Variant report

Variant	nsv887462
Chromosome Location	chr7:6855510-6986809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1861)
CpG islands
(count:3725)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1861 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:6962881-6963081	K562	blood:	n/a	n/a
2	BACH1	chr7:6897551-6897628	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:6959520-6959921	GM12878	blood:	n/a	chr7:6959720-6959731
4	BATF	chr7:6967256-6967613	GM12878	blood:	n/a	n/a
5	BATF	chr7:6970367-6970679	GM12878	blood:	n/a	n/a
6	BATF	chr7:6965792-6966222	GM12878	blood:	n/a	n/a
7	BATF	chr7:6930048-6930266	GM12878	blood:	n/a	chr7:6930144-6930155
8	BATF	chr7:6911459-6911623	GM12878	blood:	n/a	n/a
9	BATF	chr7:6959640-6959863	GM12878	blood:	n/a	chr7:6959720-6959731
10	BATF	chr7:6911365-6911638	GM12878	blood:	n/a	n/a
11	BATF	chr7:6897373-6897774	GM12878	blood:	n/a	n/a
12	BATF	chr7:6967768-6968127	GM12878	blood:	n/a	n/a
13	BATF	chr7:6865860-6866054	GM12878	blood:	n/a	n/a
14	BATF	chr7:6965828-6966219	GM12878	blood:	n/a	n/a
15	BATF	chr7:6865157-6865489	GM12878	blood:	n/a	n/a
16	BATF	chr7:6882514-6882830	GM12878	blood:	n/a	n/a
17	BATF	chr7:6967778-6968070	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:6967281-6967607	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:6966697-6966858	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:6897283-6897636	GM12878	blood:	n/a	chr7:6897421-6897434
21	BCL11A	chr7:6865814-6866066	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:6967360-6967540	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:6965764-6966259	GM12878	blood:	n/a	chr7:6966028-6966037
24	BCL11A	chr7:6968204-6968549	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:6965815-6966145	GM12878	blood:	n/a	chr7:6966028-6966037
26	BCL11A	chr7:6970443-6970693	GM12878	blood:	n/a	n/a
27	BCL3	chr7:6873151-6873685	GM12878	blood:	n/a	n/a
28	BCL3	chr7:6872794-6873775	GM12878	blood:	n/a	n/a
29	BCL3	chr7:6928637-6929472	GM12878	blood:	n/a	n/a
30	BCL3	chr7:6928564-6929398	GM12878	blood:	n/a	n/a
31	BCL3	chr7:6916434-6916785	GM12878	blood:	n/a	n/a
32	BCL3	chr7:6870972-6871253	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:6897456-6897677	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:6962913-6963006	K562	blood:	n/a	n/a
35	BHLHE40	chr7:6929175-6929309	K562	blood:	n/a	n/a
36	BHLHE40	chr7:6865906-6866108	K562	blood:	n/a	n/a
37	BHLHE40	chr7:6968034-6968094	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:6865917-6866116	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:6897488-6897590	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:6943039-6943099	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:6967280-6967585	GM12878	blood:	n/a	n/a
42	CBX3	chr7:6962801-6963079	K562	blood:	n/a	n/a
43	CBX3	chr7:6940710-6940918	K562	blood:	n/a	n/a
44	CBX3	chr7:6865692-6866336	K562	blood:	n/a	n/a
45	CBX3	chr7:6977915-6978267	K562	blood:	n/a	n/a
46	CBX3	chr7:6865752-6866597	K562	blood:	n/a	n/a
47	CBX3	chr7:6864785-6865473	K562	blood:	n/a	n/a
48	CBX3	chr7:6962809-6962993	K562	blood:	n/a	n/a
49	CBX3	chr7:6866895-6867260	K562	blood:	n/a	n/a
50	CBX3	chr7:6965814-6966339	K562	blood:	n/a	n/a

