Variant report

Variant	nsv877037
Chromosome Location	chr3:80611818-80811252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:718)
CpG islands
(count:61)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:718 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:80667214-80667911	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:80782695-80783245	K562	blood:	n/a	n/a
3	ARID3A	chr3:80745362-80745831	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:80782752-80783150	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:80661433-80661978	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:80738119-80738207	HepG2	liver:	n/a	n/a
7	ATF1	chr3:80782701-80783197	K562	blood:	n/a	n/a
8	ATF3	chr3:80782952-80783204	K562	blood:	n/a	n/a
9	BACH1	chr3:80655575-80655582	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr3:80782656-80783250	K562	blood:	n/a	n/a
11	BHLHE40	chr3:80782752-80783188	HepG2	liver:	n/a	n/a
12	BRCA1	chr3:80805347-80805353	HepG2	liver:	n/a	n/a
13	CBX3	chr3:80782653-80782974	K562	blood:	n/a	n/a
14	CCNT2	chr3:80782710-80783028	K562	blood:	n/a	n/a
15	CCNT2	chr3:80721057-80721441	K562	blood:	n/a	n/a
16	CEBPB	chr3:80635551-80635792	MCF-7	breast:	n/a	n/a
17	CEBPB	chr3:80782661-80783114	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:80692621-80693004	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr3:80717097-80717280	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:80635512-80635838	IMR90	lung:	n/a	n/a
21	CEBPB	chr3:80745404-80745862	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:80799635-80800188	Hela-S3	cervix:	n/a	chr3:80799782-80799793
23	CEBPB	chr3:80790843-80791115	HepG2	liver:	n/a	chr3:80790948-80790959 chr3:80791016-80791028 chr3:80790967-80790980 chr3:80790968-80790979 chr3:80790947-80790960 chr3:80790967-80790980
24	CEBPB	chr3:80739874-80740195	IMR90	lung:	n/a	chr3:80740063-80740074 chr3:80740018-80740029 chr3:80740061-80740072 chr3:80740061-80740074
25	CEBPB	chr3:80692576-80693005	MCF-7	breast:	n/a	n/a
26	CEBPB	chr3:80692540-80693009	MCF-7	breast:	n/a	n/a
27	CEBPB	chr3:80799879-80800134	HepG2	liver:	n/a	n/a
28	CEBPB	chr3:80799876-80800190	K562	blood:	n/a	n/a
29	CEBPB	chr3:80635490-80635885	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr3:80692585-80692978	K562	blood:	n/a	n/a
31	CEBPB	chr3:80635532-80635865	A549	lung:	n/a	n/a
32	CEBPB	chr3:80667454-80667778	HepG2	liver:	n/a	n/a
33	CEBPB	chr3:80754710-80754924	IMR90	lung:	n/a	n/a
34	CEBPB	chr3:80692548-80692986	A549	lung:	n/a	n/a
35	CEBPB	chr3:80635592-80635726	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:80790892-80791124	A549	lung:	n/a	chr3:80790948-80790959 chr3:80791016-80791028 chr3:80790967-80790980 chr3:80790968-80790979 chr3:80790947-80790960 chr3:80790967-80790980
37	CEBPB	chr3:80692611-80692975	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:80692612-80692978	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr3:80739882-80740198	HepG2	liver:	n/a	chr3:80740063-80740074 chr3:80740018-80740029 chr3:80740061-80740072 chr3:80740061-80740074
40	CEBPB	chr3:80667486-80667705	HepG2	liver:	n/a	n/a
41	CEBPB	chr3:80782584-80783442	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:80754721-80754976	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr3:80790837-80791087	K562	blood:	n/a	chr3:80790948-80790959 chr3:80791016-80791028 chr3:80790967-80790980 chr3:80790968-80790979 chr3:80790947-80790960 chr3:80790967-80790980
44	CEBPB	chr3:80745508-80746034	MCF-7	breast:	n/a	n/a
45	CEBPB	chr3:80799930-80800138	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:80654642-80654882	IMR90	lung:	n/a	n/a
47	CEBPB	chr3:80692666-80692857	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:80782711-80782986	K562	blood:	n/a	n/a
49	CEBPB	chr3:80635515-80635812	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr3:80635487-80635815	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:80802625-80802675	ovcar-3	ovarian:	n/a
2	chr3:80802625-80802675	HCM	heart:	n/a
3	chr3:80802625-80802675	K562	blood:	n/a
4	chr3:80802625-80802675	GM12891	blood:	n/a
5	chr3:80802625-80802675	BE2_C	brain:	n/a
6	chr3:80802625-80802675	CMK	blood:	n/a
7	chr3:80802625-80802675	LNCaP	prostate:	n/a
