Variant report

Variant	nsv829877
Chromosome Location	chr4:20847465-20992544
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:219)
CpG islands
(count:978)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:219 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:20865610-20865795	K562	blood:	n/a	n/a
2	BACH1	chr4:20985747-20986024	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr4:20926759-20926809	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr4:20941568-20941822	A549	lung:	n/a	chr4:20941702-20941715 chr4:20941704-20941713 chr4:20941704-20941713 chr4:20941704-20941713
5	CEBPB	chr4:20964373-20964561	HepG2	liver:	n/a	chr4:20964441-20964452 chr4:20964440-20964453 chr4:20964440-20964451
6	CEBPB	chr4:20941551-20941842	HepG2	liver:	n/a	chr4:20941702-20941715 chr4:20941704-20941713 chr4:20941704-20941713 chr4:20941704-20941713
7	CEBPB	chr4:20937960-20938160	HepG2	liver:	n/a	chr4:20938070-20938081
8	CTCF	chr4:20888220-20888370	Caco-2	colon:	n/a	n/a
9	CTCF	chr4:20861167-20861202	GM20000	blood:	n/a	n/a
10	CTCF	chr4:20887060-20887210	AG10803	skin:	n/a	n/a
11	CTCF	chr4:20849882-20849918	Spleen_OC	spleen:	n/a	n/a
12	CTCF	chr4:20988940-20989090	HMEC	breast:	n/a	chr4:20989007-20989028
13	CTCF	chr4:20853039-20853074	LNCaP	prostate:	n/a	n/a
14	CTCF	chr4:20895249-20895335	GM10266	blood:	n/a	n/a
15	CTCF	chr4:20912316-20912408	Lung_OC	lung:	n/a	n/a
16	CTCF	chr4:20961980-20962130	HRE	kidney:	n/a	n/a
17	CTCF	chr4:20856260-20856410	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr4:20988900-20989050	MCF-7	breast:	n/a	chr4:20989007-20989028
19	CTCF	chr4:20847320-20847470	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr4:20988780-20988930	Caco-2	colon:	n/a	n/a
21	CTCF	chr4:20948851-20948961	GM20000	blood:	n/a	n/a
22	CTCF	chr4:20988957-20989064	HUVEC	blood vessel:	n/a	chr4:20989007-20989028
23	E2F4	chr4:20931065-20931386	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr4:20887479-20887858	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr4:20974328-20974392	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr4:20904678-20905009	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr4:20988717-20988883	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr4:20890891-20891000	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr4:20849214-20849414	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F6	chr4:20985706-20986100	H1-hESC	embryonic stem cell:	n/a	n/a
31	E2F6	chr4:20985597-20986140	H1-hESC	embryonic stem cell:	n/a	n/a
32	EP300	chr4:20860634-20861033	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr4:20956177-20956603	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr4:20955628-20956978	SK-N-SH	brain:	n/a	n/a
35	EP300	chr4:20956144-20956608	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr4:20860393-20861844	SK-N-SH	brain:	n/a	chr4:20861215-20861222 chr4:20861675-20861689
37	EP300	chr4:20860685-20861050	SK-N-SH_RA	brain:	n/a	n/a
38	FOS	chr4:20892448-20892668	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:20946750-20946752	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:20848730-20849051	MCF10A-Er-Src	breast:	n/a	chr4:20848869-20848880
41	FOS	chr4:20988946-20989146	MCF10A-Er-Src	breast:	n/a	chr4:20988972-20988980 chr4:20988970-20988982
42	FOS	chr4:20848803-20849036	MCF10A-Er-Src	breast:	n/a	chr4:20848869-20848880
43	FOS	chr4:20991326-20991329	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr4:20893238-20893372	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr4:20978746-20978967	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr4:20893172-20893452	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr4:20978834-20978969	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr4:20978835-20978906	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr4:20978787-20979007	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr4:20848756-20848927	MCF10A-Er-Src	breast:	n/a	chr4:20848869-20848880

