Variant report

Variant	nsv974314
Chromosome Location	chr14:21679868-21701353
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:646)
CpG islands
(count:61)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21697647-21697673	K562	blood:	n/a	n/a
2	BRCA1	chr14:21699415-21699501	GM12878	blood:	n/a	n/a
3	CEBPB	chr14:21699397-21699763	IMR90	lung:	n/a	chr14:21699571-21699582
4	CEBPB	chr14:21699413-21699749	HepG2	liver:	n/a	chr14:21699571-21699582
5	CEBPB	chr14:21699408-21699718	K562	blood:	n/a	chr14:21699571-21699582
6	CEBPB	chr14:21686243-21686651	Hela-S3	cervix:	n/a	chr14:21686525-21686538 chr14:21686494-21686506
7	CEBPB	chr14:21699392-21699707	A549	lung:	n/a	chr14:21699571-21699582
8	CEBPB	chr14:21686197-21686719	MCF-7	breast:	n/a	chr14:21686525-21686538 chr14:21686494-21686506
9	CEBPB	chr14:21686274-21686500	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:21699301-21699819	A549	lung:	n/a	chr14:21699571-21699582
11	CEBPB	chr14:21686264-21686529	A549	lung:	n/a	chr14:21686494-21686506
12	CEBPB	chr14:21699339-21699811	MCF-7	breast:	n/a	chr14:21699571-21699582
13	CEBPB	chr14:21698112-21698459	A549	lung:	n/a	n/a
14	CEBPB	chr14:21699396-21699731	Hela-S3	cervix:	n/a	chr14:21699571-21699582
15	CEBPB	chr14:21686238-21687069	IMR90	lung:	n/a	chr14:21686525-21686538 chr14:21686494-21686506
16	CTCF	chr14:21686320-21686470	HepG2	liver:	n/a	n/a
17	CTCF	chr14:21685540-21685690	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr14:21686300-21686450	GM12865	blood:	n/a	n/a
19	CTCF	chr14:21686372-21686389	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:21686260-21686410	GM12871	blood:	n/a	n/a
21	CTCF	chr14:21686280-21686430	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:21685480-21685630	HMF	breast:	n/a	n/a
23	CTCF	chr14:21686380-21686530	GM12866	blood:	n/a	n/a
24	CTCF	chr14:21686340-21686490	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr14:21691920-21692070	HVMF	connective:	n/a	n/a
26	E2F4	chr14:21686359-21686522	MCF10A-Er-Src	breast:	n/a	n/a
27	EP300	chr14:21686218-21686691	SK-N-SH	brain:	n/a	n/a
28	FOS	chr14:21686252-21686936	MCF10A-Er-Src	breast:	n/a	chr14:21686874-21686882
29	FOS	chr14:21686256-21686620	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr14:21699517-21699606	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr14:21686233-21686596	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr14:21686866-21686895	MCF10A-Er-Src	breast:	n/a	chr14:21686874-21686882
33	FOS	chr14:21684386-21684389	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr14:21686232-21686628	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr14:21689370-21689541	MCF10A-Er-Src	breast:	n/a	chr14:21689415-21689424
36	FOS	chr14:21689288-21689488	MCF10A-Er-Src	breast:	n/a	chr14:21689415-21689424
37	FOSL2	chr14:21686213-21686668	A549	lung:	n/a	n/a
38	FOSL2	chr14:21686231-21686580	HepG2	liver:	n/a	n/a
39	FOSL2	chr14:21686186-21686668	MCF-7	breast:	n/a	n/a
40	FOSL2	chr14:21686128-21686662	SK-N-SH	brain:	n/a	n/a
41	FOXA1	chr14:21688566-21688829	T-47D	breast:	n/a	n/a
42	GATA2	chr14:21686254-21686830	HUVEC	blood vessel:	n/a	n/a
43	GATA3	chr14:21686193-21686942	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr14:21686312-21686599	MCF-7	breast:	n/a	n/a
45	GATA3	chr14:21686070-21686770	A549	lung:	n/a	n/a
46	GATA3	chr14:21686104-21686891	MCF-7	breast:	n/a	n/a
47	GATA3	chr14:21686335-21686539	T-47D	breast:	n/a	n/a
48	GATA3	chr14:21686075-21686847	SK-N-SH	brain:	n/a	n/a
49	GATA3	chr14:21686088-21686905	MCF-7	breast:	n/a	n/a
50	GATA3	chr14:21695560-21695904	SH-SY5Y	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21689119-21689169	ProgFib	skin:	n/a
2	chr14:21689119-21689169	PANC-1	pancreas:	n/a
3	chr14:21689119-21689169	NHBE	bronchial:	n/a
4	chr14:21689119-21689169	CMK	blood:	n/a
5	chr14:21689119-21689169	SK-N-MC	brain:	n/a
6	chr14:21689119-21689169	AG10803	skin:	n/a
7	chr14:21689119-21689169	HRCEpiC	kidney:	n/a
8	chr14:21689119-21689169	BE2_C	brain:	n/a
9	chr14:21689119-21689169	HL-60	blood:	n/a
10	chr14:21689119-21689169	Jurkat	blood:	n/a
11	chr14:21689119-21689169	HIPEpiC	eye:	n/a
12	chr14:21689119-21689169	AG04449	skin:	fetal
13	chr14:21689119-21689169	NHDF-neo	bronchial:	n/a
