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

MYNN

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1317082	snp	A/G	0.391583	0.206044	intron-variant	MYNN	GRCh38.p7	3:169779797	TCCCTCCAAATAAGT[A/G]TGTTGATTCTAGCTT	55892
rs1881966	snp	A/G	0.431473	0.171952	intron-variant	MYNN	GRCh38.p7	3:169778152	GGAGTTGAAGGCTGC[A/G]GTGAGTTATCATTAT	55892
rs1920120	snp	C/T	0.487933	0.0767327	intron-variant	MYNN	GRCh38.p7	3:169784392	AGATACATTTCTGTT[C/T]ATGAAAATGCTCAAG	55892
rs1920121	snp	A/G	0.0482946	0.147699	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787865	TGCCACTTTTCCCAC[A/G]TATTAATTTATTTCA	55892
rs1920122	snp	C/T	0.487558	0.0778863	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788353	TCTATGCATGTGTAT[C/T]AAGTTAAAATAGTGG	55892
rs1920123	snp	C/T	0.487558	0.0778863	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788385	TTTAAATACAATTTA[C/T]AAAGCATTAGAATGT	55892
rs2068178	snp	A/G	0.0755905	0.179113	missense	ACTRT3	GRCh38.p7	3:169767851	AAACCCGATTGTCTA[A/G]AGAAAGTTTACCAAC	55892
rs2141595	snp	C/T	0.496714	0.0404017	intron-variant	MYNN	GRCh38.p7	3:169785644	TCCGGGCAGAGAACA[C/T]TGTAGAGAGTCAGTG	55892
rs2251795	snp	A/T	0.408359	0.193449	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773941	TAGTGGTTTAAAAAA[A/T]TTTTTTGTAACATAA	55892
rs3046465	in-del	-/ATC	0.391583	0.206044	intron-variant	MYNN	GRCh38.p7	3:169778160	AGGCTGCGGTGAGTT[-/ATC]ATTATACCAGTGCAC	55892
rs3772188	snp	C/T	0.0479149	0.147179	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787159	CTAAATTTTTACGAG[C/T]GAAAATATGAAATTT	55892
rs3772190	snp	C/T	0.391397	0.206172	intron-variant	MYNN	GRCh38.p7	3:169782699	TAAAAGGCCCAAGTC[C/T]CCTTTTTCTTTTATT	55892
rs3821383	snp	C/T	0.488545	0.074807	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772158	CTCAAGTGATTATTA[C/T]CAAATTGAGAGGAAT	55892
rs3950296	snp	C/G	0.391583	0.206044	intron-variant	MYNN	GRCh38.p7	3:169775495	ATCTTTCCTGTCAGT[C/G]GCTATGTCTCCTTGA	55892
rs4618260	snp	A/C	1.64953e-05	0.00287182	missense	ACTRT3	GRCh38.p7	3:169767662	AGGTTGATCCCCCGG[A/C]AAGGATAATATTGGA	55892
rs7624848	snp	A/G	0	0	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786703	GAATATGGAATTGCT[A/G]AGATATCATTGGTAG	55892
rs7626989	snp	A/C			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771263	attatatttatatat[A/C]ataaatatataaaaa	55892
rs7634517	snp	C/G	0	0	intron-variant	MYNN	GRCh38.p7	3:169786280	GTGAGGAGGGCATAT[C/G]TACAAAAGAGAAACC	55892
rs7634698	snp	A/G			synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169786468	TACTTTGAGTGAACA[A/G]GATTCCATACAAAAA	55892
rs9811216	snp	C/T	0.472803	0.113397	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769713	CCGTGCTCCTCATGT[C/T]ACCGCCCGCTATTGC	55892
rs9822885	snp	A/G	0.461202	0.133767	intron-variant	ACTRT3	GRCh38.p7	3:169768356	CACTGGGTAACTGTA[A/G]GGAAAGCAATAAGAT	55892
rs9823758	snp	A/G	0.0722614	0.17581	intron-variant	ACTRT3	GRCh38.p7	3:169768944	CAATTGAAGAGAATA[A/G]CCCAAGTGACAAAAG	55892
rs9826466	snp	A/C/T	0.00755907	0.0610114	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772313	aaacacACTAAAAAA[A/C/T]CCCtttttttttttt	55892
rs9833597	snp	A/G			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770457	ttatatttatatatc[A/G]taaatataaatatat	55892
rs9833619	snp	A/G			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770494	ttatatttatatatc[A/G]taaatataaatatat	55892
rs9833638	snp	A/G			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770531	ttatatttatatatC[A/G]taaatataaatatat	55892
rs9833790	snp	A/G			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770568	ttatatttatatatc[A/G]taaatatataaaaat	55892
rs9838385	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771155	ataaatatataaaaa[A/T]ttatatttatatatc	55892
rs9838401	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771186	ataaatatataaaaa[A/T]ttatatttatatatc	55892
rs9838416	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771217	ataaatatataaaaa[A/T]ttatatttatatatc	55892
rs9838561	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771305	atataataaatatat[A/T]aaaaattatgtttat	55892
rs9840387	snp	G/T	0.0123036	0.0774623	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787442	TTTATGTTTTATTCC[G/T]TTCTAAAATATTGGA	55892
rs9853966	snp	C/T	0.0123036	0.0774623	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786977	TGCATTTTAGAATTG[C/T]CCTTCATTTACTAAA	55892
rs9855337	snp	A/G	0.084364	0.187256	intron-variant	MYNN	GRCh38.p7	3:169774702	TGTTTTTATAAAGAA[A/G]TCAGTATCACTGATT	55892
rs9860874	snp	A/C	0.489837	0.0705577	intron-variant	ACTRT3	GRCh38.p7	3:169768483	CACAGCCTCTCACAG[A/C]AGGTAAGTGTCAGCC	55892
rs9866116	snp	A/G	0.497907	0.0322805	intron-variant	MYNN	GRCh38.p7	3:169776839	CTCCCGAGTAGCTGG[A/G]ATTACAGGCACCCGC	55892
rs9866557	snp	A/G	0.0119091	0.0762411	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769581	ACGGGCTCGGCCGGG[A/G]CCGAGTGCCTGGAAC	55892
rs9866776	snp	A/C	0.488363	0.0753851	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769863	CCAGAAGAGCTATAA[A/C]AGCAGTTTTATTTTC	55892
rs9874233	snp	A/G	0.0119091	0.0762411	intron-variant	MYNN	GRCh38.p7	3:169783224	TCATATAAAAATCAA[A/G]TTCCTTGCCCAAATC	55892
rs9880210	snp	G/T	0.0119091	0.0762411	intron-variant	MYNN	GRCh38.p7	3:169777102	AATTAGAGACCAAAA[G/T]ATCTTTTTTAGTGGC	55892
rs10576565	in-del	-/AA	0.0119091	0.0762411	intron-variant	MYNN	GRCh38.p7	3:169775366	GGAGGGAATAAAAGC[-/AA]AGAGAAACTGATTAA	55892
rs10681957	in-del	-/TTT			intron-variant	MYNN	GRCh38.p7	3:169776695	TTTTTTTTTTTTTTT[-/TTT]TTGAGATGGAGTCTC	55892
rs10936599	snp	C/T	0.404747	0.19635	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774313	GCAGTATTCGCACCA[C/T]TGTGAGCACCTTTTA	55892
rs11293618	in-del	-/A			upstream-variant-2KB	MYNN	GRCh38.p7	3:169771962	CCTTTCCAGGGAGAC[-/A]AAAAAAAAAAAGGCC	55892
rs11336818	in-del	-/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772317	ACACTAAAAAATCCC[-/T]TTTTTTTTTTTTTTT	55892
rs11456214	in-del	-/A			intron-variant	MYNN	GRCh38.p7	3:169784913	AAAAAAAAAAAAAAA[-/A]CTTGAAACATTTCCT	55892
rs11553294	snp	G/T	0	0	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774367	AGCAGGTTTTCTCTG[G/T]GACTGTACCATAGTG	55892
rs11714841	snp	A/G	0.0197644	0.0974247	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786433	GCAGATAAAACTCTA[A/G]ACTCCAGTGCAGAGG	55892
rs12637087	snp	C/G/T	0.000166289	0.00911711	synonymous-codon, missense	ACTRT3	GRCh38.p7	3:169769383	GAGTTCTAGCCCGCC[C/G/T]TGGGCCGCGCGGCTC	55892
rs12637184	snp	A/G	0.394538	0.203982	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769649	CAGAGTCCTGGGGGC[A/G]CAGGCAGGGGGTCGG	55892
rs13314293	snp	A/G	0.0116702	0.075491	intron-variant	MYNN	GRCh38.p7	3:169778743	TTTGATCAGAATATT[A/G]TCATGTAGCCTTGTT	55892
rs16847890	snp	C/T	0.0134861	0.0810011	intron-variant	MYNN	GRCh38.p7	3:169777803	GTAACTCTCACATCA[C/T]GAACACTCCAGCTAA	55892
rs16854368	snp	C/G/T	0.0486741	0.148216	intron-variant	MYNN	GRCh38.p7	3:169783337	CATTTACTTGGATCA[C/G/T]TGAAAATACCTCTAA	55892
rs17568472	snp	A/G	0.00911815	0.0669024	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774448	TGAGTATTTTGGTGC[A/G]ATCTACAGAAGCACT	55892
rs17850177	snp	C/G			missense	ACTRT3	GRCh38.p7	3:169768317	GATCTCCATGTCCTC[C/G]CATGAAGTAATGAGA	55892
rs28371163	snp	A/C			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771325	ATTATGTTTATATAT[A/C]ATAAATATAAAAATT	55892
rs28465436	snp	A/C	0.433673	0.1696	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771294	ATTATGTTTATATAT[A/C]ATAAATATATAAAAA	55892
rs28635281	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771310	ATAAATATATAAAAA[A/T]TTATGTTTATATATA	55892
rs28649851	snp	A/G	0.466412	0.125164	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771524	TATATAAAAATTTAT[A/G]TTTATATATAATAAA	55892
rs34022516	snp	A/G	0.0195694	0.0969626	intron-variant	MYNN	GRCh38.p7	3:169779641	GAGTACTTAGCACAC[A/G]CTACTTGTGACCAGA	55892
rs34026158	in-del	-/C			intron-variant	MYNN	GRCh38.p7	3:169775831	AAATCTTTCCCTCCC[-/C]TTTTATATTGTAACT	55892
rs34273285	snp	C/G	0.026644	0.112304	missense	ACTRT3	GRCh38.p7	3:169767800	CAGCTCCATGACCAG[C/G]TCTTTTCTTGTCCAG	55892
rs34321597	snp	A/C			intron-variant	MYNN	GRCh38.p7	3:169775700	GAAAAAATAGAAAAA[A/C]CAAAAAAGAAACACC	55892
rs34384341	in-del	-/A/ATA	0.00199481	0.0315187	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771333	ATATATAATAAATAT[-/A/ATA]AAAAATTTGTTTATA	55892
rs34594906	snp	A/G	0.00979952	0.0693089	intron-variant	MYNN	GRCh38.p7	3:169779611	ACTGTGACTAATATA[A/G]TGTATTTTTATAGAG	55892
rs34684730	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787157	TAAAATTTCATATTT[-/T]CGCTCGTAAAAATTT	55892
rs34847803	in-del	-/A	0.394721	0.203852	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774228	CGTTGATGAGAACTT[-/A]ACGGTTACTGATTTA	55892
rs34931136	snp	C/T	0.000115545	0.00759994	synonymous-codon	ACTRT3	GRCh38.p7	3:169768161	TCTGGGTGTTCCTGC[C/T]TTCTATATGTCCATC	55892
rs35100673	snp	C/T	0.0547245	0.156101	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772149	ATTATATTCATTCCT[C/T]TCAATTTGATAATAA	55892
rs35197165	in-del	-/CT/TC	0.0478135	0.14704	intron-variant	MYNN	GRCh38.p7	3:169779769	CCCTAATGCATCAAC[-/CT/TC]TCCTTATACCATTTT	55892
rs35270580	snp	C/T	0.00439002	0.0466448	synonymous-codon	ACTRT3	GRCh38.p7	3:169767885	TGTGGCAATGAACTA[C/T]GAAGAGGAAATGGCC	55892
rs35283637	snp	C/G			downstream-variant-500B	MYNN	GRCh38.p7	3:169789983	ACATGTGCCATGTTG[C/G]TGTGCTGCACCCATT	55892
rs35294030	snp	C/T	0.00134076	0.025857	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779040	GCCTTCTTCTTCTTT[C/T]TCGTTTGAGATGACT	55892
rs35379604	in-del	-/CAT			intron-variant	MYNN	GRCh38.p7	3:169778162	GCTGCAGTGAGTTAT[-/CAT]TATACCAGTGCACTC	55892
rs35406871	snp	A/G	0.0262422	0.111501	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169782609	AGTGATAAGAGAACT[A/G]GAGACAGCAAATGCC	55892
rs35419455	snp	A/G/T	0.022753	0.104207	missense	ACTRT3	GRCh38.p7	3:169768201	TGGCCAACCGGCAAC[A/G/T]GATCACGGAAATGTT	55892
rs35446936	snp	A/G	0.406641	0.194842	intron-variant	ACTRT3	GRCh38.p7	3:169768720	TTTTTAGTAGAGACG[A/G]GGTTTCACCGTGTTA	55892
rs35505613	in-del	-/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771866	GAAAGGATGGCTTTT[-/T]CGCGGCTGAATAACG	55892
rs35580600	in-del	-/A/TA/TGTTTATATATAATAAATATAAAAATT	0.0678856	0.17156	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771340	ATAAATATAAAAATT[lengthTooLong]TGTTTATATATAATA	55892
rs35943960	in-del	-/A	0.5	0	upstream-variant-2KB	MYNN	GRCh38.p7	3:169771973	AGACAAAAAAAAAAA[-/A]GGCCACCCAAAGGAA	55892
rs55656133	snp	A/G			missense	ACTRT3	GRCh38.p7	3:169767676	GCAAGGATAATATTG[A/G]AAAAGAAGGAATTCC	55892
rs55735727	snp	A/T	0.410905	0.191336	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770360	GAAATATATATATTT[A/T]TATTTATTATATGTA	55892
rs56312325	in-del	-/AATATA			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770607	TATATCATAAATATA[-/AATATA]TAAAAATTTATATTT	55892
rs56355715	in-del	-/AATATA			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770576	TATATCATAAATATA[-/AATATA]TAAAAATTTATATTT	55892
rs56651288	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770678	AAAAATTTATATTTA[G/T]ATATCATATATAAAA	55892
rs56651316	snp	A/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770714	TATTTAGATATCATA[A/T]ATAAAAATTTATATT	55892
rs56651385	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770705	AAAAATTTATATTTA[G/T]ATATCATATATAAAA	55892
rs56651412	snp	A/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770687	TATTTAGATATCATA[A/T]ATAAAAATTTATATT	55892
rs57684934	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772419	CTGAGGGAAGCCTTA[A/G]CTTAATGTATGCCGG	55892
rs58083088	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169785118	TCCAGAAATGTTTAA[A/G]AGGAAATAGGGAAAC	55892
rs58580234	snp	A/T			intron-variant	MYNN	GRCh38.p7	3:169782689	TAAAGTTATAAATAA[A/T]AGAAAAAGGGGACTT	55892
rs61087913	in-del	-/T	0	0	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772337	TTTTTTTTTTTTTTT[-/T]CCTTCGCTTGGAAGA	55892
rs61745452	snp	C/T	1.64936e-05	0.00287168	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779257	ACAAGATATTGTGCA[C/T]ACTGTTACAGTGAAA	55892
rs62293395	snp	G/T	0.5	0	intron-variant	ACTRT3	GRCh38.p7	3:169768546	TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTCGCT	55892
rs62293396	snp	A/C/G	0.00318978	0.0398085	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772222	TACAAAACCCTCTCC[A/C/G]AAGTGGGGTTTCCGT	55892
rs62293397	snp	A/T	0.00199481	0.0315187	intron-variant	MYNN	GRCh38.p7	3:169780257	TAGAGACTGGGTTTC[A/T]CCATGTTAGCCAGGA	55892
rs71300477	in-del	-/C	0.5	0	intron-variant	MYNN	GRCh38.p7	3:169785081	TTCATGATAACACCA[-/C]CCCCCCCCCCCTTTT	55892
rs71306647	snp	C/T	0.5	0	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769550	CGCCGCCTCCTGTCT[C/T]TGAGCCGCTCTAGCT	55892
rs71306648	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772242	GGGGTTTCCGTAGTG[G/T]AGTGGTTATCACGTT	55892
rs71306649	snp	A/C	0.5	0	intron-variant	MYNN	GRCh38.p7	3:169776990	TGCACCCGGCCTTGA[A/C]CAATTAATGTATGAC	55892
rs73879124	snp	G/T	0.0865458	0.189163	intron-variant	MYNN	GRCh38.p7	3:169784375	TGTTTGTTTTAGTTT[G/T]CAGATACATTTCTGT	55892
rs73879125	snp	A/G	0.0858192	0.188533	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787377	AATGAATTTTAAGTA[A/G]ATATTTGGTGTTTTT	55892
rs74310670	in-del	-/A			intron-variant	MYNN	GRCh38.p7	3:169778495	GGGTTTTAAAAAAAA[-/A]AGCCAGAAAATTTAA	55892
rs75277808	snp	A/G	0.12932	0.218944	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789636	GTACTACAGGTGCGC[A/G]CCACCACACCTGACT	55892
rs75435018	snp	C/T	0.0314385	0.121371	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772722	TTAAAAATCTTCTGG[C/T]CCAGACGCAGGAAAA	55892
rs75734604	snp	A/G	0.0314385	0.121371	intron-variant	MYNN	GRCh38.p7	3:169786165	TGTGATTAAGCCGAT[A/G]TAACAGCTCACCCTG	55892
rs76020348	snp	G/T	0	0	intron-variant	ACTRT3	GRCh38.p7	3:169768543	TTTTTTTTTTTTTTT[G/T]TGGAGACAGAGTCTC	55892
rs76057740	snp	A/T	0.00398564	0.0444627	intron-variant	MYNN	GRCh38.p7	3:169776084	CTGGCCTGCAATTTA[A/T]TGGTTTCCCTTTCTC	55892
rs76253854	snp	A/G	0.5	0	intron-variant	MYNN	GRCh38.p7	3:169779834	TATTTAACAGAGACA[A/G]AGACATTAAAACTGA	55892
rs76417879	snp	A/C	0	0	upstream-variant-2KB	MYNN	GRCh38.p7	3:169771964	TTTCCAGGGAGACAA[A/C]AAAAAAAAAGGCCAC	55892
rs76458720	snp	A/G	0.5	0	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772818	CTTTCGTGCATCCCA[A/G]ACTTCTGTCACCAGG	55892
rs76993079	snp	C/T	0.029116	0.117091	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788307	CACCTTTGTATGATG[C/T]AAACAATATTTGATT	55892
rs77065455	snp	A/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772311	GGAAACACACTAAAA[A/T]ATCCCTTTTTTTTTT	55892
rs77604843	snp	A/T	1.70243e-05	0.00291751	intron-variant	MYNN	GRCh38.p7	3:169784718	ATTCTGGTAAATGCT[A/T]GTGTTTTGTTTGCTT	55892
rs77643779	snp	A/G	0.0648419	0.167978	intron-variant	MYNN	GRCh38.p7	3:169781217	CAAAGATGATTCTGA[A/G]GTTTTGGGCCTGAAC	55892
rs78044405	snp	A/G	0.0260105	0.111035	intron-variant	MYNN	GRCh38.p7	3:169780035	AAAGTATGAGCACCT[A/G]TTGGTACGTTTACAT	55892
rs78057436	snp	C/G/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773323	ATGGCCCCAGAACCT[C/G/T]CCGCACTGCCACGGG	55892
rs78105580	snp	C/G	0.0221141	0.102801	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773905	CTGTTCTGCCCCTAT[C/G]TGTCCCAAGAGATCA	55892
rs78107829	snp	A/C/T	0.000808567	0.0200908	intron-variant	ACTRT3	GRCh38.p7	3:169768375	AAGCAATAAGATCAA[A/C/T]GACAGCTTTTTATTT	55892
rs78698796	snp	A/G	0.0138799	0.0821421	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788312	TTGTATGATGCAAAC[A/G]ATATTTGATTATTTT	55892
rs78706446	snp	A/G	0.031825	0.122064	intron-variant	ACTRT3	GRCh38.p7	3:169768991	TTCTTAAATGAATTC[A/G]TTCGATAACTTTATA	55892
rs78787316	snp	A/T			intron-variant	MYNN	GRCh38.p7	3:169779674	TTGGTATATTTTTCT[A/T]TTCATCAAAGTATTT	55892
rs79000471	snp	A/G			upstream-variant-2KB	MYNN	GRCh38.p7	3:169771973	AGACAAAAAAAAAAA[A/G]GGCCACCCAAAGGAA	55892
rs79352432	snp	A/G	0.0023933	0.0345097	downstream-variant-500B	MYNN	GRCh38.p7	3:169790055	TCCCCTCTCCCCCCA[A/G]CTACCTAGAACTTGA	55892
