Variant report

Variant	nsv1008230
Chromosome Location	chr2:186474069-186818718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1406)
CpG islands
(count:550)
Chromatin interactive
region (count:58)
LncRNA
region (count:42)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:186766781-186767039	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:186678380-186678904	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:186603689-186603907	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:186510210-186510829	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:186756102-186757040	HepG2	liver:	n/a	n/a
6	ATF1	chr2:186693024-186693115	K562	blood:	n/a	n/a
7	ATF1	chr2:186586784-186586978	K562	blood:	n/a	n/a
8	ATF2	chr2:186509544-186509954	GM12878	blood:	n/a	n/a
9	ATF2	chr2:186603605-186603967	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:186603621-186603950	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr2:186603273-186603956	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr2:186698786-186698866	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr2:186650918-186651197	GM12878	blood:	n/a	chr2:186651050-186651061
14	BATF	chr2:186650911-186651150	GM12878	blood:	n/a	chr2:186651050-186651061
15	BATF	chr2:186509574-186509959	GM12878	blood:	n/a	n/a
16	BATF	chr2:186661618-186661923	GM12878	blood:	n/a	n/a
17	BCLAF1	chr2:186509649-186509904	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:186591465-186591564	HepG2	liver:	n/a	n/a
19	BHLHE40	chr2:186678411-186678682	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:186678327-186678780	HepG2	liver:	n/a	n/a
21	BHLHE40	chr2:186603670-186603870	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:186678322-186678854	HepG2	liver:	n/a	n/a
23	BHLHE40	chr2:186727838-186727908	K562	blood:	n/a	n/a
24	BHLHE40	chr2:186603836-186603843	K562	blood:	n/a	n/a
25	BRCA1	chr2:186775907-186775908	GM12878	blood:	n/a	n/a
26	BRCA1	chr2:186603755-186603918	HepG2	liver:	n/a	n/a
27	BRCA1	chr2:186603628-186603971	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr2:186603562-186604004	K562	blood:	n/a	n/a
29	CBX3	chr2:186700648-186700857	K562	blood:	n/a	n/a
30	CBX3	chr2:186554740-186555339	HCT-116	colon:	n/a	n/a
31	CBX3	chr2:186554778-186555281	HCT-116	colon:	n/a	n/a
32	CCNT2	chr2:186798987-186799212	K562	blood:	n/a	n/a
33	CCNT2	chr2:186508599-186508741	K562	blood:	n/a	n/a
34	CCNT2	chr2:186663343-186663462	K562	blood:	n/a	n/a
35	CCNT2	chr2:186603668-186603984	K562	blood:	n/a	n/a
36	CEBPB	chr2:186663341-186664155	HepG2	liver:	n/a	chr2:186663973-186663984
37	CEBPB	chr2:186478710-186478888	A549	lung:	n/a	chr2:186478732-186478743
38	CEBPB	chr2:186533467-186533798	Hela-S3	cervix:	n/a	chr2:186533645-186533656
39	CEBPB	chr2:186510221-186510640	HepG2	liver:	n/a	chr2:186510394-186510405
40	CEBPB	chr2:186724386-186724600	K562	blood:	n/a	n/a
41	CEBPB	chr2:186478620-186478884	HepG2	liver:	n/a	chr2:186478732-186478743
42	CEBPB	chr2:186535082-186535227	HepG2	liver:	n/a	chr2:186535119-186535130
43	CEBPB	chr2:186689277-186689483	A549	lung:	n/a	n/a
44	CEBPB	chr2:186603510-186603988	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr2:186533506-186533791	A549	lung:	n/a	chr2:186533645-186533656
46	CEBPB	chr2:186719492-186720096	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr2:186680248-186680252	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:186688718-186689043	HepG2	liver:	n/a	chr2:186688892-186688903
49	CEBPB	chr2:186703330-186703591	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:186533508-186533786	H1-hESC	embryonic stem cell:	n/a	chr2:186533645-186533656

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186609566-186609616	AG04450	lung:	fetal
2	chr2:186609566-186609616	AG04450	lung:	fetal
3	chr2:186603398-186603448	CMK	blood:	n/a
4	chr2:186603441-186603491	GM19239	blood:	n/a
5	chr2:186727863-186727913	SKMC	muscle:	n/a
6	chr2:186610279-186610329	HCPEpiC	choroid plexus:	n/a
7	chr2:186727863-186727913	NHDF-neo	bronchial:	n/a
8	chr2:186610279-186610329	HIPEpiC	eye:	n/a
9	chr2:186727863-186727913	HCF	heart:	n/a
10	chr2:186610279-186610329	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:186603398-186603448	BE2_C	brain:	n/a
