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

RNF212B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs142356564	snp	A/G	0.00676609	0.0577691	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184176	TCTTTTAGCGTAATT[A/G]TGAGCTACGAAGAGT	100507650
rs142365479	snp	C/T	0.00993419	0.0697739	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198764	TTAATAGTTCTCAAA[C/T]GGCTTTACATATGTA	100507650
rs142416211	in-del	-/GGCAGTGGTG	0.424193	0.179323	intron-variant	RNF212B	GRCh38.p7	14:23217247	AGTGGTGGCAGTGGT[-/GGCAGTGGTG]GGGGGGGGGCTCCTC	100507650
rs142432992	snp	C/T	0.00874735	0.0655527	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201236	TATCAGAAATCTGCA[C/T]TCAAGAGCACCTGTT	100507650
rs142475427	in-del	-/T/TT/TTT	0.480138	0.239828	intron-variant	RNF212B	GRCh38.p7	14:23227223	ATTTTATTATTATAA[-/T/TT/TTT]TTTTTTTTTTGGTAA	100507650
rs142538523	snp	C/T	0.00835141	0.0640778	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198086	TGGATCTTCAGTTAC[C/T]TCAGGCCATCTGGAT	100507650
rs142562760	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199721	GGAAGGGAGAAAAAA[A/C]AACAACAAACAAAAG	100507650
rs142594328	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260584	GAGCTTAGTTATCTC[A/G]CAAGTAAGACTGAAG	100507650
rs142639610	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23230018	GTTGTACCTGATTTT[A/G]TTATCAGTTTTCATC	100507650
rs142653077	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23263729	CTTCGGAGACTTTCT[A/G]TTAGTGACATGTGCC	100507650
rs142655084	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201224	AATCTCCAAAGCTAT[C/G]AGAAATCTGCACTCA	100507650
rs142658399	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253545	GCGGGGAAAGGTGAG[A/G]CAAGACCACTTTATT	100507650
rs142675675	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197225	TATCATCCAGAAAGG[A/G]TGAGAAAAATATAAC	100507650
rs142676281	snp	C/T	0.00914312	0.0669923	intron-variant	RNF212B	GRCh38.p7	14:23233106	TGATCTATGACCTTA[C/T]CCCCAACTCTGTGCT	100507650
rs142720335	snp	G/T	0.0189856	0.0955633	intron-variant	RNF212B	GRCh38.p7	14:23242061	CACTCCAGCCTGGGC[G/T]ACAGAGCAAGACTCC	100507650
rs142737404	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23239312	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	100507650
rs142757254	snp	C/T	0.0103295	0.0711199	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204899	TATGATTTCTCTCAG[C/T]AGTGTTTTGTACTTT	100507650
rs142799282	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23267310	ATTGTCTTATTTTCT[C/T]TTCAATTCTATCAGT	100507650
rs142892649	snp	C/T	0.0858192	0.188533	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212655	GGCGCAGTCTCGGCT[C/T]ACTGCAAGCTCCGCC	100507650
rs142926754	snp	C/T	0.0197687	0.0974348	intron-variant	RNF212B	GRCh38.p7	14:23263413	ATCTAGAAATGGAAC[C/T]ACTGCTCTTTTGACA	100507650
rs142932598	snp	C/G	0.00318978	0.0398085	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211919	TTTTAGTAGAGACAG[C/G]GTTTTGCCATGTTGG	100507650
rs142973527	snp	A/G/T	0.00319098	0.0398384	intron-variant	RNF212B	GRCh38.p7	14:23222969	TGAGGCAGGAGAATC[A/G/T]CTTGAACCTGGGAGG	100507650
rs143037205	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23269456	TACTGTATTTTGGCC[C/T]GGTAGTGGCTCCCAC	100507650
rs143142369	snp	A/G	0.0119091	0.0762411	intron-variant	RNF212B	GRCh38.p7	14:23238700	CCCTGATCTGCCACT[A/G]CACTCCAACCTGGAG	100507650
rs143143305	snp	A/G	0.0111196	0.0737302	intron-variant	RNF212B	GRCh38.p7	14:23264754	TTCTATGCATAATAT[A/G]ATGCCATTTCACTTG	100507650
rs143146142	snp	G/T	0.15665	0.231917	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197457	GCTTGAACCCGGGAG[G/T]CGGAGGTTGCAGTGA	100507650
rs143149950	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23219365	TAATAAAAAATAACA[A/G]CAACAGCTTTTTAAG	100507650
rs143176233	snp	C/T	0.00389672	0.0439679	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23258587	AACAGATCTCCTCAT[C/T]GCCTTTTATAAGCAT	100507650
rs143223586	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270020	ACACATATACTAAAA[C/T]GAAGATTTTCAAGAT	100507650
rs143285344	snp	G/T	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23229301	ACTAATGGACATTTG[G/T]GTTGTTTCTATCTTT	100507650
rs143313842	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195399	AAATGGAATTATAAG[C/T]GCTTGACTCGTAGCC	100507650
rs143319865	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23255398	CCATGATATCCTTAC[C/T]TGGTCCTAGTATGGA	100507650
rs143388124	snp	C/G	0.039522	0.134904	intron-variant	RNF212B	GRCh38.p7	14:23222610	AAGTAGAGGAGGAGG[C/G]AATACTTCCAAACTC	100507650
rs143396495	snp	A/C	0.254944	0.249951	intron-variant	RNF212B	GRCh38.p7	14:23238777	AATAATAATAATAAT[A/C]ATAATCCCACAAAGA	100507650
rs143406746	snp	A/G	0.0174175	0.0916809	intron-variant	RNF212B	GRCh38.p7	14:23191800	TCTTCACCATTATTT[A/G]CCTAAGGCCTAGAGC	100507650
rs143446814	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235877	ATAATTTTAATGTAA[C/G]CGGCTATAAAAAGTT	100507650
rs143493087	snp	G/T	0.0178098	0.0926698	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273517	AATGGTGGAATGGGC[G/T]AACAACACTATCACT	100507650
rs143521146	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246618	AACAAAAAACAGAGA[A/C]AGTCTTGCTATATTG	100507650
rs143523221	snp	C/T	0.00953873	0.0683987	intron-variant	RNF212B	GRCh38.p7	14:23186895	TCAGGATGCTATAGC[C/T]ACTGGTCAAAGCCTC	100507650
rs143569292	snp	A/G	0.0640965	0.167152	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210540	CCCAGAACTTTGGGA[A/G]GCTGAGGCGGGTGGA	100507650
rs143598665	snp	C/T	0.00318978	0.0398085	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274718	CAAGACCATCCTGGC[C/T]AACATGATGAAACCC	100507650
rs143689835	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199570	GAAGGCATTTTACAA[G/T]AAAATGAATCTCTGG	100507650
rs143884540	snp	C/G	0.0256215	0.110247	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204815	ATGGGGATTGTGTAT[C/G]GTCATTTTCACAATA	100507650
rs143918327	snp	C/T	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23192582	AGGAGATATACCTAA[C/T]GTGAATGACGAGTTA	100507650
rs143930821	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23252312	TGAGGAACCAGGGGC[A/G]AAGACCATATATGTA	100507650
rs143977155	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237025	TTGGAGTGCAGTGGC[A/G]TGAACACAGCTAACT	100507650
rs143981703	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225285	AGAGCTACCACATGA[A/T]CCAGCAATCCCACTA	100507650
rs144023440	snp	A/C	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259404	AGTCTCTGCATATTG[A/C]CCAGGCTGGTCTGGA	100507650
rs144069667	snp	C/T	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23220685	AGAAAATTAGCTGGG[C/T]GTGGTGGCGGGCACC	100507650
rs144136078	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23194563	GGCAACATGGTGAAA[C/T]TGCATCTCTACTAAA	100507650
rs144140637	snp	A/C	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23258263	GAATAGCTTGAACCC[A/C]GGAGGCAGAGGTTAC	100507650
rs144209502	snp	A/C	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23240889	AAGCAGTTTCATATC[A/C]ACCAATTTTATGTAA	100507650
rs144247068	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184081	AACGTTGAAAGGACA[C/T]CATCTTCGAGTTTCC	100507650
rs144277438	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203232	ATCAGTGAGAACATA[C/T]GATGTTTGGTTTTCC	100507650
rs144321036	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23238158	GGGTCGCCTTAATCA[C/T]CCTGTTCACTGCCTT	100507650
rs144475755	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246060	CTGTTTTGAATTCTT[C/T]ACTCACCTCAAGATA	100507650
rs144598555	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202773	GGAGAATGGCGTGAA[C/T]CTGGGAGGTGGAGGT	100507650
rs144634944	snp	A/G	0.00438332	0.0466095	intron-variant	RNF212B	GRCh38.p7	14:23191312	TAGTGAGCCGAGATC[A/G]CACTGCACCCTGGGC	100507650
rs144643802	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23194461	CTGATAAATCAGCCA[C/G]GCGCAGTGACACACA	100507650
rs144656288	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23248368	AACCCCTGGGCTCAC[A/G]CAATCTGCCCGCCTC	100507650
rs144659680	snp	A/G	0.00914312	0.0669923	intron-variant	RNF212B	GRCh38.p7	14:23250352	AGGTGTCATGGTGGC[A/G]CGTGCCTGTAATGCC	100507650
rs144695713	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215988	TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	100507650
rs144725519	in-del	-/AC			intron-variant	RNF212B	GRCh38.p7	14:23238419	TATCCCTCAGCGGTT[-/AC]ACACACACACACACA	100507650
rs144766756	snp	C/G	0.0189856	0.0955633	intron-variant	RNF212B	GRCh38.p7	14:23243650	GCAGTGAGCTGAGCT[C/G]GCGCCACTGCACTCC	100507650
rs144787145	snp	A/G	0.031825	0.122064	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209273	GCCGGTTCCTTTACC[A/G]CAACCTGTTTTACCA	100507650
rs144798060	snp	C/G	0.00874735	0.0655527	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202208	GTGAGCCGAGATTGC[C/G]CAACTGCACTCTAGC	100507650
rs144837758	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230984	GGTCTATATATGTCT[A/G]TCCTTATGCTAGAAA	100507650
rs144879444	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249864	CTTTTTTCCTCAAAT[C/G]TGTTCCCTCTGAACC	100507650
rs144916941	snp	A/T	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23235310	AGCTATGATTGTGCC[A/T]CTAAACTCTAGCCTG	100507650
rs144974520	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23267155	TTTATTTCAATTTTC[A/G]TGTCTTTGTAGAGAC	100507650
rs145005729	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210974	AAAGCAACAAATTCA[C/T]TTTGGGAGGCCAAGG	100507650
rs145031924	snp	C/T	0.00874735	0.0655527	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203844	TAGTTTACATTACCA[C/T]CAGTAGTGTAGAAGT	100507650
rs145080913	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23233914	CCAGCCTGGCCAACA[C/T]GGTGAAACCCTGTCT	100507650
rs145110717	snp	C/T	0.00874735	0.0655527	intron-variant	RNF212B	GRCh38.p7	14:23256369	TATTCTGCTTCTCCA[C/T]TGTTTAATTTTTTTT	100507650
rs145120206	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213558	ATCAGCAAATCACTG[A/C]AGAGAGCTAAACTTC	100507650
rs145145517	in-del	-/TA			intron-variant	RNF212B	GRCh38.p7	14:23240093	ATGTGTGTTTATATG[-/TA]TATATATATATACAC	100507650
rs145185025	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23251517	TTACCAGTTTATTAT[A/G]AAAGATACAACATAG	100507650
rs145213380	snp	C/T	0.0513262	0.151752	intron-variant	RNF212B	GRCh38.p7	14:23271090	CTATGATTCTGATTC[C/T]AGCAACAAAAGGTAA	100507650
rs145217081	snp	A/C	0.00318978	0.0398085	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184865	AAAACAGCATGAAGC[A/C]ATATAGTGGACAACA	100507650
rs145305768	snp	A/C/T	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23216562	AACAAATAAATTATG[A/C/T]TAAGTAAAAAAAAAA	100507650
rs145320562	snp	C/T	0.0298908	0.118541	intron-variant	RNF212B	GRCh38.p7	14:23216162	GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGC	100507650
rs145321930	snp	C/T	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23221850	ATTTTGGAAAGTATA[C/T]GAACACATGGAAATT	100507650
rs145337832	in-del	-/AA			intron-variant	RNF212B	GRCh38.p7	14:23225080	TTGATGCCACCCCAC[-/AA]ACAAAAAAAAAACAC	100507650
rs145395706	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212B	GRCh38.p7	14:23234450	ATTTTCGTCTGGTAC[C/T]TGTCTGTTTAGATTT	100507650
rs145401386	snp	A/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260556	GTCTTAGCAACCATG[A/T]CTAAGGGGCACTGAG	100507650
rs145420494	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189363	CTATGTATCTCCCCT[A/G]TTTGTGCACTAGCTT	100507650
rs145441464	snp	C/T	0.029116	0.117091	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197458	CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG	100507650
rs145461052	in-del	-/AT	0.0158469	0.0875917	intron-variant	RNF212B	GRCh38.p7	14:23190671	TCTCCCAATTTCCAC[-/AT]GTTTCTCCTACAAAT	100507650
rs145535510	snp	C/T	0.00953873	0.0683987	intron-variant	RNF212B	GRCh38.p7	14:23265063	TGACCTCAGGTGATC[C/T]GCCTTCCTCGGCCTC	100507650
rs145538668	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200981	TACAGAGAAACAAAT[A/G]TGCTCCAAATTTTGT	100507650
rs145601493	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23268340	CCTGTTGGTTTTCAA[A/G]GCTATCATGGAGGTG	100507650
rs145671078	snp	C/T	0.0256215	0.110247	intron-variant	RNF212B	GRCh38.p7	14:23235176	GAGATGGTGCCACTG[C/T]GCTCCAGCCTGGGTG	100507650
rs145712263	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23234101	ATGTGTACGAAGGAA[C/T]ACTCAAAAAGCCCAG	100507650
rs145715741	snp	C/G	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237533	TAAATTTTCCTGTTT[C/G]CGATTTTACGCTATT	100507650
rs145792081	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23243029	AGATGGGTAGACGTA[C/T]GGTGTGAAAGCCCTA	100507650
rs145797478	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195532	TTCATTATAGTCTCA[C/T]TTCTATTCAGTAATT	100507650
rs145798553	snp	A/G	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23256396	TTTTTTTTTGAGATG[A/G]AGTCTCACTCTGTTG	100507650
rs145816494	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23187715	AACTCACAGTCCATG[C/T]GCTCACTCCATCCTT	100507650
rs145822477	snp	C/T	0.0103295	0.0711199	intron-variant	RNF212B	GRCh38.p7	14:23246757	TATTAGTTTAAAGAA[C/T]AATGTGGAAAAGTCA	100507650
rs145825210	in-del	-/AAG	0.0182019	0.0936463	intron-variant	RNF212B	GRCh38.p7	14:23228685	ACAAAACAAAAACAC[-/AAG]AAGAAGAAAGAACAA	100507650
rs145865491	snp	A/G	0.0154538	0.0865337	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203527	TCTGTCACCCACGCT[A/G]GAGTGCAATGGCACG	100507650
rs145900323	snp	A/C	0.258565	0.249853	intron-variant	RNF212B	GRCh38.p7	14:23238780	AATAATAATAATAAT[A/C]ATCCCACAAAGAAAC	100507650
rs145941417	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230126	AGACATGATGAGAAG[C/T]GGAGTCGAATACACA	100507650
rs146028724	snp	G/T	0.0150606	0.0854603	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197319	ATTTCATGAGGCCAT[G/T]AGTTTGAGACCAGCC	100507650
rs146040042	snp	C/G	0.0123036	0.0774623	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199731	AAAAACAACAACAAA[C/G]AAAAGAACATTCTTG	100507650
rs146050966	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241370	TGGAAGGCTCTATAC[A/G]CTGGGCTAAAGAGCC	100507650
rs146109473	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242108	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAA	100507650
rs146146945	snp	C/T	0.0197687	0.0974348	intron-variant	RNF212B	GRCh38.p7	14:23247062	GGAGAATCACTTGAA[C/T]CTGGGAGGTGGAGAC	100507650
rs146163307	snp	A/G	0.00993419	0.0697739	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212297	GCAGTTAGGCAAGAA[A/G]AAATAAAGGTATACA	100507650
rs146168753	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23258783	ATTTGTTTGTTTGGG[A/G]AAATCAGGTACAGAA	100507650
rs146187230	snp	A/C	0.0185938	0.0946107	intron-variant	RNF212B	GRCh38.p7	14:23262009	AACAAAACTCTCTCT[A/C]TATATACACACACAC	100507650
rs146222536	in-del	-/C	0.0803491	0.183626	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211296	GAAAGACATAAACTA[-/C]TAAAACACAGGCAAG	100507650
rs146268322	snp	A/G	0.0547245	0.156101	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211122	ACCTGGGAGGCTGAG[A/G]CAGGAGAATTGCTTG	100507650
rs146272426	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23224013	TATAAAATTAATTAC[C/T]GAGGAATTAACCAAA	100507650
rs146283718	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23229629	ATTTGCATTTCCCCT[A/G]TGACTAATTATATTG	100507650
rs146287932	snp	C/T	0.00159617	0.0282053	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274733	TAACATGATGAAACC[C/T]GTCTCTACTAAAAAT	100507650
rs146302602	snp	A/G	0.0368353	0.130617	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212501	ATCAATAACAGAAAA[A/G]TCAGTTGTACTTCTA	100507650
rs146396868	snp	A/G	0.00358779	0.0422022	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199020	ACTGAGAGGGCCTAG[A/G]GGCAATGACACCCCC	100507650
rs146413244	snp	G/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23225347	TATATCAAAGAGATA[G/T]CTGCACTCCCTTGTG	100507650
rs146417179	snp	C/G	0.0426489	0.139662	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260639	GCAGCTTTCTTCACT[C/G]CTGGTTTTTTCACCT	100507650
rs146424934	snp	C/T	0.00438332	0.0466095	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23195068	AAATTTGAAAATGAA[C/T]GAAATAACTCGGTTA	100507650
rs146447898	snp	C/T	0.0391387	0.134304	intron-variant	RNF212B	GRCh38.p7	14:23220693	AGCTGGGCGTGGTGG[C/T]GGGCACCTGTAGTCC	100507650
rs146499321	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23235177	AGATGGTGCCACTGC[A/G]CTCCAGCCTGGGTGA	100507650
rs146548925	snp	C/T	0.00716266	0.059414	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207281	AGACAGAATCCCAAA[C/T]CAGTTTCTTACCTAG	100507650
rs146571540	snp	C/G	0.0119091	0.0762411	intron-variant	RNF212B	GRCh38.p7	14:23238534	GGAGTTCCAGACCAG[C/G]CTGGGTAACACAGAG	100507650
rs146615253	snp	C/T	0.0111196	0.0737302	intron-variant	RNF212B	GRCh38.p7	14:23250353	GGTGTCATGGTGGCG[C/T]GTGCCTGTAATGCCA	100507650
rs146631696	snp	A/G	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23257345	ACATTTTCTTTTCAC[A/G]GCTTAAAATAAACAT	100507650
rs146647966	in-del	-/C	0.0197687	0.0974348	intron-variant	RNF212B	GRCh38.p7	14:23263975	CGCCTGTAGTCCTAG[-/C]TACTTGGGAGGCTGA	100507650
rs146688025	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195438	CCATATCTCTTGTCT[A/G]CCTCTAAGGCTTCGA	100507650
rs146692427	snp	A/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23255908	TGATATAGGCTAAAC[A/T]TTTGTACCCTGGCAT	100507650
rs146734366	snp	A/T	0.000399281	0.0141238	intron-variant, stop-gained	RNF212B	GRCh38.p7	14:23268062	TCTCCTTAGGCAGCC[A/T]AACAAGTGCTTCTAA	100507650
rs146757871	in-del	-/T	0.0314385	0.121371	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200030	TTAAAAAAAAAAAAA[-/T]TTAGGCAAGACTAGA	100507650
rs146809272	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208009	CAAAGGAGGCAATCA[A/G]ATATGCATCTATATC	100507650
rs146812417	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23272053	GAGAGTAGAAATAAA[A/G]GATTGGCCATTAATT	100507650
rs146877848	snp	A/G	0.212728	0.247206	intron-variant	RNF212B	GRCh38.p7	14:23271375	TTGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC	100507650
rs146920554	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273295	TGTCCCATTGCCAAT[A/G]TTAACGAGCAATATC	100507650
rs146935675	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211626	CAATGCATAAAAAGG[A/T]TAATACGTCATGAAC	100507650
rs146965230	snp	C/G	0.125528	0.21681	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209124	GATTATTCATGCCTC[C/G]CCTTTTTAGACCATA	100507650
rs147070698	snp	A/G	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23223011	GTGAGCCAAAATTGC[A/G]CCATTGAACTCCAGC	100507650
rs147103589	snp	C/G	0.00279162	0.0372561	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195961	CTCACTGCATTTGCT[C/G]TTTTCACTGTGCCAC	100507650
rs147165592	snp	G/T	0.031825	0.122064	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236697	TAGATGCAATTTACA[G/T]AAACAAAAGCTCTTT	100507650
rs147193385	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189481	ATTATTCCTGTCAGC[A/G]TACAGATGTGCTGTA	100507650
rs147247905	in-del	-/T	0.0376037	0.131863	intron-variant	RNF212B	GRCh38.p7	14:23258820	TCCCCTGAATCTCCA[-/T]TTTTTTCTCTTTCTT	100507650
rs147252098	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23247140	AGCAAAACTCCATCT[A/C]AAAAAAAAAAAAAAT	100507650
rs147266144	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252657	GGTGTGGGGATCATT[A/G]ATTGGTTAAGGAATG	100507650
rs147269668	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23193574	CTGGAACATAGTACC[C/T]AGGGGGCGGATTTAT	100507650
rs147300120	snp	C/G	0.00279162	0.0372561	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203269	GGGCTACTTCACTTA[C/G]AATAATAGTCTCCAA	100507650
rs147309044	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23266752	CCTAACATGTGGTCT[A/G]TCCTGGAGAATGCTC	100507650
rs147376821	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204949	GGACTTTAAAAGCAC[A/G]TATAGAAAGATACAT	100507650
rs147378366	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23269646	GAGTTTAGGAAGTCA[A/C]GGCTGCAGTGAGCCA	100507650
rs147393179	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253288	CCACATTTTGAATTG[A/T]GTTTCAATAAAGGTA	100507650
rs147406616	snp	A/G	0.0295035	0.117819	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23216028	AGGCGGGCGGATCAC[A/G]AGATCAGGAGATCGA	100507650
rs147482119	snp	A/C	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23219534	TGGAGTGCAGTGGCA[A/C]GATCTCGGCTCACTG	100507650
rs147497295	snp	A/G			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270371	ATAGCTCACCTAAAT[A/G]TTTATATTGGCTATT	100507650
rs147512610	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234051	GCAGTGAGCTGAGAT[A/G]GTACCACTGCACTTG	100507650
rs147514513	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274212	TAATTCACTTAAAGA[C/T]GATGGTCCCTCTGTC	100507650
rs147605820	snp	C/G	0.00676609	0.0577691	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184967	GGCCTAAAAAATTAA[C/G]TTCCCCCAAACTGAC	100507650
rs147607813	snp	A/G	0.0166325	0.0896639	intron-variant	RNF212B	GRCh38.p7	14:23245241	GTGTCCTGCCTCTCA[A/G]TCCTCACTCTAGAGA	100507650
rs147677939	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23232175	GGGCCTCTTCCCCGC[C/T]GCCATCCCGTCTAAG	100507650
rs147688803	in-del	-/TCT			intron-variant	RNF212B	GRCh38.p7	14:23191466	TTTGTTCCTTGTTTG[-/TCT]TTCCTATTAAAATGT	100507650
rs147739962	snp	C/G	0.0475351	0.146656	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198601	GAATCACTTGAACCT[C/G]GGAAGCAGAGGTTGC	100507650
rs147782761	snp	C/T	0.0119091	0.0762411	intron-variant	RNF212B	GRCh38.p7	14:23246237	CCTCCAGGGTTCAAG[C/T]GATTCTCCTGGGGGC	100507650
rs147815814	snp	C/G	0.0283406	0.115616	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213108	ACAAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT	100507650
rs147845323	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211275	ATAAAAATGGACGAA[C/T]TCCTTGAAAGACATA	100507650
rs147848715	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23248804	CTTCATGACATAATC[A/G]CCTCCTAAAGCCTCC	100507650
rs147863352	in-del	-/TTTG	0.250234	0.250889	intron-variant	RNF212B	GRCh38.p7	14:23227607	AACAAAAAGTGTTTT[-/TTTG]TTTTGTTTGTTTTGA	100507650
rs147916079	in-del	-/AAAC	0.261608	0.24973	intron-variant	RNF212B	GRCh38.p7	14:23254289	TACTCTTTATCTCAA[-/AAAC]AAAACAAAACAAAAC	100507650
rs147922305	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231193	CATTGAATCCGTATA[C/T]AGCTTTGGATGCTAT	100507650
rs147952111	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23227060	AGTAATGTCATGAGG[A/T]CTATGGATGGTACCA	100507650
rs147954609	snp	C/G	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23267157	TATTTCAATTTTCAT[C/G]TCTTTGTAGAGACGA	100507650
rs147970072	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23235920	TCAGATCCCACTTTG[C/G]AATCAACTTTTAACT	100507650
rs148010903	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23246694	TGCCCTACCAAAGTG[C/T]CAGGATTACAGGTGT	100507650
rs148101798	snp	C/T	0.00755907	0.0610114	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270254	ATTGAAAATGCTGGG[C/T]GCTCAGTTCTGAGGA	100507650
rs148135885	snp	C/T	0.00279162	0.0372561	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274629	AGAACTGAAAATAGC[C/T]GGGCACGGTGGCTCA	100507650
rs148141287	in-del	-/TGTG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196379	GTCACCACTGCTCTC[-/TGTG]CCACAGCCACACCAA	100507650
rs148190299	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23269481	TCCCACCTGTAATCC[C/T]AGCACTTCGGGAGGC	100507650
rs148215778	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213299	GCCTGGGCGACAGAG[C/T]AAGACTCCGTCTTAA	100507650
rs148259087	snp	A/C	0.00795532	0.062565	intron-variant	RNF212B	GRCh38.p7	14:23229372	CATATCTGTTTGAGC[A/C]CCTGTTTTAAATTAT	100507650
rs148321171	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196366	AAGCCCACTCTGCGT[A/C]ACCACTGCTCTCTGT	100507650
rs148327967	in-del	-/CA			intron-variant	RNF212B	GRCh38.p7	14:23240007	AACACACACACACAC[-/CA]ACACACACACTCATA	100507650
rs148386923	in-del	-/AAC	0.159622	0.233092	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206945	GTCTTAGAAGAGAAA[-/AAC]AACAACAACAAACAA	100507650
rs148447175	in-del	-/AAAC	0.474182	0.110646	intron-variant	RNF212B	GRCh38.p7	14:23261968	TGGGACTCTGTCTCA[-/AAAC]AAACAAACAAAAAAA	100507650
rs148488208	snp	C/T	0.00993419	0.0697739	intron-variant	RNF212B	GRCh38.p7	14:23253476	TTCCTCTGTCCTCTA[C/T]TTCTTGTAAATTGTT	100507650
rs148497816	snp	A/G	0.0858192	0.188533	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212643	CTGGAGTGCAGTGGC[A/G]CAGTCTCGGCTCACT	100507650
rs148548687	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209919	GCACTTTGGGAGGCC[A/G]AGGTGGGCTGATCAC	100507650
rs148569802	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23263341	CAACTTTTCACAAGC[C/T]AACCCTGACTTTCAG	100507650
rs148575732	snp	C/T	0.00636936	0.0560724	intron-variant	RNF212B	GRCh38.p7	14:23267245	CCTCAGCTCCCAAAG[C/T]GCTGGGATTATAGGC	100507650
rs148705384	snp	A/C	0.00795532	0.062565	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184082	ACGTTGAAAGGACAT[A/C]ATCTTCGAGTTTCCT	100507650
rs148711173	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23271214	GAGGCCGAGGCAGGT[A/G]GATAACCTGAGGTCA	100507650
rs148748661	snp	C/T	0.0298908	0.118541	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215983	GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	100507650
rs148760162	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23239785	CACCATGCCCAGCTA[A/G]TTTTTATATTTTTAG	100507650
rs148817404	snp	A/G	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23246259	CCTGGGGGCAGGGCA[A/G]TTTCAATCTTACTCA	100507650
rs148821950	snp	C/T	0.0115144	0.0749975	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273277	TTTTAGCTTTGGATA[C/T]ACTGTCCCATTGCCA	100507650
rs148936939	snp	C/T	0.0154538	0.0865337	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203541	TGGAGTGCAATGGCA[C/T]GATCTTGGCTCACTG	100507650
rs148946584	snp	A/G	0.221439	0.248363	intron-variant	RNF212B	GRCh38.p7	14:23232774	CCAGCCGCCCCGTCT[A/G]GGAGGGAGGTGGGGG	100507650
rs149007814	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195845	TTCAAGGTAAACGTT[A/G]TTTTGCATTTTACAA	100507650
rs149063961	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249915	TTACAAATCTGAACA[A/G]GTAACTGCCTTTTCA	100507650
rs149083474	snp	C/T	0.00318978	0.0398085	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211070	TGAAAATAAAAAAAT[C/T]AGCTGGTCGTGATGG	100507650
rs149097571	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23238761	TAATAATAATAATAA[C/T]AATAATAATAATAAT	100507650
rs149152481	snp	C/T	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23264723	ACTCTATGCGAAGAT[C/T]TGCGGATTTCTGGTT	100507650
rs149189565	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23191705	TAAGTGGGATGATGG[A/G]TAATAGTCCATTAGA	100507650
rs149219959	snp	A/G	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23222014	GGGAAATGTATAGCT[A/G]TAAGTGTCTACATCA	100507650
rs149243594	in-del	-/CACACA			intron-variant	RNF212B	GRCh38.p7	14:23257150	AGAGCGAGACTCAGT[-/CACACA]CACACAAAAAAAATA	100507650
rs149262912	snp	A/G	0.0185938	0.0946107	intron-variant	RNF212B	GRCh38.p7	14:23266693	TGAGATTACAGGCGT[A/G]AGCCACCACACCCGG	100507650
rs149293083	in-del	-/C	0.0123036	0.0774623	intron-variant	RNF212B	GRCh38.p7	14:23254592	AGAGATAGCATTTTG[-/C]CACGTTGCCCAGGCT	100507650
rs149298511	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260527	TACTGCTGCTACTTT[C/T]CCTCCTACTGGGAGT	100507650
rs149316095	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23235590	CTTTCAGATGAAAAT[C/T]AGACCTTTGGAAAAC	100507650
rs149344086	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189239	GAAAATGGGAATAGG[A/C]AGAAGAGAACTTCCC	100507650
rs149348041	snp	A/G/T	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23247792	TGGGTATATACCTAC[A/G/T]AGTGGAATTTCTGGG	100507650
rs149486751	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23219477	TTCTTCTCCTTCTAG[-/T]GTTTTTTTTTTTTTT	100507650
rs149505783	snp	C/T	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23219620	GGAATGATAGGCGTG[C/T]ACCACCATGCCCAGC	100507650
rs149523533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23268765	TATAAGAGATACTGC[C/T]ATGTGATTTGTGAGC	100507650
rs149713765	snp	C/T	0.122758	0.215196	intron-variant	RNF212B	GRCh38.p7	14:23194065	CAGGCTGGTCTGGAA[C/T]TCCTGACCTCAGGTG	100507650
rs149732841	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23186418	TGCGATCTCGGCTCT[C/T]GGCTCACTGCAACCT	100507650
rs149787341	snp	A/G	0.00636936	0.0560724	intron-variant	RNF212B	GRCh38.p7	14:23241519	ACCTCTGCTTCCCAG[A/G]TTCAAGCGATTCTCA	100507650
rs149787572	in-del	-/CT/CTCTCTAAAAAAAC/CTCTCTCT	0.0569648	0.160495	intron-variant	RNF212B	GRCh38.p7	14:23228639	GGTGACAGAGCAAGA[-/CT/CTCTCTAAAAAAAC/CTCTCTCT]CTCTCTAAAAAAACA	100507650
rs149839803	snp	C/T	0.00716266	0.059414	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237512	GTTCTTTGTCCGCAT[C/T]ATTTTTAAATTTTCC	100507650
rs149874264	snp	C/G	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23190192	CCTCCCTCTCTAGCT[C/G]TGTGATGTCATCCAG	100507650
rs149879870	snp	C/T	0.030278	0.119257	intron-variant	RNF212B	GRCh38.p7	14:23249190	ACTGTTGGAATAAAA[C/T]CAGGTCAAGATTTGA	100507650
rs149911887	snp	A/T	0.00108926	0.0233119	missense, nc-transcript-variant	RNF212B	GRCh38.p7	14:23262959	TTTCCAGCATAGCAG[A/T]CAAGTGGTCAGGTAA	100507650
rs149915401	snp	C/T	0.0349115	0.127424	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200514	TAATTTCAGCAGAGA[C/T]GGGGTTTCACCATGT	100507650
rs150049144	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206273	AGATACAGGGTTTCA[C/T]CACGTTGGCCAGGCT	100507650
rs150052705	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23271044	TACTTCTCCAGAGAC[C/T]GCTAGAATAATATTT	100507650
rs150106257	in-del	-/G	0.149999	0.229128	intron-variant	RNF212B	GRCh38.p7	14:23252091	TGATTGTCAGGGGTT[-/G]GGGGGGCGTGGGAAG	100507650
rs150161951	snp	C/T	0.000317712	0.0125998	stop-lost, utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272889	TGGACCACTTCTAGA[C/T]AGATCATCTTCAAGA	100507650
rs150176457	snp	A/C			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23235907	TCATTGATATGGTTC[A/C]GATCCCACTTTGCAA	100507650
rs150215034	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23267924	TCTGCCAGTTTCTGC[A/C]TTTTAATTCATTTAC	100507650
rs150248689	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195525	CTCTTCCTTCATTAT[A/G]GTCTCATTTCTATTC	100507650
rs150294319	snp	A/G	0.151668	0.229849	intron-variant	RNF212B	GRCh38.p7	14:23243736	CAAGCAAGCAAGCAA[A/G]CAAGCAAGCAAAGAA	100507650
rs150373652	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23238771	AATAATAATAATAAT[A/C]ATAATAATAATCCCA	100507650
rs150440309	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23263996	GGGAGGCTGAGGCAT[A/G]AGAATCACTTGAACC	100507650
rs150442235	snp	A/G	0.00755907	0.0610114	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201847	CCTAATAAAAACAGC[A/G]TGGAGCCAATTCCAC	100507650
rs150460838	snp	A/G	0.0103295	0.0711199	intron-variant	RNF212B	GRCh38.p7	14:23221316	AGATGTGCCATGACA[A/G]TGGAAACCAAAAAAG	100507650
rs150498084	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23266299	TTGTTTTTTGGACCC[A/G]TTGGTTGTTTATCAA	100507650
rs150545360	snp	A/G	0.00597247	0.0543191	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203032	AGTATTTGGTTACAT[A/G]ACTGAGTTCTTTAGT	100507650
rs150640802	snp	A/C	0.00795532	0.062565	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212900	ACAATTTTTTGAAGT[A/C]ATTTCTTTTTTGCCA	100507650
rs150682878	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23188768	AACCACTGTGCTGGG[C/T]CTCAGGTTTTTAAAG	100507650
rs150691699	snp	C/T	0.00835141	0.0640778	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274645	GGGCACGGTGGCTCA[C/T]GCCTATAATCCCAGC	100507650
rs150709377	snp	C/T	0.0162398	0.0886349	intron-variant	RNF212B	GRCh38.p7	14:23233845	CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAAG	100507650
rs150719058	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200440	AAGCAATTCTCATGC[C/T]TCAGCTTCCCAAGTA	100507650
rs150776318	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258067	AAAGGGGCCGGGTGC[A/G]GTGGCTCACGCCTGT	100507650
rs150777525	snp	A/C	0.0023933	0.0345097	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196824	TTCACTGCTATTCAT[A/C]CTTCTGATTTAGCAC	100507650
rs150845246	snp	C/T	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23244743	TATATAGGCCTGGCC[C/T]TGCAAACAATAGGTT	100507650
rs150902568	snp	A/C	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214827	AAATAATGGCTGAAA[A/C]CTTTCCAAATCTGTT	100507650
rs150940773	snp	C/T	0.0111196	0.0737302	intron-variant	RNF212B	GRCh38.p7	14:23253765	TATCCAGATATATAG[C/T]TCAAAAATACTAAGA	100507650
rs151003742	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23216178	GTGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGT	100507650
rs151029188	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23267573	AGCTGGGATTATAGG[C/T]ATGTGCCACCACGCC	100507650
rs151083084	snp	A/G	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23263576	AGAGGACATAAAAAC[A/G]AATTTGTTTTTTCAT	100507650
rs151100027	snp	C/T	0.0142736	0.0832652	intron-variant	RNF212B	GRCh38.p7	14:23226166	AGCAGGGTGTGGTGG[C/T]GGGTGCCTGTAATCC	100507650
rs151221630	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23189840	GAACAGAACTTCCCT[G/T]GATGCTCTATTCCTT	100507650
rs151241141	snp	A/G	0.00953873	0.0683987	intron-variant	RNF212B	GRCh38.p7	14:23235083	CAGGCGTGGTGGCAA[A/G]TGCCTGTAATCCCAG	100507650
rs151251283	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201405	CACAGTAATTTTAAC[G/T]TAACATAACAATTAT	100507650
rs151272933	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184217	CAAAATCGCCAGGCG[A/C]GGTGGCTCACGCCTG	100507650
rs151302687	snp	A/G	0.0154538	0.0865337	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198128	AGTCACAGGGGATGC[A/G]ATGGCCTGGCCTGGG	100507650
rs151308758	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259432	GGAATCCTTTTTTTT[A/T]CTTCTTTTAAAGTTT	100507650
rs180674233	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200234	TTGATGAAACTTTGT[C/T]CCATAGGAGGAATCT	100507650
rs180678936	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23233634	GTAGTCCCAGCCACT[C/T]GGGAGGCTGAGTTAG	100507650
rs180691173	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222505	TAAAAAGTCTCCCAA[C/T]AAAGAAAAGCCTGAG	100507650
rs180698546	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244205	ATCTCCCTTTTACAC[A/G]CAGTGGAGATAATGT	100507650
rs180717913	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215441	ACCCAGGAATTTGAG[C/G]TTACAATGAGACATG	100507650
rs180718702	snp	A/C	0.0209421	0.100162	intron-variant	RNF212B	GRCh38.p7	14:23263753	ATGTGCCCCTTCCCC[A/C]AAAAAAAACGAGTGT	100507650
rs181064509	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187748	TCTCGTAACTATGTG[C/T]CCCATATCTATGTGC	100507650
rs181135350	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199853	TGTTTAGTCTCAGTT[A/C]GCTGGGCTTTAAGAA	100507650
rs181135527	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215169	TGATGGTTTAAAAGT[A/G]TTTGGCAGTTCCCCC	100507650
rs181153846	snp	C/T	0.00597247	0.0543191	intron-variant	RNF212B	GRCh38.p7	14:23243995	AGGCAGAAGAATCAC[C/T]TGAACCCAAAAGGCG	100507650
rs181166362	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263176	GGCAGACAATCATTA[A/G]CAGTATACAACAACT	100507650
rs181170384	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229132	CTCTTTTTGTGTCTG[A/G]CTTATTTCACTTAGC	100507650
rs181264269	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23222924	CCGGGCATGGTGGCA[C/T]GCACCTGTAATCCTA	100507650
rs181266623	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212210	AATGCTTTTTCCCTA[A/T]GATCAAGACTAACAC	100507650
rs181271960	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23234648	TTGATTCTGTTTCAT[C/T]GGTCTACACGTTTAT	100507650
rs181272216	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195568	TAGTGCTAATTCTCC[C/T]CTACTTCATGCACTC	100507650
rs181280049	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270365	TCTTCCATAGCTCAC[C/T]TAAATATTTATATTG	100507650
rs181288128	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189289	CTGTCAATCTACCTG[A/C]AGCTCTCCCCACATC	100507650
rs181293266	snp	A/G	0.0119091	0.0762411	intron-variant	RNF212B	GRCh38.p7	14:23258358	AAAAAAAAAAAAAAG[A/G]CAGTAGAAGGCTAGT	100507650
rs181293362	snp	A/G	0.0279526	0.114869	intron-variant	RNF212B	GRCh38.p7	14:23226276	CACTCTAGCCTGGGC[A/G]ACAGAGCAAGAAACC	100507650
rs181298634	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23238759	AATAATAATAATAAT[A/C]ATAATAATAATAATA	100507650
rs181349579	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247410	CAGGCACTTCCCAAA[C/T]CCTTCCCACCCTCCC	100507650
rs181355128	snp	A/G	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23218231	AAATTAGCCGGGCGT[A/G]GTGGCACACACCTGT	100507650
rs181370219	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23253803	GTAGATATTATGGAA[C/T]GAGGGAGTTTCACAA	100507650
rs181444553	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183630	CCGGCCCCATCCCTC[C/T]GGTTTCGGGAGAGTG	100507650
rs181448252	snp	A/G	0.0154538	0.0865337	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203609	TCAGCCTCTCAAGTA[A/G]CTGAGATTATAAGTG	100507650
rs181458827	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23219616	AGCTGGAATGATAGG[C/T]GTGCACCACCATGCC	100507650
rs181466478	snp	A/G	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23232202	TAAGAAGTGAGGAGC[A/G]TCTCTGCCCGGCTGC	100507650
rs181467527	snp	C/T	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23232067	GCCCGGCTGCCACCC[C/T]GTCTGGGATGTGAGG	100507650
rs181472389	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205393	ATAAAATACCTATTA[A/C/T]TGAATTTAACTTTAT	100507650
rs181477998	snp	C/G	0.0166325	0.0896639	intron-variant	RNF212B	GRCh38.p7	14:23225982	CCAAGTATGTACCCA[C/G]AAAAATGAAAAATTT	100507650
rs181490125	snp	A/G	0.00358779	0.0422022	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23195170	TTGTGGTGCACGTCT[A/G]CAGTCCCAGCTATTT	100507650
rs181497884	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248491	CTGTCGCCCAGACTG[C/G]AGTGCAGTGGCACGA	100507650
rs181501419	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272343	GAGAATGGCGTGAAC[C/T]CGGGAGGCGGAGCTT	100507650
rs181509662	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23257033	TGGCGGACGCCTGTA[A/G]TCCCAGCTACTCAGG	100507650
rs181608017	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211405	TCCAGGCTTAGATGG[A/C]TTCACTGGTAAGTTC	100507650
rs181638385	snp	A/G			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237382	TGATCCGCCCGCCTC[A/G]GCCTCCCAAGGTGCT	100507650
rs181901837	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204463	AGCCAATTATCCCAG[C/T]GCCATTTATTAAAAA	100507650
rs181982364	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23222823	TTTGGGAGGCTGAGG[C/T]GGGGGGATCATCTGA	100507650
rs181995413	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209331	GCTGACCTATCTCAT[C/T]CTGTGACTTAGAATG	100507650
rs181999837	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23252676	GGTTAAGGAATGCAG[A/G]TTGAAGTCATGAGAA	100507650
rs182009032	snp	A/C/G	0.0182019	0.0936463	intron-variant	RNF212B	GRCh38.p7	14:23233895	TGAGGTCAGGAGTTC[A/C/G]AGACCAGCCTGGCCA	100507650
rs182051665	snp	A/G	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23232158	ACTCTGGGAAGTGAG[A/G]AGGGCCTCTTCCCCG	100507650
rs182063436	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209978	GCCAACATGATGAAA[C/T]CCTGTCTCTGTTAAA	100507650
rs182080114	snp	C/T	0.00914312	0.0669923	intron-variant	RNF212B	GRCh38.p7	14:23190756	CAGATCAGGTCATGT[C/T]CCTCCCCTGTTCAAA	100507650
rs182082664	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23271775	CGTCTACAAATATAT[A/G]GCCCCTAATTGGATC	100507650
rs182095471	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23223424	GCAGTGATATGATCT[C/T]GGCTCACTGCAACCT	100507650
rs182102949	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235160	GAGGTTGCAGTGAGC[G/T]GAGATGGTGCCACTG	100507650
rs182171049	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267908	TTTTTCTTTCATCTG[C/T]TCTGCCAGTTTCTGC	100507650
rs182177771	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23188964	ATGACTCCTTGATAT[A/G]CCAACTAATTGTAGC	100507650
rs182212861	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259331	GTAGCTGGGACTACA[A/G]GTGCACACCACTATG	100507650
rs182218921	snp	A/G	0.0107246	0.0724382	intron-variant	RNF212B	GRCh38.p7	14:23232406	GATCCCCTCCGCCCG[A/G]CAGCCGCCCTGTCTG	100507650
rs182228282	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244846	TTTTCAATAACCTTT[A/T]TAGTAATACTTACCT	100507650
rs182364250	snp	A/G	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23219371	AAAATAACAACAACA[A/G]CTTTTTAAGACAAAG	100507650
rs182389700	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247581	ATGTTGTAGCATCTC[A/T]GTTAGGACTTTATTA	100507650
rs182439821	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254143	TTAAAAAATTAGAGG[A/G]GTATGGTGGCATGCA	100507650
rs182445286	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201982	GAGGCCGGGCACAGT[A/G]GCTCATGCCTGTAAT	100507650
rs182458551	snp	A/G	0.0640965	0.167152	intron-variant	RNF212B	GRCh38.p7	14:23230451	CGAGGTCAAGAGATC[A/G]AGACCATCCTGGCTA	100507650
rs182490799	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229515	CCCATCAGCAATGTA[C/T]AAGGGTTCTGATTTC	100507650
rs182516103	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265603	CTCCTTTGAAAAACA[C/T]AGATGTTCTAGCCAA	100507650
rs182598046	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204608	TATACCAGTACCATG[C/G]TGTTTTGGTGACTAT	100507650
rs182609308	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274013	ATTTGGTTCCATTAA[A/T]CCCTAAACCATAGGA	100507650
rs182666113	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230136	AGAAGCGGAGTCGAA[A/T]ACACACCACAATGGT	100507650
rs182673464	snp	A/G	0.0107246	0.0724382	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200789	GGCTTCTTAAGTCAA[A/G]TTTGATTCCTTATAG	100507650
rs182676432	snp	C/T	0.0295035	0.117819	intron-variant	RNF212B	GRCh38.p7	14:23216118	GAGTGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	100507650
rs182713827	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23246227	GCAACCTCTGCCTCC[A/T]GGGTTCAAGCGATTC	100507650
rs182787700	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250560	GTACTTGTGTTCTGC[A/G]TATAACCTAGTGTTT	100507650
rs182793070	snp	A/G	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23227869	CCCCCGAAGTGCTGG[A/G]ATTACAGGCTTGAGT	100507650
rs182803244	snp	C/T	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274635	GAAAATAGCCGGGCA[C/T]GGTGGCTCATGCCTA	100507650
rs182803623	snp	G/T	0.00279162	0.0372561	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198031	GGAACAAATCACAAT[G/T]GTGGAATGTCATCAG	100507650
rs182808365	snp	A/C	0.00398564	0.0444627	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213647	GTGTCAGTGGGACCC[A/C]GTGGGGAGCTGAACA	100507650
rs182811171	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23261472	GGAACCTCCACCTTA[C/T]TTTTTACACTACTCA	100507650
rs182818700	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240639	CTAAATTATTTAGCA[A/G]ATGATTTAGCAAATC	100507650
rs182873839	snp	A/C	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23249653	CAGTGTAGTTGAATT[A/C]TTCATCACTACTGAG	100507650
rs183051930	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23245850	GCTCCATGAAAACAG[A/G]TTTGGTTGGTTTTGC	100507650
rs183056868	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266880	TATGCTTCTGTTTCC[C/T]TTCCTTGCTGATCTT	100507650
rs183115332	snp	A/C	0.00597247	0.0543191	intron-variant	RNF212B	GRCh38.p7	14:23220712	CACCTGTAGTCCCAG[A/C]TACTCAGGAGGCTGA	100507650
rs183122611	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184769	AAATGATGCCTCCAC[C/T]TTCTTGAAGAATTTC	100507650
rs183128675	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23248913	GGCCAGTAAATATTT[C/T]AAGCTTTGCAGGCCA	100507650
rs183218627	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208283	TTCCAGCACATTGGA[C/T]GAGAAGATCACTGGA	100507650
rs183225234	snp	C/T	0.0256215	0.110247	intron-variant	RNF212B	GRCh38.p7	14:23221124	AGGCGCAGTGGCTCA[C/T]GCCTATAATCCCAGC	100507650
rs183255671	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197099	TATATAGGACATGTA[C/T]GTGGTAACACTTGGT	100507650
rs183292101	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23227241	TTTTTTTTGGTAAAA[C/T]GGAGTAGAAACTTTA	100507650
rs183314759	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259632	GTGTGTGGGTGGAGA[A/G]AGGAAATGGAATTCT	100507650
rs183386022	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207007	GCACACATACACACA[C/T]ACATCTTGGGTGTGT	100507650
rs183396587	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236071	TCCAACCAAAACAGC[A/G]TACTGCAAAAGTTAA	100507650
rs183405432	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23254727	AGAATGTTTTGTTTA[C/T]AATAACCCACATTGG	100507650
rs183406994	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23224068	AACTATAAAACATTG[A/G]TGAAAGAAATTGAGG	100507650
rs183407361	snp	A/G	0.256619	0.249912	intron-variant	RNF212B	GRCh38.p7	14:23232294	CCTCTGCCCGGCCGC[A/G]ACCCCATCTGGGAGG	100507650
rs183413502	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23272754	GCTTCATACAACAGG[C/T]CAGAGAGACTTGCTT	100507650
rs183435776	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236601	TGGGGTTTATTATTG[C/T]TTTCAAATAATATTT	100507650
rs183445783	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210713	GCCCAGGAGGTGGAG[C/G]TTGCAGTGAGCCAGG	100507650
rs183463805	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200454	CCTCAGCTTCCCAAG[C/T]AGATGGGATTACAGG	100507650
rs183535766	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23240093	AATGTGTGTTTATAT[A/G]TATATATATATACAC	100507650
rs183538755	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213106	TCACAAGGTCAGGAG[A/G]TCGAGACCATCCTGG	100507650
rs183660886	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193988	ATGGGATTACAGGAG[A/C]CTGCCGCTACGCCTG	100507650
rs183679022	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225134	CAGTTAAAATGGCTT[C/T]TATTCAAAAGTCAGG	100507650
rs183683023	snp	C/T	0.00597247	0.0543191	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236678	CTAATTTGGTAAATA[C/T]TGGTAGATGCAATTT	100507650
rs183690817	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210859	ATCCAGGAACTCTCT[C/G]TACTACCTTTGCAAA	100507650
rs183695112	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255786	AGACCAACCTCTTCA[G/T]GAGGCTGAGGGATTT	100507650
rs183702435	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23224787	AAGCTTCTGCACAGC[A/G]AAGGAAACAATCAAC	100507650
rs183708924	snp	A/C	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23255110	GCATAATAAAGAAGT[A/C]CCCTCTGCTTTACCC	100507650
rs183782971	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187842	GGGATCACTGCCTAT[A/G]GTCGATTAGATGGGG	100507650
rs183811370	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263276	CTCATGCTCCGAACA[C/G]GGAAAGTTGAGAGTG	100507650
rs183820973	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23222533	GAGACCCAATGGCTT[A/C]ATTGCTGAATTCTAC	100507650
rs183823321	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212947	CAGACATTATCATTT[A/G]TGATAATATCAGCAA	100507650
rs183828741	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23233658	GAGTTAGGGGAATCA[C/T]TCGGGCCTGGGAGGT	100507650
rs183830391	snp	A/G	0.00716266	0.059414	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208994	CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTT	100507650
rs183838899	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23261821	AAAAACAAAATTAGC[C/T]GGGCGTGGTGGAGGA	100507650
rs183848284	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23251972	TGGTAACTCTCTGAA[C/T]CGCCTTGTTCAGGAG	100507650
rs184008610	snp	A/G	0.00795532	0.062565	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196308	CTGCCCCGCTCCGCC[A/G]TTATCATGCCAAAAT	100507650
rs184019059	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215760	AAAGGAAATGATAAA[C/T]GAAAGACACATGGAA	100507650
rs184044610	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23226776	CCGTCTCCTCTCCTC[A/T]CTTCTTTTTTTTTCC	100507650
rs184144694	snp	A/G	0.0107246	0.0724382	intron-variant	RNF212B	GRCh38.p7	14:23244007	CACTTGAACCCAAAA[A/G]GCGAGGGTTGCAATG	100507650
rs184159236	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210376	TAGGCTTGGACTGTA[A/G]AACAGAGAAAGGATA	100507650
rs184192317	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203873	GTGTTCTCTGATCAC[C/T]GTATCCATGCCAACA	100507650
rs184215796	snp	G/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23232123	TCTGGGATGTGAGGA[G/T]CCCCTCTGCCCGGCT	100507650
rs184237296	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214865	ATAAGGCCACAAATT[C/T]AAAAAGCTGAGTGAA	100507650
rs184244162	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23221271	ACACGCTTCACTTAT[A/G]CAGATACACATAGAT	100507650
rs184245832	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199649	CAGGTAGGTCCCGAA[C/T]GAAGATTTTTAGCAG	100507650
rs184247489	snp	C/G	0.0704125	0.17392	intron-variant	RNF212B	GRCh38.p7	14:23232792	AGGGAGGTGGGGGGG[C/G]GGTCAGCCTCTGCCC	100507650
rs184252833	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23270749	GGGTAGTGGAATATA[A/G]CCAGTGAAGAACGAC	100507650
rs184336586	snp	A/T	0.00478085	0.0486577	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203396	GTGCGTGCAAATATC[A/T]TTTTTGTATAATGAC	100507650
rs184353590	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214460	AATTGCGCCAATGTA[C/T]TCCGGCCTGGGCAAC	100507650
rs184363458	snp	C/T	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23247123	CCAGCCTGGGCAACA[C/T]GAGCAAAACTCCATC	100507650
rs184367051	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247552	ACTAAGTATAATGCT[C/T]TCAAGTTTCATCCAT	100507650
rs184371101	snp	G/T	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23217991	AAAATTCAAGATAAT[G/T]CAGAGAGGAAATTCA	100507650
rs184378534	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218434	CTCTTAAAAGTAATC[A/T]CTTAAAAGTAGAATT	100507650
rs184379135	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23231210	GCTTTGGATGCTATT[A/G]TAAACAATATTAAGT	100507650
rs184388022	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23269297	GACAGAGTGAGACTC[C/T]GTCTCAAAAAACAAA	100507650
rs184391764	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23241527	TTCCCAGGTTCAAGC[A/G]ATTCTCATGTCTCAG	100507650
rs184488592	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23228656	TCTCTAAAAAAACAA[A/C]AAAACAAAACAAAAC	100507650
rs184490320	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198713	TATGTAAACACTATA[C/T]TCTAGCTGGTAAGTC	100507650
rs184815437	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202799	GAGGTTGCAGTGAGC[C/T]AAGATTGGTCACTGC	100507650
rs184816493	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216991	GGAGAGCAGATTAGT[A/G]ACTGACAGATGTTAA	100507650
rs184860949	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193014	GGAGAATCGCTTGAA[C/T]CTGGGAGGTGGAGGT	100507650
rs184902950	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23187461	TCAAGTGATCCTCCC[A/G]CCTCAGCCTCCCGAG	100507650
rs184945634	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23222058	ACTTCAAACAAATAA[C/T]CTAATGATTATCTTA	100507650
rs184960432	snp	A/T	0.0119091	0.0762411	intron-variant	RNF212B	GRCh38.p7	14:23251644	AACATGGTGAAACCC[A/T]GCCTCTACTAAAAAT	100507650
rs184985899	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195726	CTGATGGCACCTGGA[C/T]GGTGGAAGGGACTAG	100507650
rs184994460	snp	G/T	0.0115144	0.0749975	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212697	CACTATTCTCCTTTA[G/T]TTTTTAATTTAATAG	100507650
rs185008132	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23238765	AATAATAATAATAAT[A/C]ATAATAATAATAATA	100507650
rs185022502	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23226436	GAGATCGAGACCATC[C/T]TGGCTAACACGGTGG	100507650
rs185034149	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208426	AACTTGAGCCCAGGA[A/G]TTCAAGACTGCAATG	100507650
rs185039312	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23233260	AAGTACCCAGCGACA[C/G]AAACACTGCGGAAGG	100507650
rs185085028	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23229053	TTCCTGCTAACCTCT[A/G]ATCTACTTTCTGTCT	100507650
rs185089605	snp	G/T	0.0185938	0.0946107	intron-variant	RNF212B	GRCh38.p7	14:23262502	TTTATATGGAAACTT[G/T]GCTTCCATATTTTAG	100507650
rs185105657	snp	A/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237146	ATTTTTTTTTTTTTT[A/T]AAAGACGGAGTCTCT	100507650
rs185114540	snp	A/C	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23256694	TTCAAATTTTCTAAA[A/C]TAATTTTTTTAAGTT	100507650
rs185152651	snp	C/T	0.0197687	0.0974348	intron-variant	RNF212B	GRCh38.p7	14:23185781	ATAAGTGGCTTATTA[C/T]CATTGATTACTGGTG	100507650
rs185164096	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23223442	CTCACTGCAACCTCC[A/G]CCTCACGGGTTCACG	100507650
rs185167233	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254360	AAAACTAAAACTGGG[A/C]ATGGTGGCTCACTCC	100507650
rs185174100	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23235445	TACTGTTTTTACTTG[A/G]AAGAACATCTAACAT	100507650
rs185208896	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23242282	GTGGTTTGTCTCCGT[A/G]AAGCATATGCCATGT	100507650
rs185623480	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200005	CCCAAACTGTAGAAC[A/G]TAATAAAAAATTAAA	100507650
rs185627612	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215170	GATGGTTTAAAAGTG[G/T]TTGGCAGTTCCCCCC	100507650
rs185658714	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190713	ACTTTATTCTCTACA[A/C/T]GGCAGCCAGAATGAT	100507650
rs185666775	snp	C/T	0.0130921	0.0798413	intron-variant	RNF212B	GRCh38.p7	14:23229165	AATTTTTTCAAGATT[C/T]ATCCATGTTGTAGCA	100507650
rs185703879	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246628	AGAGACAGTCTTGCT[A/G]TATTGCCCAGGCTGT	100507650
rs185710396	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23225951	AAATATCTCATGTAC[A/C]CTGTAAGTATACACA	100507650
rs185720516	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194429	TGGGAGAAATTTTAA[C/T]GTACCTCTATTAGAA	100507650
rs185850866	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23268664	TTTCCATCTTAGAGG[A/G]GAAACCAAGGCACAG	100507650
rs185852778	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230977	TTCTGTTGGTCTATA[C/T]ATGTCTATCCTTATG	100507650
rs185857221	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211087	GCTGGTCGTGATGGC[A/G]TACGCCTGTAATCCC	100507650
rs185912617	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195283	AAAAAAAAAAACCCA[C/T]GAGATGCAGCTAAAG	100507650
rs185922791	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273245	ATACTCATCACTGTT[C/T]CATTTCTGGATTTCA	100507650
rs186004590	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200461	TTCCCAAGTAGATGG[C/G]ATTACAGGTGCGTGC	100507650
rs186013480	snp	A/G	0.000723432	0.0190051	intron-variant	RNF212B	GRCh38.p7	14:23244282	ATTTTATTTTATTCA[A/G]TTGTGGATATTCTCA	100507650
rs186017508	snp	A/C	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215521	TTAAACAAACAAACA[A/C]ACACACACACAAACA	100507650
rs186023148	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252943	ATGCTTAATTATAAC[C/T]ATATTTCTGTCCAGA	100507650
rs186024557	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23229690	CTATATCTTCTTTGT[A/G]GAAATGTCTATTCAA	100507650
rs186034993	snp	C/T	0.00835141	0.0640778	intron-variant	RNF212B	GRCh38.p7	14:23234332	CATGCAAAAAGTTTT[C/T]TTTAAAATTACTTAG	100507650
rs186044941	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215978	TTGCCGGGTGTGGTG[A/G]CTCATGCCTGTAATC	100507650
rs186095058	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259388	TTTTTTTGTAGAGAG[A/G]AGTCTCTGCATATTG	100507650
rs186118869	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200304	GCCATCAAATACCTA[C/T]AAGTTGGGTGAATTT	100507650
rs186149192	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219795	TTTTCTTTTAGTGTG[C/T]TTGTTTGTATATGCA	100507650
rs186153577	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23232260	CTGCCCCGCCGCCCC[A/G]TCTGGGATGTGAGGA	100507650
rs186158027	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229463	TTTTTGAGGAGCCAC[C/T]AAATTGCTTTCCAAA	100507650
rs186174809	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23253938	TTCAAAAATTAAATT[A/G]CGTGCAAAAATAAAT	100507650
rs186185710	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248529	TCACTGCAATCTCCG[A/C]CTCCCGGGTTCAAGC	100507650
rs186186941	snp	C/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23272441	CAACAAACAAACAAA[C/G]AAACAAACAACCGAA	100507650
rs186321400	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23234692	ACTTTAAATTACAGA[C/T]GTTTTATAATATATT	100507650
rs186526780	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23223193	GACAAACCATATGAT[C/T]ATTTCAATTGATGCT	100507650
rs186584151	snp	G/T	0.00636936	0.0560724	intron-variant	RNF212B	GRCh38.p7	14:23232162	TGGGAAGTGAGGAGG[G/T]CCTCTTCCCCGCCGC	100507650
rs186593598	snp	C/T	0.00716266	0.059414	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204948	AGGACTTTAAAAGCA[C/T]GTATAGAAAGATACA	100507650
rs186597008	snp	C/T	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23219556	GGCTCACTGCAACCT[C/T]TGCCACCTGGGTTCA	100507650
rs186672510	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209530	CATGCCTCCATACTG[A/T]TATAAACAAATGATT	100507650
rs186700064	snp	G/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23266362	TCCCAAATTTCCTAC[G/T]GTTATTGATTTTGAC	100507650
rs186705068	snp	A/G	0.00716266	0.059414	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210054	TACTGGGGAGGCTGA[A/G]GCAGGAAAATTGCTT	100507650
rs186744014	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209916	ACAGCACTTTGGGAG[A/G]CCGAGGTGGGCTGAT	100507650
rs186754566	snp	A/T	0.00716266	0.059414	intron-variant	RNF212B	GRCh38.p7	14:23227930	AATATAAAAGTTTTT[A/T]AAAAATCTCATCAGG	100507650
rs186760955	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198066	GGCTGTTTTTACTTC[C/T]TTTGTGGATCTTCAG	100507650
rs186765056	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213905	CCAACAGTCAACAGG[A/C]ACTAACATTTCAGTG	100507650
rs186770521	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23261515	GAACTCAGTCATTTC[C/T]TCTGTGAAGACTGCA	100507650
rs186782754	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211929	GACAGGGTTTTGCCA[C/T]GTTGGCCAGGCTGGT	100507650
rs186787497	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241100	GAAGAGGGACTTGGG[A/G]TAGGGTGTTTTGATC	100507650
rs186790018	snp	A/G	0.00398564	0.0444627	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184313	TGTGCAACAGAGCGA[A/G]ACCCCGTCTACTAAA	100507650
rs186837147	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237800	CCCTCTCCCGCCACC[G/T]CGAGCCGCTCCTAGC	100507650
rs186870966	snp	A/G	0.00438332	0.0466095	intron-variant	RNF212B	GRCh38.p7	14:23222824	TTGGGAGGCTGAGGC[A/G]GGGGGATCATCTGAG	100507650
rs186883510	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23188979	ACCAACTAATTGTAG[A/C]AAGATGTAGCTGTTG	100507650
rs186930670	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244927	CTTGATGTGTCATAT[A/G]TTGGCATACAATTGA	100507650
rs186985755	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23216473	ATTAAATTTAAATGG[C/T]TTAACTGTATCAATC	100507650
rs186991559	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23230393	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	100507650
rs186992718	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193406	TCAGGAATAAGGTAC[C/T]ACAACTAGAGACAGT	100507650
rs186994984	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23247783	TATTCCTCTTGGGTA[C/T]ATACCTACGAGTGGA	100507650
rs187001587	snp	C/T	0.00636936	0.0560724	intron-variant	RNF212B	GRCh38.p7	14:23226983	GGTGGCCTCACAAAT[C/T]TTTACATGTGATAAA	100507650
