Variant report

Variant	nsv997304
Chromosome Location	chr4:96575198-96861349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:829)
CpG islands
(count:798)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:96614804-96615129	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:96614717-96615069	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:96756891-96757056	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr4:96720028-96720203	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr4:96720077-96720233	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr4:96603085-96603089	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr4:96833916-96833938	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr4:96847445-96847700	K562	blood:	n/a	n/a
9	CBX3	chr4:96789054-96789386	K562	blood:	n/a	n/a
10	CBX3	chr4:96789068-96789369	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:96789036-96789470	HCT-116	colon:	n/a	n/a
12	CEBPB	chr4:96693254-96693466	HepG2	liver:	n/a	chr4:96693362-96693373
13	CEBPB	chr4:96636962-96637451	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr4:96845178-96845472	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:96791240-96791451	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:96693229-96693518	IMR90	lung:	n/a	chr4:96693362-96693373
17	CEBPB	chr4:96809307-96809514	HepG2	liver:	n/a	chr4:96809374-96809385
18	CEBPB	chr4:96719923-96720273	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:96668490-96669010	MCF-7	breast:	n/a	n/a
20	CEBPB	chr4:96702036-96702236	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:96702017-96702218	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:96597442-96597596	H1-hESC	embryonic stem cell:	n/a	chr4:96597565-96597576
23	CEBPB	chr4:96649198-96649434	HepG2	liver:	n/a	chr4:96649277-96649288 chr4:96649328-96649339
24	CEBPB	chr4:96636884-96637398	MCF-7	breast:	n/a	n/a
25	CEBPB	chr4:96597442-96597710	IMR90	lung:	n/a	chr4:96597565-96597576
26	CEBPB	chr4:96703580-96703990	A549	lung:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
27	CEBPB	chr4:96597411-96597724	HepG2	liver:	n/a	chr4:96597565-96597576
28	CEBPB	chr4:96703619-96704039	IMR90	lung:	n/a	chr4:96703699-96703710 chr4:96703701-96703710 chr4:96704005-96704016
29	CEBPB	chr4:96649188-96649501	A549	lung:	n/a	chr4:96649277-96649288 chr4:96649328-96649339
30	CEBPB	chr4:96597434-96597706	A549	lung:	n/a	chr4:96597565-96597576
31	CEBPB	chr4:96578513-96578622	A549	lung:	n/a	n/a
32	CEBPB	chr4:96703666-96703970	HepG2	liver:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
33	CEBPB	chr4:96578583-96578682	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:96702003-96702220	A549	lung:	n/a	n/a
35	CEBPB	chr4:96809244-96809518	IMR90	lung:	n/a	chr4:96809374-96809385
36	CEBPB	chr4:96653308-96653672	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr4:96703659-96703859	K562	blood:	n/a	chr4:96703699-96703710 chr4:96703701-96703710
38	CEBPB	chr4:96636890-96637488	MCF-7	breast:	n/a	n/a
39	CEBPB	chr4:96668531-96669056	MCF-7	breast:	n/a	chr4:96669001-96669014
40	CEBPB	chr4:96781173-96781373	HepG2	liver:	n/a	chr4:96781272-96781281 chr4:96781270-96781281 chr4:96781272-96781281 chr4:96781270-96781283 chr4:96781270-96781283 chr4:96781272-96781281 chr4:96781272-96781281 chr4:96781272-96781283 chr4:96781272-96781283
41	CEBPB	chr4:96637023-96637373	ECC-1	luminal epithelium:	n/a	n/a
42	CHD1	chr4:96723453-96723459	GM12878	blood:	n/a	n/a
43	CHD1	chr4:96719677-96719682	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr4:96719273-96719276	GM12878	blood:	n/a	n/a
45	CTCF	chr4:96756784-96757181	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:96756960-96757110	GM12873	blood:	n/a	n/a
47	CTCF	chr4:96614820-96614970	AG04450	lung:	n/a	n/a
48	CTCF	chr4:96756875-96757100	K562	blood:	n/a	n/a
49	CTCF	chr4:96756925-96757120	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:96756960-96757110	GM12878	blood:	n/a	n/a

