Variant report

Variant	nsv966532
Chromosome Location	chr4:99571460-99581225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:457)
CpG islands
(count:671)
Chromatin interactive
region (count:4)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:99580038-99580493	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:99579570-99579588	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr4:99574896-99576044	HCT-116	colon:	n/a	chr4:99575721-99575732
4	CCNT2	chr4:99579391-99580028	K562	blood:	n/a	chr4:99579968-99579977
5	CEBPB	chr4:99574206-99574538	IMR90	lung:	n/a	n/a
6	CEBPB	chr4:99580962-99581836	HCT-116	colon:	n/a	n/a
7	CEBPB	chr4:99574855-99576128	HCT-116	colon:	n/a	n/a
8	CEBPB	chr4:99581010-99581872	HCT-116	colon:	n/a	n/a
9	CEBPB	chr4:99578730-99578996	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:99581219-99581664	A549	lung:	n/a	n/a
11	CEBPB	chr4:99578611-99579075	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:99581194-99581720	MCF-7	breast:	n/a	n/a
13	CHD1	chr4:99579448-99579576	GM12878	blood:	n/a	n/a
14	CHD1	chr4:99580280-99580444	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr4:99579139-99579727	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr4:99578523-99578588	GM12878	blood:	n/a	n/a
17	CHD2	chr4:99578890-99579722	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr4:99580022-99580730	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr4:99579621-99580151	A549	lung:	n/a	n/a
20	CTBP2	chr4:99578768-99580714	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr4:99579000-99579150	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr4:99580160-99580310	HVMF	connective:	n/a	chr4:99580228-99580241
23	CTCF	chr4:99574060-99574210	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr4:99580380-99580530	HCT-116	colon:	n/a	n/a
25	CTCF	chr4:99578820-99578970	GM12874	blood:	n/a	n/a
26	CTCF	chr4:99580580-99580730	BJ	skin:	n/a	n/a
27	CTCF	chr4:99580340-99580490	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr4:99579360-99579510	GM12871	blood:	n/a	n/a
29	CTCF	chr4:99580140-99580290	HEK293	kidney:	n/a	chr4:99580228-99580241
30	CTCF	chr4:99574000-99574150	BJ	skin:	n/a	n/a
31	CTCF	chr4:99578920-99579070	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr4:99579870-99579892	GM10266	blood:	n/a	n/a
33	CTCF	chr4:99580300-99580450	HVMF	connective:	n/a	n/a
34	CTCF	chr4:99580400-99580550	RPTEC	kidney:	n/a	n/a
35	CTCF	chr4:99580360-99580510	NHLF	lung:	n/a	n/a
36	CTCF	chr4:99580360-99580510	SAEC	small airway:	n/a	n/a
37	CTCF	chr4:99580280-99580490	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr4:99580394-99580476	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr4:99580280-99580430	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr4:99580360-99580510	HAc	cerebellar:	n/a	n/a
41	CTCF	chr4:99579919-99579943	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:99579934-99579970	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:99580380-99580530	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr4:99579876-99580487	GM12878	blood:	n/a	chr4:99580228-99580241
45	CTCF	chr4:99580000-99580150	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr4:99580400-99580500	NHEK	skin:	n/a	n/a
