Variant report

Variant	nsv1016430
Chromosome Location	chr6:147662541-147711882
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:449)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:449 , 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	chr6:147704126-147704442	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:147704152-147704396	K562	blood:	n/a	n/a
3	BACH1	chr6:147668403-147668878	K562	blood:	n/a	n/a
4	BACH1	chr6:147700286-147700486	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:147689088-147689285	K562	blood:	n/a	n/a
6	BACH1	chr6:147691714-147691717	K562	blood:	n/a	n/a
7	BATF	chr6:147706532-147706728	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:147706516-147706817	GM12878	blood:	n/a	n/a
9	BCL3	chr6:147666121-147666736	K562	blood:	n/a	n/a
10	BCL3	chr6:147673487-147674459	K562	blood:	n/a	n/a
11	BCL3	chr6:147666819-147668873	K562	blood:	n/a	n/a
12	BHLHE40	chr6:147705956-147706203	GM12878	blood:	n/a	n/a
13	CCNT2	chr6:147667511-147667654	K562	blood:	n/a	n/a
14	CCNT2	chr6:147706073-147706272	K562	blood:	n/a	n/a
15	CCNT2	chr6:147670514-147670836	K562	blood:	n/a	n/a
16	CCNT2	chr6:147667909-147668231	K562	blood:	n/a	n/a
17	CEBPB	chr6:147709347-147709658	HepG2	liver:	n/a	chr6:147709498-147709509
18	CEBPB	chr6:147709435-147709556	IMR90	lung:	n/a	chr6:147709498-147709509
19	CEBPB	chr6:147693227-147693415	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:147704218-147704319	K562	blood:	n/a	chr6:147704246-147704255
21	CEBPB	chr6:147700229-147700250	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:147693276-147693410	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:147709352-147709655	K562	blood:	n/a	chr6:147709498-147709509
24	CHD2	chr6:147667441-147667450	K562	blood:	n/a	n/a
25	CHD2	chr6:147700134-147700318	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr6:147704140-147704290	GM12865	blood:	n/a	chr6:147704275-147704284 chr6:147704272-147704290
27	CTCF	chr6:147704160-147704310	MCF-7	breast:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
28	CTCF	chr6:147704220-147704370	HCT-116	colon:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
29	CTCF	chr6:147704240-147704390	HAc	cerebellar:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
30	CTCF	chr6:147704206-147704343	LNCaP	prostate:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
31	CTCF	chr6:147687580-147687730	HepG2	liver:	n/a	n/a
32	CTCF	chr6:147704220-147704319	Lung_OC	lung:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
33	CTCF	chr6:147704160-147704310	Caco-2	colon:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
34	CTCF	chr6:147687500-147687650	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr6:147704088-147704438	GM12878	blood:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
36	CTCF	chr6:147704140-147704290	HepG2	liver:	n/a	chr6:147704275-147704284 chr6:147704272-147704290
37	CTCF	chr6:147704155-147704378	Pancreas_OC	pancreas:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
38	CTCF	chr6:147704086-147704425	H1-hESC	embryonic stem cell:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
39	CTCF	chr6:147704120-147704270	HCT-116	colon:	n/a	n/a
40	CTCF	chr6:147704137-147704409	HUVEC	blood vessel:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
41	CTCF	chr6:147704160-147704310	HMEC	breast:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
42	CTCF	chr6:147704200-147704350	GM12874	blood:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
43	CTCF	chr6:147687449-147687775	GM12878	blood:	n/a	n/a
44	CTCF	chr6:147704160-147704310	NHDF-neo	bronchial:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
45	CTCF	chr6:147703939-147704019	K562	blood:	n/a	n/a
46	CTCF	chr6:147704680-147704830	HVMF	connective:	n/a	chr6:147704788-147704795
47	CTCF	chr6:147687520-147687670	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr6:147703958-147704011	Gliobla	brain:	n/a	n/a
49	CTCF	chr6:147704184-147704328	GM12878	blood:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290
50	CTCF	chr6:147704220-147704370	AoAF	blood vessel:	n/a	chr6:147704275-147704284 chr6:147704274-147704295 chr6:147704272-147704290

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:147705971-147706021	HRCEpiC	kidney:	n/a
2	chr6:147705971-147706021	U87	brain:	n/a
3	chr6:147705971-147706021	HepG2	liver:	n/a
4	chr6:147705971-147706021	SK-N-MC	brain:	n/a
5	chr6:147705971-147706021	SK-N-SH	brain:	n/a
6	chr6:147705971-147706021	HEK293	kidney:	embryo
