Variant report

Variant	esv3380705
Chromosome Location	chr14:32668101-32670199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:32670008-32673683	HepG2	liver:	n/a	chr14:32671605-32671621
2	BCL11A	chr14:32669630-32669939	GM12878	blood:	n/a	n/a
3	BCL11A	chr14:32669710-32669932	GM12878	blood:	n/a	n/a
4	BCLAF1	chr14:32669546-32670099	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:32670022-32670071	A549	lung:	n/a	n/a
6	BHLHE40	chr14:32669994-32671863	HepG2	liver:	n/a	n/a
7	BHLHE40	chr14:32669588-32670359	GM12878	blood:	n/a	n/a
8	BRCA1	chr14:32670041-32670552	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr14:32670196-32670668	K562	blood:	n/a	n/a
10	CEBPB	chr14:32670038-32671540	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr14:32669633-32670995	GM12878	blood:	n/a	n/a
12	CREB1	chr14:32669939-32673704	HepG2	liver:	n/a	n/a
13	CUX1	chr14:32669557-32670402	GM12878	blood:	n/a	n/a
14	EBF1	chr14:32669658-32670424	GM12878	blood:	n/a	n/a
15	EP300	chr14:32669593-32670027	GM12878	blood:	n/a	chr14:32669822-32669836 chr14:32669828-32669842
16	EP300	chr14:32669630-32670433	GM12878	blood:	n/a	chr14:32669822-32669836 chr14:32669828-32669842
17	EP300	chr14:32669578-32670795	GM12878	blood:	n/a	chr14:32669822-32669836 chr14:32669828-32669842
18	FOXA2	chr14:32669929-32671226	HepG2	liver:	n/a	n/a
19	GTF2F1	chr14:32670109-32671364	Hela-S3	cervix:	n/a	n/a
20	HDAC2	chr14:32670112-32671645	MCF-7	breast:	n/a	chr14:32670545-32670564
21	HDAC2	chr14:32670163-32672953	HepG2	liver:	n/a	chr14:32671861-32671880 chr14:32670545-32670564
22	HDAC2	chr14:32670178-32670684	MCF-7	breast:	n/a	chr14:32670545-32670564
23	HDAC2	chr14:32670159-32671734	HepG2	liver:	n/a	chr14:32670545-32670564
24	HEY1	chr14:32669934-32671610	HepG2	liver:	n/a	n/a
25	HEY1	chr14:32669955-32671487	HepG2	liver:	n/a	n/a
26	HNF4A	chr14:32670119-32671566	HepG2	liver:	n/a	chr14:32670144-32670157 chr14:32670144-32670156 chr14:32670143-32670157 chr14:32670141-32670159 chr14:32670806-32670821 chr14:32670144-32670156 chr14:32670143-32670157 chr14:32670706-32670718 chr14:32670143-32670156 chr14:32670144-32670156
27	IKZF1	chr14:32669575-32670421	GM12878	blood:	n/a	n/a
28	IRF4	chr14:32669604-32670045	GM12878	blood:	n/a	n/a
29	KAP1	chr14:32670030-32673658	HEK293	kidney:	n/a	n/a
30	MAX	chr14:32670015-32671824	HepG2	liver:	n/a	n/a
31	MAX	chr14:32669914-32673720	HepG2	liver:	n/a	chr14:32672740-32672750
32	MAX	chr14:32669799-32673731	HepG2	liver:	n/a	chr14:32672740-32672750
33	MAX	chr14:32669930-32673856	A549	lung:	n/a	chr14:32672740-32672750
34	MAX	chr14:32669830-32671113	GM12878	blood:	n/a	n/a
35	MAX	chr14:32670013-32671791	A549	lung:	n/a	n/a
36	MAX	chr14:32670021-32671500	Hela-S3	cervix:	n/a	n/a
37	MAX	chr14:32670157-32671259	MCF-7	breast:	n/a	n/a
38	MAX	chr14:32670160-32671597	ECC-1	luminal epithelium:	n/a	n/a
39	MAZ	chr14:32670158-32671413	HepG2	liver:	n/a	n/a
40	MAZ	chr14:32669713-32670903	GM12878	blood:	n/a	n/a
41	MBD4	chr14:32669890-32673606	HepG2	liver:	n/a	n/a
42	MBD4	chr14:32669896-32673886	HepG2	liver:	n/a	n/a
43	MEF2A	chr14:32669669-32670001	GM12878	blood:	n/a	n/a
44	MEF2A	chr14:32669501-32670091	GM12878	blood:	n/a	n/a
45	MEF2C	chr14:32669587-32670068	GM12878	blood:	n/a	chr14:32669834-32669849
46	MXI1	chr14:32669629-32673720	SK-N-SH	brain:	n/a	n/a
47	MXI1	chr14:32670069-32673550	HepG2	liver:	n/a	n/a
48	MXI1	chr14:32669911-32671203	Hela-S3	cervix:	n/a	n/a
49	MXI1	chr14:32669569-32671039	GM12878	blood:	n/a	n/a
50	MYBL2	chr14:32669879-32673629	HepG2	liver:	n/a	n/a