47	CTCF	chr4:99579900-99580050	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr4:99580280-99580430	HCM	heart:	n/a	n/a
49	CTCF	chr4:99580260-99580410	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr4:99580340-99580490	BJ	skin:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99580530-99580580	NHBE	bronchial:	n/a
2	chr4:99580121-99580171	HMEC	breast:	n/a
3	chr4:99579971-99580021	SKMC	muscle:	n/a
4	chr4:99578720-99578770	A549	lung:	n/a
5	chr4:99579248-99579298	HAEpiC	amniotic membrane:	n/a
6	chr4:99580530-99580580	MCF-7	breast:	n/a
7	chr4:99579615-99579665	HEK293	kidney:	embryo
8	chr4:99579615-99579665	HIPEpiC	eye:	n/a
9	chr4:99577266-99577316	NHBE	bronchial:	n/a
10	chr4:99579615-99579665	HUVEC	blood vessel:	n/a
11	chr4:99577266-99577316	GM12878	blood:	n/a
12	chr4:99577266-99577316	CMK	blood:	n/a
13	chr4:99578720-99578770	HNPCEpiC	eye:	n/a
14	chr4:99579971-99580021	HNPCEpiC	eye:	n/a
15	chr4:99580449-99580499	BJ	skin:	n/a
16	chr4:99579248-99579298	HMEC	breast:	n/a
17	chr4:99577266-99577316	MCF-7	breast:	n/a
18	chr4:99579971-99580021	PANC-1	pancreas:	n/a
19	chr4:99579971-99580021	LNCaP	prostate:	n/a
20	chr4:99577266-99577316	NHDF-neo	bronchial:	n/a
21	chr4:99580530-99580580	SK-N-SH_RA	brain:	n/a
22	chr4:99579248-99579298	U87	brain:	n/a
23	chr4:99580530-99580580	SKMC	muscle:	n/a
24	chr4:99578720-99578770	NT2-D1	testis:	n/a
25	chr4:99580121-99580171	AG09309	skin:	n/a
26	chr4:99580143-99580193	ProgFib	skin:	n/a
27	chr4:99579971-99580021	GM06990	blood:	n/a
28	chr4:99577266-99577316	HCF	heart:	n/a
29	chr4:99580449-99580499	BE2_C	brain:	n/a
30	chr4:99576808-99576858	HRCEpiC	kidney:	n/a
31	chr4:99578720-99578770	LNCaP	prostate:	n/a
32	chr4:99580530-99580580	SK-N-MC	brain:	n/a
33	chr4:99580143-99580193	RPTEC	kidney:	n/a
34	chr4:99577266-99577316	HAEpiC	amniotic membrane:	n/a
35	chr4:99580849-99580899	H1-hESC	embryonic stem cell:	embryo
36	chr4:99580849-99580899	AoSMC	blood vessel:	n/a
37	chr4:99576808-99576858	BJ	skin:	n/a
38	chr4:99580530-99580580	HCT-116	colon:	n/a
39	chr4:99579971-99580021	HEK293	kidney:	embryo
40	chr4:99580849-99580899	HUVEC	blood vessel:	n/a
41	chr4:99580121-99580171	K562	blood:	n/a
42	chr4:99579615-99579665	HCT-116	colon:	n/a
43	chr4:99580121-99580171	MCF-7	breast:	n/a
44	chr4:99579248-99579298	RPTEC	kidney:	n/a
45	chr4:99580121-99580171	HCF	heart:	n/a
46	chr4:99580849-99580899	NT2-D1	testis:	n/a
47	chr4:99580121-99580171	Jurkat	blood:	n/a
48	chr4:99580849-99580899	Jurkat	blood:	n/a
49	chr4:99579971-99580021	Caco-2	colon:	n/a
50	chr4:99580849-99580899	HRCEpiC	kidney:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:99566031..99568525-chr4:99568795..99571513,2	MCF-7	breast:
2	chr4:99180743..99183219-chr4:99577927..99581407,3	MCF-7	breast:
3	chr4:99575715..99578300-chr4:99579443..99581307,2	K562	blood:
4	chr4:99181647..99184072-chr4:99579310..99582613,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAP1GDS1-3	chr4:99580055-99585702	NONHSAT097492
2	lnc-RAP1GDS1-3	chr4:99580055-99585701	ENSG00000260641.1
3	lnc-RAP1GDS1-3	chr4:99580077-99580173	XLOC_003615
4	lnc-RAP1GDS1-3	chr4:99579918-99580023	XLOC_003615
5	lnc-RAP1GDS1-3	chr4:99580983-99582077	XLOC_003615

