Variant report

Variant	esv32575
Chromosome Location	chr14:37047629-37052658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:978)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:37050310-37050435	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:37050966-37050999	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	CTBP2	chr14:37051980-37054092	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr14:37050200-37050350	GM12871	blood:	n/a	n/a
7	CTCF	chr14:37050400-37050550	Caco-2	colon:	n/a	n/a
8	CTCF	chr14:37050337-37050430	MCF-7	breast:	n/a	n/a
9	CTCF	chr14:37051520-37051670	HEK293	kidney:	n/a	n/a
10	CTCF	chr14:37050123-37050238	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr14:37050060-37050210	HAc	cerebellar:	n/a	n/a
12	CTCF	chr14:37050661-37050731	MCF-7	breast:	n/a	n/a
13	CTCF	chr14:37050100-37050250	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr14:37050060-37050210	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr14:37048591-37048618	Lung_OC	lung:	n/a	n/a
16	CTCF	chr14:37050161-37050223	LNCaP	prostate:	n/a	n/a
17	CTCF	chr14:37050380-37050530	SAEC	small airway:	n/a	n/a
18	CTCF	chr14:37050447-37050517	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:37050340-37050374	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:37050480-37050630	NHEK	skin:	n/a	n/a
21	CTCF	chr14:37050100-37050250	AG09319	gingival:	n/a	n/a
22	CTCF	chr14:37050265-37050422	MCF-7	breast:	n/a	n/a
23	CTCF	chr14:37050169-37050234	MCF-7	breast:	n/a	n/a
24	CTCF	chr14:37051400-37051550	SAEC	small airway:	n/a	n/a
25	E2F4	chr14:37050367-37050742	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F6	chr14:37050108-37051092	A549	lung:	n/a	n/a
27	E2F6	chr14:37050227-37050814	A549	lung:	n/a	n/a
28	EGR1	chr14:37050185-37050758	ECC-1	luminal epithelium:	n/a	n/a
29	EGR1	chr14:37050271-37050717	ECC-1	luminal epithelium:	n/a	n/a
30	EGR1	chr14:37050138-37050920	MCF-7	breast:	n/a	n/a
31	EGR1	chr14:37050347-37050560	K562	blood:	n/a	n/a
32	EGR1	chr14:37051330-37052012	HCT-116	colon:	n/a	chr14:37051605-37051618 chr14:37051610-37051620 chr14:37051611-37051624
33	EGR1	chr14:37050203-37050791	MCF-7	breast:	n/a	n/a
34	EGR1	chr14:37049918-37050649	H1-hESC	embryonic stem cell:	n/a	n/a
35	ELF1	chr14:37050097-37051127	MCF-7	breast:	n/a	n/a
36	GABPA	chr14:37050196-37050919	MCF-7	breast:	n/a	n/a
37	GABPA	chr14:37049998-37050711	H1-hESC	embryonic stem cell:	n/a	n/a
38	HDAC2	chr14:37049924-37050977	MCF-7	breast:	n/a	n/a
39	JUN	chr14:37050072-37050197	H1-hESC	embryonic stem cell:	n/a	n/a
40	JUND	chr14:37050689-37050949	HepG2	liver:	n/a	n/a
41	JUND	chr14:37049357-37049716	H1-hESC	embryonic stem cell:	n/a	chr14:37049483-37049493 chr14:37049483-37049493
42	JUND	chr14:37050834-37050865	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAX	chr14:37050071-37050791	ECC-1	luminal epithelium:	n/a	n/a
44	MAX	chr14:37050150-37050941	A549	lung:	n/a	n/a
45	MAX	chr14:37051125-37051878	MCF-7	breast:	n/a	chr14:37051387-37051396 chr14:37051687-37051696 chr14:37051611-37051621
46	MAX	chr14:37049998-37051153	A549	lung:	n/a	chr14:37051121-37051131
47	MAX	chr14:37050295-37050642	A549	lung:	n/a	n/a
