Variant report

Variant	esv2756954
Chromosome Location	chr2:183528670-183764930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2461)
CpG islands
(count:2076)
Chromatin interactive
region (count:142)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2461 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183679569-183679767	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183668859-183669300	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:183593463-183593469	K562	blood:	n/a	n/a
4	ARID3A	chr2:183649459-183649762	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:183649467-183649783	K562	blood:	n/a	n/a
6	ARID3A	chr2:183755294-183756486	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:183648439-183648583	K562	blood:	n/a	n/a
8	ARID3A	chr2:183731010-183731021	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:183580474-183581183	HepG2	liver:	n/a	n/a
10	ATF1	chr2:183725934-183726010	K562	blood:	n/a	n/a
11	ATF1	chr2:183647473-183647647	K562	blood:	n/a	n/a
12	ATF2	chr2:183580660-183581148	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr2:183580338-183581152	GM12878	blood:	n/a	n/a
14	ATF2	chr2:183580660-183581085	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr2:183580790-183581114	K562	blood:	n/a	chr2:183580978-183580987
16	BACH1	chr2:183580525-183581202	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:183581032-183581106	K562	blood:	n/a	n/a
18	BACH1	chr2:183581406-183581577	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:183730971-183731063	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr2:183732098-183732408	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr2:183591221-183591595	GM12878	blood:	n/a	n/a
22	BATF	chr2:183591303-183591561	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:183683644-183683969	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr2:183580410-183581093	A549	lung:	n/a	chr2:183580912-183580925 chr2:183580685-183580694 chr2:183580748-183580761 chr2:183580903-183580916 chr2:183580753-183580766
25	BCLAF1	chr2:183580322-183581201	GM12878	blood:	n/a	chr2:183580912-183580925 chr2:183580685-183580694 chr2:183580748-183580761 chr2:183580903-183580916 chr2:183580753-183580766
26	BHLHE40	chr2:183583365-183583528	GM12878	blood:	n/a	n/a
27	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
28	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
29	BHLHE40	chr2:183735041-183735273	K562	blood:	n/a	n/a
30	BHLHE40	chr2:183763855-183763984	K562	blood:	n/a	n/a
31	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
32	BHLHE40	chr2:183581895-183581916	GM12878	blood:	n/a	n/a
33	BRCA1	chr2:183732940-183733129	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr2:183731451-183731729	HepG2	liver:	n/a	n/a
35	BRCA1	chr2:183679511-183679776	HepG2	liver:	n/a	n/a
36	BRCA1	chr2:183576504-183576579	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr2:183580850-183581133	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr2:183580727-183581109	HepG2	liver:	n/a	n/a
39	CBX3	chr2:183580321-183581659	K562	blood:	n/a	n/a
40	CCNT2	chr2:183650940-183651109	K562	blood:	n/a	n/a
41	CCNT2	chr2:183735166-183735220	K562	blood:	n/a	n/a
42	CCNT2	chr2:183580601-183581535	K562	blood:	n/a	n/a
43	CEBPB	chr2:183751918-183752113	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:183762393-183762525	A549	lung:	n/a	n/a
45	CEBPB	chr2:183626527-183626940	K562	blood:	n/a	chr2:183626725-183626736
46	CEBPB	chr2:183626539-183626936	IMR90	lung:	n/a	chr2:183626725-183626736
47	CEBPB	chr2:183623124-183623454	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:183731324-183731676	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:183756383-183756726	IMR90	lung:	n/a	chr2:183756554-183756567 chr2:183756555-183756566 chr2:183756554-183756567
50	CEBPB	chr2:183558969-183559251	IMR90	lung:	n/a	chr2:183559095-183559106

(count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183580818-183580868	GM06990	blood:	n/a
2	chr2:183731599-183731649	AG09319	gingival:	n/a
3	chr2:183580818-183580868	GM06990	blood:	n/a
4	chr2:183731599-183731649	AG09319	gingival:	n/a
5	chr2:183580841-183580891	GM12891	blood:	n/a
6	chr2:183731407-183731457	SK-N-SH	brain:	n/a
7	chr2:183731676-183731726	MCF-7	breast:	n/a
8	chr2:183580574-183580624	NHBE	bronchial:	n/a
9	chr2:183729189-183729239	GM12878	blood:	n/a
10	chr2:183731676-183731726	HCPEpiC	choroid plexus:	n/a
11	chr2:183658977-183659027	CMK	blood:	n/a
12	chr2:183642235-183642285	BJ	skin:	n/a
13	chr2:183577625-183577675	LNCaP	prostate:	n/a
14	chr2:183577625-183577675	U87	brain:	n/a
15	chr2:183732607-183732657	H1-hESC	embryonic stem cell:	embryo
16	chr2:183731169-183731219	Hepatocyte	liver:	n/a
17	chr2:183731599-183731649	GM06990	blood:	n/a
18	chr2:183580463-183580513	AG04449	skin:	fetal
19	chr2:183731169-183731219	HCT-116	colon:	n/a
20	chr2:183683268-183683318	HMEC	breast:	n/a
21	chr2:183580829-183580879	PFSK-1	brain:	n/a
