Variant report

Variant	nsv609010
Chromosome Location	chr7:150706383-150708089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:275)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:275 , 50 per page) page: 1 2 3 4 5 6

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	ATF3	chr7:150706455-150706881	K562	blood:	n/a	n/a
3	BACH1	chr7:150707629-150707768	K562	blood:	n/a	n/a
4	BACH1	chr7:150707503-150707744	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr7:150705149-150706877	K562	blood:	n/a	n/a
6	BHLHE40	chr7:150707405-150708222	K562	blood:	n/a	n/a
7	CBX3	chr7:150707102-150708607	K562	blood:	n/a	n/a
8	CBX3	chr7:150704584-150707060	K562	blood:	n/a	n/a
9	CCNT2	chr7:150706484-150706915	K562	blood:	n/a	n/a
10	CCNT2	chr7:150707232-150707920	K562	blood:	n/a	n/a
11	CEBPD	chr7:150704723-150706889	K562	blood:	n/a	n/a
12	CHD2	chr7:150707587-150707851	HepG2	liver:	n/a	n/a
13	CHD2	chr7:150707494-150707744	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr7:150707013-150707140	K562	blood:	n/a	n/a
15	CHD2	chr7:150705249-150706411	K562	blood:	n/a	chr7:150706263-150706273
16	CHD2	chr7:150707430-150707989	K562	blood:	n/a	n/a
17	CTCF	chr7:150705637-150706837	HCT-116	colon:	n/a	n/a
18	CTCF	chr7:150705686-150706397	K562	blood:	n/a	n/a
19	CTCF	chr7:150706520-150706670	K562	blood:	n/a	n/a
20	CTCF	chr7:150705524-150707108	HCT-116	colon:	n/a	n/a
21	CTCF	chr7:150706520-150706670	AG09319	gingival:	n/a	n/a
22	CTCF	chr7:150706520-150706670	HRE	kidney:	n/a	n/a
23	CTCF	chr7:150706467-150706704	HepG2	liver:	n/a	n/a
24	CTCF	chr7:150706457-150706722	K562	blood:	n/a	n/a
25	CTCF	chr7:150706460-150706610	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:150706365-150706793	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:150706403-150706966	K562	blood:	n/a	n/a
28	CTCF	chr7:150706480-150706630	A549	lung:	n/a	n/a
29	CTCF	chr7:150707660-150707810	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr7:150706540-150706690	HMF	breast:	n/a	n/a
31	CTCF	chr7:150706540-150706690	GM12864	blood:	n/a	n/a
32	CTCF	chr7:150706480-150706630	GM12875	blood:	n/a	n/a
33	CTCF	chr7:150706320-150706470	GM12867	blood:	n/a	n/a
34	CTCF	chr7:150706369-150706806	K562	blood:	n/a	n/a
35	CTCF	chr7:150706575-150706616	GM10248	blood:	n/a	n/a
36	CTCF	chr7:150706580-150706730	GM12874	blood:	n/a	n/a
37	CTCF	chr7:150706540-150706690	GM12873	blood:	n/a	n/a
38	CTCF	chr7:150706480-150706630	GM12872	blood:	n/a	n/a
39	CTCF	chr7:150706580-150706830	AG04449	skin:	n/a	n/a
40	CTCF	chr7:150706530-150706620	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:150706460-150706610	GM12869	blood:	n/a	n/a
42	CTCF	chr7:150706560-150706710	HVMF	connective:	n/a	n/a
43	CTCF	chr7:150706571-150706590	Gliobla	brain:	n/a	n/a
44	CTCF	chr7:150705167-150706983	K562	blood:	n/a	n/a
45	CTCF	chr7:150706540-150706690	GM12878	blood:	n/a	n/a
46	CTCF	chr7:150706460-150706610	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr7:150706500-150706650	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr7:150706540-150706690	GM06990	blood:	n/a	n/a
