Variant report

Variant	nsv916493
Chromosome Location	chr8:9806580-10029482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1824)
CpG islands
(count:2259)
Chromatin interactive
region (count:64)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1824 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:9899121-9899480	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:9807513-9807613	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:10009672-10010165	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:9899228-9899452	K562	blood:	n/a	n/a
5	ARID3A	chr8:10009586-10009863	K562	blood:	n/a	n/a
6	ATF2	chr8:9912232-9913171	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:9911951-9912524	GM12878	blood:	n/a	n/a
8	ATF2	chr8:9820970-9821460	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr8:9912053-9912316	K562	blood:	n/a	n/a
10	BACH1	chr8:9953856-9953925	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:9912069-9913020	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:10009852-10010062	H1-hESC	embryonic stem cell:	n/a	chr8:10009959-10009973
13	BACH1	chr8:9988646-9988815	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:9916888-9917068	K562	blood:	n/a	n/a
15	BACH1	chr8:10016151-10016334	K562	blood:	n/a	n/a
16	BACH1	chr8:9899213-9899384	K562	blood:	n/a	n/a
17	BATF	chr8:9944587-9944852	GM12878	blood:	n/a	chr8:9944757-9944768
18	BCL11A	chr8:9911989-9912292	GM12878	blood:	n/a	chr8:9912225-9912238
19	BCL3	chr8:9918619-9918855	GM12878	blood:	n/a	n/a
20	BCL3	chr8:9918552-9919122	GM12878	blood:	n/a	n/a
21	BCL3	chr8:9912194-9912635	A549	lung:	n/a	chr8:9912225-9912238 chr8:9912550-9912563
22	BCL3	chr8:10009722-10010009	GM12878	blood:	n/a	n/a
23	BCL3	chr8:10023733-10024165	GM12878	blood:	n/a	n/a
24	BCL3	chr8:10002131-10002433	GM12878	blood:	n/a	n/a
25	BCL3	chr8:9919920-9920213	GM12878	blood:	n/a	n/a
26	BCL3	chr8:9918857-9919252	GM12878	blood:	n/a	n/a
27	BCLAF1	chr8:9911393-9912622	GM12878	blood:	n/a	chr8:9912225-9912238 chr8:9912550-9912563
28	BHLHE40	chr8:9951335-9951662	K562	blood:	n/a	n/a
29	BHLHE40	chr8:9911642-9911834	K562	blood:	n/a	n/a
30	BHLHE40	chr8:9911564-9911707	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:9951338-9951626	HepG2	liver:	n/a	n/a
32	BHLHE40	chr8:9912102-9912808	K562	blood:	n/a	chr8:9912727-9912743 chr8:9912550-9912566
33	BHLHE40	chr8:9951404-9951632	A549	lung:	n/a	n/a
34	BHLHE40	chr8:9857183-9857387	K562	blood:	n/a	n/a
35	BHLHE40	chr8:9966233-9966301	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:9857207-9857384	HepG2	liver:	n/a	n/a
37	BHLHE40	chr8:9912026-9913041	GM12878	blood:	n/a	chr8:9912727-9912743 chr8:9912550-9912566
38	BHLHE40	chr8:9956535-9956793	K562	blood:	n/a	chr8:9956727-9956736 chr8:9956721-9956742 chr8:9956727-9956736 chr8:9956726-9956735 chr8:9956725-9956738
39	BHLHE40	chr8:9951427-9951617	GM12878	blood:	n/a	n/a
40	BRCA1	chr8:10009571-10010154	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr8:9915042-9915339	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr8:9911491-9911711	HepG2	liver:	n/a	n/a
43	BRCA1	chr8:9912182-9912551	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr8:9911604-9911835	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr8:9947190-9947939	HCT-116	colon:	n/a	chr8:9947671-9947682
46	CBX3	chr8:9947154-9947974	HCT-116	colon:	n/a	chr8:9947671-9947682
47	CBX3	chr8:9951179-9951780	HCT-116	colon:	n/a	n/a
48	CBX3	chr8:9944287-9945283	HCT-116	colon:	n/a	n/a
49	CBX3	chr8:9807417-9807737	K562	blood:	n/a	n/a
50	CBX3	chr8:10009275-10010611	HCT-116	colon:	n/a	n/a

(count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9911630-9911680	SKMC	muscle:	n/a
2	chr8:10005423-10005473	T-47D	breast:	n/a
3	chr8:9911630-9911680	SKMC	muscle:	n/a
4	chr8:10005423-10005473	T-47D	breast:	n/a
5	chr8:10005474-10005524	ECC-1	luminal epithelium:	n/a
6	chr8:9911636-9911686	PANC-1	pancreas:	n/a
7	chr8:9913680-9913730	LNCaP	prostate:	n/a
8	chr8:9987847-9987897	GM12878	blood:	n/a
9	chr8:9911669-9911719	PrEC	prostate:	n/a
10	chr8:9913680-9913730	AG04450	lung:	fetal
11	chr8:9911765-9911815	BE2_C	brain:	n/a
12	chr8:10005474-10005524	HCM	heart:	n/a
13	chr8:9911669-9911719	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:9912509-9912559	PANC-1	pancreas:	n/a
15	chr8:9911669-9911719	SK-N-SH	brain:	n/a
16	chr8:9911765-9911815	K562	blood:	n/a
17	chr8:10001627-10001677	ProgFib	skin:	n/a
18	chr8:9952636-9952686	HUVEC	blood vessel:	n/a
19	chr8:9870454-9870504	HepG2	liver:	n/a