14	chr14:21689119-21689169	SKMC	muscle:	n/a
15	chr14:21689119-21689169	U87	brain:	n/a
16	chr14:21689119-21689169	Caco-2	colon:	n/a
17	chr14:21689119-21689169	AG04450	lung:	fetal
18	chr14:21689119-21689169	HUVEC	blood vessel:	n/a
19	chr14:21689119-21689169	PFSK-1	brain:	n/a
20	chr14:21689119-21689169	MCF10A-Er-Src	breast:	n/a
21	chr14:21689119-21689169	HAEpiC	amniotic membrane:	n/a
22	chr14:21689119-21689169	HCPEpiC	choroid plexus:	n/a
23	chr14:21689119-21689169	HCF	heart:	n/a
24	chr14:21689119-21689169	GM19239	blood:	n/a
25	chr14:21689119-21689169	RPTEC	kidney:	n/a
26	chr14:21689119-21689169	HCM	heart:	n/a
27	chr14:21689119-21689169	Hela-S3	cervix:	n/a
28	chr14:21689119-21689169	HRPEpiC	eye:	n/a
29	chr14:21689119-21689169	HMEC	breast:	n/a
30	chr14:21689119-21689169	AG09309	skin:	n/a
31	chr14:21689119-21689169	GM06990	blood:	n/a
32	chr14:21689119-21689169	Hepatocyte	liver:	n/a
33	chr14:21689119-21689169	HEEpiC	esophagus:	n/a
34	chr14:21689119-21689169	HRE	kidney:	n/a
35	chr14:21689119-21689169	GM12891	blood:	n/a
36	chr14:21689119-21689169	HNPCEpiC	eye:	n/a
37	chr14:21689119-21689169	IMR90	lung:	fetal
38	chr14:21689119-21689169	LNCaP	prostate:	n/a
39	chr14:21689119-21689169	SK-N-SH_RA	brain:	n/a
40	chr14:21689119-21689169	A549	lung:	n/a
41	chr14:21689119-21689169	MCF-7	breast:	n/a
42	chr14:21689119-21689169	NT2-D1	testis:	n/a
43	chr14:21689119-21689169	SK-N-SH	brain:	n/a
44	chr14:21689119-21689169	AG09319	gingival:	n/a
45	chr14:21689119-21689169	ovcar-3	ovarian:	n/a
46	chr14:21689119-21689169	HEK293	kidney:	embryo
47	chr14:21689119-21689169	H1-hESC	embryonic stem cell:	embryo
48	chr14:21689119-21689169	NH-A	brain:	n/a
49	chr14:21689119-21689169	BJ	skin:	n/a
50	chr14:21689119-21689169	GM12892	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21694684..21697867-chr14:21700846..21706348,4	MCF-7	breast:
2	chr14:21671465..21674942-chr14:21676988..21681110,7	MCF-7	breast:
3	chr14:21692662..21694223-chr14:21694596..21696164,2	MCF-7	breast:
4	chr14:21689000..21691268-chr14:21851211..21853511,2	MCF-7	breast:
5	chr14:21693897..21696287-chr14:21697693..21699840,2	MCF-7	breast:
6	chr14:21694684..21697867-chr14:21700846..21706348,4	MCF-7	breast:
7	chr14:21688131..21691193-chr14:21736092..21738684,3	MCF-7	breast:
8	chr14:21691458..21693876-chr14:21698799..21700473,3	K562	blood:
9	chr14:21684971..21687405-chr14:21736664..21738674,3	MCF-7	breast:
10	chr14:21682936..21686679-chr14:21688141..21690652,4	K562	blood:
11	chr14:21679501..21682581-chr14:21683492..21686432,4	K562	blood:
12	chr14:21698033..21699942-chr14:21736432..21738329,2	MCF-7	breast:
13	chr14:21689585..21692266-chr14:21692375..21695207,2	MCF-7	breast:
14	chr14:21683942..21686435-chr14:21849185..21850784,2	MCF-7	breast:
15	chr14:21678068..21679716-chr14:21682875..21685617,2	K562	blood:
16	chr14:21679834..21681471-chr14:21683651..21685737,2	K562	blood:
17	chr14:21700378..21702346-chr14:21819126..21821504,2	MCF-7	breast:
18	chr14:21682920..21686919-chr14:21693629..21695651,3	MCF-7	breast:
19	chr14:21682936..21686679-chr14:21688141..21690652,4	K562	blood:
20	chr14:21687620..21689527-chr14:21733855..21735500,2	MCF-7	breast:
21	chr14:21680490..21682250-chr14:21684658..21687310,2	MCF-7	breast:
22	chr14:21690598..21692490-chr14:21705492..21708066,2	MCF-7	breast:
23	chr14:21692662..21694223-chr14:21694596..21696164,2	MCF-7	breast:
24	chr14:21680608..21683274-chr14:21683890..21685747,2	MCF-7	breast:
25	chr14:21701295..21703897-chr14:21842847..21844816,2	K562	blood:
26	chr14:21689585..21692266-chr14:21692375..21695207,2	MCF-7	breast:
27	chr14:21682920..21686919-chr14:21693629..21695651,3	MCF-7	breast:
28	chr14:21682890..21684914-chr14:21686115..21687924,2	K562	blood:
29	chr14:21682890..21684914-chr14:21686115..21687924,2	K562	blood:
30	chr14:21678499..21681454-chr14:21736107..21737906,2	MCF-7	breast:
31	chr14:21692516..21695452-chr14:21813712..21815448,2	MCF-7	breast:
32	chr14:21700872..21703141-chr14:21723886..21726612,2	K562	blood:

No data

Variant related genes	Relation type
LINC00641	TF binding region
HNRNPC	TF binding region
LINC00641	CpG island
HNRNPC	CpG island
ENSG00000260830	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000092201	chromatin interactions
