Variant report

Variant	esv1835162
Chromosome Location	chr8:8745741-8758058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:668)
CpG islands
(count:1221)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8745634-8745915	HepG2	liver:	n/a	n/a
2	ATF3	chr8:8750940-8751242	GM12878	blood:	n/a	chr8:8751163-8751183
3	ATF3	chr8:8750978-8751250	K562	blood:	n/a	chr8:8751163-8751183
4	ATF3	chr8:8750978-8751243	H1-hESC	embryonic stem cell:	n/a	chr8:8751163-8751183
5	ATF3	chr8:8750950-8751310	HepG2	liver:	n/a	chr8:8751163-8751183
6	ATF3	chr8:8751036-8751247	GM12878	blood:	n/a	chr8:8751163-8751183
7	BACH1	chr8:8751398-8751562	K562	blood:	n/a	n/a
8	BACH1	chr8:8751377-8751489	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:8753115-8753116	K562	blood:	n/a	n/a
10	BATF	chr8:8746648-8746919	GM12878	blood:	n/a	chr8:8746803-8746814
11	BCLAF1	chr8:8750870-8751214	GM12878	blood:	n/a	chr8:8751147-8751160 chr8:8750943-8750956
12	BHLHE40	chr8:8750339-8750646	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:8745720-8746081	HepG2	liver:	n/a	n/a
14	BHLHE40	chr8:8747792-8747920	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:8750995-8751344	HepG2	liver:	n/a	chr8:8751138-8751154 chr8:8751144-8751160 chr8:8751161-8751174
16	BHLHE40	chr8:8750981-8751590	K562	blood:	n/a	chr8:8751138-8751154 chr8:8751144-8751160 chr8:8751161-8751174
17	BHLHE40	chr8:8745821-8746045	K562	blood:	n/a	n/a
18	BHLHE40	chr8:8745703-8745989	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:8750308-8750515	K562	blood:	n/a	n/a
20	BHLHE40	chr8:8750970-8751320	GM12878	blood:	n/a	chr8:8751138-8751154 chr8:8751144-8751160 chr8:8751161-8751174
21	BRCA1	chr8:8746647-8746978	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr8:8751348-8751425	Hela-S3	cervix:	n/a	n/a
23	CCNT2	chr8:8750298-8751487	K562	blood:	n/a	n/a
24	CEBPB	chr8:8745755-8746029	HepG2	liver:	n/a	chr8:8745887-8745900
25	CEBPB	chr8:8745860-8745984	H1-hESC	embryonic stem cell:	n/a	chr8:8745887-8745900
26	CEBPB	chr8:8746631-8747089	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr8:8746698-8746971	Hela-S3	cervix:	n/a	n/a
28	CEBPD	chr8:8750872-8751206	HepG2	liver:	n/a	n/a
29	CHD1	chr8:8751464-8751820	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr8:8751088-8751115	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr8:8749977-8750570	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr8:8750408-8750567	GM12878	blood:	n/a	n/a
33	CHD2	chr8:8751396-8751565	K562	blood:	n/a	n/a
34	CHD2	chr8:8749654-8750359	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr8:8750843-8751239	Hela-S3	cervix:	n/a	n/a
36	CREB1	chr8:8750429-8750881	A549	lung:	n/a	n/a
37	CREB1	chr8:8750955-8751370	A549	lung:	n/a	n/a
38	CTCF	chr8:8751127-8751193	HUVEC	blood vessel:	n/a	chr8:8751142-8751155
39	CTCF	chr8:8751000-8751150	GM12874	blood:	n/a	n/a
40	CTCF	chr8:8749520-8749670	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr8:8750200-8750350	HepG2	liver:	n/a	n/a
42	CTCF	chr8:8749740-8749890	GM12864	blood:	n/a	n/a
43	CTCF	chr8:8751001-8751263	K562	blood:	n/a	chr8:8751142-8751155
44	CTCF	chr8:8750600-8750750	GM12868	blood:	n/a	n/a
45	CTCF	chr8:8749660-8749810	GM12871	blood:	n/a	n/a
46	CTCF	chr8:8751132-8751173	HepG2	liver:	n/a	chr8:8751142-8751155
47	CTCF	chr8:8750640-8750790	GM12871	blood:	n/a	n/a
48	CTCF	chr8:8749646-8749709	GM12892	blood:	n/a	n/a
49	CTCF	chr8:8749674-8749729	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr8:8750836-8751314	GM12878	blood:	n/a	chr8:8751142-8751155

