Variant report

Variant	nsv934024
Chromosome Location	chr2:50948700-51079286
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	chr2:50952036-50952291	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr2:51039958-51040191	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:50951993-50952357	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:51003545-51003679	IMR90	lung:	n/a	n/a
6	CEBPB	chr2:51077720-51078095	HepG2	liver:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
7	CEBPB	chr2:50951301-50951586	HepG2	liver:	n/a	chr2:50951423-50951436 chr2:50951424-50951435
8	CEBPB	chr2:51042035-51042364	HepG2	liver:	n/a	chr2:51042175-51042186
9	CEBPB	chr2:51051532-51051664	HepG2	liver:	n/a	chr2:51051618-51051629 chr2:51051616-51051627 chr2:51051616-51051629
10	CEBPB	chr2:50974968-50975018	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:50952000-50952353	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:50954382-50954517	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:51042082-51042350	A549	lung:	n/a	chr2:51042175-51042186
14	CEBPB	chr2:51077765-51078077	A549	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
15	CEBPB	chr2:51077732-51078049	Hela-S3	cervix:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
16	CEBPB	chr2:51077746-51078099	IMR90	lung:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
17	CEBPB	chr2:50952033-50952347	A549	lung:	n/a	n/a
18	CEBPB	chr2:51077727-51078088	H1-hESC	embryonic stem cell:	n/a	chr2:51077903-51077914 chr2:51077818-51077830 chr2:51077904-51077913
19	CEBPB	chr2:51068879-51068992	HepG2	liver:	n/a	chr2:51068958-51068969
20	CHD2	chr2:51020103-51020131	GM12878	blood:	n/a	n/a
21	CTCF	chr2:50973760-50973910	WERI-Rb-1	eye:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
22	CTCF	chr2:50973780-50973930	HRPEpiC	eye:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
23	CTCF	chr2:50973760-50973910	GM12864	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
24	CTCF	chr2:50973760-50973910	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
25	CTCF	chr2:50973752-50973913	GM10248	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
26	CTCF	chr2:50973740-50973890	GM12871	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
27	CTCF	chr2:50973760-50973923	K562	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
28	CTCF	chr2:50973721-50973966	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
29	CTCF	chr2:50973760-50973910	Caco-2	colon:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
30	CTCF	chr2:50973760-50973910	AG09319	gingival:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
31	CTCF	chr2:50973740-50973890	HA-sp	spinal cord:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
32	CTCF	chr2:50973820-50973970	HCM	heart:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
33	CTCF	chr2:50973746-50973953	A549	lung:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
34	CTCF	chr2:50973700-50973850	NHDF-neo	bronchial:	n/a	chr2:50973841-50973849
35	CTCF	chr2:50973740-50973890	SK-N-SH_RA	brain:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
36	CTCF	chr2:50973760-50973910	HPAF	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
37	CTCF	chr2:50973733-50973956	GM13977	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
38	CTCF	chr2:50973720-50973870	HEK293	kidney:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
39	CTCF	chr2:50973642-50974009	HepG2	liver:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
40	CTCF	chr2:51013620-51013770	WERI-Rb-1	eye:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
41	CTCF	chr2:50973760-50973910	GM12875	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
42	CTCF	chr2:51013580-51013730	HRE	kidney:	n/a	chr2:51013673-51013694 chr2:51013679-51013695 chr2:51013678-51013696
43	CTCF	chr2:50973760-50973910	HCFaa	heart:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
44	CTCF	chr2:50973720-50973870	GM12866	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
45	CTCF	chr2:50973705-50973962	Hela-S3	cervix:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
46	CTCF	chr2:50973783-50973941	GM13976	blood:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
47	CTCF	chr2:50973622-50974108	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
48	CTCF	chr2:50973740-50973890	HBMEC	blood vessel:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854
49	CTCF	chr2:50973840-50973990	GM12869	blood:	n/a	chr2:50973841-50973849
50	CTCF	chr2:50973716-50973954	MCF-7	breast:	n/a	chr2:50973838-50973859 chr2:50973841-50973849 chr2:50973836-50973854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50992829-50992879	HCF	heart:	n/a
2	chr2:50992829-50992879	SK-N-MC	brain:	n/a
3	chr2:50956659-50956709	HEEpiC	esophagus:	n/a
4	chr2:51057548-51057598	HMEC	breast:	n/a
5	chr2:50992829-50992879	SAEC	small airway:	n/a
6	chr2:50956659-50956709	BJ	skin:	n/a
7	chr2:51074939-51074989	K562	blood:	n/a
8	chr2:51074939-51074989	H1-hESC	embryonic stem cell:	embryo
9	chr2:51074939-51074989	HepG2	liver:	n/a
10	chr2:50956659-50956709	SAEC	small airway:	n/a
11	chr2:51001003-51001053	NB4	blood:	n/a
12	chr2:50956659-50956709	K562	blood:	n/a
13	chr2:51001003-51001053	NHBE	bronchial:	n/a
