Variant report

Variant	nsv879849
Chromosome Location	chr4:120823634-120922444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:120901457-120901478	GM12878	blood:	n/a	n/a
2	CEBPB	chr4:120922073-120922396	IMR90	lung:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
3	CEBPB	chr4:120922133-120922389	A549	lung:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
4	CEBPB	chr4:120922026-120922449	MCF-7	breast:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
5	CEBPB	chr4:120836780-120837042	HepG2	liver:	n/a	chr4:120836903-120836914
6	CEBPB	chr4:120867550-120867816	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:120860325-120860620	IMR90	lung:	n/a	chr4:120860465-120860478 chr4:120860467-120860478
8	CEBPB	chr4:120922073-120922387	HepG2	liver:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
9	CEBPB	chr4:120922082-120922311	H1-hESC	embryonic stem cell:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
10	CEBPB	chr4:120825084-120825135	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:120889537-120889720	A549	lung:	n/a	chr4:120889600-120889611 chr4:120889598-120889611 chr4:120889598-120889611
12	CEBPB	chr4:120836776-120837011	IMR90	lung:	n/a	chr4:120836903-120836914
13	CEBPB	chr4:120922126-120922326	K562	blood:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
14	CEBPB	chr4:120862712-120862988	IMR90	lung:	n/a	chr4:120862878-120862895
15	CEBPB	chr4:120922065-120922388	Hela-S3	cervix:	n/a	chr4:120922212-120922221 chr4:120922212-120922223 chr4:120922210-120922221
16	CHD1	chr4:120915931-120916139	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr4:120921737-120921912	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr4:120855791-120855855	Fibrobl	skin:	n/a	n/a
19	CTCF	chr4:120828879-120828993	GM13977	blood:	n/a	n/a
20	CTCF	chr4:120827916-120827936	LNCaP	prostate:	n/a	n/a
21	CTCF	chr4:120877474-120877514	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr4:120904560-120904710	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr4:120835500-120835650	GM12865	blood:	n/a	n/a
24	CTCF	chr4:120881339-120881436	Lung_OC	lung:	n/a	n/a
25	CTCF	chr4:120828103-120828141	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr4:120876560-120876710	HCPEpiC	choroid plexus:	n/a	n/a
27	EBF1	chr4:120832284-120832484	GM12878	blood:	n/a	n/a
28	EGR1	chr4:120875659-120875863	GM12878	blood:	n/a	n/a
29	EP300	chr4:120825643-120825722	K562	blood:	n/a	n/a
30	FOS	chr4:120867580-120867703	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr4:120902307-120902434	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr4:120867617-120867765	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr4:120851675-120851830	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr4:120867580-120867780	MCF10A-Er-Src	breast:	n/a	n/a
35	FOXA2	chr4:120875076-120875770	A549	lung:	n/a	n/a
36	FOXA2	chr4:120875319-120875668	A549	lung:	n/a	n/a
37	FOXA2	chr4:120919602-120920068	A549	lung:	n/a	n/a
38	GATA2	chr4:120922185-120922446	SH-SY5Y	brain:	n/a	chr4:120922271-120922280
39	GATA3	chr4:120921928-120922673	MCF-7	breast:	n/a	chr4:120922271-120922280
40	GATA3	chr4:120922042-120922389	MCF-7	breast:	n/a	chr4:120922271-120922280
41	GATA3	chr4:120921992-120922489	MCF-7	breast:	n/a	chr4:120922271-120922280
42	HEY1	chr4:120875661-120875906	K562	blood:	n/a	n/a
43	JUN	chr4:120860500-120860644	HepG2	liver:	n/a	chr4:120860586-120860595
44	JUN	chr4:120880214-120880441	HepG2	liver:	n/a	chr4:120880335-120880348 chr4:120880336-120880345
45	JUN	chr4:120848270-120848274	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUN	chr4:120908348-120908441	K562	blood:	n/a	n/a
47	JUND	chr4:120907981-120908010	HepG2	liver:	n/a	n/a
48	JUND	chr4:120880192-120880481	HepG2	liver:	n/a	chr4:120880336-120880345
49	KAP1	chr4:120921732-120922607	HEK293	kidney:	n/a	n/a
50	KAP1	chr4:120921933-120922702	U2OS	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120860309-120860359	Hepatocyte	liver:	n/a
2	chr4:120860309-120860359	A549	lung:	n/a
3	chr4:120915594-120915644	BE2_C	brain:	n/a
4	chr4:120915594-120915644	HMEC	breast:	n/a
5	chr4:120860309-120860359	PFSK-1	brain:	n/a
6	chr4:120860309-120860359	LNCaP	prostate:	n/a
7	chr4:120915594-120915644	GM19239	blood:	n/a
8	chr4:120898808-120898858	CMK	blood:	n/a
9	chr4:120860309-120860359	MCF-7	breast:	n/a
10	chr4:120915594-120915644	BJ	skin:	n/a
11	chr4:120860309-120860359	NH-A	brain:	n/a
12	chr4:120898808-120898858	Hela-S3	cervix:	n/a
13	chr4:120898808-120898858	AG09319	gingival:	n/a
14	chr4:120915594-120915644	HepG2	liver:	n/a
15	chr4:120860309-120860359	HepG2	liver:	n/a
16	chr4:120915594-120915644	ovcar-3	ovarian:	n/a
17	chr4:120898808-120898858	GM19239	blood:	n/a
18	chr4:120898808-120898858	H1-hESC	embryonic stem cell:	embryo
19	chr4:120898808-120898858	NHBE	bronchial:	n/a
20	chr4:120898808-120898858	HUVEC	blood vessel:	n/a
21	chr4:120860309-120860359	IMR90	lung:	fetal
22	chr4:120898808-120898858	Caco-2	colon:	n/a
23	chr4:120898808-120898858	ECC-1	luminal epithelium:	n/a
24	chr4:120898808-120898858	GM12891	blood:	n/a
25	chr4:120915594-120915644	A549	lung:	n/a
26	chr4:120898808-120898858	MCF10A-Er-Src	breast:	n/a
27	chr4:120860309-120860359	GM19239	blood:	n/a
28	chr4:120898808-120898858	Jurkat	blood:	n/a
29	chr4:120860309-120860359	ECC-1	luminal epithelium:	n/a
30	chr4:120860309-120860359	NT2-D1	testis:	n/a
31	chr4:120860309-120860359	AG04449	skin:	fetal
32	chr4:120915594-120915644	HUVEC	blood vessel:	n/a
33	chr4:120898808-120898858	HRCEpiC	kidney:	n/a
34	chr4:120898808-120898858	NT2-D1	testis:	n/a
35	chr4:120915594-120915644	Hela-S3	cervix:	n/a
36	chr4:120915594-120915644	NHDF-neo	bronchial:	n/a
37	chr4:120860309-120860359	GM12891	blood:	n/a
38	chr4:120915594-120915644	AG04449	skin:	fetal
39	chr4:120860309-120860359	AoSMC	blood vessel:	n/a
40	chr4:120915594-120915644	RPTEC	kidney:	n/a
41	chr4:120898808-120898858	LNCaP	prostate:	n/a
42	chr4:120860309-120860359	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:120915594-120915644	MCF-7	breast:	n/a
44	chr4:120898808-120898858	NHDF-neo	bronchial:	n/a
45	chr4:120860309-120860359	AG09319	gingival:	n/a
46	chr4:120898808-120898858	HepG2	liver:	n/a
47	chr4:120860309-120860359	GM12878	blood:	n/a
48	chr4:120898808-120898858	HCF	heart:	n/a
49	chr4:120898808-120898858	HEK293	kidney:	embryo
50	chr4:120915594-120915644	H1-hESC	embryonic stem cell:	embryo

