Variant report

Variant	nsv464286
Chromosome Location	chr7:4435801-4608174
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:918)
CpG islands
(count:549)
Chromatin interactive
region (count:18)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:4573177-4573308	K562	blood:	n/a	n/a
2	ARID3A	chr7:4446065-4446132	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:4601500-4601710	K562	blood:	n/a	n/a
4	ARID3A	chr7:4476207-4476541	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:4456113-4456402	K562	blood:	n/a	n/a
6	ATF2	chr7:4540407-4540709	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:4539804-4540066	HepG2	liver:	n/a	n/a
8	BHLHE40	chr7:4456107-4456375	K562	blood:	n/a	n/a
9	BRCA1	chr7:4519369-4519376	HepG2	liver:	n/a	n/a
10	CBX3	chr7:4523526-4523869	K562	blood:	n/a	n/a
11	CBX3	chr7:4539569-4539857	K562	blood:	n/a	n/a
12	CBX3	chr7:4523514-4523852	K562	blood:	n/a	n/a
13	CBX3	chr7:4539559-4539829	K562	blood:	n/a	n/a
14	CBX3	chr7:4592673-4592898	K562	blood:	n/a	n/a
15	CCNT2	chr7:4456019-4456350	K562	blood:	n/a	n/a
16	CEBPB	chr7:4435786-4436017	HepG2	liver:	n/a	chr7:4435872-4435883
17	CEBPB	chr7:4533851-4534051	A549	lung:	n/a	chr7:4533904-4533915
18	CEBPB	chr7:4585045-4585090	A549	lung:	n/a	n/a
19	CEBPB	chr7:4606356-4606720	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:4606342-4606723	K562	blood:	n/a	n/a
21	CEBPB	chr7:4510903-4511140	IMR90	lung:	n/a	chr7:4511007-4511018
22	CEBPB	chr7:4606355-4606641	K562	blood:	n/a	n/a
23	CEBPB	chr7:4606363-4606718	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:4606368-4606733	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:4526970-4527129	H1-hESC	embryonic stem cell:	n/a	chr7:4527026-4527037
26	CEBPB	chr7:4533869-4534052	IMR90	lung:	n/a	chr7:4533904-4533915
27	CEBPB	chr7:4510906-4511100	A549	lung:	n/a	chr7:4511007-4511018
28	CEBPB	chr7:4526879-4527083	K562	blood:	n/a	chr7:4527026-4527037
29	CEBPB	chr7:4606331-4606697	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr7:4606356-4606718	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr7:4533824-4534026	K562	blood:	n/a	chr7:4533904-4533915
32	CEBPB	chr7:4445955-4446291	HepG2	liver:	n/a	chr7:4446089-4446100
33	CEBPB	chr7:4526888-4527175	HepG2	liver:	n/a	chr7:4527026-4527037
34	CEBPB	chr7:4606335-4606705	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr7:4606287-4606701	A549	lung:	n/a	n/a
36	CEBPB	chr7:4526839-4527196	MCF-7	breast:	n/a	chr7:4527026-4527037
37	CEBPB	chr7:4606920-4607086	HepG2	liver:	n/a	chr7:4606937-4606948
38	CEBPB	chr7:4606357-4606697	A549	lung:	n/a	n/a
39	CEBPB	chr7:4606462-4606612	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:4562189-4562372	K562	blood:	n/a	chr7:4562300-4562311
41	CEBPB	chr7:4516153-4516177	HepG2	liver:	n/a	chr7:4516157-4516168
42	CEBPB	chr7:4510880-4511093	HepG2	liver:	n/a	chr7:4511007-4511018
43	CEBPB	chr7:4606348-4606704	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:4562197-4562343	HepG2	liver:	n/a	chr7:4562300-4562311
45	CEBPB	chr7:4526863-4527183	MCF-7	breast:	n/a	chr7:4527026-4527037
46	CEBPB	chr7:4584957-4585000	HepG2	liver:	n/a	chr7:4584972-4584983
47	CEBPB	chr7:4606365-4606717	A549	lung:	n/a	n/a
48	CEBPB	chr7:4526882-4527110	IMR90	lung:	n/a	chr7:4527026-4527037
49	CEBPB	chr7:4510874-4511113	K562	blood:	n/a	chr7:4511007-4511018
50	CEBPB	chr7:4526987-4527171	A549	lung:	n/a	chr7:4527026-4527037

