAG[C/G]AGAGCTCCTGAATGA	10391
rs188258044	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68704718	AATCTGTTTGGCACA[C/G]AGAGGGGAGCTGGGT	10391
rs188268371	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68581333	AACCCTATCTTCTCT[C/G]CCCTTGCTGGCCCTT	10391
rs188274585	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68649758	CAAAAAAGTTAATGA[A/G]AAGAATGGCATCATT	10391
rs188456566	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717511	GACTTGCTAAGGTAT[C/T]GGATATGGAGGGGTG	10391
rs188495027	snp	C/T	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68672154	GAGCAACTTGGTAAT[C/T]GGGAGGTGTGTGTGT	10391
rs188501477	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721379	TGAGGAAAGTGGTGC[A/G]GTGTAGGTGGGTGGC	10391
rs188518183	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68590213	AGGGTACTCAGGAGC[C/T]ACAAACAAAGCTGCC	10391
rs188532071	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621007	GGGAAGCTATTACTT[C/T]CTGAAGGAGCCACAG	10391
rs188551028	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68593199	GCCCCATCTCTTAAT[A/G]CTGTTACATTGGCAA	10391
rs188629512	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68653152	GGGGTCCTGGAGCAG[C/T]GGTCCAGACAAGATA	10391
rs188644449	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68632737	CTGGGACTATAGGTG[C/T]GCGCTAGCACGCTTG	10391
rs188657083	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68591785	TGCCTGGGCTGCCAG[A/G]TGGTTCGATCTAAGG	10391
rs188663398	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611812	GATCTTACTCTGTCA[C/T]CCAGGCTGGTGTGCA	10391
rs188674864	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68573103	GCCAAGGATGCAGCC[C/T]GTAGAGGCCTCAGAC	10391
rs188766805	snp	A/G	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68686256	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	10391
rs188796264	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593777	GGTGGCGAAGTGGGT[A/G]TAGGACGCATTGCAC	10391
rs188809327	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68571558	CAAATATGTTACTAC[C/G]TCTTTTCTCCTCATT	10391
rs188813395	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68599114	AACCAGACACTGGTC[A/G]GCTTGCTGCCCCCAA	10391
rs188821970	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68563941	CCAAACATTTAAAGA[A/G]GAATCAAAACCAATT	10391
rs188880179	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689555	CCATGTGTTAGTGTT[A/G]GTGTTAGTGTATTAG	10391
rs188887270	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68628867	TCTGCTGAGAGGGAT[A/G]CCCTCAGTTTCCCAT	10391
rs188897210	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711409	TAGAACTCAATGACC[A/C]CCTCCTGCACCCCAG	10391
rs188897628	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648288	CAGTGGGCGAGATTG[C/T]GCTACTGCACTCCAG	10391
rs188907665	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68659813	GTGGTGCACGCCTGT[A/G]GTCCCAGCTACTCAG	10391
rs188919795	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68568678	CAGCCTGAGACTTGA[A/G]TGATTTTGCCCCCAT	10391
rs188919960	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68587512	TTTTAGGAATATCAC[A/G]ATGATTCCTAATTTT	10391
rs189011405	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68709545	ACACTGTAACCTCCG[C/T]GCCTGGCCTCAAGCG	10391
rs189052408	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600761	TGAGGAAATGAAAAC[A/T]GTAAATGGGACAGCC	10391
rs189052817	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68572072	GGCCCAGGGGCATCT[A/G]GGAAGGGGCTGTGGG	10391
rs189054042	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68657834	TAGATGTAAGTTGTC[G/T]CCTACCCAGACTCAC	10391
rs189060322	snp	C/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68582309	TTACTTTCTTTATAG[C/G]ATGAGAAAGAGAAGA	10391
rs189065861	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615557	TGTTGAAATCTTAAC[C/T]CCTAAAGTTATTAAG	10391
rs189074963	snp	G/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68561489	ACTGGGGCCCAGCGG[G/T]ACAGGTAGAGGGTCC	10391
rs189124370	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68707517	TCGATTATATTCATC[A/G]TGGAACGGTCATACA	10391
rs189132317	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68681723	TAAGACAGAGAAAGG[A/G]GAGCTGACTAAGTCA	10391
rs189135968	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68728213	TCTGGGTGAGACCAA[A/C]GCTCTACATTGGAAC	10391
rs189144140	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68669001	CAGAATTGCTTGAAC[C/T]TGGGAGGCAGAGGTT	10391
rs189152535	snp	A/G	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68654255	ACAAGGTTATGGGAT[A/G]GGTGTTCTCTGGATT	10391
rs189167439	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632925	AGGGGAGAGCAGGAA[G/T]GTTACACCTAGTAAA	10391
rs189269937	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68674297	GAGAGCTCCCTGCTG[G/T]GGGCTTCGGGACGGT	10391
rs189276871	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68673273	GGGCACAATGGCTCA[C/T]GTCTATGATACCAGC	10391
rs189284012	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68628460	TTTGAATAGTACCTG[A/G]CACGTAGCAAGTACA	10391
rs189286287	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68586788	GACCCAGGCAAGGGG[G/T]TGTGGAAGTGCCAAG	10391
rs189291188	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644925	AAAGCTCCTATGCCA[A/G]TCTTTGTTTTTGTAA	10391
rs189301320	snp	G/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577900	ATATATGACGTTGCC[G/T]TCGCTGTCCAGGTGA	10391
rs189303000	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627734	GACTCAGTTATTTGC[C/T]GAGCTGAATCTTGCA	10391
rs189307694	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597011	CAGAAGTCCTCAGGG[A/G]CCGCCCTCCCCTGCC	10391
rs189316060	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68562458	GAGTATAGGGCTCAT[A/G]TCTTTACATTCTTAT	10391
rs189319350	snp	A/G	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68606007	GGGATTATAGCAGTG[A/G]GCCACAGCGCCCGGC	10391
rs189330536	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68591271	CTTCCAGCATGAGTA[A/G]GCAGAGGCAGATGAA	10391
rs189504704	snp	C/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68717133	ATATGGTGAAACCCT[C/G]TCTCTAAACCCTGTC	10391
rs189510831	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641215	GCCCAGGCCCATCCC[C/T]GGGGAACACGCTGAG	10391
rs189512661	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68695843	GATAAGTAAGAGAGA[C/T]CAGGGAGGAGACAGA	10391
rs189514819	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727756	CTTCTGTGATTATTT[A/C]TGCTGCCTCCCAAGG	10391
rs189535049	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68680994	TGAGGTAGGCAGATC[A/G]CCTGAGGTCAAGAGT	10391
rs189541224	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68602394	ATTTGGTCCTGCCCA[A/C]ATTAGGGGCTGATCA	10391
rs189551246	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574867	TAGGAGTTCGCCATG[C/G]TGAGAAAGAGGGCTA	10391
rs189551540	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68647977	AGGCTGCAGTGAGCT[A/G]TGATCACTCCCCTGC	10391
rs189561871	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608184	AAACCAGACATGGGG[A/G]GCCTGAGCACGGCCA	10391
rs189584087	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68567012	GAGGTTCTCTGTTCT[C/T]TGGGTTCTGTGCTTC	10391
rs189771472	snp	G/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68669780	AAATAAATAAGGCTG[G/T]GTGTGGTGGCTCATG	10391
rs189774857	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68702231	TCCTAGCTGTGACAC[C/T]TGGGCAAGTTTTCTC	10391
rs189775388	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707000	GAGACTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	10391
rs189790251	snp	G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68619213	TGTGTTACTCTTCCA[G/T]GGAGCATTCAAGAGC	10391
rs189798610	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636819	TTTTAGGAGCTAATT[A/G]ATGTCTTTTCTCCCA	10391
rs189799001	snp	A/C	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68597919	GTGAGGACTGAGAGG[A/C]GGGCAGGATGCAGGG	10391
rs189803921	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68625295	TTAACTCGGGTTCTT[C/T]GAGGTATAATTTACA	10391
rs189804899	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570089	GAACAACAGTGCAAA[C/G]TTGCAGGGTCCACCA	10391
rs189821539	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578356	TGTGCTGTGGTCTAA[A/G]TCACTTCCCACGTCC	10391
rs189829131	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617368	CACTTTTCTGTTTAA[C/T]GTATCCTTTGTCCTC	10391
rs189862044	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577614	TAGTCCCAGATCCTC[A/G]GGGGGCTGAGGCAGA	10391
rs190009938	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68684180	GCCTTTGACTCAAAA[C/T]AGATGTCCTAGAAGT	10391
rs190026110	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68656079	TGAGAAACTTCAGGC[C/T]TGATTTAGTCCTTAG	10391
rs190028253	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708746	GTGCAGTGGTACATT[A/C]ATAGCTCACTGCAGC	10391
rs190039724	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723273	ACTACAGGTACCCAC[C/T]ACCATGCCTGGTTAA	10391
rs190048024	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593103	GCCAAACTCATTCTT[G/T]CATCAGGAGCCCACT	10391
rs190052183	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614456	TAGATGAGGAGCCTC[A/C]GGGCCAGCCAAGATT	10391
rs190059680	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68674730	CCTCACCAGGCAGGG[C/T]TGGAGTAAGAGTTTG	10391
rs190069083	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68575119	CTTTCTGCCCCAGGA[C/T]ATTCTCTGAAGCTGA	10391
rs190078489	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68668895	ACTAGCCTGACCAAC[A/G]TGCAGAAACCCCATC	10391
rs190080401	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68716874	GAGACCATCGGAGAG[C/G]GGGGCAGGGGCTAAA	10391
rs190088122	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68592499	CGGTTACATGAATGC[A/G]TACATGTATAAAAAT	10391
rs190090806	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636148	ATGAATGTAGAATGC[C/T]TAGCTCATCGTAAGC	10391
rs190110596	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68623057	GTAATCTCAGCTACT[C/G]TGGAGACTGAGGCAG	10391
rs190256241	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68678192	TTAGGACCTTTCCCA[A/C]TGAGTCTGGGAGGAC	10391
rs190260232	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68714099	ATCGTTGCCTCGGAG[A/G]TCACTTCCTCAGAAA	10391
rs190266812	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650284	GAGGCAGGAGAATTG[A/G]AGGCGGAGGTTGCGG	10391
rs190283620	snp	C/T	0.00795532	0.062565	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631061	CGTGGTGGTGCAGGG[C/T]GGTTGGGGGTAGGGG	10391
rs190296152	snp	C/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68691778	CCTCTCTGTTCTGAA[C/T]AGGTTCCGGTGATGT	10391
rs190312033	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68690186	ATTAGCCTGAAATCA[A/G]TGATCGTGGGAATAT	10391
rs190314768	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694269	AATAAGTGCTGTCAT[A/G]TATTGAGCATTTACT	10391
rs190329238	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68612500	AGTGCTCTGAGGTCT[A/G]GGGTAGAGCAGGAAA	10391
rs190339619	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636558	GCTGGGTGGCGAGGA[A/G]GAATTCCAATTTCCT	10391
rs190343215	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640153	GCAGACACCCAGCTT[C/T]GGCCCACAGTGTGTA	10391
rs190352498	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68573493	CAGAGAGCAGGGAAG[C/G]GTTGTGGTGGGTAGA	10391
rs190395016	snp	A/G	0.00795532	0.062565	intron-variant	CORO2B	GRCh38.p7	15:68564957	ATTGAAATTTCTGGA[A/G]TTTTTTTTGTGAAAT	10391
rs190510123	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709340	AACACTGGCTCTTTT[C/T]ATTTTTTTTTGGTTG	10391
rs190545254	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684483	GAGGAGCTTGTATGG[C/T]ACGTACATATGTGTG	10391
rs190575863	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660311	AGAAGCACTCATCTC[C/T]ATCAAGTTGTCTTCT	10391
rs190582249	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68711934	GTCCCCACTGCACCC[C/G]CTACCTCCAGACAGG	10391
rs190591773	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68585289	AGAGGCGGGATGCAC[A/G]CCCAGATCTTCTGGC	10391
rs190596781	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68655171	GTAAAGGTTTTACCA[C/T]AGTGCCTGGCGTACA	10391
rs190599288	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68613388	ATTAAAATGGCTTAT[C/T]AAATTAGGGTTCATC	10391
rs190612146	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68618184	AAAACAAAACCAAAG[A/G]TCATGATATGCACTC	10391
rs190628886	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68586081	TCAAACACATGGCAG[C/T]CTGTCATTTACTTGC	10391
rs190700678	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625575	CCTGCTTGTGCACTC[C/T]GTTACAGGTTTTTTT	10391
rs190710877	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603061	GGATGGGTCTGTCAA[C/T]GGTCTGTTAGGATAG	10391
rs190732823	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68585197	TGGTGGGGACGGTCC[C/T]CTCTATTTAGGGACG	10391
rs190812214	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68676987	CTGTGCTGCCCAGGC[C/T]GGTCTTGAACTCCTG	10391
rs190822572	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68724844	TGCCTTCCAGGGCTC[A/G]GCGTTTTGTGGACAT	10391
rs190832648	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630289	GACTATCGCTCCCTC[A/G]ACCCAAGTGGTCATT	10391
rs190836866	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633204	CCACCTAGAATGAGG[C/T]GGCCTCCCTTGTGAA	10391
rs190859066	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564035	GCACTACCCTGATAC[A/G]AAATCCAAACAGACA	10391
rs190866593	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588894	TGCTGACCTCCAGGT[A/G]AAAGACCAGCTTGCA	10391
rs190870308	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68592771	ATTCTGGTCTGTGTA[C/T]TGTCATGGGAGCTCA	10391
rs190942421	snp	C/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68703200	TCTGTCACCAGGCTG[C/T]CATGCAGTGGCGCGA	10391
rs190947261	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68676229	TCCAATCAGTTTAGC[A/G]TGTGTGTGCTGGCAG	10391
rs190955003	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68723797	TAAACATAAAACATG[A/C]GAGGTGTAGTGGCAC	10391
rs190959378	snp	A/G	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68648688	AGAGAGAGAAAGGAA[A/G]AAAGGCAAAAGATAT	10391
rs190962563	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68599227	AGAGCCTTCTCTGAT[C/T]TCTCCTTGCTCCAAA	10391
rs190971531	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68621074	TCAGCTTGGAGTGGA[C/T]GGATGAGATCGGCAG	10391
rs190980066	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68629613	GATGTGCAGGGAAAG[A/G]CTATGCACTGAGCAG	10391
rs190984062	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68557438	AAGGGGTCAATCTAT[A/C]CAAAGTCATAACAAG	10391
rs191076230	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704131	TGTAGTTTCAGCTAC[C/T]TGGGAGGCTGAGGTG	10391
rs191087129	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68649537	GTCTCGTTCTCCAGC[A/G]TTCAGTCTCAGGATC	10391
rs191091301	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68610588	TCCAGCATCCTGCGC[C/G]TTTAAATTTGTAGAA	10391
rs191158640	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68562901	AGAATGGCGTGAACC[C/T]GGGAGGTGGAGCTTG	10391
rs191188950	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68698526	ATAAGGCTGCATCCC[C/T]GGCCACATGAGCCAA	10391
rs191205109	snp	A/C	0.000728923	0.019077	intron-variant	CORO2B	GRCh38.p7	15:68719277	ACAGGCGGCTGCAGC[A/C]TTTGCCTTCAGCGCA	10391
rs191205203	snp	C/G/T	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68643314	GAGGGGAGAGGCTGG[C/G/T]CTGAGGTCACACAGC	10391
rs191217969	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68670885	ACAACCATTGTGAAA[A/G]GCATCTTAAAATTCA	10391
rs191219987	snp	A/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68626514	TCTCCCCTGGGCCCT[A/T]TGAGGACAAGTGATG	10391
rs191315997	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720440	AACCCACAAATGCTT[A/G]TTAGCTCACAGTTTC	10391
rs191354280	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68705004	TCGAATACTAAGGGA[C/T]TGGAATTCCTTTCCC	10391
rs191380015	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68664368	ACTGAGAGTTATTGG[C/T]GGGGCATGGTGGCTC	10391
rs191385264	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68620598	GGGAACACCTGGTCC[C/T]GCATCTTGCTTTTGA	10391
rs191386736	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68583705	CCTCCAGTTCCCTGA[C/T]GCAGAATCTAGGTAC	10391
rs191399646	snp	C/T	0.0166325	0.0896639	intron-variant	CORO2B	GRCh38.p7	15:68579485	TGCCGCTCTGGCAGC[C/T]CCGGCGGTTTGGCCA	10391
rs191437014	snp	C/T	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68692516	CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG	10391
rs191451294	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68715549	TGCCAGCATGTGCTC[A/T]GCGTCTGCACTCCTG	10391
rs191461060	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667870	GAAGACCATGGGCTT[C/T]GGGACCTGTAGTCCT	10391
rs191465288	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68621323	TTAGCTGGAGAACAA[C/T]GCAGTGCGTGCCAGC	10391
rs191471544	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572199	TTGCCCTTCCAGTCA[C/T]TGGCAGCAGCTGCAG	10391
rs191473327	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68591404	GGGCTGGAAATGGAG[A/G]GGCTGTATGTGGCTG	10391
rs191475293	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68638810	TGCCTAGTTCTGCCC[A/G]CTGGACAGCAGCGGG	10391
rs191487134	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68599788	TGCTTTCCGGACATC[A/C]GGGTCTCATTATGCT	10391
rs191554639	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726369	TGCCAGGACATCTCA[A/G]CACTCCCGCCTGGAG	10391
rs191606228	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68718265	CTCTCCCTCCTTTCT[C/G]TCTCAGGACTGGAGA	10391
rs191612373	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636955	GTTAGTCTAACTGAG[C/G]AGGAGTTTTCAATTT	10391
rs191645501	snp	A/G	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68634348	GGGTGGTTGTCAGGG[A/G]CAAACCCAAAGCACT	10391
rs191648356	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68598647	CCCCTCTGCAGCAGC[A/G]TACTCTCCCCAGCTC	10391
rs191654048	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68710656	AGAAAGCCTGGTGTC[C/T]GAGGAAAGGGGCACC	10391
rs191655835	snp	A/G	0.0298908	0.118541	intron-variant	CORO2B	GRCh38.p7	15:68670236	CTGGAGTGCAGTGGC[A/G]TGATATTAGCTCACT	10391
rs191660585	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68593343	TTTTGAAAAAGGGGA[C/T]CTGCAAATGAAATAG	10391
rs191661010	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688326	AGATTGGTTTTTTTA[C/G]ATAGGGATCCTTTTA	10391
rs191677335	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68659393	ATATACTAAATTCTC[A/G]CAATAAGTCAGCTAG	10391
rs191684468	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616279	CAGATGCACTTATTC[A/G]GGGGAAAAAGGGTTA	10391
rs191687913	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68635795	CAAGGTTTGTGATCT[C/G]GAGCTCCAACGGGAC	10391
rs191693947	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595005	CCAGTTCTAGCTGTC[C/T]GTGCAGTTCTAGCTA	10391
rs191711726	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576926	GAAAATGAGACCAGA[A/C]CCTCAGAACTAAATG	10391
rs191877775	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68610899	ACTAACACCCAGAAC[G/T]GATGGCAGGTAGCAC	10391
rs191886371	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68571491	CTGAACAAGAAAAGA[A/T]AATTCTTGGACACTG	10391
rs191894501	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68692234	TTGTTTCCAGAGTTA[A/T]AGATAACGTGCGTAA	10391
rs191897520	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68716031	TTTCCCTGTGGGTCT[A/G]GTATTATGGACAGGG	10391
rs191901352	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637593	CTGGAGAAGGAAGGC[A/G]GCTTGTCCCAGGTCA	10391
rs191910303	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68696781	GCCTCAGCTGAGCTG[C/G]TGAGGAGGGCCTGGT	10391
rs191921711	snp	C/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68656721	TCTGCATCAGCTGGC[C/T]TGGCTTTCAACCCTG	10391
rs191927432	snp	A/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615398	GCCTGGTGTAGGGCA[A/G]TCACACAGTGGATGT	10391
rs191932603	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609880	GGGGAGCACGAAGCG[G/T]TCTGGTTCAGTACAC	10391
rs191936382	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68569300	CCACCTGTTCATCCC[C/T]CCCCACTAACCCCTG	10391
rs191947756	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68642414	GAAACAGGCCTTGTG[C/T]AGACCATCCCCGGTG	10391
rs191958771	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68575216	CCTCAAACAATGGGG[A/G]AGAGGAGGGTGGATA	10391
rs192120525	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627627	GTTGGGTGAGAGGCA[C/T]TGTGACAAATGTGGT	10391
rs192130601	snp	A/C	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68708502	AGTGGCTGGGACTAC[A/C]GGTGCCTGCCACTAC	10391
rs192132726	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644371	AGTAATCAGCATTTC[C/T]TATAAATGACATAGG	10391
rs192134821	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68605862	CCTGAGTATCTGTGA[C/T]TACAGGCACCCGCCA	10391
rs192153419	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68564645	CTTTCTTCTGGTATA[A/G]TTTGTATCTTAGCGG	10391
rs192154919	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68585926	CAGAGGCAGAGCCGC[C/T]TTCTCCATTTCCATG	10391
rs192155851	snp	A/G	0.000399281	0.0141238	missense	CORO2B	GRCh38.p7	15:68711672	AGGACAAGAAGCTGC[A/G]TGTGATTGAGCCCCG	10391
rs192166774	snp	G/T	0.000379861	0.0137763	intron-variant	CORO2B	GRCh38.p7	15:68714676	AAGGTAGTAGGAGGT[G/T]GGGGAGGGCCCGGGG	10391
rs192189171	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68666170	AAAGCTGAGTGTCCT[A/C]TTTGTTTGAGGTAGA	10391
rs192244283	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68588029	GAAAATGAAGTTAGT[A/G]GTCTATCTCTGTAGG	10391
rs192296038	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727554	CGGAAAATCCCATCC[A/G]CAGAGGCCAGGGCTA	10391
rs192332538	snp	C/T	0.00398564	0.0444627	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632171	AGTGCCTCCTGCACC[C/T]GTGGCCCCCATGTGG	10391
rs192339062	snp	A/G/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68680236	GTCATTTGATCCTGA[A/G/T]TATAGACTGGCATTG	10391
rs192350253	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726712	TGACAGAACTGAGGG[C/T]TGCAATGGGGAAATG	10391
rs192375637	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68623089	AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG	10391
rs192380555	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640172	CCACAGTGTGTACTC[A/G]TGCCTGGCCTGGCCT	10391
rs192384689	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68705683	CAGTTAAGGGGCTGG[G/T]GCCTGGGCATAGACA	10391
rs192390483	snp	A/G/T	0.00199529	0.0315338	intron-variant	CORO2B	GRCh38.p7	15:68652414	TGGGGCCTCCCCAGG[A/G/T]GCACCACCCCTTTCC	10391
rs192391447	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68559967	GGGATTTAAACCTGT[G/T]TAAGGACGACTGGCG	10391
rs192394874	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679480	AGGAGGGTCTGGTCC[A/G]AGGGGCTGTGCAGAG	10391
rs192596474	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699202	CAGGAAGGGCAGCTG[C/T]GAAGGGCAGTTGGAC	10391
rs192614733	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722792	GGCAATCATGGCTGG[G/T]CACGGTGGCTCACGC	10391
rs192631219	snp	C/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68673646	AGTTCGAGACCAGCT[C/G]GCCAACATAGTGAAA	10391
rs192631994	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68643700	TCTGAACTTCTTCCT[C/T]CAATAAAGAGGAGTT	10391
rs192640296	snp	A/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604148	CCACAGGCATGAGCC[A/G/T]CCCCTCGTCGTTCTT	10391
rs192645539	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646715	AGAAATCCTCCTCTG[C/T]CTACATCTGTCATGT	10391
rs192659512	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68564535	CAGGCTGGTCTCAAA[C/T]TCCTAGGCTCAAGCG	10391
rs192692443	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68576353	AGGGATCAGAAACAT[C/T]TTCCTTCTGCCTTTG	10391
rs192698114	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68594826	CTCCAGTCCCAGGAA[A/G]GCTTTTCAGCACATA	10391
rs192705617	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68706670	CTACTCAAGTGCAGA[A/C]AAGGGTAGCCGGTAG	10391
rs192722280	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68652806	TCCTTTAAGACTGCA[C/T]GGCCCACAAGTAGCA	10391
rs192723606	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68611473	ACATGGCATCAGGAG[C/T]GTTTCCCCATTGTAT	10391
rs192751069	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68580764	AGTAATGGATGGGCC[C/T]GGCTAGAGAGAGAAA	10391
rs192773183	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668615	CAGGGCGGGGAGCCC[C/T]AGGGTGGGAAGCCAA	10391
rs192789383	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622170	GAAGGACTTAACCCA[C/T]AGCCAGGTTTGTAGT	10391
rs192793542	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68581808	GGGAGGAAATGGGTT[C/T]GAGAGTGAGCTCCCA	10391
rs192855915	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68671882	GGGGACTACACAAGG[A/C]ATGTATACTAGGAGG	10391
rs192876025	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627459	TGTGTTGGGAGAGAG[A/T]TGAGTAAAATTCCAG	10391
rs192876408	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68585482	CTAGAGGAGGAGAGT[A/G]AGGCTTAGTGAGAGT	10391
rs192892742	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68689829	AAGTAATAAATGTGC[A/C]GAGGTCAGAAGGTCT	10391
rs192910628	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68721893	GCTGGAACTAGCGGC[A/G]TGTACCACCATACCC	10391
rs192976484	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693095	CAACATACAACATCA[A/G]TGAAATTCTCCTGGG	10391
rs193003737	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600207	CATCAAATTCCAATA[C/G]CCTAAGTGCTGTTGT	10391
rs193005923	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68561458	ACTGCCTCCCAGCGC[C/T]TTCCCCTTCCAGCTA	10391
rs193039612	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68694485	GGCCTGTGGGACTCC[A/G]AAGACTATGCTTTCA	10391
rs193054608	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611050	ACAACAGCTAAGCTA[A/T]TCCAACCTCAGTTCA	10391
rs193134009	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68709773	TAATATTAATGATAA[C/T]AATAACAATTATAAT	10391
rs193138317	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658014	CTTCACTCCTGTGGG[A/G]CTCCCCAAACTCCTA	10391
rs193142115	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586686	GGCTGGTCCAGACCC[A/G]GACCTCCGGATTCTG	10391
rs193149187	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615954	AAACTTTGCCCAGAT[G/T]AGCAGGGTGGAGGAG	10391
rs193159447	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700235	AAAGCTGCTGTGTGT[A/G]CCAGGCACTGTGCTA	10391
rs193219637	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68716912	GATGCATTAGCCTGG[A/G]AAAGGAGTTTGCATT	10391
rs193220773	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68668939	CAAAATTAGCTGGGC[A/G]TGGTGGCATGTGCCT	10391
rs193231681	snp	C/T	0.00438332	0.0466095	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632038	GGGCTAGAGGGTGAC[C/T]AGCAGCCAGGCCTCC	10391
rs193232086	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68590241	GCCCCTCTGCACCAC[C/T]GCCCCCCTCTCCCAG	10391
rs193294173	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687345	CCATGTACAAAATTC[A/G]GCTCTGCAGTGATGG	10391
rs193295000	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635229	CAGACTTTGGGCTAA[C/G]GGGGTGCAAGTTGGA	10391
rs193295740	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68607106	GTTAGCAAGGGGCCT[C/T]AAGGATTTTGTGGGC	10391
rs193299551	snp	A/T	0.0189856	0.0955633	intron-variant	CORO2B	GRCh38.p7	15:68565530	TTTCAAATAAAAATA[A/T]ATATATATATATATA	10391
rs199541559	snp	A/G	8.45745e-05	0.00650231	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726011	TAAGCCGATCTCTCC[A/G]TCGTTTCTACTCATC	10391
rs199581053	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68611399	TCACTTGTTTGTTTG[-/T]TTTTTTTTCCCCTAT	10391
rs199582585	in-del	-/AAAAG			intron-variant	CORO2B	GRCh38.p7	15:68648045	AAAAAAAAAAAAAAA[-/AAAAG]AGTCTGGGCATGGTG	10391
rs199585156	snp	C/T	0.000239402	0.0109382	intron-variant	CORO2B	GRCh38.p7	15:68719584	ATTACCTCCACAGGC[C/T]CTGGAAGAGCAAGAC	10391
rs199599017	in-del	-/AGCCTGG			intron-variant	CORO2B	GRCh38.p7	15:68584807	CCTGGAGCACCCTGC[-/AGCCTGG]GGAGCTTGGGGCAGC	10391
rs199626432	in-del	-/TC			intron-variant	CORO2B	GRCh38.p7	15:68575443	CCAAGTTCAAGCAAT[-/TC]TCTGCCTCAGCCTCC	10391
rs199658404	snp	A/G	0.000725561	0.019033	synonymous-codon	CORO2B	GRCh38.p7	15:68645177	GTCCTGGCGTCCGCA[A/G]TACCGTAGCTCCAAG	10391
rs199685409	in-del	-/C	0.02016	0.0983543	intron-variant	CORO2B	GRCh38.p7	15:68625324	CATGCATTAAAAAAA[-/C]ATCTTTTTTAGTGTC	10391
rs199719205	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68721762	TTTATTTATTTATGT[A/T]TTAGAGACAGAGTCC	10391
rs199723216	snp	C/G	0.00199792	0.0315431	missense	CORO2B	GRCh38.p7	15:68725908	GGAGCTGGCCCAGAA[C/G]GACATCCGCATTCGG	10391
rs199732589	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68563500	TTTAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAA	10391
rs199736939	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68563324	AGACTACATCCCTAC[-/A]AAAAAAAACACAAAA	10391
rs199809576	in-del	-/CCCGC			intron-variant	CORO2B	GRCh38.p7	15:68691579	GCAGTGAGCCGAGAT[-/CCCGC]CACTGCACTCCAGCC	10391
rs199906350	snp	A/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640512	AAGGCAATGCTATTT[A/T]AAAAAAAAAAAAAGG	10391
rs199916811	snp	A/T	0.0267878	0.112589	intron-variant	CORO2B	GRCh38.p7	15:68697214	TGGATGGATGGATTG[A/T]TGGATGGATGGATGG	10391
rs199928997	in-del	-/C	0.0162398	0.0886349	intron-variant	CORO2B	GRCh38.p7	15:68718095	CACACTGCCCCTCAT[-/C]CCCATGATAGACGTT	10391
rs199949914	snp	A/G/T	8.79134e-05	0.0066294	intron-variant	CORO2B	GRCh38.p7	15:68710931	TTGGGGAAGAGAAAG[A/G/T]GGCCTTTTGGGTACC	10391
rs200001067	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68637746	AGTTCTCCTGGGCTC[C/T]CCCCACATTACACAG	10391
rs200147304	in-del	-/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640644	GCTGTAAAAGGCATT[-/G]GGGGGAAATTTAAAC	10391
rs200154471	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68704043	CTACACACACATACA[-/C]ACACACACACACACA	10391
rs200156309	in-del	-/TCTTTTC			intron-variant	CORO2B	GRCh38.p7	15:68690648	CACGTTAGCTTTCTT[-/TCTTTTC]TTTTTTTTTTTTTTT	10391
rs200162548	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68704288	CTAAAGTTTGACCAC[G/T]ATAAAACTTGGGTAT	10391
rs200232977	in-del	-/CTGGG	0.0182019	0.0936463	intron-variant	CORO2B	GRCh38.p7	15:68596093	GCAGGAGTGCTGTTC[-/CTGGG]CTGGGCCCATGTGTA	10391
rs200280527	in-del	-/AT			intron-variant	CORO2B	GRCh38.p7	15:68565546	TATATATATATATAT[-/AT]TTATAAAGCTCAACA	10391
rs200283131	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68691647	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGTGGTT	10391
rs200309498	in-del	-/G	0.0205511	0.0992634	intron-variant	CORO2B	GRCh38.p7	15:68674295	TGAGAGCTCCCTGCT[-/G]GGGGGCTTCGGGACG	10391
rs200387130	in-del	-/TTTTTC	0.0372196	0.131242	intron-variant	CORO2B	GRCh38.p7	15:68624681	GCATCTCTGTTTTTT[-/TTTTTC]TTTTCTTTTCTTTTT	10391
rs200414220	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68697122	TGGATGGATGGATTG[-/T]TGGATGGATGGATGG	10391
rs200485637	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68604538	GACTTTATCTCAGCA[A/G]CATGGCTAGAATATG	10391
rs200543108	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68647703	TCAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAG	10391
rs200552197	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68588391	TGTTTTAATATGCTT[A/C]GGACAAATAATCTGG	10391
rs200553647	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68662020	CAATAAATAAATAAA[-/T]TAAATAAATTAATTA	10391
rs200556372	in-del	-/CA			intron-variant	CORO2B	GRCh38.p7	15:68637750	CTCCTGGGCTCCCCC[-/CA]CATTACACAGCTGTT	10391
rs200563183	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68710947	GGCCTTTTGGGTACC[C/T]GTAGGAAGCACTGTT	10391
rs200618733	snp	C/T	0.000774763	0.0196668	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726001	GGCTGTTTTCTAAGC[C/T]GATCTCTCCGTCGTT	10391
rs200639421	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68664191	CTAAGATCTCTGTAA[-/T]TTTTTTTTTTGGATA	10391
rs200656169	in-del	-/CAG			intron-variant	CORO2B	GRCh38.p7	15:68633780	CAACGGAGCCGGCAG[-/CAG]ATCGTCCTTCTCTTC	10391
rs200677873	in-del	-/TATAG	0.0287397	0.116378	intron-variant	CORO2B	GRCh38.p7	15:68675945	GATTATAGGGTATAA[-/TATAG]TATAATAATAGAACA	10391
rs200701901	in-del	-/G	0.0146672	0.084371	intron-variant	CORO2B	GRCh38.p7	15:68627886	AGCTAACATAACTTA[-/G]ACTGAGCTTCTGGTG	10391
rs200740204	in-del	-/TTG			intron-variant	CORO2B	GRCh38.p7	15:68693850	TGTTTGTTTGTTTGT[-/TTG]TTTGAGACAGAGTCT	10391
rs200741681	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68563500	TTTAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAA	10391
rs200765147	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68683392	GCTCTGTGGCGGGGG[C/T]GGAGAAAGCCAATGC	10391
rs200786857	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68571703	CCCAAGGCACTGCAC[-/A]AGCTGAGTACAGCTG	10391
rs200802079	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68576177	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	10391
rs200817236	in-del	-/GA			intron-variant	CORO2B	GRCh38.p7	15:68669070	AGAGAGAGAGAGAGA[-/GA]AAGAAGGAAGGAAGG	10391
rs200821770	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68700807	CCAGCAGCCGCGGAG[-/AG]AGAGAGAGGTTTCTG	10391
rs200948998	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68611776	TTTCCACTTTTTTTC[-/T]TTTTTTTTTTTTTGA	10391
rs200966401	in-del	-/ATAA			intron-variant	CORO2B	GRCh38.p7	15:68665545	GATTATGTTAAATTG[-/ATAA]ATTAAAGAGAATGTC	10391
rs200966912	in-del	-/C	0.02016	0.0983543	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639682	CACCTAAATCTTGAA[-/C]CCCCCCCAGGGATGG	10391
rs201026173	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68704041	TCTACACACACATAC[-/AA]ACACACACACACACA	10391
rs201037925	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68705455	AAAAAAAAAAAAAAA[C/T]AAAGTAAATGTGCAG	10391
rs201054706	in-del	-/G	0.0209421	0.100162	intron-variant	CORO2B	GRCh38.p7	15:68560140	GGCTGGGGGCTGCCT[-/G]GGAAGATCCGGATAT	10391
rs201077689	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68703076	AGTGATCCACCCGCC[-/T]TCGCATCCCAAAGTG	10391
rs201107438	snp	A/C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629282	GTCTGCTGTGTGTGG[A/C/T]TGTCAGAGTTGTGCC	10391
rs201254383	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68653861	CTTCTCTCCCCCAGG[A/G]AAAAAAAAAAAATGC	10391
rs201290853	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68665815	CACAAATAGCTTATA[C/G]TAATTTTCAGTGGTT	10391
rs201309990	in-del	-/CAAG	0.0520825	0.152737	intron-variant	CORO2B	GRCh38.p7	15:68641821	TCCACCTTCCAGGCT[-/CAAG]CAAGCCATCCTCCCA	10391
rs201316641	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68681235	AAAAAAATTTTTTTT[G/T]GGAAAGAAAAGCTGA	10391
rs201369897	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68605133	AAAAAAAAAAAAAAA[C/T]AAGTTTTGAAAAGAA	10391
rs201411215	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68611860	CACTGCAGCCTCAAC[C/T]TCCCAGGCTCAAGTG	10391
rs201416310	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68662930	ATACCTTTTTCTTAA[-/T]TTTTTTTTTTCCTAA	10391
rs201444218	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68605656	AGACTGGAAAGTGAA[G/T]GGAGAATGGACAGGA	10391
rs201452235	in-del	-/G	0.0260105	0.111035	intron-variant	CORO2B	GRCh38.p7	15:68667785	CTATGTTTTAGTGGA[-/G]GGAGTTGCTGGAAAG	10391
rs201511457	in-del	-/ACT			intron-variant	CORO2B	GRCh38.p7	15:68670178	CAGAAGTACTTAGTG[-/ACT]GTTTGTTTTGTTTTG	10391
rs201554648	snp	G/T	0.202035	0.245356	intron-variant	CORO2B	GRCh38.p7	15:68721760	TATTTATTTATTTAT[G/T]TTTTAGAGACAGAGT	10391
rs201583566	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68563488	TGAAATTCTGTCTTT[A/T]AAAAAAAAAAAGAAA	10391
rs201619943	in-del	-/GGAT			intron-variant	CORO2B	GRCh38.p7	15:68697243	GATGGATGGATGGAT[-/GGAT]TGTTGGGTGTATGAC	10391
rs201625657	in-del	-/TC			intron-variant	CORO2B	GRCh38.p7	15:68650354	AAGAGCGAAACTCTG[-/TC]TAAAAAAAAAAAAAA	10391
rs201655545	snp	A/C/T	0.000230991	0.0107445	intron-variant	CORO2B	GRCh38.p7	15:68719134	CTCTCTTCTGCTCCT[A/C/T]CCACTGTAGTCAGAT	10391
rs201684069	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68700815	CGCGGAGAGAGAGAG[-/AG]GTTTCTGTCATCTTA	10391
rs201705107	snp	A/C/G/T	0.000117977	0.00767973	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726002	GCTGTTTTCTAAGCC[A/C/G/T]ATCTCTCCGTCGTTT	10391
rs201727592	in-del	-/A	0.021333	0.101051	intron-variant	CORO2B	GRCh38.p7	15:68661364	TTTAGGAGCAAGTTG[-/A]ACTCATGGGGTTCTG	10391
rs201758469	snp	A/C	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68623186	AAGAAAATAAAATTT[A/C]AATTAAAAAAAGATG	10391
rs201758910	in-del	-/TGG			intron-variant	CORO2B	GRCh38.p7	15:68716674	GCCTCTCTGTGATGA[-/TGG]TATTTTAAGTTGAGC	10391
rs201775824	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68684000	TAGGGACCCATTGAA[A/G]ATTTTGGAGCTGGGG	10391
rs201903698	snp	C/T	0.000826885	0.0203165	intron-variant	CORO2B	GRCh38.p7	15:68645372	GCAGGTAGGTGGCCC[C/T]TACCTTCACTCCAGC	10391
rs201925781	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68583580	GCCCTAGATGGAAGA[A/G]GCATTGCGGGAGTGG	10391
rs201936051	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68609076	GGCCCCCGGGTGCCT[C/G]CACGGTGCACTGGGT	10391
rs201945828	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68685398	GTATTTTTTAGTAAA[G/T]ATGGGATTTTGCCAT	10391
rs201951631	in-del	-/AATA			intron-variant	CORO2B	GRCh38.p7	15:68662006	GTAAGACCCTGTCTC[-/AATA]AATAAATAAATAAAT	10391
rs201980446	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68717688	TTATCTGCTAAGTAG[C/T]AGAAGAAGAACTCAG	10391
rs202006140	in-del	-/AGAA			intron-variant	CORO2B	GRCh38.p7	15:68669066	ATCAGAAAGAAAGAG[-/AGAA]AGAGAGAGAGAGAGA	10391
rs202020810	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68693828	GATCTGGTTGTGATT[G/T]GTTTGTTTGTTTGTT	10391
rs202023672	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598691	TTTAATTCTACCGCA[A/G]ACCTAGCTCTCCTCT	10391
rs202038100	in-del	-/C/TT			intron-variant	CORO2B	GRCh38.p7	15:68703153	TTTCTTTTTTTCTTT[-/C/TT]TTTTTTTTTTTTTTT	10391
rs202091370	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68629815	AGCTTGGGCTCTTAA[A/C]CAGCATGTGTGTGTG	10391
rs202092528	in-del	-/A	0.0376037	0.131863	intron-variant	CORO2B	GRCh38.p7	15:68622763	GACCAAGGCAGACAC[-/A]GGCTCTGTCCTCTCA	10391
rs202104898	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68681129	GAGGCAGGAGAATCG[C/T]TTGAACCCAGAAGGA	10391
rs202220184	in-del	-/C	0.0260105	0.111035	intron-variant	CORO2B	GRCh38.p7	15:68707943	CTCCCTCCCCCAATT[-/C]CCCCCCCTCCCACCA	10391
rs202232867	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716375	GCTTAGAGACCACAT[A/G]TGCAAGGCACCTGGC	10391
rs202244472	in-del	-/AT	0.0383715	0.133092	intron-variant	CORO2B	GRCh38.p7	15:68681226	CCATCTCAAAAAAAA[-/AT]TTTTTTTTGGAAAGA	10391
rs207475573	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68594972	TTTTTCCAATTCTGA[A/G]AAGAGTGAACTATCA	10391
rs267604301	snp	A/G			missense	CORO2B	GRCh38.p7	15:68718806	CCATGATCGTGCCCC[A/G]GAGGGTAAGTGGGGC	10391
rs367548404	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578684	TTCACCAGCGTCCCC[A/G]GGCCAGCGGGACACC	10391
rs367557673	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68690646	GATCACGTTAGCTTT[C/T]TTTTTTTTTTTTTTT	10391
rs367600905	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68672057	ACAGGAATAGTGAAC[C/T]GGGGTGAAAAGATCC	10391
rs367607399	in-del	-/AGAAA			intron-variant	CORO2B	GRCh38.p7	15:68568042	AGAAAAGAAAAGAAA[-/AGAAA]TATTGGCTATGATCA	10391
rs367612980	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68589817	GTGACCAACTAGGAG[C/T]GCCCTGACCAGAGGC	10391
rs367653470	snp	A/G	1.66471e-05	0.00288501	synonymous-codon	CORO2B	GRCh38.p7	15:68719540	AAATGTCCCACCCAG[A/G]ACAGAGAATGAGGTA	10391
rs367669461	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68664958	TACGTTTCAAATGGT[A/T]CTTTTTGCAGTGCAG	10391
rs367669962	snp	A/T	3.33217e-05	0.00408163	intron-variant	CORO2B	GRCh38.p7	15:68719370	ACCATCACCTGACAG[A/T]CCATGGGATCGTCAG	10391
rs367699827	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68698295	GATAACAGATGAGCA[G/T]TGCCTGTCTTGATGT	10391
rs367703627	snp	C/T	0.00023359	0.0108047	intron-variant	CORO2B	GRCh38.p7	15:68645146	TGACCCTTGTCTCTC[C/T]TGGCCCCTCACAGAT	10391
rs367706225	snp	C/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641500	AGGGAAAAGGAGAAG[C/G]GGGAGGGTGGACGAG	10391
rs367714969	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68610253	TAGGACTTCATAGGA[C/T]GAGACAGGTTCTCTA	10391
rs367729179	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68638562	GTTTCTTTACACTTT[G/T]GTGTAGGGCCCTGTA	10391
rs367739021	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68667982	CTGGCAGGGTTGTCA[C/T]GATGACAGTAATCAC	10391
rs367742002	snp	A/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616271	CATCACCTCAGATGC[A/T]CTTATTCGGGGGAAA	10391
rs367780401	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68584340	TTCCCCTCCCCCGAG[A/G]CACTGCCACCTTGAC	10391
rs367786874	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68681128	TGAGGCAGGAGAATC[-/G]CTTGAACCCAGAAGG	10391
rs367808997	in-del	-/TGT	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68651390	TGGCAGCGGTGGAGA[-/TGT]TGTTCCACACTAGCC	10391
rs367809136	snp	A/G	5.83675e-05	0.00540188	intron-variant	CORO2B	GRCh38.p7	15:68718654	TGATGTCACTGAGAC[A/G]CAGTTTCTGGGACCC	10391
rs367815702	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68698988	ACCAAGGTGCAGAGA[A/G]GAGAAGAGGTAGTTA	10391
rs367904807	snp	C/G/T	0.000321523	0.0126753	intron-variant	CORO2B	GRCh38.p7	15:68718825	GGTAAGTGGGGCTGG[C/G/T]CTGGGCTCCAGGAGG	10391
rs367990570	in-del	-/CT			intron-variant	CORO2B	GRCh38.p7	15:68670050	TGACAGAGCAAGACT[-/CT]GTCTCAGAAAAAAAA	10391
rs368000844	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68721625	GCAGGAGAATCACTT[A/G]AACCCAGGAGGCAGA	10391
rs368005610	snp	A/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68568806	ACACAGGGAGGGGAG[A/C]AACACACACTGGGGC	10391
rs368023348	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68624930	TCATGATACACCCAC[C/T]TTGGCCTCCCAAAGT	10391
rs368031454	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68680165	TGGTGCCATGTGACT[C/T]ACTCCCACTTCAATG	10391
rs368036298	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68619771	TGTGTGTGTGTGCAC[A/G]TGTTCATTCTCAGCA	10391
rs368066261	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68647417	GAACCCGACCGGACA[C/T]GGTGGCTCACGTCTG	10391
rs368067212	snp	C/T	0.000218427	0.0104482	intron-variant	CORO2B	GRCh38.p7	15:68711752	GGAAGGTATTGAGGG[C/T]TGGGGCTCAGCTTTC	10391
rs368067894	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68637903	GCTCATGTCATCATC[C/T]AGAAAATGCACCCGC	10391
rs368091613	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648885	AAAGATGCATGTCTA[C/T]TGACCTAGCAATTCC	10391
rs368114456	snp	A/G	0.0341408	0.126114	intron-variant	CORO2B	GRCh38.p7	15:68623558	GCCCTGCATGTAAAC[A/G]GAGGCTGGAGGACCA	10391
rs368115474	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68609244	TTGGGGGGATGGTCA[C/T]CTGAAAGGGACACAT	10391
rs368148137	snp	C/G			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68579115	CGCGCTGCCCGCCCG[C/G]AGCGCAGCCCCCAGG	10391
rs368160000	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68564307	TCATAGCAGTGAAAT[C/T]TTTTTTTTTTTTTTG	10391
rs368187900	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68571170	TTTCTTTGTTAGTTT[C/G]TGAGGAATTTCCCTG	10391
rs368255810	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68574051	CTGTTGGACTTCAAC[-/C]TGAGGACACCAGGGA	10391
rs368297235	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68558369	AAACTCCCTTCCCCC[-/C]TCACCATTTTTTTTT	10391
rs368298490	snp	G/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68649455	CATTAAGGAAATGGG[G/T]TAAACAAATTAGGGA	10391
rs368301131	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726186	TGGAGACCCCCTGCC[A/G]GCAGCCCCTTTCCCT	10391
rs368336431	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68567190	CCCTTCGGCTCTCAG[C/T]GGGCTCTTTGCCTGG	10391
rs368342006	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68696113	AAACTAGGTGGGTGT[G/T]GTGGTGCACACCTGT	10391
rs368352593	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68676088	GTGGTCAGGGAATCT[C/G]ATAGGCTCAGCTTGA	10391
rs368354157	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68605316	TCCATATCCTGTGAC[C/G]TAGTAATCCCGCTTC	10391
rs368356205	snp	A/C/G	0.000199858	0.00999482	intron-variant	CORO2B	GRCh38.p7	15:68719381	ACAGTCCATGGGATC[A/C/G]TCAGTGAGAGCGTTT	10391
rs368357685	snp	C/G/T	0.000132665	0.0081436	intron-variant	CORO2B	GRCh38.p7	15:68715323	CTAGGTAAGTGGCCC[C/G/T]GAGGCTGCCACAGCT	10391
rs368365854	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68684280	GTCAATATGTACATA[C/G]ATGACCCGCAAGGAG	10391
rs368451563	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68646497	GGGGAGCACAGATTT[A/G]GAAAAGGCTTAGACC	10391
rs368467837	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68619014	GAGAGGCAAGGATAC[C/T]TGTCAGAAGATGGTA	10391
rs368489169	snp	A/G/T	0.000232858	0.0107878	intron-variant	CORO2B	GRCh38.p7	15:68711538	CATGCATCTGCCCTC[A/G/T]CAGGTCCTCATCTGG	10391
rs368503992	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68686514	AGAGCTCAGTGTCTC[A/G]TCCATAAAATGAACT	10391
rs368523459	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68704662	TGCCTCCCCAACAAG[A/T]CTGACAGCTACTTGA	10391
rs368532758	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68691607	TCCAGCCTGGGCGAC[-/AG]AGCGAGACTCCGTCT	10391
rs368543604	in-del	-/AAGC			intron-variant	CORO2B	GRCh38.p7	15:68669187	GAAAAGAAAGAAAGG[-/AAGC]AAGCAAGCAAGCAAG	10391
rs368549249	in-del	-/GA			intron-variant	CORO2B	GRCh38.p7	15:68648668	AAAAAGAAAGAGAGA[-/GA]AAGAGAGAGAGAAAG	10391
rs368558576	snp	C/T	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68675613	AGGGAAATGATAACT[C/T]CTCCACAGAGGTAGT	10391
rs368562338	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68613176	AACACTTTATCGCAT[C/G]ACCACATACTAGGTT	10391
rs368616326	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630233	GCTGGACCCAGGGGA[C/T]GCTGTGTGGGGTGGT	10391
rs368682108	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68717267	TGCGGTGAGCTAAGA[G/T]CACACCACTGCACTC	10391
rs368685487	snp	C/T			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632160	ATGGTGATGTGAGTG[C/T]CTCCTGCACCCGTGG	10391
rs368731773	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68634706	GGGCCTCAGCAATCT[-/A]ATGTTTTCACAAGCC	10391
rs368740754	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68701744	CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC	10391
rs368753070	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68638077	AATACTTTTTCCTTC[C/T]GGGCCCTCCCCATCT	10391
rs368791941	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702809	AAACCATATCTTTTT[C/T]TTTTTCTTTTTCTTT	10391
rs368798830	in-del	-/GT/TG			intron-variant	CORO2B	GRCh38.p7	15:68619755	GCGTGTGTGTGTGTG[-/GT/TG]CACGTGTTCATTCTC	10391
rs368806737	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68619614	ACACAAGATAGTCCC[A/G]GCAGGGCCTGAATAA	10391
rs368813338	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68557891	TGCCAGCATTACACA[A/G]CATGAGGTCCTGGTC	10391
rs368836689	snp	A/G	0.0126979	0.078662	intron-variant	CORO2B	GRCh38.p7	15:68560016	AATGCAGATCTGACC[A/G]AGTCTCTGCCAGCCC	10391
rs368878346	snp	C/T	1.66513e-05	0.00288537	intron-variant	CORO2B	GRCh38.p7	15:68725805	CTCACCTGCTCTCTC[C/T]TGGGCCCTCCTTGGC	10391
rs368901738	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68707820	ACTCGCCAGCTTGTT[C/T]CCCCTGCACCCTCTC	10391
rs368924940	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68672607	TTAAAACAGAAATGT[C/T]TGAGGACAGTGAATT	10391
rs368937981	snp	C/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615377	CCTCTCTGTGTAACC[C/T]GGGGGGCCTGGTGTA	10391
rs368941537	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68643145	TAAAGCAATTTAAAA[C/T]AAACACATGACTGGC	10391
rs368951496	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68582072	ACTTCTGTAGAGGAG[A/G]TGAGCCTGTTTTCCA	10391
rs368967612	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68702068	GCCAACATGATAAGC[A/G]GAAGGACAGATCATG	10391
rs368989891	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68681843	GCAGAGATAACACAG[A/T]TGTAGTTATCTGTTG	10391
rs369018433	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68585931	GCAGAGCCGCCTTCT[C/T]CATTTCCATGAGGCT	10391
rs369021369	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68722614	GACCAAAAAACAATG[C/T]AAAGAAATTTTGAGA	10391
rs369047377	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658459	GCCAGATAACAACCT[A/G]GGTAGAAGCGGGAGG	10391
rs369056285	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68696628	CACTCCTTCCTCAGA[C/G]TCTACCAACTTTCAC	10391
rs369091904	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68673613	GAGGCCAAGGCAGGC[A/G]AATCACTTAAGGTCA	10391
rs369095050	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68713602	TCTTCTGGGGGTTGC[C/T]GGCTCCCGTGGCTGG	10391
rs369097056	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68709831	TTTATAAACTGTTAT[A/T]CCATTGTGTCTTTTC	10391
rs369124564	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68655254	GTTGGTGGGAGAAAA[C/T]GGTGCTGGAATTGAG	10391
rs369132896	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727138	GTGTGTCTCAGCACC[A/G]CTATCTCAGCCACTT	10391
rs369192239	snp	C/T	0.000115505	0.00759862	intron-variant	CORO2B	GRCh38.p7	15:68719131	GTCCTCTCTTCTGCT[C/T]CTCCCACTGTAGTCA	10391
rs369204264	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68564539	CTGGTCTCAAACTCC[C/T]AGGCTCAAGCGATTG	10391
rs369205167	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68634669	CTCGGGCCCCACCCT[C/T]GACTTCCTGAATCAG	10391
rs369223156	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68714141	GGGCCCGCACACCAG[C/G/T]TTCTCATAGCATTCC	10391
rs369232667	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68650205	GAAACCCCGTCTCTA[C/G]TAAAAATACAAAATT	10391
rs369281821	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68667069	CTCCCCAGGCTCCCC[A/G]CTCCTGATCTCCCTT	10391
rs369286922	in-del	-/C	0.0830808	0.188181	intron-variant	CORO2B	GRCh38.p7	15:68597617	CCCTAATTTCTGTTT[-/C]CCCCCCCATCAAAAA	10391
rs369325240	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68717279	AGATCACACCACTGC[A/T]CTCCAACCTGGGCAA	10391
rs369326788	in-del	-/TCC			intron-variant	CORO2B	GRCh38.p7	15:68656169	CTCCCCCTCGCACCG[-/TCC]CCCCCGCCCCCCGAC	10391
rs369344546	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68720065	CCCAGCGGTATTTCG[C/T]TCCAGCCCACACCCC	10391
rs369359607	snp	C/T	0.000153988	0.00877328	intron-variant	CORO2B	GRCh38.p7	15:68719244	ACCGAGGTACCACAG[C/T]GGGGGGCTCCACAGA	10391
rs369368784	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68582958	CACAATTGCCTGCTG[C/T]ACCTTAGAAGGCCTT	10391
rs369370534	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68650440	ACATGGTGAAACCCC[C/T]GTCTCCACTAAAAAT	10391
rs369373633	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589942	CTACATGCCTGGCTG[C/T]CCCCCTGGCCTCCAC	10391
rs369374980	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68562099	ATGATGTTGTCCTCC[A/G]GCCACCCCTTCCCAT	10391
rs369407391	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68559548	GCGAAGTTGACCGTG[C/G]CAAGCCGGCCCGCTG	10391
rs369462275	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68686194	GGCATGTGCCACCAC[A/G]CCTGGCTAATTTTGT	10391
rs369470457	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668499	TTAGGTAAGACAGTC[C/T]GAAGGACCTCTCTGC	10391
rs369491835	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727388	TTCATTTCCCACTAC[A/G]CACAAAGAGTTTATA	10391
rs369501914	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68706301	ACACCCTCTCTTCCA[A/G]CACTGCTCCTCCCAG	10391
rs369505105	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639653	GTTCCACATCGTCCT[G/T]AATCGGAGGTCATCC	10391
rs369513188	in-del	-/T	0.0146672	0.084371	intron-variant	CORO2B	GRCh38.p7	15:68569053	CCATATGCCCCCTGC[-/T]TCCACACACACACAA	10391
rs369521241	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68558759	ACCTCCTTTCTAGGC[C/T]TTTGTGGAGGCTGCA	10391
rs369529481	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68574388	TCCCTGTGGCCTCTG[A/C]CACAATGCAGCACCC	10391
rs369531548	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68721761	ATTTATTTATTTATG[-/T]TTTAGAGACAGAGTC	10391
rs369546745	in-del	-/TTTA	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68569519	CTGGATGTACCACAG[-/TTTA]TTTATCTGTTCACCT	10391
rs369548167	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68647729	AGAAGGGACTGGGGC[C/T]AGGTGCCGTGGCTCA	10391
rs369549351	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650932	GCCCTCTGGTCAGAT[C/G]AATGTCTTCATCTGC	10391
rs369557060	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569119	ACATTTGTTACAATC[A/G]ATGAATCTACATTAG	10391
rs369615843	in-del	-/CCT			intron-variant	CORO2B	GRCh38.p7	15:68685301	CTTCAACCTCCTCCT[-/CCT]GGGTTCAAGCCATTC	10391
rs369684167	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68714290	TCCAGAGAGATTGAG[A/G]GACTTACCTGGGGAC	10391
rs369691051	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68701439	GCCTCAGCCTCCTGA[C/G]AAGCTGGGACTACAG	10391
rs369691836	in-del	-/CT			intron-variant	CORO2B	GRCh38.p7	15:68719322	TCCTTGTCTGTCCCC[-/CT]GTTTGAACTTCCCTC	10391
rs369693166	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68709626	TACACCCGGCTAATT[G/T]TTGTTTCTTTGGTAG	10391
rs369704417	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68719051	AGGAGAGCAGGTAGA[A/G]TGACTGGAGATCAGT	10391
rs369709587	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68673972	TCGGTGGACCCAGAA[A/G]CAGCAGTAGGAGCTT	10391
rs369750793	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68586244	GCACTTACCATATGC[C/G]TGACATGTAGTGTTA	10391
rs369781686	snp	C/T	0.000199724	0.00999109	intron-variant	CORO2B	GRCh38.p7	15:68714048	TGGGACCAGGTCAGC[C/T]ACGGGGAGGCCTGCT	10391
rs369800970	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68599365	GCGCCACAGATCCCA[C/T]TGGGTGCTCCTGCTG	10391
rs369820830	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68642491	TTTGGCTCCCTGAGC[C/T]TCAGGTTCTGGTGTC	10391
rs369834620	snp	C/T	3.30082e-05	0.00406239	synonymous-codon	CORO2B	GRCh38.p7	15:68711643	GGACGGCAGCCTGCT[C/T]ACCACCACGTGCAAG	10391
rs369836873	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68561556	TCAATCTTGCTGCAG[C/G]GAGGGAGGCAGACAG	10391
rs369857287	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68642933	GAAACTGTGGCATCG[A/G]GAATGTTCTGCATGG	10391
rs369869660	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648269	ACCCGGGAGGCAGAG[A/G]TTGCAGTGGGCGAGA	10391
rs369879199	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68681490	TTTCTGTCAGAGAAG[A/G]AGTCTGGGAAAAGGT	10391
rs369885206	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577786	TCCTGGAGGCTGGTT[A/C]CTCTATTATTATTGC	10391
rs369888035	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68716034	CCCTGTGGGTCTGGT[A/G]TTATGGACAGGGCCT	10391
rs369974588	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68559384	CATCCATTTTAGAAG[A/T]TCTGGTCAATCGTTC	10391
rs370058363	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68723200	AATCTTGACTCACTG[A/C]AACCTCCACCTCCCG	10391
rs370083446	snp	A/G	1.71702e-05	0.00292998	missense	CORO2B	GRCh38.p7	15:68645170	CACAGATGTCCTGGC[A/G]TCCGCAATACCGTAG	10391
rs370087973	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68562890	GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCGGGA	10391
rs370108197	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68625952	GTTGTGGGTATCAGT[A/C]GTTTGCTCCTTTTAT	10391
rs370121572	in-del	-/AAA/AAAA/AAAAA			intron-variant	CORO2B	GRCh38.p7	15:68691624	GCGAGACTCCGTCTC[-/AAA/AAAA/AAAAA]AAAAAAAAAAAAAAA	10391
rs370172565	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68575341	GAGAATACACCTTTT[C/T]CTTTTTTTTTTTTTT	10391
rs370206433	in-del	-/CT	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68580828	AACTCAGCGCCTCCC[-/CT]GTGTCTCTTTTTGTG	10391
rs370237698	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68657353	AAGACACCATCTCTA[C/T]GAAATACAAAAAAAT	10391
rs370281045	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68566982	TGGCTGATCCCCACT[C/G]TCCCACTTGGGTCTG	10391
rs370333591	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68645899	CTGCCTCAGCCTCCC[A/G]AGAAGCTGGGATTGC	10391
rs370336498	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68657634	TGTAGGACACAGTAA[C/T]GACTCTAATTTCAAA	10391
rs370341225	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68591001	CTGAGCCCTGTGTGC[C/T]AGGCCCTAAGCGGCA	10391
rs370348721	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68632643	TCATCCAGGCTGGAG[G/T]GCAGTGGTGCTATCT	10391
rs370355639	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68617179	GGCTCCAGGGAATGG[A/G]ATGAGTCATATCCTG	10391
rs370369523	snp	A/G	0.000153988	0.00877328	synonymous-codon	CORO2B	GRCh38.p7	15:68695253	GTGCTCGGAGGACAC[A/G]TCGGTGAGCAGAGGG	10391
rs370408788	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68686104	GTGCAATGGCGCAAC[A/C]TTGGCTCATTGCAAC	10391
rs370418393	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566610	CTGTTGCCTGTCCCC[A/G]CACCCCTCACTCTGC	10391
rs370419859	in-del	-/CCCC			intron-variant	CORO2B	GRCh38.p7	15:68575577	TGACCTTGTGATCTG[-/CCCC]CCCCCGCCTCGGCCT	10391
rs370453502	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68660278	TATGTCTTCTTCCTC[A/G]TTGTCTGGCATTGCT	10391
rs370492322	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698462	GTGCCTCATGCTCCA[A/G]GACCCCAGCTTGTAA	10391
rs370497954	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68651231	AGCCAGCGCCGGCTT[C/T]CCCTGCCGCCCAAGC	10391
rs370518347	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591684	CTCTCCCTGTGCCTG[A/G]GAGCTGGGTGTCACA	10391
rs370575099	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68672046	TGATGGGGCCCACAG[C/G]AATAGTGAACCGGGG	10391
rs370587519	in-del	-/CA	0.175576	0.238665	intron-variant	CORO2B	GRCh38.p7	15:68602408	AAATTAGGGGCTGAT[-/CA]CACACACACACACAC	10391
rs370603223	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652711	TCTGTTTGAATCTCA[C/T]CTCAAGTTCTATGAT	10391
rs370673977	snp	A/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68707278	TTTTTAAAGGTATAG[A/T]TTTAGAGGCATAATG	10391
rs370699684	snp	C/T	4.96627e-05	0.00498286	intron-variant	CORO2B	GRCh38.p7	15:68719252	ACCACAGCGGGGGGC[C/T]CCACAGAGCACAGGC	10391
rs370793477	in-del	-/CGTG			intron-variant	CORO2B	GRCh38.p7	15:68709456	AAAAGATTTTTTTTT[-/CGTG]TTTTTTTTTTTTTTT	10391
rs370806625	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68583141	AGGGCACAGCCTGCT[G/T]ATAAGAGCCAGTGGC	10391
rs370811211	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68562980	AGACTCCATCTCAAA[A/G]AAAAAAAAAAAAGAA	10391
rs370825894	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605977	GATTCGCCCACCTTG[A/G]CCTCCCAAAGTGCTG	10391
rs370827957	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68655389	GTCCATGCCTCTCGC[C/T]GGCCCTCCTCCCCAG	10391
rs370828447	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68691877	ACCTATTGACTGGTT[C/T]GGTGCCTTTCAGATT	10391
rs370828780	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68563736	CAGAAAGAAAAAAGA[C/T]TATAAATGAATAAGA	10391
rs370871931	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671569	GGTCTCATTTGGTTG[C/T]GTTAAAGCTGTCGGC	10391
rs370879460	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68706788	GATCATAGCTCACTG[C/T]AGCCTCGTCTTCCTG	10391
rs370884029	snp	C/T	0.000123225	0.00784839	intron-variant	CORO2B	GRCh38.p7	15:68710693	CAAGGGACTTCTTGG[C/T]CGTGTCCACCCAGCC	10391
rs370887038	snp	A/C/T	0.000138239	0.00831285	missense, synonymous-codon	CORO2B	GRCh38.p7	15:68710800	GCTCCTGGAGCTGCA[A/C/T]GGGCACAGCCGGCGT	10391
rs370903795	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640924	GTCTGAATGGGGAGC[A/G]GAGCCAGGACTGCAG	10391
rs370903805	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588145	AATCTGTGCCCACTC[A/C]TTTCCTCTTCCTCAC	10391
rs370908083	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68575356	TCTTTTTTTTTTTTT[C/T]CCTCTGAGACTTCGT	10391
rs370925588	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68608135	GCTACCTACCTCTGG[A/G]GCAAGGTTTCCTTCC	10391
rs370929879	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68576691	TGGCTAGAGGCTGAC[C/G]TGCCCAAGACAGCTG	10391
rs370935624	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68627343	ATGCACCAGGGCAGG[A/G]CAACTTGCCCTCAGT	10391
rs370940552	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68620520	TGAGTCTGATAAGTT[A/G]TTTTAAGCCACAGGA	10391
rs370940853	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68642035	AACCCGGCCTAGCCT[C/T]TTTTTTTTTTTTTTT	10391
rs370947270	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68586925	AAGGAAACTTTGCTC[C/T]GGCAGGAAATTTTCC	10391
rs370951930	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68661081	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAA	10391
rs370966777	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68707064	CTCCCAGGTTCCAGC[A/G]ATAGTCCTGCCTCAG	10391
rs370969909	in-del	-/GA			intron-variant	CORO2B	GRCh38.p7	15:68573311	CAAAGAGAAGAGAGA[-/GA]CGTCCACAGAGACAG	10391
rs370996636	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68597137	CAAATTGCGTAAAAC[C/G]AAAGAGCAATTAAGA	10391
rs370999693	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68610540	TCCTCTCTCCCCTCC[C/T]GTTCTCCCATCCTTC	10391
rs371044107	snp	A/G	0.000153988	0.00877328	intron-variant	CORO2B	GRCh38.p7	15:68710910	AGGCAGCTGGGTGGA[A/G]AGGGATTGGGGAAGA	10391
rs371081336	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637897	AATTTTGCTCATGTC[A/G]TCATCTAGAAAATGC	10391
rs371089295	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68653517	AGCCCATCCCCACCA[A/G]ATCCTAGGGAGAATG	10391
rs371103578	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68592721	AGATGGAGAGGCTGG[G/T]CTGTGTACTGTACAG	10391
rs371110072	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68580663	GGGGTAAGATGCTTA[C/G]GGTTTTGAAATGATG	10391
rs371138812	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68646277	GCCCGTGGGAGGTCA[C/T]GCGCTTCAGGGAAAG	10391
rs371145814	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68674724	CCATGACCTCACCAG[A/G]CAGGGTTGGAGTAAG	10391
rs371150276	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68560371	GCAATCATGGCTCAC[C/T]GCAGCCTCAAACTCC	10391
rs371156753	snp	A/T	1.66261e-05	0.00288319	intron-variant	CORO2B	GRCh38.p7	15:68715343	CTGCCACAGCTGGTG[A/T]GCTCATGGCACGGGA	10391
rs371161531	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68725458	TGTATTATTATACAT[A/C]TATTATTATGTATTA	10391
rs371181401	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703262	TTCAAATGATTCTCC[C/T]GCCTCAGCTTCCCGA	10391
rs371215024	snp	C/G/T	1.67778e-05	0.00289631	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68725988	AGCTCCCCAGCTGGG[C/G/T]TGTTTTCTAAGCCGA	10391
rs371239183	snp	C/T	8.52798e-05	0.00652937	missense	CORO2B	GRCh38.p7	15:68645173	AGATGTCCTGGCGTC[C/T]GCAATACCGTAGCTC	10391
rs371295018	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68693917	CTTGGCTCACCGCAA[C/T]CTCCGCCTCCTGGGT	10391
rs371298561	snp	A/G	3.32751e-05	0.00407878	synonymous-codon	CORO2B	GRCh38.p7	15:68718783	CAAGGGCCTGATCGA[A/G]CCCATCTCCATGATC	10391
rs371313642	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68718950	AATTTGGGGTGAGGG[A/G]CATTCTCAGATGGGG	10391
rs371342226	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615492	GCTTAGGCTTAGATG[A/G]GAAGCAGAAGTGCTA	10391
rs371349345	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68644421	ACCCCAGATGACTTT[A/G]ATACAGGTGATCTGT	10391
rs371352215	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68691611	GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA	10391
rs371355619	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68648020	GCAACGGAGAAAGAT[C/G]CTGTCTCTCAAAAAA	10391
rs371357749	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606583	CAAATTCTGGCACAT[A/G]GCCTGAGAGAATTTT	10391
rs371358388	snp	C/T	4.95716e-05	0.00497829	synonymous-codon	CORO2B	GRCh38.p7	15:68711592	GAAGATGATTGACTG[C/T]CACACGGATGTGATC	10391
rs371381473	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68621405	GACCAGAGAGGCTTC[A/G]CAGCGCTGGAGACAT	10391
rs371396201	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577338	CTTGGGCAATTCCCT[C/T]CCCTTCTCTAAATCC	10391
rs371409316	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68715504	GGCGCTGTCACCCCA[C/T]TGTGCTCACATCCAC	10391
rs371414580	in-del	-/T	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68561158	GGAGCTTGAAGAGGG[-/T]TTTTTTCCAGAATCT	10391
rs371436772	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623301	TCTTGAATCAAGTCA[C/T]TGAGACTCGCCAGAG	10391
rs371444851	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68641524	GGACGAGGAAGAGGT[A/G]AAGTCAGATGGGAAA	10391
rs371447438	in-del	-/A/AA/CA/T	0.498927	0.0231381	intron-variant	CORO2B	GRCh38.p7	15:68705436	GGTGAAACTCTATCT[-/A/AA/CA/T]AAAAAAAAAAAAAAA	10391
rs371473857	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616498	GCTGGCTTTACTGCC[A/G]TGCTCCACTCCCTTA	10391
rs371494805	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68574293	GCATGTGGGCATGCC[A/G]CCTGGGGTGGCATAA	10391
rs371503400	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68634322	CTCTTTTACTCACTC[A/G]CTGGCCGGCAGGGTG	10391
rs371564290	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68639200	TGCTTGACCTTGGCT[C/T]TTGCCCCCCTACCAT	10391
rs371566259	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68619886	CGTCACTCTCATTTT[A/G]TAGAAGATGAAAGTG	10391
rs371570835	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68715149	CTTCAGCTGGCTCCT[A/G]GGACCAGGCCCTGCT	10391
rs371615862	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68704743	CTGGGTATGTTCTGT[A/T]GGGTTGAACATCACT	10391
rs371681508	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668067	GCCTGGTGCCACTGA[A/G]TACTCAGCAACCTTG	10391
rs371684047	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68583959	GGCCTTCTTCCAGAT[A/G]TCCAGCATTCTCATG	10391
rs371700797	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642336	ACCCTTCCCCTTGTA[C/T]CCCAGGGAGAGCCTG	10391
rs371735553	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68593068	CATAGTGAGTGTGTG[A/G]GACAGAGAGAGGAAA	10391
rs371738574	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68705181	ATTAACTAATACTAT[C/G]TAAATGTGCAGATGA	10391
rs371774341	in-del	-/GACT			intron-variant	CORO2B	GRCh38.p7	15:68681729	AGAGAAAGGGGAGCT[-/GACT]AAGTCAGGATTCCTG	10391
rs371777051	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68612051	CAGAGGCTATAGGCA[-/G]GGAGCCACTGCACCC	10391
rs371790753	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68680988	GGAGGCTGAGGTAGG[C/T]AGATCGCCTGAGGTC	10391
rs371800269	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68711910	GGGAGGGACCTCATA[A/C]CCTTTCCTGTCCCCA	10391
rs371861715	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702815	TATCTTTTTCTTTTT[C/T]TTTTTCTTTTTTTTT	10391
rs371896530	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68650229	CAAAATTAGCGGGGC[A/G]TGATGGCAGGTGCCT	10391
rs371924948	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68676974	GAGACAGGTTTCACT[A/G]TGCTGCCCAGGCTGG	10391
rs371930346	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703755	CAGTCATGACCCTCA[A/G]CATGTCAGAAAGCAG	10391
rs371931175	snp	A/G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68651892	TTCCATATTTATGAT[A/G/T]AAAAATTCTTCTGCA	10391
rs371942469	snp	C/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615325	TCAGTCATTTTCCCT[C/G]GACCAGGACTCTTGA	10391
rs371977004	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564434	TCAGCCTCTCGAGTA[A/G]CTGGGACTACAGGAG	10391
rs371995483	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68584621	TGGCACCCGGGCAGC[C/T]CTGACTCTGATTTGG	10391
rs371998970	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654786	GTTACCCATCTCCAG[A/G]CCACCCCATCCTAGC	10391
rs372018623	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68716311	AAGTCTCAGTTTCCT[C/T]ATCTGTAAAATGTGG	10391
rs372054157	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68594718	GCAGAGGTGGAATTT[C/T]TTTGGGTTTGAAGTG	10391
rs372110557	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68627052	TTAGCAAGGTACTTA[-/A]CCTTTTTTCTGCCTC	10391
rs372112379	snp	A/C/T			intron-variant	CORO2B	GRCh38.p7	15:68584996	GGGAGAAGCCACCAC[A/C/T]GCCCTTCCTCATCCC	10391
rs372156134	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600262	AAATTGCACTCCTCC[A/G]TGGAGGCCTGGCTCC	10391
rs372164240	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725754	TGTGAGGGCACGGGC[A/G]GCAGGCAGCTGGAGA	10391
rs372164333	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68642786	AGGTCACTGTGGACT[A/G]TGTAGATCAGAGTGA	10391
rs372165483	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68724077	CGTGATGGCACACAC[C/T]TGTAATCCCAGCTAC	10391
rs372169271	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68598411	TCTCTATTTTGCGTG[A/G]TCAGTGATTTTTACT	10391
rs372199494	snp	A/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68708165	TTGCCTTTCTTACCT[A/T]GAAACCTCCCAGTCA	10391
rs372207932	snp	C/G/T	0.000250025	0.0111782	intron-variant	CORO2B	GRCh38.p7	15:68719380	GACAGTCCATGGGAT[C/G/T]GTCAGTGAGAGCGTT	10391
rs372242875	in-del	-/GT			intron-variant	CORO2B	GRCh38.p7	15:68608532	AGTGTGCACGCGTGC[-/GT]GTGTGTGTGTTGGGG	10391
rs372267861	snp	A/G	0.000153988	0.00877328	missense	CORO2B	GRCh38.p7	15:68719443	CTTTGAAAGAAGGCT[A/G]TAAGAAGTCCTCAAA	10391
rs372268624	in-del	-/AAG	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68569015	AAAGCACATAAAAAA[-/AAG]AAGAAAAATACACTA	10391
rs372309594	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68708544	TTTTTGTATTTTTTT[-/T]AGTAGAGATGGGTTT	10391
rs372320304	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68664355	TAACCTCTTAAAAAC[A/T]GAGAGTTATTGGCGG	10391
rs372335498	in-del	-/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68709889	ATAAGGTAGGTGGTA[-/G]GGTGGGGGGAACATC	10391
rs372403740	in-del	-/AAAACCCCCC			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727179	CACGTAGAATGACCA[-/AAAACCCCCC]CAGCCACTCGCATCC	10391
rs372420971	snp	A/G	1.8563e-05	0.0030465	intron-variant	CORO2B	GRCh38.p7	15:68718842	TGGGCTCCAGGAGGG[A/G]GGCCTGCATCGCCTC	10391
rs372424321	snp	C/T	1.64825e-05	0.00287071	synonymous-codon	CORO2B	GRCh38.p7	15:68714582	CTCCATGCCCCTGAT[C/T]GAAGAGGAAATTGAT	10391
rs372427198	snp	C/T	1.68502e-05	0.00290255	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726004	TGTTTTCTAAGCCGA[C/T]CTCTCCGTCGTTTCT	10391
rs372439439	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68705752	AGGCTCCTAGGCAGA[A/G]CTGTCACCTCAGCAT	10391
rs372448476	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68693561	GAAAAAGACCTGAGA[A/G]ATGGAAGCATAGCTT	10391
rs372464048	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68621650	TTTGGTTTGGTTGTT[G/T]GTTTGTGTTAGGGAA	10391
rs372476075	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68600299	ACCTCCTCCAGGAAG[C/G]CTTCCTCAATGTTTG	10391
rs372496796	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68713897	ATGTTGGGGACCCTG[A/G]CTCACCACCTCCCTC	10391
rs372504835	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68667210	CTCACCTGCCCTCAC[C/G]AGACCTTGAGCCAGC	10391
rs372529370	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68676321	GGAGTCATGATGAGC[C/T]GCACAAACCCTCCAG	10391
rs372561546	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68563632	TCAACAAAAGTGACA[C/T]ACCTTTAGCTAGACT	10391
rs372570369	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68649467	GGGGTAAACAAATTA[A/G]GGAAGAGCCACACAA	10391
rs372584293	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68681855	CAGATGTAGTTATCT[C/G]TTGCTAGCAACAGAA	10391
rs372587200	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574450	GCTGCAGGTAATCCT[A/G]AAAGACTGCAAGCCC	10391
rs372605598	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68561777	CATGTGCCTGTGTGA[A/G]CGGAGCATGTTTCCG	10391
rs372623777	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68567260	AAAAGCACATAAATT[A/G]TATTAGTTTTACATG	10391
rs372628504	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625196	GTTTAGGAATCTCTA[A/G]ACTTGAAGCTTTTCC	10391
rs372646493	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68581610	TGGTTCCAATGATCT[C/T]TAGGGCCTCTTCTGC	10391
rs372675780	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591130	CAGGGATGTTGGGGA[A/G]GGGAGGCTGATGGGT	10391
rs372682298	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68636721	TAAGTCCCTGTACAC[C/G]CCACCCAGGAACTTC	10391
rs372729171	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564541	GGTCTCAAACTCCTA[A/G]GCTCAAGCGATTGGC	10391
rs372798738	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68646603	GCATGCACTTGATGG[C/T]GGGAGGTCTGGGTTC	10391
rs372805181	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68662134	GGTTGGCAGAAGCTG[C/G]TTTTCCTGTTATCAC	10391
rs372810353	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68696487	CTGGAAGGCGGAGGT[C/T]GCAGTGAGCTGAGAT	10391
rs372813410	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68585582	ACTCCAGAGAACACT[G/T]TCATCTCACTTCCAG	10391
rs372829532	snp	A/C			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630526	TGCTGTGGGGGCAGA[A/C]AGACCTCATGGGGAC	10391
rs372831047	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68722640	TGAGAACTTGGAAGA[C/T]GCAAGAGTGTGTAGA	10391
rs372835828	snp	C/T	0.000940788	0.0216682	intron-variant	CORO2B	GRCh38.p7	15:68719103	TAGGGGCTTTCCCAG[C/T]AGCCCCCCATGTGTC	10391
rs372839722	snp	C/G	3.31109e-05	0.00406871	intron-variant	CORO2B	GRCh38.p7	15:68719246	CGAGGTACCACAGCG[C/G]GGGGCTCCACAGAGC	10391
rs372843642	snp	C/T	3.31972e-05	0.004074	synonymous-codon	CORO2B	GRCh38.p7	15:68645195	CCGTAGCTCCAAGTT[C/T]CGGAATGTCTACGGG	10391
rs372852683	snp	A/G	6.63757e-05	0.00576051	intron-variant	CORO2B	GRCh38.p7	15:68714508	CTGGGATTTGGGGAG[A/G]GGTATGCCATCCTGC	10391
rs372854914	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68669243	CCTTGAGAAGCAGGG[A/G]GCCCTGTTCACGCCC	10391
rs372881912	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68611770	TCCAATTTTCCACTT[C/T]TTTTCTTTTTTTTTT	10391
rs372903006	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68582967	CTGCTGCACCTTAGA[A/G]GGCCTTAGGAGAGGG	10391
rs372906356	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68590242	CCCCTCTGCACCACC[A/G]CCCCCCTCTCCCAGG	10391
rs372941637	snp	C/G	0.000416108	0.0144181	intron-variant	CORO2B	GRCh38.p7	15:68725812	GCTCTCTCCTGGGCC[C/G]TCCTTGGCCCCCTCT	10391
rs372971542	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68576177	AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA	10391
rs372988980	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652220	TCTTATTCGGGCTGC[C/T]GTTGTGAAGGCCAGT	10391
rs372990931	snp	A/G	0.000199366	0.00998215	intron-variant	CORO2B	GRCh38.p7	15:68718853	AGGGGGGCCTGCATC[A/G]CCTCTTAGCCTGCTC	10391
rs373005259	snp	C/T	0.000199074	0.00997484	intron-variant	CORO2B	GRCh38.p7	15:68695276	GCAGAGGGGTGCTCC[C/T]GGAGGAGGGTGGGCT	10391
rs373009911	snp	A/C	1.66302e-05	0.00288355	intron-variant	CORO2B	GRCh38.p7	15:68725828	TCCTTGGCCCCCTCT[A/C]TTCCTCCACCCCAGC	10391
rs373012033	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68723948	GGTGGCTCACACCTG[A/C]AATCCCAGCACCTTG	10391
rs373133568	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68673995	AGGAGCTTATGGCAA[A/T]AGTTAGAAGGAGGCG	10391
rs373143907	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68612737	AACTCATGATCCTCA[C/T]GCCGCAGTCTCCTCC	10391
rs373177433	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68570569	TGTGCCCACAAAGTG[A/C]GCTGATCAGAGGAAC	10391
rs373180075	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68721113	TCTTGAACTCCTGAC[C/T]TTAGGTGATCCACCT	10391
rs373220035	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631948	GGCCACATGCCATCC[C/T]TCAGCATCGCTGGAG	10391
rs373231009	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68565655	TCATTGTATAGTGGA[C/T]GGGATGACCCTCACT	10391
rs373253280	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68559028	TTTAGTCAGTAAATA[C/T]GTTCGGAGATCCTAC	10391
rs373283613	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68710651	ATCTCAGAAAGCCTG[C/G]TGTCCGAGGAAAGGG	10391
rs373294905	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68590908	CTGCCCTGTTCTCCT[A/G]TGCAGGGCCGGCCGC	10391
rs373297198	snp	A/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605770	CTGTGTCGCCCAGGC[A/G/T]GGAGTGCAGTGGCGC	10391
rs373298971	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68687579	CATGCCACACACACA[C/T]ACTGAAATGCACTTT	10391
rs373299546	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68569964	TGTGATCTTTGGCTG[A/T]GGAGTCATTGGTCAG	10391
rs373323634	snp	A/C	0.0119091	0.0762411	intron-variant	CORO2B	GRCh38.p7	15:68656075	TGCCTGAGAAACTTC[A/C]GGCCTGATTTAGTCC	10391
rs373331789	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68655174	AAGGTTTTACCACAG[A/T]GCCTGGCGTACAGCA	10391
rs373340146	in-del	AAA/T			intron-variant	CORO2B	GRCh38.p7	15:68597635	CCCCCATCAAAAAAA[AAA/T]AAATAAATAAATAAA	10391
rs373351639	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68626619	AAGCAAGAGACTCAG[-/AG]TCTTCCCGGGAATCA	10391
rs373354451	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626192	TGAGGGCACACAGTT[C/G]CAGTGCTTACAGGGC	10391
rs373363761	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68720250	CAAGTCTACTGACCT[A/T]TATAAGTCCATTTCC	10391
rs373365424	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68643535	GAAGTAGGGAGGAGC[A/G]GAGAGCAGGGAGACT	10391
rs373402331	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68644686	GGTTGCCTTCTTGCA[C/T]GTGGAGAGACATCTC	10391
rs373405612	in-del	-/AA	0.0103295	0.0711199	intron-variant	CORO2B	GRCh38.p7	15:68565522	AACATTTTTTCAAAT[-/AA]AAAAATAAATATATA	10391
rs373412432	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68717273	GAGCTAAGATCACAC[C/G]ACTGCACTCCAACCT	10391
rs373427035	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682169	CTCCAAATCAGGAAG[A/G]GGGCTTGGATGCCCA	10391
rs373434126	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68666787	TCCTTTCTTATCTAC[A/G]CTATTGCAATCACTG	10391
rs373434764	snp	A/G			downstream-variant-500B	CORO2B	GRCh38.p7	15:68727921	GGAATGACAACCCAC[A/G]TCTGTACCTACAGAT	10391
rs373440240	snp	A/G	1.64868e-05	0.00287109	intron-variant	CORO2B	GRCh38.p7	15:68715167	ACCAGGCCCTGCTCT[A/G]CCCTCCCTACCTGCC	10391
rs373458695	snp	A/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68608384	CCCCACACTGTGGTC[A/C]CCTGGAGGACTTCGG	10391
rs373465371	snp	C/T			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632201	GCATAACTCCTTGGG[C/T]GCTATTCATCCACAC	10391
rs373470521	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68618824	CCTAGACATGTGCCC[C/T]TAAAAATACTTTGAG	10391
rs373479309	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566015	CCACCTCTGTGGAGA[A/G]GCAGCTGACAAATGC	10391
rs373495885	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68714504	CTTCCTGGGATTTGG[A/G]GAGGGGTATGCCATC	10391
rs373505897	in-del	-/CCAAAAA			intron-variant	CORO2B	GRCh38.p7	15:68664663	AAAAAAAACCAAAAA[-/CCAAAAA]ACAAAAAAACCTGAG	10391
rs373561139	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68715182	GCCCTCCCTACCTGC[C/T]ACCTTCCTCAACTCC	10391
rs373627365	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68661262	GGATTATAGGCGTGA[A/G]CCACCGCATCTGGTC	10391
rs373642309	in-del	-/AA/AAA			intron-variant	CORO2B	GRCh38.p7	15:68657517	ATGAGATCCTGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA	10391
rs373667309	in-del	-/TT			intron-variant	CORO2B	GRCh38.p7	15:68722083	AAAGAACTCTACTCT[-/TT]GAAGATAGAGACACA	10391
rs373730983	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699626	AGTACAGCCCTGAAC[C/T]GCATCTTACCCGGGT	10391
rs373739350	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68698591	AGACCACGGTATGCC[G/T]TGCACCACCCTGGCT	10391
rs373748977	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68619692	GTGTATATATATATG[C/T]ACACATACATATGTG	10391
rs373767771	snp	A/G/T			intron-variant	CORO2B	GRCh38.p7	15:68680392	GGGCAACAAACACCC[A/G/T]TGAAATAAAGCAAAC	10391
rs373773728	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68666291	ATGCAAATACTGAAA[A/G]TGAGGCCCCAGGCAG	10391
rs373779513	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68724395	ATAATTTAAAGTTCA[A/T]CTGAAAGCAAAGTCC	10391
rs373803494	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68562921	GGTGGAGCTTGCAGT[C/G]AGCCGAGATCATGCC	10391
rs373832885	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68605157	AAAAGAAAAACTTCA[A/G]TCTCCCAGCTGCTTA	10391
rs373933999	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68671108	CACTGAGGAATACAA[C/T]GCAGCCGTGAAAATC	10391
rs373947201	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678439	AACACTTTGGGAGGC[C/T]GACTTGGGCAGATCA	10391
rs373950332	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68714223	CTTCAAGGAACAATG[A/T]CGGCCACACCTGCAA	10391
rs373957064	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68608902	CATCCATCCGTTCAA[C/G]AAGTGCTTACCAAAA	10391
rs373958764	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595650	AAGTTAATAACAGTT[A/G]TTATCACTAGACCAA	10391
rs373963241	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68623348	TTGACTGAAGCTGCT[A/G]GATGCAGACCCTGGG	10391
rs373966146	in-del	-/ATACACACACACAC			intron-variant	CORO2B	GRCh38.p7	15:68587048	TATAGGGAGATATGT[-/ATACACACACACAC]ACACACACACACACA	10391
rs373966319	snp	C/G	0.000153988	0.00877328	missense	CORO2B	GRCh38.p7	15:68710819	CACAGCCGGCGTGTG[C/G]GGCTGGTCGAGTGGC	10391
rs373974126	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727276	CCTTCTGCAGATGAG[A/G]AAACCGAGAGAAGTG	10391
rs373983731	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566664	CCCTGTGGTTAAGGA[A/G]CAAATAAGGCTCCAT	10391
rs373991459	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68722959	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	10391
rs373992076	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68652818	GCACGGCCCACAAGT[A/G]GCAGAGTCAGAATTT	10391
rs374000415	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68629202	GTAGTTCTGAATGAG[A/T]CAATGTCTGAGAAAA	10391
rs374002203	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68723091	AAAAACAAAAGGAGA[G/T]AATCATAAAAATGAT	10391
rs374023266	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68669685	CAATGGTGGGTTTTG[A/G]GCTCAACAAAGAAAC	10391
rs374029285	snp	A/C	3.39605e-05	0.00412057	intron-variant	CORO2B	GRCh38.p7	15:68645379	GGTGGCCCCTACCTT[A/C]ACTCCAGCTGCAGCT	10391
rs374079556	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694754	TGAACAAGGCAGATC[A/G]TGGGCCTGTGTGTGT	10391
rs374080561	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68626834	AGGAGGTCTGGTCAG[A/G]GGCTGGGGCCCCAGC	10391
rs374103225	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68706575	TGCTTATGCACCAAG[A/G]TACAGTATGAGACAT	10391
rs374112454	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68683870	GAGGTGGAGGTGTAT[A/G]ACCATGGGCATGGCA	10391
rs374119827	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68707329	GGTTAAAAACTAGGA[C/T]AGTTTTTGGGGACAA	10391
rs374120237	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68685207	TATTAAATGTGCATG[A/G]TAATGTTCTTAATTT	10391
rs374122575	in-del	-/ATT			intron-variant	CORO2B	GRCh38.p7	15:68603353	TGTAACCTCCAAATA[-/ATT]ATTATCTTAAAAAAA	10391
rs374133713	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68701546	GCTGGAGTGCAGTGG[C/G]GCGATCTCGACTCAC	10391
rs374167960	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68713603	CTTCTGGGGGTTGCC[A/G]GCTCCCGTGGCTGGT	10391
rs374173966	snp	A/G	1.64923e-05	0.00287156	missense	CORO2B	GRCh38.p7	15:68715285	ACCTCATGGAGTTCC[A/G]CTCCCCAGCCCCGCA	10391
rs374202453	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633467	CCTCAGCTGGTGAGG[C/T]CCCTTGAATTGTTTC	10391
rs374209390	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68571872	GGTATTTAGCCCCAA[A/G]GAGGTGGTAAGGGCT	10391
rs374256356	in-del	-/CGTGAGTGTGTGT			intron-variant	CORO2B	GRCh38.p7	15:68561906	GCCTGTGAGCATGAC[-/CGTGAGTGTGTGT]TGTGAGTGTGTACAC	10391
rs374285924	in-del	-/GGAT			intron-variant	CORO2B	GRCh38.p7	15:68697208	GATGGATGGATGGAT[-/GGAT]TGTTGGATGGATGGA	10391
rs374300405	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68561372	CCAGATGGTCACCCA[C/T]CCCTCCCTCCCCGAC	10391
rs374318945	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68701735	GTGATCTGCCCGCCT[C/T]GGCCTCCCGAAGTGC	10391
rs374332386	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68641617	TTTGCCGGGTGGGCT[C/T]AGGAGAGCCTATCAG	10391
rs374359312	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68596716	CACAGGGAAGATGCA[C/T]CTTCAGGCCTTGGGG	10391
rs374363053	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68648029	AAAGATCCTGTCTCT[A/C]AAAAAAAAAAAAAAA	10391
rs374367235	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68573193	CAGGGCAGGGCCCCC[-/C]AACCCCCAGCATCCC	10391
rs374400326	snp	A/C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726010	CTAAGCCGATCTCTC[A/C/T]GTCGTTTCTACTCAT	10391
rs374424833	snp	A/T	3.29538e-05	0.00405904	missense	CORO2B	GRCh38.p7	15:68714602	AGGAAATTGATGGGC[A/T]CTCTGGCCTCCTGTT	10391
rs374457933	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68558843	ACTGGCTGGGTAACA[C/T]TGGCCAAGTTACTTC	10391
rs374490845	snp	G/T	3.89302e-05	0.00441176	intron-variant	CORO2B	GRCh38.p7	15:68718651	GGGTGATGTCACTGA[G/T]ACGCAGTTTCTGGGA	10391
rs374516427	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68693825	TCAGATCTGGTTGTG[A/T]TTTGTTTGTTTGTTT	10391
rs374520985	snp	A/C/G	8.35465e-05	0.00646277	intron-variant	CORO2B	GRCh38.p7	15:68710712	GTCCACCCAGCCTGG[A/C/G]CCCTCATCTCCCTCT	10391
rs374524832	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68583622	GGATGTGGGGCAGGG[A/G]AGCAAAGTCCATAGG	10391
rs374555474	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68572169	GAGCAGCTCTTCCAG[C/G]AGGCAATCAGGGACT	10391
rs374569592	snp	A/G	6.62669e-05	0.00575578	intron-variant	CORO2B	GRCh38.p7	15:68719266	CTCCACAGAGCACAG[A/G]CGGCTGCAGCCTTTG	10391
rs374589693	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603800	GCCTCCAGAACTGTA[C/T]GAAATAAATATCTGT	10391
rs374601973	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68680518	ACAGTTGCATGGACT[A/G]TACACTGCACAACTC	10391
rs374617311	snp	C/T	0.00279162	0.0372561	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632213	CACAGATGGGCCGTG[C/T]GGATGAATAGCGCCC	10391
rs374672453	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68670058	CAAGACTCTGTCTCA[A/G]AAAAAAAAAAGGGGG	10391
rs374705105	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68707483	AAGTGAACAGAACTT[A/C]GATGTCAATTAATAG	10391
rs374722524	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68604793	GCATTTTTTACTTTA[A/T]TAATTAGGAGAAAAT	10391
rs374753697	snp	A/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68605109	ACAGAGCGAGACTCC[A/G]TCTCAAGGAAAAAAA	10391
rs374763744	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68671271	TTGTTGTTTTTTTTT[-/T]CCTACTTTCTTAAAA	10391
rs374817342	in-del	-/GGGCT			intron-variant	CORO2B	GRCh38.p7	15:68670408	ATCTCTTGAAATCCT[-/GGGCT]CAAGTGATCCTCCTG	10391
rs374828513	snp	C/T	0.000148545	0.00861688	synonymous-codon	CORO2B	GRCh38.p7	15:68711631	GTCCTTCAACACGGA[C/T]GGCAGCCTGCTCACC	10391
rs374859897	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68686333	GAGCCACCACGCCCG[C/G]CTTCATACACTGATT	10391
rs374867483	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595641	TGAGTGGTAAAGTTA[A/G]TAACAGTTATTATCA	10391
rs374881153	snp	C/T	1.68055e-05	0.0028987	intron-variant	CORO2B	GRCh38.p7	15:68711753	GAAGGTATTGAGGGC[C/T]GGGGCTCAGCTTTCA	10391
rs374909186	snp	C/T	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68696306	GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCAG	10391
rs374953789	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68558454	CTCACTGCAGCCTCA[A/G]TGACCTCCCATGATT	10391
rs374961909	snp	A/G/T	0.000204187	0.0101022	synonymous-codon	CORO2B	GRCh38.p7	15:68645174	GATGTCCTGGCGTCC[A/G/T]CAATACCGTAGCTCC	10391
rs374973580	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68677033	CCCATTTCAGCCTCC[A/C]AAAATGCTGGGATTA	10391
rs374994406	in-del	-/TG			intron-variant	CORO2B	GRCh38.p7	15:68629841	GTGTGTGTGTGTGTC[-/TG]TGTGTGTGTGTTGTG	10391
rs375041172	snp	A/G			utr-variant-5-prime, intron-variant	CORO2B	GRCh38.p7	15:68616591	CAAGTCTTCCAGGCC[A/G]CGGTCGAATGATTCT	10391
rs375065342	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68678829	CCAGCCTTCATTGCC[A/G]GTCCTCCAGTGCTCA	10391
rs375065383	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68685035	TGGCCCATGAAAAAA[-/A]CATCTTTCATACTGA	10391
rs375072199	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68723996	CACTTGAGGCCAGGA[G/T]TTCAAGACCAGCCTG	10391
rs375079270	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68702821	TTTCTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT	10391
rs375088257	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68568854	GAAGGAGAGCATCAG[A/G]AAGACTAGCTAATGC	10391
rs375099343	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68590266	TCCCAGGACCAGAGT[A/G]TAGGAGCAGCCTGGG	10391
rs375206896	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68654876	TTTGGCCTTCCTGCT[A/T]CTGTTGTCTGGCACA	10391
rs375217224	snp	A/C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568295	CCACAACAATGCTTC[A/C/G]TTTTCTCATCTGTAA	10391
rs375219618	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610775	AGGTTTGGGAGGCCA[A/G]TAGGGCATCAGGCCA	10391
rs375287600	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577104	TTTGCACAGAGGAGA[C/T]GCCTGAGGTCTGCAG	10391
rs375301792	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68613796	ACTGTGTATACCTGT[A/G]TAGATGGCTGAAACT	10391
rs375371882	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631631	CAGCTTACAGCCTCC[A/G]GGAGAAGTTAATCTC	10391
rs375402506	snp	A/C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633295	TTTCCTTGCTGGGTC[A/C/T]TAAATTAACTACTGG	10391
rs375418771	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68681527	CCAAATATTGGGATT[A/G]GGGGAGATAATCACC	10391
rs375462247	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68561486	CTAACTGGGGCCCAG[C/T]GGGACAGGTAGAGGG	10391
rs375514270	snp	C/T	3.35559e-05	0.00409595	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68725989	GCTCCCCAGCTGGGC[C/T]GTTTTCTAAGCCGAT	10391
rs375535253	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68673971	TTCGGTGGACCCAGA[A/C]GCAGCAGTAGGAGCT	10391
rs375554241	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68609575	ATCCACATCTCTTTT[G/T]GAGTTGGGGGAGTAA	10391
rs375560757	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68597204	AGAGGTGGCTTTGCT[C/T]GCCTGGCTGCTGGCA	10391
rs375572213	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608634	GGGTCAGGGAACATA[C/G/T]TCCCCTCTGCTTCCC	10391
rs375615938	snp	C/G	0.00044571	0.0149217	intron-variant	CORO2B	GRCh38.p7	15:68719107	GGCTTTCCCAGCAGC[C/G]CCCCATGTGTCCTCT	10391
rs375649523	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702821	TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	10391
