Variant report

Variant	nsv826876
Chromosome Location	chr14:21348259-21412212
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	ATF1	chr14:21349520-21349644	K562	blood:	n/a	n/a
2	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
3	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
5	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
6	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
7	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
8	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
9	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
10	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
11	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
12	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
13	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
14	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
15	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
16	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
17	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
18	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
19	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
20	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
21	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
22	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
24	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
26	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
27	CEBPB	chr14:21387197-21387553	H1-hESC	embryonic stem cell:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
28	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
29	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
30	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
32	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
33	CTCF	chr14:21403520-21403670	HCT-116	colon:	n/a	n/a
34	CTCF	chr14:21402460-21402610	GM12869	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
35	CTCF	chr14:21402440-21402590	HepG2	liver:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
36	CTCF	chr14:21402040-21402190	HCT-116	colon:	n/a	n/a
37	CTCF	chr14:21402393-21402642	GM12878	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
38	CTCF	chr14:21402429-21402581	Pancreas_OC	pancreas:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
39	CTCF	chr14:21402420-21402570	GM12871	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
40	CTCF	chr14:21402380-21402530	HAc	cerebellar:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
41	CTCF	chr14:21386809-21386839	LNCaP	prostate:	n/a	n/a
42	CTCF	chr14:21402423-21402611	Spleen_OC	spleen:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
43	CTCF	chr14:21402380-21402530	HFF-Myc	foreskin:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
44	CTCF	chr14:21402400-21402550	HCPEpiC	choroid plexus:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
45	CTCF	chr14:21402440-21402590	HVMF	connective:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
46	CTCF	chr14:21372521-21372908	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr14:21402343-21402658	H1-hESC	embryonic stem cell:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
48	CTCF	chr14:21402440-21402590	Caco-2	colon:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
49	CTCF	chr14:21402420-21402570	AoAF	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
50	CTCF	chr14:21402460-21402610	HRE	kidney:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21358233-21358283	PANC-1	pancreas:	n/a
2	chr14:21386453-21386503	HEEpiC	esophagus:	n/a
3	chr14:21359737-21359787	HCT-116	colon:	n/a
4	chr14:21359737-21359787	HNPCEpiC	eye:	n/a
5	chr14:21358099-21358149	NHBE	bronchial:	n/a
6	chr14:21359295-21359345	SK-N-SH_RA	brain:	n/a
7	chr14:21359943-21359993	HEK293	kidney:	embryo
8	chr14:21358233-21358283	GM06990	blood:	n/a
9	chr14:21359737-21359787	HRPEpiC	eye:	n/a
10	chr14:21359295-21359345	AG09319	gingival:	n/a
11	chr14:21358099-21358149	Hela-S3	cervix:	n/a
12	chr14:21359295-21359345	HMEC	breast:	n/a
13	chr14:21359737-21359787	HRE	kidney:	n/a
14	chr14:21359737-21359787	RPTEC	kidney:	n/a
15	chr14:21386453-21386503	CMK	blood:	n/a
16	chr14:21359295-21359345	HEEpiC	esophagus:	n/a
17	chr14:21359737-21359787	BJ	skin:	n/a
18	chr14:21358099-21358149	HRPEpiC	eye:	n/a
19	chr14:21386453-21386503	Caco-2	colon:	n/a
20	chr14:21358099-21358149	MCF-7	breast:	n/a
21	chr14:21359295-21359345	AG04449	skin:	fetal
22	chr14:21359295-21359345	NB4	blood:	n/a
23	chr14:21359737-21359787	SK-N-MC	brain:	n/a
24	chr14:21359295-21359345	K562	blood:	n/a
25	chr14:21358233-21358283	NHDF-neo	bronchial:	n/a
26	chr14:21358099-21358149	H1-hESC	embryonic stem cell:	embryo
27	chr14:21358099-21358149	T-47D	breast:	n/a
28	chr14:21386453-21386503	HIPEpiC	eye:	n/a
29	chr14:21358099-21358149	HMEC	breast:	n/a
30	chr14:21358099-21358149	HL-60	blood:	n/a
31	chr14:21359943-21359993	ovcar-3	ovarian:	n/a
32	chr14:21359943-21359993	ECC-1	luminal epithelium:	n/a
33	chr14:21358233-21358283	NB4	blood:	n/a
34	chr14:21358099-21358149	NH-A	brain:	n/a
35	chr14:21359943-21359993	GM12892	blood:	n/a
36	chr14:21359737-21359787	Caco-2	colon:	n/a
37	chr14:21359943-21359993	HepG2	liver:	n/a
38	chr14:21358099-21358149	BE2_C	brain:	n/a
39	chr14:21358233-21358283	CMK	blood:	n/a
40	chr14:21358233-21358283	HRPEpiC	eye:	n/a
41	chr14:21358233-21358283	HMEC	breast:	n/a
42	chr14:21359295-21359345	PrEC	prostate:	n/a
43	chr14:21359943-21359993	T-47D	breast:	n/a
44	chr14:21359943-21359993	U87	brain:	n/a
45	chr14:21359943-21359993	HUVEC	blood vessel:	n/a
46	chr14:21386453-21386503	HL-60	blood:	n/a
47	chr14:21359943-21359993	AG10803	skin:	n/a
48	chr14:21359943-21359993	H1-hESC	embryonic stem cell:	embryo
49	chr14:21386453-21386503	ovcar-3	ovarian:	n/a
50	chr14:21359295-21359345	SAEC	small airway:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918
2	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
3	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
4	lnc-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
5	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
6	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772

