Variant report

Variant	nsv581876
Chromosome Location	chr2:51401676-51490709
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	CEBPB	chr2:51445233-51445599	IMR90	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
4	CEBPB	chr2:51485548-51485789	ECC-1	luminal epithelium:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
5	CEBPB	chr2:51461638-51461868	IMR90	lung:	n/a	chr2:51461726-51461737
6	CEBPB	chr2:51485456-51485813	K562	blood:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
7	CEBPB	chr2:51485499-51485822	A549	lung:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
8	CEBPB	chr2:51485456-51485732	ECC-1	luminal epithelium:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
9	CEBPB	chr2:51445259-51445582	HepG2	liver:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
10	CEBPB	chr2:51485451-51485812	A549	lung:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
11	CEBPB	chr2:51485458-51485831	H1-hESC	embryonic stem cell:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
12	CEBPB	chr2:51445272-51445575	A549	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
13	CEBPB	chr2:51485449-51485821	Hela-S3	cervix:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
14	CEBPB	chr2:51430857-51430966	H1-hESC	embryonic stem cell:	n/a	chr2:51430918-51430929
15	CEBPB	chr2:51430799-51430988	HepG2	liver:	n/a	chr2:51430918-51430929
16	CEBPB	chr2:51485529-51485787	MCF-7	breast:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
17	CEBPB	chr2:51485448-51485831	IMR90	lung:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
18	CEBPB	chr2:51461597-51461861	A549	lung:	n/a	chr2:51461726-51461737
19	CEBPB	chr2:51430897-51430932	A549	lung:	n/a	chr2:51430918-51430929
20	CEBPB	chr2:51461631-51461892	HepG2	liver:	n/a	chr2:51461726-51461737
21	CEBPB	chr2:51447009-51447209	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr2:51445290-51445497	H1-hESC	embryonic stem cell:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
23	CEBPB	chr2:51485458-51485815	A549	lung:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
24	CEBPB	chr2:51485456-51485816	HepG2	liver:	n/a	chr2:51485628-51485645 chr2:51485631-51485642
25	CTCF	chr2:51405496-51405532	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr2:51474460-51474610	NB4	blood:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
27	CTCF	chr2:51474538-51474660	MCF-7	breast:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
28	CTCF	chr2:51474200-51474350	HepG2	liver:	n/a	n/a
29	CTCF	chr2:51474573-51474627	MCF-7	breast:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
30	CTCF	chr2:51474571-51474598	LNCaP	prostate:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
31	CTCF	chr2:51474545-51474665	HepG2	liver:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
32	CTCF	chr2:51474620-51474770	A549	lung:	n/a	n/a
33	CTCF	chr2:51474556-51474571	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr2:51404272-51404367	GM12878	blood:	n/a	n/a
35	CTCF	chr2:51431722-51431746	GM20000	blood:	n/a	n/a
36	CTCF	chr2:51474501-51474692	Gliobla	brain:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
37	CTCF	chr2:51474540-51474690	HCT-116	colon:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
38	CTCF	chr2:51474561-51474645	H1-hESC	embryonic stem cell:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
39	CTCF	chr2:51474540-51474690	HEK293	kidney:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
40	CTCF	chr2:51474540-51474690	WERI-Rb-1	eye:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
41	CTCF	chr2:51474520-51474670	BE2_C	brain:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
42	CTCF	chr2:51474504-51474628	HepG2	liver:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
43	CTCF	chr2:51474584-51474618	A549	lung:	n/a	n/a
44	CTCF	chr2:51474391-51474673	H1-hESC	embryonic stem cell:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
45	CTCF	chr2:51474480-51474630	Caco-2	colon:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
46	CTCF	chr2:51455939-51455997	GM20000	blood:	n/a	n/a
47	CTCF	chr2:51474480-51474630	BE2_C	brain:	n/a	chr2:51474574-51474595 chr2:51474580-51474596 chr2:51474579-51474597
48	CTCF	chr2:51468664-51468715	Lung_OC	lung:	n/a	n/a
49	CUX1	chr2:51439433-51439440	GM12878	blood:	n/a	n/a
50	CUX1	chr2:51431162-51431168	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51446925-51446975	NHBE	bronchial:	n/a
2	chr2:51446925-51446975	Hela-S3	cervix:	n/a
3	chr2:51446925-51446975	NB4	blood:	n/a
4	chr2:51446925-51446975	SK-N-SH_RA	brain:	n/a
5	chr2:51446925-51446975	HRPEpiC	eye:	n/a
6	chr2:51446925-51446975	BJ	skin:	n/a
7	chr2:51446925-51446975	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:51446925-51446975	BE2_C	brain:	n/a
9	chr2:51446925-51446975	LNCaP	prostate:	n/a
10	chr2:51446925-51446975	AG09309	skin:	n/a
11	chr2:51446925-51446975	PrEC	prostate:	n/a
12	chr2:51446925-51446975	AoSMC	blood vessel:	n/a
13	chr2:51446925-51446975	NHDF-neo	bronchial:	n/a
14	chr2:51446925-51446975	HNPCEpiC	eye:	n/a
15	chr2:51446925-51446975	RPTEC	kidney:	n/a
16	chr2:51446925-51446975	GM19239	blood:	n/a
17	chr2:51446925-51446975	K562	blood:	n/a