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20884431-20884481	BJ	skin:	n/a
2	chr4:20985623-20985673	AoSMC	blood vessel:	n/a
3	chr4:20884431-20884481	BJ	skin:	n/a
4	chr4:20985623-20985673	AoSMC	blood vessel:	n/a
5	chr4:20852672-20852722	SKMC	muscle:	n/a
6	chr4:20986246-20986296	MCF-7	breast:	n/a
7	chr4:20884385-20884435	GM12892	blood:	n/a
8	chr4:20884385-20884435	HRE	kidney:	n/a
9	chr4:20986246-20986296	ECC-1	luminal epithelium:	n/a
10	chr4:20852337-20852387	HRCEpiC	kidney:	n/a
11	chr4:20885019-20885069	HCF	heart:	n/a
12	chr4:20884321-20884371	HCT-116	colon:	n/a
13	chr4:20960712-20960762	Hepatocyte	liver:	n/a
14	chr4:20985696-20985746	PANC-1	pancreas:	n/a
15	chr4:20884431-20884481	H1-hESC	embryonic stem cell:	embryo
16	chr4:20985984-20986034	PANC-1	pancreas:	n/a
17	chr4:20884431-20884481	A549	lung:	n/a
18	chr4:20985696-20985746	H1-hESC	embryonic stem cell:	embryo
19	chr4:20884321-20884371	ovcar-3	ovarian:	n/a
20	chr4:20852366-20852416	AG09309	skin:	n/a
21	chr4:20852366-20852416	A549	lung:	n/a
22	chr4:20985927-20985977	SK-N-SH	brain:	n/a
23	chr4:20988275-20988325	SAEC	small airway:	n/a
24	chr4:20985984-20986034	SK-N-SH	brain:	n/a
25	chr4:20988275-20988325	NB4	blood:	n/a
26	chr4:20884385-20884435	GM06990	blood:	n/a
27	chr4:20986246-20986296	SK-N-SH_RA	brain:	n/a
28	chr4:20852337-20852387	HCF	heart:	n/a
29	chr4:20884385-20884435	SK-N-MC	brain:	n/a
30	chr4:20885019-20885069	H1-hESC	embryonic stem cell:	embryo
31	chr4:20985984-20986034	NB4	blood:	n/a
32	chr4:20986246-20986296	HCT-116	colon:	n/a
33	chr4:20985927-20985977	HIPEpiC	eye:	n/a
34	chr4:20985696-20985746	HEEpiC	esophagus:	n/a
35	chr4:20885019-20885069	PANC-1	pancreas:	n/a
36	chr4:20985696-20985746	BE2_C	brain:	n/a
37	chr4:20960712-20960762	GM12878	blood:	n/a
38	chr4:20885246-20885296	CMK	blood:	n/a
39	chr4:20988275-20988325	SK-N-MC	brain:	n/a
40	chr4:20885246-20885296	A549	lung:	n/a
41	chr4:20985623-20985673	PFSK-1	brain:	n/a
42	chr4:20884385-20884435	NHDF-neo	bronchial:	n/a
43	chr4:20852366-20852416	MCF-7	breast:	n/a
44	chr4:20885536-20885586	CMK	blood:	n/a
45	chr4:20985623-20985673	HEK293	kidney:	embryo
46	chr4:20985984-20986034	AG10803	skin:	n/a
47	chr4:20960712-20960762	Jurkat	blood:	n/a
48	chr4:20884431-20884481	NHBE	bronchial:	n/a
49	chr4:20960712-20960762	HCF	heart:	n/a
50	chr4:20985696-20985746	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:20849276..20852275-chr6:109770823..109773619,2	K562	blood:
2	chr4:20966569..20968200-chr4:20971149..20973804,2	K562	blood:
3	chr1:147804723..147806420-chr4:20979153..20981320,2	MCF-7	breast:
4	chr4:20971332..20974110-chr4:20975805..20978136,2	K562	blood:
5	chr4:20940626..20942127-chr4:20945526..20948025,2	K562	blood:
6	chr4:20971332..20974110-chr4:20975805..20978136,2	K562	blood:
7	chr4:20779088..20780993-chr4:20896835..20899396,2	K562	blood:
8	chr4:20966569..20968200-chr4:20971149..20973804,2	K562	blood:
9	chr4:20940626..20942127-chr4:20945526..20948025,2	K562	blood:

No data

Variant related genes	Relation type
KCNIP4	TF binding region
KCNIP4	CpG island
ENSG00000135596	chromatin interactions

