Variant report

Variant	nsv1014342
Chromosome Location	chr2:52114176-52378299
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	BACH1	chr2:52362389-52362723	K562	blood:	n/a	n/a
2	BACH1	chr2:52208991-52209296	H1-hESC	embryonic stem cell:	n/a	chr2:52209155-52209169
3	BACH1	chr2:52196504-52196856	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:52362395-52362744	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:52196504-52196867	K562	blood:	n/a	n/a
6	BACH1	chr2:52185802-52185829	K562	blood:	n/a	n/a
7	BATF	chr2:52304385-52304596	GM12878	blood:	n/a	n/a
8	BRCA1	chr2:52259388-52259484	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr2:52310166-52311117	HCT-116	colon:	n/a	n/a
10	CBX3	chr2:52309795-52311146	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:52263141-52263506	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:52257247-52257351	A549	lung:	n/a	n/a
13	CEBPB	chr2:52324251-52324554	ECC-1	luminal epithelium:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
14	CEBPB	chr2:52324213-52324590	Hela-S3	cervix:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
15	CEBPB	chr2:52284303-52284564	A549	lung:	n/a	chr2:52284412-52284421 chr2:52284412-52284423 chr2:52284410-52284423 chr2:52284410-52284421
16	CEBPB	chr2:52317588-52317783	IMR90	lung:	n/a	chr2:52317668-52317679
17	CEBPB	chr2:52193951-52194247	HepG2	liver:	n/a	chr2:52194121-52194132
18	CEBPB	chr2:52323284-52323495	A549	lung:	n/a	chr2:52323383-52323394 chr2:52323383-52323396 chr2:52323383-52323396
19	CEBPB	chr2:52222480-52222649	K562	blood:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
20	CEBPB	chr2:52309821-52310890	HCT-116	colon:	n/a	n/a
21	CEBPB	chr2:52344406-52344788	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:52130863-52131276	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr2:52168493-52168547	A549	lung:	n/a	n/a
24	CEBPB	chr2:52193961-52194229	Hela-S3	cervix:	n/a	chr2:52194121-52194132
25	CEBPB	chr2:52117644-52117838	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:52222367-52222678	H1-hESC	embryonic stem cell:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
27	CEBPB	chr2:52222401-52222715	Hela-S3	cervix:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
28	CEBPB	chr2:52130917-52131217	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr2:52126935-52126947	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:52324229-52324587	HepG2	liver:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
31	CEBPB	chr2:52170497-52170767	IMR90	lung:	n/a	chr2:52170622-52170633
32	CEBPB	chr2:52324253-52324595	H1-hESC	embryonic stem cell:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
33	CEBPB	chr2:52203479-52204403	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:52222385-52222704	HepG2	liver:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
35	CEBPB	chr2:52231382-52231629	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:52324255-52324571	A549	lung:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
37	CEBPB	chr2:52133005-52133191	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:52344349-52344906	HCT-116	colon:	n/a	n/a
39	CEBPB	chr2:52344262-52344853	HCT-116	colon:	n/a	n/a
40	CEBPB	chr2:52362409-52362746	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:52231435-52231623	A549	lung:	n/a	n/a
42	CEBPB	chr2:52146418-52146943	Hela-S3	cervix:	n/a	chr2:52146442-52146455
43	CEBPB	chr2:52194035-52194142	H1-hESC	embryonic stem cell:	n/a	chr2:52194121-52194132
44	CEBPB	chr2:52194008-52194207	A549	lung:	n/a	chr2:52194121-52194132
45	CEBPB	chr2:52324312-52324599	MCF-7	breast:	n/a	chr2:52324407-52324416 chr2:52324407-52324416 chr2:52324407-52324416
46	CEBPB	chr2:52130908-52131192	K562	blood:	n/a	n/a
47	CEBPB	chr2:52130909-52131253	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr2:52118783-52118811	HepG2	liver:	n/a	chr2:52118792-52118803
49	CEBPB	chr2:52282155-52282341	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr2:52344400-52344790	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52221668-52221718	SK-N-MC	brain:	n/a
2	chr2:52272404-52272454	SK-N-SH	brain:	n/a
3	chr2:52221668-52221718	GM12878	blood:	n/a
4	chr2:52235062-52235112	Hepatocyte	liver:	n/a
5	chr2:52281777-52281827	ProgFib	skin:	n/a
6	chr2:52281777-52281827	HRCEpiC	kidney:	n/a
7	chr2:52234104-52234154	Caco-2	colon:	n/a
8	chr2:52235062-52235112	HepG2	liver:	n/a
9	chr2:52235062-52235112	SK-N-SH	brain:	n/a
10	chr2:52272404-52272454	SK-N-SH_RA	brain:	n/a
11	chr2:52272404-52272454	T-47D	breast:	n/a
12	chr2:52281777-52281827	ovcar-3	ovarian:	n/a
13	chr2:52281777-52281827	SK-N-SH_RA	brain:	n/a
14	chr2:52235062-52235112	CMK	blood:	n/a
15	chr2:52281777-52281827	SKMC	muscle:	n/a
16	chr2:52272404-52272454	HCM	heart:	n/a
17	chr2:52235062-52235112	AG09319	gingival:	n/a
18	chr2:52235062-52235112	HNPCEpiC	eye:	n/a
19	chr2:52281777-52281827	HUVEC	blood vessel:	n/a
20	chr2:52281777-52281827	SAEC	small airway:	n/a
21	chr2:52281777-52281827	HCT-116	colon:	n/a
22	chr2:52235062-52235112	SKMC	muscle:	n/a
23	chr2:52272404-52272454	PANC-1	pancreas:	n/a
24	chr2:52235062-52235112	A549	lung:	n/a
25	chr2:52234104-52234154	AG10803	skin:	n/a
26	chr2:52272404-52272454	HCPEpiC	choroid plexus:	n/a
27	chr2:52235062-52235112	ProgFib	skin:	n/a
28	chr2:52272404-52272454	PrEC	prostate:	n/a
