Variant report

Variant	nsv498082
Chromosome Location	chr8:19722435-19873112
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:845)
CpG islands
(count:1037)
Chromatin interactive
region (count:41)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:19752064-19752243	K562	blood:	n/a	n/a
2	ATF1	chr8:19748706-19748730	K562	blood:	n/a	n/a
3	BACH1	chr8:19843360-19843572	K562	blood:	n/a	n/a
4	BACH1	chr8:19796944-19797834	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:19843304-19843645	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:19785716-19786014	GM12878	blood:	n/a	n/a
7	BATF	chr8:19870526-19870831	GM12878	blood:	n/a	chr8:19870633-19870644
8	BHLHE40	chr8:19797814-19797998	K562	blood:	n/a	n/a
9	BHLHE40	chr8:19796833-19796991	K562	blood:	n/a	n/a
10	BHLHE40	chr8:19794421-19794792	K562	blood:	n/a	n/a
11	BHLHE40	chr8:19727856-19728054	K562	blood:	n/a	n/a
12	BHLHE40	chr8:19727841-19728121	GM12878	blood:	n/a	n/a
13	BRCA1	chr8:19732279-19732313	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr8:19844778-19845080	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr8:19796929-19797620	K562	blood:	n/a	n/a
16	CEBPB	chr8:19795244-19795466	IMR90	lung:	n/a	chr8:19795312-19795323 chr8:19795313-19795324 chr8:19795314-19795323
17	CEBPB	chr8:19813568-19813758	HepG2	liver:	n/a	chr8:19813635-19813646
18	CEBPB	chr8:19794485-19794712	H1-hESC	embryonic stem cell:	n/a	chr8:19794653-19794661
19	CEBPB	chr8:19785496-19785795	Hela-S3	cervix:	n/a	chr8:19785649-19785660
20	CEBPB	chr8:19785486-19785799	K562	blood:	n/a	chr8:19785649-19785660
21	CEBPB	chr8:19749024-19749191	A549	lung:	n/a	n/a
22	CEBPB	chr8:19795162-19795476	K562	blood:	n/a	chr8:19795312-19795323 chr8:19795313-19795324 chr8:19795314-19795323
23	CEBPB	chr8:19795159-19795488	A549	lung:	n/a	chr8:19795312-19795323 chr8:19795313-19795324 chr8:19795314-19795323
24	CEBPB	chr8:19785507-19785778	A549	lung:	n/a	chr8:19785649-19785660
25	CEBPB	chr8:19798725-19799014	Hela-S3	cervix:	n/a	chr8:19798852-19798863
26	CEBPB	chr8:19844693-19845566	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:19785493-19785792	K562	blood:	n/a	chr8:19785649-19785660
28	CEBPB	chr8:19794433-19794744	Hela-S3	cervix:	n/a	chr8:19794653-19794661
29	CEBPB	chr8:19830299-19830813	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr8:19785497-19785800	IMR90	lung:	n/a	chr8:19785649-19785660
31	CEBPB	chr8:19795168-19795499	Hela-S3	cervix:	n/a	chr8:19795312-19795323 chr8:19795313-19795324 chr8:19795314-19795323
32	CEBPB	chr8:19803092-19803381	Hela-S3	cervix:	n/a	chr8:19803234-19803245 chr8:19803232-19803245 chr8:19803232-19803245 chr8:19803313-19803324
33	CEBPB	chr8:19795161-19795482	HepG2	liver:	n/a	chr8:19795312-19795323 chr8:19795313-19795324 chr8:19795314-19795323
34	CEBPB	chr8:19785498-19785796	H1-hESC	embryonic stem cell:	n/a	chr8:19785649-19785660
35	CEBPB	chr8:19785494-19785795	HepG2	liver:	n/a	chr8:19785649-19785660
36	CHD1	chr8:19866270-19866323	GM12878	blood:	n/a	n/a
37	CHD1	chr8:19797168-19797365	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr8:19794434-19794791	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr8:19794483-19794780	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr8:19796456-19797489	H1-hESC	embryonic stem cell:	n/a	chr8:19797440-19797447
41	CHD2	chr8:19797201-19797317	K562	blood:	n/a	n/a
42	CHD2	chr8:19732364-19732392	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTBP2	chr8:19796489-19798092	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:19786460-19786610	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr8:19786480-19786630	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr8:19801539-19801593	GM13976	blood:	n/a	n/a
47	CTCF	chr8:19786440-19786590	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr8:19727880-19728030	HUVEC	blood vessel:	n/a	chr8:19727986-19728004 chr8:19727989-19728002 chr8:19727987-19728003 chr8:19727988-19728009 chr8:19727989-19727997
49	CTCF	chr8:19786436-19786603	K562	blood:	n/a	n/a
50	CTCF	chr8:19727700-19727850	GM12801	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19796591-19796641	SK-N-SH_RA	brain:	n/a
2	chr8:19797134-19797184	AG10803	skin:	n/a
3	chr8:19796335-19796385	PrEC	prostate:	n/a
4	chr8:19794539-19794589	HUVEC	blood vessel:	n/a
5	chr8:19798005-19798055	ECC-1	luminal epithelium:	n/a
6	chr8:19796561-19796611	H1-hESC	embryonic stem cell:	embryo
7	chr8:19797965-19798015	AG10803	skin:	n/a