rs79600202	snp	G/T	0.5	0	intron-variant	ACTRT3	GRCh38.p7	3:169768544	TTTTTTTTTTTTTTT[G/T]GGAGACAGAGTCTCG	55892
rs79852109	snp	A/T	0.5	0	intron-variant	MYNN	GRCh38.p7	3:169779833	GTATTTAACAGAGAC[A/T]AAGACATTAAAACTG	55892
rs79992152	snp	C/G	0.0197687	0.0974348	intron-variant	MYNN	GRCh38.p7	3:169785280	CACTAGGCCCTTCTG[C/G]TGTGTAAATACTTAA	55892
rs80272070	snp	A/G	0.0314385	0.121371	intron-variant	MYNN	GRCh38.p7	3:169784141	TTTATATTCTGACGC[A/G]CTTTAGTTTACACCA	55892
rs111215366	snp	A/G			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770637	TATATATCATATATA[A/G]AAATTTATATTTATA	55892
rs111215425	snp	A/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770696	ATCATATATAAAAAT[A/T]TATATTTAGATATCA	55892
rs111215428	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771121	ATCATAAATATATAA[A/T]AATTTATATTTATAT	55892
rs111286999	snp	G/T	0.0349115	0.127424	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770108	AATGCTTTGTTGTGT[G/T]TCTTCCTGTGATTTC	55892
rs111325249	snp	A/G	0.5	0	intron-variant	MYNN	GRCh38.p7	3:169778676	CATTCTGCTTCATTA[A/G]GTCTTTAAAATACAT	55892
rs111431310	snp	C/G	0.0248432	0.108648	intron-variant	MYNN	GRCh38.p7	3:169786216	ATTTTTTTAAATGGA[C/G]TTGGTGCTTGAACTT	55892
rs111767038	snp	C/T	0.5	0	intron-variant	MYNN	GRCh38.p7	3:169782726	TTTAGCGAAGTAGAT[C/T]GGAAACTTTGTAGTT	55892
rs112478138	snp	A/G	0	0	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773138	AGAGCGCCAGACGCT[A/G]ACTGCCGGCACCAGA	55892
rs112511892	snp	G/T	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169785079	AAAAAAAGGGGGGGG[G/T]GGTGGTGTTATCATG	55892
rs113006697	snp	A/G	0.5	0	intron-variant	MYNN	GRCh38.p7	3:169786252	TGAGGCCCAGATTGA[A/G]TTTACATAGATAGTG	55892
rs113007230	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774192	TGTTTAAGTTATGTC[C/T]TCTGTCCCTTCCCTC	55892
rs113135556	snp	C/T	0.444444	0.157135	intron-variant	MYNN	GRCh38.p7	3:169780182	GCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	55892
rs113291870	snp	A/G	0.5	0	missense, nc-transcript-variant, intron-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169778800	TTCATCAGGCTGCTG[A/G]CTATCTCAAAGTGGA	55892
rs113373034	snp	C/T	0.0322114	0.122752	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772216	GGACTTTACAAAACC[C/T]TCTCCAAAGTGGGGT	55892
rs113374430	snp	C/T	0.0244538	0.107838	intron-variant	ACTRT3	GRCh38.p7	3:169768672	AGCTGGGACTACAGG[C/T]GCGCGCCACCACGCC	55892
rs113551265	snp	C/T			intron-variant	ACTRT3	GRCh38.p7	3:169768674	CTGGGACTACAGGCG[C/T]GCGCCACCACGCCCG	55892
rs114146302	snp	A/C	0.0314385	0.121371	intron-variant	MYNN	GRCh38.p7	3:169783159	CTCCTTTATTAATAT[A/C]GTAGATAGCAAGAAT	55892
rs114340092	snp	A/G	0.0162398	0.0886349	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773646	GAGTGGGAGCTGGGC[A/G]GAGGGCAGGGCGGCA	55892
rs114547598	snp	A/C/G/T	0.0178356	0.0929414	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772215	AGGACTTTACAAAAC[A/C/G/T]CTCTCCAAAGTGGGG	55892
rs114862028	snp	C/T	0.00716266	0.059414	intron-variant	MYNN	GRCh38.p7	3:169778208	AGAAGAATACCCCAT[C/T]TCAAAACAGAAAAAA	55892
rs114892675	snp	C/T	0.0193772	0.0965046	intron-variant	MYNN	GRCh38.p7	3:169775505	TCAGTCGCTATGTCT[C/T]CTTGAGCATGATGCA	55892
rs114937201	snp	A/G	0.0314385	0.121371	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773115	GGGCCTCGGCGCAGA[A/G]CCCCGGCAGAGCGCC	55892
rs114956060	snp	C/T	0.0146672	0.084371	upstream-variant-2KB	MYNN	GRCh38.p7	3:169771940	GGAAAGGATGTGTAA[C/T]AAAACGCCTTTCCAG	55892
rs115126604	snp	A/G	0.0648419	0.167978	intron-variant	MYNN	GRCh38.p7	3:169777762	TTTGACTAGAATATT[A/G]AACAAGGTGGCTTAA	55892
rs115269486	snp	A/C	0.0146672	0.084371	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169769962	GGAAAAATGAGACTT[A/C]AGAGGAGAAAGTTGT	55892
rs115760243	snp	A/T	0.0479149	0.147179	intron-variant	MYNN	GRCh38.p7	3:169782301	TTGATAATAAGAAAT[A/T]TTTGTTTTTGGCAGT	55892
rs115766258	snp	C/T	0.0314385	0.121371	intron-variant	ACTRT3	GRCh38.p7	3:169769179	CTCCTTTGGGGTCCT[C/T]TCCTGCCCCCCGACA	55892
rs115797213	snp	C/T	0.040671	0.13668	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772306	CGGGCGGAAACACAC[C/T]AAAAAATCCCTTTTT	55892
rs116151092	snp	A/G	0.0410537	0.137264	intron-variant	MYNN	GRCh38.p7	3:169781577	ACTTTATGAGTTCTG[A/G]GAGATGGGTGAGAAC	55892
rs116162796	snp	C/T	0.0134861	0.0810011	intron-variant	MYNN	GRCh38.p7	3:169780878	ACAATGTTAACACGT[C/T]CAAGGAACCACAAGG	55892
rs116573309	snp	C/T	0.00795532	0.062565	intron-variant	MYNN	GRCh38.p7	3:169775931	TTCTTGTGTAAGAAG[C/T]ATCCAGTGGGGGGAG	55892
rs117375742	snp	A/C	0.0256316	0.110334	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169769932	GGGAGTTCTAGAATT[A/C]GCCCTTGAAACTGGG	55892
rs137960491	snp	A/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783424	TTATTTGTAATTGAT[A/T]AATATTATATTGGTA	55892
rs138358992	snp	C/T	0.0205511	0.0992634	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770095	CTGTACCTTGGGCAA[C/T]GCTTTGTTGTGTTTC	55892
rs138434633	snp	C/T	0.00835141	0.0640778	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772221	TTACAAAACCCTCTC[C/T]AAAGTGGGGTTTCCG	55892
rs138456601	snp	A/C	0.00676609	0.0577691	intron-variant	MYNN	GRCh38.p7	3:169776681	TATGAATTACCATTT[A/C]AATGTTGAACAAATT	55892
rs138718489	snp	C/T	0.0119091	0.0762411	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771627	AGGCTGAAGGACGTG[C/T]CTGTCTTTTTGCAGG	55892
rs139017220	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773101	GGTGCTGTGCTGCCG[C/G]GCCTCGGCGCAGAGC	55892
rs139065735	snp	C/T	3.30038e-05	0.00406212	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169778889	TCTTCTACAGAGATA[C/T]CTAGTATTACTGGAA	55892
rs139138415	snp	C/G	0.00953873	0.0683987	intron-variant	MYNN	GRCh38.p7	3:169780337	TGCTGGGATTATAGG[C/G]GTGAGCCACCGAGCC	55892
rs139138672	snp	A/G	0.000479264	0.0154726	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169780645	TGCTCAGAAATGTCA[A/G]CTAGTCTTCCATAGT	55892
rs139332496	snp	G/T	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787014	AGTTAATGTGATTCA[G/T]TTGTGACCTGTGGGA	55892
rs139521740	snp	A/G	4.96118e-05	0.0049803	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779074	CAACTCCCCGAAAAC[A/G]GGGCAGAATAAAACA	55892
rs139881990	in-del	-/GT/GTGT	0.166747	0.2383	intron-variant	MYNN	GRCh38.p7	3:169777480	ATTTGAGGGTAAGGG[-/GT/GTGT]GTGTGTGTGTGTGTG	55892
rs139959878	snp	C/T	0.00795532	0.062565	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772295	CGGTTCGAAACCGGG[C/T]GGAAACACACTAAAA	55892
rs140432446	snp	A/C	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775573	AGATGGTAATAACTA[A/C]CTTGAGGCTAAATAA	55892
rs140519498	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773516	TCTCTAGAGCCTGGG[C/T]CATCAGAGGGCAGGC	55892
rs140560623	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169780219	CCTGCCACCAAGTCC[A/G]GCTAATTTTTTTGTA	55892
rs141198623	snp	C/G/T	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787570	TTTCTAGATATAAAC[C/G/T]TAATGCATACTAGAA	55892
rs141203272	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772430	CTTAGCTTAATGTAT[A/G]CCGGTCCTTCAAAAG	55892
rs141406872	snp	A/G	1.65343e-05	0.00287521	synonymous-codon	ACTRT3	GRCh38.p7	3:169768290	GTTATAGTCATAGAT[A/G]TGCTTCCACATGATC	55892
rs141541380	snp	A/C			intron-variant	MYNN	GRCh38.p7	3:169777584	AGCTAAGAAAGTTGA[A/C]CCCCCCAAAGATGCT	55892
rs141609462	snp	C/T	0.000329766	0.0128364	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779358	AGAGTCCTTATGAGG[C/T]GGAGAACTCCGGGGA	55892
rs142065065	snp	A/G	0.000973445	0.0220403	missense	ACTRT3	GRCh38.p7	3:169768153	ACAGCCTGGATGGAC[A/G]TATAGAAGGCAGGAA	55892
rs142106924	snp	G/T	0.0154538	0.0865337	downstream-variant-500B	MYNN	GRCh38.p7	3:169789950	TGTGCACAGCATGCA[G/T]GTTTGTTACATATGT	55892
rs142145413	snp	A/T	0.00438332	0.0466095	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769824	ATTCAACTCTAACCC[A/T]TCACAAGTGCATTTC	55892
rs142166727	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772604	ATAATGTACAGCCTA[A/G]AAGGAAAGATCAAAG	55892
rs142790452	snp	A/G	0.00677111	0.0577902	synonymous-codon	ACTRT3	GRCh38.p7	3:169767681	GATAATATTGGAAAA[A/G]AAGGAATTCCTCAGG	55892
rs142875546	snp	A/G	0.000414274	0.0143863	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779012	AATCCTAAACAAGGC[A/G]CGTTAGCGAAAAAGT	55892
rs142921997	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772234	TCCAAAGTGGGGTTT[C/T]CGTAGTGTAGTGGTT	55892
rs142927555	snp	A/T	0.0103295	0.0711199	intron-variant	MYNN	GRCh38.p7	3:169784879	TTTTTGCAGAAACAT[A/T]CACTCTGGATTTTTC	55892
rs142931874	snp	A/T	3.29832e-05	0.00406085	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786470	CTTTGAGTGAACAGG[A/T]TTCCATACAAAAAAG	55892
rs142962214	snp	C/T	0.00318978	0.0398085	intron-variant	MYNN	GRCh38.p7	3:169776764	GCTGGAGTGCAATGG[C/T]GTGATCTCGGCTCAC	55892
rs143160556	in-del	-/A			intron-variant	MYNN	GRCh38.p7	3:169778488	GGTTTTAAAAAAAAA[-/A]GCCAGAAAATTTAAC	55892
rs143284410	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169774998	TGTGCACTACCACAC[C/T]TGGCTAATTTTTGTA	55892
rs143421780	snp	A/C	0.00318978	0.0398085	intron-variant	MYNN	GRCh38.p7	3:169783865	AAGGAATAGGTAATA[A/C]CAAGATAACATCAGA	55892
rs143898480	snp	A/C/T	1.66142e-05	0.00288216	missense, stop-gained, nc-transcript-variant	MYNN	GRCh38.p7	3:169780712	GATGTATGCAACTTA[A/C/T]AGTTTGCAACTTCTA	55892
rs143938595	snp	C/T	0.000198522	0.009961	missense	ACTRT3	GRCh38.p7	3:169769393	CCGCCCTGGGCCGCG[C/T]GGCTCTGGCCCTTGG	55892
rs144286621	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787060	GCCCTCATAATTTAA[A/G]CAAAATCCACGATAG	55892
rs144366076	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774209	CTGTCCCTTCCCTCA[A/C]TGAACGTTGATGAGA	55892
rs144408911	in-del	-/C			intron-variant	MYNN	GRCh38.p7	3:169776691	CATTTCAATGTTGAA[-/C]AAATTTTTTTTTTTT	55892
rs144483224	snp	A/T	0.0119091	0.0762411	intron-variant	MYNN	GRCh38.p7	3:169778425	GTTGCTATCTGAAGA[A/T]GCCTCAGGATGAATG	55892
rs145155594	snp	A/G	0.0134861	0.0810011	intron-variant	MYNN	GRCh38.p7	3:169782838	GAATAATACAAGGTG[A/G]GTGAAATAAATTATA	55892
rs145615297	snp	C/G/T	0.00795532	0.062565	intron-variant	MYNN	GRCh38.p7	3:169781911	TTTGTTTTGTTTTTG[C/G/T]TTTTTTTTTAATATG	55892
rs145630145	snp	C/G	0.00199481	0.0315187	intron-variant	ACTRT3	GRCh38.p7	3:169768764	CGAACTCCTGACCTC[C/G]TGATCCGCCCTGCTC	55892
rs145743523	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781160	TAAAGTTAGAAATAA[C/T]AGAATTTGCAAACAG	55892
rs145804135	in-del	-/T			intron-variant	MYNN	GRCh38.p7	3:169776222	TTCAGTCTCTTTTGG[-/T]ACATATCTTTCCTGG	55892
rs145847218	snp	C/T	0.00914312	0.0669923	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788901	ATATATTTAGTTGTA[C/T]CTGGTATCATTCTAA	55892
rs145903956	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169775682	AATTCCACATTTCTC[A/G]GAGAAAAAATAGAAA	55892
rs145973490	snp	C/G	0.00597247	0.0543191	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772267	CACGTTCGCCTAACA[C/G]GCGAAAGGTCCCCGG	55892
rs146178757	snp	A/G	8.2479e-05	0.00642127	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779239	GGAAAATACTTTTCC[A/G]GCACAAGATATTGTG	55892
rs146383374	in-del	-/AAAT	0.0475351	0.146656	intron-variant	MYNN	GRCh38.p7	3:169781114	TGGCAGCAGTGAAAG[-/AAAT]AAGTAGTAGTAGATT	55892
rs146411700	snp	A/G	1.67351e-05	0.00289263	synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169778822	CAAAGTGGAAGAGGT[A/G]GTCACTAAATGCAAA	55892
rs146547200	snp	C/T	0.0154538	0.0865337	intron-variant	MYNN	GRCh38.p7	3:169782212	GAAAATAATTGCCTG[C/T]AGTATTAGGGGCCCA	55892
rs146558159	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787469	TGGAGATGAGGAAAA[C/T]GTACTTGAGTTTTGA	55892
rs146706191	in-del	-/ATA	0.0640965	0.167152	intron-variant	MYNN	GRCh38.p7	3:169784525	CCAAATTTAAACACT[-/ATA]ATAATTTTTGCCTTG	55892
rs146844941	snp	G/T	0.000269505	0.0116052	missense	ACTRT3	GRCh38.p7	3:169769394	CGCCCTGGGCCGCGC[G/T]GCTCTGGCCCTTGGC	55892
rs147067353	snp	A/C	0.0205511	0.0992634	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770085	ATTATTGTTTCTGTA[A/C]CTTGGGCAATGCTTT	55892
rs147152426	snp	C/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169784247	TTGCCAGGTACCTGA[C/G]AGCAGAAACCATGAT	55892
rs147165329	snp	A/T			missense, nc-transcript-variant, intron-variant	MYNN	GRCh38.p7	3:169783518	TGTGGGAAAAGTTTT[A/T]TTTCCTCAGGAGAGC	55892
rs147220696	snp	A/C	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169779732	TTGTAATTGTAACCA[A/C]GTATTTAATGGCTGT	55892
rs147398947	snp	C/T	1.6483e-05	0.00287076	synonymous-codon	ACTRT3	GRCh38.p7	3:169767750	ATCAATGCCAGGGGC[C/T]TCAAGGTTCATATGA	55892
rs147424091	snp	C/T	0.0154538	0.0865337	intron-variant	MYNN	GRCh38.p7	3:169785788	ATCATGTCAACACTT[C/T]AGAGTAACGGAAGCA	55892
rs147441397	snp	C/T	0.000447401	0.0149499	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779019	AACAAGGCGCGTTAG[C/T]GAAAAAGTCATCTCA	55892
rs147633219	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773199	CTGCGAGCTAGCGAG[C/G]CCTCAGCTCTCGTAT	55892
rs147694345	snp	A/G	0.000313808	0.0125222	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774516	AGGCTGATGGATTTC[A/G]GAAACTGTTGGAGTT	55892
rs147834358	snp	A/G	0.0648419	0.167978	intron-variant	MYNN	GRCh38.p7	3:169780301	CTGAACTCGTGATCC[A/G]CCCGCCTCCGCCTTC	55892
rs148032854	snp	A/G	1.65701e-05	0.00287833	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779029	GTTAGCGAAAAAGTC[A/G]TCTCAAACGAAAAAG	55892
rs148139182	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169789705	GCTGGTCTCGAACTC[A/C]TGACCTCAGGTGATC	55892
rs148357625	snp	C/T	0.0154538	0.0865337	intron-variant	MYNN	GRCh38.p7	3:169782940	TTTATAAAAACCTTT[C/T]CAGCTTCCTAAAGGG	55892
rs148459961	snp	A/G	0.00716266	0.059414	intron-variant	MYNN	GRCh38.p7	3:169785847	AAAAGTACATCTTTA[A/G]TCAGTGTGCTGATTG	55892
rs148598914	snp	C/T	1.65091e-05	0.00287303	missense	ACTRT3	GRCh38.p7	3:169768139	CAAAGAGAGCCAGCA[C/T]AGCCTGGATGGACAT	55892
rs148915764	snp	A/T	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768941	TGTCAATTGAAGAGA[A/T]TAACCCAAGTGACAA	55892
rs148970778	snp	A/G	3.3042e-05	0.00406447	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169786444	TCTAGACTCCAGTGC[A/G]GAGGATCATACTTTG	55892
rs148982711	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789606	ATTCTCCGGCCTCAG[C/T]CTCCTGAGTAGCTGG	55892
rs149111479	in-del	-/C	0.0193772	0.0965046	intron-variant	MYNN	GRCh38.p7	3:169778267	CTACTGAATTTGAAT[-/C]CTACATTTAACAAGA	55892
rs149177057	snp	A/G	0.0644693	0.167566	intron-variant	MYNN	GRCh38.p7	3:169774939	TGCCTCCCGGGTTCA[A/G]GCGATTCTCCCACCT	55892
rs149280999	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169778278	TGAATCTACATTTAA[C/T]AAGATTCCCGGGTGA	55892
rs149441489	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771741	GTCTGATTCTGCATA[C/T]ATCTGTAGAGAATTT	55892
rs149700988	snp	A/G	1.64974e-05	0.00287201	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779226	TGACATCAGTTGTGG[A/G]AAATACTTTTCCAGC	55892
rs149804512	snp	A/G	0	0	intron-variant	MYNN	GRCh38.p7	3:169780348	TAGGCGTGAGCCACC[A/G]AGCCCAGCCCTAGAT	55892
rs149964314	snp	A/T	0.0244538	0.107838	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773197	CGCTGCGAGCTAGCG[A/T]GCCCTCAGCTCTCGT	55892
rs150417121	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774400	TGGGGAATTCCAGTT[C/T]AAAGCTCATAGGAAT	55892
rs150524698	snp	C/G	0.000711785	0.0188517	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779055	AAAAGAAGAAGAAGG[C/G]TTTCAACTCCCCGAA	55892
rs150665901	in-del	-/CT	0.0648419	0.167978	intron-variant	MYNN	GRCh38.p7	3:169779766	GCCCTAATGCATCAA[-/CT]CTCCTTATACCATTT	55892
rs150730028	snp	C/T	0.00716266	0.059414	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772526	TTATGGAAGCCTTGC[C/T]ACGTGGAACATGTGT	55892
rs150852192	snp	C/T	3.40466e-05	0.00412579	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786691	TGACTTTGTAAGGAA[C/T]ATGGAATTGCTAAGA	55892
rs151055732	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786530	CTTCTGATATGACTT[C/T]ACCATTAGCTCTTCC	55892
