Variant report

Variant	nsv831461
Chromosome Location	chr8:131159819-131302900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2239)
CpG islands
(count:1038)
Chromatin interactive
region (count:80)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2239 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:131299260-131299580	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:131206692-131207309	K562	blood:	n/a	n/a
3	ARID3A	chr8:131206132-131206486	K562	blood:	n/a	n/a
4	ARID3A	chr8:131269153-131269889	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:131219841-131220270	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:131260895-131260909	K562	blood:	n/a	n/a
7	ARID3A	chr8:131218686-131218946	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:131291292-131291998	HepG2	liver:	n/a	n/a
9	ATF1	chr8:131260777-131261117	K562	blood:	n/a	n/a
10	ATF1	chr8:131277086-131277192	K562	blood:	n/a	n/a
11	ATF1	chr8:131251717-131251851	K562	blood:	n/a	n/a
12	ATF1	chr8:131276019-131276310	K562	blood:	n/a	n/a
13	ATF1	chr8:131206964-131207216	K562	blood:	n/a	n/a
14	ATF1	chr8:131296674-131297287	K562	blood:	n/a	n/a
15	ATF1	chr8:131219828-131220171	K562	blood:	n/a	n/a
16	ATF2	chr8:131291093-131291706	GM12878	blood:	n/a	n/a
17	ATF2	chr8:131296785-131297341	GM12878	blood:	n/a	n/a
18	ATF2	chr8:131296765-131297384	GM12878	blood:	n/a	n/a
19	ATF2	chr8:131259661-131260445	GM12878	blood:	n/a	n/a
20	ATF2	chr8:131291064-131291638	GM12878	blood:	n/a	n/a
21	ATF2	chr8:131170715-131171098	GM12878	blood:	n/a	n/a
22	ATF2	chr8:131257080-131257637	GM12878	blood:	n/a	n/a
23	ATF3	chr8:131274835-131275476	HCT-116	colon:	n/a	n/a
24	ATF3	chr8:131206880-131207237	K562	blood:	n/a	n/a
25	ATF3	chr8:131274916-131275631	A549	lung:	n/a	n/a
26	BACH1	chr8:131206920-131207271	K562	blood:	n/a	n/a
27	BACH1	chr8:131206913-131207252	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr8:131269342-131269719	GM12878	blood:	n/a	n/a
29	BATF	chr8:131257157-131257544	GM12878	blood:	n/a	n/a
30	BATF	chr8:131259836-131260188	GM12878	blood:	n/a	n/a
31	BATF	chr8:131296995-131297289	GM12878	blood:	n/a	n/a
32	BATF	chr8:131271654-131271916	GM12878	blood:	n/a	n/a
33	BATF	chr8:131291113-131291713	GM12878	blood:	n/a	n/a
34	BATF	chr8:131257055-131257520	GM12878	blood:	n/a	n/a
35	BATF	chr8:131232951-131233228	GM12878	blood:	n/a	chr8:131233090-131233101
36	BATF	chr8:131271576-131271995	GM12878	blood:	n/a	n/a
37	BATF	chr8:131296763-131296990	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:131296982-131297379	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:131259837-131260214	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:131257168-131257444	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:131259882-131260203	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:131297047-131297362	GM12878	blood:	n/a	n/a
