Variant report

Variant	esv3367963
Chromosome Location	chr4:85911017-86246036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1675)
CpG islands
(count:244)
Chromatin interactive
region (count:44)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1675 , 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	chr4:86229331-86229442	K562	blood:	n/a	n/a
2	ARID3A	chr4:85972764-85973132	HepG2	liver:	n/a	n/a
3	ATF2	chr4:86068585-86068976	GM12878	blood:	n/a	n/a
4	ATF3	chr4:86048845-86049075	K562	blood:	n/a	n/a
5	ATF3	chr4:86048684-86049181	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr4:86048748-86049111	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:86117223-86117513	K562	blood:	n/a	n/a
8	BACH1	chr4:86117184-86117484	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:86048880-86049071	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:86191038-86191060	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:86063742-86063931	GM12878	blood:	n/a	n/a
12	BATF	chr4:86063739-86064004	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:86048848-86049072	K562	blood:	n/a	n/a
14	BHLHE40	chr4:86068628-86068932	HepG2	liver:	n/a	n/a
15	BHLHE40	chr4:86005640-86005903	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:86068614-86068984	K562	blood:	n/a	n/a
17	BHLHE40	chr4:86068600-86068994	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:85927120-85927341	K562	blood:	n/a	n/a
19	BHLHE40	chr4:86048861-86049039	HepG2	liver:	n/a	n/a
20	BHLHE40	chr4:85927970-85928029	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:86004404-86004575	GM12878	blood:	n/a	n/a
22	BRCA1	chr4:86192905-86192925	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr4:86135175-86135202	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr4:85954983-85955371	K562	blood:	n/a	n/a
25	CBX3	chr4:86130228-86130740	HCT-116	colon:	n/a	chr4:86130519-86130530
26	CBX3	chr4:85955014-85955314	K562	blood:	n/a	n/a
27	CBX3	chr4:86048746-86049249	HCT-116	colon:	n/a	n/a
28	CBX3	chr4:86117241-86117526	K562	blood:	n/a	n/a
29	CBX3	chr4:86048765-86049237	HCT-116	colon:	n/a	n/a
30	CBX3	chr4:86048769-86049126	K562	blood:	n/a	n/a
31	CCNT2	chr4:86239533-86239580	K562	blood:	n/a	n/a
32	CEBPB	chr4:86120067-86120352	HepG2	liver:	n/a	chr4:86120180-86120191
33	CEBPB	chr4:85993762-85994070	HepG2	liver:	n/a	chr4:85993904-85993917 chr4:85993906-85993915 chr4:85993904-85993917 chr4:85993905-85993916 chr4:85993906-85993915 chr4:85993906-85993915 chr4:85993906-85993915
34	CEBPB	chr4:85927061-85927449	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:85957342-85957570	HepG2	liver:	n/a	chr4:85957488-85957499 chr4:85957486-85957499 chr4:85957486-85957497
36	CEBPB	chr4:86089702-86089927	H1-hESC	embryonic stem cell:	n/a	chr4:86089783-86089796 chr4:86089784-86089795
37	CEBPB	chr4:85950394-85950528	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:85986219-85986465	Hela-S3	cervix:	n/a	chr4:85986338-85986349 chr4:85986374-85986385
39	CEBPB	chr4:86089605-86089943	HepG2	liver:	n/a	chr4:86089783-86089796 chr4:86089784-86089795
40	CEBPB	chr4:85960440-85961170	HCT-116	colon:	n/a	chr4:85960789-85960800
41	CEBPB	chr4:85986196-85986548	HepG2	liver:	n/a	chr4:85986338-85986349 chr4:85986374-85986385
42	CEBPB	chr4:86169784-86170064	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:85935648-85935848	HepG2	liver:	n/a	chr4:85935701-85935718
44	CEBPB	chr4:86131439-86132112	HCT-116	colon:	n/a	n/a
45	CEBPB	chr4:85957393-85957601	IMR90	lung:	n/a	chr4:85957488-85957499 chr4:85957486-85957499 chr4:85957486-85957497
46	CEBPB	chr4:85971950-85972242	A549	lung:	n/a	chr4:85972093-85972104 chr4:85972091-85972102 chr4:85972091-85972104 chr4:85972047-85972058 chr4:85972093-85972102
47	CEBPB	chr4:86130183-86130797	HCT-116	colon:	n/a	chr4:86130529-86130542
48	CEBPB	chr4:86130281-86130786	A549	lung:	n/a	chr4:86130529-86130542
