Variant report

Variant	nsv879519
Chromosome Location	chr4:86786204-86871282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:213)
CpG islands
(count:367)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:213 , 50 per page) page: 1 2 3 4 5

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	BHLHE40	chr4:86850104-86850271	GM12878	blood:	n/a	n/a
3	BRCA1	chr4:86811827-86811828	GM12878	blood:	n/a	n/a
4	CEBPB	chr4:86822526-86823017	A549	lung:	n/a	n/a
5	CEBPB	chr4:86854541-86854731	HepG2	liver:	n/a	chr4:86854570-86854581 chr4:86854569-86854582 chr4:86854569-86854582
6	CEBPB	chr4:86822659-86822977	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:86853310-86853506	H1-hESC	embryonic stem cell:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
8	CEBPB	chr4:86853236-86853525	IMR90	lung:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
9	CEBPB	chr4:86802334-86802534	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:86860822-86861044	A549	lung:	n/a	chr4:86860966-86860977
11	CEBPB	chr4:86822575-86823018	A549	lung:	n/a	n/a
12	CEBPB	chr4:86822635-86822935	A549	lung:	n/a	n/a
13	CEBPB	chr4:86853257-86853549	A549	lung:	n/a	chr4:86853443-86853456 chr4:86853480-86853488
14	CEBPB	chr4:86860830-86861051	HepG2	liver:	n/a	chr4:86860966-86860977
15	CEBPB	chr4:86831561-86831722	HepG2	liver:	n/a	chr4:86831593-86831604
16	CHD1	chr4:86788492-86788586	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr4:86827044-86827063	GM13976	blood:	n/a	n/a
18	CTCF	chr4:86793820-86793970	GM12868	blood:	n/a	n/a
19	CTCF	chr4:86842925-86843019	Spleen_OC	spleen:	n/a	n/a
20	CTCF	chr4:86836769-86836853	GM13977	blood:	n/a	n/a
21	CTCF	chr4:86825120-86825270	AG09309	skin:	n/a	n/a
22	CTCF	chr4:86849663-86849690	GM10266	blood:	n/a	n/a
23	CTCF	chr4:86851060-86851210	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr4:86859460-86859610	Caco-2	colon:	n/a	n/a
25	CTCF	chr4:86850301-86850365	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr4:86798652-86798722	Lung_OC	lung:	n/a	n/a
27	CTCF	chr4:86842942-86843011	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr4:86831032-86831138	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr4:86849678-86849739	GM20000	blood:	n/a	n/a
30	E2F4	chr4:86850216-86850338	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr4:86830030-86830127	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr4:86845384-86845571	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr4:86789905-86790039	MCF10A-Er-Src	breast:	n/a	n/a
34	EP300	chr4:86850258-86850902	A549	lung:	n/a	n/a
35	EP300	chr4:86840064-86840162	GM12878	blood:	n/a	n/a
36	EP300	chr4:86822559-86823074	A549	lung:	n/a	n/a
37	FOS	chr4:86850083-86850090	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:86822727-86822863	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:86822632-86822923	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:86822673-86822912	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:86807755-86808528	HUVEC	blood vessel:	n/a	chr4:86808005-86808015 chr4:86808006-86808013 chr4:86808005-86808014 chr4:86807850-86807859 chr4:86808004-86808015 chr4:86808006-86808015
42	FOS	chr4:86822647-86822916	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:86807879-86808079	MCF10A-Er-Src	breast:	n/a	chr4:86808005-86808015 chr4:86808006-86808013 chr4:86808005-86808014 chr4:86808004-86808015 chr4:86808006-86808015