43	BCL3	chr8:131206879-131207253	GM12878	blood:	n/a	n/a
44	BCL3	chr8:131257105-131257595	GM12878	blood:	n/a	n/a
45	BCL3	chr8:131206794-131207275	GM12878	blood:	n/a	n/a
46	BCL3	chr8:131167540-131167867	GM12878	blood:	n/a	n/a
47	BCL3	chr8:131296815-131297308	GM12878	blood:	n/a	n/a
48	BCL3	chr8:131259831-131260211	GM12878	blood:	n/a	n/a
49	BCLAF1	chr8:131257060-131257655	GM12878	blood:	n/a	n/a
50	BCLAF1	chr8:131259742-131260345	GM12878	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:131256328-131256378	ProgFib	skin:	n/a
2	chr8:131256328-131256378	ProgFib	skin:	n/a
3	chr8:131280828-131280878	GM12892	blood:	n/a
4	chr8:131271127-131271177	HEEpiC	esophagus:	n/a
5	chr8:131256328-131256378	NB4	blood:	n/a
6	chr8:131289180-131289230	Hela-S3	cervix:	n/a
7	chr8:131234799-131234849	SK-N-SH_RA	brain:	n/a
8	chr8:131220937-131220987	NHBE	bronchial:	n/a
9	chr8:131220937-131220987	HCPEpiC	choroid plexus:	n/a
10	chr8:131220937-131220987	MCF10A-Er-Src	breast:	n/a
11	chr8:131267301-131267351	SAEC	small airway:	n/a
12	chr8:131256328-131256378	CMK	blood:	n/a
13	chr8:131267301-131267351	PFSK-1	brain:	n/a
14	chr8:131272997-131273047	HepG2	liver:	n/a
15	chr8:131271127-131271177	HCF	heart:	n/a
16	chr8:131213177-131213227	SK-N-SH	brain:	n/a
17	chr8:131217021-131217071	ovcar-3	ovarian:	n/a
18	chr8:131265658-131265708	HRPEpiC	eye:	n/a
19	chr8:131268256-131268306	AG04449	skin:	fetal
20	chr8:131234799-131234849	PANC-1	pancreas:	n/a
21	chr8:131268256-131268306	IMR90	lung:	fetal
22	chr8:131162292-131162342	Jurkat	blood:	n/a
23	chr8:131234799-131234849	A549	lung:	n/a
24	chr8:131272997-131273047	NB4	blood:	n/a
25	chr8:131256328-131256378	GM12892	blood:	n/a
26	chr8:131276557-131276607	NT2-D1	testis:	n/a
27	chr8:131267301-131267351	HCT-116	colon:	n/a
28	chr8:131289180-131289230	BJ	skin:	n/a
29	chr8:131268256-131268306	RPTEC	kidney:	n/a
30	chr8:131265658-131265708	HMEC	breast:	n/a
31	chr8:131234799-131234849	T-47D	breast:	n/a
32	chr8:131267301-131267351	K562	blood:	n/a
33	chr8:131244107-131244157	PrEC	prostate:	n/a
34	chr8:131289180-131289230	HNPCEpiC	eye:	n/a
35	chr8:131244107-131244157	IMR90	lung:	fetal
36	chr8:131250320-131250370	HCT-116	colon:	n/a
37	chr8:131256328-131256378	AG04449	skin:	fetal
38	chr8:131289180-131289230	AoSMC	blood vessel:	n/a
39	chr8:131267301-131267351	Hepatocyte	liver:	n/a
40	chr8:131265658-131265708	CMK	blood:	n/a
41	chr8:131162292-131162342	AG04449	skin:	fetal
42	chr8:131280828-131280878	AG04450	lung:	fetal
43	chr8:131213177-131213227	ECC-1	luminal epithelium:	n/a
44	chr8:131220937-131220987	ovcar-3	ovarian:	n/a
45	chr8:131267301-131267351	HRCEpiC	kidney:	n/a
46	chr8:131276557-131276607	HCF	heart:	n/a
47	chr8:131162292-131162342	NH-A	brain:	n/a
48	chr8:131268256-131268306	T-47D	breast:	n/a
49	chr8:131300227-131300277	NB4	blood:	n/a
50	chr8:131217021-131217071	IMR90	lung:	fetal