8	chr8:19797134-19797184	HRPEpiC	eye:	n/a
9	chr8:19796591-19796641	BJ	skin:	n/a
10	chr8:19797445-19797495	SK-N-SH_RA	brain:	n/a
11	chr8:19823147-19823197	ProgFib	skin:	n/a
12	chr8:19794539-19794589	HCF	heart:	n/a
13	chr8:19797965-19798015	Caco-2	colon:	n/a
14	chr8:19794539-19794589	RPTEC	kidney:	n/a
15	chr8:19798765-19798815	RPTEC	kidney:	n/a
16	chr8:19799278-19799328	ovcar-3	ovarian:	n/a
17	chr8:19866173-19866223	SKMC	muscle:	n/a
18	chr8:19800242-19800292	AG10803	skin:	n/a
19	chr8:19797965-19798015	U87	brain:	n/a
20	chr8:19798765-19798815	HCPEpiC	choroid plexus:	n/a
21	chr8:19866173-19866223	ProgFib	skin:	n/a
22	chr8:19796533-19796583	T-47D	breast:	n/a
23	chr8:19798765-19798815	MCF-7	breast:	n/a
24	chr8:19798005-19798055	AG04449	skin:	fetal
25	chr8:19797445-19797495	HMEC	breast:	n/a
26	chr8:19799278-19799328	HCM	heart:	n/a
27	chr8:19796844-19796894	HUVEC	blood vessel:	n/a
28	chr8:19797445-19797495	HCF	heart:	n/a
29	chr8:19866173-19866223	IMR90	lung:	fetal
30	chr8:19800242-19800292	A549	lung:	n/a
31	chr8:19796533-19796583	HIPEpiC	eye:	n/a
32	chr8:19798765-19798815	SK-N-SH	brain:	n/a
33	chr8:19796394-19796444	HNPCEpiC	eye:	n/a
34	chr8:19798005-19798055	GM12892	blood:	n/a
35	chr8:19794539-19794589	Jurkat	blood:	n/a
36	chr8:19823147-19823197	SK-N-SH_RA	brain:	n/a
37	chr8:19796591-19796641	AG09319	gingival:	n/a
38	chr8:19823147-19823197	K562	blood:	n/a
39	chr8:19797445-19797495	HCT-116	colon:	n/a
40	chr8:19796335-19796385	U87	brain:	n/a
41	chr8:19796394-19796444	BJ	skin:	n/a
42	chr8:19796394-19796444	HRE	kidney:	n/a
43	chr8:19798005-19798055	HL-60	blood:	n/a
44	chr8:19794539-19794589	CMK	blood:	n/a
45	chr8:19796533-19796583	PANC-1	pancreas:	n/a
46	chr8:19796299-19796349	HCM	heart:	n/a
47	chr8:19798005-19798055	HRE	kidney:	n/a
48	chr8:19800242-19800292	ovcar-3	ovarian:	n/a
49	chr8:19796561-19796611	AG04449	skin:	fetal
50	chr8:19798765-19798815	A549	lung:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:19786191..19787478-chr8:19970989..19972023,3	K562	blood:
2	chr8:19793876..19796137-chr8:19796466..19799568,3	K562	blood:
3	chr8:19777298..19780143-chr8:19794584..19796996,2	K562	blood:
4	chr8:19845716..19848259-chr8:19851738..19854660,2	K562	blood:
5	chr8:19807869..19810930-chr8:19812485..19816612,3	K562	blood:
6	chr8:19835726..19838194-chr8:19839836..19842333,2	K562	blood:
7	chr8:19869466..19870969-chr8:19928497..19931121,2	K562	blood:
8	chr8:19797563..19799546-chr8:19810189..19812255,2	K562	blood:
9	chr8:19805034..19807326-chr8:19809169..19811109,2	K562	blood:
10	chr8:19727136..19729555-chr8:19732389..19735213,2	K562	blood:
11	chr8:19727939..19728690-chr8:19971015..19972062,3	MCF-7	breast:
12	chr8:19805034..19807326-chr8:19809169..19811109,2	K562	blood:
13	chr8:19811879..19814750-chr8:19820326..19823164,2	K562	blood:
14	chr8:19796997..19799625-chr8:19800573..19802091,2	K562	blood:
15	chr8:19747137..19751203-chr8:19751679..19754086,4	K562	blood:
16	chr8:19726580..19729500-chr8:19735751..19737530,2	K562	blood:
17	chr8:19807869..19810930-chr8:19812485..19816612,3	K562	blood:
18	chr8:19811879..19814750-chr8:19820326..19823164,2	K562	blood:
19	chr8:19727405..19728444-chr8:19980912..19981476,3	MCF-7	breast:
20	chr8:19727572..19728249-chr8:19990904..19991781,3	K562	blood:
21	chr8:19835726..19838194-chr8:19839836..19842333,2	K562	blood:
22	chr8:19800611..19802825-chr8:20055037..20057972,2	MCF-7	breast:
23	chr8:19727136..19729555-chr8:19732389..19735213,2	K562	blood:
24	chr8:19820325..19822189-chr8:19825271..19827083,2	K562	blood:
25	chr8:19786061..19786740-chr8:19980944..19981679,3	K562	blood:
26	chr8:19737734..19739441-chr8:19740524..19742384,2	K562	blood:
27	chr8:19820325..19822189-chr8:19825271..19827083,2	K562	blood:
28	chr8:19786443..19786979-chr8:19980934..19981886,2	MCF-7	breast:
29	chr8:19796366..19798853-chr8:19819344..19821479,2	K562	blood:
30	chr8:19737734..19739441-chr8:19740524..19742384,2	K562	blood:
31	chr8:19726580..19729500-chr8:19735751..19737530,2	K562	blood:
32	chr8:19747137..19751203-chr8:19751679..19754086,4	K562	blood:
33	chr8:19786079..19786796-chr8:20233434..20233934,2	K562	blood:
34	chr8:19796997..19799625-chr8:19800573..19802091,2	K562	blood:
35	chr8:19797563..19799546-chr8:19810189..19812255,2	K562	blood:
36	chr8:19727581..19728428-chr8:19971178..19971906,3	MCF-7	breast:
37	chr8:19847973..19850386-chr8:19927067..19928917,2	K562	blood:
38	chr8:19675302..19676840-chr8:19775032..19777867,2	K562	blood:
39	chr8:19797802..19799354-chr8:19971667..19974269,2	K562	blood:
40	chr8:19845716..19848259-chr8:19851738..19854660,2	K562	blood:
41	chr8:19786007..19786963-chr8:19971036..19972051,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSGALNACT1-2	chr8:19782569-19782680	XLOC_007017
2	lnc-LPL-1	chr8:19750703-19750937	expReg_chr8_827_+
3	lnc-CSGALNACT1-2	chr8:19780259-19780459	XLOC_007017

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LPL	hsa-miR-29a-3p	chr8:19824603-19824624
2	LPL	hsa-miR-29a-3p	chr8:19824617-19824624

Variant related genes	Relation type
LPL	TF binding region
LPL	CpG island
ENSG00000175445	chromatin interactions
ENSG00000242709	chromatin interactions

Extended variants
information (count: 5344 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:5344 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115173572	chr8:19722483-19722484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547132747	chr8:19722507-19722508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs386723267	chr8:19722555-19722556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11998681	chr8:19722560-19722561	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs558588635	chr8:19722571-19722572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571981074	chr8:19722580-19722581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541002768	chr8:19722583-19722584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372982651	chr8:19722585-19722586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377333545	chr8:19722608-19722609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192106320	chr8:19722627-19722628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574380687	chr8:19722632-19722633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79959150	chr8:19722633-19722634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543304455	chr8:19722664-19722665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182848582	chr8:19722686-19722687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531897679	chr8:19722708-19722709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147061436	chr8:19722717-19722718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565354742	chr8:19722726-19722727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76753032	chr8:19722813-19722814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150639794	chr8:19722870-19722871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147882708	chr8:19722874-19722875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151203088	chr8:19722903-19722904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375520307	chr8:19722910-19722911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78382464	chr8:19722922-19722923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191638244	chr8:19722947-19722948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182720957	chr8:19722960-19722961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187410609	chr8:19722963-19722964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558397749	chr8:19722971-19722972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370565996	chr8:19723016-19723017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572106010	chr8:19723043-19723044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62651342	chr8:19723064-19723065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192067257	chr8:19723079-19723080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140281848	chr8:19723093-19723094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543356981	chr8:19723095-19723096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148685495	chr8:19723120-19723121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527631398	chr8:19723164-19723165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373878742	chr8:19723170-19723171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568173690	chr8:19723179-19723180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150684896	chr8:19723226-19723227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536730377	chr8:19723231-19723232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371257878	chr8:19723241-19723242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563156816	chr8:19723256-19723257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550788676	