Variant report

Variant	nsv1031972
Chromosome Location	chr8:11696393-11805961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4671)
CpG islands
(count:3174)
Chromatin interactive
region (count:120)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4671 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11722303-11722739	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11769447-11769628	K562	blood:	n/a	n/a
3	ARID3A	chr8:11746984-11747236	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:11710564-11710991	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:11758928-11760170	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:11719967-11720499	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:11720016-11720613	K562	blood:	n/a	n/a
8	ARID3A	chr8:11754879-11755097	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:11741338-11742065	K562	blood:	n/a	n/a
10	ARID3A	chr8:11801213-11801488	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:11767366-11767469	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:11736830-11737436	K562	blood:	n/a	n/a
13	ARID3A	chr8:11799803-11800003	K562	blood:	n/a	n/a
14	ARID3A	chr8:11743681-11743940	HepG2	liver:	n/a	n/a
15	ARID3A	chr8:11711460-11711976	HepG2	liver:	n/a	n/a
16	ATF1	chr8:11736841-11737531	K562	blood:	n/a	n/a
17	ATF1	chr8:11793688-11793744	K562	blood:	n/a	n/a
18	ATF1	chr8:11799573-11800081	K562	blood:	n/a	n/a
19	ATF1	chr8:11719934-11720561	K562	blood:	n/a	n/a
20	ATF2	chr8:11754354-11755726	GM12878	blood:	n/a	n/a
21	ATF2	chr8:11754279-11755628	GM12878	blood:	n/a	n/a
22	ATF2	chr8:11739306-11739735	GM12878	blood:	n/a	n/a
23	ATF2	chr8:11735207-11736519	GM12878	blood:	n/a	n/a
24	ATF2	chr8:11724597-11725205	GM12878	blood:	n/a	n/a
25	ATF2	chr8:11724806-11725122	GM12878	blood:	n/a	n/a
26	ATF2	chr8:11718234-11718663	GM12878	blood:	n/a	n/a
27	ATF2	chr8:11716064-11716683	GM12878	blood:	n/a	n/a
28	ATF2	chr8:11704572-11705318	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr8:11718117-11718791	GM12878	blood:	n/a	n/a
30	ATF2	chr8:11759720-11760180	GM12878	blood:	n/a	n/a
31	ATF2	chr8:11739202-11739721	GM12878	blood:	n/a	n/a
32	ATF3	chr8:11759787-11760027	K562	blood:	n/a	n/a
33	ATF3	chr8:11720050-11720523	K562	blood:	n/a	n/a
34	ATF3	chr8:11711190-11711884	A549	lung:	n/a	chr8:11711746-11711755
35	ATF3	chr8:11801205-11801436	K562	blood:	n/a	n/a
36	ATF3	chr8:11725482-11725723	HepG2	liver:	n/a	n/a
37	ATF3	chr8:11711440-11711869	K562	blood:	n/a	chr8:11711746-11711755
38	ATF3	chr8:11711524-11711774	K562	blood:	n/a	chr8:11711746-11711755
39	ATF3	chr8:11725467-11725700	K562	blood:	n/a	n/a
40	ATF3	chr8:11801205-11801445	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr8:11720086-11720270	K562	blood:	n/a	n/a
42	BACH1	chr8:11743792-11743922	K562	blood:	n/a	n/a
43	BACH1	chr8:11759765-11760312	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr8:11741878-11742461	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr8:11791553-11791787	K562	blood:	n/a	n/a
46	BACH1	chr8:11766653-11766839	K562	blood:	n/a	n/a
47	BACH1	chr8:11741689-11742495	K562	blood:	n/a	n/a
48	BACH1	chr8:11729699-11729701	H1-hESC	embryonic stem cell:	n/a	n/a
49	BATF	chr8:11764476-11764781	GM12878	blood:	n/a	n/a
50	BATF	chr8:11754746-11755153	GM12878	blood:	n/a	n/a

(count:3174 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11794950-11795000	H1-hESC	embryonic stem cell:	embryo
2	chr8:11795262-11795312	HCF	heart:	n/a
3	chr8:11794950-11795000	H1-hESC	embryonic stem cell:	embryo
4	chr8:11795262-11795312	HCF	heart:	n/a
5	chr8:11726043-11726093	AG04450	lung:	fetal
6	chr8:11795273-11795323	GM19239	blood:	n/a
7	chr8:11771345-11771395	LNCaP	prostate:	n/a
8	chr8:11723816-11723866	HCM	heart:	n/a
9	chr8:11774336-11774386	NH-A	brain:	n/a
10	chr8:11719367-11719417	RPTEC	kidney:	n/a
11	chr8:11717853-11717903	RPTEC	kidney:	n/a
12	chr8:11772734-11772784	SKMC	muscle:	n/a
13	chr8:11790639-11790689	PFSK-1	brain:	n/a
14	chr8:11771244-11771294	AoSMC	blood vessel:	n/a
15	chr8:11726043-11726093	SK-N-MC	brain:	n/a
16	chr8:11760136-11760186	GM06990	blood:	n/a
17	chr8:11759663-11759713	U87	brain:	n/a
18	chr8:11795262-11795312	SK-N-MC	brain:	n/a
19	chr8:11774497-11774547	Hela-S3	cervix:	n/a
20	chr8:11760136-11760186	SK-N-SH_RA	brain:	n/a
21	chr8:11726094-11726144	GM12892	blood:	n/a
22	chr8:11725599-11725649	AG09319	gingival:	n/a
23	chr8:11735419-11735469	MCF-7	breast:	n/a
24	chr8:11771244-11771294	A549	lung:	n/a
25	chr8:11726286-11726336	T-47D	breast:	n/a
26	chr8:11772568-11772618	Caco-2	colon:	n/a
