Variant report

Variant	nsv1012150
Chromosome Location	chr2:53788495-53840009
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	BHLHE40	chr2:53788428-53788646	HepG2	liver:	n/a	n/a
2	BRCA1	chr2:53789639-53789689	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr2:53824394-53824714	HepG2	liver:	n/a	chr2:53824617-53824628 chr2:53824562-53824573 chr2:53824621-53824632 chr2:53824524-53824535 chr2:53824621-53824632
4	CEBPB	chr2:53832665-53832917	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr2:53789634-53789824	HepG2	liver:	n/a	chr2:53789749-53789760
6	CEBPB	chr2:53804310-53804615	K562	blood:	n/a	chr2:53804453-53804464
7	CEBPB	chr2:53789584-53789940	A549	lung:	n/a	chr2:53789749-53789760
8	CEBPB	chr2:53837658-53837919	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:53795619-53795883	MCF-7	breast:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
10	CEBPB	chr2:53795638-53795866	K562	blood:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
11	CEBPB	chr2:53789566-53789937	HepG2	liver:	n/a	chr2:53789749-53789760
12	CEBPB	chr2:53789454-53789990	MCF-7	breast:	n/a	chr2:53789749-53789760
13	CEBPB	chr2:53789530-53789931	MCF-7	breast:	n/a	chr2:53789749-53789760
14	CEBPB	chr2:53795612-53795942	HepG2	liver:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
15	CEBPB	chr2:53804321-53804582	IMR90	lung:	n/a	chr2:53804453-53804464
16	CEBPB	chr2:53789586-53789943	K562	blood:	n/a	chr2:53789749-53789760
17	CEBPB	chr2:53795600-53796008	A549	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
18	CEBPB	chr2:53789569-53789929	IMR90	lung:	n/a	chr2:53789749-53789760
19	CEBPB	chr2:53824449-53824637	Hela-S3	cervix:	n/a	chr2:53824617-53824628 chr2:53824562-53824573 chr2:53824621-53824632 chr2:53824524-53824535 chr2:53824621-53824632
20	CEBPB	chr2:53795589-53795907	ECC-1	luminal epithelium:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
21	CEBPB	chr2:53789661-53789917	H1-hESC	embryonic stem cell:	n/a	chr2:53789749-53789760
22	CEBPB	chr2:53810690-53810961	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:53795595-53795940	Hela-S3	cervix:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
24	CEBPB	chr2:53795596-53795941	A549	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
25	CEBPB	chr2:53789527-53789962	Hela-S3	cervix:	n/a	chr2:53789749-53789760
26	CEBPB	chr2:53821343-53821832	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:53804303-53804543	HepG2	liver:	n/a	chr2:53804453-53804464
28	CEBPB	chr2:53789525-53790053	A549	lung:	n/a	chr2:53789749-53789760
29	CEBPB	chr2:53789476-53789920	HCT-116	colon:	n/a	chr2:53789749-53789760
30	CEBPB	chr2:53795617-53795967	ECC-1	luminal epithelium:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
31	CEBPB	chr2:53789571-53789923	ECC-1	luminal epithelium:	n/a	chr2:53789749-53789760
32	CEBPB	chr2:53795583-53795925	IMR90	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
33	CHD2	chr2:53789582-53789771	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr2:53797250-53797323	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:53808660-53808810	WI-38	lung:	n/a	n/a
36	CTCF	chr2:53797240-53797390	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr2:53797127-53797398	K562	blood:	n/a	n/a
38	CTCF	chr2:53797211-53797367	HepG2	liver:	n/a	n/a
39	CTCF	chr2:53797240-53797390	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr2:53836820-53836970	SAEC	small airway:	n/a	n/a
41	CTCF	chr2:53797233-53797350	HepG2	liver:	n/a	n/a
42	CTCF	chr2:53797220-53797370	HMEC	breast:	n/a	n/a
43	CTCF	chr2:53825901-53825930	GM20000	blood:	n/a	n/a
44	CTCF	chr2:53797120-53797270	BE2_C	brain:	n/a	n/a
45	CTCF	chr2:53797200-53797350	Caco-2	colon:	n/a	n/a
46	CTCF	chr2:53797233-53797348	Gliobla	brain:	n/a	n/a
47	CTCF	chr2:53833903-53833938	Lung_OC	lung:	n/a	n/a
48	CTCF	chr2:53821681-53821773	Fibrobl	skin:	n/a	n/a
49	CTCF	chr2:53797216-53797349	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:53797290-53797311	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53803878-53803928	HRPEpiC	eye:	n/a
2	chr2:53803878-53803928	HMEC	breast:	n/a
3	chr2:53803878-53803928	Hepatocyte	liver:	n/a
4	chr2:53803878-53803928	T-47D	breast:	n/a
5	chr2:53814537-53814587	NH-A	brain:	n/a
6	chr2:53803878-53803928	GM12891	blood:	n/a
7	chr2:53803878-53803928	BJ	skin:	n/a
8	chr2:53814261-53814311	HepG2	liver:	n/a
9	chr2:53803878-53803928	HCM	heart:	n/a
10	chr2:53814537-53814587	U87	brain:	n/a
11	chr2:53814261-53814311	HRE	kidney:	n/a
12	chr2:53803878-53803928	Jurkat	blood:	n/a
13	chr2:53814261-53814311	K562	blood:	n/a
14	chr2:53814537-53814587	AG10803	skin:	n/a
15	chr2:53803878-53803928	GM19239	blood:	n/a
16	chr2:53814537-53814587	Caco-2	colon:	n/a
17	chr2:53803878-53803928	NHDF-neo	bronchial:	n/a
18	chr2:53803878-53803928	GM12878	blood:	n/a
19	chr2:53803878-53803928	AG04449	skin:	fetal
20	chr2:53803878-53803928	HCPEpiC	choroid plexus:	n/a
21	chr2:53814261-53814311	NH-A	brain:	n/a
22	chr2:53814537-53814587	K562	blood:	n/a
23	chr2:53803878-53803928	NT2-D1	testis:	n/a
24	chr2:53814261-53814311	AG04450	lung:	fetal
25	chr2:53814537-53814587	CMK	blood:	n/a
26	chr2:53814537-53814587	Hela-S3	cervix:	n/a
27	chr2:53814537-53814587	AG04450	lung:	fetal
28	chr2:53803878-53803928	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:53814537-53814587	LNCaP	prostate:	n/a