rs151255743	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169775426	TATGAAAGTGAACAT[A/G]AATAGACTGTTCATA	55892
rs180758909	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771279	ATAAATATATAAAAA[A/T]TTATGTTTATATATA	55892
rs180766591	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787577	ATATAAACTTAATGC[A/G]TACTAGAAATCACTT	55892
rs180882469	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770813	AAAAATTTATATTTA[G/T]ATATCATAAATAAAA	55892
rs180891437	snp	G/T	0.0023933	0.0345097	intron-variant	MYNN	GRCh38.p7	3:169782296	ATGTTTTGATAATAA[G/T]AAATATTTGTTTTTG	55892
rs181218292	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771248	ATAAATATATAAAAA[A/T]TTATATTTATATATC	55892
rs181230864	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777216	CAAGTTTAATTAGAA[A/G]ATGATGAGAACATGG	55892
rs181243046	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787182	AAATTTAGGCGCTGA[A/G]TAAGAATTGTGCTAT	55892
rs181536004	snp	A/T	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169780944	GGGGACTACTAGGAA[A/T]TAAGGTCAGACTCGT	55892
rs181567272	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788367	TCAAGTTAAAATAGT[G/T]GGTTTAAATACAATT	55892
rs181763042	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169776415	CTCTTGGACAGGTTA[C/T]TTTATTTCTTTGGAC	55892
rs181850575	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772262	GTTATCACGTTCGCC[C/T]AACACGCGAAAGGTC	55892
rs182029936	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770867	AAAAATTTATATTTA[G/T]ATATCATAAATAAAA	55892
rs182142201	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777971	TGGTGGCTCACGCTT[A/G]TAATCCTAGCACTTT	55892
rs182325318	snp	C/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169782943	ATAAAAACCTTTTCA[C/G]CTTCCTAAAGGGTCA	55892
rs182358599	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770979	AAAAATTTATATTTA[G/T]ATATCATAAATATAT	55892
rs182364796	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785195	ACAAGTTTTGAGTCT[A/G]TTGGTTAAAGTGAAT	55892
rs182444236	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788708	TGGCTAAGATTGATT[C/G]AGCTTTTCTTGATCA	55892
rs182448399	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769583	GGGCTCGGCCGGGGC[C/G]GAGTGCCTGGAACGC	55892
rs182478645	snp	A/C			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771352	AATTTGTTTATATAT[A/C]ATAAATATAAAAATT	55892
rs182687445	snp	A/G	0.127599	0.217986	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771493	TATATAAAAATTTAT[A/G]TTTATATATAATAAA	55892
rs182747817	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	MYNN	GRCh38.p7	3:169772837	TCTGTCACCAGGTAA[A/G]GGCATCTTGGAAGCT	55892
rs182762745	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770921	AAAAATTTATATTTA[G/T]ATATCATAAATAAAA	55892
rs182770063	snp	C/G	0.000500759	0.0158155	intron-variant	MYNN	GRCh38.p7	3:169783437	ATAAATATTATATTG[C/G]TATAGTACACCACTT	55892
rs183167186	snp	A/T	0.00279162	0.0372561	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772052	GAAGAAAGTGCGTGC[A/T]GATTCAAGCTTTTGA	55892
rs183188973	snp	A/C/G	4.95334e-05	0.00497641	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779126	TTAGAGAATGCATCT[A/C/G]TTGAATTATTCCTAG	55892
rs183294365	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773869	TTTTGGTGACTTGAG[A/C]GCAGTTTTTAAAAAC	55892
rs183487979	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770562	AAAAATTTATATTTA[G/T]ATATCATAAATATAT	55892
rs183493803	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169774787	TGACACGTTTATTTA[C/T]TGAAACAAAGCCTGT	55892
rs183494308	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169779888	TCAGGCCAATTTTCA[A/G]ATATTGCCAACACTT	55892
rs183628043	snp	G/T	0.00358779	0.0422022	intron-variant	MYNN	GRCh38.p7	3:169778707	TGAAGTATATATGCA[G/T]CTCTGTTTCGAAAGT	55892
rs183840043	snp	A/T	0.000798403	0.0199641	intron-variant	ACTRT3	GRCh38.p7	3:169768746	TGTTAGCCACGATGG[A/T]CTCGAACTCCTGACC	55892
rs183922204	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787414	TCAAAGACAGTTTCA[A/G]AATTTGATTCAGTTT	55892
rs184228704	snp	A/G	0.00676609	0.0577691	intron-variant	MYNN	GRCh38.p7	3:169781203	GTCTGGAAGAGAGTC[A/G]AAGATGATTCTGAGG	55892
rs184262347	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772235	CCAAAGTGGGGTTTC[C/G/T]GTAGTGTAGTGGTTA	55892
rs184266795	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770759	AAAAATTTATATTTA[G/T]ATATCATATATAAAA	55892
rs184348781	snp	A/G			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771222	TATATAAAAAATTAT[A/G]TTTATATATCATAAA	55892
rs184355458	snp	C/G/T	0.00018681	0.00966281	intron-variant	MYNN	GRCh38.p7	3:169786402	ATGTAGATTTTTTTT[C/G/T]CCTTCCATTCTAGGT	55892
rs184515528	snp	C/T	0.0178098	0.0926698	intron-variant	MYNN	GRCh38.p7	3:169775681	TAATTCCACATTTCT[C/T]GGAGAAAAAATAGAA	55892
rs184610952	snp	A/G			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771253	TATATAAAAAATTAT[A/G]TTTATATATCATAAA	55892
rs184784660	snp	A/C			intron-variant	MYNN	GRCh38.p7	3:169776106	CCCTTTCTCTCAATT[A/C]ACTATGCAAAACAAA	55892
rs184859438	snp	C/G/T	0.000798403	0.0199641	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772218	ACTTTACAAAACCCT[C/G/T]TCCAAAGTGGGGTTT	55892
rs185292987	snp	A/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770822	TATTTAGATATCATA[A/T]ATAAAAATTTATATT	55892
rs185296576	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169780338	GCTGGGATTATAGGC[A/G]TGAGCCACCGAGCCC	55892
rs185299015	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169782407	AAAACTTTATGAATT[C/T]TTGCTATATAGACTG	55892
rs185416254	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777444	AAACCATATTTAGGG[A/G]AAAAAATCAAGTAGG	55892
rs185453739	snp	G/T	0.114387	0.210022	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770651	AAAAATTTATATTTA[G/T]ATATCATATATAAAA	55892
rs185476396	snp	A/G			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771191	TATATAAAAAATTAT[A/G]TTTATATATCATAAA	55892
rs185766307	snp	A/C			intron-variant	MYNN	GRCh38.p7	3:169785323	TTAAGTTAGAAACAT[A/C]TAAAAACTGCAGTAA	55892
rs185857314	snp	A/G	0.401924	0.198543	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771315	TATATAAAAAATTAT[A/G]TTTATATATAATAAA	55892
rs185865824	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788535	TTATTTATATCTTCG[C/T]TAATCCAAGCATCTA	55892
rs186004146	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772271	TTCGCCTAACACGCG[A/G]AAGGTCCCCGGTTCG	55892
rs186035358	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169773011	GGCCCCGAGGAAGGG[G/T]AGGATGATGGGAGAA	55892
rs186231088	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788874	GCTATGCTATTATTT[A/G]TCATAATATGCATAT	55892
rs186441801	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772520	ATGTTTTTATGGAAG[A/C]CTTGCCACGTGGAAC	55892
rs186458305	snp	C/T	1.65263e-05	0.00287452	synonymous-codon	ACTRT3	GRCh38.p7	3:169768263	TGGGCCATCACACGG[C/T]TTCAGCTTTAGGTTA	55892
rs186465331	snp	C/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169778187	GTGCACTCCTGCTTG[C/G]GCAACAGAAGAATAC	55892
rs186591868	snp	C/G			intron-variant	MYNN	GRCh38.p7	3:169785267	TTATTCGACATGACA[C/G]TAGGCCCTTCTGGTG	55892
rs186790905	snp	C/T	0	0	intron-variant	MYNN	GRCh38.p7	3:169776469	AAATGAGGATTATAA[C/T]AGATTTCATAGGCAT	55892
rs186892759	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169783283	ATAAAGTTTTAATAT[A/G]TGAAAACTTATGAAC	55892
rs186900139	snp	A/C	0.0134861	0.0810011	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770305	TATATTTATATATTT[A/C]TAAAATATATATTTA	55892
rs186909924	snp	A/G	1.64901e-05	0.00287137	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779337	TGTCTAATATAGCCA[A/G]CGTCAAGAGTCCTTA	55892
rs187047327	snp	A/T	0.400147	0.19989	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770930	TATTTAGATATCATA[A/T]ATAAAAATTTATATT	55892
rs187052986	snp	C/T	1.64912e-05	0.00287147	missense, nc-transcript-variant, intron-variant	MYNN	GRCh38.p7	3:169783494	GAAAAACCATACATA[C/T]GTGGTATTTGTGGGA	55892
rs187077550	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770894	AAAAATTTATATTTA[G/T]ATATCATAAATAAAA	55892
rs187269028	snp	A/G			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771284	TATATAAAAAATTAT[A/G]TTTATATATAATAAA	55892
rs187458032	snp	A/G			upstream-variant-2KB	MYNN	GRCh38.p7	3:169772172	GATAATAATCACTTG[A/G]GAATTGCGAATTGAC	55892
rs187473156	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787890	ATTTCACTGCCTGAT[A/C]TTTGGATATGAAATT	55892
rs187779073	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB, intron-variant	MYNN	GRCh38.p7	3:169774063	ATTCACCGTCACTTA[C/T]TGATGTGTCCAAAGG	55892
rs187779587	snp	G/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780010	TTTTGCATGTCCTCT[G/T]CCTGGTTGTAAAGTA	55892
rs187988377	snp	A/T			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771359	TTATATATAATAAAT[A/T]TAAAAATTTATGTTT	55892
rs187991985	snp	A/T	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169775224	TAAGATGCTTACTGA[A/T]GTCACTGCATTAACA	55892
rs188095651	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775809	GATGTGCATGTATAC[A/G]TTAAGCAAAATCTTT	55892
rs188243190	snp	C/G			upstream-variant-2KB	MYNN	GRCh38.p7	3:169771961	GCCTTTCCAGGGAGA[C/G]AAAAAAAAAAAAGGC	55892
rs188331652	snp	C/G	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768961	CCAAGTGACAAAAGG[C/G]ACCATGAGTTAATAT	55892
rs188513065	snp	A/G	0.0023933	0.0345097	intron-variant	MYNN	GRCh38.p7	3:169782058	GAATTGATGGATTCA[A/G]ATGAACTGTCACCCT	55892
rs188552001	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770786	AAAAATTTATATTTA[G/T]ATATCATATATAAAA	55892
rs188625148	snp	C/G/T	4.94868e-05	0.00497407	synonymous-codon, missense, nc-transcript-variant, intron-variant	MYNN	GRCh38.p7	3:169778861	GGAAGATTTTGCTTT[C/G/T]ATTGCTAATCCTTCT	55892
rs188632661	snp	A/C	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785433	TACTCAAAGCACTTA[A/C]AACCTGGTGTGCGAG	55892
rs188823864	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771606	CATTCGCTACTCTTG[A/C]TTTTTAGGCTGAAGG	55892
rs188848862	snp	A/C			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771232	ATTATATTTATATAT[A/C]ATAAATATATAAAAA	55892
rs188859352	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787158	AAAATTTCATATTTT[C/T]GCTCGTAAAAATTTA	55892
rs188861372	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772279	ACACGCGAAAGGTCC[C/T]CGGTTCGAAACCGGG	55892
rs188954224	snp	A/C			upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771201	ATTATATTTATATAT[A/C]ATAAATATATAAAAA	55892
rs189068269	snp	G/T	0.0755793	0.179102	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770593	AAAAATTTATATTTA[G/T]ATATCATAAATATAT	55892
rs189202294	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169776258	GGGGAGCTAATTCCT[C/T]GAGTTCAGCTAGAAA	55892
rs189371343	snp	A/C			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787508	GGTAAGCCTCTCTTA[A/C]TCCTGTTATGCACTT	55892
rs189742983	snp	C/T	0.00199481	0.0315187	intron-variant	MYNN	GRCh38.p7	3:169777020	CTTCCTGCTAACTTA[C/T]ATTGGTCTTAAAGGC	55892
rs189923815	snp	G/T	0.139564	0.224285	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770948	AAAAATTTATATTTA[G/T]ATATCATAAATATAT	55892
rs189929280	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777804	TAACTCTCACATCAC[A/G]AACACTCCAGCTAAT	55892
rs189932273	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169784140	CTTTATATTCTGACG[C/T]GCTTTAGTTTACACC	55892
rs190228933	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788587	TGACGTCATAATTCT[A/G]TAAGGGCAATAGTTG	55892
rs190847293	snp	A/T	0.0189856	0.0955633	intron-variant	MYNN	GRCh38.p7	3:169778487	TGTGTTCTAGGGTTT[A/T]AAAAAAAAAGCCAGA	55892
rs190873131	snp	A/G	0.117188	0.211804	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771462	TATATAAAAATTTAT[A/G]TTTATATATAATAAA	55892
rs191083210	snp	A/G			downstream-variant-500B	MYNN	GRCh38.p7	3:169790018	CGTCATTTACATTAG[A/G]TATTCCTCCTAATGC	55892
rs191165537	snp	C/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773305	GGCCGGCGCCGGACC[C/G]CCATGGCCCCAGAAC	55892
rs191273345	snp	A/C			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772616	CTAGAAGGAAAGATC[A/C]AAGTGTAAAAGTGGT	55892
rs191325753	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779076	ACTCCCCGAAAACAG[A/G]GCAGAATAAAACAGT	55892
rs191351162	snp	A/T	0.00199481	0.0315187	intron-variant	MYNN	GRCh38.p7	3:169779651	CACACACTACTTGTG[A/T]CCAGAATTTGGTATA	55892
rs191674933	snp	A/T	0.40263	0.198	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770903	TATTTAGATATCATA[A/T]ATAAAAATTTATATT	55892
rs191786284	snp	A/G	3.52952e-05	0.00420075	intron-variant	ACTRT3	GRCh38.p7	3:169768369	TAAGGAAAGCAATAA[A/G]ATCAATGACAGCTTT	55892
rs191829657	snp	A/C	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788136	TTTCTCTATTTGGGA[A/C]CCAAGTCATAAGAAC	55892
rs191868429	snp	C/T			upstream-variant-2KB	MYNN	GRCh38.p7	3:169772214	AAGGACTTTACAAAA[C/T]CCTCTCCAAAGTGGG	55892
rs191971640	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169783351	ACTGAAAATACCTCT[A/G]AAGTACAATATAGAG	55892
rs192097971	snp	A/C	0.00398564	0.0444627	intron-variant	MYNN	GRCh38.p7	3:169782799	GCACATATTTGTTAA[A/C]TATAAAAGCTGACTT	55892
rs192213312	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774169	AGGATTTTCAAGGGG[A/G]CTAAAATTGTTTAAG	55892
rs192357295	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772225	AAAACCCTCTCCAAA[C/G/T]TGGGGTTTCCGTAGT	55892
rs192459083	snp	G/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770840	AAAAATTTATATTTA[G/T]ATATCATAAATAAAA	55892
rs192502092	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771751	GCATACATCTGTAGA[A/G]AATTTGAAAACAAGC	55892
rs192622713	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169776073	GTGAATTTTGGCTGG[C/T]CTGCAATTTAATGGT	55892
rs192906908	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169775292	GTGTGTCTCCCCTGT[A/G]TAACGAACCATATAA	55892
rs192978488	snp	G/T	0.0103295	0.0711199	intron-variant	ACTRT3	GRCh38.p7	3:169769094	TGTGGCCCGTGCGTT[G/T]GTAGTAATTCCAGCT	55892
rs193095236	snp	G/T	0.0770498	0.180522	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770624	AAAAATTTATATTTA[G/T]ATATCATATATAAAA	55892
rs193125371	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169785310	AACATCGTAAGTATT[A/G]AGTTAGAAACATCTA	55892
rs193163154	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169785914	ATATATGAAAGTGCC[A/G]TACATACTGTTCTGA	55892
rs193241419	snp	A/G	0.00478085	0.0486577	intron-variant	MYNN	GRCh38.p7	3:169780305	ACTCGTGATCCGCCC[A/G]CCTCCGCCTTCCAAA	55892
rs199548793	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774199	GTTATGTCCTCTGTC[C/T]CTTCCCTCACTGAAC	55892
rs199670531	snp	A/G	6.60611e-05	0.00574684	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779095	GAATAAAACAGTGCA[A/G]TATCCCAGTGACATC	55892
rs199681359	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772364	AAGAAAGCGTGAGAT[C/T]ACGCTTTGTTTTCTT	55892
rs199700748	snp	C/T	0.0120424	0.0766564	intron-variant	MYNN	GRCh38.p7	3:169783705	ATAAATATCAACTTA[C/T]TTGCTTATTTTGTTT	55892
rs199825440	in-del	-/TATA			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770359	CGAAATATATATATT[-/TATA]TTTATTATATGTATA	55892
rs199911803	snp	A/T	0.000593433	0.0172152	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779324	AAAGAACACTCTATG[A/T]CTAATATAGCCAGCG	55892
rs199962374	snp	A/C/G	3.29784e-05	0.00406058	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779399	CAGAGGTATTCCAAG[A/C/G]CCAAGCCAATGTGTA	55892
rs199983098	in-del	-/A			intron-variant	MYNN	GRCh38.p7	3:169785062	ACTATGGTTATTATG[-/A]AAAAAAAAGGGGGGG	55892
rs199991577	snp	A/G	0.00199797	0.0315435	synonymous-codon	ACTRT3	GRCh38.p7	3:169769428	GCCGATAATGTTCGG[A/G]TAGATAAACTGGGGC	55892
rs200012068	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169778162	GCTGCGGTGAGTTAT[C/T]ATTATACCAGTGCAC	55892
rs200309187	snp	A/C/G	3.33201e-05	0.00408156	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774552	ACACAGGAACTTTAA[A/C/G]TCTTGACAGGTAAAG	55892
