Variant report

Variant	nsv998460
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	chr3:89088054-89088386	H1-hESC	embryonic stem cell:	n/a	chr3:89088215-89088226
7	CEBPB	chr3:89070832-89071184	IMR90	lung:	n/a	n/a
8	CEBPB	chr3:89074405-89074757	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr3:89088103-89088358	A549	lung:	n/a	chr3:89088215-89088226
10	CEBPB	chr3:89116973-89117300	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:89074376-89074717	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:89088037-89088393	HepG2	liver:	n/a	chr3:89088215-89088226
13	CEBPB	chr3:89081560-89081809	HepG2	liver:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
14	CEBPB	chr3:89096183-89096427	HepG2	liver:	n/a	chr3:89096325-89096342
15	CEBPB	chr3:89156348-89156954	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr3:89088051-89088408	IMR90	lung:	n/a	chr3:89088215-89088226
18	CEBPB	chr3:89105427-89105685	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:89081525-89081839	IMR90	lung:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
20	CEBPB	chr3:89099791-89099870	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:89081532-89081767	ECC-1	luminal epithelium:	n/a	chr3:89081654-89081665 chr3:89081704-89081716 chr3:89081653-89081666
22	CEBPB	chr3:89163835-89164403	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:89088062-89088315	Hela-S3	cervix:	n/a	chr3:89088215-89088226
24	CHD2	chr3:89156893-89157090	HepG2	liver:	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	chr3:89163393-89164131	H1-hESC	embryonic stem cell:	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	chr3:89148244-89148415	H1-hESC	embryonic stem cell:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
31	CTCF	chr3:89163840-89163990	GM06990	blood:	n/a	chr3:89163918-89163934
32	CTCF	chr3:89098400-89098550	BJ	skin:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
33	CTCF	chr3:89098300-89098450	GM06990	blood:	n/a	n/a
34	CTCF	chr3:89098380-89098530	WERI-Rb-1	eye:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
35	CTCF	chr3:89148220-89148370	GM12868	blood:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
36	CTCF	chr3:89148240-89148390	HBMEC	blood vessel:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
37	CTCF	chr3:89156660-89156810	AG04449	skin:	n/a	n/a
38	CTCF	chr3:89098320-89098470	HRE	kidney:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
39	CTCF	chr3:89098416-89098420	GM19239	blood:	n/a	n/a
40	CTCF	chr3:89163840-89163990	BE2_C	brain:	n/a	chr3:89163918-89163934
41	CTCF	chr3:89163660-89163810	HMEC	breast:	n/a	n/a
42	CTCF	chr3:89098406-89098465	GM12891	blood:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
43	CTCF	chr3:89148260-89148410	GM12871	blood:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
44	CTCF	chr3:89098340-89098490	HCFaa	heart:	n/a	chr3:89098447-89098456 chr3:89098441-89098459
45	CTCF	chr3:89148220-89148370	HCFaa	heart:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
46	CTCF	chr3:89148260-89148410	GM12864	blood:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
47	CTCF	chr3:89163820-89163970	K562	blood:	n/a	chr3:89163918-89163934
48	CTCF	chr3:89169700-89169850	HCFaa	heart:	n/a	n/a
49	CTCF	chr3:89148240-89148390	HMEC	breast:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331
50	CTCF	chr3:89148260-89148410	HCM	heart:	n/a	chr3:89148319-89148327 chr3:89148314-89148332 chr3:89148309-89148330 chr3:89148315-89148331

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:89164038-89164088	BE2_C	brain:	n/a
2	chr3:89157002-89157052	SK-N-SH_RA	brain:	n/a
3	chr3:89156676-89156726	NH-A	brain:	n/a
4	chr3:89163702-89163752	HCF	heart:	n/a
5	chr3:89156478-89156528	AG10803	skin:	n/a
6	chr3:89156676-89156726	Jurkat	blood:	n/a
7	chr3:89164038-89164088	NT2-D1	testis:	n/a
8	chr3:89156568-89156618	HIPEpiC	eye:	n/a
9	chr3:89163804-89163854	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:89163804-89163854	AG04449	skin:	fetal
11	chr3:89156478-89156528	AG09309	skin:	n/a
12	chr3:89163702-89163752	T-47D	breast:	n/a
13	chr3:89097455-89097505	HCF	heart:	n/a
14	chr3:89156118-89156168	HRCEpiC	kidney:	n/a
15	chr3:89156478-89156528	HEEpiC	esophagus:	n/a
16	chr3:89164038-89164088	HRE	kidney:	n/a
17	chr3:89157002-89157052	ovcar-3	ovarian:	n/a
18	chr3:89156795-89156845	NH-A	brain:	n/a
19	chr3:89156795-89156845	MCF-7	breast:	n/a
20	chr3:89156568-89156618	HNPCEpiC	eye:	n/a
21	chr3:89163804-89163854	BJ	skin:	n/a
22	chr3:89163804-89163854	ECC-1	luminal epithelium:	n/a
23	chr3:89163804-89163854	ProgFib	skin:	n/a
24	chr3:89156830-89156880	LNCaP	prostate:	n/a
25	chr3:89156118-89156168	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:89156676-89156726	PrEC	prostate:	n/a
27	chr3:89156676-89156726	HRPEpiC	eye:	n/a
28	chr3:89156568-89156618	GM19239	blood:	n/a
29	chr3:89097455-89097505	A549	lung:	n/a
30	chr3:89156795-89156845	HCM	heart:	n/a
31	chr3:89156071-89156121	NT2-D1	testis:	n/a
32	chr3:89156676-89156726	NHDF-neo	bronchial:	n/a
33	chr3:89164223-89164273	ECC-1	luminal epithelium:	n/a
34	chr3:89156118-89156168	HCT-116	colon:	n/a
35	chr3:89156830-89156880	AG10803	skin:	n/a
36	chr3:89164223-89164273	HAEpiC	amniotic membrane:	n/a
37	chr3:89164223-89164273	SAEC	small airway:	n/a
38	chr3:89156568-89156618	MCF10A-Er-Src	breast:	n/a
39	chr3:89097455-89097505	HL-60	blood:	n/a
40	chr3:89156118-89156168	HNPCEpiC	eye:	n/a
41	chr3:89163804-89163854	ovcar-3	ovarian:	n/a
42	chr3:89163804-89163854	HIPEpiC	eye:	n/a
43	chr3:89164038-89164088	HPAEpiC	pulmonary alveolar:	n/a
44	chr3:89157002-89157052	SK-N-SH	brain:	n/a
45	chr3:89164038-89164088	HCPEpiC	choroid plexus:	n/a
46	chr3:89156830-89156880	AG09309	skin:	n/a
47	chr3:89156676-89156726	HL-60	blood:	n/a
48	chr3:89156478-89156528	AG04449	skin:	fetal
49	chr3:89156676-89156726	HEEpiC	esophagus:	n/a
50	chr3:89163702-89163752	GM06990	blood:	n/a

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