Variant report

Variant	rs10420011
Chromosome Location	chr19:20140614-20140615
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 128 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs1008112	0.86[CEU][hapmap]
rs1019280	0.86[CEU][hapmap]
rs10404484	0.82[EUR][1000 genomes]
rs10408129	0.88[EUR][1000 genomes]
rs10409512	0.87[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10409629	1.00[ASW][hapmap];0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];0.86[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10410313	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10416812	0.93[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap]
rs10418140	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10419467	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10420124	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10420900	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10423526	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10423976	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11085293	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11085294	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1121387	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1121388	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11666112	0.86[CEU][hapmap]
rs11668688	0.81[ASN][1000 genomes]
rs11671950	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12151060	0.86[CEU][hapmap]
rs12463237	0.86[EUR][1000 genomes]
rs12610295	0.86[CEU][hapmap]
rs12977293	0.82[JPT][hapmap]
rs12977326	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12983056	0.93[ASW][hapmap];0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.82[GIH][hapmap];0.87[JPT][hapmap];0.89[TSI][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1319479	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17767339	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1860939	0.93[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1860940	0.93[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.80[EUR][1000 genomes]
rs1974650	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1974651	0.88[EUR][1000 genomes]
rs1987408	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2017721	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2041606	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2110124	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2110125	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2110587	0.86[CEU][hapmap]
rs2110589	0.86[CEU][hapmap]
rs2215721	0.84[EUR][1000 genomes]
rs2286920	0.86[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2286921	0.86[CEU][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2286922	0.85[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2286923	1.00[ASW][hapmap];0.86[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.91[JPT][hapmap];0.84[MEX][hapmap];0.87[TSI][hapmap];0.82[YRI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2335888	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2335889	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2335890	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2335892	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2335896	1.00[ASW][hapmap];0.93[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.91[JPT][hapmap];0.84[MEX][hapmap];0.90[TSI][hapmap];0.82[YRI][hapmap];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2335897	1.00[ASW][hapmap];0.93[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];0.84[MEX][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs258575	0.87[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs258579	0.87[CEU][hapmap]
rs2878552	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4563152	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4809005	0.86[CEU][hapmap]
rs4809014	0.86[CEU][hapmap]
rs4809023	0.87[AFR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5013556	0.88[EUR][1000 genomes]
rs6511066	1.00[CEU][hapmap];0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6511067	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6511069	1.00[ASW][hapmap];0.93[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.87[JPT][hapmap];0.84[MEX][hapmap];0.89[TSI][hapmap];0.82[YRI][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6511070	0.90[EUR][1000 genomes]
rs6511071	0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.80[GIH][hapmap];0.80[TSI][hapmap];0.88[EUR][1000 genomes]
rs6511072	0.92[CEU][hapmap];0.95[CHB][hapmap];0.88[EUR][1000 genomes]
rs6511073	0.93[CEU][hapmap];0.95[CHB][hapmap];0.86[EUR][1000 genomes]
rs6511074	0.93[CEU][hapmap];0.95[CHB][hapmap];0.86[EUR][1000 genomes]
rs6511075	0.86[EUR][1000 genomes]
rs6511076	0.93[CEU][hapmap];0.95[CHB][hapmap];0.83[EUR][1000 genomes]
rs71944124	0.88[ASN][1000 genomes]
rs7246955	0.93[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.82[EUR][1000 genomes]
rs7247476	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7247483	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7247572	0.93[ASW][hapmap];0.93[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7247818	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7247843	0.92[ASN][1000 genomes]
rs7248117	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7248186	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7250923	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7251276	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7256046	0.93[CEU][hapmap];0.95[CHB][hapmap];0.90[EUR][1000 genomes]
rs8101213	0.93[CEU][hapmap];0.95[CHB][hapmap];0.88[EUR][1000 genomes]
rs8101367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8103577	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs8103855	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8104703	1.00[ASW][hapmap];0.93[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.91[JPT][hapmap];0.84[MEX][hapmap];0.90[TSI][hapmap];0.82[YRI][hapmap];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8104933	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8106159	0.89[EUR][1000 genomes]
rs8106259	0.89[EUR][1000 genomes]
rs8106847	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8107041	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8109457	0.82[CEU][hapmap]
rs8109906	0.94[ASN][1000 genomes]
rs8112738	0.93[CEU][hapmap];0.95[CHB][hapmap];0.90[EUR][1000 genomes]
rs8182568	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9304964	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9304965	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs963380	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs993044	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519535	chr19:19871250-20595412	Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
2	esv3319016	chr19:19917475-20819154	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
3	esv3319017	chr19:19917475-20819154	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
4	nsv1061846	chr19:19946927-20595412	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
5	esv3390957	chr19:19965887-20819154	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
6	nsv869122	chr19:19969851-20595412	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1057569	chr19:19973268-20193556	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	nsv1059158	chr19:19973489-20576161	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
9	nsv458376	chr19:20021046-20151257	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv578800	chr19:20021046-20151257	Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv911319	chr19:20025940-20170214	ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv870354	chr19:20043821-20576175	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
13	nsv1062018	chr19:20053658-20193556	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
14	nsv1066004	chr19:20053658-20592867	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
15	nsv543932	chr19:20053658-20592867	Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
16	nsv1066564	chr19:20056348-20595412	Weak transcription Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
17	nsv1066375	chr19:20061084-20574512	Strong transcription ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
18	nsv543934	chr19:20061084-20574512	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
19	esv3501977	chr19:20072180-20193556	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
20	esv3501978	chr19:20072180-20193556	Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
21	nsv1057309	chr19:20072886-20595412	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
22	nsv578801	chr19:20084681-20595412	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
23	nsv1055694	chr19:20088866-20595412	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
24	nsv578802	chr19:20091702-20595412	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
25	nsv1066970	chr19:20093894-20164335	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
26	nsv1062725	chr19:20097317-20157102	Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
27	nsv1064400	chr19:20101052-20595412	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
28	nsv911322	chr19:20111134-20193556	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
29	nsv578803	chr19:20116963-20160115	Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs10420011	SAGE1	trans	parietal	SCAN
rs10420011	ZNF506	cis	cerebellum	SCAN
rs10420011	ZNF682	cis	cerebellum	SCAN
rs10420011	ATP13A1	cis	parietal	SCAN
rs10420011	F2RL3	cis	parietal	SCAN
rs10420011	SLC27A1	cis	cerebellum	SCAN
rs10420011	ZNF253	cis	Nerve Tibial	GTEx
rs10420011	ZNF682	cis	Lymphoblastoid	GTEx
rs10420011	ZNF682	cis	multi-tissue	Pritchard
rs10420011	ZNF682	cis	parietal	SCAN
rs10420011	ZNF682	cis	lymphoblastoid	seeQTL
rs10420011	ZNF682	cis	Muscle Skeletal	GTEx
rs10420011	ZNF100	cis	cerebellum	SCAN
rs10420011	ZNF93	cis	cerebellum	SCAN

