Variant report

Variant	esv1795614
Chromosome Location	chr4:160142544-160161916
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:315)
CpG islands
(count:62)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:160157192-160157387	K562	blood:	n/a	n/a
2	BACH1	chr4:160150350-160150633	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:160161838-160162180	K562	blood:	n/a	n/a
4	BCL11A	chr4:160153923-160154079	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:160148646-160148928	K562	blood:	n/a	n/a
6	BHLHE40	chr4:160159220-160159412	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:160146777-160147059	K562	blood:	n/a	n/a
8	BRCA1	chr4:160149126-160149708	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:160145571-160145892	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:160161736-160162028	K562	blood:	n/a	n/a
11	CEBPB	chr4:160161720-160162051	HepG2	liver:	n/a	chr4:160162024-160162036
12	CEBPB	chr4:160149041-160149446	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:160161739-160162062	H1-hESC	embryonic stem cell:	n/a	chr4:160162024-160162036
14	CEBPB	chr4:160161702-160162124	IMR90	lung:	n/a	chr4:160162024-160162036
15	CEBPB	chr4:160161818-160162057	A549	lung:	n/a	chr4:160162024-160162036
16	CEBPB	chr4:160150254-160150757	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:160161735-160162105	Hela-S3	cervix:	n/a	chr4:160162024-160162036
18	CEBPB	chr4:160147803-160148083	K562	blood:	n/a	chr4:160147937-160147950
19	CEBPB	chr4:160161732-160162014	ECC-1	luminal epithelium:	n/a	n/a
20	CHD2	chr4:160149185-160149544	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr4:160150528-160150563	HepG2	liver:	n/a	n/a
22	CTCF	chr4:160149280-160149430	BJ	skin:	n/a	n/a
23	CTCF	chr4:160149220-160149370	HCM	heart:	n/a	n/a
24	CTCF	chr4:160149220-160149370	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr4:160149260-160149410	HMEC	breast:	n/a	n/a
26	CTCF	chr4:160149200-160149350	HEK293	kidney:	n/a	n/a
27	CTCF	chr4:160149240-160149390	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr4:160149240-160149390	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr4:160149180-160149330	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr4:160149200-160149350	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr4:160149280-160149430	HCT-116	colon:	n/a	n/a
32	CTCF	chr4:160149160-160149310	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr4:160159033-160159125	ProgFib	skin:	n/a	n/a
34	CTCF	chr4:160149220-160149370	HFF	foreskin:	n/a	n/a
35	CTCF	chr4:160149220-160149370	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr4:160149220-160149370	AG04449	skin:	n/a	n/a
37	CTCF	chr4:160149220-160149370	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr4:160149240-160149390	AG09319	gingival:	n/a	n/a
39	CTCF	chr4:160149240-160149390	HMEC	breast:	n/a	n/a
40	CTCF	chr4:160149280-160149430	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr4:160149220-160149370	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr4:160149160-160149310	NHLF	lung:	n/a	n/a
43	CTCF	chr4:160149260-160149410	HVMF	connective:	n/a	n/a