12	chr2:186609566-186609616	PANC-1	pancreas:	n/a
13	chr2:186603981-186604031	SAEC	small airway:	n/a
14	chr2:186601802-186601852	LNCaP	prostate:	n/a
15	chr2:186603561-186603611	HepG2	liver:	n/a
16	chr2:186610279-186610329	NH-A	brain:	n/a
17	chr2:186603639-186603689	CMK	blood:	n/a
18	chr2:186603639-186603689	ovcar-3	ovarian:	n/a
19	chr2:186601802-186601852	SK-N-SH	brain:	n/a
20	chr2:186609566-186609616	Jurkat	blood:	n/a
21	chr2:186609566-186609616	A549	lung:	n/a
22	chr2:186603441-186603491	RPTEC	kidney:	n/a
23	chr2:186603639-186603689	PANC-1	pancreas:	n/a
24	chr2:186603639-186603689	HAEpiC	amniotic membrane:	n/a
25	chr2:186603441-186603491	HCF	heart:	n/a
26	chr2:186603639-186603689	NHBE	bronchial:	n/a
27	chr2:186603441-186603491	PFSK-1	brain:	n/a
28	chr2:186727863-186727913	Caco-2	colon:	n/a
29	chr2:186601802-186601852	AG04449	skin:	fetal
30	chr2:186603561-186603611	H1-hESC	embryonic stem cell:	embryo
31	chr2:186603981-186604031	SKMC	muscle:	n/a
32	chr2:186603639-186603689	BE2_C	brain:	n/a
33	chr2:186603441-186603491	GM12878	blood:	n/a
34	chr2:186603639-186603689	ECC-1	luminal epithelium:	n/a
35	chr2:186603639-186603689	T-47D	breast:	n/a
36	chr2:186727863-186727913	HL-60	blood:	n/a
37	chr2:186609566-186609616	T-47D	breast:	n/a
38	chr2:186603398-186603448	NHDF-neo	bronchial:	n/a
39	chr2:186727863-186727913	GM06990	blood:	n/a
40	chr2:186603441-186603491	Caco-2	colon:	n/a
41	chr2:186603561-186603611	RPTEC	kidney:	n/a
42	chr2:186603398-186603448	HCF	heart:	n/a
43	chr2:186603981-186604031	ovcar-3	ovarian:	n/a
44	chr2:186603441-186603491	SAEC	small airway:	n/a
45	chr2:186601802-186601852	NHDF-neo	bronchial:	n/a
46	chr2:186603561-186603611	GM06990	blood:	n/a
47	chr2:186603441-186603491	PrEC	prostate:	n/a
48	chr2:186603398-186603448	HL-60	blood:	n/a
49	chr2:186609566-186609616	ovcar-3	ovarian:	n/a
50	chr2:186603981-186604031	AG10803	skin:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:186603293..186603807-chr8:145027949..145028449,2	MCF-7	breast:
2	chr2:186734702..186736953-chr2:186739550..186741965,2	MCF-7	breast:
3	chr2:186540633..186542551-chr2:186567883..186570534,2	MCF-7	breast:
4	chr2:186667156..186668174-chr2:186678025..186679009,3	MCF-7	breast:
5	chr2:186532536..186534671-chr2:186536499..186538385,2	K562	blood:
6	chr2:186597190..186601859-chr2:186602437..186604775,4	K562	blood:
7	chr2:186492938..186493701-chr2:186603922..186604721,2	MCF-7	breast:
8	chr2:186658483..186660924-chr2:186661633..186664592,2	MCF-7	breast:
9	chr2:186669335..186673195-chr2:186676461..186681487,4	MCF-7	breast:
10	chr2:186493563..186494107-chr2:187121512..187122407,2	MCF-7	breast:
11	chr2:186508722..186510476-chr2:186513123..186514706,2	K562	blood:
12	chr2:186668006..186669704-chr2:186673363..186675121,2	MCF-7	breast:
13	chr2:186741094..186742675-chr2:186744709..186747466,2	K562	blood:
14	chr2:186734702..186736953-chr2:186739550..186741965,2	MCF-7	breast:
15	chr2:186657715..186659336-chr2:186665984..186667594,2	K562	blood:
16	chr2:186717272..186719201-chr2:186720753..186722385,2	K562	blood:
17	chr2:186677322..186681085-chr2:186681928..186686220,4	MCF-7	breast:
18	chr2:186650871..186652540-chr2:186657235..186659322,2	K562	blood:
19	chr2:186650871..186652540-chr2:186657235..186659322,2	K562	blood:
20	chr2:186717400..186719050-chr2:186723710..186725689,2	K562	blood:
21	chr2:186614301..186616575-chr2:186619081..186620745,2	MCF-7	breast:
22	chr2:186741175..186743547-chr2:186745596..186747466,2	K562	blood:
23	chr2:186760390..186763157-chr2:186764375..186766387,2	K562	blood:
24	chr2:186720960..186722500-chr2:186726629..186729211,2	K562	blood:
25	chr2:186720960..186722500-chr2:186726629..186729211,2	K562	blood:
26	chr2:186778448..186780007-chr2:186782910..186785814,2	K562	blood:
27	chr2:186540633..186542551-chr2:186567883..186570534,2	MCF-7	breast:
28	chr2:186657715..186659336-chr2:186665984..186667594,2	K562	blood:
29	chr2:186717400..186719050-chr2:186723710..186725689,2	K562	blood:
30	chr2:186741094..186742675-chr2:186744709..186747466,2	K562	blood:
31	chr2:186603504..186604272-chr2:186667407..186668108,2	MCF-7	breast:
32	chr2:186807275..186808106-chr7:110453455..110454048,2	HCT-116	colon:
33	chr16:88876629..88878732-chr2:186490716..186492785,2	MCF-7	breast:
34	chr2:186778448..186780007-chr2:186782910..186785814,2	K562	blood:
35	chr2:186603383..186603935-chr8:145027949..145028449,2	MCF-7	breast:
36	chr2:186771348..186773239-chr22:46970196..46972979,2	MCF-7	breast:
37	chr2:186741175..186743547-chr2:186745596..186747466,2	K562	blood:
38	chr14:42041047..42041943-chr2:186615944..186616587,2	MCF-7	breast:
39	chr2:186508722..186510476-chr2:186513123..186514706,2	K562	blood:
40	chr2:186667156..186668174-chr2:186678025..186679009,3	MCF-7	breast:
41	chr2:186588408..186592015-chr2:186593924..186596626,4	K562	blood:
42	chr2:186594845..186596919-chr2:186599054..186601841,2	K562	blood:
43	chr2:186760390..186763157-chr2:186764375..186766387,2	K562	blood:
44	chr2:186676855..186679682-chr2:187312216..187314480,2	MCF-7	breast:
45	chr2:186598239..186601001-chr2:186602437..186604775,2	K562	blood:
46	chr2:186791324..186793332-chr2:186796322..186798371,2	K562	blood:
47	chr2:186669335..186673195-chr2:186676461..186681487,4	MCF-7	breast:
48	chr2:186493592..186494450-chr2:186603275..186603898,3	MCF-7	breast:
49	chr2:186608726..186611279-chr2:186612824..186614382,2	MCF-7	breast:
50	chr2:186717272..186719201-chr2:186720753..186722385,2	K562	blood:

(count:42 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-5	chr2:186652747-186652936	ENSG00000231646.1
2	lnc-ZSWIM2-6	chr2:186602913-186602980	ENSG00000226747
3	lnc-ZSWIM2-6	chr2:186603297-186603448	ENSG00000226747
4	lnc-ZSWIM2-6	chr2:186594056-186594164	ENSG00000226747
5	lnc-ZSWIM2-5	chr2:186653493-186653670	ENSG00000231646.1
6	lnc-ZSWIM2-6	chr2:186600789-186600864	NONHSAT075968
7	lnc-ZSWIM2-6	chr2:186600789-186600864	ENSG00000226747
8	lnc-ZSWIM2-6	chr2:186594056-186594164	ENSG00000226747
9	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110216
10	lnc-ZSWIM2-6	chr2:186594072-186594164	NONHSAT075968
11	lnc-ZSWIM2-4	chr2:186815194-186815488	XLOC_002427
12	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110214
13	lnc-ZSWIM2-14	chr2:186606631-186606774	l_2006_chr2:186606630-186611407_prostate
14	lnc-ZSWIM2-6	chr2:186584601-186585447	ENSG00000226747
15	lnc-ZSWIM2-6	chr2:186600789-186600930	NONHSAT075967
16	lnc-ZSWIM2-5	chr2:186664807-186664877	ENSG00000231646.1
17	lnc-ZSWIM2-14	chr2:186611303-186611407	l_2006_chr2:186606630-186611407_prostate
18	lnc-ZSWIM2-5	chr2:186653493-186653670	ENSG00000231646.1
19	lnc-ZSWIM2-6	chr2:186603634-186603808	NONHSAT075968
20	lnc-ZSWIM2-4	chr2:186817485-186817647	XLOC_002427
21	lnc-ZSWIM2-6	chr2:186605106-186605204	NR_110217
22	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110216
23	lnc-ZSWIM2-6	chr2:186594009-186594164	NONHSAT075967
24	lnc-ZSWIM2-6	chr2:186603634-186603820	NR_110214
25	lnc-ZSWIM2-5	chr2:186648418-186648857	ENSG00000231646.1
26	lnc-ZSWIM2-6	chr2:186605106-186605206	ENSG00000226747
27	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110217
28	lnc-ZSWIM2-6	chr2:186600789-186600859	NR_110215
29	lnc-ZSWIM2-6	chr2:186584939-186585447	ENSG00000226747
30	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110215
31	lnc-ZSWIM2-6	chr2:186600789-186600864	NR_110216
32	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110215
33	lnc-ZSWIM2-6	chr2:186603634-186603752	ENSG00000226747
34	lnc-ZSWIM2-6	chr2:186603297-186603446	NR_110215
35	lnc-ZSWIM2-6	chr2:186600789-186600864	NR_110214
36	lnc-ZSWIM2-5	chr2:186664807-186664878	ENSG00000231646.1
37	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110217
38	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110214
39	lnc-ZSWIM2-12	chr2:186800286-186800551	NONHSAT075977
40	lnc-ZSWIM2-13	chr2:186799635-186800049	NONHSAT075976
41	lnc-ZSWIM2-6	chr2:186603297-186603446	NR_110216
42	lnc-ZSWIM2-6	chr2:186600789-186600859	ENSG00000226747

No data

Variant related genes	Relation type
ENSG00000212581	TF binding region
FSIP2	TF binding region
ENSG00000226747	TF binding region
ENSG00000231646	TF binding region
ENSG00000212581	CpG island
FSIP2	CpG island
ENSG00000226747	CpG island
ENSG00000231646	CpG island
ENSG00000226747	chromatin interactions
ENSG00000075240	chromatin interactions
