Variant report

Variant	nsv1008825
Chromosome Location	chr2:183067339-183228668
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	ARID3A	chr2:183105472-183105968	HepG2	liver:	n/a	n/a
2	ATF2	chr2:183110648-183110961	GM12878	blood:	n/a	n/a
3	BACH1	chr2:183128564-183128593	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:183107362-183107550	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:183110630-183111009	GM12878	blood:	n/a	n/a
6	BATF	chr2:183105570-183105896	GM12878	blood:	n/a	n/a
7	BATF	chr2:183105612-183105996	GM12878	blood:	n/a	n/a
8	BATF	chr2:183110684-183111025	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:183105580-183105957	GM12878	blood:	n/a	chr2:183105754-183105763
10	BCL11A	chr2:183105671-183105923	GM12878	blood:	n/a	chr2:183105754-183105763
11	BCL11A	chr2:183110662-183110954	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:183110738-183110944	GM12878	blood:	n/a	n/a
13	BCL3	chr2:183216612-183216884	GM12878	blood:	n/a	n/a
14	BCL3	chr2:183216207-183216552	GM12878	blood:	n/a	n/a
15	BCLAF1	chr2:183105461-183106039	GM12878	blood:	n/a	chr2:183105754-183105763
16	BHLHE40	chr2:183090280-183090425	GM12878	blood:	n/a	n/a
17	BRCA1	chr2:183165364-183166161	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:183227778-183227849	A549	lung:	n/a	n/a
19	CEBPB	chr2:183164402-183164698	IMR90	lung:	n/a	chr2:183164499-183164510
20	CEBPB	chr2:183220617-183220859	K562	blood:	n/a	chr2:183220847-183220858 chr2:183220736-183220747 chr2:183220734-183220747 chr2:183220736-183220745 chr2:183220734-183220745
21	CEBPB	chr2:183214050-183214561	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:183224444-183225373	A549	lung:	n/a	chr2:183225074-183225085
23	CEBPB	chr2:183192199-183192482	HepG2	liver:	n/a	chr2:183192322-183192333
24	CEBPB	chr2:183164351-183164700	HepG2	liver:	n/a	chr2:183164499-183164510
25	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
26	CEBPB	chr2:183151192-183151252	HepG2	liver:	n/a	n/a
27	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
28	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
29	CEBPB	chr2:183107052-183107283	A549	lung:	n/a	n/a
30	CEBPB	chr2:183224893-183225363	A549	lung:	n/a	chr2:183225074-183225085
31	CEBPB	chr2:183189356-183189886	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:183105637-183106115	HepG2	liver:	n/a	n/a
33	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
34	CEBPB	chr2:183166893-183167420	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:183224464-183225244	IMR90	lung:	n/a	chr2:183225074-183225085
36	CEBPB	chr2:183137459-183137531	HepG2	liver:	n/a	chr2:183137511-183137522
37	CEBPB	chr2:183224771-183225487	A549	lung:	n/a	chr2:183225074-183225085
38	CEBPB	chr2:183189399-183189755	IMR90	lung:	n/a	n/a
39	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
40	CEBPB	chr2:183098027-183098213	HepG2	liver:	n/a	chr2:183098089-183098100
41	CEBPB	chr2:183164424-183164659	A549	lung:	n/a	chr2:183164499-183164510
42	CEBPB	chr2:183107018-183107332	HepG2	liver:	n/a	n/a
43	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
44	CEBPB	chr2:183094006-183094366	IMR90	lung:	n/a	chr2:183094264-183094275 chr2:183094268-183094279 chr2:183094025-183094038 chr2:183094264-183094275
45	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
46	CEBPB	chr2:183164331-183164782	Hela-S3	cervix:	n/a	chr2:183164499-183164510
47	CEBPB	chr2:183166916-183167207	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:183223139-183223414	HepG2	liver:	n/a	chr2:183223293-183223304
49	CEBPB	chr2:183189378-183189696	A549	lung:	n/a	n/a
50	CEBPB	chr2:183189446-183189798	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183107046-183107096	IMR90	lung:	fetal
