Variant report

Variant	esv3527908
Chromosome Location	chr3:43327298-43329521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:43327766-43327832	K562	blood:	n/a	n/a
2	ARID3A	chr3:43327734-43328196	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:43328109-43328122	K562	blood:	n/a	n/a
4	ATF1	chr3:43327620-43328180	K562	blood:	n/a	n/a
5	ATF3	chr3:43327879-43328116	K562	blood:	n/a	chr3:43327994-43328009 chr3:43327998-43328008 chr3:43327995-43328008 chr3:43327995-43328005 chr3:43327998-43328005 chr3:43327995-43328006 chr3:43327996-43328007 chr3:43327998-43328006 chr3:43327996-43328007 chr3:43327995-43328008 chr3:43327995-43328005 chr3:43327994-43328007 chr3:43327998-43328008
6	BHLHE40	chr3:43327568-43328118	K562	blood:	n/a	chr3:43328051-43328067 chr3:43328052-43328068
7	BHLHE40	chr3:43327317-43327927	HepG2	liver:	n/a	n/a
8	BHLHE40	chr3:43327636-43328158	GM12878	blood:	n/a	chr3:43328124-43328140 chr3:43328135-43328151 chr3:43328051-43328067 chr3:43328127-43328143 chr3:43328126-43328142 chr3:43328052-43328068
9	BRCA1	chr3:43328162-43328165	HepG2	liver:	n/a	n/a
10	BRCA1	chr3:43327652-43328018	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr3:43327625-43328173	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr3:43327511-43327953	K562	blood:	n/a	n/a
13	CCNT2	chr3:43327739-43328725	K562	blood:	n/a	n/a
14	CEBPB	chr3:43328384-43328614	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:43328472-43328608	K562	blood:	n/a	n/a
16	CEBPB	chr3:43327764-43328102	Hela-S3	cervix:	n/a	n/a
17	CEBPD	chr3:43327798-43328232	HepG2	liver:	n/a	n/a
18	CHD1	chr3:43328730-43328891	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr3:43327287-43327662	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr3:43328042-43328280	GM12878	blood:	n/a	n/a
21	CHD2	chr3:43327719-43328208	K562	blood:	n/a	chr3:43327825-43327835
22	CHD2	chr3:43327720-43328117	HepG2	liver:	n/a	chr3:43327825-43327835
23	CHD2	chr3:43328658-43328779	K562	blood:	n/a	n/a
24	CHD2	chr3:43327330-43328199	Hela-S3	cervix:	n/a	chr3:43327825-43327835
25	CHD2	chr3:43327647-43327901	H1-hESC	embryonic stem cell:	n/a	chr3:43327825-43327835
26	CHD2	chr3:43327658-43328189	GM12878	blood:	n/a	chr3:43327825-43327835
27	CREB1	chr3:43327641-43328303	K562	blood:	n/a	chr3:43327995-43328008
28	CREB1	chr3:43327461-43328353	K562	blood:	n/a	chr3:43327995-43328008
29	CREB1	chr3:43327820-43328186	A549	lung:	n/a	chr3:43327995-43328008
30	CREB1	chr3:43327620-43328342	A549	lung:	n/a	chr3:43327995-43328008
31	CREB1	chr3:43327804-43328145	ECC-1	luminal epithelium:	n/a	chr3:43327995-43328008
32	CREB1	chr3:43327816-43328162	ECC-1	luminal epithelium:	n/a	chr3:43327995-43328008
33	CREB1	chr3:43327583-43328333	HepG2	liver:	n/a	chr3:43327995-43328008
34	CREB1	chr3:43327614-43328307	HepG2	liver:	n/a	chr3:43327995-43328008
35	CREB1	chr3:43327634-43328339	GM12878	blood:	n/a	chr3:43327995-43328008
36	CREB1	chr3:43327639-43328294	H1-hESC	embryonic stem cell:	n/a	chr3:43327995-43328008
37	CREB1	chr3:43327555-43328312	H1-hESC	embryonic stem cell:	n/a	chr3:43327995-43328008
38	CREB1	chr3:43327526-43328311	GM12878	blood:	n/a	chr3:43327995-43328008
39	CTCF	chr3:43327640-43327790	HEEpiC	esophagus:	n/a	chr3:43327712-43327725
40	CTCF	chr3:43327679-43327817	GM10248	blood:	n/a	chr3:43327712-43327725
41	CTCF	chr3:43327620-43327770	AG09309	skin:	n/a	chr3:43327712-43327725
42	CTCF	chr3:43327500-43327650	A549	lung:	n/a	n/a
43	CTCF	chr3:43327540-43327690	AG04450	lung:	n/a	n/a
44	CTCF	chr3:43327680-43327830	HPAF	blood vessel:	n/a	chr3:43327712-43327725
45	CTCF	chr3:43327640-43327790	AG10803	skin:	n/a	chr3:43327712-43327725
46	CTCF	chr3:43327655-43327809	K562	blood:	n/a	chr3:43327712-43327725
47	CTCF	chr3:43327655-43327853	GM12891	blood:	n/a	chr3:43327712-43327725
48	CTCF	chr3:43327700-43327850	Hela-S3	cervix:	n/a	chr3:43327712-43327725
49	CTCF	chr3:43328680-43328830	K562	blood:	n/a	n/a
50	CTCF	chr3:43327640-43327790	GM12874	blood:	n/a	chr3:43327712-43327725

