Variant report

Variant	nsv1045746
Chromosome Location	chr14:40759826-40852546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:239)
CpG islands
(count:244)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:239 , 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	BACH1	chr14:40787269-40787733	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr14:40808595-40808625	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr14:40781497-40781964	HCT-116	colon:	n/a	n/a
4	CEBPB	chr14:40844308-40844652	HepG2	liver:	n/a	n/a
5	CEBPB	chr14:40844332-40844672	IMR90	lung:	n/a	n/a
6	CEBPB	chr14:40777488-40777823	IMR90	lung:	n/a	chr14:40777637-40777648
7	CEBPB	chr14:40817387-40817417	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr14:40781562-40781987	HCT-116	colon:	n/a	n/a
9	CEBPB	chr14:40840922-40841392	HepG2	liver:	n/a	chr14:40841265-40841278 chr14:40841265-40841276 chr14:40841267-40841276
10	CEBPB	chr14:40777455-40777816	HepG2	liver:	n/a	chr14:40777637-40777648
11	CEBPB	chr14:40844357-40844564	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:40777458-40777834	MCF-7	breast:	n/a	chr14:40777637-40777648
13	CEBPB	chr14:40840907-40841139	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr14:40777468-40777787	A549	lung:	n/a	chr14:40777637-40777648
15	CEBPB	chr14:40792398-40792568	HepG2	liver:	n/a	chr14:40792452-40792463 chr14:40792450-40792461
16	CEBPB	chr14:40786957-40787099	HepG2	liver:	n/a	chr14:40787041-40787052
17	CEBPB	chr14:40787701-40787742	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr14:40844299-40844655	A549	lung:	n/a	n/a
19	CEBPB	chr14:40781436-40782040	HCT-116	colon:	n/a	n/a
20	CEBPB	chr14:40777495-40777808	H1-hESC	embryonic stem cell:	n/a	chr14:40777637-40777648
21	CEBPB	chr14:40766084-40766366	HepG2	liver:	n/a	chr14:40766236-40766247 chr14:40766236-40766249
22	CHD1	chr14:40817059-40817259	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr14:40766380-40766530	HepG2	liver:	n/a	n/a
24	CTCF	chr14:40777120-40777270	HepG2	liver:	n/a	n/a
25	CTCF	chr14:40790789-40790857	GM20000	blood:	n/a	n/a
26	CTCF	chr14:40836292-40836352	GM13976	blood:	n/a	n/a
27	CTCF	chr14:40760961-40761141	GM20000	blood:	n/a	n/a
28	CTCF	chr14:40841280-40841430	HPF	lung:	n/a	n/a
29	CTCF	chr14:40795800-40795950	HepG2	liver:	n/a	n/a
30	CTCF	chr14:40817048-40817149	LNCaP	prostate:	n/a	chr14:40817131-40817139
31	CTCF	chr14:40761025-40761077	GM13976	blood:	n/a	n/a
32	CTCF	chr14:40761034-40761072	GM13977	blood:	n/a	n/a
33	CTCF	chr14:40761037-40761076	GM10248	blood:	n/a	n/a
34	CTCF	chr14:40802774-40802798	MCF-7	breast:	n/a	n/a
35	CTCF	chr14:40762880-40763030	HEK293	kidney:	n/a	n/a
36	CTCF	chr14:40761007-40761077	LNCaP	prostate:	n/a	n/a
37	CTCF	chr14:40761036-40761112	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr14:40760338-40760366	GM13977	blood:	n/a	n/a
39	CTCF	chr14:40817033-40817108	LNCaP	prostate:	n/a	n/a
40	CTCF	chr14:40762820-40762970	HepG2	liver:	n/a	n/a
41	CTCF	chr14:40795933-40796005	H1-hESC	embryonic stem cell:	n/a	n/a
42	ELF1	chr14:40834427-40835016	MCF-7	breast:	n/a	chr14:40834998-40835009
43	EP300	chr14:40837426-40838012	T-47D	breast:	n/a	chr14:40837896-40837910 chr14:40837821-40837831 chr14:40837471-40837485 chr14:40837991-40838000 chr14:40837465-40837479 chr14:40837726-40837736
44	EP300	chr14:40834404-40834981	MCF-7	breast:	n/a	chr14:40834946-40834960 chr14:40834908-40834917
45	EP300	chr14:40837572-40837846	T-47D	breast:	n/a	chr14:40837821-40837831 chr14:40837726-40837736
46	EP300	chr14:40837523-40838000	MCF-7	breast:	n/a	chr14:40837896-40837910 chr14:40837821-40837831 chr14:40837991-40838000 chr14:40837726-40837736
47	FOS	chr14:40840281-40840506	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr14:40840310-40840509	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr14:40767358-40767419	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr14:40787038-40787238	MCF10A-Er-Src	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:40817565-40817615	SAEC	small airway:	n/a
2	chr14:40817444-40817494	HepG2	liver:	n/a
3	chr14:40809000-40809050	Caco-2	colon:	n/a
4	chr14:40809000-40809050	ProgFib	skin:	n/a
5	chr14:40817444-40817494	IMR90	lung:	fetal
6	chr14:40809000-40809050	AG10803	skin:	n/a
7	chr14:40817444-40817494	CMK	blood:	n/a
8	chr14:40809000-40809050	HepG2	liver:	n/a
9	chr14:40832309-40832359	MCF10A-Er-Src	breast:	n/a
10	chr14:40809000-40809050	IMR90	lung:	fetal
11	chr14:40817444-40817494	HNPCEpiC	eye:	n/a
12	chr14:40817444-40817494	HCT-116	colon:	n/a
13	chr14:40817565-40817615	Hela-S3	cervix:	n/a
14	chr14:40817565-40817615	K562	blood:	n/a
15	chr14:40817565-40817615	ovcar-3	ovarian:	n/a
16	chr14:40817565-40817615	PANC-1	pancreas:	n/a
17	chr14:40817565-40817615	HL-60	blood:	n/a
18	chr14:40817444-40817494	RPTEC	kidney:	n/a
19	chr14:40809000-40809050	HEK293	kidney:	embryo
20	chr14:40809000-40809050	SKMC	muscle:	n/a
21	chr14:40817565-40817615	BJ	skin:	n/a
22	chr14:40809000-40809050	NH-A	brain:	n/a
23	chr14:40817444-40817494	MCF10A-Er-Src	breast:	n/a
24	chr14:40832309-40832359	NT2-D1	testis:	n/a
25	chr14:40809000-40809050	A549	lung:	n/a
26	chr14:40832309-40832359	NHBE	bronchial:	n/a
