Variant report

Variant	nsv888531
Chromosome Location	chr7:80258564-80280117
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	chr7:80263770-80264169	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80272116-80272564	HepG2	liver:	n/a	n/a
3	ATF2	chr7:80267373-80268134	GM12878	blood:	n/a	n/a
4	ATF2	chr7:80267578-80268064	GM12878	blood:	n/a	n/a
5	BACH1	chr7:80260910-80260913	K562	blood:	n/a	n/a
6	BATF	chr7:80267605-80267988	GM12878	blood:	n/a	n/a
7	BATF	chr7:80267647-80267923	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:80267684-80267984	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:80267588-80268026	GM12878	blood:	n/a	n/a
10	BCL3	chr7:80267478-80268093	GM12878	blood:	n/a	chr7:80267573-80267582
11	BCLAF1	chr7:80267523-80268057	GM12878	blood:	n/a	chr7:80267573-80267582
12	BHLHE40	chr7:80267457-80267965	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:80263685-80264171	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:80263785-80264123	ECC-1	luminal epithelium:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
15	CEBPB	chr7:80268417-80268679	IMR90	lung:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
16	CEBPB	chr7:80272144-80272538	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
17	CEBPB	chr7:80272811-80273219	MCF-7	breast:	n/a	n/a
18	CEBPB	chr7:80263869-80264105	ECC-1	luminal epithelium:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
19	CEBPB	chr7:80268439-80268641	A549	lung:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
20	CEBPB	chr7:80262315-80262400	A549	lung:	n/a	chr7:80262334-80262345
21	CEBPB	chr7:80263820-80264077	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
22	CEBPB	chr7:80263803-80264151	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
23	CEBPB	chr7:80263773-80264293	IMR90	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
24	CEBPB	chr7:80262186-80262489	HepG2	liver:	n/a	chr7:80262334-80262345
25	CEBPB	chr7:80263757-80264252	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
26	CEBPB	chr7:80263755-80264281	Hela-S3	cervix:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
27	CEBPB	chr7:80267337-80268157	GM12878	blood:	n/a	chr7:80267547-80267560 chr7:80267352-80267363 chr7:80267356-80267367
28	CEBPB	chr7:80263632-80264325	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
29	CEBPB	chr7:80272854-80273198	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr7:80263790-80264179	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
31	CEBPB	chr7:80259785-80260226	MCF-7	breast:	n/a	chr7:80260003-80260014
32	CEBPB	chr7:80268410-80268678	K562	blood:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
33	CEBPB	chr7:80263777-80264203	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
34	CEBPB	chr7:80268377-80268683	HepG2	liver:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
35	CEBPB	chr7:80263676-80264299	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
36	CEBPB	chr7:80263870-80264032	K562	blood:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
37	CEBPB	chr7:80259836-80260218	Hela-S3	cervix:	n/a	chr7:80260003-80260014
38	CEBPB	chr7:80263864-80264074	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
39	CEBPB	chr7:80272830-80273384	MCF-7	breast:	n/a	n/a
40	CEBPB	chr7:80272158-80272462	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
41	CEBPB	chr7:80272790-80273832	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr7:80272148-80272537	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
43	CEBPB	chr7:80262200-80262511	Hela-S3	cervix:	n/a	chr7:80262334-80262345
44	CEBPB	chr7:80259876-80260239	MCF-7	breast:	n/a	chr7:80260003-80260014
45	CEBPB	chr7:80272188-80272426	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
46	CEBPB	chr7:80263826-80264127	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
47	CEBPD	chr7:80272223-80272481	HepG2	liver:	n/a	chr7:80272336-80272347
48	CHD2	chr7:80263854-80264150	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr7:80267673-80268042	GM12878	blood:	n/a	chr7:80267904-80267914 chr7:80267907-80267917
50	CREB1	chr7:80267543-80268149	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80275870-80275920	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:80274687-80274737	AG09309	skin:	n/a
3	chr7:80267619-80267669	HepG2	liver:	n/a
4	chr7:80275870-80275920	NH-A	brain:	n/a
5	chr7:80274460-80274510	HAEpiC	amniotic membrane:	n/a
6	chr7:80267943-80267993	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:80266930-80266980	LNCaP	prostate:	n/a
8	chr7:80267943-80267993	HCPEpiC	choroid plexus:	n/a
9	chr7:80267619-80267669	BE2_C	brain:	n/a
10	chr7:80267943-80267993	SK-N-MC	brain:	n/a
11	chr7:80275870-80275920	HNPCEpiC	eye:	n/a
12	chr7:80274460-80274510	LNCaP	prostate:	n/a
13	chr7:80274687-80274737	PrEC	prostate:	n/a
14	chr7:80275870-80275920	NHBE	bronchial:	n/a
15	chr7:80274460-80274510	HCPEpiC	choroid plexus:	n/a
16	chr7:80275870-80275920	A549	lung:	n/a
17	chr7:80274687-80274737	HCPEpiC	choroid plexus:	n/a
18	chr7:80274460-80274510	H1-hESC	embryonic stem cell:	embryo
