Variant report

Variant	esv3403870
Chromosome Location	chr3:51740262-51741860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:210)
CpG islands
(count:428)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:210 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:51740735-51741003	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:51740809-51741013	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr3:51740768-51740996	K562	blood:	n/a	n/a
4	CEBPD	chr3:51740798-51740998	HepG2	liver:	n/a	n/a
5	CHD2	chr3:51740871-51740973	HepG2	liver:	n/a	n/a
6	CHD2	chr3:51740767-51741059	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr3:51740786-51741151	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr3:51740840-51740990	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr3:51740800-51740950	BJ	skin:	n/a	n/a
10	CTCF	chr3:51740820-51740970	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr3:51740840-51740990	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr3:51740911-51740966	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr3:51740840-51740990	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr3:51740849-51740970	Pancreas_OC	pancreas:	n/a	n/a
15	CTCF	chr3:51740840-51740990	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr3:51740820-51740970	Caco-2	colon:	n/a	n/a
17	CTCF	chr3:51740860-51741010	HMEC	breast:	n/a	n/a
18	CTCF	chr3:51740801-51740984	IMR90	lung:	n/a	n/a
19	CTCF	chr3:51740893-51740958	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr3:51740820-51740970	AG04450	lung:	n/a	n/a
21	CTCF	chr3:51740860-51741010	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr3:51740860-51741010	HMF	breast:	n/a	n/a
23	CTCF	chr3:51740840-51740990	SAEC	small airway:	n/a	n/a
24	CTCF	chr3:51740820-51740970	HAc	cerebellar:	n/a	n/a
25	CTCF	chr3:51740840-51740990	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr3:51740840-51740990	HPF	lung:	n/a	n/a
27	CTCF	chr3:51740820-51740970	AG09319	gingival:	n/a	n/a
28	CTCF	chr3:51740840-51740990	HCFaa	heart:	n/a	n/a
29	CTCF	chr3:51740800-51740950	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr3:51740820-51740970	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr3:51740840-51740990	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr3:51740880-51741030	HVMF	connective:	n/a	n/a
33	CTCF	chr3:51740820-51740970	HEK293	kidney:	n/a	n/a
34	CTCF	chr3:51740840-51740990	AG04449	skin:	n/a	n/a
35	CTCF	chr3:51740860-51741010	BJ	skin:	n/a	n/a
36	E2F6	chr3:51740935-51741594	H1-hESC	embryonic stem cell:	n/a	n/a
37	E2F6	chr3:51740850-51741682	H1-hESC	embryonic stem cell:	n/a	n/a
38	EGR1	chr3:51740823-51740988	K562	blood:	n/a	n/a
39	EGR1	chr3:51740815-51741002	K562	blood:	n/a	n/a
40	ELF1	chr3:51741295-51741706	GM12878	blood:	n/a	n/a
41	EP300	chr3:51740767-51740996	H1-hESC	embryonic stem cell:	n/a	n/a
42	EP300	chr3:51740650-51741266	ECC-1	luminal epithelium:	n/a	n/a
43	ETS1	chr3:51740787-51740988	K562	blood:	n/a	n/a
44	FOXP2	chr3:51740810-51741008	PFSK-1	brain:	n/a	n/a
45	GABPA	chr3:51741042-51741448	H1-hESC	embryonic stem cell:	n/a	chr3:51741075-51741084
46	GABPA	chr3:51740784-51740990	H1-hESC	embryonic stem cell:	n/a	n/a
47	GTF2F1	chr3:51740818-51740951	H1-hESC	embryonic stem cell:	n/a	n/a
48	GTF2F1	chr3:51741223-51741301	H1-hESC	embryonic stem cell:	n/a	n/a
49	HA-E2F1	chr3:51741112-51741530	MCF-7	breast:	n/a	n/a
50	HCFC1	chr3:51740787-51741047	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51740896-51740946	PFSK-1	brain:	n/a
2	chr3:51740896-51740946	PFSK-1	brain:	n/a
3	chr3:51741135-51741185	Hepatocyte	liver:	n/a
4	chr3:51741135-51741185	NHBE	bronchial:	n/a
5	chr3:51740896-51740946	AG04450	lung:	fetal
6	chr3:51740850-51740900	MCF10A-Er-Src	breast:	n/a
7	chr3:51740875-51740925	BJ	skin:	n/a
8	chr3:51741135-51741185	HNPCEpiC	eye:	n/a
9	chr3:51741280-51741330	SK-N-SH_RA	brain:	n/a
10	chr3:51741473-51741523	GM12892	blood:	n/a
11	chr3:51740896-51740946	HCPEpiC	choroid plexus:	n/a
12	chr3:51740875-51740925	AG04450	lung:	fetal
13	chr3:51740741-51740791	HIPEpiC	eye:	n/a
14	chr3:51740896-51740946	NT2-D1	testis:	n/a
15	chr3:51741135-51741185	HUVEC	blood vessel:	n/a
16	chr3:51741473-51741523	PANC-1	pancreas:	n/a
17	chr3:51740875-51740925	BE2_C	brain:	n/a
18	chr3:51740875-51740925	Hela-S3	cervix:	n/a
19	chr3:51740741-51740791	GM06990	blood:	n/a
20	chr3:51741280-51741330	HUVEC	blood vessel:	n/a
21	chr3:51740896-51740946	HPAEpiC	pulmonary alveolar:	n/a
22	chr3:51740896-51740946	HCT-116	colon:	n/a
23	chr3:51740896-51740946	HepG2	liver:	n/a
24	chr3:51740850-51740900	NT2-D1	testis:	n/a
25	chr3:51741280-51741330	HEEpiC	esophagus:	n/a
26	chr3:51740741-51740791	HRCEpiC	kidney:	n/a
27	chr3:51741280-51741330	NH-A	brain:	n/a
28	chr3:51741473-51741523	U87	brain:	n/a
