Variant report

Variant	nsv818057
Chromosome Location	chr2:78263883-78633880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:713)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:78413821-78414186	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:78336522-78336700	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:78361077-78361118	K562	blood:	n/a	n/a
4	ARID3A	chr2:78389314-78389802	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:78578413-78578720	K562	blood:	n/a	n/a
6	ARID3A	chr2:78578391-78578636	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:78487915-78488675	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:78532952-78532953	K562	blood:	n/a	n/a
9	ATF1	chr2:78361002-78361126	K562	blood:	n/a	n/a
10	ATF1	chr2:78408127-78408325	K562	blood:	n/a	n/a
11	BACH1	chr2:78477710-78477711	K562	blood:	n/a	n/a
12	BACH1	chr2:78368178-78368199	K562	blood:	n/a	n/a
13	BATF	chr2:78508306-78508624	GM12878	blood:	n/a	n/a
14	BATF	chr2:78508305-78508535	GM12878	blood:	n/a	n/a
15	BATF	chr2:78428253-78428380	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:78508311-78508495	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:78389461-78389669	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:78490807-78490864	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:78508455-78508636	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:78487986-78488343	HepG2	liver:	n/a	n/a
21	CBX3	chr2:78273156-78273427	K562	blood:	n/a	n/a
22	CBX3	chr2:78273160-78273446	K562	blood:	n/a	n/a
23	CEBPB	chr2:78335197-78335393	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:78278617-78278979	IMR90	lung:	n/a	chr2:78278787-78278798
25	CEBPB	chr2:78420652-78420781	K562	blood:	n/a	n/a
26	CEBPB	chr2:78420675-78420797	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:78278610-78278979	HepG2	liver:	n/a	chr2:78278787-78278798
28	CEBPB	chr2:78275936-78276189	HepG2	liver:	n/a	chr2:78276047-78276058
29	CEBPB	chr2:78589456-78589783	HepG2	liver:	n/a	chr2:78589637-78589648
30	CEBPB	chr2:78278654-78278947	K562	blood:	n/a	chr2:78278787-78278798
31	CEBPB	chr2:78518559-78518875	IMR90	lung:	n/a	chr2:78518707-78518718
32	CEBPB	chr2:78389473-78389661	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:78589457-78589745	A549	lung:	n/a	chr2:78589637-78589648
34	CEBPB	chr2:78376053-78376336	HepG2	liver:	n/a	chr2:78376191-78376202
35	CEBPB	chr2:78278630-78278975	A549	lung:	n/a	chr2:78278787-78278798
36	CEBPB	chr2:78336403-78336930	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:78336515-78336886	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr2:78606574-78606774	A549	lung:	n/a	n/a
39	CEBPB	chr2:78336445-78336815	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:78288591-78288834	HepG2	liver:	n/a	chr2:78288709-78288720
41	CEBPB	chr2:78583349-78583384	K562	blood:	n/a	n/a
42	CEBPB	chr2:78589546-78589687	H1-hESC	embryonic stem cell:	n/a	chr2:78589637-78589648
43	CEBPB	chr2:78369163-78369459	HepG2	liver:	n/a	chr2:78369346-78369359 chr2:78369367-78369378
44	CEBPB	chr2:78359289-78359640	MCF-7	breast:	n/a	n/a
45	CEBPB	chr2:78590365-78590520	A549	lung:	n/a	n/a
46	CEBPB	chr2:78275962-78276210	IMR90	lung:	n/a	chr2:78276047-78276058
47	CEBPB	chr2:78518569-78518898	K562	blood:	n/a	chr2:78518707-78518718
48	CEBPB	chr2:78336457-78336666	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:78420619-78420902	HepG2	liver:	n/a	n/a
50	CEBPB	chr2:78577077-78577375	IMR90	lung:	n/a	chr2:78577256-78577265 chr2:78577254-78577265 chr2:78577256-78577267 chr2:78577256-78577265 chr2:78577256-78577265 chr2:78577256-78577265