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4456119-4456169	SK-N-SH_RA	brain:	n/a
2	chr7:4456396-4456446	MCF10A-Er-Src	breast:	n/a
3	chr7:4456396-4456446	U87	brain:	n/a
4	chr7:4573716-4573766	CMK	blood:	n/a
5	chr7:4456131-4456181	HCPEpiC	choroid plexus:	n/a
6	chr7:4536838-4536888	HNPCEpiC	eye:	n/a
7	chr7:4536864-4536914	BJ	skin:	n/a
8	chr7:4573716-4573766	HIPEpiC	eye:	n/a
9	chr7:4573716-4573766	GM19239	blood:	n/a
10	chr7:4456403-4456453	HNPCEpiC	eye:	n/a
11	chr7:4456403-4456453	HCM	heart:	n/a
12	chr7:4456341-4456391	SK-N-SH	brain:	n/a
13	chr7:4456131-4456181	AoSMC	blood vessel:	n/a
14	chr7:4536838-4536888	SK-N-SH_RA	brain:	n/a
15	chr7:4573535-4573585	HMEC	breast:	n/a
16	chr7:4536864-4536914	ECC-1	luminal epithelium:	n/a
17	chr7:4456131-4456181	IMR90	lung:	fetal
18	chr7:4456396-4456446	SK-N-SH_RA	brain:	n/a
19	chr7:4456119-4456169	AG09319	gingival:	n/a
20	chr7:4456341-4456391	HMEC	breast:	n/a
21	chr7:4573716-4573766	HNPCEpiC	eye:	n/a
22	chr7:4573716-4573766	AG10803	skin:	n/a
23	chr7:4456341-4456391	MCF10A-Er-Src	breast:	n/a
24	chr7:4573716-4573766	AG04449	skin:	fetal
25	chr7:4456396-4456446	PANC-1	pancreas:	n/a
26	chr7:4456119-4456169	HRCEpiC	kidney:	n/a
27	chr7:4536838-4536888	AG09309	skin:	n/a
28	chr7:4536838-4536888	Jurkat	blood:	n/a
29	chr7:4456341-4456391	SAEC	small airway:	n/a
30	chr7:4536838-4536888	NHBE	bronchial:	n/a
31	chr7:4573535-4573585	GM12878	blood:	n/a
32	chr7:4456403-4456453	Hela-S3	cervix:	n/a
33	chr7:4536864-4536914	AG09309	skin:	n/a
34	chr7:4456341-4456391	CMK	blood:	n/a
35	chr7:4573716-4573766	Jurkat	blood:	n/a
36	chr7:4456403-4456453	HCT-116	colon:	n/a
37	chr7:4536838-4536888	HL-60	blood:	n/a
38	chr7:4573535-4573585	Caco-2	colon:	n/a
39	chr7:4573535-4573585	HCM	heart:	n/a
40	chr7:4536864-4536914	HEK293	kidney:	embryo
41	chr7:4573716-4573766	AoSMC	blood vessel:	n/a
42	chr7:4456119-4456169	SKMC	muscle:	n/a
43	chr7:4456131-4456181	A549	lung:	n/a
44	chr7:4573535-4573585	ECC-1	luminal epithelium:	n/a
45	chr7:4573716-4573766	AG09309	skin:	n/a
46	chr7:4456341-4456391	HCT-116	colon:	n/a
47	chr7:4456396-4456446	HCT-116	colon:	n/a
48	chr7:4536864-4536914	Caco-2	colon:	n/a
49	chr7:4456131-4456181	NT2-D1	testis:	n/a
50	chr7:4573716-4573766	SK-N-SH	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4195210..4197944-chr7:4502921..4505536,2	MCF-7	breast:
2	chr20:52556259..52556926-chr7:4599215..4599761,2	MCF-7	breast:
3	chr7:4601107..4601677-chr7:4670928..4671456,2	MCF-7	breast:
4	chr7:4419960..4422829-chr7:4435237..4437889,2	MCF-7	breast:
5	chr7:4551212..4552814-chr7:4554906..4557306,2	K562	blood:
6	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
7	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
8	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
9	chr17:57920568..57922934-chr7:4466757..4469576,2	MCF-7	breast:
10	chr15:101629167..101629860-chr7:4485245..4486227,2	MCF-7	breast:
11	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
12	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
13	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
14	chr7:4401235..4402088-chr7:4518606..4519411,2	MCF-7	breast:
15	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
16	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
17	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
18	chr7:4074370..4074950-chr7:4518765..4519624,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXK1-1	chr7:4515791-4518319	XLOC_005972
2	lnc-RADIL-3	chr7:4452562-4452778	XLOC_006344
3	lnc-SDK1-1	chr7:4482317-4482707	l_3355_chr7:4440443-4482707_testes
4	lnc-FOXK1-1	chr7:4473994-4474153	XLOC_005972
5	lnc-RADIL-3	chr7:4455727-4456136	XLOC_006344
6	lnc-RADIL-4	chr7:4513174-4513309	NONHSAT118863
7	lnc-RADIL-4	chr7:4509330-4509430	NONHSAT118863
8	lnc-SDK1-1	chr7:4440444-4440679	l_3355_chr7:4440443-4482707_testes
9	lnc-RADIL-5	chr7:4472597-4475543	NONHSAT118861

No data

Variant related genes	Relation type
CYP3A54P	TF binding region
CYP3A54P	CpG island
ENSG00000261809	chromatin interactions
ENSG00000236352	chromatin interactions
VEGFA	miRNA target sites

