Variant report

Variant	nsv891446
Chromosome Location	chr8:130656205-130710638
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1344)
CpG islands
(count:122)
Chromatin interactive
region (count:78)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:130710276-130710449	K562	blood:	n/a	n/a
2	ARID3A	chr8:130699624-130700115	K562	blood:	n/a	n/a
3	ARID3A	chr8:130704430-130705462	K562	blood:	n/a	n/a
4	ARID3A	chr8:130690024-130690499	K562	blood:	n/a	n/a
5	ARID3A	chr8:130709396-130709681	K562	blood:	n/a	n/a
6	ARID3A	chr8:130694294-130694614	K562	blood:	n/a	n/a
7	ARID3A	chr8:130697568-130697735	K562	blood:	n/a	n/a
8	ARID3A	chr8:130701435-130702061	K562	blood:	n/a	n/a
9	ATF1	chr8:130703204-130703642	K562	blood:	n/a	n/a
10	ATF1	chr8:130701480-130702076	K562	blood:	n/a	n/a
11	ATF1	chr8:130704507-130705519	K562	blood:	n/a	n/a
12	ATF1	chr8:130689997-130690462	K562	blood:	n/a	n/a
13	ATF2	chr8:130688883-130689357	GM12878	blood:	n/a	n/a
14	ATF2	chr8:130688875-130689366	GM12878	blood:	n/a	n/a
15	ATF3	chr8:130697689-130698388	A549	lung:	n/a	n/a
16	ATF3	chr8:130704495-130704908	K562	blood:	n/a	chr8:130704730-130704745 chr8:130704731-130704744
17	ATF3	chr8:130694015-130694732	A549	lung:	n/a	n/a
18	ATF3	chr8:130694100-130694706	A549	lung:	n/a	n/a
19	BACH1	chr8:130695046-130695069	K562	blood:	n/a	n/a
20	BACH1	chr8:130705205-130705279	K562	blood:	n/a	n/a
21	BACH1	chr8:130704245-130704377	K562	blood:	n/a	n/a
22	BCL3	chr8:130693999-130694732	A549	lung:	n/a	n/a
23	BCL3	chr8:130692822-130693174	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:130703163-130703576	K562	blood:	n/a	n/a
25	BHLHE40	chr8:130701543-130702287	K562	blood:	n/a	chr8:130702154-130702175
26	BHLHE40	chr8:130694299-130694629	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:130702575-130702640	K562	blood:	n/a	n/a
28	BHLHE40	chr8:130699755-130700290	K562	blood:	n/a	n/a
29	BHLHE40	chr8:130704462-130705619	K562	blood:	n/a	chr8:130705473-130705489
30	BHLHE40	chr8:130697965-130698035	K562	blood:	n/a	n/a
31	BHLHE40	chr8:130709476-130709820	K562	blood:	n/a	n/a
32	BHLHE40	chr8:130694182-130694597	K562	blood:	n/a	n/a
33	BRCA1	chr8:130694339-130694539	HepG2	liver:	n/a	n/a
34	CBX3	chr8:130710174-130710853	K562	blood:	n/a	n/a
35	CBX3	chr8:130704087-130705480	K562	blood:	n/a	n/a
36	CBX3	chr8:130681478-130682118	K562	blood:	n/a	n/a
37	CBX3	chr8:130709255-130710982	HCT-116	colon:	n/a	n/a
38	CBX3	chr8:130703142-130703662	K562	blood:	n/a	n/a
39	CBX3	chr8:130701308-130702021	K562	blood:	n/a	n/a
40	CBX3	chr8:130659198-130660162	K562	blood:	n/a	n/a
41	CBX3	chr8:130681426-130682331	K562	blood:	n/a	n/a
42	CBX3	chr8:130699588-130700068	K562	blood:	n/a	n/a
43	CBX3	chr8:130680647-130680961	K562	blood:	n/a	n/a
44	CCNT2	chr8:130704626-130705637	K562	blood:	n/a	n/a
45	CCNT2	chr8:130703227-130703528	K562	blood:	n/a	n/a
46	CCNT2	chr8:130694269-130694691	K562	blood:	n/a	n/a
47	CCNT2	chr8:130701341-130702241	K562	blood:	n/a	n/a
48	CCNT2	chr8:130690110-130690468	K562	blood:	n/a	n/a
49	CEBPB	chr8:130704160-130704207	K562	blood:	n/a	n/a
50	CEBPB	chr8:130704946-130705458	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:130691556-130691606	NHBE	bronchial:	n/a
2	chr8:130698161-130698211	T-47D	breast:	n/a
3	chr8:130691556-130691606	SAEC	small airway:	n/a
4	chr8:130691556-130691606	AG09319	gingival:	n/a
5	chr8:130691556-130691606	HNPCEpiC	eye:	n/a
6	chr8:130691556-130691606	NT2-D1	testis:	n/a
7	chr8:130691556-130691606	Hela-S3	cervix:	n/a
8	chr8:130698161-130698211	GM12878	blood:	n/a
9	chr8:130698161-130698211	HepG2	liver:	n/a
10	chr8:130691556-130691606	HL-60	blood:	n/a
11	chr8:130698161-130698211	K562	blood:	n/a
12	chr8:130698161-130698211	AG04449	skin:	fetal
13	chr8:130698161-130698211	SAEC	small airway:	n/a
14	chr8:130698161-130698211	HIPEpiC	eye:	n/a
15	chr8:130691556-130691606	SK-N-SH_RA	brain:	n/a
16	chr8:130691556-130691606	HCT-116	colon:	n/a
17	chr8:130698161-130698211	HNPCEpiC	eye:	n/a
18	chr8:130698161-130698211	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:130698161-130698211	RPTEC	kidney:	n/a
20	chr8:130691556-130691606	HRCEpiC	kidney:	n/a
21	chr8:130698161-130698211	NT2-D1	testis:	n/a
22	chr8:130698161-130698211	ProgFib	skin:	n/a
23	chr8:130691556-130691606	GM12878	blood:	n/a
24	chr8:130698161-130698211	A549	lung:	n/a
25	chr8:130691556-130691606	GM12891	blood:	n/a
26	chr8:130698161-130698211	MCF10A-Er-Src	breast:	n/a
27	chr8:130698161-130698211	HCT-116	colon:	n/a
28	chr8:130691556-130691606	MCF10A-Er-Src	breast:	n/a
29	chr8:130698161-130698211	H1-hESC	embryonic stem cell:	embryo