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120898790..120900807-chr4:120905834..120908765,2	K562	blood:
2	chr4:120860025..120863004-chr4:120864528..120867684,3	K562	blood:
3	chr4:120883690..120886191-chr4:120886858..120889545,2	K562	blood:
4	chr4:120892542..120895411-chr4:120896318..120898714,2	MCF-7	breast:
5	chr4:120899347..120901114-chr4:120901609..120903898,2	MCF-7	breast:
6	chr4:120818918..120821207-chr4:120823634..120826581,2	K562	blood:
7	chr4:120898790..120900807-chr4:120905834..120908765,2	K562	blood:
8	chr4:120853485..120855986-chr4:120857672..120860298,2	K562	blood:
9	chr4:120883690..120886191-chr4:120886858..120889545,2	K562	blood:
10	chr4:120892542..120895411-chr4:120896318..120898714,2	MCF-7	breast:
11	chr4:120899347..120901114-chr4:120901609..120903898,2	MCF-7	breast:
12	chr4:120921343..120923138-chr4:120927262..120929036,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-5	chr4:120860695-120860830	ENSG00000250392.2
2	lnc-AC110373.1-5	chr4:120884943-120885385	NONHSAT098107
3	lnc-AC110373.1-5	chr4:120860785-120860830	NONHSAT098110
4	lnc-AC110373.1-5	chr4:120885151-120885352	NONHSAT098110
5	lnc-AC110373.1-5	chr4:120853610-120853772	NONHSAT098107
6	lnc-AC110373.1-5	chr4:120884943-120885448	ENSG00000250392.2
7	lnc-AC110373.1-5	chr4:120884943-120885053	NONHSAT098110
8	lnc-AC110373.1-5	chr4:120884943-120885376	ENSG00000250392.1
9	lnc-AC110373.1-5	chr4:120860695-120860830	ENSG00000250392.1

No data

Variant related genes	Relation type
ENSG00000250392	TF binding region
ENSG00000200553	TF binding region
ENSG00000250183	TF binding region
ENSG00000250392	CpG island
ENSG00000200553	CpG island
ENSG00000250183	CpG island
ENSG00000250183	chromatin interactions
ENSG00000250392	chromatin interactions

