Variant report

Variant	nsv536638
Chromosome Location	chr3:89064073-89188335
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	chr3:89148161-89148488	HepG2	liver:	n/a	chr3:89148187-89148203 chr3:89148186-89148202
2	BACH1	chr3:89181076-89181309	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:89163694-89164008	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr3:89163784-89164066	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr3:89117092-89117290	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr3:89088103-89088358	A549	lung:	n/a	chr3:89088215-89088226
7	CEBPB	chr3:89088062-89088315	Hela-S3	cervix:	n/a	chr3:89088215-89088226
8	CEBPB	chr3:89088037-89088393	HepG2	liver:	n/a	chr3:89088215-89088226
9	CEBPB	chr3:89116973-89117300	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:89070832-89071184	IMR90	lung:	n/a	n/a
11	CEBPB	chr3:89081532-89081767	ECC-1	luminal epithelium:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
12	CEBPB	chr3:89156348-89156954	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:89088051-89088408	IMR90	lung:	n/a	chr3:89088215-89088226
14	CEBPB	chr3:89088054-89088386	H1-hESC	embryonic stem cell:	n/a	chr3:89088215-89088226
15	CEBPB	chr3:89081525-89081839	IMR90	lung:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
16	CEBPB	chr3:89074310-89074735	ECC-1	luminal epithelium:	n/a	chr3:89074330-89074343 chr3:89074332-89074343 chr3:89074330-89074343 chr3:89074332-89074343
17	CEBPB	chr3:89081560-89081809	HepG2	liver:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
18	CEBPB	chr3:89074376-89074717	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:89105427-89105685	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:89163835-89164403	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:89074405-89074757	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr3:89099791-89099870	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:89096183-89096427	HepG2	liver:	n/a	chr3:89096325-89096342
24	CHD2	chr3:89163393-89164131	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr3:89163735-89163967	HepG2	liver:	n/a	n/a
26	CHD2	chr3:89156526-89157194	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr3:89156893-89157090	HepG2	liver:	n/a	n/a
28	CREB1	chr3:89156643-89156888	A549	lung:	n/a	n/a
29	CTBP2	chr3:89163541-89164197	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr3:89156640-89156790	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr3:89148240-89148390	HVMF	connective:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
32	CTCF	chr3:89169760-89169910	HCPEpiC	choroid plexus:	n/a	chr3:89169873-89169891 chr3:89169868-89169889
33	CTCF	chr3:89163440-89163590	GM12869	blood:	n/a	n/a
34	CTCF	chr3:89098400-89098550	GM12875	blood:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
35	CTCF	chr3:89163860-89164010	SAEC	small airway:	n/a	chr3:89163918-89163934
36	CTCF	chr3:89148260-89148410	NHEK	skin:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
37	CTCF	chr3:89163454-89164116	MCF-7	breast:	n/a	chr3:89163918-89163934 chr3:89163657-89163670 chr3:89163655-89163673 chr3:89163811-89163824
38	CTCF	chr3:89148260-89148410	HUVEC	blood vessel:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
39	CTCF	chr3:89163808-89164042	LNCaP	prostate:	n/a	chr3:89163918-89163934 chr3:89163811-89163824
40	CTCF	chr3:89148192-89148482	GM10266	blood:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
41	CTCF	chr3:89163840-89163990	HepG2	liver:	n/a	chr3:89163918-89163934
42	CTCF	chr3:89163860-89164010	AG09309	skin:	n/a	chr3:89163918-89163934
43	CTCF	chr3:89163840-89163990	GM12801	blood:	n/a	chr3:89163918-89163934
44	CTCF	chr3:89148240-89148390	GM12801	blood:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
45	CTCF	chr3:89163840-89163990	HRPEpiC	eye:	n/a	chr3:89163918-89163934
46	CTCF	chr3:89148200-89148350	WI-38	lung:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
47	CTCF	chr3:89148220-89148370	HCFaa	heart:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
48	CTCF	chr3:89148209-89148463	A549	lung:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
49	CTCF	chr3:89163699-89164036	HepG2	liver:	n/a	chr3:89163918-89163934 chr3:89163811-89163824
50	CTCF	chr3:89163480-89163630	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:89156568-89156618	HEK293	kidney:	embryo
2	chr3:89164223-89164273	A549	lung:	n/a
3	chr3:89156568-89156618	HEK293	kidney:	embryo
4	chr3:89164223-89164273	A549	lung:	n/a
5	chr3:89163702-89163752	CMK	blood:	n/a
6	chr3:89156071-89156121	ovcar-3	ovarian:	n/a
7	chr3:89156071-89156121	SKMC	muscle:	n/a
8	chr3:89164038-89164088	NHBE	bronchial:	n/a
9	chr3:89156568-89156618	HCF	heart:	n/a
10	chr3:89163702-89163752	PrEC	prostate:	n/a
11	chr3:89164223-89164273	IMR90	lung:	fetal
12	chr3:89164038-89164088	AG10803	skin:	n/a
13	chr3:89163702-89163752	HCF	heart:	n/a
14	chr3:89156568-89156618	AG10803	skin:	n/a
15	chr3:89156676-89156726	BJ	skin:	n/a
16	chr3:89156830-89156880	GM06990	blood:	n/a
17	chr3:89156118-89156168	HCPEpiC	choroid plexus:	n/a
18	chr3:89097455-89097505	HAEpiC	amniotic membrane:	n/a
19	chr3:89156568-89156618	NHDF-neo	bronchial:	n/a
20	chr3:89163804-89163854	IMR90	lung:	fetal
21	chr3:89156830-89156880	SAEC	small airway:	n/a
22	chr3:89157002-89157052	GM12891	blood:	n/a
