Variant report

Variant	nsv879540
Chromosome Location	chr4:91156104-91212092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:118)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:118 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:91203800-91204076	Hela-S3	cervix:	n/a	chr4:91203939-91203950
2	CEBPB	chr4:91203815-91204120	HepG2	liver:	n/a	chr4:91203939-91203950
3	CEBPB	chr4:91203839-91204076	A549	lung:	n/a	chr4:91203939-91203950
4	CEBPB	chr4:91203845-91204042	H1-hESC	embryonic stem cell:	n/a	chr4:91203939-91203950
5	CTCF	chr4:91161600-91161750	BE2_C	brain:	n/a	n/a
6	CTCF	chr4:91161472-91161769	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr4:91210100-91210250	GM12864	blood:	n/a	n/a
8	CTCF	chr4:91195140-91195290	K562	blood:	n/a	n/a
9	CTCF	chr4:91184600-91184750	GM12873	blood:	n/a	n/a
10	CTCF	chr4:91161640-91161678	GM19238	blood:	n/a	n/a
11	CTCF	chr4:91188285-91188326	Fibrobl	skin:	n/a	n/a
12	CTCF	chr4:91161660-91161810	MCF-7	breast:	n/a	n/a
13	CTCF	chr4:91161620-91161770	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr4:91201500-91201650	HVMF	connective:	n/a	n/a
15	CTCF	chr4:91161558-91161796	GM12878	blood:	n/a	n/a
16	CTCF	chr4:91161540-91161690	HEK293	kidney:	n/a	n/a
17	CTCF	chr4:91161604-91161727	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr4:91161560-91161710	GM12878	blood:	n/a	n/a
19	CTCF	chr4:91161459-91161849	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr4:91161580-91161730	BE2_C	brain:	n/a	n/a
21	CTCF	chr4:91161660-91161810	GM12873	blood:	n/a	n/a
22	CTCF	chr4:91161621-91161724	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:91180638-91180718	LNCaP	prostate:	n/a	n/a
24	CTCF	chr4:91161622-91161709	MCF-7	breast:	n/a	n/a
25	E2F4	chr4:91196217-91196398	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr4:91211223-91211412	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr4:91177319-91177479	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr4:91168163-91168365	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr4:91162301-91162390	GM12878	blood:	n/a	n/a
30	EP300	chr4:91155455-91156925	SK-N-SH	brain:	n/a	chr4:91156719-91156733
31	EP300	chr4:91211994-91212896	SK-N-SH	brain:	n/a	chr4:91212000-91212014
32	EP300	chr4:91156035-91156470	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr4:91156074-91156509	SK-N-SH_RA	brain:	n/a	n/a
34	FOS	chr4:91202685-91203141	MCF10A-Er-Src	breast:	n/a	chr4:91203038-91203049 chr4:91203042-91203050
35	FOS	chr4:91210885-91211204	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:91202608-91203189	MCF10A-Er-Src	breast:	n/a	chr4:91203038-91203049 chr4:91203042-91203050
37	FOS	chr4:91168066-91168394	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:91168057-91168434	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:91210947-91211196	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:91168090-91168369	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:91210891-91211128	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:91210939-91211190	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:91168076-91168421	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr4:91202657-91203242	MCF10A-Er-Src	breast:	n/a	chr4:91203038-91203049 chr4:91203042-91203050
45	FOS	chr4:91202576-91203232	MCF10A-Er-Src	breast:	n/a	chr4:91203038-91203049 chr4:91203042-91203050
46	FOS	chr4:91177428-91177457	MCF10A-Er-Src	breast:	n/a	n/a
47	GATA2	chr4:91155975-91156692	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr4:91191150-91191523	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr4:91180884-91180966	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr4:91156193-91156427	T-47D	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	chr4:91156290-91156340	HepG2	liver:	n/a
2	chr4:91156155-91156205	H1-hESC	embryonic stem cell:	embryo
3	chr4:91156113-91156163	A549	lung:	n/a
4	chr4:91156113-91156163	SK-N-SH	brain:	n/a
5	chr4:91156113-91156163	HMEC	breast:	n/a
6	chr4:91156290-91156340	HCM	heart:	n/a
7	chr4:91156113-91156163	Jurkat	blood:	n/a
8	chr4:91156113-91156163	IMR90	lung:	fetal
9	chr4:91156155-91156205	HNPCEpiC	eye:	n/a
10	chr4:91156155-91156205	AG04449	skin:	fetal
11	chr4:91156290-91156340	Hela-S3	cervix:	n/a
12	chr4:91156113-91156163	GM12891	blood:	n/a
13	chr4:91156113-91156163	NT2-D1	testis:	n/a
14	chr4:91156155-91156205	CMK	blood:	n/a
15	chr4:91156155-91156205	U87	brain:	n/a
16	chr4:91156155-91156205	AG04450	lung:	fetal
17	chr4:91156290-91156340	BJ	skin:	n/a
18	chr4:91156290-91156340	RPTEC	kidney:	n/a
19	chr4:91156290-91156340	SK-N-SH_RA	brain:	n/a
20	chr4:91156113-91156163	Hela-S3	cervix:	n/a
21	chr4:91156113-91156163	ovcar-3	ovarian:	n/a
22	chr4:91156290-91156340	HNPCEpiC	eye:	n/a
23	chr4:91156113-91156163	Hepatocyte	liver:	n/a
24	chr4:91156113-91156163	SK-N-SH_RA	brain:	n/a
25	chr4:91156113-91156163	ProgFib	skin:	n/a
26	chr4:91156113-91156163	T-47D	breast:	n/a
27	chr4:91156290-91156340	U87	brain:	n/a
28	chr4:91156155-91156205	HL-60	blood:	n/a
29	chr4:91156113-91156163	BE2_C	brain:	n/a
