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

RNF19B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs545034593	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32959407	AGATTAGCAACAGGA[C/T]ACTTGAGAGGAAAAC	127544
rs545119687	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32952882	TGCGCCACTGCACTC[C/T]AGCCTGGGTGACAGA	127544
rs545193336	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933315	GCTGGAGTGCAGTGG[C/T]GCAATCTCAGCTCAC	127544
rs545205658	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32932670	TTTTTGAAAGCTGGC[C/T]GCAAGCACTGCATCT	127544
rs545262721	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32941966	GCTGGGCGTGGTGGC[A/G]GGTGCCTGTAATCCC	127544
rs545555063	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32939338	GATTATGGGTTCCCA[A/C]CACCACACCCAGCTA	127544
rs545593870	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940056	AGCCTTTGCTTTGCT[A/G]CTCCAGCTTCAGGTG	127544
rs545690519	snp	A/T	0.00438332	0.0466095	intron-variant	RNF19B	GRCh38.p7	1:32957931	GAACTATGCTGCTCA[A/T]ATTTCTTATCTTTTT	127544
rs545706700	snp	C/T	0.000798403	0.0199641	synonymous-codon	RNF19B	GRCh38.p7	1:32964656	TAGCGATGTGGAGCG[C/T]GGCGACTCGGAGTCC	127544
rs545960275	in-del	-/T			intron-variant	RNF19B	GRCh38.p7	1:32949972	TGTGAGAAAGTAAAC[-/T]TTTTTTTTTTGAGAC	127544
rs546080660	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32958339	AAGCTTATTTCCTCA[A/C]AAAACATTTTTCTTT	127544
rs546269134	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32963712	GGCAGGGCGAGACTC[C/T]GTCTCCAAAAAAAAA	127544
rs546426525	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32950594	TCACTGTCACCCAGG[A/G]TGGAATGCAGTGGCT	127544
rs546468240	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32947263	TGTTGTGTTTCATTT[A/G]CACAATGAATGTTTG	127544
rs546492932	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32936376	AATTCAGGTCTAGAG[A/C]CTGTCAAAGATGGTG	127544
rs546505461	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32949967	TCCCATGTGAGAAAG[A/T]AAACTTTTTTTTTTT	127544
rs546710306	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963845	CCTCACCGAATGCTT[A/G]GCAGCCACCTCGAGC	127544
rs546715788	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966215	GGCTGGCGGATCACG[A/T]GGTCAGGAGATGGAG	127544
rs546728204	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965038	TCAGAGATCCTAGCC[C/T]GCTGCTCTCCCTGGT	127544
rs546836479	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32956393	AAATAACAACAACAA[A/C]AAAAATTAGCCGAGT	127544
rs546905864	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32934359	CCAGGACTAAGGTGA[C/G]AGAGGTCTGACACTG	127544
rs547048379	snp	A/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32943955	CTGTAAAATGCGCTG[A/T]ATTTTACTGATTTTT	127544
rs547068969	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951233	CAGTGTTGTATTTTT[C/T]AAAAAATCCAGGTTT	127544
rs547136338	snp	A/G	0.00358779	0.0422022	intron-variant	RNF19B	GRCh38.p7	1:32963742	AAAGAAAAAAAAAAA[A/G]AGATACTGTCCTCAC	127544
rs547267804	snp	C/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32963208	CTCCCGATAGCGTGG[C/G]ACAGAACACATAGTG	127544
rs547306474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955082	TTTATAACACTTACA[C/T]TATAATGTAACTAAC	127544
rs547434897	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32935892	AGCTGGGATTACAGG[C/T]GTGCGCAACTACCGC	127544
rs547461278	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32935065	TTGATCTCCTGACCT[C/T]GTGATTCACCCGCCT	127544
rs547539237	snp	A/C	0.0146672	0.084371	intron-variant	RNF19B	GRCh38.p7	1:32953983	GCGTGCTCTCGGCTT[A/C]CTGCAACCTCTGCCT	127544
rs547758754	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32944757	GCAGTGGCACGATCT[C/T]GGCTCACTGCAAGCT	127544
rs547817685	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32934855	TTTTATTTTGTCAGA[C/T]GGAGTCTCACTCTGT	127544
rs547822451	snp	A/G	1.67027e-05	0.00288982	intron-variant	RNF19B	GRCh38.p7	1:32943999	TAAATTCAAATGGAA[A/G]TAAACATCCTGCTTT	127544
rs547844664	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32937438	AGATGGAGGCTGGAC[A/G]TGGTGGCTCATGCCT	127544
rs548027627	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32942127	AAAAACAAAACAAAA[C/T]AAAACCATTGACAAT	127544
rs548042171	snp	C/T	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32954319	ACCCCAAATTACTCA[C/T]GAATCCACAGCAATC	127544
rs548042594	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32947868	GAGAGGCAACATGGA[C/T]GAAAGGCATTTAAGT	127544
rs548374041	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32947457	CTGAGGTTCGAGTTC[A/G]AGACCAGGCTGGCTA	127544
rs548477313	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32950220	TCAGGTGATCCACCC[A/G]CCTCGGCCTCCCAAA	127544
rs548539377	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32949267	CACAATGAAAGTTTT[G/T]AAAAAGCCCCTAGCA	127544
rs548606871	snp	A/C/T			intron-variant	RNF19B	GRCh38.p7	1:32944667	CATGTCCCAGCTAAG[A/C/T]GACCTTGGGAAAATT	127544
rs548661950	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32958213	CCTGGTGATCTAAAT[C/T]GGGGAAATTACATTA	127544
rs548701369	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32962302	GTTTGGTTAAGAAAA[C/T]AGATCAACAGTATCT	127544
rs548713281	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32961660	TGTTTATATATATAA[C/T]TATATATATGATTAT	127544
rs548730216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32953935	TTTTTTGAGACGGAG[C/T]TTCACTCTTGTTGCC	127544
rs548749132	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933731	ATCTCCTTTAACTCA[C/T]TTCTTCTTCTTCCTG	127544
rs548832356	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19B	GRCh38.p7	1:32935077	CCTCGTGATTCACCC[A/G]CCTTGGCCTCCCAAA	127544
rs548946419	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940486	AGGGATAGGCAGCTC[A/C]GTATCTACTAAAGTA	127544
rs548989847	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32960938	GGATCGCCTGAGCCC[A/G]GGAGATTGAGGCTGC	127544
rs548996236	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32960160	AAAATCCAAAACTCT[C/T]TGCTCTATCCTACAA	127544
rs549042746	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32935119	GCAGGTGTGAACCAC[C/T]GCGCCCAGCCCATTA	127544
rs549078017	snp	C/T	0.00358779	0.0422022	intron-variant	RNF19B	GRCh38.p7	1:32954441	CATGACATGAAGCTA[C/T]TAAAATCTCCAAACC	127544
rs549162001	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32934240	AGACTTGCCATCCTC[A/G]TTGTAGTAAAACACT	127544
rs549171786	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933490	TCGATCTCCCGACCT[C/T]GTGAGCCGCCCGCCT	127544
rs549551136	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32956267	AGCTACTCCCAGCTA[C/T]TCGGGAGGCTGAGGC	127544
rs549573829	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32949933	ACACACAAGCACATT[C/T]GACCAACTGTAAAAT	127544
rs549623904	in-del	-/CT	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32935871	TCCTGCCACAGCCCC[-/CT]GAGTAGCTGGGATTA	127544
rs549666934	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959443	AGTTACCTGACTTCG[G/T]GGTTTCTGAAAAGAC	127544
rs549673564	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32961041	AGATGCAAAGCCACT[A/C]GGCACATCCCAAGGG	127544
rs549749000	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32934364	ACTAAGGTGAGAGAG[A/G]TCTGACACTGGAAGC	127544
rs549749292	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32942079	TCCAGCCTGAGCCAC[A/C]GAGTGAGACTCTGTC	127544
rs549810777	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32941341	CAAGGTCAGGAGCTT[A/G]AGACCAGCCTGGCCA	127544
rs549824350	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32957815	CTCCAGCCTGGGCGA[C/T]AAAGCGAGACTCCAT	127544
rs549867181	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32939026	TATACATTTTATACT[C/T]CCATGACTTTGCACA	127544
rs549871090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32949299	AACAAAATGAACTAA[C/T]TGCTCTCCAATCTGA	127544
rs550145010	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32953042	TGTGATGATAGCTCA[C/T]TGCAACCTGAAACTC	127544
rs550463748	in-del	-/C	0.00795532	0.062565	intron-variant	RNF19B	GRCh38.p7	1:32958456	GCGTGGTGGCTCACG[-/C]CTGTAATCCCAGCAC	127544
rs550559809	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966348	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG	127544
rs550597966	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32958066	ATGAGCTCTCAATCT[A/G]TTCAGAGCATAAGGT	127544
rs550651137	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32940604	TCATCTTAATCTACC[C/T]TTTGGTATGAGGCAT	127544
rs550750506	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32945726	ACTTGTAAGTTATCT[A/G]TATTAAAACATATCC	127544
rs550835302	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32938704	TCTCTTAAATATCTA[C/T]TGAAATCGTCCCCTC	127544
rs550850978	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32961335	CATCCTCAATAATGC[A/C/G]GCTATGTTGACAAGC	127544
rs550851157	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964875	CCGCTGCCCTGCGCA[A/G]GCGCTTCGCTCAAAC	127544
rs550989415	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951265	TGCAGGTTACTCTAT[C/T]TACATCTGGGAGCAG	127544
rs551120693	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959572	TCCTTTATAAAATGC[A/T]CGCCAATATCCACCT	127544
rs551231662	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32937574	ATTAGCTGGGCATGG[A/T]GGCACGTGCCTGTAG	127544
rs551373168	snp	G/T	0.000115434	0.00759631	intron-variant	RNF19B	GRCh38.p7	1:32938382	CCTCTCCTGGACATC[G/T]GACTGTTCACATACC	127544
rs551380350	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967212	CTCAAATAGGAAGGA[A/G]GTTTGATGCTGGATG	127544
rs551541921	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32939687	CCAATAGTGTCTCAG[A/G]GCCCATAACTATTGC	127544
rs551594746	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32958383	TAACATACCTTAGGA[A/T]ATAGTGATGTGAGTG	127544
rs551653328	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951943	GGGATTACAGGCGCC[C/T]GCCACCACGCCCGGC	127544
rs551653563	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32958707	CCTGGGCAACAGAGC[A/G]AGACTCCATCTAAAA	127544
rs551665374	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32958137	TGGTAACTATTAAAG[A/G]AGTTTAGGGAAAGTT	127544
rs552031207	snp	C/T	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32950980	TAGTAGCTGGGACTA[C/T]AGGCATGCATCACCA	127544
rs552055306	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966118	AAAGGGAAGAAAGAT[A/G]CATCCTCTTCCTTTT	127544
rs552137429	snp	A/G	0.000199435	0.00998387	intron-variant	RNF19B	GRCh38.p7	1:32938540	TAACCTGTGTAAAGA[A/G]GGGACGTTCAAGTTA	127544
rs552148915	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32944814	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	127544
rs552394028	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963165	CCCTCACCCTACCCA[A/C]GGCAGCAAGGTAAGA	127544
rs552434576	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32950881	GAGTCTCGCTCTGTC[A/G]CCAGGCTGGAGTGCA	127544
rs552436461	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32957422	TAATTTTCTATCTAT[C/T]TATGTATCAATTATC	127544
rs552541890	snp	A/C	0.0023933	0.0345097	intron-variant	RNF19B	GRCh38.p7	1:32943440	CACGGTGAAACACCA[A/C]ACCCCGTCTATACTA	127544
rs552640875	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32951384	GCAGCAGGAGCAGCA[A/G]CTCTTCTTGCAGGAG	127544
rs552661380	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966833	GGAGGAATGCTTGAG[A/C]CTGGGAGGTTGAGAC	127544
rs552667791	snp	A/G/T	0.000231054	0.0107459	synonymous-codon	RNF19B	GRCh38.p7	1:32964206	CTCGGGGCAGCTGAT[A/G/T]GGCACCCTGCTCTCG	127544
rs552701175	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19B	GRCh38.p7	1:32956344	ATTGCACCACTGCAC[C/T]CCAGCCTGGGTGACA	127544
rs552764690	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32944249	CATGGACAAACCACT[G/T]TATAAAGAAAGGAAG	127544
rs552790830	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32935772	GAACTCTTTTTTTTT[G/T]GAGACAGGGTCTCTG	127544
rs552794807	snp	C/T	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32957774	GAGAGGCAGAGGTTG[C/T]AGTGAGCTGAGATGG	127544
rs553218814	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32963489	GGGAGGCCGAGGCAG[A/G]AGGATCACCTGAGGT	127544
rs553397475	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32959854	CATCCTAGCTAACAC[A/G]GTGAAACCCCGTCTC	127544
rs553400236	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32962742	GACTCCCCAGCATCT[C/T]TTTGTCGCCAAAACA	127544
rs553432606	snp	C/T	0.00279162	0.0372561	intron-variant	RNF19B	GRCh38.p7	1:32950424	AAGTTTCATAAATAA[C/T]AGGGTACAAAACTAT	127544
rs553459171	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32944233	TTCTTCCCAGTCTGG[G/T]CATGGACAAACCACT	127544
rs553467730	snp	C/G	0.0023933	0.0345097	intron-variant	RNF19B	GRCh38.p7	1:32935284	CTGGAATTACAGACA[C/G]ATGCCACCAGGCCTG	127544
rs553502850	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32942860	AAGCTAGAAAAACCG[G/T]CCGGGCGCGGTGGCT	127544
rs553522128	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32943701	TAAAAAGCAAGTGAG[A/G]TAATTGTGTAAAATA	127544
rs553527164	snp	A/G	0.00478085	0.0486577	intron-variant	RNF19B	GRCh38.p7	1:32943034	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	127544
rs553579240	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954570	ATGGTGAAATCCCGT[C/T]TCAACTAAAAATACA	127544
rs553632951	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32955333	TCTATTGGCTTATTA[C/T]ATGCCAGGTACTATA	127544
rs553769958	snp	C/T	0.00557542	0.0525036	intron-variant	RNF19B	GRCh38.p7	1:32935020	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	127544
rs553839383	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954053	AGCTGGGCTTACAGG[C/T]GCCCGCCACCATGCC	127544
rs554312239	in-del	-/TTTTTCT	0.0023933	0.0345097	intron-variant	RNF19B	GRCh38.p7	1:32953122	CCATGCCCAGCTAAC[-/TTTTTCT]TTTTTCTTTTTATTT	127544
rs554351062	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32951025	TTGTATTTTTGTAGA[C/G]ATAGGGTTTCACCAT	127544
rs554386708	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940681	GGCAACCATCTCCTC[C/T]ACCTTCCTATCCTGC	127544
rs554396501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32935419	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC	127544
rs554457888	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32943119	GCACTCCAGCCTGGG[C/G]AACAGAGCAAGACTC	127544
rs554470629	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933563	CCCGGCCAAGCTATT[C/G]TAACTTTTCTAATGC	127544
rs554494189	snp	C/T	6.63449e-05	0.00575917	intron-variant	RNF19B	GRCh38.p7	1:32949530	GCTCACATCATGAAA[C/T]ACCAAATAAAGAGAC	127544
rs554530028	in-del	-/TTT	0.00438332	0.0466095	intron-variant	RNF19B	GRCh38.p7	1:32961976	CTATGCAGTGTTTTG[-/TTT]TTTTTTTTTCTTGAG	127544
rs554753485	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955176	CTCAGTCTAGTATAC[C/T]GGTTCATGCTCAAAA	127544
rs554855194	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32945343	GCACACTCTGATAAT[C/T]TGGTGTGCTTGAAAA	127544
rs554965507	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32961144	CTCAAAACACCGTGT[A/G]AACATTAATTAAACC	127544
rs555045516	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32948954	GACAATTTAGGAAAT[C/T]ATGCTGTGCCAGGAA	127544
rs555056521	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954655	AGGCAGGAGAATTGC[C/T]TGAAACTGGGAGGCG	127544
rs555233759	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959177	AGGCCAATAGCTGAT[A/G]CTGTTTCCTGGGATC	127544
rs555384949	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32939829	GAACTAGAACAGCTG[G/T]ACTGGCTAAGCTGCA	127544
rs555409973	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19B	GRCh38.p7	1:32954836	CTAAACACGTTCTAA[A/G]ACTGCATGTGAGACC	127544
rs555520858	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32963613	ATCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG	127544
rs555566031	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32945220	ATTTCATGGCAAGTA[A/G]AGAAGGAAGATGAAA	127544
rs555623916	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32953208	GGAACTTCTGTCTTC[A/G]AGCAACCCTCCCGCC	127544
rs555636226	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959635	AGATTATAGTCTGAA[C/G]ACTATAAAGAACTAT	127544
rs555911787	snp	A/C	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32960218	TGAATGTATGGTGTT[A/C]TTGTTATTATGAGTA	127544
rs555922824	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32948668	TTCCAAGAAAAATGA[A/G]ATTTCTACCAGTCGA	127544
rs555923481	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32952690	GAGGTTGCAGTGAGC[A/C]GAGATTGCGCCACCA	127544
rs555954216	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32952157	TAATGTCGACCATTT[A/C]TTGTAGTTCATGTTC	127544
rs556222168	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959760	TAATAATGTGAGGCC[A/G]GGCACAGTGGCTCAC	127544
rs556239807	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966850	TGGGAGGTTGAGACT[A/G]CAGTGAGCCGTGATT	127544
rs556375954	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32939141	CCTCATTATCCCAGC[A/G]AACCATTCACTTCTT	127544
rs556398043	snp	G/T	0.00914312	0.0669923	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933269	ATTATTTTTTTTTTT[G/T]TGTGAGACGGAGTCT	127544