rs187015984	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210771	GACAGTGTGAGACTC[C/T]GTCTCAAAAAAAAAA	100507650
rs187022965	snp	C/T	0.0166325	0.0896639	intron-variant	RNF212B	GRCh38.p7	14:23245869	GGTTGGTTTTGCTTA[C/T]TGTTCTCTTTTAATA	100507650
rs187027545	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23266961	CTATTATTGTGGTTT[C/T]TGGTTTTTTGTTTTC	100507650
rs187032292	snp	A/T	0.0283406	0.115616	intron-variant	RNF212B	GRCh38.p7	14:23226000	AAATGAAAAATTTTT[A/T]AAAAAATTAAAAAAC	100507650
rs187037260	snp	A/G	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23257132	CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCA	100507650
rs187038969	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205894	AGTTTTGTAACTTCT[A/G]TGCCAAATTTTGACA	100507650
rs187177952	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271891	ATAATTGTTAACATT[G/T]GAGAGTTTTTTGGTA	100507650
rs187196765	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23239289	GGTCTTGAACTCCTG[A/G]CCTCAGGTGATCCAC	100507650
rs187204154	snp	A/G	0.00597247	0.0543191	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213017	AAGACCTGTACACTA[A/G]AAATTATAACACAGG	100507650
rs187327322	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202804	TGCAGTGAGCCAAGA[C/T]TGGTCACTGCACTCT	100507650
rs187337285	snp	C/G	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23217182	CTGACAGAGAAGCTC[C/G]TGGGTTTTAAGTTAA	100507650
rs187349508	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23246724	TGAGCCACCATGCCC[A/G]ATCTGAAAACTGTAC	100507650
rs187355883	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23254807	CTTCCATTACTGTGC[A/C]TCTCTCAGTATTTTT	100507650
rs187362127	snp	A/G	0	0	intron-variant	RNF212B	GRCh38.p7	14:23231063	AATATGAGTCTTCCA[A/G]ATTTTTTCCTTTTTA	100507650
rs187395509	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196563	TCCCGCCTCAGCCTC[C/T]TGAGTAGCTAGGACT	100507650
rs187463044	snp	A/G	0.0115144	0.0749975	intron-variant	RNF212B	GRCh38.p7	14:23232869	CCGTCTGGGAAGTGA[A/G]GAGCCCCTCTGCCCG	100507650
rs187476350	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23251570	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG	100507650
rs187539512	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208295	GGACGAGAAGATCAC[C/T]GGAGGCCAGGAGTTT	100507650
rs187553987	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207795	GACAACATGTGCCCA[A/G]GGTGGTCGGGGTACA	100507650
rs187555278	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185294	CAAGGCAGGGAATAT[A/G]TAGCACGAAACTCCA	100507650
rs187559096	snp	A/G	0.00716266	0.059414	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197616	AAATATAATTAAAAA[A/G]TAATAAAAAATATTG	100507650
rs187568779	snp	A/C	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23221139	CGCCTATAATCCCAG[A/C]ACTTTGGGAGGCTGA	100507650
rs187569234	snp	C/T	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23232364	AGGAGCCCCTCCACC[C/T]GGCAGCCACCCCATC	100507650
rs187571984	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249912	CAATTACAAATCTGA[A/T]CAAGTAACTGCCTTT	100507650
rs187573203	snp	C/T	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23232456	GCCCGGCAGCCGCCC[C/T]GTCTGAGAAGTGAGG	100507650
rs187701665	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23246425	CTGGGAAAACTGTTG[A/G]TGTAGAAATCTAATG	100507650
rs187796830	snp	A/C	0.0107246	0.0724382	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201065	TTAAGACTCTGAAAA[A/C]CAGAATAAAGGATCA	100507650
rs187799767	snp	A/G	0.00795532	0.062565	intron-variant	RNF212B	GRCh38.p7	14:23220774	AACTTGAAGTGAGCC[A/G]AGATTGCACCACTGC	100507650
rs187808520	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184921	TTAGCCTTATTAAAT[A/G]TATTATGCAAAATTA	100507650
rs187840960	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23255470	TACCAATAAAATGTT[A/G]GTATCAATGTTCCAA	100507650
rs187841796	snp	C/G	0.0119091	0.0762411	intron-variant	RNF212B	GRCh38.p7	14:23249340	TGCTTGAGGCCAGGG[C/G]TTTGAGACTAGCTTG	100507650
rs187961468	snp	A/C	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202005	CCTGTAATCCCAGCA[A/C]TTTGTGAGGCCGAGG	100507650
rs187980146	snp	A/G	0.0138799	0.0821421	intron-variant	RNF212B	GRCh38.p7	14:23230471	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	100507650
rs187984345	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267935	CTGCCTTTTAATTCA[C/T]TTACATTTAATGTAA	100507650
rs188096153	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236602	GGGGTTTATTATTGT[C/T]TTCAAATAATATTTA	100507650
rs188309925	snp	A/C/T	0.00755907	0.0610114	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210503	GTAGGATGGGGTGGG[A/C/T]GTGGTGGCTCACGCC	100507650
rs188331947	snp	C/G	0.00676609	0.0577691	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236112	AATATAGGACTCCAC[C/G]AGCTTTCTATTAAGC	100507650
rs188365719	snp	A/G	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23194193	GAAAATAGGTAGCAG[A/G]CAAGCACTACATAAA	100507650
rs188366562	snp	A/T	0.00115527	0.0240062	intron-variant	RNF212B	GRCh38.p7	14:23268909	ATCTCACAGGCTTAT[A/T]TTTATGCTTTCCAGA	100507650
rs188386774	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23225226	TGTAAATTAGTACAG[C/T]CACTGTGGAGAACAG	100507650
rs188401949	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212164	TTAGGAGAAAATTGT[A/G]GCCAGCCTTATACAT	100507650
rs188405342	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211012	ATCACGAGGTCAGGA[C/T]TTCGAGACCAGACTG	100507650
rs188407757	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23247203	ACTTTTTTTTTTAGG[A/T]CCACTAGTTTTCATG	100507650
rs188409469	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255820	AGATTGCTAACTATT[G/T]GTAATTTTTTAAAGT	100507650
rs188419038	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236688	AAATATTGGTAGATG[C/T]AATTTACATAAACAA	100507650
rs188420555	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195515	TTTTGTAATGCTCTT[C/T]CTTCATTATAGTCTC	100507650
rs188422556	snp	C/T	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23232066	TGCCCGGCTGCCACC[C/T]CGTCTGGGATGTGAG	100507650
rs188436542	snp	A/C	0.0142736	0.0832652	intron-variant	RNF212B	GRCh38.p7	14:23226037	GGGCGCGGTGGCTCA[A/C]GCCTGTAATCTCAGC	100507650
rs188456123	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23185970	CTGGGTGTGGTGGCT[C/T]ACGCCTGTAATCCCA	100507650
rs188462217	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240208	ACTTCTTTACAACCA[A/T]TTGGAATACCCACAA	100507650
rs188493713	snp	C/T	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23221693	AGAATACACATTCTT[C/T]TTTTTAGCGCATGGG	100507650
rs188551381	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244114	AACAACAGATGGAAG[C/T]ATTATTTGTGACCAC	100507650
rs188561296	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215180	AAGTGTTTGGCAGTT[C/T]CCCCCACCCCTCTGC	100507650
rs188565348	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23229166	ATTTTTTCAAGATTC[A/G]TCCATGTTGTAGCAT	100507650
rs188579728	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263313	GACATTTCACATTTA[C/G]CATATTGTTTAACAA	100507650
rs188590310	snp	A/G	0.00438332	0.0466095	intron-variant	RNF212B	GRCh38.p7	14:23192186	CCATCCTATTACTGG[A/G]TATATACCCAAAGGA	100507650
rs188631143	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23224346	ATATTATCTGACTTC[A/C]AATTATACTGCAGAG	100507650
rs188648848	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23261965	AGAGTGGGACTCTGT[C/T]TCAAAACAAACAAAA	100507650
rs188735856	snp	G/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23227837	CTCCTGGACTCAGGT[G/T]ATTCACCCACCTCAG	100507650
rs188746037	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208863	TCCCAGGTTCACGCC[A/G]TTCTCCTGACTCAGC	100507650
rs188764870	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260086	ATAACAAGCACACTA[C/T]AGTAAATGGATGAGG	100507650
rs188914456	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274076	TTTTTGGCCTTTTTA[C/T]TATTATTCTAGCATT	100507650
rs189046129	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215110	TCATGCGGGCAGTTT[C/T]CCCCATACTGTTCTC	100507650
rs189054283	snp	A/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199700	ATGAAGGAAAAATAG[A/T]GGGGAGGAAGGGAGA	100507650
rs189076977	snp	C/G	0.0115144	0.0749975	intron-variant	RNF212B	GRCh38.p7	14:23229119	TTATACAATATTTCT[C/G]TTTTTGTGTCTGGCT	100507650
rs189153634	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23233339	TATTGGCTGACCTTC[C/T]CTCCACTATTGTCCT	100507650
rs189219639	snp	A/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23253751	ATCAAGCAAATGATT[A/T]TCCAGATATATAGTT	100507650
rs189303476	snp	C/G	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23188312	CAGGCCAGATCTCCG[C/G]ATTTTCTTGATTCTT	100507650
rs189318508	snp	C/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23218472	CAGAAGAAAGAATTA[C/G]TGAGTTTGAAGACAA	100507650
rs189318970	snp	A/G	0.00993419	0.0697739	intron-variant	RNF212B	GRCh38.p7	14:23222640	CATTCTATGAGGCCA[A/G]TATTTCCCCTATACC	100507650
rs189331232	snp	A/G	0.0240643	0.107019	intron-variant	RNF212B	GRCh38.p7	14:23233872	GAAGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA	100507650
rs189333350	snp	A/G	0.00636936	0.0560724	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209005	CCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAGA	100507650
rs189334572	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23247578	TCCATGTTGTAGCAT[A/C]TCTGTTAGGACTTTA	100507650
rs189348946	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252176	CCCATTTTGATGCTA[C/T]CTAGGACCCACCAAG	100507650
rs189407766	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203515	ATGGAGCCTTGCTCT[A/G]TCACCCACGCTGGAG	100507650
rs189433684	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200007	CAAACTGTAGAACAT[A/G]ATAAAAAATTAAAAA	100507650
rs189455455	snp	A/G	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23222261	GACTGAATAAGAAAA[A/G]AAAAGAAGACCCAAA	100507650
rs189465055	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23257199	CAAAATTATTTTTCA[C/T]AGAGACAGGGTCTTG	100507650
rs189566665	snp	A/C	0.00716266	0.059414	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203893	CCATGCCAACATCTA[A/C]AGTTTTTTGATTTTT	100507650
rs189584402	snp	C/T	0.0217236	0.101931	intron-variant	RNF212B	GRCh38.p7	14:23232134	AGGAGCCCCTCTGCC[C/T]GGCTGCCCACTCTGG	100507650
rs189608388	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271084	ATGGGACTATGATTC[C/T]GATTCCAGCAACAAA	100507650
rs189708928	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23218165	CGAGGTCAGGAGATC[A/G]AGACCCTCTTGGCTA	100507650
rs189744024	snp	A/C			upstream-variant-2KB, intron-variant, utr-variant-5-prime	RNF212B	GRCh38.p7	14:23237917	CCACACCTCTCACAC[A/C]GCCTCGGCTGCGCCC	100507650
rs189844739	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212728	AGATGGAGTCTTGCT[A/G]TGTTGCCCAGGGTGG	100507650
rs189853607	snp	C/T	0.0119091	0.0762411	intron-variant	RNF212B	GRCh38.p7	14:23251646	CATGGTGAAACCCTG[C/T]CTCTACTAAAAATAC	100507650
rs189865551	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23239171	CAAGCAATTATCATG[C/T]CTCAGCTTCCCAAGT	100507650
rs189865786	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207810	AGGTGGTCGGGGTAC[A/C]GCTTAGTTTTATACA	100507650
rs189875916	snp	A/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185079	CCTTAAAATGAGGTT[A/T]GTTGAGCTATCATAG	100507650
rs189881835	snp	G/T	0.0123036	0.0774623	intron-variant	RNF212B	GRCh38.p7	14:23226570	CGGGAGGCGGAGCTT[G/T]CAGTGAGCCGAGATC	100507650
rs189966144	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211171	TGTGGTGAGCTGAGA[C/T]TGCACCACTGCCCTC	100507650
rs190107268	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209941	GCTGATCACTTGAAG[C/T]CAGGAGTTTGAGACC	100507650
rs190112640	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242592	TTGTACTCTTCCTCA[C/G]TCTTGTAAATGTACT	100507650
rs190129008	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23190714	CTTTATTCTCTACAC[A/G]GCAGCCAGAATGATC	100507650
rs190166429	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272664	AGATGTAGCAAATCC[C/T]AGTTTGGAAAAGTTA	100507650
rs190168479	snp	C/T	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23248681	TCCTGACCTCGTGAT[C/T]CGCCCACCTCAGCCT	100507650
rs190222188	snp	A/C	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23228685	ACAAAACAAAAACAC[A/C]AGAAGAAGAAAGAAC	100507650
rs190226756	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225979	ACACCAAGTATGTAC[C/T]CACAAAAATGAAAAA	100507650
rs190230682	snp	A/C	0.0433465	0.140692	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194747	CTCAAAAAAAAAAAA[A/C]AAAAAAAAAACAACG	100507650
rs190236231	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198726	TACTCTAGCTGGTAA[A/G]TCTGTTTCTCATGGT	100507650
rs190278370	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23230446	GATCACGAGGTCAAG[A/G]GATCGAGACCATCCT	100507650
rs190313667	snp	A/T	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23246036	TGTGCTAATAGTTGA[A/T]CAAGCTGACTGTTTT	100507650
rs190315258	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23267430	TGCCTTTGTCTCTTG[C/T]AACAATTTTTTTTTT	100507650
rs190378925	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23262612	ATCCTCTAAAGTGGC[A/C]CTTGACCTCTGCCTA	100507650
rs190402929	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237198	GCAGTGGCGCGATCT[C/T]GGCTCACTGCAACCT	100507650
rs190403912	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23234402	TCCTAGGAAGATTTC[C/T]TGCACACCTAGGTTA	100507650
rs190459867	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214495	TGAGACTCAGTCCCC[C/T]CAATAATTAAATTAA	100507650
rs190505249	snp	C/T	0.00716266	0.059414	intron-variant	RNF212B	GRCh38.p7	14:23241666	CGGCCTCAAGTGATC[C/T]GCCTGCCTCAGCCTC	100507650
rs190622696	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183402	GTAGTTTTCATTAAC[A/G]GTAGGAAAAAAGAGC	100507650
rs190659084	snp	A/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23256957	CAGGAGTTCGAGACC[A/T]GTCTGACCAACATGG	100507650
rs190781413	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210306	GAAAGATTGAGAAAC[C/G]GTCTCTGACCAGAGA	100507650
rs190789658	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191997	CTGCCCTTTCAGGCC[A/G]TGCATTCAAGAATAT	100507650
rs190793148	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23229917	GTAAGATGGTTATGA[G/T]CTTGATACTGCATAA	100507650
rs190795289	snp	A/C	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23235538	CCACTTCAAGGAAAA[A/C]CAGTGACAGTATTTG	100507650
rs190800136	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200578	TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT	100507650
rs190804607	snp	C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23216016	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGA	100507650
rs190809055	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254410	GGATGACATGAGGCC[A/C]GAAATTTGAGACCAG	100507650
rs190810588	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266453	TTTCTTTCTTGTTGC[C/T]CAGGCTGGAGTGCAG	100507650
rs190811146	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23223515	GCCCGCCATCAAGCC[C/T]GGCTAATTTTTTTGT	100507650
rs190825031	snp	A/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23245353	AACATTATAAGTATA[A/T]TAAAATCCAGCTGAG	100507650
rs190907485	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196305	AGCCTGCCCCGCTCC[A/G]CCATTATCATGCCAA	100507650
rs190942025	snp	A/C	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23220803	GCACTCCAGCCTGGG[A/C]GACAGAGCAAGACTC	100507650
rs190977743	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249590	GTATTTAGTTTGATA[A/T]TATTTTACCTAAAAA	100507650
rs191039019	snp	G/T	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23219558	CTCACTGCAACCTCT[G/T]CCACCTGGGTTCAAG	100507650
rs191044996	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232166	AAGTGAGGAGGGCCT[A/C]TTCCCCGCCGCCATC	100507650
rs191049317	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205083	CCTCCTTCTTAATCA[A/G]CCAGTCATTTTTATT	100507650
rs191077423	snp	C/G/T	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23248351	ATGTTGCCCAGGTCT[C/G/T]GAACCCCTGGGCTCA	100507650
rs191079325	snp	C/T	0.0154538	0.0865337	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206153	GATCTCATCTCACTG[C/T]AACCTCTGCCTCCTG	100507650
rs191083795	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23272193	GAGGCCGAGGCGGGC[A/G]GATTATGAGGTCAGG	100507650
rs191093518	snp	A/G	0.239326	0.249772	intron-variant	RNF212B	GRCh38.p7	14:23232292	CGCCTCTGCCCGGCC[A/G]CAACCCCATCTGGGA	100507650
rs191108051	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260555	AGTCTTAGCAACCAT[G/T]ACTAAGGGGCACTGA	100507650
rs191214473	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216910	AAAAAAAAAAGACCA[A/G]TCTCAAAGGTTACAG	100507650
rs191217424	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273842	CTGAAGCCTCAGAAA[C/T]TTTAGTCATTATCAT	100507650
rs191219417	snp	A/C	0.0115144	0.0749975	intron-variant	RNF212B	GRCh38.p7	14:23232373	TCCACCTGGCAGCCA[A/C]CCCATCTGAGAAGTG	100507650
rs191230671	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234693	CTTTAAATTACAGAC[A/G]TTTTATAATATATTT	100507650
rs191244685	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241226	TTTAAGAGAACAGCA[C/T]GTACAAAGACATATT	100507650
rs191250786	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23261684	TTTTTAGTATCGGCT[C/G]GGTGTGGTGGCTCAC	100507650
rs191281786	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184474	GCCTGGGAGGTAGAG[C/G]AAGACCCTGTCTCAA	100507650
rs191304764	snp	A/G	0.00874735	0.0655527	intron-variant	RNF212B	GRCh38.p7	14:23220537	ACTCTGTCTCAAAAA[A/G]CAAAACAGCCGGGCT	100507650
rs191431418	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23223205	GATCATTTCAATTGA[A/T]GCTGAAATAGCACTT	100507650
rs191602589	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23228173	GGAGGTGGAGATTGC[A/G]GTGAGCTGAGATCGT	100507650
rs191678633	snp	A/T	0.0130921	0.0798413	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197674	AAAGGAGAGAGAATA[A/T]TACAATGAACTCTCA	100507650
rs191711712	snp	A/G	0.00478085	0.0486577	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213585	CTTCCACCCCGACTC[A/G]GCAGCAAGAAGGTGG	100507650
rs191723126	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222828	GAGGCTGAGGCGGGG[A/G]GATCATCTGAGGTCA	100507650
rs191727188	snp	C/T	0.00330659	0.040526	intron-variant	RNF212B	GRCh38.p7	14:23240324	TAGGTTATTCTTACT[C/T]TTTCTCTTTATCTGC	100507650
rs191728626	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23189050	ATCAAGGTTTTGACT[A/T]TGAAGATTATTTTAT	100507650
rs191812992	snp	C/T	0.00795532	0.062565	intron-variant	RNF212B	GRCh38.p7	14:23193491	AGAGGGAGGGCAGAA[C/T]GGAGGACTCAAGAGG	100507650
rs191825632	snp	A/C	0.0126979	0.078662	intron-variant	RNF212B	GRCh38.p7	14:23225083	ATGCCACCCCACACA[A/C]AAAAAAAACACCTAC	100507650
rs191833909	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236641	AAATAATAAATATTT[A/T]AAAATTTCTCACTTT	100507650
rs191837104	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210828	CATTAGGGAAAACTG[A/T]AACTGGGTGAAGGAT	100507650
rs191859616	snp	C/T	0.0240643	0.107019	intron-variant	RNF212B	GRCh38.p7	14:23229496	AGGTGCATCATTGTA[C/T]ATTCCCATCAGCAAT	100507650
rs191881955	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23246998	ATAAAAAATTAGCCA[A/G]GTGTGGTGGCACGTG	100507650
rs191899734	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23231090	TTTAAGATTGTTTTG[A/G]CTATTCTAAGTTTTT	100507650
rs191917856	snp	A/G	0.00636936	0.0560724	intron-variant	RNF212B	GRCh38.p7	14:23269071	GCACTTTGGGAGGCC[A/G]AGGAGGGTGGATCAC	100507650
rs191991051	snp	G/T	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23239695	ACGGTCTCAGCTCAC[G/T]GCAACCTCTGCCTCC	100507650
rs191999013	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213100	GGCATATCACAAGGT[C/G]AGGAGATCGAGACCA	100507650
rs192029820	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209565	AAAAGACTAAATGGT[A/G]GAGTGGAAACAAATC	100507650
rs192168104	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212B	GRCh38.p7	14:23251688	GGGTGTGGTGGCGGG[C/T]GCCTGTAATCCCAGC	100507650
rs192171099	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23244726	CTAAAAATTGCTTTG[A/G]GTATATAGGCCTGGC	100507650
rs192175180	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215690	GGAAAACTAAGAAAA[C/G]GGGTCATGAGCAGAT	100507650
rs192273790	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203378	TTGTGCTGCTATAAA[C/T]ATGTGCGTGCAAATA	100507650
rs192282976	snp	A/T	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23217679	AGACCACCAAGGTGG[A/T]ACTTCTATGAGTCTG	100507650
rs192306359	snp	A/C	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196673	TCTTGAACTCCTGGT[A/C]TCAAGCAATCCTCCT	100507650
rs192342238	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23227050	TAATGAAATCAGTAA[C/T]GTCATGAGGTCTATG	100507650
rs192355680	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259394	TGTAGAGAGGAGTCT[C/T]TGCATATTGCCCAGG	100507650
rs192468591	snp	A/G	0.0111196	0.0737302	intron-variant	RNF212B	GRCh38.p7	14:23225487	GCCATAAACAAGAAT[A/G]AGATTCTGTCATTTG	100507650
rs192476644	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211021	TCAGGACTTCGAGAC[C/T]AGACTGGCCAACATA	100507650
rs192481286	snp	C/T	0.0225045	0.103662	intron-variant	RNF212B	GRCh38.p7	14:23256485	CAAGTGATTCTCCTG[C/T]CTCAGCCTCTCCATT	100507650
rs192492093	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236724	CTTTGGAGGGTCTTC[A/G]ATAATTTTGTAAAGG	100507650
rs192510964	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198415	CCAAGCGTGGTGGCT[C/G]ACGCCTGAAATCTGA	100507650
rs192523647	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208361	AATTAGTCCAGAGTG[A/G]TGGTGTGTGCCTGTA	100507650
rs192542638	snp	C/T	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185556	TAATGTGGGATAAAA[C/T]ATGAATGTGATGAAT	100507650
rs192565384	snp	A/C/G	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23221190	TCAGGAGTTTGAGAC[A/C/G]AGCCTGGCCAGCATG	100507650
rs192571152	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250124	TTCAGTTCTTTGCAG[C/T]TCTTTTACAGACCAT	100507650
rs192573692	snp	G/T	0.0236746	0.106192	intron-variant	RNF212B	GRCh38.p7	14:23232735	CCGTCCGGGAGGGAG[G/T]TGGGGGGGTCAGCCC	100507650
rs192587079	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274330	GCTGGACAGGAGGTA[A/G]TTAACAGGTTTGTAA	100507650
rs192647066	snp	A/C	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23233027	GTCTGTGTAGAAAGA[A/C]GTAGACATAGGAGAC	100507650
rs192804119	snp	G/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214425	CTTGAACCCAGGAGG[G/T]GGAGGTTGCGGTGAG	100507650
rs192809507	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23255004	ACCAAACCAAAATGG[A/G]ATTACTCATGCTGAC	100507650
rs192882372	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251573	GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCGG	100507650
rs192886508	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221739	GACGATATGTTAGGT[C/T]ACCAAACAAATCTGA	100507650
rs192932366	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201380	AAGGGAATTTGTTAC[A/C]TCTGTGGCACACAGT	100507650
rs192952786	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255774	GAAAAACGAAAGAGA[A/C]CAACCTCTTCATGAG	100507650
rs192978828	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23192966	GCATGGTGGCACATG[C/T]CTGTAATCCCAGCTA	100507650
rs192999302	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23224690	TCCAGGACACTGGTC[C/G]GGGCAAAAATTTCTT	100507650
rs193062932	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202417	GCCCTTACAATCTTT[A/G]ATCTTATGTGCCCAC	100507650
rs193072721	snp	G/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23268584	TTTTGTTGATGTCAC[G/T]CCTAGCTAATTTTTG	100507650
rs193111865	snp	G/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214585	CAGACCTGAATAATA[G/T]AACCAAAAAAATGTT	100507650
rs193124069	snp	C/G	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23241884	GTCGGGAGATTGAGA[C/G]CATCCTGCTAACACG	100507650
rs193199301	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236312	TGATGTCAGGAGTTC[A/G]AGAGCAGCCTGGCCA	100507650
rs193201985	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210515	GGGCGTGGTGGCTCA[C/T]GCCTATAATCCCAGA	100507650
rs193230953	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23216968	TTAAATGATAAAATT[A/G]TAGAACTGGAGAGCA	100507650
rs193239456	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23194321	AAGAAGATATGACAA[C/T]CTTGAACTTCTAAGT	100507650
rs193241107	snp	A/C/T	0.0225045	0.103662	intron-variant	RNF212B	GRCh38.p7	14:23246463	CGGCCTGCTAACTTA[A/C/T]AGCTTTATTTCTTTG	100507650
rs193271486	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198890	ATAGAATGAGCCCTT[A/G]GGTAGTGGATTAGAG	100507650
rs193275865	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23228938	TTAGGTACATTCACA[A/G]TGTTGTACAATCATC	100507650
rs193276887	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23262061	AGTCCTGCATTATGG[A/G]TTAAAGAGACACTGC	100507650
rs199512076	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23234199	TCTATTAAGTTGTTG[A/G]TTTTCTTTTTTAAAA	100507650
rs199560542	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23222256	GCCAGACTGAATAAG[-/A]AAAAAAAAAGAAGAC	100507650
rs199650053	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23217255	CAGTGGTGGCAGTGG[G/T]GGGGGGGGGGCTCCT	100507650
rs199663943	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23240048	TCAAAAAAAAAAAAA[-/T]CTCACCACTGTCTGT	100507650
rs199665900	in-del	-/CAGTGGTGG			intron-variant	RNF212B	GRCh38.p7	14:23217231	AGAACCACCATAGAC[-/CAGTGGTGG]CAGTGGTGGCAGTGG	100507650
rs199807468	in-del	-/TATT	0.0174175	0.0916809	intron-variant	RNF212B	GRCh38.p7	14:23233422	AAAAAAAAAAAAGAA[-/TATT]TAAAGAAAAGAAAAT	100507650
rs199843559	in-del	-/T	0.00716266	0.059414	intron-variant	RNF212B	GRCh38.p7	14:23187595	GCACTCCATTCCTGA[-/T]TTTTTTTTTCTAGAT	100507650
rs199883971	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236472	GTGAGCCGAGATGGC[A/G]CCACTGCACTCCAGC	100507650
rs199917772	in-del	-/AAAAAAAC/CT			intron-variant	RNF212B	GRCh38.p7	14:23228645	AGAGCAAGACTCTCT[-/AAAAAAAC/CT]AAAAAAACAAAAAAA	100507650
rs200133732	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237790	TCTCCTACACCCCTC[C/T]CCCGCCACCGCGAGC	100507650
rs200134695	in-del	-/TTC			intron-variant	RNF212B	GRCh38.p7	14:23226800	TTTTCCTTTCCTTCT[-/TTC]TTCTTCTTCTTCTTT	100507650
rs200191476	in-del	-/A	0.00597247	0.0543191	intron-variant	RNF212B	GRCh38.p7	14:23218846	GTACAGGAAAGTTAT[-/A]AGAACACCAAACAGA	100507650
rs200197774	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23217256	AGTGGTGGCAGTGGT[G/T]GGGGGGGGGCTCCTC	100507650
rs200206625	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23227233	TTATAATTTTTTTTT[A/C]GGTAAAACGGAGTAG	100507650
rs200216174	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23193119	AAAAAAAAAAAAAAA[A/G]AATGTTACCAGAATG	100507650
rs200238810	in-del	-/C			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185265	AACAACAAACAACAA[-/C]AAAAAAAACCAGACA	100507650
rs200252051	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23242223	CTTTTAAAGTTCGCT[-/A]ATGTAAAAAGCTGTT	100507650
rs200310726	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23257160	TCAGTCACACACACA[-/C]AAAAAAAATAAAATA	100507650
rs200313084	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23232334	TCTCTGCCCGGCTGC[A/C]CTGTCTGAGAAGTGA	100507650
rs200363333	snp	G/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214882	AAAAGCTGAGTGAAC[G/T]TCAAGAAGAATAAAC	100507650
rs200415578	in-del	-/T	0.370974	0.218781	intron-variant	RNF212B	GRCh38.p7	14:23242215	TCATGACCTTTTAAA[-/T]GTTCGCTAATGTAAA	100507650
rs200427533	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23239968	TATTAATCCAGAAAA[-/C]CTGGGGGAAAAAAAA	100507650
rs200514077	in-del	-/G	0.0134861	0.0810011	intron-variant	RNF212B	GRCh38.p7	14:23248303	GGCTAGTTTTTGTGT[-/G]TTTTTTTTTTTTAAT	100507650
rs200562249	in-del	-/TC			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236954	GCCAATCTTATTCTG[-/TC]TCTCTCTTTTTTTTT	100507650
rs200575736	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23241488	GAATGCAGTGGCACA[A/G]TCTTGGCTCACTGCA	100507650
rs200579319	in-del	-/G	0.00914312	0.0669923	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185244	GAAAGACTCAGCAAA[-/G]AAAAAAACAACAAAC	100507650
rs200698480	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23226292	ACAGAGCAAGAAACC[A/G]TCTCAAAAAAAAAAA	100507650
rs200877658	in-del	-/GTTT			intron-variant	RNF212B	GRCh38.p7	14:23227618	TTTTTTTGTTTGTTT[-/GTTT]TGAGACTAGTTCTCG	100507650
rs200921236	snp	A/C/T	0.0240643	0.107019	intron-variant	RNF212B	GRCh38.p7	14:23257162	AGTCACACACACACA[A/C/T]AAAAAATAAAATAAA	100507650
rs200965876	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23257387	TAAAAATGAGGGTTT[-/A]AAAAAATAGACTAGA	100507650
rs201031774	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23243716	AAAAAAAAAAAAAAA[A/G]AAAGCAAGCAAGCAA	100507650
rs201058706	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23217261	TGGCAGTGGTGGGGG[A/G]GGGGCTCCTCTGCCT	100507650
rs201138786	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23224236	TGTCAAAAAAAAAAA[-/A]GCTATCCTAAAATTT	100507650
rs201140593	in-del	-/A	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23221060	GTGGCTGAATGGATG[-/A]AAAAAAAGACACAAT	100507650
rs201169651	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23186015	TGAGGTGGGAGGATC[A/G]TGTGAGCCATGGAGG	100507650
rs201181337	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206923	CGTTAAAAAAAAAAA[-/A]GACAAGGTCTTAGAA	100507650
rs201183501	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23238776	AATAATAATAATAAT[-/C]AATAATCCCACAAAG	100507650
rs201288379	snp	A/C			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185252	TCAGCAAAAAAAAAA[A/C]AACAAACAACAACAA	100507650
rs201288815	in-del	-/CTT	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23219462	AAGTGTAGCGCTCTC[-/CTT]CTTCTCCTTCTAGTT	100507650
rs201394410	in-del	-/T	0.0182019	0.0936463	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203241	ACATATGATGTTTGG[-/T]TTTTCCATTCCTGGG	100507650
rs201446994	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23264778	TCACTTGTTTTTTTT[A/G]CCTGACAGTGATTCC	100507650
rs201494532	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23266405	AAATCCTTTTAAATG[-/T]TTTTTTTTTTTTTTT	100507650
rs201635862	in-del	-/AAA			intron-variant	RNF212B	GRCh38.p7	14:23223055	GTGAAACTCCGTCTC[-/AAA]AAAAAAAAAAAAAAG	100507650
rs201656139	in-del	-/T/TTT			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236959	CTTATTCTGTCTCTC[-/T/TTT]TCTTTTTTTTTTTTT	100507650
rs201666883	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23263748	TGACATGTGCCCCTT[-/C]CCCCCAAAAAAAACG	100507650
rs201676641	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23266406	AATCCTTTTAAATGT[G/T]TTTTTTTTTTTTTTT	100507650
rs201704825	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23226809	CCTTCTTTCTTCTTC[-/T]TTCTTTTTTTTTTTT	100507650
rs201735838	in-del	-/GTGGCAGTGG			intron-variant	RNF212B	GRCh38.p7	14:23217245	CCAGTGGTGGCAGTG[-/GTGGCAGTGG]TGGGGGGGGGGCTCC	100507650
rs201824962	in-del	-/A/AAAAA/AAAAC	0.0964829	0.200564	intron-variant	RNF212B	GRCh38.p7	14:23220822	GAGCAAGACTCCATC[-/A/AAAAA/AAAAC]AAAAAAAACAAAACA	100507650
rs201834355	in-del	-/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206083	AGCATTTGACTAGTC[-/T]TTTTTTTTTGAGACG	100507650
rs201908773	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23225081	TGATGCCACCCCACA[-/C]AAAAAAAAAACACCT	100507650
rs201949788	in-del	-/AAT/C/CATCATCAT			intron-variant	RNF212B	GRCh38.p7	14:23238773	AATAATAATAATAAT[-/AAT/C/CATCATCAT]AATAATAATCCCACA	100507650
rs201979271	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23243717	AAAAAAAAAAAAAAA[A/C]AAGCAAGCAAGCAAG	100507650
rs201981562	in-del	-/G	0.487809	0.0771174	intron-variant	RNF212B	GRCh38.p7	14:23266412	TTAAATGTTTTTTTT[-/G]TTTTTTTTTTTTTTT	100507650
rs201994683	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23228108	GGTGGCACATGCCTG[C/T]AATCCCAGCTACTCA	100507650
rs202003841	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23218877	TTTAACCCAAAGAAG[A/T]GTACCTCCGGGCATT	100507650
rs202018597	in-del	-/A			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185262	AAAACAACAAACAAC[-/A]AACAAAAAAAACCAG	100507650
rs202077376	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23257158	ACTCAGTCACACACA[-/C]ACAAAAAAAATAAAA	100507650
rs202113448	snp	A/C			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185241	AATTGAAAGACTCAG[A/C]AAAAAAAAAACAACA	100507650
rs202155697	in-del	-/C	0.0126979	0.078662	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273283	CTTTGGATATACTGT[-/C]CCATTGCCAATGTTA	100507650
rs202192926	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23217256	GTGGTGGCAGTGGTG[-/A]GGGGGGGGGCTCCTC	100507650
rs202210969	in-del	-/A	0.137187	0.223099	intron-variant	RNF212B	GRCh38.p7	14:23269725	CAAAAAAAAAAAAAG[-/A]AAAAAATTATCATCA	100507650
rs202240994	snp	A/G	0.00299548	0.0385846	intron-variant	RNF212B	GRCh38.p7	14:23262715	CATCACAGTCAGGTG[A/G]AGAACATTTTTCCCC	100507650
rs367582394	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23230426	TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT	100507650
rs367596830	snp	A/G			missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240425	GTGGCCATATTTTCT[A/G]TAAAAAGTGTGTGAC	100507650
rs367621233	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197054	GCCTAGGACTAAGTA[A/G]GTACCCAATTTAAAA	100507650
rs367726814	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244130	ATTATTTGTGACCAC[C/T]GTTACAGAAGCACAA	100507650
rs367758499	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23245908	TAAGTAGTGGACGCT[C/T]AAGACGTTGTCATTG	100507650
rs367772394	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205498	ACCTAGATTATTTAC[A/G]AAAACTGTGATAGTC	100507650
rs367798024	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200546	GGCCAGGCTGGTCTC[A/G]AACTCCTGGCCTCAA	100507650
rs367958948	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23231660	CGGTCTCCCTCTCCC[G/T]CTCTTTCCATGGTCT	100507650
rs368094093	in-del	-/GT	0.0310518	0.120672	intron-variant	RNF212B	GRCh38.p7	14:23234297	TGTGCTTTACTTTTC[-/GT]GTGTGTGTGTGTGTG	100507650
rs368116463	in-del	-/T	0	0	intron-variant	RNF212B	GRCh38.p7	14:23234335	GCAAAAAGTTTTTTT[-/T]AAAATTACTTAGTCA	100507650
rs368158713	snp	A/G			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236395	TGGCAGGCGCCTGTA[A/G]TCCCAGCTACTCAGG	100507650
rs368162915	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206047	TTTATTAAAGATTTT[A/G]CTTATTACATAAACC	100507650
rs368178670	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201410	TAATTTTAACTTAAC[A/G]TAACAATTATTGTTA	100507650
rs368284665	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23217790	ACAAGCCCAGACCAC[G/T]AAGACTATAATAACG	100507650
rs368312380	snp	A/G	0.0103295	0.0711199	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209205	GGTGGGAGTGTAGCA[A/G]TAAGGACGACCAGAG	100507650
rs368339553	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184725	AACATACTTGTTGAT[A/G]TTAGAATAACTAGCT	100507650
rs368374111	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23223104	TCATCATGATCAACT[A/G]AGATCTCAGGGATGC	100507650
rs368443713	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196629	AATATTTTTATAGAG[A/G]TGGGGTCTTGCTATG	100507650
rs368498650	in-del	-/TGT	0.499653	0.0131743	intron-variant	RNF212B	GRCh38.p7	14:23231947	TCACTCAGTGCTCAA[-/TGT]TGTTGCCCAGGCTGG	100507650
rs368498700	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273456	ATAGTAAAATAAAGA[C/T]GATGCCCTTTTATTG	100507650
rs368615633	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212918	TTCTTTTTTGCCAGC[C/T]TAATAGTAGATTTCA	100507650
rs368665198	snp	A/C			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184437	AGGCTGCAGTGAGCT[A/C]TGATGACGCCACTGC	100507650
rs368671411	snp	C/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199384	TTCCAAAGGAGGCAA[C/T]CAGATATGCATCTAT	100507650
rs368687527	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197940	TTGTTCTCTGGTGGG[C/T]AGGCGGGGATCTCAC	100507650
rs368748978	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23248535	CAATCTCCGCCTCCC[A/G]GGTTCAAGCAATTAT	100507650
rs368761633	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208980	AGCCGGGATGGTCTC[C/G]ATCTCCTGACCTCGT	100507650
rs368800812	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23269613	GCTACTTGGGAGACT[A/G]AGACAGGAGGATCAC	100507650
rs368819437	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23219030	TACAAGCCCGGAGAG[A/T]GTGGCATGACATATT	100507650
rs368820298	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23188677	GTCTTACTGCATTAC[A/C/T]CAGGCTGATCTCAAA	100507650
rs368911212	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23233598	AATAGAAAAATTAGC[C/T]GGGTATGGTGGTGCA	100507650
rs368976716	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197251	ATAACGAGAGGCCAG[A/G]CACTGTGGCTCACGC	100507650
rs368988721	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23185886	AGGTGGAGTGCTTGA[A/G]CTCAGGAGTTCAAGA	100507650
rs369025870	snp	C/T	0.000798403	0.0199641	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240440	GTAAAAAGTGTGTGA[C/T]TCTGGGTGAGTGACT	100507650
rs369041359	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203293	TCTCCAATCTCATCT[A/G]CCACAATTTCTTTAT	100507650
rs369128323	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214990	GCTAGAGAGGAATGA[C/T]ACATTACTGATATGA	100507650
rs369169503	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23249503	TGAGCCATGATTGCA[C/T]CACCATACTCCAGCT	100507650
rs369173726	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23232481	GTGAGGAGCCCCTCC[A/G]CCCGGCAGCCGCCCC	100507650
rs369185033	in-del	C/GG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198544	AGCTGGGCGTGGTGG[C/GG]GGGTACCTGTAATCC	100507650
rs369192250	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23187090	GCCATATCCCAAGTA[A/C/T]GTAGTACAATTCTGT	100507650
rs369222116	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191423	CTTTTATAATATCTG[A/C]CATTACTTAACATAA	100507650
rs369248900	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23223049	ACAAGAGTGAAACTC[C/T]GTCTCAAAAAAAAAA	100507650
rs369283082	snp	A/G	0.00795532	0.062565	intron-variant	RNF212B	GRCh38.p7	14:23241667	GGCCTCAAGTGATCC[A/G]CCTGCCTCAGCCTCC	100507650
rs369362642	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23186218	AATCTTTTTGTGACA[G/T]AAACTCTTAAGTGTG	100507650
rs369383094	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23253153	TCAGTGTGTATCTCT[A/G]AAAGATAGGAACTTT	100507650
rs369389632	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23230172	AAGGAAGAGAGAGAG[A/T]GTTGTAGTTCTTTTT	100507650
rs369397829	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210047	TCCCAGCTACTGGGG[A/G]GGCTGAGGCAGGAAA	100507650
rs369412194	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242792	CAGCTTGAGCAACAT[A/G]GGGAGACTCCATCTC	100507650
rs369418429	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23253850	ACTAATAGGTTTTGA[A/C]TGTCAAAGAGATCGT	100507650
rs369427035	snp	G/T	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23228199	ATCGTGCCATCACAC[G/T]CCAGCCTGGGTGACG	100507650
rs369432907	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23242240	GTAAAAAGCTGTTTA[-/A]CTATGGTAACAGCAG	100507650
rs369438166	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23267712	GAGGATTACAGGCAT[A/G]AGCCACTGTGCCTGG	100507650
rs369447344	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193231	CAACTCAGAAAATTA[C/T]ACATAGCCAAAGTAT	100507650
rs369504170	in-del	-/AG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213687	TTAGGAACTGTGTGC[-/AG]TCTACCTAAACAGGG	100507650
rs369539143	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242008	AATGGTGTGAACCCC[A/G]GAGGCAGAGCTTGCA	100507650
rs369545176	snp	A/C	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23224781	GTTAAAAAGCTTCTG[A/C]ACAGCAAAGGAAACA	100507650
rs369585930	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23191836	TTGGCATATAGAAGG[C/G]ACTCGACAAATACAT	100507650
rs369734828	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242125	AAAGAAAAAGAAAAA[A/G]AAAAACCTTTAGTCC	100507650
rs369819691	in-del	-/TC			intron-variant	RNF212B	GRCh38.p7	14:23191466	TTGTTCCTTGTTTGT[-/TC]CTTTCCTATTAAAAT	100507650
rs369828797	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213355	CTGAGAGAAATTAAA[C/G]AAGACCTAAATAAAT	100507650
rs369842553	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23218229	AAAAATTAGCCGGGC[A/G]TGGTGGCACACACCT	100507650
rs369879418	in-del	-/AG			intron-variant	RNF212B	GRCh38.p7	14:23255056	AATCAGGAGAGAGAG[-/AG]GTAATAGCTAAATCT	100507650
rs369910580	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23257386	TTAAAAATGAGGGTT[-/T]AAAAAAATAGACTAG	100507650
rs369980012	snp	C/G	0.00438332	0.0466095	intron-variant	RNF212B	GRCh38.p7	14:23265222	TCTGGTCAGGAGATG[C/G]AGGATAACTTTTCAG	100507650
rs370064324	snp	A/G/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214910	AACCCAAATAAATCC[A/G/T]TGCCAAGACATATCA	100507650
rs370084284	in-del	-/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203482	TACTTTTAGTCCCCC[-/T]TTTTTTTTTTTTTTG	100507650
rs370177567	in-del	-/CCT			intron-variant	RNF212B	GRCh38.p7	14:23219470	CGCTCTCCTTCTTCT[-/CCT]TCTAGTTTTTTTTTT	100507650
rs370180290	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203724	CTCATGTGATCCACC[C/T]GCCTTGGCCTCCCAA	100507650
rs370191245	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272950	CTGTAGCTTCCAGTA[C/T]GCATTAGGGGTGATG	100507650
rs370312821	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23271042	TTTACTTCTCCAGAG[A/G]CCGCTAGAATAATAT	100507650
rs370334113	in-del	-/CTCCC			intron-variant	RNF212B	GRCh38.p7	14:23226758	CTCCCCTCCCCTCCC[-/CTCCC]GTCTCCTCTCCTCTC	100507650
rs370391535	snp	A/T	0.000873076	0.0208752	intron-variant	RNF212B	GRCh38.p7	14:23243332	TTCTCCCCCTGCCAC[A/T]AACTGTCTCATCCCA	100507650
rs370432041	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183534	CCGTCTTCTGCTTCC[A/G]CCTTTCCCAGGTGTC	100507650
rs370482885	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23245931	TGTCATTGAATGAAT[A/G]AATGAATGGAATGTT	100507650
rs370655185	snp	A/G			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194927	ATTTCGATTTACTGG[A/G]TCACAGAGGAGCTCT	100507650
rs370679986	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202455	GTGATAGTCCCTGGG[A/C]CTTGAGGAGTTGAAT	100507650
rs370756607	multinucleotide-polymorphism	ATTTTA/TTTTTT			intron-variant	RNF212B	GRCh38.p7	14:23264823	ATATTACAAGGTTTT[ATTTTA/TTTTTT]TTTTTTTGGTGAGAT	100507650
rs370776483	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23228723	ATCAAGACTACATCA[C/T]TTCAAGACTTATCAT	100507650
rs370782238	in-del	-/TA			intron-variant	RNF212B	GRCh38.p7	14:23218968	AAGAAACAAATAACA[-/TA]AAATAGAGCACCAAT	100507650
rs370815327	in-del	-/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207129	GCTGCTATTTCAGAA[-/G]TACAGCCAACAACAA	100507650
rs370871380	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23233086	CTTCTGCCTTGGGAT[C/G]CTGTTGATCTATGAC	100507650
rs370872985	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198828	ATTTTGGGAGGAAGG[A/G]TTTTCACTATCAGAA	100507650
rs370965789	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23188000	TGAAATGAGGAGACT[C/T]GGTCAGTGATTAAGC	100507650
rs370984330	snp	A/G	0.0279526	0.114869	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208950	TTTTTAGTAGAGACG[A/G]GGTTTCATCGTGTTA	100507650
rs370995694	in-del	-/GT			intron-variant	RNF212B	GRCh38.p7	14:23234298	TGTGCTTTACTTTTC[-/GT]GTGTGTGTGTGTGTG	100507650
rs370996472	snp	A/G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237877	GGAGCCACGCCCACT[A/G/T]ATTTAGCATACCGCC	100507650
rs371010647	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218290	GGAGAATTGCTTGAA[C/T]CTGGGAGGTGGAGGT	100507650
rs371021158	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23243595	CAGCAGCTTGGGAGG[A/C]TGAGGCACGAGAATT	100507650
rs371023359	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23222829	GGCTGAGGCGGGGGG[-/G]ATCATCTGAGGTCAG	100507650
rs371038260	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23269651	TAGGAAGTCAAGGCT[A/G]CAGTGAGCCATGATC	100507650
rs371093389	snp	G/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23250876	CATAGGTAGATAAGA[G/T]ACCAATGGTTGCCTT	100507650
rs371100868	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23233148	GTGCTGTGTCCACTC[A/G]GGGTTAAATGGATTA	100507650
rs371122592	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219950	GCATTTTGGGAAGCC[A/G]AGGCAGGTGGATCGT	100507650
rs371144444	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200072	AGTGTACTATCGTCT[C/T]GAAACATTTTTTTCT	100507650
rs371145434	in-del	-/CT	0.00636936	0.0560724	intron-variant	RNF212B	GRCh38.p7	14:23269763	GCAGGGAATTTTTTC[-/CT]CTCTGGCCTAGCTGT	100507650
rs371196152	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23225741	ATAAGACCTAGTATT[G/T]GATAGCATAACAGGG	100507650
rs371222254	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23188478	TTTTTTTTTTTTTTT[A/T]GAGATAGGGTCTCAC	100507650
rs371282524	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23216157	AGGCTGAGGCAGGAG[A/G]ATGGCGTGAACCTGG	100507650
rs371325887	in-del	-/AAAAC/CA			intron-variant	RNF212B	GRCh38.p7	14:23254292	CTTTATCTCAAAAAC[-/AAAAC/CA]AAAACAAAACAAAAC	100507650
rs371335961	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197240	GTGAGAAAAATATAA[C/T]GAGAGGCCAGGCACT	100507650
rs371340695	in-del	-/A	0.480775	0.0961398	intron-variant	RNF212B	GRCh38.p7	14:23223054	GTGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	100507650
rs371369717	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23230632	GCACTCCAGCCTGGA[C/T]GACAGAGCGAGACTC	100507650
rs371379817	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23261907	GAGGCAGAGCTGGCA[C/G]TAGTGAGCCGAGATC	100507650
rs371487088	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266962	TATTATTGTGGTTTT[C/T]GGTTTTTTGTTTTCT	100507650
rs371490643	snp	C/T	0	0	intron-variant	RNF212B	GRCh38.p7	14:23251649	GGTGAAACCCTGCCT[C/T]TACTAAAAATACCAA	100507650
rs371525483	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23194437	ATTTTAATGTACCTC[C/T]ATTAGAAGCTGATAA	100507650
rs371564067	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23244731	AATTGCTTTGAGTAT[A/G]TAGGCCTGGCCCTGC	100507650
rs371594956	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242493	GTAGGCATAACTGGG[G/T]ACTTTCTTACAGTGC	100507650
rs371650442	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23266539	GCCTCAGCCTCCCGA[A/G]TAGCTGGGATTACAG	100507650
rs371671112	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206544	TATACATTTATAAAG[A/C]CCCTCACCCCCTTTT	100507650
rs371744147	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23256244	TAGGATTAGGATATT[A/T]GGGATACTAACATTG	100507650
rs371764419	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23231731	TCTCGGCTCACTGCA[A/G]CCTCCCTGCCTGATT	100507650
rs371807994	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23233587	AAAAAAAAAAAAATA[A/G]AAAAATTAGCCGGGT	100507650
rs371821803	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23191259	CTACTTGGGAGGCTG[A/G]GGCAGGAGACTCACT	100507650
rs371851418	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197452	GAATTGCTTGAACCC[G/T]GGAGGCGGAGGTTGC	100507650
rs371864211	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23218376	CTATCTCAAAAAAAA[A/T]AATAAATAAAAAGAA	100507650
rs371870911	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23221189	GTCAGGAGTTTGAGA[C/T]GAGCCTGGCCAGCAT	100507650
rs371936043	in-del	-/CAAA			intron-variant	RNF212B	GRCh38.p7	14:23254292	TCTTTATCTCAAAAA[-/CAAA]ACAAAACAAAACAAA	100507650
rs371944416	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267680	GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC	100507650
rs371978828	snp	C/T			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200790	GCTTCTTAAGTCAAG[C/T]TTGATTCCTTATAGG	100507650
rs372017587	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201527	CAAAGAAACCAAATA[A/C]CCATTTCATATTTGA	100507650
rs372031559	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23271334	TGTAATCTCAGCTAC[A/C]TGAGAGGCTGAGACA	100507650
rs372035339	snp	A/G/T			intron-variant	RNF212B	GRCh38.p7	14:23235073	AAAAATTAACCAGGC[A/G/T]TGGTGGCAAATGCCT	100507650
rs372040149	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211318	ACAGGCAAGATGAAT[A/G]GATAACCTAAATATC	100507650
rs372040525	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199907	TCCTAATTAGGAAAC[A/G]TGGGAAAAAAAGAAG	100507650
rs372104920	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23189124	CCTACCACAATCTTG[C/T]AGTTAACTGACCTTT	100507650
rs372177310	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23264608	ATTAATTGATGCTTA[A/T]TATTTGTCTATCAGG	100507650
rs372262124	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205886	GGGTTTATAGTTTTG[G/T]AACTTCTATGCCAAA	100507650
rs372269233	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23222553	CTGAATTCTACCAAA[C/T]ATTTAAAGAACTACT	100507650
rs372310625	in-del	-/AAG	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23187930	GAAAATTAATGAGAA[-/AAG]AAGAAAAAATTAAAA	100507650
rs372395329	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23193450	TAGGATAAGAGGGTG[A/T]ATTAGGACCAGACAG	100507650
rs372404194	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23186214	TTGGAATCTTTTTGT[A/G]ACATAAACTCTTAAG	100507650
rs372416020	snp	A/T			upstream-variant-2KB, intron-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185610	TGCAAACTGATAACG[A/T]TATGGTAAGCTTTAG	100507650
rs372481437	snp	A/G	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23230551	CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA	100507650
rs372491728	snp	A/G	0.0107246	0.0724382	intron-variant	RNF212B	GRCh38.p7	14:23217822	ACTCACCAGTTCTCA[A/G]ACACTGATGAACATC	100507650
rs372505895	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195889	TTCAAAATTATGTGA[C/T]TTGCCAAGGACACAC	100507650
rs372565888	snp	A/G			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274674	GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAT	100507650
rs372570307	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23255692	CAATATAGCAAGATA[C/T]CATTTCTAAAAAAAT	100507650
rs372686414	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23263837	TTATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	100507650
rs372706677	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23194103	CGCCTCGGCCTCCCA[A/G]AGTGCTGGGTTTACA	100507650
rs372762924	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23241526	CTTCCCAGGTTCAAG[C/T]GATTCTCATGTCTCA	100507650
rs372793100	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272351	CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTAAG	100507650
rs372835968	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23186731	ATTTTTTTCCTCCTC[A/G]TGTAGTATCTTGGGC	100507650
rs372899002	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212B	GRCh38.p7	14:23232561	GAGGTGGGGGTCAGC[C/T]CCCGCCCAGCAGCCA	100507650
rs372904453	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23269025	AACTCTGCCAGCAGG[C/T]TGGGTGCGGTGGCTC	100507650
rs372925521	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23191652	GAAGAATAGAGGGAA[A/G]GATAGGTTACCAGTG	100507650
rs372935696	in-del	-/TGCAGTCATT			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213702	TCTACCTAAACAGGG[-/TGCAGTCATT]TGACTGCATGCCAAA	100507650
rs372971261	in-del	-/AAACAAAA			intron-variant	RNF212B	GRCh38.p7	14:23228665	AACAAAAAAACAAAA[-/AAACAAAA]CAAAACAAAACAAAA	100507650
rs372974382	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23257014	AAATATTAGCCAGGC[A/G]TGGTGGCGGACGCCT	100507650
rs373085125	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23228288	TGATAATAAAATTCA[A/T]TTGGAAATGCAAATG	100507650
rs373087865	snp	A/G	0.0501905	0.150254	intron-variant	RNF212B	GRCh38.p7	14:23266437	TTTTTTTGAGATGGT[A/G]TTTCTTTCTTGTTGC	100507650
rs373102506	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23187725	CCATGCGCTCACTCC[A/G]TCCTTCTTCTCGTAA	100507650
rs373109382	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203904	TCTACAGTTTTTTGA[C/T]TTTTTGATTATAGCC	100507650
rs373134150	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23264316	CAAGAACTTAAATTT[A/T]TATTGGTTTTGGCAT	100507650
rs373155457	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23232462	CAGCCGCCCCGTCTG[A/G]GAAGTGAGGAGCCCC	100507650
rs373220927	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23217772	TAAGAAGGACAGGCA[C/G]AAACAAGCCCAGACC	100507650
rs373235696	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23241542	GATTCTCATGTCTCA[A/G]CCACTTGAGTAGCTG	100507650
rs373270267	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23242860	GGTGTGCGCCTGTGG[C/T]CCCAGCTAGTCAGAA	100507650
rs373281606	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208799	AGTCTCACTCTGTCG[C/T]CCAGGCTGGAGTGCA	100507650
rs373463189	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23241899	CCATCCTGCTAACAC[A/G]GTGAAACCCCATCTC	100507650
rs373483515	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195689	CTAATACTCCTCAGT[A/G]GAGATGGGTCCTTGC	100507650
rs373513424	snp	C/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23195171	TGTGGTGCACGTCTA[C/T]AGTCCCAGCTATTTG	100507650
rs373572346	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23269853	TGATGCTTTTATTTG[A/C]TTTCCTTAGAACTTC	100507650
rs373632192	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23251724	TGGAGGCTGAAGCAG[C/G]AGAATCACTTGAACC	100507650
rs373650808	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23220074	CTGTAATCCCAGCTA[C/T]TCCAGAGGCTGAGGC	100507650
rs373706075	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266674	CCTCATCCTCCCAAA[A/G]TGCTGAGATTACAGG	100507650
rs373722607	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184953	TTAATTTTAAAGTGG[A/G]CCTAAAAAATTAAGT	100507650
rs373725003	in-del	-/AACA			intron-variant	RNF212B	GRCh38.p7	14:23261969	GGGACTCTGTCTCAA[-/AACA]AACAAACAAAAAAAC	100507650
rs373771004	in-del	-/AC/C			intron-variant	RNF212B	GRCh38.p7	14:23254291	TCTTTATCTCAAAAA[-/AC/C]CAAAACAAAACAAAA	100507650
rs373813243	in-del	-/AAT			intron-variant	RNF212B	GRCh38.p7	14:23238738	CAGACCCTGTCTCAA[-/AAT]AATAATAATAATAAT	100507650
rs373826935	in-del	-/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237132	CCACACCCGGCTAAT[-/T]TTTTTTTTTTTTTTA	100507650
rs373989893	snp	A/C/T			intron-variant	RNF212B	GRCh38.p7	14:23234901	GGCAACACAGTGAGA[A/C/T]CTTGTCTCTTAAAAA	100507650
rs373994408	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23186616	GCCTCCCAAAGTGCT[A/G]GGATTACTCTATTCT	100507650
rs374067480	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23266981	TTTTTGTTTTCTTGT[G/T]TTTTTGAGACAGAGT	100507650
rs374151408	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244018	AAAAGGCGAGGGTTG[C/T]AATGAGCCTAGATCA	100507650
rs374243903	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273342	TTATACTTTTTTATT[C/T]GTCTATTATTTCCTC	100507650
rs374258494	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23239388	CTGCAGAAGAAAAGT[A/G]TATTTCCTTCTGTGG	100507650
rs374431350	in-del	-/GT			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197589	GCAAATTAAAAATTA[-/GT]TTTAAAAAAACAAAT	100507650
rs374441726	snp	C/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199366	TTGAGATTCTGTTAG[C/T]CTTTCCAAAGGAGGC	100507650
rs374472484	in-del	-/AA			intron-variant	RNF212B	GRCh38.p7	14:23193762	TTAACAAAAAAAAAA[-/AA]GGAAGAATGGAAAGA	100507650
rs374478156	snp	C/T			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270549	CACAAGTAACACTGC[C/T]GAGAAACTGCCCAAG	100507650
rs374486202	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23193246	TACATAGCCAAAGTA[G/T]CAATCAAAAGTGGGT	100507650
rs374552073	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23217256	AGTGGTGGCAGTGGT[-/G]GGGGGGGGGCTCCTC	100507650
rs374607127	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23230546	GTAGTCCCAGCTACT[C/T]GGGAAGCTGAGGCAG	100507650
rs374729877	in-del	-/AACAAC	0.0178098	0.0926698	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236519	GACTCTGCTTCAAAA[-/AACAAC]AACAACAACAACAAA	100507650
rs374760688	snp	A/C			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214220	AAACTAAGGCTGGGC[A/C]TGGCGGCTCAAGCCT	100507650
rs374765420	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23217711	AAAAATCACAGTATT[A/G]CAGGGCTTGGGACCC	100507650
rs374813233	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23225081	GATGCCACCCCACAC[-/A]AAAAAAAAAACACCT	100507650
rs374821243	in-del	-/CACGCCCCGCG	0.0115144	0.0749975	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237843	TCTGCGGGCCCCGCC[-/CACGCCCCGCG]CACGCCACGGAGCCA	100507650
rs374871650	in-del	-/AT	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23218967	AAAGAAACAAATAAC[-/AT]AAAATAGAGCACCAA	100507650
rs374881696	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23242733	AACTCACCACTTTGC[C/G]GGGGCCAAGGTGGGA	100507650
rs374887186	in-del	-/CAA			intron-variant	RNF212B	GRCh38.p7	14:23254292	TCTTTATCTCAAAAA[-/CAA]AACAAAACAAAACAA	100507650
rs374949776	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209337	CTATCTCATCCTGTG[A/T]CTTAGAATGCCTTAA	100507650
rs374961173	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196958	ATTAATGTCTACCTC[C/T]CCATCTAGACTGCAA	100507650
rs374985131	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259953	TCTAAAGGTGAATGA[A/G]ATAGATTTTCCTTAT	100507650
rs374991698	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244824	ATTTCTTGTTTCCCA[C/T]TCTCACTTTTCAATA	100507650
rs374997087	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23227945	TAAAAATCTCATCAG[A/G]CAATGCCAGGCATGG	100507650
rs375013845	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23229220	TGGCTGAATAATATT[A/T]TATATATATATATAT	100507650
rs375036468	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221834	ATCAATAACAGGAGG[A/G]ATTTTGGAAAGTATA	100507650
rs375043194	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223591	CGATCTCCTGACCCC[A/G]TGATCTGCCCGCCTC	100507650
rs375058539	in-del	-/GAA			intron-variant	RNF212B	GRCh38.p7	14:23228693	AAAACACAAGAAGAA[-/GAA]AGAACAAAGAGGATC	100507650
rs375060458	in-del	-/C			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236961	TTATTCTGTCTCTCT[-/C]TTTTTTTTTTTTTTT	100507650
rs375079732	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23263409	CACAATCTAGAAATG[G/T]AACCACTGCTCTTTT	100507650
rs375108847	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23188294	AAGAGGCACTGCCTG[C/T]GGCAGGCCAGATCTC	100507650
rs375158145	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196425	CCTCAGATGACCTAC[C/T]AAAGGGCTCAAAAAA	100507650
rs375323219	in-del	-/C	0.0119091	0.0762411	intron-variant	RNF212B	GRCh38.p7	14:23250444	GCCTAGAATGTGCCA[-/C]TGCACTCCAGCCTGG	100507650
rs375358772	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23269568	GAGACCTAATTACCC[A/G]GGCTTGGTGGGTGTA	100507650
rs375392632	snp	C/T	0.0252325	0.109451	intron-variant	RNF212B	GRCh38.p7	14:23219958	GGAAGCCGAGGCAGG[C/T]GGATCGTTTGACGTC	100507650
rs375425335	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23233114	GACCTTACCCCCAAC[C/T]CTGTGCTCTCTGAAA	100507650
rs375501649	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23244466	TCTTATTCCTTTATC[-/A]AAGGTTTTCTTTAAA	100507650
rs375580669	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221829	TAAAAATCAATAACA[A/G]GAGGAATTTTGGAAA	100507650
rs375581689	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213034	AATTATAACACAGGC[C/T]GGGCATGGTGGGTTA	100507650
rs375627805	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23228833	ATGGGCTTGAATATG[C/T]ATAGAACACTGATTT	100507650
