Variant report

Variant	nsv890338
Chromosome Location	chr8:8669622-8707970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:214)
CpG islands
(count:428)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8683384-8683480	K562	blood:	n/a	n/a
2	ATF1	chr8:8683397-8683587	K562	blood:	n/a	n/a
3	ATF2	chr8:8701553-8702169	GM12878	blood:	n/a	n/a
4	ATF2	chr8:8701550-8702012	GM12878	blood:	n/a	n/a
5	BACH1	chr8:8701480-8701772	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:8701483-8701487	K562	blood:	n/a	n/a
7	BACH1	chr8:8702394-8702415	K562	blood:	n/a	n/a
8	BATF	chr8:8706723-8707091	GM12878	blood:	n/a	n/a
9	BATF	chr8:8701577-8701988	GM12878	blood:	n/a	chr8:8701820-8701831
10	BCLAF1	chr8:8702306-8702917	K562	blood:	n/a	n/a
11	BHLHE40	chr8:8706915-8707077	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:8687310-8687552	K562	blood:	n/a	n/a
13	BHLHE40	chr8:8701873-8702139	K562	blood:	n/a	n/a
14	CBX3	chr8:8678479-8678905	K562	blood:	n/a	n/a
15	CEBPB	chr8:8701893-8702157	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr8:8683324-8683546	IMR90	lung:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
17	CEBPB	chr8:8683283-8683520	K562	blood:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
18	CEBPB	chr8:8683234-8683588	K562	blood:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
19	CEBPB	chr8:8679341-8679360	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:8690098-8690119	A549	lung:	n/a	n/a
21	CEBPB	chr8:8683232-8683571	K562	blood:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
22	CEBPB	chr8:8683208-8683648	MCF-7	breast:	n/a	chr8:8683396-8683405 chr8:8683394-8683405 chr8:8683394-8683407
23	CEBPB	chr8:8674638-8674722	A549	lung:	n/a	n/a
24	CEBPB	chr8:8691655-8692261	IMR90	lung:	n/a	n/a
25	CTCF	chr8:8679577-8679697	GM19238	blood:	n/a	n/a
26	CTCF	chr8:8691280-8691430	HepG2	liver:	n/a	n/a
27	CTCF	chr8:8679600-8679750	GM12867	blood:	n/a	n/a
28	CTCF	chr8:8679533-8679707	GM19239	blood:	n/a	n/a
29	CTCF	chr8:8679700-8679850	GM12872	blood:	n/a	n/a
30	CTCF	chr8:8679460-8679610	BE2_C	brain:	n/a	n/a
31	CUX1	chr8:8674757-8674784	K562	blood:	n/a	n/a
32	CUX1	chr8:8705436-8705687	GM12878	blood:	n/a	n/a
33	CUX1	chr8:8702569-8702948	K562	blood:	n/a	n/a
34	E2F4	chr8:8701594-8701884	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr8:8691665-8692014	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr8:8679490-8679804	GM12878	blood:	n/a	chr8:8679699-8679708 chr8:8679698-8679709 chr8:8679699-8679708 chr8:8679697-8679710
37	EBF1	chr8:8679665-8679873	GM12878	blood:	n/a	chr8:8679699-8679708 chr8:8679698-8679709 chr8:8679699-8679708 chr8:8679697-8679710
38	EBF1	chr8:8679509-8679876	GM12878	blood:	n/a	chr8:8679699-8679708 chr8:8679698-8679709 chr8:8679699-8679708 chr8:8679697-8679710
39	ELF1	chr8:8686344-8686654	K562	blood:	n/a	n/a
40	ELK1	chr8:8702485-8702521	K562	blood:	n/a	n/a
41	EP300	chr8:8686323-8686513	K562	blood:	n/a	n/a
42	EP300	chr8:8701472-8703596	SK-N-SH	brain:	n/a	chr8:8701862-8701869 chr8:8702040-8702047 chr8:8701824-8701833 chr8:8702483-8702497 chr8:8702492-8702506
43	EP300	chr8:8674696-8674963	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr8:8683362-8683606	K562	blood:	n/a	n/a
45	EP300	chr8:8695560-8695754	K562	blood:	n/a	n/a
46	EP300	chr8:8702520-8702858	GM12878	blood:	n/a	n/a
47	EP300	chr8:8701767-8702015	GM12878	blood:	n/a	chr8:8701862-8701869 chr8:8701824-8701833
48	EP300	chr8:8702480-8703021	K562	blood:	n/a	chr8:8702483-8702497 chr8:8702492-8702506
49	EP300	chr8:8702771-8703137	SK-N-SH_RA	brain:	n/a	n/a
50	EP300	chr8:8701740-8702101	Hela-S3	cervix:	n/a	chr8:8701862-8701869 chr8:8702040-8702047 chr8:8701824-8701833

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8681198-8681248	K562	blood:	n/a
2	chr8:8681198-8681248	K562	blood:	n/a
3	chr8:8702053-8702103	HCF	heart:	n/a
4	chr8:8680924-8680974	AG10803	skin:	n/a
5	chr8:8681339-8681389	HEK293	kidney:	embryo
