Variant report

Variant	nsv888534
Chromosome Location	chr7:80275455-80279460
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	FOS	chr7:80275441-80275461	MCF10A-Er-Src	breast:	n/a	n/a
2	GATA1	chr7:80274953-80276274	PBDE	blood:	n/a	chr7:80275691-80275698 chr7:80275691-80275698 chr7:80275530-80275539 chr7:80275691-80275698 chr7:80275523-80275544 chr7:80275686-80275702
3	GATA1	chr7:80275395-80275883	PBDEFetal	blood:	n/a	chr7:80275691-80275698 chr7:80275691-80275698 chr7:80275530-80275539 chr7:80275691-80275698 chr7:80275523-80275544 chr7:80275686-80275702
4	GATA3	chr7:80278227-80278232	SH-SY5Y	brain:	n/a	n/a
5	MAFF	chr7:80277533-80277897	HepG2	liver:	n/a	chr7:80277702-80277720
6	MAFF	chr7:80277544-80277887	K562	blood:	n/a	chr7:80277702-80277720
7	MAFK	chr7:80277540-80277870	H1-hESC	embryonic stem cell:	n/a	chr7:80277704-80277715 chr7:80277704-80277720 chr7:80277704-80277715 chr7:80277704-80277719
8	MAFK	chr7:80277534-80277897	IMR90	lung:	n/a	chr7:80277704-80277715 chr7:80277704-80277720 chr7:80277704-80277715 chr7:80277704-80277719
9	MAFK	chr7:80277571-80277863	Hela-S3	cervix:	n/a	chr7:80277704-80277715 chr7:80277704-80277720 chr7:80277704-80277715 chr7:80277704-80277719
10	MAFK	chr7:80277542-80277879	HepG2	liver:	n/a	chr7:80277704-80277715 chr7:80277704-80277720 chr7:80277704-80277715 chr7:80277704-80277719
11	MAFK	chr7:80277529-80277896	HepG2	liver:	n/a	chr7:80277704-80277715 chr7:80277704-80277720 chr7:80277704-80277715 chr7:80277704-80277719
12	MAFK	chr7:80277543-80277879	K562	blood:	n/a	chr7:80277704-80277715 chr7:80277704-80277720 chr7:80277704-80277715 chr7:80277704-80277719
13	NFYB	chr7:80278483-80278598	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr7:80275071-80287547	PBDE	blood:	n/a	n/a
15	POLR2A	chr7:80277125-80277242	MCF10A-Er-Src	breast:	n/a	n/a
16	STAT3	chr7:80277054-80277193	MCF10A-Er-Src	breast:	n/a	n/a
17	TAL1	chr7:80275583-80275600	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80275870-80275920	HEK293	kidney:	embryo
2	chr7:80275870-80275920	PANC-1	pancreas:	n/a
3	chr7:80275870-80275920	HNPCEpiC	eye:	n/a
4	chr7:80275870-80275920	GM12878	blood:	n/a
5	chr7:80275870-80275920	NB4	blood:	n/a
6	chr7:80275870-80275920	HCF	heart:	n/a
7	chr7:80275870-80275920	BJ	skin:	n/a
8	chr7:80275870-80275920	IMR90	lung:	fetal
9	chr7:80275870-80275920	GM12892	blood:	n/a
10	chr7:80275870-80275920	SK-N-MC	brain:	n/a
11	chr7:80275870-80275920	AoSMC	blood vessel:	n/a
12	chr7:80275870-80275920	RPTEC	kidney:	n/a
13	chr7:80275870-80275920	NH-A	brain:	n/a
14	chr7:80275870-80275920	NHBE	bronchial:	n/a
15	chr7:80275870-80275920	A549	lung:	n/a
16	chr7:80275870-80275920	HCM	heart:	n/a
17	chr7:80275870-80275920	AG04449	skin:	fetal
18	chr7:80275870-80275920	HRE	kidney:	n/a
19	chr7:80275870-80275920	PrEC	prostate:	n/a
20	chr7:80275870-80275920	HCPEpiC	choroid plexus:	n/a
21	chr7:80275870-80275920	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:80275870-80275920	ovcar-3	ovarian:	n/a
23	chr7:80275870-80275920	GM12891	blood:	n/a
24	chr7:80275870-80275920	U87	brain:	n/a
25	chr7:80275870-80275920	MCF10A-Er-Src	breast:	n/a
26	chr7:80275870-80275920	Caco-2	colon:	n/a
27	chr7:80275870-80275920	HepG2	liver:	n/a
28	chr7:80275870-80275920	HMEC	breast:	n/a
29	chr7:80275870-80275920	ECC-1	luminal epithelium:	n/a
30	chr7:80275870-80275920	K562	blood:	n/a
31	chr7:80275870-80275920	AG09309	skin:	n/a
32	chr7:80275870-80275920	SAEC	small airway:	n/a
33	chr7:80275870-80275920	HIPEpiC	eye:	n/a
34	chr7:80275870-80275920	GM19239	blood:	n/a
35	chr7:80275870-80275920	BE2_C	brain:	n/a
36	chr7:80275870-80275920	T-47D	breast:	n/a
37	chr7:80275870-80275920	HCT-116	colon:	n/a
38	chr7:80275870-80275920	HL-60	blood:	n/a
39	chr7:80275870-80275920	NHDF-neo	bronchial:	n/a
40	chr7:80275870-80275920	AG09319	gingival:	n/a
41	chr7:80275870-80275920	HRPEpiC	eye:	n/a
42	chr7:80275870-80275920	PFSK-1	brain:	n/a
43	chr7:80275870-80275920	NT2-D1	testis:	n/a
44	chr7:80275870-80275920	AG04450	lung:	fetal
45	chr7:80275870-80275920	ProgFib	skin:	n/a
46	chr7:80275870-80275920	Hela-S3	cervix:	n/a
47	chr7:80275870-80275920	Hepatocyte	liver:	n/a
48	chr7:80275870-80275920	HEEpiC	esophagus:	n/a