rs556400227	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940550	TCCCTATATTCTCTA[C/T]ACTGAACCAAAATTA	127544
rs556417368	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32948028	AGTCCAGACTACCTG[C/T]AATATGGCAAGCAAA	127544
rs556462804	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32939986	CATGAGATGCACAGA[C/T]GGGTCAGTAGCAGCC	127544
rs556699564	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32941250	CAAAGCCCACTATCA[A/G]TAAACCATGATGGGC	127544
rs556754322	snp	C/G	2.09238e-05	0.00323442	intron-variant	RNF19B	GRCh38.p7	1:32946614	TTACAAATACAGCTA[C/G]TATTATCATAGGGCT	127544
rs556779851	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32946089	CAGGCTGGTCTCAAA[C/T]ACCTGGGCTCAACTG	127544
rs556790327	snp	C/T	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32952256	TTCCAAATATGTCAA[C/T]TAAGCGCTCAGATTA	127544
rs556834434	in-del	-/AGA	0.00835141	0.0640778	intron-variant	RNF19B	GRCh38.p7	1:32937934	TACCATGCCACAAGT[-/AGA]AGAAGCCAGAATACC	127544
rs557016435	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32952610	AGCTGGGCATGGTGG[C/T]GGGCGCCTGTAATCC	127544
rs557088998	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32934745	TGACTCATACAAAGT[A/C]AGTCACTCTAAGATT	127544
rs557097213	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963298	GTCAGGGAGAACACG[C/T]CTTCTTCTGCAATGC	127544
rs557106571	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32957097	AGAAAAAAGAAAAAA[A/T]GTGCTTCAACCCAAA	127544
rs557237874	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32940220	CCTACTTAGGTGGTT[A/G]TCAGATGCTGGTTCA	127544
rs557271457	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965317	AATAAAACAGACAAG[A/G]TCCCCTATTGCAAGG	127544
rs557370477	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32950987	TGGGACTATAGGCAT[C/G]CATCACCATGCGCAG	127544
rs557452277	snp	G/T	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32944960	CCCAAAACACTGGAA[G/T]TACAGGCGTGAGCCA	127544
rs557503463	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32956087	ACACAAAAATTAGGC[C/T]GGGCATGGTGGCTCA	127544
rs557521477	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32940073	TCCAGCTTCAGGTGC[C/T]CTTCAAAAATGTGCC	127544
rs557643977	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32950488	TAGTATTTGTTTATA[C/T]GAAGGAAGAGGACAT	127544
rs557816364	snp	C/G	0.00318978	0.0398085	intron-variant	RNF19B	GRCh38.p7	1:32952649	CAGGAGGCTGAGGGA[C/G]GAGAATCGCTTGAAC	127544
rs557840877	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32947425	AGAACTTTGGGAGGC[C/T]GAGGCAGGCGGACCA	127544
rs557845295	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32955027	TATACTTAACCTCTC[G/T]AGGCAGCTCGTTGCC	127544
rs557900699	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951051	ACCATGTTGGCCAGG[A/C]TGGTCTCGATCTCTT	127544
rs557904217	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32953094	TCAGGCCTCCAAGTA[C/T]CAGTGCATACCACCA	127544
rs558088711	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32958381	TATAACATACCTTAG[A/G]AAATAGTGATGTGAG	127544
rs558163201	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32945055	GATTAAATAAATTAA[C/T]ATATGCAAAAGTCTC	127544
rs558223946	snp	A/C	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32956808	TAAAGAAATGTGTTC[A/C]TATATTATGTCTGTA	127544
rs558243980	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	RNF19B	GRCh38.p7	1:32932239	AGATGAGCAATTAGG[A/C]GGCCACTACAGGTTG	127544
rs558375337	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963399	CTTGGCCAAATATCC[C/T]CTCCCCACTCTCATT	127544
rs558445906	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32936028	TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC	127544
rs558589728	snp	A/C	0.00438332	0.0466095	intron-variant	RNF19B	GRCh38.p7	1:32947484	GCTAACATGGTGAAA[A/C]CCCGCCTCCACTAAA	127544
rs558600798	snp	A/C	0.000399281	0.0141238	synonymous-codon	RNF19B	GRCh38.p7	1:32964170	CAAGCGGATGTCGTG[A/C]GGGTTGAGTCGCTCG	127544
rs558778690	snp	C/T	0.0023933	0.0345097	intron-variant	RNF19B	GRCh38.p7	1:32950279	TGCCTGGCTATAAAT[C/T]TCTTGAGATTCCAAA	127544
rs558887118	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32950756	TGCCCAGGCTGGTCG[C/T]AAACTTCCGGGCTCA	127544
rs558962328	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955330	GTATCTATTGGCTTA[C/T]TATATGCCAGGTACT	127544
rs558998007	snp	A/G/T			intron-variant	RNF19B	GRCh38.p7	1:32962600	CTCCTTTTGAAAGGA[A/G/T]ACAACCAGCAGCATC	127544
rs559005397	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32943224	CTACGTTACTTACTA[C/T]GAGTAGAAACCACAT	127544
rs559014345	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32944712	TTTTTTTTTTGAGAC[A/G]GAGTCTCACTCTGTT	127544
rs559015539	snp	A/G	5.0424e-05	0.0050209	intron-variant	RNF19B	GRCh38.p7	1:32949787	TAACTAGGTAAGGAA[A/G]CAGTAAGAGATACCA	127544
rs559024063	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951061	CCAGGATGGTCTCGA[A/T]CTCTTGACCTTATGA	127544
rs559032442	in-del	-/TTCT			intron-variant	RNF19B	GRCh38.p7	1:32938990	CATAGTCACTCTGAA[-/TTCT]TTCTTTCTTTAAATA	127544
rs559101589	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955912	GAAGCTAAAAGAAAG[A/G]TGTAGAAAATTACAT	127544
rs559155701	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32935121	AGGTGTGAACCACTG[C/T]GCCCAGCCCATTATT	127544
rs559264636	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32957074	TGCTTAAAATCCTTC[A/G]AAGAAAAAGAAAAAA	127544
rs559335101	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32961208	ATAAGAAAAATAACG[C/T]AGGTAGGAGGCTGTT	127544
rs559448951	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32962248	TGCTAGGACTATAGG[C/T]GTGAGCCACCGAGCC	127544
rs559655716	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954828	AAACGTAGCTAAACA[C/T]GTTCTAAAACTGCAT	127544
rs559969416	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32958590	GCATGGTTGCAGGTG[C/T]CTGTAGTCCCAGCTA	127544
rs560091316	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32949204	GGCACTTAAGTCAGC[C/T]TGAAGGCAAACAGCA	127544
rs560139438	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32934576	ATCCCAGCTACTTGG[G/T]AGTCTGAGACTTGAG	127544
rs560205377	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32947636	TGCACTCCAGCCTGG[A/G]CGACAGAGAGAAACT	127544
rs560212616	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32934709	AAGATCTGAAAGTTG[G/T]GGAAGTTAGGGGCAT	127544
rs560257070	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32955992	CCCAGAACTTTGTCA[C/G]GCAAAGGCAGGAGGA	127544
rs560265769	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954404	GGTACCTGGTCTGAG[A/C]TCTTGCCTCTGACTC	127544
rs560326751	snp	C/T	0.00279162	0.0372561	intron-variant	RNF19B	GRCh38.p7	1:32941154	CCTGAGTCCAGGAAG[C/T]TGAGGCTGCAGTGAG	127544
rs560590189	in-del	-/AAC	0.0011988	0.0244533	intron-variant	RNF19B	GRCh38.p7	1:32956382	ACTCTCTCTTCAAAT[-/AAC]AACAACAACAAAAAT	127544
rs560689578	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32961976	CTATGCAGTGTTTTG[G/T]TTTTTTTTTTTCTTG	127544
rs560717833	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32942803	AGATTTAAAAAATAT[G/T]TTTGGGTCATGTGCT	127544
rs560816498	snp	C/G	0	0	intron-variant	RNF19B	GRCh38.p7	1:32959412	AGCAACAGGATACTT[C/G]AGAGGAAAACATTAC	127544
rs561046019	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32942053	AGTGAGCCGAGATCA[C/T]GCCATGGCACTCCAG	127544
rs561192883	in-del	-/A	0.00318978	0.0398085	intron-variant	RNF19B	GRCh38.p7	1:32941748	ATGGAAAGAACAATG[-/A]ACTTTGCATAACTGA	127544
rs561285853	snp	A/G	0.00318978	0.0398085	intron-variant	RNF19B	GRCh38.p7	1:32959467	AAAAGACATACTTGG[A/G]CAGAGACTCAAAAGC	127544
rs561557468	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32932745	AATTTCCTTGTCTTC[A/G]GAGTTGTTTGGCTAA	127544
rs561633352	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32941032	GTTTAAGACCAGCCT[A/G]GGTAACCGAGCAAGA	127544
rs561673453	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32959976	GAATGGCGTGAACCC[A/G]GCAGGCAGAGCTTGC	127544
rs561695103	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940235	GTCAGATGCTGGTTC[A/G]TGCAACGGCTGTGCT	127544
rs561698403	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964811	GCCCTCCCGGCGATA[A/G]AAGCCGAGCGGCAAC	127544
rs561885266	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965679	GATTGAAATTTATTT[A/T]TTTTTTTTCCTGAGA	127544
rs561889526	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32958857	GGCAGGGGAGTGATA[C/T]AGATGTTCTCCTTTA	127544
rs561895068	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32952374	TGAGGCAGGAAGATC[A/G]CTTGAGGCCAGCATT	127544
rs561974075	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32946170	AACCATCATGCCTGG[C/T]CCAGCATTCTACCTT	127544
rs561976082	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32957345	TCATGCAAATTCTAT[C/T]GTTCTTTCATCTATC	127544
rs562028323	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951681	TTCCATACTTTTTCA[A/G]TTCAAACCTATACCT	127544
rs562171436	snp	A/G	0.00159617	0.0282053	intron-variant	RNF19B	GRCh38.p7	1:32937360	GAATTTCAAAAAGAT[A/G]GGTGAACAGTTAACT	127544
rs562186303	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32947614	CAGTGAGTCGAGATC[A/G]AGCCACTGCACTCCA	127544
rs562198778	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32958577	AAAAATTAGCCAGGC[A/G]TGGTTGCAGGTGCCT	127544
rs562418000	snp	A/C	0.00636936	0.0560724	intron-variant	RNF19B	GRCh38.p7	1:32938141	ATAGCCAAGAAAGAC[A/C]AAAAAAAAAAAAAAA	127544
rs562500848	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32958641	GAATAGCATGAACCC[A/G]GGAGGTGGAGCTTGC	127544
rs562560286	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965833	GCCACCAGGCCTGCC[G/T]ATTATTTTTATTTTT	127544
rs562770247	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933413	GCGCCCACCACTACG[A/C]CCGGCTAATTTTGTG	127544
rs562873242	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964910	CACAACCCTTGCGCC[A/C]CGGTCTAGGAGTGCG	127544
rs562983603	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32952821	GGGAGGCTGAGGTGG[A/G]AGGACTGCTTGAGGC	127544
rs563050858	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32937464	TGCCTATAACCCCAG[C/T]GCTTTGGGAGGTCGA	127544
rs563065775	in-del	-/AC			intron-variant	RNF19B	GRCh38.p7	1:32947292	TGTTTGTAAATATTA[-/AC]ACATTTTGTTTATTT	127544
rs563108510	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32944784	AGCTCCGCCTCCCAG[A/G]TTCACGCCATTCTCC	127544
rs563380734	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933431	GGCTAATTTTGTGTA[C/T]TTTTAGTAGAGACGG	127544
rs563406393	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32960349	ATTTGGCTGGCAAGA[A/G]CTTTATCTGTGGGCA	127544
rs563489979	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963159	GTCTACCCCTCACCC[C/T]ACCCAAGGCAGCAAG	127544
rs563494423	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32935109	TGCTGGGATTGCAGG[C/T]GTGAACCACTGCGCC	127544
rs563691976	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32955318	CAATGTATCCATGTA[C/T]CTATTGGCTTATTAT	127544
rs563704308	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32949891	CACATATGATACAGA[A/G]AAAAGAATACACATA	127544
rs563709120	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32936240	AGCTAATAATTCTTC[A/C]GCCTGACTACAAAGT	127544
rs563956267	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32938582	GGGTATTCCAAGACA[A/G]TCTGCTTCCTGGCAC	127544
rs563970326	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32935729	GAATATTCTGTTCTC[C/T]AACTTGTAACCATGC	127544
rs563970377	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32943802	GGAGTTACTTGGATT[C/T]CTACTAGTTTGTACC	127544
rs564136502	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32946133	GGCTTCCCAAAGTGC[A/T]AGGCCACGTATTACA	127544
rs564261948	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32957614	TGAGGCGGGTGGCTC[A/G]CTTGAAGTCAGGAAT	127544
rs564366235	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32952322	ATTTTAGCCAGGTGA[C/G]ATGGCTCATGCCTGT	127544
rs564385922	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32935046	CATGTTGGCCAGGAT[A/G]GTCTTGATCTCCTGA	127544
rs564469795	snp	A/G	0.0023933	0.0345097	intron-variant	RNF19B	GRCh38.p7	1:32963723	ACTCCGTCTCCAAAA[A/G]AAAAAAGAAAAAAAA	127544
rs564507365	snp	A/T	0.00953873	0.0683987	intron-variant	RNF19B	GRCh38.p7	1:32955579	TACAAAAAAAAAAAA[A/T]ACAAAAATTAGCTAG	127544
rs564554116	in-del	-/T			intron-variant	RNF19B	GRCh38.p7	1:32953140	TCTTTTTTCTTTTTA[-/T]TTTTTTTTTTGTAGA	127544
rs564554639	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32943898	AAAAATACTTTACCC[C/G]CTACAAAGCTCATTA	127544
rs564588850	snp	C/T	0.00438332	0.0466095	utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964746	CTCCCGCCTCAGCGC[C/T]CCTCAGCCAGCGCCC	127544
rs564643392	snp	A/G	0.00318978	0.0398085	intron-variant	RNF19B	GRCh38.p7	1:32949958	TAAAATATATCCCAT[A/G]TGAGAAAGTAAACTT	127544
rs564810170	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32944442	TGTGTTTTGCACAGT[A/G]AATATATGTTGCTTT	127544
rs564978918	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965001	GTCAGGTGGTTCCAG[A/G]GCCGCCATGTTGCGG	127544
rs565104889	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32949108	TGAATGTGTGACATT[C/G]CTCCTTTTAAGGTTA	127544
rs565149251	snp	A/G			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32934034	ATAATTTGCGTTTCA[A/G]AGATCTCCAGGCTGT	127544
rs565217910	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32937409	AAATAACATTTTAAT[C/G]TAACACTCAAATGAG	127544
rs565243032	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32942705	ACTTGTCCAAGGCCA[G/T]GGTAGTTACATGAAA	127544
rs565301074	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32943506	CTGTAGTCCCAGCTA[C/T]TCAGGAGGCTGAGGC	127544
rs565641579	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32935896	GGGATTACAGGCGTG[C/T]GCAACTACCGCCTGG	127544
rs565656369	snp	G/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32934195	CTGCAGTGCCCAAGA[G/T]ATAAGAATCTTCTAA	127544
rs565700285	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955104	GTAACTAACTGTTTA[C/T]ATGCTTGCCTTCCAA	127544
rs565761687	in-del	-/AATAATAATAAT	0.00159617	0.0282053	intron-variant	RNF19B	GRCh38.p7	1:32960835	GACCCTATCTCTACA[-/AATAATAATAAT]AATATTAATAATAAT	127544
rs565997918	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32956424	GTGGTGGGGCGCGGT[A/G]GCGTGTGGTGGCACA	127544
rs566015022	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955673	AGGACGGCTACAGCC[C/G]GGGAGGTGGAGGCTG	127544
rs566236274	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32934894	CTGGAGTGCAAAGGC[A/G]CGATCTCGGCTCACT	127544
rs566392361	in-del	-/TT	0.00318978	0.0398085	intron-variant	RNF19B	GRCh38.p7	1:32945197	ACAAAAGTAATTTTG[-/TT]TTGTGGATTTCATGG	127544
rs566426204	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32953181	GTCTTGCTATGTTGC[C/T]CAGGCTGGTCTGGAA	127544
rs566431105	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32948445	TTCCTAGGAGTATAT[A/G]TAAGAAATGAGGCAG	127544
rs566475201	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959573	CCTTTATAAAATGCA[A/C/T]GCCAATATCCACCTG	127544
rs566550658	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32947899	GGCTCTTAAAAGATA[A/G]GAACTGAACAAGTTG	127544
rs566569623	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32956794	TAGACTTCAGTGGTT[A/G]AAGAAATGTGTTCCT	127544
rs566581737	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933476	TAGCCAGGATGGTCT[C/T]GATCTCCCGACCTTG	127544
rs566609018	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32953743	GTTATTTTGCATTAA[A/G]TGGGAAAGTTACTGG	127544
rs566799221	snp	G/T	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32945853	TAACTCCAGCAGAAT[G/T]AAGTAAGCATTTTAC	127544
rs566801327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32952566	GCCAACATGGTGAAA[C/T]GCTGTCTCTACTAAA	127544
rs566839678	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940426	TCTGTTGCTTGAATC[C/T]TTCTTATAGCCAAAT	127544
rs566864415	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32951951	AGGCGCCCGCCACCA[C/G]GCCCGGCTTTTTTTT	127544
rs566890688	in-del	-/TA	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32935661	AACACAGCAAACACC[-/TA]TGTCATTGCTTTGTG	127544
rs566935958	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964911	ACAACCCTTGCGCCC[C/G]GGTCTAGGAGTGCGC	127544
rs566959053	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32938809	CTCTCCAGTAGCCCT[G/T]AAGTCCAAGTCAAAC	127544
rs567006989	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32958173	TAAGCCTTAAAGATG[C/T]TACAGAAAAAACAAA	127544
rs567065551	snp	A/G/T	0.00438332	0.0466095	intron-variant	RNF19B	GRCh38.p7	1:32942957	CATCCTGGCTAACAC[A/G/T]GTGAAACCCCATCTC	127544
rs567078542	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964956	CGGGGTGGGGCCGAG[A/C]GAGCTGGGGCGGAGC	127544
rs567256777	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32960180	CTATCCTACAAATAT[C/T]CTGTAAACAAATCAT	127544
rs567293498	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32948638	GCAAGGAGATTTCCT[C/T]AGGGAGAAAGATGTT	127544
rs567601139	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32942005	AGTAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC	127544
rs567606795	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32947265	TTGTGTTTCATTTAC[A/G]CAATGAATGTTTGTT	127544