rs375671179	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68670679	GAAGATTCACAAGCA[A/G]ATAAATGCAAATATC	10391
rs375686747	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703824	TAAAGATGAAGTTTA[C/T]GCTGCATTCCATAAA	10391
rs375725122	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68687495	ACAGCCTGCTGGGTG[A/C]GCCACACCCGTGGAC	10391
rs375757121	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722936	GCCAGGTGTGGTGGC[A/G]CACGCCTGTAATCCC	10391
rs375765518	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574116	GTGCAAGAGCTGCTG[A/G]GGGAGAACAGACTGA	10391
rs375873596	snp	C/T	0.000153988	0.00877328	intron-variant	CORO2B	GRCh38.p7	15:68725822	GGGCCCTCCTTGGCC[C/T]CCTCTCTTCCTCCAC	10391
rs375892839	in-del	-/TG			intron-variant	CORO2B	GRCh38.p7	15:68619666	AATGCTGGGTGTAAA[-/TG]TGTGTGTGTGTGTAT	10391
rs375929592	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68713393	GAAATGGCAGAGAAG[A/G]CATCTGTGGAGCCAT	10391
rs375976206	snp	C/T	0.00050452	0.0158747	synonymous-codon	CORO2B	GRCh38.p7	15:68710752	GATCTGGGAGATCCC[C/T]GAGGGCGGGCTGAAG	10391
rs375999690	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68666685	GGCACTGGGGGTTGG[C/G]GTGTTGTGTTGGGGG	10391
rs376035699	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68595814	GGGCAAACAAATACG[G/T]ATGAAGCCATTGGCT	10391
rs376041834	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668894	GACTAGCCTGACCAA[C/T]GTGCAGAAACCCCAT	10391
rs376044358	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68712004	CTTCAGTGCATACAT[A/C]CCCAGGTGTTACCCA	10391
rs376051456	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68637917	CTAGAAAATGCACCC[G/T]CTGGCCACAATAAAT	10391
rs376066447	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68684534	CAAGCATATACATGT[A/G]TATGTTGCGGACAGT	10391
rs376071859	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68589927	CTGGCAGTGCATGCC[C/T]TACATGCCTGGCTGC	10391
rs376095485	snp	C/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614665	TGTGCTGGAAAGTGC[C/T]TGGGAGGATTTCAGG	10391
rs376099601	snp	A/G	6.61518e-05	0.00575078	intron-variant	CORO2B	GRCh38.p7	15:68714682	GTAGGAGGTGGGGGA[A/G]GGCCCGGGGCAGCCT	10391
rs376134918	in-del	-/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68633380	ACGGATGTTTTCAAA[-/C]AAAAACCCATTGATT	10391
rs376136423	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68708346	TCTGCCTTTGGCTTT[C/T]TTTTTTTCTTCTTTT	10391
rs376141666	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68667960	AACGAGAGATAATAA[A/C]TCCCACCTGGCAGGG	10391
rs376159583	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68717842	TCATATTCACAATAC[A/G]GGGAAAGAAATGAAT	10391
rs376201699	snp	A/G	0.00122391	0.0247075	intron-variant	CORO2B	GRCh38.p7	15:68718820	CGGAGGGTAAGTGGG[A/G]CTGGGCTGGGCTCCA	10391
rs376219142	snp	A/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615507	AGAAGCAGAAGTGCT[A/G]TGGTTGAAAAATGTT	10391
rs376241230	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68612738	ACTCATGATCCTCAC[A/G]CCGCAGTCTCCTCCT	10391
rs376263216	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608060	CAGCTTTGCAGAGGC[A/G]TATGTCCTTTGACAC	10391
rs376283564	snp	G/T	0.000153988	0.00877328	intron-variant	CORO2B	GRCh38.p7	15:68719250	GTACCACAGCGGGGG[G/T]CTCCACAGAGCACAG	10391
rs376299069	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68607469	CATAGGGTCACTTCC[A/G]CACCCAGATTCCACT	10391
rs376335094	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68637811	TGTGAATGTAGCCAC[A/G]TTGCCCCCTCACCTG	10391
rs376354007	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68664893	TTATTGATGGAAGAA[A/G]TCCTTTATATGTTAG	10391
rs376355490	snp	G/T	4.53093e-05	0.00475948	intron-variant	CORO2B	GRCh38.p7	15:68710890	CTACAAGGTATGCAG[G/T]GGGCAGGCAGCTGGG	10391
rs376373471	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68579454	CCCCCAAGGACTGCG[A/G]AGGCCAGGGGGAGGA	10391
rs376383772	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68565713	ACTGGCTGGGAGAGG[G/T]ATTTGTCTATAGCCC	10391
rs376388273	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671379	TTGGCTGTAGACCCA[C/T]ATATGAGCCAAAGCC	10391
rs376391676	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68586829	TACCCCGATGCCTCA[C/T]GGAGCCTCCTTGGGC	10391
rs376411405	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68662150	TTTTCCTGTTATCAC[G/T]ACATTTTATGAGCCA	10391
rs376418407	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68677129	GCCAGGCCTGGAGCC[A/C]CGGAGGCACACCCTC	10391
rs376433753	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570690	TTACACTGAGGGGAA[C/T]AGTCAGTGTATTTCC	10391
rs376442381	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630629	GAATGCTTTAGGCTG[C/T]GAGTAACAAAGAAAG	10391
rs376473687	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68559346	GGACTCTCTCATTCC[C/T]GGAGAATTAAAAGCC	10391
rs376495186	in-del	-/ACA			intron-variant	CORO2B	GRCh38.p7	15:68624435	GCACGACTACCAACA[-/ACA]CAAATAACAATCGTG	10391
rs376526588	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68612443	GAAATGTCCAACACT[A/G]CAGAGGAGTCCTGGA	10391
rs376527946	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68562870	TAGAACCAGCTACTC[A/G]GGAGGCTGAGGCAGG	10391
rs376548791	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68716959	ATGGGGAGGGTTCTT[C/T]TTCTTGAGTGGGACA	10391
rs376583915	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68664302	AGATTGCAATAATTT[A/G]TATTTGAACCAGCAA	10391
rs376611595	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68673258	AAGAAAGAGGAGGTC[A/G]GGCACAATGGCTCAC	10391
rs376625577	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68717980	ACTGGAAGCTCAGAG[-/AG]TTGTAACTTGCCAAA	10391
rs376639486	snp	C/G/T			intron-variant	CORO2B	GRCh38.p7	15:68689719	TGTGGGACTTGGGGA[C/G/T]AAGATTGCTGACATT	10391
rs376640132	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68644365	GGACCCAGTAATCAG[C/T]ATTTCTTATAAATGA	10391
rs376683159	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68694334	TTAGCTCACATAATC[A/T]TCACAACAATGCTAA	10391
rs376740273	snp	C/T	1.64974e-05	0.00287201	missense	CORO2B	GRCh38.p7	15:68719479	TATTTAAGGCTCCCA[C/T]CAAAGAAAAGAAGAG	10391
rs376753952	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703016	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	10391
rs376778388	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68693650	TTCCACACCCATCCA[C/T]GCCCCTTGTTCCATC	10391
rs376793966	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68621076	AGCTTGGAGTGGACG[A/G]ATGAGATCGGCAGTG	10391
rs376799088	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648260	ATTGCTTGAACCCGG[A/G]AGGCAGAGGTTGCAG	10391
rs376802011	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68699444	AGATCAGTGGAGAGA[A/G]GGGAAGAGCGGAGGG	10391
rs376867263	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68633653	GGCAAGTTGATTTAC[C/T]ATCCTTTTTTATACC	10391
rs376890826	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68660664	TATGAGCCACTGCAC[-/T]CCAGCCAAGATTCAT	10391
rs376894903	snp	A/G	0.000149119	0.0086335	intron-variant	CORO2B	GRCh38.p7	15:68719268	CCACAGAGCACAGGC[A/G]GCTGCAGCCTTTGCC	10391
rs376902105	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68646294	CGCTTCAGGGAAAGT[G/T]CTTGCTGTCAGTCCC	10391
rs376906596	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68702407	CAGTAGATGCTCAAC[A/T]ATGCTTCCTTCTGGG	10391
rs376925309	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68717173	ACAAAAAGTACCTGG[A/G]TGTGGTGATACACCC	10391
rs376937957	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68711713	GTTCTGCAGGTGGAA[A/C]CCTACATTTTTTGAG	10391
rs376946458	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68708838	GTGCATGCCACAACA[C/T]CTGGCTAATTTTTTC	10391
rs376964613	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68666873	GTTCAGCGAGATCAG[C/T]GTGTTCAGGGTGGTA	10391
rs376993354	in-del	-/TC	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68705853	CTCTAACAGGTACAG[-/TC]TCTATTTTCTGGATG	10391
rs377024158	in-del	-/TTTCTTTTT	0.095934	0.196885	intron-variant	CORO2B	GRCh38.p7	15:68701298	GCGATCTAGGACTAG[-/TTTCTTTTT]TTTCTTTTTTTTCTT	10391
rs377026760	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68560112	ACTTGCACCCGTGCA[C/G]TGCTCAGGCATTGGC	10391
rs377033873	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68667237	CAGCCCCGGTCTCTT[C/T]TACCTGCCTGCCCTT	10391
rs377040217	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68636845	TCCCAGTGCTGTCCA[A/G]TGCAACACACTGCAG	10391
rs377101526	in-del	-/AT			intron-variant	CORO2B	GRCh38.p7	15:68565385	GATATATTCAAGTGC[-/AT]ATATATATATATTCA	10391
rs377144778	snp	C/T	3.92318e-05	0.00442881	intron-variant	CORO2B	GRCh38.p7	15:68718852	GAGGGGGGCCTGCAT[C/T]GCCTCTTAGCCTGCT	10391
rs377155298	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68657517	AATGAGATCCTGTCT[A/C]AAAAAAAAAAAAAAA	10391
rs377193285	snp	C/T	3.30617e-05	0.00406568	synonymous-codon	CORO2B	GRCh38.p7	15:68719224	TGAATGGCTGGGAGG[C/T]ATCAACCGAGGTACC	10391
rs377206138	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68568111	AATGGGGCCACCCCC[-/T]GGGGTTCCTTGTAGG	10391
rs377229246	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68678640	GATTGTGCCACTGTA[A/C]TCCAGCCTGGGCAAA	10391
rs377230404	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68696517	TCGTGCCACTGCAGT[C/T]CATGCACTCCAGGCT	10391
rs377245650	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68616956	GGAAAGGAAGGAACT[A/G]AAGTTTACAAACACT	10391
rs377262626	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68593763	TGAGTTTGCTCTGAG[-/G]TGGCGAAGTGGGTGT	10391
rs377262826	in-del	-/GA			intron-variant	CORO2B	GRCh38.p7	15:68588821	GGAAGGGGACAAAGG[-/GA]TTTAATTCCTGAGGA	10391
rs377264258	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640052	CTCTCTGGCAGAGTA[A/G]GGAGGAGTCTTTTCT	10391
rs377268193	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68583112	AGCCTTCCCTCTCCT[C/G]CCTCAGCTCCAGCAG	10391
rs377308851	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634041	CGGCAGTGGCAGCTA[C/T]GCCTGGCATCTCCCC	10391
rs377345424	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68575491	AGGTGCCCACCACCG[C/T]GTCTGGCTAATTTTG	10391
rs377347567	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68704696	TAAGAGCCGTTCCCC[C/T]GTATCTAATCTGTTT	10391
rs377355615	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68678758	ACCAGGCTCAGAAGA[A/G]CTGCCCACACCATGT	10391
rs377360009	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641110	CCAGTCCCAGCCTAC[C/T]AGCCACTGTGGAGAG	10391
rs377365890	in-del	-/AC			intron-variant	CORO2B	GRCh38.p7	15:68704476	GAAACTTGGGGAAAA[-/AC]TCTCACAGCCAATAA	10391
rs377374240	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68596758	GGAGAGGGGTACAAC[A/G]CAGCAGGCAGAGTCT	10391
rs377411673	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68597627	TGTTTCCCCCCCATC[-/A]AAAAAAAAAAAAATA	10391
rs377420578	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68581241	CCCAACAAACCCTCC[A/G]TGTCGCTCACCTCCT	10391
rs377437630	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725379	GTCTCAAAAATAAAT[A/G]AATACATAAATTAGC	10391
rs377512463	snp	C/T	1.66427e-05	0.00288462	missense	CORO2B	GRCh38.p7	15:68725960	AACTTGCGCAACAGC[C/T]CCAAGAACTGTTAGC	10391
rs377523920	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68626549	CAGAAGGGAGAAGCC[A/G]GGGGCTTGGCTGACA	10391
rs377533237	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68562094	CCTTAATGATGTTGT[C/T]CTCCAGCCACCCCTT	10391
rs377538576	in-del	-/GTTTGTTGTTTCTTGTTTTGGGTTT			intron-variant	CORO2B	GRCh38.p7	15:68625618	TCTTGTTTTGGGTTT[-/GTTTGTTGTTTCTTGTTTTGGGTTT]TTTTGAGACAGGGTC	10391
rs377599226	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68596310	GGACAGAACACAATC[C/T]TGACATCAGTGGTAG	10391
rs377601822	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68619871	GGACAATGCTGGCAT[C/T]GTCACTCTCATTTTA	10391
rs377603518	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68626852	CTGGGGCCCCAGCCC[C/G]CAGGCACCTCTCTGT	10391
rs377641781	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68673895	CACAGCACCGTGGGT[A/G]ACTAACTAGGAAAGG	10391
rs377644384	snp	A/T	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68653474	CCCATCTACTCTGAG[A/T]TGGGGTCTCTTCTTT	10391
rs377660490	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68657164	AGAAAAACCCATAGA[A/C]CCCTTCACAGAATAA	10391
rs377699065	snp	C/T	0.000153988	0.00877328	intron-variant	CORO2B	GRCh38.p7	15:68645390	CCTTCACTCCAGCTG[C/T]AGCTCCAGGGCAGAG	10391
rs377729731	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68689058	CCCGAGCTCTTCCTT[A/G]GGAAGACTCAGGGTA	10391
rs377731489	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68713654	TGCCTCCAGGGTCAC[A/G]CACCTTCTCCCCTGT	10391
rs386383368	in-del	-/TT			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630431	GAAATGTTTTTTTTT[-/TT]TGTTCCTGGCAGGGG	10391
rs386383369	in-del	-/AGG			intron-variant	CORO2B	GRCh38.p7	15:68658309	TTCAATGGAGGAGGA[-/AGG]GGGCGAGATGCATGG	10391
rs386383370	in-del	-/TT/TTT			intron-variant	CORO2B	GRCh38.p7	15:68660977	ATGTGTAATGAGTCT[-/TT/TTT]TTTTTTTTTTTCTGT	10391
rs386383371	in-del	-/CTTTT			intron-variant	CORO2B	GRCh38.p7	15:68665013	TTAAGTTTACCAGTC[-/CTTTT]TTTTATGGCTTCTGG	10391
rs386383372	in-del	-/TT			intron-variant	CORO2B	GRCh38.p7	15:68686021	GAGCTCCTACTTCTG[-/TT]TTTTTTTTTTTTTTT	10391
rs386383373	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68696558	CAAGACTCTGCCTCA[-/AA]AAAAAAAAAAAAAAA	10391
rs386383374	in-del	-/AAAAA			intron-variant	CORO2B	GRCh38.p7	15:68696570	TCAAAAAAAAAAAAA[-/AAAAA]AAAAGAATCCAGGGA	10391
rs386383375	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68709888	GGATGTTCCCCCCAC[-/C]CTACCACCTACCTTA	10391
rs386383376	in-del	-/TTAT			intron-variant	CORO2B	GRCh38.p7	15:68721752	TTTCTTGTATTTATT[-/TTAT]TATTTATGTTTTAGA	10391
rs386785042	in-del	AAT/CAGC			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640147	CCTTCTGCAGACACC[AAT/CAGC]TTTGGCCCACAGTGT	10391
rs386785043	in-del	AGGGT/GC			intron-variant	CORO2B	GRCh38.p7	15:68658312	CAATGGAGGAGGAGG[AGGGT/GC]GAGATGCATGGTGCT	10391
rs386785044	multinucleotide-polymorphism	AAAAA/GAAAT			intron-variant	CORO2B	GRCh38.p7	15:68663040	GTCGCTAAACTCAAA[AAAAA/GAAAT]TTCCAATTTATTGAA	10391
rs386785045	in-del	AA/T			intron-variant	CORO2B	GRCh38.p7	15:68682771	CAGAGCTGAGATGAA[AA/T]CCCAGGTCCCCTGAA	10391
rs386785046	multinucleotide-polymorphism	GCC/TCT			intron-variant	CORO2B	GRCh38.p7	15:68692840	GTTTTCTCCATGTTG[GCC/TCT]AGACTGGTCTCAGAC	10391
rs386785048	multinucleotide-polymorphism	AT/TA			intron-variant	CORO2B	GRCh38.p7	15:68708690	TCTTCCTTTTTTTTT[AT/TA]TTTTCTGAGACAGAG	10391
rs386785049	multinucleotide-polymorphism	CAC/TAT			intron-variant	CORO2B	GRCh38.p7	15:68711243	CCCGAGCCCCAGGCA[CAC/TAT]CCTCAAAAAAAGGTG	10391
rs386785050	multinucleotide-polymorphism	AT/CC			intron-variant	CORO2B	GRCh38.p7	15:68712826	TCGAATCTCACAGTT[AT/CC]AGGAGGAGCTAGGAT	10391
rs386785051	multinucleotide-polymorphism	CA/TG			intron-variant	CORO2B	GRCh38.p7	15:68715011	ACACACACACACTCA[CA/TG]TCAGCCCATCCACCT	10391
rs397698129	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68629814	AGCTTGGGCTCTTAA[-/A]CCAGCATGTGTGTGT	10391
rs397708940	in-del	-/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68670068	CTCAGAAAAAAAAAA[-/C]GGGGGGGAAAAATAA	10391
rs397753545	in-del	-/CTTTT			intron-variant	CORO2B	GRCh38.p7	15:68665017	GTTTACCAGTCTTTT[-/CTTTT]ATGGCTTCTGGATCT	10391
rs397756798	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68565323	TTTTATTTAAAAAAA[-/A]TTTTTATTGGCATGC	10391
rs397774659	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68562992	AAGAAAAAAAAAAAA[-/A]GAAAGAAAAGAAAAC	10391
rs397803659	in-del	-/TTAA			intron-variant	CORO2B	GRCh38.p7	15:68685774	TGTTTGATTGATTAA[-/TTAA]ACACTTTATTTTATT	10391
rs397819376	in-del	-/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68610721	TGCAGAGTAGGGTAC[-/C]TCTGAGGCCCAGTCA	10391
rs397854475	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68673837	GCGAGACTCCGTCTA[-/A]AAAAAAAAAAAAAAA	10391
rs397935802	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68669799	GGTGGCTCATGCCTA[-/A]TAATCCCAGCACTTC	10391
rs398027778	in-del	-/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68563499	TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTAAAG	10391
rs398027779	in-del	-/CT	0	0	intron-variant	CORO2B	GRCh38.p7	15:68608949	TTCTCTTTCTGTCTC[-/CT]CTCTCTCTCTCTTCC	10391
rs398027781	in-del	-/T	0	0	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640525	AATACTCCTATCACC[-/T]TTTTTTTTTTTTTAA	10391
rs398027782	in-del	-/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68696100	ACCACACCCACCTAG[-/T]TTTTTTTTTTTTTAA	10391
rs398043462	in-del	-/G	0.5	0	intron-variant	CORO2B	GRCh38.p7	15:68668287	GGCTGGGGAGGGGGG[-/G]CGCTACAGGGGATCC	10391
rs398057794	in-del	-/CT			intron-variant	CORO2B	GRCh38.p7	15:68559699	TTGGTGCAGTGCTCT[-/CT]GGGGTTCTCCCAGGG	10391
rs398057795	in-del	-/CC			intron-variant	CORO2B	GRCh38.p7	15:68656182	CGTCCCCCCCGCCCC[-/CC]GACCCAACCAACCCG	10391
rs527259043	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68628404	GCGCCTGCCTCACTG[G/T]GTTGCGATGAAGACT	10391
rs527283841	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635344	AAACCATCTGTTGGG[C/T]CTGTGTTTTGAGCTC	10391
rs527331520	snp	C/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68720483	TGGCTGAAGGTCTCT[C/G]ATGAGGGTACAGTTA	10391
rs527341995	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68641759	AGACAGAGTTCGGCA[C/T]TGTCGCCCAGGTGGT	10391
rs527349209	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68594693	ACTTCCCATGTCTGC[A/G]AGCCAATGAGCAGAG	10391
rs527356364	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68711275	GGGCTGACCACATGG[A/G]ACCTGACAAGGAACA	10391
rs527360158	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68587372	GCCCAGAGCGGTGGT[A/G]TGTGGAGGCTCACCC	10391
rs527382554	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68634962	GGAAGCACCTGGTGG[C/G]CTTGGTTAAAATGCA	10391
rs527387263	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68601594	ATCAGAAGGCCTGCC[C/T]CAGGGGTGGCCTGGA	10391
rs527397875	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594124	ACGAATAAACAAAAG[C/G]GGTGTTTGGGGGAGA	10391
rs527405857	snp	A/G	5.08048e-05	0.00503983	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726014	GCCGATCTCTCCGTC[A/G]TTTCTACTCATCCCT	10391
rs527418539	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641314	AAGTGCTAGCTGGGC[C/T]GTGGGGGCAACAGGA	10391
rs527424101	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681997	GACAGCTCCGGAGGG[C/T]CCAGTCCCAGCCCAC	10391
rs527441884	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68696189	TGGAAGGTCAAGGCT[G/T]CAGTGAGCTGTGATT	10391
rs527471845	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600763	AGGAAATGAAAACAG[C/T]AAATGGGACAGCCCT	10391
rs527504500	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68695359	CACCCTTTGCCCTTC[G/T]TCCCTCCTCTTTGTC	10391
rs527566121	in-del	-/AAT	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68660855	AGCTTTTTCTGTAAC[-/AAT]GATGGTATCTTCAAC	10391
rs527572865	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68564582	CTCCTACAGTGCCGG[A/G]ATTACAGGCATGAGC	10391
rs527581784	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558108	CGGGCAGAGAGGCTT[C/T]AGTAGGGCTGAGTCA	10391
rs527593905	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654170	TTTTTGGAAGAATGG[C/G]TGCTGATTTTTGAGG	10391
rs527594468	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68607064	CAAGCTCGAGATAGA[C/T]ATTGGGCTTTTGAAG	10391
rs527606743	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572348	TTTCACGTTACCTGC[C/T]GCTTGCCTTGCTTTT	10391
rs527616325	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563882	AATCAAGAATTCCCA[A/G]CAAAGAAAGGTCCAG	10391
rs527644121	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68691286	AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG	10391
rs527653151	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603293	ATTGAATGAATGAAC[A/G]AGTGGATGGATGGGA	10391
rs527674559	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603317	GATGGGAGGGTATGC[A/C]CAGATGAGCGAAAGT	10391
rs527676272	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595667	TATCACTAGACCAAT[C/G]CAAATCTTAATACAA	10391
rs527711474	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68610115	AGCTCCTCTTAGGTA[A/G]TAGGCATTGAACGAT	10391
rs527716340	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650739	TTCCCTTAGCTATAT[G/T]ATCTAAATTTCTTAC	10391
rs527730747	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68650158	CTGATCACCCGAGGT[C/G]AGGAGTTCAAGACCA	10391
rs527764394	snp	G/T	0	0	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615301	TTTCTAATCAAAGTG[G/T]ACAGAGAATCAGTCA	10391
rs527783522	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560198	GGCTGCTAACTGTGC[C/T]CCCTACAGCTGGTCT	10391
rs527800546	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68656284	CCTCACGTGTCAAGA[A/G]ACAGATCTGTGACAT	10391
rs527819528	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68668397	AATGAACAAGGGCGC[A/C]AACAGTCGTTAAGAT	10391
rs527821675	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68697241	ATGGATGGATGGATG[A/G]ATTGTTGGGTGTATG	10391
rs527821816	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566505	CAGGGATGCTGGTTC[C/T]TCCCCTTCCCTCCAG	10391
rs527822575	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68598382	GATAAATGGGAAGTT[C/T]TGCTGTCTCTGCTTC	10391
rs527853724	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68653153	GGGTCCTGGAGCAGC[A/G]GTCCAGACAAGATAG	10391
rs527886098	snp	A/C	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68702985	GCCCATGCCACCACT[A/C]CCAGCTAATTTTTGT	10391
rs527897751	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68708571	GTTTCTCCGTGTTAG[C/T]CAGGATGGTCTCGAT	10391
rs527912404	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574115	TGTGCAAGAGCTGCT[A/G]GGGGAGAACAGACTG	10391
rs527919202	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622851	ATTAGAATGATTCTC[A/C]TTGAACAGACTGGGA	10391
rs527930547	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68566557	AGTCAGGATACCCGG[C/T]GGACTCTTCATGGTC	10391
rs527941572	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68581759	AGGGTGTGAGAGGTA[A/G]GATCGCTGCTGACAC	10391
rs527954454	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622197	TAGTGGGTGCTCGGT[A/G]CATTCACGACAATTG	10391
rs527961396	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68715156	TGGCTCCTGGGACCA[G/T]GCCCTGCTCTGCCCT	10391
rs527974408	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68696076	CCCCCGTCTCTACAA[A/C]AAATTGAATTAAAAA	10391
rs528013795	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68649940	TGGGAAAATACTTTT[C/G]ACCCAATGGACTGCA	10391
rs528015577	snp	G/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68678146	GCACCCGTGCCACTG[G/T]CTGCTGGCTGTTCCT	10391
rs528040749	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580878	TCCTTCCCTGGAGGC[C/G]TGCAAGGAAGGTGTG	10391
rs528073536	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698832	TCATCTCACTCTTGC[C/T]CTGGAAACACCCCTA	10391
rs528074808	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68705031	TCCCAGCTACTCAGG[C/T]CCACTGTGAACTCCA	10391
rs528105534	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68633029	ATCTCTCTTCCCTCC[A/G]CTTATGGCTTCTGCC	10391
rs528133610	in-del	-/TCT	0.00914312	0.0669923	intron-variant	CORO2B	GRCh38.p7	15:68564306	TTCATAGCAGTGAAA[-/TCT]TTTTTTTTTTTTTGA	10391
rs528158838	in-del	-/CT	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68685434	CAGGCTGGTCTCACA[-/CT]CTCCTGAGGTCAGGT	10391
rs528162340	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68710538	CCCACAGGCAGAGAG[A/G]TGGTCTCCTTCCTCT	10391
rs528172693	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624209	CACTCTACCAATGTC[A/G]GCTATTAGAATCAGC	10391
rs528177455	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671666	TGGCAGGAGGCCTCA[C/T]TTCCTTGCAGGCTGT	10391
rs528193094	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68682753	CACTCAGCCAGTGTG[C/T]AGCAGAGCTGAGATG	10391
rs528194041	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68632876	GGATTACAGGCGTGA[A/G]CCACCACACCCGGCC	10391
rs528217708	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68706085	ACTCTGGGCCCAAGC[-/A]GGGCTTCTTCAAGCC	10391
rs528222728	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583434	AGTGCTCTTTCCACC[C/T]GGCTGCCCTGGCAAG	10391
rs528237438	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678373	GTGCCCCAGGCCTGT[C/T]GGGCAATAACAGAGA	10391
rs528239351	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671148	AAGAATGTTCAATGG[A/C]ACAGGAAAAGGAACC	10391
rs528275658	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582761	GTGATTTCCTGGCTG[A/C]TGGCTGTGATGTGAC	10391
rs528339970	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716032	TTCCCTGTGGGTCTG[A/G]TATTATGGACAGGGC	10391
rs528341553	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722455	AAGTGTGAGGAAACA[A/G]CTGACAGCTTGATGC	10391
rs528353503	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589444	AAACATTCCCTGTTG[C/T]TGCTTGGACAAAATC	10391
rs528354513	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684837	GAGCCTGGGACACAG[G/T]GAGCCCGATCTCTGC	10391
rs528395691	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643027	CCCATACTGTATTTT[C/T]CATACTGTATTTTTC	10391
rs528396998	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68596153	GTAAAGAGATGCGAC[A/G]AAGTCATTAGATTCC	10391
rs528407091	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727902	ACAGCTCCTTTGCCT[G/T]TCTGGAATGACAACC	10391
rs528427411	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684304	CAAGGAGAAATGGAC[G/T]AACCCAATGTCCCCC	10391
rs528462850	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68673500	TCTGGCCTGGGCACA[C/T]AGAGTGAGACACTGT	10391
rs528512470	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718111	CCCATGATAGACGTT[A/C]AGCAGAGGCAGCTGT	10391
rs528525870	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632305	ACAAGTTTGTTTCCT[C/T]TGAAGCTTGTCTGGT	10391
rs528532273	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591695	CCTGGGAGCTGGGTG[A/T]CACATATGCCCCACC	10391
rs528557315	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68584411	GCTCTCCAGGGCTCC[C/T]AGAATCACCCCACAG	10391
rs528566841	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591066	TCTCCAGGGGGATCC[C/T]GGTCTGTGGGGGGAC	10391
rs528573591	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68724564	ATATAGAATATTCTC[C/T]AGTCTTTTAGGGCTA	10391
rs528622260	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693433	GAAGGAGACAGCGGT[A/G]TAACCTCCTAGACTT	10391
rs528625071	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679180	AAGTGACATCCAAGG[A/G]AATCATCCCATCTTA	10391
rs528643514	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630219	GGCTCAGCAGTGTTG[C/T]TGGACCCAGGGGATG	10391
rs528646622	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578370	AGTCACTTCCCACGT[C/T]CGTCCCACTCTGATC	10391
rs528653125	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68597697	TCCATTGCTATGGAG[C/T]TCAGAGGCTTCACCA	10391
rs528673262	snp	A/G	0.000399281	0.0141238	missense	CORO2B	GRCh38.p7	15:68645356	TCGTCATCCCCCTGG[A/G]GCAGGTAGGTGGCCC	10391
rs528748781	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68652177	TGGCTGGCAGATCTC[A/G]AAGGAGTGGCTCTGT	10391
rs528810349	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651651	AGCAAACAGCAGGCC[A/G]CAGAGAATTGTCTCA	10391
rs528834427	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68616641	TGTGTCAGCGCGTGG[A/G]CCCCAGCGCAAGCAG	10391
rs528841491	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623982	CAGCTCAACCTCCAA[C/T]AAGAAGGAGGATTTT	10391
rs528854181	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68703791	TAACCAGACACCTCC[A/G]TAATCATGTACGCGT	10391
rs528856665	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68664107	AACTGGATGACAGAA[A/G]TATTCTACATTTTGA	10391
rs528857684	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671593	TGTCGGCCAGGGCTG[C/G]AGTCATCTGAAGGCT	10391
rs529010850	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68677130	CCAGGCCTGGAGCCC[C/T]GGAGGCACACCCTCC	10391
rs529025287	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68670074	AAAAAAAAAAGGGGG[A/G]GAAAAATAAAGAAAA	10391
rs529063384	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68596031	GAGGGTCGGGGGCTG[A/G]GAAGGTGATGAGGGC	10391
rs529064206	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68571921	ATGAAATGATGTAAC[C/T]GGGGTGGTGGTGGTG	10391
rs529064984	in-del	-/AT			intron-variant	CORO2B	GRCh38.p7	15:68565384	GATATATTCAAGTGC[-/AT]ATATATATATATATT	10391
rs529107085	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68636215	CAGGAGCAAGGGGAG[C/T]ACAGCATGGAATCTG	10391
rs529123225	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721377	CCTGAGGAAAGTGGT[A/G]CAGTGTAGGTGGGTG	10391
rs529126150	in-del	-/AATT			intron-variant	CORO2B	GRCh38.p7	15:68662022	ATAAATAAATAAATA[-/AATT]AATAAATTAATTAAT	10391
rs529150666	snp	G/T	0.000798403	0.0199641	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727867	GTCACCATGGTACCT[G/T]GATGGTCAGCTCCCC	10391
rs529164912	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68687905	ATGAGGGCACAGCCC[G/T]CATGACCTAATCACC	10391
rs529216399	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68602507	TAGGTCACTAAGAGA[A/G]AGATGAGCAAAAAGC	10391
rs529217380	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631728	CAGGAAATGCTGCAG[A/G]TGTTCAGGGGAGGGT	10391
rs529260746	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679088	TTCAGTAGATATTTA[C/T]TGAGACTCTACTATG	10391
rs529309541	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68722589	TAAAGCGGTTTTTTT[A/G]ACAAAAGTGGACCAA	10391
rs529316670	snp	A/C/G			intron-variant	CORO2B	GRCh38.p7	15:68622881	AAACAGGCTGGTGGT[A/C/G]GTGATGGTGATGGCT	10391
rs529317035	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68638600	AGCTACTGGGGAGGG[A/G]TAAGAGTTGAGGTGG	10391
rs529328503	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68644670	ATGACAGTGGATGGG[A/G]GGTTGCCTTCTTGCA	10391
rs529355840	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68604564	ATATGTGTGTGTCCT[C/T]CCCAGAGGACCACTC	10391
rs529364143	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68589998	CTCCTGGAAGCTGGC[C/T]GTCCTGGCACACTGG	10391
rs529426465	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652072	TGAGACGGCACAGCC[A/G]GGCATACAGTATGGA	10391
rs529443980	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604169	CGTCGTTCTTATCAC[C/G]TTCGCTTGTCAGTAT	10391
rs529446979	in-del	-/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68715446	AGTTGGAACAGAACC[-/T]GCAAGAGCTGGCCCT	10391
rs529479911	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610778	TTTGGGAGGCCAATA[A/G]GGCATCAGGCCAGTC	10391
rs529483304	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691954	CTCAGGGAACACTCC[A/G]ATGCAGCTTTTGCGA	10391
rs529494315	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68698720	GCCTCGGTTTTGCTC[A/G]TCTCTGAAACAGTAA	10391
rs529543741	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651536	ATTTGGACCATTTCT[C/T]GGTGACTGCAAATCA	10391
rs529559150	snp	A/G	1.9615e-05	0.00313163	missense	CORO2B	GRCh38.p7	15:68710777	CTGAAGCGGAACATG[A/G]CGGAGGCGCTCCTGG	10391
rs529562820	in-del	-/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68579460	GGACTGCGGAGGCCA[-/G]GGGGGAGGATGCCGC	10391
rs529571445	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575306	GCCTCACTCCTCTGG[A/T]TGCCTCCTGCAGTGA	10391
rs529572339	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664768	ACATTTTTATTAAAA[A/C]TGAGGTTGAAAATAT	10391
rs529580206	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561039	TGGCACACAGAGAGC[A/C]TAGAGCTCTGGTGGT	10391
rs529606215	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657679	ACATATTTTGAGTTA[A/G]TAGTAGCAGAAGTTA	10391
rs529617773	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68567849	AGATAGTGAAACCCC[A/G]TCTCTACTAAAAATA	10391
rs529647324	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68686831	TTGAACCCAGGCGGC[A/G]GAGGTCACCGTGAGC	10391
rs529694272	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563165	CAAACTAAACCCAAA[A/G]CAAGCAGAGGAAAGA	10391
rs529703270	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605959	TCAAACTCCTGAACT[C/T]GTGATTCGCCCACCT	10391
rs529712706	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693622	TTTGTAGCCGCTAAA[C/T]ATGGAACAGCTCTTC	10391
rs529739891	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68659886	TTGCAGTGAGCCAAG[A/G]CCTGGGTGACAGAGC	10391
rs529795102	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68715444	CAAGTTGGAACAGAA[A/C]CTGCAAGAGCTGGCC	10391
rs529803882	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618964	TTTATCTAGGAGAGG[A/T]TCACAGTGGCATCAG	10391
rs529812448	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68658521	GTTGCTCACTCTTGG[G/T]TGCTTAACTCTTTGC	10391
rs529849342	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68658118	TCTAGGCCTCAGTTT[C/T]CCCATCTGTAAAATG	10391
rs529856440	snp	C/T	4.95282e-05	0.00497611	missense	CORO2B	GRCh38.p7	15:68711627	GCATGTCCTTCAACA[C/T]GGACGGCAGCCTGCT	10391
rs529881146	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68625598	GTTTTTTTCTTGTTT[A/G]TTGTTTCTTGTTTTG	10391
rs529885402	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68598029	AGTGATGGAGAACCC[A/G]GGAGAAAGAGGTGGC	10391
rs529910724	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68705490	GAAAACCAGGACCCA[A/G]GGAGGGAAGTGGCTG	10391
rs529920091	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68568186	GCCACTGAGTCTTCC[A/G]GAACCTGCTTTACCA	10391
rs529927585	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68673418	GGCTACTTGGGAGGC[C/T]GAGGTAGGAGAATTG	10391
rs529928111	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68695805	ACCATTCAATGAGAA[C/G]AGAGAAGAAACAGGA	10391
rs529929138	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68576997	GGCAAGGAGGTGGTG[C/T]CGTGAGAGGTGGGAT	10391
rs529938314	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68716768	TGTGGCCAGAATGAG[C/G]CTGGCATGTTCTAGG	10391
rs529967426	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585162	ATGGGTTACTTCCCT[A/G]AATCCCATCAGCTCT	10391
rs529970513	snp	A/G	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68711290	GACCTGACAAGGAAC[A/G]TGTATCCTTCTTGCT	10391
rs529974014	in-del	-/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68592343	CTTGGATATACCCCA[-/C]CTGTGCTTGTTCTGT	10391
rs529993197	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68594841	AGCTTTTCAGCACAT[A/C]CTTTCCTGGCGAATC	10391
rs530032727	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701201	ACAGAGAAAGCAGCA[C/G]TATGGCTCCCTGGCT	10391
rs530044183	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706927	TGTGTTGCCCAGGTT[A/G]GTCTTGAACTCCTGG	10391
rs530048703	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571660	AATTGTTTATATAGA[C/T]ACAGGTCCCACACAC	10391
rs530050866	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68672658	CTGCAAGTGATACAG[A/T]GGCTCAGCTTTGGAA	10391
rs530055959	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68584253	ACTGTCTCTCCCTCT[A/G]GGCAATGAAGCTCAC	10391
rs530062522	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679893	TCGGAGGTGGTGCAT[C/T]TCCTTCTCTGGCCCC	10391
rs530072302	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621353	CATGGAGACCTGGAG[C/T]AAGCACGATGCAGGG	10391
rs530076205	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668718	GAAGCCATTGGAGGG[C/T]TTCAAGCTCAAGGTT	10391
rs530085509	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578956	CCCCTCTTCCTCCCC[C/T]CGCCCCCCAGCCCGG	10391
rs530107677	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712932	GCCATGAGCCCAGGG[A/T]AGGTGAAGGTCTTCT	10391
rs530183204	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578193	ATCAACACACAGGAC[A/G]CACCTGTGTTATCAC	10391
rs530190881	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68681274	GAAGACCACAAGATG[C/T]GAAGTGCACTAAATC	10391
rs530263560	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586470	GGATGAATGGGCAAA[C/T]GTCAGGAGTCAAAAG	10391
rs530280560	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68666932	TGCCAGAAACCTGCC[A/G]CATGCCCTTGGGTGA	10391
rs530282366	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626683	TGTGGGGAGCTCAAG[A/G]ATACAGAGGCTCAGG	10391
rs530289383	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640274	CCAGACCAGGTGTGT[A/G]CTCACACATTCCCCC	10391
rs530293415	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592454	AGTATTAACTGAGAT[A/G]GGGTATGAGAGAAAC	10391
rs530305321	snp	G/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68719052	GGAGAGCAGGTAGAG[G/T]GACTGGAGATCAGTA	10391
rs530310012	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68680866	ATGGGAAGCCCTCAG[G/T]AAATGACAGCCAGCA	10391
rs530336038	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688135	TATTTCTTCAAGAAC[C/T]GTTTGCTTGAAACCA	10391
rs530350269	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646367	CCCACTCCCACCCTC[C/T]GCCAAATCGCTCAGG	10391
rs530360985	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68655722	TCTTGAGACCCAAAG[A/G]AATGTGTTGGTAATA	10391
rs530363544	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718583	TCTGCATGGGCCGTT[A/G]CCTCCAAACCTAAGT	10391
rs530369127	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687544	TTCCAAGGGAGGGCC[C/G/T]GGCCATGGCTGCCTG	10391
rs530374659	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724846	CCTTCCAGGGCTCGG[C/T]GTTTTGTGGACATCT	10391
rs530377454	in-del	-/T	0.00239521	0.0345234	intron-variant	CORO2B	GRCh38.p7	15:68688208	TTGTAATAATATCTG[-/T]TTTTTTAATAACAAT	10391
rs530424746	snp	G/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68705421	CTAGCCTGGGCAAAA[G/T]GTGAAACTCTATCTC	10391
rs530446033	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562087	AGAAAGGCCTTAATG[A/T]TGTTGTCCTCCAGCC	10391
rs530468775	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68591291	AGGCAGATGAAGAGG[C/T]AGGAAAGGCATTCCA	10391
rs530518287	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68612062	AGGCAGGAGCCACTG[C/T]ACCCGGCCTCAACTT	10391
rs530521365	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68604957	TGTGTCTACTAAAAA[C/T]ACAAAAATTAGCCAG	10391
rs530524008	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68666048	GGTTGAGAAATATTT[C/T]CCCCCCAGCATTTTA	10391
rs530529830	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699627	GTACAGCCCTGAACC[A/G]CATCTTACCCGGGTG	10391
rs530552500	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611483	AGGAGCGTTTCCCCA[C/T]TGTATTATTTATACC	10391
rs530556966	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652221	CTTATTCGGGCTGCC[A/G]TTGTGAAGGCCAGTG	10391
rs530580043	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68624724	TTGAGATAGAGTCTC[A/G]CTCTGTCACCCAGGC	10391
rs530584133	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68672455	CCTGGCTAATTTTTG[C/T]GTGTGTACAGATGGG	10391
rs530590885	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68665202	TTCCCCCAGGTATCT[A/G]TCCAGTTGAAATAAT	10391
rs530623869	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68661018	AGACTTTTGCTGTCG[C/T]CCAGGCTGGAGTGCA	10391
rs530647208	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618092	GCTATAGTTGCTAGT[C/G]AGAAAAATCATTTTG	10391
rs530650017	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68718079	GTGCTCCTAGCACCA[A/C]CACACTGCCCCTCAT	10391
rs530659236	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568788	AACAATGGGAACACA[G/T]GGACACAGGGAGGGG	10391
rs530665111	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631630	CCAGCTTACAGCCTC[C/T]GGGAGAAGTTAATCT	10391
rs530681457	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617420	CCAAAGGACTTGGTT[C/G]TAGTCCCAGTTGTGC	10391
rs530686841	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68684197	GATGTCCTAGAAGTC[G/T]GCCTGAGAGTCTAAA	10391
rs530700874	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711210	AAGCTGCTGGAGGGC[A/G]AAAAGTGGAGCCTCA	10391
rs530709619	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68700364	CCCCCAGCCCTCCAC[C/T]TCCCTCTACTTGTCT	10391
rs530731229	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68702012	CTTTGGGAGGCTGAG[G/T]TGGGTGGATCACCTG	10391
rs530775818	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716945	ATAAGGAAATCATTA[C/T]GGGGAGGGTTCTTTT	10391
rs530816674	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630990	GTGGACTTCCTCCTA[A/G]GTCTCACTTGCCAGA	10391
rs530855434	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68712468	AAAGGAAATGCTCAT[C/T]GGAACATTTCAGATT	10391
rs530871623	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585627	GGCATGATCGTACTC[C/T]GCTTCCACTCCCCAC	10391
rs530894627	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674312	GGGGCTTCGGGACGG[G/T]GGGTAGTATATATTC	10391
rs530920970	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724756	TGTAATTCACACCAG[A/C]AAGTTTGAGACCAAA	10391
rs530957442	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585254	ATGACCACACCCTGG[G/T]CCCAGAGCTAATGTG	10391
rs530970490	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687505	GGGTGAGCCACACCC[A/G]TGGACTCACCATGCC	10391
rs530971900	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727123	CTAGGGATGCTCTGC[A/G]TGTGTCTCAGCACCG	10391
rs530987892	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577152	AGATTTAGTAAGTCC[C/T]TGGAACTCCCCTGGG	10391
rs530994045	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68585763	GTTGTGTCCTGCTTA[C/G]ATTTGCCTGTGGTCT	10391
rs531036590	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68558428	GCTGGAGTGCAGTGG[C/T]ACAATCACAGCTCAC	10391
rs531067516	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68645621	CACTCCCTTGGTGTA[C/T]ACAAGGTTCCATTCC	10391
rs531085503	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68704166	GATGGCTTGATCCTG[G/T]GAGGTGGAGGCTGCA	10391
rs531125919	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68652666	ACAGTAGTGTGGCCT[C/G]AGGAGCTTTTGAGGA	10391
rs531142088	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562756	AAGGCAGGTGGGTCA[C/T]GAGGGGTCAGGAGAT	10391
rs531172221	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639798	AAACCAATCTTGAAA[A/G]CCAATCTCAAAACCA	10391
rs531244247	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597838	GGCTGGTGTGGAGGC[A/G]TCTGACCCATTAGGG	10391
rs531254211	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68644972	GAAACCCACTAGAAC[A/G]GGCTGGGCATATGAG	10391
rs531254575	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68724843	CTGCCTTCCAGGGCT[C/T]GGCGTTTTGTGGACA	10391
rs531261821	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640923	AGTCTGAATGGGGAG[C/T]GGAGCCAGGACTGCA	10391
rs531282171	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68583052	ATAGATTGTAGGTCC[A/G]TGGGCAGCACGATCA	10391
rs531293561	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68681920	GGTTTAGGGGCTTCA[A/T]AGATTTAAAGGGCTA	10391
rs531305588	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68668816	GAGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC	10391
rs531325597	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68647147	AGCTACATGTGTATT[A/G]GAGGAAAATGGAGTG	10391
rs531337343	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68705834	TTTACTTGAACCCAC[A/G]CACCTCTAACAGGTA	10391
rs531354362	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68688875	GTCAAATGGATCTCC[A/G]GAGAAGGTGCCCTAC	10391
rs531389013	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561495	GCCCAGCGGGACAGG[G/T]AGAGGGTCCCCGGTT	10391
rs531391096	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68647704	CAAAAAAAAAAAAAG[A/G]AAGAAAGAAAGAAGG	10391
rs531397136	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68725616	GAATCAATTAATGAC[A/G]CAGGTTTTGTTTCCT	10391
rs531397295	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68694683	GACTGTGCCCTGGGG[A/G]AAGCAGGGAGTGTGG	10391
rs531409855	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701135	TGTAGAAGGAAGGTA[A/G]CCCTGAGGGGCCAGT	10391
rs531410509	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68619268	TGCCTTGCCTTAGAT[C/G]ACCTACCCTCACTTT	10391
rs531418477	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68589142	GACCTTTTCAGGGTT[C/G]GGATCCACATTAATT	10391
rs531434835	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68613596	CAATGACGCACAATG[A/C]CATGGACTTTTATTT	10391
rs531439821	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68654097	TCAAAGAGAAAAGTC[A/G]CAACTTTATTTCATT	10391
rs531441227	in-del	-/A	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68633032	CTCTTCCCTCCGCTT[-/A]ATGGCTTCTGCCTCT	10391
rs531445237	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68690335	ACACCCCTGCATTTC[C/T]TACTCTGGTTTTAGC	10391
rs531469225	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68706767	CACACTAAAGTGTAG[C/T]GGTGTGATCATAGCT	10391
rs531500658	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558070	AGGGCAGCCTGGCAG[A/T]GGAATGGCAGGGAGG	10391
rs531538220	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68557307	GAGCTGAGGTTCTGG[G/T]GCCAATCTATTCAAG	10391
rs531538740	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68570902	CCTCAGCCGCCCACA[A/G]TGCTGGGATTACAGG	10391
rs531549833	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68641720	GGGATGATTAGCCAC[A/C]TTTATTTTTTATTTA	10391
rs531563975	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68625886	CTGGGATTACAGGCA[G/T]GAGCCACCACACCCA	10391
rs531601887	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68559646	TTTTTCTTTCCCTAA[C/T]CCTTTCCCTGTCTGG	10391
rs531606444	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601804	GCTATTGTCTTAGTC[C/T]CTCTGTGCTGCTGTA	10391
rs531612655	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68566300	TTTGATAGGAGAGGA[A/G]ACAGGCCCAGAGAGG	10391
rs531626663	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571550	AAAATAAACAAATAT[A/G]TTACTACCTCTTTTC	10391
rs531627236	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68563254	GCACTTTGGGAGGCC[C/G]AGACAGGAGGATCCC	10391
rs531630578	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653647	CTGAATCTAGAAGTT[C/G]GTGGATCATTTAGCT	10391
rs531633796	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660701	AACCCTTCACTCCTA[C/T]ACACCTTTTTTACAT	10391
rs531645135	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668117	AGCTTATACAAAGTC[A/G]CACAGCTGGGAAGTG	10391
rs531653650	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68620947	CGAGCTCCACTTGGG[A/G]GCACAGCGAGCGGTA	10391
rs531686823	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655518	GATCCCAAAAAGGAG[A/G]AGTGTCTTATCCAAG	10391
rs531717588	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595057	CTTGATAGTATTTTA[A/G]GAGTCAGTTGAGTTG	10391
rs531723135	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697134	ATTGTGGATGGATGG[A/C]TGGATGGATTGTTGG	10391
rs531730852	in-del	-/AAAA	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68659922	TGTGTTTCAAAAAAC[-/AAAA]AAAGTCTATCCTCAT	10391
rs531741730	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702878	GGCACCCAGGCTGGA[G/T]TGCTGTGACACAATC	10391
rs531742548	snp	A/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68564751	CCTTCTAAAGTAAAC[A/G]GTCAAATCATATCAA	10391
rs531760110	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661733	TGTTCAGGGCCTGGC[A/G]TGGTAGCTCACGCCT	10391
rs531779259	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68675797	AATTTATTCACTTAA[C/T]AAATTTTTACTGAGC	10391
rs531808464	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702327	TAGCACTTATTCTTT[C/T]ATGCATCCAGCGCCA	10391
rs531815253	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68649257	TTTTCAACTTTATTT[C/G]TTCACGTGCTGTAAT	10391
rs531829033	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68628148	TTCAACAATAATGGT[A/G]CATTACCATAATGAC	10391
rs531855625	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621490	GCATTCCTGAAAGGG[A/G]ACCTGCCCAGGGTTC	10391
rs531861186	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68573266	AGAAAAGGCAAGAGA[A/G]ACAAAGAGAGAAAGA	10391
rs531870093	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642155	AATTCTCCTGCTTCA[A/G]CCTCCCGACCAGCTG	10391
rs531875890	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652334	CCTGATTGCCTGGCA[C/T]AGCTGGAGGGGCCTT	10391
rs531880293	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691903	AGATTTGCCTGGGCT[A/G]GGCTGGGTGCCAAAC	10391
rs531880672	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68605006	GTAATCCCAGCTACT[C/G]AGGAGACTGAGGCAG	10391
rs531885804	snp	A/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68623577	GCTGGAGGACCAGGA[A/G]TCATCTCAGGGCAGT	10391
rs531891839	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622144	TGAGAATTAAATGAG[A/T]CGAAGTTGGAGAAGG	10391
rs531892621	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618244	TTTTTTTTAAATACT[A/G]GTAGCAGCCTACCAC	10391
rs531893305	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627571	AAGGAGAGCCCGGCT[A/G]TAGCATAAGGAGCTC	10391
rs531899315	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668859	CGAGGTGGGTAGATC[A/C]CCTGAGGTCAGGAGT	10391
rs531907852	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68669310	ACTTGGAGCCTTTAT[C/T]TCTCAGGACACAACT	10391
rs531914285	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68693656	ACCCATCCACGCCCC[G/T]TGTTCCATCCGTTTG	10391
rs531958782	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580853	TTTTGTGCGCGAGCT[C/T]ATGCAGCCTTCCTTC	10391
rs531974418	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68714200	GAGGCCGAGCTTGGG[A/T]ACAGAGGCTTCAAGG	10391
rs531977799	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68656132	CCTTCCTCATGTCCC[C/T]GACTGCTGCCCACCC	10391
rs531978261	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68692906	CTCAAAGTACTGGGA[G/T]TACAGGCATGATCCA	10391
rs531995955	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580218	AACCCACACTCTTCA[A/G]AGAGATCTGTCTGGG	10391
rs532012497	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68628381	CCTGTGATATGGGGA[A/G]GATAATAGCGCCTGC	10391
rs532018572	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68676307	GGGTGAGGGACATAG[A/G]AGTCATGATGAGCTG	10391
rs532019038	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640329	CTTTACCAAAGCCAA[A/G]TAACTGATAATGGAG	10391
rs532019139	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647075	CAAGCAATACCTCAC[A/G]TCATGACAAAAATTA	10391
rs532032508	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646434	CTCAAAATTCACTGT[C/G]AGCTGGTGGTGGAGG	10391
rs532035889	in-del	-/T	0.172674	0.237741	intron-variant	CORO2B	GRCh38.p7	15:68625270	CGTGTCTTCAGCTAA[-/T]TTTTTTTTTTTAACT	10391
rs532091017	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587268	CCGAGCTCAGAGAAG[A/G]TGGATGTTTTACATG	10391
rs532112425	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68657925	GGGAAATATTATTGT[A/G]TAAAATCAGGACAGG	10391
rs532147784	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68707637	CAAGTTGAAAAAGAA[C/T]ATGTGTAATAGTATC	10391
rs532160086	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612852	GGGAGAGAAAGGTGA[C/T]AGTATCTGGTTTGTA	10391
rs532229562	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68713555	GGACTGTACTCCCTA[C/G]AGATGCTCTAGGAGA	10391
rs532247176	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712303	CACAAGAAGGGATTA[A/G]TGCTTGATCTGGGTG	10391
rs532281672	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68694083	TCAGGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA	10391
rs532283436	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563223	CCAGGCACCATGGCT[A/C]ACACCTATAATCCCA	10391
rs532307130	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68696503	GCAGTGAGCTGAGAT[C/T]GTGCCACTGCAGTCC	10391
rs532334441	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702134	AGGAAAAATCAGGTA[C/T]GGGCACGGGCAGGAG	10391
rs532346944	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700608	GGCCCGAGGGAGGGC[C/T]GGGGGCCATAACTCT	10391
rs532350227	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577099	AGGGTTTTGCACAGA[A/G]GAGACGCCTGAGGTC	10391
rs532359855	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68695529	AATTTAAAAATTAAG[C/T]GTGTGATTCAGCATT	10391
rs532371960	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68562833	ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG	10391
rs532395930	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577984	GCTGTCCTGCTTGGA[A/G]AACCCCTCTGCTTCC	10391
rs532401306	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662149	CTTTTCCTGTTATCA[C/T]GACATTTTATGAGCC	10391
rs532402754	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701719	TCAATCTCCTGACCT[C/T]GTGATCTGCCCGCCT	10391
rs532409649	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570153	TGGTAGGAAGAGCTA[A/G]GCTTGGAGTTGGATA	10391
rs532430815	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68654890	TACTGTTGTCTGGCA[C/T]AGTCCCTGAGTATGC	10391
rs532431600	in-del	-/AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA			intron-variant	CORO2B	GRCh38.p7	15:68650376	AAAAAAAAAAAAAAA[lengthTooLong]TGGAGACATTCCTGG	10391
rs532455095	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667072	CCCAGGCTCCCCGCT[C/G]CTGATCTCCCTTCAC	10391
rs532463833	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661571	AGGGTAGTCCTGATC[A/G]TAAACCTGACTACAT	10391
rs532484978	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68720851	ATAAAATGGGAGCCA[C/T]CTTAAACTAGACAGT	10391
rs532549287	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603446	CTGCAGCAACAGTGC[A/G]AGGTCATCAGCAGAT	10391
rs532580931	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68579346	GGCTAGGCTGCGGGG[G/T]GCGCGGGGGTGTGGG	10391
rs532586411	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614457	AGATGAGGAGCCTCC[A/G]GGCCAGCCAAGATTA	10391
rs532645526	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627190	TTTCATTTTTACTTG[C/T]TTATTTGTTTTACTT	10391
rs532676587	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621410	GAGAGGCTTCGCAGC[A/G]CTGGAGACATTTGAA	10391
rs532681246	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633817	ATCCCCTGGCTGTAA[C/T]GTAGATAGATTATCT	10391
rs532686246	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580100	ACCTTGGTCGGGGAG[G/T]GGTCCACTTTGGGCC	10391
rs532691210	snp	C/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630892	AAGGCGGGAAGCCGT[C/G]TGTGTGCCAGTATGC	10391
rs532703121	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68675393	TTCCTCTAGCTCACC[A/T]TCCCAGGGAAAGTAA	10391
rs532709941	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725356	CCTGGGCGACAAAGC[A/G]AGACTTTGTCTCAAA	10391
rs532712940	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68621066	TGTGTTACTCAGCTT[C/G]GAGTGGACGGATGAG	10391
rs532731014	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713551	AGCAGGACTGTACTC[C/T]CTACAGATGCTCTAG	10391
rs532746965	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68715940	GGTCCAAATCACCCA[A/G]TGAAACACCTATTTT	10391
rs532774793	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68620788	ACTCACTCAGCCAGC[C/T]GAGGCAGGACCAGGG	10391
rs532789117	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68634484	AGGAAAAATATGAAT[A/T]ATATCCATTTTTCTG	10391
rs532794983	snp	A/G	0.000116112	0.00761857	missense	CORO2B	GRCh38.p7	15:68725922	AGGACATCCGCATTC[A/G]GCAGCTCCAGCTGGA	10391
rs532796643	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68719662	TGAGACATTTTTCTT[C/T]CTGTGACAAATGCCA	10391
rs532871762	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68628579	TTACAATAGCTACAT[A/G]TATTAAGCCCATGGT	10391
rs532882672	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68629858	TGTGTGTGTGTTGTG[C/T]GCATACACACGCACT	10391
rs532885599	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68563267	CCCAGACAGGAGGAT[C/T]CCTTGAGCCCAGGAG	10391
rs532902874	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622920	TAGATACTTAGCACG[C/T]GTCTGGTGCTTTGTA	10391
rs532904324	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720585	ACTCATGTCCTCAGG[A/G]GCTATTGGAGTGAGG	10391
rs532913126	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68690535	CGCCTCTGTCTTCCC[A/G]GTACAGCATAGCACA	10391
rs532924797	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68638241	CTCCTCCTCCTGGCA[A/G]AGCCTGACCTCCTCA	10391
rs532933522	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68583729	TAGGTACCCAGGAGA[C/T]ACCTGAACCTCCAGA	10391
rs533023236	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677086	GTCCAAGACCTGTTT[C/T]TGCAGCACTTTCGGG	10391
rs533045816	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636070	GACAAACCCAGACGC[A/G]TCTGGAAATGGGAAT	10391
rs533086259	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68683290	GTTTGGGGTCCAGCC[A/G]TGGGAAGATACTGAA	10391
rs533093687	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68696270	AAAAAAAAAAGAGTT[C/T]GAGCATGGTGGCACA	10391
rs533098085	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68608388	ACACTGTGGTCCCCT[A/G]GAGGACTTCGGCCTG	10391
rs533107054	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558726	ATATAATAGGGGAGT[A/G]TGGACACGGGGTCAC	10391
rs533132761	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635480	ACTCCCATGGGATCT[A/G]CCTGCAGGGGAGGGG	10391
rs533139349	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642286	GGGTTGGGATTTGAA[A/T]CTAGGTGTGCGTGGC	10391
rs533156663	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68596906	CTGACCTGGGGCCCA[C/T]GGAGCCCATCCTGTG	10391
rs533172929	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68644807	TCCAGATACTCAGGA[G/T]GGAGTCTGTATGTGT	10391
rs533195101	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643972	AACCTGGGAGACGGA[A/G]GTTCCAGTGAGCCGA	10391
rs533202467	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68641795	AGTGGTGCGACTCAG[C/T]CCACTGCAACCTCCA	10391
rs533224737	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68651404	ATGTTGTTCCACACT[A/G]GCCGATTTTCTAGGA	10391
rs533243524	in-del	-/TGT	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68671255	ATTTCCCAATTTTTC[-/TGT]TGTTGTTTTTTTTTC	10391
rs533256018	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559378	CCGAGACATCCATTT[G/T]AGAAGTTCTGGTCAA	10391
rs533258629	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727920	TGGAATGACAACCCA[C/T]GTCTGTACCTACAGA	10391
rs533271221	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655429	CCCAGTCTTACATTG[A/G]CACAATGCCAGAGTC	10391
rs533272144	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68600829	CAGTCTGGTCCCCCA[C/T]GGGGAGACAAGAAGC	10391
rs533292377	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698675	ATTTACCATCTGGGT[A/G]GCCAATGGAGTGTTA	10391
rs533321605	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642184	TGGGATTACAGGTGC[A/C]TGCCACCATGCCTGC	10391
rs533326388	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68708026	AAAGGGGATGACAAT[A/G]GGGATGGGAAAATAT	10391
rs533345341	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610142	CGATGCAGAGATCTC[A/G]GGGAAATGGGCCTTA	10391
rs533387621	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684334	CAGTCCTCTTTGGAA[G/T]GCTTTTGTTTACTTG	10391
rs533392669	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609699	CCATTCTTCTTCCAG[A/G]ACATCCTGTGACTTA	10391
rs533411063	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68709278	TTACTCTGATTTATA[A/G]TACTACCAACATCCA	10391
rs533418103	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574762	ATATTTCATTATGAT[C/T]ATAATACAGGGTGAA	10391
rs533424176	snp	C/T	0.0879971	0.190408	intron-variant	CORO2B	GRCh38.p7	15:68703069	TGGACTCAAGTGATC[C/T]ACCCGCCTCGCATCC	10391
rs533435178	snp	A/G	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68596364	GGGCATGGGGGGTAG[A/G]GGGTGGGGGTTGTGA	10391
rs533436925	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68600789	GCCCTGGCCCAGCCT[C/T]CAGCTTCCTGGCCCT	10391
rs533448791	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656313	ATCAGCATCACATAG[C/T]ACTTCTTGTCTCCCC	10391
rs533461945	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68576425	AATTACATTTGGCTC[A/C]AGCTGCTATTAAGTA	10391
rs533469511	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616138	CAAGGACTGACTCTA[C/T]GGCCTGTGCTTTTGT	10391
rs533476129	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603414	CCTGAGACAGAGGAG[C/G]CTTCGTGGAGGACAA	10391
rs533479254	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68623408	GGGAGCCCTGGCAGT[C/G]TCCATGCATGTGGAA	10391
rs533482577	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650846	CAGAGGCCCTACAGG[C/T]CAGAGAGGGGCTCAG	10391
rs533506385	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68672748	GGAGAGGTGGAGAGG[A/G]AGGAGATACATCAGG	10391
rs533519119	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614221	AGAAACAAATCATCC[A/G]GATCTTTATTGTTAA	10391
rs533520556	snp	A/C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68643501	AGTGGGACAGGGACA[A/C/G]AGCATGGGCAAAGGC	10391
rs533528219	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68688616	TTTTACTAAGCGTAG[A/C]TCTTTAGCAATGCTC	10391
rs533574629	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703614	TTCTATACCATATAT[A/G]CAGACAGTGGGTACT	10391
rs533587522	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560383	CACTGCAGCCTCAAA[C/T]TCCTGGGCTCAAGCG	10391
rs533600396	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68719915	CTGCCTCCCTCGCTG[A/G]CGTTGCAGCAGTGCT	10391
rs533605405	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656901	GCCTGGCTCAGGGCA[A/G]ACCTTTCAGTGCAAG	10391
rs533618952	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68690939	AGTGGGATTACAGGT[A/G]TGAGCCACTGTGCCT	10391
rs533631088	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627342	AATGCACCAGGGCAG[A/G]GCAACTTGCCCTCAG	10391
rs533660098	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68663754	ACAAGACTTGAATAA[A/G]CATTGCATGAAAATG	10391
rs533662563	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68719290	GCCTTTGCCTTCAGC[A/G]CAGCTCACCCCAGTT	10391
rs533664734	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68670758	GCAAAGGAAAACAAT[G/T]AGATATTTTTCATCT	10391
rs533668380	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68670899	AGGCATCTTAAAATT[A/C]ATAACAAAAGCATTT	10391
rs533704119	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68705598	CCTGAGACCCTACAT[C/G]CAACAGTTCTTGGTG	10391
rs533725202	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574277	TGAGCTGAGGGGGCC[A/C]GCATGTGGGCATGCC	10391
rs533757602	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580355	GGCCAAAGTGGGACC[A/G]GCAGCCCAGAGTGGG	10391
rs533763494	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600049	AGAGGGAGTAGAGAC[A/T]GTTTCTGTGTGTAGC	10391
rs533768771	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707566	ACTTAAAAAGATAAG[A/G]TAGATATTCATGGAG	10391
rs533771723	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725701	ATAAATGCACCTGGG[A/G]AGAATAAATGTATCA	10391
rs533771789	snp	A/G	0.000111064	0.00745115	intron-variant	CORO2B	GRCh38.p7	15:68718840	GCTGGGCTCCAGGAG[A/G]GGGGCCTGCATCGCC	10391
rs533774541	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68592701	CAGCCAGCCCAGGCA[C/T]ACAGAGATGGAGAGG	10391
rs533797853	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68610050	AGAGAGAAAATGGAT[A/G]CGGTGACAATTCCAT	10391
rs533821382	in-del	-/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68639037	CAGAAGAAAGAACAT[-/G]GGTAGAGGAAGGGCT	10391
rs533832175	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68713743	ACCTGGATAATCCAG[A/G]GTAATCTCATCTCCA	10391
rs533845742	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68579481	AGGATGCCGCTCTGG[C/T]AGCCCCGGCGGTTTG	10391
rs533850008	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68675647	ACTCAAATAAGATGT[C/T]TATAGATCTATTTTT	10391
rs533860777	snp	A/G/T	0.00756386	0.061089	intron-variant	CORO2B	GRCh38.p7	15:68621164	AAGGCCATAAGCAAT[A/G/T]TAGCCACAGCGTCTA	10391
rs533870955	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68646916	CTGAATCAGATGGCC[G/T]CCGATCACTGTTGCC	10391
rs533900966	in-del	-/AGTA			intron-variant	CORO2B	GRCh38.p7	15:68691998	ATGACTCTGTCAGAG[-/AGTA]AGTGAGCTGTGGAAG	10391
rs533917749	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68675113	TTGTTCTCAGCTCCG[G/T]GAGCCACACTGAAAT	10391
rs533930343	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674645	CCCTGACCGCCAGAG[A/C]AAGGCTCGTGGGCAG	10391
rs533970671	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727387	TTTCATTTCCCACTA[C/T]GCACAAAGAGTTTAT	10391
rs533980607	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593249	TTGGCAGAGATATTC[A/G]AACCGTAGCCATGGG	10391
rs533994904	snp	A/C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681127	CTGAGGCAGGAGAAT[A/C/T]GCTTGAACCCAGAAG	10391
rs534038604	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68713312	AGCTCCTGAAGTGGT[A/G]TAGCCCCCAACTGGA	10391
rs534041100	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68648975	CATTTTTTAGTACTC[A/G]ATTATTTTTACAAGC	10391
rs534048062	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68641512	AAGGGGGAGGGTGGA[C/T]GAGGAAGAGGTGAAG	10391
rs534068052	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68559722	CTCCCAGGGGGACTG[C/T]CGGTGAGGCTGCGGC	10391
rs534079839	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68647220	CCAGGAATCCCCCAA[A/T]TCATAAAGGAAATGA	10391
rs534088551	snp	A/G	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68608801	TGGCTTTGAAGAGTT[A/G]TGGGGCTCCAGGAGG	10391
rs534121469	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689290	CTGAAGTTCTCTGAG[A/G]TTCTCTAACCAGATG	10391
rs534126987	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68694737	CAGCATCTGAGCGTG[C/T]GTGAACAAGGCAGAT	10391
rs534149157	snp	C/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68648217	ATGTGCCTGTAGTCC[C/G]AGCTACTTGGGAGGC	10391
rs534151153	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655800	CCAAGCCCCTCAACA[A/G]GAGGCCAGGTAGAGA	10391
rs534159253	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68628846	ATTGCTGGGTACAAG[A/G]GGCTTTCTGCTGAGA	10391
rs534188345	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588120	CAGGAAATGGTTTAT[C/T]GTGATGTCTAATCTG	10391
rs534210955	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635595	GGGTCTATGAAATGA[C/G]AGGCTGGATTTAGTG	10391
rs534220841	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68647020	CTCAAACCTATCGCC[A/G]GCACCCTGCCATGCT	10391
rs534231340	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68581604	AAGACTTGGTTCCAA[A/T]GATCTCTAGGGCCTC	10391
rs534250291	in-del	-/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68701635	GGACTACAGGTGCGC[-/G]CCACCATGCCCGGCT	10391
rs534260086	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68621174	GCAATGTAGCCACAG[C/T]GTCTAATGAGCAATT	10391
rs534274385	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603628	AAGGCAGAGCCCTGG[C/T]CCAGTAGGACTGGTG	10391
rs534291764	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726185	CTGGAGACCCCCTGC[C/T]GGCAGCCCCTTTCCC	10391
rs534304476	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594434	CTCACCAGGTTCCCC[A/G]GCCCAGGTGAGCAGC	10391
rs534306444	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601870	TGATTTCTCATAGCC[A/G]TGGAGCCTGGGAAGT	10391
rs534317778	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691775	GCTCCTCTCTGTTCT[A/G]AATAGGTTCCGGTGA	10391
rs534325016	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68573736	GGAATTACTAAGTGA[A/C]AGAGCCAGTCCCCGT	10391
rs534329200	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698297	TAACAGATGAGCAGT[A/G]CCTGTCTTGATGTAG	10391
rs534337238	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68565974	GTTAATTGGTGCTAA[C/T]GAATTCCCGCAGCCC	10391
rs534362619	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68592976	AGTTTATTTGGCTCA[C/T]GGTTCTAGAGACTAA	10391
rs534363197	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610341	CACTTGCCTCAAGGC[C/G]TAGTGAAGGGCTGGG	10391
rs534376399	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568034	AAAAAGAAAAGAAAA[G/T]AAAAGAAATATTGGC	10391
rs534376602	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68623789	ATCCCCGTTTGTGCC[A/G]CTTGCAAAGCATGAG	10391
rs534387024	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68590974	GACTGAGATTTATTT[-/A]AAAAAAATTTGCTGA	10391
rs534388166	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697442	AGAAAGAAAGATTCA[C/T]AGTAAATAGCCTCCA	10391
rs534393001	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68703855	ATGGAAACAAACTTC[A/G]TATCATATGTATTGA	10391
rs534413640	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68596200	ATTAAGCATGCACTG[A/T]GCCCGTGACCCTAGG	10391
rs534448024	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608271	ATCAGGGCTTGGCCT[C/T]CTGTGGCTGGCTGCG	10391
rs534456965	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68599744	GTGTGCCCTCCCCAG[C/G]CTCTCCCCTCCCCTG	10391
rs534482993	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614620	GAGGAAAGCCCCGGA[C/G]CCCTCACGGTCAAGG	10391
rs534496037	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703232	CTCAGCTCACTGCAA[A/C]CTCCGACTCCCTGGT	10391
rs534504019	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709536	GATCTCAGCACACTG[A/T]AACCTCCGCGCCTGG	10391
rs534507690	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661777	TTTGGGAGGCCGAGG[A/C]AAGTGGATCTCTTGA	10391
rs534511045	in-del	-/C	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68558364	AGCAAAAACTCCCTT[-/C]CCCCCTCACCATTTT	10391
rs534548300	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572710	CTGGTTTGGGGCCCA[C/T]ACTTTGAGAACTGCT	10391
rs534584846	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68602283	CCACTCTGACATGTA[-/T]TTTTTTTGATTAGTA	10391
rs534627680	snp	C/T	0.000132435	0.00813634	intron-variant	CORO2B	GRCh38.p7	15:68714687	AGGTGGGGGAGGGCC[C/T]GGGGCAGCCTGTGGG	10391
rs534630739	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651092	GTGGGTTACTGACTC[C/T]GTGGGAGGGTGAGGC	10391
rs534642865	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68677262	TATTTGCAGGGTGCA[C/T]TGCTGGTCATTCCCA	10391
rs534668973	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68658647	GACCTTGGGCAAGTT[A/G]CTTAACCTCCCTGAG	10391
rs534678036	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560474	TAATTAAAGACAATT[C/T]TTTTTGTAGAAACGG	10391
rs534686829	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705219	GTACAGTGGATCTCA[A/C]TTGAGGTCAGGAGTT	10391
rs534694780	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609873	TGGGGTAGGGGAGCA[C/T]GAAGCGGTCTGGTTC	10391
rs534696260	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68650455	CGTCTCCACTAAAAA[C/T]ACAAAACTTGGCTGG	10391
rs534716621	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656449	GGGGTAGTGCTTAAA[A/G]CTCTGCAATTTATAG	10391
rs534734414	in-del	-/A	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68567654	CAATGTTTTCAACTC[-/A]AAATAATTAATACAC	10391
rs534738106	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68703336	TTGTATTTTTAGTAA[A/C]GACAGGGTTTCACCA	10391
rs534750002	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711376	TTTGTGTGCCAGGGA[C/T]GTATCAGCCTTTCCA	10391
rs534769840	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68653887	AATGCCTGAATCTTC[A/G]TCACTGCTCTGCAGT	10391
rs534779290	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68663303	AGCCACATTTTGCCT[A/G]TTGATAAGTATTTCC	10391
rs534781345	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616225	GAATTATCACTGGAG[C/T]CTTCTCATAATAATA	10391
rs534813555	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68659724	AGATCACCTGAGGTC[A/T]AGTGTTCAAGACCAG	10391
rs534822697	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68664563	GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC	10391
rs534855130	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68709597	GAGTAGCTGGGACTA[G/T]AAGCGTGCGCCACTA	10391
rs534859007	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678575	GCTACTCAGTGGACT[A/G]AGGCAGGAGAATCAT	10391
rs534865693	snp	A/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68708690	TCTTCCTTTTTTTTT[A/T]ATTTTCTGAGACAGA	10391
rs534899764	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68677256	TCACTATATTTGCAG[A/G]GTGCACTGCTGGTCA	10391
rs534916929	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637978	TTGCTTCCATGTGGA[A/G]TGTACATAGTGATTA	10391
rs534976399	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68611165	GATGATGGAAAAGAA[C/G]AATGCAGAGTCTGGA	10391
rs534979991	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722208	ATCAAGCAATATTTC[A/G]CTGTAGACTTGCCTA	10391
rs534984761	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68658244	GGGTCGGTAGGAGCC[C/G]TGGACCAGGGAGAGG	10391
rs535004632	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68596599	CTCACTAATACTTCT[C/T]GACTGACTGGGAGGA	10391
rs535068266	snp	C/T	3.96032e-05	0.00444972	missense	CORO2B	GRCh38.p7	15:68710768	GAGGGCGGGCTGAAG[C/T]GGAACATGACGGAGG	10391
rs535093066	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575721	CCCAATCTTCCACTC[C/G]TGTGATCACCTTCCA	10391
rs535096407	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68683575	GCACCACCCCTCCCC[A/C]CACTGTAGGATATTG	10391
rs535116460	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68719390	GGGATCGTCAGTGAG[A/G]GCGTTTCCCTTGCCT	10391
rs535117743	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566829	CCCTTGGCATTGATT[C/T]AGTAGCTCCCAAAGC	10391
rs535123070	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68706172	CTCCACACGAGCCAG[A/G]CTGACCCCCGTGCAG	10391
rs535146837	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702475	GGATTCGTTTCCCAT[A/G]TTGGCAAACAGTGAG	10391
rs535148749	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68708643	CTGGGATTACAGGCG[C/T]GAGCCACCGTGCCTG	10391
rs535153796	in-del	-/TCATCC	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68717564	TCAGAATGACTCACT[-/TCATCC]TCATCCTCATCCTCA	10391
rs535161184	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68672092	CCACTTGTTCGCTGA[C/G]TGCAGCATGGGGAAG	10391
rs535186777	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68663163	ACATTGTTCTCTCTA[C/T]ATCTTGCTTTTTTAC	10391
rs535197956	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68558917	ACCGCGGGGAGGTGT[G/T]GTGAGAAATAAAATG	10391
rs535216234	snp	C/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68583167	GTGGCTCCTGCTGAA[C/T]GTGAAAGGACTGAGG	10391
rs535230971	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630411	GATGAGAGAAAACCT[C/T]GAAATGAAATGTTTT	10391
rs535252283	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589617	ACTGGGGCTCCCCCA[A/G]GTTACTGCTCAGGTT	10391
rs535254679	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708297	ATTCCCTGAGGGGCA[C/T]CCCAGTTCCTAGCCT	10391
rs535263027	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68700767	TCGGTTTCCAAGCCT[C/T]GTGCTCCCAGCCCTT	10391
rs535270710	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68572974	CCACACATGCACACA[A/C]ATGCACAGATACATA	10391
rs535286297	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644093	CAAAGTATATCAGTT[A/G]CAACAGGCTAGGATA	10391
rs535296033	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621888	CAGCCTCCCAAGGAG[C/G]TGGGACTATAGGCAC	10391
rs535305018	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68719763	GGTTCCCCACACCAC[C/T]CCCACGCCTCAAATT	10391
rs535309998	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68669212	AGCAAGCAAGCAAGC[C/T]GGAGACAGGACTCGG	10391
rs535325081	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68637354	ATGGAAACATGTGCT[A/G]TGTTCCTCCTGTGTG	10391
rs535329350	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68728155	CTCCCGGTTAAGAAC[C/T]ACTGTTCTACCGCTA	10391
rs535342886	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721223	AAGACCCTTCTTGAC[C/T]TCTGGGACCTCACAG	10391
rs535346839	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68714079	GGGTTTGGGCTAAAG[A/G]AAGCATCGTTGCCTC	10391
rs535353687	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68684486	GAGCTTGTATGGCAC[A/G]TACATATGTGTGTGT	10391
rs535358089	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68633871	CCAGTTACCACATTC[C/T]CCTGGGGACAGTTTA	10391
rs535372742	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587598	ACCAGGTGCTAGGCC[A/C]CTGCTTTCAAGGGAC	10391
rs535415760	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68656407	CAAGTGGGTCGTCAG[A/G]TGAGCATGAGAGGTG	10391
rs535425661	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68697358	TGTATGACAGGTGGG[G/T]AGATGGATGAATGAA	10391
rs535426254	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624317	CCAGGGAGTTTGAGG[A/C]TGCAGTAAGCTATGA	10391
rs535456536	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559789	CCACCAGGGGGCGCG[G/T]CCCGCATCCTTCCTC	10391
rs535464866	snp	C/T	3.05022e-05	0.00390515	intron-variant	CORO2B	GRCh38.p7	15:68710694	AAGGGACTTCTTGGC[C/T]GTGTCCACCCAGCCT	10391
rs535467747	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68562098	AATGATGTTGTCCTC[C/T]AGCCACCCCTTCCCA	10391
rs535483420	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68661702	GAACAGGGCACTTTC[A/G]TCTGCATTAAAAACC	10391
rs535530583	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656027	CTGGCCTTTCTCCTG[A/G]CAGCTTCCAGAACAA	10391
rs535544985	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630364	CAGGCACGGGCAGCC[A/G]CATCAGCACACCCCA	10391
rs535577547	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68722015	ACTTTCGCCTCCCAA[C/T]GTGCTGGGATTACAG	10391
rs535577880	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68573760	TCCCCGTCCTCAAGC[C/T]GGGGATGCTTCATTC	10391
rs535588888	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589605	GGCTGAGTGGGAACT[A/G]GGGCTCCCCCAAGTT	10391
rs535594299	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662597	GAGATGAATTGAATC[A/G]TATACATGGAGATGA	10391
rs535594366	in-del	-/ACA	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68661549	GGAGTTAGCAGCTTT[-/ACA]GATAAGGGTAGTCCT	10391
rs535604214	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68622416	TTGGTATGGGGTGAG[C/T]TAGCCTATAATTCAC	10391
rs535630654	in-del	-/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68680253	ATAGACTGGCATTGT[-/G]TTTGAGACCAGAGGG	10391
rs535641329	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68668574	GAGTAGTGCCCTAGA[A/G]AGAGAGAATAGCATG	10391
rs535649091	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68635805	GATCTGGAGCTCCAA[C/T]GGGACTCTTGTAGGC	10391
rs535660351	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68676525	CCATACACTGTCCCT[A/G]TTCCCCTGTGACATG	10391
rs535703094	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720727	GCACCCAAGATGGAA[A/G]CTACAGTCTTTCTGT	10391
rs535738618	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68627853	GGTGTATCCTCATCT[C/T]CACGCCTCCCTGTAT	10391
rs535740387	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635523	ATTCTACCACCCCCA[C/G]GGCAGGAAGCTTGCA	10391
rs535760361	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68602761	GAGGTTCTGTGCAAT[A/G]TGCAACACCCACTTT	10391
rs535773253	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606930	ACTGTGGATTGACTC[A/G]GAACCAGGAAAGGGG	10391
rs535777825	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635025	CTGCAGGCTGGAAGT[A/G]GGGCCCGGGAGCCTG	10391
rs535782691	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630848	AATGGGTGCCAGAGC[A/G]CCAGGATTTACATCC	10391
rs535802196	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664516	GCCGGCCATGGTGGC[A/G]GGCACCTGTAGTTCC	10391
rs535810405	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68617109	GTTGGGACTGAGACA[A/G]AGCCAGGTCTGTCAG	10391
rs535846725	in-del	-/TAA	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68725426	TATATGTAATACATG[-/TAA]TAATACATCTATTAT	10391
rs535859995	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68591321	AGGTTGAGCGGGCAG[C/T]GTGAACAAAGGAATG	10391
rs535862791	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671318	CTGGAATGTCAGGGA[C/T]TGTGCCCACAGTTTG	10391
rs535904190	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68639111	CAGCACATCAGCCTG[A/C]AAATAAAATGCAAAA	10391
rs535906410	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716472	GTACCAGACCCTGCG[C/T]GAAGTCCAGTGGCAA	10391
rs535916068	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583057	TTGTAGGTCCGTGGG[C/T]AGCACGATCAACTGT	10391
rs535949430	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68642766	GCTGTCTGCGGATTC[C/T]GAGAAGGTCACTGTG	10391
rs535954619	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652304	TTAAGCTGCAGATGG[G/T]GGAGCAATCAGCACC	10391
rs535975765	in-del	-/T	0.0154538	0.0865337	intron-variant	CORO2B	GRCh38.p7	15:68708537	GCTAATTTTTTTGTA[-/T]TTTTTTTAGTAGAGA	10391
rs535986778	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678025	GGCCCAGGAGGCTGC[C/T]TTGCCCCTCCATAAT	10391
rs536011036	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651902	ATGATTAAAAATTCT[A/T]CTGCAGAGTAGGAAG	10391
rs536069300	snp	G/T	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68678533	ACAAAAATTAGCCAG[G/T]TGAGGTGGTGGGTGC	10391
rs536072702	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595874	GGGACCCTGGTGAGA[C/T]GGAGCGGGCGTCTGG	10391
rs536110310	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68568816	GGGAGCAACACACAC[G/T]GGGGCCTGCCAGCCA	10391
rs536136849	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617520	ATGAAGGGTAGTGTG[C/T]GTGTGTGTATGTGTG	10391
rs536142864	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642736	TCTAGACTAGGAGCC[C/T]AGGGAGAGGCGCCGG	10391
rs536177360	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691039	TGTCTCTATAGAAAA[C/G]TGGTTTTCGGCCAGG	10391
rs536178385	snp	A/G	0.000199797	0.00999292	intron-variant	CORO2B	GRCh38.p7	15:68725809	CCTGCTCTCTCCTGG[A/G]CCCTCCTTGGCCCCC	10391
rs536180693	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68560442	TGGGACTACAGGTGC[A/G]TGCCACCATGCCCAG	10391
rs536185306	in-del	-/CAAGAGTGAAACTCCGTCT	0.0399052	0.1355	intron-variant	CORO2B	GRCh38.p7	15:68723048	CTCCAGCCTGGGCAA[-/CAAGAGTGAAACTCCGTCT]CAAAAAAACAAAAAC	10391
rs536193836	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657441	AGCATCACTTGAACC[C/T]GGGGAGGTTGAGGCT	10391
rs536203845	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699311	ATCAGTGGACCCCAC[C/T]GAGTGTGGTGCATGG	10391
rs536254699	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700735	GGGCGGCTGGCAGGC[A/G]GCAGGGAAGGGCGCT	10391
rs536266042	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703298	TGGGATTACAGGCAC[A/G]CGCTACCACGCCCAG	10391
rs536278567	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68598044	AGGAGAAAGAGGTGG[C/T]GCTGATTTCTCCACC	10391
rs536284820	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68723523	GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT	10391
rs536308794	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68562911	GAACCCGGGAGGTGG[A/G]GCTTGCAGTGAGCCG	10391
rs536326661	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68694007	TGCCTGCTTAATTTT[A/T]GTATTTTTAGTAGAG	10391
rs536361854	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597368	GGGCAGTCCTAATTG[G/T]TTTACACGCACCTCA	10391
rs536369183	snp	A/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68651474	CCTCAGTTTGATAGA[A/C]ATTTCCCTGAAAACA	10391
rs536376198	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68685502	CAGGCGTGAGCCACC[A/G]TGCCCAGCTGATAAT	10391
rs536409792	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68619352	TTTAGTATGATGCCT[C/T]AGAGAAGGATGTAAA	10391
rs536418200	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68566524	CCTTCCCTCCAGCCT[C/T]GGGACATGCCTGCTG	10391
rs536430750	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68712541	TGAATATTCTGACAT[C/T]GGAAACAATCCAAAA	10391
rs536435207	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705903	ACAGGTTAACTGGCT[G/T]GTTCACAGTCACTCA	10391
rs536436401	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577577	AAATAAAAAATTAGC[C/T]GGGCGTGGTAGCGCG	10391
rs536499774	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68561261	TCCTGCATATGCCAC[G/T]CTGGGCGGCCCCCCT	10391
rs536523324	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576706	CTGCCCAAGACAGCT[A/G]AGACAGGGAATCTGA	10391
rs536527555	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68673692	AAATACAAAAATTAG[C/T]CAGGCGTGGTGGCAT	10391
rs536532920	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68709414	CTGTTTTTCTCCTTA[C/G]TAGCAAGGGTGGAGT	10391
rs536543885	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68624203	AGGCACCACTCTACC[A/C]ATGTCGGCTATTAGA	10391
rs536576783	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68596829	CGGGGAGAAATGGCC[A/G]CGCATCACGCAGAGC	10391
rs536583018	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68626340	GAAAAATCAAAGAAG[G/T]CTAGGTTTTTCTTAA	10391
rs536621539	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653784	CCCAAAGCCTTCGTT[C/G]CCATTCCAGATTTCT	10391
rs536670293	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68646203	TATAACAGATTAAAT[C/G]TGAAAAACCTAGATC	10391
rs536693695	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68613101	TTTCTGGAGAGGTCC[A/G]GAAGAGGCATGTAAT	10391
rs536713683	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698889	CCCCACCCACCAAAA[C/T]GTGGTGCAGAATGAG	10391
rs536734684	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653119	CAACAATTCTAGTTG[G/T]CAAGGAGAGGCAGGG	10391
rs536735420	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660146	CAATTCTCCTTTGAC[C/T]ATGTGCCTGTATCAT	10391
rs536740579	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561582	GACAGCTGGGTGGGA[A/G]GGTGGAAGATGGACA	10391
rs536742283	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651727	ATTCCTTGCTTGCTT[C/T]TCTAAGAGATTTGGA	10391
rs536759276	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657977	TTGGTGGGGAGGGAG[A/C]AATGCAATAGACCTG	10391
rs536813919	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658612	GCCCTAGGTCCACCC[A/G]AGCTGCTTAATGGCT	10391
rs536826174	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704450	ATGAAGACAGATGTT[C/T]GGAGAGGCTAAGAAA	10391
rs536840980	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68712635	AAGAATAATGAGAGT[G/T]GCTTAGCATGATTAG	10391
rs536848050	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68651780	CAGGATCCCCAAATC[C/T]CTGCCCCGAGGCCAC	10391
rs536928977	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623727	GGGTGGGAGGGCAGG[C/G]AGGGCTGGGTGAGGA	10391
rs536931560	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68666595	AGAAAGAGAAGTGGC[C/T]TGAGCAGGTGCTTCC	10391
rs536936302	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68632550	CCTGCTTTAACAGTC[C/T]GAACTCTCCCTGGAT	10391
rs536994006	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671233	ATAGGAATTATTCTT[C/T]CTCTGTATTTCCCAA	10391
rs537028820	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68710365	GAAGGCAGAGTCTCC[C/T]AGAAGGATGTGGCAT	10391
rs537029127	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68576272	TTGTCTGAGTTTGCC[C/G]TTGCTTTTCTAGACC	10391
rs537050916	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68609500	CTCTGTCCCAGACTT[C/G]GGTGGAGAGGAAAAG	10391
rs537066815	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679989	TCCATGACTTCCATG[G/T]GGACAGTGATGGCCC	10391
rs537087673	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705758	CTAGGCAGAGCTGTC[A/G]CCTCAGCATGTCAGC	10391
rs537102097	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68705275	AAACCTTATCTCTAC[C/T]AAAAATACAAAAATT	10391
rs537105481	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569754	GTTGCATTCCTACCA[A/C]CAATGAATGAGAGTT	10391
rs537107395	snp	C/T	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68683444	GGTGCAAGCACTGTC[C/T]TTTTCTTTTGATTTT	10391
rs537131677	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618438	AGTGGCACTTGAGCT[C/G]AGTCCAGATGTGTGA	10391
rs537136774	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643703	GAACTTCTTCCTTCA[A/G]TAAAGAGGAGTTTGT	10391
rs537177858	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68634136	AGAAGCCGGAGGCCA[C/T]GAAGGAGGGGGTGAG	10391
rs537178361	in-del	-/AT	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68664692	AACCTGAGTGTTATC[-/AT]ATGTTTTAATTTTTT	10391
rs537205342	snp	A/T	0	0	intron-variant	CORO2B	GRCh38.p7	15:68610492	GGAACAACAGACCCC[A/T]TGCTCTTTCGCTCAC	10391
rs537209239	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68672954	GGGGGGTACCAGGGT[A/G]TGGGGTATGGGTTGA	10391
rs537215158	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68624242	TGGCACAAGACTTGC[A/T]GTGGTGTGAGACTGC	10391
rs537246415	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68602593	CCAGCTGTAACCTCC[-/A]CGGTTCCCAGGGCTC	10391
rs537248307	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630636	TTAGGCTGCGAGTAA[C/T]AAAGAAAGCCAACCA	10391
rs537269613	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679284	ACATATAACCCCAGA[A/C]TGGCAGAGCTGGAAG	10391
rs537288618	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68616959	AAGGAAGGAACTAAA[G/T]TTTACAAACACTAGG	10391
rs537297114	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709578	CCTCCCATCTCAGCC[C/T]CCCGAGTAGCTGGGA	10391
rs537299305	in-del	-/TGGATGGATGGATTGT	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68697131	TGGATTGTGGATGGA[-/TGGATGGATGGATTGT]TGGATGGATGGATTG	10391
rs537313115	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583801	GGGAGAGGAAGTAAG[A/T]GAGCCAGCACCTCAG	10391
rs537345018	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681671	GGGAACAGGGTGTGC[C/G]TGCCCCTCGAGGGCC	10391
rs537359524	in-del	-/AAAAG	0.0170251	0.090679	intron-variant	CORO2B	GRCh38.p7	15:68568019	TGAGAGTCCATCTCA[-/AAAAG]AAAAGAAAAGAAAAG	10391
rs537392216	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574480	CAAGCCCTCCTCACT[A/C]TGTAGAGTAGCACTC	10391
rs537400215	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667969	TAATAAATCCCACCT[A/G]GCAGGGTTGTCATGA	10391
rs537401008	in-del	-/TTTG	0.47575	0.107411	intron-variant	CORO2B	GRCh38.p7	15:68693829	TCTGGTTGTGATTTG[-/TTTG]TTTGTTTGTTTGTTT	10391
rs537408094	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68690446	GCCTACTGGCTCCCT[A/T]TTATGGAAAATGAGG	10391
rs537412858	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68659477	CAGCACATTGGGAGG[C/T]CCAGGCAGGAAGATC	10391
rs537413822	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68608224	CACAGGCATCCTTTG[G/T]GAAGAGCTAGGCAGG	10391
rs537448741	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626841	CTGGTCAGAGGCTGG[A/G]GCCCCAGCCCCCAGG	10391
rs537463170	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68674528	GTCTGCAAACCTGGG[A/T]GTGGCCTGGCACAGC	10391
rs537496396	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699860	CTACAAGGGAGGAAA[C/T]TGAGGCTCAGGGCCA	10391
rs537540324	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633441	AAAAGTTTCTGCTCT[A/G]GTTTCTAGACCCTCA	10391
rs537567154	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724920	GAGTCATTGGGGTGA[A/G]GATCTGCCAGGATAG	10391
rs537571283	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68701392	TCTCCGCTCACTGCA[A/C]GCTTCACCTCCCGGG	10391
rs537572134	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68708604	CCTGACCTCGTGATC[C/T]GCCCACCTCGGCCTC	10391
rs537580107	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632795	TGGGGTTTTGCCACG[C/T]TGGTCAGGCTGGTCT	10391
