Variant report

Variant	nsv530833
Chromosome Location	chr2:51292570-51471786
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	chr2:51330523-51330544	HepG2	liver:	n/a	n/a
2	BACH1	chr2:51330505-51330576	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:51439527-51439799	GM12878	blood:	n/a	chr2:51439631-51439642
4	BHLHE40	chr2:51439638-51439779	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:51330297-51330702	HepG2	liver:	n/a	n/a
6	BRCA1	chr2:51330435-51330474	H1-hESC	embryonic stem cell:	n/a	n/a
7	CCNT2	chr2:51398751-51398851	K562	blood:	n/a	n/a
8	CEBPB	chr2:51445290-51445497	H1-hESC	embryonic stem cell:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
9	CEBPB	chr2:51430799-51430988	HepG2	liver:	n/a	chr2:51430918-51430929
10	CEBPB	chr2:51376877-51377106	A549	lung:	n/a	n/a
11	CEBPB	chr2:51461638-51461868	IMR90	lung:	n/a	chr2:51461726-51461737
12	CEBPB	chr2:51335946-51336285	A549	lung:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
13	CEBPB	chr2:51335948-51336305	HepG2	liver:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
14	CEBPB	chr2:51461597-51461861	A549	lung:	n/a	chr2:51461726-51461737
15	CEBPB	chr2:51392868-51393388	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:51325442-51325765	IMR90	lung:	n/a	chr2:51325594-51325607
17	CEBPB	chr2:51335993-51336283	H1-hESC	embryonic stem cell:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
18	CEBPB	chr2:51328029-51328351	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:51445259-51445582	HepG2	liver:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
20	CEBPB	chr2:51314497-51314768	A549	lung:	n/a	chr2:51314679-51314692 chr2:51314681-51314692 chr2:51314679-51314692 chr2:51314681-51314692
21	CEBPB	chr2:51445233-51445599	IMR90	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
22	CEBPB	chr2:51335946-51336321	K562	blood:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
23	CEBPB	chr2:51324687-51324910	HepG2	liver:	n/a	chr2:51324819-51324830
24	CEBPB	chr2:51325500-51325735	H1-hESC	embryonic stem cell:	n/a	chr2:51325594-51325607
25	CEBPB	chr2:51392842-51393189	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr2:51461631-51461892	HepG2	liver:	n/a	chr2:51461726-51461737
27	CEBPB	chr2:51330315-51330732	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:51335948-51336306	IMR90	lung:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
29	CEBPB	chr2:51335991-51336268	Hela-S3	cervix:	n/a	chr2:51336127-51336140 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336129-51336138 chr2:51336127-51336138 chr2:51336129-51336138 chr2:51336127-51336140 chr2:51336128-51336139
30	CEBPB	chr2:51330496-51330704	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:51447009-51447209	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:51445272-51445575	A549	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
33	CEBPB	chr2:51430857-51430966	H1-hESC	embryonic stem cell:	n/a	chr2:51430918-51430929
34	CEBPB	chr2:51430897-51430932	A549	lung:	n/a	chr2:51430918-51430929
35	CHD2	chr2:51301746-51301806	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr2:51330420-51330623	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:51330400-51330550	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr2:51328080-51328230	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr2:51373952-51373975	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr2:51307306-51307343	Lung_OC	lung:	n/a	n/a
41	CTCF	chr2:51330378-51330621	Gliobla	brain:	n/a	n/a
42	CTCF	chr2:51365490-51365811	GM12878	blood:	n/a	n/a
43	CTCF	chr2:51300710-51300762	GM10266	blood:	n/a	n/a
44	CTCF	chr2:51468664-51468715	Lung_OC	lung:	n/a	n/a
45	CTCF	chr2:51365600-51365750	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr2:51405496-51405532	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr2:51312020-51312170	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr2:51330470-51330523	ProgFib	skin:	n/a	n/a
49	CTCF	chr2:51312000-51312150	NHEK	skin:	n/a	n/a
50	CTCF	chr2:51311960-51312110	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51379080-51379130	IMR90	lung:	fetal
2	chr2:51379080-51379130	IMR90	lung:	fetal
3	chr2:51446925-51446975	HCPEpiC	choroid plexus:	n/a
4	chr2:51378948-51378998	H1-hESC	embryonic stem cell:	embryo
5	chr2:51379080-51379130	HCF	heart:	n/a
6	chr2:51446925-51446975	GM12892	blood:	n/a
7	chr2:51378948-51378998	NHDF-neo	bronchial:	n/a
8	chr2:51446925-51446975	AG10803	skin:	n/a
9	chr2:51378948-51378998	ovcar-3	ovarian:	n/a
10	chr2:51446925-51446975	HRE	kidney:	n/a
11	chr2:51379080-51379130	NT2-D1	testis:	n/a
12	chr2:51379080-51379130	SK-N-SH	brain:	n/a
13	chr2:51379080-51379130	AG09319	gingival:	n/a
14	chr2:51378948-51378998	HCM	heart:	n/a
15	chr2:51379080-51379130	AoSMC	blood vessel:	n/a
16	chr2:51379080-51379130	RPTEC	kidney:	n/a
17	chr2:51379080-51379130	ProgFib	skin:	n/a
18	chr2:51379080-51379130	HepG2	liver:	n/a
19	chr2:51379080-51379130	A549	lung:	n/a
20	chr2:51378948-51378998	MCF-7	breast:	n/a
21	chr2:51446925-51446975	HAEpiC	amniotic membrane:	n/a
22	chr2:51446925-51446975	ECC-1	luminal epithelium:	n/a
23	chr2:51446925-51446975	PANC-1	pancreas:	n/a
24	chr2:51378948-51378998	HMEC	breast:	n/a
25	chr2:51379080-51379130	HL-60	blood:	n/a
26	chr2:51379080-51379130	HUVEC	blood vessel:	n/a
27	chr2:51446925-51446975	MCF-7	breast:	n/a
