Variant report

Variant	nsv874349
Chromosome Location	chr2:77965325-78048214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:78043808-78043996	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:78018338-78018524	HepG2	liver:	n/a	chr2:78018470-78018483 chr2:78018453-78018464
3	CEBPB	chr2:77995692-77996037	HepG2	liver:	n/a	chr2:77995852-77995863
4	CEBPB	chr2:77995750-77995921	HepG2	liver:	n/a	chr2:77995852-77995863
5	CEBPB	chr2:78029044-78029185	HepG2	liver:	n/a	chr2:78029126-78029139 chr2:78029127-78029138
6	CHD2	chr2:77981206-77981340	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr2:78023640-78023790	BE2_C	brain:	n/a	n/a
8	CTCF	chr2:78033617-78033669	Lung_OC	lung:	n/a	n/a
9	CTCF	chr2:78035672-78035707	Pancreas_OC	pancreas:	n/a	n/a
10	CTCF	chr2:78007686-78007720	Lung_OC	lung:	n/a	n/a
11	CTCF	chr2:78046932-78046967	GM20000	blood:	n/a	n/a
12	CTCF	chr2:78023640-78023790	Caco-2	colon:	n/a	n/a
13	CTCF	chr2:77999629-77999640	GM10248	blood:	n/a	n/a
14	CTCF	chr2:77996242-77996290	GM19239	blood:	n/a	n/a
15	CTCF	chr2:78037650-78037693	GM10248	blood:	n/a	n/a
16	CTCF	chr2:78023560-78023710	BE2_C	brain:	n/a	n/a
17	CTCF	chr2:77996793-77996806	GM13976	blood:	n/a	n/a
18	E2F4	chr2:77992385-77992727	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr2:78024715-78025098	MCF10A-Er-Src	breast:	n/a	n/a
20	EP300	chr2:78016788-78017750	SK-N-SH	brain:	n/a	n/a
21	EP300	chr2:78027511-78027934	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr2:77973960-77974183	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr2:78027585-78027826	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr2:78017913-78017915	HepG2	liver:	n/a	n/a
25	EP300	chr2:78027202-78027929	SK-N-SH	brain:	n/a	n/a
26	EP300	chr2:77973914-77974265	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr2:77973860-77974387	HepG2	liver:	n/a	n/a
28	FOS	chr2:78034937-78035262	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr2:78035048-78035255	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr2:78034997-78035233	MCF10A-Er-Src	breast:	n/a	n/a
31	FOSL2	chr2:77973960-77974261	HepG2	liver:	n/a	n/a
32	FOXA1	chr2:78005800-78006091	HepG2	liver:	n/a	n/a
33	FOXA1	chr2:77981195-77981403	HepG2	liver:	n/a	n/a
34	FOXA1	chr2:77973890-77974198	HepG2	liver:	n/a	n/a
35	FOXA1	chr2:77981178-77981433	HepG2	liver:	n/a	n/a
36	FOXA1	chr2:77981184-77981422	HepG2	liver:	n/a	n/a
37	FOXA1	chr2:77981177-77981433	HepG2	liver:	n/a	n/a
38	FOXA1	chr2:77973855-77974283	HepG2	liver:	n/a	n/a
39	FOXA1	chr2:77973887-77974238	HepG2	liver:	n/a	n/a
40	FOXA1	chr2:77973907-77974369	HepG2	liver:	n/a	n/a
41	FOXA2	chr2:77980995-77981492	A549	lung:	n/a	n/a
42	FOXA2	chr2:77981219-77981525	A549	lung:	n/a	n/a
43	FOXA2	chr2:78005851-78006049	HepG2	liver:	n/a	n/a
44	FOXA2	chr2:77973872-77974468	HepG2	liver:	n/a	n/a
45	FOXA2	chr2:77981207-77981387	HepG2	liver:	n/a	n/a
46	FOXA2	chr2:77973958-77974288	HepG2	liver:	n/a	n/a
47	GATA2	chr2:77973916-77974288	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr2:78027554-78027828	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr2:77973948-77974317	MCF-7	breast:	n/a	n/a
50	GATA3	chr2:77973938-77974345	SH-SY5Y	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:77981162-77981212	SK-N-SH_RA	brain:	n/a
2	chr2:77981162-77981212	HEK293	kidney:	embryo
3	chr2:77981162-77981212	T-47D	breast:	n/a
4	chr2:77981162-77981212	GM12892	blood:	n/a
5	chr2:77981162-77981212	ovcar-3	ovarian:	n/a
6	chr2:77981162-77981212	HRE	kidney:	n/a
7	chr2:77981162-77981212	ProgFib	skin:	n/a
8	chr2:77981162-77981212	HepG2	liver:	n/a
9	chr2:77981162-77981212	HRCEpiC	kidney:	n/a
10	chr2:77981162-77981212	HRPEpiC	eye:	n/a
11	chr2:77981162-77981212	SAEC	small airway:	n/a
12	chr2:77981162-77981212	AG04449	skin:	fetal
13	chr2:77981162-77981212	BJ	skin:	n/a
14	chr2:77981162-77981212	Jurkat	blood:	n/a
15	chr2:77981162-77981212	Caco-2	colon:	n/a
16	chr2:77981162-77981212	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:77981162-77981212	AG04450	lung:	fetal
18	chr2:77981162-77981212	RPTEC	kidney:	n/a
19	chr2:77981162-77981212	PrEC	prostate:	n/a
20	chr2:77981162-77981212	HMEC	breast:	n/a
21	chr2:77981162-77981212	IMR90	lung:	fetal
22	chr2:77981162-77981212	GM12878	blood:	n/a
23	chr2:77981162-77981212	PANC-1	pancreas:	n/a
24	chr2:77981162-77981212	NT2-D1	testis:	n/a
25	chr2:77981162-77981212	A549	lung:	n/a
26	chr2:77981162-77981212	HL-60	blood:	n/a
27	chr2:77981162-77981212	Hepatocyte	liver:	n/a
28	chr2:77981162-77981212	BE2_C	brain:	n/a
29	chr2:77981162-77981212	AoSMC	blood vessel:	n/a
30	chr2:77981162-77981212	U87	brain:	n/a
31	chr2:77981162-77981212	NHDF-neo	bronchial:	n/a
32	chr2:77981162-77981212	H1-hESC	embryonic stem cell:	embryo
33	chr2:77981162-77981212	SK-N-MC	brain:	n/a
34	chr2:77981162-77981212	ECC-1	luminal epithelium:	n/a
35	chr2:77981162-77981212	GM12891	blood:	n/a
