Variant report

Variant	nsv523709
Chromosome Location	chr11:4476699-4540077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:543)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:4514547-4514747	K562	blood:	n/a	n/a
2	ATF1	chr11:4502329-4502511	K562	blood:	n/a	n/a
3	ATF3	chr11:4502231-4502443	K562	blood:	n/a	n/a
4	ATF3	chr11:4494239-4494395	K562	blood:	n/a	n/a
5	BATF	chr11:4514210-4514762	GM12878	blood:	n/a	n/a
6	BATF	chr11:4514308-4514557	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:4514325-4514757	GM12878	blood:	n/a	n/a
8	BCL11A	chr11:4514425-4514768	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:4494212-4494443	K562	blood:	n/a	n/a
10	BHLHE40	chr11:4514088-4514588	K562	blood:	n/a	n/a
11	BHLHE40	chr11:4514262-4514648	GM12878	blood:	n/a	n/a
12	CEBPB	chr11:4480878-4481078	H1-hESC	embryonic stem cell:	n/a	chr11:4480932-4480943
13	CEBPB	chr11:4511868-4512046	K562	blood:	n/a	chr11:4511948-4511959
14	CEBPB	chr11:4506243-4506344	K562	blood:	n/a	n/a
15	CEBPB	chr11:4485526-4486025	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr11:4521549-4521828	K562	blood:	n/a	chr11:4521689-4521700
17	CEBPB	chr11:4484563-4484620	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr11:4511807-4512092	IMR90	lung:	n/a	chr11:4511948-4511959
19	CEBPB	chr11:4521534-4521859	HepG2	liver:	n/a	chr11:4521689-4521700
20	CEBPB	chr11:4511844-4512110	HepG2	liver:	n/a	chr11:4511948-4511959
21	CEBPB	chr11:4480816-4481016	K562	blood:	n/a	chr11:4480932-4480943
22	CEBPB	chr11:4521640-4521844	A549	lung:	n/a	chr11:4521689-4521700
23	CEBPB	chr11:4512084-4512518	MCF-7	breast:	n/a	n/a
24	CEBPB	chr11:4516863-4517063	K562	blood:	n/a	n/a
25	CEBPB	chr11:4480768-4481058	Hela-S3	cervix:	n/a	chr11:4480932-4480943
26	CEBPB	chr11:4511930-4511964	H1-hESC	embryonic stem cell:	n/a	chr11:4511948-4511959
27	CEBPB	chr11:4521600-4521789	H1-hESC	embryonic stem cell:	n/a	chr11:4521689-4521700
28	CEBPB	chr11:4480790-4481073	HepG2	liver:	n/a	chr11:4480932-4480943
29	CEBPB	chr11:4521334-4521828	IMR90	lung:	n/a	chr11:4521689-4521700
30	CEBPB	chr11:4511852-4512146	A549	lung:	n/a	chr11:4511948-4511959
31	CEBPB	chr11:4540065-4540287	HepG2	liver:	n/a	chr11:4540117-4540130
32	CHD1	chr11:4485864-4486172	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr11:4485610-4486013	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr11:4514523-4514800	GM19240	blood:	n/a	n/a
35	CTCF	chr11:4514940-4515090	HMEC	breast:	n/a	n/a
36	CTCF	chr11:4514600-4514750	HCFaa	heart:	n/a	n/a
37	CTCF	chr11:4514580-4514870	AG04450	lung:	n/a	n/a
38	CTCF	chr11:4514841-4514843	Medullo	brain:	n/a	n/a
39	CTCF	chr11:4514461-4514790	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr11:4514465-4514734	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr11:4514522-4514808	Fibrobl	skin:	n/a	n/a
42	CTCF	chr11:4514480-4514630	AG04449	skin:	n/a	n/a
43	CTCF	chr11:4514500-4514650	BE2_C	brain:	n/a	n/a
44	CTCF	chr11:4514547-4514839	Medullo	brain:	n/a	n/a
45	CTCF	chr11:4514760-4514910	K562	blood:	n/a	n/a
46	CTCF	chr11:4515020-4515170	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr11:4514580-4514730	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr11:4514510-4514799	GM12892	blood:	n/a	n/a
49	CTCF	chr11:4514537-4514812	Lung_OC	lung:	n/a	n/a
50	CTCF	chr11:4514940-4515090	HMF	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4508841-4508891	HCT-116	colon:	n/a
2	chr11:4510366-4510416	AG04449	skin:	fetal
3	chr11:4508841-4508891	SK-N-SH	brain:	n/a
4	chr11:4509357-4509407	Hepatocyte	liver:	n/a
5	chr11:4509357-4509407	H1-hESC	embryonic stem cell:	embryo
6	chr11:4508841-4508891	AG04449	skin:	fetal
7	chr11:4509357-4509407	HRPEpiC	eye:	n/a
8	chr11:4508841-4508891	HCPEpiC	choroid plexus:	n/a
9	chr11:4510366-4510416	MCF-7	breast:	n/a
10	chr11:4508841-4508891	HL-60	blood:	n/a
11	chr11:4508841-4508891	NHBE	bronchial:	n/a
12	chr11:4510366-4510416	H1-hESC	embryonic stem cell:	embryo
13	chr11:4509357-4509407	Hela-S3	cervix:	n/a
14	chr11:4509357-4509407	HepG2	liver:	n/a
15	chr11:4509357-4509407	SKMC	muscle:	n/a
16	chr11:4508841-4508891	SAEC	small airway:	n/a
17	chr11:4508841-4508891	LNCaP	prostate:	n/a
18	chr11:4509357-4509407	SAEC	small airway:	n/a
19	chr11:4509357-4509407	AG04449	skin:	fetal
20	chr11:4509357-4509407	LNCaP	prostate:	n/a
21	chr11:4508841-4508891	GM19239	blood:	n/a
22	chr11:4508841-4508891	GM06990	blood:	n/a
23	chr11:4510366-4510416	SKMC	muscle:	n/a
24	chr11:4510366-4510416	GM19239	blood:	n/a
25	chr11:4509357-4509407	CMK	blood:	n/a
26	chr11:4510366-4510416	HEK293	kidney:	embryo
27	chr11:4510366-4510416	HRCEpiC	kidney:	n/a
28	chr11:4508841-4508891	ECC-1	luminal epithelium:	n/a
29	chr11:4510366-4510416	SK-N-SH_RA	brain:	n/a
30	chr11:4509357-4509407	PANC-1	pancreas:	n/a
