Variant report

Variant	esv2761012
Chromosome Location	chr6:87349163-87475193
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:87392792-87393956	K562	blood:	n/a	n/a
2	ARID3A	chr6:87394843-87395342	K562	blood:	n/a	n/a
3	ATF1	chr6:87394954-87395205	K562	blood:	n/a	n/a
4	ATF1	chr6:87410117-87410320	K562	blood:	n/a	n/a
5	ATF1	chr6:87392891-87393627	K562	blood:	n/a	n/a
6	BCL11A	chr6:87466373-87466627	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr6:87392836-87393518	K562	blood:	n/a	n/a
8	BHLHE40	chr6:87394959-87395310	K562	blood:	n/a	n/a
9	BRCA1	chr6:87368528-87368609	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr6:87392934-87393686	K562	blood:	n/a	n/a
11	CBX3	chr6:87469730-87470014	K562	blood:	n/a	n/a
12	CBX3	chr6:87382079-87382469	K562	blood:	n/a	n/a
13	CBX3	chr6:87392924-87393577	K562	blood:	n/a	n/a
14	CBX3	chr6:87382089-87382437	K562	blood:	n/a	n/a
15	CCNT2	chr6:87392719-87393684	K562	blood:	n/a	n/a
16	CCNT2	chr6:87462269-87462510	K562	blood:	n/a	n/a
17	CEBPB	chr6:87425303-87425740	MCF-7	breast:	n/a	n/a
18	CEBPB	chr6:87419910-87420164	IMR90	lung:	n/a	chr6:87420024-87420035
19	CEBPB	chr6:87425384-87425742	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr6:87392704-87393593	K562	blood:	n/a	n/a
21	CEBPB	chr6:87425344-87425752	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr6:87433225-87433948	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr6:87425232-87425884	MCF-7	breast:	n/a	n/a
24	CEBPB	chr6:87392678-87393131	K562	blood:	n/a	n/a
25	CEBPB	chr6:87419952-87420156	K562	blood:	n/a	chr6:87420024-87420035
26	CEBPB	chr6:87433390-87433855	MCF-7	breast:	n/a	n/a
27	CEBPB	chr6:87431910-87432114	A549	lung:	n/a	n/a
28	CEBPB	chr6:87419909-87420217	HepG2	liver:	n/a	chr6:87420024-87420035
29	CEBPB	chr6:87456318-87456518	H1-hESC	embryonic stem cell:	n/a	chr6:87456436-87456447
30	CEBPB	chr6:87425432-87425675	A549	lung:	n/a	n/a
31	CEBPB	chr6:87425420-87425682	K562	blood:	n/a	n/a
32	CEBPB	chr6:87456275-87456563	HepG2	liver:	n/a	chr6:87456436-87456447
33	CEBPB	chr6:87393184-87393650	K562	blood:	n/a	n/a
34	CEBPB	chr6:87425374-87425678	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr6:87433402-87433967	MCF-7	breast:	n/a	n/a
36	CEBPB	chr6:87435249-87435410	K562	blood:	n/a	n/a
37	CEBPB	chr6:87425358-87425752	Hela-S3	cervix:	n/a	n/a
38	CEBPD	chr6:87392754-87393740	K562	blood:	n/a	n/a
39	CEBPD	chr6:87394883-87395359	K562	blood:	n/a	n/a
40	CEBPD	chr6:87392874-87393747	K562	blood:	n/a	n/a
41	CEBPD	chr6:87394871-87395367	K562	blood:	n/a	n/a
42	CREB1	chr6:87466320-87466767	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr6:87392841-87393742	K562	blood:	n/a	n/a
44	CTCF	chr6:87416258-87416477	GM12891	blood:	n/a	n/a
45	CTCF	chr6:87416300-87416450	GM12865	blood:	n/a	n/a
46	CTCF	chr6:87416260-87416410	GM12865	blood:	n/a	n/a
47	CTCF	chr6:87416155-87416603	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:87416240-87416390	GM12870	blood:	n/a	n/a
49	CTCF	chr6:87416300-87416450	HL-60	blood:	n/a	n/a
50	CTCF	chr6:87416100-87416250	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:87380671-87380721	HCM	heart:	n/a
2	chr6:87466574-87466624	HepG2	liver:	n/a
3	chr6:87380615-87380665	GM06990	blood:	n/a
