Variant report

Variant	nsv1015611
Chromosome Location	chr8:130449321-130502086
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:122)
Chromatin interactive
region (count:70)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:130458766-130459136	K562	blood:	n/a	n/a
2	ARID3A	chr8:130468275-130468902	K562	blood:	n/a	n/a
3	ARID3A	chr8:130489794-130490115	K562	blood:	n/a	n/a
4	ATF1	chr8:130489756-130490146	K562	blood:	n/a	n/a
5	ATF1	chr8:130466779-130466951	K562	blood:	n/a	n/a
6	ATF1	chr8:130468278-130468799	K562	blood:	n/a	n/a
7	ATF1	chr8:130452326-130452592	K562	blood:	n/a	n/a
8	ATF1	chr8:130458833-130459202	K562	blood:	n/a	n/a
9	ATF1	chr8:130460055-130460188	K562	blood:	n/a	n/a
10	ATF3	chr8:130449150-130449463	K562	blood:	n/a	n/a
11	BACH1	chr8:130489927-130490190	K562	blood:	n/a	n/a
12	BACH1	chr8:130491336-130491536	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:130457886-130458107	H1-hESC	embryonic stem cell:	n/a	chr8:130458059-130458073
14	BACH1	chr8:130493613-130493739	K562	blood:	n/a	n/a
15	BATF	chr8:130483122-130483340	GM12878	blood:	n/a	chr8:130483257-130483267 chr8:130483256-130483267
16	BATF	chr8:130483047-130483429	GM12878	blood:	n/a	chr8:130483257-130483267 chr8:130483256-130483267
17	BHLHE40	chr8:130458802-130459062	K562	blood:	n/a	n/a
18	BHLHE40	chr8:130468445-130468720	K562	blood:	n/a	n/a
19	BHLHE40	chr8:130497277-130497416	K562	blood:	n/a	n/a
20	CBX3	chr8:130452293-130452793	K562	blood:	n/a	n/a
21	CBX3	chr8:130449011-130449459	K562	blood:	n/a	n/a
22	CCNT2	chr8:130491974-130492774	K562	blood:	n/a	n/a
23	CCNT2	chr8:130468460-130468766	K562	blood:	n/a	n/a
24	CCNT2	chr8:130458771-130459225	K562	blood:	n/a	n/a
25	CEBPB	chr8:130489656-130490047	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:130452429-130452670	K562	blood:	n/a	chr8:130452617-130452634
27	CEBPB	chr8:130452347-130452658	K562	blood:	n/a	chr8:130452617-130452634
28	CEBPB	chr8:130468399-130468814	K562	blood:	n/a	n/a
29	CEBPB	chr8:130449330-130449530	HepG2	liver:	n/a	chr8:130449427-130449438
30	CEBPB	chr8:130462958-130463208	K562	blood:	n/a	chr8:130463078-130463089 chr8:130463078-130463087
31	CEBPB	chr8:130458780-130459144	K562	blood:	n/a	n/a
32	CEBPB	chr8:130468253-130468877	K562	blood:	n/a	n/a
33	CEBPB	chr8:130492445-130492905	IMR90	lung:	n/a	n/a
34	CEBPB	chr8:130460859-130461051	K562	blood:	n/a	n/a
35	CEBPB	chr8:130462896-130463266	K562	blood:	n/a	chr8:130463078-130463089 chr8:130463078-130463087
36	CEBPB	chr8:130458841-130459121	K562	blood:	n/a	n/a
37	CEBPB	chr8:130489702-130489978	K562	blood:	n/a	n/a
38	CEBPB	chr8:130462868-130463271	MCF-7	breast:	n/a	chr8:130463078-130463089 chr8:130463078-130463087
39	CEBPB	chr8:130460106-130460286	K562	blood:	n/a	n/a
40	CEBPB	chr8:130462923-130463238	HepG2	liver:	n/a	chr8:130463078-130463089 chr8:130463078-130463087
41	CEBPB	chr8:130462948-130463247	IMR90	lung:	n/a	chr8:130463078-130463089 chr8:130463078-130463087
42	CEBPB	chr8:130462869-130463269	K562	blood:	n/a	chr8:130463078-130463089 chr8:130463078-130463087
43	CEBPB	chr8:130484639-130484915	K562	blood:	n/a	n/a
44	CEBPB	chr8:130468361-130468837	K562	blood:	n/a	n/a
45	CEBPB	chr8:130449314-130449526	K562	blood:	n/a	chr8:130449427-130449438
46	CTCF	chr8:130458873-130459142	K562	blood:	n/a	n/a
47	CTCF	chr8:130469065-130469121	Fibrobl	skin:	n/a	n/a
48	CTCF	chr8:130501620-130501770	GM06990	blood:	n/a	n/a
49	CTCF	chr8:130458920-130459070	HCM	heart:	n/a	n/a
50	CTCF	chr8:130458940-130459090	HPAF	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:130472165-130472215	HEEpiC	esophagus:	n/a
2	chr8:130472165-130472215	AG09319	gingival:	n/a
3	chr8:130472165-130472215	ECC-1	luminal epithelium:	n/a
4	chr8:130472165-130472215	T-47D	breast:	n/a
5	chr8:130472165-130472215	BJ	skin:	n/a
6	chr8:130492175-130492225	HNPCEpiC	eye:	n/a
7	chr8:130472165-130472215	HNPCEpiC	eye:	n/a
8	chr8:130492175-130492225	PrEC	prostate:	n/a
9	chr8:130492175-130492225	BJ	skin:	n/a
10	chr8:130472165-130472215	Hela-S3	cervix:	n/a
11	chr8:130472165-130472215	ovcar-3	ovarian:	n/a
12	chr8:130492175-130492225	GM12891	blood:	n/a
13	chr8:130472165-130472215	Hepatocyte	liver:	n/a
14	chr8:130472165-130472215	SK-N-SH	brain:	n/a
15	chr8:130472165-130472215	U87	brain:	n/a
16	chr8:130492175-130492225	AG04449	skin:	fetal
17	chr8:130472165-130472215	CMK	blood:	n/a
18	chr8:130472165-130472215	PANC-1	pancreas:	n/a
19	chr8:130472165-130472215	NHBE	bronchial:	n/a
20	chr8:130472165-130472215	SAEC	small airway:	n/a
21	chr8:130492175-130492225	MCF-7	breast:	n/a
22	chr8:130492175-130492225	HEK293	kidney:	embryo