rs567615775	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32959370	CACCCGTCAGTCTCC[C/T]AGAGATTCTGAAAGG	127544
rs567740936	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32963403	GCCAAATATCCCCTC[C/T]CCACTCTCATTAAGA	127544
rs567756247	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933502	CCTTGTGAGCCGCCC[A/G]CCTCAGCCTCCCAAA	127544
rs567791510	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32961449	CACTTACTAGTTATA[A/T]GACCCTGAACAAGTC	127544
rs567807882	snp	A/G	0.00279162	0.0372561	intron-variant	RNF19B	GRCh38.p7	1:32952601	CAAAAAATTAGCTGG[A/G]CATGGTGGCGGGCGC	127544
rs567870995	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32958855	TAGGCAGGGGAGTGA[C/T]ACAGATGTTCTCCTT	127544
rs567885246	snp	C/T	0.00438332	0.0466095	intron-variant	RNF19B	GRCh38.p7	1:32941278	GGCTGGGTGTGGTGG[C/T]TCATGCTTGTAATCC	127544
rs567936128	in-del	-/AGTA	0.00114262	0.0238747	intron-variant	RNF19B	GRCh38.p7	1:32949789	ACTAGGTAAGGAAAC[-/AGTA]AGAGATACCAGTAAG	127544
rs568054011	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965070	TCCGCCTCCAATTCC[A/G]TCACCATGACACCCA	127544
rs568111713	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32951336	CGCCCCTTTGCAGAT[A/G]CAGCCCTGGGCACAC	127544
rs568128583	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963856	GCTTAGCAGCCACCT[A/C]GAGCCCTGGGGCAGG	127544
rs568232070	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32953764	AAGTTACTGGATGAC[A/C]TCAGAAAAGCACTAA	127544
rs568234965	snp	A/G	0.000399281	0.0141238	synonymous-codon	RNF19B	GRCh38.p7	1:32945590	AGCCAAATTCCTCTT[A/G]TGTTTGGAGGTTTTC	127544
rs568341204	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	RNF19B	GRCh38.p7	1:32932025	TGGAACCAAATACTA[A/T]ATTAGCCAGGATTCA	127544
rs568350613	in-del	-/T			intron-variant	RNF19B	GRCh38.p7	1:32944694	ATTACTGCACCTTTC[-/T]TTTTTTTTTTTTGAG	127544
rs568404139	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32957551	TGAAAGTATCTGTTG[A/G]AGCCAGGTGTGGTGG	127544
rs568425382	snp	A/G	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32950933	CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT	127544
rs568442359	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963229	ACACATAGTGCTCAG[A/G]GTACCCGAGAGCCTA	127544
rs568552269	snp	A/G	0.00398564	0.0444627	intron-variant	RNF19B	GRCh38.p7	1:32944890	AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	127544
rs568590566	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951234	AGTGTTGTATTTTTT[A/T]AAAAATCCAGGTTTG	127544
rs568717445	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967169	TTGGCAACACCAAAG[A/G]GTCCTAAAGGAGGGG	127544
rs568825644	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32958971	TTGGGGAATGCAGGG[A/G]AAAGTTGTGGAACAG	127544
rs568855071	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966397	GATCGCGCCGCTGCA[C/T]TCCATCCTGGGCGAC	127544
rs569000160	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32961463	ATGACCCTGAACAAG[C/T]CATTCAATTTCCTTA	127544
rs569016277	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959521	ATTAGCAATGAAACA[C/T]TAGGCCCCATGTTTA	127544
rs569044823	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32939616	ACCTCCAGGGAATGA[G/T]ACTGAAGGACATACA	127544
rs569065477	snp	A/G	0.000118224	0.00768753	missense	RNF19B	GRCh38.p7	1:32964111	AGGTAGCGGCGCAGC[A/G]TGAACTCCTCGTACT	127544
rs569090250	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967170	TGGCAACACCAAAGA[A/G]TCCTAAAGGAGGGGG	127544
rs569124208	snp	C/T	0.00597247	0.0543191	intron-variant	RNF19B	GRCh38.p7	1:32944967	CACTGGAATTACAGG[C/T]GTGAGCCACTGCGCC	127544
rs569189903	snp	A/T	0.00279162	0.0372561	intron-variant	RNF19B	GRCh38.p7	1:32951923	CCTCAGCCTCCCGAG[A/T]AGCTGGGATTACAGG	127544
rs569254358	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32939699	CAGAGCCCATAACTA[C/T]TGCCTTTCTTGGCTC	127544
rs569280795	snp	C/G/T	1.80739e-05	0.0030061	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32936805	GAGCATTCATTCCAC[C/G/T]TCATACTCTGGCTTC	127544
rs569358504	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32938711	AATATCTATTGAAAT[C/T]GTCCCCTCCTTTCTA	127544
rs569379543	snp	C/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32945808	AGATATAAAGTAATA[C/G]AGGCAAAGTTAATCC	127544
rs569429787	snp	C/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32951289	GGAGCAGAGCTGTCC[C/T]CACGTCAGGCATAGC	127544
rs569598638	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32936001	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	127544
rs569616531	in-del	-/AAC			intron-variant	RNF19B	GRCh38.p7	1:32956381	ACTCTCTCTTCAAAT[-/AAC]AACAACAACAACAAA	127544
rs569660893	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32943603	CCTGGGTGACAGAGA[C/T]TCCGTCTCAAAAAAA	127544
rs569915572	snp	A/G/T	0.000346283	0.0131539	missense, synonymous-codon	RNF19B	GRCh38.p7	1:32944068	TTTCACTCCTTTTCC[A/G/T]TTGGCTGTGCTAACT	127544
rs570059554	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32961708	AAAAAAATAAAATCT[A/G]GAGGATACTAACATA	127544
rs570190565	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32944503	TGCTAACCCAATCAA[A/G]AGCCAATCAAGAATC	127544
rs570192908	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32962392	TCCATGAACCTAAAA[A/G]GTCCTTCCTGATACT	127544
rs570298387	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32954284	TTGAGTGTGTAATTT[C/G]GTGCCAAGGAAGTAA	127544
rs570370494	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32935104	CAAAGTGCTGGGATT[A/G]CAGGTGTGAACCACT	127544
rs570375559	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32953474	AATCATAGCAACTCA[A/G]GTTCTCAGGTTTATC	127544
rs570442497	snp	G/T	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32952212	AAACAATCCAATATA[G/T]TTATATAACTATTAG	127544
rs570461932	snp	C/T	0.00279162	0.0372561	intron-variant	RNF19B	GRCh38.p7	1:32956269	CTACTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	127544
rs570490039	snp	C/T	0.000115134	0.00758643	missense	RNF19B	GRCh38.p7	1:32964180	TCGTGCGGGTTGAGT[C/T]GCTCGCTGCACTCGG	127544
rs570530461	in-del	-/GGTT	0.0111196	0.0737302	intron-variant	RNF19B	GRCh38.p7	1:32953986	GCTCTCGGCTTACTG[-/GGTT]CAACCTCTGCCTCCT	127544
rs570718096	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32937552	CCCTGTTTCTAAAAT[A/T]AAAAAAATTAGCTGG	127544
rs570729651	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32944835	CTGGGACTACAGGCA[A/C]CCGCTACCACACCCG	127544
rs570812573	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955922	GAAAGGTGTAGAAAA[A/T]TACATGCTGTGAAGA	127544
rs570997987	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32956399	CAACAACAACAAAAA[C/T]TAGCCGAGTGTGGTG	127544
rs571122125	snp	A/C	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32949329	AGACATATTACTAAG[A/C]AAGTAGGAACTACAT	127544
rs571125170	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32960303	CCCTACCAAATGCAC[A/G]TACAAACAAGGCAGA	127544
rs571187929	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955036	CCTCTCTAGGCAGCT[C/G/T]GTTGCCTACTTCGTG	127544
rs571249099	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954520	GAGGCAGGTGGATCA[C/T]CTGAGGTCAGGAGTT	127544
rs571263110	snp	C/T	0.0103295	0.0711199	intron-variant	RNF19B	GRCh38.p7	1:32939864	CAGCAAGTCAGTCTC[C/T]AATTATGTCTGTCTG	127544
rs571487933	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32958432	CAAAAGATGGTTGGA[C/G]ATGGCCGGGCGTGGT	127544
rs571563818	in-del	-/TC			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965222	TCACCTTCCAACATT[-/TC]TGTTTATTAAGCAGA	127544
rs571574474	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32934606	GAATCACTTGAACCC[A/G]GGAGGCTGAGGTTGC	127544
rs571614107	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32935345	GGTTTCACCATGTTG[C/G]CCAGGCTGGTCTCGA	127544
rs571869228	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32948822	GATTTGCTGTTAACA[C/T]AGCCCACAATCCCTT	127544
rs571935009	snp	A/G	4.94466e-05	0.00497201	synonymous-codon	RNF19B	GRCh38.p7	1:32948338	GATAATGTATGCACT[A/G]CATCGTGGGCATGGC	127544
rs571993702	in-del	-/CTGTAGTCCCAGCTACTCAGGAGG	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32958591	CATGGTTGCAGGTGC[-/CTGTAGTCCCAGCTACTCAGGAGG]CTGAGGCAGGAGAAT	127544
rs572050552	in-del	-/TGCAGGAGCCGGCGCACA	0.00398564	0.0444627	intron-variant	RNF19B	GRCh38.p7	1:32951421	TGCACTCTTTGCACT[-/TGCAGGAGCCGGCGCACA]TGCAGGAGCCGGCGC	127544
rs572229662	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954591	TAAAAATACAAAAAT[C/T]AGCCAGGCATGGTGG	127544
rs572230078	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32935025	TTAGTAGAGACGGGG[A/T]TTCACCATGTTGGCC	127544
rs572282158	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32954669	CTTGAAACTGGGAGG[C/T]GGAGGTTGCAGTGAG	127544
rs572320773	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32957424	ATTTTCTATCTATCT[A/G]TGTATCAATTATCTG	127544
rs572347937	snp	A/G	0.00358779	0.0422022	intron-variant	RNF19B	GRCh38.p7	1:32960596	AGCCATGATCATGCC[A/G]CTGCACTCCAGCCTG	127544
rs572414078	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959945	GGTCCCAGCTACTCA[A/G]GAGGCTGAGGCAGGA	127544
rs572485217	snp	C/T	0.00159617	0.0282053	intron-variant	RNF19B	GRCh38.p7	1:32952695	TGCAGTGAGCAGAGA[C/T]TGCGCCACCATGGGT	127544
rs572538910	in-del	-/A			utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32936734	TCTCTACCCCTTGGA[-/A]AAAAAAAAAAAAAAA	127544
rs572681471	snp	A/G			missense	RNF19B	GRCh38.p7	1:32942327	GCTGCAAAGCTGGCC[A/G]TTTCGCTGTAAGGAC	127544
rs572829281	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940692	CCTCTACCTTCCTAT[C/T]CTGCTTTGTTCTACC	127544
rs572837952	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32946722	AGCAAAGGACAAGGC[C/T]AGACTATTAGAGCTC	127544
rs572879774	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933320	AGTGCAGTGGCGCAA[C/T]CTCAGCTCACTGCAA	127544
rs572899211	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32946164	AATGTGAACCATCAT[A/G]CCTGGCCCAGCATTC	127544
rs572940209	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966616	TCTGTTATTAATAAG[C/G]AATGGTAAGATGGGC	127544
rs572941312	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940218	CTCCTACTTAGGTGG[C/T]TGTCAGATGCTGGTT	127544
rs572993458	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32958496	CTGAGATGGGTGGAT[C/G]ACGAGGTCAGGAGAT	127544
rs572995621	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965643	TTCAATTGCAAATAA[C/G]AAAAGAAAAAAATAG	127544
rs573014669	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32947434	GGAGGCCGAGGCAGG[C/T]GGACCACCTGAGGTT	127544
rs573092000	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959094	GCTTGCTTGATCTTC[C/T]CTCATAAATGTGCTA	127544
rs573115002	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951054	ATGTTGGCCAGGATG[A/G]TCTCGATCTCTTGAC	127544
rs573115107	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32957758	AGAATCGCTTGAACC[C/T]GAGAGGCAGAGGTTG	127544
rs573118776	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32938942	GCCAGGAAGCTCTCT[C/G]TCCAGTTCTATCACT	127544
rs573212154	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32952326	TAGCCAGGTGAGATG[C/G]CTCATGCCTGTAATC	127544
rs573219504	snp	C/T			downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32935975	GTGGGTCTCAAACAG[C/T]TGGCCTCAAATGATC	127544
rs573221272	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964772	CGCCCGGCCGCCGCC[G/T]ACGCCGCCACCACCG	127544
rs573308632	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32944627	CTGTTAAGAGAACAG[A/G]ATCTGAAGGCAGATT	127544
rs573459145	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32937950	GAAGAAGCCAGAATA[C/T]CTACTAGTGGGAGTA	127544
rs573496168	snp	C/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32959658	AGAACTATAAAAAAT[C/G]AGTTATTTGTATTTT	127544
rs573506746	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959196	TTTCCTGGGATCAGG[C/T]GGGAGGAAGGATTCT	127544
rs573637618	snp	A/C	0	0	intron-variant	RNF19B	GRCh38.p7	1:32940829	GACCAAGCAAGTCAC[A/C]ATCTTTTTAGTTACA	127544
rs573679531	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965706	GAGACGGTTTTGCTC[C/T]GTCACCCAGGTTGGA	127544
rs573765701	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966796	TGTGCCTGTAGTCCC[C/T]GCTACTTGGGAGACT	127544
rs573767465	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32934453	TAGGAGGCTGAGGTG[A/G]GGGGAATCACTTGAG	127544
rs573825072	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32941569	AAATAAATAAGCCAT[A/G]ATACAGCATAAATGC	127544
rs573829020	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933886	CCCAAATCTCACAGC[G/T]GTAGTAAGTGGAACC	127544
rs573852974	snp	A/G	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32938157	AAAAAAAAAAAAAAA[A/G]AAAGAAAAAATACAT	127544
rs573884658	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32953218	TCTTCAAGCAACCCT[C/G]CCGCCTTAGCCTCCC	127544
rs573914951	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32945256	AAACTAGGGCTTAAA[A/G]TAAGTTTCTGTAATT	127544
rs574003147	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32957215	TCTTGCTATTACCCA[C/G]GCTGGTCTCGAACTC	127544
rs574018310	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32946930	CACACTGCACCCTGC[A/T]CTAATGAACACTCTG	127544
rs574038978	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32939101	CTTATACTCAGTCCT[C/T]AACAACAAAGGAACT	127544
rs574042007	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32932669	CTTTTTGAAAGCTGG[C/T]CGCAAGCACTGCATC	127544
rs574098882	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32934747	ACTCATACAAAGTAA[C/G]TCACTCTAAGATTTG	127544
rs574357443	snp	A/T	0.00199481	0.0315187	intron-variant	RNF19B	GRCh38.p7	1:32957170	GTCCACGTTTTCAGG[A/T]TGATCTCTAGTCATT	127544
rs574369259	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32957795	GCTGAGATGGCACAA[C/T]TGCACTCCAGCCTGG	127544
rs574489197	snp	G/T	0.000399281	0.0141238	missense	RNF19B	GRCh38.p7	1:32964372	CCGCCCTCCGCCGCC[G/T]CCTCATCGTCGAACC	127544
rs574601356	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32953354	TCTATTCCAATACTC[C/T]CCCGCAATATTCAAA	127544
rs574751954	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963523	GAGTTCGAGACCAGC[C/T]TAGCCAACATGGTGA	127544
rs574862590	snp	C/T	0.000115303	0.00759199	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937120	CCTCTTCACTGCCTC[C/T]GCCACCACTACCTTC	127544
rs574931075	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955383	TATAAACCCACTTTA[C/G]TGGTAAACCCCTAAG	127544
rs574937331	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32961826	TGCATTTTTATTGAT[A/G]TGAGCAAAGACAGAA	127544
rs574966520	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32962648	ACCTTGATATATAGG[A/C]TACAATTAAAAGTCC	127544
rs574973825	snp	C/T	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32939290	CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA	127544
rs575036338	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32944250	ATGGACAAACCACTT[C/T]ATAAAGAAAGGAAGA	127544
rs575111942	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32955976	GGCTCATGCCCATAA[A/C]CCCAGAACTTTGTCA	127544
rs575118099	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32943633	AAAAAAAGAAATTCC[C/T]ATTTAAATGGGGATA	127544
rs575130494	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32952262	ATATGTCAATTAAGC[A/G]CTCAGATTACTCTAA	127544
rs575148462	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32951495	TTCGAGCAAAGGAGA[C/T]GCTGGAGCTCCCACC	127544
rs575228058	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32946620	ATACAGCTAGTATTA[C/T]CATAGGGCTTGATAA	127544
rs575305374	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32948179	TCCCTAAATCAGTAA[C/G]AGAATGAGACTACGA	127544
rs575311426	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32954883	ATGGCGTAAAAACAT[C/G]GTACACTCTGTCCTA	127544
rs575327953	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32958266	TTAGCATATTAGCAT[C/G]TTTAAAGATTTAAGA	127544
rs575341280	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32946107	CTGGGCTCAACTGAT[A/C]TACCTGCCTTGGCTT	127544
rs575388555	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32956662	TACAACTTTTACTCA[C/T]TTTATTAATTTCCTA	127544
rs575451252	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32956103	GGGCATGGTGGCTCA[A/T]GCCTGTAATCCCAGC	127544
rs575506164	snp	C/T	0.000575429	0.0169524	synonymous-codon	RNF19B	GRCh38.p7	1:32964641	GGGTGCGGCCGCATG[C/T]AGCGATGTGGAGCGC	127544
rs575638890	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32957885	TCTATACTATTCTTG[C/T]TTATCTCTTTCATCT	127544
rs575790576	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32943136	ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA	127544
rs575873955	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32944383	GTATAACCTTGGACC[C/T]ATCTTCCCAGGGTTG	127544
rs575931080	in-del	-/A	0.00159617	0.0282053	intron-variant	RNF19B	GRCh38.p7	1:32953939	TTGAGACGGAGTTTC[-/A]CTCTTGTTGCCCAGG	127544
rs575936211	snp	A/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32950999	CATGCATCACCATGC[A/G]CAGCTAATTTTTGTA	127544
rs575941827	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF19B	GRCh38.p7	1:32941891	CACGAGGTCAGGAGA[-/T]TTGAGACCATCCTAG	127544
rs576204796	snp	C/T	6.58903e-05	0.00573941	missense	RNF19B	GRCh38.p7	1:32949605	AACTGAGACCTGAAG[C/T]GTGTTTGGTCCGAAC	127544
