Variant report

Variant	nsv874167
Chromosome Location	chr2:56284418-56388746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1141)
CpG islands
(count:183)
Chromatin interactive
region (count:42)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1141 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:56360713-56361628	K562	blood:	n/a	n/a
2	ARID3A	chr2:56359341-56359672	K562	blood:	n/a	n/a
3	ARID3A	chr2:56357648-56357918	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:56345293-56346040	K562	blood:	n/a	n/a
5	ARID3A	chr2:56359299-56359671	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:56357678-56357944	K562	blood:	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	chr2:56345528-56345845	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr2:56304682-56304972	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:56344590-56344790	K562	blood:	n/a	n/a
15	BHLHE40	chr2:56376113-56376321	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:56361155-56361204	K562	blood:	n/a	n/a
17	BHLHE40	chr2:56355091-56355163	K562	blood:	n/a	n/a
18	BHLHE40	chr2:56345522-56346047	K562	blood:	n/a	n/a
19	BHLHE40	chr2:56378263-56378301	A549	lung:	n/a	n/a
20	BHLHE40	chr2:56346957-56347152	K562	blood:	n/a	n/a
21	BHLHE40	chr2:56311315-56311590	K562	blood:	n/a	n/a
22	BHLHE40	chr2:56369951-56370064	K562	blood:	n/a	n/a
23	BHLHE40	chr2:56362106-56362195	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	chr2:56361253-56361453	K562	blood:	n/a	n/a
28	CCNT2	chr2:56369943-56370092	K562	blood:	n/a	n/a
29	CEBPB	chr2:56355437-56355687	H1-hESC	embryonic stem cell:	n/a	chr2:56355604-56355617
30	CEBPB	chr2:56317438-56317693	HepG2	liver:	n/a	chr2:56317567-56317578 chr2:56317549-56317560
31	CEBPB	chr2:56361164-56361329	K562	blood:	n/a	n/a
32	CEBPB	chr2:56357637-56358003	IMR90	lung:	n/a	n/a
33	CEBPB	chr2:56357651-56358058	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:56345603-56345983	K562	blood:	n/a	n/a
35	CEBPB	chr2:56357626-56357988	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:56354217-56354492	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:56299610-56299775	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:56317423-56317643	A549	lung:	n/a	chr2:56317567-56317578 chr2:56317549-56317560
39	CEBPB	chr2:56357608-56357972	K562	blood:	n/a	n/a
40	CEBPB	chr2:56354181-56354510	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:56357643-56357991	A549	lung:	n/a	n/a
42	CEBPB	chr2:56317539-56317669	H1-hESC	embryonic stem cell:	n/a	chr2:56317567-56317578 chr2:56317549-56317560
43	CEBPB	chr2:56355450-56355787	HepG2	liver:	n/a	chr2:56355604-56355617
44	CEBPB	chr2:56357630-56358013	A549	lung:	n/a	n/a
45	CEBPB	chr2:56357668-56357946	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:56304546-56304868	IMR90	lung:	n/a	chr2:56304685-56304696
47	CEBPB	chr2:56357632-56358009	K562	blood:	n/a	n/a
48	CEBPB	chr2:56355444-56355767	A549	lung:	n/a	chr2:56355604-56355617
49	CEBPB	chr2:56355429-56355769	K562	blood:	n/a	chr2:56355604-56355617
50	CEBPB	chr2:56304541-56304880	Hela-S3	cervix:	n/a	chr2:56304685-56304696

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:56318614-56318664	SK-N-MC	brain:	n/a
2	chr2:56318438-56318488	AG04449	skin:	fetal
3	chr2:56318614-56318664	AoSMC	blood vessel:	n/a
4	chr2:56346418-56346468	AG09309	skin:	n/a
5	chr2:56346418-56346468	GM12892	blood:	n/a
6	chr2:56318438-56318488	HepG2	liver:	n/a
7	chr2:56346418-56346468	IMR90	lung:	fetal
8	chr2:56346418-56346468	AG09319	gingival:	n/a
9	chr2:56318614-56318664	GM12878	blood:	n/a
10	chr2:56346418-56346468	HCT-116	colon:	n/a
11	chr2:56318614-56318664	HAEpiC	amniotic membrane:	n/a
12	chr2:56318438-56318488	PANC-1	pancreas:	n/a
13	chr2:56318438-56318488	HAEpiC	amniotic membrane:	n/a
14	chr2:56318614-56318664	LNCaP	prostate:	n/a
15	chr2:56318614-56318664	GM12891	blood:	n/a
16	chr2:56346418-56346468	HEK293	kidney:	embryo
17	chr2:56318438-56318488	HRPEpiC	eye:	n/a
18	chr2:56318438-56318488	NH-A	brain:	n/a
19	chr2:56318614-56318664	HCF	heart:	n/a
20	chr2:56318614-56318664	SAEC	small airway:	n/a
21	chr2:56318438-56318488	PFSK-1	brain:	n/a
22	chr2:56318438-56318488	AG09309	skin:	n/a
23	chr2:56318438-56318488	K562	blood:	n/a
24	chr2:56346418-56346468	HepG2	liver:	n/a
25	chr2:56318614-56318664	HCM	heart:	n/a
26	chr2:56318438-56318488	GM19239	blood:	n/a
27	chr2:56318614-56318664	T-47D	breast:	n/a
28	chr2:56346418-56346468	HNPCEpiC	eye:	n/a
29	chr2:56346418-56346468	HMEC	breast:	n/a
30	chr2:56318614-56318664	H1-hESC	embryonic stem cell:	embryo
31	chr2:56318614-56318664	Caco-2	colon:	n/a
32	chr2:56318614-56318664	GM12892	blood:	n/a
33	chr2:56346418-56346468	PFSK-1	brain:	n/a
34	chr2:56318614-56318664	K562	blood:	n/a
35	chr2:56318614-56318664	HRE	kidney:	n/a
