Variant report

Variant	nsv832738
Chromosome Location	chr14:20498622-20644451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:385)
CpG islands
(count:489)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20584982-20585271	K562	blood:	n/a	n/a
2	ARID3A	chr14:20512405-20512844	K562	blood:	n/a	n/a
3	ATF1	chr14:20608626-20608778	K562	blood:	n/a	n/a
4	ATF1	chr14:20584956-20585164	K562	blood:	n/a	n/a
5	ATF1	chr14:20561670-20561913	K562	blood:	n/a	n/a
6	ATF3	chr14:20638032-20638356	K562	blood:	n/a	n/a
7	ATF3	chr14:20584968-20585229	K562	blood:	n/a	n/a
8	ATF3	chr14:20512489-20512787	K562	blood:	n/a	n/a
9	BACH1	chr14:20584638-20585505	K562	blood:	n/a	n/a
10	CBX3	chr14:20632656-20632932	K562	blood:	n/a	n/a
11	CBX3	chr14:20512416-20512761	K562	blood:	n/a	n/a
12	CBX3	chr14:20586942-20587293	K562	blood:	n/a	n/a
13	CBX3	chr14:20584916-20585201	K562	blood:	n/a	n/a
14	CBX3	chr14:20586982-20587337	K562	blood:	n/a	n/a
15	CBX3	chr14:20632642-20632904	K562	blood:	n/a	n/a
16	CCNT2	chr14:20516381-20516636	K562	blood:	n/a	n/a
17	CEBPB	chr14:20522008-20522207	HepG2	liver:	n/a	chr14:20522084-20522095
18	CEBPB	chr14:20578620-20578945	K562	blood:	n/a	n/a
19	CEBPB	chr14:20578612-20578943	IMR90	lung:	n/a	n/a
20	CEBPB	chr14:20618584-20618626	A549	lung:	n/a	n/a
21	CEBPB	chr14:20638948-20639275	HepG2	liver:	n/a	chr14:20639103-20639114
22	CEBPB	chr14:20639049-20639270	IMR90	lung:	n/a	chr14:20639103-20639114
23	CEBPB	chr14:20578626-20578939	A549	lung:	n/a	n/a
24	CEBPB	chr14:20631110-20631224	HepG2	liver:	n/a	chr14:20631171-20631182
25	CEBPB	chr14:20643233-20643506	K562	blood:	n/a	chr14:20643311-20643324
26	CEBPB	chr14:20634808-20635061	HepG2	liver:	n/a	chr14:20634950-20634963 chr14:20634951-20634962 chr14:20634950-20634961 chr14:20634952-20634961
27	CEBPB	chr14:20546411-20546602	K562	blood:	n/a	n/a
28	CEBPB	chr14:20638951-20639274	A549	lung:	n/a	chr14:20639103-20639114
29	CEBPB	chr14:20578635-20578967	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:20584757-20585090	K562	blood:	n/a	n/a
31	CEBPB	chr14:20638926-20639276	K562	blood:	n/a	chr14:20639103-20639114
32	CEBPB	chr14:20524789-20524910	A549	lung:	n/a	n/a
33	CEBPB	chr14:20578686-20578922	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:20622449-20622660	HepG2	liver:	n/a	chr14:20622561-20622572
35	CEBPB	chr14:20522010-20522214	K562	blood:	n/a	chr14:20522084-20522095
36	CHD2	chr14:20580655-20580812	GM12878	blood:	n/a	n/a
37	CTCF	chr14:20556922-20556953	LNCaP	prostate:	n/a	n/a
38	CTCF	chr14:20612180-20612330	GM12871	blood:	n/a	n/a
39	CTCF	chr14:20612203-20612350	GM12892	blood:	n/a	n/a
40	CTCF	chr14:20501199-20501221	ProgFib	skin:	n/a	n/a
41	CTCF	chr14:20601613-20601643	GM20000	blood:	n/a	n/a
42	CTCF	chr14:20643620-20643770	RPTEC	kidney:	n/a	n/a
43	CTCF	chr14:20567745-20567752	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:20612111-20612348	K562	blood:	n/a	n/a
45	CTCF	chr14:20556820-20556970	HEK293	kidney:	n/a	chr14:20556904-20556922
46	CTCF	chr14:20643633-20643708	LNCaP	prostate:	n/a	n/a
47	CTCF	chr14:20612139-20612370	A549	lung:	n/a	n/a
48	CTCF	chr14:20643638-20643702	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:20612220-20612370	HCT-116	colon:	n/a	n/a
50	CTCF	chr14:20612200-20612350	MCF-7	breast:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20611696-20611746	NH-A	brain:	n/a