29	chr3:51741135-51741185	Caco-2	colon:	n/a
30	chr3:51740875-51740925	SKMC	muscle:	n/a
31	chr3:51740850-51740900	Caco-2	colon:	n/a
32	chr3:51740875-51740925	HNPCEpiC	eye:	n/a
33	chr3:51740850-51740900	HCT-116	colon:	n/a
34	chr3:51740741-51740791	HEEpiC	esophagus:	n/a
35	chr3:51740850-51740900	HepG2	liver:	n/a
36	chr3:51741280-51741330	Hela-S3	cervix:	n/a
37	chr3:51741135-51741185	HCT-116	colon:	n/a
38	chr3:51740741-51740791	A549	lung:	n/a
39	chr3:51740850-51740900	GM12892	blood:	n/a
40	chr3:51741473-51741523	BE2_C	brain:	n/a
41	chr3:51740850-51740900	BJ	skin:	n/a
42	chr3:51740875-51740925	GM06990	blood:	n/a
43	chr3:51741280-51741330	HEK293	kidney:	embryo
44	chr3:51740850-51740900	PANC-1	pancreas:	n/a
45	chr3:51741135-51741185	HIPEpiC	eye:	n/a
46	chr3:51740850-51740900	AG09309	skin:	n/a
47	chr3:51741135-51741185	ProgFib	skin:	n/a
48	chr3:51740875-51740925	SK-N-SH	brain:	n/a
49	chr3:51741135-51741185	AoSMC	blood vessel:	n/a
50	chr3:51741280-51741330	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:51739711..51741988-chr3:51976226..51978640,2	K562	blood:

No data

Variant related genes	Relation type
GRM2	TF binding region
GRM2	CpG island
ENSG00000041880	chromatin interactions

Extended variants
information (count: 51 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:51 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145899880	chr3:51740275-51740276	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs111925214	chr3:51740289-51740290	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560089890	chr3:51740335-51740336	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs138183384	chr3:51740339-51740340	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142785768	chr3:51740420-51740421	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs375824692	chr3:51740428-51740429	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs558205942	chr3:51740436-51740437	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185782416	chr3:51740440-51740441	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs532745454	chr3:51740446-51740447	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs551364491	chr3:51740451-51740452	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551947529	chr3:51740515-51740516	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs571021428	chr3:51740525-51740526	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375923849	chr3:51740528-51740529	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs145013769	chr3:51740538-51740539	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs546766046	chr3:51740587-51740588	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs568347085	chr3:51740640-51740641	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs535541481	chr3:51740677-51740678	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs557082868	chr3:51740739-51740740	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs60497133	chr3:51740791-51740792	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs539412875	chr3:51740850-51740851	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs558149496	chr3:51740853-51740854	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs114774669	chr3:51740930-51740931	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs540550863	chr3:51740932-51740933	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs555585892	chr3:51741007-51741008	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368654699	chr3:51741063-51741064	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs577811602	chr3:51741111-51741112	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561596345	chr3:51741136-51741137	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs149387441	chr3:51741138-51741139	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544422490	chr3:51741139-51741140	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200682913	chr3:51741196-51741197	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs562527677	chr3:51741211-51741212	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs533062004	chr3:51741216-51741217	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs544649692	chr3:51741283-51741284	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs531288431	chr3:51741284-51741285	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs528763644	chr3:51741445-51741446	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs546927374	chr3:51741452-51741453	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs191645778	chr3:51741467-51741468	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529402763	chr3:51741470-51741471	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs540382508	