36	chr2:56346418-56346468	HUVEC	blood vessel:	n/a
37	chr2:56318614-56318664	Jurkat	blood:	n/a
38	chr2:56346418-56346468	HRPEpiC	eye:	n/a
39	chr2:56346418-56346468	AoSMC	blood vessel:	n/a
40	chr2:56346418-56346468	HEEpiC	esophagus:	n/a
41	chr2:56318438-56318488	HEEpiC	esophagus:	n/a
42	chr2:56346418-56346468	T-47D	breast:	n/a
43	chr2:56346418-56346468	NHBE	bronchial:	n/a
44	chr2:56318614-56318664	GM06990	blood:	n/a
45	chr2:56318614-56318664	NB4	blood:	n/a
46	chr2:56318438-56318488	NHBE	bronchial:	n/a
47	chr2:56346418-56346468	AG04449	skin:	fetal
48	chr2:56346418-56346468	SKMC	muscle:	n/a
49	chr2:56346418-56346468	ProgFib	skin:	n/a
50	chr2:56346418-56346468	AG04450	lung:	fetal

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFEMP1-2	chr2:56301789-56305190	XLOC_002100
2	lnc-CCDC85A-2	chr2:56374765-56374879	NONHSAT070820
3	lnc-CCDC85A-2	chr2:56345217-56345306	NONHSAT070820
4	lnc-EFEMP1-2	chr2:56317445-56317517	ENSG00000229805
5	lnc-EFEMP1-2	chr2:56304552-56305190	ENSG00000229805
6	lnc-EFEMP1-2	chr2:56317445-56317514	NONHSAT070819
7	lnc-CCDC85A-2	chr2:56309504-56309580	ENSG00000272180.1
8	lnc-EFEMP1-2	chr2:56317445-56317511	XLOC_002100
9	lnc-EFEMP1-2	chr2:56301789-56305190	NONHSAT070819
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
ENSG00000229805	chromatin interactions
ENSG00000271894	chromatin interactions

Extended variants
information (count: 3107 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3107 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72798941	chr2:56301802-56301803	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564163395	chr2:56301814-56301815	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs552241561	chr2:56301896-56301897	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs369779058	chr2:56301924-56301925	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs112396518	chr2:56301929-56301930	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs72798942	chr2:56301975-56301976	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs554938703	chr2:56302070-56302071	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs200289158	chr2:56302074-56302075	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs36050410	chr2:56302081-56302082	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs568326835	chr2:56302098-56302099	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs373670262	chr2:56302154-56302155	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs537272284	chr2:56302218-56302219	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs556831189	chr2:56302228-56302229	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs576489454	chr2:56302229-56302230	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs185892023	chr2:56302253-56302254	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs188697368	chr2:56302258-56302259	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs138183996	chr2:56302287-56302288	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs76607550	chr2:56302288-56302289	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs561270476	chr2:56302311-56302312	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs530287009	chr2:56302358-56302359	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs372785659	chr2:56302380-56302381	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs528286595	chr2:56302421-56302422	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs77467754	chr2:56302438-56302439	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs529395412	chr2:56302513-56302514	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs76126948	chr2:56302539-56302540	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs532738170	chr2:56302561-56302562	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs575325920	chr2:56302613-56302614	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs181129172	chr2:56302625-56302626	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs186165925	chr2:56302630-56302631	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs528107851	chr2:56302647-56302648	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs147236664	chr2:56302827-56302828	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs377579624	chr2:56302831-56302832	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs139372695	chr2:56302858-56302859	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs536907571	chr2:56302859-56302860	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs533472182	chr2:56302890-56302891	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs546012063	chr2:56302891-56302892	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs557209309	chr2:56302904-56302905	