Variant report

Variant	nsv431047
Chromosome Location	chr2:51961737-52263543
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:985)
CpG islands
(count:429)
Chromatin interactive
region (count:43)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:985 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:51985283-51985521	HepG2	liver:	n/a	n/a
2	BACH1	chr2:52185802-52185829	K562	blood:	n/a	n/a
3	BACH1	chr2:52208991-52209296	H1-hESC	embryonic stem cell:	n/a	chr2:52209155-52209169
4	BACH1	chr2:52013621-52013717	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:52196504-52196856	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:52196504-52196867	K562	blood:	n/a	n/a
7	BRCA1	chr2:52259388-52259484	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr2:52040441-52040852	HCT-116	colon:	n/a	n/a
9	CEBPB	chr2:52020207-52020467	IMR90	lung:	n/a	chr2:52020327-52020338 chr2:52020277-52020288
10	CEBPB	chr2:52010523-52010856	IMR90	lung:	n/a	chr2:52010684-52010695
11	CEBPB	chr2:52222380-52222693	A549	lung:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
12	CEBPB	chr2:52130909-52131253	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr2:52106555-52106796	HepG2	liver:	n/a	chr2:52106702-52106713
14	CEBPB	chr2:52130863-52131276	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr2:52104076-52104488	HCT-116	colon:	n/a	n/a
16	CEBPB	chr2:52107350-52107669	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:52130882-52131188	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:52010516-52010845	A549	lung:	n/a	chr2:52010684-52010695
19	CEBPB	chr2:52227686-52227965	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:52117644-52117838	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:52051683-52051729	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr2:52051511-52051735	A549	lung:	n/a	n/a
23	CEBPB	chr2:52040436-52040772	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:52010535-52010824	HepG2	liver:	n/a	chr2:52010684-52010695
25	CEBPB	chr2:52203479-52204403	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:52193961-52194229	Hela-S3	cervix:	n/a	chr2:52194121-52194132
27	CEBPB	chr2:52133005-52133191	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr2:52146526-52146921	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:52130905-52131200	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:52052956-52053358	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:52057437-52057715	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:52194008-52194207	A549	lung:	n/a	chr2:52194121-52194132
33	CEBPB	chr2:52118783-52118811	HepG2	liver:	n/a	chr2:52118792-52118803
34	CEBPB	chr2:52222385-52222704	HepG2	liver:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
35	CEBPB	chr2:52093449-52093880	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:52130970-52131211	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:52222367-52222678	H1-hESC	embryonic stem cell:	n/a	chr2:52222524-52222537 chr2:52222524-52222535
38	CEBPB	chr2:52130908-52131192	K562	blood:	n/a	n/a
39	CEBPB	chr2:52168493-52168547	A549	lung:	n/a	n/a
40	CEBPB	chr2:52126935-52126947	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:52181882-52182126	IMR90	lung:	n/a	n/a
42	CEBPB	chr2:52020231-52020456	A549	lung:	n/a	chr2:52020327-52020338 chr2:52020277-52020288
43	CEBPB	chr2:51991752-51992063	HepG2	liver:	n/a	chr2:51991926-51991937
44	CEBPB	chr2:51991789-51992037	IMR90	lung:	n/a	chr2:51991926-51991937
45	CEBPB	chr2:52170578-52170756	HepG2	liver:	n/a	chr2:52170622-52170633
46	CEBPB	chr2:52215321-52215434	HepG2	liver:	n/a	n/a
47	CEBPB	chr2:52193973-52194288	IMR90	lung:	n/a	chr2:52194121-52194132
48	CEBPB	chr2:52257247-52257351	A549	lung:	n/a	n/a
49	CEBPB	chr2:51991600-51992080	Hela-S3	cervix:	n/a	chr2:51991926-51991937
50	CEBPB	chr2:52215249-52215477	A549	lung:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52039654-52039704	AG09309	skin:	n/a
2	chr2:52039654-52039704	NT2-D1	testis:	n/a
3	chr2:52039654-52039704	AG09309	skin:	n/a
4	chr2:52039654-52039704	NT2-D1	testis:	n/a
5	chr2:52234104-52234154	HIPEpiC	eye:	n/a
6	chr2:52235062-52235112	AG04450	lung:	fetal
7	chr2:52007665-52007715	GM12892	blood:	n/a
8	chr2:52235062-52235112	GM12892	blood:	n/a
9	chr2:52235062-52235112	ProgFib	skin:	n/a
10	chr2:52006728-52006778	MCF-7	breast:	n/a
