Variant report

Variant	nsv887460
Chromosome Location	chr7:6832265-6952350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1256)
CpG islands
(count:3487)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:6897551-6897628	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr7:6897373-6897774	GM12878	blood:	n/a	n/a
3	BATF	chr7:6930048-6930266	GM12878	blood:	n/a	chr7:6930144-6930155
4	BATF	chr7:6882514-6882830	GM12878	blood:	n/a	n/a
5	BATF	chr7:6865157-6865489	GM12878	blood:	n/a	n/a
6	BATF	chr7:6911365-6911638	GM12878	blood:	n/a	n/a
7	BATF	chr7:6911459-6911623	GM12878	blood:	n/a	n/a
8	BATF	chr7:6865860-6866054	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:6865814-6866066	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:6897283-6897636	GM12878	blood:	n/a	chr7:6897421-6897434
11	BCL3	chr7:6928637-6929472	GM12878	blood:	n/a	n/a
12	BCL3	chr7:6873151-6873685	GM12878	blood:	n/a	n/a
13	BCL3	chr7:6916434-6916785	GM12878	blood:	n/a	n/a
14	BCL3	chr7:6928564-6929398	GM12878	blood:	n/a	n/a
15	BCL3	chr7:6870972-6871253	GM12878	blood:	n/a	n/a
16	BCL3	chr7:6872794-6873775	GM12878	blood:	n/a	n/a
17	BCLAF1	chr7:6897456-6897677	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:6943039-6943099	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:6897488-6897590	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:6832136-6832415	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:6929175-6929309	K562	blood:	n/a	n/a
22	BHLHE40	chr7:6832293-6832495	HepG2	liver:	n/a	n/a
23	BHLHE40	chr7:6865906-6866108	K562	blood:	n/a	n/a
24	BHLHE40	chr7:6865917-6866116	GM12878	blood:	n/a	n/a
25	CBX3	chr7:6864785-6865473	K562	blood:	n/a	n/a
26	CBX3	chr7:6865752-6866597	K562	blood:	n/a	n/a
27	CBX3	chr7:6865692-6866336	K562	blood:	n/a	n/a
28	CBX3	chr7:6866895-6867260	K562	blood:	n/a	n/a
29	CBX3	chr7:6940710-6940918	K562	blood:	n/a	n/a
30	CEBPB	chr7:6935911-6936099	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:6914862-6914979	K562	blood:	n/a	n/a
32	CEBPB	chr7:6936027-6936120	K562	blood:	n/a	n/a
33	CEBPB	chr7:6936030-6936175	A549	lung:	n/a	n/a
34	CEBPB	chr7:6912527-6912646	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:6880359-6880521	K562	blood:	n/a	n/a
36	CEBPB	chr7:6861480-6861661	IMR90	lung:	n/a	chr7:6861544-6861553 chr7:6861542-6861553
37	CEBPB	chr7:6893270-6893470	HepG2	liver:	n/a	chr7:6893406-6893419
38	CHD2	chr7:6865919-6865948	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr7:6897423-6897604	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr7:6865918-6866124	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr7:6865823-6866000	GM12878	blood:	n/a	n/a
42	CHD2	chr7:6866860-6867202	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr7:6865856-6866080	A549	lung:	n/a	n/a
44	CREB1	chr7:6865815-6866098	A549	lung:	n/a	n/a
45	CTCF	chr7:6864886-6864996	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:6897407-6897675	GM19239	blood:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
47	CTCF	chr7:6897480-6897630	AG04449	skin:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
48	CTCF	chr7:6897417-6897621	HepG2	liver:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537
49	CTCF	chr7:6895560-6895710	HCPEpiC	choroid plexus:	n/a	chr7:6895584-6895602 chr7:6895586-6895599
50	CTCF	chr7:6897315-6897632	A549	lung:	n/a	chr7:6897522-6897540 chr7:6897525-6897535 chr7:6897517-6897538 chr7:6897524-6897537 chr7:6897528-6897537

