Variant report

Variant	esv1008270
Chromosome Location	chr16:48474586-48482323
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:230)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:230 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:48475749-48476306	HepG2	liver:	n/a	n/a
2	ATF1	chr16:48478636-48478798	K562	blood:	n/a	n/a
3	ATF3	chr16:48475700-48476271	A549	lung:	n/a	n/a
4	ATF3	chr16:48475694-48476193	A549	lung:	n/a	n/a
5	BCL3	chr16:48475642-48476236	A549	lung:	n/a	chr16:48475948-48475957
6	BCL3	chr16:48475697-48476191	A549	lung:	n/a	chr16:48475948-48475957
7	BHLHE40	chr16:48481532-48481564	HepG2	liver:	n/a	n/a
8	BHLHE40	chr16:48480444-48480631	K562	blood:	n/a	n/a
9	BHLHE40	chr16:48475724-48476094	HepG2	liver:	n/a	n/a
10	BRCA1	chr16:48478545-48478980	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr16:48475640-48476284	A549	lung:	n/a	n/a
12	CEBPB	chr16:48478495-48479061	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr16:48474904-48474927	K562	blood:	n/a	n/a
14	CEBPB	chr16:48475788-48476104	HepG2	liver:	n/a	n/a
15	CEBPB	chr16:48474812-48475012	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr16:48478576-48479212	Hela-S3	cervix:	n/a	n/a
17	CREB1	chr16:48478488-48478833	A549	lung:	n/a	n/a
18	CREB1	chr16:48478530-48478905	ECC-1	luminal epithelium:	n/a	n/a
19	CREB1	chr16:48478504-48478789	A549	lung:	n/a	n/a
20	CREB1	chr16:48478541-48478911	ECC-1	luminal epithelium:	n/a	n/a
21	CREB1	chr16:48475657-48476022	A549	lung:	n/a	n/a
22	CREB1	chr16:48475764-48475987	A549	lung:	n/a	n/a
23	CREB1	chr16:48476026-48476181	A549	lung:	n/a	n/a
24	CTCF	chr16:48478500-48478650	HCT-116	colon:	n/a	n/a
25	CTCF	chr16:48479040-48479190	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr16:48481840-48481990	HepG2	liver:	n/a	chr16:48481924-48481932
27	CTCF	chr16:48481980-48482130	HepG2	liver:	n/a	n/a
28	CTCF	chr16:48481960-48482110	GM12871	blood:	n/a	n/a
29	EP300	chr16:48478565-48478857	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr16:48475626-48476273	HepG2	liver:	n/a	chr16:48476009-48476019
31	EP300	chr16:48478477-48479386	ECC-1	luminal epithelium:	n/a	n/a
32	EP300	chr16:48478545-48478782	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr16:48481885-48482325	HepG2	liver:	n/a	chr16:48482085-48482095
34	EP300	chr16:48475676-48476298	A549	lung:	n/a	chr16:48476009-48476019
35	EP300	chr16:48478377-48479017	A549	lung:	n/a	n/a
36	EP300	chr16:48478565-48478892	Hela-S3	cervix:	n/a	n/a
37	EP300	chr16:48482026-48482268	HepG2	liver:	n/a	chr16:48482085-48482095
38	EP300	chr16:48475632-48476302	HepG2	liver:	n/a	chr16:48476009-48476019
39	EP300	chr16:48475530-48476266	A549	lung:	n/a	chr16:48476009-48476019 chr16:48475590-48475604
40	FOS	chr16:48478533-48478901	MCF10A-Er-Src	breast:	n/a	chr16:48478714-48478725
41	FOS	chr16:48478589-48478879	HUVEC	blood vessel:	n/a	chr16:48478714-48478725
42	FOS	chr16:48478551-48478886	MCF10A-Er-Src	breast:	n/a	chr16:48478714-48478725
