Variant report

Variant	nsv879541
Chromosome Location	chr4:91156104-91253355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:91236261-91236570	GM12878	blood:	n/a	n/a
2	BRCA1	chr4:91238929-91239243	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr4:91239486-91239738	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr4:91238211-91238762	HCT-116	colon:	n/a	chr4:91238334-91238345
5	CBX3	chr4:91238989-91239820	HCT-116	colon:	n/a	chr4:91239347-91239358
6	CBX3	chr4:91238930-91239691	HCT-116	colon:	n/a	chr4:91239347-91239358
7	CEBPB	chr4:91238409-91239788	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:91226887-91227069	H1-hESC	embryonic stem cell:	n/a	chr4:91227035-91227046
9	CEBPB	chr4:91247168-91247342	H1-hESC	embryonic stem cell:	n/a	chr4:91247181-91247192 chr4:91247179-91247192
10	CEBPB	chr4:91238825-91239739	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:91226884-91227188	A549	lung:	n/a	chr4:91227035-91227046
12	CEBPB	chr4:91249633-91249946	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:91203845-91204042	H1-hESC	embryonic stem cell:	n/a	chr4:91203939-91203950
14	CEBPB	chr4:91227009-91227119	K562	blood:	n/a	chr4:91227035-91227046
15	CEBPB	chr4:91249649-91249990	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:91203800-91204076	Hela-S3	cervix:	n/a	chr4:91203939-91203950
17	CEBPB	chr4:91226892-91227190	HepG2	liver:	n/a	chr4:91227035-91227046
18	CEBPB	chr4:91226886-91227214	IMR90	lung:	n/a	chr4:91227035-91227046
19	CEBPB	chr4:91247140-91247311	IMR90	lung:	n/a	chr4:91247181-91247192 chr4:91247179-91247192
20	CEBPB	chr4:91238812-91239947	HCT-116	colon:	n/a	n/a
21	CEBPB	chr4:91238800-91239847	HCT-116	colon:	n/a	n/a
22	CEBPB	chr4:91203815-91204120	HepG2	liver:	n/a	chr4:91203939-91203950
23	CEBPB	chr4:91203839-91204076	A549	lung:	n/a	chr4:91203939-91203950
24	CHD2	chr4:91238912-91239210	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr4:91214580-91214730	GM12872	blood:	n/a	n/a
26	CTCF	chr4:91236251-91236266	GM20000	blood:	n/a	n/a
27	CTCF	chr4:91236295-91236549	HUVEC	blood vessel:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
28	CTCF	chr4:91214600-91214750	GM12871	blood:	n/a	n/a
29	CTCF	chr4:91236340-91236490	GM12864	blood:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
30	CTCF	chr4:91236360-91236510	BE2_C	brain:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
31	CTCF	chr4:91214580-91214730	HMF	breast:	n/a	n/a
32	CTCF	chr4:91214530-91214766	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr4:91214591-91214725	A549	lung:	n/a	n/a
34	CTCF	chr4:91236320-91236470	GM12870	blood:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
35	CTCF	chr4:91214580-91214730	GM12869	blood:	n/a	n/a
36	CTCF	chr4:91236136-91236667	MCF-7	breast:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
37	CTCF	chr4:91236360-91236510	HCFaa	heart:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
38	CTCF	chr4:91214580-91214730	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr4:91214580-91214730	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr4:91184600-91184750	GM12873	blood:	n/a	n/a
41	CTCF	chr4:91236360-91236510	HPF	lung:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
42	CTCF	chr4:91236360-91236510	AG10803	skin:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
43	CTCF	chr4:91214620-91214770	AG10803	skin:	n/a	n/a
44	CTCF	chr4:91236297-91236536	LNCaP	prostate:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
45	CTCF	chr4:91236360-91236510	GM12878	blood:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
46	CTCF	chr4:91236053-91236762	A549	lung:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
47	CTCF	chr4:91161604-91161727	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:91236380-91236530	A549	lung:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
49	CTCF	chr4:91236283-91236547	Gliobla	brain:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423
50	CTCF	chr4:91236360-91236510	K562	blood:	n/a	chr4:91236406-91236422 chr4:91236410-91236418 chr4:91236407-91236428 chr4:91236405-91236423