36	chr2:77981162-77981212	HIPEpiC	eye:	n/a
37	chr2:77981162-77981212	CMK	blood:	n/a
38	chr2:77981162-77981212	HEEpiC	esophagus:	n/a
39	chr2:77981162-77981212	NH-A	brain:	n/a
40	chr2:77981162-77981212	HNPCEpiC	eye:	n/a
41	chr2:77981162-77981212	Hela-S3	cervix:	n/a
42	chr2:77981162-77981212	HCF	heart:	n/a
43	chr2:77981162-77981212	K562	blood:	n/a
44	chr2:77981162-77981212	HCPEpiC	choroid plexus:	n/a
45	chr2:77981162-77981212	HUVEC	blood vessel:	n/a
46	chr2:77981162-77981212	HCT-116	colon:	n/a
47	chr2:77981162-77981212	HAEpiC	amniotic membrane:	n/a
48	chr2:77981162-77981212	SKMC	muscle:	n/a
49	chr2:77981162-77981212	PFSK-1	brain:	n/a
50	chr2:77981162-77981212	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:56735169..56737848-chr2:78047828..78049670,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REG3G-10	chr2:77998337-77998625	l_1869_chr2:77996540-77998625_testes
2	lnc-REG3G-10	chr2:77996568-77996727	NONHSAT071832
3	lnc-REG3G-10	chr2:77997871-77998038	NONHSAT071832
4	lnc-REG3G-9	chr2:78015508-78015637	NONHSAT071833
5	lnc-REG3G-9	chr2:78013230-78013238	NONHSAT071833
6	lnc-REG3G-9	chr2:78014667-78014729	NONHSAT071833
7	lnc-REG3G-10	chr2:77996541-77996727	l_1869_chr2:77996540-77998625_testes
8	lnc-REG3G-10	chr2:77997871-77998038	l_1869_chr2:77996540-77998625_testes
9	lnc-REG3G-9	chr2:78019858-78020279	NONHSAT071833
10	lnc-REG3G-9	chr2:78019947-78020151	NONHSAT071834
11	lnc-LRRTM4-3	chr2:77970822-77970948	NR_110288
12	lnc-REG3G-10	chr2:77998337-77998643	NONHSAT071832

No data

Variant related genes	Relation type
ENSG00000237077	TF binding region
ENSG00000237077	CpG island
ENSG00000202077	chromatin interactions

Extended variants
information (count: 1849 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1849 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561061358	chr2:77970846-77970847	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs75292277	chr2:77970847-77970848	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs538200194	chr2:77970868-77970869	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs13395200	chr2:77970879-77970880	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs572147665	chr2:77970889-77970890	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs77125778	chr2:77970890-77970891	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs182043978	chr2:77970906-77970907	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs193204102	chr2:77974004-77974005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368576416	chr2:77974008-77974009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185196792	chr2:77974063-77974064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566567452	chr2:77974077-77974078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113805534	chr2:77974089-77974090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549012616	chr2:77974090-77974091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568774143	chr2:77974151-77974152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs3021417	chr2:77974218-77974219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537736857	chr2:77974222-77974223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564932236	chr2:77974245-77974246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112866288	chr2:77974250-77974251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2954560	chr2:77974317-77974318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs56141785	chr2:77974321-77974322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs397936378	chr2:77974327-77974328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77595223	chr2:77974328-77974329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2931478	chr2:77974346-77974347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535671051	chr2:77974433-77974434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34995983	chr2:77974451-77974452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368126521	chr2:77974460-77974461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs116267384	chr2:77974465-77974466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1825757	chr2:77974500-77974501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4103633	chr2:77974507-77974508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4103634	chr2:77974514-77974515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554203063	chr2:77974518-77974519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147217638	chr2:77974559-77974560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536806001	chr2:77974561-77974562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371971016	chr2:77974592-77974593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190488676	chr2:77974597-77974598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs56006143	chr2:77974605-77974606	