Variant report

Variant	nsv457674
Chromosome Location	chr2:51368539-51476956
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	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	chr2:51445272-51445575	A549	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
5	CEBPB	chr2:51376877-51377106	A549	lung:	n/a	n/a
6	CEBPB	chr2:51461631-51461892	HepG2	liver:	n/a	chr2:51461726-51461737
7	CEBPB	chr2:51392842-51393189	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr2:51447009-51447209	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr2:51430799-51430988	HepG2	liver:	n/a	chr2:51430918-51430929
10	CEBPB	chr2:51392868-51393388	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:51445233-51445599	IMR90	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
12	CEBPB	chr2:51461638-51461868	IMR90	lung:	n/a	chr2:51461726-51461737
13	CEBPB	chr2:51430897-51430932	A549	lung:	n/a	chr2:51430918-51430929
14	CEBPB	chr2:51461597-51461861	A549	lung:	n/a	chr2:51461726-51461737
15	CEBPB	chr2:51445290-51445497	H1-hESC	embryonic stem cell:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
16	CEBPB	chr2:51445259-51445582	HepG2	liver:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
17	CEBPB	chr2:51430857-51430966	H1-hESC	embryonic stem cell:	n/a	chr2:51430918-51430929
18	CTCF	chr2:51474480-51474630	Caco-2	colon:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
19	CTCF	chr2:51404272-51404367	GM12878	blood:	n/a	n/a
20	CTCF	chr2:51474545-51474665	HepG2	liver:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
21	CTCF	chr2:51378795-51378863	Fibrobl	skin:	n/a	n/a
22	CTCF	chr2:51474540-51474690	WERI-Rb-1	eye:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
23	CTCF	chr2:51405496-51405532	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr2:51474480-51474630	BE2_C	brain:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
25	CTCF	chr2:51474391-51474673	H1-hESC	embryonic stem cell:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
26	CTCF	chr2:51474556-51474571	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr2:51474584-51474618	A549	lung:	n/a	n/a
28	CTCF	chr2:51474520-51474670	BE2_C	brain:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
29	CTCF	chr2:51474620-51474770	A549	lung:	n/a	n/a
30	CTCF	chr2:51468664-51468715	Lung_OC	lung:	n/a	n/a
31	CTCF	chr2:51474504-51474628	HepG2	liver:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
32	CTCF	chr2:51399160-51399310	HepG2	liver:	n/a	n/a
33	CTCF	chr2:51474571-51474598	LNCaP	prostate:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
34	CTCF	chr2:51474540-51474690	HCT-116	colon:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
35	CTCF	chr2:51474501-51474692	Gliobla	brain:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
36	CTCF	chr2:51455939-51455997	GM20000	blood:	n/a	n/a
37	CTCF	chr2:51389925-51390081	GM12878	blood:	n/a	n/a
38	CTCF	chr2:51474540-51474690	HEK293	kidney:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
39	CTCF	chr2:51373952-51373975	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr2:51474460-51474610	NB4	blood:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
41	CTCF	chr2:51474538-51474660	MCF-7	breast:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
42	CTCF	chr2:51474573-51474627	MCF-7	breast:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
43	CTCF	chr2:51474200-51474350	HepG2	liver:	n/a	n/a
44	CTCF	chr2:51431722-51431746	GM20000	blood:	n/a	n/a
45	CTCF	chr2:51474561-51474645	H1-hESC	embryonic stem cell:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
46	CUX1	chr2:51439433-51439440	GM12878	blood:	n/a	n/a
47	CUX1	chr2:51431162-51431168	GM12878	blood:	n/a	n/a
48	E2F4	chr2:51384024-51384260	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr2:51441537-51441615	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr2:51467814-51468014	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51378948-51378998	AG09309	skin:	n/a
2	chr2:51446925-51446975	NHBE	bronchial:	n/a
3	chr2:51446925-51446975	HepG2	liver:	n/a
4	chr2:51446925-51446975	HIPEpiC	eye:	n/a
5	chr2:51446925-51446975	HL-60	blood:	n/a
6	chr2:51446925-51446975	PFSK-1	brain:	n/a
7	chr2:51446925-51446975	PANC-1	pancreas:	n/a
8	chr2:51378948-51378998	NHBE	bronchial:	n/a
9	chr2:51378948-51378998	HRCEpiC	kidney:	n/a
10	chr2:51379080-51379130	NB4	blood:	n/a
11	chr2:51379080-51379130	HIPEpiC	eye:	n/a
12	chr2:51379080-51379130	NH-A	brain:	n/a
13	chr2:51378948-51378998	NB4	blood:	n/a
14	chr2:51378948-51378998	H1-hESC	embryonic stem cell:	embryo
15	chr2:51379080-51379130	BJ	skin:	n/a
16	chr2:51378948-51378998	HCT-116	colon:	n/a
17	chr2:51379080-51379130	HRCEpiC	kidney:	n/a
18	chr2:51379080-51379130	HRPEpiC	eye:	n/a
19	chr2:51446925-51446975	SKMC	muscle:	n/a
20	chr2:51379080-51379130	PANC-1	pancreas:	n/a
21	chr2:51378948-51378998	HAEpiC	amniotic membrane:	n/a
22	chr2:51379080-51379130	NHDF-neo	bronchial:	n/a
23	chr2:51378948-51378998	SAEC	small airway:	n/a
24	chr2:51379080-51379130	HEEpiC	esophagus:	n/a
25	chr2:51446925-51446975	HEK293	kidney:	embryo