8	chr3:80802625-80802675	NHBE	bronchial:	n/a
9	chr3:80802625-80802675	HRCEpiC	kidney:	n/a
10	chr3:80802625-80802675	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:80802625-80802675	NHDF-neo	bronchial:	n/a
12	chr3:80802625-80802675	GM12892	blood:	n/a
13	chr3:80802625-80802675	HRPEpiC	eye:	n/a
14	chr3:80802625-80802675	SK-N-SH_RA	brain:	n/a
15	chr3:80802625-80802675	SAEC	small airway:	n/a
16	chr3:80802625-80802675	A549	lung:	n/a
17	chr3:80802625-80802675	AG09309	skin:	n/a
18	chr3:80802625-80802675	AG04450	lung:	fetal
19	chr3:80802625-80802675	NH-A	brain:	n/a
20	chr3:80802625-80802675	GM12878	blood:	n/a
21	chr3:80802625-80802675	IMR90	lung:	fetal
22	chr3:80802625-80802675	H1-hESC	embryonic stem cell:	embryo
23	chr3:80802625-80802675	HAEpiC	amniotic membrane:	n/a
24	chr3:80802625-80802675	SK-N-MC	brain:	n/a
25	chr3:80802625-80802675	NT2-D1	testis:	n/a
26	chr3:80802625-80802675	PrEC	prostate:	n/a
27	chr3:80802625-80802675	T-47D	breast:	n/a
28	chr3:80802625-80802675	U87	brain:	n/a
29	chr3:80802625-80802675	HepG2	liver:	n/a
30	chr3:80802625-80802675	PFSK-1	brain:	n/a
31	chr3:80802625-80802675	NB4	blood:	n/a
32	chr3:80802625-80802675	BJ	skin:	n/a
33	chr3:80802625-80802675	HIPEpiC	eye:	n/a
34	chr3:80802625-80802675	HCF	heart:	n/a
35	chr3:80802625-80802675	HRE	kidney:	n/a
36	chr3:80802625-80802675	HUVEC	blood vessel:	n/a
37	chr3:80802625-80802675	SKMC	muscle:	n/a
38	chr3:80802625-80802675	RPTEC	kidney:	n/a
39	chr3:80802625-80802675	HEK293	kidney:	embryo
40	chr3:80802625-80802675	HL-60	blood:	n/a
41	chr3:80802625-80802675	SK-N-SH	brain:	n/a
42	chr3:80802625-80802675	Hela-S3	cervix:	n/a
43	chr3:80802625-80802675	AG04449	skin:	fetal
44	chr3:80802625-80802675	HCPEpiC	choroid plexus:	n/a
45	chr3:80802625-80802675	HEEpiC	esophagus:	n/a
46	chr3:80802625-80802675	AG10803	skin:	n/a
47	chr3:80802625-80802675	HCT-116	colon:	n/a
48	chr3:80802625-80802675	Hepatocyte	liver:	n/a
49	chr3:80802625-80802675	HMEC	breast:	n/a
50	chr3:80802625-80802675	AG09319	gingival:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:56707663..56711922-chr3:80675625..80678686,47	MCF-7	breast:
2	chr17:56734902..56738001-chr3:80677142..80678686,4	K562	blood:
3	chr17:56702140..56703748-chr3:80675685..80678645,2	MCF-7	breast:
4	chr3:80627129..80630105-chr3:80631762..80633274,2	MCF-7	breast:
5	chr3:80806849..80809276-chr3:81106708..81109686,2	MCF-7	breast:
6	chr17:56708809..56709539-chr3:80676642..80677684,6	Hela-S3	cervix:
7	chr3:80654997..80655872-chr3:80725776..80726345,3	MCF-7	breast:
8	chr17:56708399..56709680-chr3:80676622..80677717,127	MCF-7	breast:
9	chr17:56708416..56709700-chr3:80676622..80677685,55	HCT-116	colon:
10	chr17:56705518..56710413-chr3:80675622..80678686,101	MCF-7	breast:
11	chr3:80065925..80067779-chr3:80730870..80732420,2	MCF-7	breast:
12	chr3:80733806..80735603-chr3:80743494..80745970,2	K562	blood:
13	chr3:80636124..80636926-chr3:85151824..85152666,2	Hela-S3	cervix:
14	chr17:56654336..56655943-chr3:80677127..80678644,2	K562	blood:
15	chr3:80804545..80806056-chr3:80810607..80813486,2	K562	blood:
16	chr17:56708656..56709177-chr3:80677124..80677665,2	MCF-7	breast:
17	chr17:56707583..56710440-chr3:80675624..80678665,17	K562	blood:
18	chr17:56716338..56717980-chr3:80675665..80678624,2	MCF-7	breast:
19	chr3:80804545..80806056-chr3:80810607..80813486,2	K562	blood:
20	chr3:80627129..80630105-chr3:80631762..80633274,2	MCF-7	breast:
21	chr3:80575021..80575834-chr3:80725791..80726747,5	MCF-7	breast:
22	chr3:80654997..80655872-chr3:80725776..80726345,3	MCF-7	breast:
23	chr3:80733806..80735603-chr3:80743494..80745970,2	K562	blood:
24	chr17:56708616..56709587-chr3:80676624..80677684,14	NB4	blood:
25	chr17:56705485..56710914-chr3:80675644..80678685,20	K562	blood:
26	chr3:80634418..80636730-chr3:80639554..80641619,2	K562	blood:
27	chr17:56594883..56597200-chr3:80675665..80678626,2	K562	blood:
28	chr17:56704272..56706985-chr3:80675644..80677185,2	K562	blood:
29	chr3:80634418..80636730-chr3:80639554..80641619,2	K562	blood:
30	chr3:80810046..80811572-chr3:80815294..80817977,2	K562	blood:
31	chr17:56708636..56709461-chr3:80677123..80677664,11	MCF-7	breast:
32	chr17:56736245..56738976-chr3:80677124..80678684,2	MCF-7	breast:
33	chr17:56703997..56706897-chr3:80675625..80677164,2	MCF-7	breast:
34	chr17:56708245..56709624-chr3:80676622..80677686,211	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GBE1-5	chr3:80810609-80810724	XLOC_003167
2	lnc-GBE1-5	chr3:80810193-80810356	XLOC_003167

No data

Variant related genes	Relation type
ENSG00000242781	TF binding region
ENSG00000242781	CpG island
ENSG00000212195	chromatin interactions
ENSG00000266826	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000264672	chromatin interactions
ENSG00000108389	chromatin interactions

Extended variants
information (count: 2624 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73851777	chr3:80630083-80630084	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs66826901	chr3:80630085-80630086	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs139014971	chr3:80630123-80630124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149913513	chr3:80630144-80630145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575019024	chr3:80630149-80630150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184524771	chr3:80630155-80630156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563943464	chr3:80630162-80630163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569537812	chr3:80630180-80630181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532870897	chr3:80630203-80630204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545775142	chr3:80630232-80630233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538193989	chr3:80630256-80630257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6548719	chr3:80630259-80630260	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs139189498	chr3:80630285-80630286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528189065	chr3:80630313-80630314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375024577	chr3:80630336-80630337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548304535	chr3:80630344-80630345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188970934	chr3:80630380-80630381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530763083	chr3:80630399-80630400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553402101	chr3:80632009-80632010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537543231	chr3:80632010-80632011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551127945	chr3:80632014-80632015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571034627	chr3:80632050-80632051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540011985	chr3:80632074-80632075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186309738	chr3:80632093-80632094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573442868	chr3:80632118-80632119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538508952	chr3:80632159-80632160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114676062	chr3:80632173-80632174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532454868	chr3:80632183-80632184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190709032	chr3:80632184-80632185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539197464	chr3:80635200-80635201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35201466	chr3:80635204-80635205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576132140	chr3:80635221-80635222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149961926	chr3:80635309-80635310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531815329	chr3:80635381-80635382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183990709	chr3:80635411-80635412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188329188	chr3:80635413-80635414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117133125	chr3:80635418-80635419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs180748638	chr3:80635457-80635458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567301030	chr3:80635549-80635550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188686432	chr3:80655433-80655434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574992190	chr3:80655440-80655441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546628571	