27	chr14:40832309-40832359	GM12892	blood:	n/a
28	chr14:40817565-40817615	HEEpiC	esophagus:	n/a
29	chr14:40817444-40817494	NB4	blood:	n/a
30	chr14:40817565-40817615	HUVEC	blood vessel:	n/a
31	chr14:40817565-40817615	HRPEpiC	eye:	n/a
32	chr14:40817565-40817615	HMEC	breast:	n/a
33	chr14:40809000-40809050	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:40817444-40817494	PFSK-1	brain:	n/a
35	chr14:40832309-40832359	RPTEC	kidney:	n/a
36	chr14:40817565-40817615	HEK293	kidney:	embryo
37	chr14:40809000-40809050	GM12878	blood:	n/a
38	chr14:40817444-40817494	ProgFib	skin:	n/a
39	chr14:40832309-40832359	BJ	skin:	n/a
40	chr14:40817565-40817615	HCM	heart:	n/a
41	chr14:40809000-40809050	LNCaP	prostate:	n/a
42	chr14:40809000-40809050	NB4	blood:	n/a
43	chr14:40817444-40817494	AG09319	gingival:	n/a
44	chr14:40817444-40817494	HPAEpiC	pulmonary alveolar:	n/a
45	chr14:40817444-40817494	H1-hESC	embryonic stem cell:	embryo
46	chr14:40817565-40817615	ProgFib	skin:	n/a
47	chr14:40817444-40817494	NH-A	brain:	n/a
48	chr14:40809000-40809050	HAEpiC	amniotic membrane:	n/a
49	chr14:40809000-40809050	BE2_C	brain:	n/a
50	chr14:40809000-40809050	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:40762742..40765094-chr14:40766225..40768679,2	K562	blood:
2	chr14:40762742..40765094-chr14:40766225..40768679,2	K562	blood:
3	chr14:40852272..40855989-chr14:40856721..40860430,4	MCF-7	breast:
4	chr14:40839183..40841621-chr14:40841712..40843758,2	MCF-7	breast:
5	chr14:40839183..40841621-chr14:40841712..40843758,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000258418	TF binding region
ENSG00000258480	TF binding region
ENSG00000258418	CpG island
ENSG00000258480	CpG island
ENSG00000258480	chromatin interactions

Extended variants
information (count: 2278 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2278 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190906432	chr14:40761032-40761033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1955550	chr14:40761036-40761037	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs183094210	chr14:40761044-40761045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4638475	chr14:40761051-40761052	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs8006469	chr14:40761094-40761095	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs531411148	chr14:40761131-40761132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567795713	chr14:40761136-40761137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551093814	chr14:40761155-40761156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs58307058	chr14:40761176-40761177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550258972	chr14:40761194-40761195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527282463	chr14:40761223-40761224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569903527	chr14:40761228-40761229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546937495	chr14:40761240-40761241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142426512	chr14:40761242-40761243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566966073	chr14:40761248-40761249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146657794	chr14:40761281-40761282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555894776	chr14:40761336-40761337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556359236	chr14:40761338-40761339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144991246	chr14:40761351-40761352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4903573	chr14:40761373-40761374	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs554049683	chr14:40761418-40761419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186713122	chr14:40761420-40761421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs578098801	chr14:40761430-40761431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540611112	chr14:40761449-40761450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149075858	chr14:40761456-40761457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573952408	chr14:40761470-40761471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575563411	chr14:40761528-40761529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115088508	chr14:40761541-40761542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565820357	chr14:40761566-40761567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562657230	chr14:40761572-40761573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531317593	chr14:40761593-40761594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116240565	chr14:40761618-40761619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73288363	chr14:40761627-40761628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564263980	chr14:40761638-40761639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4903574	chr14:40761724-40761725	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs566838090	chr14:40761732-40761733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529563338	chr14:40761806-40761807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141804165	