Variant report

Variant	nsv603600
Chromosome Location	chr6:68526511-68601405
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:541)
CpG islands
(count:1528)
Chromatin interactive
region (count:109)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:68586588-68586875	K562	blood:	n/a	n/a
2	ARID3A	chr6:68585707-68586266	K562	blood:	n/a	n/a
3	ARID3A	chr6:68597363-68597629	K562	blood:	n/a	n/a
4	ARID3A	chr6:68591745-68592369	K562	blood:	n/a	n/a
5	ARID3A	chr6:68587287-68587821	K562	blood:	n/a	n/a
6	ARID3A	chr6:68590846-68591312	K562	blood:	n/a	n/a
7	ARID3A	chr6:68588859-68589349	K562	blood:	n/a	n/a
8	ARID3A	chr6:68598616-68600400	K562	blood:	n/a	n/a
9	ATF1	chr6:68598554-68599440	K562	blood:	n/a	n/a
10	ATF1	chr6:68590947-68591336	K562	blood:	n/a	n/a
11	ATF1	chr6:68576431-68576606	K562	blood:	n/a	n/a
12	ATF1	chr6:68592444-68592941	K562	blood:	n/a	n/a
13	ATF3	chr6:68598808-68599434	K562	blood:	n/a	n/a
14	BACH1	chr6:68598800-68599114	K562	blood:	n/a	n/a
15	BACH1	chr6:68585892-68586249	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:68588913-68589303	K562	blood:	n/a	n/a
17	BACH1	chr6:68585758-68586506	K562	blood:	n/a	n/a
18	BCL3	chr6:68590214-68590374	K562	blood:	n/a	n/a
19	BCL3	chr6:68598839-68599484	K562	blood:	n/a	n/a
20	BCL3	chr6:68588561-68589454	K562	blood:	n/a	n/a
21	BCL3	chr6:68590567-68590728	K562	blood:	n/a	n/a
22	BCL3	chr6:68591148-68591620	K562	blood:	n/a	n/a
23	BCL3	chr6:68590634-68591815	K562	blood:	n/a	n/a
24	BCL3	chr6:68590756-68591131	K562	blood:	n/a	n/a
25	BCLAF1	chr6:68597199-68599447	K562	blood:	n/a	n/a
26	BCLAF1	chr6:68594905-68596425	K562	blood:	n/a	n/a
27	BCLAF1	chr6:68596665-68599377	K562	blood:	n/a	n/a
28	BCLAF1	chr6:68590734-68592419	K562	blood:	n/a	n/a
29	BCLAF1	chr6:68590647-68592475	K562	blood:	n/a	n/a
30	BCLAF1	chr6:68594048-68594775	K562	blood:	n/a	n/a
31	BHLHE40	chr6:68590943-68591320	K562	blood:	n/a	n/a
32	BHLHE40	chr6:68595340-68595613	K562	blood:	n/a	n/a
33	BHLHE40	chr6:68597358-68599424	K562	blood:	n/a	n/a
34	BHLHE40	chr6:68591700-68592029	K562	blood:	n/a	n/a
35	CBX3	chr6:68566562-68566946	K562	blood:	n/a	n/a
36	CBX3	chr6:68590777-68591677	K562	blood:	n/a	n/a
37	CBX3	chr6:68590808-68591319	K562	blood:	n/a	n/a
38	CBX3	chr6:68598539-68599422	K562	blood:	n/a	n/a
39	CBX3	chr6:68598810-68599526	K562	blood:	n/a	n/a
40	CBX3	chr6:68549756-68550082	K562	blood:	n/a	n/a
41	CBX3	chr6:68530161-68530596	K562	blood:	n/a	n/a
42	CBX3	chr6:68549722-68550040	K562	blood:	n/a	n/a
43	CBX3	chr6:68531586-68531842	K562	blood:	n/a	n/a
44	CBX3	chr6:68597615-68598167	K562	blood:	n/a	n/a
45	CCNT2	chr6:68588617-68589367	K562	blood:	n/a	n/a
46	CCNT2	chr6:68596850-68597436	K562	blood:	n/a	n/a
47	CCNT2	chr6:68594337-68595549	K562	blood:	n/a	n/a
48	CCNT2	chr6:68593085-68593955	K562	blood:	n/a	n/a
49	CCNT2	chr6:68590125-68590324	K562	blood:	n/a	n/a
50	CCNT2	chr6:68597646-68599928	K562	blood:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:68597649-68597699	AG10803	skin:	n/a
2	chr6:68596739-68596789	HCT-116	colon:	n/a
3	chr6:68599280-68599330	MCF10A-Er-Src	breast:	n/a
4	chr6:68597649-68597699	AG10803	skin:	n/a
5	chr6:68596739-68596789	HCT-116	colon:	n/a
6	chr6:68599280-68599330	MCF10A-Er-Src	breast:	n/a
7	chr6:68596739-68596789	NB4	blood:	n/a
8	chr6:68598642-68598692	NHDF-neo	bronchial:	n/a
9	chr6:68597649-68597699	NB4	blood:	n/a
10	chr6:68599358-68599408	HCF	heart:	n/a
11	chr6:68598701-68598751	HIPEpiC	eye:	n/a
12	chr6:68595695-68595745	ovcar-3	ovarian:	n/a
13	chr6:68595814-68595864	SK-N-SH	brain:	n/a
14	chr6:68598790-68598840	HRPEpiC	eye:	n/a
15	chr6:68599196-68599246	AG09319	gingival:	n/a
16	chr6:68596920-68596970	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:68598790-68598840	ovcar-3	ovarian:	n/a
18	chr6:68598701-68598751	Hepatocyte	liver:	n/a
19	chr6:68595547-68595597	MCF-7	breast:	n/a
20	chr6:68535253-68535303	HepG2	liver:	n/a
21	chr6:68599358-68599408	PFSK-1	brain:	n/a
22	chr6:68595695-68595745	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:68597705-68597755	H1-hESC	embryonic stem cell:	embryo
24	chr6:68596739-68596789	HNPCEpiC	eye:	n/a
25	chr6:68596887-68596937	A549	lung:	n/a
26	chr6:68535253-68535303	HNPCEpiC	eye:	n/a