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs569252379	chr2:56302920-56302921	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs548506329	chr2:56302936-56302937	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs539596915	chr2:56302950-56302951	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs115634280	chr2:56302970-56302971	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs561988981	chr2:56303032-56303033	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs564214123	chr2:56303068-56303069	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs541032385	chr2:56303076-56303077	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs72798943	chr2:56303122-56303123	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs574769700	chr2:56303135-56303136	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs543808396	chr2:56303150-56303151	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs190684109	chr2:56303195-56303196	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs371517672	chr2:56303198-56303199	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs184182651	chr2:56303210-56303211	Inactive region	lncRNA	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:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56309800-56310000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:56310000-56310200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:56310000-56313200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:56310400-56311400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:56310800-56312200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:56311000-56312000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:56311400-56311600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:56311400-56311600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:56311400-56311800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:56311400-56311800	Enhancers	Brain Substantia Nigra	brain
11	chr2:56311400-56311800	Enhancers	Fetal Heart	heart
12	chr2:56311400-56312000	Enhancers	Brain Hippocampus Middle	brain
13	chr2:56311600-56311800	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr2:56311600-56312000	Enhancers	HSMM	muscle
15	chr2:56311600-56312000	Enhancers	HSMMtube	muscle
16	chr2:56311800-56312800	Weak transcription	Fetal Heart	heart
17	chr2:56311800-56313000	Weak transcription	Brain Substantia Nigra	brain
18	chr2:56312000-56315400	Weak transcription	HSMM	muscle
19	chr2:56312200-56312600	Weak transcription	HSMMtube	muscle
20	chr2:56313200-56313400	Enhancers	Brain Substantia Nigra	brain
21	chr2:56313200-56313400	Enhancers	Pancreas	Pancrea
22	chr2:56313200-56313600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:56313200-56313600	Enhancers	Esophagus	oesophagus
24	chr2:56313400-56313600	Enhancers	Fetal Heart	heart
25	chr2:56315400-56315800	Enhancers	HSMM	muscle
26	chr2:56315600-56315800	Enhancers	HSMMtube	muscle
27	chr2:56315600-56316000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr2:56326000-56326400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr2:56326400-56327800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr2:56326800-56329200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:56327000-56327400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:56327200-56328000	Enhancers	Brain Hippocampus Middle	brain
33	chr2:56327800-56328000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr2:56327800-56328200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:56328000-56329000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:56328000-56334800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr2:56328200-56329600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:56328400-56328600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr2:56328400-56330000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr2:56328600-56328800	Enhancers	Fetal Heart	heart
41	chr2:56328600-56329800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr2:56328600-56329800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr2:56328800-56329000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:56329200-56329400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr2:56329200-56329600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:56329200-56329800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr2:56329400-56330000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr2:56329600-56330000	Enhancers	H1 Cell Line	embryonic stem cell
49	chr2:56329600-56330200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:56329600-56330200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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