Variant report

Variant	nsv875482
Chromosome Location	chr2:183508696-183582170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1349)
CpG islands
(count:734)
Chromatin interactive
region (count:49)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183514101-183514302	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183515581-183515755	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:183580474-183581183	HepG2	liver:	n/a	n/a
4	ATF2	chr2:183580660-183581148	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:183580338-183581152	GM12878	blood:	n/a	n/a
6	ATF2	chr2:183580660-183581085	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr2:183580790-183581114	K562	blood:	n/a	chr2:183580978-183580987
8	BACH1	chr2:183581406-183581577	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:183581032-183581106	K562	blood:	n/a	n/a
10	BACH1	chr2:183515561-183515598	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:183580525-183581202	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr2:183580410-183581093	A549	lung:	n/a	chr2:183580912-183580925 chr2:183580685-183580694 chr2:183580748-183580761 chr2:183580903-183580916 chr2:183580753-183580766
13	BCLAF1	chr2:183580322-183581201	GM12878	blood:	n/a	chr2:183580912-183580925 chr2:183580685-183580694 chr2:183580748-183580761 chr2:183580903-183580916 chr2:183580753-183580766
14	BHLHE40	chr2:183580447-183581508	GM12878	blood:	n/a	chr2:183580750-183580766 chr2:183580968-183580984 chr2:183580900-183580916 chr2:183580742-183580758 chr2:183580753-183580769 chr2:183580910-183580926
15	BHLHE40	chr2:183580177-183581631	K562	blood:	n/a	chr2:183580750-183580766 chr2:183580968-183580984 chr2:183580900-183580916 chr2:183580742-183580758 chr2:183580753-183580769 chr2:183580910-183580926
16	BHLHE40	chr2:183580015-183581390	HepG2	liver:	n/a	chr2:183580750-183580766 chr2:183580968-183580984 chr2:183580900-183580916 chr2:183580742-183580758 chr2:183580753-183580769 chr2:183580910-183580926
17	BHLHE40	chr2:183511689-183511769	K562	blood:	n/a	n/a
18	BHLHE40	chr2:183581895-183581916	GM12878	blood:	n/a	n/a
19	BRCA1	chr2:183580850-183581133	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr2:183580727-183581109	HepG2	liver:	n/a	n/a
21	BRCA1	chr2:183515566-183515708	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr2:183515397-183515792	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr2:183576504-183576579	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr2:183580321-183581659	K562	blood:	n/a	n/a
25	CCNT2	chr2:183580601-183581535	K562	blood:	n/a	n/a
26	CEBPB	chr2:183515407-183515756	A549	lung:	n/a	n/a
27	CEBPB	chr2:183515398-183515762	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr2:183515356-183515775	K562	blood:	n/a	n/a
29	CEBPB	chr2:183525284-183525460	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:183579912-183580208	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:183570553-183570787	K562	blood:	n/a	chr2:183570625-183570636 chr2:183570624-183570635 chr2:183570624-183570637
32	CEBPB	chr2:183515326-183515830	HCT-116	colon:	n/a	n/a
33	CEBPB	chr2:183515280-183515751	A549	lung:	n/a	n/a
34	CEBPB	chr2:183515260-183515819	HCT-116	colon:	n/a	n/a
35	CEBPB	chr2:183515306-183515761	MCF-7	breast:	n/a	n/a
36	CEBPB	chr2:183530344-183530385	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:183580683-183581080	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:183570581-183570783	HepG2	liver:	n/a	chr2:183570625-183570636 chr2:183570624-183570635 chr2:183570624-183570637
39	CEBPB	chr2:183558932-183559246	A549	lung:	n/a	chr2:183559095-183559106
40	CEBPB	chr2:183515392-183515766	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr2:183533497-183533760	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:183558939-183559230	K562	blood:	n/a	chr2:183559095-183559106
43	CEBPB	chr2:183515467-183515816	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr2:183546942-183547197	K562	blood:	n/a	n/a
45	CEBPB	chr2:183580798-183580804	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:183579897-183580654	A549	lung:	n/a	n/a
47	CEBPB	chr2:183515403-183515763	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:183515383-183515777	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:183558920-183559274	HepG2	liver:	n/a	chr2:183559095-183559106
50	CEBPB	chr2:183515407-183515765	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183580950-183581000	MCF-7	breast:	n/a
2	chr2:183580523-183580573	Hepatocyte	liver:	n/a
3	chr2:183580950-183581000	MCF-7	breast:	n/a
4	chr2:183580523-183580573	Hepatocyte	liver:	n/a
5	chr2:183581591-183581641	AG10803	skin:	n/a
6	chr2:183580694-183580744	HEEpiC	esophagus:	n/a
7	chr2:183580463-183580513	AG09319	gingival:	n/a
8	chr2:183580523-183580573	CMK	blood:	n/a
9	chr2:183580523-183580573	AG09309	skin:	n/a
10	chr2:183580906-183580956	BJ	skin:	n/a
11	chr2:183580574-183580624	GM12892	blood:	n/a