14	chr2:50992829-50992879	HCM	heart:	n/a
15	chr2:51001003-51001053	T-47D	breast:	n/a
16	chr2:51057218-51057268	AG04449	skin:	fetal
17	chr2:50992829-50992879	NHBE	bronchial:	n/a
18	chr2:50956659-50956709	SK-N-MC	brain:	n/a
19	chr2:50992829-50992879	NB4	blood:	n/a
20	chr2:50956659-50956709	NH-A	brain:	n/a
21	chr2:51056822-51056872	ProgFib	skin:	n/a
22	chr2:50992829-50992879	HRE	kidney:	n/a
23	chr2:51074881-51074931	A549	lung:	n/a
24	chr2:51057218-51057268	HEK293	kidney:	embryo
25	chr2:51057218-51057268	HNPCEpiC	eye:	n/a
26	chr2:51057218-51057268	CMK	blood:	n/a
27	chr2:51057218-51057268	Hepatocyte	liver:	n/a
28	chr2:50956659-50956709	GM12891	blood:	n/a
29	chr2:51065673-51065723	SAEC	small airway:	n/a
30	chr2:51001003-51001053	RPTEC	kidney:	n/a
31	chr2:51057218-51057268	AG04450	lung:	fetal
32	chr2:51056822-51056872	AG10803	skin:	n/a
33	chr2:51001003-51001053	SK-N-SH	brain:	n/a
34	chr2:51057218-51057268	HRE	kidney:	n/a
35	chr2:51057548-51057598	ECC-1	luminal epithelium:	n/a
36	chr2:51074939-51074989	AG10803	skin:	n/a
37	chr2:50992829-50992879	A549	lung:	n/a
38	chr2:51057548-51057598	HUVEC	blood vessel:	n/a
39	chr2:51074881-51074931	Hela-S3	cervix:	n/a
40	chr2:51001003-51001053	SK-N-MC	brain:	n/a
41	chr2:51057218-51057268	ECC-1	luminal epithelium:	n/a
42	chr2:51074881-51074931	ProgFib	skin:	n/a
43	chr2:51057548-51057598	HAEpiC	amniotic membrane:	n/a
44	chr2:50956659-50956709	A549	lung:	n/a
45	chr2:51056884-51056934	ProgFib	skin:	n/a
46	chr2:51074939-51074989	NH-A	brain:	n/a
47	chr2:51056884-51056934	MCF10A-Er-Src	breast:	n/a
48	chr2:50992829-50992879	IMR90	lung:	fetal
49	chr2:50956659-50956709	BE2_C	brain:	n/a
50	chr2:51001003-51001053	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
2	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
3	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
4	chr2:50977335..50979735-chr2:50992909..50995322,2	K562	blood:
5	chr2:50973459..50974271-chr2:52224493..52225477,4	MCF-7	breast:
6	chr2:51018306..51019906-chr2:51022210..51025087,2	K562	blood:
7	chr2:50985182..50988156-chr2:50995412..50998213,2	K562	blood:
8	chr2:50965713..50967269-chr2:50975937..50978033,2	K562	blood:
9	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
ENSG00000238165	TF binding region
ENSG00000215968	TF binding region
ENSG00000238165	CpG island
ENSG00000215968	CpG island

Extended variants
information (count: 4536 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:4536 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540247571	chr2:50948723-50948724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562446168	chr2:50948731-50948732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150706548	chr2:50948762-50948763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182181425	chr2:50948776-50948777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544463357	chr2:50948796-50948797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373799223	chr2:50948825-50948826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533323056	chr2:50948867-50948868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551090493	chr2:50948967-50948968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559802480	chr2:50949087-50949088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368093842	chr2:50949106-50949107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548701251	chr2:50949141-50949142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187590337	chr2:50949184-50949185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537756901	chr2:50949223-50949224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190324760	chr2:50949239-50949240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550063510	chr2:50949246-50949247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142496197	chr2:50949250-50949251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181058384	chr2:50949270-50949271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558317285	chr2:50949332-50949333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185069655	chr2:50949333-50949334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190126053	chr2:50949335-50949336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182398149	chr2:50949374-50949375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185939700	chr2:50949398-50949399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573944095	chr2:50949477-50949478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145968402	chr2:50949485-50949486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556418777	chr2:50949507-50949508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577852719	chr2:50949508-50949509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537048224	chr2:50949522-50949523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545189386	chr2:50949558-50949559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139932941	chr2:50949589-50949590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527400166	chr2:50949601-50949602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542664484	chr2:50949603-50949604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560734168	chr2:50949608-50949609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531302701	