Variant report

Variant	nsv85879
Chromosome Location	chr14:21965690-21974198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:475)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21966671-21967139	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:21966738-21967030	K562	blood:	n/a	n/a
3	ATF2	chr14:21973180-21973706	GM12878	blood:	n/a	n/a
4	BHLHE40	chr14:21967433-21967646	GM12878	blood:	n/a	n/a
5	BRCA1	chr14:21971560-21971576	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:21966060-21966384	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:21970169-21970287	A549	lung:	n/a	chr14:21970212-21970223
8	CEBPB	chr14:21970141-21970375	HepG2	liver:	n/a	chr14:21970212-21970223
9	CEBPB	chr14:21966244-21966249	K562	blood:	n/a	n/a
10	CTCF	chr14:21966800-21966950	AG04450	lung:	n/a	n/a
11	CTCF	chr14:21966820-21966970	HA-sp	spinal cord:	n/a	n/a
12	CTCF	chr14:21966800-21966950	GM12867	blood:	n/a	n/a
13	CTCF	chr14:21966800-21966950	SAEC	small airway:	n/a	n/a
14	CTCF	chr14:21966759-21967017	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr14:21966800-21966950	GM12878	blood:	n/a	n/a
16	CTCF	chr14:21966659-21967113	A549	lung:	n/a	n/a
17	CTCF	chr14:21966722-21967031	A549	lung:	n/a	n/a
18	CTCF	chr14:21966742-21966934	A549	lung:	n/a	n/a
19	CTCF	chr14:21966820-21966970	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr14:21966800-21966950	GM06990	blood:	n/a	n/a
21	CTCF	chr14:21966800-21966950	Caco-2	colon:	n/a	n/a
22	CTCF	chr14:21966800-21966950	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr14:21966740-21966890	AG04450	lung:	n/a	n/a
24	CTCF	chr14:21966840-21966990	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr14:21966800-21966950	BJ	skin:	n/a	n/a
26	CTCF	chr14:21966734-21966979	GM13977	blood:	n/a	n/a
27	CTCF	chr14:21966820-21966970	GM12873	blood:	n/a	n/a
28	CTCF	chr14:21966840-21966990	HAc	cerebellar:	n/a	n/a
29	CTCF	chr14:21966820-21966970	GM12875	blood:	n/a	n/a
30	CTCF	chr14:21966780-21966930	HepG2	liver:	n/a	n/a
31	CTCF	chr14:21966840-21966990	HCT-116	colon:	n/a	n/a
32	CTCF	chr14:21966820-21966970	NHEK	skin:	n/a	n/a
33	CTCF	chr14:21966800-21966950	AG09309	skin:	n/a	n/a
34	CTCF	chr14:21966800-21966950	HAc	cerebellar:	n/a	n/a
35	CTCF	chr14:21966760-21966910	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr14:21966860-21967010	GM12874	blood:	n/a	n/a
37	CTCF	chr14:21966774-21966985	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr14:21966800-21966950	GM12874	blood:	n/a	n/a
39	CTCF	chr14:21966820-21966970	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:21966786-21966993	Lung_OC	lung:	n/a	n/a
41	CTCF	chr14:21966800-21966950	HEK293	kidney:	n/a	n/a
42	CTCF	chr14:21966800-21966950	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr14:21966740-21967016	Medullo	brain:	n/a	n/a
44	CTCF	chr14:21966780-21966930	GM12871	blood:	n/a	n/a
45	CTCF	chr14:21966840-21966990	HVMF	connective:	n/a	n/a
46	CTCF	chr14:21966820-21966970	BJ	skin:	n/a	n/a
47	CTCF	chr14:21966554-21966597	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr14:21967060-21967210	GM12866	blood:	n/a	n/a
49	CTCF	chr14:21966437-21967295	SK-N-SH	brain:	n/a	n/a
50	CTCF	chr14:21966840-21966990	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21966454-21966504	Hela-S3	cervix:	n/a
2	chr14:21966454-21966504	AG10803	skin:	n/a
3	chr14:21966454-21966504	SKMC	muscle:	n/a
4	chr14:21966454-21966504	HPAEpiC	pulmonary alveolar:	n/a
5	chr14:21966454-21966504	SK-N-SH	brain:	n/a
6	chr14:21966454-21966504	AG09319	gingival:	n/a
7	chr14:21966454-21966504	HCPEpiC	choroid plexus:	n/a
8	chr14:21966454-21966504	SK-N-MC	brain:	n/a