rs537591053	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68666369	CCCAGATTTAGGACA[C/T]AAGGTGGGTAGGGTG	10391
rs537610358	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68684969	AAGCAACCTAATCAG[A/C]TGGTCTGGAATGCAT	10391
rs537647814	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631895	TCGCAGTCAGTGTAA[A/T]TAGGCTGCTGGAATG	10391
rs537696913	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68638971	CAGTACTGGGTTCAG[A/G]GGTGTTGGTATTCTG	10391
rs537698299	snp	G/T			downstream-variant-500B	CORO2B	GRCh38.p7	15:68727993	GGGGCGAATAATTCT[G/T]TGCTGTGGGGGCTGC	10391
rs537716735	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693695	CCCCCTCCCAGGAAG[C/T]CATGGACTGAGCACC	10391
rs537721896	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722796	ATCATGGCTGGGCAC[A/G]GTGGCTCACGCCTAT	10391
rs537723801	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68701016	CGGGATGGACAGGAT[A/G]TCAGCCCTGCTGGAA	10391
rs537741822	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631263	TCTCCATGTATAGGG[C/T]ATTGTGAGGAAGACC	10391
rs537762343	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702849	TTTTTTTTTTTGAGA[C/T]AGAGTCTCACTTTGG	10391
rs537771721	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68605754	TTGAGATGGAGTCTC[A/G]CTGTGTCGCCCAGGC	10391
rs537782295	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678657	CCAGCCTGGGCAAAA[C/G]AGCGAGACTCCACTT	10391
rs537796308	in-del	-/C	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640145	GTCCTTCTGCAGACA[-/C]CCAGCTTTGGCCCAC	10391
rs537801071	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668659	CTGGGCTACCCAGAA[C/T]CTTGGAGACCACGCC	10391
rs537819677	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578578	CCGCCGCGCCACACT[C/T]ACGGCCCACGGGCCG	10391
rs537825309	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713060	TGCTGCCAACTTACC[C/T]GATGCCGAGGACTGT	10391
rs537841976	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68682139	CCCACCAGGACAGCC[A/C]ACAGAGGGAGAGTCC	10391
rs537849736	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68647162	AGAGGAAAATGGAGT[C/G]CATGTTTAAAATCAT	10391
rs537856458	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689217	GACTCCAAAGAATAG[G/T]TCTCTTCCTCCACCC	10391
rs537877978	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68642353	CCAGGGAGAGCCTGC[A/G]GTGACGTCTGCACTG	10391
rs537886427	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712776	TCCTCTCATGTGATA[C/T]GTGAGAACACTTAAC	10391
rs537894714	snp	A/C	0.000281725	0.0118652	intron-variant	CORO2B	GRCh38.p7	15:68719270	ACAGAGCACAGGCGG[A/C]TGCAGCCTTTGCCTT	10391
rs537942378	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558879	TCTGGCCTCAGTTCC[C/T]TCATCTCCAGGTCTT	10391
rs537949789	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68585438	ACTCTGTACAACCAT[A/G]GGGTAGATTCTATTA	10391
rs537957154	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654966	TTTGTGCCTAAAGGG[G/T]TACAGGGATGGTGGT	10391
rs537977126	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600290	TCCAGTGTCACCTCC[C/T]CCAGGAAGCCTTCCT	10391
rs537983001	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68675425	GCCTCTGAGGGCAGG[A/G]ATAGCATCTTCTAGG	10391
rs538035065	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68680411	AATAAAGCAAACAAC[A/G]CAAGACAATGCTAAA	10391
rs538036361	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694918	CCACCATGGCTGTGT[A/G]GCCTCCCTGAACCAT	10391
rs538047049	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68687100	GGAAGCATGGCACTC[A/T]GTGGTTGCAGGTGTG	10391
rs538050510	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68694255	CTAAGCTGTACAATA[A/G]TAAGTGCTGTCATAT	10391
rs538086330	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68586608	ATCCCTGCTTTACAG[A/G]TAAGGACACAGGCAC	10391
rs538098702	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701416	TCCCGGGTTCAGGCC[A/G]TTCTCCTGCCTCAGC	10391
rs538107079	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563637	AAAAGTGACACACCT[C/T]TAGCTAGACTGATTA	10391
rs538154953	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725703	AAATGCACCTGGGGA[A/G]AATAAATGTATCAAG	10391
rs538158048	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68621743	GCTCCTTGACAGTCA[C/T]GTGACATTGGGCAAG	10391
rs538196714	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68571223	CCCAGCCACCTGTTC[G/T]GTACTCAGTACTCAA	10391
rs538213338	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618571	ATGTGCCTGGCACAT[A/G]AGCAGTGCTCTTCCT	10391
rs538237890	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68594382	GGATGGGTAGGTGGA[A/G]GCGCTTTTGGTACAA	10391
rs538247112	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68599351	GGAGGGAGCGTGTCG[C/T]GCCACAGATCCCATT	10391
rs538252104	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68565801	TCTGGATAGAAATAA[A/T]ACCTGCTTGGGCTTT	10391
rs538269806	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680333	TGCTGGAAACCCTCC[A/T]TGATTATCTCATTTA	10391
rs538279262	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726105	GAGGACCCCCGCCTA[C/T]CACCTCGAGAACTGG	10391
rs538300048	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639845	CGCCTTGTGCTCATT[G/T]GTCCTAAAAGATTCA	10391
rs538347848	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724146	AGCGGAGGTTGCAGT[A/G]AGCCAAGATCGCGCC	10391
rs538353979	in-del	-/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68585199	GTGGGGACGGTCCCC[-/T]CTATTTAGGGACGGA	10391
rs538364836	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608129	TTTCCTGCTACCTAC[C/G]TCTGGGGCAAGGTTT	10391
rs538385291	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592297	CTTAGCACACATAAG[A/G]GAATTTTCTGAGTCA	10391
rs538415061	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701772	TACAGGCGTGAGCCA[C/T]TGCACCCGGCCTAGG	10391
rs538446891	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68620891	ATCCCCCAACAAAGG[A/G]TAGAAAGTCTGCTGG	10391
rs538481179	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614090	GTTAAAATGCGGATT[A/C]TTGGGTTCTCACACA	10391
rs538483859	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68571827	TTTACAAATATAACG[A/G]GCTGAAATGCAGCAA	10391
rs538517495	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613383	GGCATATTAAAATGG[C/T]TTATCAAATTAGGGT	10391
rs538548488	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647563	GCGTGGTGGCACATG[C/T]CTGTAATTCCGGCTG	10391
rs538548696	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652370	TATTCCAGAGAGCAG[A/G]CACTGTGCCCAGCAG	10391
rs538574473	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668405	AGGGCGCAAACAGTC[A/G]TTAAGATTACATCAG	10391
rs538577850	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68579436	CCGCTCGAGTCACTC[A/C]GGCCCCCAAGGACTG	10391
rs538579141	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68611807	GACAAGATCTTACTC[A/T]GTCACCCAGGCTGGT	10391
rs538580087	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680976	ACCAGCACTTTGGGA[A/G]GCTGAGGTAGGCAGA	10391
rs538607240	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68657395	GGTGGCATATGCTAG[G/T]AGTCCCAGATACTCG	10391
rs538648347	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694833	CAGCTTAACTTTAAA[C/T]ACTTTTACTTGATGC	10391
rs538659643	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724908	GGTTAAGCTAGAGAG[G/T]CATTGGGGTGAAGAT	10391
rs538716103	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68557506	AGAGCTGAGGTTCAG[C/G]GGCCAGTCTATCCAA	10391
rs538760555	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68682012	CCCAGTCCCAGCCCA[A/C]CCTGGGTAGGAGTCT	10391
rs538779608	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68605657	GACTGGAAAGTGAAG[A/G]GAGAATGGACAGGAC	10391
rs538789786	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68676841	CAGTGGCACCATCAC[A/G]ACTCACTGCAGTCTC	10391
rs538793430	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68563504	AAAAAAAAAAAGAAA[A/G]GAAAAGAAAAAGAAA	10391
rs538822603	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68572830	TCCCAGCTGGCTCTA[C/T]ACAAGGGACTGGGCT	10391
rs538830396	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571117	GATCTGGATGGTAAA[C/T]ATCTCTTTAAAGAGC	10391
rs538834830	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700768	CGGTTTCCAAGCCTC[A/G]TGCTCCCAGCCCTTC	10391
rs538835874	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693666	GCCCCTTGTTCCATC[A/C]GTTTGTGGACTCACC	10391
rs538835902	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693242	TGCAAAAGATCAAAC[G/T]ATCTGGAAATGAGCC	10391
rs538853331	in-del	-/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68593762	GTGAGTTTGCTCTGA[-/G]GTGGCGAAGTGGGTG	10391
rs538899421	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699805	GAAGGTCCCCTGACT[A/C]CCAGTCTGCACTCTC	10391
rs538927975	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671431	CTCAGTTTCCCATAT[C/T]AAAATCTGAGATGAT	10391
rs538965307	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717070	GCAGTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	10391
rs538965673	in-del	-/GTTC	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68602749	ACATCAGTGAAGGAG[-/GTTC]TGTGCAATGTGCAAC	10391
rs538980105	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569663	AACTCCAGGGAGAAC[A/G]ATTGCTGGATCATAT	10391
rs539017653	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68669018	GGGAGGCAGAGGTTG[C/T]GGTGAGCCAAGACCA	10391
rs539020047	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600123	ATGGATGATCCCACA[C/G]CCTTATTGTTGGCTG	10391
rs539045200	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68573614	GGAGCTGAGGCATGT[C/G]GTGGGGGACAGCGGC	10391
rs539056764	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68607215	CATCTGAGAATCATC[A/T]GGAAGTGCCTTCACA	10391
rs539085551	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701316	CTTTTTTTTCTTTTT[C/T]TTCTTTTTTTTGAGA	10391
rs539090596	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614705	AGCCCTCTGGGGAAG[C/T]GGCTTCCTTTCCGTT	10391
rs539094938	snp	G/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68622336	TGTGAGGGTTGGTTG[G/T]ACATTCCCTTGAGCG	10391
rs539104271	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701978	CCGGGCACGGTAGCT[C/T]ACGCCTGTAATCCCA	10391
rs539127645	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646867	CAGCTCTAACACATT[C/T]GGAAGGATCCTCAAA	10391
rs539164836	snp	A/G	0.000115857	0.00761018	missense	CORO2B	GRCh38.p7	15:68713932	CCTACTAGGAGGCCA[A/G]CTGCAAAAACCACAG	10391
rs539166253	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564153	TGTCGAATGTGTTGA[A/G]GGGGATAGCAAAATA	10391
rs539180884	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68608356	GAAAAGCCAGCAAGG[A/C]AAGTTCTCCCTCCCC	10391
rs539237175	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68579527	CGCCCGGCCCAACCC[C/T]GGGACTGCATTTTTA	10391
rs539242050	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68675982	AATGGAATAGAATAT[A/G]GAATAGAATAGAATA	10391
rs539273837	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68720029	CTTTTGGGGCAGCTC[A/G]GCTGGGCCTTGTCCA	10391
rs539288477	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68620336	ATGTTAGAAAGAGCC[A/T]ATTTAAAGAAAATTT	10391
rs539319379	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594330	AGACATGGAACAGAC[C/T]ATTTCCTCCCATTTC	10391
rs539347756	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68634153	AAGGAGGGGGTGAGG[A/T]GTAGGACCTGCTGTG	10391
rs539352950	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712090	TAGGATGAGCCTGAG[C/G]GAAATGGCTAGGGTG	10391
rs539353655	snp	C/G	0.00114852	0.0239361	intron-variant	CORO2B	GRCh38.p7	15:68725800	CTTGTCTCACCTGCT[C/G]TCTCCTGGGCCCTCC	10391
rs539354415	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68593461	GAGCTTCCATTCTCT[A/C]GCAGCCAGGTCTGGA	10391
rs539396332	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702444	GTTCGCCCCTCCTAC[A/C]TCCCTGGGTTTGGTG	10391
rs539405598	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662520	TATTGCACTAAACAC[A/G]ATGAAAAATACATCA	10391
rs539409574	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68670437	CTCCTGCCTCAGCCT[C/T]TCAAAGTGCTGGGAT	10391
rs539413052	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677984	AATCTCCTGCCTCTC[A/G]GAGGCCTGGTGGGGC	10391
rs539457589	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703261	GTTCAAATGATTCTC[C/T]TGCCTCAGCTTCCCG	10391
rs539510290	snp	C/G/T	0.00914312	0.0669923	intron-variant	CORO2B	GRCh38.p7	15:68589902	ACCATCAGGCTGCGG[C/G/T]TGCCCAGGCCTGGCA	10391
rs539522584	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68723413	AGGTGTGAGCCACGG[C/T]GCCCAGCCAATAGAT	10391
rs539524866	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68661868	AAAAATTAGCCAGGT[C/G]TGATGGCGTGCACCT	10391
rs539562544	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68580475	CAGGGCCTACCCTTG[A/C]CCTCCTGAGGTCTGC	10391
rs539563196	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642587	CCAGCAGGTCTCCCC[A/G]TGGCCTCCACGACTC	10391
rs539581475	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68580460	CTCCTTCTGGTAAGC[C/T]AGGGCCTACCCTTGC	10391
rs539589830	snp	A/G	0.00953873	0.0683987	intron-variant	CORO2B	GRCh38.p7	15:68669073	AGAAAGAGAGAAAGA[A/G]AGAGAGAGAGAGAGA	10391
rs539608271	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604239	GGGCTCCAGCATTGC[C/T]CAGAGTTTTTGGGAC	10391
rs539610048	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726717	GAACTGAGGGTTGCA[A/G]TGGGGAAATGACTTA	10391
rs539639853	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68602633	TGGCTGGTGGGAGCC[C/T]CCATAGCTCTGCCTG	10391
rs539643877	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68682982	CCTTGGGCCAAATGG[C/T]GAACAGAAGGAGGGG	10391
rs539649471	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576804	TGCAGGTTAAAGGTA[C/T]ATTTTGCTTGATTTG	10391
rs539675378	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642149	TCAAGCAATTCTCCT[C/G]CTTCAGCCTCCCGAC	10391
rs539708548	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726047	ACTTCTCCCTTACCA[C/G]TGACCCCAGAGACAG	10391
rs539721271	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68704250	TCTGAAAAAAAAAAA[-/G]GAAAACTATAACCCA	10391
rs539800120	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68582154	GCTGCTAAAGCTGCC[A/G]GCAAACCCTGTGGTT	10391
rs539806904	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653929	CCCTCCAAGGGAATT[C/G]AGAGAGCCTTTTCCA	10391
rs539918155	in-del	-/A	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68558566	TTTTTTGTAGAAATG[-/A]GATCTTACGTTGTTG	10391
rs539921794	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68636753	AGGTGTGGAGGTTTG[A/G]ATTGATTCTTTTCTT	10391
rs539922209	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727451	TGAGATCTGGAAATC[A/C]AGAAATGGGTGTCCA	10391
rs539937178	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68612679	GTCTGCTGATGATAA[C/G]TTGCTCTCTAACTGA	10391
rs539949019	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588315	CTGTTTTTACTCTGT[C/T]AGGCTAGTTTGGTGC	10391
rs539949111	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595798	TGCCTGGGAGGCAGA[C/T]GGGCAAACAAATACG	10391
rs539966137	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68706211	CCTGCTGGCGCCCGA[A/C]CCCACACACACTGGG	10391
rs539973278	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68683732	CTCCCTCCCTGCAGA[A/G]CATGTTCTACCTCTC	10391
rs539975951	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641410	CTTCCTGTGTCTACA[C/T]CCTGAGGACTGGGGA	10391
rs539988327	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68636837	GTCTTTTCTCCCAGT[A/G]CTGTCCAATGCAACA	10391
rs540001614	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68665299	TTTCTGAATGTATTT[A/G]GGTTTATTTTACAGA	10391
rs540026689	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68619861	CTTTTTGGGTGGACA[A/G]TGCTGGCATCGTCAC	10391
rs540034410	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595122	GCAAAGTCCCAACTC[G/T]GCAGCATTCGAGGCC	10391
rs540036493	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690946	TTACAGGTGTGAGCC[A/G]CTGTGCCTAGCCTAC	10391
rs540086736	snp	A/T			missense	CORO2B	GRCh38.p7	15:68719527	TAGATTTATTAGAAA[A/T]TGTCCCACCCAGGAC	10391
rs540114115	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68685228	TTCTTAATTTTGTTT[C/T]GGGAGACAGTCTTAC	10391
rs540127420	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718473	TCCAATTCTAAAGCA[C/T]GCACTGTGGTGAGGC	10391
rs540139804	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68687752	CAGGCATCTGGCAAC[A/G]GCCTTCCTGCTATGA	10391
rs540141677	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724483	ATGGTAAAATTCATC[A/C]TCTGTAGTGTGTCGG	10391
rs540144995	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68608869	ATTCCCTTCCACTGT[C/G]TTTGCTATTTCAGCC	10391
rs540150309	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68686521	AGTGTCTCATCCATA[A/G]AATGAACTGTTACCA	10391
rs540164851	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559167	AGCAGACCTGACTCA[C/G]TGGCGTCAGTGCTAC	10391
rs540180755	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565950	GAGAGCAGAAGGGAG[A/C]CTTGGGGTGTTAATT	10391
rs540182563	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68607818	TGAGACCCTATCTCA[-/A]AAAAAAAAAAAAAAA	10391
rs540186447	snp	A/C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669223	AAGCCGGAGACAGGA[A/C/T]TCGGCCTTGAGAAGC	10391
rs540191542	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68606628	GTGGAAGAGGCTGTG[C/T]AGAAAATACAGTTTG	10391
rs540221785	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694563	ACGCTCATTCATATC[A/G]TAGAGAGAATGGCTC	10391
rs540229329	snp	A/C/T	0.00159649	0.0282165	intron-variant	CORO2B	GRCh38.p7	15:68572396	TAACCTCCTTGTCTT[A/C/T]GGTGGAAAGATCTAA	10391
rs540237627	snp	C/T	0.0248432	0.108648	intron-variant	CORO2B	GRCh38.p7	15:68605965	TCCTGAACTTGTGAT[C/T]CGCCCACCTTGACCT	10391
rs540245140	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675964	GTATAATAATAGAAC[A/G]GAAATGGAATAGAAT	10391
rs540263475	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68580697	ATGCTATTCAGCTGG[A/G]AGGGATATTAAGGTT	10391
rs540280578	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700949	AAGCTCTTCCATCCT[A/G]TGTCTGCTCTCCTCA	10391
rs540292807	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700597	CAGGGGCTTTGGGCC[C/T]GAGGGAGGGCTGGGG	10391
rs540303434	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571258	CAGTACTCAGTACAT[A/G]TAAATACAGATGCAA	10391
rs540338154	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68570725	GGGAAGGAAAGGGTC[C/T]GTGTTCAAACAGTCA	10391
rs540344825	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68712797	AACACTTAACCTTAG[C/T]GAAGTTGGGAGACTC	10391
rs540355780	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68675339	CAATTCCCTTTCCTC[A/G]GTCAGTTCAGCCTCT	10391
rs540360491	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713488	TGAAAACAACAGAAA[C/T]GTATTCTCTCACCAT	10391
rs540370563	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635089	AGATGACCTGGGGCT[A/C]GCACTCCAAGGATCT	10391
rs540400307	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68682288	TCTTGCTCTGGAGTT[C/T]GAGAAGAGACCAGCA	10391
rs540440915	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674105	CTGCGTGTGTGTCTC[A/G]GGTCCTGGTCGGCTC	10391
rs540473522	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68570393	TCTTGTGATGTCTTC[A/G]TCTGAATTTGGTAAT	10391
rs540498622	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68710422	CAACATTTGCTAAAA[A/G]GGGCTCATGCATGTT	10391
rs540514606	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593017	AGCATTGCACCAGCA[C/T]CTGGTGAGGGTCATC	10391
rs540515771	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68647467	GGCCAAGGCAGGCAG[A/G]TCACCTGAGGTCGAG	10391
rs540526272	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647059	GGCTCACAAGGGTCA[A/G]CAAGCAATACCTCAC	10391
rs540531335	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68558372	ACTCCCTTCCCCCTC[A/C]CCATTTTTTTTTTAA	10391
rs540535029	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688181	CAATCAAGGCTATGG[A/G]AGGTGTGTTTTTTGT	10391
rs540548219	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68594559	TTTCTGAATAACCAG[C/G]AGCAGATCTAAAGCA	10391
rs540549621	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68607673	AAATTTAAAAATCAG[A/C]CAGGTGCAGTGATGC	10391
rs540559875	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640748	ATTGCCGTCCTTTGT[A/C]GGAAATGCATGCTGA	10391
rs540560240	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680516	TTGAGTTGTGCAGTG[C/T]ACAGTCCATGCAACT	10391
rs540579393	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595954	AGCGTGAGCAGAGGC[A/C]AGGGCAGCGACGCCG	10391
rs540591645	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68721246	CCTCACAGTCTTAAG[A/G]GGGAGATTGGCAGGT	10391
rs540600221	in-del	-/A	0.229429	0.249152	intron-variant	CORO2B	GRCh38.p7	15:68657518	ATGAGATCCTGTCTC[-/A]AAAAAAAAAAAAAAA	10391
rs540604690	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622073	GAGCCACTATTTGAC[C/T]TTCTGAGTCTTGGTT	10391
rs540643141	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627962	ACTTCTGTACCCGAA[A/G]TCTTCCCTCCCTGCC	10391
rs540654426	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68579869	AGGGAATGTGACAGG[C/G]GAAGCAAAGGTGGGC	10391
rs540657912	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595293	GCTAAGCCCTGCTGT[C/T]CTGTGTCCCTGAGAA	10391
rs540658900	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68683882	TATAACCATGGGCAT[A/G]GCATGGGCAGTAGAC	10391
rs540662795	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68715162	CTGGGACCAGGCCCT[C/G]CTCTGCCCTCCCTAC	10391
rs540700036	snp	A/G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68696111	AAAAACTAGGTGGGT[A/G/T]TGGTGGTGCACACCT	10391
rs540738750	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68671937	GGTTAAAGTGCTTAA[C/G]AGGGAAAGGTGTGTT	10391
rs540757303	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68634329	ACTCACTCGCTGGCC[A/G]GCAGGGTGGTTGTCA	10391
rs540785273	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601639	GGAAGAGGAGGATTT[G/T]GCCAAGAGAACAGCT	10391
rs540785620	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593665	TCTCTGGGTTTGTTT[G/T]TTTTTTTGCAACTCT	10391
rs540798094	snp	A/C	1.658e-05	0.00287919	missense	CORO2B	GRCh38.p7	15:68725903	AAAGAGGAGCTGGCC[A/C]AGAAGGACATCCGCA	10391
rs540847717	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641224	CATCCCCGGGGAACA[C/T]GCTGAGTGGGAGAAC	10391
rs540855939	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68689714	GCATATGTGGGACTT[C/G]GGGAGAAGATTGCTG	10391
rs540866744	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702702	CTGTGCTCTTGGACC[A/C]AGGCACCATCTCTGT	10391
rs540869493	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600512	CCTGTAGGACTTAGT[C/G]GGAAAGACAAAGCGG	10391
rs540877338	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702159	CAGGAGTGTGGAAGA[C/G]AGGAGGAGGGTAGTC	10391
rs540880264	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68718938	GTCTTCAAACCTAAT[C/T]TGGGGTGAGGGGCAT	10391
rs540895671	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565570	CTCAACAAAACATTT[C/T]CTCTGTCTGCATTTC	10391
rs540915574	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615819	AGCCATGAGAAATAA[A/G]TTTATGTTGTTCATA	10391
rs540921058	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617626	AGTAGGACCAGATAA[A/G]CTCTAGGTCTTTCCT	10391
rs540921329	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708387	TTTTTTTGAGATGGA[A/G]TCTTGCTCTGTCACC	10391
rs540926793	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68588465	AATAAAGCATCCAAA[C/G]CTTGATCTGTATTAT	10391
rs540936272	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68573164	TCACCCCTCAGAGGT[A/G]AAAGACAACACCCCA	10391
rs540948314	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662635	CACATGCATTTTAAG[C/G]AGATACTTGCAACAC	10391
rs540978142	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588575	GGGCAGAAAGACCAG[G/T]TTCCCACTGTCAAAT	10391
rs540987078	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68622632	AAGCAGCTCAGCCCT[A/G]TGGAGCACCTTCAGA	10391
rs540993440	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651378	CCTTCGTTGATCTGG[C/G]AGCGGTGGAGATGTT	10391
rs541025768	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68603930	TGGGGAAGAGTGCCA[C/T]GTTGTAGAATTCAGA	10391
rs541050314	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561353	GCAGCTCACTCTCCC[C/T]GGTCCAGATGGTCAC	10391
rs541096613	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690499	TCTCCCTTCTTACTA[C/T]GCACACATACACACT	10391
rs541114008	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617154	CTTTCCAACAACATT[A/G]GCTTTCGTGGGCTCC	10391
rs541118777	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68642238	ATGGAAGTGGCACAG[A/G]GAGGTTAAGTGATTT	10391
rs541121147	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597750	CAGAGAGGAACCTCG[A/G]GCAAAAGTCCAGCCT	10391
rs541132896	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68649539	CTCGTTCTCCAGCGT[C/T]CAGTCTCAGGATCAC	10391
rs541148246	in-del	-/A			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640513	AGGCAATGCTATTTA[-/A]AAAAAAAAAAAAGGT	10391
rs541150428	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68627590	CATAAGGAGCTCGTG[A/G]GAGAGGAGACTCTGC	10391
rs541179317	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68709880	ACAGGGCAGGGATGT[C/T]CCCCCCACCTACCAC	10391
rs541199778	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	CORO2B	GRCh38.p7	15:68616571	GGGTGCCGTGGGCCA[C/T]TGTGCAAGTCTTCCA	10391
rs541201642	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623843	AGCCCCAGCCCCTCC[A/G]TTGTCGACACCACGG	10391
rs541257297	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716537	CACATTCCACTGAGC[A/G]GGAGACAGGCAATAA	10391
rs541295062	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582478	TGCTTTCCCTGAGAC[A/G]AGTAGCTCCAGCTGA	10391
rs541298236	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655379	AGTCCTCACAGTCCA[C/T]GCCTCTCGCCGGCCC	10391
rs541304252	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614951	TCGGGTGGGGTGGGG[A/G]CTTGCTCCCCACAGA	10391
rs541315310	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68666293	GCAAATACTGAAAGT[A/G]AGGCCCCAGGCAGCT	10391
rs541319065	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68715923	AGCAATTCTATATTT[C/T]GGGTCCAAATCACCC	10391
rs541325448	snp	C/T	0.000280221	0.0118335	intron-variant	CORO2B	GRCh38.p7	15:68715168	CCAGGCCCTGCTCTG[C/T]CCTCCCTACCTGCCA	10391
rs541358190	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68662034	AATAAATAAATTAAT[A/T]AATTAATAAAAATCT	10391
rs541387371	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68662387	TGCAGGGTTTTCATG[C/T]CTGCTGGCATAACTC	10391
rs541396410	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726306	GCAAGAGGGGAAGCG[A/G]GATCCCAGCTAGACT	10391
rs541425551	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68617122	CAGAGCCAGGTCTGT[C/T]AGCCTTCAAGCCCGT	10391
rs541475509	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698582	CTGACTGACAGACCA[C/T]GGTATGCCTTGCACC	10391
rs541497076	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68610130	GTAGGCATTGAACGA[C/T]GCAGAGATCTCGGGG	10391
rs541500674	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608397	TCCCCTGGAGGACTT[C/T]GGCCTGAAGGACAAC	10391
rs541510028	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568346	TTAAGTGAGGTAATG[C/T]GTATAGAGTGCCTAA	10391
rs541527725	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703584	CCATGGTGAACTCCA[A/G]CTCCTCCTGTGAACT	10391
rs541528189	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703585	CATGGTGAACTCCAA[C/T]TCCTCCTGTGAACTT	10391
rs541536325	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600651	ATGACCATGGGTGCC[A/G]ACCAGTGGGCAGACA	10391
rs541546940	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68567505	TCCATTGCAACTCCC[A/G]ATTCTGTCTCTGCTG	10391
rs541555566	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656858	TGTTCTGAGGATTCA[A/G]TGAGGTGTTACATAA	10391
rs541586575	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68607931	GACCCCAGGGCCTTT[A/T]TCATCTTCTTGTCAA	10391
rs541591786	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671416	ACATGGCTTACCTGC[C/T]TCAGTTTCCCATATC	10391
rs541628197	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614778	GCGGGCCCTTTATCC[A/G]CTCCTCTCAGCTCTG	10391
rs541637839	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708944	CCTTGGCTTCCCAAA[A/G]TGCTAGGATTGCAGG	10391
rs541638390	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574698	CAGCCTTGTGATTTT[A/T]AAAAAGAGAAACAAC	10391
rs541643189	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68695312	CCCTCCCTGCTTCCT[G/T]TGGAGGCCTCTCTTC	10391
rs541722268	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68579662	TGGTGCTGAGCAGTG[A/G]GTGTGGGGATGGGCC	10391
rs541724688	snp	A/C	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68685035	GTGGCCCATGAAAAA[A/C]CATCTTTCATACTGA	10391
rs541745322	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629180	GCTCCACATTGGAAA[A/T]TCTGCAGTAGTTCTG	10391
rs541754239	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68604995	GGCACACACCTGTAA[A/T]CCCAGCTACTCAGGA	10391
rs541783938	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68641741	TTTTTATTTATTTTT[C/T]TGAGACAGAGTTCGG	10391
rs541785029	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68620954	CACTTGGGAGCACAG[C/T]GAGCGGTACAGGGCC	10391
rs541786058	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68664839	GAATTGTCTGTCCAT[A/G]TTCTTCACCTATTTT	10391
rs541837724	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68682418	ACCCATCAGAGGCCT[C/T]TGGGAATCCTCTCTG	10391
rs541844384	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68567258	AGAAAAGCACATAAA[C/T]TGTATTAGTTTTACA	10391
rs541851055	in-del	-/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68558883	GCCTCAGTTCCTTCA[-/T]CTCCAGGTCTTAGTA	10391
rs541880190	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68696124	GTGTGGTGGTGCACA[A/C]CTGTAGTCCCAGCTA	10391
rs541890523	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68684085	GATTGGAGAGAGAAC[C/T]GAAAAGAGCAGACAT	10391
rs541896531	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68648474	ACATGGTGAAACCCT[A/G]TCTCTACTAAAAATA	10391
rs541898322	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68656249	GTGGGAGGAAGAAGG[A/G]TTGGTCCCAGCATTC	10391
rs541899077	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559279	AAAAAATAATCAGCC[A/G]GTTAATTCCCCCGTC	10391
rs541964575	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68660651	GTTGGGATTACAGGT[A/G]TGAGCCACTGCACCC	10391
rs541986855	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558464	CCTCAGTGACCTCCC[A/G]TGATTAAGAAATCCT	10391
rs541993106	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655250	CCAGGTTGGTGGGAG[A/T]AAACGGTGCTGGAAT	10391
rs541999606	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68670486	CGCCCAGCCAGCAAA[A/C]ATATTTAGAATCATT	10391
rs542005465	snp	A/T	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68662018	TCTCAATAAATAAAT[A/T]AATAAATAAATTAAT	10391
rs542005629	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654733	GCCTGGCCCATAGTA[C/T]GTGCTAGTAAACGGG	10391
rs542013135	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68614306	TTTGTTCTATTTAAA[C/T]ATATTGCAAAAGGAA	10391
rs542070467	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572245	GAAGAGTGCAGGAAG[C/T]CCAGGATGGTCCCAG	10391
rs542099087	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621330	GAGAACAACGCAGTG[A/C]GTGCCAGCATGGAGA	10391
rs542126848	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726965	CGCTCTGTGCCCCTA[C/G]ATCCTTCAGGTCCCC	10391
rs542141775	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668652	TCAGGGGCTGGGCTA[C/T]CCAGAACCTTGGAGA	10391
rs542155223	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635290	TCCTCAAAATAGGTC[A/T]GGAGTCTGGCACAGA	10391
rs542214313	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575315	CTCTGGATGCCTCCT[A/G]CAGTGACCCTGAGAA	10391
rs542214318	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68583961	CCTTCTTCCAGATAT[C/T]CAGCATTCTCATGCT	10391
rs542225126	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68591301	AGAGGCAGGAAAGGC[A/C]TTCCAGGTTGAGCGG	10391
rs542232027	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68678783	CCATGTCCCCTGGGA[G/T]CCCCAAACTCAGGCA	10391
rs542250589	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583395	AGGCTGGAGGGGCTG[G/T]CACCTCGGTCCTGAC	10391
rs542255043	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68688062	GTATGAACAAATACA[C/T]TGATGTTGCACAAAA	10391
rs542281729	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566307	GGAGAGGAAACAGGC[C/T]CAGAGAGGCTAAGTA	10391
rs542303349	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68702905	AATCTTGGCTCACTG[A/C]AACCTCTGCTTCCTG	10391
rs542305381	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708879	AGAGGCGGAGTCTCA[C/T]TATGTTACCCAGTCT	10391
rs542307817	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68643903	TTAGCTGGGCGTGGT[C/G]GTGGGCCCCTGTAAT	10391
rs542317399	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574541	GAAGCACATTAGGCA[C/G]GGCAGAGCCTCACAC	10391
rs542335007	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622807	TGTTGACCTTAACTC[A/G]CAACACCCCTGTGAG	10391
rs542356251	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574008	TGAGATGGGAAGCCT[A/G]GGGGATGGGGGCAGG	10391
rs542367882	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68582444	TTCCTAGGGCAGCTC[A/G]GGGCGAGGGAGCCAA	10391
rs542368467	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708518	GGTGCCTGCCACTAC[A/G]CCTGGCTAATTTTTT	10391
rs542394774	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574053	GTTGGACTTCAACCT[A/G]AGGACACCAGGGAGC	10391
rs542396623	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637538	GATTCCAGGACCCAG[A/G]TCAGTTGATACCCAC	10391
rs542404076	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68684779	TGCAAGTGTTGAGGG[A/T]TGTGCAAATGTGAGT	10391
rs542428961	in-del	-/CT	0.00914312	0.0669923	intron-variant	CORO2B	GRCh38.p7	15:68670048	GGTGACAGAGCAAGA[-/CT]CTGTCTCAGAAAAAA	10391
rs542440478	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68581635	TTCTGCTGAGCCTTG[A/G]TGCAGCTTCAGTTCT	10391
rs542444298	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68618243	ATTTTTTTTAAATAC[-/T]GGTAGCAGCCTACCA	10391
rs542458580	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68676934	GCACCACCATGCCTG[A/G]CTAATTTTTTTTCTT	10391
rs542462159	in-del	-/A	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68714882	CTGGAGCGGGCTTTT[-/A]ACATTGGAATAAAGA	10391
rs542466310	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691824	TCCAGTGTATCGCCC[A/G]TGGGCTGCTGGCTAG	10391
rs542470456	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68683342	GTTGGTCCAGACCCC[A/G]CGTCCCCAGCACTCC	10391
rs542477152	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580859	GCGCGAGCTCATGCA[A/G]CCTTCCTTCCCTGGA	10391
rs542491424	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68689881	GCACTGCAAAGTGAT[A/G]TGCTGGGGTTGGCTT	10391
rs542503464	snp	A/C/G	0.0178098	0.0926698	intron-variant	CORO2B	GRCh38.p7	15:68709886	CAGGGATGTTCCCCC[A/C/G]ACCTACCACCTACCT	10391
rs542504625	snp	A/C	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68720932	CACTCTGTTGCCCAG[A/C]CTGGAGCTCAGTGGC	10391
rs542524875	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587834	GTTCCCACAGCCAGT[C/G]AGGGACTCAGCCTGC	10391
rs542567654	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598792	GGTTTGTACAGAAAC[A/G]CTGCCAAAAGAAAGT	10391
rs542579122	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68723655	GATGGGGTTTCACCA[C/T]CTTGGCCAGACTGAT	10391
rs542634269	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68676491	ACCGCTGCCTAAACC[C/T]GTCAAATGCCAGACA	10391
rs542657102	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68686311	AAAGTGCTGGGATTA[C/G]AGGAGTGAGCCACCA	10391
rs542657625	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631407	ACATTTTACAGATGA[A/G]AACACAAGCTCCAAA	10391
rs542659441	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624058	AAGGACTGGGGTGGC[A/G]GGTCCTGCTGTCTTG	10391
rs542660034	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615877	CAGAAGCCTGAAAGG[A/G]CTGAGACAAGAAAGA	10391
rs542672100	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625546	ATGGAATCATTGGGT[A/G]TGCAGCCTTTGAGCC	10391
rs542703453	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716875	AGACCATCGGAGAGG[C/G]GGGCAGGGGCTAAAT	10391
rs542728311	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68693402	TCCTCCTCCTTATTA[C/T]TCTGATGAGGAATCT	10391
rs542734443	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68675216	TGGAATGTTTGTACC[A/C]CGCTTCAGCATGCTC	10391
rs542742755	snp	C/T	0.000399281	0.0141238	synonymous-codon	CORO2B	GRCh38.p7	15:68645321	CATCGTCACCGAGAG[C/T]GCAGGGGGCGGCTCC	10391
rs542762879	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671515	TCTGTTGTTGCATAA[C/T]AAATTACCCCAAAAT	10391
rs542778646	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68604620	TATAAGTTGTGATTT[A/T]AAAAAAAAAACCTCC	10391
rs542797048	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699959	GGGTCCAACCTGGGT[A/G]CTGGGGGAAAGCACA	10391
rs542832228	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636860	ATGCAACACACTGCA[C/G]TGATGGAAATGCTCT	10391
rs542839073	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561979	GGCTGTAAGTGCCCT[A/G]TCCCCCCACTGGCCT	10391
rs542848722	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68596068	GTGGCTTGCGGGGAG[A/G]TGGGAGTTGTGCAGG	10391
rs542857283	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611407	TTTGTTTGTTTTTTT[C/T]CCCCTATGACTGTAT	10391
rs542895668	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643005	CTTTTGCCAGGTCCA[C/T]CAACCACCCATACTG	10391
rs542921664	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68712198	GCCATTTGGAAGTAA[A/G]AAATTACCATTTTTT	10391
rs542923201	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727868	TCACCATGGTACCTT[G/T]ATGGTCAGCTCCCCA	10391
rs542926649	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569226	CATGTATAATAACAT[G/T]CATCCACCATCACAG	10391
rs542941131	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617921	CCCTAGTAACATGCC[A/G]TTCTGGATTACTAGA	10391
rs542997804	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687293	TGTTCTTTCTGCCTC[A/G]CTAAGCTGATTCTCT	10391
rs543003418	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582650	GTACATTAATAGAGT[C/T]GTGTGTAAAGTACAA	10391
rs543011469	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589778	TGGGAGGAGGCACCT[A/G]GTTGGAGAGACTTGG	10391
rs543022168	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68674240	GATGCTGCCCTCTGG[C/G]TAGGCGAGGCTTTCC	10391
rs543023774	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684501	GTACATATGTGTGTG[C/T]GTGTTCACTTGCACA	10391
rs543047210	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678143	ACAGCACCCGTGCCA[C/T]TGGCTGCTGGCTGTT	10391
rs543062910	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68700119	CAAAGCACCTGAGGC[A/T]TCGGCCACCGAGGCC	10391
rs543085196	snp	A/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684057	GGAAAATTAGGCAAC[A/G/T]GTGTGTAAGGTGGAT	10391
rs543086265	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722389	ATCATCGTAGCAGTT[C/T]GGAAGCAGCCAGTTA	10391
rs543090235	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68681290	GAAGTGCACTAAATC[A/G]TCTCAGTGGGAGCAG	10391
rs543104433	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68691086	TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCG	10391
rs543110158	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644782	TCTCCCATGCTGAAC[C/T]GAGCACAGTTCCAGA	10391
rs543145678	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652590	CTATAACCCAGCCAT[C/T]CTCAGTCCCAGCTGT	10391
rs543155204	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68562585	GCAGTGGGAAATACA[C/T]ATACAAAAAAATTAC	10391
rs543161041	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68649047	GTCAAATTGCTTAAA[C/T]GTTTCTAAACGCTTC	10391
rs543169080	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68570312	AGTACTTGCATGTAA[A/T]CACAGCAGTTGTTTA	10391
rs543170396	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612007	AACTCCTGGGCTCAA[A/G]CCATCCACCCACCTC	10391
rs543174298	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68595982	CCGTGGGGTGCTCCC[A/G]AGCCACGAGGGTGCC	10391
rs543206186	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652077	CGGCACAGCCGGGCA[G/T]ACAGTATGGACCCCA	10391
rs543216873	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68568273	GCCCCCCACCCCACC[C/T]CCATCCCCACAACAA	10391
rs543221167	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68650566	GTAGTGAGCCGAAAT[C/T]GCGCAACTGCACTCC	10391
rs543230216	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560670	TCTCTAAGCACTGTC[C/T]TCCACATACAACCCA	10391
rs543258732	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690554	CAGCATAGCACAATT[C/G]TTGCTTAAGATATAA	10391
rs543269022	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560004	GCCTCAGACGGCAAT[A/G]CAGATCTGACCAAGT	10391
rs543294411	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697646	CCTATAGTGAAGATG[A/G]TCCATCAGGCTTCAG	10391
rs543301964	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68593057	AGGCATCACGTCATA[A/G]TGAGTGTGTGAGACA	10391
rs543317962	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568525	CTGGGACCCCAAAAG[C/T]CAAAGTGATTGACCT	10391
rs543334301	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617265	GAGGAGGAGACAGGT[A/G]CATCAGCCACTGTGG	10391
rs543335632	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656543	CCCATGTGTCAGATG[A/T]TTGATCCTGGCAGCA	10391
rs543371134	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68624608	TAAACATCAGACCCA[A/G]GAGTTCCTGGGGTCC	10391
rs543374750	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68651630	TGGCTCCAGATTTTT[-/G]TCTTGAGCAAACAGC	10391
rs543379656	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606016	GCAGTGAGCCACAGC[A/G]CCCGGCCGGCTCTTG	10391
rs543400558	snp	A/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68670985	AAAAATTCATGTGTG[A/G/T]AAGAATTCAGCTACT	10391
rs543413265	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68597633	CCCCCCCATCAAAAA[A/T]AAAAAAATAAATAAA	10391
rs543423371	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644618	GAGATTTCTGAGGGT[A/G]TACCTGTGGATTAGA	10391
rs543431407	snp	C/T	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68653028	CATCTCTTTTGGAAG[C/T]CGAGAGAGTAGATGT	10391
rs543437484	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68626137	CAAAAAGACTCACTC[C/T]TCAGCAATTTTTTAA	10391
rs543458075	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68581424	GGACTGCTTTGCTGT[C/G]TACAAGCCCGCTGGT	10391
rs543461004	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637396	CGGGTGGAGGGGGAA[C/G/T]AGATGATCAGCTCTC	10391
rs543499504	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68603375	TCTTAAAAAAACACA[A/C]TTGCTAATCATACTA	10391
rs543500452	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68604516	TGTGGTTTTTTTTTT[A/T]AAAGGCGACTTTATC	10391
rs543506824	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68699203	AGGAAGGGCAGCTGC[A/G]AAGGGCAGTTGGACC	10391
rs543516443	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727723	TTTTTTTTTTCCTTC[A/C]CCATTGACCTTTGTG	10391
rs543520646	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68712999	GTTCAGAGTGTGTGA[C/T]GCCAGCCTGAATATG	10391
rs543535117	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652062	TTGGGGAAGCTGAGA[C/T]GGCACAGCCGGGCAT	10391
rs543569680	in-del	-/AGTC			intron-variant	CORO2B	GRCh38.p7	15:68600509	GTACCTGTAGGACTT[-/AGTC]GGAAAGACAAAGCGG	10391
rs543575198	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68610760	CTGTTTCTGTGAGGC[A/G]GGTTTGGGAGGCCAA	10391
rs543581279	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617798	CTCAACTTGAAATCC[C/T]CAGTGGGTGGTTGTC	10391
rs543604484	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570201	TCTGCCACTTACTAG[C/T]TATGTGACTGCATGT	10391
rs543612200	snp	A/G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68617161	ACAACATTGGCTTTC[A/G/T]TGGGCTCCAGGGAAT	10391
rs543613514	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68642319	CCAGTCCGGTTCTTG[C/T]GACCCTTCCCCTTGT	10391
rs543637910	snp	A/G/T	0.00151413	0.0274731	missense	CORO2B	GRCh38.p7	15:68710864	AACATCCTGTTCAGC[A/G/T]CTGGCTACGACTACA	10391
rs543648817	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68602237	GACTGGCTTTATTCC[A/G]GGGAATGACACTAGG	10391
rs543656928	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697056	TCCAGCACAGGGCCT[C/G]GTACCTAATAAATGC	10391
rs543666908	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68710153	CTCTATCCAGGCTCT[G/T]CCCATCCTTTCAGCT	10391
rs543690632	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609941	CACATTGGCCAGCTA[G/T]CCCATCCCCAGGGGA	10391
rs543708777	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583285	AATAAAATTTTGGAG[C/T]GGGCAAATCACCCAA	10391
rs543718004	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702773	CTGTATACAGCTAAA[C/T]TGGAGGCTTCTCAAG	10391
rs543721457	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575268	CAATTCTGTATCTGA[G/T]CCACGGGTCTCTGGG	10391
rs543726379	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609429	GGCTGTGCAGGCTTT[A/G]GGGCAGGGCATCAGT	10391
rs543750363	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68623905	GGGTCGCACAGACTC[C/T]TTGACTGCTGTGTTG	10391
rs543768718	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68627176	TATTACTTATAAAAT[A/T]TCATTTTTACTTGTT	10391
rs543780507	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693284	AGGCAGGAAGTGGTG[A/G]GGAAGAGGTCACAGC	10391
rs543781910	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68683663	CCCATCACATTTAAG[G/T]CCTCGAATGCTGGGA	10391
rs543790121	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630742	GGTGGCTCCACAGTG[C/T]CATCAAGGACCCAGG	10391
rs543793916	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68671553	GGTAGTTCTGGTTCA[C/G]GGTCTCATTTGGTTG	10391
rs543843917	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700564	AGGGATCCAGCAGAA[C/T]ATACCCAGGCCCTTC	10391
rs543844837	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68658337	TGGTGCTCTCCAAAG[C/T]GACAGCTGGGTGAGC	10391
rs543861227	in-del	-/A	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68682191	GGATGCCCAACTGCC[-/A]AAAAATCCTGCAGAT	10391
rs543881616	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68692784	GATTACAGGTGCCCA[C/T]CACCATGCCTGGCTA	10391
rs543890302	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68687500	CTGCTGGGTGAGCCA[C/T]ACCCGTGGACTCACC	10391
rs543893376	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68561907	CCTGTGAGCATGACC[A/G]TGAGTGTGTGTTGTG	10391
rs543935896	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68666931	TTGCCAGAAACCTGC[C/T]GCATGCCCTTGGGTG	10391
rs543937506	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570005	GGCCTTGGGAAAGTT[C/T]TCACCTGCAGAGAGA	10391
rs543943355	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651445	TCAGATTATTTTAGC[C/T]CCAGTTTTCACCCCC	10391
rs543966002	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68618937	GAGAAAGGGAAGTGA[C/T]GTGATCAAAAATTTA	10391
rs543971400	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561393	CCTCCCCGACTCTCC[A/C]CTGCCCTCACCCCCA	10391
rs543972308	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68576960	CAGGGAGAGCCATTG[G/T]GCTGGAGTTGTCAGG	10391
rs543977976	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698702	GTTACTTGGCCTCTC[C/T]GAGCCTCGGTTTTGC	10391
rs543995230	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68665598	TAAATATCCATGATC[A/G]TAGTTTACTTTTTGT	10391
rs544003901	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625572	GAGCCTGCTTGTGCA[C/G]TCCGTTACAGGTTTT	10391
rs544034286	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574351	GCATCTCCCTCTTAG[A/G]GGCTCTACAGCTTTG	10391
rs544050162	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664692	AACCTGAGTGTTATC[A/G]TATGTTTTAATTTTT	10391
rs544055428	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631660	TCAACACGTGTAAAG[A/G]GAACCAACCAACCCT	10391
rs544098562	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574793	TCAGGCGACCATGGA[C/T]ACAGCGCCAGGAGAG	10391
rs544111393	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703803	TCCATAATCATGTAC[A/G]CGTTTTAAAGATGAA	10391
rs544170106	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570469	TGAAGTCGTAAGACA[C/T]CGAAGGAAACTTCCG	10391
rs544179522	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68723579	TTGCTTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	10391
rs544194543	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612631	AAAGAGCACTGAACT[A/G]GATGGGGCCAGGCAA	10391
rs544199294	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578853	CCCGGCGGCCGGCGA[C/T]CGAGCGGGAGGCTCG	10391
rs544200936	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68586912	TTTATTTTTCCAAAA[C/G]GAAACTTTGCTCTGG	10391
rs544206814	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68681550	TAATCACCATTTTCA[C/T]AGGACCTGAGACATC	10391
rs544215882	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68667653	ATAAGCCAGGTTTGC[A/G]CTGGGCCTCTCTATT	10391
rs544225029	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68586351	AATAGCAGGGGGCCT[A/G]ACCTAGTCAGAGGGA	10391
rs544232639	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612067	GGAGCCACTGCACCC[A/G]GCCTCAACTTTCTAC	10391
rs544259607	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577802	CTCTATTATTATTGC[C/T]CCAATCTAGACACTG	10391
rs544297630	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68674746	TGGAGTAAGAGTTTG[C/T]CCTGATCCCAACTAC	10391
rs544317993	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718318	GTTCATTTCAGAGGG[C/T]AATGGGCTCTGTGGC	10391
rs544318477	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712848	GAGCTAGGATTCAAA[C/T]CCAGAGCCCATGCCA	10391
rs544326312	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68673950	AATAAAAGAAGGGTT[A/G]ACTTTTTCGGTGGAC	10391
rs544444447	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68584187	CCAGGAGACCTCTTG[C/T]CTTGCCTGCATACTG	10391
rs544462931	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68598616	TCCTGCCCTGGAGCC[C/T]GCTTGGCCTTGAACG	10391
rs544464513	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679010	CTGACCTGGCCCTCC[A/G]AGCTGGTCAGGCAGA	10391
rs544475109	snp	C/G/T	0.00159649	0.0282165	intron-variant	CORO2B	GRCh38.p7	15:68611187	GAGTCTGGAGTAACA[C/G/T]GCTCCATGATTCTCT	10391
rs544484442	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68560849	AAGCCTGCACAACCC[A/G]AGGGGACCAGAGGAA	10391
rs544505459	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723163	GTCTTGCTCTGTCAC[A/C]CAGGCTGGGGTACAA	10391
rs544542502	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68590834	GCCAGTTTTGCCAGG[C/G]AAGTGAGTGTGGAGA	10391
rs544589158	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675246	CTGGAATTCCCCTTG[C/T]GGCAGCTGCCTCCCA	10391
rs544609944	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68694076	CCTGACGTCAGGTGA[C/T]CTGCCCGCCTTGGCC	10391
rs544627504	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68653442	GCTGACCTATGGCCA[A/C]ATCACAGAGGCAGGT	10391
rs544631720	snp	C/G	1.66504e-05	0.0028853	intron-variant	CORO2B	GRCh38.p7	15:68719385	TCCATGGGATCGTCA[C/G]TGAGAGCGTTTCCCT	10391
rs544694346	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68622245	GAGTGACTGCATGTG[-/A]AAATGGAGTGTGTGG	10391
rs544703316	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640698	TGAGGAATGGTCAGT[A/T]TTCTCAGATGCGATG	10391
rs544706924	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68712777	CCTCTCATGTGATAC[A/G]TGAGAACACTTAACC	10391
rs544713976	in-del	-/CT	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68602804	ACTAAGAAGCAATTC[-/CT]CTCTGTTTTCTAATA	10391
rs544716395	snp	C/T	4.9884e-05	0.00499395	intron-variant	CORO2B	GRCh38.p7	15:68725831	TTGGCCCCCTCTCTT[C/T]CTCCACCCCAGCTCC	10391
rs544726334	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725294	GAATTGTTTGAACCC[A/C]GGAGACAGAGGTTGC	10391
rs544731030	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68593294	AACATTTGGTTTAAT[A/G]TTCTGTTGTCACTGT	10391
rs544744238	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68599701	TTCCACCCAAGAGAG[G/T]CAGTGCCCTGGTGAC	10391
rs544745287	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576217	TTTCTCAGTATCTCC[C/T]ACATGCAGAGGCCGT	10391
rs544756172	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68619477	CCTGGGGCTTCTGTC[A/G]TGGTGCTGGTGCCAG	10391
rs544765399	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646981	GCAGGTCCCCAGGAA[C/T]ATGTGGGCTGGTTCT	10391
rs544778802	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588025	CTGTGAAAATGAAGT[C/T]AGTAGTCTATCTCTG	10391
rs544860751	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68606390	CATCAGCATTTATTC[C/T]AAGCTCCCTGGATAA	10391
rs544875575	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68678850	CCAGTGCTCAGATAG[A/G]GAAGAACTAGAGTAG	10391
rs544898467	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605949	CAGGCAGGTCTCAAA[C/T]TCCTGAACTTGTGAT	10391
rs544906456	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643902	ATTAGCTGGGCGTGG[G/T]GGTGGGCCCCTGTAA	10391
rs544908351	snp	G/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68651958	CAACCGCGAAGATGC[G/T]TTGCCTTTGTACAGC	10391
rs544908895	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68610826	GAAACAGAGCATCAG[C/T]GTGGAAATGAACCTT	10391
rs544950253	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671669	CAGGAGGCCTCACTT[C/T]CTTGCAGGCTGTTGG	10391
rs544965780	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718479	TCTAAAGCACGCACT[A/G]TGGTGAGGCAGGTCT	10391
rs544983580	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727281	TGCAGATGAGGAAAC[C/T]GAGAGAAGTGGCCCA	10391
rs544988974	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68644059	AAAAAGAAAAACCAA[A/C]AACAAAAAAAACCAA	10391
rs544998267	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592744	CTGTACAGTATGTAC[A/G]GAATGTACAGTATTC	10391
rs545030796	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625487	TGCCAGCATTCATCC[A/G]TGTTCCATCTGTAGA	10391
rs545034685	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68592253	CAACCTTTGTGTTCA[C/T]TGTCATACATGTGGT	10391
rs545056664	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68584955	AGCTGCTAAGGAGGC[A/T]CAAGTGGGGTGGGGG	10391
rs545080307	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711082	GGGGTCCACAGAGGC[C/T]GGAGGCATCTTTTCT	10391
rs545086546	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68681060	CTCTACAAAAATACA[A/G]AAATTAGCCGGGCAT	10391
rs545088357	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723542	TCACTGCAACCTCCA[C/G]CTCCCGGGTTCAAGC	10391
rs545117843	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598891	GGAGCTGGGGCAGCC[A/G]TGCTGTGAGTCTGTC	10391
rs545120572	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624692	TTTTTTTTTCTTTTC[C/T]TTTCTTTTTATTTTC	10391
rs545124785	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717449	TGGGGAGAAGGAAGA[C/T]GGGGAGAACAGTGTG	10391
rs545125392	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679643	GCCCTGGGAGGAAGG[A/C]ACTTGCTCAGTCAGT	10391
rs545154857	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68598372	AGGGGGTGGAGATAA[A/G]TGGGAAGTTCTGCTG	10391
rs545159688	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68652358	GGGCCTTATGAATAT[A/T]CCAGAGAGCAGGCAC	10391
rs545173331	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68693924	CACCGCAACCTCCGC[C/G]TCCTGGGTTCAAGCG	10391
rs545187891	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723030	GGATATTGCACCATT[G/T]CACTCCAGCCTGGGC	10391
rs545190382	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613872	CTTAGCTCCAGTGTC[C/T]AACTGCTGCTATTTT	10391
rs545217737	snp	G/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68623418	GCAGTGTCCATGCAT[G/T]TGGAAGCCTGACGTG	10391
rs545238236	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693554	GTAGCAGGAAAAAGA[A/C]CTGAGAGATGGAAGC	10391
rs545255407	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597534	ATCCCCATTGTGCCC[C/T]AGGGCCCATGCTGTT	10391
rs545262491	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684869	CAGGACTCTGGGGGA[C/G]AAGGACTACAATACC	10391
rs545267283	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562677	AATTATAAAATACTT[C/T]GAGACAATGAAAACA	10391
rs545309643	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604445	CATCACTGAGGATAG[C/G]CCTAAGAATGCCTTG	10391
rs545341545	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68596831	GGGAGAAATGGCCGC[A/G]CATCACGCAGAGCAC	10391
rs545346889	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68627312	TTTGGAGTTAGACCC[A/G]AACACAGGAAAAGCA	10391
rs545364675	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68612049	GTGCAGAGGCTATAG[G/T]CAGGAGCCACTGCAC	10391
rs545385186	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68681168	CAGTGAGCTGAGATC[A/G]TGCCATTGCACTCTA	10391
rs545391736	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68705351	GCTGAGGCAAGAAAA[A/T]CCCTTGAACCCAGGG	10391
rs545406725	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68700005	GCTGCAGCCTGGGAG[A/G]GGGTGGGGCGTAAAG	10391
rs545420720	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674286	CTTTGGGGTCTGAGA[A/G]CTCCCTGCTGGGGGC	10391
rs545448128	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640588	CCAAATGCAACACAT[G/T]AACCTAGGTTTCACT	10391
rs545487973	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68632551	CTGCTTTAACAGTCC[A/G]AACTCTCCCTGGATA	10391
rs545510356	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68561194	GCCTGAGGGTGCTCG[A/G]GAGATAAGGGGGAGG	10391
rs545511368	snp	C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640150	TCTGCAGACACCCAG[C/T]TTTGGCCCACAGTGT	10391
rs545534946	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68557937	CAGGTAATATATTAC[A/G]TCTGTCCAGTTAGAC	10391
rs545539701	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68665393	CTAAGACTTCATAAT[A/G]TGTTTTAATATCAAC	10391
rs545550570	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653273	CAGAGTTCCTGGACC[A/G]AAAAGGAAGCAGTAA	10391
rs545567484	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68606800	AGCTTCTGATGGCCC[C/T]AGATAGAGGATGAGT	10391
rs545589799	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68644552	TGTAGCCTTGGACAA[A/G]TCACTTAACCTCTCT	10391
rs545596245	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701020	ATGGACAGGATGTCA[A/G]CCCTGCTGGAAGCCA	10391
rs545600652	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68620851	GTCAGGCAGGGTTGG[A/G]CGGGGAGCCAGTTTC	10391
rs545623390	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68713245	AAAATGGGGATAATG[A/T]TTTCTTCCGATAGAT	10391
rs545634504	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68706121	GACGAGATATGACAC[A/G]CATGACCTCTGGCCT	10391
rs545661323	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68659649	TTATAAAAGTCTATC[C/G]TCGGCCAGACATGGT	10391
rs545673894	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68719868	TAAATTCCTGACTAA[A/C]AGGGGCAAGCCCGGC	10391
rs545692927	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718925	GCTGTGAACTGGGGT[C/G]TTCAAACCTAATTTG	10391
rs545700719	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586084	AACACATGGCAGTCT[G/T]TCATTTACTTGCTGT	10391
rs545710521	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706738	TTTTAGAGACAGGGT[C/T]TCACTCTGTCACCCA	10391
rs545753234	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647621	TTGAACCTGGGAGGC[A/G]GGGGTTGTGGTGAGC	10391
rs545760843	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68673423	CTTGGGAGGCTGAGG[C/T]AGGAGAATTGCTTGA	10391
rs545769730	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68629418	TATTCTCACAAACGT[A/G]CCCTGTGGACTGGAG	10391
rs545772574	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565702	CTAGGAGGGCCACTG[A/G]CTGGGAGAGGTATTT	10391
rs545799499	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688715	TGTAATTTATTTTGA[C/G]AATGTCCCCATTGCT	10391
rs545810777	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626500	ATTCAGACAGGTGTT[C/T]TCCCCTGGGCCCTTT	10391
rs545811469	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662273	TGATTTCACCTTTTC[C/T]GGAATCATATTAGAA	10391
rs545829957	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558404	ACAGGGTCTCGCTTT[A/G]TTAACCAGGCTGGAG	10391
rs545832938	snp	C/T	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68607869	ATTTTTCACTCCTTT[C/T]TAAGAGAGGTCAGAC	10391
rs545837114	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701548	TGGAGTGCAGTGGCG[C/T]GATCTCGACTCACTG	10391
rs545849141	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68700174	ATGGTCAACTTGCTG[C/T]TCACCAGACACGACA	10391
rs545856168	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68695027	AAACACAGGTGATTC[C/T]TCAAGGACCTTCCAG	10391
rs545867301	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654544	TACCCATTTTCCTTC[C/T]AGGGCCTGGAGCCTC	10391
rs545868721	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68564450	CTGGGACTACAGGAG[C/T]GTGCCACTACAACCG	10391
rs545886545	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68622657	TTCAGAGTCACAAGA[C/T]TCACCCCCACACCCC	10391
rs545900391	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68707129	CCACGCCCAGCTGCC[A/G]CCTAGGCTTCTTAAA	10391
rs545923995	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68682681	TATCCCTGCCCCCCA[A/G]AAATGCCTCACTTTT	10391
rs545930276	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669263	TGTTCACGCCCAGAC[C/T]ATGGCCTGTTCACTG	10391
rs545936464	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68585377	ATCACCATCATCATG[A/G]TAATAACAGTTATTA	10391
rs545943797	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68581443	AAGCCCGCTGGTAGT[A/C]GCTCTTCCAGTACCA	10391
rs545966822	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661320	TTCTTATGATTTCCT[A/G]ATCTAGAGGCTGAAT	10391
rs545979012	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660660	ACAGGTATGAGCCAC[G/T]GCACCCAGCCAAGAT	10391
rs545982705	snp	A/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68720883	TATACCACCAACTTA[A/T]GCTATCACTATTTTT	10391
rs546006493	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68635165	TTCAAAGGTTTTCCA[C/T]CTTCACTCCTCTCCC	10391
rs546006649	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68689361	GACAATTCTGTGAGC[C/T]GACCATCTGAACAGT	10391
rs546042008	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634722	ATGTTTTCACAAGCC[C/T]ACCGGGTAATTGTGA	10391
rs546045126	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68634511	TCTGATGGAGGAACT[A/G]GGAGGTAAAGGGACA	10391
rs546046862	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578786	GTCCGCAGGCCCGAA[A/G]GGGTTAAGGCCGCGG	10391
rs546075481	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68627034	CACTGCCAAGTGGGG[A/T]TCCTTAGCAAGGTAC	10391
rs546094527	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641254	CATGCCTGCTCACCC[C/T]GAGCCTGAGCGCTGT	10391
rs546110176	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68599468	TCTATTCTGTGCATG[C/T]GTCATAGCTTCAGCC	10391
rs546114158	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674673	CAGTGGCTTCTCCGT[A/G]GAGCACACGCGAAGA	10391
rs546153965	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646374	CCACCCTCCGCCAAA[C/T]CGCTCAGGGGGAGGA	10391
rs546174635	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680247	CTGAATATAGACTGG[C/T]ATTGTGTTTGAGACC	10391
rs546189688	snp	C/T	6.64871e-05	0.00576534	missense	CORO2B	GRCh38.p7	15:68725951	GAACTGAAAAACTTG[C/T]GCAACAGCCCCAAGA	10391
rs546227486	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615043	GCTGGGCTTCTCAAT[A/G]CTGCCTCTGAGAGGA	10391
rs546236063	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68591836	CAGAGGACCAGAAGT[G/T]TCCTTCTAGGAAAAC	10391
rs546273456	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622121	GGATAATCTCTTTTG[C/T]TTAGGAGTGAGAATT	10391
rs546311166	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707904	AGGAAAGAGCATTGG[A/G]GTATTCTGGGCCCCC	10391
rs546329851	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693640	GGAACAGCTCTTCCA[C/G]ACCCATCCACGCCCC	10391
rs546342960	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720327	ATTCATAAGTGTCTA[A/G]CACTCTTCCTGGCTC	10391
rs546345287	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68652318	GGGGAGCAATCAGCA[C/T]CCTGATTGCCTGGCA	10391
rs546377303	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68676173	GTGTGGGCAGATAAG[G/T]ATATCTGATTGGCTC	10391
rs546387962	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68682335	GAAGACTGGAGTGCC[C/T]CAGGAAGGCTATGGG	10391
rs546453203	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726240	CCTCAGCTGGGTGAA[A/G]ACTACAGACTCCCTG	10391
rs546454314	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68587233	CCCCCTAAGTGTCTG[C/T]AGTTTGGTGTCTGCT	10391
rs546473009	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562157	CAGTCTGGAAGAAGT[G/T]GGCTGGTGAGTCCCC	10391
rs546489197	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68611695	TTATGCCTATATAAT[A/C]GTTTATTTTATGAAC	10391
rs546491201	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689397	TACAGTCATGGAACA[C/T]TGAAAAATCTTGACT	10391
rs546498681	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68663778	GAAAATGGATATCCA[A/G]ATAGCCAATAGGCCT	10391
rs546543857	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593810	TGCAAAGGTCCCATT[G/T]TGGGGTGGGAAGGTC	10391
rs546551284	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687550	GGGAGGGCCCGGCCA[C/T]GGCTGCCTGAGTGCA	10391
rs546571516	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725232	AAATTATCCAGGCAT[A/G]GTGGCACATGCCTGT	10391
rs546617065	snp	A/C	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68701211	CAGCAGTATGGCTCC[A/C]TGGCTAAGCAGCCAG	10391
rs546624693	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694059	CAGGCTGGTCTCAAA[C/T]TCCTGACGTCAGGTG	10391
rs546650870	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68614353	ATAAAATTGTGCATC[A/G]CTTCTTTTACGAAGT	10391
rs546698596	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68611107	CTGAGCCACTGAGCA[C/T]GACTCGTGGGAACCA	10391
rs546709306	snp	A/G	0.00755907	0.0610114	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68579212	CCCCGGGCCGCCGCC[A/G]CCGCCCCCGCACGCC	10391
rs546710350	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68563401	AGGCTGAGAATTGAT[C/T]ACTTGAGCCTAGGAG	10391
rs546724278	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616523	CCCTTAAAAGCAGGC[A/T]GCTGCCCTGGATCCA	10391
rs546744793	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68712282	ATATCTGAGGTTTGC[C/T]TTCTACACAAGAAGG	10391
rs546747451	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578222	ACTCCACCAGTAGAG[A/C]GGCACTCAGTGGTAG	10391
rs546777775	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613141	CTTTAGTCTTACATC[C/T]AGCTTACACCCAGTT	10391
rs546779816	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706452	CAACACCACACCCCA[C/T]TGGCTCATAGGAGGC	10391
rs546780269	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674795	CTCCAGCCTTTCCAC[C/T]AGTGCCCTCATGCTC	10391
rs546783489	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618999	GAAGATGGGCTCAAG[A/G]AGAGGCAAGGATACT	10391
rs546787110	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68666998	GATCTGTGGCTCAGC[C/T]GCAGCACAGGTGAGG	10391
rs546788855	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605028	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	10391
rs546811437	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570116	ACCATTTCTCTTGCC[A/G]TATGTAGATGACTAG	10391
rs546834692	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586610	CCCTGCTTTACAGAT[A/G]AGGACACAGGCACAG	10391
rs546840516	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68719990	TGAAGGTGCTCTCTG[A/T]ACCACTTGGAATGGG	10391
rs546841217	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712652	CTTAGCATGATTAGT[A/G]TTAACTGACATCTGC	10391
rs546841634	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68663445	TGGATAGTTGAAGAG[A/G]TACGTGCTTTCTTCC	10391
rs546853767	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68680909	CTGTGGGAAGAAGGG[C/T]TTAGAAAAGCTTAGG	10391
rs546869379	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667885	CGGGACCTGTAGTCC[C/T]GACCCAGCCATTTGC	10391
rs546932893	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68705673	GACTTGAATCCAGTT[A/G]AGGGGCTGGTGCCTG	10391
rs546942825	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68607133	GGGCCAGGCACAGAG[A/G]GGATAGTTTGTCTCT	10391
rs546957841	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68714375	TGTAAGACCCTTTCC[A/G]CTGCCCCTGGCTGCT	10391
rs546966154	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693989	TACAGGCGTGTGTCA[C/T]CATGCCTGCTTAATT	10391
rs546970603	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654171	TTTTGGAAGAATGGC[G/T]GCTGATTTTTGAGGA	10391
rs546983769	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613838	TAGTAAGAACACTTT[G/T]TTCTCATTGTCATCT	10391
rs547024908	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68632624	GAGACAGAGTCTTGC[C/T]CTGTCATCCAGGCTG	10391
rs547033981	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68676325	TCATGATGAGCTGCA[C/G]AAACCCTCCAGAGGA	10391
rs547098812	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668193	CCATGCCTGACACAC[A/G]GTGAGCCTCGGTCAG	10391
rs547108894	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587910	ACCCGGAAATATGTG[G/T]TCCAGAGCATGGGAC	10391
rs547110282	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68594743	GAAGTGAGACAGAGC[C/T]TGTGTGCTTGCAGAA	10391
rs547135479	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635363	TGTTTTGAGCTCCAC[C/T]GCCCCTCTCTGCCTG	10391
rs547150672	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627160	AAGCTGCTTCTAAAC[A/G]TATTACTTATAAAAT	10391
rs547152521	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68620057	GCTGGGATTACAGGC[A/G]CACGCCACAACACCT	10391
rs547155966	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713775	ATCCTTAGCTTAACC[A/G]CATCTGCAAGGACCC	10391
rs547215578	in-del	-/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68611525	TTGTAATATTTCAAA[-/T]TTTTTTTTATCTCTG	10391
rs547236761	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68600772	AAACAGTAAATGGGA[C/T]AGCCCTGGCCCAGCC	10391
rs547238595	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626714	CCCCATCATCAAGTC[A/C]ATTTCGTTGGCTGGG	10391
rs547240878	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68695394	TTCCAGCAAGCCCCA[C/T]GATGTGGGGGGGATG	10391
rs547295591	snp	G/T	3.90244e-05	0.00441709	intron-variant	CORO2B	GRCh38.p7	15:68718649	TGGGGTGATGTCACT[G/T]AGACGCAGTTTCTGG	10391
rs547307195	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68559523	GGGTGGTGAGGGGGT[A/T]GCGGGGAGGGCGAAG	10391
rs547336421	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688403	CTCCAAAATCTGAAA[C/T]TTCTTGATCACCAAC	10391
rs547344905	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68558672	TGAGCCACCGCACTG[A/G]CCTCTCTCCCCCTTG	10391
rs547346914	snp	C/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68672364	CCTCAGCCTCCCAAA[C/G]TGCTGGGATTACAGG	10391
rs547355424	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640974	GTGTGAAGACTTAGC[A/G]TAGGTTCACGTGGAG	10391
rs547359408	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68607944	TTATCATCTTCTTGT[A/C]AAAATCACATGCCCT	10391
rs547360054	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724861	CGTTTTGTGGACATC[G/T]GTCAATATGCTTTAC	10391
rs547408927	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572739	CTGATTAGGTGTTAT[C/T]AAAATTTAGATCCTA	10391
rs547413010	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669411	ATCTTGCTGGCCAGG[G/T]CCAAGGTGGGAAGTG	10391
rs547427079	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668952	GCGTGGTGGCATGTG[C/T]CTGTAATCCCAACTA	10391
rs547489379	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68587414	TCATGCTAATTGCTG[A/G]GAAGCCTCCATGATC	10391
rs547515956	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68634757	CCTGCAAGTTTGAGA[A/C]GCACTGAGCTGGAGA	10391
rs547527453	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650212	CGTCTCTACTAAAAA[C/T]ACAAAATTAGCGGGG	10391
rs547535802	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641319	CTAGCTGGGCTGTGG[A/G]GGCAACAGGAGATGG	10391
rs547557069	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68682040	TCTGATTGGCCAAAC[C/T]CAGTCCCATGCCCCG	10391
rs547580523	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68585838	GGGGGAGGAGGGTGT[C/G]CTATACATGGTGTTT	10391
rs547596412	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616120	ACTGGTTAAGTAATT[A/G]CCCAAGGACTGACTC	10391
rs547617912	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68688994	CCAATAACTCTGTCT[A/G]TTGGCATTGGCACAC	10391
rs547644795	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609649	TCCACTGCCAGGCCT[C/G]AGCCCGCTGTCCCCT	10391
rs547652797	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68620816	GGGCTAGAAGGTTTC[C/T]AGGCCTTCCCACTGT	10391
rs547677930	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558133	GAGTCAGTGAGCTGG[A/G]CCAGCCTGGCGGAGG	10391
rs547691989	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68653235	TCTAACAGATGGGTA[C/T]TGAATGCCTGCTAGG	10391
rs547693254	snp	C/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68647900	CGAGCATGATGGCTT[C/G]CCCTGAAGTCCCAGC	10391
rs547701409	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703027	AGACGGGGTTTCACC[A/G]TGTTGGCCAGGCTGG	10391
rs547751281	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636396	TGGTATAGAATAGAC[C/T]GTGTCTCTGGCTGGG	10391
rs547756386	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647255	GTTAGAATAAATTTT[C/T]AAAAGACAGTTTCTG	10391
rs547757079	snp	G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68677385	CCCAGACAGGGATAG[G/T]GCTAGCTGAAGGCCA	10391
rs547758841	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68634636	GCATCACCTGGCAAC[C/G]TGTTAGGGATGCAGA	10391
rs547792760	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623848	CAGCCCCTCCATTGT[C/G/T]GACACCACGGATTAC	10391
rs547813584	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68603320	GGGAGGGTATGCACA[A/G]ATGAGCGAAAGTTGG	10391
rs547844495	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633983	AACACGGGATCCCGG[C/T]TATCCTGAGAGTCGG	10391
rs547853807	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68598408	GCTTCTCTATTTTGC[A/G]TGGTCAGTGATTTTT	10391
rs547858251	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68595693	TACAAAATACCATCA[A/G]TTAAGCACCTGCTCC	10391
rs547864546	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697929	AGAAGGAATGCGGTG[A/C]CCACAGCTGGCTCCG	10391
rs547916556	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593872	AGCCATCCTGACCTG[A/G]GAAGGGCGAGAGAAG	10391
rs547987167	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68606889	CAGGGCAGGCACTTC[A/G]TAGGTGCTCAATATA	10391
rs547991028	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68698382	CAGGTCTCAATTTCT[C/T]CTGCCTGGCTCATGG	10391
rs548006042	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566546	TGCCTGCTGGGAGTC[A/T]GGATACCCGGCGGAC	10391
rs548008896	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68632793	GATGGGGTTTTGCCA[C/T]GTTGGTCAGGCTGGT	10391
rs548038852	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68696501	TTGCAGTGAGCTGAG[A/G]TCGTGCCACTGCAGT	10391
rs548049986	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68717672	TCACCTGAGGCAGGT[A/C]TTATCTGCTAAGTAG	10391
rs548061283	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702390	CCTCCCAGGACTCAC[A/T]GCAGTAGATGCTCAA	10391
rs548075367	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708188	CCCAGTCAACAGCCA[C/T]AGGAGCTGGCTCTGT	10391
rs548076499	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565834	TGGAGCACCTCAGCC[A/T]TTGCTGATGGTTCCC	10391
rs548103618	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662394	TTTTCATGCCTGCTG[G/T]CATAACTCAGGAATA	10391
rs548114954	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68573541	GGGCATCCCTGAGGA[A/T]GTGTGGGGAGGTGCA	10391
rs548137276	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669854	TTGAGGTCAGGACTT[C/T]GAGACCAGCCTGGCC	10391
rs548142281	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68649989	CTCCAGAGGTCCCCA[A/G]ACCATACACTGAGGA	10391
rs548161420	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675533	AGCTTTGCCACTTAG[C/T]TGCTGCGTGATCTTG	10391
rs548164514	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646712	ATCAGAAATCCTCCT[C/T]TGCCTACATCTGTCA	10391
rs548195603	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68700296	AGGGGCCCAGAGGGA[A/G]GCTCTTCACAGCAGG	10391
rs548210178	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700655	AATCCAGTTCTTTCC[G/T]CTGCTGGGTGATGTC	10391
rs548222927	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68660829	ATTGCCTCAGGCTTG[A/G]TGGCTTTCACAGCTT	10391
rs548274348	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681407	CAGTGAGGAGCCCCC[A/T]GATTTGGGGGCCATA	10391
rs548288114	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68658440	GGTTGTGGTTGGGGC[C/G]TAGGCCAGATAACAA	10391
rs548315784	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655553	CATGACATGCCTGGA[C/T]ACCCTCTGGCCCCCT	10391
rs548325405	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68655038	GCTGGGTGCCTGGAG[A/T]TGGGGGATTCTAGGG	10391
rs548326986	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647204	AGGCTTCCTAAGAAA[A/G]CCAGGAATCCCCCAA	10391
rs548329176	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600003	CCTGCTGCTTGGGGT[A/G]GGCCCCCTCCAGAGG	10391
rs548402807	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565763	CATGCTCACGCCTCT[C/T]ATTCCTTTCTGGAGC	10391
rs548436603	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699184	GTCAGTGAGAGGAGC[A/G]GGCAGGAAGGGCAGC	10391
rs548437773	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707900	GTTGAGGAAAGAGCA[C/T]TGGGGTATTCTGGGC	10391
rs548446032	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662358	TTCACAATGAGATAA[A/G]GTATTTTGAAAAGTG	10391
rs548476702	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68557318	CTGGTGCCAATCTAT[C/T]CAAGGTCATAGCAGA	10391
rs548480863	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654110	TCGCAACTTTATTTC[A/G]TTTGTCTGAGGCTCG	10391
rs548494631	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68573361	CAGAGAGATGAGAAG[G/T]GCAGGAGGGTGGAAA	10391
rs548515094	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669345	GTGTGAAATCCACAC[A/G]GGCATCTTGGCACCT	10391
rs548527156	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642088	GTTGCCCAAGCTGGA[A/G]TGCAGTGGCGCGATC	10391
rs548542865	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660790	TGCACAACATCTGGA[C/T]ACCGTTTTCTCCAGT	10391
rs548556896	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726552	CCTTCCCACCCTCTT[C/G]TCTTCAGGGAATTCA	10391
rs548562050	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647034	CGGCACCCTGCCATG[C/T]TCCACTTTAGGCTCA	10391
rs548570874	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68602543	TGCTGTGTCTTTAAC[C/T]GCCTCTCCCTATCGT	10391
rs548593493	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68605914	ATTTTTAGTAGAGAC[A/G]GGGGTTTCACCATGT	10391
rs548604251	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68708564	GAGATGGGTTTCTCC[A/G]TGTTAGCCAGGATGG	10391
rs548607705	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601830	CTGTAATAAAACACC[G/T]GAGCCATTTATAAAG	10391
rs548629020	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578490	TCCGTCTGGCCACCC[C/T]GTGCCCCGGGCCAGC	10391
rs548639529	snp	A/C	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68648877	TAATATTTAAAGATG[A/C]ATGTCTACTGACCTA	10391
rs548680571	in-del	-/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68707912	GCATTGGGGTATTCT[-/G]GGCCCCCTATACATC	10391
rs548689652	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68574303	ATGCCGCCTGGGGTG[C/G]CATAAGCGAGGCAGG	10391
rs548691623	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582710	TAAAGTCTAGGCCCT[G/T]GCAACCCGCTTTGTA	10391
rs548700979	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68567877	ATATAAAAATTAGTC[A/G]GGTTTGGTGGCAGGC	10391
rs548715758	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664265	TGTGCTTCTGAAATG[C/T]TGACAAAATTGCTTT	10391
rs548722789	snp	A/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702339	TTTCATGCATCCAGC[A/G/T]CCACAACGACCACTT	10391
rs548756612	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677898	CCCTGGTTCAGCCAG[C/T]CACAGGCTCTCTGCA	10391
rs548779137	snp	A/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614604	CTTTAGAGGGTCATG[A/T]GAGGAAAGCCCCGGA	10391
rs548787042	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68667286	ACAGCTCAGGGCACC[A/G]CCTCCAGGAAGCCAC	10391
rs548796294	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68586263	CATGTAGTGTTAGCT[G/T]TTATTCTCAGGAAGA	10391
rs548799412	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572668	CCATAATTTGCATTT[C/T]AAAAAAGCTCCCAGG	10391
rs548831994	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68724599	TTCCACACCCAATTC[A/G]GCCACAGTTTTTTTA	10391
rs548835785	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708080	AGTTTTTCGCAAGTG[A/G]GCTTTTGAAATGGAT	10391
rs548873344	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713690	TCTGTAATCTTACCT[C/G]TCTCCCACAAGGACA	10391
rs548880533	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68638750	TCTTTTAACTCCTCC[A/G]TGAGCCACACAGACA	10391
rs548896639	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68707519	GATTATATTCATCAT[C/G]GAACGGTCATACAAC	10391
rs548947259	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588829	ACAAAGGGATTTAAT[G/T]CCTGAGGATTTTTAT	10391
rs548950061	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68657143	GATAGATCCTTTTGG[C/T]AGTCTAGAAAAACCC	10391
rs548952274	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68603494	TTTAGGGCAGAGTTA[A/G]GGTGACATGGTGCTG	10391
rs548964044	in-del	-/GACAG	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68560167	ATATTGAATGTGAAA[-/GACAG]GAGGTGCTGGAGGCT	10391
rs548967987	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636296	TCTTGAAGAGAATGA[A/G]GCAGAGGTGGCTACA	10391
rs548989364	snp	A/C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631754	AGGGTAGGTCCCTGG[A/C/G]GATGGGATGGTCAGA	10391
rs549026008	snp	A/C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631062	GTGGTGGTGCAGGGC[A/C/G]GTTGGGGGTAGGGGG	10391
rs549044450	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723214	GCAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC	10391
rs549051845	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623459	AGTCTGGCCCACCCA[C/T]AGCTGTGTTTACACC	10391
rs549063421	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68592258	TTTGTGTTCATTGTC[A/G]TACATGTGGTGTAAA	10391
rs549065788	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708652	CAGGCGTGAGCCACC[A/G]TGCCTGGCCCTGCCT	10391
rs549068549	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68636471	AGACTGTTGAGAAGG[C/T]GCCATCCCAGCCCTG	10391
rs549075414	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717532	TGGAGGGGTGGAGAG[A/G]AAAGAAGCAGGAAGG	10391
rs549109798	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722608	AAAGTGGACCAAAAA[A/T]CAATGCAAAGAAATT	10391
rs549122828	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68602212	TGAAGTGGGAGTGGG[A/G]GGAACTGCTGACTGG	10391
rs549153399	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68583704	GCCTCCAGTTCCCTG[A/G]CGCAGAATCTAGGTA	10391
rs549164075	in-del	-/G	0.021333	0.101051	intron-variant	CORO2B	GRCh38.p7	15:68673834	GAGCGAGACTCCGTC[-/G]TAAAAAAAAAAAAAA	10391
rs549166382	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721838	CTATAACCTCAATCT[C/T]CGAGGCTCAAGCAAT	10391
rs549169071	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604194	CAGTATTGTCACTCT[A/G]GGCACCCCCTTCCCT	10391
rs549228290	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698738	TCTGAAACAGTAAGA[C/T]ACCTCCCTTTGGCTG	10391
rs549240659	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68582467	GGAGCCAAGGCTGCT[C/T]TCCCTGAGACGAGTA	10391
rs549257162	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603611	GGGTAAATGAGGTCA[C/T]AAAGGCAGAGCCCTG	10391
rs549259325	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637945	AATCATTTTTGAGAT[C/T]CGAGGACAGGATACA	10391
rs549275672	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644071	CAACAACAAAAAAAA[A/C]CAACTACAAAGTATA	10391
rs549278425	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609063	ATGCTGAGGCCAGGG[C/T]CCCCGGGTGCCTGCA	10391
rs549289468	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704190	GGCTGCAGTGAGCCA[A/G]GATTGCACCACTGCA	10391
rs549317250	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68584359	TGCCACCTTGACACC[C/T]ATGGCAGTTCTTAGA	10391
rs549340441	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727269	TCTACTCCCTTCTGC[A/G]GATGAGGAAACCGAG	10391
rs549352764	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68623243	CTTAGGGTCACACAG[C/T]GAGGAACCGGCCCGG	10391
rs549354655	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575710	ACCTCCACTGCCCCA[A/G]TCTTCCACTCCTGTG	10391
rs549391555	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68581829	TGAGCTCCCAGGGCA[G/T]TGTCTAGGGCTCTAG	10391
rs549397560	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708628	CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT	10391
rs549414297	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68641972	GGGTTCAAGCGATCT[A/G]TCCGCCTCAGCCTCC	10391
rs549421702	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68685736	TCCTGCCTCTCAGAT[A/T]TTGGGATTAAATTGA	10391
rs549423242	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68561083	ATGTTCCCTCCACCC[C/T]GCGTCCCCCAGGCTC	10391
rs549464764	snp	C/T	8.24178e-05	0.00641889	intron-variant	CORO2B	GRCh38.p7	15:68715209	CTCCATCTCTCCTGA[C/T]CCCAGGGTGATGGAA	10391
rs549472991	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68714505	TTCCTGGGATTTGGG[G/T]AGGGGTATGCCATCC	10391
rs549476099	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68645842	TCAATGGCGCGATCT[C/T]GGCTCACTGCAACCT	10391
rs549489479	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68588712	AGCAAATCATTTAAA[C/T]ACCTTGAGTTTGATT	10391
rs549491882	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68642899	GTGACCAAGCTCAAC[A/G]CCTCCTTTCTCGTCT	10391
rs549500102	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574289	GCCAGCATGTGGGCA[G/T]GCCGCCTGGGGTGGC	10391
rs549512923	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68620356	AAAGAAAATTTTTAA[A/G]TAAACATGGTTCGGG	10391
rs549529094	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622926	CTTAGCACGTGTCTG[A/G]TGCTTTGTATACTTT	10391
rs549546683	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68683312	GATACTGAAGACCCC[A/G]GAGCTGACTCTCTTG	10391
rs549573188	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68575724	AATCTTCCACTCCTG[C/T]GATCACCTTCCAATT	10391
rs549582172	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68677098	TTTTTGCAGCACTTT[C/T]GGGACTGTGCTCCCC	10391
rs549622848	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721354	ATGGGATTTGCTTTA[A/C]AATAACCCCTGAGGA	10391
rs549626014	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68561480	TTCCAGCTAACTGGG[A/G]CCCAGCGGGACAGGT	10391
rs549630045	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68643427	ATCCAGTGCTCCTGC[C/G]TCTCCAGCATGACTT	10391
rs549640775	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594351	CTCCCATTTCTAGGA[A/G]CAGCAAGCTGTGGGT	10391
rs549674375	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68651563	ATCATCACTTGGAGC[A/G]TTAGTTATAAGCTAT	10391
rs549708062	snp	C/G	0.00874735	0.0655527	intron-variant	CORO2B	GRCh38.p7	15:68559553	GTTGACCGTGCCAAG[C/G]CGGCCCGCTGGAAGA	10391
rs549737229	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650938	TGGTCAGATGAATGT[C/T]TTCATCTGCCTTGAA	10391
rs549741042	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630345	TTTTCCGGCAACTGC[A/C]TGGCAGGCACGGGCA	10391
rs549753398	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68720670	TGGACTCCTCCATAA[A/G]GCAGCTCACAACAGG	10391
rs549791409	snp	G/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68669996	TAGGAGACAGAGGTT[G/T]CAGTGAGCCAAGATC	10391
rs549795188	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68563992	AAATAGAAGATGAGG[C/G]AGCTTCCTGGCTCAT	10391
rs549800511	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68700370	GCCCTCCACTTCCCT[C/G]TACTTGTCTCAAAAC	10391
rs549803797	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622350	GTACATTCCCTTGAG[C/T]GTGAGCTGACTGGGG	10391
rs549822829	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68681492	TCTGTCAGAGAAGAA[A/G]TCTGGGAAAAGGTGG	10391
rs549825703	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68696278	AAGAGTTCGAGCATG[G/T]TGGCACATGCCTGTA	10391
rs549871956	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669484	TGTGTTCTCTGACTG[A/G]AATTGCAGTATGCTT	10391
rs549876935	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722581	CACCTCACTAAAGCG[G/T]TTTTTTTGACAAAAG	10391
rs549889662	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68628587	GCTACATGTATTAAG[A/C]CCATGGTATGAGCAA	10391
rs550002523	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68605817	GCAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC	10391
rs550014915	snp	G/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68619174	CTTTTTACTTTGACT[G/T]CTAGGAAGCCCAGAG	10391
rs550035835	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726509	CCCGACGAGGACAGC[A/G]AGCGGCCCGGCTCCT	10391
rs550037175	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68626482	TGGTCCTGAGTGCTA[C/G]AGATTCAGACAGGTG	10391
rs550043692	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68594869	ATCCAAATAATAACA[A/G]TTGAAATCTCAGCCT	10391
rs550053592	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	CORO2B	GRCh38.p7	15:68616614	ATGATTCTGACAAGC[A/G]GTGAGTACGGCTGTG	10391
rs550066952	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68650876	GTGCAGGGTGTGCAC[A/T]GGGTAAAGACGAGGG	10391
rs550087581	in-del	-/A	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68711250	CCCAGGCATATCCTC[-/A]AAAAAAGGTGGGCTG	10391
rs550090665	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616157	CTGTGCTTTTGTAGT[A/T]AACAGTATAATGATG	10391
rs550092679	in-del	-/CACA			intron-variant	CORO2B	GRCh38.p7	15:68704077	ACACACACACACACA[-/CACA]AATACAAATATTAGC	10391
rs550150569	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68589965	GCCTCCACAGTGGCC[C/T]GTGACCCCCGGCTCT	10391
rs550151332	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68697986	GTGGCGGGAAGGGCT[C/G]ACCCCAGCTGGTGTC	10391
rs550154338	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677996	CTCGGAGGCCTGGTG[C/G]GGCCCAGCCCCCTGG	10391
rs550168267	in-del	-/T	0.00159808	0.0282221	intron-variant	CORO2B	GRCh38.p7	15:68688208	TGTAATAATATCTGT[-/T]TTTTTTAATAACAAT	10391
rs550196743	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68720234	CCTGGCTGTGACTGA[A/G]CAAGTCTACTGACCT	10391