22	chr2:183731832-183731882	BJ	skin:	n/a
23	chr2:183699153-183699203	GM19239	blood:	n/a
24	chr2:183683268-183683318	HUVEC	blood vessel:	n/a
25	chr2:183580818-183580868	HRPEpiC	eye:	n/a
26	chr2:183730940-183730990	MCF-7	breast:	n/a
27	chr2:183699153-183699203	ProgFib	skin:	n/a
28	chr2:183731169-183731219	GM12891	blood:	n/a
29	chr2:183580463-183580513	Jurkat	blood:	n/a
30	chr2:183723096-183723146	T-47D	breast:	n/a
31	chr2:183731563-183731613	K562	blood:	n/a
32	chr2:183580818-183580868	AoSMC	blood vessel:	n/a
33	chr2:183580463-183580513	U87	brain:	n/a
34	chr2:183723096-183723146	CMK	blood:	n/a
35	chr2:183580523-183580573	GM12878	blood:	n/a
36	chr2:183580841-183580891	HCPEpiC	choroid plexus:	n/a
37	chr2:183732607-183732657	ProgFib	skin:	n/a
38	chr2:183731824-183731874	BE2_C	brain:	n/a
39	chr2:183580463-183580513	NHDF-neo	bronchial:	n/a
40	chr2:183580910-183580960	Caco-2	colon:	n/a
41	chr2:183580463-183580513	HEEpiC	esophagus:	n/a
42	chr2:183732062-183732112	NB4	blood:	n/a
43	chr2:183731563-183731613	BE2_C	brain:	n/a
44	chr2:183732062-183732112	SKMC	muscle:	n/a
45	chr2:183580694-183580744	CMK	blood:	n/a
46	chr2:183733105-183733155	U87	brain:	n/a
47	chr2:183731169-183731219	Caco-2	colon:	n/a
48	chr2:183667124-183667174	GM12892	blood:	n/a
49	chr2:183580950-183581000	AoSMC	blood vessel:	n/a
50	chr2:183580463-183580513	MCF10A-Er-Src	breast:	n/a

(count:142 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:183525253..183526981-chr2:183533807..183535350,2	K562	blood:
2	chr2:183691013..183692579-chr2:183710091..183711908,2	MCF-7	breast:
3	chr2:183600722..183602612-chr2:183608045..183610895,3	K562	blood:
4	chr2:183622731..183624252-chr2:183625888..183627970,2	K562	blood:
5	chr2:183598485..183600408-chr2:183608277..183611050,2	MCF-7	breast:
6	chr2:183570034..183572518-chr2:183580411..183582264,3	K562	blood:
7	chr2:183574014..183578442-chr2:183578822..183583161,9	K562	blood:
8	chr2:183579526..183582519-chr2:183598356..183600848,2	K562	blood:
9	chr2:183591742..183594215-chr2:183596337..183599496,3	MCF-7	breast:
10	chr2:183580461..183581050-chr9:132388456..132389164,2	Hela-S3	cervix:
11	chr2:183676835..183678660-chr2:183680847..183683198,2	K562	blood:
12	chr2:183759211..183762247-chr2:183762468..183766311,3	K562	blood:
13	chr2:183659213..183661128-chr2:183664377..183666463,2	MCF-7	breast:
14	chr2:183658306..183660291-chr2:183661982..183664789,2	K562	blood:
15	chr2:183676117..183678247-chr2:183702144..183703855,2	MCF-7	breast:
16	chr2:183618431..183622157-chr2:183625093..183627097,3	K562	blood:
17	chr2:183568184..183572232-chr2:183575375..183579342,4	K562	blood:
18	chr2:183533406..183536291-chr2:183538994..183541514,2	MCF-7	breast:
19	chr2:183580393..183581010-chr7:23144811..23145657,2	Hela-S3	cervix:
20	chr2:183598562..183601239-chr2:183604490..183606088,2	K562	blood:
21	chr2:183596118..183599197-chr2:183620167..183622183,3	K562	blood:
22	chr2:183569800..183572698-chr2:183572719..183574437,2	MCF-7	breast:
23	chr2:183666474..183669367-chr2:183675559..183677309,2	K562	blood:
24	chr2:183750442..183752210-chr2:183755879..183757846,2	K562	blood:
25	chr2:183579405..183581877-chr2:183597758..183599886,2	MCF-7	breast:
26	chr2:183601411..183603904-chr2:183956963..183959592,2	MCF-7	breast:
27	chr2:183569800..183572698-chr2:183572719..183574437,2	MCF-7	breast:
28	chr2:183758074..183761061-chr2:183762442..183764748,3	MCF-7	breast:
29	chr2:183530500..183533463-chr2:183581172..183582687,2	MCF-7	breast:
30	chr2:183668592..183670850-chr2:183672599..183674882,2	K562	blood:
31	chr2:183706094..183709034-chr2:183715040..183717717,2	K562	blood:
32	chr2:183664890..183667245-chr2:183673485..183675403,2	K562	blood:
33	chr2:183533406..183536291-chr2:183538994..183541514,2	MCF-7	breast:
34	chr2:183562956..183565340-chr2:183578999..183580676,2	MCF-7	breast:
35	chr2:183546308..183548876-chr2:183579294..183581951,2	MCF-7	breast:
36	chr2:183668592..183670850-chr2:183672599..183674882,2	K562	blood:
37	chr2:183736856..183738517-chr2:183740289..183742919,2	MCF-7	breast:
38	chr2:183600722..183602612-chr2:183608045..183610895,3	K562	blood:
39	chr2:183660311..183663383-chr2:183663723..183666825,3	K562	blood:
40	chr17:57914325..57916942-chr2:183579945..183582060,2	MCF-7	breast:
41	chr2:183648162..183650730-chr2:183663988..183666770,2	K562	blood:
42	chr2:183691773..183694607-chr2:183701839..183703890,2	K562	blood:
43	chr2:183603082..183605652-chr2:183608398..183611324,2	K562	blood:
44	chr2:183605695..183607908-chr2:183711047..183713446,2	K562	blood:
45	chr2:183752548..183754823-chr2:183756546..183759081,2	K562	blood:
46	chr2:183585145..183587372-chr2:183598804..183601047,2	K562	blood:
47	chr2:183572976..183576178-chr2:183579194..183582623,4	K562	blood:
48	chr2:183615250..183618246-chr2:183622533..183624342,2	K562	blood:
49	chr2:183616174..183617713-chr2:183625030..183626585,2	MCF-7	breast:
50	chr2:183628146..183628821-chr2:183844437..183845367,4	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DUSP19-4	chr2:183650679-183652638	NONHSAT075919
2	lnc-DUSP19-3	chr2:183652825-183653162	NONHSAT075920
3	lnc-PDE1A-1	chr2:183537628-183537875	XLOC_002420
4	lnc-DNAJC10-2	chr2:183654087-183659706	NONHSAT075921
5	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
6	lnc-PDE1A-1	chr2:183536803-183536945	NONHSAT075909
7	lnc-PDE1A-1	chr2:183538117-183538135	XLOC_002420
8	lnc-PDE1A-1	chr2:183536804-183536945	XLOC_002420
9	lnc-PDE1A-1	chr2:183539151-183539242	XLOC_002420
10	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
11	lnc-PDE1A-1	chr2:183537302-183537749	NONHSAT075911
12	lnc-PDE1A-1	chr2:183539150-183539242	NONHSAT075911
13	lnc-PDE1A-1	chr2:183537627-183537875	NONHSAT075909

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	FRZB	hsa-miR-30b-5p	chr2:183699473-183699467
2	FRZB	hsa-miR-30b-5p	chr2:183699467-183699488
3	FRZB	hsa-miR-30b-5p	chr2:183699080-183699101

Variant related genes	Relation type
FRZB	TF binding region
RPL31P15	TF binding region
ENSG00000212404	TF binding region
DNAJC10	TF binding region
RNU6-1122P	TF binding region
FRZB	CpG island
RPL31P15	CpG island
ENSG00000212404	CpG island
DNAJC10	CpG island
RNU6-1122P	CpG island
ENSG00000062716	chromatin interactions
ENSG00000122550	chromatin interactions
ENSG00000148335	chromatin interactions
ENSG00000232430	chromatin interactions
ENSG00000212404	chromatin interactions
ENSG00000230658	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000138434	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000077232	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000061676	chromatin interactions
ENSG00000130749	chromatin interactions
ENSG00000146834	chromatin interactions

Extended variants
information (count: 7835 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:7835 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2696113	chr2:183529071-183529072	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs180960272	chr2:183529101-183529102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542851431	chr2:183529137-183529138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527332985	chr2:183529138-183529139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559642154	chr2:183529186-183529187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528420091	chr2:183529224-183529225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544956909	chr2:183529254-183529255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564712420	chr2:183529272-183529273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138412899	chr2:183529275-183529276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550402192	chr2:183529283-183529284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567063750	chr2:183529289-183529290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546972497	chr2:183529292-183529293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529406788	chr2:183529294-183529295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549187385	chr2:183529301-183529302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565998067	chr2:183529309-183529310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2578002	chr2:183529310-183529311	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs544679621	chr2:183529318-183529319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17356699	chr2:183529352-183529353	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs185377196	chr2:183529361-183529362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569391733	chr2:183529434-183529435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537490279	chr2:183529474-183529475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143897561	chr2:183529512-183529513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565590044	chr2:183529516-183529517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574186678	chr2:183529550-183529551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368452824	chr2:183529575-183529576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542818853	chr2:183529582-183529583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553220561	chr2:183529584-183529585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72625274	chr2:183531424-183531425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2971890	chr2:183531464-183531465	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs7601851	chr2:183531538-183531539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201571305	chr2:183531539-183531540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552416700	chr2:183531551-183531552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376313134	chr2:183531592-183531593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79951203	chr2:183531611-183531612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11903253	