4	chr6:87380671-87380721	GM06990	blood:	n/a
5	chr6:87380615-87380665	NHDF-neo	bronchial:	n/a
6	chr6:87466574-87466624	HCPEpiC	choroid plexus:	n/a
7	chr6:87380615-87380665	AG09319	gingival:	n/a
8	chr6:87380671-87380721	IMR90	lung:	fetal
9	chr6:87380671-87380721	HCT-116	colon:	n/a
10	chr6:87380615-87380665	AG10803	skin:	n/a
11	chr6:87380615-87380665	HEK293	kidney:	embryo
12	chr6:87380671-87380721	ECC-1	luminal epithelium:	n/a
13	chr6:87380615-87380665	Caco-2	colon:	n/a
14	chr6:87380615-87380665	GM19239	blood:	n/a
15	chr6:87380671-87380721	BE2_C	brain:	n/a
16	chr6:87380615-87380665	ProgFib	skin:	n/a
17	chr6:87466574-87466624	HMEC	breast:	n/a
18	chr6:87380615-87380665	HMEC	breast:	n/a
19	chr6:87380671-87380721	PFSK-1	brain:	n/a
20	chr6:87466574-87466624	RPTEC	kidney:	n/a
21	chr6:87380671-87380721	AG09319	gingival:	n/a
22	chr6:87380615-87380665	BE2_C	brain:	n/a
23	chr6:87380615-87380665	Hela-S3	cervix:	n/a
24	chr6:87380671-87380721	Hela-S3	cervix:	n/a
25	chr6:87380615-87380665	IMR90	lung:	fetal
26	chr6:87466574-87466624	GM19239	blood:	n/a
27	chr6:87380671-87380721	MCF-7	breast:	n/a
28	chr6:87466574-87466624	HRPEpiC	eye:	n/a
29	chr6:87380671-87380721	HUVEC	blood vessel:	n/a
30	chr6:87466574-87466624	GM12891	blood:	n/a
31	chr6:87380671-87380721	H1-hESC	embryonic stem cell:	embryo
32	chr6:87466574-87466624	NT2-D1	testis:	n/a
33	chr6:87466574-87466624	SK-N-SH_RA	brain:	n/a
34	chr6:87380671-87380721	NT2-D1	testis:	n/a
35	chr6:87466574-87466624	IMR90	lung:	fetal
36	chr6:87466574-87466624	T-47D	breast:	n/a
37	chr6:87380615-87380665	HUVEC	blood vessel:	n/a
38	chr6:87466574-87466624	Caco-2	colon:	n/a
39	chr6:87380671-87380721	U87	brain:	n/a
40	chr6:87466574-87466624	HRE	kidney:	n/a
41	chr6:87380671-87380721	SK-N-MC	brain:	n/a
42	chr6:87466574-87466624	HEEpiC	esophagus:	n/a
43	chr6:87380615-87380665	ovcar-3	ovarian:	n/a
44	chr6:87380615-87380665	MCF-7	breast:	n/a
45	chr6:87466574-87466624	SK-N-SH	brain:	n/a
46	chr6:87380671-87380721	PANC-1	pancreas:	n/a
47	chr6:87466574-87466624	NH-A	brain:	n/a
48	chr6:87380671-87380721	SKMC	muscle:	n/a
49	chr6:87466574-87466624	LNCaP	prostate:	n/a
50	chr6:87380615-87380665	GM12891	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:87433212..87433993-chr6:87487281..87488109,4	MCF-7	breast:
2	chr6:87433963..87436868-chr6:87437226..87439496,2	K562	blood:
3	chr6:87432080..87434373-chr6:87487910..87490262,2	MCF-7	breast:
4	chr6:87424582..87427120-chr6:87432105..87434756,2	MCF-7	breast:
5	chr6:86352318..86354176-chr6:87391935..87394056,2	K562	blood:
6	chr6:87424582..87427120-chr6:87432105..87434756,2	MCF-7	breast:
7	chr6:87423786..87425445-chr6:87431347..87433792,2	MCF-7	breast:
8	chr6:87433852..87435934-chr6:87437670..87440817,3	MCF-7	breast:
9	chr6:87423786..87425445-chr6:87431347..87433792,2	MCF-7	breast:
10	chr13:44659379..44659987-chr6:87449509..87450364,2	MCF-7	breast:
11	chr6:87433571..87436009-chr6:87486240..87488175,2	MCF-7	breast:
12	chr6:87433963..87436868-chr6:87437226..87439496,2	K562	blood:
13	chr6:86386556..86388965-chr6:87417224..87418892,2	MCF-7	breast:
14	chr6:87317696..87319542-chr6:87392510..87394797,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGA-7	chr6:87439426-87439826	NONHSAT113883

