Variant report

Variant	nsv999571
Chromosome Location	chr2:53690538-53775723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:684)
CpG islands
(count:366)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:53718011-53718202	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:53743884-53744091	GM12878	blood:	n/a	n/a
3	BATF	chr2:53743872-53744174	GM12878	blood:	n/a	n/a
4	BRCA1	chr2:53703941-53704510	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr2:53739626-53739837	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr2:53702397-53703247	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr2:53732954-53733393	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr2:53701938-53703325	HCT-116	colon:	n/a	n/a
9	CBX3	chr2:53702123-53703068	HCT-116	colon:	n/a	n/a
10	CBX3	chr2:53703850-53704480	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:53720034-53720332	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:53742616-53743191	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:53702175-53703286	Hela-S3	cervix:	n/a	chr2:53703002-53703019
14	CEBPB	chr2:53725295-53725758	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr2:53702263-53703112	HCT-116	colon:	n/a	chr2:53703002-53703019
16	CEBPB	chr2:53725272-53725726	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:53703905-53704648	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:53739537-53739943	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:53743586-53743649	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:53752634-53752730	K562	blood:	n/a	n/a
21	CEBPB	chr2:53739555-53739944	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:53717911-53718214	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:53717882-53718254	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:53700457-53700739	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:53701031-53701420	Hela-S3	cervix:	n/a	chr2:53701315-53701327
26	CEBPB	chr2:53702219-53703198	HCT-116	colon:	n/a	chr2:53703002-53703019
27	CEBPB	chr2:53739612-53739812	HepG2	liver:	n/a	n/a
28	CHD1	chr2:53696089-53696141	GM12878	blood:	n/a	n/a
29	CHD2	chr2:53702154-53703199	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr2:53703925-53704545	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr2:53739624-53739824	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr2:53732991-53733366	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr2:53700516-53700716	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr2:53700508-53700694	GM12878	blood:	n/a	n/a
35	CTCF	chr2:53738876-53738975	MCF-7	breast:	n/a	chr2:53738900-53738907
36	CTCF	chr2:53735900-53736050	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr2:53700540-53700690	HCT-116	colon:	n/a	n/a
38	CTCF	chr2:53742940-53743090	NHEK	skin:	n/a	n/a
39	CTCF	chr2:53742948-53743174	NHEK	skin:	n/a	n/a
40	CTCF	chr2:53697000-53697150	GM12874	blood:	n/a	n/a
41	CTCF	chr2:53742960-53743110	HEK293	kidney:	n/a	n/a
42	CTCF	chr2:53700537-53700639	Medullo	brain:	n/a	n/a
43	CTCF	chr2:53700481-53700629	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr2:53742980-53743130	RPTEC	kidney:	n/a	n/a
45	CTCF	chr2:53735860-53736010	HMF	breast:	n/a	n/a
46	CTCF	chr2:53742960-53743110	Caco-2	colon:	n/a	n/a
47	CTCF	chr2:53700446-53700741	MCF-7	breast:	n/a	n/a
48	CTCF	chr2:53742980-53743130	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr2:53700465-53700711	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:53700560-53700710	A549	lung:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53714365-53714415	BJ	skin:	n/a
2	chr2:53764920-53764970	HEEpiC	esophagus:	n/a
3	chr2:53725202-53725252	A549	lung:	n/a
4	chr2:53725202-53725252	HCM	heart:	n/a
5	chr2:53714365-53714415	Hepatocyte	liver:	n/a
6	chr2:53701531-53701581	Jurkat	blood:	n/a
7	chr2:53731598-53731648	GM12892	blood:	n/a
8	chr2:53764920-53764970	AG04449	skin:	fetal
9	chr2:53747541-53747591	GM12878	blood:	n/a
10	chr2:53701531-53701581	RPTEC	kidney:	n/a
11	chr2:53714365-53714415	LNCaP	prostate:	n/a
12	chr2:53701531-53701581	HMEC	breast:	n/a
13	chr2:53701531-53701581	AG04450	lung:	fetal
14	chr2:53731598-53731648	H1-hESC	embryonic stem cell:	embryo
15	chr2:53747541-53747591	NB4	blood:	n/a
16	chr2:53747541-53747591	GM06990	blood:	n/a
17	chr2:53747541-53747591	HAEpiC	amniotic membrane:	n/a
18	chr2:53731598-53731648	BE2_C	brain:	n/a
19	chr2:53701531-53701581	SAEC	small airway:	n/a
20	chr2:53764920-53764970	U87	brain:	n/a
21	chr2:53764920-53764970	Caco-2	colon:	n/a
22	chr2:53725202-53725252	Jurkat	blood:	n/a
23	chr2:53764920-53764970	NB4	blood:	n/a
24	chr2:53747541-53747591	HUVEC	blood vessel:	n/a
25	chr2:53764920-53764970	AoSMC	blood vessel:	n/a
26	chr2:53714365-53714415	NHDF-neo	bronchial:	n/a
27	chr2:53701531-53701581	CMK	blood:	n/a
28	chr2:53714365-53714415	PrEC	prostate:	n/a
29	chr2:53747541-53747591	Hepatocyte	liver:	n/a
30	chr2:53764920-53764970	Jurkat	blood:	n/a
31	chr2:53747541-53747591	AG04450	lung:	fetal
32	chr2:53731598-53731648	AG04450	lung:	fetal
33	chr2:53714365-53714415	SK-N-MC	brain:	n/a