31	chr11:4509357-4509407	HUVEC	blood vessel:	n/a
32	chr11:4510366-4510416	HRPEpiC	eye:	n/a
33	chr11:4510366-4510416	HEEpiC	esophagus:	n/a
34	chr11:4508841-4508891	Hepatocyte	liver:	n/a
35	chr11:4509357-4509407	ProgFib	skin:	n/a
36	chr11:4510366-4510416	PrEC	prostate:	n/a
37	chr11:4510366-4510416	RPTEC	kidney:	n/a
38	chr11:4509357-4509407	GM12892	blood:	n/a
39	chr11:4510366-4510416	CMK	blood:	n/a
40	chr11:4508841-4508891	NH-A	brain:	n/a
41	chr11:4508841-4508891	HNPCEpiC	eye:	n/a
42	chr11:4508841-4508891	A549	lung:	n/a
43	chr11:4508841-4508891	SKMC	muscle:	n/a
44	chr11:4508841-4508891	BE2_C	brain:	n/a
45	chr11:4509357-4509407	SK-N-MC	brain:	n/a
46	chr11:4510366-4510416	SK-N-MC	brain:	n/a
47	chr11:4509357-4509407	ovcar-3	ovarian:	n/a
48	chr11:4510366-4510416	HRE	kidney:	n/a
49	chr11:4508841-4508891	PrEC	prostate:	n/a
50	chr11:4509357-4509407	PFSK-1	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4531179..4533009-chr11:4535130..4536667,2	K562	blood:
2	chr11:4402110..4404126-chr11:4484207..4486605,2	K562	blood:
3	chr11:4535006..4537782-chr11:4538961..4542552,3	K562	blood:
4	chr11:4208460..4209382-chr11:4513705..4515541,8	MCF-7	breast:
5	chr11:4208123..4209247-chr11:4514343..4515119,4	MCF-7	breast:
6	chr11:4531179..4533009-chr11:4535130..4536667,2	K562	blood:

No data

Variant related genes	Relation type
OR52M2P	TF binding region
OR52K1	TF binding region
OR52K3P	TF binding region
OR52M2P	CpG island
OR52K1	CpG island
OR52K3P	CpG island
ENSG00000226616	chromatin interactions
ENSG00000254480	chromatin interactions

Extended variants
information (count: 2662 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2662 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs331535	chr11:4476699-4476700	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568370233	chr11:4476720-4476721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72854374	chr11:4476731-4476732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530863629	chr11:4476773-4476774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548194957	chr11:4476777-4476778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533348798	chr11:4476786-4476787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186243413	chr11:4476788-4476789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576293581	chr11:4476791-4476792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142624201	chr11:4476823-4476824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139583036	chr11:4476855-4476856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112432995	chr11:4476860-4476861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11032319	chr11:4476880-4476881	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs545101581	chr11:4476894-4476895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73432791	chr11:4476916-4476917	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs386749995	chr11:4476942-4476943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144891909	chr11:4476944-4476945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561602769	chr11:4476951-4476952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147882488	chr11:4476972-4476973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535788689	chr11:4477034-4477035	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs367882928	chr11:4477067-4477068	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs331534	chr11:4477080-4477081	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs140420742	chr11:4477115-4477116	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs11824595	chr11:4477122-4477123	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2115930	chr11:4477195-4477196	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs184990300	chr11:4477217-4477218	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs150431454	chr11:4477254-4477255	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs547906412	chr11:4477261-4477262	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552840250	chr11:4477268-4477269	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs569906826	chr11:4477270-4477271	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs115573690	chr11:4477283-4477284	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs558283269	chr11:4477290-4477291	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs540397196	chr11:4477295-4477296	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs138207029	chr11:4477296-4477297	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs534545553	chr11:4477345-4477346	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs189896422	chr11:4477346-4477347	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs572473392	