Variant report

Variant	esv3368842
Chromosome Location	chr6:68544280-68616669
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:596)
CpG islands
(count:1404)
Chromatin interactive
region (count:109)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:68588859-68589349	K562	blood:	n/a	n/a
2	ARID3A	chr6:68608793-68609251	K562	blood:	n/a	n/a
3	ARID3A	chr6:68591745-68592369	K562	blood:	n/a	n/a
4	ARID3A	chr6:68598616-68600400	K562	blood:	n/a	n/a
5	ARID3A	chr6:68586588-68586875	K562	blood:	n/a	n/a
6	ARID3A	chr6:68585707-68586266	K562	blood:	n/a	n/a
7	ARID3A	chr6:68597363-68597629	K562	blood:	n/a	n/a
8	ARID3A	chr6:68587287-68587821	K562	blood:	n/a	n/a
9	ARID3A	chr6:68590846-68591312	K562	blood:	n/a	n/a
10	ATF1	chr6:68592444-68592941	K562	blood:	n/a	n/a
11	ATF1	chr6:68606467-68606690	K562	blood:	n/a	n/a
12	ATF1	chr6:68590947-68591336	K562	blood:	n/a	n/a
13	ATF1	chr6:68576431-68576606	K562	blood:	n/a	n/a
14	ATF1	chr6:68598554-68599440	K562	blood:	n/a	n/a
15	ATF1	chr6:68608783-68609230	K562	blood:	n/a	n/a
16	ATF3	chr6:68606439-68606788	K562	blood:	n/a	n/a
17	ATF3	chr6:68598808-68599434	K562	blood:	n/a	n/a
18	BACH1	chr6:68598800-68599114	K562	blood:	n/a	n/a
19	BACH1	chr6:68585892-68586249	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:68606755-68606885	K562	blood:	n/a	n/a
21	BACH1	chr6:68588913-68589303	K562	blood:	n/a	n/a
22	BACH1	chr6:68585758-68586506	K562	blood:	n/a	n/a
23	BCL3	chr6:68591148-68591620	K562	blood:	n/a	n/a
24	BCL3	chr6:68590634-68591815	K562	blood:	n/a	n/a
25	BCL3	chr6:68590756-68591131	K562	blood:	n/a	n/a
26	BCL3	chr6:68590567-68590728	K562	blood:	n/a	n/a
27	BCL3	chr6:68588561-68589454	K562	blood:	n/a	n/a
28	BCL3	chr6:68590214-68590374	K562	blood:	n/a	n/a
29	BCL3	chr6:68598839-68599484	K562	blood:	n/a	n/a
30	BCLAF1	chr6:68594905-68596425	K562	blood:	n/a	n/a
31	BCLAF1	chr6:68596665-68599377	K562	blood:	n/a	n/a
32	BCLAF1	chr6:68590647-68592475	K562	blood:	n/a	n/a
33	BCLAF1	chr6:68594048-68594775	K562	blood:	n/a	n/a
34	BCLAF1	chr6:68597199-68599447	K562	blood:	n/a	n/a
35	BCLAF1	chr6:68590734-68592419	K562	blood:	n/a	n/a
36	BHLHE40	chr6:68595340-68595613	K562	blood:	n/a	n/a
37	BHLHE40	chr6:68607929-68608540	K562	blood:	n/a	n/a
38	BHLHE40	chr6:68597358-68599424	K562	blood:	n/a	n/a
39	BHLHE40	chr6:68590943-68591320	K562	blood:	n/a	n/a
40	BHLHE40	chr6:68591700-68592029	K562	blood:	n/a	n/a
41	CBX3	chr6:68608679-68609139	K562	blood:	n/a	n/a
42	CBX3	chr6:68597615-68598167	K562	blood:	n/a	n/a
43	CBX3	chr6:68598810-68599526	K562	blood:	n/a	n/a
44	CBX3	chr6:68606363-68606676	K562	blood:	n/a	n/a
45	CBX3	chr6:68566562-68566946	K562	blood:	n/a	n/a
46	CBX3	chr6:68590777-68591677	K562	blood:	n/a	n/a
47	CBX3	chr6:68614620-68615055	K562	blood:	n/a	n/a
48	CBX3	chr6:68549722-68550040	K562	blood:	n/a	n/a
49	CBX3	chr6:68549756-68550082	K562	blood:	n/a	n/a
50	CBX3	chr6:68598539-68599422	K562	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:68597028-68597078	HCPEpiC	choroid plexus:	n/a
2	chr6:68597028-68597078	HCPEpiC	choroid plexus:	n/a
3	chr6:68596880-68596930	HIPEpiC	eye:	n/a
4	chr6:68596880-68596930	AoSMC	blood vessel:	n/a
5	chr6:68598701-68598751	MCF10A-Er-Src	breast:	n/a
6	chr6:68597649-68597699	AG09319	gingival:	n/a
7	chr6:68598701-68598751	AG09319	gingival:	n/a
8	chr6:68598642-68598692	Caco-2	colon:	n/a
9	chr6:68595789-68595839	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:68596739-68596789	AG10803	skin:	n/a
11	chr6:68598790-68598840	HCF	heart:	n/a
12	chr6:68595789-68595839	BJ	skin:	n/a
13	chr6:68599196-68599246	SAEC	small airway:	n/a
14	chr6:68596920-68596970	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:68596880-68596930	HAEpiC	amniotic membrane:	n/a
16	chr6:68598642-68598692	HUVEC	blood vessel:	n/a
17	chr6:68597649-68597699	HMEC	breast:	n/a
18	chr6:68598701-68598751	ECC-1	luminal epithelium:	n/a
19	chr6:68598642-68598692	MCF-7	breast:	n/a
20	chr6:68595789-68595839	LNCaP	prostate:	n/a
21	chr6:68595789-68595839	SKMC	muscle:	n/a
22	chr6:68598858-68598908	NHBE	bronchial:	n/a
23	chr6:68599358-68599408	GM12892	blood:	n/a
24	chr6:68596739-68596789	HRPEpiC	eye:	n/a
25	chr6:68595814-68595864	GM12891	blood:	n/a
26	chr6:68596920-68596970	Hela-S3	cervix:	n/a
27	chr6:68595814-68595864	HMEC	breast:	n/a