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:43327362-43327412	AG09319	gingival:	n/a
2	chr3:43327699-43327749	SK-N-SH_RA	brain:	n/a
3	chr3:43327362-43327412	NH-A	brain:	n/a
4	chr3:43328001-43328051	U87	brain:	n/a
5	chr3:43327880-43327930	NHBE	bronchial:	n/a
6	chr3:43328001-43328051	PrEC	prostate:	n/a
7	chr3:43327880-43327930	AG10803	skin:	n/a
8	chr3:43327880-43327930	A549	lung:	n/a
9	chr3:43327880-43327930	NT2-D1	testis:	n/a
10	chr3:43328001-43328051	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:43328001-43328051	BJ	skin:	n/a
12	chr3:43327465-43327515	MCF-7	breast:	n/a
13	chr3:43327465-43327515	PFSK-1	brain:	n/a
14	chr3:43327362-43327412	HCPEpiC	choroid plexus:	n/a
15	chr3:43327362-43327412	ECC-1	luminal epithelium:	n/a
16	chr3:43328001-43328051	HCM	heart:	n/a
17	chr3:43327880-43327930	AG09319	gingival:	n/a
18	chr3:43327699-43327749	A549	lung:	n/a
19	chr3:43327880-43327930	HMEC	breast:	n/a
20	chr3:43328001-43328051	T-47D	breast:	n/a
21	chr3:43328001-43328051	NH-A	brain:	n/a
22	chr3:43327699-43327749	MCF-7	breast:	n/a
23	chr3:43327465-43327515	NHBE	bronchial:	n/a
24	chr3:43327362-43327412	LNCaP	prostate:	n/a
25	chr3:43327880-43327930	RPTEC	kidney:	n/a
26	chr3:43327465-43327515	RPTEC	kidney:	n/a
27	chr3:43327362-43327412	HNPCEpiC	eye:	n/a
28	chr3:43327465-43327515	NH-A	brain:	n/a
29	chr3:43327699-43327749	AG10803	skin:	n/a
30	chr3:43327699-43327749	MCF10A-Er-Src	breast:	n/a
31	chr3:43327465-43327515	CMK	blood:	n/a
32	chr3:43327362-43327412	GM12878	blood:	n/a
33	chr3:43327362-43327412	SAEC	small airway:	n/a
34	chr3:43327465-43327515	HNPCEpiC	eye:	n/a
35	chr3:43327362-43327412	T-47D	breast:	n/a
36	chr3:43328001-43328051	ovcar-3	ovarian:	n/a
37	chr3:43327362-43327412	HMEC	breast:	n/a
38	chr3:43327699-43327749	HRE	kidney:	n/a
39	chr3:43327699-43327749	PFSK-1	brain:	n/a
40	chr3:43327465-43327515	AG10803	skin:	n/a
41	chr3:43327362-43327412	HEK293	kidney:	embryo
42	chr3:43327880-43327930	NH-A	brain:	n/a
43	chr3:43327465-43327515	SAEC	small airway:	n/a
44	chr3:43328001-43328051	RPTEC	kidney:	n/a
45	chr3:43327880-43327930	Hepatocyte	liver:	n/a
46	chr3:43327699-43327749	Hela-S3	cervix:	n/a
47	chr3:43327699-43327749	H1-hESC	embryonic stem cell:	embryo
48	chr3:43327699-43327749	ECC-1	luminal epithelium:	n/a
49	chr3:43327362-43327412	HCM	heart:	n/a
50	chr3:43327880-43327930	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:1249504..1250049-chr3:43327521..43328330,2	Hela-S3	cervix:
2	chr3:43327640..43330625-chr3:43731199..43733951,3	K562	blood:
3	chr3:43327783..43328333-chr5:32173796..32174464,2	Hela-S3	cervix:
4	chr3:43320796..43322949-chr3:43328990..43330664,2	K562	blood:
5	chr3:43305979..43308043-chr3:43325669..43327950,2	MCF-7	breast:
6	chr3:43328576..43330209-chr3:43363736..43365348,2	K562	blood:
7	chr2:208394589..208395128-chr3:43327696..43328487,2	Hela-S3	cervix:
8	chr20:30192245..30193126-chr3:43327692..43328283,2	Hela-S3	cervix:
9	chr10:98346013..98346591-chr3:43327414..43328126,2	Hela-S3	cervix:
10	chr3:43325116..43327718-chr3:43329418..43331490,2	K562	blood:
11	chr3:43325116..43327718-chr3:43329418..43331490,2	K562	blood:
12	chr3:43314193..43316141-chr3:43325214..43327876,2	K562	blood:
13	chr3:43328082..43330424-chr3:43353703..43355564,2	K562	blood:
14	chr3:43328459..43331117-chr3:43356191..43358697,2	K562	blood:
15	chr14:103988769..103989622-chr3:43327887..43328473,2	HCT-116	colon:
16	chr3:43328259..43329793-chr3:43345734..43348023,2	K562	blood:

Variant related genes	Relation type
SNRK	TF binding region
SNRK	CpG island
ENSG00000113384	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000166165	chromatin interactions
ENSG00000167470	chromatin interactions
ENSG00000160746	chromatin interactions
ENSG00000011198	chromatin interactions
ENSG00000241939	chromatin interactions
ENSG00000118260	chromatin interactions
ENSG00000077147	chromatin interactions

Extended variants