49	CEBPB	chr4:85986190-85986496	IMR90	lung:	n/a	chr4:85986338-85986349 chr4:85986374-85986385
50	CEBPB	chr4:85960636-85960966	A549	lung:	n/a	chr4:85960789-85960800

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:86167398-86167448	H1-hESC	embryonic stem cell:	embryo
2	chr4:86049133-86049183	AG10803	skin:	n/a
3	chr4:86224551-86224601	SK-N-MC	brain:	n/a
4	chr4:86167447-86167497	IMR90	lung:	fetal
5	chr4:86049133-86049183	SKMC	muscle:	n/a
6	chr4:86167398-86167448	NB4	blood:	n/a
7	chr4:86167398-86167448	RPTEC	kidney:	n/a
8	chr4:86224551-86224601	GM19239	blood:	n/a
9	chr4:86167447-86167497	GM12892	blood:	n/a
10	chr4:86049133-86049183	HCPEpiC	choroid plexus:	n/a
11	chr4:86224551-86224601	AG04450	lung:	fetal
12	chr4:86224551-86224601	HCPEpiC	choroid plexus:	n/a
13	chr4:86167398-86167448	NH-A	brain:	n/a
14	chr4:86049133-86049183	H1-hESC	embryonic stem cell:	embryo
15	chr4:86167398-86167448	SK-N-SH_RA	brain:	n/a
16	chr4:86167398-86167448	ECC-1	luminal epithelium:	n/a
17	chr4:86167398-86167448	SK-N-MC	brain:	n/a
18	chr4:86049133-86049183	HIPEpiC	eye:	n/a
19	chr4:86224551-86224601	NB4	blood:	n/a
20	chr4:86224551-86224601	HepG2	liver:	n/a
21	chr4:86167398-86167448	AG04450	lung:	fetal
22	chr4:86167447-86167497	HRE	kidney:	n/a
23	chr4:86224551-86224601	NT2-D1	testis:	n/a
24	chr4:86224551-86224601	ProgFib	skin:	n/a
25	chr4:86049133-86049183	AG09319	gingival:	n/a
26	chr4:86224551-86224601	HEK293	kidney:	embryo
27	chr4:86167447-86167497	NHBE	bronchial:	n/a
28	chr4:86224551-86224601	LNCaP	prostate:	n/a
29	chr4:86224551-86224601	GM12878	blood:	n/a
30	chr4:86167447-86167497	HCT-116	colon:	n/a
31	chr4:86167398-86167448	GM12892	blood:	n/a
32	chr4:86224551-86224601	NHDF-neo	bronchial:	n/a
33	chr4:86049133-86049183	MCF10A-Er-Src	breast:	n/a
34	chr4:86167447-86167497	BE2_C	brain:	n/a
35	chr4:86224551-86224601	Hepatocyte	liver:	n/a
36	chr4:86167447-86167497	GM06990	blood:	n/a
37	chr4:86224551-86224601	AoSMC	blood vessel:	n/a
38	chr4:86167447-86167497	AG04450	lung:	fetal
39	chr4:86224551-86224601	HRE	kidney:	n/a
40	chr4:86167447-86167497	HEEpiC	esophagus:	n/a
41	chr4:86167447-86167497	HNPCEpiC	eye:	n/a
42	chr4:86224551-86224601	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:86167447-86167497	CMK	blood:	n/a
44	chr4:86167398-86167448	Hela-S3	cervix:	n/a
45	chr4:86167398-86167448	HL-60	blood:	n/a
46	chr4:86167398-86167448	BE2_C	brain:	n/a
47	chr4:86167447-86167497	HEK293	kidney:	embryo
48	chr4:86167447-86167497	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:86167398-86167448	AG10803	skin:	n/a
50	chr4:86224551-86224601	HL-60	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:86003826..86005949-chr4:86016519..86019317,2	K562	blood:
2	chr4:86068352..86069122-chr4:86291595..86292351,2	MCF-7	breast:
3	chr16:71156761..71157534-chr4:86089661..86090552,2	MCF-7	breast:
4	chr4:86181906..86184238-chr4:86188477..86190210,2	MCF-7	breast:
5	chr4:85926409..85928748-chr4:85929559..85932473,2	MCF-7	breast:
6	chr4:86170923..86173404-chr4:86177410..86179415,2	K562	blood:
7	chr4:86068807..86069313-chr4:87816662..87817570,2	K562	blood:
8	chr4:86006119..86008878-chr4:86034902..86037833,2	K562	blood:
9	chr4:86070706..86072618-chr4:86075988..86078281,2	MCF-7	breast:
10	chr4:85924417..85926451-chr4:85927021..85928799,2	MCF-7	breast:
11	chr4:86180824..86182598-chr4:86183474..86185368,2	MCF-7	breast:
12	chr4:86153952..86155655-chr4:86156797..86158947,2	MCF-7	breast:
13	chr4:86234301..86236109-chr4:86239273..86242093,2	K562	blood:
14	chr4:86006119..86008878-chr4:86034902..86037833,2	K562	blood:
15	chr4:86100478..86103305-chr4:86104929..86106522,2	K562	blood:
16	chr4:86005492..86007740-chr4:86009347..86012181,2	MCF-7	breast:
17	chr4:86068287..86068959-chr4:86164739..86165523,2	MCF-7	breast:
18	chr4:85984391..85986077-chr4:85996497..85998865,2	K562	blood:
19	chr4:86005492..86007740-chr4:86009347..86012181,2	MCF-7	breast:
20	chr4:86048857..86049411-chr4:86239183..86239916,2	MCF-7	breast:
21	chr4:86003826..86005949-chr4:86016519..86019317,2	K562	blood:
22	chr4:86153952..86155655-chr4:86156797..86158947,2	MCF-7	breast:
23	chr4:86164928..86165741-chr4:86291153..86292328,4	MCF-7	breast:
24	chr4:85915588..85918291-chr4:85935086..85938051,2	K562	blood:
25	chr4:85984391..85986077-chr4:85996497..85998865,2	K562	blood:
26	chr4:86070706..86072618-chr4:86075988..86078281,2	MCF-7	breast:
27	chr4:86170923..86173404-chr4:86177410..86179415,2	K562	blood:
28	chr4:86068522..86069297-chr4:86668912..86669717,2	MCF-7	breast:
29	chr4:85926409..85928748-chr4:85929559..85932473,2	MCF-7	breast:
30	chr4:85924417..85926451-chr4:85927021..85928799,2	MCF-7	breast:
31	chr4:86068869..86069585-chr4:86668543..86669322,2	MCF-7	breast:
32	chr4:86180824..86182598-chr4:86183474..86185368,2	MCF-7	breast:
33	chr20:45985356..45987543-chr4:86157556..86159275,2	MCF-7	breast:
34	chr4:86181906..86184238-chr4:86188477..86190210,2	MCF-7	breast:
35	chr3:114101381..114101901-chr4:86005314..86006121,3	MCF-7	breast:
36	chr4:86129889..86132757-chr4:86146969..86148539,2	K562	blood:
37	chr4:86129889..86132757-chr4:86146969..86148539,2	K562	blood:
38	chr4:85927755..85929888-chr4:85933170..85935250,2	K562	blood:
39	chr4:85927755..85929888-chr4:85933170..85935250,2	K562	blood:
40	chr4:86100478..86103305-chr4:86104929..86106522,2	K562	blood:
41	chr4:86068287..86068959-chr4:86164739..86165523,2	MCF-7	breast:
42	chr4:86048857..86049411-chr4:86239183..86239916,2	MCF-7	breast:
43	chr4:85915588..85918291-chr4:85935086..85938051,2	K562	blood:
44	chr4:86234301..86236109-chr4:86239273..86242093,2	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDS1-2	chr4:85921840-85921918	NONHSAT097259
2	lnc-ARHGAP24-3	chr4:86144407-86144504	ucscGeneNc_uc003hpg_2
3	lnc-CDS1-2	chr4:85927165-85927467	NONHSAT097258
4	lnc-CDS1-2	chr4:85926627-85926721	ENSG00000180769
5	lnc-CDS1-2	chr4:85921844-85921918	ENSG00000180769
6	lnc-CDS1-2	chr4:85927160-85932430	ENSG00000180769
7	lnc-CDS1-2	chr4:85925383-85925480	ENSG00000180769
8	lnc-ARHGAP24-3	chr4:86109902-86110053	ucscGeneNc_uc003hpg_2
9	lnc-CDS1-2	chr4:85927160-85928168	NR_015359
10	lnc-CDS1-2	chr4:85927160-85928168	ENSG00000180769
11	lnc-ARHGAP24-3	chr4:86140868-86140942	ucscGeneNc_uc003hpg_2
12	lnc-ARHGAP24-3	chr4:86146184-86147192	ucscGeneNc_uc003hpg_2
13	lnc-CDS1-2	chr4:85927127-85929901	NONHSAT097259
14	lnc-ARHGAP24-4	chr4:86021649-86021976	NONHSAT097260
15	lnc-ARHGAP24-3	chr4:86145651-86145745	ucscGeneNc_uc003hpg_2
16	lnc-CDS1-2	chr4:85925383-85925480	NONHSAT097256
17	lnc-CDS1-2	chr4:85927160-85927748	NONHSAT097256
18	lnc-CDS1-2	chr4:85925383-85925480	NONHSAT097255
19	lnc-CDS1-2	chr4:85925383-85925482	NONHSAT097257
20	lnc-CDS1-2	chr4:85925383-85925480	NR_015359
21	lnc-CDS1-2	chr4:85925383-85925480	ENSG00000180769
22	lnc-CDS1-2	chr4:85927160-85928168	NONHSAT097255
23	lnc-CDS1-2	chr4:85925383-85925480	NONHSAT097258
24	lnc-ARHGAP24-3	chr4:86106995-86107304	ucscGeneNc_uc003hpg_2
25	lnc-CDS1-2	chr4:85925383-85925480	NONHSAT097259

No data

Variant related genes	Relation type
RN7SKP48	TF binding region
ENSG00000248725	TF binding region
RN7SKP48	CpG island
ENSG00000248725	CpG island
ENSG00000101040	chromatin interactions
FGF9	miRNA target sites
EGLN3	miRNA target sites
CHST12	miRNA target sites
CHST7	miRNA target sites
MED23	miRNA target sites
PKM2	miRNA target sites

Extended variants