rs550204083	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684951	GAGAGCCAGGAAGAC[G/T]ATAAGCAACCTAATC	10391
rs550227245	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562097	TAATGATGTTGTCCT[A/C]CAGCCACCCCTTCCC	10391
rs550236583	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589524	ATGTACAGTAGAAAC[A/G]CCCATTTTGCAGAGG	10391
rs550264180	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68561703	TTGTGACTGTGCTCT[A/G]TCTGTTATCGTGTAC	10391
rs550267385	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691937	TAATGCACACAGCTC[C/T]GCTCAGGGAACACTC	10391
rs550269811	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68645007	CCCTGAATTCTTGGA[C/T]GCTTCTTCCTTTCCA	10391
rs550328511	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652236	GTTGTGAAGGCCAGT[G/T]CCTGTTTTTTCCCCT	10391
rs550351717	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68602679	TCCGTTTATTGCCCC[A/C]CCTTGAGGTAGGGAT	10391
rs550363165	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699629	ACAGCCCTGAACCGC[A/G]TCTTACCCGGGTGTC	10391
rs550370525	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68665274	GATTCAGGCTTTGCT[A/G]CATTCTACATTTCTG	10391
rs550373264	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560947	CCCATGGCACAGCCC[A/G]GGTAATTTTCCCTAG	10391
rs550412882	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68567757	CTGGGCACGGTGGCT[C/T]ATGCCTGTAATCCCA	10391
rs550422063	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68656968	CACCCTCCCCACCTA[A/G]GGTCCAGTCCCCCCG	10391
rs550455656	in-del	-/TGT	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68569289	CCTCTGTGCTCCACC[-/TGT]TGTTCATCCCTCCCC	10391
rs550460598	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560398	CTCCTGGGCTCAAGC[A/G]ATCCTCCCACCCCAG	10391
rs550472542	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68703081	ATCCACCCGCCTCGC[A/G]TCCCAAAGTGCTGGG	10391
rs550501662	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631002	CTAGGTCTCACTTGC[C/T]AGAACTGGGTCTTGG	10391
rs550509580	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68652707	CTGCTCTGTTTGAAT[C/G]TCACCTCAAGTTCTA	10391
rs550520521	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617429	TTGGTTCTAGTCCCA[C/G]TTGTGCTACTCACCA	10391
rs550529571	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68656345	CTTTCCATTCCACTC[A/G]GCCAAGACCTTGATT	10391
rs550538972	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575647	AGTGAGAATACACCT[A/T]TATACTGGTGTATTC	10391
rs550547716	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68608180	ACCCAAACCAGACAT[-/G]GGGGGCCTGAGCACG	10391
rs550558101	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605505	GAATATTCTGCAGCC[A/G]TTAAAAATTATAATA	10391
rs550597283	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700075	CAGCACTGCTGCCAG[C/G]GCCCTTCCCACGGCC	10391
rs550597701	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578137	GTCCCTCAAATCTCC[A/G]CAGCAGCTCCAGGAC	10391
rs550597775	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706424	GCTACTCAAGAGCAG[C/G]CATGGGCAAGTTCAA	10391
rs550606766	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716956	ATTATGGGGAGGGTT[A/C]TTTTTCTTGAGTGGG	10391
rs550612680	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68684206	GAAGTCTGCCTGAGA[A/G]TCTAAAAACCCCAGG	10391
rs550664066	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68635191	CTCCCCACTGGTCTT[A/G]AACCACCCATTTGAT	10391
rs550671615	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711907	GTGGGGAGGGACCTC[A/G]TACCCTTTCCTGTCC	10391
rs550680194	snp	A/C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618116	CATTTTGTTGTGACC[A/C/G]AATACACACACATGC	10391
rs550767651	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68680168	TGCCATGTGACTCAC[G/T]CCCACTTCAATGACA	10391
rs550778602	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68571994	GGAGAGAACTCCTGA[A/G]GGGGGCAGACACAGA	10391
rs550824450	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667347	GCCAACAGACTCTCC[A/G]CTTCCTGCCATGTCC	10391
rs550825423	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711230	GTGGAGCCTCAGCCC[C/G]GAGCCCCAGGCATAT	10391
rs550827237	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68704451	TGAAGACAGATGTTC[A/G]GAGAGGCTAAGAAAC	10391
rs550833526	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630700	TTCAAACAAGAGTTG[C/T]GGAGGAAGGAGGTCC	10391
rs550836380	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625865	CCCCCTTGGCCTCCC[A/G]AAATGCTGGGATTAC	10391
rs550865099	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718205	CATAGAACAGAACAG[C/T]AATCTTAGGCTGCGT	10391
rs550919213	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583608	TGGGAGGAGGGACAG[A/G]ATGTGGGGCAGGGGA	10391
rs550946103	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660122	TCTAAAAATGTTTCT[A/G]TATGGTACCAATTCT	10391
rs550973508	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68723908	GGCAAGACTCTATCC[C/T]TAAAAAATAAAAGTA	10391
rs550981337	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68692170	CTTGACCTTGGGCAA[A/G]TAGCTTAACCTCTCT	10391
rs550996252	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68699324	ACCGAGTGTGGTGCA[A/T]GGGAGACACTACACG	10391
rs551028931	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568690	TGAGTGATTTTGCCC[C/T]CATTTTTTAATAGAT	10391
rs551051686	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591529	AAGCAAAGGAGTGAT[A/G]TGATCCCATTCACAC	10391
rs551060953	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68718546	GAGACTGATTGAAGG[C/T]GCCCCGGTCTACCCC	10391
rs551065265	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604301	TACCATCAGGAAATT[G/T]GTTCCATTCTTCATG	10391
rs551110519	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657845	TGTCTCCTACCCAGA[C/T]TCACAAACCTCCTAA	10391
rs551158101	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671734	ATAGGCTAAGTGTTC[C/T]CACTCATGGCAGCTG	10391
rs551248243	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68612192	TGAGGATCTTAGAAG[C/G]TCTGGATGCAGATGC	10391
rs551281653	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639802	CAATCTTGAAAACCA[A/G]TCTCAAAACCAATAT	10391
rs551306968	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68645750	CTAGCCATAGGTATT[A/C]TACATTGAGCATCTG	10391
rs551315440	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68658398	CTGTGCCTCCTTCCT[A/G]CCTTCGGCCAGTGAG	10391
rs551316688	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68582827	CTTATAGTGACCAGG[C/T]TCCCCTATTTTGAGG	10391
rs551343386	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630280	CATGAACTTGACTAT[C/G]GCTCCCTCGACCCAA	10391
rs551345027	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68639018	TGGAGACAGGGCTGC[A/G]TGACCAGAAGAAAGA	10391
rs551386877	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68705042	CAGGCCCACTGTGAA[C/T]TCCAGCTCCTCCTCT	10391
rs551438583	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718112	CCATGATAGACGTTC[A/G]GCAGAGGCAGCTGTT	10391
rs551462325	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575424	CTCACTGCAACCTCC[A/G]CCTCCCAAGTTCAAG	10391
rs551479996	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591710	TCACATATGCCCCAC[C/T]CCATACCCTAAGATG	10391
rs551495873	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617398	CCCTTCACTGGTAGT[A/C]TGGGAACCAAAGGAC	10391
rs551511228	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576475	CCACAACAACGGCGG[A/G]TGGCGGGAAAGGTGC	10391
rs551518887	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68591072	GGGGGATCCTGGTCT[A/G]TGGGGGGACACAGGC	10391
rs551523026	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578334	AACGGCTCGGGCAGG[C/T]AGGTCCTGTGCTGTG	10391
rs551538238	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68607707	CTTGTGGTCCCAGCT[A/G]CTTGGGACGCTGAGG	10391
rs551539594	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68625202	GAATCTCTAAACTTG[A/C]AGCTTTTCCACAGTT	10391
rs551565963	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678401	AGAAAAGACAGCAGG[C/T]GGTGGTTCACACCTG	10391
rs551607096	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597704	CTATGGAGCTCAGAG[A/G]CTTCACCAGGGTTAC	10391
rs551612976	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68692871	ACTCCTGACCTCAGG[C/T]GATCCACCCGTCTCA	10391
rs551629940	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68641769	CGGCACTGTCGCCCA[C/G]GTGGTAGTGCAGTGG	10391
rs551643358	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597130	CTCATTTCAAATTGC[A/G]TAAAACCAAAGAGCA	10391
rs551656118	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68723280	GTACCCACCACCATG[C/T]CTGGTTAATTTTTGC	10391
rs551669273	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68675820	TACTGAGCACCTTCT[C/T]TGTACCCGGCACTGT	10391
rs551675309	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699490	TGAAGGGAAGGGACA[C/T]GGGCTTGGGGCACAG	10391
rs551677019	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722486	GAGGGAAAAGTCCTA[C/T]GATTGTACAACTCAG	10391
rs551678887	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68716131	AATGGAAACCAAAAG[A/G]TGTCCGAAGTCCTAA	10391
rs551698130	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562010	TGTCCCTTCTCTACC[C/T]TAAAGGCAGGCCAAC	10391
rs551698656	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629621	GGGAAAGGCTATGCA[C/T]TGAGCAGCTCCCAGG	10391
rs551725198	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640869	AGGAGGAGCAACTGG[G/T]GCTTGGAGCAGCAAA	10391
rs551734280	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68685889	TGGCAAGCTCTAGGC[A/G]GAGGAGAGAGACAGG	10391
rs551740741	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721890	GTAGCTGGAACTAGC[A/G]GCGTGTACCACCATA	10391
rs551797518	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68646145	TCCCCATCCCCCACC[C/T]CCTATCTAAAGATTT	10391
rs551798352	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667133	CCCCTAAGGCCTCCC[C/T]TTCTGGATGAAGTCC	10391
rs551803255	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601515	TGAGCGTGCAGTGCG[A/G]GGAGGGCTAGGATGA	10391
rs551809377	snp	C/T	0.000399281	0.0141238	intron-variant, splice-donor-variant	CORO2B	GRCh38.p7	15:68632343	AGGAGCCCCACCTGG[C/T]AGGTAGCAGTGATAA	10391
rs551810438	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68673538	AAATAAAATTTTCTT[A/G]AAAAAGGAAAGTGTC	10391
rs551837880	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68623594	CATCTCAGGGCAGTG[C/T]GGTTGACTCCTGGTG	10391
rs551861556	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694542	CAAGATGTACACTGC[A/G]GAAGGACGCTCATTC	10391
rs551876165	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68672763	GAGGAGATACATCAG[A/G]CAGCAAACCAGGCCC	10391
rs551880389	in-del	-/ACCAAAAA	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68722600	TTTTGACAAAAGTGG[-/ACCAAAAA]ACAATGCAAAGAAAT	10391
rs551900159	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646446	TGTCAGCTGGTGGTG[A/G]AGGATGGATTTTTCC	10391
rs551911113	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639750	GTTAGGCAGCTCTAA[C/T]CATTAAGAAAGTCCT	10391
rs551936047	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68599921	TGCATCATAATGAAC[C/T]GCGTCCTTGGAGACT	10391
rs551936576	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68686554	GGACTATAAGGATTT[A/G]ATAAAACCTTATAGG	10391
rs552036985	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604776	TTGCCTTTCTAGATT[A/G]TGCATTTTTTACTTT	10391
rs552049521	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612142	TTGTTTATCGGAGTA[G/T]ATTCCCAGGAATAGA	10391
rs552049650	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68619908	ATGAAAGTGGAGTCA[C/T]GTTTTTTTTATTTTT	10391
rs552057689	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712367	CAGAAAGTTTTCTAG[C/T]ACTATAGGTTGAGCA	10391
rs552085983	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68619189	GCTAGGAAGCCCAGA[G/T]CCCCAATCTGTGTTA	10391
rs552095778	snp	G/T	0.0263992	0.111815	intron-variant	CORO2B	GRCh38.p7	15:68605720	TCTTGGGTTTTTTTT[G/T]TTTTTTTTTTTTTTT	10391
rs552107640	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68652912	ATAAATGTGCCTTGT[A/G]TTACTATTACTGCCA	10391
rs552128735	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68558736	GGAGTGTGGACACGG[A/G]GTCACCCACCTCCTT	10391
rs552134740	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689177	TGCCCACAAGAACAG[A/G]GTGAAGATCTCCCTA	10391
rs552146315	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644178	CACTCATGCAAAGTC[C/T]GCTATGGATTCTGTA	10391
rs552162374	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593110	TCATTCTTTCATCAG[C/G]AGCCCACTCCCAGGA	10391
rs552184254	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68708776	CCTTGAACTCCTGGG[C/T]TTAAGGGATCCTCCC	10391
rs552191787	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705551	TCTCCCTCTCTGTGG[A/G]ATATTTATTCATCTG	10391
rs552198063	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68695530	ATTTAAAAATTAAGC[A/G]TGTGATTCAGCATTT	10391
rs552211345	snp	C/T	0.00557542	0.0525036	intron-variant	CORO2B	GRCh38.p7	15:68591500	GGTGTTGCTGGGAGT[C/T]CTAGAGGGGCTTTAA	10391
rs552233771	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68599235	CTCTGATCTCTCCTT[A/G]CTCCAAACTCTATCC	10391
rs552246792	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655454	AGAGTCAGAGGGGAC[C/G]CCAGGGATCATAGAT	10391
rs552258847	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68687755	GCATCTGGCAACGGC[C/T]TTCCTGCTATGACAT	10391
rs552290302	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68661592	CTGACTACATTTGCA[C/T]AAAACAGTAGAGTTA	10391
rs552319225	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694138	ACCGCACCCGGCTTG[C/G]TTGTGTTATAATGGA	10391
rs552329969	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68718234	GTCCAGACCTCTAGG[G/T]TGTATGGGGAATGGC	10391
rs552347496	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668827	CTCACGCCTGTAATC[C/G]CAGCACTTTGGGAGG	10391
rs552347912	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586693	CCAGACCCGGACCTC[C/T]GGATTCTGGCCTCTT	10391
rs552361616	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668225	GAGAGGGCCTAGGTC[A/G]TCTGCCCCACAACGT	10391
rs552380970	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563230	CCATGGCTCACACCT[A/G]TAATCCCAGCACTTT	10391
rs552391144	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68696651	ACTTTCACCAGTGGA[A/G]GTAGGGTCAGAGGGC	10391
rs552428423	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68698856	ACCCCTAGTAGAGGC[A/G]CAGAGGGGCAGGGCC	10391
rs552436281	snp	A/T	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68678451	GGCCGACTTGGGCAG[A/T]TCACCTGAGGTCAGG	10391
rs552441313	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68602157	ATTCAAATCACAGCA[A/G]CCATCATAATCCCAT	10391
rs552474893	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68603525	TGGGCTGAATTGTAT[-/C]CCCCTAATTCATATG	10391
rs552504591	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68570259	TGAGTGTAACTTCAT[A/G]GGATCCTCGGAAGGA	10391
rs552513283	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627521	GGACTCTCTTGGGGT[G/T]GGGGAGGTGGAGGTA	10391
rs552542482	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667814	AGGAAAGAGACTTCA[C/G]ACCAGTTACTTCCAT	10391
rs552545088	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608092	GGTGAAATGCCACCA[A/G]CGTGAAAGAACATAT	10391
rs552599492	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679585	GTGGTGCCAGGCCCC[A/G]TGCCCAGTGAGTTTG	10391
rs552691833	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68645078	CACCTCTGAGCCGCA[A/G]CTTCCCTCCCCCAAG	10391
rs552725618	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68707503	TCAATTAATAGAGGT[C/T]GATTATATTCATCAT	10391
rs552733855	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613929	GTTTAGCTTCCTTAT[G/T]ATAGATTTAGTTTGT	10391
rs552735480	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68584001	GCGGCTAGCAGTCAT[G/T]CGTTCATTTAGCCAG	10391
rs552765021	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651920	GCAGAGTAGGAAGCC[A/G]TGTCTACAACAACTA	10391
rs552776363	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68590391	GCACTTCTGTTCTCT[A/C]AGGTACCCCCATAAC	10391
rs552804588	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674876	AGTCCACAGTGACCA[A/G]TATTATCTCCCACTA	10391
rs552835400	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68638307	TCACAGGAGAAGGAG[A/T]GAGGGTAGAGCTAGT	10391
rs552875495	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633909	ATCTTTTTCTGCATT[A/G]CCAGGTGACAGGGAG	10391
rs552879955	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651270	TCCCTCTACCGCCCC[C/G]TGTGGTCAGGGCTGG	10391
rs552889537	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68584855	AGGCCTTGCCAGGGA[A/T]GGACAGATGCAAATC	10391
rs552916319	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631972	GCTGGAGTGGGCTCT[C/G]TCTTGGTTGCTAGCA	10391
rs552927802	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586649	AGTCACCTGTAAAAG[A/G]TGGCCCAGTGAGGCA	10391
rs552956415	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717871	ATGTGGTCTGTGCTC[A/G]TCACGGTGCCAGGCA	10391
rs552957568	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598805	ACGCTGCCAAAAGAA[A/G]GTTTCTGTTCTGTCC	10391
rs552965330	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68704526	ACAGAGCTGTCAGAC[A/C]ACAAAGCTTCTTGCT	10391
rs552977687	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591361	ACATGTTTGGCTTAT[C/T]CTAGGAGAGAACCAG	10391
rs552977941	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68694400	AAACCGAGGCTCAGA[A/G]AAGTTCATTAACTTT	10391
rs552996359	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68587596	TCACCAGGTGCTAGG[C/T]CCCTGCTTTCAAGGG	10391
rs553017787	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68723536	CTCGGCTCACTGCAA[C/T]CTCCACCTCCCGGGT	10391
rs553023729	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68610568	TTCCATCACAAAGCC[C/T]CTCCTCCAGCATCCT	10391
rs553039489	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700747	GGCGGCAGGGAAGGG[C/T]GCTATCGGTTTCCAA	10391
rs553062639	snp	C/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68592080	CCTCTTCCCTTCCCC[C/G]GTGTCCCCAGACTCT	10391
rs553127668	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687315	TGATTCTCTAGGTAA[C/G]AAAACATTTTGCTTC	10391
rs553130149	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722907	ACCCTGTCTCTACTA[A/C]AAATACAAAATTAGC	10391
rs553143607	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570573	CCCACAAAGTGAGCT[A/G]ATCAGAGGAACCCCA	10391
rs553153620	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68721476	GTTGAGAGGCCAAGG[C/T]GGGTGGATCACCTGA	10391
rs553165687	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561779	TGTGCCTGTGTGAGC[A/G]GAGCATGTTTCCGTG	10391
rs553175432	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68597376	CTAATTGTTTTACAC[A/G]CACCTCATATCACCC	10391
rs553223600	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68673759	GGAGAATCACCTGAA[C/T]GGGGGAGACAGAGTT	10391
rs553227071	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68611093	AATGCGCCCCACCAC[A/T]GAGCCACTGAGCATG	10391
rs553230420	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68666964	ATTTGGCTCTGGGCT[C/G]CTTCCTGGGCAGTGA	10391
rs553252951	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68576908	CTGTGCTCAGAGGCT[C/T]ATGAAAATGAGACCA	10391
rs553253631	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568824	CACACACTGGGGCCT[G/T]CCAGCCAGGAAGGGG	10391
rs553261640	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68658147	TGAGATGTTGGGCCC[A/G]TTGTCCTCCAAGGTC	10391
rs553270429	snp	C/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68576738	TCTTCCAATGCTGGA[C/G]AGCTCGCTGGTGGGA	10391
rs553281335	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562603	ACAAAAAAATTACTC[A/G]TTGTTTCTTGAAATT	10391
rs553293923	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699079	GGAAGAGACCCAGTA[C/T]ATCCGGTGTGCTTGG	10391
rs553304217	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68704603	GTAGCTTTATTAACT[C/G]TCCTTATCAGCTGCC	10391
rs553309874	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68612009	CTCCTGGGCTCAAGC[A/C]ATCCACCCACCTCCA	10391
rs553323936	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68636924	CCACATGTGCCTATT[A/G]AGCACTTGATATGTG	10391
rs553363476	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68666631	CCCCTGAATGAGCTC[C/T]TCCTGGAGAGCGAGG	10391
rs553394734	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68685610	CAGGTGCTCCAGGAG[A/G]CAGGAGGCCCAGGCC	10391
rs553401738	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68707811	GAGTTATGTACTCGC[C/T]AGCTTGTTCCCCCTG	10391
rs553415863	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722683	AAAGGCAAATAGCAC[A/G]TCATCCCTCTCAACA	10391
rs553420069	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653794	TCGTTCCCATTCCAG[A/G]TTTCTGTAACACCCC	10391
rs553432743	snp	A/G	1.80468e-05	0.00300384	intron-variant	CORO2B	GRCh38.p7	15:68711524	CTGACCCTGCCTCCC[A/G]TGCATCTGCCCTCGC	10391
rs553435676	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68562918	GGAGGTGGAGCTTGC[A/G]GTGAGCCGAGATCAT	10391
rs553457643	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707662	AGTATCCCTTCTGGG[C/T]AAAAAGAAAGAAGTG	10391
rs553484104	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661783	AGGCCGAGGCAAGTG[A/G]ATCTCTTGAAGTCAG	10391
rs553495200	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68627347	ACCAGGGCAGGGCAA[C/G]TTGCCCTCAGTGCCT	10391
rs553498965	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705953	ACCTGGGCTGGGGCT[C/T]ACTCCACAGCCCCCC	10391
rs553503345	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68719337	CTGTTTGAACTTCCC[C/T]CCCACCCAGCCTGCT	10391
rs553528843	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618298	GGAGGTGACCCTCCA[A/G]TGTGAGAAACATGGG	10391
rs553532195	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627027	GTCCCACCACTGCCA[A/G]GTGGGGATCCTTAGC	10391
rs553536800	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653132	TGGCAAGGAGAGGCA[G/T]GGGTGGGGTCCTGGA	10391
rs553541638	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667429	CTTCTAGGCGATGGG[C/T]TCCTTGAGGCTGGGA	10391
rs553564841	snp	C/G	2.00785e-05	0.00316841	intron-variant	CORO2B	GRCh38.p7	15:68718857	GGGCCTGCATCGCCT[C/G]TTAGCCTGCTCACCA	10391
rs553566710	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725760	GGCACGGGCGGCAGG[C/T]AGCTGGAGACTCACC	10391
rs553611214	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712017	ATCCCCAGGTGTTAC[C/G]CAGGTCCACCACAGG	10391
rs553640341	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712803	TAACCTTAGCGAAGT[C/T]GGGAGACTCGAATCT	10391
rs553657740	in-del	-/C	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68597019	CTCAGGGACCGCCCT[-/C]CCCTGCCAGCCTCAC	10391
rs553662101	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68625970	TTGCTCCTTTTATTG[C/T]TGAGTTTGTGTTCCA	10391
rs553667168	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68634039	CTCGGCAGTGGCAGC[C/T]ATGCCTGGCATCTCC	10391
rs553672410	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68686629	CACGGCCAGGTACAG[C/T]GGCTCACGCCTGTAA	10391
rs553683489	snp	A/C	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68623440	CCTGACGTGAGTGAC[A/C]GCCAGTCTGGCCCAC	10391
rs553725273	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654514	CTGAAGCATCTGGCA[A/G]TCTGCTTGATCTGCT	10391
rs553726413	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68707037	ACAATCTCGGCTCAC[A/T]GCAAGCTCCACCTCC	10391
rs553736974	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669645	TTTCAGGAAAAAAAA[A/T]TTCAACTTTCTAAAA	10391
rs553737559	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661235	CACCCACCTCGGCCT[C/T]CCAAAGTGCTGGGAT	10391
rs553742622	in-del	-/CT			intron-variant	CORO2B	GRCh38.p7	15:68707307	TGAAGCAGTCTCAGA[-/CT]CTGTGGGTTAAAAAC	10391
rs553748365	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625479	CCAGGCCTTGCCAGC[A/G]TTCATCCGTGTTCCA	10391
rs553749771	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68614228	AATCATCCAGATCTT[G/T]ATTGTTAAATGAGTT	10391
rs553768661	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701527	GTTTCGCTCTGTCGC[C/T]CAGGCTGGAGTGCAG	10391
rs553808342	snp	A/G	9.91015e-05	0.00703853	missense	CORO2B	GRCh38.p7	15:68713983	TGGGGAACATGAAGC[A/G]GCTCCTCACGACAGG	10391
rs553831877	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572063	GACTGGTCTGGCCCA[A/G]GGGCATCTGGGAAGG	10391
rs553891948	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642099	TGGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG	10391
rs553921707	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571263	CTCAGTACATGTAAA[C/T]ACAGATGCAACCAGC	10391
rs553929113	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68709117	GCTTCTACATTTTCC[A/G]TATAAATGATGTTGC	10391
rs553943024	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68647774	ACACTTTGGGAGGCC[A/T]AGGCAGGAAGATCAC	10391
rs553965611	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68648281	GAGGTTGCAGTGGGC[A/G]AGATTGCGCTACTGC	10391
rs553994529	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681142	CGCTTGAACCCAGAA[A/G]GAGGAGGTTGCAGTG	10391
rs553995600	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668052	CTAAGCTCTTGAGAC[A/G]CCTGGTGCCACTGAA	10391
rs554002783	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68633469	TCAGCTGGTGAGGCC[C/T]CTTGAATTGTTTCCA	10391
rs554021660	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726664	CAATTTGTGAGCCAG[A/G]CAGGGTAGGGATTAG	10391
rs554057676	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687847	AACAAACCCACTCAC[A/C]AGACAACTAACCCAC	10391
rs554058394	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68674655	CAGAGAAAGGCTCGT[A/G]GGCAGTGGCTTCTCC	10391
rs554078390	snp	A/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640522	TATTTAAAAAAAAAA[A/T]AAAGGTGATAGGAGT	10391
rs554095406	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68712105	GGAAATGGCTAGGGT[G/T]CCAAGGCTGATGGTG	10391
rs554133391	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694762	GCAGATCGTGGGCCT[A/G]TGTGTGTGCCACCAG	10391
rs554136675	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68559090	AGGGGTAAATACCTA[C/G]AAATGCGCGAAGTGT	10391
rs554162477	snp	A/G	8.27767e-05	0.00643284	intron-variant	CORO2B	GRCh38.p7	15:68714688	GGTGGGGGAGGGCCC[A/G]GGGCAGCCTGTGGGA	10391
rs554169012	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608285	TCCTGTGGCTGGCTG[C/T]GCATGGCCAGCCCAG	10391
rs554206870	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68628054	CAGCAACATCAGTGC[C/T]GGAGAGAAGAAGAAA	10391
rs554219497	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68723275	TACAGGTACCCACCA[C/T]CATGCCTGGTTAATT	10391
rs554292600	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626168	AAATGTTCCTACTGC[A/G]TGCTGCTGTGAGGGC	10391
rs554293353	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720862	GCCATCTTAAACTAG[A/G]CAGTCTATACCACCA	10391
rs554293482	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595059	TGATAGTATTTTAAG[A/G]GTCAGTTGAGTTGTG	10391
rs554298384	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68724975	CAAACTTTGGTATTC[C/T]TGTCATAGTTCCTCA	10391
rs554329268	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632811	TGGTCAGGCTGGTCT[C/T]AAACTCCTGACCTCA	10391
rs554339238	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680559	CTGATTAGGTCCACC[A/G]TCTATGGCATCATTA	10391
rs554354590	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720318	AAAGAGATAATTCAT[A/T]AGTGTCTAGCACTCT	10391
rs554378701	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68689362	ACAATTCTGTGAGCC[A/G]ACCATCTGAACAGTC	10391
rs554383962	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68602318	TAATTTTTTTTAAAC[A/G]CTCTTGGTGCTGTGG	10391
rs554397473	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68650776	TACTTAACGTTTTGT[A/G]CTTTCGAAAAAATAG	10391
rs554418243	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68601397	GCGTTGTCAGGTGCT[A/G]TGCCTTTCGGTAGGC	10391
rs554430887	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640388	TTAGACCTAACTCTT[A/C]AAGTTTACAAGGGAT	10391
rs554434900	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592651	TCTGCATCTATTCAT[A/G]TATTCATTCACTCTA	10391
rs554443140	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68674010	AAGTTAGAAGGAGGC[A/G]GATTTTCATCTCATT	10391
rs554452285	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558379	TCCCCCTCACCATTT[A/T]TTTTTTAAGACAGGG	10391
rs554497813	snp	C/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68695745	GTGTCCTGATTTTTC[C/T]AAGGACCCACACAGG	10391
rs554509924	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701893	TGTGTCCCCTAAGAA[C/T]TCCATAGACATTAAC	10391
rs554521332	snp	A/C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675916	CGCTAGCGGAGGAGA[A/C/G/T]AGATAATAAAGTGGA	10391
rs554582413	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68682196	CCCAACTGCCAAAAA[A/T]TCCTGCAGATAGTTA	10391
rs554584895	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633973	AGGCACTCTGAACAC[A/G]GGATCCCGGTTATCC	10391
rs554596288	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598194	CCTGGGCTCTGTAGG[C/T]AGCCCCTGGAGAAGA	10391
rs554607376	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68659744	TTCAAGACCAGCCTG[G/T]CCAACATGGCGAAAC	10391
rs554612008	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674542	GTGTGGCCTGGCACA[A/G]CCATCACCCTCTTAC	10391
rs554628361	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68600143	ATTGTTGGCTGAAGA[C/T]TTCTTCAACAAACAA	10391
rs554634554	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587648	CAATAATAATAGAAG[C/T]GGCTAACCCTTCCGG	10391
rs554651629	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578672	CCAGCCTGTGACTTC[A/G]CCAGCGTCCCCGGGC	10391
rs554662915	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68569878	GAAAGGCTTGCCCAG[A/G]GAGTGGCAGAATTGC	10391
rs554671602	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68594398	GCGCTTTTGGTACAA[A/G]CTGAGCTGTGCTCTC	10391
rs554676790	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68651745	TAAGAGATTTGGACC[A/T]GAAGAGAACAGCACC	10391
rs554688315	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577808	TATTATTGCTCCAAT[C/T]TAGACACTGGTCTCC	10391
rs554742128	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558263	AAGCCCAGCTTCTCC[A/G]GAAGCTGTCTGCTGC	10391
rs554752847	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68591877	CATGGCGAGAAGAGC[A/G]CTGGAATGGGATTTC	10391
rs554756406	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654433	AAATTATAGTAGCTG[G/T]TTCACTAGGACTCTG	10391
rs554782324	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68681106	TAATCCCAGCTACTC[A/G]CGAACCTGAGGCAGG	10391
rs554789904	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68695662	TGCAGGCTGGGCAGG[C/G]TAAATGTACCATCTG	10391
rs554824485	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640023	CCCCGGTTACAGCCT[C/T]GGCAAGGCCTCCTCT	10391
rs554843994	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687783	CATCCCATGGCAGAA[A/G]GTGGAGGGCAAGAGA	10391
rs554856020	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68687187	AGGGTCTGGGAATCT[C/G]GGAAGCCCAGAGAGG	10391
rs554870481	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68651788	CCAAATCCCTGCCCC[A/G]AGGCCACACCTCCTG	10391
rs554871531	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693794	TGCTCACAGACAAAC[A/C]GAAACAAACTGCAAA	10391
rs554885887	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68646079	GCACCTGGCCCACTC[A/G]TTTTTTTTTTAATTG	10391
rs554900749	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68683617	TGGGACTGGATATTG[A/G]GAGCCTCACCTTCCC	10391
rs554917042	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614159	ATATATGTCTCTGTG[C/G]CAGGGAGAACCTGTG	10391
rs554986632	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68605115	CGAGACTCCGTCTCA[A/T]GGAAAAAAAAAAAAA	10391
rs554989207	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635046	CGGGAGCCTGCATTT[C/T]CACAAACACTTCAGG	10391
rs555002398	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68621144	GTGCAGGTGTAGGGA[C/T]CCTCAAGGCCATAAG	10391
rs555007277	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68704801	CCTGTAAAGGGGACA[A/G]TCCCCAGCAAGGCAG	10391
rs555021953	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726112	CCCGCCTACCACCTC[A/G]AGAACTGGAAGCCAA	10391
rs555033709	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703213	TGTCATGCAGTGGCG[C/T]GATCTCAGCTCACTG	10391
rs555039506	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68593540	TCTCTAGACACTTGT[A/G]ACTGAGCTGGAACAA	10391
rs555040090	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609002	TATCCTCAAGGTGCA[A/G]CAGAGAGGAAATCAA	10391
rs555073107	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68634270	ATGACAGTCTAGAAA[G/T]GCAGAAGAAAGCCCT	10391
rs555094580	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697383	AATGAAAGATAAACA[C/T]ATGAACAAGTAAATT	10391
rs555097207	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68647389	AGAGTTCCAGAAAAA[A/T]TAACAAGAAAAAGAA	10391
rs555100892	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559842	AGCAGGTCTCCCGCA[A/G]ACGCGCGCGCACGGA	10391
rs555102201	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68573772	AGCCGGGGATGCTTC[A/T]TTCTCCAGGAGCTTG	10391
rs555108466	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708319	TCCTAGCCTTGCTCC[A/C]AGGACTTCTGGTCTG	10391
rs555130265	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68600314	CCTTCCTCAATGTTT[A/G]CATCTTTCCCAGCCC	10391
rs555130626	snp	A/G/T	6.64246e-05	0.00576268	missense	CORO2B	GRCh38.p7	15:68725850	CACCCCAGCTCCTTC[A/G/T]AATGTTCTTCCGGCA	10391
rs555134024	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68682205	CAAAAAATCCTGCAG[A/T]TAGTTATGTATGCCA	10391
rs555186279	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572996	AGATACATACAGTCC[C/T]ACACACTCATTCTCA	10391
rs555188314	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68581351	CTTGCTGGCCCTTCA[C/T]AGACCAGCGTGTTCT	10391
rs555193982	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68619798	AGCAAACTCAGTGTG[A/G]ATAGTAGGACCAGAT	10391
rs555216505	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68607546	CTTTGGGCCAGGCAC[A/G]GTGGCTCATGCCTGT	10391
rs555224840	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580592	GAAGATGAACTTGAG[C/G]GTGCAGGGGCTTCCT	10391
rs555277244	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613404	AAATTAGGGTTCATC[A/C]AAATAGATTGAACCT	10391
rs555297624	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642190	TACAGGTGCCTGCCA[C/T]CATGCCTGCTATCCT	10391
rs555300304	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68701462	GACTACAGGCGCCTG[A/C]AACCACGCCCGGCTA	10391
rs555312295	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707110	GGATTACAAGCGCGC[A/G]CCACCACGCCCAGCT	10391
rs555333821	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657473	CAGTGAGCTGTGCTC[A/G]TGCCACTGCACTCTA	10391
rs555351499	snp	C/T	1.64866e-05	0.00287106	synonymous-codon	CORO2B	GRCh38.p7	15:68714651	CACCCACATGCTCTA[C/T]CTGGCTGGAAAGGTA	10391
rs555353825	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606933	GTGGATTGACTCGGA[A/G]CCAGGAAAGGGGCAA	10391
rs555372945	in-del	-/CA			intron-variant	CORO2B	GRCh38.p7	15:68704079	ACACACACACACACA[-/CA]AATACAAATATTAGC	10391
rs555377181	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68688917	ACTCATCCTGGAGCA[C/G]GGCGTCCATGCCCTC	10391
rs555392689	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68580868	CATGCAGCCTTCCTT[-/C]CCTGGAGGCCTGCAA	10391
rs555397972	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68610932	TCCATTCCACACCCT[C/T]GACGCAGCCAAGGAA	10391
rs555400936	in-del	-/TTGTTTGTTGTTTCTTGTTTTGGGT	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68625591	TTACAGGTTTTTTTC[-/TTGTTTGTTGTTTCTTGTTTTGGGT]TTGTTTGTTGTTTCT	10391
rs555403267	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68623816	TGAGGTTGGAGGCGG[A/G]TGTGTTTGAGCAGCC	10391
rs555410302	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68621177	ATGTAGCCACAGCGT[C/T]TAATGAGCAATTGAG	10391
rs555418533	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68649460	AGGAAATGGGGTAAA[A/C]AAATTAGGGAAGAGC	10391
rs555433551	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568232	ACCCAGGACAAGTTA[C/T]TTCTCCTCTCTCCCT	10391
rs555480677	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68664564	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA	10391
rs555489453	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630384	AGCACACCCCAAGGA[A/T]CGGTGCTGAGGGATG	10391
rs555493423	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68584597	CAGGGCTGGTGGAGT[C/T]TCGGCTCCTGGCACC	10391
rs555495734	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722044	AGTCATGAGACACTG[C/T]GCCCAGCTATTTTCT	10391
rs555502931	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617134	TGTCAGCCTTCAAGC[C/G]CGTGCTTTCCAACAA	10391
rs555524854	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629726	CAGATCAGGAGGACT[C/T]GGACGAGGCTGAGGC	10391
rs555554094	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709653	GTAGAGGCACGGTCT[C/T]GCTGTGTTGCTCATG	10391
rs555555329	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721636	ACTTGAACCCAGGAG[A/G]CAGAGACTAAAGCTG	10391
rs555557639	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68728024	CCTGTACATTGTAAG[A/G]TATTTAGCAGTATCC	10391
rs555591136	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564694	TGATAGAGTCATTGT[A/G]AAGATAAAGAAATGG	10391
rs555597072	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68560472	GCTAATTAAAGACAA[-/T]TTTTTTTGTAGAAAC	10391
rs555599352	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621912	TAGGCACATGCCACC[A/G]TGCCTGGCTAATTTT	10391
rs555650314	in-del	-/TATA			intron-variant	CORO2B	GRCh38.p7	15:68619679	ATGTGTGTGTGTGTG[-/TATA]TATATATATATGTAC	10391
rs555666198	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727536	TTTCCCATGGCCGCC[C/T]TACGGAAAATCCCAT	10391
rs555673008	snp	A/C/G	0.000507335	0.0159191	intron-variant	CORO2B	GRCh38.p7	15:68714087	GCTAAAGGAAGCATC[A/C/G]TTGCCTCGGAGGTCA	10391
rs555722508	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68665362	ATTCATGTACCAGTA[C/T]CACAATGCTGTGTTA	10391
rs555723671	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68569418	GACTGGCTTCTCTCA[C/T]TTAGTGATATGCATT	10391
rs555727440	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589067	ATTAAAAGATCTGGG[A/G]ACAAACTCAAGTTAT	10391
rs555782159	in-del	-/T	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68712333	GTGTTTACCTTGGAA[-/T]AGTCCAATATTACAA	10391
rs555797044	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614718	AGCGGCTTCCTTTCC[A/G]TTCCTGCCTTGTGTG	10391
rs555803606	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648011	CCACCCTGGGCAACG[A/G]AGAAAGATCCTGTCT	10391
rs555842765	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575164	CCTCCCAAAAGCATA[G/T]CCCTGAAGTGCAAGA	10391
rs555843692	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68590185	GAGGGAGAGTGGGTG[A/G]AGGGAAGGGGAGAGG	10391
rs555879643	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583080	TCAACTGTGCCCTGG[C/G]CCCTCTTTCTGCAGG	10391
rs555909560	snp	C/T	1.66043e-05	0.00288129	synonymous-codon	CORO2B	GRCh38.p7	15:68714038	GATTGCCCTCTGGGA[C/T]CAGGTCAGCCACGGG	10391
rs555913370	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68670508	AGAATCATTAGTTTC[C/T]GTAGATGGATCAGAA	10391
rs555919143	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68702447	CGCCCCTCCTACCTC[C/T]CTGGGTTTGGTGGGA	10391
rs555926956	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68593227	CAATTAAATTTCAAC[A/G]TGAGTTTTGGCAGAG	10391
rs555964526	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684418	GTCTTGATTGGGATG[C/G]AGGGAGAGAAAGAAC	10391
rs555964540	in-del	-/A	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68681218	ATCTCCCTCCATCTC[-/A]AAAAAAAATTTTTTT	10391
rs555973463	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678076	CCTGCAAGGTCTGTT[A/G]CTTCCTGACAAAGGC	10391
rs555986147	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650896	AAAGACGAGGGGCCC[C/T]ATCCGCTAGGTTTGC	10391
rs556015854	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586830	ACCCCGATGCCTCAC[A/G]GAGCCTCCTTGGGCT	10391
rs556034798	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68613512	AGTCCCCTGGTGGCT[A/G]GCAAGGTTCTCCCTG	10391
rs556045032	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68677534	AGGCCAGATGGTGGC[A/G]GGGGGATGCTGAGGC	10391
rs556084397	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671530	CAAATTACCCCAAAA[C/T]GTGGCTGGGTAGTTC	10391
rs556086295	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68612740	TCATGATCCTCACGC[C/T]GCAGTCTCCTCCTCT	10391
rs556124144	snp	A/G	0.00835141	0.0640778	intron-variant	CORO2B	GRCh38.p7	15:68648370	AGAAACAAAAGGCCG[A/G]GTGCAGTGGCTCACG	10391
rs556127995	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68663459	GGTACGTGCTTTCTT[C/T]CAGGAAACACACACA	10391
rs556134613	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68655182	ACCACAGTGCCTGGC[A/G]TACAGCAAGTGCTCA	10391
rs556186111	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559171	GACCTGACTCAGTGG[A/C]GTCAGTGCTACTTCA	10391
rs556222799	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565135	AAATATTGCTTTACT[A/G]TCTACTGAACATGAA	10391
rs556233564	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726099	CAGCCTGAGGACCCC[C/T]GCCTACCACCTCGAG	10391
rs556240416	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636484	GGCGCCATCCCAGCC[C/T]TGCCTGTTCCCACTT	10391
rs556265597	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661878	CAGGTGTGATGGCGT[A/G]CACCTGTAATCCCAG	10391
rs556286979	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68670442	GCCTCAGCCTCTCAA[A/G]GTGCTGGGATTACAG	10391
rs556297708	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727512	GATGCATTATACTCC[A/G]TACCTGCTTTTCCCA	10391
rs556299492	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642668	CCCTGGTATCACTTC[C/T]TGCCATCACAGAGCA	10391
rs556300521	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68621268	ACTGCCTCCAGCCCC[A/G]TGGGACTCAGTCTGC	10391
rs556317986	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68587649	AATAATAATAGAAGC[G/T]GCTAACCCTTCCGGA	10391
rs556319629	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68681909	TATGCAGAAAGGGTT[C/T]AGGGGCTTCATAGAT	10391
rs556348105	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629702	GACACGAGCAGCCTC[A/C]GTAGGGGTCAGATCA	10391
rs556373984	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68579570	GATGCTGCATTTTTA[A/G]CCCCTGGAGAGCTGG	10391
rs556390798	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68622446	CTCTGAGTTGGAAAG[C/G]ATTCTCCAGTGTCAT	10391
rs556396155	in-del	-/CT			intron-variant	CORO2B	GRCh38.p7	15:68702025	AGGTGGGTGGATCAC[-/CT]GAGGTCAGCAGCTTG	10391
rs556416633	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68596994	GGGCCAGCAGGGCTC[C/T]GCAGAAGTCCTCAGG	10391
rs556435258	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68569127	TACAATCGATGAATC[C/T]ACATTAGCATGTCAT	10391
rs556463144	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68634907	AATGCCAGTGCTATT[A/G]GTCCACAGGCAGTCC	10391
rs556464845	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608895	CAGCCTCCATCCATC[C/T]GTTCAACAAGTGCTT	10391
rs556503609	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68590359	TCTTCGGAGGCTGCC[A/C]CCCCATGCCCAGCCC	10391
rs556512957	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671251	CTGTATTTCCCAATT[C/T]TTCTGTTGTTGTTTT	10391
rs556542449	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589780	GGAGGAGGCACCTGG[C/T]TGGAGAGACTTGGCT	10391
rs556558098	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654403	TCTCATTCCTTGCAG[A/G]GCCAGGGAGGCTGGA	10391
rs556579356	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68685358	TGGGATTACAGGCAC[A/G]TGTCACCACATCCAG	10391
rs556598727	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68696612	GAAACTGTGTTCTGG[C/T]CACTCCTTCCTCAGA	10391
rs556606363	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68559997	GGGGAGAGCCTCAGA[C/T]GGCAATGCAGATCTG	10391
rs556642889	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68722839	TTGGGAGGCTGAGGC[A/G]GGAGGATTGCCTGAG	10391
rs556649456	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68716663	GGTCAGGGAAGGCCT[C/T]TCTGTGATGATGGTA	10391
rs556671035	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589006	ATAACTTTATCATCA[C/T]AAATCTTTCTTCTAG	10391
rs556677252	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68715782	TCCCTAGGCTCTCAG[A/G]CAGAAACCCAGAGAG	10391
rs556680811	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68595806	AGGCAGACGGGCAAA[A/C]AAATACGGATGAAGC	10391
rs556681193	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68581520	TCCTAAATTAGCCAC[C/T]AACAGGCTGTGTGAC	10391
rs556714362	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68665090	TAACCTTTTTACTAG[A/G]CCTTTCACTACTTTT	10391
rs556735317	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68561230	GGAGAGGGCTGGGCT[C/G]GGACAGTGGAAGAGC	10391
rs556738145	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726876	CTATGGAGAATGAGA[A/G]CTGGAAGCCACTGCT	10391
rs556751917	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657375	CAAAAAAATTAGCCA[C/G]GTGTGGTGGCATATG	10391
rs556772011	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68596749	GGTGTGGGAGGAGAG[A/G]GGTACAACACAGCAG	10391
rs556774114	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68560679	ACTGTCCTCCACATA[C/T]AACCCATCTTCCTCC	10391
rs556808706	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603713	GACACAGCAAGAAGA[C/T]GGCCGTCTGCAAACC	10391
rs556829244	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651227	TTGGAGCCAGCGCCG[A/G]CTTCCCCTGCCGCCC	10391
rs556836716	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68682989	CCAAATGGCGAACAG[A/G]AGGAGGGGTTTTTAT	10391
rs556838583	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690961	ACTGTGCCTAGCCTA[C/T]ATTAGCTTTCTCAGA	10391
rs556842212	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601497	AGGTGGGGATTGCGG[A/C]CATGAGCGTGCAGTG	10391
rs556850805	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690109	GTGACTATTACATTT[G/T]CATAGTGGAAATATT	10391
rs556864382	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664504	TACAAAAAATTAGCC[A/G]GCCATGGTGGCAGGC	10391
rs556885912	in-del	-/G	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68613073	CCTTCAGAGAAACCT[-/G]CTGCTTTCTGTCTTT	10391
rs556898039	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559782	GGCGTGCCCACCAGG[A/G]GGCGCGGCCCGCATC	10391
rs556918009	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597333	TCACTAATGCTTATT[A/C]AGCGCTTACCATGTT	10391
rs556940429	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644385	CTTATAAATGACATA[A/G]GAAGATCAGAGACTT	10391
rs556977583	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68692372	GGCGGATCACCTGAG[A/G]TCAGGAGTTCAAAAC	10391
rs556982858	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68609646	CCTTCCACTGCCAGG[C/T]CTGAGCCCGCTGTCC	10391
rs556984724	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68581619	TGATCTCTAGGGCCT[C/G]TTCTGCTGAGCCTTG	10391
rs556990628	in-del	-/A	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68713084	GGACTGTTGTGTGTT[-/A]GGAGGAAATCAAGTG	10391
rs557002348	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68574292	AGCATGTGGGCATGC[C/T]GCCTGGGGTGGCATA	10391
rs557010008	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68701070	CACACCCCCACCTCC[C/T]GAGCTCCGGAACCAA	10391
rs557040941	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68698916	TGAGGTCATTGCATC[C/T]ACCAAGGTCAAGCAA	10391
rs557044359	snp	A/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68705276	AACCTTATCTCTACT[A/T]AAAATACAAAAATTA	10391
rs557048011	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68607302	TGACTGGAGCATCTA[A/C]ACATGGTGTCTCCAC	10391
rs557054395	snp	A/G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68651874	AGCCAGCTTGCTTGA[A/G/T]ATTTCCATATTTATG	10391
rs557060077	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68720020	GAGCAAGCTCTTTTG[G/T]GGCAGCTCGGCTGGG	10391
rs557071161	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604147	TCCACAGGCATGAGC[C/T]GCCCCTCGTCGTTCT	10391
rs557081366	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604351	CCGCCTTTCCTACCA[C/T]GAGCAGAACAAGTGT	10391
rs557112605	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68693310	ACAGCAGGACACATA[C/T]TCTGAAATAACTCTT	10391
rs557122488	snp	A/G	0.00279162	0.0372561	downstream-variant-500B	CORO2B	GRCh38.p7	15:68728214	CTGGGTGAGACCAAC[A/G]CTCTACATTGGAACG	10391
rs557155861	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68568163	ATAAAGTTGGAGGTT[C/G]AGTACAGGCCACTGA	10391
rs557180865	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68584700	TGCAGATTCTCTCTG[C/T]GCCCAGCCCTGTCTC	10391
rs557197610	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679350	TCTGAGCACATGCAC[C/T]GGGGCAGCTGGCCAT	10391
rs557212100	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610501	GACCCCTTGCTCTTT[C/T]GCTCACATCCCCTCC	10391
rs557233794	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68703379	TGGTCTTGATCTCCT[A/G]ACCTCAAGTGAACTG	10391
rs557240737	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68602680	CCGTTTATTGCCCCC[C/G]CTTGAGGTAGGGATG	10391
rs557246077	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575096	CCATAAGAACCAGGG[A/T]CTTTTTACTTTCTGC	10391
rs557248880	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609962	CCCCAGGGGACCCTG[C/T]AATTGTGCAACCAGC	10391
rs557291998	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703902	AAAGTGCACATGAAA[A/T]ATATAACTTGGCCAG	10391
rs557303511	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68596661	GAGCCCAGCAGCCAT[A/G]TTGAGGTGATGAGGA	10391
rs557304438	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709632	CGGCTAATTTTTGTT[C/T]CTTTGGTAGAGGCAC	10391
rs557319665	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576069	GAGGTGGGAGAATCG[C/T]TTGAACCCGAGAGGC	10391
rs557321981	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68690737	TTATTGCAGCCTAGG[C/T]CTCCTGGGCTCAAGC	10391
rs557335858	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68624569	ATGTATTAGTTGTGC[A/G]TTCAAATCACCTTGG	10391
rs557342702	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595963	AGAGGCCAGGGCAGC[A/G]ACGCCGTGGGGTGCT	10391
rs557406063	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68659520	GAGTTCGAGACCAGC[C/T]CAGGCAACACAGTAA	10391
rs557415154	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68717254	GGGAGGCAGAGGTTG[C/T]GGTGAGCTAAGATCA	10391
rs557424728	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698317	TCTTGATGTAGGGGG[G/T]ACAAATTAGACCAGG	10391
rs557452568	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68569777	TGAGAGTTCCTGTGG[C/G]TCCACATCTTCCCCA	10391
rs557478509	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68591129	GCAGGGATGTTGGGG[A/T]AGGGAGGCTGATGGG	10391
rs557501083	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641264	CACCCCGAGCCTGAG[C/T]GCTGTGGTCCCCCAG	10391
rs557505693	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68625302	GGGTTCTTCGAGGTA[C/T]AATTTACATGCATTA	10391
rs557508576	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68705151	ATTCAATGTCAAAGC[A/G]GAAAAGTTTGGAAGA	10391
rs557516301	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68658704	TCATTCCTAAGACCT[A/G]CTCTTTGGGATTGGA	10391
rs557522814	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68566948	CGAAGAGGCAGCGTG[C/T]CCAATAAATGACTCA	10391
rs557523897	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68666375	TTTAGGACATAAGGT[A/G]GGTAGGGTGATTCTC	10391
rs557529538	in-del	-/TT	0.307671	0.243257	intron-variant	CORO2B	GRCh38.p7	15:68709460	GATTTTTTTTTCGTG[-/TT]TTTTTTTTTTTTTTT	10391
rs557538015	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68672959	GTACCAGGGTGTGGG[C/G]TATGGGTTGAAGATG	10391
rs557548758	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68706918	GGGTCTCACTGTGTT[A/G]CCCAGGTTGGTCTTG	10391
rs557572199	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560537	CTCCTGGCCTCAAGT[G/T]ATCTTCCTGCCTCCG	10391
rs557578970	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68685052	ATCTTTCATACTGAG[G/T]CTTGGGATTCCAGCA	10391
rs557591604	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68710612	TGCCCATCGCCTCAA[A/G]CCAGGAGGTGGCTCA	10391
rs557616378	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68584933	TGTGGGCCTGGAGTG[C/T]GGGACCAGCTGCTAA	10391
rs557640433	in-del	-/C	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68683707	CCATCTCAGGACACA[-/C]CTGCCTCACCTCCCT	10391
rs557647124	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68573857	GCTCAGGGAGTTGTG[G/T]AAAGCAGCACAGAGG	10391
rs557653170	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68586819	TTCAGTTGCCTACCC[C/T]GATGCCTCACGGAGC	10391
rs557654797	snp	A/C/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727304	GTGGCCCAAGGTCAC[A/C/G]CAACTCTGAGATGCC	10391
rs557692611	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604668	CCCCAATTCCTCATC[C/T]CAGCATTCCAACAAT	10391
rs557727159	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636720	CTAAGTCCCTGTACA[A/C]CCCACCCAGGAACTT	10391
rs557727957	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68643018	CACCAACCACCCATA[C/T]TGTATTTTTCATACT	10391
rs557742859	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643696	GGATTCTGAACTTCT[C/T]CCTTCAATAAAGAGG	10391
rs557746229	snp	A/T	0.0573587	0.15934	intron-variant	CORO2B	GRCh38.p7	15:68708691	CTTCCTTTTTTTTTT[A/T]TTTTCTGAGACAGAG	10391
rs557756169	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651111	GGAGGGTGAGGCAGC[C/T]CCTTGATCTGCGAGG	10391
rs557757847	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727687	GTCAGCACTCATCTC[C/G]TCCTCCCACATTTCT	10391
rs557770034	in-del	-/TAAAG			intron-variant	CORO2B	GRCh38.p7	15:68605235	ATTATCAAAGACACA[-/TAAAG]TAAAGTGGGATCACC	10391
rs557787290	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68557659	CAGACACTGTGCTAA[A/G]CACTTTATATGTAAC	10391
rs557792133	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68589093	GTTATTATGGATTGA[A/G]GCTGTTTCAGGGCTT	10391
rs557799096	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68609845	ACTGACTGTGATGGC[A/C]GGCAGGGTGGGCTGG	10391
rs557807839	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642842	GCTGCACAGAGAAGA[C/T]ATTCCAGGCTAGAAT	10391
rs557866690	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651989	ACTCTCAAGTTCCAG[A/C]AAACTCTATGTTCAT	10391
rs557879252	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68658263	ACCAGGGAGAGGGAA[C/G]AGCTGGGGCCAGGCT	10391
rs557882937	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611175	AAGAAGAATGCAGAG[A/T]CTGGAGTAACACGCT	10391
rs557902844	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717201	CCCCTGTAATCCCAG[A/C]TACTTGGGAGGCTAA	10391
rs557940229	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68656113	AGTTTGCACTTCCAG[A/G]TGGCCTTCCTCATGT	10391
rs557951846	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68562591	GGAAATACATATACA[A/C]AAAAATTACTCATTG	10391
rs557966140	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68704697	AAGAGCCGTTCCCCC[A/G]TATCTAATCTGTTTG	10391
rs557978542	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68590214	GGGTACTCAGGAGCC[A/G]CAAACAAAGCTGCCC	10391
rs558004530	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616239	GCCTTCTCATAATAA[C/T]ACCCCTGCCTCTTCC	10391
rs558012502	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702736	TTGGTTAGATGGAAA[C/T]CTTGGAGCCAATGAT	10391
rs558015375	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589653	TTCCAATTCTGTGGG[G/T]TTTTTTCTAGGCTTC	10391
rs558022012	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575212	CAGCCCTCAAACAAT[C/G]GGGAAGAGGAGGGTG	10391
rs558043386	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623121	AGTGAGCCGAGATCA[C/T]GCTACTGCACTCCAG	10391
rs558043508	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615833	AATTTATGTTGTTCA[C/T]AAGCCACTCAGTTTA	10391
rs558049173	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68582121	TACATCCCCTTGCCC[C/G]CTTAACCATGAGGCA	10391
rs558107972	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583245	TCATGTGTCTCTAGG[A/G]CCCCTACAGAGTCAC	10391
rs558118047	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68621050	CCTGCTGATTAACGG[A/G]TGTGTTACTCAGCTT	10391
rs558123511	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68715558	GTGCTCTGCGTCTGC[A/G]CTCCTGATCGCAGAT	10391
rs558129500	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68622570	TCACCACCTCCCAAC[A/C]CAGCAAATCCTATCG	10391
rs558132817	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68658654	GGCAAGTTACTTAAC[A/C]TCCCTGAGCTTCATT	10391
rs558136461	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630467	CTGCTAGGCTTGGGT[A/G]GGGCTCTGTGGTCTC	10391
rs558172192	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561843	AGTGTGCTTGGTGAG[C/T]CTGTGTGCGTAGTTG	10391
rs558209221	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568998	GAAAATAAAAATTTT[A/T]AAAAGCACATAAAAA	10391
rs558214415	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68722273	AAAGGGTCTCAGAGC[A/C]GACAAAACAGATGCC	10391
rs558233499	in-del	-/GTCC	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68712335	GTTTACCTTGGAATA[-/GTCC]AATATTACAAGACCA	10391
rs558251298	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674477	TGTGAGCAAGGTCTC[C/T]AGAACTGACAGGTGG	10391
rs558270306	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68592667	TATTCATTCACTCTA[C/T]AAATATTTGTTTGTG	10391
rs558284105	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583746	CCTGAACCTCCAGAC[A/G]TTCTACATCCCAGCA	10391
rs558326953	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68673257	AAAGAAAGAGGAGGT[C/T]GGGCACAATGGCTCA	10391
rs558340896	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68653745	GTACTGAGGACTGTA[A/G]TAAAATAATATTTTG	10391
rs558366101	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68664596	ATCTTGCAGTGAGCC[A/G]AGATTGTGCCACTGT	10391
rs558366160	snp	A/G	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68672149	TCCCTGAGCAACTTG[A/G]TAATCGGGAGGTGTG	10391
rs558376718	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68678611	CCCAGGAGACAGAGG[C/T]TGCAGTGAGCTGAGA	10391
rs558387252	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68685281	AGGGGTGCAATCTCC[A/G]CTCACTTCAACCTCC	10391
rs558389500	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679765	CAACCAACCTCCACA[C/G]ATGCAGCAGAGAGAA	10391
rs558414388	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722741	GTTAACAAAAAATAT[A/T]TTTTTAAGTTATATT	10391
rs558434841	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671424	TACCTGCCTCAGTTT[C/G]CCATATCAAAATCTG	10391
rs558439206	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68590394	CTTCTGTTCTCTCAG[G/T]TACCCCCATAACTCT	10391
rs558457516	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637993	GTGTACATAGTGATT[A/C]TCTCAGAGGGGAGAA	10391
rs558480478	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577751	AAAAAAAAAAATTGC[A/C]CAATGACCCACAAAG	10391
rs558504932	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626090	TTGTTTGATTCATAT[A/G]TAAATCTTTCTGCAC	10391
rs558521601	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68657540	AAAAAAAAAAAAGGA[A/C]ATACAGTTATCAAAA	10391
rs558561656	snp	C/T	1.8002e-05	0.00300011	intron-variant	CORO2B	GRCh38.p7	15:68718680	GACCCCATGGAGCCA[C/T]ATGTGTGCCTGTTAC	10391
rs558569516	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68673836	AGCGAGACTCCGTCT[A/T]AAAAAAAAAAAAAAA	10391
rs558570655	snp	A/C	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68688529	ATCTGAAAAAAAAAT[A/C]AAAATCTGAAATACT	10391
rs558605276	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604461	CCTAAGAATGCCTTG[C/T]CAGTCCTAAGCAGAA	10391
rs558626923	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68557523	GCCAGTCTATCCAAG[A/G]TCATACATCTGGAAA	10391
rs558704675	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647325	CACATACTTGACTAC[A/G]ATATTTGCAATATAT	10391
rs558734748	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717913	TCTTGGAACATATTC[G/T]GCTGATCACCTCAGG	10391
rs558738077	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660295	TGTCTGGCATTGCTT[C/T]AGAAGCACTCATCTC	10391
rs558745788	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701982	GCACGGTAGCTCACG[C/T]CTGTAATCCCAACAC	10391
rs558751165	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68651386	GATCTGGCAGCGGTG[A/G]AGATGTTGTTCCACA	10391
rs558759206	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591453	ATGGGGAGCTTTGGA[C/T]GCCAAGCCAAGAAGC	10391
rs558781453	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68676977	ACAGGTTTCACTGTG[C/T]TGCCCAGGCTGGTCT	10391
rs558795437	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667931	TCCCGAAAGCCTTGG[A/G]TTTCTTATTTGTAAA	10391
rs558803551	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701339	TTTTGAGAGACGGAG[C/G]CTCGCTCTGTCGCCC	10391
rs558845377	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652389	TGTGCCCAGCAGCCT[A/G]ATTAACCACTGGGGC	10391
rs558869753	snp	C/T	1.66527e-05	0.00288549	intron-variant	CORO2B	GRCh38.p7	15:68725810	CTGCTCTCTCCTGGG[C/T]CCTCCTTGGCCCCCT	10391
rs558879059	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68576150	AGAGTGAGACTACGT[C/T]GCAAAAAAAAAAAAA	10391
rs558879110	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568662	ATTAGCTCATTTACC[A/G]CAGCCTGAGACTTGA	10391
rs558881392	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68714449	GCTTTTTAACATCTA[A/G]GGGAGGTCTTAACAT	10391
rs558890614	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681518	GGTGGTCATCCAAAT[A/C]TTGGGATTGGGGGAG	10391
rs558896196	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68562304	ATCTTGCCCTCACCT[C/T]CCAGGCAAGATTGTA	10391
rs558910432	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68692639	AAACTTTCCTTTTTT[G/T]TTTGTTTTTTTGAAG	10391
rs558910930	snp	G/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68683749	ATGTTCTACCTCTCG[G/T]CAAGAGAGTGTGGCC	10391
rs558913464	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571132	TATCTCTTTAAAGAG[C/T]TGCCCAAGCACATTT	10391
rs558943619	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68629443	CTGGAGTGGTCCTGA[C/T]GCAGTGGAAGAGGTG	10391
rs558946949	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68620850	TGTCAGGCAGGGTTG[A/G]GCGGGGAGCCAGTTT	10391
rs558952201	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641124	CCAGCCACTGTGGAG[A/T]GGCCAGCCCAGGCTT	10391
rs558971082	snp	C/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68672347	ATCAAGTGATCCTCC[C/G]ACCTCAGCCTCCCAA	10391
rs558983405	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700496	GTCCCCCAGGATCCG[C/T]TTCCCCTCCCTGAGC	10391
rs558986000	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68671643	TCCAAGCTCATTCTT[A/G]CAGCTATTGGCAGGA	10391
rs558993689	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68706141	ACCTCTGGCCTCCTC[C/T]CCACCAGCCAGCCTG	10391
rs559027419	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68626832	CCAGGAGGTCTGGTC[A/G]GAGGCTGGGGCCCCA	10391
rs559043852	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68646939	CTGTTGCCTCAGGGA[C/T]GCACTCAGCTCCATC	10391
rs559044324	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68678358	TGAGCCCCCAGAAGG[G/T]TGCCCCAGGCCTGTC	10391
rs559068854	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617349	CTCTTCTGTGTTTTT[C/G]AAGCACTTTTCTGTT	10391
rs559103811	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68710505	CTTAGGTCTGCAGAG[A/T]CTTCCCAGAGAAAAC	10391
rs559106610	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653820	ACCCCATCACTCCCC[C/G]ACAATCAGCACTGAG	10391
rs559137355	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700769	GGTTTCCAAGCCTCG[C/T]GCTCCCAGCCCTTCT	10391
rs559158717	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677906	CAGCCAGCCACAGGC[C/T]CTCTGCAGCCATGGA	10391
rs559180012	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68584021	CATTTAGCCAGCACC[C/T]TCTGAGCACCTACTC	10391
rs559199230	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706537	TTCTTGATGGCCAGG[A/G]GCAACTATTCTACCT	10391
rs559217104	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577955	CAGGAAGCCAGCACT[C/T]CCGGGCTTGCCAGGC	10391
rs559247784	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68620429	AATTATGAAGTTTGG[A/C]AAACACTGATTCCAT	10391
rs559248763	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582718	AGGCCCTTGCAACCC[G/T]CTTTGTACTGCTCAG	10391
rs559249713	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612595	GAGATGGCTGTTCAG[A/C]AGTTGGAGCACAAAG	10391
rs559291653	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589386	GATTTTTCGAATACC[A/G]GGTATAGACATATAA	10391
rs559335188	snp	G/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68619707	TACACATACATATGT[G/T]TACCCATACATATAT	10391
rs559379161	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583405	GGCTGGCACCTCGGT[C/T]CTGACTCATGGTCAG	10391
rs559379351	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68686317	CTGGGATTACAGGAG[G/T]GAGCCACCACGCCCG	10391
rs559400227	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582094	TGTTTTCCATTTTCC[A/G]CCTCTCTTTCATACA	10391
rs559419162	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68643009	TGCCAGGTCCACCAA[C/T]CACCCATACTGTATT	10391
rs559434092	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68660320	CATCTCCATCAAGTT[A/G]TCTTCTGTTCATTCC	10391
rs559455526	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597691	AAATCCTCCATTGCT[A/G]TGGAGCTCAGAGGCT	10391
rs559462588	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624147	AAGCCAGCTGCCCAG[C/T]TTAAGTCAGGTAATC	10391
rs559483602	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68699019	GCTGGACTTTGGAGA[A/G]GCAGGACATTGACAG	10391
rs559493908	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637549	CCAGGTCAGTTGATA[C/T]CCACATATCACAGAA	10391
rs559515481	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68575193	GAAGGTAATGCCCTC[A/G]GGTCAGCCCTCAAAC	10391
rs559516386	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643862	GGCCAACATGGTGAA[A/C]TCTGTCTCTACTAAA	10391
rs559567996	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68602769	GTGCAATGTGCAACA[C/T]CCACTTTCTTCCTGA	10391
rs559590465	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68721840	ATAACCTCAATCTCC[A/G]AGGCTCAAGCAATAA	10391
rs559599330	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68685816	TGATAAGTTGATATT[A/G]CTCACTGGGCATTGG	10391
rs559636345	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569247	ACCATCACAGTATCA[C/T]ACAGAGTAGTTTCAC	10391
rs559647836	snp	C/G	0	0	intron-variant	CORO2B	GRCh38.p7	15:68634235	CTTATTGAGCACTTG[C/G]TGTTTGCATGATCTT	10391
rs559665350	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585211	CCCTCTATTTAGGGA[C/T]GGATAAACAGAGTGT	10391
rs559696624	snp	A/C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574496	TGTAGAGTAGCACTC[A/C/G]GTACAGGGCCTGGGC	10391
rs559725637	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646376	ACCCTCCGCCAAATC[A/G]CTCAGGGGGAGGAAG	10391
rs559786522	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653552	ACCATACAGGGGCTG[C/T]CCACACTGAAAGGGG	10391
rs559794630	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68686475	TCACTTCCCAGACAA[A/G]TCACCTTGGGCAAGT	10391
rs559800983	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693429	ATCTGAAGGAGACAG[C/T]GGTATAACCTCCTAG	10391
rs559844547	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727338	TTTCATTTGATCTTG[C/T]ACACATTTTCTTTTA	10391
rs559898678	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68619872	GACAATGCTGGCATC[A/G]TCACTCTCATTTTAT	10391
rs559899312	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653960	AATCCATTTTTCAGA[C/T]CTTTCCTCAATCGTT	10391
rs559923307	in-del	-/A	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68627051	CTTAGCAAGGTACTT[-/A]ACCTTTTTTCTGCCT	10391
rs559926495	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68561992	CTGTCCCCCCACTGG[C/T]CTTGTCCCTTCTCTA	10391
rs559945503	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68669011	TGAACCTGGGAGGCA[A/G]AGGTTGCGGTGAGCC	10391
rs559950332	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613482	TATGTGGCAAAGCTT[G/T]AAGGACCAGTCTTCA	10391
rs559957428	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68611421	TTCCCCTATGACTGT[A/C]TATGACAATTTCCTA	10391
rs559960161	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68611427	TATGACTGTATATGA[C/T]AATTTCCTACCTTTT	10391
rs559962420	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660567	GTAGAGATGGGGTTT[C/T]ACCATGTTGTCCAGG	10391
rs559981915	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68619065	TCAGCAGCCCCAGAT[A/G]CAATTACATCATATT	10391
rs559985229	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652596	CCCAGCCATTCTCAG[C/T]CCCAGCTGTACACCG	10391
rs559997668	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652106	CAAGCCAGCTCACTT[A/G]TTTCTGAATCCATGA	10391
rs560007825	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68666382	CATAAGGTGGGTAGG[G/T]TGATTCTCAGATGAG	10391
rs560030926	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68706671	TACTCAAGTGCAGAC[A/G]AGGGTAGCCGGTAGA	10391
rs560043981	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718474	CCAATTCTAAAGCAC[A/G]CACTGTGGTGAGGCA	10391
rs560125905	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68686708	GTTCAAGACCAGCCT[A/G]ATCGACATGGTGAAA	10391
rs560152267	snp	C/T	0.0248432	0.108648	intron-variant	CORO2B	GRCh38.p7	15:68605966	CCTGAACTTGTGATT[C/T]GCCCACCTTGACCTC	10391
rs560158600	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694591	CTCGTGTAAGAGTAT[A/G]TAGGTGGACCCAGAG	10391
rs560171599	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585496	TGAGGCTTAGTGAGA[A/G]TAGGTGAACGGCTCA	10391
rs560210355	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563212	GTAGAGACTGGCCAG[A/G]CACCATGGCTCACAC	10391
rs560213784	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68599215	GACCTCCTCCACAGA[A/G]CCTTCTCTGATCTCT	10391
rs560233315	snp	A/C/T	3.30083e-05	0.00406242	missense	CORO2B	GRCh38.p7	15:68711651	GCCTGCTCACCACCA[A/C/T]GTGCAAGGACAAGAA	10391
rs560246810	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706241	GCATTTTTCTGCCTC[C/T]TCACCGCTTCCAACA	10391
rs560270072	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694062	GCTGGTCTCAAACTC[C/T]TGACGTCAGGTGATC	10391
rs560270082	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68701001	CTGAGGAGCTGGGGG[C/T]GGGATGGACAGGATG	10391
rs560273309	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662091	GTGATTTTCTTAATG[G/T]CTTCTAGGAACTCAT	10391
rs560309494	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68603219	AACACAGTACGTGGT[C/T]GCAGTAGGTGCTTAC	10391
rs560310601	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712296	CCTTCTACACAAGAA[A/G]GGATTAATGCTTGAT	10391
rs560334378	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641235	AACACGCTGAGTGGG[A/G]GAACATGCCTGCTCA	10391
rs560344753	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68667726	ATGGGAGAGTGCACT[A/G]AAGATGGGCGGGGGG	10391
rs560360498	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68579945	TAGGGGCCCACGTTT[A/C]TTGGAGAGACTTCAG	10391
rs560427464	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570122	TCTCTTGCCATATGT[A/G]GATGACTAGGTGGCA	10391
rs560449971	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674190	CCGCCCTCTGCTGGT[A/G]GAATGCTGGTAGCAC	10391
rs560460000	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577081	TGGGAAGATGCCTTA[A/G]GAAGGGTTTTGCACA	10391
rs560485161	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622074	AGCCACTATTTGACC[G/T]TCTGAGTCTTGGTTT	10391
rs560507723	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701707	GCCAGGACGATCTCA[A/G]TCTCCTGACCTCGTG	10391
rs560508391	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68670221	GCTTTGTTGCCCAGG[C/T]TGGAGTGCAGTGGCG	10391
rs560551023	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68605967	CTGAACTTGTGATTC[G/T]CCCACCTTGACCTCC	10391
rs560583627	snp	A/C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661536	CCTTCAAGACTTGGG[A/C/T]GTTAGCAGCTTTACA	10391
rs560614841	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713498	AGAAATGTATTCTCT[C/T]ACCATTCCAGAGGCC	10391
rs560617981	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68659224	TATGTACATACTTAA[A/G]CCTGGAAGAGTGTGA	10391
rs560618791	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68707369	AACTATAAAAAATAT[A/G]AAACACTTCTAGCCA	10391
rs560626040	snp	A/C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568054	GAAATATTGGCTATG[A/C/T]TCATCATTTGTTATT	10391
rs560629679	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68719661	CTGAGACATTTTTCT[G/T]TCTGTGACAAATGCC	10391
rs560670922	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708446	GCTCACTGCAAGCTC[C/T]GCCTCCCAGGCTCAC	10391
rs560671787	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615179	CAGGGCTCCTAGGCC[A/G]GCTCAGGATGCACTG	10391
rs560678675	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563151	TAGAAAAAGAAGAGC[A/C]AACTAAACCCAAAGC	10391
rs560700279	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68579313	GCGCCCGGGACCCGC[C/G]GGCGCCTGCATCCCC	10391
rs560729665	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68644901	AAAGTGGGGTGGGCA[C/T]GTGTACCAAAAGCTC	10391
rs560748788	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586619	ACAGATAAGGACACA[A/G]GCACAGAGAAGCTAA	10391
rs560767140	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633816	CATCCCCTGGCTGTA[A/G]TGTAGATAGATTATC	10391
rs560767866	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570689	GTTACACTGAGGGGA[A/T]TAGTCAGTGTATTTC	10391
rs560782470	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68562846	GCCGGGCGTGGTGGC[A/G]GGCGCCGGTAGAACC	10391
rs560791428	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565310	TTCCTTATTTTTCTT[C/T]TTATTTAAAAAAATT	10391
rs560802172	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68603767	CCAACCCTGCTGGAC[A/C]TTGATGTTGGACTTA	10391
rs560834572	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681313	GGGAGCAGGAGTTGG[A/G]GCGTCTCTTGAGGGG	10391
rs560880051	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723584	TCAGCCTCCCGAGTA[A/G]CTGGGATTACAGGCA	10391
rs560889159	snp	A/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68605546	ATGGCAGTGTGGGAA[A/T]ATATTCGTGCTAAGT	10391
rs560889623	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612658	GCAATCTGAGTTCAC[A/T]CCTTGGTCTGCTGAT	10391
rs560914064	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68705604	ACCCTACATCCAACA[C/G]TTCTTGGTGAAAACA	10391
rs560926196	snp	C/T	0.00478085	0.0486577	intron-variant	CORO2B	GRCh38.p7	15:68612072	CACTGCACCCGGCCT[C/T]AACTTTCTACTTTCA	10391
rs560926642	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68696145	GTCCCAGCTACTAGG[A/G]AGGGTGAGGTGGGAG	10391
rs560939288	snp	C/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68616867	CATGGATCTGAGAAG[C/G]CTTGCAGAATTGGAG	10391
rs560951490	snp	C/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68625560	TATGCAGCCTTTGAG[C/G]CTGCTTGTGCACTCC	10391
rs560953846	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578922	TCCCTCCGCCTCCTC[C/T]TTTGTAGCGAGTTCC	10391
rs560968645	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597861	CATTAGGGGGCCACT[A/G]TGGTGGTCCAGGCGA	10391
rs560983806	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68562775	GGGTCAGGAGATCGA[A/G]ACCATCCTGGCTAAC	10391
rs560986910	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68675247	TGGAATTCCCCTTGC[A/G]GCAGCTGCCTCCCAT	10391
rs560989589	snp	C/T			downstream-variant-500B	CORO2B	GRCh38.p7	15:68728243	CGGTGCCTTGAAGTT[C/T]ATCAGGCAGGATTCC	10391
rs560997481	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668055	AGCTCTTGAGACGCC[C/T]GGTGCCACTGAATAC	10391
rs561005959	snp	A/G	0.0528381	0.153711	intron-variant	CORO2B	GRCh38.p7	15:68705450	TCAAAAAAAAAAAAA[A/G]AAAAGAAAGTAAATG	10391
rs561017393	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68591547	ATCCCATTCACACTT[C/T]AGGTGGTCTGTCCCT	10391
rs561018031	snp	C/T	6.60349e-05	0.0057457	synonymous-codon	CORO2B	GRCh38.p7	15:68711622	CCTCTGCATGTCCTT[C/T]AACACGGACGGCAGC	10391
rs561020479	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68570026	TGCAGAGAGAGGCTA[C/T]TGTACTCTGGTGGGT	10391
rs561040246	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68586452	GAGGGAGCAACAGGC[C/T]GGGGATGAATGGGCA	10391
rs561069398	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576351	GGAGGGATCAGAAAC[A/G]TTTTCCTTCTGCCTT	10391
rs561085117	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618962	AATTTATCTAGGAGA[G/T]GATCACAGTGGCATC	10391
rs561114968	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68585762	GGTTGTGTCCTGCTT[A/G]GATTTGCCTGTGGTC	10391
rs561117648	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68679891	CCTCGGAGGTGGTGC[A/G]TCTCCTTCTCTGGCC	10391
rs561135012	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68655630	ATCTCCTAAGGTGTC[C/G]ATGATAACAATGGCT	10391
rs561144802	snp	G/T	1.6522e-05	0.00287414	missense	CORO2B	GRCh38.p7	15:68719509	GTGTTGTGGTCAACG[G/T]AATAGATTTATTAGA	10391
rs561160920	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68584213	TACTGTAAGTGCCTA[A/G]TGAATGCAGGCTCTT	10391
rs561179380	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679036	GCAGAGTGAGGGCCT[A/T]CCCAGAAATATCACC	10391
rs561200949	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68622733	ACTATTCTGAATCCT[C/G]GGGATGCAGCAGAGG	10391
rs561244741	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660794	CAACATCTGGACACC[A/G]TTTTCTCCAGTGGGA	10391
rs561246100	snp	A/C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687526	TCACCATGCCGCCAG[A/C/G]CTTTCCAAGGGAGGG	10391
rs561262685	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68606064	GCTGGGTGGGTGAAG[C/T]CTCGTTTACTGAAAG	10391
rs561277933	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640737	GTGCTAAGGAAATTG[A/C]CGTCCTTTGTAGGAA	10391
rs561306189	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571619	CCTCATATAGGCCAA[G/T]AATTTTTAATTACAT	10391
rs561335658	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720477	TGCCCGTGGCTGAAG[A/G]TCTCTCATGAGGGTA	10391
rs561339653	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646991	AGGAACATGTGGGCT[A/G]GTTCTTACTGAGGCT	10391
rs561360025	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688131	ATATTATTTCTTCAA[C/G/T]AACTGTTTGCTTGAA	10391
rs561397971	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601662	GAACAGCTAGGAAGC[A/G]TGGCTGAGGTCAAGG	10391
rs561459161	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68725331	CCGAAATCATGCCAC[C/T]GCACTACAGCCTGGG	10391
rs561463289	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633153	CTTCTATGGAGCAGA[A/G]CTGTGTGCTGGACAG	10391
rs561497234	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587858	AGCCTGCCTCGCAGG[C/T]CTTCTGTCTTGCCAC	10391
rs561534061	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68610448	CCCAGGCTTGTCTTC[C/G]TCCCTGATCTCCAGA	10391
rs561535091	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68594692	CACTTCCCATGTCTG[C/G]GAGCCAATGAGCAGA	10391
rs561539397	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592451	TAGAGTATTAACTGA[A/G]ATAGGGTATGAGAGA	10391
rs561547332	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68641754	TTTTGAGACAGAGTT[C/T]GGCACTGTCGCCCAG	10391
rs561565620	snp	C/T	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68607938	GGGCCTTTATCATCT[C/T]CTTGTCAAAATCACA	10391
rs561627146	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694004	CCATGCCTGCTTAAT[A/T]TTTGTATTTTTAGTA	10391
rs561630033	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572338	GCTGGAGCTGTTTCA[C/T]GTTACCTGCCGCTTG	10391
rs561693070	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635092	TGACCTGGGGCTCGC[A/G]CTCCAAGGATCTGTT	10391
rs561739209	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650628	AAACAAAAACTATCT[A/G]TTTACCTATCTGGAA	10391
rs561785479	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68685700	AATCCGGGAAACCCA[G/T]TAAAAATACCAATGC	10391
rs561794847	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68648533	CGGGCGCCTGTAGTC[C/T]CAGCTACTTGGGAGG	10391
rs561795521	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614328	CAAAAGGAAGGTGCC[A/G]TATTATCACATAAAA	10391
rs561801472	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68661480	GTTCTGGTTATCCAG[A/G]CCTTCTTGTACAAAG	10391
rs561824799	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558540	TCACCATTCCCCCAG[C/G]TAACTTATTATTTTT	10391
rs561840963	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559328	CAGCCTTCAGAGAGT[C/T]TGGGACTCTCTCATT	10391
rs561850978	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641277	AGCGCTGTGGTCCCC[C/T]AGGATGCAGCATCCA	10391
rs561867589	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654734	CCTGGCCCATAGTAC[A/G]TGCTAGTAAACGGGA	10391
rs561885802	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68571234	GTTCTGTACTCAGTA[C/G]TCAATATTCAGTACT	10391
rs561996551	snp	A/C	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68594594	TGTTTGTTTCTGTCT[A/C]CTGAAATATTTATGC	10391
rs562003655	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609577	CCACATCTCTTTTGG[A/G]GTTGGGGGAGTAAAT	10391
rs562014795	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629121	CTGGGGAGTGCCGAA[A/T]GTATCTTGCAGTTTT	10391
rs562026298	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68714323	ATAGCAAGTAGCAGG[C/T]TTGGGGACAATGAGA	10391
rs562037656	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68707721	AGGTGGGTGTCTAGC[A/C]CAAGCATTAGTCTCC	10391
rs562052477	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68700326	GTCTGGACCAGTTCC[C/G]CTGGTAGTGCCTGCC	10391
rs562058175	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566450	AACTCCACTTAAAAT[C/T]GGGTCTCTGAGCCTG	10391
rs562064776	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613810	TATAGATGGCTGAAA[C/T]TCCTGAAAGTCTTAG	10391
rs562072553	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560873	AGAGGAAGCAGAACC[A/G]CAGCTCTCCTCACGA	10391
rs562085507	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616004	CTACTGTGCGCCAGA[C/T]CTGCTGGGTGGTTTA	10391
rs562094442	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641255	ATGCCTGCTCACCCC[A/G]AGCCTGAGCGCTGTG	10391
rs562096044	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68708544	TTTTTTGTATTTTTT[C/T]AGTAGAGATGGGTTT	10391
rs562126504	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662893	ACAGACTAGTATCTA[C/T]AGATATTCTATGCAT	10391
rs562140362	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703535	AGTAGCTACTAAGGG[A/G]TTAGATATCAGATCT	10391
rs562157847	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68567313	AGTGAAGTTCAAAGC[A/G]GCCAAAGCAAAAGAT	10391
rs562174041	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616537	CAGCTGCCCTGGATC[C/T]AGATTCAAACCGCCT	10391
rs562205664	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702955	CCTCAGCCTCCCAAG[C/T]AGCTGGGACTACAGG	10391
rs562217443	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618621	TCAATAATCCTATAG[A/G]ACAGGGACTTTTTAG	10391
rs562218223	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574015	GGAAGCCTGGGGGAT[A/G]GGGGCAGGTCTTGGA	10391
rs562245729	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68582871	GTTAGACGCTAGTGA[C/G]CTGAATGCTTTTTAC	10391
rs562248545	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708914	TTGAGCTCCTGGGCT[C/T]ACGTGATCCTCCTGC	10391
rs562266731	snp	G/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727094	GGGGAAGGCAGACCA[G/T]GGTCTGATGGCTTCT	10391
rs562316268	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707178	TGAGCTACCACGCCT[A/G]TCCTCGGTATTTCTA	10391
rs562318345	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613587	GTTAAGAACCAATGA[C/T]GCACAATGCCATGGA	10391
rs562346252	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68585505	GTGAGAGTAGGTGAA[C/T]GGCTCAAGGTCACAG	10391
rs562361264	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600633	GATACCCTTGTGCCC[A/G]CTATGACCATGGGTG	10391
rs562366850	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669348	TGAAATCCACACGGG[A/C]ATCTTGGCACCTCTG	10391
rs562391647	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68683034	CCCATGCACACAGGA[A/G]AAGTTCTGGTGGGTC	10391
rs562405151	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68620852	TCAGGCAGGGTTGGG[C/T]GGGGAGCCAGTTTCT	10391
rs562413838	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635989	TAATTGAGGAGCAGA[C/G]AAGTAAAGGAGAGAC	10391
rs562435964	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68714225	TCAAGGAACAATGTC[A/G]GCCACACCTGCAAGA	10391
rs562454894	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701555	CAGTGGCGCGATCTC[C/G]ACTCACTGCAAGCTC	10391
rs562497372	snp	A/T	1.66668e-05	0.00288672	missense	CORO2B	GRCh38.p7	15:68725967	GCAACAGCCCCAAGA[A/T]CTGTTAGCTCCCCAG	10391
rs562502247	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558423	ACCAGGCTGGAGTGC[A/G]GTGGCACAATCACAG	10391
rs562504990	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559586	TGCAGGGACCAGACG[A/G]GGAGCAGACGGAACA	10391
rs562531587	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68656238	GATGGAGGGATGTGG[A/G]AGGAAGAAGGGTTGG	10391
rs562545954	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68563105	GAAGAAAGATCTCAA[A/G]TCAATTACCTCACTC	10391
rs562559653	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68599924	ATCATAATGAACTGC[A/G]TCCTTGGAGACTGGC	10391
rs562560888	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688303	AGCATTCTGATGTAT[C/T]TTCTTGTAGATTGGT	10391
rs562593032	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68565717	GCTGGGAGAGGTATT[C/T]GTCTATAGCCCTAAG	10391
rs562607168	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662283	TTTTCCGGAATCATA[G/T]TAGAATCTATAGGTT	10391
rs562612544	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68591353	AAGGGGAAACATGTT[G/T]GGCTTATTCTAGGAG	10391
rs562614312	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68694668	TCCTGATCCAAAGCT[A/G]ACTGTGCCCTGGGGG	10391
rs562627621	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578788	CCGCAGGCCCGAAGG[A/G]GTTAAGGCCGCGGAC	10391
rs562632437	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68563744	AAAAAGATTATAAAT[A/G]AATAAGAACAATTGT	10391
rs562645303	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68606852	ACATGGAAGACATTA[A/C]GGGACCCCTGGAGCT	10391
rs562661173	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68599660	ATTCTAAAGGAGGGA[A/G]TGCACTCTCCACTGC	10391
rs562675113	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660664	GTATGAGCCACTGCA[C/T]CCAGCCAAGATTCAT	10391
rs562689304	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706330	AGGCCCTCCCACCCT[C/T]GTCCCCCTAACAGCT	10391
rs562802120	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68677651	AATAGCTGTCTTTGT[A/C]ATAGGCCTTGGTGAC	10391
rs562826706	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68573265	GAGAAAAGGCAAGAG[A/G]GACAAAGAGAGAAAG	10391
rs562843145	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68622126	ATCTCTTTTGCTTAG[A/G]AGTGAGAATTAAATG	10391
rs562862968	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68566293	ATCCCCATTTGATAG[A/G]AGAGGAAACAGGCCC	10391
rs562896839	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709332	ACCTTGCCAACACTG[A/G]CTCTTTTTATTTTTT	10391
rs562916864	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583286	ATAAAATTTTGGAGC[C/G]GGCAAATCACCCAAC	10391
rs562921644	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669300	GGTGAAGGCGACTTG[A/G]AGCCTTTATCTCTCA	10391
rs562935148	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615160	GAAATGATCCTCCAC[C/T]TCCCAGGGCTCCTAG	10391
rs562955480	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68708469	AGGCTCACACCATTC[G/T]CCTGCCTCAGCAGCC	10391
rs562966882	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622665	CACAAGATTCACCCC[C/G]ACACCCCATTCATTC	10391
rs562982960	snp	A/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68676301	ATCTGTGGGTGAGGG[A/T]CATAGGAGTCATGAT	10391
rs562996479	snp	A/C	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68574725	CAACATAATTAGAGC[A/C]CATAAAGAGACAGAA	10391
rs563019840	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68715011	ACACACACACACTCA[C/T]ATCAGCCCATCCACC	10391
rs563019878	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68707914	ATTGGGGTATTCTGG[A/G]CCCCCTATACATCAC	10391
rs563031541	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68714182	ATCAGACAGAGACCC[C/T]CAGAGGCCGAGCTTG	10391
rs563036894	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589211	TATACCAGCCAGCAG[A/G]TAAAGGCCTAATGTG	10391
rs563044164	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68580845	GTGTCTCTTTTTGTG[C/T]GCGAGCTCATGCAGC	10391
rs563059218	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684068	CAACAGTGTGTAAGG[C/T]GGATTGGAGAGAGAA	10391
rs563072859	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726253	AAGACTACAGACTCC[C/T]TGGGGTTGGCAGGGG	10391
rs563073222	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68588715	AAATCATTTAAACAC[A/C]TTGAGTTTGATTTCA	10391
rs563087183	in-del	-/AAAAAAAAAAAAAA			intron-variant	CORO2B	GRCh38.p7	15:68650393	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]TGGAGACATTCCTGG	10391
rs563097084	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713610	GGGTTGCCGGCTCCC[A/G]TGGCTGGTGGCCACA	10391
rs563108593	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574801	CCATGGATACAGCGC[C/T]AGGAGAGCTACATGC	10391
rs563124316	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627551	AACCACGTGCCTGGG[A/G]CAATAAGGAGAGCCC	10391
rs563152935	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675455	GCAGAGGAGGGGTAT[C/T]CTGTGTCTGGAAAGA	10391
rs563153689	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68715981	CCGTTCCCACCTCTG[C/T]GGGTGATCCTCTTTG	10391
rs563170424	snp	C/G	0.00636936	0.0560724	intron-variant	CORO2B	GRCh38.p7	15:68691135	GAGATCGAGACCATC[C/G]TGGCTAACACGGTGA	10391
rs563170470	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68683387	GCATGGCTCTGTGGC[C/G]GGGGAGGAGAAAGCC	10391
rs563189551	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681883	GAAATCACCCCCAAC[A/C]CCAGTCCTCTTATGC	10391
rs563203457	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593814	AAGGTCCCATTGTGG[A/G]GTGGGAAGGTCAAGG	10391
rs563231343	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690588	TTCAGGTTTTACATT[A/G]TTACAATCATGTAAA	10391
rs563248311	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716873	GGAGACCATCGGAGA[A/G]GGGGGCAGGGGCTAA	10391
rs563253260	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68700097	CCCACGGCCTCCCTG[C/T]CTCCTTCAAAGCACC	10391
rs563260794	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630786	TGTGGTCTGTCTTCT[C/T]ATCATTTTGGCCTTT	10391
rs563267024	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560005	CCTCAGACGGCAATG[A/C]AGATCTGACCAAGTC	10391
rs563267863	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721832	AGCTCACTATAACCT[C/T]AATCTCCGAGGCTCA	10391
rs563294702	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68682520	AAGAGATCACATGGC[C/T]GCAGATTGACATTCT	10391