information (count: 61 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:61 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574615932	chr3:43327338-43327339	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs73831234	chr3:43327343-43327344	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs559914489	chr3:43327358-43327359	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374755897	chr3:43327375-43327376	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs538317724	chr3:43327437-43327438	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545687845	chr3:43327439-43327440	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs565486878	chr3:43327503-43327504	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531100786	chr3:43327610-43327611	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs575422236	chr3:43327652-43327653	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs538439055	chr3:43327688-43327689	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs145900249	chr3:43327714-43327715	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs560918933	chr3:43327725-43327726	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs187439730	chr3:43327773-43327774	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs530147883	chr3:43327821-43327822	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs368350776	chr3:43327853-43327854	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs546737141	chr3:43327907-43327908	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs566660290	chr3:43327909-43327910	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs532252766	chr3:43327918-43327919	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs552336473	chr3:43327943-43327944	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs569206949	chr3:43327944-43327945	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs538118772	chr3:43327994-43327995	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs554630421	chr3:43327995-43327996	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs568026651	chr3:43328014-43328015	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs148185233	chr3:43328044-43328045	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs553541262	chr3:43328057-43328058	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs372569196	chr3:43328064-43328065	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs545317748	chr3:43328082-43328083	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs559092205	chr3:43328085-43328086	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs141210890	chr3:43328116-43328117	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs113426625	chr3:43328138-43328139	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs35392864	chr3:43328219-43328220	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs544469305	chr3:43328239-43328240	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs560955633	chr3:43328289-43328290	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs529989541	chr3:43328616-43328617	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs540617267	chr3:43328637-43328638	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs377219137	chr3:43328639-43328640	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs560419981	chr3:43328666-43328667	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs114541130	chr3:43328670-43328671	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs150311589	chr3:43328695-43328696	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs569047198	chr3:43328696-43328697	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs58866653	chr3:43328758-43328759	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548466842	chr3:43328798-43328799	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs138158411	chr3:43328813-43328814	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs143620204	chr3:43328912-43328913	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs1506618	chr3:43328946-43328947	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570488141	chr3:43328999-43329000	