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

RFWD3

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1138860	snp	C/G	0.340784	0.232934	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621736	ACTGCACTCCAGCCT[C/G]GGTGACAGAGCAAGA	55159
rs1138861	snp	A/C	0.456332	0.141164	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621703	CCATCTCAAAAAAAA[A/C]AAACAAACAAAAAAA	55159
rs1802616	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668314	AAAGAAACCATTGAC[A/C]AGAGCTGAAGTGGGA	55159
rs3202910	snp	A/C	0.161267	0.233723	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621707	GACTCCATCTCAAAA[A/C]AAACAAACAAACAAA	55159
rs3205212	snp	A/C	0	0	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623503	CCTTGAAGGGACTAA[A/C]CATCGTCTTGGTACT	55159
rs3208607	snp	C/T	0	0	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668689	ATTCTTCCTGATGAC[C/T]CTAGAAAACCCAACT	55159
rs3208608	snp	C/T	0.1128	0.208988	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668698	GATGACTCTAGAAAA[C/T]CCAACTGAATGGTAT	55159
rs3208609	snp	C/T	0.131038	0.219882	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668770	GTGTTGAAGAACATT[C/T]GTGTACGCTTTTTGA	55159
rs3208610	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668777	AGAACATTCGTGTAC[A/G]CTTTTTGACTCCAAG	55159
rs3208611	snp	G/T	0	0	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668781	CATTCGTGTACGCTT[G/T]TTGACTCCAAGAACT	55159
rs3923862	snp	C/G	0.202959	0.245534	intron-variant	RFWD3	GRCh38.p7	16:74658924	AAAAATTAGCCGGGC[C/G]TGGTGGCACACACCT	55159
rs4072450	snp	C/G	0.347914	0.230028	intron-variant	RFWD3	GRCh38.p7	16:74632736	GAGCTACTTGAAAAA[C/G]TAGTTTGAATTGCCC	55159
rs4243108	snp	C/T	0.3512	0.228601	intron-variant	RFWD3	GRCh38.p7	16:74658555	TTCAGAAGTTATAAG[C/T]GATTAGTCCTGGGAA	55159
rs4271617	snp	C/T	0.336017	0.234736	intron-variant	RFWD3	GRCh38.p7	16:74640373	ctggtctcgaacttc[C/T]gaccttgtgatccgc	55159
rs4286131	snp	C/G	0.335788	0.23482	intron-variant	RFWD3	GRCh38.p7	16:74642143	CCTTTTTAAAtttga[C/G]acagagtcttgctct	55159
rs4287593	snp	C/T	0.336017	0.234736	intron-variant	RFWD3	GRCh38.p7	16:74642652	GTGTACCACTACACA[C/T]GGATAATTTTTTTCA	55159
rs4346229	snp	C/G	0.199873	0.244923	intron-variant	RFWD3	GRCh38.p7	16:74640109	TCCTTGTGGCTAAGG[C/G]GGGACTACTGTAGCC	55159
rs4395097	snp	C/T	0.206029	0.246103	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668532	TGTTCCCTTGGCAGA[C/T]GTCAAGTGAGAAAAT	55159
rs4402594	snp	C/T	0.462909	0.131034	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667462	AATCTCAAACCGCTG[C/T]AAGGGATCTGAGCTA	55159
rs4448975	snp	A/G	0.207253	0.246318	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668356	CAGGAAAGAAGAGTA[A/G]AAAGGGATATTCTTA	55159
rs4462623	snp	C/T	0.3512	0.228601	intron-variant	RFWD3	GRCh38.p7	16:74658528	CCACACTGAGAAATT[C/T]ATCTCAAGAAATTCA	55159
rs4500770	snp	A/T	0.414245	0.188477	intron-variant	RFWD3	GRCh38.p7	16:74624532	tcccaagtagctggg[A/T]ttacagacatccacc	55159
rs4531752	snp	C/T	0.202035	0.245356	intron-variant	RFWD3	GRCh38.p7	16:74634962	GCCTGACCAAAATGT[C/T]AAAACCCCATTTCAA	55159
rs4544266	snp	A/C	0.362941	0.223034	intron-variant	RFWD3	GRCh38.p7	16:74627095	AGTCTTGGAGACAGC[A/C]GAGCTGTGGGATGAT	55159
rs4558441	snp	A/G	0.0252325	0.109451	intron-variant	RFWD3	GRCh38.p7	16:74628149	TCTCAAGGTGGCTCA[A/G]TGACCTAGAGCTGGC	55159
rs4564599	snp	C/T	0.335101	0.23507	intron-variant	RFWD3	GRCh38.p7	16:74635343	ATGGTGGCATGCACC[C/T]GTAGTCTCAACTACT	55159
rs4887780	snp	A/G	0.499946	0.00519141	downstream-variant-500B	RFWD3	GRCh38.p7	16:74620991	taaaaaaaaaaaaaa[A/G]aaaaaaggccgggtg	55159
rs4887781	snp	C/G	0.394904	0.203722	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621252	ACTGCACTCCAGCTA[C/G]GGCTACAGAGCAAGA	55159
rs4887782	snp	C/T	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74627682	gggtacctgccagta[C/T]aaacaagtttcctgt	55159
rs4887783	snp	C/G	0.451109	0.148509	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666845	CTCGGTAGTTACCTC[C/G]GCCGCACTCCGAATG	55159
rs4888262	snp	C/T	0.494848	0.0504932	synonymous-codon	RFWD3	GRCh38.p7	16:74636560	CTGACTTTGATGTGA[C/T]GTAAGTTTTTGCAAG	55159
rs4888263	snp	A/G	0.201418	0.245234	intron-variant	RFWD3	GRCh38.p7	16:74636923	TTACCACGTTGGCCG[A/G]GCTGGTCTTGAACTC	55159
rs4888264	snp	G/T	0.447938	0.152711	intron-variant	RFWD3	GRCh38.p7	16:74647734	GTAGCTGGGATTATA[G/T]GCGCCTGCCAACATA	55159
rs4888265	snp	C/T	0.446902	0.154045	intron-variant	RFWD3	GRCh38.p7	16:74649839	CCCCTCTGTTTGTCA[C/T]TGATTTGTCAGGTCA	55159
rs4888266	snp	C/T	0.352504	0.228019	intron-variant	RFWD3	GRCh38.p7	16:74653906	AAGATTTTTTGACCT[C/T]TTAAAAAAAGAAATG	55159
rs4888267	snp	A/G	0.449599	0.150533	intron-variant	RFWD3	GRCh38.p7	16:74654008	AAAATCCACAATTTA[A/G]AAGTGTTCAATTCAG	55159
rs4888268	snp	A/G	0.194902	0.243853	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664489	GGAGCTGTGGCCCAC[A/G]CCTATAATCCCAGCA	55159
rs4888269	snp	G/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664530	CTGAGGCAGGTAGCT[G/T]GAGACCAGGAGTTGG	55159
rs4888270	snp	A/G	0.351635	0.228408	intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664678	CCCTTGAACCCGGAG[A/G]GTGGAGGTTACATTG	55159
rs4888271	snp	A/T	0.471863	0.115225	intron-variant	RFWD3	GRCh38.p7	16:74666220	GATAGATAGATAGAT[A/T]GATTGATTAGATACA	55159
rs4888272	snp	A/C	0.333491	0.235646	intron-variant	RFWD3	GRCh38.p7	16:74666342	TAATACAAGTCTTTA[A/C]TCCACAGTTTCCGTG	55159
rs4888273	snp	A/G	0.208779	0.246578	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668764	GTAACTGTGTTGAAG[A/G]ACATTCGTGTACGCT	55159
rs5817920	in-del	-/A	0.375	0.216506	intron-variant	RFWD3	GRCh38.p7	16:74635472	ACTCCATCTCAAAAG[-/A]AAAAAAAAAAATCAA	55159
rs6564152	snp	A/T	0.336017	0.234736	intron-variant	RFWD3	GRCh38.p7	16:74624821	ggcaatacagcaaga[A/T]tccaatctctacaag	55159
rs6564153	snp	A/C	0.336017	0.234736	intron-variant	RFWD3	GRCh38.p7	16:74624825	atacagcaagaatcc[A/C]atctctacaagaaaa	55159
rs6564154	snp	C/T	0.334871	0.235153	intron-variant	RFWD3	GRCh38.p7	16:74651691	GAATACAAAATGCCA[C/T]TACAAAGTGACTAAC	55159
rs6564155	snp	C/G	0.32955	0.237006	intron-variant	RFWD3	GRCh38.p7	16:74660686	AAGACACAATCTGAA[C/G]AACAGCCAATCTCTA	55159
rs7184754	snp	C/T	0.352721	0.227922	intron-variant	RFWD3	GRCh38.p7	16:74633966	atccagcctggaaga[C/T]agaactagatcttct	55159
rs7185722	snp	A/G	0.341685	0.232581	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621950	AAATCACTCACGATC[A/G]TATGAATTTGCTTCC	55159
rs7187928	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74630269	catggctaacatttt[A/T]ttgtattttcagtag	55159
rs7188581	snp	A/T	0.453697	0.14494	intron-variant	RFWD3	GRCh38.p7	16:74639003	tggtatttatgtatc[A/T]aaacatagaaaaggt	55159
rs7188880	snp	A/T	0.494569	0.0518282	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630912	GCAACAGCTCCAGAC[A/T]GGACGTCCAGCATTA	55159
rs7190555	snp	A/G			synonymous-codon	RFWD3	GRCh38.p7	16:74636508	AGGGTGAGCAGCTCA[A/G]GACCCATGCTTGGGA	55159
rs7190631	snp	A/G	0.332568	0.235971	intron-variant	RFWD3	GRCh38.p7	16:74648711	cgggaggcagaggtt[A/G]ttgtggtgagctgag	55159
rs7191665	snp	G/T	0.448066	0.152544	intron-variant	RFWD3	GRCh38.p7	16:74655050	ccaagttatccagaa[G/T]atctagctaagacaa	55159
rs7191863	snp	C/G	0.0618563	0.164627	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664845	GGTGACTCCCATACT[C/G]GACAGCAGAAATACA	55159
rs7191921	snp	A/C/T			missense	RFWD3	GRCh38.p7	16:74636483	TTGTGCTTGTGCTGG[A/C/T]CCTGGCTGGAGGGTG	55159
rs7193541	snp	C/T	0.471681	0.115575	missense, intron-variant	RFWD3	GRCh38.p7	16:74630845	CGTCATATACCAGAA[C/T]TGAACCATTGGCCAG	55159
rs7193959	snp	A/T	0.351418	0.228505	intron-variant	RFWD3	GRCh38.p7	16:74631071	AGAACACACTCATAC[A/T]CCCAAACTATCTGGA	55159
rs7195499	snp	C/G	0.348574	0.229746	intron-variant	RFWD3	GRCh38.p7	16:74660075	TAACAATAATAAAAA[C/G]AAGAAGAAAGAGAAA	55159
rs7196362	snp	A/G	0.103438	0.202533	intron-variant	RFWD3	GRCh38.p7	16:74640955	aaataaataaaaTTC[A/G]CAAAGGTATGAAAAA	55159
rs7199068	snp	C/G	0.466618	0.124806	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664365	CATTAAGCAACTCAG[C/G]CTTCAGGAAGACAAA	55159
rs7201075	snp	C/T	0.219648	0.248151	intron-variant	RFWD3	GRCh38.p7	16:74640822	cgggtgcctgtagtc[C/T]cagctactcgtaagg	55159
rs7201320	snp	G/T	0.448195	0.152377	intron-variant	RFWD3	GRCh38.p7	16:74660160	ATCCAGGCTCCAATA[G/T]CAGTGCTAACTCCTC	55159
rs7203192	snp	C/T	0.0217236	0.101931	intron-variant	RFWD3	GRCh38.p7	16:74650356	gtagattcagggctt[C/T]tttttttttttggca	55159
rs7203847	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74630272	ggctaacattttttt[G/T]tattttcagtagaga	55159
rs7204804	snp	C/T	0.338069	0.233974	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623523	TCCCTTCAAGGATAC[C/T]TAAGTGACAGGACAA	55159
rs7205838	snp	A/C	0.450357	0.149522	intron-variant	RFWD3	GRCh38.p7	16:74639002	atggtatttatgtat[A/C]taaacatagaaaagg	55159
rs7342706	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666994	GGGTCCCCCGATAGC[G/T]GAAGCAGCGGTGCTC	55159
rs7342732	snp	A/C	0.351635	0.228408	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664818	TCAACTGCTAGAAAC[A/C]CACATAGGGCGGGTG	55159
rs7499887	snp	A/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662481	ATGTCAATAAACAAA[A/T]ACATGAAAAAAATTA	55159
rs8044278	snp	G/T	0.217851	0.247924	intron-variant	RFWD3	GRCh38.p7	16:74634667	gtgctgggattacag[G/T]catgagccactgtgc	55159
rs8047350	snp	A/C	0.403334	0.197456	intron-variant	RFWD3	GRCh38.p7	16:74645346	tctctgctagagata[A/C]ctcatggatataTag	55159
rs8049056	snp	C/G	0.354665	0.227036	intron-variant	RFWD3	GRCh38.p7	16:74640336	ttcttagtagagaca[C/G]ggtttcatcatgttg	55159
rs8050262	snp	C/T	0.478685	0.10101	intron-variant	RFWD3	GRCh38.p7	16:74627261	tgttacaaatgtgtt[C/T]aatacagttgttacc	55159
rs8050624	snp	A/G	0.353371	0.227628	intron-variant	RFWD3	GRCh38.p7	16:74652792	CTCCTGGAATAACAA[A/G]GCATACTCCAGTTTG	55159
rs8052269	snp	A/G	0.140919	0.224948	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622624	GGTCAGAAGTGTTTT[A/G]TAATAAAAACGATAA	55159
rs8052367	snp	A/G	0.453209	0.145623	intron-variant	RFWD3	GRCh38.p7	16:74624969	actccagcctggacc[A/G]agtaagatactgtca	55159
rs8052923	snp	C/T	0.35207	0.228214	intron-variant	RFWD3	GRCh38.p7	16:74646207	tagcaagaccttgtc[C/T]ctgttaaaaatttaa	55159
rs8055784	snp	C/T	0.333722	0.235565	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663523	gaggccagactggtg[C/T]aggctgaataaatgg	55159
rs8056556	snp	C/G	0.0178098	0.0926698	intron-variant	RFWD3	GRCh38.p7	16:74656716	gcctgcttcagcccc[C/G]caaagtgctgggatt	55159
rs8057095	snp	G/T	0.0854556	0.188216	intron-variant	RFWD3	GRCh38.p7	16:74645726	TTATGCAGCCCATGA[G/T]CATAGTCACAAATAt	55159
rs8058133	snp	A/T	0.450734	0.149016	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623587	TTGATGCCCACTCAC[A/T]TCCTAGATGATGAGA	55159
rs8058261	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74646559	ttgggaggccaaggc[A/G]ggcggatcatgaagt	55159
rs8058880	snp	G/T	0.0659589	0.169201	intron-variant	RFWD3	GRCh38.p7	16:74650420	AGTACTTCCTAAGTG[G/T]CATGAGTATTTCTGA	55159
rs8058922	snp	G/T	0.408511	0.193324	missense	RFWD3	GRCh38.p7	16:74661181	TTGATGTTCTCCACA[G/T]TGTCTTCTCCCAAGA	55159
rs8059780	snp	A/C	0.450609	0.149185	intron-variant	RFWD3	GRCh38.p7	16:74641385	ccaggctggtctcca[A/C]ctcctgacctcagat	55159
rs8060923	snp	A/G	0.209388	0.246679	intron-variant	RFWD3	GRCh38.p7	16:74634823	AAAAAAAAAGGGGGG[A/G]AGGGGGGCGCAGGTA	55159
rs8061670	snp	C/T	0.409382	0.192607	intron-variant	RFWD3	GRCh38.p7	16:74656733	aaagtgctgggatta[C/T]aggcatgagccactg	55159
rs8061942	snp	C/T	0.448708	0.151707	intron-variant	RFWD3	GRCh38.p7	16:74657464	ttcactgacatcacc[C/T]AGGttttctttttct	55159
rs8062783	snp	C/T	0.448708	0.151707	intron-variant	RFWD3	GRCh38.p7	16:74657366	cagtttcctgaatta[C/T]gaaaaagttgatcct	55159
rs9746765	snp	C/T	0.336474	0.234568	intron-variant	RFWD3	GRCh38.p7	16:74656305	agtgagaccttgtct[C/T]gccaaaaaaaaaaaa	55159
rs9922003	snp	C/G	0.0228947	0.104514	intron-variant	RFWD3	GRCh38.p7	16:74639282	gcctcaagtgatcca[C/G]ctgcctcagcctccc	55159
rs9922052	snp	A/C	0.0166325	0.0896639	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666987	CTTCAATGGGTCCCC[A/C]GATAGCTGAAGCAGC	55159
rs9922988	snp	C/T	0.450231	0.149691	intron-variant	RFWD3	GRCh38.p7	16:74635136	atacaaaaaattagc[C/T]gggtgtggtggcggg	55159
rs9923145	snp	A/G	0.450357	0.149522	intron-variant	RFWD3	GRCh38.p7	16:74652268	GAAGCAGGTATAGCA[A/G]ATAAGGGGGGGAGAC	55159
rs9925807	snp	C/G	0.208169	0.246476	intron-variant	RFWD3	GRCh38.p7	16:74645815	tggagtgtagcggca[C/G]aatctcggctcactg	55159
rs9927167	snp	A/C	0.0123036	0.0774623	intron-variant	RFWD3	GRCh38.p7	16:74640774	gaaaccccgtctcta[A/C]taaaaatacaaaaaa	55159
rs9927222	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74632006	TTCAAAGAAACAGGA[A/C]ACATACAGTTTTGTA	55159
rs9929355	snp	A/C	0.00953873	0.0683987	intron-variant	RFWD3	GRCh38.p7	16:74654141	acaagcagtcatttc[A/C]cCTCCTATTTGgtag	55159
rs9929496	snp	A/G	0.450483	0.149354	intron-variant	RFWD3	GRCh38.p7	16:74634575	AATTTTTTTTATAGC[A/G]ATGGAGTCTCACTAT	55159
rs9929568	snp	A/G	0.0228947	0.104514	intron-variant	RFWD3	GRCh38.p7	16:74638343	TGAGATACTCAAATA[A/G]TATAACCCAAAAAAG	55159
rs9929931	snp	C/G	0.450483	0.149354	intron-variant	RFWD3	GRCh38.p7	16:74635004	aactaggcatagccg[C/G]gcgcggtggctcacg	55159
rs9930188	snp	C/T	0.45235	0.146814	intron-variant	RFWD3	GRCh38.p7	16:74634644	TCCTCCCGCCTTGGC[C/T]TCCCAAAGTGCTGGG	55159
rs9931225	snp	C/T	0.444	0.157683	intron-variant	RFWD3	GRCh38.p7	16:74665395	CCAGAATGGCCAATA[C/T]GGTGAAACCCCGTCT	55159
rs9938833	snp	A/G	0.334412	0.235318	intron-variant	RFWD3	GRCh38.p7	16:74638303	TACTGGATTAAAAAG[A/G]AAACAGTAAGCTGTT	55159
rs10637348	in-del	-/GAGA	0	0	intron-variant	RFWD3	GRCh38.p7	16:74626822	AGAAAAACAATTCTG[-/GAGA]TGAGTTGTCTGTTTT	55159
rs10651761	in-del	-/AAA/AAAA	0	0	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664755	TCCGTCTAAAAAAAG[-/AAA/AAAA]AAAAAAGAAAGAAAT	55159
rs10667616	in-del	-/GAGA	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74626821	GAGAAAAACAATTCT[-/GAGA]TGTGAGTTGTCTGTT	55159
rs10673671	in-del	-/TT			intron-variant	RFWD3	GRCh38.p7	16:74657493	TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTCTCGC	55159
rs11149759	snp	C/T	0.428971	0.174555	intron-variant	RFWD3	GRCh38.p7	16:74628699	AAACTGTATCTCACA[C/T]TCCAAAACTCGGACG	55159
rs11276299	in-del	-/CCG/CCGCCGAAGACTCGGTAGTTACCT	0.45762	0.139261	utr-variant-5-prime, splice-donor-variant	RFWD3	GRCh38.p7	16:74666819	GGGCTCGCGAGCCCG[-/CCG/CCGCCGAAGACTCGGTAGTTACCT]CCGAAGACTCGGTAG	55159
rs11327273	in-del	-/A	0.362732	0.22314	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622463	AACATCTATTTCTAC[-/A]AAAAAATTTAAAAAA	55159
rs11414908	in-del	-/C/T	0	0	intron-variant	RFWD3	GRCh38.p7	16:74651003	TATTTACTAGTTTTT[-/C/T]GGAGTAATTAGTTGG	55159
rs11640111	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74627152	CTGGGATGTTTCTCA[G/T]CTCAAACAAAACTTA	55159
rs11640231	snp	C/T	0.312348	0.242101	intron-variant	RFWD3	GRCh38.p7	16:74633881	CTTGAGCCCAGGAGG[C/T]GGAGGTTGTAATGAG	55159
rs11647098	snp	C/T	0.00676609	0.0577691	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621926	ggACAAGGCTTTTTT[C/T]CTTTGGAGAAATCAC	55159
rs11859709	snp	A/C	0.0182019	0.0936463	intron-variant	RFWD3	GRCh38.p7	16:74634376	ATTTTTTACTAAGTA[A/C]TTtatatatatatat	55159
rs11859900	snp	C/T	0.202035	0.245356	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621754	GCTGGAGTGCAGTGG[C/T]GCGATCTCGACTCAC	55159
rs11861764	snp	C/T	0.0205511	0.0992634	intron-variant	RFWD3	GRCh38.p7	16:74643414	GCAATCCCCTTGCCT[C/T]AGATTTTTAACAATG	55159
rs11861845	snp	C/T	0	0	intron-variant	RFWD3	GRCh38.p7	16:74643670	TGTTACTAGCAACTG[C/T]TTTTTTTTTTTTTTT	55159
rs11863463	snp	A/T	0.0414363	0.137845	intron-variant	RFWD3	GRCh38.p7	16:74666224	gatagatagatagat[A/T]gattagatacataga	55159
