Variant report

Variant	nsv2724
Chromosome Location	chr2:50688876-50734321
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	chr2:50718755-50718994	HepG2	liver:	n/a	n/a
2	BHLHE40	chr2:50718813-50718826	K562	blood:	n/a	n/a
3	BHLHE40	chr2:50719650-50719971	GM12878	blood:	n/a	n/a
4	BRCA1	chr2:50719632-50719941	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr2:50693361-50693581	HepG2	liver:	n/a	chr2:50693455-50693466
6	CTCF	chr2:50719700-50719850	HPAF	blood vessel:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
7	CTCF	chr2:50718760-50718910	AG09319	gingival:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
8	CTCF	chr2:50719623-50719935	HUVEC	blood vessel:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
9	CTCF	chr2:50719720-50719870	GM12873	blood:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
10	CTCF	chr2:50703466-50703555	GM13977	blood:	n/a	n/a
11	CTCF	chr2:50719180-50719330	GM12867	blood:	n/a	n/a
12	CTCF	chr2:50718778-50718938	SK-N-SH_RA	brain:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
13	CTCF	chr2:50718820-50718970	AoAF	blood vessel:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
14	CTCF	chr2:50719691-50719927	GM13977	blood:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
15	CTCF	chr2:50718724-50719021	GM12878	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
16	CTCF	chr2:50718640-50719093	MCF-7	breast:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
17	CTCF	chr2:50719668-50719886	A549	lung:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
18	CTCF	chr2:50717400-50717550	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr2:50719700-50719850	AG09319	gingival:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
20	CTCF	chr2:50719720-50719870	AG04450	lung:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
21	CTCF	chr2:50718800-50718950	SAEC	small airway:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
22	CTCF	chr2:50719380-50719530	NHEK	skin:	n/a	n/a
23	CTCF	chr2:50703500-50703650	RPTEC	kidney:	n/a	n/a
24	CTCF	chr2:50703420-50703570	HepG2	liver:	n/a	n/a
25	CTCF	chr2:50719740-50719890	GM06990	blood:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
26	CTCF	chr2:50703420-50703570	HAc	cerebellar:	n/a	n/a
27	CTCF	chr2:50718800-50718950	BJ	skin:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
28	CTCF	chr2:50719579-50720023	K562	blood:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
29	CTCF	chr2:50703420-50703570	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr2:50719780-50719930	GM12875	blood:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
31	CTCF	chr2:50719700-50719850	GM12865	blood:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
32	CTCF	chr2:50718880-50719030	HVMF	connective:	n/a	n/a
33	CTCF	chr2:50703420-50703570	HCT-116	colon:	n/a	n/a
34	CTCF	chr2:50719660-50719810	AG04450	lung:	n/a	chr2:50719800-50719808
35	CTCF	chr2:50703344-50703697	GM12878	blood:	n/a	n/a
36	CTCF	chr2:50719740-50719890	GM12864	blood:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
37	CTCF	chr2:50719780-50719930	WI-38	lung:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
38	CTCF	chr2:50718740-50718890	GM12868	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
39	CTCF	chr2:50718780-50718930	GM12801	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
40	CTCF	chr2:50718820-50718970	GM12871	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
41	CTCF	chr2:50718800-50718950	GM12873	blood:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
42	CTCF	chr2:50720140-50720290	NHLF	lung:	n/a	n/a
43	CTCF	chr2:50703420-50703570	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr2:50719720-50719870	AG10803	skin:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
45	CTCF	chr2:50719680-50719830	GM12878	blood:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
46	CTCF	chr2:50719700-50719850	HepG2	liver:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
47	CTCF	chr2:50703509-50703543	K562	blood:	n/a	n/a
48	CTCF	chr2:50719720-50719870	NHDF-neo	bronchial:	n/a	chr2:50719790-50719811 chr2:50719800-50719808 chr2:50719796-50719812 chr2:50719795-50719813
49	CTCF	chr2:50718747-50718983	Pancreas_OC	pancreas:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882
50	CTCF	chr2:50718740-50718890	HEK293	kidney:	n/a	chr2:50718868-50718889 chr2:50718866-50718884 chr2:50718869-50718882

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50718584-50718634	MCF10A-Er-Src	breast:	n/a
2	chr2:50718584-50718634	SKMC	muscle:	n/a
3	chr2:50718584-50718634	ovcar-3	ovarian:	n/a
4	chr2:50718584-50718634	SAEC	small airway:	n/a
5	chr2:50718584-50718634	GM12891	blood:	n/a
6	chr2:50718584-50718634	HNPCEpiC	eye:	n/a
7	chr2:50718584-50718634	NHBE	bronchial:	n/a
8	chr2:50718584-50718634	HEK293	kidney:	embryo
9	chr2:50718584-50718634	HepG2	liver:	n/a
10	chr2:50718584-50718634	H1-hESC	embryonic stem cell:	embryo
11	chr2:50718584-50718634	A549	lung:	n/a
12	chr2:50718584-50718634	PANC-1	pancreas:	n/a
13	chr2:50718584-50718634	HMEC	breast:	n/a
14	chr2:50718584-50718634	ProgFib	skin:	n/a
15	chr2:50718584-50718634	HUVEC	blood vessel:	n/a
16	chr2:50718584-50718634	NH-A	brain:	n/a
17	chr2:50718584-50718634	Hepatocyte	liver:	n/a