34	chr2:53701531-53701581	PANC-1	pancreas:	n/a
35	chr2:53764920-53764970	Hela-S3	cervix:	n/a
36	chr2:53764920-53764970	HEK293	kidney:	embryo
37	chr2:53731598-53731648	GM19239	blood:	n/a
38	chr2:53764920-53764970	HMEC	breast:	n/a
39	chr2:53725202-53725252	CMK	blood:	n/a
40	chr2:53725202-53725252	HCPEpiC	choroid plexus:	n/a
41	chr2:53764920-53764970	NT2-D1	testis:	n/a
42	chr2:53764920-53764970	MCF10A-Er-Src	breast:	n/a
43	chr2:53764920-53764970	ECC-1	luminal epithelium:	n/a
44	chr2:53764920-53764970	NH-A	brain:	n/a
45	chr2:53701531-53701581	U87	brain:	n/a
46	chr2:53714365-53714415	HCM	heart:	n/a
47	chr2:53725202-53725252	HIPEpiC	eye:	n/a
48	chr2:53714365-53714415	HL-60	blood:	n/a
49	chr2:53714365-53714415	AG04449	skin:	fetal
50	chr2:53764920-53764970	HepG2	liver:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:53720586..53722714-chr2:53727046..53728819,2	MCF-7	breast:
2	chr2:53203292..53203812-chr2:53700344..53701275,2	MCF-7	breast:
3	chr2:53691365..53693137-chr2:53701304..53703137,2	MCF-7	breast:
4	chr2:53763474..53765231-chr2:53774418..53775976,2	K562	blood:
5	chr2:53757085..53758831-chr2:53762624..53764865,2	K562	blood:
6	chr2:53718351..53720003-chr2:53723225..53725281,2	K562	blood:
7	chr2:53725082..53727239-chr2:53732255..53735113,2	K562	blood:
8	chr2:53691365..53693137-chr2:53701304..53703137,2	MCF-7	breast:
9	chr2:53764669..53766504-chr2:53770937..53773630,2	K562	blood:
10	chr2:53720586..53722714-chr2:53727046..53728819,2	MCF-7	breast:
11	chr2:53687502..53690121-chr2:53692072..53694054,2	K562	blood:
12	chr2:53763474..53765231-chr2:53774418..53775976,2	K562	blood:
13	chr2:53771758..53774525-chr2:53776196..53777860,2	MCF-7	breast:
14	chr2:53764669..53766504-chr2:53770937..53773630,2	K562	blood:
15	chr2:53774246..53775776-chr2:53777337..53778910,2	K562	blood:
16	chr2:53725082..53727239-chr2:53732255..53735113,2	K562	blood:
17	chr2:53757085..53758831-chr2:53762624..53764865,2	K562	blood:
18	chr2:53718351..53720003-chr2:53723225..53725281,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000223897	TF binding region
ENSG00000251942	TF binding region
ENSG00000223897	CpG island
ENSG00000251942	CpG island

Extended variants
information (count: 3434 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3434 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7565178	chr2:53690569-53690570	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559830066	chr2:53690605-53690606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528465347	chr2:53690657-53690658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534341323	chr2:53690664-53690665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150447071	chr2:53690669-53690670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547976407	chr2:53690696-53690697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567800318	chr2:53690739-53690740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184691660	chr2:53690768-53690769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556620623	chr2:53690771-53690772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548608808	chr2:53690857-53690858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538670859	chr2:53690912-53690913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571917407	chr2:53690918-53690919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558582551	chr2:53690970-53690971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534189561	chr2:53690971-53690972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141386045	chr2:53690973-53690974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189476044	chr2:53690984-53690985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554364246	chr2:53691002-53691003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559840493	chr2:53691010-53691011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560292065	chr2:53691015-53691016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192526197	chr2:53691030-53691031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542891521	chr2:53691033-53691034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145171926	chr2:53691154-53691155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531304334	chr2:53691156-53691157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184170087	chr2:53691191-53691192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190313056	chr2:53691239-53691240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs80098551	chr2:53691240-53691241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138940449	chr2:53691244-53691245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547219731	chr2:53691277-53691278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs745685	chr2:53691289-53691290	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571578433	chr2:53691311-53691312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571076750	chr2:53691320-53691321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536464566	