30	chr2:53814537-53814587	MCF10A-Er-Src	breast:	n/a
31	chr2:53814537-53814587	HCPEpiC	choroid plexus:	n/a
32	chr2:53803878-53803928	HUVEC	blood vessel:	n/a
33	chr2:53814261-53814311	HEK293	kidney:	embryo
34	chr2:53803878-53803928	PANC-1	pancreas:	n/a
35	chr2:53803878-53803928	GM12892	blood:	n/a
36	chr2:53814261-53814311	NB4	blood:	n/a
37	chr2:53803878-53803928	NH-A	brain:	n/a
38	chr2:53814537-53814587	H1-hESC	embryonic stem cell:	embryo
39	chr2:53814261-53814311	HRPEpiC	eye:	n/a
40	chr2:53814537-53814587	HAEpiC	amniotic membrane:	n/a
41	chr2:53803878-53803928	HRCEpiC	kidney:	n/a
42	chr2:53814537-53814587	GM12891	blood:	n/a
43	chr2:53814261-53814311	HAEpiC	amniotic membrane:	n/a
44	chr2:53814537-53814587	AG09319	gingival:	n/a
45	chr2:53814261-53814311	HCM	heart:	n/a
46	chr2:53803878-53803928	HCF	heart:	n/a
47	chr2:53814261-53814311	HCT-116	colon:	n/a
48	chr2:53814537-53814587	HEEpiC	esophagus:	n/a
49	chr2:53814261-53814311	HRCEpiC	kidney:	n/a
50	chr2:53814537-53814587	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:53807910..53809861-chr2:53812392..53815157,2	K562	blood:
2	chr2:53804711..53806458-chr2:53809800..53812091,2	MCF-7	breast:
3	chr2:53807910..53809861-chr2:53812392..53815157,2	K562	blood:
4	chr2:53804711..53806458-chr2:53809800..53812091,2	MCF-7	breast:
5	chr2:53800207..53803097-chr2:53806024..53807990,2	K562	blood:
6	chr2:53838050..53841676-chr2:53842441..53845129,3	K562	blood:
7	chr2:53791197..53793053-chr2:53794870..53797027,2	K562	blood:
8	chr2:53795938..53798218-chr2:53812190..53814681,2	K562	blood:
9	chr2:53802111..53805957-chr2:53807457..53810844,3	K562	blood:
10	chr2:53837091..53839319-chr2:53840310..53842800,2	K562	blood:
11	chr2:53791197..53793053-chr2:53794870..53797027,2	K562	blood:
12	chr2:53800207..53803097-chr2:53806024..53807990,2	K562	blood:
13	chr2:53796597..53798405-chr2:53800976..53803366,2	MCF-7	breast:
14	chr2:53802111..53805957-chr2:53807457..53810844,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR75-6	chr2:53833057-53833215	NONHSAT070689
2	lnc-GPR75-6	chr2:53808341-53808515	NONHSAT070689
3	lnc-GPR75-6	chr2:53833057-53833217	NONHSAT070690
4	lnc-GPR75-6	chr2:53830522-53830655	NONHSAT070689
5	lnc-GPR75-6	chr2:53833559-53833596	NONHSAT070690
6	lnc-GPR75-6	chr2:53831411-53831558	NONHSAT070689
7	lnc-GPR75-6	chr2:53831784-53832052	NONHSAT070690
8	lnc-GPR75-6	chr2:53831895-53832052	NONHSAT070689

Variant related genes	Relation type
RNU6-997P	TF binding region
GPR75-ASB3	TF binding region
RNU6-997P	CpG island
GPR75-ASB3	CpG island
ENSG00000207456	chromatin interactions

Extended variants
information (count: 1792 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1792 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577965368	chr2:53788496-53788497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186515069	chr2:53788536-53788537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7609417	chr2:53788542-53788543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375472464	chr2:53788661-53788662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540571299	chr2:53788665-53788666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540342174	chr2:53788669-53788670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7609437	chr2:53788673-53788674	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs72895290	chr2:53788687-53788688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543235948	chr2:53788727-53788728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191461717	chr2:53788753-53788754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532070560	chr2:53788788-53788789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529527178	chr2:53788841-53788842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs151166641	chr2:53788845-53788846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564938317	chr2:53788861-53788862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527738821	chr2:53788890-53788891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180690055	chr2:53788894-53788895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547501206	chr2:53788912-53788913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566301041	chr2:53788924-53788925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533749000	chr2:53788952-53788953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529055227	chr2:53788955-53788956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141954832	chr2:53789027-53789028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569055282	chr2:53789101-53789102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145819392	chr2:53789108-53789109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563048513	chr2:53789119-53789120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11889309	chr2:53789146-53789147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550642010	chr2:53789193-53789194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571282374	chr2:53789245-53789246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12053268	chr2:53789256-53789257	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553883016	chr2:53789276-53789277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371638737	