20	chr8:9912632-9912682	HUVEC	blood vessel:	n/a
21	chr8:9912305-9912355	HCF	heart:	n/a
22	chr8:9911685-9911735	GM12878	blood:	n/a
23	chr8:9953022-9953072	HEK293	kidney:	embryo
24	chr8:9947360-9947410	ECC-1	luminal epithelium:	n/a
25	chr8:9842043-9842093	NT2-D1	testis:	n/a
26	chr8:9951983-9952033	SK-N-SH_RA	brain:	n/a
27	chr8:10005474-10005524	RPTEC	kidney:	n/a
28	chr8:9911765-9911815	NHBE	bronchial:	n/a
29	chr8:9911988-9912038	U87	brain:	n/a
30	chr8:9911641-9911691	GM06990	blood:	n/a
31	chr8:9913680-9913730	HepG2	liver:	n/a
32	chr8:9952636-9952686	U87	brain:	n/a
33	chr8:9952636-9952686	PFSK-1	brain:	n/a
34	chr8:9912981-9913031	NHBE	bronchial:	n/a
35	chr8:9912509-9912559	ECC-1	luminal epithelium:	n/a
36	chr8:10001523-10001573	U87	brain:	n/a
37	chr8:9870454-9870504	RPTEC	kidney:	n/a
38	chr8:9912509-9912559	NHDF-neo	bronchial:	n/a
39	chr8:10005474-10005524	HPAEpiC	pulmonary alveolar:	n/a
40	chr8:9912509-9912559	HEEpiC	esophagus:	n/a
41	chr8:9912509-9912559	NT2-D1	testis:	n/a
42	chr8:10005423-10005473	HCT-116	colon:	n/a
43	chr8:9913680-9913730	ProgFib	skin:	n/a
44	chr8:9911641-9911691	GM12878	blood:	n/a
45	chr8:9953022-9953072	Hepatocyte	liver:	n/a
46	chr8:9912981-9913031	AoSMC	blood vessel:	n/a
47	chr8:9965554-9965604	MCF-7	breast:	n/a
48	chr8:9911760-9911810	NT2-D1	testis:	n/a
49	chr8:9911669-9911719	GM06990	blood:	n/a
50	chr8:9952926-9952976	LNCaP	prostate:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:9922401..9925276-chr8:9927824..9930255,2	K562	blood:
2	chr8:9918343..9921337-chr8:9921540..9924718,3	K562	blood:
3	chr3:149530376..149530908-chr8:9911845..9912431,2	HCT-116	colon:
4	chr8:9891135..9893844-chr8:9895731..9897309,2	K562	blood:
5	chr8:9968733..9972257-chr8:9973876..9975676,3	K562	blood:
6	chr8:9918343..9921337-chr8:9921540..9924718,3	K562	blood:
7	chr8:9815054..9815608-chr8:10190020..10190697,2	MCF-7	breast:
8	chr8:9910777..9912807-chr8:10008037..10009823,2	MCF-7	breast:
9	chr8:9912174..9913822-chr8:9921464..9923860,2	K562	blood:
10	chr8:9985280..9987758-chr8:9989379..9992085,2	K562	blood:
11	chr8:9912450..9914254-chr8:9914390..9916277,2	MCF-7	breast:
12	chr8:9919631..9921337-chr8:9921540..9924138,2	K562	blood:
13	chr8:9963502..9966052-chr8:9972558..9974638,2	MCF-7	breast:
14	chr8:9912174..9913822-chr8:9921464..9923860,2	K562	blood:
15	chr8:9930550..9933030-chr8:9938731..9941412,2	K562	blood:
16	chr8:9907816..9909322-chr8:9909442..9912164,2	MCF-7	breast:
17	chr8:9803039..9805546-chr8:9809803..9812661,2	K562	blood:
18	chr8:9898731..9899394-chr8:10399301..10400191,2	MCF-7	breast:
19	chr8:9891135..9893844-chr8:9895731..9897309,2	K562	blood:
20	chr8:9989052..9991739-chr8:9991879..9993683,2	K562	blood:
21	chr8:9815524..9816032-chr8:10190161..10190769,2	MCF-7	breast:
22	chr8:9911649..9914340-chr8:9934101..9935936,2	MCF-7	breast:
23	chr8:9839190..9841149-chr8:9843519..9845588,2	K562	blood:
24	chr8:9903435..9909004-chr8:9909616..9914452,5	K562	blood:
25	chr8:9898835..9899700-chr8:10131105..10131973,4	MCF-7	breast:
26	chr8:9912450..9914254-chr8:9914390..9916277,2	MCF-7	breast:
27	chr8:9839190..9841149-chr8:9843519..9845588,2	K562	blood:
28	chr8:9902844..9907723-chr8:9908592..9913674,8	MCF-7	breast:
29	chr8:9959952..9962225-chr8:9964575..9967404,2	MCF-7	breast:
30	chr8:9954771..9956774-chr8:9960148..9962685,2	K562	blood:
31	chr8:9922401..9925276-chr8:9927824..9930255,2	K562	blood:
32	chr8:9951257..9953099-chr8:9953951..9956586,3	MCF-7	breast:
33	chr8:9968733..9972257-chr8:9973876..9975676,3	K562	blood:
34	chr8:9911713..9914298-chr8:9916652..9919160,3	MCF-7	breast:
35	chr8:9985940..9988660-chr8:9990986..9993361,2	K562	blood:
36	chr8:9985280..9987758-chr8:9989379..9992085,2	K562	blood:
37	chr8:9911742..9913347-chr8:9941855..9944442,2	K562	blood:
38	chr8:9898892..9899783-chr8:10131113..10132044,4	K562	blood:
39	chr8:9954771..9956774-chr8:9960148..9962685,2	K562	blood:
40	chr17:79825287..79825828-chr8:9912227..9912805,2	HCT-116	colon:
41	chr13:52158355..52159026-chr8:9911353..9912342,2	NB4	blood:
42	chr8:9963502..9966052-chr8:9972558..9974638,2	MCF-7	breast:
43	chr8:9898822..9899498-chr8:10190113..10190904,3	K562	blood:
44	chr8:9985940..9988660-chr8:9990986..9993361,2	K562	blood:
45	chr8:9930550..9933030-chr8:9938731..9941412,2	K562	blood:
46	chr8:9898874..9899812-chr8:10282419..10282930,2	K562	blood:
47	chr8:9803809..9806790-chr8:9814739..9816727,2	K562	blood:
48	chr8:9859284..9862073-chr8:9868514..9870369,2	K562	blood:
49	chr8:9823483..9825109-chr8:9827263..9829750,2	K562	blood:
50	chr8:9803809..9806790-chr8:9814739..9816727,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP1L1-4	chr8:9895361-9895841	XLOC_007003
2	lnc-RP1L1-4	chr8:9909270-9909473	XLOC_007003

No data

Variant related genes	Relation type
MSRA	TF binding region
ENSG00000260093	TF binding region
ENSG00000221320	TF binding region
MSRA	CpG island
ENSG00000260093	CpG island
ENSG00000221320	CpG island
ENSG00000104635	chromatin interactions
ENSG00000205352	chromatin interactions
ENSG00000260093	chromatin interactions
ENSG00000175806	chromatin interactions
ENSG00000262413	chromatin interactions
ENSG00000139668	chromatin interactions
ENSG00000197111	chromatin interactions
ENSG00000082996	chromatin interactions
PTP4A1	miRNA target sites

Extended variants
information (count: 10412 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:10412 , 50 per page) page: 1 2 3 4 5 6 7 ... 209

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184753196	chr8:9807212-9807213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540452816	chr8:9807216-9807217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569730481	chr8:9807217-9807218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560169235	chr8:9807246-9807247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs367912545	chr8:9807264-9807265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577118690	chr8:9807299-9807300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188643731	chr8:9807315-9807316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562514907	chr8:9807331-9807332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531259806	chr8:9807334-9807335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573899426	chr8:9807356-9807357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561112624	chr8:9807366-9807367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180691726	chr8:9807391-9807392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542517646	chr8:9807397-9807398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183753377	chr8:9807457-9807458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562764662	chr8:9807458-9807459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547219015	chr8:9807465-9807466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567043309	chr8:9807489-9807490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189303353	chr8:9807492-9807493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143861416	chr8:9807522-9807523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182488880	chr8:9807530-9807531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538305881	chr8:9807540-9807541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530975201	chr8:9807556-9807557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145860644	chr8:9807565-9807566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575011977	chr8:9807589-9807590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544597896	chr8:9807608-9807609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34653681	chr8:9807634-9807635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369202859	chr8:9807652-9807653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533747264	chr8:9807661-9807662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564604059	chr8:9807678-9807679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369483043	chr8:9807705-9807706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34791768	chr8:9807706-9807707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs59802396	chr8:9807727-9807728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551349250	chr8:9815601-9815602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564895759	chr8:9815651-9815652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113417429	chr8:9815657-9815658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530589310	chr8:9815675-9815676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542664280	chr8:9815678-9815679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147311043	chr8:9815688-9815689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567385227	chr8:9815711-9815712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535669215	chr8:9815715-9815716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549562388	chr8:9815716-9815717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141008932	chr8:9815743-9815744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11283399	