7	chr6:147705971-147706021	HEEpiC	esophagus:	n/a
8	chr6:147705971-147706021	GM06990	blood:	n/a
9	chr6:147705971-147706021	NT2-D1	testis:	n/a
10	chr6:147705971-147706021	LNCaP	prostate:	n/a
11	chr6:147705971-147706021	MCF-7	breast:	n/a
12	chr6:147705971-147706021	PrEC	prostate:	n/a
13	chr6:147705971-147706021	H1-hESC	embryonic stem cell:	embryo
14	chr6:147705971-147706021	HL-60	blood:	n/a
15	chr6:147705971-147706021	Hepatocyte	liver:	n/a
16	chr6:147705971-147706021	HCPEpiC	choroid plexus:	n/a
17	chr6:147705971-147706021	BJ	skin:	n/a
18	chr6:147705971-147706021	ovcar-3	ovarian:	n/a
19	chr6:147705971-147706021	HCT-116	colon:	n/a
20	chr6:147705971-147706021	HCM	heart:	n/a
21	chr6:147705971-147706021	Jurkat	blood:	n/a
22	chr6:147705971-147706021	AoSMC	blood vessel:	n/a
23	chr6:147705971-147706021	HNPCEpiC	eye:	n/a
24	chr6:147705971-147706021	SK-N-SH_RA	brain:	n/a
25	chr6:147705971-147706021	CMK	blood:	n/a
26	chr6:147705971-147706021	NHDF-neo	bronchial:	n/a
27	chr6:147705971-147706021	SAEC	small airway:	n/a
28	chr6:147705971-147706021	AG10803	skin:	n/a
29	chr6:147705971-147706021	HAEpiC	amniotic membrane:	n/a
30	chr6:147705971-147706021	AG04450	lung:	fetal
31	chr6:147705971-147706021	GM19239	blood:	n/a
32	chr6:147705971-147706021	AG09319	gingival:	n/a
33	chr6:147705971-147706021	AG09309	skin:	n/a
34	chr6:147705971-147706021	Hela-S3	cervix:	n/a
35	chr6:147705971-147706021	PFSK-1	brain:	n/a
36	chr6:147705971-147706021	HCF	heart:	n/a
37	chr6:147705971-147706021	HMEC	breast:	n/a
38	chr6:147705971-147706021	Caco-2	colon:	n/a
39	chr6:147705971-147706021	PANC-1	pancreas:	n/a
40	chr6:147705971-147706021	IMR90	lung:	fetal
41	chr6:147705971-147706021	GM12892	blood:	n/a
42	chr6:147705971-147706021	GM12878	blood:	n/a
43	chr6:147705971-147706021	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:147705971-147706021	HIPEpiC	eye:	n/a
45	chr6:147705971-147706021	NH-A	brain:	n/a
46	chr6:147705971-147706021	AG04449	skin:	fetal
47	chr6:147705971-147706021	ECC-1	luminal epithelium:	n/a
48	chr6:147705971-147706021	SKMC	muscle:	n/a
49	chr6:147705971-147706021	T-47D	breast:	n/a
50	chr6:147705971-147706021	NHBE	bronchial:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:147590566..147593187-chr6:147668783..147670491,2	K562	blood:
2	chr6:147689765..147692584-chr6:147692811..147694945,3	K562	blood:
3	chr6:147685432..147688337-chr6:147695787..147697611,2	K562	blood:
4	chr6:147603613..147606358-chr6:147670525..147673088,2	K562	blood:
5	chr6:147632716..147635508-chr6:147662008..147664678,2	K562	blood:
6	chr6:147205531..147207061-chr6:147703036..147705763,2	K562	blood:
7	chr6:147660277..147661948-chr6:147667119..147669406,3	K562	blood:
8	chr6:147685644..147688085-chr6:147690225..147693015,3	K562	blood:
9	chr6:147223233..147223931-chr6:147703798..147704743,3	MCF-7	breast:
10	chr6:147690188..147692796-chr6:147704081..147706540,2	K562	blood:
11	chr6:147685432..147688337-chr6:147695787..147697611,2	K562	blood:
12	chr6:147674142..147676430-chr6:147682128..147684419,2	K562	blood:
13	chr6:147689027..147691902-chr6:147709302..147712120,2	K562	blood:
14	chr6:147689027..147691902-chr6:147709302..147712120,2	K562	blood:
15	chr6:147664249..147666005-chr6:147673962..147676762,2	K562	blood:
16	chr6:147178386..147179221-chr6:147703832..147704746,2	K562	blood:
17	chr6:147711855..147712651-chr6:148465819..148466536,2	MCF-7	breast:
18	chr6:147703869..147707372-chr6:147716822..147719564,3	K562	blood:
19	chr6:147674544..147676430-chr6:147682128..147684379,2	K562	blood:
20	chr6:147664249..147666005-chr6:147673962..147676762,2	K562	blood:
21	chr6:147656651..147659258-chr6:147668248..147670413,2	K562	blood:
22	chr6:147691862..147694134-chr6:147695715..147698505,2	K562	blood:
23	chr6:147691862..147694134-chr6:147695715..147698505,2	K562	blood:
24	chr6:147648442..147651274-chr6:147664737..147666741,2	MCF-7	breast:
25	chr6:147689765..147692584-chr6:147692811..147694945,3	K562	blood:
26	chr6:147674142..147676430-chr6:147682128..147684419,2	K562	blood:
27	chr6:147685644..147688085-chr6:147690225..147693015,3	K562	blood:
28	chr6:147223830..147226657-chr6:147694168..147696836,2	K562	blood:
29	chr6:147690188..147692861-chr6:147705040..147707677,2	K562	blood:
30	chr6:147704406..147707731-chr6:147708554..147712454,8	K562	blood:
31	chr6:147703628..147707069-chr6:147708418..147712454,5	K562	blood:
32	chr6:147209785..147211664-chr6:147702919..147705378,2	K562	blood:
33	chr6:147707091..147709713-chr6:147711125..147713701,2	K562	blood:
34	chr6:147710173..147716177-chr6:147716262..147720570,6	K562	blood:
35	chr6:147690188..147692861-chr6:147705040..147707677,2	K562	blood:
36	chr6:147674544..147676430-chr6:147682128..147684379,2	K562	blood:
37	chr6:147690188..147692796-chr6:147704081..147706540,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STXBP5-1	chr6:147708800-147708872	ENSG00000225135
2	lnc-STXBP5-1	chr6:147710198-147711601	ENSG00000225135
3	lnc-STXBP5-3	chr6:147708957-147709300	expReg_chr6_10989_+

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	STXBP5	hsa-miR-21-5p	chr6:147708269-147708290
2	STXBP5	hsa-miR-21-5p	chr6:147706426-147706447

Variant related genes	Relation type
ENSG00000225135	TF binding region
ENSG00000225135	CpG island
ENSG00000225135	chromatin interactions

Extended variants
information (count: 1652 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554235732	chr6:147662541-147662542	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564472746	chr6:147662543-147662544	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564924175	chr6:147662544-147662545	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562000664	chr6:147662546-147662547	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527646399	chr6:147662593-147662594	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182688086	chr6:147662637-147662638	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561585883	chr6:147662695-147662696	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369964231	chr6:147662752-147662753	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373303076	chr6:147662792-147662793	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs36101070	chr6:147662821-147662822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9717954	chr6:147662835-147662836	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528573923	chr6:147662851-147662852	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530268883	chr6:147662886-147662887	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529561458	chr6:147662899-147662900	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149558305	chr6:147662900-147662901	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs62435631	chr6:147662912-147662913	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548735259	chr6:147662921-147662922	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550343494	chr6:147662933-147662934	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568998076	chr6:147663044-147663045	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376224652	chr6:147663119-147663120	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531418934	chr6:147663133-147663134	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139064281	chr6:147663138-147663139	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571284579	chr6:147663149-147663150	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144916679	chr6:147663166-147663167	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553793452	chr6:147663179-147663180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567542752	chr6:147663195-147663196	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536104487	chr6:147663204-147663205	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187003657	chr6:147663223-147663224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191477568	chr6:147663309-147663310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577442733	chr6:147663331-147663332	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183679008	chr6:147663343-147663344	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114011719	chr6:147663361-147663362	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572113769	chr6:147663436-147663437	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190487864	chr6:147663453-147663454	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561470911	chr6:147663461-147663462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147512318	chr6:147663516-147663517	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370644878	chr6:147663585-147663586	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550003189	chr6:147663605-147663606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530394552	chr6:147663671-147663672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117824912	chr6:147663694-147663695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147945603	