Variant report

Variant	nsv582273
Chromosome Location	chr2:78432494-78978011
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1665)
CpG islands
(count:244)
Chromatin interactive
region (count:76)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1665 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:78653375-78653864	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:78769269-78769309	K562	blood:	n/a	n/a
3	ARID3A	chr2:78532952-78532953	K562	blood:	n/a	n/a
4	ARID3A	chr2:78578413-78578720	K562	blood:	n/a	n/a
5	ARID3A	chr2:78767880-78769546	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:78773878-78773884	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:78758882-78759153	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:78578391-78578636	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:78767306-78767748	K562	blood:	n/a	n/a
10	ARID3A	chr2:78762637-78762893	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:78643666-78644757	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:78487915-78488675	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:78900306-78900320	K562	blood:	n/a	n/a
14	ATF1	chr2:78768965-78769410	K562	blood:	n/a	n/a
15	ATF2	chr2:78900116-78900488	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr2:78900244-78900408	K562	blood:	n/a	n/a
17	ATF3	chr2:78768931-78769163	K562	blood:	n/a	n/a
18	BACH1	chr2:78768931-78769174	K562	blood:	n/a	n/a
19	BACH1	chr2:78760235-78760522	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr2:78477710-78477711	K562	blood:	n/a	n/a
21	BATF	chr2:78508306-78508624	GM12878	blood:	n/a	n/a
22	BATF	chr2:78508305-78508535	GM12878	blood:	n/a	n/a
23	BATF	chr2:78928653-78928861	GM12878	blood:	n/a	n/a
24	BATF	chr2:78928654-78928933	GM12878	blood:	n/a	n/a
25	BCL11A	chr2:78508311-78508495	GM12878	blood:	n/a	n/a
26	BCL11A	chr2:78928660-78928905	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:78928643-78928874	GM12878	blood:	n/a	n/a
28	BHLHE40	chr2:78487986-78488343	HepG2	liver:	n/a	n/a
29	BHLHE40	chr2:78900370-78900478	GM12878	blood:	n/a	n/a
30	BHLHE40	chr2:78508455-78508636	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:78768960-78769172	K562	blood:	n/a	n/a
32	BHLHE40	chr2:78490807-78490864	GM12878	blood:	n/a	n/a
33	BRCA1	chr2:78768882-78769066	HepG2	liver:	n/a	n/a
34	BRCA1	chr2:78872040-78872087	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr2:78768872-78769471	K562	blood:	n/a	n/a
36	CBX3	chr2:78768994-78769438	K562	blood:	n/a	n/a
37	CCNT2	chr2:78928938-78929138	K562	blood:	n/a	n/a
38	CCNT2	chr2:78768803-78769195	K562	blood:	n/a	n/a
39	CEBPB	chr2:78518565-78518897	HepG2	liver:	n/a	chr2:78518707-78518718
40	CEBPB	chr2:78948457-78948823	IMR90	lung:	n/a	chr2:78948637-78948646 chr2:78948733-78948744 chr2:78948733-78948744 chr2:78948635-78948648 chr2:78948462-78948473 chr2:78948637-78948646 chr2:78948637-78948646 chr2:78948733-78948746
41	CEBPB	chr2:78537183-78537401	K562	blood:	n/a	n/a
42	CEBPB	chr2:78780127-78780642	A549	lung:	n/a	chr2:78780516-78780527
43	CEBPB	chr2:78489042-78489325	HepG2	liver:	n/a	chr2:78489173-78489184
44	CEBPB	chr2:78577077-78577375	IMR90	lung:	n/a	chr2:78577256-78577265 chr2:78577254-78577265 chr2:78577256-78577267 chr2:78577256-78577265 chr2:78577256-78577265 chr2:78577256-78577265
45	CEBPB	chr2:78641631-78642288	IMR90	lung:	n/a	chr2:78641752-78641763
46	CEBPB	chr2:78858310-78858571	K562	blood:	n/a	chr2:78858413-78858424
47	CEBPB	chr2:78904048-78904415	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:78948458-78948809	A549	lung:	n/a	chr2:78948637-78948646 chr2:78948733-78948744 chr2:78948733-78948744 chr2:78948635-78948648 chr2:78948462-78948473 chr2:78948637-78948646 chr2:78948637-78948646 chr2:78948733-78948746
49	CEBPB	chr2:78749998-78750373	HepG2	liver:	n/a	chr2:78750179-78750192 chr2:78750181-78750190
50	CEBPB	chr2:78445231-78445483	H1-hESC	embryonic stem cell:	n/a	chr2:78445380-78445391

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:78769016-78769066	SK-N-SH_RA	brain:	n/a
2	chr2:78768994-78769044	MCF10A-Er-Src	breast:	n/a
3	chr2:78768994-78769044	GM06990	blood:	n/a
4	chr2:78928852-78928902	HUVEC	blood vessel:	n/a
5	chr2:78928852-78928902	MCF10A-Er-Src	breast:	n/a
6	chr2:78769016-78769066	PrEC	prostate:	n/a
7	chr2:78768994-78769044	ProgFib	skin:	n/a
8	chr2:78928852-78928902	BE2_C	brain:	n/a
9	chr2:78928852-78928902	LNCaP	prostate:	n/a
10	chr2:78928852-78928902	H1-hESC	embryonic stem cell:	embryo
11	chr2:78768994-78769044	NHBE	bronchial:	n/a
12	chr2:78928852-78928902	T-47D	breast:	n/a
13	chr2:78928852-78928902	NHDF-neo	bronchial:	n/a
14	chr2:78769016-78769066	HIPEpiC	eye:	n/a
15	chr2:78928852-78928902	HAEpiC	amniotic membrane:	n/a
16	chr2:78768994-78769044	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:78545567-78545617	AG09309	skin:	n/a