rs12599437	snp	A/G	0.0341408	0.126114	intron-variant	RFWD3	GRCh38.p7	16:74653353	caacaaaaaaacaaa[A/G]aaaTGACACCCAAAA	55159
rs12924948	snp	A/G	0.450483	0.149354	intron-variant	RFWD3	GRCh38.p7	16:74643699	TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC	55159
rs12925578	snp	A/T	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74635678	TGATAAATCTTTTTA[A/T]TAAAAACTTAGATGG	55159
rs12927568	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74656286	actccagcctgggca[A/G]cagagtgagaccttg	55159
rs12927569	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74656288	tccagcctgggcaac[A/C]gagtgagaccttgtc	55159
rs12927581	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74656309	agaccttgtcttgcc[A/T]aaaaaaaaaaaaaaa	55159
rs12927586	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74656328	aaaaaaaaaaaaaaa[A/G]aaagaaaaGAAAAGA	55159
rs12933037	snp	A/G	0.472241	0.114494	intron-variant	RFWD3	GRCh38.p7	16:74626276	GTAAAAAAAGTTCAT[A/G]TTTTCCCTTACCAAT	55159
rs12934735	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74641910	ccagcctgggcaaca[A/G]gagcaaaactccgtc	55159
rs12935075	snp	A/T	0.354665	0.227036	intron-variant	RFWD3	GRCh38.p7	16:74642135	CTAGTGTACCttttt[A/T]aatttgacacagagt	55159
rs16944746	snp	C/T	0.2262	0.248865	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668834	AATAAACGTAGTATT[C/T]CATTGGAAAGCCAAA	55159
rs17854996	snp	A/G	0	0	missense	RFWD3	GRCh38.p7	16:74623944	CACTCCCACTTATAG[A/G]TGTGGACCATCTTCT	55159
rs17854997	snp	C/T	0	0	missense	RFWD3	GRCh38.p7	16:74637875	ACACGCCTTTGAAGC[C/T]TAGTGCACTTATCAG	55159
rs28417898	snp	C/T	0.338296	0.233889	intron-variant	RFWD3	GRCh38.p7	16:74653704	TGACAGGTGACCTAC[C/T]AGAAGTTTTAATAAT	55159
rs28480186	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74648784	CGTCTCAAAAAAAAA[A/G]AAAAAAAAGGGGATA	55159
rs28483926	snp	A/G	0.00914312	0.0669923	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623367	CACTTGTGTGGAGAT[A/G]AGACAAGTTACTAAA	55159
rs28529414	snp	A/G			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622481	AAAATTTAAAAAAGG[A/G]AAAAATTATGTCCTA	55159
rs28561398	snp	A/G	0.00795532	0.062565	intron-variant	RFWD3	GRCh38.p7	16:74651254	CCACTTGCATAACAC[A/G]TAACATTATACTAGG	55159
rs28616016	snp	C/T	0.479177	0.0998894	intron-variant	RFWD3	GRCh38.p7	16:74643066	CGCTACAAGTGAGCA[C/T]TGGTTGGACCAAATG	55159
rs28656043	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74648785	GTCTCAAAAAAAAAG[A/G]AAAAAAAGGGGATAT	55159
rs28681530	snp	C/T	0.449599	0.150533	intron-variant	RFWD3	GRCh38.p7	16:74648598	CAGTATGGTGAAACC[C/T]CGTCTCTAACTTAAA	55159
rs28711408	snp	A/G	0.375	0.216506	downstream-variant-500B	RFWD3	GRCh38.p7	16:74620990	TTAAAAAAAAAAAAA[A/G]AAAAAAAGGCCGGGT	55159
rs28850665	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74656332	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAATA	55159
rs34154577	in-del	-/CAT	0.234401	0.249513	intron-variant, cds-indel	RFWD3	GRCh38.p7	16:74662028	TTCCATCTCTAATTC[-/CAT]CATGTTAGCGTATTC	55159
rs34166663	in-del	-/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667108	TTGCACCCGCCCCGG[-/T]AAAAAATGGGAGGTT	55159
rs34456890	in-del	-/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663976	CTAAAACAAAACACA[-/G]GAACAAAGCCCTTCT	55159
rs34516330	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74664952	GTCGGAGGTGCCTAG[-/T]AACGAGAGACCATGG	55159
rs34555719	in-del	-/C			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623333	TTGCCACAAAGCACA[-/C]CCCAGGTGTGCTATC	55159
rs34657625	in-del	-/A	0.467845	0.122652	intron-variant	RFWD3	GRCh38.p7	16:74625514	AGAAAAAAAAAAAAA[-/A]GGACAGACCAGGCGC	55159
rs34738311	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74642030	CATATATAGCTAATC[-/A]AAATACATAATAACT	55159
rs35168235	in-del	-/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664564	CAGCCTGGGCAACAC[-/G]GGCAAAACCCCGTCT	55159
rs35195621	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74626308	TTTAAGCAAAACTAC[-/T]TTTTTATATGAAAGT	55159
rs35287818	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645082	GGATACAAATGCTTA[C/G]AAGAAAACACAATGG	55159
rs35397997	in-del	-/C/TT			intron-variant	RFWD3	GRCh38.p7	16:74643670	GTTACTAGCAACTGC[-/C/TT]TTTTTTTTTTTTTTT	55159
rs35637941	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74627759	AGGACAGAGGAGTAT[-/C]CCTGTGAAAGGCAAA	55159
rs35692880	in-del	-/G			intron-variant	RFWD3	GRCh38.p7	16:74646509	AAGAATTAATTCGCT[-/G]GGGCGCAGTGGCTCA	55159
rs35791327	in-del	-/C			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662721	TAAAGGGCCTATGGG[-/C]CCTTGGTAAGGAGTT	55159
rs36009591	in-del	-/A	0.476052	0.106772	downstream-variant-500B	RFWD3	GRCh38.p7	16:74620977	GAGTGAGATTCAGTT[-/A]AAAAAAAAAAAAAAA	55159
rs36083956	snp	C/T	0.201727	0.245295	intron-variant	RFWD3	GRCh38.p7	16:74645985	GATCTCCTGACCTCG[C/T]GATCCGTCCGCCTTG	55159
rs36088150	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74666606	GGGTTCGGGCTCCTT[-/T]AGCCCCGACCACTGG	55159
rs36147760	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74638938	CTCCCAGGCTACAAA[-/A]CTTGTATAGTATGTT	55159
rs55919640	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74634640	ACGATCCTCCCGCCT[C/T]GGCCTCCCAAAGTGC	55159
rs55988216	snp	A/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662149	AAACTAAAAAAAAAA[A/T]TTTTTTTTTGTTATA	55159
rs56056110	in-del	-/TCTCTC/TCTCTCTC	0	0	intron-variant	RFWD3	GRCh38.p7	16:74631478	CTCTCTCTCTCTCTC[-/TCTCTC/TCTCTCTC]AAAAATAAATAAATA	55159
rs56099065	snp	C/T	0.448323	0.15221	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663061	AGGTGCCTGCCACCA[C/T]GCCTGGCTAATTTTT	55159
rs56143602	snp	C/T	0.46865	0.121211	intron-variant	RFWD3	GRCh38.p7	16:74660794	AGGCAAGCACTTTTA[C/T]TTCCACCTATGAGGA	55159
rs56295454	snp	A/C	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664521	TTTGGGAGACTGAGG[A/C]AGGTAGCTGGAGACC	55159
rs56803461	in-del	-/C/CT	0	0	intron-variant	RFWD3	GRCh38.p7	16:74643669	TGTTACTAGCAACTG[-/C/CT]TTTTTTTTTTTTTTT	55159
rs56890104	in-del	-/TTACCTCC			utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666845	TCGGTAGTTACCTCG[-/TTACCTCC]GCCGCACTCCGAATG	55159
rs57488599	in-del	CGCCGAAGACTCGGTAGTTACCTCC/G	0.5	0	utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666845	CTCGGTAGTTACCTC[CGCCGAAGACTCGGTAGTTACCTCC/G]GCCGCACTCCGAATG	55159
rs58136167	snp	A/G	0.361894	0.223562	intron-variant	RFWD3	GRCh38.p7	16:74666730	AATCAGGCGTGGGGA[A/G]GTTTATCCCGAAGCT	55159
rs58137570	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667080	ACAATTGGCAGGAAT[C/T]TACGTCCGTCACCTT	55159
rs58273376	in-del	-/A/AA			intron-variant	RFWD3	GRCh38.p7	16:74659601	AAAACAAAAAAAAAA[-/A/AA]CCCAGAGTAATATGC	55159
rs58439735	snp	A/G	0.00835141	0.0640778	intron-variant	RFWD3	GRCh38.p7	16:74632044	GTGCCCACTTCTAAA[A/G]GCAATATATTTTAAA	55159
rs58546865	snp	C/G	0.0696718	0.173152	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668535	TCCCTTGGCAGACGT[C/G]AAGTGAGAAAATACA	55159
rs58823246	in-del	-/AAT	0.12932	0.218944	intron-variant, cds-indel	RFWD3	GRCh38.p7	16:74662148	TAAACTAAAAAAAAA[-/AAT]TTTTTTTTGTTATAT	55159
rs58956493	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74636802	CACTGCAACCTCCAT[C/T]TCCTGGGTTCAAGCA	55159
rs59964330	in-del	-/A	0.462691	0.131387	intron-variant	RFWD3	GRCh38.p7	16:74633279	GAAAAAAAAAAAAAA[-/A]GAAAAGAAAAAAAAG	55159
rs60142178	in-del	-/AAA			intron-variant	RFWD3	GRCh38.p7	16:74637145	AAAAAAAAAAAAAAA[-/AAA]CAACTTAAAAGGAGA	55159
rs60528397	in-del	-/A			downstream-variant-500B	RFWD3	GRCh38.p7	16:74620997	AAAAAAAAAAAAAAA[-/A]GGCCGGGTGCGGTAG	55159
rs60745895	snp	C/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74657100	GTCAAGAGTAGTCTT[C/G]CAAATGGGGTTTTCC	55159
rs60843417	in-del	-/AAA/AAAA/AAAG/AAC			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664761	TAAAAAAAGAAAAAA[-/AAA/AAAA/AAAG/AAC]GAAAGAAATAAAATA	55159
rs61457427	in-del	-/AT			intron-variant	RFWD3	GRCh38.p7	16:74634398	TATATATATATATAT[-/AT]TTTGAGACAAGGCCT	55159
rs61530089	in-del	-/TATCC			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74661991	GAGCAAACTTTATCC[-/TATCC]CTTTCATTATTTTTG	55159
rs62053564	snp	A/G	0.0126979	0.078662	intron-variant	RFWD3	GRCh38.p7	16:74638125	AGAAAAATCTCTCCA[A/G]AAACAGGTTTTAGGG	55159
rs62053578	snp	A/C	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74639332	TGTGAGCTACTACAC[A/C]CAGTGCGCTAAGCCA	55159
rs62053579	snp	C/T	0	0	intron-variant	RFWD3	GRCh38.p7	16:74643671	GTTACTAGCAACTGT[C/T]TTTTTTTTTTTTTTT	55159
rs62053580	snp	A/G	0.223225	0.248562	intron-variant	RFWD3	GRCh38.p7	16:74646176	GCTCAGGAGTTTGAA[A/G]CCAGACTGGACAACA	55159
rs62053581	snp	A/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74655405	CCACCACGCCTGGCT[A/T]ATTTTTTTTTTTTTT	55159
rs62053582	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74659511	GAGGCACAAGAATCG[C/T]TTGAACCCGGGAGCC	55159
rs62053585	snp	A/T	0.499477	0.0161657	intron-variant	RFWD3	GRCh38.p7	16:74666216	GATAGATAGATAGAT[A/T]GATAGATTGATTAGA	55159
rs62053587	snp	G/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667118	CCCCGGAAAAAATGG[G/T]AGGTTTTTTTGTTTT	55159
rs66769310	snp	A/C	0.0154538	0.0865337	intron-variant	RFWD3	GRCh38.p7	16:74628816	GATAAAAATTATCAA[A/C]CCTCTCTGTAGAAAC	55159
rs67145363	in-del	-/TA	0.445328	0.156035	intron-variant	RFWD3	GRCh38.p7	16:74634379	TTTTACTAAGTACTT[-/TA]TATATATATATATAT	55159
rs67489206	in-del	-/TATCC	0.00874735	0.0655527	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74661986	AGGCTGAGCAAACTT[-/TATCC]TATCCCTTTCATTAT	55159
rs67943734	in-del	-/T	0.481165	0.0951993	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667146	TTTTTTTTTTTTTTT[-/T]AGCGCGTTTTATTTG	55159
rs71158533	in-del	-/AA	0	0	intron-variant	RFWD3	GRCh38.p7	16:74641953	AAAAAAAAAAAAAAA[-/AA]CCAAAGAAACCAAAA	55159
rs71158534	in-del	-/A	0	0	intron-variant	RFWD3	GRCh38.p7	16:74656331	AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAT	55159
rs71376286	in-del	-/CT/CTCTCGCTCT/CTCTCT/CTCTCTCT/CTCTCTCTCT	0.0142736	0.0832652	intron-variant	RFWD3	GRCh38.p7	16:74631463	GGTGACAGAGTGAGA[lengthTooLong]CTCTCTCTCTCTCTC	55159
rs71376287	in-del	-/A	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74632088	ACACAGTCTCAGACC[-/A]AAAAAAACAGAGCTA	55159
rs71376289	in-del	-/A	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74637613	ACTCCAGCCTAGGTG[-/A]CAGAGTGAGACTCTG	55159
rs71376290	multinucleotide-polymorphism	AA/CT	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74639002	ATGGTATTTATGTAT[AA/CT]AAACATAGAAAAGGT	55159
rs71376292	in-del	-/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74639166	CCTCAGCCTCCCAAG[-/T]AGCTGAGATGACCGG	55159
rs71376293	in-del	-/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74645746	GTCACAAATATTTTC[-/T]TTTTTTTTTTTTTTT	55159
rs71376294	in-del	-/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74646508	AAAGAATTAATTCGC[-/T]TGGGCGCAGTGGCTC	55159
rs71376295	in-del	-/CAACAACAACAA	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74646904	GGTGAAACCCCGTCT[-/CAACAACAACAA]CAACAACAACAACAA	55159
rs71376296	in-del	-/T	0.448323	0.15221	intron-variant	RFWD3	GRCh38.p7	16:74650998	CCCTTTATTTACTAG[-/T]TTTTTGGAGTAATTA	55159
rs71376297	in-del	-/TT	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74657479	CAGGTTTTCTTTTTC[-/TT]TTTTTTTTTTTTTTT	55159
rs71682116	in-del	-/A	0.327914	0.237549	intron-variant	RFWD3	GRCh38.p7	16:74644824	AATTAACAGAAGTGC[-/A]AAAAAAATGATACAA	55159
rs72792716	snp	C/T	0.154661	0.231107	intron-variant	RFWD3	GRCh38.p7	16:74645418	GTCTTTAGGCGATTT[C/T]GTCATTGAATGATCC	55159
rs72792719	snp	A/G	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74646354	GCACTCCAGCATGAG[A/G]GACAGAATGAGACCC	55159
rs72792720	snp	C/T	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74647652	GCTAGAGCGCAGTGA[C/T]GCTATTTGGGCTCAC	55159
rs72792722	snp	A/G	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74652626	TAAAATTTAAATAAT[A/G]TTAGTTTTAAGATAA	55159
rs72792723	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662821	TGGGAGTCCAGACCA[A/G]AGGTCAGAGAGACCT	55159
rs73612432	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74654379	TTTGTTCCTCTGTTA[C/T]TTAGGAGTGTGTTAT	55159
rs74024516	snp	A/G	0.0356815	0.128715	intron-variant	RFWD3	GRCh38.p7	16:74631133	ACTCCTTTAAATTCC[A/G]TAACATTTGTTTTGG	55159
rs74250243	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74655839	CCTATGTCTGTGCTC[G/T]CTAAATGGAACTACA	55159
rs74356644	snp	G/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74641179	ATTTTTTTTTTTTTT[G/T]AAGACAGAGTTTCGC	55159
rs74382120	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74641690	AGCACTTTGGGAGTC[A/C]AAGGCAGGCTGATCA	55159
rs74384473	in-del	-/AA			intron-variant	RFWD3	GRCh38.p7	16:74635482	AAAAGAAAAAAAAAA[-/AA]TCAACAAGGTAACAG	55159
rs74397590	snp	C/T	0.335101	0.23507	intron-variant	RFWD3	GRCh38.p7	16:74665756	TTTCTTTCTTTCTTT[C/T]TTTTTTTGAGATGGA	55159
rs74566592	snp	A/G	0.0379877	0.132479	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622509	CTAAAATATTAAAGG[A/G]TCATTAAAAGGCACA	55159
rs74603142	snp	C/T	0.0124432	0.0778894	synonymous-codon	RFWD3	GRCh38.p7	16:74637874	AACACGCCTTTGAAG[C/T]CTAGTGCACTTATCA	55159
rs74613721	snp	C/T	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663674	ATAAATTAACCAGGA[C/T]GACACAAATGCAAAC	55159
rs74691006	snp	C/T	0.00874735	0.0655527	intron-variant	RFWD3	GRCh38.p7	16:74654171	GTCATGTCCTCTCTT[C/T]CATTCTTCATTTTAG	55159
rs74820302	snp	A/T	0.281577	0.247998	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664354	TACTCAAGAGACATT[A/T]AGCAACTCAGCCTTC	55159
rs74846166	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74627643	AGGGAAATGAACTAG[A/G]CACAGTTCAGACAAG	55159
rs74894553	snp	A/G	0.5	0	downstream-variant-500B	RFWD3	GRCh38.p7	16:74620988	AGTTAAAAAAAAAAA[A/G]AAAAAAAAAGGCCGG	55159
rs74935278	snp	C/T	0.00914312	0.0669923	intron-variant	RFWD3	GRCh38.p7	16:74658724	ACTGACATCTTTCAA[C/T]ATTTAAATTCTGTAT	55159
rs75007821	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74652553	TATTTTGGAGTACAG[C/T]ACAGGGTCTGGCTTC	55159
rs75096056	snp	C/T	0.202035	0.245356	intron-variant	RFWD3	GRCh38.p7	16:74625545	ACAGACCAGGCGCAA[C/T]GGCTCACGCCTATAA	55159
rs75128674	snp	A/G	0.363359	0.222822	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667119	CCCGGAAAAAATGGG[A/G]GGTTTTTTTGTTTTT	55159
rs75177685	snp	C/G	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74646408	CATGATTTATATAAA[C/G]AAAAAAAATATTATT	55159
rs75203104	snp	A/G	0.201727	0.245295	intron-variant	RFWD3	GRCh38.p7	16:74654542	TCCCTGAGACAAAAC[A/G]ATACTGAAATTAGGC	55159
rs75355556	snp	C/G	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74665144	AAGAGGTGGGCGGGG[C/G]AAGTGTTCAAATCTT	55159
rs75459913	snp	A/T	0.114387	0.210022	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668081	TTATTAACTAGGGAA[A/T]CTACAAGAGGGTCAA	55159
rs75551490	snp	A/G	0.202035	0.245356	intron-variant	RFWD3	GRCh38.p7	16:74647779	GCATTTTTACTAGGG[A/G]TGGGGTTTCGCCATG	55159
rs75647170	snp	A/G	0.0517044	0.152246	intron-variant	RFWD3	GRCh38.p7	16:74656213	TGAGGCAGGAGGATC[A/G]AGGATCACCTGAGCC	55159
rs75647437	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74641689	CAGCACTTTGGGAGT[A/C]CAAGGCAGGCTGATC	55159
rs75659996	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668075	CAGGCATTATTAACT[A/G]GGGAATCTACAAGAG	55159
rs75820229	snp	C/T	0.0422008	0.138995	intron-variant	RFWD3	GRCh38.p7	16:74648883	TTGAGCCCAGGAGTT[C/T]GAAACCAACTGGGTA	55159
rs75932415	in-del	-/AA			intron-variant	RFWD3	GRCh38.p7	16:74629676	CCAACAAAAAAAAAA[-/AA]CCTTGCCATATTTTA	55159
rs75946276	snp	G/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74658783	TTTTTTTTTTTTTTT[G/T]TGAGACAGAGAGTCA	55159