rs563295221	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68638538	ACTCCTAAAACTCTT[C/T]CTGCTACAGTTTCTT	10391
rs563348304	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68702120	CAGCCCAGGGAAGAA[G/T]GAAAAATCAGGTACG	10391
rs563353150	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595419	ATGACAGTGGGATAC[A/G]CCTTATCGTCAGATA	10391
rs563414197	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68698548	ATGAGCCAAGAGACT[C/G]TGTTCAGTTTTGCAC	10391
rs563449428	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642911	AACACCTCCTTTCTC[A/G]TCTGTGGAAACTGTG	10391
rs563462399	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68649747	TTTTTTTAAGACAAA[A/G]AAGTTAATGAGAAGA	10391
rs563510500	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68650567	TAGTGAGCCGAAATC[A/G]CGCAACTGCACTCCA	10391
rs563512913	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704817	TCCCCAGCAAGGCAG[C/G]CTTGCTGGAGAGAGT	10391
rs563546847	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598157	TTCAGAGAATCGGAT[C/T]CCAGAGGCTGAAGCT	10391
rs563576836	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603421	CAGAGGAGCCTTCGT[A/G]GAGGACAAACTGCAG	10391
rs563591570	in-del	-/C	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68672264	TTTTTGAGACAGAAT[-/C]TCACTCTGTCGCCCA	10391
rs563596278	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697655	AAGATGGTCCATCAG[G/T]CTTCAGCAGCCCAGA	10391
rs563616245	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609538	AATGTCTGAGCTCCA[G/T]GGCAGGGGCCTTCCC	10391
rs563644567	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691944	CACAGCTCTGCTCAG[A/G]GAACACTCCAATGCA	10391
rs563658989	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68644008	CACCATTGCACTCCA[G/T]CCTGGGTGACAGCCC	10391
rs563678842	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68710182	CTCAGGCCCCAACAT[C/G]TGATCAGTCTCTGCC	10391
rs563695362	snp	A/G	1.64846e-05	0.0028709	intron-variant	CORO2B	GRCh38.p7	15:68715193	CTGCCACCTTCCTCA[A/G]CTCCATCTCTCCTGA	10391
rs563699030	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68685714	ATTAAAAATACCAAT[C/G]CCTGGCTCCTGCCTC	10391
rs563701294	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68721801	CTCCCAGACTGCAGT[G/T]CTGTGGCACGATCAT	10391
rs563704057	snp	G/T	0.00517822	0.0506191	intron-variant	CORO2B	GRCh38.p7	15:68723931	TAAAAGTAGGCCGGG[G/T]TGGTGGCTCACACCT	10391
rs563704624	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698719	AGCCTCGGTTTTGCT[A/C]GTCTCTGAAACAGTA	10391
rs563716101	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68644648	AAACACTAGAGAATC[C/T]GAGGGGATGACAGTG	10391
rs563762800	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721255	CTTAAGGGGGAGATT[A/G]GCAGGTAACTTGATA	10391
rs563790158	in-del	-/TG			intron-variant	CORO2B	GRCh38.p7	15:68658189	GACATTCTGAAACTC[-/TG]TGCTTCTCCTCCCCT	10391
rs563810423	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68567760	GGCACGGTGGCTCAT[A/G]CCTGTAATCCCAGCA	10391
rs563831155	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652063	TGGGGAAGCTGAGAC[A/G]GCACAGCCGGGCATA	10391
rs563845846	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690507	CTTACTACGCACACA[A/T]ACACACTTTCCTCGC	10391
rs563865911	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68690248	TCAGGGCCTTTTTTT[A/C]TCTGGAGACCCAGTT	10391
rs563873187	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68616635	TACGGCTGTGTCAGC[A/G]CGTGGGCCCCAGCGC	10391
rs563873919	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657618	ACGCCCCATGATTGA[A/G]TGTAGGACACAGTAA	10391
rs563935230	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664764	ATTAACATTTTTATT[A/T]AAAATGAGGTTGAAA	10391
rs563958632	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677082	CCCAGTCCAAGACCT[A/G]TTTTTGCAGCACTTT	10391
rs563969929	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689732	GAGAAGATTGCTGAC[A/G]TTTTTTAAAAATTTA	10391
rs563984957	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68635498	TGCAGGGGAGGGGTG[A/G]CAGCACCAGATTCTA	10391
rs563991684	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575279	CTGATCCACGGGTCT[C/T]TGGGGAACTGAGCCT	10391
rs564033294	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68696256	CACTGTCTCAAAAAA[A/C]AAAAAAAAGAGTTCG	10391
rs564062534	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727137	CGTGTGTCTCAGCAC[C/T]GCTATCTCAGCCACT	10391
rs564082146	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68684476	CACAGGAGAGGAGCT[C/T]GTATGGCACGTACAT	10391
rs564105823	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68566124	GTTGGGGAGAAAGAG[A/G]ATCCTTTCTAAGCAC	10391
rs564151151	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559359	CCCGGAGAATTAAAA[A/G]CCTCCGAGACATCCA	10391
rs564151560	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68643134	TATATTTTTTCTAAA[A/G]CAATTTAAAATAAAC	10391
rs564179570	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608610	GTTGGAGAATGATGA[C/G]AGACCTGTGGGTCAG	10391
rs564181993	in-del	-/TATAT	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68665466	GGCTCTTCTAGCTTA[-/TATAT]TATATTTTAATATAT	10391
rs564196906	snp	A/C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68587923	TGGTCCAGAGCATGG[A/C/G]ACCTGGAGGCAGAAG	10391
rs564199564	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655424	CCAATCCCAGTCTTA[C/T]ATTGACACAATGCCA	10391
rs564224406	snp	A/G	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68682630	TGCCTGTTATAGATA[A/G]AGAAACCCCAGGAGG	10391
rs564270387	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68641773	ACTGTCGCCCAGGTG[A/G]TAGTGCAGTGGTGCG	10391
rs564284382	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68648636	GCCTGGGCCACAGAG[C/T]GAGACTCCGTCTCAA	10391
rs564301721	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726459	CTCTTTCGTCCCACC[C/T]CCTCTTCCCTCAGCA	10391
rs564319953	snp	A/C	0.00438332	0.0466095	utr-variant-5-prime, intron-variant	CORO2B	GRCh38.p7	15:68616590	GCAAGTCTTCCAGGC[A/C]GCGGTCGAATGATTC	10391
rs564343218	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68642140	CGTCTGGGTTCAAGC[A/G]ATTCTCCTGCTTCAG	10391
rs564408456	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616122	TGGTTAAGTAATTGC[C/G]CAAGGACTGACTCTA	10391
rs564408496	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623406	GTGGGAGCCCTGGCA[A/G]TGTCCATGCATGTGG	10391
rs564413715	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614989	TTACCAGGCACTGGG[A/T]TGTGAGAGGGTGGGA	10391
rs564445776	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622919	ATAGATACTTAGCAC[A/G]TGTCTGGTGCTTTGT	10391
rs564455290	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68669692	GGGTTTTGGGCTCAA[C/T]AAAGAAACCCCTGAC	10391
rs564461886	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68610139	GAACGATGCAGAGAT[C/G]TCGGGGAAATGGGCC	10391
rs564486999	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68596204	AGCATGCACTGTGCC[C/T]GTGACCCTAGGTGAT	10391
rs564489431	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68715924	GCAATTCTATATTTC[A/G]GGTCCAAATCACCCA	10391
rs564498926	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561354	CAGCTCACTCTCCCC[A/G]GTCCAGATGGTCACC	10391
rs564504795	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68705533	GATAAAGCAAGGCAC[C/T]TCTCTCCCTCTCTGT	10391
rs564505577	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691920	GCTGGGTGCCAAACA[C/T]TTAATGCACACAGCT	10391
rs564506896	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656870	TCAGTGAGGTGTTAC[A/G]TAAAGCCTGGAAGGT	10391
rs564515760	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651389	CTGGCAGCGGTGGAG[A/C]TGTTGTTCCACACTA	10391
rs564520220	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604060	ATTCTTACCCCATAG[A/G]AGCGTTGTGAGCACT	10391
rs564521254	in-del	-/A	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68670788	TGAAAATAAGCAGAT[-/A]AAAATATTATAATAT	10391
rs564529835	in-del	-/C	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68650858	GGCCAGAGAGGGGCT[-/C]CAGTGCAGGGTGTGC	10391
rs564566000	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698674	CATTTACCATCTGGG[C/T]GGCCAATGGAGTGTT	10391
rs564578882	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657592	AATAAGTGCTTTTCT[A/G]TCAATGCATTACGCC	10391
rs564587539	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68567273	TTGTATTAGTTTTAC[A/T]TGTACATGGGGATCT	10391
rs564600392	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574204	TGAGCTAGGGCAGTC[A/G]CTGTGCTGACAGAGA	10391
rs564613660	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704103	ATATTAGCTGGTCAT[A/G]GTGGTGCGCATCTGT	10391
rs564649785	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68565046	TATTTGTTGCTTCAT[A/G]TGAAAGTAACTTTTC	10391
rs564699767	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699525	GGAGGGGCTGGCCTG[G/T]GCTGCTGATCCAGAG	10391
rs564709597	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566560	CAGGATACCCGGCGG[A/T]CTCTTCATGGTCCCA	10391
rs564717301	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68672444	GCACCACCATGCCTG[A/G]CTAATTTTTGTGTGT	10391
rs564738446	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68585815	TAAATGATTCGGGGA[A/G]GGGTGCTGGGGGAGG	10391
rs564766443	snp	A/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68576856	TGCTAAGCTCCTACT[A/G]TGTGCCCAGGGGTAC	10391
rs564771907	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591626	TATGTGCAATGAGGC[A/G]GGGAAGGGGTTTCTG	10391
rs564777552	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68582554	TCTGTTCCATCTCAG[A/T]CATGTACCAGACTAG	10391
rs564781396	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68588036	AAGTTAGTAGTCTAT[A/C]TCTGTAGGGTGCTCT	10391
rs564822712	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677669	AGGCCTTGGTGACTT[C/T]GTGTTGGGAAATTGT	10391
rs564854602	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618858	GTTCAAGGGGATGTT[C/T]GAATACAAGCCTGAA	10391
rs564854934	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611474	CATGGCATCAGGAGC[A/G]TTTCCCCATTGTATT	10391
rs564857305	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713482	GGTGGCTGAAAACAA[C/T]AGAAATGTATTCTCT	10391
rs564882732	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68658948	ACACGCCTTTGCCCC[A/G]GCTGTTTCTCCCTCT	10391
rs564898888	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586086	CACATGGCAGTCTGT[C/T]ATTTACTTGCTGTGT	10391
rs564906298	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575476	AGTAGCTGGGATTAC[A/G]GGTGCCCACCACCGC	10391
rs564919018	snp	A/G	0.00755907	0.0610114	intron-variant	CORO2B	GRCh38.p7	15:68691725	CTTGTCTCCTTCCCG[A/G]GTGCAGGGCTCTGGC	10391
rs564920528	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624270	TGCAGTCCCAGCTGC[C/T]CGGGAGGCTGAGGCA	10391
rs564928720	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648607	GTGAGCCAAGATTGC[A/G]CCAGTGCACTCCAGC	10391
rs564936246	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618080	TCAGACTTTTTTGCT[A/G]TAGTTGCTAGTGAGA	10391
rs564938550	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68585615	CTTTGGTCCTGGGGC[A/G]TGATCGTACTCTGCT	10391
rs564959674	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630981	AGCCCCCTAGTGGAC[C/T]TCCTCCTAGGTCTCA	10391
rs564964141	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68622264	TGGAGTGTGTGGGGG[C/T]ATGGGCATGTTTTGA	10391
rs564979403	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576222	CAGTATCTCCTACAT[A/G]CAGAGGCCGTGACTG	10391
rs564996824	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68622286	ATGTTTTGAGACTGC[C/T]CAGCTGGGTGGACTG	10391
rs565022764	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711116	TTCTCTGGTGGTTGA[C/T]TGGAGGAGAATGCCC	10391
rs565029028	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717457	AGGAAGACGGGGAGA[A/G]CAGTGTGAATCCAGA	10391
rs565051262	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684894	AATACCTGTTTTATA[A/G]TGACTCTCTCTCTTT	10391
rs565055119	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687395	GCTGCAATGCAGGTT[C/G]GTTTGAAACTGTCTC	10391
rs565063915	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68722539	ATTGTAAGCTTAAAA[G/T]GAGTGACTTTTATGG	10391
rs565065195	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591752	CTGGACCACTCCATG[G/T]TATGGGCCTTTCCCA	10391
rs565066596	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68584152	TTGAGTTCAGAGTCT[C/T]GAGGTCCAGTGGGCA	10391
rs565095565	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716944	GATAAGGAAATCATT[A/T]TGGGGAGGGTTCTTT	10391
rs565124994	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658739	GGTGTAAATGAAACA[A/G]AGTAGATAAAGTACC	10391
rs565129741	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678935	ACCGCTGTACTCAGG[G/T]TGTGTTCCCCTCCCT	10391
rs565144036	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68644235	GTAGTGACTCAGCAA[C/T]CCAGATTGCTTTAAT	10391
rs565155631	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725227	TACAAAAATTATCCA[A/G]GCATGGTGGCACATG	10391
rs565156550	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681070	ATACAAAAATTAGCC[A/G]GGCATGATGGCAGGT	10391
rs565165025	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68686667	ACTTTGGGAGGTTGA[A/G]GCGGGTGGATCACCT	10391
rs565166020	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68597538	CCATTGTGCCCCAGG[A/G]CCCATGCTGTTAACT	10391
rs565166125	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589939	GCCCTACATGCCTGG[C/T]TGCCCCCCTGGCCTC	10391
rs565169747	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68693938	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGTCTCA	10391
rs565193271	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675827	CACCTTCTCTGTACC[C/G/T]GGCACTGTGGGAAGC	10391
rs565203795	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68596858	GCACTCCCCACGCCC[C/T]TTCCCACAGGCCACC	10391
rs565234030	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68693557	GCAGGAAAAAGACCT[C/G]AGAGATGGAAGCATA	10391
rs565251429	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68680088	CTCTTGGTGGATGGC[G/T]GTTCTCTCGGTGGCT	10391
rs565252054	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68562693	GAGACAATGAAAACA[A/G]GCCAGGCACGGTGGC	10391
rs565255120	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578036	CCACCCTCTCCGCGG[C/T]TCTGTATCTGCGGAA	10391
rs565301575	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718493	TGTGGTGAGGCAGGT[A/C]TGGCCCAAGGAGCTT	10391
rs565307431	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632969	ACTAACATTATTTTT[A/T]AAATTACAGTGATCC	10391
rs565323798	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674294	TCTGAGAGCTCCCTG[C/T]TGGGGGCTTCGGGAC	10391
rs565333125	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68723746	GTGAGCCACCGTGCC[C/T]GGCCGATACCTTCTT	10391
rs565347496	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68653309	ACCAAGTCTTGACCA[C/T]CTAGAGTTTGTAGTC	10391
rs565348149	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625525	TTTTTCCAGAATATT[A/G]TATCAATGGAATCAT	10391
rs565380391	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68567940	CAGAGTATTGCTTGA[A/G]CCCAGGAGGCGGAGG	10391
rs565381814	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68598345	TGTGTGCACGTAAGC[A/G]TGTGCTTTGGTAGGG	10391
rs565413052	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724685	CAACTCTCTTTTTGT[G/T]CTCATTTCATCAATT	10391
rs565478599	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639790	AGAGTTCAAAACCAA[C/T]CTTGAAAACCAATCT	10391
rs565483266	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604843	TTTTGAGGCTGGGCA[C/T]GGTGGCTCACGCCTG	10391
rs565488411	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598395	TTCTGCTGTCTCTGC[C/T]TCTCTATTTTGCGTG	10391
rs565489671	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68645444	AGGCCTGTTGACCCT[A/G]CTTCTCTCTGAGTTC	10391
rs565502410	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574310	CTGGGGTGGCATAAG[C/T]GAGGCAGGCAGCAAG	10391
rs565532450	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68628690	TATCACCACAGTTGA[C/T]GGACAAATGGGGCCC	10391
rs565546935	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652663	ACCACAGTAGTGTGG[C/T]CTGAGGAGCTTTTGA	10391
rs565575302	in-del	-/A	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68661554	AGCAGCTTTACAGAT[-/A]AAGGGTAGTCCTGAT	10391
rs565579981	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700040	TGGAGTTTGCAGCTT[C/G]CAGGGGGTGGACAGG	10391
rs565598378	snp	A/G	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630081	TGCCCACCAGGCACC[A/G]TGCCAGATGTTCTGC	10391
rs565620420	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612050	TGCAGAGGCTATAGG[C/T]AGGAGCCACTGCACC	10391
rs565623118	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68675539	GCCACTTAGTTGCTG[C/T]GTGATCTTGAGCAAG	10391
rs565628789	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68581359	CCCTTCACAGACCAG[C/T]GTGTTCTTGTGGGGA	10391
rs565632992	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677229	AAGCTCCCAATTGAA[C/T]CCCAAGCCCCATCAC	10391
rs565641787	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616224	AGAATTATCACTGGA[G/T]CCTTCTCATAATAAT	10391
rs565662332	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68663211	GGAGATCTTTTCACA[C/T]CAAATATAGAAAGAG	10391
rs565663188	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650970	ATCAGCCCTCCCTTA[C/T]GTATGTTGCAAATGT	10391
rs565696325	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708657	GTGAGCCACCGTGCC[C/T]GGCCCTGCCTTTGGC	10391
rs565701287	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630080	GTGCCCACCAGGCAC[C/T]GTGCCAGATGTTCTG	10391
rs565715131	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68659665	TCGGCCAGACATGGT[G/T]GCTCATTCCTGTAAT	10391
rs565721578	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68684526	TGCACATGCAAGCAT[A/G]TACATGTGTATGTTG	10391
rs565724047	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68626727	TCCATTTCGTTGGCT[C/G]GGGAGAGACCCAGGT	10391
rs565726000	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664331	AAAGTGTAAGTGTGC[C/G]TGTTCATTTAACCTC	10391
rs565727716	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617630	GGACCAGATAAACTC[C/T]AGGTCTTTCCTTGCT	10391
rs565729676	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625128	TTGCAATGGGCGGTC[C/T]GAGCATGCCGCTGTA	10391
rs565759123	snp	A/G	1.67136e-05	0.00289076	intron-variant	CORO2B	GRCh38.p7	15:68715360	CTCATGGCACGGGAG[A/G]ACATCTGGCCCATGG	10391
rs565760097	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717542	GAGAGGAAAGAAGCA[A/G]GAAGGGCTCAGAATG	10391
rs565790523	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68587209	CTAAAACAAACAAAC[-/A]AAAAAAAACCCCCTA	10391
rs565796481	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709451	TTTCGAAAAGATTTT[C/T]TTTTCGTGTTTTTTT	10391
rs565797429	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68655208	GCTCAACAAATCTGA[A/G]CTATATTTCTTCTAT	10391
rs565870232	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588106	TGTAGATGTCATGGC[A/T]GGAAATGGTTTATTG	10391
rs565871048	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723215	CAACCTCCACCTCCC[A/G]GGTTCAAGCAATTCT	10391
rs565875266	snp	C/G/T			intron-variant	CORO2B	GRCh38.p7	15:68683569	TTTGGTGCACCACCC[C/G/T]TCCCCCCACTGTAGG	10391
rs565912529	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68629612	CGATGTGCAGGGAAA[A/G]GCTATGCACTGAGCA	10391
rs565933166	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68722682	CAAAGGCAAATAGCA[C/T]GTCATCCCTCTCAAC	10391
rs565958796	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597110	TGCAGGGAATTGGTG[G/T]CCTGCTCATTTCAAA	10391
rs565960720	snp	C/T	4.07764e-05	0.00451514	synonymous-codon	CORO2B	GRCh38.p7	15:68710758	GGAGATCCCCGAGGG[C/T]GGGCTGAAGCGGAAC	10391
rs565961731	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68588887	CCTGCCCTGCTGACC[A/T]CCAGGTGAAAGACCA	10391
rs565974149	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68683633	GAGCCTCACCTTCCC[G/T]CTGCAGTATCCCTAC	10391
rs565994026	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68596570	GCTCCCATAAGGCTG[A/G]CCTGTGCTAGCTGCT	10391
rs565996008	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68573627	GTGGTGGGGGACAGC[A/G]GCTGGGTGACAAAAC	10391
rs565998498	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68628808	ACTCACCCAGCCTCT[C/G]CATTCATTCCCTGAG	10391
rs566016116	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68595568	CTTCTCCCAGGGGTG[A/G]GTTCTGTTCTCAGCT	10391
rs566023372	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68711329	AACTGAGCCCAGGCT[G/T]GTGCTGGGATCTGAC	10391
rs566042221	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68568837	CTGCCAGCCAGGAAG[A/G]GGAAGGAGAGCATCA	10391
rs566044489	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576472	AGCCCACAACAACGG[C/T]GGATGGCGGGAAAGG	10391
rs566082957	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575720	CCCCAATCTTCCACT[A/C]CTGTGATCACCTTCC	10391
rs566104631	snp	C/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727746	CCTTTGTGGTCTTCT[C/G]TGATTATTTATGCTG	10391
rs566109989	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68672722	TCCTGTTCTGGGATG[A/G]AGTGGCCTAGGGAGA	10391
rs566151824	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700642	TGGCATCTGGCAGAA[C/T]CCAGTTCTTTCCGCT	10391
rs566166007	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589616	AACTGGGGCTCCCCC[A/G]AGTTACTGCTCAGGT	10391
rs566175092	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679121	CCTGGCACCGTGCTG[A/G]GTGTTGGGATACAGT	10391
rs566180880	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631092	GTGCTGGGAATGGCA[A/G]GTACGAGTCCAGTCA	10391
rs566184167	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637286	ACTGGGAATTACTGC[C/T]CAGGCTGGCGAGCCC	10391
rs566214967	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68728144	GTCAGAATCACCTCC[C/T]GGTTAAGAACCACTG	10391
rs566219555	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637951	TTTTGAGATCCGAGG[A/G]CAGGATACAATTTGC	10391
rs566233960	snp	A/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68685102	GGTTCAGCATGATCC[A/G/T]CTGCCCTCGGTACTC	10391
rs566275171	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722045	GTCATGAGACACTGC[A/G]CCCAGCTATTTTCTT	10391
rs566285094	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644086	CCAACTACAAAGTAT[A/G]TCAGTTACAACAGGC	10391
rs566312872	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687630	TTTAATTTCAAAGAT[A/G]TATTTTCCCTGGTCT	10391
rs566317056	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68645101	CCCCCAAGAGCCCAG[C/G]CGAGGCCCTTCATGG	10391
rs566342925	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68692049	GTCTGCCCATGAAAA[A/G]TCTGAGCTGCAGGAG	10391
rs566346232	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68651587	AAGCTATTAATTCAT[G/T]GTGGGACAGTCTTGT	10391
rs566378199	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652345	GGCACAGCTGGAGGG[A/G]CCTTATGAATATTCC	10391
rs566416599	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632676	GCTCACTGCATCCTC[C/T]ACCTCCCTGGTTTAA	10391
rs566427716	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68609972	CCCTGTAATTGTGCA[A/T]CCAGCCTCTCCCCTC	10391
rs566432935	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680283	GTGTAAGAAGCATGT[C/T]TGTACCACTGAGGTT	10391
rs566445516	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68643222	CCCACTTTGGGAATA[G/T]TTGGTGTCCTGATGA	10391
rs566474496	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68724891	CAGGAGAAATGGAGG[C/T]GGGTTAAGCTAGAGA	10391
rs566474694	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718262	GGCCTCTCCCTCCTT[C/T]CTCTCTCAGGACTGG	10391
rs566475124	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68705699	GCCTGGGCATAGACA[C/T]CAGTTACCCTGACCC	10391
rs566486246	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68724097	ATCCCAGCTACTCCA[A/G]AGGCTGAAGCAGAAG	10391
rs566486695	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605584	GTGGGACATAAAGTT[C/T]TATGCATATCATGAT	10391
rs566498123	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591838	GAGGACCAGAAGTTT[C/T]CTTCTAGGAAAACGT	10391
rs566501865	snp	C/T	0.000149233	0.00863679	missense	CORO2B	GRCh38.p7	15:68725915	GCCCAGAAGGACATC[C/T]GCATTCGGCAGCTCC	10391
rs566512232	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68559643	GACTTTTTCTTTCCC[C/T]AACCCTTTCCCTGTC	10391
rs566578835	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693641	GAACAGCTCTTCCAC[A/G]CCCATCCACGCCCCT	10391
rs566607568	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68620991	ATGCTGCTCCGCTTC[C/T]GGGAAGCTATTACTT	10391
rs566610226	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701302	TCTAGGACTAGTTTC[C/T]TTTTTTTCTTTTTTT	10391
rs566635703	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68605064	GGTTGTGGTGAGCTG[A/G]GATCATGCCACTACA	10391
rs566640838	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693241	TTGCAAAAGATCAAA[C/T]GATCTGGAAATGAGC	10391
rs566642514	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700129	GAGGCATCGGCCACC[A/G]AGGCCCTCCCTCCAC	10391
rs566644450	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68668203	CACACAGTGAGCCTC[A/G]GTCAGCGAGAGGGCC	10391
rs566687327	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571054	GGAGGGAATGGATGA[C/T]TGACATCTAAAAGCC	10391
rs566698288	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68562209	TGGGTGCTGAGCACT[A/G]GGTTGACTATGGGGT	10391
rs566725626	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68611705	ATAATAGTTTATTTT[A/G]TGAACATAAACATAT	10391
rs566748580	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569662	AAACTCCAGGGAGAA[C/T]GATTGCTGGATCATA	10391
rs566777670	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68619971	GGCTGGAGTACAGTG[A/G]CACAGTCTTGACTCA	10391
rs566789911	in-del	-/T	0.415563	0.18732	intron-variant	CORO2B	GRCh38.p7	15:68602009	ACACGATGGGAAGGC[-/T]TTTTTTTTTTTTTTT	10391
rs566792366	snp	C/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68638328	TAGAGCTAGTGTTGA[C/G]CAAGCACCCATCCTG	10391
rs566804319	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705198	AAATGTGCAGATGAA[A/G]GCCAGGTACAGTGGA	10391
rs566812915	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68660915	GTTCTCTCTATAGAG[G/T]TTCTCTTTCTTAGTG	10391
rs566814634	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68579471	GGCCAGGGGGAGGAT[A/G]CCGCTCTGGCAGCCC	10391
rs566819577	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674428	CCAGGTGATTGTGTG[A/C]CCTGGGTCTTCAGGT	10391
rs566831873	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68673793	AGTGAGCCGAGATGG[C/T]GCCACTGCACTCCAG	10391
rs566895995	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68686009	ACTAGAAATGTTGAG[C/T]TCCTACTTCTGTTTT	10391
rs566908932	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712976	TTTTTGGTGGAGCTA[C/G]AACTAGAGTTCAGAG	10391
rs566916780	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68653796	GTTCCCATTCCAGAT[C/T]TCTGTAACACCCCAT	10391
rs566939005	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68689988	ATTATTATAAATTAC[A/C]TTGAGTAAACTTGCA	10391
rs566951609	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578244	CAGTGGTAGTGTAGA[C/G]AGTCCTAGGGCAGGG	10391
rs566961243	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613157	AGCTTACACCCAGTT[A/G]GCCAACACTTTATCG	10391
rs566976930	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621047	TCGCCTGCTGATTAA[C/T]GGGTGTGTTACTCAG	10391
rs566978915	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68660212	TCTTGAATAATTGGA[C/T]CCTTCTGCCAGATTG	10391
rs566989040	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68666816	TGCACTGAGTCCCCA[A/G]AAATGATAAAAATAC	10391
rs567011160	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68706469	GGCTCATAGGAGGCC[C/G]TCGGGAGGTGTTAGT	10391
rs567046577	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68668383	GTCAGGAGACAAACA[A/G]TGAACAAGGGCGCAA	10391
rs567055061	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68601456	AGGCCTCAGCCTGCA[C/T]GGAGCTTACAGTCAA	10391
rs567059278	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680935	TTAGGGAAAAGGGGC[C/T]GGGCGCGGTGGCTCA	10391
rs567064625	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68620102	TTTTTAGTAGAGACG[G/T]GGTTTCACCATGTTG	10391
rs567067507	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68633289	CTCCTCTTTCCTTGC[G/T]GGGTCCTAAATTAAC	10391
rs567074443	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712690	TCACTGTGTGGCCTG[C/T]ACTGTGCCCGGGGCT	10391
rs567083328	snp	C/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639921	ACCAGGATCTGGGCA[C/G]GGCTTTAAGGGTAAA	10391
rs567103951	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68658456	TAGGCCAGATAACAA[C/T]CTGGGTAGAAGCGGG	10391
rs567115806	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693615	TGCCACCTTTGTAGC[C/T]GCTAAACATGGAACA	10391
rs567191517	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68562088	GAAAGGCCTTAATGA[A/T]GTTGTCCTCCAGCCA	10391
rs567208499	snp	C/T	9.73264e-05	0.00697522	intron-variant	CORO2B	GRCh38.p7	15:68718653	GTGATGTCACTGAGA[C/T]GCAGTTTCTGGGACC	10391
rs567220892	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68621251	GCACAGACAAATCAC[A/G]CACTGCCTCCAGCCC	10391
rs567233725	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68562101	GATGTTGTCCTCCAG[A/C]CACCCCTTCCCATGC	10391
rs567236198	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68675424	AGCCTCTGAGGGCAG[A/G]AATAGCATCTTCTAG	10391
rs567245848	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68639062	AGGGCTCATGAGGGA[C/G]GGTAAGGACCAGACC	10391
rs567259966	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68645057	CCAGGGCCTGCTCAC[C/T]TGCTGCACCTCTGAG	10391
rs567276155	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597939	AGGATGCAGGGTGAC[A/G]TTTTGGAAGTTGATG	10391
rs567277396	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68700716	CTTCTGCCGCAGCTA[A/G]GGAGGGCGGCTGGCA	10391
rs567288272	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639658	ACATCGTCCTTAATC[A/G]GAGGTCATCCACCTA	10391
rs567299222	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68693961	CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	10391
rs567301358	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698991	AAGGTGCAGAGAGGA[A/G]AAGAGGTAGTTAGCT	10391
rs567326482	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68604982	AGCCAGGCATGGTGG[C/T]ACACACCTGTAATCC	10391
rs567331914	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693077	TATCCTCTAATTTTC[C/T]CACAACATACAACAT	10391
rs567335809	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68618127	GACCCAATACACACA[C/T]ATGCATACACACACA	10391
rs567341116	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706432	AGAGCAGGCATGGGC[A/G]AGTTCAACACCACAC	10391
rs567388700	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68666196	GTAGAGAAGAGGCTC[C/G]AACAGATAATTCTTT	10391
rs567395413	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699646	CTTACCCGGGTGTCC[A/G]CCCCTCCCCGCCTTG	10391
rs567403722	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68673198	TGTCAGAGTTGGAAG[C/G]AGCCTCAGAATTGAT	10391
rs567451696	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68705846	CACACACCTCTAACA[A/G]GTACAGTCTCTATTT	10391
rs567482425	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704493	CTCACAGCCAATAAG[A/G]TCAGAGCCTGCATTC	10391
rs567503655	snp	A/C	0	0	intron-variant	CORO2B	GRCh38.p7	15:68563340	AAAAAAAACACAAAA[A/C]TTAGCTGGGCGTATT	10391
rs567526362	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68617432	GTTCTAGTCCCAGTT[A/G]TGCTACTCACCAGCT	10391
rs567526852	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585280	ATGTGGGTCAGAGGC[A/G]GGATGCACGCCCAGA	10391
rs567534049	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613041	CCCTCTCTCACTTCA[C/T]CAAAACTCCTGATGG	10391
rs567537092	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585651	TCCCCACCAACCCCC[C/G/T]ACCTACAACACAGTG	10391
rs567554176	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699310	CATCAGTGGACCCCA[C/T]CGAGTGTGGTGCATG	10391
rs567563637	snp	A/G	5.87492e-05	0.00541952	synonymous-codon	CORO2B	GRCh38.p7	15:68710779	GAAGCGGAACATGAC[A/G]GAGGCGCTCCTGGAG	10391
rs567570776	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68653237	TAACAGATGGGTATT[A/G]AATGCCTGCTAGGTT	10391
rs567572678	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68624052	GACTTAAAGGACTGG[A/G]GTGGCGGGTCCTGCT	10391
rs567591580	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68710657	GAAAGCCTGGTGTCC[A/G]AGGAAAGGGGCACCT	10391
rs567616093	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68696991	CCCAGACTGGACTGT[G/T]AGCTCCTGGGAGCAG	10391
rs567629342	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679440	GTGAGGGTGACAGCC[A/G]TGACAGCCATTAAGC	10391
rs567647518	snp	A/G	0.0150606	0.0854603	intron-variant	CORO2B	GRCh38.p7	15:68604350	ACCGCCTTTCCTACC[A/G]CGAGCAGAACAAGTG	10391
rs567677184	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674356	GCCCGGAAGACAGAC[A/G]AGGCCATCAGAATGC	10391
rs567680681	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68718031	GGGCAGAGTGAGGAC[C/T]CAAACCCCGTTGGTC	10391
rs567685132	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712565	TCCAAAATCTGAAAC[A/G]CTTCTGGGCCCAAGC	10391
rs567749779	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68627338	AAGCAATGCACCAGG[A/G]CAGGGCAACTTGCCC	10391
rs567756106	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68619317	TCACTTAGATTTTCA[A/T]CCTGCTGCAATGTAT	10391
rs567769493	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626644	GGAATCACTGCTTCT[A/G]GAGCAGTGGCTTTTC	10391
rs567770829	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667395	GGGGTATCGTGGTCT[G/T]TTTTCACACCTGTTC	10391
rs567833913	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68634001	TCCTGAGAGTCGGTC[A/G]GGGCATGTCACAGGC	10391
rs567848815	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68718228	GGCTGCGTCCAGACC[A/T]CTAGGGTGTATGGGG	10391
rs567855922	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68625920	CAGCTTTACTGTATT[G/T]GAGAGTCATCCGTGG	10391
rs567892122	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68632445	AGAGACAGAAGTTGA[A/G]AAACGTCCTCTCTCA	10391
rs567892400	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725677	TGAGCTAGAGATGGG[A/G]GAGGTGCAATAAATG	10391
rs567893372	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639815	CAATCTCAAAACCAA[C/T]ATGTCCCAGTCTTGC	10391
rs567899089	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68598472	AAGGGCAGCAGTCCA[A/G]TTTTCTCTAGAGAGT	10391
rs567920823	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723927	AAAATAAAAGTAGGC[C/T]GGGGTGGTGGCTCAC	10391
rs567955438	snp	G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68713742	CACCTGGATAATCCA[G/T]GGTAATCTCATCTCC	10391
rs567979527	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631956	GCCATCCCTCAGCAT[C/T]GCTGGAGTGGGCTCT	10391
rs567982929	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591307	AGGAAAGGCATTCCA[A/G]GTTGAGCGGGCAGCG	10391
rs567998319	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68576223	GTATCTCCTACATGC[-/A]AGAGGCCGTGACTGG	10391
rs568026475	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68580273	GCCTCGGGCTTGGCC[C/G]TCCATTCAAGGGCCA	10391
rs568051624	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68713097	TTAGGAGGAAATCAA[A/G]TGTCACGAGCCAGTG	10391
rs568058810	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68586711	ATTCTGGCCTCTTTC[C/T]TTCCCGCTGCCTGCT	10391
rs568066347	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68579453	GCCCCCAAGGACTGC[A/G]GAGGCCAGGGGGAGG	10391
rs568085772	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68682820	GCTGCTGTAGCAGTG[C/T]TTTAGTAATGCTCCC	10391
rs568112963	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68719289	AGCCTTTGCCTTCAG[C/T]GCAGCTCACCCCAGT	10391
rs568138420	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636397	GGTATAGAATAGACC[A/G]TGTCTCTGGCTGGGC	10391
rs568162904	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68661596	CTACATTTGCACAAA[A/G]CAGTAGAGTTAGCCT	10391
rs568166558	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647218	AGCCAGGAATCCCCC[A/C]AATCATAAAGGAAAT	10391
rs568242697	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694736	CCAGCATCTGAGCGT[A/G]CGTGAACAAGGCAGA	10391
rs568252423	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640414	GGGATACAGGAACAA[C/T]TTTGGCATTGCCCTG	10391
rs568268793	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592666	ATATTCATTCACTCT[A/T]TAAATATTTGTTTGT	10391
rs568285966	snp	A/C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68658611	AGCCCTAGGTCCACC[A/C/T]GAGCTGCTTAATGGC	10391
rs568299460	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68648212	ATGGCATGTGCCTGT[A/G]GTCCCAGCTACTTGG	10391
rs568299493	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655609	CTTCTCAGAGTCCAC[A/G]CTCACATCTCCTAAG	10391
rs568308504	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558095	GGGAGGGTGGGTGCG[A/G]GCAGAGAGGCTTCAG	10391
rs568319600	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635568	TCCAGAGACAAGTCA[C/T]TCCTCCTCTCTGGGT	10391
rs568329302	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68687824	GAGAAGACCAAACTC[A/G]CTTTTATAACAAACC	10391
rs568359355	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655062	TCTAGGGAGGGTCCA[A/G]GGCTGCCATGGAGCC	10391
rs568370381	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642091	GCCCAAGCTGGAGTG[C/T]AGTGGCGCGATCTCG	10391
rs568379554	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68557358	CTGGTGCCAATCTAT[C/T]CAAGGTCATAGCAGA	10391
rs568384406	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68694352	ACAACAATGCTAAAA[A/G]GTAGACATTGCTATT	10391
rs568384850	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595006	CAGTTCTAGCTGTCC[A/G]TGCAGTTCTAGCTAT	10391
rs568414769	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68690759	GGCTCAAGCAATCCT[C/T]CCACCTCAGCCTCCC	10391
rs568417691	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68724127	GAATACCTTGAACCC[A/G]GGAAGCGGAGGTTGC	10391
rs568421799	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68627758	TCTTGCAGGGGTAGC[C/T]TCATCTCCCTCTGTC	10391
rs568422246	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68663500	CACACACACGCAGAA[G/T]AATTTCCTCCTGACA	10391
rs568512527	snp	C/G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68633972	CAGGCACTCTGAACA[C/G/T]GGGATCCCGGTTATC	10391
rs568516120	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559033	TCAGTAAATATGTTC[C/G]GAGATCCTACCACGC	10391
rs568529197	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601834	AATAAAACACCTGAG[C/T]CATTTATAAAGAACA	10391
rs568549314	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633416	AGTACCATTAAGTTT[A/C]ATTTAAAAAAAAAGT	10391
rs568557783	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68559719	GTTCTCCCAGGGGGA[C/T]TGTCGGTGAGGCTGC	10391
rs568580385	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68686193	AGGCATGTGCCACCA[C/T]GCCTGGCTAATTTTG	10391
rs568592888	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565793	CCTTCTGTTCTGGAT[A/G]GAAATAATACCTGCT	10391
rs568603680	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68564840	GCTTCCCAAATAGAA[C/T]GAACAAGTTTTCTGT	10391
rs568605878	snp	A/G			downstream-variant-500B	CORO2B	GRCh38.p7	15:68727983	ATTGACATTTGGGGC[A/G]AATAATTCTTTGCTG	10391
rs568612133	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68696397	CTACTAAAAAGATAA[A/T]AATTAGCCAGGCGTG	10391
rs568618464	snp	A/G	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68608760	TGCCCAGACTCCCGA[A/G]TGCCCTTTCTCAGGC	10391
rs568622642	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615365	CCAGGTCTTGCTCCT[C/T]TCTGTGTAACCCGGG	10391
rs568623705	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68702355	CCACAACGACCACTT[C/T]ATGCATCCTCTAGCA	10391
rs568638560	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640363	TAGTAACCTGAATCA[A/G]ATCAAGGCCTTAGAC	10391
rs568640520	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68706282	TCTTTTTAAACTTAG[C/T]TCAACACCCTCTCTT	10391
rs568657435	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708133	ACCCAAGGGTGACCC[C/T]AAACCCTTGACAGAA	10391
rs568668397	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68621593	CTCTGCCTTTCCAGA[C/T]GGGTTGGTTACCAGA	10391
rs568683601	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68662375	TATTTTGAAAAGTGC[A/G]GGGTTTTCATGCCTG	10391
rs568708722	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68612032	CACCTCCACTGCCCA[A/T]AGTGCAGAGGCTATA	10391
rs568748209	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68572697	GGTGAAACTGAGGCT[A/G]GTTTGGGGCCCACAC	10391
rs568751216	snp	A/G/T	0.000380878	0.0137953	intron-variant	CORO2B	GRCh38.p7	15:68719245	CCGAGGTACCACAGC[A/G/T]GGGGGCTCCACAGAG	10391
rs568765202	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68725482	TGTATTATTATAGAT[A/G]TAATAATACATCTAT	10391
rs568774065	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68638809	CTGCCTAGTTCTGCC[C/T]GCTGGACAGCAGCGG	10391
rs568776042	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68612896	CCCTTGCTCCTTGTG[A/G]CTCATTTTTCCTTAG	10391
rs568787706	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681382	GTCACAAGGAATGCA[G/T]GGAGGGGGCCAGTGA	10391
rs568813088	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612236	AAGGGTCTAAAAGTA[A/C]ATATGTGAATATGGA	10391
rs568838722	snp	A/G	1.66463e-05	0.00288494	synonymous-codon	CORO2B	GRCh38.p7	15:68718729	CGGGCTGGATGTGTC[A/G]GCCTGCGAGGTGTTC	10391
rs568899508	snp	G/T	0.00597247	0.0543191	intron-variant	CORO2B	GRCh38.p7	15:68724917	AGAGAGTCATTGGGG[G/T]GAAGATCTGCCAGGA	10391
rs568946269	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646554	GCTGCAGGGACACTG[A/G]GGACAGAGCCTGATG	10391
rs568956587	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68584681	TCCAGGAGATGAGAA[C/T]GTGTGCAGATTCTCT	10391
rs568959810	snp	C/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68558827	CCAAAGCCCTGCCTT[C/G]ACTGGCTGGGTAACA	10391
rs569013039	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68598707	ACCTAGCTCTCCTCT[A/G]TGCCTTCCCATCTCT	10391
rs569035979	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646060	ATTACAGGCATGAGC[C/T]ACTGCACCTGGCCCA	10391
rs569042245	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700628	GCCATAACTCTCCCT[A/G]GCATCTGGCAGAATC	10391
rs569046873	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68694241	GCAGGAGGTGTCATC[C/T]AAGCTGTACAATAAT	10391
rs569079595	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68564034	AGCACTACCCTGATA[C/T]GAAATCCAAACAGAC	10391
rs569097032	snp	A/C	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68652918	GTGCCTTGTATTACT[A/C]TTACTGCCATTTGGA	10391
rs569098247	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68560838	GTACGAGGGAAAAGC[C/T]TGCACAACCCGAGGG	10391
rs569100972	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68605753	TTTGAGATGGAGTCT[C/T]GCTGTGTCGCCCAGG	10391
rs569121038	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68563240	CACCTATAATCCCAG[A/C]ACTTTGGGAGGCCCA	10391
rs569157619	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68668288	GGCTGGGGAGGGGGG[C/T]GCTACAGGGGATCCA	10391
rs569217520	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654926	AGTGAGCTACCTCGA[G/T]GGGAAGGTACCCATA	10391
rs569219767	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68593051	TGGCAGAGGCATCAC[A/G]TCATAGTGAGTGTGT	10391
rs569225805	snp	A/C	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68648695	GAAAGGAAGAAAGGC[A/C]AAAGATATGAATAAG	10391
rs569239252	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68695584	AAGGGAAAGAATATG[A/G]ACAAGGAGGGAGGGA	10391
rs569260162	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703198	GCTCTGTCACCAGGC[C/T]GTCATGCAGTGGCGC	10391
rs569264767	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641398	CACAGATGCCTCCTT[C/T]CTGTGTCTACACCCT	10391
rs569274757	snp	G/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68592296	CCTTAGCACACATAA[G/T]GGAATTTTCTGAGTC	10391
rs569301749	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701741	TGCCCGCCTCGGCCT[C/T]CCGAAGTGCTGGGAT	10391
rs569309374	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595009	TTCTAGCTGTCCGTG[C/T]AGTTCTAGCTATCAG	10391
rs569318984	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68663844	TAGCATTCTTATTAA[G/T]ACAGAAGTTGAAATC	10391
rs569325949	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68708641	TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC	10391
rs569339788	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68608093	GTGAAATGCCACCAA[C/T]GTGAAAGAACATATC	10391
rs569374608	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68645913	CGAGAAGCTGGGATT[A/G]CAGGCACGTGCCACC	10391
rs569386659	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615632	TGATAAATCATGAAG[A/T]TTAAGGCCTCATGAA	10391
rs569396754	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68689864	ATACTCTACAGCCTG[C/T]AGCACTGCAAAGTGA	10391
rs569438308	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708265	GGAGGCACCAAGAAG[A/G]AAAATTTGTCCAAGG	10391
rs569444688	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68581189	GCTTCTTGGTATCCA[A/G]TAACTATTCAACACT	10391
rs569446290	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68579433	GATCCGCTCGAGTCA[C/T]TCCGGCCCCCAAGGA	10391
rs569457600	snp	A/G	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68642915	CCTCCTTTCTCGTCT[A/G]TGGAAACTGTGGCAT	10391
rs569459634	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614084	GTGCTTGTTAAAATG[C/T]GGATTCTTGGGTTCT	10391
rs569462313	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68627243	TATGATTTTGTGCTG[A/G]TCTCGTATGAGGGAT	10391
rs569462930	snp	C/G	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68700092	CCCTTCCCACGGCCT[C/G]CCTGCCTCCTTCAAA	10391
rs569487825	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707086	CTGCCTCAGCCTCCT[A/G]AGTAGCTGGGATTAC	10391
rs569543659	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68620514	TGTCCATGAGTCTGA[C/T]AAGTTATTTTAAGCC	10391
rs569558655	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566059	TGCACACTGAAGTCA[A/G]GCAGTCCCCTTCCCC	10391
rs569559305	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68558590	GTTGTTGCTCGGGCT[-/G]GTTTCAAATTCCTGG	10391
rs569598073	snp	C/G/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68713050	TTTTCTGACTTGCTG[C/G/T]CAACTTACCTGATGC	10391
rs569599983	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68586681	GATGAGGCTGGTCCA[C/G]ACCCGGACCTCCGGA	10391
rs569615342	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68689857	TCTAATAATACTCTA[C/T]AGCCTGTAGCACTGC	10391
rs569617022	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68682138	TCCCACCAGGACAGC[A/C]CACAGAGGGAGAGTC	10391
rs569644410	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68573674	ATGGGAGACCCACAT[A/G]CAGAGAAGGAGAGAC	10391
rs569649967	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656379	GTTGCTAAGCAACCT[G/T]TGCCTGAGTTTCCAA	10391
rs569663357	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622351	TACATTCCCTTGAGC[A/G]TGAGCTGACTGGGGA	10391
rs569665449	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68669507	GTATGCTTTGCGTGA[A/G]TGCATGAGTGGGCCA	10391
rs569683290	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68700433	CTGATTTCCCCAGCT[C/T]CTTCCCCATATCCCC	10391
rs569684295	snp	A/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68670068	TCTCAGAAAAAAAAA[A/G]GGGGGGGAAAAATAA	10391
rs569696009	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678417	GGTGGTTCACACCTG[C/T]AATCCCAACACTTTG	10391
rs569704338	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622995	CCCATTAATATCACC[C/T]CTCTTTTAAAGATGA	10391
rs569713645	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631047	GTGAGGGGTGTTCCC[A/G]TGGTGGTGCAGGGCG	10391
rs569721950	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68683343	TTGGTCCAGACCCCG[C/T]GTCCCCAGCACTCCC	10391
rs569722904	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662558	CAAGAGATCACTTTG[C/T]ATTGCCATATGCAAT	10391
rs569745103	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68677113	CGGGACTGTGCTCCC[C/T]GCCAGGCCTGGAGCC	10391
rs569748607	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630355	ACTGCATGGCAGGCA[C/T]GGGCAGCCGCATCAG	10391
rs569761484	snp	C/T	3.29761e-05	0.00406041	synonymous-codon	CORO2B	GRCh38.p7	15:68715250	CTACGAGATCAGCAC[C/T]GAGAAGCCCTACCTG	10391
rs569778254	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68623979	CCTCAGCTCAACCTC[C/G]AACAAGAAGGAGGAT	10391
rs569779137	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68676516	CAGACACCTCCATAC[A/G]CTGTCCCTGTTCCCC	10391
rs569870606	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68696481	TTGAACCTGGAAGGC[A/G]GAGGTTGCAGTGAGC	10391
rs569891799	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68727972	ATCTCAGCACTATTG[A/G]CATTTGGGGCGAATA	10391
rs569894570	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594352	TCCCATTTCTAGGAA[C/G]AGCAAGCTGTGGGTG	10391
rs569900960	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720066	CCAGCGGTATTTCGT[C/T]CCAGCCCACACCCCC	10391
rs569901344	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68635518	ACCAGATTCTACCAC[C/G]CCCAGGGCAGGAAGC	10391
rs569918737	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575097	CATAAGAACCAGGGA[C/T]TTTTTACTTTCTGCC	10391
rs569923657	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675833	CTCTGTACCCGGCAC[C/T]GTGGGAAGCACTGGG	10391
rs569933775	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726517	GGACAGCGAGCGGCC[C/G]GGCTCCTTTCTGTCT	10391
rs569945395	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623762	CGCATGCTGGATCAC[A/G]GCTGCTGGGTAATCC	10391
rs569969628	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589975	TGGCCCGTGACCCCC[A/G]GCTCTCCCTCCTGGA	10391
rs569972430	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68599276	ACTGCTCTGATGAGA[G/T]AGTTATATCTGAACA	10391
rs569975258	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68601712	GGCCGGAGAAGAAAT[A/G]AGGGCTTTGAGGAGC	10391
rs570016161	in-del	-/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68680251	ATATAGACTGGCATT[-/G]TGTTTGAGACCAGAG	10391
rs570053302	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703655	TGTAGCTGTGTAATA[A/T]GCAGCAGGTCCCTTA	10391
rs570101268	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614645	TCAAGGATGTGTCTG[A/G]AGGCTGTGCTGGAAA	10391
rs570101418	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68622301	CCAGCTGGGTGGACT[A/G]TGTGACTGCAGTGTG	10391
rs570138024	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68714394	CCCCTGGCTGCTTTT[C/T]GTGACAAGAAAGTCA	10391
rs570140411	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621750	GACAGTCACGTGACA[C/T]TGGGCAAGTTTCACT	10391
rs570152709	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68685025	GATGATAGGGGTGGC[C/G]CATGAAAAAACATCT	10391
rs570157864	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589536	AACGCCCATTTTGCA[A/G]AGGAGAAAACTAAAG	10391
rs570162036	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678020	CCCCTGGCCCAGGAG[G/T]CTGCCTTGCCCCTCC	10391
rs570173482	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595827	CGGATGAAGCCATTG[G/T]CTCAGCATTGAATGC	10391
rs570191586	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68572497	AACAACTCCTTCATA[A/T]CTGTTTTGCATGATT	10391
rs570221948	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68643223	CCACTTTGGGAATAG[C/T]TGGTGTCCTGATGAG	10391
rs570249380	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713783	CTTAACCACATCTGC[A/G]AGGACCCTTTTCCAA	10391
rs570292228	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697307	TTGATGATGGATAGA[C/T]GAATGAATGAAAGAA	10391
rs570310083	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68708209	CTGGCTCTGTGGGGG[A/G]AACACACATGAGGGA	10391
rs570320659	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68723014	AGAGGTTGCAGTGAG[C/T]GGATATTGCACCATT	10391
rs570325493	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594241	CCATAGGTGGTGCCT[C/G]TCTGTGCAGGAACCT	10391
rs570361679	in-del	-/TC	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68607310	CATCTACACATGGTG[-/TC]TCTCCACATGGCTTG	10391
rs570363478	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68593396	CCCCAGAACAATAGA[A/C]TCAGAATCTCTGAGA	10391
rs570436209	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68565030	ATTTTCCTAATTTAC[A/G]TATTTGTTGCTTCAT	10391
rs570453747	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600095	GTGCTTCAGGGATAA[A/G]AGATACTTGCAGATG	10391
rs570454319	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68628575	GACTTTACAATAGCT[A/G]CATGTATTAAGCCCA	10391
rs570464155	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637087	TACTCCCAAATGTTG[A/G]TTCCACAGATACATG	10391
rs570466755	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661809	GTCAGGAGTTCAAGA[C/T]CAGCCTAGCCAGCAT	10391
rs570471123	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702946	ATTCTCATGCCTCAG[C/T]CTCCCAAGTAGCTGG	10391
rs570479660	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68587437	CCATGATCAGTATTT[A/G]ACTCCGGAGATGTCT	10391
rs570493847	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68583588	TGGAAGAAGCATTGC[A/G]GGAGTGGGAGGAGGG	10391
rs570560801	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726037	TCATCCCTTAACTTC[C/T]CCCTTACCAGTGACC	10391
rs570579264	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675790	AAGAGAGAATTTATT[C/T]ACTTAACAAATTTTT	10391
rs570584809	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642529	TCCCCACTAGGCTGG[A/G]CTCCCTTCATGGATA	10391
rs570644931	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633572	GGGACAGCACAGGGT[A/G]GACAGTGCAAAGAAT	10391
rs570648467	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689086	GTACACAACAGCTGC[A/G]ATTCAACATTTGACA	10391
rs570670106	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641321	AGCTGGGCTGTGGGG[G/T]CAACAGGAGATGGAT	10391
rs570682044	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68604219	TTCCCTTGACGCATA[C/T]TCCAGGGCTCCAGCA	10391
rs570718070	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681504	GAAGTCTGGGAAAAG[A/G]TGGTCATCCAAATAT	10391
rs570732746	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640975	TGTGAAGACTTAGCA[C/T]AGGTTCACGTGGAGT	10391
rs570823611	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68658536	GTGCTTAACTCTTTG[C/T]ACCCACTCCCCACTT	10391
rs570827200	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727443	GTTTGGGGTGAGATC[C/T]GGAAATCAAGAAATG	10391
rs570853105	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684315	GGACTAACCCAATGT[C/G]CCCCAGTCCTCTTTG	10391
rs570873295	snp	A/C/T	0.00438476	0.0466401	intron-variant	CORO2B	GRCh38.p7	15:68588988	TACCTGAGTGGCCAA[A/C/T]TGATAACTTTATCAT	10391
rs570882233	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68692290	ACCCGCCTCTGCTTA[C/G]AGTCTCATTTTTTAA	10391
rs570882298	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68706921	TCTCACTGTGTTGCC[C/G]AGGTTGGTCTTGAAC	10391
rs570890121	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68670590	TCTGATATACAAAGA[A/G]CTCTTATAAATTATT	10391
rs570905113	snp	G/T	0.0107246	0.0724382	intron-variant	CORO2B	GRCh38.p7	15:68719066	GTGACTGGAGATCAG[G/T]AAGAAGAGTCTGACT	10391
rs570907300	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703237	CTCACTGCAACCTCC[A/G]ACTCCCTGGTTCAAA	10391
rs570911899	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595703	CATCAATTAAGCACC[C/T]GCTCCATGCCAGGCT	10391
rs570927145	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68672612	ACAGAAATGTCTGAG[G/T]ACAGTGAATTCATCT	10391
rs570943386	in-del	-/ATCT	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68676751	TAGAGGTGGCCCAAG[-/ATCT]GTGTTTTTTGTTTCT	10391
rs570961307	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690935	GCCAAGTGGGATTAC[A/G]GGTGTGAGCCACTGT	10391
rs570994592	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561129	CTCTCAATACTGGTT[A/G]GGTCCCAGGAAAGGG	10391
rs570996209	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595097	GTGGATTTAGGAAGC[A/G]TTGTACCATGCAAAG	10391
rs570997127	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559753	GCCCGAGACCGCTCC[A/G]CGTGCAGCTCCACGG	10391
rs570999762	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609655	GCCAGGCCTGAGCCC[A/G]CTGTCCCCTCCCCAC	10391
rs571012341	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68650280	AGCTGAGGCAGGAGA[A/G]TTGGAGGCGGAGGTT	10391
rs571017457	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68655893	CAGCACTTCAAGGAA[C/G]AAAAATGATTTAGGG	10391
rs571024320	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690044	ACTAAATATTAAAAA[C/T]GTATTACTTCCCAAT	10391
rs571033780	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68624681	GCATCTCTGTTTTTT[C/T]TTTTCTTTTCTTTTC	10391
rs571039031	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68686492	CACCTTGGGCAAGTC[A/G]CCTCCCAGAGCTCAG	10391
rs571081064	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662440	TTTTATTTTTTTACA[A/G]TAGTCCTTAAGCTGG	10391
rs571108054	snp	A/C	0.0879971	0.190408	intron-variant	CORO2B	GRCh38.p7	15:68703057	GTCTCGAACTCCTGG[A/C]CTCAAGTGATCCACC	10391
rs571116719	snp	C/T	0.00676609	0.0577691	intron-variant	CORO2B	GRCh38.p7	15:68671399	GAGCCAAAGCCTCAC[C/T]CACATGGCTTACCTG	10391
rs571134568	in-del	-/GA			intron-variant	CORO2B	GRCh38.p7	15:68607639	CCTGGGTGACATAGC[-/GA]GAACCCATCTCTACA	10391
rs571136163	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68565853	CTGATGGTTCCCCAG[C/T]TTCCCCCTCTCCCCT	10391
rs571147886	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664429	AAGACAGGCGGATCA[C/T]GAGGTCAGGAGATCG	10391
rs571201627	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604314	TTGGTTCCATTCTTC[A/G]TGGTCAGCCCCCACC	10391
rs571217433	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651193	AGGGTCCCGCCTCCA[A/G]AGCGGGATGACTTAG	10391
rs571222853	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603683	AGAGCTCACTCTCTC[C/T]GCATCTGCACAGAGG	10391
rs571223930	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651720	TCCTCTCATTCCTTG[A/C]TTGCTTTTCTAAGAG	10391
rs571251930	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644341	ATTGGATTCAGTAGG[G/T]CTAGATTGGGACCCA	10391
rs571287128	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68657953	AGGCAGAACTGCTGT[A/G]GCTGAAAGTTGGTGG	10391
rs571298390	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68619195	AAGCCCAGAGCCCCA[A/G]TCTGTGTTACTCTTC	10391
rs571306983	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68698872	CAGAGGGGCAGGGCC[C/T]ACCCCACCCACCAAA	10391
rs571316541	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703860	AACAAACTTCATATC[A/G]TATGTATTGACTACA	10391
rs571333571	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68610936	TTCCACACCCTCGAC[A/G]CAGCCAAGGAAAGAA	10391
rs571365028	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68617413	CTGGGAACCAAAGGA[C/T]TTGGTTCTAGTCCCA	10391
rs571370327	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704355	TTATTCTTTGGTCAT[C/T]TGCTTGGTAGTGTAT	10391
rs571397880	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585253	GATGACCACACCCTG[C/G]TCCCAGAGCTAATGT	10391
rs571427405	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68708916	GAGCTCCTGGGCTCA[C/T]GTGATCCTCCTGCCT	10391
rs571431442	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68575045	CAGCTTAGAGCATCT[A/G]AAAGAGCCCAGACTT	10391
rs571445380	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623658	TCCAGAAATCCTGTT[C/G]GGCGTCTCCATCCCA	10391
rs571491470	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68709559	GCGCCTGGCCTCAAG[C/T]GATCCTCCCATCTCA	10391
rs571503967	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717567	AGAATGACTCACTTC[A/T]TCCTCATCCTCATCC	10391
rs571517171	snp	C/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68582857	GTGTGCTGTGTTAAG[C/T]TAGACGCTAGTGAGC	10391
rs571522243	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591074	GGGATCCTGGTCTGT[G/T]GGGGGACACAGGCTG	10391
rs571525740	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68570268	CTTCATGGGATCCTC[A/G]GAAGGAGCAAGGGAG	10391
rs571560624	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577143	CTACCCAAGAGATTT[A/G]GTAAGTCCCTGGAAC	10391
rs571565924	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68643766	CAGGCCAGGCGGCAC[C/T]GTGGCTCACACCTGT	10391
rs571575354	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705259	CCTGGCCAACATGGC[A/G]AAACCTTATCTCTAC	10391
rs571577479	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68625846	CTGAGCTCAAGCAAT[C/G]TGCCCCCCTTGGCCT	10391
rs571577819	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705585	CCCTCAAGCCCTGCC[C/T]GAGACCCTACATCCA	10391
rs571580374	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623122	GTGAGCCGAGATCAC[A/G]CTACTGCACTCCAGC	10391
rs571593173	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589515	ACTTTAAAGATGTAC[A/G]GTAGAAACGCCCATT	10391
rs571599149	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68685949	CCAAGAACAAATCTA[A/G]GGGGCTTCGCAACTG	10391
rs571601788	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68716178	TTTACTCTTCCCCAA[C/T]TCTGTCATCCCCACC	10391
rs571610160	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68685306	ACCTCCTCCTCCTGG[A/G]TTCAAGCCATTCTCA	10391
rs571616380	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68692887	GATCCACCCGTCTCA[A/G]CCTCTCAAAGTACTG	10391
rs571625847	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68694743	CTGAGCGTGCGTGAA[C/T]AAGGCAGATCGTGGG	10391
rs571645390	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68659446	GACTGGACACAGTGG[C/T]TCATGCCTGTAATCC	10391
rs571683703	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595290	CCAGCTAAGCCCTGC[C/T]GTCCTGTGTCCCTGA	10391
rs571693790	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68602891	AATCTTGCAAGCACA[C/T]GTGTTTCCCTGGTTG	10391
rs571707104	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68658671	CCCTGAGCTTCATTC[G/T]TCTTTGTCCAGTAGA	10391
rs571709289	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68568661	CATTAGCTCATTTAC[C/T]GCAGCCTGAGACTTG	10391
rs571711446	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667268	CTTCATGCTCCTCTC[C/T]GCACAGCTCAGGGCA	10391
rs571727047	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68697409	AAATTAATATAGTCC[A/G]TCTAATCAGTTATCC	10391
rs571742366	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68649550	GCGTTCAGTCTCAGG[A/G]TCACTTTCCACTCTT	10391
rs571753870	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727043	GAGGCCTCGTCCTCC[C/T]GGAAGCTGAGGCTGA	10391
rs571759700	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597749	GCAGAGAGGAACCTC[A/G]GGCAAAAGTCCAGCC	10391
rs571762958	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68620033	TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA	10391
rs571769134	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68583752	CCTCCAGACATTCTA[C/T]ATCCCAGCACCTCGT	10391
rs571771571	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68565874	CCTCTCCCCTGGGGC[C/G]TGGCTGCTTCCTCTG	10391
rs571772242	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68602209	TCCTGAAGTGGGAGT[G/T]GGGGGAACTGCTGAC	10391
rs571772655	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68608310	GCCCAGACCCGAACA[C/T]TGGTGGTTACAGTTT	10391
rs571780063	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68604641	AAAAACCTCCCTTCT[A/G]TGTAAATTCAGCCCC	10391
rs571799788	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597806	CAGTGGCCTGCACAG[C/T]TAGACCCATTGCTCT	10391
rs571819727	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723327	GGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTTG	10391
rs571839762	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68679256	TGTGTTTGGTGAGCT[A/G]GGTGGAGATTCAACA	10391
rs571863060	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68650845	TCAGAGGCCCTACAG[G/T]CCAGAGAGGGGCTCA	10391
rs571864036	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68646609	ACTTGATGGCGGGAG[A/G]TCTGGGTTCTGCCCT	10391
rs571867020	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702494	GCAAACAGTGAGTCC[A/G]GTGCTCAGAAGATGT	10391
rs571882179	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68638832	AGCAGCGGGGCTGAC[A/G]GAGGTGGTGTCTGGA	10391
rs571912474	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68573783	CTTCATTCTCCAGGA[A/G]CTTGTCAAATACACA	10391
rs571913889	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68683087	ATGGCAGAAACCCAG[A/G]CCTCTGGGCCAAAAA	10391
rs571944744	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68644971	TGAAACCCACTAGAA[C/T]GGGCTGGGCATATGA	10391
rs571949924	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68597218	TCGCCTGGCTGCTGG[A/C]ACATCTTTTCCAGGC	10391
rs571964204	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691048	AGAAAACTGGTTTTC[A/G]GCCAGGTGCGGTGGC	10391
rs571994143	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637999	ATAGTGATTATCTCA[A/G]AGGGGAGAAAAAGCC	10391
rs572027926	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68690457	CCCTATTATGGAAAA[C/T]GAGGCTCTAGCTTTT	10391
rs572035512	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580643	AGGGCTGTTGTGGCC[C/T]ACCTGGGGTAAGATG	10391
rs572083302	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559845	AGGTCTCCCGCAAAC[A/G]CGCGCGCACGGAGAG	10391
rs572160598	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68624557	AACTAATATATGATG[A/T]ATTAGTTGTGCATTC	10391
rs572196743	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615806	TCCCAACCTCCAGAG[A/C]CATGAGAAATAAATT	10391
rs572226251	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68623822	TGGAGGCGGGTGTGT[C/T]TGAGCAGCCCCAGCC	10391
rs572247480	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68624495	CTGTTCACAGTGTTT[C/G]CTCCAGCCTGGAACT	10391
rs572258507	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669217	GCAAGCAAGCCGGAG[A/G]CAGGACTCGGCCTTG	10391
rs572259503	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630385	GCACACCCCAAGGAA[C/T]GGTGCTGAGGGATGA	10391
rs572261484	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68623332	CAATAGAGCAGGGGC[C/T]TTGACTGAAGCTGCT	10391
rs572298144	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669588	TTTGGCCTCACTTTC[A/G]TTGAGCTCAATGGGC	10391
rs572299156	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622542	TCTTTAATTGCCTTC[A/G]GCAATGGGGAACTCA	10391
rs572328119	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68629597	GTGCTGGGGATGAAA[C/T]GATGTGCAGGGAAAG	10391
rs572345113	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648637	CCTGGGCCACAGAGC[A/G]AGACTCCGTCTCAAA	10391
rs572417885	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631606	AGCTCTCAGAGCTGA[C/T]ACCAGGGCCCAGCTT	10391
rs572430144	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68698532	CTGCATCCCCGGCCA[C/T]ATGAGCCAAGAGACT	10391
rs572454434	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68595947	AAGGAGCAGCGTGAG[C/T]AGAGGCCAGGGCAGC	10391
rs572499932	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664571	AGAATGGCGTGAACC[C/T]GGGAGGCAGATCTTG	10391
rs572516216	in-del	-/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68627799	TGCCATAGACCCTCA[-/G]GCTTATGGGTACAGC	10391
rs572529681	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576210	GCATGTATTTCTCAG[C/T]ATCTCCTACATGCAG	10391
rs572535492	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68673076	CAGGGGTGGTGAATG[A/G]GGGCCACTGTGAGTG	10391
rs572542231	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68708943	GCCTTGGCTTCCCAA[A/T]ATGCTAGGATTGCAG	10391
rs572598953	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574691	CAAGTGTCAGCCTTG[C/T]GATTTTAAAAAAGAG	10391
rs572646860	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678095	CCTGACAAAGGCCTA[A/G]CATGCACTTGACTTT	10391
rs572662108	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589075	ATCTGGGAACAAACT[C/G]AAGTTATTATGGATT	10391
rs572678030	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636666	TGTTTGTCAGAGATG[C/T]AGAGAAAGACAGTGG	10391
rs572748706	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68644467	AAACCTTGCTCCAAA[G/T]GGTAATCTGGCATAG	10391
rs572760365	snp	G/T	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68677539	AGATGGTGGCGGGGG[G/T]ATGCTGAGGCTGTGC	10391
rs572763165	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68651932	GCCGTGTCTACAACA[A/G]CTACAAACAACAACC	10391
rs572763255	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68686823	AGAATCGCTTGAACC[C/G]AGGCGGCGGAGGTCA	10391
rs572768329	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68593209	TTAATACTGTTACAT[C/T]GGCAATTAAATTTCA	10391
rs572773967	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68584934	GTGGGCCTGGAGTGC[A/G]GGACCAGCTGCTAAG	10391
rs572796308	snp	C/T	0.000972132	0.0220255	intron-variant	CORO2B	GRCh38.p7	15:68711525	TGACCCTGCCTCCCA[C/T]GCATCTGCCCTCGCA	10391
rs572823434	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68639214	TCTTGCCCCCCTACC[A/G]TACTGAGAGATGATT	10391
rs572857397	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68584003	GGCTAGCAGTCATTC[A/G]TTCATTTAGCCAGCA	10391
rs572857945	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68686121	TGGCTCATTGCAACC[A/T]TCACCTCCCGAGTCA	10391
rs572883190	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717875	GGTCTGTGCTCGTCA[C/T]GGTGCCAGGCAGTTA	10391
rs572889013	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68662931	ATACCTTTTTCTTAA[-/T]TTTTTTTTTCCTAAA	10391
rs572913837	snp	A/C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68624624	GAGTTCCTGGGGTCC[A/C/G]TGCCCAGAGATTATA	10391
rs572921170	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703555	ATATCAGATCTTCTC[C/T]TAGCTGCTTAGGCCC	10391
rs572932954	snp	A/G	0.0115144	0.0749975	intron-variant	CORO2B	GRCh38.p7	15:68590471	GGCCTGCCCTGCTTC[A/G]CACAGCAGGAAGGGG	10391
rs572944108	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717444	ATAGGTGGGGAGAAG[A/G]AAGACGGGGAGAACA	10391
rs572945797	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723537	TCGGCTCACTGCAAC[C/T]TCCACCTCCCGGGTT	10391
rs572961618	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68685544	CTCACCCTCCCCAAC[A/G]TGAGACAAGACCAAC	10391
rs572965378	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68598872	CGGGAAGCTGGTGGG[G/T]ATGGGAGCTGGGGCA	10391
rs572985073	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68694456	AAAATCAGCAGAGCT[A/G]TAATTCAAACACAGG	10391
rs573047930	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693922	CTCACCGCAACCTCC[A/G]CCTCCTGGGTTCAAG	10391
rs573055460	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68611139	TTCTCTATATGTACA[C/T]GCATGTTGGAGATGA	10391
rs573055898	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68723016	AGGTTGCAGTGAGCG[A/G]ATATTGCACCATTGC	10391
rs573060250	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68700488	CAATCCCCGTCCCCC[A/G]GGATCCGTTTCCCCT	10391
rs573066533	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68562948	TGCCACTGCACTCCA[A/G]CCTGGGCGACAGAGC	10391
rs573067902	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577065	TGGCAGGCAAGCAAC[G/T]TGGGAAGATGCCTTA	10391
rs573079613	snp	A/G	0.00358779	0.0422022	intron-variant	CORO2B	GRCh38.p7	15:68658165	GTCCTCCAAGGTCTC[A/G]CCAGCTCTGACATTC	10391
rs573096021	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566405	AAGCCTTATCTTCCC[A/G]ATCACCACCCAAAAT	10391
rs573100340	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68691855	AAGCTCCTGTTATCT[G/T]ATGGCCACCTATTGA	10391
rs573122524	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68687862	AAGACAACTAACCCA[C/T]TCCCAAGATAAAGAC	10391
rs573140517	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68604426	TAACAAGGGCAAAGA[C/T]TGCCATCACTGAGGA	10391
rs573154426	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68632893	CACCACACCCGGCCA[A/G]TAAATGGATGTGAGT	10391
rs573175371	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603855	TTCTGTTATGGCAGC[C/T]TGAGCAGGCTAATAC	10391
rs573209242	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68613468	CCCTTCTTTCTCTCT[A/T]TGTGGCAAAGCTTGA	10391
rs573242167	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68585399	CAGTTATTAAGCAGG[C/T]GTTGGGCACGCATGA	10391
rs573274479	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678729	TCCAGGGATCAGCAG[A/G]TGGCATAGCCAGCAC	10391
rs573288575	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68647675	GCCTGGGCAACAAGA[A/T]CGAAACTCCATCTCA	10391
rs573317421	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583332	ATGAGGGAACTGAGA[C/T]GCTGGGAGCAGAAGT	10391
rs573324491	snp	A/G	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640149	TTCTGCAGACACCCA[A/G]CTTTGGCCCACAGTG	10391
rs573342765	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68607725	TGGGACGCTGAGGTG[A/C]GAGGATTGCTTGAGC	10391
rs573386439	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68685491	TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC	10391
rs573388242	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68603553	ATGTTGAAGCCCTAA[A/C]CCCCAGTGTGTTTGG	10391
rs573392172	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68659627	TTCATTAAGTGGAAG[C/T]GAATCATTATAAAAG	10391
rs573409946	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612034	CCTCCACTGCCCAAA[A/G]TGCAGAGGCTATAGG	10391
rs573449699	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68684709	CAAGTGGTGTGACCA[G/T]GGGCAAGTGTCCTTA	10391
rs573451677	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68643891	AAAATGCAAAAATTA[G/T]CTGGGCGTGGTGGTG	10391
rs573489754	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68712073	ACTGCCCAGCCACTT[C/G]ATAGGATGAGCCTGA	10391
rs573511347	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68671218	ACTCACCACGACATA[A/G]TAGGAATTATTCTTC	10391
rs573516446	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68705331	TAATCCCAGTTACTC[A/G]GGAGGCTGAGGCAAG	10391
rs573541273	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68561260	CTCCTGCATATGCCA[C/T]GCTGGGCGGCCCCCC	10391
rs573557261	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68657426	GGAGGCTGAGGTTGG[A/T]GCATCACTTGAACCC	10391
rs573557833	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68717360	AGAGAGAATGGATTT[G/T]GGAGGGGCAGGAGGA	10391
rs573566351	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68618345	TTACACATGTTGTAT[C/T]ACATGTAAATCATGT	10391
rs573577553	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68560691	ATACAACCCATCTTC[C/T]TCCTCTCTGCTCCTT	10391
rs573577908	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68590377	CCATGCCCAGCCCTG[C/T]ACTTCTGTTCTCTCA	10391
rs573592455	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68618779	AGGATTTGAATTCAG[G/T]CAGTTACATTGTGAT	10391
rs573608038	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68722430	CTGTCAAAGGTGGAC[A/G]CATTGATCTAAGTGT	10391
rs573614118	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68597337	TAATGCTTATTCAGC[A/G]CTTACCATGTTCCAG	10391
rs573617439	in-del	-/TGTC			intron-variant	CORO2B	GRCh38.p7	15:68665560	ATAAATTAAAGAGAA[-/TGTC]AACCTTATGATGTTG	10391
rs573620032	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664508	AAAAATTAGCCGGCC[A/G]TGGTGGCAGGCACCT	10391
rs573622455	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68644416	CCCCAACCCCAGATG[A/G]CTTTGATACAGGTGA	10391
rs573683901	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68605763	AGTCTCGCTGTGTCG[C/T]CCAGGCGGGAGTGCA	10391
rs573714229	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68700267	ATACAGGGCTGGGGA[C/T]GGCGCCAGGCCACAG	10391
rs573733322	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68691823	CTCCAGTGTATCGCC[A/C]GTGGGCTGCTGGCTA	10391
rs573760061	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68643760	CAAATGCAGGCCAGG[C/T]GGCACCGTGGCTCAC	10391
rs573774939	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68691198	GCCGGGCAAGGTGGC[A/G]GGCGCCTGTGGTCTC	10391
rs573794202	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68728229	GCTCTACATTGGAAC[A/G]GTGCCTTGAAGTTTA	10391
rs573803949	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68611971	AGACTGGGTCTTGCT[A/C]TGTTGCCCAGACTGG	10391
rs573824513	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68699930	CATTTACATCACAGC[A/G]TCTGCTCTCCTCAGG	10391
rs573868968	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68707324	CTGTGGGTTAAAAAC[C/T]AGGACAGTTTTTGGG	10391
rs573878502	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68709389	AAATGGTATCTCAAA[A/G]CTGTTTTTCCTGTTT	10391
rs573905688	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68689305	GTTCTCTAACCAGAT[G/T]GCAGGTTAGAGCCCT	10391
rs573934159	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68646128	GAAATAATTTACCTT[C/T]TTCCCCATCCCCCAC	10391
rs573958116	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68610511	TCTTTCGCTCACATC[C/G]CCTCCCTCATACATC	10391
rs573960701	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595839	TTGGCTCAGCATTGA[A/G]TGCGAGTCCTAAAGG	10391
rs573985286	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68576077	AGAATCGCTTGAACC[C/T]GAGAGGCAGAAGTTG	10391
rs573995198	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693343	TCATCTCACTGGGAA[A/G]TGCCAGGCATGTGCA	10391
rs574022683	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68611084	ACATGAGAAAATGCG[A/C]CCCACCACTGAGCCA	10391
rs574023568	snp	G/T	1.64887e-05	0.00287125	missense	CORO2B	GRCh38.p7	15:68645283	GACAACCACTTCTGT[G/T]CCGTCAACACCCGCT	10391
rs574042365	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68686258	CCAGGCTGGTCTCGA[A/C]CTCCTGACCTCAGGT	10391
rs574093683	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652021	GATCCTCTCAGCAGG[C/T]GGGTACAGCCATCCC	10391
rs574120375	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569848	TGCAGATGAGGAAAC[C/T]GAGGTGCAGAGAGTG	10391
rs574156840	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68711466	TTCTCCCAGGGCAGT[A/C]AAGTGTGCACTGGGG	10391
rs574182244	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569154	TCATTATCACCCAGA[A/G]TCCAGAGTTTACATT	10391
rs574189282	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68599160	TTCTGCTCCCTCTCT[A/G]CTTGAAAAGTCTGAT	10391
rs574203393	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68658761	TAAAGTACCCCAGCT[C/T]AGTGCTGACTCAGTG	10391
rs574224349	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68713104	GAAATCAAGTGTCAC[A/G]AGCCAGTGGGCAGGA	10391
rs574250123	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68673025	CAGGAGAACCCACAC[C/T]CCCAGGGAAAGGGTC	10391
rs574280726	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68564580	GCCTCCTACAGTGCC[A/G]GGATTACAGGCATGA	10391
rs574296524	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68624570	TGTATTAGTTGTGCA[G/T]TCAAATCACCTTGGG	10391
rs574303507	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725080	AAAGTTCTAAATTAT[C/T]AGCACAAGCCGGGCA	10391
rs574317551	in-del	-/CACACA			intron-variant	CORO2B	GRCh38.p7	15:68704075	ACACACACACACACA[-/CACACA]AATACAAATATTAGC	10391
rs574348389	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613461	AGAACTTCCCTTCTT[C/T]CTCTCTATGTGGCAA	10391
rs574407002	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68569985	CATTGGTCAGTGGGG[C/T]CTGTGGCCTTGGGAA	10391
rs574461883	snp	A/G	0.000810208	0.0201109	intron-variant	CORO2B	GRCh38.p7	15:68675944	GGATTATAGGGTATA[A/G]TATAGTATAATAATA	10391
rs574464990	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570716	TTTCCCTTAGGGAAG[A/G]AAAGGGTCTGTGTTC	10391
rs574477080	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68700942	TTTATTCAAGCTCTT[C/T]CATCCTGTGTCTGCT	10391
rs574481705	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667694	CCCTTCTCAGCCTCA[A/G]TTTCCCCATCTGTGA	10391
rs574489343	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68571235	TTCTGTACTCAGTAC[C/T]CAATATTCAGTACTC	10391
rs574491831	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68619835	TAGGTCTTTCCTTGC[A/T]GTGTTCTCTCCTTTT	10391
rs574506892	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68579831	ACAGGGCAGGTCCAG[A/G]TGGTTGGCTTGAAGA	10391
rs574535876	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68625523	TTTTTTTCCAGAATA[A/T]TATATCAATGGAATC	10391
rs574569960	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600164	CAACAAACAAACAAG[A/C]CTCCATCTAAAAACC	10391
rs574576386	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68675338	TCAATTCCCTTTCCT[C/T]GGTCAGTTCAGCCTC	10391
rs574596147	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68674608	CTGGACTTGCACTGG[C/T]GGTGGGGTGGAAGAG	10391
rs574606522	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591906	TCAGGAGCTCCTGCC[G/T]AAACCCTAGCCCTGA	10391
rs574614833	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640070	AGGAGTCTTTTCTGT[C/T]CCCTGCCTGCGCACC	10391
rs574637772	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631930	CAGATGGCCACCAGG[G/T]AGGGCCACATGCCAT	10391
rs574654955	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674100	AGAGGCTGCGTGTGT[A/G]TCTCGGGTCCTGGTC	10391
rs574724507	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68591569	TCTGTCCCTACCCAC[A/G]TTGCCCTAGAGGCAG	10391
rs574737636	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68647407	ACAAGAAAAAGAACC[C/T]GACCGGACACGGTGG	10391
rs574747827	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68654440	AGTAGCTGGTTCACT[A/G]GGACTCTGTGAAGTC	10391
rs574759076	snp	A/C			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577250	GGACCCTGCAGTTCA[A/C]GGATTCAAAGCACAA	10391
rs574768093	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68680512	CCCCTTGAGTTGTGC[A/G]GTGTACAGTCCATGC	10391
rs574772942	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68557692	TTCCATTCATTATCC[C/G]TTTGAAGCACAGAGA	10391
rs574785642	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68581041	TGCACTGCTCTGCAT[C/T]GTTGGGCATCCTGGC	10391
rs574801715	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587002	AATCTTTCTTATTAT[C/T]TATATTGGGCCTTGG	10391
rs574834548	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68624890	GTTTTGCCATGTTGG[A/C]CAGGCTGGTCTCGAA	10391
rs574836115	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594415	TGAGCTGTGCTCTCC[A/G]GCTCTCACCAGGTTC	10391
rs574846260	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641484	AGGAAGCAGAAGGAG[C/T]AGGGAAAAGGAGAAG	10391
rs574892441	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688612	TCTGTTTTACTAAGC[A/G]TAGATCTTTAGCAAT	10391
rs574896027	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68720180	AAATGGAGATGGCTG[C/T]ATGACCCCACCTGCA	10391
rs574906418	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68657911	GAAATAAAATCAGAG[A/G]GAAATATTATTGTAT	10391
rs574921253	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68667593	GATGGCAAAGCTTTG[C/G]ATTTAAAACCCTGCG	10391
rs574922055	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68689285	TGAGACTGAAGTTCT[C/T]TGAGGTTCTCTAACC	10391
rs574959074	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726178	CCAGCTTCTGGAGAC[A/C]CCCTGCCGGCAGCCC	10391
rs574979864	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68560945	TTCCCATGGCACAGC[C/T]CGGGTAATTTTCCCT	10391
rs574984983	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68659745	TCAAGACCAGCCTGG[C/T]CAACATGGCGAAACC	10391
rs574987955	snp	C/G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68704990	TTTCAACAAATCCCT[C/G/T]GAATACTAAGGGATT	10391
rs575019219	snp	A/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68558302	CCTGGCAGGCCCAGG[A/G]GTCCTGCTGGAACCC	10391
rs575052126	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68703786	AGATCTAACCAGACA[A/C]CTCCATAATCATGTA	10391
rs575070829	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600339	CAGCCCCATTCTGCC[A/G]CTGTGCTTGGTTTGT	10391
rs575072892	snp	A/G	0.000399281	0.0141238	missense	CORO2B	GRCh38.p7	15:68725870	TTCTTCCGGCAGCAG[A/G]ATGAGATTCGACGGT	10391
rs575095798	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68661159	ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC	10391
rs575098383	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68639442	GAGGTGGCTATTGCC[A/G]TGTAAGAGCTGTTGT	10391
rs575166228	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688268	TAGTAATATCCAACT[A/C]TTCAGATGTTGTCAC	10391
rs575166569	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68626105	GTAAATCTTTCTGCA[C/G]GGGCTGCTTCAAAAG	10391
rs575216416	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570002	TGTGGCCTTGGGAAA[C/G]TTCTCACCTGCAGAG	10391
rs575221300	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68606542	TTGGTCAGGCGCTTT[C/T]CTTAAAGTAAACATT	10391
rs575241833	snp	A/C	0.0185938	0.0946107	intron-variant	CORO2B	GRCh38.p7	15:68701468	AGGCGCCTGCAACCA[A/C]GCCCGGCTAATTTTT	10391
rs575249611	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68709606	GGACTATAAGCGTGC[A/G]CCACTACACCCGGCT	10391
rs575250044	in-del	-/TG	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578198	CACACAGGACGCACC[-/TG]TGTTATCACTCCACC	10391
rs575286808	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68665110	TCACTACTTTTAGAA[C/T]TTCATTCTTATATTT	10391
rs575294034	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68589199	TGTGATCCCTGGTAT[A/G]CCAGCCAGCAGGTAA	10391
rs575300373	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68673292	TATGATACCAGCATT[A/T]TGGAAGGCTGAGGTG	10391
rs575309941	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585279	AATGTGGGTCAGAGG[C/T]GGGATGCACGCCCAG	10391
rs575320257	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681209	GAGAGCAAGATCTCC[C/T]TCCATCTCAAAAAAA	10391
rs575348586	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625875	CTCCCAAAATGCTGG[A/G]ATTACAGGCATGAGC	10391
rs575349490	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68618916	AGGAAAACATTTTGC[A/G]ATTTTGAGAAAGGGA	10391
rs575359082	snp	C/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68679812	GGACTGGTCATCTCA[C/G]CATGGGGCTGTTCAC	10391
rs575365564	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585431	CGCATTTACTCTGTA[C/T]AACCATGGGGTAGAT	10391
rs575377169	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717955	TTGTCCTCCTCGAAC[C/T]AGCCAAGGAACTGGA	10391
rs575380931	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68557610	GGGAAGGGCAGCATC[C/T]TAACCAGAGCAGCAG	10391
rs575382431	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68688012	CCATAGCACCCTCCA[A/G]ACCATCCATTGGTAA	10391
rs575402987	snp	A/G	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68557526	AGTCTATCCAAGGTC[A/G]TACATCTGGAAAATG	10391
rs575452528	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68605144	AAAAGAAGTTTTGAA[A/G]AGAAAAACTTCAATC	10391
rs575455864	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68585048	CCCCTGGAGGGACTT[G/T]GTAATTGGTTTCTGG	10391
rs575540207	snp	C/T	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68597624	TTTCTGTTTCCCCCC[C/T]ATCAAAAAAAAAAAA	10391
rs575549385	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68562320	CCAGGCAAGATTGTA[C/G]TGCTCCTTCCCTTCC	10391
rs575552584	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627077	TGCCTCTGTTTCTAC[A/G]CCTGCAAAATGGGCA	10391
rs575577728	snp	C/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68590752	GGAAGGAAAACACTA[C/G]AGTAGGTGCAGGAGG	10391
rs575606563	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592856	ACCCCGGCTGCAAAT[C/T]ACCTGGTGAGGTTTA	10391
rs575615338	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68608896	AGCCTCCATCCATCC[A/G]TTCAACAAGTGCTTA	10391
rs575617193	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68624316	CCCAGGGAGTTTGAG[C/G]CTGCAGTAAGCTATG	10391
rs575635381	snp	A/G	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68628123	ATATTAGTAATAACA[A/G]TGATAAATATTCAAC	10391
rs575644703	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68725259	CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGC	10391
rs575659357	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68693261	TGGAAATGAGCCGAC[A/C]GAGATGCAGGCAGGA	10391
rs575694811	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68599689	GCCCCTCAGACCTTC[C/T]ACCCAAGAGAGGCAG	10391
rs575700649	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68694495	ACTCCGAAGACTATG[C/T]TTTCAACCACAGGGC	10391
rs575705435	in-del	-/T/TT	0.535466	0.205444	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630422	CCTCGAAATGAAATG[-/T/TT]TTTTTTTTTTGTTCC	10391
rs575712537	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641133	GTGGAGAGGCCAGCC[C/G]AGGCTTGCTGAGAGA	10391
rs575727369	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68646940	TGTTGCCTCAGGGAC[A/G]CACTCAGCTCCATCC	10391
rs575745004	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614765	TTCCAGGGCTGCAGC[A/G]GGCCCTTTATCCGCT	10391
rs575762173	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68700785	GCTCCCAGCCCTTCT[C/T]CTGGGGCCAGCAGCC	10391
rs575777621	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68598962	TAGGAGAGTGAGGCT[A/G]GGGGTTAGGGGATCC	10391
rs575833365	snp	A/C/G	0.000116633	0.00763573	intron-variant	CORO2B	GRCh38.p7	15:68714051	GACCAGGTCAGCCAC[A/C/G]GGGAGGCCTGCTGGG	10391
rs575833538	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707236	ACAGGTGGCATTTTT[C/G]ACCTATCAGATGGGT	10391
rs575850193	snp	G/T	0.0023933	0.0345097	intron-variant	CORO2B	GRCh38.p7	15:68580551	TTTGCCATTGGCCCT[G/T]GTTCTGGGACTTGGG	10391
rs575851298	snp	A/C	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68653351	CTCTCTTGGACCGAG[A/C]GCCCCCAACGGTGGG	10391
rs575879644	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68570652	AGTACAATGAAGGCT[G/T]TGGAAGCTGTGGTCT	10391
rs575882729	in-del	-/A	0.316243	0.241064	intron-variant	CORO2B	GRCh38.p7	15:68607818	GTGAGACCCTATCTC[-/A]AAAAAAAAAAAAAAA	10391
rs575885278	in-del	-/T	0.00716266	0.059414	intron-variant	CORO2B	GRCh38.p7	15:68620086	TGGCTAATTTTTATA[-/T]TTTTTAGTAGAGACG	10391
rs575890468	snp	A/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68571167	GAGTTTCTTTGTTAG[A/T]TTCTGAGGAATTTCC	10391
rs575921791	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68700544	AGTCTATCCTCCATC[C/T]CGCCAGGGATCCAGC	10391
rs575929679	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601510	GGCCATGAGCGTGCA[G/T]TGCGAGGAGGGCTAG	10391
rs575963643	snp	C/T	0.00398564	0.0444627	intron-variant	CORO2B	GRCh38.p7	15:68586838	GCCTCACGGAGCCTC[C/T]TTGGGCTGTGTAAAG	10391
rs575980867	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68613368	TGTGATGGTAGAAGC[A/G]GCATATTAAAATGGC	10391
rs575997333	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68648418	TTGGGAGGCAGAGGC[A/G]GGTGGATCACAAGGT	10391
rs576011020	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68564911	TGAAAACCACTATGA[A/C]TGATCCTGAAGAAAC	10391
rs576019404	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68612623	AAGTCTAGAAAGAGC[A/G]CTGAACTGGATGGGG	10391
rs576035906	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706540	TTGATGGCCAGGGGC[A/C]ACTATTCTACCTCAG	10391
rs576049195	in-del	-/TCAAAACCAATCTTGAAAACCAATC	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639780	TTTCTTTTACAGAGT[-/TCAAAACCAATCTTGAAAACCAATC]TCAAAACCAATATGT	10391
rs576062780	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68663461	TACGTGCTTTCTTCC[A/T]GGAAACACACACACA	10391
rs576084009	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701997	CCTGTAATCCCAACA[A/C]TTTGGGAGGCTGAGG	10391
