Variant report

Variant	nsv1030673
Chromosome Location	chr6:68545302-68642745
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:1406)
Chromatin interactive
region (count:120)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:68591745-68592369	K562	blood:	n/a	n/a
2	ARID3A	chr6:68590846-68591312	K562	blood:	n/a	n/a
3	ARID3A	chr6:68608793-68609251	K562	blood:	n/a	n/a
4	ARID3A	chr6:68586588-68586875	K562	blood:	n/a	n/a
5	ARID3A	chr6:68597363-68597629	K562	blood:	n/a	n/a
6	ARID3A	chr6:68585707-68586266	K562	blood:	n/a	n/a
7	ARID3A	chr6:68588859-68589349	K562	blood:	n/a	n/a
8	ARID3A	chr6:68587287-68587821	K562	blood:	n/a	n/a
9	ARID3A	chr6:68598616-68600400	K562	blood:	n/a	n/a
10	ATF1	chr6:68608783-68609230	K562	blood:	n/a	n/a
11	ATF1	chr6:68590947-68591336	K562	blood:	n/a	n/a
12	ATF1	chr6:68598554-68599440	K562	blood:	n/a	n/a
13	ATF1	chr6:68592444-68592941	K562	blood:	n/a	n/a
14	ATF1	chr6:68576431-68576606	K562	blood:	n/a	n/a
15	ATF1	chr6:68606467-68606690	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	chr6:68588913-68589303	K562	blood:	n/a	n/a
19	BACH1	chr6:68606755-68606885	K562	blood:	n/a	n/a
20	BACH1	chr6:68585758-68586506	K562	blood:	n/a	n/a
21	BACH1	chr6:68598800-68599114	K562	blood:	n/a	n/a
22	BACH1	chr6:68585892-68586249	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL3	chr6:68591148-68591620	K562	blood:	n/a	n/a
24	BCL3	chr6:68590214-68590374	K562	blood:	n/a	n/a
25	BCL3	chr6:68598839-68599484	K562	blood:	n/a	n/a
26	BCL3	chr6:68588561-68589454	K562	blood:	n/a	n/a
27	BCL3	chr6:68590567-68590728	K562	blood:	n/a	n/a
28	BCL3	chr6:68590634-68591815	K562	blood:	n/a	n/a
29	BCL3	chr6:68590756-68591131	K562	blood:	n/a	n/a
30	BCLAF1	chr6:68590647-68592475	K562	blood:	n/a	n/a
31	BCLAF1	chr6:68596665-68599377	K562	blood:	n/a	n/a
32	BCLAF1	chr6:68590734-68592419	K562	blood:	n/a	n/a
33	BCLAF1	chr6:68597199-68599447	K562	blood:	n/a	n/a
34	BCLAF1	chr6:68594905-68596425	K562	blood:	n/a	n/a
35	BCLAF1	chr6:68594048-68594775	K562	blood:	n/a	n/a
36	BHLHE40	chr6:68595340-68595613	K562	blood:	n/a	n/a
37	BHLHE40	chr6:68590943-68591320	K562	blood:	n/a	n/a
38	BHLHE40	chr6:68591700-68592029	K562	blood:	n/a	n/a
39	BHLHE40	chr6:68607929-68608540	K562	blood:	n/a	n/a
40	BHLHE40	chr6:68597358-68599424	K562	blood:	n/a	n/a
41	CBX3	chr6:68590808-68591319	K562	blood:	n/a	n/a
42	CBX3	chr6:68606363-68606676	K562	blood:	n/a	n/a
43	CBX3	chr6:68549756-68550082	K562	blood:	n/a	n/a
44	CBX3	chr6:68598810-68599526	K562	blood:	n/a	n/a
45	CBX3	chr6:68598539-68599422	K562	blood:	n/a	n/a
46	CBX3	chr6:68614620-68615055	K562	blood:	n/a	n/a
47	CBX3	chr6:68597615-68598167	K562	blood:	n/a	n/a
48	CBX3	chr6:68549722-68550040	K562	blood:	n/a	n/a
49	CBX3	chr6:68566562-68566946	K562	blood:	n/a	n/a
50	CBX3	chr6:68608679-68609139	K562	blood:	n/a	n/a

(count:1406 , 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	NH-A	brain:	n/a
2	chr6:68596739-68596789	NT2-D1	testis:	n/a
3	chr6:68595425-68595475	AG09309	skin:	n/a
4	chr6:68597028-68597078	NH-A	brain:	n/a
5	chr6:68596739-68596789	NT2-D1	testis:	n/a
6	chr6:68595425-68595475	AG09309	skin:	n/a
7	chr6:68595814-68595864	GM12891	blood:	n/a
8	chr6:68595789-68595839	A549	lung:	n/a
9	chr6:68598642-68598692	NHDF-neo	bronchial:	n/a
10	chr6:68596739-68596789	SK-N-MC	brain:	n/a
11	chr6:68595789-68595839	GM12892	blood:	n/a
12	chr6:68596880-68596930	AG09309	skin:	n/a
13	chr6:68598642-68598692	NT2-D1	testis:	n/a
14	chr6:68597649-68597699	U87	brain:	n/a
15	chr6:68599196-68599246	PANC-1	pancreas:	n/a
16	chr6:68596851-68596901	GM19239	blood:	n/a
17	chr6:68597649-68597699	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:68596644-68596694	HRCEpiC	kidney:	n/a
19	chr6:68597649-68597699	IMR90	lung:	fetal
20	chr6:68596851-68596901	PANC-1	pancreas:	n/a
21	chr6:68596887-68596937	MCF-7	breast:	n/a
22	chr6:68599129-68599179	SAEC	small airway:	n/a
23	chr6:68598790-68598840	CMK	blood:	n/a
24	chr6:68596945-68596995	HMEC	breast:	n/a
25	chr6:68597705-68597755	GM12891	blood:	n/a
26	chr6:68599280-68599330	AG10803	skin:	n/a
27	chr6:68595547-68595597	PFSK-1	brain:	n/a
28	chr6:68595425-68595475	HCPEpiC	choroid plexus:	n/a
29	chr6:68599280-68599330	GM12891	blood:	n/a
