Variant report

Variant	nsv888547
Chromosome Location	chr7:80296054-80311794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:80307674-80308492	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80310661-80310891	HepG2	liver:	n/a	n/a
3	BRCA1	chr7:80302176-80302364	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr7:80304753-80304818	HepG2	liver:	n/a	chr7:80304766-80304779 chr7:80304766-80304777
5	CREB1	chr7:80309928-80310263	GM12878	blood:	n/a	n/a
6	CTCF	chr7:80310770-80310811	MCF-7	breast:	n/a	chr7:80310777-80310786
7	CTCF	chr7:80310694-80310906	HepG2	liver:	n/a	chr7:80310777-80310786
8	CTCF	chr7:80310785-80310832	GM12892	blood:	n/a	n/a
9	CTCF	chr7:80310720-80310870	AG09309	skin:	n/a	chr7:80310777-80310786
10	CTCF	chr7:80310740-80310890	HFF-Myc	foreskin:	n/a	chr7:80310777-80310786
11	CTCF	chr7:80310680-80310830	NHLF	lung:	n/a	chr7:80310777-80310786
12	CTCF	chr7:80310720-80310870	GM12872	blood:	n/a	chr7:80310777-80310786
13	CTCF	chr7:80310700-80310850	GM06990	blood:	n/a	chr7:80310777-80310786
14	CTCF	chr7:80310660-80310810	Caco-2	colon:	n/a	chr7:80310777-80310786
15	CTCF	chr7:80310700-80310850	HMEC	breast:	n/a	chr7:80310777-80310786
16	CTCF	chr7:80310820-80310970	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr7:80310733-80310882	Fibrobl	skin:	n/a	chr7:80310777-80310786
18	CTCF	chr7:80310483-80311085	HCT-116	colon:	n/a	chr7:80310777-80310786
19	CTCF	chr7:80310780-80310930	GM12866	blood:	n/a	n/a
20	CTCF	chr7:80308252-80308341	HepG2	liver:	n/a	n/a
21	CTCF	chr7:80308260-80308410	HepG2	liver:	n/a	n/a
22	CTCF	chr7:80308300-80308450	GM06990	blood:	n/a	n/a
23	CTCF	chr7:80310700-80310850	GM12873	blood:	n/a	chr7:80310777-80310786
24	CTCF	chr7:80310700-80310850	AG09319	gingival:	n/a	chr7:80310777-80310786
25	CTCF	chr7:80310760-80310910	A549	lung:	n/a	chr7:80310777-80310786
26	CTCF	chr7:80310680-80310830	GM12875	blood:	n/a	chr7:80310777-80310786
27	CTCF	chr7:80311000-80311150	GM12870	blood:	n/a	n/a
28	CTCF	chr7:80310720-80310870	GM06990	blood:	n/a	chr7:80310777-80310786
29	CTCF	chr7:80310680-80310830	HVMF	connective:	n/a	chr7:80310777-80310786
30	CTCF	chr7:80310700-80310850	GM12801	blood:	n/a	chr7:80310777-80310786
31	CTCF	chr7:80310673-80310866	GM13977	blood:	n/a	chr7:80310777-80310786
32	CTCF	chr7:80308220-80308370	Caco-2	colon:	n/a	n/a
33	CTCF	chr7:80310740-80310890	GM12871	blood:	n/a	chr7:80310777-80310786
34	CTCF	chr7:80310700-80310850	HCFaa	heart:	n/a	chr7:80310777-80310786
35	CTCF	chr7:80310680-80310830	HMF	breast:	n/a	chr7:80310777-80310786
36	CTCF	chr7:80310740-80310890	GM12867	blood:	n/a	chr7:80310777-80310786
37	CTCF	chr7:80311260-80311410	HMF	breast:	n/a	n/a
38	CTCF	chr7:80310700-80310850	AG10803	skin:	n/a	chr7:80310777-80310786
39	CTCF	chr7:80310700-80310850	AG04449	skin:	n/a	chr7:80310777-80310786
40	CTCF	chr7:80310600-80310750	HVMF	connective:	n/a	n/a
41	CTCF	chr7:80310699-80310879	Lung_OC	lung:	n/a	chr7:80310777-80310786
42	CTCF	chr7:80310680-80310830	NHEK	skin:	n/a	chr7:80310777-80310786
43	CTCF	chr7:80310680-80310830	WERI-Rb-1	eye:	n/a	chr7:80310777-80310786
44	CTCF	chr7:80310680-80310830	GM12872	blood:	n/a	chr7:80310777-80310786
45	CTCF	chr7:80310700-80310850	HepG2	liver:	n/a	chr7:80310777-80310786
46	CTCF	chr7:80310700-80310850	AoAF	blood vessel:	n/a	chr7:80310777-80310786
47	CTCF	chr7:80310680-80310830	AG10803	skin:	n/a	chr7:80310777-80310786
48	CTCF	chr7:80310672-80310888	GM12878	blood:	n/a	chr7:80310777-80310786
49	CTCF	chr7:80310726-80310846	GM10248	blood:	n/a	chr7:80310777-80310786
50	CTCF	chr7:80310723-80310881	A549	lung:	n/a	chr7:80310777-80310786