6	chr8:8681198-8681248	AoSMC	blood vessel:	n/a
7	chr8:8679450-8679500	ovcar-3	ovarian:	n/a
8	chr8:8680924-8680974	HRPEpiC	eye:	n/a
9	chr8:8702053-8702103	GM12892	blood:	n/a
10	chr8:8681198-8681248	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:8679450-8679500	U87	brain:	n/a
12	chr8:8680903-8680953	HepG2	liver:	n/a
13	chr8:8680924-8680974	LNCaP	prostate:	n/a
14	chr8:8680924-8680974	CMK	blood:	n/a
15	chr8:8680971-8681021	AoSMC	blood vessel:	n/a
16	chr8:8681339-8681389	GM06990	blood:	n/a
17	chr8:8680903-8680953	SK-N-MC	brain:	n/a
18	chr8:8681198-8681248	SK-N-SH	brain:	n/a
19	chr8:8680924-8680974	HAEpiC	amniotic membrane:	n/a
20	chr8:8680924-8680974	ProgFib	skin:	n/a
21	chr8:8680924-8680974	AG09309	skin:	n/a
22	chr8:8680971-8681021	SK-N-MC	brain:	n/a
23	chr8:8681198-8681248	HEEpiC	esophagus:	n/a
24	chr8:8680903-8680953	BJ	skin:	n/a
25	chr8:8680903-8680953	HMEC	breast:	n/a
26	chr8:8702053-8702103	HL-60	blood:	n/a
27	chr8:8680903-8680953	GM12878	blood:	n/a
28	chr8:8680903-8680953	Hepatocyte	liver:	n/a
29	chr8:8681339-8681389	NB4	blood:	n/a
30	chr8:8702053-8702103	HCPEpiC	choroid plexus:	n/a
31	chr8:8681339-8681389	AoSMC	blood vessel:	n/a
32	chr8:8681339-8681389	SKMC	muscle:	n/a
33	chr8:8680924-8680974	HRCEpiC	kidney:	n/a
34	chr8:8702053-8702103	PrEC	prostate:	n/a
35	chr8:8680903-8680953	Hela-S3	cervix:	n/a
36	chr8:8679450-8679500	CMK	blood:	n/a
37	chr8:8680971-8681021	HCF	heart:	n/a
38	chr8:8679450-8679500	GM06990	blood:	n/a
39	chr8:8702053-8702103	NB4	blood:	n/a
40	chr8:8681198-8681248	CMK	blood:	n/a
41	chr8:8679450-8679500	K562	blood:	n/a
42	chr8:8680924-8680974	IMR90	lung:	fetal
43	chr8:8681339-8681389	AG04450	lung:	fetal
44	chr8:8681198-8681248	HCPEpiC	choroid plexus:	n/a
45	chr8:8680924-8680974	HEK293	kidney:	embryo
46	chr8:8680971-8681021	AG04449	skin:	fetal
47	chr8:8702053-8702103	AG10803	skin:	n/a
48	chr8:8680971-8681021	NHBE	bronchial:	n/a
49	chr8:8702053-8702103	SKMC	muscle:	n/a
50	chr8:8680924-8680974	HL-60	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8695643..8697451-chr8:8700817..8702338,2	MCF-7	breast:
2	chr8:8676467..8679551-chr8:8749550..8751180,3	K562	blood:
3	chr8:8680684..8683788-chr8:8684972..8687852,3	K562	blood:
4	chr8:8688879..8690529-chr8:8692195..8695178,2	K562	blood:
5	chr8:8665098..8666635-chr8:8667278..8670220,2	MCF-7	breast:
6	chr8:8707079..8709143-chr8:8751442..8753018,2	MCF-7	breast:
7	chr8:8685713..8688062-chr8:8693014..8695350,2	K562	blood:
8	chr8:8702216..8704089-chr8:8704217..8706450,3	K562	blood:
9	chr8:8667410..8669876-chr8:8671325..8673532,2	K562	blood:
10	chr8:8685713..8688062-chr8:8693014..8695350,2	K562	blood:
11	chr8:8700876..8702998-chr8:8749130..8751799,2	MCF-7	breast:
12	chr8:8702216..8704089-chr8:8704217..8706450,3	K562	blood:
13	chr8:8705274..8707873-chr8:8797138..8799236,2	K562	blood:
14	chr8:8672193..8674340-chr8:8678508..8680939,2	K562	blood:
15	chr8:8688879..8690529-chr8:8692195..8695178,2	K562	blood:
16	chr8:8680684..8683788-chr8:8684972..8687852,3	K562	blood:
17	chr8:8669602..8671376-chr8:8685847..8687587,2	K562	blood:
18	chr8:8690681..8693173-chr8:8702089..8703698,2	K562	blood:
19	chr8:8701145..8703921-chr8:8717164..8719093,2	K562	blood:
20	chr8:8667410..8669876-chr8:8671325..8673532,2	K562	blood:
21	chr8:8695643..8697451-chr8:8700817..8702338,2	MCF-7	breast:
22	chr8:8678976..8682016-chr8:8748981..8752043,3	MCF-7	breast:
23	chr8:8669602..8671376-chr8:8685847..8687587,2	K562	blood:
24	chr8:8690681..8693173-chr8:8702089..8703698,2	K562	blood:
25	chr8:8674703..8676330-chr8:8678081..8680231,2	K562	blood:

No data

Variant related genes	Relation type
MFHAS1	TF binding region
MFHAS1	CpG island
ENSG00000147324	chromatin interactions

Extended variants