(count:3487 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6894477-6894527	PFSK-1	brain:	n/a
2	chr7:6867070-6867120	GM12891	blood:	n/a
3	chr7:6887294-6887344	PrEC	prostate:	n/a
4	chr7:6892885-6892935	GM06990	blood:	n/a
5	chr7:6867070-6867120	NHDF-neo	bronchial:	n/a
6	chr7:6867074-6867124	AG09319	gingival:	n/a
7	chr7:6864491-6864541	HRE	kidney:	n/a
8	chr7:6911051-6911101	HNPCEpiC	eye:	n/a
9	chr7:6887532-6887582	HRPEpiC	eye:	n/a
10	chr7:6914289-6914339	GM06990	blood:	n/a
11	chr7:6894477-6894527	PFSK-1	brain:	n/a
12	chr7:6867070-6867120	GM12891	blood:	n/a
13	chr7:6887294-6887344	PrEC	prostate:	n/a
14	chr7:6892885-6892935	GM06990	blood:	n/a
15	chr7:6867070-6867120	NHDF-neo	bronchial:	n/a
16	chr7:6867074-6867124	AG09319	gingival:	n/a
17	chr7:6864491-6864541	HRE	kidney:	n/a
18	chr7:6911051-6911101	HNPCEpiC	eye:	n/a
19	chr7:6887532-6887582	HRPEpiC	eye:	n/a
20	chr7:6914289-6914339	GM06990	blood:	n/a
21	chr7:6884098-6884148	ECC-1	luminal epithelium:	n/a
22	chr7:6866040-6866090	T-47D	breast:	n/a
23	chr7:6888133-6888183	A549	lung:	n/a
24	chr7:6836436-6836486	SAEC	small airway:	n/a
25	chr7:6887532-6887582	RPTEC	kidney:	n/a
26	chr7:6909188-6909238	HL-60	blood:	n/a
27	chr7:6915894-6915944	SK-N-SH_RA	brain:	n/a
28	chr7:6886021-6886071	GM12892	blood:	n/a
29	chr7:6887532-6887582	K562	blood:	n/a
30	chr7:6897353-6897403	PANC-1	pancreas:	n/a
31	chr7:6914289-6914339	AoSMC	blood vessel:	n/a
32	chr7:6889162-6889212	HCM	heart:	n/a
33	chr7:6885838-6885888	BJ	skin:	n/a
34	chr7:6885918-6885968	U87	brain:	n/a
35	chr7:6882194-6882244	AG04449	skin:	fetal
36	chr7:6892980-6893030	NT2-D1	testis:	n/a
37	chr7:6910871-6910921	K562	blood:	n/a
38	chr7:6893572-6893622	HAEpiC	amniotic membrane:	n/a
39	chr7:6892911-6892961	Caco-2	colon:	n/a
40	chr7:6864491-6864541	PrEC	prostate:	n/a
41	chr7:6865960-6866010	HCT-116	colon:	n/a
42	chr7:6885838-6885888	HUVEC	blood vessel:	n/a
43	chr7:6885838-6885888	AG09319	gingival:	n/a
44	chr7:6865970-6866020	Hela-S3	cervix:	n/a
45	chr7:6911211-6911261	HepG2	liver:	n/a
46	chr7:6909121-6909171	IMR90	lung:	fetal
47	chr7:6889162-6889212	SK-N-SH_RA	brain:	n/a
48	chr7:6882194-6882244	ProgFib	skin:	n/a
49	chr7:6838775-6838825	Jurkat	blood:	n/a
50	chr7:6886759-6886809	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:6628333..6631201-chr7:6866874..6868650,2	MCF-7	breast:
2	chr7:6629513..6630064-chr7:6897112..6897752,3	MCF-7	breast:
3	chr7:6865395..6868378-chr7:6875321..6876917,2	MCF-7	breast:
4	chr7:6487483..6489084-chr7:6871444..6873922,2	MCF-7	breast:
5	chr7:6865923..6867484-chr7:6871034..6873441,2	MCF-7	breast:
6	chr7:6865395..6868378-chr7:6875321..6876917,2	MCF-7	breast:
7	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCZ1B-1	chr7:6836407-6836567	NONHSAT119073
2	lnc-CCZ1B-1	chr7:6836264-6836309	NONHSAT119073
3	lnc-CCZ1B-1	chr7:6833772-6834166	NONHSAT119073

No data

Variant related genes	Relation type
CCZ1B	TF binding region
ENSG00000243531	TF binding region
UNC93B2	TF binding region
OR7E136P	TF binding region
ENSG00000263457	TF binding region
OR7E59P	TF binding region
OR7E39P	TF binding region
CCZ1B	CpG island
ENSG00000243531	CpG island
UNC93B2	CpG island
OR7E136P	CpG island
ENSG00000263457	CpG island
OR7E59P	CpG island
OR7E39P	CpG island
ENSG00000273252	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000146574	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000187953	chromatin interactions