rs576293610	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32955321	TGTATCCATGTATCT[A/G]TTGGCTTATTATATG	127544
rs576354071	snp	A/C	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954746	TCCATCTCAAAAAAA[A/C]AAAAAAACAATCTCC	127544
rs576401708	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32954161	AAGTGATCCTCCTGC[C/T]TCAGCCTCCCAAAGT	127544
rs576524367	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32961158	TAAACATTAATTAAA[C/T]CTCTCAAGTCAGGAA	127544
rs576528478	snp	C/G	0.000489135	0.015631	intron-variant	RNF19B	GRCh38.p7	1:32937344	ATGGGTTCAGGATTA[C/G]GAATTTCAAAAAGAT	127544
rs576566052	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32941275	ATGGGCTGGGTGTGG[C/T]GGTTCATGCTTGTAA	127544
rs576632879	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32952603	AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCGCCT	127544
rs576772818	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32963424	CTCATTAAGAGATAC[A/T]CCCCACCTTGGCCGG	127544
rs576838816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32960749	CAGCAATAATCCCAG[C/T]ACTTTGGGAGGCCAA	127544
rs577243298	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32935565	TCCTTTCATTACAAA[C/T]CTCAGATTTTAGTCC	127544
rs577304736	snp	A/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32943286	TCAGCTCTGTGAAGC[A/T]CTTAATAGATAGTAA	127544
rs577324872	snp	A/G	0.000798403	0.0199641	intron-variant	RNF19B	GRCh38.p7	1:32949120	ATTCCTCCTTTTAAG[A/G]TTAATCATTAATCTA	127544
rs577603943	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32959393	CTGAAAGGGTTTTAA[C/G]ATTAGCAACAGGATA	127544
rs577607485	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32955599	AAATTAGCTAGGCGT[A/G]GTGGTGCATGCCTGT	127544
rs577654377	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32949947	TTGACCAACTGTAAA[A/G]TATATCCCATGTGAG	127544
rs577669502	in-del	-/TAAC			intron-variant	RNF19B	GRCh38.p7	1:32955090	ACTTACATTATAATG[-/TAAC]TAACTGTTTATATGC	127544
rs577718215	snp	C/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32947504	CCTCCACTAAAAATA[C/T]AAAAATTAGCTGGGC	127544
rs577757892	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32956927	CTTGTCACAATGAAC[G/T]GTACCCTTAACATCT	127544
rs577787877	in-del	-/TTCCC			intron-variant	RNF19B	GRCh38.p7	1:32960096	TCCCACTGAAATTGG[-/TTCCC]TTATTTATGAATAAA	127544
rs577806774	in-del	-/TTA	0.00597247	0.0543191	intron-variant	RNF19B	GRCh38.p7	1:32939481	GCAGGCCCTGCCTAC[-/TTA]TTATTATGCATCTCT	127544
rs577814526	snp	G/T	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32934989	GGTGTGCGCCACCAC[G/T]CCCAGCTAATTTTTG	127544
rs577901249	snp	C/T	0.00557542	0.0525036	intron-variant	RNF19B	GRCh38.p7	1:32948031	CCAGACTACCTGTAA[C/T]ATGGCAAGCAAAGAA	127544
rs577978204	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966860	AGACTGCAGTGAGCC[A/G]TGATTATGCCACTGC	127544
rs578085453	snp	C/G	0.000399281	0.0141238	intron-variant	RNF19B	GRCh38.p7	1:32940004	GTCAGTAGCAGCCTG[C/G]AGCTGCACATTCAAG	127544
rs745334395	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32958664	GAGCTTGCAGTGAGC[C/T]GAGATTGCACCACTG	127544
rs745335745	in-del	-/AAAAAAGAAAATCCAGGTCAGCAGGTTAGGACATCAATCTTTTGCCAGAG	1.78503e-05	0.00298744	intron-variant	RNF19B	GRCh38.p7	1:32945638	GTGAATCTAAGAATA[lengthTooLong]AAAAAAAGGACAGGT	127544
rs745352504	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32956852	AGTCATGTAACATAA[C/G]TAGGCTACCCATTTA	127544
rs745419943	snp	C/T	3.29522e-05	0.00405894	missense	RNF19B	GRCh38.p7	1:32945585	GTGATAGCCAAATTC[C/T]TCTTGTGTTTGGAGG	127544
rs745438289	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32943237	TACGAGTAGAAACCA[C/T]ATTAAAGTAAAAGTC	127544
rs745481092	in-del	-/G			intron-variant	RNF19B	GRCh38.p7	1:32950708	ACTTGGCTAATTTTT[-/G]GTAATTTGCATAGAG	127544
rs745670973	snp	A/G			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966733	TTGAGCAACATGGCA[A/G]AACCCCATCTCTACA	127544
rs745715638	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32934594	TCTGAGACTTGAGAA[A/T]CACTTGAACCCGGGA	127544
rs745770373	snp	G/T	1.64933e-05	0.00287165	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937215	AGCTGATAGTGGCTT[G/T]GTTTGGCTTCAATGT	127544
rs746016954	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32950386	TCATAGCTGAAGCTG[C/T]TTTAGGAGTAGTTTG	127544
rs746030763	snp	C/G	1.74989e-05	0.00295789	intron-variant	RNF19B	GRCh38.p7	1:32942207	CTCAATGTGTTACTT[C/G]TTATAATTCTAACCA	127544
rs746038024	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32955298	CTGCTCTAAAGCAAT[C/T]TTTTCAATGTATCCA	127544
rs746066588	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32952469	AAAAAACAGCCTGGC[A/G]TGGTGGCTCACACCT	127544
rs746169988	in-del	-/A			intron-variant	RNF19B	GRCh38.p7	1:32958719	AGCGAGACTCCATCT[-/A]AAAAAAAAAAAAAGA	127544
rs746194827	in-del	-/TTTCT			intron-variant	RNF19B	GRCh38.p7	1:32938993	AGTCACTCTGAATTC[-/TTTCT]TTCTTTAAATACCTA	127544
rs746266218	snp	A/C	1.64746e-05	0.00287002	missense	RNF19B	GRCh38.p7	1:32949715	AACTCAGTCTGGCAA[A/C]CTTCCCTCTCACAAG	127544
rs746284383	snp	C/T			downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32936322	AGATGACTACTGCGG[C/T]TGGATTTGAATACAA	127544
rs746333968	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32962115	CTGGGACTACAGGTG[C/T]GCACCACCATGCCCG	127544
rs746338555	snp	C/T	3.30442e-05	0.0040646	intron-variant	RNF19B	GRCh38.p7	1:32948212	GGAATGGATGCATTT[C/T]CCATCTTACCTGAGG	127544
rs746417554	snp	C/G			utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936816	CCACTTCATACTCTG[C/G]CTTCTCCACCTTCTG	127544
rs746450167	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32953434	TCTACAGTTTGCTTG[C/T]TTATTTGAATGTACA	127544
rs746474667	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32959124	AGGGATGAAAAAAGC[C/T]TCCTGTTTATGGGAT	127544
rs746475896	in-del	-/CA			intron-variant	RNF19B	GRCh38.p7	1:32955748	AGCTAAACCCTGTCT[-/CA]AAAAAAAAAAAAAAA	127544
rs746529101	in-del	-/TCTGAGAACTATGCTGCTCATA			intron-variant	RNF19B	GRCh38.p7	1:32957911	CATCTCTATTCTTCC[-/TCTGAGAACTATGCTGCTCATA]TTTCTTATCTTTTTC	127544
rs746577302	snp	C/T	1.64735e-05	0.00286993	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937038	TCAGGCTGGGCCAGG[C/T]TGATGTCCCAAGGTT	127544
rs746583286	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933915	CCCAGATAAGAAATA[C/T]AGGTTTAGCCATAAA	127544
rs746628622	snp	C/T	1.65263e-05	0.00287452	synonymous-codon	RNF19B	GRCh38.p7	1:32945611	GGAGGTTTTCCTTCC[C/T]TCATACCTGCTGTGA	127544
rs746650142	snp	C/T	1.6473e-05	0.00286988	intron-variant	RNF19B	GRCh38.p7	1:32946390	GCACAGAAACCAGCA[C/T]GTCTTTCTTACCTTC	127544
rs746665097	snp	A/C	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936966	CACTCATCTGAGGTG[A/C]TGTCTGGCACATCGT	127544
rs746931118	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32955870	TCTGCTCTTTTAGCT[C/T]AACCAATCAGTCAGG	127544
rs747090062	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32963348	GTGGACACACCCCTC[C/T]GACGCGCTGCCCCCT	127544
rs747090109	snp	C/G/T	1.64732e-05	0.0028699	missense	RNF19B	GRCh38.p7	1:32949593	ATTCTTGCCCATAAC[C/G/T]GAGACCTGAAGTGTG	127544
rs747194979	snp	A/C	1.69994e-05	0.00291538	intron-variant	RNF19B	GRCh38.p7	1:32942474	ACTGGGGATAGAACC[A/C]AACATCCAATTCAAG	127544
rs747250374	in-del	-/A	1.6522e-05	0.00287414	intron-variant	RNF19B	GRCh38.p7	1:32938348	TTCTGAAGACCTAGT[-/A]CCCAACGAAAAAATG	127544
rs747270919	snp	A/T	1.82557e-05	0.00302118	utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32936756	AAAAAAAAAATTCCA[A/T]AAGATGCAGTTACAA	127544
rs747302267	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32938006	CCAGTTTCTCAAAAT[A/G]AAAGAGAAAGAAGCT	127544
rs747312264	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32959968	AGGCAGGAGAATGGC[A/G]TGAACCCGGCAGGCA	127544
rs747426073	snp	C/T	1.64743e-05	0.00287	synonymous-codon	RNF19B	GRCh38.p7	1:32942344	TTCGCTGTAAGGACC[C/T]TGCATAACACTAAGT	127544
rs747458911	snp	C/T	0.000263635	0.0114782	missense	RNF19B	GRCh38.p7	1:32949731	CTTCCCTCTCACAAG[C/T]TAGCTTCGGGCAGCT	127544
rs747655930	snp	C/G	0.000115334	0.00759299	missense	RNF19B	GRCh38.p7	1:32964130	ACTCCTCGTACTTGT[C/G]CATAAGCGGCGGGTC	127544
rs747659175	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32934882	CTGTCACCCAGGCTG[A/G]AGTGCAAAGGCGCGA	127544
rs747674056	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32935132	ACTGCGCCCAGCCCA[C/T]TATTTTATTTTTTAT	127544
rs747720744	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965155	TGATGGTTCAGTTAC[A/G]TTATTTATAAAAAGC	127544
rs747769624	snp	A/G	1.6473e-05	0.00286988	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32937184	GAGCGAGTCCTCCGT[A/G]CTGCTTCCACTCACC	127544
rs747793270	snp	C/T	1.6473e-05	0.00286988	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32937085	TTTCTGTTCACAGCT[C/T]TGGTGTCTGCAGGGG	127544
rs747909326	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32955391	CACTTTAGTGGTAAA[A/C]CCCTAAGTTCTGAAT	127544
rs747973231	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32953357	ATTCCAATACTCTCC[C/T]GCAATATTCAAAGAC	127544
rs747984301	snp	A/G	1.65693e-05	0.00287826	synonymous-codon	RNF19B	GRCh38.p7	1:32946414	TACCTTCCTTCCAAC[A/G]TAAACAGGAATGCCA	127544
rs747995305	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32954606	TAGCCAGGCATGGTG[C/G]CGCATGCCTGTAATC	127544
rs748156725	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32951040	GATAGGGTTTCACCA[C/T]GTTGGCCAGGATGGT	127544
rs748238841	snp	C/T	1.65034e-05	0.00287253	missense	RNF19B	GRCh38.p7	1:32948361	GGCATGGCTTGATGT[C/T]ATCTGCTATGAGTGG	127544
rs748254569	snp	A/C			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933543	TACAGGCATGAGCCA[A/C]CACGCCCGGCCAAGC	127544
rs748283887	snp	A/C	1.64751e-05	0.00287007	synonymous-codon	RNF19B	GRCh38.p7	1:32949585	TGGTCCAGATTCTTG[A/C]CCATAACTGAGACCT	127544
rs748308497	snp	A/G/T	0.000153137	0.00874919	intron-variant	RNF19B	GRCh38.p7	1:32938320	CATACAGCCCTAACA[A/G/T]GAGGCATTGAACTTC	127544
rs748327551	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32952524	GAGGCAGGCAAGTCA[C/G]AAGGTCAGGAGTTCG	127544
rs748338174	snp	C/T	1.6922e-05	0.00290873	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936872	TAGGGCAGAGAGGTT[C/T]ATATGGGCACTTGGG	127544
rs748514087	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32959326	ATCTGCCCCTGTACA[A/C]CAGGAAATTTTCTGT	127544
rs748533059	in-del	-/AGA			intron-variant	RNF19B	GRCh38.p7	1:32948097	TTAGAGGAGCATGTC[-/AGA]AGAAGTTTTCACAGC	127544
rs748568922	snp	G/T	1.8176e-05	0.00301458	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32936784	CAAGTGTGCTTCTCA[G/T]AACAGGAGCATTCAT	127544
rs748575540	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32943004	AATTTAGCCGGGCGT[C/G]GTGGCGGGTGCCTGT	127544
rs748592065	in-del	-/TATT	0.000119304	0.00772256	intron-variant	RNF19B	GRCh38.p7	1:32942241	CTGTCAGAAATTATC[-/TATT]TGTTTACCTGCTATA	127544
rs748607981	snp	A/G	0.000230745	0.0107387	synonymous-codon	RNF19B	GRCh38.p7	1:32942400	TCAATACACTAGTCA[A/G]GCCTTCAATGCTGCT	127544
rs748636082	snp	A/G	0.000313038	0.0125068	synonymous-codon	RNF19B	GRCh38.p7	1:32964572	GGCCGAGGCAGAGAA[A/G]ACGCTGTGCAAGGTG	127544
rs748691186	snp	C/T	1.75505e-05	0.00296225	intron-variant	RNF19B	GRCh38.p7	1:32942499	TTCAAGACAGCAGAG[C/T]ATCAAAACAGTCAGT	127544
rs748801064	snp	C/T	0.000385728	0.0138822	missense	RNF19B	GRCh38.p7	1:32964654	TGTAGCGATGTGGAG[C/T]GCGGCGACTCGGAGT	127544
rs748967076	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32959075	AATTTGTCTTGCTCA[A/G]AGAGCTTGCTTGATC	127544
rs748971939	snp	A/C			downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32936262	CTACAAAGTCCAAAA[A/C]AAGCCTAGCTTTGCT	127544
rs749044199	in-del	-/C			intron-variant	RNF19B	GRCh38.p7	1:32962063	TGCACCTCTGCCTCA[-/C]CAGGTTCAAGCGATT	127544
rs749134494	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32942078	CTCCAGCCTGAGCCA[C/T]AGAGTGAGACTCTGT	127544
rs749138177	snp	A/G	1.64732e-05	0.0028699	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937200	CTGCTTCCACTCACC[A/G]GCTGATAGTGGCTTG	127544
rs749168066	snp	A/T			downstream-variant-500B	RNF19B	GRCh38.p7	1:32932270	ACTACAAGAAAACAT[A/T]TCGCAAACTGCTATC	127544
rs749189873	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32956427	GTGGGGCGCGGTGGC[A/G]TGTGGTGGCACATGC	127544
rs749208560	in-del	-/G			intron-variant	RNF19B	GRCh38.p7	1:32958579	AAATTAGCCAGGCAT[-/G]GTTGCAGGTGCCTGT	127544
rs749228160	snp	C/T	3.32381e-05	0.00407651	intron-variant	RNF19B	GRCh38.p7	1:32948184	AAATCAGTAAGAGAA[C/T]GAGACTACGAAAGGA	127544
rs749297291	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32939967	GATAAGAGACAACCA[C/G]AGTCATGAGATGCAC	127544
rs749339677	snp	A/G			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966824	ACTGAGGTGGGAGGA[A/G]TGCTTGAGCCTGGGA	127544
rs749359235	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32954344	GCAATCTATTACTAC[C/G]ACACAGAATTACTCA	127544
rs749435826	snp	A/G	3.35362e-05	0.00409475	intron-variant	RNF19B	GRCh38.p7	1:32938568	TTAATATGAGACCTG[A/G]GTATTCCAAGACAGT	127544
rs749528775	snp	A/G	4.94197e-05	0.00497066	synonymous-codon	RNF19B	GRCh38.p7	1:32949696	CTGCTTGCAGTGGTA[A/G]CAGAACTCAGTCTGG	127544
rs749594595	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32961207	GATAAGAAAAATAAC[A/G]TAGGTAGGAGGCTGT	127544
rs749685963	in-del	-/C			intron-variant	RNF19B	GRCh38.p7	1:32941845	ACTCATGCCTGTAAT[-/C]CCAACGGTTTGGGAG	127544
rs749713428	snp	A/C	1.81194e-05	0.00300988	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32936797	CAGAACAGGAGCATT[A/C]ATTCCACTTCATACT	127544
rs749760828	snp	G/T	1.8542e-05	0.00304478	synonymous-codon	RNF19B	GRCh38.p7	1:32944134	AACCCCATAAACATA[G/T]GCCAGCATAATGGGG	127544
rs749811909	snp	C/G	1.66779e-05	0.00288768	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936886	TCATATGGGCACTTG[C/G]GCTCGGTGCACCTTG	127544
rs749995155	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32940139	GCACAGTGTCAGAGA[A/C]CTGGCTTCTAGTTTC	127544
rs750019597	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32949374	GCATTTCAATTTTAT[A/G]TAGTTGGATAACCTA	127544
rs750073347	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32939332	AGCTGGGATTATGGG[A/T]TCCCACCACCACACC	127544
rs750109761	snp	C/T	1.65627e-05	0.00287769	missense	RNF19B	GRCh38.p7	1:32942262	TTTACCTGCTATATT[C/T]TCCCTTGCCACTGGA	127544
rs750143931	in-del	-/G			intron-variant	RNF19B	GRCh38.p7	1:32941149	GATTGCCTGAGTCCA[-/G]GAAGTTGAGGCTGCA	127544
rs750150895	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32960779	AGGCGGGAAAACAGC[G/T]TGAGCCCAGGAGTTC	127544
rs750151747	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32937651	GAGTTCAAGGCTGCA[C/G]TGAGTTATGATTGTG	127544
rs750247261	snp	A/T	0.000329402	0.0128294	missense	RNF19B	GRCh38.p7	1:32949642	AGTCTGGGCCCTCTG[A/T]TGACGGGCCATATCG	127544
rs750301205	snp	A/G/T			intron-variant	RNF19B	GRCh38.p7	1:32947388	AATGAGGCTGGGCGC[A/G/T]GTGGCTCGCGCTTGT	127544
rs750322487	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32958830	AGGTTAGGTAGTCAA[C/T]GAATAGTCTTAGGCA	127544
rs750431385	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32952870	GTGAGCCACGTTTGC[A/G]CCACTGCACTCCAGC	127544
rs750470148	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32956059	ACATGGTGAAATCCC[A/G]TCTCTACGAAAGACA	127544
rs750526811	snp	C/T	1.67789e-05	0.00289641	splice-acceptor-variant	RNF19B	GRCh38.p7	1:32942461	CCAGGCATCTGCCAC[C/T]GGGGATAGAACCAAA	127544
rs750549922	in-del	-/CTT	4.94181e-05	0.00497057	cds-indel	RNF19B	GRCh38.p7	1:32937132	CTCCGCCACCACTAC[-/CTT]CTTCTTCATTCTCTG	127544
rs750559738	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32957590	TGTAATCCCAGCACT[G/T]TGGGAGGGTGAGGCG	127544
rs750651146	snp	A/G	0.000454029	0.0150602	missense	RNF19B	GRCh38.p7	1:32964351	ACCTCCTCCGCGCCC[A/G]GGCCACCGCCCTCCG	127544
rs750792046	snp	A/C/G			intron-variant	RNF19B	GRCh38.p7	1:32963212	CGATAGCGTGGCACA[A/C/G]AACACATAGTGCTCA	127544
rs750864673	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32950623	CTCACTGCAACCTCC[A/G]CATACCAGGCTCAAG	127544
rs750881850	snp	A/C			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965510	TCTTGCCTGGCAGTG[A/C]CTTTGCCTTTCTTTT	127544
rs750888032	snp	C/T	1.64727e-05	0.00286986	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937151	TTCTTCATTCTCTGC[C/T]ATCTGAGCATGAACA	127544
rs750919854	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32954607	AGCCAGGCATGGTGG[C/G]GCATGCCTGTAATCC	127544
rs750922969	snp	A/G	0.000152118	0.00871986	intron-variant	RNF19B	GRCh38.p7	1:32946375	CTAAAGTTGAAACAA[A/G]CACAGAAACCAGCAT	127544
rs750958614	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933034	AAGTAGCACTATCTA[C/T]CACTCTGTCTTCCCT	127544
rs750980955	snp	A/G	8.23621e-05	0.00641672	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937015	TCTCTAGGTCACTGC[A/G]GATGCTTTCAGGCTG	127544
rs751018793	in-del	-/ATTCAGAGC			intron-variant	RNF19B	GRCh38.p7	1:32958066	ATGAGCTCTCAATCT[-/ATTCAGAGC]ATAAGGTTTATGGTT	127544
rs751174624	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32942716	GCCATGGTAGTTACA[G/T]GAAACTATAACTCTG	127544
rs751216536	in-del	-/A			intron-variant	RNF19B	GRCh38.p7	1:32944627	TGTTAAGAGAACAGG[-/A]ATCTGAAGGCAGATT	127544
rs751281176	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32941273	TGATGGGCTGGGTGT[A/G]GTGGTTCATGCTTGT	127544
