Variant report

Variant	nsv1004744
Chromosome Location	chr2:51355422-51448953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:184)
Chromatin interactive
region (count:4)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:51439527-51439799	GM12878	blood:	n/a	chr2:51439631-51439642
2	BHLHE40	chr2:51439638-51439779	GM12878	blood:	n/a	n/a
3	CCNT2	chr2:51398751-51398851	K562	blood:	n/a	n/a
4	CEBPB	chr2:51447009-51447209	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:51445233-51445599	IMR90	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
6	CEBPB	chr2:51445259-51445582	HepG2	liver:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
7	CEBPB	chr2:51392842-51393189	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr2:51392868-51393388	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:51445290-51445497	H1-hESC	embryonic stem cell:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
10	CEBPB	chr2:51430897-51430932	A549	lung:	n/a	chr2:51430918-51430929
11	CEBPB	chr2:51376877-51377106	A549	lung:	n/a	n/a
12	CEBPB	chr2:51430857-51430966	H1-hESC	embryonic stem cell:	n/a	chr2:51430918-51430929
13	CEBPB	chr2:51430799-51430988	HepG2	liver:	n/a	chr2:51430918-51430929
14	CEBPB	chr2:51445272-51445575	A549	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
15	CTCF	chr2:51378795-51378863	Fibrobl	skin:	n/a	n/a
16	CTCF	chr2:51373952-51373975	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr2:51405496-51405532	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr2:51431722-51431746	GM20000	blood:	n/a	n/a
19	CTCF	chr2:51365490-51365811	GM12878	blood:	n/a	n/a
20	CTCF	chr2:51399160-51399310	HepG2	liver:	n/a	n/a
21	CTCF	chr2:51389925-51390081	GM12878	blood:	n/a	n/a
22	CTCF	chr2:51404272-51404367	GM12878	blood:	n/a	n/a
23	CTCF	chr2:51365591-51365678	LNCaP	prostate:	n/a	n/a
24	CTCF	chr2:51365651-51365666	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr2:51365672-51365695	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr2:51365600-51365750	HPAF	blood vessel:	n/a	n/a
27	CUX1	chr2:51431162-51431168	GM12878	blood:	n/a	n/a
28	CUX1	chr2:51439433-51439440	GM12878	blood:	n/a	n/a
29	E2F4	chr2:51384024-51384260	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr2:51366837-51366929	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr2:51441537-51441615	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr2:51375315-51375652	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F6	chr2:51446529-51446947	H1-hESC	embryonic stem cell:	n/a	n/a
34	EBF1	chr2:51424390-51424438	GM12878	blood:	n/a	n/a
35	ELK1	chr2:51439695-51439800	GM12878	blood:	n/a	n/a
36	EP300	chr2:51439535-51439862	GM12878	blood:	n/a	n/a
37	EP300	chr2:51368514-51368529	GM12878	blood:	n/a	n/a
38	EP300	chr2:51428389-51428781	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr2:51439610-51439761	GM12878	blood:	n/a	n/a
40	FAM48A	chr2:51442895-51442976	GM12878	blood:	n/a	n/a
41	FAM48A	chr2:51372214-51372379	GM12878	blood:	n/a	n/a
42	FOS	chr2:51385504-51385705	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr2:51445303-51445492	MCF10A-Er-Src	breast:	n/a	chr2:51445336-51445345
44	FOS	chr2:51376982-51377071	MCF10A-Er-Src	breast:	n/a	chr2:51376989-51376996
45	FOS	chr2:51376999-51377053	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr2:51385387-51385714	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr2:51445386-51445425	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr2:51447794-51448467	HUVEC	blood vessel:	n/a	n/a
49	FOS	chr2:51445328-51445440	MCF10A-Er-Src	breast:	n/a	chr2:51445336-51445345
50	FOXA1	chr2:51383022-51383270	T-47D	breast:	n/a	chr2:51383159-51383171