chr14:40761834-40761835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535940799	chr14:40761857-40761858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569389969	chr14:40761879-40761880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554463395	chr14:40761882-40761883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs58587193	chr14:40761902-40761903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201242874	chr14:40761903-40761904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558329564	chr14:40761973-40761974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543121693	chr14:40761994-40761995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191172759	chr14:40762041-40762042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115341607	chr14:40762077-40762078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143142361	chr14:40762089-40762090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148260118	chr14:40762091-40762092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536506195	chr14:40762107-40762108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
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
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
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	19805367	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:40761000-40763600	Enhancers	Primary B cells from cord blood	blood
2	chr14:40761400-40761600	Enhancers	Primary B cells from peripheral blood	blood
3	chr14:40761600-40762200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr14:40762200-40763400	Enhancers	Primary B cells from peripheral blood	blood
5	chr14:40763000-40763200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:40777000-40777200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:40777000-40777200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr14:40777000-40787400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr14:40782000-40782400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:40787400-40788000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr14:40787400-40788000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr14:40787400-40788000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr14:40787600-40788000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr14:40794600-40794800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr14:40794600-40795400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr14:40794800-40796200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr14:40795000-40795200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr14:40795000-40795800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr14:40795200-40795800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr14:40795200-40796000	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr14:40795400-40795800	Active TSS	H1 Cell Line	embryonic stem cell
22	chr14:40795400-40795800	Enhancers	H9 Cell Line	embryonic stem cell
23	chr14:40795400-40796000	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr14:40795400-40796000	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr14:40795600-40796200	Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr14:40795800-40796200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr14:40795800-40801600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr14:40796000-40801600	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr14:40801600-40801800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr14:40801600-40802200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
31	chr14:40801800-40806000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr14:40805000-40806600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr14:40805200-40806600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr14:40805400-40806600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:40805400-40806800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr14:40805600-40806200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr14:40805600-40806600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr14:40806000-40806400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr14:40806000-40806400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr14:40806200-40806400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr14:40806200-40809600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr14:40806400-40809600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr14:40806400-40809600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr14:40806400-40816000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:40806600-40809600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr14:40806600-40809600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr14:40806800-40809600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr14:40809200-40810800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr14:40809600-40810200	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr14:40809600-40810200	Enhancers	HUES48 Cell Line	embryonic stem cell

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