rs751300605	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32960573	TCAAGGAGTTCAAGG[C/T]TGTAGTAAGCCATGA	127544
rs751366433	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32958293	AAGAAACTCATAAAC[C/T]TGTTTTATTTTGTTT	127544
rs751446250	snp	A/T			downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32935950	GGCGTGGTTTCACCA[A/T]GTTGGCCAGGTGGGT	127544
rs751499392	snp	C/T	1.6473e-05	0.00286988	missense	RNF19B	GRCh38.p7	1:32949656	GTTGACGGGCCATAT[C/T]GCATGTCTGATTTGG	127544
rs751642847	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32945753	ATCCTCTACCCCAAA[C/T]AGGCATCTTTATCAA	127544
rs751655079	snp	A/G	1.72439e-05	0.00293627	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936860	TTGTCCCTCGGCTAG[A/G]GCAGAGAGGTTCATA	127544
rs751690793	snp	A/G			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933109	TGATTGCCTTCCCCC[A/G]TTAAGAGTCTAAGTT	127544
rs751702823	snp	A/G	1.64958e-05	0.00287187	intron-variant	RNF19B	GRCh38.p7	1:32945493	GCTGAGAGAGAAGAG[A/G]TGTGGTCCTGACTAG	127544
rs751748430	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32957801	ATGGCACAACTGCAC[G/T]CCAGCCTGGGCGACA	127544
rs751920254	snp	A/G			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967187	CCTAAAGGAGGGGGA[A/G]AGTTTAATCCTCAAA	127544
rs751940912	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32952308	TTGTATAAAATAACA[C/T]TTTAGCCAGGTGAGA	127544
rs751973019	snp	A/C	0.0570934	0.159019	synonymous-codon	RNF19B	GRCh38.p7	1:32964449	CGGCTCGGCGGGCAG[A/C]GCCTCGGGCGGCGGG	127544
rs751976556	snp	C/G	4.94287e-05	0.00497111	missense	RNF19B	GRCh38.p7	1:32948247	GCAAGTCTGAGATCT[C/G]TTTCATACAAAGCCA	127544
rs752015959	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32939481	GCAGGCCCTGCCTAC[G/T]TATTATTATGCATCT	127544
rs752025494	snp	A/G	0.000101348	0.00711784	intron-variant	RNF19B	GRCh38.p7	1:32937312	GATCATGCTAAACCT[A/G]TTGGTAAAAGCAGTT	127544
rs752030920	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32953797	CAACTTCTAAAGATA[C/T]AAATTAAGTGGACAT	127544
rs752059208	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32934325	CAGGGAAAGGAGGAT[C/T]TCAATTTTTCCTCTG	127544
rs752078296	snp	C/T	1.64727e-05	0.00286986	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32937172	AGCATGAACATGGAG[C/T]GAGTCCTCCGTGCTG	127544
rs752318100	snp	A/G	3.49528e-05	0.00418033	intron-variant	RNF19B	GRCh38.p7	1:32937325	CTGTTGGTAAAAGCA[A/G]TTCATGGGTTCAGGA	127544
rs752357771	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	RNF19B	GRCh38.p7	1:32948281	GAATTCACAGCCACA[C/T]ACTGCACAGGTCATG	127544
rs752568196	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32950095	CTGCCACAGACTCCC[C/T]AGTAGCTGGGATTAC	127544
rs752648459	snp	A/G	3.29603e-05	0.00405944	missense	RNF19B	GRCh38.p7	1:32942297	ATGCCGCCACTCAGC[A/G]TGCCCCCTGAGAGGG	127544
rs752649262	snp	A/G	0.000146081	0.00854514	missense	RNF19B	GRCh38.p7	1:32964273	CGGCACGAGCGGTGC[A/G]GACAGCTGAGGAGGC	127544
rs752703301	snp	G/T	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936996	TCTGACTGTGCATCA[G/T]AACTCTCTAGGTCAC	127544
rs752766906	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32934901	GCAAAGGCGCGATCT[C/T]GGCTCACTGCAACAT	127544
rs752783700	in-del	-/GT			intron-variant	RNF19B	GRCh38.p7	1:32960132	TAAAACCATATTTGA[-/GT]GTAAGAGAAGAAAAA	127544
rs752934272	snp	A/C	1.64803e-05	0.00287052	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936928	TCGAGGGGCAGGCTG[A/C]AGTATGGGAGCGGGG	127544
rs752950770	in-del	-/AAAAAA			intron-variant	RNF19B	GRCh38.p7	1:32952430	AAGACCTTTTCTCTT[-/AAAAAA]AAAAAAAAAAAAAAA	127544
rs753088268	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32954011	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA	127544
rs753120896	snp	A/T	4.95954e-05	0.00497948	intron-variant	RNF19B	GRCh38.p7	1:32938344	GAACTTCTGAAGACC[A/T]AGTACCCAACGAAAA	127544
rs753161582	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32941470	ACTAGAACCCAGGAG[A/G]TGGAGGCTGCAGCGA	127544
rs753166504	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32946825	TCTGCTGAATTCTGT[C/T]TTCCCTAACCCACCA	127544
rs753309172	in-del	-/ACCTGCCT			intron-variant	RNF19B	GRCh38.p7	1:32939175	AAGTACTCCCACAGC[-/ACCTGCCT]ACTTATTTATTATTA	127544
rs753352675	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964819	GGCGATAGAAGCCGA[A/G]CGGCAACGACGAAGT	127544
rs753376612	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32963086	TTTCTCCTATCACAC[C/T]AACCTCTGGGCATTC	127544
rs753396270	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32937670	GTTATGATTGTGTCA[A/C]TGCACTCCAGCCTGG	127544
rs753413006	snp	C/T	1.64936e-05	0.00287168	missense, intron-variant	RNF19B	GRCh38.p7	1:32938512	TTTCCTTTTGGACAT[C/T]GGCTTGAACTTCTAA	127544
rs753502870	snp	C/T	6.60338e-05	0.00574566	intron-variant	RNF19B	GRCh38.p7	1:32938354	AGACCTAGTACCCAA[C/T]GAAAAAATGCAACCT	127544
rs753522948	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32950330	TTTAAAAAGTGGAGG[C/T]GGAGTATCTTATTTA	127544
rs753528968	in-del	-/TC			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965978	ACCTAGCCAGAAATT[-/TC]TCTCTTTCCATGAAA	127544
rs753565983	in-del	-/CAGC			intron-variant	RNF19B	GRCh38.p7	1:32937818	CACACACGTGTATCT[-/CAGC]CAATCTCTTTAAACA	127544
rs753634700	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32944381	CTGTATAACCTTGGA[C/T]CTATCTTCCCAGGGT	127544
rs753653914	in-del	-/C	3.55429e-05	0.00421547	utr-variant-3-prime, frameshift-variant	RNF19B	GRCh38.p7	1:32936841	CTTCTGGCTTCAAGA[-/C]AGTTTGTCCCTCGGC	127544
rs753682305	snp	A/C	1.64765e-05	0.00287019	missense	RNF19B	GRCh38.p7	1:32948326	ATCATTCATCTTGAT[A/C]ATGTATGCACTGCAT	127544
rs753693150	in-del	-/T			intron-variant	RNF19B	GRCh38.p7	1:32963092	TATCACACCAACCTC[-/T]TGGGCATTCTTCTCA	127544
rs753755931	snp	A/G	1.66696e-05	0.00288696	intron-variant	RNF19B	GRCh38.p7	1:32938550	AAAGAGGGGACGTTC[A/G]AGTTAATATGAGACC	127544
rs753786777	snp	A/C	1.64999e-05	0.00287222	missense	RNF19B	GRCh38.p7	1:32944031	TACCTGTGATTGGAC[A/C]ATCATCTTCATCAAA	127544
rs754063635	snp	C/G	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937006	CATCAGAACTCTCTA[C/G]GTCACTGCGGATGCT	127544
rs754233829	snp	A/G/T			intron-variant	RNF19B	GRCh38.p7	1:32941805	CCTATTTGTAAAAGT[A/G/T]AAAAAAAAAAGGCCT	127544
rs754288661	snp	C/G	1.69717e-05	0.002913	intron-variant	RNF19B	GRCh38.p7	1:32946365	ACTAACGAACCTAAA[C/G]TTGAAACAAGCACAG	127544
rs754419951	snp	C/T	3.82922e-05	0.00437546	intron-variant	RNF19B	GRCh38.p7	1:32946597	TGAAGTTAATGTCAA[C/T]ATTACAAATACAGCT	127544
rs754473041	snp	C/T			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964823	ATAGAAGCCGAGCGG[C/T]AACGACGAAGTGATT	127544
rs754723472	snp	A/T	1.6696e-05	0.00288924	intron-variant	RNF19B	GRCh38.p7	1:32946392	ACAGAAACCAGCATG[A/T]CTTTCTTACCTTCCT	127544
rs754792877	snp	A/T			downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32935961	ACCATGTTGGCCAGG[A/T]GGGTCTCAAACAGCT	127544
rs754806686	snp	A/G	0.000131913	0.00812029	synonymous-codon	RNF19B	GRCh38.p7	1:32942287	ACTGGAGAGAATGCC[A/G]CCACTCAGCGTGCCC	127544
rs754894699	snp	C/G	1.70566e-05	0.00292027	intron-variant	RNF19B	GRCh38.p7	1:32949796	AAGGAAACAGTAAGA[C/G]ATACCAGTAAGGTAA	127544
rs754908374	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32935123	GTGTGAACCACTGCG[A/C]CCAGCCCATTATTTT	127544
rs754954642	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32963398	CCTTGGCCAAATATC[C/T]CCTCCCCACTCTCAT	127544
rs755058138	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32934329	GAAAGGAGGATTTCA[A/G]TTTTTCCTCTGGGCC	127544
rs755089134	snp	A/G	1.64849e-05	0.00287092	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936919	CTCTGGGGGTCGAGG[A/G]GCAGGCTGCAGTATG	127544
rs755115178	snp	C/G			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965876	AAATCTCCCTGTGTT[C/G]CTCAGGCTGGTCTCG	127544
rs755123634	snp	C/T	3.29826e-05	0.00406082	missense	RNF19B	GRCh38.p7	1:32944069	TTCACTCCTTTTCCG[C/T]TGGCTGTGCTAACTC	127544
rs755199694	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32944230	TTCTTCTTCCCAGTC[G/T]GGGCATGGACAAACC	127544
rs755324562	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32942997	TACAAAAAATTTAGC[C/T]GGGCGTGGTGGCGGG	127544
rs755392206	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32953989	TCTCGGCTTACTGCA[A/G]CCTCTGCCTCCTGGG	127544
rs755450379	snp	C/T	1.68917e-05	0.00290613	intron-variant	RNF19B	GRCh38.p7	1:32937313	ATCATGCTAAACCTG[C/T]TGGTAAAAGCAGTTC	127544
rs755564304	snp	A/G/T	3.60381e-05	0.00424476	intron-variant	RNF19B	GRCh38.p7	1:32937342	TCATGGGTTCAGGAT[A/G/T]AGGAATTTCAAAAAG	127544
rs755595048	snp	A/G			downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32936126	CTACTAGTGACTATA[A/G]TGCAGAAAAGGGCAA	127544
rs755654553	snp	C/T	1.65184e-05	0.00287384	intron-variant	RNF19B	GRCh38.p7	1:32938349	TCTGAAGACCTAGTA[C/T]CCAACGAAAAAATGC	127544
rs755697335	snp	C/T	1.64741e-05	0.00286998	missense	RNF19B	GRCh38.p7	1:32948283	ATTCACAGCCACACA[C/T]TGCACAGGTCATGTG	127544
rs755724620	snp	A/G	1.64732e-05	0.0028699	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32937193	CTCCGTGCTGCTTCC[A/G]CTCACCAGCTGATAG	127544
rs755816019	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32947768	ACTTACAGTTTAGTA[A/G]GATAAGATAGGTACG	127544
rs755884559	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32957840	CTCCATCTCAAAAAA[A/C]AGTTGTCTGTTGAAT	127544
rs755924704	snp	A/T	1.66324e-05	0.00288374	intron-variant	RNF19B	GRCh38.p7	1:32948172	ATCCTTTTCCCTAAA[A/T]CAGTAAGAGAATGAG	127544
rs755940209	snp	A/C	1.66685e-05	0.00288686	missense	RNF19B	GRCh38.p7	1:32942454	GGGCTCTCCAGGCAT[A/C]TGCCACTGGGGATAG	127544
rs755962377	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32942813	AATATGTTTGGGTCA[C/T]GTGCTGATTTTAATA	127544
rs755988227	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32935120	CAGGTGTGAACCACT[A/G]CGCCCAGCCCATTAT	127544
rs755990537	snp	A/C			utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964777	GGCCGCCGCCGACGC[A/C]GCCACCACCGCCTCA	127544
rs756039953	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32937583	GCATGGAGGCACGTG[C/T]CTGTAGTCCCAGCTA	127544
rs756075990	in-del	-/TG			intron-variant	RNF19B	GRCh38.p7	1:32944724	GACGGAGTCTCACTC[-/TG]TTGCCCAGGCTGGAG	127544
rs756240656	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32952875	CCACGTTTGCGCCAC[G/T]GCACTCCAGCCTGGG	127544
rs756244716	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32954012	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	127544
rs756251436	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32934452	TTAGGAGGCTGAGGT[G/T]GGGGGAATCACTTGA	127544
rs756268186	snp	C/G	1.64773e-05	0.00287026	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936938	GGCTGCAGTATGGGA[C/G]CGGGGGGAGCCACAC	127544
rs756351426	snp	A/G			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966513	TTTTTGCCAAAACAT[A/G]CTCACTCACATGGCC	127544
rs756466037	snp	A/C	1.64746e-05	0.00287002	missense	RNF19B	GRCh38.p7	1:32945550	CTGGGGATGCAATGA[A/C]CGACAAAGTCACTCC	127544
rs756475692	snp	A/G	1.71015e-05	0.00292411	missense	RNF19B	GRCh38.p7	1:32944114	CGACAAAGAGAAATG[A/G]GCACAACCCCATAAA	127544
rs756497357	snp	C/T	6.68572e-05	0.00578136	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936883	GGTTCATATGGGCAC[C/T]TGGGCTCGGTGCACC	127544
rs756503601	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32961172	ACCTCTCAAGTCAGG[A/G]AAGAATTAGACCTAT	127544
rs756621197	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32954627	GCCTGTAATCCAGCT[A/G]CTCGGGAGGCTGAGG	127544
rs756623375	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32954886	GCGTAAAAACATCGT[A/G]CACTCTGTCCTACTT	127544
rs756970603	snp	G/T	1.6477e-05	0.00287024	missense	RNF19B	GRCh38.p7	1:32948328	CATTCATCTTGATAA[G/T]GTATGCACTGCATCG	127544
rs757085052	snp	A/G	1.74653e-05	0.00295505	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936854	GACAGTTTGTCCCTC[A/G]GCTAGGGCAGAGAGG	127544
rs757090377	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933597	ATTTGTGTTCGCCTC[C/T]AGGTGGTGATGATGG	127544
rs757114387	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32944397	CTATCTTCCCAGGGT[C/T]GTCAATAATCAAATG	127544
rs757116499	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32958654	CCGGGAGGTGGAGCT[C/T]GCAGTGAGCCGAGAT	127544
rs757132875	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32946135	CTTCCCAAAGTGCTA[A/G]GCCACGTATTACAAA	127544
rs757388727	snp	G/T	1.6476e-05	0.00287014	synonymous-codon	RNF19B	GRCh38.p7	1:32942314	GCCCCCTGAGAGGGC[G/T]GCAAAGCTGGCCGTT	127544
rs757486387	snp	C/T	3.29473e-05	0.00405864	missense	RNF19B	GRCh38.p7	1:32949704	AGTGGTAGCAGAACT[C/T]AGTCTGGCAACCTTC	127544
rs757526961	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32954397	GTTTTTGGGTACCTG[C/G]TCTGAGCTCTTGCCT	127544
rs757585352	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32949312	AATTGCTCTCCAATC[C/T]GAGACATATTACTAA	127544
rs757597383	snp	A/G	3.29457e-05	0.00405854	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32937010	AGAACTCTCTAGGTC[A/G]CTGCGGATGCTTTCA	127544
rs757665494	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32963089	CTCCTATCACACCAA[A/C]CTCTGGGCATTCTTC	127544
rs757744584	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32942575	TAATGAACAGGTACT[A/G]TGTGCAGTCGCCACA	127544
rs757863865	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32958110	AGGACACTAACCAAA[C/G]GCAGGCCAGCATGGT	127544
rs757875280	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32958844	ATGAATAGTCTTAGG[C/G]AGGGGAGTGATACAG	127544
rs757907579	snp	C/T	1.64754e-05	0.00287009	missense	RNF19B	GRCh38.p7	1:32945577	CTCCTCCAGTGATAG[C/T]CAAATTCCTCTTGTG	127544
rs758007937	snp	A/G	1.68255e-05	0.00290043	intron-variant	RNF19B	GRCh38.p7	1:32946381	TTGAAACAAGCACAG[A/G]AACCAGCATGTCTTT	127544
rs758106831	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32939334	CTGGGATTATGGGTT[C/G]CCACCACCACACCCA	127544
rs758108561	snp	A/T	1.64928e-05	0.00287161	intron-variant	RNF19B	GRCh38.p7	1:32938380	AACCTCTCCTGGACA[A/T]CTGACTGTTCACATA	127544
rs758189473	snp	C/T			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965490	TGGAAGGAGACCCAG[C/T]GTTTTCTTGCCTGGC	127544
rs758339226	snp	A/C	0.000131815	0.00811728	missense	RNF19B	GRCh38.p7	1:32949574	CAACTTATACCTGGT[A/C]CAGATTCTTGCCCAT	127544
rs758420437	in-del	-/CCG	0.0215431	0.101526	cds-indel	RNF19B	GRCh38.p7	1:32964394	CGTCGAACCCAGGCT[-/CCG]CCGCCGCCGCCGCGG	127544
rs758457849	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32946337	AGCTCCTTCCCATTT[A/C]CCTCAAACCTTTACT	127544
rs758463800	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32942739	TAACTCTGATTCCAA[G/T]GCCACTATTCTTTCC	127544
rs758485721	snp	G/T	1.68403e-05	0.0029017	intron-variant	RNF19B	GRCh38.p7	1:32942465	GCATCTGCCACTGGG[G/T]ATAGAACCAAACATC	127544
rs758587378	in-del	-/ATGA	1.64727e-05	0.00286986	utr-variant-3-prime, frameshift-variant	RNF19B	GRCh38.p7	1:32937159	CTCTGCCATCTGAGC[-/ATGA]ATGAACATGGAGCGA	127544
rs758623357	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32950683	CTGGGACTACAGGTG[C/T]GCACCACCACACTTG	127544
rs758664959	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32941957	AAAAAATTAGCTGGG[C/T]GTGGTGGCGGGTGCC	127544
rs758689346	snp	A/G	0.000931098	0.0215565	synonymous-codon	RNF19B	GRCh38.p7	1:32964353	CTCCTCCGCGCCCGG[A/G]CCACCGCCCTCCGCC	127544
rs758711180	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32937885	CAGAGCCCCATGCTA[A/G]CTTACTCAAAATAGA	127544
rs758767669	snp	C/T			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965580	CCTTAGGCTTCCTAG[C/T]GGGAGGCAGGCAAAC	127544
rs758777240	snp	A/G	0.000225708	0.0106209	intron-variant	RNF19B	GRCh38.p7	1:32964023	CGGCTGCAGCCCGCC[A/G]CCACCCGCGCCACGC	127544
rs758842475	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32946935	TGCACCCTGCACTAA[G/T]GAACACTCTGATTTG	127544
rs758909209	snp	A/G	1.6473e-05	0.00286988	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32937019	TAGGTCACTGCGGAT[A/G]CTTTCAGGCTGGGCC	127544
rs758913107	snp	A/G	1.64727e-05	0.00286986	intron-variant	RNF19B	GRCh38.p7	1:32946590	AACAGACTGAAGTTA[A/G]TGTCAACATTACAAA	127544
rs759067640	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32961821	TTCTGTGCATTTTTA[C/T]TGATGTGAGCAAAGA	127544
rs759114944	snp	C/T	1.64751e-05	0.00287007	missense	RNF19B	GRCh38.p7	1:32948253	CTGAGATCTCTTTCA[C/T]ACAAAGCCAACAGAA	127544
rs759215009	snp	C/T	0.000100796	0.00709845	intron-variant	RNF19B	GRCh38.p7	1:32943984	TTATCTTGTATATCA[C/T]AAATTCAAATGGAAA	127544
rs759227697	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32955505	GAAGCCAAGGTGGGT[A/G]GATTGCTTGAGCTCA	127544
rs759227703	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32941287	TGGTGGTTCATGCTT[G/T]TAATCCCAGCACTTT	127544
rs759228193	snp	C/T	3.60334e-05	0.00424446	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936814	TTCCACTTCATACTC[C/T]GGCTTCTCCACCTTC	127544
rs759250973	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32942128	AAAACAAAACAAAAC[A/C]AAACCATTGACAATT	127544
rs759326070	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32944164	GACACCAATACCTGG[C/G]GGAAGAGAAGGAAAC	127544
rs759337268	in-del	-/AAAAAA			intron-variant	RNF19B	GRCh38.p7	1:32952577	AAACGCTGTCTCTAC[-/AAAAAA]TAAAAATACAAAAAA	127544
