Variant report

Variant	nsv876995
Chromosome Location	chr3:76015252-76114539
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	ATF2	chr3:76092810-76093431	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:76092805-76093300	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr3:76091734-76092099	GM12878	blood:	n/a	n/a
4	BATF	chr3:76091730-76092060	GM12878	blood:	n/a	n/a
5	BCL11A	chr3:76091772-76091983	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:76091692-76092106	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:76094241-76094379	GM12878	blood:	n/a	n/a
8	BRCA1	chr3:76092875-76093639	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:76023773-76024060	A549	lung:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
10	CEBPB	chr3:76093689-76094128	IMR90	lung:	n/a	n/a
11	CEBPB	chr3:76093872-76094087	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:76034636-76034981	K562	blood:	n/a	chr3:76034793-76034804
13	CEBPB	chr3:76023890-76023921	H1-hESC	embryonic stem cell:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
14	CEBPB	chr3:76025393-76025671	HepG2	liver:	n/a	chr3:76025511-76025522
15	CEBPB	chr3:76023733-76024088	HepG2	liver:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
16	CEBPB	chr3:76092893-76093312	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:76034619-76034978	A549	lung:	n/a	chr3:76034793-76034804
18	CEBPB	chr3:76034701-76034915	H1-hESC	embryonic stem cell:	n/a	chr3:76034793-76034804
19	CEBPB	chr3:76034632-76034971	IMR90	lung:	n/a	chr3:76034793-76034804
20	CEBPB	chr3:76034609-76034974	HepG2	liver:	n/a	chr3:76034793-76034804
21	CEBPB	chr3:76023734-76024093	IMR90	lung:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
22	CHD1	chr3:76089070-76089144	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr3:76088184-76088476	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr3:76088171-76088769	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr3:76092684-76093435	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr3:76092854-76093434	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTBP2	chr3:76092954-76093387	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr3:76094280-76094430	GM06990	blood:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
29	CTCF	chr3:76073820-76073970	HVMF	connective:	n/a	n/a
30	CTCF	chr3:76094200-76094350	HepG2	liver:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
31	CTCF	chr3:76094267-76094416	GM13976	blood:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
32	CTCF	chr3:76073940-76074090	HMEC	breast:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
33	CTCF	chr3:76073920-76074070	AG04450	lung:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
34	CTCF	chr3:76082615-76082674	GM13976	blood:	n/a	n/a
35	CTCF	chr3:76073920-76074070	NB4	blood:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
36	CTCF	chr3:76094138-76094572	IMR90	lung:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
37	CTCF	chr3:76073920-76074070	NHEK	skin:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
38	CTCF	chr3:76094136-76094528	GM12878	blood:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
39	CTCF	chr3:76038309-76038364	GM10248	blood:	n/a	n/a
40	CTCF	chr3:76094220-76094370	BJ	skin:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
41	CTCF	chr3:76094280-76094430	Hela-S3	cervix:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
42	CTCF	chr3:76073940-76074090	AG09319	gingival:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
43	CTCF	chr3:76094280-76094430	GM12864	blood:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
44	CTCF	chr3:76073919-76074054	GM13977	blood:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
45	CTCF	chr3:76094220-76094370	Caco-2	colon:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
46	CTCF	chr3:76073865-76074108	H1-hESC	embryonic stem cell:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
47	CTCF	chr3:76094260-76094410	HRE	kidney:	n/a	chr3:76094319-76094337 chr3:76094314-76094335
48	CTCF	chr3:76073920-76074070	HCM	heart:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
49	CTCF	chr3:76094360-76094510	HVMF	connective:	n/a	n/a
50	CTCF	chr3:76094240-76094390	HPAF	blood vessel:	n/a	chr3:76094319-76094337 chr3:76094314-76094335

