Variant report

Variant	nsv889472
Chromosome Location	chr7:150703414-150707837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:624)
CpG islands
(count:672)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:624 , 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	chr7:150705096-150706111	K562	blood:	n/a	n/a
2	ARID3A	chr7:150707551-150707746	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	chr7:150707629-150707768	K562	blood:	n/a	n/a
7	BACH1	chr7:150705850-150706094	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:150705380-150706071	K562	blood:	n/a	n/a
9	BACH1	chr7:150707503-150707744	H1-hESC	embryonic stem cell:	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	chr7:150705157-150706237	K562	blood:	n/a	n/a
20	CCNT2	chr7:150707232-150707920	K562	blood:	n/a	n/a
21	CCNT2	chr7:150704517-150704594	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	chr7:150705686-150706009	HepG2	liver:	n/a	n/a
27	CEBPD	chr7:150704723-150706889	K562	blood:	n/a	n/a
28	CHD2	chr7:150705249-150706411	K562	blood:	n/a	chr7:150706263-150706273
29	CHD2	chr7:150707013-150707140	K562	blood:	n/a	n/a
30	CHD2	chr7:150707494-150707744	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr7:150706272-150706275	HepG2	liver:	n/a	n/a
32	CHD2	chr7:150705619-150706076	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr7:150707430-150707989	K562	blood:	n/a	n/a
34	CHD2	chr7:150707587-150707851	HepG2	liver:	n/a	n/a
35	CHD2	chr7:150705857-150706057	HepG2	liver:	n/a	n/a
36	CHD2	chr7:150705671-150706146	GM12878	blood:	n/a	n/a
37	CTCF	chr7:150706460-150706610	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr7:150705920-150706070	GM06990	blood:	n/a	n/a
39	CTCF	chr7:150706460-150706610	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr7:150705897-150706077	GM20000	blood:	n/a	n/a
41	CTCF	chr7:150705849-150706118	GM10266	blood:	n/a	n/a
42	CTCF	chr7:150705845-150706131	GM12892	blood:	n/a	n/a
43	CTCF	chr7:150706460-150706610	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr7:150706540-150706690	HepG2	liver:	n/a	n/a
45	CTCF	chr7:150705860-150706010	GM12864	blood:	n/a	n/a
46	CTCF	chr7:150705524-150707108	HCT-116	colon:	n/a	n/a
47	CTCF	chr7:150706386-150706706	HepG2	liver:	n/a	n/a
48	CTCF	chr7:150705920-150706070	BJ	skin:	n/a	n/a
49	CTCF	chr7:150706252-150706356	K562	blood:	n/a	n/a
50	CTCF	chr7:150705834-150706153	HepG2	liver:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150705760-150705810	U87	brain:	n/a
2	chr7:150705760-150705810	U87	brain:	n/a
3	chr7:150706268-150706318	MCF10A-Er-Src	breast:	n/a
4	chr7:150706268-150706318	GM12891	blood:	n/a
5	chr7:150705760-150705810	K562	blood:	n/a
6	chr7:150705000-150705050	RPTEC	kidney:	n/a
7	chr7:150707830-150707880	HCF	heart:	n/a
8	chr7:150706321-150706371	SKMC	muscle:	n/a
9	chr7:150706355-150706405	NHBE	bronchial:	n/a
10	chr7:150707830-150707880	PrEC	prostate:	n/a
11	chr7:150705872-150705922	LNCaP	prostate:	n/a
12	chr7:150706355-150706405	PFSK-1	brain:	n/a
13	chr7:150706128-150706178	A549	lung:	n/a
14	chr7:150707830-150707880	NH-A	brain:	n/a
15	chr7:150706321-150706371	Hela-S3	cervix:	n/a
16	chr7:150706321-150706371	A549	lung:	n/a
17	chr7:150703765-150703815	Caco-2	colon:	n/a
18	chr7:150707313-150707363	GM12892	blood:	n/a
19	chr7:150706128-150706178	CMK	blood:	n/a
20	chr7:150705872-150705922	HEEpiC	esophagus:	n/a
21	chr7:150706321-150706371	SK-N-SH	brain:	n/a
22	chr7:150706128-150706178	U87	brain:	n/a
23	chr7:150705760-150705810	HCT-116	colon:	n/a
24	chr7:150707830-150707880	HAEpiC	amniotic membrane:	n/a
25	chr7:150707313-150707363	CMK	blood:	n/a
26	chr7:150705872-150705922	SAEC	small airway:	n/a
27	chr7:150703765-150703815	GM12892	blood:	n/a
28	chr7:150705896-150705946	HRPEpiC	eye:	n/a
29	chr7:150705872-150705922	HIPEpiC	eye:	n/a
30	chr7:150705872-150705922	SK-N-MC	brain:	n/a
31	chr7:150707830-150707880	RPTEC	kidney:	n/a
32	chr7:150707830-150707880	NHDF-neo	bronchial:	n/a
33	chr7:150706128-150706178	HIPEpiC	eye:	n/a
34	chr7:150706128-150706178	PFSK-1	brain:	n/a
35	chr7:150705872-150705922	Hepatocyte	liver:	n/a
36	chr7:150706321-150706371	Jurkat	blood:	n/a
37	chr7:150706268-150706318	NT2-D1	testis:	n/a
38	chr7:150706321-150706371	HRE	kidney:	n/a
39	chr7:150706321-150706371	GM19239	blood:	n/a
40	chr7:150705872-150705922	SK-N-SH_RA	brain:	n/a
41	chr7:150703765-150703815	HCF	heart:	n/a
42	chr7:150705760-150705810	AoSMC	blood vessel:	n/a
43	chr7:150707313-150707363	IMR90	lung:	fetal
44	chr7:150706128-150706178	SK-N-MC	brain:	n/a
45	chr7:150705000-150705050	HCT-116	colon:	n/a
46	chr7:150705872-150705922	BJ	skin:	n/a
47	chr7:150705000-150705050	A549	lung:	n/a
48	chr7:150705872-150705922	HepG2	liver:	n/a
49	chr7:150705760-150705810	SAEC	small airway:	n/a
50	chr7:150705872-150705922	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:150705881..150707323-chr7:150714964..150716387,6	K562	blood:
2	chr7:150702588..150705432-chr7:150714534..150717607,5	MCF-7	breast:
3	chr7:150706188..150708123-chr7:150710621..150712135,2	MCF-7	breast:
4	chr7:150705481..150706887-chr7:150725454..150726471,3	K562	blood:
5	chr7:150705619..150708029-chr7:150714028..150715967,2	MCF-7	breast:
6	chr1:201951630..201952197-chr7:150703679..150704350,2	HCT-116	colon:
7	chr7:150570280..150573172-chr7:150702825..150704695,2	K562	blood:
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
ENSG00000197150	chromatin interactions
ENSG00000164867	chromatin interactions
ENSG00000181652	chromatin interactions
ENSG00000176393	chromatin interactions

