Variant report

Variant	nsv902116
Chromosome Location	chr14:81018237-81082400
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	chr14:81043880-81044402	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:81053313-81053670	HepG2	liver:	n/a	n/a
3	ATF2	chr14:81053358-81054228	GM12878	blood:	n/a	n/a
4	ATF2	chr14:81027150-81027546	GM12878	blood:	n/a	n/a
5	ATF2	chr14:81053401-81054105	GM12878	blood:	n/a	n/a
6	BATF	chr14:81027117-81027551	GM12878	blood:	n/a	chr14:81027325-81027335 chr14:81027320-81027331
7	BATF	chr14:81053406-81054170	GM12878	blood:	n/a	chr14:81054156-81054164
8	BATF	chr14:81027222-81027425	GM12878	blood:	n/a	chr14:81027325-81027335 chr14:81027320-81027331
9	BATF	chr14:81042164-81042474	GM12878	blood:	n/a	chr14:81042258-81042268
10	BATF	chr14:81053502-81054107	GM12878	blood:	n/a	n/a
11	BCL11A	chr14:81053456-81054128	GM12878	blood:	n/a	n/a
12	BCL11A	chr14:81053563-81054024	GM12878	blood:	n/a	n/a
13	BCL3	chr14:81053494-81053956	GM12878	blood:	n/a	n/a
14	BCL3	chr14:81053669-81054077	GM12878	blood:	n/a	n/a
15	BCLAF1	chr14:81053454-81053999	GM12878	blood:	n/a	n/a
16	BCLAF1	chr14:81053348-81054147	GM12878	blood:	n/a	n/a
17	BHLHE40	chr14:81053453-81054112	GM12878	blood:	n/a	n/a
18	CEBPB	chr14:81025166-81025438	IMR90	lung:	n/a	chr14:81025308-81025319 chr14:81025309-81025320
19	CEBPB	chr14:81051579-81051944	HCT-116	colon:	n/a	n/a
20	CEBPB	chr14:81070707-81070941	HepG2	liver:	n/a	chr14:81070849-81070860
21	CEBPB	chr14:81031329-81031869	MCF-7	breast:	n/a	n/a
22	CEBPB	chr14:81070720-81071002	IMR90	lung:	n/a	chr14:81070849-81070860
23	CEBPB	chr14:81053705-81054013	GM12878	blood:	n/a	chr14:81053777-81053789
24	CEBPB	chr14:81031342-81031715	MCF-7	breast:	n/a	n/a
25	CEBPB	chr14:81025191-81025417	A549	lung:	n/a	chr14:81025308-81025319 chr14:81025309-81025320
26	CEBPB	chr14:81053359-81054257	GM12878	blood:	n/a	chr14:81053615-81053627 chr14:81053777-81053789
27	CEBPB	chr14:81051562-81051982	HCT-116	colon:	n/a	n/a
28	CEBPB	chr14:81036091-81036241	HepG2	liver:	n/a	chr14:81036144-81036155
29	CEBPB	chr14:81025244-81025415	HepG2	liver:	n/a	chr14:81025308-81025319 chr14:81025309-81025320
30	CEBPB	chr14:81051335-81052078	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:81075588-81075623	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr14:81053584-81054012	GM12878	blood:	n/a	n/a
33	CREB1	chr14:81053468-81054161	GM12878	blood:	n/a	n/a
34	CREB1	chr14:81053479-81054172	GM12878	blood:	n/a	n/a
35	CTCF	chr14:81053462-81053678	Spleen_OC	spleen:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
36	CTCF	chr14:81053480-81053630	Hela-S3	cervix:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
37	CTCF	chr14:81052500-81052650	HCT-116	colon:	n/a	n/a
38	CTCF	chr14:81053381-81053768	IMR90	lung:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
39	CTCF	chr14:81053440-81053590	HRPEpiC	eye:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
40	CTCF	chr14:81053460-81053610	GM12878	blood:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
41	CTCF	chr14:81053480-81053630	AG10803	skin:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
42	CTCF	chr14:81053480-81053630	Caco-2	colon:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
43	CTCF	chr14:81053540-81053690	HL-60	blood:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
44	CTCF	chr14:81053476-81053654	A549	lung:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
45	CTCF	chr14:81053600-81053750	A549	lung:	n/a	n/a
46	CTCF	chr14:81053420-81053570	GM12872	blood:	n/a	chr14:81053549-81053570
47	CTCF	chr14:81039180-81039330	HCT-116	colon:	n/a	chr14:81039211-81039229 chr14:81039217-81039226
48	CTCF	chr14:81053400-81053550	HFF	foreskin:	n/a	n/a
49	CTCF	chr14:81053480-81053630	GM12873	blood:	n/a	chr14:81053549-81053570 chr14:81053554-81053572
50	CTCF	chr14:81053480-81053630	HA-sp	spinal cord:	n/a	chr14:81053549-81053570 chr14:81053554-81053572

