Variant report

Variant	nsv879520
Chromosome Location	chr4:86829529-86918232
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	ARID3A	chr4:86880781-86881041	K562	blood:	n/a	n/a
2	ARID3A	chr4:86850439-86850920	HepG2	liver:	n/a	n/a
3	ATF1	chr4:86876892-86877189	K562	blood:	n/a	n/a
4	BACH1	chr4:86895963-86896048	K562	blood:	n/a	n/a
5	BATF	chr4:86900366-86900640	GM12878	blood:	n/a	n/a
6	BATF	chr4:86900349-86900625	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:86850104-86850271	GM12878	blood:	n/a	n/a
8	CBX3	chr4:86874604-86875365	HCT-116	colon:	n/a	n/a
9	CCNT2	chr4:86876823-86877089	K562	blood:	n/a	n/a
10	CCNT2	chr4:86885400-86885546	K562	blood:	n/a	n/a
11	CEBPB	chr4:86874724-86875230	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:86875043-86875049	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:86890178-86890468	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:86905831-86906042	HepG2	liver:	n/a	chr4:86905916-86905927
15	CEBPB	chr4:86853310-86853506	H1-hESC	embryonic stem cell:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
16	CEBPB	chr4:86890193-86890453	A549	lung:	n/a	n/a
17	CEBPB	chr4:86905811-86906054	IMR90	lung:	n/a	chr4:86905916-86905927
18	CEBPB	chr4:86874659-86875202	A549	lung:	n/a	n/a
19	CEBPB	chr4:86854541-86854731	HepG2	liver:	n/a	chr4:86854570-86854581 chr4:86854569-86854582 chr4:86854569-86854582
20	CEBPB	chr4:86853236-86853525	IMR90	lung:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
21	CEBPB	chr4:86907477-86907775	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:86831561-86831722	HepG2	liver:	n/a	chr4:86831593-86831604
23	CEBPB	chr4:86873759-86874014	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:86893642-86893937	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:86909520-86909536	A549	lung:	n/a	n/a
26	CEBPB	chr4:86860822-86861044	A549	lung:	n/a	chr4:86860966-86860977
27	CEBPB	chr4:86890166-86890507	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:86893716-86893924	K562	blood:	n/a	n/a
29	CEBPB	chr4:86853257-86853549	A549	lung:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
30	CEBPB	chr4:86909606-86909689	HepG2	liver:	n/a	chr4:86909622-86909633
31	CEBPB	chr4:86873654-86874078	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:86878869-86879143	K562	blood:	n/a	n/a
33	CEBPB	chr4:86874791-86875151	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:86860830-86861051	HepG2	liver:	n/a	chr4:86860966-86860977
35	CEBPB	chr4:86874745-86875108	A549	lung:	n/a	n/a
36	CHD2	chr4:86874708-86875087	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr4:86831032-86831138	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr4:86890160-86890310	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr4:86885581-86885774	Gliobla	brain:	n/a	n/a
40	CTCF	chr4:86890180-86890330	AG04450	lung:	n/a	n/a
41	CTCF	chr4:86890240-86890390	GM12865	blood:	n/a	chr4:86890324-86890340 chr4:86890318-86890339 chr4:86890328-86890336 chr4:86890323-86890341
42	CTCF	chr4:86890175-86890410	A549	lung:	n/a	chr4:86890324-86890340 chr4:86890318-86890339 chr4:86890328-86890336 chr4:86890323-86890341
43	CTCF	chr4:86890130-86890460	H1-hESC	embryonic stem cell:	n/a	chr4:86890324-86890340 chr4:86890318-86890339 chr4:86890328-86890336 chr4:86890323-86890341
44	CTCF	chr4:86885600-86885750	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr4:86885580-86885730	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr4:86890340-86890490	RPTEC	kidney:	n/a	n/a
47	CTCF	chr4:86890247-86890445	GM10248	blood:	n/a	chr4:86890324-86890340 chr4:86890318-86890339 chr4:86890328-86890336 chr4:86890323-86890341
48	CTCF	chr4:86890161-86890471	ECC-1	luminal epithelium:	n/a	chr4:86890324-86890340 chr4:86890318-86890339 chr4:86890328-86890336 chr4:86890323-86890341
49	CTCF	chr4:86890240-86890390	GM12870	blood:	n/a	chr4:86890324-86890340 chr4:86890318-86890339 chr4:86890328-86890336 chr4:86890323-86890341
