Variant report

Variant	nsv1036728
Chromosome Location	chr14:21338459-21409969
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	BCLAF1	chr14:21341818-21342245	GM12878	blood:	n/a	chr14:21341956-21341969
3	BCLAF1	chr14:21341829-21342279	GM12878	blood:	n/a	chr14:21341956-21341969
4	BHLHE40	chr14:21341894-21342031	K562	blood:	n/a	chr14:21341954-21341970
5	CBX3	chr14:21341821-21342185	K562	blood:	n/a	n/a
6	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
7	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
8	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
10	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
11	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
12	CEBPB	chr14:21359339-21359538	K562	blood:	n/a	chr14:21359447-21359460
13	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
14	CEBPB	chr14:21341896-21342213	MCF-7	breast:	n/a	n/a
15	CEBPB	chr14:21341854-21342226	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr14:21341881-21342104	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:21344519-21344558	HepG2	liver:	n/a	chr14:21344532-21344543
20	CEBPB	chr14:21341879-21342172	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:21341852-21342195	K562	blood:	n/a	n/a
22	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
23	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
24	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
25	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
26	CEBPB	chr14:21390780-21390974	K562	blood:	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	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
29	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
31	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
32	CEBPB	chr14:21341851-21342133	K562	blood:	n/a	n/a
33	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
34	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
35	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
36	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
37	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
38	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
39	CEBPB	chr14:21341785-21342305	A549	lung:	n/a	n/a
40	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
41	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
42	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
43	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
44	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
45	CREB1	chr14:21341864-21342173	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr14:21341735-21342321	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr14:21341376-21342369	A549	lung:	n/a	chr14:21341957-21341973 chr14:21341958-21341971 chr14:21341956-21341974 chr14:21342181-21342194
48	CTCF	chr14:21402460-21402610	HBMEC	blood vessel:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
49	CTCF	chr14:21402320-21402470	HAc	cerebellar:	n/a	n/a
50	CTCF	chr14:21342438-21342445	Spleen_OC	spleen:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21358099-21358149	GM12878	blood:	n/a
2	chr14:21341871-21341921	HUVEC	blood vessel:	n/a
3	chr14:21358233-21358283	AG04450	lung:	fetal
4	chr14:21386453-21386503	HCF	heart:	n/a
5	chr14:21358099-21358149	NHDF-neo	bronchial:	n/a
6	chr14:21386453-21386503	NHDF-neo	bronchial:	n/a
7	chr14:21359943-21359993	PANC-1	pancreas:	n/a
8	chr14:21341871-21341921	HEK293	kidney:	embryo
9	chr14:21341871-21341921	GM12892	blood:	n/a
10	chr14:21342066-21342116	AG09309	skin:	n/a
11	chr14:21341871-21341921	SAEC	small airway:	n/a
12	chr14:21386453-21386503	HEK293	kidney:	embryo
13	chr14:21342066-21342116	HAEpiC	amniotic membrane:	n/a
14	chr14:21342066-21342116	ProgFib	skin:	n/a
15	chr14:21359295-21359345	AG09319	gingival:	n/a
16	chr14:21359295-21359345	AoSMC	blood vessel:	n/a
17	chr14:21341871-21341921	HIPEpiC	eye:	n/a
18	chr14:21358099-21358149	HL-60	blood:	n/a
19	chr14:21359295-21359345	HIPEpiC	eye:	n/a
20	chr14:21358233-21358283	MCF-7	breast:	n/a
21	chr14:21342066-21342116	HCPEpiC	choroid plexus:	n/a
22	chr14:21341871-21341921	BJ	skin:	n/a
23	chr14:21358233-21358283	HCPEpiC	choroid plexus:	n/a
24	chr14:21359943-21359993	GM12878	blood:	n/a
25	chr14:21358233-21358283	K562	blood:	n/a
26	chr14:21342066-21342116	HRCEpiC	kidney:	n/a
27	chr14:21358099-21358149	HIPEpiC	eye:	n/a
28	chr14:21359295-21359345	SK-N-SH_RA	brain:	n/a
29	chr14:21359737-21359787	H1-hESC	embryonic stem cell:	embryo
30	chr14:21359737-21359787	NT2-D1	testis:	n/a
31	chr14:21358099-21358149	SKMC	muscle:	n/a
32	chr14:21359737-21359787	AG09309	skin:	n/a
33	chr14:21359295-21359345	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:21359295-21359345	ovcar-3	ovarian:	n/a
35	chr14:21359737-21359787	GM12891	blood:	n/a
36	chr14:21359737-21359787	AG09319	gingival:	n/a
37	chr14:21341871-21341921	U87	brain:	n/a
38	chr14:21342066-21342116	HNPCEpiC	eye:	n/a
39	chr14:21386453-21386503	NH-A	brain:	n/a
40	chr14:21359737-21359787	U87	brain:	n/a
41	chr14:21342066-21342116	RPTEC	kidney:	n/a
42	chr14:21359295-21359345	HCM	heart:	n/a
43	chr14:21359295-21359345	HEK293	kidney:	embryo
44	chr14:21359737-21359787	HRCEpiC	kidney:	n/a
45	chr14:21359295-21359345	HL-60	blood:	n/a
46	chr14:21359943-21359993	AG10803	skin:	n/a
47	chr14:21358099-21358149	T-47D	breast:	n/a
48	chr14:21341871-21341921	GM12891	blood:	n/a
49	chr14:21359295-21359345	NH-A	brain:	n/a
50	chr14:21359943-21359993	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:21339048..21339766-chr3:63998651..63999205,2	MCF-7	breast:
2	chr14:21341929..21342586-chr14:21439203..21440051,2	K562	blood:
3	chr14:21345187..21348103-chr14:21455224..21457829,2	K562	blood:
4	chr14:21325580..21326139-chr14:21341851..21342353,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASE1-1	chr14:21338438-21338615	ENSG00000259130
2	lnc-RNASE1-1	chr14:21341350-21341529	ENSG00000259130
3	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
4	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
5	lnc-RNASE1-1	chr14:21341079-21342995	XLOC_010966
6	lnc-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
7	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918
8	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772
9	lnc-RNASE1-1	chr14:21340531-21340720	ENSG00000259130
10	lnc-RNASE1-1	chr14:21341718-21341751	ENSG00000259130
11	lnc-RNASE1-1	chr14:21343696-21343904	XLOC_010966
12	lnc-RNASE1-1	chr14:21342464-21342995	ENSG00000258642.1
13	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
14	lnc-RNASE1-1	chr14:21343696-21343927	ENSG00000258642.1
15	lnc-RNASE1-1	chr14:21338437-21338615	ENSG00000259130

