Variant report

Variant	nsv874034
Chromosome Location	chr2:50855012-50921327
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:211)
CpG islands
(count:245)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
2	CEBPB	chr2:50858684-50858994	HepG2	liver:	n/a	chr2:50858808-50858817 chr2:50858807-50858818 chr2:50858808-50858817 chr2:50858808-50858817 chr2:50858806-50858817 chr2:50858808-50858817
3	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
4	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
5	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
6	CTCF	chr2:50902138-50902315	NHEK	skin:	n/a	n/a
7	CTCF	chr2:50902100-50902250	HFF-Myc	foreskin:	n/a	n/a
8	CTCF	chr2:50902171-50902279	K562	blood:	n/a	n/a
9	CTCF	chr2:50902100-50902250	GM12874	blood:	n/a	n/a
10	CTCF	chr2:50901960-50902110	RPTEC	kidney:	n/a	n/a
11	CTCF	chr2:50902080-50902230	GM12864	blood:	n/a	n/a
12	CTCF	chr2:50902100-50902250	SAEC	small airway:	n/a	n/a
13	CTCF	chr2:50902180-50902330	HA-sp	spinal cord:	n/a	n/a
14	CTCF	chr2:50902035-50902240	K562	blood:	n/a	n/a
15	CTCF	chr2:50902081-50902284	HepG2	liver:	n/a	n/a
16	CTCF	chr2:50902200-50902350	HRE	kidney:	n/a	n/a
17	CTCF	chr2:50902119-50902292	GM19240	blood:	n/a	n/a
18	CTCF	chr2:50906100-50906250	GM12864	blood:	n/a	n/a
19	CTCF	chr2:50902140-50902290	GM12872	blood:	n/a	n/a
20	CTCF	chr2:50902001-50902362	HepG2	liver:	n/a	n/a
21	CTCF	chr2:50902124-50902313	A549	lung:	n/a	n/a
22	CTCF	chr2:50902155-50902320	GM12878	blood:	n/a	n/a
23	CTCF	chr2:50902140-50902290	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr2:50902080-50902230	GM12875	blood:	n/a	n/a
25	CTCF	chr2:50889603-50889665	GM19240	blood:	n/a	n/a
26	CTCF	chr2:50902076-50902365	GM12878	blood:	n/a	n/a
27	CTCF	chr2:50902140-50902290	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr2:50902100-50902250	GM12872	blood:	n/a	n/a
29	CTCF	chr2:50902120-50902270	GM12867	blood:	n/a	n/a
30	CTCF	chr2:50902140-50902290	GM12871	blood:	n/a	n/a
31	CTCF	chr2:50902100-50902250	GM12873	blood:	n/a	n/a
32	CTCF	chr2:50902106-50902258	A549	lung:	n/a	n/a
33	CTCF	chr2:50902182-50902235	LNCaP	prostate:	n/a	n/a
34	CTCF	chr2:50902180-50902330	GM12871	blood:	n/a	n/a
35	CTCF	chr2:50902100-50902250	GM12865	blood:	n/a	n/a
36	CTCF	chr2:50889579-50889662	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:50902128-50902354	IMR90	lung:	n/a	n/a
38	CTCF	chr2:50902080-50902230	HL-60	blood:	n/a	n/a
39	CTCF	chr2:50902120-50902270	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:50902140-50902290	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr2:50902080-50902230	GM12869	blood:	n/a	n/a
42	CTCF	chr2:50902180-50902330	GM12878	blood:	n/a	n/a
43	CTCF	chr2:50889588-50889678	GM19239	blood:	n/a	n/a
44	CTCF	chr2:50902100-50902250	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr2:50902197-50902266	Medullo	brain:	n/a	n/a
46	CTCF	chr2:50902189-50902272	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:50902200-50902350	GM12869	blood:	n/a	n/a
48	CTCF	chr2:50902155-50902284	GM13977	blood:	n/a	n/a
