Variant report

Variant	nsv1025290
Chromosome Location	chr6:62236498-62913561
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	chr6:62518943-62519292	HepG2	liver:	n/a	n/a
2	BACH1	chr6:62291135-62291160	K562	blood:	n/a	n/a
3	BACH1	chr6:62328176-62328215	K562	blood:	n/a	n/a
4	BACH1	chr6:62501051-62501180	K562	blood:	n/a	n/a
5	BACH1	chr6:62236939-62236976	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr6:62283970-62284243	GM12878	blood:	n/a	n/a
7	BATF	chr6:62248776-62249065	GM12878	blood:	n/a	n/a
8	BATF	chr6:62283972-62284263	GM12878	blood:	n/a	n/a
9	BATF	chr6:62248793-62249038	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:62283933-62284208	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:62283978-62284284	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:62283930-62284249	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:62469628-62469639	HepG2	liver:	n/a	n/a
14	BRCA1	chr6:62447601-62447670	GM12878	blood:	n/a	n/a
15	CBX3	chr6:62667309-62667485	K562	blood:	n/a	n/a
16	CEBPB	chr6:62366774-62367019	A549	lung:	n/a	chr6:62366900-62366911 chr6:62366838-62366849
17	CEBPB	chr6:62415914-62416204	HepG2	liver:	n/a	chr6:62416044-62416055
18	CEBPB	chr6:62514108-62514295	HepG2	liver:	n/a	chr6:62514202-62514213
19	CEBPB	chr6:62380798-62381027	A549	lung:	n/a	chr6:62380966-62380977
20	CEBPB	chr6:62766627-62766891	HepG2	liver:	n/a	chr6:62766803-62766816
21	CEBPB	chr6:62465708-62466033	H1-hESC	embryonic stem cell:	n/a	chr6:62465871-62465882
22	CEBPB	chr6:62371143-62371454	HepG2	liver:	n/a	chr6:62371302-62371313 chr6:62371303-62371312 chr6:62371303-62371312 chr6:62371303-62371312 chr6:62371301-62371312 chr6:62371303-62371312
23	CEBPB	chr6:62465746-62466038	HepG2	liver:	n/a	chr6:62465871-62465882
24	CEBPB	chr6:62755432-62755741	K562	blood:	n/a	chr6:62755597-62755610 chr6:62755599-62755608 chr6:62755597-62755608 chr6:62755599-62755608 chr6:62755599-62755608 chr6:62755597-62755610 chr6:62755599-62755608 chr6:62755599-62755610
25	CEBPB	chr6:62648989-62649189	HepG2	liver:	n/a	chr6:62649068-62649079
26	CEBPB	chr6:62859698-62860257	H1-hESC	embryonic stem cell:	n/a	chr6:62859994-62860002 chr6:62860076-62860093
27	CEBPB	chr6:62859944-62860242	IMR90	lung:	n/a	chr6:62859994-62860002 chr6:62860076-62860093
28	CEBPB	chr6:62650178-62650520	HepG2	liver:	n/a	chr6:62650355-62650366
29	CEBPB	chr6:62859893-62860267	HepG2	liver:	n/a	chr6:62859994-62860002 chr6:62860076-62860093
30	CEBPB	chr6:62859917-62860272	Hela-S3	cervix:	n/a	chr6:62859994-62860002 chr6:62860076-62860093
31	CEBPB	chr6:62684043-62684372	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:62375156-62375272	H1-hESC	embryonic stem cell:	n/a	chr6:62375214-62375227
33	CEBPB	chr6:62315823-62315926	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:62766634-62766936	A549	lung:	n/a	chr6:62766803-62766816
35	CEBPB	chr6:62465764-62466017	MCF-7	breast:	n/a	chr6:62465871-62465882
36	CEBPB	chr6:62380787-62381078	HepG2	liver:	n/a	chr6:62380966-62380977
37	CEBPB	chr6:62672094-62672306	H1-hESC	embryonic stem cell:	n/a	chr6:62672222-62672233
38	CEBPB	chr6:62859948-62860309	MCF-7	breast:	n/a	chr6:62859994-62860002 chr6:62860076-62860093
39	CEBPB	chr6:62860002-62860254	A549	lung:	n/a	chr6:62860076-62860093
40	CEBPB	chr6:62514837-62515000	HepG2	liver:	n/a	chr6:62514913-62514924
41	CEBPB	chr6:62645680-62645924	HepG2	liver:	n/a	chr6:62645793-62645804
42	CEBPB	chr6:62690606-62690741	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:62366757-62367062	HepG2	liver:	n/a	chr6:62366900-62366911 chr6:62366838-62366849
44	CEBPB	chr6:62645621-62645879	IMR90	lung:	n/a	chr6:62645793-62645804
45	CEBPB	chr6:62672054-62672375	HepG2	liver:	n/a	chr6:62672222-62672233
46	CEBPB	chr6:62621793-62622001	HepG2	liver:	n/a	chr6:62621876-62621889 chr6:62621876-62621887
47	CEBPB	chr6:62765520-62765855	HepG2	liver:	n/a	chr6:62765683-62765694
48	CEBPB	chr6:62868080-62868229	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr6:62753663-62753711	HepG2	liver:	n/a	chr6:62753684-62753695
50	CEBPB	chr6:62603739-62604059	HepG2	liver:	n/a	chr6:62603873-62603884 chr6:62603871-62603882 chr6:62603871-62603884