18	chr2:78769016-78769066	MCF10A-Er-Src	breast:	n/a
19	chr2:78928852-78928902	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:78768994-78769044	HRPEpiC	eye:	n/a
21	chr2:78768994-78769044	HAEpiC	amniotic membrane:	n/a
22	chr2:78545567-78545617	PANC-1	pancreas:	n/a
23	chr2:78545567-78545617	ECC-1	luminal epithelium:	n/a
24	chr2:78769016-78769066	HL-60	blood:	n/a
25	chr2:78768994-78769044	HRCEpiC	kidney:	n/a
26	chr2:78928852-78928902	A549	lung:	n/a
27	chr2:78545567-78545617	HIPEpiC	eye:	n/a
28	chr2:78928852-78928902	K562	blood:	n/a
29	chr2:78768994-78769044	H1-hESC	embryonic stem cell:	embryo
30	chr2:78769016-78769066	GM12878	blood:	n/a
31	chr2:78545567-78545617	NH-A	brain:	n/a
32	chr2:78545567-78545617	A549	lung:	n/a
33	chr2:78768994-78769044	A549	lung:	n/a
34	chr2:78769016-78769066	HCPEpiC	choroid plexus:	n/a
35	chr2:78768994-78769044	AG09319	gingival:	n/a
36	chr2:78928852-78928902	HEK293	kidney:	embryo
37	chr2:78928852-78928902	Hela-S3	cervix:	n/a
38	chr2:78768994-78769044	HCPEpiC	choroid plexus:	n/a
39	chr2:78928852-78928902	HEEpiC	esophagus:	n/a
40	chr2:78768994-78769044	IMR90	lung:	fetal
41	chr2:78769016-78769066	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:78928852-78928902	AG09309	skin:	n/a
43	chr2:78769016-78769066	NT2-D1	testis:	n/a
44	chr2:78928852-78928902	NB4	blood:	n/a
45	chr2:78769016-78769066	ProgFib	skin:	n/a
46	chr2:78928852-78928902	AG09319	gingival:	n/a
47	chr2:78545567-78545617	AG04450	lung:	fetal
48	chr2:78769016-78769066	SK-N-SH	brain:	n/a
49	chr2:78769016-78769066	BE2_C	brain:	n/a
50	chr2:78928852-78928902	AoSMC	blood vessel:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:78753644..78755915-chr2:78762930..78764798,2	K562	blood:
2	chr2:78805460..78806996-chr2:78842740..78844663,2	K562	blood:
3	chr2:78637554..78639977-chr2:78766787..78768860,2	K562	blood:
4	chr2:78658404..78659062-chr2:79206498..79207224,3	MCF-7	breast:
5	chr2:78760713..78763886-chr2:78766006..78769531,4	K562	blood:
6	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
7	chr2:78577613..78578539-chr2:79206466..79207847,3	MCF-7	breast:
8	chr2:78747682..78749204-chr2:78751235..78753165,2	K562	blood:
9	chr2:78760713..78763886-chr2:78766006..78769531,4	K562	blood:
10	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
11	chr2:78763390..78765848-chr2:78770837..78772654,2	K562	blood:
12	chr2:78687302..78689394-chr2:78702872..78704887,2	K562	blood:
13	chr2:78753315..78756204-chr2:78756434..78759227,3	K562	blood:
14	chr2:78753644..78755915-chr2:78762930..78764798,2	K562	blood:
15	chr2:78748455..78750783-chr2:78766208..78769872,3	K562	blood:
16	chr2:78754724..78757697-chr2:78759967..78762678,2	K562	blood:
17	chr2:78815181..78817318-chr2:78826193..78827770,2	K562	blood:
18	chr2:78716026..78716644-chr5:124520515..124521066,2	MCF-7	breast:
19	chr2:78757746..78759593-chr2:78760863..78763022,2	K562	blood:
20	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
21	chr2:78957735..78959501-chr2:78965066..78967357,2	K562	blood:
22	chr2:78936980..78938756-chr2:78942591..78944856,2	K562	blood:
23	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
24	chr2:78828832..78831056-chr2:78839903..78841751,2	K562	blood:
25	chr2:78577011..78577791-chr8:96157456..96158424,2	MCF-7	breast:
26	chr2:78715619..78718403-chr2:78734378..78736993,2	K562	blood:
27	chr2:78748455..78750783-chr2:78766208..78769872,3	K562	blood:
28	chr2:78519747..78522682-chr2:78785137..78786876,2	K562	blood:
29	chr2:78801958..78804161-chr2:78807594..78809953,2	K562	blood:
30	chr2:78695424..78698348-chr2:78698438..78701119,2	K562	blood:
31	chr1:91853012..91853572-chr2:78928953..78929458,2	MCF-7	breast:
32	chr2:78764342..78767175-chr2:78767388..78769753,3	K562	blood:
33	chr2:78749283..78751187-chr2:78766195..78769118,2	K562	blood:
34	chr2:78658362..78658925-chr2:79089675..79090181,2	MCF-7	breast:
35	chr2:78696080..78698215-chr2:78700355..78703022,2	K562	blood:
36	chr2:78687302..78689394-chr2:78702872..78704887,2	K562	blood:
37	chr2:78754724..78757697-chr2:78759967..78762678,2	K562	blood:
38	chr2:78815181..78817318-chr2:78826193..78827770,2	K562	blood:
39	chr2:78607954..78609567-chr2:78764622..78766807,2	K562	blood:
40	chr2:78709311..78711382-chr2:78715661..78717389,2	K562	blood:
41	chr2:78801958..78804161-chr2:78807594..78809953,2	K562	blood:
42	chr2:78828832..78831056-chr2:78839903..78841751,2	K562	blood:
43	chr2:78715619..78718403-chr2:78734378..78736993,2	K562	blood:
44	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
45	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
46	chr2:78637554..78639977-chr2:78766787..78768860,2	K562	blood:
47	chr2:78757746..78759593-chr2:78760863..78763022,2	K562	blood:
48	chr2:78696080..78698215-chr2:78700355..78703022,2	K562	blood:
49	chr2:78767623..78771004-chr2:78771071..78774505,4	K562	blood:
50	chr2:78758175..78760513-chr2:78766795..78770172,4	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRTM4-3	chr2:78768698-78769292	NONHSAT071835
2	lnc-REG3G-6	chr2:78913797-78913805	NONHSAT071853
3	lnc-REG1B-7	chr2:78678545-78678570	NONHSAT071849
4	lnc-LRRTM4-3	chr2:78714968-78715058	NONHSAT071835
5	lnc-REG3G-1	chr2:78825037-78825069	ENSG00000234877
6	lnc-LRRTM4-3	chr2:78768698-78769187	NONHSAT071846
7	lnc-REG1B-4	chr2:78825037-78825062	XLOC_002175
8	lnc-REG3G-6	chr2:78918402-78918413	NONHSAT071853
9	lnc-REG3G-1	chr2:78826195-78826532	ENSG00000234877
10	lnc-REG1B-7	chr2:78679696-78680040	NONHSAT071849
11	lnc-LRRTM4-3	chr2:78639673-78640302	NONHSAT071846
12	lnc-REG3G-6	chr2:78928684-78929025	NONHSAT071853
13	lnc-LRRTM4-3	chr2:78637204-78640302	NONHSAT071835
14	lnc-REG1B-4	chr2:78826188-78826532	XLOC_002175
15	lnc-LRRTM4-3	chr2:78712920-78712978	NONHSAT071835
16	lnc-LRRTM4-3	chr2:78639919-78640220	NONHSAT071847
17	lnc-LRRTM4-3	chr2:78683574-78683857	NONHSAT071835
18	lnc-REG3G-7	chr2:78664976-78666047	NONHSAT071848
19	lnc-LRRTM4-3	chr2:78517514-78517857	NR_110288
20	lnc-LRRTM4-3	chr2:78712920-78712978	NONHSAT071846

No data

Variant related genes	Relation type
CYCSP6	TF binding region
ENSG00000234877	TF binding region
ENSG00000270470	TF binding region
CYCSP6	CpG island
ENSG00000234877	CpG island
ENSG00000270470	CpG island
ENSG00000071553	chromatin interactions

Extended variants
information (count: 9826 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:9826 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183740327	chr2:78445405-78445406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543666209	chr2:78445420-78445421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114977566	chr2:78445424-78445425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188264047	chr2:78445441-78445442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534636725	chr2:78445532-78445533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547906390	chr2:78445585-78445586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561764978	chr2:78445607-78445608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568329567	chr2:78445617-78445618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536986065	chr2:78445619-78445620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557193626	chr2:78445625-78445626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370069938	chr2:78445675-78445676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150017720	chr2:78445676-78445677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145247736	chr2:78445677-78445678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192309161	chr2:78445704-78445705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148728495	chr2:78445748-78445749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111299019	chr2:78445842-78445843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555515365	chr2:78445869-78445870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575890542	chr2:78445915-78445916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143602835	chr2:78445937-78445938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78127426	chr2:78445940-78445941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs72927702	chr2:78445953-78445954	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs573767961	chr2:78445979-78445980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545466703	chr2:78445980-78445981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559379151	chr2:78446008-78446009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541212224	chr2:78446015-78446016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34900368	chr2:78446036-78446037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72929605	chr2:78446067-78446068	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs568012988	chr2:78446173-78446174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561654204	chr2:78447424-78447425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575443710	chr2:78447442-78447443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552322934	chr2:78447461-78447462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547180425	chr2:78447478-78447479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571040247	chr2:78447480-78447481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544216234	chr2:78447591-78447592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564115196	chr2:78447600-78447601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77131898	chr2:78447603-78447604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546587472	