Variant report

Variant	nsv593449
Chromosome Location	chr4:3342954-3346617
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:184)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3344203-3344571	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:3344062-3344569	HepG2	liver:	n/a	n/a
3	BHLHE40	chr4:3344223-3344438	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:3344231-3344498	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:3344175-3344470	HepG2	liver:	n/a	n/a
6	BHLHE40	chr4:3344140-3344381	K562	blood:	n/a	n/a
7	BHLHE40	chr4:3344203-3344494	A549	lung:	n/a	n/a
8	CTCF	chr4:3346420-3346570	GM12866	blood:	n/a	chr4:3346457-3346466
9	CTCF	chr4:3342840-3342990	HRE	kidney:	n/a	n/a
10	ELK1	chr4:3343723-3343729	Hela-S3	cervix:	n/a	n/a
11	EP300	chr4:3344222-3344605	HepG2	liver:	n/a	n/a
12	FOS	chr4:3343941-3344661	HUVEC	blood vessel:	n/a	n/a
13	FOSL2	chr4:3344071-3344578	A549	lung:	n/a	n/a
14	FOSL2	chr4:3344139-3344500	HepG2	liver:	n/a	n/a
15	FOXA1	chr4:3344031-3344687	HepG2	liver:	n/a	n/a
16	FOXA1	chr4:3344176-3344570	HepG2	liver:	n/a	n/a
17	FOXA1	chr4:3344103-3344602	HepG2	liver:	n/a	n/a
18	FOXA1	chr4:3344038-3344649	HepG2	liver:	n/a	n/a
19	FOXA2	chr4:3344153-3344575	A549	lung:	n/a	n/a
20	FOXA2	chr4:3343919-3344849	HepG2	liver:	n/a	n/a
21	FOXA2	chr4:3344063-3344647	A549	lung:	n/a	n/a
22	FOXA2	chr4:3344177-3344501	HepG2	liver:	n/a	n/a
23	GATA2	chr4:3343722-3344400	HUVEC	blood vessel:	n/a	chr4:3344102-3344112
24	HNF4A	chr4:3344170-3344454	HepG2	liver:	n/a	n/a
25	IRF3	chr4:3344266-3344324	GM12878	blood:	n/a	n/a
26	JUN	chr4:3344185-3344544	HepG2	liver:	n/a	n/a
27	JUND	chr4:3344199-3344486	HepG2	liver:	n/a	n/a
28	JUND	chr4:3344185-3344508	HepG2	liver:	n/a	n/a
29	KAP1	chr4:3344116-3344586	HEK293	kidney:	n/a	n/a
30	MAFK	chr4:3344272-3344470	HepG2	liver:	n/a	n/a
31	MAX	chr4:3344271-3344493	HepG2	liver:	n/a	n/a
32	MXI1	chr4:3344206-3344481	HepG2	liver:	n/a	n/a
33	MYC	chr4:3344360-3344380	HepG2	liver:	n/a	n/a
34	NR3C1	chr4:3345059-3345531	A549	lung:	n/a	n/a
35	NR3C1	chr4:3345037-3345543	A549	lung:	n/a	n/a
36	NR3C1	chr4:3344193-3344493	A549	lung:	n/a	n/a
37	NR3C1	chr4:3345202-3345441	A549	lung:	n/a	n/a
38	NR3C1	chr4:3344141-3344479	A549	lung:	n/a	n/a
39	NR3C1	chr4:3345077-3345540	A549	lung:	n/a	n/a
40	POLR2A	chr4:3343836-3344634	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr4:3343647-3343777	A549	lung:	n/a	n/a
42	POLR2A	chr4:3343907-3344427	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr4:3343839-3344282	SK-N-MC	brain:	n/a	n/a
44	POLR2A	chr4:3343817-3344447	HUVEC	blood vessel:	n/a	n/a
45	SP1	chr4:3344088-3344646	A549	lung:	n/a	n/a
46	SP1	chr4:3344084-3344650	A549	lung:	n/a	n/a
47	SP1	chr4:3344124-3344571	HepG2	liver:	n/a	n/a
48	TCF12	chr4:3343822-3344704	A549	lung:	n/a	n/a
49	USF1	chr4:3344220-3344444	HepG2	liver:	n/a	chr4:3344332-3344343