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:76062791-76062841	U87	brain:	n/a
2	chr3:76087918-76087968	AoSMC	blood vessel:	n/a
3	chr3:76063500-76063550	Caco-2	colon:	n/a
4	chr3:76087918-76087968	HepG2	liver:	n/a
5	chr3:76076212-76076262	PFSK-1	brain:	n/a
6	chr3:76062791-76062841	HAEpiC	amniotic membrane:	n/a
7	chr3:76076212-76076262	AG09319	gingival:	n/a
8	chr3:76076212-76076262	NT2-D1	testis:	n/a
9	chr3:76062325-76062375	GM12878	blood:	n/a
10	chr3:76063500-76063550	SK-N-SH_RA	brain:	n/a
11	chr3:76062325-76062375	NHDF-neo	bronchial:	n/a
12	chr3:76087918-76087968	GM12892	blood:	n/a
13	chr3:76112323-76112373	SAEC	small airway:	n/a
14	chr3:76087918-76087968	K562	blood:	n/a
15	chr3:76112323-76112373	A549	lung:	n/a
16	chr3:76062791-76062841	Caco-2	colon:	n/a
17	chr3:76062325-76062375	HCM	heart:	n/a
18	chr3:76062325-76062375	AoSMC	blood vessel:	n/a
19	chr3:76063500-76063550	SK-N-MC	brain:	n/a
20	chr3:76062791-76062841	AG04449	skin:	fetal
21	chr3:76112323-76112373	BE2_C	brain:	n/a
22	chr3:76076212-76076262	LNCaP	prostate:	n/a
23	chr3:76063343-76063393	SAEC	small airway:	n/a
24	chr3:76076212-76076262	HEEpiC	esophagus:	n/a
25	chr3:76112323-76112373	HL-60	blood:	n/a
26	chr3:76063343-76063393	AG09309	skin:	n/a
27	chr3:76062325-76062375	IMR90	lung:	fetal
28	chr3:76062325-76062375	RPTEC	kidney:	n/a
29	chr3:76063500-76063550	PANC-1	pancreas:	n/a
30	chr3:76063500-76063550	Hela-S3	cervix:	n/a
31	chr3:76076212-76076262	HAEpiC	amniotic membrane:	n/a
32	chr3:76062791-76062841	ECC-1	luminal epithelium:	n/a
33	chr3:76063343-76063393	HepG2	liver:	n/a
34	chr3:76076212-76076262	T-47D	breast:	n/a
35	chr3:76087918-76087968	SAEC	small airway:	n/a
36	chr3:76063500-76063550	GM19239	blood:	n/a
37	chr3:76062791-76062841	NB4	blood:	n/a
38	chr3:76087918-76087968	BJ	skin:	n/a
39	chr3:76062791-76062841	AoSMC	blood vessel:	n/a
40	chr3:76062791-76062841	Hepatocyte	liver:	n/a
41	chr3:76063343-76063393	SK-N-SH_RA	brain:	n/a
42	chr3:76063343-76063393	SK-N-MC	brain:	n/a
43	chr3:76062325-76062375	ProgFib	skin:	n/a
44	chr3:76076212-76076262	AG04449	skin:	fetal
45	chr3:76063343-76063393	HRCEpiC	kidney:	n/a
46	chr3:76063500-76063550	GM12891	blood:	n/a
47	chr3:76062791-76062841	SK-N-MC	brain:	n/a
48	chr3:76062791-76062841	PrEC	prostate:	n/a
49	chr3:76087918-76087968	NHBE	bronchial:	n/a
50	chr3:76062791-76062841	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:76073881..76074768-chr3:76093884..76094767,3	MCF-7	breast:
2	chr3:75867624..75868149-chr3:76093803..76094658,2	MCF-7	breast:
3	chr3:76077395..76079009-chr3:76080848..76082898,2	K562	blood:
4	chr3:76073881..76074768-chr3:76093884..76094767,3	MCF-7	breast:
5	chr3:76077395..76079009-chr3:76080848..76082898,2	K562	blood:

Variant related genes	Relation type
ENSG00000222883	TF binding region
ENSG00000222883	CpG island