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:62737607-62737657	HL-60	blood:	n/a
2	chr6:62737607-62737657	HL-60	blood:	n/a
3	chr6:62284299-62284349	ECC-1	luminal epithelium:	n/a
4	chr6:62737607-62737657	RPTEC	kidney:	n/a
5	chr6:62737607-62737657	NT2-D1	testis:	n/a
6	chr6:62596341-62596391	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:62737607-62737657	SK-N-SH	brain:	n/a
8	chr6:62596341-62596391	SK-N-SH_RA	brain:	n/a
9	chr6:62642433-62642483	ECC-1	luminal epithelium:	n/a
10	chr6:62642433-62642483	MCF-7	breast:	n/a
11	chr6:62737607-62737657	PFSK-1	brain:	n/a
12	chr6:62737607-62737657	HEEpiC	esophagus:	n/a
13	chr6:62284299-62284349	Jurkat	blood:	n/a
14	chr6:62596341-62596391	HUVEC	blood vessel:	n/a
15	chr6:62642433-62642483	SAEC	small airway:	n/a
16	chr6:62737607-62737657	H1-hESC	embryonic stem cell:	embryo
17	chr6:62596341-62596391	HEK293	kidney:	embryo
18	chr6:62284299-62284349	NHBE	bronchial:	n/a
19	chr6:62642433-62642483	HNPCEpiC	eye:	n/a
20	chr6:62596341-62596391	SK-N-SH	brain:	n/a
21	chr6:62642433-62642483	ovcar-3	ovarian:	n/a
22	chr6:62737607-62737657	LNCaP	prostate:	n/a
23	chr6:62642433-62642483	LNCaP	prostate:	n/a
24	chr6:62737607-62737657	T-47D	breast:	n/a
25	chr6:62737607-62737657	AG04449	skin:	fetal
26	chr6:62642433-62642483	PrEC	prostate:	n/a
27	chr6:62284299-62284349	HRCEpiC	kidney:	n/a
28	chr6:62737607-62737657	Caco-2	colon:	n/a
29	chr6:62737607-62737657	HCF	heart:	n/a
30	chr6:62596341-62596391	NT2-D1	testis:	n/a
31	chr6:62642433-62642483	AG09309	skin:	n/a
32	chr6:62284299-62284349	HRPEpiC	eye:	n/a
33	chr6:62642433-62642483	SK-N-MC	brain:	n/a
34	chr6:62642433-62642483	HCPEpiC	choroid plexus:	n/a
35	chr6:62284299-62284349	GM12892	blood:	n/a
36	chr6:62596341-62596391	HCM	heart:	n/a
37	chr6:62642433-62642483	GM12891	blood:	n/a
38	chr6:62737607-62737657	SKMC	muscle:	n/a
39	chr6:62642433-62642483	SK-N-SH_RA	brain:	n/a
40	chr6:62284299-62284349	LNCaP	prostate:	n/a
41	chr6:62737607-62737657	AoSMC	blood vessel:	n/a
42	chr6:62642433-62642483	HRCEpiC	kidney:	n/a
43	chr6:62596341-62596391	U87	brain:	n/a
44	chr6:62737607-62737657	ECC-1	luminal epithelium:	n/a
45	chr6:62642433-62642483	RPTEC	kidney:	n/a
46	chr6:62596341-62596391	AG09319	gingival:	n/a
