Variant report

Variant	nsv457886
Chromosome Location	chr2:53722595-53835083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:631)
CpG islands
(count:427)
Chromatin interactive
region (count:28)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:53786595-53787107	HCT-116	colon:	n/a	n/a
2	ATF3	chr2:53786715-53787135	HCT-116	colon:	n/a	n/a
3	BATF	chr2:53743872-53744174	GM12878	blood:	n/a	n/a
4	BATF	chr2:53743884-53744091	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:53788428-53788646	HepG2	liver:	n/a	n/a
6	BRCA1	chr2:53739626-53739837	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr2:53789639-53789689	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr2:53786689-53787220	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr2:53732954-53733393	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr2:53786670-53787211	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:53804310-53804615	K562	blood:	n/a	chr2:53804453-53804464
12	CEBPB	chr2:53795612-53795942	HepG2	liver:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
13	CEBPB	chr2:53725295-53725758	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr2:53786770-53787081	HepG2	liver:	n/a	chr2:53786937-53786948
15	CEBPB	chr2:53795617-53795967	ECC-1	luminal epithelium:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
16	CEBPB	chr2:53832665-53832917	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:53795600-53796008	A549	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
18	CEBPB	chr2:53789569-53789929	IMR90	lung:	n/a	chr2:53789749-53789760
19	CEBPB	chr2:53784458-53784658	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:53804303-53804543	HepG2	liver:	n/a	chr2:53804453-53804464
21	CEBPB	chr2:53752634-53752730	K562	blood:	n/a	n/a
22	CEBPB	chr2:53781633-53781847	HepG2	liver:	n/a	chr2:53781767-53781778
23	CEBPB	chr2:53786629-53787116	MCF-7	breast:	n/a	chr2:53786937-53786948
24	CEBPB	chr2:53786757-53787084	A549	lung:	n/a	chr2:53786937-53786948
25	CEBPB	chr2:53821343-53821832	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:53804321-53804582	IMR90	lung:	n/a	chr2:53804453-53804464
27	CEBPB	chr2:53789661-53789917	H1-hESC	embryonic stem cell:	n/a	chr2:53789749-53789760
28	CEBPB	chr2:53786518-53787262	HCT-116	colon:	n/a	chr2:53786937-53786948
29	CEBPB	chr2:53739555-53739944	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:53725272-53725726	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:53795583-53795925	IMR90	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
32	CEBPB	chr2:53824394-53824714	HepG2	liver:	n/a	chr2:53824617-53824628 chr2:53824562-53824573 chr2:53824621-53824632 chr2:53824524-53824535 chr2:53824621-53824632
33	CEBPB	chr2:53795596-53795941	A549	lung:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
34	CEBPB	chr2:53789525-53790053	A549	lung:	n/a	chr2:53789749-53789760
35	CEBPB	chr2:53789584-53789940	A549	lung:	n/a	chr2:53789749-53789760
36	CEBPB	chr2:53786452-53787275	HCT-116	colon:	n/a	chr2:53786937-53786948
37	CEBPB	chr2:53786621-53787131	Hela-S3	cervix:	n/a	chr2:53786937-53786948
38	CEBPB	chr2:53742616-53743191	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:53786702-53787114	MCF-7	breast:	n/a	chr2:53786937-53786948
40	CEBPB	chr2:53789530-53789931	MCF-7	breast:	n/a	chr2:53789749-53789760
41	CEBPB	chr2:53789634-53789824	HepG2	liver:	n/a	chr2:53789749-53789760
42	CEBPB	chr2:53824449-53824637	Hela-S3	cervix:	n/a	chr2:53824617-53824628 chr2:53824562-53824573 chr2:53824621-53824632 chr2:53824524-53824535 chr2:53824621-53824632
43	CEBPB	chr2:53743586-53743649	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:53739537-53739943	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:53810690-53810961	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:53789566-53789937	HepG2	liver:	n/a	chr2:53789749-53789760
47	CEBPB	chr2:53789586-53789943	K562	blood:	n/a	chr2:53789749-53789760
48	CEBPB	chr2:53789527-53789962	Hela-S3	cervix:	n/a	chr2:53789749-53789760
49	CEBPB	chr2:53795589-53795907	ECC-1	luminal epithelium:	n/a	chr2:53795748-53795761 chr2:53795749-53795760 chr2:53795750-53795759
50	CEBPB	chr2:53789454-53789990	MCF-7	breast:	n/a	chr2:53789749-53789760