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8746679-8746729	ProgFib	skin:	n/a
2	chr8:8746679-8746729	ProgFib	skin:	n/a
3	chr8:8749343-8749393	U87	brain:	n/a
4	chr8:8752348-8752398	HCF	heart:	n/a
5	chr8:8747452-8747502	HEEpiC	esophagus:	n/a
6	chr8:8748792-8748842	MCF-7	breast:	n/a
7	chr8:8745938-8745988	PFSK-1	brain:	n/a
8	chr8:8749938-8749988	PrEC	prostate:	n/a
9	chr8:8751325-8751375	GM12891	blood:	n/a
10	chr8:8751477-8751527	SK-N-SH_RA	brain:	n/a
11	chr8:8746679-8746729	AG09309	skin:	n/a
12	chr8:8755272-8755322	SK-N-MC	brain:	n/a
13	chr8:8749278-8749328	AG10803	skin:	n/a
14	chr8:8749074-8749124	HCPEpiC	choroid plexus:	n/a
15	chr8:8749074-8749124	NT2-D1	testis:	n/a
16	chr8:8750314-8750364	SK-N-SH_RA	brain:	n/a
17	chr8:8755272-8755322	NB4	blood:	n/a
18	chr8:8751498-8751548	ECC-1	luminal epithelium:	n/a
19	chr8:8749343-8749393	AoSMC	blood vessel:	n/a
20	chr8:8750314-8750364	T-47D	breast:	n/a
21	chr8:8751477-8751527	BJ	skin:	n/a
22	chr8:8752348-8752398	HUVEC	blood vessel:	n/a
23	chr8:8749343-8749393	GM06990	blood:	n/a
24	chr8:8748536-8748586	Hela-S3	cervix:	n/a
25	chr8:8752348-8752398	IMR90	lung:	fetal
26	chr8:8749278-8749328	NHDF-neo	bronchial:	n/a
27	chr8:8749074-8749124	BJ	skin:	n/a
28	chr8:8750517-8750567	GM06990	blood:	n/a
29	chr8:8750314-8750364	HCF	heart:	n/a
30	chr8:8749494-8749544	SK-N-SH_RA	brain:	n/a
31	chr8:8747297-8747347	HEEpiC	esophagus:	n/a
32	chr8:8745938-8745988	HNPCEpiC	eye:	n/a
33	chr8:8750517-8750567	AG09319	gingival:	n/a
34	chr8:8746679-8746729	HCT-116	colon:	n/a
35	chr8:8748536-8748586	NB4	blood:	n/a
36	chr8:8751325-8751375	HRCEpiC	kidney:	n/a
37	chr8:8745938-8745988	RPTEC	kidney:	n/a
38	chr8:8749919-8749969	HAEpiC	amniotic membrane:	n/a
39	chr8:8752348-8752398	U87	brain:	n/a
40	chr8:8755272-8755322	HRCEpiC	kidney:	n/a
41	chr8:8749919-8749969	H1-hESC	embryonic stem cell:	embryo
42	chr8:8749074-8749124	SKMC	muscle:	n/a
43	chr8:8748536-8748586	U87	brain:	n/a
44	chr8:8749938-8749988	NB4	blood:	n/a
45	chr8:8751498-8751548	HAEpiC	amniotic membrane:	n/a
46	chr8:8748536-8748586	AG09309	skin:	n/a
47	chr8:8748792-8748842	HRPEpiC	eye:	n/a
48	chr8:8749494-8749544	AG04450	lung:	fetal
49	chr8:8749494-8749544	Jurkat	blood:	n/a
50	chr8:8747452-8747502	AG09309	skin:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8750920..8752897-chr8:8753485..8755610,2	MCF-7	breast:
2	chr8:8678713..8680298-chr8:8749363..8750992,2	MCF-7	breast:
3	chr8:8733670..8736303-chr8:8745304..8747711,2	K562	blood:
4	chr8:8640474..8642635-chr8:8745832..8748288,2	MCF-7	breast:
5	chr8:8678976..8682016-chr8:8748981..8752043,3	MCF-7	breast:
6	chr8:8748349..8752697-chr8:8864961..8869329,4	K562	blood:
7	chr8:8647143..8649997-chr8:8748170..8750908,2	MCF-7	breast:
8	chr8:8738833..8741293-chr8:8745302..8747462,3	K562	blood:
9	chr8:8676467..8679551-chr8:8749550..8751180,3	K562	blood:
10	chr8:8743895..8745799-chr8:8861981..8863756,2	K562	blood:
11	chr8:8751885..8754509-chr8:8756832..8758462,2	MCF-7	breast:
12	chr8:8726269..8728991-chr8:8747261..8749561,2	K562	blood:
13	chr8:8715858..8717945-chr8:8749655..8752629,2	K562	blood:
14	chr8:8756284..8757870-chr8:8861137..8863458,2	K562	blood:
15	chr8:8742135..8744016-chr8:8747118..8749376,2	K562	blood:
16	chr8:8749232..8754669-chr8:8756372..8762618,9	MCF-7	breast:
17	chr8:8707079..8709143-chr8:8751442..8753018,2	MCF-7	breast:
18	chr8:8637079..8641758-chr8:8747812..8752273,5	MCF-7	breast:

No data

Variant related genes	Relation type
MFHAS1	TF binding region
RNU6-682P	TF binding region
MFHAS1	CpG island
RNU6-682P	CpG island
ENSG00000200713	chromatin interactions
ENSG00000147324	chromatin interactions
ENSG00000104626	chromatin interactions
ENSG00000254367	chromatin interactions

