Variant report

Variant	nsv830000
Chromosome Location	chr4:86745341-86909059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1061)
CpG islands
(count:672)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:86850439-86850920	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:86880781-86881041	K562	blood:	n/a	n/a
3	ATF1	chr4:86784098-86784356	K562	blood:	n/a	n/a
4	ATF1	chr4:86876892-86877189	K562	blood:	n/a	n/a
5	BACH1	chr4:86895963-86896048	K562	blood:	n/a	n/a
6	BATF	chr4:86900349-86900625	GM12878	blood:	n/a	n/a
7	BATF	chr4:86900366-86900640	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:86747314-86747693	HepG2	liver:	n/a	chr4:86747501-86747522
9	BHLHE40	chr4:86784052-86784326	K562	blood:	n/a	n/a
10	BHLHE40	chr4:86747365-86747701	A549	lung:	n/a	chr4:86747501-86747522
11	BHLHE40	chr4:86747358-86747692	GM12878	blood:	n/a	chr4:86747501-86747522
12	BHLHE40	chr4:86747332-86747692	K562	blood:	n/a	chr4:86747501-86747522
13	BHLHE40	chr4:86850104-86850271	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:86750600-86750697	A549	lung:	n/a	n/a
15	BHLHE40	chr4:86761532-86761752	K562	blood:	n/a	n/a
16	BRCA1	chr4:86811827-86811828	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:86763874-86763922	GM12878	blood:	n/a	n/a
18	CBX3	chr4:86874604-86875365	HCT-116	colon:	n/a	n/a
19	CCNT2	chr4:86876823-86877089	K562	blood:	n/a	n/a
20	CCNT2	chr4:86885400-86885546	K562	blood:	n/a	n/a
21	CEBPB	chr4:86874791-86875151	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:86893642-86893937	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:86873759-86874014	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:86748430-86748982	A549	lung:	n/a	chr4:86748482-86748493
25	CEBPB	chr4:86893716-86893924	K562	blood:	n/a	n/a
26	CEBPB	chr4:86860822-86861044	A549	lung:	n/a	chr4:86860966-86860977
27	CEBPB	chr4:86905811-86906054	IMR90	lung:	n/a	chr4:86905916-86905927
28	CEBPB	chr4:86853236-86853525	IMR90	lung:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
29	CEBPB	chr4:86873654-86874078	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:86802334-86802534	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:86874745-86875108	A549	lung:	n/a	n/a
32	CEBPB	chr4:86853257-86853549	A549	lung:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
33	CEBPB	chr4:86822659-86822977	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:86875043-86875049	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:86890193-86890453	A549	lung:	n/a	n/a
36	CEBPB	chr4:86878869-86879143	K562	blood:	n/a	n/a
37	CEBPB	chr4:86860830-86861051	HepG2	liver:	n/a	chr4:86860966-86860977
38	CEBPB	chr4:86874724-86875230	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:86853310-86853506	H1-hESC	embryonic stem cell:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
40	CEBPB	chr4:86854541-86854731	HepG2	liver:	n/a	chr4:86854570-86854581 chr4:86854569-86854582 chr4:86854569-86854582
41	CEBPB	chr4:86822575-86823018	A549	lung:	n/a	n/a
42	CEBPB	chr4:86890166-86890507	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:86748517-86748793	A549	lung:	n/a	n/a
44	CEBPB	chr4:86905831-86906042	HepG2	liver:	n/a	chr4:86905916-86905927
45	CEBPB	chr4:86907477-86907775	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:86748530-86748856	MCF-7	breast:	n/a	n/a
47	CEBPB	chr4:86874659-86875202	A549	lung:	n/a	n/a
48	CEBPB	chr4:86822635-86822935	A549	lung:	n/a	n/a
49	CEBPB	chr4:86890178-86890468	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:86831561-86831722	HepG2	liver:	n/a	chr4:86831593-86831604

