Variant report

Variant	nsv832056
Chromosome Location	chr11:4673001-4824890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:437)
CpG islands
(count:1038)
Chromatin interactive
region (count:44)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4679879-4680384	K562	blood:	n/a	n/a
2	ARID3A	chr11:4737623-4737722	K562	blood:	n/a	n/a
3	ATF1	chr11:4725319-4725444	K562	blood:	n/a	n/a
4	ATF1	chr11:4680154-4680354	K562	blood:	n/a	n/a
5	ATF1	chr11:4793218-4793283	K562	blood:	n/a	n/a
6	BATF	chr11:4720952-4721308	GM12878	blood:	n/a	chr11:4721121-4721132 chr11:4721122-4721132
7	BATF	chr11:4720966-4721312	GM12878	blood:	n/a	chr11:4721121-4721132 chr11:4721122-4721132
8	BHLHE40	chr11:4725569-4725710	K562	blood:	n/a	n/a
9	BHLHE40	chr11:4679927-4680079	K562	blood:	n/a	n/a
10	BHLHE40	chr11:4720909-4721365	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:4725424-4725706	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:4735655-4735881	K562	blood:	n/a	chr11:4735729-4735738 chr11:4735728-4735737 chr11:4735726-4735739 chr11:4735728-4735737 chr11:4735722-4735743
13	CBX3	chr11:4680009-4680493	K562	blood:	n/a	n/a
14	CCNT2	chr11:4766868-4767027	K562	blood:	n/a	n/a
15	CEBPB	chr11:4769720-4769999	K562	blood:	n/a	n/a
16	CEBPB	chr11:4811479-4811616	K562	blood:	n/a	n/a
17	CEBPB	chr11:4769725-4770036	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr11:4769715-4770029	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:4769714-4769970	A549	lung:	n/a	n/a
20	CEBPB	chr11:4802820-4802858	K562	blood:	n/a	chr11:4802839-4802852 chr11:4802839-4802852 chr11:4802841-4802852
21	CEBPB	chr11:4680108-4680438	K562	blood:	n/a	n/a
22	CEBPB	chr11:4727716-4727917	K562	blood:	n/a	n/a
23	CEBPB	chr11:4786195-4786260	HepG2	liver:	n/a	chr11:4786226-4786237
24	CEBPB	chr11:4680079-4680430	K562	blood:	n/a	n/a
25	CEBPB	chr11:4727964-4728051	A549	lung:	n/a	n/a
26	CEBPB	chr11:4678853-4679138	HepG2	liver:	n/a	chr11:4678998-4679009
27	CEBPB	chr11:4815769-4815953	K562	blood:	n/a	n/a
28	CEBPB	chr11:4718940-4719281	IMR90	lung:	n/a	chr11:4719120-4719133
29	CEBPB	chr11:4678840-4679165	K562	blood:	n/a	chr11:4678998-4679009
30	CEBPB	chr11:4779256-4779493	HepG2	liver:	n/a	chr11:4779363-4779374
31	CEBPB	chr11:4769682-4770051	IMR90	lung:	n/a	n/a
32	CEBPB	chr11:4696785-4696816	HepG2	liver:	n/a	n/a
33	CEBPD	chr11:4680058-4680601	K562	blood:	n/a	n/a
34	CHD1	chr11:4736940-4736955	GM12878	blood:	n/a	n/a
35	CHD2	chr11:4746213-4746346	K562	blood:	n/a	n/a
36	CHD2	chr11:4680006-4680343	K562	blood:	n/a	n/a
37	CHD2	chr11:4725736-4726172	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr11:4757393-4757648	K562	blood:	n/a	n/a
39	CTCF	chr11:4744166-4744322	A549	lung:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
40	CTCF	chr11:4804240-4804390	HEK293	kidney:	n/a	n/a
41	CTCF	chr11:4804220-4804370	GM06990	blood:	n/a	n/a
42	CTCF	chr11:4744158-4744326	GM19238	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
43	CTCF	chr11:4804240-4804390	GM06990	blood:	n/a	n/a
44	CTCF	chr11:4744111-4744374	H1-hESC	embryonic stem cell:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
45	CTCF	chr11:4807280-4807430	HEK293	kidney:	n/a	n/a
46	CTCF	chr11:4695380-4695530	HepG2	liver:	n/a	n/a
47	CTCF	chr11:4744157-4744340	MCF-7	breast:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
48	CTCF	chr11:4744120-4744270	K562	blood:	n/a	chr11:4744239-4744260 chr11:4744238-4744254 chr11:4744237-4744255
49	CTCF	chr11:4804246-4804395	GM12892	blood:	n/a	n/a
50	CTCF	chr11:4718960-4719110	AG04449	skin:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4704749-4704799	NT2-D1	testis:	n/a