29	chr2:52235062-52235112	NT2-D1	testis:	n/a
30	chr2:52281777-52281827	HRPEpiC	eye:	n/a
31	chr2:52234104-52234154	GM19239	blood:	n/a
32	chr2:52235062-52235112	HMEC	breast:	n/a
33	chr2:52221668-52221718	SAEC	small airway:	n/a
34	chr2:52221668-52221718	IMR90	lung:	fetal
35	chr2:52272404-52272454	ProgFib	skin:	n/a
36	chr2:52272404-52272454	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:52221668-52221718	Caco-2	colon:	n/a
38	chr2:52235062-52235112	GM12891	blood:	n/a
39	chr2:52234104-52234154	CMK	blood:	n/a
40	chr2:52281777-52281827	RPTEC	kidney:	n/a
41	chr2:52281777-52281827	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:52234104-52234154	NT2-D1	testis:	n/a
43	chr2:52235062-52235112	PFSK-1	brain:	n/a
44	chr2:52234104-52234154	T-47D	breast:	n/a
45	chr2:52221668-52221718	HRE	kidney:	n/a
46	chr2:52221668-52221718	GM12891	blood:	n/a
47	chr2:52272404-52272454	Jurkat	blood:	n/a
48	chr2:52272404-52272454	Hepatocyte	liver:	n/a
49	chr2:52272404-52272454	HRPEpiC	eye:	n/a
50	chr2:52234104-52234154	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:50763606..50764181-chr2:52224822..52225393,2	MCF-7	breast:
2	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
3	2:51664217-51674289..2:52132828-52140118	H1-hESC	embryonic stem cell:	embryo
4	chr2:52344101..52346354-chr2:52360940..52363061,2	MCF-7	breast:
5	chr2:52261393..52263430-chr2:52272675..52274372,2	K562	blood:
6	chr2:52367783..52370728-chr2:52370744..52372935,2	K562	blood:
7	chr2:52321532..52323280-chr2:52325089..52327796,2	K562	blood:
8	chr2:52335533..52337278-chr2:52346386..52348387,2	K562	blood:
9	chr2:52239790..52242380-chr2:52244407..52246519,2	K562	blood:
10	chr2:52344101..52346354-chr2:52360940..52363061,2	MCF-7	breast:
11	2:51675236-51679533..2:52132828-52140118	GM12878	blood:
12	chr2:52367783..52370728-chr2:52370744..52372935,2	K562	blood:
13	2:51664217-51674289..2:52112664-52117037	K562	blood:
14	2:52132828-52140118..2:52144960-52145427	GM12878	blood:
15	chr2:52335533..52337278-chr2:52346386..52348387,2	K562	blood:
16	chr2:52261393..52263430-chr2:52272675..52274372,2	K562	blood:
17	chr2:52357469..52360071-chr20:52739539..52742222,2	MCF-7	breast:
18	chr2:52321532..52323280-chr2:52325089..52327796,2	K562	blood:
19	chr2:52239790..52242380-chr2:52244407..52246519,2	K562	blood:
20	2:52132828-52140118..2:52144960-52145427	GM12878	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-11	chr2:52298493-52298559	NONHSAT070666
2	lnc-CHAC2-11	chr2:52302622-52302775	NONHSAT070666
3	lnc-CHAC2-11	chr2:52304140-52304335	NONHSAT070666

Variant related genes	Relation type
ENSG00000226366	TF binding region
ZNF863P	TF binding region
ENSG00000230840	TF binding region
ENSG00000226366	CpG island
ZNF863P	CpG island
ENSG00000230840	CpG island

Extended variants
information (count: 5391 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:5391 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs984093	chr2:52114176-52114177	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570725195	chr2:52115411-52115412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80135847	chr2:52115426-52115427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553332598	chr2:52115450-52115451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141102816	chr2:52115477-52115478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191645080	chr2:52115480-52115481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556831010	chr2:52115548-52115549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575318847	chr2:52115579-52115580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184113870	chr2:52115580-52115581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545545310	chr2:52115596-52115597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188072753	chr2:52115597-52115598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572531474	chr2:52115632-52115633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568439647	chr2:52115635-52115636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539835893	chr2:52115638-52115639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559658917	chr2:52115650-52115651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530287530	chr2:52115750-52115751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376758195	chr2:52115754-52115755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548769059	chr2:52115783-52115784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530842325	chr2:52115787-52115788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563704504	chr2:52115831-52115832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531052312	chr2:52115858-52115859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113576158	chr2:52115878-52115879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7567448	chr2:52115881-52115882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs372453081	chr2:52115887-52115888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557463616	chr2:52115898-52115899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112829642	chr2:52115906-52115907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111580074	chr2:52115914-52115915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535066439	chr2:52115975-52115976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573975747	