rs75949332	snp	A/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74658768	AGCAGATTCTATAAT[A/T]TTTTTTTTTTTTTTT	55159
rs76020499	snp	C/T	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74636094	TATATCAGTAACCTA[C/T]ACTTCCAAGGACCTC	55159
rs76065543	snp	C/T	0.181659	0.240478	intron-variant	RFWD3	GRCh38.p7	16:74644165	TCTACATAAGGCAAA[C/T]GATGCAGACTTCCTT	55159
rs76072873	snp	A/G	0.5	0	downstream-variant-500B	RFWD3	GRCh38.p7	16:74620987	CAGTTAAAAAAAAAA[A/G]AAAAAAAAAAGGCCG	55159
rs76140562	snp	G/T	0.0111196	0.0737302	intron-variant	RFWD3	GRCh38.p7	16:74657894	CATTTCATAAGAAGA[G/T]TTAATCAAATACATA	55159
rs76155630	snp	C/T	0.00534136	0.0514018	missense	RFWD3	GRCh38.p7	16:74649149	GTTTGGGGAGGGTCT[C/T]GCCTCCATCGATACA	55159
rs76158642	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74647708	GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATCCC	55159
rs76197436	snp	G/T	0.317451	0.240729	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667130	TGGGAGGTTTTTTTG[G/T]TTTTTTTTTGTTTGG	55159
rs76327540	snp	A/T	0.195214	0.243923	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663774	GAGCCAAAAGATAAA[A/T]CTCAAAGCCTGCAAA	55159
rs76362288	snp	C/T	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74654321	TCATTTATTTATATG[C/T]TAACCTTTATTATTT	55159
rs76374477	snp	A/T	0	0	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667114	CCCGCCCCGGAAAAA[A/T]TGGGAGGTTTTTTTG	55159
rs76490805	snp	A/G	0.0232847	0.105357	intron-variant	RFWD3	GRCh38.p7	16:74665104	CACAACAGGCAGGAC[A/G]AAAGCCCCTCAATTA	55159
rs76497052	snp	A/G	0.0432226	0.14051	intron-variant	RFWD3	GRCh38.p7	16:74638013	GGGATTAGGAAGGCT[A/G]CAGAAGACTTCCCAT	55159
rs76634113	snp	A/T	0.00667815	0.0573975	intron-variant	RFWD3	GRCh38.p7	16:74638022	AAGGCTACAGAAGAC[A/T]TCCCATCCAGGTGGC	55159
rs76646536	snp	G/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74650369	TTTTTTTTTTTTTTG[G/T]CAATGGGGGTGGGGG	55159
rs76719803	snp	G/T	0.0111196	0.0737302	intron-variant	RFWD3	GRCh38.p7	16:74630362	CTCGTCTTCCCAAAG[G/T]GCTGGGATTACAGGC	55159
rs76830516	snp	G/T	0.0260105	0.111035	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622951	AGGAACTCTCAAAAT[G/T]GGAGACAAGTTCTTC	55159
rs76938680	snp	A/G	0.202651	0.245475	intron-variant	RFWD3	GRCh38.p7	16:74648837	ATGACTACAATCTCA[A/G]TGGTTTGGGAGGCCG	55159
rs77132945	snp	A/G	0.0384357	0.133196	missense	RFWD3	GRCh38.p7	16:74637968	TGTTCCTTCAGTAGG[A/G]AACTAGAGGGGGAAA	55159
rs77153870	snp	G/T	0	0	intron-variant	RFWD3	GRCh38.p7	16:74650367	GCTTTTTTTTTTTTT[G/T]GGCAATGGGGGTGGG	55159
rs77174647	snp	C/G	0.195214	0.243923	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667029	TGGCTGGTAGTTCGT[C/G]CTGACGAGGCGGGAC	55159
rs77288344	snp	C/G	0.189576	0.242588	intron-variant	RFWD3	GRCh38.p7	16:74629965	TTCTCAATCTCATAA[C/G]TGGATTAAATGATAA	55159
rs77312640	snp	G/T	0	0	intron-variant	RFWD3	GRCh38.p7	16:74640160	ATTTTTTTTTTTTTT[G/T]TTGAAACAGTCTTGC	55159
rs77457049	snp	A/G	0.030278	0.119257	intron-variant	RFWD3	GRCh38.p7	16:74649104	ATAAATAAATAAATA[A/G]ATTTTTTTAAAATGA	55159
rs77635293	snp	A/G	0.0267878	0.112589	intron-variant	RFWD3	GRCh38.p7	16:74654111	TTTGTCACACCTAAA[A/G]GGGACCCTGTATCCA	55159
rs77652772	snp	A/G	0.0260105	0.111035	intron-variant	RFWD3	GRCh38.p7	16:74626263	TATATGAGCTTCTGT[A/G]AAAAAAGTTCATGTT	55159
rs77676738	snp	A/C	0	0	intron-variant	RFWD3	GRCh38.p7	16:74641932	AACTCCGTCTCCAAA[A/C]AAAAAAAAAAAAAAA	55159
rs77829084	snp	C/T	0.0314385	0.121371	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668452	AAAGGAGCTGCAGGC[C/T]GGCCATTAGAACTCA	55159
rs77859775	snp	C/T	0.0138799	0.0821421	intron-variant	RFWD3	GRCh38.p7	16:74638243	TCTAGTGTTCAGCTA[C/T]GGCAAATTGTAAAAG	55159
rs78063477	snp	A/G	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74634816	AGAGAGGAAAAAAAA[A/G]GGGGGGAAGGGGGGC	55159
rs78148391	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622002	CTAATGCAAGGACTG[A/G]TAAGACTTAAGATTC	55159
rs78199625	snp	A/C	0.0298908	0.118541	intron-variant	RFWD3	GRCh38.p7	16:74627840	GTTTATAGCCACTCT[A/C]CTGACAGAGACCTCA	55159
rs78201989	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74626207	ACATACACACATATG[C/T]GGATATGTGGGATTA	55159
rs78219119	snp	C/T	0.201727	0.245295	intron-variant	RFWD3	GRCh38.p7	16:74626287	TCATGTTTTCCCTTA[C/T]CAATATTTTAAGCAA	55159
rs78227885	snp	A/G	0.178144	0.239451	intron-variant	RFWD3	GRCh38.p7	16:74640110	CCTTGTGGCTAAGGG[A/G]GGACTACTGTAGCCC	55159
rs78254155	snp	A/C/G	0.0197687	0.0974348	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623025	TATGTCTTTTCTCCT[A/C/G]ATCTCTGACACTAGG	55159
rs78385317	snp	A/C	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74633985	ACTAGATCTTCTGTC[A/C]AAAAAAAAAAAAATT	55159
rs78397050	snp	A/G	0.137867	0.223442	intron-variant	RFWD3	GRCh38.p7	16:74666082	GGAAGAGGAGGGAGA[A/G]GGAGACGGGAGGGGA	55159
rs78428634	snp	C/T	0.0126979	0.078662	intron-variant	RFWD3	GRCh38.p7	16:74659032	CTCAAAGTTCTGAGA[C/T]TACAGGCGTGAGCCA	55159
rs78484755	snp	A/C	0.203575	0.245652	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621281	GATTCCGTCTCAAAA[A/C]ACAAACAAACGAACA	55159
rs78536679	snp	A/C	0	0	intron-variant	RFWD3	GRCh38.p7	16:74633984	AACTAGATCTTCTGT[A/C]AAAAAAAAAAAAAAT	55159
rs78639647	snp	C/G	0.20111	0.245173	intron-variant	RFWD3	GRCh38.p7	16:74638170	TGGTCAGGAATTTGA[C/G]TATTACTAGAAAATG	55159
rs78664779	snp	A/T	0.0271762	0.113356	intron-variant	RFWD3	GRCh38.p7	16:74642017	ATAATTTACAAATAC[A/T]TATATAGCTAATCAA	55159
rs78665999	snp	C/G	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74624199	GCAAAGCAGGCTGTC[C/G]CTAACCTTTGCAAGG	55159
rs78702653	snp	A/C	0.0267878	0.112589	intron-variant	RFWD3	GRCh38.p7	16:74661915	AGGACATTTTTTACA[A/C]TTGCAAAATTAACTG	55159
rs78754429	snp	G/T	0.324619	0.238604	intron-variant	RFWD3	GRCh38.p7	16:74653151	CGAGACCAGCCTGAT[G/T]AACATGGTGAAACCC	55159
rs78796563	snp	A/G	0.0373272	0.131416	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630800	CTTTCTGAGCTACTA[A/G]CTCCTGCACATGACT	55159
rs78856184	snp	C/T	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74651016	TTTGGAGTAATTAGT[C/T]GGGGTTCTAACAACT	55159
rs78877531	snp	A/G			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664751	AAGACTCCGTCTAAA[A/G]AAAGAAAAAAGAAAG	55159
rs78888132	snp	C/G	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74654610	TTAAGGGAAGAGTCA[C/G]GCATCTCTCACTTTA	55159
rs78889637	snp	C/T	0.0383715	0.133092	intron-variant	RFWD3	GRCh38.p7	16:74633928	CCCTGCATTCCAGCC[C/T]GGGAGATCACACCCC	55159
rs78946503	snp	A/G	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74650924	AAACCCACTTCATCA[A/G]CTATCTGATTGTCCA	55159
rs78994915	snp	G/T	0.5	0	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662920	TTCTTTTTTTTTTTT[G/T]TTGAGATGGAGTCTC	55159
rs79021677	snp	G/T	0.0263992	0.111815	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623051	CTAGGGGAGACTCAA[G/T]TAAAAGCTTTGACCT	55159
rs79094754	snp	G/T	0.5	0	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662923	TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCGCT	55159
rs79190158	snp	G/T	0.117188	0.211804	intron-variant	RFWD3	GRCh38.p7	16:74630345	CCTCCTGATCTGTCC[G/T]CCTCGTCTTCCCAAA	55159
rs79197706	snp	C/T	0.0260105	0.111035	intron-variant	RFWD3	GRCh38.p7	16:74657940	TGACACGTATATCAA[C/T]AGAATTCTACATAGA	55159
rs79233910	snp	A/C	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74656313	CTTGTCTTGCCAAAA[A/C]AAAAAAAAAAAAAAA	55159
rs79235318	snp	A/G	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74625515	CGAGACCGTCTCAAG[A/G]AAAAAAAAAAAAGGA	55159
rs79268670	in-del	-/AATT			intron-variant	RFWD3	GRCh38.p7	16:74641473	TGGCCTAAACAGATT[-/AATT]TTGACTAGAGAACTA	55159
rs79274416	snp	C/T	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74654096	TGGTTCCAAAACATT[C/T]TTGTCACACCTAAAA	55159
rs79282954	snp	A/T	0.111928	0.208413	intron-variant	RFWD3	GRCh38.p7	16:74644260	ATCCCAAGTCACAGG[A/T]CAAGTAAAACCTCAC	55159
rs79323247	snp	G/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74658785	TTTTTTTTTTTTTTT[G/T]AGACAGAGAGTCACT	55159
rs79333582	snp	C/T	0.195214	0.243923	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663340	GCCAGTTAAGGAAGA[C/T]TATAAAGTAGGAGGA	55159
rs79426032	snp	C/T	0.0260105	0.111035	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667831	CAGCAACAATTTCTT[C/T]TTCAGCAGAAAATAC	55159
rs79452330	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664755	CTCCGTCTAAAAAAA[A/G]AAAAAAGAAAGAAAT	55159
rs79470274	snp	A/C	0.20111	0.245173	intron-variant	RFWD3	GRCh38.p7	16:74660833	TCAGAAGTTACCTGA[A/C]TTGCCAAAAGTCACA	55159
rs79477071	snp	C/G	0.200182	0.244986	intron-variant	RFWD3	GRCh38.p7	16:74656164	TTAGCTGGGTGTGGC[C/G]GCTTGTGCCTTTAGT	55159
rs79862626	snp	A/C	0	0	intron-variant	RFWD3	GRCh38.p7	16:74647087	GCGACACTCGTCTCA[A/C]AAAAAAAAAAAGATT	55159
rs79947864	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656990	TTCCTTTCCTTCTTA[C/T]TGGTTAGTTTATTGC	55159
rs80023345	snp	A/G	0.192715	0.243348	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667480	GGGATCTGAGCTACT[A/G]AACAGTCTCAAATCA	55159
rs80043761	snp	A/G/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74638218	AGGCAAAACGAGAGA[A/G/T]CAGAGCTAATCTAGT	55159
rs80079199	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650175	GAGATATTCCCTTCA[C/G]AATATGTTAAATTTC	55159
rs80109295	snp	A/C	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74641931	AAACTCCGTCTCCAA[A/C]AAAAAAAAAAAAAAA	55159
rs80318375	snp	C/T	0.202035	0.245356	intron-variant	RFWD3	GRCh38.p7	16:74634548	TGCCACCACACCAAG[C/T]TAGTTAAGAAAAATT	55159
rs80341691	snp	A/G	0.0134861	0.0810011	intron-variant	RFWD3	GRCh38.p7	16:74654585	CTACAATGGCCTCTA[A/G]GTGTTCAAATTAAGG	55159
rs111237674	snp	A/G	0.0236746	0.106192	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667769	GCTGTATGAGAAATA[A/G]CTTTTGAAACTGAGG	55159
rs111271608	snp	G/T	0.0410537	0.137264	intron-variant	RFWD3	GRCh38.p7	16:74642398	CAGAGTGCTAGGATT[G/T]CAGGTGTGAGCCACT	55159
rs111322001	snp	A/G	0.196149	0.244131	intron-variant	RFWD3	GRCh38.p7	16:74665685	GGATCCCTGGGGCCC[A/G]GGAGTTCGAGACTGC	55159
rs111409089	snp	C/T	0.0189856	0.0955633	intron-variant	RFWD3	GRCh38.p7	16:74639963	AGTATACTGGTATAA[C/T]TGCTCTATTTTATTA	55159
rs111459164	snp	C/T	0.0839998	0.186933	intron-variant	RFWD3	GRCh38.p7	16:74637501	GCATGGTGGTGGGCT[C/T]CTGTAATCCCAGCAC	55159
rs111485514	snp	G/T	0	0	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664542	GCTGGAGACCAGGAG[G/T]TGGAGACCAGCCTGG	55159
rs111513241	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74641612	AAGTTATAATCTAAC[A/G]TAACATTTGCATACA	55159
rs111547357	snp	A/G	0.00557542	0.0525036	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667957	GGGAGTAAAGACTCC[A/G]GTAACCCTCAAGCAA	55159
rs111581866	snp	G/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662159	AAAAAATTTTTTTTT[G/T]TTATATAGATGAAGG	55159
rs111667788	snp	A/G	0.123798	0.215808	intron-variant	RFWD3	GRCh38.p7	16:74648854	GGTTTGGGAGGCCGA[A/G]GCAGGACGATACCTT	55159
rs111753759	snp	C/T	0.5	0	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667871	TGGAAGTAATGATTC[C/T]GACAGATATGGTGAA	55159
rs111759686	in-del	-/ATTT	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74649366	AGGTACCATCAGTGA[-/ATTT]ATTTTTAAAAATTTA	55159
rs111816593	snp	A/T	0.182296	0.240658	intron-variant	RFWD3	GRCh38.p7	16:74626818	TTAAGAGAAAAACAA[A/T]TCTGTGAGTTGTCTG	55159
rs111911076	snp	C/T	0.0107246	0.0724382	intron-variant	RFWD3	GRCh38.p7	16:74652930	AAATGATCCACCCAC[C/T]TTGGCCTCCCAAAAT	55159
rs111911320	snp	C/T	0.0452528	0.143452	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74662943	GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG	55159
rs112031472	snp	C/T	0.5	0	missense, intron-variant	RFWD3	GRCh38.p7	16:74630821	GCACATGACTGCTCG[C/T]GTTTCGCACGTCATA	55159
rs112049165	snp	A/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74631459	GCCTGGGTGACAGAG[A/T]GAGACTCTCTCTCTC	55159
rs112054128	snp	G/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74653182	CATCTCTACAAAAAA[G/T]ACACAATATAGCCAG	55159
rs112107021	snp	C/T	0.201727	0.245295	intron-variant	RFWD3	GRCh38.p7	16:74655388	GGGACTACAGGCACC[C/T]GCCACCACGCCTGGC	55159
rs112110959	snp	A/C/G/T			intron-variant	RFWD3	GRCh38.p7	16:74626823	AGAAAAACAATTCTG[A/C/G/T]GAGTTGTCTGTTTTA	55159
rs112167082	snp	C/T	0.181978	0.240568	intron-variant	RFWD3	GRCh38.p7	16:74641810	AGGCGCCTGTAATCC[C/T]GGCTACTTGGGAGAC	55159
rs112214347	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74635331	AATTAACTAGGCATG[A/G]TGGCATGCACCCGTA	55159
rs112308457	snp	A/G	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74627976	AGTCTGCTGTTATGC[A/G]TTCCACCTCTGATTC	55159
rs112394737	snp	C/G	0.109461	0.206758	intron-variant	RFWD3	GRCh38.p7	16:74625241	AGAAAAAAAAAGGTA[C/G]AGAGCACGGTGGCTC	55159
rs112411226	snp	C/T	0.5	0	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622403	GCTGAGGTGGGAGGA[C/T]TGCTTGAGGCCAGGA	55159
rs112441151	snp	C/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74657478	CCAGGTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	55159
rs112457911	snp	C/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74657977	TAAAAAAGTGATAGA[C/T]GATTAAAAAAAATCA	55159
rs112542876	in-del	-/TAGATAGA	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74666183	ATTAGATAGACAGAT[-/TAGATAGA]TAGATAGATAGATAG	55159
rs112554305	snp	C/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74645749	ACAAATATTTTCTTT[C/T]TTTTTTTTTTTTTTT	55159
rs112592739	snp	A/G	0.0425829	0.139564	intron-variant	RFWD3	GRCh38.p7	16:74641221	AAGCAGGAGTGCAAT[A/G]GTGCGACCTCGGCTC	55159
rs112884973	snp	A/G	0.081446	0.184634	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621844	GGACTACAGGCATGC[A/G]CACCACTGCACCCAG	55159
rs112942529	snp	C/T	0.5	0	missense	RFWD3	GRCh38.p7	16:74651983	CATACTCTGCAGAGC[C/T]GTCACTGTCAGAATC	55159
rs112958097	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74639252	CATGTTGCCCAGGCT[A/G]GTCTCAAACTCCTGG	55159
rs113144514	snp	A/G	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74637785	TTGTTTCTGAGATGA[A/G]CATAACTAACATTAG	55159
rs113241796	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74645606	GATCCGCCCGCCTTG[A/G]TCTCCCAAAGTGCTG	55159
rs113298747	snp	A/G	0.200182	0.244986	intron-variant	RFWD3	GRCh38.p7	16:74655284	TCACTTTGTCGCCCA[A/G]GTTAGAGTGCAGTGG	55159
rs113315839	snp	C/G	0.133093	0.220981	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663121	GTGTTAGCCAGGATG[C/G]TCTCGATCCCCTGAC	55159
rs113341244	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630591	CAGAACTCTCCATCA[C/T]ATGAAATAGCATGAA	55159
rs113477186	snp	C/G	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74633579	TGTAGTGACAAAAAG[C/G]AGTGACTGCTGGGGA	55159
rs113507850	snp	C/T	0.121446	0.214667	intron-variant	RFWD3	GRCh38.p7	16:74657559	CGGCTCACTGCAACA[C/T]CCACCTCCCGGGTTC	55159
rs113552497	snp	A/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74626332	TGAAAGTAAAAAAGT[A/T]ACAGGCTCACCAGGG	55159
rs113583772	snp	A/T	0.5	0	intron-variant	RFWD3	GRCh38.p7	16:74640055	TAAGAAAAAACATAC[A/T]ACGGTTTCAGGCATT	55159
rs113598490	snp	C/T	0.202035	0.245356	intron-variant	RFWD3	GRCh38.p7	16:74625251	AGGTAGAGAGCACGG[C/T]GGCTCATGCTTGTAA	55159
rs113755607	snp	C/T	0.5	0	missense	RFWD3	GRCh38.p7	16:74636576	GTAAGTTTTTGCAAG[C/T]CCTAAAATGAAAAAG	55159
rs113761295	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74643965	TACAGGCGTGAGCCA[C/T]CATGCCCGGCCCTAG	55159
rs113778470	snp	A/G	0	0	intron-variant	RFWD3	GRCh38.p7	16:74652556	TTTGGAGTACAGTAC[A/G]GGGTCTGGCTTCTGT	55159
rs113841907	snp	G/T	0	0	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621696	CAGGGTTTTTTTTTG[G/T]TTGTTTGTTTTTTTT	55159
rs113889232	snp	A/G	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74637582	AGGTTGCAGTGAGCC[A/G]AGATCACATCACTGC	55159