2	chr11:4704749-4704799	NT2-D1	testis:	n/a
3	chr11:4719138-4719188	BJ	skin:	n/a
4	chr11:4824704-4824754	A549	lung:	n/a
5	chr11:4716867-4716917	NHBE	bronchial:	n/a
6	chr11:4674353-4674403	H1-hESC	embryonic stem cell:	embryo
7	chr11:4718962-4719012	HCT-116	colon:	n/a
8	chr11:4726105-4726155	K562	blood:	n/a
9	chr11:4791012-4791062	HIPEpiC	eye:	n/a
10	chr11:4703553-4703603	HIPEpiC	eye:	n/a
11	chr11:4674353-4674403	U87	brain:	n/a
12	chr11:4791012-4791062	T-47D	breast:	n/a
13	chr11:4674353-4674403	SAEC	small airway:	n/a
14	chr11:4704800-4704850	NB4	blood:	n/a
15	chr11:4726105-4726155	GM12891	blood:	n/a
16	chr11:4726105-4726155	SAEC	small airway:	n/a
17	chr11:4824704-4824754	ECC-1	luminal epithelium:	n/a
18	chr11:4719138-4719188	PrEC	prostate:	n/a
19	chr11:4693879-4693929	MCF-7	breast:	n/a
20	chr11:4824704-4824754	BJ	skin:	n/a
21	chr11:4676365-4676415	SKMC	muscle:	n/a
22	chr11:4704115-4704165	HEK293	kidney:	embryo
23	chr11:4718962-4719012	AoSMC	blood vessel:	n/a
24	chr11:4824704-4824754	H1-hESC	embryonic stem cell:	embryo
25	chr11:4704115-4704165	BJ	skin:	n/a
26	chr11:4824704-4824754	HEK293	kidney:	embryo
27	chr11:4720347-4720397	NT2-D1	testis:	n/a
28	chr11:4720347-4720397	GM06990	blood:	n/a
29	chr11:4674353-4674403	RPTEC	kidney:	n/a
30	chr11:4676365-4676415	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:4686966-4687016	IMR90	lung:	fetal
32	chr11:4718962-4719012	HRE	kidney:	n/a
33	chr11:4693879-4693929	HAEpiC	amniotic membrane:	n/a
34	chr11:4703553-4703603	Jurkat	blood:	n/a
35	chr11:4704115-4704165	HCPEpiC	choroid plexus:	n/a
36	chr11:4701824-4701874	Caco-2	colon:	n/a
37	chr11:4674353-4674403	GM19239	blood:	n/a
38	chr11:4719138-4719188	HNPCEpiC	eye:	n/a
39	chr11:4701824-4701874	HMEC	breast:	n/a
40	chr11:4693879-4693929	HMEC	breast:	n/a
41	chr11:4693879-4693929	BJ	skin:	n/a
42	chr11:4704800-4704850	IMR90	lung:	fetal
43	chr11:4704800-4704850	GM12878	blood:	n/a
44	chr11:4720347-4720397	AG04450	lung:	fetal
45	chr11:4718962-4719012	AG04449	skin:	fetal
46	chr11:4704115-4704165	K562	blood:	n/a
47	chr11:4719138-4719188	HUVEC	blood vessel:	n/a
48	chr11:4726105-4726155	NT2-D1	testis:	n/a
49	chr11:4693879-4693929	HepG2	liver:	n/a
50	chr11:4720347-4720397	GM19239	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:4817686..4819750-chr11:4821906..4823690,2	K562	blood:
2	11:4789513-4794705..11:4799792-4801044	GM12878	blood:
3	11:4794705-4799792..11:5527719-5533869	GM12878	blood:
4	chr11:4776926..4782057-chr11:4782402..4785593,4	K562	blood:
5	chr11:4671764..4674063-chr11:4698121..4699721,2	K562	blood:
6	11:4789513-4794705..11:5033143-5038367	K562	blood:
7	chr11:4758799..4760631-chr11:4763154..4765476,2	K562	blood:
8	chr11:4806483..4808284-chr11:4810226..4812694,2	K562	blood:
9	chr11:4676620..4679350-chr11:4683230..4685666,3	K562	blood:
10	11:4789513-4794705..11:5380014-5384338	H1-hESC	embryonic stem cell:	embryo
11	chr11:4780407..4782336-chr11:4786292..4788948,2	K562	blood:
12	11:4794705-4799792..11:5721056-5732713	K562	blood:
13	chr11:4677690..4682058-chr11:4682699..4685666,4	K562	blood:
14	11:4778081-4789138..11:5033143-5038367	K562	blood:
15	chr11:4789671..4792092-chr11:4812812..4815235,2	K562	blood:
16	11:4820112-4824892..11:5700314-5707362	K562	blood:
17	chr11:4817686..4819750-chr11:4821906..4823690,2	K562	blood:
18	chr11:4769802..4772330-chr11:4775914..4778474,2	K562	blood:
19	11:4774420-4775061..11:5527719-5533869	GM12878	blood:
20	chr11:4758799..4760631-chr11:4763154..4765476,2	K562	blood:
21	11:4801044-4820112..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
22	11:4774420-4775061..11:5250847-5268367	GM12878	blood:
23	11:4778081-4789138..11:5740069-5747001	K562	blood:
24	chr11:4688697..4691190-chr11:4691672..4693874,2	K562	blood:
25	chr11:4667581..4670496-chr11:4674502..4676349,2	K562	blood:
26	chr11:4778466..4780961-chr11:4783951..4785593,2	K562	blood:
27	11:4820112-4824892..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
28	chr11:4779685..4780186-chr13:39427810..39428310,2	MCF-7	breast:
29	11:4820112-4824892..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
30	chr11:4747857..4749971-chr11:4751424..4753265,2	K562	blood:
31	11:4774420-4775061..11:5714465-5718134	GM12878	blood:
32	chr11:4747857..4749971-chr11:4751424..4753265,2	K562	blood:
33	11:4778081-4789138..11:4988858-5002113	Hela-S3	cervix:
34	11:4794705-4799792..11:5714465-5718134	H1-hESC	embryonic stem cell:	embryo
35	chr11:4688697..4691190-chr11:4691672..4693874,2	K562	blood:
36	chr11:4785049..4787150-chr11:4787794..4789663,2	K562	blood:
37	chr11:4778466..4780961-chr11:4783951..4785593,2	K562	blood:
38	chr11:4783931..4787132-chr11:4790389..4793666,3	K562	blood:
39	chr11:4676620..4679350-chr11:4683230..4685666,3	K562	blood:
40	chr11:4706166..4708842-chr11:4710563..4713479,3	K562	blood:
41	11:4820112-4824892..11:5018576-5020673	H1-hESC	embryonic stem cell:	embryo
42	11:4794705-4799792..11:5700314-5707362	K562	blood:
43	11:4789513-4794705..11:4988858-5002113	Hela-S3	cervix:
44	chr11:4716790..4717429-chr5:66479554..66480313,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51E1-1	chr11:4693251-4693545	NONHSAT017652
2	lnc-OR51E1-1	chr11:4687857-4688192	XLOC_009038
3	lnc-OR51E1-1	chr11:4690901-4691087	XLOC_009038
4	lnc-OR51E1-1	chr11:4687857-4688192	XLOC_009038
5	lnc-OR51E1-1	chr11:4693251-4693462	XLOC_009038
6	lnc-OR51E1-1	chr11:4693251-4693464	XLOC_009038
7	lnc-OR52R1-1	chr11:4816146-4816514	NONHSAT017656
8	lnc-MMP26-1	chr11:4788500-4788571	NONHSAT017654
9	lnc-OR51E1-1	chr11:4687857-4688192	NONHSAT017652
10	lnc-MMP26-1	chr11:4726157-4726275	NONHSAT017654
11	lnc-OR52R1-1	chr11:4815008-4815466	NONHSAT017656

No data

Variant related genes	Relation type
OR51N1P	TF binding region
OR51E1	TF binding region
ENSG00000201980	TF binding region
OR51F1	TF binding region
OR51C1P	TF binding region
OR51F5P	TF binding region
KRT8P49	TF binding region
OR51C4P	TF binding region
OR51F3P	TF binding region
OR52Y1P	TF binding region
OR51E2	TF binding region
OR51A9P	TF binding region
MMP26	TF binding region
OR51F4P	TF binding region
OR51N1P	CpG island
OR51E1	CpG island
ENSG00000201980	CpG island
OR51F1	CpG island
OR51C1P	CpG island
OR51F5P	CpG island
KRT8P49	CpG island
OR51C4P	CpG island
OR51F3P	CpG island
OR52Y1P	CpG island
OR51E2	CpG island
OR51A9P	CpG island
MMP26	CpG island
OR51F4P	CpG island
ENSG00000229988	chromatin interactions
ENSG00000180785	chromatin interactions
ENSG00000232381	chromatin interactions
ENSG00000236248	chromatin interactions
ENSG00000188069	chromatin interactions
ENSG00000201980	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000180723	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000176798	chromatin interactions
ENSG00000176951	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000197674	chromatin interactions
ENSG00000167346	chromatin interactions

Extended variants