30	chr4:91156155-91156205	HRPEpiC	eye:	n/a
31	chr4:91156155-91156205	Jurkat	blood:	n/a
32	chr4:91156290-91156340	NH-A	brain:	n/a
33	chr4:91156290-91156340	GM06990	blood:	n/a
34	chr4:91156113-91156163	RPTEC	kidney:	n/a
35	chr4:91156155-91156205	AG09309	skin:	n/a
36	chr4:91156113-91156163	GM12878	blood:	n/a
37	chr4:91156113-91156163	HNPCEpiC	eye:	n/a
38	chr4:91156290-91156340	HCPEpiC	choroid plexus:	n/a
39	chr4:91156113-91156163	HCM	heart:	n/a
40	chr4:91156290-91156340	HRCEpiC	kidney:	n/a
41	chr4:91156290-91156340	Hepatocyte	liver:	n/a
42	chr4:91156113-91156163	MCF-7	breast:	n/a
43	chr4:91156290-91156340	CMK	blood:	n/a
44	chr4:91156290-91156340	HRPEpiC	eye:	n/a
45	chr4:91156113-91156163	SKMC	muscle:	n/a
46	chr4:91156155-91156205	A549	lung:	n/a
47	chr4:91156290-91156340	K562	blood:	n/a
48	chr4:91156290-91156340	T-47D	breast:	n/a
49	chr4:91156155-91156205	Hela-S3	cervix:	n/a
50	chr4:91156155-91156205	AG09319	gingival:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:91048643..91051024-chr4:91179121..91181486,2	MCF-7	breast:
2	chr4:91047274..91050081-chr4:91174126..91176725,3	MCF-7	breast:
3	chr4:91047666..91049579-chr4:91159621..91163090,3	MCF-7	breast:
4	chr4:91048863..91050461-chr4:91183370..91185880,2	MCF-7	breast:
5	chr4:91047797..91050906-chr4:91208827..91216551,11	MCF-7	breast:
6	chr4:91048019..91050681-chr4:91168667..91171182,2	MCF-7	breast:
7	chr4:91048337..91050046-chr4:91171503..91174117,2	MCF-7	breast:
8	chr4:91047768..91049636-chr4:91206684..91208393,2	MCF-7	breast:
9	chr4:91047990..91050021-chr4:91202743..91205801,3	MCF-7	breast:
10	chr4:91184499..91186906-chr4:91187123..91189039,2	MCF-7	breast:
11	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
12	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
13	chr4:91184499..91186906-chr4:91187123..91189039,2	MCF-7	breast:
14	chr4:91046902..91051153-chr4:91157807..91162298,6	MCF-7	breast:
15	chr4:91049244..91050799-chr4:91210980..91212924,2	MCF-7	breast:
16	chr4:91081506..91083784-chr4:91211586..91214235,2	MCF-7	breast:

No data

Variant related genes	Relation type
CCSER1	TF binding region
CCSER1	CpG island
ENSG00000184305	chromatin interactions

Extended variants
information (count: 1563 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1563 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs919579	chr4:91156104-91156105	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531660894	chr4:91156109-91156110	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375874010	chr4:91156117-91156118	Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs144205856	chr4:91156137-91156138	Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs527892876	chr4:91156138-91156139	Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs62312863	chr4:91156151-91156152	Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs139858629	chr4:91156201-91156202	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537016488	chr4:91156206-91156207	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548063457	chr4:91156278-91156279	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558689666	chr4:91156325-91156326	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576974438	chr4:91156343-91156344	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567891046	chr4:91156359-91156360	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528863079	chr4:91156369-91156370	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151155678	chr4:91156390-91156391	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534702918	chr4:91156433-91156434	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140084174	chr4:91156489-91156490	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537894166	chr4:91156498-91156499	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115020810	chr4:91156506-91156507	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571457131	chr4:91156550-91156551	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533793304	chr4:91156572-91156573	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554013098	chr4:91156574-91156575	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1431022	chr4:91156595-91156596	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs188238350	chr4:91156609-91156610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376803153	chr4:91156614-91156615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372940458	chr4:91156718-91156719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541774724	chr4:91156750-91156751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181299765	chr4:91156795-91156796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369082044	chr4:91156805-91156806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186156681	chr4:91156840-91156841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563567630	chr4:91156856-91156857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545061360	chr4:91156869-91156870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565081274	