chr3:51741502-51741503	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148456775	chr3:51741512-51741513	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569221179	chr3:51741517-51741518	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs539946071	chr3:51741520-51741521	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs34507460	chr3:51741581-51741582	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551464949	chr3:51741703-51741704	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs553957592	chr3:51741747-51741748	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs534071420	chr3:51741769-51741770	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs555653241	chr3:51741791-51741792	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs369460688	chr3:51741807-51741808	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs182272540	chr3:51741823-51741824	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs143692524	chr3:51741824-51741825	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	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
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
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51706400-51741000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:51707800-51740400	Strong transcription	Fetal Intestine Small	intestine
3	chr3:51716400-51741200	Weak transcription	Fetal Kidney	kidney
4	chr3:51719600-51741200	Weak transcription	NHDF-Ad	bronchial
5	chr3:51721000-51741000	Weak transcription	HUVEC	blood vessel
6	chr3:51721400-51740400	Strong transcription	Dnd41	blood
7	chr3:51721400-51740600	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr3:51721400-51740800	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr3:51721600-51740400	Strong transcription	Fetal Stomach	stomach
10	chr3:51721600-51740800	Weak transcription	HSMM	muscle
11	chr3:51722600-51741200	Weak transcription	Stomach Mucosa	stomach
12	chr3:51724000-51740400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr3:51724400-51741200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr3:51725400-51740800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr3:51729200-51740400	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr3:51730400-51740400	Strong transcription	Pancreas	Pancrea
17	chr3:51733000-51741400	Weak transcription	Fetal Heart	heart
18	chr3:51734000-51741200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr3:51734000-51741200	Weak transcription	NH-A	brain
20	chr3:51734400-51740400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr3:51734600-51740600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr3:51734600-51741400	Weak transcription	Fetal Lung	lung
23	chr3:51734600-51741600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr3:51735000-51741200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr3:51735200-51741200	Weak transcription	HepG2	liver
26	chr3:51735200-51741200	Weak transcription	Osteobl	bone
27	chr3:51736400-51741400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr3:51737000-51741200	Weak transcription	Colon Smooth Muscle	Colon
29	chr3:51737400-51741200	Weak transcription	HMEC	breast
30	chr3:51738200-51740400	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr3:51738200-51741200	Weak transcription	Fetal Thymus	thymus
32	chr3:51738400-51740400	Weak transcription	Brain Germinal Matrix	brain
33	chr3:51738400-51740400	Genic enhancers	Spleen	Spleen
34	chr3:51738400-51741200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:51738400-51743400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr3:51738800-51740400	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr3:51738800-51741000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:51738800-51741000	Weak transcription	NHEK	skin
39	chr3:51738800-51741200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr3:51738800-51741200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr3:51738800-51741200	Weak transcription	Fetal Intestine Large	intestine
42	chr3:51738800-51741400	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr3:51739000-51740400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:51739000-51740400	Weak transcription	Fetal Muscle Trunk	muscle
45	chr3:51739000-51741000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr3:51739000-51741000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr3:51739200-51740400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr3:51739200-51741000	Weak transcription	Fetal Muscle Leg	muscle
49	chr3:51739200-51741200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:51739400-51741000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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