chr6:147663712-147663713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532724904	chr6:147663721-147663722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551503655	chr6:147663798-147663799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538966794	chr6:147663853-147663854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61078293	chr6:147664002-147664003	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs527337745	chr6:147664087-147664088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141859430	chr6:147664120-147664121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567477225	chr6:147664167-147664168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73787121	chr6:147664195-147664196	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs549776540	chr6:147664202-147664203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147584400-147684600	Weak transcription	Brain Angular Gyrus	brain
2	chr6:147607400-147707400	Weak transcription	Colon Smooth Muscle	Colon
3	chr6:147609800-147667000	Weak transcription	NHEK	skin
4	chr6:147610200-147700200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:147617400-147680200	Weak transcription	Small Intestine	intestine
6	chr6:147619200-147690200	Weak transcription	Fetal Heart	heart
7	chr6:147622600-147708200	Weak transcription	Psoas Muscle	Psoas
8	chr6:147625800-147664600	Weak transcription	Spleen	Spleen
9	chr6:147625800-147667400	Weak transcription	Gastric	stomach
10	chr6:147626000-147687000	Weak transcription	Lung	lung
11	chr6:147626000-147700200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr6:147626200-147662600	Weak transcription	Pancreas	Pancrea
13	chr6:147626200-147670200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:147626200-147684000	Weak transcription	Brain Hippocampus Middle	brain
15	chr6:147626200-147684000	Weak transcription	Fetal Muscle Trunk	muscle
16	chr6:147626200-147687200	Weak transcription	Fetal Muscle Leg	muscle
17	chr6:147626200-147707600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:147626400-147700000	Weak transcription	Brain Germinal Matrix	brain
19	chr6:147628000-147668000	Weak transcription	Aorta	Aorta
20	chr6:147628200-147687000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr6:147631400-147707200	Weak transcription	Hela-S3	cervix
22	chr6:147633800-147684400	Weak transcription	Ovary	ovary
23	chr6:147637000-147686800	Weak transcription	A549	lung
24	chr6:147640000-147664400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr6:147642800-147705000	Weak transcription	HepG2	liver
26	chr6:147643600-147667000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr6:147643800-147680200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr6:147643800-147680200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr6:147643800-147680200	Weak transcription	Thymus	Thymus
30	chr6:147643800-147686800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr6:147644000-147669200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr6:147644200-147704000	Weak transcription	GM12878-XiMat	blood
33	chr6:147644400-147679200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr6:147644400-147686600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr6:147644600-147684400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr6:147644800-147663600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr6:147644800-147683600	Weak transcription	Fetal Brain Female	brain
38	chr6:147645200-147682000	Weak transcription	HMEC	breast
39	chr6:147645200-147715000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr6:147645800-147685000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:147649000-147687200	Weak transcription	Right Ventricle	heart
42	chr6:147649000-147705000	Weak transcription	Fetal Brain Male	brain
43	chr6:147649600-147679800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr6:147649600-147680200	Weak transcription	Fetal Intestine Small	intestine
45	chr6:147649600-147680200	Weak transcription	NHLF	lung
46	chr6:147649600-147684000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr6:147649600-147685200	Weak transcription	Fetal Lung	lung
48	chr6:147649600-147703800	Weak transcription	Fetal Stomach	stomach
49	chr6:147649600-147706000	Weak transcription	Fetal Kidney	kidney
50	chr6:147649600-147711800	Weak transcription	Colonic Mucosa	Colon

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