2	chr14:20611696-20611746	NH-A	brain:	n/a
3	chr14:20611696-20611746	ECC-1	luminal epithelium:	n/a
4	chr14:20584239-20584289	HL-60	blood:	n/a
5	chr14:20528812-20528862	NHBE	bronchial:	n/a
6	chr14:20611779-20611829	PANC-1	pancreas:	n/a
7	chr14:20584239-20584289	BE2_C	brain:	n/a
8	chr14:20612220-20612270	HCF	heart:	n/a
9	chr14:20611696-20611746	AoSMC	blood vessel:	n/a
10	chr14:20585753-20585803	T-47D	breast:	n/a
11	chr14:20586367-20586417	HRPEpiC	eye:	n/a
12	chr14:20611696-20611746	SK-N-SH	brain:	n/a
13	chr14:20528812-20528862	HRE	kidney:	n/a
14	chr14:20584239-20584289	BJ	skin:	n/a
15	chr14:20586367-20586417	CMK	blood:	n/a
16	chr14:20611779-20611829	CMK	blood:	n/a
17	chr14:20584239-20584289	AG04449	skin:	fetal
18	chr14:20586367-20586417	PrEC	prostate:	n/a
19	chr14:20611779-20611829	NH-A	brain:	n/a
20	chr14:20584239-20584289	PANC-1	pancreas:	n/a
21	chr14:20502658-20502708	NH-A	brain:	n/a
22	chr14:20502658-20502708	HEK293	kidney:	embryo
23	chr14:20611779-20611829	NT2-D1	testis:	n/a
24	chr14:20585753-20585803	AG04449	skin:	fetal
25	chr14:20528812-20528862	ovcar-3	ovarian:	n/a
26	chr14:20612220-20612270	SAEC	small airway:	n/a
27	chr14:20612220-20612270	HEK293	kidney:	embryo
28	chr14:20612220-20612270	HepG2	liver:	n/a
29	chr14:20528812-20528862	HUVEC	blood vessel:	n/a
30	chr14:20612220-20612270	HPAEpiC	pulmonary alveolar:	n/a
31	chr14:20586367-20586417	Hela-S3	cervix:	n/a
32	chr14:20586367-20586417	A549	lung:	n/a
33	chr14:20528812-20528862	PANC-1	pancreas:	n/a
34	chr14:20612220-20612270	SK-N-SH	brain:	n/a
35	chr14:20586367-20586417	NB4	blood:	n/a
36	chr14:20528812-20528862	IMR90	lung:	fetal
37	chr14:20611779-20611829	AoSMC	blood vessel:	n/a
38	chr14:20584239-20584289	HPAEpiC	pulmonary alveolar:	n/a
39	chr14:20586367-20586417	HIPEpiC	eye:	n/a
40	chr14:20611779-20611829	GM12892	blood:	n/a
41	chr14:20585753-20585803	GM06990	blood:	n/a
42	chr14:20611696-20611746	HCM	heart:	n/a
43	chr14:20502658-20502708	MCF-7	breast:	n/a
44	chr14:20584239-20584289	HNPCEpiC	eye:	n/a
45	chr14:20612220-20612270	PFSK-1	brain:	n/a
46	chr14:20528812-20528862	BJ	skin:	n/a
47	chr14:20585753-20585803	Hela-S3	cervix:	n/a
48	chr14:20502658-20502708	NB4	blood:	n/a
49	chr14:20612220-20612270	HRE	kidney:	n/a
50	chr14:20611779-20611829	MCF-7	breast:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20623957..20624479-chr3:64655642..64656615,2	MCF-7	breast:
2	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
3	chr14:20530040..20532845-chr14:20547946..20550280,2	K562	blood:
4	chr14:20530040..20532845-chr14:20547946..20550280,2	K562	blood:
5	chr14:20615947..20618319-chr14:20622650..20625486,3	K562	blood:
6	chr14:20615947..20618319-chr14:20622650..20625017,2	K562	blood:
7	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
8	chr14:20518924..20521802-chr14:20525808..20527615,2	K562	blood:
9	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
10	chr14:20642540..20645135-chr14:20796578..20798741,2	K562	blood:
11	chr14:20518924..20521802-chr14:20525808..20527615,2	K562	blood:
12	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
13	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
14	chr14:20582658..20584245-chr14:20584576..20586426,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4N5-1	chr14:20617391-20617904	NONHSAT035552