9	chr14:21966454-21966504	MCF-7	breast:	n/a
10	chr14:21966454-21966504	Jurkat	blood:	n/a
11	chr14:21966454-21966504	SAEC	small airway:	n/a
12	chr14:21966454-21966504	PFSK-1	brain:	n/a
13	chr14:21966454-21966504	HIPEpiC	eye:	n/a
14	chr14:21966454-21966504	PrEC	prostate:	n/a
15	chr14:21966454-21966504	HEEpiC	esophagus:	n/a
16	chr14:21966454-21966504	HRE	kidney:	n/a
17	chr14:21966454-21966504	CMK	blood:	n/a
18	chr14:21966454-21966504	NHDF-neo	bronchial:	n/a
19	chr14:21966454-21966504	Caco-2	colon:	n/a
20	chr14:21966454-21966504	ovcar-3	ovarian:	n/a
21	chr14:21966454-21966504	ECC-1	luminal epithelium:	n/a
22	chr14:21966454-21966504	HEK293	kidney:	embryo
23	chr14:21966454-21966504	Hepatocyte	liver:	n/a
24	chr14:21966454-21966504	NHBE	bronchial:	n/a
25	chr14:21966454-21966504	AoSMC	blood vessel:	n/a
26	chr14:21966454-21966504	K562	blood:	n/a
27	chr14:21966454-21966504	ProgFib	skin:	n/a
28	chr14:21966454-21966504	HNPCEpiC	eye:	n/a
29	chr14:21966454-21966504	HUVEC	blood vessel:	n/a
30	chr14:21966454-21966504	HRPEpiC	eye:	n/a
31	chr14:21966454-21966504	GM19239	blood:	n/a
32	chr14:21966454-21966504	A549	lung:	n/a
33	chr14:21966454-21966504	GM12891	blood:	n/a
34	chr14:21966454-21966504	LNCaP	prostate:	n/a
35	chr14:21966454-21966504	HAEpiC	amniotic membrane:	n/a
36	chr14:21966454-21966504	RPTEC	kidney:	n/a
37	chr14:21966454-21966504	NH-A	brain:	n/a
38	chr14:21966454-21966504	PANC-1	pancreas:	n/a
39	chr14:21966454-21966504	SK-N-SH_RA	brain:	n/a
40	chr14:21966454-21966504	AG04450	lung:	fetal
41	chr14:21966454-21966504	HepG2	liver:	n/a
42	chr14:21966454-21966504	HCM	heart:	n/a
43	chr14:21966454-21966504	GM12892	blood:	n/a
44	chr14:21966454-21966504	AG04449	skin:	fetal
45	chr14:21966454-21966504	T-47D	breast:	n/a
46	chr14:21966454-21966504	GM06990	blood:	n/a
47	chr14:21966454-21966504	IMR90	lung:	fetal
48	chr14:21966454-21966504	HCT-116	colon:	n/a
49	chr14:21966454-21966504	BE2_C	brain:	n/a
50	chr14:21966454-21966504	NB4	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21965159..21967752-chr14:22024395..22027094,3	MCF-7	breast:
2	chr14:21969916..21972018-chr14:21978032..21980758,3	K562	blood:
3	chr14:21966429..21967420-chr14:22025503..22026403,9	K562	blood:
4	chr14:21965602..21968556-chr14:21970950..21973416,3	K562	blood:
5	chr14:21968819..21970753-chr14:21994142..21996626,2	K562	blood:
6	chr14:21966403..21967388-chr14:22025432..22026169,5	MCF-7	breast:
7	chr14:21967474..21971361-chr14:22024015..22027387,4	K562	blood:
8	chr14:21973399..21975434-chr14:22010976..22012541,2	K562	blood:
9	chr14:21935572..21937160-chr14:21965846..21967879,2	MCF-7	breast:
10	chr14:21924252..21925871-chr14:21972693..21974391,2	MCF-7	breast:
11	chr14:21973675..21975896-chr14:22025670..22027377,2	K562	blood:
12	chr14:21966582..21968425-chr14:21990390..21992940,3	K562	blood:
13	chr14:21966153..21966705-chr20:52556158..52557026,2	MCF-7	breast:
14	chr14:21944053..21946667-chr14:21973536..21975748,2	MCF-7	breast:
15	chr14:21944239..21947571-chr14:21970430..21973821,4	MCF-7	breast:
16	chr14:21966135..21967334-chr14:22024735..22026336,7	MCF-7	breast:
17	chr14:21972318..21975113-chr14:21978008..21980143,3	K562	blood:
18	chr14:21964090..21967088-chr14:22024145..22025808,2	K562	blood:
19	chr14:21965763..21969009-chr14:21976812..21979865,4	K562	blood:
20	chr14:21966391..21966954-chr14:21994368..21995242,2	K562	blood:
21	chr14:21851876..21853838-chr14:21970156..21972342,2	MCF-7	breast:
22	chr14:21922971..21924665-chr14:21973742..21975845,3	MCF-7	breast:
23	chr14:21965103..21966895-chr14:22024708..22027624,2	K562	blood:
24	chr14:21943958..21946610-chr14:21966325..21968366,2	MCF-7	breast:

No data

Variant related genes	Relation type
METTL3	TF binding region
METTL3	CpG island
ENSG00000092201	chromatin interactions
ENSG00000129472	chromatin interactions
ENSG00000165821	chromatin interactions
ENSG00000165819	chromatin interactions
ENSG00000092203	chromatin interactions
ENSG00000100888	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000260830	chromatin interactions

Extended variants
information (count: 362 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374796848	chr14:21965692-21965693	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs550264500	chr14:21965697-21965698	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570023034	chr14:21965698-21965699	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs10431656	chr14:21965732-21965733	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536048760	chr14:21965754-21965755	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555989682	chr14:21965757-21965758	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552669200	chr14:21965764-21965765	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535315208	chr14:21965775-21965776	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs553838074	chr14:21965876-21965877	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368824548	chr14:21965885-21965886	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576791192	chr14:21965892-21965893	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191609265	chr14:21965914-21965915	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375559291	chr14:21965951-21965952	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs562608374	chr14:21965957-21965958	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576015685	chr14:21965961-21965962	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs71419141	chr14:21965966-21965967	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111603070	chr14:21966008-21966009	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs4982450	chr14:21966009-21966010	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs561540356	chr14:21966029-21966030	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527606896	chr14:21966036-21966037	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs540907983	chr14:21966079-21966080	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs57576078	chr14:21966102-21966103	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs184085221	chr14:21966104-21966105	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533384722	chr14:21966108-21966109	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560991810	chr14:21966160-21966161	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs139565757	chr14:21966202-21966203	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs530869529	chr14:21966214-21966215	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs570142073	chr14:21966256-21966257	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs36040169	chr14:21966299-21966300	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs371381622	chr14:21966301-21966302	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs570338209	chr14:21966314-21966315	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529367261	chr14:21966342-21966343	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs377724885	chr14:21966361-21966362	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs368210531	chr14:21966392-21966393	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs371181847	chr14:21966404-21966405	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs1802004	chr14:21966436-21966437	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs17854735	chr14:21966442-21966443	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs549627481	chr14:21966454-21966455	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs200568556	chr14:21966455-21966456	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs144555583	chr14:21966460-21966461	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs535195781	chr14:21966517-21966518	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs149731858	chr14:21966583-21966584	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs146727711	chr14:21966584-21966585	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs539430422	chr14:21966589-21966590	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs552202307	chr14:21966605-21966606	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs555878204	chr14:21966606-21966607	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs576131685	chr14:21966611-21966612	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs188130510	chr14:21966626-21966627	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs139371969	chr14:21966627-21966628	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs144160065	chr14:21966690-21966691	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ewing''s sarcoma	18628472	CNVD
Rheumatoid arthritis	23223014	CNVD
Ependymoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21946200-21977600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:21946400-21971400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:21947000-21978000	Weak transcription	Fetal Heart	heart
4	chr14:21954600-21967000	Strong transcription	Primary T helper cells fromperipheralblood	blood
5	chr14:21954600-21972600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr14:21954800-21966600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:21954800-21967000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:21954800-21967000	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr14:21954800-21971400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr14:21954800-21972000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr14:21954800-21972000	Strong transcription	Fetal Muscle Trunk	muscle
12	chr14:21954800-21972200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr14:21954800-21972200	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr14:21954800-21977400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:21955000-21967000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr14:21955000-21972000	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr14:21955000-21972400	Strong transcription	Fetal Thymus	thymus
18	chr14:21955200-21966800	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr14:21955200-21972000	Strong transcription	Primary B cells from peripheral blood	blood
20	chr14:21955200-21972200	Strong transcription	Liver	Liver
21	chr14:21955200-21972600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr14:21955400-21966600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr14:21955400-21966600	Strong transcription	Duodenum Smooth Muscle	Duodenum
24	chr14:21955400-21967000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr14:21955400-21967400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:21955400-21971400	Strong transcription	Placenta	Placenta
27	chr14:21955400-21971600	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr14:21955400-21972000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr14:21955400-21972000	Strong transcription	Fetal Intestine Large	intestine
30	chr14:21955400-21972000	Strong transcription	Placenta Amnion	Placenta Amnion
31	chr14:21955400-21972200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr14:21955400-21972200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:21955400-21972200	Strong transcription	Brain Anterior Caudate	brain
34	chr14:21955400-21972600	Strong transcription	Dnd41	blood
35	chr14:21955600-21966200	Strong transcription	Esophagus	oesophagus
36	chr14:21955600-21966400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
37	chr14:21955600-21966400	Strong transcription	Fetal Intestine Small	intestine
38	chr14:21955600-21966600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr14:21955600-21966600	Strong transcription	HepG2	liver
40	chr14:21955600-21967000	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr14:21955600-21967000	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr14:21955600-21967000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr14:21955600-21967000	Strong transcription	NHDF-Ad	bronchial
44	chr14:21955600-21971400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr14:21955600-21971400	Strong transcription	Fetal Muscle Leg	muscle
46	chr14:21955600-21972000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr14:21955600-21972000	Strong transcription	Brain Hippocampus Middle	brain
48	chr14:21955600-21972000	Strong transcription	Duodenum Mucosa	Duodenum
49	chr14:21955600-21972000	Strong transcription	Fetal Lung	lung
50	chr14:21955600-21972000	Strong transcription	Fetal Stomach	stomach

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