rs576106396	snp	C/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68656979	CCTAGGGTCCAGTCC[C/G]CCCGATCCCCAGTTT	10391
rs576115743	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68559246	TGGGCTTTGTTTTGC[A/G]AAGAGCATTTGCATA	10391
rs576119307	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68572935	CTGTGCCCAGGTCTG[C/T]GGCTCCTTCTCCCTG	10391
rs576124651	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662867	TATATTTTATGCCAG[C/T]AAATGATAAGACAGA	10391
rs576168403	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68682306	GAAGAGACCAGCACC[A/G]TGGAGACCAATTAGA	10391
rs576172388	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68680797	CAATGACCTGTACTT[C/T]GTAAGGTTATTGTGC	10391
rs576184315	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68621887	TCAGCCTCCCAAGGA[A/G]CTGGGACTATAGGCA	10391
rs576189042	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68636490	ATCCCAGCCCTGCCT[A/G]TTCCCACTTGGCTTA	10391
rs576189094	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68629113	GGATCATGCTGGGGA[A/G]TGCCGAATGTATCTT	10391
rs576202833	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68558456	CACTGCAGCCTCAGT[A/G]ACCTCCCATGATTAA	10391
rs576221104	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68654720	CACTTAGCACGTAGC[C/T]TGGCCCATAGTACGT	10391
rs576222003	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68627828	GCCCCCTTCCTGCCC[C/T]GCACACCCTGGTGTA	10391
rs576235754	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68697198	TGGATTGTTGGATGG[A/T]TGGATGGATGGATTG	10391
rs576268931	snp	C/G	0.00318978	0.0398085	intron-variant	CORO2B	GRCh38.p7	15:68675241	ATGCTCTGGAATTCC[C/G]CTTGCGGCAGCTGCC	10391
rs576275734	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68685922	GAGAAAAAGAGTAGG[A/G]AGGGAGGGTCTCCAA	10391
rs576279180	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627392	GACCTTCAAGTGCAG[A/G]TGGGTCCCCAGGAAG	10391
rs576282646	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726911	TCTACCCAGCACCAG[C/T]AGTGCCGATGTGCCA	10391
rs576316667	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578814	CGGACCCGGGCGCCC[A/G]TCCGGACTCCGGGAG	10391
rs576318301	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671610	GTCATCTGAAGGCTC[A/G]ACTGGGGAATATACA	10391
rs576343529	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726305	AGCAAGAGGGGAAGC[A/G]GGATCCCAGCTAGAC	10391
rs576390220	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68574503	TAGCACTCGGTACAG[A/G]GCCTGGGCAGATGCT	10391
rs576415959	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68623272	GGCTCTTTTAAGCCC[A/G]GGCCCATGCTGCCTC	10391
rs576446103	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68715797	GCAGAAACCCAGAGA[A/G]GGCTCTGGGATTGAC	10391
rs576455720	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68614239	TCTTTATTGTTAAAT[A/G]AGTTACATGTAAGTC	10391
rs576470305	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68669759	AGAAATAAACCAAAT[A/C]AGAAAAAATAAATAA	10391
rs576498346	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68703430	TGCTGGGATTACAGG[C/T]GTGAGCCACCTCGCC	10391
rs576522294	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68627211	TGTTTTACTTTATGT[C/G]TGTGTATTCATTATT	10391
rs576532988	snp	G/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68676818	GCTCTGTCACCCAGG[G/T]TGGAGTACAGTGGCA	10391
rs576626644	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68713137	GGAGGCCCAAGACAG[A/C]TCAGTTAAGGAGGCA	10391
rs576634396	snp	A/C	1.6659e-05	0.00288604	intron-variant	CORO2B	GRCh38.p7	15:68719366	CTGGACCATCACCTG[A/C]CAGTCCATGGGATCG	10391
rs576634963	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68595141	GCATTCGAGGCCAGA[A/G]AACTGGCTGAGTGGC	10391
rs576642219	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589034	TAGAGACCCTGAGTC[G/T]GCCTTCCTGCCTTAC	10391
rs576643228	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68642161	CCTGCTTCAGCCTCC[C/T]GACCAGCTGGGATTA	10391
rs576662888	in-del	-/AG	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630523	CTTTGCTGTGGGGGC[-/AG]AAAGACCTCATGGGG	10391
rs576697015	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68652807	CCTTTAAGACTGCAC[A/G]GCCCACAAGTAGCAG	10391
rs576717598	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68601981	TGGCGGAAGGCAGAA[C/G]GCAGAAGGCCAAACA	10391
rs576729566	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588412	AATAATCTGGCTATA[A/C]AAATGTGGTGTCCTG	10391
rs576733874	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701898	CCCCTAAGAACTCCA[C/T]AGACATTAACTGTTA	10391
rs576767660	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68592738	TGTGTACTGTACAGT[A/G]TGTACGGAATGTACA	10391
rs576768279	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68587821	TAACTTTTACAGTGT[C/T]CCCACAGCCAGTCAG	10391
rs576786004	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68701544	AGGCTGGAGTGCAGT[A/G]GCGCGATCTCGACTC	10391
rs576818891	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68609874	GGGGTAGGGGAGCAC[A/G]AAGCGGTCTGGTTCA	10391
rs576854790	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68682387	GGAGCAGATGTAAAG[A/G]CGTTTGTGGGGATTA	10391
rs576902747	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68721423	TAAGAATGGTCATAC[G/T]GGCTGGGCGCCGTAG	10391
rs576905244	in-del	-/TGGA	0.0482946	0.147699	intron-variant	CORO2B	GRCh38.p7	15:68697214	GGATGGATGGATTGT[-/TGGA]TGGATGGATGGATGG	10391
rs576908537	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68579511	GGCCAACATCCCTCC[A/G]CGCCCGGCCCAACCC	10391
rs576919576	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68682566	GGACTCCCTAGATGC[G/T]GTGCTGAGGACTGCT	10391
rs576923325	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68627354	CAGGGCAACTTGCCC[C/T]CAGTGCCTGAGAGTG	10391
rs576965017	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68706683	GACAAGGGTAGCCGG[C/T]AGACATGAGAAAAGA	10391
rs576972737	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68576525	TCAGGATGACAATCT[C/G]GGATTTGAAATCTCT	10391
rs576987714	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578726	GGCGCCGCCCGTTCT[C/T]CCAGCCGGCAGGTGC	10391
rs577001745	snp	G/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68627033	CCACTGCCAAGTGGG[G/T]ATCCTTAGCAAGGTA	10391
rs577013270	snp	C/T	0.00279162	0.0372561	intron-variant	CORO2B	GRCh38.p7	15:68572069	TCTGGCCCAGGGGCA[C/T]CTGGGAAGGGGCTGT	10391
rs577023282	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68641556	CAGGCACAGAAACTG[C/T]GGGCCGCTGAGCGCT	10391
rs577030700	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68668551	GGTCAAGTAAAGAGC[A/G]TGCGGAAGAGTAGTG	10391
rs577039421	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68633486	TTGAATTGTTTCCAA[A/C]GTCCAAGAGGAAATG	10391
rs577066364	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68681152	CAGAAGGAGGAGGTT[A/G]CAGTGAGCTGAGATC	10391
rs577085272	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68648282	AGGTTGCAGTGGGCG[A/G]GATTGCGCTACTGCA	10391
rs577086846	snp	A/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641250	AGAACATGCCTGCTC[A/T]CCCCGAGCCTGAGCG	10391
rs577107664	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68585531	CACAGGTTGAATGAA[C/T]GGGTGGGGAGCAGGG	10391
rs577135443	snp	A/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68684339	CTCTTTGGAAGGCTT[A/T]TGTTTACTTGATTAA	10391
rs577138249	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68675175	GGCAGCCATGATGGC[A/G]AAAATACTTCTAGTC	10391
rs577190588	snp	C/G	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68581405	GATGCAGGAAAGGCA[C/G]TGGGGACTGCTTTGC	10391
rs577196125	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68596692	TGGAGCCAGGGCAGA[A/G]GCAGCAGGCACAGGG	10391
rs577203426	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68674660	AAAGGCTCGTGGGCA[A/G]TGGCTTCTCCGTGGA	10391
rs577226640	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68580765	GTAATGGATGGGCCC[A/G]GCTAGAGAGAGAAAG	10391
rs577260852	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68676740	CTCAGGAGGTCTAGA[A/G]GTGGCCCAAGATCTG	10391
rs577263152	snp	A/G	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68622615	CTACTCATTAGAAAC[A/G]GAAGCAGCTCAGCCC	10391
rs577267934	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68676011	TAATGCTAGGAGGAG[A/G]AATTGATTAGGGAAG	10391
rs577303906	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68691783	CTGTTCTGAATAGGT[A/T]CCGGTGATGTTGCCT	10391
rs577320475	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68714947	GAATTTGAGATACCC[A/G]CCAGGAGATCCTTGG	10391
rs577345815	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68622081	ATTTGACCTTCTGAG[G/T]CTTGGTTTTCCATCT	10391
rs577363678	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68588153	CCCACTCCTTTCCTC[C/T]TCCTCACCAGTATTT	10391
rs577378577	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68697603	GCAGCAGTGAAGGCA[A/G]TGCCCTTGGGAGCAG	10391
rs577387098	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634459	TTCACTGGATCCTCA[C/T]AACTATCCTAGGAAA	10391
rs577391528	snp	A/G	0.00159617	0.0282053	intron-variant	CORO2B	GRCh38.p7	15:68560591	GGCCTGAGCCACCGC[A/G]CCCAGCCTGCAGGTT	10391
rs577427616	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68566970	AATGACTCAGACTGG[A/C]TGATCCCCACTCTCC	10391
rs577465918	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68663435	AGAATTTAAATGGAT[A/G]GTTGAAGAGGTACGT	10391
rs577472589	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68659311	CCCAAAACTTAACTC[C/T]GCTGACCAGAAGCCT	10391
rs577473410	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68600525	GTCGGAAAGACAAAG[A/C]GGTCTTTGTTAACAG	10391
rs577492035	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68594504	GTGAACACTAATTCC[C/T]TGGGCAGGGTGGTCC	10391
rs577509449	snp	A/G/T			intron-variant	CORO2B	GRCh38.p7	15:68659950	CCTCATCTTCATGCT[A/G/T]AGTAGGCTGAAGGGG	10391
rs577529938	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68662811	GATCTGAAAGTGTGT[A/G]TATGTTTTGATAAAT	10391
rs577531661	snp	A/C	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68677708	TGCCAGCCCCTGTCC[A/C]TTCTGCAGATAAAAC	10391
rs577545555	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641395	CACCACAGATGCCTC[C/T]TTCCTGTGTCTACAC	10391
rs577579608	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68593795	GGACGCATTGCACCA[C/T]GCAAAGGTCCCATTG	10391
rs577582497	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68643390	CTGGGGAGGGGAAAG[C/G]GCAGTGACCCACCAG	10391
rs577610734	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	CORO2B	GRCh38.p7	15:68728179	ACCGCTATTCAATAG[A/C]TGCTGCCCCGTGTTG	10391
rs577618682	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727712	ATTTCTGGAGCTTTT[C/T]TTTTTCCTTCCCCAT	10391
rs577645442	snp	A/G	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68609558	GGGGCCTTCCCTCCC[A/G]AATCCACATCTCTTT	10391
rs577672011	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68603069	CTGTCAACGGTCTGT[C/T]AGGATAGGAGGTGAG	10391
rs577672883	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68637382	GTGTCCACCTTTCCC[A/G]GGTGGAGGGGGAACA	10391
rs577680403	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68647357	ATAGACAAAGTATTC[C/T]TGTGAAGAATATATA	10391
rs577734442	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68707114	TACAAGCGCGCGCCA[C/T]CACGCCCAGCTGCCG	10391
rs577742085	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68613032	ATGGGACTCCCCTCT[C/T]TCACTTCACCAAAAC	10391
rs577754344	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68602236	TGACTGGCTTTATTC[C/T]GGGGAATGACACTAG	10391
rs577759770	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68609897	CTGGTTCAGTACACT[A/G]GCTTGACCTGGAATC	10391
rs577791062	snp	C/T	0.000798403	0.0199641	intron-variant	CORO2B	GRCh38.p7	15:68609365	ACACCAGGCTGTTAG[C/T]GACCATCTTATTTCT	10391
rs577805684	snp	A/G	4.12074e-05	0.00453894	missense	CORO2B	GRCh38.p7	15:68710847	GGCACCCCACCACCA[A/G]CAACATCCTGTTCAG	10391
rs577812966	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68656131	GCCTTCCTCATGTCC[C/T]TGACTGCTGCCCACC	10391
rs577813907	snp	C/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68617160	AACAACATTGGCTTT[C/T]GTGGGCTCCAGGGAA	10391
rs577817795	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68710086	CATCCTCCTCTCTGC[A/G]GATCATCTTTTTCTG	10391
rs577819737	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68717219	CTTGGGAGGCTAAGG[C/T]AGGAGAATCGCTTGA	10391
rs577834541	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68557708	TTTGAAGCACAGAGA[G/T]GTTAAGTAAATGCCC	10391
rs577847828	snp	C/T	0.00438332	0.0466095	intron-variant	CORO2B	GRCh38.p7	15:68623379	TGCTTTGCACCACCA[C/T]TGGAAGGTCATGTGG	10391
rs577896787	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68702744	ATGGAAATCTTGGAG[C/T]CAATGATTGTGTACT	10391
rs577903731	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68573919	AGGAAGGCTTTCTGG[A/G]GGAGGCGATACCTAA	10391
rs577903813	snp	C/T	0.00199481	0.0315187	intron-variant	CORO2B	GRCh38.p7	15:68708712	TGAGACAGAGTCTCG[C/T]TCTGTTGCCCAGGAT	10391
rs577939345	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616257	CCCTGCCTCTTCCCC[A/G]TCACCTCAGATGCAC	10391
rs577952945	snp	A/T	0.00119737	0.0244387	intron-variant	CORO2B	GRCh38.p7	15:68604515	GTGTGGTTTTTTTTT[A/T]AAAAGGCGACTTTAT	10391
rs577959886	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68589716	TGATTCAAAAGTGGG[A/G]AATGGGAGAAAGTTC	10391
rs578071054	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68674421	GAATGCCCCAGGTGA[C/T]TGTGTGCCCTGGGTC	10391
rs578074462	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68644383	TTCTTATAAATGACA[C/T]AGGAAGATCAGAGAC	10391
rs578151171	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68617531	TGTGCGTGTGTGTAT[A/G]TGTGTGTCTGTGACT	10391
rs578154005	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68665590	GTTGAGTCTAAATAT[C/T]CATGATCATAGTTTA	10391
rs578165987	snp	C/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68583252	TCTCTAGGGCCCCTA[C/T]AGAGTCACCCATAGG	10391
rs578166946	snp	C/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68568377	CACAGTGCCTAGACA[C/G]AAGTGCTGGCTACCA	10391
rs578198395	snp	A/G	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68678137	ACTTGTACAGCACCC[A/G]TGCCACTGGCTGCTG	10391
rs578215197	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630507	TTAAAATAGCAAAGT[G/T]CTTTGCTGTGGGGGC	10391
rs578231339	snp	A/C	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68664655	CTGTCTCAAAAAAAA[A/C]CCAAAAACCAAAAAA	10391
rs578246978	snp	G/T	0.000399281	0.0141238	intron-variant	CORO2B	GRCh38.p7	15:68671444	ATCAAAATCTGAGAT[G/T]ATAATGCCTGTTCTG	10391
rs745306529	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68672454	GCCTGGCTAATTTTT[G/T]TGTGTGTACAGATGG	10391
rs745312690	snp	A/C	1.8739e-05	0.00306091	intron-variant	CORO2B	GRCh38.p7	15:68645151	CTTGTCTCTCCTGGC[A/C]CCTCACAGATGTCCT	10391
rs745317438	snp	C/G	1.65135e-05	0.00287341	intron-variant	CORO2B	GRCh38.p7	15:68714552	GAGACCAGCTCTTCT[C/G]CCTCAGGAGGACCTC	10391
rs745350124	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702338	CTTTCATGCATCCAG[C/T]GCCACAACGACCACT	10391
rs745363992	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68715542	GGCAGCTTGCCAGCA[G/T]GTGCTCTGCGTCTGC	10391
rs745395571	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68683929	GGCAGGACTGTGCTG[A/G]GATGACAACAGCTCT	10391
rs745412629	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603063	ATGGGTCTGTCAACG[A/G]TCTGTTAGGATAGGA	10391
rs745419187	snp	C/T	1.65154e-05	0.00287358	synonymous-codon	CORO2B	GRCh38.p7	15:68645219	CTACGGGAAGGTGGC[C/T]AACCGGGAGCACTGC	10391
rs745441001	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68714224	TTCAAGGAACAATGT[C/T]GGCCACACCTGCAAG	10391
rs745493216	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68628914	GGCAAGCTGGGGAAA[G/T]GGCAGGATGAGAATG	10391
rs745504334	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68673838	CGAGACTCCGTCTAA[-/AA]AAAAAAAAAAAAAAA	10391
rs745541847	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591814	GGGTTGAGAACATAG[A/G]AGGGGGCAGAGGACC	10391
rs745585535	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68620158	CTCAGATGATCCACC[C/T]GCCTTGGCCTCCCAA	10391
rs745600529	snp	A/T			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632119	CAGATTCCCGTTATC[A/T]TGACTGCTGCAGCGG	10391
rs745603407	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68636561	GGGTGGCGAGGAGGA[A/G]TTCCAATTTCCTGGG	10391
rs745619857	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68608709	CCTGCATCCTGAATG[A/G]TTGGAGCCTCATGGC	10391
rs745672565	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68690295	CCACCACTGCCTAGA[A/G]CCACAATCCCTGTCC	10391
rs745679684	snp	A/G	2.55653e-05	0.00357519	intron-variant	CORO2B	GRCh38.p7	15:68710919	GGTGGAGAGGGATTG[A/G]GGAAGAGAAAGGGGC	10391
rs745703153	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68663593	TGAACTTAATCAAAA[-/T]TAAAAACTTTTGCTC	10391
rs745704108	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68720243	GACTGAGCAAGTCTA[C/T]TGACCTTTATAAGTC	10391
rs745704254	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68711055	GCAACTCCTGTGCAC[C/G]CTGTCATTCCTGGGG	10391
rs745705361	in-del	-/AAAAA			intron-variant	CORO2B	GRCh38.p7	15:68603364	AATAATTATTATCTT[-/AAAAA]AACACACTTGCTAAT	10391
rs745709052	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648606	AGTGAGCCAAGATTG[C/T]GCCAGTGCACTCCAG	10391
rs745726973	in-del	-/CAAG			intron-variant	CORO2B	GRCh38.p7	15:68690921	GGCCTCCCAAAGTGC[-/CAAG]CAAGTGGGATTACAG	10391
rs745731274	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68566235	TGATGTGTTTTGAGT[C/G]CTTACTCTGTGCCAG	10391
rs745770183	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68681128	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGAAGG	10391
rs745792480	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68586877	GGCCCTCCTGGCTCT[C/T]AGGCAGGAGGGAGAA	10391
rs745793415	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68642225	AATATGGGAGTAGAT[C/G]GAAGTGGCACAGAGA	10391
rs745802535	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68599483	CGTCATAGCTTCAGC[C/T]ATATAAGATGCATTC	10391
rs745804200	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600047	GCAGAGGGAGTAGAG[A/G]CAGTTTCTGTGTGTA	10391
rs745833760	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68714820	CCCTCAAGTCTGACA[C/T]CCATTCTTACTCAAG	10391
rs745839518	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68667624	TGAGGAGTGGGACGG[A/G]TGAGGCCCTGTGGAT	10391
rs745902750	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68687821	CAAGAGAAGACCAAA[C/T]TCACTTTTATAACAA	10391
rs745905039	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68644848	CTCTATCACATGATA[C/G]GTTCCTGGGTAGTAA	10391
rs745942195	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722635	AATTTTGAGAACTTG[A/G]AAGACGCAAGAGTGT	10391
rs745944390	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68598617	CCTGCCCTGGAGCCC[A/G]CTTGGCCTTGAACGC	10391
rs746014438	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68706163	GCCAGCCTGCTCCAC[A/G]CGAGCCAGGCTGACC	10391
rs746017162	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68687047	CATCTTTCTCATGTG[A/G]ACTCAATATGGATTC	10391
rs746017268	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68575000	TGTGTACCGTATCCC[C/T]TCAGGCTACCCCACC	10391
rs746025019	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68564452	GGGACTACAGGAGCG[C/T]GCCACTACAACCGGC	10391
rs746028747	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68571265	CAGTACATGTAAATA[C/T]AGATGCAACCAGCAT	10391
rs746037370	in-del	-/AAC			intron-variant	CORO2B	GRCh38.p7	15:68707217	AGGAACACAAATCCA[-/AAC]AACAGGTGGCATTTT	10391
rs746058660	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68623969	GCCCAGCCCTCCTCA[C/G]CTCAACCTCCAACAA	10391
rs746068690	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68635071	TTCAGGTGATTCTGA[C/G]GCAGATGACCTGGGG	10391
rs746076011	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68595941	TGAGGGAAGGAGCAG[C/T]GTGAGCAGAGGCCAG	10391
rs746089132	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68659155	TACTCAGTTCCTCCA[G/T]TAGGAGGGAATTGCT	10391
rs746097770	snp	G/T			downstream-variant-500B	CORO2B	GRCh38.p7	15:68727999	AATAATTCTTTGCTG[G/T]GGGGGCTGCCCTGTA	10391
rs746109872	in-del	-/AT			intron-variant	CORO2B	GRCh38.p7	15:68565386	TATATTCAAGTGCAT[-/AT]ATATATATATATTCA	10391
rs746110594	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606075	GAAGCCTCGTTTACT[A/G]AAAGTCATGGTGGCA	10391
rs746116982	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68717950	CATTGTTGTCCTCCT[C/T]GAACCAGCCAAGGAA	10391
rs746142868	snp	A/G	1.68043e-05	0.0028986	intron-variant	CORO2B	GRCh38.p7	15:68645367	CTGGAGCAGGTAGGT[A/G]GCCCCTACCTTCACT	10391
rs746145034	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68634231	AGCCCTTATTGAGCA[C/G]TTGGTGTTTGCATGA	10391
rs746146671	snp	A/G	6.59859e-05	0.00574357	synonymous-codon	CORO2B	GRCh38.p7	15:68715298	CCGCTCCCCAGCCCC[A/G]CAGAAAGGCCTAGGT	10391
rs746161427	snp	A/G	1.65031e-05	0.00287251	missense	CORO2B	GRCh38.p7	15:68695168	AACCCAACTACCCCA[A/G]GGTCTGCGGCCACCA	10391
rs746213865	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68695337	CTCTTCCTACCCTCC[C/G]CTCCTCCACCCTTTG	10391
rs746234301	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68665072	TCTGAGATTATAAAG[A/G]AGTAACCTTTTTACT	10391
rs746239842	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68663832	AGTAGTTTCAATTAG[C/T]ATTCTTATTAAGACA	10391
rs746271192	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68610556	GTTCTCCCATCCTTC[A/C]ATCACAAAGCCCCTC	10391
rs746316316	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68559382	GACATCCATTTTAGA[A/G]GTTCTGGTCAATCGT	10391
rs746343721	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68670169	GATGGCAAAGCAGAA[A/G]TACTTAGTGGTTTGT	10391
rs746349588	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68614322	ATATTGCAAAAGGAA[A/G]GTGCCGTATTATCAC	10391
rs746352389	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68587804	CAGGGAAGGAAGGGA[G/T]GTAACTTTTACAGTG	10391
rs746369349	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68602186	ATTCGCAAGGACCAC[A/G]GACTTGGTCCTGAAG	10391
rs746389501	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68613146	GTCTTACATCCAGCT[C/T]ACACCCAGTTGGCCA	10391
rs746420082	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68723925	AAAAAATAAAAGTAG[A/G]CCGGGGTGGTGGCTC	10391
rs746440309	snp	G/T	3.30101e-05	0.00406251	missense	CORO2B	GRCh38.p7	15:68719495	CAAAGAAAAGAAGAG[G/T]GTTGTGGTCAACGGA	10391
rs746462968	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68655018	GACTGAGGTGGCCAT[A/G]CCAGGCTGGGTGCCT	10391
rs746470786	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68632849	TGCCCGCCTTGGTCC[C/T]CCTAAGTGCTGGGAT	10391
rs746489981	in-del	-/A			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630925	GAAAGAACTTTTCTT[-/A]ATGTCTCTCTCCTCT	10391
rs746505987	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68704578	CCCACGTGCAGGGAC[A/G]GTTGGTTTTGTAGCT	10391
rs746509404	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68674321	GGACGGTGGGTAGTA[C/T]ATATTCTCTGCACAC	10391
rs746531153	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68660222	TTGGACCCTTCTGCC[A/T]GATTGTCTAATGTCA	10391
rs746550278	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68593083	AGACAGAGAGAGGAA[A/G]TTGGGCCAAACTCAT	10391
rs746564974	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68580193	AAGAACCAATAACAT[C/T]AAGGGTGTGAACCCA	10391
rs746601473	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68567056	GTGAAGTGGGTATCA[A/T]AATAAGACCTATAGC	10391
rs746625589	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68621571	AACTGTGGCTCTGTC[-/T]TCATAACTCTGCCTT	10391
rs746643745	snp	A/G	3.29984e-05	0.00406179	intron-variant	CORO2B	GRCh38.p7	15:68719137	TCTTCTGCTCCTCCC[A/G]CTGTAGTCAGATTCC	10391
rs746648381	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68609007	TCAAGGTGCAGCAGA[A/G]AGGAAATCAACTTGG	10391
rs746657449	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68664151	TTTATGAATGTACAC[A/G]TGCAAAAATTCAATG	10391
rs746663746	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68610363	AGGGCTGGGGGCTGG[C/T]TTGGGCCCTGCATGC	10391
rs746689841	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68581231	ATACCCAGCCCCCAA[C/G]AAACCCTCCATGTCG	10391
rs746706728	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68650013	CTGAGGACCAGCGAT[A/G]CAAAGTAATATTTAA	10391
rs746715468	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68638641	GGAGGAGAAGATATG[A/T]GTTGTATTGGAAAGA	10391
rs746747208	snp	A/G	5.83584e-05	0.00540146	intron-variant	CORO2B	GRCh38.p7	15:68710932	TGGGGAAGAGAAAGG[A/G]GCCTTTTGGGTACCC	10391
rs746752522	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68557543	ACATCTGGAAAATGG[C/T]AGTGCAGGGATGGAA	10391
rs746761396	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68627274	TCAGAAATGACTAAG[A/G]CATCATCCCAACCAT	10391
rs746793757	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682055	CCAGTCCCATGCCCC[A/G]TCCCTGGATAGCAGA	10391
rs746807430	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68644723	CCACTCCTGCTGTGG[G/T]CCCTGTCCTCAATCT	10391
rs746815902	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722006	AGTCCTCCCACTTTC[A/G]CCTCCCAATGTGCTG	10391
rs746816183	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68681272	AGGAAGACCACAAGA[C/T]GTGAAGTGCACTAAA	10391
rs746819317	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68583875	GCTCCCGGGTGGGAG[C/G]CCACTTGCGGGTGGG	10391
rs746838857	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68682599	GCTCAGGCAGGACTC[-/AG]TGAGCGATTGGTAAT	10391
rs746843626	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68637918	TAGAAAATGCACCCG[C/T]TGGCCACAATAAATC	10391
rs746876555	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68710888	GACTACAAGGTATGC[A/C]GTGGGCAGGCAGCTG	10391
rs746880549	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68699729	CCTCTCCTGGAGGAC[A/G]TGCTCTGGGACCCTA	10391
rs746880707	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68589399	CCAGGTATAGACATA[C/T]AAGATTTGGCAGGAT	10391
rs746968279	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68588225	CACTTCTCCCCTGCT[A/G]TAGTCCTTATTTCAG	10391
rs746987292	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68628494	CTAAGTGTGAAATAC[A/T]TTAAAATATGTAACA	10391
rs747062829	in-del	-/CTC	8.29442e-05	0.00643935	intron-variant	CORO2B	GRCh38.p7	15:68695107	GGCCATCAAACTAAT[-/CTC]CTTCTCTCTCTCTCT	10391
rs747064429	snp	C/T	6.62921e-05	0.00575688	intron-variant	CORO2B	GRCh38.p7	15:68715320	GGCCTAGGTAAGTGG[C/T]CCCGAGGCTGCCACA	10391
rs747117056	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68636426	GCTTGCATTGGGTGG[C/T]GGATGCATGCTGCGT	10391
rs747129793	in-del	-/GAGA			intron-variant	CORO2B	GRCh38.p7	15:68700804	GGGCCAGCAGCCGCG[-/GAGA]GAGAGAGAGGTTTCT	10391
rs747153926	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68564560	CAAGCGATTGGCCTG[C/T]CTTGGCCTCCTACAG	10391
rs747161660	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68695472	ATCTGTGTTTTCAGT[A/G]TGATTGAGCTTGGAG	10391
rs747161679	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68707919	GGTATTCTGGGCCCC[C/T]TATACATCACTCCCT	10391
rs747169356	snp	A/G	3.85587e-05	0.00439066	intron-variant	CORO2B	GRCh38.p7	15:68718663	TGAGACGCAGTTTCT[A/G]GGACCCCATGGAGCC	10391
rs747203345	snp	G/T	1.65023e-05	0.00287244	missense	CORO2B	GRCh38.p7	15:68695186	TCTGCGGCCACCAGG[G/T]CAATGTGCTGGATAT	10391
rs747211198	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68613352	GGGCTTCAAAAATCC[A/G]TGTGATGGTAGAAGC	10391
rs747214567	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68719985	GTTTATGAAGGTGCT[C/T]TCTGTACCACTTGGA	10391
rs747251169	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68636232	CAGCATGGAATCTGG[C/G]GGCCTCAGAAGACTT	10391
rs747257885	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597875	TGTGGTGGTCCAGGC[A/G]AGAGGCCTGAGCTGA	10391
rs747293244	snp	C/T	0.000123232	0.00784863	intron-variant	CORO2B	GRCh38.p7	15:68710685	CCTCTCATCAAGGGA[C/T]TTCTTGGCCGTGTCC	10391
rs747301043	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68624785	GCAACCTCCATCTCC[C/T]GATTCTCTTGCCTCA	10391
rs747317778	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68713849	ATGGGTGTATCTTTT[C/T]GGGACCACCATTCAT	10391
rs747327128	snp	A/G	1.65124e-05	0.00287331	synonymous-codon	CORO2B	GRCh38.p7	15:68719501	AAAGAAGAGTGTTGT[A/G]GTCAACGGAATAGAT	10391
rs747338664	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68654723	TTAGCACGTAGCCTG[G/T]CCCATAGTACGTGCT	10391
rs747340228	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68560879	AGCAGAACCGCAGCT[C/G]TCCTCACGATCTTGT	10391
rs747361163	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68690913	ACCTGCCTTGGCCTC[C/T]CAAAGTGCCAAGTGG	10391
rs747365232	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68684141	GCCCACTTCAGAAAT[C/T]CTGCCAGCTCTAGAG	10391
rs747367508	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68653973	GATCTTTCCTCAATC[A/G]TTCTTTGTTCTTCAA	10391
rs747390017	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68571021	TTCTTTTGGAAGAAA[G/T]TGCGAAGGAAACAGA	10391
rs747417957	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68725031	TTCTGTATCCTGAGC[C/T]TCCTTAAGAAGAGAA	10391
rs747422826	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68685019	GAAAGTGATGATAGG[C/G]GTGGCCCATGAAAAA	10391
rs747427477	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68586579	GTGACATCATGGCAT[A/G]GGTTACTGTTATCAT	10391
rs747428560	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68667036	AAGACCCTCGACAAA[C/T]AGGCCCTAGGCTTCC	10391
rs747429772	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68672951	AATGGGGGGTACCAG[C/G]GTGTGGGGTATGGGT	10391
rs747431771	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68696789	TGAGCTGGTGAGGAG[A/G]GCCTGGTGTTCCCAG	10391
rs747467630	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68603815	CGAAATAAATATCTG[C/T]TGTTTAAGCCCCCAG	10391
rs747486665	snp	C/T	1.73646e-05	0.00294652	intron-variant	CORO2B	GRCh38.p7	15:68719600	CTGGAAGAGCAAGAC[C/T]TTTACATTTCAATTA	10391
rs747488747	snp	C/T			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632211	TTGGGCGCTATTCAT[C/T]CACACGGCCCATCTG	10391
rs747541173	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725745	CTGGGGGAATGTGAG[A/G]GCACGGGCGGCAGGC	10391
rs747548634	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591875	AGCATGGCGAGAAGA[A/G]CACTGGAATGGGATT	10391
rs747584283	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68681385	ACAAGGAATGCAGGG[A/G]GGGGGCCAGTGAGGA	10391
rs747585201	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68572493	TGAAAACAACTCCTT[C/T]ATATCTGTTTTGCAT	10391
rs747598174	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68651650	GAGCAAACAGCAGGC[C/T]GCAGAGAATTGTCTC	10391
rs747620702	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68685242	TCGGGAGACAGTCTT[A/G]CTTTGTTGCCCAGGC	10391
rs747660767	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694089	GATCTGCCCGCCTTG[A/G]CCTCCCAAAGTGCTG	10391
rs747662221	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68582535	CTTTGTATAATTTTC[G/T]TGTTCTGTTCCATCT	10391
rs747685732	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68650159	TGATCACCCGAGGTC[A/T]GGAGTTCAAGACCAG	10391
rs747709982	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68686446	GCAGACAGCCAAGTG[C/T]AGATGATAGCTCCTC	10391
rs747783046	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68569485	CATTTCTTTTTGACA[C/T]GGAATAATATTGCAT	10391
rs747788079	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68568434	ACTATTGCCCTTTAC[C/T]CTCTGAGAGGTTGTC	10391
rs747801690	snp	A/G	6.59881e-05	0.00574367	missense	CORO2B	GRCh38.p7	15:68719478	GTATTTAAGGCTCCC[A/G]TCAAAGAAAAGAAGA	10391
rs747807424	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68628779	TTATCCTGCCTCCTC[C/T]GGAGTCTACATGGAC	10391
rs747815373	in-del	-/ACA			intron-variant	CORO2B	GRCh38.p7	15:68715546	CTTGCCAGCATGTGC[-/ACA]TCTGCGTCTGCACTC	10391
rs747822056	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68601359	CACCCGTCCCTGGGC[C/G]TCATTCAGCCAGCAT	10391
rs747831701	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68722074	TTGTTTTTAAAAGAA[C/T]TCTACTCTTTGAAGA	10391
rs747851770	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68629691	GGAGGGTCAGTGACA[C/T]GAGCAGCCTCAGTAG	10391
rs747853339	snp	A/G	1.66849e-05	0.00288828	intron-variant	CORO2B	GRCh38.p7	15:68711738	TTTGAGATTGAAGGG[A/G]AAGGTATTGAGGGCT	10391
rs747870025	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68700232	GGCAAAGCTGCTGTG[C/T]GTGCCAGGCACTGTG	10391
rs747911282	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68717295	CTCCAACCTGGGCAA[C/T]AGAGCCAGACTCTGT	10391
rs747938598	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68670595	TATACAAAGAGCTCT[G/T]ATAAATTATTAAGAA	10391
rs747997987	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68698534	GCATCCCCGGCCACA[G/T]GAGCCAAGAGACTCT	10391
rs748000054	in-del	-/CCC			intron-variant	CORO2B	GRCh38.p7	15:68637745	GAGTTCTCCTGGGCT[-/CCC]CCCACATTACACAGC	10391
rs748014963	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68576999	CAAGGAGGTGGTGCC[A/G]TGAGAGGTGGGATGC	10391
rs748015092	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68563697	ATGTCAGAAATGAAA[C/T]TGGGGACAATACTAC	10391
rs748041379	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68699955	CTCAGGGTCCAACCT[A/G]GGTGCTGGGGGAAAG	10391
rs748042283	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68683552	TTCCAACAGTTACAG[-/T]TTTTGGTGCACCACC	10391
rs748044115	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68618365	GTAAATCATGTGCTA[C/T]GGAAAAGGAGCAAAA	10391
rs748058724	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68590728	GTCATTGACTGGACC[A/G]AGCCTGCTGGAAGGA	10391
rs748070983	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727343	TTTGATCTTGTACAC[A/G]TTTTCTTTTATTCCT	10391
rs748085512	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606148	TACCATGTTAGGTCA[A/G]AGGTGACTGCAAGAA	10391
rs748095887	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68626039	TTAATTGTTTCTAGC[C/T]TTCATCCAGAAATGC	10391
rs748098691	snp	C/G			downstream-variant-500B	CORO2B	GRCh38.p7	15:68728167	AACCACTGTTCTACC[C/G]CTATTCAATAGATGC	10391
rs748107199	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68575682	TTGCTCCTTCTCAAC[C/T]GCACTACTCCCCACC	10391
rs748183740	snp	C/T	1.70026e-05	0.00291565	missense	CORO2B	GRCh38.p7	15:68718805	TCCATGATCGTGCCC[C/T]GGAGGGTAAGTGGGG	10391
rs748197763	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68641788	GTAGTGCAGTGGTGC[A/G]ACTCAGCCCACTGCA	10391
rs748202463	snp	A/G	3.04521e-05	0.00390194	intron-variant	CORO2B	GRCh38.p7	15:68710695	AGGGACTTCTTGGCC[A/G]TGTCCACCCAGCCTG	10391
rs748209404	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68667375	TCCTTGCCATGTTTG[A/T]GGCAGGGGTATCGTG	10391
rs748209677	snp	A/G	3.92288e-05	0.00442864	missense	CORO2B	GRCh38.p7	15:68710774	GGGCTGAAGCGGAAC[A/G]TGACGGAGGCGCTCC	10391
rs748227595	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68665750	TTGATGATTGTATAC[C/T]AGAAAGCCATAAGTT	10391
rs748293713	snp	A/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616125	TTAAGTAATTGCCCA[A/G]GGACTGACTCTACGG	10391
rs748298635	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68599344	CTGAGTGGGAGGGAG[C/T]GTGTCGCGCCACAGA	10391
rs748303629	snp	A/G	4.97863e-05	0.00498906	missense	CORO2B	GRCh38.p7	15:68725862	TTCGAATGTTCTTCC[A/G]GCAGCAGGATGAGAT	10391
rs748336932	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68684259	AGCTTTCTCTAAAAG[A/G]CTCCTGTCAATATGT	10391
rs748343432	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68698327	GGGGGGACAAATTAG[A/G]CCAGGGCTCCTGGAA	10391
rs748358387	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603327	TATGCACAGATGAGC[A/G]AAAGTTGGCCTGTAA	10391
rs748405512	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68654865	TGAGCCTTGTCTTTG[G/T]CCTTCCTGCTACTGT	10391
rs748414949	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68571643	ATTACATTTTAAAAT[A/C]AAATTGTTTATATAG	10391
rs748416317	snp	C/T	1.67125e-05	0.00289067	intron-variant	CORO2B	GRCh38.p7	15:68714062	CCACGGGGAGGCCTG[C/T]TGGGTTTGGGCTAAA	10391
rs748431275	in-del	-/TC	0.00451635	0.0473051	intron-variant	CORO2B	GRCh38.p7	15:68695111	TCAAACTAATCTCCT[-/TC]TCTCTCTCTCTCTCT	10391
rs748459536	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654015	CTTGGTGCAATTTGC[A/G]TCTCAAAGCCCATGA	10391
rs748467956	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68632362	TAGCAGTGATAAAAC[A/G]CATTCAGCTCGGTCC	10391
rs748515365	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68562641	AACTGGATCACAGAA[A/G]AATCACAAGAGAAAT	10391
rs748517900	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595344	AGGAAGGGGGACATG[A/G]ATGTCCAGTTTACAT	10391
rs748520306	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68561639	ACATGCAGAGAAACA[C/T]GCACACACCCAGAGC	10391
rs748532033	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68656005	GCCTTGGCCAAGGCT[C/T]CTACCACTGGCCTTT	10391
rs748539635	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68685115	CCACTGCCCTCGGTA[C/T]TCCTTTACATGCTCA	10391
rs748547562	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68655155	TAATGAGGGAAGGCA[C/T]GTAAAGGTTTTACCA	10391
rs748609810	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68568380	AGTGCCTAGACACAA[A/G]TGCTGGCTACCATTT	10391
rs748613682	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726497	AAGCCTGCCTCACCC[A/G]ACGAGGACAGCGAGC	10391
rs748635407	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630969	ATCCTTCTCAGAAGC[C/T]CCCTAGTGGACTTCC	10391
rs748661297	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68605823	TCCACCTCCCGGGTT[C/T]AAGCAATTCTCCTGC	10391
rs748662371	snp	A/G	1.6486e-05	0.00287102	missense	CORO2B	GRCh38.p7	15:68714573	GGAGGACCTCTCCAT[A/G]CCCCTGATCGAAGAG	10391
rs748667279	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604942	AACATAGTGAAACCC[C/T]GTGTCTACTAAAAAC	10391
rs748675761	snp	C/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640236	CCTTGGCACTGGCCA[C/G]GTGGCCTCCTCACTG	10391
rs748685013	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68581433	TGCTGTCTACAAGCC[C/T]GCTGGTAGTAGCTCT	10391
rs748718564	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68559107	AATGCGCGAAGTGTG[G/T]CTGGGCGTTGCCAGG	10391
rs748760462	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68633113	GGAGCTGGTTGGTTT[A/G]GCTGTCACCATTGAG	10391
rs748766142	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601411	TGTGCCTTTCGGTAG[A/G]CACCGAGGATAAAAC	10391
rs748766503	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68612834	GGGAGTTCCCAGCAG[C/T]TGGGGAGAGAAAGGT	10391
rs748810483	snp	C/T	3.30387e-05	0.00406427	missense	CORO2B	GRCh38.p7	15:68695228	CCTTCATCGACAACA[C/T]CATTGCCTCGTGCTC	10391
rs748810589	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68569565	CTTAGTTGTGCCCAA[A/G]TTTTGGCAATTCTGA	10391
rs748812440	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68682236	TGGAAGATTCTGGAA[G/T]AGTTGCACAAGGAAA	10391
rs748866442	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68706794	AGCTCACTGCAGCCT[C/T]GTCTTCCTGGGCTCA	10391
rs748904383	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630663	ACCAAGACTGACTCA[A/G]GCTCTAGGATTTTCA	10391
rs748904697	in-del	-/TT			intron-variant	CORO2B	GRCh38.p7	15:68709462	TTTTTTTTTCGTGTT[-/TT]TTTTTTTTTTTTTTT	10391
rs748908795	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68589966	CCTCCACAGTGGCCC[A/G]TGACCCCCGGCTCTC	10391
rs748922154	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68561879	GGGAATGTCAATGAG[C/T]AGTAAAGGGGTGCCT	10391
rs748958441	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68602092	CACCTCTGAAAGGAT[A/C]TGCCTCGAATACTAT	10391
rs748968986	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68590857	TGTGGAGAGGAGAGG[A/C]CAGCCAAGCTTATTC	10391
rs748972712	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68712898	AACAGAGAACCCCCA[C/T]CTCCAATTCCCAAAT	10391
rs748993509	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68724654	AAAGCATTTAATTAA[A/G]TTTTTATAGAAACAA	10391
rs748994197	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68629765	ATTGAGAACCCTGAC[C/T]TCATGACTGGGACCC	10391
rs749017998	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68670904	TCTTAAAATTCATAA[C/G]AAAAGCATTTTTTTA	10391
rs749029914	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68646774	GCTCCTAGTGAACCA[C/T]ACAACATGTTAAGGA	10391
rs749040790	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641022	GGTTGTGGAGCCATC[A/G]ATCAACAGCAGCCCC	10391
rs749096966	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68648029	AAGATCCTGTCTCTC[-/AA]AAAAAAAAAAAAAAA	10391
rs749138004	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68658627	GAGCTGCTTAATGGC[C/T]CTGTGACCTTGGGCA	10391
rs749160410	snp	A/C			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577134	GCACATCTGCTACCC[A/C]AGAGATTTAGTAAGT	10391
rs749190683	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68720073	TATTTCGTTCCAGCC[C/T]ACACCCCCATTCCCT	10391
rs749203994	snp	C/T	1.77574e-05	0.00297966	intron-variant	CORO2B	GRCh38.p7	15:68718821	GGAGGGTAAGTGGGG[C/T]TGGGCTGGGCTCCAG	10391
rs749212338	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68636401	TAGAATAGACCGTGT[C/T]TCTGGCTGGGCTTGC	10391
rs749219377	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578240	CACTCAGTGGTAGTG[C/T]AGACAGTCCTAGGGC	10391
rs749255033	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564692	GATGATAGAGTCATT[A/G]TAAAGATAAAGAAAT	10391
rs749293733	in-del	-/TG			intron-variant	CORO2B	GRCh38.p7	15:68664354	TAACCTCTTAAAAAC[-/TG]TGAGAGTTATTGGCG	10391
rs749297362	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699637	GAACCGCATCTTACC[C/T]GGGTGTCCACCCCTC	10391
rs749302362	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648504	ACAAAAACAAAATTA[A/G]CCAGGTCTGGTGGCG	10391
rs749312795	snp	G/T	5.00576e-05	0.00500263	intron-variant	CORO2B	GRCh38.p7	15:68710914	AGCTGGGTGGAGAGG[G/T]ATTGGGGAAGAGAAA	10391
rs749318830	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68644074	CAACAAAAAAAACCA[A/G]CTACAAAGTATATCA	10391
rs749330785	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68628320	GTCCCTTCTTGCCTG[G/T]GTGACCTTGAGCAAG	10391
rs749358905	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68685607	TTTCAGGTGCTCCAG[G/T]AGGCAGGAGGCCCAG	10391
rs749361833	in-del	-/TG			intron-variant	CORO2B	GRCh38.p7	15:68619665	AATGCTGGGTGTAAA[-/TG]TGTGTGTGTGTGTGT	10391
rs749375300	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578071	GTTCTGCTCAGGTGC[C/T]TGGGAGGGAGACTCC	10391
rs749407413	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68676622	GAGTGCAGGTCTCAG[C/T]CGTGTTTCCCAAGTC	10391
rs749414520	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68716766	TCTGTGGCCAGAATG[A/G]GCCTGGCATGTTCTA	10391
rs749424731	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68686959	CAAGGCCTAGCACTT[G/T]GCACTCACTCATCAA	10391
rs749431571	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68572905	CTGGGAGGAGGCTGC[C/T]CTGGGGTTTCCTCAC	10391
rs749446902	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68698471	GCTCCAGGACCCCAG[C/T]TTGTAAACAAGACAT	10391
rs749451556	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595989	GTGCTCCCGAGCCAC[A/G]AGGGTGCCCAGTGAG	10391
rs749453690	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68605201	TCCTATGGCAGTGTC[A/G]TCCAAAGTTGTATAA	10391
rs749457768	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68655262	GAGAAAACGGTGCTG[A/G]AATTGAGACGGAGGC	10391
rs749462115	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68562762	GGTGGGTCACGAGGG[A/G]TCAGGAGATCGAAAC	10391
rs749472275	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727201	CTCGCATCCGTATAG[C/T]ACTTTAAAGTTTCTG	10391
rs749493485	snp	A/G/T	3.31638e-05	0.00407198	missense	CORO2B	GRCh38.p7	15:68725880	AGCAGGATGAGATTC[A/G/T]ACGGTTGAAAGAGGA	10391
rs749526605	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604115	ATTTGGCACAGAGCC[C/T]GGCACACAGTCAGCA	10391
rs749553110	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574117	TGCAAGAGCTGCTGG[A/G]GGAGAACAGACTGAG	10391
rs749555605	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68623026	GAAGCATAGCTGGGT[A/G]TGGTGGTGGGCACCT	10391
rs749606213	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68634034	GGAGCCTCGGCAGTG[A/G]CAGCTATGCCTGGCA	10391
rs749606267	snp	C/G/T	3.29702e-05	0.00406008	intron-variant	CORO2B	GRCh38.p7	15:68715189	CTACCTGCCACCTTC[C/G/T]TCAACTCCATCTCTC	10391
rs749627917	in-del	-/CCT	1.6476e-05	0.00287014	cds-indel	CORO2B	GRCh38.p7	15:68714609	TGATGGGCTCTCTGG[-/CCT]CCTGTTCCCCTTCTA	10391
rs749643461	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68705964	GGCTCACTCCACAGC[C/T]CCCCATGTGACTCTA	10391
rs749657342	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68676973	AGAGACAGGTTTCAC[A/T]GTGCTGCCCAGGCTG	10391
rs749683197	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68633757	CCTTTTACTCTAACA[A/G]AGATACTACAACGGA	10391
rs749684348	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68704785	GGCTCTGACCCAGGG[A/G]CCTGTAAAGGGGACA	10391
rs749689866	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68594900	TGGTTCTACTCTGGG[C/T]TTTGCCTCTATCATG	10391
rs749693049	snp	A/G	0.000199154	0.00997683	missense	CORO2B	GRCh38.p7	15:68645343	GGCGGCTCCTTCCTC[A/G]TCATCCCCCTGGAGC	10391
rs749705510	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68685690	CATTGAAATCAATCC[A/G]GGAAACCCATTAAAA	10391
rs749730076	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68717820	GGAGGAGAGGCAGAG[C/G]CTTAACTCATATTCA	10391
rs749732567	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68583968	CCAGATATCCAGCAT[G/T]CTCATGCTGGGAGGT	10391
rs749733068	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68705235	TTGAGGTCAGGAGTT[C/G]GAGACCAGCCTGGCC	10391
rs749736967	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68563300	TGAGACCAGCTTGGG[C/T]AATATAGTGAGACTA	10391
rs749740138	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68568595	AAACATAATAGTACC[A/T]ATCCCTTATGTCAAT	10391
rs749759164	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68694360	GCTAAAAAGTAGACA[C/T]TGCTATTCTCATTTT	10391
rs749782635	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648328	CAGAACAAGATTCCA[A/G]CTAAAAAAAAAAAAA	10391
rs749790226	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68612068	GAGCCACTGCACCCG[G/T]CCTCAACTTTCTACT	10391
rs749807368	snp	C/T	9.91015e-05	0.00703853	synonymous-codon	CORO2B	GRCh38.p7	15:68695145	TCCTCTGCAGACAGG[C/T]AGGATTGAACCCAAC	10391
rs749814273	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595813	CGGGCAAACAAATAC[A/G]GATGAAGCCATTGGC	10391
rs749821419	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68582649	GGTACATTAATAGAG[C/T]CGTGTGTAAAGTACA	10391
rs749838525	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68651797	TGCCCCGAGGCCACA[A/C]CTCCTGAGGGAGGCT	10391
rs749851541	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68663668	AGGAGCAATATTTGC[A/G]TTGCATATATCTGAC	10391
rs749886601	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68692673	GAGTCTCACTCTGTC[A/G]CCCAGACTGGAGTGC	10391
rs749930152	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68684820	GCCTCCTTCAGGCCC[A/G]GGAGCCTGGGACACA	10391
rs749976405	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654668	TAGTGCATGTTTCTC[A/G]GGGTGCTGTGATGAT	10391
rs749984624	snp	C/T	3.32425e-05	0.00407678	intron-variant	CORO2B	GRCh38.p7	15:68714709	GCCTGTGGGAGAGCC[C/T]TACCCTCAATGCACC	10391
rs750001854	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68572349	TTCACGTTACCTGCC[A/G]CTTGCCTTGCTTTTG	10391
rs750006596	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68716470	GTGTACCAGACCCTG[C/T]GCGAAGTCCAGTGGC	10391
rs750021023	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68632798	GGTTTTGCCACGTTG[A/G]TCAGGCTGGTCTCAA	10391
rs750031751	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68593011	TCCAAGAGCATTGCA[C/G]CAGCATCTGGTGAGG	10391
rs750034673	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68562225	GGTTGACTATGGGGT[A/G]CAGGTGGGAAAGCCT	10391
rs750069406	snp	A/G			utr-variant-5-prime, intron-variant	CORO2B	GRCh38.p7	15:68616601	AGGCCGCGGTCGAAT[A/G]ATTCTGACAAGCGGT	10391
rs750126927	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68674079	GGGGTTGACTGGGAG[A/C]GGGAGAGAGGCTGCG	10391
rs750143151	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68622585	ACAGCAAATCCTATC[A/G]TTGGACCTCACCGAC	10391
rs750165750	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68662568	CTTTGTATTGCCATA[C/T]GCAATTTATTGGAGA	10391
rs750191397	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68703433	TGGGATTACAGGTGT[G/T]AGCCACCTCGCCCAG	10391
rs750193586	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68633800	TCCTTCTCTTCCATG[C/G]CATCCCCTGGCTGTA	10391
rs750211307	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68582318	TTATAGGATGAGAAA[G/T]AGAAGAAAGCCAGAA	10391
rs750211362	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68692720	CTCCCTGCAACCCTC[A/G]CCTCCTAGGTTCAAG	10391
rs750228464	snp	A/G	1.66349e-05	0.00288395	intron-variant	CORO2B	GRCh38.p7	15:68695096	GGCCACCCCAGGGCC[A/G]TCAAACTAATCTCCT	10391
rs750237704	in-del	-/AGAG			intron-variant	CORO2B	GRCh38.p7	15:68669062	CTCCATCAGAAAGAA[-/AGAG]AGAAAGAGAGAGAGA	10391
rs750240470	in-del	-/GAA			intron-variant	CORO2B	GRCh38.p7	15:68632551	CTGCTTTAACAGTCC[-/GAA]CTCTCCCTGGATAAT	10391
rs750253612	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68675293	TCATGAGGATTTCAC[A/G]GTAACTTTGAGGACA	10391
rs750258597	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68704233	TGAGAGAGCAAGACC[A/G]TGTCTGAAAAAAAAA	10391
rs750281312	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68685096	CTGCTGGGTTCAGCA[C/T]GATCCACTGCCCTCG	10391
rs750285727	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68717516	GCTAAGGTATCGGAT[A/G]TGGAGGGGTGGAGAG	10391
rs750294947	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68685083	GTAAATCACCCATCT[C/G]CTGGGTTCAGCATGA	10391
rs750296865	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68721932	TGTTTTTAAACATTT[C/T]TGTAGAGACAGGGTC	10391
rs750303477	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68594215	GCATGGAAGGCTCTG[C/T]ACCCTCTTCCCCATA	10391
rs750306640	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68652185	AGATCTCGAAGGAGT[A/G]GCTCTGTCTTCCCCA	10391
rs750363748	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68583210	TGCCCAGGTAATAGC[A/G]GGCCTGCATTTTCCA	10391
rs750367796	in-del	-/GTT	1.68055e-05	0.0028987	intron-variant	CORO2B	GRCh38.p7	15:68719566	AGGTAAGGAATGTAA[-/GTT]ATTACCTCCACAGGC	10391
rs750376397	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68610271	GACAGGTTCTCTAGC[A/G]CCTCGCCTCGTTTAC	10391
rs750388056	snp	C/T	0.00011618	0.00762078	intron-variant	CORO2B	GRCh38.p7	15:68719407	CGTTTCCCTTGCCTT[C/T]TTTAGATCCCGTGCT	10391
rs750389874	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68623480	TGTTTACACCACCTC[C/T]TCACCCCCACCCCAC	10391
rs750399003	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68609407	CTGTATTTAAGAAGA[-/G]GGCTGTGGCTGTGCA	10391
rs750406670	snp	A/G	1.65051e-05	0.00287267	synonymous-codon	CORO2B	GRCh38.p7	15:68711658	CACCACCACGTGCAA[A/G]GACAAGAAGCTGCGT	10391
rs750429162	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68698122	GCACTGCCACCCCCA[A/G]ACTGAGGGTTGGTAG	10391
rs750429667	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68663436	GAATTTAAATGGATA[C/G]TTGAAGAGGTACGTG	10391
rs750432955	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630250	CTGTGTGGGGTGGTC[A/G]TGTGCAACGGGCAGC	10391
rs750442841	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68650884	TGTGCACTGGGTAAA[G/T]ACGAGGGGCCCCATC	10391
rs750469001	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68671558	TTCTGGTTCAGGGTC[G/T]CATTTGGTTGCGTTA	10391
rs750542270	snp	C/T	3.30344e-05	0.004064	synonymous-codon	CORO2B	GRCh38.p7	15:68713987	GAACATGAAGCGGCT[C/T]CTCACGACAGGGGTC	10391
rs750549774	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68602564	TCCCTATCGTGTACT[A/G]TGTTAAACAGGATCC	10391
rs750557711	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68696101	TAAAAAAAAAAAAAA[-/C]TAGGTGGGTGTGGTG	10391
rs750559705	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68590485	CACACAGCAGGAAGG[A/G]GCAAACTGGGCCATA	10391
rs750566966	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68683631	GGGAGCCTCACCTTC[C/T]CTCTGCAGTATCCCT	10391
rs750624202	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601499	GTGGGGATTGCGGCC[A/G]TGAGCGTGCAGTGCG	10391
rs750673447	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68606888	ACAGGGCAGGCACTT[C/T]GTAGGTGCTCAATAT	10391
rs750675718	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591445	CAGGGGCCATGGGGA[A/G]CTTTGGATGCCAAGC	10391
rs750687842	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68619681	TGTGTGTGTGTGTGT[A/G]TATATATATGTACAC	10391
rs750716992	snp	A/T	3.8841e-05	0.0044067	intron-variant	CORO2B	GRCh38.p7	15:68718652	GGTGATGTCACTGAG[A/T]CGCAGTTTCTGGGAC	10391
rs750729843	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68707809	CTGAGTTATGTACTC[A/G]CCAGCTTGTTCCCCC	10391
rs750732199	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566471	TCTGAGCCTGTGGGT[A/G]CCAAATGAGAGGTGC	10391
rs750736357	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68576470	AGAGCCCACAACAAC[A/G]GCGGATGGCGGGAAA	10391
rs750744161	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68679175	GGTGGAAGTGACATC[C/G]AAGGGAATCATCCCA	10391
rs750806603	snp	C/G	1.66095e-05	0.00288175	intron-variant	CORO2B	GRCh38.p7	15:68695289	CCCGGAGGAGGGTGG[C/G]CTCAGGCCCCTCCCT	10391
rs750807067	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678331	GTGAGCCCTTTCTCC[C/T]CTCCCTCACACTGAG	10391
rs750813085	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68563135	CCACACATTAAGGAA[-/C]TAGAAAAAGAAGAGC	10391
rs750820786	snp	C/T	1.65875e-05	0.00287984	missense	CORO2B	GRCh38.p7	15:68718745	GCCTGCGAGGTGTTC[C/T]GCTTCTACAAGCTGG	10391
rs750821107	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68662649	GCAGATACTTGCAAC[A/G]CTTGAGCTTCCTGCA	10391
rs750836365	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68586059	GCTAGGAATGCTGGC[C/T]TTGAAGTCAAACACA	10391
rs750867614	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68607663	TCTCTACAAAAAATT[A/T]AAAAATCAGCCAGGT	10391
rs750868528	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68565756	CCTGCCTCATGCTCA[C/T]GCCTCTCATTCCTTT	10391
rs750916630	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68709605	GGGACTATAAGCGTG[C/T]GCCACTACACCCGGC	10391
rs750919053	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68626708	CTCAGGCCCCATCAT[C/G]AAGTCCATTTCGTTG	10391
rs750926390	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68598685	TGGAGTTTTAATTCT[A/G]CCGCAAACCTAGCTC	10391
rs750934900	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68625588	TCCGTTACAGGTTTT[A/T]TTCTTGTTTGTTGTT	10391
rs750937464	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68666894	CAGGGTGGTATGGCC[A/G]TAGACCAGCCAAATC	10391
rs751017249	snp	A/T	3.29766e-05	0.00406045	missense	CORO2B	GRCh38.p7	15:68715252	ACGAGATCAGCACTG[A/T]GAAGCCCTACCTGAG	10391
rs751024165	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68687552	GAGGGCCCGGCCATG[A/G]CTGCCTGAGTGCATG	10391
rs751060072	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68677864	GTCCCCTCTACTGTG[C/T]CAAGAACAGGTCCTG	10391
rs751071333	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68675540	CCACTTAGTTGCTGC[A/G]TGATCTTGAGCAAGA	10391
rs751100563	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68562564	TACAAAGGAACCCCA[A/G]GTATTGCAGTGGGAA	10391
rs751104729	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68595485	CAGGGCTCAGATATC[C/T]GCTGTCCTCCTTTAG	10391
rs751109834	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703837	TATGCTGCATTCCAT[A/G]AAATGGAAACAAACT	10391
rs751111872	snp	G/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726970	TGTGCCCCTAGATCC[G/T]TCAGGTCCCCACCCT	10391
rs751137909	snp	C/T	1.65425e-05	0.00287593	intron-variant	CORO2B	GRCh38.p7	15:68695127	TCTCTCTCTCTCTCT[C/T]TCTCCTCTGCAGACA	10391
rs751151273	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574741	CATAAAGAGACAGAA[A/G]CAAATATATTTCATT	10391
rs751171026	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68718215	AACAGCAATCTTAGG[C/T]TGCGTCCAGACCTCT	10391
rs751183138	in-del	-/A			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577474	CATGTCTGTAATCCC[-/A]GCACTTTGGGAGGCC	10391
rs751201680	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68704845	AGTAGTTTTGCCACT[A/T]CTCCCCACCCTTTCC	10391
rs751207002	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68676482	AGGATAACCACCGCT[A/G]CCTAAACCCGTCAAA	10391
rs751264417	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68633929	GTGACAGGGAGCAAC[A/G]TCTTGGTCTGTGGGC	10391
rs751295241	snp	C/T	1.65567e-05	0.00287716	missense	CORO2B	GRCh38.p7	15:68695252	CGTGCTCGGAGGACA[C/T]GTCGGTGAGCAGAGG	10391
rs751301808	snp	A/G	3.3117e-05	0.00406908	missense	CORO2B	GRCh38.p7	15:68719418	CCTTCTTTAGATCCC[A/G]TGCTGATGTCTTTGA	10391
rs751351546	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570795	CCCAGGCCCACTACA[C/T]GTAGTTTTTTTTTTT	10391
rs751351866	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68611575	GAAAGCATGTCATAG[C/T]TAATTACTACATCTT	10391
rs751370714	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68569244	TCCACCATCACAGTA[A/T]CACACAGAGTAGTTT	10391
rs751384447	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68724455	TTTTGAGACATTGAG[G/T]TATAATTTGCCTATG	10391
rs751387768	snp	C/T	1.65241e-05	0.00287433	synonymous-codon	CORO2B	GRCh38.p7	15:68711688	TGTGATTGAGCCCCG[C/T]TCTGGCCGTGTTCTG	10391
rs751432542	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68601800	GAGGGCTATTGTCTT[A/C]GTCCCTCTGTGCTGC	10391
rs751439958	in-del	-/GGGATAAAAT			intron-variant	CORO2B	GRCh38.p7	15:68720833	CATGCTTGAGGAGAG[-/GGGATAAAAT]GGGAGCCATCTTAAA	10391
rs751467922	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68558525	GACCACAGGCATGCG[C/T]CACCATTCCCCCAGG	10391
rs751502670	in-del	-/AGAG			intron-variant	CORO2B	GRCh38.p7	15:68669070	GAAAGAAAGAGAGAA[-/AGAG]AGAGAGAGAGAGAGA	10391
rs751528864	in-del	-/CC			intron-variant	CORO2B	GRCh38.p7	15:68637746	AGTTCTCCTGGGCTC[-/CC]CCCACATTACACAGC	10391
rs751539421	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68612446	ATGTCCAACACTGCA[A/G]AGGAGTCCTGGAATA	10391
rs751548499	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68717101	CTGAGGTCAGGAGTT[C/T]GAGACCAGTCTGGCC	10391
rs751549062	snp	G/T	1.65272e-05	0.0028746	synonymous-codon	CORO2B	GRCh38.p7	15:68713999	GCTCCTCACGACAGG[G/T]GTCTCCAGGTGGAAC	10391
rs751555481	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68653374	ACGGTGGGAAACTTG[C/T]CTGGTTTGCACAGGG	10391
rs751572529	snp	A/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639880	GAGTGTGTTCTGCTC[A/T]CACTAGAATCAGTCA	10391
rs751587483	snp	C/T	0.00126024	0.0250705	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68579243	GCGCCCGCGCCCCCG[C/T]TCCGCCGCGGAGTTT	10391
rs751591119	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68674141	CCTCCCACAGAGTCT[-/AA]GAGCTTGGATGTGGC	10391
rs751606183	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703276	CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGATTAC	10391
rs751610818	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68580654	GGCCCACCTGGGGTA[A/G]GATGCTTAGGGTTTT	10391
rs751612040	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68673414	GTCCGGCTACTTGGG[A/T]GGCTGAGGTAGGAGA	10391
rs751622576	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68660825	ATTTATTGCCTCAGG[A/C]TTGATGGCTTTCACA	10391
rs751686978	in-del	-/AT			intron-variant	CORO2B	GRCh38.p7	15:68610520	CACATCCCCTCCCTC[-/AT]ACATCCTCTCTCCCC	10391
rs751696221	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68603213	AGGGCTAACACAGTA[C/T]GTGGTCGCAGTAGGT	10391
rs751742669	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68607957	GTCAAAATCACATGC[C/T]CTTGGGCATAGCACC	10391
rs751786257	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68576832	TTGTTCTTGGTGGCA[A/T]TAAATATTTGCTAAG	10391
rs751799847	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68609804	CCTGGGACTGGAGGG[A/C]TGTACAGCAGCCTGT	10391
rs751818415	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68638301	ACTCCCTCACAGGAG[A/G]AGGAGAGAGGGTAGA	10391
rs751820379	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68711932	CTGTCCCCACTGCAC[A/C]CCCTACCTCCAGACA	10391
rs751884740	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68626754	AGGTGTCAGTACTTA[C/T]GAAAAAACGTCTCCA	10391
rs751892632	snp	C/T	1.64776e-05	0.00287028	synonymous-codon	CORO2B	GRCh38.p7	15:68710863	CAACATCCTGTTCAG[C/T]GCTGGCTACGACTAC	10391
rs751925800	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68616649	CGCGTGGGCCCCAGC[A/G]CAAGCAGGCAATCCC	10391
rs751948509	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68680877	TCAGTAAATGACAGC[C/T]AGCATGATCACAAAT	10391
rs751953715	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68573893	CAGCTAGACCATTCC[A/T]ATCACAGTCTAGGAA	10391
rs752016153	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726376	ACATCTCAGCACTCC[C/T]GCCTGGAGCTCTCAG	10391
rs752016954	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68599847	GTGCTCGAGGCCTGA[A/G]TGAATTCAGGGACTA	10391
rs752040570	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618547	TGCGCAGCTGAGGAG[A/G]TAGCACTGATGTGCC	10391
rs752072407	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68655829	GACTTGCTGTTGTGT[C/T]TCATCTGAGCCTGTA	10391
rs752077635	snp	C/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615971	GCAGGGTGGAGGAGG[C/T]TGCCGTTTATAGAAC	10391
rs752079257	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68656804	GCCTCAGTTTCCTTC[A/G]CTGTAGAATGAGAGA	10391
rs752105263	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68704019	GGCAATATGGCAAAA[-/A]CCCTTTCTCTACACA	10391
rs752108603	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68675174	AGGCAGCCATGATGG[C/T]GAAAATACTTCTAGT	10391
rs752158574	snp	A/G	4.66494e-05	0.00482934	missense	CORO2B	GRCh38.p7	15:68710736	TCCCTCTGCAGGTGC[A/G]GATCTGGGAGATCCC	10391
rs752191603	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658415	CTTCGGCCAGTGAGG[A/G]GCCAGTGGGGGTTGT	10391
rs752215859	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68634758	CTGCAAGTTTGAGAA[A/G]CACTGAGCTGGAGAG	10391
rs752251203	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595732	CTCTGTACTGGCTCA[A/G]TGGACACACAGAGGG	10391
rs752254851	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68564192	TGGCACTTTTTATTA[C/G]TTTAATAAATATTGT	10391
rs752263378	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68718353	CCCCTGCTGTGCTCT[A/G]TGACCTTGGGTAACC	10391
rs752298448	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68707439	ATTACGAGCATGTTT[C/G]TCATAGAATAAATTG	10391
rs752360427	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68586875	GAGGCCCTCCTGGCT[C/G]TCAGGCAGGAGGGAG	10391
rs752375213	in-del	-/A			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578609	ACTTTGCGAGCCTCC[-/A]GGGGGCGAACCCGAC	10391
rs752375793	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597014	AAGTCCTCAGGGACC[A/G]CCCTCCCCTGCCAGC	10391
rs752396621	in-del	-/TAAAAAAAAAAAAAAAAAAAAA			intron-variant	CORO2B	GRCh38.p7	15:68650356	GAGCGAAACTCTGTC[-/TAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	10391
rs752421094	snp	C/G	1.65553e-05	0.00287705	missense	CORO2B	GRCh38.p7	15:68714023	GTGGAACACAAGACA[C/G]ATTGCCCTCTGGGAC	10391
rs752428698	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68583838	TTGGTGAAGAGGAAG[C/T]GGGGGTACCAGCACA	10391
rs752445408	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640943	CCAGGACTGCAGACT[C/T]CCAGCTCAGGGTTCT	10391
rs752465632	snp	C/G	1.6633e-05	0.00288378	intron-variant	CORO2B	GRCh38.p7	15:68725826	CCTCCTTGGCCCCCT[C/G]TCTTCCTCCACCCCA	10391
rs752498441	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68695809	TTCAATGAGAAGAGA[C/G]AAGAAACAGGAGAAG	10391
rs752509020	snp	G/T	2.17455e-05	0.00329731	intron-variant	CORO2B	GRCh38.p7	15:68645110	GCCCAGCCGAGGCCC[G/T]TCATGGCACAGGGCC	10391
rs752512624	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68713811	CAAATAAGGAAATAA[C/T]TGCAGGGGCCAGGGC	10391
rs752518423	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68571911	AGTGCAGGGAATGAA[A/G]TGATGTAACCGGGGT	10391
rs752604882	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631734	ATGCTGCAGGTGTTC[A/G]GGGGAGGGTAGGTCC	10391
rs752610781	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591619	CAAAGCCTATGTGCA[A/G]TGAGGCGGGGAAGGG	10391
rs752634751	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68628282	CCTATGGAGTGGAAG[G/T]CCTGGGTTTGAATCC	10391
rs752641558	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68641639	GCCTATCAGGTCAGC[A/G]TGTCCTGTGCTGGGC	10391
rs752677761	in-del	-/AAA/AAAAAA/AAAAAAAAAA			intron-variant	CORO2B	GRCh38.p7	15:68576152	GTGAGACTACGTCGC[-/AAA/AAAAAA/AAAAAAAAAA]AAAAAAAAAAAAAAA	10391
rs752693972	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68568019	GTGAGAGTCCATCTC[A/G]AAAAGAAAAGAAAAG	10391
rs752719679	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68671858	GACCAACCCTGGTGC[A/G]ATATGGGAGGGGACT	10391
rs752726436	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68692457	GGGCATGATGGCTGA[C/T]ACGTGTAGTCCCAGC	10391
rs752765898	in-del	-/CA			intron-variant	CORO2B	GRCh38.p7	15:68627016	TTCAGCTCCCAGTCC[-/CA]CCACTGCCAAGTGGG	10391
rs752781948	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68582093	CTGTTTTCCATTTTC[C/T]GCCTCTCTTTCATAC	10391
rs752828037	in-del	-/C	0.000216321	0.0103978	intron-variant	CORO2B	GRCh38.p7	15:68725819	CTGGGCCCTCCTTGG[-/C]CCCCCTCTCTTCCTC	10391
rs752838172	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68566857	AGCTACCAAACACAG[C/T]GTCATGTGCAACACA	10391
rs752876671	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68557379	TCATAGCAGAGCTGA[C/G]GTTCAGTGGCCAATG	10391
rs752882024	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68599912	CAACGAGGATGCATC[A/T]TAATGAACTGCGTCC	10391
rs752892880	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600898	AATTTCCCCACAACC[A/G]CAACACCACCTTCCC	10391
rs752903869	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68587976	TGCTCCTTACTGTGT[C/G]ACCTTGGGCTAGTCC	10391
rs752916730	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68646608	CACTTGATGGCGGGA[A/G]GTCTGGGTTCTGCCC	10391
rs752938703	snp	A/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639716	GCTGACTACCTATCA[A/T]GGTAGCTTCTTTTTC	10391
rs752956479	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68668021	GTTGAACACGTACAA[A/C]GGGCCAGGGACTGTT	10391
rs752982762	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68611245	TTTTAAAAAATAACA[A/G]TGTCTATTTCAGATT	10391
rs752991019	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68656894	GGAAGGTGCCTGGCT[C/G]AGGGCAAACCTTTCA	10391
rs752998546	snp	C/T	1.6646e-05	0.00288491	intron-variant	CORO2B	GRCh38.p7	15:68711535	TCCCATGCATCTGCC[C/T]TCGCAGGTCCTCATC	10391
rs753002741	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68700121	AAGCACCTGAGGCAT[C/T]GGCCACCGAGGCCCT	10391
rs753028697	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68638382	TTGTGTTTGGTCACT[C/T]CATTGTATCCAGTGA	10391
rs753049667	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678059	CAGGAGCTCTCCTTT[C/T]CCCTGCAAGGTCTGT	10391
rs753081202	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668992	CTGAAGCAGCAGAAT[C/T]GCTTGAACCTGGGAG	10391
rs753083692	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68574899	GGCCCCAGAGGCCCA[G/T]GAAAGAGCATGGCCT	10391
rs753098418	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68563204	AGATTAGAGTAGAGA[A/C]TGGCCAGGCACCATG	10391
rs753100035	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68673450	TTGAGACTGGACAGT[C/T]GAGGCTGCAGTAAAC	10391
rs753127045	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68634011	CGGTCAGGGCATGTC[A/G]CAGGCAGGGAGCCTC	10391
rs753136125	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68717713	ACTCAGACCGAATCT[C/G]CTGGCTCTTAATCCC	10391
rs753153879	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68617863	CCTTAGAGATTGTGG[C/T]TGAATGTGGGGGTTT	10391
rs753166005	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68652639	TGGGATGGTGCATTC[G/T]CCTTCCCCACCACAG	10391
rs753193847	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68605917	TTTAGTAGAGACGGG[A/G]GTTTCACCATGTTGG	10391
rs753198678	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68644356	TCTAGATTGGGACCC[A/G]GTAATCAGCATTTCT	10391
rs753228038	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68645836	TGAAGTTCAATGGCG[C/T]GATCTCGGCTCACTG	10391
rs753244869	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600409	GACTTCCCTGAGTAC[A/G]CACTATGCTCCCTTC	10391
rs753271382	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68658060	TAGGAAACCTAGCTT[C/T]TCTGCCTGGTTCTTT	10391
rs753286460	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68708674	GCCCTGCCTTTGGCT[C/T]TCTTCCTTTTTTTTT	10391
rs753306754	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68687612	ATTAACTATATAATT[G/T]TATTTAATTTCAAAG	10391
rs753334240	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68653655	AGAAGTTGGTGGATC[A/G]TTTAGCTCCATAGCT	10391
rs753340984	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68666688	ACTGGGGGTTGGGGT[G/T]TTGTGTTGGGGGATG	10391
rs753346470	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625296	TAACTCGGGTTCTTC[A/G]AGGTATAATTTACAT	10391
rs753400617	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68585108	AGCAATGGGAGGCTC[A/C]CAGGTTTGCTCAGGC	10391
rs753408024	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68611923	ACTAGAGGTGTGCAC[C/T]ACCATGCTGGCTAAT	10391
rs753413234	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68641763	AGAGTTCGGCACTGT[C/T]GCCCAGGTGGTAGTG	10391
rs753430903	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68678898	TACTGGACAGATAGT[G/T]GATCTGGCTAGAGGC	10391
rs753432679	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68664785	GAGGTTGAAAATATC[A/G]TCGTATGCTTACAAT	10391
rs753435375	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68572074	CCCAGGGGCATCTGG[G/T]AAGGGGCTGTGGGCT	10391
rs753478947	snp	A/G	1.65825e-05	0.00287941	intron-variant	CORO2B	GRCh38.p7	15:68714517	GGGGAGGGGTATGCC[A/G]TCCTGCCTGCAGAGA	10391
rs753493170	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727275	CCCTTCTGCAGATGA[A/G]GAAACCGAGAGAAGT	10391
rs753494290	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68589493	TGGACTGCTACAGCC[A/G]GAAGGGACTTTAAAG	10391
rs753505180	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68654556	TTCTAGGGCCTGGAG[C/G]CTCCCATACCTTTGG	10391
rs753539393	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68683775	TGGCCTTGGTCAAGA[C/T]CACTGTCATCATGGT	10391
rs753539596	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68697505	CACAGTACCTAGTAC[A/G]TGGGAGAGTGGTGAG	10391
rs753557414	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68614138	TCTCTGGGAGTGGTC[C/G]CTAGAATATATGTCT	10391
rs753567077	snp	A/G	1.65693e-05	0.00287826	missense	CORO2B	GRCh38.p7	15:68645200	GCTCCAAGTTCCGGA[A/G]TGTCTACGGGAAGGT	10391
rs753568771	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68653030	TCTCTTTTGGAAGCC[A/G]AGAGAGTAGATGTTT	10391
rs753576773	in-del	-/GAAGAG	1.65015e-05	0.00287237	cds-indel	CORO2B	GRCh38.p7	15:68719489	TCCCATCAAAGAAAA[-/GAAGAG]TGTTGTGGTCAACGG	10391
rs753582131	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68591689	CCTGTGCCTGGGAGC[C/T]GGGTGTCACATATGC	10391
rs753658629	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68716305	CCCTCTAAGTCTCAG[C/T]TTCCTCATCTGTAAA	10391
rs753658680	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68703534	AAGTAGCTACTAAGG[G/T]GTTAGATATCAGATC	10391
rs753659825	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68654620	TAGGCATCTAACATC[C/T]GTTTCTCAGTTTCCC	10391
rs753665612	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68684713	TGGTGTGACCAGGGG[A/C]AAGTGTCCTTATTTA	10391
rs753693651	snp	A/G	0.000115438	0.00759643	missense	CORO2B	GRCh38.p7	15:68645296	GTGCCGTCAACACCC[A/G]CTTCCTGGCCATCGT	10391
rs753702940	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68703078	GTGATCCACCCGCCT[C/G]GCATCCCAAAGTGCT	10391
rs753726697	snp	A/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726274	TTGGCAGGGGCTCCA[A/T]CTCAGTGGACCAGGA	10391
rs753755951	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68629950	GAATCCAAAAGGATA[A/G]GTAATGCCCCTGCCA	10391
rs753792088	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68597616	TCCCTAATTTCTGTT[-/C]TCCCCCCCATCAAAA	10391
rs753793619	snp	C/G	4.96726e-05	0.00498335	intron-variant	CORO2B	GRCh38.p7	15:68719258	GCGGGGGGCTCCACA[C/G]AGCACAGGCGGCTGC	10391
rs753846751	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68558349	TGGGGTTGGAGAGGA[A/G]AGCAAAAACTCCCTT	10391
rs753850944	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68669120	AGGAAGGAGGGAAGG[A/C]AGGAAAGAGAAAGAA	10391
rs753945071	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574964	CAGAACTAATACTGC[A/G]ACGTCTTATTTACCC	10391
rs753972709	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601108	TTTGTGGGTGTGTGA[A/G]TGGTTGACAGGTAGA	10391
rs754070613	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68625505	TTCCATCTGTAGAAG[C/T]TGTTTTTTTCCAGAA	10391
rs754093870	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68601693	GAATGGCTGTGTGTG[C/T]GAAGGCCGGAGAAGA	10391
rs754097542	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618040	CAGTACCTGCCCTCC[A/G]GGAACCCAGTTAGTG	10391
rs754117853	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68629394	GTTGGAGGAAGAGGC[A/G]CCTTTCTCTATTCTC	10391
rs754127891	snp	A/C			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577876	GCACTTTCCACAGAG[A/C]AGGTGCTCATATATG	10391
rs754132983	in-del	-/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616372	GAAAAGTATTTAGCA[-/T]TATTTTTAGTCTTAT	10391
rs754133751	snp	A/G	0.000123119	0.00784502	intron-variant	CORO2B	GRCh38.p7	15:68718687	TGGAGCCACATGTGT[A/G]CCTGTTACAGGGGTC	10391
rs754148048	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68688737	CCCATTGCTGTCCCT[A/G]TGATAAATAACATGG	10391
rs754164634	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68700985	TAGATGATGCCCCTC[C/T]CTGAGGAGCTGGGGG	10391
rs754182653	snp	C/T	1.64904e-05	0.00287139	missense	CORO2B	GRCh38.p7	15:68715276	ACCTGAGTTACCTCA[C/T]GGAGTTCCGCTCCCC	10391
rs754224556	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658234	CCAGAAGCTTGGGTC[A/G]GTAGGAGCCCTGGAC	10391
rs754232541	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564407	CTCTTGGGCTCAAGC[A/G]ATCCTCCCCCATCAG	10391
rs754276860	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68624574	TTAGTTGTGCATTCA[A/G]ATCACCTTGGGGGCT	10391
rs754292687	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68576486	GCGGATGGCGGGAAA[G/T]GTGCCAAGAGGCATG	10391
rs754326115	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606537	AGTTGTTGGTCAGGC[A/G]CTTTCCTTAAAGTAA	10391
rs754327006	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68680813	TAAGGTTATTGTGCT[-/A]AAAAAATTGAAATAA	10391
rs754387523	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68594627	GAATATGAGAAAGGG[C/G]CTCTGTTTATTGAAC	10391
rs754392179	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68576058	CTCAGGAGGTGGAGG[G/T]GGGAGAATCGCTTGA	10391
rs754393269	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68704605	AGCTTTATTAACTGT[C/T]CTTATCAGCTGCCTT	10391
rs754406372	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68707162	GCTAGGATTACAGAC[A/G]TGAGCTACCACGCCT	10391
rs754448616	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68644245	AGCAATCCAGATTGC[A/T]TTAATCATGTGCTTT	10391
rs754459914	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68662791	CTGCAAATGACACCA[G/T]GTATGATCTGAAAGT	10391
rs754496220	snp	A/C	1.65359e-05	0.00287536	intron-variant	CORO2B	GRCh38.p7	15:68695131	TCTCTCTCTCTTTCT[A/C]CTCTGCAGACAGGCA	10391
rs754512751	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604841	AGTTTTGAGGCTGGG[C/T]ATGGTGGCTCACGCC	10391
rs754512983	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68644666	GGGATGACAGTGGAT[-/G]GGGGGGTTGCCTTCT	10391
rs754568818	in-del	-/GCTGGGTTCA			intron-variant	CORO2B	GRCh38.p7	15:68685104	TCAGCATGATCCACT[-/GCTGGGTTCA]GCCCTCGGTACTCCT	10391
rs754571396	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68706447	AAGTTCAACACCACA[C/T]CCCACTGGCTCATAG	10391
rs754598248	in-del	-/TG			intron-variant	CORO2B	GRCh38.p7	15:68653874	GGAAAAAAAAAAAAA[-/TG]CCTGAATCTTCATCA	10391
rs754615170	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68663493	ACACGCGCACACACA[C/T]GCAGAAGAATTTCCT	10391
rs754641684	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68693981	GCTGGGATTACAGGC[A/G]TGTGTCACCATGCCT	10391
rs754650422	snp	A/G	8.2633e-05	0.00642726	missense	CORO2B	GRCh38.p7	15:68719426	AGATCCCGTGCTGAT[A/G]TCTTTGAAAGAAGGC	10391
rs754673525	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68612485	GGTGATGTGGAAGTG[A/C]GTGCTCTGAGGTCTG	10391
rs754685843	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68723426	GGCGCCCAGCCAATA[A/G]ATACATTTGGTTTCT	10391
rs754731134	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68623713	GGAGCAGCAGCAGCG[G/T]GTGGGAGGGCAGGCA	10391
rs754744141	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68601348	GTTGAGGGTTCCACC[C/T]GTCCCTGGGCCTCAT	10391
rs754767346	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68694914	TGTCCCACCATGGCT[C/G]TGTGGCCTCCCTGAA	10391
rs754781568	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68586337	CAGGGAACTCTGGGA[A/C]TAGCAGGGGGCCTGA	10391
rs754798298	in-del	-/AAAAAAAAAAA			intron-variant	CORO2B	GRCh38.p7	15:68576164	CGCAAAAAAAAAAAA[-/AAAAAAAAAAA]AAAAAAAAAAAAGAA	10391
rs754801831	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68691546	GGAGAATGGCGTGAA[-/C]CCCGGGAGGCGGAGC	10391
rs754809675	snp	C/T	3.30693e-05	0.00406615	missense	CORO2B	GRCh38.p7	15:68711695	GAGCCCCGCTCTGGC[C/T]GTGTTCTGCAGGTGG	10391
rs754810141	snp	C/T	1.68448e-05	0.00290209	intron-variant	CORO2B	GRCh38.p7	15:68719570	AAGGAATGTAAGTTA[C/T]TACCTCCACAGGCCC	10391
rs754814558	in-del	-/AAAG			intron-variant	CORO2B	GRCh38.p7	15:68669157	GAAGAAAGAAAAAGA[-/AAAG]AAAGAAAGAAAAGAA	10391
rs754834022	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68611638	CTACAATTGATTGAA[A/T]TAGATTTATTAAGAT	10391
rs754855764	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68624415	TGATATTAGAATCAA[C/T]AGTGAGCACGACTAC	10391
rs754897969	snp	G/T	1.65266e-05	0.00287455	missense	CORO2B	GRCh38.p7	15:68714000	CTCCTCACGACAGGG[G/T]TCTCCAGGTGGAACA	10391
rs754900633	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68670471	AGGCATGAGCCATCG[C/T]GCCCAGCCAGCAAAA	10391
rs754938980	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68713481	AGGTGGCTGAAAACA[A/G]CAGAAATGTATTCTC	10391
rs754949243	snp	C/G	7.60427e-05	0.00616568	intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68579249	GCGCCCCCGCTCCGC[C/G]GCGGAGTTTCTGCAT	10391
rs754953705	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68724497	CCTCTGTAGTGTGTC[A/G]GTTTAAGAGTTTTGA	10391
rs754959381	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68649492	ACACAAAGGGACACT[A/G]TGCAGTCATTAAAAT	10391
rs754963068	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68559793	CAGGGGGCGCGGCCC[A/G]CATCCTTCCTCGGAG	10391
rs754983726	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682707	CTTTTCGGAGGGAGA[A/G]ACTGAGACCTAGAGA	10391
rs755043676	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68719991	GAAGGTGCTCTCTGT[A/G]CCACTTGGAATGGGA	10391
rs755044512	in-del	-/CTT	1.65899e-05	0.00288005	intron-variant	CORO2B	GRCh38.p7	15:68695110	CATCAAACTAATCTC[-/CTT]CTCTCTCTCTCTCTT	10391
rs755045530	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603214	GGGCTAACACAGTAC[A/G]TGGTCGCAGTAGGTG	10391
rs755046356	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606969	CTGATCAGAGCCTTC[A/G]CACCCAAAGCTGGAG	10391
rs755062931	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68604505	AATTAAAAAGGTGTG[G/T]TTTTTTTTTTAAAAG	10391
rs755065728	in-del	-/A	1.66418e-05	0.00288455	intron-variant	CORO2B	GRCh38.p7	15:68725818	CCTGGGCCCTCCTTG[-/A]GCCCCCTCTCTTCCT	10391
rs755089670	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68710527	AGAGAAAACCTCCCA[C/T]AGGCAGAGAGATGGT	10391
rs755089698	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68683170	CCAGGGTCCTCCATG[C/T]CTATATCTCTCTCTA	10391
rs755123718	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68680934	CTTAGGGAAAAGGGG[C/T]CGGGCGCGGTGGCTC	10391
rs755123801	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68667083	CGCTCCTGATCTCCC[G/T]TCACTCTCATGCTCC	10391
rs755154726	snp	C/T	5.05191e-05	0.00502563	synonymous-codon	CORO2B	GRCh38.p7	15:68718798	GCCCATCTCCATGAT[C/T]GTGCCCCGGAGGGTA	10391
rs755169184	snp	A/G	7.90561e-05	0.00628664	missense	CORO2B	GRCh38.p7	15:68710769	AGGGCGGGCTGAAGC[A/G]GAACATGACGGAGGC	10391
rs755209576	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68566626	CACCCCTCACTCTGC[C/T]CCATTCCTGCTCCAC	10391
rs755211640	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68679706	ACTTCTAGGGGTTCG[A/G]AGTGCAATATGTTCC	10391
rs755220802	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68586585	TCATGGCATAGGTTA[C/G]TGTTATCATCCCTGC	10391
rs755245370	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68710049	GCCACGTGGTCTCCT[C/T]TCTGCTTCTCTCTGC	10391
rs755325445	in-del	-/GA			intron-variant	CORO2B	GRCh38.p7	15:68700806	GCCAGCAGCCGCGGA[-/GA]GAGAGAGAGGTTTCT	10391
rs755347536	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68587853	GACTCAGCCTGCCTC[G/T]CAGGCCTTCTGTCTT	10391
rs755377034	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68619171	TTCCTTTTTACTTTG[A/G]CTGCTAGGAAGCCCA	10391
rs755383170	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68592368	TTCTGTCTATTTCAT[G/T]GGGAGAGCCCTCATC	10391
rs755387715	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68656807	TCAGTTTCCTTCGCT[A/G]TAGAATGAGAGACAT	10391
rs755389562	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68667948	TTCTTATTTGTAAAC[A/G]AGAGATAATAAATCC	10391
rs755421540	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68711257	ATATCCTCAAAAAAA[G/T]GTGGGCTGACCACAT	10391
rs755430895	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68574797	GCGACCATGGATACA[G/T]CGCCAGGAGAGCTAC	10391
rs755441295	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68698264	TGGCTCATGTCTTAC[C/T]CAGGGACCCAGCTAG	10391
rs755444338	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68716605	GCAGAGAGTCAAATG[C/G]TGTGCTAGAACAGAA	10391
rs755447325	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68677977	TCATGAAAATCTCCT[G/T]CCTCTCGGAGGCCTG	10391
rs755455825	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68675604	TCTGAAGTTAGGGAA[A/G]TGATAACTCCTCCAC	10391
rs755462544	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68643237	GTTGGTGTCCTGATG[A/G]GGAGCCAGTGCTTGG	10391
rs755466918	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595222	TACTCTCTTGAGCTG[A/G]ACCCTACCCTGCCTC	10391
rs755473699	snp	A/C			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727002	AGCTGTCACCACCAC[A/C]CTCCCCAGGGGACTC	10391
rs755488663	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68686328	GGAGTGAGCCACCAC[A/G]CCCGGCTTCATACAC	10391
rs755514470	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68573901	CCATTCCAATCACAG[G/T]CTAGGAAGGCTTTCT	10391
rs755518983	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68597080	AGAAGCATATATATC[-/T]TTTTTTTTTTTTCCT	10391
rs755530055	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726377	CATCTCAGCACTCCC[A/G]CCTGGAGCTCTCAGC	10391
rs755533371	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68583841	GTGAAGAGGAAGCGG[G/T]GGTACCAGCACAGAC	10391
rs755538302	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603936	AGAGTGCCATGTTGT[A/G]GAATTCAGAAGGGCA	10391
rs755543913	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68652484	AGGCCACAGGAAGAA[A/C]AGGGCTAGAAACAGA	10391
rs755546909	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68655040	TGGGTGCCTGGAGAT[A/G]GGGGATTCTAGGGAG	10391
rs755549979	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68686464	ATGATAGCTCCTCAC[C/T]TCCCAGACAAGTCAC	10391
rs755577167	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68699348	CTACACGCTCCAGGG[A/C]ACCAAGGGGACCTGT	10391
rs755586775	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68634795	CCAACTGAATCATCT[A/T]TGTGAACCACCTGGA	10391
rs755695207	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68623750	GGTGAGGATTACCGC[A/G]TGCTGGATCACGGCT	10391
rs755711834	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640089	TGCCTGCGCACCCAT[G/T]CATCTGACCTCACAG	10391
rs755727497	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68610021	TGATAAAACCTGGCC[A/G]GAAACTCAGGCATAG	10391
rs755736891	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682849	CCCAAATCCCAGGTG[A/G]GCTGGGCAAAAATCA	10391
rs755740870	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68653617	TGCATGGCCCAGCTG[C/G]TCTTAACTCTGGAGC	10391
rs755755867	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68656998	GATCCCCAGTTTGCT[-/C]ATTTATCTCATGAGA	10391
rs755763070	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68683999	TAGGGACCCATTGAA[-/G]GATTTTGGAGCTGGG	10391
rs755779966	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570593	GAGGAACCCCAAATA[C/T]GAAAGTTGAAGTGCT	10391
rs755782066	snp	A/G	1.70435e-05	0.00291915	intron-variant	CORO2B	GRCh38.p7	15:68719580	AGTTATTACCTCCAC[A/G]GGCCCTGGAAGAGCA	10391
rs755804205	snp	C/T	1.65729e-05	0.00287857	missense	CORO2B	GRCh38.p7	15:68714028	ACACAAGACAGATTG[C/T]CCTCTGGGACCAGGT	10391
rs755815517	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68558949	GATAGTGGGTGAAGA[A/G]GTGACCCACGCCGGC	10391
rs755821190	snp	A/G	3.31807e-05	0.00407299	intron-variant	CORO2B	GRCh38.p7	15:68714512	GATTTGGGGAGGGGT[A/G]TGCCATCCTGCCTGC	10391
rs755828959	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68717333	AAAAAAAAAGATTTC[-/T]CTGGCTTCAGTAGAG	10391
rs755861629	snp	A/C/G	4.22433e-05	0.00459567	intron-variant	CORO2B	GRCh38.p7	15:68645128	ATGGCACAGGGCCCA[A/C/G]CCTGACCCTTGTCTC	10391
rs755877184	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68612785	GGGGCAGGAAGATCT[G/T]TAGGATTCCACCAGC	10391
rs755882810	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68590770	TAGGTGCAGGAGGGG[C/T]TCCTGAGAGGCAAAT	10391
rs755904376	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641001	GGAGTGGAGCTCCAC[A/G]CCCAGGGTTGTGGAG	10391
rs755922516	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68714086	GGCTAAAGGAAGCAT[C/T]GTTGCCTCGGAGGTC	10391
rs755943804	in-del	-/AAA/AAAA/AAAAA			intron-variant	CORO2B	GRCh38.p7	15:68647689	TCGAAACTCCATCTC[-/AAA/AAAA/AAAAA]AAAAAAAAAAAAAGA	10391
rs755967886	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68652283	CCAGCTCTCTGGAGT[A/G]GAATGTTAAGCTGCA	10391
rs756000048	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68614085	TGCTTGTTAAAATGC[A/G]GATTCTTGGGTTCTC	10391
rs756001146	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68670707	ATCTGCTAAGCAAAT[A/G]AAGATATAAGCAACC	10391
rs756020831	snp	C/G	3.34286e-05	0.00408818	missense	CORO2B	GRCh38.p7	15:68645185	GTCCGCAATACCGTA[C/G]CTCCAAGTTCCGGAA	10391
rs756068419	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68703322	CGCCCAGTTAATTTT[G/T]GTATTTTTAGTAAAG	10391
rs756075547	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68659762	AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT	10391
rs756140086	snp	G/T	1.70866e-05	0.00292284	synonymous-codon	CORO2B	GRCh38.p7	15:68718807	CATGATCGTGCCCCG[G/T]AGGGTAAGTGGGGCT	10391
rs756169999	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68712505	TTGGGGATGTGGGAA[G/T]CTCAACTAGTAGGTA	10391
rs756257604	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68558937	GAAATAAAATGCGAT[A/G]GTGGGTGAAGAGGTG	10391
rs756260631	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68638438	CAGTTAAGGAAACTG[A/G]TATTCAGACAGGTTG	10391
rs756283547	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68681107	AATCCCAGCTACTCG[C/T]GAACCTGAGGCAGGA	10391
rs756286567	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68656017	GCTCCTACCACTGGC[C/G]TTTCTCCTGGCAGCT	10391
rs756288580	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68669034	GGTGAGCCAAGACCA[A/C]ACCACTGCACTCCTC	10391
rs756296245	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68711389	GATGTATCAGCCTTT[C/T]CATATAGAACTCAAT	10391
rs756299590	snp	A/C/G/T	9.90422e-05	0.00703656	intron-variant	CORO2B	GRCh38.p7	15:68719111	TTCCCAGCAGCCCCC[A/C/G/T]ATGTGTCCTCTCTTC	10391
rs756327250	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68628184	CTCCAGTGCCTTCTA[C/T]GTGCCAAGCACTTTG	10391
rs756344565	in-del	-/C	1.67142e-05	0.00289081	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68725976	CAAGAACTGTTAGCT[-/C]CCCCAGCTGGGCTGT	10391
rs756353852	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68600932	TGTCCTGCTGATTCT[C/T]GGTTTCTAGAAATGA	10391
rs756385227	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574107	GATCTGTGTGTGCAA[A/G]AGCTGCTGGGGGAGA	10391
rs756389544	snp	A/G	4.60119e-05	0.00479623	intron-variant	CORO2B	GRCh38.p7	15:68710895	AGGTATGCAGTGGGC[A/G]GGCAGCTGGGTGGAG	10391
rs756402791	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68597641	CAAAAAAAAAAAAAT[-/A]AAATAAATAAAAAAT	10391
rs756408288	in-del	-/TTTT			intron-variant	CORO2B	GRCh38.p7	15:68703151	ATCTTTCTTTTTTTC[-/TTTT]TTTTTTTTTTTTTTT	10391
rs756409753	snp	C/T	4.99388e-05	0.00499669	intron-variant	CORO2B	GRCh38.p7	15:68711537	CCATGCATCTGCCCT[C/T]GCAGGTCCTCATCTG	10391
rs756434765	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68617899	TGAATCTTAGGCTAC[C/T]GGAATGCCCTAGTAA	10391
rs756503894	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68574921	GCATGGCCTAAAGCA[C/T]TGAGGCATGAAAGTG	10391
rs756541407	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68700122	AGCACCTGAGGCATC[A/G]GCCACCGAGGCCCTC	10391
rs756555238	snp	C/T	3.32574e-05	0.00407769	synonymous-codon	CORO2B	GRCh38.p7	15:68725953	ACTGAAAAACTTGCG[C/T]AACAGCCCCAAGAAC	10391
rs756576466	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68718459	CCAATTCTAAAGGGT[C/G]CAATTCTAAAGCACG	10391
rs756579112	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68595743	CTCAGTGGACACACA[G/T]AGGGGACCAATTTCC	10391
rs756600843	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727577	CAGGGCTACCCAAGC[C/T]CCTCCAGGTGAGCTG	10391
rs756611518	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68705559	TCTGTGGGATATTTA[C/T]TCATCTGAGTCCCTC	10391
rs756622182	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68676891	CCCTCCCACATCAGC[A/C]TCCCCAAGTAGCTGG	10391
rs756653600	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68614140	TCTGGGAGTGGTCCC[G/T]AGAATATATGTCTCT	10391
rs756683724	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564236	GCATTCCAATTATGC[A/G]GTGGGCTCTGGCATA	10391
rs756684019	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68724739	GCAATTACAATAACA[A/G]ATGTAATTCACACCA	10391
