Variant report

Variant	nsv581870
Chromosome Location	chr2:51308075-51479170
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	chr2:51461597-51461861	A549	lung:	n/a	chr2:51461726-51461737
9	CEBPB	chr2:51330496-51330704	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:51330315-51330732	IMR90	lung:	n/a	n/a
11	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
12	CEBPB	chr2:51445290-51445497	H1-hESC	embryonic stem cell:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
13	CEBPB	chr2:51447009-51447209	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:51445259-51445582	HepG2	liver:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
15	CEBPB	chr2:51461638-51461868	IMR90	lung:	n/a	chr2:51461726-51461737
16	CEBPB	chr2:51324687-51324910	HepG2	liver:	n/a	chr2:51324819-51324830
17	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
18	CEBPB	chr2:51314497-51314768	A549	lung:	n/a	chr2:51314679-51314692 chr2:51314681-51314692 chr2:51314679-51314692 chr2:51314681-51314692
19	CEBPB	chr2:51445272-51445575	A549	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
20	CEBPB	chr2:51376877-51377106	A549	lung:	n/a	n/a
21	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
22	CEBPB	chr2:51392842-51393189	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:51445233-51445599	IMR90	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
24	CEBPB	chr2:51325442-51325765	IMR90	lung:	n/a	chr2:51325594-51325607
25	CEBPB	chr2:51461631-51461892	HepG2	liver:	n/a	chr2:51461726-51461737
26	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
27	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
28	CEBPB	chr2:51392868-51393388	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:51325500-51325735	H1-hESC	embryonic stem cell:	n/a	chr2:51325594-51325607
30	CEBPB	chr2:51430897-51430932	A549	lung:	n/a	chr2:51430918-51430929
31	CEBPB	chr2:51430857-51430966	H1-hESC	embryonic stem cell:	n/a	chr2:51430918-51430929
32	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
33	CEBPB	chr2:51328029-51328351	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr2:51430799-51430988	HepG2	liver:	n/a	chr2:51430918-51430929
35	CHD2	chr2:51330420-51330623	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr2:51330470-51330523	ProgFib	skin:	n/a	n/a
37	CTCF	chr2:51330419-51330508	HepG2	liver:	n/a	n/a
38	CTCF	chr2:51330447-51330575	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr2:51474460-51474610	NB4	blood:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
40	CTCF	chr2:51474571-51474598	LNCaP	prostate:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
41	CTCF	chr2:51474480-51474630	BE2_C	brain:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
42	CTCF	chr2:51365600-51365750	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr2:51455939-51455997	GM20000	blood:	n/a	n/a
44	CTCF	chr2:51365651-51365666	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr2:51330374-51330638	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr2:51474561-51474645	H1-hESC	embryonic stem cell:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
47	CTCF	chr2:51468664-51468715	Lung_OC	lung:	n/a	n/a
48	CTCF	chr2:51330464-51330538	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:51474540-51474690	WERI-Rb-1	eye:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
50	CTCF	chr2:51474620-51474770	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51378948-51378998	SAEC	small airway:	n/a
2	chr2:51378948-51378998	HRE	kidney:	n/a
3	chr2:51446925-51446975	BE2_C	brain:	n/a
4	chr2:51378948-51378998	HMEC	breast:	n/a
5	chr2:51446925-51446975	LNCaP	prostate:	n/a
6	chr2:51446925-51446975	AG04450	lung:	fetal
7	chr2:51379080-51379130	HL-60	blood:	n/a
8	chr2:51379080-51379130	HRCEpiC	kidney:	n/a
9	chr2:51378948-51378998	SK-N-MC	brain:	n/a
10	chr2:51379080-51379130	NHBE	bronchial:	n/a
11	chr2:51446925-51446975	HCT-116	colon:	n/a
12	chr2:51378948-51378998	ProgFib	skin:	n/a
13	chr2:51378948-51378998	GM12891	blood:	n/a
14	chr2:51446925-51446975	PANC-1	pancreas:	n/a
15	chr2:51379080-51379130	MCF10A-Er-Src	breast:	n/a
16	chr2:51446925-51446975	SAEC	small airway:	n/a
17	chr2:51446925-51446975	HRE	kidney:	n/a
18	chr2:51446925-51446975	GM12891	blood:	n/a
19	chr2:51379080-51379130	H1-hESC	embryonic stem cell:	embryo
20	chr2:51446925-51446975	Caco-2	colon:	n/a
21	chr2:51379080-51379130	HEK293	kidney:	embryo
22	chr2:51446925-51446975	PFSK-1	brain:	n/a
23	chr2:51446925-51446975	PrEC	prostate:	n/a
24	chr2:51446925-51446975	Hepatocyte	liver:	n/a
25	chr2:51378948-51378998	GM06990	blood:	n/a
26	chr2:51378948-51378998	AG10803	skin:	n/a
27	chr2:51379080-51379130	ProgFib	skin:	n/a
28	chr2:51379080-51379130	HRE	kidney:	n/a
29	chr2:51379080-51379130	GM06990	blood:	n/a
30	chr2:51378948-51378998	PFSK-1	brain:	n/a
31	chr2:51446925-51446975	K562	blood:	n/a
32	chr2:51378948-51378998	NH-A	brain:	n/a
33	chr2:51378948-51378998	LNCaP	prostate:	n/a
34	chr2:51378948-51378998	AoSMC	blood vessel:	n/a
35	chr2:51379080-51379130	A549	lung:	n/a
36	chr2:51379080-51379130	SKMC	muscle:	n/a
37	chr2:51378948-51378998	Hela-S3	cervix:	n/a
38	chr2:51379080-51379130	HepG2	liver:	n/a
39	chr2:51379080-51379130	IMR90	lung:	fetal
40	chr2:51378948-51378998	HepG2	liver:	n/a
41	chr2:51378948-51378998	SKMC	muscle:	n/a
42	chr2:51446925-51446975	SK-N-SH_RA	brain:	n/a
43	chr2:51378948-51378998	H1-hESC	embryonic stem cell:	embryo
44	chr2:51446925-51446975	GM19239	blood:	n/a
45	chr2:51379080-51379130	LNCaP	prostate:	n/a
46	chr2:51446925-51446975	HRPEpiC	eye:	n/a
47	chr2:51378948-51378998	HCPEpiC	choroid plexus:	n/a
48	chr2:51379080-51379130	HIPEpiC	eye:	n/a
49	chr2:51379080-51379130	GM12892	blood:	n/a
50	chr2:51379080-51379130	K562	blood:	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	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
4	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
5	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
6	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
7	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
8	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-1	chr2:51430129-51430299	ENSG00000237374
2	lnc-NRXN1-4	chr2:51414157-51414291	l_1834_chr2:51413303-51423493_76bGuttman_hLF
3	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
4	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
5	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
6	lnc-NRXN1-4	chr2:51423222-51423493	l_1834_chr2:51413303-51423493_76bGuttman_hLF
7	lnc-NRXN1-1	chr2:51430129-51430286	ENSG00000237374
8	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