rs113940212	snp	A/G	0.00517822	0.0506191	intron-variant	RFWD3	GRCh38.p7	16:74625553	GGCGCAATGGCTCAC[A/G]CCTATAATCCAACCT	55159
rs113977258	snp	C/T	0.5	0	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623866	GGATCTTGCTTGGGG[C/T]TGCTAGGCGCTAGCA	55159
rs114040479	snp	A/C	0.0168055	0.0901129	intron-variant	RFWD3	GRCh38.p7	16:74635987	TATTAAATTTTGTTT[A/C]ACCTTGAATTAACCC	55159
rs114103855	snp	C/T	0.0168055	0.0901129	intron-variant	RFWD3	GRCh38.p7	16:74660323	TTAGGTGTGGTGGCA[C/T]GCGCCTGTAATGCCA	55159
rs114153097	snp	A/C	0.0209421	0.100162	intron-variant	RFWD3	GRCh38.p7	16:74648046	TGACCTCCCAGGCTC[A/C]AGTAATCCTGTCTCA	55159
rs114245936	snp	C/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662907	AGAATGGTCATGCTT[C/T]TTTTTTTTTTTTTTT	55159
rs114276022	snp	A/G	0.0182019	0.0936463	intron-variant	RFWD3	GRCh38.p7	16:74650098	ACATTTTATGTAAGT[A/G]GAATCATAAACTATG	55159
rs114317482	snp	C/G	0.0622301	0.165053	intron-variant	RFWD3	GRCh38.p7	16:74660010	CAGTGAGCTGTGATT[C/G]CACCACTGCACTCCA	55159
rs114735721	snp	A/T	0.0182019	0.0936463	intron-variant	RFWD3	GRCh38.p7	16:74638663	AAAACAATTACAGTT[A/T]AGCAACGCTGCTGGA	55159
rs114769691	snp	A/G	0.0209421	0.100162	intron-variant	RFWD3	GRCh38.p7	16:74648071	GTCTCAGACTCCCTA[A/G]GTAGCTAGGACTATA	55159
rs114864071	snp	A/G	0.00716266	0.059414	intron-variant	RFWD3	GRCh38.p7	16:74625796	TTAAAATTAAACATT[A/G]AGTTCTTCCTTGGCA	55159
rs114889255	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664411	AAAAAGAGCAGAATC[C/T]AGGGGGCCGCACTGT	55159
rs114941330	snp	A/G	0.0123036	0.0774623	intron-variant	RFWD3	GRCh38.p7	16:74634051	GTATTACATATGTTA[A/G]AAGTCATCAAATTGT	55159
rs114992852	snp	A/G	0.0197687	0.0974348	intron-variant	RFWD3	GRCh38.p7	16:74658320	TGACCCCCACTGCCA[A/G]AATGAAACCGCCCCA	55159
rs115079656	snp	G/T	0.0130921	0.0798413	intron-variant	RFWD3	GRCh38.p7	16:74660880	GGCAGAGCCTCAGTT[G/T]CATAATTTCTAGTAC	55159
rs115213852	snp	A/G	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74657137	CCACCAACAGGTCAT[A/G]TAAAGATAATTCTCT	55159
rs115245680	snp	A/G	0.0123036	0.0774623	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662627	CTGGCTATGCAAAGA[A/G]CCAAGAAGAGTCTCA	55159
rs115358914	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666946	TGGACAGAAGCCCTA[C/T]GCTGTGGCCAATACC	55159
rs115394738	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74638698	AGACCAAAAAAATTA[G/T]ATCAACAGCAGTCCT	55159
rs115395367	snp	C/T	0.0322114	0.122752	intron-variant	RFWD3	GRCh38.p7	16:74657763	ACAGGTGTGAGCCAC[C/T]GCGCCTAGCCAGGTT	55159
rs115429000	snp	C/T	0.0681886	0.171594	intron-variant	RFWD3	GRCh38.p7	16:74665707	CGAGACTGCAGTGAG[C/T]TCTTCCAGCCTGGGT	55159
rs115487663	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658139	AATTCTCCTCCTTCC[C/T]TGCACTTACCAACTT	55159
rs115699943	snp	A/G	0.0652144	0.168387	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621636	AGAAGACTAAAGCCT[A/G]GATTTATAAATGTGA	55159
rs116137088	snp	A/C	0.0236746	0.106192	intron-variant	RFWD3	GRCh38.p7	16:74653129	AAACTGCTTGTGCCT[A/C]GGAGTTCGAGACCAG	55159
rs116170072	snp	A/G	0.00755907	0.0610114	intron-variant	RFWD3	GRCh38.p7	16:74666267	GTTCTTTTACTACAT[A/G]GGGAAACTTTGGGCG	55159
rs116205348	snp	A/G	0.0185938	0.0946107	intron-variant	RFWD3	GRCh38.p7	16:74638033	AGACTTCCCATCCAG[A/G]TGGCAGAGTTAAGTT	55159
rs116512542	snp	C/T	0.201727	0.245295	intron-variant	RFWD3	GRCh38.p7	16:74634635	CCCAAACGATCCTCC[C/T]GCCTTGGCCTCCCAA	55159
rs116562911	snp	C/T	0.0158469	0.0875917	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662549	CCAACTAAGACACAA[C/T]TGTGAGGGAAGTACT	55159
rs116619071	snp	C/T	0.0185938	0.0946107	intron-variant	RFWD3	GRCh38.p7	16:74658979	TCACCATGTTGGCCT[C/T]GAACTCCTGGCCTAA	55159
rs116661839	snp	A/C	0.0329836	0.124112	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623350	CCAGGTGTGCTATCA[A/C]ACACTTGTGTGGAGA	55159
rs116713598	snp	C/G	0.0130921	0.0798413	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667457	TCTTCAATCTCAAAC[C/G]GCTGCAAGGGATCTG	55159
rs116923498	snp	A/G	0.0126979	0.078662	intron-variant	RFWD3	GRCh38.p7	16:74654755	TTCTGAAGAAAATTA[A/G]GCGCTACAACAGCGA	55159
rs117063429	snp	C/G	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74633271	AACCAGAGCAAAACT[C/G]CGTCTCAGAAAAAAA	55159
rs117068980	snp	A/G	0.0252325	0.109451	intron-variant	RFWD3	GRCh38.p7	16:74658863	AGCTCCGCCTCCTAG[A/G]TTCAAGGAATTCTCA	55159
rs117105077	snp	C/T	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74653226	CTCCTGTAGTTCCAG[C/T]TACTTGGGAGGCCAA	55159
rs117107958	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643987	CGGCCCTAGCAACTG[C/T]TTTGTGCTTCCGAAA	55159
rs117253733	snp	A/C	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74635929	TTTACTCCCTAAATT[A/C]TCTTATTTGGAAATT	55159
rs117287129	snp	C/T	0.00835141	0.0640778	intron-variant	RFWD3	GRCh38.p7	16:74629058	CCAAGTTGTAGTTGA[C/T]AGACCCCACAATTAA	55159
rs117290951	snp	C/T	0.0314385	0.121371	intron-variant	RFWD3	GRCh38.p7	16:74629978	AACTGGATTAAATGA[C/T]AAATAATAATAATAT	55159
rs117325386	snp	C/T	0.0271762	0.113356	intron-variant	RFWD3	GRCh38.p7	16:74664992	CCCAAACCTTGAGGA[C/T]GTCACACAAACGCTG	55159
rs117325877	snp	C/T	0.00755907	0.0610114	intron-variant	RFWD3	GRCh38.p7	16:74657359	ATTTGGTCAGTTTCC[C/T]GAATTATGAAAAAGT	55159
rs117340540	snp	C/T	0.0314385	0.121371	intron-variant	RFWD3	GRCh38.p7	16:74625215	AAAAAAAAAAAAAAG[C/T]AGAGAGGGACAGAAA	55159
rs117357621	snp	A/G	0.0318674	0.12214	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623885	TAGGCGCTAGCAAAC[A/G]ACATCTAACCAGCAG	55159
rs117420568	snp	C/G	0.320096	0.239972	intron-variant	RFWD3	GRCh38.p7	16:74646794	AGAACAAGATGAGAC[C/G]AGGCATGGTGGCTCA	55159
rs117430694	snp	C/T	0.0314385	0.121371	intron-variant	RFWD3	GRCh38.p7	16:74631734	ACCAGGAGTAAACAG[C/T]ACCAACCTGGTATGG	55159
rs117434470	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662600	GGCTGAGGCATGAAG[A/G]ATTAAAAGCAGCTGG	55159
rs117530522	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74646631	TCTCTACTAAAATAC[A/G]AAAAATTAGCCAGGC	55159
rs117556757	snp	A/G	0.0256215	0.110247	intron-variant	RFWD3	GRCh38.p7	16:74633929	CCTGCATTCCAGCCC[A/G]GGAGATCACACCCCT	55159
rs117584672	snp	C/T	0.00953873	0.0683987	intron-variant	RFWD3	GRCh38.p7	16:74656933	AAACAGCAAGAGAAC[C/T]AGACTTAGAAGATGT	55159
rs117776886	snp	C/T	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74639161	TCTTGCCTCAGCCTC[C/T]CAAGTAGCTGAGATG	55159
rs117959481	snp	C/T	0.00874735	0.0655527	intron-variant	RFWD3	GRCh38.p7	16:74628123	GAGGCAGGCAGAAGA[C/T]ACGAAAGTGATCTCA	55159
rs118020636	snp	A/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74645364	CATGGATATATAGTC[A/T]TGCATTGCTTGACAA	55159
rs118114423	snp	A/G	0.145305	0.227022	intron-variant	RFWD3	GRCh38.p7	16:74650792	TGAGGCGGGAGGATC[A/G]CTTGAGCCTGGGAGG	55159
rs118135741	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667483	ATCTGAGCTACTGAA[C/T]AGTCTCAAATCACTT	55159
rs118152452	snp	A/C	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74647100	CAAAAAAAAAAAAAG[A/C]TTCAATTTTATGTAC	55159
rs137924263	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663309	CTACTGTTAAAAGTA[A/C]AACAGAGTAAAAGAA	55159
rs137930597	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642788	ATGAGCCACTACACC[C/T]AGCCTATTTATTTTC	55159
rs137961728	snp	C/G	0.00122211	0.0246893	synonymous-codon	RFWD3	GRCh38.p7	16:74628465	ACCAGGCCTGTAGGT[C/G]ACAAGACAGTGCCGG	55159
rs137973735	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74653690	CAACTAAGTATTACT[A/G]ACAGGTGACCTACTA	55159
rs138005461	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74634476	AATAGCCTCGATCTC[C/T]TAGGCTCAAGCGATC	55159
rs138038179	snp	C/T	0.0158469	0.0875917	intron-variant	RFWD3	GRCh38.p7	16:74648851	AATGGTTTGGGAGGC[C/T]GAGGCAGGACGATAC	55159
rs138118160	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74658658	TGCACACTTCCTGAC[C/T]GTTTAGGTTATTCCC	55159
rs138183271	in-del	-/GTTTTTTTTTTTTTTTT/T	0.0130921	0.0798413	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668610	TTGTTGTTGTGGCAG[-/GTTTTTTTTTTTTTTTT/T]TTTTTTTGTGTGTGT	55159
rs138209252	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621538	AGACATTTTGAGTTC[A/G]TTTAACTCCAAATCC	55159
rs138316003	snp	G/T	0.00914312	0.0669923	intron-variant	RFWD3	GRCh38.p7	16:74629478	AGCCTGGCCAATATG[G/T]TGAAACCCCATCTCT	55159
rs138352411	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662657	AGAAGGAAATCAGTG[C/T]ATAGGTCCCTGATGA	55159
rs138389417	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74637504	TGGTGGTGGGCTCCT[A/G]TAATCCCAGCACCTC	55159
rs138396009	snp	C/T	0.000543832	0.0164809	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630840	TCGCACGTCATATAC[C/T]AGAATTGAACCATTG	55159
rs138435639	snp	G/T	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74634033	AGTCATGGTTTCAGG[G/T]GTGTATTACATATGT	55159
rs138454127	snp	C/T	0.00148263	0.0271867	missense	RFWD3	GRCh38.p7	16:74644639	GCCGGTGGTCCCCAG[C/T]ATTGGTCCACTGTTC	55159
rs138528783	snp	C/T	0.0119091	0.0762411	intron-variant	RFWD3	GRCh38.p7	16:74624902	GAGGCTGAAGGAGGA[C/T]TGCTTAAGCTGAGGA	55159
rs138539305	in-del	-/T	0.0271762	0.113356	intron-variant	RFWD3	GRCh38.p7	16:74639982	CTATTTTATTATTTA[-/T]TTATTGTTAATCTCT	55159
rs138626588	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667864	GGCAGAATGGAAGTA[A/G]TGATTCTGACAGATA	55159
rs138677232	in-del	-/ATTA	0.450985	0.148678	intron-variant	RFWD3	GRCh38.p7	16:74641470	GCCTGGCCTAAACAG[-/ATTA]ATTTTGACTAGAGAA	55159
rs138788771	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74654241	AAGTCTGTCAATTTT[C/G]TTGATCTTTTAGAAG	55159
rs138862404	snp	C/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74630366	TCTTCCCAAAGTGCT[C/G]GGATTACAGGCGTAA	55159
rs138875235	in-del	-/TACTA	0.0119091	0.0762411	intron-variant	RFWD3	GRCh38.p7	16:74639942	CACACTCACATAACT[-/TACTA]TAGTATACTGGTATA	55159
rs138910094	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74650022	TTTAGAGTCAATCCA[C/T]ATTTGCATCTGCAGC	55159
rs138963177	snp	C/G	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74626501	GATTTCCAGTGTCAT[C/G]CAGTCGGTAGGACAT	55159
rs138984449	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624387	CCCTGTCTTTGCCCT[C/G]ATGGAACTCACCCTT	55159
rs139051278	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662345	CTTTTATTTTCATCT[A/G]ACTTATGAGGAAATG	55159
rs139061578	snp	C/T	0.00795532	0.062565	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621843	GGGACTACAGGCATG[C/T]GCACCACTGCACCCA	55159
rs139079671	snp	A/T	0.0178098	0.0926698	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622101	TCAAAGAAAGTCAAA[A/T]CCTAAGCCTGCCCAG	55159
rs139223515	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664102	CTGCAAACTGAACAA[C/T]GTGAGATACTTCAAG	55159
rs139335083	snp	C/T	0.0170251	0.090679	intron-variant	RFWD3	GRCh38.p7	16:74658702	ATTATGGCTGCCAAA[C/T]AGCTTGACTGACATC	55159
rs139388237	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626754	GGCTAGCATCAGTGA[A/C]ATTTAGAACCATAGG	55159
rs139399858	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650937	CAACTATCTGATTGT[C/G]CAAAATACAGTTTAT	55159
rs139499768	snp	C/T	0.00874735	0.0655527	intron-variant	RFWD3	GRCh38.p7	16:74656457	TCTGGACAAAGTAAA[C/T]TGAAAACCTTGAAAT	55159
rs139528678	snp	C/T	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74638448	AAAAGCATAAATAGG[C/T]ATAACGAGGAACAAT	55159
rs139672835	snp	C/T	4.95405e-05	0.00497673	synonymous-codon	RFWD3	GRCh38.p7	16:74623931	TCGAGACCACAGTCA[C/T]TCCCACTTATAGATG	55159
rs139673643	snp	A/G	0.0267878	0.112589	intron-variant	RFWD3	GRCh38.p7	16:74635253	GCGCCACTGCAGTCC[A/G]GCCTAGGCGAAAGAG	55159
rs139816748	snp	A/C	0.00636936	0.0560724	intron-variant	RFWD3	GRCh38.p7	16:74637750	CATGTTCATTTCCTA[A/C]ACAACTTGGCAAATC	55159
rs139858023	snp	C/T	0.000307953	0.0124049	missense	RFWD3	GRCh38.p7	16:74649151	TTGGGGAGGGTCTTG[C/T]CTCCATCGATACATG	55159
rs139892316	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74626042	AATACAAAAATCAGT[C/T]GGGCATGGTGGTGGG	55159
rs139919392	in-del	-/CTCT	0.201418	0.245234	intron-variant	RFWD3	GRCh38.p7	16:74655620	TTTATTCTGTCTGTG[-/CTCT]CTCTCTTTTTTTTTG	55159
rs139957475	snp	A/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74660427	CACGGGAATCCAGCC[A/T]GGACGACAGAGTGAG	55159
rs140028690	snp	C/T	1.6473e-05	0.00286988	missense	RFWD3	GRCh38.p7	16:74644363	CTCTTACCACCTACC[C/T]TTTCATGCGCTCCTG	55159
rs140241823	snp	A/C	0.0023933	0.0345097	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622024	TTAAGATTCACATAA[A/C]GTCCCTCATAGTTAA	55159
rs140344281	snp	A/T	0.00199481	0.0315187	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621229	TTGCAGTGAGCCAAG[A/T]TGGCGCCACTGCACT	55159
rs140448448	snp	C/T	0.0154538	0.0865337	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623140	CCAATCCTGAGATCC[C/T]AAGCTGGCTAGAAAA	55159
rs140480568	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657930	GTTAGGGTGTTGACA[C/T]GTATATCAATAGAAT	55159
rs140507794	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668334	CTGAAGTGGGAGAAA[A/G]AAAACACAGGAAAGA	55159
rs140551878	snp	C/T	0.0182019	0.0936463	intron-variant	RFWD3	GRCh38.p7	16:74642283	ACGCACCACCACATC[C/T]GGATAATTTTTTGTA	55159
rs140637217	snp	A/G	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74633487	AAAAAATTATGCAGC[A/G]AGAAAGAAGTCAGAC	55159
rs140714019	snp	C/G	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74647554	TGACTTCCCACAGTG[C/G]TGGGATTACAGGTGT	55159
rs140802226	in-del	-/A	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74647757	CCAACATACCCAGCT[-/A]ATCTTTGCATTTTTA	55159
rs140812890	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622626	TCAGAAGTGTTTTAT[A/G]ATAAAAACGATAACA	55159
rs140821881	snp	C/G	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74661198	GTCTTCTCCCAAGAC[C/G]TCCACTTCTGTCAGG	55159
rs140932990	snp	C/T	0.00557542	0.0525036	intron-variant	RFWD3	GRCh38.p7	16:74651425	GAGTTTATGACCAGC[C/T]GGGGCAACATGGAAA	55159
rs141004151	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74653816	TTTGGCTGCAATTTA[C/T]TGATGAATTAGGGCT	55159
rs141012566	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635933	CTCCCTAAATTCTCT[C/T]ATTTGGAAATTGTTA	55159
rs141113066	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666428	CTCAGAGCGGGCGCA[A/G]GCAACGCCGCTGAGG	55159
rs141146534	snp	A/T	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74644581	TTAAGCCACGTGGAA[A/T]TGCACCTATACCCAA	55159
rs141148944	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657646	ACACCCGACTAATTT[G/T]TGTATTTTTAGTAGA	55159
rs141177297	snp	A/G	0.00755907	0.0610114	intron-variant	RFWD3	GRCh38.p7	16:74659510	TGAGGCACAAGAATC[A/G]CTTGAACCCGGGAGC	55159
rs141199869	snp	A/G	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74646615	ACATGGTGAAACCTC[A/G]TCTCTACTAAAATAC	55159
rs141258223	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74643516	CTAGATCAAAGGCTT[C/T]AGAGACACATTTCCA	55159
rs141265206	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642684	TTTTATTAGAAACAA[C/G]GTCTCACAATGTTGC	55159
rs141321984	snp	C/T	0.000214219	0.0103472	missense	RFWD3	GRCh38.p7	16:74626506	CCAGTGTCATCCAGT[C/T]GGTAGGACATTTCCA	55159
rs141347512	snp	C/T	0.0158469	0.0875917	intron-variant	RFWD3	GRCh38.p7	16:74637004	AGGCGTGAGCCACCG[C/T]GCCCGGCCAGAACTG	55159
rs141439715	snp	C/G/T	1.76446e-05	0.00297018	missense	RFWD3	GRCh38.p7	16:74637933	GTGCTGATTCTAACT[C/G/T]GGCCTGTTTCCTTAG	55159
rs141461191	snp	C/G	0.0182019	0.0936463	intron-variant	RFWD3	GRCh38.p7	16:74639127	CACGGCTACCTCCGC[C/G]CCCCGGGTTCAAGAG	55159
rs141601833	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634216	TTTGTCAGTCAAGAT[A/T]TGTCACATCTGTCTG	55159
rs141662063	snp	C/T	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74625632	TAGAACGCCCACAAC[C/T]CGGACTTGTGTATAT	55159