Extended variants
information (count: 3502 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3502 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558534978	chr7:4440559-4440560	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs563711012	chr7:4440563-4440564	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs528463347	chr7:4440590-4440591	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs370437896	chr7:4440592-4440593	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs565951646	chr7:4440603-4440604	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs534533319	chr7:4440614-4440615	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs75494363	chr7:4440632-4440633	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs201276424	chr7:4440664-4440665	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs1992836	chr7:4440678-4440679	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs540427728	chr7:4442801-4442802	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs553732216	chr7:4442827-4442828	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs573772004	chr7:4442829-4442830	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs184486112	chr7:4442833-4442834	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs562541036	chr7:4442840-4442841	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs140756307	chr7:4442846-4442847	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs544980231	chr7:4442878-4442879	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs188880845	chr7:4442881-4442882	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs533499537	chr7:4442897-4442898	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs547261839	chr7:4442898-4442899	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs116603667	chr7:4442907-4442908	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs529465128	chr7:4442937-4442938	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs12111794	chr7:4442947-4442948	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs568978171	chr7:4442949-4442950	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs537860703	chr7:4442959-4442960	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs562121430	chr7:4442970-4442971	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs571306452	chr7:4443020-4443021	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs34700389	chr7:4443025-4443026	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs184027752	chr7:4443027-4443028	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs34725835	chr7:4443029-4443030	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs533883299	chr7:4443040-4443041	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs530752153	chr7:4443041-4443042	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs372509196	chr7:4443043-4443044	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs200776301	chr7:4443047-4443048	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs201845121	chr7:4443048-4443049	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs200032669	chr7:4443054-4443055	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs370609835	chr7:4443055-4443056	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs201005008	chr7:4443058-4443059	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs140499183	chr7:4443066-4443067	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs368775739	chr7:4443072-4443073	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs188526604	chr7:4443076-4443077	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
41	rs75136560	chr7:4443077-4443078	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
42	rs573782850	chr7:4443080-4443081	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
43	rs542772793	chr7:4443141-4443142	Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs534530568	chr7:4445601-4445602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs411394	chr7:4445609-4445610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113572103	chr7:4445622-4445623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559188039	chr7:4445626-4445627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543934303	chr7:4445647-4445648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563715283	chr7:4445652-4445653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs199830149	chr7:4445662-4445663	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4442800-4443200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:4442800-4443200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
3	chr7:4445600-4446600	Enhancers	HepG2	liver
4	chr7:4446200-4446600	Enhancers	Esophagus	oesophagus
5	chr7:4452400-4452800	Enhancers	Fetal Brain Male	brain
6	chr7:4452800-4456000	Weak transcription	Fetal Brain Male	brain
7	chr7:4455000-4457600	Enhancers	Fetal Intestine Small	intestine
8	chr7:4455400-4455800	Enhancers	Duodenum Mucosa	Duodenum
9	chr7:4455600-4455800	Enhancers	Brain Substantia Nigra	brain
10	chr7:4455600-4455800	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr7:4455600-4455800	Enhancers	Fetal Intestine Large	intestine
12	chr7:4455600-4456600	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr7:4455800-4456000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:4455800-4456000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr7:4455800-4456000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr7:4455800-4456000	Active TSS	Adipose Nuclei	Adipose
17	chr7:4455800-4456000	Flanking Active TSS	Duodenum Mucosa	Duodenum
18	chr7:4455800-4456000	Active TSS	Fetal Brain Female	brain
19	chr7:4455800-4456000	Flanking Active TSS	Fetal Intestine Large	intestine
20	chr7:4455800-4456000	Enhancers	Fetal Stomach	stomach
21	chr7:4455800-4456000	Enhancers	HepG2	liver
22	chr7:4455800-4456200	Active TSS	Aorta	Aorta
23	chr7:4455800-4456200	Active TSS	Brain Germinal Matrix	brain
24	chr7:4455800-4456200	Flanking Active TSS	Brain Substantia Nigra	brain
25	chr7:4455800-4456200	Active TSS	Fetal Lung	lung
26	chr7:4455800-4456400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:4455800-4456400	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr7:4455800-4456400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:4455800-4456400	Active TSS	Brain Hippocampus Middle	brain
30	chr7:4455800-4456400	Active TSS	Colon Smooth Muscle	Colon
31	chr7:4455800-4456400	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr7:4455800-4456400	Active TSS	A549	lung
33	chr7:4455800-4456600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:4455800-4456600	Active TSS	Brain Angular Gyrus	brain
35	chr7:4455800-4456600	Active TSS	Brain Anterior Caudate	brain
36	chr7:4455800-4456600	Active TSS	Brain Cingulate Gyrus	brain
37	chr7:4455800-4456600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr7:4455800-4456600	Active TSS	Stomach Mucosa	stomach
39	chr7:4455800-4456600	Active TSS	Stomach Smooth Muscle	stomach
40	chr7:4456000-4456200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:4456000-4456200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr7:4456000-4456200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr7:4456000-4456400	Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr7:4456000-4456400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr7:4456000-4456400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr7:4456000-4456400	Flanking Active TSS	Adipose Nuclei	Adipose
47	chr7:4456000-4456400	Flanking Active TSS	Fetal Brain Female	brain
48	chr7:4456000-4456400	Active TSS	Fetal Intestine Large	intestine
49	chr7:4456000-4456400	Enhancers	Fetal Muscle Trunk	muscle
50	chr7:4456000-4456400	Flanking Active TSS	Fetal Stomach	stomach

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