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:78545567-78545617	SK-N-MC	brain:	n/a
2	chr2:78545567-78545617	HCF	heart:	n/a
3	chr2:78545567-78545617	NH-A	brain:	n/a
4	chr2:78545567-78545617	SAEC	small airway:	n/a
5	chr2:78545567-78545617	BE2_C	brain:	n/a
6	chr2:78545567-78545617	HRCEpiC	kidney:	n/a
7	chr2:78545567-78545617	CMK	blood:	n/a
8	chr2:78545567-78545617	AG04450	lung:	fetal
9	chr2:78545567-78545617	PFSK-1	brain:	n/a
10	chr2:78545567-78545617	GM12892	blood:	n/a
11	chr2:78545567-78545617	HIPEpiC	eye:	n/a
12	chr2:78545567-78545617	GM12891	blood:	n/a
13	chr2:78545567-78545617	Hela-S3	cervix:	n/a
14	chr2:78545567-78545617	PrEC	prostate:	n/a
15	chr2:78545567-78545617	HEEpiC	esophagus:	n/a
16	chr2:78545567-78545617	ECC-1	luminal epithelium:	n/a
17	chr2:78545567-78545617	NHBE	bronchial:	n/a
18	chr2:78545567-78545617	H1-hESC	embryonic stem cell:	embryo
19	chr2:78545567-78545617	BJ	skin:	n/a
20	chr2:78545567-78545617	HCM	heart:	n/a
21	chr2:78545567-78545617	HRPEpiC	eye:	n/a
22	chr2:78545567-78545617	NB4	blood:	n/a
23	chr2:78545567-78545617	GM06990	blood:	n/a
24	chr2:78545567-78545617	HRE	kidney:	n/a
25	chr2:78545567-78545617	HEK293	kidney:	embryo
26	chr2:78545567-78545617	HepG2	liver:	n/a
27	chr2:78545567-78545617	AG09319	gingival:	n/a
28	chr2:78545567-78545617	AG09309	skin:	n/a
29	chr2:78545567-78545617	HCPEpiC	choroid plexus:	n/a
30	chr2:78545567-78545617	GM12878	blood:	n/a
31	chr2:78545567-78545617	AoSMC	blood vessel:	n/a
32	chr2:78545567-78545617	Caco-2	colon:	n/a
33	chr2:78545567-78545617	HL-60	blood:	n/a
34	chr2:78545567-78545617	HCT-116	colon:	n/a
35	chr2:78545567-78545617	NT2-D1	testis:	n/a
36	chr2:78545567-78545617	MCF-7	breast:	n/a
37	chr2:78545567-78545617	ovcar-3	ovarian:	n/a
38	chr2:78545567-78545617	HAEpiC	amniotic membrane:	n/a
39	chr2:78545567-78545617	MCF10A-Er-Src	breast:	n/a
40	chr2:78545567-78545617	SK-N-SH	brain:	n/a
41	chr2:78545567-78545617	K562	blood:	n/a
42	chr2:78545567-78545617	U87	brain:	n/a
43	chr2:78545567-78545617	Jurkat	blood:	n/a
44	chr2:78545567-78545617	IMR90	lung:	fetal
45	chr2:78545567-78545617	HNPCEpiC	eye:	n/a
46	chr2:78545567-78545617	SK-N-SH_RA	brain:	n/a
47	chr2:78545567-78545617	HMEC	breast:	n/a
48	chr2:78545567-78545617	HUVEC	blood vessel:	n/a
49	chr2:78545567-78545617	GM19239	blood:	n/a
50	chr2:78545567-78545617	RPTEC	kidney:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
2	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
3	chr2:78519747..78522682-chr2:78785137..78786876,2	K562	blood:
4	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
5	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
6	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
7	chr2:78577613..78578539-chr2:79206466..79207847,3	MCF-7	breast:
8	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
9	chr2:78347733..78349406-chr2:78351881..78353903,2	K562	blood:
10	chr2:78295743..78297764-chr2:78300068..78303067,2	K562	blood:
11	chr2:78607954..78609567-chr2:78764622..78766807,2	K562	blood:
12	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
13	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
14	chr17:59624355..59624932-chr2:78345304..78345966,2	MCF-7	breast:
15	chr2:78578903..78584135-chr2:78585848..78590226,6	K562	blood:
16	chr2:78552005..78554249-chr2:78556086..78558009,2	K562	blood:
17	chr2:78538765..78541253-chr2:78550718..78553114,2	K562	blood:
18	chr2:78578454..78579130-chr2:79226516..79227199,2	MCF-7	breast:
19	chr2:78326493..78328202-chr2:78333273..78335963,2	K562	blood:
20	chr2:78577011..78577791-chr8:96157456..96158424,2	MCF-7	breast:
21	chr2:78347906..78350697-chr2:78350756..78353381,2	K562	blood:
22	chr2:78300847..78302731-chr2:78308537..78310502,2	K562	blood:
23	chr2:78578299..78578916-chr2:79206809..79207351,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRTM4-8	chr2:78371022-78371323	ucscGeneNc_uc002snu_2
2	lnc-REG3G-3	chr2:78354625-78354877	XLOC_001543
3	lnc-REG3G-3	chr2:78322790-78322968	XLOC_001543
4	lnc-REG3G-3	chr2:78320703-78320792	XLOC_001543
5	lnc-REG3G-3	chr2:78321763-78321902	XLOC_001543
6	lnc-LRRTM4-3	chr2:78517514-78517857	NR_110288
7	lnc-REG3G-3	chr2:78339185-78339226	XLOC_001543