23	chr3:89164223-89164273	SKMC	muscle:	n/a
24	chr3:89164038-89164088	GM12892	blood:	n/a
25	chr3:89164038-89164088	GM06990	blood:	n/a
26	chr3:89156071-89156121	SK-N-SH_RA	brain:	n/a
27	chr3:89156676-89156726	NB4	blood:	n/a
28	chr3:89097455-89097505	Hepatocyte	liver:	n/a
29	chr3:89156676-89156726	GM12878	blood:	n/a
30	chr3:89157002-89157052	AG04449	skin:	fetal
31	chr3:89164038-89164088	Caco-2	colon:	n/a
32	chr3:89157002-89157052	HEK293	kidney:	embryo
33	chr3:89156795-89156845	ECC-1	luminal epithelium:	n/a
34	chr3:89163702-89163752	NHBE	bronchial:	n/a
35	chr3:89156568-89156618	GM06990	blood:	n/a
36	chr3:89156676-89156726	PrEC	prostate:	n/a
37	chr3:89156795-89156845	PANC-1	pancreas:	n/a
38	chr3:89156071-89156121	PFSK-1	brain:	n/a
39	chr3:89156676-89156726	HCF	heart:	n/a
40	chr3:89156676-89156726	HRE	kidney:	n/a
41	chr3:89156478-89156528	HRE	kidney:	n/a
42	chr3:89156568-89156618	AG04450	lung:	fetal
43	chr3:89164223-89164273	GM19239	blood:	n/a
44	chr3:89156830-89156880	NHBE	bronchial:	n/a
45	chr3:89156478-89156528	ProgFib	skin:	n/a
46	chr3:89164038-89164088	AG04449	skin:	fetal
47	chr3:89164223-89164273	AG09319	gingival:	n/a
48	chr3:89164038-89164088	Hela-S3	cervix:	n/a
49	chr3:89163702-89163752	MCF-7	breast:	n/a
50	chr3:89097455-89097505	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:88268096..88268898-chr3:89163502..89164670,4	MCF-7	breast:
2	chr3:88252425..88253380-chr3:89147853..89148709,5	MCF-7	breast:
3	chr3:88268154..88268973-chr3:89148016..89148802,3	MCF-7	breast:
4	chr3:88690003..88690853-chr3:89163399..89164385,5	MCF-7	breast:
5	chr3:89163095..89164119-chr3:89900902..89901799,5	MCF-7	breast:
6	chr3:89179300..89181545-chr3:89184054..89185924,2	MCF-7	breast:
7	chr3:88252276..88253622-chr3:89163430..89164364,7	MCF-7	breast:
8	chr3:88252535..88253252-chr3:89163320..89163834,2	MCF-7	breast:
9	chr3:89163419..89163996-chr3:89576891..89577500,2	MCF-7	breast:
10	chr3:88268148..88268804-chr3:89147889..89148832,3	MCF-7	breast:
11	chr3:89147543..89148341-chr3:89900953..89901507,2	MCF-7	breast:
12	chr3:89179300..89181545-chr3:89184054..89185924,2	MCF-7	breast:
13	chr3:89158394..89160004-chr3:89161963..89163485,2	MCF-7	breast:
14	chr3:89158394..89160004-chr3:89161963..89163485,2	MCF-7	breast:
15	chr3:88669439..88670359-chr3:89148166..89148816,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGGBP1-2	chr3:89096592-89097584	NONHSAT090710

Variant related genes	Relation type
EPHA3	TF binding region
GAPDHP50	TF binding region
EPHA3	CpG island
GAPDHP50	CpG island

Extended variants
information (count: 3323 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3323 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577514907	chr3:89064105-89064106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575657929	chr3:89064128-89064129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543145170	chr3:89064152-89064153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116748571	chr3:89064195-89064196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189686702	chr3:89064206-89064207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546371736	chr3:89064220-89064221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140205018	chr3:89064249-89064250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182356248	chr3:89064356-89064357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113620711	chr3:89064453-89064454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550172189	chr3:89064464-89064465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568877386	chr3:89064476-89064477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1566054	chr3:89064488-89064489	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548296112	chr3:89064492-89064493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7637489	chr3:89064495-89064496	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs535249218	chr3:89064499-89064500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145825037	chr3:89064569-89064570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75740779	chr3:89064570-89064571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539296771	chr3:89064588-89064589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111587234	chr3:89064590-89064591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186668676	chr3:89064618-89064619	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575640227	chr3:89064623-89064624	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368350988	chr3:89064624-89064625	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542632149	chr3:89064631-89064632	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561464852	chr3:89064646-89064647	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7626049	chr3:89064651-89064652	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs540043386	chr3:89064668-89064669	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371325142	chr3:89064704-89064705	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564699033	chr3:89064767-89064768	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532168551	chr3:89064807-89064808	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550509807	chr3:89064822-89064823	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200478449	chr3:89064851-89064852	