Variant report

Variant	esv1813087
Chromosome Location	chr14:22397143-22427926
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	CEBPB	chr14:22425135-22425473	HepG2	liver:	n/a	chr14:22425302-22425313
2	CEBPB	chr14:22398390-22398663	HepG2	liver:	n/a	chr14:22398526-22398537
3	CEBPB	chr14:22409251-22409393	K562	blood:	n/a	n/a
4	CEBPB	chr14:22425167-22425433	IMR90	lung:	n/a	chr14:22425302-22425313
5	CEBPB	chr14:22411672-22411973	A549	lung:	n/a	chr14:22411805-22411816
6	CEBPB	chr14:22409194-22409417	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:22397017-22397228	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:22411660-22411982	HepG2	liver:	n/a	chr14:22411805-22411816
9	CEBPB	chr14:22398448-22398633	A549	lung:	n/a	chr14:22398526-22398537
10	CEBPB	chr14:22398475-22398574	H1-hESC	embryonic stem cell:	n/a	chr14:22398526-22398537
11	CTCF	chr14:22409140-22409290	NHEK	skin:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
12	CTCF	chr14:22408864-22409624	A549	lung:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
13	CTCF	chr14:22409180-22409330	HUVEC	blood vessel:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
14	CTCF	chr14:22409420-22409570	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr14:22401960-22402110	RPTEC	kidney:	n/a	chr14:22402052-22402070
16	CTCF	chr14:22401820-22402195	HepG2	liver:	n/a	chr14:22402052-22402070
17	CTCF	chr14:22409200-22409350	HPF	lung:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
18	CTCF	chr14:22409180-22409330	GM12868	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
19	CTCF	chr14:22409212-22409337	GM13976	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
20	CTCF	chr14:22409223-22409313	GM10248	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
21	CTCF	chr14:22409180-22409330	Caco-2	colon:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
22	CTCF	chr14:22409140-22409290	NB4	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
23	CTCF	chr14:22402001-22402150	Kidney_OC	kidney:	n/a	chr14:22402052-22402070
24	CTCF	chr14:22409200-22409350	GM12864	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
25	CTCF	chr14:22409180-22409330	HEEpiC	esophagus:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
26	CTCF	chr14:22409180-22409331	MCF-7	breast:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
27	CTCF	chr14:22401949-22402162	LNCaP	prostate:	n/a	chr14:22402052-22402070
28	CTCF	chr14:22402000-22402150	GM12870	blood:	n/a	chr14:22402052-22402070
29	CTCF	chr14:22409159-22409346	NHEK	skin:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
30	CTCF	chr14:22401940-22402090	GM12868	blood:	n/a	chr14:22402052-22402070
31	CTCF	chr14:22409180-22409330	HVMF	connective:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
32	CTCF	chr14:22409220-22409370	GM12872	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
33	CTCF	chr14:22409169-22409315	GM19240	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
34	CTCF	chr14:22409560-22409710	MCF-7	breast:	n/a	n/a
35	CTCF	chr14:22409240-22409390	HCM	heart:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
36	CTCF	chr14:22409191-22409350	GM10266	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
37	CTCF	chr14:22401980-22402130	HAc	cerebellar:	n/a	chr14:22402052-22402070
38	CTCF	chr14:22401940-22402090	GM12865	blood:	n/a	chr14:22402052-22402070
39	CTCF	chr14:22409180-22409330	AG04449	skin:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
40	CTCF	chr14:22409180-22409330	HBMEC	blood vessel:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
41	CTCF	chr14:22409220-22409370	HRE	kidney:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
42	CTCF	chr14:22402041-22402080	MCF-7	breast:	n/a	chr14:22402052-22402070
43	CTCF	chr14:22408780-22408930	HepG2	liver:	n/a	n/a
44	CTCF	chr14:22409200-22409350	GM06990	blood:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
45	CTCF	chr14:22408740-22408890	GM12878	blood:	n/a	n/a
46	CTCF	chr14:22401960-22402110	HCM	heart:	n/a	chr14:22402052-22402070
47	CTCF	chr14:22409200-22409350	NHEK	skin:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
48	CTCF	chr14:22401980-22402130	HPAF	blood vessel:	n/a	chr14:22402052-22402070
49	CTCF	chr14:22409162-22409319	MCF-7	breast:	n/a	chr14:22409256-22409265 chr14:22409253-22409271
50	CTCF	chr14:22409032-22409380	A549	lung:	n/a	chr14:22409256-22409265 chr14:22409253-22409271

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22408982-22409032	BE2_C	brain:	n/a
2	chr14:22408982-22409032	H1-hESC	embryonic stem cell:	embryo
3	chr14:22408982-22409032	MCF-7	breast:	n/a
4	chr14:22408982-22409032	HCT-116	colon:	n/a
5	chr14:22408982-22409032	NT2-D1	testis:	n/a
6	chr14:22408982-22409032	HepG2	liver:	n/a
7	chr14:22408982-22409032	NHDF-neo	bronchial:	n/a
8	chr14:22408982-22409032	HMEC	breast:	n/a
9	chr14:22408982-22409032	HAEpiC	amniotic membrane:	n/a
10	chr14:22408982-22409032	A549	lung:	n/a
11	chr14:22408982-22409032	AG09319	gingival:	n/a
12	chr14:22408982-22409032	ECC-1	luminal epithelium:	n/a
13	chr14:22408982-22409032	GM19239	blood:	n/a
14	chr14:22408982-22409032	HUVEC	blood vessel:	n/a
15	chr14:22408982-22409032	NB4	blood:	n/a
16	chr14:22408982-22409032	CMK	blood:	n/a
