Variant report

Variant	esv3358545
Chromosome Location	chr14:37049026-37051574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:100)
CpG islands
(count:488)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:100 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:37050966-37050999	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:37050310-37050435	H1-hESC	embryonic stem cell:	n/a	n/a
3	CREB1	chr14:37049964-37050491	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTBP2	chr14:37048727-37050904	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr14:37050169-37050234	MCF-7	breast:	n/a	n/a
6	CTCF	chr14:37050100-37050250	AG09319	gingival:	n/a	n/a
7	CTCF	chr14:37051520-37051670	HEK293	kidney:	n/a	n/a
8	CTCF	chr14:37050161-37050223	LNCaP	prostate:	n/a	n/a
9	CTCF	chr14:37050400-37050550	Caco-2	colon:	n/a	n/a
10	CTCF	chr14:37050337-37050430	MCF-7	breast:	n/a	n/a
11	CTCF	chr14:37050123-37050238	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr14:37050060-37050210	HAc	cerebellar:	n/a	n/a
13	CTCF	chr14:37050060-37050210	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr14:37050100-37050250	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr14:37050661-37050731	MCF-7	breast:	n/a	n/a
16	CTCF	chr14:37050480-37050630	NHEK	skin:	n/a	n/a
17	CTCF	chr14:37051400-37051550	SAEC	small airway:	n/a	n/a
18	CTCF	chr14:37050265-37050422	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:37050447-37050517	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:37050200-37050350	GM12871	blood:	n/a	n/a
21	CTCF	chr14:37050340-37050374	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:37050380-37050530	SAEC	small airway:	n/a	n/a
23	E2F4	chr14:37050367-37050742	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr14:37050227-37050814	A549	lung:	n/a	n/a
25	E2F6	chr14:37050108-37051092	A549	lung:	n/a	n/a
26	EGR1	chr14:37049918-37050649	H1-hESC	embryonic stem cell:	n/a	n/a
27	EGR1	chr14:37050138-37050920	MCF-7	breast:	n/a	n/a
28	EGR1	chr14:37050271-37050717	ECC-1	luminal epithelium:	n/a	n/a
29	EGR1	chr14:37050203-37050791	MCF-7	breast:	n/a	n/a
30	EGR1	chr14:37051330-37052012	HCT-116	colon:	n/a	chr14:37051605-37051618 chr14:37051610-37051620 chr14:37051611-37051624
31	EGR1	chr14:37050347-37050560	K562	blood:	n/a	n/a
32	EGR1	chr14:37050185-37050758	ECC-1	luminal epithelium:	n/a	n/a
33	ELF1	chr14:37050097-37051127	MCF-7	breast:	n/a	n/a
34	GABPA	chr14:37049998-37050711	H1-hESC	embryonic stem cell:	n/a	n/a
35	GABPA	chr14:37050196-37050919	MCF-7	breast:	n/a	n/a
36	HDAC2	chr14:37049924-37050977	MCF-7	breast:	n/a	n/a
37	JUN	chr14:37050072-37050197	H1-hESC	embryonic stem cell:	n/a	n/a
38	JUND	chr14:37049357-37049716	H1-hESC	embryonic stem cell:	n/a	chr14:37049483-37049493 chr14:37049483-37049493
39	JUND	chr14:37050689-37050949	HepG2	liver:	n/a	n/a
40	JUND	chr14:37050834-37050865	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAX	chr14:37051407-37051767	H1-hESC	embryonic stem cell:	n/a	chr14:37051687-37051696 chr14:37051611-37051621
42	MAX	chr14:37050150-37050941	A549	lung:	n/a	n/a
43	MAX	chr14:37050077-37050829	ECC-1	luminal epithelium:	n/a	n/a
44	MAX	chr14:37051158-37051914	A549	lung:	n/a	chr14:37051387-37051396 chr14:37051687-37051696 chr14:37051611-37051621