Extended variants
information (count: 5927 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5927 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79201680	chr7:6832265-6832266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181059977	chr7:6832320-6832321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186196152	chr7:6832335-6832336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556015709	chr7:6832414-6832415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150932403	chr7:6832452-6832453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375402163	chr7:6832585-6832586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs3109231	chr7:6832647-6832648	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs2952951	chr7:6832657-6832658	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs373334434	chr7:6832680-6832681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113202999	chr7:6832700-6832701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200294274	chr7:6832846-6832847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373366961	chr7:6832849-6832850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185927655	chr7:6832913-6832914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190634223	chr7:6832937-6832938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535200909	chr7:6832938-6832939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183161656	chr7:6832948-6832949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189242403	chr7:6832972-6832973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527390670	chr7:6832975-6832976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545061249	chr7:6832982-6832983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200280892	chr7:6832999-6833000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60931010	chr7:6833001-6833002	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs372707682	chr7:6833005-6833006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59137167	chr7:6833020-6833021	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs59435767	chr7:6833047-6833048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557076988	chr7:6833050-6833051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs57876798	chr7:6833051-6833052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs60485381	chr7:6833059-6833060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs58458056	chr7:6833067-6833068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542687480	chr7:6833083-6833084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199777978	chr7:6833135-6833136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561991361	chr7:6833256-6833257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529147062	chr7:6833451-6833452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567734579	chr7:6833452-6833453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199673223	chr7:6833453-6833454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189750378	chr7:6833480-6833481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs397759478	chr7:6833485-6833486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10265755	chr7:6833516-6833517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368719690	chr7:6833601-6833602	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371843722	chr7:6833642-6833643	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs60484709	chr7:6833683-6833684	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs28505617	chr7:6833705-6833706	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113916727	chr7:6833720-6833721	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10266030	chr7:6833724-6833725	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs28431019	chr7:6833747-6833748	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10225697	chr7:6833748-6833749	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559547837	chr7:6833754-6833755	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs28626032	chr7:6833765-6833766	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs28651342	chr7:6833773-6833774	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs149991741	chr7:6833792-6833793	ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs551499600	chr7:6833825-6833826	ZNF genes & repeats Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1087 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6824000-6851600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:6831400-6832400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr7:6831400-6832800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:6831400-6833600	Weak transcription	Primary B cells from peripheral blood	blood
5	chr7:6831400-6848800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:6831400-6849000	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:6831400-6850000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr7:6831400-6850600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:6831400-6856600	Weak transcription	Thymus	Thymus
10	chr7:6832000-6849000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:6832000-6849000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr7:6832000-6850200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:6832000-6850600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:6832000-6851800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr7:6832000-6851800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr7:6832000-6852800	Weak transcription	Brain Germinal Matrix	brain
17	chr7:6832000-6853000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:6832000-6855000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:6832000-6856000	Weak transcription	Fetal Brain Female	brain
20	chr7:6832000-6856400	Weak transcription	Fetal Intestine Large	intestine
21	chr7:6832000-6864600	Weak transcription	Primary T cells from cord blood	blood
22	chr7:6832000-6864800	Weak transcription	Fetal Thymus	thymus
23	chr7:6832200-6832600	Enhancers	Fetal Muscle Leg	muscle
24	chr7:6832200-6832600	Enhancers	HUVEC	blood vessel
25	chr7:6832200-6833600	Weak transcription	Fetal Stomach	stomach
26	chr7:6832200-6849000	Weak transcription	Liver	Liver
27	chr7:6832200-6849800	Weak transcription	Fetal Muscle Trunk	muscle
28	chr7:6832200-6852600	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr7:6832200-6853000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr7:6832200-6860800	Weak transcription	Brain Anterior Caudate	brain
31	chr7:6832400-6832600	Enhancers	NHLF	lung
32	chr7:6832400-6834000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr7:6832400-6850600	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr7:6832400-6850600	Weak transcription	Fetal Intestine Small	intestine
35	chr7:6832400-6856600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr7:6832400-6864600	Weak transcription	Fetal Lung	lung
37	chr7:6832600-6833600	Weak transcription	Fetal Muscle Leg	muscle
38	chr7:6832600-6851800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr7:6832600-6858000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr7:6832600-6861000	Weak transcription	HUVEC	blood vessel
41	chr7:6832600-6864600	Weak transcription	NHLF	lung
42	chr7:6832800-6833000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr7:6832800-6833000	Enhancers	Ovary	ovary
44	chr7:6832800-6833000	Enhancers	Pancreas	Pancrea
45	chr7:6832800-6833600	Weak transcription	Adipose Nuclei	Adipose
46	chr7:6832800-6849400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:6832800-6853000	Weak transcription	Placenta	Placenta
48	chr7:6833000-6833600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr7:6833000-6849800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr7:6833000-6865200	Weak transcription	Left Ventricle	heart

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