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs10206651	chr2:77974612-77974613	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs2931479	chr2:77974647-77974648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs193119185	chr2:77974662-77974663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561007862	chr2:77974663-77974664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116252546	chr2:77974672-77974673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557574769	chr2:77974686-77974687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528192926	chr2:77974694-77974695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2931480	chr2:77974720-77974721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139583191	chr2:77974729-77974730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575209781	chr2:77974736-77974737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149714432	chr2:77974762-77974763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529089934	chr2:77974765-77974766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548808808	chr2:77974777-77974778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79342935	chr2:77974802-77974803	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:77974000-77975200	Enhancers	HepG2	liver
2	chr2:77975000-77975200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:77975200-77975600	Weak transcription	HepG2	liver
4	chr2:77975200-77980800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:77975600-77976000	Enhancers	HepG2	liver
6	chr2:77977200-77977600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:77979400-77980000	Enhancers	H9 Cell Line	embryonic stem cell
8	chr2:77980000-77980800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr2:77980400-77980600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr2:77980600-77980800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr2:77980600-77981400	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr2:77980600-77981400	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr2:77980600-77981400	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr2:77980600-77981400	Active TSS	iPS-18 Cell Line	embryonic stem cell
15	chr2:77980600-77981400	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr2:77980600-77981600	Active TSS	H1 Cell Line	embryonic stem cell
17	chr2:77980600-77981600	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr2:77980800-77981200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr2:77980800-77981400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr2:77980800-77981400	Active TSS	H9 Cell Line	embryonic stem cell
21	chr2:77980800-77981400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:77980800-77981400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr2:77980800-77981600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:77980800-77981600	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr2:77980800-77981600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:77994400-77994800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:77994600-77995000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr2:77994600-77996200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:77995000-77995200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:77995000-77997400	Weak transcription	Right Atrium	heart
31	chr2:77995200-77996200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr2:77996200-77996400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:77996200-77996400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:77996400-77999800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr2:77999800-78000400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr2:78013600-78014200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:78013800-78014600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr2:78014000-78014400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:78017800-78018000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:78018000-78021200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:78023800-78024600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr2:78023800-78025000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr2:78023800-78025200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:78024200-78024600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:78024200-78024800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr2:78024400-78025200	Enhancers	H9 Cell Line	embryonic stem cell
47	chr2:78031000-78031200	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr2:78031400-78032000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr2:78031600-78031800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr2:78031800-78033000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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