12	chr2:183580841-183580891	GM19239	blood:	n/a
13	chr2:183580523-183580573	NT2-D1	testis:	n/a
14	chr2:183580463-183580513	HUVEC	blood vessel:	n/a
15	chr2:183580818-183580868	SK-N-SH_RA	brain:	n/a
16	chr2:183580906-183580956	ProgFib	skin:	n/a
17	chr2:183580910-183580960	GM12878	blood:	n/a
18	chr2:183580829-183580879	ECC-1	luminal epithelium:	n/a
19	chr2:183577625-183577675	SK-N-SH_RA	brain:	n/a
20	chr2:183580574-183580624	HRPEpiC	eye:	n/a
21	chr2:183580841-183580891	HRCEpiC	kidney:	n/a
22	chr2:183580906-183580956	BE2_C	brain:	n/a
23	chr2:183580818-183580868	AG09309	skin:	n/a
24	chr2:183580841-183580891	NT2-D1	testis:	n/a
25	chr2:183580523-183580573	NHBE	bronchial:	n/a
26	chr2:183580910-183580960	K562	blood:	n/a
27	chr2:183580574-183580624	Hepatocyte	liver:	n/a
28	chr2:183581591-183581641	HCPEpiC	choroid plexus:	n/a
29	chr2:183580818-183580868	BJ	skin:	n/a
30	chr2:183580910-183580960	PrEC	prostate:	n/a
31	chr2:183580950-183581000	HNPCEpiC	eye:	n/a
32	chr2:183580818-183580868	PFSK-1	brain:	n/a
33	chr2:183581591-183581641	A549	lung:	n/a
34	chr2:183580818-183580868	H1-hESC	embryonic stem cell:	embryo
35	chr2:183580950-183581000	AoSMC	blood vessel:	n/a
36	chr2:183580523-183580573	Hela-S3	cervix:	n/a
37	chr2:183580574-183580624	NB4	blood:	n/a
38	chr2:183580906-183580956	AG04449	skin:	fetal
39	chr2:183581591-183581641	IMR90	lung:	fetal
40	chr2:183580694-183580744	NHDF-neo	bronchial:	n/a
41	chr2:183580463-183580513	SK-N-MC	brain:	n/a
42	chr2:183580950-183581000	HCM	heart:	n/a
43	chr2:183580463-183580513	GM12892	blood:	n/a
44	chr2:183580574-183580624	RPTEC	kidney:	n/a
45	chr2:183580523-183580573	HEK293	kidney:	embryo
46	chr2:183580841-183580891	GM06990	blood:	n/a
47	chr2:183580818-183580868	GM12878	blood:	n/a
48	chr2:183580574-183580624	ovcar-3	ovarian:	n/a
49	chr2:183580841-183580891	HNPCEpiC	eye:	n/a
50	chr2:183580829-183580879	HUVEC	blood vessel:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:183502276..183505154-chr2:183507754..183509508,2	K562	blood:
2	chr2:183533406..183536291-chr2:183538994..183541514,2	MCF-7	breast:
3	chr2:183105157..183107059-chr2:183513716..183516271,10	MCF-7	breast:
4	chr2:183568340..183570140-chr2:183571899..183573989,2	K562	blood:
5	chr2:183571018..183573989-chr2:183580764..183583203,2	K562	blood:
6	chr2:183523433..183526191-chr2:183577944..183579909,2	MCF-7	breast:
7	chr2:183530500..183533463-chr2:183581172..183582687,2	MCF-7	breast:
8	chr2:183569800..183572698-chr2:183572719..183574437,2	MCF-7	breast:
9	chr2:183580784..183581354-chr7:35840335..35841333,2	Hela-S3	cervix:
10	chr2:183533406..183536291-chr2:183538994..183541514,2	MCF-7	breast:
11	chr17:57914325..57916942-chr2:183579945..183582060,2	MCF-7	breast:
12	chr2:183165658..183166473-chr2:183513729..183514661,3	MCF-7	breast:
13	chr2:183562956..183565340-chr2:183578999..183580676,2	MCF-7	breast:
14	chr2:183050946..183051551-chr2:183517788..183518340,2	MCF-7	breast:
15	chr2:183050932..183051609-chr2:183514883..183516080,4	MCF-7	breast:
16	chr2:183525253..183526981-chr2:183533807..183535350,2	K562	blood:
17	chr2:183050662..183051405-chr2:183513747..183514396,3	MCF-7	breast:
18	chr2:183562956..183565340-chr2:183578999..183580676,2	MCF-7	breast:
19	chr2:183572976..183576178-chr2:183579194..183582623,4	K562	blood:
20	chr2:182755591..182758830-chr2:183579706..183582403,3	K562	blood:
21	chr2:183568184..183572232-chr2:183575375..183579342,4	K562	blood:
22	chr19:47614665..47616631-chr2:183580076..183582029,2	MCF-7	breast:
23	chr2:182756746..182758830-chr2:183579706..183581743,2	K562	blood:
24	chr2:183516388..183518623-chr2:183519704..183522732,3	K562	blood:
25	chr2:183525253..183526981-chr2:183533807..183535350,2	K562	blood:
26	chr2:183580461..183581050-chr9:132388456..132389164,2	Hela-S3	cervix:
27	chr2:183516388..183518623-chr2:183519704..183522732,3	K562	blood:
28	chr2:183580551..183581074-chr7:100025798..100026773,2	Hela-S3	cervix:
29	chr1:228644091..228645688-chr2:183578348..183580384,2	K562	blood:
30	chr2:183050633..183051569-chr2:183514775..183515804,6	K562	blood:
31	chr2:183570034..183572518-chr2:183580411..183582264,3	K562	blood:
32	chr2:183546308..183548876-chr2:183579294..183581951,2	MCF-7	breast:
33	chr2:183568184..183572232-chr2:183575375..183579342,4	K562	blood:
34	chr2:183561976..183564805-chr2:183566522..183568031,2	K562	blood:
35	chr2:183557913..183559489-chr2:183567582..183569465,2	K562	blood:
36	chr2:183515898..183518111-chr2:183519211..183521393,2	MCF-7	breast:
37	chr2:183569888..183574492-chr2:183579294..183583506,5	MCF-7	breast:
38	chr2:183580425..183582799-chr2:183903051..183904778,2	MCF-7	breast:
39	chr2:183523433..183526191-chr2:183577944..183579909,2	MCF-7	breast:
40	chr2:183568340..183570140-chr2:183571899..183573989,2	K562	blood:
41	chr2:183574014..183578442-chr2:183578822..183583161,9	K562	blood:
42	chr2:183515898..183518111-chr2:183519211..183521393,2	MCF-7	breast:
43	chr2:183569800..183572698-chr2:183572719..183574437,2	MCF-7	breast:
44	chr2:183561976..183564805-chr2:183566522..183568031,2	K562	blood:
45	chr2:183530500..183533463-chr2:183581172..183582687,2	MCF-7	breast:
46	chr2:183580393..183581010-chr7:23144811..23145657,2	Hela-S3	cervix:
47	chr2:183051017..183051535-chr2:183513719..183514634,2	K562	blood:
48	chr2:183564408..183567308-chr2:183580527..183582877,2	K562	blood:
49	chr2:183557913..183559489-chr2:183567582..183569465,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
2	lnc-PDE1A-1	chr2:183537627-183537875	NONHSAT075909
3	lnc-PDE1A-1	chr2:183539151-183539242	XLOC_002420
4	lnc-PDE1A-1	chr2:183539150-183539242	NONHSAT075911
5	lnc-DNAJC10-3	chr2:183513193-183513418	NONHSAT075908
6	lnc-PDE1A-1	chr2:183537302-183537749	NONHSAT075911
7	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
8	lnc-PDE1A-1	chr2:183536804-183536945	XLOC_002420
9	lnc-PDE1A-1	chr2:183537628-183537875	XLOC_002420
10	lnc-PDE1A-1	chr2:183538117-183538135	XLOC_002420
11	lnc-DNAJC10-3	chr2:183510878-183510968	NONHSAT075908
12	lnc-PDE1A-1	chr2:183536803-183536945	NONHSAT075909

No data

Variant related genes	Relation type
DNAJC10	TF binding region
DNAJC10	CpG island
ENSG00000138434	chromatin interactions
ENSG00000148335	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000115252	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000061676	chromatin interactions
ENSG00000122550	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000077232	chromatin interactions
ENSG00000230658	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000130749	chromatin interactions

Extended variants
information (count: 1682 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1682 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10497611	chr2:183508696-183508697	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143336496	chr2:183508748-183508749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187046271	chr2:183508787-183508788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142013857	chr2:183508855-183508856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs67950747	chr2:183508856-183508857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs71008238	chr2:183508886-183508887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200830609	chr2:183508887-183508888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115332364	chr2:183508990-183508991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377238059	chr2:183508991-183508992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs3029371	chr2:183509027-183509028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201652928	chr2:183509028-183509029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79977870	chr2:183509102-183509103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554187218	chr2:183509113-183509114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554221707	chr2:183509118-183509119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551592227	chr2:183509147-183509148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574040619	chr2:183509212-183509213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571410111	chr2:183509304-183509305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10185220	chr2:183509337-183509338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556965494	chr2:183509356-183509357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573692877	chr2:183509433-183509434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72894683	chr2:183509602-183509603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs553081127	chr2:183509624-183509625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572937042	chr2:183509626-183509627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561542907	chr2:183509675-183509676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562027015	chr2:183509712-183509713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs66966503	chr2:183509713-183509714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10211579	chr2:183509741-183509742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs564708676	chr2:183509744-183509745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191836679	chr2:183509751-183509752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10211671	chr2:183509789-183509790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs184074704	chr2:183509805-183509806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529229791	chr2:183509837-183509838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549011655	chr2:183509855-183509856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559581966	chr2:183509871-183509872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565068827	chr2:183509909-183509910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551241010	