47	chr6:62596341-62596391	HMEC	breast:	n/a
48	chr6:62642433-62642483	A549	lung:	n/a
49	chr6:62737607-62737657	HCT-116	colon:	n/a
50	chr6:62596341-62596391	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:62519001..62519629-chr6:62859955..62860555,3	MCF-7	breast:
2	chr6:62852057..62854070-chr6:62855241..62858140,2	MCF-7	breast:
3	chr6:62852057..62854070-chr6:62855241..62858140,2	MCF-7	breast:
4	chr6:62520772..62522597-chr6:62523953..62526303,2	K562	blood:
5	chr6:57445367..57446031-chr6:62860058..62860574,2	MCF-7	breast:
6	chr4:164676002..164676634-chr6:62381037..62381706,2	MCF-7	breast:
7	chr6:57766644..57767228-chr6:62859661..62860581,2	MCF-7	breast:
8	chr6:62338455..62341416-chr6:62349346..62350925,2	K562	blood:
9	chr6:62761124..62761875-chrX:154244873..154245663,2	MCF-7	breast:
10	chr1:109802150..109805070-chr6:62296846..62299543,2	MCF-7	breast:
11	chr6:62519001..62519629-chr6:62859955..62860555,3	MCF-7	breast:
12	chr6:62545749..62547961-chr6:62548535..62550868,2	MCF-7	breast:
13	chr6:62621722..62623294-chr6:62626600..62628744,2	MCF-7	breast:
14	chr6:62338455..62341416-chr6:62349346..62350925,2	K562	blood:
15	chr6:62621722..62623294-chr6:62626600..62628744,2	MCF-7	breast:
16	chr6:62520772..62522597-chr6:62523953..62526303,2	K562	blood:
17	chr3:113873972..113874534-chr6:62859704..62860673,2	MCF-7	breast:
18	chr6:62518763..62519292-chr6:62993656..62994388,2	MCF-7	breast:
19	chr6:62776601..62778161-chr6:62783168..62785146,2	K562	blood:
20	chr6:62776601..62778161-chr6:62783168..62785146,2	K562	blood:
21	chr6:62518549..62519303-chr6:63600674..63601315,2	MCF-7	breast:
22	chr20:45985491..45988318-chr6:62588370..62590548,2	MCF-7	breast:
23	chr6:62545749..62547961-chr6:62548535..62550868,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KHDRBS2-1	chr6:62362159-62362222	NONHSAT113330
2	lnc-KHDRBS2-1	chr6:62369022-62369055	XLOC_005755
3	lnc-KHDRBS2-1	chr6:62371187-62371274	XLOC_005755
4	lnc-KHDRBS2-1	chr6:62340207-62340406	XLOC_005755
5	lnc-KHDRBS2-1	chr6:62362160-62362222	XLOC_005755
6	lnc-KHDRBS2-1	chr6:62371186-62371274	NONHSAT113330
7	lnc-KHDRBS2-1	chr6:62369021-62369055	NONHSAT113330
8	lnc-KHDRBS2-1	chr6:62340206-62340406	NONHSAT113330

