Variant report

Variant	nsv834481
Chromosome Location	chr2:183189758-183339577
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	BCL3	chr2:183216612-183216884	GM12878	blood:	n/a	n/a
2	BCL3	chr2:183216207-183216552	GM12878	blood:	n/a	n/a
3	BCL3	chr2:183231250-183231948	A549	lung:	n/a	n/a
4	BRCA1	chr2:183231396-183231828	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr2:183249509-183249933	HCT-116	colon:	n/a	n/a
6	CBX3	chr2:183237279-183237999	HCT-116	colon:	n/a	n/a
7	CBX3	chr2:183237165-183238178	HCT-116	colon:	n/a	n/a
8	CEBPB	chr2:183306725-183306989	HepG2	liver:	n/a	chr2:183306851-183306862
9	CEBPB	chr2:183312572-183312926	IMR90	lung:	n/a	n/a
10	CEBPB	chr2:183231373-183231769	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:183242166-183242424	A549	lung:	n/a	chr2:183242227-183242238
12	CEBPB	chr2:183223154-183223442	A549	lung:	n/a	chr2:183223293-183223304
13	CEBPB	chr2:183309586-183309939	Hela-S3	cervix:	n/a	chr2:183309774-183309786
14	CEBPB	chr2:183192199-183192482	HepG2	liver:	n/a	chr2:183192322-183192333
15	CEBPB	chr2:183312590-183312919	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:183290871-183291204	Hela-S3	cervix:	n/a	chr2:183291025-183291038 chr2:183291025-183291038 chr2:183291025-183291036
17	CEBPB	chr2:183231290-183231799	A549	lung:	n/a	n/a
18	CEBPB	chr2:183306717-183307024	IMR90	lung:	n/a	chr2:183306851-183306862
19	CEBPB	chr2:183300983-183301478	A549	lung:	n/a	chr2:183301184-183301195
20	CEBPB	chr2:183301075-183301350	Hela-S3	cervix:	n/a	chr2:183301184-183301195
21	CEBPB	chr2:183230740-183231893	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:183233137-183233597	Hela-S3	cervix:	n/a	chr2:183233373-183233386
23	CEBPB	chr2:183306786-183306959	H1-hESC	embryonic stem cell:	n/a	chr2:183306851-183306862
24	CEBPB	chr2:183231573-183231680	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:183258279-183258325	A549	lung:	n/a	n/a
26	CEBPB	chr2:183276309-183276515	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:183261729-183261849	HepG2	liver:	n/a	chr2:183261752-183261763
28	CEBPB	chr2:183220588-183220918	A549	lung:	n/a	chr2:183220847-183220858 chr2:183220736-183220747 chr2:183220734-183220747 chr2:183220736-183220745 chr2:183220734-183220745 chr2:183220847-183220860
29	CEBPB	chr2:183220617-183220859	K562	blood:	n/a	chr2:183220847-183220858 chr2:183220736-183220747 chr2:183220734-183220747 chr2:183220736-183220745 chr2:183220734-183220745
30	CEBPB	chr2:183237375-183237812	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:183233122-183233566	A549	lung:	n/a	chr2:183233373-183233386
32	CEBPB	chr2:183242114-183242413	HepG2	liver:	n/a	chr2:183242227-183242238
33	CEBPB	chr2:183301036-183301362	IMR90	lung:	n/a	chr2:183301184-183301195
34	CEBPB	chr2:183310193-183310620	Hela-S3	cervix:	n/a	chr2:183310406-183310418
35	CEBPB	chr2:183220608-183220890	H1-hESC	embryonic stem cell:	n/a	chr2:183220847-183220858 chr2:183220736-183220747 chr2:183220734-183220747 chr2:183220736-183220745 chr2:183220734-183220745 chr2:183220847-183220860
36	CEBPB	chr2:183233194-183233525	A549	lung:	n/a	chr2:183233373-183233386
37	CEBPB	chr2:183242136-183242437	IMR90	lung:	n/a	chr2:183242227-183242238
38	CEBPB	chr2:183220591-183220912	Hela-S3	cervix:	n/a	chr2:183220847-183220858 chr2:183220736-183220747 chr2:183220734-183220747 chr2:183220736-183220745 chr2:183220734-183220745 chr2:183220847-183220860
39	CEBPB	chr2:183189446-183189798	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr2:183189356-183189886	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:183290856-183291196	HepG2	liver:	n/a	chr2:183291025-183291038 chr2:183291025-183291038 chr2:183291025-183291036
42	CEBPB	chr2:183258155-183258426	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:183231308-183231851	A549	lung:	n/a	n/a
44	CEBPB	chr2:183220570-183220911	HepG2	liver:	n/a	chr2:183220847-183220858 chr2:183220736-183220747 chr2:183220734-183220747 chr2:183220736-183220745 chr2:183220734-183220745 chr2:183220847-183220860
45	CEBPB	chr2:183306794-183306917	A549	lung:	n/a	chr2:183306851-183306862
46	CEBPB	chr2:183214050-183214561	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr2:183281110-183281236	A549	lung:	n/a	n/a
