Variant report

Variant	nsv584019
Chromosome Location	chr2:186445393-186866874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1878)
CpG islands
(count:549)
Chromatin interactive
region (count:66)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1878 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:186853506-186853842	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:186678380-186678904	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:186766781-186767039	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:186855637-186856004	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:186835223-186835544	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:186756102-186757040	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:186510210-186510829	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:186603689-186603907	HepG2	liver:	n/a	n/a
9	ATF1	chr2:186586784-186586978	K562	blood:	n/a	n/a
10	ATF1	chr2:186693024-186693115	K562	blood:	n/a	n/a
11	ATF2	chr2:186509544-186509954	GM12878	blood:	n/a	n/a
12	ATF2	chr2:186603605-186603967	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr2:186603621-186603950	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:186698786-186698866	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr2:186603273-186603956	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr2:186855743-186855846	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr2:186650918-186651197	GM12878	blood:	n/a	chr2:186651050-186651061
18	BATF	chr2:186650911-186651150	GM12878	blood:	n/a	chr2:186651050-186651061
19	BATF	chr2:186661618-186661923	GM12878	blood:	n/a	n/a
20	BATF	chr2:186509574-186509959	GM12878	blood:	n/a	n/a
21	BCLAF1	chr2:186509649-186509904	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:186678411-186678682	HepG2	liver:	n/a	n/a
23	BHLHE40	chr2:186727838-186727908	K562	blood:	n/a	n/a
24	BHLHE40	chr2:186678327-186678780	HepG2	liver:	n/a	n/a
25	BHLHE40	chr2:186591465-186591564	HepG2	liver:	n/a	n/a
26	BHLHE40	chr2:186678322-186678854	HepG2	liver:	n/a	n/a
27	BHLHE40	chr2:186603836-186603843	K562	blood:	n/a	n/a
28	BHLHE40	chr2:186603670-186603870	GM12878	blood:	n/a	n/a
29	BRCA1	chr2:186603628-186603971	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr2:186603755-186603918	HepG2	liver:	n/a	n/a
31	BRCA1	chr2:186775907-186775908	GM12878	blood:	n/a	n/a
32	CBX3	chr2:186447908-186448538	HCT-116	colon:	n/a	n/a
33	CBX3	chr2:186700648-186700857	K562	blood:	n/a	n/a
34	CBX3	chr2:186554740-186555339	HCT-116	colon:	n/a	n/a
35	CBX3	chr2:186836912-186837170	K562	blood:	n/a	n/a
36	CBX3	chr2:186447981-186448661	HCT-116	colon:	n/a	n/a
37	CBX3	chr2:186603562-186604004	K562	blood:	n/a	n/a
38	CBX3	chr2:186554778-186555281	HCT-116	colon:	n/a	n/a
39	CCNT2	chr2:186663343-186663462	K562	blood:	n/a	n/a
40	CCNT2	chr2:186798987-186799212	K562	blood:	n/a	n/a
41	CCNT2	chr2:186508599-186508741	K562	blood:	n/a	n/a
42	CCNT2	chr2:186603668-186603984	K562	blood:	n/a	n/a
43	CEBPB	chr2:186703330-186703591	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:186478620-186478884	HepG2	liver:	n/a	chr2:186478732-186478743
45	CEBPB	chr2:186533467-186533798	Hela-S3	cervix:	n/a	chr2:186533645-186533656
46	CEBPB	chr2:186719492-186720096	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr2:186863446-186863745	Hela-S3	cervix:	n/a	chr2:186863590-186863601
48	CEBPB	chr2:186448052-186448719	HCT-116	colon:	n/a	n/a
49	CEBPB	chr2:186686254-186686488	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:186722490-186722859	Hela-S3	cervix:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186603441-186603491	HCT-116	colon:	n/a
2	chr2:186603398-186603448	A549	lung:	n/a
3	chr2:186601802-186601852	HUVEC	blood vessel:	n/a
4	chr2:186603441-186603491	IMR90	lung:	fetal
5	chr2:186603398-186603448	U87	brain:	n/a
6	chr2:186603398-186603448	ovcar-3	ovarian:	n/a
7	chr2:186610279-186610329	HCPEpiC	choroid plexus:	n/a
8	chr2:186603981-186604031	IMR90	lung:	fetal
9	chr2:186609566-186609616	NB4	blood:	n/a
10	chr2:186727863-186727913	NHDF-neo	bronchial:	n/a
11	chr2:186727863-186727913	HRE	kidney:	n/a
12	chr2:186603639-186603689	K562	blood:	n/a
13	chr2:186603561-186603611	HIPEpiC	eye:	n/a