27	chr8:11774336-11774386	HCF	heart:	n/a
28	chr8:11723816-11723866	HUVEC	blood vessel:	n/a
29	chr8:11721826-11721876	HepG2	liver:	n/a
30	chr8:11771345-11771395	HAEpiC	amniotic membrane:	n/a
31	chr8:11726094-11726144	NB4	blood:	n/a
32	chr8:11790559-11790609	SK-N-SH_RA	brain:	n/a
33	chr8:11719367-11719417	HRCEpiC	kidney:	n/a
34	chr8:11771345-11771395	H1-hESC	embryonic stem cell:	embryo
35	chr8:11770970-11771020	HRE	kidney:	n/a
36	chr8:11715284-11715334	NT2-D1	testis:	n/a
37	chr8:11742488-11742538	HAEpiC	amniotic membrane:	n/a
38	chr8:11772119-11772169	HepG2	liver:	n/a
39	chr8:11795273-11795323	BE2_C	brain:	n/a
40	chr8:11772119-11772169	MCF-7	breast:	n/a
41	chr8:11756069-11756119	NT2-D1	testis:	n/a
42	chr8:11770970-11771020	K562	blood:	n/a
43	chr8:11726094-11726144	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:11726286-11726336	RPTEC	kidney:	n/a
45	chr8:11725943-11725993	HepG2	liver:	n/a
46	chr8:11724777-11724827	HRPEpiC	eye:	n/a
47	chr8:11760136-11760186	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:11770970-11771020	SK-N-MC	brain:	n/a
49	chr8:11756069-11756119	HCT-116	colon:	n/a
50	chr8:11759930-11759980	ProgFib	skin:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:11724101..11727184-chr8:11750037..11752895,4	K562	blood:
2	chr8:11723128..11726794-chr8:11729764..11731890,4	MCF-7	breast:
3	chr8:11731939..11733861-chr8:11735868..11738030,2	K562	blood:
4	chr8:11728396..11730707-chr8:11735513..11737265,2	K562	blood:
5	chr8:11709901..11713097-chr8:11718255..11721625,5	MCF-7	breast:
6	chr8:11695946..11697771-chr8:11722616..11724742,2	MCF-7	breast:
7	chr8:11725495..11727126-chr8:11727465..11729533,2	MCF-7	breast:
8	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:
9	chr8:11658066..11660009-chr8:11744623..11746128,2	K562	blood:
10	chr8:11711030..11711819-chr8:11759482..11760312,2	MCF-7	breast:
11	chr8:11746436..11748896-chr8:11754900..11757322,2	K562	blood:
12	chr8:11708512..11715317-chr8:11723234..11727095,9	MCF-7	breast:
13	chr8:11711601..11714581-chr8:11730061..11732215,2	K562	blood:
14	chr8:11622902..11623629-chr8:11759456..11760412,3	MCF-7	breast:
15	chr8:11701610..11705224-chr8:11724505..11726759,3	MCF-7	breast:
16	chr8:11717376..11719253-chr8:11741735..11744320,2	K562	blood:
17	chr8:11625866..11628884-chr8:11724599..11727626,3	MCF-7	breast:
18	chr8:11702698..11703665-chr8:11759456..11760160,2	MCF-7	breast:
19	chr8:11727352..11730707-chr8:11734493..11737265,3	K562	blood:
20	chr11:62608950..62609596-chr8:11725047..11725738,2	HCT-116	colon:
21	chr8:11718826..11720544-chr8:11749993..11751511,2	MCF-7	breast:
22	chr8:11759679..11760322-chr8:11800851..11801844,2	K562	blood:
23	chr8:11718467..11721222-chr8:11754378..11756104,3	K562	blood:
24	chr8:11702751..11703651-chr8:11759392..11760311,3	MCF-7	breast:
25	chr8:11665243..11667469-chr8:11710761..11712863,3	MCF-7	breast:
26	chr8:11734290..11736871-chr8:11743194..11744743,2	K562	blood:
27	chr8:11710201..11712259-chr8:11713212..11714755,2	MCF-7	breast:
28	chr8:11720357..11728660-chr8:11741310..11749437,9	K562	blood:
29	chr8:11662199..11664746-chr8:11796348..11798802,2	K562	blood:
30	chr16:87902576..87903306-chr8:11724748..11725674,2	Hela-S3	cervix:
31	chr20:58672783..58673686-chr8:11698085..11698795,2	NB4	blood:
32	chr8:11727352..11730707-chr8:11734493..11737265,3	K562	blood:
33	chr8:11728396..11730707-chr8:11735513..11737265,2	K562	blood:
34	chr8:11708825..11713035-chr8:11718721..11724039,7	MCF-7	breast:
35	chr8:11746436..11748896-chr8:11754900..11757322,2	K562	blood:
36	chr8:11626549..11628051-chr8:11739939..11742141,2	K562	blood:
37	chr8:11695667..11699183-chr8:11720606..11722768,3	K562	blood:
38	chr8:11658805..11661004-chr8:11802756..11805427,2	K562	blood:
39	chr8:11718857..11721432-chr8:11753489..11755957,2	K562	blood:
40	chr8:11729883..11732100-chr8:11739868..11741394,2	K562	blood:
41	chr8:11709901..11713097-chr8:11718255..11721625,5	MCF-7	breast:
42	chr8:11706290..11708186-chr8:11724044..11726922,3	MCF-7	breast:
43	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
44	chr8:11731939..11733861-chr8:11735868..11738030,2	K562	blood:
45	chr8:11710197..11714536-chr8:11724997..11727273,4	K562	blood:
46	chr8:11723911..11726339-chr8:11798413..11801274,2	K562	blood:
47	chr8:11744571..11746987-chr8:11757045..11759456,2	MCF-7	breast:
48	chr8:11659426..11661474-chr8:11724613..11726870,3	MCF-7	breast:
49	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
50	chr8:11701923..11705144-chr8:11709953..11712815,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTSB-1	chr8:11754271-11754379	NONHSAT125100
