Variant report

Variant	nsv870164
Chromosome Location	chr8:61484657-61529482
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	ATF1	chr8:61488536-61488813	K562	blood:	n/a	n/a
2	BHLHE40	chr8:61488521-61488822	K562	blood:	n/a	n/a
3	BHLHE40	chr8:61523592-61523794	K562	blood:	n/a	n/a
4	CBX3	chr8:61517638-61518060	K562	blood:	n/a	n/a
5	CBX3	chr8:61488467-61488745	K562	blood:	n/a	n/a
6	CBX3	chr8:61517736-61517998	K562	blood:	n/a	n/a
7	CCNT2	chr8:61488521-61488807	K562	blood:	n/a	n/a
8	CEBPB	chr8:61496425-61496755	IMR90	lung:	n/a	n/a
9	CEBPB	chr8:61496430-61496700	HepG2	liver:	n/a	n/a
10	CEBPB	chr8:61496325-61496747	MCF-7	breast:	n/a	n/a
11	CEBPB	chr8:61488465-61488752	K562	blood:	n/a	n/a
12	CEBPB	chr8:61496436-61496730	A549	lung:	n/a	n/a
13	CEBPB	chr8:61526369-61526821	A549	lung:	n/a	n/a
14	CEBPD	chr8:61488390-61488820	K562	blood:	n/a	n/a
15	CEBPD	chr8:61488483-61488930	K562	blood:	n/a	n/a
16	CTCF	chr8:61523669-61523882	GM13977	blood:	n/a	n/a
17	CTCF	chr8:61523668-61523822	MCF-7	breast:	n/a	n/a
18	CTCF	chr8:61523700-61523850	GM12866	blood:	n/a	n/a
19	CTCF	chr8:61523660-61523810	HMF	breast:	n/a	n/a
20	CTCF	chr8:61526480-61526630	GM12878	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
21	CTCF	chr8:61526420-61526570	BE2_C	brain:	n/a	n/a
22	CTCF	chr8:61523660-61523810	GM12867	blood:	n/a	n/a
23	CTCF	chr8:61526560-61526710	HCM	heart:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
24	CTCF	chr8:61520200-61520350	GM12869	blood:	n/a	n/a
25	CTCF	chr8:61526480-61526630	Hela-S3	cervix:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
26	CTCF	chr8:61526460-61526610	GM12870	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
27	CTCF	chr8:61526520-61526670	HPF	lung:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
28	CTCF	chr8:61523680-61523830	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr8:61526920-61527070	NHEK	skin:	n/a	n/a
30	CTCF	chr8:61526389-61526731	K562	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
31	CTCF	chr8:61526520-61526670	RPTEC	kidney:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
32	CTCF	chr8:61523618-61523907	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:61523660-61523810	AG04449	skin:	n/a	n/a
34	CTCF	chr8:61526490-61526626	MCF-7	breast:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
35	CTCF	chr8:61526477-61526688	GM12878	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
36	CTCF	chr8:61497940-61498090	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr8:61523640-61523790	NHLF	lung:	n/a	n/a
38	CTCF	chr8:61523664-61523842	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:61526740-61526890	BE2_C	brain:	n/a	n/a
40	CTCF	chr8:61523524-61523949	GM12878	blood:	n/a	n/a
41	CTCF	chr8:61526425-61526828	MCF-7	breast:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
42	CTCF	chr8:61523660-61523810	GM12873	blood:	n/a	n/a
43	CTCF	chr8:61526560-61526710	RPTEC	kidney:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
44	CTCF	chr8:61523960-61524110	GM12878	blood:	n/a	n/a
45	CTCF	chr8:61526460-61526610	HCM	heart:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
46	CTCF	chr8:61526510-61526621	SK-N-SH_RA	brain:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
47	CTCF	chr8:61526520-61526670	HEEpiC	esophagus:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
48	CTCF	chr8:61523720-61523870	GM12864	blood:	n/a	n/a
49	CTCF	chr8:61523680-61523830	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr8:61523700-61523850	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:61496287-61496337	NHBE	bronchial:	n/a
2	chr8:61496287-61496337	AG04450	lung:	fetal
3	chr8:61496287-61496337	NT2-D1	testis:	n/a
4	chr8:61496287-61496337	AG10803	skin:	n/a
5	chr8:61496287-61496337	HEK293	kidney:	embryo
6	chr8:61496287-61496337	HRE	kidney:	n/a
7	chr8:61496287-61496337	BE2_C	brain:	n/a
8	chr8:61496287-61496337	GM12892	blood:	n/a
9	chr8:61496287-61496337	LNCaP	prostate:	n/a
10	chr8:61496287-61496337	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:61496287-61496337	HCPEpiC	choroid plexus:	n/a
12	chr8:61496287-61496337	NH-A	brain:	n/a
13	chr8:61496287-61496337	HEEpiC	esophagus:	n/a
14	chr8:61496287-61496337	PFSK-1	brain:	n/a