14	chr2:186603441-186603491	SAEC	small airway:	n/a
15	chr2:186603441-186603491	HUVEC	blood vessel:	n/a
16	chr2:186610279-186610329	HAEpiC	amniotic membrane:	n/a
17	chr2:186610279-186610329	AoSMC	blood vessel:	n/a
18	chr2:186727863-186727913	PrEC	prostate:	n/a
19	chr2:186603561-186603611	HEEpiC	esophagus:	n/a
20	chr2:186610279-186610329	SKMC	muscle:	n/a
21	chr2:186603441-186603491	NHBE	bronchial:	n/a
22	chr2:186610279-186610329	SK-N-SH_RA	brain:	n/a
23	chr2:186603441-186603491	NB4	blood:	n/a
24	chr2:186603441-186603491	Jurkat	blood:	n/a
25	chr2:186603398-186603448	HCT-116	colon:	n/a
26	chr2:186727863-186727913	HIPEpiC	eye:	n/a
27	chr2:186603561-186603611	BJ	skin:	n/a
28	chr2:186609566-186609616	HepG2	liver:	n/a
29	chr2:186603398-186603448	PFSK-1	brain:	n/a
30	chr2:186603981-186604031	AG10803	skin:	n/a
31	chr2:186727863-186727913	ovcar-3	ovarian:	n/a
32	chr2:186727863-186727913	Jurkat	blood:	n/a
33	chr2:186603398-186603448	AG10803	skin:	n/a
34	chr2:186603398-186603448	SKMC	muscle:	n/a
35	chr2:186601802-186601852	Caco-2	colon:	n/a
36	chr2:186609566-186609616	U87	brain:	n/a
37	chr2:186603981-186604031	GM12892	blood:	n/a
38	chr2:186601802-186601852	HEK293	kidney:	embryo
39	chr2:186610279-186610329	SK-N-MC	brain:	n/a
40	chr2:186603639-186603689	GM06990	blood:	n/a
41	chr2:186603639-186603689	NB4	blood:	n/a
42	chr2:186727863-186727913	Hepatocyte	liver:	n/a
43	chr2:186603639-186603689	HRE	kidney:	n/a
44	chr2:186603981-186604031	NHBE	bronchial:	n/a
45	chr2:186727863-186727913	AG04450	lung:	fetal
46	chr2:186603639-186603689	HEK293	kidney:	embryo
47	chr2:186609566-186609616	RPTEC	kidney:	n/a
48	chr2:186727863-186727913	GM12891	blood:	n/a
49	chr2:186727863-186727913	HMEC	breast:	n/a
50	chr2:186601802-186601852	CMK	blood:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:186717400..186719050-chr2:186723710..186725689,2	K562	blood:
2	chr2:186851763..186854059-chr2:186854208..186855953,2	MCF-7	breast:
3	chr2:186603293..186603807-chr8:145027949..145028449,2	MCF-7	breast:
4	chr2:186492938..186493701-chr2:186603922..186604721,2	MCF-7	breast:
5	chr2:186791324..186793332-chr2:186796322..186798371,2	K562	blood:
6	chr2:186532536..186534671-chr2:186536499..186538385,2	K562	blood:
7	chr2:186493563..186494107-chr2:187121512..187122407,2	MCF-7	breast:
8	chr2:186760390..186763157-chr2:186764375..186766387,2	K562	blood:
9	chr2:186493592..186494450-chr2:186603275..186603898,3	MCF-7	breast:
10	chr2:186598239..186601001-chr2:186602437..186604775,2	K562	blood:
11	chr2:186603504..186604272-chr2:186667407..186668108,2	MCF-7	breast:
12	chr2:186677322..186681085-chr2:186681928..186686220,4	MCF-7	breast:
13	chr2:186717272..186719201-chr2:186720753..186722385,2	K562	blood:
14	chr2:186614301..186616575-chr2:186619081..186620745,2	MCF-7	breast:
15	chr2:186540633..186542551-chr2:186567883..186570534,2	MCF-7	breast:
16	chr2:186473268..186473794-chr2:186603435..186603983,2	MCF-7	breast:
17	chr2:186597190..186601859-chr2:186602437..186604775,4	K562	blood:
18	chr2:186720960..186722500-chr2:186726629..186729211,2	K562	blood:
19	chr2:186608726..186611279-chr2:186612824..186614382,2	MCF-7	breast:
20	chr2:186861297..186864828-chr2:186866334..186869154,3	K562	blood:
21	chr17:57913762..57915412-chr2:186861621..186864023,2	MCF-7	breast:
22	chr2:186778448..186780007-chr2:186782910..186785814,2	K562	blood:
23	chr2:186508722..186510476-chr2:186513123..186514706,2	K562	blood:
24	chr2:186667156..186668174-chr2:186678025..186679009,3	MCF-7	breast:
25	chr2:186594845..186596919-chr2:186599054..186601841,2	K562	blood:
26	chr2:186658483..186660924-chr2:186661633..186664592,2	MCF-7	breast:
27	chr2:186760390..186763157-chr2:186764375..186766387,2	K562	blood:
28	chr2:186657715..186659336-chr2:186665984..186667594,2	K562	blood:
29	chr2:186720960..186722500-chr2:186726629..186729211,2	K562	blood:
30	chr2:186588408..186592015-chr2:186593924..186596626,4	K562	blood:
31	chr2:186861297..186864828-chr2:186866334..186869154,3	K562	blood:
32	chr2:186669335..186673195-chr2:186676461..186681487,4	MCF-7	breast:
33	chr2:186508722..186510476-chr2:186513123..186514706,2	K562	blood:
34	chr2:186844422..186846233-chr2:187042627..187045441,2	K562	blood:
35	chr2:186603383..186603935-chr8:145027949..145028449,2	MCF-7	breast:
36	chr2:186540633..186542551-chr2:186567883..186570534,2	MCF-7	breast:
37	chr2:186650871..186652540-chr2:186657235..186659322,2	K562	blood:
38	chr2:186715733..186716239-chr20:13748197..13748697,2	MCF-7	breast:
39	chr2:186668006..186669704-chr2:186673363..186675121,2	MCF-7	breast:
40	chr2:186650871..186652540-chr2:186657235..186659322,2	K562	blood:
41	chr2:186594845..186596919-chr2:186599054..186601841,2	K562	blood:
42	chr2:186741094..186742675-chr2:186744709..186747466,2	K562	blood:
43	chr2:186677322..186681085-chr2:186681928..186686220,4	MCF-7	breast:
44	chr16:88876629..88878732-chr2:186490716..186492785,2	MCF-7	breast:
45	chr2:186588408..186592015-chr2:186593924..186596626,4	K562	blood:
46	chr2:186669335..186673195-chr2:186676461..186681487,4	MCF-7	breast:
47	chr2:186657715..186659336-chr2:186665984..186667594,2	K562	blood:
48	chr2:186667156..186668174-chr2:186678025..186679009,3	MCF-7	breast:
49	chr2:186532536..186534671-chr2:186536499..186538385,2	K562	blood:
50	chr2:186851763..186854059-chr2:186854208..186855953,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110214
2	lnc-ZSWIM2-14	chr2:186606631-186606774	l_2006_chr2:186606630-186611407_prostate
3	lnc-ZSWIM2-5	chr2:186664807-186664877	ENSG00000231646.1
4	lnc-ZSWIM2-5	chr2:186652747-186652936	ENSG00000231646.1
5	lnc-ZSWIM2-5	chr2:186648418-186648857	ENSG00000231646.1
6	lnc-ZSWIM2-5	chr2:186653493-186653670	ENSG00000231646.1
7	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110216
8	lnc-ZSWIM2-5	chr2:186653493-186653670	ENSG00000231646.1
9	lnc-ZSWIM2-14	chr2:186611303-186611407	l_2006_chr2:186606630-186611407_prostate
10	lnc-ZSWIM2-6	chr2:186603297-186603446	NR_110215
11	lnc-ZSWIM2-6	chr2:186603634-186603752	ENSG00000226747
12	lnc-ZSWIM2-6	chr2:186602913-186602980	ENSG00000226747
13	lnc-ZSWIM2-6	chr2:186600789-186600859	ENSG00000226747
14	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110217
15	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110214
16	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110215
17	lnc-ZSWIM2-6	chr2:186600789-186600864	NR_110216
18	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110216
19	lnc-ZSWIM2-4	chr2:186817485-186817647	XLOC_002427
20	lnc-ZSWIM2-6	chr2:186594056-186594164	ENSG00000226747
21	lnc-ZSWIM2-13	chr2:186799635-186800049	NONHSAT075976
22	lnc-ZSWIM2-6	chr2:186605106-186605206	ENSG00000226747
23	lnc-ZSWIM2-6	chr2:186603634-186603820	NR_110214
24	lnc-ZSWIM2-6	chr2:186584939-186585447	ENSG00000226747
25	lnc-ZSWIM2-4	chr2:186815194-186815488	XLOC_002427
26	lnc-ZSWIM2-6	chr2:186600789-186600859	NR_110215
27	lnc-ZSWIM2-6	chr2:186594009-186594164	NONHSAT075967
28	lnc-ZSWIM2-6	chr2:186603634-186603808	NONHSAT075968
29	lnc-ZSWIM2-6	chr2:186600789-186600864	NR_110214
30	lnc-ZSWIM2-6	chr2:186605106-186605204	NR_110217
31	lnc-ZSWIM2-6	chr2:186594072-186594164	NONHSAT075968
32	lnc-ZSWIM2-6	chr2:186603297-186603448	ENSG00000226747
33	lnc-ZSWIM2-6	chr2:186600789-186600864	NONHSAT075968
34	lnc-ZSWIM2-6	chr2:186600789-186600930	NONHSAT075967
35	lnc-ZSWIM2-6	chr2:186584601-186585447	ENSG00000226747
36	lnc-ZSWIM2-12	chr2:186800286-186800551	NONHSAT075977
37	lnc-ZSWIM2-11	chr2:186821314-186821790	NONHSAT075979
38	lnc-ZSWIM2-6	chr2:186594056-186594164	NR_110217
39	lnc-ZSWIM2-5	chr2:186664807-186664878	ENSG00000231646.1
40	lnc-ZSWIM2-6	chr2:186584601-186585447	NR_110215
41	lnc-ZSWIM2-6	chr2:186600789-186600864	ENSG00000226747
42	lnc-ZSWIM2-6	chr2:186603297-186603446	NR_110216
43	lnc-ZSWIM2-6	chr2:186594056-186594164	ENSG00000226747

No data

Variant related genes	Relation type
RPL21P32	TF binding region
ENSG00000212581	TF binding region
ENSG00000231646	TF binding region
FSIP2	TF binding region
ENSG00000226747	TF binding region
RPL21P32	CpG island
ENSG00000212581	CpG island
ENSG00000231646	CpG island
FSIP2	CpG island
ENSG00000226747	CpG island
ENSG00000062716	chromatin interactions
ENSG00000188738	chromatin interactions
ENSG00000178209	chromatin interactions
ENSG00000226747	chromatin interactions
ENSG00000198931	chromatin interactions
ENSG00000075240	chromatin interactions