27	chr6:68596945-68596995	BJ	skin:	n/a
28	chr6:68599196-68599246	SK-N-SH_RA	brain:	n/a
29	chr6:68596644-68596694	AG04450	lung:	fetal
30	chr6:68535378-68535428	AG04450	lung:	fetal
31	chr6:68595695-68595745	Hepatocyte	liver:	n/a
32	chr6:68596851-68596901	ProgFib	skin:	n/a
33	chr6:68598701-68598751	ProgFib	skin:	n/a
34	chr6:68596880-68596930	NH-A	brain:	n/a
35	chr6:68598701-68598751	HepG2	liver:	n/a
36	chr6:68598790-68598840	NHBE	bronchial:	n/a
37	chr6:68597649-68597699	HMEC	breast:	n/a
38	chr6:68598701-68598751	GM12891	blood:	n/a
39	chr6:68596851-68596901	SK-N-SH_RA	brain:	n/a
40	chr6:68595695-68595745	HRE	kidney:	n/a
41	chr6:68595814-68595864	PrEC	prostate:	n/a
42	chr6:68596851-68596901	HEK293	kidney:	embryo
43	chr6:68598790-68598840	NT2-D1	testis:	n/a
44	chr6:68595425-68595475	U87	brain:	n/a
45	chr6:68598642-68598692	Hepatocyte	liver:	n/a
46	chr6:68598642-68598692	ProgFib	skin:	n/a
47	chr6:68596887-68596937	NHBE	bronchial:	n/a
48	chr6:68595789-68595839	IMR90	lung:	fetal
49	chr6:68596945-68596995	HCT-116	colon:	n/a
50	chr6:68595547-68595597	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:68595949..68597859-chr6:68734375..68736391,2	K562	blood:
2	chr6:68595545..68597855-chr6:68811706..68813567,2	K562	blood:
3	chr6:68592636..68595317-chr6:68948923..68950964,2	K562	blood:
4	chr6:68590714..68592952-chr6:68747177..68749735,2	K562	blood:
5	chr6:68568907..68571616-chr6:68584376..68587253,2	K562	blood:
6	chr6:68547547..68550357-chr6:68551915..68554138,2	K562	blood:
7	chr6:68594102..68595844-chr6:68652548..68654893,2	K562	blood:
8	chr6:68573446..68581402-chr6:68582909..68592336,10	K562	blood:
9	chr6:68556597..68558749-chr6:68589649..68591712,2	K562	blood:
10	chr6:68593412..68595516-chr6:68761853..68764592,2	K562	blood:
11	chr6:68573446..68581402-chr6:68582909..68592336,10	K562	blood:
12	chr6:68569432..68571622-chr6:68584062..68586266,2	K562	blood:
13	chr6:68567182..68570934-chr6:68589376..68594123,5	K562	blood:
14	chr6:68592548..68595434-chr6:68676604..68678342,2	K562	blood:
15	chr6:68547444..68549949-chr6:68573736..68576048,2	K562	blood:
16	chr6:68590859..68593672-chr6:68895992..68897961,2	K562	blood:
17	chr6:68487893..68492102-chr6:68589175..68592601,3	K562	blood:
18	chr6:68590833..68592511-chr6:68938075..68940408,2	K562	blood:
19	chr6:68310865..68312507-chr6:68587249..68589737,2	K562	blood:
20	chr6:68547444..68549949-chr6:68573736..68576048,2	K562	blood:
21	chr6:68568907..68571616-chr6:68584376..68587253,2	K562	blood:
22	chr6:68536799..68539603-chr6:68596388..68598397,3	K562	blood:
23	chr6:68524696..68527384-chr6:68621549..68624145,2	K562	blood:
24	chr6:68595593..68598557-chr6:68689964..68691927,2	K562	blood:
25	chr6:68540202..68542998-chr6:68546764..68550157,3	K562	blood:
26	chr6:68536915..68539495-chr6:68589360..68592356,2	K562	blood:
27	chr6:66834810..66837020-chr6:68592934..68595671,2	K562	blood:
28	chr6:68526302..68528861-chr6:68589290..68590990,2	K562	blood:
29	chr6:68596749..68599192-chr6:68783543..68786412,2	K562	blood:
30	chr6:68593975..68595593-chr6:68783450..68785952,2	K562	blood:
31	chr6:68590248..68591834-chr6:68753990..68756247,2	K562	blood:
32	chr6:67961598..67964297-chr6:68597509..68599037,2	K562	blood:
33	chr6:68596440..68599032-chr6:68647248..68649168,3	K562	blood:
34	chr6:68591172..68594136-chr6:68947672..68950423,2	K562	blood:
35	chr6:68543570..68546235-chr6:68549080..68552286,3	K562	blood:
36	chr6:68537029..68538860-chr6:68542513..68544423,2	K562	blood:
37	chr6:68384869..68387346-chr6:68589720..68591224,2	K562	blood:
38	chr6:68564294..68566367-chr6:68570127..68572578,2	MCF-7	breast:
39	chr6:68599985..68602713-chr6:68605698..68607333,2	MCF-7	breast:
40	chr6:68586431..68588807-chr6:68750626..68752496,2	K562	blood:
41	chr6:68361466..68364465-chr6:68587796..68590691,2	K562	blood:
42	chr6:68587589..68589412-chr6:68801238..68803504,2	K562	blood:
43	chr6:68546534..68549959-chr6:68591405..68594115,3	K562	blood:
44	chr6:68595949..68597859-chr6:68734333..68736391,3	K562	blood:
45	chr6:68556597..68558749-chr6:68589649..68591712,2	K562	blood:
46	chr6:68403017..68405900-chr6:68588028..68590720,2	K562	blood:
47	chr10:129266757..129267591-chr6:68536748..68537711,2	NB4	blood:
48	chr6:68540202..68542998-chr6:68546764..68550157,3	K562	blood:
49	chr6:68596878..68598658-chr6:68612874..68615713,2	K562	blood:
50	chr6:68543570..68546235-chr6:68549080..68552286,3	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
ENSG00000270509	chromatin interactions

Extended variants
information (count: 1758 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1758 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1913477	chr6:68526511-68526512	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373686788	chr6:68526548-68526549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544973565	chr6:68526621-68526622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146810176	chr6:68526636-68526637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527736727	chr6:68526653-68526654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs386702341	chr6:68526679-68526680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80348190	chr6:68526693-68526694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561318370	chr6:68526697-68526698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530355836	chr6:68526699-68526700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373765817	chr6:68526713-68526714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1913478	chr6:68526716-68526717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs140464690	chr6:68526734-68526735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150401372	chr6:68526751-68526752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552170701	chr6:68526752-68526753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565689649	chr6:68526779-68526780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138115469	chr6:68526791-68526792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149113603	chr6:68526805-68526806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543265871	chr6:68526843-68526844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183659310	chr6:68526845-68526846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563532244	chr6:68526855-68526856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73444607	chr6:68526888-68526889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs576691687	chr6:68526893-68526894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75457777	chr6:68526926-68526927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13215798	chr6:68526949-68526950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs572152635	chr6:68526963-68526964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541116016	chr6:68526978-68526979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368283572	chr6:68526995-68526996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561465025	chr6:68527032-68527033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187905022	chr6:68527050-68527051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543969760	chr6:68527053-68527054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370362760	chr6:68527082-68527083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192325571	chr6:68527095-68527096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532817070	chr6:68527109-68527110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552907596	chr6:68527130-68527131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146076641	chr6:68527147-68527148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528133869	chr6:68527160-68527161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547962659	chr6:68527167-68527168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183629012	chr6:68527169-68527170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536762298	chr6:68527220-68527221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550708974	chr6:68527235-68527236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113087224	chr6:68527287-68527288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539342270	chr6:68527381-68527382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186557699	chr6:68527409-68527410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572090211	