Variant report

Variant	esv3425540
Chromosome Location	chr14:72397724-72400572
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	BATF	chr14:72400109-72400450	GM12878	blood:	n/a	n/a
2	BATF	chr14:72400148-72400401	GM12878	blood:	n/a	n/a
3	BCL3	chr14:72398918-72399258	GM12878	blood:	n/a	chr14:72398995-72399008 chr14:72398962-72398975 chr14:72398955-72398968 chr14:72399111-72399124 chr14:72398960-72398969
4	BCLAF1	chr14:72398928-72399421	GM12878	blood:	n/a	chr14:72398995-72399008 chr14:72398962-72398975 chr14:72398955-72398968 chr14:72399111-72399124 chr14:72398960-72398969
5	BCLAF1	chr14:72399008-72399294	GM12878	blood:	n/a	chr14:72399111-72399124
6	BHLHE40	chr14:72398884-72399276	GM12878	blood:	n/a	chr14:72399122-72399138
7	BHLHE40	chr14:72399725-72399936	GM12878	blood:	n/a	n/a
8	BRCA1	chr14:72398988-72399284	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr14:72398564-72399380	HCT-116	colon:	n/a	n/a
10	CEBPB	chr14:72398955-72399284	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr14:72399095-72399420	GM12878	blood:	n/a	chr14:72399288-72399298
12	CHD1	chr14:72399089-72399344	H1-hESC	embryonic stem cell:	n/a	chr14:72399288-72399298
13	CHD2	chr14:72398573-72399342	H1-hESC	embryonic stem cell:	n/a	chr14:72399288-72399298
14	CHD2	chr14:72399685-72399801	GM12878	blood:	n/a	n/a
15	CHD2	chr14:72399063-72399400	GM12878	blood:	n/a	chr14:72399288-72399298
16	CTBP2	chr14:72398707-72399608	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr14:72399020-72399170	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr14:72399805-72400359	GM12878	blood:	n/a	n/a
19	CTCF	chr14:72400180-72400330	GM12873	blood:	n/a	n/a
20	CTCF	chr14:72399060-72399210	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr14:72399060-72399210	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr14:72398603-72399332	MCF-7	breast:	n/a	chr14:72399007-72399020
23	CTCF	chr14:72398981-72399188	Spleen_OC	spleen:	n/a	chr14:72399007-72399020
24	CTCF	chr14:72399040-72399190	HEK293	kidney:	n/a	n/a
25	CTCF	chr14:72400180-72400330	GM12875	blood:	n/a	n/a
26	CTCF	chr14:72398700-72398850	GM12865	blood:	n/a	n/a
27	CTCF	chr14:72400167-72400309	GM12892	blood:	n/a	n/a
28	CTCF	chr14:72399025-72399187	HepG2	liver:	n/a	n/a
29	CTCF	chr14:72399040-72399190	GM12878	blood:	n/a	n/a
30	CTCF	chr14:72399001-72399007	Lung_OC	lung:	n/a	n/a
31	CTCF	chr14:72399060-72399210	HEK293	kidney:	n/a	n/a
32	CTCF	chr14:72398637-72398751	GM19239	blood:	n/a	n/a
33	CTCF	chr14:72398700-72398850	HEK293	kidney:	n/a	n/a
34	CTCF	chr14:72398922-72399257	A549	lung:	n/a	chr14:72399007-72399020
35	CTCF	chr14:72398620-72399308	T-47D	breast:	n/a	chr14:72399007-72399020
36	CTCF	chr14:72400200-72400350	GM12878	blood:	n/a	n/a
37	CTCF	chr14:72399020-72399170	GM12875	blood:	n/a	n/a
38	CTCF	chr14:72399040-72399190	GM12871	blood:	n/a	n/a
39	CTCF	chr14:72398579-72398830	Medullo	brain:	n/a	n/a
40	CTCF	chr14:72398600-72398750	GM12874	blood:	n/a	n/a
41	CTCF	chr14:72399040-72399190	GM12872	blood:	n/a	n/a
42	CTCF	chr14:72398988-72399216	GM20000	blood:	n/a	chr14:72399007-72399020
43	CTCF	chr14:72400220-72400370	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:72398600-72398750	GM06990	blood:	n/a	n/a
45	CTCF	chr14:72398803-72399278	MCF-7	breast:	n/a	chr14:72399007-72399020
46	CTCF	chr14:72399020-72399170	GM12872	blood:	n/a	n/a
47	CTCF	chr14:72398776-72399314	H1-hESC	embryonic stem cell:	n/a	chr14:72399007-72399020
48	CTCF	chr14:72398903-72399239	NHEK	skin:	n/a	chr14:72399007-72399020
49	CTCF	chr14:72398874-72399258	H1-hESC	embryonic stem cell:	n/a	chr14:72399007-72399020
50	CTCF	chr14:72399000-72399150	HCT-116	colon:	n/a	chr14:72399007-72399020

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:72399809-72399859	Caco-2	colon:	n/a
2	chr14:72398920-72398970	NHDF-neo	bronchial:	n/a
3	chr14:72398920-72398970	PANC-1	pancreas:	n/a
4	chr14:72398839-72398889	IMR90	lung:	fetal
5	chr14:72398920-72398970	AG10803	skin:	n/a
6	chr14:72399809-72399859	MCF10A-Er-Src	breast:	n/a
7	chr14:72398920-72398970	NH-A	brain:	n/a
8	chr14:72400075-72400125	PFSK-1	brain:	n/a
9	chr14:72400075-72400125	HCPEpiC	choroid plexus:	n/a
10	chr14:72400168-72400218	SK-N-SH	brain:	n/a
11	chr14:72399846-72399896	RPTEC	kidney:	n/a
12	chr14:72400168-72400218	CMK	blood:	n/a
13	chr14:72398839-72398889	GM19239	blood:	n/a
14	chr14:72400168-72400218	NHDF-neo	bronchial:	n/a
15	chr14:72398856-72398906	NT2-D1	testis:	n/a
16	chr14:72399809-72399859	GM06990	blood:	n/a
17	chr14:72398856-72398906	U87	brain:	n/a
18	chr14:72398856-72398906	PrEC	prostate:	n/a
19	chr14:72399553-72399603	SK-N-MC	brain:	n/a
20	chr14:72399809-72399859	BE2_C	brain:	n/a
21	chr14:72400075-72400125	LNCaP	prostate:	n/a
22	chr14:72398856-72398906	AoSMC	blood vessel:	n/a
23	chr14:72398856-72398906	HIPEpiC	eye:	n/a
24	chr14:72399591-72399641	AG10803	skin:	n/a
25	chr14:72399809-72399859	HepG2	liver:	n/a
26	chr14:72398856-72398906	A549	lung:	n/a