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
ENSG00000259130	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
ENSG00000258642	CpG island
RNASE3	CpG island
ENSG00000258918	CpG island
ENSG00000259130	CpG island
ENSG00000163636	chromatin interactions

Extended variants
information (count: 2219 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2219 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11629400	chr14:21338459-21338460	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs149510702	chr14:21338490-21338491	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs183871998	chr14:21338502-21338503	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs376666186	chr14:21338557-21338558	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs146017288	chr14:21338638-21338639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73571885	chr14:21338644-21338645	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs546873404	chr14:21338645-21338646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560231845	chr14:21338659-21338660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7140232	chr14:21338666-21338667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552187907	chr14:21338669-21338670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17097725	chr14:21338687-21338688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73571890	chr14:21338738-21338739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs115098147	chr14:21338739-21338740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568649333	chr14:21338819-21338820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs17097726	chr14:21338824-21338825	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs556484866	chr14:21338837-21338838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189320843	chr14:21338844-21338845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374668195	chr14:21338864-21338865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs60870186	chr14:21338907-21338908	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs538624753	chr14:21338931-21338932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138779986	chr14:21338959-21338960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545616228	chr14:21338966-21338967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182153010	chr14:21339179-21339180	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560870466	chr14:21339209-21339210	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs34224368	chr14:21339216-21339217	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs76261576	chr14:21339219-21339220	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540091742	chr14:21339237-21339238	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs186773268	chr14:21339261-21339262	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs7147480	chr14:21339263-21339264	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs545762431	chr14:21339298-21339299	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562558103	chr14:21339304-21339305	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531654502	chr14:21339306-21339307	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs539914086	chr14:21339343-21339344	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs189966166	chr14:21339398-21339399	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568508093	chr14:21339415-21339416	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs561676895	chr14:21339416-21339417	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs527877463	chr14:21339424-21339425	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs547712551	chr14:21339443-21339444	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs117548386	chr14:21339562-21339563	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550592933	chr14:21339587-21339588	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs540160646	chr14:21339595-21339596	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558556129	chr14:21339656-21339657	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569216619	chr14:21339699-21339700	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77406793	chr14:21339702-21339703	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537489512	chr14:21339719-21339720	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554636495	chr14:21339751-21339752	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574479976	chr14:21339837-21339838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540399407	chr14:21339843-21339844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182129018	chr14:21339853-21339854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78893941	chr14:21339855-21339856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21335600-21338800	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr14:21337200-21341600	Weak transcription	Brain Substantia Nigra	brain
3	chr14:21337600-21341600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:21338800-21341600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr14:21339200-21340200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr14:21340200-21341200	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr14:21341200-21341400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:21341200-21341400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr14:21341200-21341600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
10	chr14:21341200-21342200	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr14:21341200-21342200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr14:21341200-21342200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr14:21341200-21342600	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr14:21341200-21342600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:21341200-21343200	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr14:21341400-21341600	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr14:21341400-21341600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr14:21341400-21341600	Enhancers	Brain Cingulate Gyrus	brain
19	chr14:21341400-21341600	Enhancers	Dnd41	blood
20	chr14:21341400-21341800	Enhancers	Primary T cells from cord blood	blood
21	chr14:21341400-21342200	Active TSS	H1 Cell Line	embryonic stem cell
22	chr14:21341400-21342200	Enhancers	Primary B cells from peripheral blood	blood
23	chr14:21341400-21342200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr14:21341400-21342200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr14:21341400-21342200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr14:21341400-21342400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr14:21341400-21342400	Enhancers	Primary hematopoietic stem cells	blood
28	chr14:21341400-21342400	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr14:21341400-21342400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr14:21341400-21342400	Enhancers	Brain Anterior Caudate	brain
31	chr14:21341400-21342600	Enhancers	Primary B cells from cord blood	blood
32	chr14:21341400-21342600	Enhancers	Spleen	Spleen
33	chr14:21341400-21342600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr14:21341600-21341800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr14:21341600-21341800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr14:21341600-21341800	Flanking Active TSS	Brain Cingulate Gyrus	brain
37	chr14:21341600-21342000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr14:21341600-21342000	Flanking Active TSS	Brain Substantia Nigra	brain
39	chr14:21341600-21342000	Enhancers	Colon Smooth Muscle	Colon
40	chr14:21341600-21342000	Active TSS	GM12878-XiMat	blood
41	chr14:21341600-21342000	Enhancers	HUVEC	blood vessel
42	chr14:21341600-21342200	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr14:21341600-21342200	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr14:21341600-21342200	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr14:21341600-21342200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr14:21341600-21342200	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr14:21341600-21342200	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr14:21341600-21342200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr14:21341600-21342200	Enhancers	Duodenum Mucosa	Duodenum
50	chr14:21341600-21342200	Active TSS	Duodenum Smooth Muscle	Duodenum

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