45	MAX	chr14:37050014-37050632	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr14:37050295-37050642	A549	lung:	n/a	n/a
47	MAX	chr14:37049998-37051153	A549	lung:	n/a	chr14:37051121-37051131
48	MAX	chr14:37051125-37051878	MCF-7	breast:	n/a	chr14:37051387-37051396 chr14:37051687-37051696 chr14:37051611-37051621
49	MAX	chr14:37051333-37051831	ECC-1	luminal epithelium:	n/a	chr14:37051387-37051396 chr14:37051687-37051696 chr14:37051611-37051621
50	MAX	chr14:37050079-37050968	MCF-7	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37049299-37049349	HepG2	liver:	n/a
2	chr14:37050403-37050453	HL-60	blood:	n/a
3	chr14:37050403-37050453	HRCEpiC	kidney:	n/a
4	chr14:37049299-37049349	AG10803	skin:	n/a
5	chr14:37050691-37050741	RPTEC	kidney:	n/a
6	chr14:37050403-37050453	HEK293	kidney:	embryo
7	chr14:37050455-37050505	HRE	kidney:	n/a
8	chr14:37050455-37050505	HCF	heart:	n/a
9	chr14:37049893-37049943	AG04449	skin:	fetal
10	chr14:37050403-37050453	NHDF-neo	bronchial:	n/a
11	chr14:37050403-37050453	AoSMC	blood vessel:	n/a
12	chr14:37049565-37049615	GM19239	blood:	n/a
13	chr14:37051417-37051467	HRCEpiC	kidney:	n/a
14	chr14:37049893-37049943	HRCEpiC	kidney:	n/a
15	chr14:37049893-37049943	ECC-1	luminal epithelium:	n/a
16	chr14:37050403-37050453	U87	brain:	n/a
17	chr14:37049565-37049615	SK-N-MC	brain:	n/a
18	chr14:37049893-37049943	HIPEpiC	eye:	n/a
19	chr14:37050455-37050505	PrEC	prostate:	n/a
20	chr14:37049091-37049141	HCPEpiC	choroid plexus:	n/a
21	chr14:37049565-37049615	Hepatocyte	liver:	n/a
22	chr14:37049091-37049141	HRE	kidney:	n/a
23	chr14:37049565-37049615	GM12878	blood:	n/a
24	chr14:37049091-37049141	U87	brain:	n/a
25	chr14:37049565-37049615	HRCEpiC	kidney:	n/a
26	chr14:37051417-37051467	NT2-D1	testis:	n/a
27	chr14:37049091-37049141	GM19239	blood:	n/a
28	chr14:37049893-37049943	HepG2	liver:	n/a
29	chr14:37049091-37049141	GM12878	blood:	n/a
30	chr14:37051417-37051467	MCF10A-Er-Src	breast:	n/a
31	chr14:37051417-37051467	IMR90	lung:	fetal
32	chr14:37049893-37049943	AG09319	gingival:	n/a
33	chr14:37050691-37050741	GM12892	blood:	n/a
34	chr14:37049299-37049349	HCF	heart:	n/a
35	chr14:37051417-37051467	U87	brain:	n/a
36	chr14:37049091-37049141	HCM	heart:	n/a
37	chr14:37050455-37050505	Hela-S3	cervix:	n/a
38	chr14:37049893-37049943	AG04450	lung:	fetal
39	chr14:37050455-37050505	Jurkat	blood:	n/a
40	chr14:37049299-37049349	NT2-D1	testis:	n/a
41	chr14:37049299-37049349	AG04449	skin:	fetal
42	chr14:37049299-37049349	AG04450	lung:	fetal
43	chr14:37050691-37050741	AG10803	skin:	n/a
44	chr14:37049091-37049141	HRPEpiC	eye:	n/a
45	chr14:37049299-37049349	HMEC	breast:	n/a
46	chr14:37049565-37049615	BE2_C	brain:	n/a
47	chr14:37049893-37049943	NB4	blood:	n/a
48	chr14:37049091-37049141	Caco-2	colon:	n/a
49	chr14:37049299-37049349	HCT-116	colon:	n/a
50	chr14:37049091-37049141	ECC-1	luminal epithelium:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:37043777..37046012-chr14:37049120..37051344,2	MCF-7	breast:
2	chr14:37047412..37050390-chr14:37058985..37061085,2	MCF-7	breast:
3	chr14:37049506..37051705-chr14:37066092..37068033,2	MCF-7	breast:
4	chr14:37043733..37045700-chr14:37047521..37049850,2	K562	blood:
5	chr14:37043733..37046735-chr14:37047521..37050393,3	K562	blood:

No data

Variant related genes	Relation type
RPL29P3	TF binding region
RPL29P3	CpG island

Extended variants
information (count: 104 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:104 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552171144	chr14:37049035-37049036	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs529164242	chr14:37049048-37049049	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs555442383	chr14:37049058-37049059	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs138271395	chr14:37049065-37049066	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs189449354	chr14:37049099-37049100	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs61994881	chr14:37049126-37049127	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs572918000	chr14:37049129-37049130	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs540198260	chr14:37049138-37049139	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs549041335	chr14:37049227-37049228	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs537144581	chr14:37049246-37049247	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs368636368	chr14:37049257-37049258	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs115560066	chr14:37049321-37049322	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs371919968	chr14:37049406-37049407	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs374895693	chr14:37049507-37049508	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565636310	chr14:37049588-37049589	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs177325	chr14:37049596-37049597	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539448900	chr14:37049603-37049604	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs74949744	chr14:37049606-37049607	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs573522402	chr14:37049620-37049621	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs535613850	chr14:37049661-37049662	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs555545175	chr14:37049688-37049689	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs575307673	chr14:37049705-37049706	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs112735619	chr14:37049706-37049707	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs544313777	chr14:37049809-37049810	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564272951	chr14:37049838-37049839	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs577936008	chr14:37049864-37049865	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs116790025	chr14:37049888-37049889	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs369728623	chr14:37049903-37049904	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs559375756	chr14:37049919-37049920	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs528392559	chr14:37049937-37049938	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs548356463	chr14:37049950-37049951	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs180686469	chr14:37049951-37049952	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs530761587	chr14:37049977-37049978	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs561772352	chr14:37049984-37049985	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs12888574	chr14:37049991-37049992	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs550675195	chr14:37050010-37050011	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs528098264	chr14:37050017-37050018	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs112240157	chr14:37050022-37050023	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs552023200	chr14:37050030-37050031	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs369637676	chr14:37050060-37050061	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs371825303	chr14:37050067-37050068	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs374997840	chr14:37050084-37050085	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369093110	chr14:37050110-37050111	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs200754327	chr14:37050154-37050155	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs372555629	chr14:37050200-37050201	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs567008454	chr14:37050236-37050237	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs564201727	chr14:37050265-37050266	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs535768677	chr14:37050268-37050269	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs555505864	chr14:37050295-37050296	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs200062685	chr14:37050339-37050340	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD

Chromatin state (count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37048000-37054800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr14:37048400-37050000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr14:37048400-37050200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:37048600-37049200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:37048800-37049200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
6	chr14:37048800-37049600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
7	chr14:37048800-37050200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:37048800-37050600	ZNF genes & repeats	Spleen	Spleen
9	chr14:37048800-37051800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr14:37049000-37049200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
11	chr14:37049000-37049200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:37049000-37049400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
13	chr14:37049000-37049400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr14:37049000-37049400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr14:37049000-37049400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
16	chr14:37049000-37049400	Active TSS	Brain Substantia Nigra	brain
17	chr14:37049000-37052400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
18	chr14:37049200-37049400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
19	chr14:37049200-37049400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
20	chr14:37049200-37049400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr14:37049200-37049400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
22	chr14:37049200-37049400	Bivalent Enhancer	Brain Hippocampus Middle	brain
23	chr14:37049200-37049800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr14:37049200-37050000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
25	chr14:37049200-37050400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr14:37049200-37051800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
27	chr14:37049400-37049600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
28	chr14:37049400-37049600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
29	chr14:37049400-37049600	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr14:37049400-37049600	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
31	chr14:37049400-37049600	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
32	chr14:37049400-37049800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
33	chr14:37049400-37049800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
34	chr14:37049400-37049800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
35	chr14:37049400-37050000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
36	chr14:37049400-37050200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr14:37049400-37050400	Bivalent Enhancer	Left Ventricle	heart
38	chr14:37049400-37050800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr14:37049400-37051000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
40	chr14:37049400-37051000	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
41	chr14:37049600-37049800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
42	chr14:37049600-37049800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr14:37049600-37049800	Bivalent Enhancer	Brain Germinal Matrix	brain
44	chr14:37049600-37050000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr14:37049600-37050000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
46	chr14:37049600-37050000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr14:37049600-37050000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:37049600-37050000	Bivalent Enhancer	Esophagus	oesophagus
49	chr14:37049600-37050000	Enhancers	Pancreas	Pancrea
50	chr14:37049600-37050200	Bivalent Enhancer	Colonic Mucosa	Colon

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