rs200320591	snp	A/T	0.000186241	0.00964809	intron-variant	ACTRT3	GRCh38.p7	3:169768387	CAATGACAGCTTTTT[A/T]TTTTTCTAGTTTCTA	55892
rs200476514	in-del	-/A	0.0023933	0.0345097	intron-variant	MYNN	GRCh38.p7	3:169785559	TCTGAGGTAAGTACT[-/A]AAAAAAACTTAATTT	55892
rs200617627	snp	C/G	5.00421e-05	0.00500186	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786651	GTATTCAGAACCACA[C/G]TTGATTTTTTTACAA	55892
rs200643422	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169779368	TGAGGCGGAGAACTC[C/T]GGGGAAGAGCTGGAT	55892
rs200707283	snp	A/G	0.00716266	0.059414	intron-variant	MYNN	GRCh38.p7	3:169777391	TTTTCTGGCTTATAC[A/G]TACAACAGAGAGGGA	55892
rs200754674	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772408	TGTTTTTTTTTCTGA[C/G]GGAAGCCTTAGCTTA	55892
rs200829478	snp	A/G	1.65007e-05	0.00287229	synonymous-codon, nc-transcript-variant, splice-acceptor-variant	MYNN	GRCh38.p7	3:169778882	TAATCCTTCTTCTAC[A/G]GAGATATCTAGTATT	55892
rs200854017	snp	A/G			intron-variant	ACTRT3	GRCh38.p7	3:169768796	GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA	55892
rs200868149	in-del	-/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772394	TTGTTGTTTGTTTTG[-/T]TTTTTTTTTCTGAGG	55892
rs200952289	snp	C/T	1.65135e-05	0.00287341	missense	ACTRT3	GRCh38.p7	3:169768121	CAGTAGTGAAGCCAG[C/T]AGCAAAGAGAGCCAG	55892
rs201069814	snp	C/G/T	3.31649e-05	0.00407204	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786431	GTGCAGATAAAACTC[C/G/T]AGACTCCAGTGCAGA	55892
rs201072433	in-del	-/T			intron-variant	MYNN	GRCh38.p7	3:169785079	AAAAAAGGGGGGGGG[-/T]GGTGGTGTTATCATG	55892
rs201205431	snp	A/G	0.000939745	0.0216562	intron-variant	ACTRT3	GRCh38.p7	3:169768357	ACTGGGTAACTGTAA[A/G]GAAAGCAATAAGATC	55892
rs201352850	snp	C/G	3.29489e-05	0.00405874	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774451	GTATTTTGGTGCGAT[C/G]TACAGAAGCACTTCT	55892
rs201569520	snp	A/C	0.00697547	0.0586436	intron-variant	MYNN	GRCh38.p7	3:169775774	ATATATTAATTAATT[A/C]TTTTCCAGATCTCTG	55892
rs201678146	snp	C/T	1.64776e-05	0.00287028	missense	ACTRT3	GRCh38.p7	3:169767878	GTTTCTTGGCCATTT[C/T]CTCTTCGTAGTTCAT	55892
rs201851716	snp	C/T	0.000185081	0.00961801	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786673	TTTTTACAACAATTA[C/T]ACTGACTTTGTAAGG	55892
rs201860864	snp	A/G	3.29826e-05	0.00406082	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779274	CTGTTACAGTGAAAC[A/G]GAAACGTGGAAAATC	55892
rs201870444	snp	C/T	0.000593051	0.0172097	missense	ACTRT3	GRCh38.p7	3:169767802	GGACAAGAAAAGAGC[C/T]GGTCATGGAGCTGGA	55892
rs202063012	snp	C/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783364	CTAAAGTACAATATA[C/G]AGAGATTTTAATTTA	55892
rs202141048	snp	A/G	0.000568586	0.0168514	intron-variant	ACTRT3	GRCh38.p7	3:169769313	AGCCTGCTGGGAGAA[A/G]GAGGTACCTGATGAA	55892
rs202145739	snp	A/G	1.69916e-05	0.00291471	intron-variant	MYNN	GRCh38.p7	3:169784600	AAAATATTGAAATTT[A/G]AACTTCTAATTTGTT	55892
rs202149737	snp	C/T	1.64868e-05	0.00287109	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786539	TGACTTTACCATTAG[C/T]TCTTCCACTTGGGAC	55892
rs202207013	snp	C/T	1.73393e-05	0.00294437	missense	ACTRT3	GRCh38.p7	3:169769421	TGGCGCGGCCGATAA[C/T]GTTCGGGTAGATAAA	55892
rs367646476	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169785052	ACTCAGGGTTTACTA[C/T]GGTTATTATGAAAAA	55892
rs367907819	in-del	-/T			intron-variant	MYNN	GRCh38.p7	3:169785082	AAAAGGGGGGGGGGG[-/T]GGTGTTATCATGAAC	55892
rs367946936	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169780703	TATAAATGTGATGTA[A/T]GCAACTTACAGTTTG	55892
rs368002667	snp	A/G	4.94189e-05	0.00497062	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774329	TGTGAGCACCTTTTA[A/G]AGAGACTGAACAAAC	55892
rs368064836	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169783941	TTTAATTTTGACATG[C/T]TTATTGTAAAAAGTA	55892
rs368204978	snp	A/G	0.000330104	0.012843	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779492	GGAGTCAAACCTTAC[A/G]TCTGCCACTTATGTG	55892
rs368222098	snp	A/G	1.64836e-05	0.0028708	missense	ACTRT3	GRCh38.p7	3:169767707	TCAGGCCTGTATCAC[A/G]TTTCATTATGCTGCT	55892
rs368307673	snp	A/C			intron-variant	MYNN	GRCh38.p7	3:169775898	AGGGTGCTCATTAAT[A/C]CTTTTGACGAGGAAA	55892
rs368448793	snp	C/G	0.000153988	0.00877328	missense	ACTRT3	GRCh38.p7	3:169768117	AGGCCAGTAGTGAAG[C/G]CAGCAGCAAAGAGAG	55892
rs368467500	snp	A/G	0.000153988	0.00877327	missense, intron-variant, nc-transcript-variant	MYNN	GRCh38.p7	3:169784649	TTATCTGCGAATTAT[A/G]TGGAAATTCTTACAC	55892
rs368733155	snp	A/T	1.66546e-05	0.00288566	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774551	TACACAGGAACTTTA[A/T]ATCTTGACAGGTAAA	55892
rs368734042	snp	C/G			intron-variant	MYNN	GRCh38.p7	3:169782667	GACAGGGAGAGACTG[C/G]TTAAAATAAAGTTAT	55892
rs368752059	in-del	-/AG			intron-variant	ACTRT3	GRCh38.p7	3:169768553	TTTTTTTGGAGACAG[-/AG]TCTCGCTCTGTCACC	55892
rs368939302	snp	G/T			intron-variant	MYNN	GRCh38.p7	3:169774928	ACTGCAACCTCTGCC[G/T]CCCGGGTTCAAGCGA	55892
rs368939672	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169778531	AATTTTTCTGCAGTG[A/G]TTCACTGTCAGCTGT	55892
rs369171417	snp	A/G	1.64814e-05	0.00287061	missense	ACTRT3	GRCh38.p7	3:169767769	AGGTTCATATGACAC[A/G]GAGAGAAGAGGGCCT	55892
rs369262799	snp	A/G	1.64904e-05	0.00287139	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169786480	ACAGGATTCCATACA[A/G]AAAAGTCCTTTATCA	55892
rs369374351	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169777061	TGTTATCTGTTTGGC[A/G]GTTTATTTTATGGAG	55892
rs369406761	snp	A/G			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787939	ATTTTTATAGTGCCA[A/G]TCAAACAGCATGGTG	55892
rs369446786	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant, intron-variant	MYNN	GRCh38.p7	3:169783548	CTCAACAAACACTTT[C/G]GGTCCCATACAGGTC	55892
rs369545827	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169775458	TCTTCTGACACAGGA[A/G]GATTATAGGCTTTGG	55892
rs369585629	snp	C/T			upstream-variant-2KB	MYNN	GRCh38.p7	3:169771921	TCTGAGCAGCTCAAC[C/T]TGCGGAAAGGATGTG	55892
rs369643173	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169780121	GGAGTACAGTGGTGC[A/G]ATCTCGGCTCACTGC	55892
rs369701558	snp	A/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772682	TCACTTGGTTTTTCG[A/T]CTGAAGTGGCTGTAA	55892
rs369704984	snp	A/G	1.75946e-05	0.00296598	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769524	GCAGTGGTTCATGCC[A/G]CCGCTGCTGCCGCCG	55892
rs369876555	snp	C/T	1.651e-05	0.0028731	synonymous-codon	ACTRT3	GRCh38.p7	3:169768194	CTCAAAAAACATTTC[C/T]GTGATCTGTTGCCGG	55892
rs369877049	snp	C/G	5.01685e-05	0.00500817	missense, nc-transcript-variant, intron-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169778823	AAAGTGGAAGAGGTG[C/G]TCACTAAATGCAAAA	55892
rs369953876	snp	A/G	6.5912e-05	0.00574035	missense	ACTRT3	GRCh38.p7	3:169767953	TGTCTGAAGCACTGA[A/G]CAACATGATACCATG	55892
rs369979303	snp	G/T			intron-variant	MYNN	GRCh38.p7	3:169778542	AGTGGTTCACTGTCA[G/T]CTGTGAATAGCCATT	55892
rs370156352	snp	A/T	0.00199481	0.0315187	intron-variant	MYNN	GRCh38.p7	3:169776936	TGAACTCCTGACCTC[A/T]GGTGATGCGCCCACC	55892
rs370359272	snp	G/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788439	TGTGATAGGAATGTA[G/T]TGGAATGTGAAGAAA	55892
rs370473384	snp	A/G			intron-variant	ACTRT3	GRCh38.p7	3:169769083	CCTTGGAGATTTGTG[A/G]CCCGTGCGTTTGTAG	55892
rs370494498	snp	A/G	4.9476e-05	0.00497348	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779280	CAGTGAAACGGAAAC[A/G]TGGAAAATCACAGCC	55892
rs370635725	in-del	-/AAT			intron-variant	MYNN	GRCh38.p7	3:169784530	TTTAAACACTATAAT[-/AAT]TTTTGCCTTGTGTTC	55892
rs370659143	snp	C/T	1.71396e-05	0.00292737	intron-variant	MYNN	GRCh38.p7	3:169774589	TTTTATTTTCAGTTA[C/T]AAAAGCTAGTCAGTA	55892
rs370707485	snp	A/G			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787151	TAAAAATAAAATTTC[A/G]TATTTTCGCTCGTAA	55892
rs370732757	snp	A/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169779515	CTTATGTGGAAAGGC[A/T]TTTACCCAATGTAAC	55892
rs370800928	snp	C/T	0.00159617	0.0282053	intron-variant	ACTRT3	GRCh38.p7	3:169768618	CTGCAAGCTCCGCCT[C/T]CCGGGTTCACGCCAT	55892
rs370838629	snp	A/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773334	ACCTCCCGCACTGCC[A/T]CGGGAAGACAGAGCC	55892
rs370919663	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169777031	CTTATATTGGTCTTA[A/G]AGGCTACCTGACCTT	55892
rs371055233	snp	A/C	3.38238e-05	0.00411227	intron-variant	MYNN	GRCh38.p7	3:169784606	TTGAAATTTAAACTT[A/C]TAATTTGTTTTTCAG	55892
rs371285454	in-del	-/TTGT	0.00163834	0.0285742	intron-variant	MYNN	GRCh38.p7	3:169784732	TTGTGTTTTGTTTGC[-/TTGT]TTGTTTGTTTTAATT	55892
rs371339555	snp	G/T			intron-variant	MYNN	GRCh38.p7	3:169777137	CCCAAAAGACAATTT[G/T]TAGAAAGCTGTTGTG	55892
rs371357194	snp	C/T	0.000131807	0.00811701	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169782498	GCCATATGTCTGTGA[C/T]AGGTGTGGACAGAGA	55892
rs371392440	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789460	CAGTTCCCAGGGCAT[A/G]TATATGCTGGGGAAG	55892
rs371549875	snp	A/G	3.43519e-05	0.00414424	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786706	TATGGAATTGCTAAG[A/G]TATCATTGGTAGCAA	55892
rs371764107	snp	C/T	0.000153988	0.00877328	missense	ACTRT3	GRCh38.p7	3:169767729	TATGCTGCTGAAGCA[C/T]ATCTTATCAATGCCA	55892
rs371797431	snp	A/T			downstream-variant-500B	MYNN	GRCh38.p7	3:169789907	TTTTTTTTTCTTATT[A/T]TTATTATACTTTAAG	55892
rs371838865	snp	A/C	0.000153988	0.00877328	missense	ACTRT3	GRCh38.p7	3:169767773	TCATATGACACGGAG[A/C]GAAGAGGGCCTCTGG	55892
rs371898302	snp	C/T	4.94197e-05	0.00497066	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774419	GCTCATAGGAATGTG[C/T]TGGCCTCCTTTAGTG	55892
rs371919583	snp	A/T	1.8892e-05	0.00307338	intron-variant	MYNN	GRCh38.p7	3:169780796	AGTCTTTTAATCACC[A/T]TAGTCTTATGAATAG	55892
rs371926281	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773270	GGAGTGGGTCTCTGT[A/G]GTACATCCTGTACCG	55892
rs372166751	snp	A/T	0.000199887	0.00999517	intron-variant	MYNN	GRCh38.p7	3:169782669	CAGGGAGAGACTGCT[A/T]AAAATAAAGTTATAA	55892
rs372229879	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169776829	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGAATTAC	55892
rs372430905	snp	A/C/G/T	0.00398564	0.0444627	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772274	GCCTAACACGCGAAA[A/C/G/T]GTCCCCGGTTCGAAA	55892
rs372726113	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779031	TAGCGAAAAAGTCAT[C/T]TCAAACGAAAAAGAA	55892
rs372880819	snp	A/G			utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769711	CACCGTGCTCCTCAT[A/G]TTACCGCCCGCTATT	55892
rs372939031	snp	C/G/T	3.30142e-05	0.00406276	missense	ACTRT3	GRCh38.p7	3:169768148	CCAGCACAGCCTGGA[C/G/T]GGACATATAGAAGGC	55892
rs373002131	snp	C/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788838	AAGATACTATCCCTT[C/T]TTTGGCATTCTTCTC	55892
rs373064805	snp	A/G	1.65375e-05	0.0028755	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786440	AAACTCTAGACTCCA[A/G]TGCAGAGGATCATAC	55892
rs373083056	snp	A/G	3.30038e-05	0.00406212	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786568	ACTGAGGACCATCAC[A/G]TGCTTCTGCCTGTCA	55892
rs373100307	snp	C/T			missense	ACTRT3	GRCh38.p7	3:169767910	GCCACATAACAAAAG[C/T]TCTCCTTGATGTCTT	55892
rs373104233	snp	A/G/T	3.30214e-05	0.00406323	synonymous-codon	ACTRT3	GRCh38.p7	3:169768197	AAAAAACATTTCCGT[A/G/T]ATCTGTTGCCGGTTG	55892
rs373127460	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant, intron-variant	MYNN	GRCh38.p7	3:169783488	CTAGGTGAAAAACCA[C/T]ACATATGTGGTATTT	55892
rs373245655	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772790	CGCATGCCCACTGTG[C/G]CCAGCTGCTCCGCTT	55892
rs373374301	snp	C/T	0.00398564	0.0444627	intron-variant	ACTRT3	GRCh38.p7	3:169768601	GGCGCGATCTCAGCT[C/T]ACTGCAAGCTCCGCC	55892
rs373544656	snp	A/C	0.00107092	0.0231152	missense	ACTRT3	GRCh38.p7	3:169769411	CTCTGGCCCTTGGCG[A/C]GGCCGATAATGTTCG	55892
rs373552765	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789337	AGTTGAAATAATGTA[C/T]ATGTACTAGTTTTTT	55892
rs373559453	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169780151	CAAGCTCCGCCTCCC[A/G]GGTTCAAGCCATTCT	55892
rs373635558	snp	C/T	0.000157988	0.00888644	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769564	TCTGAGCCGCTCTAG[C/T]TACGGGCTCGGCCGG	55892
rs373647274	snp	G/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779308	GCCAAACTGTGCTCT[G/T]AAAGAACACTCTATG	55892
rs373821675	snp	A/C	3.303e-05	0.00406373	missense	ACTRT3	GRCh38.p7	3:169768099	GCACCTGAATTCAGC[A/C]CAAGGCCAGTAGTGA	55892
rs373897000	in-del	-/AAAT			intron-variant	MYNN	GRCh38.p7	3:169782842	AATACAAGGTGGGTG[-/AAAT]AAATTATATAACTTA	55892
rs373920039	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773358	CAGAGCCGGACGTGA[C/T]GCCACCGTGGAAGGA	55892
rs373956998	snp	A/C	0.0178098	0.0926698	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772304	ACCGGGCGGAAACAC[A/C]CTAAAAAATCCCTTT	55892
rs374143807	snp	A/G	6.68237e-05	0.00577991	missense, intron-variant, nc-transcript-variant	MYNN	GRCh38.p7	3:169784642	AGACCATTTATCTGC[A/G]AATTATGTGGAAATT	55892
rs374242920	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169782399	ATCTATAAAAAACTT[C/T]ATGAATTCTTGCTAT	55892
rs374434651	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169776945	GACCTCAGGTGATGC[A/G]CCCACCTTGGCCTTA	55892
rs374511289	snp	C/G	0.000146009	0.00854303	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769568	AGCCGCTCTAGCTAC[C/G]GGCTCGGCCGGGGCC	55892
rs374647065	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169774814	CTGTGATTTCACTTA[C/T]GTAAACTTGAACATT	55892
rs374675135	snp	C/T			intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774205	TCCTCTGTCCCTTCC[C/T]TCACTGAACGTTGAT	55892
rs374715098	snp	A/C	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169784928	AAAAAAAAAAAAAAA[A/C]AACTTGAAACATTTC	55892
rs374720312	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169778427	TGCTATCTGAAGAAG[C/T]CTCAGGATGAATGGA	55892
rs374761819	snp	A/G	0.0119091	0.0762411	intron-variant	ACTRT3	GRCh38.p7	3:169769308	CCAGCAGCCTGCTGG[A/G]AGAAGGAGGTACCTG	55892
rs374794441	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169784880	TTTTGCAGAAACATT[C/T]ACTCTGGATTTTTCA	55892
rs374921080	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169782524	AGAGATTTGCTCAAG[C/G]CAGCACACTGACCTA	55892
rs374941758	snp	A/C	0.000153988	0.00877328	synonymous-codon	ACTRT3	GRCh38.p7	3:169768050	ATGAGGCAGACAGTA[A/C]CCCTCAAAGATGGGC	55892
rs375000258	snp	G/T			intron-variant	MYNN	GRCh38.p7	3:169781335	CAGTTCTGTGTGTGT[G/T]AAATTTGAGATGACT	55892
rs375193685	snp	A/G/T	0.000132694	0.00814448	intron-variant	MYNN	GRCh38.p7	3:169783454	ATAGTACACCACTTC[A/G/T]CTATCTTTTATTTTC	55892
rs375219951	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169775170	TTAACCTACCAGTAC[C/T]AATACTGAAGTAAGG	55892
rs375360988	snp	C/G	1.67022e-05	0.00288978	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779546	CAGCTGAAAACGCAT[C/G]TAAGAACTCATACAG	55892
rs375604010	in-del	-/AAT	0.00358779	0.0422022	intron-variant	MYNN	GRCh38.p7	3:169777449	ATATTTAGGGAAAAA[-/AAT]CAAGTAGGAAGATTA	55892
rs375743196	snp	A/C	1.65261e-05	0.0028745	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779082	CGAAAACAGGGCAGA[A/C]TAAAACAGTGCAATA	55892
rs375918746	snp	C/G			intron-variant	MYNN	GRCh38.p7	3:169786142	CAGTATATGAAAATT[C/G]ACAAATGTGTGATTA	55892
rs376081050	snp	A/G	0.000247731	0.0111267	synonymous-codon	ACTRT3	GRCh38.p7	3:169768221	CCGGTTGGCCAGTGG[A/G]TTCAGCGCTGGCTCA	55892
rs376301222	snp	C/T			intron-variant	ACTRT3	GRCh38.p7	3:169768613	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	55892
rs376405392	snp	C/G			intron-variant	MYNN	GRCh38.p7	3:169777194	ACAGGTGGCACTTGA[C/G]GCAAAGCAAGTTTAA	55892
rs376453495	snp	C/G	6.86731e-05	0.00585934	missense	ACTRT3	GRCh38.p7	3:169769502	TGTCGATCACCACCG[C/G]TAGCTGGCAGTGGTT	55892
rs376484684	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772399	TGTTTGTTTTGTTTT[G/T]TTTTCTGAGGGAAGC	55892