Extended variants
information (count: 11120 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:11120 , 50 per page) page: 1 2 3 4 5 6 7 ... 223

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7604780	chr2:186445393-186445394	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375634211	chr2:186445419-186445420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147989034	chr2:186445426-186445427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs66508949	chr2:186445438-186445439	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs531779263	chr2:186445462-186445463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374450895	chr2:186445490-186445491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562400299	chr2:186445491-186445492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532954889	chr2:186445522-186445523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368818085	chr2:186445531-186445532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566450691	chr2:186445539-186445540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527617092	chr2:186445621-186445622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565591663	chr2:186445648-186445649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549262666	chr2:186445653-186445654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567474440	chr2:186445670-186445671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201401733	chr2:186445706-186445707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368182842	chr2:186445737-186445738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547052557	chr2:186445738-186445739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529421188	chr2:186445741-186445742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112718215	chr2:186445795-186445796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572155158	chr2:186445804-186445805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557633383	chr2:186445805-186445806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542905089	chr2:186445831-186445832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561280928	chr2:186445843-186445844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147223454	chr2:186445942-186445943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375880412	chr2:186445961-186445962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538743770	chr2:186446015-186446016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs137937495	chr2:186446028-186446029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72906168	chr2:186446037-186446038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537321926	chr2:186446040-186446041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375597262	chr2:186446056-186446057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189067589	chr2:186446086-186446087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555746515	chr2:186446087-186446088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542929944	chr2:186446088-186446089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140478306	chr2:186446143-186446144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371950371	chr2:186446145-186446146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543613175	chr2:186446273-186446274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565468621	chr2:186446277-186446278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77777227	chr2:186446293-186446294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182572053	chr2:186446357-186446358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs13021527	chr2:186446390-186446391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187217932	chr2:186446467-186446468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560203648	chr2:186446482-186446483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527248282	chr2:186446486-186446487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541397762	chr2:186446532-186446533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549261876	chr2:186446548-186446549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79476841	