Variant report

Variant	nsv893427
Chromosome Location	chr9:71762766-71858517
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2736)
CpG islands
(count:978)
Chromatin interactive
region (count:107)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2736 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71800451-71800521	K562	blood:	n/a	n/a
2	ARID3A	chr9:71805069-71805695	HepG2	liver:	n/a	chr9:71805429-71805445 chr9:71805430-71805446
3	ARID3A	chr9:71830850-71831360	K562	blood:	n/a	n/a
4	ARID3A	chr9:71787032-71787270	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:71808074-71808402	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:71785862-71786328	K562	blood:	n/a	n/a
7	ARID3A	chr9:71795418-71795995	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:71795383-71796025	K562	blood:	n/a	n/a
9	ARID3A	chr9:71788981-71788988	K562	blood:	n/a	n/a
10	ARID3A	chr9:71819420-71819690	K562	blood:	n/a	n/a
11	ARID3A	chr9:71793431-71794296	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:71768528-71769284	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:71808137-71808737	K562	blood:	n/a	n/a
14	ARID3A	chr9:71783969-71784100	HepG2	liver:	n/a	n/a
15	ARID3A	chr9:71821041-71821305	K562	blood:	n/a	n/a
16	ARID3A	chr9:71803674-71804222	K562	blood:	n/a	n/a
17	ARID3A	chr9:71785228-71785657	K562	blood:	n/a	n/a
18	ARID3A	chr9:71801237-71801527	K562	blood:	n/a	n/a
19	ARID3A	chr9:71801110-71801635	HepG2	liver:	n/a	n/a
20	ARID3A	chr9:71802085-71802622	K562	blood:	n/a	n/a
21	ARID3A	chr9:71822394-71822631	K562	blood:	n/a	n/a
22	ARID3A	chr9:71820008-71820023	K562	blood:	n/a	n/a
23	ATF1	chr9:71830870-71831226	K562	blood:	n/a	n/a
24	ATF1	chr9:71785927-71786382	K562	blood:	n/a	n/a
25	ATF1	chr9:71795567-71795986	K562	blood:	n/a	n/a
26	ATF1	chr9:71803941-71804270	K562	blood:	n/a	n/a
27	ATF1	chr9:71802159-71802633	K562	blood:	n/a	n/a
28	ATF2	chr9:71783919-71784211	GM12878	blood:	n/a	n/a
29	ATF2	chr9:71783777-71784242	GM12878	blood:	n/a	n/a
30	ATF2	chr9:71838407-71838832	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr9:71789577-71790776	GM12878	blood:	n/a	n/a
32	ATF2	chr9:71789602-71790821	GM12878	blood:	n/a	n/a
33	ATF3	chr9:71795739-71795903	K562	blood:	n/a	n/a
34	ATF3	chr9:71795571-71796013	K562	blood:	n/a	n/a
35	ATF3	chr9:71830756-71831289	K562	blood:	n/a	n/a
36	BACH1	chr9:71785970-71786100	K562	blood:	n/a	n/a
37	BACH1	chr9:71822637-71822781	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr9:71788674-71789685	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr9:71789894-71790492	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr9:71820997-71821384	H1-hESC	embryonic stem cell:	n/a	n/a
41	BATF	chr9:71783851-71784225	GM12878	blood:	n/a	n/a
42	BATF	chr9:71795660-71795987	GM12878	blood:	n/a	chr9:71795830-71795840 chr9:71795833-71795844
43	BATF	chr9:71783680-71784242	GM12878	blood:	n/a	n/a
44	BATF	chr9:71789947-71790415	GM12878	blood:	n/a	chr9:71790190-71790201
45	BATF	chr9:71791619-71791989	GM12878	blood:	n/a	chr9:71791926-71791934
46	BATF	chr9:71793261-71793492	GM12878	blood:	n/a	n/a
47	BATF	chr9:71789968-71790373	GM12878	blood:	n/a	chr9:71790190-71790201
48	BATF	chr9:71793175-71793610	GM12878	blood:	n/a	n/a
49	BCL11A	chr9:71789879-71790439	GM12878	blood:	n/a	chr9:71790245-71790254
50	BCL11A	chr9:71789969-71790373	GM12878	blood:	n/a	chr9:71790245-71790254

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71787778-71787828	HEK293	kidney:	embryo
2	chr9:71837449-71837499	ECC-1	luminal epithelium:	n/a
3	chr9:71787778-71787828	HEK293	kidney:	embryo
4	chr9:71837449-71837499	ECC-1	luminal epithelium:	n/a
5	chr9:71795999-71796049	Caco-2	colon:	n/a
6	chr9:71795999-71796049	HRCEpiC	kidney:	n/a
7	chr9:71837449-71837499	SK-N-SH	brain:	n/a
8	chr9:71834813-71834863	NHDF-neo	bronchial:	n/a
9	chr9:71836408-71836458	GM12892	blood:	n/a
10	chr9:71792936-71792986	CMK	blood:	n/a
11	chr9:71788759-71788809	HMEC	breast:	n/a
12	chr9:71802071-71802121	NHDF-neo	bronchial:	n/a
13	chr9:71834813-71834863	AoSMC	blood vessel:	n/a
14	chr9:71789653-71789703	CMK	blood:	n/a
15	chr9:71787778-71787828	HCT-116	colon:	n/a
16	chr9:71819910-71819960	SAEC	small airway:	n/a
17	chr9:71789541-71789591	HNPCEpiC	eye:	n/a
18	chr9:71787778-71787828	RPTEC	kidney:	n/a
19	chr9:71819910-71819960	HEK293	kidney:	embryo
20	chr9:71785587-71785637	HL-60	blood:	n/a
21	chr9:71787000-71787050	HRPEpiC	eye:	n/a
22	chr9:71837449-71837499	HIPEpiC	eye:	n/a