rs759390897	snp	A/G	0.00024426	0.0110485	synonymous-codon	RNF19B	GRCh38.p7	1:32964239	TATCTCCAGGCGCAG[A/G]TAGTGGCGGAGGCAG	127544
rs759442240	snp	A/G	1.65211e-05	0.00287407	missense	RNF19B	GRCh38.p7	1:32942430	TTTCCCCAATGCTGG[A/G]ATTCTTGAGGGCTCT	127544
rs759511260	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32962740	AGGACTCCCCAGCAT[A/C]TTTTTGTCGCCAAAA	127544
rs759594850	snp	C/T	1.648e-05	0.0028705	missense	RNF19B	GRCh38.p7	1:32945517	TGACTAGCTTACCAA[C/T]ACTAACTGCAGCAAT	127544
rs759649860	snp	C/T	0.000170771	0.00923885	intron-variant	RNF19B	GRCh38.p7	1:32946355	TCAAACCTTTACTAA[C/T]GAACCTAAAGTTGAA	127544
rs759716186	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32957608	GGAGGGTGAGGCGGG[C/T]GGCTCGCTTGAAGTC	127544
rs759729647	in-del	-/CA			intron-variant	RNF19B	GRCh38.p7	1:32939761	CCTTATAATGGGTTT[-/CA]CAGTCAAACCCATCT	127544
rs759842889	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32958448	ATGGCCGGGCGTGGT[A/G]GCTCACGCCTGTAAT	127544
rs759901102	snp	C/G	1.65963e-05	0.0028806	intron-variant	RNF19B	GRCh38.p7	1:32948386	GAGTGGGGGAAGAAT[C/G]GGTAGAAAAAATACC	127544
rs759992619	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32954867	TTGTCCTCAAAGATA[C/T]ATGGCGTAAAAACAT	127544
rs759993810	snp	A/G	8.23676e-05	0.00641693	missense, intron-variant	RNF19B	GRCh38.p7	1:32938463	CTTGCGTTGTCACTA[A/G]TTGCACCAAGACTGG	127544
rs760011322	snp	A/G			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967250	CAACAATTAATGTCT[A/G]TATTTATCTGGCAGA	127544
rs760062496	in-del	-/A			intron-variant	RNF19B	GRCh38.p7	1:32947659	GAGAAACTCTGTCTT[-/A]AAAAAAAAAAAAAAA	127544
rs760165967	in-del	-/GCA			intron-variant	RNF19B	GRCh38.p7	1:32960010	AGCAGAGATGGTGCC[-/GCA]ACTGCACTCCAGCCT	127544
rs760191775	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32950097	GCCACAGACTCCCTA[A/G]TAGCTGGGATTACAG	127544
rs760203644	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32943386	GGAGGCCAAGGTGGG[C/T]GGATCATGGGGTGAG	127544
rs760210076	snp	C/T	1.64727e-05	0.00286986	missense	RNF19B	GRCh38.p7	1:32949620	TGTGTTTGGTCCGAA[C/T]TCGTAAAGTCTGGGC	127544
rs760234261	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32949390	TAGTTGGATAACCTA[C/T]AATGGTCAGAGAGGG	127544
rs760247686	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965141	CCACTTCCAGTAAAT[A/G]ATGGTTCAGTTACAT	127544
rs760380487	in-del	-/ACATT	1.90239e-05	0.00308408	intron-variant	RNF19B	GRCh38.p7	1:32946596	CTGAAGTTAATGTCA[-/ACATT]ACAAATACAGCTAGT	127544
rs760404256	in-del	-/AA			intron-variant	RNF19B	GRCh38.p7	1:32945878	TTTACCTTCTTCTTT[-/AA]TATTTTTTTTTTTGG	127544
rs760505150	snp	C/T	0.000231685	0.0107605	intron-variant	RNF19B	GRCh38.p7	1:32944014	ATAAACATCCTGCTT[C/T]TTACCTGTGATTGGA	127544
rs760591116	snp	C/T	1.76661e-05	0.00297199	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936849	TTCAAGACAGTTTGT[C/T]CCTCGGCTAGGGCAG	127544
rs760659205	snp	G/T	1.66788e-05	0.00288775	missense	RNF19B	GRCh38.p7	1:32946509	TGCCCAGCTGCCAAA[G/T]AATTTTCTTCTTACG	127544
rs760735455	in-del	-/C			intron-variant	RNF19B	GRCh38.p7	1:32955748	AGCTAAACCCTGTCT[-/C]AAAAAAAAAAAAAAA	127544
rs760737343	snp	A/T	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937000	ACTGTGCATCAGAAC[A/T]CTCTAGGTCACTGCG	127544
rs760892264	snp	C/T	1.70174e-05	0.00291692	intron-variant	RNF19B	GRCh38.p7	1:32946359	ACCTTTACTAACGAA[C/T]CTAAAGTTGAAACAA	127544
rs760901640	in-del	-/T			intron-variant	RNF19B	GRCh38.p7	1:32934655	CACTGCACTCCAGTC[-/T]GGGGGACAGAGCCAG	127544
rs760956557	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32959212	GGGAGGAAGGATTCT[A/G]CAGAGGACAGAGGCA	127544
rs760958735	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32957040	TCCATCCAAATTCCA[C/T]TCTGGAAGGTTACTC	127544
rs761016906	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32947242	TCGACAAATTGGCAA[C/T]GAAGGTGTTGTGTTT	127544
rs761023637	snp	G/T	5.12956e-05	0.00506411	intron-variant	RNF19B	GRCh38.p7	1:32942237	ATTTCTGTCAGAAAT[G/T]ATCTATTTGTTTACC	127544
rs761106048	snp	A/G			downstream-variant-500B	RNF19B	GRCh38.p7	1:32932024	TTGGAACCAAATACT[A/G]TATTAGCCAGGATTC	127544
rs761106139	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32942541	TGCAATGACTTTTCA[C/G]AGAACTAATGTATTT	127544
rs761207644	in-del	-/A			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966429	AGCGAGACTCTGTCT[-/A]CAAAAAAAAAAAAAA	127544
rs761223038	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32951859	ATGGAGCGCAGTGGC[A/G]TGATCTCGGCTCACT	127544
rs761303761	snp	A/G	3.31735e-05	0.00407255	intron-variant	RNF19B	GRCh38.p7	1:32938535	ACTTCTAACCTGTGT[A/G]AAGAGGGGACGTTCA	127544
rs761308745	snp	A/C	1.64727e-05	0.00286986	missense	RNF19B	GRCh38.p7	1:32949635	CTCGTAAAGTCTGGG[A/C]CCTCTGTTGACGGGC	127544
rs761320866	snp	G/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933987	GTGAATTGTTCTCTC[G/T]AGGCTTCAAGAGAAT	127544
rs761356642	snp	A/G	3.3232e-05	0.00407614	synonymous-codon	RNF19B	GRCh38.p7	1:32942257	ATTTGTTTACCTGCT[A/G]TATTTTCCCTTGCCA	127544
rs761377578	snp	A/C	0.00231835	0.0339676	missense	RNF19B	GRCh38.p7	1:32949750	CTTCGGGCAGCTGGC[A/C]CAGCCATAGGCAATA	127544
rs761379747	snp	C/T			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967016	ACTGAAAAGCGGGGG[C/T]CAGTGACATAAAAGA	127544
rs761396203	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32953457	AATGTACATGAGATG[C/T]TAATCATAGCAACTC	127544
rs761417176	snp	C/T			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965458	CCTCCTGGTATCTTG[C/T]TTACTTACCAAACTT	127544
rs761460045	in-del	-/AAG			intron-variant	RNF19B	GRCh38.p7	1:32954234	TTTTTTTTCTTGAAA[-/AAG]AAGAACATTGGATAG	127544
rs761560303	snp	A/G	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936973	CTGAGGTGATGTCTG[A/G]CACATCGTCTGACTG	127544
rs761589664	snp	A/T	7.04213e-05	0.00593344	intron-variant	RNF19B	GRCh38.p7	1:32945636	CTGTGAATCTAAGAA[A/T]AAAAAAAGAAAATCC	127544
rs761631934	in-del	-/T	3.29685e-05	0.00405995	intron-variant	RNF19B	GRCh38.p7	1:32949565	GATAATGCCAACTTA[-/T]TACCTGGTCCAGATT	127544
rs761698182	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32940047	TACTGCCTGAGCCTT[C/T]GCTTTGCTGCTCCAG	127544
rs761755779	snp	A/G	3.30376e-05	0.0040642	intron-variant	RNF19B	GRCh38.p7	1:32945467	TCTGGCTAAACTGCT[A/G]TGGTCAGAAAGCTGA	127544
rs761799171	snp	A/G	1.6477e-05	0.00287024	utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32937262	ATTGTTGCATTCTCT[A/G]TGGAGACAAAATCCA	127544
rs761803566	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32940113	GGAAATGAGGGAATG[C/T]AATGGAAAGTGCACA	127544
rs761821734	snp	C/G	0.000221459	0.0105205	missense	RNF19B	GRCh38.p7	1:32964307	GGGCCCGCTCAGGCG[C/G]CAGCCGCACCAGGCA	127544
rs761900387	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32955958	GACACAGCTGGGTGC[A/G]GTGGCTCATGCCCAT	127544
rs762063819	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32963632	CTGAGGCAGGAGAAT[A/C]GCTTGAACCTGAGAG	127544
rs762082993	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32937468	TATAACCCCAGCGCT[C/T]TGGGAGGTCGAGGTG	127544
rs762197597	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32954153	TGGCCTTCAAGTGAT[C/T]CTCCTGCCTCAGCCT	127544
rs762221307	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32943758	GATATAAAGATGTTA[C/T]TATAATCACTACTAC	127544
rs762300816	snp	A/G	1.67826e-05	0.00289673	missense	RNF19B	GRCh38.p7	1:32946524	GAATTTTCTTCTTAC[A/G]GCTCCATGGCTTCTT	127544
rs762344439	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32957258	AATCCTCCCACCTCA[A/G]CCTCCTAAGCAGCTG	127544
rs762355093	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32940182	GAATCACTCTGAGTT[A/G]GAAGAGTCTTTCAGA	127544
rs762453296	snp	C/G	1.64963e-05	0.00287192	missense	RNF19B	GRCh38.p7	1:32942280	CCTTGCCACTGGAGA[C/G]AATGCCGCCACTCAG	127544
rs762515857	snp	G/T	1.64871e-05	0.00287111	missense	RNF19B	GRCh38.p7	1:32942409	TAGTCAGGCCTTCAA[G/T]GCTGCTTTCCCCAAT	127544
rs762525971	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32941119	TCCTAGCTACTCAGG[A/G]GGCTGAGGTGGTAGG	127544
rs762537545	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32954816	CTTGTCACATTCAAA[C/T]GTAGCTAAACACGTT	127544
rs762640962	in-del	-/G			intron-variant	RNF19B	GRCh38.p7	1:32954229	TTTTTTTTTTTTCTT[-/G]GAAAAAGAAGAACAT	127544
rs762881563	snp	G/T	1.64727e-05	0.00286986	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32937100	TTGGTGTCTGCAGGG[G/T]GGATCCTCTTCACTG	127544
rs762956498	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32958340	AGCTTATTTCCTCAC[A/G]AAACATTTTTCTTTC	127544
rs762979044	snp	C/T	3.29755e-05	0.00406038	missense	RNF19B	GRCh38.p7	1:32944042	GGACCATCATCTTCA[C/T]CAAATTCAATTTTCA	127544
rs763076744	snp	A/G			utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32936595	AAAACTAAAAAGAGG[A/G]AGGGGAGGGGAGGGG	127544
rs763188464	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32938676	CAGCGCAAATAGATG[C/T]CCATACATTTTTTCT	127544
rs763210386	snp	C/T	1.64939e-05	0.0028717	missense	RNF19B	GRCh38.p7	1:32948223	ATTTCCCATCTTACC[C/T]GAGGTAATGCAAGTC	127544
rs763215444	snp	A/C	5.41296e-05	0.0052021	intron-variant	RNF19B	GRCh38.p7	1:32938310	GGAGATGGTACATAC[A/C]GCCCTAACATGAGGC	127544
rs763234629	in-del	-/A			intron-variant	RNF19B	GRCh38.p7	1:32963022	CCTACATGGTGCATT[-/A]AAAAGACTGTCATCA	127544
rs763412358	snp	A/G	1.65605e-05	0.0028775	intron-variant	RNF19B	GRCh38.p7	1:32948376	CATCTGCTATGAGTG[A/G]GGGAAGAATGGGTAG	127544
rs763413369	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32945688	AATCTTTTGCCAGAG[A/G]AAAAAAGGACAGGTG	127544
rs763430608	snp	A/G			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967141	GATAAGAACAGAGAT[A/G]TGACCACTGGATTTG	127544
rs763466228	snp	G/T			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965204	TGGTGACTCCCAACT[G/T]GTTCACCTTCCAACA	127544
rs763548417	snp	C/G	1.64727e-05	0.00286986	missense	RNF19B	GRCh38.p7	1:32949628	GTCCGAACTCGTAAA[C/G]TCTGGGCCCTCTGTT	127544
rs763551265	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32939780	GTCAAACCCATCTGA[C/T]TCATTCACTTCCTAT	127544
rs763599254	snp	A/G	1.64914e-05	0.00287149	synonymous-codon, intron-variant	RNF19B	GRCh38.p7	1:32938510	AATTTCCTTTTGGAC[A/G]TCGGCTTGAACTTCT	127544
rs763664843	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32942619	AACATATGTTCATAT[G/T]TAATCCTCCAAATAA	127544
rs763794285	in-del	-/A	1.65868e-05	0.00287978	intron-variant	RNF19B	GRCh38.p7	1:32948382	TATGAGTGGGGGAAG[-/A]AATGGGTAGAAAAAA	127544
rs763816230	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32963070	GGGTTCAGAAACACA[A/G]TTTCTCCTATCACAC	127544
rs763988763	snp	G/T	3.30115e-05	0.00406259	synonymous-codon	RNF19B	GRCh38.p7	1:32944026	CTTTTTACCTGTGAT[G/T]GGACCATCATCTTCA	127544
rs763989602	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32951368	TGGCACAGCCCACGG[A/G]GCAGCAGGAGCAGCA	127544
rs764077419	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32938775	TCATCTCCTGCCTGG[A/G]TGACTAAAACTGGGC	127544
rs764088287	snp	C/T	6.69266e-05	0.00578436	synonymous-codon	RNF19B	GRCh38.p7	1:32942458	TCTCCAGGCATCTGC[C/T]ACTGGGGATAGAACC	127544
rs764175068	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32935850	CTCCCCAGGCTCAAG[C/T]GCTTCTCCTGCCACA	127544
rs764218663	snp	A/G	1.69812e-05	0.00291382	intron-variant	RNF19B	GRCh38.p7	1:32946362	TTTACTAACGAACCT[A/G]AAGTTGAAACAAGCA	127544
rs764234534	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32960288	CACATGCCCCCCTCA[C/G]CCTACCAAATGCACA	127544
rs764275409	snp	C/G	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937001	CTGTGCATCAGAACT[C/G]TCTAGGTCACTGCGG	127544
rs764289803	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32935100	CTCCCAAAGTGCTGG[C/G]ATTGCAGGTGTGAAC	127544
rs764336495	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32963385	ATTCTCATTCCCTCC[C/T]TGGCCAAATATCCCC	127544
rs764410886	in-del	-/TAC			intron-variant	RNF19B	GRCh38.p7	1:32952584	TGTCTCTACTAAAAA[-/TAC]AAAAAATTAGCTGGG	127544
rs764615008	snp	A/T	1.6582e-05	0.00287936	missense	RNF19B	GRCh38.p7	1:32942260	TGTTTACCTGCTATA[A/T]TTTCCCTTGCCACTG	127544
rs764643132	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32954971	TTGCCCTGACAAGTA[C/T]CCATTTAAGAACCAA	127544
rs764676234	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32939098	AAACTTATACTCAGT[C/G]CTTAACAACAAAGGA	127544
rs764851529	snp	A/G	6.60175e-05	0.00574494	synonymous-codon	RNF19B	GRCh38.p7	1:32949756	GCAGCTGGCACAGCC[A/G]TAGGCAATAACAGCA	127544
rs764925951	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32954044	CTCCCAAGTAGCTGG[A/G]CTTACAGGCGCCCGC	127544
rs764941807	snp	C/G	1.64727e-05	0.00286986	missense	RNF19B	GRCh38.p7	1:32949641	AAGTCTGGGCCCTCT[C/G]TTGACGGGCCATATC	127544
rs764993533	snp	A/C	1.66076e-05	0.00288158	intron-variant	RNF19B	GRCh38.p7	1:32938537	TTCTAACCTGTGTAA[A/C]GAGGGGACGTTCAAG	127544
rs765038310	in-del	-/T			intron-variant	RNF19B	GRCh38.p7	1:32949997	GAGACAGTCTTGCTC[-/T]TGTCACCCAGGCTGG	127544
rs765050430	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32940119	GAGGGAATGCAATGG[A/G]AAGTGCACAGTGTCA	127544
rs765082059	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32960691	AACCATGACATCCAG[G/T]AAGAACACAGAAGCT	127544
rs765304166	snp	C/T	0.000102907	0.00717238	missense	RNF19B	GRCh38.p7	1:32964349	CCACCTCCTCCGCGC[C/T]CGGGCCACCGCCCTC	127544
rs765459967	snp	C/G			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933018	CCAACCTGGTCATGT[C/G]AAGTAGCACTATCTA	127544
rs765527865	snp	C/T			utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937131	CCTCCGCCACCACTA[C/T]CTTCTTCTTCATTCT	127544
rs765616862	snp	A/G	1.64781e-05	0.00287033	utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32937265	GTTGCATTCTCTGTG[A/G]AGACAAAATCCACTT	127544
rs765651717	snp	C/T	1.68471e-05	0.00290228	synonymous-codon	RNF19B	GRCh38.p7	1:32946534	CTTACGGCTCCATGG[C/T]TTCTTGCCCCAGAAT	127544
rs765662387	snp	A/G			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933989	GAATTGTTCTCTCGA[A/G]GCTTCAAGAGAATTC	127544
rs765710484	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32942640	CTCCAAATAACTAGG[A/C]ATTAATAGCCTCAAT	127544
rs765710618	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32957403	TTATCATATGACATT[C/T]GAATAATTTTCTATC	127544
rs765886239	snp	C/T	1.69476e-05	0.00291093	intron-variant	RNF19B	GRCh38.p7	1:32946372	AACCTAAAGTTGAAA[C/T]AAGCACAGAAACCAG	127544
rs765898779	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32934873	AGTCTCACTCTGTCA[C/G]CCAGGCTGGAGTGCA	127544
rs766001797	snp	C/T	1.64974e-05	0.00287201	missense	RNF19B	GRCh38.p7	1:32942420	TCAATGCTGCTTTCC[C/T]CAATGCTGGGATTCT	127544
rs766106019	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32953740	CTTGTTATTTTGCAT[C/T]AAATGGGAAAGTTAC	127544
rs766197367	snp	A/C	3.29881e-05	0.00406115	missense	RNF19B	GRCh38.p7	1:32942285	CCACTGGAGAGAATG[A/C]CGCCACTCAGCGTGC	127544
rs766225456	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32949788	AACTAGGTAAGGAAA[C/T]AGTAAGAGATACCAG	127544
rs766434824	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32958406	TGTGAGTGAAAAATA[C/G]AAAATAAAATCAAAA	127544
rs766447585	snp	C/G	1.65176e-05	0.00287376	intron-variant	RNF19B	GRCh38.p7	1:32945469	TGGCTAAACTGCTAT[C/G]GTCAGAAAGCTGAGA	127544
rs766457456	in-del	-/CCG	0.0215431	0.101526	cds-indel	RNF19B	GRCh38.p7	1:32964393	CGTCGAACCCAGGCT[-/CCG]CCGCCGCCGCCGCCG	127544
rs766479633	in-del	-/A			intron-variant	RNF19B	GRCh38.p7	1:32955167	TTTTTAATCTCAGTC[-/A]TAGTATACTGGTTCA	127544
rs766485902	snp	G/T	1.73321e-05	0.00294376	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936857	AGTTTGTCCCTCGGC[G/T]AGGGCAGAGAGGTTC	127544
rs766513625	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32957618	GCGGGTGGCTCGCTT[G/T]AAGTCAGGAATTCAA	127544
rs766809205	snp	A/C			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967161	CACTGGATTTGGCAA[A/C]ACCAAAGAGTCCTAA	127544
rs766844553	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933080	TTACTTATCCTCACT[C/T]CAGGTTATATATCTG	127544
rs766859392	snp	C/T	3.50226e-05	0.0041845	intron-variant	RNF19B	GRCh38.p7	1:32938314	ATGGTACATACAGCC[C/T]TAACATGAGGCATTG	127544
rs766932602	snp	A/G			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32934260	AGTAAAACACTGGCC[A/G]GGAAGACAAAAGTGC	127544
rs766940161	snp	A/G	8.57537e-05	0.00654748	intron-variant	RNF19B	GRCh38.p7	1:32937319	CTAAACCTGTTGGTA[A/G]AAGCAGTTCATGGGT	127544
rs766964815	snp	C/G	1.64749e-05	0.00287005	missense	RNF19B	GRCh38.p7	1:32948260	CTCTTTCATACAAAG[C/G]CAACAGAATTCACAG	127544
rs766975382	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32961860	GACTTTAGAAAAATA[A/G]AAAAACAAACAGGGA	127544
rs767004567	snp	C/T			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965598	GAGGCAGGCAAACAG[C/T]TTCAACAACAGGAAT	127544
rs767016377	snp	C/T	1.66735e-05	0.00288729	intron-variant	RNF19B	GRCh38.p7	1:32948400	TGGGTAGAAAAAATA[C/T]CCCTAGTTAAATCCA	127544
rs767251568	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32941410	CCAGGCATGGTGGTG[C/T]ACGCCTGTAGTCCCA	127544
rs767296409	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32963816	CTGTCTCCTAACTTG[A/G]ACAGCTCCCTTCCCC	127544
rs767338461	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32948989	TGAATGGCAAAATCT[C/T]TCCTACTAGCCTCTC	127544