chr2:53691343-53691344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140652012	chr2:53691420-53691421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570018588	chr2:53691476-53691477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114158850	chr2:53691494-53691495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558519557	chr2:53691517-53691518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150464963	chr2:53691521-53691522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535096071	chr2:53691611-53691612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181164245	chr2:53691612-53691613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71413234	chr2:53691617-53691618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186714337	chr2:53691622-53691623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575365653	chr2:53691666-53691667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542476781	chr2:53691671-53691672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551977256	chr2:53691683-53691684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576411564	chr2:53691688-53691689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545360006	chr2:53691690-53691691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564867230	chr2:53691691-53691692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370859332	chr2:53691700-53691701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565816764	chr2:53691707-53691708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1565800	chr2:53691711-53691712	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

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
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	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
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53689400-53690600	Weak transcription	Fetal Brain Male	brain
2	chr2:53690000-53691000	Weak transcription	Fetal Heart	heart
3	chr2:53690400-53691800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr2:53690600-53692200	Enhancers	Fetal Brain Male	brain
5	chr2:53690800-53692000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:53691000-53692000	Enhancers	Fetal Heart	heart
7	chr2:53691400-53691800	Enhancers	Brain Anterior Caudate	brain
8	chr2:53691800-53692200	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr2:53694600-53695400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr2:53694600-53695400	Enhancers	Brain Germinal Matrix	brain
11	chr2:53694800-53695000	Enhancers	Fetal Kidney	kidney
12	chr2:53697600-53698000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr2:53697600-53698200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:53697600-53698200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:53697600-53698200	Enhancers	HMEC	breast
16	chr2:53697600-53698200	Enhancers	NHEK	skin
17	chr2:53698000-53698200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr2:53698000-53706400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:53698200-53700400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr2:53698200-53702200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr2:53698200-53702200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:53698200-53702200	Weak transcription	HMEC	breast
23	chr2:53698200-53702200	Weak transcription	NHEK	skin
24	chr2:53700000-53703000	Enhancers	Hela-S3	cervix
25	chr2:53700200-53700800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:53700400-53700600	Enhancers	NH-A	brain
27	chr2:53700400-53700600	Enhancers	NHLF	lung
28	chr2:53700400-53701200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:53700400-53701200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:53700400-53704200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:53700800-53701000	Enhancers	NHDF-Ad	bronchial
32	chr2:53700800-53702400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr2:53701000-53702000	Weak transcription	NHDF-Ad	bronchial
34	chr2:53701000-53702200	Weak transcription	NHLF	lung
35	chr2:53701200-53702200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:53701200-53704000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:53702000-53703200	Enhancers	NHDF-Ad	bronchial
38	chr2:53702200-53702600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:53702200-53703200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr2:53702200-53703200	Enhancers	A549	lung
41	chr2:53702200-53703200	Enhancers	NHLF	lung
42	chr2:53702200-53703400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:53702200-53703600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:53702200-53703600	Enhancers	NH-A	brain
45	chr2:53702200-53704000	Enhancers	HMEC	breast
46	chr2:53702200-53704200	Enhancers	NHEK	skin
47	chr2:53702400-53702600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:53702400-53703200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:53702600-53703000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr2:53703000-53703200	Flanking Active TSS	Hela-S3	cervix

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