49	CTCF	chr2:50902100-50902250	BE2_C	brain:	n/a	n/a
50	CTCF	chr2:50902154-50902311	Hela-S3	cervix:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50884693-50884743	ECC-1	luminal epithelium:	n/a
2	chr2:50884693-50884743	ECC-1	luminal epithelium:	n/a
3	chr2:50876837-50876887	SK-N-SH	brain:	n/a
4	chr2:50884252-50884302	Hepatocyte	liver:	n/a
5	chr2:50884693-50884743	HRE	kidney:	n/a
6	chr2:50884252-50884302	NH-A	brain:	n/a
7	chr2:50884252-50884302	HUVEC	blood vessel:	n/a
8	chr2:50884252-50884302	GM19239	blood:	n/a
9	chr2:50884693-50884743	HL-60	blood:	n/a
10	chr2:50884693-50884743	HAEpiC	amniotic membrane:	n/a
11	chr2:50863603-50863653	PANC-1	pancreas:	n/a
12	chr2:50884693-50884743	HNPCEpiC	eye:	n/a
13	chr2:50876837-50876887	PANC-1	pancreas:	n/a
14	chr2:50863603-50863653	HUVEC	blood vessel:	n/a
15	chr2:50884693-50884743	LNCaP	prostate:	n/a
16	chr2:50884693-50884743	GM19239	blood:	n/a
17	chr2:50876837-50876887	Hela-S3	cervix:	n/a
18	chr2:50876837-50876887	HUVEC	blood vessel:	n/a
19	chr2:50863603-50863653	HEK293	kidney:	embryo
20	chr2:50863603-50863653	U87	brain:	n/a
21	chr2:50884252-50884302	HCT-116	colon:	n/a
22	chr2:50876837-50876887	HEK293	kidney:	embryo
23	chr2:50884252-50884302	HEK293	kidney:	embryo
24	chr2:50884693-50884743	SKMC	muscle:	n/a
25	chr2:50876837-50876887	SKMC	muscle:	n/a
26	chr2:50876837-50876887	Caco-2	colon:	n/a
27	chr2:50884693-50884743	BJ	skin:	n/a
28	chr2:50884252-50884302	PrEC	prostate:	n/a
29	chr2:50863603-50863653	PrEC	prostate:	n/a
30	chr2:50863603-50863653	AoSMC	blood vessel:	n/a
31	chr2:50884252-50884302	RPTEC	kidney:	n/a
32	chr2:50884693-50884743	Jurkat	blood:	n/a
33	chr2:50876837-50876887	HRPEpiC	eye:	n/a
34	chr2:50876837-50876887	BE2_C	brain:	n/a
35	chr2:50863603-50863653	BE2_C	brain:	n/a
36	chr2:50884252-50884302	HAEpiC	amniotic membrane:	n/a
37	chr2:50876837-50876887	GM06990	blood:	n/a
38	chr2:50876837-50876887	GM12892	blood:	n/a
39	chr2:50884252-50884302	HL-60	blood:	n/a
40	chr2:50876837-50876887	ECC-1	luminal epithelium:	n/a
41	chr2:50884252-50884302	AG09319	gingival:	n/a
42	chr2:50876837-50876887	HRCEpiC	kidney:	n/a
43	chr2:50884252-50884302	PFSK-1	brain:	n/a
44	chr2:50884693-50884743	NB4	blood:	n/a
45	chr2:50884693-50884743	HepG2	liver:	n/a
46	chr2:50863603-50863653	HCPEpiC	choroid plexus:	n/a
47	chr2:50863603-50863653	HCM	heart:	n/a
48	chr2:50884693-50884743	AG10803	skin:	n/a
49	chr2:50863603-50863653	ProgFib	skin:	n/a
50	chr2:50884693-50884743	HEEpiC	esophagus:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:50883231..50884999-chr2:50887642..50889397,2	MCF-7	breast:
2	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
3	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
4	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
5	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
6	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STON1-GTF2A1L-4	chr2:50859486-50859749	NONHSAT070645
2	lnc-STON1-GTF2A1L-4	chr2:50858415-50858521	NONHSAT070645