28	chr6:68595814-68595864	HepG2	liver:	n/a
29	chr6:68598701-68598751	U87	brain:	n/a
30	chr6:68598701-68598751	IMR90	lung:	fetal
31	chr6:68599129-68599179	HAEpiC	amniotic membrane:	n/a
32	chr6:68598642-68598692	GM12878	blood:	n/a
33	chr6:68597649-68597699	HCF	heart:	n/a
34	chr6:68596887-68596937	Caco-2	colon:	n/a
35	chr6:68595789-68595839	A549	lung:	n/a
36	chr6:68598701-68598751	HL-60	blood:	n/a
37	chr6:68596880-68596930	PFSK-1	brain:	n/a
38	chr6:68598790-68598840	HEEpiC	esophagus:	n/a
39	chr6:68599280-68599330	ProgFib	skin:	n/a
40	chr6:68595695-68595745	HRPEpiC	eye:	n/a
41	chr6:68597705-68597755	SKMC	muscle:	n/a
42	chr6:68598790-68598840	HNPCEpiC	eye:	n/a
43	chr6:68596851-68596901	AoSMC	blood vessel:	n/a
44	chr6:68597649-68597699	U87	brain:	n/a
45	chr6:68596920-68596970	AG10803	skin:	n/a
46	chr6:68598642-68598692	HEEpiC	esophagus:	n/a
47	chr6:68595547-68595597	AoSMC	blood vessel:	n/a
48	chr6:68596739-68596789	GM06990	blood:	n/a
49	chr6:68599358-68599408	NHBE	bronchial:	n/a
50	chr6:68597028-68597078	GM19239	blood:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:68595949..68597859-chr6:68734333..68736391,3	K562	blood:
2	chr6:68556597..68558749-chr6:68589649..68591712,2	K562	blood:
3	chr6:68568907..68571616-chr6:68584376..68587253,2	K562	blood:
4	chr6:66834810..66837020-chr6:68592934..68595671,2	K562	blood:
5	chr6:68587425..68594562-chr6:68930728..68938009,10	K562	blood:
6	chr6:68543570..68546235-chr6:68549080..68552286,3	K562	blood:
7	chr6:68590248..68591834-chr6:68753990..68756247,2	K562	blood:
8	chr6:68597158..68599225-chr6:68614213..68617190,2	K562	blood:
9	chr6:68595612..68597552-chr6:68616744..68619642,2	K562	blood:
10	chr6:68502919..68505150-chr6:68587246..68590550,4	K562	blood:
11	chr6:68596440..68599032-chr6:68647248..68649168,3	K562	blood:
12	chr6:68487636..68489959-chr6:68585344..68587572,2	K562	blood:
13	chr6:68536915..68539495-chr6:68589360..68592356,2	K562	blood:
14	chr6:68593774..68595835-chr6:68943897..68947286,3	K562	blood:
15	chr6:68506908..68510214-chr6:68588930..68590665,3	K562	blood:
16	chr6:68580821..68583370-chr6:68587245..68588979,2	K562	blood:
17	chr6:68547444..68549949-chr6:68573736..68576048,2	K562	blood:
18	chr6:68546534..68549959-chr6:68591405..68594115,3	K562	blood:
19	chr6:68571923..68574390-chr6:68700844..68702583,2	K562	blood:
20	chr6:68562527..68565215-chr6:68588017..68590595,2	K562	blood:
21	chr6:68595545..68597855-chr6:68811706..68813567,2	K562	blood:
22	chr6:68599985..68602713-chr6:68605698..68607333,2	MCF-7	breast:
23	chr6:68596140..68598013-chr6:68631347..68633345,2	K562	blood:
24	chr6:68592315..68594490-chr6:68729157..68731583,2	K562	blood:
25	chr6:68311734..68314302-chr6:68583935..68586240,2	K562	blood:
26	chr6:68564294..68566367-chr6:68570127..68572578,2	MCF-7	breast:
27	chr6:68606092..68608064-chr6:68618908..68621057,2	K562	blood:
28	chr6:68593975..68595593-chr6:68783450..68785952,2	K562	blood:
29	chr6:68361466..68364465-chr6:68587796..68590691,2	K562	blood:
30	chr6:68604107..68606709-chr6:68609617..68614181,4	K562	blood:
31	chr6:68569432..68571622-chr6:68584062..68586266,2	K562	blood:
32	chr6:68596878..68598658-chr6:68612874..68615713,2	K562	blood:
33	chr6:68604107..68606709-chr6:68609617..68614181,4	K562	blood:
34	chr6:68595949..68597859-chr6:68734375..68736391,2	K562	blood:
35	chr6:68569432..68571622-chr6:68584062..68586266,2	K562	blood:
36	chr6:68607711..68610466-chr6:68621509..68623559,2	K562	blood:
37	chr6:68586431..68588807-chr6:68750626..68752496,2	K562	blood:
38	chr6:68590714..68592952-chr6:68747177..68749735,2	K562	blood:
39	chr6:68604720..68607895-chr6:68608418..68610279,3	K562	blood:
40	chr6:68592548..68595434-chr6:68676604..68678342,2	K562	blood:
41	chr6:68562527..68565215-chr6:68588017..68590595,2	K562	blood:
42	chr6:68585867..68587993-chr6:68750616..68752960,3	K562	blood:
43	chr6:67796143..67796843-chr6:68573181..68573682,2	MCF-7	breast:
44	chr6:68590326..68593646-chr6:68740813..68742652,3	K562	blood:
45	chr6:68590859..68593672-chr6:68895992..68897961,2	K562	blood:
46	chr6:68540202..68542998-chr6:68546764..68550157,3	K562	blood:
47	chr6:68567182..68570934-chr6:68589376..68594123,5	K562	blood:
48	chr6:68596749..68599192-chr6:68783543..68786412,2	K562	blood:
49	chr6:68593412..68595516-chr6:68761853..68764592,2	K562	blood:
50	chr6:68591162..68594007-chr9:94838364..94841394,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL713998.1-3	chr6:68597538-68598713	ENSG00000227706.3
2	lnc-AL713998.1-3	chr6:68598803-68599231	ENSG00000227706.3

No data

Variant related genes	Relation type
ENSG00000227706	TF binding region
ENSG00000227706	CpG island
ENSG00000227706	chromatin interactions
ENSG00000270509	chromatin interactions

Extended variants
information (count: 1591 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561188692	chr6:68544305-68544306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570555223	chr6:68544307-68544308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566840047	chr6:68544317-68544318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183130220	chr6:68544321-68544322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71536427	chr6:68544324-68544325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548704674	chr6:68544332-68544333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114716417	chr6:68544348-68544349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148816851	chr6:68544365-68544366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557928027	chr6:68544379-68544380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571495482	chr6:68544380-68544381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534063596	chr6:68544395-68544396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187709631	chr6:68544415-68544416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574002362	chr6:68544421-68544422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542158211	chr6:68544437-68544438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192775671	chr6:68544450-68544451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182530671	chr6:68544536-68544537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575692829	chr6:68544549-68544550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544408330	chr6:68544556-68544557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564327747	chr6:68544562-68544563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533318649	chr6:68544594-68544595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540448348	chr6:68544656-68544657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79891340	chr6:68544671-68544672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147952909	chr6:68544709-68544710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141797555	chr6:68544712-68544713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188293035	chr6:68544738-68544739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373197620	chr6:68544781-68544782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147088233	chr6:68544787-68544788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551220975	chr6:68544816-68544817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138442249	chr6:68544817-68544818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192524371	chr6:68544825-68544826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141898139	chr6:68544866-68544867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs62414263	chr6:68544868-68544869	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs150211339	chr6:68544874-68544875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555712558	chr6:68544875-68544876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184608296	chr6:68544885-68544886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77631613	chr6:68544888-68544889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188932844	chr6:68544908-68544909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138735654	chr6:68544924-68544925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540388609	chr6:68544933-68544934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560355624	chr6:68545018-68545019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543031472	chr6:68545072-68545073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562906516	chr6:68545073-68545074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529586788	