Extended variants
information (count: 2362 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2362 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532818235	chr3:76015577-76015578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs557851689	chr3:76017004-76017005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540473789	chr3:76017025-76017026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150126220	chr3:76017109-76017110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2324461	chr3:76017154-76017155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551328546	chr3:76017216-76017217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561563311	chr3:76017225-76017226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147795222	chr3:76017236-76017237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs578096706	chr3:76017251-76017252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190336104	chr3:76017254-76017255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563961139	chr3:76017387-76017388	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs551761538	chr3:76017388-76017389	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs566857444	chr3:76017442-76017443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141135883	chr3:76017455-76017456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113331495	chr3:76017467-76017468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567488932	chr3:76017544-76017545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186244715	chr3:76017554-76017555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556085083	chr3:76017591-76017592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574249813	chr3:76017592-76017593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34342604	chr3:76017599-76017600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146917928	chr3:76017621-76017622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200514148	chr3:76017752-76017753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190889413	chr3:76017779-76017780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138560526	chr3:76017800-76017801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553682104	chr3:76017801-76017802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572066914	chr3:76017834-76017835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182761230	chr3:76017842-76017843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560803339	chr3:76017851-76017852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574311121	chr3:76017852-76017853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71101871	chr3:76017944-76017945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs398106052	chr3:76017948-76017949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs656099	chr3:76017955-76017956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369362408	chr3:76017966-76017967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533622502	chr3:76017992-76017993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551824616	chr3:76018002-76018003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs367863330	chr3:76018077-76018078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202239064	chr3:76018088-76018089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560505700	chr3:76018104-76018105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114924419	chr3:76018165-76018166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187473924	chr3:76018272-76018273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191501560	chr3:76018292-76018293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375723276	chr3:76018317-76018318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201995584	chr3:76018343-76018344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182496714	chr3:76018344-76018345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7428039	chr3:76018352-76018353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571210745	chr3:76018375-76018376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141517934	chr3:76018396-76018397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528958394	chr3:76018445-76018446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572040140	chr3:76018458-76018459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550219429	chr3:76018480-76018481	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	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
Chronic lymphocytic leukemia	20421269	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:76017000-76017400	Enhancers	Fetal Brain Female	brain
2	chr3:76017400-76018400	Weak transcription	Fetal Brain Female	brain
3	chr3:76018400-76018600	Enhancers	Fetal Brain Female	brain
4	chr3:76032000-76033400	Enhancers	Fetal Brain Male	brain
5	chr3:76036400-76036800	Active TSS	Adipose Nuclei	Adipose
6	chr3:76041200-76042000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
7	chr3:76041800-76042200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
8	chr3:76043400-76044200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
9	chr3:76059400-76059800	Enhancers	Adipose Nuclei	Adipose
10	chr3:76059400-76060600	Enhancers	Fetal Heart	heart
11	chr3:76060400-76060800	Enhancers	Left Ventricle	heart
12	chr3:76063600-76064200	Enhancers	Fetal Brain Male	brain
13	chr3:76064200-76065800	Weak transcription	Fetal Brain Male	brain
14	chr3:76065000-76066400	Enhancers	Fetal Brain Female	brain
15	chr3:76065800-76066200	Enhancers	Fetal Brain Male	brain
16	chr3:76065800-76066400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr3:76066000-76066400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr3:76066200-76066600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr3:76066200-76066600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr3:76066400-76066600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:76069000-76072200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr3:76070000-76073600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr3:76070600-76071000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:76070800-76071200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr3:76073000-76075200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr3:76073600-76073800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr3:76073600-76075200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:76073800-76074400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr3:76073800-76075000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr3:76074400-76075000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr3:76074400-76075200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr3:76074600-76074800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr3:76074600-76075200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr3:76074600-76075800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr3:76074800-76076000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:76075000-76075200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr3:76075200-76078000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr3:76075200-76078000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr3:76075200-76088000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr3:76075800-76076200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr3:76076200-76078000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr3:76077000-76084400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:76078000-76078200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr3:76078000-76078200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr3:76082400-76082600	Enhancers	H1 Cell Line	embryonic stem cell
46	chr3:76082400-76082600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr3:76082400-76082600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr3:76082400-76083000	Enhancers	H9 Cell Line	embryonic stem cell
49	chr3:76082600-76083600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr3:76082600-76084000	Weak transcription	H1 Cell Line	embryonic stem cell

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