2	lnc-FDFT1-1	chr8:11701603-11702070	expReg_chr8_457_+
3	lnc-RP11-297N6.4.1-2	chr8:11703663-11703900	ENSG00000269899.1
4	lnc-CTSB-2	chr8:11777409-11778318	NONHSAT125102
5	lnc-CTSB-1	chr8:11753359-11753626	NONHSAT125100

No data

Variant related genes	Relation type
CTSB	TF binding region
OR7E161P	TF binding region
ENSG00000269899	TF binding region
OR7E158P	TF binding region
ENSG00000255144	TF binding region
CTSB	CpG island
OR7E161P	CpG island
ENSG00000269899	CpG island
OR7E158P	CpG island
ENSG00000255144	CpG island
ENSG00000255144	chromatin interactions
ENSG00000154328	chromatin interactions
ENSG00000269899	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000103257	chromatin interactions
ENSG00000255046	chromatin interactions
ENSG00000079459	chromatin interactions
ENSG00000070961	chromatin interactions
ENSG00000164733	chromatin interactions

Extended variants
information (count: 7057 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:7057 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3189016	chr8:11696394-11696395	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73209010	chr8:11696407-11696408	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs181353551	chr8:11696412-11696413	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549787187	chr8:11696413-11696414	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79603120	chr8:11696423-11696424	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532276196	chr8:11696425-11696426	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540703671	chr8:11696426-11696427	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144342392	chr8:11696437-11696438	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10091118	chr8:11696440-11696441	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs536479503	chr8:11696463-11696464	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558506785	chr8:11696476-11696477	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs8944	chr8:11696492-11696493	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs369701956	chr8:11696508-11696509	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537139896	chr8:11696516-11696517	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141358091	chr8:11696533-11696534	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543203972	chr8:11696537-11696538	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150338237	chr8:11696565-11696566	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573118521	chr8:11696607-11696608	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553670569	chr8:11696610-11696611	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575172316	chr8:11696616-11696617	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2446	chr8:11696677-11696678	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs186367888	chr8:11696729-11696730	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565256339	chr8:11696743-11696744	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142129208	chr8:11696755-11696756	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368004455	chr8:11696787-11696788	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527718722	chr8:11696799-11696800	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189861302	chr8:11696803-11696804	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576094594	chr8:11696824-11696825	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543100505	chr8:11696825-11696826	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564561292	chr8:11696827-11696828	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180770990	chr8:11696839-11696840	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138028654	chr8:11696842-11696843	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559249182	chr8:11696845-11696846	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529945027	chr8:11696873-11696874	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551923299	chr8:11696880-11696881	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547771717	chr8:11696885-11696886	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569711409	chr8:11696895-11696896	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201156627	chr8:11696897-11696898	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149123953	chr8:11696923-11696924	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552678666	chr8:11696930-11696931	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368600271	chr8:11696933-11696934	