Variant report

Variant	rs11085431
Chromosome Location	chr19:21306913-21306914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF714-2	chr19:21306620-21306991	NONHSAT063687

Extended variants
information (count: 169 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:152)

rs_ID	r²[population]
rs10164375	0.89[ASN][1000 genomes]
rs10401931	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10403266	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10405180	1.00[ASN][1000 genomes]
rs10405218	0.88[ASN][1000 genomes]
rs10405406	0.94[ASN][1000 genomes]
rs10406661	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[YRI][hapmap];0.89[ASN][1000 genomes]
rs10408496	0.81[JPT][hapmap]
rs10409844	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10409877	1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[ASN][1000 genomes]
rs10410901	1.00[CHB][hapmap];0.91[JPT][hapmap];0.94[ASN][1000 genomes]
rs10411038	0.94[ASN][1000 genomes]
rs10412267	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[YRI][hapmap];0.91[ASN][1000 genomes]
rs10412509	0.80[CHD][hapmap];0.94[JPT][hapmap];0.93[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10412688	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10413175	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10413692	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10413983	0.91[ASN][1000 genomes]
rs10414134	0.91[ASN][1000 genomes]
rs10417165	0.82[ASN][1000 genomes]
rs10421819	0.89[ASN][1000 genomes]
rs10423541	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.98[ASN][1000 genomes]
rs10424283	0.91[ASN][1000 genomes]
rs10425969	0.88[ASN][1000 genomes]
rs11085424	0.82[ASN][1000 genomes]
rs11085429	0.83[CEU][hapmap]
rs11666640	0.88[ASN][1000 genomes]
rs11666869	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11667674	0.97[ASN][1000 genomes]
rs11668952	0.97[ASN][1000 genomes]
rs11668985	0.95[ASN][1000 genomes]
rs11669248	0.98[EUR][1000 genomes]
rs11670162	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11671397	0.97[ASN][1000 genomes]
rs11672142	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11672727	0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11672747	0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11878599	0.97[ASN][1000 genomes]
rs12052091	0.83[CEU][hapmap]
rs12104220	0.91[ASN][1000 genomes]
rs12608706	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12608931	0.89[EUR][1000 genomes]
rs12609005	0.88[ASN][1000 genomes]
rs12609167	0.89[CEU][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12609427	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12609831	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12611115	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12973640	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12973921	0.97[ASN][1000 genomes]
rs12974016	0.94[ASN][1000 genomes]
rs12975789	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12976796	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12981855	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1470021	0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1470022	0.97[ASN][1000 genomes]
rs1609441	0.86[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1968523	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1975056	0.83[CEU][hapmap]
rs2013048	0.91[ASN][1000 genomes]
rs2081050	0.80[ASN][1000 genomes]
rs2081055	0.85[EUR][1000 genomes]
rs2081056	0.85[EUR][1000 genomes]
rs2082003	0.91[ASN][1000 genomes]
rs2098681	0.80[ASN][1000 genomes]
rs2112803	0.89[EUR][1000 genomes]
rs2115493	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[ASN][1000 genomes]
rs2115494	0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2115495	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2115496	0.94[JPT][hapmap]
rs2164988	0.83[ASN][1000 genomes]
rs2164989	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2195453	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2195454	0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2358792	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2358795	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2358803	0.97[ASN][1000 genomes]
rs2358804	0.97[ASN][1000 genomes]
rs2884554	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34726293	0.80[EUR][1000 genomes]
rs35137761	0.94[ASN][1000 genomes]
rs4292035	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4365405	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4488591	0.86[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs4808275	0.94[ASN][1000 genomes]
rs4808276	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4809119	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4809122	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.80[YRI][hapmap];0.97[ASN][1000 genomes]
rs62122564	0.85[EUR][1000 genomes]
rs62122565	0.85[EUR][1000 genomes]
rs6511179	0.89[EUR][1000 genomes]
rs6511181	0.80[ASN][1000 genomes]
rs6511183	0.88[ASN][1000 genomes]
rs6511184	0.88[ASN][1000 genomes]
rs6511186	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6511187	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6511188	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6511190	0.83[ASN][1000 genomes]
rs6511191	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6511192	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[ASN][1000 genomes]
rs6511194	0.85[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs6511195	0.86[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6511196	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6511198	0.97[ASN][1000 genomes]
rs6511199	0.97[ASN][1000 genomes]
rs6511200	0.97[ASN][1000 genomes]
rs6511201	0.97[ASN][1000 genomes]
rs7246723	1.00[JPT][hapmap];0.86[YRI][hapmap];0.91[ASN][1000 genomes]
rs7247413	0.82[ASN][1000 genomes]
rs7248087	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7248410	0.94[ASN][1000 genomes]
rs7249283	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7249736	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7250169	0.91[ASN][1000 genomes]
rs7252277	0.82[ASN][1000 genomes]
rs7253530	0.82[ASN][1000 genomes]
rs7253950	0.97[ASN][1000 genomes]
rs7254047	0.86[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7254053	0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs7254982	0.89[ASN][1000 genomes]
rs7257481	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7258195	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7258409	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7258831	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7260268	0.86[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7260600	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7343175	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs741674	0.97[ASN][1000 genomes]
rs741676	0.97[ASN][1000 genomes]
rs8100289	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8100599	0.91[ASN][1000 genomes]
rs8101222	1.00[ASN][1000 genomes]
rs8101412	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8101461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8103696	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8103825	0.94[ASN][1000 genomes]
rs8106801	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs8106923	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[ASN][1000 genomes]
rs8107638	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8107982	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8109549	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8109577	0.81[EUR][1000 genomes]
rs8111827	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.80[YRI][hapmap];1.00[ASN][1000 genomes]
rs8112054	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs8112216	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8112500	0.94[ASN][1000 genomes]
rs8113541	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs8182465	0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs9304980	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9304981	0.93[JPT][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9304982	1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[ASN][1000 genomes]
rs9941463	0.82[ASN][1000 genomes]
rs9967619	0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3385528	chr19:21030777-21495566	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv817536	chr19:21041855-21348237	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv960811	chr19:21200306-21371757	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	esv3399352	chr19:21232738-21423323	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv1065384	chr19:21249321-21350698	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv911413	chr19:21263518-21347598	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	esv3319019	chr19:21268262-21336383	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	esv3319020	chr19:21268262-21336383	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	esv7695	chr19:21268276-21328430	Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
10	esv5909	chr19:21272333-21334753	Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
11	esv3420290	chr19:21272477-21336432	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
12	esv3391713	chr19:21272485-21334631	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
13	esv5243	chr19:21272548-21334670	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
14	esv7204	chr19:21274198-21336396	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
15	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
16	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
17	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs11085431	ZNF429	cis	cerebellum	SCAN
rs11085431	ZNF714	cis	parietal	SCAN
rs11085431	ZNF714	cis	Nerve Tibial	GTEx
rs11085431	ZNF714	cis	cerebellum	SCAN
rs11085431	ZNF681	cis	cerebellum	SCAN
rs11085431	RFXANK	cis	cerebellum	SCAN
rs11085431	ZNF100	cis	cerebellum	SCAN
rs11085431	MYO9B	cis	cerebellum	SCAN
rs11085431	ZNF737	cis	parietal	SCAN
rs11085431	ZNF429	cis	multi-tissue	Pritchard
rs11085431	ZNF429	cis	parietal	SCAN