ENSG00000198931	chromatin interactions
ENSG00000188738	chromatin interactions
ENSG00000178209	chromatin interactions

Extended variants
information (count: 8299 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:8299 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180937857	chr2:186474076-186474077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566805047	chr2:186474078-186474079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534452547	chr2:186474124-186474125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572486610	chr2:186474237-186474238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544204883	chr2:186474241-186474242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs367912933	chr2:186474296-186474297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186033062	chr2:186474329-186474330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555674571	chr2:186474344-186474345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533567841	chr2:186474405-186474406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114249105	chr2:186474504-186474505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140320812	chr2:186474509-186474510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557018186	chr2:186474517-186474518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575346139	chr2:186474735-186474736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190227201	chr2:186474811-186474812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564419661	chr2:186474826-186474827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573164899	chr2:186474833-186474834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540429827	chr2:186474834-186474835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564114748	chr2:186474842-186474843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529407289	chr2:186474922-186474923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550765171	chr2:186474936-186474937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554962813	chr2:186475068-186475069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116449127	chr2:186475099-186475100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533185870	chr2:186475113-186475114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13013951	chr2:186475133-186475134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551360648	chr2:186475140-186475141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542950458	chr2:186475235-186475236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566866389	chr2:186475245-186475246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186026366	chr2:186475312-186475313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549558372	chr2:186475330-186475331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371800163	chr2:186475352-186475353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71430201	chr2:186475384-186475385	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557120332	chr2:186475393-186475394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146501000	chr2:186475452-186475453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115834632	chr2:186475571-186475572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2111710	chr2:186475590-186475591	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs149159932	chr2:186475605-186475606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565728293	chr2:186475633-186475634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540125048	chr2:186475665-186475666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561933244	chr2:186475708-186475709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573791119	chr2:186475744-186475745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72910219	chr2:186475762-186475763	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs556323010	chr2:186475774-186475775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533244762	chr2:186475784-186475785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375448967	chr2:186475788-186475789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13387585	chr2:186475794-186475795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13387594	chr2:186475828-186475829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148291120	chr2:186475840-186475841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528010531	chr2:186475867-186475868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549378028	chr2:186475870-186475871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369963906	chr2:186475888-186475889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