44	FOSL2	chr4:86807863-86808123	A549	lung:	n/a	chr4:86808005-86808015 chr4:86808006-86808013 chr4:86808005-86808014 chr4:86808006-86808015
45	FOXA1	chr4:86822647-86822986	T-47D	breast:	n/a	n/a
46	FOXA1	chr4:86791842-86792186	HepG2	liver:	n/a	n/a
47	FOXA1	chr4:86859316-86859620	HepG2	liver:	n/a	n/a
48	FOXA1	chr4:86822691-86823015	T-47D	breast:	n/a	n/a
49	FOXA2	chr4:86822639-86823004	A549	lung:	n/a	n/a
50	FOXA2	chr4:86816025-86816331	A549	lung:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:86850721-86850771	HepG2	liver:	n/a
2	chr4:86850721-86850771	HepG2	liver:	n/a
3	chr4:86850721-86850771	SAEC	small airway:	n/a
4	chr4:86851399-86851449	HEK293	kidney:	embryo
5	chr4:86851225-86851275	GM06990	blood:	n/a
6	chr4:86851225-86851275	Jurkat	blood:	n/a
7	chr4:86851399-86851449	SK-N-SH_RA	brain:	n/a
8	chr4:86852666-86852716	NHBE	bronchial:	n/a
9	chr4:86852666-86852716	BJ	skin:	n/a
10	chr4:86851411-86851461	PrEC	prostate:	n/a
11	chr4:86851225-86851275	NHBE	bronchial:	n/a
12	chr4:86851411-86851461	SAEC	small airway:	n/a
13	chr4:86851399-86851449	HNPCEpiC	eye:	n/a
14	chr4:86851399-86851449	GM12892	blood:	n/a
15	chr4:86852666-86852716	HepG2	liver:	n/a
16	chr4:86851411-86851461	CMK	blood:	n/a
17	chr4:86852666-86852716	PrEC	prostate:	n/a
18	chr4:86852666-86852716	HCF	heart:	n/a
19	chr4:86850721-86850771	LNCaP	prostate:	n/a
20	chr4:86852666-86852716	HEK293	kidney:	embryo
21	chr4:86852666-86852716	AG09309	skin:	n/a
22	chr4:86851411-86851461	GM06990	blood:	n/a
23	chr4:86851225-86851275	IMR90	lung:	fetal
24	chr4:86851411-86851461	GM12878	blood:	n/a
25	chr4:86851411-86851461	ProgFib	skin:	n/a
26	chr4:86851225-86851275	GM12892	blood:	n/a
27	chr4:86850721-86850771	CMK	blood:	n/a
28	chr4:86851425-86851475	Caco-2	colon:	n/a
29	chr4:86852666-86852716	ovcar-3	ovarian:	n/a
30	chr4:86852666-86852716	NH-A	brain:	n/a
31	chr4:86851399-86851449	GM06990	blood:	n/a
32	chr4:86851225-86851275	HCF	heart:	n/a
33	chr4:86851399-86851449	BJ	skin:	n/a
34	chr4:86851399-86851449	HIPEpiC	eye:	n/a
35	chr4:86851425-86851475	HUVEC	blood vessel:	n/a
36	chr4:86850721-86850771	HNPCEpiC	eye:	n/a
37	chr4:86852666-86852716	SK-N-SH	brain:	n/a
38	chr4:86851399-86851449	NH-A	brain:	n/a
39	chr4:86851425-86851475	BJ	skin:	n/a
40	chr4:86852666-86852716	GM12878	blood:	n/a
41	chr4:86851425-86851475	HAEpiC	amniotic membrane:	n/a
42	chr4:86852666-86852716	MCF-7	breast:	n/a
43	chr4:86851411-86851461	HMEC	breast:	n/a
44	chr4:86851425-86851475	A549	lung:	n/a
45	chr4:86851225-86851275	ProgFib	skin:	n/a
46	chr4:86851399-86851449	ProgFib	skin:	n/a
47	chr4:86852666-86852716	U87	brain:	n/a
48	chr4:86852666-86852716	SK-N-MC	brain:	n/a
49	chr4:86851225-86851275	U87	brain:	n/a
50	chr4:86851425-86851475	HCT-116	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:86853756..86855558-chr4:86856892..86859472,2	K562	blood:
2	chr4:86855216..86857997-chr4:86860601..86862726,2	K562	blood:
3	chr4:86758093..86760173-chr4:86804562..86807184,2	MCF-7	breast:
4	chr4:86829743..86832305-chr4:86837536..86839356,2	MCF-7	breast:
5	chr4:86855216..86857997-chr4:86860601..86862726,2	K562	blood:
6	chr4:86858002..86860369-chr4:86861620..86863403,2	K562	blood:
7	chr4:86855497..86859080-chr4:86873833..86876584,3	MCF-7	breast:
8	chr4:86858002..86860369-chr4:86861620..86863403,2	K562	blood:
9	chr4:86853756..86855558-chr4:86856892..86859472,2	K562	blood:
10	chr4:86851168..86853730-chr4:86855449..86857714,2	K562	blood:

No data

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

Extended variants
information (count: 3032 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:3032 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs345349	chr4:86786204-86786205	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35877758	chr4:86786306-86786307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181811192	chr4:86786331-86786332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139626022	chr4:86786379-86786380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574158298	chr4:86786456-86786457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528978450	chr4:86786474-86786475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs345348	chr4:86786509-86786510	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs76930533	chr4:86786568-86786569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558820583	chr4:86786604-86786605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs345347	chr4:86786634-86786635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541171850	chr4:86786702-86786703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs345346	chr4:86786756-86786757	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567031804	chr4:86786757-86786758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs345345	chr4:86786778-86786779	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374790121	chr4:86786866-86786867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375583479	chr4:86786890-86786891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555939916	chr4:86786898-86786899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567732373	chr4:86786938-86786939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114656054	chr4:86787082-86787083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs345344	chr4:86787083-86787084	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs578106322	chr4:86787096-86787097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186495966	chr4:86787107-86787108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553391630	chr4:86787122-86787123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs345343	chr4:86787123-86787124	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573108022	chr4:86787241-86787242	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115077412	chr4:86787284-86787285	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs528770683	chr4:86787290-86787291	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs561548778	chr4:86787390-86787391	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs528915842	chr4:86787408-86787409	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543942091	chr4:86787421-86787422	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562139935	chr4:86787432-86787433	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532792080	chr4:86787454-86787455	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552034873	chr4:86787457-86787458	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573318683	chr4:86787486-86787487	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528008347	chr4:86787489-86787490	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549261626	chr4:86787526-86787527	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567867406	chr4:86787557-86787558	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145015286	chr4:86787594-86787595	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556726108	chr4:86787698-86787699	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191348454	chr4:86787708-86787709	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs6843333	chr4:86787721-86787722	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs554160020	chr4:86787791-86787792	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573008274	chr4:86787831-86787832	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13134118	chr4:86787860-86787861	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs555132756	chr4:86787863-86787864	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573545468	chr4:86787866-86787867	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368765386	chr4:86787950-86787951	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149090927	chr4:86787990-86787991	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577680413	chr4:86787991-86787992	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371764724	chr4:86788011-86788012	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86749400-86787600	Weak transcription	Pancreas	Pancrea
2	chr4:86750000-86809200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr4:86776000-86790400	Weak transcription	Right Atrium	heart
4	chr4:86779800-86800200	Weak transcription	Primary B cells from cord blood	blood
5	chr4:86780400-86787600	Weak transcription	Colon Smooth Muscle	Colon
6	chr4:86780400-86790800	Weak transcription	Gastric	stomach
7	chr4:86781400-86787400	Weak transcription	HSMM	muscle
8	chr4:86781600-86787600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr4:86781800-86787200	Weak transcription	HSMMtube	muscle
10	chr4:86781800-86787400	Weak transcription	Fetal Muscle Leg	muscle
11	chr4:86781800-86787400	Enhancers	NHDF-Ad	bronchial
12	chr4:86781800-86787600	Weak transcription	NHLF	lung
13	chr4:86781800-86787800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr4:86781800-86789000	Weak transcription	Small Intestine	intestine
15	chr4:86781800-86790400	Weak transcription	NH-A	brain
16	chr4:86782000-86787000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:86782400-86788400	Weak transcription	Stomach Smooth Muscle	stomach
18	chr4:86782600-86787400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:86782600-86787400	Weak transcription	Aorta	Aorta
20	chr4:86782600-86787600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr4:86782800-86787000	Weak transcription	Osteobl	bone
22	chr4:86782800-86791600	Weak transcription	Duodenum Mucosa	Duodenum
23	chr4:86783000-86787000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr4:86783200-86786600	Weak transcription	Fetal Brain Male	brain
25	chr4:86783200-86787200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr4:86783400-86787600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr4:86783400-86787600	Weak transcription	Fetal Stomach	stomach
28	chr4:86783600-86787200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:86783600-86788400	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr4:86784000-86790200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr4:86784200-86789400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr4:86785200-86786400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr4:86785400-86786400	Enhancers	HUVEC	blood vessel
34	chr4:86785400-86787200	Weak transcription	Fetal Kidney	kidney
35	chr4:86785800-86787600	Weak transcription	Stomach Mucosa	stomach
36	chr4:86786000-86786600	Enhancers	Liver	Liver
37	chr4:86786000-86787600	Weak transcription	Primary B cells from peripheral blood	blood
38	chr4:86786200-86786400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:86786200-86786400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr4:86786400-86786800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:86786400-86787000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr4:86786400-86787400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:86786400-86787400	Weak transcription	HUVEC	blood vessel
44	chr4:86786600-86787600	Weak transcription	Liver	Liver
45	chr4:86786800-86787800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr4:86787000-86787200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr4:86787000-86787400	Enhancers	Osteobl	bone
48	chr4:86787000-86787600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:86787000-86788000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr4:86787200-86787400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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