17	chr14:22408982-22409032	PANC-1	pancreas:	n/a
18	chr14:22408982-22409032	HEK293	kidney:	embryo
19	chr14:22408982-22409032	NH-A	brain:	n/a
20	chr14:22408982-22409032	PFSK-1	brain:	n/a
21	chr14:22408982-22409032	Hela-S3	cervix:	n/a
22	chr14:22408982-22409032	BJ	skin:	n/a
23	chr14:22408982-22409032	HCPEpiC	choroid plexus:	n/a
24	chr14:22408982-22409032	K562	blood:	n/a
25	chr14:22408982-22409032	LNCaP	prostate:	n/a
26	chr14:22408982-22409032	GM12892	blood:	n/a
27	chr14:22408982-22409032	HRCEpiC	kidney:	n/a
28	chr14:22408982-22409032	U87	brain:	n/a
29	chr14:22408982-22409032	AG04450	lung:	fetal
30	chr14:22408982-22409032	ovcar-3	ovarian:	n/a
31	chr14:22408982-22409032	HRE	kidney:	n/a
32	chr14:22408982-22409032	HEEpiC	esophagus:	n/a
33	chr14:22408982-22409032	SAEC	small airway:	n/a
34	chr14:22408982-22409032	HCM	heart:	n/a
35	chr14:22408982-22409032	T-47D	breast:	n/a
36	chr14:22408982-22409032	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:22408982-22409032	IMR90	lung:	fetal
38	chr14:22408982-22409032	SKMC	muscle:	n/a
39	chr14:22408982-22409032	AG04449	skin:	fetal
40	chr14:22408982-22409032	HCF	heart:	n/a
41	chr14:22408982-22409032	AG10803	skin:	n/a
42	chr14:22408982-22409032	GM12878	blood:	n/a
43	chr14:22408982-22409032	Jurkat	blood:	n/a
44	chr14:22408982-22409032	HRPEpiC	eye:	n/a
45	chr14:22408982-22409032	AG09309	skin:	n/a
46	chr14:22408982-22409032	RPTEC	kidney:	n/a
47	chr14:22408982-22409032	SK-N-SH_RA	brain:	n/a
48	chr14:22408982-22409032	Caco-2	colon:	n/a
49	chr14:22408982-22409032	MCF10A-Er-Src	breast:	n/a
50	chr14:22408982-22409032	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:88513529..88515426-chr14:22404451..22405951,2	K562	blood:
2	chr14:22381710..22382649-chr14:22401797..22402492,3	MCF-7	breast:
3	chr14:22336451..22337308-chr14:22401460..22402246,2	MCF-7	breast:
4	chr14:22388102..22388976-chr14:22401807..22402500,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4E2-5	chr14:22418629-22418877	NONHSAT035722

Variant related genes	Relation type
TRAV9-2	TF binding region
TRAV15	TF binding region
TRAV9-2	CpG island
TRAV15	CpG island
ENSG00000211788	chromatin interactions

Extended variants
information (count: 904 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:904 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2204943	chr14:22397143-22397144	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74035435	chr14:22397230-22397231	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs140089427	chr14:22397256-22397257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569481909	chr14:22397272-22397273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577948145	chr14:22397274-22397275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537116041	chr14:22397291-22397292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10144270	chr14:22397342-22397343	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs551237302	chr14:22397454-22397455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567257283	chr14:22397468-22397469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145596501	chr14:22397548-22397549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149754555	chr14:22397584-22397585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371848182	chr14:22397586-22397587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199678056	chr14:22397587-22397588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76783005	chr14:22397608-22397609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573134032	chr14:22397644-22397645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544987166	chr14:22397682-22397683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181997517	chr14:22397696-22397697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201863528	chr14:22397709-22397710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs202158406	chr14:22397710-22397711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs58437558	chr14:22397712-22397713	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs561077624	chr14:22397737-22397738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530012441	chr14:22397813-22397814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548759953	chr14:22397814-22397815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs55950103	chr14:22397842-22397843	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs560613295	chr14:22397850-22397851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532799438	chr14:22397856-22397857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537910798	chr14:22397857-22397858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs55853703	chr14:22397860-22397861	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs57974084	chr14:22397865-22397866	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs74692181	chr14:22397881-22397882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550675172	chr14:22397905-22397906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145702974	chr14:22397921-22397922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535864141	chr14:22397988-22397989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552895756	