Variant report

Variant	nsv874045
Chromosome Location	chr2:50924358-51073449
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	BACH1	chr2:50955596-50955702	K562	blood:	n/a	n/a
2	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
3	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
5	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
6	CEBPB	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
8	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
10	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
15	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
16	CHD2	chr2:50947884-50948198	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr2:50973780-50973930	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
18	CTCF	chr2:50973760-50973910	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
19	CTCF	chr2:50973554-50974218	SK-N-SH	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
20	CTCF	chr2:50973740-50973890	HAc	cerebellar:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
21	CTCF	chr2:50973760-50973910	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
22	CTCF	chr2:50973800-50973950	GM06990	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:51013580-51013730	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
24	CTCF	chr2:50973760-50973910	RPTEC	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:51013675-51013707	K562	blood:	n/a	chr2:51013679-51013695 chr2:51013678-51013696
26	CTCF	chr2:50973420-50973570	HAc	cerebellar:	n/a	n/a
27	CTCF	chr2:50973746-50973953	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973780-50973930	HCM	heart:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973800-50973950	HL-60	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973738-50973944	Medullo	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:51013578-51013819	Medullo	brain:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
32	CTCF	chr2:50973760-50973910	BE2_C	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:51009720-51009870	AG04450	lung:	n/a	chr2:51009841-51009854
34	CTCF	chr2:50973800-50973950	GM12870	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
35	CTCF	chr2:50973729-50973949	NHEK	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973760-50973910	BJ	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973760-50973910	HPAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973783-50973941	GM13976	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973740-50973890	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:50973760-50973910	HA-sp	spinal cord:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
41	CTCF	chr2:50973780-50973930	HCPEpiC	choroid plexus:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:50973620-50973770	A549	lung:	n/a	n/a
43	CTCF	chr2:50973687-50973983	Gliobla	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973740-50973890	NB4	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973747-50973915	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973800-50973950	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973733-50973949	ProgFib	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973780-50973930	HUVEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973733-50973905	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
50	CTCF	chr2:50973760-50973910	AG04449	skin:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
2	chr2:51056884-51056934	GM19239	blood:	n/a
3	chr2:50956659-50956709	NHDF-neo	bronchial:	n/a
4	chr2:51056884-51056934	GM19239	blood:	n/a
5	chr2:50992829-50992879	HCT-116	colon:	n/a
6	chr2:50992829-50992879	MCF10A-Er-Src	breast:	n/a
7	chr2:51056822-51056872	ECC-1	luminal epithelium:	n/a
8	chr2:50992829-50992879	PFSK-1	brain:	n/a
9	chr2:50992829-50992879	HRCEpiC	kidney:	n/a
10	chr2:50956659-50956709	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:50956659-50956709	HIPEpiC	eye:	n/a
12	chr2:51056884-51056934	K562	blood:	n/a
13	chr2:51056822-51056872	Jurkat	blood:	n/a
14	chr2:51056822-51056872	SK-N-MC	brain:	n/a
15	chr2:50956659-50956709	SKMC	muscle:	n/a
16	chr2:51056884-51056934	IMR90	lung:	fetal
17	chr2:51057218-51057268	A549	lung:	n/a
18	chr2:51056822-51056872	NH-A	brain:	n/a
19	chr2:51001003-51001053	HRE	kidney:	n/a
20	chr2:51056822-51056872	BJ	skin:	n/a
21	chr2:51001003-51001053	GM12891	blood:	n/a
22	chr2:51056822-51056872	HCM	heart:	n/a
23	chr2:51001003-51001053	HUVEC	blood vessel:	n/a
24	chr2:51065673-51065723	HIPEpiC	eye:	n/a
25	chr2:51065673-51065723	Hepatocyte	liver:	n/a
26	chr2:50956659-50956709	NT2-D1	testis:	n/a
27	chr2:51056884-51056934	SKMC	muscle:	n/a
28	chr2:51057548-51057598	HCF	heart:	n/a
29	chr2:51001003-51001053	SK-N-SH	brain:	n/a
30	chr2:51056884-51056934	HEEpiC	esophagus:	n/a
31	chr2:51056884-51056934	HCT-116	colon:	n/a
32	chr2:50992829-50992879	HRPEpiC	eye:	n/a
33	chr2:51056822-51056872	GM12891	blood:	n/a
34	chr2:51065673-51065723	HL-60	blood:	n/a
35	chr2:50956659-50956709	MCF10A-Er-Src	breast:	n/a
36	chr2:51056884-51056934	PFSK-1	brain:	n/a
37	chr2:51056822-51056872	NT2-D1	testis:	n/a
38	chr2:50956659-50956709	ProgFib	skin:	n/a
39	chr2:51057548-51057598	RPTEC	kidney:	n/a
40	chr2:51056822-51056872	A549	lung:	n/a
41	chr2:51057548-51057598	SK-N-SH_RA	brain:	n/a
42	chr2:51057218-51057268	NHBE	bronchial:	n/a
43	chr2:51056822-51056872	PFSK-1	brain:	n/a
44	chr2:51065673-51065723	IMR90	lung:	fetal
45	chr2:51056884-51056934	ProgFib	skin:	n/a
46	chr2:51057548-51057598	HAEpiC	amniotic membrane:	n/a
47	chr2:51001003-51001053	AG09319	gingival:	n/a
48	chr2:50992829-50992879	ProgFib	skin:	n/a
49	chr2:51057548-51057598	NHBE	bronchial:	n/a
50	chr2:51065673-51065723	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
4	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
5	chr2:50946676..50947176-chr20:60981159..60981778,2	MCF-7	breast:
6	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
7	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
8	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
9	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
10	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSHR-5	chr2:51056580-51056816	NONHSAT070648