rs767339468	snp	A/G	1.7865e-05	0.00298867	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936832	CTTCTCCACCTTCTG[A/G]CTTCAAGACAGTTTG	127544
rs767402214	snp	C/G	0.000133699	0.00817505	missense	RNF19B	GRCh38.p7	1:32964259	GGCGGAGGCAGTCCC[C/G]GCACGAGCGGTGCGG	127544
rs767420751	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32962886	ACTGACAGTAACAAT[C/T]AGACTTCTAAAGGCG	127544
rs767545315	snp	A/G	5.11139e-05	0.00505513	intron-variant	RNF19B	GRCh38.p7	1:32946356	CAAACCTTTACTAAC[A/G]AACCTAAAGTTGAAA	127544
rs767561126	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32950028	ATTGTGGAGTGCAGT[A/G]GTGTAATCTCGGCTT	127544
rs767594434	snp	A/C	1.6473e-05	0.00286988	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936995	GTCTGACTGTGCATC[A/C]GAACTCTCTAGGTCA	127544
rs767698525	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32945900	TTTTTTTGGAGTCTG[C/T]CATGCAGGCTGGAGT	127544
rs767743653	in-del	-/A			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966973	TCAAACTTTTGACAT[-/A]AAACAAGAAGGGGAG	127544
rs767772345	snp	A/G	1.64798e-05	0.00287047	synonymous-codon	RNF19B	GRCh38.p7	1:32945518	GACTAGCTTACCAAC[A/G]CTAACTGCAGCAATA	127544
rs768014132	in-del	-/GC	0.00011533	0.00759287	utr-variant-3-prime, frameshift-variant	RNF19B	GRCh38.p7	1:32936937	GGCTGCAGTATGGGA[-/GC]GCGGGGGGAGCCACA	127544
rs768125775	snp	A/G	1.66593e-05	0.00288607	intron-variant	RNF19B	GRCh38.p7	1:32938331	AACATGAGGCATTGA[A/G]CTTCTGAAGACCTAG	127544
rs768161540	snp	C/T	1.64822e-05	0.00287068	synonymous-codon	RNF19B	GRCh38.p7	1:32949738	CTCACAAGTTAGCTT[C/T]GGGCAGCTGGCACAG	127544
rs768188822	snp	C/G	3.29462e-05	0.00405857	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937046	GGCCAGGCTGATGTC[C/G]CAAGGTTTGCTGGCC	127544
rs768234916	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32934406	AATCTGAGGGCCGGG[C/T]GAGGTGGCTCATGCC	127544
rs768250614	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32945353	ATAATTTGGTGTGCT[C/T]GAAAAACTTAAAAAT	127544
rs768254664	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32959122	CTAGGGATGAAAAAA[C/G]CTTCCTGTTTATGGG	127544
rs768261133	snp	A/G	1.6473e-05	0.00286988	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936968	CTCATCTGAGGTGAT[A/G]TCTGGCACATCGTCT	127544
rs768352750	snp	C/T	0.000182293	0.00954532	synonymous-codon	RNF19B	GRCh38.p7	1:32945617	TTTCCTTCCCTCATA[C/T]CTGCTGTGAATCTAA	127544
rs768380161	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32940020	AGCTGCACATTCAAG[C/T]AGCTTCCATCCTACT	127544
rs768462572	snp	A/G	3.40652e-05	0.00412691	intron-variant	RNF19B	GRCh38.p7	1:32944201	GCTGGCTATTAGGTT[A/G]CAAGTGCCCTGAATT	127544
rs768470139	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32940973	TCATGCCTATAATCC[C/T]AGCACGTTGGGAGCC	127544
rs768504177	in-del	-/C			intron-variant	RNF19B	GRCh38.p7	1:32939408	GCCAGGCTGGTCTTG[-/C]AACTCTAAACCTCAG	127544
rs768579851	snp	A/G	4.96167e-05	0.00498055	intron-variant	RNF19B	GRCh38.p7	1:32948206	ACGAAAGGAATGGAT[A/G]CATTTCCCATCTTAC	127544
rs768632738	snp	C/G	1.64735e-05	0.00286993	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937237	CTTCAATGTCCACTT[C/G]GATTTCCATATTGTT	127544
rs768794710	snp	C/T			missense	RNF19B	GRCh38.p7	1:32949754	GGGCAGCTGGCACAG[C/T]CATAGGCAATAACAG	127544
rs768797972	snp	A/G	1.64969e-05	0.00287196	synonymous-codon	RNF19B	GRCh38.p7	1:32948356	TCGTGGGCATGGCTT[A/G]ATGTCATCTGCTATG	127544
rs768801633	snp	A/G	1.8249e-05	0.00302062	utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32936760	AAAAAATTCCAAAAG[A/G]TGCAGTTACAAGTGT	127544
rs768841592	in-del	-/G	1.6495e-05	0.0028718	intron-variant	RNF19B	GRCh38.p7	1:32938375	AATGCAACCTCTCCT[-/G]GACATCTGACTGTTC	127544
rs768884973	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32950990	GACTATAGGCATGCA[C/T]CACCATGCGCAGCTA	127544
rs768981506	snp	C/G	1.64762e-05	0.00287016	missense	RNF19B	GRCh38.p7	1:32942381	GTAGGGCTTCCACTA[C/G]TGCTCAATACACTAG	127544
rs769012759	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32957047	AAATTCCATTCTGGA[A/G]GGTTACTCTTTTGCT	127544
rs769198911	snp	C/G	0.000269505	0.0116052	missense	RNF19B	GRCh38.p7	1:32964580	CAGAGAAGACGCTGT[C/G]CAAGGTGAGGCGCCG	127544
rs769214241	snp	A/T	1.69315e-05	0.00290955	intron-variant	RNF19B	GRCh38.p7	1:32942244	TCAGAAATTATCTAT[A/T]TGTTTACCTGCTATA	127544
rs769245660	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32959999	GAGCTTGCACTGAGC[A/T]GAGATGGTGCCACTG	127544
rs769332299	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32938024	AGAGAAAGAAGCTAT[A/G]GGAATCCTATCAAGC	127544
rs769347595	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32935250	TCAAGCGATTCTCCT[A/G]CCTCAGCCTCCCGAG	127544
rs769356232	snp	A/C	1.64838e-05	0.00287083	missense	RNF19B	GRCh38.p7	1:32942402	AATACACTAGTCAGG[A/C]CTTCAATGCTGCTTT	127544
rs769368028	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32955999	CTTTGTCAGGCAAAG[A/G]CAGGAGGATCACTTG	127544
rs769385154	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32934926	CAACATCCGCCTCCC[A/G]AGTTCAAGTGATTCT	127544
rs769495333	snp	C/T	1.64727e-05	0.00286986	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937089	TGTTCACAGCTTTGG[C/T]GTCTGCAGGGGGGAT	127544
rs769543687	snp	A/C	1.65638e-05	0.00287778	synonymous-codon	RNF19B	GRCh38.p7	1:32946417	CTTCCTTCCAACATA[A/C]ACAGGAATGCCAATG	127544
rs769572063	snp	A/G			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32967030	GCCAGTGACATAAAA[A/G]AAAAACTAAGCAGGC	127544
rs769599278	snp	C/T	1.64735e-05	0.00286993	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936979	TGATGTCTGGCACAT[C/T]GTCTGACTGTGCATC	127544
rs769696438	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32952567	CCAACATGGTGAAAC[A/G]CTGTCTCTACTAAAA	127544
rs769739298	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32954658	CAGGAGAATTGCTTG[A/G]AACTGGGAGGCGGAG	127544
rs769779097	snp	A/G	2.07851e-05	0.00322368	intron-variant	RNF19B	GRCh38.p7	1:32945670	TCAGCAGGTTAGGAC[A/G]TCAATCTTTTGCCAG	127544
rs769791367	snp	A/G			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933933	GTTTAGCCATAAACT[A/G]CTGCCCCTCCAACAG	127544
rs769823171	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32941088	TGTTAGCTGGGTGTG[A/G]TGTGTGCACTTGTAG	127544
rs769932793	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32938643	TGGTTGTCTGTCTGA[A/T]CTTCTCCAACTGTCA	127544
rs769959395	snp	A/G	1.64743e-05	0.00287	synonymous-codon	RNF19B	GRCh38.p7	1:32949588	TCCAGATTCTTGCCC[A/G]TAACTGAGACCTGAA	127544
rs769965690	snp	A/C	6.46907e-05	0.00568693	intron-variant	RNF19B	GRCh38.p7	1:32938294	TACACTATATATCCC[A/C]GGAGATGGTACATAC	127544
rs770012748	snp	C/T	1.64798e-05	0.00287047	missense, intron-variant	RNF19B	GRCh38.p7	1:32938412	CTGTCCTGTGGGTTG[C/T]AGGAACTGATTATGG	127544
rs770020658	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32939778	CAGTCAAACCCATCT[A/G]ACTCATTCACTTCCT	127544
rs770027708	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32963624	TCGGGAGGCTGAGGC[A/T]GGAGAATCGCTTGAA	127544
rs770083621	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32945499	AGAGAAGAGGTGTGG[A/T]CCTGACTAGCTTACC	127544
rs770120592	snp	A/G	9.07581e-05	0.00673579	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32936789	GTGCTTCTCAGAACA[A/G]GAGCATTCATTCCAC	127544
rs770177839	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32946795	TCCAGACTTGAAATT[C/T]CTTTTCCATTCTTCT	127544
rs770291681	snp	A/G	1.651e-05	0.0028731	intron-variant	RNF19B	GRCh38.p7	1:32948215	ATGGATGCATTTCCC[A/G]TCTTACCTGAGGTAA	127544
rs770356946	in-del	-/AAAG			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966456	AAAAAAGAAAAAGAA[-/AAAG]AAAGAAAGAAAAAAG	127544
rs770385076	in-del	-/G	1.64942e-05	0.00287173	intron-variant	RNF19B	GRCh38.p7	1:32945496	AGAGAGAAGAGGTGT[-/G]GGTCCTGACTAGCTT	127544
rs770441118	in-del	-/A			intron-variant	RNF19B	GRCh38.p7	1:32945273	AAGTTTCTGTAATTC[-/A]ACCTTTTCTATGTGC	127544
rs770442656	snp	A/C	3.36468e-05	0.0041015	intron-variant	RNF19B	GRCh38.p7	1:32943982	TTTTATCTTGTATAT[A/C]ATAAATTCAAATGGA	127544
rs770508427	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32955411	AAGTTCTGAATACGG[C/T]AATCTTCTTCCCGAA	127544
rs770585952	snp	A/C/G	0.000332198	0.0128839	intron-variant	RNF19B	GRCh38.p7	1:32944166	CACCAATACCTGGGG[A/C/G]AAGAGAAGGAAACAT	127544
rs770596366	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32956678	TTTATTAATTTCCTA[A/C]ATCTTCAGAAACTTC	127544
rs770763845	snp	C/G	0.000265006	0.0115079	utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964699	ATGGCCGGCAGAGGC[C/G]GAGGAGCCAGGGGCG	127544
rs770840349	in-del	-/CAAT			intron-variant	RNF19B	GRCh38.p7	1:32955874	CTCTTTTAGCTTAAC[-/CAAT]CAGTCAGGCTTGCTA	127544
rs770919919	snp	A/G	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937101	TGGTGTCTGCAGGGG[A/G]GATCCTCTTCACTGC	127544
rs770959736	snp	C/T	6.6433e-05	0.00576299	intron-variant	RNF19B	GRCh38.p7	1:32948190	GTAAGAGAATGAGAC[C/T]ACGAAAGGAATGGAT	127544
rs771111232	snp	A/T	3.36315e-05	0.00410057	intron-variant	RNF19B	GRCh38.p7	1:32938573	ATGAGACCTGGGTAT[A/T]CCAAGACAGTCTGCT	127544
rs771157444	snp	A/G	1.65868e-05	0.00287978	intron-variant	RNF19B	GRCh38.p7	1:32948382	CTATGAGTGGGGGAA[A/G]AATGGGTAGAAAAAA	127544
rs771233535	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32939979	CCAGAGTCATGAGAT[G/T]CACAGACGGGTCAGT	127544
rs771273704	snp	C/G	8.33104e-05	0.00645355	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936887	CATATGGGCACTTGG[C/G]CTCGGTGCACCTTGG	127544
rs771308227	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32935435	TGAGCCACTGTGCCC[A/G]GCCAGGACATTATTT	127544
rs771312580	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32959724	GATTATACTAGGCCA[C/T]ATTGTTCTTAGTATA	127544
rs771339525	snp	A/G	0.000131776	0.00811608	synonymous-codon	RNF19B	GRCh38.p7	1:32949597	TTGCCCATAACTGAG[A/G]CCTGAAGTGTGTTTG	127544
rs771346303	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	RNF19B	GRCh38.p7	1:32938451	ATAGCACGAGTGCTT[A/G]CGTTGTCACTAATTG	127544
rs771395591	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32962374	TCACTAGACATAGAC[A/C]GTTCCATGAACCTAA	127544
rs771489195	in-del	-/C			intron-variant	RNF19B	GRCh38.p7	1:32953351	TCCTCTATTCCAATA[-/C]TCTCCCGCAATATTC	127544
rs771490054	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32946952	AACACTCTGATTTGT[G/T]TAGTTTTCTTGGCAT	127544
rs771528314	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32959820	AGGTGGGCAGATCAC[A/G]AGGTCAGGAGATCGA	127544
rs771642991	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32943238	ACGAGTAGAAACCAC[A/G]TTAAAGTAAAAGTCA	127544
rs771682752	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32956902	CATCAGGGTGGTAGA[C/T]ATGCGCCAACTTGTC	127544
rs771728114	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32955679	GCTACAGCCCGGGAG[G/T]TGGAGGCTGCAGTGA	127544
rs771730554	in-del	-/T	2.20811e-05	0.00332266	intron-variant	RNF19B	GRCh38.p7	1:32945677	GTTAGGACATCAATC[-/T]TTTGCCAGAGAAAAA	127544
rs771730609	snp	A/C			downstream-variant-500B	RNF19B	GRCh38.p7	1:32932472	CTTGACCTTAGGTTA[A/C]ATTCAGAACCTTGGT	127544
rs771734740	snp	A/C	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936951	GAGCGGGGGGAGCCA[A/C]ACTCATCTGAGGTGA	127544
rs771796670	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32951303	CCCACGTCAGGCATA[A/G]CAGTTGCACTTCTCC	127544
rs771908590	snp	C/T	5.28011e-05	0.00513788	intron-variant	RNF19B	GRCh38.p7	1:32944181	GAAGAGAAGGAAACA[C/T]GTCAGCTGGCTATTA	127544
rs772007245	in-del	-/AAAAA			intron-variant	RNF19B	GRCh38.p7	1:32952431	AGACCTTTTCTCTTA[-/AAAAA]AAAAAAAAAAAAAAA	127544
rs772026184	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32941958	AAAAATTAGCTGGGC[A/G]TGGTGGCGGGTGCCT	127544
rs772058503	snp	A/G	4.99397e-05	0.00499673	missense	RNF19B	GRCh38.p7	1:32946493	GGAGCACCAATCAAC[A/G]TGCCCAGCTGCCAAA	127544
rs772068170	snp	A/C			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965008	GGTTCCAGGGCCGCC[A/C]TGTTGCGGAGACTCT	127544
rs772108227	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32951476	AGGAGCAGTTGGGGT[C/T]CATTTCGAGCAAAGG	127544
rs772118551	snp	G/T	1.64874e-05	0.00287113	intron-variant	RNF19B	GRCh38.p7	1:32938277	CAAATGAATTCACAG[G/T]TTACACTATATATCC	127544
rs772184591	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933727	TAAAATCTCCTTTAA[C/T]TCATTTCTTCTTCTT	127544
rs772223455	snp	A/G/T			intron-variant	RNF19B	GRCh38.p7	1:32961369	TGCTTTTTAAAACAG[A/G/T]GGCTGAATGGAAGGA	127544
rs772291724	snp	C/T	3.29478e-05	0.00405867	missense, intron-variant	RNF19B	GRCh38.p7	1:32938464	TTGCGTTGTCACTAA[C/T]TGCACCAAGACTGGC	127544
rs772386865	snp	A/G	1.64792e-05	0.00287042	synonymous-codon	RNF19B	GRCh38.p7	1:32949729	ACCTTCCCTCTCACA[A/G]GTTAGCTTCGGGCAG	127544
rs772413607	in-del	-/A			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965611	AGCTTCAACAACAGG[-/A]ATGTATCAGGATTAC	127544
rs772414779	snp	A/G			utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32936501	TCAGTAATATGTTTA[A/G]CATTCAATATACACA	127544
rs772451719	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32956236	GCTGGGCATGGTGGC[A/G]TGCACTTGTAGTCCC	127544
rs772500341	snp	A/C	3.49205e-05	0.0041784	intron-variant	RNF19B	GRCh38.p7	1:32942213	GTGTTACTTCTTATA[A/C]TTCTAACCATTTCTG	127544
rs772511651	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32935682	ATTGCTTTGTGATTA[C/T]GCGCATCAGTGTATT	127544
rs772527754	snp	A/G	3.29739e-05	0.00406028	missense	RNF19B	GRCh38.p7	1:32942408	CTAGTCAGGCCTTCA[A/G]TGCTGCTTTCCCCAA	127544
rs772625181	snp	C/T	1.64727e-05	0.00286986	missense	RNF19B	GRCh38.p7	1:32949616	GAAGTGTGTTTGGTC[C/T]GAACTCGTAAAGTCT	127544
rs772646181	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32954670	TTGAAACTGGGAGGC[A/G]GAGGTTGCAGTGAGC	127544
rs772692227	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32949477	TGATCCTTTGGAGTA[A/C]TTGGGTTATACAATA	127544
rs772886371	snp	A/G	3.31697e-05	0.00407231	synonymous-codon	RNF19B	GRCh38.p7	1:32949771	ATAGGCAATAACAGC[A/G]TAACTAGGTAAGGAA	127544
rs772933089	snp	G/T	1.64727e-05	0.00286986	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937098	CTTTGGTGTCTGCAG[G/T]GGGGATCCTCTTCAC	127544
rs773015895	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32941103	GTGTGTGCACTTGTA[C/G]TCCTAGCTACTCAGG	127544
rs773106988	snp	C/T	1.704e-05	0.00291885	intron-variant	RNF19B	GRCh38.p7	1:32946352	CCCTCAAACCTTTAC[C/T]AACGAACCTAAAGTT	127544
rs773164054	snp	A/G	1.64732e-05	0.0028699	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936980	GATGTCTGGCACATC[A/G]TCTGACTGTGCATCA	127544
rs773306371	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32951177	AAATTGTTTTATTGT[C/T]ATTAACATATTTAAT	127544
rs773448687	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32940281	GCTTTTGCAAAACAC[A/G]GATCACCCCCTAGGT	127544
rs773486216	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32934217	ATCTTCTAAGCTGGC[C/T]GTTGTCCAGACTTGC	127544
rs773549167	snp	C/G	0.000115372	0.00759424	utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32937276	TGTGGAGACAAAATC[C/G]ACTTTGCTGAGTCAT	127544
rs773570654	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32959179	GCCAATAGCTGATAC[C/T]GTTTCCTGGGATCAG	127544
rs773610109	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32946841	TTCCCTAACCCACCA[A/C]AACTGATCTAGCTTC	127544
rs773640807	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32958311	TTTTATTTTGTTTAA[C/T]TCAGTATTTTCCAAG	127544
rs773732572	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32959441	ACAGTTACCTGACTT[C/T]GGGGTTTCTGAAAAG	127544
rs773748872	snp	A/C	1.81401e-05	0.0030116	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32936793	TTCTCAGAACAGGAG[A/C]ATTCATTCCACTTCA	127544
rs773782530	snp	C/T	1.65037e-05	0.00287256	intron-variant	RNF19B	GRCh38.p7	1:32948218	GATGCATTTCCCATC[C/T]TACCTGAGGTAATGC	127544
rs773921815	in-del	-/T			intron-variant	RNF19B	GRCh38.p7	1:32945804	GGAAGATATAAAGTA[-/T]ATACAGGCAAAGTTA	127544
rs773970586	in-del	-/T	1.75786e-05	0.00296462	intron-variant	RNF19B	GRCh38.p7	1:32945636	CTGTGAATCTAAGAA[-/T]AAAAAAAGAAAATCC	127544
rs774047726	snp	A/G			synonymous-codon	RNF19B	GRCh38.p7	1:32942275	TTTTCCCTTGCCACT[A/G]GAGAGAATGCCGCCA	127544
rs774082139	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32954857	ATGTGAGACCTTGTC[C/G]TCAAAGATATATGGC	127544
rs774124941	snp	C/T	0.000474046	0.0153883	utr-variant-5-prime	RNF19B	GRCh38.p7	1:32964713	CCGAGGAGCCAGGGG[C/T]GCCCAGCGCCGCCAC	127544
rs774125071	snp	A/G	3.30022e-05	0.00406202	missense	RNF19B	GRCh38.p7	1:32942423	ATGCTGCTTTCCCCA[A/G]TGCTGGGATTCTTGA	127544
rs774134285	snp	C/T	3.32204e-05	0.00407542	intron-variant	RNF19B	GRCh38.p7	1:32948192	AAGAGAATGAGACTA[C/T]GAAAGGAATGGATGC	127544
rs774170023	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32955423	CGGTAATCTTCTTCC[C/T]GAATAGTTGGAAAAA	127544
rs774304731	snp	A/G	1.64741e-05	0.00286998	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937210	TCACCAGCTGATAGT[A/G]GCTTGGTTTGGCTTC	127544
rs774351862	snp	A/G			downstream-variant-500B	RNF19B	GRCh38.p7	1:32932321	AACACCCACAAAGCT[A/G]CTGATGGCTATTAGA	127544
rs774352642	snp	A/G	0.000116003	0.00761497	missense	RNF19B	GRCh38.p7	1:32964210	GGGCAGCTGATGGGC[A/G]CCCTGCTCTCGCTTA	127544
rs774416215	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32963484	ACTTTGGGAGGCCGA[A/G]GCAGGAGGATCACCT	127544