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No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:32668091-32668141	NHDF-neo	bronchial:	n/a
2	chr14:32668091-32668141	Jurkat	blood:	n/a
3	chr14:32668091-32668141	GM12878	blood:	n/a
4	chr14:32668091-32668141	ECC-1	luminal epithelium:	n/a
5	chr14:32668091-32668141	HEK293	kidney:	embryo
6	chr14:32668091-32668141	MCF-7	breast:	n/a
7	chr14:32668091-32668141	Caco-2	colon:	n/a
8	chr14:32668091-32668141	Hepatocyte	liver:	n/a
9	chr14:32668091-32668141	T-47D	breast:	n/a
10	chr14:32668091-32668141	NB4	blood:	n/a
11	chr14:32668091-32668141	SK-N-SH	brain:	n/a
12	chr14:32668091-32668141	RPTEC	kidney:	n/a
13	chr14:32668091-32668141	AG04449	skin:	fetal
14	chr14:32668091-32668141	AoSMC	blood vessel:	n/a
15	chr14:32668091-32668141	HepG2	liver:	n/a
16	chr14:32668091-32668141	GM06990	blood:	n/a
17	chr14:32668091-32668141	BE2_C	brain:	n/a
18	chr14:32668091-32668141	IMR90	lung:	fetal
19	chr14:32668091-32668141	HIPEpiC	eye:	n/a
20	chr14:32668091-32668141	HNPCEpiC	eye:	n/a
21	chr14:32668091-32668141	CMK	blood:	n/a
22	chr14:32668091-32668141	HL-60	blood:	n/a
23	chr14:32668091-32668141	AG09309	skin:	n/a
24	chr14:32668091-32668141	PANC-1	pancreas:	n/a
25	chr14:32668091-32668141	HPAEpiC	pulmonary alveolar:	n/a
26	chr14:32668091-32668141	A549	lung:	n/a
27	chr14:32668091-32668141	NT2-D1	testis:	n/a
28	chr14:32668091-32668141	HCT-116	colon:	n/a
29	chr14:32668091-32668141	ovcar-3	ovarian:	n/a
30	chr14:32668091-32668141	AG09319	gingival:	n/a
31	chr14:32668091-32668141	U87	brain:	n/a
32	chr14:32668091-32668141	SKMC	muscle:	n/a
33	chr14:32668091-32668141	H1-hESC	embryonic stem cell:	embryo
34	chr14:32668091-32668141	SK-N-SH_RA	brain:	n/a
35	chr14:32668091-32668141	HCM	heart:	n/a
36	chr14:32668091-32668141	HCF	heart:	n/a
37	chr14:32668091-32668141	LNCaP	prostate:	n/a
38	chr14:32668091-32668141	AG04450	lung:	fetal
39	chr14:32668091-32668141	NH-A	brain:	n/a
40	chr14:32668091-32668141	BJ	skin:	n/a
41	chr14:32668091-32668141	NHBE	bronchial:	n/a
42	chr14:32668091-32668141	HAEpiC	amniotic membrane:	n/a
43	chr14:32668091-32668141	PFSK-1	brain:	n/a
44	chr14:32668091-32668141	PrEC	prostate:	n/a
45	chr14:32668091-32668141	AG10803	skin:	n/a
46	chr14:32668091-32668141	HRCEpiC	kidney:	n/a
47	chr14:32668091-32668141	HMEC	breast:	n/a
48	chr14:32668091-32668141	GM12891	blood:	n/a
49	chr14:32668091-32668141	HRE	kidney:	n/a
50	chr14:32668091-32668141	HCPEpiC	choroid plexus:	n/a

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No.	Distal block	Cell Line	Cell type
1	chr14:32544500..32547770-chr14:32669959..32673759,8	K562	blood:
2	chr14:32665295..32667033-chr14:32668377..32670750,3	K562	blood:
3	chr14:32544948..32548496-chr14:32669195..32673537,9	MCF-7	breast:
4	chr14:32544618..32548147-chr14:32668083..32673759,9	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf126-5	chr14:32669704-32670732	XLOC_010989

No data

Variant related genes	Relation type
RNU6-7	TF binding region
RNU6-7	CpG island
ENSG00000258655	chromatin interactions
ENSG00000100852	chromatin interactions