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51378948-51378998	HCM	heart:	n/a
2	chr2:51378948-51378998	HCM	heart:	n/a
3	chr2:51446925-51446975	AG09309	skin:	n/a
4	chr2:51378948-51378998	NHDF-neo	bronchial:	n/a
5	chr2:51378948-51378998	Hela-S3	cervix:	n/a
6	chr2:51446925-51446975	HMEC	breast:	n/a
7	chr2:51446925-51446975	T-47D	breast:	n/a
8	chr2:51379080-51379130	CMK	blood:	n/a
9	chr2:51446925-51446975	Hela-S3	cervix:	n/a
10	chr2:51379080-51379130	SKMC	muscle:	n/a
11	chr2:51378948-51378998	ovcar-3	ovarian:	n/a
12	chr2:51446925-51446975	HNPCEpiC	eye:	n/a
13	chr2:51379080-51379130	ECC-1	luminal epithelium:	n/a
14	chr2:51379080-51379130	GM12878	blood:	n/a
15	chr2:51378948-51378998	CMK	blood:	n/a
16	chr2:51379080-51379130	GM19239	blood:	n/a
17	chr2:51379080-51379130	AG09319	gingival:	n/a
18	chr2:51446925-51446975	AG04449	skin:	fetal
19	chr2:51446925-51446975	HL-60	blood:	n/a
20	chr2:51379080-51379130	NH-A	brain:	n/a
21	chr2:51378948-51378998	PrEC	prostate:	n/a
22	chr2:51378948-51378998	NB4	blood:	n/a
23	chr2:51379080-51379130	HEK293	kidney:	embryo
24	chr2:51446925-51446975	HepG2	liver:	n/a
25	chr2:51378948-51378998	HCF	heart:	n/a
26	chr2:51378948-51378998	BJ	skin:	n/a
27	chr2:51379080-51379130	HRE	kidney:	n/a
28	chr2:51379080-51379130	PANC-1	pancreas:	n/a
29	chr2:51446925-51446975	H1-hESC	embryonic stem cell:	embryo
30	chr2:51379080-51379130	BE2_C	brain:	n/a
31	chr2:51446925-51446975	NH-A	brain:	n/a
32	chr2:51378948-51378998	ProgFib	skin:	n/a
33	chr2:51379080-51379130	GM12892	blood:	n/a
34	chr2:51378948-51378998	BE2_C	brain:	n/a
35	chr2:51378948-51378998	HAEpiC	amniotic membrane:	n/a
36	chr2:51379080-51379130	HCM	heart:	n/a
37	chr2:51446925-51446975	U87	brain:	n/a
38	chr2:51378948-51378998	GM12892	blood:	n/a
39	chr2:51379080-51379130	NT2-D1	testis:	n/a
40	chr2:51446925-51446975	GM06990	blood:	n/a
41	chr2:51446925-51446975	BJ	skin:	n/a
42	chr2:51446925-51446975	SK-N-MC	brain:	n/a
43	chr2:51379080-51379130	RPTEC	kidney:	n/a
44	chr2:51446925-51446975	AoSMC	blood vessel:	n/a
45	chr2:51378948-51378998	GM19239	blood:	n/a
46	chr2:51378948-51378998	AG10803	skin:	n/a
47	chr2:51379080-51379130	HRCEpiC	kidney:	n/a
48	chr2:51446925-51446975	Hepatocyte	liver:	n/a
49	chr2:51379080-51379130	HL-60	blood:	n/a
50	chr2:51378948-51378998	U87	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
2	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
3	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
4	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
2	lnc-NRXN1-4	chr2:51423222-51423493	l_1834_chr2:51413303-51423493_76bGuttman_hLF
3	lnc-NRXN1-1	chr2:51430129-51430286	ENSG00000237374
4	lnc-NRXN1-4	chr2:51414157-51414291	l_1834_chr2:51413303-51423493_76bGuttman_hLF
5	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
6	lnc-NRXN1-4	chr2:51413304-51413539	l_1834_chr2:51413303-51423493_76bGuttman_hLF
7	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
8	lnc-NRXN1-1	chr2:51430129-51430299	ENSG00000237374
9	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374