No data

Variant related genes	Relation type
RNA5SP380	TF binding region
OR4K13	TF binding region
OR4N5	TF binding region
OR4K17	TF binding region
RNA5SP381	TF binding region
OR11G1P	TF binding region
ENSG00000265199	TF binding region
OR4T1P	TF binding region
OR4L1	TF binding region
OR4U1P	TF binding region
ENSG00000259095	TF binding region
PSMB7P1	TF binding region
RNA5SP380	CpG island
OR4K13	CpG island
OR4N5	CpG island
OR4K17	CpG island
RNA5SP381	CpG island
OR11G1P	CpG island
ENSG00000265199	CpG island
OR4T1P	CpG island
OR4L1	CpG island
OR4U1P	CpG island
ENSG00000259095	CpG island
PSMB7P1	CpG island
ENSG00000259074	chromatin interactions
ENSG00000176230	chromatin interactions
ENSG00000100814	chromatin interactions
ENSG00000184394	chromatin interactions

Extended variants
information (count: 1825 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1825 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578144153	chr14:20498623-20498624	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs189346045	chr14:20498645-20498646	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs557099448	chr14:20498688-20498689	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs575555972	chr14:20498710-20498711	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs148198878	chr14:20498722-20498723	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs577134204	chr14:20498730-20498731	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs141169987	chr14:20498761-20498762	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs11621354	chr14:20498839-20498840	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs80334366	chr14:20498843-20498844	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs11627711	chr14:20498855-20498856	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs532373356	chr14:20498887-20498888	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs557986210	chr14:20498927-20498928	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs550815502	chr14:20498959-20498960	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs113837853	chr14:20498973-20498974	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs113414396	chr14:20499001-20499002	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs548490735	chr14:20499007-20499008	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs386775254	chr14:20499037-20499038	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs150739750	chr14:20499038-20499039	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs552282670	chr14:20499041-20499042	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs531164982	chr14:20499070-20499071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs34841696	chr14:20499084-20499085	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs35900465	chr14:20499088-20499089	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs397745415	chr14:20499089-20499090	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs137971445	chr14:20499095-20499096	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs113013864	chr14:20499105-20499106	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs113886548	chr14:20499111-20499112	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs536589262	chr14:20499119-20499120	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs554963762	chr14:20499136-20499137	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs139733738	chr14:20499137-20499138	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs11158354	chr14:20499170-20499171	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs550283101	chr14:20499179-20499180	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs11627640	chr14:20499190-20499191	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536425615	chr14:20499196-20499197	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs144215051	chr14:20499212-20499213	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs544675126	chr14:20499214-20499215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs548390380	chr14:20499224-20499225	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs148712836	chr14:20499246-20499247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs553954593	chr14:20499269-20499270	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs542172885	chr14:20499271-20499272	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs142287136	chr14:20499274-20499275	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs78449376	chr14:20499308-20499309	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs551909475	chr14:20499311-20499312	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs576839997	chr14:20499320-20499321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs570381346	chr14:20499335-20499336	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs188134475	chr14:20499338-20499339	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs374448318	chr14:20499341-20499342	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs74326125	chr14:20499473-20499474	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs569157471	chr14:20499515-20499516	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs536429731	chr14:20499524-20499525	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs2105261	chr14:20500015-20500016	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20496200-20499200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr14:20500000-20500400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr14:20502200-20502400	Enhancers	Pancreas	Pancrea
4	chr14:20502400-20504200	Weak transcription	Pancreas	Pancrea
5	chr14:20512200-20512400	Enhancers	K562	blood
6	chr14:20512400-20512800	Flanking Active TSS	K562	blood
7	chr14:20512800-20513200	Enhancers	K562	blood
8	chr14:20513200-20515800	Weak transcription	K562	blood
9	chr14:20514600-20515000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:20515000-20517000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr14:20515800-20517600	Enhancers	K562	blood
12	chr14:20520400-20521400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr14:20533000-20533400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr14:20542800-20543400	Active TSS	Fetal Heart	heart
15	chr14:20561600-20562000	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr14:20574400-20574600	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr14:20580400-20580800	Enhancers	K562	blood
18	chr14:20580800-20584200	Weak transcription	K562	blood
19	chr14:20584200-20584600	Enhancers	K562	blood
20	chr14:20584600-20585000	Flanking Active TSS	K562	blood
21	chr14:20585000-20585200	Enhancers	K562	blood
22	chr14:20585200-20585400	Flanking Active TSS	K562	blood
23	chr14:20585400-20585600	Enhancers	K562	blood
24	chr14:20585400-20585800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr14:20585600-20585800	ZNF genes & repeats	K562	blood
26	chr14:20585800-20586400	Genic enhancers	K562	blood
27	chr14:20586200-20586600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr14:20586400-20586600	Enhancers	K562	blood
29	chr14:20611200-20612600	Enhancers	K562	blood
30	chr14:20612400-20612800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:20613200-20613400	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr14:20613600-20621000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr14:20622200-20622400	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr14:20623000-20624000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
35	chr14:20630600-20630800	ZNF genes & repeats	Pancreas	Pancrea
36	chr14:20638000-20638800	Enhancers	K562	blood
37	chr14:20638400-20638600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr14:20638400-20638800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr14:20638800-20643000	Weak transcription	K562	blood
40	chr14:20643000-20644000	Enhancers	K562	blood
41	chr14:20643400-20643600	Enhancers	Pancreas	Pancrea
42	chr14:20643400-20643800	Enhancers	Stomach Mucosa	stomach
43	chr14:20643800-20645200	Weak transcription	Pancreas	Pancrea
44	chr14:20644000-20644200	Flanking Active TSS	K562	blood
45	chr14:20644200-20644400	Enhancers	Stomach Mucosa	stomach
46	chr14:20644200-20644600	Enhancers	K562	blood

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