15	chr8:61496287-61496337	GM12878	blood:	n/a
16	chr8:61496287-61496337	ovcar-3	ovarian:	n/a
17	chr8:61496287-61496337	A549	lung:	n/a
18	chr8:61496287-61496337	HRCEpiC	kidney:	n/a
19	chr8:61496287-61496337	MCF-7	breast:	n/a
20	chr8:61496287-61496337	AG09319	gingival:	n/a
21	chr8:61496287-61496337	HMEC	breast:	n/a
22	chr8:61496287-61496337	H1-hESC	embryonic stem cell:	embryo
23	chr8:61496287-61496337	PrEC	prostate:	n/a
24	chr8:61496287-61496337	IMR90	lung:	fetal
25	chr8:61496287-61496337	T-47D	breast:	n/a
26	chr8:61496287-61496337	GM12891	blood:	n/a
27	chr8:61496287-61496337	ECC-1	luminal epithelium:	n/a
28	chr8:61496287-61496337	MCF10A-Er-Src	breast:	n/a
29	chr8:61496287-61496337	Hepatocyte	liver:	n/a
30	chr8:61496287-61496337	HCF	heart:	n/a
31	chr8:61496287-61496337	CMK	blood:	n/a
32	chr8:61496287-61496337	K562	blood:	n/a
33	chr8:61496287-61496337	AG04449	skin:	fetal
34	chr8:61496287-61496337	HCM	heart:	n/a
35	chr8:61496287-61496337	SK-N-MC	brain:	n/a
36	chr8:61496287-61496337	HCT-116	colon:	n/a
37	chr8:61496287-61496337	HNPCEpiC	eye:	n/a
38	chr8:61496287-61496337	GM19239	blood:	n/a
39	chr8:61496287-61496337	AG09309	skin:	n/a
40	chr8:61496287-61496337	U87	brain:	n/a
41	chr8:61496287-61496337	SK-N-SH_RA	brain:	n/a
42	chr8:61496287-61496337	SK-N-SH	brain:	n/a
43	chr8:61496287-61496337	PANC-1	pancreas:	n/a
44	chr8:61496287-61496337	HL-60	blood:	n/a
45	chr8:61496287-61496337	HepG2	liver:	n/a
46	chr8:61496287-61496337	Caco-2	colon:	n/a
47	chr8:61496287-61496337	NHDF-neo	bronchial:	n/a
48	chr8:61496287-61496337	HRPEpiC	eye:	n/a
49	chr8:61496287-61496337	NB4	blood:	n/a
50	chr8:61496287-61496337	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:61385902..61386459-chr8:61523291..61524223,2	MCF-7	breast:
2	chr8:61499691..61501377-chr8:61506333..61508356,2	MCF-7	breast:
3	chr8:61520531..61524778-chr8:61525857..61529848,4	K562	blood:
4	chr8:61527789..61530559-chr8:61535884..61538190,2	K562	blood:
5	chr8:61511100..61513643-chr8:61515847..61518764,3	MCF-7	breast:
6	chr8:61324832..61325643-chr8:61526141..61526863,2	MCF-7	breast:
7	chr8:61494128..61496652-chr8:61499628..61502002,2	MCF-7	breast:
8	chr8:60964757..60965301-chr8:61523482..61524287,2	MCF-7	breast:
9	chr8:61506351..61508434-chr8:61511898..61514412,2	K562	blood:
10	chr8:61521815..61524778-chr8:61526470..61529848,3	K562	blood:
11	chr8:61525760..61527520-chr8:61863383..61865720,2	K562	blood:
12	chr8:61490038..61491609-chr8:61491696..61493225,2	K562	blood:
13	chr8:61511100..61513643-chr8:61515847..61518764,3	MCF-7	breast:
14	chr8:61491953..61494205-chr8:61500253..61502240,2	K562	blood:
15	chr8:61519878..61522634-chr8:61564445..61566821,2	MCF-7	breast:
16	chr8:61483782..61485918-chr8:61489573..61491999,2	K562	blood:
17	chr8:61525465..61527090-chr8:61529519..61532324,2	K562	blood:
18	chr8:61525459..61529300-chr8:61532493..61534738,4	K562	blood:
19	chr8:61490038..61491609-chr8:61491696..61493225,2	K562	blood:
20	chr8:61506351..61508434-chr8:61511898..61514412,2	K562	blood:
21	chr8:61428598..61430865-chr8:61522544..61524391,2	MCF-7	breast:
22	chr8:61527800..61530109-chr8:61531903..61534207,2	K562	blood:
23	chr8:61499691..61501377-chr8:61506333..61508356,2	MCF-7	breast:
24	chr8:61324681..61325874-chr8:61523253..61524359,7	K562	blood:
25	chr8:61324855..61325726-chr8:61523264..61524233,4	MCF-7	breast:
26	chr8:61485932..61488499-chr8:61490166..61492384,2	K562	blood:
27	chr8:61441838..61443527-chr8:61486659..61489457,2	MCF-7	breast:
28	chr8:61486393..61488900-chr8:61501099..61503900,2	K562	blood:
29	chr8:61524875..61526902-chr8:61529551..61531219,2	K562	blood:
30	chr8:61496184..61498168-chr8:61505119..61506811,2	MCF-7	breast:
31	chr8:61520531..61524778-chr8:61525857..61529848,4	K562	blood:
32	chr8:61491953..61494205-chr8:61500253..61502240,2	K562	blood:
33	chr8:61521815..61524778-chr8:61526470..61529848,3	K562	blood:
34	chr8:61485932..61488499-chr8:61490166..61492384,2	K562	blood:
35	chr8:61525175..61527465-chr8:61536083..61538610,2	K562	blood:
36	chr8:61479439..61481118-chr8:61492027..61494400,2	K562	blood:
37	chr8:61385346..61386405-chr8:61523298..61524048,5	K562	blood:
38	chr8:61427063..61431145-chr8:61524680..61528238,3	MCF-7	breast:
39	chr8:61483782..61485918-chr8:61489573..61491999,2	K562	blood:
40	chr8:61486393..61488900-chr8:61501099..61503900,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CA8-11	chr8:61488669-61488931	ucscGeneNc_uc003xuc_1

Variant related genes	Relation type
RAB2A	TF binding region
RAB2A	CpG island
ENSG00000251396	chromatin interactions
ENSG00000254869	chromatin interactions
ENSG00000104388	chromatin interactions

Extended variants
information (count: 1762 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1762 , 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	rs561670645	chr8:61484695-61484696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186158413	chr8:61484700-61484701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371695881	chr8:61484703-61484704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs3735825	chr8:61484788-61484789	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs11987024	chr8:61484799-61484800	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533054205	chr8:61484837-61484838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551572546	chr8:61484850-61484851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566509904	chr8:61484861-61484862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190322306	chr8:61484882-61484883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549116005	chr8:61484899-61484900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150649577	chr8:61484948-61484949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77221358	chr8:61484950-61484951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116642631	chr8:61484957-61484958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578213813	chr8:61484974-61484975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201794826	chr8:61485059-61485060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538930629	chr8:61485072-61485073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568981486	chr8:61485084-61485085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537976370	chr8:61485088-61485089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554352325	chr8:61485118-61485119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs16926294	chr8:61485137-61485138	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182920242	chr8:61485256-61485257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187637303	chr8:61485293-61485294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573761177	chr8:61485314-61485315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544220125	chr8:61485366-61485367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562314750	chr8:61485368-61485369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139765167	chr8:61485409-61485410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544929959	chr8:61485495-61485496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs118152200	chr8:61485496-61485497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190955130	chr8:61485526-61485527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548754525	chr8:61485559-61485560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56294255	chr8:61485570-61485571	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs531665520	chr8:61485574-61485575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs56123131	chr8:61485575-61485576	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs539599999	chr8:61485592-61485593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73259499	chr8:61485595-61485596	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs62510249	chr8:61485630-61485631	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs201325286	chr8:61485637-61485638	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199777515	chr8:61485639-61485640	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200330321	chr8:61485640-61485641	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201464452	chr8:61485641-61485642	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs66607995	chr8:61485642-61485643	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs55755153	chr8:61485644-61485645	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376331590	chr8:61485706-61485707	