chr11:4477348-4477349	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs151141666	chr11:4477352-4477353	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs374402866	chr11:4477353-4477354	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs2115931	chr11:4477398-4477399	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs561138698	chr11:4477476-4477477	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs149097422	chr11:4477489-4477490	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs183202732	chr11:4477492-4477493	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs541864659	chr11:4477504-4477505	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187419115	chr11:4477531-4477532	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532746300	chr11:4477535-4477536	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs144751117	chr11:4477538-4477539	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs114405596	chr11:4477545-4477546	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs542558710	chr11:4477561-4477562	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs376349569	chr11:4477562-4477563	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs138776026	chr11:4477563-4477564	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4470800-4480800	Weak transcription	Ovary	ovary
2	chr11:4471600-4481800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:4475400-4478000	Enhancers	Primary B cells from cord blood	blood
4	chr11:4476200-4477400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr11:4476400-4477000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr11:4476600-4477000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr11:4476600-4480200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:4477000-4477400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr11:4477000-4478000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr11:4477200-4477400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:4477400-4480600	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr11:4478000-4481800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr11:4479400-4483800	Enhancers	Fetal Intestine Small	intestine
14	chr11:4480000-4483600	Enhancers	Fetal Intestine Large	intestine
15	chr11:4480200-4481000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr11:4480200-4481000	Enhancers	Adipose Nuclei	Adipose
17	chr11:4480400-4480600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr11:4480400-4481000	Enhancers	Primary B cells from peripheral blood	blood
19	chr11:4480600-4481200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr11:4480600-4481200	Enhancers	HMEC	breast
21	chr11:4480800-4481000	Enhancers	Ovary	ovary
22	chr11:4480800-4481000	Enhancers	Pancreas	Pancrea
23	chr11:4480800-4481800	Enhancers	Left Ventricle	heart
24	chr11:4481000-4481400	Weak transcription	Ovary	ovary
25	chr11:4481000-4485200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:4481200-4482200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr11:4481400-4482400	Enhancers	Ovary	ovary
28	chr11:4481600-4481800	Enhancers	Pancreas	Pancrea
29	chr11:4481800-4483400	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr11:4482200-4484400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr11:4483400-4484200	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr11:4484200-4486200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:4484200-4487000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
34	chr11:4484400-4484600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr11:4484400-4486400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
36	chr11:4484600-4485600	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr11:4484800-4486400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
38	chr11:4485200-4487200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr11:4485600-4485800	ZNF genes & repeats	NHEK	skin
40	chr11:4485600-4487800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr11:4485600-4488600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr11:4485800-4486000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr11:4486000-4490000	Enhancers	Fetal Intestine Small	intestine
44	chr11:4486200-4490200	Enhancers	Fetal Intestine Large	intestine
45	chr11:4486400-4486600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr11:4486400-4487000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr11:4486400-4487400	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr11:4486600-4486800	Enhancers	Primary B cells from peripheral blood	blood
49	chr11:4486600-4487600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr11:4486800-4488400	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links