Variant report

Variant	esv1795979
Chromosome Location	chr2:79075753-79226086
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	chr2:79194367-79194855	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:79206796-79207089	HepG2	liver:	n/a	n/a
3	ATF2	chr2:79204595-79205184	GM12878	blood:	n/a	n/a
4	ATF2	chr2:79204610-79205233	GM12878	blood:	n/a	n/a
5	BACH1	chr2:79080206-79080246	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:79194565-79194567	K562	blood:	n/a	n/a
7	BACH1	chr2:79220061-79220237	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:79080125-79080365	K562	blood:	n/a	n/a
9	BACH1	chr2:79144694-79144730	K562	blood:	n/a	n/a
10	BATF	chr2:79204698-79205289	GM12878	blood:	n/a	n/a
11	BATF	chr2:79156569-79156744	GM12878	blood:	n/a	n/a
12	BATF	chr2:79122109-79122342	GM12878	blood:	n/a	chr2:79122236-79122246 chr2:79122239-79122250
13	BATF	chr2:79204689-79205086	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:79204752-79205084	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:79204611-79205350	GM12878	blood:	n/a	n/a
16	BCL3	chr2:79204672-79204956	GM12878	blood:	n/a	n/a
17	BCLAF1	chr2:79204679-79205230	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:79208050-79208362	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:79204500-79205297	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:79194402-79194761	HepG2	liver:	n/a	n/a
21	BRCA1	chr2:79206931-79206936	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:79084624-79084894	HepG2	liver:	n/a	chr2:79084732-79084749 chr2:79084735-79084746
23	CEBPB	chr2:79194363-79194806	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:79102798-79103102	K562	blood:	n/a	n/a
25	CEBPB	chr2:79154553-79154899	HepG2	liver:	n/a	chr2:79154726-79154735 chr2:79154725-79154736 chr2:79154726-79154735 chr2:79154726-79154735 chr2:79154726-79154735
26	CEBPB	chr2:79132157-79132397	A549	lung:	n/a	chr2:79132267-79132278 chr2:79132268-79132279 chr2:79132267-79132280 chr2:79132267-79132280 chr2:79132267-79132280
27	CEBPB	chr2:79089932-79090155	H1-hESC	embryonic stem cell:	n/a	chr2:79090053-79090062 chr2:79090052-79090063
28	CEBPB	chr2:79128808-79129127	HepG2	liver:	n/a	chr2:79128947-79128958
29	CEBPB	chr2:79132102-79132405	IMR90	lung:	n/a	chr2:79132267-79132278 chr2:79132268-79132279 chr2:79132267-79132280 chr2:79132267-79132280 chr2:79132267-79132280
30	CEBPB	chr2:79136191-79136412	H1-hESC	embryonic stem cell:	n/a	chr2:79136320-79136328 chr2:79136306-79136317
31	CEBPB	chr2:79154601-79154854	K562	blood:	n/a	chr2:79154726-79154735 chr2:79154725-79154736 chr2:79154726-79154735 chr2:79154726-79154735 chr2:79154726-79154735
32	CEBPB	chr2:79154569-79154870	IMR90	lung:	n/a	chr2:79154726-79154735 chr2:79154725-79154736 chr2:79154726-79154735 chr2:79154726-79154735 chr2:79154726-79154735
33	CEBPB	chr2:79084620-79084829	IMR90	lung:	n/a	chr2:79084732-79084749 chr2:79084735-79084746
34	CEBPB	chr2:79176907-79177257	HepG2	liver:	n/a	chr2:79177075-79177086 chr2:79177076-79177085
35	CEBPB	chr2:79136127-79136491	HepG2	liver:	n/a	chr2:79136320-79136328 chr2:79136306-79136317
36	CEBPB	chr2:79226012-79226201	K562	blood:	n/a	chr2:79226065-79226076
37	CEBPB	chr2:79226078-79226081	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:79083857-79084434	Hela-S3	cervix:	n/a	chr2:79084246-79084259 chr2:79084248-79084259 chr2:79084248-79084259
39	CEBPB	chr2:79089900-79090207	HepG2	liver:	n/a	chr2:79090053-79090062 chr2:79090052-79090063
40	CEBPB	chr2:79225919-79226205	HepG2	liver:	n/a	chr2:79226065-79226076
41	CEBPB	chr2:79136147-79136482	HepG2	liver:	n/a	chr2:79136320-79136328 chr2:79136306-79136317
42	CEBPB	chr2:79225944-79226227	IMR90	lung:	n/a	chr2:79226065-79226076
43	CEBPB	chr2:79154556-79154826	A549	lung:	n/a	chr2:79154726-79154735 chr2:79154725-79154736 chr2:79154726-79154735 chr2:79154726-79154735 chr2:79154726-79154735
44	CEBPB	chr2:79084624-79084869	A549	lung:	n/a	chr2:79084732-79084749 chr2:79084735-79084746
45	CEBPB	chr2:79136153-79136460	Hela-S3	cervix:	n/a	chr2:79136320-79136328 chr2:79136306-79136317
46	CEBPB	chr2:79092549-79092844	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr2:79220950-79221075	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr2:79096056-79096281	K562	blood:	n/a	chr2:79096183-79096194 chr2:79096185-79096196 chr2:79096183-79096196 chr2:79096183-79096196 chr2:79096185-79096196
49	CEBPB	chr2:79132096-79132426	HepG2	liver:	n/a	chr2:79132267-79132278 chr2:79132268-79132279 chr2:79132267-79132280 chr2:79132267-79132280 chr2:79132267-79132280
50	CEBPB	chr2:79096032-79096336	HepG2	liver:	n/a	chr2:79096183-79096194 chr2:79096185-79096196 chr2:79096183-79096196 chr2:79096183-79096196 chr2:79096185-79096196

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:79220528-79220578	GM12891	blood:	n/a
2	chr2:79220528-79220578	LNCaP	prostate:	n/a
3	chr2:79216742-79216792	HPAEpiC	pulmonary alveolar:	n/a
4	chr2:79220510-79220560	HNPCEpiC	eye:	n/a
5	chr2:79220510-79220560	NHBE	bronchial:	n/a
6	chr2:79216742-79216792	IMR90	lung:	fetal
7	chr2:79220528-79220578	MCF10A-Er-Src	breast:	n/a
8	chr2:79218384-79218434	SK-N-SH	brain:	n/a
9	chr2:79221130-79221180	Caco-2	colon:	n/a
10	chr2:79223172-79223222	H1-hESC	embryonic stem cell:	embryo
11	chr2:79216742-79216792	HIPEpiC	eye:	n/a
12	chr2:79216742-79216792	SAEC	small airway:	n/a
13	chr2:79223172-79223222	HEK293	kidney:	embryo
14	chr2:79221130-79221180	AG09319	gingival:	n/a
15	chr2:79220381-79220431	ProgFib	skin:	n/a
16	chr2:79220217-79220267	PrEC	prostate:	n/a
17	chr2:79220528-79220578	GM19239	blood:	n/a
18	chr2:79220510-79220560	HCPEpiC	choroid plexus:	n/a
