Variant report

Variant	nsv609005
Chromosome Location	chr7:150704400-150708035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:630)
CpG islands
(count:611)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:630 , 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	chr7:150705380-150706071	K562	blood:	n/a	n/a
7	BACH1	chr7:150705850-150706094	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:150707629-150707768	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	chr7:150705569-150706124	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:150707405-150708222	K562	blood:	n/a	n/a
13	BHLHE40	chr7:150705149-150706877	K562	blood:	n/a	n/a
14	BHLHE40	chr7:150705759-150706350	HepG2	liver:	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	chr7:150707102-150708607	K562	blood:	n/a	n/a
18	CBX3	chr7:150704584-150707060	K562	blood:	n/a	n/a
19	CCNT2	chr7:150706484-150706915	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	chr7:150704517-150704594	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	chr7:150704723-150706889	K562	blood:	n/a	n/a
26	CEBPD	chr7:150705686-150706009	HepG2	liver:	n/a	n/a
27	CEBPD	chr7:150705057-150706081	K562	blood:	n/a	n/a
28	CHD2	chr7:150705671-150706146	GM12878	blood:	n/a	n/a
29	CHD2	chr7:150707013-150707140	K562	blood:	n/a	n/a
30	CHD2	chr7:150705857-150706057	HepG2	liver:	n/a	n/a
31	CHD2	chr7:150705619-150706076	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr7:150707430-150707989	K562	blood:	n/a	n/a
33	CHD2	chr7:150707587-150707851	HepG2	liver:	n/a	n/a
34	CHD2	chr7:150706272-150706275	HepG2	liver:	n/a	n/a
35	CHD2	chr7:150707494-150707744	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr7:150705249-150706411	K562	blood:	n/a	chr7:150706263-150706273
37	CTCF	chr7:150706220-150706370	HMF	breast:	n/a	n/a
38	CTCF	chr7:150706386-150706706	HepG2	liver:	n/a	n/a
39	CTCF	chr7:150705733-150705762	GM19240	blood:	n/a	n/a
40	CTCF	chr7:150705840-150706122	GM19240	blood:	n/a	n/a
41	CTCF	chr7:150706245-150706286	GM19240	blood:	n/a	n/a
42	CTCF	chr7:150706460-150706610	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr7:150706460-150706610	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr7:150705167-150706983	K562	blood:	n/a	n/a
45	CTCF	chr7:150705880-150706030	NHEK	skin:	n/a	n/a
46	CTCF	chr7:150705900-150706050	GM12878	blood:	n/a	n/a
47	CTCF	chr7:150705800-150705950	A549	lung:	n/a	n/a
48	CTCF	chr7:150705900-150706050	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr7:150705900-150706050	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr7:150705880-150706030	HPF	lung:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150705760-150705810	HepG2	liver:	n/a
2	chr7:150705760-150705810	HepG2	liver:	n/a
3	chr7:150705000-150705050	HMEC	breast:	n/a
4	chr7:150705896-150705946	HUVEC	blood vessel:	n/a
5	chr7:150707830-150707880	Jurkat	blood:	n/a
6	chr7:150706128-150706178	SAEC	small airway:	n/a
7	chr7:150706321-150706371	GM12891	blood:	n/a
8	chr7:150705000-150705050	U87	brain:	n/a
9	chr7:150705896-150705946	RPTEC	kidney:	n/a
10	chr7:150707830-150707880	GM12892	blood:	n/a
11	chr7:150706128-150706178	IMR90	lung:	fetal
12	chr7:150705000-150705050	SKMC	muscle:	n/a
13	chr7:150705896-150705946	NH-A	brain:	n/a
14	chr7:150705000-150705050	HAEpiC	amniotic membrane:	n/a
15	chr7:150705000-150705050	BJ	skin:	n/a
16	chr7:150705896-150705946	AG04449	skin:	fetal
17	chr7:150706355-150706405	HMEC	breast:	n/a
18	chr7:150705872-150705922	GM12892	blood:	n/a
19	chr7:150706321-150706371	HIPEpiC	eye:	n/a
20	chr7:150706321-150706371	SKMC	muscle:	n/a
21	chr7:150706355-150706405	HRE	kidney:	n/a
22	chr7:150706321-150706371	H1-hESC	embryonic stem cell:	embryo
23	chr7:150705896-150705946	AG09309	skin:	n/a
24	chr7:150705896-150705946	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:150706355-150706405	GM12892	blood:	n/a
26	chr7:150705760-150705810	AG04449	skin:	fetal
27	chr7:150707830-150707880	BE2_C	brain:	n/a
28	chr7:150705760-150705810	HNPCEpiC	eye:	n/a
29	chr7:150706321-150706371	NT2-D1	testis:	n/a
30	chr7:150705872-150705922	HNPCEpiC	eye:	n/a
31	chr7:150705872-150705922	AG10803	skin:	n/a
32	chr7:150706128-150706178	U87	brain:	n/a
33	chr7:150706321-150706371	Hela-S3	cervix:	n/a
34	chr7:150706321-150706371	MCF-7	breast:	n/a
35	chr7:150706128-150706178	SK-N-SH	brain:	n/a
36	chr7:150706355-150706405	MCF10A-Er-Src	breast:	n/a
37	chr7:150707313-150707363	GM06990	blood:	n/a
38	chr7:150705872-150705922	A549	lung:	n/a
39	chr7:150705000-150705050	AG04450	lung:	fetal
40	chr7:150705760-150705810	SK-N-MC	brain:	n/a
41	chr7:150706268-150706318	HRCEpiC	kidney:	n/a
42	chr7:150706321-150706371	GM06990	blood:	n/a
43	chr7:150706128-150706178	A549	lung:	n/a
44	chr7:150706128-150706178	SKMC	muscle:	n/a
45	chr7:150705872-150705922	MCF-7	breast:	n/a
46	chr7:150705760-150705810	CMK	blood:	n/a
47	chr7:150706128-150706178	RPTEC	kidney:	n/a
48	chr7:150706268-150706318	IMR90	lung:	fetal
49	chr7:150705000-150705050	ovcar-3	ovarian:	n/a
50	chr7:150707830-150707880	HMEC	breast:	n/a