49	chr7:80275870-80275920	HUVEC	blood vessel:	n/a
50	chr7:80275870-80275920	GM06990	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121746
2	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121745
3	lnc-GNAI1-5	chr7:80275968-80276531	NONHSAT121745
4	lnc-GNAI1-5	chr7:80275968-80276042	NONHSAT121746

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

Extended variants
information (count: 170 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:170 , 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	rs1049654	chr7:80275455-80275456	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566379897	chr7:80275463-80275464	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs529130978	chr7:80275491-80275492	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs567633234	chr7:80275503-80275504	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs13306228	chr7:80275519-80275520	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs568330281	chr7:80275552-80275553	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs537473704	chr7:80275555-80275556	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs3211805	chr7:80275576-80275577	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs575034427	chr7:80275584-80275585	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs139292358	chr7:80275617-80275618	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs539977067	chr7:80275661-80275662	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs372978118	chr7:80275681-80275682	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs561862760	chr7:80275737-80275738	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs55849243	chr7:80275741-80275742	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs143736571	chr7:80275761-80275762	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573387511	chr7:80275823-80275824	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146810370	chr7:80275870-80275871	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs534111289	chr7:80275885-80275886	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs538254881	chr7:80275895-80275896	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs543791697	chr7:80275940-80275941	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs563780469	chr7:80275949-80275950	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs532861034	chr7:80275991-80275992	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs369908271	chr7:80276006-80276007	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs371762333	chr7:80276012-80276013	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs542707504	chr7:80276020-80276021	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs75112981	chr7:80276038-80276039	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs13306226	chr7:80276039-80276040	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs201759988	chr7:80276061-80276062	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs13306227	chr7:80276070-80276071	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs559876270	chr7:80276079-80276080	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs375008822	chr7:80276086-80276087	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs368907671	chr7:80276087-80276088	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs143724791	chr7:80276111-80276112	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs555637878	chr7:80276181-80276182	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs575810467	chr7:80276189-80276190	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs373416118	chr7:80276197-80276198	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs140457847	chr7:80276200-80276201	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs371515972	chr7:80276223-80276224	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs3211806	chr7:80276227-80276228	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs9282633	chr7:80276286-80276287	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs548976088	chr7:80276323-80276324	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs572241103	