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80305251-80305301	GM12891	blood:	n/a
2	chr7:80305251-80305301	SK-N-SH_RA	brain:	n/a
3	chr7:80305251-80305301	HepG2	liver:	n/a
4	chr7:80305251-80305301	HCT-116	colon:	n/a
5	chr7:80305251-80305301	ECC-1	luminal epithelium:	n/a
6	chr7:80305251-80305301	GM12878	blood:	n/a
7	chr7:80305251-80305301	HEK293	kidney:	embryo
8	chr7:80305251-80305301	HL-60	blood:	n/a
9	chr7:80305251-80305301	HCPEpiC	choroid plexus:	n/a
10	chr7:80305251-80305301	HRE	kidney:	n/a
11	chr7:80305251-80305301	PrEC	prostate:	n/a
12	chr7:80305251-80305301	MCF-7	breast:	n/a
13	chr7:80305251-80305301	LNCaP	prostate:	n/a
14	chr7:80305251-80305301	PANC-1	pancreas:	n/a
15	chr7:80305251-80305301	HCF	heart:	n/a
16	chr7:80305251-80305301	ovcar-3	ovarian:	n/a
17	chr7:80305251-80305301	H1-hESC	embryonic stem cell:	embryo
18	chr7:80305251-80305301	GM19239	blood:	n/a
19	chr7:80305251-80305301	K562	blood:	n/a
20	chr7:80305251-80305301	AG09319	gingival:	n/a
21	chr7:80305251-80305301	HNPCEpiC	eye:	n/a
22	chr7:80305251-80305301	Jurkat	blood:	n/a
23	chr7:80305251-80305301	HIPEpiC	eye:	n/a
24	chr7:80305251-80305301	NH-A	brain:	n/a
25	chr7:80305251-80305301	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:80305251-80305301	A549	lung:	n/a
27	chr7:80305251-80305301	CMK	blood:	n/a
28	chr7:80305251-80305301	NHDF-neo	bronchial:	n/a
29	chr7:80305251-80305301	MCF10A-Er-Src	breast:	n/a
30	chr7:80305251-80305301	AG10803	skin:	n/a
31	chr7:80305251-80305301	AoSMC	blood vessel:	n/a
32	chr7:80305251-80305301	HAEpiC	amniotic membrane:	n/a
33	chr7:80305251-80305301	SKMC	muscle:	n/a
34	chr7:80305251-80305301	AG09309	skin:	n/a
35	chr7:80305251-80305301	HEEpiC	esophagus:	n/a
36	chr7:80305251-80305301	SAEC	small airway:	n/a
37	chr7:80305251-80305301	SK-N-SH	brain:	n/a
38	chr7:80305251-80305301	HRCEpiC	kidney:	n/a
39	chr7:80305251-80305301	HCM	heart:	n/a
40	chr7:80305251-80305301	Hepatocyte	liver:	n/a
41	chr7:80305251-80305301	ProgFib	skin:	n/a
42	chr7:80305251-80305301	Hela-S3	cervix:	n/a
43	chr7:80305251-80305301	BE2_C	brain:	n/a
44	chr7:80305251-80305301	U87	brain:	n/a
45	chr7:80305251-80305301	IMR90	lung:	fetal
46	chr7:80305251-80305301	GM06990	blood:	n/a
47	chr7:80305251-80305301	AG04450	lung:	fetal
48	chr7:80305251-80305301	SK-N-MC	brain:	n/a
49	chr7:80305251-80305301	RPTEC	kidney:	n/a
50	chr7:80305251-80305301	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:80296853..80299195-chr7:80307235..80310003,2	MCF-7	breast:
2	chr7:80296853..80299195-chr7:80307235..80310003,2	MCF-7	breast:
3	chr7:80057501..80059024-chr7:80309987..80311233,7	MCF-7	breast:
4	chr7:80290704..80291673-chr7:80310324..80310826,2	MCF-7	breast:
5	chr7:80309635..80311970-chr7:80327304..80328967,2	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location
1	CD36	hsa-miR-155-5p	chr7:80308392-80308413
2	CD36	hsa-miR-155-5p	chr7:80306164-80306186
3	CD36	hsa-miR-26b-5p	chr7:80303497-80303519
4	CD36	hsa-miR-155-5p	chr7:80306787-80306809

Variant related genes	Relation type
ENSG00000229436	TF binding region
CD36	TF binding region
ENSG00000229436	CpG island
CD36	CpG island