43	FOS	chr16:48478571-48478888	MCF10A-Er-Src	breast:	n/a	chr16:48478714-48478725
44	FOS	chr16:48478487-48478890	MCF10A-Er-Src	breast:	n/a	chr16:48478714-48478725
45	FOSL1	chr16:48478474-48479058	HCT-116	colon:	n/a	n/a
46	FOSL2	chr16:48478520-48478855	A549	lung:	n/a	n/a
47	FOSL2	chr16:48475737-48476078	A549	lung:	n/a	n/a
48	FOSL2	chr16:48478513-48478940	SK-N-SH	brain:	n/a	n/a
49	FOSL2	chr16:48475656-48476285	A549	lung:	n/a	n/a
50	FOSL2	chr16:48475673-48476269	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:48479333-48479383	SK-N-MC	brain:	n/a
2	chr16:48479333-48479383	GM12892	blood:	n/a
3	chr16:48479333-48479383	Jurkat	blood:	n/a
4	chr16:48479333-48479383	NH-A	brain:	n/a
5	chr16:48479333-48479383	K562	blood:	n/a
6	chr16:48479333-48479383	LNCaP	prostate:	n/a
7	chr16:48479333-48479383	HAEpiC	amniotic membrane:	n/a
8	chr16:48479333-48479383	HCM	heart:	n/a
9	chr16:48479333-48479383	Hepatocyte	liver:	n/a
10	chr16:48479333-48479383	HUVEC	blood vessel:	n/a
11	chr16:48479333-48479383	NT2-D1	testis:	n/a
12	chr16:48479333-48479383	SK-N-SH_RA	brain:	n/a
13	chr16:48479333-48479383	HCPEpiC	choroid plexus:	n/a
14	chr16:48479333-48479383	ProgFib	skin:	n/a
15	chr16:48479333-48479383	AG04450	lung:	fetal
16	chr16:48479333-48479383	U87	brain:	n/a
17	chr16:48479333-48479383	MCF-7	breast:	n/a
18	chr16:48479333-48479383	NB4	blood:	n/a
19	chr16:48479333-48479383	HEEpiC	esophagus:	n/a
20	chr16:48479333-48479383	AoSMC	blood vessel:	n/a
21	chr16:48479333-48479383	HMEC	breast:	n/a
22	chr16:48479333-48479383	NHBE	bronchial:	n/a
23	chr16:48479333-48479383	RPTEC	kidney:	n/a
24	chr16:48479333-48479383	HIPEpiC	eye:	n/a
25	chr16:48479333-48479383	HCF	heart:	n/a
26	chr16:48479333-48479383	AG10803	skin:	n/a
27	chr16:48479333-48479383	ovcar-3	ovarian:	n/a
28	chr16:48479333-48479383	HepG2	liver:	n/a
29	chr16:48479333-48479383	Hela-S3	cervix:	n/a
30	chr16:48479333-48479383	Caco-2	colon:	n/a
31	chr16:48479333-48479383	IMR90	lung:	fetal
32	chr16:48479333-48479383	AG09309	skin:	n/a
33	chr16:48479333-48479383	PrEC	prostate:	n/a
34	chr16:48479333-48479383	T-47D	breast:	n/a
35	chr16:48479333-48479383	AG09319	gingival:	n/a
36	chr16:48479333-48479383	GM19239	blood:	n/a
37	chr16:48479333-48479383	PFSK-1	brain:	n/a
38	chr16:48479333-48479383	PANC-1	pancreas:	n/a
39	chr16:48479333-48479383	HL-60	blood:	n/a
40	chr16:48479333-48479383	HNPCEpiC	eye:	n/a
41	chr16:48479333-48479383	ECC-1	luminal epithelium:	n/a
42	chr16:48479333-48479383	GM06990	blood:	n/a
43	chr16:48479333-48479383	HRCEpiC	kidney:	n/a
44	chr16:48479333-48479383	GM12891	blood:	n/a
45	chr16:48479333-48479383	MCF10A-Er-Src	breast:	n/a
46	chr16:48479333-48479383	SK-N-SH	brain:	n/a
47	chr16:48479333-48479383	HCT-116	colon:	n/a
48	chr16:48479333-48479383	SKMC	muscle:	n/a
49	chr16:48479333-48479383	H1-hESC	embryonic stem cell:	embryo
50	chr16:48479333-48479383	HEK293	kidney:	embryo