rs375635394	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23261585	AAGTGCCTACTGTTT[A/G]TCAGGTACCATGTTA	100507650
rs375635832	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272702	TGCAATGAAGAAAAC[C/T]ATGGGGAAGCAAAAG	100507650
rs375637447	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23254058	CCGAAGTGGGAGAAC[A/G]GCTAGATCCCAGGAG	100507650
rs375664686	in-del	-/TCCCC	0.0718919	0.175435	intron-variant	RNF212B	GRCh38.p7	14:23226739	TCTTATCTCGGCTAG[-/TCCCC]TCCCCTCCCCTCCCC	100507650
rs375684797	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236382	TAGCTGGGCGTAATG[G/T]CAGGCGCCTGTAATC	100507650
rs375793720	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193993	ATTACAGGAGCCTGC[C/T]GCTACGCCTGGCTAA	100507650
rs375794555	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23258926	TGCAGTGGCTCACAC[C/T]TGTAATCCCAGCACT	100507650
rs375821816	snp	A/C/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259366	GCTAATTTTTGTATT[A/C/T]TTTTTTTTTTTTTGT	100507650
rs375880115	in-del	-/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201808	TTATTGAGAGAGGGG[-/G]ACTTAATTTTCTAAA	100507650
rs375917225	in-del	-/TTTTTC			intron-variant	RNF212B	GRCh38.p7	14:23239610	AGGATTGTATTTTCT[-/TTTTTC]TTTTTCTTTTTCTTT	100507650
rs376169343	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208599	GTTACAGGAAAGGGG[C/T]CCAGACCCAGACCCC	100507650
rs376184675	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208758	GGCTGCTGGTTGCCG[G/T]TTTTTTTTTTTTTTT	100507650
rs376186922	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23186174	TCAAAGGGAGCATTA[C/T]TTATATTAAGTGCCT	100507650
rs376196632	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208441	GTTCAAGACTGCAAT[G/T]AGCTATGATCACACT	100507650
rs376234879	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208894	CCCCTGAGTAGTTGG[A/G]ACTACAGGTGCCCGC	100507650
rs376257168	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266441	TTTGAGATGGTGTTT[C/T]TTTCTTGTTGCCCAG	100507650
rs376324706	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23187982	GTCAGAAAGAAAGGA[A/G]GATGAAATGAGGAGA	100507650
rs376326530	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220418	ACACCTGTAGTTCCA[G/T]CTACTTGGGAGGCTG	100507650
rs376338170	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23192242	ACATGCACATGTATG[C/T]TTATTGCGGCACTAT	100507650
rs376393311	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23269108	TCAGGAGTTTGAGAC[C/T]AGTATGGCCAACATG	100507650
rs376413079	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23216289	CAAAATCTATACAAG[A/G]TGATACATTCCAAAA	100507650
rs376437372	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23243047	TGTGAAAGCCCTACT[G/T]ATATCTCAACATATT	100507650
rs376437680	snp	C/T	0.0640965	0.167152	intron-variant	RNF212B	GRCh38.p7	14:23231909	GGCCTCCCGAGGTGC[C/T]GGGATTGCAGACGGA	100507650
rs376451658	in-del	-/ACAA			intron-variant	RNF212B	GRCh38.p7	14:23272448	CAAACAAACAAACAA[-/ACAA]CCGAAAATGTGAAAA	100507650
rs376453351	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242119	AAAAGAAAAGAAAAA[A/G]AAAAAGAAAAACCTT	100507650
rs376458688	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23271013	GGGTACTACTTGAAC[C/T]AGGAAAAACCACATT	100507650
rs376462567	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23242468	CAAATATTAGCAAAG[G/T]GATGACAAGGTAGGC	100507650
rs376510516	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203279	ACTTACAATAATAGT[C/T]TCCAATCTCATCTAC	100507650
rs376565489	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23186360	CATTTTTTTTTTTTT[G/T]GAGAAGGAGTCTCGC	100507650
rs376571740	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23235880	ATTTTAATGTAACCG[A/G]CTATAAAAAGTTCAT	100507650
rs376600844	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23234038	GGAGGCAGAGGTTGC[A/G]GTGAGCTGAGATAGT	100507650
rs376636901	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23250029	ACCTCTCCAATTTCA[A/G]TCACAACTACCATCT	100507650
rs376648717	in-del	-/AAAA			intron-variant	RNF212B	GRCh38.p7	14:23251815	TGAGACTCTGTCTCA[-/AAAA]AAAAAAAAAAGAAAG	100507650
rs376655448	in-del	-/CAAA			intron-variant	RNF212B	GRCh38.p7	14:23261979	CTCAAAACAAACAAA[-/CAAA]AAAACAGAAAACAAA	100507650
rs376675146	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23216021	GAGGCCAAGGCGGGC[A/G]GATCACGAGATCAGG	100507650
rs376735597	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203542	GGAGTGCAATGGCAC[A/G]ATCTTGGCTCACTGC	100507650
rs376844366	in-del	-/CTGT	0.247053	0.249983	intron-variant	RNF212B	GRCh38.p7	14:23232335	CTCTGCCCGGCTGCC[-/CTGT]CTGAGAAGTGAGGAG	100507650
rs376876200	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23229352	GGTAGGAATATTGGT[G/T]TACACATATCTGTTT	100507650
rs376916417	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23266380	TATTGATTTTGACTT[G/T]CAGTGATTTAAATCC	100507650
rs376924239	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23233120	ACCCCCAACTCTGTG[A/C]TCTCTGAAACATGTG	100507650
rs376940058	in-del	-/TGATGTCACTCCTAGCTAATTTTTGT			intron-variant	RNF212B	GRCh38.p7	14:23268626	CTAGCTAATTTTTGT[-/TGATGTCACTCCTAGCTAATTTTTGT]CTTTACCCATTCTTT	100507650
rs377068519	snp	A/G	0.0182019	0.0936463	intron-variant	RNF212B	GRCh38.p7	14:23230586	GTGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	100507650
rs377083748	snp	C/T	0.107806	0.205623	intron-variant	RNF212B	GRCh38.p7	14:23243320	TAATGTAAGTTTTTC[C/T]CCCCCTGCCACAAAC	100507650
rs377144831	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200086	TTGAAACATTTTTTT[C/T]TCTCTCTCTCTAGTT	100507650
rs377178798	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23187543	AGAGACAAGTTAGAC[A/G]TGTCTGCTAATGCAA	100507650
rs377199145	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253116	AAAACCAAATATTAC[A/G]TCATTTCTATCTGTA	100507650
rs377240022	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197860	AGAGAGTCAGCGAAG[G/T]GAGATAGGGGTGGGG	100507650
rs377270840	snp	C/T			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274678	TTTGGGAGGCCAAGG[C/T]GGGCGGATCATGAGG	100507650
rs377274855	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206679	CAGGTGAAAATCAAA[C/T]AGCAAAATTTACATC	100507650
rs377275668	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23240267	GAAGCTAAGCAAGCA[C/T]GGTTACATAGATTTT	100507650
rs377283447	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198767	ATAGTTCTCAAACGG[C/G]TTTACATATGTACTG	100507650
rs377336643	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197990	GGGGGAGATTACAAA[G/T]TACATTGATCAGTTA	100507650
rs377385875	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213188	CGTGGTGGCAGGCGC[C/T]TGTAGTCCCAGCTAC	100507650
rs377386921	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23262433	TTAAAACTTCTATTA[C/T]GGGCAACACAGAGGT	100507650
rs377398834	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203721	GACCTCATGTGATCC[A/G]CCTGCCTTGGCCTCC	100507650
rs377443676	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201922	AGTATAAAATATAAC[C/T]TCCATAAACCTTTTA	100507650
rs377449781	in-del	G/TT			intron-variant	RNF212B	GRCh38.p7	14:23242216	TCATGACCTTTTAAA[G/TT]TTCGCTAATGTAAAA	100507650
rs377470793	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198106	GCCATCTGGATGTGT[A/C]CGTGCAAGTCACAGG	100507650
rs377518819	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195290	AAAACCCATGAGATG[A/C]AGCTAAAGTAGTATT	100507650
rs377525826	in-del	-/CAA			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206956	GAAAAACAACAACAA[-/CAA]ACAAAAACATGAAGG	100507650
rs377531515	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23261458	AAAGTCTTTAAAGAG[G/T]AACCTCCACCTTACT	100507650
rs377553934	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23221449	GAGAGTGTAACAATT[G/T]TAAGTATATATGCAC	100507650
rs377555908	in-del	-/AC			intron-variant	RNF212B	GRCh38.p7	14:23238420	TATCCCTCAGCGGTT[-/AC]ACACACACACACATC	100507650
rs377572896	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211975	TCAAGTTATCTGCCC[C/T]CCTCAGCCTCCCAAA	100507650
rs377694199	snp	A/G	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23253876	ATCGTGAATTTACCA[A/G]TATCTTTAAAGTGAA	100507650
rs386380887	in-del	-/AA			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214647	GAATAAAGCATAGGA[-/AA]AAGTCAGTGAACTTG	100507650
rs386380888	in-del	-/AA			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214648	AATAAAGCATAGGAA[-/AA]AGTCAGTGAACTTGA	100507650
rs386380890	in-del	-/AAAA			intron-variant	RNF212B	GRCh38.p7	14:23251822	CTGTCTCAAAAAAAA[-/AAAA]AAAGAAAGAAAGAAA	100507650
rs386380891	in-del	-/TTC			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260270	ATACCTCAGGACCCT[-/TTC]TCCTCTGCATCACAC	100507650
rs386775591	in-del	CT/TCCTTGTTTG			intron-variant	RNF212B	GRCh38.p7	14:23191467	TTGTTCCTTGTTTGT[CT/TCCTTGTTTG]TTCCTATTAAAATGT	100507650
rs386775592	multinucleotide-polymorphism	CG/GA			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209624	TAAATAATATATGTA[CG/GA]TACTTTTTCTTGCAG	100507650
rs386775593	multinucleotide-polymorphism	CGGGCGTGGTGGCA/TGGGCGTAGTGGCG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213169	ATACAAAAAATTAGC[CGGGCGTGGTGGCA/TGGGCGTAGTGGCG]GGCGCCTGTAGTCCC	100507650
rs386775594	multinucleotide-polymorphism	AT/TC			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213482	AAATTCCACCAGGAG[AT/TC]ATGAGGCGGAAAGAA	100507650
rs386775595	in-del	AGTCATT/TCTACCTAAACAGGG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213688	TTAGGAACTGTGTGC[AGTCATT/TCTACCTAAACAGGG]TGACTGCATGCCAAA	100507650
rs386775596	multinucleotide-polymorphism	CA/TG			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214221	AACTAAGGCTGGGCA[CA/TG]GCGGCTCAAGCCTGT	100507650
rs386775597	multinucleotide-polymorphism	AG/GT			intron-variant	RNF212B	GRCh38.p7	14:23216924	AATCTCAAAGGTTAC[AG/GT]ATTGTATGATTCCAC	100507650
rs386775598	multinucleotide-polymorphism	CTG/TTT			intron-variant	RNF212B	GRCh38.p7	14:23219556	GGCTCACTGCAACCT[CTG/TTT]CCACCTGGGTTCAAG	100507650
rs386775599	multinucleotide-polymorphism	ACA/CCG			intron-variant	RNF212B	GRCh38.p7	14:23227857	ACCCACCTCAGCCCC[ACA/CCG]AAGTGCTGGGATTAC	100507650
rs386775600	multinucleotide-polymorphism	AGT/TGC			intron-variant	RNF212B	GRCh38.p7	14:23251644	AACATGGTGAAACCC[AGT/TGC]CTCTACTAAAAATAC	100507650
rs386775601	multinucleotide-polymorphism	AT/GC			intron-variant	RNF212B	GRCh38.p7	14:23262882	CCAGGCAAGGCAGGC[AT/GC]ACCATTGATGGCAAC	100507650
rs397715313	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23263101	TAGGGTTTTTTTTTT[-/T]TCCCTAAGCCAAACT	100507650
rs397722108	in-del	-/AAC			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209764	ACTCTCTTAAACAAC[-/AAC]TCAAAATTAATATCA	100507650
rs397736578	in-del	-/T/TG			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259452	TTTAAAGTTTTTTTT[-/T/TG]GTTTTTTTTTTTTAT	100507650
rs397758209	in-del	-/A	0	0	intron-variant	RNF212B	GRCh38.p7	14:23233418	TAAAAAAAAAAAAAA[-/A]GAATATTTAAAGAAA	100507650
rs397776598	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23247154	CAAAAAAAAAAAAAA[-/A]TTGTTTTCAAGGGGA	100507650
rs397782567	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23242218	TGACCTTTTAAAGTT[-/T]CGCTAATGTAAAAAG	100507650
rs397786830	in-del	-/T	0	0	intron-variant	RNF212B	GRCh38.p7	14:23256389	AATTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC	100507650
rs397796741	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23223373	TTCCTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC	100507650
rs397806511	in-del	-/A			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185273	CAACAACAAAAAAAA[-/A]CCAGACAAGGCAGGG	100507650
rs397813654	in-del	-/TTC			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260272	ACCTCAGGACCCTTC[-/TTC]CTCTGCATCACACTC	100507650
rs397814674	in-del	-/A			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185251	TCAGCAAAAAAAAAA[-/A]CAACAAACAACAACA	100507650
rs397852137	in-del	-/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205327	ACCCTTTTTTTTTTT[-/T]AAGCAAGAATGTTTT	100507650
rs397852462	in-del	-/C			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23216073	ACACGGTGAAACCCC[-/C]ATCTCTACTAAAAAT	100507650
rs397852731	in-del	-/AC			intron-variant	RNF212B	GRCh38.p7	14:23240017	CACACACACACACAC[-/AC]TCATAACCTCACCAC	100507650
rs397852993	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23264835	TTTTTTTTTTTTTTT[-/T]GGTGAGATGGAGATT	100507650
rs397853055	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23250497	AAAAAAAAAAAAAAA[-/A]GACTGAATTAATAAT	100507650
rs397853082	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23238271	TTTCAGTGGTTTTTT[-/T]AGACTCACTTGCTGG	100507650
rs397853469	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23233584	AAAAAAAAAAAAAAA[-/A]TAGAAAAATTAGCCG	100507650
rs397941758	in-del	-/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209313	TATGACCTGTATTTT[-/T]GTGCTGACCTATCTC	100507650
rs397974467	in-del	-/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259465	TTGTTTTTTTTTTTT[-/T]ATGGAATGCTTCAAG	100507650
rs398024550	in-del	-/A	0	0	intron-variant	RNF212B	GRCh38.p7	14:23193763	TAACAAAAAAAAAAA[-/A]GGAAGAATGGAAAGA	100507650
rs398024551	in-del	-/A	0	0	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202268	AAAAAAAAAAAAAAA[-/A]GCAGTTGGTTAATGC	100507650
rs398024552	in-del	-/A/T	0	0	intron-variant	RNF212B	GRCh38.p7	14:23226826	CTTTTTTTTTTTTTT[-/A/T]AATAGAGAGGAGGTC	100507650
rs398024553	in-del	-/AA	0	0	intron-variant	RNF212B	GRCh38.p7	14:23240047	TCAAAAAAAAAAAAA[-/AA]TCTCACCACTGTCTG	100507650
rs398043702	in-del	-/A	0.5	0	intron-variant	RNF212B	GRCh38.p7	14:23226297	GCAAGAAACCGTCTC[-/A]AAAAAAAAAAAAAAA	100507650
rs398056931	in-del	-/AA			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195277	TAAAGAAAAAAAAAA[-/AA]CCCATGAGATGCAGC	100507650
rs398077631	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23186359	GCATTTTTTTTTTTT[-/T]TGAGAAGGAGTCTCG	100507650
rs527262473	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213530	TCATCCACATTCTCC[C/T]GTCCCTCTGGGTATC	100507650
rs527263575	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23233500	GGAGGCTGAGGTGGG[A/G]GGATCAGTTGAGCCC	100507650
rs527288276	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211861	CCAAGTAGCGAGGAC[C/T]ACAGGCACATGCCAC	100507650
rs527295254	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191793	GCTTGTTTCTTCACC[A/G]TTATTTACCTAAGGC	100507650
rs527343885	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232933	CTCATTGAGAACGGG[C/G]CATGATGACGATGGT	100507650
rs527356938	in-del	-/AGAG	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23230162	ATGGTGGAAAAAGGA[-/AGAG]AGAGAGAGTTGTAGT	100507650
rs527362447	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185249	GACTCAGCAAAAAAA[A/C]AACAACAAACAACAA	100507650
rs527371353	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23267397	TCTTGATAAATGGAC[A/C]CCTTTATCATTATTT	100507650
rs527425264	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192820	TTTATGGCCAGGTGC[A/G]GTGGCTCATGCCTGT	100507650
rs527449932	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23261081	TTACTGCTGTGTCCG[G/T]TTTCCATTGGCTGGA	100507650
rs527482430	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223332	CCACAGCTAATATTA[C/T]ACTGAATGGAGAAAA	100507650
rs527514246	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23185977	TGGTGGCTCACGCCT[A/G]TAATCCCAGCTACTC	100507650
rs527517671	snp	A/T	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23259029	TCTAAAAAAAAAAAA[A/T]TTTTAAACAAAAATT	100507650
rs527616872	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23187846	TCACTGCCTATGGTC[A/G]ATTAGATGGGGCCTT	100507650
rs527620055	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218323	CAGTGAGCCAAGATT[G/T]CACCTCTGCACTATA	100507650
rs527672633	in-del	-/AAAA			intron-variant	RNF212B	GRCh38.p7	14:23230680	AAAAAAAAAAAAAAA[-/AAAA]CCATTGCCAAATACA	100507650
rs527672932	in-del	-/AG	0.00358779	0.0422022	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208708	AAGTAAAGGAATAAA[-/AG]AGAATGGCTACTTCA	100507650
rs527684392	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221720	TGGGTAATTCTTAAG[A/G]ATAGACGATATGTTA	100507650
rs527691583	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265635	TTATTTCTGTCAGGT[A/T]GGTAACAACAGTGTT	100507650
rs527701907	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183619	CTACTGCACAGCCGG[C/T]CCCATCCCTCTGGTT	100507650
rs527765770	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251952	CCTCCAAGTGTTCAC[C/T]AACTTGGTAACTCTC	100507650
rs527767162	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259264	CACTGATAACACTCA[C/T]TGTAGCCTCAATCTC	100507650
rs527816376	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216520	CAGAACAGATTAAAA[A/G]ACAAACATGACCGAG	100507650
rs527840390	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246599	AGTACTTTAAAAAAA[A/G]ACAAACAAAAAACAG	100507650
rs527865619	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23227084	GGTACCAATGTCAAT[G/T]TATTGGTTTTGATAT	100507650
rs527946394	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23271416	CCACTGCACTCCAGC[C/T]TGGGCAGCAGAGTGA	100507650
rs527946903	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23198982	CACACAAATATTACC[C/T]AGTGCTATACCTCAC	100507650
rs527986891	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23239128	GAGTGCAGTGGCACG[A/T]TCTTGGCTCACTGCA	100507650
rs528008095	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206369	TGAGCCACCGTGCCC[A/G]GCCTAGTCTTTTCTT	100507650
rs528056534	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255488	ATCAATGTTCCAATA[A/C]AACAAACAATATTTA	100507650
rs528145368	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214512	AATAATTAAATTAAA[C/T]TAAAATTTTAAAATT	100507650
rs528153296	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256251	AGGATATTTGGGATA[C/T]TAACATTGTGATTTG	100507650
rs528174784	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23248958	CTGCTACCCAACTCT[A/G]CTGTTGTAGCATGGA	100507650
rs528179687	snp	C/T			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274655	GCTCATGCCTATAAT[C/T]CCAGCACTTTGGGAG	100507650
rs528185678	in-del	-/AAAAACAAAAAC	0.247627	0.249989	intron-variant	RNF212B	GRCh38.p7	14:23220192	TGTCTCGGGAAAAAC[-/AAAAACAAAAAC]AAAAACAAAAACAAA	100507650
rs528249518	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243069	CAACATATTAGTTTG[A/G]AAACACTTGTTTAGA	100507650
rs528300314	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23223639	GGATTACAGGCGTGA[A/G]CCACCGCGCCCGGCC	100507650
rs528301078	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204453	ACCTGTGGCTAGCCA[A/G]TTATCCCAGCGCCAT	100507650
rs528420840	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23222305	AGAAGAAAAAGGAGA[C/T]ATAACTAATACCACA	100507650
rs528424377	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240679	AGGACTAGAATGTAC[G/T]CGTTAGTGTTTTGAA	100507650
rs528484047	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213335	AAAAAAATTATAAAA[C/T]GTTACTGAGAGAAAT	100507650
rs528503761	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208458	GCTATGATCACACTG[C/T]ACTCTAGAATGGGTG	100507650
rs528579722	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201000	TCCAAATTTTGTTCA[C/T]GGGAGTATACTAAAT	100507650
rs528580294	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241467	CTCACTTCGTCACCC[A/G]GGCTGGAATGCAGTG	100507650
rs528621871	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202936	GGAGTTAAAGCCCTC[C/T]AACTCAATGTTACAA	100507650
rs528625226	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23238153	CCTCAGGGTCGCCTT[A/G]ATCACCCTGTTCACT	100507650
rs528641744	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187008	ACTTATCTGCTCAGT[A/G]AGACCCACAGGACTT	100507650
rs528668357	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230716	GTCATGAAGATTTTC[C/T]CCTATATTTTCTTCT	100507650
rs528794911	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269557	AGCAACAAAGTGAGA[C/G]CTAATTACCCGGGCT	100507650
rs528795089	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198545	GCTGGGCGTGGTGGC[A/G]GGTACCTGTAATCCC	100507650
rs528804960	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231389	TTTTAAAAAAATGGT[A/G]CTGAAACAATTGGAT	100507650
rs528814592	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223646	AGGCGTGAGCCACCG[C/T]GCCCGGCCAAGCCTT	100507650
rs528825552	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23223857	TAAAGACTCCACCAA[A/C]AACTATTAGAATTGA	100507650
rs528852181	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23239903	GGATTACAGGCGTGA[A/G]CCACTGTGCTTGGCC	100507650
rs528858925	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223635	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	100507650
rs528864409	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246470	CTAACTTATAGCTTT[A/C]TTTCTTTGAACCAGT	100507650
rs528880425	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186900	ATGCTATAGCTACTG[A/G]TCAAAGCCTCAATTT	100507650
rs528996282	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23243124	TTTATAACACAATGA[C/T]ATTCTAAATTCAGTT	100507650
rs529026062	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267078	GGCTTAAGCGATAGT[C/T]CCACTTCAGCCTCCT	100507650
rs529048343	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208947	GTATTTTTAGTAGAG[A/G]CGGGGTTTCATCGTG	100507650
rs529140295	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23248579	CCTGAGTAGCTGGGA[C/T]TACGGGCATGCGCCA	100507650
rs529181313	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208999	TCCTGACCTCGTGAT[A/C]CGCCCGCCTTGGCCT	100507650
rs529202109	snp	C/G	0.0217236	0.101931	intron-variant	RNF212B	GRCh38.p7	14:23242221	ACCTTTTAAAGTTCG[C/G]TAATGTAAAAAGCTG	100507650
rs529228140	snp	C/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185039	CCAAAAGATTTTGGG[C/T]TTTAAGGAAAATAAA	100507650
rs529259327	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203523	TTGCTCTGTCACCCA[C/T]GCTGGAGTGCAATGG	100507650
rs529287167	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253430	CACAGTGTGGATTTT[G/T]TTTATTGTACCTATG	100507650
rs529334561	snp	C/T	0.00199481	0.0315187	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199856	TTAGTCTCAGTTAGC[C/T]GGGCTTTAAGAAAGC	100507650
rs529433615	snp	C/G	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213046	GGCCGGGCATGGTGG[C/G]TTATGCCTGTAATCC	100507650
rs529437754	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207639	GATTTGTCAAAGGTC[A/G]GGGGCAACTCCACTC	100507650
rs529445537	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23264252	AAGTAATGTTCACCT[C/T]ATCTTTCCAGATTGA	100507650
rs529570452	in-del	-/T	0.00716266	0.059414	intron-variant	RNF212B	GRCh38.p7	14:23224490	AGGATGCCAACAACG[-/T]TACACTGGGGAAAAG	100507650
rs529595887	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251143	AAGTGTTCAGTAAAG[G/T]TTTGCTAAATGGAAA	100507650
rs529614496	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229991	GAATCTTCTCCAATG[G/T]CTCCTTTTAAAGTTG	100507650
rs529614506	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235019	GAGTTTGAGACCAGC[C/T]TGGCCAACATGGTGA	100507650
rs529632881	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23193660	AAATGAAAACATGAG[A/G]CAAGTATTAACTTCA	100507650
rs529684301	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215821	AGTAAAAACATGGGT[A/G]AATGTTGACTATCCT	100507650
rs529705049	snp	A/G	0	0	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209993	CCCTGTCTCTGTTAA[A/G]AATACAAAAATTAGC	100507650
rs529735752	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210155	ACTGTCTCAAAACAC[G/T]AACAAACAAAATAAA	100507650
rs529748247	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23223556	GAGACGGGGTTACAC[A/G]ATGTTAGCCAGGATG	100507650
rs529753844	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244660	TAATTTCTACGACTA[A/C]AGGTTGTTTTAGGGA	100507650
rs529806815	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237214	GGCTCACTGCAACCT[C/T]CGCCTTCCGGGTTCA	100507650
rs529836053	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23232400	AGTGAGGATCCCCTC[C/T]GCCCGGCAGCCGCCC	100507650
rs529854269	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197398	CATGTGTGGTGGTAC[A/T]TGCCTGTAGTCCCAG	100507650
rs529870339	in-del	-/GT	0.00636936	0.0560724	intron-variant	RNF212B	GRCh38.p7	14:23247780	TTTTATTCCTCTTGG[-/GT]ATATACCTACGAGTG	100507650
rs529882120	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23239548	ACCATATCACAGGAA[G/T]TAGTTAAAAAAGAAA	100507650
rs529920746	in-del	-/GGT			intron-variant	RNF212B	GRCh38.p7	14:23261534	GTGAAGACTGCATTA[-/GGT]GGAGTTAGATGGTCT	100507650
rs529964092	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273579	AAAAGGCAGAAATGA[C/T]GAATTAAATAGGTTA	100507650
rs529976111	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23227733	ACCTCCTTAGTAGCT[G/T]GGACTACAGGCATGC	100507650
rs529989255	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190057	TTATTGATCTTACGG[A/C]AGCATGTGGCCAGCT	100507650
rs529993056	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265001	TAATTCTGTATTTTT[A/G]GTAGAGACGGGGTTT	100507650
rs530020452	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23232787	CTGGGAGGGAGGTGG[A/G]GGGGGGGTCAGCCTC	100507650
rs530022658	snp	A/G	0.0123036	0.0774623	intron-variant	RNF212B	GRCh38.p7	14:23231744	CAACCTCCCTGCCTG[A/G]TTCTCCTGCCTCAGC	100507650
rs530027501	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232640	CCCGTCCGGGAGGGA[A/G]TTGGGGGGTCAGCCC	100507650
rs530065901	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23242852	GAGGTGGTGGTGTGC[A/G]CCTGTGGTCCCAGCT	100507650
rs530139936	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23219699	CTGGTCTCAAACTGC[C/T]GACCTCAGGTGATCT	100507650
rs530158715	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23235886	ATGTAACCGGCTATA[A/G]AAAGTTCATTGATAT	100507650
rs530195366	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23256530	GTGCACGCCACCATG[C/G]CTGGCTAATTTTTGC	100507650
rs530196361	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23264019	CTTGAACCCAGGATG[C/T]GGAGGCTGCAGTGAG	100507650
rs530284841	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215277	TGAGTCCTCCCTAGC[C/T]GTGCAGAACTGTGAG	100507650
rs530292382	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23219996	CGAGACCAGCCTAGC[A/C]AACATGGTGAAACTC	100507650
rs530324747	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23272714	AACTATGGGGAAGCA[A/G]AAGCAGTGGTGTCTG	100507650
rs530326138	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23190525	CAATCCCTGTTAGCT[A/G]TAGCTTCAAATCAAA	100507650
rs530342867	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23220547	AAAAAACAAAACAGC[C/T]GGGCTCGGTGGCTCA	100507650
rs530402950	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23261822	AAAACAAAATTAGCC[A/G]GGCGTGGTGGAGGAC	100507650
rs530497872	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249854	TTTTAGGGTTCTTTT[C/T]TCCTCAAATCTGTTC	100507650
rs530508694	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214674	CTTGAAGATAAAATA[A/G]TAATAATAATAATCA	100507650
rs530522036	in-del	-/T	0.389527	0.207442	intron-variant	RNF212B	GRCh38.p7	14:23188460	TGACAAAGATTAGGG[-/T]TTTTTTTTTTTTTTT	100507650
rs530532627	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23186883	CTGAGCACTTTTTCA[A/G]GATGCTATAGCTACT	100507650
rs530585087	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209918	AGCACTTTGGGAGGC[C/T]GAGGTGGGCTGATCA	100507650
rs530589880	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203228	ACAGATCAGTGAGAA[C/T]ATATGATGTTTGGTT	100507650
rs530665095	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23243801	TAAATAACAGGCCAG[C/T]TGAGGAGGCTCACAC	100507650
rs530728170	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23221085	CACAATGATCTGTCA[A/C]CTAGAAGAAATACAC	100507650
rs530735758	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242031	AGCTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC	100507650
rs530751549	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196723	CTGGGATTACAGGCA[C/T]GAGCCACTGTTCTAG	100507650
rs530778561	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23217208	GTTAACATCAGCAGT[A/G]GCCTGGCAGAACCAC	100507650
rs530778650	snp	C/T	0.00914312	0.0669923	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237901	TACCGCCAGGCCCCG[C/T]CCACACCTCTCACAC	100507650
rs530820297	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208978	TTAGCCGGGATGGTC[A/T]CGATCTCCTGACCTC	100507650
rs530829752	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237743	CCCCAATCTTTTAAG[C/T]GAGGTGAATTTTCCT	100507650
rs530856480	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248739	GCCATCACGCCCGGC[C/T]CCCAAGCCTCTTTTT	100507650
rs530917110	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23224706	GGGCAAAAATTTCTT[C/G]TGTAATACCCCACAA	100507650
rs530957228	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202035	GTGGGTGGACTGCTT[A/G]AGGTCCGGAGTTCGA	100507650
rs530992042	in-del	-/AAAAAC	0.460194	0.135346	intron-variant	RNF212B	GRCh38.p7	14:23220198	GGGAAAAACAAAAAC[-/AAAAAC]AAAAACAAAAACAAA	100507650
rs531035271	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208944	TTTGTATTTTTAGTA[G/T]AGACGGGGTTTCATC	100507650
rs531079241	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23188878	ACTCAATAAATATGA[C/T]TGATTGAATGAATTA	100507650
rs531108991	snp	A/C	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23263532	CGGCTTAAGGGAGTT[A/C]AGTTTATGCTGAAAG	100507650
rs531113647	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23224352	TCTGACTTCAAATTA[C/T]ACTGCAGAGCTAAAG	100507650
rs531141117	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23271681	TAAGAGGCAACACTG[C/G]GGAAGTAACATTCCT	100507650
rs531142432	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23188067	ATTCATAAGTTCAAA[G/T]GAAGTTGTGTCTTCT	100507650
rs531155827	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23270911	TAAACTGAGAGGTCT[C/T]GGCCAGCGTGAAGTA	100507650
rs531160767	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23189937	CACATCAAAGCTTTT[A/G]TCCCCATCACCTTGT	100507650
rs531171629	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232722	CCGGCCAGCCGCCCC[G/T]TCCGGGAGGGAGGTG	100507650
rs531175460	snp	A/C	0.0123036	0.0774623	intron-variant	RNF212B	GRCh38.p7	14:23231732	CTCGGCTCACTGCAA[A/C]CTCCCTGCCTGATTC	100507650
rs531210431	snp	A/T	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198395	AAAAGGTCCACATAC[A/T]GGAGCCAAGCGTGGT	100507650
rs531260815	snp	C/G	0.00119737	0.0244387	utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23193350	GAGAATGTGCACCAC[C/G]AAAATAAGGGAATAA	100507650
rs531301076	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23239020	AAATGTTGGGACTGA[A/G]CAAACATTAAGTAAT	100507650
rs531308212	snp	C/T	0.170084	0.236883	intron-variant	RNF212B	GRCh38.p7	14:23232895	GCCCGGCCACCACCC[C/T]ATCTGGGAGGTGTAC	100507650
rs531384814	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246496	CCAGTCATACTTCCT[C/T]ACATGTAATATGAAA	100507650
rs531409886	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266545	GCCTCCCGAGTAGCT[G/T]GGATTACAGGCATGC	100507650
rs531423676	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23188353	CAATCTGTCATGGGG[C/T]CTTAACAGTCTTCTT	100507650
rs531427227	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215193	TTCCCCCCACCCCTC[C/T]GCCTCTCCTGTTGTC	100507650
rs531464016	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213961	CAAGGATTTTAAAGG[A/C]GCCACCATAAAAAGT	100507650
rs531480431	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260441	ACATATGTTAGTCTA[C/T]GGGATTCCGTATGCA	100507650
rs531496431	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185092	TTTGTTGAGCTATCA[C/T]AGCAAAAGCTTTTTC	100507650
rs531562344	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184348	TTAAAATTAGCCGGG[A/T]GCAGTGGTGCAGGCC	100507650
rs531587713	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226904	GGGTTTGGCCTCTCA[C/G]ACTGCTAAGATTACA	100507650
rs531591293	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23234941	AATTAGGGCTGGGTA[C/T]GGTGGCTCATACCTG	100507650
rs531623730	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23272292	GGGCATGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	100507650
rs531651236	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23257075	GGAGAATCGCTTGAA[C/T]GTGGGTGGCGGAGGT	100507650
rs531746787	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23264958	TCCCGAGTAGCTAGG[A/G]TTACAGGCATGTGCC	100507650
rs531778064	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210615	ACCCCGTCTCTACTA[A/G]AAATGCAAAAAATTA	100507650
rs531785948	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221578	TTTTCAGCATTGGAC[A/G]GATCTCCCAGGTAGA	100507650
rs531816995	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23252856	TGAGAACAATGAGGA[C/T]GCAAATGGTCAGCAT	100507650
rs531831313	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265534	ATTCCCAAATCTCTT[C/T]TTTTAATTCTCCAAA	100507650
rs531840927	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23257884	GGTCACCAAGGCTGT[A/G]TAATAGCTATGAATG	100507650
rs531897498	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23245724	GACTCTCATATTTCA[A/G]ATAGTAGCCCCAACA	100507650
rs531909162	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23230515	AAAAATTAGCCGGGT[A/G]TGGTGGCGGGGGCCT	100507650
rs531929355	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250819	AACATTGGTTCGATC[G/T]GGAAAGGTGGGACAG	100507650
rs531947283	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23248302	TGGCTAGTTTTTGTG[-/T]TTTTTTTTTTTTTAA	100507650
rs531950726	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237850	GCCCCGCCCACGCCC[C/T]GCGCACGCCACGGAG	100507650
rs531952347	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258286	GAGGTTACGGTGAGC[C/T]GAGATCGCACTATTG	100507650
rs532084678	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23238445	ACACATCCTACGAAA[A/G]GTCCCGGTGCAGTGA	100507650
rs532162095	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183718	GCTCCGCCCCTGCCT[C/T]CTCTGCTCCCCTCCA	100507650
rs532168954	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23226001	AATGAAAAATTTTTT[A/T]AAAAATTAAAAAACT	100507650
rs532175336	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251703	CGCCTGTAATCCCAG[C/G]TACTCTGGAGGCTGA	100507650
rs532251130	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232704	TGGGGGGTCAGCCCC[C/T]GCCCGGCCAGCCGCC	100507650
rs532251624	in-del	-/T	0.370772	0.218893	intron-variant	RNF212B	GRCh38.p7	14:23248441	CCAACCCCAAGCCTC[-/T]TTTTTTTTTTTTTTT	100507650
rs532279252	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205252	ACCTTGTTTTATACA[C/G]AGCCTTTAAATGAGC	100507650
rs532300284	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23191382	AAGCAAGAAAGTCCA[C/T]CTCCATCCCATCACC	100507650
rs532320368	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23235516	AAAAATAAACAAAAC[C/T]GCCTTGCCACTTCAA	100507650
rs532320757	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213267	GCAGTGAGCCGAGAT[C/G]GCACCACTGCACTCC	100507650
rs532358272	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23189507	CTGTAATAACTCCCA[C/T]TGAAAAACAAACAGG	100507650
rs532363705	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190775	CCCCTGTTCAAAACC[C/T]TCCAACGCTGCCTGT	100507650
rs532405856	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222218	AGTTCTTTTGAAAAG[A/G]TGAACAAAATTGATA	100507650
rs532427177	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220563	GGGCTCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	100507650
rs532427699	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184282	ATCACGTGAGCCCAG[C/G]AGTCTGAGACCAGCC	100507650
rs532466493	in-del	-/C	0.177503	0.239258	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213692	GAACTGTGTGCTCTA[-/C]CTAAACAGGGTGACT	100507650
rs532470162	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221736	ATAGACGATATGTTA[A/G]GTCACCAAACAAATC	100507650
rs532525706	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23253223	CATAATATTATCAAA[G/T]TATCAGTCCCCATTC	100507650
rs532551933	in-del	-/A	0.327445	0.237702	intron-variant	RNF212B	GRCh38.p7	14:23233404	CAAGAATGATCAATT[-/A]AAAAAAAAAAAAAAG	100507650
rs532561120	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23220991	ATGGCAGGAGTAAGC[C/T]GCTATTTATCAATAA	100507650
rs532582163	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232056	TTGCAGCCTCTGCCC[A/G]GCTGCCACCCCGTCT	100507650
rs532596187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226681	CCGGTGGGTGATGGT[A/G]AGAGATGGCACAAGG	100507650
rs532596674	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236991	TTGTTTGAGGCAGTG[C/T]CTTGCTCCCTCAACC	100507650
rs532647066	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23264254	GTAATGTTCACCTTA[C/T]CTTTCCAGATTGAAG	100507650
rs532668745	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210602	CCAACATAGTGAAAC[C/T]CCGTCTCTACTAAAA	100507650
rs532677116	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251402	CTTCAGACTGGCCAA[C/T]AACAAACTTGAGGAT	100507650
rs532688887	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23272786	CCCTTTTTGCTGTTA[C/T]AAACACCCACATCTA	100507650
rs532738513	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215342	TTCTTTATAGCAGCA[A/T]CAAGACAGACTAATA	100507650
rs532739754	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221745	ATGTTAGGTCACCAA[A/G]CAAATCTGAAAACTT	100507650
rs532764753	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214109	TAGTGAGACTCTGTA[C/T]CTTTTTTAAAAAAGC	100507650
rs532831963	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229319	TGTTTCTATCTTTTG[C/G]TTATTGTGAATAATG	100507650
rs532886059	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269407	TAAGCAAAAAAGAAA[C/G]CTGGATAGCACTGTG	100507650
rs532899626	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193800	GAGTGGGGGTAGTTA[C/T]TAGAAGTTTTGTAGT	100507650
rs532951441	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213127	ACCATCCTGGCTAAC[A/T]CAGTGAAACCCCGTC	100507650
rs532964170	in-del	-/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23234260	TAGGATTTAAGTTGA[-/T]TTTTTTTTGTAATTT	100507650
rs533001975	snp	A/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23234336	CAAAAAGTTTTTTTT[A/T]AAATTACTTAGTCAA	100507650
rs533049083	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185076	ATTCCTTAAAATGAG[G/T]TTTGTTGAGCTATCA	100507650
rs533064071	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223368	AAGCCTTTCCTTTTT[G/T]TTTTTGAGATGGAGT	100507650
rs533092032	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23268638	TTGTCTTTACCCATT[C/G]TTTCTGGTGATTTCC	100507650
rs533127771	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260324	TCCTAAGAATGTTCT[A/G]TGTATTTATATAATT	100507650
rs533143318	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252693	TGAAGTCATGAGAAG[C/T]GGGGATGAAGAAATT	100507650
rs533227125	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208924	CCACTACGCCTGGCT[A/G]ATTTTTTGTATTTTT	100507650
rs533239450	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248553	TTCAAGCAATTATCC[C/T]GCCTCCACCTCCTGA	100507650
rs533244079	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206711	TAAGGTAGAGAGAGA[A/C]AAAATGTGGTGGTGC	100507650
rs533422818	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192886	CACCTGAGGTCGGGA[G/T]TTTGAGACCAGCCTG	100507650
rs533432670	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200336	CTCTCCCCCAACTTT[C/T]TTTTTTTGAGACAGA	100507650
rs533439669	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212368	GCTCTACTGCTTAAG[A/G]AGTAAAACTTAAAAG	100507650
rs533449853	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253247	CCCATTCACATTTCT[C/G]CAGTTGTCTCAGTTT	100507650
rs533452522	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206573	TTCTTTTTTCCTTTC[A/T]TAGACTGTCAAGATT	100507650
rs533522420	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23239912	GCGTGAGCCACTGTG[C/T]TTGGCCAGGATTGTA	100507650
rs533526857	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221858	AACTATATATATACA[C/T]GGAAATTGAACAATA	100507650
rs533541094	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23271311	AGCCAGGTGTGGTGG[C/T]GGGTGCCTGTAATCT	100507650
rs533562453	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23222650	GGCCAGTATTTCCCC[-/T]ATACCAAAACCAGAC	100507650
rs533666701	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222340	TTCAAAGGGTTATTA[A/G]TGGCTACTATGAACA	100507650
rs533672962	snp	C/G	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23233541	GACCAGCCTGGGCAA[C/G]ATGGTGAAACCCCAT	100507650
rs533714824	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23253473	ATGTTCCTCTGTCCT[C/T]TATTTCTTGTAAATT	100507650
rs533765201	snp	C/T			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274723	CCATCCTGGCTAACA[C/T]GATGAAACCCGTCTC	100507650
rs533792525	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23266027	TGTTGCCCAGACTGG[A/G]GTGCAGTGGTGCCAT	100507650
rs533817164	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23239339	TGCTGGGATTACAGG[C/T]GTGAGACACCATGCT	100507650
rs533840350	snp	C/G	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23217228	GGCAGAACCACCATA[C/G]ACCAGTGGTGGCAGT	100507650
rs533875440	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212606	TTTGAGACAGAGTCT[C/T]GCTCTGTCGCCCAGG	100507650
rs533995904	in-del	-/C	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23253271	CAGTTTTAAAATGTT[-/C]CCCACATTTTGAATT	100507650
rs533996321	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252890	GTGTGATGTGACTTT[C/T]GCAGCTAAAAGGAAG	100507650
rs533998272	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204906	TCTCTCAGCAGTGTT[A/T]TGTACTTTTCCTTGT	100507650
rs534051356	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207748	CCAAGGTTGAGAACA[C/T]GCCCCTCCATGACAC	100507650
rs534051414	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199330	GTCACAGATAGGTGA[A/T]ACACAAATGGTTACA	100507650
rs534056834	in-del	-/TG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197793	TCTTTTTTTTTTTTT[-/TG]AGCAACATGGCTGTT	100507650
rs534115842	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206981	CATGAAGGCCTTTCA[A/G]ATACAAACATGCACA	100507650
rs534121548	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210409	AGTAGGAAAATGAGA[A/T]TTGAACAAAGTCTGG	100507650
rs534131974	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205481	TTTTATTTTAATTCT[A/T]TACCTAGATTATTTA	100507650
rs534150544	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244173	TGGACATATAATGTA[C/T]ATCTAGAAGAGTGGA	100507650
rs534162419	snp	C/T	0	0	utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23237971	AAGCCAGCTGTTTAC[C/T]TTCCCGCCATGTCCA	100507650
rs534180214	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23268653	CTTTCTGGTGATTTC[C/T]ATCTTAGAGGGGAAA	100507650
rs534190652	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250843	GGGACAGCTCAAAGT[A/G]GGAAGGGGCTTCTAG	100507650
rs534194096	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23216017	TTGGGAGGCCAAGGC[A/G]GGCGGATCACGAGAT	100507650
rs534204851	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23257980	AAAAAAATCTCTCTT[C/T]TTGCACGGGATGAAA	100507650
rs534267656	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190491	TTTTTCTCATATATC[C/T]TACATTTGGTTTGTC	100507650
rs534330195	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254716	ATAAACAAACAAGAA[C/T]GTTTTGTTTACAATA	100507650
rs534341765	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23219936	CACCTGTAATCCCAG[C/G]ATTTTGGGAAGCCGA	100507650
rs534374658	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23238635	CCCAGCTACTCCAGA[A/G]GCTGAGGTGGGAAGA	100507650
rs534387764	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201672	TTTAATTTTGGAAAG[A/T]TTGTCAAATATAAAA	100507650
rs534425805	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23224865	TCCATCTGACAAGGG[A/G]TTAATAACTAGACTA	100507650
rs534450347	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23269280	TGCCCTCCAGCCTGG[A/G]TGACAGAGTGAGACT	100507650
rs534451579	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23246931	GGATCACCTGAGGTC[C/T]GGGGTTCGAGACCAG	100507650
rs534455652	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274630	GAACTGAAAATAGCC[A/G]GGCACGGTGGCTCAT	100507650
rs534456725	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208953	TTAGTAGAGACGGGG[A/T]TTCATCGTGTTAGCC	100507650
rs534487485	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236053	CAAATGTTCTTCACA[C/G]ACTCCAACCAAAACA	100507650
rs534517598	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202543	TACAGGGCCTAAAGA[G/T]GAGGCTTTAATTGCT	100507650
rs534546447	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273902	ATAGATGCTGAACTA[C/T]TTCCTTTTTACAGTT	100507650
rs534570640	snp	A/G	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23248589	TGGGATTACGGGCAT[A/G]CGCCACCACACCTGG	100507650
rs534610402	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208820	CTGGAGTGCAATGGC[A/G]CGATCTCAGGTCACT	100507650
rs534620055	snp	C/T	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23231811	CGCCTGACTGGTTTT[C/T]GTATTTTTTTGGTGG	100507650
rs534816936	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234562	TCCCAATTCTATGTA[C/T]ATAAAAATTCAATTC	100507650
rs534834912	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23190926	TCTGCCTCAGGGCCT[A/G]GTAGTAGCTGAAGCC	100507650
rs534858042	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242279	GGAGTGGTTTGTCTC[C/T]GTGAAGCATATGCCA	100507650
rs534920386	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23258981	CTTGAGGCCAGGAGA[A/G]GATCAGCCTGGGCAA	100507650
rs534953143	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23229995	CTTCTCCAATGTCTC[C/T]TTTTAAAGTTGTACC	100507650
rs534986840	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23233871	GGAAGCCAAGGTGGG[C/T]GGATCACCTGAGGTC	100507650
rs535003343	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261956	CTGGGTGACAGAGTG[G/T]GACTCTGTCTCAAAA	100507650
rs535061447	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212712	TTTTTTAATTTAATA[A/G]AGATGGAGTCTTGCT	100507650
rs535096298	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185642	CCTCTCAAATTATGA[A/G]CTAAGAAGCTAAGGG	100507650
rs535105569	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23261156	AGAACTTATGAAAAG[A/G]GGCAAAGGTAGAGGA	100507650
rs535111236	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200900	CTTATTGCACTTATG[C/T]AACTAACTGTATTGC	100507650
rs535162431	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193048	TGTGAGACGAGATCA[C/T]GCCATTGCACTCCAG	100507650
rs535191356	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207951	GCTTCCAGGTCACAG[A/G]TAAATGAGACATTGC	100507650
rs535212939	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223456	CGCCTCACGGGTTCA[C/T]GCCATTCTTCTGCCT	100507650
rs535215660	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221452	AGTGTAACAATTGTA[A/G]GTATATATGCACCCA	100507650
rs535247780	snp	G/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23241616	TTTAGTAGAGATGGG[G/T]TTTCACCATGTTGGC	100507650
rs535323146	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254130	AAGAAGAAAAAAATT[A/T]AAAAATTAGAGGGGT	100507650
rs535354327	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194586	CTACTAAAATAAAAA[A/T]TATCTGGGCGTGGTA	100507650
rs535360917	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261351	TGATTTCTTTATTAC[A/G]GCTAGCAGATATTTA	100507650
rs535412211	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201316	AGGCAACAATTGTCT[A/G]TGGATGACAAAAAGT	100507650
rs535473213	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198624	GAGGTTGCAGTGAGC[C/T]GAGATCGCGCCATGG	100507650
rs535516181	in-del	-/C	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23263115	TTTCCCTAAGCCAAA[-/C]TGTATCCAGCTTTAT	100507650
rs535518021	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23238745	TGTCTCAAAATAATA[A/G]TAATAATAATAATAA	100507650
rs535521191	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248308	AGTTTTTGTGTTTTT[C/T]TTTTTTTAATAGATA	100507650
rs535527790	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192128	TGGAAGACAGTGTGG[C/T]GATTCCTCAAGGATC	100507650
rs535632339	snp	A/T	0.000242365	0.0110056	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240381	CCAGTGCTTCCGAAA[A/T]GATGGGGCCCATTTC	100507650
rs535679797	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240946	TATTAGTAGAATCAT[C/T]TTACAAATGAAGAGA	100507650
rs535717509	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186508	GCACCTGCCACCATG[C/T]CTGGCTAATTTTTGT	100507650
rs535728071	snp	A/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260978	GTCATTTTTACTTCC[A/T]GCAGAAAGGGTACAC	100507650
rs535771197	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194110	GCCTCCCAAAGTGCT[A/G]GGTTTACAGGCATGA	100507650
rs535791738	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23239311	GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGC	100507650
rs535793291	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185543	TATGATGCAGACTTA[A/T]TGTGGGATAAAACAT	100507650
rs535876933	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23193027	AACCTGGGAGGTGGA[A/G]GTTGCTGTGAGACGA	100507650
rs535882067	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246702	CAAAGTGCCAGGATT[A/G]CAGGTGTGAGCCACC	100507650
rs535966208	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23233142	AAACATGTGCTGTGT[C/G]CACTCGGGGTTAAAT	100507650
rs536056746	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272989	AAATGTATCCCTGCA[C/T]TGTTTCCTAGTTTCA	100507650
rs536061484	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23218095	AATTGCAGGCCAGGC[A/G]CTGTGGCTCATGCCT	100507650
rs536104662	snp	C/T	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23228928	TTCAGTGGCATTAGG[C/T]ACATTCACAATGTTG	100507650
rs536114659	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215597	AGTGCTGAAAGAAAG[C/G]AACTGTCCATCCAGA	100507650
rs536177437	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23267637	TTTCACCATGTTGGC[C/T]AGGCTGGTCTCGAAC	100507650
rs536275250	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251749	TGAACCTGGGAGGTG[A/G]AGGTTGCAGTGAGCC	100507650
rs536279405	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236164	AATGTAAAAACGATG[A/C]CACTCTTCTCACTAA	100507650
rs536308883	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23219694	TCAGGCTGGTCTCAA[A/T]CTGCCGACCTCAGGT	100507650
rs536312028	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208925	ACTACGCCTGGCTAA[-/T]TTTTTTGTATTTTTA	100507650
rs536341534	snp	A/C	0.000798403	0.0199641	missense, synonymous-codon, nc-transcript-variant	RNF212B	GRCh38.p7	14:23262933	TCTCTTTCAGTTACC[A/C]CACGACCCAGTTTCC	100507650
rs536364350	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232104	TCTGCCTGGCTGCCC[A/G]TCGTCTGGGATGTGA	100507650
rs536370828	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23258183	GTCTCTACTAAAAAT[A/G]CAAAATTAGCTGGGC	100507650
rs536371709	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23238123	CATCGCCTCTGGAAA[A/G]CAGGGGAATTTTGCC	100507650
rs536437490	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23226369	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	100507650
rs536444442	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214323	ACATAGTGAAACCCC[A/G]TCTCTACTAAAAATA	100507650
rs536463464	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263789	GTGCTAACAACATAT[A/G]AAGCTAGGTTTTCTG	100507650
rs536498638	snp	A/G	0.0123036	0.0774623	intron-variant	RNF212B	GRCh38.p7	14:23232227	GGCTGCCCATCGTCT[A/G]AGATGTGGGGAGCGC	100507650
rs536590794	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23189079	ATACAGAGCACAGAT[C/T]TCAAGCAGGCCCTTA	100507650
rs536592216	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23216360	AGTAACCTACAAAAA[A/G]GCAAAAAGAAGTGAA	100507650
rs536614045	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23186565	CTGTTGGTTAGGCTC[A/G]TCTTGAACTCCTAAC	100507650
rs536616729	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23242333	CATTTGTCTTAATCA[A/G]TGACCAGTCCCACTA	100507650
rs536630601	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209028	CTCCCAGAGTGCTGG[A/G]ATTACAGGCGTGAGC	100507650
rs536706746	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219568	CCTCTGCCACCTGGG[C/T]TCAAGTGATTCTTGT	100507650
rs536709401	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23258769	ATTGCTCCATATGTA[C/T]TTGTTTGTTTGGGAA	100507650
rs536772211	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202692	CTGTCTCTACTAAAA[A/G]TACAAAAAATTAGCC	100507650
rs536774790	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219419	AAAGAGAAAGAACAA[A/G]AAGTTTAAAAGCAGA	100507650
rs536850192	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196253	ATCCTCTGAGTGCCC[A/C]CTGTCTCTCTGTCAT	100507650
rs536947612	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225620	AAAACAATTCATGAA[A/G]ATAGAGAATAGAAGG	100507650
rs536998366	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189143	TAACTGACCTTTCCA[A/G]TTACCTGCTCCTCTC	100507650
rs537017775	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190706	CCCCTACACTTTATT[C/T]TCTACACGGCAGCCA	100507650
rs537027113	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23238728	GAGACAGAGCCAGAC[C/T]CTGTCTCAAAATAAT	100507650
rs537075195	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234650	GATTCTGTTTCATTG[G/T]TCTACACGTTTATGC	100507650
rs537109422	snp	C/G	0.000363306	0.013473	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269887	TGCCTCCTCTGGACA[C/G]GGGATTTTTTCTTTC	100507650
rs537118330	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23261846	GGAGGACACCTGTAG[-/T]CCCAGCTGCTCGGGA	100507650
rs537132597	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236088	ACTGCAAAAGTTAAT[G/T]CAGAAGCAAATATAG	100507650
rs537153849	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230814	GTGTAAGGTAAGGAT[C/T]CAACTTTATTCTTTT	100507650
rs537207550	snp	C/G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200067	CAACGAGTGTACTAT[C/G/T]GTCTTGAAACATTTT	100507650
rs537207761	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232068	CCCGGCTGCCACCCC[A/G]TCTGGGATGTGAGGA	100507650
rs537268259	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271267	AATATGGTAAAACCC[C/T]GTCTCTCTCTACTGA	100507650
rs537269966	snp	A/C	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23261980	CTCAAAACAAACAAA[A/C]AAACAGAAAACAAAA	100507650
rs537270780	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236581	ACAAACAAACACACA[C/T]TTAATGGGGTTTATT	100507650
rs537271016	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231873	TCTCCAGCTCCTAAC[C/T]GTGAGTGATCTGCCA	100507650
rs537289665	snp	A/G	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23223657	ACCGCGCCCGGCCAA[A/G]CCTTTCTTTTCAGAT	100507650
rs537346055	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255695	TATAGCAAGATATCA[G/T]TTCTAAAAAAATTTT	100507650
rs537383507	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23194587	TACTAAAATAAAAAT[C/T]ATCTGGGCGTGGTAG	100507650
rs537457611	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23189391	CTTCCCTATCCTATC[G/T]CCCAAAGTCTCAAGA	100507650
rs537472969	snp	C/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23232445	GGAGCGCCTCCGCCC[C/G]GCAGCCGCCCCGTCT	100507650
rs537598140	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23269033	CAGCAGGCTGGGTGC[A/G]GTGGCTCACGCCTGT	100507650
rs537612718	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252110	GGGCGTGGGAAGAAA[A/G]GTTGGGACCCCAACC	100507650
rs537627677	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23231829	ATTTTTTTGGTGGAG[-/A]GGGGGTTTCGCTGTG	100507650
rs537652284	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258721	TTTTTTTCTAAGAAG[A/T]GACAGTCCTTATTGT	100507650
rs537664480	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23229841	AAGAAACAGAAAAAC[G/T]ATATTCCCAATAAAA	100507650
rs537686181	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218874	AGATTTAACCCAAAG[A/G]AGAGTACCTCCGGGC	100507650
rs537692224	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214256	CCCAGCATTTTGGGA[G/T]GCCAAGGCAGGTGGA	100507650
rs537700685	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208961	GACGGGGTTTCATCG[C/T]GTTAGCCGGGATGGT	100507650
rs537749623	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23248595	TACGGGCATGCGCCA[C/T]CACACCTGGCTAATT	100507650
rs537831603	in-del	-/AA	0.302435	0.244439	intron-variant	RNF212B	GRCh38.p7	14:23226297	GCAAGAAACCGTCTC[-/AA]AAAAAAAAAAAAAAA	100507650
rs537926993	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183833	TTTCTTTTTGCAATC[G/T]TCTCTCGCTTTCTCC	100507650
rs537935741	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265982	GGTTGTTTGTTCATT[C/T]GTGTTTTTTTTTGAG	100507650
rs537976574	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274522	GTTTTTTACAAGCTC[A/G]GTGGGGGAAGATTTT	100507650
rs538016739	snp	C/T	0.0146672	0.084371	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195281	GAAAAAAAAAAAACC[C/T]ATGAGATGCAGCTAA	100507650
rs538018598	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23216831	GTTGCAGTGAGCTGA[G/T]ATTGCCCTACTGCAT	100507650
rs538042107	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23252137	AACCCTCTAAACAGT[A/G]TTTGGTTCCCCTGGC	100507650
rs538068406	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244113	AAACAACAGATGGAA[A/G]CATTATTTGTGACCA	100507650
rs538079965	snp	A/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215733	AATGGCTAATGAAAA[A/T]TTTTCAAACAGAAAG	100507650
rs538107641	snp	C/T	0.0154538	0.0865337	intron-variant	RNF212B	GRCh38.p7	14:23248201	GGTGCAATCATGGCT[C/T]CCTGCAGCCTTGCCC	100507650
rs538138063	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232270	GCCCCATCTGGGATG[C/T]GAGGAGCGCCTCTGC	100507650
rs538156258	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211271	TTAGATAAAAATGGA[C/T]GAACTCCTTGAAAGA	100507650
rs538169304	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23264907	GCTCACCACATCCTC[C/T]GCCTCCCATGTTCAA	100507650
rs538184400	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197015	CTTTTTTTGCTCACT[A/G]ATGTCTTCAGGGCCC	100507650
rs538202543	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23250168	TTTATACCTGAAATG[C/T]CTGATTTCTACACTT	100507650
rs538219795	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23248971	CTGCTGTTGTAGCAT[A/G]GAAGCAGCCATAGAC	100507650
rs538225356	snp	A/G	0.00676609	0.0577691	intron-variant	RNF212B	GRCh38.p7	14:23232255	CGCCTCTGCCCCGCC[A/G]CCCCATCTGGGATGT	100507650
rs538244570	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23256799	TCAAGCAATCCACCC[A/C]CTTCAGCCTTTCAGG	100507650
rs538263370	in-del	-/ACT	0.00676609	0.0577691	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237100	CCCTAAGTAGCTGGG[-/ACT]ACTACGGGCACCCGC	100507650
rs538277620	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237311	ATTTTTGTATTTTTA[G/T]TAGAAGCGGGGTTTC	100507650
rs538290709	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23269271	TGGTGTCACTGCCCT[C/G]CAGCCTGGGTGACAG	100507650
rs538376966	in-del	-/A	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23192688	TTAAAGTATAATAAT[-/A]AAAAAAAAGAATATT	100507650
rs538377341	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23257166	ACACACACACAAAAA[A/C]AATAAAATAAAATAA	100507650
rs538392003	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23273077	CAGTGGTCAGGTCTT[A/C]CAAAAGGCTAGTGCT	100507650
rs538394617	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189668	AAAAAAATTAGCTGG[A/G]TGTGGTGGTGCATGC	100507650
rs538403024	snp	C/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183744	CTCCATCCTCAGTCC[C/G]GTCTCCTCCCTCCTC	100507650
rs538431651	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23188461	GACAAAGATTAGGGT[-/T]TTTTTTTTTTTTTTT	100507650
rs538442234	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23216201	CAGTGAGTCAAGATC[A/G]TGCCACTGCACTCCA	100507650
rs538450148	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23257964	TTGAAAAACAGTTTT[A/T]AAAAAAATCTCTCTT	100507650