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs13069409	chr3:43329013-43329014	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs572315542	chr3:43329072-43329073	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs558742075	chr3:43329077-43329078	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs575390780	chr3:43329100-43329101	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Wilms tumour	17204608	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Kartagener syndrome	16639409	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43318800-43327800	Weak transcription	Small Intestine	intestine
2	chr3:43325200-43327400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr3:43326200-43327400	Enhancers	Fetal Brain Male	brain
4	chr3:43326400-43327400	Enhancers	Adipose Nuclei	Adipose
5	chr3:43326400-43327600	Enhancers	HUVEC	blood vessel
6	chr3:43326600-43327400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr3:43326600-43327400	Enhancers	Thymus	Thymus
8	chr3:43326800-43327400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
9	chr3:43326800-43327600	Enhancers	Fetal Thymus	thymus
10	chr3:43326800-43327600	Enhancers	Spleen	Spleen
11	chr3:43327000-43327400	Enhancers	Fetal Stomach	stomach
12	chr3:43327000-43327400	Enhancers	Psoas Muscle	Psoas
13	chr3:43327000-43327400	Enhancers	Stomach Smooth Muscle	stomach
14	chr3:43327000-43327400	Flanking Bivalent TSS/Enh	HepG2	liver
15	chr3:43327000-43327600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr3:43327000-43327600	Enhancers	Esophagus	oesophagus
17	chr3:43327000-43327600	Enhancers	Fetal Muscle Leg	muscle
18	chr3:43327000-43327600	Enhancers	Left Ventricle	heart
19	chr3:43327000-43327600	Enhancers	Right Ventricle	heart
20	chr3:43327000-43327600	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr3:43327000-43327600	Enhancers	Stomach Mucosa	stomach
22	chr3:43327200-43327400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
23	chr3:43327200-43327400	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr3:43327200-43327400	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:43327200-43327400	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:43327200-43327400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:43327200-43327400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr3:43327200-43327400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr3:43327200-43327400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr3:43327200-43327400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr3:43327200-43327400	Enhancers	Primary B cells from cord blood	blood
32	chr3:43327200-43327400	Enhancers	Primary B cells from peripheral blood	blood
33	chr3:43327200-43327400	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr3:43327200-43327400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr3:43327200-43327400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr3:43327200-43327400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:43327200-43327400	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr3:43327200-43327400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr3:43327200-43327400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr3:43327200-43327400	Enhancers	Brain Anterior Caudate	brain
41	chr3:43327200-43327400	Flanking Active TSS	Lung	lung
42	chr3:43327200-43327400	Enhancers	K562	blood
43	chr3:43327200-43327400	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr3:43327200-43327400	Enhancers	NHEK	skin
45	chr3:43327200-43327400	Bivalent Enhancer	Osteobl	bone
46	chr3:43327200-43327600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
47	chr3:43327200-43327600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr3:43327200-43327600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
49	chr3:43327200-43327600	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr3:43327200-43327600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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