Variant report

Variant	nsv873897
Chromosome Location	chr2:40139250-40225253
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	chr2:40140743-40141194	HepG2	liver:	n/a	n/a
2	ATF1	chr2:40223765-40224372	K562	blood:	n/a	n/a
3	ATF1	chr2:40222613-40222712	K562	blood:	n/a	n/a
4	ATF1	chr2:40217162-40217725	K562	blood:	n/a	n/a
5	BACH1	chr2:40208471-40208655	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:40149983-40150021	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr2:40140740-40141114	GM12878	blood:	n/a	n/a
8	CBX3	chr2:40223784-40224393	HCT-116	colon:	n/a	n/a
9	CCNT2	chr2:40224014-40224213	K562	blood:	n/a	n/a
10	CEBPB	chr2:40194850-40195177	HepG2	liver:	n/a	chr2:40195008-40195019
11	CEBPB	chr2:40194890-40195200	A549	lung:	n/a	chr2:40195008-40195019
12	CEBPB	chr2:40187059-40187300	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:40140744-40141140	Hela-S3	cervix:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
14	CEBPB	chr2:40223679-40224438	HCT-116	colon:	n/a	n/a
15	CEBPB	chr2:40140795-40141098	K562	blood:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
16	CEBPB	chr2:40218494-40218859	IMR90	lung:	n/a	chr2:40218674-40218685
17	CEBPB	chr2:40140796-40141140	A549	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
18	CEBPB	chr2:40223859-40224267	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:40223865-40224375	HCT-116	colon:	n/a	n/a
20	CEBPB	chr2:40223962-40224177	A549	lung:	n/a	n/a
21	CEBPB	chr2:40218529-40218785	HepG2	liver:	n/a	chr2:40218674-40218685
22	CEBPB	chr2:40218547-40218785	A549	lung:	n/a	chr2:40218674-40218685
23	CEBPB	chr2:40140766-40141153	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
24	CEBPB	chr2:40218557-40218771	H1-hESC	embryonic stem cell:	n/a	chr2:40218674-40218685
25	CEBPB	chr2:40194909-40195167	H1-hESC	embryonic stem cell:	n/a	chr2:40195008-40195019
26	CEBPB	chr2:40140785-40141280	IMR90	lung:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
27	CEBPB	chr2:40144232-40144363	A549	lung:	n/a	n/a
28	CEBPB	chr2:40140745-40141199	MCF-7	breast:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
29	CEBPB	chr2:40223752-40224243	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:40187092-40187228	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:40221391-40221660	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:40194970-40195037	K562	blood:	n/a	chr2:40195008-40195019
33	CEBPB	chr2:40157413-40157574	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:40140765-40141163	H1-hESC	embryonic stem cell:	n/a	chr2:40140980-40140993 chr2:40140982-40140993 chr2:40140982-40140993
35	CHD1	chr2:40140686-40141899	IMR90	lung:	n/a	n/a
36	CHD2	chr2:40223919-40224266	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr2:40140840-40140990	GM12870	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
38	CTCF	chr2:40140800-40140950	AG09319	gingival:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
39	CTCF	chr2:40140779-40141004	GM10248	blood:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
40	CTCF	chr2:40140780-40140930	AoAF	blood vessel:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
41	CTCF	chr2:40190220-40190370	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr2:40140440-40140590	GM12870	blood:	n/a	n/a
43	CTCF	chr2:40140841-40140936	MCF-7	breast:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
44	CTCF	chr2:40140774-40141021	Pancreas_OC	pancreas:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
45	CTCF	chr2:40140860-40141010	HCT-116	colon:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
46	CTCF	chr2:40140760-40141018	Lung_OC	lung:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
47	CTCF	chr2:40141100-40141250	AG04450	lung:	n/a	n/a
48	CTCF	chr2:40140602-40141162	HCT-116	colon:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
49	CTCF	chr2:40140818-40140968	A549	lung:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916
50	CTCF	chr2:40140800-40140950	HA-sp	spinal cord:	n/a	chr2:40140898-40140906 chr2:40140893-40140911 chr2:40140895-40140916

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40149258-40149308	PrEC	prostate:	n/a
2	chr2:40140929-40140979	Caco-2	colon:	n/a
3	chr2:40203342-40203392	HRE	kidney:	n/a
4	chr2:40147801-40147851	NT2-D1	testis:	n/a
5	chr2:40149258-40149308	GM12891	blood:	n/a
6	chr2:40203342-40203392	ProgFib	skin:	n/a
7	chr2:40140929-40140979	PFSK-1	brain:	n/a
8	chr2:40147801-40147851	GM12891	blood:	n/a
9	chr2:40140929-40140979	NT2-D1	testis:	n/a
10	chr2:40165558-40165608	BE2_C	brain:	n/a
11	chr2:40165558-40165608	HL-60	blood:	n/a
12	chr2:40149258-40149308	GM12892	blood:	n/a
13	chr2:40147801-40147851	Jurkat	blood:	n/a
14	chr2:40203342-40203392	T-47D	breast:	n/a
15	chr2:40140929-40140979	A549	lung:	n/a
16	chr2:40140929-40140979	MCF10A-Er-Src	breast:	n/a
17	chr2:40203342-40203392	GM19239	blood:	n/a
18	chr2:40149258-40149308	GM12878	blood:	n/a
19	chr2:40149258-40149308	HL-60	blood:	n/a
20	chr2:40147801-40147851	SK-N-SH	brain:	n/a
21	chr2:40165558-40165608	HNPCEpiC	eye:	n/a
22	chr2:40165558-40165608	AG04449	skin:	fetal
23	chr2:40147801-40147851	HEEpiC	esophagus:	n/a