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20112200-20148600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:20119000-20142200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr19:20119400-20148800	Weak transcription	Gastric	stomach
4	chr19:20119400-20149400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr19:20119600-20148000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:20119600-20149600	Weak transcription	Pancreas	Pancrea
7	chr19:20119800-20148000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr19:20120400-20149600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr19:20121400-20149200	Weak transcription	NHDF-Ad	bronchial
10	chr19:20125200-20149600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr19:20126000-20143000	Weak transcription	HSMM	muscle
12	chr19:20128800-20140800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr19:20129400-20149400	Weak transcription	Fetal Kidney	kidney
14	chr19:20130000-20148800	Weak transcription	Fetal Heart	heart
15	chr19:20130400-20149400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr19:20130400-20149400	Weak transcription	NHLF	lung
17	chr19:20130600-20141800	Weak transcription	Colonic Mucosa	Colon
18	chr19:20131600-20141600	Weak transcription	Psoas Muscle	Psoas
19	chr19:20131800-20141400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr19:20132400-20148800	Weak transcription	Spleen	Spleen
21	chr19:20133800-20143200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr19:20133800-20148800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr19:20133800-20149000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr19:20134000-20140800	Weak transcription	Primary T cells from cord blood	blood
25	chr19:20134000-20141600	Weak transcription	HSMMtube	muscle
26	chr19:20134000-20148800	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr19:20134000-20148800	Weak transcription	Brain Cingulate Gyrus	brain
28	chr19:20134000-20149200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr19:20134000-20149400	Weak transcription	Colon Smooth Muscle	Colon
30	chr19:20134000-20149600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr19:20134000-20149600	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr19:20134200-20140800	Weak transcription	Fetal Lung	lung
33	chr19:20134200-20141200	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr19:20134200-20141600	Weak transcription	Primary B cells from cord blood	blood
35	chr19:20134200-20144600	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr19:20134200-20148000	Weak transcription	Right Ventricle	heart
37	chr19:20134200-20148400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr19:20134200-20148400	Weak transcription	Aorta	Aorta
39	chr19:20134200-20148600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr19:20134200-20149000	Weak transcription	NHEK	skin
41	chr19:20134200-20149400	Weak transcription	Fetal Thymus	thymus
42	chr19:20134200-20149600	Weak transcription	Placenta	Placenta
43	chr19:20134600-20141200	Weak transcription	Fetal Intestine Small	intestine
44	chr19:20134600-20144200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr19:20134600-20148800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr19:20134600-20149400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:20134600-20149600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr19:20135000-20145000	Weak transcription	Osteobl	bone
49	chr19:20135200-20141800	Weak transcription	Fetal Brain Male	brain
50	chr19:20135200-20148400	Weak transcription	Primary T cells fromperipheralblood	blood

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