50	CTCF	chr4:86885693-86885730	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:86851225-86851275	HIPEpiC	eye:	n/a
2	chr4:86851225-86851275	HIPEpiC	eye:	n/a
3	chr4:86850721-86850771	K562	blood:	n/a
4	chr4:86851425-86851475	BE2_C	brain:	n/a
5	chr4:86851225-86851275	PrEC	prostate:	n/a
6	chr4:86850721-86850771	BJ	skin:	n/a
7	chr4:86852666-86852716	GM12892	blood:	n/a
8	chr4:86874205-86874255	IMR90	lung:	fetal
9	chr4:86874205-86874255	HUVEC	blood vessel:	n/a
10	chr4:86850721-86850771	HNPCEpiC	eye:	n/a
11	chr4:86874205-86874255	MCF10A-Er-Src	breast:	n/a
12	chr4:86852666-86852716	HAEpiC	amniotic membrane:	n/a
13	chr4:86851225-86851275	HCM	heart:	n/a
14	chr4:86851399-86851449	MCF-7	breast:	n/a
15	chr4:86851225-86851275	PFSK-1	brain:	n/a
16	chr4:86851411-86851461	AG04450	lung:	fetal
17	chr4:86852666-86852716	ProgFib	skin:	n/a
18	chr4:86850721-86850771	HEEpiC	esophagus:	n/a
19	chr4:86851425-86851475	Hela-S3	cervix:	n/a
20	chr4:86852666-86852716	AG09319	gingival:	n/a
21	chr4:86874205-86874255	GM12878	blood:	n/a
22	chr4:86851425-86851475	IMR90	lung:	fetal
23	chr4:86850721-86850771	AG09309	skin:	n/a
24	chr4:86850721-86850771	IMR90	lung:	fetal
25	chr4:86851399-86851449	HCF	heart:	n/a
26	chr4:86874205-86874255	ProgFib	skin:	n/a
27	chr4:86851225-86851275	MCF-7	breast:	n/a
28	chr4:86851411-86851461	IMR90	lung:	fetal
29	chr4:86851425-86851475	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:86850721-86850771	HL-60	blood:	n/a
31	chr4:86851411-86851461	HL-60	blood:	n/a
32	chr4:86851425-86851475	HRCEpiC	kidney:	n/a
33	chr4:86852666-86852716	HMEC	breast:	n/a
34	chr4:86851411-86851461	GM12878	blood:	n/a
35	chr4:86851425-86851475	GM12891	blood:	n/a
36	chr4:86851411-86851461	SK-N-MC	brain:	n/a
37	chr4:86851399-86851449	U87	brain:	n/a
38	chr4:86851425-86851475	LNCaP	prostate:	n/a
39	chr4:86851411-86851461	NHDF-neo	bronchial:	n/a
40	chr4:86851411-86851461	NT2-D1	testis:	n/a
41	chr4:86874205-86874255	HEK293	kidney:	embryo
42	chr4:86852666-86852716	MCF-7	breast:	n/a
43	chr4:86874205-86874255	HepG2	liver:	n/a
44	chr4:86851425-86851475	HEK293	kidney:	embryo
45	chr4:86874205-86874255	HRE	kidney:	n/a
46	chr4:86851411-86851461	HNPCEpiC	eye:	n/a
47	chr4:86851411-86851461	HAEpiC	amniotic membrane:	n/a
48	chr4:86851411-86851461	HUVEC	blood vessel:	n/a
49	chr4:86852666-86852716	HEK293	kidney:	embryo
50	chr4:86850721-86850771	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:86747130..86748178-chr4:86885197..86886140,3	MCF-7	breast:
2	chr4:86717774..86718537-chr4:86886876..86887427,3	MCF-7	breast:
3	chr4:86717573..86718676-chr4:86889897..86890637,3	MCF-7	breast:
4	chr4:86858002..86860369-chr4:86861620..86863403,2	K562	blood:
5	chr4:86717884..86718437-chr4:86885535..86886084,2	MCF-7	breast:
6	chr4:86851168..86853730-chr4:86855449..86857714,2	K562	blood:
7	chr4:86881196..86882931-chr4:86883765..86885876,2	K562	blood:
8	chr4:86853756..86855558-chr4:86856892..86859472,2	K562	blood:
9	chr4:86858002..86860369-chr4:86861620..86863403,2	K562	blood:
10	chr4:86855216..86857997-chr4:86860601..86862726,2	K562	blood:
11	chr4:86717537..86719169-chr4:86889518..86891294,13	MCF-7	breast:
12	chr4:86717783..86718591-chr4:86885186..86885920,6	MCF-7	breast:
13	chr4:86855216..86857997-chr4:86860601..86862726,2	K562	blood:
14	chr4:86855497..86859080-chr4:86873833..86876584,3	MCF-7	breast:
15	chr4:86829743..86832305-chr4:86837536..86839356,2	MCF-7	breast:
16	chr4:86678039..86678782-chr4:86890252..86890768,2	MCF-7	breast:
17	chr4:86855497..86859080-chr4:86873833..86876584,3	MCF-7	breast:
18	chr4:86853756..86855558-chr4:86856892..86859472,2	K562	blood:
19	chr4:86881196..86882931-chr4:86883765..86885876,2	K562	blood:

Variant related genes	Relation type
ENSG00000265774	TF binding region
ARHGAP24	TF binding region
ENSG00000265774	CpG island
ARHGAP24	CpG island
ENSG00000138639	chromatin interactions
ENSG00000265774	chromatin interactions

Extended variants