chr2:50949615-50949616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114092655	chr2:50949620-50949621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571549060	chr2:50949692-50949693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532387380	chr2:50949756-50949757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191734088	chr2:50949770-50949771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183329028	chr2:50949798-50949799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555583176	chr2:50949817-50949818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534237788	chr2:50949856-50949857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111234963	chr2:50949858-50949859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374749275	chr2:50949895-50949896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189182641	chr2:50949901-50949902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368935387	chr2:50949914-50949915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191930045	chr2:50949919-50949920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537834247	chr2:50949927-50949928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556481178	chr2:50949966-50949967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372959557	chr2:50950024-50950025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556650183	chr2:50950032-50950033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370653285	chr2:50950087-50950088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Autism	20841430	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50947000-50948800	Enhancers	Brain Angular Gyrus	brain
2	chr2:50947400-50948800	Enhancers	Brain Germinal Matrix	brain
3	chr2:50947600-50948800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr2:50947600-50948800	Enhancers	Brain Hippocampus Middle	brain
5	chr2:50947600-50948800	Enhancers	Fetal Brain Female	brain
6	chr2:50947600-50950800	Weak transcription	Fetal Kidney	kidney
7	chr2:50947800-50949800	Weak transcription	Brain Substantia Nigra	brain
8	chr2:50948000-50948800	Enhancers	Brain Anterior Caudate	brain
9	chr2:50948200-50950000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr2:50948400-50950000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr2:50948400-50950000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:50948400-50950000	Weak transcription	Fetal Muscle Leg	muscle
13	chr2:50948400-50950200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:50948400-50957000	Weak transcription	Fetal Brain Male	brain
15	chr2:50948600-50949800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr2:50948600-50949800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr2:50948600-50949800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr2:50948600-50950000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:50948600-50950000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr2:50948600-50950000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr2:50948600-50950200	Weak transcription	Fetal Stomach	stomach
22	chr2:50948600-50950800	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr2:50948600-50956400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr2:50948600-50956600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:50948600-50956600	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr2:50948800-50949800	Weak transcription	Brain Hippocampus Middle	brain
27	chr2:50948800-50950000	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr2:50948800-50950200	Weak transcription	Brain Anterior Caudate	brain
29	chr2:50948800-50950600	Weak transcription	Brain Angular Gyrus	brain
30	chr2:50948800-50954800	Weak transcription	Brain Germinal Matrix	brain
31	chr2:50948800-50955200	Weak transcription	Fetal Brain Female	brain
32	chr2:50949800-50950000	Enhancers	Brain Hippocampus Middle	brain
33	chr2:50949800-50951200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:50949800-50951200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr2:50949800-50951200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr2:50949800-50951200	Enhancers	Colon Smooth Muscle	Colon
37	chr2:50949800-50951400	Enhancers	Brain Substantia Nigra	brain
38	chr2:50949800-50952200	Enhancers	Rectal Smooth Muscle	rectum
39	chr2:50950000-50950200	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:50950000-50950400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:50950000-50950400	Weak transcription	Brain Hippocampus Middle	brain
42	chr2:50950000-50950800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr2:50950000-50951000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr2:50950000-50951000	Enhancers	Fetal Muscle Leg	muscle
45	chr2:50950000-50951200	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr2:50950000-50951800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr2:50950000-50952000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:50950200-50950600	Weak transcription	Brain Cingulate Gyrus	brain
49	chr2:50950200-50951000	Enhancers	Fetal Stomach	stomach
50	chr2:50950200-50951200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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