28	chr2:51378948-51378998	IMR90	lung:	fetal
29	chr2:51446925-51446975	AG09309	skin:	n/a
30	chr2:51378948-51378998	HCF	heart:	n/a
31	chr2:51379080-51379130	AG09309	skin:	n/a
32	chr2:51446925-51446975	T-47D	breast:	n/a
33	chr2:51446925-51446975	Caco-2	colon:	n/a
34	chr2:51378948-51378998	K562	blood:	n/a
35	chr2:51379080-51379130	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:51379080-51379130	T-47D	breast:	n/a
37	chr2:51378948-51378998	HRPEpiC	eye:	n/a
38	chr2:51446925-51446975	HCF	heart:	n/a
39	chr2:51379080-51379130	SAEC	small airway:	n/a
40	chr2:51379080-51379130	Hela-S3	cervix:	n/a
41	chr2:51379080-51379130	MCF10A-Er-Src	breast:	n/a
42	chr2:51446925-51446975	NHBE	bronchial:	n/a
43	chr2:51378948-51378998	RPTEC	kidney:	n/a
44	chr2:51379080-51379130	MCF-7	breast:	n/a
45	chr2:51379080-51379130	HMEC	breast:	n/a
46	chr2:51446925-51446975	NT2-D1	testis:	n/a
47	chr2:51446925-51446975	BJ	skin:	n/a
48	chr2:51378948-51378998	NHBE	bronchial:	n/a
49	chr2:51379080-51379130	SK-N-MC	brain:	n/a
50	chr2:51378948-51378998	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
2	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
3	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
4	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
5	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
6	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
7	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
8	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-4	chr2:51423222-51423493	l_1834_chr2:51413303-51423493_76bGuttman_hLF
2	lnc-NRXN1-1	chr2:51430129-51430299	ENSG00000237374
3	lnc-NRXN1-4	chr2:51414157-51414291	l_1834_chr2:51413303-51423493_76bGuttman_hLF
4	lnc-NRXN1-3	chr2:51294575-51294743	l_1833_chr2:51283578-51306188_testes
5	lnc-NRXN1-3	chr2:51302313-51302437	l_1833_chr2:51283578-51306188_testes
6	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
7	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
8	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
9	lnc-NRXN1-1	chr2:51430129-51430286	ENSG00000237374
10	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
11	lnc-NRXN1-3	chr2:51306149-51306209	l_1833_chr2:51283578-51306188_testes
12	lnc-NRXN1-3	chr2:51302314-51302406	NONHSAT070652
13	lnc-NRXN1-4	chr2:51413304-51413539	l_1834_chr2:51413303-51423493_76bGuttman_hLF

Variant related genes	Relation type
ENSG00000237374	TF binding region
ENSG00000237374	CpG island

Extended variants
information (count: 3370 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3370 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74703280	chr2:51292623-51292624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78345923	chr2:51292624-51292625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74733780	chr2:51292625-51292626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568657583	chr2:51292628-51292629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183497625	chr2:51292636-51292637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557268856	chr2:51292651-51292652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543850343	chr2:51292695-51292696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188488977	chr2:51292702-51292703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575214934	chr2:51292710-51292711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539497769	chr2:51292713-51292714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558225053	chr2:51292719-51292720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191967059	chr2:51292767-51292768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565197362	chr2:51292775-51292776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540724986	chr2:51292798-51292799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34725304	chr2:51292831-51292832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561704867	chr2:51292866-51292867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77194941	chr2:51292875-51292876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142437356	chr2:51292892-51292893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7603441	chr2:51292893-51292894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562817483	chr2:51292917-51292918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535173502	chr2:51292934-51292935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183350539	chr2:51292938-51292939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544980194	chr2:51292951-51292952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73930254	chr2:51292992-51292993	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs186942405	chr2:51292994-51292995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147030099	chr2:51294607-51294608	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs181089779	chr2:51294636-51294637	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs74856626	chr2:51294663-51294664	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs13021621	chr2:51294688-51294689	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571443068	chr2:51294696-51294697	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs375100037	chr2:51294730-51294731	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs13022010	chr2:51294736-51294737	