Variant report

Variant	nsv874164
Chromosome Location	chr2:56280428-56388746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1177)
CpG islands
(count:183)
Chromatin interactive
region (count:43)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1177 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:56359299-56359671	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:56345293-56346040	K562	blood:	n/a	n/a
3	ARID3A	chr2:56360713-56361628	K562	blood:	n/a	n/a
4	ARID3A	chr2:56359341-56359672	K562	blood:	n/a	n/a
5	ARID3A	chr2:56357678-56357944	K562	blood:	n/a	n/a
6	ARID3A	chr2:56357648-56357918	HepG2	liver:	n/a	n/a
7	ATF1	chr2:56345600-56346004	K562	blood:	n/a	n/a
8	ATF2	chr2:56345691-56346081	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:56345577-56345997	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr2:56354256-56354419	K562	blood:	n/a	n/a
11	ATF3	chr2:56345664-56346130	K562	blood:	n/a	n/a
12	BACH1	chr2:56304682-56304972	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr2:56344590-56344790	K562	blood:	n/a	n/a
14	BACH1	chr2:56345528-56345845	H1-hESC	embryonic stem cell:	n/a	n/a
15	BHLHE40	chr2:56355091-56355163	K562	blood:	n/a	n/a
16	BHLHE40	chr2:56376113-56376321	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:56362106-56362195	K562	blood:	n/a	n/a
18	BHLHE40	chr2:56361155-56361204	K562	blood:	n/a	n/a
19	BHLHE40	chr2:56311315-56311590	K562	blood:	n/a	n/a
20	BHLHE40	chr2:56346957-56347152	K562	blood:	n/a	n/a
21	BHLHE40	chr2:56369951-56370064	K562	blood:	n/a	n/a
22	BHLHE40	chr2:56378263-56378301	A549	lung:	n/a	n/a
23	BHLHE40	chr2:56345522-56346047	K562	blood:	n/a	n/a
24	BRCA1	chr2:56357631-56357958	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr2:56369741-56370525	K562	blood:	n/a	n/a
26	CCNT2	chr2:56345804-56346573	K562	blood:	n/a	n/a
27	CCNT2	chr2:56369943-56370092	K562	blood:	n/a	n/a
28	CCNT2	chr2:56361253-56361453	K562	blood:	n/a	n/a
29	CEBPB	chr2:56354260-56354389	K562	blood:	n/a	n/a
30	CEBPB	chr2:56299610-56299775	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:56357608-56357972	K562	blood:	n/a	n/a
32	CEBPB	chr2:56304632-56304941	H1-hESC	embryonic stem cell:	n/a	chr2:56304685-56304696
33	CEBPB	chr2:56357651-56358058	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:56317506-56317623	Hela-S3	cervix:	n/a	chr2:56317567-56317578 chr2:56317549-56317560
35	CEBPB	chr2:56357632-56358009	K562	blood:	n/a	n/a
36	CEBPB	chr2:56354181-56354510	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:56357630-56358013	A549	lung:	n/a	n/a
38	CEBPB	chr2:56317539-56317669	H1-hESC	embryonic stem cell:	n/a	chr2:56317567-56317578 chr2:56317549-56317560
39	CEBPB	chr2:56329368-56329583	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr2:56357614-56358018	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:56317438-56317693	HepG2	liver:	n/a	chr2:56317567-56317578 chr2:56317549-56317560
42	CEBPB	chr2:56357540-56358110	A549	lung:	n/a	n/a
43	CEBPB	chr2:56355437-56355687	H1-hESC	embryonic stem cell:	n/a	chr2:56355604-56355617
44	CEBPB	chr2:56355444-56355767	A549	lung:	n/a	chr2:56355604-56355617
45	CEBPB	chr2:56357626-56357988	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr2:56354197-56354427	IMR90	lung:	n/a	n/a
47	CEBPB	chr2:56357705-56357919	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr2:56304559-56304786	A549	lung:	n/a	chr2:56304685-56304696
49	CEBPB	chr2:56304541-56304880	Hela-S3	cervix:	n/a	chr2:56304685-56304696
50	CEBPB	chr2:56357668-56357946	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:56346418-56346468	MCF10A-Er-Src	breast:	n/a
2	chr2:56318614-56318664	GM12878	blood:	n/a
3	chr2:56318614-56318664	NHBE	bronchial:	n/a
4	chr2:56318614-56318664	NB4	blood:	n/a
5	chr2:56318438-56318488	K562	blood:	n/a
6	chr2:56318438-56318488	NH-A	brain:	n/a
7	chr2:56346418-56346468	SK-N-MC	brain:	n/a
8	chr2:56318614-56318664	HRCEpiC	kidney:	n/a
9	chr2:56346418-56346468	NT2-D1	testis:	n/a
10	chr2:56318438-56318488	HMEC	breast:	n/a
11	chr2:56318438-56318488	AG10803	skin:	n/a
12	chr2:56318614-56318664	GM19239	blood:	n/a
13	chr2:56318438-56318488	MCF-7	breast:	n/a
14	chr2:56318614-56318664	BE2_C	brain:	n/a
15	chr2:56318614-56318664	HNPCEpiC	eye:	n/a
16	chr2:56318438-56318488	GM19239	blood:	n/a
17	chr2:56318614-56318664	IMR90	lung:	fetal
18	chr2:56318438-56318488	HRCEpiC	kidney:	n/a
19	chr2:56318614-56318664	NH-A	brain:	n/a
