Variant report

Variant	nsv874110
Chromosome Location	chr2:52383698-52582535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:52467445-52467547	K562	blood:	n/a	n/a
2	BACH1	chr2:52565069-52565261	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:52562997-52563330	H1-hESC	embryonic stem cell:	n/a	chr2:52563100-52563114
4	BRCA1	chr2:52412674-52412755	GM12878	blood:	n/a	n/a
5	CBX3	chr2:52554738-52555164	HCT-116	colon:	n/a	n/a
6	CEBPB	chr2:52424527-52424851	IMR90	lung:	n/a	chr2:52424680-52424691
7	CEBPB	chr2:52562807-52563121	A549	lung:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
8	CEBPB	chr2:52484592-52484943	HepG2	liver:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
9	CEBPB	chr2:52562730-52563288	ECC-1	luminal epithelium:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52563266-52563277 chr2:52562956-52562967
10	CEBPB	chr2:52488046-52488388	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:52570208-52570547	Hela-S3	cervix:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
12	CEBPB	chr2:52516875-52517234	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr2:52484597-52484933	IMR90	lung:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
14	CEBPB	chr2:52569536-52570532	IMR90	lung:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
15	CEBPB	chr2:52562815-52563192	IMR90	lung:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
16	CEBPB	chr2:52508157-52508457	HepG2	liver:	n/a	chr2:52508316-52508327
17	CEBPB	chr2:52568912-52569271	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:52424578-52424825	A549	lung:	n/a	chr2:52424680-52424691
19	CEBPB	chr2:52508166-52508428	IMR90	lung:	n/a	chr2:52508316-52508327
20	CEBPB	chr2:52562704-52563282	ECC-1	luminal epithelium:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52563266-52563277 chr2:52562956-52562967
21	CEBPB	chr2:52447440-52447956	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr2:52497321-52497563	HepG2	liver:	n/a	chr2:52497433-52497444
23	CEBPB	chr2:52570175-52570518	H1-hESC	embryonic stem cell:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
24	CEBPB	chr2:52516417-52516634	HepG2	liver:	n/a	chr2:52516470-52516481
25	CEBPB	chr2:52570199-52570514	A549	lung:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
26	CEBPB	chr2:52562773-52563118	HepG2	liver:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
27	CEBPB	chr2:52475213-52475267	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr2:52516890-52517212	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:52570882-52571236	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr2:52437849-52438049	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:52569009-52569163	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:52568887-52569285	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:52562875-52563266	H1-hESC	embryonic stem cell:	n/a	chr2:52562955-52562968 chr2:52563083-52563094 chr2:52562956-52562967
34	CEBPB	chr2:52475235-52475401	A549	lung:	n/a	chr2:52475269-52475280
35	CEBPB	chr2:52496637-52496874	HepG2	liver:	n/a	chr2:52496760-52496771
36	CEBPB	chr2:52424565-52424782	Hela-S3	cervix:	n/a	chr2:52424680-52424691
37	CEBPB	chr2:52475176-52475438	HepG2	liver:	n/a	chr2:52475269-52475280
38	CEBPB	chr2:52434940-52435407	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:52493705-52493946	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:52484634-52484917	A549	lung:	n/a	chr2:52484762-52484773 chr2:52484763-52484772 chr2:52484761-52484774 chr2:52484761-52484772
41	CEBPB	chr2:52424571-52424862	HepG2	liver:	n/a	chr2:52424680-52424691
42	CEBPB	chr2:52570177-52570534	HepG2	liver:	n/a	chr2:52570356-52570367 chr2:52570358-52570367 chr2:52570356-52570369 chr2:52570358-52570367 chr2:52570358-52570367
43	CEBPB	chr2:52447446-52447926	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr2:52496591-52497101	IMR90	lung:	n/a	chr2:52496760-52496771
45	CEBPB	chr2:52496622-52496897	A549	lung:	n/a	chr2:52496760-52496771
46	CEBPB	chr2:52516375-52516634	IMR90	lung:	n/a	chr2:52516470-52516481
47	CHD2	chr2:52480885-52480914	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr2:52491760-52491910	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr2:52456901-52457018	GM19239	blood:	n/a	n/a
50	CTCF	chr2:52535760-52535910	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52571550-52571600	NB4	blood:	n/a
2	chr2:52480467-52480517	Hela-S3	cervix:	n/a
3	chr2:52480467-52480517	AoSMC	blood vessel:	n/a
4	chr2:52571550-52571600	HIPEpiC	eye:	n/a
5	chr2:52571550-52571600	AG09309	skin:	n/a
6	chr2:52571550-52571600	HMEC	breast:	n/a
7	chr2:52480467-52480517	GM12892	blood:	n/a
8	chr2:52480467-52480517	GM19239	blood:	n/a
9	chr2:52480467-52480517	GM12878	blood:	n/a
10	chr2:52571550-52571600	PFSK-1	brain:	n/a
11	chr2:52480467-52480517	MCF-7	breast:	n/a
12	chr2:52480467-52480517	IMR90	lung:	fetal
13	chr2:52480467-52480517	AG09309	skin:	n/a
14	chr2:52571550-52571600	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:52571550-52571600	LNCaP	prostate:	n/a
16	chr2:52480467-52480517	HIPEpiC	eye:	n/a
17	chr2:52480467-52480517	H1-hESC	embryonic stem cell:	embryo
18	chr2:52480467-52480517	HRE	kidney:	n/a
19	chr2:52480467-52480517	Hepatocyte	liver:	n/a
20	chr2:52480467-52480517	SK-N-SH_RA	brain:	n/a
21	chr2:52571550-52571600	GM12878	blood:	n/a