rs141682107	snp	A/G	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74629397	GGCATGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	55159
rs141685768	snp	C/T	0.000115457	0.00759706	missense	RFWD3	GRCh38.p7	16:74628581	CCCAGAATGAAGCAT[C/T]CTCCAAGGTTCCAGC	55159
rs141695794	snp	A/G	0.0182019	0.0936463	intron-variant	RFWD3	GRCh38.p7	16:74637443	ACTAGCCTGGCCATC[A/G]TGGTGAAACCCTGTC	55159
rs141723558	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74665752	TTTCTTTCTTTCTTT[-/T]CTTTTTTTGAGATGG	55159
rs141811722	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662397	AAGCACCTGTTATGC[A/G]GACAAGACACCCTAG	55159
rs141948440	in-del	-/A	0.0182019	0.0936463	intron-variant	RFWD3	GRCh38.p7	16:74638347	ATACTCAAATAATAT[-/A]ACCCAAAAAAGAATC	55159
rs141980359	snp	A/G	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74630237	AGTAGCTGGGATTAC[A/G]GGCGTGTGCCACCAC	55159
rs142048133	snp	A/G	4.95896e-05	0.00497919	intron-variant	RFWD3	GRCh38.p7	16:74651909	AGTCCAAACCTGGGT[A/G]AAATACTGACCTTCT	55159
rs142194955	snp	A/G	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663884	CAAAAGGCAATATTG[A/G]AAGATGGCGCTAAAA	55159
rs142363887	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638368	AAAAAGAATCTGAAG[C/T]TAAAAAGAGCAAAAG	55159
rs142393106	snp	A/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664599	AAAAAATACAAAAAA[A/T]TTAGCCAGCCGTGAT	55159
rs142439147	in-del	-/GT			intron-variant	RFWD3	GRCh38.p7	16:74650389	GGGGGTGGGGGGCTG[-/GT]GTGTGTGTGTATACA	55159
rs142465778	snp	C/T	0.199564	0.24486	intron-variant	RFWD3	GRCh38.p7	16:74641706	AAGGCAGGCTGATCA[C/T]GAGGTCAGGAGTTCC	55159
rs142472584	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661660	TTATAACCAGTTTTC[C/T]GGTTTGCCCTTAGAA	55159
rs142592065	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74650890	CAAAAAAAACAAATG[-/A]AAAAAAAAAACAACA	55159
rs142695331	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639635	TTTAATGCAATTTCA[A/G]TCAAGATCCCAAAGG	55159
rs142704686	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668063	GGCGGACCTCTGCAG[G/T]CATTATTAACTAGGG	55159
rs142800777	in-del	-/GAG	1.64776e-05	0.00287028	cds-indel	RFWD3	GRCh38.p7	16:74636364	GAAGAAAAGAGGCCT[-/GAG]GAGAAGGCTGTGATA	55159
rs142849013	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637695	GTGTGTAGTAAGTTT[C/T]GAACAGATGCCCTAA	55159
rs142872841	snp	C/T	0.0314385	0.121371	intron-variant	RFWD3	GRCh38.p7	16:74643898	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG	55159
rs142915660	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74646356	ACTCCAGCATGAGGG[A/G]CAGAATGAGACCCTG	55159
rs143069050	snp	A/C/G	4.94176e-05	0.00497059	missense, synonymous-codon	RFWD3	GRCh38.p7	16:74644433	GACGACAATGTCACT[A/C/G]TGCCTGGCTTTCTTG	55159
rs143070620	snp	C/T	1.64912e-05	0.00287147	missense	RFWD3	GRCh38.p7	16:74649133	GATGTTCATATTACC[C/T]GTTTGGGGAGGGTCT	55159
rs143084121	snp	A/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639428	CCATCGTATATGCAA[A/T]CTGTCATTGACCCAA	55159
rs143158713	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626092	CTCAGGAGGCTGAGG[C/G]AGGAGAATCACTTGA	55159
rs143173893	snp	C/T	0.00125132	0.0249818	synonymous-codon	RFWD3	GRCh38.p7	16:74626484	CTGGCAGGAGCAGAT[C/T]GGATTTCCAGTGTCA	55159
rs143191542	snp	C/G	0.00795532	0.062565	intron-variant	RFWD3	GRCh38.p7	16:74643112	GAAAACTAAAATAAT[C/G]TGTACAGTGACTACC	55159
rs143202479	snp	A/G	0.00953873	0.0683987	intron-variant	RFWD3	GRCh38.p7	16:74655499	TGATTCGCCCGCCTC[A/G]GCCTCCCAAAGTCCT	55159
rs143262250	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74633212	AACCCAGGAGGCGGA[A/G]GTTGTAGTGAGACAA	55159
rs143335463	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621703	TTGTTTGTTTTTTTT[-/T]GAGATGGAGTCTTGC	55159
rs143437222	snp	C/G	0.0107246	0.0724382	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622897	ATAAAGAACACTTAA[C/G]AACAGCCCCTCAGTC	55159
rs143501341	snp	A/G	0.0197687	0.0974348	intron-variant	RFWD3	GRCh38.p7	16:74660577	CCAAGACTATGAAAG[A/G]AAATTAATTAATTGT	55159
rs143543169	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623231	GAACTTAATGCACTA[C/G]GCATTAGCAAAGGGA	55159
rs143577108	snp	A/G	3.29457e-05	0.00405854	synonymous-codon	RFWD3	GRCh38.p7	16:74661075	AAGTCTCTGCAGTCC[A/G]CTGATGAAGTTGGTC	55159
rs143641416	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654588	CAATGGCCTCTAAGT[A/G]TTCAAATTAAGGGAA	55159
rs143700326	snp	C/T	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74642866	GGGTAAAAGGCTGTT[C/T]GTTTTATTAGTCTGT	55159
rs143761067	snp	A/G	0.00636936	0.0560724	intron-variant	RFWD3	GRCh38.p7	16:74640002	TGTTAATCTCTTACT[A/G]TTCCTAATTTATAAA	55159
rs143834179	snp	C/T	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74658694	GGAGACAGATTATGG[C/T]TGCCAAATAGCTTGA	55159
rs143980305	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660016	GCTGTGATTGCACCA[C/T]TGCACTCCAGCCTGG	55159
rs144055376	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654808	TTATTGCTGATATGG[A/G]GACAGTTTTAGTGGT	55159
rs144075094	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638244	CTAGTGTTCAGCTAC[C/G]GCAAATTGTAAAAGA	55159
rs144193063	snp	C/G	0.00557542	0.0525036	intron-variant	RFWD3	GRCh38.p7	16:74641028	TTAGAAAAGTAATTT[C/G]ACAATATTTAGGTAA	55159
rs144322244	snp	A/G	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74625331	TTTGAGACCAGCCTG[A/G]GAAACATGGCAAAAC	55159
rs144389371	snp	C/T	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74632456	AGGTCATCATAACAC[C/T]GATACGAATTCCATG	55159
rs144397177	snp	A/G	0.00118759	0.0243389	synonymous-codon, intron-variant	RFWD3	GRCh38.p7	16:74630927	AGGACGTCCAGCATT[A/G]TAAGTCTGGACCACG	55159
rs144438494	snp	A/G	3.29935e-05	0.00406149	synonymous-codon	RFWD3	GRCh38.p7	16:74623940	CAGTCACTCCCACTT[A/G]TAGATGTGGACCATC	55159
rs144458965	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638453	CATAAATAGGCATAA[C/T]GAGGAACAATGTATC	55159
rs144459760	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668660	AAACCAACCATGTAA[A/G]TCCCTTCTCTAATAT	55159
rs144461382	snp	A/C	0.0182019	0.0936463	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667936	GAAGAGAGAACCGCT[A/C]AACAGGGGAGTAAAG	55159
rs144727254	snp	A/G/T	3.29648e-05	0.00405974	missense	RFWD3	GRCh38.p7	16:74652034	ACTCTTCAGATACAG[A/G/T]ATTCCTAGTCTCTGA	55159
rs144729411	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74665361	GGAAGCCGAGGGCAG[A/T]CCACTTGAGGTCGGA	55159
rs144731516	in-del	-/AAGAA	0.188631	0.242351	intron-variant	RFWD3	GRCh38.p7	16:74628992	TGGGTTTAGCCACAT[-/AAGAA]AAGTCAGAAAAGAAA	55159
rs144755231	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74657775	CACTGCGCCTAGCCA[C/G]GTTTTCTTTTTAGAC	55159
rs144820486	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654161	CTATTTGGTAGTCAT[C/G]TCCTCTCTTTCATTC	55159
rs144876115	snp	C/G	0.00358779	0.0422022	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622554	CTCTGGGGAAATCTA[C/G]TGCAACAACCCCTTG	55159
rs144983290	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74627304	TTTAGGGCTAGCATA[A/C]ATTATTTGAAACCCA	55159
rs145019432	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664549	ACCAGGAGTTGGAGA[C/T]CAGCCTGGGCAACAC	55159
rs145084957	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651559	AAGAAGCGGAAGTTG[C/T]AGTAAGCTGAGATTG	55159
rs145129425	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74637096	AGGGTTGAAAGTCCT[C/T]AATGGTGGTTTCGTT	55159
rs145150318	snp	C/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74646847	GGAGCCCGAAGCGGG[C/T]GGATCACCAGGTCAG	55159
rs145310076	snp	C/T	3.29457e-05	0.00405854	synonymous-codon	RFWD3	GRCh38.p7	16:74661108	TGAATGCAACGAAGA[C/T]GCTGGGATGGTGTGA	55159
rs145324335	snp	C/T	8.2573e-05	0.00642493	missense	RFWD3	GRCh38.p7	16:74660960	TCCTCTGAGACCCTC[C/T]GGCTCTTGCCCTCCG	55159
rs145385731	snp	C/T	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74637876	CACGCCTTTGAAGCC[C/T]AGTGCACTTATCAGT	55159
rs145419495	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74648839	GACTACAATCTCAAT[A/G]GTTTGGGAGGCCGAG	55159
rs145511565	snp	A/G	1.65312e-05	0.00287495	synonymous-codon	RFWD3	GRCh38.p7	16:74661318	TACCCCCTGGCTGCT[A/G]ACCACATCAGCAGGA	55159
rs145544287	snp	G/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74660817	TATGAGGAACTGGGG[G/T]TCAGAAGTTACCTGA	55159
rs145544625	snp	A/T	0.00557542	0.0525036	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622033	ACATAACGTCCCTCA[A/T]AGTTAAGTCTCTTGC	55159
rs145568558	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74652789	TAACTCCTGGAATAA[C/T]AAGGCATACTCCAGT	55159
rs145714627	snp	A/G	5.00246e-05	0.00500098	synonymous-codon	RFWD3	GRCh38.p7	16:74624027	CAACACAGGCTGATC[A/G]GTCTGTAGGTCCTGG	55159
rs145725234	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74636149	AGTATTTCTACCCTC[C/T]TGGTTAATAAATTTA	55159
rs145776653	snp	A/T	0.000399281	0.0141238			GRCh38.p7	16:74633604	TGGGGATGGGAGAGG[A/T]GGGAGGGGCAGGTGA	55159
rs145904981	snp	C/T	0.0341408	0.126114	intron-variant	RFWD3	GRCh38.p7	16:74636779	AGTGCAGTGGGACCA[C/T]GTTGGCTCACTGCAA	55159
rs145970939	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667823	GTCTCCTTCAGCAAC[A/G]ATTTCTTCTTCAGCA	55159
rs145971185	snp	A/G	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74625714	TCAATGAAAGTTAGC[A/G]CTAGCTTCTAGAGTG	55159
rs145972504	in-del	-/A	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74661636	GACTTTCCTCTCTAT[-/A]ACAAGCATTTATAAC	55159
rs146049115	snp	A/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74644183	TGCAGACTTCCTTAA[A/G]AAGATGATCAGACAT	55159
rs146092738	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649566	GTCATTATACTTGCA[A/G]AAACTTCTGCAACAC	55159
rs146124091	snp	C/G	1.65921e-05	0.00288024	missense, intron-variant	RFWD3	GRCh38.p7	16:74630949	TGGACCACGGTATTT[C/G]TCTCCAGGCTGTGGA	55159
rs146196899	snp	A/G	4.94311e-05	0.00497123	missense	RFWD3	GRCh38.p7	16:74644612	AGAGATGCCCACAGC[A/G]TAATGCTGAGAGCCG	55159
rs146216466	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74634431	ACTCTGTCACCCATG[C/T]TAAGGTGCAGTGGCA	55159
rs146290188	in-del	-/G	0.202651	0.245475	intron-variant	RFWD3	GRCh38.p7	16:74660029	CACTCCAGCCTGGGG[-/G]AGCACAGTGAGACCC	55159
rs146313026	snp	A/T	0.00597247	0.0543191	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662007	ATCCCTTTCATTATT[A/T]TTGTTTTCCATCTCT	55159
rs146389721	snp	G/T	3.29468e-05	0.00405861	missense, intron-variant	RFWD3	GRCh38.p7	16:74630877	CCAGCATAGATGTAG[G/T]TAGCCTCATCAAGAC	55159
rs146431141	snp	C/G	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74660085	AAAAACAAGAAGAAA[C/G]AGAAAACAAAGGGAT	55159
rs146451559	snp	C/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74658698	ACAGATTATGGCTGC[C/G]AAATAGCTTGACTGA	55159
rs146514050	snp	C/T	0.00755907	0.0610114	intron-variant	RFWD3	GRCh38.p7	16:74657636	ACCCGCCACCACACC[C/T]GACTAATTTTTGTAT	55159
rs146554355	snp	C/G	0.0142736	0.0832652	intron-variant	RFWD3	GRCh38.p7	16:74641212	TTGTTGCCCAAGCAG[C/G]AGTGCAATGGTGCGA	55159
rs146574678	snp	C/T	0.00148265	0.0271869	missense	RFWD3	GRCh38.p7	16:74623954	TATAGATGTGGACCA[C/T]CTTCTCTGTTAAGGT	55159
rs146632750	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638502	CAAGAATAACAAATA[C/T]ATATTTGTATGTACC	55159
rs146675982	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74626707	ACAAATGAAAGAACA[A/G]TATCACAGCATCAAT	55159
rs146756215	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623077	GACCTATCACTCATC[C/T]TTTCCTGGCAAGAGA	55159
rs146925442	snp	C/G	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74642740	TCAAGCAATCCTCCT[C/G]CCTCGGCCTTCCAAA	55159
rs146942008	snp	A/G	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74639662	AAGGTGTTTTTCATG[A/G]AACTTAACAAATTAA	55159
rs146972288	snp	C/T	1.79965e-05	0.00299965	synonymous-codon	RFWD3	GRCh38.p7	16:74637940	TTCTAACTCGGCCTG[C/T]TTCCTTAGCATCTGT	55159
rs146989549	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74654028	GTGTTGTTTTTTTTT[-/T]AGCATAACCACAAGG	55159
rs146995643	snp	A/G	1.65293e-05	0.00287479	synonymous-codon	RFWD3	GRCh38.p7	16:74626529	CATTTCCATCAGCAC[A/G]CTTCGTATGGTGGTG	55159
rs147029804	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74629401	TGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTC	55159
rs147046806	snp	C/T	0.0178098	0.0926698	intron-variant	RFWD3	GRCh38.p7	16:74624692	GTGAGCCACCGCGTC[C/T]GGCCTCTAAAAATTT	55159
rs147395572	snp	A/C	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74635200	CAGAATGGCATGAAC[A/C]CGAGAGGTGGAGCTT	55159
rs147431582	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637732	ATAAAATAAGGAGTT[A/G]GTCATGTTCATTTCC	55159
rs147517120	snp	C/T	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74655506	CCCGCCTCGGCCTCC[C/T]AAAGTCCTGGGATTA	55159
rs147552508	snp	C/G	0.0236746	0.106192	intron-variant	RFWD3	GRCh38.p7	16:74646994	CGGGAGGCTGAGGCA[C/G]GAGAATGGTGTGAAC	55159
rs147588332	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651856	AAATCTAGTTTCTAG[C/T]CTTCCGAAATTTAAG	55159
rs147622872	in-del	-/AG			utr-variant-5-prime	RFWD3	GRCh38.p7	16:74666850	AGTTACCTCGGCCGC[-/AG]ACTCCGAATGCACCT	55159
rs147656588	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632744	CAAACTAGTTTTTCA[A/G]GTAGCTCCTTCGTCC	55159
rs147669381	snp	C/T	4.94189e-05	0.00497062	missense	RFWD3	GRCh38.p7	16:74661005	TCCTTCTTGTTCTCA[C/T]TGGCCCTACACTGTG	55159
rs147727063	snp	A/G	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74646454	TGAGACAACACAGGC[A/G]TGTGCCACCATACAC	55159
rs147795772	snp	C/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74642402	GTGCTAGGATTTCAG[C/G]TGTGAGCCACTGTGC	55159
rs147831409	snp	A/C	8.29043e-05	0.0064378	intron-variant	RFWD3	GRCh38.p7	16:74632474	TACGAATTCCATGCT[A/C]CTCAACACCAAAGAG	55159
rs147848964	snp	G/T	8.44944e-05	0.00649924	synonymous-codon	RFWD3	GRCh38.p7	16:74637895	GCACTTATCAGTGAG[G/T]ACCTGCAGTTGGAGT	55159
rs147863510	snp	A/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74665628	GCCGGGCGTGGTGGC[A/G]CGCACCTGTGGTCCC	55159
rs147900771	snp	G/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74629056	TCCCAAGTTGTAGTT[G/T]ACAGACCCCACAATT	55159
rs148002837	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637364	CAGGTGCAGTGCTCA[C/T]GCCTGTAATCCCAGC	55159
rs148058403	in-del	-/ATAG	0.0267878	0.112589	intron-variant	RFWD3	GRCh38.p7	16:74666160	TGGGGAAAGAAAGAC[-/ATAG]ATAGATTAGATAGAC	55159
rs148091067	snp	C/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74654796	GATAAGACAGCCTTA[C/T]TGCTGATATGGAGAC	55159
rs148112381	in-del	-/AC			intron-variant	RFWD3	GRCh38.p7	16:74653035	AGGAAGGATCTAGGG[-/AC]ACACACACACAGACA	55159
rs148162382	snp	G/T	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74666238	TTGATTAGATACATA[G/T]ATATTAAATCCCTGT	55159
rs148181010	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639431	TCGTATATGCAATCT[A/G]TCATTGACCCAAAGG	55159
rs148229842	snp	C/T	0.000230616	0.0107357	synonymous-codon	RFWD3	GRCh38.p7	16:74644574	TTGTCCTTTAAGCCA[C/T]GTGGAAATGCACCTA	55159
rs148234796	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643330	CTAATAACATGCTTC[C/T]ACAGGACAACATATG	55159
rs148374451	snp	C/T	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74633459	AAAGGAATTAACTAC[C/T]AATATATACAATAAA	55159
rs148407492	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74631983	ACATATTTTGTAATA[C/T]ACATAGTTTCAAAGA	55159
rs148545931	snp	G/T	0.000775891	0.019681	missense	RFWD3	GRCh38.p7	16:74652081	GGCAAGTCAGGCTGG[G/T]TCCTGCTCACCTGAA	55159
rs148561736	snp	G/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74659040	TCTGAGATTACAGGC[G/T]TGAGCCACTATGCCC	55159
rs148596004	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74645212	GTTGTGGGTAAATGA[C/G]ATATGGACATGCTTA	55159