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562619769	chr3:89064867-89064868	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541332319	chr3:89064875-89064876	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77951375	chr3:89064925-89064926	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547842993	chr3:89064928-89064929	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9867839	chr3:89064937-89064938	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs115502571	chr3:89064939-89064940	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367996267	chr3:89064964-89064965	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547224055	chr3:89064965-89064966	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79819698	chr3:89064989-89064990	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539229818	chr3:89064990-89064991	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565029532	chr3:89065036-89065037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557662213	chr3:89065038-89065039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569431709	chr3:89065060-89065061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536663269	chr3:89065083-89065084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193213628	chr3:89065104-89065105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201033553	chr3:89065110-89065111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115007363	chr3:89065168-89065169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1496514	chr3:89065177-89065178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs558624834	chr3:89065178-89065179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	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
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	21829676	CNVD
Lung cancer	19547694	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	19651600	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:89061800-89070600	Weak transcription	HMEC	breast
2	chr3:89063200-89064800	Enhancers	Fetal Brain Male	brain
3	chr3:89063600-89064400	Enhancers	Fetal Brain Female	brain
4	chr3:89064600-89065000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:89065400-89067400	Enhancers	Fetal Lung	lung
6	chr3:89068800-89069000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:89068800-89069200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:89069000-89074400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:89069200-89071000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:89070600-89071800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:89070600-89071800	Enhancers	HMEC	breast
12	chr3:89070600-89071800	Enhancers	NHDF-Ad	bronchial
13	chr3:89070600-89071800	Enhancers	Osteobl	bone
14	chr3:89070600-89072000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:89070800-89071200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr3:89070800-89071200	Enhancers	NH-A	brain
17	chr3:89070800-89071600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:89070800-89071800	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr3:89071000-89071200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr3:89071000-89071800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:89071000-89071800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr3:89071000-89072000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:89071200-89073800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:89071200-89073800	Weak transcription	NH-A	brain
25	chr3:89071800-89073200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr3:89071800-89073800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr3:89071800-89073800	Weak transcription	NHDF-Ad	bronchial
28	chr3:89071800-89074000	Weak transcription	Osteobl	bone
29	chr3:89071800-89074200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:89071800-89074200	Weak transcription	HMEC	breast
31	chr3:89072000-89073600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr3:89072000-89073800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:89073200-89074400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr3:89073600-89074000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:89073800-89074000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:89073800-89074200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:89073800-89074200	Enhancers	NH-A	brain
38	chr3:89073800-89074200	Enhancers	NHDF-Ad	bronchial
39	chr3:89073800-89074400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr3:89073800-89074600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:89074000-89074200	Enhancers	Osteobl	bone
42	chr3:89074000-89074400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr3:89074000-89074600	Enhancers	Brain Germinal Matrix	brain
44	chr3:89074000-89074800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr3:89074000-89074800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:89074200-89074400	Flanking Active TSS	Osteobl	bone
47	chr3:89074200-89074600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr3:89074200-89074600	Active TSS	Brain Substantia Nigra	brain
49	chr3:89074200-89074600	Enhancers	HMEC	breast
50	chr3:89074200-89074600	Active TSS	NH-A	brain

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