23	chr9:71795999-71796049	HCM	heart:	n/a
24	chr9:71788759-71788809	ovcar-3	ovarian:	n/a
25	chr9:71833386-71833436	ProgFib	skin:	n/a
26	chr9:71819910-71819960	IMR90	lung:	fetal
27	chr9:71788759-71788809	AG04449	skin:	fetal
28	chr9:71787778-71787828	HMEC	breast:	n/a
29	chr9:71836408-71836458	HRCEpiC	kidney:	n/a
30	chr9:71788759-71788809	HAEpiC	amniotic membrane:	n/a
31	chr9:71788748-71788798	AG09319	gingival:	n/a
32	chr9:71795999-71796049	AG09309	skin:	n/a
33	chr9:71787160-71787210	Jurkat	blood:	n/a
34	chr9:71785587-71785637	AG04449	skin:	fetal
35	chr9:71833386-71833436	SKMC	muscle:	n/a
36	chr9:71833386-71833436	SK-N-SH_RA	brain:	n/a
37	chr9:71788748-71788798	PFSK-1	brain:	n/a
38	chr9:71788759-71788809	GM12892	blood:	n/a
39	chr9:71785587-71785637	HCF	heart:	n/a
40	chr9:71787000-71787050	HMEC	breast:	n/a
41	chr9:71834813-71834863	AG09309	skin:	n/a
42	chr9:71833386-71833436	ECC-1	luminal epithelium:	n/a
43	chr9:71837449-71837499	HepG2	liver:	n/a
44	chr9:71788759-71788809	NT2-D1	testis:	n/a
45	chr9:71792936-71792986	SK-N-MC	brain:	n/a
46	chr9:71789541-71789591	NHBE	bronchial:	n/a
47	chr9:71802071-71802121	ECC-1	luminal epithelium:	n/a
48	chr9:71789541-71789591	GM06990	blood:	n/a
49	chr9:71787000-71787050	IMR90	lung:	fetal
50	chr9:71789653-71789703	PANC-1	pancreas:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:71734142..71739001-chr9:71788032..71795507,11	MCF-7	breast:
2	chr9:71768614..71770999-chr9:71773509..71775018,2	K562	blood:
3	chr9:71743905..71746446-chr9:71805495..71808231,2	MCF-7	breast:
4	chr9:71789625..71792443-chr9:71836331..71838562,2	K562	blood:
5	chr9:71793542..71796888-chr9:71798932..71802737,4	MCF-7	breast:
6	chr9:71761121..71762822-chr9:71762920..71764542,2	K562	blood:
7	chr9:71819937..71822514-chr9:71828778..71830842,2	K562	blood:
8	chr9:71854349..71857071-chr9:71859863..71862039,2	MCF-7	breast:
9	chr9:71668853..71671288-chr9:71790657..71793201,2	MCF-7	breast:
10	chr9:71821136..71823802-chr9:71938490..71940529,2	MCF-7	breast:
11	chr20:57226307..57226808-chr9:71810144..71810644,2	NB4	blood:
12	chr9:71772812..71775261-chr9:71795422..71797120,2	MCF-7	breast:
13	chr9:71760807..71763605-chr9:71766802..71769126,2	K562	blood:
14	chr9:71798131..71799806-chr9:71811511..71814165,2	MCF-7	breast:
15	chr9:71668686..71669450-chr9:71838137..71838734,2	MCF-7	breast:
16	chr9:71778680..71780994-chr9:71818253..71820499,2	K562	blood:
17	chr9:71812890..71815440-chr9:71822433..71824150,2	MCF-7	breast:
18	chr9:71789625..71792443-chr9:71836331..71838562,2	K562	blood:
19	chr9:71806704..71808402-chr9:71829211..71831372,2	K562	blood:
20	chr9:71794571..71798394-chr9:71798897..71802534,4	K562	blood:
21	chr9:71812890..71815440-chr9:71822433..71824150,2	MCF-7	breast:
22	chr9:71735183..71737374-chr9:71783911..71785475,2	MCF-7	breast:
23	chr9:71780838..71784047-chr9:71785849..71788919,3	MCF-7	breast:
24	chr9:71782411..71787293-chr9:71788939..71792215,6	K562	blood:
25	chr9:71774601..71776858-chr9:71777097..71779223,2	K562	blood:
26	chr9:71850777..71853807-chr9:71854436..71856252,3	K562	blood:
27	chr9:71650597..71652252-chr9:71824888..71827818,2	MCF-7	breast:
28	chr9:71794571..71798394-chr9:71798897..71802534,4	K562	blood:
29	chr9:71830973..71832633-chr9:71834177..71836449,2	K562	blood:
30	chr9:71743521..71745547-chr9:71821447..71823888,2	MCF-7	breast:
31	chr9:71745094..71746594-chr9:71762879..71765148,2	MCF-7	breast:
32	chr9:71768851..71770406-chr9:71807672..71810117,2	MCF-7	breast:
33	chr9:71785836..71791669-chr9:71792328..71797551,11	K562	blood:
34	chr9:71782838..71785289-chr9:71817558..71819101,2	MCF-7	breast:
35	chr9:71793727..71795446-chr9:71807376..71809123,2	MCF-7	breast:
36	chr9:71760807..71763605-chr9:71766802..71769126,2	K562	blood:
37	chr9:71735620..71737619-chr9:71808217..71809770,2	MCF-7	breast:
38	chr9:71774886..71777196-chr9:71788478..71790198,2	MCF-7	breast:
39	chr9:71830235..71832170-chr9:71836510..71838640,2	K562	blood:
40	chr9:71784445..71787673-chr9:71788744..71791713,5	K562	blood:
41	chr9:71813787..71816021-chr9:71816458..71819040,2	K562	blood:
42	chr9:71768614..71770999-chr9:71773509..71775018,2	K562	blood:
43	chr9:71798131..71799806-chr9:71811511..71814165,2	MCF-7	breast:
44	chr9:71736310..71738206-chr9:71797242..71798901,2	MCF-7	breast:
45	chr9:71850777..71853807-chr9:71854436..71856252,3	K562	blood:
46	chr9:71686014..71689293-chr9:71805643..71807349,3	K562	blood:
47	chr9:71788912..71791294-chr9:71803857..71806378,3	MCF-7	breast:
48	chr9:71768851..71770406-chr9:71807672..71810117,2	MCF-7	breast:
49	chr9:71807885..71810232-chr9:71825677..71828863,3	K562	blood:
50	chr9:71730545..71732525-chr9:71797822..71800476,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APBA1-6	chr9:71855143-71855736	NONHSAT131773
2	lnc-PRKACG-2	chr9:71780235-71782388	ENSG00000250944
3	lnc-PRKACG-2	chr9:71785572-71785971	ENSG00000250944

No data

Variant related genes	Relation type
TJP2	TF binding region
TJP2	CpG island
ENSG00000165060	chromatin interactions
ENSG00000254995	chromatin interactions
ENSG00000119139	chromatin interactions
ENSG00000124222	chromatin interactions
ENSG00000135063	chromatin interactions
APITD1	miRNA target sites
FLOT1	miRNA target sites

Extended variants
information (count: 3870 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3870 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10781440	chr9:71762766-71762767	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554273710	chr9:71762789-71762790	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs534489321	chr9:71762814-71762815	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs140620964	chr9:71762842-71762843	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs539940147	chr9:71762856-71762857	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs575942680	chr9:71762891-71762892	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs543370270	chr9:71762897-71762898	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564872377	chr9:71762908-71762909	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs140251704	chr9:71762933-71762934	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs540876927	chr9:71762955-71762956	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs559113281	chr9:71762963-71762964	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs371693514	chr9:71762990-71762991	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs10156651	chr9:71763088-71763089	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs10156634	chr9:71763108-71763109	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs371295541	chr9:71763126-71763127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561148842	chr9:71763148-71763149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531695664	chr9:71763170-71763171	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34986827	chr9:71763191-71763192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550183428	chr9:71763210-71763211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114762151	chr9:71763276-71763277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539336483	chr9:71763286-71763287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs74364759	chr9:71763304-71763305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11145442	chr9:71763362-71763363	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs566234703	chr9:71763412-71763413	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs72538840	chr9:71763451-71763452	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs386414983	chr9:71763452-71763453	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs80205243	chr9:71763453-71763454	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544394230	chr9:71763466-71763467	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540190669	chr9:71763495-71763496	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554618105	chr9:71763528-71763529	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs576043234	chr9:71763537-71763538	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs537080199	chr9:71763538-71763539	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs558129924	chr9:71763580-71763581	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs576769864	chr9:71763581-71763582	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs190571582	chr9:71763597-71763598	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs111274748	chr9:71763604-71763605	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs73449120	chr9:71763687-71763688	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs140856938	chr9:71763690-71763691	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542771354	chr9:71763720-71763721	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150142721	chr9:71763783-71763784	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138611869	chr9:71763820-71763821	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550244866	