information (count: 3116 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3116 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7696763	chr4:86829529-86829530	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570871700	chr4:86829545-86829546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9997854	chr4:86829569-86829570	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs182270373	chr4:86829585-86829586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544258698	chr4:86829653-86829654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374206799	chr4:86829659-86829660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562936219	chr4:86829696-86829697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146422658	chr4:86829761-86829762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545666024	chr4:86829806-86829807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564043422	chr4:86829865-86829866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528233185	chr4:86829888-86829889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546431399	chr4:86829899-86829900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186540346	chr4:86829914-86829915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529015611	chr4:86829929-86829930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550293841	chr4:86830018-86830019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17011177	chr4:86830058-86830059	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs539441236	chr4:86830114-86830115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552060437	chr4:86830116-86830117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140947921	chr4:86830133-86830134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114853892	chr4:86830144-86830145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374194559	chr4:86830330-86830331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555954271	chr4:86830333-86830334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373250035	chr4:86830450-86830451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs386676906	chr4:86830455-86830456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538303062	chr4:86830456-86830457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556403546	chr4:86830463-86830464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143254418	chr4:86830518-86830519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78031604	chr4:86830537-86830538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542428157	chr4:86830574-86830575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564031204	chr4:86830604-86830605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192536672	chr4:86830626-86830627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148880552	chr4:86830632-86830633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185380817	chr4:86830665-86830666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs386676907	chr4:86830682-86830683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529095119	chr4:86830710-86830711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566265676	chr4:86830724-86830725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550601336	chr4:86830738-86830739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535079261	chr4:86830750-86830751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376865616	chr4:86830878-86830879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190425391	chr4:86830919-86830920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116160327	chr4:86830933-86830934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551441164	chr4:86830935-86830936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567147963	chr4:86830938-86830939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7434916	chr4:86830941-86830942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs28605002	chr4:86831004-86831005	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549427173	chr4:86831029-86831030	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs192887121	chr4:86831030-86831031	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs77616387	chr4:86831036-86831037	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs556580814	chr4:86831052-86831053	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs571448815	chr4:86831070-86831071	Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	20459617	CNVD