Variant related genes	Relation type
ENSG00000216191	TF binding region
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000216191	CpG island
ENSG00000238165	CpG island
ENSG00000215968	CpG island

Extended variants
information (count: 5292 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:5292 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17560229	chr2:50924358-50924359	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191427373	chr2:50924366-50924367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182798054	chr2:50924380-50924381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531426204	chr2:50924417-50924418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187424186	chr2:50924419-50924420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563004361	chr2:50924439-50924440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191967757	chr2:50924501-50924502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184260912	chr2:50924511-50924512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79618071	chr2:50924515-50924516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552596891	chr2:50924516-50924517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527644362	chr2:50924522-50924523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549414968	chr2:50924558-50924559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113582709	chr2:50924603-50924604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571181450	chr2:50924615-50924616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538072664	chr2:50924633-50924634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146593438	chr2:50924646-50924647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527335839	chr2:50924705-50924706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538347015	chr2:50924719-50924720	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs377304677	chr2:50924765-50924766	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs553394968	chr2:50924793-50924794	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs571946586	chr2:50924804-50924805	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536212920	chr2:50924829-50924830	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs554581995	chr2:50924841-50924842	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs576269300	chr2:50924877-50924878	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs187886273	chr2:50924879-50924880	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs575853181	chr2:50924884-50924885	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs547466715	chr2:50924913-50924914	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs193081242	chr2:50924931-50924932	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs578173201	chr2:50924939-50924940	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567047517	chr2:50924953-50924954	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs544852007	chr2:50924958-50924959	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs558159271	chr2:50925057-50925058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140124227	chr2:50925123-50925124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527707484	chr2:50925239-50925240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576477650	chr2:50925250-50925251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549325654	chr2:50925257-50925258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561460319	chr2:50925286-50925287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531864619	chr2:50925296-50925297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550010638	chr2:50925297-50925298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373875876	chr2:50925322-50925323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184492643	chr2:50925368-50925369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545373656	chr2:50925378-50925379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189016943	chr2:50925384-50925385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375420210	chr2:50925404-50925405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs57489293	chr2:50925413-50925414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs559056637	chr2:50925453-50925454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145854475	chr2:50925456-50925457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369526785	chr2:50925467-50925468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535901938	chr2:50925469-50925470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528141003	chr2:50925479-50925480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
small cell lung cancer	20016488	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
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	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
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Acute myeloid leukemia	20729466	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50916000-50948000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:50919200-50929200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr2:50924200-50924800	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr2:50924800-50929800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr2:50929000-50929200	Enhancers	Brain Hippocampus Middle	brain
6	chr2:50929200-50929600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:50929200-50930000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr2:50929200-50930400	Weak transcription	Brain Hippocampus Middle	brain
9	chr2:50929400-50929800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:50929600-50930400	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr2:50929800-50930800	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr2:50930000-50935400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr2:50930400-50930800	Enhancers	Brain Hippocampus Middle	brain
14	chr2:50930400-50934400	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr2:50930800-50941400	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr2:50934200-50935000	Enhancers	Brain Substantia Nigra	brain
17	chr2:50934400-50935000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr2:50934400-50935000	Enhancers	Brain Germinal Matrix	brain
19	chr2:50934600-50935000	Enhancers	Fetal Brain Male	brain
20	chr2:50934800-50935000	Enhancers	Brain Anterior Caudate	brain
21	chr2:50935000-50936000	Weak transcription	Brain Anterior Caudate	brain
22	chr2:50935000-50939800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr2:50935000-50947400	Weak transcription	Fetal Brain Male	brain
24	chr2:50935400-50935800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr2:50935400-50936000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr2:50936000-50936400	Enhancers	Brain Anterior Caudate	brain
27	chr2:50936000-50936400	Enhancers	Pancreas	Pancrea
28	chr2:50937200-50940600	Enhancers	Liver	Liver
29	chr2:50939600-50939800	Enhancers	Fetal Brain Female	brain
30	chr2:50939800-50942000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr2:50939800-50947600	Weak transcription	Fetal Brain Female	brain
32	chr2:50940600-50944800	Weak transcription	Liver	Liver
33	chr2:50941000-50942000	Enhancers	Fetal Kidney	kidney
34	chr2:50941400-50942000	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr2:50941600-50945600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr2:50942000-50943200	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr2:50942000-50947000	Weak transcription	Fetal Kidney	kidney
38	chr2:50942000-50947600	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr2:50943200-50944400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr2:50944400-50946800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr2:50944800-50945400	Enhancers	Liver	Liver
42	chr2:50945400-50945600	Enhancers	Brain Substantia Nigra	brain
43	chr2:50945400-50945800	Enhancers	Brain Hippocampus Middle	brain
44	chr2:50945400-50946600	Weak transcription	Liver	Liver
45	chr2:50945600-50946000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr2:50945600-50947400	Weak transcription	Brain Substantia Nigra	brain
47	chr2:50945800-50946000	Enhancers	Brain Anterior Caudate	brain
48	chr2:50945800-50947600	Weak transcription	Brain Hippocampus Middle	brain
49	chr2:50946000-50947200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr2:50946000-50948000	Weak transcription	Brain Anterior Caudate	brain

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