26	chr2:51378948-51378998	GM12892	blood:	n/a
27	chr2:51446925-51446975	AG04450	lung:	fetal
28	chr2:51446925-51446975	SAEC	small airway:	n/a
29	chr2:51446925-51446975	Caco-2	colon:	n/a
30	chr2:51378948-51378998	SKMC	muscle:	n/a
31	chr2:51379080-51379130	ProgFib	skin:	n/a
32	chr2:51379080-51379130	NHBE	bronchial:	n/a
33	chr2:51446925-51446975	GM12878	blood:	n/a
34	chr2:51378948-51378998	PFSK-1	brain:	n/a
35	chr2:51446925-51446975	K562	blood:	n/a
36	chr2:51378948-51378998	NT2-D1	testis:	n/a
37	chr2:51378948-51378998	A549	lung:	n/a
38	chr2:51379080-51379130	Jurkat	blood:	n/a
39	chr2:51446925-51446975	AG09309	skin:	n/a
40	chr2:51446925-51446975	NHDF-neo	bronchial:	n/a
41	chr2:51446925-51446975	U87	brain:	n/a
42	chr2:51379080-51379130	GM12891	blood:	n/a
43	chr2:51446925-51446975	AG10803	skin:	n/a
44	chr2:51446925-51446975	GM12891	blood:	n/a
45	chr2:51446925-51446975	HRCEpiC	kidney:	n/a
46	chr2:51378948-51378998	SK-N-MC	brain:	n/a
47	chr2:51446925-51446975	HEEpiC	esophagus:	n/a
48	chr2:51379080-51379130	GM12892	blood:	n/a
49	chr2:51379080-51379130	SK-N-SH_RA	brain:	n/a
50	chr2:51446925-51446975	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
2	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
3	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
4	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:
5	chr2:51395839..51397846-chr2:51399820..51401986,2	K562	blood:
6	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-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
3	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
4	lnc-NRXN1-4	chr2:51423222-51423493	l_1834_chr2:51413303-51423493_76bGuttman_hLF
5	lnc-NRXN1-4	chr2:51414157-51414291	l_1834_chr2:51413303-51423493_76bGuttman_hLF
6	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
7	lnc-NRXN1-1	chr2:51430129-51430286	ENSG00000237374
8	lnc-NRXN1-4	chr2:51413304-51413539	l_1834_chr2:51413303-51423493_76bGuttman_hLF
9	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374

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

Extended variants
information (count: 1821 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1821 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538360558	chr2:51372610-51372611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374313664	chr2:51372613-51372614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530119434	chr2:51372614-51372615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556350314	chr2:51372625-51372626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368223694	chr2:51372659-51372660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550386555	chr2:51372696-51372697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78975369	chr2:51372715-51372716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538789693	chr2:51372753-51372754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72830225	chr2:51372760-51372761	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs182142154	chr2:51372781-51372782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138332770	chr2:51372783-51372784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559253565	chr2:51372806-51372807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571278364	chr2:51372810-51372811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533740694	chr2:51372819-51372820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554577189	chr2:51372943-51372944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187202912	chr2:51373004-51373005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543518542	chr2:51373008-51373009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538526706	chr2:51373046-51373047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367799764	chr2:51373050-51373051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532075380	chr2:51373069-51373070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191624670	chr2:51373070-51373071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79404798	chr2:51373130-51373131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184714570	chr2:51373188-51373189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549386329	chr2:51373203-51373204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs202136222	chr2:51373234-51373235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150421369	chr2:51373242-51373243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561352797	chr2:51373252-51373253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573715134	chr2:51373291-51373292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116373862	chr2:51373311-51373312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550254214	chr2:51373326-51373327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541065158	chr2:51373340-51373341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72830226	chr2:51373414-51373415	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs4474919	chr2:51373443-51373444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576110222	