rs148684134	snp	C/T	0.160938	0.233598	intron-variant	RFWD3	GRCh38.p7	16:74635055	GGAGGCCGAGGCGGG[C/T]GGATCATGAGGTCAG	55159
rs148732937	snp	A/G	0.000115307	0.00759211	synonymous-codon	RFWD3	GRCh38.p7	16:74636422	GTATGCCATGATCCG[A/G]CAGTTTCCTGCCTGA	55159
rs148738112	snp	C/G	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74638280	CTGACATGTTAAAAG[C/G]CCAAGGTTACTGGAT	55159
rs148738474	in-del	-/AGAG			intron-variant	RFWD3	GRCh38.p7	16:74626819	AAGAGAAAAACAATT[-/AGAG]CTGTGAGTTGTCTGT	55159
rs148829079	in-del	-/TTT			cds-indel, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621696	CAGGGTTTTTTTTTG[-/TTT]GTTTGTTTTTTTTGA	55159
rs148851729	snp	A/T	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74661421	TTTAACTGCACCTGA[A/T]CATCATATTCCATTG	55159
rs148877733	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74660876	GAATGGCAGAGCCTC[A/G]GTTTCATAATTTCTA	55159
rs148909927	snp	C/T	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74647945	TATTCTGCCTGATTT[C/T]TTTTTAATTTTAATT	55159
rs149000471	snp	G/T	0.000296623	0.0121747	missense	RFWD3	GRCh38.p7	16:74636538	AGCCCCTGGGTTGCT[G/T]TAAATTCTGACTTTG	55159
rs149050123	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74639372	TTACAACATCACTTA[C/T]GCAACAGAATTTTCA	55159
rs149052600	snp	C/T	6.58903e-05	0.00573941	missense	RFWD3	GRCh38.p7	16:74644371	ACCTACCTTTTCATG[C/T]GCTCCTGTTCACTAG	55159
rs149070662	snp	A/G	0.00639846	0.0561986	intron-variant	RFWD3	GRCh38.p7	16:74651906	GTGAGTCCAAACCTG[A/G]GTAAAATACTGACCT	55159
rs149086252	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74628144	AGTGATCTCAAGGTG[A/G]CTCAATGACCTAGAG	55159
rs149104426	snp	A/C	3.29457e-05	0.00405854	missense	RFWD3	GRCh38.p7	16:74626366	AATTTGCTGCTTCAT[A/C]CCCAGTACACACCAG	55159
rs149139641	snp	C/G	0.0115144	0.0749975	intron-variant	RFWD3	GRCh38.p7	16:74633210	TGAACCCAGGAGGCG[C/G]AGGTTGTAGTGAGAC	55159
rs149243114	snp	C/G/T	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667932	TTGAGAAGAGAGAAC[C/G/T]GCTAAACAGGGGAGT	55159
rs149366908	snp	A/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74640677	AGGCGCAGTGGCTCA[A/T]GCCTGTAATCCCAGC	55159
rs149384933	snp	C/G	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74654260	ATCTTTTAGAAGAAC[C/G]AACTTTTTGATTCGT	55159
rs149403255	snp	A/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74630474	CCAAGAAAATACAAC[A/T]AAGGTCACACAACTT	55159
rs149647106	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74625248	AAAAGGTAGAGAGCA[C/T]GGTGGCTCATGCTTG	55159
rs149696131	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656681	CAGGTTGGTCTTGAA[C/T]TCCTGAGCTCAGGCA	55159
rs149759685	snp	C/T	0.000662175	0.0181838	synonymous-codon	RFWD3	GRCh38.p7	16:74624015	TGGGCAGATGTCCAA[C/T]ACAGGCTGATCGGTC	55159
rs149767844	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636062	GTAAGTTGAGGACAT[A/G]TAAGTCCTTCTTGGA	55159
rs149834080	snp	C/T	3.29511e-05	0.00405887	synonymous-codon	RFWD3	GRCh38.p7	16:74649198	TGAGACACCTGCTAG[C/T]TGCTCTGCCAAGTCA	55159
rs149839134	snp	A/G			missense	RFWD3	GRCh38.p7	16:74644735	ACTTCTGGGGAGATG[A/G]CTAGATGGAAAGCAG	55159
rs149910004	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622139	GACAAAGCCAGCCAG[G/T]ACCTGACCACCTGTA	55159
rs149927398	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664120	GAGATACTTCAAGTT[C/T]TAAACATTTTTTGTA	55159
rs149963383	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74627187	CATGAGTAGACCCAC[C/T]CACAACTAGCAGAAG	55159
rs150067481	snp	C/T	0.00953873	0.0683987	intron-variant	RFWD3	GRCh38.p7	16:74651221	AGGGGTCTCTGCCTA[C/T]GACTATTAAATAAAG	55159
rs150095922	in-del	-/G	0.4582	0.138394	utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621694	CAGGGTTTTTTTTTG[-/G]TTTGTTTGTTTTTTT	55159
rs150100948	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647580	GGTGTGAGCCACTGC[A/G]CCCGGCCAACATTAT	55159
rs150151715	snp	C/G	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74661311	TGGATGGTACCCCCT[C/G]GCTGCTGACCACATC	55159
rs150177046	in-del	-/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667144	GTTTTTTTTTTGTTT[-/G]GTTTTTTTTTTTTTT	55159
rs150221303	snp	A/G	0.000412143	0.0143493	missense	RFWD3	GRCh38.p7	16:74623987	CCAAGTAGCTGTTAC[A/G]GTTCACCTCAAATGG	55159
rs150237842	snp	A/G	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74666754	CGAAGCTAGAGGCCC[A/G]AGGCCTGAGGAGAAG	55159
rs150273155	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630268	GCATGGCTAACATTT[C/T]TTTGTATTTTCAGTA	55159
rs150363088	snp	A/G	0.00755907	0.0610114	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621370	CTGCCTCTAGAAGTG[A/G]AAGAGACAAAAGGCA	55159
rs150468265	snp	A/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74642297	CCGGATAATTTTTTG[A/T]ATTTTTAGTAAAGAT	55159
rs150483097	snp	A/C	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662463	TAGATTCTAGCAAGT[A/C]AGATGTCAATAAACA	55159
rs150675219	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622034	CATAACGTCCCTCAT[A/G]GTTAAGTCTCTTGCT	55159
rs150744170	snp	C/T	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74659818	CACAAATTATCCCAT[C/T]AGCTTCCTCATTTGT	55159
rs150780191	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643543	TCCAAGGATGTCTCA[A/T]AATGATTTTGCCTGT	55159
rs150797885	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663984	AAAACACAGAACAAA[A/G]CCCTTCTCCCCCTAT	55159
rs150834068	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650070	ATTATCTCTGTAGAC[C/T]TGCCTTTTCTGGACA	55159
rs150855269	in-del	-/A	0.0134861	0.0810011	intron-variant	RFWD3	GRCh38.p7	16:74642004	TATCATACTATGTAT[-/A]ATTTACAAATACATA	55159
rs150991472	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623545	ACAGGACAACTCAGA[C/T]GGGATGTCATATTCC	55159
rs151008735	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74632099	GACCAAAAAAAACAG[A/G]GCTAAGGTCGGCTGG	55159
rs151061145	snp	C/T	0.000561362	0.0167441	missense	RFWD3	GRCh38.p7	16:74661305	GGAGGATGGATGGTA[C/T]CCCCTGGCTGCTGAC	55159
rs151148478	snp	C/T	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74652242	GCCATTAAATGCTGC[C/T]TTTGAAAGCTGAAGC	55159
rs151239809	snp	C/T	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74638401	GACATCAAGCAAATA[C/T]TAACAAAGGAAAGAC	55159
rs180676535	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622883	GATAACTGGAATGTA[C/T]AAAGAACACTTAAGA	55159
rs180683448	snp	C/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74639407	CATTATAATCTTATG[C/G]GGCCACCATCGTATA	55159
rs180685310	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74653862	CTAGAACAAAATAAA[C/T]ACTACTCAGTGTCCA	55159
rs180689746	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632988	TCATTTAAAAAAGTA[C/T]AACCCAGGCCAGGCA	55159
rs180927860	snp	C/T	0.00835141	0.0640778	intron-variant	RFWD3	GRCh38.p7	16:74636944	TCTTGAACTCCTGAC[C/T]TCAGGTGATCCACCC	55159
rs180929467	snp	C/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74649335	GTGTTCCTGCAAAAA[C/G]GATGACAACTTCCCC	55159
rs180938488	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74666686	CGTGCAGCCCACCTC[A/G]TGGGGTGTCTCCTGA	55159
rs180953067	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74627746	TTAGGCCATCTGCCA[A/G]GACAGAGGAGTATCC	55159
rs180964415	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74656969	AATTGATCTCATTCC[C/T]AGATTTTCCTTTCCT	55159
rs180989334	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74643575	TACATCCAAACCAGT[A/G]AAGTGTGAACCCATG	55159
rs181137589	snp	A/C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660372	GCAGGAGAATCGCTT[A/C/G]AATCTGGGAGATGGA	55159
rs181170672	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632233	GTCTCTACTACAAAA[A/C]TAGAAAATATTAGCC	55159
rs181176161	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646462	CACAGGCGTGTGCCA[C/G]CATACACCAACCATG	55159
rs181226018	snp	C/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74639908	AAATATCGAGATATG[C/T]TGAGAGAGAGATGGA	55159
rs181226970	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623737	CATCAATTACTCTTT[C/T]AGTGGACATAACAGA	55159
rs181346886	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657607	CAGTCTCCTGAGCAG[C/G]TGGGATTATGGGCAC	55159
rs181382082	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643879	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	55159
rs181786689	snp	A/C	1.6477e-05	0.00287024	missense	RFWD3	GRCh38.p7	16:74660987	TCCGTGAAGCAGATA[A/C]CCTCCTTCTTGTTCT	55159
rs181816400	snp	A/G	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74632406	CAAAAAAACAAAACA[A/G]AACAAAACAACAACA	55159
rs181873122	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74636034	TCAAACATTTCCAGT[C/G]TAAAATGCATCTGTA	55159
rs181878006	snp	G/T	1.64844e-05	0.00287087	synonymous-codon	RFWD3	GRCh38.p7	16:74649141	TATTACCTGTTTGGG[G/T]AGGGTCTTGCCTCCA	55159
rs181999564	snp	C/T	6.58924e-05	0.0057395	intron-variant	RFWD3	GRCh38.p7	16:74644467	CACTAAAGAACCCAA[C/T]AGGACATAATTAGAG	55159
rs182025444	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74646614	GACATGGTGAAACCT[C/T]GTCTCTACTAAAATA	55159
rs182041998	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74665583	ACTCTATCTCAAAAA[A/C]AGAAAGAAAAAAGAA	55159
rs182208394	snp	G/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74651149	AGTGGTAAAATATAC[G/T]GAAAGAGCGCCCTCT	55159
rs182213261	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668477	AACTCAGTGATTTGA[A/G]GATGGAGGAGTCGTT	55159
rs182295291	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74658972	TGGGGTTTCACCATG[G/T]TGGCCTCGAACTCCT	55159
rs182322880	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647038	CCTGCAGTGAGCCGA[G/T]ATCATGCCACTGCAC	55159
rs182325536	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74629286	TGTTTTATTTTCCCT[A/G]TCACAATAAAGGTAA	55159
rs182358109	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74629386	GTGTTTGGCTGGGCA[C/T]GGTGGCTCACGCCTG	55159
rs182584463	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74633565	AATGCAAACTCATCT[A/G]TAGTGACAAAAAGCA	55159
rs182594292	snp	C/T	0.00050081	0.0158163	missense	RFWD3	GRCh38.p7	16:74661397	GGAGCTGGCTGTTGT[C/T]CGGCATGATTTAACT	55159
rs182598378	snp	C/T	0.00953873	0.0683987	intron-variant	RFWD3	GRCh38.p7	16:74647609	ATTATTACTATTCTT[C/T]GAGATGAAGTCGTGC	55159
rs182603237	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662150	AACTAAAAAAAAAAA[C/T]TTTTTTTTGTTATAT	55159
rs182611277	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659304	GAAACACCACTCACA[A/G]CTCTCAACCATGGAA	55159
rs182621053	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74638329	CTGTTGGTTGTTCAT[A/G]AGATACTCAAATAAT	55159
rs182813060	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74629830	ACTTCAGATTTTGGC[C/G]AGGTCACAGACCCTA	55159
rs182813795	snp	A/G	0.00557542	0.0525036	intron-variant	RFWD3	GRCh38.p7	16:74645184	AAATTGATGTCTGAT[A/G]ACACCAAGCACTGTT	55159
rs182822728	snp	A/T	0.00755907	0.0610114	intron-variant	RFWD3	GRCh38.p7	16:74659703	CTGGAGCCACAGTCA[A/T]GGCAAGCCCCAACAT	55159
rs182847929	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642315	TTTTAGTAAAGATGG[C/G]GTTTTGCCATGCTGC	55159
rs182879460	snp	C/G	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74644799	TCTTGAAGAAGATGT[C/G]CAACTAAGAAATTAA	55159
rs182906943	snp	C/T	0.0146672	0.084371	intron-variant	RFWD3	GRCh38.p7	16:74654939	GGAAGCTGCAGGAAG[C/T]TGGAAGAAAGCAGAG	55159
rs182933568	snp	A/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74624388	CCTGTCTTTGCCCTC[A/T]TGGAACTCACCCTTT	55159
rs182940452	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74640561	AGCTACTCAGGATGC[C/T]GAGGTTGGAGGACTG	55159
rs183141835	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667734	GTGAATTGTGGTCCT[A/G]TTGTGGGAACAACCA	55159
rs183158248	snp	C/T	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74655921	ACTGTTGAAACCTAC[C/T]ATTCAGAAAAAAGGA	55159
rs183164422	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637762	CTAAACAACTTGGCA[A/T]ATCCTATTTGTTTCT	55159
rs183171624	snp	A/T	0.00557542	0.0525036	intron-variant	RFWD3	GRCh38.p7	16:74650891	CAAAAAAAACAAATG[A/T]AAAAAAAAACAACAA	55159
rs183192286	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74625229	GTAGAGAGGGACAGA[A/G]AAAAAAAGGTAGAGA	55159
rs183224118	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650117	TCATAAACTATGTTG[G/T]TTTACTGTTACATAA	55159
rs183422799	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667541	CAAAAGAAAGGGGCC[C/T]CCGGAATTCTCCAGC	55159
rs183422964	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655238	GGTGACTTCAGTTGA[A/G]GCCGATGCTCTTTTT	55159
rs183431280	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662878	AAAACAAACAGACAG[C/G]TTTAAGAATCTTCAG	55159
rs183435208	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647871	TGCTGGGATTATAGG[A/C]ATGGGCCACCGCGCC	55159
rs183448960	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74637402	GAAGCCAAGGCAGGC[A/G]GATCACCTGAAGTCA	55159
rs183469740	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633667	TAATACATATGTTCA[C/T]GGCCAAGCATGGTAG	55159
rs183629049	snp	A/C/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74631905	GATTACAGGCGTGAG[A/C/T]CACCACGCCTGGTCT	55159
rs183637505	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74646069	AAATATATTCTAAGA[C/T]AATTATATAAGATTG	55159
rs183715551	snp	C/T	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74647683	TGCAACTTCTGCCTC[C/T]CAGGTTCAAGCGATT	55159
rs183847692	snp	A/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74648517	GTGGCTCACACCTAT[A/T]ATCCCAGCACTTTGG	55159
rs183856608	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664705	ATTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG	55159
rs183881327	snp	A/G	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74635108	ACACGGTGAAACTCC[A/G]TCTCTTCTAAAAATA	55159
rs184088739	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74624688	AGGCGTGAGCCACCG[C/T]GTCTGGCCTCTAAAA	55159
rs184089737	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74660448	ACAGAGTGAGACGCT[A/G]TCTCAAAAACAAAAA	55159
rs184113825	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632273	TGCAGGCGCCTGTAG[A/T]CCTAGCTACTCGGGA	55159
rs184120574	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74646563	GAGGCCAAGGCAGGC[A/G]GATCATGAAGTCAGG	55159
rs184178765	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663693	ACAAATGCAAACAGG[A/G]TATGATATGCAAACC	55159
rs184243826	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641099	GCTAGACCTCTCTGC[A/T]GCATGGCTAATATTA	55159
rs184331575	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74660212	TGAACAAAGCCCTCT[C/G]TGAGCGGAGATCGCA	55159
rs184546549	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74642591	CTGCAGCCACAACCT[C/T]CTGGGCTCAAGAAAT	55159
rs184553027	snp	A/G	0.19459	0.243782	intron-variant	RFWD3	GRCh38.p7	16:74656324	AAAAAAAAAAAAAAA[A/G]AAAAAAAGAAAAGAA	55159
rs184576735	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74626199	GCAATCTCACATACA[C/T]ACATATGCGGATATG	55159
rs184612319	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643741	AGTGCAGTGGTGCAA[C/T]TTCGGCTCACTGCAA	55159
rs184709948	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657294	TGCCATAGAGCTCAA[C/T]GAGATTCGGCTGTTT	55159
rs184766282	snp	C/T	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74638970	CCATAATGAATACTA[C/T]AGGCAATGGTACTAT	55159
rs184773959	snp	C/T	0.00279162	0.0372561	intron-variant	RFWD3	GRCh38.p7	16:74652877	GTAGAGACAGGGTCT[C/T]ACAATGTTGGCCAAG	55159
rs184809029	snp	G/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74621830	CTCCCAAGTAGCTGG[G/T]ACTACAGGCATGCGC	55159
rs184847900	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634080	GTATACTTTAAATAT[A/G]TAGTTTACTCTCTGT	55159