18	chr2:51446925-51446975	CMK	blood:	n/a
19	chr2:51446925-51446975	AG09319	gingival:	n/a
20	chr2:51446925-51446975	PFSK-1	brain:	n/a
21	chr2:51446925-51446975	GM12892	blood:	n/a
22	chr2:51446925-51446975	ProgFib	skin:	n/a
23	chr2:51446925-51446975	AG10803	skin:	n/a
24	chr2:51446925-51446975	MCF10A-Er-Src	breast:	n/a
25	chr2:51446925-51446975	NT2-D1	testis:	n/a
26	chr2:51446925-51446975	HUVEC	blood vessel:	n/a
27	chr2:51446925-51446975	HMEC	breast:	n/a
28	chr2:51446925-51446975	HRE	kidney:	n/a
29	chr2:51446925-51446975	HCT-116	colon:	n/a
30	chr2:51446925-51446975	SK-N-SH	brain:	n/a
31	chr2:51446925-51446975	Jurkat	blood:	n/a
32	chr2:51446925-51446975	SKMC	muscle:	n/a
33	chr2:51446925-51446975	HL-60	blood:	n/a
34	chr2:51446925-51446975	HCF	heart:	n/a
35	chr2:51446925-51446975	SAEC	small airway:	n/a
36	chr2:51446925-51446975	H1-hESC	embryonic stem cell:	embryo
37	chr2:51446925-51446975	AG04449	skin:	fetal
38	chr2:51446925-51446975	HepG2	liver:	n/a
39	chr2:51446925-51446975	HCPEpiC	choroid plexus:	n/a
40	chr2:51446925-51446975	A549	lung:	n/a
41	chr2:51446925-51446975	GM12878	blood:	n/a
42	chr2:51446925-51446975	GM12891	blood:	n/a
43	chr2:51446925-51446975	HEEpiC	esophagus:	n/a
44	chr2:51446925-51446975	AG04450	lung:	fetal
45	chr2:51446925-51446975	GM06990	blood:	n/a
46	chr2:51446925-51446975	PANC-1	pancreas:	n/a
47	chr2:51446925-51446975	Caco-2	colon:	n/a
48	chr2:51446925-51446975	HRCEpiC	kidney:	n/a
49	chr2:51446925-51446975	U87	brain:	n/a
50	chr2:51446925-51446975	ovcar-3	ovarian:	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	chr2:51437981..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	chr2:51429219-51429452	ENSG00000237374
3	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
4	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
5	lnc-NRXN1-4	chr2:51413304-51413539	l_1834_chr2:51413303-51423493_76bGuttman_hLF
6	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
7	lnc-NRXN1-4	chr2:51414157-51414291	l_1834_chr2:51413303-51423493_76bGuttman_hLF
8	lnc-NRXN1-1	chr2:51430129-51430286	ENSG00000237374
9	lnc-NRXN1-4	chr2:51423222-51423493	l_1834_chr2:51413303-51423493_76bGuttman_hLF

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

Extended variants
information (count: 1243 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1243 , 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	rs542565631	chr2:51413346-51413347	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs558262247	chr2:51413362-51413363	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs372219296	chr2:51413379-51413380	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs143705974	chr2:51413404-51413405	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs185861797	chr2:51413412-51413413	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs191011766	chr2:51413455-51413456	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs571964645	chr2:51413456-51413457	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs573835367	chr2:51413495-51413496	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs542349923	chr2:51414163-51414164	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs139281695	chr2:51414176-51414177	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs548968117	chr2:51414193-51414194	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs562354603	chr2:51414211-51414212	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs199561923	chr2:51414274-51414275	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs558953629	chr2:51423269-51423270	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs570758203	chr2:51423288-51423289	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs535145039	chr2:51423316-51423317	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs554161418	chr2:51423347-51423348	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs571962184	chr2:51423365-51423366	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs560111363	chr2:51423402-51423403	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs574168404	chr2:51423405-51423406	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs553174652	chr2:51423409-51423410	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs184835389	chr2:51423443-51423444	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs150720529	chr2:51423455-51423456	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs189733359	chr2:51423464-51423465	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs59589098	chr2:51423465-51423466	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs113629148	chr2:51423485-51423486	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs557294244	chr2:51423486-51423487	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs575569184	chr2:51423491-51423492	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs190457990	chr2:51429247-51429248	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs41468948	chr2:51429262-51429263	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs574664948	chr2:51429263-51429264	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs535784215	chr2:51429286-51429287	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs531341771	