information (count: 5410 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:5410 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12283337	chr11:4673007-4673008	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558313310	chr11:4673074-4673075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566870947	chr11:4673083-4673084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534224507	chr11:4673084-4673085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12280089	chr11:4673106-4673107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs149091278	chr11:4673119-4673120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79032420	chr11:4673136-4673137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187970851	chr11:4673155-4673156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79122020	chr11:4673221-4673222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192918019	chr11:4673225-4673226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559859958	chr11:4673326-4673327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544205874	chr11:4673345-4673346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542171537	chr11:4673359-4673360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182071597	chr11:4673395-4673396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531602907	chr11:4673404-4673405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549842061	chr11:4673448-4673449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34514339	chr11:4673518-4673519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571399105	chr11:4673552-4673553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563879437	chr11:4673624-4673625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4910524	chr11:4673647-4673648	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs547086307	chr11:4673653-4673654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551896962	chr11:4673660-4673661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138939346	chr11:4673661-4673662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534289904	chr11:4673697-4673698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555704272	chr11:4673699-4673700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567567972	chr11:4673701-4673702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186702383	chr11:4673711-4673712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369401438	chr11:4673747-4673748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199976122	chr11:4673749-4673750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149764012	chr11:4673773-4673774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146791038	chr11:4673774-4673775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17224476	chr11:4673788-4673789	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs145680929	chr11:4673794-4673795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372848649	chr11:4673829-4673830	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142883708	chr11:4673832-4673833	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201014805	chr11:4673848-4673849	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146592303	chr11:4673871-4673872	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs202046967	chr11:4673878-4673879	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146943434	chr11:4673893-4673894	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374881313	chr11:4673896-4673897	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200858824	chr11:4673913-4673914	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199983119	chr11:4673914-4673915	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567104163	chr11:4673933-4673934	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560924436	chr11:4673965-4673966	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149084031	chr11:4673974-4673975	Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190765812	chr11:4674016-4674017	