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53747541-53747591	H1-hESC	embryonic stem cell:	embryo
2	chr2:53747541-53747591	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:53803878-53803928	NH-A	brain:	n/a
4	chr2:53725202-53725252	MCF-7	breast:	n/a
5	chr2:53725202-53725252	Jurkat	blood:	n/a
6	chr2:53747541-53747591	HAEpiC	amniotic membrane:	n/a
7	chr2:53747541-53747591	MCF10A-Er-Src	breast:	n/a
8	chr2:53814261-53814311	RPTEC	kidney:	n/a
9	chr2:53803878-53803928	HUVEC	blood vessel:	n/a
10	chr2:53814537-53814587	AG10803	skin:	n/a
11	chr2:53731598-53731648	SK-N-SH	brain:	n/a
12	chr2:53731598-53731648	AG09319	gingival:	n/a
13	chr2:53814261-53814311	PFSK-1	brain:	n/a
14	chr2:53803878-53803928	H1-hESC	embryonic stem cell:	embryo
15	chr2:53731598-53731648	H1-hESC	embryonic stem cell:	embryo
16	chr2:53814261-53814311	HRE	kidney:	n/a
17	chr2:53803878-53803928	T-47D	breast:	n/a
18	chr2:53814537-53814587	AG09319	gingival:	n/a
19	chr2:53731598-53731648	GM12891	blood:	n/a
20	chr2:53814537-53814587	LNCaP	prostate:	n/a
21	chr2:53764920-53764970	A549	lung:	n/a
22	chr2:53747541-53747591	LNCaP	prostate:	n/a
23	chr2:53764920-53764970	HRPEpiC	eye:	n/a
24	chr2:53731598-53731648	GM19239	blood:	n/a
25	chr2:53764920-53764970	HIPEpiC	eye:	n/a
26	chr2:53814261-53814311	GM06990	blood:	n/a
27	chr2:53747541-53747591	GM12878	blood:	n/a
28	chr2:53731598-53731648	Hela-S3	cervix:	n/a
29	chr2:53814537-53814587	PANC-1	pancreas:	n/a
30	chr2:53803878-53803928	BJ	skin:	n/a
31	chr2:53764920-53764970	HepG2	liver:	n/a
32	chr2:53764920-53764970	MCF10A-Er-Src	breast:	n/a
33	chr2:53731598-53731648	RPTEC	kidney:	n/a
34	chr2:53764920-53764970	LNCaP	prostate:	n/a
35	chr2:53814537-53814587	HUVEC	blood vessel:	n/a
36	chr2:53747541-53747591	AG10803	skin:	n/a
37	chr2:53731598-53731648	AoSMC	blood vessel:	n/a
38	chr2:53803878-53803928	SK-N-SH_RA	brain:	n/a
39	chr2:53814537-53814587	NH-A	brain:	n/a
40	chr2:53725202-53725252	AG09309	skin:	n/a
41	chr2:53803878-53803928	SKMC	muscle:	n/a
42	chr2:53747541-53747591	HCT-116	colon:	n/a
43	chr2:53814261-53814311	HRCEpiC	kidney:	n/a
44	chr2:53764920-53764970	SAEC	small airway:	n/a
45	chr2:53814261-53814311	ovcar-3	ovarian:	n/a
46	chr2:53725202-53725252	SKMC	muscle:	n/a
47	chr2:53731598-53731648	PrEC	prostate:	n/a
48	chr2:53814537-53814587	HCM	heart:	n/a
49	chr2:53803878-53803928	HNPCEpiC	eye:	n/a
50	chr2:53725202-53725252	NHDF-neo	bronchial:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:53795938..53798218-chr2:53812190..53814681,2	K562	blood:
2	chr2:53802111..53805957-chr2:53807457..53810844,3	K562	blood:
3	chr2:53763474..53765231-chr2:53774418..53775976,2	K562	blood:
4	chr2:53763474..53765231-chr2:53774418..53775976,2	K562	blood:
5	chr2:53807910..53809861-chr2:53812392..53815157,2	K562	blood:
6	chr2:53720586..53722714-chr2:53727046..53728819,2	MCF-7	breast:
7	chr2:53796597..53798405-chr2:53800976..53803366,2	MCF-7	breast:
8	chr2:53807910..53809861-chr2:53812392..53815157,2	K562	blood:
9	chr2:53800207..53803097-chr2:53806024..53807990,2	K562	blood:
10	chr2:53771758..53774525-chr2:53776196..53777860,2	MCF-7	breast:
11	chr2:53725082..53727239-chr2:53732255..53735113,2	K562	blood:
12	chr2:53771758..53774525-chr2:53776196..53777860,2	MCF-7	breast:
13	chr2:53774246..53775776-chr2:53777337..53778910,2	K562	blood:
14	chr2:53718351..53720003-chr2:53723225..53725281,2	K562	blood:
15	chr2:53757085..53758831-chr2:53762624..53764865,2	K562	blood:
16	chr2:53791197..53793053-chr2:53794870..53797027,2	K562	blood:
17	chr2:53764669..53766504-chr2:53770937..53773630,2	K562	blood:
18	chr2:53791197..53793053-chr2:53794870..53797027,2	K562	blood:
19	chr2:53804711..53806458-chr2:53809800..53812091,2	MCF-7	breast:
20	chr2:53725082..53727239-chr2:53732255..53735113,2	K562	blood:
21	chr2:53802111..53805957-chr2:53807457..53810844,3	K562	blood:
22	chr2:53764669..53766504-chr2:53770937..53773630,2	K562	blood:
23	chr2:53800207..53803097-chr2:53806024..53807990,2	K562	blood:
24	chr2:53757085..53758831-chr2:53762624..53764865,2	K562	blood:
25	chr2:53780507..53782864-chr2:53992929..53994536,2	K562	blood:
26	chr2:53774246..53775776-chr2:53777337..53778910,2	K562	blood:
27	chr2:53720586..53722714-chr2:53727046..53728819,2	MCF-7	breast:
28	chr2:53804711..53806458-chr2:53809800..53812091,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR75-6	chr2:53831411-53831558	NONHSAT070689
2	lnc-GPR75-6	chr2:53833559-53833596	NONHSAT070690
3	lnc-GPR75-6	chr2:53831784-53832052	NONHSAT070690
4	lnc-GPR75-6	chr2:53831895-53832052	NONHSAT070689
5	lnc-GPR75-6	chr2:53830522-53830655	NONHSAT070689
6	lnc-GPR75-6	chr2:53833057-53833215	NONHSAT070689
7	lnc-GPR75-6	chr2:53833057-53833217	NONHSAT070690
8	lnc-GPR75-6	chr2:53808341-53808515	NONHSAT070689

No data

Variant related genes	Relation type
RNU6-997P	TF binding region
GPR75-ASB3	TF binding region
RNU6-997P	CpG island
GPR75-ASB3	CpG island
ENSG00000207456	chromatin interactions

Extended variants
information (count: 4430 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4430 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11900008	chr2:53722595-53722596	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs541936770	chr2:53722609-53722610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187288159	chr2:53722622-53722623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111539664	chr2:53722624-53722625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529176200	chr2:53722631-53722632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376225739	chr2:53722650-53722651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377367428	chr2:53722710-53722711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532060281	chr2:53722712-53722713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549305567	chr2:53722719-53722720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370873979	chr2:53722734-53722735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531202864	chr2:53722806-53722807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs193198311	chr2:53722820-53722821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74621189	chr2:53722856-53722857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115494148	chr2:53722859-53722860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75486172	chr2:53722880-53722881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145224964	chr2:53722939-53722940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545772814	chr2:53723000-53723001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76907116	chr2:53723020-53723021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556571728	chr2:53723021-53723022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116811976	chr2:53723069-53723070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545053280	chr2:53723111-53723112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147204657	chr2:53723147-53723148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572417578	chr2:53723152-53723153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184702640	chr2:53723153-53723154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560343845	chr2:53723198-53723199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139726753	chr2:53723227-53723228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189682622	chr2:53723291-53723292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113861732	chr2:53723308-53723309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531664676	chr2:53723398-53723399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538196633	chr2:53723403-53723404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551055151	chr2:53723405-53723406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115596499	chr2:53723428-53723429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527337243	chr2:53723442-53723443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10204173	chr2:53723509-53723510	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs567063888	chr2:53723514-53723515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10167973	chr2:53723530-53723531	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs556746092	chr2:53723533-53723534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570240656	chr2:53723549-53723550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181296121	chr2:53723605-53723606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145695276	chr2:53723659-53723660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199871718	