Extended variants
information (count: 72 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:72 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534335286	chr14:32668123-32668124	Weak transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs140072741	chr14:32668145-32668146	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs572281249	chr14:32668186-32668187	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs536427454	chr14:32668316-32668317	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs574006870	chr14:32668318-32668319	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs554778592	chr14:32668326-32668327	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs375590351	chr14:32668346-32668347	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs534836237	chr14:32668372-32668373	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149919650	chr14:32668373-32668374	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs200638894	chr14:32668378-32668379	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371953462	chr14:32668380-32668381	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs200580927	chr14:32668383-32668384	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs544594941	chr14:32668384-32668385	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs189910260	chr14:32668386-32668387	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577932539	chr14:32668403-32668404	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs150073278	chr14:32668460-32668461	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560341065	chr14:32668530-32668531	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs558950583	chr14:32668532-32668533	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs150717332	chr14:32668539-32668540	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs71115051	chr14:32668540-32668541	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs527871950	chr14:32668546-32668547	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs143679496	chr14:32668549-32668550	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs549271618	chr14:32668565-32668566	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561041271	chr14:32668761-32668762	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201306780	chr14:32668773-32668774	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs367844218	chr14:32668774-32668775	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs1958368	chr14:32668784-32668785	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs11845779	chr14:32668786-32668787	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181417179	chr14:32668821-32668822	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs148404583	chr14:32668850-32668851	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112143503	chr14:32668875-32668876	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs5002692	chr14:32668899-32668900	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565920736	chr14:32668900-32668901	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201925216	chr14:32668928-32668929	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554418526	chr14:32668960-32668961	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372762958	chr14:32668993-32668994	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs375958463	chr14:32668999-32669000	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs372692188	chr14:32669001-32669002	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs6145289	chr14:32669009-32669010	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs3030510	chr14:32669016-32669017	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs373071019	chr14:32669023-32669024	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567769052	chr14:32669077-32669078	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs537918308	chr14:32669079-32669080	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371608980	chr14:32669080-32669081	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs142496722	chr14:32669101-32669102	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs549281472	chr14:32669111-32669112	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs115453833	chr14:32669123-32669124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs545336878	chr14:32669128-32669129	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185239875	chr14:32669134-32669135	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs146417378	chr14:32669287-32669288	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	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
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32660200-32669000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr14:32667600-32670000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:32667600-32670000	Weak transcription	NHEK	skin
4	chr14:32668000-32669200	Weak transcription	GM12878-XiMat	blood
5	chr14:32668400-32668600	Enhancers	Fetal Intestine Small	intestine
6	chr14:32668600-32669800	Weak transcription	Fetal Intestine Small	intestine
7	chr14:32669000-32669200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:32669000-32669600	Enhancers	Primary B cells from cord blood	blood
9	chr14:32669000-32669800	Enhancers	Primary B cells from peripheral blood	blood
10	chr14:32669200-32669400	Enhancers	Primary hematopoietic stem cells	blood
11	chr14:32669200-32669400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr14:32669200-32669400	Enhancers	GM12878-XiMat	blood
13	chr14:32669200-32669600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr14:32669200-32669800	Enhancers	Liver	Liver
15	chr14:32669200-32669800	Enhancers	Hela-S3	cervix
16	chr14:32669200-32669800	Flanking Active TSS	HepG2	liver
17	chr14:32669200-32669800	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr14:32669200-32670000	Enhancers	Adipose Nuclei	Adipose
19	chr14:32669200-32672400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:32669400-32669600	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr14:32669400-32669800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr14:32669400-32669800	Enhancers	Duodenum Mucosa	Duodenum
23	chr14:32669400-32670000	Flanking Active TSS	GM12878-XiMat	blood
24	chr14:32669400-32671600	Active TSS	A549	lung
25	chr14:32669400-32672400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr14:32669400-32673600	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr14:32669600-32669800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:32669600-32669800	Enhancers	Primary T cells from cord blood	blood
29	chr14:32669600-32669800	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr14:32669600-32669800	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr14:32669600-32669800	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr14:32669600-32669800	Enhancers	Brain Hippocampus Middle	brain
33	chr14:32669600-32670000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr14:32669600-32670000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr14:32669600-32670200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
36	chr14:32669600-32672400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:32669600-32673600	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr14:32669600-32674000	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr14:32669800-32670000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr14:32669800-32670000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr14:32669800-32670000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
42	chr14:32669800-32670000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
43	chr14:32669800-32670000	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr14:32669800-32670000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr14:32669800-32670000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr14:32669800-32670000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr14:32669800-32670000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr14:32669800-32670000	Flanking Active TSS	Liver	Liver
49	chr14:32669800-32670000	Enhancers	Fetal Intestine Small	intestine
50	chr14:32669800-32670000	Active TSS	Fetal Lung	lung

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