rs756697267	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68605918	TTAGTAGAGACGGGG[C/G]TTTCACCATGTTGGT	10391
rs756704125	snp	C/T	1.65652e-05	0.0028779	missense	CORO2B	GRCh38.p7	15:68645335	GCGCAGGGGGCGGCT[C/T]CTTCCTCGTCATCCC	10391
rs756708268	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68675813	AAATTTTTACTGAGC[A/C]CCTTCTCTGTACCCG	10391
rs756709887	in-del	-/CC			intron-variant	CORO2B	GRCh38.p7	15:68689120	AGTTCTGTCCCAGCA[-/CC]CCAAGAAGGGCTGGA	10391
rs756712033	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68570722	TTAGGGAAGGAAAGG[C/G]TCTGTGTTCAAACAG	10391
rs756739549	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625314	GTATAATTTACATGC[A/G]TTAAAAAAACATCTT	10391
rs756753941	snp	C/T	3.33028e-05	0.00408048	intron-variant	CORO2B	GRCh38.p7	15:68714050	GGACCAGGTCAGCCA[C/T]GGGGAGGCCTGCTGG	10391
rs756800353	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68654581	CTTTGGAAGTTGTAG[C/T]TCCACCCCTTAGCTG	10391
rs756801424	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68696457	GGAAGGCTGAGGCAG[A/G]AGAATCACTTGAACC	10391
rs756813875	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68612862	GGTGACAGTATCTGG[C/T]TTGTAACTGACCCCA	10391
rs756844385	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68684798	GCAAATGTGAGTTGG[A/G]GGCAAAGCCTCCTTC	10391
rs756867515	snp	C/T	3.32392e-05	0.00407658	intron-variant	CORO2B	GRCh38.p7	15:68725837	CCCTCTCTTCCTCCA[C/T]CCCAGCTCCTTCGAA	10391
rs756874582	snp	A/G	1.65754e-05	0.00287879	intron-variant	CORO2B	GRCh38.p7	15:68714698	GGCCCGGGGCAGCCT[A/G]TGGGAGAGCCCTACC	10391
rs756885827	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68641764	GAGTTCGGCACTGTC[A/G]CCCAGGTGGTAGTGC	10391
rs756911883	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68572081	GCATCTGGGAAGGGG[C/G]TGTGGGCTGTCAGTG	10391
rs756918363	snp	A/C	1.65861e-05	0.00287972	intron-variant	CORO2B	GRCh38.p7	15:68714520	GAGGGGTATGCCATC[A/C]TGCCTGCAGAGAGGC	10391
rs756926338	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68561345	CAGTGCCTGCAGCTC[A/G]CTCTCCCCGGTCCAG	10391
rs756935135	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68591791	GGCTGCCAGATGGTT[C/T]GATCTAAGGGTTGAG	10391
rs756951780	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68654673	CATGTTTCTCAGGGT[G/T]CTGTGATGATTAAAT	10391
rs756963833	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68563424	CCTAGGAGGTTGAGG[A/C]TGTGGTGAGCCTTGA	10391
rs756964492	snp	C/T	1.65026e-05	0.00287246	missense	CORO2B	GRCh38.p7	15:68645308	CCCGCTTCCTGGCCA[C/T]CGTCACCGAGAGCGC	10391
rs756996964	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68632777	TTGTATTTTTAGTAG[A/G]GATGGGGTTTTGCCA	10391
rs756999740	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68628806	GGACTCACCCAGCCT[C/T]TCCATTCATTCCCTG	10391
rs757025151	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68602957	TGGACACACAGCTTT[A/G]CAATCCCTTGCCTAG	10391
rs757040618	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68621187	AGCGTCTAATGAGCA[A/G]TTGAGCATCTTGGAG	10391
rs757059205	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564760	GTAAACGGTCAAATC[A/G]TATCAATGTTCTCCA	10391
rs757068342	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68673697	CAAAAATTAGCCAGG[C/T]GTGGTGGCATGCGCC	10391
rs757073575	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68592965	TAAAGAACAGAAGTT[C/T]ATTTGGCTCATGGTT	10391
rs757086469	snp	C/T			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632061	AGGCCTCCCAGGCTC[C/T]CAGGCCTCTCAGATG	10391
rs757125818	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566858	GCTACCAAACACAGC[A/G]TCATGTGCAACACAC	10391
rs757136123	snp	C/T	0.000148541	0.00861674	intron-variant	CORO2B	GRCh38.p7	15:68719119	AGCCCCCCATGTGTC[C/T]TCTCTTCTGCTCCTC	10391
rs757142134	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68581011	AGTCTGTCTCAATCT[A/G]TGGCCAGTGATCTTT	10391
rs757155030	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68720910	TTTTTGTTTTGAGAC[A/G]GAGTCTCACTCTGTT	10391
rs757206042	in-del	-/TGGA			intron-variant	CORO2B	GRCh38.p7	15:68697191	GGATGGATGGATTGT[-/TGGA]TGGATGGATGGATGG	10391
rs757208908	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68605029	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	10391
rs757222946	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68649262	AACTTTATTTGTTCA[C/T]GTGCTGTAATATATT	10391
rs757230461	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68608631	TGTGGGTCAGGGAAC[A/G]TACTCCCCTCTGCTT	10391
rs757231305	snp	C/G	1.65641e-05	0.00287781	intron-variant	CORO2B	GRCh38.p7	15:68719261	GGGGGCTCCACAGAG[C/G]ACAGGCGGCTGCAGC	10391
rs757264823	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68670300	CCACCTCAGCCTCCC[A/G]AGTAGCTGGGACTTC	10391
rs757270101	snp	C/T	2.50053e-05	0.00353582	intron-variant	CORO2B	GRCh38.p7	15:68710916	CTGGGTGGAGAGGGA[C/T]TGGGGAAGAGAAAGG	10391
rs757288130	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68685005	AGCACACAGTGAGGG[A/G]AAGTGATGATAGGGG	10391
rs757290512	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68663374	GCATAACTGTGGACA[C/T]GCTTTATTTCATGTG	10391
rs757292409	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68704193	TGCAGTGAGCCAAGA[C/T]TGCACCACTGCACTC	10391
rs757323580	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68691485	AAAAAATTAGCCGGG[C/T]GTAGTGGCGGGCGCC	10391
rs757323891	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68695538	ATTAAGCGTGTGATT[A/C]AGCATTTGTCTATGC	10391
rs757341956	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68657286	CTTTGGGAGGCCAAG[G/T]TGGAAGGATTGCTTG	10391
rs757361874	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68698008	GCTGGTGTCACCAGC[C/T]AGCAGGTAGTAGCCC	10391
rs757362550	snp	A/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639825	ACCAATATGTCCCAG[A/T]CTTGCGCCTTGTGCT	10391
rs757369382	snp	A/G	3.32187e-05	0.00407532	missense	CORO2B	GRCh38.p7	15:68711542	CATCTGCCCTCGCAG[A/G]TCCTCATCTGGAACC	10391
rs757379365	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68712720	TCTGCACATCATCTC[A/G]TTTAATCCTCAGGAC	10391
rs757384536	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68658258	CCTGGACCAGGGAGA[C/G]GGAACAGCTGGGGCC	10391
rs757408200	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68629404	GAGGCGCCTTTCTCT[A/G]TTCTCACAAACGTGC	10391
rs757434264	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68644675	AGTGGATGGGGGGTT[C/G]CCTTCTTGCACGTGG	10391
rs757492158	in-del	-/TTTT			intron-variant	CORO2B	GRCh38.p7	15:68709460	GATTTTTTTTTCGTG[-/TTTT]TTTTTTTTTTTTTTT	10391
rs757501665	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68680113	GTGGCTATCCCTAAG[A/G]GGCAAGGCAGAGTGG	10391
rs757537463	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68625631	TTTTTTTGAGACAGG[G/T]TCTTGCTTTGTCTCC	10391
rs757594532	in-del	-/TG			intron-variant	CORO2B	GRCh38.p7	15:68629821	GGCTCTTAACCAGCA[-/TG]TGTGTGTGTGTGTGT	10391
rs757600885	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727207	TCCGTATAGCACTTT[A/G]AAGTTTCTGCAGTCC	10391
rs757603412	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68677063	ACAGGCATGAGCCAC[A/G]GTGCCCAGTCCAAGA	10391
rs757604819	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68618041	AGTACCTGCCCTCCA[C/G]GAACCCAGTTAGTGC	10391
rs757606909	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68723936	GTAGGCCGGGGTGGT[A/G]GCTCACACCTGCAAT	10391
rs757705679	snp	A/G	1.65954e-05	0.00288053	intron-variant	CORO2B	GRCh38.p7	15:68695280	AGGGGTGCTCCCGGA[A/G]GAGGGTGGGCTCAGG	10391
rs757713887	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68719824	AACTCATTTCAGAAC[A/G]TTGCTGTCATTTGGA	10391
rs757726218	in-del	-/CAAAAAAAAAAAAA			intron-variant	CORO2B	GRCh38.p7	15:68686899	AGCGAAACTCCGTCT[-/CAAAAAAAAAAAAA]GAAAATAAAAAAATG	10391
rs757729687	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68619561	AAATGGCTCTCTCTC[C/T]CTCTGCTTCTCAAAA	10391
rs757731995	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68564414	GCTCAAGCGATCCTC[C/T]CCCATCAGCCTCTCG	10391
rs757732221	in-del	-/GCATGATCCACT			intron-variant	CORO2B	GRCh38.p7	15:68685093	CATCTGCTGGGTTCA[-/GCATGATCCACT]GCCCTCGGTACTCCT	10391
rs757737229	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68585210	CCCCTCTATTTAGGG[A/T]CGGATAAACAGAGTG	10391
rs757765564	snp	A/C	1.65108e-05	0.00287317	missense	CORO2B	GRCh38.p7	15:68695153	AGACAGGCAGGATTG[A/C]ACCCAACTACCCCAA	10391
rs757791794	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68603738	CAAACCAGGAAGAGA[G/T]GCCTCACCAGAAACC	10391
rs757810977	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68635820	CGGGACTCTTGTAGG[C/T]CTTGAGGCAAAGAGT	10391
rs757820795	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68624586	TCAAATCACCTTGGG[A/G]GCTTTTTAAACATCA	10391
rs757859991	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726343	TTGGACTTTTCCCCT[A/G]TGAAGGGGGCTGCCA	10391
rs757947225	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68594506	GAACACTAATTCCTT[A/G]GGCAGGGTGGTCCCT	10391
rs757977046	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68642931	TGGAAACTGTGGCAT[C/T]GAGAATGTTCTGCAT	10391
rs757982462	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68675451	CTAGGCAGAGGAGGG[G/T]TATCCTGTGTCTGGA	10391
rs757993477	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68655776	TCTGTCCACAAAGGG[C/T]GGCCATCCCCAAGCC	10391
rs757996325	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68654991	GGTGGTGCAGGGTCT[C/G]CAGGGAGGCATGACT	10391
rs757997272	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68641976	TCAAGCGATCTGTCC[A/G]CCTCAGCCTCCCGAG	10391
rs758015510	in-del	-/TTTTTTTTTTTTTTTTTTTTT			intron-variant	CORO2B	GRCh38.p7	15:68701483	CGCCCGGCTAATTTT[-/TTTTTTTTTTTTTTTTTTTTT]GAGACGGAGTTTCGC	10391
rs758026279	snp	C/T	1.66341e-05	0.00288388	intron-variant	CORO2B	GRCh38.p7	15:68714712	TGTGGGAGAGCCCTA[C/T]CCTCAATGCACCCCT	10391
rs758072501	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68674161	CTTGGATGTGGCTGA[A/G]AGTAGCGCAGCCACC	10391
rs758086395	snp	C/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630313	GGTCATTGTTATCAT[C/G]CCCTGAGCTGTGCAA	10391
rs758091826	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68632600	TTTTTAATTTTTGTG[-/T]TTTTTTTGGAGACAG	10391
rs758095908	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68685097	TGCTGGGTTCAGCAT[C/G]ATCCACTGCCCTCGG	10391
rs758110758	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68632833	CTGACCTCAAGTGAT[C/T]TGCCCGCCTTGGTCC	10391
rs758111798	snp	C/T	3.30256e-05	0.00406346	synonymous-codon	CORO2B	GRCh38.p7	15:68645315	CCTGGCCATCGTCAC[C/T]GAGAGCGCAGGGGGC	10391
rs758125726	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68610282	TAGCGCCTCGCCTCG[C/T]TTACAAAGCAAATGG	10391
rs758128384	snp	A/G	3.32502e-05	0.00407725	intron-variant	CORO2B	GRCh38.p7	15:68695100	ACCCCAGGGCCATCA[A/G]ACTAATCTCCTTCTC	10391
rs758137370	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68604441	TTGCCATCACTGAGG[A/G]TAGCCCTAAGAATGC	10391
rs758173625	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68705268	CATGGCGAAACCTTA[G/T]CTCTACTAAAAATAC	10391
rs758220401	in-del	-/AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA			intron-variant	CORO2B	GRCh38.p7	15:68650357	AGCGAAACTCTGTCT[lengthTooLong]AAAAAAAAAAAAAAA	10391
rs758226191	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68582331	AAGAGAAGAAAGCCA[C/G]AAAAAGGGAAGAAAG	10391
rs758235997	in-del	-/AGCAAGGGGCC			intron-variant	CORO2B	GRCh38.p7	15:68607093	GTAGGTGGAGGGGTT[-/AGCAAGGGGCC]AGCAAGGGGCCTCAA	10391
rs758240353	snp	A/G	3.31389e-05	0.00407042	intron-variant	CORO2B	GRCh38.p7	15:68719269	CACAGAGCACAGGCG[A/G]CTGCAGCCTTTGCCT	10391
rs758250644	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68662613	TATACATGGAGATGA[G/T]TAGCCTCACATGCAT	10391
rs758261663	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68557486	AGTCTATCCAAGGTC[A/G]TGGCAGAGCTGAGGT	10391
rs758272600	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68686118	CCTTGGCTCATTGCA[A/G]CCTTCACCTCCCGAG	10391
rs758280291	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68568314	TCTCATCTGTAAAGT[C/T]GGAGCGGTTATAAGG	10391
rs758286058	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68721944	TTTTTGTAGAGACAG[C/G]GTCTTACTATATTGC	10391
rs758309120	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652212	CCCAGGTCTCTTATT[C/T]GGGCTGCCGTTGTGA	10391
rs758316541	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68692729	ACCCTCGCCTCCTAG[A/G]TTCAAGTGATTCTCA	10391
rs758323811	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68583708	CCAGTTCCCTGACGC[A/G]GAATCTAGGTACCCA	10391
rs758328056	snp	C/T	0.000182504	0.00955086	intron-variant	CORO2B	GRCh38.p7	15:68719408	GTTTCCCTTGCCTTC[C/T]TTAGATCCCGTGCTG	10391
rs758351244	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68682004	CCGGAGGGCCCAGTC[A/C]CAGCCCACCCTGGGT	10391
rs758374401	snp	C/T	1.65111e-05	0.0028732	missense	CORO2B	GRCh38.p7	15:68711671	AAGGACAAGAAGCTG[C/T]GTGTGATTGAGCCCC	10391
rs758376176	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68659646	TCATTATAAAAGTCT[A/G]TCCTCGGCCAGACAT	10391
rs758392056	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600111	AGATACTTGCAGATG[A/G]ATGATCCCACAGCCT	10391
rs758404597	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68569126	TTACAATCGATGAAT[C/G]TACATTAGCATGTCA	10391
rs758418759	in-del	-/AAAAC			intron-variant	CORO2B	GRCh38.p7	15:68563003	AAAAAGAAAGAAAAG[-/AAAAC]AAAAACGTAATATAC	10391
rs758440612	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68619714	ACATATGTGTACCCA[A/T]ACATATATGTACATG	10391
rs758469060	snp	A/G			downstream-variant-500B	CORO2B	GRCh38.p7	15:68728034	GTAAGATATTTAGCA[A/G]TATCCCTGGCTCCAC	10391
rs758495113	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68678343	TCCCCTCCCTCACAC[G/T]GAGCCCCCAGAAGGG	10391
rs758525466	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68580824	ATTAACTCAGCGCCT[-/C]CCCCTGTGTCTCTTT	10391
rs758530472	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630258	GGTGGTCGTGTGCAA[C/T]GGGCAGCATGAACTT	10391
rs758573424	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618118	TTTTGTTGTGACCCA[A/G]TACACACACATGCAT	10391
rs758587997	in-del	-/TAT			intron-variant	CORO2B	GRCh38.p7	15:68725459	GTATTATTATACATC[-/TAT]TATTATGTATTATTA	10391
rs758604282	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68671582	TGCGTTAAAGCTGTC[A/G]GCCAGGGCTGCAGTC	10391
rs758624099	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577993	CTTGGAGAACCCCTC[C/T]GCTTCCACCTCTGCT	10391
rs758628203	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68661141	CGCCACCATGCCCAG[C/T]TAATTTTTGTATTTT	10391
rs758639894	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68585402	TTATTAAGCAGGCGT[C/T]GGGCACGCATGATCG	10391
rs758653647	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68564468	GCCACTACAACCGGC[A/T]AATTTATTTTATTTT	10391
rs758659060	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68719955	CACTTCCAGTCTTTG[A/T]GGAAGAGACTGGGTG	10391
rs758688315	snp	C/T			downstream-variant-500B	CORO2B	GRCh38.p7	15:68728234	ACATTGGAACGGTGC[C/T]TTGAAGTTTATCAGG	10391
rs758751367	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68606912	TCAATATATCCTCCA[C/T]TGACTGTGGATTGAC	10391
rs758774312	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68637111	ATACATGCCTTCACG[A/G]CACACTCCTCACATG	10391
rs758804039	snp	C/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641317	TGCTAGCTGGGCTGT[C/G]GGGGCAACAGGAGAT	10391
rs758805935	snp	A/G	0.00016621	0.00911467	intron-variant	CORO2B	GRCh38.p7	15:68695295	GGAGGGTGGGCTCAG[A/G]CCCCTCCCTGCTTCC	10391
rs758837711	snp	A/G	3.31455e-05	0.00407083	missense	CORO2B	GRCh38.p7	15:68718755	TGTTCCGCTTCTACA[A/G]GCTGGTGACTCTCAA	10391
rs758897752	snp	A/G	2.07497e-05	0.00322093	missense	CORO2B	GRCh38.p7	15:68710753	ATCTGGGAGATCCCC[A/G]AGGGCGGGCTGAAGC	10391
rs758936014	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654699	TAAATAAGGTGCTGT[A/G]AAAAGCACTTAGCAC	10391
rs758947530	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68586110	GCTGTGTATTCTTGG[G/T]CAAGTTGCCTCACCT	10391
rs758947703	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68696667	GTAGGGTCAGAGGGC[G/T]CTGGCAGTGGCCTTC	10391
rs758954900	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68626713	GCCCCATCATCAAGT[C/G]CATTTCGTTGGCTGG	10391
rs758966424	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658779	TGCTGACTCAGTGCC[A/G]TGGGCCTGTCCAAAG	10391
rs758985750	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68619293	CACTTTCCTTTAGCC[C/T]GAATTTTATCACTTA	10391
rs758994376	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68614327	GCAAAAGGAAGGTGC[C/T]GTATTATCACATAAA	10391
rs758995711	snp	A/G	1.71737e-05	0.00293028	intron-variant	CORO2B	GRCh38.p7	15:68719588	CCTCCACAGGCCCTG[A/G]AAGAGCAAGACCTTT	10391
rs759005660	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68692691	CAGACTGGAGTGCAG[C/T]GGTGTGATATCAGCT	10391
rs759029293	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727500	TAGGATCTACTAGAT[A/G]CATTATACTCCATAC	10391
rs759043362	snp	C/T	0.000116693	0.00763759	intron-variant	CORO2B	GRCh38.p7	15:68715354	GGTGTGCTCATGGCA[C/T]GGGAGGACATCTGGC	10391
rs759051655	in-del	-/AT	1.70003e-05	0.00291545	frameshift-variant	CORO2B	GRCh38.p7	15:68718703	CCTGTTACAGGGGTC[-/AT]GCCCAAGCACGGGCT	10391
rs759068471	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68677841	CTTCACCATAGCTGG[A/G]TGGCCAAGTCCCCTC	10391
rs759075618	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68617754	CAGGGACTAAGCCAT[A/G]CTATGCTCTTCCACT	10391
rs759084887	snp	A/G/T	3.33201e-05	0.00408156	missense	CORO2B	GRCh38.p7	15:68718727	CACGGGCTGGATGTG[A/G/T]CAGCCTGCGAGGTGT	10391
rs759086954	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68596883	GCCACCCCAGCCACT[A/C]TGGCCTCCTGACCTG	10391
rs759089519	in-del	-/CT			intron-variant	CORO2B	GRCh38.p7	15:68696101	TAAAAAAAAAAAAAA[-/CT]AGGTGGGTGTGGTGG	10391
rs759115108	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68629946	CCAGGAATCCAAAAG[C/G]ATAGGTAATGCCCCT	10391
rs759164427	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68646960	CAGCTCCATCCATCC[A/G]GGCCTGCAGGTCCCC	10391
rs759174752	snp	G/T	2.5136e-05	0.00354505	intron-variant	CORO2B	GRCh38.p7	15:68710727	ACCCTCATCTCCCTC[G/T]GCAGGTGCGGATCTG	10391
rs759185701	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591409	GGAAATGGAGGGGCT[A/G]TATGTGGCTGGACAG	10391
rs759185825	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68687575	AGTGCATGCCACACA[C/T]ACACACTGAAATGCA	10391
rs759235938	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630146	CTCGTGGCTTCTGTA[A/G]CAATGACAGCATTCA	10391
rs759259226	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68664412	CAGCACTTTGGGAGG[A/C]CAAGACAGGCGGATC	10391
rs759278560	in-del	-/GT			intron-variant	CORO2B	GRCh38.p7	15:68619756	AGTGCGTGCATGCGT[-/GT]GTGTGTGTGTGCACG	10391
rs759333923	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68624961	GCTGAGATTACAGGC[A/G]TGAGCCACTGCACCC	10391
rs759364405	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68637206	GAAATGGCACAGTCC[A/G]TGCACCTCCCATTGT	10391
rs759371057	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68666144	GGTATTAACAGCTTG[A/C]TGTACTTCTCAAAGC	10391
rs759385927	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725279	GAGGCTGAGGCAGGA[A/G]AATTGTTTGAACCCA	10391
rs759387505	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678710	AAGAAGGCAGCTGAG[C/T]GTGTCCAGGGATCAG	10391
rs759394054	snp	C/G	1.65803e-05	0.00287922	missense	CORO2B	GRCh38.p7	15:68725894	CGACGGTTGAAAGAG[C/G]AGCTGGCCCAGAAGG	10391
rs759394751	in-del	-/AAAA			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577725	GACTACTCCGGTCTC[-/AAAA]AAAAAAAAAAAAAAA	10391
rs759424416	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68611452	CCTTTTGCCTTTGAT[A/C]TTACAACATGGCATC	10391
rs759426907	in-del	-/TTCTTTTTTT			intron-variant	CORO2B	GRCh38.p7	15:68723114	AAAATGATACATACA[-/TTCTTTTTTT]TTTTTTTTTTTTTTT	10391
rs759450503	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640012	CTGGGCACCTCCCCC[A/G]GTTACAGCCTCGGCA	10391
rs759453814	snp	C/T	1.66438e-05	0.00288472	intron-variant	CORO2B	GRCh38.p7	15:68725820	CTGGGCCCTCCTTGG[C/T]CCCCTCTCTTCCTCC	10391
rs759456202	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68652661	CCACCACAGTAGTGT[A/G]GCCTGAGGAGCTTTT	10391
rs759463534	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68622146	AGAATTAAATGAGAC[A/G]AAGTTGGAGAAGGAC	10391
rs759484595	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68671877	TGGGAGGGGACTACA[C/G]AAGGCATGTATACTA	10391
rs759490106	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68593530	GGAGCCTCGTTCTCT[A/C]GACACTTGTGACTGA	10391
rs759514169	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68588947	ATTCCGAGAAATTTG[A/G]AATTCTGGGAAAGGG	10391
rs759515203	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68654164	TTTCCTTTTTTGGAA[G/T]AATGGCTGCTGATTT	10391
rs759543725	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68633734	TTGGGGCACTGAGAG[A/T]TGGGCTTCCTTTTAC	10391
rs759546295	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68571794	TCAAGAAGAGACCCT[A/G]GCAACCAAAGCCTGC	10391
rs759547337	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68674832	CTCAGACCTGCCTTC[A/G]GGAATATTCTCAAAG	10391
rs759568357	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68655679	TTGCATTTGGTTAAG[A/G]TTAGGGTGAGATTTA	10391
rs759569701	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68643895	TGCAAAAATTAGCTG[G/T]GCGTGGTGGTGGGCC	10391
rs759573405	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68613863	TCATCTTGACTTAGC[A/T]CCAGTGTCCAACTGC	10391
rs759601789	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68626106	TAAATCTTTCTGCAC[A/G]GGCTGCTTCAAAAGT	10391
rs759675637	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68611606	TTTCCTAGATGGATG[-/T]AAAATAATGGTCAGT	10391
rs759694487	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68581983	AGGTATGGACTGCAG[G/T]AGCTCTGAGCTCAGA	10391
rs759702617	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68692328	ATTCAGCTGGGCGCA[A/G]TGGCACACGGCTTTG	10391
rs759728334	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68626755	GTGTCAGTACTTATG[-/A]AAAAAACGTCTCCAC	10391
rs759743827	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68684759	ACTAATTAAGATAAT[G/T]TCTGTGCAAGTGTTG	10391
rs759752310	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68567855	TGAAACCCCGTCTCT[A/G]CTAAAAATATAAAAA	10391
rs759769730	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68667742	AAGATGGGCGGGGGG[A/T]TGTGGAGGAATGCTG	10391
rs759773030	snp	C/T	3.2981e-05	0.00406071	synonymous-codon	CORO2B	GRCh38.p7	15:68645285	CAACCACTTCTGTGC[C/T]GTCAACACCCGCTTC	10391
rs759784490	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68663083	TGTGGATAAATGGAC[C/T]CAAACAATTCAAACC	10391
rs759820229	snp	C/T	1.65179e-05	0.00287379	intron-variant	CORO2B	GRCh38.p7	15:68719098	AAGAGTAGGGGCTTT[C/T]CCAGCAGCCCCCCAT	10391
rs759829608	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68705115	GGTCAAGCAGAGCCC[A/G]TCTCCTTCTCCCAGT	10391
rs759859165	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68623113	GAGGTTGCAGTGAGC[C/T]GAGATCACGCTACTG	10391
rs759868232	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68722574	TGAATTACACCTCAC[A/T]AAAGCGGTTTTTTTG	10391
rs759884091	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68650560	GAAGTTGTAGTGAGC[C/T]GAAATCGCGCAACTG	10391
rs759933263	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68666623	CCCTCCTCCCCTGAA[-/T]TGAGCTCTTCCTGGA	10391
rs759935942	snp	A/C	1.78439e-05	0.00298691	intron-variant	CORO2B	GRCh38.p7	15:68711528	CCCTGCCTCCCATGC[A/C]TCTGCCCTCGCAGGT	10391
rs759940192	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68568929	ACCAACATGGTACAC[A/G]TTTACCTATGTAACA	10391
rs759960466	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68601537	CTAGGATGAGGGTGC[C/T]TGTGGGGGCCTGGAG	10391
rs759986247	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68651947	ACTACAAACAACAAC[C/G]GCGAAGATGCTTTGC	10391
rs759987320	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68669781	AATAAATAAGGCTGG[G/T]TGTGGTGGCTCATGC	10391
rs760124487	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597288	GGATTTTAATTCACC[A/G]GCAACAAAATACTAA	10391
rs760138852	snp	A/G	3.66663e-05	0.00428157	intron-variant	CORO2B	GRCh38.p7	15:68718837	TGGGCTGGGCTCCAG[A/G]AGGGGGGCCTGCATC	10391
rs760180049	snp	C/G	2.22437e-05	0.00333487	missense	CORO2B	GRCh38.p7	15:68710742	TGCAGGTGCGGATCT[C/G]GGAGATCCCCGAGGG	10391
rs760221036	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68635682	GTCAGGACCACATGG[A/G]GGAAAAGTTGGGCCC	10391
rs760225918	snp	C/T	2.02349e-05	0.00318073	missense	CORO2B	GRCh38.p7	15:68710826	GGCGTGTGGGGCTGG[C/T]CGAGTGGCACCCCAC	10391
rs760239890	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678774	CTGCCCACACCATGT[C/T]CCCTGGGAGCCCCAA	10391
rs760265563	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68708475	ACACCATTCTCCTGC[C/T]TCAGCAGCCCAAGTG	10391
rs760311113	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68565133	ACAAATATTGCTTTA[C/T]TGTCTACTGAACATG	10391
rs760328717	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68598335	AACTGCTGTGTGTGT[A/G]CACGTAAGCGTGTGC	10391
rs760351398	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68707484	AGTGAACAGAACTTA[A/G]ATGTCAATTAATAGA	10391
rs760364527	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68680277	CAGAGGGTGTAAGAA[A/G]CATGTCTGTACCACT	10391
rs760386954	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640336	AAAGCCAAGTAACTG[A/G]TAATGGAGACATAGT	10391
rs760390035	in-del	-/G	0.000281415	0.0118587	intron-variant	CORO2B	GRCh38.p7	15:68719245	CCGAGGTACCACAGC[-/G]GGGGGCTCCACAGAG	10391
rs760416261	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68626503	CAGACAGGTGTTCTC[C/G]CCTGGGCCCTTTGAG	10391
rs760434154	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68566350	CCACACAGCTAGAGA[C/G]TAGGAGAAGCAGGAT	10391
rs760450184	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625257	AGAATGGAGACAAAC[A/G]TGTCTTCAGCTAATT	10391
rs760495846	in-del	-/CTCCCT			intron-variant	CORO2B	GRCh38.p7	15:68593364	ATGAAATAGTTGGTC[-/CTCCCT]CTCCCTGTCCTCCTT	10391
rs760517384	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68655213	ACAAATCTGAGCTAT[A/G]TTTCTTCTATTATTA	10391
rs760530956	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68697407	GTAAATTAATATAGT[C/T]CATCTAATCAGTTAT	10391
rs760531821	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68667735	TGCACTGAAGATGGG[C/T]GGGGGGATGTGGAGG	10391
rs760594128	snp	A/G	1.64838e-05	0.00287083	intron-variant	CORO2B	GRCh38.p7	15:68715208	ACTCCATCTCTCCTG[A/G]CCCCAGGGTGATGGA	10391
rs760635783	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68592845	GGTGGTTCTCAACCC[C/T]GGCTGCAAATCACCT	10391
rs760657633	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68642752	AGGGAGAGGCGCCGG[C/T]TGTCTGCGGATTCTG	10391
rs760670062	snp	C/T	1.64917e-05	0.00287151	synonymous-codon	CORO2B	GRCh38.p7	15:68645294	CTGTGCCGTCAACAC[C/T]CGCTTCCTGGCCATC	10391
rs760677100	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68716071	CAGCTTCAGGAACAT[C/T]GGGGCTGAAAGGGCC	10391
rs760686563	snp	C/T	5.08014e-05	0.00503965	intron-variant	CORO2B	GRCh38.p7	15:68645376	GTAGGTGGCCCCTAC[C/T]TTCACTCCAGCTGCA	10391
rs760687842	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68663133	TCTTTTTTACACGAA[G/T]ATCACCAACTACCTA	10391
rs760688333	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68611370	GTACCACCCTTTGCA[C/T]TGGGTGTTTTCCTTT	10391
rs760691322	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68624057	AAAGGACTGGGGTGG[C/T]GGGTCCTGCTGTCTT	10391
rs760701115	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634313	TAGGCCCAGCTCTTT[C/T]ACTCACTCGCTGGCC	10391
rs760707404	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68582989	AGGAGAGGGAGTGTG[G/T]GAAAAGAGAAGACCT	10391
rs760734093	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68693684	TTGTGGACTCACCCC[C/T]TCCCAGGAAGTCATG	10391
rs760759117	snp	C/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616443	GAAGGTCTTGCTCAA[C/G]GTCACCCAGCCCCCA	10391
rs760771768	in-del	-/TCTTTTTTT			intron-variant	CORO2B	GRCh38.p7	15:68723115	AAATGATACATACAT[-/TCTTTTTTT]TTTTTTTTTTTTTTT	10391
rs760774161	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68623309	CAAGTCATTGAGACT[C/T]GCCAGAGCAATAGAG	10391
rs760808610	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68663894	ACTTGCATTTATTTT[C/T]GTGTGAATTGTTTAT	10391
rs760817076	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68558239	AAGGCATCAAACATC[C/T]CTACATCCAAGCCCA	10391
rs760829804	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68569009	TTTTAAAAAGCACAT[A/T]AAAAAAAGAAGAAAA	10391
rs760875357	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68706205	TCCCTACCTGCTGGC[A/G]CCCGACCCCACACAC	10391
rs760884088	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68682502	TACAGCTGTCAGGGC[C/T]CTAAGAGATCACATG	10391
rs760884120	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570007	CCTTGGGAAAGTTCT[C/T]ACCTGCAGAGAGAGG	10391
rs760903805	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68648723	AAGCAATTCACAGAA[C/G]GCAAAATATATATTT	10391
rs760911813	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68602324	TTTTTAAACACTCTT[A/G]GTGCTGTGGAAGGGA	10391
rs760918023	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68671306	AAGAGGAATCTTCTG[A/G]AATGTCAGGGACTGT	10391
rs760948574	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68562685	AATACTTCGAGACAA[C/T]GAAAACAGGCCAGGC	10391
rs760956425	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68612213	ATGCAGATGCATGTA[C/T]ACATTGAAAGGGTCT	10391
rs760972160	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68584191	GAGACCTCTTGCCTT[A/G]CCTGCATACTGTAAG	10391
rs760987994	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68713223	GAGCCTCAGTTTCCT[C/T]ACCCTCAAAATGGGG	10391
rs761002050	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68683337	CTCTTGTTGGTCCAG[A/T]CCCCGCGTCCCCAGC	10391
rs761007736	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652981	ACCAACACTTTATTA[C/T]ACCTCTCTGATGAGC	10391
rs761029253	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639767	ATTAAGAAAGTCCTT[C/T]CTTTTACAGAGTTCA	10391
rs761053123	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68606394	AGCATTTATTCCAAG[C/T]TCCCTGGATAATTCC	10391
rs761053701	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630043	GTTGGAAGGGAAAAG[A/G]GAGGGTGCTGGTGTT	10391
rs761056899	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68590361	TTCGGAGGCTGCCCC[A/C]CCATGCCCAGCCCTG	10391
rs761068115	snp	C/G	1.65034e-05	0.00287253	missense	CORO2B	GRCh38.p7	15:68711645	ACGGCAGCCTGCTCA[C/G]CACCACGTGCAAGGA	10391
rs761080317	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68682292	CTCTGGAGTTCGAGA[-/AG]AGAGACCAGCACCGT	10391
rs761102435	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68591272	TTCCAGCATGAGTAG[G/T]CAGAGGCAGATGAAG	10391
rs761141816	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68629348	CTGAAATCCAGTCCA[C/T]ATTCCACTCACTGAG	10391
rs761153757	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640715	TCTCAGATGCGATGA[C/T]GGTGATGTGCTAAGG	10391
rs761179515	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68702433	CTGGGTCCTCAGTTC[A/G]CCCCTCCTACCTCCC	10391
rs761214416	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68620312	AATGATGTTTGTACA[A/G]ATATTTAAATGTTAG	10391
rs761271158	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68567719	CTCCTTCAAAGTCCT[A/G]TAGAAATGTTGGCTG	10391
rs761274699	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68576388	ACATCACATGGGTTG[A/G]GGGCAGCAGATTGAT	10391
rs761276914	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68664385	GGGCATGGTGGCTCA[C/T]GCTTGTAATCCCAGC	10391
rs761280392	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68642729	GACAAGCTCTAGACT[A/G]GGAGCCCAGGGAGAG	10391
rs761313098	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68698883	GGCCCACCCCACCCA[C/T]CAAAACGTGGTGCAG	10391
rs761344396	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68636967	GAGGAGGAGTTTTCA[A/G]TTTAATTTTAATTAA	10391
rs761348953	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68599696	AGACCTTCCACCCAA[A/G]AGAGGCAGTGCCCTG	10391
rs761365787	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68617772	ATGCTCTTCCACTCA[C/T]TTCTAACAACCTCAA	10391
rs761403143	in-del	-/AGTT			intron-variant	CORO2B	GRCh38.p7	15:68558024	AGGCCTTTGGGGCAC[-/AGTT]AGGGGATCCCTTAAC	10391
rs761431273	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68627495	AGAGAGAAGAGGGCG[G/T]GCATCTCTTTGGACT	10391
rs761450281	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68588517	GCTCCCTGTGGAAGG[C/T]GAGGGAAGGTGGGTC	10391
rs761481152	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68713211	TCTTGTCCTCCTGAG[C/T]CTCAGTTTCCTCACC	10391
rs761509484	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68655579	CCCCTTCCCCAGAAT[C/T]CTTGCCCTCAGCCAC	10391
rs761511514	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668605	TGCTGAGGCCCAGGG[C/T]GGGGAGCCCCAGGGT	10391
rs761539693	in-del	-/TCC	1.65053e-05	0.0028727	cds-indel	CORO2B	GRCh38.p7	15:68719495	AAAGAAAAGAAGAGT[-/TCC]GTTGTGGTCAACGGA	10391
rs761554395	snp	A/G	9.95008e-05	0.0070527	missense	CORO2B	GRCh38.p7	15:68725916	CCCAGAAGGACATCC[A/G]CATTCGGCAGCTCCA	10391
rs761556544	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68721287	TTGCCATAAAATATG[C/T]TTGTATGCCATTGTA	10391
rs761557536	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68697521	TGGGAGAGTGGTGAG[A/G]AGGTGACTGGAAGGG	10391
rs761560835	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694148	GCTTGGTTGTGTTAT[A/G]ATGGAGGGAAGCACA	10391
rs761571660	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68687309	CTAAGCTGATTCTCT[A/G]GGTAAGAAAACATTT	10391
rs761573119	snp	A/C	1.68451e-05	0.00290211	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726003	CTGTTTTCTAAGCCG[A/C]TCTCTCCGTCGTTTC	10391
rs761590785	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722940	GGTGTGGTGGCGCAC[A/G]CCTGTAATCCCAGCT	10391
rs761608882	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68620898	AACAAAGGGTAGAAA[A/G]TCTGCTGGGGTAAAT	10391
rs761620912	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68617433	TTCTAGTCCCAGTTG[C/T]GCTACTCACCAGCTG	10391
rs761653029	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68705711	CACCAGTTACCCTGA[-/C]CCCCCCATCCCTGGG	10391
rs761660977	snp	A/C	1.64836e-05	0.0028708	splice-acceptor-variant	CORO2B	GRCh38.p7	15:68715213	ATCTCTCCTGACCCC[A/C]GGGTGATGGAAACAT	10391
rs761706091	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68656413	GGTCGTCAGGTGAGC[A/C]TGAGAGGTGGAAGGT	10391
rs761711112	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68655777	CTGTCCACAAAGGGC[A/G]GCCATCCCCAAGCCC	10391
rs761721340	snp	C/G/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726810	GGCCAGGGCCTTTCC[C/G/T]GCTGCATCAAGATGC	10391
rs761723811	snp	C/T	1.651e-05	0.0028731	missense	CORO2B	GRCh38.p7	15:68695213	ATATCAAATGGAACC[C/T]CTTCATCGACAACAT	10391
rs761741334	in-del	-/TC			intron-variant	CORO2B	GRCh38.p7	15:68695113	AAACTAATCTCCTTC[-/TC]TCTCTCTCTCTCTTT	10391
rs761754193	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68613488	GCAAAGCTTGAAGGA[A/C]CAGTCTTCAGTCCCC	10391
rs761758304	snp	A/C	1.66164e-05	0.00288235	intron-variant	CORO2B	GRCh38.p7	15:68719403	AGAGCGTTTCCCTTG[A/C]CTTCTTTAGATCCCG	10391
rs761770412	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68662351	CTGTATTTTCACAAT[A/G]AGATAAGGTATTTTG	10391
rs761785221	snp	A/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640785	GAGGAGGCAGGAGTC[A/T]TGATTTTTGCAAGTT	10391
rs761792578	snp	A/G	1.77253e-05	0.00297697	intron-variant	CORO2B	GRCh38.p7	15:68645409	TCCAGGGCAGAGAGG[A/G]GCCCTCCTTGGTCTC	10391
rs761794746	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68582181	GGTTTCTGAAGGACT[C/T]CTGCCCTAACTAGCC	10391
rs761803200	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68653143	GGCAGGGGTGGGGTC[C/G]TGGAGCAGCGGTCCA	10391
rs761823013	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68611215	TCTTGTTCCATTGTA[A/T]CCATTTGTATTTATT	10391
rs761824362	snp	A/G	0.000281884	0.0118686	intron-variant	CORO2B	GRCh38.p7	15:68715324	TAGGTAAGTGGCCCC[A/G]AGGCTGCCACAGCTG	10391
rs761833208	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601701	GTGTGTGCGAAGGCC[A/G]GAGAAGAAATGAGGG	10391
rs761839563	snp	A/C/G			intron-variant	CORO2B	GRCh38.p7	15:68563002	AAAAAAGAAAGAAAA[A/C/G]AAAACAAAAACGTAA	10391
rs761938035	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68654096	CTCAAAGAGAAAAGT[C/T]GCAACTTTATTTCAT	10391
rs761949121	in-del	-/TTG			intron-variant	CORO2B	GRCh38.p7	15:68723442	ATACATTTGGTTTCT[-/TTG]TTGTTGTTGTTTTGT	10391
rs762024900	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68570345	GCTTGCACCATCTAT[A/C]TGCATAAGGACTATT	10391
rs762047157	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68695656	GTTCTTTGCAGGCTG[C/G]GCAGGGTAAATGTAC	10391
rs762096743	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725129	ATCCCAGCACTTTGG[A/G]AGGCTGAGGTGGGTG	10391
rs762101848	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68672793	CCTTAGGTTATGAGG[C/T]AGGGACCTGCCACCC	10391
rs762130358	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68683068	TATTGAGAGGGCCCC[A/T]GGTATGGCAGAAACC	10391
rs762133516	snp	A/G			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68641562	CAGAAACTGCGGGCC[A/G]CTGAGCGCTCCACCT	10391
rs762134833	snp	C/G	1.6516e-05	0.00287362	synonymous-codon	CORO2B	GRCh38.p7	15:68713960	CAGAGTGAACCGGGT[C/G]GTGTTCCTGGGGAAC	10391
rs762149258	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68571695	AACATTCGCCCAAGG[C/G]ACTGCACAAGCTGAG	10391
rs762162754	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68647408	CAAGAAAAAGAACCC[A/G]ACCGGACACGGTGGC	10391
rs762200309	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68627506	GGCGGGCATCTCTTT[C/G]GACTCTCTTGGGGTT	10391
rs762208051	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68598466	TGATCCAAGGGCAGC[A/C]GTCCAATTTTCTCTA	10391
rs762247162	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68689676	ACACCCCCTGTACAG[A/G]AACAGTAACTTGTAC	10391
rs762324058	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68662166	ACATTTTATGAGCCA[A/G]TTTTCTTTCAAAATG	10391
rs762326197	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68703898	CAACAAAGTGCACAT[G/T]AAAAATATAACTTGG	10391
rs762350278	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68604249	ATTGCTCAGAGTTTT[G/T]GGGACCTTCCTGAGA	10391
rs762354948	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648732	ACAGAAGGCAAAATA[C/T]ATATTTTAACCTACT	10391
rs762360212	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68609416	AGAAGAGGGCTGTGG[C/T]TGTGCAGGCTTTGGG	10391
rs762392068	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68621949	TTTCTTATTATTTGT[A/G]GAGATAGGTTCTCAC	10391
rs762395637	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68616662	GCGCAAGCAGGCAAT[A/C]CCATGTCATCTGCGA	10391
rs762400989	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68720479	CCCGTGGCTGAAGGT[A/C]TCTCATGAGGGTACA	10391
rs762457980	in-del	-/CTGGG			intron-variant	CORO2B	GRCh38.p7	15:68670405	TGATCTCTTGAAATC[-/CTGGG]CTGGGCTCAAGTGAT	10391
rs762458334	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68618437	AAGTGGCACTTGAGC[C/T]GAGTCCAGATGTGTG	10391
rs762480455	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68621640	TTGGCCTTGCTTTGG[C/T]TTGGTTGTTGGTTTG	10391
rs762483637	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68627609	AGGAGACTCTGCATC[A/G]TGGTTGGGTGAGAGG	10391
rs762485341	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68588767	GGAATCTGGTAGAAT[A/C]CAGGACGTGGAACGG	10391
rs762490603	in-del	-/CTTTTC			intron-variant	CORO2B	GRCh38.p7	15:68690649	ACGTTAGCTTTCTTT[-/CTTTTC]TTTTTTTTTTTTTTT	10391
rs762492494	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68605790	TGCAGTGGCGCAATA[G/T]CTCAGCTCACTGCAA	10391
rs762506476	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68717517	CTAAGGTATCGGATA[C/T]GGAGGGGTGGAGAGG	10391
rs762531703	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68694396	GGGGAAACCGAGGCT[C/G]AGAGAAGTTCATTAA	10391
rs762532945	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68700044	GTTTGCAGCTTCCAG[G/T]GGGTGGACAGGAGGT	10391
rs762536095	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668710	TGATGTGGGAAGCCA[C/T]TGGAGGGTTTCAAGC	10391
rs762544193	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68639410	GCATTAATCAGCTCT[A/G]TGGGACACCCTAAAA	10391
rs762560637	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699083	GAGACCCAGTATATC[C/T]GGTGTGCTTGGCCTG	10391
rs762566954	snp	C/G/T	8.46627e-05	0.0065058	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726013	AGCCGATCTCTCCGT[C/G/T]GTTTCTACTCATCCC	10391
rs762590308	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68711936	CCCCACTGCACCCCC[C/T]ACCTCCAGACAGGAT	10391
rs762593003	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68563049	GGATTCATTGAAAAC[A/G]GTGGTTAGAAGGAAA	10391
rs762616328	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595430	ATACGCCTTATCGTC[A/G]GATATAGAAGCCTGT	10391
rs762619037	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68677628	AAAACCTCCATGGGC[A/G]GGAAGAAAATAGCTG	10391
rs762619498	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726828	TGCATCAAGATGCCA[A/G]TCCCTTTGTGGGCTT	10391
rs762681169	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68574579	TCCTCATTCCTTGCT[A/C]TAGGGACCTGGACTT	10391
rs762684527	snp	G/T	1.64868e-05	0.00287109	missense	CORO2B	GRCh38.p7	15:68715241	CATCCGGTACTACGA[G/T]ATCAGCACTGAGAAG	10391
rs762702573	snp	C/T	1.6593e-05	0.00288031	intron-variant	CORO2B	GRCh38.p7	15:68715328	TAAGTGGCCCCGAGG[C/T]TGCCACAGCTGGTGT	10391
rs762709225	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68663448	ATAGTTGAAGAGGTA[C/T]GTGCTTTCTTCCAGG	10391
rs762748961	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634374	GCACTTTTGAAGGTG[C/T]AGATTGACTGATAAA	10391
rs762786236	in-del	-/TG			intron-variant	CORO2B	GRCh38.p7	15:68629822	CTCTTAACCAGCATG[-/TG]TGTGTGTGTGTGTGT	10391
rs762795317	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68705938	GTACGTGAGACTGGA[A/T]CCTGGGCTGGGGCTC	10391
rs762799271	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68676477	CTGCAAGGATAACCA[C/T]CGCTGCCTAAACCCG	10391
rs762813162	in-del	-/AGG			intron-variant	CORO2B	GRCh38.p7	15:68638625	AGGTGGAGAGGCTGA[-/AGG]AGGAGAAGATATGTG	10391
rs762825703	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68664169	CAAAAATTCAATGAG[A/C]CTTACAGCTAAGATC	10391
rs762846422	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68612384	TGAGAGGAGGTGTGC[A/G]TGAGAAGGGGCAGAG	10391
rs762851734	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68718080	TGCTCCTAGCACCAC[C/T]ACACTGCCCCTCATC	10391
rs762867851	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68688224	TTTTTTAATAACAAT[G/T]TTATATGTTTGTTAG	10391
rs762871478	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68609449	AGGGCATCAGTTTGT[C/G]GTCCACATCAAGCAT	10391
rs762884578	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68590970	CGAGGACTGAGATTT[A/G]TTTAAAAAAAATTTG	10391
rs762895781	snp	C/G	1.66283e-05	0.00288338	missense	CORO2B	GRCh38.p7	15:68719539	AAAATGTCCCACCCA[C/G]GACAGAGAATGAGGT	10391
rs762902893	snp	C/T	1.6522e-05	0.00287414	synonymous-codon	CORO2B	GRCh38.p7	15:68713990	CATGAAGCGGCTCCT[C/T]ACGACAGGGGTCTCC	10391
rs762922124	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694734	ACCCAGCATCTGAGC[A/G]TGCGTGAACAAGGCA	10391
rs762951839	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68596609	CTTCTCGACTGACTG[A/G]GAGGACAGATAGGTG	10391
rs763003854	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68684422	TGATTGGGATGGAGG[C/G]AGAGAAAGAACACAG	10391
rs763092315	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68673307	TTGGAAGGCTGAGGT[A/G]GGAGGATTGCTTGAG	10391
rs763100980	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703983	CAGATCACTTGAGCT[C/T]AGGAGTTCGAGACCA	10391
rs763132946	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68654330	TGGGAGGTCAAAGAA[C/T]CCATCCCTCTCCCTT	10391
rs763144997	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68620799	CAGCTGAGGCAGGAC[A/C]AGGGCTAGAAGGTTT	10391
rs763153309	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68700805	GGCCAGCAGCCGCGG[-/AG]AGAGAGAGAGGTTTC	10391
rs763159252	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631465	CTAGTAAGTGGTGGC[A/G]CTAGGATTTAAACCT	10391
rs763171277	snp	A/C	1.64868e-05	0.00287109	missense	CORO2B	GRCh38.p7	15:68645271	AAGAATGTGCACGAC[A/C]ACCACTTCTGTGCCG	10391
rs763175034	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68561085	GTTCCCTCCACCCCG[C/T]GTCCCCCAGGCTCCC	10391
rs763210391	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68650482	CTGGGCGTGATGGTG[C/T]GTGCCTGTAATCCCA	10391
rs763213024	snp	A/G	1.67489e-05	0.00289381	intron-variant	CORO2B	GRCh38.p7	15:68714072	GCCTGCTGGGTTTGG[A/G]CTAAAGGAAGCATCG	10391
rs763301484	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68561819	GTATGAGGCCATGGT[A/T]ATCCTGCTAGTGTGC	10391
rs763344194	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68604335	AGCCCCCACCCCCAA[A/G]CCGCCTTTCCTACCA	10391
rs763348748	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68664546	CAGCTACTTGGGAGG[C/G]TGAGGCAGGAGAATG	10391
rs763350812	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68581744	AGGAGAACCCTAAAG[A/G]GGGTGTGAGAGGTAG	10391
rs763362599	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68609604	AAATGGGGTTTTCAT[C/T]TCCTCTTTGCTGCTG	10391
rs763377725	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68681127	TGAGGCAGGAGAATC[-/G]GCTTGAACCCAGAAG	10391
rs763379826	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648951	TGTATTTAAAAAATA[C/T]GTGTGCAGCATTTTT	10391
rs763389269	in-del	-/CCTCTAGCAA			intron-variant	CORO2B	GRCh38.p7	15:68702362	GACCACTTCATGCAT[-/CCTCTAGCAA]CCCCCTCCCAGGACT	10391
rs763396618	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68567702	GGAAGGCATGCCCTT[C/T]ACTCCTTCAAAGTCC	10391
rs763414219	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68661587	TAAACCTGACTACAT[A/T]TGCACAAAACAGTAG	10391
rs763436544	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68579706	AGGCCAGCGGAGGGG[A/C]AACCCCACCCCACCT	10391
rs763470803	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68657539	AAAAAAAAAAAAAGG[-/A]AATACAGTTATCAAA	10391
rs763524336	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68581773	AGGATCGCTGCTGAC[A/G]CACTGGGAGCGGTAG	10391
rs763525030	snp	A/C	1.65119e-05	0.00287327	missense	CORO2B	GRCh38.p7	15:68719202	CGGAGCCAGCACTGA[A/C]CCCGGATGAATGGCT	10391
rs763529429	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68607486	ACCCAGATTCCACTG[C/G]AGAGGACATGGAACC	10391
rs763537889	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68719677	TCTGTGACAAATGCC[A/G]TAAGTAGCCTGATAT	10391
rs763566862	snp	C/G	2.12051e-05	0.00325609	missense	CORO2B	GRCh38.p7	15:68710751	GGATCTGGGAGATCC[C/G]CGAGGGCGGGCTGAA	10391
rs763579758	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68635800	TTTGTGATCTGGAGC[G/T]CCAACGGGACTCTTG	10391
rs763579950	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68558144	CTGGGCCAGCCTGGC[A/G]GAGGGCAGATAAGAA	10391
rs763586699	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68585107	TAGCAATGGGAGGCT[C/G]CCAGGTTTGCTCAGG	10391
rs763620294	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68599754	CCCAGGCTCTCCCCT[C/G]CCCTGGGAGGCTGCC	10391
rs763648884	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68678891	CCCAGGTTACTGGAC[A/G]GATAGTGGATCTGGC	10391
rs763650638	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68664670	ACCAAAAACCAAAAA[A/C]CAAAAAAACCTGAGT	10391
rs763654318	snp	C/T	6.08748e-05	0.00551667	synonymous-codon	CORO2B	GRCh38.p7	15:68710827	GCGTGTGGGGCTGGT[C/T]GAGTGGCACCCCACC	10391
rs763692322	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68692333	GCTGGGCGCAATGGC[A/G]CACGGCTTTGGAAGG	10391
rs763699566	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68709517	CCCAGGCAGGAGTGC[A/G]GTGGATCTCAGCACA	10391
rs763744045	in-del	-/C	1.65548e-05	0.002877	intron-variant	CORO2B	GRCh38.p7	15:68719251	TACCACAGCGGGGGG[-/C]TCCACAGAGCACAGG	10391
rs763745891	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727252	TCTCATGGAGCCTCA[C/T]GTCTACTCCCTTCTG	10391
rs763753754	snp	C/T	1.66299e-05	0.00288352	intron-variant	CORO2B	GRCh38.p7	15:68725829	CCTTGGCCCCCTCTC[C/T]TCCTCCACCCCAGCT	10391
rs763765611	snp	A/T	1.65795e-05	0.00287914	missense	CORO2B	GRCh38.p7	15:68725904	AAGAGGAGCTGGCCC[A/T]GAAGGACATCCGCAT	10391
rs763783884	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68674559	CATCACCCTCTTACT[C/T]ACTGGGTGACCTCAA	10391
rs763789815	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68614135	GAATCTCTGGGAGTG[G/T]TCCCTAGAATATATG	10391
rs763828253	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68684688	TCATTCTGGTTCTGT[A/C]ACTGCCAAGTGGTGT	10391
rs763845277	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68666680	CTGTGGGCACTGGGG[A/G]TTGGGGTGTTGTGTT	10391
rs763874028	snp	G/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615769	CCAGACACCAAATCC[G/T]TCAGTGCCCTGGTCT	10391
rs763914538	snp	C/T	1.6596e-05	0.00288058	intron-variant	CORO2B	GRCh38.p7	15:68714516	TGGGGAGGGGTATGC[C/T]ATCCTGCCTGCAGAG	10391
rs763925280	snp	C/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726183	TTCTGGAGACCCCCT[C/G]CCGGCAGCCCCTTTC	10391
rs763942165	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68673559	GGAAAGTGTCTTGGC[C/T]GGGCTCCGTGGCACA	10391
rs763948862	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68654567	GGAGCCTCCCATACC[A/T]TTGGAAGTTGTAGCT	10391
rs763959067	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68632615	GTTTTTTTGGAGACA[G/T]AGTCTTGCTCTGTCA	10391
rs763962674	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68642760	GCGCCGGCTGTCTGC[G/T]GATTCTGAGAAGGTC	10391
rs763974116	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68606040	GCTCTTGGGTTTTGA[-/G]GGTGAGCAGCTGGGT	10391
rs763974715	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68592846	GTGGTTCTCAACCCC[A/G]GCTGCAAATCACCTG	10391
rs763984312	snp	A/C			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615606	GATTGGTCATTAACC[A/C]GTCACCTTTATGATA	10391
rs763994071	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68641679	GCAGCTTGGCACTGG[C/T]TCCTCCCAAGCCCTT	10391
rs764032275	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68685848	ATTACTTAAACTCCC[A/G]GGTGATTCTAAAATG	10391
rs764046863	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631871	TGAGCTGCCAGGAGG[A/G]GGTGCTCCTCGCAGT	10391
rs764074877	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68562639	ATAACTGGATCACAG[-/A]AAAATCACAAGAGAA	10391
rs764089926	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68674889	CAATATTATCTCCCA[C/T]TACACTCTCTTTAGG	10391
rs764105965	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68722692	TAGCACGTCATCCCT[C/T]TCAACAGATGTAACT	10391
rs764136413	in-del	-/GAGC			intron-variant	CORO2B	GRCh38.p7	15:68595875	GACCCTGGTGAGACG[-/GAGC]GAGCGGGCGTCTGGG	10391
rs764149370	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68612247	AGTAAATATGTGAAT[A/G]TGGAAGGATAAAGAT	10391
rs764163747	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68624098	CCTAACCTGTAATTC[C/T]GTCTCCTCATCCCAT	10391
rs764175143	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68569063	CCTGCTTCCACACAC[A/C]CACAATCTCCCCCAC	10391
rs764193408	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68681737	GGGAGCTGACTAAGT[C/T]AGGATTCCTGCTGCA	10391
rs764194979	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68716137	AACCAAAAGATGTCC[A/G]AAGTCCTAATCACCA	10391
rs764201826	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68700141	ACCGAGGCCCTCCCT[C/T]CACCCATTCCAGCTG	10391
rs764203287	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68625308	TCGAGGTATAATTTA[-/C]CATGCATTAAAAAAA	10391
rs764207955	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68583127	GCCTCAGCTCCAGCA[A/G]GGCACAGCCTGCTGA	10391
rs764224230	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68601015	AAAGGGAGAGGACAC[C/G]TCCTAGCCAGCCTTT	10391
rs764234702	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682505	AGCTGTCAGGGCTCT[A/G]AGAGATCACATGGCC	10391
rs764234801	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68561001	ATGGGAATTTAGGAG[A/G]GGCCATATTTCCCCC	10391
rs764252320	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68667905	CAGCCATTTGCTAGA[C/T]GAGTTATTACTCCCG	10391
rs764265534	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601678	TGGCTGAGGTCAAGG[A/G]AATGGCTGTGTGTGC	10391
rs764275071	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652047	ATCCCCACCTCACAC[C/T]TGGGGAAGCTGAGAC	10391
rs764282235	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68713256	AATGATTTCTTCCGA[C/T]AGATATTGTTATGGG	10391
rs764287923	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68589739	GAAAGTTCCAGAAAG[A/G]AGACTTTGAGAACTT	10391
rs764299030	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68583010	GAGAAGACCTTTCAT[G/T]CCAACATGCTCCTCC	10391
rs764348072	in-del	-/GCAA			intron-variant	CORO2B	GRCh38.p7	15:68669197	AAAGGAAGCAAGCAA[-/GCAA]GCAAGCAAGCAAGCC	10391
rs764354183	snp	A/G	0.000199644	0.0099891	intron-variant	CORO2B	GRCh38.p7	15:68719393	ATCGTCAGTGAGAGC[A/G]TTTCCCTTGCCTTCT	10391
rs764354962	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68587443	TCAGTATTTAACTCC[C/G]GAGATGTCTGAGGTC	10391
rs764370358	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68712674	GACATCTGCTAAGAG[C/T]TCACTGTGTGGCCTG	10391
rs764370419	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68724201	AGCAAGACTCTGTCT[C/G]AAAAACAAACAAATA	10391
rs764385943	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68590387	CCCTGCACTTCTGTT[C/T]TCTCAGGTACCCCCA	10391
rs764420828	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68627292	TCATCCCAACCATCA[A/G]GGAGTTTGGAGTTAG	10391
rs764434328	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639772	GAAAGTCCTTTCTTT[G/T]ACAGAGTTCAAAACC	10391
rs764436371	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648733	CAGAAGGCAAAATAT[A/G]TATTTTAACCTACTA	10391
rs764440010	snp	C/T	1.6504e-05	0.00287258	synonymous-codon	CORO2B	GRCh38.p7	15:68711646	CGGCAGCCTGCTCAC[C/T]ACCACGTGCAAGGAC	10391
rs764440552	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68558266	CCCAGCTTCTCCGGA[A/T]GCTGTCTGCTGCTGC	10391
rs764451921	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68680054	ATGGTGGGCACTGGG[-/C]CCCCGCAGAGTGTGC	10391
rs764453783	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68684291	ATAGATGACCCGCAA[-/G]GGAGAAATGGACTAA	10391
rs764453998	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699838	CCCCTCACCAGTGGC[C/T]CTGGTTCTACAAGGG	10391
rs764455002	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591315	CATTCCAGGTTGAGC[A/G]GGCAGCGTGAACAAA	10391
rs764495912	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727773	GCTGCCTCCCAAGGA[C/T]AGAATTGAAATAAAA	10391
rs764571592	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68671339	CCACAGTTTGAGACC[A/C]AGGAAAATTGGCTCA	10391
rs764573765	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600524	AGTCGGAAAGACAAA[A/G]CGGTCTTTGTTAACA	10391
rs764582480	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68697703	GGTCAGGGGTCAGGA[C/T]ATAGGCAGGCCAGGG	10391
rs764584265	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68587538	ATTTTAATTTAGATT[C/T]GTTTAAGAAATACCA	10391
rs764586966	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68573644	CTGGGTGACAAAACA[A/G]ACAGAAAGGGAGAAA	10391
rs764620044	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630046	GGAAGGGAAAAGGGA[A/G]GGTGCTGGTGTTTGC	10391
rs764706910	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68627502	AGAGGGCGGGCATCT[C/G]TTTGGACTCTCTTGG	10391
rs764795348	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68626648	TCACTGCTTCTAGAG[C/G]AGTGGCTTTTCATTC	10391
rs764823522	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68585986	CCTGGTCCAGGCCTG[A/C]AGCCCTTACGAAGCA	10391
rs764858282	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68617975	ATTTATTGAGCATCT[A/C]CTATGTCCCAAGCTT	10391
rs764891887	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68667871	AAGACCATGGGCTTC[A/G]GGACCTGTAGTCCTG	10391
rs764926266	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68684811	GGGGGCAAAGCCTCC[C/T]TCAGGCCCGGGAGCC	10391
rs764934933	snp	C/G	3.31708e-05	0.00407238	intron-variant	CORO2B	GRCh38.p7	15:68714702	CGGGGCAGCCTGTGG[C/G]AGAGCCCTACCCTCA	10391
rs764938284	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68721683	GGGTTCATGGTGCTA[A/T]ACTTTCTATTAATAT	10391
rs764943267	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68694389	TTAGAGAGGGGAAAC[C/T]GAGGCTCAGAGAAGT	10391
rs764943653	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703338	GTATTTTTAGTAAAG[A/G]CAGGGTTTCACCATG	10391
rs764964831	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68674962	AAGGAATGAATCCCT[A/G]ATAGTAGAACTTCAG	10391
rs764985227	snp	C/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726314	GGAAGCGGGATCCCA[C/G]CTAGACTTAGAACTT	10391
rs764997598	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68698979	TTAGTTTTGACCAAG[A/G]TGCAGAGAGGAGAAG	10391
rs765003321	snp	A/G	1.6659e-05	0.00288604	intron-variant	CORO2B	GRCh38.p7	15:68695091	TTCAAGGCCACCCCA[A/G]GGCCATCAAACTAAT	10391
rs765029499	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68707092	AGCCTCCTGAGTAGC[-/T]TGGGATTACAAGCGC	10391
rs765034203	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68685095	CTGCTGGGTTCAGCA[-/C]TGATCCACTGCCCTC	10391
rs765054849	snp	C/T	1.65045e-05	0.00287263	synonymous-codon	CORO2B	GRCh38.p7	15:68645309	CCGCTTCCTGGCCAT[C/T]GTCACCGAGAGCGCA	10391
rs765071895	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68567467	GAAGATAAGGGTTAC[C/T]TTGGAGAGTATTTTT	10391
rs765091210	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68662495	TGCAGTTGTCATTCA[A/G]GGTTTACACTATTGC	10391
rs765094121	snp	A/G	1.64863e-05	0.00287104	missense	CORO2B	GRCh38.p7	15:68715231	GTGATGGAAACATCC[A/G]GTACTACGAGATCAG	10391
rs765105899	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68716384	CCACATGTGCAAGGC[A/C]CCTGGCAGAGCACTT	10391
rs765111318	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68623471	CCACAGCTGTGTTTA[C/T]ACCACCTCCTCACCC	10391
rs765122753	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68594181	GCTGAGGTTTGCAGC[C/T]AGAACTCTGGTCCAC	10391
rs765166575	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68676334	GCTGCACAAACCCTC[C/T]AGAGGATTCTGAATT	10391
rs765170827	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725235	TTATCCAGGCATGGT[A/G]GCACATGCCTGTAAT	10391
rs765171613	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68704625	TCAGCTGCCTTGCCT[C/T]TGCCTTGTCTGCAGT	10391
rs765181811	in-del	-/A	1.65425e-05	0.00287593	frameshift-variant	CORO2B	GRCh38.p7	15:68719522	CGGAATAGATTTATT[-/A]GAAAATGTCCCACCC	10391
rs765207736	snp	C/T			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68641563	AGAAACTGCGGGCCG[C/T]TGAGCGCTCCACCTG	10391
rs765229247	in-del	-/GTG			intron-variant	CORO2B	GRCh38.p7	15:68609216	TGAGCATGGGGCATT[-/GTG]GTGGTGGTGGTTGGG	10391
rs765295182	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68590406	CAGGTACCCCCATAA[C/G]TCTGCTGTTACCCCC	10391
rs765301537	snp	A/G	6.62888e-05	0.00575674	missense	CORO2B	GRCh38.p7	15:68719529	GATTTATTAGAAAAT[A/G]TCCCACCCAGGACAG	10391
rs765314419	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68670318	TAGCTGGGACTTCAG[A/G]TGTGCACCACTAAGC	10391
rs765315771	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68601742	CAGAAAGAAGTTGAG[G/T]GCAGCTGGGGCTTAG	10391
rs765339051	snp	C/T	1.66128e-05	0.00288204	intron-variant	CORO2B	GRCh38.p7	15:68719404	GAGCGTTTCCCTTGC[C/T]TTCTTTAGATCCCGT	10391
rs765355857	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68683585	TCCCCCCACTGTAGG[A/T]TATTGAGACATCATG	10391
rs765367141	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68659251	GTGAGGGATAAGGGC[A/G]CTGACCCCTGCACCA	10391
rs765374763	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68562993	AGAAAAAAAAAAAAG[-/G]AAAGAAAAGAAAACA	10391
rs765375658	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68613703	CTAAATTAGCACATC[A/G]CTAAGAGTTTTTCAG	10391
rs765406888	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68649068	TAAACGCTTCCTCTC[A/G]ATTTCTGTAATGGTA	10391
rs765419609	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68702624	GAGAGAGCTCCAGGA[A/G]CCTCCTGGCCCCTAA	10391
rs765422507	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640837	AGTAGAAAGAAAGAG[A/G]AGGGCTGGGGTAGAG	10391
rs765428327	snp	A/G	4.95127e-05	0.00497533	synonymous-codon	CORO2B	GRCh38.p7	15:68711652	CCTGCTCACCACCAC[A/G]TGCAAGGACAAGAAG	10391
rs765439303	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570359	TCTGCATAAGGACTA[C/T]TGATCTGTGGTTTTC	10391
rs765495481	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68625647	TCTTGCTTTGTCTCC[C/T]AGGCTAGAGTGCAGT	10391
rs765507637	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68619679	AATGTGTGTGTGTGT[A/G]TATATATATATGTAC	10391
rs765550337	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577957	GGAAGCCAGCACTTC[C/T]GGGCTTGCCAGGCTG	10391
rs765564910	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68671490	ATAGAAAATATAGCT[A/G]TGTTAATGTTCTGTT	10391
rs765571967	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68580276	TCGGGCTTGGCCGTC[C/T]ATTCAAGGGCCAGAC	10391
rs765594336	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68689686	TACAGAAACAGTAAC[G/T]TGTACAACAGAGGCA	10391
rs765611661	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68602845	CGTGGAAGCAAGCCT[C/G]TTTCCTGGGAAAAGA	10391
rs765619228	in-del	-/AAAT			intron-variant	CORO2B	GRCh38.p7	15:68724212	GTCTCAAAAACAAAC[-/AAAT]AAATAAATAATAAAA	10391
rs765631038	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68647479	CAGATCACCTGAGGT[C/T]GAGAGTTTGAGGCTA	10391
rs765661095	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68680482	ACAGAAGGCTCTGCA[C/T]CATGCAAATGGTACC	10391
rs765665502	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68637003	ATTTAAGCAGCTGCA[C/T]GTGGCTAGTAGCTAC	10391
rs765669753	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68662544	TACATCAAGAACCTC[-/AA]GAGATCACTTTGTAT	10391
rs765672530	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68660613	TAGGCTCAAGCAATC[C/T]ACCCATCTTGGCTTC	10391
rs765673227	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68579510	TGGCCAACATCCCTC[C/G]GCGCCCGGCCCAACC	10391
rs765673646	snp	A/G	1.66109e-05	0.00288187	missense	CORO2B	GRCh38.p7	15:68718736	GATGTGTCAGCCTGC[A/G]AGGTGTTCCGCTTCT	10391
rs765694464	in-del	-/TTG			intron-variant	CORO2B	GRCh38.p7	15:68723444	CATTTGGTTTCTTTG[-/TTG]TTGTTGTTGTTTTGT	10391
rs765703762	in-del	-/TTT			intron-variant	CORO2B	GRCh38.p7	15:68686021	GAGCTCCTACTTCTG[-/TTT]TTTTTTTTTTTTTTC	10391
rs765707959	in-del	-/AAAA			intron-variant	CORO2B	GRCh38.p7	15:68576153	GTGAGACTACGTCGC[-/AAAA]AAAAAAAAAAAAAAA	10391
rs765740798	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68574729	ATAATTAGAGCCCAT[A/C]AAGAGACAGAAGCAA	10391
rs765783487	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68594511	CTAATTCCTTGGGCA[C/G]GGTGGTCCCTGCTTG	10391
rs765793508	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648766	TGGAAAAGATTTAAA[A/G]GAGTAATAATCATCA	10391
rs765830652	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68588786	GACGTGGAACGGCTG[A/T]TGGAAAGAAAGGTGT	10391
rs765855682	snp	C/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726954	GAGGCCCCTCACGCT[C/G]TGTGCCCCTAGATCC	10391
rs765880894	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68616675	ATCCCATGTCATCTG[C/T]GAGATCTCCCATGGG	10391
rs765886258	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68609450	GGGCATCAGTTTGTG[A/G]TCCACATCAAGCATC	10391
rs765945362	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68700047	TGCAGCTTCCAGGGG[A/G]TGGACAGGAGGTCAG	10391
rs765965076	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68675494	CTTGAGGAGGTAGGA[G/T]GTGAAGTTGTAAATT	10391
rs765984907	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68723527	TGGCATGATCTCGGC[C/T]CACTGCAACCTCCAC	10391
rs765996187	snp	C/T	1.66222e-05	0.00288285	intron-variant	CORO2B	GRCh38.p7	15:68715341	GGCTGCCACAGCTGG[C/T]GTGCTCATGGCACGG	10391
rs765999578	in-del	-/T/TTTCT			intron-variant	CORO2B	GRCh38.p7	15:68690646	ATCACGTTAGCTTTC[-/T/TTTCT]TTTTTTTTTTTTTTT	10391
rs766020773	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68706354	AACAGCTGGGTTCAA[A/G]CTTTCCAACAGCTCT	10391
rs766059041	snp	C/T	8.4023e-05	0.00648108	missense	CORO2B	GRCh38.p7	15:68645181	TGGCGTCCGCAATAC[C/T]GTAGCTCCAAGTTCC	10391
rs766062375	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68569523	ATGTACCACAGTTTA[C/T]TTATCTGTTCACCTA	10391
rs766073423	snp	C/G	1.65452e-05	0.00287616	intron-variant	CORO2B	GRCh38.p7	15:68695125	CTTCTCTCTCTCTCT[C/G]TTTCTCCTCTGCAGA	10391
rs766073429	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68633910	TCTTTTTCTGCATTG[C/T]CAGGTGACAGGGAGC	10391
rs766082167	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68596619	GACTGGGAGGACAGA[C/T]AGGTGAAGGATAAGG	10391
rs766082858	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68563053	TCATTGAAAACAGTG[A/G]TTAGAAGGAAATATA	10391
rs766087372	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68704780	AACAAGGCTCTGACC[C/T]AGGGACCTGTAAAGG	10391
rs766089082	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727461	AAATCAAGAAATGGG[C/T]GTCCACTCTTTTCTT	10391
rs766098440	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68644525	ACCTATGTTCATGGC[A/C]CTACTTAGCTGTGTA	10391
rs766133050	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68677741	CCCTACCAGGTTGGA[A/G]GGTTCCTCACCCACT	10391
rs766150840	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68644142	ACTCCAAAATCTTAG[C/T]GGCTTATAACAAAAG	10391
rs766159237	snp	C/G	1.65512e-05	0.00287669	missense	CORO2B	GRCh38.p7	15:68695247	TGCCTCGTGCTCGGA[C/G]GACACGTCGGTGAGC	10391
rs766169903	snp	C/T	4.96956e-05	0.00498451	synonymous-codon	CORO2B	GRCh38.p7	15:68719417	GCCTTCTTTAGATCC[C/T]GTGCTGATGTCTTTG	10391
rs766175705	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68706109	TCAAGCCTCAGTGAC[A/G]AGATATGACACACAT	10391
rs766209694	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68595475	AGCCATGCAGCAGGG[C/T]TCAGATATCCGCTGT	10391
rs766245285	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68653287	CGAAAAGGAAGCAGT[A/C]AACAAGACCAAGTCT	10391
rs766272812	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68583543	TGCTGGTGCCTGGAT[A/T]TCCCTCTGTGGGACA	10391
rs766304726	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68715984	TTCCCACCTCTGCGG[A/G]TGATCCTCTTTGGAG	10391
rs766306030	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68695664	CAGGCTGGGCAGGGT[A/G]AATGTACCATCTGGT	10391
rs766306592	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68586177	TGATAATAGTAACAA[A/T]CCTTTACTATTAAGG	10391
rs766332015	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634435	AAGCATGTTCACACA[C/T]AGTATTATTTCACTG	10391
rs766332813	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68664294	TTCCGTTGAGATTGC[A/T]ATAATTTATATTTGA	10391
rs766335301	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68632449	ACAGAAGTTGAGAAA[C/T]GTCCTCTCTCAACAA	10391
rs766363140	in-del	-/TTTC			intron-variant	CORO2B	GRCh38.p7	15:68560281	GTTCTTTTTTTTCTT[-/TTTC]TTTCTTTCTTTATTT	10391
rs766384583	in-del	-/TT			intron-variant	CORO2B	GRCh38.p7	15:68673953	AAAAGAAGGGTTGAC[-/TT]TTTCGGTGGACCCAG	10391
rs766385054	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68682541	TTGACATTCTCTGAT[C/T]GACTGGTAGGGACTC	10391
rs766408223	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68718538	CAGAGACAGAGACTG[-/A]TTGAAGGCGCCCCGG	10391
rs766429446	snp	A/G	1.67708e-05	0.00289571	intron-variant	CORO2B	GRCh38.p7	15:68714077	CTGGGTTTGGGCTAA[A/G]GGAAGCATCGTTGCC	10391
rs766445149	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578001	ACCCCTCTGCTTCCA[C/T]CTCTGCTAACTCCTC	10391
rs766445795	snp	A/G	6.76304e-05	0.00581469	missense	CORO2B	GRCh38.p7	15:68645176	TGTCCTGGCGTCCGC[A/G]ATACCGTAGCTCCAA	10391
rs766452912	snp	C/T	6.60862e-05	0.00574793	missense	CORO2B	GRCh38.p7	15:68713992	TGAAGCGGCTCCTCA[C/T]GACAGGGGTCTCCAG	10391
rs766455868	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68629625	AAGGCTATGCACTGA[A/G]CAGCTCCCAGGCCTT	10391
rs766459571	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591612	ACATTCTCAAAGCCT[A/G]TGTGCAATGAGGCGG	10391
rs766460133	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68621915	GCACATGCCACCATG[C/T]CTGGCTAATTTTTCT	10391
rs766463288	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68620893	CCCCCAACAAAGGGT[A/T]GAAAGTCTGCTGGGG	10391
rs766468910	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68584479	GCTGGTTGGGAGTGT[G/T]GGCGCTGGCTGGGCC	10391
rs766473650	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68683141	GCTCCTGACCTTGAC[A/G]GAGCTCCACCCGCCC	10391
rs766501902	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68715121	CTGCCCATGAGGCAC[A/C]GGGGAGAGCTGTCTT	10391
rs766560423	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68692148	ATCCCGGCTTTGCTT[G/T]CAGCTGCTTGACCTT	10391
rs766612780	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68673412	GAGTCCGGCTACTTG[A/G]GAGGCTGAGGTAGGA	10391
rs766661275	in-del	-/TGGA			intron-variant	CORO2B	GRCh38.p7	15:68697194	GGATGGATTGTTGGA[-/TGGA]TGGATGGATGGATGG	10391
rs766676604	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68567804	AGGCAGGTGGATCAC[A/G]AGGTCAGGAGTTCAA	10391
rs766701433	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68626720	CATCAAGTCCATTTC[C/G]TTGGCTGGGGAGAGA	10391
rs766718142	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68637307	TGGCGAGCCCCTCGG[A/G]ACTGTAGGCTGGTTC	10391
rs766826264	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68627631	GGTGAGAGGCACTGT[A/G]ACAAATGTGGTCTTC	10391
rs766836817	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68599838	TGTCTAATTGTGCTC[A/G]AGGCCTGAGTGAATT	10391
rs766853077	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68609696	CTGCCATTCTTCTTC[C/T]AGGACATCCTGTGAC	10391
rs766863708	in-del	-/TC			intron-variant	CORO2B	GRCh38.p7	15:68642286	GGGTTGGGATTTGAA[-/TC]TAGGTGTGCGTGGCT	10391
rs766886754	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68676671	TAGCATGCGCACACC[A/G]CAGCCACCTGAGGAG	10391
rs766894596	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68655808	CTCAACAGGAGGCCA[G/T]GTAGAGACTTGCTGT	10391
rs766901386	snp	A/G	6.67724e-05	0.00577769	intron-variant	CORO2B	GRCh38.p7	15:68715355	GTGTGCTCATGGCAC[A/G]GGAGGACATCTGGCC	10391
rs766903498	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618527	CAAAGGCTGGGAGGC[A/G]TGAGTGCGCAGCTGA	10391
rs766915455	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68569970	CTTTGGCTGAGGAGT[C/T]ATTGGTCAGTGGGGT	10391
rs766938244	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68718098	ACTGCCCCTCATCCC[-/C]ATGATAGACGTTCAG	10391
rs766940072	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68619295	CTTTCCTTTAGCCTG[A/T]ATTTTATCACTTAGA	10391
rs766945333	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68692751	TGATTCTCATGGCTC[A/G]GCCTCCCAAGTAGCT	10391
rs766967711	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699301	CCATCTGAGCATCAG[C/T]GGACCCCACCGAGTG	10391
rs766969543	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68712028	TTACCCAGGTCCACC[A/G]CAGGCACAGGAGGAG	10391
rs766993226	snp	A/G	6.62866e-05	0.00575664	intron-variant	CORO2B	GRCh38.p7	15:68695264	ACACGTCGGTGAGCA[A/G]AGGGGTGCTCCCGGA	10391
rs766995770	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68599824	TCAAAAATTAATCTT[C/G]TCTAATTGTGCTCGA	10391
rs766995941	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68606303	GTGGTGGGGCTTAGC[C/T]AAGCAAGCATATTAG	10391
rs766999387	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68645611	TTGGACAAGCCACTC[C/T]CTTGGTGTACACAAG	10391
rs766999586	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68595520	CTGGGATCCCCTTCC[C/T]TCAGTTCAGCCCCTT	10391
rs767018149	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68605835	GTTCAAGCAATTCTC[C/T]TGCCTTGGCCTCCTG	10391
rs767031160	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68600809	TTCCTGGCCCTTGAG[C/T]CCCTCAGTCTGGTCC	10391
rs767037439	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68681420	CCTGATTTGGGGGCC[A/G]TATTTTCCCAAACCA	10391
rs767057797	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68711147	CTTCCATGCCCACAC[C/T]CTTTGCCTGGCCACT	10391
rs767066036	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68725240	CAGGCATGGTGGCAC[A/C]TGCCTGTAATCCCAG	10391
rs767086766	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68563183	AGCAGAGGAAAGAAA[G/T]AATAAAGATTAGAGT	10391
rs767119928	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68708625	CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	10391
rs767123237	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68573118	CGTAGAGGCCTCAGA[C/T]CAGCCTGTGTTCAGG	10391
rs767125761	snp	A/G	2.38769e-05	0.00345512	synonymous-codon	CORO2B	GRCh38.p7	15:68710734	TCTCCCTCTGCAGGT[A/G]CGGATCTGGGAGATC	10391
rs767170030	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68576254	GCACAAGGGGATGTG[C/G]CATTGTCTGAGTTTG	10391
rs767179215	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68695806	CCATTCAATGAGAAG[A/G]GAGAAGAAACAGGAG	10391
rs767217155	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68624448	ACACAAATAACAATC[A/G]TGATCAGCACCACAT	10391
rs767224667	snp	A/G			splice-donor-variant	CORO2B	GRCh38.p7	15:68719553	AGGACAGAGAATGAG[A/G]TAAGGAATGTAAGTT	10391
rs767226574	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68706519	TTTTGGCTTCAAAGA[C/T]CTTTCTTGATGGCCA	10391
rs767254676	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68666230	AACATTCTGGGTAGC[A/G]GACATAAAACCTGGC	10391
rs767277479	snp	C/T	3.32823e-05	0.00407922	intron-variant	CORO2B	GRCh38.p7	15:68725821	TGGGCCCTCCTTGGC[C/T]CCCTCTCTTCCTCCA	10391
rs767279020	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570527	ACACTGAGGCAATAT[C/T]AGAGGCTAAGATTTT	10391
rs767304899	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68634620	GGGACCAATAGCTTC[A/C]GCATCACCTGGCAAC	10391
rs767319471	snp	C/T	1.68937e-05	0.0029063	intron-variant	CORO2B	GRCh38.p7	15:68719574	AATGTAAGTTATTAC[C/T]TCCACAGGCCCTGGA	10391
rs767371780	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68641628	GGCTCAGGAGAGCCT[A/G]TCAGGTCAGCATGTC	10391
rs767384052	snp	C/T	3.39951e-05	0.00412267	intron-variant	CORO2B	GRCh38.p7	15:68714092	AGGAAGCATCGTTGC[C/T]TCGGAGGTCACTTCC	10391
rs767407404	snp	A/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614809	ACTGGAGCGCTTTGT[A/G]TCCTGACTGTGCCCC	10391
rs767414382	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68571893	GGTAAGGGCTGGGAG[C/T]TCAGTGCAGGGAATG	10391
rs767461739	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654219	TCTGCAGAAATGGAA[A/G]TGTCGCTCTCTTATT	10391
rs767469787	snp	C/T	1.65138e-05	0.00287343	intron-variant	CORO2B	GRCh38.p7	15:68714668	TGGCTGGAAAGGTAG[C/T]AGGAGGTGGGGGAGG	10391
rs767471997	snp	A/C/G	5.03473e-05	0.00501712	missense	CORO2B	GRCh38.p7	15:68645182	GGCGTCCGCAATACC[A/C/G]TAGCTCCAAGTTCCG	10391
rs767482685	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625204	ATCTCTAAACTTGAA[A/G]CTTTTCCACAGTTTA	10391
rs767517372	in-del	-/TTTTTTTTTT			intron-variant	CORO2B	GRCh38.p7	15:68723117	ATGATACATACATTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTA	10391
rs767555301	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606755	AGCATAACTGAACAC[A/G]GAGTTATGTTTCCTC	10391
rs767561960	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68623240	TTGCTTAGGGTCACA[C/T]AGCGAGGAACCGGCC	10391
rs767562976	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68582022	GCAAGTGGAGAAGAG[A/G]AAAGCAGATGGCAAG	10391
rs767591914	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68611140	TCTCTATATGTACAC[A/G]CATGTTGGAGATGAT	10391
rs767595604	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68692360	AAGGCCAAAGCAGGC[A/G]GATCACCTGAGGTCA	10391
rs767596652	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68653874	GGAAAAAAAAAAAAA[-/T]GCCTGAATCTTCATC	10391
rs767603047	snp	C/G/T			intron-variant	CORO2B	GRCh38.p7	15:68725347	GCACTACAGCCTGGG[C/G/T]GACAAAGCGAGACTT	10391
rs767607754	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68604563	AATATGTGTGTGTCC[-/T]CCCCAGAGGACCACT	10391
rs767629491	snp	A/G	1.64909e-05	0.00287144	missense	CORO2B	GRCh38.p7	15:68645286	AACCACTTCTGTGCC[A/G]TCAACACCCGCTTCC	10391
rs767647191	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68693661	TCCACGCCCCTTGTT[A/C]CATCCGTTTGTGGAC	10391
rs767647645	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68622193	TTTGTAGTGGGTGCT[C/T]GGTACATTCACGACA	10391
rs767661254	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68593691	ACTCTGAAAAGAGCT[A/G]TCAGTCCAGTTTGTC	10391
rs767679962	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68643790	CACCTGTAATCCCAG[C/T]GCTTTGGGAGGCCGA	10391
rs767692509	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68568941	CACGTTTACCTATGT[A/G]ACAAACCTGCACGTT	10391
rs767736530	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68599887	CTCTGTGGGCCTGGG[A/G]TCTCCATGGCAACGA	10391
rs767737727	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68680952	GGCGCGGTGGCTCAC[A/G]CCTGTAATACCAGCA	10391
rs767743523	snp	C/T	4.33454e-05	0.00465519	synonymous-codon	CORO2B	GRCh38.p7	15:68710872	GTTCAGCGCTGGCTA[C/T]GACTACAAGGTATGC	10391
rs767770613	in-del	-/CCTC			intron-variant	CORO2B	GRCh38.p7	15:68683716	GACACACCTGCCTCA[-/CCTC]CCTCCCTGCAGAGCA	10391
rs767782629	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68567906	GCGCCTGTAATCCCA[C/G]CTACTTGGGAGCCTG	10391
rs767784211	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68600886	TGCAAACCCAGCAAT[A/T]TCCCCACAACCACAA	10391
rs767795196	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68651949	TACAAACAACAACCG[C/T]GAAGATGCTTTGCCT	10391
rs767795244	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68638332	GCTAGTGTTGAGCAA[A/G]CACCCATCCTGGGCC	10391
rs767805423	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68685957	AAATCTAAGGGGCTT[C/T]GCAACTGAGCTGCCG	10391
rs767825259	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68627918	AGAAGTTCGATGAGG[C/T]TCTGTGCTGAGGGAG	10391
rs767852090	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658022	CTGTGGGGCTCCCCA[A/G]ACTCCTAAGCTTCAC	10391
rs767855906	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68712359	TACAAGACCAGAAAG[G/T]TTTCTAGTACTATAG	10391
rs767860118	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68697019	CAGAGACCACAGCCT[A/G]TTTGGTTCTGCACCC	10391
rs767872704	in-del	AGAAGTTTTG/GAAGTTTTGAAAAGAA			intron-variant	CORO2B	GRCh38.p7	15:68605133	AAAAAAAAAAAAAAA[AGAAGTTTTG/GAAGTTTTGAAAAGAA]AAACTTCAATCTCCC	10391
rs767918120	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68668941	AAATTAGCTGGGCGT[A/G]GTGGCATGTGCCTGT	10391
rs767918871	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68646380	TCCGCCAAATCGCTC[A/G]GGGGGAGGAAGAGGT	10391
rs767946410	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68679705	GACTTCTAGGGGTTC[G/T]GAGTGCAATATGTTC	10391
rs767992340	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68589015	TCATCACAAATCTTT[A/C]TTCTAGAGACCCTGA	10391
rs768006761	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68644255	ATTGCTTTAATCATG[G/T]GCTTTGTCATCACAT	10391
rs768015375	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68617801	AACTTGAAATCCCCA[A/G]TGGGTGGTTGTCGTC	10391
rs768046937	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597954	GTTTTGGAAGTTGAT[A/G]AGTCTGTGGGGGTGG	10391
rs768097007	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68656838	GCTAGTCCTAACCCC[A/G]AGGCTGTTCTGAGGA	10391
rs768110570	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68687597	TGAAATGCACTTTCA[A/G]TTAACTATATAATTT	10391
rs768129430	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727122	TCTAGGGATGCTCTG[C/T]GTGTGTCTCAGCACC	10391
rs768134533	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68650062	ATGATACACTGTTAC[A/G]TGAAGAAATGCAATA	10391
rs768140655	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68714297	AGATTGAGAGACTTA[-/C]CTGGGGACACATAGC	10391
rs768154620	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68637952	TTTGAGATCCGAGGA[A/C]AGGATACAATTTGCT	10391
rs768164995	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68710892	ACAAGGTATGCAGTG[A/G]GCAGGCAGCTGGGTG	10391
rs768192321	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68590283	AGGAGCAGCCTGGGA[A/G]CCACAAACTCAGTGG	10391
rs768214435	snp	C/T	1.64988e-05	0.00287213	intron-variant	CORO2B	GRCh38.p7	15:68719139	TTCTGCTCCTCCCAC[C/T]GTAGTCAGATTCCTA	10391
rs768222598	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68648658	CCGTCTCAAAAAAAA[C/G]AAAGAGAGAGAAAGA	10391
rs768224634	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68661443	TTTCAGGGACAAAAC[A/G]TTCAACCAATCCAGA	10391
rs768231284	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566392	CTGGCTGGTTCTAAA[A/G]CCTTATCTTCCCGAT	10391
rs768242495	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68610566	CCTTCCATCACAAAG[C/G]CCCTCCTCCAGCATC	10391
rs768273711	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648902	GACCTAGCAATTCCA[C/T]TCTAGGAATTCATCC	10391
rs768280068	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68581123	AAGCAGGGATGGGAC[A/G]GGGAGTCCATGAAAG	10391
rs768320498	snp	G/T	1.65097e-05	0.00287308	missense	CORO2B	GRCh38.p7	15:68711612	CGGATGTGATCCTCT[G/T]CATGTCCTTCAACAC	10391
rs768340473	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68627398	CAAGTGCAGGTGGGT[A/C]CCCAGGAAGAAAGAG	10391
rs768369110	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600229	TGCTGTTGTTTTGCA[A/G]ATCTTTCTAAAATGT	10391
rs768389421	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68666228	GGAACATTCTGGGTA[A/G]CGGACATAAAACCTG	10391
rs768411106	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68667736	GCACTGAAGATGGGC[A/G]GGGGGATGTGGAGGA	10391
rs768414269	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68657376	AAAAAAATTAGCCAG[G/T]TGTGGTGGCATATGC	10391
rs768425570	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68567078	ACCTATAGCACAGAG[A/T]TACTGTAAGAATTAA	10391
rs768429506	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68680312	TTTCATTCATGTCTC[A/C]CACTCTGCTGGAAAC	10391
rs768448128	in-del	-/GATG			intron-variant	CORO2B	GRCh38.p7	15:68633804	CTCTTCCATGCCATC[-/GATG]CCCTGGCTGTAATGT	10391
rs768461233	snp	A/C			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727287	TGAGGAAACCGAGAG[A/C]AGTGGCCCAAGGTCA	10391
rs768474305	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68713062	CTGCCAACTTACCTG[A/G]TGCCGAGGACTGTTG	10391
rs768483040	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68694018	TTTTTGTATTTTTAG[A/T]AGAGATGGGGTTTCT	10391
rs768485166	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68628676	GGAGGCACCATTATT[A/G]TCACCACAGTTGATG	10391
rs768533418	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68557597	CCAGCTTCACAAAGG[C/G]AAGGGCAGCATCCTA	10391
rs768559948	snp	A/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616471	CCACCAAGGTCTCTT[A/G]CTGCCCGGCCTGCTG	10391
rs768573316	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68643929	GTAATCCCAGCTACT[C/T]AGGAGGCTGAGGTGG	10391
rs768615249	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68668479	AGAGACTTGTGATGG[A/G]TATGTTAGGTAAGAC	10391
rs768630705	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68635184	CACTCCTCTCCCCAC[C/T]GGTCTTGAACCACCC	10391
rs768646302	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68589466	GACAAAATCTCTACT[C/G]TTAGAGATCTGTGGA	10391
rs768661354	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68664049	CAGCTGGAACTCTCA[C/T]ACTACACTGCTGGGA	10391
rs768675593	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726669	TGTGAGCCAGGCAGG[A/G]TAGGGATTAGTGTCC	10391
rs768694925	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68717069	AGCAGTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	10391
rs768715876	in-del	-/CCGAGCT			intron-variant	CORO2B	GRCh38.p7	15:68701068	GCACACCCCCACCTC[-/CCGAGCT]CCGAGCTCCGGAACC	10391
rs768717876	in-del	-/TTGATATA			intron-variant	CORO2B	GRCh38.p7	15:68649227	ACATATCAGGTGTAT[-/TTGATATA]TTGATATATATCTTT	10391
rs768723548	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68596853	GCAGAGCACTCCCCA[C/T]GCCCCTTCCCACAGG	10391
rs768756020	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68617332	GCTCACACCACTTTT[C/T]ACTCTTCTGTGTTTT	10391
rs768784064	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68691745	AGGGCTCTGGCCACT[C/G]CTTCTTCTAAATAGG	10391
rs768784224	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68653012	TGACACCCCATGTGT[A/C]CATCTCTTTTGGAAG	10391
rs768788800	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68597970	AGTCTGTGGGGGTGG[G/T]TATGAGTTAGAAGTC	10391
rs768798851	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68584240	TCTTTCCTTCCTTAC[C/T]GTCTCTCCCTCTAGG	10391
rs768811481	snp	C/G/T			intron-variant	CORO2B	GRCh38.p7	15:68707161	TGCTAGGATTACAGA[C/G/T]GTGAGCTACCACGCC	10391
rs768826961	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68570298	GGCTCTGCATATAGA[A/G]TACTTGCATGTAAAC	10391
rs768848903	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68638508	GCCAAGATAGAAACC[A/C]CTGGATTCTTTCTGA	10391
rs768855141	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68654052	GAATGTACAGTAAGT[C/G]ACTTTGGAAAAGGGA	10391
rs768889026	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68596492	GAGCCTGCCTGCCAC[A/G]GAAAGCACAGTGAGC	10391
rs768906081	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68613431	ACCTGACTTCTTCCC[C/T]ATTTCAACCCTCTCA	10391
rs768936797	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68588178	GTATTTCAAGGCCCT[C/G]AGATTTAGGCAGTTC	10391
rs768938752	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68714792	TGGGCCTCACCTTTC[C/G]CATCCACACCTGCCC	10391
rs768942910	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68665690	TGTTACACGTATTTA[C/T]CTTTTTTATTGTATT	10391
rs768961821	snp	A/G	1.66604e-05	0.00288616	intron-variant	CORO2B	GRCh38.p7	15:68725793	GGAAATCCTTGTCTC[A/G]CCTGCTCTCTCCTGG	10391
rs769006765	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68620333	TAAATGTTAGAAAGA[A/G]CCAATTTAAAGAAAA	10391
rs769011769	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68695485	GTGTGATTGAGCTTG[A/G]AGGTGTTGCTTTTGT	10391
rs769011790	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68707938	ACATCACTCCCTCCC[C/T]CAATTCCCCCCCTCC	10391
rs769029859	snp	A/G	1.65173e-05	0.00287374	missense	CORO2B	GRCh38.p7	15:68719506	AGAGTGTTGTGGTCA[A/G]CGGAATAGATTTATT	10391
rs769034586	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68602360	TGGGAGACAGGAAGG[A/G]TTTTGCCATGATTGA	10391
rs769034707	snp	C/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614555	ATTTTAAAGAAAAGA[C/T]ATGGGGACTAAGACA	10391
rs769058492	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68585453	GGGGTAGATTCTATT[A/T]TCCATCCCATTTTCT	10391
rs769097821	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68660254	TTTGTTTGCTGGTGC[G/T]GCTTCTTCTATGTCT	10391
rs769099219	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702448	GCCCCTCCTACCTCC[C/T]TGGGTTTGGTGGGAT	10391
rs769115745	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68651566	ATCACTTGGAGCGTT[A/C]GTTATAAGCTATTAA	10391
rs769120088	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630873	ACATCCTCAAATGGA[A/G]GCAAAGGCGGGAAGC	10391
rs769176049	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68593204	ATCTCTTAATACTGT[C/T]ACATTGGCAATTAAA	10391
rs769189564	snp	A/T	1.68021e-05	0.0028984	intron-variant	CORO2B	GRCh38.p7	15:68713876	TCATGCCACTGCAGA[A/T]CCCACATGTTGGGGA	10391
rs769199752	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641491	AGAAGGAGCAGGGAA[A/G]AGGAGAAGGGGGAGG	10391
rs769199973	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68682580	CTGTGCTGAGGACTG[C/T]TGGGCTCAGGCAGGA	10391
rs769206052	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68715695	CCGTGACTCCCAGAT[C/T]CCAGCAGCAGCTCTG	10391
rs769222104	snp	C/T	1.66902e-05	0.00288874	intron-variant	CORO2B	GRCh38.p7	15:68714058	TCAGCCACGGGGAGG[C/T]CTGCTGGGTTTGGGC	10391
rs769251126	in-del	-/AAGAAAG/GAAAG			intron-variant	CORO2B	GRCh38.p7	15:68576173	AAAAAAAAAAAAAAA[-/AAGAAAG/GAAAG]AAAGAAAGAAAGAAA	10391
rs769259929	in-del	-/AAA			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577726	ACTACTCCGGTCTCA[-/AAA]AAAAAAAAAAAAAAA	10391
rs769268670	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68669477	GGTGGGATGTGTTCT[C/G]TGACTGAAATTGCAG	10391
rs769282468	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600562	TCTGAACTCCGTCCC[A/G]CCCCCGGACCCAGGC	10391
rs769301235	in-del	-/AC			intron-variant	CORO2B	GRCh38.p7	15:68704042	TCTACACACACATAC[-/AC]ACACACACACACACA	10391
rs769302868	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68568442	CCTTTACCCTCTGAG[A/G]GGTTGTCAGAGGGTA	10391
rs769313892	snp	A/G	1.79754e-05	0.0029979	splice-acceptor-variant	CORO2B	GRCh38.p7	15:68645158	CTCCTGGCCCCTCAC[A/G]GATGTCCTGGCGTCC	10391
rs769321957	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68559975	AACCTGTGTAAGGAC[A/G]ACTGGCGGGGAGAGC	10391
rs769325744	snp	C/T	1.67077e-05	0.00289026	intron-variant	CORO2B	GRCh38.p7	15:68711743	GATTGAAGGGGAAGG[C/T]ATTGAGGGCTGGGGC	10391
rs769334210	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68621193	TAATGAGCAATTGAG[C/T]ATCTTGGAGGTGCCA	10391
rs769345410	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694154	TTGTGTTATAATGGA[A/G]GGAAGCACAGAATGC	10391
rs769349630	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68637973	ACAATTTGCTTCCAT[A/G]TGGAGTGTACATAGT	10391
rs769366778	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682146	GGACAGCCCACAGAG[A/G]GAGAGTCCTCCAAAT	10391
rs769380979	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68601383	CCAGCATCCTCTGAG[C/T]GTTGTCAGGTGCTGT	10391
rs769399073	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68681439	TTTCCCAAACCAAGG[G/T]TTAGGACACCCATGA	10391
rs769422461	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68612005	CAAACTCCTGGGCTC[A/G]AGCCATCCACCCACC	10391
rs769432730	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68713275	TATTGTTATGGGGAT[A/G]AAAAGCAATGCCCCT	10391
rs769454367	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68712844	GGAGGAGCTAGGATT[C/T]AAACCCAGAGCCCAT	10391
rs769493658	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68617487	CCCATACTGGACCTC[C/T]ACATTCCCACCTATA	10391
rs769509614	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68589683	CTAGTAGTTGCCCGA[C/T]GTTGGCAGGCCAAGG	10391
rs769514483	in-del	-/CT			intron-variant	CORO2B	GRCh38.p7	15:68558861	GCCAAGTTACTTCCC[-/CT]CTCTGGCCTCAGTTC	10391
rs769544043	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68588529	AGGCGAGGGAAGGTG[C/G]GTCCCAGAGCACAGT	10391
rs769579028	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68700292	CCACAGGGGCCCAGA[A/G]GGAAGCTCTTCACAG	10391
