Variant report

Variant	nsv437525
Chromosome Location	chr6:146212285-146230454
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	chr6:146214733-146214978	K562	blood:	n/a	n/a
2	ARID3A	chr6:146216946-146217259	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:146216956-146217248	K562	blood:	n/a	n/a
4	ATF1	chr6:146226877-146227168	K562	blood:	n/a	n/a
5	ATF1	chr6:146214733-146215087	K562	blood:	n/a	n/a
6	BHLHE40	chr6:146214806-146215003	K562	blood:	n/a	n/a
7	BHLHE40	chr6:146212488-146212582	HepG2	liver:	n/a	n/a
8	CBX3	chr6:146218650-146219020	K562	blood:	n/a	n/a
9	CCNT2	chr6:146223331-146223531	K562	blood:	n/a	chr6:146223440-146223460
10	CEBPB	chr6:146212289-146213099	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:146212225-146213135	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:146219612-146219900	IMR90	lung:	n/a	n/a
13	CREB1	chr6:146214732-146215104	K562	blood:	n/a	n/a
14	CREB1	chr6:146214578-146215201	K562	blood:	n/a	n/a
15	CTCF	chr6:146217060-146217210	HRE	kidney:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
16	CTCF	chr6:146217020-146217170	NB4	blood:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
17	CTCF	chr6:146217040-146217190	HVMF	connective:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
18	CTCF	chr6:146217020-146217170	AG10803	skin:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
19	CTCF	chr6:146217060-146217210	HCPEpiC	choroid plexus:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
20	CTCF	chr6:146217051-146217151	LNCaP	prostate:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
21	CTCF	chr6:146217000-146217150	RPTEC	kidney:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
22	CTCF	chr6:146217000-146217150	GM06990	blood:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
23	CTCF	chr6:146217000-146217150	AG04450	lung:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
24	CTCF	chr6:146226940-146227090	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr6:146217000-146217150	AG04449	skin:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
26	CTCF	chr6:146217107-146217132	GM13976	blood:	n/a	chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
27	CTCF	chr6:146225784-146225822	GM13976	blood:	n/a	n/a
28	CTCF	chr6:146226997-146227065	ProgFib	skin:	n/a	n/a
29	CTCF	chr6:146217020-146217170	HMF	breast:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
30	CTCF	chr6:146226983-146227073	Gliobla	brain:	n/a	n/a
31	CTCF	chr6:146216980-146217130	AG09309	skin:	n/a	chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
32	CTCF	chr6:146217060-146217210	AoAF	blood vessel:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
33	CTCF	chr6:146217000-146217150	NHLF	lung:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
34	CTCF	chr6:146217060-146217210	GM12873	blood:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
35	CTCF	chr6:146217087-146217207	LNCaP	prostate:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
36	CTCF	chr6:146217040-146217190	HCPEpiC	choroid plexus:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
37	CTCF	chr6:146227000-146227150	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr6:146216980-146217130	HCFaa	heart:	n/a	chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
39	CTCF	chr6:146217040-146217190	AG09319	gingival:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
40	CTCF	chr6:146226900-146227050	GM06990	blood:	n/a	chr6:146226928-146226936
41	CTCF	chr6:146217040-146217190	HUVEC	blood vessel:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
42	CTCF	chr6:146217040-146217190	HA-sp	spinal cord:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
43	CTCF	chr6:146227020-146227064	HepG2	liver:	n/a	n/a
44	CTCF	chr6:146217060-146217210	WI-38	lung:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
45	CTCF	chr6:146226920-146227070	AG09319	gingival:	n/a	chr6:146226928-146226936
46	CTCF	chr6:146217040-146217190	SAEC	small airway:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126
47	CTCF	chr6:146217160-146217310	NHEK	skin:	n/a	n/a
48	CTCF	chr6:146227018-146227118	K562	blood:	n/a	n/a
49	CTCF	chr6:146226908-146227192	K562	blood:	n/a	chr6:146226928-146226936
50	CTCF	chr6:146217060-146217210	AG09309	skin:	n/a	chr6:146217112-146217133 chr6:146217111-146217127 chr6:146217110-146217128 chr6:146217113-146217126

