Variant report

Variant	nsv609004
Chromosome Location	chr7:150703915-150708089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:631)
CpG islands
(count:610)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150707551-150707746	K562	blood:	n/a	n/a
2	ARID3A	chr7:150705096-150706111	K562	blood:	n/a	n/a
3	ATF1	chr7:150705143-150706133	K562	blood:	n/a	n/a
4	ATF2	chr7:150705746-150706227	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr7:150706455-150706881	K562	blood:	n/a	n/a
6	BACH1	chr7:150705850-150706094	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:150707503-150707744	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:150707629-150707768	K562	blood:	n/a	n/a
9	BACH1	chr7:150705380-150706071	K562	blood:	n/a	n/a
10	BCLAF1	chr7:150705267-150706200	K562	blood:	n/a	n/a
11	BHLHE40	chr7:150705759-150706350	HepG2	liver:	n/a	n/a
12	BHLHE40	chr7:150707405-150708222	K562	blood:	n/a	n/a
13	BHLHE40	chr7:150705569-150706124	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:150705149-150706877	K562	blood:	n/a	n/a
15	BRCA1	chr7:150705614-150706020	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr7:150705114-150706132	K562	blood:	n/a	n/a
17	CBX3	chr7:150704584-150707060	K562	blood:	n/a	n/a
18	CBX3	chr7:150707102-150708607	K562	blood:	n/a	n/a
19	CCNT2	chr7:150704517-150704594	K562	blood:	n/a	n/a
20	CCNT2	chr7:150707232-150707920	K562	blood:	n/a	n/a
21	CCNT2	chr7:150705157-150706237	K562	blood:	n/a	n/a
22	CCNT2	chr7:150706484-150706915	K562	blood:	n/a	n/a
23	CEBPB	chr7:150705042-150706070	K562	blood:	n/a	chr7:150705403-150705411
24	CEBPB	chr7:150705104-150706135	K562	blood:	n/a	chr7:150705403-150705411
25	CEBPD	chr7:150705057-150706081	K562	blood:	n/a	n/a
26	CEBPD	chr7:150704723-150706889	K562	blood:	n/a	n/a
27	CEBPD	chr7:150705686-150706009	HepG2	liver:	n/a	n/a
28	CHD2	chr7:150705671-150706146	GM12878	blood:	n/a	n/a
29	CHD2	chr7:150707587-150707851	HepG2	liver:	n/a	n/a
30	CHD2	chr7:150705249-150706411	K562	blood:	n/a	chr7:150706263-150706273
31	CHD2	chr7:150706272-150706275	HepG2	liver:	n/a	n/a
32	CHD2	chr7:150705857-150706057	HepG2	liver:	n/a	n/a
33	CHD2	chr7:150705619-150706076	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr7:150707430-150707989	K562	blood:	n/a	n/a
35	CHD2	chr7:150707494-150707744	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr7:150707013-150707140	K562	blood:	n/a	n/a
37	CTCF	chr7:150705940-150706090	NHEK	skin:	n/a	n/a
38	CTCF	chr7:150705900-150706050	GM12867	blood:	n/a	n/a
39	CTCF	chr7:150705900-150706050	HPF	lung:	n/a	n/a
40	CTCF	chr7:150705882-150706070	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr7:150705824-150706102	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:150705960-150706110	HVMF	connective:	n/a	n/a
43	CTCF	chr7:150706530-150706620	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:150705524-150707108	HCT-116	colon:	n/a	n/a
45	CTCF	chr7:150706461-150706718	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr7:150705920-150706070	GM12872	blood:	n/a	n/a
47	CTCF	chr7:150706520-150706670	AG09319	gingival:	n/a	n/a
48	CTCF	chr7:150706560-150706710	HVMF	connective:	n/a	n/a
49	CTCF	chr7:150705828-150706144	GM12878	blood:	n/a	n/a
50	CTCF	chr7:150705920-150706070	HBMEC	blood vessel:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150705000-150705050	SKMC	muscle:	n/a
2	chr7:150706268-150706318	GM19239	blood:	n/a
3	chr7:150706321-150706371	HRPEpiC	eye:	n/a
4	chr7:150705872-150705922	A549	lung:	n/a
5	chr7:150705872-150705922	HEEpiC	esophagus:	n/a
6	chr7:150705872-150705922	AG04449	skin:	fetal
7	chr7:150705000-150705050	K562	blood:	n/a
8	chr7:150705872-150705922	SK-N-SH_RA	brain:	n/a
9	chr7:150706128-150706178	AG04450	lung:	fetal
10	chr7:150706321-150706371	HAEpiC	amniotic membrane:	n/a
11	chr7:150707313-150707363	HepG2	liver:	n/a
12	chr7:150707313-150707363	ECC-1	luminal epithelium:	n/a
13	chr7:150706321-150706371	HEK293	kidney:	embryo
14	chr7:150707313-150707363	AG10803	skin:	n/a
15	chr7:150706321-150706371	AG09319	gingival:	n/a
16	chr7:150707313-150707363	HEK293	kidney:	embryo
17	chr7:150706355-150706405	GM06990	blood:	n/a
18	chr7:150706321-150706371	T-47D	breast:	n/a
19	chr7:150707313-150707363	GM06990	blood:	n/a
20	chr7:150706355-150706405	HEEpiC	esophagus:	n/a
21	chr7:150707313-150707363	NH-A	brain:	n/a
22	chr7:150705760-150705810	GM19239	blood:	n/a
23	chr7:150707313-150707363	BJ	skin:	n/a
24	chr7:150705000-150705050	BJ	skin:	n/a
25	chr7:150705872-150705922	PFSK-1	brain:	n/a
26	chr7:150707313-150707363	HUVEC	blood vessel:	n/a
27	chr7:150706268-150706318	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:150705000-150705050	MCF10A-Er-Src	breast:	n/a
29	chr7:150706355-150706405	SKMC	muscle:	n/a
30	chr7:150707313-150707363	NHDF-neo	bronchial:	n/a
31	chr7:150705896-150705946	GM06990	blood:	n/a
32	chr7:150705000-150705050	HCF	heart:	n/a
33	chr7:150705896-150705946	HRE	kidney:	n/a
34	chr7:150705760-150705810	Hepatocyte	liver:	n/a