Chromatin state (count:1321 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86790800-86835400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr4:86791200-86844400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:86808200-86846000	Weak transcription	HUVEC	blood vessel
4	chr4:86812200-86831200	Weak transcription	Primary B cells from peripheral blood	blood
5	chr4:86812400-86831000	Weak transcription	Fetal Muscle Leg	muscle
6	chr4:86815800-86831000	Weak transcription	Fetal Muscle Trunk	muscle
7	chr4:86815800-86842800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:86818000-86831000	Weak transcription	Pancreas	Pancrea
9	chr4:86818400-86831200	Weak transcription	Right Ventricle	heart
10	chr4:86823800-86832400	Weak transcription	NHDF-Ad	bronchial
11	chr4:86825600-86831000	Weak transcription	Left Ventricle	heart
12	chr4:86826400-86830600	Weak transcription	Adipose Nuclei	Adipose
13	chr4:86826800-86845400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:86827200-86831000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:86827400-86831000	Weak transcription	Duodenum Mucosa	Duodenum
16	chr4:86827400-86834200	Weak transcription	Stomach Mucosa	stomach
17	chr4:86827600-86835400	Weak transcription	Small Intestine	intestine
18	chr4:86827600-86850600	Weak transcription	Spleen	Spleen
19	chr4:86828200-86831000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr4:86828200-86831200	Weak transcription	Ovary	ovary
21	chr4:86828600-86829600	Strong transcription	Primary B cells from cord blood	blood
22	chr4:86828800-86830200	Weak transcription	Fetal Kidney	kidney
23	chr4:86828800-86834000	Weak transcription	Fetal Intestine Large	intestine
24	chr4:86828800-86834200	Weak transcription	Fetal Intestine Small	intestine
25	chr4:86829600-86831000	Weak transcription	Gastric	stomach
26	chr4:86829600-86843800	Weak transcription	Primary B cells from cord blood	blood
27	chr4:86830200-86830800	Enhancers	Fetal Kidney	kidney
28	chr4:86830600-86831600	Enhancers	Adipose Nuclei	Adipose
29	chr4:86830800-86834400	Weak transcription	Fetal Kidney	kidney
30	chr4:86831000-86831200	Enhancers	Aorta	Aorta
31	chr4:86831000-86831200	Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr4:86831000-86831400	Enhancers	Left Ventricle	heart
33	chr4:86831000-86831400	Enhancers	Lung	lung
34	chr4:86831000-86831400	Enhancers	Right Atrium	heart
35	chr4:86831000-86831400	Enhancers	HMEC	breast
36	chr4:86831000-86831600	Active TSS	Duodenum Mucosa	Duodenum
37	chr4:86831000-86831600	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr4:86831000-86831800	Enhancers	Brain Anterior Caudate	brain
39	chr4:86831000-86832000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr4:86831000-86832200	Enhancers	Fetal Muscle Leg	muscle
41	chr4:86831000-86832400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:86831000-86832400	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr4:86831000-86832400	Enhancers	Fetal Muscle Trunk	muscle
44	chr4:86831000-86832400	Enhancers	Pancreas	Pancrea
45	chr4:86831000-86832600	Enhancers	Gastric	stomach
46	chr4:86831200-86831400	Strong transcription	Primary B cells from peripheral blood	blood
47	chr4:86831200-86831400	Enhancers	Brain Cingulate Gyrus	brain
48	chr4:86831200-86831400	Enhancers	Esophagus	oesophagus
49	chr4:86831200-86831400	Enhancers	Ovary	ovary
50	chr4:86831200-86831400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle

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