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:146212966-146213016	HepG2	liver:	n/a
2	chr6:146212966-146213016	AoSMC	blood vessel:	n/a
3	chr6:146212966-146213016	IMR90	lung:	fetal
4	chr6:146212966-146213016	AG04450	lung:	fetal
5	chr6:146212966-146213016	HCPEpiC	choroid plexus:	n/a
6	chr6:146212966-146213016	HRE	kidney:	n/a
7	chr6:146212966-146213016	U87	brain:	n/a
8	chr6:146212966-146213016	RPTEC	kidney:	n/a
9	chr6:146212966-146213016	HRPEpiC	eye:	n/a
10	chr6:146212966-146213016	SAEC	small airway:	n/a
11	chr6:146212966-146213016	BJ	skin:	n/a
12	chr6:146212966-146213016	HNPCEpiC	eye:	n/a
13	chr6:146212966-146213016	NHBE	bronchial:	n/a
14	chr6:146212966-146213016	SK-N-SH_RA	brain:	n/a
15	chr6:146212966-146213016	Hela-S3	cervix:	n/a
16	chr6:146212966-146213016	HAEpiC	amniotic membrane:	n/a
17	chr6:146212966-146213016	PFSK-1	brain:	n/a
18	chr6:146212966-146213016	PANC-1	pancreas:	n/a
19	chr6:146212966-146213016	HL-60	blood:	n/a
20	chr6:146212966-146213016	GM12892	blood:	n/a
21	chr6:146212966-146213016	HCF	heart:	n/a
22	chr6:146212966-146213016	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:146212966-146213016	GM19239	blood:	n/a
24	chr6:146212966-146213016	HEK293	kidney:	embryo
25	chr6:146212966-146213016	HRCEpiC	kidney:	n/a
26	chr6:146212966-146213016	GM12891	blood:	n/a
27	chr6:146212966-146213016	K562	blood:	n/a
28	chr6:146212966-146213016	HMEC	breast:	n/a
29	chr6:146212966-146213016	NT2-D1	testis:	n/a
30	chr6:146212966-146213016	AG10803	skin:	n/a
31	chr6:146212966-146213016	ovcar-3	ovarian:	n/a
32	chr6:146212966-146213016	ECC-1	luminal epithelium:	n/a
33	chr6:146212966-146213016	GM12878	blood:	n/a
34	chr6:146212966-146213016	NHDF-neo	bronchial:	n/a
35	chr6:146212966-146213016	CMK	blood:	n/a
36	chr6:146212966-146213016	NH-A	brain:	n/a
37	chr6:146212966-146213016	H1-hESC	embryonic stem cell:	embryo
38	chr6:146212966-146213016	HEEpiC	esophagus:	n/a
39	chr6:146212966-146213016	SK-N-MC	brain:	n/a
40	chr6:146212966-146213016	LNCaP	prostate:	n/a
41	chr6:146212966-146213016	T-47D	breast:	n/a
42	chr6:146212966-146213016	MCF-7	breast:	n/a
43	chr6:146212966-146213016	HIPEpiC	eye:	n/a
44	chr6:146212966-146213016	A549	lung:	n/a
45	chr6:146212966-146213016	HCM	heart:	n/a
46	chr6:146212966-146213016	Jurkat	blood:	n/a
47	chr6:146212966-146213016	HUVEC	blood vessel:	n/a
48	chr6:146212966-146213016	PrEC	prostate:	n/a
49	chr6:146212966-146213016	BE2_C	brain:	n/a
50	chr6:146212966-146213016	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:146208202..146210645-chr6:146210859..146213066,4	K562	blood:
2	chr6:146220104..146222683-chr6:146242186..146243850,2	K562	blood:
3	chr6:146134558..146137380-chr6:146209564..146213180,4	MCF-7	breast:
4	chr6:146204410..146206507-chr6:146211730..146213654,2	MCF-7	breast:
5	chr6:146221312..146222849-chr6:146224699..146226855,2	K562	blood:
6	chr6:146220306..146222663-chr6:146235095..146237007,2	K562	blood:
7	chr6:146133506..146135427-chr6:146211550..146213483,2	K562	blood:
8	chr6:146221103..146223678-chr6:146224120..146226593,3	K562	blood:
9	chr6:146209846..146213898-chr6:146246538..146250051,3	K562	blood:
10	chr6:146221312..146222849-chr6:146224699..146226855,2	K562	blood:
11	chr6:146133273..146135855-chr6:146228681..146230376,2	K562	blood:
12	chr6:146082619..146083392-chr6:146226555..146227506,3	MCF-7	breast:
13	chr6:146225888..146227710-chr6:146240517..146242939,2	K562	blood:
14	chr6:146221103..146223678-chr6:146224120..146226593,3	K562	blood:
15	chr6:146223378..146225845-chr6:146236858..146238625,2	K562	blood:
16	chr6:146055478..146057329-chr6:146213622..146216410,2	K562	blood:
17	chr6:146056598..146058276-chr6:146215722..146218388,2	MCF-7	breast:
18	chr6:146223883..146226442-chr6:146227329..146230872,3	K562	blood:
19	chr6:146134473..146136015-chr6:146217763..146219719,2	MCF-7	breast:
20	chr6:146223257..146225055-chr6:146864583..146866825,2	K562	blood:
21	chr6:146227271..146229515-chr6:146231026..146232898,3	K562	blood:
22	chr6:146223883..146226442-chr6:146227329..146230872,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO30-2	chr6:146216172-146218558	NONHSAT115417

Variant related genes	Relation type
SHPRH	TF binding region
SHPRH	CpG island
ENSG00000118508	chromatin interactions
ENSG00000270638	chromatin interactions
ENSG00000112425	chromatin interactions
ENSG00000235652	chromatin interactions
ENSG00000118496	chromatin interactions
ENSG00000146414	chromatin interactions