No data

Variant related genes	Relation type
ENSG00000260641	TF binding region
TSPAN5	TF binding region
ENSG00000260641	CpG island
TSPAN5	CpG island
ENSG00000138698	chromatin interactions
ENSG00000214559	chromatin interactions
ENSG00000168785	chromatin interactions
ENSG00000260641	chromatin interactions
NRAS	miRNA target sites

Extended variants
information (count: 293 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74766783	chr4:99571518-99571519	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191378653	chr4:99571566-99571567	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183907811	chr4:99571609-99571610	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551144030	chr4:99571651-99571652	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs59870493	chr4:99571678-99571679	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569352768	chr4:99571679-99571680	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs57055920	chr4:99571680-99571681	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549164711	chr4:99571705-99571706	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76201340	chr4:99571706-99571707	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534566899	chr4:99571720-99571721	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116417252	chr4:99571739-99571740	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577606189	chr4:99571757-99571758	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77473051	chr4:99571771-99571772	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527949113	chr4:99571807-99571808	Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556664069	chr4:99571915-99571916	Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72900208	chr4:99571938-99571939	Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs542825619	chr4:99572016-99572017	Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561114827	chr4:99572032-99572033	Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138075810	chr4:99572088-99572089	Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540612650	chr4:99572207-99572208	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534764284	chr4:99572234-99572235	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529524988	chr4:99572243-99572244	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532430828	chr4:99572322-99572323	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188687746	chr4:99572379-99572380	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562987943	chr4:99572413-99572414	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181536446	chr4:99572435-99572436	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549203204	chr4:99572448-99572449	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549431069	chr4:99572462-99572463	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567308843	chr4:99572466-99572467	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534806760	chr4:99572485-99572486	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546624256	chr4:99572499-99572500	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571494924	chr4:99572588-99572589	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567491656	chr4:99572651-99572652	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376756457	chr4:99572653-99572654	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187162737	chr4:99572682-99572683	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556503267	chr4:99572701-99572702	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4699663	chr4:99572723-99572724	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs535895197	chr4:99572753-99572754	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554642389	chr4:99572785-99572786	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549847946	chr4:99572793-99572794	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540802329	chr4:99572831-99572832	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs571448828	chr4:99572836-99572837	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs559023481	chr4:99572875-99572876	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs538652545	chr4:99572923-99572924	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs554088401	chr4:99572959-99572960	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs373098799	chr4:99573014-99573015	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs76356370	chr4:99573015-99573016	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs552597633	chr4:99573038-99573039	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs577434079	chr4:99573077-99573078	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs544640380	chr4:99573148-99573149	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	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
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
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:877 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99548000-99577000	Weak transcription	Esophagus	oesophagus
2	chr4:99564000-99571600	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr4:99564400-99575600	Weak transcription	Fetal Kidney	kidney
4	chr4:99566000-99575200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr4:99567600-99574200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr4:99567600-99574400	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr4:99567600-99574800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr4:99568200-99571600	Enhancers	Fetal Brain Female	brain
9	chr4:99568200-99571600	Enhancers	NHDF-Ad	bronchial
10	chr4:99568400-99575000	Weak transcription	Thymus	Thymus
11	chr4:99569600-99578200	Weak transcription	Aorta	Aorta
12	chr4:99569600-99578400	Weak transcription	Spleen	Spleen
13	chr4:99569800-99571600	Enhancers	Brain Cingulate Gyrus	brain
14	chr4:99570000-99576800	Weak transcription	Fetal Stomach	stomach
15	chr4:99570200-99571600	Enhancers	Osteobl	bone
16	chr4:99570200-99571800	Weak transcription	HMEC	breast
17	chr4:99570200-99573800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:99570200-99573800	Weak transcription	Fetal Brain Male	brain
19	chr4:99570200-99577000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:99570200-99577000	Weak transcription	Fetal Heart	heart
21	chr4:99570400-99573800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:99570600-99572000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr4:99570600-99572200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr4:99570600-99573800	Weak transcription	Brain Hippocampus Middle	brain
25	chr4:99570800-99571600	ZNF genes & repeats	NHLF	lung
26	chr4:99571000-99571800	Enhancers	Brain Angular Gyrus	brain
27	chr4:99571000-99573600	Weak transcription	NH-A	brain
28	chr4:99571000-99574200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr4:99571200-99571600	Weak transcription	HSMM	muscle
30	chr4:99571200-99572000	ZNF genes & repeats	HUVEC	blood vessel
31	chr4:99571200-99572200	ZNF genes & repeats	A549	lung
32	chr4:99571200-99572800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:99571200-99573600	Weak transcription	Brain Anterior Caudate	brain
34	chr4:99571200-99574000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr4:99571200-99574000	Weak transcription	Brain Substantia Nigra	brain
36	chr4:99571200-99574400	Weak transcription	Ovary	ovary
37	chr4:99571400-99571600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr4:99571400-99571600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:99571400-99571800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:99571400-99572400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:99571400-99572600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
42	chr4:99571400-99572600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr4:99571400-99573000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr4:99571400-99573400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
45	chr4:99571600-99572000	ZNF genes & repeats	HSMM	muscle
46	chr4:99571600-99572400	Weak transcription	Brain Cingulate Gyrus	brain
47	chr4:99571600-99573400	Weak transcription	NHLF	lung
48	chr4:99571600-99573600	Weak transcription	Osteobl	bone
49	chr4:99571600-99574000	Weak transcription	Fetal Brain Female	brain
50	chr4:99571600-99574600	Weak transcription	Brain Inferior Temporal Lobe	brain

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