rs376620710	snp	C/T	8.25375e-05	0.00642355	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774508	TCAGGTGAAGGCTGA[C/T]GGATTTCAGAAACTG	55892
rs376794081	snp	C/T	3.30153e-05	0.00406283	missense	ACTRT3	GRCh38.p7	3:169768156	GCCTGGATGGACATA[C/T]AGAAGGCAGGAACAC	55892
rs376816949	snp	A/G	5.38914e-05	0.00519065	intron-variant	MYNN	GRCh38.p7	3:169778750	AGAATATTGTCATGT[A/G]GCCTTGTTTCCTTGC	55892
rs376949029	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169781708	GGTCAATTGTAAAAT[C/T]CTGTGATAGGGAGAT	55892
rs376969984	snp	A/G	0.00716266	0.059414	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789118	GCCTACTGTATGTTA[A/G]ATTTTAGACTATTTT	55892
rs377394948	snp	A/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781363	ACTTAACACTTCTGA[A/T]TAGAGGTGTGCAATA	55892
rs377574590	snp	C/T	0.00019786	0.00994438	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779315	TGTGCTCTGAAAGAA[C/T]ACTCTATGTCTAATA	55892
rs377681054	in-del	-/AT	0.00557542	0.0525036	intron-variant	MYNN	GRCh38.p7	3:169778322	CAAAGTTTGGGAAAC[-/AT]AATTAAAGTCCCTCA	55892
rs377709436	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169783186	GAATAGAAATGTGGG[C/T]TTATGAATTGACATG	55892
rs397708676	in-del	-/T			intron-variant	ACTRT3	GRCh38.p7	3:169768544	TTTTTTTTTTTTTTT[-/T]GGAGACAGAGTCTCG	55892
rs397874977	in-del	-/A			intron-variant	MYNN	GRCh38.p7	3:169784930	AAAAAAAAAAAAAAA[-/A]CTTGAAACATTTCCT	55892
rs397877370	in-del	-/A			intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774229	GTTGATGAGAACTTA[-/A]CGGTTACTGATTTAC	55892
rs527388777	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775201	TCAGAGATGCTAGAA[C/T]GATTCTCTAAGATGC	55892
rs527457915	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780183	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	55892
rs527592742	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169776765	CTGGAGTGCAATGGC[A/G]TGATCTCGGCTCACT	55892
rs527873862	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773797	GCCGGGCGCATTCCC[A/G]GCTTTCTGGGCAGCC	55892
rs527939422	snp	C/T	1.7098e-05	0.00292381	intron-variant	MYNN	GRCh38.p7	3:169774586	ACATTTTATTTTCAG[C/T]TATAAAAGCTAGTCA	55892
rs528008563	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781789	CTTGACAAAAGTATC[A/G]TTAGTAGAGGCCAGT	55892
rs528011487	snp	A/G	0.0146672	0.084371	intron-variant	MYNN	GRCh38.p7	3:169775223	CTAAGATGCTTACTG[A/G]TGTCACTGCATTAAC	55892
rs528076172	snp	A/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169779686	TCTATTCATCAAAGT[A/T]TTTAACAGTGTTAAA	55892
rs528123194	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169780311	GATCCGCCCGCCTCC[A/G]CCTTCCAAAGTGCTG	55892
rs528131349	snp	C/T	0.00721	0.0596072	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787975	CTTTTTCTTTTTTTT[C/T]CCCCCCACAAGGCTG	55892
rs528213512	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788694	TGATACGATTGAAGT[A/G]GCTAAGATTGATTGA	55892
rs528377466	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772991	GCAGCAGTTTCCACC[A/G]GTGGGGCCCCGAGGA	55892
rs528412350	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169785446	TACAACCTGGTGTGC[A/G]AGACCAGAAACCTAA	55892
rs528546344	snp	A/C			intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773883	GAGCAGTTTTTAAAA[A/C]CTCGTACTGTTCTGC	55892
rs528604912	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772081	GAAATGGTTTCAGCT[C/G]TGTTCAATTGGGCAT	55892
rs529069937	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786903	ATGAATTATGTAGCA[C/G]TATTTTGGGTGGATG	55892
rs529082999	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777199	TGGCACTTGAGGCAA[A/G]GCAAGTTTAATTAGA	55892
rs529150453	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169777966	TGTGCTGGTGGCTCA[C/T]GCTTGTAATCCTAGC	55892
rs529234164	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783661	ATATGGTATTTAGTC[A/G]TACTGTACCTATAGC	55892
rs529287358	snp	A/T	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169784515	CAATTTGAAACCAAA[A/T]TTAAACACTATAATA	55892
rs529295246	snp	C/G/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775407	GTCTTATTTCTGTCT[C/G/T]TCTTATGAAAGTGAA	55892
rs529684573	snp	C/T			intron-variant	ACTRT3	GRCh38.p7	3:169769086	TGGAGATTTGTGGCC[C/T]GTGCGTTTGTAGTAA	55892
rs529819424	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773603	CCGGGGTGGCCTGGG[C/T]CACAACCTCTGCTGT	55892
rs530098316	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780883	GTTAACACGTTCAAG[A/G]AACCACAAGGAAGCC	55892
rs530118157	snp	A/G	0.000103235	0.00718378	intron-variant	MYNN	GRCh38.p7	3:169784588	CTAGCAGCTTTTAAA[A/G]TATTGAAATTTAAAC	55892
rs530294731	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780538	AATCTTATATGACTT[A/G]TGCAACCAAAACACT	55892
rs530357984	snp	A/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781556	AGACGGCCCTGAGGC[A/T]CTCTAACTTTATGAG	55892
rs530699693	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772305	CCGGGCGGAAACACA[C/G]TAAAAAATCCCTTTT	55892
rs530715265	snp	C/T	1.66576e-05	0.00288592	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779541	GTAACCAGCTGAAAA[C/T]GCATGTAAGAACTCA	55892
rs530720725	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772258	AGTGGTTATCACGTT[A/C]GCCTAACACGCGAAA	55892
rs530776043	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771366	TAATAAATATAAAAA[A/T]TTATGTTTATATATA	55892
rs530894442	snp	G/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777829	GCTAATTTGGGTTGA[G/T]TATCACCAAAAAAGG	55892
rs530909102	snp	A/T	0.00159617	0.0282053	intron-variant	MYNN	GRCh38.p7	3:169777085	TATGGAGCACTAAAC[A/T]CAATTAGAGACCAAA	55892
rs530962048	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169771983	AAAAAAGGCCACCCA[A/G]AGGAAGGGCAACTCG	55892
rs531068882	snp	A/G	0.00159617	0.0282053	intron-variant	MYNN	GRCh38.p7	3:169777980	ACGCTTGTAATCCTA[A/G]CACTTTGGGAGCCCA	55892
rs531096955	in-del	-/CA			downstream-variant-500B	MYNN	GRCh38.p7	3:169789947	CATGTGCACAGCATG[-/CA]CAGGTTTGTTACATA	55892
rs531197853	in-del	-/AAG	0.000811292	0.0201243	cds-indel, nc-transcript-variant	MYNN	GRCh38.p7	3:169779042	TCATCTCAAACGAAA[-/AAG]AAGAAGAAGGCTTTC	55892
rs531415435	in-del	-/CT			intron-variant	MYNN	GRCh38.p7	3:169775743	GCCCACTGATAACCC[-/CT]GTTAACCTTTTGATA	55892
rs531509080	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169784943	AAACTTGAAACATTT[C/T]CTCCTTTGAAAACCT	55892
rs531579106	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169785783	CCAAAATCATGTCAA[C/T]ACTTTAGAGTAACGG	55892
rs531838273	snp	A/C/T	0.0002372	0.0108879	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769571	CGCTCTAGCTACGGG[A/C/T]TCGGCCGGGGCCGAG	55892
rs531978060	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781452	TTGGCAATCATTAGC[A/G]TTTGGCAGTCATCAG	55892
rs532033201	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169774734	AGGATGAGCAGGCAA[C/T]ATTTTTCATAAGCAC	55892
rs532038399	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773446	AGAAACTGTGTTCCC[C/T]CCTTGGGTTGCTATC	55892
rs532074762	snp	C/T	0.0023933	0.0345097	intron-variant	ACTRT3	GRCh38.p7	3:169768504	AGTGTCAGCCAAAAA[C/T]AGCACAGCTACTTAC	55892
rs532098077	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169773010	GGGCCCCGAGGAAGG[A/G]GAGGATGATGGGAGA	55892
rs532528583	snp	A/C/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169782942	TATAAAAACCTTTTC[A/C/G]GCTTCCTAAAGGGTC	55892
rs532731282	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788891	CATAATATGCATATA[C/T]TTAGTTGTATCTGGT	55892
rs533077847	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787815	TGAATGTAGAAAATT[C/T]GTTATTATCCTGATA	55892
rs533098931	snp	C/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169778077	CTACAAAAAAAATAG[C/G]CAGGCATGGTAGCAC	55892
rs533117102	snp	G/T			intron-variant	MYNN	GRCh38.p7	3:169783805	AGATAATCAATAGTT[G/T]TTAAATGATTTGGAT	55892
rs533201408	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770005	GGCAGTGTCTGCTTC[C/T]GAAATGTTAAACTTC	55892
rs533208755	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772246	TTTCCGTAGTGTAGT[G/T]GTTATCACGTTCGCC	55892
rs533286429	snp	C/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169784785	ATTCCTTAAAATGCT[C/G]AGATGAGATTTACAT	55892
rs533457564	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771139	TTTATATTTATATAT[A/C]ATAAATATATAAAAA	55892
rs533705179	snp	C/T			missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169778934	CAACAGACTTGTCTT[C/T]TTACTCTGCGAGATT	55892
rs534183708	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780844	CAGGACAGTAGAATT[A/G]TAATTGTGGTTCCAC	55892
rs534194279	snp	C/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780092	AGACAGAGTCTCACT[C/G]TGTCGCCCAGGCTGG	55892
rs534301327	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772264	TATCACGTTCGCCTA[A/C]CACGCGAAAGGTCCC	55892
rs534336295	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789129	GTTAGATTTTAGACT[A/G]TTTTAAAAGAAACCG	55892
rs534383623	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775845	CCTTTTATATTGTAA[C/T]TTATCATGGAAATAT	55892
rs534520515	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773069	AGTGCGCAGCTGGCT[C/T]CAGGAGAGAGGCCCG	55892
rs534605032	in-del	-/ATTTT	0.000963831	0.0219314	intron-variant	MYNN	GRCh38.p7	3:169774573	ACAGGTAAAGTACAC[-/ATTTT]ATTTTCAGTTATAAA	55892
rs534797107	snp	C/T			intron-variant	ACTRT3	GRCh38.p7	3:169768792	CTCGGCCTCCCAAAG[C/T]GCTAGGATTACAGGC	55892
rs534843911	in-del	-/AT	0.00318978	0.0398085	intron-variant	MYNN	GRCh38.p7	3:169782788	TTATGATTTTTGCAC[-/AT]ATTTGTTAAATATAA	55892
rs534942131	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169785632	GAGAGGATTCATTCC[A/G]GGCAGAGAACACTGT	55892
rs535038917	snp	A/G	0.00176249	0.0296334	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786521	ATGTGAAGCCTTCTG[A/G]TATGACTTTACCATT	55892
rs535116277	snp	C/T	1.68026e-05	0.00289845	intron-variant	MYNN	GRCh38.p7	3:169786408	ATTTTTTTTTCCTTC[C/T]ATTCTAGGTGCAGAT	55892
rs535118005	in-del	-/ATTA			intron-variant	MYNN	GRCh38.p7	3:169785342	AAACTGCAGTAAGTC[-/ATTA]ATTTAACCACTTGTT	55892
rs535266335	in-del	-/TA	0.449473	0.150701	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771429	AAATATATAAAAATT[-/TA]TGTTTATATATAATA	55892
rs535361279	in-del	-/A	0.123452	0.215605	intron-variant	MYNN	GRCh38.p7	3:169778487	GTGTTCTAGGGTTTT[-/A]AAAAAAAAAGCCAGA	55892
rs535441416	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169774793	GTTTATTTACTGAAA[C/T]AAAGCCTGTGATTTC	55892
rs535518592	snp	A/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169782269	AAACTTTTTGAACTG[A/T]TCTCAGAACTAATGT	55892
rs535577373	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169782944	TAAAAACCTTTTCAG[C/T]TTCCTAAAGGGTCAT	55892
rs535627393	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770241	TATAAAATATTAAAA[A/T]ATATATAAATTTATA	55892
rs535767728	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169776481	TAATAGATTTCATAG[A/G]CATGTCCTGAGGATA	55892
rs535962523	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169781057	GTAAACAGGAATCTA[C/T]AGATAAAACCCAAGC	55892
rs536622454	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771739	GTGTCTGATTCTGCA[C/T]ACATCTGTAGAGAAT	55892
rs536710992	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169785849	AAGTACATCTTTAGT[C/T]AGTGTGCTGATTGCT	55892
rs536765699	snp	A/C	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777394	TCTGGCTTATACTTA[A/C]AACAGAGAGGGAAAG	55892
rs536775907	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169782274	TTTTGAACTGATCTC[A/G]GAACTAATGTTTTGA	55892
rs536887748	snp	C/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788687	TATTATTTGATACGA[C/T]TGAAGTGGCTAAGAT	55892
rs536888184	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169773055	AAGCCCCCGCACGCA[C/G]TGCGCAGCTGGCTTC	55892
rs536906238	snp	A/G	4.95135e-05	0.00497537	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779207	GATAATTCAGAACTC[A/G]AGTTGACATCAGTTG	55892
rs536906277	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169789019	TATTACATATTTTTA[C/T]GGAAGTCTTTAGAAG	55892
rs536918510	in-del	-/A	0.00199481	0.0315187	intron-variant	MYNN	GRCh38.p7	3:169781828	AATGGAAGTAGATAG[-/A]ACACTTGGAGTCTCA	55892
rs537090759	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772189	AATTGCGAATTGACA[C/T]TTACATATCAAGGAC	55892
rs537624225	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775518	CTCCTTGAGCATGAT[A/G]CAATCTCTCTGGGCC	55892
rs537689232	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769691	GCGGAAGGACTCGCT[A/G]GACGCACCGTGCTCC	55892
rs537737767	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169782094	CATATGAATTTTTCT[C/T]AGTGAAATAGGAAGC	55892
rs537829908	snp	C/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169782170	TTTGAGGAGAGAGTT[C/G]ACAAGTCAAAGAGTG	55892
rs538087452	snp	C/T	0.0023933	0.0345097	intron-variant	MYNN	GRCh38.p7	3:169776365	GGCTCAGGGGCCAGA[C/T]TACCTTGGTCAAATC	55892
rs538090121	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783323	TAATTACTAATATTC[A/G]TTTACTTGGATCACT	55892
rs538151497	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783958	TATTGTAAAAAGTAG[C/T]TTGTAAATTGTATAA	55892
rs538302984	in-del	-/TTT			upstream-variant-2KB, cds-indel	MYNN	GRCh38.p7	3:169772335	TTTTTTTTTTTTTTT[-/TTT]CCTTCGCTTGGAAGA	55892
rs538350012	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780910	AGCCACAGTGGTTGA[C/T]AGGAAATAAGCAGGG	55892
rs538357832	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772335	TTTTTTTTTTTTTTT[A/T]TTCCTTCGCTTGGAA	55892
rs538398544	snp	A/C	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768924	TTATAGTATAGTTTA[A/C]ATGTCAATTGAAGAG	55892
rs538713784	snp	C/T	0.00199481	0.0315187	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769836	CCCTTCACAAGTGCA[C/T]TTCTCAAATACCCAG	55892
rs539029828	snp	A/G	0.0130921	0.0798413	downstream-variant-500B	MYNN	GRCh38.p7	3:169789849	ATGATGCTCTTGAAT[A/G]TAATTTTCAATATTT	55892
rs539358984	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788071	TTAAACTACACCTGT[A/G]GTACAGTTAATATGT	55892
rs539398159	snp	A/C	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169786034	AAGAAGTATAACGAC[A/C]TTTACTCTCAAAGAA	55892
rs539459621	snp	G/T	0.00676609	0.0577691	intron-variant	MYNN	GRCh38.p7	3:169777323	TCAAATTTTAGTCCT[G/T]TAAAATAGTATCACC	55892
rs539508930	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169774932	CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT	55892
rs539849625	in-del	-/CCTGTCGCCTC	0.00318978	0.0398085	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772636	GTAAAAGTGGTTAGT[-/CCTGTCGCCTC]CTGAGCATTTTTGTA	55892
rs539880130	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783818	TTTTTAAATGATTTG[A/G]ATTAAATTGCACAGA	55892
rs540109161	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781344	GTGTGTTAAATTTGA[A/G]ATGACTTAACACTTC	55892
rs540349996	snp	C/G	3.30142e-05	0.00406276	missense	ACTRT3	GRCh38.p7	3:169768165	GACATATAGAAGGCA[C/G]GAACACCCAGATGCT	55892
rs540615245	snp	C/T			downstream-variant-500B	MYNN	GRCh38.p7	3:169789815	TTCCTGATGTTCTAC[C/T]TTTGGGAAGCAGTTT	55892
rs540629139	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772286	AAAGGTCCCCGGTTC[A/G]AAACCGGGCGGAAAC	55892
rs540744948	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772236	CAAAGTGGGGTTTCC[A/G]TAGTGTAGTGGTTAT	55892
rs540856834	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169783288	GTTTTAATATATGAA[A/G]ACTTATGAACAGTAT	55892
rs541193206	snp	A/T	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169778695	TTTAAAATACATTGA[A/T]GTATATATGCAGCTC	55892
rs541225434	snp	G/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169777481	ATTTGAGGGTAAGGG[G/T]TGTGTGTGTGTGTGT	55892
rs541682001	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169785511	ATGTAGGGCATAATC[A/G]ACACAAAAGTGCTAA	55892
rs541719890	snp	A/G	1.99698e-05	0.00315983	missense	ACTRT3	GRCh38.p7	3:169769363	TGAGCTTGGTCGCCC[A/G]CGCAGAGTTCTAGCC	55892