22	chr2:52571550-52571600	Hela-S3	cervix:	n/a
23	chr2:52480467-52480517	SK-N-MC	brain:	n/a
24	chr2:52571550-52571600	HEEpiC	esophagus:	n/a
25	chr2:52571550-52571600	Caco-2	colon:	n/a
26	chr2:52571550-52571600	AG10803	skin:	n/a
27	chr2:52571550-52571600	T-47D	breast:	n/a
28	chr2:52571550-52571600	HCPEpiC	choroid plexus:	n/a
29	chr2:52480467-52480517	HepG2	liver:	n/a
30	chr2:52480467-52480517	HCPEpiC	choroid plexus:	n/a
31	chr2:52480467-52480517	BE2_C	brain:	n/a
32	chr2:52480467-52480517	HCF	heart:	n/a
33	chr2:52480467-52480517	ECC-1	luminal epithelium:	n/a
34	chr2:52571550-52571600	H1-hESC	embryonic stem cell:	embryo
35	chr2:52480467-52480517	HCT-116	colon:	n/a
36	chr2:52571550-52571600	MCF-7	breast:	n/a
37	chr2:52571550-52571600	NH-A	brain:	n/a
38	chr2:52480467-52480517	GM06990	blood:	n/a
39	chr2:52571550-52571600	AoSMC	blood vessel:	n/a
40	chr2:52480467-52480517	PrEC	prostate:	n/a
41	chr2:52480467-52480517	LNCaP	prostate:	n/a
42	chr2:52571550-52571600	NHDF-neo	bronchial:	n/a
43	chr2:52571550-52571600	SK-N-SH	brain:	n/a
44	chr2:52480467-52480517	SKMC	muscle:	n/a
45	chr2:52480467-52480517	HRPEpiC	eye:	n/a
46	chr2:52571550-52571600	CMK	blood:	n/a
47	chr2:52571550-52571600	SKMC	muscle:	n/a
48	chr2:52480467-52480517	PFSK-1	brain:	n/a
49	chr2:52571550-52571600	NT2-D1	testis:	n/a
50	chr2:52480467-52480517	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:52521422..52524399-chr2:52528510..52532522,3	K562	blood:
2	chr2:52476747..52479271-chr2:52487226..52489997,2	K562	blood:
3	chr2:52476747..52479271-chr2:52487226..52489997,2	K562	blood:
4	chr2:52444137..52446093-chr2:52447228..52448981,2	K562	blood:
5	chr2:52444137..52446093-chr2:52447228..52448981,2	K562	blood:
6	chr2:52521422..52524399-chr2:52528510..52532522,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-11	chr2:52575330-52575504	NONHSAT070669
2	lnc-CHAC2-4	chr2:52543370-52543438	ENSG00000231918.1
3	lnc-CHAC2-10	chr2:52470105-52470654	NONHSAT070667
4	lnc-ASB3-11	chr2:52576407-52576478	NONHSAT070669
5	lnc-ASB3-11	chr2:52579245-52579427	NONHSAT070669
6	lnc-CHAC2-10	chr2:52453760-52453813	NONHSAT070667
7	lnc-CHAC2-4	chr2:52580012-52580100	ENSG00000231918.1
8	lnc-ASB3-11	chr2:52581186-52581394	NONHSAT070669
9	lnc-CHAC2-4	chr2:52576463-52578424	ENSG00000231918.1

Variant related genes	Relation type
ENSG00000202195	TF binding region
ENSG00000202195	CpG island

Extended variants
information (count: 3760 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3760 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574241673	chr2:52385216-52385217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543338603	chr2:52385256-52385257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191239280	chr2:52385295-52385296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575216459	chr2:52385326-52385327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180754662	chr2:52385347-52385348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185080339	chr2:52385356-52385357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551360131	chr2:52385368-52385369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190734074	chr2:52385376-52385377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546388035	chr2:52385388-52385389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559957949	chr2:52385389-52385390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567455370	chr2:52385394-52385395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368871532	chr2:52385404-52385405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549290558	chr2:52385414-52385415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114950098	chr2:52385425-52385426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115940773	chr2:52385458-52385459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538065805	chr2:52385461-52385462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559603040	chr2:52385467-52385468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550022599	chr2:52385477-52385478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7349359	chr2:52385489-52385490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369826612	chr2:52385541-52385542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571763729	chr2:52385577-52385578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183202653	chr2:52385580-52385581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554389681	chr2:52385584-52385585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369870216	chr2:52385585-52385586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574204720	chr2:52385641-52385642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536515959	chr2:52385657-52385658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556832126	chr2:52385658-52385659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571421691	chr2:52385696-52385697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115640387	chr2:52385697-52385698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149768274	chr2:52385714-52385715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374277908	chr2:52385745-52385746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12476761	chr2:52385756-52385757	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370449771	