chr2:53723690-53723691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183689255	chr2:53723706-53723707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535057720	chr2:53723715-53723716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568189289	chr2:53723716-53723717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575011890	chr2:53723727-53723728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542825228	chr2:53723730-53723731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530714398	chr2:53723750-53723751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs80028805	chr2:53723815-53723816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114309255	chr2:53723817-53723818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564685373	chr2:53723863-53723864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	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
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53718000-53724200	Weak transcription	Aorta	Aorta
2	chr2:53718200-53725200	Weak transcription	Brain Anterior Caudate	brain
3	chr2:53718200-53737600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:53718600-53723600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr2:53718600-53724200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:53718800-53724600	Weak transcription	Hela-S3	cervix
7	chr2:53720600-53723400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:53721600-53722800	Weak transcription	Pancreas	Pancrea
9	chr2:53721600-53724200	Weak transcription	Left Ventricle	heart
10	chr2:53722800-53723600	Enhancers	Pancreas	Pancrea
11	chr2:53723200-53727600	Enhancers	Colon Smooth Muscle	Colon
12	chr2:53723400-53723600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:53723600-53724000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr2:53723600-53724000	Weak transcription	Pancreas	Pancrea
15	chr2:53723600-53724400	Enhancers	Stomach Smooth Muscle	stomach
16	chr2:53724000-53724600	Enhancers	Pancreas	Pancrea
17	chr2:53724000-53725800	Enhancers	Ovary	ovary
18	chr2:53724000-53727600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:53724200-53724600	Enhancers	Esophagus	oesophagus
20	chr2:53724200-53724600	Enhancers	Left Ventricle	heart
21	chr2:53724200-53724600	Enhancers	Lung	lung
22	chr2:53724200-53724600	Enhancers	Right Atrium	heart
23	chr2:53724200-53724600	Enhancers	Right Ventricle	heart
24	chr2:53724200-53724800	Enhancers	Aorta	Aorta
25	chr2:53724200-53727600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr2:53724400-53724600	Flanking Active TSS	Stomach Smooth Muscle	stomach
27	chr2:53724400-53726200	Enhancers	Brain Angular Gyrus	brain
28	chr2:53724400-53726200	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr2:53724400-53726200	Enhancers	Rectal Smooth Muscle	rectum
30	chr2:53724600-53725400	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr2:53724600-53725800	Weak transcription	Pancreas	Pancrea
32	chr2:53724600-53726000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:53724600-53726000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:53724600-53726000	Weak transcription	Lung	lung
35	chr2:53724600-53726400	Weak transcription	Right Atrium	heart
36	chr2:53724600-53726400	Enhancers	Hela-S3	cervix
37	chr2:53724600-53727600	Enhancers	Stomach Smooth Muscle	stomach
38	chr2:53724800-53726000	Enhancers	Brain Substantia Nigra	brain
39	chr2:53724800-53726800	Weak transcription	Aorta	Aorta
40	chr2:53725000-53726200	Enhancers	Liver	Liver
41	chr2:53725000-53726400	Enhancers	Fetal Stomach	stomach
42	chr2:53725000-53726600	Enhancers	Brain Hippocampus Middle	brain
43	chr2:53725200-53725400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr2:53725200-53725400	Enhancers	NH-A	brain
45	chr2:53725200-53725800	Enhancers	Brain Cingulate Gyrus	brain
46	chr2:53725200-53726400	Enhancers	Brain Anterior Caudate	brain
47	chr2:53725200-53727600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr2:53725400-53725600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:53725400-53725800	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr2:53725400-53726400	Enhancers	Cortex derived primary cultured neurospheres	brain

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