48	MAX	chr14:37051333-37051831	ECC-1	luminal epithelium:	n/a	chr14:37051387-37051396 chr14:37051687-37051696 chr14:37051611-37051621
49	MAX	chr14:37050079-37050968	MCF-7	breast:	n/a	n/a
50	MAX	chr14:37050077-37050829	ECC-1	luminal epithelium:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37052470-37052520	SK-N-MC	brain:	n/a
2	chr14:37049893-37049943	MCF-7	breast:	n/a
3	chr14:37052470-37052520	SK-N-MC	brain:	n/a
4	chr14:37049893-37049943	MCF-7	breast:	n/a
5	chr14:37049893-37049943	AG09319	gingival:	n/a
6	chr14:37049091-37049141	SKMC	muscle:	n/a
7	chr14:37052470-37052520	HRPEpiC	eye:	n/a
8	chr14:37051902-37051952	K562	blood:	n/a
9	chr14:37051873-37051923	SK-N-SH_RA	brain:	n/a
10	chr14:37051703-37051753	H1-hESC	embryonic stem cell:	embryo
11	chr14:37051693-37051743	LNCaP	prostate:	n/a
12	chr14:37051863-37051913	AoSMC	blood vessel:	n/a
13	chr14:37051703-37051753	ECC-1	luminal epithelium:	n/a
14	chr14:37050691-37050741	HAEpiC	amniotic membrane:	n/a
15	chr14:37051902-37051952	HIPEpiC	eye:	n/a
16	chr14:37050455-37050505	SK-N-SH	brain:	n/a
17	chr14:37051873-37051923	NB4	blood:	n/a
18	chr14:37050691-37050741	HCF	heart:	n/a
19	chr14:37051417-37051467	U87	brain:	n/a
20	chr14:37050403-37050453	AG04450	lung:	fetal
21	chr14:37051703-37051753	HCPEpiC	choroid plexus:	n/a
22	chr14:37051693-37051743	NHDF-neo	bronchial:	n/a
23	chr14:37051902-37051952	PANC-1	pancreas:	n/a
24	chr14:37050691-37050741	K562	blood:	n/a
25	chr14:37050455-37050505	HCM	heart:	n/a
26	chr14:37051693-37051743	HCT-116	colon:	n/a
27	chr14:37051949-37051999	AG04450	lung:	fetal
28	chr14:37050455-37050505	Jurkat	blood:	n/a
29	chr14:37052470-37052520	HUVEC	blood vessel:	n/a
30	chr14:37051949-37051999	NT2-D1	testis:	n/a
31	chr14:37049299-37049349	AoSMC	blood vessel:	n/a
32	chr14:37049565-37049615	HCPEpiC	choroid plexus:	n/a
33	chr14:37050455-37050505	HepG2	liver:	n/a
34	chr14:37051949-37051999	LNCaP	prostate:	n/a
35	chr14:37051703-37051753	HepG2	liver:	n/a
36	chr14:37050455-37050505	MCF10A-Er-Src	breast:	n/a
37	chr14:37050691-37050741	BE2_C	brain:	n/a
38	chr14:37051693-37051743	SK-N-SH_RA	brain:	n/a
39	chr14:37051703-37051753	HL-60	blood:	n/a
40	chr14:37049091-37049141	BJ	skin:	n/a
41	chr14:37051863-37051913	CMK	blood:	n/a
42	chr14:37051949-37051999	AG09319	gingival:	n/a
43	chr14:37050403-37050453	PFSK-1	brain:	n/a
44	chr14:37051902-37051952	HRPEpiC	eye:	n/a
45	chr14:37051777-37051827	HRPEpiC	eye:	n/a
46	chr14:37050403-37050453	Jurkat	blood:	n/a
47	chr14:37051949-37051999	Jurkat	blood:	n/a
48	chr14:37051693-37051743	H1-hESC	embryonic stem cell:	embryo
49	chr14:37049299-37049349	MCF10A-Er-Src	breast:	n/a
50	chr14:37050403-37050453	HRE	kidney:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:37051690..37053277-chr14:37640298..37642030,2	K562	blood:
2	chr14:37043777..37046012-chr14:37049120..37051344,2	MCF-7	breast:
3	chr14:37043733..37045700-chr14:37047521..37049850,2	K562	blood:
4	chr14:37049506..37051705-chr14:37066092..37068033,2	MCF-7	breast:
5	chr14:37047412..37050390-chr14:37058985..37061085,2	MCF-7	breast:
6	chr14:37043733..37046735-chr14:37047521..37050393,3	K562	blood:

No data

Variant related genes	Relation type
NKX2-8	TF binding region
RPL29P3	TF binding region
NKX2-8	CpG island
RPL29P3	CpG island
ENSG00000258708	chromatin interactions
ENSG00000183032	chromatin interactions

Extended variants
information (count: 179 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:179 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568169087	chr14:37047809-37047810	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs177326	chr14:37047819-37047820	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs34568843	chr14:37047821-37047822	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs8008136	chr14:37047902-37047903	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs530811648	chr14:37047920-37047921	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs550603825	chr14:37047932-37047933	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs35640449	chr14:37047957-37047958	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs563383091	chr14:37047972-37047973	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs532308774	chr14:37047986-37047987	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs77123291	chr14:37047993-37047994	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs377301424	chr14:37048017-37048018	Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs7149537	chr14:37048062-37048063	Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs556845118	chr14:37048071-37048072	Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs8012731	chr14:37048168-37048169	Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs8013674	chr14:37048218-37048219	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs8012535	chr14:37048322-37048323	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189700766	chr14:37048362-37048363	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554682298	chr14:37048392-37048393	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575381493	chr14:37048436-37048437	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs568206233	chr14:37048458-37048459	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs368373462	chr14:37048476-37048477	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs537032907	chr14:37048583-37048584	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs140452864	chr14:37048640-37048641	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs577563503	chr14:37048667-37048668	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546197701	chr14:37048700-37048701	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs192883421	chr14:37048702-37048703	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs371798478	chr14:37048710-37048711	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs539380446	chr14:37048724-37048725	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs573337380	chr14:37048725-37048726	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs542457470	chr14:37048732-37048733	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs561838006	chr14:37048792-37048793	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs530921272	chr14:37048813-37048814	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs35871433	chr14:37048871-37048872	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs184513811	chr14:37048904-37048905	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs147047540	chr14:37048918-37048919	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs376728485	chr14:37048977-37048978	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs532402021	chr14:37048981-37048982	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558031099	chr14:37049022-37049023	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37047800-37048000	Bivalent Enhancer	Brain Hippocampus Middle	brain
2	chr14:37047800-37048200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr14:37048000-37054800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr14:37048200-37048400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:37048200-37048800	Enhancers	Brain Substantia Nigra	brain
6	chr14:37048200-37048800	Weak transcription	Spleen	Spleen
7	chr14:37048400-37048600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr14:37048400-37048800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
9	chr14:37048400-37048800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
10	chr14:37048400-37048800	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
11	chr14:37048400-37050000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr14:37048400-37050200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:37048600-37049200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:37048800-37049000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
15	chr14:37048800-37049000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
16	chr14:37048800-37049000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:37048800-37049000	Bivalent Enhancer	Brain Anterior Caudate	brain
18	chr14:37048800-37049000	Flanking Active TSS	Brain Substantia Nigra	brain
19	chr14:37048800-37049000	Bivalent Enhancer	Fetal Brain Female	brain
20	chr14:37048800-37049200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
21	chr14:37048800-37049600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
22	chr14:37048800-37050200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr14:37048800-37050600	ZNF genes & repeats	Spleen	Spleen
24	chr14:37048800-37051800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
25	chr14:37049000-37049200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
26	chr14:37049000-37049200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:37049000-37049400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
28	chr14:37049000-37049400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
29	chr14:37049000-37049400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr14:37049000-37049400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
31	chr14:37049000-37049400	Active TSS	Brain Substantia Nigra	brain
32	chr14:37049000-37052400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
33	chr14:37049200-37049400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
34	chr14:37049200-37049400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
35	chr14:37049200-37049400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:37049200-37049400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
37	chr14:37049200-37049400	Bivalent Enhancer	Brain Hippocampus Middle	brain
38	chr14:37049200-37049800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr14:37049200-37050000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
40	chr14:37049200-37050400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr14:37049200-37051800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
42	chr14:37049400-37049600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
43	chr14:37049400-37049600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
44	chr14:37049400-37049600	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr14:37049400-37049600	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
46	chr14:37049400-37049600	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
47	chr14:37049400-37049800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
48	chr14:37049400-37049800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
49	chr14:37049400-37049800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
50	chr14:37049400-37050000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle

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