information (count: 6424 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:6424 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543264382	chr4:85911043-85911044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113371053	chr4:85911047-85911048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561426022	chr4:85911049-85911050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576381831	chr4:85911165-85911166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111811122	chr4:85911192-85911193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs578024793	chr4:85911211-85911212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565358796	chr4:85911224-85911225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532443555	chr4:85911225-85911226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62303125	chr4:85911250-85911251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547503207	chr4:85911268-85911269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559877897	chr4:85911296-85911297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566585963	chr4:85911319-85911320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527488594	chr4:85911320-85911321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549259969	chr4:85911345-85911346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112442168	chr4:85911415-85911416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537829612	chr4:85911448-85911449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549537206	chr4:85911463-85911464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574010260	chr4:85911536-85911537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542939257	chr4:85911615-85911616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189719602	chr4:85911616-85911617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183475878	chr4:85911625-85911626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187709584	chr4:85911628-85911629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201935400	chr4:85911634-85911635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555228140	chr4:85911662-85911663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576693893	chr4:85911687-85911688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544118295	chr4:85911728-85911729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564902770	chr4:85911747-85911748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576837337	chr4:85911762-85911763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541081628	chr4:85911855-85911856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559469898	chr4:85911912-85911913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369356033	chr4:85911951-85911952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62303126	chr4:85911971-85911972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372667817	chr4:85911972-85911973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62303127	chr4:85911973-85911974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527474664	chr4:85912068-85912069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542488675	chr4:85912075-85912076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376863706	chr4:85912076-85912077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113698851	chr4:85912086-85912087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113246254	chr4:85912098-85912099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369926130	chr4:85912104-85912105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374426100	chr4:85912105-85912106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377683631	chr4:85912119-85912120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531476609	chr4:85912129-85912130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550064131	chr4:85912137-85912138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571221217	chr4:85912165-85912166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147280377	chr4:85912169-85912170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375365964	