9	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: 2992 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2992 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545390219	chr2:51311020-51311021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554149904	chr2:51311057-51311058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544581325	chr2:51311109-51311110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572430839	chr2:51311174-51311175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543134547	chr2:51311199-51311200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560921629	chr2:51311217-51311218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531442423	chr2:51311218-51311219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182918459	chr2:51311220-51311221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117937870	chr2:51311249-51311250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532290015	chr2:51311314-51311315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564590824	chr2:51311341-51311342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565697195	chr2:51311354-51311355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187217093	chr2:51311388-51311389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548304483	chr2:51311414-51311415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192693813	chr2:51311506-51311507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538391786	chr2:51311522-51311523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs17575302	chr2:51311532-51311533	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs571944808	chr2:51311534-51311535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185520182	chr2:51311578-51311579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553867068	chr2:51311637-51311638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73930260	chr2:51311649-51311650	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs148498898	chr2:51311672-51311673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555001286	chr2:51311690-51311691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142780521	chr2:51311692-51311693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574297486	chr2:51311706-51311707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536922545	chr2:51311874-51311875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540352510	chr2:51311879-51311880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370419538	chr2:51311880-51311881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188015861	chr2:51311896-51311897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192243831	chr2:51311909-51311910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376957247	chr2:51311962-51311963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146584787	chr2:51311975-51311976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529738493	chr2:51311987-51311988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367928237	chr2:51312011-51312012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs956189	chr2:51312012-51312013	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs569724894	chr2:51312049-51312050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530647408	chr2:51312070-51312071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550378907	chr2:51312101-51312102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372562138	chr2:51312109-51312110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs6750228	chr2:51312124-51312125	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs548117276	chr2:51312140-51312141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184353315	chr2:51312175-51312176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536608234	chr2:51312214-51312215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554681735	chr2:51312262-51312263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs369694321	chr2:51312278-51312279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529464398	chr2:51312283-51312284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373444915	chr2:51312288-51312289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577154391	chr2:51312298-51312299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188745724	chr2:51312312-51312313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112643687	chr2:51312314-51312315	Enhancers	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:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51311000-51311600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:51311600-51313400	Enhancers	Placenta Amnion	Placenta Amnion
3	chr2:51312800-51313000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr2:51313600-51318200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:51318200-51318600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr2:51320200-51320800	Active TSS	Stomach Smooth Muscle	stomach
7	chr2:51320600-51321000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:51320800-51321000	Enhancers	Psoas Muscle	Psoas
9	chr2:51321000-51321200	Weak transcription	Psoas Muscle	Psoas
10	chr2:51321000-51325800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr2:51323000-51323600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr2:51325800-51326400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:51326400-51330000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:51328200-51328400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr2:51328200-51328400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:51328200-51328600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr2:51328600-51329800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr2:51328600-51330200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr2:51329000-51330400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:51329400-51330400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr2:51329600-51331000	Enhancers	Primary hematopoietic stem cells	blood
22	chr2:51329800-51330200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:51329800-51330400	Enhancers	H9 Cell Line	embryonic stem cell
24	chr2:51329800-51330400	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr2:51329800-51330600	Enhancers	Brain Cingulate Gyrus	brain
26	chr2:51329800-51330800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr2:51329800-51331000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr2:51329800-51331000	Enhancers	Placenta Amnion	Placenta Amnion
29	chr2:51330000-51330200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:51330000-51330400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr2:51330000-51330600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr2:51330000-51330800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr2:51330000-51331000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr2:51330000-51331000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr2:51330000-51331000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr2:51330000-51331000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:51330000-51331000	Enhancers	Fetal Muscle Trunk	muscle
38	chr2:51330000-51331000	Enhancers	Placenta	Placenta
39	chr2:51330200-51330400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr2:51330200-51330600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr2:51330200-51330600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr2:51330200-51330600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr2:51330200-51330600	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr2:51330200-51330800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:51330200-51330800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr2:51330200-51331000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:51330200-51331000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:51330200-51331000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr2:51330200-51331000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr2:51330200-51331000	Enhancers	Fetal Heart	heart

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