49	CTCF	chr7:150706532-150706615	NHEK	skin:	n/a	n/a
50	CTCF	chr7:150706480-150706630	HFF-Myc	foreskin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150707830-150707880	ProgFib	skin:	n/a
2	chr7:150707313-150707363	AG09309	skin:	n/a
3	chr7:150707830-150707880	CMK	blood:	n/a
4	chr7:150706355-150706405	AG10803	skin:	n/a
5	chr7:150707830-150707880	AG10803	skin:	n/a
6	chr7:150707313-150707363	HEK293	kidney:	embryo
7	chr7:150707313-150707363	HNPCEpiC	eye:	n/a
8	chr7:150707313-150707363	SK-N-MC	brain:	n/a
9	chr7:150707830-150707880	NH-A	brain:	n/a
10	chr7:150706355-150706405	SAEC	small airway:	n/a
11	chr7:150706355-150706405	AoSMC	blood vessel:	n/a
12	chr7:150707830-150707880	Hepatocyte	liver:	n/a
13	chr7:150706355-150706405	SK-N-SH_RA	brain:	n/a
14	chr7:150707830-150707880	ovcar-3	ovarian:	n/a
15	chr7:150707313-150707363	HRE	kidney:	n/a
16	chr7:150707313-150707363	Hela-S3	cervix:	n/a
17	chr7:150707830-150707880	HepG2	liver:	n/a
18	chr7:150707313-150707363	HMEC	breast:	n/a
19	chr7:150706355-150706405	HNPCEpiC	eye:	n/a
20	chr7:150706355-150706405	H1-hESC	embryonic stem cell:	embryo
21	chr7:150707830-150707880	T-47D	breast:	n/a
22	chr7:150707313-150707363	GM12878	blood:	n/a
23	chr7:150707830-150707880	HRPEpiC	eye:	n/a
24	chr7:150707830-150707880	AG04450	lung:	fetal
25	chr7:150707313-150707363	U87	brain:	n/a
26	chr7:150707830-150707880	IMR90	lung:	fetal
27	chr7:150707313-150707363	LNCaP	prostate:	n/a
28	chr7:150706355-150706405	Jurkat	blood:	n/a
29	chr7:150707830-150707880	RPTEC	kidney:	n/a
30	chr7:150706355-150706405	Hepatocyte	liver:	n/a
31	chr7:150707830-150707880	MCF10A-Er-Src	breast:	n/a
32	chr7:150707830-150707880	HCF	heart:	n/a
33	chr7:150707830-150707880	SK-N-SH_RA	brain:	n/a
34	chr7:150707830-150707880	PrEC	prostate:	n/a
35	chr7:150707313-150707363	ECC-1	luminal epithelium:	n/a
36	chr7:150707313-150707363	NHBE	bronchial:	n/a
37	chr7:150706355-150706405	HCPEpiC	choroid plexus:	n/a
38	chr7:150707313-150707363	HCF	heart:	n/a
39	chr7:150706355-150706405	MCF10A-Er-Src	breast:	n/a
40	chr7:150707830-150707880	HEEpiC	esophagus:	n/a
41	chr7:150707830-150707880	NT2-D1	testis:	n/a
42	chr7:150707830-150707880	NHDF-neo	bronchial:	n/a
43	chr7:150706355-150706405	NHDF-neo	bronchial:	n/a
44	chr7:150707313-150707363	K562	blood:	n/a
45	chr7:150707830-150707880	HIPEpiC	eye:	n/a
46	chr7:150707313-150707363	BJ	skin:	n/a
47	chr7:150706355-150706405	HMEC	breast:	n/a
48	chr7:150706355-150706405	NHBE	bronchial:	n/a
49	chr7:150707313-150707363	AoSMC	blood vessel:	n/a
50	chr7:150707830-150707880	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:150705481..150706887-chr7:150725454..150726471,3	K562	blood:
2	chr7:150705619..150708029-chr7:150714028..150715967,2	MCF-7	breast:
3	chr7:150706188..150708123-chr7:150710621..150712135,2	MCF-7	breast:
4	chr7:150705881..150707323-chr7:150714964..150716387,6	K562	blood:

No data

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

Extended variants
information (count: 98 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:98 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs753482	chr7:150706383-150706384	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142498418	chr7:150706436-150706437	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs137995185	chr7:150706442-150706443	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs527595098	chr7:150706473-150706474	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs200183107	chr7:150706502-150706503	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs536326010	chr7:150706513-150706514	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs56331996	chr7:150706521-150706522	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs368180942	chr7:150706545-150706546	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs200385697	chr7:150706563-150706564	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs137919476	chr7:150706621-150706622	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs538467705	chr7:150706624-150706625	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs558767937	chr7:150706627-150706628	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs3918232	chr7:150706640-150706641	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs199636732	chr7:150706663-150706664	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs371226519	chr7:150706687-150706688	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs3918199	chr7:150706693-150706694	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs369082701	chr7:150706721-150706722	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs554263131	chr7:150706736-150706737	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs3918200	chr7:150706741-150706742	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs540311646	chr7:150706761-150706762	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs560314792	chr7:150706816-150706817	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs569988810	chr7:150706833-150706834	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573430092	chr7:150706849-150706850	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs575623732	chr7:150706881-150706882	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs743506	chr7:150706915-150706916	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs531110178	chr7:150706979-150706980	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs551284888	chr7:150706992-150706993	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561110289	chr7:150706998-150706999	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs530050733	chr7:150707082-150707083	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546660169	chr7:150707090-150707091	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143462889	chr7:150707095-150707096	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs3730009	chr7:150707117-150707118	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs372104569	chr7:150707166-150707167	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200032919	chr7:150707185-150707186	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552075241	chr7:150707192-150707193	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs369652420	chr7:150707227-150707228	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs543098320	chr7:150707243-150707244	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs148919189	chr7:150707251-150707252	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145765422	chr7:150707253-150707254	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs376431860	chr7:150707256-150707257	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs201579252	chr7:150707257-150707258	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs200630478	chr7:150707299-150707300	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs34967063	chr7:150707312-150707313	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs201601172	chr7:150707314-150707315	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs113711626	chr7:150707317-150707318	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200507709	chr7:150707332-150707333	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs3918201	chr7:150707344-150707345	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs142910826	chr7:150707362-150707363	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs199911901	chr7:150707363-150707364	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200006061	chr7:150707392-150707393	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	2 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:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150699800-150706600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:150701000-150706800	Weak transcription	A549	lung
3	chr7:150703600-150708200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr7:150704000-150706600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:150704200-150706400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:150704200-150707200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:150704400-150707200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:150704600-150707000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:150704800-150706400	Enhancers	Primary B cells from cord blood	blood
10	chr7:150704800-150708000	Enhancers	Primary hematopoietic stem cells	blood
11	chr7:150705000-150706400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr7:150705000-150706800	Flanking Active TSS	Dnd41	blood
13	chr7:150705000-150711000	Enhancers	Placenta Amnion	Placenta Amnion
14	chr7:150705200-150706800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:150705200-150708400	Enhancers	Fetal Heart	heart
16	chr7:150705400-150706600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:150705600-150706400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr7:150705600-150706400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:150705600-150708000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:150705800-150706400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:150705800-150706400	Enhancers	HUVEC	blood vessel
22	chr7:150705800-150706600	Flanking Active TSS	HepG2	liver
23	chr7:150705800-150707400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr7:150705800-150707600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr7:150705800-150707600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:150705800-150708200	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr7:150705800-150708400	Enhancers	Fetal Lung	lung
28	chr7:150705800-150710800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:150705800-150711000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr7:150706000-150706400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr7:150706000-150706400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:150706000-150706400	Enhancers	Primary B cells from peripheral blood	blood
33	chr7:150706000-150706400	Bivalent Enhancer	Adipose Nuclei	Adipose
34	chr7:150706000-150706400	Enhancers	Right Ventricle	heart
35	chr7:150706000-150706600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:150706000-150706800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:150706000-150707000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr7:150706000-150707000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:150706000-150707200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:150706000-150707400	Enhancers	Fetal Intestine Large	intestine
41	chr7:150706000-150707400	Weak transcription	Fetal Kidney	kidney
42	chr7:150706000-150707600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:150706000-150707600	Weak transcription	Brain Anterior Caudate	brain
44	chr7:150706000-150707600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr7:150706000-150707600	Enhancers	Fetal Intestine Small	intestine
46	chr7:150706000-150707600	Bivalent Enhancer	Fetal Stomach	stomach
47	chr7:150706000-150707600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr7:150706000-150708000	Weak transcription	Gastric	stomach
49	chr7:150706000-150708200	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr7:150706000-150708200	Bivalent Enhancer	Fetal Thymus	thymus

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