Variant report

Variant	nsv459956
Chromosome Location	chr2:183170516-183204369
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	CEBPB	chr2:183189399-183189755	IMR90	lung:	n/a	n/a
2	CEBPB	chr2:183189356-183189886	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr2:183189358-183189746	ECC-1	luminal epithelium:	n/a	n/a
4	CEBPB	chr2:183183695-183183994	A549	lung:	n/a	chr2:183183846-183183857 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183858 chr2:183183847-183183856 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183856 chr2:183183845-183183856 chr2:183183847-183183856
5	CEBPB	chr2:183189378-183189696	A549	lung:	n/a	n/a
6	CEBPB	chr2:183192199-183192482	HepG2	liver:	n/a	chr2:183192322-183192333
7	CEBPB	chr2:183189446-183189798	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr2:183183528-183184081	Hela-S3	cervix:	n/a	chr2:183183846-183183857 chr2:183184039-183184052 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183858 chr2:183183847-183183856 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183856 chr2:183183845-183183856 chr2:183183847-183183856
9	CEBPB	chr2:183183578-183184085	IMR90	lung:	n/a	chr2:183183846-183183857 chr2:183184039-183184052 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183858 chr2:183183847-183183856 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183856 chr2:183183845-183183856 chr2:183183847-183183856
10	CEBPB	chr2:183183671-183184069	HepG2	liver:	n/a	chr2:183183846-183183857 chr2:183184039-183184052 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183858 chr2:183183847-183183856 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183856 chr2:183183845-183183856 chr2:183183847-183183856
11	CEBPB	chr2:183183738-183183975	K562	blood:	n/a	chr2:183183846-183183857 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183858 chr2:183183847-183183856 chr2:183183847-183183856 chr2:183183845-183183858 chr2:183183845-183183856 chr2:183183845-183183856 chr2:183183847-183183856
12	CEBPZ	chr2:183189147-183189164	HepG2	liver:	n/a	n/a
13	CHD2	chr2:183189408-183189764	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr2:183172052-183172055	GM10248	blood:	n/a	n/a
15	CTCF	chr2:183171981-183172047	GM10248	blood:	n/a	n/a
16	CTCF	chr2:183179080-183179230	HBMEC	blood vessel:	n/a	n/a
17	EP300	chr2:183184415-183184615	Hela-S3	cervix:	n/a	chr2:183184512-183184522
18	EP300	chr2:183183540-183184056	Hela-S3	cervix:	n/a	chr2:183184037-183184051 chr2:183183843-183183857
19	EP300	chr2:183189323-183189881	Hela-S3	cervix:	n/a	n/a
20	ESR1	chr2:183189406-183189869	ECC-1	luminal epithelium:	n/a	n/a
21	ESR1	chr2:183189396-183189945	ECC-1	luminal epithelium:	n/a	n/a
22	ESR1	chr2:183189377-183189940	ECC-1	luminal epithelium:	n/a	n/a
23	FAM48A	chr2:183192299-183192414	GM12878	blood:	n/a	n/a
24	FOS	chr2:183183450-183183878	HUVEC	blood vessel:	n/a	chr2:183183640-183183651 chr2:183183661-183183671 chr2:183183661-183183671 chr2:183183660-183183671
25	FOS	chr2:183189413-183189784	MCF10A-Er-Src	breast:	n/a	chr2:183189546-183189556
26	FOS	chr2:183183477-183183883	MCF10A-Er-Src	breast:	n/a	chr2:183183640-183183651 chr2:183183661-183183671 chr2:183183661-183183671 chr2:183183660-183183671
27	FOS	chr2:183189407-183189730	MCF10A-Er-Src	breast:	n/a	chr2:183189546-183189556
28	FOS	chr2:183184458-183184584	MCF10A-Er-Src	breast:	n/a	chr2:183184482-183184494
29	FOS	chr2:183183526-183183816	MCF10A-Er-Src	breast:	n/a	chr2:183183640-183183651 chr2:183183661-183183671 chr2:183183661-183183671 chr2:183183660-183183671
30	FOS	chr2:183189403-183189816	MCF10A-Er-Src	breast:	n/a	chr2:183189546-183189556
31	FOS	chr2:183189459-183189779	MCF10A-Er-Src	breast:	n/a	chr2:183189546-183189556
32	FOS	chr2:183183481-183184009	MCF10A-Er-Src	breast:	n/a	chr2:183183640-183183651 chr2:183183661-183183671 chr2:183183661-183183671 chr2:183183660-183183671
33	FOS	chr2:183183456-183184094	MCF10A-Er-Src	breast:	n/a	chr2:183183640-183183651 chr2:183183661-183183671 chr2:183183661-183183671 chr2:183183660-183183671
34	GATA2	chr2:183179100-183179511	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr2:183185138-183185186	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr2:183189461-183189765	A549	lung:	n/a	chr2:183189536-183189543
37	GATA3	chr2:183176508-183176636	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr2:183191583-183191720	MCF-7	breast:	n/a	n/a
39	JUN	chr2:183195385-183195525	HepG2	liver:	n/a	chr2:183195432-183195445
40	JUN	chr2:183182145-183182345	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chr2:183195303-183195614	HepG2	liver:	n/a	n/a
42	KAP1	chr2:183203516-183203995	HEK293	kidney:	n/a	n/a
43	KAP1	chr2:183184401-183184694	U2OS	brain:	n/a	n/a
44	MAFK	chr2:183176308-183176508	IMR90	lung:	n/a	n/a
45	MAFK	chr2:183176276-183176518	HepG2	liver:	n/a	n/a
46	MXI1	chr2:183185440-183185445	K562	blood:	n/a	n/a
47	MXI1	chr2:183183536-183184034	Hela-S3	cervix:	n/a	n/a
48	MYC	chr2:183189504-183189663	MCF10A-Er-Src	breast:	n/a	n/a
49	MYC	chr2:183189452-183189715	MCF10A-Er-Src	breast:	n/a	n/a
50	NFIC	chr2:183189496-183189978	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183183274-183183324	HRCEpiC	kidney:	n/a
2	chr2:183183274-183183324	MCF-7	breast:	n/a
3	chr2:183183274-183183324	NHBE	bronchial:	n/a
4	chr2:183183274-183183324	HCPEpiC	choroid plexus:	n/a
5	chr2:183183274-183183324	HCF	heart:	n/a
6	chr2:183183274-183183324	HCM	heart:	n/a