27	chr14:72399553-72399603	HIPEpiC	eye:	n/a
28	chr14:72400168-72400218	AG04449	skin:	fetal
29	chr14:72398920-72398970	AG04450	lung:	fetal
30	chr14:72398839-72398889	ECC-1	luminal epithelium:	n/a
31	chr14:72399809-72399859	NH-A	brain:	n/a
32	chr14:72398839-72398889	HCT-116	colon:	n/a
33	chr14:72399846-72399896	HRPEpiC	eye:	n/a
34	chr14:72399553-72399603	GM12891	blood:	n/a
35	chr14:72399553-72399603	HRE	kidney:	n/a
36	chr14:72399553-72399603	AoSMC	blood vessel:	n/a
37	chr14:72398856-72398906	NB4	blood:	n/a
38	chr14:72399553-72399603	BJ	skin:	n/a
39	chr14:72399553-72399603	HRCEpiC	kidney:	n/a
40	chr14:72399809-72399859	HEEpiC	esophagus:	n/a
41	chr14:72399846-72399896	K562	blood:	n/a
42	chr14:72400075-72400125	AG09319	gingival:	n/a
43	chr14:72400168-72400218	IMR90	lung:	fetal
44	chr14:72400168-72400218	HL-60	blood:	n/a
45	chr14:72399553-72399603	HCT-116	colon:	n/a
46	chr14:72399846-72399896	HCPEpiC	choroid plexus:	n/a
47	chr14:72400168-72400218	HPAEpiC	pulmonary alveolar:	n/a
48	chr14:72398856-72398906	GM12878	blood:	n/a
49	chr14:72398839-72398889	T-47D	breast:	n/a
50	chr14:72400075-72400125	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:72398495..72399195-chr14:72887196..72888373,4	MCF-7	breast:
2	chr14:72400385..72403304-chr14:72425307..72428044,2	MCF-7	breast:

Variant related genes	Relation type
RGS6	TF binding region
RGS6	CpG island
ENSG00000182732	chromatin interactions

Extended variants
information (count: 80 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533328846	chr14:72397748-72397749	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs537091892	chr14:72397805-72397806	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs36325	chr14:72397853-72397854	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs374898782	chr14:72397889-72397890	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs139894366	chr14:72397920-72397921	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs2239270	chr14:72397948-72397949	Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs552966421	chr14:72397967-72397968	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs577785811	chr14:72397996-72397997	Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs185894496	chr14:72398070-72398071	Bivalent/Poised TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs545582255	chr14:72398101-72398102	Bivalent/Poised TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs563946672	chr14:72398164-72398165	Bivalent/Poised TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs370669381	chr14:72398197-72398198	Bivalent/Poised TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538442375	chr14:72398219-72398220	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs139386713	chr14:72398243-72398244	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs79676730	chr14:72398279-72398280	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs576116663	chr14:72398299-72398300	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs117574428	chr14:72398319-72398320	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs375169275	chr14:72398375-72398376	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs190070747	chr14:72398396-72398397	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs573669494	chr14:72398438-72398439	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs541724983	chr14:72398447-72398448	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs559780013	chr14:72398463-72398464	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs528864057	chr14:72398476-72398477	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368419490	chr14:72398506-72398507	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs36324	chr14:72398547-72398548	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs74363496	chr14:72398579-72398580	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs77571731	chr14:72398580-72398581	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559174204	chr14:72398737-72398738	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551680478	chr14:72398790-72398791	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs36323	chr14:72398796-72398797	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372258755	chr14:72398813-72398814	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs36322	chr14:72398840-72398841	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs549054114	chr14:72398846-72398847	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567294337	chr14:72398880-72398881	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534290837	chr14:72398936-72398937	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149758213	chr14:72398942-72398943	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571444320	chr14:72399025-72399026	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528325417	chr14:72399031-72399032	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs183058573	