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:131187972..131189783-chr8:131206468..131207978,2	K562	blood:
2	chr8:131263978..131265844-chr8:131269482..131272106,2	MCF-7	breast:
3	chr8:131249163..131251743-chr8:131252755..131255422,3	K562	blood:
4	chr8:131214869..131216491-chr8:131224118..131225672,2	K562	blood:
5	chr8:131219609..131220494-chr8:131428490..131429541,6	MCF-7	breast:
6	chr8:131190104..131192008-chr8:131192113..131194046,2	MCF-7	breast:
7	chr8:131295924..131298030-chr8:131301524..131303913,2	K562	blood:
8	chr8:131192568..131195511-chr8:131198204..131200950,2	K562	blood:
9	chr8:131290504..131292018-chr8:131292531..131294488,2	MCF-7	breast:
10	chr8:131192568..131194761-chr8:131198204..131200041,2	K562	blood:
11	chr8:131274673..131277177-chr8:131288915..131291694,2	K562	blood:
12	chr8:131302789..131304679-chr8:131308821..131310748,2	MCF-7	breast:
13	chr8:131207362..131209756-chr8:131210863..131213512,2	MCF-7	breast:
14	chr8:131251770..131253963-chr8:131254539..131258197,4	K562	blood:
15	chr8:131182729..131185672-chr8:131189241..131191289,2	K562	blood:
16	chr8:131234063..131236544-chr8:131237880..131240227,2	K562	blood:
17	chr8:131214869..131216491-chr8:131224118..131225672,2	K562	blood:
18	chr8:131230566..131233356-chr8:131236600..131238831,2	MCF-7	breast:
19	chr8:131277435..131279896-chr8:131293652..131295449,2	K562	blood:
20	chr8:131216012..131218539-chr8:131221630..131223240,2	K562	blood:
21	chr8:131196822..131199241-chr8:131335887..131338128,2	K562	blood:
22	chr8:131277435..131279896-chr8:131293652..131295449,2	K562	blood:
23	chr8:131213858..131216105-chr8:131217868..131219990,3	K562	blood:
24	chr8:131276192..131278199-chr8:131282560..131285411,2	MCF-7	breast:
25	chr8:131166087..131168835-chr8:131177427..131180204,2	K562	blood:
26	chr8:131283513..131285775-chr8:131309239..131311287,2	K562	blood:
27	chr5:10489698..10490407-chr8:131234346..131235296,2	MCF-7	breast:
28	chr8:131279813..131282288-chr8:131286775..131289036,2	MCF-7	breast:
29	chr8:131267673..131269776-chr8:131275129..131276905,2	K562	blood:
30	chr8:131281505..131283976-chr8:131286919..131289472,2	K562	blood:
31	chr8:131187972..131189783-chr8:131206468..131207978,2	K562	blood:
32	chr8:131295924..131298030-chr8:131301524..131303913,2	K562	blood:
33	chr8:131178586..131180202-chr8:131182476..131184187,2	K562	blood:
34	chr8:131273772..131275744-chr8:131368224..131371036,2	MCF-7	breast:
35	chr8:131296841..131298390-chr8:131305321..131307760,2	K562	blood:
36	chr8:131261093..131263625-chr8:131272270..131274011,4	K562	blood:
37	chr8:131279813..131282288-chr8:131286775..131289036,2	MCF-7	breast:
38	chr8:131194316..131196588-chr8:131199772..131201320,2	MCF-7	breast:
39	chr8:131256131..131258801-chr8:131266345..131268864,3	MCF-7	breast:
40	chr8:131219895..131220464-chr8:131663009..131663552,2	MCF-7	breast:
41	chr8:131281505..131283976-chr8:131286919..131289472,2	K562	blood:
42	chr8:131290504..131292018-chr8:131292531..131294488,2	MCF-7	breast:
43	chr8:131219943..131220583-chr8:131688855..131689396,2	MCF-7	breast:
44	chr8:131274673..131277177-chr8:131288915..131291694,2	K562	blood:
45	chr8:131248177..131251227-chr8:131256554..131258838,3	MCF-7	breast:
46	chr8:131278240..131280307-chr8:131313127..131315525,2	K562	blood:
47	chr8:131178586..131180202-chr8:131182476..131184187,2	K562	blood:
48	chr8:131276192..131278199-chr8:131282560..131285411,2	MCF-7	breast:
49	chr8:131224006..131226122-chr8:131244527..131247390,2	K562	blood:
50	chr8:131236220..131238731-chr8:131241044..131243639,2	MCF-7	breast:

No data

Variant related genes	Relation type
ASAP1	TF binding region
ENSG00000212342	TF binding region
ASAP1	CpG island
ENSG00000212342	CpG island
ENSG00000153317	chromatin interactions

Extended variants
information (count: 5363 )
Associated
traits (count: 158 )

Variant overlapped rSNPs/rCNVs (count:5363 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75935546	chr8:131159849-131159850	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs77072400	chr8:131159875-131159876	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76705697	chr8:131159917-131159918	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4733771	chr8:131159927-131159928	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs72722355	chr8:131159933-131159934	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs193151825	chr8:131159969-131159970	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374908183	chr8:131159982-131159983	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183166265	chr8:131160146-131160147	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568214658	chr8:131160149-131160150	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575054259	chr8:131160153-131160154	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542809596	chr8:131160192-131160193	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554724129	chr8:131160228-131160229	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560817763	chr8:131160236-131160237	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528229847	chr8:131160281-131160282	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186779285	chr8:131160284-131160285	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577105657	chr8:131160289-131160290	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191146814	chr8:131160326-131160327	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532167780	chr8:131160338-131160339	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551263006	chr8:131160378-131160379	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369578516	chr8:131160421-131160422	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184070294	chr8:131160447-131160448	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs55705977	chr8:131160456-131160457	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs199704701	chr8:131160468-131160469	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199577556	chr8:131160476-131160477	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566845588	chr8:131160489-131160490	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73712881	chr8:131160539-131160540	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs558803373	chr8:131160546-131160547	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375816805	chr8:131160549-131160550	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142116281	chr8:131160561-131160562	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371750033	chr8:131160606-131160607	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188360397	chr8:131160634-131160635	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146662581	chr8:131160654-131160655	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542447841	chr8:131160665-131160666	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193163964	chr8:131160670-131160671	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185324231	chr8:131160681-131160682	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369244273	chr8:131160732-131160733	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572829449	chr8:131160744-131160745	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563860691	chr8:131160774-131160775	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540297396	chr8:131160789-131160790	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564989951	chr8:131160836-131160837	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532106464	chr8:131160938-131160939	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190224512	chr8:131160947-131160948	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182222227	chr8:131160964-131160965	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372670447	chr8:131161024-131161025	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563175105	chr8:131161084-131161085	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199811164	chr8:131161087-131161088	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140252753	chr8:131161093-131161094	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548470347	chr8:131161106-131161107	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567023537	chr8:131161108-131161109	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12678316	chr8:131161125-131161126	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:158)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Osteosarcoma	21215367	CNVD
Cancer	20164919	CNVD

Chromatin state (count:5124 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131076200-131170600	Weak transcription	Small Intestine	intestine
2	chr8:131116000-131193800	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr8:131128800-131186800	Weak transcription	Fetal Brain Male	brain
4	chr8:131130400-131180200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr8:131138800-131164600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr8:131140000-131169200	Weak transcription	Brain Angular Gyrus	brain
7	chr8:131141400-131164400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr8:131146600-131178800	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr8:131146600-131206000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:131147200-131163800	Weak transcription	Colon Smooth Muscle	Colon
11	chr8:131147400-131194400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr8:131147600-131162000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:131147600-131170400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr8:131147600-131199800	Weak transcription	Pancreas	Pancrea
15	chr8:131148000-131183800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr8:131148000-131194400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr8:131148400-131169800	Weak transcription	K562	blood
18	chr8:131148600-131164800	Weak transcription	Brain Anterior Caudate	brain
19	chr8:131148600-131169800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:131148600-131170200	Weak transcription	Fetal Intestine Small	intestine
21	chr8:131149000-131162000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr8:131149000-131168000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr8:131149000-131170600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr8:131149000-131178400	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr8:131149200-131162200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr8:131149200-131163600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr8:131149200-131163600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr8:131149200-131163800	Weak transcription	Brain Hippocampus Middle	brain
29	chr8:131149200-131164000	Weak transcription	Brain Substantia Nigra	brain
30	chr8:131149200-131168600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr8:131149200-131172200	Weak transcription	HepG2	liver
32	chr8:131149200-131178600	Weak transcription	Brain Cingulate Gyrus	brain
33	chr8:131149200-131184400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr8:131149400-131161800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr8:131149400-131163800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr8:131149400-131163800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr8:131149400-131169200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr8:131149400-131169600	Weak transcription	Rectal Smooth Muscle	rectum
39	chr8:131149600-131162200	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr8:131149600-131169400	Weak transcription	Thymus	Thymus
41	chr8:131150200-131160000	Weak transcription	Fetal Brain Female	brain
42	chr8:131150200-131168600	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr8:131150600-131162000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:131150800-131160200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr8:131150800-131169600	Weak transcription	Brain Germinal Matrix	brain
46	chr8:131152000-131181000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr8:131152200-131182200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:131152800-131193600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr8:131154400-131164600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr8:131155000-131168600	Weak transcription	Esophagus	oesophagus

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