19	chr2:79220029-79220079	CMK	blood:	n/a
20	chr2:79220217-79220267	HEEpiC	esophagus:	n/a
21	chr2:79220528-79220578	HCPEpiC	choroid plexus:	n/a
22	chr2:79223172-79223222	HL-60	blood:	n/a
23	chr2:79220029-79220079	BE2_C	brain:	n/a
24	chr2:79220381-79220431	GM12891	blood:	n/a
25	chr2:79223172-79223222	AG09319	gingival:	n/a
26	chr2:79221130-79221180	HRCEpiC	kidney:	n/a
27	chr2:79223172-79223222	GM12891	blood:	n/a
28	chr2:79220381-79220431	T-47D	breast:	n/a
29	chr2:79218384-79218434	BJ	skin:	n/a
30	chr2:79220217-79220267	IMR90	lung:	fetal
31	chr2:79220510-79220560	GM06990	blood:	n/a
32	chr2:79220881-79220931	GM06990	blood:	n/a
33	chr2:79223172-79223222	HRCEpiC	kidney:	n/a
34	chr2:79220381-79220431	HepG2	liver:	n/a
35	chr2:79220510-79220560	NB4	blood:	n/a
36	chr2:79220217-79220267	RPTEC	kidney:	n/a
37	chr2:79220217-79220267	HepG2	liver:	n/a
38	chr2:79220029-79220079	A549	lung:	n/a
39	chr2:79221130-79221180	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:79223172-79223222	HIPEpiC	eye:	n/a
41	chr2:79216742-79216792	HCPEpiC	choroid plexus:	n/a
42	chr2:79218384-79218434	HIPEpiC	eye:	n/a
43	chr2:79221130-79221180	Jurkat	blood:	n/a
44	chr2:79220528-79220578	Jurkat	blood:	n/a
45	chr2:79220881-79220931	SK-N-SH	brain:	n/a
46	chr2:79220881-79220931	HEK293	kidney:	embryo
47	chr2:79218384-79218434	NT2-D1	testis:	n/a
48	chr2:79216742-79216792	AG09319	gingival:	n/a
49	chr2:79218384-79218434	LNCaP	prostate:	n/a
50	chr2:79220381-79220431	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:78577613..78578539-chr2:79206466..79207847,3	MCF-7	breast:
2	chr2:79084347..79087300-chr2:79103800..79106466,2	K562	blood:
3	chr2:79084347..79087300-chr2:79103800..79106466,2	K562	blood:
4	chr2:78899834..78900793-chr2:79088429..79089440,4	MCF-7	breast:
5	chr2:78658362..78658925-chr2:79089675..79090181,2	MCF-7	breast:
6	chr2:79219262..79219850-chr2:79446247..79447295,3	MCF-7	breast:
7	chr2:79219232..79220225-chr2:80087317..80087950,2	MCF-7	breast:
8	chr2:79151621..79153755-chr2:79157676..79159858,2	K562	blood:
9	chr2:78898994..78900712-chr2:79206429..79207134,5	MCF-7	breast:
10	chr2:78658404..78659062-chr2:79206498..79207224,3	MCF-7	breast:
11	chr2:79106389..79108042-chr2:79109132..79111670,2	MCF-7	breast:
12	chr2:78578299..78578916-chr2:79206809..79207351,2	MCF-7	breast:
13	chr2:79151621..79153755-chr2:79157676..79159858,2	K562	blood:
14	chr2:79136865..79138621-chr2:79143164..79145984,2	K562	blood:
15	chr2:79136865..79138621-chr2:79143164..79145984,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG1B-2	chr2:79108611-79108749	XLOC_002177
2	lnc-REG1B-1	chr2:79157903-79158506	XLOC_002178
3	lnc-REG1B-2	chr2:79107908-79108018	XLOC_002177
4	lnc-REG1B-3	chr2:79102285-79102649	XLOC_002176
5	lnc-REG1B-3	chr2:79107618-79107703	XLOC_002176
6	lnc-REG1B-1	chr2:79146572-79146651	XLOC_002178

Variant related genes	Relation type
RNU6-812P	TF binding region
RNU6-827P	TF binding region
RNU6-812P	CpG island
RNU6-827P	CpG island
ENSG00000200048	chromatin interactions
ENSG00000202423	chromatin interactions

Extended variants
information (count: 2535 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2535 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142236679	chr2:79082829-79082830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188227007	chr2:79082839-79082840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560671223	chr2:79082854-79082855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192970770	chr2:79082951-79082952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542423520	chr2:79083040-79083041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550353484	chr2:79083058-79083059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185194394	chr2:79083084-79083085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532832882	chr2:79083121-79083122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146403658	chr2:79083181-79083182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112227210	chr2:79083208-79083209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557400977	chr2:79083277-79083278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566058903	chr2:79083282-79083283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535042067	chr2:79083286-79083287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1521965	chr2:79083305-79083306	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568547754	chr2:79083422-79083423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139484826	chr2:79083426-79083427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556318991	chr2:79083452-79083453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576195934	chr2:79083458-79083459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536491245	chr2:79083464-79083465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540141227	chr2:79083471-79083472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533331674	chr2:79083472-79083473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369642874	chr2:79083480-79083481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6707481	chr2:79083525-79083526	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs369246826	chr2:79083616-79083617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558451834	chr2:79083639-79083640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6707613	chr2:79083666-79083667	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs540641354	chr2:79083725-79083726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188956850	chr2:79083753-79083754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574473076	