18	chr2:50718584-50718634	HAEpiC	amniotic membrane:	n/a
19	chr2:50718584-50718634	LNCaP	prostate:	n/a
20	chr2:50718584-50718634	HL-60	blood:	n/a
21	chr2:50718584-50718634	GM12878	blood:	n/a
22	chr2:50718584-50718634	Caco-2	colon:	n/a
23	chr2:50718584-50718634	SK-N-SH_RA	brain:	n/a
24	chr2:50718584-50718634	CMK	blood:	n/a
25	chr2:50718584-50718634	T-47D	breast:	n/a
26	chr2:50718584-50718634	PrEC	prostate:	n/a
27	chr2:50718584-50718634	GM12892	blood:	n/a
28	chr2:50718584-50718634	HCPEpiC	choroid plexus:	n/a
29	chr2:50718584-50718634	AG09309	skin:	n/a
30	chr2:50718584-50718634	AG09319	gingival:	n/a
31	chr2:50718584-50718634	HRCEpiC	kidney:	n/a
32	chr2:50718584-50718634	U87	brain:	n/a
33	chr2:50718584-50718634	GM06990	blood:	n/a
34	chr2:50718584-50718634	AG04449	skin:	fetal
35	chr2:50718584-50718634	HRPEpiC	eye:	n/a
36	chr2:50718584-50718634	BE2_C	brain:	n/a
37	chr2:50718584-50718634	PFSK-1	brain:	n/a
38	chr2:50718584-50718634	RPTEC	kidney:	n/a
39	chr2:50718584-50718634	HCT-116	colon:	n/a
40	chr2:50718584-50718634	GM19239	blood:	n/a
41	chr2:50718584-50718634	BJ	skin:	n/a
42	chr2:50718584-50718634	AG10803	skin:	n/a
43	chr2:50718584-50718634	ECC-1	luminal epithelium:	n/a
44	chr2:50718584-50718634	NT2-D1	testis:	n/a
45	chr2:50718584-50718634	HRE	kidney:	n/a
46	chr2:50718584-50718634	Jurkat	blood:	n/a
47	chr2:50718584-50718634	HPAEpiC	pulmonary alveolar:	n/a
48	chr2:50718584-50718634	AoSMC	blood vessel:	n/a
49	chr2:50718584-50718634	NB4	blood:	n/a
50	chr2:50718584-50718634	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:50712217..50714362-chr2:50715383..50718092,2	MCF-7	breast:
2	chr2:50698680..50701343-chr2:50702519..50705361,2	K562	blood:
3	chr2:50551521..50552446-chr2:50719322..50720205,2	MCF-7	breast:
4	chr2:50712217..50714362-chr2:50715383..50718092,2	MCF-7	breast:
5	chr2:50629632..50630141-chr2:50719329..50719849,2	MCF-7	breast:
6	chr2:50699843..50701598-chr2:50702519..50705507,3	K562	blood:
7	chr2:50698680..50701343-chr2:50702519..50705361,2	K562	blood:
8	chr2:50571653..50572272-chr2:50719383..50719965,2	MCF-7	breast:
9	chr2:48772065..48772805-chr2:50719351..50720113,2	K562	blood:
10	chr2:50699843..50701598-chr2:50702519..50705507,3	K562	blood:

Variant related genes	Relation type
NRXN1	TF binding region
NRXN1	CpG island

Extended variants
information (count: 2340 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2340 , 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	rs575316713	chr2:50688877-50688878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543900804	chr2:50688938-50688939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565192490	chr2:50688968-50688969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532640996	chr2:50688970-50688971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138978154	chr2:50688989-50688990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182936167	chr2:50689032-50689033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530448337	chr2:50689054-50689055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564411012	chr2:50689079-50689080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548563242	chr2:50689080-50689081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570106139	chr2:50689101-50689102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532535077	chr2:50689112-50689113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570254674	chr2:50689122-50689123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113468559	chr2:50689139-50689140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187715219	chr2:50689172-50689173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570255402	chr2:50689208-50689209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141427956	chr2:50689210-50689211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552578992	chr2:50689212-50689213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567703049	chr2:50689219-50689220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369346688	chr2:50689232-50689233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552733787	chr2:50689240-50689241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535757128	chr2:50689254-50689255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12997031	chr2:50689260-50689261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575405784	chr2:50689263-50689264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534920747	chr2:50689268-50689269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555103500	chr2:50689270-50689271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147045187	chr2:50689328-50689329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568662371	chr2:50689345-50689346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114615812	chr2:50689364-50689365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577440206	chr2:50689389-50689390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376340886	chr2:50689395-50689396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370422758	chr2:50689455-50689456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190949254	chr2:50689467-50689468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115372881	