Variant related genes	Relation type
ENSG00000258772	TF binding region
ENSG00000136315	TF binding region
ENSG00000258642	TF binding region
RNASE3	TF binding region
ENSG00000258918	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
ENSG00000258642	CpG island
RNASE3	CpG island
ENSG00000258918	CpG island

Extended variants
information (count: 1936 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1936 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560906566	chr14:21348268-21348269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555748805	chr14:21348287-21348288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368354672	chr14:21348292-21348293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535068522	chr14:21348295-21348296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558264168	chr14:21348344-21348345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs578075108	chr14:21348387-21348388	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs543620174	chr14:21348404-21348405	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs11845683	chr14:21348410-21348411	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs189951589	chr14:21348430-21348431	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs368325208	chr14:21348441-21348442	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs372162737	chr14:21348447-21348448	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs542923535	chr14:21348471-21348472	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs180759051	chr14:21348495-21348496	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs144833462	chr14:21348524-21348525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540651916	chr14:21348582-21348583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186145464	chr14:21348643-21348644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530437120	chr14:21348654-21348655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6571504	chr14:21348673-21348674	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs563498554	chr14:21348690-21348691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529144712	chr14:21348692-21348693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142772917	chr14:21348745-21348746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566010099	chr14:21348747-21348748	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548850264	chr14:21348770-21348771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs118172636	chr14:21348795-21348796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551816455	chr14:21348814-21348815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571623378	chr14:21348838-21348839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537555723	chr14:21348843-21348844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557233106	chr14:21348851-21348852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150623448	chr14:21348858-21348859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140033681	chr14:21348873-21348874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537690685	chr14:21348875-21348876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112772911	chr14:21348907-21348908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7154102	chr14:21348944-21348945	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs573233316	chr14:21348950-21348951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540587494	chr14:21348952-21348953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6571505	chr14:21348968-21348969	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs6571506	chr14:21348977-21348978	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191823262	chr14:21349063-21349064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140320940	chr14:21349068-21349069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563288932	chr14:21349083-21349084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529079365	chr14:21349084-21349085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549235845	chr14:21349123-21349124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181922906	chr14:21349129-21349130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186577803	chr14:21349196-21349197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71112531	chr14:21349238-21349239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551441285	chr14:21349281-21349282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377388305	chr14:21349282-21349283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190591573	chr14:21349283-21349284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551050508	chr14:21349319-21349320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144239288	chr14:21349328-21349329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21346600-21350200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:21346800-21348800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr14:21347600-21350200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:21347800-21348600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr14:21348000-21348800	Weak transcription	Primary T cells from cord blood	blood
6	chr14:21348000-21350000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr14:21348200-21349400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr14:21348600-21350000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr14:21348800-21349000	Enhancers	Primary T cells from cord blood	blood
10	chr14:21348800-21349200	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr14:21349000-21349800	Weak transcription	Primary T cells from cord blood	blood
12	chr14:21349200-21350200	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr14:21349400-21350000	Enhancers	Fetal Thymus	thymus
14	chr14:21349400-21350000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr14:21349800-21350200	Enhancers	Primary T cells from cord blood	blood
16	chr14:21350000-21350200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr14:21350000-21354200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr14:21350200-21352800	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr14:21350200-21352800	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr14:21350200-21354000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr14:21350200-21354200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr14:21352800-21353200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr14:21352800-21353400	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr14:21352800-21355600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr14:21353400-21353800	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr14:21353800-21355000	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr14:21354000-21354200	Weak transcription	Thymus	Thymus
28	chr14:21354000-21355000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:21354200-21354400	Enhancers	Thymus	Thymus
30	chr14:21354200-21354800	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr14:21354200-21354800	Enhancers	Primary hematopoietic stem cells	blood
32	chr14:21354200-21355200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:21354400-21357200	Weak transcription	Thymus	Thymus
34	chr14:21354800-21355800	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr14:21355000-21356000	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr14:21355200-21356200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:21355600-21356000	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr14:21355800-21358200	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr14:21356000-21359200	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr14:21356000-21362200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr14:21356200-21356800	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr14:21356200-21357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr14:21356800-21359400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr14:21357200-21357400	Enhancers	Thymus	Thymus
45	chr14:21358200-21358600	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr14:21358600-21359600	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr14:21359200-21360400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr14:21359400-21359800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr14:21359600-21359800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr14:21359800-21360000	Enhancers	Primary neutrophils fromperipheralblood	blood

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