Variant report

Variant	nsv525104
Chromosome Location	chr7:79991029-80002223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:79991513-79991691	HepG2	liver:	n/a	n/a
2	BHLHE40	chr7:80001849-80001951	GM12878	blood:	n/a	n/a
3	CTCF	chr7:80001540-80001690	HPAF	blood vessel:	n/a	n/a
4	EP300	chr7:80001580-80002289	A549	lung:	n/a	n/a
5	EP300	chr7:80001636-80002274	A549	lung:	n/a	n/a
6	EP300	chr7:80001563-80002336	SK-N-SH	brain:	n/a	n/a
7	FOS	chr7:79992078-79992336	MCF10A-Er-Src	breast:	n/a	chr7:79992206-79992217 chr7:79992208-79992216 chr7:79992208-79992215 chr7:79992208-79992216
8	FOS	chr7:79992035-79992324	HUVEC	blood vessel:	n/a	chr7:79992206-79992217 chr7:79992208-79992216 chr7:79992208-79992215 chr7:79992208-79992216
9	FOS	chr7:79992062-79992376	MCF10A-Er-Src	breast:	n/a	chr7:79992206-79992217 chr7:79992208-79992216 chr7:79992208-79992215 chr7:79992208-79992216
10	FOS	chr7:79992091-79992367	MCF10A-Er-Src	breast:	n/a	chr7:79992206-79992217 chr7:79992208-79992216 chr7:79992208-79992215 chr7:79992208-79992216
11	FOSL2	chr7:80001744-80002214	A549	lung:	n/a	n/a
12	FOSL2	chr7:79991357-79991932	A549	lung:	n/a	n/a
13	FOSL2	chr7:79991978-79992455	SK-N-SH	brain:	n/a	chr7:79992208-79992216 chr7:79992208-79992215 chr7:79992208-79992216 chr7:79992389-79992398
14	FOXA1	chr7:79991245-79991835	T-47D	breast:	n/a	n/a
15	FOXA1	chr7:79991304-79991549	T-47D	breast:	n/a	n/a
16	FOXA1	chr7:79991458-79991867	HepG2	liver:	n/a	n/a
17	FOXA2	chr7:79991370-79992021	A549	lung:	n/a	n/a
18	GATA3	chr7:79991058-79991995	A549	lung:	n/a	n/a
19	GATA3	chr7:79991267-79991713	MCF-7	breast:	n/a	n/a
20	GATA3	chr7:80001576-80002263	A549	lung:	n/a	n/a
21	GATA3	chr7:79991258-79991738	A549	lung:	n/a	n/a
22	GATA3	chr7:79991013-79991879	SK-N-SH	brain:	n/a	n/a
23	GATA3	chr7:79991281-79991683	T-47D	breast:	n/a	n/a
24	GATA3	chr7:80001492-80002298	SK-N-SH	brain:	n/a	n/a
25	GATA3	chr7:79991156-79991880	SK-N-SH	brain:	n/a	n/a
26	GATA3	chr7:80001621-80002218	SK-N-SH	brain:	n/a	n/a
27	GATA3	chr7:79991221-79991588	T-47D	breast:	n/a	n/a
28	MAFK	chr7:79991237-79991625	Hela-S3	cervix:	n/a	n/a
29	MYC	chr7:79999280-79999480	MCF10A-Er-Src	breast:	n/a	n/a
30	NFIC	chr7:80001541-80002289	SK-N-SH	brain:	n/a	n/a
31	NR3C1	chr7:79991275-79991635	A549	lung:	n/a	n/a
32	PBX3	chr7:80001652-80002295	SK-N-SH	brain:	n/a	n/a
33	PBX3	chr7:79991270-79991626	SK-N-SH	brain:	n/a	chr7:79991519-79991530
34	PBX3	chr7:79991134-79991713	SK-N-SH	brain:	n/a	chr7:79991519-79991530
35	POLR2A	chr7:79994798-79994893	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr7:80001718-80002116	SK-N-SH	brain:	n/a	n/a
37	POLR2A	chr7:79992707-79992739	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr7:79995277-79995451	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr7:80001710-80001909	ProgFib	skin:	n/a	n/a
40	POLR2A	chr7:79999963-80000245	H1-neurons	neurons:	n/a	n/a
41	POLR2A	chr7:79991309-79991609	SK-N-SH	brain:	n/a	n/a