48	CEBPB	chr2:183290839-183291219	IMR90	lung:	n/a	chr2:183291025-183291038 chr2:183291025-183291038 chr2:183291025-183291036
49	CEBPB	chr2:183301066-183301332	A549	lung:	n/a	chr2:183301184-183301195
50	CEBPB	chr2:183301109-183301257	H1-hESC	embryonic stem cell:	n/a	chr2:183301184-183301195

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183244218-183244268	NB4	blood:	n/a
2	chr2:183312755-183312805	PFSK-1	brain:	n/a
3	chr2:183224447-183224497	AG10803	skin:	n/a
4	chr2:183321813-183321863	HCF	heart:	n/a
5	chr2:183321813-183321863	HRCEpiC	kidney:	n/a
6	chr2:183277810-183277860	NB4	blood:	n/a
7	chr2:183244218-183244268	HEEpiC	esophagus:	n/a
8	chr2:183291758-183291808	HEEpiC	esophagus:	n/a
9	chr2:183292922-183292972	Jurkat	blood:	n/a
10	chr2:183224447-183224497	NT2-D1	testis:	n/a
11	chr2:183312755-183312805	ovcar-3	ovarian:	n/a
12	chr2:183224447-183224497	PANC-1	pancreas:	n/a
13	chr2:183291758-183291808	HRE	kidney:	n/a
14	chr2:183224447-183224497	HRPEpiC	eye:	n/a
15	chr2:183292922-183292972	HMEC	breast:	n/a
16	chr2:183321813-183321863	IMR90	lung:	fetal
17	chr2:183292092-183292142	SAEC	small airway:	n/a
18	chr2:183277810-183277860	HPAEpiC	pulmonary alveolar:	n/a
19	chr2:183291758-183291808	SK-N-MC	brain:	n/a
20	chr2:183291758-183291808	GM12892	blood:	n/a
21	chr2:183312755-183312805	HL-60	blood:	n/a
22	chr2:183321813-183321863	HAEpiC	amniotic membrane:	n/a
23	chr2:183291758-183291808	AG10803	skin:	n/a
24	chr2:183244218-183244268	HL-60	blood:	n/a
25	chr2:183292922-183292972	H1-hESC	embryonic stem cell:	embryo
26	chr2:183292092-183292142	HL-60	blood:	n/a
27	chr2:183291758-183291808	U87	brain:	n/a
28	chr2:183291758-183291808	CMK	blood:	n/a
29	chr2:183321813-183321863	NHDF-neo	bronchial:	n/a
30	chr2:183312755-183312805	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:183321813-183321863	RPTEC	kidney:	n/a
32	chr2:183292092-183292142	BE2_C	brain:	n/a
33	chr2:183291758-183291808	Caco-2	colon:	n/a
34	chr2:183224447-183224497	NHDF-neo	bronchial:	n/a
35	chr2:183244218-183244268	AG04449	skin:	fetal
36	chr2:183292092-183292142	GM12891	blood:	n/a
37	chr2:183277810-183277860	AG04449	skin:	fetal
38	chr2:183292092-183292142	GM06990	blood:	n/a
39	chr2:183277810-183277860	MCF-7	breast:	n/a
40	chr2:183277810-183277860	HCPEpiC	choroid plexus:	n/a
41	chr2:183277810-183277860	BJ	skin:	n/a
42	chr2:183312755-183312805	HCF	heart:	n/a
43	chr2:183277810-183277860	H1-hESC	embryonic stem cell:	embryo
44	chr2:183277810-183277860	PANC-1	pancreas:	n/a
45	chr2:183312755-183312805	HAEpiC	amniotic membrane:	n/a
46	chr2:183277810-183277860	SKMC	muscle:	n/a
47	chr2:183277810-183277860	PrEC	prostate:	n/a
48	chr2:183292922-183292972	HCPEpiC	choroid plexus:	n/a
49	chr2:183277810-183277860	SK-N-SH	brain:	n/a
50	chr2:183277810-183277860	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:183223904..183227236-chr2:183228797..183232195,3	K562	blood:
2	chr2:183296401..183298106-chr2:183311342..183313093,2	K562	blood:
3	chr2:183296401..183298106-chr2:183311342..183313093,2	K562	blood:
4	chr2:183279805..183282576-chr2:183283431..183285947,2	MCF-7	breast:
5	chr2:183279201..183281730-chr2:183282038..183284679,2	MCF-7	breast:
6	chr2:183220786..183225092-chr2:183225248..183228403,3	MCF-7	breast:
7	chr2:183261575..183263356-chr2:183271922..183273654,2	K562	blood:
8	chr2:183220786..183225092-chr2:183225248..183228403,3	MCF-7	breast:
9	chr2:183297531..183299912-chr2:183299956..183302678,2	K562	blood:
10	chr2:183335532..183337618-chr2:183340373..183342974,2	K562	blood:
11	chr2:183279805..183282576-chr2:183283431..183285947,2	MCF-7	breast:
12	chr2:183285134..183287339-chr2:183293289..183296061,2	K562	blood:
13	chr12:82936658..82939200-chr2:183214684..183217154,2	MCF-7	breast:
14	chr2:183285134..183287339-chr2:183293289..183296061,2	K562	blood:
15	chr2:183325057..183326924-chr2:183328449..183330084,2	K562	blood:
16	chr2:183261575..183263356-chr2:183271922..183273654,2	K562	blood:
17	chr2:183279201..183281730-chr2:183282038..183284679,2	MCF-7	breast:
18	chr2:183223904..183227236-chr2:183228797..183232195,3	K562	blood:
19	chr2:183290653..183293627-chr2:183296463..183299216,2	K562	blood:
20	chr2:183291063..183292586-chr2:183298159..183300836,2	MCF-7	breast:
21	chr2:183325057..183326924-chr2:183328449..183330084,2	K562	blood:
22	chr2:183297531..183299912-chr2:183299956..183302678,2	K562	blood:

Variant related genes	Relation type
PDE1A	TF binding region
PDE1A	CpG island
ENSG00000115252	chromatin interactions

Extended variants
information (count: 5676 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:5676 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557023849	chr2:183189809-183189810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144922924	chr2:183189810-183189811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563566298	chr2:183189834-183189835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185645500	chr2:183189867-183189868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541396572	chr2:183189917-183189918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559456143	chr2:183189968-183189969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573493344	chr2:183190033-183190034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545670766	chr2:183190064-183190065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150344329	chr2:183190081-183190082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575634080	chr2:183190082-183190083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35485908	chr2:183190087-183190088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568889642	chr2:183190118-183190119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531119099	chr2:183190148-183190149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550731567	chr2:183190156-183190157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116343975	chr2:183190161-183190162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190751476	chr2:183190190-183190191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs833176	chr2:183190294-183190295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs113129300	chr2:183190334-183190335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192255879	chr2:183190335-183190336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184655873	chr2:183190370-183190371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201855415	chr2:183190371-183190372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568749792	chr2:183190382-183190383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537629720	chr2:183190409-183190410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112675720	chr2:183190444-183190445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574097315	chr2:183190467-183190468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553676127	chr2:183190471-183190472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115598100	chr2:183190509-183190510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11690853	chr2:183190554-183190555	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573271516	chr2:183190574-183190575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140297066	chr2:183190588-183190589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565564388	chr2:183190608-183190609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575936734	chr2:183190643-183190644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544840402	chr2:183190665-183190666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561290014	chr2:183190712-183190713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529804975	chr2:183190719-183190720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150338618	chr2:183190723-183190724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560138135	chr2:183190730-183190731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138012186	chr2:183190781-183190782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531004442	chr2:183190787-183190788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35372886	chr2:183190848-183190849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572831664	chr2:183190849-183190850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs397791417	chr2:183190854-183190855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188543498	