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143172770	chr8:11696935-11696936	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186452609	chr8:11696941-11696942	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553383255	chr8:11696942-11696943	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549929232	chr8:11696957-11696958	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575116112	chr8:11696960-11696961	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535732292	chr8:11696975-11696976	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557532059	chr8:11696987-11696988	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112884456	chr8:11696993-11696994	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551994437	chr8:11696996-11696997	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:3346 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11667000-11711000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr8:11669400-11708000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:11671400-11701400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:11675200-11707000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:11675800-11712600	Strong transcription	Dnd41	blood
6	chr8:11676200-11704800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:11677000-11705200	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:11677200-11704400	Strong transcription	H9 Cell Line	embryonic stem cell
9	chr8:11677600-11702000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr8:11677600-11702000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:11677600-11703200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:11677600-11708200	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr8:11677600-11710600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr8:11677600-11711800	Strong transcription	Fetal Brain Female	brain
15	chr8:11677800-11706600	Strong transcription	NHLF	lung
16	chr8:11678000-11707400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr8:11678200-11697800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr8:11678200-11704000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:11678200-11704400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr8:11678200-11704600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:11678200-11705200	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr8:11678200-11705200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr8:11678200-11706800	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr8:11678400-11698000	Strong transcription	Duodenum Mucosa	Duodenum
25	chr8:11678400-11704000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:11678400-11704400	Strong transcription	GM12878-XiMat	blood
27	chr8:11678400-11705600	Strong transcription	Fetal Muscle Trunk	muscle
28	chr8:11678400-11706400	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr8:11678600-11705400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:11678600-11708600	Strong transcription	HUVEC	blood vessel
31	chr8:11678800-11697800	Strong transcription	Lung	lung
32	chr8:11679000-11702200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr8:11679000-11705200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
34	chr8:11679000-11715200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr8:11679200-11698800	Strong transcription	Rectal Mucosa Donor 31	rectum
36	chr8:11679200-11710400	Strong transcription	NHDF-Ad	bronchial
37	chr8:11679200-11710800	Strong transcription	Fetal Stomach	stomach
38	chr8:11679400-11705600	Strong transcription	Fetal Lung	lung
39	chr8:11679600-11704200	Strong transcription	K562	blood
40	chr8:11680400-11706600	Strong transcription	HepG2	liver
41	chr8:11682200-11713000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr8:11682400-11712600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr8:11683000-11713200	Strong transcription	Primary B cells from peripheral blood	blood
44	chr8:11683200-11698800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr8:11683200-11698800	Strong transcription	Muscle Satellite Cultured Cells	--
46	chr8:11683200-11698800	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr8:11683200-11706600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr8:11683200-11710000	Strong transcription	NH-A	brain
49	chr8:11683400-11697400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr8:11683400-11698200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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