42	RCOR1	chr7:79991246-79991695	Hela-S3	cervix:	n/a	n/a
43	SP1	chr7:80001696-80002224	A549	lung:	n/a	chr7:80002192-80002206
44	SP1	chr7:79991212-79991742	A549	lung:	n/a	n/a
45	SP1	chr7:80001692-80002236	A549	lung:	n/a	chr7:80002192-80002206
46	TCF12	chr7:79991110-79992064	A549	lung:	n/a	chr7:79991536-79991543
47	TCF12	chr7:80001600-80002252	SK-N-SH	brain:	n/a	n/a
48	TCF12	chr7:79991157-79991844	SK-N-SH	brain:	n/a	chr7:79991536-79991543
49	TCF12	chr7:79991049-79991808	SK-N-SH	brain:	n/a	chr7:79991536-79991543
50	TCF12	chr7:80001666-80002242	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:79998795-79998845	HCM	heart:	n/a
2	chr7:79998779-79998829	MCF10A-Er-Src	breast:	n/a
3	chr7:79998779-79998829	H1-hESC	embryonic stem cell:	embryo
4	chr7:79997911-79997961	SK-N-SH_RA	brain:	n/a
5	chr7:79997911-79997961	ProgFib	skin:	n/a
6	chr7:79998779-79998829	ovcar-3	ovarian:	n/a
7	chr7:79998779-79998829	HEEpiC	esophagus:	n/a
8	chr7:79998779-79998829	GM06990	blood:	n/a
9	chr7:79998779-79998829	Hela-S3	cervix:	n/a
10	chr7:79997911-79997961	AoSMC	blood vessel:	n/a
11	chr7:79998795-79998845	ProgFib	skin:	n/a
12	chr7:79998779-79998829	AG04449	skin:	fetal
13	chr7:79998779-79998829	GM12892	blood:	n/a
14	chr7:79998795-79998845	PANC-1	pancreas:	n/a
15	chr7:79998795-79998845	RPTEC	kidney:	n/a
16	chr7:79998779-79998829	LNCaP	prostate:	n/a
17	chr7:79998779-79998829	BJ	skin:	n/a
18	chr7:79997911-79997961	HNPCEpiC	eye:	n/a
19	chr7:79998779-79998829	NHBE	bronchial:	n/a
20	chr7:79998795-79998845	PFSK-1	brain:	n/a
21	chr7:79998779-79998829	A549	lung:	n/a
22	chr7:79998779-79998829	HL-60	blood:	n/a
23	chr7:79997911-79997961	HAEpiC	amniotic membrane:	n/a
24	chr7:79998795-79998845	HRE	kidney:	n/a
25	chr7:79998795-79998845	AG09319	gingival:	n/a
26	chr7:79998795-79998845	U87	brain:	n/a
27	chr7:79998795-79998845	BJ	skin:	n/a
28	chr7:79998779-79998829	NH-A	brain:	n/a
29	chr7:79998795-79998845	HCPEpiC	choroid plexus:	n/a
30	chr7:79998779-79998829	SK-N-SH	brain:	n/a
31	chr7:79998779-79998829	MCF-7	breast:	n/a
32	chr7:79998795-79998845	GM12878	blood:	n/a
33	chr7:79998795-79998845	GM12892	blood:	n/a
34	chr7:79998779-79998829	AG09319	gingival:	n/a
35	chr7:79998795-79998845	H1-hESC	embryonic stem cell:	embryo
36	chr7:79998795-79998845	NHDF-neo	bronchial:	n/a
37	chr7:79998795-79998845	NH-A	brain:	n/a
38	chr7:79998795-79998845	HNPCEpiC	eye:	n/a
39	chr7:79997911-79997961	ECC-1	luminal epithelium:	n/a
40	chr7:79998779-79998829	HCPEpiC	choroid plexus:	n/a
41	chr7:79997911-79997961	HRPEpiC	eye:	n/a
42	chr7:79997911-79997961	U87	brain:	n/a
43	chr7:79997911-79997961	HRCEpiC	kidney:	n/a
44	chr7:79997911-79997961	AG04449	skin:	fetal
45	chr7:79998779-79998829	AoSMC	blood vessel:	n/a
46	chr7:79997911-79997961	SKMC	muscle:	n/a
47	chr7:79997911-79997961	H1-hESC	embryonic stem cell:	embryo
48	chr7:79998795-79998845	GM12891	blood:	n/a
49	chr7:79998795-79998845	HCT-116	colon:	n/a
50	chr7:79998779-79998829	Jurkat	blood:	n/a