Extended variants
information (count: 641 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2265917	chr6:146212285-146212286	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531830783	chr6:146212310-146212311	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs545564559	chr6:146212311-146212312	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs2265477	chr6:146212338-146212339	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs527895626	chr6:146212405-146212406	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs541562556	chr6:146212407-146212408	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs561442429	chr6:146212417-146212418	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs184151207	chr6:146212466-146212467	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs567927777	chr6:146212528-146212529	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78321104	chr6:146212595-146212596	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs554086138	chr6:146212620-146212621	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs79545576	chr6:146212637-146212638	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs368404950	chr6:146212652-146212653	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs568561532	chr6:146212663-146212664	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs79562139	chr6:146212673-146212674	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs376897303	chr6:146212674-146212675	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs150904088	chr6:146212727-146212728	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs139425995	chr6:146212757-146212758	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs188358564	chr6:146212777-146212778	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs180923387	chr6:146212779-146212780	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs573862564	chr6:146212798-146212799	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs185971185	chr6:146212850-146212851	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs556593786	chr6:146212888-146212889	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs368714860	chr6:146213023-146213024	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs144364713	chr6:146213038-146213039	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs565393804	chr6:146213047-146213048	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs527810567	chr6:146213066-146213067	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs541597295	chr6:146213101-146213102	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs190699751	chr6:146213122-146213123	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs146129198	chr6:146213143-146213144	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs562070345	chr6:146213164-146213165	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs550067698	chr6:146213227-146213228	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140051327	chr6:146213281-146213282	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs116878912	chr6:146213328-146213329	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35144230	chr6:146213349-146213350	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182531897	chr6:146213357-146213358	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573947425	chr6:146213367-146213368	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143706939	chr6:146213397-146213398	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186417130	chr6:146213424-146213425	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547558899	chr6:146213434-146213435	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs556484400	chr6:146213449-146213450	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs190829148	chr6:146213455-146213456	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536502881	chr6:146213468-146213469	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs576478685	chr6:146213487-146213488	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576469930	chr6:146213492-146213493	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs539056110	chr6:146213539-146213540	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558715271	chr6:146213541-146213542	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572493601	chr6:146213583-146213584	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541214370	chr6:146213597-146213598	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375799496	chr6:146213605-146213606	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Lung cancer	18438408	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
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:790 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146186400-146213200	Weak transcription	Brain Anterior Caudate	brain
2	chr6:146188000-146218800	Weak transcription	Right Ventricle	heart
3	chr6:146189400-146214400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr6:146194800-146212400	Weak transcription	HUVEC	blood vessel
5	chr6:146196600-146219600	Weak transcription	HMEC	breast
6	chr6:146197800-146219600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:146198200-146212400	Weak transcription	Fetal Kidney	kidney
8	chr6:146198200-146218600	Weak transcription	Fetal Heart	heart
9	chr6:146198200-146225600	Weak transcription	HSMMtube	muscle
10	chr6:146199800-146214400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr6:146200000-146214200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr6:146200400-146228600	Weak transcription	Pancreas	Pancrea
13	chr6:146200800-146213400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr6:146201200-146217400	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:146201200-146225600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:146201200-146230400	Weak transcription	NHEK	skin
17	chr6:146201800-146219600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:146202800-146213800	Weak transcription	GM12878-XiMat	blood
19	chr6:146202800-146220000	Weak transcription	Thymus	Thymus
20	chr6:146203200-146219600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:146203400-146218600	Weak transcription	A549	lung
22	chr6:146204600-146214400	Weak transcription	Hela-S3	cervix
23	chr6:146204800-146224800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr6:146205400-146214800	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr6:146206600-146215400	Strong transcription	Adipose Nuclei	Adipose
26	chr6:146206800-146219600	Weak transcription	Fetal Intestine Small	intestine
27	chr6:146207400-146217600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:146207800-146213600	Strong transcription	Primary T cells from cord blood	blood
29	chr6:146207800-146240200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr6:146208000-146219000	Weak transcription	Small Intestine	intestine
31	chr6:146208200-146213200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr6:146208200-146215400	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr6:146208400-146215000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr6:146208400-146216800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr6:146208400-146218000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:146208400-146218800	Weak transcription	Colon Smooth Muscle	Colon
37	chr6:146208800-146213200	Strong transcription	Fetal Lung	lung
38	chr6:146208800-146215400	Strong transcription	Fetal Thymus	thymus
39	chr6:146208800-146230000	Weak transcription	Colonic Mucosa	Colon
40	chr6:146209000-146212800	Strong transcription	Duodenum Mucosa	Duodenum
41	chr6:146209000-146214800	Strong transcription	K562	blood
42	chr6:146209000-146216800	Strong transcription	Dnd41	blood
43	chr6:146209200-146215200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr6:146209400-146215000	Strong transcription	Primary B cells from cord blood	blood
45	chr6:146209400-146215200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr6:146209600-146215000	Strong transcription	Left Ventricle	heart
47	chr6:146209600-146215000	Strong transcription	Skeletal Muscle Female	skeletal muscle
48	chr6:146209800-146219000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr6:146210000-146212600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr6:146210200-146212400	Weak transcription	Primary T cells fromperipheralblood	blood

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