chr2:183190863-183190864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531469032	chr2:183190892-183190893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531091638	chr2:183190914-183190915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548375358	chr2:183190927-183190928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181220501	chr2:183190953-183190954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185714676	chr2:183190990-183190991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188992511	chr2:183191004-183191005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566908123	chr2:183191015-183191016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183188200-183190200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:183188400-183190200	Enhancers	Hela-S3	cervix
3	chr2:183188600-183195400	Weak transcription	Aorta	Aorta
4	chr2:183188800-183197400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:183189200-183189800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:183189200-183189800	Enhancers	Fetal Kidney	kidney
7	chr2:183189200-183190000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:183189200-183190200	Enhancers	Muscle Satellite Cultured Cells	--
9	chr2:183189400-183189800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:183189400-183195400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr2:183189600-183191800	Weak transcription	Osteobl	bone
12	chr2:183189800-183195200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:183190000-183195200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:183190200-183191200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:183190200-183191200	Weak transcription	Hela-S3	cervix
16	chr2:183190200-183195400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr2:183191200-183191400	Enhancers	Hela-S3	cervix
18	chr2:183191200-183192000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:183191600-183192000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr2:183192000-183194600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr2:183192600-183192800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
22	chr2:183193000-183195200	Weak transcription	Osteobl	bone
23	chr2:183194600-183196400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:183195200-183195400	Enhancers	Osteobl	bone
25	chr2:183195200-183195800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:183195200-183195800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:183195200-183195800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr2:183195400-183195600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:183195400-183195800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr2:183195400-183195800	Enhancers	Right Atrium	heart
31	chr2:183195400-183195800	Enhancers	NHDF-Ad	bronchial
32	chr2:183195400-183195800	Flanking Active TSS	Osteobl	bone
33	chr2:183195400-183196000	Enhancers	Aorta	Aorta
34	chr2:183195600-183195800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:183195800-183196000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:183195800-183196200	Enhancers	Osteobl	bone
37	chr2:183196000-183199000	Weak transcription	Aorta	Aorta
38	chr2:183197400-183197600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr2:183197600-183203000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:183199800-183216800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:183202200-183202400	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr2:183202400-183204400	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr2:183203200-183203400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:183203200-183203600	Enhancers	Esophagus	oesophagus
45	chr2:183203800-183204200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr2:183203800-183204400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:183204400-183204600	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr2:183204400-183205400	Enhancers	Colon Smooth Muscle	Colon
49	chr2:183207800-183208000	Enhancers	Fetal Kidney	kidney
50	chr2:183210000-183210400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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