Extended variants
information (count: 228 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:228 , 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	rs2566513	chr7:150703414-150703415	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs189182626	chr7:150703437-150703438	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534758823	chr7:150703497-150703498	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs374477075	chr7:150703509-150703510	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200491007	chr7:150703510-150703511	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs368760176	chr7:150703521-150703522	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs546714296	chr7:150703556-150703557	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs145168353	chr7:150703567-150703568	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs144881606	chr7:150703571-150703572	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs371254663	chr7:150703622-150703623	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs3729625	chr7:150703692-150703693	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs576321738	chr7:150703697-150703698	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs3834873	chr7:150703742-150703743	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs34554797	chr7:150703743-150703744	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs542215416	chr7:150703765-150703766	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs561993605	chr7:150703788-150703789	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs3918191	chr7:150703822-150703823	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
18	rs41408449	chr7:150703876-150703877	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs531235138	chr7:150703887-150703888	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs201547415	chr7:150703890-150703891	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs34372288	chr7:150703892-150703893	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs554105643	chr7:150703900-150703901	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs550073480	chr7:150703907-150703908	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

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:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr7:150697600-150703800	Weak transcription	Primary T cells from cord blood	blood
13	chr7:150697800-150703600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr7:150697800-150704400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr7:150698200-150703800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr7:150698200-150704000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:150698200-150704000	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr7:150698200-150704200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:150698400-150703800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr7:150699000-150703600	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr7:150699200-150704200	Weak transcription	Right Ventricle	heart
22	chr7:150699400-150703600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr7:150699800-150703600	Weak transcription	Lung	lung
24	chr7:150699800-150706600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:150700200-150704000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr7:150700400-150704400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:150700600-150704200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr7:150701000-150704000	Weak transcription	Gastric	stomach
29	chr7:150701000-150704400	Weak transcription	K562	blood
30	chr7:150701000-150704800	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr7:150701000-150706800	Weak transcription	A549	lung
32	chr7:150701400-150703600	Strong transcription	Placenta	Placenta
33	chr7:150702200-150704600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr7:150702600-150703600	Strong transcription	Spleen	Spleen
35	chr7:150703000-150704400	Weak transcription	Adipose Nuclei	Adipose
36	chr7:150703200-150704200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr7:150703400-150704000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr7:150703400-150704400	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr7:150703400-150705200	Flanking Active TSS	HepG2	liver
40	chr7:150703400-150705400	Enhancers	HUVEC	blood vessel
41	chr7:150703400-150705600	Weak transcription	Esophagus	oesophagus
42	chr7:150703600-150704200	Genic enhancers	Spleen	Spleen
43	chr7:150703600-150704400	Genic enhancers	Lung	lung
44	chr7:150703600-150705000	Enhancers	Primary T cells fromperipheralblood	blood
45	chr7:150703600-150705000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr7:150703600-150705400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr7:150703600-150705600	Genic enhancers	Placenta	Placenta
48	chr7:150703600-150708200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr7:150703800-150704000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:150703800-150704000	Enhancers	Brain Cingulate Gyrus	brain

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