No data

Variant related genes	Relation type
ENSG00000218561	TF binding region
ENSG00000218561	CpG island
ENSG00000135316	chromatin interactions
ENSG00000218561	chromatin interactions
ENSG00000203875	chromatin interactions

Extended variants
information (count: 2966 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:2966 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143421466	chr6:87350202-87350203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375671172	chr6:87350239-87350240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182158471	chr6:87350261-87350262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2324950	chr6:87350271-87350272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs561353178	chr6:87350288-87350289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528858299	chr6:87350310-87350311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376088791	chr6:87350315-87350316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370333607	chr6:87350318-87350319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376828362	chr6:87350326-87350327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367699705	chr6:87350327-87350328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs67929946	chr6:87350328-87350329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386703479	chr6:87350329-87350330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548232908	chr6:87350352-87350353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185583810	chr6:87350377-87350378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs386703480	chr6:87350378-87350379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148173066	chr6:87350458-87350459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573435922	chr6:87350459-87350460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551695134	chr6:87350465-87350466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560692395	chr6:87350515-87350516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527788975	chr6:87350529-87350530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568183524	chr6:87350533-87350534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549494828	chr6:87350538-87350539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567702207	chr6:87350595-87350596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538755447	chr6:87350601-87350602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189999712	chr6:87350615-87350616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550880923	chr6:87350616-87350617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183738975	chr6:87350641-87350642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539685722	chr6:87350659-87350660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533765536	chr6:87350761-87350762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141982537	chr6:87350839-87350840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553536011	chr6:87350868-87350869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572949358	chr6:87350870-87350871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150675565	chr6:87350894-87350895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558659047	chr6:87350907-87350908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7453325	chr6:87350911-87350912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573337930	chr6:87350941-87350942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543824270	chr6:87350944-87350945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139219952	chr6:87350951-87350952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs578192503	chr6:87350962-87350963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545634419	chr6:87350979-87350980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373746416	chr6:87350980-87350981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35053960	chr6:87351039-87351040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs16877571	chr6:87351067-87351068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549531571	chr6:87351069-87351070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561346061	chr6:87351086-87351087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147480909	chr6:87351089-87351090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368057596	chr6:87351112-87351113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549923977	chr6:87351148-87351149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571576173	chr6:87351157-87351158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539355936	chr6:87351161-87351162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
craniofacial dysmorphism	21918468	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	19490664	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:87350200-87354400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:87354400-87354600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:87368400-87368800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:87374000-87374600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:87381000-87386600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:87381600-87382400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:87386600-87387600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:87387600-87388200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:87388000-87389800	Enhancers	K562	blood
10	chr6:87388200-87390600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:87389800-87391400	Weak transcription	K562	blood
12	chr6:87390600-87391600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:87391400-87392000	Enhancers	K562	blood
14	chr6:87392000-87393200	Flanking Active TSS	K562	blood
15	chr6:87392200-87393600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:87393200-87393600	Enhancers	K562	blood
17	chr6:87393600-87394000	Flanking Active TSS	K562	blood
18	chr6:87394000-87394600	Enhancers	K562	blood
19	chr6:87394600-87394800	Flanking Active TSS	K562	blood
20	chr6:87394600-87396000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr6:87394800-87396600	Enhancers	K562	blood
22	chr6:87396000-87396400	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr6:87398600-87399000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:87405800-87406000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:87406000-87410200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:87409600-87410600	Enhancers	K562	blood
27	chr6:87410200-87412400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:87412400-87412800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:87412400-87413000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr6:87412800-87413200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:87413200-87413400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:87413400-87413800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:87415600-87416000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr6:87416000-87416400	Enhancers	Placenta	Placenta
35	chr6:87416000-87416800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:87416000-87421400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr6:87418800-87419000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:87419000-87421600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr6:87421200-87422000	Enhancers	K562	blood
40	chr6:87421400-87422000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr6:87421400-87422200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:87421600-87422000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr6:87421600-87422000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:87421800-87422200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr6:87421800-87422400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr6:87422000-87425600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr6:87422200-87425000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr6:87423400-87428600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:87425000-87425400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr6:87428200-87429400	Weak transcription	H1 Cell Line	embryonic stem cell

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