chr2:50689469-50689470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530085033	chr2:50689473-50689474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542515033	chr2:50689479-50689480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138271829	chr2:50689484-50689485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34976254	chr2:50689526-50689527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369250333	chr2:50689528-50689529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552543809	chr2:50689553-50689554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113172583	chr2:50689565-50689566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528207546	chr2:50689579-50689580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537794940	chr2:50689586-50689587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557358455	chr2:50689594-50689595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141903441	chr2:50689693-50689694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182843290	chr2:50689726-50689727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112056883	chr2:50689741-50689742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187129175	chr2:50689742-50689743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192201184	chr2:50689743-50689744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75098492	chr2:50689780-50689781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184365988	chr2:50689785-50689786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50684000-50691800	Weak transcription	Brain Germinal Matrix	brain
2	chr2:50691000-50691200	Enhancers	Fetal Brain Female	brain
3	chr2:50691200-50711600	Weak transcription	Fetal Brain Female	brain
4	chr2:50691200-50716000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:50691400-50703000	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:50691600-50718600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:50691800-50692000	Enhancers	Brain Germinal Matrix	brain
8	chr2:50692000-50692400	Weak transcription	Brain Germinal Matrix	brain
9	chr2:50692400-50692600	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr2:50692400-50695600	Enhancers	Brain Germinal Matrix	brain
11	chr2:50692600-50705400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr2:50695200-50696200	Enhancers	Stomach Mucosa	stomach
13	chr2:50695600-50709400	Weak transcription	Brain Germinal Matrix	brain
14	chr2:50696600-50698000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:50697000-50697400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr2:50697000-50697400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:50699000-50742000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr2:50702600-50702800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr2:50703000-50703200	Enhancers	Brain Hippocampus Middle	brain
20	chr2:50704400-50705000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr2:50704400-50718600	Weak transcription	Fetal Brain Male	brain
22	chr2:50704800-50705200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:50705200-50706200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:50705400-50706200	Enhancers	Stomach Mucosa	stomach
25	chr2:50705400-50706600	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr2:50706200-50719000	Weak transcription	Stomach Mucosa	stomach
27	chr2:50706400-50706600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:50706600-50719400	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr2:50709400-50710000	Strong transcription	Brain Germinal Matrix	brain
30	chr2:50710000-50712400	Weak transcription	Brain Germinal Matrix	brain
31	chr2:50711600-50716600	Strong transcription	Fetal Brain Female	brain
32	chr2:50712400-50714600	Strong transcription	Brain Germinal Matrix	brain
33	chr2:50712600-50718800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr2:50713400-50718200	Weak transcription	Brain Angular Gyrus	brain
35	chr2:50714600-50715800	Weak transcription	Brain Germinal Matrix	brain
36	chr2:50714600-50718600	Weak transcription	Brain Anterior Caudate	brain
37	chr2:50715800-50716200	Strong transcription	Brain Germinal Matrix	brain
38	chr2:50716000-50716200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr2:50716000-50716200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr2:50716000-50716400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr2:50716000-50717800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr2:50716200-50717000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:50716200-50718600	Weak transcription	Brain Germinal Matrix	brain
44	chr2:50716400-50717400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr2:50716400-50719200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr2:50716600-50719000	Weak transcription	Fetal Brain Female	brain
47	chr2:50717000-50717400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:50717200-50717400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:50717400-50717600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:50717400-50718400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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