rs538471677	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265148	AAATAATGATATTTT[C/T]GTCTTCCAACTAATA	100507650
rs538509602	snp	A/G	0.00636936	0.0560724	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210762	AGTCCAGGTGACAGT[A/G]TGAGACTCTGTCTCA	100507650
rs538511283	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189697	GCCTGTAGCACCAGC[A/C]ACTCAGGAGGCTGAC	100507650
rs538554714	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251600	GCGGGCAGATCACCT[A/G]AGGTCAGGAGTTCGA	100507650
rs538592920	snp	C/G/T	0	0	intron-variant	RNF212B	GRCh38.p7	14:23258047	ATATTCTCATTAAGA[C/G/T]AGTAAAAGGGGCCGG	100507650
rs538631763	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219742	CTCCCAAAGTGCTGG[A/G]ATTACAGACATGAGC	100507650
rs538649135	snp	C/T	0.00358779	0.0422022	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196918	TTTCAGAGTCCTCAC[C/T]TGTGATAACTAGAGT	100507650
rs538704564	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190312	ATCTAACCACCTAAT[C/T]GATGTCTCTGTTTTG	100507650
rs538712175	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23261114	CAGACCTCACATTCT[A/G]TATTTGTTCCGATTG	100507650
rs538768567	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220088	ACTCCAGAGGCTGAG[A/G]CACGAGTATCCCTTG	100507650
rs538815283	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221245	TAGGAAAAAAAAAAA[A/G]AAAGAAAGAAACACG	100507650
rs538877931	snp	A/T	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23220704	GTGGCGGGCACCTGT[A/T]GTCCCAGCTACTCAG	100507650
rs538879112	snp	C/G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194659	AGAATCGCATGAGCC[C/G/T]GGGAGATGGAGGTTG	100507650
rs539023640	snp	C/T	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23217268	GGTGGGGGGGGGGCT[C/T]CTCTGCCTGTGGAAA	100507650
rs539041258	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23222925	CGGGCATGGTGGCAC[A/G]CACCTGTAATCCTAG	100507650
rs539053996	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263135	TCCAGCTTTATTAAA[C/G]ATACTGTCCATTCAG	100507650
rs539061233	snp	A/G	0.00835141	0.0640778	intron-variant	RNF212B	GRCh38.p7	14:23242512	TTCTTACAGTGCCCA[A/G]TGTGTGCCTGCTGTC	100507650
rs539128687	snp	C/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215225	TGTAAGGTGTGCCTT[C/G]CTTCTCCTTCATTTT	100507650
rs539155632	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23255906	TTTGATATAGGCTAA[A/G]CATTTGTACCCTGGC	100507650
rs539162853	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218079	AAATTCTAGAGTTGA[A/G]AATTGCAGGCCAGGC	100507650
rs539168307	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263740	TTCTATTAGTGACAT[A/G]TGCCCCTTCCCCCAA	100507650
rs539173681	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212160	GCACTTAGGAGAAAA[C/T]TGTAGCCAGCCTTAT	100507650
rs539192412	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250599	AGTTCATGTGTCAGA[A/G]TGTCTCTTCTACTAG	100507650
rs539219748	snp	C/T	0.00716266	0.059414	intron-variant	RNF212B	GRCh38.p7	14:23240192	CTGTATATGTACATA[C/T]ACTTCTTTACAACCA	100507650
rs539243795	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23186210	TAGGTTGGAATCTTT[C/T]TGTGACATAAACTCT	100507650
rs539246898	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23272450	AACAAACAAACAAAC[A/G]ACCGAAAATGTGAAA	100507650
rs539282779	snp	C/T			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270256	TGAAAATGCTGGGCG[C/T]TCAGTTCTGAGGATT	100507650
rs539311102	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203777	GCCACCATGGTAGGC[C/T]TTACTTTAGTTATTT	100507650
rs539444050	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23262164	TAAACACTGTTCTGA[-/T]TTTTTTTTTTCATCT	100507650
rs539447881	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23262373	TGGACAGATGTATGG[C/T]TGAGAGTACTTGGTA	100507650
rs539461883	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222419	AGACATATACAACCT[A/G]CCAAGATTGAACTAT	100507650
rs539464960	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259649	GGAAATGGAATTCTT[A/T]GCAAATTCCCCTGAA	100507650
rs539520152	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253518	GGGTTTATCACCATC[A/T]TTGGTTTGGGGGCGG	100507650
rs539613913	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23228102	AGGCGTGGTGGCACA[C/T]GCCTGTAATCCCAGC	100507650
rs539629168	snp	C/G	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274643	CCGGGCACGGTGGCT[C/G]ATGCCTATAATCCCA	100507650
rs539646922	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191030	CAAATATCACCTGCT[C/G]AAGGGGGACTTCTCT	100507650
rs539656695	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199150	TTGGGGACATGTGTC[C/T]GTGACAGCCTCAGGA	100507650
rs539706995	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23240653	AAATGATTTAGCAAA[C/T]CTATTACTTGAGGAC	100507650
rs539745394	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200073	GTGTACTATCGTCTT[A/G]AAACATTTTTTTCTC	100507650
rs539791941	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23245921	CTCAAGACGTTGTCA[C/T]TGAATGAATGAATGA	100507650
rs539819267	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211181	TGAGATTGCACCACT[A/G]CCCTCCAGCCTGGGC	100507650
rs539829032	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251999	GGAGTTGTTATGAAC[A/G]TTCCATTACATAGGC	100507650
rs539833832	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23245759	TACTCCTTACCATGC[-/T]TTTTTTTTGCATTGT	100507650
rs539862019	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23251220	TTTTCTGATACCAAC[C/T]AGTTCTCTGACACCA	100507650
rs539897095	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215846	TATCCTTCTCCTAGT[C/T]CTTATCCATTCTTAG	100507650
rs539993821	in-del	-/C	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23261980	TCAAAACAAACAAAA[-/C]AAACAGAAAACAAAA	100507650
rs540005681	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23233003	ACAGAGAAATCAGAT[A/T]GTTGCTGTGTCTGTG	100507650
rs540008552	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23232675	CAGGCCAGCCGCCCC[A/G]TCTGGGAGGGAGGTG	100507650
rs540080837	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242663	CCACAGAAGAAAATT[A/G]GGAATTTATAAAAAG	100507650
rs540084080	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23239248	TATTTTTAGTAGAGA[C/T]GGAGTTTTGCCACGT	100507650
rs540086607	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23264808	CATGTATCCATACAT[A/G]TATTACAAGGTTTTT	100507650
rs540091096	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23248082	CATCCTCACATGGCA[A/C]AAGTGGCAAACAGGC	100507650
rs540096361	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266760	GTGGTCTATCCTGGA[A/G]AATGCTCCATGTGTA	100507650
rs540101105	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184642	ATCCTGCAACTTCTA[A/G]TATTTTTGCATTTAT	100507650
rs540132414	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23228835	GGGCTTGAATATGTA[C/T]AGAACACTGATTTTC	100507650
rs540289256	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23224373	AGAGCTAAAGTAACC[A/C]AAACAGCATGCTACT	100507650
rs540291032	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205124	ACATTTACTATAAAA[G/T]ATTCTTTCTCATATA	100507650
rs540324972	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23239318	ACCCACCTCGGCCTC[C/G]CAAAGTGCTGGGATT	100507650
rs540335452	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189443	CTTCTCTCCTACATC[A/G]TCAGTTTTTCACTGT	100507650
rs540364733	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232172	GGAGGGCCTCTTCCC[C/T]GCCGCCATCCCGTCT	100507650
rs540385175	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205948	GTATGAAATTTGCTT[A/G]ATTAATAATGCAAAC	100507650
rs540404660	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196623	TTTTAAAATATTTTT[A/T]TAGAGATGGGGTCTT	100507650
rs540424575	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198073	TTTACTTCTTTTGTG[C/G]ATCTTCAGTTACTTC	100507650
rs540455415	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23251892	AGTATGTGAGGAGGG[C/G/T]TGCAGAGCTTCCATA	100507650
rs540458734	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226027	AAACTCGGCTGGGCG[C/T]GGTGGCTCACGCCTG	100507650
rs540516182	snp	C/T	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23232850	GTGCCTCTGCCCAGC[C/T]GCCCCGTCTGGGAAG	100507650
rs540529093	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23257604	AGGAAGCAGATGAGA[C/T]GTAAATACTGCTGTG	100507650
rs540532218	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220922	ACTAAAAGGAAGAGA[A/G]GAAGGAAGGAAAAAA	100507650
rs540566529	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198710	CTGTATGTAAACACT[A/T]TACTCTAGCTGGTAA	100507650
rs540601021	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23221848	GAATTTTGGAAAGTA[C/T]ATGAACACATGGAAA	100507650
rs540616292	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23264795	CTGACAGTGATTCCA[C/T]GTATCCATACATATA	100507650
rs540637467	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23243557	AAAAATTAGCCAGGC[A/G]TGGTGGTGCGGGCCT	100507650
rs540687837	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23262873	ACAAATTGGCCAGGC[A/T]AGGCAGGCATACCAT	100507650
rs540760809	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200658	TGAGGATCCAAGATA[A/C]ATCTGGGGCTTCCGT	100507650
rs540762291	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234835	AATCCCAGCTGCTGG[A/G]GAGGCTGAGGCAGCA	100507650
rs540795246	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223589	CTCGATCTCCTGACC[C/T]CGTGATCTGCCCGCC	100507650
rs540814469	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273225	TGGGGATTGTGATGG[A/G]TCATATACTCATCAC	100507650
rs540825190	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189830	GTGAAAAAATGAACA[A/G]AACTTCCCTTGATGC	100507650
rs540849283	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209178	ATGGCATTTGTAAAC[A/T]GTCATGGTGCTGGTG	100507650
rs540853605	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232288	GGAGCGCCTCTGCCC[A/G]GCCGCAACCCCATCT	100507650
rs540870708	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186609	CGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACT	100507650
rs540880120	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265311	AAAGAAGGTTCACAG[A/G]ATGCTGATTGTTGGC	100507650
rs540930336	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23218993	ACCAATATGTCTGGC[A/G]GCAGACTTTTCAGTG	100507650
rs540930496	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223808	TCAAATTATCCTTGT[C/T]TGCAGTTGTCATAAT	100507650
rs540962095	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203385	GCTATAAACATGTGC[A/G]TGCAAATATCTTTTT	100507650
rs540976456	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234324	TGTGTGTACATGCAA[A/C]AAGTTTTTTTTAAAA	100507650
rs541014111	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23266364	CCAAATTTCCTACTG[C/T]TATTGATTTTGACTT	100507650
rs541080408	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23218813	CTTCCTAAACCTAGA[A/G]AAAGATATCAACATT	100507650
rs541098227	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23268543	TTTATGGAGGAGGAA[A/G]TTTTTGGAGGTCTTT	100507650
rs541208400	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184913	AGTTATTTTTAGCCT[A/T]ATTAAATATATTATG	100507650
rs541208915	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269339	AACTCTGCCAGCAGT[A/C]CTGGGATTACTTCTC	100507650
rs541210469	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259266	CTGATAACACTCATT[A/G]TAGCCTCAATCTCCT	100507650
rs541219136	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23261337	AACATAAAGTACATT[A/G]ATTTCTTTATTACGG	100507650
rs541294668	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23257710	ATAGACACATTAGTA[C/T]AGCAAATGGTAAAGT	100507650
rs541295183	in-del	-/CTA	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23234652	TTCTGTTTCATTGGT[-/CTA]CACGTTTATGCACCA	100507650
rs541381442	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270168	AGCACTCATCCTGTC[A/T]CCAGTCGAGTCCTAC	100507650
rs541392982	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253660	ATCCTTAATTCATTA[C/G]AAGTTGTAAAATTCC	100507650
rs541406149	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229001	ACAGAAACTCTTCAC[C/T]CATTAAGCAATTACT	100507650
rs541408132	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23222109	CAAACCAAACCCAAA[A/G]TTAGGAGAAAAAAAG	100507650
rs541420623	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207201	CTGAGTGTTCTAAGT[G/T]TAAGTAGGAATTAAC	100507650
rs541472637	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260158	ACACTTGTAACCCAT[C/T]CCTGAACATCAGTGA	100507650
rs541515816	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200205	TATTTTTTACATAGG[C/T]TTTTAAATGGGCTTT	100507650
rs541520850	snp	G/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23233495	CTTTAGGAGGCTGAG[G/T]TGGGAGGATCAGTTG	100507650
rs541538270	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240209	CTTCTTTACAACCAA[C/T]TGGAATACCCACAAT	100507650
rs541545155	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222583	TACCAATCCTATTCA[A/G]ACTGTTCTGAAAAGT	100507650
rs541566002	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23221784	CTGAAATAATATCAG[C/G]CATCTTCTCTGACCA	100507650
rs541607382	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237002	AGTGTCTTGCTCCCT[C/T]AACCAGGTTGGAGTG	100507650
rs541620773	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218192	GCTAACACGGTGAAA[C/T]CCCGTCTCTACTAAA	100507650
rs541631011	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253208	CTAAAATAACAATTC[C/T]ATAATATTATCAAAT	100507650
rs541657765	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234063	GATAGTACCACTGCA[C/T]TTGCACTCCAGCCAT	100507650
rs541709733	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269217	GTTGAGGCAGGAGAA[C/T]TGCTGAATCCAGGAG	100507650
rs541739898	snp	C/G	0	0	intron-variant	RNF212B	GRCh38.p7	14:23247867	TGTTTTCCCAAGTGG[C/G]TGTACCATTTTACAT	100507650
rs541741757	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23239856	ACTTTTGACTTCAGG[G/T]GATCCACCTGCCTCG	100507650
rs541780474	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247070	ACTTGAACCTGGGAG[A/G]TGGAGACTGCGGTGA	100507650
rs541785125	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23267435	TGTCTCTTGTAACAA[-/T]TTTTTTTTTTTTTGG	100507650
rs541812174	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23234985	TTGGGAGGCCGAGGC[A/T]GGTGGATCACGAGGT	100507650
rs541812884	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247010	CCAGGTGTGGTGGCA[C/T]GTGCCTTTAATCCCA	100507650
rs541816386	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190711	ACACTTTATTCTCTA[C/T]ACGGCAGCCAGAATG	100507650
rs541836082	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274160	TTGCCATATAGCTGA[G/T]CCCAACTGATGAAAA	100507650
rs541848930	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23257893	GGCTGTGTAATAGCT[A/G]TGAATGTGGAGGCTG	100507650
rs541878091	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192801	AATTTTTTAAAAATA[C/T]AGCTTTATGGCCAGG	100507650
rs541941268	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199666	AAGATTTTTAGCAGG[A/T]TGTGAAGTCTCATGT	100507650
rs541953283	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191224	CCAGGGCTGGTGGCG[A/G]TGCACACCTGTAGTC	100507650
rs541969277	in-del	-/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23243148	TTCAGTTAAGAACCC[-/T]TTTTTTCTTCCTTTG	100507650
rs541999901	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265572	CCTCTAAATCTCCCA[A/C]ATTTGAAATCTCCCA	100507650
rs542034305	snp	A/G			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23195126	AGAAGTTAACTGACA[A/G]TGAAAGTACTGCATA	100507650
rs542040219	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185113	AAGCTTTTTCAAATG[A/G]GGTAAAGTCCAATCA	100507650
rs542071480	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218985	AATAGAGCACCAATA[C/T]GTCTGGCAGCAGACT	100507650
rs542075756	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206249	CCAGCTAATTTTTGT[A/G]TTTTTAGTAGATACA	100507650
rs542138747	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211551	AATCATACAAAGATC[A/G]TACCAGAAAACTAAA	100507650
rs542149484	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246511	CACATGTAATATGAA[A/T]TAATAATACTTATCC	100507650
rs542176197	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202068	CCAGCTTGACCAACA[C/T]GGTGAAACCCTATCT	100507650
rs542177257	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23185967	TAGCTGGGTGTGGTG[A/G]CTCACGCCTGTAATC	100507650
rs542180187	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23217431	AGTCCTGGGGAACTC[A/G]CTGCCCTGAAGAGAA	100507650
rs542219393	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232812	AGCCTCTGCCCGGCC[A/G]CCACCCTGTCTGGGA	100507650
rs542219446	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23227655	CACCCAGGCTGGAGG[C/T]AGTGGTGCAATCACT	100507650
rs542221942	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187830	CCCAGAGTCCCAGGG[A/T]TCACTGCCTATGGTC	100507650
rs542239514	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215103	GATTGGATCATGCGG[A/G]CAGTTTCCCCCATAC	100507650
rs542259532	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266247	TATACCCATGCTGAT[C/G]CCATTCCAAAGTATT	100507650
rs542278763	snp	G/T	0.0174175	0.0916809	intron-variant	RNF212B	GRCh38.p7	14:23232628	CCGGCCAGCCTCCCC[G/T]TCCGGGAGGGAGTTG	100507650
rs542361138	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23271379	ACCCAGGAGGCGGAG[A/C]TTGCAGTGAGCCGAG	100507650
rs542363442	snp	A/G			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199390	AGGAGGCAATCAGAT[A/G]TGCATCTATCTCAGT	100507650
rs542439752	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214491	AGAGTGAGACTCAGT[A/C]CCCCCAATAATTAAA	100507650
rs542471300	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209704	TTTCAAAGAATAGAT[A/G]GAAAGGGAAAAATAG	100507650
rs542471573	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203065	TGATTTGTGAGATTT[G/T]GGTGTACCCATCACC	100507650
rs542474350	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23256105	TGGGGTCTGTTTATG[C/T]ACTTACGACCCTTGG	100507650
rs542501092	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219911	ACAAGGGCCTGGGCA[C/T]GGTGGCTCACACCTG	100507650
rs542570556	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23252515	AGTACACCAAGACAC[G/T]GGGTTGCAGCAGAGA	100507650
rs542600345	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23218976	AAATAACAAAATAGA[A/G]CACCAATATGTCTGG	100507650
rs542614574	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23224110	ACACACAAAGGAAAG[A/T]TATTTCATGTTCACG	100507650
rs542614687	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231891	GAGTGATCTGCCAGC[C/T]TCGGCCTCCCGAGGT	100507650
rs542625773	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213768	AGGTAGAGAGAGAGA[A/G]AGAGAGGCAGAGAGA	100507650
rs542629115	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253908	TTCTAAAACTTAGTG[A/G]CTTATTTACAGATGT	100507650
rs542642459	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218905	ATTTAATAATCAAAC[C/T]CCCAAAGGTCAAGGA	100507650
rs542661991	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223545	TATTTTTAGTAGAGA[C/T]GGGGTTACACGATGT	100507650
rs542673133	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261601	TCAGGTACCATGTTA[C/T]AGGCTGGATATATAC	100507650
rs542682099	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23252746	CCTCTGTGGGGGTCT[G/T]TAGACTCACTGTTCC	100507650
rs542705143	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23248462	TTTTTTTTTTTTTGA[A/G]ACAGAGTCTTGCTCT	100507650
rs542935577	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250206	TAAGTTAGGCCAGCC[A/G]TGGTGGCTCACGCCT	100507650
rs542936673	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256852	TTATCACGCCTGGCT[A/G]AATTTTTTAAATTAT	100507650
rs542937213	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243026	GGGAGATGGGTAGAC[A/G]TACGGTGTGAAAGCC	100507650
rs543025562	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213048	CCGGGCATGGTGGGT[C/T]ATGCCTGTAATCCCA	100507650
rs543035004	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23191539	GGGTAATGATATTAC[A/C]GTTATTGTTAAAAAG	100507650
rs543045772	snp	C/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184331	CCCGTCTACTAAAAA[C/T]TTTAAAATTAGCCGG	100507650
rs543087189	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187676	GAGGTTACCAACAAA[C/G]GACCCAAATCTCTCC	100507650
rs543092748	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197464	CCCGGGAGGCGGAGG[C/T]TGCAGTGAGCTGAGA	100507650
rs543094207	in-del	-/AACA	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23272426	CCATCTCAAAAAAAC[-/AACA]AACAAACAAACAAAC	100507650
rs543100898	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208880	TCTCCTGACTCAGCC[A/C]CCTGAGTAGTTGGGA	100507650
rs543104782	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270255	TTGAAAATGCTGGGC[A/G]CTCAGTTCTGAGGAT	100507650
rs543139948	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194974	TGAAATCATACAGCA[A/T]CACACAGATTCTTGG	100507650
rs543147950	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186792	AATTAGAAACCTGAG[A/G]CTTAAAGAAATATTT	100507650
rs543164908	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235072	CAAAAATTAACCAGG[C/T]GTGGTGGCAAATGCC	100507650
rs543216911	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23219511	CAGTCTCACTCTGTC[A/G]CGCAGACTGGAGTGC	100507650
rs543239111	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208966	GGTTTCATCGTGTTA[A/G]CCGGGATGGTCTCGA	100507650
rs543270675	snp	C/T			utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274131	TAGATGGTTAACTCA[C/T]TGATGATACCTATTT	100507650
rs543280249	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23224061	TGAAGAAAACTATAA[A/G]ACATTGATGAAAGAA	100507650
rs543373519	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201887	CAAATTTTGTAAGCA[A/G]TCTATAAAGTTTATT	100507650
rs543393913	snp	G/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23235609	CCTTTGGAAAACTTG[G/T]ACCTGCAACTGACAG	100507650
rs543426075	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260371	TCCTGTAATTATTCT[A/G]GCACATTGTAGTGTG	100507650
rs543464230	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23185692	TTCTTGGAATACAGC[A/G]GTACTAGGTGCACAC	100507650
rs543476317	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221345	AGAGCAAGAATAGCT[A/G]TAGTTATAAAAGACA	100507650
rs543503225	snp	G/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215503	GAGCAAGACTCTGTA[G/T]CTTTAAACAAACAAA	100507650
rs543532141	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23231184	TAGGGATGACATTGA[A/G]TCCGTATATAGCTTT	100507650
rs543537880	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260853	AGTAAAATCTTAATT[C/G]TAATGCTCACCCTGG	100507650
rs543547106	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269412	AAAAAAGAAAGCTGG[A/C]TAGCACTGTGTTTAA	100507650
rs543594569	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23187307	TGATAGTTAAAACAC[-/A]AAACACACACAACCC	100507650
rs543655812	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23262320	TATTTTTCTAGTTTC[C/T]TAAGGTGGATGAGAG	100507650
rs543691754	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248772	AAGGACACTAATCCC[A/G]TTCACAAGAGCAAAG	100507650
rs543709209	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200936	GTTAAGAAGCTCACA[A/T]ATAGTTTTCAAATTC	100507650
rs543748252	in-del	-/A	0.00874735	0.0655527	intron-variant	RNF212B	GRCh38.p7	14:23232811	AGCCTCTGCCCGGCC[-/A]GCCACCCTGTCTGGG	100507650
rs543759580	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241348	TGAAGTAGGCAGTGT[C/T]GGATGATGGAAGGCT	100507650
rs543764850	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255377	TAGGAATCCAGAGCA[C/T]GAAGACCATGATATC	100507650
rs543766726	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263234	CAAAAATCAGAAAGC[C/T]ACTATAAAACCCAAT	100507650
rs543807124	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23217619	AAGGGAAAAGAATAA[A/G]AGTCTCTGCTTGGTA	100507650
rs543824523	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222717	CTCTGATGAATATTG[A/G]TGCGAAAATGCTAGT	100507650
rs543851859	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23250076	ACACAAGTTATTACG[C/T]AAGGTTATTTATTAC	100507650
rs543892764	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251041	GCTTAGTGATTTGGG[A/G]GGTCCAACATATTTT	100507650
rs543918751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220518	GCCTGGGCAACATAG[C/T]GAGACTCTGTCTCAA	100507650
rs543929645	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23257464	AAAGGAAACTCTTAA[A/G]TACAATTCTTTAGTA	100507650
rs543985419	in-del	-/AA/AAA	0.193966	0.243639	intron-variant	RNF212B	GRCh38.p7	14:23240034	ATAACCTCACCACTC[-/AA/AAA]AAAAAAAAAAAAATC	100507650
rs543995361	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23240621	CATTAATAAAGAATG[G/T]TCCTAAATTATTTAG	100507650
rs543995887	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23248021	TAACAGATTCAGTGT[C/T]GGGGGAGGGCTTACT	100507650
rs544007129	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213239	AATGGCGTGAACCCG[G/T]GAGGCGGAGCTTGCA	100507650
rs544057099	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204093	TTTTCTTACTGATTT[C/G]TTTGAGTTCGTTGTA	100507650
rs544073295	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23186077	TGCACTCCAGCCTGG[G/T]TGGCAAAGTGAGACC	100507650
rs544079561	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244654	ATTAATTAATTTCTA[C/T]GACTAAAGGTTGTTT	100507650
rs544160719	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220742	AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGATG	100507650
rs544180837	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209168	TGACGTTGCCATGGC[A/T]TTTGTAAACTGTCAT	100507650
rs544197988	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197381	AAAATACAAAAATTA[G/T]CCATGTGTGGTGGTA	100507650
rs544207960	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23264733	AAGATCTGCGGATTT[C/T]TGGTTTTCTATGCAT	100507650
rs544244580	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242593	TGTACTCTTCCTCAC[G/T]CTTGTAAATGTACTC	100507650
rs544327579	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215740	AATGAAAATTTTTCA[A/G]ACAGAAAGGAAATGA	100507650
rs544383346	snp	A/C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209000	CCTGACCTCGTGATC[A/C/T]GCCCGCCTTGGCCTC	100507650
rs544398565	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210902	TCTAAAATTATTCCA[A/G]AATAAAAAGCTATTT	100507650
rs544440684	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23231922	GCCGGGATTGCAGAC[A/G]GAGTCTCGTTCACTC	100507650
rs544440797	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236767	AAAAAGTTTGAGAAC[A/T]ACTACTCTAAGTGGA	100507650
rs544448958	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23223337	GCTAATATTACACTG[A/C]ATGGAGAAAAACTGA	100507650
rs544535250	snp	C/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23263961	GGCATGGTGGTGCAC[C/G]CCTGTAGTCCTAGCT	100507650
rs544617092	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23272588	AATAGTTTAATTTTC[A/G]AATATTCATCCTTAT	100507650
rs544632524	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23223504	GGACTACAGGCGCCC[G/T]CCATCAAGCCCGGCT	100507650
rs544667362	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23244555	TACAAATTTCAATCA[C/G]TTAACTTTTTATTGA	100507650
rs544668611	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23243495	GAGCTCAGGAATTTG[A/G]GACCACCCTGGGCAA	100507650
rs544672341	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23230392	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	100507650
rs544734759	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210586	TTTGAGACCAGTCTT[A/G]CCAACATAGTGAAAC	100507650
rs544783459	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196550	GCTCAAGCAATCCTC[C/T]CGCCTCAGCCTCCTG	100507650
rs544797410	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23252391	TTAAAAAAAAGTTTA[C/T]TATGATTTCATCACA	100507650
rs544815758	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23188883	ATAAATATGATTGAT[C/T]GAATGAATTAATGTA	100507650
rs544853324	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209882	GACTGGCCCAGTGAG[G/T]TGACTCAAACCTGTA	100507650
rs544897632	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250288	GTTCAAGATCAGCCT[A/G]GCCAATATGGTAAAA	100507650
rs544911289	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23218738	GGAGGTAACCTTAAA[A/G]AGGAGGTAGAGAAAG	100507650
rs545019704	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232129	ATGTGAGGAGCCCCT[C/T]TGCCCGGCTGCCCAC	100507650
rs545046872	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219455	GAAGTTGAAGTGTAG[C/T]GCTCTCCTTCTTCTC	100507650
rs545049513	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23220553	CAAAACAGCCGGGCT[C/T]GGTGGCTCACGCCTG	100507650
rs545059517	snp	C/T	0.00358779	0.0422022	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213890	TAAATGGAAAAAACC[C/T]CAACAGTCAACAGGC	100507650
rs545092873	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255311	AGTTAATATCTTTAA[A/G]CTAAATTTGTTGTAA	100507650
rs545132726	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273538	CACTATCACTGAGAT[C/T]AAACATGTATTCTAC	100507650
rs545133264	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23225705	TAGTTAATGCATACC[-/A]AAAAAAAATAGAAAG	100507650
rs545152572	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236286	TTTGGGAGACCAAGG[C/T]AGGTGGATCATGATG	100507650
rs545194687	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208975	GTGTTAGCCGGGATG[C/G]TCTCGATCTCCTGAC	100507650
rs545213843	snp	C/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23235802	CAGTTTGGTCTAAAT[C/G]TATGATGTTACAAAA	100507650
rs545239888	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204006	GCATACGTTTGTTTG[C/T]CATTTGTATATCTTC	100507650
rs545267072	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271519	TTTTTTAATGGCTTG[A/G]GTTTTGAGCATATTT	100507650
rs545303213	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210497	AGAAATGTAGGATGG[A/G]GTGGGCGTGGTGGCT	100507650
rs545322160	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250881	GTAGATAAGAGACCA[A/G]TGGTTGCCTTCTTTT	100507650
rs545357965	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243651	CAGTGAGCTGAGCTC[A/G]CGCCACTGCACTCCA	100507650
rs545368724	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23231910	GCCTCCCGAGGTGCC[A/G]GGATTGCAGACGGAG	100507650
rs545444711	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209138	CCCCTTTTTAGACCA[C/T]ATAAGATAACTTCCT	100507650
rs545468949	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23238844	AAGTATATGAAATTG[A/G]TATTGGCAGAAAATA	100507650
rs545520427	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211052	GTGAAACCCCGTCTC[C/T]ACTGAAAATAAAAAA	100507650
rs545530828	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207009	ACACATACACACACA[C/T]ATCTTGGGTGTGTTA	100507650
rs545543261	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23272116	TCATTATACTATTCT[A/G]TGTATTTTTTGAAAA	100507650
rs545545658	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23233361	TATTGTCCTATGACC[A/C]TGCCAAATGCCCCTC	100507650
rs545577860	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23246946	CGGGGTTCGAGACCA[A/G]CCTGACCAACATGGA	100507650
rs545606811	snp	A/C	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23232874	TGGGAAGTGAGGAGC[A/C]CCTCTGCCCGGCCAC	100507650
rs545647678	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23267197	GTTCTGCCCTGGCTG[G/T]TCTCGAACTCCTGGG	100507650
rs545651883	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23219478	TCTTCTCCTTCTAGT[-/T]TTTTTTTTTTTTTGA	100507650
rs545652728	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206098	CTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC	100507650
rs545667557	in-del	-/AAAAAAAAA	0.214239	0.247429	intron-variant	RNF212B	GRCh38.p7	14:23193092	AGAAAAACTCTGTCT[-/AAAAAAAAA]AAAAAAAAAAAAAAA	100507650
rs545752559	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195663	GCTCTCCCGACAGCA[A/C]ATCCACCCTCCTAAT	100507650
rs545760706	snp	C/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184255	AGCGCTTTGGGAGGC[C/T]GACAGGGGAGGATCA	100507650
rs545788029	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255942	GCAAAATCACTGCTT[C/T]TTTAATACTCCTTGC	100507650
rs545808302	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23252342	ATTTCTTACACCACA[C/T]CCTGTTCAAAAGATC	100507650
rs545831113	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232318	TGGGAGGTGAGGAGC[C/G]TCTCTGCCCGGCTGC	100507650
rs545955482	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221483	ATGCTAGAGTACCCA[G/T]ATATATAAAGCAAAT	100507650
rs545973303	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23223624	CCTCCCAAAGTGCTG[C/G]GATTACAGGCGTGAG	100507650
rs546000765	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23228211	CACTCCAGCCTGGGT[A/G]ACGAGAGCGAAACTC	100507650
rs546012248	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23245318	TGGTTGAGCCATCAT[A/G]TTTGACATACACTAT	100507650
rs546019581	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191418	CTTGCCTTTTATAAT[A/G]TCTGCCATTACTTAA	100507650
rs546021490	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273301	ATTGCCAATGTTAAC[A/G]AGCAATATCTCTGTT	100507650
rs546088475	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216340	GCAATTCTAAACAAT[A/G]TTCAAGTAACCTACA	100507650
rs546152306	snp	A/G			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274693	TGGGCGGATCATGAG[A/G]TCAGGAGATCAAGAC	100507650
rs546155636	snp	G/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23192542	GGACTGTTGTGGGGT[G/T]GGGGGAGGGGGAAGG	100507650
rs546172222	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23238070	GGTAGGGAGTGTAGC[A/C]AGAAAAAGAACTGAG	100507650
rs546175803	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23239094	TTTCAGATGGAGTCT[C/T]ACTCTGTCGCCCAGG	100507650
rs546224097	snp	C/T			missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23260663	TTCACCTATAGGAAT[C/T]TCCAAGTCGGTACCA	100507650
rs546250667	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274056	TTGAGAGAGAAACAA[C/T]TTTATTTTTGGCCTT	100507650
rs546251604	in-del	-/C	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23241831	GCTCATGCCTGTAAT[-/C]CCAGCACTTTGGGAG	100507650
rs546253490	in-del	-/AAC			intron-variant	RNF212B	GRCh38.p7	14:23240137	TATATAAAATGTTAT[-/AAC]AACCTGCTGTTATAA	100507650
rs546269412	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232551	CTCTGGGAGGGAGGT[A/G]GGGGTCAGCCCCCGC	100507650
rs546280977	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211286	CGAACTCCTTGAAAG[A/G]CATAAACTACTAAAA	100507650
rs546292229	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23262014	AACTCTCTCTATATA[C/T]ACACACACACACATA	100507650
rs546320999	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244700	TTTTTCTCAGCAGAT[A/G]GATGCACCTTCTAAA	100507650
rs546356647	snp	A/C	0.0123036	0.0774623	intron-variant	RNF212B	GRCh38.p7	14:23232245	ATGTGGGGAGCGCCT[A/C]TGCCCCGCCGCCCCA	100507650
rs546379418	snp	A/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183391	TGAAGACAAAAGTAG[A/T]TTTCATTAACGGTAG	100507650
rs546384277	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273625	GCCTTAAGCAAAAAT[A/T]CTGGAAAAACAGAAA	100507650
rs546404904	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23265404	TTTGGGTCTGCTTAC[A/T]TAATTTCTTACCTAA	100507650
rs546408026	snp	A/G	0.00795532	0.062565	intron-variant	RNF212B	GRCh38.p7	14:23227563	GAATATACATTAAAT[A/G]TCAATATACATTGAA	100507650
rs546419925	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237276	CTGAGATTACAGGTG[A/C]GTGTCGCCACACTCG	100507650
rs546464006	snp	A/T	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23265643	GTCAGGTTGGTAACA[A/T]CAGTGTTCTCTTTTT	100507650
rs546547458	snp	G/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23232037	GCCTCCCAAAGTGCC[G/T]AGATTGCAGCCTCTG	100507650
rs546565393	snp	A/G	0.0138799	0.0821421	intron-variant	RNF212B	GRCh38.p7	14:23193240	AAATTATACATAGCC[A/G]AAGTATCAATCAAAA	100507650
rs546566412	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23266145	TGTATTTTTAGTAGC[A/G]ACGGGGTTTCACCAT	100507650
rs546567817	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23222343	AAAGGGTTATTAATG[A/G]CTACTATGAACAACT	100507650
rs546568193	snp	C/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199216	CAGCTTAGTTTTATA[C/T]ATTTTAGGGAGGCAT	100507650
rs546606857	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195857	GTTGTTTTGCATTTT[A/G]CAAAGGAGGAAACGG	100507650
rs546666576	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210018	ATTAGCTGGCATGAT[A/G]TGTGTGCCTGTAATC	100507650
rs546684804	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225418	CTTAAGTGTCCATCA[A/G]CAGATGAATGGATAA	100507650
rs546739859	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204536	CTCAGTTGGCTGTAA[G/T]TATTTGGTTTATTTC	100507650
rs546747026	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263715	TCCCATCAATCCAGC[C/T]TCGGAGACTTTCTAT	100507650
rs546761658	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220548	AAAAACAAAACAGCC[G/T]GGCTCGGTGGCTCAC	100507650
rs546791562	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232401	GTGAGGATCCCCTCC[A/G]CCCGGCAGCCGCCCT	100507650
rs546851080	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214750	CAGATTTAACATTTG[C/T]GTCATTGTAGTCCCA	100507650
rs546861488	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256531	TGCACGCCACCATGC[C/T]TGGCTAATTTTTGCA	100507650
rs546907645	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23221191	CAGGAGTTTGAGACG[A/G]GCCTGGCCAGCATGG	100507650
rs546912352	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220015	ATGGTGAAACTCCAT[C/T]TCTACCAAAAATACA	100507650
rs547066059	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23192866	GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGGTC	100507650
rs547083644	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222878	GCTAACATGGTGAAC[C/T]CCCGTTTCTACTAAA	100507650
rs547094403	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23233502	AGGCTGAGGTGGGAG[A/G]ATCAGTTGAGCCCAG	100507650
rs547096915	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23240207	TACTTCTTTACAACC[A/G]ATTGGAATACCCACA	100507650
rs547154139	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23264113	AAACAAAAAAACAAC[A/C]ACAATAAAAAGTAAA	100507650
rs547218519	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223335	CAGCTAATATTACAC[C/T]GAATGGAGAAAAACT	100507650
rs547218792	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23217907	GGCACCAGGGATCAA[C/T]ACTGGAGAAACAGGG	100507650
rs547249224	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248103	GCAAACAGGCTCCTT[C/T]AAGCCTCTTTTTATT	100507650
rs547260739	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23261085	TGCTGTGTCCGGTTT[C/T]CATTGGCTGGAACCA	100507650
rs547268066	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260050	TTTCTCATCATGGCA[C/T]ACACAGAAATTGATA	100507650
rs547315449	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23257139	GCCTGGGCGACAGAG[C/T]GAGACTCAGTCACAC	100507650
rs547327533	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209544	GATATAAACAAATGA[C/T]TGACTAAAAGACTAA	100507650
rs547336319	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247519	ATAATGTATGGTCTT[C/T]TGTGACTTGCTGCAT	100507650
rs547449465	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274750	TCTCTACTAAAAATA[C/T]AAAAAAGTAGCCGGG	100507650
rs547490874	snp	C/T	0.00159617	0.0282053	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274689	AAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATCA	100507650
rs547561780	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198500	CCAACATAGTGAAAC[C/T]CCCGTCTCTACTAAA	100507650
rs547571637	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206401	TTCAGTATCTGATTT[A/T]CATGCTTGTATTTTT	100507650
rs547624664	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205485	ATTTTAATTCTTTAC[C/G]TAGATTATTTACGAA	100507650
rs547681193	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258091	CGCCTGTAATCCCAA[C/G]ACTTTGGGAGGCTGA	100507650
rs547727119	snp	C/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214213	CAAAGAAAAACTAAG[C/G]CTGGGCATGGCGGCT	100507650
rs547742220	snp	A/G	0.170084	0.236883	intron-variant	RNF212B	GRCh38.p7	14:23232896	CCCGGCCACCACCCC[A/G]TCTGGGAGGTGTACC	100507650
rs547757014	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23258423	GGAAGTTGTGAATTA[A/G]GCCAGATGTTCTAGA	100507650
rs547797818	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229425	ATTGCTGGGTCACAT[A/G]GCAGGATAGTTCTAT	100507650
rs547804605	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23232725	GCCAGCCGCCCCGTC[C/T]GGGAGGGAGGTGGGG	100507650
rs547840173	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221721	GGGTAATTCTTAAGG[A/C]TAGACGATATGTTAG	100507650
rs547871474	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198923	GGTTAGCTAGCTTGG[C/T]ATATATATAGACAGA	100507650
rs547872101	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211133	TGAGGCAGGAGAATT[A/G]CTTGAATCTGGGAGG	100507650
rs547872468	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23245904	TTAATAAGTAGTGGA[C/T]GCTCAAGACGTTGTC	100507650
rs547912069	in-del	-/A	0.00517822	0.0506191	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185291	GACAAGGCAGGGAAT[-/A]ATATAGCACGAAACT	100507650
rs547925050	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23258230	GTAAACCCAGCTATT[C/T]GGGAGGCTGAGGCAG	100507650
rs548007922	snp	G/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23190406	CCTGATTTTTGCCCA[G/T]TATTCCCCACTTTAG	100507650
rs548014084	snp	C/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23238674	GCCCAGGAGTTCCAG[C/G]CTGCAGCGAGCCCTG	100507650
rs548023682	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23232634	AGCCTCCCCGTCCGG[C/G]AGGGAGTTGGGGGGT	100507650
rs548030743	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246602	ACTTTAAAAAAAAAC[A/C]AACAAAAAACAGAGA	100507650
rs548036096	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253439	GATTTTGTTTATTGT[A/G]CCTATGGAGTCATTT	100507650
rs548049440	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23232936	ATTGAGAACGGGCCA[A/T]GATGACGATGGTGGT	100507650
rs548161222	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190886	CAGTCTCATAGGCCT[C/T]CTTCCTAGTCCTTGA	100507650
rs548205381	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274561	CAAACAATGAACAGA[C/G]TGAGGATTTTGGAAA	100507650
rs548225201	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254057	GCCGAAGTGGGAGAA[C/T]GGCTAGATCCCAGGA	100507650
rs548239223	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23256723	TTGGGCTGTTGCTCT[A/G]TTGCCCAGACTGCAG	100507650
rs548241195	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23231431	AAACACACCCACATA[C/T]GCACATGCAAACTTT	100507650
rs548274565	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184439	GCTGCAGTGAGCTAT[A/G]ATGACGCCACTGCAC	100507650
rs548277497	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23253775	TATAGTTCAAAAATA[C/T]TAAGACTTGCTTGTA	100507650
rs548293684	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23261621	TGGATATATACCACC[A/G]GTCCTTTCTAATTAG	100507650
rs548336150	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183839	TTTGCAATCGTCTCT[C/T]GCTTTCTCCATCTTT	100507650
rs548349517	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259487	TGCTTCAAGCATTTA[C/T]ATGTTAACTTTCTTT	100507650
rs548395223	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23220858	AAAAACAAATACACA[A/G]AAAATAAAAGCAGGA	100507650
rs548396108	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222272	AAAAAAAAAGAAGAC[C/T]CAAAGAAATAAAATC	100507650
rs548416015	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236331	GCAGCCTGGCCAACA[C/T]GGTGAAACCCCGTCT	100507650
rs548417550	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210639	AAAATTAGCTGGGTG[A/T]GGTGGTGTGAGCCTG	100507650
rs548472838	snp	C/T	0.00874735	0.0655527	intron-variant	RNF212B	GRCh38.p7	14:23257986	ATCTCTCTTCTTGCA[C/T]GGGATGAAAAATTAT	100507650
rs548477049	snp	G/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260463	CCGTATGCACTCTTA[G/T]GAAGAACTAAACTTT	100507650
rs548640040	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226932	ACAGACATGAGCCAT[C/T]ACACCCGGCCCTTCA	100507650
rs548658430	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258302	GAGATCGCACTATTG[C/G]ACTCTAGCCTGGGCA	100507650
rs548720170	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185346	AAATGAAAAAATGTC[A/G]AATTTGCCTCTAGCC	100507650
rs548741320	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23257894	GCTGTGTAATAGCTA[C/T]GAATGTGGAGGCTGA	100507650
rs548774345	in-del	-/CTCTTTTAGGCAAGGGCCTGTCCTGTAGCAAATG	0.00636936	0.0560724	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273758	ATTTCTAGATACCTT[lengthTooLong]GAGTTACCTCCAAGA	100507650
rs548781364	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23192873	AAGGTGGGCGGATCA[A/C]CTGAGGTCGGGAGTT	100507650
rs548815712	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23251874	CAAATGGAAAAGATG[A/C]AAAGTATGTGAGGAG	100507650
rs548816407	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213579	GCTAAACTTCCACCC[C/T]GACTCGGCAGCAAGA	100507650
rs548820287	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198410	TGGAGCCAAGCGTGG[C/T]GGCTCACGCCTGAAA	100507650
rs548888575	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202409	CCAAATCGGCCCTTA[C/T]AATCTTTGATCTTAT	100507650
rs548938712	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23187978	ATAGGTCAGAAAGAA[A/C]GGAAGATGAAATGAG	100507650
rs548983127	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247271	GTAATTTACATACCA[A/T]AAAATTTACCCTTTT	100507650
rs548995940	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218489	GAGTTTGAAGACAAG[A/C]TATTTGAAAATACAG	100507650
rs549031552	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23223640	GATTACAGGCGTGAG[C/T]CACCGCGCCCGGCCA	100507650
rs549039458	snp	C/T	0.0217236	0.101931	intron-variant	RNF212B	GRCh38.p7	14:23242222	CCTTTTAAAGTTCGC[C/T]AATGTAAAAAGCTGT	100507650
rs549056118	snp	A/G	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23248584	GTAGCTGGGATTACG[A/G]GCATGCGCCACCACA	100507650
rs549058162	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255454	GAAGTAGATAGTTTC[A/T]TACCAATAAAATGTT	100507650
rs549146189	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254649	TCTGCCCACCTTGGC[C/T]TCCCAAAGTGCCAAG	100507650
rs549167716	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200435	GGATCAAGCAATTCT[C/T]ATGCCTCAGCTTCCC	100507650
rs549180325	snp	G/T	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23241626	ATGGGGTTTCACCAT[G/T]TTGGCCAGGCTGATC	100507650
rs549210799	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214185	GAAAGTCTCAGCAAA[A/G]AAATAGAAGATACAA	100507650
rs549295803	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186203	CTCTCTGTAGGTTGG[A/C]ATCTTTTTGTGACAT	100507650
rs549363046	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186136	AACAAACAAACAAAG[C/G]TAGGAAAGGAATCTC	100507650
rs549463553	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223376	CCTTTTTTTTTTTGA[G/T]ATGGAGTCTTGCTCT	100507650
rs549530501	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213486	TCCACCAGGAGTCAT[C/G]AGGCGGAAAGAAGAA	100507650
rs549532168	in-del	-/TGCAGCCT	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23248204	GCAATCATGGCTCCC[-/TGCAGCCT]TGCCCTCTTGAGCTC	100507650
rs549547377	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23229865	AATAAAACATGCCCA[A/G]CTGTCCAGATAGTGG	100507650
rs549578927	snp	A/C/T			intron-variant	RNF212B	GRCh38.p7	14:23227099	TTATTGGTTTTGATA[A/C/T]TGTATTATATTTATA	100507650
rs549586769	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229008	CTCTTCACCCATTAA[A/G]CAATTACTTCCTATC	100507650
rs549591928	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219082	TTTTACCTTAGAATA[C/T]ATTCAGTGAAATATC	100507650
rs549632034	snp	G/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214847	CCAAATCTGTTGAAA[G/T]AAATAAGGCCACAAA	100507650
rs549662618	snp	C/G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23268736	CAGACTCATGAAAGG[C/G/T]AGAGGAAAGCACCTA	100507650
rs549669295	in-del	-/CT	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236506	GGCGACAGAGTGAGA[-/CT]CTGCTTCAAAAAACA	100507650
rs549690707	in-del	-/C	0.00636936	0.0560724	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197974	GTACATTCTTAAGGG[-/C]GGGGGAGATTACAAA	100507650
rs549694958	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223425	CAGTGATATGATCTC[A/G]GCTCACTGCAACCTC	100507650
rs549811345	snp	G/T	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208929	ACGCCTGGCTAATTT[G/T]TTGTATTTTTAGTAG	100507650
rs549835734	snp	A/C	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23248559	CAATTATCCTGCCTC[A/C]ACCTCCTGAGTAGCT	100507650
rs549853123	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261744	AGGTGGGCGGATCAT[A/G]GGGTCAGGAGATTGA	100507650
rs549853376	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254044	AACACTTTGGGAGGC[C/T]GAAGTGGGAGAACGG	100507650
rs549940968	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23261147	TAGCAACTTAGAACT[C/T]ATGAAAAGGGGCAAA	100507650
rs549954600	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274644	CGGGCACGGTGGCTC[A/G]TGCCTATAATCCCAG	100507650
rs549963143	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23248304	GGCTAGTTTTTGTGT[G/T]TTTTTTTTTTTAATA	100507650
rs550014336	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254551	CCAAAGCATATATTA[C/G]TTTTTTGTATGTGTG	100507650
rs550014851	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193622	CTAAGAAGAACTAGC[A/G]ATAGTGACACAGAAA	100507650
rs550019083	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185301	GGGAATATATAGCAC[A/G]AAACTCCATGGGAGG	100507650
rs550164475	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252716	AAGAAATTGCATTCT[C/T]ATGCTGATTCAGTTC	100507650
rs550210942	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240058	AAAAATCTCACCACT[C/G]TCTGTCCATTACTTT	100507650
rs550228465	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23217119	GGACCAGAGTGGAGC[C/T]CCCTGCCCTGAAGGG	100507650
rs550231293	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23188091	GTCTTCTAGGGTTTA[C/T]GCAGTCCTGAGAATT	100507650
rs550252300	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206846	AGCAAAACAAACAAA[C/T]AAACAAAAAATCAGG	100507650
rs550274745	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23246687	CCCACCTTGCCCTAC[A/C]AAAGTGCCAGGATTA	100507650
rs550390565	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199239	GGAGGCATGAGACAT[A/C]AATCAATATATGTAA	100507650
rs550397742	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240039	CCTCACCACTCAAAA[A/G]AAAAAAAATCTCACC	100507650
rs550412905	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23267586	GGCATGTGCCACCAC[A/G]CCTAGCTAATTTTTG	100507650
rs550417685	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190009	GTTGGACCACCGGTG[C/G]TCCAATCTAGCAATC	100507650
rs550432553	snp	C/T	0.000223439	0.0105674	intron-variant	RNF212B	GRCh38.p7	14:23243249	TTTTTTTCCCTTTTC[C/T]TCCCAGAAAAATGTG	100507650
rs550434354	snp	C/G	0.00716266	0.059414	intron-variant	RNF212B	GRCh38.p7	14:23230531	TGGTGGCGGGGGCCT[C/G]TAGTCCCAGCTACTC	100507650
rs550434356	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212838	AAGACAATACCACTT[C/T]TTAGTTTTTGTTTAT	100507650
rs550449418	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229345	TAATGCTGGTAGGAA[C/T]ATTGGTGTACACATA	100507650
rs550522019	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230861	TTCCCAGCACTGTTT[A/G]TTGCAGAGACTGTTC	100507650
rs550522119	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235879	AATTTTAATGTAACC[A/G]GCTATAAAAAGTTCA	100507650
rs550567637	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23264435	ATAGTGAAAGTGTTT[A/G]AGGACTCAATCAACA	100507650
rs550578513	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209529	ACATGCCTCCATACT[A/G]ATATAAACAAATGAT	100507650
rs550600202	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23226310	TCAAAAAAAAAAAAA[A/G]AAAAAATTAAATAAA	100507650
rs550604288	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272921	CTGATCTATACATGC[C/T]GCTGAAGGATGGACT	100507650
rs550641556	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243855	GCTGATGCGGGTGGA[C/T]CACCTGAGGTCAGGA	100507650
rs550642360	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214694	AATAATAATCAAAAT[A/G]GAGAGAAAACGGGCA	100507650
rs550661053	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231734	CGGCTCACTGCAACC[C/T]CCCTGCCTGATTCTC	100507650
rs550742379	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201252	TCAAGAGCACCTGTT[A/G]TAGTTTAATAGCTGG	100507650
rs550756069	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232211	AGGAGCGTCTCTGCC[A/C]GGCTGCCCATCGTCT	100507650
rs550760939	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271006	TGGGTAGGGGTACTA[C/T]TTGAACTAGGAAAAA	100507650
rs550794568	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203605	TGCCTCAGCCTCTCA[A/G]GTAGCTGAGATTATA	100507650
rs550904684	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255765	TCTTCTTTGGAAAAA[C/T]GAAAGAGACCAACCT	100507650
rs550954573	snp	C/T	0.0209421	0.100162	intron-variant	RNF212B	GRCh38.p7	14:23242219	TGACCTTTTAAAGTT[C/T]GCTAATGTAAAAAGC	100507650
rs550957711	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211631	CATAAAAAGGATAAT[A/G]CGTCATGAACAAATT	100507650
rs551027839	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206275	ATACAGGGTTTCACC[A/G]CGTTGGCCAGGCTGG	100507650
rs551033369	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208192	TTTTAGAGCTGGGTC[A/G]AGGAAAGCACGAGAT	100507650
rs551075597	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23255510	CAATATTTAACACTT[A/G]CATTATCCAGACAAT	100507650
rs551115371	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23187262	GACACCTACTGGACA[A/G]AAAAGGTTATGGCTT	100507650
rs551126284	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225185	GATGTGGAGAAGAGA[A/G]AGCCCTTGTACACTG	100507650
rs551139394	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203197	TATGCCTGTGTATCT[A/T]TATAGCTTAGCTTCC	100507650
rs551188286	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209009	GTGATCCGCCCGCCT[C/T]GGCCTCCCAGAGTGC	100507650
rs551203185	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202589	GGGCGTGATGGCTCA[C/T]GCCTGTAATCCCAGC	100507650
rs551213397	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196679	ACTCCTGGTCTCAAG[C/T]AATCCTCCTGCCTAG	100507650
rs551222000	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185100	GCTATCATAGCAAAA[A/G]CTTTTTCAAATGGGG	100507650
rs551236959	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23248970	TCTGCTGTTGTAGCA[C/T]GGAAGCAGCCATAGA	100507650
rs551276917	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196015	TTTTCTGTCTCAGTT[A/G]CTTTCAATCATGACA	100507650
rs551304197	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214295	GGTCAGGAGTCTGAG[A/G]CCAGCCTGGCCAACA	100507650
rs551347395	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189081	ACAGAGCACAGATCT[C/T]AAGCAGGCCCTTAAC	100507650
rs551382650	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213637	TCCTGGAAAGGTGTC[A/G]GTGGGACCCAGTGGG	100507650
rs551383503	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240680	GGACTAGAATGTACT[C/T]GTTAGTGTTTTGAAG	100507650
rs551419327	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249713	GAGGTAGTATTCCTT[C/T]GATCATACAAACTGT	100507650
rs551501424	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256279	TTGGCTGTCTATTAT[A/G]TAGCTTTATCTCTGT	100507650
rs551525144	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208464	ATCACACTGCACTCT[A/C]GAATGGGTGACAGAG	100507650
rs551590216	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209334	GACCTATCTCATCCT[C/G]TGACTTAGAATGCCT	100507650
rs551626437	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243082	TGGAAACACTTGTTT[A/G]GAGAACAGAGCTTAA	100507650
rs551631037	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23262759	GAGATGAATATCCTT[C/T]CCTTATGTAGAAGAT	100507650
rs551667294	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23270816	TTCCAGAATGGTCTC[A/G]ATTTCAGATTTTATC	100507650
rs551668737	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23272121	ATACTATTCTATGTA[G/T]TTTTTGAAAATGTGG	100507650
rs551682514	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187050	CCCCAACATTTGTCA[A/C]CCCCTTCGCACAGTC	100507650
rs551688771	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23186029	CGTGTGAGCCATGGA[G/T]GTTGAGGCTGCAATG	100507650
rs551729532	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208907	GGGACTACAGGTGCC[C/T]GCCACTACGCCTGGC	100507650
rs551738887	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236552	AAAAAGCAAAAAAAC[C/T]CCAAACAACAACAAC	100507650
rs551815397	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23186347	ATTAAATTTTGAGCA[C/T]TTTTTTTTTTTTTGA	100507650
rs551831571	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232705	GGGGGGTCAGCCCCC[C/G]CCCGGCCAGCCGCCC	100507650
rs551864743	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205283	TTGGAATTAGACAAA[A/G]ATTTTTCTCTTTTTT	100507650
rs551876976	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23228783	GGCATCAAGACAGAC[A/T]AATCAATCAGTGGAA	100507650
rs551889777	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234595	CATGCACACTTACCA[A/G]TTAAAATTTATTAAC	100507650
rs551892003	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23238501	GGGAGGCCAAGGAAG[A/G]AGGATCGTTTGAGTC	100507650
rs551905895	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23231460	TTAATCCATACCTCA[A/C]ACCATGTAGAAAATT	100507650
rs551919061	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193916	GCGCGATCTTGGCTC[A/G]CTGCAACCTCCGCCT	100507650
rs551929060	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23265750	CTGTATTACTTCTTC[C/T]ATTATCTGTTTCATT	100507650
rs551995904	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23246828	TGAAGATCATATAAG[C/T]GAAAAGAAGTTTGTA	100507650
rs552075909	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187852	CCTATGGTCGATTAG[A/G]TGGGGCCTTCCTGAG	100507650
rs552091012	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23219283	GTACCCAGAAAACCA[C/T]AGAATAGTATAACAC	100507650
rs552095976	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23266487	TGCAATCTCGGCTCA[C/T]CGCAACCTCCGCCTC	100507650
rs552151444	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23189518	CCCATTGAAAAACAA[A/G]CAGGCCGGACTGGGT	100507650
rs552163680	snp	C/T	0.0051642	0.0505513	intron-variant	RNF212B	GRCh38.p7	14:23262724	CAGGTGGAGAACATT[C/T]TTCCCCTAAATATCT	100507650
rs552194828	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23261881	GAGGCAGGAGAATGG[A/C]GGGAACCCAGGAGGC	100507650
rs552241390	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220564	GGCTCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	100507650
rs552302057	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225548	TGTTAAGTGAAAAAA[C/G]CCAGGCACAGAAAGA	100507650
rs552323510	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23190317	ACCACCTAATTGATG[C/T]CTCTGTTTTGGGTGT	100507650
rs552346710	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183770	TCCTCTGCAATTTAA[A/G]TATTAGCACAAAGCC	100507650
rs552362246	snp	C/T			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207322	CAGGCTGTAGACTGC[C/T]CTCTACTATTCTAGA	100507650
rs552380032	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23220992	TGGCAGGAGTAAGCT[G/T]CTATTTATCAATAAT	100507650
rs552384249	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215387	GAAACAAAGATTCAA[A/G]TGACAGTGTATTTCT	100507650
rs552432567	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23222257	GCCAGACTGAATAAG[-/A]AAAAAAAAGAAGACC	100507650
rs552434383	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200084	TCTTGAAACATTTTT[C/T]TCTCTCTCTCTCTAG	100507650