35	chr7:150706355-150706405	HRE	kidney:	n/a
36	chr7:150707830-150707880	CMK	blood:	n/a
37	chr7:150706321-150706371	BJ	skin:	n/a
38	chr7:150707313-150707363	HPAEpiC	pulmonary alveolar:	n/a
39	chr7:150706268-150706318	AoSMC	blood vessel:	n/a
40	chr7:150705896-150705946	ovcar-3	ovarian:	n/a
41	chr7:150706321-150706371	HRCEpiC	kidney:	n/a
42	chr7:150706128-150706178	PFSK-1	brain:	n/a
43	chr7:150705760-150705810	SK-N-MC	brain:	n/a
44	chr7:150705872-150705922	HCF	heart:	n/a
45	chr7:150707313-150707363	HCF	heart:	n/a
46	chr7:150707830-150707880	HCT-116	colon:	n/a
47	chr7:150706321-150706371	IMR90	lung:	fetal
48	chr7:150705896-150705946	BE2_C	brain:	n/a
49	chr7:150706268-150706318	SK-N-SH_RA	brain:	n/a
50	chr7:150706321-150706371	HCM	heart:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:201951630..201952197-chr7:150703679..150704350,2	HCT-116	colon:
2	chr7:150705881..150707323-chr7:150714964..150716387,6	K562	blood:
3	chr7:150702588..150705432-chr7:150714534..150717607,5	MCF-7	breast:
4	chr7:150570280..150573172-chr7:150702825..150704695,2	K562	blood:
5	chr7:150706188..150708123-chr7:150710621..150712135,2	MCF-7	breast:
6	chr7:150705481..150706887-chr7:150725454..150726471,3	K562	blood:
7	chr7:150705619..150708029-chr7:150714028..150715967,2	MCF-7	breast:
8	chr7:150703619..150706319-chr7:150708116..150709799,2	MCF-7	breast:

No data

Variant related genes	Relation type
NOS3	TF binding region
NOS3	CpG island
ENSG00000164867	chromatin interactions
ENSG00000197150	chromatin interactions
ENSG00000181652	chromatin interactions
ENSG00000176393	chromatin interactions

Extended variants
information (count: 223 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:223 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2853796	chr7:150703915-150703916	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528845460	chr7:150703919-150703920	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs3918192	chr7:150703928-150703929	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs565589518	chr7:150703929-150703930	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs534395469	chr7:150703933-150703934	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs368037419	chr7:150703962-150703963	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs551086550	chr7:150703987-150703988	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs570681394	chr7:150704038-150704039	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs371971953	chr7:150704039-150704040	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs199798957	chr7:150704046-150704047	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs556539002	chr7:150704083-150704084	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs111855806	chr7:150704114-150704115	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs547152209	chr7:150704122-150704123	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs375280032	chr7:150704127-150704128	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs369496580	chr7:150704142-150704143	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs372459358	chr7:150704146-150704147	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs377209786	chr7:150704173-150704174	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs555722886	chr7:150704174-150704175	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs148623908	chr7:150704202-150704203	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs201515167	chr7:150704208-150704209	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs370017827	chr7:150704235-150704236	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs7792133	chr7:150704246-150704247	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs2566514	chr7:150704250-150704251	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs140717927	chr7:150704277-150704278	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs200567165	chr7:150704319-150704320	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs144370730	chr7:150704337-150704338	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs372783097	chr7:150704339-150704340	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs563391462	chr7:150704359-150704360	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs529187927	chr7:150704372-150704373	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs375508543	chr7:150704386-150704387	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs368899020	chr7:150704388-150704389	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs3730305	chr7:150704400-150704401	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs558899370	chr7:150704401-150704402	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs374893931	chr7:150704406-150704407	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs193112107	chr7:150704431-150704432	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs184329901	chr7:150704446-150704447	