chr7:80276324-80276325	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs1527463	chr7:80276331-80276332	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs9282634	chr7:80276356-80276357	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs9282635	chr7:80276414-80276415	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs569569046	chr7:80276416-80276417	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs531539911	chr7:80276417-80276418	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs538278752	chr7:80276418-80276419	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs550982554	chr7:80276426-80276427	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs570904196	chr7:80276429-80276430	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80269400-80305000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:80272000-80280400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:80272600-80293600	Weak transcription	Placenta	Placenta
4	chr7:80272800-80282600	Weak transcription	Fetal Heart	heart
5	chr7:80273000-80275600	Weak transcription	HepG2	liver
6	chr7:80273200-80275800	Weak transcription	Psoas Muscle	Psoas
7	chr7:80273600-80275600	Weak transcription	Right Ventricle	heart
8	chr7:80273600-80278400	Weak transcription	Small Intestine	intestine
9	chr7:80273800-80278200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr7:80274000-80276200	Genic enhancers	Monocytes-CD14+_RO01746	blood
11	chr7:80275200-80276000	Enhancers	NHDF-Ad	bronchial
12	chr7:80275200-80277600	Transcr. at gene 5' and 3'	Adipose Nuclei	Adipose
13	chr7:80275200-80277600	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr7:80275200-80277600	Active TSS	Right Atrium	heart
15	chr7:80275400-80275600	Enhancers	Duodenum Mucosa	Duodenum
16	chr7:80275400-80275600	Enhancers	Fetal Intestine Small	intestine
17	chr7:80275400-80275800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:80275400-80275800	Enhancers	Liver	Liver
19	chr7:80275400-80275800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
20	chr7:80275400-80276000	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:80275400-80276200	Genic enhancers	Primary monocytes fromperipheralblood	blood
22	chr7:80275400-80276200	Transcr. at gene 5' and 3'	Left Ventricle	heart
23	chr7:80275600-80275800	Flanking Active TSS	Right Ventricle	heart
24	chr7:80275600-80276200	Enhancers	HepG2	liver
25	chr7:80275600-80276600	Active TSS	Fetal Intestine Large	intestine
26	chr7:80275600-80277600	Active TSS	Fetal Intestine Small	intestine
27	chr7:80275600-80278400	Active TSS	Duodenum Mucosa	Duodenum
28	chr7:80275800-80276000	Flanking Active TSS	Liver	Liver
29	chr7:80275800-80276000	Enhancers	Right Ventricle	heart
30	chr7:80275800-80276200	Active TSS	Psoas Muscle	Psoas
31	chr7:80275800-80284200	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr7:80275800-80288400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:80276000-80276200	Active TSS	Liver	Liver
34	chr7:80276000-80276200	Flanking Active TSS	Right Ventricle	heart
35	chr7:80276000-80280800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:80276200-80276400	Enhancers	Right Ventricle	heart
37	chr7:80276200-80277000	Weak transcription	Left Ventricle	heart
38	chr7:80276200-80284200	Weak transcription	Psoas Muscle	Psoas
39	chr7:80276200-80285600	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr7:80276200-80286400	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr7:80276400-80276800	Weak transcription	Right Ventricle	heart
42	chr7:80276600-80277000	Enhancers	Fetal Intestine Large	intestine
43	chr7:80276800-80277000	Enhancers	Right Ventricle	heart
44	chr7:80277000-80277200	Flanking Active TSS	Fetal Intestine Large	intestine
45	chr7:80277000-80277200	Genic enhancers	Left Ventricle	heart
46	chr7:80277000-80284200	Weak transcription	Right Ventricle	heart
47	chr7:80277200-80284200	Weak transcription	Left Ventricle	heart
48	chr7:80277600-80278400	Weak transcription	Fetal Intestine Small	intestine
49	chr7:80277600-80278400	Weak transcription	Right Atrium	heart
50	chr7:80277600-80282400	Genic enhancers	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links