rs552452603	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23240020	CACACACACACACTC[A/C]TAACCTCACCACTCA	100507650
rs552473227	snp	A/G	0.00358779	0.0422022	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213747	GAGAGAAGAAGTGAG[A/G]AAGAGAGGTAGAGAG	100507650
rs552492003	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216598	TAATAAGGCCAATCT[A/G]GCTGGGTGTGGTGGC	100507650
rs552495558	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23226126	AAGATGGTGAAACCC[C/T]GTCTGTACTAAAAAT	100507650
rs552509248	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23250648	AAACCCGGAAAATCT[A/G]AGACAAGTCTCAGTT	100507650
rs552524172	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23272812	ATCTACCTTCTTGTC[C/G]TCTGCTGCAGACTCT	100507650
rs552557380	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23232176	GGCCTCTTCCCCGCC[A/G]CCATCCCGTCTAAGA	100507650
rs552581647	snp	A/C	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23263749	TGACATGTGCCCCTT[A/C]CCCCAAAAAAAACGA	100507650
rs552610656	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23235342	GCAGCAGAGGGAGAC[A/G]CCCATCTCTTAAAAA	100507650
rs552648675	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23258024	AAGGGTCATTCTACT[A/G]TGGTAGAATATTCTC	100507650
rs552698619	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231894	TGATCTGCCAGCCTC[A/G]GCCTCCCGAGGTGCC	100507650
rs552698631	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201623	TGTAATATCTTAAAG[A/G]AGTAATTAGGTTAGA	100507650
rs552744086	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23264301	AAAGCAAAGGTTTAT[C/G]AAGAACTTAAATTTA	100507650
rs552783154	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272992	TGTATCCCTGCATTG[C/T]TTCCTAGTTTCACTC	100507650
rs552839345	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210604	AACATAGTGAAACCC[C/T]GTCTCTACTAAAAAT	100507650
rs552861373	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251403	TTCAGACTGGCCAAC[A/G]ACAAACTTGAGGATT	100507650
rs552888781	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256876	AAATTATTTTTTGGC[C/T]GGGCATGGTGGCTCA	100507650
rs552920392	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196317	TCCGCCATTATCATG[A/C]CAAAATGCATGGCCC	100507650
rs552927533	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263850	CCCAGCACTTTGGGA[A/G]GCTGAGGCGAGTGGA	100507650
rs552965718	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223773	AGAAATAAAGGGCAT[C/T]CAAATTGGAAAGGAA	100507650
rs552995858	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23219963	CCGAGGCAGGTGGAT[C/T]GTTTGACGTCAGGAG	100507650
rs553004745	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23194159	ATATACTATCACTTA[A/C]AAATTAAAAACAAAA	100507650
rs553023065	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23248662	GGTCAGGCTAGTCTC[A/G]AATTCCTGACCTCGT	100507650
rs553046086	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23219430	ACAAAAAGTTTAAAA[A/G]CAGAGGAAAGAAGTT	100507650
rs553046872	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189200	TTCGCTTCTAGTTGA[C/T]ATCTTTGACTATTGT	100507650
rs553052733	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203278	CACTTACAATAATAG[C/T]CTCCAATCTCATCTA	100507650
rs553073562	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23232118	CATCGTCTGGGATGT[C/G]AGGAGCCCCTCTGCC	100507650
rs553085298	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23225667	GGGAAGGGTAGTGGG[A/G]ATGGGGTGGGGAGGA	100507650
rs553111360	snp	A/T	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23219753	CTGGGATTACAGACA[A/T]GAGCCACCACTCCCA	100507650
rs553159056	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220686	GAAAATTAGCTGGGC[A/G]TGGTGGCGGGCACCT	100507650
rs553210901	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23243375	AGGAAGTATATACAA[A/G]GTACAGATGATGAAT	100507650
rs553222136	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220348	ACCAGCCTGGCTAAC[A/G]TGGCAAAACCCCATC	100507650
rs553222445	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23226399	ACTTTAGGAAGCTGT[A/G]GCGGGCGGATCACCA	100507650
rs553222619	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215606	AGAAAGGAACTGTCC[A/T]TCCAGAATTCTATAC	100507650
rs553245100	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23257270	AATCCTCCTGCCTCA[A/G]CCTTGGCTTCCTGAG	100507650
rs553275720	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250862	AGGGGCTTCTAGGTC[A/T]TAGGTAGATAAGAGA	100507650
rs553288023	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200420	AACCTCTGCCTCCTG[A/G]GATCAAGCAATTCTC	100507650
rs553333140	in-del	-/T	0.00358779	0.0422022	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184272	CAGGGGAGGATCACG[-/T]TGAGCCCAGGAGTCT	100507650
rs553370340	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221874	GGAAATTAAACAGTA[C/T]GCTTCTGAATGAACA	100507650
rs553403861	in-del	-/AAAAAC	0.0416478	0.138164	intron-variant	RNF212B	GRCh38.p7	14:23220203	AACAAAAACAAAAAC[-/AAAAAC]AAAAACAAAAACAAA	100507650
rs553423140	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219702	GTCTCAAACTGCCGA[C/T]CTCAGGTGATCTGCC	100507650
rs553439862	snp	C/G/T	0.00874735	0.0655527	intron-variant	RNF212B	GRCh38.p7	14:23217258	TGGTGGCAGTGGTGG[C/G/T]GGGGGGGCTCCTCTG	100507650
rs553538150	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246874	GGCCGGGTGTGGTGG[C/T]TCACGCCTGTAATCC	100507650
rs553538296	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23191189	CAAAACTCCATCCCT[A/T]CTAAAAATACAAAAA	100507650
rs553558215	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214344	ACTAAAAATACAAAA[A/G]TTAGCTGGGCATGGT	100507650
rs553592741	in-del	-/T	0.499987	0.00259581	intron-variant	RNF212B	GRCh38.p7	14:23256376	TTCTCCACTGTTTAA[-/T]TTTTTTTTTTTTTGA	100507650
rs553611589	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240148	TTATAACAACCTGCT[A/C/G]TTATAAAAAGCAGTC	100507650
rs553679966	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216923	CAATCTCAAAGGTTA[C/T]AGATTGTATGATTCC	100507650
rs553689641	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23220622	CGAGGTCAGGAGATC[C/G]AGATCACCCTGGCTA	100507650
rs553709735	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212027	GCCACCGTGCCTGAC[C/T]AAAAAAGAAAAATTA	100507650
rs553722564	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198673	AGAAAACTCTGTCCA[-/A]AAAAAAAAAAAGGTC	100507650
rs553746682	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214897	TTCAAGAAGAATAAA[C/T]CCAAATAAATCCATG	100507650
rs553819371	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211419	GCTTCACTGGTAAGT[C/T]CTACCAAACATTTAA	100507650
rs553842377	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23254104	GGCAACATAGTAAGA[C/G]CCTTTCTCTTAAGAA	100507650
rs553849505	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197203	GTACATAAGTGGTCA[C/T]TGATGTTATCATCCA	100507650
rs553857531	in-del	-/AAAAC			intron-variant	RNF212B	GRCh38.p7	14:23254287	ATACTCTTTATCTCA[-/AAAAC]AAAACAAAACAAAAC	100507650
rs553881028	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23252350	CACCACACCCTGTTC[A/C]AAAGATCCCCCTCAA	100507650
rs553883087	in-del	-/TCAATATACATTGAATATACATTAAATG	0.0150606	0.0854603	intron-variant	RNF212B	GRCh38.p7	14:23227536	TATGTATATTATACA[-/TCAATATACATTGAATATACATTAAATG]TCAATATACATTGAA	100507650
rs553943888	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23227823	AGGCTGATCTCAAAC[C/T]CCTGGACTCAGGTGA	100507650
rs553974905	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207001	AAACATGCACACATA[C/T]ACACACACATCTTGG	100507650
rs554025557	snp	C/G	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23269535	CCAGGTGTTGGAGAC[C/G]AGGCTGAGCAACAAA	100507650
rs554036318	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206065	TATTACATAAACCTG[A/G]AAAAGCATTTGACTA	100507650
rs554109639	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199364	TTTTGAGATTCTGTT[A/G]GCCTTTCCAAAGGAG	100507650
rs554122084	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184042	TATTTAGGACTGGAT[C/T]CTGTATTTGAGAATA	100507650
rs554164355	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210424	TTTGAACAAAGTCTG[C/G]AGTTTAGTTAATTAT	100507650
rs554165583	snp	A/T	0	0	intron-variant	RNF212B	GRCh38.p7	14:23227363	TTAGAAAGCAGGACA[A/T]TGGTTGCCTTTAGGG	100507650
rs554203212	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23238010	TGAGGAGAACTGGAT[G/T]ATTTCCTGAGATCTG	100507650
rs554238271	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210012	ACAAAAATTAGCTGG[C/T]ATGATGTGTGTGCCT	100507650
rs554245780	in-del	-/AGAA	0.00478085	0.0486577	intron-variant	RNF212B	GRCh38.p7	14:23225715	CATACCAAAAAAAAT[-/AGAA]AGAATAAATAAGACC	100507650
rs554251422	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258103	CAACACTTTGGGAGG[A/C]TGAGGTGGGTAGATC	100507650
rs554345910	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232515	TGGGAAGTGAGGAGC[A/G]TCTCTGCCCAGCAGC	100507650
rs554354599	snp	A/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23245037	AAACTTTGGTTTTTT[A/T]CCTTCTACTCCCCAT	100507650
rs554363354	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221846	AGGAATTTTGGAAAG[C/T]ATATGAACACATGGA	100507650
rs554375755	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265987	TTTGTTCATTTGTGT[C/T]TTTTTTTGAGATGGG	100507650
rs554397756	snp	A/C	0.00199481	0.0315187	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273957	AAGTCCTGCCCCTCC[A/C]AACAATAAGTTAAAA	100507650
rs554508110	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265358	TTCTTTGCTGTGTTT[A/T]AAACATAAAAATATT	100507650
rs554538960	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23191518	TTGTTAGTTGGTTTT[C/T]CTAGGGGGTAATGAT	100507650
rs554544448	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265282	CACAAGATGGCATTA[A/C]AAGCTAAGTGTAAAA	100507650
rs554585438	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273883	AGAAACAACCTGGCT[A/G]GCGATAGATGCTGAA	100507650
rs554616608	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23256634	ACCTTGGTCTCCCAA[A/T]GTGCTAGGATTACAA	100507650
rs554634273	in-del	-/TA			intron-variant	RNF212B	GRCh38.p7	14:23257399	TTTAAAAAAATAGAC[-/TA]GAGTAAATTCTTATC	100507650
rs554646751	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216212	GATCGTGCCACTGCA[C/T]TCCAGCCTGGGTGAC	100507650
rs554654190	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23229813	AACCCAGACTACTAG[C/T]GCACAGCAAATAAAG	100507650
rs554686580	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23223448	GCAACCTCCGCCTCA[C/T]GGGTTCACGCCATTC	100507650
rs554727288	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23254631	ACTCCTGAGTTCAAG[A/G]TATCTGCCCACCTTG	100507650
rs554758241	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23251554	GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	100507650
rs554802891	snp	A/G	0.0134861	0.0810011	intron-variant	RNF212B	GRCh38.p7	14:23217482	TGCTGTGCTGGCTTC[A/G]TGTCTGACCCAGCAC	100507650
rs554816337	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23238752	AAATAATAATAATAA[C/T]AATAATAATAATAAT	100507650
rs554821753	in-del	-/AGAAAAAGAGG	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214765	TGTCATTGTAGTCCC[-/AGAAAAAGAGG]AGAAAAAGAGGAGAA	100507650
rs554823944	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232452	CTCCGCCCGGCAGCC[A/G]CCCCGTCTGAGAAGT	100507650
rs554825871	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226573	GAGGCGGAGCTTGCA[G/T]TGAGCCGAGATCGCG	100507650
rs554841584	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210956	AATGTTATAAACAGT[A/G]TTAAAGCAACAAATT	100507650
rs554889006	snp	C/T	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23232277	CTGGGATGTGAGGAG[C/T]GCCTCTGCCCGGCCG	100507650
rs554893787	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23246226	TGCAACCTCTGCCTC[C/T]AGGGTTCAAGCGATT	100507650
rs554906796	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23189647	TTTCTACTAAAAATT[-/A]AAAAAAAAAAAATTA	100507650
rs554912422	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205916	ATTTTGACACCTTAC[A/G]TTATTTGGCAGGGTA	100507650
rs554983958	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197586	ATAAGCAAATTAAAA[A/T]TTATTTAAAAAAACA	100507650
rs554985255	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250174	CCTGAAATGCCTGAT[G/T]TCTACACTTTAAAAA	100507650
rs554988033	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273138	ACACTGGTAGCTCCC[A/C]TCATTTCCTACAATT	100507650
rs555004492	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244161	GGTAAGGAGAATTGG[A/G]CATATAATGTACATC	100507650
rs555008274	snp	G/T	0.00159617	0.0282053	utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23237918	CACACCTCTCACACC[G/T]CCTCGGCTGCGCCCA	100507650
rs555053188	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208798	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	100507650
rs555076107	in-del	-/T	0.250168	0.25	intron-variant	RNF212B	GRCh38.p7	14:23223362	ACTGAAAGCCTTTCC[-/T]TTTTTTTTTTTGAGA	100507650
rs555127430	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241034	AGGATACTTAAATTT[C/T]AGTGTCTTTTTTTTT	100507650
rs555129676	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197083	AATTGCTGAATGAAT[A/G]TATATAGGACATGTA	100507650
rs555142922	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250737	CATGTGCCCAAGGTG[G/T]TCAGAGTACAGTTTG	100507650
rs555152229	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237423	GCGTGAGCCACCGCC[C/T]CTGGCCAAAAATTTC	100507650
rs555228825	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23252031	TGATTGATTAAAGAA[C/T]TTGTCATTGGCGATT	100507650
rs555258141	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23194117	AAAGTGCTGGGTTTA[C/T]AGGCATGAGCCACCA	100507650
rs555278412	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23234769	ATTTTCCAGTGAAAA[C/G]TTTTATTTAAGTAGA	100507650
rs555318344	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189713	ACTCAGGAGGCTGAC[A/G]TAGGAGGATTGCTTG	100507650
rs555388667	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186539	GTTTTTAGTAGAGAC[A/G]GGGTTTCACCCTGTT	100507650
rs555394879	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184869	CAGCATGAAGCAATA[C/T]AGTGGACAACACTAT	100507650
rs555484994	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240287	ACATAGATTTTGGAA[C/G]AGCTATAATTATGTT	100507650
rs555595101	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192174	CATTTGACCCAGCCA[C/T]CCTATTACTGGGTAT	100507650
rs555622231	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274725	ATCCTGGCTAACATG[A/G]TGAAACCCGTCTCTA	100507650
rs555623538	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23233239	TCATCACCACTCCCT[A/G]ATCTCAAGTACCCAG	100507650
rs555681001	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23267696	GGCCTCCCAAAGTGC[G/T]GAGGATTACAGGCAT	100507650
rs555710430	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191311	GTAGTGAGCCGAGAT[C/T]GCACTGCACCCTGGG	100507650
rs555710598	in-del	-/C	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23263344	CTTTTCACAAGCCAA[-/C]CCTGACTTTCAGGGA	100507650
rs555710715	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208790	TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC	100507650
rs555749806	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23224904	GCTCAAACAACTCTA[C/T]GGGAAAAAATCTGAT	100507650
rs555772948	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23217295	GAAAGGGGAGGGAAG[A/T]GCGGGAAGAACTTTA	100507650
rs555779929	snp	A/C	0.00914312	0.0669923	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198641	AGATCGCGCCATGGC[A/C]CTCCAGCCTGAGAAC	100507650
rs555780630	snp	A/C	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23218171	CAGGAGATCGAGACC[A/C]TCTTGGCTAACACGG	100507650
rs555792485	snp	C/T	0.000399281	0.0141238	missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23260666	ACCTATAGGAATCTC[C/T]AAGTCGGTACCAAGG	100507650
rs555802133	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23232841	GAGGTGGGGGTGCCT[C/T]TGCCCAGCTGCCCCG	100507650
rs555843382	snp	A/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274735	ACATGATGAAACCCG[A/T]CTCTACTAAAAATAT	100507650
rs555850201	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212667	GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC	100507650
rs555873388	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23264969	TAGGATTACAGGCAT[A/G]TGCCACCACGCCTGG	100507650
rs555881810	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23241185	GGAATTTGCCAAGTG[A/G]ATAAGGCAGGGAAGA	100507650
rs555948147	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222511	GTCTCCCAATAAAGA[A/G]AAGCCTGAGACCCAA	100507650
rs555955140	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223094	AAAAGATTGTTCATC[A/G]TGATCAACTGAGATC	100507650
rs555964390	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23267071	CCTTCCAGGCTTAAG[C/T]GATAGTCCCACTTCA	100507650
rs556024301	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234673	GTTTATGCACCAACA[C/T]CACACTTTAAATTAC	100507650
rs556176033	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23252994	TAAACCCTATGAGGA[C/T]GGTTTATTTTCATGC	100507650
rs556176086	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260607	GACTGAAGATCTGTT[A/G]ATTAGGATCCTCAGT	100507650
rs556218501	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213149	AACCCCGTCTCTACT[-/A]AAAAATACAAAAAAT	100507650
rs556230671	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207115	AGCTAGGACAAAATG[C/T]TGCTATTTCAGAAGT	100507650
rs556244322	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198581	CTAGGGAAGCTGAAG[A/C]GGGAGAATCACTTGA	100507650
rs556252193	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205705	ACAATAACAGTCCTT[C/T]CCCAAAACAAACCTC	100507650
rs556321803	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23264820	CATATATTACAAGGT[-/T]TTTTTTTTTTTTTTT	100507650
rs556366310	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247654	AAATGGATATACATT[C/T]TACTTATCCATTCAT	100507650
rs556384110	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191060	TGACCACCCAATAGA[A/G]AGTCCATCGCAGGCT	100507650
rs556403420	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23269490	TAATCCTAGCACTTC[A/G]GGAGGCTAAGGTGGG	100507650
rs556406725	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229625	TTTAATTTGCATTTC[C/T]CCTATGACTAATTAT	100507650
rs556425484	in-del	-/AAAAACAAAAACAAAAAC	0.0633499	0.166318	intron-variant	RNF212B	GRCh38.p7	14:23220186	CAAAACTGTCTCGGG[-/AAAAACAAAAACAAAAAC]AAAAACAAAAACAAA	100507650
rs556441046	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23228838	CTTGAATATGTATAG[A/C]ACACTGATTTTCCTT	100507650
rs556516175	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23193336	TCAGAAAGCTGTTGG[A/G]GAATGTGCACCACCA	100507650
rs556593513	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23188638	TGCCTGGCAAATTTT[A/T]AAAAAATTTTTAGTA	100507650
rs556607543	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23238114	CTGAGGCCCCATCGC[C/T]TCTGGAAAGCAGGGG	100507650
rs556649743	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221535	GACAGACTCCAATAC[A/G]GTAATAGCTGGAGAT	100507650
rs556679389	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232788	TGGGAGGGAGGTGGG[C/G]GGGGGGTCAGCCTCT	100507650
rs556731280	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189151	CTTTCCAATTACCTG[C/T]TCCTCTCTTCAAACC	100507650
rs556785381	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266205	CTCAGGTGATCTGCC[C/T]GCCTCAGCCTCCCAA	100507650
rs556846636	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184569	ACCAGGTAGCCTTGT[C/T]GTTCACAGCTCTTAT	100507650
rs556869588	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209495	GTATCTAATATTAGA[C/T]ATCCAATGTATAAAA	100507650
rs556896416	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23224850	TATATTTGCAAACTT[C/T]CCATCTGACAAGGGA	100507650
rs556897598	snp	A/C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202707	ATACAAAAAATTAGC[A/C/T]GGGCATGGTGGTGGG	100507650
rs556932409	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242362	TACTAAAATTTCACT[C/T]TACAGGGAAAGATTA	100507650
rs557003142	snp	A/C	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23262007	AAAACAAAACTCTCT[A/C]TATATATACACACAC	100507650
rs557003733	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235638	AGCTTGACAGCTTCC[C/G]AAGACTCAAATACTT	100507650
rs557035273	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223516	CCCGCCATCAAGCCC[A/G]GCTAATTTTTTTGTA	100507650
rs557042570	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209038	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC	100507650
rs557076392	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225639	GAGAATAGAAGGATG[G/T]TTATTAGAGGCGGGG	100507650
rs557077224	snp	C/T	0.0178098	0.0926698	intron-variant	RNF212B	GRCh38.p7	14:23231875	TCCAGCTCCTAACCG[C/T]GAGTGATCTGCCAGC	100507650
rs557078111	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23265929	TACTGCATCCTATAA[C/T]ATTTGGCATGCTGTG	100507650
rs557179210	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240484	ATTCAGGGAAAAATG[A/T]TTTCATGTAAGGATG	100507650
rs557181117	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23220232	AAAACAAAAACAAAA[A/G]CAAAAACCATACAAC	100507650
rs557214149	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232099	GCGTCTCTGCCTGGC[C/T]GCCCATCGTCTGGGA	100507650
rs557231569	snp	A/C	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23263755	GTGCCCCTTCCCCCA[A/C]AAAAAACGAGTGTTC	100507650
rs557263468	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256812	CCACTTCAGCCTTTC[A/G]GGTAGTTGAGATTAC	100507650
rs557297674	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200664	TCCAAGATAAATCTG[A/G]GGCTTCCGTGCCTGT	100507650
rs557356163	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23262102	ATAGAAGTTACAGTC[C/T]AATGTTCTTTTGTCC	100507650
rs557373812	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186487	CCTAAGTAGCTGGGA[C/T]TACAGGCACCTGCCA	100507650
rs557412837	snp	A/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23248608	CACCACACCTGGCTA[A/G]TTTTTGTATTTTTAA	100507650
rs557427858	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223676	TTCTTTTCAGATCTG[A/G]AATGTGATAAGAATG	100507650
rs557435017	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194256	AATTTAAGGCAAAAA[A/G]CATCAATATATATAA	100507650
rs557524673	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197192	AAGTGTTATTAGTAC[A/G]TAAGTGGTCACTGAT	100507650
rs557558759	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213698	TGTGCTCTACCTAAA[C/G]AGGGTGACTGCATGC	100507650
rs557568416	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219406	TGCAATAAAACATAA[A/G]GAGAAAGAACAAAAA	100507650
rs557571549	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194792	AGGCCAGAAAAATTA[C/G]TAAACAGATAAAATA	100507650
rs557573388	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272521	GCCTAAGAACTCTGC[C/T]TCCCTGGTAGTCATC	100507650
rs557608299	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219468	AGCGCTCTCCTTCTT[C/T]TCCTTCTAGTTTTTT	100507650
rs557619827	snp	A/G	0.00438332	0.0466095	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213245	GTGAACCCGTGAGGC[A/G]GAGCTTGCAGTGAGC	100507650
rs557653602	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187643	ATTCTTGCTTTTTGT[A/G]ACAGAGCTGGGAAGT	100507650
rs557658146	snp	A/C			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23261064	AACCTGACGCGTCTA[A/C]CTTACTGCTGTGTCC	100507650
rs557693675	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208964	GGGGTTTCATCGTGT[A/T]AGCCGGGATGGTCTC	100507650
rs557706049	in-del	-/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23240167	TAAAAAGCAGTCTGC[-/T]TTTTTTTCACTGTAT	100507650
rs557721781	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23248590	GGGATTACGGGCATG[C/T]GCCACCACACCTGGC	100507650
rs557796337	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23268977	AGGTCAGTAACACTA[C/T]GCTTCCTTTTTCTTG	100507650
rs557799954	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241105	GGGACTTGGGGTAGG[G/T]TGTTTTGATCACGGA	100507650
rs557865066	in-del	-/A	0.25214	0.249991	intron-variant	RNF212B	GRCh38.p7	14:23224235	CAAATATAGAATGTC[-/A]AAAAAAAAAAAGCTA	100507650
rs557908841	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261461	GTCTTTAAAGAGGAA[A/C]CTCCACCTTACTTTT	100507650
rs557934689	snp	G/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23234946	GGGCTGGGTACGGTG[G/T]CTCATACCTGTAATC	100507650
rs557934755	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241820	CGGGCGCAGTGGCTC[A/C]TGCCTGTAATCCCAG	100507650
rs557977747	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270177	CCTGTCACCAGTCGA[A/G]TCCTACTATTTAGCC	100507650
rs557994660	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23185676	TATGGGATCAAATAC[A/G]TTCTTGGAATACAGC	100507650
rs558009987	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23224750	AAACAAAAATGGACA[A/C]ATGGGATCACATCAA	100507650
rs558047692	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23263169	GGACATGGGCAGACA[A/G]TCATTAACAGTATAC	100507650
rs558055496	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23188487	TTTTTTAGAGATAGG[G/T]TCTCACTCTCACTCT	100507650
rs558069946	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23231838	GTGGAGAGGGGGTTT[C/T]GCTGTGTTGGCCGGG	100507650
rs558084442	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23262125	TTTTGTCCTTCTATA[C/T]TTCTGATAAGCCCAT	100507650
rs558120121	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248376	GGCTCACGCAATCTG[C/T]CCGCCTCAGCCTCCC	100507650
rs558161106	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213219	TCGGGAGGCTGAGGC[A/G]GGAGAATGGCGTGAA	100507650
rs558170198	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193058	GATCACGCCATTGCA[C/T]TCCAGCCTGGGCAAC	100507650
rs558193303	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265161	TTTGTCTTCCAACTA[A/G]TAAGGGGAAAATAAA	100507650
rs558232357	in-del	-/ATACAC	0.0138312	0.0820018	intron-variant	RNF212B	GRCh38.p7	14:23229261	TATATATATATATAT[-/ATACAC]ACCACATTGTTTATC	100507650
rs558236363	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23264687	GTGAGGTGGGGGGAA[A/C]AGGGTGTCAGAAATC	100507650
rs558268069	in-del	-/G	0.00953873	0.0683987	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198541	TCAGCTGGGCGTGGT[-/G]GGCGGGTACCTGTAA	100507650
rs558333595	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218743	TAACCTTAAAGAGGA[A/G]GTAGAGAAAGAGAGC	100507650
rs558373292	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23234411	GATTTCCTGCACACC[A/T]AGGTTATAAGAGTAT	100507650
rs558375117	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273797	GTAGCAAATGGAGTT[A/G]CCTCCAAGACTGTTG	100507650
rs558395368	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23221821	AATAAAACTAAAAAT[C/T]AATAACAGGAGGAAT	100507650
rs558398573	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23223499	TAGCTGGACTACAGG[C/T]GCCCGCCATCAAGCC	100507650
rs558452587	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250939	GGCAATCAGATATGC[A/G]TGTATCTCAGTGAGC	100507650
rs558474844	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220109	GTATCCCTTGAACCT[A/G]GGAGGCAGAGGTTGC	100507650
rs558478774	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214435	GGAGGTGGAGGTTGC[A/G]GTGAGCCCAAATTGC	100507650
rs558481699	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23194661	AATCGCATGAGCCCG[A/G]GAGATGGAGGTTGCA	100507650
rs558488688	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23226455	CTAACACGGTGGAAC[A/C]CCATCTCTACTAAAA	100507650
rs558523497	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242906	ATCACTTGAGCCCGG[A/G]AGGTTGAGGCTGCAG	100507650
rs558524852	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252019	ATTACATAGGCATGA[C/T]TGATTAAAGAATTTG	100507650
rs558546984	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212B	GRCh38.p7	14:23232256	GCCTCTGCCCCGCCG[C/T]CCCATCTGGGATGTG	100507650
rs558571776	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189675	TTAGCTGGGTGTGGT[G/T]GTGCATGCCTGTAGC	100507650
rs558574661	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194525	GGCAGATCATCTGAG[C/T]TCAGGAGTTTGAGAC	100507650
rs558580500	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242587	GTATCTTGTACTCTT[C/T]CTCACTCTTGTAAAT	100507650
rs558602768	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236912	TGTTTCATTGTTATC[C/T]AGAATGCTTCTGTGG	100507650
rs558626333	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196972	CCCCATCTAGACTGC[A/G]AACTCCATGAGTGCA	100507650
rs558630483	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189252	GGCAGAAGAGAACTT[C/T]CCCATGCTCCATTTA	100507650
rs558632112	in-del	-/AC			intron-variant	RNF212B	GRCh38.p7	14:23218620	GTCTCAAAAGAAAAT[-/AC]AGAGTCAGAGGAGAC	100507650
rs558683398	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220707	GCGGGCACCTGTAGT[C/T]CCAGCTACTCAGGAG	100507650
rs558738588	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216122	GTGGTGGCGGGTGCC[G/T]GTAGTCCCAGCTACT	100507650
rs558740060	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243467	TTGGGAGGTCAAGGC[A/G]GGTGGATCGCCTGAG	100507650
rs558769699	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23245068	TTCTCTTAGATTATT[C/G]TATAGCCTCATGGAA	100507650
rs558810840	snp	G/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237319	ATTTTTAGTAGAAGC[G/T]GGGTTTCGCCATGTT	100507650
rs558822220	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215730	AAGAATGGCTAATGA[A/T]AATTTTTCAAACAGA	100507650
rs558825404	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249310	ATACCACTTTGGAGG[C/T]CAAGGTGGGAGGATT	100507650
rs558847955	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23244013	AACCCAAAAGGCGAG[G/T]GTTGCAATGAGCCTA	100507650
rs558915592	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202837	CCTGGGCGACAGAGC[A/G]AGACCCTGTCTCAAA	100507650
rs558952662	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270545	GACCCACAAGTAACA[A/C]TGCCGAGAAACTGCC	100507650
rs558959960	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23250128	GTTCTTTGCAGTTCT[C/T]TTACAGACCATATAC	100507650
rs558991422	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203829	CCCTAGTGGCTGTAC[C/T]AGTTTACATTACCAC	100507650
rs559049175	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256697	AAATTTTCTAAAATA[A/T]TTTTTTTAAGTTGGG	100507650
rs559076694	snp	C/G	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23262676	GCAGGTCAATCACAC[C/G]TCGACCAGTGGGCAT	100507650
rs559165581	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214217	GAAAAACTAAGGCTG[A/G]GCATGGCGGCTCAAG	100507650
rs559233943	snp	C/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23220611	CAGGTGGATCACGAG[C/G]TCAGGAGATCGAGAT	100507650
rs559334162	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236518	AGACTCTGCTTCAAA[A/C]AACAACAACAACAAC	100507650
rs559355895	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23253930	TACAGATGTTCAAAA[A/G]TTAAATTGCGTGCAA	100507650
rs559375826	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209817	CATGTACCCCTGATA[A/C]AACATGATGACAGGG	100507650
rs559450686	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209290	AACCTGTTTTACCAG[C/T]AAGGTCTTTATGACC	100507650
rs559454631	snp	A/G			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194996	GATTCTTGGGTCACA[A/G]TGAAATTAAATTAGC	100507650
rs559495265	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23192078	TAGGAACATTTTTAC[A/G]CTGTTGGTAGGACTG	100507650
rs559551865	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23238397	TATCGTAAATCTTAC[G/T]AAGTTTGTATCCCTC	100507650
rs559551924	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23261489	TTTTACACTACTCAT[C/G]CTTCAAAATTGAACT	100507650
rs559588206	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249644	CTTCTGAAACAGTGT[A/C]GTTGAATTCTTCATC	100507650
rs559634284	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23257847	CAGGTGACTCTGTAG[G/T]TGTCTTTAGGGAAAA	100507650
rs559654010	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194431	GGAGAAATTTTAATG[C/T]ACCTCTATTAGAAGC	100507650
rs559660390	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243626	ACTTGAGCCCAGGAG[A/G]TGGAAGTTGCAGTGA	100507650
rs559661960	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195494	TCACTGCTCTGGAAC[C/G]AATTGTTTTGTAATG	100507650
rs559697994	snp	A/C	0.251859	0.249993	intron-variant	RNF212B	GRCh38.p7	14:23254307	CAAAACAAAACAAAA[A/C]AAAACAAAACAAAAA	100507650
rs559698022	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250237	CTAATCCCAGCACTT[G/T]TGGAGGCTGAGGGGG	100507650
rs559733216	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261603	AGGTACCATGTTACA[A/G]GCTGGATATATACCA	100507650
rs559790930	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23238396	TTATCGTAAATCTTA[C/T]GAAGTTTGTATCCCT	100507650
rs559865900	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274321	CTCTGTCAAGCTGGA[C/G]AGGAGGTAGTTAACA	100507650
rs559870801	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23251699	CGGGCGCCTGTAATC[C/T]CAGCTACTCTGGAGG	100507650
rs559911322	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23216268	CAAAAACAAAACAAA[A/G]CAAAACAAAATCTAT	100507650
rs559950645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201931	TATAACTTCCATAAA[C/T]CTTTTATAACCTTTA	100507650
rs559970582	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225651	ATGGTTATTAGAGGC[A/G]GGGAAGGGTAGTGGG	100507650
rs559971790	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23234746	CCCACTCCACATGGC[A/G]CTAAAATATTTTCCA	100507650
rs560023148	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235699	AAGTGATTTTTTATA[C/T]TGTGTAATGAACTGT	100507650
rs560023213	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23223788	CCAAATTGGAAAGGA[A/G]AAGGTCAAATTATCC	100507650
rs560033870	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274700	ATCATGAGGTCAGGA[A/G]ATCAAGACCATCCTG	100507650
rs560112226	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210587	TTGAGACCAGTCTTG[A/C]CAACATAGTGAAACC	100507650
rs560132472	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23230399	GTGGCTCACGCCTGT[A/C]ATCCCAGCACTTTGG	100507650
rs560143453	snp	G/T	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204691	TTTTTGCTTAGTCTT[G/T]CTTTGGCTATGCAGG	100507650
rs560197838	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191372	AAAAAAAAAAAAGCA[A/G]GAAAGTCCACCTCCA	100507650
rs560215188	snp	G/T	0.0182019	0.0936463	intron-variant	RNF212B	GRCh38.p7	14:23232856	CTGCCCAGCTGCCCC[G/T]TCTGGGAAGTGAGGA	100507650
rs560234879	snp	A/T	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23254897	TTAATATGCTCTCTC[A/T]AGCATATAAAATAAA	100507650
rs560306554	snp	C/T	0.0248432	0.108648	intron-variant	RNF212B	GRCh38.p7	14:23232678	GCCAGCCGCCCCGTC[C/T]GGGAGGGAGGTGGGG	100507650
rs560404148	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183679	GTGCTTCTCTTTAGC[G/T]AGGGGTTTTATTCGC	100507650
rs560451634	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220947	AAAAAAGGAAGAGAA[G/T]ACTGTAAAACAACCA	100507650
rs560540762	snp	G/T	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23257525	AGAACAAAAAGTTTA[G/T]GAGAAGAGTACCAAG	100507650
rs560542713	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23250502	AAAAAAAAAAAGACT[A/G]AATTAATAATTACCT	100507650
rs560588687	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258127	GTAGATCACCTGAGG[C/T]CGGAAGTTCAAGACT	100507650
rs560621406	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273872	TTTGATGGCTGAGAA[A/G]CAACCTGGCTGGCGA	100507650
rs560658902	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23251059	TCCAACATATTTTCC[G/T]TTGACACTACTAAAA	100507650
rs560661444	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232173	GAGGGCCTCTTCCCC[A/G]CCGCCATCCCGTCTA	100507650
rs560689342	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209050	GGCGTGAGCCACCGT[A/G]CCCGGCCTGGTTGCC	100507650
rs560694492	snp	C/G	0.000712843	0.0188657	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23264199	TCAGCGGAATCTATT[C/G]CTTATAGAGAGGCTG	100507650
rs560709055	in-del	-/TC	0.00120361	0.0245022	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200088	AAACATTTTTTTCTC[-/TC]TCTCTCTCTAGTTTC	100507650
rs560755989	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23271391	GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCACTG	100507650
rs560765849	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23187979	TAGGTCAGAAAGAAA[-/G]GAAGATGAAATGAGG	100507650
rs560820240	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215901	TTGAATTACATTGAC[A/G]CCACTAGACTGAGTT	100507650
rs560907483	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23245190	CCTCAAGATGATCCT[C/T]AGTCATTTTCTGGTT	100507650
rs560955675	in-del	-/TCT	0.177503	0.239258	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213688	TTAGGAACTGTGTGC[-/TCT]ACCTAAACAGGGTGA	100507650
rs560961400	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215222	TCATGTAAGGTGTGC[C/T]TTGCTTCTCCTTCAT	100507650
rs560987863	in-del	-/TT	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215192	TTCCCCCCACCCCTC[-/TT]TGCCTCTCCTGTTGT	100507650
rs561008649	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244655	TTAATTAATTTCTAC[A/G]ACTAAAGGTTGTTTT	100507650
rs561015463	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23232035	TGGCCTCCCAAAGTG[C/T]CGAGATTGCAGCCTC	100507650
rs561036629	snp	G/T	0.00636936	0.0560724	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197975	TACATTCTTAAGGGC[G/T]GGGGAGATTACAAAG	100507650
rs561058420	snp	A/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23238161	TCGCCTTAATCACCC[A/T]GTTCACTGCCTTTTT	100507650
rs561098317	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23223441	GCTCACTGCAACCTC[C/T]GCCTCACGGGTTCAC	100507650
rs561103006	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204114	GTTCGTTGTAGATTC[C/T]GGATATTAGTCCTTT	100507650
rs561110992	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197388	AAAAATTAGCCATGT[A/G]TGGTGGTACATGCCT	100507650
rs561194131	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236822	TGCTTTTTGCCAGTG[G/T]CCTTTATACCTGAAC	100507650
rs561195544	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232388	CCCCATCTGAGAAGT[A/G]AGGATCCCCTCCGCC	100507650
rs561237455	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190054	ATCTTATTGATCTTA[C/T]GGCAGCATGTGGCCA	100507650
rs561308496	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202953	ACTCAATGTTACAAG[C/G]ACTTTATTTTATTTC	100507650
rs561316691	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242697	GGGCAGGAGGTGCTG[A/G]GGTGGTGGCTCATGC	100507650
rs561365857	snp	A/C/G			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274698	GGATCATGAGGTCAG[A/C/G]AGATCAAGACCATCC	100507650
rs561366351	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271698	GAAGTAACATTCCTC[C/G]CTAAAATCCTCAAAT	100507650
rs561382193	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207242	TGGTAAATGCTAACT[G/T]TAGTCATTTAAAAGG	100507650
rs561443064	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195852	TAAACGTTGTTTTGC[A/C]TTTTACAAAGGAGGA	100507650
rs561446551	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242664	CACAGAAGAAAATTG[A/G]GAATTTATAAAAAGA	100507650
rs561494945	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23272622	TATCACCATAAGCTA[C/T]TGAAATGTTCCAGAG	100507650
rs561505773	snp	A/C	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23188921	ATGTTGATGTACATT[A/C]ATGCATAATAAATAA	100507650
rs561548666	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229707	AAATGTCTATTCAAA[C/T]CTTTTGCCTATTTTT	100507650
rs561563140	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23251352	CTGCCCCGACTCTGG[A/G]CACCAGCCACAAATG	100507650
rs561626860	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23267070	ACCTTCCAGGCTTAA[C/G]CGATAGTCCCACTTC	100507650
rs561628887	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23192819	CTTTATGGCCAGGTG[C/T]GGTGGCTCATGCCTG	100507650
rs561633770	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226026	AAAACTCGGCTGGGC[A/G]CGGTGGCTCACGCCT	100507650
rs561658541	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23233497	TTAGGAGGCTGAGGT[A/G]GGAGGATCAGTTGAG	100507650
rs561693839	in-del	-/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23222204	TGAAACAGAAAAAAA[-/G]TTCTTTTGAAAAGAT	100507650
rs561704557	snp	A/T	0.00119737	0.0244387	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274658	CATGCCTATAATCCC[A/T]GCACTTTGGGAGGCC	100507650
rs561766674	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23227603	ATCGAACAAAAAGTG[-/T]TTTTTTTGTTTGTTT	100507650
rs561790535	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274175	TCCCAACTGATGAAA[A/G]CCATTCTAAAACATC	100507650
rs561814030	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218303	AACCTGGGAGGTGGA[A/G]GTTGCAGTGAGCCAA	100507650
rs561856432	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23261023	GCCACGAGAGTACAC[C/T]GAACAAAGGAGACAG	100507650
rs561860883	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184227	AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	100507650
rs561902350	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185198	GGAGGAACTTCCTCT[A/C]CTCCTTTTGCTAGTT	100507650
rs561944190	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23259003	CCTGGGCAACACAGC[A/G]AGACTCTGTTTCTAA	100507650
rs561956906	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23193393	GAAGACCCTGAGTTC[A/G]GGAATAAGGTACCAC	100507650
rs561964418	snp	A/C	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23267363	CTCTATTGTTAGATG[A/C]ACATATAAATGTTTC	100507650
rs562042989	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212234	CTAACACAAGGATGT[C/T]TGCCTTCACCACTTC	100507650
rs562058016	in-del	-/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23257806	TGTGCCTCTCCACCC[-/T]TTCCTATAGCAGCAT	100507650
rs562067182	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23227719	ATTCTCCCACCTCAA[A/C]CTCCTTAGTAGCTGG	100507650
rs562139723	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23238507	CCAAGGAAGGAGGAT[C/T]GTTTGAGTCCAGGAG	100507650
rs562159159	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216976	TAAAATTATAGAACT[A/G]GAGAGCAGATTAGTG	100507650
rs562159679	snp	A/G			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199639	TATTCCTAGACAGGT[A/G]GGTCCCGAACGAAGA	100507650
rs562176614	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211501	AGGAATAGTTCCCCA[A/G]TGATTCTTAGAGGTC	100507650
rs562181735	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259258	GATTCACACTGATAA[C/T]ACTCATTGTAGCCTC	100507650
rs562198332	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220642	CACCCTGGCTAACAC[A/G/T]GTGAAATCCCATCTT	100507650
rs562198951	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23239642	CTTTTTTTTTGAGAC[A/G]GAGTCTGGCTCTGTC	100507650
rs562205645	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23228186	GCGGTGAGCTGAGAT[C/T]GTGCCATCACACTCC	100507650
rs562215485	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232883	AGGAGCCCCTCTGCC[C/T]GGCCACCACCCCATC	100507650
rs562247479	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203508	TTTTGAGATGGAGCC[G/T]TGCTCTGTCACCCAC	100507650
rs562250893	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221702	ATTCTTCTTTTTAGC[A/G]CATGGGTAATTCTTA	100507650
rs562275830	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23238994	ACTGAATATCAGGTA[A/C]CTCTTTTGAAAAATG	100507650
rs562339664	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247011	CAGGTGTGGTGGCAC[A/G]TGCCTTTAATCCCAG	100507650
rs562351243	snp	A/T	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23233367	CCTATGACCCTGCCA[A/T]ATGCCCCTCTGCGAG	100507650
rs562360434	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23239102	GGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG	100507650
rs562375914	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253174	TAGGAACTTTTTTCT[G/T]AAATATAACCACATC	100507650
rs562429186	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23256333	CCATTTTAGGTAATT[C/T]CCAGGATTCAGAGTG	100507650
rs562450903	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198858	AAGAGAAGTAACATA[C/T]AAGCAAGGAGGGAAA	100507650
rs562462663	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23250218	GCCGTGGTGGCTCAC[A/G]CCTCTAATCCCAGCA	100507650
rs562463061	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271268	ATATGGTAAAACCCC[A/G]TCTCTCTCTACTGAA	100507650
rs562464155	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23227997	GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	100507650
rs562487644	snp	A/C	0.00199481	0.0315187	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274730	GGCTAACATGATGAA[A/C]CCCGTCTCTACTAAA	100507650
rs562512031	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189960	CACCTTGTGGAATCC[A/C]TTGTTGTCAAGGTCA	100507650
rs562520961	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243209	AAGTCTTTAAATCTT[A/T]CCTCATGCTCATGAG	100507650
rs562537455	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205337	TTTTTTAAGCAAGAA[C/T]GTTTTCCTACAATAT	100507650
rs562587009	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197276	TCACGCCTGTAAGCC[C/T]GGCACTTTGGGAGGC	100507650
rs562589309	snp	C/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184963	AGTGGGCCTAAAAAA[C/T]TAAGTTCCCCCAAAC	100507650
rs562662670	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23267230	CAAGCAATCCTCCTG[C/T]CTCAGCTCCCAAAGT	100507650
rs562663632	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266497	GCTCACCGCAACCTC[C/T]GCCTCCCAGGTTCAA	100507650
rs562701170	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216405	AAACAGAGGAACATA[C/T]AGAAAACAAAGAATC	100507650
rs562710380	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23228543	TGGGAGGATGAGCAG[C/G]GAGGATGAGCAGGGA	100507650
rs562747596	snp	C/G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199645	TAGACAGGTAGGTCC[C/G/T]GAACGAAGATTTTTA	100507650
rs562751240	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274719	AAGACCATCCTGGCT[A/G]ACATGATGAAACCCG	100507650
rs562828517	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23227600	TTAAATCGAACAAAA[A/G]GTGTTTTTTTGTTTG	100507650
rs562837406	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23216933	GGTTACAGATTGTAT[A/G]ATTCCACTTATACAA	100507650
rs562878403	snp	C/T	0.0240643	0.107019	intron-variant	RNF212B	GRCh38.p7	14:23232327	AGGAGCGTCTCTGCC[C/T]GGCTGCCCTGTCTGA	100507650
rs562914629	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206531	CAGCAGTACATTTTA[C/T]ACATTTATAAAGACC	100507650
rs562964716	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221572	ACTCCATTTTCAGCA[C/T]TGGACAGATCTCCCA	100507650
rs562986139	snp	A/G	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23264925	CTCCCATGTTCAAGC[A/G]ATTCTCCTGCCTCAG	100507650
rs562990639	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23194337	CTTGAACTTCTAAGT[A/G]CCTAAAAATAAGGCT	100507650
rs563009836	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252358	CCTGTTCAAAAGATC[C/T]CCCTCAAAATCAGCC	100507650
rs563104975	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23257803	TTCTGTGCCTCTCCA[C/T]CCTTTCCTATAGCAG	100507650
rs563139691	in-del	-/TT	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23258856	AGAGGCCCTCCTCAC[-/TT]TTTATAGTTTTCCTC	100507650
rs563241634	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214463	TGCGCCAATGTACTC[C/T]GGCCTGGGCAACAGA	100507650
rs563280203	snp	A/G	0.0240643	0.107019	intron-variant	RNF212B	GRCh38.p7	14:23230584	GCGTGAACCCGGGAG[A/G]CGGAGCTTGCAGTGA	100507650
rs563295681	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23241998	GAGGCAGGAGAATGG[C/T]GTGAACCCCGGAGGC	100507650
rs563338117	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253332	GTTATTATGTCTCTT[A/T]AGTTTCTTTTACACT	100507650
rs563338244	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260859	ATCTTAATTGTAATG[C/T]TCACCCTGGATTGTC	100507650
rs563377316	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260415	TCTCACCAGAGACTC[C/T]GTATTTCCCCACATA	100507650
rs563392711	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23261755	TCATGGGGTCAGGAG[A/G]TTGAGACCGTTCTGG	100507650
rs563407368	snp	C/G	0.0209421	0.100162	intron-variant	RNF212B	GRCh38.p7	14:23242220	GACCTTTTAAAGTTC[C/G]CTAATGTAAAAAGCT	100507650
rs563420759	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270346	TCTTGCTAAGAGGCT[G/T]CCATCTTCCATAGCT	100507650
rs563440681	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23224691	CCAGGACACTGGTCC[A/G]GGCAAAAATTTCTTG	100507650
rs563446833	snp	A/G	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23253864	AATGTCAAAGAGATC[A/G]TGAATTTACCAATAT	100507650
rs563469109	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255388	AGCATGAAGACCATG[A/T]TATCCTTACCTGGTC	100507650
rs563493623	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259293	TCCTGGGCTCAAGCA[A/G]TCCTCCCACCTCAGC	100507650
rs563547989	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23227946	AAAAATCTCATCAGG[C/T]AATGCCAGGCATGGT	100507650
rs563630005	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218247	GTGGCACACACCTGT[A/G]GTCCCAGCTACTCAG	100507650
rs563691256	snp	C/T	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23263589	ACGAATTTGTTTTTT[C/T]ATACCACAAGGCTTT	100507650
rs563696997	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23217636	GTCTCTGCTTGGTAA[C/T]CCATAGAATTCTTCC	100507650
rs563736647	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	RNF212B	GRCh38.p7	14:23268070	GGCAGCCAAACAAGT[A/G]CTTCTAATTGTTTTC	100507650
rs563761900	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208294	TGGACGAGAAGATCA[C/T]TGGAGGCCAGGAGTT	100507650
rs563772752	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192882	GGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG	100507650
rs563799863	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23257965	TGAAAAACAGTTTTA[A/G]AAAAAATCTCTCTTC	100507650
rs563886070	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23248430	AGCCACCACGCCCAA[A/C]CCCAAGCCTCTTTTT	100507650
rs563929432	in-del	-/G	0.0166325	0.0896639	intron-variant	RNF212B	GRCh38.p7	14:23232830	CCCTGTCTGGGAGGT[-/G]GGGGGTGCCTCTGCC	100507650
rs563941709	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23235017	AAGAGTTTGAGACCA[C/G]CCTGGCCAACATGGT	100507650
rs563961740	snp	C/G	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23218359	GGTGACAGAGTGAGA[C/G]TCTATCTCAAAAAAA	100507650
rs563963372	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23223590	TCGATCTCCTGACCC[C/T]GTGATCTGCCCGCCT	100507650
rs564002923	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234415	TCCTGCACACCTAGG[C/T]TATAAGAGTATTTAC	100507650
rs564036072	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186044	GGTTGAGGCTGCAAT[A/G]AGCCAAGATCGCACC	100507650
rs564052937	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241349	GAAGTAGGCAGTGTC[A/G]GATGATGGAAGGCTC	100507650
rs564055386	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266297	TTTTGTTTTTTGGAC[C/T]CATTGGTTGTTTATC	100507650
rs564073649	in-del	-/TCTC	0.0103356	0.0711407	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200085	CTTGAAACATTTTTT[-/TCTC]TCTCTCTCTAGTTTC	100507650
rs564228647	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254372	GGGCATGGTGGCTCA[C/T]TCCTATAATCCCAGC	100507650
rs564298713	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269341	CTCTGCCAGCAGTCC[C/T]GGGATTACTTCTCCA	100507650
rs564369321	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23255318	ATCTTTAAACTAAAT[C/T]TGTTGTAATTTTGTA	100507650
rs564372829	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184274	AGGGGAGGATCACGT[A/G]AGCCCAGGAGTCTGA	100507650
rs564387234	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23253240	ATCAGTCCCCATTCA[C/T]ATTTCTCCAGTTGTC	100507650
rs564433534	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199724	AGGGAGAAAAAACAA[C/T]AACAAACAAAAGAAC	100507650
rs564445899	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23220455	AAGAATTATTGGAAC[C/T]CAGGAGATGGAGGTT	100507650
rs564474735	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222207	AACAGAAAAAAAGTT[A/C]TTTTGAAAAGATGAA	100507650
rs564478340	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207320	CTCAGGCTGTAGACT[A/G]CTCTCTACTATTCTA	100507650
rs564493885	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259292	CTCCTGGGCTCAAGC[A/G]ATCCTCCCACCTCAG	100507650
rs564532758	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256300	TTATCTCTGTTGCTC[C/T]TCACTCCTACCCCCC	100507650
rs564551694	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23217534	ATGGGTGCTTGCATC[G/T]CCACACCCACAGCTC	100507650
rs564583022	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23238097	TGAGAAGCTTGAGAC[A/G]GCTGAGGCCCCATCG	100507650
rs564584772	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211737	AATTAGTATTATTAT[A/T]TTTGAGACAGAGTCT	100507650
rs564648600	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247077	CCTGGGAGGTGGAGA[C/T]TGCGGTGAGCCAAGA	100507650
rs564775564	snp	G/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23233507	GAGGTGGGAGGATCA[G/T]TTGAGCCCAGGAGTC	100507650
rs564794147	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208202	GGGTCAAGGAAAGCA[C/T]GAGATGAGTGTGGCA	100507650
rs564807812	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247998	TGGGAAGTTCAACAT[A/C]AAGGCACTAACAGAT	100507650
rs564809670	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23239894	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG	100507650
rs564826153	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209342	TCATCCTGTGACTTA[C/G]AATGCCTTAACCATC	100507650
rs564827175	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214627	GGATAGGATCAATAA[C/G]AGAATGAATAAAGCA	100507650
rs564832410	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249772	TGGGCTGCTGTGGCT[C/G]TCATCCAGAGTGGGT	100507650
rs564841717	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196687	TCTCAAGCAATCCTC[C/T]TGCCTAGGCCTCCTA	100507650
rs564884101	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258037	CTATGGTAGAATATT[C/G]TCATTAAGATAGTAA	100507650
rs565010299	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235821	GATGTTACAAAATCG[G/T]GCATGGGCAAAAGAT	100507650
rs565041141	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204016	GTTTGCCATTTGTAT[A/G]TCTTCTCTTGAGAAT	100507650
rs565074051	snp	C/T	0.000263019	0.0114648	intron-variant	RNF212B	GRCh38.p7	14:23244317	GTGTATTGCTCTCTT[C/T]GTAGCTGAAGCCTCA	100507650
rs565077718	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242169	AGTCAAGTTAAGTAG[A/C]CTCAGGGGAAGGTTT	100507650
rs565147183	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232183	TCCCCGCCGCCATCC[C/T]GTCTAAGAAGTGAGG	100507650
rs565211997	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237013	CCCTCAACCAGGTTG[A/G]AGTGCAGTGGCGTGA	100507650
rs565238359	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208977	GTTAGCCGGGATGGT[C/T]TCGATCTCCTGACCT	100507650
rs565259178	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248738	AGCCATCACGCCCGG[C/T]CCCCAAGCCTCTTTT	100507650
rs565347445	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231646	CTCCCCTCTCCCCAC[G/T]GTCTCCCTCTCCCTC	100507650
rs565357447	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208531	AATCTGAAAGTGCTC[C/T]TCCATGGCCAAAGCT	100507650
rs565439797	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23186445	ACCTCTGGCTCCTAG[G/T]TTCAAGTGATTCTCC	100507650
rs565456481	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23253161	TATCTCTAAAAGATA[A/G]GAACTTTTTTCTTAA	100507650
rs565489048	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23224251	AAAAAAAAAAAGCTA[C/T]CCTAAAATTTGTATG	100507650
rs565555926	snp	C/T	0.00438332	0.0466095	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209004	ACCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAG	100507650
rs565559564	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225143	TGGCTTTTATTCAAA[A/T]GTCAGGCAATAACAA	100507650
rs565584985	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23188822	GGCAAAGACCTGCTT[G/T]GCTCACTGCTGTAAC	100507650
rs565586173	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271531	TTGGGTTTTGAGCAT[A/T]TTTAGGCTCCTTTTT	100507650
rs565618701	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23231915	CCGAGGTGCCGGGAT[G/T]GCAGACGGAGTCTCG	100507650
rs565660456	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23254692	AGCCACTGCACCTGG[C/T]CTAGTTTTATAAACA	100507650
rs565692044	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194660	GAATCGCATGAGCCC[A/G]GGAGATGGAGGTTGC	100507650
rs565781451	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23248588	CTGGGATTACGGGCA[C/T]GCGCCACCACACCTG	100507650
rs565796364	in-del	-/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237898	CATACCGCCAGGCCC[-/G]CGCCCACACCTCTCA	100507650
rs565810955	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213580	CTAAACTTCCACCCC[A/G]ACTCGGCAGCAAGAA	100507650
rs565854309	snp	A/T	0.0248432	0.108648	intron-variant	RNF212B	GRCh38.p7	14:23242223	CTTTTAAAGTTCGCT[A/T]ATGTAAAAAGCTGTT	100507650
rs565955328	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195433	CTTCACCATATCTCT[G/T]GTCTACCTCTAAGGC	100507650
rs565978346	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23235926	CCCACTTTGCAATCA[A/G]CTTTTAACTCAGACT	100507650
rs566014451	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258126	GGTAGATCACCTGAG[G/T]TCGGAAGTTCAAGAC	100507650
rs566016325	snp	A/C/G			intron-variant	RNF212B	GRCh38.p7	14:23234032	AACCTGGGAGGCAGA[A/C/G]GTTGCAGTGAGCTGA	100507650
rs566025444	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23230773	ATTTAGGTCTTTGAT[A/C]CATTTTGAGTTAATT	100507650
rs566036822	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23190223	TCCCATGGCTTTCAG[C/T]AGCAACTCTATACTG	100507650
rs566038723	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23193045	TGCTGTGAGACGAGA[G/T]CACGCCATTGCACTC	100507650
rs566049361	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269542	TTGGAGACCAGGCTG[A/T]GCAACAAAGTGAGAC	100507650
rs566093593	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207688	CCAAAATGCGAATCC[C/T]GAAAATTTGAGACAG	100507650
rs566117190	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234546	GATGGCTATTCAGTT[A/G]TCCCAATTCTATGTA	100507650
rs566130075	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23229487	TTCCAAAGCAGGTGC[A/C]TCATTGTACATTCCC	100507650
rs566176551	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240670	TATTACTTGAGGACT[A/T]GAATGTACTCGTTAG	100507650
rs566206365	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23273015	TTTCACTCTGTACCT[C/T]ATGCTCCCCCCATCT	100507650
rs566206807	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218594	AGCCTGGGTGACAGA[A/G]GTGAGATGCTGTCTC	100507650
rs566237278	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186224	TTTGTGACATAAACT[C/G]TTAAGTGTGTCAAAA	100507650
rs566245044	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208476	TCTAGAATGGGTGAC[A/G]GAGTGAGATCCTATC	100507650
rs566258817	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261328	GGAGCTAAGAACATA[A/T]AGTACATTGATTTCT	100507650
rs566264624	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229993	ATCTTCTCCAATGTC[C/T]CCTTTTAAAGTTGTA	100507650
rs566266380	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237814	CGCGAGCCGCTCCTA[G/T]CCCAGTGACAGCCTC	100507650
rs566271396	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23194054	ACCATGTTGGCCAGG[C/T]TGGTCTGGAACTCCT	100507650
rs566286559	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23265116	GTGAGCCACTGTGCC[C/T]GGCCTACAAGTTTTT	100507650
rs566304897	snp	A/C/G	0.00199481	0.0315187	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274704	TGAGGTCAGGAGATC[A/C/G]AGACCATCCTGGCTA	100507650
rs566317807	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23190470	TGGAGTCAACCTTGA[C/G]TTATCTTTTTCTCAT	100507650