No data

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAT3-1	chr7:80000502-80000893	NONHSAT121740
2	lnc-GNAT3-1	chr7:80001443-80001610	ENSG00000232667.5
3	lnc-GNAT3-1	chr7:80000502-80000893	ENSG00000232667.5
4	lnc-GNAT3-1	chr7:80001443-80001610	NONHSAT121741
5	lnc-GNAT3-1	chr7:80001448-80001610	NONHSAT121743
6	lnc-GNAT3-1	chr7:80001443-80001610	NONHSAT121740
7	lnc-GNAT3-1	chr7:80001443-80001545	ENSG00000232667.5
8	lnc-GNAT3-1	chr7:80001443-80001610	ENSG00000232667
9	lnc-GNAT3-1	chr7:79991431-79991540	ENSG00000232667.5
10	lnc-GNAT3-1	chr7:80000833-80000893	ENSG00000232667
11	lnc-GNAT3-1	chr7:80000517-80000893	NONHSAT121741
12	lnc-GNAT3-1	chr7:80001443-80001610	ENSG00000232667.5
13	lnc-GNAT3-1	chr7:80001237-80001610	ENSG00000232667.5

No data

Variant related genes	Relation type
CD36	TF binding region
ENSG00000232667	TF binding region
CD36	CpG island
ENSG00000232667	CpG island

Extended variants
information (count: 288 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs304761	chr7:79991029-79991030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138720093	chr7:79991034-79991035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186073951	chr7:79991050-79991051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs304762	chr7:79991108-79991109	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs189616865	chr7:79991122-79991123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142948838	chr7:79991131-79991132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs304763	chr7:79991144-79991145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374416959	chr7:79991161-79991162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111925858	chr7:79991177-79991178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112870372	chr7:79991199-79991200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111577445	chr7:79991205-79991206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397737572	chr7:79991212-79991213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556099540	chr7:79991247-79991248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10255079	chr7:79991262-79991263	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545646548	chr7:79991284-79991285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1511683	chr7:79991291-79991292	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545325308	chr7:79991319-79991320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115739879	chr7:79991320-79991321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186058111	chr7:79991331-79991332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6467126	chr7:79991379-79991380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs530104900	chr7:79991407-79991408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190921492	chr7:79991434-79991435	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs183067566	chr7:79991457-79991458	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs75019817	chr7:79991471-79991472	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs17235042	chr7:79991474-79991475	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185302520	chr7:79991485-79991486	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs116703233	chr7:79991501-79991502	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs547581583	chr7:79991562-79991563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561085246	chr7:79991572-79991573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs71518983	chr7:79991577-79991578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11400036	chr7:79991584-79991585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs397891085	chr7:79991589-79991590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147459483	chr7:79991655-79991656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10486935	chr7:79991800-79991801	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs528364257	chr7:79991813-79991814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73384708	chr7:79991817-79991818	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569627093	chr7:79991859-79991860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538989813	chr7:79991882-79991883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558806601	chr7:79991894-79991895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73384709	chr7:79991901-79991902	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs573922407	chr7:79991909-79991910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs55683109	chr7:79991987-79991988	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554695162	chr7:79991989-79991990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549517375	chr7:79991996-79991997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201668277	chr7:79992004-79992005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs68189191	chr7:79992025-79992026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543883372	chr7:79992033-79992034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397889878	chr7:79992038-79992039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397709007	chr7:79992039-79992040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563560101	chr7:79992077-79992078	Enhancers Weak transcription	n/a	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
Cancer	20164919	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Hodgkin''s lymphoma	18641027	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79986200-79995400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:79987000-79991400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:79987200-79992000	Weak transcription	Osteobl	bone
4	chr7:79987600-79991800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:79991400-79992400	Enhancers	Hela-S3	cervix
6	chr7:79991400-79992400	Enhancers	HSMM	muscle
7	chr7:79991400-79992600	Enhancers	NHDF-Ad	bronchial
8	chr7:79991400-79992800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr7:79991400-79993000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr7:79991600-79992000	Enhancers	NHLF	lung
11	chr7:79991600-79992600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:79991600-79992800	Enhancers	A549	lung
13	chr7:79991800-79992400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:79991800-79992600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:79992000-79992600	Enhancers	Osteobl	bone
16	chr7:79998600-79999400	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr7:79998600-80000400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr7:79998800-79999000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:79998800-79999200	Enhancers	HUVEC	blood vessel
20	chr7:79998800-79999600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr7:79999000-79999800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:79999400-79999600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr7:79999600-79999800	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr7:79999800-80000200	Enhancers	Brain Germinal Matrix	brain
25	chr7:79999800-80000200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr7:79999800-80000400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:80000200-80000400	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr7:80000400-80000600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:80000400-80003000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:80000400-80008000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr7:80000600-80000800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:80000800-80001400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:80001200-80001600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:80001200-80001800	Enhancers	HSMMtube	muscle
35	chr7:80001200-80001800	Enhancers	NHLF	lung
36	chr7:80001200-80002800	Enhancers	HSMM	muscle
37	chr7:80001200-80003200	Enhancers	A549	lung
38	chr7:80001400-80002200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:80001400-80002600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr7:80001600-80001800	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr7:80001600-80001800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:80001600-80001800	Enhancers	Liver	Liver
43	chr7:80001600-80002400	Enhancers	Osteobl	bone
44	chr7:80001600-80002600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr7:80001800-80002000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:80001800-80002200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:80001800-80002200	Enhancers	Aorta	Aorta
48	chr7:80001800-80002200	Flanking Active TSS	Liver	Liver
49	chr7:80001800-80002200	Enhancers	Ovary	ovary
50	chr7:80001800-80002600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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