chr8:9815758-9815759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141940519	chr8:9815760-9815761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11283389	chr8:9815765-9815766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200330395	chr8:9815766-9815767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535004813	chr8:9815768-9815769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185603366	chr8:9815793-9815794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs189594662	chr8:9815818-9815819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537075152	chr8:9815854-9815855	Enhancers Weak transcription	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
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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Osteosarcoma	21215367	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Renal cell carcinoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1781 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9807200-9807800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:9807400-9807800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:9815600-9815800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr8:9815600-9815800	Enhancers	Fetal Brain Male	brain
5	chr8:9815600-9816000	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:9815800-9818800	Weak transcription	Fetal Brain Male	brain
7	chr8:9818800-9819400	Enhancers	Fetal Brain Male	brain
8	chr8:9819000-9819200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr8:9819000-9819400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr8:9819200-9820400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr8:9819400-9819800	Weak transcription	Fetal Brain Male	brain
12	chr8:9819400-9820800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:9819800-9822400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:9819800-9822800	Enhancers	Fetal Brain Male	brain
15	chr8:9819800-9823000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:9820000-9820800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr8:9820000-9820800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr8:9820000-9822400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:9820000-9823000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr8:9820200-9820400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr8:9820200-9820400	Enhancers	Fetal Brain Female	brain
22	chr8:9820200-9820800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr8:9820200-9821000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr8:9820200-9821000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr8:9820200-9822000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr8:9820400-9820600	Flanking Active TSS	Fetal Brain Female	brain
27	chr8:9820400-9820800	Enhancers	Brain Germinal Matrix	brain
28	chr8:9820400-9820800	Enhancers	Brain Hippocampus Middle	brain
29	chr8:9820400-9821000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr8:9820400-9821800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr8:9820400-9821800	Enhancers	Brain Substantia Nigra	brain
32	chr8:9820400-9822400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr8:9820600-9821000	Active TSS	Fetal Brain Female	brain
34	chr8:9820600-9821800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr8:9820600-9821800	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr8:9820600-9822000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:9820600-9822400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr8:9820800-9821000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr8:9820800-9821000	Bivalent Enhancer	GM12878-XiMat	blood
40	chr8:9820800-9821400	Enhancers	Brain Cingulate Gyrus	brain
41	chr8:9820800-9821600	Flanking Active TSS	Brain Germinal Matrix	brain
42	chr8:9820800-9821800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr8:9820800-9821800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr8:9820800-9821800	Active TSS	Brain Anterior Caudate	brain
45	chr8:9820800-9821800	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr8:9820800-9822000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr8:9820800-9822400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:9821000-9821200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr8:9821000-9821200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr8:9821000-9821200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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