20	chr2:56318438-56318488	NHDF-neo	bronchial:	n/a
21	chr2:56346418-56346468	A549	lung:	n/a
22	chr2:56318614-56318664	HepG2	liver:	n/a
23	chr2:56346418-56346468	Caco-2	colon:	n/a
24	chr2:56346418-56346468	MCF-7	breast:	n/a
25	chr2:56318438-56318488	RPTEC	kidney:	n/a
26	chr2:56318614-56318664	HIPEpiC	eye:	n/a
27	chr2:56346418-56346468	BE2_C	brain:	n/a
28	chr2:56346418-56346468	SAEC	small airway:	n/a
29	chr2:56318614-56318664	Caco-2	colon:	n/a
30	chr2:56318438-56318488	HCT-116	colon:	n/a
31	chr2:56346418-56346468	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:56318438-56318488	PANC-1	pancreas:	n/a
33	chr2:56346418-56346468	GM06990	blood:	n/a
34	chr2:56318614-56318664	MCF10A-Er-Src	breast:	n/a
35	chr2:56318614-56318664	H1-hESC	embryonic stem cell:	embryo
36	chr2:56346418-56346468	PANC-1	pancreas:	n/a
37	chr2:56318614-56318664	SK-N-MC	brain:	n/a
38	chr2:56318614-56318664	ECC-1	luminal epithelium:	n/a
39	chr2:56318438-56318488	ProgFib	skin:	n/a
40	chr2:56346418-56346468	HepG2	liver:	n/a
41	chr2:56318614-56318664	SK-N-SH	brain:	n/a
42	chr2:56318438-56318488	LNCaP	prostate:	n/a
43	chr2:56318438-56318488	HCF	heart:	n/a
44	chr2:56318438-56318488	Hela-S3	cervix:	n/a
45	chr2:56318614-56318664	HUVEC	blood vessel:	n/a
46	chr2:56318614-56318664	RPTEC	kidney:	n/a
47	chr2:56318614-56318664	HRPEpiC	eye:	n/a
48	chr2:56318438-56318488	BE2_C	brain:	n/a
49	chr2:56318438-56318488	MCF10A-Er-Src	breast:	n/a
50	chr2:56346418-56346468	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:56304592..56305316-chr2:56360000..56360801,2	MCF-7	breast:
2	chr2:56343483..56346053-chr2:56349208..56350916,2	K562	blood:
3	chr2:56347349..56349192-chr2:56353229..56355396,2	K562	blood:
4	chr2:56387289..56389369-chr2:56393881..56395588,2	K562	blood:
5	chr2:56347349..56349192-chr2:56353229..56355396,2	K562	blood:
6	chr2:56347349..56350216-chr2:56353199..56356668,4	K562	blood:
7	chr2:56304415..56305097-chr2:56358925..56359914,3	MCF-7	breast:
8	chr2:56336331..56339032-chr2:56340759..56342871,3	K562	blood:
9	chr2:56337806..56341873-chr2:56342839..56347033,7	K562	blood:
10	chr2:56375448..56377112-chr2:56391906..56393998,2	K562	blood:
11	chr2:56304415..56305097-chr2:56358925..56359914,3	MCF-7	breast:
12	chr2:56308630..56311434-chr2:56349661..56352014,2	MCF-7	breast:
13	chr2:56337806..56342628-chr2:56343291..56347033,6	K562	blood:
14	chr2:56369334..56371717-chr2:56376735..56378498,2	K562	blood:
15	chr2:56308630..56311434-chr2:56349661..56352014,2	MCF-7	breast:
16	chr2:56275921..56278050-chr2:56279081..56281372,2	MCF-7	breast:
17	chr2:56304592..56305316-chr2:56360000..56360801,2	MCF-7	breast:
18	chr2:56369245..56372888-chr2:56373093..56376542,5	K562	blood:
19	chr2:56295326..56298009-chr2:56299848..56302574,2	MCF-7	breast:
20	chr2:56304414..56305364-chr2:56359067..56359975,5	K562	blood:
21	chr2:56347349..56350216-chr2:56353199..56356668,4	K562	blood:
22	chr2:56304295..56305416-chr2:56357297..56358336,5	MCF-7	breast:
23	chr2:56338244..56341178-chr2:56349675..56352414,2	MCF-7	breast:
24	chr2:56342001..56344983-chr2:56348767..56350916,2	K562	blood:
25	chr2:56370169..56372361-chr2:56373050..56375591,3	K562	blood:
26	chr2:56304414..56305364-chr2:56359067..56359975,5	K562	blood:
27	chr2:56310406..56312989-chr2:56352188..56354014,2	MCF-7	breast:
28	chr2:56295326..56298009-chr2:56299848..56302574,2	MCF-7	breast:
29	chr2:56343483..56346053-chr2:56349208..56350916,2	K562	blood:
30	chr2:56315975..56318654-chr2:56340489..56342924,2	K562	blood:
31	chr2:56369334..56371717-chr2:56376735..56378498,2	K562	blood:
32	chr2:56336331..56339032-chr2:56340759..56342871,3	K562	blood:
33	chr2:56352055..56354777-chr2:56356409..56359024,3	K562	blood:
34	chr2:56338244..56341178-chr2:56349675..56352414,2	MCF-7	breast:
35	chr2:56352055..56354777-chr2:56356409..56359024,3	K562	blood:
36	chr2:56310406..56312989-chr2:56352188..56354014,2	MCF-7	breast:
37	chr2:56357220..56358069-chr2:57743520..57744164,2	MCF-7	breast:
38	chr2:56304295..56305416-chr2:56357297..56358336,5	MCF-7	breast:
39	chr2:56373950..56376355-chr2:56383200..56384909,2	MCF-7	breast:
40	chr2:56337806..56341873-chr2:56342839..56347033,7	K562	blood:
41	chr2:56342001..56344983-chr2:56348767..56350916,2	K562	blood:
42	chr2:55914359..55914875-chr2:56359733..56360705,2	MCF-7	breast:
43	chr2:56337806..56342628-chr2:56343291..56347033,6	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFEMP1-2	chr2:56317445-56317514	NONHSAT070819
2	lnc-EFEMP1-2	chr2:56301789-56305190	XLOC_002100
3	lnc-CCDC85A-2	chr2:56345217-56345306	NONHSAT070820
4	lnc-CCDC85A-2	chr2:56374765-56374879	NONHSAT070820
5	lnc-EFEMP1-2	chr2:56301789-56305190	NONHSAT070819
6	lnc-CCDC85A-2	chr2:56309504-56309580	ENSG00000272180.1
7	lnc-EFEMP1-2	chr2:56317445-56317511	XLOC_002100
8	lnc-EFEMP1-2	chr2:56317445-56317517	ENSG00000229805
9	lnc-EFEMP1-2	chr2:56304552-56305190	ENSG00000229805
10	lnc-CCDC85A-2	chr2:56374765-56374875	ENSG00000272180.1

No data

Variant related genes	Relation type
ENSG00000229805	TF binding region
ENSG00000271894	TF binding region
ENSG00000229805	CpG island
ENSG00000271894	CpG island
ENSG00000271894	chromatin interactions
ENSG00000229805	chromatin interactions

Extended variants
information (count: 3176 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3176 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs891881	chr2:56280428-56280429	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183400918	chr2:56280495-56280496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187940099	chr2:56280514-56280515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201071433	chr2:56280535-56280536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551207145	chr2:56280557-56280558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571053723	chr2:56280634-56280635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533606287	chr2:56280644-56280645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192807412	chr2:56280664-56280665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576277165	chr2:56280694-56280695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561156923	chr2:56280703-56280704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115959664	chr2:56280721-56280722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182308035	chr2:56280751-56280752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535513101	chr2:56280886-56280887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373336333	chr2:56280887-56280888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149882597	chr2:56280889-56280890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537755038	chr2:56280975-56280976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369383496	chr2:56280995-56280996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558082135	chr2:56281017-56281018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143857951	chr2:56281122-56281123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372995537	chr2:56281131-56281132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533773523	chr2:56281133-56281134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144554322	chr2:56281137-56281138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569891624	chr2:56281138-56281139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186626834	chr2:56281150-56281151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111489222	chr2:56281156-56281157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537581992	chr2:56281175-56281176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541879611	chr2:56281201-56281202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557847717	chr2:56281208-56281209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147848385	chr2:56281260-56281261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192559834	chr2:56281270-56281271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544271125	chr2:56281378-56281379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17047452	chr2:56281390-56281391	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs368961294	chr2:56281400-56281401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373578511	chr2:56282404-56282405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556060073	chr2:56282437-56282438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74378162	chr2:56282441-56282442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537916392	chr2:56282442-56282443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371551319	chr2:56282443-56282444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558190911	chr2:56282455-56282456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181103065	