chr3:80655444-80655445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372783068	chr3:80655521-80655522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547687066	chr3:80655556-80655557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9827895	chr3:80655607-80655608	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs535802353	chr3:80655624-80655625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149076328	chr3:80655648-80655649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73851780	chr3:80655688-80655689	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs539006373	chr3:80655735-80655736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2372502	chr3:80655763-80655764	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:80630000-80630400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr3:80630000-80630400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:80632000-80632200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr3:80635200-80635600	Enhancers	Pancreas	Pancrea
5	chr3:80655400-80656400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:80655400-80656600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr3:80655600-80656400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:80655600-80656600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:80655600-80656800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:80655800-80656400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:80655800-80656600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr3:80656600-80661600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr3:80661200-80663000	Enhancers	HepG2	liver
14	chr3:80661400-80661800	Enhancers	Fetal Intestine Large	intestine
15	chr3:80661600-80662000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr3:80662000-80662200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:80662200-80662600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr3:80663000-80666800	Weak transcription	HepG2	liver
19	chr3:80666800-80667000	Enhancers	HepG2	liver
20	chr3:80667000-80667400	Weak transcription	HepG2	liver
21	chr3:80667400-80668600	Enhancers	HUVEC	blood vessel
22	chr3:80667400-80668800	Enhancers	HepG2	liver
23	chr3:80667800-80668600	Enhancers	Fetal Intestine Large	intestine
24	chr3:80681600-80682000	Enhancers	Brain Germinal Matrix	brain
25	chr3:80683800-80684200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:80684000-80684400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr3:80684800-80685200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr3:80692600-80693000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr3:80703600-80705600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr3:80704000-80705000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr3:80704400-80704800	ZNF genes & repeats	Osteobl	bone
32	chr3:80704600-80705000	Enhancers	Brain Germinal Matrix	brain
33	chr3:80708200-80708600	Active TSS	Gastric	stomach
34	chr3:80717200-80718200	ZNF genes & repeats	Fetal Intestine Small	intestine
35	chr3:80717400-80718600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
36	chr3:80717600-80717800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
37	chr3:80717600-80717800	ZNF genes & repeats	Placenta	Placenta
38	chr3:80717800-80718200	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr3:80717800-80718400	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr3:80717800-80718600	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr3:80718200-80718400	Active TSS	Duodenum Mucosa	Duodenum
42	chr3:80718200-80718600	Enhancers	HepG2	liver
43	chr3:80718400-80718600	Flanking Active TSS	Duodenum Mucosa	Duodenum
44	chr3:80718600-80718800	Active TSS	Duodenum Mucosa	Duodenum
45	chr3:80724400-80724600	Enhancers	Fetal Brain Male	brain
46	chr3:80724600-80725000	Enhancers	Fetal Brain Female	brain
47	chr3:80725200-80725600	Enhancers	Fetal Brain Female	brain
48	chr3:80725800-80726000	Enhancers	Fetal Brain Male	brain
49	chr3:80726600-80727600	Enhancers	HUVEC	blood vessel
50	chr3:80727000-80727600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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