30	chr8:130691556-130691606	HAEpiC	amniotic membrane:	n/a
31	chr8:130691556-130691606	K562	blood:	n/a
32	chr8:130698161-130698211	BE2_C	brain:	n/a
33	chr8:130698161-130698211	HRPEpiC	eye:	n/a
34	chr8:130691556-130691606	HepG2	liver:	n/a
35	chr8:130691556-130691606	BJ	skin:	n/a
36	chr8:130698161-130698211	HL-60	blood:	n/a
37	chr8:130691556-130691606	Jurkat	blood:	n/a
38	chr8:130698161-130698211	AG09319	gingival:	n/a
39	chr8:130691556-130691606	HCF	heart:	n/a
40	chr8:130698161-130698211	Jurkat	blood:	n/a
41	chr8:130691556-130691606	HEK293	kidney:	embryo
42	chr8:130691556-130691606	CMK	blood:	n/a
43	chr8:130691556-130691606	U87	brain:	n/a
44	chr8:130691556-130691606	HUVEC	blood vessel:	n/a
45	chr8:130691556-130691606	HRE	kidney:	n/a
46	chr8:130698161-130698211	GM12892	blood:	n/a
47	chr8:130691556-130691606	ECC-1	luminal epithelium:	n/a
48	chr8:130691556-130691606	T-47D	breast:	n/a
49	chr8:130691556-130691606	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:130698161-130698211	CMK	blood:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:130709158..130713272-chr8:130716107..130718644,3	K562	blood:
2	chr8:128752824..128755254-chr8:130703895..130705985,2	K562	blood:
3	chr8:130551039..130551980-chr8:130694084..130694624,2	MCF-7	breast:
4	chr8:130696204..130698352-chr8:130701733..130703322,2	K562	blood:
5	chr8:130693914..130694433-chr8:130740865..130741380,2	MCF-7	breast:
6	chr8:128747402..128749351-chr8:130710399..130712084,2	K562	blood:
7	chr8:130688486..130691516-chr8:130701686..130704518,3	K562	blood:
8	chr8:130700584..130702961-chr8:130710020..130711748,2	MCF-7	breast:
9	chr8:128746816..128749956-chr8:130699107..130701261,3	K562	blood:
10	chr8:130689876..130691516-chr8:130698060..130699622,2	K562	blood:
11	chr8:130595446..130597443-chr8:130678886..130681911,3	K562	blood:
12	chr8:130703853..130706502-chr8:130708490..130712451,4	K562	blood:
13	chr8:130699826..130701651-chr8:130708566..130712426,4	K562	blood:
14	chr8:130696204..130698352-chr8:130701733..130703322,2	K562	blood:
15	chr8:130608180..130609853-chr8:130686096..130687708,2	K562	blood:
16	chr8:130699826..130701651-chr8:130708566..130712426,4	K562	blood:
17	chr8:130547962..130549604-chr8:130709178..130711041,2	MCF-7	breast:
18	chr8:130700888..130706431-chr8:130718980..130724092,7	K562	blood:
19	chr8:130698168..130701867-chr8:130706682..130711085,4	MCF-7	breast:
20	chr8:130660996..130663314-chr8:130665198..130667685,2	MCF-7	breast:
21	chr8:130709015..130711494-chr8:130712126..130713771,2	K562	blood:
22	chr8:130585350..130587697-chr8:130704130..130706568,2	K562	blood:
23	chr8:128747945..128750737-chr8:130685939..130690033,4	K562	blood:
24	chr8:130692959..130695780-chr8:130701945..130704433,2	K562	blood:
25	chr8:127881390..127882102-chr8:130693928..130694709,3	K562	blood:
26	chr8:130661192..130664016-chr8:130665123..130667004,3	K562	blood:
27	chr8:130595589..130597194-chr8:130700231..130702653,2	K562	blood:
28	chr8:130709093..130710072-chr8:130738277..130738889,2	MCF-7	breast:
29	chr8:130662457..130664068-chr8:130664538..130667140,2	MCF-7	breast:
30	chr8:128805941..128809580-chr8:130703915..130707556,3	MCF-7	breast:
31	chr8:130660996..130663314-chr8:130665198..130667685,2	MCF-7	breast:
32	chr8:130707905..130710506-chr8:130721790..130724532,3	K562	blood:
33	chr8:128746735..128749301-chr8:130699107..130701549,4	K562	blood:
34	chr8:130662516..130664208-chr8:130664752..130666833,2	K562	blood:
35	chr8:130685068..130686753-chr8:130736730..130739405,2	K562	blood:
36	chr8:130690016..130691591-chr8:130697534..130699622,2	K562	blood:
37	chr8:128747070..128748818-chr8:130703822..130705821,2	K562	blood:
38	chr8:130662516..130664208-chr8:130664752..130666833,2	K562	blood:
39	chr8:130678074..130680265-chr8:130683828..130686735,2	K562	blood:
40	chr8:130678074..130680265-chr8:130683828..130686735,2	K562	blood:
41	chr8:127888564..127889446-chr8:130699431..130700261,2	K562	blood:
42	chr8:130693991..130694498-chr8:130705234..130705963,2	K562	blood:
43	chr8:130594791..130597296-chr8:130688506..130690853,2	K562	blood:
44	chr8:130692959..130695780-chr8:130701945..130704433,2	K562	blood:
45	chr8:128806162..128808310-chr8:130696628..130698534,2	MCF-7	breast:
46	chr8:128748385..128750737-chr8:130685939..130689386,3	K562	blood:
47	chr8:130694433..130695997-chr8:130696991..130698919,2	K562	blood:
48	chr8:130698168..130701867-chr8:130706682..130711085,4	MCF-7	breast:
49	chr8:130703853..130706502-chr8:130708490..130712451,4	K562	blood:
50	chr8:130694163..130694944-chr8:130737903..130739156,3	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSDMC-1	chr8:130692174-130692485	ENSG00000229140
2	lnc-MYC-3	chr8:130700133-130700624	NONHSAT129111
3	lnc-GSDMC-1	chr8:130692174-130692485	XLOC_007221
4	lnc-GSDMC-1	chr8:130691381-130691566	ENSG00000254223
5	lnc-GSDMC-1	chr8:130692174-130692295	ENSG00000254223
6	lnc-GSDMC-1	chr8:130695818-130695925	ENSG00000254223
7	lnc-GSDMC-4	chr8:130705564-130705921	NONHSAT129128
8	lnc-GSDMC-1	chr8:130694093-130694359	ENSG00000254223

No data

Variant related genes	Relation type
CCDC26	TF binding region
ENSG00000254223	TF binding region
CCDC26	CpG island
ENSG00000254223	CpG island
ENSG00000254223	chromatin interactions
ENSG00000249859	chromatin interactions
ENSG00000224110	chromatin interactions
ENSG00000249375	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000229140	chromatin interactions

Extended variants
information (count: 1966 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:1966 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4626563	chr8:130656205-130656206	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142158134	chr8:130656216-130656217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192151794	chr8:130656272-130656273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35577995	chr8:130656284-130656285	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs532351043	chr8:130656333-130656334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34865413	chr8:130656341-130656342	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs151202853	chr8:130656354-130656355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373879985	chr8:130656358-130656359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561837509	chr8:130656429-130656430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529919275	chr8:130656438-130656439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183132099	chr8:130656472-130656473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566378702	chr8:130656495-130656496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533534843	chr8:130656499-130656500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529106865	chr8:130656508-130656509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113700317	chr8:130656521-130656522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140193252	chr8:130656550-130656551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376236718	chr8:130656592-130656593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375543387	chr8:130656631-130656632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556443302	chr8:130656648-130656649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370637061	chr8:130656659-130656660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187856901	chr8:130656671-130656672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532940348	chr8:130656680-130656681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535809984	chr8:130656687-130656688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149915488	chr8:130656703-130656704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374573043	chr8:130656761-130656762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546173970	chr8:130656793-130656794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564582371	chr8:130656804-130656805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146410963	chr8:130656805-130656806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191217057	chr8:130656809-130656810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551047045	chr8:130656812-130656813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544417939	chr8:130656822-130656823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140804780	chr8:130656825-130656826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368748209	chr8:130656886-130656887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541797457	chr8:130656948-130656949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116842133	chr8:130656979-130656980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201572573	chr8:130656997-130656998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527292446	chr8:130657004-130657005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551712902	chr8:130657073-130657074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376793905	chr8:130657097-130657098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537316917	chr8:130657148-130657149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543173683	