Extended variants
information (count: 2390 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2390 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377164204	chr4:120850849-120850850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146044831	chr4:120850887-120850888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556251505	chr4:120850932-120850933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372274455	chr4:120850934-120850935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566309202	chr4:120850963-120850964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2160499	chr4:120850972-120850973	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549022401	chr4:120850979-120850980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77518745	chr4:120851048-120851049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77109037	chr4:120851091-120851092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558779049	chr4:120851109-120851110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572429030	chr4:120851130-120851131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4834826	chr4:120851140-120851141	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs138729838	chr4:120851171-120851172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546057938	chr4:120851204-120851205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141156809	chr4:120851220-120851221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574278473	chr4:120851225-120851226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542865287	chr4:120851226-120851227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193233199	chr4:120851260-120851261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150710630	chr4:120851327-120851328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111659695	chr4:120851344-120851345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564922399	chr4:120851365-120851366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527708203	chr4:120851395-120851396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139104689	chr4:120851403-120851404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149912309	chr4:120851424-120851425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs72914303	chr4:120851438-120851439	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs548926701	chr4:120851481-120851482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs924752	chr4:120853499-120853500	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182319179	chr4:120853587-120853588	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs58506198	chr4:120853622-120853623	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs10518345	chr4:120853647-120853648	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs72684560	chr4:120853650-120853651	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs115177035	chr4:120853662-120853663	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs534925550	chr4:120853695-120853696	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs548349182	chr4:120853696-120853697	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs375313812	chr4:120853709-120853710	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs568541604	chr4:120853777-120853778	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185470670	chr4:120853836-120853837	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372813608	chr4:120853867-120853868	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs75627812	chr4:120853901-120853902	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12500708	chr4:120853983-120853984	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs144736802	chr4:120854020-120854021	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs72684561	chr4:120854042-120854043	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538915394	chr4:120854064-120854065	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558940060	chr4:120854171-120854172	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189834526	chr4:120854238-120854239	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541230704	chr4:120854288-120854289	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560775930	chr4:120854296-120854297	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574489829	chr4:120854299-120854300	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543186241	chr4:120854301-120854302	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563272995	chr4:120854310-120854311	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Esophageal squamous carcinoma	18350619	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	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
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Myelodysplastic syndrome	18508791	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120850800-120851600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:120854200-120855000	Enhancers	Fetal Kidney	kidney
3	chr4:120855200-120855600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr4:120859200-120859800	Enhancers	Aorta	Aorta
5	chr4:120859200-120860400	Enhancers	Fetal Heart	heart
6	chr4:120859400-120861400	Enhancers	Osteobl	bone
7	chr4:120859600-120860000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:120859600-120861000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:120859600-120861000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:120859800-120860800	Weak transcription	Aorta	Aorta
11	chr4:120859800-120861000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr4:120860000-120860200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr4:120860000-120860200	Enhancers	Brain Anterior Caudate	brain
14	chr4:120860200-120861200	Enhancers	Brain Substantia Nigra	brain
15	chr4:120860400-120860600	Flanking Active TSS	Fetal Heart	heart
16	chr4:120860600-120861200	Active TSS	Skeletal Muscle Male	skeletal muscle
17	chr4:120860600-120861800	Active TSS	Fetal Heart	heart
18	chr4:120860600-120862000	Active TSS	Right Ventricle	heart
19	chr4:120860600-120863000	Active TSS	Right Atrium	heart
20	chr4:120860800-120861000	Enhancers	Aorta	Aorta
21	chr4:120860800-120861200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:120860800-120861200	Active TSS	Left Ventricle	heart
23	chr4:120861000-120862600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:120861200-120861600	Weak transcription	Brain Substantia Nigra	brain
25	chr4:120861200-120861800	Weak transcription	Left Ventricle	heart
26	chr4:120861600-120861800	Enhancers	Brain Anterior Caudate	brain
27	chr4:120861600-120862000	Enhancers	Brain Substantia Nigra	brain
28	chr4:120861800-120862000	Active TSS	Left Ventricle	heart
29	chr4:120861800-120862400	Weak transcription	Fetal Heart	heart
30	chr4:120862400-120862800	Enhancers	Fetal Heart	heart
31	chr4:120862600-120863200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr4:120862800-120864000	Weak transcription	Fetal Heart	heart
33	chr4:120863000-120863200	Enhancers	Right Atrium	heart
34	chr4:120864000-120865200	Enhancers	Fetal Heart	heart
35	chr4:120865400-120865800	Enhancers	HepG2	liver
36	chr4:120867600-120867800	Enhancers	Left Ventricle	heart
37	chr4:120868200-120868600	Enhancers	Left Ventricle	heart
38	chr4:120875600-120876000	Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr4:120875600-120876200	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr4:120875800-120876800	Enhancers	H1 Cell Line	embryonic stem cell
41	chr4:120876000-120876200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr4:120876000-120876600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr4:120876200-120876400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr4:120876200-120876400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:120876200-120876800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr4:120876200-120877200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr4:120876600-120881600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr4:120881600-120883200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr4:120882200-120882600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr4:120882200-120883200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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