(count:7 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 186 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:186 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	rs572321236	chr7:150704842-150704843	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs891511	chr7:150704843-150704844	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs573779076	chr7:150704895-150704896	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs184322652	chr7:150704976-150704977	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs10595051	chr7:150704979-150704980	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs559236630	chr7:150705081-150705082	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs528036154	chr7:150705125-150705126	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs370781999	chr7:150705149-150705150	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs544606496	chr7:150705181-150705182	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs3918194	chr7:150705200-150705201	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs541104592	chr7:150705216-150705217	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs143705061	chr7:150705220-150705221	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs116253356	chr7:150705224-150705225	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs552739559	chr7:150705253-150705254	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs550437143	chr7:150705254-150705255	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs570209659	chr7:150705285-150705286	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs372949401	chr7:150705320-150705321	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs112201945	chr7:150705325-150705326	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs549619734	chr7:150705337-150705338	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs566387255	chr7:150705381-150705382	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs3918230	chr7:150705413-150705414	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369935793	chr7:150705425-150705426	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs3918195	chr7:150705444-150705445	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs189069620	chr7:150705500-150705501	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs558182681	chr7:150705535-150705536	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs554255447	chr7:150705536-150705537	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs537527217	chr7:150705546-150705547	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs557194282	chr7:150705595-150705596	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs1008140	chr7:150705610-150705611	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs146829069	chr7:150705618-150705619	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs552799938	chr7:150705634-150705635	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	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:438 , 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	chr7:150692400-150704400	Weak transcription	Right Atrium	heart
3	chr7:150694400-150704400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr7:150694600-150705600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:150694800-150704800	Weak transcription	Fetal Lung	lung
6	chr7:150694800-150705200	Weak transcription	Fetal Intestine Small	intestine
7	chr7:150695000-150705400	Weak transcription	Fetal Intestine Large	intestine
8	chr7:150695600-150704600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr7:150697800-150704400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr7:150699800-150706600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:150700400-150704400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:150701000-150704400	Weak transcription	K562	blood
13	chr7:150701000-150704800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr7:150701000-150706800	Weak transcription	A549	lung
15	chr7:150702200-150704600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr7:150703000-150704400	Weak transcription	Adipose Nuclei	Adipose
17	chr7:150703400-150704400	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr7:150703400-150705200	Flanking Active TSS	HepG2	liver
19	chr7:150703400-150705400	Enhancers	HUVEC	blood vessel
20	chr7:150703400-150705600	Weak transcription	Esophagus	oesophagus
21	chr7:150703600-150704400	Genic enhancers	Lung	lung
22	chr7:150703600-150705000	Enhancers	Primary T cells fromperipheralblood	blood
23	chr7:150703600-150705000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:150703600-150705400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:150703600-150705600	Genic enhancers	Placenta	Placenta
26	chr7:150703600-150708200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr7:150703800-150704800	Enhancers	Primary T cells from cord blood	blood
28	chr7:150703800-150705000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr7:150703800-150705000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr7:150703800-150705200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr7:150703800-150705400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr7:150704000-150704600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr7:150704000-150704600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr7:150704000-150704600	Active TSS	Gastric	stomach
35	chr7:150704000-150704800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr7:150704000-150704800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr7:150704000-150705200	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr7:150704000-150705400	Enhancers	Fetal Muscle Leg	muscle
39	chr7:150704000-150706000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:150704000-150706000	Enhancers	Left Ventricle	heart
41	chr7:150704000-150706600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:150704200-150704400	Enhancers	Liver	Liver
43	chr7:150704200-150704400	Enhancers	Duodenum Mucosa	Duodenum
44	chr7:150704200-150705000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr7:150704200-150705000	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr7:150704200-150705000	Enhancers	Stomach Smooth Muscle	stomach
47	chr7:150704200-150705600	Enhancers	Right Ventricle	heart
48	chr7:150704200-150706000	Enhancers	Spleen	Spleen
49	chr7:150704200-150706400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:150704200-150707200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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