11	chr2:52006728-52006778	NHBE	bronchial:	n/a
12	chr2:52234104-52234154	NT2-D1	testis:	n/a
13	chr2:52039654-52039704	PrEC	prostate:	n/a
14	chr2:52221668-52221718	SKMC	muscle:	n/a
15	chr2:52007582-52007632	SK-N-SH	brain:	n/a
16	chr2:52234104-52234154	HEK293	kidney:	embryo
17	chr2:52235062-52235112	AoSMC	blood vessel:	n/a
18	chr2:52007665-52007715	NB4	blood:	n/a
19	chr2:52234104-52234154	GM12878	blood:	n/a
20	chr2:52221668-52221718	NB4	blood:	n/a
21	chr2:52234104-52234154	K562	blood:	n/a
22	chr2:52039654-52039704	RPTEC	kidney:	n/a
23	chr2:52221668-52221718	AG10803	skin:	n/a
24	chr2:52235062-52235112	AG10803	skin:	n/a
25	chr2:52235062-52235112	Hela-S3	cervix:	n/a
26	chr2:52039654-52039704	NHDF-neo	bronchial:	n/a
27	chr2:52006728-52006778	HL-60	blood:	n/a
28	chr2:52006728-52006778	HUVEC	blood vessel:	n/a
29	chr2:52039654-52039704	HUVEC	blood vessel:	n/a
30	chr2:52006728-52006778	NB4	blood:	n/a
31	chr2:52235062-52235112	H1-hESC	embryonic stem cell:	embryo
32	chr2:52234104-52234154	HRCEpiC	kidney:	n/a
33	chr2:52235062-52235112	HRCEpiC	kidney:	n/a
34	chr2:52235062-52235112	SK-N-MC	brain:	n/a
35	chr2:52007582-52007632	HNPCEpiC	eye:	n/a
36	chr2:52007582-52007632	HCT-116	colon:	n/a
37	chr2:52039654-52039704	Hela-S3	cervix:	n/a
38	chr2:52221668-52221718	ECC-1	luminal epithelium:	n/a
39	chr2:52235062-52235112	MCF10A-Er-Src	breast:	n/a
40	chr2:52221668-52221718	HCM	heart:	n/a
41	chr2:52235062-52235112	NHBE	bronchial:	n/a
42	chr2:52007582-52007632	PANC-1	pancreas:	n/a
43	chr2:52007665-52007715	PANC-1	pancreas:	n/a
44	chr2:52006728-52006778	SKMC	muscle:	n/a
45	chr2:52234104-52234154	PFSK-1	brain:	n/a
46	chr2:52006728-52006778	HRPEpiC	eye:	n/a
47	chr2:52039654-52039704	AG10803	skin:	n/a
48	chr2:52234104-52234154	NHBE	bronchial:	n/a
49	chr2:52007582-52007632	SKMC	muscle:	n/a
50	chr2:52039654-52039704	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:52069239..52070064-chr8:36656303..36657160,2	MCF-7	breast:
2	chr2:51969395..51971476-chr2:51980845..51983747,2	K562	blood:
3	2:51664217-51674289..2:51974300-51979334	H1-hESC	embryonic stem cell:	embryo
4	chr2:50763606..50764181-chr2:52224822..52225393,2	MCF-7	breast:
5	2:52043909-52049825..2:52049825-52050373	K562	blood:
6	chr2:52261393..52263430-chr2:52272675..52274372,2	K562	blood:
7	2:52132828-52140118..2:52144960-52145427	GM12878	blood:
8	chr2:52097711..52099315-chr2:52104533..52106401,2	K562	blood:
9	2:51681598-51686731..2:51983874-51990011	GM12878	blood:
10	chr2:52013693..52015857-chr2:52040010..52042547,2	K562	blood:
11	2:51675236-51679533..2:52132828-52140118	GM12878	blood:
12	chr2:52002782..52005199-chr2:52008928..52011159,2	K562	blood:
13	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
14	2:52132828-52140118..2:52144960-52145427	GM12878	blood:
15	2:51664217-51674289..2:52006946-52008886	H1-hESC	embryonic stem cell:	embryo
16	chr2:52002782..52005199-chr2:52008928..52011159,2	K562	blood:
17	2:51664217-51674289..2:52132828-52140118	H1-hESC	embryonic stem cell:	embryo
18	2:51755125-51764739..2:52034460-52043624	K562	blood:
19	chr2:52045177..52047183-chr2:52049220..52051220,2	K562	blood:
20	chr2:52013693..52015857-chr2:52040010..52042547,2	K562	blood:
21	chr2:51968237..51969919-chr2:51972902..51975746,2	K562	blood:
22	chr11:63952383..63953021-chr2:52077502..52078002,2	Hela-S3	cervix:
23	chr2:51969395..51971476-chr2:51980845..51983747,2	K562	blood:
24	2:51785137-51786126..2:52106672-52112664	GM12878	blood:
25	chr2:52045177..52047313-chr2:52049220..52051486,2	K562	blood:
26	chr2:52239790..52242380-chr2:52244407..52246519,2	K562	blood:
27	chr2:52239790..52242380-chr2:52244407..52246519,2	K562	blood:
28	chr2:52063384..52066305-chr2:52068038..52070794,3	K562	blood:
29	2:51664217-51674289..2:52112664-52117037	K562	blood:
30	2:51664217-51674289..2:52043909-52049825	H1-hESC	embryonic stem cell:	embryo
31	2:51745267-51754233..2:52043624-52043909	K562	blood:
32	chr2:51968237..51969919-chr2:51972902..51975746,2	K562	blood:
33	2:51664217-51674289..2:51983874-51990011	GM12878	blood:
34	2:51664217-51674289..2:52034460-52043624	GM12878	blood:
35	chr2:50756714..50757394-chr2:52022672..52023233,2	MCF-7	breast:
36	2:51664217-51674289..2:52100874-52104046	H1-hESC	embryonic stem cell:	embryo
37	chr2:52097711..52099315-chr2:52104533..52106401,2	K562	blood:
38	2:51664217-51674289..2:52055539-52058793	H1-hESC	embryonic stem cell:	embryo
39	chr2:52045177..52047313-chr2:52049220..52051486,2	K562	blood:
40	chr2:52045177..52047183-chr2:52049220..52051220,2	K562	blood:
41	2:51745267-51754233..2:52106672-52112664	GM12878	blood:
42	chr2:52063384..52066305-chr2:52068038..52070794,3	K562	blood:
43	2:52043909-52049825..2:52049825-52050373	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-4	chr2:52088587-52088626	ENSG00000231918.1
2	lnc-CHAC2-4	chr2:51989227-51989312	ENSG00000231918.1

No data

Variant related genes	Relation type
CRYGGP	TF binding region
ENSG00000226366	TF binding region
ENSG00000230840	TF binding region
CRYGGP	CpG island
ENSG00000226366	CpG island
ENSG00000230840	CpG island
ENSG00000168439	chromatin interactions

Extended variants
information (count: 6064 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:6064 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545768508	chr2:51984404-51984405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535959787	chr2:51984408-51984409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141737116	chr2:51984451-51984452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78102925	chr2:51984458-51984459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17863691	chr2:51984459-51984460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546535638	chr2:51984495-51984496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11563113	chr2:51984518-51984519	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs192278733	chr2:51984519-51984520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148054710	chr2:51984535-51984536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112562050	chr2:51984571-51984572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568913638	chr2:51984591-51984592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534424218	chr2:51984643-51984644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557779430	chr2:51984659-51984660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566522158	chr2:51984741-51984742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182886674	chr2:51984755-51984756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554206483	chr2:51984785-51984786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17868236	chr2:51984788-51984789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs28965172	chr2:51984809-51984810	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs34287517	chr2:51984834-51984835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548533916	chr2:51984845-51984846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73930761	chr2:51984873-51984874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372260423	chr2:51984884-51984885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs76592305	chr2:51984889-51984890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567261938	chr2:51984975-51984976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs193116928	chr2:51985022-51985023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537495787	chr2:51985179-51985180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564135399	chr2:51985182-51985183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371481932	chr2:51985199-51985200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557850120	chr2:51985212-51985213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11418028	chr2:51985213-51985214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528422394	chr2:51985218-51985219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150619089	chr2:51985230-51985231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367546093	chr2:51985237-51985238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76082681	chr2:51985241-51985242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371860228	chr2:51985258-51985259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563275550	chr2:51985263-51985264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568999382	chr2:51985269-51985270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576715906	chr2:51985275-51985276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11563265	chr2:51985286-51985287	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs551451352	