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs3918193	chr7:150704479-150704480	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs571017146	chr7:150704499-150704500	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs189178052	chr7:150704545-150704546	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs550345584	chr7:150704559-150704560	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs75594757	chr7:150704651-150704652	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs146553236	chr7:150704687-150704688	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs555815111	chr7:150704785-150704786	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs572444319	chr7:150704790-150704791	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs35771718	chr7:150704805-150704806	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs535033419	chr7:150704806-150704807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs558244120	chr7:150704824-150704825	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs559320581	chr7:150704835-150704836	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs181122640	chr7:150704837-150704838	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs3828997	chr7:150704838-150704839	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150692200-150705000	Weak transcription	Ovary	ovary
2	chr7:150692400-150704200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:150692400-150704400	Weak transcription	Right Atrium	heart
4	chr7:150692600-150704000	Weak transcription	Left Ventricle	heart
5	chr7:150694400-150704400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:150694600-150705600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:150694800-150704800	Weak transcription	Fetal Lung	lung
8	chr7:150694800-150705200	Weak transcription	Fetal Intestine Small	intestine
9	chr7:150695000-150705400	Weak transcription	Fetal Intestine Large	intestine
10	chr7:150695600-150704600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr7:150697000-150704000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr7:150697800-150704400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr7:150698200-150704000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:150698200-150704000	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr7:150698200-150704200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:150699200-150704200	Weak transcription	Right Ventricle	heart
17	chr7:150699800-150706600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:150700200-150704000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr7:150700400-150704400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:150700600-150704200	Weak transcription	Stomach Smooth Muscle	stomach
21	chr7:150701000-150704000	Weak transcription	Gastric	stomach
22	chr7:150701000-150704400	Weak transcription	K562	blood
23	chr7:150701000-150704800	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr7:150701000-150706800	Weak transcription	A549	lung
25	chr7:150702200-150704600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr7:150703000-150704400	Weak transcription	Adipose Nuclei	Adipose
27	chr7:150703200-150704200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr7:150703400-150704000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:150703400-150704400	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr7:150703400-150705200	Flanking Active TSS	HepG2	liver
31	chr7:150703400-150705400	Enhancers	HUVEC	blood vessel
32	chr7:150703400-150705600	Weak transcription	Esophagus	oesophagus
33	chr7:150703600-150704200	Genic enhancers	Spleen	Spleen
34	chr7:150703600-150704400	Genic enhancers	Lung	lung
35	chr7:150703600-150705000	Enhancers	Primary T cells fromperipheralblood	blood
36	chr7:150703600-150705000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr7:150703600-150705400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:150703600-150705600	Genic enhancers	Placenta	Placenta
39	chr7:150703600-150708200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr7:150703800-150704000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:150703800-150704000	Enhancers	Brain Cingulate Gyrus	brain
42	chr7:150703800-150704800	Enhancers	Primary T cells from cord blood	blood
43	chr7:150703800-150705000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr7:150703800-150705000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr7:150703800-150705200	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr7:150703800-150705400	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr7:150704000-150704600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr7:150704000-150704600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr7:150704000-150704600	Active TSS	Gastric	stomach
50	chr7:150704000-150704800	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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