Variant report

Variant	nsv869714
Chromosome Location	chr14:21357043-21424185
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	ARID3A	chr14:21423410-21423550	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:21423250-21423720	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
3	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
4	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
5	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
6	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
7	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
8	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
9	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
10	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
11	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
12	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
13	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
14	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
15	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
16	CEBPB	chr14:21423326-21423702	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
17	CEBPB	chr14:21423393-21423620	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
18	CEBPB	chr14:21423483-21423531	A549	lung:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
19	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
20	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
21	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
22	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
23	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
24	CEBPB	chr14:21423391-21423541	Hela-S3	cervix:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
25	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
26	CEBPB	chr14:21423324-21423698	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
27	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
28	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
29	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
30	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
32	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
36	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
38	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
39	CEBPD	chr14:21423329-21423575	HepG2	liver:	n/a	chr14:21423499-21423510
40	CTCF	chr14:21372660-21372910	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr14:21402413-21402575	Medullo	brain:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
42	CTCF	chr14:21402420-21402570	AG09309	skin:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
43	CTCF	chr14:21402308-21402616	K562	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
44	CTCF	chr14:21402400-21402550	HMEC	breast:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
45	CTCF	chr14:21372573-21372869	K562	blood:	n/a	n/a
46	CTCF	chr14:21402404-21402628	HUVEC	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
47	CTCF	chr14:21402400-21402550	HepG2	liver:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
48	CTCF	chr14:21402393-21402642	GM12878	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
49	CTCF	chr14:21402420-21402570	GM12875	blood:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
50	CTCF	chr14:21402360-21402510	NHDF-neo	bronchial:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21423837-21423887	H1-hESC	embryonic stem cell:	embryo
2	chr14:21423837-21423887	H1-hESC	embryonic stem cell:	embryo
3	chr14:21423769-21423819	SAEC	small airway:	n/a
4	chr14:21422205-21422255	MCF10A-Er-Src	breast:	n/a
5	chr14:21359943-21359993	HNPCEpiC	eye:	n/a
6	chr14:21358099-21358149	NHDF-neo	bronchial:	n/a
7	chr14:21422605-21422655	NT2-D1	testis:	n/a
8	chr14:21358233-21358283	GM12891	blood:	n/a
9	chr14:21359737-21359787	SKMC	muscle:	n/a
10	chr14:21423769-21423819	HPAEpiC	pulmonary alveolar:	n/a
11	chr14:21422605-21422655	HMEC	breast:	n/a
12	chr14:21423769-21423819	GM12891	blood:	n/a
13	chr14:21359943-21359993	H1-hESC	embryonic stem cell:	embryo
14	chr14:21359737-21359787	SK-N-SH_RA	brain:	n/a
15	chr14:21386453-21386503	HCPEpiC	choroid plexus:	n/a
16	chr14:21423769-21423819	HRPEpiC	eye:	n/a
17	chr14:21358099-21358149	HCT-116	colon:	n/a
18	chr14:21359295-21359345	NT2-D1	testis:	n/a
19	chr14:21424117-21424167	SK-N-SH	brain:	n/a
20	chr14:21423769-21423819	ECC-1	luminal epithelium:	n/a
21	chr14:21386453-21386503	MCF-7	breast:	n/a
22	chr14:21358233-21358283	BJ	skin:	n/a
23	chr14:21359295-21359345	NH-A	brain:	n/a
24	chr14:21422205-21422255	HEK293	kidney:	embryo
25	chr14:21422965-21423015	NHBE	bronchial:	n/a
26	chr14:21423684-21423734	U87	brain:	n/a
27	chr14:21422965-21423015	SK-N-SH	brain:	n/a
28	chr14:21423769-21423819	PrEC	prostate:	n/a
29	chr14:21423684-21423734	ProgFib	skin:	n/a
30	chr14:21359295-21359345	AG09319	gingival:	n/a
31	chr14:21358233-21358283	HRPEpiC	eye:	n/a
32	chr14:21359295-21359345	HepG2	liver:	n/a
33	chr14:21424117-21424167	HEK293	kidney:	embryo
34	chr14:21422205-21422255	GM12892	blood:	n/a
35	chr14:21423684-21423734	NH-A	brain:	n/a
36	chr14:21386453-21386503	U87	brain:	n/a
37	chr14:21423769-21423819	HRE	kidney:	n/a
38	chr14:21358099-21358149	SK-N-SH_RA	brain:	n/a
39	chr14:21359737-21359787	HPAEpiC	pulmonary alveolar:	n/a
40	chr14:21358233-21358283	SK-N-SH_RA	brain:	n/a
41	chr14:21422605-21422655	MCF10A-Er-Src	breast:	n/a
42	chr14:21422965-21423015	NT2-D1	testis:	n/a
43	chr14:21358099-21358149	NH-A	brain:	n/a
44	chr14:21358099-21358149	SAEC	small airway:	n/a
45	chr14:21359943-21359993	HCF	heart:	n/a
46	chr14:21423837-21423887	U87	brain:	n/a
47	chr14:21359943-21359993	MCF10A-Er-Src	breast:	n/a
48	chr14:21424117-21424167	PrEC	prostate:	n/a
49	chr14:21422605-21422655	HRPEpiC	eye:	n/a
50	chr14:21358099-21358149	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:
2	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
2	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772
3	lnc-RNASE2-1	chr14:21418698-21418708	NONHSAT035618
4	lnc-RNASE2-1	chr14:21419045-21419476	NONHSAT035618
5	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
6	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
7	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
8	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918