chr4:85912175-85912176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377578287	chr4:85912181-85912182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547512220	chr4:85912182-85912183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370639401	chr4:85912188-85912189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85906800-85927200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:85909200-85911600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:85913400-85926800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:85915000-85915800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr4:85915400-85915600	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr4:85915400-85915600	Active TSS	Rectal Smooth Muscle	rectum
7	chr4:85915400-85915600	Active TSS	Right Atrium	heart
8	chr4:85915400-85915800	Active TSS	H1 Cell Line	embryonic stem cell
9	chr4:85915400-85915800	Active TSS	Adipose Nuclei	Adipose
10	chr4:85915400-85915800	Active TSS	Aorta	Aorta
11	chr4:85915400-85915800	Active TSS	Brain Anterior Caudate	brain
12	chr4:85915400-85915800	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr4:85915400-85915800	Active TSS	Fetal Muscle Trunk	muscle
14	chr4:85915400-85915800	Active TSS	Fetal Muscle Leg	muscle
15	chr4:85915400-85915800	Enhancers	Right Ventricle	heart
16	chr4:85915400-85915800	Active TSS	Stomach Smooth Muscle	stomach
17	chr4:85915600-85915800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr4:85915600-85915800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:85915600-85915800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr4:85915600-85915800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:85915600-85915800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr4:85915600-85915800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr4:85915600-85915800	Enhancers	Psoas Muscle	Psoas
24	chr4:85915600-85915800	Flanking Active TSS	Rectal Smooth Muscle	rectum
25	chr4:85915600-85915800	Flanking Active TSS	Right Atrium	heart
26	chr4:85915600-85916000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr4:85915800-85916400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:85915800-85916800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:85915800-85916800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr4:85915800-85935600	Weak transcription	Aorta	Aorta
31	chr4:85916000-85917000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:85916200-85916600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:85916400-85917000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr4:85916600-85917200	Enhancers	HSMMtube	muscle
35	chr4:85916800-85917200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:85916800-85917200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:85916800-85917200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr4:85917000-85917200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:85917000-85918200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr4:85917200-85917400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:85917200-85919600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:85918200-85919000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr4:85925400-85935400	Weak transcription	Brain Hippocampus Middle	brain
44	chr4:85925400-85940600	Weak transcription	Left Ventricle	heart
45	chr4:85925600-85925800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:85925600-85928000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:85925800-85926400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:85925800-85932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr4:85926200-85927800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:85926200-85927800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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