chr2:183531639-183531640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs188637311	chr2:183531664-183531665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs55695415	chr2:183531674-183531675	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs56396309	chr2:183531677-183531678	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553747666	chr2:183531699-183531700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192977759	chr2:183531729-183531730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35730061	chr2:183531818-183531819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545865233	chr2:183531877-183531878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556035228	chr2:183531898-183531899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35171778	chr2:183532081-183532082	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs544829962	chr2:183532108-183532109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115808389	chr2:183532117-183532118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530439505	chr2:183532128-183532129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540961251	chr2:183532192-183532193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527989788	chr2:183532428-183532429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552630237	chr2:183532456-183532457	Enhancers	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:3400 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183529000-183529600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr2:183531400-183532000	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr2:183531800-183532200	Enhancers	Primary B cells from peripheral blood	blood
4	chr2:183532400-183533200	Enhancers	HepG2	liver
5	chr2:183533000-183534000	Bivalent Enhancer	Dnd41	blood
6	chr2:183533200-183533600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:183533200-183533600	Flanking Active TSS	HepG2	liver
8	chr2:183533400-183533600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:183533400-183533800	Enhancers	Esophagus	oesophagus
10	chr2:183533400-183534000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:183533400-183534800	Enhancers	Pancreas	Pancrea
12	chr2:183533600-183534400	Enhancers	HepG2	liver
13	chr2:183533600-183537400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:183534000-183534400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:183534400-183534800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:183534800-183537400	Weak transcription	Pancreas	Pancrea
17	chr2:183537000-183538000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:183537000-183538000	Enhancers	NH-A	brain
19	chr2:183537200-183537600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:183537200-183537600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:183537200-183537600	Enhancers	HSMM	muscle
22	chr2:183537200-183537800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:183537200-183537800	Enhancers	NHDF-Ad	bronchial
24	chr2:183537200-183538000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr2:183537200-183538000	Enhancers	HUVEC	blood vessel
26	chr2:183537200-183538000	Enhancers	NHLF	lung
27	chr2:183537200-183538000	Enhancers	Osteobl	bone
28	chr2:183537200-183538200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:183537400-183537600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr2:183537400-183537800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:183537400-183537800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:183537400-183537800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:183537400-183537800	Enhancers	Fetal Heart	heart
34	chr2:183537400-183537800	Enhancers	Pancreas	Pancrea
35	chr2:183537400-183538000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:183537400-183538000	Enhancers	Hela-S3	cervix
37	chr2:183537400-183538000	Enhancers	NHEK	skin
38	chr2:183544200-183545400	Weak transcription	Brain Cingulate Gyrus	brain
39	chr2:183544400-183546800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr2:183544600-183548200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr2:183546800-183547400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr2:183546800-183547400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr2:183546800-183547600	Enhancers	Primary B cells from peripheral blood	blood
44	chr2:183546800-183547800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr2:183546800-183547800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:183547000-183547600	Enhancers	Adipose Nuclei	Adipose
47	chr2:183547400-183547800	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr2:183551200-183551800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
49	chr2:183559000-183559400	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr2:183563400-183563800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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