rs184911869	snp	A/T	1.73006e-05	0.00294109	intron-variant	RFWD3	GRCh38.p7	16:74652150	AAAGACAACGGAATT[A/T]TAGTACAATGAACTA	55159
rs184940789	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621058	GCTGAAGCAGGCAGA[G/T]CACAAGGTCAGAAGT	55159
rs185013077	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638482	TCATAAAAGGACACA[C/T]TCACCAAGAATAACA	55159
rs185162873	snp	C/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74665071	GTCATCTTTGTTACT[C/G]AGGTTTCAATCAATG	55159
rs185190021	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635630	GGGAACATTAGGAAA[C/T]AGCTATTTTTCCAAT	55159
rs185267033	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74648712	GGGAGGCAGAGGTTA[C/T]TGTGGTGAGCTGAGA	55159
rs185268046	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74633220	AGGCGGAGGTTGTAG[A/T]GAGACAAGATTGCAC	55159
rs185276190	snp	C/T	0.00557542	0.0525036	intron-variant	RFWD3	GRCh38.p7	16:74647373	GCTCACCACAACCTC[C/T]GCCTCTCAGATTCAA	55159
rs185281089	snp	C/T	0.00580193	0.0535472	intron-variant	RFWD3	GRCh38.p7	16:74661477	AGTATTTGTAAAAAG[C/T]ATTAATAAAATAGAT	55159
rs185450678	snp	C/G	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74645813	GCTGGAGTGTAGCGG[C/G]AGAATCTCGGCTCAC	55159
rs185507870	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74666985	TTCTTCAATGGGTCC[C/T]CCGATAGCTGAAGCA	55159
rs185549193	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74649428	GTACACAGAACAGTA[C/T]AGTTAAGCCACAAGT	55159
rs185571565	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630716	ACCCACTGAAGAGAC[A/G]ATTAACACAATAATA	55159
rs185581804	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623771	ACAATCTGTAGTGTC[G/T]CAGTGACCTAGGGTC	55159
rs185585159	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74659749	CCATGAAAAAGAATG[C/T]TGAATCCAGATACAG	55159
rs185680132	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626721	AATATCACAGCATCA[A/G]TGAAATTTAGAACCG	55159
rs185697155	snp	A/G	0.00795532	0.062565	intron-variant	RFWD3	GRCh38.p7	16:74656536	CACCCAGGCTGGAGT[A/G]CAGTGGCATGATATT	55159
rs185796032	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662473	CAAGTAAGATGTCAA[A/T]AAACAAATACATGAA	55159
rs185822590	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74658677	TAGGTTATTCCCTTT[C/G]TGGAGACAGATTATG	55159
rs185827113	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643143	TATAGAGCTTTTTTT[C/G]TTTCTTTTAAAAAAA	55159
rs185861463	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74628774	CAGAGGAGGTTAAAC[A/G]CCTTTAGTCACTATC	55159
rs185861732	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643998	ACTGTTTTGTGCTTC[C/T]GAAATCCTGGTAATT	55159
rs185936802	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74639460	GGTCATTATGCAGCA[C/T]GTGACTGTAAAGTAA	55159
rs186062086	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623167	AAAAAACAAAATCTT[C/T]CCCACCGCTCAAACA	55159
rs186066800	snp	C/T	0.00398564	0.0444627	intron-variant	RFWD3	GRCh38.p7	16:74655115	TGTAGATGAAACACC[C/T]CTCTATTGGAAGATG	55159
rs186080651	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74653956	AATAGCAATCAAGTT[A/G]CTTTTCTTTTTTGGA	55159
rs186091240	snp	C/T	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74624503	TGGGTTCCAGCGATT[C/T]TCATGCCTCAGCCTC	55159
rs186107440	snp	G/T	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74640682	CAGTGGCTCATGCCT[G/T]TAATCCCAGCACTCT	55159
rs186339848	snp	G/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74637201	CATCCAGGCTGGAGT[G/T]CAGTAGTGCGATCAC	55159
rs186485884	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74654681	TGTCAAAAGCTGGGA[C/T]AGGCCAGAAGCCAGG	55159
rs186517643	snp	G/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74636240	CAAGGAACTAATAGG[G/T]AAAGGTGATTTGGTA	55159
rs186524383	snp	A/G	9.88517e-05	0.00702966	intron-variant	RFWD3	GRCh38.p7	16:74649205	CCTGCTAGTTGCTCT[A/G]CCAAGTCATTTCCAG	55159
rs186576909	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663861	GGGACTGTAAAAACC[A/G]GGTACCACAAAAGGC	55159
rs186610973	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634081	TATACTTTAAATATG[C/T]AGTTTACTCTCTGTC	55159
rs186613219	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74647938	CTAACCATATTCTGC[C/T]TGATTTTTTTTTAAT	55159
rs186680928	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667668	AAAGACGATCTAGAT[A/G]TAACAGAACTCACTA	55159
rs186692916	snp	C/T	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74640038	CTTTAGGTTTGTATG[C/T]ATAAGAAAAAACATA	55159
rs186719953	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637533	TCGAGATGCTGAGGC[A/T]GAGGCAGGAGAACCG	55159
rs186937203	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74650122	AACTATGTTGGTTTA[C/T]TGTTACATAAAACAT	55159
rs186991361	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74644949	TACTCTTAAATCTTA[C/T]AAAATTCTTGGATAC	55159
rs187006672	snp	A/G	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74646659	GGCATGACGGCGTGT[A/G]CCTGTAGTTCCAGCT	55159
rs187023169	snp	C/T	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74629484	GCCAATATGGTGAAA[C/T]CCCATCTCTACTAAA	55159
rs187222274	snp	C/T	1.64735e-05	0.00286993	missense	RFWD3	GRCh38.p7	16:74661116	ACGAAGATGCTGGGA[C/T]GGTGTGATTACCATC	55159
rs187224877	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74642361	ACTCCTGAGCTCAGG[A/C]GATCTGCCTGCCTCA	55159
rs187252203	snp	G/T	0.000115677	0.00760427	intron-variant	RFWD3	GRCh38.p7	16:74632506	CCAGTCTCCACCTAC[G/T]TCCCCAAATCACTCA	55159
rs187253398	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647621	CTTTGAGATGAAGTC[A/G]TGCTCCGTCTCCCAA	55159
rs187259014	snp	C/T	0.0209421	0.100162	intron-variant	RFWD3	GRCh38.p7	16:74625934	CTCACGCCTCTAATC[C/T]CAGCACTTTGGGAGG	55159
rs187300604	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74659197	GTGCTTGACCAAGAG[A/G]AATCCACTCTGCGTC	55159
rs187323613	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74629308	TAAAGGTAATCAAAG[C/T]AAACAAAAATAAAAA	55159
rs187456553	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74630257	TGTGCCACCACGCAT[A/G]GCTAACATTTTTTTG	55159
rs187463471	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74645731	CAGCCCATGATCATA[C/G]TCACAAATATTTTCT	55159
rs187471619	snp	A/C	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74659728	CAACATTAAAATCAG[A/C]AGGATCCATGAAAAA	55159
rs187573697	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641216	TGCCCAAGCAGGAGT[A/G]CAATGGTGCGACCTC	55159
rs187669549	snp	A/T	0.00835141	0.0640778	intron-variant	RFWD3	GRCh38.p7	16:74642970	ATTGTTTTTAAATAT[A/T]ATCACCCATTACAGC	55159
rs187676247	snp	C/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74656446	CCTCTAATGGATCTG[C/G]ACAAAGTAAATTGAA	55159
rs187763888	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651426	AGTTTATGACCAGCC[A/G]GGGCAACATGGAAAA	55159
rs187799764	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655243	CTTCAGTTGAAGCCG[A/G]TGCTCTTTTTTTTTG	55159
rs187808847	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651037	TCTAACAACTTACGA[C/T]AGTGATAAATGAGGT	55159
rs187816526	snp	A/C/G	0.00159617	0.0282053	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667992	GAGTTGAGCACAAGG[A/C/G]GAGCTATTCTCAAGC	55159
rs187833286	snp	C/G	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74624916	ATTGCTTAAGCTGAG[C/G]AGTTTGAGGCTACAG	55159
rs187844792	snp	A/G	0.00375668	0.0431767	missense	RFWD3	GRCh38.p7	16:74637950	GCCTGTTTCCTTAGC[A/G]TCTGTTCCTTCAGTA	55159
rs188045084	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656026	TTCATGTCTGTTAAT[A/G]TAACATATTCTGCAG	55159
rs188054354	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668569	AAAAGGGACGCTCCA[A/T]TCCTGTATGGATAAA	55159
rs188057720	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633578	CTGTAGTGACAAAAA[A/G]CAGTGACTGCTGGGG	55159
rs188082161	snp	C/T	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74659473	GCTGGTGCACGCCTG[C/T]AATCCCAGCTACTTA	55159
rs188164291	snp	C/G	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74636714	CTAGAGAACTGCAGA[C/G]TTTTTGTTTTTTTTT	55159
rs188176465	snp	A/C	9.88517e-05	0.00702966	intron-variant	RFWD3	GRCh38.p7	16:74649206	CTGCTAGTTGCTCTG[A/C]CAAGTCATTTCCAGA	55159
rs188186915	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74666590	AACCCAGATACGCGC[A/G]GGGGTTCGGGCTCCT	55159
rs188305981	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660326	GGTGTGGTGGCACGC[A/G]CCTGTAATGCCAGGT	55159
rs188342498	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74632004	GTTTCAAAGAAACAG[A/G]AAACATACAGTTTTG	55159
rs188344004	snp	G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646073	ATATTCTAAGATAAT[G/T]ATATAAGATTGTTCC	55159
rs188547357	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74657302	AGCTCAATGAGATTC[A/G]GCTGTTTTTCTTTAA	55159
rs188579410	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74628354	CGTTAGCCTGTGAGC[A/G]GTACCACAGCCACCC	55159
rs188583757	snp	C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664864	AGCAGAAATACAGAA[C/T]ACTTTTCTCGTCGCA	55159
rs188591436	snp	C/T	0.00557542	0.0525036	intron-variant	RFWD3	GRCh38.p7	16:74643820	AGCTGGGATTACAGG[C/T]GTCCGCCACTATGCC	55159
rs188598197	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74647835	GACCTCAGGTGATCC[A/G]CCCGCCTTGGCCTCC	55159
rs188802819	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659988	AAGCCTGGGGAGGTC[A/G]AGGCTGCAGTGAGCT	55159
rs188828770	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74660601	TAATTGTGCCCCCAG[A/G]TGGAATGCCAGTGAA	55159
rs188838047	snp	A/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631185	AGTTCTAAGGAAATA[A/T]AATAATAAATTAAAA	55159
rs188863468	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633811	GAGAATTAGCTGGGC[A/G]TAGTGGGGCGAGCCT	55159
rs189010602	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	RFWD3	GRCh38.p7	16:74621209	TTGAACCTAGGAGGC[A/G]GAGTTTGCAGTGAGC	55159
rs189090549	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74643249	GCCTCCCAAAGTGCT[A/G]GGATTACAAGAGTGA	55159
rs189118077	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74645837	GGCTCACTGCAAGTT[C/T]CGCCTCCTGGGTTCA	55159
rs189249656	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74626256	TTTTTGCTATATGAG[A/C]TTCTGTAAAAAAAGT	55159
rs189324874	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623604	CCTAGATGATGAGAG[A/G]ACACTCTCTAAGGTC	55159
rs189342781	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74654024	AAGTGTTCAATTCAG[C/T]GTTGTTTTTTTTTAG	55159
rs189356950	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74627558	CTGCCTCCTTTGTGT[A/C]TCACCTGACCAACAC	55159
rs189381128	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74656867	AACTCTTATGGATGA[C/T]TTTTGCCGGGCTCAA	55159
rs189501175	snp	A/G	0.00795532	0.062565	intron-variant	RFWD3	GRCh38.p7	16:74639063	TTTTTTTTTTAGCCC[A/G]AGTCTCACTCCATTG	55159
rs189508148	snp	C/T	0.00755907	0.0610114	intron-variant	RFWD3	GRCh38.p7	16:74652923	TGACCTCAAATGATC[C/T]ACCCACCTTGGCCTC	55159
rs189536063	snp	G/T	0.00438332	0.0466095	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622236	CTGAAACTAGGCCTG[G/T]GCAACCACTCTTAAT	55159
rs189614819	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74639484	AAAGTAAAAGGCTAG[C/G]CAGGATCTTTATGAA	55159
rs189654865	snp	A/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74635313	ATAAAAAATAAAAAA[A/T]AAAATTAACTAGGCA	55159
rs189867313	snp	A/C	0.00676944	0.0578265	intron-variant	RFWD3	GRCh38.p7	16:74646602	ACCATCCTGGCTGAC[A/C]TGGTGAAACCTCGTC	55159
rs189874663	snp	A/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74648535	CCCAGCACTTTGGGA[A/G]GCCGAGGTGGGTGGA	55159
rs189895715	snp	C/T	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74638592	AGAAAAAGATGAAAA[C/T]TGGAAAAGATAAAGC	55159
rs189976363	snp	C/T	0.00597247	0.0543191	intron-variant	RFWD3	GRCh38.p7	16:74633481	TACAATAAAAAATTA[C/T]GCAGCGAGAAAGAAG	55159
rs189982397	snp	C/T	0.00795532	0.062565	intron-variant	RFWD3	GRCh38.p7	16:74647583	GTGAGCCACTGCGCC[C/T]GGCCAACATTATTAT	55159
rs189990575	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74661841	TAATGCAGTATCTAA[C/T]TTTAGCAGGCAATAT	55159
rs190144334	snp	A/T	0.00473311	0.0484165	intron-variant	RFWD3	GRCh38.p7	16:74649112	ATAAATAGATTTTTT[A/T]AAAATGATGTTCATA	55159
rs190157405	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74632309	AGGCAGGAGAATGGC[A/C]TGAACCCGGAAGGTG	55159
rs190231823	snp	C/T	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74645020	AAAGAATAGCAGCTA[C/T]AAAATATTTAACTCA	55159
rs190235353	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74659509	CTGAGGCACAAGAAT[A/C]GCTTGAACCCGGGAG	55159
rs190265649	snp	C/G	0.00636936	0.0560724	intron-variant	RFWD3	GRCh38.p7	16:74629768	TGTTTGGCTCTCCTT[C/G]CTCTTTTTAATATAT	55159
rs190353731	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74654835	TGGTCTGGAAAGAAG[A/T]TCAAACCAGCCACAA	55159
rs190386378	snp	C/G/T	0.000878758	0.0209452	synonymous-codon	RFWD3	GRCh38.p7	16:74624048	TAGGTCCTGGAGCAA[C/G/T]GAGCCACTGGCAGCA	55159
rs190388738	snp	A/C	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74640447	ATGCGCCCGCCCGGA[A/C]ACTTAATTAAGGATA	55159
rs190405542	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74665352	AGCACTTTGGGAAGC[C/G]GAGGGCAGACCACTT	55159
rs190429582	snp	A/G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74635924	ATCAATTTACTCCCT[A/G/T]AATTCTCTTATTTGG	55159
rs190630324	snp	C/T	0.00478085	0.0486577	intron-variant	RFWD3	GRCh38.p7	16:74658853	GCTCACTGCAAGCTC[C/T]GCCTCCTAGGTTCAA	55159
rs190667525	snp	C/T	3.29457e-05	0.00405854	missense	RFWD3	GRCh38.p7	16:74644369	CCACCTACCTTTTCA[C/T]GCGCTCCTGTTCACT	55159
rs190869999	snp	C/G	0.00239393	0.0345281	intron-variant	RFWD3	GRCh38.p7	16:74655155	ACTTTTGCAGCTACA[C/G]AGAAGTCAATGCCTG	55159
rs190891314	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74655806	GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC	55159
rs190900374	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74659209	GAGGAATCCACTCTG[C/T]GTCCCCCAACAAGAA	55159
rs190915017	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74641091	ATTCCATTGCTAGAC[C/T]TCTCTGCAGCATGGC	55159
rs190933642	snp	A/G	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74629338	ATGAACATTACATAC[A/G]AATATTCTTTCCTTG	55159
rs191113065	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74651122	CAATTCATAATCCAA[C/G]AATATTCTTTCAGTG	55159
rs191123345	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668348	AAAAAACACAGGAAA[A/G]AAGAGTAGAAAGGGA	55159
rs191155100	snp	A/C/G	0.000578008	0.0169908	intron-variant	RFWD3	GRCh38.p7	16:74637976	CAGTAGGGAACTAGA[A/C/G]GGGGAAAGCCAGCAA	55159
rs191159926	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667034	GGTAGTTCGTCCTGA[A/C/T]GAGGCGGGACCGCGC	55159
rs191188267	snp	C/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74637385	TAATCCCAGCACTTT[C/G]GGAAGCCAAGGCAGG	55159
rs191357404	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648188	TGGCTAGACAGGACA[A/G]GTTATCCTCAATACT	55159
rs191363835	snp	A/G	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664537	AGGTAGCTGGAGACC[A/G]GGAGTTGGAGACCAG	55159
rs191393236	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74634567	TTAAGAAAAATTTTT[C/T]TTATAGCGATGGAGT	55159
rs191436539	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74649747	CAATCAGAATCCAAA[A/G]AAAGTCTCCATAATG	55159
rs191449969	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74647639	CTCCGTCTCCCAAGC[C/T]AGAGCGCAGTGACGC	55159
rs191693459	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74633649	ATAGGGAAACTTTTG[C/T]GGTAATACATATGTT	55159
rs191707618	snp	A/G	0.00318978	0.0398085	intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662474	AAGTAAGATGTCAAT[A/G]AACAAATACATGAAA	55159