30	chr6:68596851-68596901	HEK293	kidney:	embryo
31	chr6:68598790-68598840	HRPEpiC	eye:	n/a
32	chr6:68598642-68598692	GM12878	blood:	n/a
33	chr6:68596920-68596970	Hepatocyte	liver:	n/a
34	chr6:68596644-68596694	IMR90	lung:	fetal
35	chr6:68596945-68596995	HAEpiC	amniotic membrane:	n/a
36	chr6:68597028-68597078	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:68599196-68599246	CMK	blood:	n/a
38	chr6:68598790-68598840	ProgFib	skin:	n/a
39	chr6:68598701-68598751	GM06990	blood:	n/a
40	chr6:68599358-68599408	AG09319	gingival:	n/a
41	chr6:68596920-68596970	HepG2	liver:	n/a
42	chr6:68597028-68597078	AoSMC	blood vessel:	n/a
43	chr6:68599196-68599246	HL-60	blood:	n/a
44	chr6:68596920-68596970	AG04449	skin:	fetal
45	chr6:68597028-68597078	ProgFib	skin:	n/a
46	chr6:68597705-68597755	SKMC	muscle:	n/a
47	chr6:68596880-68596930	SK-N-MC	brain:	n/a
48	chr6:68595547-68595597	CMK	blood:	n/a
49	chr6:68597705-68597755	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:68599129-68599179	HPAEpiC	pulmonary alveolar:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:68596719..68599116-chr6:68697886..68700218,3	K562	blood:
2	chr6:68591392..68593317-chr6:68835997..68837691,2	K562	blood:
3	chr6:68596707..68598559-chr6:68885948..68889020,3	K562	blood:
4	chr6:68597158..68599225-chr6:68614213..68617190,2	K562	blood:
5	chr6:68403017..68405900-chr6:68588028..68590720,2	K562	blood:
6	chr6:68591540..68594033-chr6:68744655..68747114,2	K562	blood:
7	chr6:68592130..68593686-chr9:94838364..94839871,2	K562	blood:
8	chr6:68606092..68608064-chr6:68618908..68621057,2	K562	blood:
9	chr6:68540202..68542998-chr6:68546764..68550157,3	K562	blood:
10	chr6:68642346..68643318-chr6:68935421..68936071,2	MCF-7	breast:
11	chr6:68592315..68594490-chr6:68729157..68731583,2	K562	blood:
12	chr6:68580821..68583370-chr6:68587245..68588979,2	K562	blood:
13	chr6:68599985..68602713-chr6:68605698..68607333,2	MCF-7	breast:
14	chr6:68546534..68549959-chr6:68591405..68594115,3	K562	blood:
15	chr6:68546534..68549959-chr6:68591405..68594115,3	K562	blood:
16	chr6:68571846..68575776-chr6:68585340..68589247,5	K562	blood:
17	chr6:68568907..68571616-chr6:68584376..68587253,2	K562	blood:
18	chr6:68596440..68599032-chr6:68647248..68649168,3	K562	blood:
19	chr6:68589435..68592511-chr6:68936619..68941410,4	K562	blood:
20	chr6:68590010..68592116-chr6:68758239..68761217,2	K562	blood:
21	chr6:68412434..68414327-chr6:68587582..68589254,2	K562	blood:
22	chr6:68595612..68597552-chr6:68616744..68619642,2	K562	blood:
23	chr6:68595949..68597859-chr6:68734333..68736391,3	K562	blood:
24	chr6:68487636..68489959-chr6:68585344..68587572,2	K562	blood:
25	chr6:68592573..68603518-chr6:68604068..68612413,29	K562	blood:
26	chr6:68604107..68606709-chr6:68609617..68614181,4	K562	blood:
27	chr6:68506908..68510214-chr6:68588930..68590665,3	K562	blood:
28	chr6:68593774..68595835-chr6:68943897..68947286,3	K562	blood:
29	chr6:68596140..68598013-chr6:68631347..68633345,2	K562	blood:
30	chr6:68604720..68607895-chr6:68608418..68610279,3	K562	blood:
31	chr6:68597467..68600079-chr6:68619795..68621938,2	K562	blood:
32	chr6:68564294..68566367-chr6:68570127..68572578,2	MCF-7	breast:
33	chr6:68547547..68550357-chr6:68551915..68554138,2	K562	blood:
34	chr6:68569432..68571622-chr6:68584062..68586266,2	K562	blood:
35	chr6:68597581..68600256-chr6:68643014..68644581,2	K562	blood:
36	chr6:68607711..68610466-chr6:68621509..68623559,2	K562	blood:
37	chr6:68573446..68581402-chr6:68582909..68592336,10	K562	blood:
38	chr6:68596857..68599140-chr6:68728462..68730738,2	K562	blood:
39	chr6:68595545..68597855-chr6:68811706..68813567,2	K562	blood:
40	chr6:68310865..68312507-chr6:68587249..68589737,2	K562	blood:
41	chr6:68536915..68539495-chr6:68589360..68592356,2	K562	blood:
42	chr6:68596878..68598658-chr6:68612874..68615713,2	K562	blood:
43	chr6:68591172..68594136-chr6:68947672..68950423,2	K562	blood:
44	chr6:68590326..68593646-chr6:68740813..68742652,3	K562	blood:
45	chr6:68590714..68592952-chr6:68747177..68749735,2	K562	blood:
46	chr6:68586431..68588807-chr6:68750626..68752496,2	K562	blood:
47	chr6:68596476..68598513-chr6:70873784..70875846,2	K562	blood:
48	chr6:67796143..67796843-chr6:68573181..68573682,2	MCF-7	breast:
49	chr6:68562527..68565215-chr6:68588017..68590595,2	K562	blood:
50	chr6:68596878..68598658-chr6:68612874..68615713,2	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
ENSG00000270509	TF binding region
ENSG00000227706	TF binding region
ENSG00000270509	CpG island
ENSG00000227706	CpG island
ENSG00000270509	chromatin interactions
ENSG00000227706	chromatin interactions

Extended variants
information (count: 2110 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2110 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16880598	chr6:68545302-68545303	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375850533	chr6:68545343-68545344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569957332	chr6:68545382-68545383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116530969	chr6:68545386-68545387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556611742	chr6:68549210-68549211	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs574957272	chr6:68549226-68549227	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs546239675	chr6:68549239-68549240	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs5877111	chr6:68549248-68549249	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs559750774	chr6:68549252-68549253	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs79129047	chr6:68549275-68549276	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs542400185	chr6:68549295-68549296	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs182799139	chr6:68549355-68549356	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs554451097	chr6:68549396-68549397	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs577067960	chr6:68549407-68549408	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs531211182	chr6:68549417-68549418	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs187078142	chr6:68549419-68549420	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs573032079	chr6:68549420-68549421	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs149293890	chr6:68549443-68549444	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs540155556	chr6:68549461-68549462	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs1399224	chr6:68549473-68549474	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs546199370	chr6:68549483-68549484	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs185131527	chr6:68556657-68556658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541837677	chr6:68556691-68556692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535411926	chr6:68556702-68556703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531483837	chr6:68556751-68556752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142725801	chr6:68556758-68556759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553712823	chr6:68556788-68556789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527630742	chr6:68556793-68556794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543442920	chr6:68556838-68556839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201156759	chr6:68556865-68556866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566892522	chr6:68556932-68556933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150721041	chr6:68556937-68556938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530601711	chr6:68556992-68556993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs72888198	chr6:68557008-68557009	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs138999672	chr6:68557037-68557038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539534472	chr6:68557050-68557051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538041464	chr6:68557077-68557078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373774245	chr6:68557083-68557084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190332442	chr6:68557084-68557085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs578172700	chr6:68557101-68557102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540959646	chr6:68557108-68557109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34685474	chr6:68557117-68557118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs149436729	