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530903431	chr8:61485714-61485715	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183593564	chr8:61485751-61485752	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187831668	chr8:61485789-61485790	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371008731	chr8:61485847-61485848	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146917947	chr8:61485857-61485858	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573800401	chr8:61485872-61485873	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs199642878	chr8:61485905-61485906	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61438000-61488600	Weak transcription	Fetal Brain Female	brain
2	chr8:61439400-61494600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:61448600-61505400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:61458200-61497000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:61459400-61495800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr8:61466400-61516800	Weak transcription	Stomach Mucosa	stomach
7	chr8:61467200-61515400	Weak transcription	Fetal Brain Male	brain
8	chr8:61468800-61488600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr8:61469000-61495000	Weak transcription	Brain Germinal Matrix	brain
10	chr8:61469400-61488600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr8:61472000-61488800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:61473200-61489200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:61473600-61493800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr8:61473600-61495000	Weak transcription	Spleen	Spleen
15	chr8:61473600-61497800	Weak transcription	Lung	lung
16	chr8:61474200-61485600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr8:61474200-61504000	Weak transcription	Colon Smooth Muscle	Colon
18	chr8:61474400-61486600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr8:61474600-61496200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr8:61474600-61496400	Weak transcription	Thymus	Thymus
21	chr8:61474800-61485600	Weak transcription	Small Intestine	intestine
22	chr8:61474800-61496000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr8:61474800-61504000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr8:61475000-61493600	Weak transcription	Fetal Kidney	kidney
25	chr8:61475000-61495600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr8:61475400-61494600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr8:61475400-61498200	Weak transcription	A549	lung
28	chr8:61476200-61488600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr8:61476200-61488600	Weak transcription	Fetal Heart	heart
30	chr8:61476200-61495400	Weak transcription	Hela-S3	cervix
31	chr8:61476200-61504800	Weak transcription	NHLF	lung
32	chr8:61476200-61517000	Weak transcription	Brain Angular Gyrus	brain
33	chr8:61476400-61495400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr8:61476400-61496400	Weak transcription	Brain Substantia Nigra	brain
35	chr8:61476600-61487800	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr8:61476600-61488400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:61476600-61488600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr8:61476600-61495400	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr8:61476800-61485600	Weak transcription	Adipose Nuclei	Adipose
40	chr8:61476800-61485800	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr8:61476800-61488400	Weak transcription	K562	blood
42	chr8:61476800-61488800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr8:61476800-61495200	Weak transcription	Brain Anterior Caudate	brain
44	chr8:61477000-61485800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr8:61477000-61495000	Weak transcription	Ovary	ovary
46	chr8:61477200-61491200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:61477200-61494600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr8:61477400-61497600	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr8:61477600-61485800	Weak transcription	NH-A	brain
50	chr8:61477800-61485600	Weak transcription	Primary T helper cells fromperipheralblood	blood

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