Variant report

Variant	nsv875483
Chromosome Location	chr2:183537399-183657867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1486)
CpG islands
(count:856)
Chromatin interactive
region (count:87)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1486 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183580474-183581183	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183649459-183649762	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:183648439-183648583	K562	blood:	n/a	n/a
4	ARID3A	chr2:183593463-183593469	K562	blood:	n/a	n/a
5	ARID3A	chr2:183649467-183649783	K562	blood:	n/a	n/a
6	ATF1	chr2:183647473-183647647	K562	blood:	n/a	n/a
7	ATF2	chr2:183580660-183581085	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr2:183580660-183581148	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:183580338-183581152	GM12878	blood:	n/a	n/a
10	ATF3	chr2:183580790-183581114	K562	blood:	n/a	chr2:183580978-183580987
11	BACH1	chr2:183581032-183581106	K562	blood:	n/a	n/a
12	BACH1	chr2:183581406-183581577	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr2:183580525-183581202	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr2:183591303-183591561	GM12878	blood:	n/a	n/a
15	BATF	chr2:183591221-183591595	GM12878	blood:	n/a	n/a
16	BCL3	chr2:183580410-183581093	A549	lung:	n/a	chr2:183580912-183580925 chr2:183580685-183580694 chr2:183580748-183580761 chr2:183580903-183580916 chr2:183580753-183580766
17	BCLAF1	chr2:183580322-183581201	GM12878	blood:	n/a	chr2:183580912-183580925 chr2:183580685-183580694 chr2:183580748-183580761 chr2:183580903-183580916 chr2:183580753-183580766
18	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
19	BHLHE40	chr2:183581895-183581916	GM12878	blood:	n/a	n/a
20	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
21	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
22	BHLHE40	chr2:183583365-183583528	GM12878	blood:	n/a	n/a
23	BRCA1	chr2:183580727-183581109	HepG2	liver:	n/a	n/a
24	BRCA1	chr2:183580850-183581133	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr2:183576504-183576579	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr2:183580321-183581659	K562	blood:	n/a	n/a
27	CCNT2	chr2:183650940-183651109	K562	blood:	n/a	n/a
28	CCNT2	chr2:183580601-183581535	K562	blood:	n/a	n/a
29	CEBPB	chr2:183626557-183626827	K562	blood:	n/a	chr2:183626725-183626736
30	CEBPB	chr2:183626593-183626901	HepG2	liver:	n/a	chr2:183626725-183626736
31	CEBPB	chr2:183623123-183623469	A549	lung:	n/a	n/a
32	CEBPB	chr2:183594396-183594788	HepG2	liver:	n/a	chr2:183594620-183594631
33	CEBPB	chr2:183623136-183623452	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:183626520-183626953	K562	blood:	n/a	chr2:183626725-183626736
35	CEBPB	chr2:183626474-183626883	MCF-7	breast:	n/a	chr2:183626725-183626736
36	CEBPB	chr2:183558920-183559274	HepG2	liver:	n/a	chr2:183559095-183559106
37	CEBPB	chr2:183626566-183626949	HepG2	liver:	n/a	chr2:183626725-183626736
38	CEBPB	chr2:183623124-183623454	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:183626517-183626973	ECC-1	luminal epithelium:	n/a	chr2:183626725-183626736
40	CEBPB	chr2:183626540-183626927	A549	lung:	n/a	chr2:183626725-183626736
41	CEBPB	chr2:183580798-183580804	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:183546942-183547197	K562	blood:	n/a	n/a
43	CEBPB	chr2:183651455-183651655	A549	lung:	n/a	n/a
44	CEBPB	chr2:183626550-183626916	H1-hESC	embryonic stem cell:	n/a	chr2:183626725-183626736
45	CEBPB	chr2:183623298-183623480	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr2:183626539-183626936	IMR90	lung:	n/a	chr2:183626725-183626736
47	CEBPB	chr2:183647103-183647312	HepG2	liver:	n/a	chr2:183647245-183647256
48	CEBPB	chr2:183626527-183626940	K562	blood:	n/a	chr2:183626725-183626736
49	CEBPB	chr2:183623126-183623467	K562	blood:	n/a	n/a
50	CEBPB	chr2:183626538-183626940	HCT-116	colon:	n/a	chr2:183626725-183626736

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183580523-183580573	Hela-S3	cervix:	n/a
2	chr2:183580829-183580879	ovcar-3	ovarian:	n/a
3	chr2:183580523-183580573	Hela-S3	cervix:	n/a
4	chr2:183580829-183580879	ovcar-3	ovarian:	n/a
5	chr2:183577625-183577675	NB4	blood:	n/a
6	chr2:183580523-183580573	GM12878	blood:	n/a
7	chr2:183580841-183580891	U87	brain:	n/a
8	chr2:183580574-183580624	HRCEpiC	kidney:	n/a
9	chr2:183580910-183580960	AG04449	skin:	fetal
10	chr2:183580818-183580868	GM19239	blood:	n/a
11	chr2:183580523-183580573	IMR90	lung:	fetal
12	chr2:183580818-183580868	SKMC	muscle:	n/a
13	chr2:183580910-183580960	Caco-2	colon:	n/a
14	chr2:183580818-183580868	HCM	heart:	n/a
15	chr2:183580910-183580960	Jurkat	blood:	n/a
16	chr2:183580829-183580879	GM06990	blood:	n/a
17	chr2:183584043-183584093	NH-A	brain:	n/a
18	chr2:183581591-183581641	NHDF-neo	bronchial:	n/a
19	chr2:183580523-183580573	HRPEpiC	eye:	n/a