chr2:51429356-51429357	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs143733065	chr2:51429372-51429373	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs551437880	chr2:51429450-51429451	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs566151419	chr2:51430220-51430221	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs10176094	chr2:51430278-51430279	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs537147948	chr2:51435849-51435850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139941328	chr2:51435887-51435888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191290152	chr2:51435890-51435891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs13419616	chr2:51435908-51435909	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs567397333	chr2:51435934-51435935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376127642	chr2:51435936-51435937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143375538	chr2:51435986-51435987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183485798	chr2:51435998-51435999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35941079	chr2:51436629-51436630	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs567214385	chr2:51436635-51436636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140373425	chr2:51436662-51436663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555763682	chr2:51436666-51436667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573914380	chr2:51436671-51436672	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:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51435800-51436000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:51436600-51436800	Enhancers	Pancreas	Pancrea
3	chr2:51438800-51439000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:51439600-51439800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:51440800-51441600	Enhancers	NH-A	brain
6	chr2:51441600-51445600	Weak transcription	NH-A	brain
7	chr2:51443800-51444200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:51445600-51447400	Enhancers	NH-A	brain
9	chr2:51446200-51448000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr2:51446400-51446800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr2:51446400-51448000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:51446400-51448000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr2:51446400-51448200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr2:51446400-51448200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr2:51446600-51447000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:51446600-51448200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr2:51446600-51448200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr2:51446800-51447200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:51446800-51447800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:51446800-51448000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr2:51447000-51447400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:51447200-51448000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr2:51447600-51448000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:51447600-51448000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:51447800-51448200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr2:51448000-51448200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr2:51448000-51452200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:51450400-51450600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr2:51450600-51451200	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr2:51451200-51453200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr2:51451800-51452600	Enhancers	Adipose Nuclei	Adipose
32	chr2:51452200-51453000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr2:51452400-51452800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:51457600-51458800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr2:51458800-51459000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr2:51459000-51459600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:51464600-51466200	Enhancers	Liver	Liver
38	chr2:51466200-51471400	Weak transcription	Liver	Liver
39	chr2:51470600-51471000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr2:51470600-51471200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr2:51471200-51471600	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr2:51471400-51472000	Enhancers	Liver	Liver
43	chr2:51474000-51474400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr2:51474000-51475200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr2:51474400-51474800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:51474800-51475200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:51486800-51487000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:51487000-51490600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr2:51489600-51492000	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr2:51489800-51491600	Enhancers	HUES48 Cell Line	embryonic stem cell

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