chr2:56282482-56282483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374665685	chr2:56282504-56282505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs578175384	chr2:56282516-56282517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554548803	chr2:56282546-56282547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77893707	chr2:56282566-56282567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543233946	chr2:56282568-56282569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562913454	chr2:56282680-56282681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531453072	chr2:56282754-56282755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11693561	chr2:56282762-56282763	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs564634778	chr2:56282819-56282820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527327039	chr2:56282876-56282877	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56272000-56281400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:56276800-56280600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:56280600-56281200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:56280600-56281400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:56280800-56281400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:56282400-56283400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr2:56309800-56310000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:56310000-56310200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:56310000-56313200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:56310400-56311400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:56310800-56312200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:56311000-56312000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:56311400-56311600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr2:56311400-56311600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr2:56311400-56311800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:56311400-56311800	Enhancers	Brain Substantia Nigra	brain
17	chr2:56311400-56311800	Enhancers	Fetal Heart	heart
18	chr2:56311400-56312000	Enhancers	Brain Hippocampus Middle	brain
19	chr2:56311600-56311800	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr2:56311600-56312000	Enhancers	HSMM	muscle
21	chr2:56311600-56312000	Enhancers	HSMMtube	muscle
22	chr2:56311800-56312800	Weak transcription	Fetal Heart	heart
23	chr2:56311800-56313000	Weak transcription	Brain Substantia Nigra	brain
24	chr2:56312000-56315400	Weak transcription	HSMM	muscle
25	chr2:56312200-56312600	Weak transcription	HSMMtube	muscle
26	chr2:56313200-56313400	Enhancers	Brain Substantia Nigra	brain
27	chr2:56313200-56313400	Enhancers	Pancreas	Pancrea
28	chr2:56313200-56313600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:56313200-56313600	Enhancers	Esophagus	oesophagus
30	chr2:56313400-56313600	Enhancers	Fetal Heart	heart
31	chr2:56315400-56315800	Enhancers	HSMM	muscle
32	chr2:56315600-56315800	Enhancers	HSMMtube	muscle
33	chr2:56315600-56316000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr2:56326000-56326400	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr2:56326400-56327800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr2:56326800-56329200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:56327000-56327400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:56327200-56328000	Enhancers	Brain Hippocampus Middle	brain
39	chr2:56327800-56328000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr2:56327800-56328200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr2:56328000-56329000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr2:56328000-56334800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr2:56328200-56329600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr2:56328400-56328600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr2:56328400-56330000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr2:56328600-56328800	Enhancers	Fetal Heart	heart
47	chr2:56328600-56329800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr2:56328600-56329800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr2:56328800-56329000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:56329200-56329400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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