44	CTCF	chr4:160149300-160149450	AG04450	lung:	n/a	n/a
45	CTCF	chr4:160149200-160149350	HRE	kidney:	n/a	n/a
46	CTCF	chr4:160149260-160149410	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr4:160149240-160149390	SAEC	small airway:	n/a	n/a
48	CTCF	chr4:160149220-160149370	AG09309	skin:	n/a	n/a
49	CTCF	chr4:160149220-160149370	WI-38	lung:	n/a	n/a
50	CTCF	chr4:160149220-160149370	NHEK	skin:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:160149604-160149654	AG10803	skin:	n/a
2	chr4:160149604-160149654	AG10803	skin:	n/a
3	chr4:160149604-160149654	HMEC	breast:	n/a
4	chr4:160149604-160149654	U87	brain:	n/a
5	chr4:160149604-160149654	SK-N-SH_RA	brain:	n/a
6	chr4:160149604-160149654	GM19239	blood:	n/a
7	chr4:160149604-160149654	AG09309	skin:	n/a
8	chr4:160149604-160149654	SKMC	muscle:	n/a
9	chr4:160149604-160149654	HEK293	kidney:	embryo
10	chr4:160149604-160149654	CMK	blood:	n/a
11	chr4:160149604-160149654	ECC-1	luminal epithelium:	n/a
12	chr4:160149604-160149654	HCT-116	colon:	n/a
13	chr4:160149604-160149654	NHBE	bronchial:	n/a
14	chr4:160149604-160149654	PrEC	prostate:	n/a
15	chr4:160149604-160149654	GM12878	blood:	n/a
16	chr4:160149604-160149654	Caco-2	colon:	n/a
17	chr4:160149604-160149654	RPTEC	kidney:	n/a
18	chr4:160149604-160149654	HEEpiC	esophagus:	n/a
19	chr4:160149604-160149654	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:160149604-160149654	T-47D	breast:	n/a
21	chr4:160149604-160149654	AoSMC	blood vessel:	n/a
22	chr4:160149604-160149654	AG04450	lung:	fetal
23	chr4:160149604-160149654	PFSK-1	brain:	n/a
24	chr4:160149604-160149654	Jurkat	blood:	n/a
25	chr4:160149604-160149654	HRE	kidney:	n/a
26	chr4:160149604-160149654	A549	lung:	n/a
27	chr4:160149604-160149654	NHDF-neo	bronchial:	n/a
28	chr4:160149604-160149654	GM12891	blood:	n/a
29	chr4:160149604-160149654	MCF-7	breast:	n/a
30	chr4:160149604-160149654	HCF	heart:	n/a
31	chr4:160149604-160149654	PANC-1	pancreas:	n/a
32	chr4:160149604-160149654	Hela-S3	cervix:	n/a
33	chr4:160149604-160149654	Hepatocyte	liver:	n/a
34	chr4:160149604-160149654	AG09319	gingival:	n/a
35	chr4:160149604-160149654	HAEpiC	amniotic membrane:	n/a
36	chr4:160149604-160149654	IMR90	lung:	fetal
37	chr4:160149604-160149654	HIPEpiC	eye:	n/a
38	chr4:160149604-160149654	BJ	skin:	n/a
39	chr4:160149604-160149654	HCM	heart:	n/a
40	chr4:160149604-160149654	LNCaP	prostate:	n/a
41	chr4:160149604-160149654	ProgFib	skin:	n/a
42	chr4:160149604-160149654	H1-hESC	embryonic stem cell:	embryo
43	chr4:160149604-160149654	HUVEC	blood vessel:	n/a
44	chr4:160149604-160149654	NB4	blood:	n/a
45	chr4:160149604-160149654	HL-60	blood:	n/a
46	chr4:160149604-160149654	NH-A	brain:	n/a
47	chr4:160149604-160149654	HRCEpiC	kidney:	n/a
48	chr4:160149604-160149654	HNPCEpiC	eye:	n/a
49	chr4:160149604-160149654	GM12892	blood:	n/a
50	chr4:160149604-160149654	HCPEpiC	choroid plexus:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:160139791..160142623-chr4:160144454..160146508,3	K562	blood:
2	chr4:160144300..160148561-chr4:160148717..160151387,4	MCF-7	breast:
3	chr4:160139791..160142623-chr4:160144454..160146508,3	K562	blood:

No data

Variant related genes	Relation type
RAPGEF2	TF binding region
RAPGEF2	CpG island
ENSG00000109756	chromatin interactions

Extended variants
information (count: 652 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186557010	chr4:160142587-160142588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78832490	chr4:160142610-160142611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566833035	chr4:160142637-160142638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371776129	chr4:160142638-160142639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568393703	chr4:160142646-160142647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73859104	chr4:160142650-160142651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs547653388	chr4:160142678-160142679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191005559	chr4:160142708-160142709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539675100	chr4:160142725-160142726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556715507	chr4:160142752-160142753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575286127	chr4:160142773-160142774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537906998	chr4:160142774-160142775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554271398	chr4:160142787-160142788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4691547	chr4:160142858-160142859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs72699342	chr4:160142860-160142861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs59855612	chr4:160142863-160142864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183727030	chr4:160142919-160142920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188498079	chr4:160142945-160142946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150901557	chr4:160142947-160142948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370691502	chr4:160142977-160142978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13131413	chr4:160143026-160143027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531713605	chr4:160143060-160143061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542277889	chr4:160143067-160143068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561957429	chr4:160143074-160143075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190449113	chr4:160143100-160143101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547366963	chr4:160143151-160143152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570859443	chr4:160143158-160143159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375258004	chr4:160143175-160143176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550118370	chr4:160143184-160143185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376342488	chr4:160143231-160143232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570185212	chr4:160143239-160143240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138297037	chr4:160143269-160143270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554683379	chr4:160143294-160143295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568139328	chr4:160143322-160143323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183432067	chr4:160143345-160143346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370690020	chr4:160143392-160143393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147776820	chr4:160143410-160143411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142932374	chr4:160143444-160143445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187755199	chr4:160143452-160143453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546028715	chr4:160143454-160143455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556104697	chr4:160143522-160143523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191298004	chr4:160143578-160143579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553018135	chr4:160143586-160143587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12502799	chr4:160143615-160143616	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs34947842	chr4:160143617-160143618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184145471	chr4:160143651-160143652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112723660	chr4:160143657-160143658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373697300	chr4:160143666-160143667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111354583	chr4:160143679-160143680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544780047	chr4:160143691-160143692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19805367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160097400-160143200	Weak transcription	Fetal Intestine Large	intestine
2	chr4:160101400-160143400	Weak transcription	Fetal Kidney	kidney
3	chr4:160102000-160149000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:160107000-160145600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr4:160115600-160149200	Weak transcription	Esophagus	oesophagus
6	chr4:160116600-160145200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr4:160116800-160148200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:160119000-160148600	Weak transcription	Small Intestine	intestine
9	chr4:160125200-160148600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr4:160126600-160142800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr4:160127800-160148600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr4:160128000-160148600	Weak transcription	NHDF-Ad	bronchial
13	chr4:160128400-160148600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:160128600-160148400	Weak transcription	Stomach Mucosa	stomach
15	chr4:160129200-160148200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr4:160130800-160148600	Weak transcription	Ovary	ovary
17	chr4:160132400-160148600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:160132400-160148600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:160132400-160149200	Weak transcription	Brain Germinal Matrix	brain
20	chr4:160132800-160148000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:160133400-160143200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:160133400-160171600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr4:160134200-160156600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:160135600-160142800	Weak transcription	Brain Substantia Nigra	brain
25	chr4:160136600-160143200	Weak transcription	Fetal Intestine Small	intestine
26	chr4:160138000-160145400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr4:160138000-160156000	Weak transcription	Primary hematopoietic stem cells	blood
28	chr4:160138200-160142600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:160138200-160142800	Weak transcription	Brain Anterior Caudate	brain
30	chr4:160138600-160142600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:160138800-160148600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr4:160139000-160142800	Weak transcription	Fetal Brain Female	brain
33	chr4:160139600-160142800	Weak transcription	Colon Smooth Muscle	Colon
34	chr4:160140800-160144000	Enhancers	Fetal Heart	heart
35	chr4:160141000-160143800	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr4:160141200-160142600	Enhancers	Psoas Muscle	Psoas
37	chr4:160141200-160145600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:160141400-160142600	Enhancers	Left Ventricle	heart
39	chr4:160141400-160144800	Weak transcription	Liver	Liver
40	chr4:160141400-160145200	Weak transcription	HepG2	liver
41	chr4:160141400-160145400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr4:160141400-160148600	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr4:160141400-160148800	Weak transcription	Fetal Muscle Leg	muscle
44	chr4:160141800-160143400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr4:160141800-160148600	Weak transcription	Pancreas	Pancrea
46	chr4:160142000-160143600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr4:160142200-160142600	Enhancers	Right Ventricle	heart
48	chr4:160142200-160143000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:160142200-160143600	Enhancers	Right Atrium	heart
50	chr4:160142200-160144000	Enhancers	Brain Angular Gyrus	brain

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