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564668050	chr2:51295001-51295002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138436090	chr2:51295040-51295041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115923823	chr2:51295055-51295056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370406208	chr2:51295056-51295057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560522793	chr2:51295070-51295071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527957395	chr2:51295096-51295097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143910055	chr2:51295097-51295098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561248831	chr2:51295121-51295122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183526422	chr2:51295215-51295216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186376207	chr2:51295235-51295236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190932899	chr2:51295241-51295242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147302119	chr2:51295249-51295250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138864237	chr2:51295254-51295255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565761238	chr2:51295275-51295276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536514131	chr2:51295290-51295291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554478552	chr2:51295313-51295314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182358341	chr2:51295355-51295356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117316953	chr2:51295360-51295361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Schizophrenia	17989066	CNVD
Bipolar disorder	19114987	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51291800-51292800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr2:51292400-51292800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:51292400-51293000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:51295000-51303600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:51295400-51295600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:51295400-51295800	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr2:51295400-51299400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:51295600-51296600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:51295800-51297000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr2:51296600-51298200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:51297000-51297200	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr2:51297000-51298400	Enhancers	Primary hematopoietic stem cells	blood
13	chr2:51297200-51298800	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr2:51297600-51298400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr2:51298000-51298800	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr2:51298200-51298600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr2:51298600-51299400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:51299800-51300000	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr2:51299800-51300400	Enhancers	Liver	Liver
20	chr2:51300200-51300400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:51300400-51301800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:51301600-51301800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr2:51301600-51304000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr2:51301800-51302600	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr2:51301800-51304400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:51302400-51303400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr2:51302600-51303000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr2:51302600-51303000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr2:51302600-51303400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr2:51302600-51303400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:51303000-51303200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr2:51303200-51303600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr2:51303600-51304400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr2:51304400-51304600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:51311000-51311600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:51311600-51313400	Enhancers	Placenta Amnion	Placenta Amnion
37	chr2:51312800-51313000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr2:51313600-51318200	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr2:51318200-51318600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr2:51320200-51320800	Active TSS	Stomach Smooth Muscle	stomach
41	chr2:51320600-51321000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:51320800-51321000	Enhancers	Psoas Muscle	Psoas
43	chr2:51321000-51321200	Weak transcription	Psoas Muscle	Psoas
44	chr2:51321000-51325800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:51323000-51323600	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr2:51325800-51326400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:51326400-51330000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:51328200-51328400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr2:51328200-51328400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr2:51328200-51328600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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