23	chr8:130472165-130472215	NHDF-neo	bronchial:	n/a
24	chr8:130492175-130492225	AG09309	skin:	n/a
25	chr8:130472165-130472215	SK-N-SH_RA	brain:	n/a
26	chr8:130492175-130492225	CMK	blood:	n/a
27	chr8:130492175-130492225	SK-N-SH	brain:	n/a
28	chr8:130492175-130492225	NT2-D1	testis:	n/a
29	chr8:130492175-130492225	HL-60	blood:	n/a
30	chr8:130492175-130492225	HRPEpiC	eye:	n/a
31	chr8:130492175-130492225	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:130472165-130472215	HCPEpiC	choroid plexus:	n/a
33	chr8:130472165-130472215	AoSMC	blood vessel:	n/a
34	chr8:130472165-130472215	HepG2	liver:	n/a
35	chr8:130492175-130492225	HRE	kidney:	n/a
36	chr8:130492175-130492225	MCF10A-Er-Src	breast:	n/a
37	chr8:130492175-130492225	RPTEC	kidney:	n/a
38	chr8:130472165-130472215	HRPEpiC	eye:	n/a
39	chr8:130492175-130492225	LNCaP	prostate:	n/a
40	chr8:130492175-130492225	BE2_C	brain:	n/a
41	chr8:130492175-130492225	A549	lung:	n/a
42	chr8:130472165-130472215	AG04450	lung:	fetal
43	chr8:130492175-130492225	HCF	heart:	n/a
44	chr8:130472165-130472215	HL-60	blood:	n/a
45	chr8:130472165-130472215	NT2-D1	testis:	n/a
46	chr8:130472165-130472215	RPTEC	kidney:	n/a
47	chr8:130492175-130492225	HepG2	liver:	n/a
48	chr8:130472165-130472215	HEK293	kidney:	embryo
49	chr8:130492175-130492225	IMR90	lung:	fetal
50	chr8:130492175-130492225	HRCEpiC	kidney:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:130450871..130455095-chr8:130457353..130461574,6	MCF-7	breast:
2	chr8:130463686..130466426-chr8:130468522..130470101,2	K562	blood:
3	chr8:130473054..130475736-chr8:130477824..130480039,2	K562	blood:
4	chr8:130492675..130494347-chr8:130542077..130543976,2	K562	blood:
5	chr8:130472152..130474277-chr8:130474524..130477153,2	MCF-7	breast:
6	chr8:130477296..130479035-chr8:130481877..130483392,2	K562	blood:
7	chr8:130466558..130470190-chr8:130470932..130474396,4	K562	blood:
8	chr8:130481659..130484565-chr8:130492634..130494986,2	MCF-7	breast:
9	chr8:130461276..130464437-chr8:130465643..130469234,4	MCF-7	breast:
10	chr8:130499002..130501124-chr8:130501495..130503006,2	MCF-7	breast:
11	chr8:130448396..130450929-chr8:130509710..130511491,2	K562	blood:
12	chr8:130454492..130456593-chr8:130464974..130467695,2	K562	blood:
13	chr8:130460320..130462143-chr8:130462300..130463901,2	K562	blood:
14	chr8:130468131..130470642-chr8:130472896..130474611,2	K562	blood:
15	chr8:130446219..130448683-chr8:130450460..130453212,3	K562	blood:
16	chr8:130471335..130473614-chr8:130473626..130476000,2	K562	blood:
17	chr8:130486576..130489479-chr8:130489655..130491776,3	K562	blood:
18	chr8:130468131..130470642-chr8:130472896..130474611,2	K562	blood:
19	chr8:130456549..130458693-chr8:130464674..130467504,3	MCF-7	breast:
20	chr8:130451770..130455234-chr8:130460801..130462723,3	K562	blood:
21	chr8:130466558..130470190-chr8:130470932..130474396,4	K562	blood:
22	chr8:130451014..130452708-chr8:130456649..130459238,2	K562	blood:
23	chr2:46843956..46844785-chr8:130475357..130476300,2	NB4	blood:
24	chr8:130448325..130451235-chr8:130463069..130467328,3	K562	blood:
25	chr8:130450871..130455095-chr8:130457353..130461574,6	MCF-7	breast:
26	chr8:130484819..130486542-chr8:130491250..130493226,2	K562	blood:
27	chr8:130463322..130466804-chr8:130473074..130475467,3	MCF-7	breast:
28	chr8:130472835..130474736-chr8:130481609..130484413,2	K562	blood:
29	chr8:130482902..130485716-chr8:130494024..130496712,3	K562	blood:
30	chr8:130474963..130477166-chr8:130482134..130484641,2	K562	blood:
31	chr8:130443086..130445932-chr8:130472163..130473857,2	MCF-7	breast:
32	chr8:130484819..130486542-chr8:130491250..130493226,2	K562	blood:
33	chr8:130438946..130441544-chr8:130456592..130459697,3	K562	blood:
34	chr8:130472152..130474277-chr8:130474524..130477153,2	MCF-7	breast:
35	chr8:130472835..130474736-chr8:130481609..130484413,2	K562	blood:
36	chr8:130444302..130447418-chr8:130460105..130463114,3	MCF-7	breast:
37	chr8:130451014..130452708-chr8:130456649..130459238,2	K562	blood:
38	chr8:130477296..130479035-chr8:130481877..130483392,2	K562	blood:
39	chr8:130476943..130484127-chr8:130486022..130491772,8	K562	blood:
40	chr8:130473054..130475736-chr8:130477824..130480039,2	K562	blood:
41	chr8:130463686..130466426-chr8:130468522..130470101,2	K562	blood:
42	chr8:130473054..130475813-chr8:130477824..130479965,3	K562	blood:
43	chr8:130460320..130462143-chr8:130462300..130463901,2	K562	blood:
44	chr8:130463322..130466804-chr8:130473074..130475467,3	MCF-7	breast:
45	chr8:130459630..130462121-chr8:130462300..130464633,3	K562	blood:
46	chr8:130451770..130455234-chr8:130460801..130462723,3	K562	blood:
47	chr8:130456549..130458693-chr8:130464674..130467504,3	MCF-7	breast:
48	chr8:130474963..130477166-chr8:130482134..130484641,2	K562	blood:
49	chr8:128748041..128751679-chr8:130463818..130467415,4	MCF-7	breast:
50	chr8:130499002..130501124-chr8:130501495..130503006,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSDMC-1	chr8:130492889-130492936	ENSG00000229140
2	lnc-GSDMC-1	chr8:130492889-130492936	XLOC_007221
3	lnc-MYC-3	chr8:130457499-130458098	NONHSAT129111

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3686	chr8:130496313-130496334	MIMAT0018114

No data

Variant related genes	Relation type
MIR3686	TF binding region
MIR3686	CpG island
ENSG00000229140	chromatin interactions
ENSG00000266387	chromatin interactions
ENSG00000151665	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000263763	chromatin interactions
ENSG00000119878	chromatin interactions

Extended variants
information (count: 1833 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:1833 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6989293	chr8:130449321-130449322	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554539554	chr8:130449388-130449389	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs187001524	chr8:130449395-130449396	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375192222	chr8:130449401-130449402	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs9643250	chr8:130449535-130449536	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs6989725	chr8:130449559-130449560	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs542417374	chr8:130449608-130449609	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs554765204	chr8:130449651-130449652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs6989619	chr8:130449658-130449659	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs540547144	chr8:130449691-130449692	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564522508	chr8:130449713-130449714	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs17262061	chr8:130449774-130449775	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs543900234	chr8:130449800-130449801	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533279547	chr8:130449809-130449810	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529802817	chr8:130449857-130449858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78624759	chr8:130449901-130449902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542756872	chr8:130449944-130449945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560757238	chr8:130449955-130449956	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138426634	chr8:130449973-130449974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552946619	chr8:130449974-130449975	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570858898	chr8:130450013-130450014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs141651592	chr8:130450044-130450045	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192399079	chr8:130450055-130450056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145379374	chr8:130450175-130450176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs137871954	chr8:130450176-130450177	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182435582	chr8:130450196-130450197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs371375013	chr8:130450200-130450201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544842950	chr8:130450272-130450273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573026165	chr8:130450309-130450310	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2217589	chr8:130450346-130450347	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs28545493	chr8:130450353-130450354	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs576726352	chr8:130450389-130450390	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs142401896	chr8:130450394-130450395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562160045	chr8:130450428-130450429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549148193	chr8:130450461-130450462	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs9643251	chr8:130450483-130450484	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs117625378	chr8:130450492-130450493	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs55749850	chr8:130450494-130450495	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs372601399	chr8:130450508-130450509	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs527934797	