chr6:68557120-68557121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542645162	chr6:68557128-68557129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566641467	chr6:68557175-68557176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531472305	chr6:68557213-68557214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144828112	chr6:68557273-68557274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13216053	chr6:68557289-68557290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs368290918	chr6:68557302-68557303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556902542	chr6:68557309-68557310	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:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:68543600-68545400	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr6:68549200-68549600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
3	chr6:68556600-68559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:68557800-68558200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:68563800-68564200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:68564000-68564400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:68581600-68586200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:68583800-68584000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:68585800-68586200	Enhancers	Adipose Nuclei	Adipose
10	chr6:68585800-68589400	Enhancers	K562	blood
11	chr6:68587400-68588000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:68588200-68588600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:68588600-68589000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:68589000-68589200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:68589200-68591200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:68589400-68590800	Weak transcription	K562	blood
17	chr6:68590800-68591000	ZNF genes & repeats	K562	blood
18	chr6:68591000-68591600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:68591000-68591600	Enhancers	Hela-S3	cervix
20	chr6:68591000-68591800	Enhancers	NH-A	brain
21	chr6:68591000-68598400	Transcr. at gene 5' and 3'	K562	blood
22	chr6:68591200-68592000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:68591400-68596800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:68591600-68591800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:68591800-68595000	Weak transcription	NH-A	brain
26	chr6:68592000-68596600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:68595000-68595600	Active TSS	Primary T killer memory cells from peripheral blood	blood
28	chr6:68598200-68599000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:68598400-68598800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
30	chr6:68598400-68601400	Active TSS	K562	blood
31	chr6:68598600-68599200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:68598800-68599200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:68598800-68599600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr6:68598800-68599800	Enhancers	Hela-S3	cervix
35	chr6:68598800-68600200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:68599000-68599200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr6:68599200-68599800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:68599600-68607800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr6:68599800-68600200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:68600000-68601400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr6:68600200-68600600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr6:68600400-68601400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:68600600-68601200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr6:68600600-68601200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr6:68600800-68601400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr6:68601000-68601400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr6:68601400-68601600	Weak transcription	K562	blood
48	chr6:68601600-68602000	ZNF genes & repeats	K562	blood
49	chr6:68602000-68604800	Weak transcription	K562	blood
50	chr6:68604800-68605200	Genic enhancers	K562	blood

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