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KHDRBS2	hsa-miR-335-5p	chr6:62390601-62390623

Variant related genes	Relation type
ENSG00000250686	TF binding region
MTRNR2L9	TF binding region
ENSG00000250686	CpG island
MTRNR2L9	CpG island
ENSG00000101040	chromatin interactions

Extended variants
information (count: 18281 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:18281 , 50 per page) page: 1 2 3 4 5 6 7 ... 366

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535570379	chr6:62248203-62248204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558746541	chr6:62248210-62248211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577115560	chr6:62248239-62248240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73757584	chr6:62248262-62248263	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs138366125	chr6:62248264-62248265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182578758	chr6:62248265-62248266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556516038	chr6:62248307-62248308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149514052	chr6:62248333-62248334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144073263	chr6:62248407-62248408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs78185469	chr6:62248408-62248409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148658712	chr6:62248409-62248410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187239617	chr6:62248436-62248437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191273281	chr6:62248443-62248444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551760558	chr6:62248444-62248445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182597519	chr6:62248487-62248488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550413443	chr6:62248490-62248491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567244693	chr6:62248529-62248530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377367400	chr6:62248586-62248587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189031342	chr6:62248592-62248593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374869357	chr6:62248615-62248616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11754795	chr6:62248621-62248622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193138697	chr6:62248693-62248694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546554678	chr6:62248729-62248730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568294279	chr6:62248758-62248759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535663952	chr6:62248778-62248779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557167232	chr6:62248789-62248790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185230877	chr6:62248795-62248796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575417073	chr6:62248797-62248798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs62424580	chr6:62248820-62248821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189054344	chr6:62248847-62248848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557774527	chr6:62248874-62248875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35515981	chr6:62248884-62248885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572747373	chr6:62248907-62248908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs9454533	chr6:62248920-62248921	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs192192366	chr6:62248959-62248960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141386733	chr6:62248962-62248963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1414816	chr6:62248985-62248986	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs562699543	chr6:62248987-62248988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533288643	chr6:62248996-62248997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535919837	chr6:62265805-62265806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139528755	chr6:62265827-62265828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186403631	chr6:62265828-62265829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144185699	chr6:62265829-62265830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565856050	chr6:62265838-62265839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536017692	chr6:62265887-62265888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190872595	chr6:62265897-62265898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566636734	chr6:62265900-62265901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569739871	chr6:62265908-62265909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73476807	chr6:62265913-62265914	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs374612576	chr6:62265914-62265915	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Lung cancer	19547694	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Medulloblastoma	21163964	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:62248200-62249000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:62265800-62266200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:62266000-62266200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:62266000-62266200	ZNF genes & repeats	Pancreas	Pancrea
5	chr6:62272600-62274600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
6	chr6:62273000-62274200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr6:62273200-62273400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
8	chr6:62273200-62273400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
9	chr6:62273600-62274000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:62273600-62274000	Enhancers	Liver	Liver
11	chr6:62273800-62274600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr6:62274200-62274400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:62278800-62284600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr6:62284600-62284800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:62284600-62284800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
16	chr6:62284600-62284800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
17	chr6:62284600-62284800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
18	chr6:62284600-62284800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:62284600-62284800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
20	chr6:62284600-62284800	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr6:62284600-62284800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
22	chr6:62284600-62284800	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr6:62284600-62284800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:62284600-62284800	ZNF genes & repeats	Adipose Nuclei	Adipose
25	chr6:62284600-62284800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr6:62284600-62284800	ZNF genes & repeats	Colon Smooth Muscle	Colon
27	chr6:62284600-62284800	Enhancers	Fetal Heart	heart
28	chr6:62284600-62284800	ZNF genes & repeats	Pancreas	Pancrea
29	chr6:62284800-62285600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:62288600-62289400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:62289400-62294200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:62291000-62291200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr6:62291200-62292400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:62294200-62297800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr6:62295200-62296400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:62296400-62298000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr6:62301400-62302000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr6:62301400-62302000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr6:62301400-62302000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr6:62301400-62302400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr6:62301400-62303000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:62301400-62303000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:62301600-62303200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:62301800-62302200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr6:62301800-62302600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr6:62301800-62303200	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr6:62302000-62302600	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr6:62302000-62302800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr6:62302000-62310600	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr6:62302400-62303600	Weak transcription	H9 Cell Line	embryonic stem cell

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