rs541845903	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169775093	TCCAGTTTCCCATTG[C/T]TTTTTGGTCCTTGAA	55892
rs541879512	snp	A/G	0.00279162	0.0372561	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773219	AGCTCTCGTATCCAT[A/G]ACGCCTGCTGCTTCG	55892
rs541917451	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169782717	CTTGGGCCTTTTAGC[A/G]AAGTAGATCGGAAAC	55892
rs542089926	snp	A/C			intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774004	CAACAGATGTGAAAG[A/C]GTCAGGTTTTGCTGT	55892
rs542164822	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769726	GTTACCGCCCGCTAT[C/T]GCTTCTCGCAGGAAT	55892
rs542407881	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, intron-variant	MYNN	GRCh38.p7	3:169772886	GCACAAAAAAACCAG[A/G]GGGTGCCAAGAGTTT	55892
rs542834865	snp	G/T			upstream-variant-2KB	MYNN	GRCh38.p7	3:169772226	AAACCCTCTCCAAAG[G/T]GGGGTTTCCGTAGTG	55892
rs542973637	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772281	ACGCGAAAGGTCCCC[A/G]GTTCGAAACCGGGCG	55892
rs543066874	snp	C/T	0.00159617	0.0282053	intron-variant	MYNN	GRCh38.p7	3:169776828	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGAATTA	55892
rs543090619	snp	G/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789347	ATGTACATGTACTAG[G/T]TTTTTTAAGTATTCT	55892
rs543118756	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786748	AAGGTGCATATATTC[A/G]TATTAAATTCCCATT	55892
rs543179747	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777853	AAAAAGGTGGGAGGG[C/T]TGCTAGAGAGAGTTT	55892
rs543504313	snp	C/G	0.0146672	0.084371	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771886	GCTGAATAACGAAAG[C/G]CCCCTGCTTCGCCCC	55892
rs543651306	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775888	ATCTAGAATCAGGGT[A/G]CTCATTAATCCTTTT	55892
rs543662869	in-del	-/C	0.013139	0.0799804	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787975	TTTTTCTTTTTTTTT[-/C]CCCCCCACAAGGCTG	55892
rs543741166	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169784393	GATACATTTCTGTTT[A/G]TGAAAATGCTCAAGT	55892
rs544216439	snp	A/T	0.000136029	0.00824597	intron-variant	MYNN	GRCh38.p7	3:169782686	AAATAAAGTTATAAA[A/T]AAAAGAAAAAGGGGA	55892
rs544341383	snp	G/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789125	GTATGTTAGATTTTA[G/T]ACTATTTTAAAAGAA	55892
rs544351432	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781483	CATATGACAGTATTT[A/G]AAGCTGTAACCCTGG	55892
rs544374308	snp	A/C	0.000980152	0.0221159	intron-variant	ACTRT3	GRCh38.p7	3:169769295	ACCCTCCCCAGCCCC[A/C]GCAGCCTGCTGGGAG	55892
rs544397669	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772761	GGTATAAAGCCCACC[C/T]TCCTCTAATGTTGCG	55892
rs544650101	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772302	AAACCGGGCGGAAAC[A/G]CACTAAAAAATCCCT	55892
rs544928597	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788409	AGAATGTTACCTAAT[C/G]TCTTCTGGGTTAAAT	55892
rs545067742	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169776998	GCCTTGAACAATTAA[C/T]GTATGACTTCCTGCT	55892
rs545176834	snp	A/G	1.64885e-05	0.00287123	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779408	TCCAAGGCCAAGCCA[A/G]TGTGTAACACATGTG	55892
rs545196582	snp	A/C	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785722	AGAATACAGATAATT[A/C]CAATTTTACGAAAGC	55892
rs545395904	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169778580	ATCTCTTGAAGTTCT[A/G]TAAAATTGGAGATTT	55892
rs545408721	snp	A/G	3.35886e-05	0.00409795	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169786669	GATTTTTTTACAACA[A/G]TTATACTGACTTTGT	55892
rs545438143	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-5-prime, intron-variant	MYNN	GRCh38.p7	3:169772948	TCTCAGCTAAAAAAT[C/T]CCCTATGGCAGAGAT	55892
rs545530928	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169775220	TCTCTAAGATGCTTA[C/T]TGATGTCACTGCATT	55892
rs545842096	in-del	-/GAA			intron-variant	ACTRT3	GRCh38.p7	3:169768934	GTTTAAATGTCAATT[-/GAA]GAGAATAACCCAAGT	55892
rs545854486	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770513	ATATAAATATATAAA[A/C]ATTTATATTTATATA	55892
rs545897996	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775706	ATAGAAAAAACAAAA[A/G]AGAAACACCTGAAAT	55892
rs545900130	snp	G/T			intron-variant	MYNN	GRCh38.p7	3:169775269	AGGAATCTGATAATG[G/T]AGGCACTGTGTGTCT	55892
rs546074889	snp	C/T	1.672e-05	0.00289132	intron-variant	MYNN	GRCh38.p7	3:169783432	AATTGATAAATATTA[C/T]ATTGGTATAGTACAC	55892
rs546176906	snp	A/C	0.00358779	0.0422022	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772315	ACACACTAAAAAATC[A/C]CTTTTTTTTTTTTTT	55892
rs546408140	snp	C/T	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768426	GACCCTCAGTTAATT[C/T]CCCGCGTTTATTACC	55892
rs546441523	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169773004	CCGGTGGGGCCCCGA[A/G]GAAGGGGAGGATGAT	55892
rs546480611	in-del	-/TT	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169784561	TCATAAACATTGATA[-/TT]TTTGTCTTAGCTAGC	55892
rs547068926	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772098	GTTCAATTGGGCATA[C/G]GCTATTTTTCCTTTT	55892
rs547205100	in-del	-/A	0.00318978	0.0398085	intron-variant	MYNN	GRCh38.p7	3:169785431	GTACTCAAAGCACTT[-/A]ACAACCTGGTGTGCG	55892
rs547540503	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169783053	ATTCTGGGATTTTCA[A/G]ATAAGGTAATTCAGA	55892
rs547636306	snp	A/C	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169785921	AAAGTGCCATACATA[A/C]TGTTCTGAACTCACA	55892
rs547657087	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169776018	TATAATGAAATCTTC[A/G]AGTGAGTTCTTTATA	55892
rs547657187	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769595	GGCCGAGTGCCTGGA[A/G]CGCCGCGTCACAGAG	55892
rs547719947	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169769947	CGCCCTTGAAACTGG[A/G]GAAAAATGAGACTTA	55892
rs547740087	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777202	CACTTGAGGCAAAGC[A/G]AGTTTAATTAGAAGA	55892
rs548030117	snp	C/G			intron-variant	MYNN	GRCh38.p7	3:169775941	AGAAGTATCCAGTGG[C/G]GGGAGGGGAGGGAGA	55892
rs548712273	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787973	TTCTTTTTCTTTTTT[C/T]TTCCCCCCACAAGGC	55892
rs548811356	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169773057	GCCCCCGCACGCAGT[A/G]CGCAGCTGGCTTCAG	55892
rs548833592	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169779650	GCACACACTACTTGT[A/G]ACCAGAATTTGGTAT	55892
rs548963432	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169784982	AACAGTCCCAAGCAT[A/G]AAGGAACATATAAGC	55892
rs549103995	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	MYNN	GRCh38.p7	3:169771985	AAAAGGCCACCCAAA[G/T]GAAGGGCAACTCGGG	55892
rs549233480	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772261	GGTTATCACGTTCGC[C/T]TAACACGCGAAAGGT	55892
rs549451864	snp	C/G			intron-variant	MYNN	GRCh38.p7	3:169781109	CAGGGTGGCAGCAGT[C/G]AAAGAAATAAGTAGT	55892
rs549488949	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771381	TTTATGTTTATATAT[A/C]ATAAATATATAAAAA	55892
rs550009271	snp	G/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169784390	GCAGATACATTTCTG[G/T]TTATGAAAATGCTCA	55892
rs550035022	snp	A/G	1.65029e-05	0.00287248	intron-variant	MYNN	GRCh38.p7	3:169783573	CAGGTCTGTGTTTAG[A/G]GAGAACGTATTATTT	55892
rs550144389	snp	C/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169785073	TTATGAAAAAAAAGG[C/G]GGGGGGGGTGGTGTT	55892
rs550177709	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169774770	ATAAACAGTAAGATT[C/T]CTGACACGTTTATTT	55892
rs550345678	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769574	TCTAGCTACGGGCTC[C/G]GCCGGGGCCGAGTGC	55892
rs550483059	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169775283	GTAGGCACTGTGTGT[C/T]TCCCCTGTATAACGA	55892
rs550621342	snp	C/T	0.0252325	0.109451	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772337	TTTTTTTTTTTTTTT[C/T]CCTTCGCTTGGAAGA	55892
rs550667087	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169780438	TTGATTCTACTGGTG[C/T]TTTCAGTGGTCTGGA	55892
rs550881630	snp	G/T			downstream-variant-500B	MYNN	GRCh38.p7	3:169790088	AGAAATACCATCAAG[G/T]AAAATTCTTTAAATT	55892
rs550963818	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787061	CCCTCATAATTTAAG[C/T]AAAATCCACGATAGT	55892
rs551108830	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169786163	TGTGTGATTAAGCCG[A/G]TATAACAGCTCACCC	55892
rs551164922	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169779997	ACAGTTACCTTTATT[C/T]TGCATGTCCTCTGCC	55892
rs551278211	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772253	AGTGTAGTGGTTATC[A/T]CGTTCGCCTAACACG	55892
rs551342926	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788898	TGCATATATTTAGTT[A/G]TATCTGGTATCATTC	55892
rs551354727	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770020	TGAAATGTTAAACTT[A/C]TAAAATAAGGAGAAA	55892
rs551551466	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775496	TCTTTCCTGTCAGTC[A/G]CTATGTCTCCTTGAG	55892
rs551617982	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169778126	ACTTGGGAAGCTGAC[A/G]CAGGAGCCCAGGAGT	55892
rs551695285	snp	A/G			synonymous-codon	ACTRT3	GRCh38.p7	3:169768128	GAAGCCAGCAGCAAA[A/G]AGAGCCAGCACAGCC	55892
rs551881387	snp	C/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169776150	GAATACACGGTAGAG[C/G]ACTTTTCTTTGAGAC	55892
rs552252674	snp	C/T	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768917	GTCCACATTATAGTA[C/T]AGTTTAAATGTCAAT	55892
rs552625234	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773815	TTTCTGGGCAGCCAC[C/G]TCTCGTTTTGGAGAA	55892
rs552639934	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169784504	GATTAAAGTGACAAT[C/T]TGAAACCAAATTTAA	55892
rs552675586	snp	A/C	0.00358779	0.0422022	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772266	TCACGTTCGCCTAAC[A/C]CGCGAAAGGTCCCCG	55892
rs552726017	snp	A/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169774622	CTTCACAGCAAAAGT[A/T]GATTTGTATTTTTTC	55892
rs552733256	snp	C/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787860	CCCCATGCCACTTTT[C/T]CCACATATTAATTTA	55892
rs552842907	in-del	-/GTAAGATTTCT	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169774761	CACAGATAATAAACA[-/GTAAGATTTCT]GTAAGATTTCTGACA	55892
rs552864955	snp	G/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169782813	AATATAAAAGCTGAC[G/T]TATTTTCTAGAATAA	55892
rs553428729	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787215	CTCTATTAATATATT[C/G]TTAGAAATAACTTTT	55892
rs553494041	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785147	ACAGGTAGCCCTACA[C/T]TGTTATAATATATAA	55892
rs553632957	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169782744	AAACTTTGTAGTTAG[A/G]TATCTGTTTATATTT	55892
rs553671956	snp	G/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777489	GTAAGGGGTGTGTGT[G/T]TGTGTGTGTGTGTTT	55892
rs553739043	snp	C/T	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768984	GTTAATATTCTTAAA[C/T]GAATTCGTTCGATAA	55892
rs553876005	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169774865	ATTTTATTTTTGAGA[C/T]GGGCTCACCGTCACC	55892
rs554002927	snp	A/G	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768432	CAGTTAATTCCCCGC[A/G]TTTATTACCAATATC	55892
rs554072545	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169776593	ACTTGTAAACAAAAG[C/T]AAATCTGTTATTGAA	55892
rs554072593	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769815	CATCAAAAGATTCAA[C/T]TCTAACCCTTCACAA	55892
rs554424488	snp	C/T	0.0130921	0.0798413	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786795	ATTATTTTTCATTCA[C/T]TGAAGTAAAAGCACC	55892
rs554675705	in-del	-/GA	0.00358779	0.0422022	intron-variant	MYNN	GRCh38.p7	3:169776022	ATGAAATCTTCAAGT[-/GA]GTTCTTTATAAGTTG	55892
rs554923763	snp	C/G			missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786559	CCACTTGGGACTGAG[C/G]ACCATCACATGCTTC	55892
rs554968649	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169789074	TTTCTAAATAAATTT[A/T]ATTTTCTTTTGTATT	55892
rs555088072	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169778202	GGCAACAGAAGAATA[C/T]CCCATCTCAAAACAG	55892
rs555267231	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772282	CGCGAAAGGTCCCCG[A/G]TTCGAAACCGGGCGG	55892
rs555285868	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780048	CTATTGGTACGTTTA[C/T]ATTCGTACTTTTTTC	55892
rs555499765	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785445	TTACAACCTGGTGTG[C/T]GAGACCAGAAACCTA	55892
rs555561656	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169786308	ACCGCTTGAGTAAAG[A/G]TATGGTGGTTGGAAT	55892
rs555578919	snp	C/T			intron-variant	ACTRT3	GRCh38.p7	3:169768877	TGTCCTTTGGAACCT[C/T]GTGACTTTTAAAAAA	55892
rs556170408	snp	C/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775020	ATTTTTGTATTTTTT[C/G]GTAGAGACAGGGTTT	55892
rs556214759	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783332	ATATTCATTTACTTG[A/G]ATCACTGAAAATACC	55892
rs556276089	snp	G/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786688	TACTGACTTTGTAAG[G/T]AATATGGAATTGCTA	55892
rs556289188	snp	A/C	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169782198	GTGACTAGACTCATG[A/C]AAATAATTGCCTGCA	55892
rs556479269	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169784138	GACTTTATATTCTGA[C/T]GCGCTTTAGTTTACA	55892
rs556507219	in-del	-/C			intron-variant	MYNN	GRCh38.p7	3:169777724	TATCTTAGTACCACA[-/C]CATGGTAGATGCTTA	55892
rs556546982	snp	G/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775524	GAGCATGATGCAATC[G/T]CTCTGGGCCTCAGTT	55892
rs556640841	snp	C/T			upstream-variant-2KB	MYNN	GRCh38.p7	3:169772217	GACTTTACAAAACCC[C/T]CTCCAAAGTGGGGTT	55892
rs556696467	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789543	CCAGGCTGGAGTGCA[A/G]TGACGTGATCTCAGC	55892
rs556950359	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169776852	GGAATTACAGGCACC[C/T]GCCATCATGCCCAGC	55892
rs557014287	snp	A/C			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788802	TTCTGCTCTTCTAGA[A/C]TGATGTGTAGAGAAA	55892
rs557416175	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787407	TATCTTGTCAAAGAC[A/G]GTTTCAAAATTTGAT	55892
rs557416860	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785292	CTGGTGTGTAAATAC[C/T]TAAACATCGTAAGTA	55892
rs557417257	snp	C/T	1.65083e-05	0.00287296	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779135	GCATCTGTTGAATTA[C/T]TCCTAGATGCAAATA	55892
rs557478326	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777330	TTAGTCCTTTAAAAT[A/G]GTATCACCAGCACTA	55892
rs557599347	in-del	-/GATT	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788700	GATTGAAGTGGCTAA[-/GATT]GATTGAGCTTTTCTT	55892
rs557619631	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169778587	GAAGTTCTGTAAAAT[C/T]GGAGATTTTTTACCT	55892
rs557674963	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788132	TAATTTTCTCTATTT[A/G]GGACCCAAGTCATAA	55892
rs557739889	snp	A/G	0	0	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771676	GTCATATGAAATTCA[A/G]GTTTGGAAAAATTTG	55892
rs557796518	snp	C/T	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169769130	GGGCTTTCCAGCTCC[C/T]GGCTTTCTTATTCTT	55892
rs557859584	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769658	GGGGGCGCAGGCAGG[A/G]GGTCGGCAGGGCCCC	55892
rs557880629	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169776766	TGGAGTGCAATGGCG[C/T]GATCTCGGCTCACTG	55892
rs558360108	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169781489	ACAGTATTTAAAGCT[A/G]TAACCCTGGCTAAGG	55892
rs558494994	in-del	-/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773962	TGTAACATAAGTATG[-/T]CTACTGAGCTTGAAA	55892
rs558760058	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789160	TAGATTATATAAAAA[A/T]TTTTTTGCTGTTTTT	55892
rs558996565	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772721	ATTAAAAATCTTCTG[C/G]TCCAGACGCAGGAAA	55892
rs559261872	snp	A/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773071	TGCGCAGCTGGCTTC[A/T]GGAGAGAGGCCCGCG	55892