chr2:79083756-79083757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558396113	chr2:79084213-79084214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17015740	chr2:79084215-79084216	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs534647072	chr2:79084220-79084221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112215578	chr2:79084262-79084263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188290350	chr2:79084335-79084336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs180870815	chr2:79084341-79084342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574384099	chr2:79084442-79084443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs28612822	chr2:79084488-79084489	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs563262193	chr2:79084501-79084502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577336136	chr2:79084603-79084604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561148095	chr2:79084604-79084605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546431715	chr2:79084640-79084641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372537647	chr2:79084645-79084646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560038645	chr2:79084650-79084651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528789699	chr2:79084653-79084654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139778414	chr2:79084680-79084681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561123224	chr2:79084724-79084725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186505343	chr2:79084726-79084727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189771268	chr2:79084768-79084769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528264308	chr2:79084781-79084782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547128247	chr2:79084920-79084921	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Intracranial tumor	22048656	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:79082800-79083800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:79084200-79085000	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr2:79084600-79085400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr2:79084800-79085400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr2:79085000-79085400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:79085000-79085400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr2:79085400-79086000	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr2:79086000-79088800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr2:79089800-79090200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr2:79096200-79097800	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr2:79096600-79100800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:79097400-79097800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr2:79097400-79098600	Enhancers	Primary B cells from cord blood	blood
14	chr2:79097400-79098800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr2:79097800-79098200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr2:79097800-79098200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr2:79098200-79098600	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr2:79098200-79099400	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr2:79098600-79098800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr2:79098800-79100000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr2:79105400-79106800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:79106600-79107400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr2:79110800-79111200	Enhancers	HUVEC	blood vessel
24	chr2:79114400-79115200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr2:79116000-79116400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr2:79116200-79116600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:79127200-79127600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:79127200-79127600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:79133400-79133600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:79133400-79133800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:79133800-79137400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:79136000-79136400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr2:79136400-79140200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr2:79137400-79138200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr2:79138200-79143400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr2:79139200-79141200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr2:79139200-79141200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:79139400-79140800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:79139400-79141400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr2:79139600-79140600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:79140000-79141000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr2:79140200-79140600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr2:79140200-79140800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr2:79140200-79140800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:79140200-79141000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr2:79143200-79143400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:79152800-79153000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:79152800-79153000	Enhancers	Fetal Kidney	kidney
49	chr2:79155600-79156000	Active TSS	Monocytes-CD14+_RO01746	blood
50	chr2:79163600-79163800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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