No data

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

Extended variants
information (count: 1222 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556316535	chr2:51358048-51358049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575886652	chr2:51358070-51358071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374789202	chr2:51358082-51358083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115577283	chr2:51358083-51358084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558419935	chr2:51358101-51358102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184922235	chr2:51358108-51358109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544903716	chr2:51358142-51358143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540927240	chr2:51358160-51358161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188561437	chr2:51358164-51358165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549317391	chr2:51358182-51358183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73930270	chr2:51358295-51358296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181344375	chr2:51358298-51358299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562676116	chr2:51358321-51358322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532951242	chr2:51358325-51358326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544921476	chr2:51358333-51358334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560298073	chr2:51358350-51358351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527551619	chr2:51358353-51358354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111966924	chr2:51358365-51358366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567243252	chr2:51358373-51358374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531363365	chr2:51358437-51358438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115281980	chr2:51358499-51358500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571408822	chr2:51358524-51358525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs199636931	chr2:51358526-51358527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199958687	chr2:51358528-51358529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372895196	chr2:51358531-51358532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs62140670	chr2:51358532-51358533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534783237	chr2:51358533-51358534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141754381	chr2:51358536-51358537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144165981	chr2:51358542-51358543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146329052	chr2:51358547-51358548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148786401	chr2:51358549-51358550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369963342	chr2:51358551-51358552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7566392	chr2:51358553-51358554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10594737	chr2:51358554-51358555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111407208	chr2:51358555-51358556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200217430	chr2:51358557-51358558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200882118	chr2:51358605-51358606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138107674	chr2:51358622-51358623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142812157	chr2:51358629-51358630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146056727	chr2:51358728-51358729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573714643	chr2:51358730-51358731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544160517	chr2:51358781-51358782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115754674	chr2:51358804-51358805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7579236	chr2:51358887-51358888	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs4490226	chr2:51358895-51358896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72878237	chr2:51358907-51358908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560123015	chr2:51358916-51358917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148327578	chr2:51358928-51358929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527460053	chr2:51358950-51358951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542578550	chr2:51358972-51358973	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Bipolar disorder	19114987	CNVD
Bladder cancer	21909424	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51358000-51358400	Enhancers	Fetal Brain Female	brain
2	chr2:51358000-51359000	Enhancers	Fetal Brain Male	brain
3	chr2:51358200-51358800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr2:51372600-51374000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr2:51377000-51379600	Weak transcription	Right Atrium	heart
6	chr2:51377200-51377600	Enhancers	Brain Germinal Matrix	brain
7	chr2:51377600-51382600	Weak transcription	Brain Germinal Matrix	brain
8	chr2:51378800-51379000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:51378800-51379400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:51380000-51381800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:51380200-51380600	Enhancers	Fetal Muscle Leg	muscle
12	chr2:51380400-51380800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:51380400-51381600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr2:51380400-51381600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:51382600-51383400	Enhancers	Brain Germinal Matrix	brain
16	chr2:51392600-51393400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:51392600-51393600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:51392600-51393600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr2:51392800-51393200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:51392800-51393400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr2:51392800-51393400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr2:51392800-51393600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:51392800-51393600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr2:51392800-51393800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:51393000-51393400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:51393000-51393400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr2:51393000-51393400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:51393000-51393400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr2:51393000-51393400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:51393000-51393600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:51393000-51393600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:51393400-51399800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr2:51393600-51396600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:51393600-51397200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr2:51393600-51397400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr2:51396600-51397600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:51397200-51397800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr2:51397400-51397800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr2:51397400-51397800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr2:51397600-51398600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:51398600-51398800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:51435800-51436000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:51436600-51436800	Enhancers	Pancreas	Pancrea
44	chr2:51438800-51439000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr2:51439600-51439800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr2:51440800-51441600	Enhancers	NH-A	brain
47	chr2:51441600-51445600	Weak transcription	NH-A	brain
48	chr2:51443800-51444200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr2:51445600-51447400	Enhancers	NH-A	brain
50	chr2:51446200-51448000	Enhancers	HUES64 Cell Line	embryonic stem cell

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