rs774418055	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32943196	CTTTGGGGTTTTCTA[C/T]GTTACTTGTGCCCTA	127544
rs774422629	snp	A/G	1.64743e-05	0.00287	synonymous-codon, intron-variant	RNF19B	GRCh38.p7	1:32938453	AGCACGAGTGCTTGC[A/G]TTGTCACTAATTGCA	127544
rs774424732	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32939988	TGAGATGCACAGACG[C/G]GTCAGTAGCAGCCTG	127544
rs774431882	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32940043	ATCCTACTGCCTGAG[C/G]CTTTGCTTTGCTGCT	127544
rs774452881	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32948927	GCAAGTTATGAACTA[G/T]CCTAATAAAATGACA	127544
rs774468155	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32958443	TGGAGATGGCCGGGC[G/T]TGGTGGCTCACGCCT	127544
rs774511302	snp	A/C	0.000115305	0.00759205	missense	RNF19B	GRCh38.p7	1:32949598	TGCCCATAACTGAGA[A/C]CTGAAGTGTGTTTGG	127544
rs774543463	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32959735	GCCATATTGTTCTTA[C/G]TATATTAAATAATAA	127544
rs774659865	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32935566	CCTTTCATTACAAAT[C/T]TCAGATTTTAGTCCC	127544
rs774734364	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32948140	CTGTAATGAGAGAAC[A/G]GATGTGTCTTTTTGA	127544
rs774752528	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32941873	GAGGCCAAGGCGGGC[A/G]GATCACGAGGTCAGG	127544
rs774911417	snp	C/T	1.66618e-05	0.00288628	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936888	ATATGGGCACTTGGG[C/T]TCGGTGCACCTTGGG	127544
rs774917780	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32946953	ACACTCTGATTTGTG[C/T]AGTTTTCTTGGCATA	127544
rs774968412	snp	A/C			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32934236	GTCCAGACTTGCCAT[A/C]CTCATTGTAGTAAAA	127544
rs775039959	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32962894	TAACAATTAGACTTC[C/T]AAAGGCGGGGAGGGC	127544
rs775148055	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32956024	CACTTGAACCCAAGA[G/T]TTCAAGACCAGCCAG	127544
rs775225481	in-del	-/G	1.65143e-05	0.00287348	intron-variant	RNF19B	GRCh38.p7	1:32945681	GGACATCAATCTTTT[-/G]CCAGAGAAAAAAAGG	127544
rs775263133	snp	A/G	1.77332e-05	0.00297763	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936842	TTCTGGCTTCAAGAC[A/G]GTTTGTCCCTCGGCT	127544
rs775280388	snp	A/G	2.34882e-05	0.00342689	intron-variant	RNF19B	GRCh38.p7	1:32938282	GAATTCACAGGTTAC[A/G]CTATATATCCCAGGA	127544
rs775297331	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32943291	TCTGTGAAGCTCTTA[A/C]TAGATAGTAAGATGA	127544
rs775317758	snp	A/G	0.000199243	0.00997907	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936891	TGGGCACTTGGGCTC[A/G]GTGCACCTTGGGCTC	127544
rs775343090	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	RNF19B	GRCh38.p7	1:32965065	TGGTCTCCGCCTCCA[A/G]TTCCATCACCATGAC	127544
rs775396752	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32938700	TTTTTCTCTTAAATA[G/T]CTATTGAAATCGTCC	127544
rs775493887	snp	C/T	1.66164e-05	0.00288235	intron-variant	RNF19B	GRCh38.p7	1:32944007	AATGGAAATAAACAT[C/T]CTGCTTTTTACCTGT	127544
rs775503919	in-del	-/G			intron-variant	RNF19B	GRCh38.p7	1:32934340	TTCAATTTTTCCTCT[-/G]GGCCCAGGACTAAGG	127544
rs775554828	snp	A/G			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933905	GTAAGTGGAACCCAG[A/G]TAAGAAATATAGGTT	127544
rs775597353	snp	A/T	1.69989e-05	0.00291533	intron-variant	RNF19B	GRCh38.p7	1:32946357	AAACCTTTACTAACG[A/T]ACCTAAAGTTGAAAC	127544
rs775599423	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32947151	ACTAGAAGGGATAAA[C/G]AATTTTGAAAATAGG	127544
rs775650669	snp	C/T	1.73567e-05	0.00294586	intron-variant	RNF19B	GRCh38.p7	1:32942223	TTATAATTCTAACCA[C/T]TTCTGTCAGAAATTA	127544
rs775791882	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32960083	AATGTGAATGTTTTC[C/T]CACTGAAATTGGTTC	127544
rs775873222	snp	C/T			utr-variant-3-prime, intron-variant	RNF19B	GRCh38.p7	1:32936535	ACATATGTACACTCT[C/T]TGACACACCTCATGG	127544
rs775945827	snp	C/G	1.64727e-05	0.00286986	missense	RNF19B	GRCh38.p7	1:32949617	AAGTGTGTTTGGTCC[C/G]AACTCGTAAAGTCTG	127544
rs776001052	snp	A/G	1.64795e-05	0.00287045	missense	RNF19B	GRCh38.p7	1:32949730	CCTTCCCTCTCACAA[A/G]TTAGCTTCGGGCAGC	127544
rs776060740	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32935742	TCCAACTTGTAACCA[C/T]GCAACATTCACTGAG	127544
rs776073735	snp	A/G	1.64852e-05	0.00287094	synonymous-codon	RNF19B	GRCh38.p7	1:32949741	ACAAGTTAGCTTCGG[A/G]CAGCTGGCACAGCCA	127544
rs776089455	snp	G/T	4.94295e-05	0.00497115	missense, intron-variant	RNF19B	GRCh38.p7	1:32938497	TGTCTTTGGGGAAAA[G/T]TTCCTTTTGGACATC	127544
rs776135467	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32949486	GGAGTACTTGGGTTA[C/T]ACAATAAGATAATTT	127544
rs776141083	snp	A/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32932881	ACAGACTAAGGATGC[A/T]CTACCAAAGGGCCTT	127544
rs776173115	snp	A/T			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965361	AAGTCCAAATTTCTT[A/T]GTCTAGCATTCAGTG	127544
rs776223358	snp	A/G	3.30175e-05	0.00406296	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936908	TGCACCTTGGGCTCT[A/G]GGGGTCGAGGGGCAG	127544
rs776336557	snp	A/G	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936972	TCTGAGGTGATGTCT[A/G]GCACATCGTCTGACT	127544
rs776338900	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32945368	TGAAAAACTTAAAAA[C/T]AATCATAATCATGGT	127544
rs776356852	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933973	ATTTTATCAAAGAAG[C/T]GAATTGTTCTCTCGA	127544
rs776360908	snp	G/T	1.64735e-05	0.00286993	missense	RNF19B	GRCh38.p7	1:32949631	CGAACTCGTAAAGTC[G/T]GGGCCCTCTGTTGAC	127544
rs776364841	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32952516	GGGACACTGAGGCAG[C/G]CAAGTCACAAGGTCA	127544
rs776423739	snp	C/T	1.67301e-05	0.00289219	missense	RNF19B	GRCh38.p7	1:32945622	TTCCCTCATACCTGC[C/T]GTGAATCTAAGAATA	127544
rs776448936	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32941004	AAGTTGGGAGGATGG[C/T]TTCAGGCCAGGAGTT	127544
rs776457529	snp	A/G	3.55815e-05	0.00421776	intron-variant	RNF19B	GRCh38.p7	1:32944205	GCTATTAGGTTGCAA[A/G]TGCCCTGAATTCTTC	127544
rs776545258	in-del	-/TTTGA	1.68628e-05	0.00290364	intron-variant	RNF19B	GRCh38.p7	1:32948417	CCTAGTTAAATCCAG[-/TTTGA]TTTAATTGTTCCTAG	127544
rs776650809	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32962293	TTAATATTCGTTTGG[C/T]TAAGAAAACAGATCA	127544
rs776711233	snp	A/G	1.64757e-05	0.00287012	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937255	TTTCCATATTGTTGC[A/G]TTCTCTGTGGAGACA	127544
rs776897052	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32934783	TGACATCAGGTTTCA[C/G]GAGTCTTCTAATTTT	127544
rs777018166	snp	G/T	1.65233e-05	0.00287426	intron-variant	RNF19B	GRCh38.p7	1:32948211	AGGAATGGATGCATT[G/T]CCCATCTTACCTGAG	127544
rs777104679	snp	C/T	1.67365e-05	0.00289275	splice-donor-variant	RNF19B	GRCh38.p7	1:32942251	TTATCTATTTGTTTA[C/T]CTGCTATATTTTCCC	127544
rs777173394	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32962526	CCATTTCTAAACAAG[C/T]TTGGCAGAATTAAAA	127544
rs777261099	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32938210	CTCTAAAAATCAAGC[A/G]CTAACAAGAAGAATC	127544
rs777281189	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32961944	AGAAAGGAGTTAATG[C/T]ACTATTCCAAAATTA	127544
rs777394832	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32942862	GCTAGAAAAACCGGC[C/T]GGGCGCGGTGGCTCA	127544
rs777397694	snp	A/G	3.29473e-05	0.00405864	missense	RNF19B	GRCh38.p7	1:32948285	TCACAGCCACACACT[A/G]CACAGGTCATGTGAT	127544
rs777407748	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32949202	GAGGCACTTAAGTCA[A/G]CTTGAAGGCAAACAG	127544
rs777413262	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32949337	TACTAAGAAAGTAGG[A/T]ACTACATAATTCAAT	127544
rs777484498	snp	A/G	1.66263e-05	0.00288321	intron-variant	RNF19B	GRCh38.p7	1:32948180	CCCTAAATCAGTAAG[A/G]GAATGAGACTACGAA	127544
rs777654443	snp	G/T	1.64727e-05	0.00286986	synonymous-codon	RNF19B	GRCh38.p7	1:32949669	ATCGCATGTCTGATT[G/T]GGATGCCATATCTGC	127544
rs777671855	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32957863	TGTTGAATTGAATGA[C/T]CACCTGTCTATACTA	127544
rs777873665	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32939932	AGTGAATATGCCAGC[A/C]TGTGGGGGCGGGATC	127544
rs777937908	snp	A/T	1.64789e-05	0.0028704	missense, intron-variant	RNF19B	GRCh38.p7	1:32938413	TGTCCTGTGGGTTGT[A/T]GGAACTGATTATGGA	127544
rs777947420	snp	C/T	5.0114e-05	0.00500545	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936884	GTTCATATGGGCACT[C/T]GGGCTCGGTGCACCT	127544
rs778148778	snp	C/G	1.64743e-05	0.00287	missense	RNF19B	GRCh38.p7	1:32945558	GCAATGACCGACAAA[C/G]TCACTCCTCCAGTGA	127544
rs778169741	snp	C/G	1.64732e-05	0.0028699	missense	RNF19B	GRCh38.p7	1:32949592	GATTCTTGCCCATAA[C/G]TGAGACCTGAAGTGT	127544
rs778182978	snp	A/G	1.76699e-05	0.00297231	synonymous-codon	RNF19B	GRCh38.p7	1:32944125	AATGGGCACAACCCC[A/G]TAAACATATGCCAGC	127544
rs778240699	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32961193	TTAGACCTATTTCAG[A/G]TAAGAAAAATAACGT	127544
rs778515814	snp	G/T			downstream-variant-500B, intron-variant	RNF19B	GRCh38.p7	1:32936320	ATAGATGACTACTGC[G/T]GTTGGATTTGAATAC	127544
rs778518078	snp	A/G	1.65209e-05	0.00287405	intron-variant	RNF19B	GRCh38.p7	1:32949549	AAATAAAGAGACAAT[A/G]AGATAATGCCAACTT	127544
rs778524434	snp	A/G			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933666	AAATTTAAATTTTTC[A/G]TAGCCTCTGGCCTAG	127544
rs778536255	snp	A/G	6.59903e-05	0.00574376	intron-variant	RNF19B	GRCh38.p7	1:32938366	CAACGAAAAAATGCA[A/G]CCTCTCCTGGACATC	127544
rs778540438	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32937776	TTTGCTGATTTAACT[A/G]TACATGCACACGTGT	127544
rs778611169	snp	A/T			intron-variant	RNF19B	GRCh38.p7	1:32956842	TCCATCCCCAAGTCA[A/T]GTAACATAACTAGGC	127544
rs778802299	snp	C/T	1.64754e-05	0.00287009	synonymous-codon	RNF19B	GRCh38.p7	1:32942326	GGCTGCAAAGCTGGC[C/T]GTTTCGCTGTAAGGA	127544
rs778840274	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32953220	TTCAAGCAACCCTCC[C/T]GCCTTAGCCTCCCAA	127544
rs778843452	in-del	-/CTG	6.58903e-05	0.00573941	utr-variant-3-prime, cds-indel	RNF19B	GRCh38.p7	1:32936969	CATCTGAGGTGATGT[-/CTG]CTGGCACATCGTCTG	127544
rs778983373	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32958020	CAGAGTTGTAGAAAT[A/G]GTTGGAATATAGATA	127544
rs779118497	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32955203	AAAATACCTGTGTTG[A/C]ATGAATGACAGAGAC	127544
rs779182218	snp	A/G	1.64738e-05	0.00286995	synonymous-codon	RNF19B	GRCh38.p7	1:32949705	GTGGTAGCAGAACTC[A/G]GTCTGGCAACCTTCC	127544
rs779233260	snp	A/C	5.05038e-05	0.00502487	intron-variant	RNF19B	GRCh38.p7	1:32938576	AGACCTGGGTATTCC[A/C]AGACAGTCTGCTTCC	127544
rs779491542	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32962074	CCTCACAGGTTCAAG[A/C]GATTCTGCCTCAGCC	127544
rs779552308	snp	C/T	1.6476e-05	0.00287014	missense	RNF19B	GRCh38.p7	1:32945583	CAGTGATAGCCAAAT[C/T]CCTCTTGTGTTTGGA	127544
rs779561180	snp	C/G	1.67601e-05	0.00289478	intron-variant	RNF19B	GRCh38.p7	1:32946387	CAAGCACAGAAACCA[C/G]CATGTCTTTCTTACC	127544
rs779580838	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32958929	GGAGGTTGGTGTACG[C/T]GCACAAGAGGAGGGG	127544
rs779608521	snp	C/G	1.64936e-05	0.00287168	missense	RNF19B	GRCh38.p7	1:32945606	TGTTTGGAGGTTTTC[C/G]TTCCCTCATACCTGC	127544
rs779651411	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32959012	GCCAAATCAAGAGAA[C/G]AGGTTCAGGGAGGCT	127544
rs779653345	snp	A/G	3.29457e-05	0.00405854	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32936963	CCACACTCATCTGAG[A/G]TGATGTCTGGCACAT	127544
rs779749165	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32944889	GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	127544
rs779785132	in-del	-/CA			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32966211	CCCAGGCTGGCGGAT[-/CA]CGAGGTCAGGAGATG	127544
rs779920661	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32938116	TTCCATGTAATTATA[A/C]ACTGTTGCAATAGCC	127544
rs780027556	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32946345	CCCATTTCCCTCAAA[A/C]CTTTACTAACGAACC	127544
rs780129968	snp	C/G	1.64781e-05	0.00287033	missense	RNF19B	GRCh38.p7	1:32949575	AACTTATACCTGGTC[C/G]AGATTCTTGCCCATA	127544
rs780144067	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32934621	GGGAGGCTGAGGTTG[C/T]AGTGTGCCAAAATCA	127544
rs780205603	in-del	-/AT	1.64746e-05	0.00287002	utr-variant-3-prime, frameshift-variant	RNF19B	GRCh38.p7	1:32937245	TCCACTTGGATTTCC[-/AT]ATTGTTGCATTCTCT	127544
rs780242013	snp	A/T	3.29473e-05	0.00405864	missense	RNF19B	GRCh38.p7	1:32942336	CTGGCCGTTTCGCTG[A/T]AAGGACCTTGCATAA	127544
rs780299146	snp	A/C	1.6998e-05	0.00291525	intron-variant	RNF19B	GRCh38.p7	1:32942472	CCACTGGGGATAGAA[A/C]CAAACATCCAATTCA	127544
rs780308655	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32956235	AGCTGGGCATGGTGG[A/C]GTGCACTTGTAGTCC	127544
rs780326103	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32962239	CTCCCAGAATGCTAG[A/G]ACTATAGGCGTGAGC	127544
rs780331855	snp	A/G	0.000227454	0.0106619	synonymous-codon	RNF19B	GRCh38.p7	1:32964068	GCAGTCCGGGGCCGG[A/G]CACCAGCGGCAGTCG	127544
rs780423174	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32937922	AAAGCTTTTTACTAC[C/T]ATGCCACAAGTAGAA	127544
rs780524682	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32952306	ACTTGTATAAAATAA[C/T]ATTTTAGCCAGGTGA	127544
rs780524725	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32934856	TTTATTTTGTCAGAC[A/G]GAGTCTCACTCTGTC	127544
rs780690670	snp	G/T	1.66585e-05	0.00288599	intron-variant	RNF19B	GRCh38.p7	1:32946398	ACCAGCATGTCTTTC[G/T]TACCTTCCTTCCAAC	127544
rs780704125	snp	A/G	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937035	CTTTCAGGCTGGGCC[A/G]GGCTGATGTCCCAAG	127544
rs780711266	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32947755	CTAGCCTCAAGATAC[G/T]TACAGTTTAGTAAGA	127544
rs780719037	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32946679	TAACAGAAGAGTTTA[C/T]GGGAAATGAATACAT	127544
rs780745942	snp	C/G	1.6473e-05	0.00286988	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937065	GGTTTGCTGGCCAGG[C/G]AGTCTTTCTGTTCAC	127544
rs780757574	snp	C/T	3.29451e-05	0.00405851	utr-variant-3-prime, missense	RNF19B	GRCh38.p7	1:32937167	ATCTGAGCATGAACA[C/T]GGAGCGAGTCCTCCG	127544
rs780818106	snp	A/C			intron-variant	RNF19B	GRCh38.p7	1:32959258	AGTGGTGGACCTGCA[A/C]AAAGAATTTAGGTCA	127544
rs780936067	snp	C/T	2.06699e-05	0.00321474	intron-variant	RNF19B	GRCh38.p7	1:32946612	CATTACAAATACAGC[C/T]AGTATTATCATAGGG	127544
rs780940031	snp	C/T			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933292	CGGAGTCTCGCTCTG[C/T]TGCCCAGGCTGGAGT	127544
rs780996707	in-del	-/C			intron-variant	RNF19B	GRCh38.p7	1:32942889	CTCACGCCTGTACTT[-/C]CAGCACTTTGGGAGG	127544
rs781163648	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32935126	TGAACCACTGCGCCC[A/G]GCCCATTATTTTATT	127544
rs781171201	snp	A/C			upstream-variant-2KB	RNF19B	GRCh38.p7	1:32965970	GCCGCTGCACCTAGC[A/C]AGAAATTTCTCTCTT	127544
rs781213355	in-del	-/T			intron-variant	RNF19B	GRCh38.p7	1:32951959	GCCACCACGCCCGGC[-/T]TTTTTTTTTTTTTTT	127544
rs781270912	snp	A/G	1.6755e-05	0.00289435	intron-variant	RNF19B	GRCh38.p7	1:32938567	GTTAATATGAGACCT[A/G]GGTATTCCAAGACAG	127544
rs781356399	snp	A/G	0.000115493	0.00759825	synonymous-codon	RNF19B	GRCh38.p7	1:32948359	TGGGCATGGCTTGAT[A/G]TCATCTGCTATGAGT	127544
rs781373793	snp	C/T			downstream-variant-500B	RNF19B	GRCh38.p7	1:32932218	CTACCTCTGCCACCA[C/T]AGGGGAGATGAGCAA	127544
rs781381230	snp	G/T			intron-variant	RNF19B	GRCh38.p7	1:32947638	CACTCCAGCCTGGGC[G/T]ACAGAGAGAAACTCT	127544
rs781386050	snp	A/G	1.82058e-05	0.00301705	utr-variant-3-prime	RNF19B	GRCh38.p7	1:32936774	GATGCAGTTACAAGT[A/G]TGCTTCTCAGAACAG	127544
rs781441186	snp	A/G	1.69726e-05	0.00291308	utr-variant-3-prime, synonymous-codon	RNF19B	GRCh38.p7	1:32936869	GGCTAGGGCAGAGAG[A/G]TTCATATGGGCACTT	127544
rs781457155	snp	C/G			intron-variant	RNF19B	GRCh38.p7	1:32944294	TCCCAAAAAGGTGGC[C/G]TGGTGTAACAGAATG	127544
rs781475735	snp	A/T	1.72973e-05	0.00294081	intron-variant	RNF19B	GRCh38.p7	1:32942490	AACATCCAATTCAAG[A/T]CAGCAGAGCATCAAA	127544
rs781497813	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32963440	CCCCACCTTGGCCGG[A/G]AGCGGTGGCTCACGC	127544
rs781621500	in-del	-/CAAG	1.64743e-05	0.00287	frameshift-variant, intron-variant	RNF19B	GRCh38.p7	1:32938469	TGTCACTAATTGCAC[-/CAAG]CAAGACTGGCTGTGT	127544
rs781711792	snp	C/T	0.00011698	0.00764697	missense	RNF19B	GRCh38.p7	1:32964117	CGGCGCAGCATGAAC[C/T]CCTCGTACTTGTGCA	127544
rs781766487	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32939619	TCCAGGGAATGAGAC[C/T]GAAGGACATACAGGA	127544
rs796144103	in-del	-/A			intron-variant	RNF19B	GRCh38.p7	1:32959901	AAAAAAAAAAAAAAA[-/A]TTAACCAGGCGTGGT	127544
rs796541649	in-del	-/TG			utr-variant-3-prime	RNF19B	GRCh38.p7	1:32933270	TTATTTTTTTTTTTT[-/TG]TGAGACGGAGTCTCG	127544
rs796741047	snp	C/T			intron-variant	RNF19B	GRCh38.p7	1:32942764	CTTTCCACTACACTG[C/T]TGCTTCCATGTAACC	127544
rs797009964	snp	A/G			intron-variant	RNF19B	GRCh38.p7	1:32962112	TAGCTGGGACTACAG[A/G]TGTGCACCACCATGC	127544

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