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3345374-3345424	HL-60	blood:	n/a
2	chr4:3345374-3345424	HL-60	blood:	n/a
3	chr4:3345374-3345424	MCF-7	breast:	n/a
4	chr4:3344154-3344204	HIPEpiC	eye:	n/a
5	chr4:3345495-3345545	T-47D	breast:	n/a
6	chr4:3345374-3345424	Hela-S3	cervix:	n/a
7	chr4:3345495-3345545	CMK	blood:	n/a
8	chr4:3344154-3344204	NB4	blood:	n/a
9	chr4:3344154-3344204	PrEC	prostate:	n/a
10	chr4:3345374-3345424	SAEC	small airway:	n/a
11	chr4:3345374-3345424	BJ	skin:	n/a
12	chr4:3345495-3345545	SK-N-SH	brain:	n/a
13	chr4:3345495-3345545	PANC-1	pancreas:	n/a
14	chr4:3345374-3345424	SK-N-SH_RA	brain:	n/a
15	chr4:3345495-3345545	RPTEC	kidney:	n/a
16	chr4:3345374-3345424	HNPCEpiC	eye:	n/a
17	chr4:3345495-3345545	Hela-S3	cervix:	n/a
18	chr4:3344154-3344204	PFSK-1	brain:	n/a
19	chr4:3344154-3344204	Hepatocyte	liver:	n/a
20	chr4:3345495-3345545	AoSMC	blood vessel:	n/a
21	chr4:3345374-3345424	NH-A	brain:	n/a
22	chr4:3345374-3345424	Caco-2	colon:	n/a
23	chr4:3344154-3344204	NHBE	bronchial:	n/a
24	chr4:3345374-3345424	IMR90	lung:	fetal
25	chr4:3344154-3344204	NT2-D1	testis:	n/a
26	chr4:3345374-3345424	SK-N-MC	brain:	n/a
27	chr4:3345495-3345545	HEEpiC	esophagus:	n/a
28	chr4:3345495-3345545	AG09319	gingival:	n/a
29	chr4:3345495-3345545	NT2-D1	testis:	n/a
30	chr4:3345495-3345545	HCF	heart:	n/a
31	chr4:3345374-3345424	U87	brain:	n/a
32	chr4:3344154-3344204	NHDF-neo	bronchial:	n/a
33	chr4:3344154-3344204	ECC-1	luminal epithelium:	n/a
34	chr4:3345495-3345545	HRCEpiC	kidney:	n/a
35	chr4:3345374-3345424	RPTEC	kidney:	n/a
36	chr4:3345495-3345545	A549	lung:	n/a
37	chr4:3345374-3345424	GM12891	blood:	n/a
38	chr4:3345374-3345424	SKMC	muscle:	n/a
39	chr4:3345374-3345424	AG04449	skin:	fetal
40	chr4:3345495-3345545	Caco-2	colon:	n/a
41	chr4:3345495-3345545	HCPEpiC	choroid plexus:	n/a
42	chr4:3345495-3345545	MCF10A-Er-Src	breast:	n/a
43	chr4:3345374-3345424	AG09319	gingival:	n/a
44	chr4:3345495-3345545	HRPEpiC	eye:	n/a
45	chr4:3345495-3345545	Jurkat	blood:	n/a
46	chr4:3345495-3345545	HL-60	blood:	n/a
47	chr4:3345374-3345424	HEK293	kidney:	embryo
48	chr4:3345495-3345545	HEK293	kidney:	embryo
49	chr4:3344154-3344204	HNPCEpiC	eye:	n/a
50	chr4:3344154-3344204	Jurkat	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3346041..3348825-chr4:3461682..3464499,2	MCF-7	breast:
2	chr4:3345074..3347959-chr4:3442893..3444446,2	MCF-7	breast:
3	chr4:3340754..3343218-chr4:3436055..3438880,2	MCF-7	breast:
4	chr4:3344329..3346374-chr4:3348112..3350683,2	K562	blood:
5	chr4:3339354..3341969-chr4:3342389..3344050,2	MCF-7	breast:
6	chr4:3338889..3343165-chr4:3463099..3467145,4	MCF-7	breast:
7	chr4:3344785..3347772-chr4:3481036..3482952,2	MCF-7	breast:
8	chr4:3292758..3295748-chr4:3341243..3344299,3	MCF-7	breast:
9	chr4:3343221..3349626-chr4:3462156..3471133,16	MCF-7	breast:
10	chr4:3345570..3349550-chr4:3443309..3446675,3	MCF-7	breast:
11	chr4:3341846..3343634-chr4:3447069..3448712,2	MCF-7	breast:

No data

Variant related genes	Relation type
RGS12	TF binding region
RGS12	CpG island
ENSG00000159788	chromatin interactions
ENSG00000109758	chromatin interactions
ENSG00000175920	chromatin interactions