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81032132-81032182	NHBE	bronchial:	n/a
2	chr14:81032132-81032182	AG04450	lung:	fetal
3	chr14:81032132-81032182	HCPEpiC	choroid plexus:	n/a
4	chr14:81032132-81032182	SK-N-SH	brain:	n/a
5	chr14:81035143-81035193	HUVEC	blood vessel:	n/a
6	chr14:81032132-81032182	HRPEpiC	eye:	n/a
7	chr14:81035143-81035193	AG10803	skin:	n/a
8	chr14:81075111-81075161	NHDF-neo	bronchial:	n/a
9	chr14:81032132-81032182	U87	brain:	n/a
10	chr14:81032132-81032182	Hepatocyte	liver:	n/a
11	chr14:81032132-81032182	MCF-7	breast:	n/a
12	chr14:81075111-81075161	A549	lung:	n/a
13	chr14:81035143-81035193	HRE	kidney:	n/a
14	chr14:81075111-81075161	SK-N-SH	brain:	n/a
15	chr14:81032132-81032182	Jurkat	blood:	n/a
16	chr14:81075111-81075161	HNPCEpiC	eye:	n/a
17	chr14:81075111-81075161	ovcar-3	ovarian:	n/a
18	chr14:81032132-81032182	T-47D	breast:	n/a
19	chr14:81035143-81035193	GM12878	blood:	n/a
20	chr14:81035143-81035193	PrEC	prostate:	n/a
21	chr14:81035143-81035193	HCPEpiC	choroid plexus:	n/a
22	chr14:81032132-81032182	NB4	blood:	n/a
23	chr14:81075111-81075161	NHBE	bronchial:	n/a
24	chr14:81032132-81032182	GM12892	blood:	n/a
25	chr14:81035143-81035193	Jurkat	blood:	n/a
26	chr14:81032132-81032182	AG04449	skin:	fetal
27	chr14:81035143-81035193	HCM	heart:	n/a
28	chr14:81032132-81032182	PANC-1	pancreas:	n/a
29	chr14:81035143-81035193	SAEC	small airway:	n/a
30	chr14:81035143-81035193	ECC-1	luminal epithelium:	n/a
31	chr14:81075111-81075161	GM12891	blood:	n/a
32	chr14:81035143-81035193	GM12892	blood:	n/a
33	chr14:81035143-81035193	NHDF-neo	bronchial:	n/a
34	chr14:81075111-81075161	SK-N-MC	brain:	n/a
35	chr14:81032132-81032182	PFSK-1	brain:	n/a
36	chr14:81032132-81032182	HNPCEpiC	eye:	n/a
37	chr14:81032132-81032182	BE2_C	brain:	n/a
38	chr14:81035143-81035193	HepG2	liver:	n/a
39	chr14:81035143-81035193	T-47D	breast:	n/a
40	chr14:81035143-81035193	HNPCEpiC	eye:	n/a
41	chr14:81032132-81032182	ProgFib	skin:	n/a
42	chr14:81032132-81032182	HCF	heart:	n/a
43	chr14:81035143-81035193	Caco-2	colon:	n/a
44	chr14:81035143-81035193	NT2-D1	testis:	n/a
45	chr14:81032132-81032182	HIPEpiC	eye:	n/a
46	chr14:81035143-81035193	IMR90	lung:	fetal
47	chr14:81035143-81035193	HAEpiC	amniotic membrane:	n/a
48	chr14:81075111-81075161	HepG2	liver:	n/a
49	chr14:81035143-81035193	HCF	heart:	n/a
50	chr14:81032132-81032182	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:81033414..81035767-chr14:81040796..81044689,3	MCF-7	breast:
2	chr14:81075319..81077418-chr14:81079123..81081073,2	K562	blood:
3	chr14:80668488..80671365-chr14:81052766..81054886,2	MCF-7	breast:
4	chr14:81006375..81008300-chr14:81025497..81027246,2	MCF-7	breast:
5	chr14:81033414..81035767-chr14:81040796..81044689,3	MCF-7	breast:
6	chr14:81030392..81031930-chr14:81036761..81039029,2	MCF-7	breast:
7	chr14:81030392..81031930-chr14:81036761..81039029,2	MCF-7	breast:
8	chr14:81071464..81074082-chr14:81074931..81076557,2	MCF-7	breast:
9	chr14:81071464..81074082-chr14:81074931..81076557,2	MCF-7	breast:
10	chr14:80679969..80680577-chr14:81052998..81054035,4	MCF-7	breast:
11	chr14:81075319..81077418-chr14:81079123..81081073,2	K562	blood:

Variant related genes	Relation type
CEP128	TF binding region
CEP128	CpG island

Extended variants
information (count: 2355 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2355 , 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	rs10140845	chr14:81018237-81018238	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10140856	chr14:81018249-81018250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574494517	chr14:81018272-81018273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189486781	chr14:81018325-81018326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567186993	chr14:81018337-81018338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536705914	chr14:81018377-81018378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562350036	chr14:81018380-81018381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150734253	chr14:81018465-81018466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12434618	chr14:81018484-81018485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546117947	chr14:81018535-81018536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564720860	chr14:81018544-81018545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150047273	chr14:81018577-81018578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547321213	chr14:81018578-81018579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs8005242	chr14:81018606-81018607	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs529756407	chr14:81018607-81018608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61981671	chr14:81018619-81018620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs10717714	chr14:81018654-81018655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569677607	chr14:81018665-81018666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191422208	chr14:81018722-81018723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574903031	chr14:81018748-81018749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558432625	chr14:81018751-81018752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570644864	chr14:81018863-81018864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368883778	chr14:81018902-81018903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534556570	chr14:81018953-81018954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552855128	chr14:81018989-81018990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574480635	chr14:81019003-81019004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373199906	chr14:81019073-81019074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557413579	chr14:81019080-81019081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146114568	chr14:81019116-81019117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546303764	chr14:81019201-81019202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140198482	chr14:81019211-81019212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376465301	chr14:81019282-81019283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12435450	chr14:81019300-81019301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559233759	chr14:81019306-81019307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372586427	chr14:81019307-81019308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573486789	chr14:81019323-81019324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540920429	chr14:81019360-81019361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562414534	chr14:81019381-81019382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143875148	chr14:81019385-81019386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548241578	chr14:81019404-81019405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369863240	chr14:81019423-81019424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112403874	chr14:81019427-81019428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34517728	chr14:81019428-81019429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530492486	chr14:81019431-81019432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552249966	chr14:81019435-81019436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146788779	chr14:81019471-81019472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111514726	chr14:81019499-81019500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546469908	chr14:81019555-81019556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140471019	chr14:81019595-81019596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183933174	chr14:81019600-81019601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81013200-81023800	Weak transcription	Dnd41	blood
2	chr14:81020600-81021800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:81021800-81025400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:81023800-81024800	Strong transcription	Dnd41	blood
5	chr14:81024800-81029400	Weak transcription	Dnd41	blood
6	chr14:81025400-81026600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:81028400-81033400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:81029400-81029600	ZNF genes & repeats	Dnd41	blood
9	chr14:81029600-81044800	Weak transcription	Dnd41	blood
10	chr14:81030600-81031400	Enhancers	Placenta Amnion	Placenta Amnion
11	chr14:81031000-81032000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:81031000-81032000	Enhancers	Placenta	Placenta
13	chr14:81031400-81031800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr14:81031400-81032000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr14:81031400-81032000	Enhancers	H9 Cell Line	embryonic stem cell
16	chr14:81031400-81032200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr14:81031400-81032400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:81031600-81032000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr14:81031600-81032400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr14:81031600-81032600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr14:81031800-81032000	Enhancers	Placenta Amnion	Placenta Amnion
22	chr14:81031800-81032400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr14:81032000-81033400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr14:81032000-81034000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr14:81032200-81034400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr14:81032400-81040400	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr14:81033000-81034200	Enhancers	NHEK	skin
28	chr14:81033200-81034200	Enhancers	HMEC	breast
29	chr14:81033400-81034000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr14:81033400-81034200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:81033400-81034400	Enhancers	Placenta Amnion	Placenta Amnion
32	chr14:81033400-81035600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr14:81034000-81034600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr14:81034000-81034800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr14:81034000-81034800	Enhancers	Hela-S3	cervix
36	chr14:81034000-81035000	Enhancers	NH-A	brain
37	chr14:81034000-81035600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr14:81034200-81034400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr14:81034200-81034400	Enhancers	A549	lung
40	chr14:81034200-81034800	Flanking Active TSS	NHEK	skin
41	chr14:81034200-81035000	Flanking Active TSS	HMEC	breast
42	chr14:81034400-81034800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:81034400-81034800	Flanking Active TSS	A549	lung
44	chr14:81034400-81034800	Enhancers	HSMM	muscle
45	chr14:81034400-81034800	Enhancers	NHLF	lung
46	chr14:81034400-81034800	Enhancers	Osteobl	bone
47	chr14:81034400-81035000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr14:81034400-81035200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr14:81034600-81034800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:81034800-81035000	Enhancers	A549	lung

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