chr2:78447626-78447627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371480156	chr2:78447650-78447651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529098845	chr2:78447721-78447722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146936051	chr2:78447736-78447737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568996263	chr2:78447751-78447752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537990200	chr2:78447755-78447756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551358713	chr2:78447770-78447771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114376441	chr2:78447774-78447775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534467526	chr2:78447794-78447795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34915365	chr2:78447796-78447797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs137869302	chr2:78447813-78447814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574151354	chr2:78447820-78447821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536426093	chr2:78447971-78447972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556754560	chr2:78448001-78448002	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78445400-78445800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr2:78445600-78446200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:78445800-78446200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:78447400-78448200	Enhancers	Brain Hippocampus Middle	brain
5	chr2:78447600-78448400	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr2:78448200-78453200	Weak transcription	Brain Hippocampus Middle	brain
7	chr2:78448400-78448800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr2:78448800-78449400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr2:78453200-78454000	ZNF genes & repeats	Brain Hippocampus Middle	brain
10	chr2:78454000-78454400	Weak transcription	Brain Hippocampus Middle	brain
11	chr2:78459800-78472400	Weak transcription	HepG2	liver
12	chr2:78460800-78462000	Enhancers	Brain Substantia Nigra	brain
13	chr2:78467000-78467200	Enhancers	Brain Hippocampus Middle	brain
14	chr2:78467000-78468000	Weak transcription	Brain Substantia Nigra	brain
15	chr2:78467200-78468600	Weak transcription	Brain Hippocampus Middle	brain
16	chr2:78467200-78469000	Enhancers	Brain Cingulate Gyrus	brain
17	chr2:78468000-78469200	Enhancers	Brain Substantia Nigra	brain
18	chr2:78468600-78469000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr2:78468600-78469000	Enhancers	Brain Hippocampus Middle	brain
20	chr2:78469000-78472800	Weak transcription	Brain Hippocampus Middle	brain
21	chr2:78472400-78473200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:78472400-78473200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr2:78472400-78473400	Enhancers	HepG2	liver
24	chr2:78472600-78473000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:78472800-78473200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr2:78472800-78473200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:78472800-78473200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr2:78472800-78473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr2:78472800-78473200	ZNF genes & repeats	Brain Hippocampus Middle	brain
30	chr2:78472800-78473600	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr2:78473000-78473400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr2:78478200-78479000	Weak transcription	Brain Substantia Nigra	brain
33	chr2:78479000-78479200	ZNF genes & repeats	Brain Substantia Nigra	brain
34	chr2:78479200-78479400	Weak transcription	Brain Substantia Nigra	brain
35	chr2:78485800-78486000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:78485800-78486000	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr2:78486400-78487600	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr2:78487000-78488200	Enhancers	HepG2	liver
39	chr2:78487200-78489000	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:78487400-78489000	Enhancers	Brain Hippocampus Middle	brain
41	chr2:78487600-78488800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr2:78487600-78491600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:78487800-78488800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr2:78488000-78488200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:78488000-78489000	Enhancers	Brain Substantia Nigra	brain
46	chr2:78488200-78488600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:78488200-78489000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr2:78488200-78489600	Flanking Active TSS	HepG2	liver
49	chr2:78488400-78488800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:78488400-78488800	Enhancers	HUES6 Cell Line	embryonic stem cell

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