ENSG00000258441	chromatin interactions

Extended variants
information (count: 953 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562137788	chr14:21679893-21679894	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs181996289	chr14:21679907-21679908	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs535014388	chr14:21679916-21679917	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs551439313	chr14:21679919-21679920	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs199851959	chr14:21679929-21679930	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs184224993	chr14:21679940-21679941	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372018302	chr14:21679964-21679965	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs201491227	chr14:21679970-21679971	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs17856245	chr14:21679973-21679974	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs199818734	chr14:21679980-21679981	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs371315588	chr14:21680017-21680018	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs143915763	chr14:21680061-21680062	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs148641628	chr14:21680109-21680110	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs145536390	chr14:21680123-21680124	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs553623551	chr14:21680159-21680160	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573507975	chr14:21680166-21680167	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs545689589	chr14:21680172-21680173	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs147726137	chr14:21680215-21680216	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs141018174	chr14:21680216-21680217	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs574679946	chr14:21680238-21680239	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs543519945	chr14:21680239-21680240	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs559779676	chr14:21680260-21680261	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs144966167	chr14:21680290-21680291	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs529089521	chr14:21680316-21680317	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs76386361	chr14:21680327-21680328	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs559501842	chr14:21680348-21680349	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs372545350	chr14:21680384-21680385	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs574767002	chr14:21680397-21680398	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs573920333	chr14:21680411-21680412	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs114286876	chr14:21680417-21680418	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs551671747	chr14:21680419-21680420	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs12433590	chr14:21680424-21680425	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs530841243	chr14:21680439-21680440	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs564009094	chr14:21680451-21680452	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs369658240	chr14:21680455-21680456	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs118190136	chr14:21680458-21680459	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs200673309	chr14:21680524-21680525	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs536448162	chr14:21680552-21680553	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs531203149	chr14:21680586-21680587	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs553246348	chr14:21680670-21680671	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs151328216	chr14:21680700-21680701	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs538932952	chr14:21680708-21680709	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs77823834	chr14:21680716-21680717	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs190086240	chr14:21680717-21680718	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs577693287	chr14:21680751-21680752	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs181110770	chr14:21680754-21680755	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs557089499	chr14:21680790-21680791	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs372991204	chr14:21680848-21680849	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs375325184	chr14:21680852-21680853	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs573731835	chr14:21680865-21680866	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	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