24	chr2:40140929-40140979	U87	brain:	n/a
25	chr2:40140929-40140979	HCF	heart:	n/a
26	chr2:40147801-40147851	GM12892	blood:	n/a
27	chr2:40147801-40147851	ovcar-3	ovarian:	n/a
28	chr2:40147801-40147851	NHDF-neo	bronchial:	n/a
29	chr2:40165558-40165608	HUVEC	blood vessel:	n/a
30	chr2:40147801-40147851	Hela-S3	cervix:	n/a
31	chr2:40165558-40165608	LNCaP	prostate:	n/a
32	chr2:40147801-40147851	HCPEpiC	choroid plexus:	n/a
33	chr2:40165558-40165608	GM06990	blood:	n/a
34	chr2:40149258-40149308	NHBE	bronchial:	n/a
35	chr2:40147801-40147851	IMR90	lung:	fetal
36	chr2:40203342-40203392	HRCEpiC	kidney:	n/a
37	chr2:40147801-40147851	AG04449	skin:	fetal
38	chr2:40140929-40140979	GM12891	blood:	n/a
39	chr2:40140929-40140979	PrEC	prostate:	n/a
40	chr2:40165558-40165608	ProgFib	skin:	n/a
41	chr2:40203342-40203392	SK-N-SH	brain:	n/a
42	chr2:40165558-40165608	PANC-1	pancreas:	n/a
43	chr2:40147801-40147851	ECC-1	luminal epithelium:	n/a
44	chr2:40203342-40203392	SKMC	muscle:	n/a
45	chr2:40165558-40165608	GM19239	blood:	n/a
46	chr2:40147801-40147851	HIPEpiC	eye:	n/a
47	chr2:40165558-40165608	AoSMC	blood vessel:	n/a
48	chr2:40203342-40203392	PrEC	prostate:	n/a
49	chr2:40149258-40149308	GM06990	blood:	n/a
50	chr2:40140929-40140979	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:40140915..40141986-chr2:40781509..40782393,3	MCF-7	breast:
2	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
3	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
4	chr2:40140525..40141334-chr2:42009019..42009970,2	K562	blood:
5	chr2:40144153..40146237-chr2:40148819..40150420,2	K562	blood:
6	chr2:40140455..40141410-chr2:40986765..40987805,5	MCF-7	breast:
7	chr2:40140709..40141329-chr2:40986882..40987436,2	MCF-7	breast:
8	chr2:40140472..40141253-chr2:40471871..40472400,2	MCF-7	breast:
9	chr2:40164512..40166990-chr2:40173493..40175018,2	MCF-7	breast:
10	chr2:40004496..40006686-chr2:40138159..40140367,2	MCF-7	breast:
11	chr2:40140445..40141319-chr2:41925707..41926458,2	K562	blood:
12	chr2:39991894..39993577-chr2:40151910..40153730,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM178-2	chr2:40185553-40185606	ucscGeneNc_uc002rrw_2
2	lnc-TMEM178-2	chr2:40144774-40144799	NONHSAT070261
3	lnc-TMEM178-2	chr2:40149989-40150029	ENSG00000227028.1
4	lnc-TMEM178-2	chr2:40149990-40150029	NONHSAT070263
5	lnc-TMEM178-2	chr2:40149989-40150029	NONHSAT070261
6	lnc-TMEM178-2	chr2:40146833-40146923	ENSG00000227028.1

Variant related genes	Relation type
ENSG00000235653	TF binding region
SLC8A1-AS1	TF binding region
ENSG00000235653	CpG island
SLC8A1-AS1	CpG island
ENSG00000138050	chromatin interactions

Extended variants
information (count: 4783 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4783 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10185103	chr2:40139250-40139251	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184356933	chr2:40139284-40139285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs539705589	chr2:40139299-40139300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7568751	chr2:40139303-40139304	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs72932951	chr2:40139338-40139339	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536483798	chr2:40139349-40139350	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554943347	chr2:40139354-40139355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs372958226	chr2:40139379-40139380	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145525533	chr2:40139381-40139382	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565244712	chr2:40139385-40139386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115206132	chr2:40139395-40139396	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544718150	chr2:40139402-40139403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs7568665	chr2:40139406-40139407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs529896393	chr2:40139412-40139413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs557484213	chr2:40139416-40139417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs548391630	chr2:40139417-40139418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146524438	chr2:40139435-40139436	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs527545979	chr2:40139436-40139437	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552195915	chr2:40139441-40139442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570379362	chr2:40139527-40139528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537494735	chr2:40139558-40139559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189351716	chr2:40139595-40139596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567844033	chr2:40139612-40139613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535196472	chr2:40139633-40139634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555111656	chr2:40139662-40139663	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181226376	chr2:40139719-40139720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534460880	chr2:40139722-40139723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs149120094	chr2:40139753-40139754	