chr4:91156874-91156875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572575425	chr4:91156889-91156890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4356886	chr4:91156917-91156918	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs561544960	chr4:91156950-91156951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191961173	chr4:91157022-91157023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149967108	chr4:91157054-91157055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562427122	chr4:91157057-91157058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531374243	chr4:91157201-91157202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181865922	chr4:91157215-91157216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10009936	chr4:91157248-91157249	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186886677	chr4:91157290-91157291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564131394	chr4:91157309-91157310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528611926	chr4:91157313-91157314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373506966	chr4:91157359-91157360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562181709	chr4:91157367-91157368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567476944	chr4:91157433-91157434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145072570	chr4:91157449-91157450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556050366	chr4:91157454-91157455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541723609	chr4:91157458-91157459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495309	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91155000-91158800	Weak transcription	Fetal Intestine Small	intestine
2	chr4:91155800-91156400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr4:91155800-91156600	Active TSS	Brain Germinal Matrix	brain
4	chr4:91155800-91156600	Enhancers	Fetal Heart	heart
5	chr4:91156000-91156200	Enhancers	Adipose Nuclei	Adipose
6	chr4:91156000-91156200	Enhancers	Fetal Brain Female	brain
7	chr4:91156000-91156200	Active TSS	Left Ventricle	heart
8	chr4:91156000-91156200	Enhancers	Pancreas	Pancrea
9	chr4:91156000-91156400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:91156000-91156400	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr4:91156000-91156400	Active TSS	Brain Angular Gyrus	brain
12	chr4:91156000-91156400	Active TSS	Brain Hippocampus Middle	brain
13	chr4:91156000-91156400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr4:91156000-91156400	Enhancers	Fetal Brain Male	brain
15	chr4:91156000-91156400	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr4:91156000-91156600	Active TSS	Brain Anterior Caudate	brain
17	chr4:91156000-91156600	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr4:91156000-91156600	Active TSS	Right Atrium	heart
19	chr4:91156000-91156600	Active TSS	Right Ventricle	heart
20	chr4:91156000-91156600	Enhancers	NHEK	skin
21	chr4:91156200-91156400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:91156200-91156400	Enhancers	Fetal Kidney	kidney
23	chr4:91156200-91156400	Flanking Active TSS	Left Ventricle	heart
24	chr4:91156200-91156400	Flanking Active TSS	Pancreas	Pancrea
25	chr4:91156200-91156600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:91156200-91156600	Flanking Active TSS	Adipose Nuclei	Adipose
27	chr4:91156200-91156600	Active TSS	Brain Cingulate Gyrus	brain
28	chr4:91156200-91156600	Flanking Active TSS	Fetal Brain Female	brain
29	chr4:91156200-91156600	Enhancers	Fetal Lung	lung
30	chr4:91156400-91156600	Enhancers	Brain Angular Gyrus	brain
31	chr4:91156400-91156600	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr4:91156400-91156600	Active TSS	Left Ventricle	heart
33	chr4:91156400-91160400	Weak transcription	Fetal Kidney	kidney
34	chr4:91157200-91157400	Enhancers	Brain Hippocampus Middle	brain
35	chr4:91157200-91157400	Enhancers	Right Ventricle	heart
36	chr4:91158400-91159400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:91158800-91159200	Enhancers	Fetal Intestine Small	intestine
38	chr4:91160400-91160600	Enhancers	Fetal Kidney	kidney
39	chr4:91165200-91166000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr4:91165600-91168400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:91167200-91168600	Enhancers	Stomach Mucosa	stomach
42	chr4:91168000-91168400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:91168400-91175400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:91168600-91169600	Weak transcription	Stomach Mucosa	stomach
45	chr4:91169600-91169800	Enhancers	Stomach Mucosa	stomach
46	chr4:91175200-91176000	Enhancers	NHEK	skin
47	chr4:91175400-91175800	Enhancers	Pancreas	Pancrea
48	chr4:91175400-91176000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr4:91175400-91176000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:91175600-91176000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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