rs566340103	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223644	ACAGGCGTGAGCCAC[C/T]GCGCCCGGCCAAGCC	100507650
rs566360776	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23188694	AGGCTGATCTCAAAG[C/T]CCTAGCCTGAAGAGT	100507650
rs566367706	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273631	AGCAAAAATACTGGA[A/G]AAACAGAAAATAGCA	100507650
rs566374009	in-del	-/GT	0.00358779	0.0422022	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204479	GCCATTTATTAAAAA[-/GT]GTCCTTTCCCCACTT	100507650
rs566385595	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214455	GCCCAAATTGCGCCA[A/G]TGTACTCCGGCCTGG	100507650
rs566419240	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232405	GGATCCCCTCCGCCC[C/G]GCAGCCGCCCTGTCT	100507650
rs566422424	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213173	AAAAAATTAGCCGGG[C/T]GTGGTGGCAGGCGCC	100507650
rs566443208	snp	A/G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23265721	CATTTCAAAGAATTC[A/G/T]TTTTGTTGAGAGTCT	100507650
rs566461482	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237281	ATTACAGGTGCGTGT[C/T]GCCACACTCGGCTAA	100507650
rs566490463	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203762	GGATTACAGGCATGA[A/G]CCACCATGGTAGGCC	100507650
rs566544781	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226401	TTTAGGAAGCTGTGG[C/T]GGGCGGATCACCAGG	100507650
rs566591547	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23220057	GACATGGTGGCACAT[A/G]CCTGTAATCCCAGCT	100507650
rs566598663	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23232253	AGCGCCTCTGCCCCG[C/G]CGCCCCATCTGGGAT	100507650
rs566652265	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225462	CTTATATACAGTAGA[A/G]TACTATTCAGCCATA	100507650
rs566652325	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219712	GCCGACCTCAGGTGA[C/T]CTGCCTGCCTCAGCC	100507650
rs566699886	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193991	GGATTACAGGAGCCT[A/G]CCGCTACGCCTGGCT	100507650
rs566724705	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189013	CCTGTACAGGGGCTG[A/G]AACACAGAGAAGAAA	100507650
rs566738255	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221727	TTCTTAAGGATAGAC[A/G]ATATGTTAGGTCACC	100507650
rs566740981	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232045	AAGTGCCGAGATTGC[A/G]GCCTCTGCCCGGCTG	100507650
rs566825657	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23243417	GAAAGAAAAGAAGAC[C/T]GGGCGTGGTGGCTCA	100507650
rs566833583	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241036	GATACTTAAATTTCA[C/G]TGTCTTTTTTTTTAA	100507650
rs566892699	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23188430	CTTCCCCTTCTTAAT[C/T]GGTTTTCATTATGTT	100507650
rs566903408	in-del	-/CAAT			intron-variant	RNF212B	GRCh38.p7	14:23224795	GCACAGCAAAGGAAA[-/CAAT]CAACAAAGTGAACAG	100507650
rs566998020	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23188723	GTTCCTCCAGCCTCA[A/G]CTTCCCAAAGTGCTG	100507650
rs567003078	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260747	CCTGTTCTTTCTTGA[C/T]TCCTGGCTGTGTGAA	100507650
rs567041537	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23246909	ACTTTTGAAGGCCAC[A/G]GTGGGTGGATCACCT	100507650
rs567078862	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256617	CCTCAAGTGATCTGC[C/T]CACCTTGGTCTCCCA	100507650
rs567087077	snp	A/C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23189582	CCAAGGCGGGAGGAT[A/C/T]GCTTGAGTCCAGGAA	100507650
rs567093894	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215315	AATCTCTTTTCTTTA[C/T]AAATTTCCCAGTTCT	100507650
rs567149308	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189187	CACACCCCAAATCTT[C/T]GCTTCTAGTTGACAT	100507650
rs567204724	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203239	AGAACATATGATGTT[C/T]GGTTTTCCATTCCTG	100507650
rs567207665	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273545	ACTGAGATCAAACAT[A/G]TATTCTACTTTGGGT	100507650
rs567274704	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183501	GTTTCCACCTGCTTT[A/G]GGTTTCTTTTCCCTT	100507650
rs567312356	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230936	GACCATAGATGTGAG[A/G]GTTTATTTCTGGATT	100507650
rs567314838	in-del	-/G	0.177503	0.239258	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213700	TGCTCTACCTAAACA[-/G]GGTGACTGCATGCCA	100507650
rs567324334	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232100	CGTCTCTGCCTGGCT[C/G]CCCATCGTCTGGGAT	100507650
rs567386545	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196795	CTAGAGGCTTCTCTT[C/T]GCCCTTAGCCTAGTT	100507650
rs567426248	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272951	TGTAGCTTCCAGTAC[A/G]CATTAGGGGTGATGG	100507650
rs567451648	snp	G/T	0.0123036	0.0774623	intron-variant	RNF212B	GRCh38.p7	14:23231743	GCAACCTCCCTGCCT[G/T]ATTCTCCTGCCTCAG	100507650
rs567520174	snp	C/T	0	0	intron-variant	RNF212B	GRCh38.p7	14:23220655	ACGGTGAAATCCCAT[C/T]TTTACTAAAAATACA	100507650
rs567523679	snp	C/T	0.000123343	0.00785214	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270008	CTTCAACTATAGACA[C/T]ATATACTAAAATGAA	100507650
rs567535592	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226968	TTTCTTGATTGTGGT[G/T]GTGGCCTCACAAATC	100507650
rs567536587	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23264503	GATCTTTCTTTGACT[A/G]GTATGCCCACTGCAG	100507650
rs567560518	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23268751	GAGAGGAAAGCACCT[A/C]TAAGAGATACTGCTA	100507650
rs567595923	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23226368	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	100507650
rs567622303	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272060	GAAATAAAAGATTGG[C/T]CATTAATTATTTGTT	100507650
rs567641190	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23249136	GATTTTTGAAGTCAT[A/G]TGTTTTTACTAATAT	100507650
rs567685192	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223723	TTATTCAACATAGGA[A/C]TGGAAGTCTTAGCTA	100507650
rs567715075	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23224378	TAAAGTAACCAAAAC[A/T]GCATGCTACTAGCAT	100507650
rs567720645	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263583	ATAAAAACGAATTTG[G/T]TTTTTCATACCACAA	100507650
rs567766067	snp	A/C	0.00835141	0.0640778	intron-variant	RNF212B	GRCh38.p7	14:23219210	GTTCTTCAATCTGAA[A/C]GAAAAAGATGCTAAT	100507650
rs567813390	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23243102	ACAGAGCTTAAGTTG[A/G]TGTCCTTTTATAACA	100507650
rs567817167	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229021	AAGCAATTACTTCCT[A/G]TCTCTCATACCCCTA	100507650
rs567848161	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23240139	TATAAAATGTTATAA[C/T]AACCTGCTGTTATAA	100507650
rs567852686	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219631	CGTGCACCACCATGC[A/C]CAGCTAATTTTTGTA	100507650
rs567863379	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23187140	GTTTCAGCTGTTTTG[C/T]GTGCTTCAGATCAGA	100507650
rs567876063	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252872	GCAAATGGTCAGCAT[C/G]TAGTGTGATGTGACT	100507650
rs567897847	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23262886	GCAAGGCAGGCATAC[C/T]ATTGATGGCAACTTT	100507650
rs567905379	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23219981	TTGACGTCAGGAGTT[C/T]GAGACCAGCCTAGCC	100507650
rs567938392	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209040	TGGGATTACAGGCGT[C/G]AGCCACCGTGCCCGG	100507650
rs567993769	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23248961	CTACCCAACTCTGCT[A/G]TTGTAGCATGGAAGC	100507650
rs567999715	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214314	GCCTGGCCAACATAG[C/T]GAAACCCCGTCTCTA	100507650
rs568001501	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266012	GATGGGGTCTCACTC[G/T]GTTGCCCAGACTGGA	100507650
rs568034906	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183873	CTTGCAACCAAGTGG[A/T]AGTAAACTCCTTCCA	100507650
rs568037129	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23253450	TTGTACCTATGGAGT[A/C]ATTTCATATGTTCCT	100507650
rs568037864	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23232930	CAGCTCATTGAGAAC[A/G]GGCCATGATGACGAT	100507650
rs568062689	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209793	ATCATCAGTTAGATA[A/T]ATGGATATCATGTAC	100507650
rs568079036	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266682	TCCCAAAGTGCTGAG[A/G]TTACAGGCGTGAGCC	100507650
rs568168443	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23217210	TAACATCAGCAGTGG[C/T]CTGGCAGAACCACCA	100507650
rs568191187	snp	A/C	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210699	GGAGAATTGCATGAG[A/C]CCAGGAGGTGGAGGT	100507650
rs568229059	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237239	GGTTCAAACGATTCT[C/T]CTGCCTCAGCCTCCT	100507650
rs568287871	in-del	-/TGTCGTCT			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204877	ATTTTCATTTGTTTC[-/TGTCGTCT]ATGATTTCTCTCAGC	100507650
rs568302033	snp	A/G	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211920	TTTAGTAGAGACAGG[A/G]TTTTGCCATGTTGGC	100507650
rs568321373	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212505	ATAACAGAAAAATCA[A/G]TTGTACTTCTACACA	100507650
rs568330773	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211091	GTCGTGATGGCGTAC[A/G]CCTGTAATCCCAGCT	100507650
rs568338561	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23252093	ATTGTCAGGGGTTGG[-/T]GGGGCGTGGGAAGAA	100507650
rs568339561	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206909	AGAAAAACAAACTTT[C/T]GTTAAAAAAAAAAAG	100507650
rs568372811	snp	A/G			missense, synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270611	TCAGCTCAGAGGGAG[A/G]GCACAACTACACTAG	100507650
rs568508289	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23232444	AGGAGCGCCTCCGCC[C/T]GGCAGCCGCCCCGTC	100507650
rs568526632	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210146	TAGAGTGAGACTGTC[C/T]CAAAACACGAACAAA	100507650
rs568553478	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207932	GACTCTAAGCGGAGA[C/G]GGGGCTTCCAGGTCA	100507650
rs568564076	snp	C/G/T			intron-variant	RNF212B	GRCh38.p7	14:23194446	TACCTCTATTAGAAG[C/G/T]TGATAAATCAGCCAG	100507650
rs568590870	snp	A/T	0.00358779	0.0422022	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197593	AATTAAAAATTATTT[A/T]AAAAAACAAATATAA	100507650
rs568591615	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23224227	CATTCTCCACAAATA[C/T]AGAATGTCAAAAAAA	100507650
rs568613260	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23232726	CCAGCCGCCCCGTCC[A/G]GGAGGGAGGTGGGGG	100507650
rs568616568	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23237934	CCTCGGCTGCGCCCA[G/T]CCTCTTTCCTCACCC	100507650
rs568628381	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23223127	AGGGATGCAAGGATG[A/G]TTCAGATATGCAAAT	100507650
rs568642845	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232709	GGTCAGCCCCCGCCC[A/G]GCCAGCCGCCCCGTC	100507650
rs568667505	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23258720	TTTTTTTTCTAAGAA[A/G]TGACAGTCCTTATTG	100507650
rs568674124	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244967	GAGCAACAGGAATGT[A/C]GAAGAAGGTAGAGAG	100507650
rs568805875	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198341	ATTCCTTGGTATCAA[C/T]TAATATCCAGTTTAT	100507650
rs568845284	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274473	CACCTCCAATAAATA[C/T]CCATTCTAAATTATT	100507650
rs568878772	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23263886	TGAGGTCAGGAGTTC[A/G]AGACCAGTGTGGCCA	100507650
rs568905898	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197459	TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC	100507650
rs568951782	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23246533	TACTTATCCTACTTC[C/T]TGTAAAGATCCAATG	100507650
rs568977526	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190785	AAACCCTCCAACGCT[A/G]CCTGTCACAGCTAAC	100507650
rs569005342	snp	A/G			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194910	ATGGTATATTTAAAA[A/G]CATTTCGATTTACTG	100507650
rs569114770	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183832	ATTTCTTTTTGCAAT[C/T]GTCTCTCGCTTTCTC	100507650
rs569158019	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214704	AAAATAGAGAGAAAA[C/T]GGGCATAACTAATGT	100507650
rs569159797	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23217135	CCCTGCCCTGAAGGG[A/T]GAGTCTTAGGCCTGG	100507650
rs569165457	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237899	CATACCGCCAGGCCC[C/G]GCCCACACCTCTCAC	100507650
rs569192350	in-del	-/G	0.0244538	0.107838	intron-variant	RNF212B	GRCh38.p7	14:23222823	TTGGGAGGCTGAGGC[-/G]GGGGGGATCATCTGA	100507650
rs569202767	snp	C/T	0.000245851	0.0110845	missense, utr-variant-3-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23272838	ACTCTCTACCAACAA[C/T]GGAGGCATATGGGAT	100507650
rs569222796	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23234674	TTTATGCACCAACAC[C/T]ACACTTTAAATTACA	100507650
rs569228312	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237360	GTCTATAACTCCTGA[C/G]CTCAAGTGATCCGCC	100507650
rs569234090	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23264307	AAGGTTTATCAAGAA[C/T]TTAAATTTATATTGG	100507650
rs569234230	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23256716	TTTTAAGTTGGGCTG[C/T]TGCTCTGTTGCCCAG	100507650
rs569273424	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199996	AGAATTCAGCCCAAA[C/G]TGTAGAACATAATAA	100507650
rs569275216	in-del	-/A	0.229136	0.249128	intron-variant	RNF212B	GRCh38.p7	14:23221233	TCTACTGAAAATAGG[-/A]AAAAAAAAAAAAAAA	100507650
rs569353393	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186185	ATTATTTATATTAAG[G/T]GCCTCTCTGTAGGTT	100507650
rs569456259	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244876	TCTTCATTTAGTGTT[C/T]ATAACTGGTTGCTTG	100507650
rs569467525	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250660	TCTGAGACAAGTCTC[A/C]GTTAATTTAGAAAGT	100507650
rs569503372	in-del	-/A	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23216088	ATCTCTACTAAAAAT[-/A]AAAAAAAATTAGCTG	100507650
rs569527110	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23244083	AACTCTGTCTCAAAG[-/A]AAAAAAAAAAGTATA	100507650
rs569537188	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208670	GTGAGTCTGCAGTGC[A/G]AAGTGAAAGCAAGTT	100507650
rs569554253	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218121	TGCCTGTAATCCTAG[A/C]ACTTTGGGAGGCTGA	100507650
rs569569153	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196977	TCTAGACTGCAAACT[C/G]CATGAGTGCAGGGAC	100507650
rs569630817	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253523	TATCACCATCATTGG[C/T]TTGGGGGCGGGGAAA	100507650
rs569641359	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223395	GAGTCTTGCTCTGTC[A/G]CTCAGGCTGGAGTGC	100507650
rs569682333	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23268681	AAACCAAGGCACAGA[C/T]ACATGAGAGCACATG	100507650
rs569722837	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23227324	CTGTAATTATTTTAA[A/G]ACAAAAAGTTACAAT	100507650
rs569747379	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240938	GTGGTAATTATTAGT[A/G]GAATCATTTTACAAA	100507650
rs569773601	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23261654	ATATCTATGCTCTAC[C/G]AACTCTTAAATATAT	100507650
rs569777942	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218458	TAGAATTGATCAAGC[A/C]GAAGAAAGAATTAGT	100507650
rs569783061	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248305	GCTAGTTTTTGTGTT[G/T]TTTTTTTTTTAATAG	100507650
rs569791930	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196955	ATGATTAATGTCTAC[C/T]TCCCCATCTAGACTG	100507650
rs569811927	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23232942	AACGGGCCATGATGA[C/T]GATGGTGGTTTTGTG	100507650
rs569828955	snp	A/C	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23248560	AATTATCCTGCCTCC[A/C]CCTCCTGAGTAGCTG	100507650
rs569881224	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192961	GCCGGGCATGGTGGC[A/G]CATGCCTGTAATCCC	100507650
rs569897452	snp	A/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23254561	TATTACTTTTTTGTA[A/T]GTGTGTGCTTTTGGT	100507650
rs569932193	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201277	AGCTGGTTATAAAAC[A/C]ATCTTCTAAAGAGAA	100507650
rs570016381	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185312	GCACGAAACTCCATG[A/G]GAGGGAATGAGTCAT	100507650
rs570048418	snp	A/C			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214543	AAATTAATTTAATTT[A/C]AAAAAAGGACAACCA	100507650
rs570050557	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199255	AATCAATATATGTAA[A/G]AAGTACATTGGTTCA	100507650
rs570090423	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211854	CAGTCTCCCAAGTAG[C/T]GAGGACTACAGGCAC	100507650
rs570125468	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23222397	TAGAAGAAATGGATA[A/C]ATTTTTAGACATATA	100507650
rs570132204	snp	G/T	0.00676609	0.0577691	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196757	CCAAAGGGCTTTTTT[G/T]GTGTCCATGCTCTTC	100507650
rs570132475	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207638	AGATTTGTCAAAGGT[C/T]GGGGGCAACTCCACT	100507650
rs570141975	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23247137	ACGAGCAAAACTCCA[C/T]CTCAAAAAAAAAAAA	100507650
rs570240547	snp	A/C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192953	AAAAATTAGCCGGGC[A/C/G]TGGTGGCACATGCCT	100507650
rs570399464	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185268	AACAAACAACAACAA[A/C]AAAAACCAGACAAGG	100507650
rs570414331	snp	A/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23267436	TGTCTCTTGTAACAA[A/T]TTTTTTTTTTTTGGG	100507650
rs570417689	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23240189	TCACTGTATATGTAC[A/G]TATACTTCTTTACAA	100507650
rs570439995	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23229311	ATTTGTGTTGTTTCT[A/C]TCTTTTGGTTATTGT	100507650
rs570510420	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207802	TGTGCCCAAGGTGGT[A/C]GGGGTACAGCTTAGT	100507650
rs570516005	snp	A/G/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204851	TCTACCCATCCATGA[A/G/T]CATGGGGTATATTTT	100507650
rs570586022	snp	A/C	0	0	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213114	TCAGGAGATCGAGAC[A/C]ATCCTGGCTAACACA	100507650
rs570618325	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253940	CAAAAATTAAATTGC[A/G]TGCAAAAATAAATCT	100507650
rs570665930	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199107	AAAATTTGAGACAGG[C/T]CTCAGTTAATTGTTT	100507650
rs570721831	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208489	ACAGAGTGAGATCCT[A/G]TCTCTAAAAAAAATG	100507650
rs570735015	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200254	AGGAGGAATCTCAGA[C/T]AAGATTTTAAAGCTG	100507650
rs570745730	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23251973	GGTAACTCTCTGAAC[C/T]GCCTTGTTCAGGAGT	100507650
rs570782537	snp	C/G	0.000159681	0.00893391	intron-variant	RNF212B	GRCh38.p7	14:23258529	GGAGAGTATGTCAAA[C/G]GCTTGTTTTTCCCTA	100507650
rs570805201	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23191841	ATATAGAAGGCACTC[A/G]ACAAATACATACTTA	100507650
rs570844885	snp	C/T	0.00199481	0.0315187	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210733	AGTGAGCCAGGATCA[C/T]GCCATTGCCCTCCAG	100507650
rs570862856	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23216577	CTAAGTAAAAAAAAA[A/T]AAAAATAATAAGGCC	100507650
rs570874167	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23235392	TATTTATGGAATAGT[C/T]TGATTTGTAACCTGA	100507650
rs570883617	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23232580	GCCCAGCAGCCACCC[C/G]GTCCGGGAGGGAGTT	100507650
rs570918243	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23238681	AGTTCCAGGCTGCAG[C/T]GAGCCCTGATCTGCC	100507650
rs570981323	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23191001	CCCTTTCTCACATCA[C/T]GCACATCCCTCTGCA	100507650
rs571017406	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23261945	TGCACTCCAGCCTGG[A/G]TGACAGAGTGGGACT	100507650
rs571022247	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232786	TCTGGGAGGGAGGTG[A/G]GGGGGGGGTCAGCCT	100507650
rs571031707	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23228806	CAGTGGAACAGAATA[C/G]AGCATGCAGAAATGG	100507650
rs571035644	snp	A/C	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274751	CTCTACTAAAAATAT[A/C]AAAAAGTAGCCGGGT	100507650
rs571042583	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206695	AGCAAAATTTACATC[A/G]TAAGGTAGAGAGAGA	100507650
rs571068418	in-del	-/AAC	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23261977	GTCTCAAAACAAACA[-/AAC]AAAAAACAGAAAACA	100507650
rs571080078	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196216	CAGGTGCCGAAAAAT[G/T]TCTTTCTGATTGTAA	100507650
rs571093406	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232946	GGCCATGATGACGAT[A/G]GTGGTTTTGTGGAAT	100507650
rs571185084	snp	C/T	0.00517822	0.0506191	intron-variant	RNF212B	GRCh38.p7	14:23248592	GATTACGGGCATGCG[C/T]CACCACACCTGGCTA	100507650
rs571214452	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189127	ACCACAATCTTGTAG[A/T]TAACTGACCTTTCCA	100507650
rs571284462	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214232	GGCATGGCGGCTCAA[A/G]CCTGTAATCCCAGCA	100507650
rs571304479	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23234611	TTAAAATTTATTAAC[A/G]TACTTGGTTCTATTT	100507650
rs571348416	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231842	AGAGGGGGTTTCGCT[A/G]TGTTGGCCGGGCTGG	100507650
rs571384003	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203200	GCCTGTGTATCTTTA[C/T]AGCTTAGCTTCCACA	100507650
rs571423955	in-del	-/AAA	0.177503	0.239258	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213695	CTGTGTGCTCTACCT[-/AAA]CAGGGTGACTGCATG	100507650
rs571461500	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261969	TGGGACTCTGTCTCA[A/G]AACAAACAAAAAAAC	100507650
rs571488548	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225564	CCAGGCACAGAAAGA[C/T]AAACATTTCATGTTC	100507650
rs571504837	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23272192	GGAGGCCGAGGCGGG[C/T]GGATTATGAGGTCAG	100507650
rs571549626	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269822	TATTTTTACCTTTAC[A/C]TGTCCTTTTCTCTGC	100507650
rs571619605	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223500	AGCTGGACTACAGGC[A/G]CCCGCCATCAAGCCC	100507650
rs571624407	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23262811	ATGTGATCTTCCTAA[C/T]TTTATGTGTAATATG	100507650
rs571637413	snp	C/T	0.00358779	0.0422022	intron-variant	RNF212B	GRCh38.p7	14:23193927	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	100507650
rs571641897	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23249205	TCAGGTCAAGATTTG[A/G]TCTCATCAATAGACC	100507650
rs571678487	in-del	-/AACA			intron-variant	RNF212B	GRCh38.p7	14:23272427	CCATCTCAAAAAAAC[-/AACA]AACAAACAAACAAAC	100507650
rs571687492	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230791	TTTTGAGTTAATTTT[G/T]GTATATGGTGTAAGG	100507650
rs571701231	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200473	TGGGATTACAGGTGC[A/G]TGCCACTGTGTCTGG	100507650
rs571712124	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208011	AAGGAGGCAATCAGA[C/T]ATGCATCTATATCAG	100507650
rs571786562	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200585	CCCACCTCGGCCTCC[C/T]AAAGTGCTGGGATTA	100507650
rs571823618	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223651	TGAGCCACCGCGCCC[A/G]GCCAAGCCTTTCTTT	100507650
rs571982316	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223792	ATTGGAAAGGAAAAG[C/G]TCAAATTATCCTTGT	100507650
rs572002792	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23189802	AACAGAGTGAGTTCT[C/T]ATCTGAAAATATGTG	100507650
rs572028385	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193405	TTCAGGAATAAGGTA[A/C]CACAACTAGAGACAG	100507650
rs572067905	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184228	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCG	100507650
rs572069090	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234227	AAAAGCTCTTTGTAT[A/G]TTAAAGCTATTAGCC	100507650
rs572098712	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23247793	GGGTATATACCTACG[A/G]GTGGAATTTCTGGGT	100507650
rs572109712	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274679	TTGGGAGGCCAAGGT[G/T]GGCGGATCATGAGGT	100507650
rs572205909	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184909	ATAAAGTTATTTTTA[A/G]CCTTATTAAATATAT	100507650
rs572219756	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218962	AGGAGAAAAGAAACA[A/C]ATAACAAAATAGAGC	100507650
rs572223127	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23194123	CTGGGTTTACAGGCA[C/T]GAGCCACCATTCCTG	100507650
rs572226173	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23261620	CTGGATATATACCAC[C/T]GGTCCTTTCTAATTA	100507650
rs572235010	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269326	AACAAAAAAACAAAA[A/C]TCTGCCAGCAGTCCT	100507650
rs572287144	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23231002	CTTATGCTAGAAACA[C/G]ACTGTTTTGATTACA	100507650
rs572346541	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270069	GCCCCCCAAAGAGCA[C/T]TGTCTCTAGTTGGCT	100507650
rs572429407	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23267074	TCCAGGCTTAAGCGA[C/T]AGTCCCACTTCAGCC	100507650
rs572508840	snp	G/T	0.00199481	0.0315187	intron-variant	RNF212B	GRCh38.p7	14:23271501	TGCCTTTTTTTGTTT[G/T]TTTTTTTTAATGGCT	100507650
rs572536733	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23227831	CTCAAACTCCTGGAC[C/T]CAGGTGATTCACCCA	100507650
rs572538363	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23217505	CCCAGCACAGTCCCA[A/G]TGGTGGTTGCCACAT	100507650
rs572551581	snp	A/G	0.000399281	0.0141238	synonymous-codon, intron-variant, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23260667	CCTATAGGAATCTCC[A/G]AGTCGGTACCAAGGA	100507650
rs572586315	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23228954	TGTTGTACAATCATC[A/G]TCTCTATTTCCATAA	100507650
rs572623463	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23253186	TCTTAAATATAACCA[C/T]ATCATGCTAAAATAA	100507650
rs572667338	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23223132	TGCAAGGATGGTTCA[C/G]ATATGCAAATCAATA	100507650
rs572676909	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23249438	GTAGTCCAGCTACTC[A/G]GGAGGCTGAGGTGGG	100507650
rs572708102	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189235	TGGAGAAAATGGGAA[C/T]AGGCAGAAGAGAACT	100507650
rs572744463	snp	G/T	0.00037154	0.0136247	synonymous-codon, intron-variant, missense, nc-transcript-variant	RNF212B	GRCh38.p7	14:23264652	GCAGGGAAGGAGAAC[G/T]CCCAGAGACTCTTAT	100507650
rs572814806	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23188766	TGAACCACTGTGCTG[C/G]GCCTCAGGTTTTTAA	100507650
rs572893540	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196325	TATCATGCCAAAATG[C/T]ATGGCCCAACCTCCA	100507650
rs572949487	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250266	GGTGGATCACTTGAG[A/G]TCAGGGGTTCAAGAT	100507650
rs572974217	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242286	TTTGTCTCCGTGAAG[C/T]ATATGCCATGTGATG	100507650
rs573012670	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23225790	ATTTAATCATACATT[A/T]AAAAATAACTAAAAG	100507650
rs573038845	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210437	TGGAGTTTAGTTAAT[C/T]ATAATGTGCCAATGT	100507650
rs573091187	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23242549	ATAGAATAAAAAAGA[A/G]TAACTTAAAGTTAAG	100507650
rs573128988	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23240976	ACTGGCTCAGAGAGG[A/G]TAAGTGATTTGACCA	100507650
rs573146279	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23255303	TCAAAGCCAGTTAAT[A/G]TCTTTAAACTAAATT	100507650
rs573160464	snp	A/G	0.00398564	0.0444627	intron-variant	RNF212B	GRCh38.p7	14:23220401	GCTGGGTCTGGTGGT[A/G]CACACCTGTAGTTCC	100507650
rs573269863	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255839	ATTTTTTAAAGTACT[A/G]TACTGAGGTACATTA	100507650
rs573270972	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208972	ATCGTGTTAGCCGGG[A/G]TGGTCTCGATCTCCT	100507650
rs573332433	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213826	ACTCAAAATGCTTAG[C/T]ATATAATCAAAAAGC	100507650
rs573336191	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23231424	ACATGCAAAACACAC[C/G]CACATATGCACATGC	100507650
rs573377801	snp	A/G	0.00636936	0.0560724	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209157	AGATAACTTCCTGAC[A/G]TTGCCATGGCATTTG	100507650
rs573469838	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205945	TAAGTATGAAATTTG[C/T]TTGATTAATAATGCA	100507650
rs573480585	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23248937	CAGGCCATACAATTT[C/T]CGATGCTGCTACCCA	100507650
rs573496725	snp	A/G	0.00716266	0.059414	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201980	TGGAGGCCGGGCACA[A/G]TAGCTCATGCCTGTA	100507650
rs573503327	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236241	AACATTTTGGCCAGG[C/T]GCGGTGGCTCACACC	100507650
rs573535401	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236160	CAAAAATGTAAAAAC[A/G]ATGCCACTCTTCTCA	100507650
rs573558529	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195588	TTCATGCACTCATTT[C/T]GTGTGCTCAGTATCT	100507650
rs573589901	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242492	GGTAGGCATAACTGG[A/G]GACTTTCTTACAGTG	100507650
rs573621021	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23235651	CCCAAGACTCAAATA[C/T]TTACCTGATGAGATA	100507650
rs573708001	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210516	GGCGTGGTGGCTCAC[A/G]CCTATAATCCCAGAA	100507650
rs573726423	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23263765	CCCCAAAAAAAACGA[A/G]TGTTCTGTGTGCTAA	100507650
rs573729965	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23225043	ATGCAAATTGAAACT[A/G]CAGTGATCAGATTAA	100507650
rs573762696	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23272270	AAAAAAGTACAAAAA[A/G]TTAGCCGGGCATGGT	100507650
rs573781448	snp	A/C	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23254299	CTCAAAAACAAAACA[A/C]AACAAAACAAAACAA	100507650
rs573792335	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23224078	CATTGATGAAAGAAA[A/T]TGAGGAGAACACACA	100507650
rs573794358	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23231884	TAACCGTGAGTGATC[C/T]GCCAGCCTCGGCCTC	100507650
rs573856804	snp	C/T	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23248630	TATTTTTAATAGAGA[C/T]GGGGTTTCACCGTGT	100507650
rs573882829	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23220286	CCTGTAATTTCAGCA[C/T]TTTGGGAGGTCGAGG	100507650
rs573944598	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23218264	TCCCAGCTACTCAGG[A/G]GGCTGAGACAGGAGA	100507650
rs573951551	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23261578	CAATATTAAGTGCCT[A/G]CTGTTTATCAGGTAC	100507650
rs573971991	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23223535	AATTTTTTTGTATTT[G/T]TAGTAGAGACGGGGT	100507650
rs573986952	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23269150	TCTCTACTAAAAATA[A/G]AAAATTAGCCGGGAG	100507650
rs574010680	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210559	GAGGCGGGTGGATCA[C/T]GAGGTCAGGAGTTTG	100507650
rs574054857	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23223453	CTCCGCCTCACGGGT[A/T]CACGCCATTCTTCTG	100507650
rs574091415	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23222029	ATAAGTGTCTACATC[A/G]AAAAGGAAGAAGAAC	100507650
rs574108935	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23218886	AAGAAGAGTACCTCC[A/G]GGCATTTAATAATCA	100507650
rs574109391	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23186507	GGCACCTGCCACCAT[C/G]CCTGGCTAATTTTTG	100507650
rs574113831	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241367	TGATGGAAGGCTCTA[C/T]ACACTGGGCTAAAGA	100507650
rs574119092	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209230	CCAGAGGTCACTCTC[A/G]TAGCCATTTTGGTTT	100507650
rs574146224	snp	C/T	0.00398564	0.0444627	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213261	GAGCTTGCAGTGAGC[C/T]GAGATCGCACCACTG	100507650
rs574172553	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197215	TCACTGATGTTATCA[G/T]CCAGAAAGGGTGAGA	100507650
rs574230075	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23241783	TGGCAACGTTACGGA[C/T]TGGGAAAAAGAAAAA	100507650
rs574231991	snp	A/C/G	0.0138799	0.0821421	intron-variant	RNF212B	GRCh38.p7	14:23241381	ATACACTGGGCTAAA[A/C/G]AGCCTGAACTTCATC	100507650
rs574251322	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201865	GAGCCAATTCCACTT[A/G]CTTTTCCAAATTTTG	100507650
rs574270116	snp	A/G	0.0115144	0.0749975	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208815	CCAGGCTGGAGTGCA[A/G]TGGCGCGATCTCAGG	100507650
rs574292042	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200976	TCAATTACAGAGAAA[A/C]AAATATGCTCCAAAT	100507650
rs574298590	snp	A/G	0.00716266	0.059414	intron-variant	RNF212B	GRCh38.p7	14:23241939	TACAAAAAATTAGCC[A/G]GGCATGGTGGCGGGC	100507650
rs574304373	snp	G/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23258113	GGAGGCTGAGGTGGG[G/T]AGATCACCTGAGGTC	100507650
rs574321474	in-del	-/CAAA	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205959	GCTTGATTAATAATG[-/CAAA]CAAAGTGTATGCTGG	100507650
rs574340208	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221401	AAGAAGAGACAAAGT[C/G]ATTCTATAATGATAA	100507650
rs574426341	snp	A/G	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208965	GGGTTTCATCGTGTT[A/G]GCCGGGATGGTCTCG	100507650
rs574474461	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23257856	CTGTAGGTGTCTTTA[C/G]GGAAAATAAATTGGT	100507650
rs574494545	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209676	TGAGGGTAGGCTGGA[C/T]TGAGGGACTCTCTTT	100507650
rs574570783	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203881	TGATCACCGTATCCA[C/T]GCCAACATCTACAGT	100507650
rs574664327	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23251689	GGTGTGGTGGCGGGC[A/G]CCTGTAATCCCAGCT	100507650
rs574666691	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232279	GGGATGTGAGGAGCG[C/T]CTCTGCCCGGCCGCA	100507650
rs574687667	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205112	TTTTAGGACTAAACA[C/T]TTACTATAAAAGATT	100507650
rs574737189	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23243552	ATATAAAAAATTAGC[C/T]AGGCGTGGTGGTGCG	100507650
rs574788428	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23267521	GCAACCTCCTCCTCC[A/T]GGCTTCAAGTGATTT	100507650
rs574808555	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226575	GGCGGAGCTTGCAGT[A/G]AGCCGAGATCGCGCC	100507650
rs574826601	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205924	ACCTTACATTATTTG[G/T]CAGGGTAAGTATGAA	100507650
rs574854306	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196570	TCAGCCTCCTGAGTA[C/G]CTAGGACTACAGGGC	100507650
rs574859686	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244170	AATTGGACATATAAT[A/G]TACATCTAGAAGAGT	100507650
rs574860865	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23191364	AAAAAAAAAAAAAAA[-/G]AAAAGCAAGAAAGTC	100507650
rs574945854	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23218873	CAGATTTAACCCAAA[C/G]AAGAGTACCTCCGGG	100507650
rs575022593	snp	A/G	0.00279162	0.0372561	intron-variant	RNF212B	GRCh38.p7	14:23267870	AAGTGAGTATCTTGT[A/G]GACTGTGCATAGTTG	100507650
rs575076282	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190484	ACTTATCTTTTTCTC[A/G]TATATCCTACATTTG	100507650
rs575105903	in-del	-/G	0.209388	0.246679	intron-variant	RNF212B	GRCh38.p7	14:23232785	GTCTGGGAGGGAGGT[-/G]GGGGGGGGGTCAGCC	100507650
rs575123677	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23226499	AGCCGGACATGGCGG[A/C]GTGCGCCTGTAGTCC	100507650
rs575138194	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23273090	TTACAAAAGGCTAGT[A/G]CTTCAGGAAGATGTT	100507650
rs575166027	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273885	AAACAACCTGGCTGG[C/T]GATAGATGCTGAACT	100507650
rs575248757	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214445	GTTGCGGTGAGCCCA[A/G]ATTGCGCCAATGTAC	100507650
rs575310533	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23245165	CTTTTGAAAATACCC[A/C]TTTTCTAAACCTCAA	100507650
rs575339856	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23189694	CATGCCTGTAGCACC[A/G]GCAACTCAGGAGGCT	100507650
rs575347255	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266053	GCCATCTCAGCTCAC[C/T]GCCACCTTCGCCTCC	100507650
rs575354828	snp	A/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23244545	TCCTTGATGATACAA[A/T]TTTCAATCAGTTAAC	100507650
rs575388711	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23221701	CATTCTTCTTTTTAG[C/T]GCATGGGTAATTCTT	100507650
rs575408991	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23230165	GTGGAAAAAGGAAGA[C/G]AGAGAGAGTTGTAGT	100507650
rs575413346	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23242026	GGCAGAGCTTGCAGT[C/G]AGCCAAGATCGTGCC	100507650
rs575440750	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250956	GTATCTCAGTGAGCA[A/G]AAGGGTGACTTTGAA	100507650
rs575464623	in-del	-/A	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205175	TCTTACTACACACAC[-/A]AAAAAATCTCTTTAT	100507650
rs575468974	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23245075	AGATTATTCTATAGC[C/T]TCATGGAATTCCTAT	100507650
rs575482715	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209086	TTATGGTTATGTATT[G/T]ATGATATGCTAAACA	100507650
rs575515408	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23261075	TCTACCTTACTGCTG[C/T]GTCCGGTTTCCATTG	100507650
rs575520373	snp	A/G	0.00119737	0.0244387	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210509	TGGGGTGGGCGTGGT[A/G]GCTCACGCCTATAAT	100507650
rs575520878	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23221112	ACACTTCAGGCCAGG[C/T]GCAGTGGCTCACGCC	100507650
rs575535461	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23247305	GTATGCAATTCAGTG[C/G]TTTTTAATACATCCA	100507650
rs575550079	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232136	GAGCCCCTCTGCCCG[A/G]CTGCCCACTCTGGGA	100507650
rs575633920	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212174	ATTGTAGCCAGCCTT[A/G]TACATAATGGTGAAA	100507650
rs575637168	snp	A/C	0.00159617	0.0282053	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209615	TCCAAATTTTAAATA[A/C]TATATGTAGATACTT	100507650
rs575668181	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23250152	CATATACTTTCATAC[C/T]TTTATACCTGAAATG	100507650
rs575678680	snp	C/G	0.000798403	0.0199641	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202841	GGCGACAGAGCGAGA[C/G]CCTGTCTCAAAAAAA	100507650
rs575748497	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198370	ATAATCAAATTTCTT[A/C]AAATATCAAAAAAGG	100507650
rs575752389	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23255912	ATAGGCTAAACATTT[G/T]TACCCTGGCATCAGG	100507650
rs575772045	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203335	TTGATGGGCATTTGG[A/G]TTGGTTCCACGATTT	100507650
rs575781765	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23243475	TCAAGGCGGGTGGAT[A/C]GCCTGAGCTCAGGAA	100507650
rs575822005	in-del	-/C	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23187032	AGGACTTCACCTGGG[-/C]CCCCCCAACATTTGT	100507650
rs575868102	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196479	GGGGCCTGCTCTGTC[A/G]CACGGGCTGGAGGGC	100507650
rs575872955	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23233471	TGGCTCATGCCTATA[A/G]TCCCAGTACTTTAGG	100507650
rs575887034	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23230420	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	100507650
rs575932901	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195803	AATTTCATCATGTTT[A/G]ATTTCGTTTAACCTT	100507650
rs576079701	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23239657	GGAGTCTGGCTCTGT[C/T]GCCTAGGCTGGAGTG	100507650
rs576095600	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207129	GCTGCTATTTCAGAA[G/T]TACAGCCAACAACAA	100507650
rs576118480	snp	C/G	0.00557542	0.0525036	intron-variant	RNF212B	GRCh38.p7	14:23191101	GCTCACTCCTGTAAT[C/G]CCAGCGCTTTGGGAG	100507650
rs576210543	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200200	ATAATTATTTTTTAC[A/T]TAGGCTTTTAAATGG	100507650
rs576254611	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23268192	AAGACAACCTTGAAA[A/G]TGGGGTCTTCCAGGG	100507650
rs576269316	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23265986	GTTTGTTCATTTGTG[-/T]TTTTTTTTGAGATGG	100507650
rs576294279	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23217314	GGAAGAACTTTATAT[C/T]GTGGTGTGAGTGCCA	100507650
rs576294305	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211548	CAAAATCATACAAAG[A/G]TCGTACCAGAAAACT	100507650
rs576300264	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23191524	GTTGGTTTTTCTAGG[A/G]GGTAATGATATTACA	100507650
rs576330064	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192618	TGCAGCACACCAACA[A/T]GGCACATGTATACAT	100507650
rs576382459	snp	C/T	0.00279162	0.0372561	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197968	CACAAAGTACATTCT[C/T]AAGGGCGGGGGAGAT	100507650
rs576393125	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23185858	TAATTCCAGCACTTT[C/G]GGAGGCCGAAGCAGG	100507650
rs576412946	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23228172	TGGAGGTGGAGATTG[C/T]GGTGAGCTGAGATCG	100507650
rs576422197	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218194	TAACACGGTGAAACC[C/T]CGTCTCTACTAAAAA	100507650
rs576484092	snp	C/T	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23232609	TTGGGGGGTCAGCCC[C/T]CGCCCGGCCAGCCTC	100507650
rs576568503	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23266207	CAGGTGATCTGCCCG[C/T]CTCAGCCTCCCAAAG	100507650
rs576628945	in-del	-/ATTTTTGTTGATGTCACTCCTAGCTA	0.0240643	0.107019	intron-variant	RNF212B	GRCh38.p7	14:23268567	GGTCTTTGCTCTGCC[-/ATTTTTGTTGATGTCACTCCTAGCTA]ATTTTTGTTGATGTC	100507650
rs576645010	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23256805	AATCCACCCACTTCA[A/G]CCTTTCAGGTAGTTG	100507650
rs576684381	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23259152	GCTATGATCACACCA[C/T]GACACTCCAGCGTGG	100507650
rs576794208	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23252379	AAAATCAGCCCATTA[A/G]AAAAAAGTTTATTAT	100507650
rs576796387	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260055	CATCATGGCACACAC[A/G]GAAATTGATATTTGT	100507650
rs576843296	in-del	-/GTGCAATGGCGCGATCTCAG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208810	GTCGCCCAGGCTGGA[-/GTGCAATGGCGCGATCTCAG]GTCACTGCAAGCTCT	100507650
rs576845552	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203986	CTGATCACTAGTGAT[A/G]CTGAGCATACGTTTG	100507650
rs576860619	in-del	-/AG			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194867	TGTGCATTAAAAAAT[-/AG]AGACTATACATTATT	100507650
rs576863291	snp	A/G	0.00597247	0.0543191	intron-variant	RNF212B	GRCh38.p7	14:23255050	CCAAGAAATCAGGAG[A/G]GAGAGAGGTAATAGC	100507650
rs576878811	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23271108	CAACAAAAGGTAAAG[A/G]GCATGGTAACAAGGA	100507650
rs576891664	snp	A/G			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236978	TTTTTTTTTTTTTTT[A/G]TTTGAGGCAGTGTCT	100507650
rs576910284	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211448	AAGAAAAAAATAATG[C/T]CAATTCTACACAAAT	100507650
rs576986495	snp	C/T	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23258951	AGCACTTTGGGTGAC[C/T]GAAGCAGAAGATCAC	100507650
rs576998284	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23246938	CTGAGGTCCGGGGTT[C/T]GAGACCAGCCTGACC	100507650
rs577071220	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199503	GATTTGGGGGCCCCA[A/G]GCTTTAATTTCCTTT	100507650
rs577082638	snp	A/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23233358	CACTATTGTCCTATG[A/T]CCCTGCCAAATGCCC	100507650
rs577096709	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23221919	ATATTAAGAAGGAAA[C/T]TGAAAAGTGCCTTGA	100507650
rs577177514	snp	C/G	0.00119737	0.0244387	intron-variant	RNF212B	GRCh38.p7	14:23194298	ATAAAATAATTAAAA[C/G]AACACTCAAGAAGAT	100507650
rs577201643	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23192478	ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA	100507650
rs577226500	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23232533	TCTGCCCAGCAGCCA[C/T]CCCTCTGGGAGGGAG	100507650
rs577302004	snp	A/C	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23245038	AACTTTGGTTTTTTT[A/C]CTTCTACTCCCCATT	100507650
rs577314182	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194916	TATTTAAAAACATTT[C/T]GATTTACTGGGTCAC	100507650
rs577331928	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23234497	TTATCCTGGTAAACA[C/G]TATGAGAAACAGACT	100507650
rs577339140	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23244255	GGTACATCTTTTGTC[A/G]TGTTAGTCAGTATTT	100507650
rs577361109	snp	C/T	0.00755907	0.0610114	intron-variant	RNF212B	GRCh38.p7	14:23227562	TGAATATACATTAAA[C/T]GTCAATATACATTGA	100507650
rs577372320	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23187366	ACTCCCCCCTTTTTT[A/G]GAGACAAGGTCTCAC	100507650
rs577396631	snp	A/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23190585	CTTACCATTTCCACT[A/G]CTACCACCCTGGTTC	100507650
rs577485168	snp	A/C	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23265369	GTTTTAAACATAAAA[A/C]TATTCCAGTGAAGGA	100507650
rs577502562	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23228078	TCTACTAAAAATACA[A/G]AATTAGCCAGGCGTG	100507650
rs577548730	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23219473	TCTCCTTCTTCTCCT[C/T]CTAGTTTTTTTTTTT	100507650
rs577575744	in-del	-/TTTTG	0.00159617	0.0282053	intron-variant	RNF212B	GRCh38.p7	14:23241714	AGGTGTAAGCCATTT[-/TTTTG]TTTTGTTTTGTTTTG	100507650
rs577588629	snp	A/C	0.000399281	0.0141238	intron-variant, missense	RNF212B	GRCh38.p7	14:23268060	TATCTCCTTAGGCAG[A/C]CAAACAAGTGCTTCT	100507650
rs577685321	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23230544	CTGTAGTCCCAGCTA[C/T]TCGGGAAGCTGAGGC	100507650
rs577693365	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23234949	CTGGGTACGGTGGCT[C/T]ATACCTGTAATCCCA	100507650
rs577698830	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260844	AAGTGCCGAAGTAAA[A/C]TCTTAATTGTAATGC	100507650
rs577705379	snp	C/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23241849	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	100507650
rs577736738	snp	C/T	0.0023933	0.0345097	intron-variant	RNF212B	GRCh38.p7	14:23271220	GAGGCAGGTGGATAA[C/T]CTGAGGTCAGGAGTT	100507650
rs577746269	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218636	CAGAGTCAGAGGAGA[C/T]GAAAGAAAATAAAAA	100507650
rs577764992	snp	A/G	0.000798403	0.0199641	intron-variant	RNF212B	GRCh38.p7	14:23224014	ATAAAATTAATTACC[A/G]AGGAATTAACCAAAG	100507650
rs577851462	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273516	GAATGGTGGAATGGG[C/T]GAACAACACTATCAC	100507650
rs577897284	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229902	TTTTAGCTTGATATG[A/G]TAAGATGGTTATGAG	100507650
rs577938331	snp	A/C	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23185679	GGGATCAAATACGTT[A/C]TTGGAATACAGCGGT	100507650
rs578068870	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23247678	CATTCATTAGTCAAT[A/G]GACATTTGGGTTGTT	100507650
rs578079243	snp	G/T	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23248002	AAGTTCAACATCAAG[G/T]CACTAACAGATTCAG	100507650
rs578092543	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B	GRCh38.p7	14:23193223	ATGATTTTCAACTCA[C/G]AAAATTATACATAGC	100507650
rs578111001	snp	A/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184749	ACTAGCTTATTACCA[A/T]ATCGAAATGATGCCT	100507650
rs578121725	snp	C/T	0.00318978	0.0398085	intron-variant	RNF212B	GRCh38.p7	14:23218228	AAAAAATTAGCCGGG[C/T]GTGGTGGCACACACC	100507650
rs578254688	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209584	TGGAAACAAATCTTT[A/G]CAGAATACTTTGACT	100507650
rs578262463	snp	C/G	0.000399281	0.0141238	intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208274	CACTTGTAATTCCAG[C/G]ACATTGGACGAGAAG	100507650
rs745328731	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23250080	AAGTTATTACGTAAG[G/T]TTATTTATTACCTAA	100507650
rs745413955	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23190203	AGCTGTGTGATGTCA[A/T]CCAGTCCCATGGCTT	100507650
rs745508814	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23251521	CAGTTTATTATAAAA[G/T]ATACAACATAGGGGC	100507650
rs745560318	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23191631	TTGTTTCAAATAACA[C/T]AGGAGGAAGAATAGA	100507650
rs745599994	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23271815	ACAAGCTGTAAAAAA[A/T]ATAAATAAAACAATT	100507650
rs745604555	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23238252	GGGCATATAGAACGG[A/G]GCCTTTTCAGTGGTT	100507650
rs745612104	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23257193	ATAAATCAAAATTAT[C/T]TTTCATAGAGACAGG	100507650
rs745658963	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23193905	GGAGTGCAGTGGCGC[A/G]ATCTTGGCTCACTGC	100507650
rs745736338	snp	A/G	0.000124324	0.00788331	missense, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23259933	CTGAAGAAATTTCTA[A/G]CCATTCTAAAGGTGA	100507650
rs745773615	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23245029	AGTTGTAAAAACTTT[G/T]GTTTTTTTCCTTCTA	100507650
rs745829525	in-del	-/TGCATTGGGAG			intron-variant	RNF212B	GRCh38.p7	14:23248835	ATCTCTTAATACTAT[-/TGCATTGGGAG]TTGAGTGTCAACAAA	100507650
rs745843406	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198901	CCTTGGGTAGTGGAT[A/T]AGAGTTGGTTAGCTA	100507650
rs745852342	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213434	AGTCAATTTTTCCCA[A/G]TTTGATCTATAGATT	100507650
rs745883644	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23247555	AAGTATAATGCTCTC[A/C]AGTTTCATCCATGTT	100507650
rs745955804	in-del	-/AAAT			intron-variant	RNF212B	GRCh38.p7	14:23271814	AACAAGCTGTAAAAA[-/AAAT]AAATAAAACAATTCA	100507650
rs745986394	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218478	AAAGAATTAGTGAGT[C/T]TGAAGACAAGCTATT	100507650
rs746151873	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23239825	GGTTTCACCATGTTG[G/T]CCAGGCTGGTCTTAA	100507650
rs746197801	in-del	-/AAAACAAAAACC			intron-variant	RNF212B	GRCh38.p7	14:23220229	ACAAAAACAAAAACA[-/AAAACAAAAACC]ATACAACAAGGCCAG	100507650
rs746264374	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195383	AGCTATCAGAGGAAC[C/T]AAATGGAATTATAAG	100507650
rs746300487	snp	A/G	0.00024667	0.0111029	missense, utr-variant-3-prime, synonymous-codon, nc-transcript-variant	RNF212B	GRCh38.p7	14:23272839	CTCTCTACCAACAAC[A/G]GAGGCATATGGGATT	100507650
rs746443220	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23224834	CCACAGAATGAGAGA[A/C]TATATTTGCAAACTT	100507650
rs746535809	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202042	GACTGCTTGAGGTCC[A/G]GAGTTCGAGACCAGC	100507650
rs746638620	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23248933	TTTGCAGGCCATACA[A/G]TTTCCGATGCTGCTA	100507650
rs746680521	in-del	-/CAA			intron-variant	RNF212B	GRCh38.p7	14:23223054	AGTGAAACTCCGTCT[-/CAA]AAAAAAAAAAAAAAA	100507650
rs746712663	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23188780	GGGCCTCAGGTTTTT[A/C]AAGATGTAGATGACA	100507650
rs746726188	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23250062	CCTCTCATGTACAAA[C/T]ACAAGTTATTACGTA	100507650
rs746786126	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23190028	AATCTAGCAATCATT[C/T]CTCAGTCTTTATCTT	100507650
rs746799634	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23191055	TTCTCTGACCACCCA[A/G]TAGAAAGTCCATCGC	100507650
rs746806368	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211738	ATTAGTATTATTATT[A/T]TTGAGACAGAGTCTC	100507650
rs746891962	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23249645	TTCTGAAACAGTGTA[C/G]TTGAATTCTTCATCA	100507650
rs746919297	snp	G/T			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270232	CTGGCTTCTCAAAAG[G/T]CCCTATATTGAAAAT	100507650
rs747009422	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23222373	TATATGTCAATAAAT[C/T]GGAAAATCTAGAAGA	100507650
rs747031387	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197089	TGAATGAATGTATAT[A/T]GGACATGTATGTGGT	100507650
rs747042231	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23244577	TTTTATTGACCCAGA[A/G]TCTGTGATAGGCTGT	100507650
rs747081396	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23246448	ATCTAATGACCAACT[C/T]GGCCTGCTAACTTAT	100507650
rs747100704	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198738	TAAGTCTGTTTCTCA[C/T]GGTATATGGGTTAAT	100507650
rs747101402	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211966	GTCCTGACCTCAAGT[C/T]ATCTGCCCTCCTCAG	100507650
rs747119395	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23217574	GAGCACACAGAGAGA[C/G]AGCTTCCATTTTGGG	100507650
rs747163604	snp	C/T	0.000579676	0.0170148	intron-variant	RNF212B	GRCh38.p7	14:23243318	GATAATGTAAGTTTT[C/T]CTCCCCCTGCCACAA	100507650
rs747210917	in-del	-/GG	0.000309262	0.0124312	intron-variant	RNF212B	GRCh38.p7	14:23262878	TGGCCAGGCAAGGCA[-/GG]GGCATACCATTGATG	100507650
rs747212579	snp	A/G			synonymous-codon, intron-variant, missense, nc-transcript-variant	RNF212B	GRCh38.p7	14:23264189	TCGGTCCTCCTCAGC[A/G]GAATCTATTCCTTAT	100507650
rs747257259	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23189515	CTCCCATTGAAAAAC[-/A]AAACAGGCCGGACTG	100507650
rs747270326	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23217351	CTGCACTAGGACATC[A/G]GCTAAACTGCTAAGA	100507650
rs747312083	in-del	-/TCCCC			intron-variant	RNF212B	GRCh38.p7	14:23226743	TCTCGGCTAGTCCCC[-/TCCCC]TCCCCTCCCCTCCCC	100507650
rs747326916	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23234297	TTGTGCTTTACTTTT[A/C]GTGTGTGTGTGTGTG	100507650
rs747378521	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206795	TATACTCTGTCTTAA[A/T]AACCCAAGAGTAGCC	100507650
rs747519714	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23272289	GCCGGGCATGGTGGC[A/G]GGCGCCTGTAGTCCC	100507650
rs747521329	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273421	TGTTGGAGACACTGA[-/T]TTTTCAGCTTAGTAT	100507650
rs747531699	in-del	-/CTGT			intron-variant	RNF212B	GRCh38.p7	14:23232334	CTCTGCCCGGCTGCC[-/CTGT]CTGTCTGAGAAGTGA	100507650
rs747563986	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273252	TCACTGTTTCATTTC[C/T]GGATTTCATTTTTAG	100507650
rs747582246	in-del	-/CGAGAG			intron-variant	RNF212B	GRCh38.p7	14:23228213	CTCCAGCCTGGGTGA[-/CGAGAG]CGAAACTCTGTCTAA	100507650
rs747631779	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237501	AATATCACACTGTTC[C/T]TTGTCCGCATCATTT	100507650
rs747774375	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259863	ATTTGCTGGAGCTGA[C/T]TGTTTCCATCTTTTG	100507650
rs747806739	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23225873	AAAGGATAAAAGCAC[C/G]AGGGGATCGATACCC	100507650
rs747883877	in-del	-/GA			intron-variant	RNF212B	GRCh38.p7	14:23255048	TCCAAGAAATCAGGA[-/GA]GAGAGAGAGGTAATA	100507650
rs747887116	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23248737	GAGCCATCACGCCCG[A/G]CCCCCAAGCCTCTTT	100507650
rs747889397	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23247860	GCCAGACTGTTTTCC[C/G]AAGTGGCTGTACCAT	100507650
rs747903650	snp	C/T	0.00023092	0.0107428	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270593	ACTGTTCCATTCTAT[C/T]CTTCAGCTCAGAGGG	100507650
rs747915011	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23235065	AAGAATACAAAAATT[A/G]ACCAGGCGTGGTGGC	100507650
rs747967515	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201900	CAATCTATAAAGTTT[A/G]TTCTTGAGTATAAAA	100507650
rs747992294	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23247813	AATTTCTGGGTCAAA[C/T]GGTAACTCTATATTT	100507650
rs748027981	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23267301	TATTGTCAAATTGTC[A/T]TATTTTCTCTTCAAT	100507650
rs748072703	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23220654	CACGGTGAAATCCCA[A/T]CTTTACTAAAAATAC	100507650
rs748106102	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23219571	CTGCCACCTGGGTTC[A/T]AGTGATTCTTGTGCC	100507650
rs748133082	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23268494	GATTTCTGAAAAAGT[A/T]GATTCTGACCATTAT	100507650
rs748214354	in-del	-/AG			intron-variant	RNF212B	GRCh38.p7	14:23268297	CCTCTAGTGACTGCC[-/AG]ACTGTTGGGTTTCAT	100507650
rs748223084	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23254763	AACGTCTTGTCTTAT[C/T]ATAGTAAACCTACTA	100507650
rs748227569	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210442	TTTAGTTAATTATAA[C/T]GTGCCAATGTTGGTT	100507650
rs748262031	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196282	ATTATTCTTTCTGCT[C/G]TTTCTCCAGCCTGCC	100507650
rs748299956	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23256663	AAGCATGAGCCACCA[C/T]GCCTGGCCTCCTCTA	100507650
rs748317625	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197241	TGAGAAAAATATAAC[A/G]AGAGGCCAGGCACTG	100507650
rs748349673	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23256953	AGGTCAGGAGTTCGA[C/G]ACCAGTCTGACCAAC	100507650
rs748416206	in-del	-/GCAGTGGTGG			intron-variant	RNF212B	GRCh38.p7	14:23217248	GTGGTGGCAGTGGTG[-/GCAGTGGTGG]GGGGGGGGCTCCTCT	100507650
rs748445322	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244512	ATGGAGGGAAATTGA[C/T]TGCTTTCTTTGCTTT	100507650
rs748458735	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23262866	ATGTACAACAAATTG[A/G]CCAGGCAAGGCAGGC	100507650
rs748459280	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184377	CCTGTAGTCTTAGCT[A/G]CTCAGGAGGCTGAGG	100507650
rs748465609	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206910	GAAAAACAAACTTTC[A/G]TTAAAAAAAAAAAGA	100507650
rs748620097	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23250256	AGGCTGAGGGGGTGG[A/T]TCACTTGAGGTCAGG	100507650
rs748625479	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23193671	TGAGGCAAGTATTAA[-/C]TTCAAGGAATTGTTT	100507650
rs748713337	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23218157	GCGGATCACGAGGTC[A/G]GGAGATCGAGACCCT	100507650
rs748734342	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23220894	AAGCATACCACCAGA[A/G]AAAATCACCTTCACT	100507650
rs748739470	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206391	TCTTTTCTTTTTCAG[C/T]ATCTGATTTACATGC	100507650
rs748785974	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209104	GATATGCTAAACAAG[C/G]GGTGGATTATTCATG	100507650
rs748940095	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23271958	TCTCTTTTATAGGTA[C/T]ATACTAAAGTATTTA	100507650
rs748981201	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23258066	AAAAGGGGCCGGGTG[C/T]GGTGGCTCACGCCTG	100507650
rs748989337	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212576	ATTTTATTTTATTTT[A/G]TTTATTTATTTATTT	100507650
rs749079907	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213484	ATTCCACCAGGAGTC[A/C]TGAGGCGGAAAGAAG	100507650
rs749122528	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23187604	TTCCTGATTTTTTTT[C/T]CTAGATCCAATAGAC	100507650
rs749140751	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23264095	TCTGTCTGAAAAAAA[A/C]CAAAACAAAAAAACA	100507650
rs749163130	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23247730	GTAATATTGCTATGG[A/G]ACATTTATGTACAAG	100507650
rs749164528	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23267963	TAATTACAGATAAGG[A/T]AGGACTGACTTCTGC	100507650
rs749186005	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201729	TAGGATTTCAGGTCA[C/T]TGTAAAGTCATCTGT	100507650
rs749302930	in-del	-/GC	0.000489656	0.0156393	intron-variant	RNF212B	GRCh38.p7	14:23262883	AGGCAAGGCAGGCAT[-/GC]ACCATTGATGGCAAC	100507650