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21660600-21686200	Weak transcription	Right Atrium	heart
2	chr14:21669000-21685800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr14:21669400-21681600	Strong transcription	Left Ventricle	heart
4	chr14:21669400-21685600	Strong transcription	Muscle Satellite Cultured Cells	--
5	chr14:21670000-21681600	Strong transcription	Fetal Muscle Leg	muscle
6	chr14:21670200-21683600	Strong transcription	Fetal Thymus	thymus
7	chr14:21670200-21684200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:21670200-21684600	Strong transcription	NHLF	lung
9	chr14:21670200-21685000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr14:21670200-21685400	Strong transcription	HSMM	muscle
11	chr14:21670200-21685400	Strong transcription	NH-A	brain
12	chr14:21670200-21685400	Strong transcription	Osteobl	bone
13	chr14:21670400-21697600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:21670600-21683400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:21670800-21682400	Strong transcription	A549	lung
16	chr14:21670800-21684800	Strong transcription	HSMMtube	muscle
17	chr14:21670800-21685000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr14:21670800-21687400	Strong transcription	Fetal Brain Female	brain
19	chr14:21670800-21702400	Strong transcription	Fetal Muscle Trunk	muscle
20	chr14:21671200-21732000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr14:21671400-21681000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr14:21671400-21684600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr14:21671400-21684800	Strong transcription	Stomach Smooth Muscle	stomach
24	chr14:21671600-21681600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr14:21671600-21682800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr14:21671600-21686000	Strong transcription	HUVEC	blood vessel
27	chr14:21671600-21688200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr14:21671800-21683600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr14:21672200-21680000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr14:21672200-21684200	Strong transcription	HMEC	breast
31	chr14:21672200-21696600	Strong transcription	Primary B cells from cord blood	blood
32	chr14:21672400-21680000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr14:21672400-21680800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr14:21672400-21684800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
35	chr14:21672400-21696000	Strong transcription	Adipose Nuclei	Adipose
36	chr14:21672400-21709000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr14:21672600-21683600	Strong transcription	NHEK	skin
38	chr14:21672600-21685400	Strong transcription	NHDF-Ad	bronchial
39	chr14:21672600-21703000	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr14:21672800-21681400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr14:21672800-21682400	Strong transcription	Primary T cells from cord blood	blood
42	chr14:21672800-21682400	Strong transcription	Brain Anterior Caudate	brain
43	chr14:21672800-21682600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr14:21672800-21684400	Strong transcription	Placenta	Placenta
45	chr14:21672800-21685800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:21672800-21699400	Strong transcription	Duodenum Mucosa	Duodenum
47	chr14:21672800-21699400	Strong transcription	Rectal Mucosa Donor 29	rectum
48	chr14:21672800-21709000	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr14:21672800-21725200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr14:21673000-21681400	Strong transcription	Sigmoid Colon	Sigmoid Colon

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