chr6:68545078-68545079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542977935	chr6:68545106-68545107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562489202	chr6:68545165-68545166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531820726	chr6:68545181-68545182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531173360	chr6:68545200-68545201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114740288	chr6:68545209-68545210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551825925	chr6:68545216-68545217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192093438	chr6:68545238-68545239	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	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
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:68543600-68545000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr6:68543600-68545000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr6:68543600-68545200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:68543600-68545400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr6:68543800-68545000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr6:68544200-68544800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr6:68544400-68544800	Enhancers	K562	blood
8	chr6:68544400-68545200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:68544600-68545000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr6:68544600-68545000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr6:68549200-68549600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:68556600-68559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:68557800-68558200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:68563800-68564200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:68564000-68564400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:68581600-68586200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:68583800-68584000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:68585800-68586200	Enhancers	Adipose Nuclei	Adipose
19	chr6:68585800-68589400	Enhancers	K562	blood
20	chr6:68587400-68588000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr6:68588200-68588600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:68588600-68589000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:68589000-68589200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:68589200-68591200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:68589400-68590800	Weak transcription	K562	blood
26	chr6:68590800-68591000	ZNF genes & repeats	K562	blood
27	chr6:68591000-68591600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:68591000-68591600	Enhancers	Hela-S3	cervix
29	chr6:68591000-68591800	Enhancers	NH-A	brain
30	chr6:68591000-68598400	Transcr. at gene 5' and 3'	K562	blood
31	chr6:68591200-68592000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:68591400-68596800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:68591600-68591800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:68591800-68595000	Weak transcription	NH-A	brain
35	chr6:68592000-68596600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:68595000-68595600	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr6:68598200-68599000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:68598400-68598800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
39	chr6:68598400-68601400	Active TSS	K562	blood
40	chr6:68598600-68599200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr6:68598800-68599200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:68598800-68599600	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr6:68598800-68599800	Enhancers	Hela-S3	cervix
44	chr6:68598800-68600200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:68599000-68599200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr6:68599200-68599800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:68599600-68607800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr6:68599800-68600200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr6:68600000-68601400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr6:68600200-68600600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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