chr2:183509915-183509916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376916748	chr2:183509930-183509931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10177196	chr2:183509955-183509956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs374735549	chr2:183509964-183509965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537305261	chr2:183509965-183509966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368032887	chr2:183509970-183509971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566927546	chr2:183509992-183509993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113100536	chr2:183510003-183510004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs202242893	chr2:183510004-183510005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187424806	chr2:183510011-183510012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191605590	chr2:183510015-183510016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536246474	chr2:183510064-183510065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182644029	chr2:183510065-183510066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572806959	chr2:183510123-183510124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76458397	chr2:183510136-183510137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183508400-183509000	Enhancers	Muscle Satellite Cultured Cells	--
2	chr2:183509000-183513600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr2:183511800-183512400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:183513600-183513800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr2:183513600-183514200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr2:183513600-183514400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:183513600-183514400	Enhancers	Hela-S3	cervix
8	chr2:183513800-183514000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:183513800-183514200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:183514000-183514200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:183514000-183514200	Enhancers	Fetal Kidney	kidney
12	chr2:183514000-183514200	Enhancers	Osteobl	bone
13	chr2:183514000-183515000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr2:183514000-183515200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:183514200-183515200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr2:183514200-183515200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:183514200-183515200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr2:183514400-183514800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:183514400-183514800	Weak transcription	Hela-S3	cervix
20	chr2:183514800-183515600	Enhancers	Hela-S3	cervix
21	chr2:183514800-183516000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:183515000-183516000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:183515200-183515400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:183515200-183515400	Enhancers	Osteobl	bone
25	chr2:183515200-183515600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:183515200-183515600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:183515200-183516000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr2:183515400-183515600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr2:183515400-183515800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:183515400-183516000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:183515400-183516000	Enhancers	Brain Substantia Nigra	brain
32	chr2:183515600-183519800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:183515800-183516000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:183516800-183517600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr2:183517000-183517400	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr2:183519400-183520800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr2:183519600-183520600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:183519800-183520800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr2:183520200-183520800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:183520200-183521000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr2:183520600-183521000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:183527800-183528200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:183529000-183529600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr2:183531400-183532000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr2:183531800-183532200	Enhancers	Primary B cells from peripheral blood	blood
46	chr2:183532400-183533200	Enhancers	HepG2	liver
47	chr2:183533000-183534000	Bivalent Enhancer	Dnd41	blood
48	chr2:183533200-183533600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr2:183533200-183533600	Flanking Active TSS	HepG2	liver
50	chr2:183533400-183533600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin

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