rs749385252	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23254178	TTGTCCCAGCTACTC[A/G]GGAGGCTGAAGTGGG	100507650
rs749399314	snp	A/C/T			intron-variant	RNF212B	GRCh38.p7	14:23220621	ACGAGGTCAGGAGAT[A/C/T]GAGATCACCCTGGCT	100507650
rs749418128	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208020	ATCAGATATGCATCT[A/G]TATCAGTGAGTACAG	100507650
rs749460652	in-del	-/TGA			intron-variant	RNF212B	GRCh38.p7	14:23268600	CTAGCTAATTTTTGT[-/TGA]TGATGTCACTCCTAG	100507650
rs749473129	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23252805	TAAGCAACTTTTAAG[-/C]AAAAGCCTTATGATT	100507650
rs749528130	in-del	-/TAGAG			intron-variant	RNF212B	GRCh38.p7	14:23257399	TTTAAAAAAATAGAC[-/TAGAG]TAAATTCTTATCTAT	100507650
rs749551965	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23225051	TGAAACTACAGTGAT[C/G]AGATTAAGACACCTT	100507650
rs749565750	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204146	TCAGATGGATAGATT[A/G]TGAAGATTTTCTCCC	100507650
rs749576966	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23254679	GATTACAGGCATGAG[A/C]CACTGCACCTGGCCT	100507650
rs749581014	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23241233	GAACAGCATGTACAA[A/G]GACATATTACATCAC	100507650
rs749611096	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196125	AAACTTCCTTATGAA[C/T]GGGAGCACCTGGCTT	100507650
rs749675083	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197087	GCTGAATGAATGTAT[A/T]TAGGACATGTATGTG	100507650
rs749679746	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23240308	TAATTATGTTATTCT[C/T]TAGGTTATTCTTACT	100507650
rs749689284	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23226045	TGGCTCACGCCTGTA[A/G]TCTCAGCACTTTGGG	100507650
rs749692200	snp	A/G	0.000229489	0.0107094	missense, utr-variant-3-prime, stop-lost, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270638	CTAGAGAGTCTTCCT[A/G]GTTTCCAGCTACCAG	100507650
rs749737865	in-del	-/A/AA			intron-variant	RNF212B	GRCh38.p7	14:23223057	AAACTCCGTCTCAAA[-/A/AA]AAAAAAAAAAAAAAG	100507650
rs749772409	in-del	-/AGA			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213735	AAGAAAGAAAGAGAG[-/AGA]AGAAGTGAGGAAGAG	100507650
rs749789778	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23261520	CAGTCATTTCCTCTG[C/T]GAAGACTGCATTAGG	100507650
rs749842414	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215968	ATTAAAACATTTGCC[A/G]GGTGTGGTGGCTCAT	100507650
rs749851498	snp	A/C/G	0.000115201	0.00758862	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23268938	GAAACCCCTTCACCG[A/C/G]CTTCAACTCATAGCC	100507650
rs749886637	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195619	TCTTCCAACACTCCC[C/T]GGACCTCCACACCTC	100507650
rs749891528	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23263858	TTTGGGAGGCTGAGG[C/T]GAGTGGATCATTTGA	100507650
rs749902085	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229827	GCGCACAGCAAATAA[A/G]GAAACAGAAAAACTA	100507650
rs749920388	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23247512	GAATCATATAATGTA[C/T]GGTCTTTTGTGACTT	100507650
rs749923713	snp	C/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199459	TTGCCCTAAGCAGTT[C/T]CCAGCTTGACTATTC	100507650
rs749927744	in-del	-/CCAGCTGCT			intron-variant	RNF212B	GRCh38.p7	14:23261848	AGGACACCTGTAGTC[-/CCAGCTGCT]CGGGAGGCTGAGGCA	100507650
rs749932102	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23228767	GTGACAGTATGGTAT[G/T]GGCATCAAGACAGAC	100507650
rs749941523	snp	A/C			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185490	TTTCTGCTTCTTAAA[A/C]GTGAGTTCTTTCAGT	100507650
rs749952228	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218026	TCTATTAGATACATT[C/T]AACAAAGAGATTGAA	100507650
rs749978353	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193925	TGGCTCACTGCAACC[C/T]CCGCCTCCTGGGTTC	100507650
rs749994999	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23186763	GACGAGGCAGTTATC[G/T]TAAAGATTTTAAAAA	100507650
rs750170949	snp	C/G/T			intron-variant	RNF212B	GRCh38.p7	14:23253531	TCATTGGTTTGGGGG[C/G/T]GGGGAAAGGTGAGGC	100507650
rs750186348	snp	A/G			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207409	AGTTACCTGCCTTTC[A/G]TCGTCATGGAAGGAG	100507650
rs750191821	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23255970	TGCTGGTTGTTTTCT[A/G]GACTGGTCTTTCTTC	100507650
rs750200543	snp	A/G	0.000122093	0.00781226	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269981	TTAAATAACATTTCC[A/G]AAGGAATGGAGCTTC	100507650
rs750208377	in-del	-/AAA			intron-variant	RNF212B	GRCh38.p7	14:23218368	GTGAGAGTCTATCTC[-/AAA]AAAAAAAATAAATAA	100507650
rs750267125	snp	A/G			splice-acceptor-variant, intron-variant	RNF212B	GRCh38.p7	14:23240343	CTCTTTATCTGCTCC[A/G]GAATGGATTGGTTTC	100507650
rs750268370	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23194671	GCCCGGGAGATGGAG[G/T]TTGCAGTGAGCCGAG	100507650
rs750289866	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23255996	TCTTCTTCTTGGAAT[-/G]ATCAGTTTTTTGGGA	100507650
rs750323292	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195655	AAACCTGTGCTCTCC[C/T]GACAGCACATCCACC	100507650
rs750398680	snp	A/G			missense, intron-variant, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23260672	AGGAATCTCCAAGTC[A/G]GTACCAAGGAAGCAG	100507650
rs750429657	snp	C/T	0.000363967	0.0134852	missense, intron-variant, synonymous-codon, nc-transcript-variant	RNF212B	GRCh38.p7	14:23264175	TTCACCTTATACAGT[C/T]GGTCCTCCTCAGCGG	100507650
rs750438069	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23224193	AGATTCAATGCAATT[C/G]TTATCAAAATACCGA	100507650
rs750481901	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201336	TGACAAAAAGTTTTA[A/G]GGCAGCCATAGTCAA	100507650
rs750498907	snp	A/G	0.000112937	0.0075137	intron-variant	RNF212B	GRCh38.p7	14:23243216	TAAATCTTACCTCAT[A/G]CTCATGAGAGCCAAA	100507650
rs750528223	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214437	AGGTGGAGGTTGCGG[C/T]GAGCCCAAATTGCGC	100507650
rs750542650	snp	G/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215216	CTGTTGTCATGTAAG[G/T]TGTGCCTTGCTTCTC	100507650
rs750617823	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202965	AAGGACTTTATTTTA[C/T]TTCATTTTATTTTGT	100507650
rs750680131	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23249352	GGGGTTTGAGACTAG[C/T]TTGGGCAACATAGTG	100507650
rs750686282	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23234935	ATTAAAAATTAGGGC[A/T]GGGTACGGTGGCTCA	100507650
rs750760701	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23221141	CCTATAATCCCAGCA[A/C]TTTGGGAGGCTGAGG	100507650
rs750775625	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23268043	TTGTCCCAGCTGATA[C/T]TTATCTCCTTAGGCA	100507650
rs750810819	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212638	CCAGGCTGGAGTGCA[A/G]TGGCGCAGTCTCGGC	100507650
rs750853399	in-del	-/GGCAGTGGTG			intron-variant	RNF212B	GRCh38.p7	14:23217246	AGTGGTGGCAGTGGT[-/GGCAGTGGTG]GGCAGTGGTGGGGGG	100507650
rs750856664	snp	A/G	0.000121974	0.00780845	missense, utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23258588	ACAGATCTCCTCATC[A/G]CCTTTTATAAGCATA	100507650
rs750942832	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23269072	CACTTTGGGAGGCCG[A/T]GGAGGGTGGATCACT	100507650
rs750959723	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23242891	GGCTGAAGCAGGAGG[A/T]TCACTTGAGCCCGGG	100507650
rs750972159	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23227161	CAAGGGTATATGGAA[C/T]CTTTCTACACTACTT	100507650
rs751035837	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23255973	TGGTTGTTTTCTGGA[C/T]TGGTCTTTCTTCTTC	100507650
rs751066954	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23266150	TTTTAGTAGCGACGG[A/G]GTTTCACCATGTTGG	100507650
rs751100006	snp	G/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214430	ACCCAGGAGGTGGAG[G/T]TTGCGGTGAGCCCAA	100507650
rs751116175	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23227517	AGAAATAGGCATACT[A/T]CTGTATGTATATTAT	100507650
rs751172498	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198295	CTTACATAACTCAAG[G/T]CCATTATCACACCTA	100507650
rs751223369	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23228719	GAGGATCAAGACTAC[A/C]TCATTTCAAGACTTA	100507650
rs751227037	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23263718	CATCAATCCAGCTTC[A/G]GAGACTTTCTATTAG	100507650
rs751232750	in-del	-/CAAAA			intron-variant	RNF212B	GRCh38.p7	14:23220233	AAACAAAAACAAAAA[-/CAAAA]ACCATACAACAAGGC	100507650
rs751297270	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23255242	TTAATCAGAACACTC[A/G]TTCTGTGTTTTAGAA	100507650
rs751309104	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204766	TCTATGAAGAATGAT[C/G]GTGGTATTTTGATGG	100507650
rs751332032	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23250877	ATAGGTAGATAAGAG[A/G]CCAATGGTTGCCTTC	100507650
rs751341489	in-del	-/AAAAAAAAAAAAAAA			intron-variant	RNF212B	GRCh38.p7	14:23233570	ATCTCTACAAAAAAA[-/AAAAAAAAAAAAAAA]TAGAAAAATTAGCCG	100507650
rs751352848	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23217928	AGAAACAGGGATATA[C/T]GACTTTTGAGGCAGA	100507650
rs751381455	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202604	CGCCTGTAATCCCAG[A/C]ACTTCGGGAGGCCGA	100507650
rs751385126	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23253832	AAAAGATAGATAAGG[-/C]AAACTAATAGGTTTT	100507650
rs751574221	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23272761	ACAACAGGTCAGAGA[G/T]ACTTGCTTGCCCTTT	100507650
rs751579140	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23223501	GCTGGACTACAGGCG[C/T]CCGCCATCAAGCCCG	100507650
rs751589971	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23239257	TAGAGACGGAGTTTT[C/G]CCACGTTGGCCAGGC	100507650
rs751599565	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213336	AAAAAATTATAAAAC[C/G]TTACTGAGAGAAATT	100507650
rs751646349	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23239867	CAGGTGATCCACCTG[C/T]CTCGGCCTCCCAAAG	100507650
rs751698384	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23224111	CACACAAAGGAAAGA[C/T]ATTTCATGTTCACGG	100507650
rs751712011	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23189090	AGATCTCAAGCAGGC[C/T]CTTAACACTGCCAGC	100507650
rs751733833	snp	C/T			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199765	AATCTATATAGGCCA[C/T]ATTTCTCTGAAGTCT	100507650
rs751756857	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214262	ATTTTGGGAGGCCAA[A/G]GCAGGTGGATCATTT	100507650
rs751758058	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23258880	TTTCCTCTTCTATTT[C/G]TCGGTATCAAAAACT	100507650
rs751799882	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212339	AAGAAGGAAAACTGT[A/T]TTTCTTTTTTTGAGC	100507650
rs751886095	snp	G/T	0.000124743	0.00789657	missense, nc-transcript-variant	RNF212B	GRCh38.p7	14:23258660	GCACTGGTGAGCCAG[G/T]ACAAGTAAGTAACAA	100507650
rs751891217	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201067	AAGACTCTGAAAAAC[A/G]GAATAAAGGATCAGC	100507650
rs751895905	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210505	AGGATGGGGTGGGCG[C/T]GGTGGCTCACGCCTA	100507650
rs751899373	in-del	-/CGCCACTGCA			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236471	AGTGAGCCGAGATGG[-/CGCCACTGCA]CTCCAGCCCTGGCGA	100507650
rs751968496	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23188280	GTGGGAAAGAAATAA[A/C]GAGGCACTGCCTGTG	100507650
rs751988750	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266975	TTTGGTTTTTTGTTT[C/T]CTTGTTTTTTTGAGA	100507650
rs752022188	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23189465	TTTCACTGTCTCCTG[A/G]ATTATTCCTGTCAGC	100507650
rs752074586	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23253722	GGAGTACTTCTAAAG[A/G]GAAATGTCCTTTTAT	100507650
rs752110200	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23248892	ACAAATATTCAGACC[A/G]CAGCAGGCCAGTAAA	100507650
rs752177234	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267796	TTTGTTCCTTGTTTT[C/T]TGCATGGAATATATT	100507650
rs752272257	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209890	CAGTGAGGTGACTCA[A/G]ACCTGTAATCACAGC	100507650
rs752310570	in-del	-/TTTTT			intron-variant	RNF212B	GRCh38.p7	14:23258694	AAGTCCCAAGAGAGC[-/TTTTT]TTTTTTTTTTTTTTC	100507650
rs752365062	snp	A/G			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274627	TAAGAACTGAAAATA[A/G]CCGGGCACGGTGGCT	100507650
rs752420034	snp	G/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183811	ACTGAGAAAATGGAC[G/T]AAGTTATTTCTTTTT	100507650
rs752428040	snp	A/C			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215654	TAGGAATAAGGTGAA[A/C]TCAAGACATTCCCAA	100507650
rs752443844	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23251998	AGGAGTTGTTATGAA[C/T]GTTCCATTACATAGG	100507650
rs752562449	in-del	-/AA			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194734	GTGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA	100507650
rs752564481	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23249612	ACCTAAAAAGGAAAA[A/G]CTTTCAGTATTTAGG	100507650
rs752575668	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184871	GCATGAAGCAATATA[A/G]TGGACAACACTATAA	100507650
rs752635284	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204445	ATTCTCCTACCTGTG[C/G]CTAGCCAATTATCCC	100507650
rs752668268	snp	A/C			utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23238045	TTTCTGGAATCACAG[A/C]GGCCAAGCGGGTAGG	100507650
rs752722173	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23250691	TTATTTTGCCAAGAT[C/T]GAGGACATGCGCCTC	100507650
rs752816104	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23190877	GTGGTCCTCCAGTCT[C/T]ATAGGCCTCCTTCCT	100507650
rs752825390	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23239127	GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC	100507650
rs752871088	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23193510	GGACTCAAGAGGATG[A/T]CTCCCAGAAAATAAA	100507650
rs752927075	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23224589	TAGCTCTTGCCCATA[A/C]ACAAAAGTCAAATCA	100507650
rs752942662	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185283	AAAAAACCAGACAAG[A/G]CAGGGAATATATAGC	100507650
rs752949101	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23258509	GTGAAGGGAAAGGAG[A/T]TATGGGAGAGTATGT	100507650
rs753025862	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198588	AGCTGAAGCGGGAGA[A/G]TCACTTGAACCTGGG	100507650
rs753047900	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23223381	TTTTTTTTGAGATGG[A/T]GTCTTGCTCTGTCGC	100507650
rs753075947	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23186999	GATCCTAACACTTAT[C/G]TGCTCAGTGAGACCC	100507650
rs753080467	in-del	-/CAAAAC			intron-variant	RNF212B	GRCh38.p7	14:23254292	TCTTTATCTCAAAAA[-/CAAAAC]AAAACAAAACAAAAC	100507650
rs753140755	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23228897	ATTTGCTATTTTAAC[C/T]ATTGTTAGTGTGCAA	100507650
rs753166861	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200571	CCTCAAGTGATCCAC[C/T]CACCTCGGCCTCCCA	100507650
rs753198701	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23193659	CAAATGAAAACATGA[A/G]GCAAGTATTAACTTC	100507650
rs753229837	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195435	TCACCATATCTCTTG[C/T]CTACCTCTAAGGCTT	100507650
rs753281656	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23266864	CGTGTTGTTCAATTA[C/G]TATGCTTCTGTTTCC	100507650
rs753285978	in-del	-/AG			intron-variant	RNF212B	GRCh38.p7	14:23193118	AAAAAAAAAAAAAAA[-/AG]AATGTTACCAGAATG	100507650
rs753371777	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23253600	TACTTAATGGTCTAT[C/G]TCTCTTATTTTGTAT	100507650
rs753399577	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207632	GATAGGAGATTTGTC[A/C]AAGGTCGGGGGCAAC	100507650
rs753470758	snp	A/T	0.00133309	0.0257831	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240424	TGTGGCCATATTTTC[A/T]GTAAAAAGTGTGTGA	100507650
rs753558804	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23224413	CCAGACACATAGACC[A/G]ATGGAACAAACTAGA	100507650
rs753565351	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195792	ATGTAACAAGGAATT[G/T]CATCATGTTTAATTT	100507650
rs753592478	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23218888	GAAGAGTACCTCCGG[C/G]CATTTAATAATCAAA	100507650
rs753602246	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23254791	CTAAGCTCCCCCTTT[-/G]CTTCCATTACTGTGC	100507650
rs753632725	in-del	-/GGGGGGTCAGCCCCCGCCCGGCCAGCCGCCCCGTCCGGGAGGGAGGTG			intron-variant	RNF212B	GRCh38.p7	14:23232690	GTCTGGGAGGGAGGT[lengthTooLong]GGGGGGTCAGCCCCC	100507650
rs753644788	snp	C/G			utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274163	CCATATAGCTGATCC[C/G]AACTGATGAAAACCA	100507650
rs753671292	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23225416	AACTTAAGTGTCCAT[C/T]AACAGATGAATGGAT	100507650
rs753775213	snp	A/C			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215376	TTTCCTATGGAGAAA[A/C]AAAGATTCAAATGAC	100507650
rs753787383	in-del	-/TAATAA			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205028	AAGCAAACCAAAACT[-/TAATAA]TAATATTTGGACTTT	100507650
rs753788853	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260809	AGCTTTCACTTCTCC[A/G]AGGAAGAGTTAGTTA	100507650
rs753817475	in-del	-/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203484	CTTTTAGTCCCCCTT[-/T]TTTTTTTTTTTTGAG	100507650
rs753825361	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23257677	TATTAACTTTTGATC[C/T]GATTCAGCAATCCCA	100507650
rs753866625	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23233279	CACTGCGGAAGGCCG[C/T]AGGGTCCTCTGCCTA	100507650
rs753885365	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206816	AAGAGTAGCCTCTGT[A/T]GCAGTAACTATTTTA	100507650
rs753916254	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23189638	CAAAACCTTGTTTCT[A/G]CTAAAAATTAAAAAA	100507650
rs753935079	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203053	GTTCTTTAGTGGTGA[A/T]TTGTGAGATTTTGGT	100507650
rs753946193	snp	A/G			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236137	TTAAGCTACATAGCA[A/G]GAGATTACAAAAATG	100507650
rs753986573	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23223239	AAAGTTCAATGTCAC[C/T]TCATGACAAAAAAAC	100507650
rs754025901	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204119	TTGTAGATTCCGGAT[A/G]TTAGTCCTTTGTCAG	100507650
rs754086831	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23271073	TTTATAAATTTATGG[C/G]ACTATGATTCTGATT	100507650
rs754150836	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221957	GATAATGGAAACACA[A/G]CATACCAAAACCTAT	100507650
rs754159195	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193581	ATAGTACCCAGGGGG[C/T]GGATTTATGTTTTTA	100507650
rs754185220	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23256142	CAAAGGGAGGGCTAA[C/T]TAATCTAGGGTAGGA	100507650
rs754216113	in-del	-/AC			intron-variant	RNF212B	GRCh38.p7	14:23239995	AAAGTAAAGGAAAAC[-/AC]ACACACACACACACA	100507650
rs754281346	snp	C/T			stop-gained, utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23244373	GTGGAGACAGCTTTG[C/T]AGTATTTTAGTCACA	100507650
rs754364658	snp	C/T	0.000121499	0.00779326	synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240441	TAAAAAGTGTGTGAC[C/T]CTGGGTGAGTGACTC	100507650
rs754375070	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207641	TTTGTCAAAGGTCGG[C/G]GGCAACTCCACTCAG	100507650
rs754405824	snp	C/G	0.000110211	0.00742249	intron-variant	RNF212B	GRCh38.p7	14:23264709	TCAGAAATCAACTTA[C/G]TCTATGCGAAGATCT	100507650
rs754409282	in-del	-/TTTT	0.00591711	0.0540698	intron-variant	RNF212B	GRCh38.p7	14:23258694	AAGTCCCAAGAGAGC[-/TTTT]TTTTTTTTTTTTTTT	100507650
rs754463131	snp	A/G			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23195162	GCCAGGTGTTGTGGT[A/G]CACGTCTACAGTCCC	100507650
rs754523027	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23254834	TTTTCAGTTATTTCT[C/T]CTTTACTCTTTCCAA	100507650
rs754529677	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23239370	TGGCCTGATTCTGAG[C/T]TTCTGCAGAAGAAAA	100507650
rs754531372	snp	G/T	0.000116435	0.00762914	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270558	CACTGCCGAGAAACT[G/T]CCCAAGTAAGTTATC	100507650
rs754608772	snp	A/C			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273166	ATTTGGAACAAAGGT[A/C]AAAAAAATAATTCTT	100507650
rs754617819	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23240581	ATACTGTAGGAAACT[A/G]TCAATTTTAGAAATT	100507650
rs754695042	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195809	ATCATGTTTAATTTC[A/G]TTTAACCTTCCAAAC	100507650
rs754702415	snp	C/T			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274305	AAGATGAAAAATTAG[C/T]CTCTGTCAAGCTGGA	100507650
rs754757984	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229976	TTATAGATCCAGCTT[A/G]AATCTTCTCCAATGT	100507650
rs754803548	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195267	ACTCTGTCTCTAAAG[-/A]AAAAAAAAAAACCCA	100507650
rs754845229	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215486	TTCTAGCCTGGGTGA[C/T]AGAGCAAGACTCTGT	100507650
rs754850068	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23270918	AGAGGTCTTGGCCAG[C/T]GTGAAGTAAGTGTGG	100507650
rs754871862	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23234995	GAGGCAGGTGGATCA[C/T]GAGGTCAAGAGTTTG	100507650
rs754940846	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201779	AAGGATTTCAAAAAT[A/G]GTGAAAACCTTCATT	100507650
rs754951252	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23249502	GTGAGCCATGATTGC[A/C]CCACCATACTCCAGC	100507650
rs755030549	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203110	TGCACCCTATTTGTA[G/T]TCTTTTATCTCTCAT	100507650
rs755033382	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236188	TCACTAAATTTTTCT[C/T]GTTTTGGAAAACATA	100507650
rs755095572	snp	A/T			missense, synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269886	CTGCCTCCTCTGGAC[A/T]GGGGATTTTTTCTTT	100507650
rs755122389	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208922	CGCCACTACGCCTGG[C/T]TAATTTTTTGTATTT	100507650
rs755183295	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23256163	TAGGGTAGGATTTGG[C/T]TTATCTTGATGCTAG	100507650
rs755245355	snp	G/T	0.190528	0.242823	intron-variant	RNF212B	GRCh38.p7	14:23258695	AGTCCCAAGAGAGCT[G/T]TTTTTTTTTTTTTTT	100507650
rs755250472	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210414	GAAAATGAGATTTGA[A/G]CAAAGTCTGGAGTTT	100507650
rs755369863	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23222000	AAACAGTATTAAGAG[A/G]GAAATGTATAGCTAT	100507650
rs755385965	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23265698	TCTTTTCCTCTTTCT[C/T]TGTCAATCATTTCAA	100507650
rs755426143	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23190864	CTCTTCCTTTCACGT[A/G]GTCCTCCAGTCTCAT	100507650
rs755439302	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244422	CAAAAGTGAAGAAAA[C/T]CTGACTCTCCAGGCA	100507650
rs755493700	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23263879	GATCATTTGAGGTCA[A/G]GAGTTCGAGACCAGT	100507650
rs755510984	in-del	-/AC			intron-variant	RNF212B	GRCh38.p7	14:23238542	AGACCAGCCTGGGTA[-/AC]ACAGAGAGGCCTTGT	100507650
rs755520743	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23217107	TGAACCTGCTATGGA[C/G]CAGAGTGGAGCCCCC	100507650
rs755534345	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23245870	GTTGGTTTTGCTTAT[C/T]GTTCTCTTTTAATAG	100507650
rs755536821	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23263492	TGGTAATCAATGACT[A/G]GGGGTCAGGTCCTAA	100507650
rs755552974	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23228811	GAACAGAATAGAGCA[G/T]GCAGAAATGGGCTTG	100507650
rs755562003	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23186873	ATAGTTTACACTGAG[C/G]ACTTTTTCAGGATGC	100507650
rs755662650	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23247554	TAAGTATAATGCTCT[C/G]AAGTTTCATCCATGT	100507650
rs755690172	snp	C/G	0.000114936	0.00757989	missense, synonymous-codon, stop-gained, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270602	TTCTATCCTTCAGCT[C/G]AGAGGGAGAGCACAA	100507650
rs755698471	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206305	GTCTTGAACTCCTGA[C/T]CTCTTGATCCACCTG	100507650
rs755775487	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23252405	ATTATGATTTCATCA[C/T]ATGTAATTTCAAATG	100507650
rs755798406	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23239336	AAGTGCTGGGATTAC[A/G]GGTGTGAGACACCAT	100507650
rs755805706	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193920	GATCTTGGCTCACTG[C/T]AACCTCCGCCTCCTG	100507650
rs755812573	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23242448	GAGCTTCAAAGCAAG[-/A]TTAACAAATATTAGC	100507650
rs755855643	snp	G/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194955	TCTAGAAATTTCAAA[G/T]ATGTGAAATCATACA	100507650
rs755860710	snp	C/T			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207430	ATGGAAGGAGGAAAA[C/T]TTGCCTTCCTGTTGG	100507650
rs755915040	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23271892	TAATTGTTAACATTG[G/T]AGAGTTTTTTGGTAT	100507650
rs755929811	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23273047	TACCCTATTCACCCT[C/T]ATCACCTCCCAGGAC	100507650
rs755944227	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23259164	CCACGACACTCCAGC[A/G]TGGGTGAAAAAGTGA	100507650
rs756088930	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213440	TTTTTCCCAATTTGA[A/T]CTATAGATTCAATGC	100507650
rs756103857	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260752	TCTTTCTTGACTCCT[A/G]GCTGTGTGAACTCTG	100507650
rs756150878	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201437	GTTATTGATAATGTA[C/T]ACTAAGTTATATTAG	100507650
rs756167861	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203047	AACTGAGTTCTTTAG[C/T]GGTGATTTGTGAGAT	100507650
rs756184962	in-del	-/ATCATCATC			intron-variant	RNF212B	GRCh38.p7	14:23238777	ATAATAATAATAATA[-/ATCATCATC]ATAATCCCACAAAGA	100507650
rs756231647	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23248367	GAACCCCTGGGCTCA[C/T]GCAATCTGCCCGCCT	100507650
rs756327857	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211218	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAGAAAG	100507650
rs756345901	snp	A/G			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236133	TCTATTAAGCTACAT[A/G]GCAAGAGATTACAAA	100507650
rs756396430	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209236	GTCACTCTCGTAGCC[A/G]TTTTGGTTTTGGTGG	100507650
rs756433312	in-del	-/AA			intron-variant	RNF212B	GRCh38.p7	14:23223053	AGTGAAACTCCGTCT[-/AA]CAAAAAAAAAAAAAA	100507650
rs756583798	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23263201	ACAACTCTCAAACTC[C/T]CTTCTTCAATGGATT	100507650
rs756585604	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23254595	GATAGCATTTTGCCA[C/T]GTTGCCCAGGCTGTT	100507650
rs756604644	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23188188	ATCCTTGCTCTGACA[A/C]CAGAGACAAAAATTC	100507650
rs756633089	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23242952	CCACTGCATTCCAGC[C/T]TGGGTGATAGAGTGA	100507650
rs756675475	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195976	CTTTTCACTGTGCCA[C/T]GGGAGAAAAAAGGTA	100507650
rs756677917	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23227711	CTCAAGAGATTCTCC[C/T]ACCTCAACCTCCTTA	100507650
rs756751399	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197009	ATGGTGCTTTTTTTG[C/T]TCACTAATGTCTTCA	100507650
rs756767752	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198297	TACATAACTCAAGGC[C/T]ATTATCACACCTAAT	100507650
rs756779781	snp	A/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184142	GGGAAATGGAAGGAA[A/T]TAACAATGGGAAAAA	100507650
rs756782427	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23262148	AAGCCCATTACAACA[C/T]TTAAACACTGTTCTG	100507650
rs756800986	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23250074	AAACACAAGTTATTA[C/G]GTAAGGTTATTTATT	100507650
rs756832777	snp	C/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23185143	AGCAGTCATCTGCCC[C/G]CTTGATCACTCAGCA	100507650
rs756872928	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23217016	TGTTAAGAATGGGGA[C/T]AGGCACAGAAGGGTA	100507650
rs756894075	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23245418	AAGAGAAAGAGCAGA[-/C]CTTTAGTTAATAAAT	100507650
rs756949787	snp	A/G	0.000122707	0.00783188	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23259902	ATTGTCAGTCTTAAG[A/G]AAGGAGAATGGAGAA	100507650
rs756962822	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23217970	AGCTGTTTTAAGGAA[C/T]TCAAAAAAATTCAAG	100507650
rs756962988	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204778	GATGGTGGTATTTTG[A/G]TGGGGATTGTGTTGT	100507650
rs756963405	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23250879	AGGTAGATAAGAGAC[C/G]AATGGTTGCCTTCTT	100507650
rs756988674	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23218793	CAAAGGATTATATCA[A/G]AGAACTTCCTAAACC	100507650
rs757034964	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23191159	AGGAGTTCAAGACCA[G/T]CCTGGCCAACAAGGC	100507650
rs757045926	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23187119	GTTTCCAATATCGGA[-/G]CCACTGTTTCAGCTG	100507650
rs757076338	snp	A/G	0.000121087	0.00778004	intron-variant	RNF212B	GRCh38.p7	14:23263001	AACATTAAAACTGTT[A/G]GCAAAAGTTGGAAGA	100507650
rs757083012	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23252387	CCCATTAAAAAAAAG[C/T]TTATTATGATTTCAT	100507650
rs757086849	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23271761	AAAGCTCTATAAACC[A/G]TCTACAAATATATGG	100507650
rs757094076	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23230203	ATATTTTGAATATTA[A/G]AACCTTATCAGATAT	100507650
rs757169522	snp	A/G			utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23238051	GAATCACAGCGGCCA[A/G]GCGGGTAGGGAGTGT	100507650
rs757239623	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272773	AGAGACTTGCTTGCC[C/T]TTTTTGCTGTTATAA	100507650
rs757257525	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23222407	GGATAAATTTTTAGA[A/C]ATATACAACCTACCA	100507650
rs757262892	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23220295	TCAGCACTTTGGGAG[G/T]TCGAGGTGGGTGGAT	100507650
rs757321275	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213354	ACTGAGAGAAATTAA[A/G]GAAGACCTAAATAAA	100507650
rs757394991	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23227044	TAAGACTAATGAAAT[-/C]AGTAATGTCATGAGG	100507650
rs757427214	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23230163	TGGTGGAAAAAGGAA[A/G]AGAGAGAGAGTTGTA	100507650
rs757444730	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23268907	TATCTCACAGGCTTA[-/T]TTTTTATGCTTTCCA	100507650
rs757488499	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201122	AGATTAGTTCAGTCC[A/G]TGCAGTTAATTCCTG	100507650
rs757509930	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23187234	TTTAGAAAGAGAAAG[C/G]CTGTGCGTAGCTGAC	100507650
rs757517417	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23219345	AGAAAGACTAAATGA[C/T]GAACTAATAAAAAAT	100507650
rs757567886	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23188337	ATTCTTTTGCTGGGT[C/T]CAATCTGTCATGGGG	100507650
rs757576227	snp	G/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260735	CCCCTGAAAATTCCT[G/T]TTCTTTCTTGACTCC	100507650
rs757696300	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23225567	GGCACAGAAAGACAA[A/C]CATTTCATGTTCTCA	100507650
rs757701827	in-del	-/TTC	0.0366447	0.130305	intron-variant	RNF212B	GRCh38.p7	14:23258710	TTTTTTTTTTTTTTT[-/TTC]TTCTAAGAAGTGACA	100507650
rs757718520	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209048	CAGGCGTGAGCCACC[A/G]TGCCCGGCCTGGTTG	100507650
rs757723889	in-del	-/AAAAACAAAAAC			intron-variant	RNF212B	GRCh38.p7	14:23220186	CAAAACTGTCTCGGG[-/AAAAACAAAAAC]AAAAACAAAAACAAA	100507650
rs757734574	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23254467	TCTATCAAAATAAAA[A/G]TAAATAAAAATAAGA	100507650
rs757765815	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23240740	TTCTTCAGGGAAAAG[A/G]GATAGAATAAGTATA	100507650
rs757781657	snp	C/T	0.000122496	0.00782517	intron-variant	RNF212B	GRCh38.p7	14:23240470	TCAACTGTTTTCAGA[C/T]TCAGGGAAAAATGTT	100507650
rs757811701	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207797	CAACATGTGCCCAAG[G/T]TGGTCGGGGTACAGC	100507650
rs757827872	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267876	GTATCTTGTAGACTG[C/T]GCATAGTTGGACTTG	100507650
rs757929733	in-del	-/AAAAAC			intron-variant	RNF212B	GRCh38.p7	14:23220192	TGTCTCGGGAAAAAC[-/AAAAAC]AAAAACAAAAACAAA	100507650
rs757952234	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23242677	TGGGAATTTATAAAA[A/C]GATGGGGCAGGAGGT	100507650
rs758005807	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196894	CCTGGCCCTAGAGTG[G/T]GTTCTTTGTTTCAGA	100507650
rs758014893	snp	A/G			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274775	GCCGGGTGTGGTGGC[A/G]GGTGCCTGTAGTCCC	100507650
rs758082825	in-del	-/AAA			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211218	TGAGACTCTGTCTCA[-/AAA]AAAAAAAAAAGAAAG	100507650
rs758135334	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183908	AACTGTTCCGGGAGA[A/G]CTCATTAGCTAGTAT	100507650
rs758144244	snp	A/C	0.000122167	0.00781465	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269987	AACATTTCCAAAGGA[A/C]TGGAGCTTCAACTAT	100507650
rs758249343	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204571	TTCTCTATTCTGTTC[C/T]ATTGGTGTATGTACC	100507650
rs758261780	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236463	GAGGTTGCAGTGAGC[C/T]GAGATGGCGCCACTG	100507650
rs758280263	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23221479	CCCAATGCTAGAGTA[A/C]CCAGATATATAAAGC	100507650
rs758358670	snp	A/G			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270111	TTTAAGAGCCATCCC[A/G]TTTTCTTCAGAGTGA	100507650
rs758368527	snp	C/T			utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23237939	GCTGCGCCCAGCCTC[C/T]TTCCTCACCCGGTGC	100507650
rs758400831	in-del	-/CCCATA			cds-indel, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273704	ATCTGAACTAGGATC[-/CCCATA]CCCTTTCTGGTACTC	100507650
rs758406649	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23250807	ATATGTATGATGAAC[A/G]TTGGTTCGATCGGGA	100507650
rs758449438	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23217320	ACTTTATATTGTGGT[G/T]TGAGTGCCAGCTTAG	100507650
rs758452982	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193602	TATGTTTTTATCTAA[C/T]GAGTCTAAGAAGAAC	100507650
rs758510981	in-del	-/T	0.00514177	0.0504425	intron-variant	RNF212B	GRCh38.p7	14:23262647	GATTAGAGCCGCCTC[-/T]TTTTTTTTCCCTTGC	100507650
rs758512815	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23271370	ATTGCTTGAACCCAG[G/T]AGGCGGAGCTTGCAG	100507650
rs758537903	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23257753	AAAATTACGTGTGCA[C/T]GCCCAGAAAAAAAAT	100507650
rs758646142	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23185906	GGAGTTCAAGACCAG[A/G]CTGGGCAATGTGGTG	100507650
rs758707686	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23227494	AAATTCAGTAAGCTA[-/T]GTGTGCAAGAAATAG	100507650
rs758799011	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23187115	TTCTGTTTCCAATAT[C/T]GGAGCCACTGTTTCA	100507650
rs758928928	snp	C/G			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270086	GTCTCTAGTTGGCTC[C/G]TTAATATTCTTTAAG	100507650
rs758952031	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205019	TTTTTTCCTAAGCAA[A/G]CCAAAACTTAATAAT	100507650
rs758999233	in-del	-/TT			intron-variant	RNF212B	GRCh38.p7	14:23258695	AGTCCCAAGAGAGCT[-/TT]TTTTTTTTTTTTTTT	100507650
rs759022795	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23189369	ATCTCCCCTATTTGT[A/G]CACTAGCTTCCCTAT	100507650
rs759080014	in-del	-/A	0.000188271	0.00970051	utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272914	CAAGATCTGATCTAT[-/A]ACATGCTGCTGAAGG	100507650
rs759088744	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201824	ACTTAATTTTCTAAA[A/C]CTGAAGCCCTAATAA	100507650
rs759150446	snp	C/T	0.000121514	0.00779373	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240347	TTATCTGCTCCAGAA[C/T]GGATTGGTTTCATTG	100507650
rs759180844	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209804	GATATATGGATATCA[C/T]GTACCCCTGATACAA	100507650
rs759186271	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23254356	AACTAAAACTAAAAC[C/T]GGGCATGGTGGCTCA	100507650
rs759197787	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196819	CCTAGTTCACTGCTA[C/T]TCATCCTTCTGATTT	100507650
rs759198535	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23242380	CAGGGAAAGATTAGG[A/C]ATCTTAATTTTTGCT	100507650
rs759200375	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23255528	TTATCCAGACAATGT[G/T]AAGTGTTATCATCAA	100507650
rs759220124	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218896	CCTCCGGGCATTTAA[C/T]AATCAAACTCCCAAA	100507650
rs759223605	in-del	-/TTTG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208763	TGGTTGCCGTTTTTT[-/TTTG]TTTTTTTTTTTTTGA	100507650
rs759243753	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221056	CAAAAGTGGCTGAAT[A/G]GATGAAAAAAAGACA	100507650
rs759277522	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23188858	ACCTAAAATGGTGCC[-/T]TGGCACTCAATAAAT	100507650
rs759285044	in-del	-/GAA			intron-variant	RNF212B	GRCh38.p7	14:23238769	TAATAATAATAATAA[-/GAA]TAATAATAATAATCC	100507650
rs759286170	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23243977	CAGCTACTCAGGAGG[C/T]TGAGGCAGAAGAATC	100507650
rs759451186	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23228555	CAGGGAGGATGAGCA[A/G]GGAGGATCACTTGAG	100507650
rs759469709	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23217533	CATGGGTGCTTGCAT[C/T]GCCACACCCACAGCT	100507650
rs759493620	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23227361	TATTAGAAAGCAGGA[C/T]AATGGTTGCCTTTAG	100507650
rs759580080	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23258997	ATCAGCCTGGGCAAC[-/T]ACAGCGAGACTCTGT	100507650
rs759628081	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204174	CCCACTCTGTGGGTT[A/G]TCTGTTTACTCTGCT	100507650
rs759640305	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23264600	ATATATTTATTAATT[C/G]ATGCTTATTATTTGT	100507650
rs759681178	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209778	CAACTCAAAATTAAT[A/G]TCATCAGTTAGATAT	100507650
rs759683439	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23226424	TCACCAGGTCAGGAG[A/T]TCGAGACCATCCTGG	100507650
rs759714149	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206004	ATATTTCTAATAGTA[C/T]TTTACCAGTAATTTT	100507650
rs759715163	in-del	-/ATATATATATATATATA			intron-variant	RNF212B	GRCh38.p7	14:23229224	TGAATAATATTTTAT[-/ATATATATATATATATA]TATATATATATATAT	100507650
rs759715931	snp	A/C	0.000242277	0.0110036	missense, synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269907	TTTTTTCTTTCAGAC[A/C]ATCCCCAAATGGGCA	100507650
rs759775121	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23252043	GAATTTGTCATTGGC[A/G]ATTGAACTCAATCTC	100507650
rs759788600	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23223246	ATGTCACTTCATGAC[-/A]AAAAAAACCCTTAAA	100507650
rs759880029	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206969	AACAAACAAAAACAT[G/T]AAGGCCTTTCAAATA	100507650
rs759900590	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23193438	AAAGAGAATTCCTAG[A/G]ATAAGAGGGTGAATT	100507650
rs759913801	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213015	AAAAGACCTGTACAC[C/T]AAAAATTATAACACA	100507650
rs759913935	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23223878	TTAGAATTGATTTTT[A/T]AAAATCCAGTAAAGT	100507650
rs759920401	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23246872	TTGGCCGGGTGTGGT[A/G]GCTCACGCCTGTAAT	100507650
rs759952671	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23226291	GACAGAGCAAGAAAC[A/C]GTCTCAAAAAAAAAA	100507650
rs759958431	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23258211	GGCGTGGTAGCACAT[A/G]CCTGTAAACCCAGCT	100507650
rs759972174	in-del	-/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259363	TGGCTAATTTTTGTA[-/T]TTTTTTTTTTTTTTT	100507650
rs759997179	snp	C/T			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199487	TTCCCTTTAGCTTAG[C/T]GATTTGGGGGCCCCA	100507650
rs760073160	snp	C/T			intron-variant, splice-donor-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213997	AATGAATTGGGTGTA[C/T]CTGTAGTCCTAGCTG	100507650
rs760102526	snp	C/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260043	TAATCTTTTTCTCAT[C/G]ATGGCACACACAGAA	100507650
rs760131363	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23247057	AGGCAGGAGAATCAC[C/T]TGAACCTGGGAGGTG	100507650
rs760177212	in-del	-/CTT			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215835	TAAATGTTGACTATC[-/CTT]CTCCTAGTCCTTATC	100507650
rs760224374	in-del	-/TT			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203483	TACTTTTAGTCCCCC[-/TT]TTTTTTTTTTTTGAG	100507650
rs760252814	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23253532	CATTGGTTTGGGGGC[A/G]GGGAAAGGTGAGGCA	100507650
rs760270162	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23273127	TCTTCCAGAAGACAC[C/T]GGTAGCTCCCCTCAT	100507650
rs760310236	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23266834	TATAGAGTCTGCTAG[A/G]TTTAGCTAGTATATC	100507650
rs760310264	snp	A/G	0.000497389	0.0157622	missense, utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23244342	GCCTCAGGAGAAGAT[A/G]TTTTTCAAAAGTCCT	100507650
rs760353487	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23219103	GTGAAATATCCTTCA[A/G]ACATGAAGGAGAAAT	100507650
rs760380849	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23233969	AGGCCTGGTGGTGTG[G/T]GCCTGTAGTTCCAGC	100507650
rs760389527	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209430	AGTTGCTCTGGTTCA[C/T]ACACCTCTGACAGTA	100507650
rs760469969	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195661	GTGCTCTCCCGACAG[C/T]ACATCCACCCTCCTA	100507650
rs760612839	in-del	-/AAAC			intron-variant	RNF212B	GRCh38.p7	14:23254288	TACTCTTTATCTCAA[-/AAAC]AAACAAAACAAAACA	100507650
rs760638175	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23224124	GATATTTCATGTTCA[C/T]GGATTGGAAGAATCA	100507650
rs760651520	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196552	TCAAGCAATCCTCCC[A/G]CCTCAGCCTCCTGAG	100507650
rs760715321	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23261825	ACAAAATTAGCCGGG[C/T]GTGGTGGAGGACACC	100507650
rs760719296	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23225374	TGTGTGTTGCAGCAC[C/T]GTTCACAATAGCCAA	100507650
rs760737935	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23268801	CACTTGGCATTAGCC[A/C]CCAACCCTAACCCAT	100507650
rs760769273	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215278	GAGTCCTCCCTAGCC[A/G]TGCAGAACTGTGAGT	100507650
rs760793014	snp	A/G	0.000242512	0.011009	missense, synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269939	TCAGGCCACACAAGA[A/G]TCCTCACCCCCAACA	100507650
rs760949803	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23263128	AACTGTATCCAGCTT[G/T]ATTAAAGATACTGTC	100507650
rs760979747	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23193198	AATGTCTTCAAAATT[C/G]AGAAGGAATATGATT	100507650
rs761015088	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204036	CTCTTGAGAATTGTC[G/T]ATTCATGTCCTTAGC	100507650
rs761043294	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23229572	ATTTAGAAAATTCTA[G/T]CCACCCCACCACATG	100507650
rs761054172	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23258694	AAGTCCCAAGAGAGC[-/T]TTTTTTTTTTTTTTT	100507650
rs761146232	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23238653	TGAGGTGGGAAGATC[C/G]CTTGAGCCCAGGAGT	100507650
rs761162048	in-del	-/AAC			intron-variant	RNF212B	GRCh38.p7	14:23254295	TTATCTCAAAAACAA[-/AAC]AAAACAAAACAAAAC	100507650
rs761227119	in-del	-/AA			intron-variant	RNF212B	GRCh38.p7	14:23243695	GTAAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA	100507650
rs761234172	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23222910	ATACAAAAAATTAGC[C/T]GGGCATGGTGGCACG	100507650
rs761247850	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23271016	TACTACTTGAACTAG[A/G]AAAAACCACATTTAC	100507650
rs761345508	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23246863	AAAAAATTGTTGGCC[A/G]GGTGTGGTGGCTCAC	100507650
rs761354448	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23258122	GGTGGGTAGATCACC[C/T]GAGGTCGGAAGTTCA	100507650
rs761419065	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200412	CCCACTGCAACCTCT[A/G]CCTCCTGGGATCAAG	100507650
rs761427295	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229791	AGTTCTCACATATTT[A/G]TTACTGAACCCAGAC	100507650
rs761438365	snp	A/C			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199116	GACAGGTCTCAGTTA[A/C]TTGTTTATTTTGCCA	100507650
rs761462129	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23242108	AAAAAAAAAAAAAAA[-/G]AAAAGAAAAAGAAAA	100507650
rs761463511	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23257432	ATCTAAAACTAGTTT[A/C]GTTTACTTTCAAGTA	100507650
rs761469188	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23235511	TTCTCAAAAATAAAC[-/A]AAACTGCCTTGCCAC	100507650
rs761498390	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23228728	GACTACATCATTTCA[A/G]GACTTATCATAAGGC	100507650
rs761508387	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260856	AAAATCTTAATTGTA[A/G]TGCTCACCCTGGATT	100507650
rs761614201	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205942	GGGTAAGTATGAAAT[C/T]TGCTTGATTAATAAT	100507650
rs761617749	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23186743	CTCATGTAGTATCTT[A/G]GGCAGACGAGGCAGT	100507650
rs761664576	in-del	-/GGCAGTGGTGG			intron-variant	RNF212B	GRCh38.p7	14:23217247	AGTGGTGGCAGTGGT[-/GGCAGTGGTGG]GGGGGGGGCTCCTCT	100507650
rs761777660	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208143	TTTATTTCCTTTCAC[A/C]ATAAGGGCAACCTGG	100507650
rs761783082	in-del	-/AAA			intron-variant	RNF212B	GRCh38.p7	14:23233742	GTGAGACCCTGTCTC[-/AAA]AAAAAAAAAAAAAAA	100507650
rs761802838	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23253410	CTTTTGTCTATAGAG[C/T]TGTTCACAGTGTGGA	100507650
rs761836012	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273924	TTTACAGTTTTTGTT[C/T]TTTTAATTTACCTCA	100507650
rs761857335	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23240303	AGCTATAATTATGTT[A/T]TTCTCTAGGTTATTC	100507650
rs761893241	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213770	GTAGAGAGAGAGAAA[A/G]AGAGGCAGAGAGAGA	100507650
rs761931952	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23241935	AAACTACAAAAAATT[A/T]GCCGGGCATGGTGGC	100507650
rs761940006	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23192642	TATACATATGTAACA[A/G]ACCTGCACTTTGTGC	100507650
rs761948872	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23224142	ATTGGAAGAATCAAC[A/G]TTGTTAAAATGTCCA	100507650
rs762025270	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23248337	TACAGGGTTTTACCA[A/T]GTTGCCCAGGTCTCG	100507650
rs762102779	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23238779	AATAATAATAATAAT[-/C]AATCCCACAAAGAAA	100507650
rs762108378	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23225152	TTCAAAAGTCAGGCA[A/G]TAACAAGTGCTGGCG	100507650
rs762116070	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203770	GGCATGAGCCACCAT[A/G]GTAGGCCTTACTTTA	100507650
rs762180522	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202581	TTTAGGCTGGGCGTG[A/G]TGGCTCACGCCTGTA	100507650
rs762270311	snp	A/G	0.000123693	0.0078633	intron-variant	RNF212B	GRCh38.p7	14:23262633	CCTCTGCCTAGAGAG[A/G]TTAGAGCCGCCTCTT	100507650
rs762279875	snp	C/G	0.000125133	0.00790891	missense, utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23258570	AGTTTCCAGAAGAAA[C/G]AAACAGATCTCCTCA	100507650
rs762289735	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221129	CAGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT	100507650
rs762366567	in-del	-/TTA			intron-variant	RNF212B	GRCh38.p7	14:23267301	TATTGTCAAATTGTC[-/TTA]TTTTCTCTTCAATTC	100507650
rs762385519	in-del	-/CTT			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236961	TTATTCTGTCTCTCT[-/CTT]TTTTTTTTTTTTTTG	100507650
rs762439751	snp	C/T			missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23268936	CAGAAACCCCTTCAC[C/T]GGCTTCAACTCATAG	100507650
rs762444401	snp	A/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237498	ATTAATATCACACTG[A/T]TCTTTGTCCGCATCA	100507650
rs762458143	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201431	ATTATTGTTATTGAT[A/C]ATGTACACTAAGTTA	100507650
rs762528842	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23245314	TGCTTGGTTGAGCCA[C/T]CATATTTGACATACA	100507650
rs762572978	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23255837	TAATTTTTTAAAGTA[C/T]TGTACTGAGGTACAT	100507650
rs762576232	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210983	AATTCACTTTGGGAG[C/G]CCAAGGTGGACAGAT	100507650
rs762600538	snp	C/T			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270488	TTGCTGATTGTGTTT[C/T]CCTTCTGAGTAGTGT	100507650
rs762632992	snp	C/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184929	ATTAAATATATTATG[C/T]AAAATTATTTAATTT	100507650
rs762649079	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202195	GGAGGAGCTTGCAGT[A/G]AGCCGAGATTGCGCA	100507650
rs762663055	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23244011	TGAACCCAAAAGGCG[A/C]GGGTTGCAATGAGCC	100507650
rs762707416	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23221165	GCTGAGGTGGACAGA[A/T]CACTTGAGGTCAGGA	100507650
rs762763748	in-del	-/C	0.000463795	0.0152211	intron-variant	RNF212B	GRCh38.p7	14:23243318	ATAATGTAAGTTTTT[-/C]CTCCCCCTGCCACAA	100507650
rs762826470	in-del	-/ACA			intron-variant	RNF212B	GRCh38.p7	14:23225080	TTGATGCCACCCCAC[-/ACA]AAAAAAAAACACCTA	100507650
rs762828402	snp	G/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199001	GCTATACCTCACGCT[G/T]TCCACTGAGAGGGCC	100507650
rs762839154	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23186538	TGTTTTTAGTAGAGA[C/T]GGGGTTTCACCCTGT	100507650
rs762884894	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207039	ATCCTTTTAATTAAG[C/T]TGATTTTTAACCATT	100507650
rs762945149	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23218757	AGGTAGAGAAAGAGA[A/G]CTAGGGGTAGAAAGT	100507650
rs762958252	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212223	TATGATCAAGACTAA[A/C]ACAAGGATGTCTGCC	100507650
rs762988875	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23252133	CCCCAACCCTCTAAA[C/T]AGTGTTTGGTTCCCC	100507650
rs763017114	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206135	GCTGGAGTGCAGTGG[C/T]AGGATCTCATCTCAC	100507650
rs763020430	in-del	-/AAAA			intron-variant	RNF212B	GRCh38.p7	14:23254287	AATACTCTTTATCTC[-/AAAA]ACAAAACAAAACAAA	100507650
rs763035898	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23190085	GCTAATGGCTCTGGA[G/T]CACCCACTCTCCTGG	100507650
rs763046768	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23226714	TCTTCGTGGTGCTGG[A/G]CCAGTCTCGTCTTAT	100507650
rs763076763	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23253289	CACATTTTGAATTGA[A/G]TTTCAATAAAGGTAT	100507650
rs763086798	in-del	-/TCTACCT			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213688	TTAGGAACTGTGTGC[-/TCTACCT]AAACAGGGTGACTGC	100507650
rs763131868	snp	C/T	0.000121884	0.00780559	missense, utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23258589	CAGATCTCCTCATCG[C/T]CTTTTATAAGCATAG	100507650
rs763170149	snp	A/C			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273754	AGGCATTTCTAGATA[A/C]CTTCTCTTTTAGGCA	100507650
rs763179664	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260416	CTCACCAGAGACTCC[A/G]TATTTCCCCACATAT	100507650
rs763237965	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23225079	TTGATGCCACCCCAC[-/A]ACAAAAAAAAAACAC	100507650
rs763243831	snp	A/C			missense, utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23258560	GTAGGTGTGGAGTTT[A/C]CAGAAGAAACAAACA	100507650
rs763250367	snp	A/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215091	CTGGTGGGAGGTGAT[A/T]GGATCATGCGGGCAG	100507650
rs763314616	snp	C/G			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23214046	GAGGATCACTTGAGC[C/G]CAGGAGTTCGAGGTT	100507650
rs763332609	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200953	TAGTTTTCAAATTCT[A/G]GAGAAAATCAATTAC	100507650
rs763343265	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23224717	TCTTGTGTAATACCC[A/C]ACAAGCTCAGGCAAC	100507650
rs763383617	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23272729	AAAGCAGTGGTGTCT[A/G]TCTCGATAAGCTTCA	100507650
rs763433586	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23187995	GAAGATGAAATGAGG[A/G]GACTCGGTCAGTGAT	100507650
rs763509977	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218321	TGCAGTGAGCCAAGA[C/T]TGCACCTCTGCACTA	100507650
rs763572339	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23244036	TGAGCCTAGATCACA[C/G]CACTGCACTCCAGCC	100507650
rs763670647	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23227478	TGTGTTGAGTTTGTG[A/G]AAATTCAGTAAGCTA	100507650
rs763744678	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23231788	GCGATTGCAGGCACG[C/T]GCCGCCACGCCTGAC	100507650
rs763746906	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196959	TTAATGTCTACCTCC[C/T]CATCTAGACTGCAAA	100507650
rs763762590	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23228649	GCAAGACTCTCTAAA[A/G]AAACAAAAAAACAAA	100507650
rs763762683	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23216697	CAAGCTTGGGCAACA[C/T]GGTGAAACCCCATCT	100507650
rs763833163	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229949	TATGTGTGCCATCTC[A/G]TGCACAATTCCTTAT	100507650
rs763833250	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23255174	CACTTTTTGTTCTCT[G/T]TTTCTGCTTTCTTCA	100507650
rs763878840	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202252	CAAGACCCTGTCTTA[-/A]AAAAAAAAAAAAAAA	100507650
rs763913796	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202520	ATTTTATTTTGATTG[A/G]CATCTTCTACAGGGC	100507650
rs763925815	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206202	GCCTCAGCCTCCCCA[A/G]TAGCTGGGATTATAG	100507650
rs763985396	in-del	-/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204709	TGGCTATGCAGGCAC[-/T]TTTTTTCATTCCATA	100507650
rs764031954	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23262122	TTCTTTTGTCCTTCT[A/G]TACTTCTGATAAGCC	100507650
rs764082528	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23252184	GATGCTACCTAGGAC[C/T]CACCAAGAGTCACCT	100507650
rs764098160	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207052	AGCTGATTTTTAACC[A/G]TTGAGCTGCTTAAAA	100507650
rs764165201	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23224029	GAGGAATTAACCAAA[G/T]AAGTAAAAGATCTCT	100507650
rs764181145	in-del	-/GTCT			intron-variant	RNF212B	GRCh38.p7	14:23226763	CTCCCCTCCCCTCCC[-/GTCT]CCTCTCCTCTCTTCT	100507650
rs764185149	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23238385	CAGTACATTTTTTAT[C/G]GTAAATCTTACGAAG	100507650
rs764230589	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210415	AAAATGAGATTTGAA[A/C]AAAGTCTGGAGTTTA	100507650
rs764247947	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23239232	CCAGCTAATTTTCTT[C/T]TATTTTTAGTAGAGA	100507650
rs764249545	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273807	GAGTTACCTCCAAGA[C/T]TGTTGTATCTCTGTT	100507650
rs764343138	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23247316	AGTGGTTTTTAATAC[A/C]TCCACAGAATTGTGC	100507650
rs764344939	in-del	-/T	0.0333238	0.124705	intron-variant	RNF212B	GRCh38.p7	14:23258693	AAGTCCCAAGAGAGC[-/T]TTTTTTTTTTTTTTT	100507650
rs764367355	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212269	CAACATTATGCCGAT[A/G]GCTATGGCCACTGCA	100507650
rs764496549	in-del	-/C			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23194746	CTCAAAAAAAAAAAA[-/C]AAAAAAAAAAACAAC	100507650
rs764552144	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23188002	AAATGAGGAGACTCG[C/G]TCAGTGATTAAGCCC	100507650
rs764582567	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202545	CAGGGCCTAAAGATG[A/G]GGCTTTAATTGCTGT	100507650
rs764595974	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23234367	ATTTGTCAATATTTT[C/T]TCTCTTCTAGATTTT	100507650
rs764600634	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23227259	AGTAGAAACTTTATT[C/T]GTTGATCAGGGAATG	100507650
rs764604717	in-del	-/GAGT			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260815	CACTTCTCCGAGGAA[-/GAGT]TAGTTACTGAAAGTG	100507650
rs764605355	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23189405	CTCCCAAAGTCTCAA[C/G]ACTTTGCTCTTGAAA	100507650
rs764612663	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23266963	ATTATTGTGGTTTTT[C/G]GTTTTTTGTTTTCTT	100507650
rs764622975	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23267774	CTGATATTAGTATAG[A/C]CACTCTTTTGTTCCT	100507650
rs764640268	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197665	ACATTCCCCAAAGGA[A/G]AGAGAATAATACAAT	100507650
rs764712490	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23254359	TAAAACTAAAACTGG[A/G]CATGGTGGCTCACTC	100507650
rs764782651	in-del	-/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203484	ACTTTTAGTCCCCCT[-/T]TTTTTTTTTTTTGAG	100507650
rs764785827	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209089	TGGTTATGTATTGAT[A/G]ATATGCTAAACAAGG	100507650
rs764803369	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23242392	AGGAATCTTAATTTT[C/T]GCTTCTTTCAGATTG	100507650
rs764881502	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221060	AGTGGCTGAATGGAT[A/G]AAAAAAAGACACAAT	100507650
rs764891468	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23243994	GAGGCAGAAGAATCA[A/C]TTGAACCCAAAAGGC	100507650
rs764958014	in-del	-/TG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206787	AATTAAACTATACTC[-/TG]TCTTAAAAACCCAAG	100507650
rs764962656	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23225549	GTTAAGTGAAAAAAG[C/T]CAGGCACAGAAAGAC	100507650
rs765022173	snp	A/C			utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183625	CACAGCCGGCCCCAT[A/C]CCTCTGGTTTCGGGA	100507650
rs765115021	in-del	-/GT			intron-variant	RNF212B	GRCh38.p7	14:23234299	TGCTTTACTTTTCGT[-/GT]GTGTGTGTGTGTGTG	100507650
rs765120661	snp	A/G			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274734	AACATGATGAAACCC[A/G]TCTCTACTAAAAATA	100507650
rs765121976	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204276	TATATTTGCTTTTGG[A/G]TTCTTGGTCATGAAA	100507650
rs765122554	snp	A/G	0.000121603	0.00779657	missense, synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269951	AGAGTCCTCACCCCC[A/G]ACAATTTTGGTAAGT	100507650
rs765151785	snp	G/T			utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23238028	TTCCTGAGATCTGAG[G/T]CTTTCTGGAATCACA	100507650
rs765196276	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23188867	TGGTGCCTGGCACTC[A/C]ATAAATATGATTGAT	100507650
rs765227148	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23263496	AATCAATGACTGGGG[A/G]TCAGGTCCTAACAGA	100507650
rs765277284	snp	C/T	0.00012351	0.00785747	intron-variant	RNF212B	GRCh38.p7	14:23240486	TCAGGGAAAAATGTT[C/T]TCATGTAAGGATGTA	100507650
rs765318276	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23239103	GAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	100507650
rs765339031	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23250667	CAAGTCTCAGTTAAT[A/T]TAGAAAGTTTATTTT	100507650
rs765410333	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206059	TTTACTTATTACATA[A/C]ACCTGAAAAAGCATT	100507650
rs765443416	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210001	CTGTTAAAAATACAA[A/C]AATTAGCTGGCATGA	100507650
rs765461682	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23190824	AACCTGGAGGTCCTG[C/G]TGGCCACTTGGACTT	100507650