chr2:51985306-51985307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139676629	chr2:51985316-51985317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533732309	chr2:51985344-51985345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369143465	chr2:51985378-51985379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187699129	chr2:51985392-51985393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116770505	chr2:51985422-51985423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535805741	chr2:51985423-51985424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144723401	chr2:51985446-51985447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575478552	chr2:51985448-51985449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559490617	chr2:51985454-51985455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11563085	chr2:51985455-51985456	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51984400-51985800	Enhancers	Hela-S3	cervix
2	chr2:51986600-51987200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:51987200-51987800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:51987800-51988000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr2:51999600-52001800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:52001800-52002200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:52005600-52007000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:52005600-52007000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:52005800-52006800	ZNF genes & repeats	HepG2	liver
10	chr2:52006000-52006400	Enhancers	Fetal Muscle Leg	muscle
11	chr2:52006000-52006400	Active TSS	Osteobl	bone
12	chr2:52006800-52008000	Weak transcription	HepG2	liver
13	chr2:52006800-52011000	Weak transcription	Right Atrium	heart
14	chr2:52007000-52009400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:52008000-52008400	ZNF genes & repeats	HepG2	liver
16	chr2:52008800-52009400	Enhancers	Fetal Brain Male	brain
17	chr2:52009000-52012000	Enhancers	Fetal Heart	heart
18	chr2:52009400-52009800	Weak transcription	Fetal Brain Male	brain
19	chr2:52009400-52009800	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr2:52009400-52010800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:52009800-52010200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr2:52009800-52011400	Enhancers	Fetal Brain Male	brain
23	chr2:52010000-52010400	Enhancers	Fetal Brain Female	brain
24	chr2:52010000-52010600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:52010000-52010600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:52010000-52010600	Enhancers	HMEC	breast
27	chr2:52010200-52010600	Enhancers	NHDF-Ad	bronchial
28	chr2:52010200-52010800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr2:52010200-52010800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr2:52010200-52011000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr2:52011000-52011600	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr2:52011600-52011800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr2:52016800-52018000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:52017000-52017400	Enhancers	Osteobl	bone
35	chr2:52017000-52017600	Enhancers	Adipose Nuclei	Adipose
36	chr2:52018000-52019000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:52019000-52019200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:52022000-52022400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:52022000-52022600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:52022000-52022800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:52022200-52022600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr2:52022400-52022800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr2:52022400-52023000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:52032400-52032800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:52032400-52032800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
46	chr2:52032800-52035200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:52035200-52035400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr2:52037200-52037600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr2:52037600-52038400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr2:52038200-52039200	Enhancers	Hela-S3	cervix

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