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:48418147..48420049-chr16:48475413..48478190,2	MCF-7	breast:
2	chr16:48478297..48479194-chr17:26988911..26989673,2	Hela-S3	cervix:
3	chr16:48476815..48479207-chr16:48481453..48484323,3	K562	blood:
4	chr16:48477173..48479098-chr16:48481860..48483849,2	K562	blood:
5	chr16:48478868..48479549-chr21:44816264..44817248,2	Hela-S3	cervix:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-N4BP1-1	chr16:48481815-48481992	ENSG00000261802.1
2	lnc-N4BP1-1	chr16:48482180-48482309	ENSG00000261802.1

No data

Variant related genes	Relation type
SIAH1	TF binding region
ENSG00000261802	TF binding region
SIAH1	CpG island
ENSG00000261802	CpG island
ENSG00000261802	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000196470	chromatin interactions
ENSG00000132581	chromatin interactions

Extended variants
information (count: 295 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7192792	chr16:48474590-48474591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369091556	chr16:48474612-48474613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79053506	chr16:48474618-48474619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564374007	chr16:48474644-48474645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146184435	chr16:48474650-48474651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374467441	chr16:48474658-48474659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558852824	chr16:48474690-48474691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368401625	chr16:48474739-48474740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116815823	chr16:48474791-48474792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7193517	chr16:48474923-48474924	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs7188781	chr16:48474924-48474925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs150769363	chr16:48474967-48474968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75365421	chr16:48474973-48474974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146366706	chr16:48474974-48474975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181768952	chr16:48474979-48474980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537323512	chr16:48474981-48474982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs66497668	chr16:48475003-48475004	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs575973334	chr16:48475008-48475009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138001827	chr16:48475036-48475037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555436471	chr16:48475064-48475065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549754671	chr16:48475082-48475083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185277174	chr16:48475125-48475126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541237186	chr16:48475160-48475161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564239461	chr16:48475161-48475162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578020956	chr16:48475188-48475189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370665749	chr16:48475225-48475226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543726321	chr16:48475226-48475227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563574264	chr16:48475294-48475295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142437731	chr16:48475297-48475298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549063142	chr16:48475298-48475299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568910870	chr16:48475317-48475318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374053291	chr16:48475318-48475319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542203521	chr16:48475322-48475323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559809022	chr16:48475356-48475357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528534246	chr16:48475368-48475369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9923500	chr16:48475391-48475392	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs189003518	chr16:48475398-48475399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537380687	chr16:48475399-48475400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145961297	chr16:48475402-48475403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59871749	chr16:48475423-48475424	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35419764	chr16:48475457-48475458	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371267150	chr16:48475501-48475502	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs117119330	chr16:48475504-48475505	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113687806	chr16:48475523-48475524	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545894916	chr16:48475547-48475548	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374588477	chr16:48475548-48475549	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368170838	chr16:48475559-48475560	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs200898450	chr16:48475561-48475562	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534679048	chr16:48475597-48475598	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375461222	chr16:48475599-48475600	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Disease	22140031	CNVD
Non-syndromic sensorineural hearing loss	22140031	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48466400-48487200	Weak transcription	Right Ventricle	heart
2	chr16:48469200-48478400	Weak transcription	Lung	lung
3	chr16:48470000-48474800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr16:48470200-48475200	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr16:48470200-48475400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr16:48470200-48478800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr16:48472800-48475000	Weak transcription	A549	lung
8	chr16:48472800-48478200	Weak transcription	HMEC	breast
9	chr16:48473200-48478400	Weak transcription	Placenta	Placenta
10	chr16:48475000-48475200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr16:48475000-48475600	Enhancers	A549	lung
12	chr16:48475200-48475400	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr16:48475200-48475600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr16:48475200-48475800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr16:48475200-48478600	Enhancers	HepG2	liver
16	chr16:48475400-48475800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr16:48475600-48476600	Flanking Active TSS	A549	lung
18	chr16:48475600-48478800	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr16:48475800-48476000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr16:48475800-48478600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr16:48475800-48478800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr16:48475800-48480600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr16:48476600-48478600	Enhancers	A549	lung
24	chr16:48476800-48477000	Weak transcription	Colonic Mucosa	Colon
25	chr16:48477000-48477200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr16:48477000-48477200	Enhancers	Colonic Mucosa	Colon
27	chr16:48477200-48478200	Weak transcription	Colonic Mucosa	Colon
28	chr16:48477200-48478400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr16:48478000-48478600	Enhancers	Hela-S3	cervix
30	chr16:48478000-48479400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr16:48478200-48478600	Enhancers	Colonic Mucosa	Colon
32	chr16:48478200-48478600	Enhancers	NH-A	brain
33	chr16:48478200-48478800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr16:48478200-48479000	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr16:48478200-48479400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr16:48478200-48479400	Enhancers	HMEC	breast
37	chr16:48478400-48478800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr16:48478400-48478800	Enhancers	Osteobl	bone
39	chr16:48478400-48479000	Enhancers	Adipose Nuclei	Adipose
40	chr16:48478400-48479200	Enhancers	Stomach Mucosa	stomach
41	chr16:48478400-48479400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr16:48478400-48479400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr16:48478400-48479400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr16:48478400-48479400	Enhancers	HUVEC	blood vessel
45	chr16:48478400-48479400	Enhancers	NHEK	skin
46	chr16:48478400-48480200	Enhancers	Lung	lung
47	chr16:48478400-48480400	Enhancers	Placenta	Placenta
48	chr16:48478400-48480800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr16:48478600-48478800	Bivalent Enhancer	HepG2	liver
50	chr16:48478600-48479000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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