Extended variants
information (count: 3135 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3135 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55934998	chr4:20847504-20847505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144245300	chr4:20847521-20847522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534002434	chr4:20847560-20847561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189427446	chr4:20847594-20847595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374900347	chr4:20847616-20847617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116262608	chr4:20847619-20847620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10010160	chr4:20847620-20847621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs73802367	chr4:20847657-20847658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs10000529	chr4:20847663-20847664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs75870570	chr4:20847681-20847682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192520163	chr4:20847703-20847704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553253109	chr4:20847710-20847711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4697191	chr4:20847726-20847727	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs535777370	chr4:20847740-20847741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140058199	chr4:20847829-20847830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555043082	chr4:20847834-20847835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546420538	chr4:20847844-20847845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564510725	chr4:20847932-20847933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs79524989	chr4:20847955-20847956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79973172	chr4:20847992-20847993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561819660	chr4:20848035-20848036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543870080	chr4:20848063-20848064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11942985	chr4:20848085-20848086	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs75116946	chr4:20848103-20848104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143705216	chr4:20848114-20848115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184813472	chr4:20848173-20848174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189729897	chr4:20848188-20848189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377504730	chr4:20848189-20848190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56330937	chr4:20848197-20848198	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs372952530	chr4:20848239-20848240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181421343	chr4:20848288-20848289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79385593	chr4:20848290-20848291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11725280	chr4:20848325-20848326	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs185956380	chr4:20848374-20848375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553482138	chr4:20848417-20848418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572737490	chr4:20848454-20848455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12501882	chr4:20848477-20848478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189164101	chr4:20848479-20848480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576252299	chr4:20848497-20848498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543579052	chr4:20848541-20848542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561858723	chr4:20848542-20848543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546235020	chr4:20848563-20848564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11934232	chr4:20848586-20848587	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs570900216	chr4:20848587-20848588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527617832	chr4:20848598-20848599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552209807	chr4:20848613-20848614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570722807	chr4:20848641-20848642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374574011	chr4:20848684-20848685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531744136	chr4:20848708-20848709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113379083	chr4:20848741-20848742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20834800-20850800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:20842400-20849000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:20846400-20848200	Weak transcription	HMEC	breast
4	chr4:20846400-20848200	Weak transcription	NHEK	skin
5	chr4:20846400-20848400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:20847000-20848200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:20847200-20853400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:20848200-20849600	Enhancers	HMEC	breast
9	chr4:20848200-20849800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:20848200-20849800	Enhancers	NHEK	skin
11	chr4:20848400-20849400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:20849000-20849400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:20853400-20853600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:20853400-20853600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:20853600-20861800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:20855600-20855800	Active TSS	Lung	lung
17	chr4:20855800-20857000	Weak transcription	Lung	lung
18	chr4:20857000-20857200	Enhancers	Lung	lung
19	chr4:20857600-20858600	Enhancers	HUVEC	blood vessel
20	chr4:20858000-20858400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr4:20860200-20860600	Enhancers	HSMMtube	muscle
22	chr4:20860600-20861000	Weak transcription	HSMMtube	muscle
23	chr4:20860600-20862000	Enhancers	NHEK	skin
24	chr4:20860800-20861200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:20861000-20861200	Enhancers	HSMMtube	muscle
26	chr4:20861000-20862800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:20861200-20862000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:20861200-20862400	Weak transcription	HSMMtube	muscle
29	chr4:20861800-20862000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:20862000-20862400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:20862000-20862400	Weak transcription	NHEK	skin
32	chr4:20862000-20862800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:20862400-20862800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:20862400-20862800	Enhancers	NHEK	skin
35	chr4:20862400-20863200	Enhancers	HSMMtube	muscle
36	chr4:20862800-20863200	Enhancers	Placenta Amnion	Placenta Amnion
37	chr4:20871800-20872600	Enhancers	HSMMtube	muscle
38	chr4:20872400-20873200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:20883600-20887000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr4:20883800-20884000	Enhancers	Ovary	ovary
41	chr4:20883800-20884400	Active TSS	Brain Cingulate Gyrus	brain
42	chr4:20884000-20884400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:20884000-20884400	Active TSS	Brain Hippocampus Middle	brain
44	chr4:20884000-20884600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr4:20884000-20884600	Active TSS	Brain Anterior Caudate	brain
46	chr4:20884000-20884600	Active TSS	Ovary	ovary
47	chr4:20884200-20884400	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr4:20887200-20891600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr4:20891400-20891800	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr4:20891600-20892000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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