rs559298897	snp	C/G	0.000399281	0.0141238	missense, nc-transcript-variant, intron-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169778811	GCTGACTATCTCAAA[C/G]TGGAAGAGGTGGTCA	55892
rs559501107	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785532	AAAGTGCTAAAGAAG[A/G]TACTATGTTTTTCTG	55892
rs559527088	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771772	GAAAACAAGCAGTCA[A/G]TTTAGAACTTCTGCT	55892
rs559598118	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169776951	AGGTGATGCGCCCAC[C/T]TTGGCCTTACAGGCA	55892
rs559663030	snp	A/G	0.00716266	0.059414	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771129	TATATAAAAATTTAT[A/G]TTTATATATCATAAA	55892
rs559772812	snp	C/T			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789477	ATATGCTGGGGAAGC[C/T]CCATAGGTGATTTTA	55892
rs560139882	snp	A/C			downstream-variant-500B	MYNN	GRCh38.p7	3:169789925	ATTATACTTTAAGTT[A/C]TAGGGTACATGTGCA	55892
rs560180684	snp	A/T			stop-gained	ACTRT3	GRCh38.p7	3:169768257	CAAGACTGGGCCATC[A/T]CACGGCTTCAGCTTT	55892
rs560199614	snp	C/T	0.00199481	0.0315187	intron-variant	MYNN	GRCh38.p7	3:169774907	GCAGTGGGGCAATCT[C/T]GGCTCACTGCAACCT	55892
rs560270111	snp	C/T	6.75835e-05	0.00581268	intron-variant	MYNN	GRCh38.p7	3:169774570	TTGACAGGTAAAGTA[C/T]ACATTTTATTTTCAG	55892
rs560333278	snp	A/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775133	TCTTCTGTCTCCCTC[A/T]TTCTGACTCCTGTTA	55892
rs560597911	snp	A/C	0.000399281	0.0141238	missense	ACTRT3	GRCh38.p7	3:169767783	CGGAGAGAAGAGGGC[A/C]TCTGGACAAGAAAAG	55892
rs560676896	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788642	CATTCTGCCTTTGCA[C/T]AGATTAGCCTTCAAA	55892
rs560750222	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773233	TGACGCCTGCTGCTT[C/T]GGGGGACCCCTGGCA	55892
rs560750736	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169782772	TTTCTATAAGCTATG[C/T]TTATGATTTTTGCAC	55892
rs560957206	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789630	TAGCTGGTACTACAG[A/G]TGCGCGCCACCACAC	55892
rs561348185	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169777908	AAGTGGATTCCTCTA[A/G]GCAACATTGGCATCA	55892
rs561553041	snp	A/G	0.000675971	0.0183719	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169779359	GAGTCCTTATGAGGC[A/G]GAGAACTCCGGGGAA	55892
rs561763725	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783629	TGTAAACCTTGACTT[C/T]TAAGCCATTATGGAC	55892
rs562084265	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169775907	ATTAATCCTTTTGAC[A/G]AGGAAACATTCTTGT	55892
rs562304501	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773572	GGCGCAGGTGGAAGG[A/C]TTGGGCTAGGCAGCC	55892
rs562367281	snp	A/G	1.64779e-05	0.00287031	synonymous-codon	ACTRT3	GRCh38.p7	3:169767900	GTAGTTCATTGCCAC[A/G]TAACAAAAGCTCTCC	55892
rs562426929	snp	A/G	6.8861e-05	0.00586735	intron-variant	MYNN	GRCh38.p7	3:169782691	AAGTTATAAATAAAA[A/G]AAAAAGGGGACTTGG	55892
rs562436147	in-del	-/AT	0.0471551	0.14613	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770269	ATATAATTTATATAA[-/AT]ATATGTTATATTATA	55892
rs562499628	snp	A/C			synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169779456	GCCAGCAGTTTGAGA[A/C]GGCACATGAGAATAC	55892
rs562567012	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169781545	AAGAAATCAAAAGAC[A/G]GCCCTGAGGCACTCT	55892
rs562978288	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787886	ATTTATTTCACTGCC[C/T]GATCTTTGGATATGA	55892
rs562987545	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772802	GTGCCCAGCTGCTCC[G/T]CTTTCGTGCATCCCA	55892
rs563025989	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	MYNN	GRCh38.p7	3:169789826	CTACCTTTGGGAAGC[A/C]GTTTAAAATGATGCT	55892
rs563235599	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788414	GTTACCTAATCTCTT[C/G]TGGGTTAAATGTGAT	55892
rs563354568	in-del	-/AT	0.0154538	0.0865337	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770209	TATATATTTATATAA[-/AT]ATATATAAATTTAAA	55892
rs563594296	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169778926	AATTGAATCAACAGA[C/T]TTGTCTTCTTACTCT	55892
rs563766313	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785749	AAGCAGTTTTGTCTG[C/T]GTGACAAGGACGGTG	55892
rs563810470	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	MYNN	GRCh38.p7	3:169771948	TGTGTAATAAAACGC[A/C]TTTCCAGGGAGACAA	55892
rs564081623	in-del	-/CTT			upstream-variant-2KB, cds-indel	MYNN	GRCh38.p7	3:169772316	CACACTAAAAAATCC[-/CTT]TTTTTTTTTTTTTTT	55892
rs564152135	snp	C/G/T	6.88129e-05	0.00586536	synonymous-codon, missense	ACTRT3	GRCh38.p7	3:169769467	CCCAGCCACGCCCGC[C/G/T]TTGATCATTCCCGAG	55892
rs564216300	snp	G/T	0.000798403	0.0199641	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769832	CTAACCCTTCACAAG[G/T]GCATTTCTCAAATAC	55892
rs564304020	in-del	-/T	0.0389318	0.133978	intron-variant	MYNN	GRCh38.p7	3:169783718	TATTTGCTTATTTTG[-/T]TTTTTTTTTAGTTGT	55892
rs564419425	in-del	-/A	0.0372196	0.131242	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770237	TAAATATAAAATATT[-/A]AAAAATATATAAATT	55892
rs564741433	snp	A/C	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768501	GTAAGTGTCAGCCAA[A/C]AATAGCACAGCTACT	55892
rs564748101	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169773005	CGGTGGGGCCCCGAG[A/G]AAGGGGAGGATGATG	55892
rs564748540	in-del	-/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789238	AAATTTTAGAAAACC[-/T]TTTTTTCAAAGGTAA	55892
rs564969886	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169789699	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	55892
rs565016343	in-del	-/TA	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169776030	TTCAAGTGAGTTCTT[-/TA]TAAGTTGATTAAAGG	55892
rs565170707	snp	A/C	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773325	GGCCCCAGAACCTCC[A/C]GCACTGCCACGGGAA	55892
rs565215506	snp	A/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772984	TACACATGCAGCAGT[A/T]TCCACCGGTGGGGCC	55892
rs565420507	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772293	CCCGGTTCGAAACCG[C/G]GCGGAAACACACTAA	55892
rs565575351	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785948	CACAGAATAATATGA[A/G]CAACTTATTAAAAAC	55892
rs565690827	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775448	CTGTTCATAATCTTC[C/T]GACACAGGAAGATTA	55892
rs565753569	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769621	CAGAGGCCCCGGCAC[A/G]GCCGGGTGAGGCCAG	55892
rs565889911	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169775521	CTTGAGCATGATGCA[A/G]TCTCTCTGGGCCTCA	55892
rs565904136	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772136	TTTCTTTAAATACAT[C/T]ATATTCATTCCTCTC	55892
rs565947779	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169785420	GGCATAGTTCTGGTA[C/T]TCAAAGCACTTACAA	55892
rs566010146	snp	A/G	0.0263992	0.111815	intron-variant	ACTRT3	GRCh38.p7	3:169768443	CCGCGTTTATTACCA[A/G]TATCCCTTTATGGGC	55892
rs566030802	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783725	TTATTTTGTTTTTTT[C/T]TTAGTTGTTTGGAGT	55892
rs566205694	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169785174	ATAAAAATGGAAAGC[C/T]AAACAACAAGTTTTG	55892
rs566421754	snp	G/T	8.25621e-05	0.0064245	synonymous-codon	ACTRT3	GRCh38.p7	3:169768208	CCGTGATCTGTTGCC[G/T]GTTGGCCAGTGGGTT	55892
rs566694280	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169783144	CTACATACTTTTATT[C/T]TCCTTTATTAATATA	55892
rs566886446	snp	A/C	0.00119737	0.0244387	downstream-variant-500B	MYNN	GRCh38.p7	3:169790052	CCTTCCCCTCTCCCC[A/C]CAACTACCTAGAACT	55892
rs566903332	snp	A/C	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781594	AGATGGGTGAGAACC[A/C]GCAGAGGTAACTAGG	55892
rs567024151	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773066	CGCAGTGCGCAGCTG[A/G]CTTCAGGAGAGAGGC	55892
rs567088620	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773783	GACAGCAAGCCATGG[C/T]CGGGCGCATTCCCGG	55892
rs567143440	snp	C/T	4.95896e-05	0.00497919	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169780654	ATGTCAGCTAGTCTT[C/T]CATAGTCGCATGCAT	55892
rs567197946	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772312	GAAACACACTAAAAA[A/G]TCCCTTTTTTTTTTT	55892
rs567344228	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787974	TCTTTTTCTTTTTTT[C/T]TCCCCCCACAAGGCT	55892
rs567788036	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787163	TTCATATTTTCGCTC[A/G]TAAAAATTTAGGCGC	55892
rs567907048	snp	G/T			intron-variant	MYNN	GRCh38.p7	3:169776399	GTTCTAACATTCTGT[G/T]CTCTTGGACAGGTTA	55892
rs568043012	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169773064	CACGCAGTGCGCAGC[C/T]GGCTTCAGGAGAGAG	55892
rs568252363	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788013	GTGTGAGATGACATC[A/G]TTTCTTATTTCTGCC	55892
rs568260356	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	ACTRT3	GRCh38.p7	3:169770148	TGTACGCAATTAAAA[C/T]AAAATAGTAGTTCCT	55892
rs568275724	snp	C/G	0.00318978	0.0398085	intron-variant	MYNN	GRCh38.p7	3:169777144	GACAATTTTTAGAAA[C/G]CTGTTGTGATGCTAA	55892
rs568315645	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773961	TTGTAACATAAGTAT[A/G]TCTACTGAGCTTGAA	55892
rs568356034	snp	C/G	0.00557542	0.0525036	intron-variant	MYNN	GRCh38.p7	3:169785075	ATGAAAAAAAAGGGG[C/G]GGGGGGTGGTGTTAT	55892
rs568931468	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169773047	GCAACTACAAGCCCC[C/G]GCACGCAGTGCGCAG	55892
rs569056109	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772434	GCTTAATGTATGCCG[A/G]TCCTTCAAAAGACAT	55892
rs569280948	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787130	GATCAATACATAAAC[C/T]ATGCATAAAAATAAA	55892
rs569506072	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169780474	TTATATTTGTTTTCA[A/G]TTCCAACAGTTAACA	55892
rs569568840	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169786234	GGTGCTTGAACTTAA[C/T]CTTGAGGCCCAGATT	55892
rs569678744	in-del	-/ATAA	0.0154538	0.0865337	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770285	TATATGTTATATTAT[-/ATAA]ATATATTTATATATT	55892
rs569792232	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772255	TGTAGTGGTTATCAC[A/G]TTCGCCTAACACGCG	55892
rs569849935	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772169	TTTGATAATAATCAC[G/T]TGAGAATTGCGAATT	55892
rs570023697	snp	A/G	1.74726e-05	0.00295567	intron-variant	MYNN	GRCh38.p7	3:169780762	AAGGTAAAAAACCAA[A/G]TGAGTTGTTTGATCT	55892
rs570098698	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169782445	AATTGTTTTACTTAT[C/T]TAACTTTATTTACTA	55892
rs570099788	snp	C/T			synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774538	GTTGGAGTTTATATA[C/T]ACAGGAACTTTAAAT	55892
rs570134410	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769663	CGCAGGCAGGGGGTC[G/T]GCAGGGCCCCAGGCG	55892
rs570436942	in-del	-/A	0.00835141	0.0640778	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770367	TATATTTATATTTAT[-/A]TATATGTATAAATAT	55892
rs570474446	snp	A/G			intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169773537	GAGGGCAGGCTCCTT[A/G]GAGTTCCAGCACGGG	55892
rs570530982	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169776981	ATAAGCAACTGCACC[C/T]GGCCTTGAACAATTA	55892
rs570630268	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169783904	CTAAACAGTGTTTAG[C/T]ATGCAATTTTTAGGA	55892
rs570867679	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772320	CTAAAAAATCCCTTT[C/T]TTTTTTTTTTTTTTT	55892
rs571076631	snp	A/G	0.000399281	0.0141238	intron-variant	ACTRT3	GRCh38.p7	3:169768919	CCACATTATAGTATA[A/G]TTTAAATGTCAATTG	55892
rs571577200	snp	C/G	3.30447e-05	0.00406464	missense	ACTRT3	GRCh38.p7	3:169768242	CGCTGGCTCAGTAAT[C/G]AAGACTGGGCCATCA	55892
rs571627140	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, intron-variant	MYNN	GRCh38.p7	3:169774072	CACTTATTGATGTGT[A/C]CAAAGGATTGTGTTA	55892
rs571722563	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788043	CATGCTGTGGCTTTT[C/T]TGTGTTCTGCTTTTA	55892
rs571767110	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	MYNN	GRCh38.p7	3:169789753	CAAAGTGCTGGGATT[A/G]TAGGCATGAGCCACT	55892
rs571794769	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169783185	AGAATAGAAATGTGG[A/G]TTTATGAATTGACAT	55892
rs572056891	snp	G/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169784340	ACTAAATGTTTCATA[G/T]AAATACAAGAGTAGG	55892
rs572102763	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769817	TCAAAAGATTCAACT[C/G]TAACCCTTCACAAGT	55892
rs572631684	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169778246	AATCTCAGGCCCCAT[C/T]ACAGACCTACTGAAT	55892
rs572672978	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773277	GTCTCTGTGGTACAT[C/T]CTGTACCGCCCTGGC	55892
rs572735755	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774172	ATTTTCAAGGGGGCT[A/G]AAATTGTTTAAGTTA	55892
rs572737176	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789635	GGTACTACAGGTGCG[C/T]GCCACCACACCTGAC	55892
rs573237667	in-del	-/ATAA	0.0402882	0.136092	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770599	TTATATTTATATATC[-/ATAA]ATATATAAAAATTTA	55892
rs573297499	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788341	TTATCTAAGAAATCT[A/G]TGCATGTGTATCAAG	55892
rs573302126	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169780056	ACGTTTACATTCGTA[C/T]TTTTTTCTTTTTTTT	55892
rs573303929	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772285	GAAAGGTCCCCGGTT[C/T]GAAACCGGGCGGAAA	55892
rs573384896	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169778716	TATGCAGCTCTGTTT[C/T]GAAAGTTTTTCTTTG	55892
rs573392744	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771750	TGCATACATCTGTAG[A/G]GAATTTGAAAACAAG	55892
rs573568791	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772588	AGCTAACACTGAAAA[A/C]ATAATGTACAGCCTA	55892
rs573625472	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169783191	GAAATGTGGGTTTAT[A/G]AATTGACATGTTCTT	55892
rs573801541	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787478	GGAAAATGTACTTGA[A/G]TTTTGAAATATTTTG	55892
rs573862982	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169776853	GAATTACAGGCACCC[A/G]CCATCATGCCCAGCT	55892
rs573925210	snp	C/T	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169777452	TTTAGGGAAAAAAAT[C/T]AAGTAGGAAGATTAT	55892
rs574227520	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169777002	TGAACAATTAATGTA[C/T]GACTTCCTGCTAACT	55892
rs574252264	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785488	AATAAACTAAATAAA[C/T]AGGGAAAATGTAGGG	55892
rs574255239	in-del	-/GTAAAT	0.00600419	0.0545855	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770567	TTATATTTATATATC[-/GTAAAT]ATAAATATATAAAAA	55892
rs574423419	snp	A/C			utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769624	AGGCCCCGGCACGGC[A/C]GGGTGAGGCCAGAGT	55892
rs574502488	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769724	ATGTTACCGCCCGCT[A/G]TTGCTTCTCGCAGGA	55892
rs574515625	snp	C/T	0.0023933	0.0345097	intron-variant	MYNN	GRCh38.p7	3:169775079	AATTCTAAGTTACTT[C/T]CAGTTTCCCATTGCT	55892
rs574778335	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169775556	CCCCATCTGTCAAAA[C/T]GAGATGGTAATAACT	55892
rs575058416	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169780300	CCTGAACTCGTGATC[C/T]GCCCGCCTCCGCCTT	55892
rs575126911	snp	C/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169781105	AGGCCAGGGTGGCAG[C/T]AGTGAAAGAAATAAG	55892
rs575181191	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789600	CAAGCAATTCTCCGG[C/G]CTCAGCCTCCTGAGT	55892
rs575279303	in-del	-/ATAA	0.00758169	0.0611013	upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770568	TTATATTTATATATC[-/ATAA]ATATATAAAAATTTA	55892
rs575738629	snp	A/G	0.00119737	0.0244387	intron-variant	MYNN	GRCh38.p7	3:169778633	TGAATTTATAAATCT[A/G]TTTTTCTCTTAGTTA	55892
rs575746013	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772278	AACACGCGAAAGGTC[A/C]CCGGTTCGAAACCGG	55892
rs575813548	snp	C/T	5.13932e-05	0.00506892	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786701	AGGAATATGGAATTG[C/T]TAAGATATCATTGGT	55892
rs575836672	snp	A/G/T	0.00239401	0.0345304	upstream-variant-2KB	MYNN	GRCh38.p7	3:169772229	CCCTCTCCAAAGTGG[A/G/T]GTTTCCGTAGTGTAG	55892