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:86874205-86874255	HAEpiC	amniotic membrane:	n/a
2	chr4:86874205-86874255	HAEpiC	amniotic membrane:	n/a
3	chr4:86850721-86850771	HL-60	blood:	n/a
4	chr4:86851411-86851461	HRE	kidney:	n/a
5	chr4:86851425-86851475	IMR90	lung:	fetal
6	chr4:86851399-86851449	HCPEpiC	choroid plexus:	n/a
7	chr4:86852666-86852716	H1-hESC	embryonic stem cell:	embryo
8	chr4:86748949-86748999	HEK293	kidney:	embryo
9	chr4:86851425-86851475	SK-N-SH_RA	brain:	n/a
10	chr4:86850721-86850771	HCM	heart:	n/a
11	chr4:86749040-86749090	T-47D	breast:	n/a
12	chr4:86851225-86851275	GM12892	blood:	n/a
13	chr4:86748949-86748999	Hela-S3	cervix:	n/a
14	chr4:86851425-86851475	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:86851399-86851449	HEEpiC	esophagus:	n/a
16	chr4:86852666-86852716	MCF10A-Er-Src	breast:	n/a
17	chr4:86748949-86748999	T-47D	breast:	n/a
18	chr4:86748944-86748994	HIPEpiC	eye:	n/a
19	chr4:86874205-86874255	K562	blood:	n/a
20	chr4:86851425-86851475	HMEC	breast:	n/a
21	chr4:86851225-86851275	BE2_C	brain:	n/a
22	chr4:86850721-86850771	AG09319	gingival:	n/a
23	chr4:86745824-86745874	HRCEpiC	kidney:	n/a
24	chr4:86749040-86749090	HMEC	breast:	n/a
25	chr4:86749040-86749090	SK-N-SH	brain:	n/a
26	chr4:86850721-86850771	AG09309	skin:	n/a
27	chr4:86748944-86748994	NB4	blood:	n/a
28	chr4:86748949-86748999	RPTEC	kidney:	n/a
29	chr4:86748944-86748994	A549	lung:	n/a
30	chr4:86748944-86748994	H1-hESC	embryonic stem cell:	embryo
31	chr4:86852666-86852716	SAEC	small airway:	n/a
32	chr4:86745824-86745874	H1-hESC	embryonic stem cell:	embryo
33	chr4:86745824-86745874	Jurkat	blood:	n/a
34	chr4:86749040-86749090	HCPEpiC	choroid plexus:	n/a
35	chr4:86851425-86851475	Jurkat	blood:	n/a
36	chr4:86850721-86850771	GM12878	blood:	n/a
37	chr4:86874205-86874255	Jurkat	blood:	n/a
38	chr4:86749040-86749090	HAEpiC	amniotic membrane:	n/a
39	chr4:86874205-86874255	AG04450	lung:	fetal
40	chr4:86852666-86852716	PFSK-1	brain:	n/a
41	chr4:86852666-86852716	BJ	skin:	n/a
42	chr4:86851425-86851475	LNCaP	prostate:	n/a
43	chr4:86850721-86850771	SKMC	muscle:	n/a
44	chr4:86851399-86851449	HUVEC	blood vessel:	n/a
45	chr4:86851425-86851475	GM12891	blood:	n/a
46	chr4:86851411-86851461	HUVEC	blood vessel:	n/a
47	chr4:86851399-86851449	MCF-7	breast:	n/a
48	chr4:86748944-86748994	GM12878	blood:	n/a
49	chr4:86748944-86748994	Caco-2	colon:	n/a
50	chr4:86874205-86874255	Hepatocyte	liver:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:86851168..86853730-chr4:86855449..86857714,2	K562	blood:
2	chr4:86758093..86760173-chr4:86804562..86807184,2	MCF-7	breast:
3	chr4:86881196..86882931-chr4:86883765..86885876,2	K562	blood:
4	chr4:86855497..86859080-chr4:86873833..86876584,3	MCF-7	breast:
5	chr4:86678039..86678782-chr4:86890252..86890768,2	MCF-7	breast:
6	chr4:86717884..86718437-chr4:86885535..86886084,2	MCF-7	breast:
7	chr4:86858002..86860369-chr4:86861620..86863403,2	K562	blood:
8	chr4:86858002..86860369-chr4:86861620..86863403,2	K562	blood:
9	chr4:86717783..86718591-chr4:86885186..86885920,6	MCF-7	breast:
10	chr4:86829743..86832305-chr4:86837536..86839356,2	MCF-7	breast:
11	chr4:86855216..86857997-chr4:86860601..86862726,2	K562	blood:
12	chr4:86881196..86882931-chr4:86883765..86885876,2	K562	blood:
13	chr4:86747317..86749374-chr4:86754151..86756768,2	MCF-7	breast:
14	chr4:86853756..86855558-chr4:86856892..86859472,2	K562	blood:
15	chr4:86762784..86764294-chr4:86767286..86769112,2	MCF-7	breast:
16	chr4:86758093..86760173-chr4:86804562..86807184,2	MCF-7	breast:
17	chr4:86747130..86748178-chr4:86885197..86886140,3	MCF-7	breast:
18	chr4:86747130..86748178-chr4:86885197..86886140,3	MCF-7	breast:
19	chr4:86717774..86718537-chr4:86886876..86887427,3	MCF-7	breast:
20	chr4:86855216..86857997-chr4:86860601..86862726,2	K562	blood:
21	chr4:86855497..86859080-chr4:86873833..86876584,3	MCF-7	breast:
22	chr4:86853756..86855558-chr4:86856892..86859472,2	K562	blood:
23	chr4:86762784..86764294-chr4:86767286..86769112,2	MCF-7	breast:
24	chr4:86717537..86719169-chr4:86889518..86891294,13	MCF-7	breast:
25	chr4:86717573..86718676-chr4:86889897..86890637,3	MCF-7	breast:

No data

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: 5802 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:5802 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139990420	chr4:86745396-86745397	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs111236443	chr4:86745435-86745436	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs566691271	chr4:86745469-86745470	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs34242432	chr4:86745540-86745541	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs534136091	chr4:86745545-86745546	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs77488008	chr4:86745548-86745549	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs149849367	chr4:86745549-86745550	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs369902215	chr4:86745558-86745559	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs10016102	chr4:86745590-86745591	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs35702422	chr4:86745657-86745658	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs146676321	chr4:86745677-86745678	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs575423834	chr4:86745687-86745688	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs377466978	chr4:86745719-86745720	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs75183952	chr4:86745744-86745745	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs188958502	chr4:86745813-86745814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201267736	chr4:86745815-86745816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149921452	chr4:86745816-86745817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192732544	chr4:86745818-86745819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184707963	chr4:86745838-86745839	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs561764022	chr4:86745855-86745856	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs541049316	chr4:86745962-86745963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140223915	chr4:86746011-86746012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547223233	chr4:86746025-86746026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72658238	chr4:86746040-86746041	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs189178112	chr4:86746072-86746073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34622486	chr4:86746108-86746109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532806110	chr4:86746129-86746130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552012132	chr4:86746130-86746131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180873091	chr4:86746151-86746152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527878289	chr4:86746160-86746161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs67631333	chr4:86746244-86746245	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs559176239	chr4:86746250-86746251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79980676	chr4:86746256-86746257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201595083	chr4:86746265-86746266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79899426	chr4:86746266-86746267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146458928	chr4:86746268-86746269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367629779	chr4:86746270-86746271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370042017	chr4:86746271-86746272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149049291	chr4:86746365-86746366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574730788	chr4:86746371-86746372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374908046	chr4:86746403-86746404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189269470	chr4:86746438-86746439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79449143	chr4:86746482-86746483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573220533	chr4:86746484-86746485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34254172	chr4:86746515-86746516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559980409	chr4:86746523-86746524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533966109	chr4:86746617-86746618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555628777	chr4:86746618-86746619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576747460	chr4:86746628-86746629	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs181640028	chr4:86746651-86746652	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	20459617	CNVD

Chromatin state (count:2367 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86728200-86747200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:86729400-86747400	Weak transcription	Colon Smooth Muscle	Colon
3	chr4:86736200-86748600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr4:86737600-86763200	Weak transcription	Primary B cells from cord blood	blood
5	chr4:86740200-86747000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:86740200-86747200	Weak transcription	Fetal Lung	lung
7	chr4:86740200-86748600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:86740200-86748800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:86741600-86745800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr4:86741800-86747200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:86743000-86746000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:86743200-86745800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:86743200-86748800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:86743400-86745800	Enhancers	Osteobl	bone
15	chr4:86743600-86747200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:86743800-86747200	Weak transcription	Aorta	Aorta
17	chr4:86744200-86746000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:86744200-86748600	Enhancers	Fetal Heart	heart
19	chr4:86744200-86748600	Enhancers	HSMM	muscle
20	chr4:86744400-86745600	Flanking Active TSS	HUVEC	blood vessel
21	chr4:86744400-86746000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr4:86744400-86747000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr4:86744400-86747400	Enhancers	Fetal Kidney	kidney
24	chr4:86744600-86745600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr4:86744600-86745600	Enhancers	Rectal Smooth Muscle	rectum
26	chr4:86744600-86745800	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr4:86744600-86745800	Enhancers	Stomach Mucosa	stomach
28	chr4:86744600-86745800	Enhancers	HSMMtube	muscle
29	chr4:86744600-86746000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:86744600-86746000	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr4:86744600-86747000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:86744600-86748200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr4:86744600-86748600	Enhancers	Adipose Nuclei	Adipose
34	chr4:86744800-86745400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr4:86744800-86745600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr4:86744800-86745600	Active TSS	Stomach Smooth Muscle	stomach
37	chr4:86744800-86745800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:86744800-86746400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr4:86744800-86746400	Weak transcription	Fetal Intestine Small	intestine
40	chr4:86744800-86747200	Weak transcription	Spleen	Spleen
41	chr4:86744800-86747400	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr4:86744800-86747400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:86744800-86747400	Weak transcription	Brain Germinal Matrix	brain
44	chr4:86744800-86748600	Weak transcription	Pancreas	Pancrea
45	chr4:86745000-86745400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr4:86745000-86745400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:86745000-86745800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr4:86745000-86746400	Weak transcription	Fetal Muscle Leg	muscle
49	chr4:86745000-86747000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr4:86745000-86747200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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