chr2:52115996-52115997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112455157	chr2:52116087-52116088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547008178	chr2:52116102-52116103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568373572	chr2:52116106-52116107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs67733645	chr2:52116119-52116120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557133602	chr2:52116135-52116136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113962802	chr2:52116161-52116162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539609469	chr2:52116164-52116165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376317198	chr2:52116174-52116175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs17868284	chr2:52116200-52116201	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs192409684	chr2:52116225-52116226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572590906	chr2:52116228-52116229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539849964	chr2:52116287-52116288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554899233	chr2:52116322-52116323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567939755	chr2:52116338-52116339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574816715	chr2:52116386-52116387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542126537	chr2:52116416-52116417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138173070	chr2:52116430-52116431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs202092478	chr2:52116431-52116432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79862125	chr2:52116432-52116433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563995635	chr2:52116492-52116493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138030772	chr2:52116530-52116531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52112800-52114200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr2:52115400-52115800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:52115600-52115800	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:52115800-52129400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:52116000-52116800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr2:52116800-52117200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:52127000-52127400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr2:52136000-52136400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:52136000-52136600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:52144600-52145600	Enhancers	NHDF-Ad	bronchial
11	chr2:52144600-52147800	Enhancers	Osteobl	bone
12	chr2:52144800-52146400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:52144800-52146600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr2:52144800-52147400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:52144800-52147600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr2:52144800-52148000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:52145000-52145600	Enhancers	Adipose Nuclei	Adipose
18	chr2:52145400-52146600	Enhancers	HMEC	breast
19	chr2:52145600-52146200	Weak transcription	NHDF-Ad	bronchial
20	chr2:52146200-52147200	Enhancers	NHDF-Ad	bronchial
21	chr2:52146400-52146600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:52146400-52148200	Enhancers	Hela-S3	cervix
23	chr2:52146600-52147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:52147000-52147400	Enhancers	NHLF	lung
25	chr2:52147600-52147800	Enhancers	Adipose Nuclei	Adipose
26	chr2:52147600-52148200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:52147800-52151400	Weak transcription	Osteobl	bone
28	chr2:52151400-52151600	ZNF genes & repeats	Osteobl	bone
29	chr2:52166000-52166400	ZNF genes & repeats	Primary T cells from cord blood	blood
30	chr2:52170800-52171200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:52171200-52178800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:52175400-52175600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr2:52175600-52176200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:52178200-52178400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr2:52178800-52179800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:52180600-52180800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr2:52180600-52182000	Enhancers	NHDF-Ad	bronchial
38	chr2:52180800-52181200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr2:52180800-52181600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:52180800-52182400	Enhancers	Osteobl	bone
41	chr2:52181200-52182200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr2:52181600-52182000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr2:52182000-52182200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr2:52182000-52186400	Weak transcription	NHDF-Ad	bronchial
45	chr2:52182200-52182600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:52182600-52186200	Weak transcription	Osteobl	bone
47	chr2:52186200-52188400	Enhancers	Osteobl	bone
48	chr2:52186400-52186600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr2:52186400-52188400	Enhancers	NHDF-Ad	bronchial
50	chr2:52186600-52187200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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