Extended variants
information (count: 677 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7013902	chr8:8745741-8745742	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186873156	chr8:8745743-8745744	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs73662205	chr8:8745766-8745767	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs191304776	chr8:8745780-8745781	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs35736441	chr8:8745783-8745784	Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs138488823	chr8:8745824-8745825	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs376293632	chr8:8745846-8745847	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs183059832	chr8:8745865-8745866	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs539766797	chr8:8745879-8745880	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs556083370	chr8:8745882-8745883	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs575950044	chr8:8745925-8745926	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs560624003	chr8:8745931-8745932	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs58511457	chr8:8745939-8745940	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs555082078	chr8:8745953-8745954	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs576188983	chr8:8745977-8745978	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs73192219	chr8:8745992-8745993	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs540852494	chr8:8746015-8746016	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs563959579	chr8:8746023-8746024	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs150661228	chr8:8746027-8746028	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs113065905	chr8:8746028-8746029	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs60822177	chr8:8746050-8746051	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs10107645	chr8:8746051-8746052	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs559771363	chr8:8746058-8746059	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs543364016	chr8:8746081-8746082	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs562856567	chr8:8746098-8746099	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs531658160	chr8:8746111-8746112	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs537266326	chr8:8746126-8746127	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs548693274	chr8:8746201-8746202	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs187710177	chr8:8746204-8746205	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs527867509	chr8:8746217-8746218	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs547983521	chr8:8746272-8746273	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs557607242	chr8:8746282-8746283	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs191289917	chr8:8746295-8746296	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs73662206	chr8:8746298-8746299	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs527495853	chr8:8746356-8746357	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs148324864	chr8:8746383-8746384	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs569623049	chr8:8746390-8746391	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs182351755	chr8:8746427-8746428	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs561025139	chr8:8746431-8746432	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs530034089	chr8:8746432-8746433	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs10092694	chr8:8746446-8746447	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532834928	chr8:8746462-8746463	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs187728309	chr8:8746468-8746469	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs557492151	chr8:8746477-8746478	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs370468832	chr8:8746522-8746523	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs577766802	chr8:8746529-8746530	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs66863310	chr8:8746534-8746535	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs374759708	chr8:8746539-8746540	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs116438233	chr8:8746540-8746541	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs398086328	chr8:8746553-8746554	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Gastric cancer	17229543	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8730800-8747600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr8:8735800-8746200	Weak transcription	Esophagus	oesophagus
3	chr8:8738600-8745800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr8:8739200-8746800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr8:8740400-8745800	Weak transcription	Placenta	Placenta
6	chr8:8742400-8745800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:8742400-8745800	Weak transcription	Lung	lung
8	chr8:8742600-8745800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:8742600-8745800	Weak transcription	Fetal Muscle Leg	muscle
10	chr8:8742600-8745800	Weak transcription	Gastric	stomach
11	chr8:8742600-8747200	Weak transcription	Spleen	Spleen
12	chr8:8742800-8745800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:8742800-8746200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr8:8743200-8748200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:8743800-8745800	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr8:8744000-8747600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:8744600-8745800	Weak transcription	Pancreas	Pancrea
18	chr8:8745000-8747000	Active TSS	Fetal Brain Male	brain
19	chr8:8745200-8745800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
20	chr8:8745200-8745800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr8:8745200-8745800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr8:8745200-8745800	Active TSS	Colonic Mucosa	Colon
23	chr8:8745200-8745800	Enhancers	Fetal Stomach	stomach
24	chr8:8745200-8745800	Transcr. at gene 5' and 3'	K562	blood
25	chr8:8745200-8746000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr8:8745200-8746000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr8:8745200-8746000	Flanking Active TSS	Fetal Intestine Large	intestine
28	chr8:8745200-8746200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:8745200-8746400	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:8745200-8746400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr8:8745200-8746400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr8:8745200-8746400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr8:8745200-8746400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
34	chr8:8745200-8746400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr8:8745200-8746400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
36	chr8:8745200-8746400	Flanking Active TSS	HepG2	liver
37	chr8:8745200-8746400	Flanking Active TSS	Osteobl	bone
38	chr8:8745200-8746600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr8:8745200-8746800	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr8:8745200-8747000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr8:8745200-8747200	Active TSS	H1 Cell Line	embryonic stem cell
42	chr8:8745200-8747200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:8745200-8747200	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr8:8745200-8747200	Active TSS	NHLF	lung
45	chr8:8745200-8747800	Active TSS	Brain Hippocampus Middle	brain
46	chr8:8745200-8747800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr8:8745200-8748600	Enhancers	Primary B cells from peripheral blood	blood
48	chr8:8745200-8749000	Active TSS	Brain Substantia Nigra	brain
49	chr8:8745200-8749200	Active TSS	Brain Angular Gyrus	brain
50	chr8:8745200-8749200	Active TSS	Brain Cingulate Gyrus	brain

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