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577304179	chr2:40139764-40139765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184215303	chr2:40139781-40139782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs556670957	chr2:40139825-40139826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs76581153	chr2:40139857-40139858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs72932954	chr2:40139862-40139863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs541406999	chr2:40139891-40139892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs560252978	chr2:40139900-40139901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11694888	chr2:40139908-40139909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12712663	chr2:40139911-40139912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs77518204	chr2:40139923-40139924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531186142	chr2:40139986-40139987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs370223514	chr2:40140105-40140106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs72932955	chr2:40140115-40140116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs557436681	chr2:40140126-40140127	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1541563	chr2:40140136-40140137	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1541562	chr2:40140139-40140140	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs188891236	chr2:40140164-40140165	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143020689	chr2:40140205-40140206	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs62137223	chr2:40140225-40140226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374102081	chr2:40140235-40140236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534165592	chr2:40140258-40140259	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114313707	chr2:40140288-40140289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40136200-40140600	Weak transcription	Dnd41	blood
2	chr2:40138400-40150400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr2:40138400-40150800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:40138600-40141000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:40139400-40140000	Enhancers	Thymus	Thymus
6	chr2:40140000-40141000	Weak transcription	Thymus	Thymus
7	chr2:40140000-40141800	Enhancers	Fetal Thymus	thymus
8	chr2:40140600-40141400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:40140600-40146800	Enhancers	Dnd41	blood
10	chr2:40141000-40141200	Flanking Active TSS	Fetal Lung	lung
11	chr2:40141000-40141200	Active TSS	Stomach Smooth Muscle	stomach
12	chr2:40141000-40141400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr2:40141000-40141400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr2:40141000-40141400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:40141000-40141400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:40141000-40141400	Enhancers	Colon Smooth Muscle	Colon
17	chr2:40141000-40141400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr2:40141000-40141400	Enhancers	Fetal Brain Male	brain
19	chr2:40141000-40141400	Enhancers	Fetal Intestine Small	intestine
20	chr2:40141000-40141400	Enhancers	Fetal Muscle Leg	muscle
21	chr2:40141000-40141400	Enhancers	Left Ventricle	heart
22	chr2:40141000-40141400	Enhancers	Pancreas	Pancrea
23	chr2:40141000-40141400	Enhancers	HMEC	breast
24	chr2:40141000-40141400	Enhancers	NH-A	brain
25	chr2:40141000-40141400	Enhancers	NHDF-Ad	bronchial
26	chr2:40141000-40141400	Enhancers	NHLF	lung
27	chr2:40141000-40141600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr2:40141000-40141600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:40141000-40141600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr2:40141000-40141600	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr2:40141000-40141600	Enhancers	Fetal Heart	heart
32	chr2:40141000-40141600	Enhancers	Ovary	ovary
33	chr2:40141000-40141600	Enhancers	HSMMtube	muscle
34	chr2:40141000-40141600	Enhancers	Osteobl	bone
35	chr2:40141000-40141800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:40141000-40141800	Enhancers	Fetal Kidney	kidney
37	chr2:40141000-40141800	Enhancers	Thymus	Thymus
38	chr2:40141000-40141800	Enhancers	HSMM	muscle
39	chr2:40141000-40142000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr2:40141000-40142000	Enhancers	Rectal Smooth Muscle	rectum
41	chr2:40141000-40142200	Enhancers	Fetal Stomach	stomach
42	chr2:40141200-40141400	Enhancers	Fetal Lung	lung
43	chr2:40141200-40141400	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr2:40141400-40141600	Flanking Active TSS	Colon Smooth Muscle	Colon
45	chr2:40141400-40141600	Enhancers	Stomach Smooth Muscle	stomach
46	chr2:40141400-40141800	Weak transcription	Fetal Lung	lung
47	chr2:40141400-40143000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr2:40141600-40144800	Weak transcription	Ovary	ovary
49	chr2:40141600-40145400	Weak transcription	HSMMtube	muscle
50	chr2:40141600-40164800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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