Variant related genes	Relation type
ENSG00000258772	TF binding region
ENSG00000136315	TF binding region
RNASE3	TF binding region
ENSG00000258918	TF binding region
RNASE2	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
RNASE3	CpG island
ENSG00000258918	CpG island
RNASE2	CpG island

Extended variants
information (count: 2075 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79406996	chr14:21357105-21357106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs139793518	chr14:21357107-21357108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576292509	chr14:21357125-21357126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs10148067	chr14:21357147-21357148	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs547832922	chr14:21357154-21357155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10133833	chr14:21357219-21357220	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs187017246	chr14:21357227-21357228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552875606	chr14:21357250-21357251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530565353	chr14:21357258-21357259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377562746	chr14:21357259-21357260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537075591	chr14:21357326-21357327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2236283	chr14:21357342-21357343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570761779	chr14:21357366-21357367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573796196	chr14:21357420-21357421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145009124	chr14:21357447-21357448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147552903	chr14:21357459-21357460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140728098	chr14:21357481-21357482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200481106	chr14:21357485-21357486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553228444	chr14:21357489-21357490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544964455	chr14:21357499-21357500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565230272	chr14:21357501-21357502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28563038	chr14:21357503-21357504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568214820	chr14:21357527-21357528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56145810	chr14:21357547-21357548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544231262	chr14:21357570-21357571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557530686	chr14:21357582-21357583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117293018	chr14:21357609-21357610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547121764	chr14:21357626-21357627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115041391	chr14:21357641-21357642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532789075	chr14:21357659-21357660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150102555	chr14:21357665-21357666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114080803	chr14:21357668-21357669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76764740	chr14:21357669-21357670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550617783	chr14:21357682-21357683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117019962	chr14:21357686-21357687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75559351	chr14:21357707-21357708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61980362	chr14:21357708-21357709	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs572948356	chr14:21357718-21357719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538855535	chr14:21357729-21357730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558414093	chr14:21357736-21357737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116652447	chr14:21357744-21357745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371330074	chr14:21357766-21357767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544170292	chr14:21357802-21357803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560947714	chr14:21357804-21357805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574549966	chr14:21357805-21357806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs28532533	chr14:21357845-21357846	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs560665623	chr14:21357847-21357848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1957335	chr14:21357856-21357857	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs546395976	chr14:21357867-21357868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563148497	chr14:21357888-21357889	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:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21354400-21357200	Weak transcription	Thymus	Thymus
2	chr14:21355800-21358200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr14:21356000-21359200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr14:21356000-21362200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr14:21356200-21357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr14:21356800-21359400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr14:21357200-21357400	Enhancers	Thymus	Thymus
8	chr14:21358200-21358600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr14:21358600-21359600	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr14:21359200-21360400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr14:21359400-21359800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr14:21359600-21359800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr14:21359800-21360000	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr14:21360000-21360200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr14:21360200-21360800	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr14:21360400-21362400	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr14:21360800-21361200	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr14:21361200-21362200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr14:21362200-21363200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr14:21362200-21364600	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr14:21362400-21363400	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr14:21363200-21363800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr14:21363400-21364200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr14:21363800-21364600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr14:21364200-21364400	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr14:21364400-21364800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr14:21364600-21365600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr14:21364600-21365600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr14:21364800-21365400	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr14:21365400-21365600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr14:21365600-21372400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr14:21370400-21370600	Enhancers	Gastric	stomach
33	chr14:21371800-21373000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr14:21371800-21375600	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr14:21372400-21372600	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr14:21372400-21372800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr14:21372400-21373000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr14:21372400-21373000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr14:21372400-21373200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr14:21372400-21373200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr14:21372400-21373200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr14:21372400-21373200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr14:21372600-21373000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:21372600-21373000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:21372600-21373000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr14:21372600-21374600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr14:21372600-21374800	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr14:21372800-21373200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr14:21373000-21373400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr14:21373400-21374000	Enhancers	Primary B cells from cord blood	blood

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