information (count: 2251 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:2251 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10503390	chr8:8669622-8669623	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113996481	chr8:8669640-8669641	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555149467	chr8:8669681-8669682	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34087173	chr8:8669682-8669683	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs57494325	chr8:8669684-8669685	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571961911	chr8:8669692-8669693	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550753706	chr8:8669697-8669698	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554100737	chr8:8669698-8669699	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527475239	chr8:8669715-8669716	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577152052	chr8:8669729-8669730	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570357404	chr8:8669737-8669738	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546226395	chr8:8669756-8669757	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs17154792	chr8:8669758-8669759	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs576619522	chr8:8669762-8669763	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546521178	chr8:8669767-8669768	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542395416	chr8:8669789-8669790	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112062905	chr8:8669803-8669804	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562292114	chr8:8669812-8669813	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143151926	chr8:8669868-8669869	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148241947	chr8:8669875-8669876	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs114256796	chr8:8669890-8669891	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532785781	chr8:8669912-8669913	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549787288	chr8:8669925-8669926	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs28478802	chr8:8669945-8669946	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs535178231	chr8:8669954-8669955	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs4840362	chr8:8670082-8670083	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs28609361	chr8:8670095-8670096	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182298517	chr8:8670108-8670109	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141665629	chr8:8670126-8670127	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577909919	chr8:8670128-8670129	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146219524	chr8:8670143-8670144	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369486515	chr8:8670162-8670163	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556525316	chr8:8670163-8670164	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7823757	chr8:8670177-8670178	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs111632606	chr8:8670241-8670242	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562199699	chr8:8670261-8670262	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572657215	chr8:8670278-8670279	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541654541	chr8:8670294-8670295	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs60073172	chr8:8670323-8670324	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs398095591	chr8:8670324-8670325	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564613193	chr8:8670330-8670331	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185505481	chr8:8670379-8670380	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10090997	chr8:8670380-8670381	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549461562	chr8:8670384-8670385	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563316733	chr8:8670420-8670421	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370893022	chr8:8670422-8670423	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375606695	chr8:8670428-8670429	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191010953	chr8:8670463-8670464	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548651042	chr8:8670465-8670466	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565465299	chr8:8670466-8670467	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