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:96761559-96761609	HMEC	breast:	n/a
2	chr4:96761377-96761427	HEEpiC	esophagus:	n/a
3	chr4:96761135-96761185	GM06990	blood:	n/a
4	chr4:96760945-96760995	BJ	skin:	n/a
5	chr4:96761598-96761648	HL-60	blood:	n/a
6	chr4:96761559-96761609	HMEC	breast:	n/a
7	chr4:96761377-96761427	HEEpiC	esophagus:	n/a
8	chr4:96761135-96761185	GM06990	blood:	n/a
9	chr4:96760945-96760995	BJ	skin:	n/a
10	chr4:96761598-96761648	HL-60	blood:	n/a
11	chr4:96761135-96761185	MCF-7	breast:	n/a
12	chr4:96761377-96761427	HRE	kidney:	n/a
13	chr4:96760945-96760995	Jurkat	blood:	n/a
14	chr4:96761135-96761185	SK-N-MC	brain:	n/a
15	chr4:96761796-96761846	Jurkat	blood:	n/a
16	chr4:96761796-96761846	SK-N-SH	brain:	n/a
17	chr4:96761264-96761314	ProgFib	skin:	n/a
18	chr4:96760014-96760064	NH-A	brain:	n/a
19	chr4:96761264-96761314	AG10803	skin:	n/a
20	chr4:96761026-96761076	HMEC	breast:	n/a
21	chr4:96678053-96678103	SKMC	muscle:	n/a
22	chr4:96760945-96760995	RPTEC	kidney:	n/a
23	chr4:96761377-96761427	HCF	heart:	n/a
24	chr4:96761559-96761609	HUVEC	blood vessel:	n/a
25	chr4:96761377-96761427	HRPEpiC	eye:	n/a
26	chr4:96761559-96761609	Hepatocyte	liver:	n/a
27	chr4:96760014-96760064	BJ	skin:	n/a
28	chr4:96761231-96761281	HCM	heart:	n/a
29	chr4:96761264-96761314	IMR90	lung:	fetal
30	chr4:96761598-96761648	RPTEC	kidney:	n/a
31	chr4:96761135-96761185	HepG2	liver:	n/a
32	chr4:96761264-96761314	AG04449	skin:	fetal
33	chr4:96836082-96836132	AG09309	skin:	n/a
34	chr4:96760014-96760064	HNPCEpiC	eye:	n/a
35	chr4:96761231-96761281	AG09309	skin:	n/a
36	chr4:96761264-96761314	AoSMC	blood vessel:	n/a
37	chr4:96761559-96761609	NHDF-neo	bronchial:	n/a
38	chr4:96761264-96761314	HRE	kidney:	n/a
39	chr4:96678053-96678103	PANC-1	pancreas:	n/a
40	chr4:96761377-96761427	NT2-D1	testis:	n/a
41	chr4:96761264-96761314	NH-A	brain:	n/a
42	chr4:96761026-96761076	HCPEpiC	choroid plexus:	n/a
43	chr4:96761559-96761609	MCF10A-Er-Src	breast:	n/a
44	chr4:96761231-96761281	LNCaP	prostate:	n/a
45	chr4:96761377-96761427	GM12892	blood:	n/a
46	chr4:96761229-96761279	A549	lung:	n/a
47	chr4:96678053-96678103	HIPEpiC	eye:	n/a
48	chr4:96761377-96761427	HUVEC	blood vessel:	n/a
49	chr4:96678053-96678103	PFSK-1	brain:	n/a
50	chr4:96761598-96761648	Hela-S3	cervix:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:96669276..96670825-chr4:96677264..96679662,2	MCF-7	breast:
2	chr1:149223221..149225022-chr4:96577789..96580768,2	MCF-7	breast:
3	chr4:96674646..96677370-chr4:96678560..96681527,2	MCF-7	breast:
4	chr4:96817765..96820012-chr4:96825569..96827518,2	K562	blood:
5	chr4:96720160..96722789-chr4:96726350..96727999,2	K562	blood:
6	chr4:96674646..96677370-chr4:96678560..96681527,2	MCF-7	breast:
7	chr4:96822970..96824843-chr4:96830954..96833894,2	K562	blood:
8	chr4:96749923..96752182-chr4:96773061..96775566,2	K562	blood:
9	chr4:96720160..96722789-chr4:96726350..96727999,2	K562	blood:
10	chr4:96669276..96670825-chr4:96677264..96679662,2	MCF-7	breast:
11	chr4:96749923..96752182-chr4:96773061..96775566,2	K562	blood:
12	chr4:96614781..96615424-chr4:97273090..97273698,2	MCF-7	breast:
13	chr4:96817765..96820012-chr4:96825569..96827518,2	K562	blood:
14	chr4:96756581..96757503-chr4:96956588..96957342,2	MCF-7	breast:
15	chr4:96822970..96824843-chr4:96830954..96833894,2	K562	blood:

No data

Variant related genes	Relation type
PDHA2	TF binding region
RNU6-1059P	TF binding region
PDHA2	CpG island
RNU6-1059P	CpG island
ENSG00000206737	chromatin interactions

Extended variants
information (count: 6067 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6067 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76083532	chr4:96575200-96575201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533912781	chr4:96575279-96575280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142770355	chr4:96575281-96575282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188857326	chr4:96575376-96575377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550725940	chr4:96575381-96575382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569329180	chr4:96575383-96575384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539583212	chr4:96575389-96575390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540643566	chr4:96575414-96575415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114267337	chr4:96575431-96575432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114861471	chr4:96575507-96575508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115317019	chr4:96575530-96575531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201867577	chr4:96575555-96575556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7658020	chr4:96577810-96577811	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs140318191	chr4:96577831-96577832	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568229662	chr4:96577857-96577858	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs75001780	chr4:96577866-96577867	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs114171245	chr4:96577903-96577904	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs570606535	chr4:96577948-96577949	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368803552	chr4:96578046-96578047	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113175333	chr4:96578047-96578048	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142103276	chr4:96578061-96578062	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs151178798	chr4:96578078-96578079	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190222921	chr4:96578103-96578104	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373093499	chr4:96578154-96578155	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs10024465	chr4:96578160-96578161	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs149838266	chr4:96578208-96578209	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115494969	chr4:96578209-96578210	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs62307201	chr4:96578223-96578224	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs545813567	chr4:96578289-96578290	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559299773	chr4:96578290-96578291	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576868807	chr4:96578316-96578317	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546123603	chr4:96578322-96578323	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140696760	chr4:96578353-96578354	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs542298316	chr4:96578367-96578368	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs76781852	chr4:96578423-96578424	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200364047	chr4:96578428-96578429	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs546764971	chr4:96578438-96578439	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs34147144	chr4:96578445-96578446	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530733836	chr4:96578471-96578472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377738067	chr4:96578570-96578571	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550459344	chr4:96578585-96578586	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144526334	chr4:96578594-96578595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372333870	chr4:96578642-96578643	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533238037	chr4:96578645-96578646	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs116052008	chr4:96578665-96578666	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182576717	chr4:96578685-96578686	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs114851740	chr4:96578730-96578731	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549059968	chr4:96578736-96578737	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs138650485	chr4:96578739-96578740	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs141251574	chr4:96578757-96578758	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Lung cancer	18438408	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
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96575200-96575600	Enhancers	HUVEC	blood vessel
2	chr4:96581800-96582600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:96582000-96582400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:96582000-96582600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr4:96593600-96597800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:96594000-96596800	Enhancers	Fetal Kidney	kidney
7	chr4:96594200-96594400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr4:96594200-96594600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:96594200-96596800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:96594400-96595000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr4:96594600-96595000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:96594600-96596400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:96595000-96595800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr4:96595000-96597000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:96595400-96595800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:96595400-96596000	Enhancers	Fetal Lung	lung
17	chr4:96595600-96596400	Enhancers	Ovary	ovary
18	chr4:96595800-96596200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:96595800-96597000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:96597000-96597600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr4:96597400-96597800	Enhancers	HSMM	muscle
22	chr4:96602200-96604200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr4:96602800-96603400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:96602800-96603400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr4:96610600-96610800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:96610600-96611000	Enhancers	Right Atrium	heart
27	chr4:96613000-96613600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:96615000-96616800	Enhancers	HUVEC	blood vessel
29	chr4:96616800-96622200	Weak transcription	HUVEC	blood vessel
30	chr4:96617800-96618400	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr4:96618400-96618800	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr4:96619200-96620800	Enhancers	Dnd41	blood
33	chr4:96621000-96622600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:96622000-96622400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
35	chr4:96622200-96622400	Enhancers	Ovary	ovary
36	chr4:96622200-96622600	Enhancers	HSMMtube	muscle
37	chr4:96622200-96623600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:96622200-96623600	Enhancers	HUVEC	blood vessel
39	chr4:96622400-96622600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr4:96622400-96623400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:96622400-96623600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:96622400-96623600	Enhancers	HSMM	muscle
43	chr4:96622600-96622800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:96622600-96623200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:96622600-96623600	Enhancers	HMEC	breast
46	chr4:96622600-96623800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:96622800-96623200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr4:96622800-96623200	Enhancers	NH-A	brain
49	chr4:96622800-96623400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:96622800-96623400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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