2	chr2:183107046-183107096	HRPEpiC	eye:	n/a
3	chr2:183107220-183107270	HCF	heart:	n/a
4	chr2:183106125-183106175	NH-A	brain:	n/a
5	chr2:183123847-183123897	HCT-116	colon:	n/a
6	chr2:183086277-183086327	SK-N-MC	brain:	n/a
7	chr2:183123847-183123897	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:183106125-183106175	GM06990	blood:	n/a
9	chr2:183183274-183183324	NB4	blood:	n/a
10	chr2:183107046-183107096	SKMC	muscle:	n/a
11	chr2:183106125-183106175	K562	blood:	n/a
12	chr2:183123847-183123897	NB4	blood:	n/a
13	chr2:183183274-183183324	MCF10A-Er-Src	breast:	n/a
14	chr2:183106125-183106175	SAEC	small airway:	n/a
15	chr2:183224447-183224497	ProgFib	skin:	n/a
16	chr2:183224447-183224497	HCPEpiC	choroid plexus:	n/a
17	chr2:183107220-183107270	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:183086277-183086327	AG09319	gingival:	n/a
19	chr2:183224447-183224497	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:183183274-183183324	K562	blood:	n/a
21	chr2:183183274-183183324	HIPEpiC	eye:	n/a
22	chr2:183183274-183183324	ECC-1	luminal epithelium:	n/a
23	chr2:183224447-183224497	HCT-116	colon:	n/a
24	chr2:183107220-183107270	SK-N-SH_RA	brain:	n/a
25	chr2:183086277-183086327	PANC-1	pancreas:	n/a
26	chr2:183123847-183123897	CMK	blood:	n/a
27	chr2:183123847-183123897	ProgFib	skin:	n/a
28	chr2:183106125-183106175	Caco-2	colon:	n/a
29	chr2:183224447-183224497	PrEC	prostate:	n/a
30	chr2:183224447-183224497	SK-N-SH_RA	brain:	n/a
31	chr2:183107046-183107096	SK-N-MC	brain:	n/a
32	chr2:183183274-183183324	GM19239	blood:	n/a
33	chr2:183107046-183107096	SAEC	small airway:	n/a
34	chr2:183107046-183107096	GM06990	blood:	n/a
35	chr2:183123847-183123897	ovcar-3	ovarian:	n/a
36	chr2:183107220-183107270	H1-hESC	embryonic stem cell:	embryo
37	chr2:183107046-183107096	NH-A	brain:	n/a
38	chr2:183224447-183224497	NB4	blood:	n/a
39	chr2:183107046-183107096	HEEpiC	esophagus:	n/a
40	chr2:183086277-183086327	HCT-116	colon:	n/a
41	chr2:183107046-183107096	CMK	blood:	n/a
42	chr2:183107046-183107096	GM12892	blood:	n/a
43	chr2:183183274-183183324	ovcar-3	ovarian:	n/a
44	chr2:183123847-183123897	HEK293	kidney:	embryo
45	chr2:183086277-183086327	HRE	kidney:	n/a
46	chr2:183086277-183086327	BE2_C	brain:	n/a
47	chr2:183107220-183107270	ECC-1	luminal epithelium:	n/a
48	chr2:183106125-183106175	ECC-1	luminal epithelium:	n/a
49	chr2:183106125-183106175	GM12891	blood:	n/a
50	chr2:183183274-183183324	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:183223904..183227236-chr2:183228797..183232195,3	K562	blood:
2	chr2:183103040..183104711-chr2:183106820..183108898,2	K562	blood:
3	chr2:183182727..183184381-chr2:183186031..183187729,2	K562	blood:
4	chr2:183172864..183175852-chr2:183181543..183183109,2	K562	blood:
5	chr2:183139290..183141946-chr2:183155474..183158091,2	K562	blood:
6	chr2:183220786..183225092-chr2:183225248..183228403,3	MCF-7	breast:
7	chr2:183165658..183166473-chr2:183513729..183514661,3	MCF-7	breast:
8	chr2:183105303..183105848-chr2:183450937..183451448,2	MCF-7	breast:
9	chr2:183220786..183225092-chr2:183225248..183228403,3	MCF-7	breast:
10	chr2:183182727..183184381-chr2:183186031..183187729,2	K562	blood:
11	chr12:82936658..82939200-chr2:183214684..183217154,2	MCF-7	breast:
12	chr2:183139290..183141946-chr2:183155474..183158091,2	K562	blood:
13	chr2:183172864..183175852-chr2:183181543..183183109,2	K562	blood:
14	chr2:183165936..183166478-chr2:183451147..183451888,2	MCF-7	breast:
15	chr2:183103040..183104711-chr2:183106820..183108898,2	K562	blood:
16	chr2:183179551..183180178-chr3:111918314..111918885,2	MCF-7	breast:

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

Variant related genes	Relation type
RN7SL267P	TF binding region
PDE1A	TF binding region
RN7SL267P	CpG island
PDE1A	CpG island

Extended variants
information (count: 5815 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:5815 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79383286	chr2:183067420-183067421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs193085265	chr2:183067427-183067428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536423019	chr2:183067450-183067451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565435114	chr2:183067551-183067552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565798956	chr2:183067606-183067607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184745655	chr2:183067622-183067623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187966072	chr2:183067687-183067688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs578209198	chr2:183067710-183067711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537380162	chr2:183067732-183067733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs180928390	chr2:183067747-183067748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200757950	chr2:183067753-183067754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145912467	chr2:183067766-183067767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373927883	chr2:183067783-183067784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574199898	chr2:183067806-183067807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113409140	chr2:183067814-183067815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553113843	chr2:183067818-183067819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112347667	chr2:183067839-183067840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374324904	chr2:183067869-183067870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75783521	chr2:183067897-183067898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62190461	chr2:183067899-183067900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4666819	chr2:183067972-183067973	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs530508602	chr2:183067986-183067987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201836568	chr2:183068046-183068047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534505982	chr2:183068047-183068048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200051900	chr2:183068050-183068051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201452646	chr2:183068051-183068052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369610867	chr2:183068052-183068053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs367647434	chr2:183068054-183068055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544205483	chr2:183068066-183068067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199535247	chr2:183068067-183068068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200888427	chr2:183068071-183068072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7588289	chr2:183068114-183068115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs374844128	chr2:183068115-183068116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545282926	chr2:183068153-183068154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560139284	chr2:183068158-183068159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183863239	chr2:183068162-183068163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546345359	chr2:183068167-183068168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565860880	chr2:183068175-183068176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376866440	chr2:183068217-183068218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528534168	chr2:183068225-183068226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540227790	chr2:183068226-183068227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551839880	chr2:183068270-183068271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189514643	chr2:183068298-183068299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569921972	chr2:183068322-183068323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17457323	chr2:183068449-183068450	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557410866	chr2:183068450-183068451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111952524	chr2:183068473-183068474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181522716	chr2:183068561-183068562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552055779	chr2:183068581-183068582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553575513	chr2:183068675-183068676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183048400-183073000	Weak transcription	Fetal Stomach	stomach
2	chr2:183061000-183085000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr2:183065000-183067600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:183065800-183087600	Weak transcription	Aorta	Aorta
5	chr2:183065800-183087600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr2:183066000-183068200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr2:183066200-183074800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:183066600-183069800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:183067000-183084000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:183067600-183071200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:183069800-183071600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:183071200-183071600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:183071600-183073200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:183071600-183086800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr2:183072000-183072800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr2:183072000-183072800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr2:183072200-183072400	Enhancers	GM12878-XiMat	blood
18	chr2:183072400-183072800	Enhancers	H1 Cell Line	embryonic stem cell
19	chr2:183072400-183072800	Flanking Active TSS	GM12878-XiMat	blood
20	chr2:183072600-183072800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr2:183072600-183073000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:183072800-183073400	Enhancers	GM12878-XiMat	blood
23	chr2:183072800-183076600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr2:183073000-183073400	Strong transcription	Fetal Stomach	stomach
25	chr2:183073200-183075000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:183073400-183074200	Weak transcription	Fetal Stomach	stomach
27	chr2:183074200-183074600	Strong transcription	Fetal Stomach	stomach
28	chr2:183074600-183076200	Weak transcription	Fetal Stomach	stomach
29	chr2:183074800-183076200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:183075000-183075200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:183075200-183076800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:183076200-183083600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr2:183076800-183083200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:183083200-183085800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:183083600-183083800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:183083800-183086800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:183084000-183086400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:183084200-183084400	Enhancers	Fetal Kidney	kidney
39	chr2:183084200-183085000	Enhancers	Fetal Brain Male	brain
40	chr2:183084200-183086200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr2:183084200-183086200	Enhancers	Brain Germinal Matrix	brain
42	chr2:183084200-183086200	Enhancers	Fetal Brain Female	brain
43	chr2:183084400-183086200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:183084400-183090600	Weak transcription	Fetal Kidney	kidney
45	chr2:183084400-183095200	Weak transcription	Left Ventricle	heart
46	chr2:183084800-183085800	Enhancers	Brain Substantia Nigra	brain
47	chr2:183084800-183086400	Enhancers	Brain Angular Gyrus	brain
48	chr2:183085000-183085400	Enhancers	Brain Cingulate Gyrus	brain
49	chr2:183085000-183085400	Enhancers	Brain Hippocampus Middle	brain
50	chr2:183085000-183085400	Weak transcription	Fetal Brain Male	brain

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