rs769582849	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68625105	CACTCGGCTGTTCCT[C/G]AGCCTCCTTGCAATG	10391
rs769586807	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727354	ACACATTTTCTTTTA[C/T]TCCTTCTTTTTTCCT	10391
rs769627800	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68678923	AGAGGCCAGGGGACC[A/G]CTGTACTCAGGGTGT	10391
rs769633186	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601785	AGGGCCCAGGCCTGG[A/G]AGGGCTATTGTCTTA	10391
rs769643272	snp	A/G	2.88855e-05	0.00380025	intron-variant	CORO2B	GRCh38.p7	15:68710705	TGGCCGTGTCCACCC[A/G]GCCTGGACCCTCATC	10391
rs769661720	snp	A/G			downstream-variant-500B	CORO2B	GRCh38.p7	15:68728175	TTCTACCGCTATTCA[A/G]TAGATGCTGCCCCGT	10391
rs769668998	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68599323	CCAGAGGGCAAGCCC[C/G]ATGCCCTGAGTGGGA	10391
rs769688476	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68645054	GACCCAGGGCCTGCT[C/T]ACCTGCTGCACCTCT	10391
rs769691947	in-del	-/TATG			intron-variant	CORO2B	GRCh38.p7	15:68649657	GAAGGAATTTTAAAC[-/TATG]TATTTATTAACTTGC	10391
rs769707291	in-del	-/AGA			intron-variant	CORO2B	GRCh38.p7	15:68638299	AGACTCCCTCACAGG[-/AGA]AGGAGAGAGGGTAGA	10391
rs769723093	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68634318	CCAGCTCTTTTACTC[A/G]CTCGCTGGCCGGCAG	10391
rs769747757	snp	C/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68614686	GGATTTCAGGACTCC[C/T]GGGAGCCCTCTGGGG	10391
rs769764336	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68625894	ACAGGCATGAGCCAC[A/C]ACACCCAGCCCAGCT	10391
rs769771138	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726390	CCGCCTGGAGCTCTC[A/G]GCATCACTGAAGGTA	10391
rs769773459	snp	A/C/G	3.32111e-05	0.00407488	intron-variant	CORO2B	GRCh38.p7	15:68715327	GTAAGTGGCCCCGAG[A/C/G]CTGCCACAGCTGGTG	10391
rs769791190	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577087	GATGCCTTAGGAAGG[G/T]TTTTGCACAGAGGAG	10391
rs769792822	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68599414	TTCAATTACAGGTTT[C/T]TGAATGATGTATTTA	10391
rs769793402	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68563734	TACAGAAAGAAAAAA[G/T]ATTATAAATGAATAA	10391
rs769814283	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68646460	GGAGGATGGATTTTT[C/T]CAGTCTCTCCTACCC	10391
rs769895179	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726500	CCTGCCTCACCCGAC[A/G]AGGACAGCGAGCGGC	10391
rs769928205	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68667543	TTTGAGGCCCAGGGT[A/G]CAGATGAGTCTTGGC	10391
rs769928282	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654105	AAAAGTCGCAACTTT[A/G]TTTCATTTGTCTGAG	10391
rs769930225	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68590858	GTGGAGAGGAGAGGA[C/T]AGCCAAGCTTATTCT	10391
rs769961021	in-del	-/AA			intron-variant	CORO2B	GRCh38.p7	15:68660033	GGTGGAAGGGAAGAC[-/AA]GAGAGGCAGGCAGGC	10391
rs769984709	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68617013	GAATTTTCCCAAGAA[C/G]CAGGTATATGGAGAG	10391
rs770001120	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68673666	ACATAGTGAAACCCC[C/G]TTTCTACTAAAAATA	10391
rs770014058	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68716704	AGCTCTGAAAGATGG[C/G]AAGGAGAAAGAGCAG	10391
rs770015285	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68642297	TGAATCTAGGTGTGC[A/G]TGGCTTCCAGTCCGG	10391
rs770027004	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68585624	TGGGGCATGATCGTA[C/G]TCTGCTTCCACTCCC	10391
rs770042208	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603419	GACAGAGGAGCCTTC[A/G]TGGAGGACAAACTGC	10391
rs770044613	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703056	GGTCTCGAACTCCTG[A/G]ACTCAAGTGATCCAC	10391
rs770046193	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68633142	AGTGTGGGTCACTTC[C/T]ATGGAGCAGAGCTGT	10391
rs770075646	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68593254	AGAGATATTCAAACC[A/G]TAGCCATGGGTGTAT	10391
rs770086605	snp	A/G	1.672e-05	0.00289132	intron-variant	CORO2B	GRCh38.p7	15:68714066	GGGGAGGCCTGCTGG[A/G]TTTGGGCTAAAGGAA	10391
rs770101314	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639547	CAAGGTGGTAGACCC[C/T]AAAACTCCTCTCTGT	10391
rs770150408	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68684277	CCTGTCAATATGTAC[A/G]TAGATGACCCGCAAG	10391
rs770165582	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68592601	AAATAAATGAAAAAA[G/T]ATTCTTCCCAGCTTT	10391
rs770193885	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68568387	AGACACAAGTGCTGG[C/G]TACCATTTTCATCAT	10391
rs770201446	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68632410	GTCAGCCAGACAGGA[C/T]TCTTCATTTGCTAAC	10391
rs770220541	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68684347	AAGGCTTTTGTTTAC[C/T]TGATTAATTGGCCAA	10391
rs770221254	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68661572	GGGTAGTCCTGATCA[C/T]AAACCTGACTACATT	10391
rs770244731	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68562678	ATTATAAAATACTTC[G/T]AGACAATGAAAACAG	10391
rs770264174	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68581557	CCAGTCACTTCCATC[C/G]TTGGGCCTCTGTTTT	10391
rs770264802	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68662955	TCCTAAACAGGCTAA[C/T]ACAGGACTTTTTCTT	10391
rs770273371	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68621701	AAGCTTTGGGATAAT[A/G]CAGACCTGGGTTCAA	10391
rs770275300	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722397	AGCAGTTCGGAAGCA[A/G]CCAGTTAGAAAGTGG	10391
rs770277312	in-del	-/TCTC	0.000241862	0.0109942	intron-variant	CORO2B	GRCh38.p7	15:68695112	TCAAACTAATCTCCT[-/TCTC]TCTCTCTCTCTTTCT	10391
rs770305472	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68582604	AATATCTGTTTCTAC[A/T]TTGCTATCAACTGGA	10391
rs770320165	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68674652	CGCCAGAGAAAGGCT[C/T]GTGGGCAGTGGCTTC	10391
rs770358836	in-del	-/ACACACACAC			intron-variant	CORO2B	GRCh38.p7	15:68587050	TAGGGAGATATGTAT[-/ACACACACAC]ACACACACACACACA	10391
rs770394566	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648401	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCAGAGG	10391
rs770420428	snp	C/T	3.29728e-05	0.00406021	synonymous-codon	CORO2B	GRCh38.p7	15:68645267	CACCAAGAATGTGCA[C/T]GACAACCACTTCTGT	10391
rs770421623	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658681	CATTCTTCTTTGTCC[A/G]GTAGACATCATTCCT	10391
rs770427471	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699331	GTGGTGCATGGGAGA[C/T]ACTACACGCTCCAGG	10391
rs770434054	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68559215	TTTCATTAAAAATCT[A/G]ATGTAGAAATTACCC	10391
rs770447878	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630701	TCAAACAAGAGTTGC[A/G]GAGGAAGGAGGTCCT	10391
rs770462104	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577145	ACCCAAGAGATTTAG[G/T]AAGTCCCTGGAACTC	10391
rs770467322	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68622934	GTGTCTGGTGCTTTG[C/T]ATACTTTAGGGAATC	10391
rs770472509	snp	C/T	3.95609e-05	0.00444734	intron-variant	CORO2B	GRCh38.p7	15:68645143	GCCTGACCCTTGTCT[C/T]TCCTGGCCCCTCACA	10391
rs770490718	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68688227	TTTAATAACAATTTT[A/G]TATGTTTGTTAGAAT	10391
rs770494167	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68602094	CCTCTGAAAGGATCT[G/T]CCTCGAATACTATCA	10391
rs770502025	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68590065	ACCATGAGAAGGGCC[G/T]CTGAGTTGGGAGCCT	10391
rs770510563	in-del	-/AAA			intron-variant	CORO2B	GRCh38.p7	15:68673837	GCGAGACTCCGTCTA[-/AAA]AAAAAAAAAAAAAAA	10391
rs770513859	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68669604	TTGAGCTCAATGGGC[A/G]ATGCTGGCTCTGAGT	10391
rs770517782	snp	A/G	1.67522e-05	0.0028941	missense	CORO2B	GRCh38.p7	15:68718715	GTCATGCCCAAGCAC[A/G]GGCTGGATGTGTCAG	10391
rs770529122	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68619229	GGAGCATTCAAGAGC[C/T]ATTAGCCTTTTATAT	10391
rs770536290	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640400	CTTAAAGTTTACAAG[A/G]GATACAGGAACAACT	10391
rs770583992	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601505	ATTGCGGCCATGAGC[A/G]TGCAGTGCGAGGAGG	10391
rs770644069	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606249	GTAGATAGTGTTTAA[A/G]GCCCTAAGCATGAAT	10391
rs770645724	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68719321	CTCCTTGTCTGTCCC[C/T]CTGTTTGAACTTCCC	10391
rs770706652	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68702285	ATCTGTGCAAGGACA[G/T]TCTTTAGTAGTCATA	10391
rs770724860	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68700413	CTGGTGGGATTTCAC[A/G]AGCCCTGATTTCCCC	10391
rs770755199	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68607014	GAGCCTTCTCCAAAC[A/G]TCTTGAGTCTCCCCT	10391
rs770804249	snp	A/C/G	0.000124422	0.00788651	intron-variant	CORO2B	GRCh38.p7	15:68718823	AGGGTAAGTGGGGCT[A/C/G]GGCTGGGCTCCAGGA	10391
rs770836897	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68638787	GTTGTAAATGGGATT[-/G]TAGCACCTGCCTAGT	10391
rs770908379	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68566001	GCCCCATCTTTCCTC[C/T]ACCTCTGTGGAGAGG	10391
rs770930759	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68678478	CAGGAGTTCAAGACC[A/C]GCCTGGCCAACATGG	10391
rs770986743	snp	A/G	7.82779e-05	0.00625562	synonymous-codon	CORO2B	GRCh38.p7	15:68710785	GAACATGACGGAGGC[A/G]CTCCTGGAGCTGCAC	10391
rs771028649	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68717876	GTCTGTGCTCGTCAC[A/G]GTGCCAGGCAGTTAA	10391
rs771068916	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68642604	GGCCTCCACGACTCA[C/T]CTAGGCTGCCTGGGA	10391
rs771071164	snp	C/T	1.64768e-05	0.00287021	synonymous-codon	CORO2B	GRCh38.p7	15:68714621	TGGCCTCCTGTTCCC[C/T]TTCTATGATGCTGAC	10391
rs771086232	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595999	GCCACGAGGGTGCCC[A/G]GTGAGGTTTGAGTGT	10391
rs771148118	snp	A/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616344	GCTCTCTGGTCATCC[A/T]AGTTTCTTCTCAGAA	10391
rs771151344	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68705979	CCCCCATGTGACTCT[A/G]CCTTACCCTGGCATA	10391
rs771183749	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68623815	ATGAGGTTGGAGGCG[G/T]GTGTGTTTGAGCAGC	10391
rs771205020	snp	G/T	1.64882e-05	0.00287121	missense	CORO2B	GRCh38.p7	15:68645281	ACGACAACCACTTCT[G/T]TGCCGTCAACACCCG	10391
rs771225664	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68722532	TCGCTGAATTGTAAG[A/C]TTAAAATGAGTGACT	10391
rs771231579	in-del	-/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640649	AAAAGGCATTGGGGG[-/G]AAATTTAAACACGGG	10391
rs771238627	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68693448	ATAACCTCCTAGACT[C/T]CCCTCTTTTCTGACC	10391
rs771239249	snp	A/C	0.000117315	0.00765791	intron-variant	CORO2B	GRCh38.p7	15:68645363	CCCCCTGGAGCAGGT[A/C]GGTGGCCCCTACCTT	10391
rs771245483	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68716838	TCTGTGATGTAGCAG[A/G]AGATGGGGGGAGGAT	10391
rs771281108	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68562783	AGATCGAAACCATCC[G/T]GGCTAACACGGCGAA	10391
rs771298376	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68639425	GTGGGACACCCTAAA[A/G]GGAGGTGGCTATTGC	10391
rs771320978	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68557874	ATGACAGGCATGAGA[A/G]TTGCCAGCATTACAC	10391
rs771403952	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68569608	AAAACATCTGTGTGC[C/T]GGTTTTCGTGTGGAC	10391
rs771405078	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652672	GTGTGGCCTGAGGAG[C/T]TTTTGAGGATCTAAC	10391
rs771416490	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682246	TGGAAGAGTTGCACA[A/G]GGAAAGTAATAATTA	10391
rs771419504	in-del	-/GGGGGAGGGCCC	1.65789e-05	0.0028791	intron-variant	CORO2B	GRCh38.p7	15:68714676	AAGGTAGTAGGAGGT[-/GGGGGAGGGCCC]GGGGCAGCCTGTGGG	10391
rs771491836	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68584062	CCTGTGTGAGGCATT[A/G]GGAAAACAGTGGCAT	10391
rs771529187	in-del	-/G	5.53684e-05	0.00526129	intron-variant	CORO2B	GRCh38.p7	15:68718838	GGCTGGGCTCCAGGA[-/G]GGGGGGCCTGCATCG	10391
rs771562039	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648623	CCAGTGCACTCCAGC[C/T]TGGGCCACAGAGCGA	10391
rs771580435	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727396	CCACTACGCACAAAG[A/G]GTTTATAAACACTGT	10391
rs771589491	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68663703	GATTAGTATTCATAA[A/T]ATGTGACTGGATTTA	10391
rs771597371	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68620159	TCAGATGATCCACCC[G/T]CCTTGGCCTCCCAAA	10391
rs771612448	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68658834	CTGCTCCCGCTGATC[A/G]GAATGCAACATGGAG	10391
rs771612638	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68672440	ATGTGCACCACCATG[A/C]CTGGCTAATTTTTGT	10391
rs771615435	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630805	ATTTTGGCCTTTTGG[C/T]TGTAGGCTTGTTACC	10391
rs771629544	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703605	CCTGTGAACTTCTAT[A/G]CCATATATACAGACA	10391
rs771639393	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68602244	TTTATTCCGGGGAAT[G/T]ACACTAGGTTTATGT	10391
rs771640668	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68563525	GAAAAAGAAAAAAAG[-/A]AGAGAAAAGAAAAAA	10391
rs771643596	snp	C/T	1.98049e-05	0.00314676	missense	CORO2B	GRCh38.p7	15:68710810	CTGCACGGGCACAGC[C/T]GGCGTGTGGGGCTGG	10391
rs771648289	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68603172	TGCAGAATTGTCCAC[C/T]GTGTCTTACACGCCA	10391
rs771648641	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577320	GCTCTGTCACTGTGT[A/G]CTCTTGGGCAATTCC	10391
rs771661972	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68621297	GCTAGGGGAAGCAGA[C/T]ACATAAACAGTTAGC	10391
rs771692203	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68720294	GGGATATGGAAAGCT[A/G]TGAGCATTAAAGAGA	10391
rs771742998	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68591014	GCCAGGCCCTAAGCG[G/T]CATTGAGGGTGCAGG	10391
rs771751077	snp	A/G	1.64944e-05	0.00287175	missense	CORO2B	GRCh38.p7	15:68645239	GGGAGCACTGCTTCG[A/G]TGGGATCCCCATCAC	10391
rs771781323	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68647017	AGGCTCAAACCTATC[A/G]CCGGCACCCTGCCAT	10391
rs771784266	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68599494	CAGCCATATAAGATG[C/G]ATTCGTTGGCAAATT	10391
rs771848323	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68668236	GGTCATCTGCCCCAC[A/G]ACGTGTTCACACTTG	10391
rs771855380	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68689558	TGTGTTAGTGTTGGT[G/T]TTAGTGTATTAGTGT	10391
rs771870495	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68588126	ATGGTTTATTGTGAT[A/G]TCTAATCTGTGCCCA	10391
rs771871294	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68637651	AGTGCCAGTCTTTCT[A/C]TGACAGCACATGACC	10391
rs771871889	in-del	-/CA			intron-variant	CORO2B	GRCh38.p7	15:68645847	GGCGCGATCTCGGCT[-/CA]CTGCAACCTCTGCCT	10391
rs771872216	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68598278	GGTTCCTGGCCCAGG[C/T]CATGTGGGTTTTAGG	10391
rs771874105	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68608748	CCACCCCTCCCCTGC[C/T]CAGACTCCCGAATGC	10391
rs771899522	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68698487	TTGTAAACAAGACAT[C/T]CATGGTTTGTGTCCA	10391
rs771911389	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68617073	GGGCTCTGAGGGGTC[-/A]AAAAAAATGGTCCAG	10391
rs771914673	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68579797	AGGCGCTGCCCAGTC[C/G]CGGGAGCCGCTACCA	10391
rs771954743	snp	A/G	2.71161e-05	0.00368202	intron-variant	CORO2B	GRCh38.p7	15:68710926	AGGGATTGGGGAAGA[A/G]AAAGGGGCCTTTTGG	10391
rs771959452	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640068	GGAGGAGTCTTTTCT[A/G]TTCCCTGCCTGCGCA	10391
rs771961109	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68649658	AAGGAATTTTAAACT[A/G]TGTATTTATTAACTT	10391
rs771982978	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68595082	GAGTTGTGCAGTGAA[C/G]TGGATTTAGGAAGCA	10391
rs771983841	snp	C/T	1.65789e-05	0.0028791	synonymous-codon	CORO2B	GRCh38.p7	15:68725897	CGGTTGAAAGAGGAG[C/T]TGGCCCAGAAGGACA	10391
rs771998297	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68605118	GACTCCGTCTCAAGG[-/A]AAAAAAAAAAAAAAG	10391
rs772033040	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68680195	GACAACAGTATCTTT[A/G]CAGCTGGCAGCATGT	10391
rs772042039	in-del	-/ATTC			intron-variant	CORO2B	GRCh38.p7	15:68711008	TTCATTTGCTTATTC[-/ATTC]ATTCATTCATTCATT	10391
rs772079599	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68667662	GTTTGCACTGGGCCT[C/T]TCTATTCACTACCTC	10391
rs772093490	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68676258	AGTGGCCCACACTTG[G/T]GGTGCTAACATGACT	10391
rs772187045	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68687833	AAACTCACTTTTATA[A/G]CAAACCCACTCACAA	10391
rs772188785	snp	C/G	1.64841e-05	0.00287085	intron-variant	CORO2B	GRCh38.p7	15:68715200	CTTCCTCAACTCCAT[C/G]TCTCCTGACCCCAGG	10391
rs772215225	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68606109	AAGCAGATTGGGGTG[C/G]GGAGAAGACCAGTAG	10391
rs772224881	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68621844	TCACTACAGCTTTGA[C/T]CTCCCAGGTTCAAGT	10391
rs772237673	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68599177	TTGAAAAGTCTGATT[C/G]CTGCTTTCAAAGCCC	10391
rs772239036	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68571552	AATAAACAAATATGT[G/T]ACTACCTCTTTTCTC	10391
rs772272865	snp	A/C	1.68491e-05	0.00290245	intron-variant	CORO2B	GRCh38.p7	15:68645369	GGAGCAGGTAGGTGG[A/C]CCCTACCTTCACTCC	10391
rs772275130	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68695368	CCCTTCTTCCCTCCT[C/T]TTTGTCATCTTTCCA	10391
rs772291433	snp	A/G	3.30038e-05	0.00406212	missense	CORO2B	GRCh38.p7	15:68695170	CCCAACTACCCCAAG[A/G]TCTGCGGCCACCAGG	10391
rs772304296	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68584131	GGACATGGAAAGGCC[A/G]AAGCCTTGAGTTCAG	10391
rs772335344	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694488	CTGTGGGACTCCGAA[A/G]ACTATGCTTTCAACC	10391
rs772359308	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68587838	CCACAGCCAGTCAGG[G/T]ACTCAGCCTGCCTCG	10391
rs772362269	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68573063	GTCGGGACCAAGAGG[-/C]AGCTGCTCAGGTGAG	10391
rs772362871	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68580829	ACTCAGCGCCTCCCC[G/T]GTGTCTCTTTTTGTG	10391
rs772399379	in-del	-/AGAG			intron-variant	CORO2B	GRCh38.p7	15:68648661	TCTCAAAAAAAAGAA[-/AGAG]AGAGAAAGAGAGAGA	10391
rs772407847	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68629952	ATCCAAAAGGATAGG[C/T]AATGCCCCTGCCAGA	10391
rs772475929	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68601573	GCAGCCACACAGTGT[C/T]GGGGCATCAGAAGGC	10391
rs772496226	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68612124	ATGTGTCCACACTGC[C/T]CATTGTTTATCGGAG	10391
rs772544607	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640614	TCACTGAATCCTAGG[G/T]CAGAAACTAAAATAG	10391
rs772549987	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68560720	TTGCTGGTCAGGGCC[A/G]CTCTCCAGCTGTGCT	10391
rs772555738	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671219	CTCACCACGACATAA[C/T]AGGAATTATTCTTCC	10391
rs772568286	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68559490	TTGAGTCTGGGAACG[A/G]AGAAGGGAGCGTCAG	10391
rs772572326	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68570972	TTGAATTCCTATTTT[C/T]GATGATGGCACAAAG	10391
rs772593155	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68557796	CAGTTTGCACCACGC[G/T]AACTGGGACTCCACA	10391
rs772604595	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68714249	TGCAAGATGTTCACC[C/T]TCTTTTTCCAGAGTG	10391
rs772651523	snp	G/T	3.36842e-05	0.00410378	intron-variant	CORO2B	GRCh38.p7	15:68711755	AGGTATTGAGGGCTG[G/T]GGCTCAGCTTTCAGC	10391
rs772654722	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68600630	TCAGATACCCTTGTG[A/C]CCACTATGACCATGG	10391
rs772680047	in-del	-/ATTC			intron-variant	CORO2B	GRCh38.p7	15:68711005	TCTGTTCATTTGCTT[-/ATTC]ATTCATTCATTCATT	10391
rs772691738	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68562449	ATGTTCCCAGAGTAT[A/C]GGGCTCATGTCTTTA	10391
rs772714905	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68682218	AGATAGTTATGTATG[C/T]CATGGAAGATTCTGG	10391
rs772754372	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68639265	CTCAGCTATAAGGGA[G/T]CCCTGAACCCGGCAT	10391
rs772781075	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625124	CTCCTTGCAATGGGC[A/G]GTCCGAGCATGCCGC	10391
rs772803463	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574558	GCAGAGCCTCACACC[A/G]AGAGGTCCTCATTCC	10391
rs772808749	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68715681	GAGCCTCTAGGAAGC[C/T]GTGACTCCCAGATCC	10391
rs772814724	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601387	CATCCTCTGAGCGTT[A/G]TCAGGTGCTGTGCCT	10391
rs772852902	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606209	AGGCCTAGACCAGGA[A/G]TGGGAATTTTGGAGC	10391
rs772857651	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68711052	TGAGCAACTCCTGTG[C/T]ACCCTGTCATTCCTG	10391
rs772876703	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68629024	TTGGACAGCAGAGAT[G/T]CTGTAACTTTATTTG	10391
rs772884537	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726811	GCCAGGGCCTTTCCC[A/G]CTGCATCAAGATGCC	10391
rs772891507	in-del	-/TCCTCCCCTGG			intron-variant	CORO2B	GRCh38.p7	15:68658197	GAAACTCTGTGCTTC[-/TCCTCCCCTGG]AGACAAAAACCCCAG	10391
rs772940317	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68618632	ATAGGACAGGGACTT[C/T]TTAGCATATTTGCTG	10391
rs772943252	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68723412	CAGGTGTGAGCCACG[A/G]CGCCCAGCCAATAGA	10391
rs772963178	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68700012	CCTGGGAGGGGGTGG[A/G]GCGTAAAGGAAATGG	10391
rs772970244	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68696875	CTTTTAGTCAGGCCA[A/C]AAGCATCTACCTGGT	10391
rs772970677	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68706234	ACACTGGGCATTTTT[C/T]TGCCTCCTCACCGCT	10391
rs772982116	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68563815	AACTACAAAAACTGA[C/T]GAAGAAACAGGAAAC	10391
rs773019799	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68624254	TGCAGTGGTGTGAGA[A/C]TGCAGTCCCAGCTGC	10391
rs773030980	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68724876	TGTCAATATGCTTTA[C/T]AGGAGAAATGGAGGC	10391
rs773038375	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634328	TACTCACTCGCTGGC[C/T]GGCAGGGTGGTTGTC	10391
rs773041266	in-del	-/AC			intron-variant	CORO2B	GRCh38.p7	15:68717840	ACTCATATTCACAAT[-/AC]AGGGAAAGAAATGAA	10391
rs773056418	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678982	AACTTGGCTTGACAG[C/T]AGGACCCAGTCCCTG	10391
rs773092832	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68645062	GCCTGCTCACCTGCT[A/G]CACCTCTGAGCCGCA	10391
rs773111368	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68595418	CATGACAGTGGGATA[C/T]GCCTTATCGTCAGAT	10391
rs773118340	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68605783	GCGGGAGTGCAGTGG[C/T]GCAATATCTCAGCTC	10391
rs773134210	snp	C/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68725983	CTGTTAGCTCCCCAG[C/G]TGGGCTGTTTTCTAA	10391
rs773148339	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68681129	GAGGCAGGAGAATCG[-/C]TTGAACCCAGAAGGA	10391
rs773151303	snp	C/G	1.65151e-05	0.00287355	synonymous-codon	CORO2B	GRCh38.p7	15:68719206	GCCAGCACTGACCCC[C/G]GATGAATGGCTGGGA	10391
rs773156286	snp	A/G	1.65334e-05	0.00287514	synonymous-codon	CORO2B	GRCh38.p7	15:68695238	CAACATCATTGCCTC[A/G]TGCTCGGAGGACACG	10391
rs773171347	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68674094	CGGGAGAGAGGCTGC[G/T]TGTGTGTCTCGGGTC	10391
rs773185840	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68635348	CATCTGTTGGGCCTG[C/T]GTTTTGAGCTCCACC	10391
rs773204844	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68677581	TCAGGGATTTGCTTG[A/G]AGAGGCAAAGGTTAC	10391
rs773225117	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68654957	GGCAAGTCATTTGTG[A/C]CTAAAGGGGTACAGG	10391
rs773246133	snp	C/T	2.85221e-05	0.00377627	intron-variant	CORO2B	GRCh38.p7	15:68710708	CCGTGTCCACCCAGC[C/T]TGGACCCTCATCTCC	10391
rs773276910	snp	A/G	1.6599e-05	0.00288084	synonymous-codon	CORO2B	GRCh38.p7	15:68719534	ATTAGAAAATGTCCC[A/G]CCCAGGACAGAGAAT	10391
rs773283613	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68646604	CATGCACTTGATGGC[A/G]GGAGGTCTGGGTTCT	10391
rs773291123	snp	C/G			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68641588	CACCTGGGGAACCTG[C/G]GGTAAGTGTGGACTT	10391
rs773306482	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68632418	GACAGGACTCTTCAT[C/T]TGCTAACACGGAGAG	10391
rs773310924	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68715042	TCCACCTCTCCACCC[A/G]CAGTGAGTCCCCTGT	10391
rs773347405	snp	A/G	1.67385e-05	0.00289292	intron-variant	CORO2B	GRCh38.p7	15:68714070	AGGCCTGCTGGGTTT[A/G]GGCTAAAGGAAGCAT	10391
rs773360684	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68564020	CATTCTATAAACCCA[A/G]CACTACCCTGATACG	10391
rs773397104	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68725261	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	10391
rs773412426	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68560999	AAATGGGAATTTAGG[A/G]GGGGCCATATTTCCC	10391
rs773433035	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68571757	CCTTGTTCTTGGGAA[C/G]AGGAGTTTGAAACAT	10391
rs773465289	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68719856	TTCCAGGAGTTATAA[A/G]TTCCTGACTAACAGG	10391
rs773474095	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68652024	CTCTCAGCAGGTGGG[-/T]TACAGCCATCCCCAC	10391
rs773511715	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68603437	GAGGACAAACTGCAG[C/T]AACAGTGCGAGGTCA	10391
rs773544865	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68581700	CTCTTTGTTCTCTGA[A/G]GGGTGGTCTGTTTAC	10391
rs773554995	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68704745	GGGTATGTTCTGTTG[A/G]GTTGAACATCACTGA	10391
rs773567356	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703968	CAAGGCAGAGGTGGG[C/T]AGATCACTTGAGCTC	10391
rs773581138	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68661580	CTGATCATAAACCTG[A/G]CTACATTTGCACAAA	10391
rs773608578	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68629598	TGCTGGGGATGAAAC[A/G]ATGTGCAGGGAAAGG	10391
rs773615801	snp	A/G	1.64779e-05	0.00287031	missense	CORO2B	GRCh38.p7	15:68714598	GAAGAGGAAATTGAT[A/G]GGCTCTCTGGCCTCC	10391
rs773632149	snp	A/G	1.64863e-05	0.00287104	missense	CORO2B	GRCh38.p7	15:68645268	ACCAAGAATGTGCAC[A/G]ACAACCACTTCTGTG	10391
rs773632359	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68593389	CTCCTTCCCCCAGAA[C/T]AATAGAATCAGAATC	10391
rs773641953	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68581764	GTGAGAGGTAGGATC[A/G]CTGCTGACACACTGG	10391
rs773643208	in-del	-/TGGGCTCAGGCCCCTCC	1.66032e-05	0.0028812	intron-variant	CORO2B	GRCh38.p7	15:68695286	GCTCCCGGAGGAGGG[-/TGGGCTCAGGCCCCTCC]CTGCTTCCTTTGGAG	10391
rs773645703	snp	A/C/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640853	AGGGCTGGGGTAGAG[A/C/G]AGGAGGAGCAACTGG	10391
rs773662480	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68633143	GTGTGGGTCACTTCT[A/T]TGGAGCAGAGCTGTG	10391
rs773687586	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68664527	TGGCAGGCACCTGTA[C/G]TTCCAGCTACTTGGG	10391
rs773693089	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68657851	CTACCCAGACTCACA[A/G]ACCTCCTAACAGGGT	10391
rs773698268	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604315	TGGTTCCATTCTTCA[C/T]GGTCAGCCCCCACCC	10391
rs773702172	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68638055	AGGGCCATTCAGCTG[A/C]AAAATGAATACTTTT	10391
rs773715582	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68576022	GTCAGGTGGGGTGGC[A/G]GGCACCTGTAGTCCC	10391
rs773725002	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68631429	AGCTCCAAAAAGTTA[A/G]TGAACTTGTCCAGTA	10391
rs773729936	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68567687	ATTTGGCGTATTTTC[A/G]GAAGGCATGCCCTTC	10391
rs773752963	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68693155	CTTTCTCTGCCTCAT[G/T]CTGCATCTTCCATAC	10391
rs773787615	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68622963	TCTAATCTTCATGTC[A/G]GCCCTAGGAGGTAAA	10391
rs773810434	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671048	ATTATAAAGCACTTA[C/T]GGATCCAAAAGTAGG	10391
rs773839036	snp	A/G			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727493	CATTAGCTAGGATCT[A/G]CTAGATGCATTATAC	10391
rs773888331	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68617703	CTCATTTTATAGAAG[A/G]TGAAAGTGGAGTCTT	10391
rs773926792	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68606278	ATGACCTCAGGCAAA[A/G]GGAGTTAGGGTGGTG	10391
rs773948547	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68678635	GCTGAGATTGTGCCA[C/G]TGTACTCCAGCCTGG	10391
rs773983178	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68598214	CCTGGAGAAGAGGGC[A/G]GGCAGTCTGGCTGGA	10391
rs774009907	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68707314	GTCTCAGACTCTGTG[G/T]GTTAAAAACTAGGAC	10391
rs774017522	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577172	ACTCCCCTGGGGAAC[G/T]AATAGCTGCCTACCT	10391
rs774033048	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68679260	TTTGGTGAGCTGGGT[A/G]GAGATTCAACATATA	10391
rs774038795	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68689416	AAAATCTTGACTCCA[C/T]AGAAGCTCACTAAAT	10391
rs774045900	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68646956	CACTCAGCTCCATCC[A/C]TCCAGGCCTGCAGGT	10391
rs774089074	snp	C/G	1.67329e-05	0.00289243	synonymous-codon	CORO2B	GRCh38.p7	15:68718717	CATGCCCAAGCACGG[C/G]CTGGATGTGTCAGCC	10391
rs774091525	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68613809	GTATAGATGGCTGAA[A/T]CTCCTGAAAGTCTTA	10391
rs774132477	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68562104	GTTGTCCTCCAGCCA[-/C]CCCTTCCCATGCCTC	10391
rs774166693	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68584545	CCACTTCTCTCCCAG[G/T]CCAGCTAGCTGAAGC	10391
rs774185988	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68607065	AAGCTCGAGATAGAT[A/T]TTGGGCTTTTGAAGT	10391
rs774196037	in-del	-/TTT			intron-variant	CORO2B	GRCh38.p7	15:68709461	ATTTTTTTTTCGTGT[-/TTT]TTTTTTTTTTTTTTT	10391
rs774274841	snp	C/T	5.24508e-05	0.0051208	intron-variant	CORO2B	GRCh38.p7	15:68710721	GCCTGGACCCTCATC[C/T]CCCTCTGCAGGTGCG	10391
rs774276768	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68701061	TGCCTCCTGCACACC[C/T]CCACCTCCCGAGCTC	10391
rs774318696	snp	C/T	1.66466e-05	0.00288496	intron-variant	CORO2B	GRCh38.p7	15:68725814	TCTCTCCTGGGCCCT[C/T]CTTGGCCCCCTCTCT	10391
rs774329263	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68666119	AGCAGTGAACACCAC[C/G]TAGATTAATGGTATT	10391
rs774332337	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68635547	GCTTGCAGTGTGGAC[C/T]GGTCATCCAGAGACA	10391
rs774333175	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68691828	GTGTATCGCCCGTGG[A/G]CTGCTGGCTAGAAGC	10391
rs774338650	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68722610	AGTGGACCAAAAAAC[A/C]ATGCAAAGAAATTTT	10391
rs774368043	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68643877	ATCTGTCTCTACTAA[A/C]AATGCAAAAATTAGC	10391
rs774377456	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68568642	TACAACTTCTTTTTA[C/T]AGGCATTAGCTCATT	10391
rs774397092	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68708116	GAAACTGAGAATGGT[A/G]CACCCAAGGGTGACC	10391
rs774405334	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68671745	GTTCTCACTCATGGC[A/C]GCTGGCCTCCTCTGA	10391
rs774406523	snp	A/G	9.94942e-05	0.00705246	missense	CORO2B	GRCh38.p7	15:68725883	AGGATGAGATTCGAC[A/G]GTTGAAAGAGGAGCT	10391
rs774415098	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68655515	CCTGATCCCAAAAAG[G/T]AGAAGTGTCTTATCC	10391
rs774422088	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68626047	TTCTAGCTTTCATCC[A/G]GAAATGCTGTCTAGC	10391
rs774425034	snp	C/G	1.64795e-05	0.00287045	synonymous-codon	CORO2B	GRCh38.p7	15:68714639	CTATGATGCTGACAC[C/G]CACATGCTCTACCTG	10391
rs774438473	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68636552	GACAGAGCTGGGTGG[C/T]GAGGAGGAATTCCAA	10391
rs774494966	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68675928	AGACAGATAATAAAG[A/T]GGATTATAGGGTATA	10391
rs774498663	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68574286	GGGGCCAGCATGTGG[G/T]CATGCCGCCTGGGGT	10391
rs774504923	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68716037	TGTGGGTCTGGTATT[A/G]TGGACAGGGCCTGAG	10391
rs774545606	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604213	ACCCCCTTCCCTTGA[C/T]GCATACTCCAGGGCT	10391
rs774599840	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703070	GGACTCAAGTGATCC[A/G]CCCGCCTCGCATCCC	10391
rs774697558	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68668611	GCCCAGGGCGGGGAG[-/C]CCCCAGGGTGGGAAG	10391
rs774698624	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68582862	CTGTGTTAAGTTAGA[C/T]GCTAGTGAGCTGAAT	10391
rs774706493	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68567819	GAGGTCAGGAGTTCA[A/C]GACTAGCCTGACCAA	10391
rs774719645	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694453	CTAAAAATCAGCAGA[A/G]CTGTAATTCAAACAC	10391
rs774720058	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640596	AACACATGAACCTAG[A/G]TTTCACTGAATCCTA	10391
rs774731484	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68693490	GTTAGCAGATGGGCC[A/G]TAACTGGAGAAACTT	10391
rs774747886	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722487	AGGGAAAAGTCCTAC[A/G]ATTGTACAACTCAGG	10391
rs774748454	in-del	-/GACCCCAT	3.84934e-05	0.00438694	intron-variant	CORO2B	GRCh38.p7	15:68718665	AGACGCAGTTTCTGG[-/GACCCCAT]GGAGCCACATGTGTG	10391
rs774754385	snp	A/G	1.67851e-05	0.00289694	intron-variant	CORO2B	GRCh38.p7	15:68645365	CCCTGGAGCAGGTAG[A/G]TGGCCCCTACCTTCA	10391
rs774802415	in-del	-/AC			intron-variant	CORO2B	GRCh38.p7	15:68661689	GCATATTTTTCCAGA[-/AC]AGGGCACTTTCGTCT	10391
rs774802429	in-del	-/ACAGAGCTGTCAGACC			intron-variant	CORO2B	GRCh38.p7	15:68704511	AGAGCCTGCATTCTA[-/ACAGAGCTGTCAGACC]ACAAAGCTTCTTGCT	10391
rs774805081	snp	G/T	1.65228e-05	0.00287422	missense	CORO2B	GRCh38.p7	15:68719217	CCCCGGATGAATGGC[G/T]GGGAGGCATCAACCG	10391
rs774815181	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68669745	TATATTTTTCTTGGA[A/G]AAATAAACCAAATAA	10391
rs774817089	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68645835	CTGAAGTTCAATGGC[A/G]CGATCTCGGCTCACT	10391
rs774827685	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68623855	TCCATTGTCGACACC[A/G]CGGATTACAGCAGCT	10391
rs774847236	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68582174	ACCCTGTGGTTTCTG[A/G]AGGACTCCTGCCCTA	10391
rs774901627	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68722608	AAGTGGACCAAAAAA[-/T]CAATGCAAAGAAATT	10391
rs774907003	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682252	AGTTGCACAAGGAAA[A/G]TAATAATTATAGAAA	10391
rs774910042	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68620294	ATGGCTTAAATTGCT[C/T]AGAATGATGTTTGTA	10391
rs774939023	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68601513	CATGAGCGTGCAGTG[C/T]GAGGAGGGCTAGGAT	10391
rs774941617	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68660199	AAGTCAAGAGCAGTC[G/T]TGAATAATTGGACCC	10391
rs774950326	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68612088	AACTTTCTACTTTCA[A/G]GAAGCATCCCTGAAC	10391
rs774960740	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68557914	TCCTGGTCATAGTCC[A/G]CACCTCCCAGGTAAT	10391
rs774964382	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68602546	TGTGTCTTTAACCGC[C/T]TCTCCCTATCGTGTA	10391
rs774964730	snp	C/T	1.79383e-05	0.0029948	intron-variant	CORO2B	GRCh38.p7	15:68711527	ACCCTGCCTCCCATG[C/T]ATCTGCCCTCGCAGG	10391
rs774992837	snp	A/G	0.000127986	0.00799854	intron-variant	CORO2B	GRCh38.p7	15:68718835	GCTGGGCTGGGCTCC[A/G]GGAGGGGGGCCTGCA	10391
rs775022332	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68635678	TTGTGTCAGGACCAC[A/G]TGGAGGAAAAGTTGG	10391
rs775028965	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68600826	CCTCAGTCTGGTCCC[C/T]CACGGGGAGACAAGA	10391
rs775054275	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68603720	CAAGAAGACGGCCGT[C/G]TGCAAACCAGGAAGA	10391
rs775107399	in-del	-/G	0.000281415	0.0118587	intron-variant	CORO2B	GRCh38.p7	15:68719244	CCGAGGTACCACAGC[-/G]GGGGGGCTCCACAGA	10391
rs775122583	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68587004	TCTTTCTTATTATCT[A/G]TATTGGGCCTTGGTC	10391
rs775123228	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68579913	CCATATTGGAGGATG[A/G]TTGTTGGGCCTTGTC	10391
rs775125355	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68565061	GTGAAAGTAACTTTT[C/T]GAAGTTACCATTAAT	10391
rs775126722	in-del	-/TT			intron-variant	CORO2B	GRCh38.p7	15:68686022	AGCTCCTACTTCTGT[-/TT]TTTTTTTTTTTTTTC	10391
rs775139732	snp	A/C			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577553	ACGGTGAAACCCCGT[A/C]TCTAATAAAAATAAA	10391
rs775152402	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68607374	CAGATATTTTACATG[A/T]TGACTTGGGGCTCCA	10391
rs775165158	snp	G/T	1.98967e-05	0.00315404	missense	CORO2B	GRCh38.p7	15:68710814	ACGGGCACAGCCGGC[G/T]TGTGGGGCTGGTCGA	10391
rs775169470	snp	C/T	1.658e-05	0.00287919	synonymous-codon	CORO2B	GRCh38.p7	15:68725902	GAAAGAGGAGCTGGC[C/T]CAGAAGGACATCCGC	10391
rs775185271	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68666422	AGGATGAAGGCCTCC[C/T]CCAGTCCCCAGTGTT	10391
rs775220692	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68603554	TGTTGAAGCCCTAAC[C/G]CCCAGTGTGTTTGGA	10391
rs775224593	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68648635	AGCCTGGGCCACAGA[A/G]CGAGACTCCGTCTCA	10391
rs775249278	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68573145	CAGGTGGCTCCCTCA[A/G]TGATCACCCCTCAGA	10391
rs775252580	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68697366	AGGTGGGTAGATGGA[A/T]GAATGAAAGATAAAC	10391
rs775256434	snp	C/T	2.10808e-05	0.00324653	synonymous-codon	CORO2B	GRCh38.p7	15:68710860	CAACAACATCCTGTT[C/T]AGCGCTGGCTACGAC	10391
rs775348775	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678762	GGCTCAGAAGAGCTG[C/T]CCACACCATGTCCCC	10391
rs775368340	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68677361	ATTGTACAGATGATA[C/T]AGATGAGGCCCAGAC	10391
rs775379583	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68642639	TGCAAACTAGTCTTC[A/G]GTCTTTCAGAAGACC	10391
rs775386157	in-del	-/GAT			intron-variant	CORO2B	GRCh38.p7	15:68595413	TCCCCATGACAGTGG[-/GAT]GATACGCCTTATCGT	10391
rs775426998	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68585891	GTAGGGCATTCAGCC[A/G]AGGGCAGAACAAAGT	10391
rs775440724	snp	G/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615208	TGCTTGGTCATTAAC[G/T]GGGTCTCTCTGACTA	10391
rs775461662	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68654452	ACTAGGACTCTGTGA[A/T]GTCAAGCCATGGGCC	10391
rs775499941	snp	C/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68616353	TCATCCTAGTTTCTT[C/T]TCAGAAAAGTATTTA	10391
rs775527964	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68611627	AATGGTCAGTTCTAC[-/A]ATTGATTGAATTAGA	10391
rs775530833	snp	C/T	1.64914e-05	0.00287149	synonymous-codon	CORO2B	GRCh38.p7	15:68645291	CTTCTGTGCCGTCAA[C/T]ACCCGCTTCCTGGCC	10391
rs775533925	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68584171	GTCCAGTGGGCATGA[A/G]CCAGGAGACCTCTTG	10391
rs775570551	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68704497	CAGCCAATAAGGTCA[C/G]AGCCTGCATTCTAAC	10391
rs775589575	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68627267	GAGGGATTCAGAAAT[C/G]ACTAAGACATCATCC	10391
rs775591523	snp	C/T			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615593	GAGCCCTTGGGGTGA[C/T]TGGTCATTAACCAGT	10391
rs775615107	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68582944	AGTACCCTGAGCAGC[A/G]CAATTGCCTGCTGCA	10391
rs775625407	snp	C/T	1.64841e-05	0.00287085	intron-variant	CORO2B	GRCh38.p7	15:68715204	CTCAACTCCATCTCT[C/T]CTGACCCCAGGGTGA	10391
rs775636194	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68663841	AATTAGCATTCTTAT[C/T]AAGACAGAAGTTGAA	10391
rs775653397	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68636325	CAGCCTTCTCCTTAC[A/G]TGTCCGGCCTTGTTC	10391
rs775653466	snp	C/T	3.30049e-05	0.00406219	synonymous-codon	CORO2B	GRCh38.p7	15:68695175	CTACCCCAAGGTCTG[C/T]GGCCACCAGGGCAAT	10391
rs775662400	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68676316	ACATAGGAGTCATGA[A/T]GAGCTGCACAAACCC	10391
rs775677511	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68571595	AACCTTCATCAATAC[A/G]TCATAATACCTCATA	10391
rs775678806	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634256	GCATGATCTTGTGCA[C/T]GACAGTCTAGAAATG	10391
rs775691797	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68596205	GCATGCACTGTGCCC[A/G]TGACCCTAGGTGATG	10391
rs775710792	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68624003	GGAGGATTTTCAGCC[A/C]TAGAGACTGGGTGAT	10391
rs775730454	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68569989	GGTCAGTGGGGTCTG[A/T]GGCCTTGGGAAAGTT	10391
rs775737687	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68568983	TCCCAGAACCTAAAA[G/T]AAAATAAAAATTTTA	10391
rs775748585	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68682473	CAGAGGCTTAGCAAG[A/G]GGCTCAGGATGTTTA	10391
rs775786747	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68668414	CAGTCGTTAAGATTA[-/C]CATCAGACAGTGATG	10391
rs775816286	snp	C/G	1.68354e-05	0.00290128	intron-variant	CORO2B	GRCh38.p7	15:68711756	GGTATTGAGGGCTGG[C/G]GCTCAGCTTTCAGCA	10391
rs775823325	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68559521	CGGGGTGGTGAGGGG[G/T]TAGCGGGGAGGGCGA	10391
rs775824592	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68652936	ACTGCCATTTGGATG[C/T]CTTAGAGGATTTCCT	10391
rs775826505	in-del	-/TA			intron-variant	CORO2B	GRCh38.p7	15:68712369	AAAGTTTTCTAGTAC[-/TA]TATAGGTTGAGCATC	10391
rs775831538	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68724986	ATTCTTGTCATAGTT[A/C]CTCATCAGTAGGGAA	10391
rs775876319	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68717779	CTGGAATTCCTTTAT[A/G]TGGAAGAGCAGGCTT	10391
rs775892559	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68613287	CCAGAATAGAAGAAC[A/G]GGAAATGAGCAATTT	10391
rs775951273	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640661	GGGGAAATTTAAACA[C/T]GGGCTGGGCATTACA	10391
rs775968484	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68699709	TTCCTGAGGCTGGAT[C/T]CCAACCTCTCCTGGA	10391
rs776010647	snp	A/G	1.65113e-05	0.00287322	missense	CORO2B	GRCh38.p7	15:68719499	GAAAAGAAGAGTGTT[A/G]TGGTCAACGGAATAG	10391
rs776019933	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591038	GTGCAGGGATGAACC[A/G]AAGCAGTCTCTGTCT	10391
rs776020065	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68625311	GAGGTATAATTTACA[A/T]GCATTAAAAAAACAT	10391
rs776045961	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671271	GTTGTTGTTTTTTTT[C/T]CCTACTTTCTTAAAA	10391
rs776060741	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68619396	AAACACACTGAAGCA[A/G]TTGGAGAGCATTTTT	10391
rs776070612	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68636755	GTGTGGAGGTTTGGA[C/T]TGATTCTTTTCTTCC	10391
rs776082264	in-del	-/AAT			intron-variant	CORO2B	GRCh38.p7	15:68562683	AAAATACTTCGAGAC[-/AAT]GAAAACAGGCCAGGC	10391
rs776106781	in-del	-/CG			intron-variant	CORO2B	GRCh38.p7	15:68666833	AATGATAAAAATACA[-/CG]GTTTTGTAGTCAGGC	10391
rs776117758	snp	A/G	1.6495e-05	0.0028718	missense	CORO2B	GRCh38.p7	15:68719165	TCCTACCAGGAAGAC[A/G]TTTACCCAATGACAC	10391
rs776119415	snp	A/G	2.02928e-05	0.00318528	missense	CORO2B	GRCh38.p7	15:68710828	CGTGTGGGGCTGGTC[A/G]AGTGGCACCCCACCA	10391
rs776132026	snp	A/C	1.64751e-05	0.00287007	intron-variant	CORO2B	GRCh38.p7	15:68711497	ACAAACACCCCAGGA[A/C]CCTAGCAGCCACTGA	10391
rs776214832	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68587494	TGTACGGCACTCTAC[A/G]CTTTTTAGGAATATC	10391
rs776231379	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68694066	GTCTCAAACTCCTGA[C/T]GTCAGGTGATCTGCC	10391
rs776269941	snp	A/G/T			intron-variant	CORO2B	GRCh38.p7	15:68637957	GATCCGAGGACAGGA[A/G/T]ACAATTTGCTTCCAT	10391
rs776274388	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68620129	GTTGGCCAGGCTGGT[C/G]TCGAACTCTTGACCT	10391
rs776282597	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726726	GTTGCAATGGGGAAA[C/T]GACTTATAAAGTCAC	10391
rs776290783	snp	C/T	1.65015e-05	0.00287237	synonymous-codon	CORO2B	GRCh38.p7	15:68711638	AACACGGACGGCAGC[C/T]TGCTCACCACCACGT	10391
rs776293210	snp	A/C/T			intron-variant	CORO2B	GRCh38.p7	15:68566404	AAAGCCTTATCTTCC[A/C/T]GATCACCACCCAAAA	10391
rs776302071	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68642689	TCACAGAGCAGTGCC[C/T]CACCCCCAGGATGGA	10391
rs776313519	snp	C/T	1.64838e-05	0.00287083	intron-variant	CORO2B	GRCh38.p7	15:68715212	CATCTCTCCTGACCC[C/T]AGGGTGATGGAAACA	10391
rs776376188	in-del	-/ACACACAC			intron-variant	CORO2B	GRCh38.p7	15:68587052	GGGAGATATGTATAC[-/ACACACAC]ACACACACACACACA	10391
rs776397385	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68699913	AGATTCATCACGCTC[A/C]ACATTTACATCACAG	10391
rs776413722	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68698874	GAGGGGCAGGGCCCA[C/T]CCCACCCACCAAAAC	10391
rs776413967	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68588477	AAACCTTGATCTGTA[G/T]TATCCCGGCTCTCTG	10391
rs776414135	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68573464	GGCAGCAGAGAGGTG[C/T]GCCTCTGCCAGGCCA	10391
rs776465536	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68617369	ACTTTTCTGTTTAAT[A/G]TATCCTTTGTCCTCC	10391
rs776475783	snp	A/G	1.743e-05	0.00295206	intron-variant	CORO2B	GRCh38.p7	15:68645400	AGCTGCAGCTCCAGG[A/G]CAGAGAGGAGCCCTC	10391
rs776512130	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68682768	AGCAGAGCTGAGATG[-/A]AAAACCCAGGTCCCC	10391
rs776527623	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68656359	CAGCCAAGACCTTGA[A/T]TTCAGTTGCTAAGCA	10391
rs776535958	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68633765	TCTAACAGAGATACT[A/G]CAACGGAGCCGGCAG	10391
rs776589026	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68687247	AGTGAGTGCCGGAAC[C/T]GGGTGTGGAAATCCT	10391
rs776639886	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68596875	TCCCACAGGCCACCC[C/T]AGCCACTCTGGCCTC	10391
rs776656312	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68605398	TCAAGATGCTCATCA[C/T]GGCATTATTTATAAC	10391
rs776666715	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68724287	CAGGACCTTTTCTTC[A/C]AGGAGGCCCTCCCTG	10391
rs776676282	in-del	-/AAAA			intron-variant	CORO2B	GRCh38.p7	15:68673836	AGCGAGACTCCGTCT[-/AAAA]AAAAAAAAAAAAAAA	10391
rs776679591	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68571067	GATTGACATCTAAAA[A/G]CCATGCCCCAGGCTG	10391
rs776693592	in-del	-/CCCAGTTCCAGAGGC			intron-variant	CORO2B	GRCh38.p7	15:68572115	CTCCAAGGCCTTCCT[-/CCCAGTTCCAGAGGC]CCCACTCTTGCTCTC	10391
rs776699933	in-del	-/CTA			intron-variant	CORO2B	GRCh38.p7	15:68670996	TGTGGAAGAATTCAG[-/CTA]CTATGTTTGCCTCAG	10391
rs776712567	snp	C/T			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68641561	ACAGAAACTGCGGGC[C/T]GCTGAGCGCTCCACC	10391
rs776714401	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68718030	GGGGCAGAGTGAGGA[C/T]TCAAACCCCGTTGGT	10391
rs776743508	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604342	ACCCCCAAACCGCCT[C/T]TCCTACCACGAGCAG	10391
rs776762543	snp	A/G	6.60153e-05	0.00574485	missense	CORO2B	GRCh38.p7	15:68695204	ATGTGCTGGATATCA[A/G]ATGGAACCCCTTCAT	10391
rs776777167	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68602556	ACCGCCTCTCCCTAT[C/T]GTGTACTATGTTAAA	10391
rs776792994	snp	C/T	1.66239e-05	0.00288299	intron-variant	CORO2B	GRCh38.p7	15:68719398	CAGTGAGAGCGTTTC[C/T]CTTGCCTTCTTTAGA	10391
rs776823851	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68624823	GAGTAGCTGGGATTA[C/T]GGGTGCCTACCACCA	10391
rs776854503	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68584303	AGGTGCTTTCTTCTG[G/T]ACTGTGCCCAGAGGC	10391
rs776854523	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694719	AGGGAGAGTAGGTAC[A/G]CCCAGCATCTGAGCG	10391
rs776857089	in-del	-/TTTTTTTTT			intron-variant	CORO2B	GRCh38.p7	15:68723118	TGATACATACATTCT[-/TTTTTTTTT]TTTTTTTTTTTTTTA	10391
rs776876320	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68560926	TAGCACCACTCTTCT[A/G]GGTTTCCCATGGCAC	10391
rs776884650	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68671394	CATATGAGCCAAAGC[C/T]TCACCCACATGGCTT	10391
rs776929358	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68591379	AGGAGAGAACCAGTT[C/G]GGTGCTGCTGGGCTG	10391
rs776974333	in-del	-/GTAC			intron-variant	CORO2B	GRCh38.p7	15:68702754	GGAGCCAATGATTGT[-/GTAC]GTACTGTATACAGCT	10391
rs776990564	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68714920	CTGCAGTGTAGTCAG[G/T]GATGAATGATGGAAT	10391
rs777002425	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68700613	GAGGGAGGGCTGGGG[A/G]CCATAACTCTCCCTG	10391
rs777132933	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68607515	CCTGCCTCAAAGTCT[C/T]TTTTGTAAAGAGCTT	10391
rs777148481	snp	C/T	1.7081e-05	0.00292237	intron-variant	CORO2B	GRCh38.p7	15:68719583	TATTACCTCCACAGG[C/T]CCTGGAAGAGCAAGA	10391
rs777152740	snp	G/T	1.67041e-05	0.00288994	intron-variant	CORO2B	GRCh38.p7	15:68714061	GCCACGGGGAGGCCT[G/T]CTGGGTTTGGGCTAA	10391
rs777154671	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68684213	GCCTGAGAGTCTAAA[A/C]ACCCCAGGAGATTAC	10391
rs777155464	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68580262	GTCTGGCGGTGGCCT[C/T]GGGCTTGGCCGTCCA	10391
rs777171602	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68575425	TCACTGCAACCTCCG[-/C]CTCCCAAGTTCAAGC	10391
rs777202691	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68695059	CCAGTTGAGAGGCCC[A/T]GAAAAAAGGTGCTCC	10391
rs777240660	snp	C/T	1.72656e-05	0.00293812	missense	CORO2B	GRCh38.p7	15:68645169	TCACAGATGTCCTGG[C/T]GTCCGCAATACCGTA	10391
rs777241485	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68689657	CCAAGTTTGGTCTCC[A/G]GTCACACCCCCTGTA	10391
rs777256701	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68670813	TAATATTGGGTGCTG[C/T]CAGGGTTATAGGGAA	10391
rs777282690	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68583919	TGCTCTGCCCACACA[C/G]CCATTATGCCTCCTC	10391
rs777288561	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68706690	GTAGCCGGTAGACAT[G/T]AGAAAAGATGCCTGG	10391
rs777289003	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68694168	AGGGAAGCACAGAAT[C/G]CTGTGAGAGCACAGA	10391
rs777302093	snp	A/G			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632319	TCTGAAGCTTGTCTG[A/G]TGTCATCCAGGAGCC	10391
rs777320728	snp	A/G	1.65007e-05	0.00287229	missense	CORO2B	GRCh38.p7	15:68719482	TTAAGGCTCCCATCA[A/G]AGAAAAGAAGAGTGT	10391
rs777335411	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68569550	CCTACTGAAGGACAT[C/T]TTAGTTGTGCCCAAG	10391
rs777336513	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68570647	TGTGAAGTACAATGA[A/T]GGCTTTGGAAGCTGT	10391
rs777344184	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68629731	CAGGAGGACTTGGAC[A/G]AGGCTGAGGCAGAAG	10391
rs777350215	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68682912	GAGAGGTGTGTGGAA[C/T]TGGGGTGTTACAGGA	10391
rs777382397	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68612814	GCTCTGCAAATCTGT[A/C]GCTTGGGAGTTCCCA	10391
rs777389719	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68652657	TTCCCCACCACAGTA[A/G]TGTGGCCTGAGGAGC	10391
rs777397036	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68624553	CTAAAACTAATATAT[A/G]ATGTATTAGTTGTGC	10391
rs777421107	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68610151	GATCTCGGGGAAATG[A/G]GCCTTATCCTCAGGG	10391
rs777430274	snp	C/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640093	TGCGCACCCATGCAT[C/G]TGACCTCACAGTGAG	10391
rs777436506	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68590783	GGTTCCTGAGAGGCA[A/G]ATGAGGCAGGAGGGA	10391
rs777482064	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68612066	AGGAGCCACTGCACC[C/T]GGCCTCAACTTTCTA	10391
rs777507346	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68628571	AAGGGACTTTACAAT[A/G]GCTACATGTATTAAG	10391
rs777528962	in-del	-/CAGC			intron-variant	CORO2B	GRCh38.p7	15:68646171	ATTTTCCCCTTTCTG[-/CAGC]CAGCTGCTTACGTGA	10391
rs777552278	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68690050	TATTAAAAATGTATT[A/G]CTTCCCAATTATTTC	10391
rs777553758	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68618637	ACAGGGACTTTTTAG[C/T]ATATTTGCTGCCGAG	10391
rs777569234	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702246	CTGGGCAAGTTTTCT[C/T]ACCTCTGTGGGCCTC	10391
rs777588973	snp	G/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630551	GGGGACAGGTCACAG[G/T]CAGTGTTCAAAGACT	10391
rs777602604	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68589453	CTGTTGCTGCTTGGA[C/T]AAAATCTCTACTGTT	10391
rs777608172	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591754	GGACCACTCCATGGT[A/G]TGGGCCTTTCCCATC	10391
rs777612181	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68626400	CTAATTTAGAACATG[C/T]TTAATCACTGTGCTG	10391
rs777617043	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68724625	TTTTAGCATCATCTT[C/T]ATCAAGATTTTCTAA	10391
rs777660885	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68698428	CAGTCCTAGCTCGGC[A/G]TCTTATTTAACCTGA	10391
rs777688765	in-del	-/CAGATGGAGGGTCAGAGCAGTGGGGC			intron-variant	CORO2B	GRCh38.p7	15:68580372	AGCCCAGAGTGGGGT[-/CAGATGGAGGGTCAGAGCAGTGGGGC]CAGATGGAGGGTCAG	10391
rs777703626	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68617037	TGGAGAGTAGTAACC[C/T]TGGTTACCAGATGAG	10391
rs777706220	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68606989	CAAAGCTGGAGGGCA[C/T]TACAAGAAGGAGCCT	10391
rs777715914	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68600028	CAGAGGGGACCTGGG[A/G]CTGGCAGAGGGAGTA	10391
rs777768711	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68557474	GGTTCAGCGGCCAGT[A/C]TATCCAAGGTCATGG	10391
rs777807073	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68682088	ACCCTGGGTAGGAGG[A/T]ACCCCTGCTTCAGCT	10391
rs777808562	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68578238	GGCACTCAGTGGTAG[C/T]GTAGACAGTCCTAGG	10391
rs777835618	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648488	TATCTCTACTAAAAA[C/T]ACAAAAACAAAATTA	10391
rs777858414	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68693285	GGCAGGAAGTGGTGG[A/G]GAAGAGGTCACAGCA	10391
rs777878637	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574654	GCCTTATTGATCAGC[A/G]AGGCAGTTATCCAGC	10391
rs777921498	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68683399	GGCGGGGGAGGAGAA[A/G]GCCAATGCTAGTGAT	10391
rs777973221	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68559124	TGGGCGTTGCCAGGA[C/G]AGCGGCCGGCACCCC	10391
rs777986441	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68717814	CCCAGAGGAGGAGAG[A/G]CAGAGCCTTAACTCA	10391
rs777993575	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726543	TGTCTCTTCCCTTCC[C/T]ACCCTCTTGTCTTCA	10391
rs778002580	snp	C/T	8.24192e-05	0.00641894	intron-variant	CORO2B	GRCh38.p7	15:68715177	GCTCTGCCCTCCCTA[C/T]CTGCCACCTTCCTCA	10391
rs778014667	snp	C/G	1.65844e-05	0.00287957	missense	CORO2B	GRCh38.p7	15:68725875	CCGGCAGCAGGATGA[C/G]ATTCGACGGTTGAAA	10391
rs778041101	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68638449	ACTGATATTCAGACA[A/G]GTTGAGTAGGTAGTC	10391
rs778046885	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68627047	GGATCCTTAGCAAGG[A/T]ACTTACCTTTTTTCT	10391
rs778065378	snp	C/G	1.64931e-05	0.00287163	intron-variant	CORO2B	GRCh38.p7	15:68710900	TGCAGTGGGCAGGCA[C/G]CTGGGTGGAGAGGGA	10391
rs778071251	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68669039	GCCAAGACCACACCA[C/G]TGCACTCCTCCATCA	10391
rs778072656	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68623777	GGCTGCTGGGTAATC[A/C]CCGTTTGTGCCACTT	10391
rs778086487	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68594893	TCAGCCTTGGTTCTA[A/C]TCTGGGCTTTGCCTC	10391
rs778091302	snp	C/T	3.31912e-05	0.00407363	synonymous-codon	CORO2B	GRCh38.p7	15:68645342	GGGCGGCTCCTTCCT[C/T]GTCATCCCCCTGGAG	10391
rs778093448	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68589145	CTTTTCAGGGTTCGG[A/G]TCCACATTAATTTCT	10391
rs778125531	in-del	-/AGTT			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615235	ACTAACCGTGACCCC[-/AGTT]AGTTAGTAATTCCCT	10391
rs778156420	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68662957	CTAAACAGGCTAACA[C/T]AGGACTTTTTCTTAA	10391
rs778162417	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68634030	GCAGGGAGCCTCGGC[A/G]GTGGCAGCTATGCCT	10391
rs778163500	in-del	-/G	1.69066e-05	0.00290741	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726011	TAAGCCGATCTCTCC[-/G]TCGTTTCTACTCATC	10391
rs778180716	in-del	-/AT			intron-variant	CORO2B	GRCh38.p7	15:68565531	TTCAAATAAAAATAA[-/AT]ATATATATATATATT	10391
rs778202393	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68707987	ATGGGAGTCTTGGAC[-/T]TTTACTAGAGGGTTG	10391
rs778205849	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68716736	CCCAGCAGGGGGAAT[G/T]GTTAGTGCAAAGCCT	10391
rs778214782	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68563242	CCTATAATCCCAGCA[C/T]TTTGGGAGGCCCAGA	10391
rs778215261	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68582615	CTACATTGCTATCAA[C/T]TGGAAAAGCAGAGGA	10391
rs778235504	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68670262	TCACTGCAACCTCCA[-/C]CCGCTGGGTTTAAGC	10391
rs778241434	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68675814	AATTTTTACTGAGCA[C/T]CTTCTCTGTACCCGG	10391
rs778287774	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68634818	CACCTGGACCACCAC[C/T]GTGTTCAACCATAGA	10391
rs778291643	snp	C/G	1.64901e-05	0.00287137	missense	CORO2B	GRCh38.p7	15:68715272	CCCTACCTGAGTTAC[C/G]TCATGGAGTTCCGCT	10391
rs778294694	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68705795	ATCTAGAAGGCTTCA[C/G]ACTTCCAAGAGCTCT	10391
rs778302489	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68574948	AGTGTCTAGAAGAGA[C/T]CAGAACTAATACTGC	10391
rs778306689	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68562702	AAAACAGGCCAGGCA[C/T]GGTGGCTCATGCCTG	10391
rs778319531	in-del	-/CACACAC/CACC			intron-variant	CORO2B	GRCh38.p7	15:68602415	GGCTGATCACACACA[-/CACACAC/CACC]CACACACACACACAC	10391
rs778327607	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68683843	AGGTCCCTCAGTGAG[A/G]AAGGAGCATTGGAGG	10391
rs778385207	snp	A/G	1.65222e-05	0.00287417	missense	CORO2B	GRCh38.p7	15:68645217	GTCTACGGGAAGGTG[A/G]CCAACCGGGAGCACT	10391
rs778385898	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68718475	CAATTCTAAAGCACG[C/T]ACTGTGGTGAGGCAG	10391
rs778418806	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68560539	CCTGGCCTCAAGTGA[A/T]CTTCCTGCCTCCGTT	10391
rs778418903	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68663567	CAATAGCTATAAAAC[A/C]ATCAATAAATTGAAC	10391
rs778437416	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68676898	ACATCAGCCTCCCCA[A/G]GTAGCTGGGACCAGA	10391
rs778466755	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68620132	GGCCAGGCTGGTCTC[A/G]AACTCTTGACCTCAG	10391
rs778474469	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68607803	AGCCTGGGTGACAGA[A/G]TGAGACCCTATCTCA	10391
rs778475143	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68715467	AGCTGGCCCTGCTGC[A/C]GCTGTCACTGCCCAC	10391
rs778507319	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68673718	GGCATGCGCCTGTAA[A/T]CCCAGCTACTCAGGA	10391
rs778537194	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68641225	ATCCCCGGGGAACAC[A/G]CTGAGTGGGAGAACA	10391
rs778547724	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68603062	GATGGGTCTGTCAAC[A/G]GTCTGTTAGGATAGG	10391
rs778553728	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68614178	GGAGAACCTGTGAAC[A/G]CATCTTAATGTGTTA	10391
rs778554075	snp	A/G	1.66147e-05	0.0028822	splice-acceptor-variant	CORO2B	GRCh38.p7	15:68725841	CTCTTCCTCCACCCC[A/G]GCTCCTTCGAATGTT	10391
rs778565362	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566138	GGATCCTTTCTAAGC[A/G]CTTTTCATGTATTTT	10391
rs778572676	snp	C/T	0.000115631	0.00760276	intron-variant	CORO2B	GRCh38.p7	15:68714548	GGCTGAGACCAGCTC[C/T]TCTCCCTCAGGAGGA	10391
rs778589336	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68628836	GAGGCTAAGCATTGC[C/T]GGGTACAAGAGGCTT	10391
rs778615385	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654601	CCCCTTAGCTGTGAA[A/G]CCCTAGGCATCTAAC	10391
rs778624634	in-del	-/TAAAT			intron-variant	CORO2B	GRCh38.p7	15:68665545	ATTATGTTAAATTGA[-/TAAAT]TAAATTAAAGAGAAT	10391
rs778629834	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68602119	CTATCACATTGGCAC[C/T]GTCTGAGTTCTGGTG	10391
rs778646467	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68622520	CTGTGCTAAGTGACC[A/T]CCAGTTTCTTTAATT	10391
rs778647549	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630744	TGGCTCCACAGTGCC[A/G]TCAAGGACCCAGGCC	10391
rs778672659	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68591801	TGGTTCGATCTAAGG[A/G]TTGAGAACATAGGAG	10391
rs778686435	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597075	TGAGCAGAAGCATAT[A/G]TATCTTTTTTTTTTT	10391
rs778693392	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68662139	GCAGAAGCTGCTTTT[-/C]CTGTTATCACGACAT	10391
rs778732966	in-del	-/C	1.64912e-05	0.00287147			GRCh38.p7	15:68645293	TCTGTGCCGTCAACA[-/C]CCGCTTCCTGGCCAT	10391
rs778738360	snp	C/G					GRCh38.p7	15:68621210	TCTTGGAGGTGCCAG[C/G]ACCTGTGCTCATGGC	10391
rs778762121	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68581031	CAGTGATCTTTGCAC[A/T]GCTCTGCATCGTTGG	10391
rs778772455	snp	C/T	3.30066e-05	0.00406229	intron-variant	CORO2B	GRCh38.p7	15:68719126	CATGTGTCCTCTCTT[C/T]TGCTCCTCCCACTGT	10391
rs778777529	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68591636	GAGGCGGGGAAGGGG[A/T]TTCTGAGCCCCTAGC	10391
rs778786792	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68690139	TCTATAATAGTGTGC[C/T]GAGAGCCTCTTCTAT	10391
rs778792242	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68687028	TTCTGGCATTGCCAT[C/T]TCACATCTTTCTCAT	10391
rs778810342	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68657306	AGGATTGCTTGAGTG[C/T]AGGAGCTTGGGACCA	10391
rs778824853	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68605364	GAAATAATCCAAAGG[C/T]GGGGAAAAACTCTAT	10391
rs778824885	snp	A/C	1.65685e-05	0.00287819	missense	CORO2B	GRCh38.p7	15:68711561	TCATCTGGAACCTGG[A/C]TGTGGGTGAGCCGGT	10391
rs778853434	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574990	TACCCCACAATGTGT[A/G]CCGTATCCCCTCAGG	10391
rs778858229	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68599457	GGATATAAGAATCTA[A/T]TCTGTGCATGCGTCA	10391
rs778878540	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68667621	GCGTGAGGAGTGGGA[C/T]GGGTGAGGCCCTGTG	10391
rs778918933	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68629531	TTGGTACTCAGGCAA[A/C]CAAAGCTTTGACTTT	10391
rs778919163	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68649526	GCTGTAGAGCAGTCT[C/T]GTTCTCCAGCGTTCA	10391
rs778942469	snp	G/T	2.51962e-05	0.00354929	intron-variant	CORO2B	GRCh38.p7	15:68710917	TGGGTGGAGAGGGAT[G/T]GGGGAAGAGAAAGGG	10391
rs778954380	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68566911	TTTGCCTTACAGCAG[C/T]TCAAGCACCTGAGCT	10391
rs778966324	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68680019	CAGGGCTGAGTCTCT[A/G]TGGTGTCTGGGCAGG	10391
rs778975390	snp	A/C	3.34678e-05	0.00409057	utr-variant-3-prime	CORO2B	GRCh38.p7	15:68725980	GAACTGTTAGCTCCC[A/C]AGCTGGGCTGTTTTC	10391
rs779032247	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68642214	CTATCCTCTTTAATA[C/T]GGGAGTAGATGGAAG	10391
rs779053428	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68657652	CTCTAATTTCAAAGT[C/G]ATGATGTGCATACAT	10391
rs779057228	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68680305	ACTGAGGTTTCATTC[A/T]TGTCTCACACTCTGC	10391
rs779084250	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68725730	CAAGCAGTGGGAGGC[C/G]TGGGGGAATGTGAGG	10391
rs779096181	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68645993	TGGTCAGGCTGGTCT[C/G]GAAATCCTGACCTCA	10391
rs779100492	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68634169	GTAGGACCTGCTGTG[A/G]ACAGAGAATAGGGCT	10391
rs779105959	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618082	AGACTTTTTTGCTAT[A/G]GTTGCTAGTGAGAAA	10391
rs779114343	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68644803	CAGTTCCAGATACTC[A/G]GGAGGGAGTCTGTAT	10391
rs779143643	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68658950	ACGCCTTTGCCCCGG[C/T]TGTTTCTCCCTCTGG	10391
rs779174114	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68677079	GTGCCCAGTCCAAGA[A/C]CTGTTTTTGCAGCAC	10391
rs779207743	snp	C/T	0.000165041	0.00908258	synonymous-codon	CORO2B	GRCh38.p7	15:68695163	GATTGAACCCAACTA[C/T]CCCAAGGTCTGCGGC	10391
rs779227325	snp	A/C	3.29853e-05	0.00406098	synonymous-codon	CORO2B	GRCh38.p7	15:68715295	GTTCCGCTCCCCAGC[A/C]CCGCAGAAAGGCCTA	10391
rs779228239	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68613063	TCCTGATGGCCCTTC[A/G]GAGAAACCTGCTGCT	10391
rs779231661	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68584080	AAAACAGTGGCATTA[A/G]CCACAGTCCCTGGGA	10391
rs779245182	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68576744	AATGCTGGACAGCTC[A/G]CTGGTGGGAAATGCT	10391
rs779261825	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68687790	TGGCAGAAGGTGGAG[A/G]GCAAGAGAGATAGAG	10391
rs779290917	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68634904	GGTAATGCCAGTGCT[A/G]TTGGTCCACAGGCAG	10391
rs779343515	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68595884	TGAGACGGAGCGGGC[A/G]TCTGGGAGGAGGAGG	10391
rs779356954	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68695315	TCCCTGCTTCCTTTG[A/G]AGGCCTCTCTTCCTA	10391
rs779416044	snp	C/T	1.66045e-05	0.00288132	intron-variant	CORO2B	GRCh38.p7	15:68695286	GCTCCCGGAGGAGGG[C/T]GGGCTCAGGCCCCTC	10391
rs779508640	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68630485	GCTCTGTGGTCTCTG[A/G]GCCTCCTTAAAATAG	10391
rs779526154	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68669073	GAAAGAGAGAAAGAG[-/AG]AGAGAGAGAGAGAGA	10391
rs779536626	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68670092	AAAATAAAGAAAAAT[G/T]TAAAAATTTTTGAAA	10391
rs779539957	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726356	CTGTGAAGGGGGCTG[C/T]CAGGACATCTCAGCA	10391
rs779564418	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68561476	CCCCTTCCAGCTAAC[G/T]GGGGCCCAGCGGGAC	10391
rs779569660	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68649799	GCAAATCTCTTTAAT[A/G]TATGTCTGGCTTATT	10391
rs779577169	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68664876	GGTCTTTGATTAATT[C/T]CTTATTGATGGAAGA	10391
rs779579200	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68652858	CTCTCCCAGTCATGT[A/G]CCTGCCCACCTTACA	10391
rs779618213	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68715551	CCAGCATGTGCTCTG[C/T]GTCTGCACTCCTGAT	10391
rs779681073	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68662668	GAGCTTCCTGCAATA[A/G]CAACAAGAGCAGGCT	10391
rs779692073	snp	A/T	1.64944e-05	0.00287175	missense	CORO2B	GRCh38.p7	15:68645240	GGAGCACTGCTTCGA[A/T]GGGATCCCCATCACC	10391
rs779692224	snp	A/C	1.66382e-05	0.00288424	intron-variant	CORO2B	GRCh38.p7	15:68714713	GTGGGAGAGCCCTAC[A/C]CTCAATGCACCCCTG	10391
rs779697800	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68661384	ATGGGGTTCTGGGTG[A/G]CCAGAGATATTGTCC	10391
rs779759655	snp	G/T			intron-variant, utr-variant-5-prime	CORO2B	GRCh38.p7	15:68632153	CTCTGGGATGGTGAT[G/T]TGAGTGCCTCCTGCA	10391
rs779783122	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68610319	CACTCCCTGCCCTGA[A/G]GTGCTGCACTTGCCT	10391
rs779793574	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68580848	TCTCTTTTTGTGCGC[A/G]AGCTCATGCAGCCTT	10391
rs779797440	snp	C/T			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68639830	TATGTCCCAGTCTTG[C/T]GCCTTGTGCTCATTG	10391
rs779804118	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68600154	AAGATTTCTTCAACA[A/C]ACAAACAAGCCTCCA	10391
rs779807436	snp	C/T	1.6516e-05	0.00287362	synonymous-codon	CORO2B	GRCh38.p7	15:68711679	GAAGCTGCGTGTGAT[C/T]GAGCCCCGCTCTGGC	10391
rs779809824	in-del	-/CTT			intron-variant	CORO2B	GRCh38.p7	15:68691746	GGGCTCTGGCCACTC[-/CTT]CTTCTAAATAGGCTC	10391
rs779821388	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68685101	GGGTTCAGCATGATC[C/T]ACTGCCCTCGGTACT	10391
rs779880741	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68611542	TTTTTTTATCTCTGT[G/T]TGGATATATCTTCAA	10391
rs779890505	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68581201	CCAGTAACTATTCAA[C/T]ACTCCTCCACCCCCA	10391
rs779907122	snp	C/T	6.6072e-05	0.00574732	missense	CORO2B	GRCh38.p7	15:68711597	TGATTGACTGCCACA[C/T]GGATGTGATCCTCTG	10391
rs779915305	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68665789	TTAATATTTTGCCAT[A/G]TTACTAAATTCACAA	10391
rs779926882	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68568362	GTATAGAGTGCCTAA[C/T]ACAGTGCCTAGACAC	10391
rs779927135	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68693921	GCTCACCGCAACCTC[C/T]GCCTCCTGGGTTCAA	10391
rs779999896	snp	A/G	1.65688e-05	0.00287821	intron-variant	CORO2B	GRCh38.p7	15:68715318	AAGGCCTAGGTAAGT[A/G]GCCCCGAGGCTGCCA	10391
rs780016062	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68702067	GGCCAACATGATAAG[C/T]GGAAGGACAGATCAT	10391
rs780016981	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68567031	GTTCTGTGCTTCAGT[G/T]TTCTCATCTGTGAAG	10391
rs780017085	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68582389	GGGCCCTGAGCATGC[A/C]CAGGAGGTCAAGGTG	10391
rs780024001	snp	C/T			downstream-variant-500B	CORO2B	GRCh38.p7	15:68728166	GAACCACTGTTCTAC[C/T]GCTATTCAATAGATG	10391
rs780039077	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68689043	AACCTGATCCCCAGC[C/G]CCGAGCTCTTCCTTG	10391
rs780044728	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68646280	CGTGGGAGGTCACGC[A/G]CTTCAGGGAAAGTGC	10391
rs780072544	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68638472	AGGTAGTCCAAAGTC[A/G]TACAACTAACAAGTA	10391
rs780094252	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68557487	GTCTATCCAAGGTCA[C/T]GGCAGAGCTGAGGTT	10391
rs780126549	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68687850	AAACCCACTCACAAG[A/G]CAACTAACCCACTCC	10391
rs780193002	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68647411	GAAAAAGAACCCGAC[C/T]GGACACGGTGGCTCA	10391
rs780196683	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68682052	AACCCAGTCCCATGC[C/T]CCGTCCCTGGATAGC	10391
rs780199795	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68710371	AGAGTCTCCTAGAAG[G/T]ATGTGGCATGTGAAG	10391
rs780214715	snp	C/T			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726215	CTGCCACCCCAGGAG[C/T]CAGGCTTCCCCTCAG	10391
rs780222180	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68679522	AGGGAGGAAGCTAAC[C/T]TGCATTTTGCAGATG	10391
rs780263811	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68636198	CTGTTAGTGTGATGA[A/G]CCAGGAGCAAGGGGA	10391
rs780284009	in-del	-/AG			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68727394	TCCCACTACGCACAA[-/AG]AGTTTATAAACACTG	10391
rs780292194	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68707523	ATATTCATCATGGAA[C/T]GGTCATACAACAGAT	10391
rs780294491	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68665600	AATATCCATGATCAT[A/G]GTTTACTTTTTGTAG	10391
rs780315668	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68678394	ATAACAGAGAAAAGA[A/C]AGCAGGCGGTGGTTC	10391
rs780367432	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68590113	CCTCAGGCCAGACCA[C/T]ATCACCAGCTTGAGA	10391
rs780371149	in-del	-/AGGCTGACCTGCCCA			intron-variant	CORO2B	GRCh38.p7	15:68576683	CATCCTTCTGGCTAG[-/AGGCTGACCTGCCCA]AGACAGCTGAGACAG	10391
rs780383570	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68597754	GAGGAACCTCGGGCA[A/G]AAGTCCAGCCTGCGG	10391
rs780432741	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654715	AAAAGCACTTAGCAC[A/G]TAGCCTGGCCCATAG	10391
rs780456389	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625740	ACCCCAAGTAGCTAG[A/G]ACTACAGGTGCACAC	10391
rs780457130	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68576831	TTTGTTCTTGGTGGC[A/C]TTAAATATTTGCTAA	10391
rs780468214	in-del	-/AA			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577727	CTACTCCGGTCTCAA[-/AA]AAAAAAAAAAAAAAA	10391
rs780480351	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68585448	ACCATGGGGTAGATT[C/G]TATTATCCATCCCAT	10391
rs780485321	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68725734	CAGTGGGAGGCCTGG[A/G]GGAATGTGAGGGCAC	10391
rs780493440	snp	A/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615960	TGCCCAGATGAGCAG[A/G]GTGGAGGAGGCTGCC	10391
rs780517935	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68672491	ACTATGTTGCCCAGG[C/T]TGATCTTGAACTCCT	10391
rs780571606	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68690874	TTCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTTA	10391
rs780614840	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68574616	GAGGTTATTAAGGTT[-/G]GAAGATAAAGGTGCC	10391
rs780641902	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68592149	CACACATCCACTCCA[C/G]ACTGCCAAGAGTTGT	10391
rs780657640	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68722050	GAGACACTGCGCCCA[A/G]CTATTTTCTTGTTTT	10391
rs780661771	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68611894	CTCCCACCTCAGCCT[C/G]CCAAGTAGCTGGGAC	10391
rs780665538	snp	A/G	1.72018e-05	0.00293268	intron-variant	CORO2B	GRCh38.p7	15:68719591	CCACAGGCCCTGGAA[A/G]AGCAAGACCTTTACA	10391
rs780672019	snp	G/T	1.65004e-05	0.00287227	missense	CORO2B	GRCh38.p7	15:68719440	TGTCTTTGAAAGAAG[G/T]CTATAAGAAGTCCTC	10391
rs780674567	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68697787	GTTGCTTCCTGGGCT[A/G]GGAAAGAGGCACAGG	10391
rs780708993	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68663494	CACGCGCACACACAC[A/G]CAGAAGAATTTCCTC	10391
rs780711884	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68717707	AGAAGAACTCAGACC[A/G]AATCTGCTGGCTCTT	10391
rs780719800	snp	C/T	1.65321e-05	0.00287502	intron-variant	CORO2B	GRCh38.p7	15:68695132	CTCTCTCTCTTTCTC[C/T]TCTGCAGACAGGCAG	10391
rs780723504	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68610639	CTATGTCTGCTTCTA[G/T]ACCTGAGTATATGTT	10391
rs780729926	in-del	-/G			intron-variant	CORO2B	GRCh38.p7	15:68560142	CTGGGGGCTGCCTGG[-/G]AAGATCCGGATATTG	10391
rs780740211	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68582504	GCTGATTTTATTCTT[C/T]AGGTTCTTCTGACTG	10391
rs780772199	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68694038	ATGGGGTTTCTCCAC[A/G]TTGGCCAGGCTGGTC	10391
rs780773362	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68654995	GTGCAGGGTCTCCAG[A/G]GAGGCATGACTGAGG	10391
rs780820813	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68623718	AGCAGCAGCGGGTGG[C/G]AGGGCAGGCAGGGCT	10391
rs780826527	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68651609	CAGTCTTGTCCCTAC[A/G]CTGAATGGCTCCAGA	10391
rs780837409	in-del	-/TTT			intron-variant	CORO2B	GRCh38.p7	15:68703152	TCTTTCTTTTTTTCT[-/TTT]TTTTTTTTTTTTTTT	10391
rs780845361	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68632995	GATCCCCTTTACATT[C/T]CTCTCTGACCTCTTC	10391
rs780854151	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68601349	TTGAGGGTTCCACCC[A/G]TCCCTGGGCCTCATT	10391
rs780863196	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68668368	GAGTTGTGTGAGCCA[G/T]TCAGGAGACAAACAA	10391
rs780876927	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68690383	ACCCCCATATTTCTT[-/A]ATTACATGCCTTTAC	10391
rs780910830	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68633997	GTTATCCTGAGAGTC[A/G]GTCAGGGCATGTCAC	10391
rs780944963	snp	G/T	3.32486e-05	0.00407715	intron-variant	CORO2B	GRCh38.p7	15:68711726	AACCCTACATTTTTT[G/T]AGATTGAAGGGGAAG	10391
rs781004138	snp	A/G			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68640046	CCTCCTCTCTCTGGC[A/G]GAGTAGGGAGGAGTC	10391
rs781013486	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68625885	GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC	10391
rs781030685	snp	A/G	1.65479e-05	0.0028764	missense	CORO2B	GRCh38.p7	15:68714019	CCAGGTGGAACACAA[A/G]ACAGATTGCCCTCTG	10391
rs781033221	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68568433	CACTATTGCCCTTTA[C/T]CCTCTGAGAGGTTGT	10391
rs781033847	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68575502	ACCGCGTCTGGCTAA[-/T]TTTGGTATGTTTAGT	10391
rs781049320	snp	A/G	0.000480654	0.015495	intron-variant	CORO2B	GRCh38.p7	15:68579282	CTGTCACAAAGGTAA[A/G]CGCCGCTCGCCCGCC	10391
rs781062171	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68644882	GACCCTACAACCTTT[-/C]TAGAAAGTGGGGTGG	10391
rs781067771	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68590625	CCACTTCGCTTAGAA[A/C]CCACTATAGAATTCC	10391
rs781098669	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68669379	CAGTTGGGCAGATTC[C/T]CTAAAGGGAACAGGG	10391
rs781107604	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68599282	CTGATGAGATAGTTA[A/T]ATCTGAACATGTCTT	10391
rs781117668	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68708020	GCCACCAAAGGGGAT[A/G]ACAATGGGGATGGGA	10391
rs781123740	snp	A/G	1.87693e-05	0.00306338	intron-variant	CORO2B	GRCh38.p7	15:68718671	AGTTTCTGGGACCCC[A/G]TGGAGCCACATGTGT	10391
rs781130465	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68618201	CATGATATGCACTCT[A/G]TTTTCTAGTCTTTTC	10391
rs781134238	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68720048	GGGCCTTGTCCATGT[C/T]CCCCAGCGGTATTTC	10391
rs781143385	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68700231	CGGCAAAGCTGCTGT[A/G]TGTGCCAGGCACTGT	10391
rs781156133	in-del	-/CAAAAATA			intron-variant	CORO2B	GRCh38.p7	15:68717151	TCTAAACCCTGTCAC[-/CAAAAATA]CAAAAAGTACCTGGG	10391
rs781184743	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68566853	CCAAAGCTACCAAAC[A/G]CAGCGTCATGTGCAA	10391
rs781205281	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68679743	CACTACCCCAGCCCC[C/T]GAGGATCAACCAACC	10391
rs781226393	in-del	-/AAAAA			intron-variant	CORO2B	GRCh38.p7	15:68597628	TGTTTCCCCCCCATC[-/AAAAA]AAAAAAAATAAATAA	10391
rs781254407	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68698490	TAAACAAGACATCCA[G/T]GGTTTGTGTCCAAGA	10391
rs781282942	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68710536	CTCCCACAGGCAGAG[A/C]GATGGTCTCCTTCCT	10391
rs781285211	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68670558	GTGATAAGGAACTAA[G/T]ACACAGAATTAATAT	10391
rs781294901	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68657383	TTAGCCAGGTGTGGT[A/G]GCATATGCTAGTAGT	10391
rs781304830	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68625835	GTCTCAAACTCCTGA[G/T]CTCAAGCAATCTGCC	10391
rs781339255	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68693048	ATATCAACGCTCTCC[A/G]AATCCTTTTTCTCTA	10391
rs781340309	snp	A/G	1.68732e-05	0.00290454	missense	CORO2B	GRCh38.p7	15:68718799	CCCATCTCCATGATC[A/G]TGCCCCGGAGGGTAA	10391
rs781387879	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68668003	CAGTAATCACCCACA[C/T]CTGTTGAACACGTAC	10391
rs781422063	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68626792	AGTTAAGCAGCAAGG[G/T]CTGAGAACCGCTGCT	10391
rs781425248	snp	C/T	1.65971e-05	0.00288067	missense	CORO2B	GRCh38.p7	15:68725861	CTTCGAATGTTCTTC[C/T]GGCAGCAGGATGAGA	10391
rs781428472	snp	A/C	1.9645e-05	0.00313403	missense	CORO2B	GRCh38.p7	15:68710772	GCGGGCTGAAGCGGA[A/C]CATGACGGAGGCGCT	10391
rs781443178	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68616722	CAAGGGCCCCGAGAG[A/C]TGGGTCTTGCCTCTT	10391
rs781471489	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68654783	ACTGTTACCCATCTC[C/G]AGGCCACCCCATCCT	10391
rs781480924	in-del	-/TCAGAGCAGTGGGGCCAGATGGAGGG			intron-variant	CORO2B	GRCh38.p7	15:68580384	GGGTCAGATGGAGGG[-/TCAGAGCAGTGGGGCCAGATGGAGGG]TTGGGGTGCAAGTGA	10391
rs781481058	in-del	-/C	0.000216321	0.0103978	intron-variant	CORO2B	GRCh38.p7	15:68725820	CTGGGCCCTCCTTGG[-/C]CCCCTCTCTTCCTCC	10391
rs781495628	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68637381	TGTGTCCACCTTTCC[C/T]GGGTGGAGGGGGAAC	10391
rs781509107	in-del	-/A			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577724	GACTACTCCGGTCTC[-/A]AAAAAAAAAAAAAAA	10391
rs781525935	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68586623	ATAAGGACACAGGCA[C/T]AGAGAAGCTAAGTCA	10391
rs781535073	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68592630	TTCTGGTTCAAGTCC[C/T]ACCTCTCTGCATCTA	10391
rs781544743	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68673274	GGCACAATGGCTCAC[A/G]TCTATGATACCAGCA	10391
rs781578495	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68643241	GTGTCCTGATGAGGA[C/G]CCAGTGCTTGGGGAA	10391
rs781599006	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68562608	AAAATTACTCATTGT[G/T]TCTTGAAATTCAAAT	10391
rs781603333	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68674400	TAACTCGGGACTGAA[A/G]CCAGCGAATGCCCCA	10391
rs781606637	snp	A/G			upstream-variant-2KB, intron-variant	CORO2B	GRCh38.p7	15:68615998	GAACACCTACTGTGC[A/G]CCAGACCTGCTGGGT	10391
rs781619992	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68561568	CAGGGAGGGAGGCAG[A/G]CAGCTGGGTGGGAGG	10391
rs781626682	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68604926	CAAGACCAATCTGGC[C/T]AACATAGTGAAACCC	10391
rs781689899	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68573926	CTTTCTGGAGGAGGC[A/G]ATACCTAAGGAAAGA	10391
rs781696851	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68678032	GAGGCTGCCTTGCCC[C/T]TCCATAATTAACAGG	10391
rs781697989	snp	C/T	1.66018e-05	0.00288108	synonymous-codon	CORO2B	GRCh38.p7	15:68725939	CAGCTCCAGCTGGAA[C/T]TGAAAAACTTGCGCA	10391
rs781698457	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68675724	AGTGCTTAGAAAACA[C/T]TAACACATTGTAGGT	10391
rs781700207	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68716644	GGGGCTACTTCACCC[C/T]GGTGGTCAGGGAAGG	10391
rs781707292	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68722071	TTCTTGTTTTTAAAA[G/T]AACTCTACTCTTTGA	10391
rs781740017	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68568290	CATCCCCACAACAAT[A/G]CTTCATTTTCTCATC	10391
rs781777297	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68656571	GCAAATGCTTCAGAA[C/T]CATCCCATTTCCCAC	10391
rs781780080	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68686608	AAATGTATATAAATT[A/G]CTTAACACGGCCAGG	10391
rs796081861	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68689787	GGCAGAGGCATTTTG[C/T]TTGTTCTTTAATTTT	10391
rs796085600	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68697130	ATGGATTGTGGATGG[A/G]TGGATGGATGGATTG	10391
rs796087365	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68705084	CATGTGGTGCCAACT[C/G]TTTGCTATAGCCATG	10391
rs796108592	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68576165	CGCAAAAAAAAAAAA[A/G]AAAAAAAAAAAGAAA	10391
rs796117056	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703147	CCATATCTTTCTTTT[C/T]TTCTTTTTTTTTTTT	10391
rs796133029	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68610585	TCCTCCAGCATCCTG[C/T]GCGTTTAAATTTGTA	10391
rs796144848	in-del	-/GT			intron-variant	CORO2B	GRCh38.p7	15:68619755	TGAGTGCGTGCATGC[-/GT]GTGTGTGTGTGCACG	10391
rs796154260	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68691401	GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG	10391
rs796162371	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68709465	TTTTTTCGTGTTTTT[G/T]TTTTTTTTTTTTTTT	10391
rs796173325	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68635690	CACATGGAGGAAAAG[C/T]TGGGCCCAGAGGAGG	10391
rs796176817	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68711407	TATAGAACTCAATGA[C/G]CCCCTCCTGCACCCC	10391
rs796188050	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68679120	GCCTGGCACCGTGCT[C/G]GGTGTTGGGATACAG	10391
rs796190318	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68707760	GGGTCACCTTTCTAC[-/A]GTACATTTGGGGACA	10391
rs796196982	in-del	-/TT			intron-variant	CORO2B	GRCh38.p7	15:68703153	CTTTCTTTTTTTCTT[-/TT]TTTTTTTTTTTTTTT	10391
rs796213945	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68647984	AGTGAGCTATGATCA[C/T]TCCCCTGCACTCCAC	10391
rs796267422	in-del	CGTGAGTGTGTGTTGTGA/T			intron-variant	CORO2B	GRCh38.p7	15:68561906	CCTGTGAGCATGACC[CGTGAGTGTGTGTTGTGA/T]TGTGTACACATGCGT	10391
rs796272192	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68588450	TTGAAAAGTGAGCCA[A/G]ATAAAGCATCCAAAC	10391
rs796296817	in-del	GG/T			intron-variant	CORO2B	GRCh38.p7	15:68714267	TTTTCCAGAGTGGGG[GG/T]TGAGCTCCAGAGAGA	10391
rs796330292	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68653873	AGGAAAAAAAAAAAA[-/A]TGCCTGAATCTTCAT	10391
rs796334547	snp	A/T			intron-variant	CORO2B	GRCh38.p7	15:68562664	AGAGAAATGAGAAAA[A/T]TATAAAATACTTCGA	10391
rs796337588	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68703212	CTGTCATGCAGTGGC[A/G]CGATCTCAGCTCACT	10391
rs796354199	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68708125	AATGGTGCACCCAAG[G/T]GTGACCCCAAACCCT	10391
rs796356173	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68574260	GGAGCTTGGAAGCCT[A/G]ATGAGCTGAGGGGGC	10391
rs796372453	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68709150	TGAACATCTTCATGC[A/G]TGGAGATTTTTTGCT	10391
rs796375287	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68595962	CAGAGGCCAGGGCAG[C/T]GACGCCGTGGGGTGC	10391
rs796383778	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68717292	GCACTCCAACCTGGG[C/T]AACAGAGCCAGACTC	10391
rs796384463	in-del	-/CA			intron-variant	CORO2B	GRCh38.p7	15:68633714	CAACTTCTCCTTTCT[-/CA]CATTTGGGGCACTGA	10391
rs796403140	multinucleotide-polymorphism	CT/TC			intron-variant	CORO2B	GRCh38.p7	15:68688931	GGGCGTCCATGCCCT[CT/TC]TCCTGGGGCTGGGGA	10391
rs796412366	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68717311	GAGCCAGACTCTGTC[-/A]AAAAAAAAAAAAAAA	10391
rs796412543	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68626167	AAAATGTTCCTACTG[A/C]GTGCTGCTGTGAGGG	10391
rs796431051	in-del	-/A			intron-variant	CORO2B	GRCh38.p7	15:68721187	ACACCTGGCCCACTA[-/A]TCACTATTATTAATA	10391
rs796432568	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68580153	GAGGGTGATAATATG[G/T]GTCCTGGGTTGTGAC	10391
rs796445368	in-del	-/TT			intron-variant	CORO2B	GRCh38.p7	15:68660976	AATGTGTAATGAGTC[-/TT]TTTTTTTTTTTTCTG	10391
rs796452390	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68560471	GCTAATTAAAGACAA[-/T]TTTTTTTTGTAGAAA	10391
rs796453831	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68590357	GCTCTTCGGAGGCTG[-/C]CCCCCCATGCCCAGC	10391
rs796453862	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68681235	AAAAAAATTTTTTTT[-/T]GGAAAGAAAAGCTGA	10391
rs796481177	in-del	-/AA			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577725	GACTACTCCGGTCTC[-/AA]AAAAAAAAAAAAAAA	10391
rs796491080	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68582016	GGCCTGGCAAGTGGA[A/G]AAGAGGAAAGCAGAT	10391
rs796492715	in-del	AA/T			intron-variant	CORO2B	GRCh38.p7	15:68682195	CCCAACTGCCAAAAA[AA/T]CCTGCAGATAGTTAT	10391
rs796520858	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68618649	TAGCATATTTGCTGC[C/T]GAGGCGAGCACAAGG	10391
rs796527563	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68662844	CAGCTTCTTATAATA[C/G]ATTTGTATATATTTT	10391
rs796543366	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68646079	CACCTGGCCCACTCA[-/T]TTTTTTTTTTAATTG	10391
rs796556370	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68672383	TGGGATTACAGGCAT[A/G]AGCCAAGTACATAGA	10391
rs796559870	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68593762	GTGAGTTTGCTCTGA[C/G]GTGGCGAAGTGGGTG	10391
rs796560521	in-del	-/C			intron-variant	CORO2B	GRCh38.p7	15:68574050	CCTGTTGGACTTCAA[-/C]CTGAGGACACCAGGG	10391
rs796589123	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68605761	GGAGTCTCGCTGTGT[C/T]GCCCAGGCGGGAGTG	10391
rs796598282	in-del	-/AAGC			intron-variant	CORO2B	GRCh38.p7	15:68669188	GAAAAGAAAGAAAGG[-/AAGC]AAGCAAGCAAGCAAG	10391
rs796603222	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68674892	TATTATCTCCCACTA[C/T]ACTCTCTTTAGGGGT	10391
rs796610380	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68706368	AGCTTTCCAACAGCT[C/G]TGTGCCCCCACAGGC	10391
rs796613511	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68566051	TTGCATTTTGCACAC[C/T]GAAGTCAAGCAGTCC	10391
rs796626719	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68620368	TAAATAAACATGGTT[C/T]GGGTGATTTGTAGAA	10391
rs796658065	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68671560	CTGGTTCAGGGTCTC[A/G]TTTGGTTGCGTTAAA	10391
rs796689118	in-del	-/T			intron-variant	CORO2B	GRCh38.p7	15:68686021	GAGCTCCTACTTCTG[-/T]TTTTTTTTTTTTTTT	10391
rs796702645	multinucleotide-polymorphism	AAG/GTA			intron-variant	CORO2B	GRCh38.p7	15:68691486	AAAATTAGCCGGGCG[AAG/GTA]TGGCGGGCGCCTGTA	10391
rs796706459	multinucleotide-polymorphism	AC/CT			utr-variant-3-prime	CORO2B	GRCh38.p7	15:68726036	TCATCCCTTAACTTC[AC/CT]CCTTACCAGTGACCC	10391
rs796720263	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68659063	TTTAGGCAAAACCTT[C/T]ATGCAGTTGGACAGT	10391
rs796722792	snp	G/T			intron-variant	CORO2B	GRCh38.p7	15:68581673	AAGTCACCTCTGATG[G/T]AGATTGGGAGACTCT	10391
rs796727585	snp	C/G			intron-variant	CORO2B	GRCh38.p7	15:68648452	GAGATCAAGACCATC[C/G]TGGCTAACATGGTGA	10391
rs796750261	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68621809	TCTCCTAGGCTGGAG[A/G]ACAGTGGTGCAATCA	10391
rs796762818	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68717998	TGTAACTTGCCAAAG[A/G]ACTCCTAGATGGAAA	10391
rs796810956	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68659106	AGCAAAGGACCTGCA[A/G]TGGACGGTCTGCCTT	10391
rs796819517	in-del	-/AAA			intron-variant, upstream-variant-2KB	CORO2B	GRCh38.p7	15:68577744	AAAAAAAAAAAAAAA[-/AAA]TTGCACAATGACCCA	10391
rs796819948	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68611683	AAAGTATGATTTTTA[C/T]GCCTATATAATAGTT	10391
rs796859415	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68589819	GACCAACTAGGAGCG[A/C]CCTGACCAGAGGCCT	10391
rs796886429	snp	A/G			intron-variant	CORO2B	GRCh38.p7	15:68612223	ATGTACACATTGAAA[A/G]GGTCTAAAAGTAAAT	10391
rs796954857	in-del	-/AG			intron-variant	CORO2B	GRCh38.p7	15:68648048	AAAAAAAAAAAAAAA[-/AG]AGTCTGGGCATGGTG	10391
rs796959404	snp	A/C			intron-variant	CORO2B	GRCh38.p7	15:68576153	GTGAGACTACGTCGC[A/C]AAAAAAAAAAAAAAA	10391
rs796982216	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68703397	CTCAAGTGAACTGCC[C/T]GCCTGGGCCTCCCAA	10391
rs797010987	snp	C/T			intron-variant	CORO2B	GRCh38.p7	15:68648518	AGCCAGGTCTGGTGG[C/T]GGGCGCCTGTAGTCC	10391

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