chr14:22397997-22397998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146589403	chr14:22398011-22398012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538894513	chr14:22398013-22398014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544104491	chr14:22398015-22398016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556239248	chr14:22398026-22398027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187597877	chr14:22398046-22398047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141297306	chr14:22398066-22398067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544028882	chr14:22398086-22398087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554639720	chr14:22398094-22398095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574631825	chr14:22398100-22398101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540379130	chr14:22398189-22398190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143146812	chr14:22398214-22398215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148243059	chr14:22398232-22398233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546461443	chr14:22398268-22398269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563203389	chr14:22398290-22398291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112470921	chr14:22398322-22398323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548842212	chr14:22398340-22398341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Barrett''s syndrome	19417022	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22393000-22399800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr14:22394200-22397200	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr14:22394200-22399600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr14:22394200-22399600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr14:22394400-22399400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:22394400-22399600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr14:22395000-22397200	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr14:22396800-22397600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr14:22396800-22398200	Enhancers	Primary T cells from cord blood	blood
10	chr14:22397000-22397200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:22397000-22397200	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr14:22397000-22397400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr14:22397200-22397400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr14:22397200-22397600	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr14:22397200-22397600	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr14:22397200-22398400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr14:22397400-22398200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr14:22397400-22409400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr14:22398200-22399000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr14:22399400-22399600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr14:22399600-22400000	Flanking Active TSS	Primary hematopoietic stem cells	blood
22	chr14:22399600-22400000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr14:22399600-22400200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:22399600-22400400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr14:22399800-22400000	Flanking Active TSS	Fetal Lung	lung
26	chr14:22399800-22400000	Enhancers	HUVEC	blood vessel
27	chr14:22399800-22400200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr14:22400000-22400400	Enhancers	Primary hematopoietic stem cells	blood
29	chr14:22400000-22400600	Enhancers	Fetal Lung	lung
30	chr14:22400000-22407600	Weak transcription	HUVEC	blood vessel
31	chr14:22400200-22400600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr14:22400400-22401600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:22400600-22405400	Weak transcription	Fetal Lung	lung
34	chr14:22401800-22402000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr14:22405400-22408800	Enhancers	Fetal Lung	lung
36	chr14:22407600-22409600	Enhancers	HUVEC	blood vessel
37	chr14:22408400-22409600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr14:22408600-22409400	Enhancers	Fetal Thymus	thymus
39	chr14:22408800-22409000	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr14:22408800-22409200	Enhancers	Primary T cells from cord blood	blood
41	chr14:22408800-22409600	Enhancers	Thymus	Thymus
42	chr14:22409000-22409400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr14:22409000-22409600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:22409000-22409600	Active TSS	Primary T killer memory cells from peripheral blood	blood
45	chr14:22409000-22409800	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr14:22409200-22409400	Enhancers	Primary T cells fromperipheralblood	blood
47	chr14:22409200-22409400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr14:22409200-22409400	Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr14:22409200-22409800	Flanking Active TSS	Primary T cells from cord blood	blood
50	chr14:22409200-22409800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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