No data

Variant related genes	Relation type
ENSG00000229494	TF binding region
ENSG00000229494	CpG island

Extended variants
information (count: 5930 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5930 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1527194	chr2:78263883-78263884	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12713939	chr2:78263967-78263968	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs147027813	chr2:78264010-78264011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556593157	chr2:78264064-78264065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs5832314	chr2:78264065-78264066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75603571	chr2:78264066-78264067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76922148	chr2:78264077-78264078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs5019111	chr2:78264113-78264114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs574537937	chr2:78264143-78264144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185841357	chr2:78264189-78264190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369266979	chr2:78264235-78264236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113016527	chr2:78264284-78264285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191075586	chr2:78264332-78264333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116837505	chr2:78264354-78264355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182012046	chr2:78264365-78264366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2141122	chr2:78264378-78264379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs543674052	chr2:78264414-78264415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562207376	chr2:78264439-78264440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531312270	chr2:78264440-78264441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2141121	chr2:78264462-78264463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs369919766	chr2:78264491-78264492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564532796	chr2:78264523-78264524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150508191	chr2:78264535-78264536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10175874	chr2:78264577-78264578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561049079	chr2:78264616-78264617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551815381	chr2:78264652-78264653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2177981	chr2:78264684-78264685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs550010429	chr2:78264721-78264722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570117991	chr2:78264752-78264753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190651705	chr2:78265027-78265028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183351331	chr2:78265168-78265169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534736237	chr2:78265174-78265175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555911492	chr2:78270846-78270847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567517058	chr2:78270851-78270852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536737051	chr2:78270865-78270866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550810452	chr2:78270875-78270876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550333935	chr2:78270906-78270907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570044092	chr2:78270915-78270916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377139202	chr2:78270938-78270939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182373054	chr2:78270941-78270942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569100251	chr2:78270986-78270987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs34798582	chr2:78271061-78271062	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs35605697	chr2:78271083-78271084	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs185422937	chr2:78271092-78271093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188222023	chr2:78271100-78271101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1527188	chr2:78271153-78271154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58240200	chr2:78271185-78271186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs386390542	chr2:78271186-78271187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs386390543	chr2:78271187-78271188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs397976388	chr2:78271188-78271189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78263800-78264000	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr2:78263800-78264800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:78265000-78265200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr2:78270800-78271000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr2:78271000-78272200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:78272800-78274200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:78282400-78284000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:78286000-78289600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr2:78288200-78288600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:78288200-78288800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr2:78288200-78288800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr2:78288200-78289000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr2:78288200-78289400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:78288400-78289200	Enhancers	Fetal Muscle Leg	muscle
15	chr2:78288400-78289600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:78288600-78289600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:78288800-78289200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr2:78289600-78293200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:78293200-78293400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:78295800-78296200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr2:78296200-78305400	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr2:78298000-78298800	Enhancers	Fetal Lung	lung
23	chr2:78301200-78306400	Weak transcription	HepG2	liver
24	chr2:78303600-78305600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr2:78304600-78305600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:78305000-78305200	Enhancers	Brain Substantia Nigra	brain
27	chr2:78305000-78305400	Enhancers	H1 Cell Line	embryonic stem cell
28	chr2:78305000-78305400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr2:78305000-78306800	Enhancers	Brain Cingulate Gyrus	brain
30	chr2:78305200-78306000	Weak transcription	Brain Substantia Nigra	brain
31	chr2:78305400-78306200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr2:78305400-78306600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr2:78305800-78306800	Enhancers	Brain Hippocampus Middle	brain
34	chr2:78306000-78306400	Enhancers	Brain Substantia Nigra	brain
35	chr2:78306800-78307000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr2:78309800-78311200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:78322800-78324000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr2:78324000-78324200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
39	chr2:78326200-78326800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:78330200-78332400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr2:78330600-78331600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:78331000-78331600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:78331600-78332800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:78332800-78333600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr2:78335000-78337600	Enhancers	Liver	Liver
46	chr2:78336000-78336600	Active TSS	Fetal Heart	heart
47	chr2:78336200-78337200	Enhancers	HepG2	liver
48	chr2:78337200-78339000	Weak transcription	HepG2	liver
49	chr2:78339000-78339400	Strong transcription	HepG2	liver
50	chr2:78339400-78341200	Weak transcription	HepG2	liver

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