7	chr2:183183274-183183324	HUVEC	blood vessel:	n/a
8	chr2:183183274-183183324	RPTEC	kidney:	n/a
9	chr2:183183274-183183324	Caco-2	colon:	n/a
10	chr2:183183274-183183324	SK-N-SH	brain:	n/a
11	chr2:183183274-183183324	NHDF-neo	bronchial:	n/a
12	chr2:183183274-183183324	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:183183274-183183324	NB4	blood:	n/a
14	chr2:183183274-183183324	HCT-116	colon:	n/a
15	chr2:183183274-183183324	K562	blood:	n/a
16	chr2:183183274-183183324	GM12878	blood:	n/a
17	chr2:183183274-183183324	PANC-1	pancreas:	n/a
18	chr2:183183274-183183324	T-47D	breast:	n/a
19	chr2:183183274-183183324	GM06990	blood:	n/a
20	chr2:183183274-183183324	BJ	skin:	n/a
21	chr2:183183274-183183324	IMR90	lung:	fetal
22	chr2:183183274-183183324	AG04450	lung:	fetal
23	chr2:183183274-183183324	ovcar-3	ovarian:	n/a
24	chr2:183183274-183183324	SKMC	muscle:	n/a
25	chr2:183183274-183183324	AG10803	skin:	n/a
26	chr2:183183274-183183324	GM12892	blood:	n/a
27	chr2:183183274-183183324	BE2_C	brain:	n/a
28	chr2:183183274-183183324	Hepatocyte	liver:	n/a
29	chr2:183183274-183183324	NH-A	brain:	n/a
30	chr2:183183274-183183324	HEEpiC	esophagus:	n/a
31	chr2:183183274-183183324	HEK293	kidney:	embryo
32	chr2:183183274-183183324	HL-60	blood:	n/a
33	chr2:183183274-183183324	U87	brain:	n/a
34	chr2:183183274-183183324	AG09319	gingival:	n/a
35	chr2:183183274-183183324	A549	lung:	n/a
36	chr2:183183274-183183324	LNCaP	prostate:	n/a
37	chr2:183183274-183183324	GM19239	blood:	n/a
38	chr2:183183274-183183324	PrEC	prostate:	n/a
39	chr2:183183274-183183324	PFSK-1	brain:	n/a
40	chr2:183183274-183183324	AoSMC	blood vessel:	n/a
41	chr2:183183274-183183324	ProgFib	skin:	n/a
42	chr2:183183274-183183324	SK-N-SH_RA	brain:	n/a
43	chr2:183183274-183183324	MCF10A-Er-Src	breast:	n/a
44	chr2:183183274-183183324	HNPCEpiC	eye:	n/a
45	chr2:183183274-183183324	HRPEpiC	eye:	n/a
46	chr2:183183274-183183324	CMK	blood:	n/a
47	chr2:183183274-183183324	HIPEpiC	eye:	n/a
48	chr2:183183274-183183324	HRE	kidney:	n/a
49	chr2:183183274-183183324	Hela-S3	cervix:	n/a
50	chr2:183183274-183183324	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:183179551..183180178-chr3:111918314..111918885,2	MCF-7	breast:
2	chr2:183172864..183175852-chr2:183181543..183183109,2	K562	blood:
3	chr2:183182727..183184381-chr2:183186031..183187729,2	K562	blood:
4	chr2:183182727..183184381-chr2:183186031..183187729,2	K562	blood:
5	chr2:183172864..183175852-chr2:183181543..183183109,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R1C-3	chr2:183179011-183179269	NONHSAT075907

Variant related genes	Relation type
RN7SL267P	TF binding region
RN7SL267P	CpG island

Extended variants
information (count: 1168 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:1168 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs833128	chr2:183170516-183170517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372692846	chr2:183170521-183170522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546501396	chr2:183170540-183170541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140520865	chr2:183170554-183170555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77157065	chr2:183170632-183170633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544748535	chr2:183170636-183170637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78129183	chr2:183170662-183170663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370642453	chr2:183170674-183170675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144288592	chr2:183170700-183170701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376175538	chr2:183170817-183170818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527306452	chr2:183170893-183170894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546961879	chr2:183170897-183170898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140308476	chr2:183170955-183170956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570093514	chr2:183170979-183170980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192633908	chr2:183171048-183171049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556415329	chr2:183171076-183171077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62190530	chr2:183171100-183171101	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs535593030	chr2:183171130-183171131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376128800	chr2:183171139-183171140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368777376	chr2:183171183-183171184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578122902	chr2:183171186-183171187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148572435	chr2:183171204-183171205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199881150	chr2:183171206-183171207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62190531	chr2:183171208-183171209	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs201039371	chr2:183171227-183171228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74344768	chr2:183171228-183171229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2577654	chr2:183171231-183171232	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs554240319	chr2:183171247-183171248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577298269	chr2:183171261-183171262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373857033	