19	chr7:80274460-80274510	HRPEpiC	eye:	n/a
20	chr7:80267619-80267669	HL-60	blood:	n/a
21	chr7:80275870-80275920	GM06990	blood:	n/a
22	chr7:80267619-80267669	HCM	heart:	n/a
23	chr7:80267619-80267669	AG04450	lung:	fetal
24	chr7:80266930-80266980	GM12878	blood:	n/a
25	chr7:80267943-80267993	PANC-1	pancreas:	n/a
26	chr7:80267619-80267669	ovcar-3	ovarian:	n/a
27	chr7:80267943-80267993	SKMC	muscle:	n/a
28	chr7:80267943-80267993	U87	brain:	n/a
29	chr7:80266930-80266980	MCF-7	breast:	n/a
30	chr7:80274460-80274510	RPTEC	kidney:	n/a
31	chr7:80274460-80274510	MCF-7	breast:	n/a
32	chr7:80266930-80266980	Jurkat	blood:	n/a
33	chr7:80267943-80267993	LNCaP	prostate:	n/a
34	chr7:80274687-80274737	SK-N-SH	brain:	n/a
35	chr7:80267619-80267669	NHDF-neo	bronchial:	n/a
36	chr7:80275870-80275920	T-47D	breast:	n/a
37	chr7:80274687-80274737	NHBE	bronchial:	n/a
38	chr7:80275870-80275920	SK-N-SH_RA	brain:	n/a
39	chr7:80274460-80274510	HCM	heart:	n/a
40	chr7:80275870-80275920	Hepatocyte	liver:	n/a
41	chr7:80267943-80267993	A549	lung:	n/a
42	chr7:80266930-80266980	HRPEpiC	eye:	n/a
43	chr7:80267619-80267669	HAEpiC	amniotic membrane:	n/a
44	chr7:80266930-80266980	AoSMC	blood vessel:	n/a
45	chr7:80267619-80267669	GM12892	blood:	n/a
46	chr7:80266930-80266980	BE2_C	brain:	n/a
47	chr7:80274460-80274510	BE2_C	brain:	n/a
48	chr7:80266930-80266980	HRCEpiC	kidney:	n/a
49	chr7:80266930-80266980	HAEpiC	amniotic membrane:	n/a
50	chr7:80275870-80275920	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:80254055..80256546-chr7:80258500..80261458,2	K562	blood:
2	chr7:80263049..80265695-chr7:80267263..80270319,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-5	chr7:80266148-80266319	NONHSAT121746
2	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121746
3	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121745
4	lnc-GNAI1-5	chr7:80275968-80276042	NONHSAT121746
5	lnc-GNAI1-4	chr7:80262513-80262678	NONHSAT121747
6	lnc-GNAI1-5	chr7:80275968-80276531	NONHSAT121745

Variant related genes	Relation type
CD36	TF binding region
CD36	CpG island
ENSG00000135218	chromatin interactions

Extended variants
information (count: 808 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:808 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532393487	chr7:80258593-80258594	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs190758490	chr7:80258600-80258601	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs11770907	chr7:80258630-80258631	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs114884425	chr7:80258631-80258632	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182989990	chr7:80258670-80258671	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567359660	chr7:80258679-80258680	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530127209	chr7:80258681-80258682	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs115529856	chr7:80258764-80258765	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs116030333	chr7:80258777-80258778	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373617426	chr7:80258799-80258800	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs10499859	chr7:80258810-80258811	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
12	rs143768584	chr7:80258817-80258818	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535035360	chr7:80258819-80258820	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs554589566	chr7:80258825-80258826	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs73378947	chr7:80258832-80258833	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs537138756	chr7:80258841-80258842	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs76416388	chr7:80258863-80258864	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370851742	chr7:80258891-80258892	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs73152252	chr7:80258898-80258899	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs375739648	chr7:80259047-80259048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114530954	chr7:80259052-80259053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1572230	chr7:80259082-80259083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs560945713	chr7:80259178-80259179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs77081334	chr7:80259213-80259214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150585374	chr7:80259215-80259216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs529928493	chr7:80259216-80259217	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs56195239	chr7:80259226-80259227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556236042	chr7:80259227-80259228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530041050	chr7:80259234-80259235	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs146699378	chr7:80259288-80259289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376412566	chr7:80259291-80259292	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs187956372	chr7:80259298-80259299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs193226505	