chr8:130450513-130450514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552807458	chr8:130450564-130450565	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564732158	chr8:130450565-130450566	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148587887	chr8:130450580-130450581	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375239272	chr8:130450635-130450636	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571811780	chr8:130450645-130450646	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs539351181	chr8:130450670-130450671	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141931580	chr8:130450716-130450717	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535560711	chr8:130450717-130450718	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs547908925	chr8:130450738-130450739	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566543956	chr8:130450784-130450785	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:153)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Esophageal adenocarcinoma	18519675	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130446400-130449400	ZNF genes & repeats	Dnd41	blood
2	chr8:130447400-130449400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:130448600-130458800	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr8:130448800-130449400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:130448800-130451000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:130449000-130449400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:130449200-130449400	ZNF genes & repeats	K562	blood
8	chr8:130449200-130449600	Enhancers	NHEK	skin
9	chr8:130449400-130450600	Weak transcription	K562	blood
10	chr8:130449400-130452800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:130450000-130450400	Weak transcription	Dnd41	blood
12	chr8:130450600-130452000	Strong transcription	K562	blood
13	chr8:130451000-130452200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:130451400-130462000	Weak transcription	Thymus	Thymus
15	chr8:130451600-130452600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr8:130451800-130452800	Enhancers	Adipose Nuclei	Adipose
17	chr8:130452000-130454200	Genic enhancers	K562	blood
18	chr8:130452400-130453200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:130452400-130458200	Weak transcription	Fetal Thymus	thymus
20	chr8:130452600-130457800	Weak transcription	Dnd41	blood
21	chr8:130452800-130453800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:130453800-130457400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:130454200-130458000	Strong transcription	K562	blood
24	chr8:130457400-130457800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:130457600-130457800	Enhancers	NHEK	skin
26	chr8:130457800-130458200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr8:130457800-130458400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:130457800-130458800	Genic enhancers	Dnd41	blood
29	chr8:130457800-130458800	Flanking Active TSS	NHEK	skin
30	chr8:130458000-130458200	Enhancers	H9 Cell Line	embryonic stem cell
31	chr8:130458000-130458800	Genic enhancers	K562	blood
32	chr8:130458200-130458600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:130458200-130459200	Enhancers	Fetal Thymus	thymus
34	chr8:130458400-130458600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:130458400-130458800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr8:130458600-130458800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:130458600-130459400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr8:130458600-130459400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:130458600-130459400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:130458800-130459000	Enhancers	H9 Cell Line	embryonic stem cell
41	chr8:130458800-130459000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:130458800-130459200	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr8:130458800-130459200	Enhancers	NHEK	skin
44	chr8:130458800-130459400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr8:130458800-130459400	Transcr. at gene 5' and 3'	K562	blood
46	chr8:130458800-130459600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:130458800-130461600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr8:130458800-130463400	Enhancers	Dnd41	blood
49	chr8:130459000-130459400	Enhancers	Primary B cells from peripheral blood	blood
50	chr8:130459000-130459400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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