chr2:183171280-183171281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2623412	chr2:183171297-183171298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs563149065	chr2:183171319-183171320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188502490	chr2:183171356-183171357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542373981	chr2:183171382-183171383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561468103	chr2:183171385-183171386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527413663	chr2:183171417-183171418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547075667	chr2:183171467-183171468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181218395	chr2:183171496-183171497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532764092	chr2:183171556-183171557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116630197	chr2:183171559-183171560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528459918	chr2:183171560-183171561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549006726	chr2:183171615-183171616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113048982	chr2:183171637-183171638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200928739	chr2:183171652-183171653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72897100	chr2:183171677-183171678	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs2577655	chr2:183171706-183171707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs571132729	chr2:183171763-183171764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554303639	chr2:183171778-183171779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577312336	chr2:183171788-183171789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185714805	chr2:183171793-183171794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Pancreatic cancer	17952125	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183158800-183183200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:183168400-183174400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:183174600-183174800	Enhancers	Colon Smooth Muscle	Colon
4	chr2:183175000-183175600	Weak transcription	Colon Smooth Muscle	Colon
5	chr2:183175400-183175600	Weak transcription	Aorta	Aorta
6	chr2:183175600-183175800	Enhancers	Aorta	Aorta
7	chr2:183175600-183175800	Enhancers	Colon Smooth Muscle	Colon
8	chr2:183175600-183175800	Enhancers	Right Atrium	heart
9	chr2:183175800-183184600	Weak transcription	Right Atrium	heart
10	chr2:183175800-183188400	Weak transcription	Aorta	Aorta
11	chr2:183179800-183183400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:183181600-183186200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr2:183181800-183182600	Enhancers	Colon Smooth Muscle	Colon
14	chr2:183182000-183182200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr2:183182000-183182400	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr2:183182200-183182400	Enhancers	Brain Angular Gyrus	brain
17	chr2:183182200-183182400	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr2:183182200-183183200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr2:183182200-183185000	Enhancers	NHDF-Ad	bronchial
20	chr2:183182600-183183000	Weak transcription	Colon Smooth Muscle	Colon
21	chr2:183182600-183183800	Weak transcription	Brain Angular Gyrus	brain
22	chr2:183182800-183186000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr2:183183000-183183200	Enhancers	Colon Smooth Muscle	Colon
24	chr2:183183000-183183400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr2:183183000-183183400	Enhancers	NHLF	lung
26	chr2:183183000-183183600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:183183000-183183600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr2:183183000-183184800	Enhancers	Osteobl	bone
29	chr2:183183000-183185400	Enhancers	Hela-S3	cervix
30	chr2:183183200-183183400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr2:183183200-183183400	Enhancers	Fetal Stomach	stomach
32	chr2:183183200-183183800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:183183200-183183800	Enhancers	Brain Substantia Nigra	brain
34	chr2:183183200-183184000	Enhancers	HUVEC	blood vessel
35	chr2:183183200-183184400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr2:183183200-183184600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr2:183183200-183184600	Weak transcription	Colon Smooth Muscle	Colon
38	chr2:183183200-183184600	Enhancers	NH-A	brain
39	chr2:183183200-183184800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:183183200-183185200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr2:183183400-183183600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:183183400-183183600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:183183400-183184600	Weak transcription	Fetal Stomach	stomach
44	chr2:183183600-183184000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:183183600-183184600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr2:183183800-183184200	Weak transcription	Brain Substantia Nigra	brain
47	chr2:183183800-183184400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr2:183183800-183184600	Enhancers	Brain Angular Gyrus	brain
49	chr2:183184000-183186400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:183184200-183184600	Enhancers	Brain Substantia Nigra	brain

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