chr14:72399036-72399037	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556884264	chr14:72399038-72399039	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs568663084	chr14:72399044-72399045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs77022468	chr14:72399224-72399225	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs555405570	chr14:72399233-72399234	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs573730937	chr14:72399259-72399260	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs541052176	chr14:72399270-72399271	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs36321	chr14:72399319-72399320	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs578184848	chr14:72399355-72399356	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs545634766	chr14:72399357-72399358	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs563880339	chr14:72399361-72399362	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs368854471	chr14:72399377-72399378	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72397800-72398600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:72398000-72398200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
3	chr14:72398000-72398200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
4	chr14:72398000-72398400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr14:72398000-72399600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
6	chr14:72398000-72400800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr14:72398200-72398400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
8	chr14:72398200-72398400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr14:72398200-72398600	Active TSS	Psoas Muscle	Psoas
10	chr14:72398200-72398800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
11	chr14:72398200-72399000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
12	chr14:72398400-72398600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
13	chr14:72398400-72398600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
14	chr14:72398400-72398600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
15	chr14:72398400-72398600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
16	chr14:72398400-72398600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
17	chr14:72398400-72398600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
18	chr14:72398400-72398600	Active TSS	Brain Angular Gyrus	brain
19	chr14:72398400-72398600	Bivalent Enhancer	Brain Germinal Matrix	brain
20	chr14:72398400-72398600	Flanking Active TSS	Brain Hippocampus Middle	brain
21	chr14:72398400-72398600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
22	chr14:72398400-72398600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
23	chr14:72398400-72398600	Bivalent Enhancer	Fetal Intestine Large	intestine
24	chr14:72398400-72398600	Bivalent Enhancer	Fetal Kidney	kidney
25	chr14:72398400-72398600	Bivalent Enhancer	Fetal Lung	lung
26	chr14:72398400-72398600	Bivalent Enhancer	Fetal Stomach	stomach
27	chr14:72398400-72398600	Flanking Bivalent TSS/Enh	A549	lung
28	chr14:72398400-72398800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
29	chr14:72398400-72398800	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
30	chr14:72398400-72399000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr14:72398400-72399400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
32	chr14:72398400-72399400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
33	chr14:72398400-72399400	Bivalent/Poised TSS	Fetal Brain Female	brain
34	chr14:72398400-72399600	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
35	chr14:72398400-72399600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
36	chr14:72398400-72399600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr14:72398400-72399600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr14:72398400-72400200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
39	chr14:72398400-72400200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
40	chr14:72398400-72400200	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr14:72398400-72400400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
42	chr14:72398400-72400400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
43	chr14:72398400-72400400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr14:72398400-72400400	Bivalent Enhancer	Liver	Liver
45	chr14:72398400-72401600	Active TSS	Right Atrium	heart
46	chr14:72398400-72401800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:72398600-72398800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr14:72398600-72398800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
49	chr14:72398600-72398800	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
50	chr14:72398600-72398800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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