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21291600-21307800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr19:21297600-21310600	Weak transcription	HepG2	liver
3	chr19:21297800-21311200	Weak transcription	Right Ventricle	heart
4	chr19:21300400-21311600	Weak transcription	Fetal Kidney	kidney
5	chr19:21300600-21309600	Weak transcription	K562	blood
6	chr19:21300600-21310600	Weak transcription	Fetal Intestine Large	intestine
7	chr19:21301000-21311800	Weak transcription	Ovary	ovary
8	chr19:21301200-21310800	Weak transcription	Primary T cells from cord blood	blood
9	chr19:21301200-21311800	Weak transcription	Fetal Thymus	thymus
10	chr19:21301800-21307000	Weak transcription	Osteobl	bone
11	chr19:21302200-21307000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr19:21302200-21307000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr19:21302200-21309400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr19:21302200-21310400	Weak transcription	Esophagus	oesophagus
15	chr19:21302400-21308600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr19:21302400-21312200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr19:21303000-21311600	Weak transcription	Dnd41	blood
18	chr19:21303200-21309800	Weak transcription	Fetal Stomach	stomach
19	chr19:21303200-21310800	Weak transcription	Thymus	Thymus
20	chr19:21303200-21311200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr19:21303200-21311800	Weak transcription	Fetal Intestine Small	intestine
22	chr19:21303200-21312000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr19:21303200-21312600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr19:21303400-21311200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr19:21303800-21311600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:21304000-21308400	Weak transcription	Fetal Brain Female	brain
27	chr19:21304200-21313000	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr19:21305400-21311000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr19:21305400-21311200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr19:21305600-21309600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr19:21305600-21312000	Weak transcription	Fetal Lung	lung
32	chr19:21305600-21312200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr19:21305800-21307400	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr19:21305800-21307600	Weak transcription	Fetal Muscle Leg	muscle
35	chr19:21305800-21309400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr19:21305800-21313000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr19:21305800-21313000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr19:21306000-21308600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr19:21306000-21310600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr19:21306000-21311200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr19:21306600-21307000	ZNF genes & repeats	A549	lung
42	chr19:21306800-21307000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr19:21306800-21307000	Enhancers	NH-A	brain
44	chr19:21306800-21307000	Enhancers	NHEK	skin
45	chr19:21306800-21307400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr19:21306800-21307400	Enhancers	HSMM	muscle

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