(count:3725 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6886759-6886809	ovcar-3	ovarian:	n/a
2	chr7:6974892-6974942	AG04450	lung:	fetal
3	chr7:6889129-6889179	SK-N-MC	brain:	n/a
4	chr7:6889162-6889212	GM19239	blood:	n/a
5	chr7:6886759-6886809	ovcar-3	ovarian:	n/a
6	chr7:6974892-6974942	AG04450	lung:	fetal
7	chr7:6889129-6889179	SK-N-MC	brain:	n/a
8	chr7:6889162-6889212	GM19239	blood:	n/a
9	chr7:6915373-6915423	SKMC	muscle:	n/a
10	chr7:6885539-6885589	GM19239	blood:	n/a
11	chr7:6921561-6921611	PrEC	prostate:	n/a
12	chr7:6915894-6915944	HL-60	blood:	n/a
13	chr7:6867074-6867124	SKMC	muscle:	n/a
14	chr7:6979239-6979289	NHDF-neo	bronchial:	n/a
15	chr7:6888415-6888465	HCM	heart:	n/a
16	chr7:6897353-6897403	NB4	blood:	n/a
17	chr7:6911051-6911101	HCPEpiC	choroid plexus:	n/a
18	chr7:6886021-6886071	BE2_C	brain:	n/a
19	chr7:6916089-6916139	MCF10A-Er-Src	breast:	n/a
20	chr7:6915508-6915558	NHDF-neo	bronchial:	n/a
21	chr7:6893572-6893622	ovcar-3	ovarian:	n/a
22	chr7:6889162-6889212	SAEC	small airway:	n/a
23	chr7:6887294-6887344	HCM	heart:	n/a
24	chr7:6921561-6921611	HL-60	blood:	n/a
25	chr7:6979239-6979289	HEK293	kidney:	embryo
26	chr7:6914498-6914548	NHDF-neo	bronchial:	n/a
27	chr7:6893553-6893603	HAEpiC	amniotic membrane:	n/a
28	chr7:6897353-6897403	A549	lung:	n/a
29	chr7:6897353-6897403	ECC-1	luminal epithelium:	n/a
30	chr7:6974758-6974808	RPTEC	kidney:	n/a
31	chr7:6889129-6889179	HL-60	blood:	n/a
32	chr7:6886021-6886071	HIPEpiC	eye:	n/a
33	chr7:6979488-6979538	BE2_C	brain:	n/a
34	chr7:6882194-6882244	HCF	heart:	n/a
35	chr7:6884098-6884148	SK-N-MC	brain:	n/a
36	chr7:6911211-6911261	PFSK-1	brain:	n/a
37	chr7:6979488-6979538	HUVEC	blood vessel:	n/a
38	chr7:6915894-6915944	HCM	heart:	n/a
39	chr7:6892980-6893030	Hela-S3	cervix:	n/a
40	chr7:6882112-6882162	Caco-2	colon:	n/a
41	chr7:6914289-6914339	T-47D	breast:	n/a
42	chr7:6915508-6915558	NH-A	brain:	n/a
43	chr7:6979239-6979289	MCF-7	breast:	n/a
44	chr7:6865965-6866015	HCT-116	colon:	n/a
45	chr7:6882112-6882162	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:6974892-6974942	HUVEC	blood vessel:	n/a
47	chr7:6887532-6887582	ProgFib	skin:	n/a
48	chr7:6974892-6974942	HAEpiC	amniotic membrane:	n/a
49	chr7:6893572-6893622	HepG2	liver:	n/a
50	chr7:6895389-6895439	NB4	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6144018..6145898-chr7:6967333..6970236,2	K562	blood:
2	chr7:6487483..6489084-chr7:6871444..6873922,2	MCF-7	breast:
3	chr7:6628333..6631201-chr7:6866874..6868650,2	MCF-7	breast:
4	chr7:6865395..6868378-chr7:6875321..6876917,2	MCF-7	breast:
5	chr7:6629513..6630064-chr7:6897112..6897752,3	MCF-7	breast:
6	chr7:6362339..6362861-chr7:6969838..6970665,2	K562	blood:
7	chr7:6865923..6867484-chr7:6871034..6873441,2	MCF-7	breast:
8	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:
9	chr7:6865395..6868378-chr7:6875321..6876917,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCZ1B-5	chr7:6963709-6964144	NONHSAT119086

No data

Variant related genes	Relation type
ALG1L5P	TF binding region
FAM86LP	TF binding region
ENSG00000241539	TF binding region
OR7E136P	TF binding region
CCZ1B	TF binding region
ENSG00000263457	TF binding region
ENSG00000243531	TF binding region
UNC93B2	TF binding region
OR7E59P	TF binding region
OR7E39P	TF binding region
ALG1L5P	CpG island
FAM86LP	CpG island
ENSG00000241539	CpG island
OR7E136P	CpG island
CCZ1B	CpG island
ENSG00000263457	CpG island
ENSG00000243531	CpG island
UNC93B2	CpG island
OR7E59P	CpG island
OR7E39P	CpG island
ENSG00000232581	chromatin interactions
ENSG00000146574	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000273252	chromatin interactions
ENSG00000146576	chromatin interactions