20	chr2:183642235-183642285	HUVEC	blood vessel:	n/a
21	chr2:183580950-183581000	Caco-2	colon:	n/a
22	chr2:183642235-183642285	NT2-D1	testis:	n/a
23	chr2:183642235-183642285	HepG2	liver:	n/a
24	chr2:183580829-183580879	GM12878	blood:	n/a
25	chr2:183577625-183577675	HAEpiC	amniotic membrane:	n/a
26	chr2:183580829-183580879	RPTEC	kidney:	n/a
27	chr2:183581591-183581641	HEEpiC	esophagus:	n/a
28	chr2:183577625-183577675	AG09309	skin:	n/a
29	chr2:183580906-183580956	BJ	skin:	n/a
30	chr2:183581591-183581641	H1-hESC	embryonic stem cell:	embryo
31	chr2:183642235-183642285	AG09309	skin:	n/a
32	chr2:183580910-183580960	HRPEpiC	eye:	n/a
33	chr2:183580841-183580891	HCT-116	colon:	n/a
34	chr2:183577625-183577675	SK-N-SH	brain:	n/a
35	chr2:183580910-183580960	ovcar-3	ovarian:	n/a
36	chr2:183642235-183642285	HNPCEpiC	eye:	n/a
37	chr2:183580950-183581000	U87	brain:	n/a
38	chr2:183580694-183580744	A549	lung:	n/a
39	chr2:183580463-183580513	HIPEpiC	eye:	n/a
40	chr2:183580950-183581000	T-47D	breast:	n/a
41	chr2:183580950-183581000	RPTEC	kidney:	n/a
42	chr2:183580829-183580879	H1-hESC	embryonic stem cell:	embryo
43	chr2:183580829-183580879	K562	blood:	n/a
44	chr2:183580818-183580868	SK-N-MC	brain:	n/a
45	chr2:183580463-183580513	K562	blood:	n/a
46	chr2:183581591-183581641	A549	lung:	n/a
47	chr2:183580829-183580879	HIPEpiC	eye:	n/a
48	chr2:183577625-183577675	IMR90	lung:	fetal
49	chr2:183581591-183581641	GM12891	blood:	n/a
50	chr2:183642235-183642285	NB4	blood:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:183598562..183601239-chr2:183604490..183606088,2	K562	blood:
2	chr2:183592791..183595028-chr2:183604249..183606530,2	K562	blood:
3	chr2:183600722..183602612-chr2:183608045..183610895,3	K562	blood:
4	chr2:183568184..183572232-chr2:183575375..183579342,4	K562	blood:
5	chr2:183587075..183588639-chr2:183597814..183600510,2	MCF-7	breast:
6	chr2:183618431..183622157-chr2:183625093..183627097,3	K562	blood:
7	chr2:183615250..183618246-chr2:183622533..183624342,2	K562	blood:
8	chr2:183615250..183618246-chr2:183622533..183624342,2	K562	blood:
9	chr2:183598869..183601540-chr2:183602374..183605129,3	MCF-7	breast:
10	chr2:183580389..183583090-chr2:183602955..183604552,2	MCF-7	breast:
11	chr2:183591742..183594215-chr2:183596337..183599496,3	MCF-7	breast:
12	chr2:183603082..183605652-chr2:183608398..183611324,2	K562	blood:
13	chr2:183568184..183572232-chr2:183575375..183579342,4	K562	blood:
14	chr2:183564408..183567308-chr2:183580527..183582877,2	K562	blood:
15	chr2:183579924..183582324-chr2:183596342..183598090,2	MCF-7	breast:
16	chr2:183585145..183587372-chr2:183598804..183601047,2	K562	blood:
17	chr2:183580551..183581074-chr7:100025798..100026773,2	Hela-S3	cervix:
18	chr2:183648162..183650730-chr2:183663988..183666770,2	K562	blood:
19	chr2:183579751..183583297-chr2:183584995..183591341,8	MCF-7	breast:
20	chr2:183616174..183617713-chr2:183625030..183626585,2	MCF-7	breast:
21	chr2:183598485..183600408-chr2:183608277..183611050,2	MCF-7	breast:
22	chr2:183523433..183526191-chr2:183577944..183579909,2	MCF-7	breast:
23	chr2:183618431..183622157-chr2:183625093..183627097,3	K562	blood:
24	chr2:183616174..183617713-chr2:183625030..183626585,2	MCF-7	breast:
25	chr2:183570034..183572518-chr2:183580411..183582264,3	K562	blood:
26	chr2:183580659..183582822-chr2:183604202..183605907,2	K562	blood:
27	chr2:183622731..183624252-chr2:183625888..183627970,2	K562	blood:
28	chr2:183600490..183602060-chr2:183603873..183605839,2	K562	blood:
29	chr2:183530500..183533463-chr2:183581172..183582687,2	MCF-7	breast:
30	chr2:183580393..183581010-chr7:23144811..23145657,2	Hela-S3	cervix:
31	chr2:183589155..183591110-chr2:183597829..183599680,2	K562	blood:
32	chr2:183598562..183601239-chr2:183604490..183606088,2	K562	blood:
33	chr2:183572976..183576178-chr2:183579194..183582623,4	K562	blood:
34	chr2:183557913..183559489-chr2:183567582..183569465,2	K562	blood:
35	chr2:183569800..183572698-chr2:183572719..183574437,2	MCF-7	breast:
36	chr2:183579077..183581279-chr2:183626504..183629491,2	K562	blood:
37	chr2:183579526..183582484-chr2:183598917..183600848,2	K562	blood:
38	chr2:183579526..183582519-chr2:183598356..183600848,2	K562	blood:
39	chr2:183600490..183602060-chr2:183603873..183605839,2	K562	blood:
40	chr2:183546308..183548876-chr2:183579294..183581951,2	MCF-7	breast:
41	chr2:183615854..183617746-chr2:183618708..183621163,2	K562	blood:
42	chr2:183562956..183565340-chr2:183578999..183580676,2	MCF-7	breast:
43	chr2:183587075..183588639-chr2:183597814..183600510,2	MCF-7	breast:
44	chr2:183561976..183564805-chr2:183566522..183568031,2	K562	blood:
45	chr2:183619535..183621999-chr2:183651493..183653388,2	K562	blood:
46	chr2:183562956..183565340-chr2:183578999..183580676,2	MCF-7	breast:
47	chr2:183580042..183581600-chr2:183608683..183611229,2	MCF-7	breast:
48	chr2:183648396..183651176-chr2:183657370..183660801,3	K562	blood:
49	chr2:183591742..183594215-chr2:183596337..183599496,3	MCF-7	breast:
50	chr2:183569888..183574492-chr2:183579294..183583506,5	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE1A-1	chr2:183539151-183539242	XLOC_002420
2	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
3	lnc-DNAJC10-2	chr2:183654087-183659706	NONHSAT075921
4	lnc-PDE1A-1	chr2:183537627-183537875	NONHSAT075909
5	lnc-DUSP19-4	chr2:183650679-183652638	NONHSAT075919
6	lnc-PDE1A-1	chr2:183537628-183537875	XLOC_002420
7	lnc-PDE1A-1	chr2:183539150-183539242	NONHSAT075911
8	lnc-PDE1A-1	chr2:183537302-183537749	NONHSAT075911
9	lnc-PDE1A-1	chr2:183538117-183538135	XLOC_002420
10	lnc-DUSP19-3	chr2:183652825-183653162	NONHSAT075920
11	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420

No data

Variant related genes	Relation type
RPL31P15	TF binding region
DNAJC10	TF binding region
RPL31P15	CpG island
DNAJC10	CpG island
ENSG00000062716	chromatin interactions
ENSG00000148335	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000138434	chromatin interactions
ENSG00000232430	chromatin interactions
ENSG00000122550	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000061676	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000230658	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000077232	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000130749	chromatin interactions

Extended variants
information (count: 3948 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3948 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs825662	chr2:183537399-183537400	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34410333	chr2:183537586-183537587	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs566863274	chr2:183537680-183537681	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs532304243	chr2:183537693-183537694	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs146297919	chr2:183537749-183537750	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs76880926	chr2:183537777-183537778	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs537722443	chr2:183537809-183537810	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs554488860	chr2:183537816-183537817	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs138805701	chr2:183537867-183537868	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs185018783	chr2:183537871-183537872	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs825661	chr2:183537895-183537896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149369093	chr2:183537898-183537899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557142635	chr2:183537902-183537903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576887919	chr2:183537909-183537910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs57829961	chr2:183537920-183537921	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs189095811	chr2:183537937-183537938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77479712	chr2:183537950-183537951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143770230	chr2:183538014-183538015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73975511	chr2:183538018-183538019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186556302	chr2:183538118-183538119	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs565231728	chr2:183538121-183538122	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs540288536	chr2:183538145-183538146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148149361	chr2:183538155-183538156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369124167	chr2:183538172-183538173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191038581	chr2:183539150-183539151	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs548428135	chr2:183539170-183539171	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs140176034	chr2:183539173-183539174	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs572713091	chr2:183539176-183539177	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs372934390	chr2:183539183-183539184	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs71427861	chr2:183544207-183544208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573523922	chr2:183544223-183544224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145086353	chr2:183544224-183544225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11903020	chr2:183544235-183544236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs575665228	chr2:183544238-183544239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544303665	chr2:183544269-183544270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535136237	chr2:183544311-183544312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555318064	