chr7:80259355-80259356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs150118955	chr7:80259447-80259448	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369963145	chr7:80259450-80259451	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532570647	chr7:80259508-80259509	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552716123	chr7:80259510-80259511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs139069545	chr7:80259529-80259530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs114020567	chr7:80259629-80259630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs565743809	chr7:80259831-80259832	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370803638	chr7:80259854-80259855	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373654139	chr7:80259869-80259870	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs17263407	chr7:80259908-80259909	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs537051307	chr7:80259909-80259910	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs149878320	chr7:80259920-80259921	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs13312376	chr7:80259931-80259932	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs4316098	chr7:80259988-80259989	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539183336	chr7:80260019-80260020	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4626520	chr7:80260023-80260024	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs13311175	chr7:80260068-80260069	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	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:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80251800-80260000	Weak transcription	Right Ventricle	heart
2	chr7:80252000-80260000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:80253400-80259400	Weak transcription	Fetal Lung	lung
4	chr7:80254800-80259400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr7:80254800-80259600	Weak transcription	HepG2	liver
6	chr7:80255400-80259800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:80255400-80260000	Weak transcription	Right Atrium	heart
8	chr7:80255600-80260200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:80255800-80261800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:80256400-80261600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:80256800-80259600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:80256800-80260000	Weak transcription	NHDF-Ad	bronchial
13	chr7:80257000-80259000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:80257000-80259400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:80257000-80259600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr7:80257400-80258600	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr7:80257400-80259800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:80257800-80259000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:80257800-80260400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr7:80258000-80258600	Enhancers	Psoas Muscle	Psoas
21	chr7:80258000-80258800	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr7:80258000-80262800	Enhancers	Fetal Heart	heart
23	chr7:80258400-80258600	Flanking Active TSS	Left Ventricle	heart
24	chr7:80258400-80260000	Enhancers	Adipose Nuclei	Adipose
25	chr7:80258600-80259400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr7:80258600-80259800	Weak transcription	Psoas Muscle	Psoas
27	chr7:80258600-80264800	Weak transcription	Left Ventricle	heart
28	chr7:80258800-80259800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr7:80259000-80260200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:80259000-80260200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:80259400-80260000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:80259400-80260000	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr7:80259400-80260200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr7:80259400-80260400	Enhancers	Small Intestine	intestine
35	chr7:80259400-80261600	Enhancers	Fetal Lung	lung
36	chr7:80259600-80259800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:80259600-80260000	Enhancers	HepG2	liver
38	chr7:80259600-80262400	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr7:80259600-80263400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:80259800-80260000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:80259800-80260000	Active TSS	Psoas Muscle	Psoas
42	chr7:80259800-80260000	Enhancers	Rectal Smooth Muscle	rectum
43	chr7:80259800-80260000	Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr7:80259800-80260200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr7:80259800-80260200	Enhancers	NHEK	skin
46	chr7:80259800-80260400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:80259800-80260400	Enhancers	Colon Smooth Muscle	Colon
48	chr7:80259800-80260600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:80259800-80260600	Enhancers	Osteobl	bone
50	chr7:80259800-80260800	Enhancers	Hela-S3	cervix

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