Extended variants
information (count: 7208 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7208 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3779099	chr7:6855510-6855511	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs562966201	chr7:6855541-6855542	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs531061738	chr7:6855578-6855579	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549273551	chr7:6855619-6855620	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373674006	chr7:6855627-6855628	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs74688574	chr7:6855646-6855647	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546753115	chr7:6855729-6855730	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs141370623	chr7:6855730-6855731	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs538780688	chr7:6855789-6855790	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs557349046	chr7:6855792-6855793	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs569284787	chr7:6855832-6855833	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs537336213	chr7:6855842-6855843	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs555746698	chr7:6855865-6855866	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs371840121	chr7:6855868-6855869	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs573734346	chr7:6855873-6855874	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185671538	chr7:6855889-6855890	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs376012963	chr7:6855905-6855906	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs552908869	chr7:6855929-6855930	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs375094857	chr7:6855932-6855933	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs576687156	chr7:6855940-6855941	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs368470392	chr7:6856012-6856013	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs187911937	chr7:6856031-6856032	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs150244015	chr7:6856044-6856045	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs62441816	chr7:6856049-6856050	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs574125588	chr7:6856072-6856073	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs530463386	chr7:6856078-6856079	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs542909170	chr7:6856089-6856090	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs541424395	chr7:6856090-6856091	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs2711251	chr7:6856099-6856100	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs77142976	chr7:6856115-6856116	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs558239516	chr7:6856116-6856117	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs62441817	chr7:6856137-6856138	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs547135607	chr7:6856141-6856142	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs368996172	chr7:6856153-6856154	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs533240387	chr7:6856159-6856160	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs62441818	chr7:6856174-6856175	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569274735	chr7:6856180-6856181	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs536673976	chr7:6856186-6856187	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs549283126	chr7:6856210-6856211	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567518240	chr7:6856264-6856265	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs534633267	chr7:6856265-6856266	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs553083969	chr7:6856274-6856275	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577770916	chr7:6856318-6856319	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs143914929	chr7:6856323-6856324	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191121293	chr7:6856339-6856340	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs79869764	chr7:6856340-6856341	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs374916116	chr7:6856375-6856376	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs71524079	chr7:6856387-6856388	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574868525	chr7:6856439-6856440	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548911646	chr7:6856476-6856477	Weak transcription Strong transcription	TF binding region	1 gene(s)	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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6831400-6856600	Weak transcription	Thymus	Thymus
2	chr7:6832000-6856000	Weak transcription	Fetal Brain Female	brain
3	chr7:6832000-6856400	Weak transcription	Fetal Intestine Large	intestine
4	chr7:6832000-6864600	Weak transcription	Primary T cells from cord blood	blood
5	chr7:6832000-6864800	Weak transcription	Fetal Thymus	thymus
6	chr7:6832200-6860800	Weak transcription	Brain Anterior Caudate	brain
7	chr7:6832400-6856600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:6832400-6864600	Weak transcription	Fetal Lung	lung
9	chr7:6832600-6858000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr7:6832600-6861000	Weak transcription	HUVEC	blood vessel
11	chr7:6832600-6864600	Weak transcription	NHLF	lung
12	chr7:6833000-6865200	Weak transcription	Left Ventricle	heart
13	chr7:6833000-6865200	Weak transcription	Ovary	ovary
14	chr7:6833200-6865200	Weak transcription	Pancreas	Pancrea
15	chr7:6833600-6864600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr7:6833600-6865200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr7:6834000-6866000	Weak transcription	Gastric	stomach
18	chr7:6840000-6865200	Weak transcription	Colonic Mucosa	Colon
19	chr7:6846600-6864600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr7:6847400-6864600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr7:6847600-6857200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr7:6847800-6864800	Weak transcription	NH-A	brain
23	chr7:6848200-6860600	Weak transcription	Aorta	Aorta
24	chr7:6848200-6864600	Weak transcription	Colon Smooth Muscle	Colon
25	chr7:6848400-6864800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:6848800-6863400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:6849000-6856600	Weak transcription	Brain Hippocampus Middle	brain
28	chr7:6849000-6858200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:6849000-6863200	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr7:6849000-6863200	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr7:6849000-6864600	Weak transcription	Brain Angular Gyrus	brain
32	chr7:6849200-6856600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr7:6849400-6856600	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr7:6849400-6858600	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr7:6849400-6862800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr7:6849400-6863000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:6849600-6863400	Strong transcription	Fetal Stomach	stomach
38	chr7:6849800-6864600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr7:6850000-6861800	Strong transcription	Adipose Nuclei	Adipose
40	chr7:6850000-6863200	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr7:6850200-6855800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr7:6850400-6860400	Weak transcription	Brain Substantia Nigra	brain
43	chr7:6850400-6865200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:6850400-6866000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr7:6850600-6855600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:6850600-6863400	Strong transcription	Fetal Intestine Small	intestine
47	chr7:6851200-6858000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:6851400-6861000	Weak transcription	NHEK	skin
49	chr7:6851400-6864600	Weak transcription	GM12878-XiMat	blood
50	chr7:6851400-6864800	Weak transcription	K562	blood

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