chr2:51373452-51373453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539123398	chr2:51373555-51373556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138075545	chr2:51373667-51373668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200239104	chr2:51373668-51373669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564804845	chr2:51373723-51373724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189951326	chr2:51373783-51373784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565854271	chr2:51373828-51373829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573199234	chr2:51373831-51373832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372402363	chr2:51373834-51373835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112118993	chr2:51373863-51373864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs199697304	chr2:51373867-51373868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200668861	chr2:51373871-51373872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543917285	chr2:51373966-51373967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536569464	chr2:51373978-51373979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112923012	chr2:51373990-51373991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs137865200	chr2:51373999-51374000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185476259	chr2:51374000-51374001	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Bladder cancer	21909424	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51372600-51374000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:51377000-51379600	Weak transcription	Right Atrium	heart
3	chr2:51377200-51377600	Enhancers	Brain Germinal Matrix	brain
4	chr2:51377600-51382600	Weak transcription	Brain Germinal Matrix	brain
5	chr2:51378800-51379000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr2:51378800-51379400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:51380000-51381800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:51380200-51380600	Enhancers	Fetal Muscle Leg	muscle
9	chr2:51380400-51380800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:51380400-51381600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr2:51380400-51381600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr2:51382600-51383400	Enhancers	Brain Germinal Matrix	brain
13	chr2:51392600-51393400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:51392600-51393600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr2:51392600-51393600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:51392800-51393200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:51392800-51393400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr2:51392800-51393400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr2:51392800-51393600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:51392800-51393600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr2:51392800-51393800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr2:51393000-51393400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:51393000-51393400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr2:51393000-51393400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr2:51393000-51393400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr2:51393000-51393400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:51393000-51393600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:51393000-51393600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:51393400-51399800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr2:51393600-51396600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:51393600-51397200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr2:51393600-51397400	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr2:51396600-51397600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:51397200-51397800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:51397400-51397800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:51397400-51397800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr2:51397600-51398600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:51398600-51398800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:51435800-51436000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr2:51436600-51436800	Enhancers	Pancreas	Pancrea
41	chr2:51438800-51439000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr2:51439600-51439800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr2:51440800-51441600	Enhancers	NH-A	brain
44	chr2:51441600-51445600	Weak transcription	NH-A	brain
45	chr2:51443800-51444200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:51445600-51447400	Enhancers	NH-A	brain
47	chr2:51446200-51448000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr2:51446400-51446800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:51446400-51448000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:51446400-51448000	Enhancers	Cortex derived primary cultured neurospheres	brain

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