Extended variants
information (count: 773 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3212013	chr7:80296054-80296055	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs3211920	chr7:80296068-80296069	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs541359523	chr7:80296087-80296088	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs375408200	chr7:80296093-80296094	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs189518622	chr7:80296105-80296106	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs548761168	chr7:80296153-80296154	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs530960157	chr7:80296175-80296176	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs192167463	chr7:80296182-80296183	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567278746	chr7:80296197-80296198	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs529883559	chr7:80296263-80296264	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs570996005	chr7:80296264-80296265	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs184244402	chr7:80296313-80296314	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs368765791	chr7:80296343-80296344	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs538553775	chr7:80296344-80296345	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs189353208	chr7:80296366-80296367	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs3211921	chr7:80296429-80296430	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs11574716	chr7:80296458-80296459	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs553830937	chr7:80296459-80296460	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs185534292	chr7:80296482-80296483	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536847552	chr7:80296522-80296523	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs3211922	chr7:80296534-80296535	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs3211923	chr7:80296535-80296536	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545732186	chr7:80296541-80296542	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs189557598	chr7:80296553-80296554	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs180803568	chr7:80296558-80296559	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs1527484	chr7:80296562-80296563	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs11574718	chr7:80296598-80296599	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs557559015	chr7:80296599-80296600	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs186618963	chr7:80296630-80296631	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs190128201	chr7:80296631-80296632	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs62461725	chr7:80296657-80296658	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs143603914	chr7:80296659-80296660	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs552029025	chr7:80296671-80296672	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs564416939	chr7:80296745-80296746	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs17265158	chr7:80296792-80296793	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181606255	chr7:80296793-80296794	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs147067420	chr7:80296807-80296808	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs560687872	chr7:80296815-80296816	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs138362290	chr7:80296840-80296841	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536357553	chr7:80296854-80296855	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556684829	chr7:80296892-80296893	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs59984852	chr7:80296910-80296911	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17154258	chr7:80296930-80296931	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs28462358	chr7:80296958-80296959	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375552485	chr7:80296964-80296965	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144658219	chr7:80296965-80296966	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs57149211	chr7:80296974-80296975	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200294763	chr7:80296975-80296976	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372098935	chr7:80297018-80297019	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374182035	chr7:80297023-80297024	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Breast cancer	21611746	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80269400-80305000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:80279000-80306600	Weak transcription	Fetal Intestine Small	intestine
3	chr7:80279800-80303400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:80284600-80309800	Weak transcription	Psoas Muscle	Psoas
5	chr7:80285800-80308200	Weak transcription	Liver	Liver
6	chr7:80288600-80306800	Weak transcription	Lung	lung
7	chr7:80288800-80301800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr7:80288800-80308200	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr7:80288800-80309600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:80289000-80305000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:80289000-80308400	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr7:80290200-80299200	Strong transcription	Skeletal Muscle Female	skeletal muscle
13	chr7:80291800-80299600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:80291800-80305400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr7:80292000-80305200	Weak transcription	Right Ventricle	heart
16	chr7:80292000-80307400	Weak transcription	Spleen	Spleen
17	chr7:80292200-80296400	Weak transcription	Left Ventricle	heart
18	chr7:80292200-80303600	Weak transcription	Fetal Muscle Leg	muscle
19	chr7:80293600-80304400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:80294200-80305800	Strong transcription	Adipose Nuclei	Adipose
21	chr7:80294400-80299400	Weak transcription	Fetal Intestine Large	intestine
22	chr7:80294800-80296400	Strong transcription	Placenta	Placenta
23	chr7:80295200-80296400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:80295400-80300400	Strong transcription	Skeletal Muscle Male	skeletal muscle
25	chr7:80296000-80309000	Weak transcription	Fetal Heart	heart
26	chr7:80296400-80297400	Genic enhancers	Left Ventricle	heart
27	chr7:80296400-80302400	Weak transcription	Placenta	Placenta
28	chr7:80296400-80315800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:80297400-80298800	Weak transcription	Left Ventricle	heart
30	chr7:80298800-80299000	Genic enhancers	Left Ventricle	heart
31	chr7:80299000-80299800	Enhancers	Placenta Amnion	Placenta Amnion
32	chr7:80299000-80300600	Strong transcription	Left Ventricle	heart
33	chr7:80299200-80302200	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr7:80299600-80299800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:80300400-80302600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr7:80300600-80305000	Weak transcription	Left Ventricle	heart
37	chr7:80300800-80301000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:80302200-80306000	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr7:80302400-80302800	Strong transcription	Placenta	Placenta
40	chr7:80302600-80305600	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr7:80302800-80303800	Weak transcription	Placenta	Placenta
42	chr7:80303000-80303400	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr7:80303400-80304200	Strong transcription	Duodenum Mucosa	Duodenum
44	chr7:80303400-80311200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr7:80303800-80304600	Strong transcription	Placenta	Placenta
46	chr7:80304200-80307400	Weak transcription	Duodenum Mucosa	Duodenum
47	chr7:80304200-80307600	Enhancers	NHEK	skin
48	chr7:80304400-80304800	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:80304400-80307600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:80304600-80304800	Weak transcription	Placenta	Placenta

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