chr6:68527426-68527427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535048151	chr6:68527455-68527456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554689960	chr6:68527528-68527529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373561269	chr6:68527576-68527577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368081358	chr6:68527607-68527608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62412353	chr6:68527646-68527647	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs543564187	chr6:68527664-68527665	Weak transcription	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:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:68526000-68527000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:68527000-68527600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:68527400-68527600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:68527600-68538200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:68535400-68535600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:68535600-68537400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:68538200-68538400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:68543600-68545000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:68543600-68545000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr6:68543600-68545200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr6:68543600-68545400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr6:68543800-68545000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr6:68544200-68544800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr6:68544400-68544800	Enhancers	K562	blood
15	chr6:68544400-68545200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr6:68544600-68545000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr6:68544600-68545000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr6:68549200-68549600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:68556600-68559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:68557800-68558200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:68563800-68564200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:68564000-68564400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:68581600-68586200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:68583800-68584000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:68585800-68586200	Enhancers	Adipose Nuclei	Adipose
26	chr6:68585800-68589400	Enhancers	K562	blood
27	chr6:68587400-68588000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr6:68588200-68588600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr6:68588600-68589000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr6:68589000-68589200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:68589200-68591200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:68589400-68590800	Weak transcription	K562	blood
33	chr6:68590800-68591000	ZNF genes & repeats	K562	blood
34	chr6:68591000-68591600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:68591000-68591600	Enhancers	Hela-S3	cervix
36	chr6:68591000-68591800	Enhancers	NH-A	brain
37	chr6:68591000-68598400	Transcr. at gene 5' and 3'	K562	blood
38	chr6:68591200-68592000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr6:68591400-68596800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:68591600-68591800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr6:68591800-68595000	Weak transcription	NH-A	brain
42	chr6:68592000-68596600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:68595000-68595600	Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr6:68598200-68599000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:68598400-68598800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
46	chr6:68598400-68601400	Active TSS	K562	blood
47	chr6:68598600-68599200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:68598800-68599200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:68598800-68599600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr6:68598800-68599800	Enhancers	Hela-S3	cervix

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