chr2:183544394-183544395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530123535	chr2:183544409-183544410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547102916	chr2:183544427-183544428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559914994	chr2:183544432-183544433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139028689	chr2:183544435-183544436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552004395	chr2:183544484-183544485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568831563	chr2:183544593-183544594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535277878	chr2:183544603-183544604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547861218	chr2:183544629-183544630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568074222	chr2:183544637-183544638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533647139	chr2:183544713-183544714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564943575	chr2:183544752-183544753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552704720	chr2:183544853-183544854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539238070	chr2:183544878-183544879	Enhancers 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:2364 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183533600-183537400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:183534800-183537400	Weak transcription	Pancreas	Pancrea
3	chr2:183537000-183538000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:183537000-183538000	Enhancers	NH-A	brain
5	chr2:183537200-183537600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:183537200-183537600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:183537200-183537600	Enhancers	HSMM	muscle
8	chr2:183537200-183537800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:183537200-183537800	Enhancers	NHDF-Ad	bronchial
10	chr2:183537200-183538000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:183537200-183538000	Enhancers	HUVEC	blood vessel
12	chr2:183537200-183538000	Enhancers	NHLF	lung
13	chr2:183537200-183538000	Enhancers	Osteobl	bone
14	chr2:183537200-183538200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr2:183537400-183537600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:183537400-183537800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr2:183537400-183537800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:183537400-183537800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:183537400-183537800	Enhancers	Fetal Heart	heart
20	chr2:183537400-183537800	Enhancers	Pancreas	Pancrea
21	chr2:183537400-183538000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:183537400-183538000	Enhancers	Hela-S3	cervix
23	chr2:183537400-183538000	Enhancers	NHEK	skin
24	chr2:183544200-183545400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr2:183544400-183546800	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr2:183544600-183548200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr2:183546800-183547400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr2:183546800-183547400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr2:183546800-183547600	Enhancers	Primary B cells from peripheral blood	blood
30	chr2:183546800-183547800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:183546800-183547800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr2:183547000-183547600	Enhancers	Adipose Nuclei	Adipose
33	chr2:183547400-183547800	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr2:183551200-183551800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr2:183559000-183559400	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr2:183563400-183563800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:183569000-183571000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr2:183569400-183571000	Enhancers	Primary hematopoietic stem cells	blood
39	chr2:183569400-183571000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr2:183569600-183571000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr2:183570000-183570600	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr2:183570200-183570600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr2:183570600-183571000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr2:183571200-183571600	Enhancers	Brain Substantia Nigra	brain
45	chr2:183571400-183571600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr2:183577200-183580000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr2:183577400-183578200	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr2:183577600-183577800	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr2:183577600-183578000	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr2:183577600-183579600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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