abnormal development	18461090	CNVD
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
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:1027 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8637600-8679800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:8653800-8674800	Weak transcription	Brain Germinal Matrix	brain
3	chr8:8654000-8671000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr8:8655200-8680600	Weak transcription	Colonic Mucosa	Colon
5	chr8:8655600-8673400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:8655600-8685600	Weak transcription	Fetal Brain Female	brain
7	chr8:8658400-8675200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr8:8658400-8687200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr8:8659400-8671600	Weak transcription	Fetal Muscle Trunk	muscle
10	chr8:8660200-8684400	Weak transcription	HSMMtube	muscle
11	chr8:8662600-8683400	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr8:8662800-8679800	Weak transcription	Brain Angular Gyrus	brain
13	chr8:8663400-8691800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:8663600-8681400	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr8:8664000-8673600	Weak transcription	Stomach Mucosa	stomach
16	chr8:8664000-8678600	Weak transcription	Spleen	Spleen
17	chr8:8664000-8682400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr8:8664200-8675000	Weak transcription	Hela-S3	cervix
19	chr8:8664200-8681200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:8664200-8691400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:8664400-8675200	Weak transcription	Pancreas	Pancrea
22	chr8:8664400-8691800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:8664600-8683200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr8:8665000-8670000	Enhancers	Fetal Lung	lung
25	chr8:8665400-8670800	Enhancers	Colon Smooth Muscle	Colon
26	chr8:8665600-8670000	Enhancers	Lung	lung
27	chr8:8667000-8673200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:8667000-8680000	Weak transcription	Esophagus	oesophagus
29	chr8:8667200-8675000	Weak transcription	Gastric	stomach
30	chr8:8667200-8678400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr8:8667200-8683600	Weak transcription	NHDF-Ad	bronchial
32	chr8:8667200-8685800	Weak transcription	Right Atrium	heart
33	chr8:8667200-8686200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:8667200-8699200	Weak transcription	Aorta	Aorta
35	chr8:8667200-8701600	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr8:8667400-8672400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr8:8667400-8677800	Weak transcription	Fetal Muscle Leg	muscle
38	chr8:8667400-8678200	Weak transcription	Adipose Nuclei	Adipose
39	chr8:8667400-8678400	Weak transcription	A549	lung
40	chr8:8667400-8679000	Weak transcription	NHLF	lung
41	chr8:8667400-8685400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr8:8667400-8686000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:8667400-8693400	Weak transcription	Small Intestine	intestine
44	chr8:8667600-8679200	Weak transcription	HepG2	liver
45	chr8:8667600-8679400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr8:8667600-8679800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:8667600-8685800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr8:8667600-8701000	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr8:8668000-8670600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:8668000-8671800	Weak transcription	Primary B cells from peripheral blood	blood

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