rs765467464	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23247053	GCTGAGGCAGGAGAA[C/T]CACTTGAACCTGGGA	100507650
rs765481079	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23252091	CTGATTGTCAGGGGT[A/T]GGGGGGCGTGGGAAG	100507650
rs765490688	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23257702	ATCCCATGATAGACA[C/T]ATTAGTATAGCAAAT	100507650
rs765540205	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208993	TCGATCTCCTGACCT[C/G]GTGATCCGCCCGCCT	100507650
rs765713626	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193624	AAGAAGAACTAGCGA[C/T]AGTGACACAGAAAAG	100507650
rs765890933	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266858	GTATATCGTGTTGTT[C/T]AATTAGTATGCTTCT	100507650
rs765954921	snp	C/G			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237843	TCTGCGGGCCCCGCC[C/G]ACGCCCCGCGCACGC	100507650
rs765984031	in-del	-/AAT			intron-variant	RNF212B	GRCh38.p7	14:23238741	ACCCTGTCTCAAAAT[-/AAT]AATAATAATAATAAT	100507650
rs766055822	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208257	CCGGATGTGGTGGCT[A/C]ACACTTGTAATTCCA	100507650
rs766060314	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23216999	GATTAGTGACTGACA[A/G]ATGTTAAGAATGGGG	100507650
rs766107808	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195778	GTGCCAGACACTTCA[C/T]GTAACAAGGAATTTC	100507650
rs766151883	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236159	ACAAAAATGTAAAAA[C/T]GATGCCACTCTTCTC	100507650
rs766167471	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23225403	AAGATTTGGAAGCAA[A/C]TTAAGTGTCCATCAA	100507650
rs766170803	snp	G/T			missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240400	GGGGCCCATTTCTTT[G/T]TCACCAGCTGTGGCC	100507650
rs766257699	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208707	GAAAGTAAAGGAATA[A/G]AAGAATGGCTACTTC	100507650
rs766269338	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196702	CTGCCTAGGCCTCCT[A/G]AAGTGCTGGGATTAC	100507650
rs766280658	snp	C/T			utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274129	TTTAGATGGTTAACT[C/T]ATTGATGATACCTAT	100507650
rs766322761	snp	A/T			utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183482	CGGTGTTGCTCTAGA[A/T]CTGGTTTCCACCTGC	100507650
rs766363800	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23256800	CAAGCAATCCACCCA[C/T]TTCAGCCTTTCAGGT	100507650
rs766454987	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23261826	CAAAATTAGCCGGGC[A/G]TGGTGGAGGACACCT	100507650
rs766510835	snp	A/G	0.000122692	0.0078314	missense, nc-transcript-variant	RNF212B	GRCh38.p7	14:23258631	TAGAAACAGCCATGC[A/G]GGAGGCACAGCAAGC	100507650
rs766517515	snp	A/G			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236134	CTATTAAGCTACATA[A/G]CAAGAGATTACAAAA	100507650
rs766607550	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237727	TACAGTGTTTATTTG[C/T]CCCCAATCTTTTAAG	100507650
rs766609739	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23265251	AGTAAAATTGACTTG[A/G]ATTTTTTTGAATTGC	100507650
rs766612860	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23223151	TGCAAATCAATATAC[A/G]TCGTACATCATATCA	100507650
rs766613141	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203052	AGTTCTTTAGTGGTG[A/G]TTTGTGAGATTTTGG	100507650
rs766631294	snp	A/C	0.000120489	0.0077608	intron-variant	RNF212B	GRCh38.p7	14:23262727	GTGGAGAACATTTTT[A/C]CCCTAAATATCTGTG	100507650
rs766641187	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23269169	ATTAGCCGGGAGCGG[C/T]GTCACGTGCCTGTAA	100507650
rs766702702	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204055	CATGTCCTTAGCCCA[C/T]TTTTTGATGGGATTG	100507650
rs766725398	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23243025	AGGGAGATGGGTAGA[C/T]GTACGGTGTGAAAGC	100507650
rs766770671	snp	A/C			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215235	GCCTTGCTTCTCCTT[A/C]ATTTTTTGCCATGAT	100507650
rs766840612	in-del	-/AC			intron-variant	RNF212B	GRCh38.p7	14:23239994	AAAAAGTAAAGGAAA[-/AC]ACACACACACACACA	100507650
rs766861293	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23256112	TGTTTATGCACTTAC[A/G]ACCCTTGGTAATGTC	100507650
rs766886665	snp	A/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199249	GACATCAATCAATAT[A/T]TGTAAGAAGTACATT	100507650
rs766949142	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23257577	AAAAGAGGGTTTATA[A/G]TCTGAACAGGGAGGA	100507650
rs767005499	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23228765	AAGTGACAGTATGGT[A/G]TTGGCATCAAGACAG	100507650
rs767021825	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23217980	AGGAACTCAAAAAAA[C/T]TCAAGATAATGCAGA	100507650
rs767026548	in-del	-/TG			utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183456	TCTAGAAAAACAAAC[-/TG]TGAACCTGACGGTGT	100507650
rs767091242	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23257510	TTTGAAAATTAAGTG[A/G]GAACAAAAAGTTTAT	100507650
rs767130735	snp	C/T	0.000121426	0.00779089	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240356	CCAGAATGGATTGGT[C/T]TCATTGCAACCAGTG	100507650
rs767137709	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23229802	ATTTATTACTGAACC[C/T]AGACTACTAGCGCAC	100507650
rs767145841	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23264979	GGCATGTGCCACCAC[A/G]CCTGGCTAATTCTGT	100507650
rs767150010	in-del	-/AACA			intron-variant	RNF212B	GRCh38.p7	14:23272430	CTCAAAAAAACAACA[-/AACA]AACAAACAAACAAAC	100507650
rs767179783	in-del	-/A			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184098	ATCTTCGAGTTTCCT[-/A]AAAATAGGGGGAATC	100507650
rs767265725	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266789	TATGTGGAAAGAATG[C/T]ATATTCTACTCTTTT	100507650
rs767276464	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23186751	GTATCTTGGGCAGAC[A/G]AGGCAGTTATCTTAA	100507650
rs767309699	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23252280	CTCAGGAAATGCCAA[A/C]GGTTTTAGTAACTCT	100507650
rs767329639	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23187721	CAGTCCATGCGCTCA[C/G]TCCATCCTTCTTCTC	100507650
rs767365094	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23221605	TAGAAAATCAACAAA[C/G]ATCAGACTTAATCTG	100507650
rs767370184	snp	C/G			missense, nc-transcript-variant	RNF212B	GRCh38.p7	14:23262943	TTACCCCACGACCCA[C/G]TTTCCAGCATAGCAG	100507650
rs767402156	snp	C/G			utr-variant-3-prime, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272935	CTGCTGAAGGATGGA[C/G]TGTAGCTTCCAGTAC	100507650
rs767426507	snp	C/T	0.000363482	0.0134762	missense, synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269910	TTTCTTTCAGACCAT[C/T]CCCAAATGGGCATTC	100507650
rs767437033	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208156	ACAATAAGGGCAACC[C/T]GGGCTCCTTGGAGAA	100507650
rs767479374	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23223080	AAAAAAAGGAAAAGA[A/T]AAGATTGTTCATCAT	100507650
rs767584366	in-del	-/G			intron-variant	RNF212B	GRCh38.p7	14:23220802	TGCACTCCAGCCTGG[-/G]AGACAGAGCAAGACT	100507650
rs767585487	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23220458	AATTATTGGAACCCA[A/G]GAGATGGAGGTTGCT	100507650
rs767588846	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23224165	AATGTCCATGCTACC[C/T]AAAGTAATCTACAGA	100507650
rs767626337	snp	A/G			utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274051	AGTGGTTGAGAGAGA[A/G]ACAATTTTATTTTTG	100507650
rs767665663	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23189212	TGACATCTTTGACTA[-/T]TGTTTCATGGAGAAA	100507650
rs767753758	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23234904	AACACAGTGAGACCT[A/T]GTCTCTTAAAAAAAT	100507650
rs767767171	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201249	CACTCAAGAGCACCT[C/G]TTATAGTTTAATAGC	100507650
rs767802200	snp	A/G	0.00108926	0.0233119	missense, nc-transcript-variant	RNF212B	GRCh38.p7	14:23262937	TTTCAGTTACCCCAC[A/G]ACCCAGTTTCCAGCA	100507650
rs767818115	in-del	-/AAT			intron-variant	RNF212B	GRCh38.p7	14:23218377	TATCTCAAAAAAAAA[-/AAT]AAATAAAAAGAAGAA	100507650
rs767842621	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23249285	CTCAGTGGGCCAGGC[A/G]CAGTGGTTCATACCA	100507650
rs767901995	in-del	-/AAAAAAAAAA			intron-variant	RNF212B	GRCh38.p7	14:23193092	AGAAAAACTCTGTCT[-/AAAAAAAAAA]AAAAAAAAAAAAAAA	100507650
rs767927209	in-del	-/TGATACCTT			intron-variant	RNF212B	GRCh38.p7	14:23240854	TAGAAATGATGATGA[-/TGATACCTT]TGCAGCTTAAAAAGC	100507650
rs767943980	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23221918	GATATTAAGAAGGAA[A/T]CTGAAAAGTGCCTTG	100507650
rs767994669	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23235819	ATGATGTTACAAAAT[C/T]GTGCATGGGCAAAAG	100507650
rs767996341	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23268042	TTTGTCCCAGCTGAT[A/G]TTTATCTCCTTAGGC	100507650
rs768019320	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23254582	TGCTTTTGGTAGAGA[C/T]AGCATTTTGCCACGT	100507650
rs768031855	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23185798	ATTGATTACTGGTGC[A/G]ATGTAATATCTAGGA	100507650
rs768088170	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23269052	GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG	100507650
rs768170004	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210023	CTGGCATGATGTGTG[A/T]GCCTGTAATCCCAGC	100507650
rs768174705	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23194145	CCATTCCTGGCCTCA[C/T]ATACTATCACTTAAA	100507650
rs768185432	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23223659	CGCGCCCGGCCAAGC[C/G]TTTCTTTTCAGATCT	100507650
rs768335682	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272112	GAGTTCATTATACTA[C/T]TCTATGTATTTTTTG	100507650
rs768569464	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208063	AGAGAATGGGAGGCA[C/G]GTTTGCCCTAAGCAG	100507650
rs768592089	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267170	ATGTCTTTGTAGAGA[C/T]GAGGTCTCCCTGTTC	100507650
rs768634666	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23241710	ATTACAGGTGTAAGC[C/T]ATTTTTTTGTTTTGT	100507650
rs768651006	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23264488	AAGGAGTAAAGTATG[A/G]ATCTTTCTTTGACTA	100507650
rs768703122	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23187644	TTCTTGCTTTTTGTA[A/G]CAGAGCTGGGAAGTC	100507650
rs768747667	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23228626	CGCAATCCAGCCTGG[A/G]TGACAGAGCAAGACT	100507650
rs768768709	in-del	-/ACTCGGGA			intron-variant	RNF212B	GRCh38.p7	14:23230542	CCTGTAGTCCCAGCT[-/ACTCGGGA]ACTCGGGAAGCTGAG	100507650
rs768834065	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209283	TTACCGCAACCTGTT[C/T]TACCAGCAAGGTCTT	100507650
rs768976345	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23248972	TGCTGTTGTAGCATG[G/T]AAGCAGCCATAGACA	100507650
rs768979866	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196164	CTCTGCAAATCAGAG[C/G]CTAGACACTTAGCCA	100507650
rs769076689	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23239100	ATGGAGTCTCACTCT[G/T]TCGCCCAGGCTGGAG	100507650
rs769083704	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23262800	CAGAGACAATAATGT[A/G]ATCTTCCTAACTTTA	100507650
rs769121862	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204304	AAATCCTTGCCTAAG[C/T]CAATGTCTAGAAGCA	100507650
rs769165587	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203583	TTCCGGGTTCAAGCA[A/T]TTCTCATGCCTCAGC	100507650
rs769227022	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23250088	ACGTAAGGTTATTTA[C/T]TACCTAATCTATTAG	100507650
rs769228494	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23219526	GCGCAGACTGGAGTG[C/T]AGTGGCAAGATCTCG	100507650
rs769289117	snp	C/T			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270258	AAAATGCTGGGCGCT[C/T]AGTTCTGAGGATTAT	100507650
rs769378106	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23244106	AAAGTATAAACAACA[A/G]ATGGAAGCATTATTT	100507650
rs769388493	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237463	GTTGACTTTTTTTAA[C/T]TGAAATTTGTTAGTT	100507650
rs769406915	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23268742	CATGAAAGGGAGAGG[A/G]AAGCACCTATAAGAG	100507650
rs769415236	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23228653	ACTCTCTAAAAAAAC[-/A]AAAAAAACAAAACAA	100507650
rs769454396	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23257209	TTTCATAGAGACAGG[A/G]TCTTGCTATGTTGCT	100507650
rs769465846	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23241459	GACATAGTCTCACTT[C/T]GTCACCCAGGCTGGA	100507650
rs769561775	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23221841	ACAGGAGGAATTTTG[A/G]AAAGTATATGAACAC	100507650
rs769663079	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23246500	TCATACTTCCTCACA[G/T]GTAATATGAAATAAT	100507650
rs769663135	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23228579	ACTTGAGCCCAGGAC[A/T]TCCAGGTTGCAGTGA	100507650
rs769666847	in-del	-/CA	0.00024216	0.011001	intron-variant	RNF212B	GRCh38.p7	14:23262881	GCCAGGCAAGGCAGG[-/CA]TACCATTGATGGCAA	100507650
rs769692724	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23191693	GTTTATATTGTTTAA[A/G]TGGGATGATGGGTAA	100507650
rs769721327	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23187417	GTAGTGGCACAATCA[A/C]AGCTCACAGCAGCCT	100507650
rs769781864	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23189987	GTCACCAACATCTAC[G/T]CTATCAGTTGGACCA	100507650
rs769783492	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214617	AAACTTCATTGGATA[A/G]GATCAATAACAGAAT	100507650
rs769799848	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213498	CATGAGGCGGAAAGA[A/G]GAAGTATTGAGACAA	100507650
rs769817535	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218573	ATGATCACACCACTG[C/T]ACCCTAGCCTGGGTG	100507650
rs769871549	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211954	GCTGGTCTTGAAGTC[C/T]TGACCTCAAGTTATC	100507650
rs769973888	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23264618	GCTTATTATTTGTCT[A/G]TCAGGGAGGCAGAGG	100507650
rs769981137	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23251238	TCTCTGACACCAACT[-/A]AGGTATGCAACAATT	100507650
rs769987550	snp	A/G	0.000123862	0.00786865	intron-variant	RNF212B	GRCh38.p7	14:23262642	AGAGAGATTAGAGCC[A/G]CCTCTTTTTTTTTCC	100507650
rs770051814	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23219379	AACAACAGCTTTTTA[A/G]GACAAAGACAGTGCA	100507650
rs770067022	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266029	TTGCCCAGACTGGAG[C/T]GCAGTGGTGCCATCT	100507650
rs770074862	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23253085	TTGCCACCCCCACCC[A/C]GATTATTTTAAAGCC	100507650
rs770078445	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23239876	CACCTGCCTCGGCCT[C/G]CCAAAGTGCTGGGAT	100507650
rs770096476	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23241082	AAGGTGTGTAAATCC[C/T]TAGAAGAGGGACTTG	100507650
rs770140087	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23262998	AGCAACATTAAAACT[G/T]TTGGCAAAAGTTGGA	100507650
rs770188587	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23224860	AACTTTCCATCTGAC[A/G]AGGGATTAATAACTA	100507650
rs770236108	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23223945	TTTTTATATGCCAAC[A/G]GTGAATAATCTGAAA	100507650
rs770286840	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23232413	TCCGCCCGGCAGCCG[A/C]CCTGTCTGAGAAGTG	100507650
rs770358447	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23261488	TTTTTACACTACTCA[C/T]CCTTCAAAATTGAAC	100507650
rs770382140	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202046	GCTTGAGGTCCGGAG[C/T]TCGAGACCAGCTTGA	100507650
rs770384884	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23241260	TCACAAAACCATAGT[A/G]CAGGGGACTACACAT	100507650
rs770403186	snp	G/T	0.000246914	0.0111084	intron-variant	RNF212B	GRCh38.p7	14:23240316	TTATTCTCTAGGTTA[G/T]TCTTACTCTTTCTCT	100507650
rs770412477	snp	A/C			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237119	ACGGGCACCCGCCAC[A/C]ACACCCGGCTAATTT	100507650
rs770447245	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23248045	GCTTACTCTTTGCTT[A/C]CAAGATAATGCCTTC	100507650
rs770492851	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23220741	GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGAT	100507650
rs770537720	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23190098	GAGCACCCACTCTCC[C/T]GGCTTCCCCCAACCT	100507650
rs770538523	in-del	-/CC	0.000134436	0.00819755	intron-variant	RNF212B	GRCh38.p7	14:23243320	AATGTAAGTTTTTCT[-/CC]CCCCCTGCCACAAAC	100507650
rs770607443	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23188837	TGCTCACTGCTGTAA[C/T]CCCAGTACCTAAAAT	100507650
rs770610112	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23189224	CTATTGTTTCATGGA[A/G]AAAATGGGAATAGGC	100507650
rs770694088	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23235265	TGAGGCAGAAGGATC[A/C]CTTGAGCCCAGGTAT	100507650
rs770780575	snp	A/G			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270237	TTCTCAAAAGTCCCT[A/G]TATTGAAAATGCTGG	100507650
rs770783465	in-del	-/T	0.000121087	0.00778004	intron-variant	RNF212B	GRCh38.p7	14:23262989	ACCTACACAGCAACA[-/T]TTAAAACTGTTGGCA	100507650
rs770803865	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23244665	TCTACGACTAAAGGT[G/T]GTTTTAGGGAGCTTT	100507650
rs770808897	in-del	-/TGCTCAATGTTGT			intron-variant	RNF212B	GRCh38.p7	14:23231940	GTCTCGTTCACTCAG[-/TGCTCAATGTTGT]TGCCCAGGCTGGAGT	100507650
rs770841198	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23243903	CCAACATGAGGAAAC[C/T]CTCGTCTCTACTAAA	100507650
rs770864770	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23229222	GCTGAATAATATTTT[-/A]TATATATATATATAT	100507650
rs770926070	snp	A/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184579	CTTGTTGTTCACAGC[A/T]CTTATTTAGGACTGG	100507650
rs770956254	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23257959	AAGCTTGAAAAACAG[-/T]TTTTAAAAAAAATCT	100507650
rs770963240	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23228351	ACAGGCTGGCCAGGC[C/G]CAGTGGATCACAGCT	100507650
rs770966048	in-del	-/AATAA			intron-variant	RNF212B	GRCh38.p7	14:23238768	AATAATAATAATAAT[-/AATAA]TAATAATAATCCCAC	100507650
rs770977297	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23263143	TATTAAAGATACTGT[A/C]CATTCAGGCAGGACA	100507650
rs771052616	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197299	TGGGAGGCTGAGGCA[A/G]GTGGATTTCATGAGG	100507650
rs771057321	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23271931	CGTAGTTATGTTTTT[A/T]AAAATAGCCTTTCTC	100507650
rs771058845	in-del	-/AAAAC			intron-variant	RNF212B	GRCh38.p7	14:23254288	ATACTCTTTATCTCA[-/AAAAC]AAAACAAAACAAAAC	100507650
rs771072776	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195324	AGGTAAATGTAAAGT[C/T]TCACAGATTTAGAAA	100507650
rs771081749	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23265790	TTTAGTCTATTTCCT[C/T]CCTTCTCATTATTTT	100507650
rs771121065	snp	A/G			splice-donor-variant, intron-variant	RNF212B	GRCh38.p7	14:23264235	GGTAGCTTGGGACAA[A/G]TAAGTAATGTTCACC	100507650
rs771126101	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23186202	CCTCTCTGTAGGTTG[C/G]AATCTTTTTGTGACA	100507650
rs771202964	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23216560	CAAACAAATAAATTA[A/T]GCTAAGTAAAAAAAA	100507650
rs771260148	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213784	GAGAGGCAGAGAGAG[-/A]AAAATGATTCAGCCT	100507650
rs771325121	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23231513	AAATGTAAAATCAAA[A/C]TTACAAATCTAGATT	100507650
rs771377017	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206796	ATACTCTGTCTTAAA[A/G]ACCCAAGAGTAGCCT	100507650
rs771382955	snp	A/G	0.000116164	0.00762028	intron-variant	RNF212B	GRCh38.p7	14:23270685	TGGCTAGTCTAACTT[A/G]TCTGTGCATAAAATC	100507650
rs771410285	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23222911	TACAAAAAATTAGCC[A/G]GGCATGGTGGCACGC	100507650
rs771430941	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23223814	TATCCTTGTTTGCAG[C/T]TGTCATAATTTTATA	100507650
rs771520671	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23224722	TGTAATACCCCACAA[C/G]CTCAGGCAACCAAAA	100507650
rs771528628	snp	A/G	0.000130847	0.00808743	intron-variant	RNF212B	GRCh38.p7	14:23244318	TGTATTGCTCTCTTC[A/G]TAGCTGAAGCCTCAG	100507650
rs771540753	snp	C/T	0.000116489	0.00763092	intron-variant	RNF212B	GRCh38.p7	14:23269000	TTTTCTTGGGATGTG[C/T]TCATACTTAAACTCT	100507650
rs771558270	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213903	CCCCAACAGTCAACA[A/G]GCACTAACATTTCAG	100507650
rs771687215	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211362	ATATAATTGAATTTG[C/T]AGCTAAAAATCTTCC	100507650
rs771688099	in-del	-/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215071	CAATGTGTTGAGGGA[-/G]GGACCTGGTGGGAGG	100507650
rs771699068	in-del	-/CT			intron-variant	RNF212B	GRCh38.p7	14:23250474	GGTGACAGAGCGAGA[-/CT]CTGTCTCAAAAAAAA	100507650
rs771755321	in-del	-/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23237131	ACCACACCCGGCTAA[-/T]TTTTTTTTTTTTTTT	100507650
rs771779595	snp	C/T			missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23259940	AATTTCTAGCCATTC[C/T]AAAGGTGAATGAAAT	100507650
rs771910819	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267319	TTTTCTCTTCAATTC[C/T]ATCAGTTTTTGCTTC	100507650
rs771933469	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23268533	TCTCATTGCTTTTAT[A/G]GAGGAGGAAATTTTT	100507650
rs771957304	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23189112	ACTGCCAGCAATCCT[A/T]CCACAATCTTGTAGT	100507650
rs772042630	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23220677	AAAAATACAGAAAAT[C/T]AGCTGGGCGTGGTGG	100507650
rs772109734	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23192754	TTTGGTGATAACTAT[A/G]CCTTTATGCCTTTAA	100507650
rs772112980	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23193755	AGAAGATTTAACAAA[A/C]AAAAAAAAGGAAGAA	100507650
rs772249326	snp	C/G	0.000259605	0.0113901	missense, utr-variant-3-prime, synonymous-codon, nc-transcript-variant	RNF212B	GRCh38.p7	14:23272857	GGCATATGGGATTAC[C/G]CAGTGGGAGAGAAGC	100507650
rs772309566	in-del	-/TAAG			intron-variant	RNF212B	GRCh38.p7	14:23231097	TTGTTTTGACTATTC[-/TAAG]TTTTTTGAAATTTTA	100507650
rs772322802	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244531	TTTCTTTGCTTTCTT[C/T]CTTGATGATACAAAT	100507650
rs772387717	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23264067	TGCTCTAGCCTGGGC[A/G]ACAGAGTGAGACTCT	100507650
rs772408088	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23226918	AGACTGCTAAGATTA[A/C]AGACATGAGCCATCA	100507650
rs772424568	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23227940	TTTTTTAAAAATCTC[A/T]TCAGGCAATGCCAGG	100507650
rs772426002	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205285	GGAATTAGACAAAAA[A/T]TTTTCTCTTTTTTTT	100507650
rs772456848	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23253284	GTTCCCACATTTTGA[A/G]TTGAGTTTCAATAAA	100507650
rs772488512	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23250311	TGGTAAAACCCTGTC[C/T]CTACTAAAAATACAA	100507650
rs772507123	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23191829	GCAGTTCTTGGCATA[C/T]AGAAGGCACTCGACA	100507650
rs772532683	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23254596	ATAGCATTTTGCCAC[A/G]TTGCCCAGGCTGTTC	100507650
rs772596218	in-del	-/AAAAC			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259198	ACTGTCTCAAAAACA[-/AAAAC]AAAAAAAAACATCTG	100507650
rs772640513	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204843	ATATTGATTCTACCC[A/C]TCCATGAGCATGGGG	100507650
rs772690416	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206561	CCTCACCCCCTTTTC[C/T]TTTTTCCTTTCTTAG	100507650
rs772695269	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23187736	CTCCATCCTTCTTCT[C/T]GTAACTATGTGCCCC	100507650
rs772750795	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211679	ATTGATTTAACATTC[-/A]AAAACAATGTAATTC	100507650
rs772832666	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23246932	GATCACCTGAGGTCC[A/G]GGGTTCGAGACCAGC	100507650
rs772845985	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23188631	ACCACTATGCCTGGC[-/A]AATTTTTAAAAAATT	100507650
rs772858094	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202017	GCACTTTGTGAGGCC[A/G]AGGTGGGTGGACTGC	100507650
rs772912525	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266799	GAATGTATATTCTAC[C/T]CTTTTTGGGTGGTGT	100507650
rs772935320	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23267468	CAGAGTCTCACTCTC[A/G]TCTTGGCTAGAGTGC	100507650
rs773003414	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208536	GAAAGTGCTCTTCCA[C/T]GGCCAAAGCTGGAAT	100507650
rs773016720	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184024	AGCCAATGTATTAAA[A/G]AATATTTAGGACTGG	100507650
rs773109236	in-del	-/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195278	AAGAAAAAAAAAAAA[-/T]CCCATGAGATGCAGC	100507650
rs773131415	in-del	-/CA			intron-variant	RNF212B	GRCh38.p7	14:23257154	CGAGACTCAGTCACA[-/CA]CACACAAAAAAAATA	100507650
rs773151910	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196482	GCCTGCTCTGTCACA[C/T]GGGCTGGAGGGCAGT	100507650
rs773175959	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23223989	GTAATCTTATTTACA[A/G]CAGCCACATATAAAA	100507650
rs773253418	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23255002	AGACCAAACCAAAAT[A/G]GAATTACTCATGCTG	100507650
rs773273390	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197976	ACATTCTTAAGGGCG[A/G]GGGAGATTACAAAGT	100507650
rs773333801	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23243859	ATGCGGGTGGATCAC[C/T]TGAGGTCAGGAGTTC	100507650
rs773403854	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184551	AAGATAAAAAACAAA[A/G]TCACCAGGTAGCCTT	100507650
rs773418595	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23225211	CACTGTTGGTGGGAA[C/T]GTAAATTAGTACAGC	100507650
rs773434855	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23227127	ATATAAGAAGTTATC[A/G]TTGGGGAAATAAATG	100507650
rs773452224	in-del	-/AATGTCTTCAA			intron-variant	RNF212B	GRCh38.p7	14:23193183	AAGTTTAAATGGAGC[-/AATGTCTTCAA]AATTGAGAAGGAATA	100507650
rs773467284	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23193994	TTACAGGAGCCTGCC[A/G]CTACGCCTGGCTAAT	100507650
rs773495882	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23231112	TAAGTTTTTTGAAAT[C/T]TTATATTAATTTTAG	100507650
rs773526883	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23216208	TCAAGATCGTGCCAC[C/T]GCACTCCAGCCTGGG	100507650
rs773543600	in-del	-/AAAA			intron-variant	RNF212B	GRCh38.p7	14:23251814	GTGAGACTCTGTCTC[-/AAAA]AAAAAAAAAAAGAAA	100507650
rs773575117	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23251828	TCAAAAAAAAAAAGA[A/C]AGAAAGAAAACCATA	100507650
rs773591832	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23229149	TTATTTCACTTAGCA[C/T]AATTTTTTCAAGATT	100507650
rs773686008	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23217349	AGCTGCACTAGGACA[A/T]CAGCTAAACTGCTAA	100507650
rs773704853	snp	A/G	0.000115148	0.00758687	splice-acceptor-variant, intron-variant	RNF212B	GRCh38.p7	14:23268923	TTTTTATGCTTTCCA[A/G]AAACCCCTTCACCGG	100507650
rs773717529	in-del	-/GA	0.00116891	0.0241472	intron-variant	RNF212B	GRCh38.p7	14:23244401	ACATCTCTCAGGTAT[-/GA]GAAACAAAAGTGAAG	100507650
rs773783502	snp	C/T	0.000722979	0.0189991	stop-gained, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23262678	AGGTCAATCACACCT[C/T]GACCAGTGGGCATTA	100507650
rs773854952	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23259016	GCGAGACTCTGTTTC[A/T]AAAAAAAAAAAAATT	100507650
rs773937688	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23272277	TACAAAAAATTAGCC[A/G]GGCATGGTGGCGGGC	100507650
rs773937790	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23257526	GAACAAAAAGTTTAT[A/G]AGAAGAGTACCAAGA	100507650
rs773941908	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23235335	AGCCTGGGCAGCAGA[A/G]GGAGACGCCCATCTC	100507650
rs773961742	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209156	AAGATAACTTCCTGA[C/T]GTTGCCATGGCATTT	100507650
rs773963751	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183618	TCTACTGCACAGCCG[A/G]CCCCATCCCTCTGGT	100507650
rs773996986	in-del	-/AAAA			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198519	GTCTCTACTAAAAAT[-/AAAA]AAAATCAGCTGGGCG	100507650
rs774034392	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23266596	ATTTTGTATTTTTAG[C/T]AGACACGGGGTTTCT	100507650
rs774038738	in-del	-/ATATGGTAAGCTT			upstream-variant-2KB, intron-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185609	TGCAAACTGATAACG[-/ATATGGTAAGCTT]ATATGGTAAGCTTTA	100507650
rs774078423	snp	A/C			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23199115	AGACAGGTCTCAGTT[A/C]ATTGTTTATTTTGCC	100507650
rs774129613	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23222527	AAGCCTGAGACCCAA[C/T]GGCTTCATTGCTGAA	100507650
rs774167992	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200385	GGCTAGAGTGCAATG[G/T]CATGATCTTGGCCCA	100507650
rs774169171	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23192554	GGTGGGGGGAGGGGG[A/G]AGGGATAGCATTAGG	100507650
rs774193481	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23253386	TAAGTTATTATTGAA[A/G]AAAATGGTCTTTTGT	100507650
rs774233083	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207092	TTTAAATCTTATTAC[C/T]ATATTTCAGCTAGGA	100507650
rs774280746	in-del	-/TAG	0.000773216	0.0196471	cds-indel, downstream-variant-500B	RNF212B	GRCh38.p7	14:23272885	AGCATGGACCACTTC[-/TAG]ATAGATCATCTTCAA	100507650
rs774377608	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196193	CACCATGGAAAAGTG[C/T]CTTTTACCAGGTGCC	100507650
rs774382738	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267185	CGAGGTCTCCCTGTT[C/T]TGCCCTGGCTGGTCT	100507650
rs774392298	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208066	GAATGGGAGGCAGGT[C/T]TGCCCTAAGCAGTTC	100507650
rs774466922	in-del	-/ATA/TCATC			intron-variant	RNF212B	GRCh38.p7	14:23238771	ATAATAATAATAATA[-/ATA/TCATC]ATAATAATAATCCCA	100507650
rs774468956	snp	C/G/T			intron-variant	RNF212B	GRCh38.p7	14:23268281	CAACCCTGTTCCATC[C/G/T]CCTCTAGTGACTGCC	100507650
rs774480046	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23209295	GTTTTACCAGCAAGG[C/T]CTTTATGACCTGTAT	100507650
rs774550197	snp	A/C			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215118	GCAGTTTCCCCCATA[A/C]TGTTCTCATGATGGT	100507650
rs774605660	in-del	-/C			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214491	AGAGTGAGACTCAGT[-/C]CCCCCAATAATTAAA	100507650
rs774611005	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213749	GAGAAGAAGTGAGGA[A/G]GAGAGGTAGAGAGAG	100507650
rs774638045	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202553	AAAGATGAGGCTTTA[A/T]TTGCTGTCAGTGTTT	100507650
rs774639379	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23261608	CCATGTTACAGGCTG[G/T]ATATATACCACCGGT	100507650
rs774641113	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23226728	GACCAGTCTCGTCTT[A/T]TCTCGGCTAGTCCCC	100507650
rs774652409	in-del	-/AAACAAAAC			intron-variant	RNF212B	GRCh38.p7	14:23254289	TACTCTTTATCTCAA[-/AAACAAAAC]AAAACAAAACAAAAC	100507650
rs774725197	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23262835	TAATATGAAAACATT[A/G]TATAACCAGATAACC	100507650
rs774731251	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23250698	GCCAAGATTGAGGAC[A/G]TGCGCCTCAGAAGGT	100507650
rs774793824	snp	G/T	0.000115694	0.00760484	intron-variant	RNF212B	GRCh38.p7	14:23268903	TGGATTATCTCACAG[G/T]CTTATTTTTATGCTT	100507650
rs774883611	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23255749	AGCAAACAAAAGTTA[A/G]TCTTCTTTGGAAAAA	100507650
rs774999127	in-del	-/AA			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202251	ACAAGACCCTGTCTT[-/AA]AAAAAAAAAAAAAAA	100507650
rs775057832	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23219540	GCAGTGGCAAGATCT[C/T]GGCTCACTGCAACCT	100507650
rs775070549	snp	G/T	0.000121249	0.00778523	missense, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240370	TTTCATTGCAACCAG[G/T]GCTTCCGAAAAGATG	100507650
rs775125820	snp	C/T	0.000124432	0.00788674	missense, utr-variant-5-prime, nc-transcript-variant	RNF212B	GRCh38.p7	14:23244341	AGCCTCAGGAGAAGA[C/T]GTTTTTCAAAAGTCC	100507650
rs775241251	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23186513	TGCCACCATGCCTGG[A/C]TAATTTTTGTGTTTT	100507650
rs775243838	snp	C/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210727	GGTTGCAGTGAGCCA[C/G]GATCACGCCATTGCC	100507650
rs775246722	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23257246	GGTCTCAAATTCCTG[A/G]CCTCAAGCAATCCTC	100507650
rs775335081	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197599	AAATTATTTAAAAAA[A/G]CAAATATAATTAAAA	100507650
rs775361276	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23229358	AATATTGGTGTACAC[A/G]TATCTGTTTGAGCCC	100507650
rs775378146	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23263917	ACATGGTGAAACCCT[A/G]TCTCTACTAAAAATA	100507650
rs775493521	snp	C/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23198999	GTGCTATACCTCACG[C/T]TGTCCACTGAGAGGG	100507650
rs775502903	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23187488	CGAGTAGCTGGGACT[A/G]CAGATGTGCGCCACC	100507650
rs775511316	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207986	TTTTGAGTTTCTGTT[A/C]GCCTTTCCAAAGGAG	100507650
rs775609106	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23218641	TCAGAGGAGACGAAA[G/T]AAAATAAAAAACAAT	100507650
rs775624000	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23239913	CGTGAGCCACTGTGC[C/T]TGGCCAGGATTGTAT	100507650
rs775630351	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213545	TGTCCCTCTGGGTAT[C/T]AGCAAATCACTGCAG	100507650
rs775630653	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23188894	TGATTGAATGAATTA[A/C]TGTATAAATAAATGT	100507650
rs775652919	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23266106	TGGGACTACAGGCAC[A/G]TGCCACCATGCTTGG	100507650
rs775698955	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207017	ACACACACATCTTGG[A/G]TGTGTTATCCTTTTA	100507650
rs775742829	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23253233	TCAAATTATCAGTCC[C/T]CATTCACATTTCTCC	100507650
rs775756013	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272469	GAAAATGTGAAAAAA[C/T]TTTAAAGTTATTGAA	100507650
rs775778077	snp	C/T			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273710	ACTAGGATCCCCATA[C/T]CCTTTCTGGTACTCT	100507650
rs775791221	snp	A/G	0.000121249	0.00778523	missense, synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23269937	ATTCAGGCCACACAA[A/G]AGTCCTCACCCCCAA	100507650
rs775847978	snp	A/G			intron-variant, nc-transcript-variant	RNF212B, LOC105370406	GRCh38.p7	14:23214033	GAGGCTAGCACAGGA[A/G]GATCACTTGAGCCCA	100507650
rs775848181	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23250470	CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCAAA	100507650
rs775900039	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23261498	ACTCATCCTTCAAAA[C/T]TGAACTCAGTCATTT	100507650
rs775919879	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23241161	CAGTAGGGTTTTGAA[C/T]GATAAAATGGAATTT	100507650
rs775938095	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23224892	ACTATATAAGGAGCT[C/G]AAACAACTCTATGGG	100507650
rs775991732	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23248938	AGGCCATACAATTTC[C/T]GATGCTGCTACCCAA	100507650
rs776030873	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23267705	AAGTGCTGAGGATTA[C/T]AGGCATGAGCCACTG	100507650
rs776099280	snp	A/C/G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202143	GTAATCCCAGCTATT[A/C/G/T]GGGAGTCTGAGGCAG	100507650
rs776102338	snp	C/T	0.000120941	0.00777534	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260733	GCCCCCTGAAAATTC[C/T]TGTTCTTTCTTGACT	100507650
rs776134426	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23216877	TGAATGTGACCCTGT[-/C]TCAAAAAAAAAAAAA	100507650
rs776274992	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23234294	ACTTTGTGCTTTACT[C/T]TTCGTGTGTGTGTGT	100507650
rs776287042	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23235365	CTTAAAAACAATTAT[A/G]TTTAAGAAAACTATT	100507650
rs776297742	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23190189	TATCCTCCCTCTCTA[C/G]CTGTGTGATGTCATC	100507650
rs776387342	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23268688	GGCACAGATACATGA[A/G]AGCACATGAAGGCAG	100507650
rs776399539	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23255332	TTTGTTGTAATTTTG[C/T]ATTTTGACATGTTAT	100507650
rs776416597	in-del	-/AA			intron-variant	RNF212B	GRCh38.p7	14:23218370	AGAGTCTATCTCAAA[-/AA]AAAAAAAATAAATAA	100507650
rs776435796	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23188856	AGTACCTAAAATGGT[G/T]CCTGGCACTCAATAA	100507650
rs776502738	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244758	CTGCAAACAATAGGT[C/T]TGATGGTTTAACTTG	100507650
rs776526900	in-del	-/AA			intron-variant	RNF212B	GRCh38.p7	14:23233743	TGAGACCCTGTCTCA[-/AA]AAAAAAAAAAAAAAA	100507650
rs776551379	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196720	GTGCTGGGATTACAG[A/G]CATGAGCCACTGTTC	100507650
rs776560567	snp	C/T			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184695	GGGGAATTATCAGTA[C/T]ATCGCTGATCATGAA	100507650
rs776577882	in-del	-/TGGCAGTGGT			intron-variant	RNF212B	GRCh38.p7	14:23217246	CAGTGGTGGCAGTGG[-/TGGCAGTGGT]GGGGGGGGGGCTCCT	100507650
rs776652211	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23191348	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	100507650
rs776673043	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23228462	AACCCTATCTCTACC[-/A]AAAAAAAAAAAAAAA	100507650
rs776679874	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23218469	AAGCAGAAGAAAGAA[C/T]TAGTGAGTTTGAAGA	100507650
rs776740037	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23228353	AGGCTGGCCAGGCGC[A/G]GTGGATCACAGCTGT	100507650
rs776760968	in-del	-/TT			intron-variant	RNF212B	GRCh38.p7	14:23248440	CCAACCCCAAGCCTC[-/TT]TTTTTTTTTTTTTTT	100507650
rs776767891	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23226193	ATCCCAGTTACTCGG[A/G]AGGCTGAGGCAGGAG	100507650
rs776769563	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23251963	TCACCAACTTGGTAA[C/T]TCTCTGAACCGCCTT	100507650
rs776780536	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23224354	TGACTTCAAATTATA[C/T]TGCAGAGCTAAAGTA	100507650
rs776853987	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23238893	TGTCTAACACAAAAG[A/T]TATTTAATGTGGGAG	100507650
rs776955171	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23272188	TTTGGGAGGCCGAGG[C/T]GGGCGGATTATGAGG	100507650
rs776975612	in-del	-/AG			intron-variant	RNF212B	GRCh38.p7	14:23233348	CCTTCCCTCCACTAT[-/AG]TGTCCTATGACCCTG	100507650
rs777026693	snp	C/T	0.000142359	0.00843559	intron-variant, utr-variant-5-prime	RNF212B	GRCh38.p7	14:23258546	CTTGTTTTTCCCTAG[C/T]AGGTGTGGAGTTTCC	100507650
rs777159058	in-del	-/CTA			downstream-variant-500B, cds-indel	RNF212B, HOMEZ	GRCh38.p7	14:23274426	CTTTGTAACACAATT[-/CTA]CTGTTTAAAAGGACA	100507650
rs777169624	snp	A/G			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215375	GTTTCCTATGGAGAA[A/G]CAAAGATTCAAATGA	100507650
rs777173125	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23194338	TTGAACTTCTAAGTA[C/T]CTAAAAATAAGGCTT	100507650
rs777193447	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214331	AAACCCCGTCTCTAC[C/T]AAAAATACAAAAGTT	100507650
rs777212648	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23183378	TTTTCTTTTATGATG[A/G]AGACAAAAGTAGTTT	100507650
rs777241596	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23224831	AATCCACAGAATGAG[A/G]GAATATATTTGCAAA	100507650
rs777261590	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23231726	TGCCATCTCGGCTCA[C/G]TGCAACCTCCCTGCC	100507650
rs777306798	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23242779	AGGAGTTCAAGACCA[C/G]CTTGAGCAACATAGG	100507650
rs777323749	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23225847	AAGTATAATTGGATT[A/G]TTTGTAACACAAAGG	100507650
rs777389265	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23225953	ATATCTCATGTACCC[C/T]GTAAGTATACACACC	100507650
rs777422522	in-del	-/AT	0.000311413	0.0124744	intron-variant	RNF212B	GRCh38.p7	14:23262882	CCAGGCAAGGCAGGC[-/AT]ACCATTGATGGCAAC	100507650
rs777468657	snp	G/T	0.000552537	0.0166121	intron-variant	RNF212B	GRCh38.p7	14:23258705	GAGCTTTTTTTTTTT[G/T]TTTTTTTCTAAGAAG	100507650
rs777493210	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23190024	GTCCAATCTAGCAAT[A/C]ATTTCTCAGTCTTTA	100507650
rs777564811	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23200017	ACATAATAAAAAATT[-/A]AAAAAAAAAAAAATT	100507650
rs777667321	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23204657	GAAATCAGTTAGTGT[G/T]ATACCTCCAGATTTG	100507650
rs777670403	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198633	GTGAGCCGAGATCGC[A/G]CCATGGCACTCCAGC	100507650
rs777680347	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23249888	CTGAACCGTCACGAT[A/C]ATCTATTTCAATTAC	100507650
rs777698001	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23221509	CAAATATTATTAGAG[C/G]TAAAGAGAAAGACAG	100507650
rs777726357	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23244571	TTAACTTTTTATTGA[C/T]CCAGAATCTGTGATA	100507650
rs777741142	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23190983	CCGTCTTGGGGGTGT[C/T]CTCCCTTTCTCACAT	100507650
rs777741828	snp	A/C			intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270167	TAGCACTCATCCTGT[A/C]ACCAGTCGAGTCCTA	100507650
rs777768240	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236481	GATGGCGCCACTGCA[C/T]TCCAGCCCTGGCGAC	100507650
rs777813317	snp	C/T			utr-variant-5-prime, intron-variant	RNF212B	GRCh38.p7	14:23237985	CTTTCCCGCCATGTC[C/T]AGCTCTTCGTGAGGA	100507650
rs777826269	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236854	CAATATAAGGGGATA[C/T]AAATTTCTGGGATCA	100507650
rs778008939	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23265720	TCATTTCAAAGAATT[C/T]GTTTTGTTGAGAGTC	100507650
rs778064504	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23230026	TGATTTTATTATCAG[C/T]TTTCATCCAAATCCA	100507650
rs778080602	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206651	TTAAATTTGCACATT[A/G]AAGGAAACAACTCAG	100507650
rs778100666	in-del	-/AAT			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23214669	TGAACTTGAAGATAA[-/AAT]AATAATAATAATAAT	100507650
rs778130314	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23257041	GCCTGTAATCCCAGC[A/T]ACTCAGGAGGCTGAG	100507650
rs778134000	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23207055	TGATTTTTAACCATT[A/G]AGCTGCTTAAAATTT	100507650
rs778145169	snp	C/T			synonymous-codon, intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23240360	AATGGATTGGTTTCA[C/T]TGCAACCAGTGCTTC	100507650
rs778150413	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23194262	AGGCAAAAAGCATCA[A/G]TATATATAAAGGAGG	100507650
rs778156261	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23222228	AAAAGATGAACAAAA[C/T]TGATAAACTTTTAGC	100507650
rs778166250	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23187130	CGGAGCCACTGTTTC[A/G]GCTGTTTTGCGTGCT	100507650
rs778167905	snp	C/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	SLC7A8, RNF212B	GRCh38.p7	14:23185345	GAAATGAAAAAATGT[C/G]GAATTTGCCTCTAGC	100507650
rs778177374	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23229037	TCTCTCATACCCCTA[C/G]TTCCTGCTAACCTCT	100507650
rs778189502	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23264165	TTCTTTTTGTTTCAC[C/T]TTATACAGTCGGTCC	100507650
rs778332157	snp	A/T	0.000138802	0.00832957	intron-variant	RNF212B	GRCh38.p7	14:23244301	TGGATATTCTCACAG[A/T]GTGTATTGCTCTCTT	100507650
rs778360316	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23239512	CTTTCTGGTTCACTA[A/C]CTTCTCTTGGCTCCA	100507650
rs778364553	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23253680	TGTAAAATTCCAATT[A/C]TGTCATCCTTTCTTA	100507650
rs778403874	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195820	TTTCGTTTAACCTTC[C/T]AAACAACCTTTCAAG	100507650
rs778512125	snp	C/G	9.79768e-05	0.00699848	splice-acceptor-variant, intron-variant	RNF212B	GRCh38.p7	14:23264173	GTTTCACCTTATACA[C/G]TCGGTCCTCCTCAGC	100507650
rs778539192	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23223711	TTTTCACCACTGTTA[C/T]TCAACATAGGACTGG	100507650
rs778547432	snp	C/T			intron-variant, downstream-variant-500B	RNF212B, LOC105370406	GRCh38.p7	14:23195165	AGGTGTTGTGGTGCA[C/T]GTCTACAGTCCCAGC	100507650
rs778572520	in-del	-/CTG			intron-variant	RNF212B	GRCh38.p7	14:23255936	CATCAGGCAAAATCA[-/CTG]CTTCTTTAATACTCC	100507650
rs778599166	snp	C/G			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273183	AAAAAATAATTCTTG[C/G]CATCATGCTTGGTTG	100507650
rs778600411	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23225856	TGGATTGTTTGTAAC[A/G]CAAAGGATAAAAGCA	100507650
rs778622429	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196304	CAGCCTGCCCCGCTC[C/T]GCCATTATCATGCCA	100507650
rs778677814	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23249575	TTTTGAAGAAAAGTT[A/G]TATTTAGTTTGATAT	100507650
rs778780725	snp	A/G			utr-variant-3-prime, downstream-variant-500B	RNF212B, HOMEZ	GRCh38.p7	14:23273518	ATGGTGGAATGGGCG[A/G]ACAACACTATCACTG	100507650
rs778786308	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23248682	CCTGACCTCGTGATC[C/T]GCCCACCTCAGCCTC	100507650
rs778833095	snp	C/T			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236342	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	100507650
rs778843146	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23268406	CCACAAACCTTGCTG[C/T]TTTTACTAACATTTT	100507650
rs778848615	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23260951	GAACATAAATTTAAT[C/T]TACTCAGCAAGGTCA	100507650
rs778859704	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23254751	ACATTGGACCAAAAC[A/G]TCTTGTCTTATCATA	100507650
rs778868137	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23235010	CGAGGTCAAGAGTTT[C/G]AGACCAGCCTGGCCA	100507650
rs778889099	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201895	GTAAGCAATCTATAA[A/C]GTTTATTCTTGAGTA	100507650
rs778937601	snp	A/G	0.000123251	0.00784924	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23259923	GAATGGAGAACTGAA[A/G]AAATTTCTAGCCATT	100507650
rs778974939	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23189057	TTTTGACTTTGAAGA[C/T]TATTTTATACAGAGC	100507650
rs778979212	in-del	-/CTT			intron-variant	RNF212B	GRCh38.p7	14:23247226	TTTTCATGCAATCAC[-/CTT]CTTTTTTAATAACAG	100507650
rs779027548	snp	G/T			missense, nc-transcript-variant	RNF212B	GRCh38.p7	14:23258628	AGTTAGAAACAGCCA[G/T]GCAGGAGGCACAGCA	100507650
rs779045333	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23210431	AAAGTCTGGAGTTTA[A/G]TTAATTATAATGTGC	100507650
rs779056584	snp	C/T	0.000122812	0.00783525	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270000	GAATGGAGCTTCAAC[C/T]ATAGACACATATACT	100507650
rs779088265	in-del	-/CGT			intron-variant	RNF212B	GRCh38.p7	14:23256938	GCAGGTGGATCACGA[-/CGT]GGTCAGGAGTTCGAG	100507650
rs779109345	in-del	-/AA	0.000121058	0.0077791	frameshift-variant, intron-variant, upstream-variant-2KB, nc-transcript-variant	RNF212B	GRCh38.p7	14:23260674	AATCTCCAAGTCGGT[-/AA]ACCAAGGAAGCAGGT	100507650
rs779133368	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211462	GCCAATTCTACACAA[A/C]TACTCCCCAAAAGTT	100507650
rs779151248	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23256635	CCTTGGTCTCCCAAA[C/G]TGCTAGGATTACAAG	100507650
rs779171432	snp	A/G			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184946	AAATTATTTAATTTT[A/G]AAGTGGGCCTAAAAA	100507650
rs779232598	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23243420	AGAAAAGAAGACCGG[A/G]CGTGGTGGCTCAGGC	100507650
rs779260920	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23185707	GGTACTAGGTGCACA[C/T]GTTGGAAAGGAAGAG	100507650
rs779309815	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205106	TTTTTATTTTAGGAC[G/T]AAACATTTACTATAA	100507650
rs779386004	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23244454	ATTCTAATTGCATCT[G/T]ATTCCTTTATCAAAG	100507650
rs779394827	snp	A/C			upstream-variant-2KB	SLC7A8, RNF212B	GRCh38.p7	14:23184343	AAATTTTAAAATTAG[A/C]CGGGTGCAGTGGTGC	100507650
rs779495370	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23254290	CTCTTTATCTCAAAA[-/A]ACAAAACAAAACAAA	100507650
rs779529073	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23239348	TACAGGTGTGAGACA[C/T]CATGCTTGGCCTGAT	100507650
rs779531733	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23265224	TGGTCAGGAGATGGA[A/G]GATAACTTTTCAGTA	100507650
rs779537621	snp	A/T	0.000163599	0.00904283	intron-variant, upstream-variant-2KB	RNF212B	GRCh38.p7	14:23259994	TCTCTTACTTTTCTC[A/T]TCTATCTAGCTGACT	100507650
rs779575705	in-del	GCCAATCTTATTCTGTCTCTCTC/TT			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236939	GTGGAGAAATCTGAT[GCCAATCTTATTCTGTCTCTCTC/TT]TTTTTTTTTTTTTTT	100507650
rs779612796	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23271895	TTGTTAACATTGGAG[A/T]GTTTTTTGGTATGAT	100507650
rs779634566	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23238593	AAAAATAAAAAATAG[C/G]CAGGCGTGGTGGTGC	100507650
rs779653671	snp	G/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206370	GAGCCACCGTGCCCG[G/T]CCTAGTCTTTTCTTT	100507650
rs779658853	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23247636	AATAATAATCTATTA[C/T]ATAAATGGATATACA	100507650
rs779828025	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23233278	ACACTGCGGAAGGCC[G/T]CAGGGTCCTCTGCCT	100507650
rs779905561	in-del	-/AG			intron-variant	RNF212B	GRCh38.p7	14:23256510	CCATTAGCTGGAATT[-/AG]ACAGGTGCACGCCAC	100507650
rs779962569	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23224284	ACAACAGAAGACCCA[C/G]AATAGCCAAAGCTAT	100507650
rs780040196	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23262247	GGATCTAGGAAATAT[-/A]GACCCAAATATATGC	100507650
rs780059949	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23213474	TCCAATAAAAATTCC[A/G]CCAGGAGTCATGAGG	100507650
rs780169407	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23234961	GCTCATACCTGTAAT[C/T]CCAGCACTTTGGGAG	100507650
rs780231693	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206631	CAGTTGTCAGCTAAA[C/T]AGCCTTAAATTTGCA	100507650
rs780298164	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23243173	CCTTTGCTAGCATAC[A/T]AGATTGTTGCCATGT	100507650
rs780455058	snp	G/T	0.000915751	0.0213784	intron-variant	RNF212B	GRCh38.p7	14:23243313	TTTCTGATAATGTAA[G/T]TTTTTCTCCCCCTGC	100507650
rs780469066	snp	A/C			intron-variant	RNF212B	GRCh38.p7	14:23268212	GTCTTCCAGGGAACC[A/C]CTAGACAGGTCAAAT	100507650
rs780526442	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23219503	TTTTGAGACAGTCTC[A/T]CTCTGTCGCGCAGAC	100507650
rs780528571	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23240229	ATACCCACAATGATA[C/T]GCCACATCCCAAAAA	100507650
rs780533856	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196085	TTGGTCACATCCTCA[A/G]TTGCTGCTGTCTACT	100507650
rs780555610	snp	A/G	0.000115627	0.00760264	intron-variant, nc-transcript-variant	RNF212B	GRCh38.p7	14:23270586	ATCTTTCACTGTTCC[A/G]TTCTATCCTTCAGCT	100507650
rs780687973	in-del	-/ATC/ATCATCATA/ATCATCATC			intron-variant	RNF212B	GRCh38.p7	14:23238783	ATAATAATAATAATC[-/ATC/ATCATCATA/ATCATCATC]CCACAAAGAAACCTT	100507650
rs780705069	in-del	-/TCTTTTTTT			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236960	CTTATTCTGTCTCTC[-/TCTTTTTTT]TTTTTTTTTGTTTGA	100507650
rs780853115	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206240	CCACCATGGCCAGCT[A/C]ATTTTTGTATTTTTA	100507650
rs780903422	snp	A/C	9.36198e-05	0.00684114	intron-variant	RNF212B	GRCh38.p7	14:23268898	GTTCATGGATTATCT[A/C]ACAGGCTTATTTTTA	100507650
rs780943472	snp	C/G			upstream-variant-2KB, intron-variant	RNF212B	GRCh38.p7	14:23236553	AAAAGCAAAAAAACC[C/G]CAAACAACAACAACA	100507650
rs781022837	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23193904	TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG	100507650
rs781104831	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23238079	TGTAGCCAGAAAAAG[A/T]ACTGAGAAGCTTGAG	100507650
rs781116524	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203054	TTCTTTAGTGGTGAT[C/T]TGTGAGATTTTGGTG	100507650
rs781120485	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23212094	AATATCCAATCCTGA[C/T]TTTAAAAAAATCTCA	100507650
rs781155694	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23258000	ACGGGATGAAAAATT[A/G]TATATTTAAAGGGTC	100507650
rs781156382	snp	A/G			downstream-variant-500B, utr-variant-3-prime	RNF212B, HOMEZ	GRCh38.p7	14:23274563	AACAATGAACAGAGT[A/G]AGGATTTTGGAAAGA	100507650
rs781171380	snp	A/C			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23199921	CATGGGAAAAAAAGA[A/C]GGGAAAAAAAAGAAA	100507650
rs781247579	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23252422	TGTAATTTCAAATGT[C/T]TAAAAGAATATAATG	100507650
rs781264353	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23247514	ATCATATAATGTATG[G/T]TCTTTTGTGACTTGC	100507650
rs781329157	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23238657	GTGGGAAGATCGCTT[A/G]AGCCCAGGAGTTCCA	100507650
rs781425113	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23253798	TGCTTGTAGATATTA[C/T]GGAATGAGGGAGTTT	100507650
rs781427673	in-del	-/TTTA			intron-variant	RNF212B	GRCh38.p7	14:23191981	AGGATTTTACAGAGT[-/TTTA]CTGCCCTTTCAGGCC	100507650
rs781436466	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23231004	TATGCTAGAAACACA[C/T]TGTTTTGATTACAGT	100507650
rs781511195	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23240747	GGGAAAAGAGATAGA[A/G]TAAGTATAATGGATG	100507650
rs781614118	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23265793	AGTCTATTTCCTTCC[G/T]TCTCATTATTTTGGA	100507650
rs781616549	snp	C/T			intron-variant	RNF212B	GRCh38.p7	14:23252983	GTAATTCTTGTTAAA[C/T]CCTATGAGGACGGTT	100507650
rs781674147	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23225648	AGGATGGTTATTAGA[A/G]GCGGGGAAGGGTAGT	100507650
rs781688506	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23267027	ATGCTGGAGTGTAGT[C/G]GCACAATTGTGGCTC	100507650
rs781714227	snp	C/T			intron-variant, upstream-variant-2KB	RNF212B, LOC105370406	GRCh38.p7	14:23215852	TCTCCTAGTCCTTAT[C/T]CATTCTTAGTGAGTT	100507650
rs781758883	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23258883	CCTCTTCTATTTCTC[A/G]GTATCAAAAACTGCT	100507650
rs781765272	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195963	CACTGCATTTGCTCT[A/T]TTCACTGTGCCACGG	100507650
rs796100643	in-del	AAAAAAAT/CACACAA			intron-variant	RNF212B	GRCh38.p7	14:23257156	GACTCAGTCACACAC[AAAAAAAT/CACACAA]AAAAATAAAATAAAA	100507650
rs796167563	snp	C/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23197865	GTCAGCGAAGGGAGA[C/T]AGGGGTGGGGCCATT	100507650
rs796182147	snp	G/T			intron-variant	RNF212B	GRCh38.p7	14:23224260	AAGCTATCCTAAAAT[G/T]TGTATGAAACAACAG	100507650
rs796195872	in-del	-/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23211228	TCTCAAAAAAAAAAA[-/G]GAAAGAAAAAGCAAC	100507650
rs796256336	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242097	AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAGAAAA	100507650
rs796266598	in-del	-/TGTTAAG			intron-variant	RNF212B	GRCh38.p7	14:23255525	GCATTATCCAGACAA[-/TGTTAAG]TGTTATCATCAATAG	100507650
rs796287848	snp	A/G			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23196367	AGCCCACTCTGCGTC[A/G]CCACTGCTCTCTGTG	100507650
rs796307787	snp	C/G			intron-variant	RNF212B	GRCh38.p7	14:23188581	AAGTGATCCTCCTGC[C/G]TCAGCCTCTCAAGTA	100507650
rs796329912	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23202850	GCGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	100507650
rs796346488	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23266639	TGGTCTCAAACTCCT[A/G]ACCTCAGGTGATCTG	100507650
rs796377951	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23203361	GATTTTGCAATTGTG[-/A]ATTGTGCTGCTATAA	100507650
rs796401098	snp	A/T			intron-variant	RNF212B	GRCh38.p7	14:23229240	TATATATATATATAT[A/T]TATATATATATATAT	100507650
rs796402453	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23186360	CATTTTTTTTTTTTT[-/T]GAGAAGGAGTCTCGC	100507650
rs796425344	in-del	-/CA			intron-variant	RNF212B	GRCh38.p7	14:23254292	TCTTTATCTCAAAAA[-/CA]AAACAAAACAAAACA	100507650
rs796444520	multinucleotide-polymorphism	AG/GA			intron-variant	RNF212B	GRCh38.p7	14:23242107	AAAAAAAAAAAAAAA[AG/GA]AAAGAAAAAGAAAAA	100507650
rs796446892	in-del	-/AT			intron-variant	RNF212B	GRCh38.p7	14:23257164	CACACACACACAAAA[-/AT]AAAATAAAATAAAAT	100507650
rs796461808	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23195266	ACTCTGTCTCTAAAG[-/A]AAAAAAAAAAAACCC	100507650
rs796484963	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23242813	ACTCCATCTCTAAAG[A/G]TAATAACAAAATTAA	100507650
rs796490862	in-del	CAACAATT/GAA			intron-variant	RNF212B	GRCh38.p7	14:23251246	ACCAACTAGGTATGC[CAACAATT/GAA]AATTCAATTCAATTC	100507650
rs796525803	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23251815	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAGAAAG	100507650
rs796546106	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23222018	AATGTATAGCTATAA[A/G]TGTCTACATCAAAAA	100507650
rs796548916	in-del	-/AC			intron-variant	RNF212B	GRCh38.p7	14:23254291	CTCTTTATCTCAAAA[-/AC]AAAACAAAACAAAAC	100507650
rs796551752	multinucleotide-polymorphism	GA/TG			intron-variant	RNF212B	GRCh38.p7	14:23230044	CATCCAAATCCACTG[GA/TG]GAATGGGATGATTTT	100507650
rs796608176	in-del	-/AAAAAC			intron-variant	RNF212B	GRCh38.p7	14:23220234	AACAAAAACAAAAAC[-/AAAAAC]CATACAACAAGGCCA	100507650
rs796619830	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23226718	CGTGGTGCTGGACCA[A/G]TCTCGTCTTATCTCG	100507650
rs796635661	in-del	-/C			intron-variant	RNF212B	GRCh38.p7	14:23257156	AGACTCAGTCACACA[-/C]ACACAAAAAAAATAA	100507650
rs796649016	multinucleotide-polymorphism	AGG/GGC			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208828	AATGGCGCGATCTCA[AGG/GGC]CACTGCAAGCTCTGC	100507650
rs796651121	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23188461	TGACAAAGATTAGGG[-/T]TTTTTTTTTTTTTTT	100507650
rs796661846	in-del	-/ATCATCATC			intron-variant	RNF212B	GRCh38.p7	14:23238768	ATAATAATAATAATA[-/ATCATCATC]ATAATAATAATAATC	100507650
rs796688509	in-del	-/A			intron-variant	RNF212B	GRCh38.p7	14:23193751	AGTAGAAGATTTAAC[-/A]AAAAAAAAAAAAGGA	100507650
rs796743075	snp	A/G			intron-variant	RNF212B	GRCh38.p7	14:23240568	AATGGTGATAAAGAT[A/G]CTGTAGGAAACTGTC	100507650
rs796743695	in-del	-/CCTC			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23205603	CCATATTGCTCTTAA[-/CCTC]CAAGCTGTCCTTGTT	100507650
rs796800831	multinucleotide-polymorphism	CA/TG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206221	TGGGATTATAGGTGC[CA/TG]ACCACCATGGCCAGC	100507650
rs796871318	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23206913	AAACAAACTTTCGTT[-/A]AAAAAAAAAAGACAA	100507650
rs796900884	multinucleotide-polymorphism	AA/CC			intron-variant	RNF212B	GRCh38.p7	14:23263754	GTGCCCCTTCCCCCA[AA/CC]AAAAACGAGTGTTCT	100507650
rs796972364	multinucleotide-polymorphism	CCA/TCG			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23208958	GAGACGGGGTTTCAT[CCA/TCG]GTTAGCCGGGATGGT	100507650
rs796988789	in-del	-/T			intron-variant	RNF212B	GRCh38.p7	14:23264778	TCACTTGTTTTTTTT[-/T]CCTGACAGTGATTCC	100507650
rs796990344	in-del	-/A			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23198684	TCCAAAAAAAAAAAA[-/A]GGTCCACGTACTGTA	100507650
rs797020197	snp	A/T			intron-variant	RNF212B, LOC105370406	GRCh38.p7	14:23201458	GTTATATTAGAATTA[A/T]AAGTTTCTCATAATT	100507650

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