chr9:71763882-71763883	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565919508	chr9:71763911-71763912	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577462168	chr9:71763933-71763934	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565266853	chr9:71763954-71763955	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34779414	chr9:71763986-71763987	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12005295	chr9:71764026-71764027	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548062536	chr9:71764039-71764040	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566161946	chr9:71764155-71764156	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149296851	chr9:71764160-71764161	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:3651 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71738000-71778200	Weak transcription	Primary T cells from cord blood	blood
2	chr9:71738200-71770600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr9:71745400-71770600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr9:71746200-71764400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr9:71746400-71783200	Weak transcription	Small Intestine	intestine
6	chr9:71747000-71768600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:71747000-71775600	Weak transcription	Hela-S3	cervix
8	chr9:71747200-71764200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr9:71747200-71764200	Weak transcription	Fetal Kidney	kidney
10	chr9:71747200-71766800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr9:71747200-71769800	Weak transcription	Placenta	Placenta
12	chr9:71747600-71764200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:71747600-71764400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr9:71747800-71764200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr9:71748400-71764200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr9:71748400-71764800	Weak transcription	Aorta	Aorta
17	chr9:71749600-71764200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr9:71749800-71764200	Weak transcription	Fetal Stomach	stomach
19	chr9:71749800-71770200	Weak transcription	Esophagus	oesophagus
20	chr9:71749800-71770200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr9:71749800-71780600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:71750000-71764200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr9:71750000-71764200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr9:71752000-71767400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:71752000-71768600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr9:71752000-71780600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr9:71752000-71788600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr9:71753000-71764400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr9:71753200-71764200	Weak transcription	Liver	Liver
30	chr9:71753200-71764400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr9:71753200-71766600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:71753200-71778800	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr9:71753400-71765600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr9:71754600-71766600	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr9:71755400-71763400	Weak transcription	Gastric	stomach
36	chr9:71755600-71763600	Strong transcription	HepG2	liver
37	chr9:71755600-71788600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr9:71757000-71764400	Weak transcription	Fetal Intestine Large	intestine
39	chr9:71757200-71763600	Weak transcription	Right Ventricle	heart
40	chr9:71757200-71764400	Weak transcription	Left Ventricle	heart
41	chr9:71757400-71766800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr9:71757600-71783800	Weak transcription	Stomach Mucosa	stomach
43	chr9:71758400-71764200	Weak transcription	Fetal Lung	lung
44	chr9:71758400-71766600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr9:71758600-71764000	Weak transcription	Brain Substantia Nigra	brain
46	chr9:71758600-71764200	Weak transcription	Brain Anterior Caudate	brain
47	chr9:71758600-71764200	Weak transcription	Brain Hippocampus Middle	brain
48	chr9:71758600-71764200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr9:71758800-71764000	Weak transcription	Brain Cingulate Gyrus	brain
50	chr9:71758800-71764200	Weak transcription	HMEC	breast

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