No data

Variant related genes	Relation type
NRXN1	TF binding region
NRXN1	CpG island
ENSG00000216191	chromatin interactions
ENSG00000179915	chromatin interactions

Extended variants
information (count: 2333 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2333 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12464548	chr2:50855012-50855013	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189273202	chr2:50855022-50855023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553849485	chr2:50855033-50855034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572165317	chr2:50855055-50855056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536288556	chr2:50855059-50855060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554945848	chr2:50855069-50855070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35601736	chr2:50855106-50855107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547419815	chr2:50855132-50855133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181316382	chr2:50855134-50855135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13414145	chr2:50855142-50855143	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs113142345	chr2:50855180-50855181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144218401	chr2:50855198-50855199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541598300	chr2:50855209-50855210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112656371	chr2:50855214-50855215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147759296	chr2:50855247-50855248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541491549	chr2:50855269-50855270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371301740	chr2:50855271-50855272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375924470	chr2:50855302-50855303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530388830	chr2:50855304-50855305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554349903	chr2:50855308-50855309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186367835	chr2:50855374-50855375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570365287	chr2:50855388-50855389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528277548	chr2:50855397-50855398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141239424	chr2:50855440-50855441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72885633	chr2:50855456-50855457	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs113366612	chr2:50855486-50855487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150334760	chr2:50855509-50855510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17539082	chr2:50855558-50855559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570054226	chr2:50855695-50855696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543199204	chr2:50855716-50855717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537000116	chr2:50855718-50855719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559304049	chr2:50855729-50855730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190724274	chr2:50855756-50855757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530925477	chr2:50855773-50855774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371783608	chr2:50855779-50855780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374103091	chr2:50855785-50855786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553585535	chr2:50855830-50855831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144946234	chr2:50855865-50855866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371716873	chr2:50855898-50855899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541921230	chr2:50855903-50855904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563207594	chr2:50855919-50855920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530528005	chr2:50855922-50855923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576307005	chr2:50855951-50855952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79483902	chr2:50855965-50855966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564078290	chr2:50855978-50855979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528365468	chr2:50855985-50855986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375021809	chr2:50855989-50855990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546416887	chr2:50855997-50855998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568229968	chr2:50856041-50856042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1477435	chr2:50856062-50856063	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

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

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50854400-50855200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr2:50854800-50855200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:50854800-50860200	Weak transcription	Fetal Brain Male	brain
4	chr2:50855200-50862600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:50860200-50860400	Enhancers	Fetal Brain Male	brain
6	chr2:50862000-50863600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:50862000-50863800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr2:50862000-50864600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr2:50862600-50863600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:50862600-50864000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr2:50862600-50865800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:50862800-50863800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr2:50862800-50865800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:50863000-50864200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr2:50863000-50864800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr2:50863400-50863800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:50863400-50864000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:50863400-50864000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:50863600-50864000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr2:50863800-50865400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:50864000-50864600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr2:50864000-50865600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr2:50864600-50864800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr2:50864600-50866200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:50865600-50865800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr2:50866200-50866400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr2:50868400-50868600	Enhancers	Fetal Brain Male	brain
28	chr2:50868600-50869000	Enhancers	Fetal Muscle Leg	muscle
29	chr2:50868600-50872200	Weak transcription	Fetal Brain Male	brain
30	chr2:50869000-50875600	Weak transcription	Fetal Muscle Leg	muscle
31	chr2:50872200-50877800	Enhancers	Fetal Brain Male	brain
32	chr2:50872600-50873200	Enhancers	Fetal Brain Female	brain
33	chr2:50872800-50873400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr2:50873000-50873200	Enhancers	Brain Cingulate Gyrus	brain
35	chr2:50873000-50873400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr2:50873000-50873400	Enhancers	Brain Substantia Nigra	brain
37	chr2:50873200-50874000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:50873200-50875600	Weak transcription	Fetal Brain Female	brain
39	chr2:50873200-50875800	Weak transcription	Fetal Kidney	kidney
40	chr2:50873400-50874800	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr2:50873400-50875400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr2:50873400-50875400	Weak transcription	Brain Substantia Nigra	brain
43	chr2:50873600-50873800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr2:50873800-50876800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:50874000-50875600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr2:50874800-50878000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr2:50875200-50876000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr2:50875400-50876000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr2:50875400-50876000	Enhancers	Brain Substantia Nigra	brain
50	chr2:50875400-50877800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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