Extended variants
information (count: 175 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:175 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568135717	chr4:3342961-3342962	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs150333585	chr4:3342964-3342965	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs185707879	chr4:3342997-3342998	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs71608275	chr4:3343033-3343034	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs190616736	chr4:3343164-3343165	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs111216105	chr4:3343173-3343174	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs6853606	chr4:3343206-3343207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs565785848	chr4:3343231-3343232	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs184271901	chr4:3343255-3343256	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs568324986	chr4:3343257-3343258	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs6839871	chr4:3343264-3343265	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs188804216	chr4:3343286-3343287	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs181265290	chr4:3343298-3343299	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs561616014	chr4:3343299-3343300	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs185276422	chr4:3343300-3343301	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs190812052	chr4:3343321-3343322	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs61324808	chr4:3343391-3343392	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs180889988	chr4:3343395-3343396	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs59211719	chr4:3343415-3343416	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs570535633	chr4:3343427-3343428	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs71608276	chr4:3343444-3343445	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs13130998	chr4:3343567-3343568	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs369573112	chr4:3343590-3343591	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs71608277	chr4:3343619-3343620	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138012733	chr4:3343660-3343661	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs572339506	chr4:3343673-3343674	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs571734958	chr4:3343675-3343676	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs539397975	chr4:3343688-3343689	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs559478016	chr4:3343691-3343692	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs115767912	chr4:3343709-3343710	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs187326422	chr4:3343712-3343713	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs114013828	chr4:3343724-3343725	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs555416283	chr4:3343726-3343727	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs149510811	chr4:3343727-3343728	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs111457016	chr4:3343734-3343735	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs564713745	chr4:3343754-3343755	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs372072142	chr4:3343760-3343761	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs192226500	chr4:3343797-3343798	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs567189743	chr4:3343844-3343845	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544137226	chr4:3343849-3343850	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs563638273	chr4:3343853-3343854	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs529308263	chr4:3343856-3343857	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs77765267	chr4:3343869-3343870	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs183266560	chr4:3343887-3343888	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs559783588	chr4:3343890-3343891	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs528619694	chr4:3343953-3343954	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs547566697	chr4:3343971-3343972	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs377636520	chr4:3343972-3343973	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs187601492	chr4:3344009-3344010	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs566072273	chr4:3344015-3344016	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3301200-3350000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:3314400-3348200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr4:3320000-3344000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr4:3320400-3351800	Weak transcription	Aorta	Aorta
5	chr4:3321000-3347000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr4:3323600-3344000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:3323600-3344800	Weak transcription	Fetal Intestine Large	intestine
8	chr4:3324000-3343600	Weak transcription	HSMM	muscle
9	chr4:3324200-3343600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:3325600-3348000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:3326400-3343600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr4:3326400-3343600	Weak transcription	NHLF	lung
13	chr4:3326400-3343800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr4:3326400-3344800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:3326400-3348000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:3328400-3343600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:3330200-3343600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr4:3331000-3343600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr4:3332400-3343800	Weak transcription	Fetal Intestine Small	intestine
20	chr4:3332800-3343600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr4:3332800-3343600	Weak transcription	Primary T cells from cord blood	blood
22	chr4:3332800-3343600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr4:3334000-3345800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:3334000-3370600	Weak transcription	Right Atrium	heart
25	chr4:3334400-3343600	Weak transcription	Adipose Nuclei	Adipose
26	chr4:3334600-3343600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr4:3337000-3344000	Weak transcription	Fetal Kidney	kidney
28	chr4:3337400-3343600	Weak transcription	Ovary	ovary
29	chr4:3337400-3343600	Weak transcription	Right Ventricle	heart
30	chr4:3337600-3343600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:3338200-3343600	Weak transcription	Brain Anterior Caudate	brain
32	chr4:3338400-3343600	Weak transcription	HepG2	liver
33	chr4:3338400-3343800	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr4:3339200-3353200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:3339800-3343600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:3339800-3343600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:3340200-3343200	Enhancers	Lung	lung
38	chr4:3340200-3344000	Enhancers	Brain Germinal Matrix	brain
39	chr4:3340400-3343600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:3340600-3343600	Weak transcription	Placenta	Placenta
41	chr4:3340800-3343600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:3340800-3344000	Enhancers	Fetal Brain Male	brain
43	chr4:3341000-3343000	Enhancers	Fetal Brain Female	brain
44	chr4:3341000-3343600	Weak transcription	HUVEC	blood vessel
45	chr4:3341200-3343600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr4:3341200-3343600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:3341800-3343000	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr4:3342000-3344000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:3342000-3345200	Weak transcription	Gastric	stomach
50	chr4:3342000-3348200	Weak transcription	Brain Angular Gyrus	brain

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