rs575926551	snp	C/G			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788614	GTTGCCAAATTTCCT[C/G]TGGTATTATTAGCAT	55892
rs575944237	snp	A/T	1.68952e-05	0.00290642	intron-variant	MYNN	GRCh38.p7	3:169782416	TGAATTCTTGCTATA[A/T]AGACTGACCTCCAAA	55892
rs576001456	snp	A/G	0.00163306	0.0285283	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779141	GTTGAATTATTCCTA[A/G]ATGCAAATAAACTGC	55892
rs576023292	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	MYNN, ACTRT3	GRCh38.p7	3:169771712	ACATTGCATGTCAAT[A/G]AACGCATCTTGGTGT	55892
rs576047094	snp	G/T	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169776774	AATGGCGTGATCTCG[G/T]CTCACTGCAACCTCC	55892
rs576258104	snp	A/G	0.000399281	0.0141238	intron-variant	MYNN	GRCh38.p7	3:169785428	TCTGGTACTCAAAGC[A/G]CTTACAACCTGGTGT	55892
rs576762414	snp	C/G	0.00279162	0.0372561	upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772704	TGGCTGTAAATAATC[C/G]TATTAAAAATCTTCT	55892
rs576891992	snp	C/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788887	TTATCATAATATGCA[C/T]ATATTTAGTTGTATC	55892
rs576934527	snp	A/G	0.000798403	0.0199641	intron-variant	MYNN	GRCh38.p7	3:169774982	TAACTGGGACTACAG[A/G]TGTGCACTACCACAC	55892
rs577077796	snp	A/T	4.97187e-05	0.00498567	utr-variant-5-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169774277	TAGATCAAGGGTAAA[A/T]TTCCATTCTGATATC	55892
rs577205912	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	MYNN	GRCh38.p7	3:169773098	CGCGGTGCTGTGCTG[C/T]CGGGCCTCGGCGCAG	55892
rs577459674	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	MYNN	GRCh38.p7	3:169789257	TTTCAAAGGTAATGG[C/T]TCTATCAGTTTCATT	55892
rs577719880	in-del	-/TGT	0.00199481	0.0315187	cds-indel, nc-transcript-variant	MYNN	GRCh38.p7	3:169787989	TTCCCCCCACAAGGC[-/TGT]TGTTCAGTGTGAGAT	55892
rs577993235	snp	C/T	1.65299e-05	0.00287483	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786595	GTCACGGATACTCAG[C/T]CTCCTACATCAGATA	55892
rs578205765	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787350	TTGAGTTATCTGAGA[C/T]TGTATTTTCAAAATG	55892
rs745331332	snp	C/T	5.40497e-05	0.00519826	intron-variant	MYNN	GRCh38.p7	3:169784758	TTTTAATTTGGTGCT[C/T]ATATTAGTGCTATTC	55892
rs745341453	snp	A/G	1.64947e-05	0.00287177	synonymous-codon	ACTRT3	GRCh38.p7	3:169767660	AGAGGTTGATCCCCC[A/G]GCAAGGATAATATTG	55892
rs745439215	snp	A/C			intron-variant	MYNN	GRCh38.p7	3:169785912	AAATATATGAAAGTG[A/C]CATACATACTGTTCT	55892
rs745605259	snp	A/T			intron-variant	MYNN	GRCh38.p7	3:169780561	AAAACACTATTTTCT[A/T]CTAAATATAAATTTT	55892
rs745623878	snp	A/C/G	6.99466e-05	0.00591349	intron-variant	ACTRT3	GRCh38.p7	3:169768365	ACTGTAAGGAAAGCA[A/C/G]TAAGATCAATGACAG	55892
rs745645728	snp	A/G	3.29821e-05	0.00406078	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779264	ATTGTGCACACTGTT[A/G]CAGTGAAACGGAAAC	55892
rs745683785	in-del	-/A	1.82134e-05	0.00301768	intron-variant	MYNN	GRCh38.p7	3:169779584	GGTGTGTGGGGAGAT[-/A]ATTATTTTTATACTG	55892
rs745777015	in-del	-/A	1.66905e-05	0.00288876	frameshift-variant, intron-variant, nc-transcript-variant	MYNN	GRCh38.p7	3:169784660	TATGTGGAAATTCTT[-/A]ACACAGATATTAAAA	55892
rs745810635	snp	C/T			upstream-variant-2KB	MYNN	GRCh38.p7	3:169772187	AGAATTGCGAATTGA[C/T]ACTTACATATCAAGG	55892
rs745899599	snp	A/G			missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779466	TGAGAAGGCACATGA[A/G]AATACATAAAGGAGT	55892
rs745904851	snp	G/T	4.94931e-05	0.00497434	synonymous-codon, nc-transcript-variant, intron-variant	MYNN	GRCh38.p7	3:169778876	TATTGCTAATCCTTC[G/T]TCTACAGAGATATCT	55892
rs746097772	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169777509	TGTGTGTGTTTCCAT[C/T]CTCAAATACTTATAA	55892
rs746102434	snp	G/T	6.61868e-05	0.00575231	intron-variant	MYNN	GRCh38.p7	3:169783612	CTCTTAATTTCTTTT[G/T]ATGTAAACCTTGACT	55892
rs746125870	snp	C/T	1.80179e-05	0.00300143	intron-variant	MYNN	GRCh38.p7	3:169778739	TTTCTTTGATCAGAA[C/T]ATTGTCATGTAGCCT	55892
rs746166395	snp	A/C			downstream-variant-500B	MYNN	GRCh38.p7	3:169790145	CAATATTGATATGTA[A/C]TTATTACAGCATTAA	55892
rs746213520	snp	C/T	1.82347e-05	0.00301944	intron-variant	MYNN	GRCh38.p7	3:169779586	GTGTGTGGGGAGATA[C/T]TATTTTTATACTGTG	55892
rs746349240	in-del	-/CTT			intron-variant	MYNN	GRCh38.p7	3:169775506	CAGTCGCTATGTCTC[-/CTT]GAGCATGATGCAATC	55892
rs746502406	snp	A/T	1.6516e-05	0.00287362	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786587	TTCTGCCTGTCACGG[A/T]TACTCAGTCTCCTAC	55892
rs746586520	snp	A/T			intron-variant	MYNN	GRCh38.p7	3:169781931	TTTTTAATATGGGAG[A/T]CATCAGTATATTTGT	55892
rs746657214	snp	C/T			intron-variant, upstream-variant-2KB	MYNN	GRCh38.p7	3:169774197	AAGTTATGTCCTCTG[C/T]CCCTTCCCTCACTGA	55892
rs746673317	snp	G/T	3.29582e-05	0.00405931	missense	ACTRT3	GRCh38.p7	3:169767804	ACAAGAAAAGAGCTG[G/T]TCATGGAGCTGGATG	55892
rs746696845	snp	A/G	1.6492e-05	0.00287154	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786475	AGTGAACAGGATTCC[A/G]TACAAAAAAGTCCTT	55892
rs746732761	in-del	-/T	0.000388401	0.0139302	intron-variant	MYNN	GRCh38.p7	3:169786394	TAAAGATAATGTAGA[-/T]TTTTTTTTCCTTCCA	55892
rs746764211	snp	A/G			utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769664	GCAGGCAGGGGGTCG[A/G]CAGGGCCCCAGGCGG	55892
rs746880942	snp	C/T	3.29821e-05	0.00406078	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779273	ACTGTTACAGTGAAA[C/T]GGAAACGTGGAAAAT	55892
rs746931344	snp	C/G			intron-variant	MYNN	GRCh38.p7	3:169784904	TTTTTCATATTGAAT[C/G]TCTTATTTAAAAAAA	55892
rs746961811	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169784431	AGATACAGATTTTTT[A/G]TATAAAGGAGTGTCT	55892
rs747011938	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169776233	TTGGTACATATCTTT[C/T]CTGGAGACTGGGGAG	55892
rs747030413	snp	C/T	1.65201e-05	0.00287398	synonymous-codon	ACTRT3	GRCh38.p7	3:169768227	GGCCAGTGGGTTCAG[C/T]GCTGGCTCAGTAATC	55892
rs747161611	snp	C/T	1.672e-05	0.00289132	missense, intron-variant, nc-transcript-variant	MYNN	GRCh38.p7	3:169784633	TCAGGAGAAAGACCA[C/T]TTATCTGCGAATTAT	55892
rs747173245	snp	A/G	1.65707e-05	0.00287838	synonymous-codon	ACTRT3	GRCh38.p7	3:169768326	GTCCTCCCATGAAGT[A/G]ATGAGACCACGCTCC	55892
rs747216437	snp	A/G			synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779038	AAAGTCATCTCAAAC[A/G]AAAAAGAAGAAGAAG	55892
rs747312323	snp	G/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169782512	ATAGGTGTGGACAGA[G/T]ATTTGCTCAAGCCAG	55892
rs747446074	snp	A/G	1.64898e-05	0.00287135	missense	ACTRT3	GRCh38.p7	3:169767680	GGATAATATTGGAAA[A/G]GAAGGAATTCCTCAG	55892
rs747581519	snp	A/G	1.65449e-05	0.00287614	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169780689	GTGAAGAAAAACCCT[A/G]TAAATGTGATGTATG	55892
rs747631092	snp	A/G	8.24545e-05	0.00642032	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169779369	GAGGCGGAGAACTCC[A/G]GGGAAGAGCTGGATC	55892
rs747644757	snp	G/T			intron-variant	MYNN	GRCh38.p7	3:169776780	GTGATCTCGGCTCAC[G/T]GCAACCTCCACCTCC	55892
rs747680723	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169779943	TTGACTTCTGAACAT[A/G]TTCATTGGAATTACA	55892
rs747696403	snp	C/T	1.65551e-05	0.00287702	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169786614	CTACATCAGATACAT[C/T]GTTGAGGTCAACTGT	55892
rs747726322	snp	A/C	1.85194e-05	0.00304292	missense	ACTRT3	GRCh38.p7	3:169769382	AGAGTTCTAGCCCGC[A/C]CTGGGCCGCGCGGCT	55892
rs747828571	snp	A/C/T	6.59658e-05	0.00574277	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779279	ACAGTGAAACGGAAA[A/C/T]GTGGAAAATCACAGC	55892
rs747848509	snp	A/G			downstream-variant-500B	MYNN	GRCh38.p7	3:169789779	CCACTGCGCCCAACC[A/G]TGAACTACTATCTTA	55892
rs747927902	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169781595	GATGGGTGAGAACCA[A/G]CAGAGGTAACTAGGA	55892
rs747942622	snp	G/T	2.6419e-05	0.00363439	intron-variant	MYNN	GRCh38.p7	3:169783688	TAGCAATATCTTAAT[G/T]TATAAATATCAACTT	55892
rs748041393	snp	C/G			missense	ACTRT3	GRCh38.p7	3:169768055	GCAGACAGTAACCCT[C/G]AAAGATGGGCACACT	55892
rs748160662	snp	C/T	1.65894e-05	0.00288	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169780708	ATGTGATGTATGCAA[C/T]TTACAGTTTGCAACT	55892
rs748295145	snp	A/G	6.59805e-05	0.00574333	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774499	TGATCAGAGTCAGGT[A/G]AAGGCTGATGGATTT	55892
rs748365710	in-del	-/TTAT	1.6773e-05	0.0028959	intron-variant	MYNN	GRCh38.p7	3:169782440	TCCAAATTGTTTTAC[-/TTAT]TTATTTAACTTTATT	55892
rs748392096	snp	A/G	1.66829e-05	0.00288811	synonymous-codon	ACTRT3	GRCh38.p7	3:169768347	ACCACGCTCCACTGG[A/G]TAACTGTAAGGAAAG	55892
rs748405832	snp	C/G			missense	ACTRT3	GRCh38.p7	3:169767790	AAGAGGGCCTCTGGA[C/G]AAGAAAAGAGCTGGT	55892
rs748473002	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169777180	ATAAGGGGAAACATA[C/T]AGGTGGCACTTGAGG	55892
rs748517260	snp	A/G	1.64789e-05	0.0028704	synonymous-codon	ACTRT3	GRCh38.p7	3:169767828	CTGGATGACCTTCCC[A/G]TCAGGTAGTTGGTAA	55892
rs748522603	snp	G/T	1.64817e-05	0.00287064	synonymous-codon	ACTRT3	GRCh38.p7	3:169767978	ACCATGGTTCTTCAT[G/T]AGCACCATGAGGTAG	55892
rs748585458	snp	A/G	9.88452e-05	0.00702942	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169782574	GGAGAAAAGCCTTAT[A/G]TATGTGATACCTGTG	55892
rs748667393	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169775513	TATGTCTCCTTGAGC[A/G]TGATGCAATCTCTCT	55892
rs748715535	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169774463	GATCTACAGAAGCAC[C/T]TCTGAGAACAATGTC	55892
rs748758290	snp	C/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169788053	CTTTTTTGTGTTCTG[C/T]TTTTAAACTACACCT	55892
rs748768940	in-del	-/G	1.64928e-05	0.00287161	frameshift-variant, nc-transcript-variant	MYNN	GRCh38.p7	3:169779369	GAGGCGGAGAACTCC[-/G]GGGAAGAGCTGGATC	55892
rs748797368	snp	A/G	1.6609e-05	0.0028817	missense	ACTRT3	GRCh38.p7	3:169769474	ACGCCCGCCTTGATC[A/G]TTCCCGAGCCGTTGT	55892
rs748804665	snp	A/T	1.77373e-05	0.00297797	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769561	GTCTCTGAGCCGCTC[A/T]AGCTACGGGCTCGGC	55892
rs748821120	snp	C/G	0.000115431	0.00759618	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169779401	GAGGTATTCCAAGGC[C/G]AAGCCAATGTGTAAC	55892
rs748956457	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169786162	ATGTGTGATTAAGCC[A/G]ATATAACAGCTCACC	55892
rs748995902	snp	A/G	8.73904e-05	0.00660966	intron-variant	MYNN	GRCh38.p7	3:169779569	TCATACAGGTGAGAC[A/G]GGTGTGTGGGGAGAT	55892
rs749019744	snp	A/T			upstream-variant-2KB	ACTRT3, MYNN	GRCh38.p7	3:169770969	ATAAATATATAAAAA[A/T]TTATATTTATATATC	55892
rs749066571	snp	A/G	1.65603e-05	0.00287747	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779051	ACGAAAAAGAAGAAG[A/G]AGGCTTTCAACTCCC	55892
rs749172767	in-del	-/G	1.65296e-05	0.00287481	frameshift-variant	ACTRT3	GRCh38.p7	3:169768274	ACGGCTTCAGCTTTA[-/G]GTTATAGTCATAGAT	55892
rs749289157	in-del	-/T			intron-variant	MYNN	GRCh38.p7	3:169784863	TGTGAGGAAAGTAGC[-/T]TTTTTGCAGAAACAT	55892
rs749312407	snp	A/G			synonymous-codon	ACTRT3	GRCh38.p7	3:169767858	AACTTTCTCTAGACA[A/G]TCGGGTTTCTTGGCC	55892
rs749355707	in-del	-/A	1.71876e-05	0.00293147	utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169786707	TGGAATTGCTAAGAT[-/A]ATCATTGGTAGCAAA	55892
rs749440250	snp	A/G	5.19188e-05	0.00509477	intron-variant	MYNN	GRCh38.p7	3:169774602	TATAAAAGCTAGTCA[A/G]TAGTCTTCACAGCAA	55892
rs749486407	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169780955	GGAAATAAGGTCAGA[C/T]TCGTCCAGAAGTAAG	55892
rs749546554	snp	G/T	3.29533e-05	0.00405901	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169782595	GATACCTGTGGGAAG[G/T]CATTTGCTGTCTCTA	55892
rs749574271	snp	C/G	1.651e-05	0.0028731	synonymous-codon	ACTRT3	GRCh38.p7	3:169768134	AGCAGCAAAGAGAGC[C/G]AGCACAGCCTGGATG	55892
rs749813600	snp	C/G	1.64893e-05	0.0028713	missense	ACTRT3	GRCh38.p7	3:169768019	CAAGGCCTGCCAGAT[C/G]CAGTTGCTGCACACC	55892
rs750063856	snp	A/G			intron-variant	MYNN	GRCh38.p7	3:169776870	CATCATGCCCAGCTA[A/G]TTTTTGTATTTTGTA	55892
rs750064507	snp	A/G			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787237	ATAACTTTTCTAATG[A/G]AACAAAAATGTTTCT	55892
rs750115126	snp	C/T	1.67382e-05	0.00289289	intron-variant	MYNN	GRCh38.p7	3:169782444	AAATTGTTTTACTTA[C/T]TTAACTTTATTTACT	55892
rs750138708	snp	C/T	0.000132098	0.00812599	missense	ACTRT3	GRCh38.p7	3:169768081	ACACTCTGGGTAACC[C/T]CAGCACCTGAATTCA	55892
rs750236928	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772809	GCTGCTCCGCTTTCG[G/T]GCATCCCAGACTTCT	55892
rs750243131	snp	C/T	1.64901e-05	0.00287137	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169779338	GTCTAATATAGCCAG[C/T]GTCAAGAGTCCTTAT	55892
rs750391874	snp	A/G			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787867	CCACTTTTCCCACAT[A/G]TTAATTTATTTCACT	55892
rs750397700	snp	C/G	3.30262e-05	0.0040635	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169786582	CATGCTTCTGCCTGT[C/G]ACGGATACTCAGTCT	55892
rs750575228	snp	A/G	1.65304e-05	0.00287488	missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169780659	AGCTAGTCTTCCATA[A/G]TCGCATGCATCATGG	55892
rs750582978	snp	A/G	1.65759e-05	0.00287883	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779020	ACAAGGCGCGTTAGC[A/G]AAAAAGTCATCTCAA	55892
rs750665981	snp	C/T	1.74592e-05	0.00295454	utr-variant-5-prime	ACTRT3	GRCh38.p7	3:169769534	ATGCCGCCGCTGCTG[C/T]CGCCGCCTCCTGTCT	55892
rs750747641	snp	C/T	1.6537e-05	0.00287545	stop-gained	ACTRT3	GRCh38.p7	3:169768296	GTCATAGATATGCTT[C/T]CACATGATCTCCATG	55892
rs750758184	snp	A/C	1.65021e-05	0.00287241	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779196	CACAAATAAATGATA[A/C]TTCAGAACTCGAGTT	55892
rs750800437	snp	C/T			missense, nc-transcript-variant	MYNN	GRCh38.p7	3:169782547	CTGACCTATCATGTC[C/T]GTAGGCATACTGGAG	55892
rs750837402	snp	A/C	0.000359002	0.013393	intron-variant	ACTRT3	GRCh38.p7	3:169769271	CCCTACCCCACCCCC[A/C]CCCCACCCACCCTCC	55892
rs750895259	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772314	AACACACTAAAAAAT[C/T]CCTTTTTTTTTTTTT	55892
rs750905911	snp	A/G	1.65252e-05	0.00287443	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779084	AAAACAGGGCAGAAT[A/G]AAACAGTGCAATATC	55892
rs750994790	in-del	-/AT			intron-variant	MYNN	GRCh38.p7	3:169774573	ACAGGTAAAGTACAC[-/AT]TTTATTTTCAGTTAT	55892
rs751070468	snp	A/G	1.691e-05	0.0029077	synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169778813	TGACTATCTCAAAGT[A/G]GAAGAGGTGGTCACT	55892
rs751076684	snp	C/T	1.64789e-05	0.0028704	missense	ACTRT3	GRCh38.p7	3:169767962	CACTGAGCAACATGA[C/T]ACCATGGTTCTTCAT	55892
rs751134596	snp	C/T			intron-variant	MYNN	GRCh38.p7	3:169776654	GATTATAGCCATCTA[C/T]GAAATAGTTTGTATG	55892
rs751168471	snp	A/T	6.60546e-05	0.00574656	missense	ACTRT3	GRCh38.p7	3:169768093	ACCCCAGCACCTGAA[A/T]TCAGCACAAGGCCAG	55892
rs751180330	snp	A/G	1.64841e-05	0.00287085	missense, nc-transcript-variant, intron-variant	MYNN	GRCh38.p7	3:169783537	CCTCAGGAGAGCTCA[A/G]CAAACACTTTCGGTC	55892
rs751268494	snp	A/G	5.05693e-05	0.00502813	intron-variant	MYNN	GRCh38.p7	3:169774567	ATCTTGACAGGTAAA[A/G]TACACATTTTATTTT	55892
rs751322574	snp	G/T	1.66651e-05	0.00288657	synonymous-codon, nc-transcript-variant	MYNN	GRCh38.p7	3:169779542	TAACCAGCTGAAAAC[G/T]CATGTAAGAACTCAT	55892
rs751370499	snp	C/T	1.72279e-05	0.0029349	missense	ACTRT3	GRCh38.p7	3:169769447	ATAAACTGGGGCTCC[C/T]GGCACCCAGCCACGC	55892
rs751402144	snp	A/T			utr-variant-3-prime, nc-transcript-variant	MYNN	GRCh38.p7	3:169787608	GGCTTCTAAATTTGG[A/T]ACATTATATTGCATA	55892
rs751410436	snp	G/T	3.65324e-05	0.00427374	intron-variant	MYNN	GRCh38.p7	3:169780580	AATATAAATTTTATT[G/T]TTCCTTTAGGTGAGA	55892
rs751623996	snp	A/G	3.30278e-05	0.0040636	missense, nc-transcript-variant, utr-variant-5-prime	MYNN	GRCh38.p7	3:169779097	ATAAAACAGTGCAAT[A/G]TCCCAGTGACATCTT	55892
rs751696163	in-del	-/T			upstream-variant-2KB, utr-variant-5-prime	MYNN	GRCh38.p7	3:169772270	TTCGCCTAACACGCG[-/T]AAAGGTCCCCGGTTC	55892

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