rs191753473	snp	A/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74629003	ACATAAGAAAAGTCA[A/G]AAAAGAAACAAAGCT	55159
rs191975353	snp	C/G	1.64746e-05	0.00287002	missense	RFWD3	GRCh38.p7	16:74661224	TCAGGTCAACAGACA[C/G]TTGCGGAGCAGGCTG	55159
rs191987078	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667672	ACGATCTAGATGTAA[C/T]AGAACTCACTAATGA	55159
rs191990744	snp	A/G	0.00119737	0.0244387	intron-variant	RFWD3	GRCh38.p7	16:74642525	TATTTTTTTGAGACA[A/G]GTTCTTACTCTGTCA	55159
rs191995381	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74656096	ACACAGTGGCTCACA[C/T]CTGTAATCTCAGTAC	55159
rs191999436	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74632874	AATGCAGTGGCGTAA[C/T]CTCAGCTCACTACAA	55159
rs192028101	snp	A/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74626159	TCTACAAAGCAATAC[A/G]GAAAGCACGACTCAT	55159
rs192174357	snp	A/G	0.00676609	0.0577691	intron-variant	RFWD3	GRCh38.p7	16:74645939	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	55159
rs192237648	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638839	AAACATGTTGTTAGG[C/T]GATTTCGTCATGTAA	55159
rs192250164	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74652726	AACACTCCAAATATA[C/T]CTTGGCTGGCTGAGT	55159
rs192284087	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74659741	AGCAGGATCCATGAA[A/G]AAGAATGCTGAATCC	55159
rs192304232	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74646747	TAACTCAAAATTTAT[C/T]TGTATGATGGAATGC	55159
rs192311001	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74624603	GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTAGA	55159
rs192459969	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74625020	CAAACAAAAAGAAAT[G/T]AAAAATATTTTGAAG	55159
rs192477599	snp	C/T	0.00318978	0.0398085	intron-variant	RFWD3	GRCh38.p7	16:74633980	ACAGAACTAGATCTT[C/T]TGTCAAAAAAAAAAA	55159
rs192497566	snp	C/T	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74656493	ACCATTCTTTTTTTT[C/T]CTTTTTGGAGACAGG	55159
rs192513978	snp	A/G	0.00159617	0.0282053	intron-variant	RFWD3	GRCh38.p7	16:74660138	GCCTATGTAGAAAAC[A/G]GGGCAGATCCAGGCT	55159
rs192552585	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74631619	GTGACAGATAAAACG[C/T]TGTGACTAAGGGTAT	55159
rs192682187	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668654	CTATGGAAACCAACC[A/G]TGTAAATCCCTTCTC	55159
rs192703777	snp	C/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74638463	CATAACGAGGAACAA[C/T]GTATCATAAAAGGAC	55159
rs192767426	snp	A/C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74641325	GTGCCACCATGCCCG[A/C/G]CTAATTTTTGTATTT	55159
rs192806496	snp	A/G	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74648633	AAAAATTAGCTGGGC[A/G]GGGTGGCGTGTGCCT	55159
rs192891671	snp	C/G	0.0023933	0.0345097	intron-variant	RFWD3	GRCh38.p7	16:74651802	TATAAAACAGGAATC[C/G]ACAACATTTAGGGGA	55159
rs192954282	snp	C/G	0.00438332	0.0466095	intron-variant	RFWD3	GRCh38.p7	16:74630463	CTCACAGTGGGCCAA[C/G]AAAATACAACTAAGG	55159
rs193019283	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664932	CTTCCTAACCACTGT[A/G]GGCCAGTCGGAGGTG	55159
rs193035119	snp	C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74635366	CAACTACTTGGGAGG[C/G]TGAGGCAGGAGAATC	55159
rs193078789	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663063	GTGCCTGCCACCACG[C/T]CTGGCTAATTTTTTG	55159
rs193081005	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74642991	CCATTACAGCCACAC[A/G]TATAGATTTTGCCTT	55159
rs193183627	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74645791	AGACTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG	55159
rs193242124	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74626712	TGAAAGAACAATATC[A/G]CAGCATCAATGAAAT	55159
rs193252161	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74647839	TCAGGTGATCCGCCC[A/G]CCTTGGCCTCCAACA	55159
rs199513287	in-del	-/TC			intron-variant	RFWD3	GRCh38.p7	16:74639001	AATGGTATTTATGTA[-/TC]TAAACATAGAAAAGG	55159
rs199514598	snp	C/G/T	0.000399281	0.0141238	intron-variant	RFWD3	GRCh38.p7	16:74649102	AAATAAATAAATAAA[C/G/T]AGATTTTTTTAAAAT	55159
rs199536829	in-del	-/A	0.216048	0.247684	intron-variant	RFWD3	GRCh38.p7	16:74653491	AGAGACTCCATCTTC[-/A]AAAAAAAAAAGAAGA	55159
rs199557284	snp	A/C			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668618	TGTGGCAGTTTTTTT[A/C]TGTGTGTTTGGTCTA	55159
rs199613192	in-del	-/ATAA	0.0232847	0.105357	intron-variant	RFWD3	GRCh38.p7	16:74661888	CAACAGTTACAAGGG[-/ATAA]ATAGAGAAAGGACAT	55159
rs199617606	in-del	-/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622470	ATTTCTACAAAAAAA[-/T]TTAAAAAAGGAAAAA	55159
rs199648515	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621685	GGAATGGCATCAGGG[-/T]TTTTTTTTTGTTTGT	55159
rs199731609	snp	A/G	0.00199792	0.0315431	synonymous-codon	RFWD3	GRCh38.p7	16:74626370	TGCTGCTTCATCCCC[A/G]GTACACACCAGGATG	55159
rs199852515	snp	A/G	1.64849e-05	0.00287092	missense	RFWD3	GRCh38.p7	16:74632619	TGTTTGCCATGCATC[A/G]GAATGTACTGACTGC	55159
rs199873038	snp	C/T	0.000989647	0.0222226	intron-variant	RFWD3	GRCh38.p7	16:74626591	GCTGCACCATGGGGA[C/T]GCTACACAAAAAATT	55159
rs200006159	snp	C/T	0.000181203	0.00951675	missense	RFWD3	GRCh38.p7	16:74651965	CCTGGTCAACAACCC[C/T]TCCATACTCTGCAGA	55159
rs200105859	in-del	-/A	0.0126979	0.078662	intron-variant	RFWD3	GRCh38.p7	16:74657047	AGGCAGGCCCCAGGG[-/A]AAATGATTTAGGCTT	55159
rs200124008	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74634808	AGACAGCCAGAGAGG[-/A]AAAAAAAAGGGGGGA	55159
rs200183900	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74642956	ATTGTAATCAGTGAA[C/T]TGTTTTTAAATATAA	55159
rs200282348	in-del	-/CTC			intron-variant	RFWD3	GRCh38.p7	16:74655626	CTGTCTGTGCTCTCT[-/CTC]TTTTTTTTTGAGATG	55159
rs200352169	snp	A/G	1.64838e-05	0.00287083	missense	RFWD3	GRCh38.p7	16:74623962	TGGACCATCTTCTCT[A/G]TTAAGGTAGCCAAGT	55159
rs200354694	snp	C/T	8.23621e-05	0.00641672	missense	RFWD3	GRCh38.p7	16:74636408	CTCAGAGCATCACAG[C/T]ATGCCATGATCCGGC	55159
rs200387165	snp	C/T	4.94368e-05	0.00497152	synonymous-codon	RFWD3	GRCh38.p7	16:74661258	CAGGGGTGGTGTCGC[C/T]TGGCTGCTGATCACC	55159
rs200549419	snp	C/G	1.64743e-05	0.00287	missense	RFWD3	GRCh38.p7	16:74651962	CTGCCTGGTCAACAA[C/G]CCCTCCATACTCTGC	55159
rs200603961	snp	A/C/G	3.29464e-05	0.00405861	missense, synonymous-codon	RFWD3	GRCh38.p7	16:74626436	TTTGGTCAATAGTTT[A/C/G]CAAGTAGGTCCTCCA	55159
rs200669755	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74635472	ACTCCATCTCAAAAG[A/G]AAAAAAAAAAATCAA	55159
rs200695479	snp	C/T	1.64814e-05	0.00287061	missense	RFWD3	GRCh38.p7	16:74644626	CGTAATGCTGAGAGC[C/T]GGTGGTCCCCAGCAT	55159
rs200745293	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74659600	ACTCTTGTCTTAAAA[A/C]CAAAAAAAAAACCCA	55159
rs200766584	snp	A/G	0.00199792	0.0315431	intron-variant	RFWD3	GRCh38.p7	16:74649125	TTTAAAATGATGTTC[A/G]TATTACCTGTTTGGG	55159
rs200810849	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74630111	GCTATTTTTTTTTTT[C/T]TTGAGATGGCGTCTC	55159
rs200880591	in-del	-/TAGA			intron-variant	RFWD3	GRCh38.p7	16:74666183	ATTAGATAGACAGAT[-/TAGA]TAGATAGATAGATAG	55159
rs200891821	snp	G/T	1.65614e-05	0.00287757	intron-variant	RFWD3	GRCh38.p7	16:74632489	ACTCAACACCAAAGA[G/T]CCCAGTCTCCACCTA	55159
rs200898564	snp	C/T	0.000500242	0.0158073	intron-variant	RFWD3	GRCh38.p7	16:74636300	AAGGAAATAAATATA[C/T]GGAGTCTAATAAAGA	55159
rs200900059	snp	A/C	0.000116292	0.00762445	missense, intron-variant	RFWD3	GRCh38.p7	16:74630804	CTGAGCTACTAACTC[A/C]TGCACATGACTGCTC	55159
rs200915943	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74644823	AAATTAACAGAAGTG[-/C]AAAAAAAATGATACA	55159
rs200940067	snp	A/T			utr-variant-3-prime	RFWD3	GRCh38.p7	16:74622469	TATTTCTACAAAAAA[A/T]TTTAAAAAAGGAAAA	55159
rs200972788	snp	G/T	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74644448	GTGCCTGGCTTTCTT[G/T]TTGCACTAAAGAACC	55159
rs200985790	snp	A/C	1.66565e-05	0.00288583	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623901	ACATCTAACCAGCAG[A/C]ATGCCTTCAAGGTTT	55159
rs201011505	snp	C/G/T			intron-variant	RFWD3	GRCh38.p7	16:74656874	ATGGATGACTTTTGC[C/G/T]GGGCTCAAGACTTCA	55159
rs201070546	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74639038	CATTGAGCTAAGACT[C/T]TTTTTTTTTTTTTTT	55159
rs201075680	snp	A/G	9.88957e-05	0.00703122	missense	RFWD3	GRCh38.p7	16:74660975	CGGCTCTTGCCCTCC[A/G]TGAAGCAGATACCCT	55159
rs201145401	in-del	-/G			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74667128	ATGGGAGGTTTTTTT[-/G]GTTTTTTTTTTGTTT	55159
rs201176058	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74643683	TGTTTTTTTTTTTTT[C/T]TTTTTTTTTTGAGAC	55159
rs201194562	snp	A/G	0.000214149	0.0103455	missense	RFWD3	GRCh38.p7	16:74661229	TCAACAGACAGTTGC[A/G]GAGCAGGCTGGAGCA	55159
rs201232723	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74653232	TAGTTCCAGCTACTT[G/T]GGAGGCCAAGGTGGG	55159
rs201236333	snp	C/G	5.41726e-05	0.00520417	intron-variant	RFWD3	GRCh38.p7	16:74624077	CATCCCACAGCTAAA[C/G]AACACAAGCAGAGGG	55159
rs201251745	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74663377	GGAATGTGGTGTCTT[A/G]GAAAAACAATGTTTC	55159
rs201260391	in-del	-/TTTC			intron-variant	RFWD3	GRCh38.p7	16:74657475	CACCCAGGTTTTCTT[-/TTTC]TTTTTTTTTTTTTTT	55159
rs201286141	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74633294	GAAAAAAAAAAAAAA[C/T]AAAAGAAAAAAAAGT	55159
rs201326662	in-del	-/TCTTTA	0.0123036	0.0774623	intron-variant	RFWD3	GRCh38.p7	16:74666014	TATAACACCTTTTTC[-/TCTTTA]TAACAGGAAAAAGGG	55159
rs201326884	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74641840	CTGAGGCAGGAGAAT[G/T]GCTTGAACCTGGGAG	55159
rs201334831	in-del	-/GCC	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74647585	GAGCCACTGCGCCCG[-/GCC]AACATTATTATTACT	55159
rs201349753	snp	A/C/G/T			intron-variant	RFWD3	GRCh38.p7	16:74641960	AAAAAAAAAACCAAA[A/C/G/T]AAACCAAAAACCAAA	55159
rs201368423	in-del	-/G			utr-variant-3-prime, downstream-variant-500B	RFWD3	GRCh38.p7	16:74621703	TTTTTTGGTTTGTTT[-/G]TTTTTTTTTGAGATG	55159
rs201384422	snp	C/G	0.000431402	0.0146804	intron-variant	RFWD3	GRCh38.p7	16:74624090	AAGAACACAAGCAGA[C/G]GGAAGGGTCAGGAGT	55159
rs201418176	snp	A/G	0.000363895	0.0134839	synonymous-codon	RFWD3	GRCh38.p7	16:74628459	CTACTTACCAGGCCT[A/G]TAGGTCACAAGACAG	55159
rs201478620	snp	A/G	6.62592e-05	0.00575545	intron-variant	RFWD3	GRCh38.p7	16:74632484	ATGCTACTCAACACC[A/G]AAGAGCCCAGTCTCC	55159
rs201496518	snp	C/T	0.000182075	0.00953963	missense, intron-variant	RFWD3	GRCh38.p7	16:74630941	TATAAGTCTGGACCA[C/T]GGTATTTGTCTCCAG	55159
rs201539156	snp	A/G	0.000131822	0.00811748	missense	RFWD3	GRCh38.p7	16:74661256	AGCAGGGGTGGTGTC[A/G]CTTGGCTGCTGATCA	55159
rs201546947	in-del	-/T			intron-variant	RFWD3	GRCh38.p7	16:74640985	ATGAGAAATCTCTCC[-/T]TTTTTTTTTAAACAA	55159
rs201568694	snp	A/G	1.6651e-05	0.00288535	utr-variant-3-prime	RFWD3	GRCh38.p7	16:74623900	AACATCTAACCAGCA[A/G]CATGCCTTCAAGGTT	55159
rs201569043	in-del	-/TTTTTTTTTTTTT			intron-variant	RFWD3	GRCh38.p7	16:74643670	TGTTACTAGCAACTG[-/TTTTTTTTTTTTT]TTTTTTTTTTTGAGA	55159
rs201587155	snp	C/G/T	3.33735e-05	0.00408483	missense	RFWD3	GRCh38.p7	16:74661391	CCAGCAGGAGCTGGC[C/G/T]GTTGTTCGGCATGAT	55159
rs201677068	snp	C/T	3.3195e-05	0.00407387	missense	RFWD3	GRCh38.p7	16:74661350	CAGGCTGGAGGAGGG[C/T]TGGTCCCCCTTGGCT	55159
rs201749412	snp	A/C			intron-variant	RFWD3	GRCh38.p7	16:74659601	CTCTTGTCTTAAAAA[A/C]AAAAAAAAAACCCAG	55159
rs201817630	in-del	-/A			intron-variant	RFWD3	GRCh38.p7	16:74632087	ACACAGTCTCAGACC[-/A]AAAAAAAACAGAGCT	55159
rs201835275	snp	G/T			intron-variant	RFWD3	GRCh38.p7	16:74651004	TATTTACTAGTTTTT[G/T]GAGTAATTAGTTGGG	55159
rs201855350	snp	C/T	1.64743e-05	0.00287	synonymous-codon	RFWD3	GRCh38.p7	16:74651972	AACAACCCCTCCATA[C/T]TCTGCAGAGCTGTCA	55159
rs201859010	in-del	-/TG/TGAT			intron-variant	RFWD3	GRCh38.p7	16:74666219	GATAGATAGATAGAT[-/TG/TGAT]AGATTGATTAGATAC	55159
rs201896512	snp	C/T	0.00199792	0.0315431	missense, intron-variant	RFWD3	GRCh38.p7	16:74630916	CAGCTCCAGACAGGA[C/T]GTCCAGCATTATAAG	55159
rs201976767	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74649115	AATAGATTTTTTTAA[A/G]ATGATGTTCATATTA	55159
rs201999750	snp	C/T	0.000181188	0.00951636	missense	RFWD3	GRCh38.p7	16:74661074	GAAGTCTCTGCAGTC[C/T]GCTGATGAAGTTGGT	55159
rs202024128	in-del	-/TCTT	0.0263992	0.111815	intron-variant	RFWD3	GRCh38.p7	16:74655627	TGTCTGTGCTCTCTC[-/TCTT]TTTTTTTGAGATGGA	55159
rs202039346	snp	C/G	0.000319625	0.0126377	intron-variant	RFWD3	GRCh38.p7	16:74660895	TCATAATTTCTAGTA[C/G]AGCAATGATCACAGA	55159
rs202109867	snp	A/T			intron-variant, utr-variant-5-prime	RFWD3	GRCh38.p7	16:74662148	TAAACTAAAAAAAAA[A/T]ATTTTTTTTTGTTAT	55159
rs202114346	snp	C/T	1.64727e-05	0.00286986	missense	RFWD3	GRCh38.p7	16:74644407	AAAGCTCTCAGGGTT[C/T]GGGCATAAAGGACGA	55159
rs202130447	snp	A/G/T	6.60593e-05	0.00574682	missense	RFWD3	GRCh38.p7	16:74632641	ACTGACTGCTCTTCA[A/G/T]GTTGGCAGTACTCAA	55159
rs202136713	snp	A/G	0.00634392	0.0559617	intron-variant	RFWD3	GRCh38.p7	16:74624074	CAGCATCCCACAGCT[A/G]AAGAACACAAGCAGA	55159
rs202192869	snp	C/T			intron-variant, upstream-variant-2KB	RFWD3	GRCh38.p7	16:74664762	TAAAAAAAGAAAAAA[C/T]AAAGAAATAAAATAA	55159
rs202236091	in-del	-/C			intron-variant	RFWD3	GRCh38.p7	16:74665752	TTTCTTTCTTTCTTT[-/C]TTTCTTTTTTTGAGA	55159
rs367546101	snp	C/T			downstream-variant-500B	RFWD3	GRCh38.p7	16:74621015	CCGGGTGCGGTAGCT[C/T]ACGCCTGTAATCCCA	55159
rs367568231	in-del	-/T	0.00798231	0.0626693	intron-variant	RFWD3	GRCh38.p7	16:74643853	TTTTTTTGTATTTTT[-/T]AGTAGAGACGGGGTT	55159
rs367583924	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74658194	CTGTAGTCCTAGACT[C/G]CGTATGCTCCAGGAA	55159
rs367594828	in-del	-/TTC			intron-variant	RFWD3	GRCh38.p7	16:74665750	CTTTTCTTTCTTTCT[-/TTC]TTTCTTTTTTTGAGA	55159
rs367596958	snp	A/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74643967	CAGGCGTGAGCCACC[A/G]TGCCCGGCCCTAGCA	55159
rs367696930	in-del	-/A/AA			intron-variant	RFWD3	GRCh38.p7	16:74625199	GCAAGACCCTGTCTC[-/A/AA]AAAAAAAAAAAAAAG	55159
rs367756189	snp	A/T			intron-variant	RFWD3	GRCh38.p7	16:74632883	GCGTAACCTCAGCTC[A/T]CTACAACTTCTGCCT	55159
rs367955834	snp	A/C/G	0.000798403	0.0199641	intron-variant	RFWD3	GRCh38.p7	16:74643959	TGGGATTACAGGCGT[A/C/G]AGCCACCATGCCCGG	55159
rs367973085	snp	C/G	1.81886e-05	0.00301562	intron-variant	RFWD3	GRCh38.p7	16:74652170	ACAATGAACTATCAT[C/G]ACAAAAACAATCTAT	55159
rs367986631	snp	A/C/G	1.66946e-05	0.00288912	missense	RFWD3	GRCh38.p7	16:74661382	CTGGCCATGCCAGCA[A/C/G]GAGCTGGCTGTTGTT	55159
rs368052815	snp	C/T	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74656661	CAAGGTTTCAACATG[C/T]TGGCCAGGTTGGTCT	55159
rs368100720	snp	C/G	0.00199481	0.0315187	intron-variant	RFWD3	GRCh38.p7	16:74647975	TTTTTTATTGAGACA[C/G]GGTCTCACTCTGCTG	55159
rs368109000	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74660594	AATTAATTAATTGTG[C/T]CCCCAGGTGGAATGC	55159
rs368128720	snp	C/G			intron-variant	RFWD3	GRCh38.p7	16:74630147	GTTGCCCAGACTGGA[C/G]TGCAACGGCGCAATC	55159
rs368139616	snp	C/T			upstream-variant-2KB	RFWD3	GRCh38.p7	16:74668776	AAGAACATTCGTGTA[C/T]GCTTTTTGACTCCAA	55159
rs368209284	snp	A/G			intron-variant	RFWD3	GRCh38.p7	16:74639540	AGAAAACAGTGAACA[A/G]ATGGAAGGATATTAC	55159
rs368220807	snp	G/T	0.00358779	0.0422022	intron-variant	RFWD3	GRCh38.p7	16:74654253	TTTGTTGATCTTTTA[G/T]AAGAACCAACTTTTT	55159
rs368229682	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74661836	GCATATAATGCAGTA[C/T]CTAATTTTAGCAGGC	55159
rs368367533	snp	C/T			intron-variant	RFWD3	GRCh38.p7	16:74644798	ATCTTGAAGAAGATG[C/T]GCAACTAAGAAATTA	55159
rs368470574	snp	A/T	0.000153988	0.00877328	missense	RFWD3	GRCh38.p7	16:74628666	GGAGACCAGTGGGCA[A/T]CTGAAAGGAAAGTAA	55159

Page 1 | 2