Weak transcription Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372544700	chr11:4674083-4674084	Weak transcription Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200393599	chr11:4674128-4674129	Weak transcription Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200807047	chr11:4674129-4674130	Weak transcription Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192878981	chr11:4674157-4674158	Weak transcription Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4665400-4677000	Weak transcription	Spleen	Spleen
2	chr11:4665800-4686600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:4669400-4674200	Weak transcription	Right Ventricle	heart
4	chr11:4669600-4680400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr11:4670000-4676200	Weak transcription	Adipose Nuclei	Adipose
6	chr11:4670800-4673800	Weak transcription	Ovary	ovary
7	chr11:4673000-4673800	Weak transcription	Left Ventricle	heart
8	chr11:4673800-4674000	Bivalent/Poised TSS	Brain Substantia Nigra	brain
9	chr11:4673800-4674600	Genic enhancers	Left Ventricle	heart
10	chr11:4673800-4674600	Strong transcription	Ovary	ovary
11	chr11:4674000-4674400	Active TSS	Brain Substantia Nigra	brain
12	chr11:4674600-4678200	Weak transcription	Left Ventricle	heart
13	chr11:4674600-4679800	Weak transcription	Ovary	ovary
14	chr11:4678800-4679400	Enhancers	K562	blood
15	chr11:4679000-4680800	Enhancers	Fetal Heart	heart
16	chr11:4679400-4680200	Flanking Active TSS	K562	blood
17	chr11:4679400-4680800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:4679800-4680000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr11:4679800-4680600	Enhancers	Ovary	ovary
20	chr11:4679800-4680800	Enhancers	Fetal Kidney	kidney
21	chr11:4680000-4680600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:4680000-4680800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr11:4680200-4680600	Active TSS	K562	blood
24	chr11:4680400-4680600	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr11:4680400-4680800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr11:4680600-4680800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr11:4680600-4680800	Flanking Active TSS	K562	blood
28	chr11:4680600-4682000	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr11:4680800-4681600	Enhancers	K562	blood
30	chr11:4680800-4684600	Weak transcription	Fetal Heart	heart
31	chr11:4684600-4685200	Enhancers	Fetal Heart	heart
32	chr11:4685200-4693000	Weak transcription	Fetal Heart	heart
33	chr11:4687000-4687600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:4692200-4692400	Enhancers	NHLF	lung
35	chr11:4692200-4693200	Enhancers	Ovary	ovary
36	chr11:4692400-4694000	Weak transcription	NHLF	lung
37	chr11:4692400-4694400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:4693000-4693400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr11:4693000-4693400	Enhancers	Fetal Muscle Leg	muscle
40	chr11:4693000-4693600	Enhancers	Adipose Nuclei	Adipose
41	chr11:4693000-4694600	Enhancers	Fetal Heart	heart
42	chr11:4693200-4693600	Enhancers	Brain Germinal Matrix	brain
43	chr11:4693200-4694000	Weak transcription	Ovary	ovary
44	chr11:4693200-4694600	Enhancers	HSMMtube	muscle
45	chr11:4693200-4696000	Enhancers	NHDF-Ad	bronchial
46	chr11:4693400-4693600	Enhancers	Fetal Kidney	kidney
47	chr11:4693400-4693800	Weak transcription	Fetal Muscle Leg	muscle
48	chr11:4693400-4694200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:4693400-4694400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr11:4693400-4694400	Enhancers	HSMM	muscle

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