chr8:19723266-19723267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570307627	chr8:19723267-19723268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376846153	chr8:19723273-19723274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373673007	chr8:19723277-19723278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201018837	chr8:19723296-19723297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201874373	chr8:19723297-19723298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71205950	chr8:19723309-19723310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552867759	chr8:19723329-19723330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140799035	chr8:19723333-19723334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	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
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19718600-19732200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:19722200-19722600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:19724800-19725000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:19724800-19725000	Enhancers	Fetal Kidney	kidney
5	chr8:19725200-19731200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:19725600-19725800	Enhancers	Fetal Kidney	kidney
7	chr8:19726400-19732400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:19726800-19730200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:19727200-19728600	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr8:19727200-19728800	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr8:19727200-19729000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:19727200-19729000	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr8:19727800-19728000	Bivalent Enhancer	Primary B cells from cord blood	blood
14	chr8:19728000-19728400	Active TSS	Rectal Mucosa Donor 29	rectum
15	chr8:19728000-19729000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:19728000-19729600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr8:19728000-19732800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr8:19728200-19728400	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr8:19728200-19728600	Enhancers	Fetal Lung	lung
20	chr8:19728200-19728800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:19728200-19728800	Enhancers	Adipose Nuclei	Adipose
22	chr8:19728200-19728800	Enhancers	Stomach Mucosa	stomach
23	chr8:19728200-19729000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:19728200-19729000	Enhancers	Hela-S3	cervix
25	chr8:19728200-19729200	Enhancers	HepG2	liver
26	chr8:19728200-19731200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:19728200-19731800	Enhancers	H9 Cell Line	embryonic stem cell
28	chr8:19728200-19733400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr8:19728200-19734000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:19728400-19728800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:19728400-19728800	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr8:19728400-19728800	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr8:19728400-19728800	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr8:19728400-19729000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:19728400-19729200	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:19728400-19729400	Enhancers	Placenta	Placenta
37	chr8:19728400-19730000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr8:19728400-19733600	Enhancers	Duodenum Mucosa	Duodenum
39	chr8:19728600-19728800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr8:19728600-19728800	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
41	chr8:19728600-19730000	Weak transcription	Fetal Lung	lung
42	chr8:19728600-19733600	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr8:19728800-19729400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr8:19728800-19729600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr8:19728800-19730000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr8:19728800-19730400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr8:19728800-19731200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:19728800-19733200	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr8:19728800-19733200	Weak transcription	Adipose Nuclei	Adipose
50	chr8:19729000-19729400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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