chr2:186446567-186446568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190452473	chr2:186446774-186446775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs180954911	chr2:186446822-186446823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184946532	chr2:186446910-186446911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538782874	chr2:186446949-186446950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Pancreatic cancer	17952125	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:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186433000-186447400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:186436000-186452200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:186444400-186447400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:186444400-186447600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:186444400-186447600	Weak transcription	Stomach Mucosa	stomach
6	chr2:186446200-186446600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:186446400-186449600	Enhancers	HMEC	breast
8	chr2:186446400-186451600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr2:186446600-186448400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:186446800-186447400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:186447400-186448800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
12	chr2:186447400-186448800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:186447400-186448800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr2:186447400-186448800	Enhancers	NHEK	skin
15	chr2:186447400-186449000	Enhancers	Hela-S3	cervix
16	chr2:186447600-186447800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:186447600-186448200	Enhancers	Stomach Mucosa	stomach
18	chr2:186447600-186448600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
19	chr2:186447600-186449000	Enhancers	HSMM	muscle
20	chr2:186447800-186448200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:186447800-186448200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr2:186447800-186448600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:186447800-186449200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:186448000-186448600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr2:186448200-186448600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:186448200-186449000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr2:186448800-186449200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:186449200-186450000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:186450000-186467200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:186455800-186456600	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr2:186455800-186456600	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr2:186456200-186457200	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr2:186463000-186463600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr2:186463000-186464000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:186463200-186463400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:186463200-186463800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr2:186463200-186464000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:186463200-186464200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr2:186463200-186464200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr2:186464000-186464200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:186467200-186468000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr2:186468000-186473000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr2:186473000-186473600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr2:186473000-186473800	Enhancers	HMEC	breast
45	chr2:186473400-186473800	Enhancers	Fetal Kidney	kidney
46	chr2:186473600-186483400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:186473800-186475000	Weak transcription	HMEC	breast
48	chr2:186475000-186475400	Enhancers	HMEC	breast
49	chr2:186475000-186476200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr2:186475800-186476000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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