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
Urothelial carcinoma	21177765	CNVD
Ependymoma	20639864	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186473600-186483400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:186473800-186475000	Weak transcription	HMEC	breast
3	chr2:186475000-186475400	Enhancers	HMEC	breast
4	chr2:186475000-186476200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:186475800-186476000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:186483400-186483800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:186483400-186483800	Enhancers	Fetal Heart	heart
8	chr2:186483400-186484000	Enhancers	HMEC	breast
9	chr2:186483600-186483800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:186483600-186484000	Enhancers	NHEK	skin
11	chr2:186483800-186490400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:186485000-186485400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:186485400-186485800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:186485400-186490600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:186485800-186489800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:186487200-186487800	Enhancers	Brain Germinal Matrix	brain
17	chr2:186489800-186490400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:186490400-186490600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:186490600-186490800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:186498200-186498600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr2:186498200-186498800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr2:186498200-186498800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr2:186498400-186498800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr2:186498600-186503000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr2:186498800-186502400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr2:186498800-186503000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr2:186502400-186503800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr2:186502400-186504200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr2:186502600-186503200	Enhancers	Brain Germinal Matrix	brain
30	chr2:186502600-186503800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:186502800-186503400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr2:186502800-186503400	Enhancers	Fetal Brain Female	brain
33	chr2:186503000-186503400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr2:186503000-186503400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:186503000-186503800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:186503800-186508200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:186504200-186509000	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr2:186504800-186505400	Enhancers	Fetal Stomach	stomach
39	chr2:186505400-186508400	Weak transcription	Fetal Stomach	stomach
40	chr2:186507000-186507200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:186507000-186510400	Enhancers	Fetal Intestine Small	intestine
42	chr2:186507000-186511000	Enhancers	Fetal Intestine Large	intestine
43	chr2:186507200-186508400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:186507600-186511200	Enhancers	HepG2	liver
45	chr2:186508200-186509000	Enhancers	Ovary	ovary
46	chr2:186508200-186510000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:186508400-186509200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:186508400-186509200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:186508400-186509200	Enhancers	Fetal Stomach	stomach
50	chr2:186509000-186509600	Weak transcription	Ovary	ovary

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