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:91156113-91156163	NB4	blood:	n/a
2	chr4:91156155-91156205	ovcar-3	ovarian:	n/a
3	chr4:91156155-91156205	H1-hESC	embryonic stem cell:	embryo
4	chr4:91156290-91156340	BE2_C	brain:	n/a
5	chr4:91156113-91156163	HL-60	blood:	n/a
6	chr4:91156113-91156163	NT2-D1	testis:	n/a
7	chr4:91156155-91156205	GM19239	blood:	n/a
8	chr4:91156113-91156163	HUVEC	blood vessel:	n/a
9	chr4:91156113-91156163	HCPEpiC	choroid plexus:	n/a
10	chr4:91156155-91156205	SK-N-SH	brain:	n/a
11	chr4:91156290-91156340	HNPCEpiC	eye:	n/a
12	chr4:91156113-91156163	NHDF-neo	bronchial:	n/a
13	chr4:91156155-91156205	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:91156290-91156340	ECC-1	luminal epithelium:	n/a
15	chr4:91156155-91156205	HAEpiC	amniotic membrane:	n/a
16	chr4:91156113-91156163	HIPEpiC	eye:	n/a
17	chr4:91156290-91156340	HIPEpiC	eye:	n/a
18	chr4:91156290-91156340	HAEpiC	amniotic membrane:	n/a
19	chr4:91156155-91156205	CMK	blood:	n/a
20	chr4:91156155-91156205	HEK293	kidney:	embryo
21	chr4:91156113-91156163	GM19239	blood:	n/a
22	chr4:91156290-91156340	GM19239	blood:	n/a
23	chr4:91156113-91156163	HRPEpiC	eye:	n/a
24	chr4:91156113-91156163	HRE	kidney:	n/a
25	chr4:91156290-91156340	HRCEpiC	kidney:	n/a
26	chr4:91156155-91156205	ECC-1	luminal epithelium:	n/a
27	chr4:91156290-91156340	RPTEC	kidney:	n/a
28	chr4:91156113-91156163	MCF10A-Er-Src	breast:	n/a
29	chr4:91156290-91156340	NT2-D1	testis:	n/a
30	chr4:91156155-91156205	HRE	kidney:	n/a
31	chr4:91156290-91156340	ProgFib	skin:	n/a
32	chr4:91156290-91156340	IMR90	lung:	fetal
33	chr4:91156155-91156205	LNCaP	prostate:	n/a
34	chr4:91156155-91156205	SKMC	muscle:	n/a
35	chr4:91156155-91156205	SK-N-SH_RA	brain:	n/a
36	chr4:91156155-91156205	HCPEpiC	choroid plexus:	n/a
37	chr4:91156155-91156205	HRCEpiC	kidney:	n/a
38	chr4:91156290-91156340	NHBE	bronchial:	n/a
39	chr4:91156113-91156163	HEEpiC	esophagus:	n/a
40	chr4:91156155-91156205	AG04450	lung:	fetal
41	chr4:91156155-91156205	AoSMC	blood vessel:	n/a
42	chr4:91156113-91156163	A549	lung:	n/a
43	chr4:91156113-91156163	PrEC	prostate:	n/a
44	chr4:91156290-91156340	HL-60	blood:	n/a
45	chr4:91156155-91156205	RPTEC	kidney:	n/a
46	chr4:91156290-91156340	Jurkat	blood:	n/a
47	chr4:91156290-91156340	PrEC	prostate:	n/a
48	chr4:91156113-91156163	HAEpiC	amniotic membrane:	n/a
49	chr4:91156155-91156205	AG10803	skin:	n/a
50	chr4:91156155-91156205	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:91081506..91083784-chr4:91211586..91214235,2	MCF-7	breast:
2	chr4:91047768..91049636-chr4:91206684..91208393,2	MCF-7	breast:
3	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
4	chr4:91049244..91050799-chr4:91210980..91212924,2	MCF-7	breast:
5	chr10:15280129..15280852-chr4:91229350..91230248,2	MCF-7	breast:
6	chr4:91048863..91050461-chr4:91183370..91185880,2	MCF-7	breast:
7	chr4:91073236..91073889-chr4:91214194..91215162,2	MCF-7	breast:
8	chr4:90952233..90952750-chr4:91214459..91215033,2	MCF-7	breast:
9	chr4:91169608..91171320-chr4:91173409..91175052,2	MCF-7	breast:
10	chr4:91047666..91049579-chr4:91159621..91163090,3	MCF-7	breast:
11	chr4:91047990..91050021-chr4:91202743..91205801,3	MCF-7	breast:
12	chr4:91047274..91050081-chr4:91174126..91176725,3	MCF-7	breast:
13	chr4:91046902..91051153-chr4:91157807..91162298,6	MCF-7	breast:
14	chr4:91048643..91051024-chr4:91179121..91181486,2	MCF-7	breast:
15	chr4:91048337..91050046-chr4:91171503..91174117,2	MCF-7	breast:
16	chr4:91184499..91186906-chr4:91187123..91189039,2	MCF-7	breast:
17	chr4:91047797..91050906-chr4:91208827..91216551,11	MCF-7	breast:
18	chr4:91047211..91049726-chr4:91221351..91224202,2	MCF-7	breast:
19	chr4:91184499..91186906-chr4:91187123..91189039,2	MCF-7	breast:
20	chr4:91048019..91050681-chr4:91168667..91171182,2	MCF-7	breast:

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

Extended variants
information (count: 2888 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2888 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

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:258 , 50 per page) page: 1 2 3 4 5 6

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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