chr8:130657172-130657173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549834486	chr8:130657220-130657221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568605279	chr8:130657258-130657259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7830537	chr8:130657263-130657264	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs77033395	chr8:130657289-130657290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566337997	chr8:130657434-130657435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184511131	chr8:130657450-130657451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555665967	chr8:130657548-130657549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558156111	chr8:130657557-130657558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576484168	chr8:130657640-130657641	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:154)

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
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130654400-130656400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:130654800-130656400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:130655200-130656800	Enhancers	Fetal Muscle Leg	muscle
4	chr8:130656000-130657800	Enhancers	Fetal Lung	lung
5	chr8:130656200-130656800	Enhancers	Primary hematopoietic stem cells	blood
6	chr8:130656200-130657200	Enhancers	Osteobl	bone
7	chr8:130656600-130657000	Enhancers	HSMMtube	muscle
8	chr8:130656600-130657400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:130656600-130657400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:130661000-130661600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:130661000-130661600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:130661600-130662000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:130661800-130663000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:130662000-130662200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:130662200-130663400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:130662200-130667200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:130663400-130664400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:130663800-130664400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
19	chr8:130664400-130665600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:130664400-130667600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr8:130665600-130665800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:130665800-130666200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:130666200-130668600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr8:130666800-130668600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr8:130667000-130668000	Enhancers	Dnd41	blood
26	chr8:130667000-130668600	Enhancers	Primary hematopoietic stem cells	blood
27	chr8:130667200-130668600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr8:130667600-130667800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr8:130667600-130668000	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr8:130667600-130668200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr8:130667800-130668200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr8:130668600-130669200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr8:130668800-130670200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
34	chr8:130669200-130671400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr8:130671000-130672200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:130671400-130671600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr8:130671400-130671600	Enhancers	Dnd41	blood
38	chr8:130671400-130672000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:130671600-130673200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:130671600-130673200	Weak transcription	Dnd41	blood
41	chr8:130671600-130673400	Weak transcription	K562	blood
42	chr8:130672000-130674000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr8:130672600-130672800	Enhancers	Primary hematopoietic stem cells	blood
44	chr8:130672800-130675800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr8:130673000-130673200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr8:130673200-130673800	ZNF genes & repeats	Dnd41	blood
47	chr8:130673200-130674000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr8:130673200-130675000	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr8:130673400-130674000	Enhancers	K562	blood
50	chr8:130673800-130674000	Enhancers	Dnd41	blood

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