chr2:52385778-52385779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145777413	chr2:52385840-52385841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77260916	chr2:52385883-52385884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560071207	chr2:52385951-52385952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529109933	chr2:52385962-52385963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35886094	chr2:52385964-52385965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372607772	chr2:52386006-52386007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11675869	chr2:52386032-52386033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542513512	chr2:52386037-52386038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1922201	chr2:52386043-52386044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs187937400	chr2:52386077-52386078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1922202	chr2:52386104-52386105	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs148954946	chr2:52386110-52386111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12477631	chr2:52386144-52386145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs191741897	chr2:52386158-52386159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs117203182	chr2:52386166-52386167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375924649	chr2:52386175-52386176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368539778	chr2:52386180-52386181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
small cell lung cancer	20016488	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
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52385200-52385800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:52385800-52389800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:52389200-52389600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr2:52389200-52389600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr2:52389800-52390000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:52408000-52408400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr2:52408000-52408400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:52412800-52413000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:52419200-52419400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:52419200-52421200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr2:52419200-52421200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:52419400-52420400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr2:52420400-52421600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:52427600-52427800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:52434800-52435000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:52435000-52435200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:52435200-52435400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:52435400-52435600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:52435600-52435800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:52436800-52437200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr2:52436800-52438600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr2:52437400-52438000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr2:52442000-52443800	Enhancers	Fetal Heart	heart
24	chr2:52443800-52448600	Weak transcription	Fetal Heart	heart
25	chr2:52448600-52449800	Enhancers	Fetal Heart	heart
26	chr2:52449400-52449800	Enhancers	NHDF-Ad	bronchial
27	chr2:52449600-52450000	Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr2:52451600-52452600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:52452600-52454600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:52454600-52455200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:52463200-52464000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:52463400-52463800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:52463400-52463800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr2:52463800-52464000	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr2:52463800-52464600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr2:52463800-52466000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr2:52464000-52464400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr2:52464400-52465000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr2:52464600-52464800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:52464800-52465800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr2:52465000-52466200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr2:52465800-52466000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:52465800-52466400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr2:52465800-52466400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:52466000-52466200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr2:52466000-52466400	Enhancers	H9 Cell Line	embryonic stem cell
47	chr2:52466000-52466400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr2:52466000-52466400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr2:52466200-52466400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:52479400-52479600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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