chr2:53789285-53789286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573717006	chr2:53789310-53789311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368156584	chr2:53789341-53789342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542840995	chr2:53789365-53789366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35311904	chr2:53789426-53789427	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs374103188	chr2:53789438-53789439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546500907	chr2:53789443-53789444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185168656	chr2:53789505-53789506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545691505	chr2:53789522-53789523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564900813	chr2:53789600-53789601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138883111	chr2:53789622-53789623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190769141	chr2:53789682-53789683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561038212	chr2:53789710-53789711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566398398	chr2:53789717-53789718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530261682	chr2:53789754-53789755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140399325	chr2:53789755-53789756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113802727	chr2:53789772-53789773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531474639	chr2:53789792-53789793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs59628333	chr2:53789793-53789794	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs76487690	chr2:53789842-53789843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79483228	chr2:53789895-53789896	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	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
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53787400-53789200	Weak transcription	Hela-S3	cervix
2	chr2:53788200-53788800	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr2:53789200-53789600	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr2:53789200-53789800	Enhancers	Hela-S3	cervix
5	chr2:53789200-53790000	Enhancers	Brain Hippocampus Middle	brain
6	chr2:53789200-53790000	Enhancers	Brain Substantia Nigra	brain
7	chr2:53789400-53789800	Enhancers	Brain Cingulate Gyrus	brain
8	chr2:53789400-53790000	Enhancers	Placenta	Placenta
9	chr2:53790400-53791000	Enhancers	Colon Smooth Muscle	Colon
10	chr2:53790600-53791200	Enhancers	Rectal Smooth Muscle	rectum
11	chr2:53791000-53792400	Weak transcription	Colon Smooth Muscle	Colon
12	chr2:53792400-53792600	Enhancers	Colon Smooth Muscle	Colon
13	chr2:53794000-53794600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:53794200-53795000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:53795000-53808800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:53795200-53796200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr2:53795600-53795800	Active TSS	Dnd41	blood
18	chr2:53795600-53796000	Active TSS	Brain Substantia Nigra	brain
19	chr2:53795600-53796200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:53795600-53796200	Active TSS	Aorta	Aorta
21	chr2:53795600-53796200	Enhancers	Brain Anterior Caudate	brain
22	chr2:53795600-53796200	Active TSS	A549	lung
23	chr2:53795600-53796200	Active TSS	Osteobl	bone
24	chr2:53795600-53797400	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr2:53795800-53796000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr2:53795800-53796000	Enhancers	Fetal Muscle Leg	muscle
27	chr2:53795800-53796000	Flanking Active TSS	Dnd41	blood
28	chr2:53795800-53796200	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr2:53795800-53796400	Enhancers	Brain Hippocampus Middle	brain
30	chr2:53796000-53796200	Enhancers	Brain Substantia Nigra	brain
31	chr2:53796200-53799000	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr2:53796200-53799000	Weak transcription	Brain Substantia Nigra	brain
33	chr2:53796200-53802800	Weak transcription	Brain Anterior Caudate	brain
34	chr2:53796400-53799200	Weak transcription	Brain Hippocampus Middle	brain
35	chr2:53797200-53798200	Enhancers	Pancreas	Pancrea
36	chr2:53797400-53797800	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr2:53799000-53799400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:53799000-53799800	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr2:53799000-53800400	Enhancers	Brain Substantia Nigra	brain
40	chr2:53799200-53800000	Enhancers	Brain Cingulate Gyrus	brain
41	chr2:53799200-53800200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:53799200-53800200	Enhancers	Brain Hippocampus Middle	brain
43	chr2:53799400-53802600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:53799600-53800000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr2:53799800-53801800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr2:53800200-53803000	Weak transcription	Brain Hippocampus Middle	brain
47	chr2:53801800-53804400	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr2:53802200-53804400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:53802400-53804200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr2:53802600-53802800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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