Variant report

Variant	nsv875194
Chromosome Location	chr2:141391918-141504719
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	ATF3	chr2:141401202-141401730	A549	lung:	n/a	n/a
2	BACH1	chr2:141454048-141454388	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:141500415-141500556	GM12878	blood:	n/a	chr2:141500477-141500488
4	BATF	chr2:141397290-141397464	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:141397275-141397515	GM12878	blood:	n/a	n/a
6	BCL3	chr2:141401061-141401908	A549	lung:	n/a	n/a
7	BCL3	chr2:141412222-141412454	GM12878	blood:	n/a	chr2:141412251-141412260
8	BCL3	chr2:141408265-141408853	A549	lung:	n/a	n/a
9	BHLHE40	chr2:141397346-141397363	GM12878	blood:	n/a	n/a
10	BRCA1	chr2:141406045-141406476	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr2:141401208-141401734	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr2:141452720-141453189	HCT-116	colon:	n/a	n/a
13	CCNT2	chr2:141438605-141438793	K562	blood:	n/a	n/a
14	CEBPB	chr2:141496419-141496669	IMR90	lung:	n/a	chr2:141496544-141496555
15	CEBPB	chr2:141438069-141438295	A549	lung:	n/a	chr2:141438204-141438215 chr2:141438204-141438217
16	CEBPB	chr2:141412904-141413446	A549	lung:	n/a	chr2:141413158-141413169
17	CEBPB	chr2:141412955-141414108	Hela-S3	cervix:	n/a	chr2:141413719-141413730 chr2:141413158-141413169 chr2:141414049-141414060 chr2:141414049-141414060
18	CEBPB	chr2:141436168-141436280	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:141401229-141401773	A549	lung:	n/a	n/a
20	CEBPB	chr2:141415225-141415654	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:141405992-141406254	MCF-7	breast:	n/a	chr2:141406061-141406072
22	CEBPB	chr2:141413012-141413302	IMR90	lung:	n/a	chr2:141413158-141413169
23	CEBPB	chr2:141408256-141408836	A549	lung:	n/a	chr2:141408555-141408567
24	CEBPB	chr2:141481596-141481809	A549	lung:	n/a	chr2:141481674-141481685 chr2:141481674-141481685
25	CEBPB	chr2:141436115-141436374	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:141456315-141456644	HepG2	liver:	n/a	chr2:141456478-141456489
27	CEBPB	chr2:141405969-141406271	MCF-7	breast:	n/a	chr2:141406061-141406072
28	CEBPB	chr2:141419274-141419355	A549	lung:	n/a	n/a
29	CEBPB	chr2:141438025-141438380	HepG2	liver:	n/a	chr2:141438284-141438296 chr2:141438204-141438215 chr2:141438204-141438217
30	CEBPB	chr2:141472162-141472375	A549	lung:	n/a	chr2:141472226-141472237 chr2:141472228-141472239 chr2:141472226-141472239 chr2:141472228-141472239 chr2:141472226-141472239
31	CEBPB	chr2:141472122-141472420	IMR90	lung:	n/a	chr2:141472226-141472237 chr2:141472228-141472239 chr2:141472226-141472239 chr2:141472228-141472239 chr2:141472226-141472239
32	CEBPB	chr2:141452735-141453068	IMR90	lung:	n/a	n/a
33	CEBPB	chr2:141452764-141453058	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:141496414-141496722	HepG2	liver:	n/a	chr2:141496544-141496555
35	CEBPB	chr2:141456328-141456626	A549	lung:	n/a	chr2:141456478-141456489
36	CEBPB	chr2:141401203-141401617	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:141438136-141438309	K562	blood:	n/a	chr2:141438284-141438296 chr2:141438204-141438215 chr2:141438204-141438217
38	CEBPB	chr2:141472069-141472416	HepG2	liver:	n/a	chr2:141472226-141472237 chr2:141472228-141472239 chr2:141472226-141472239 chr2:141472228-141472239 chr2:141472226-141472239
39	CEBPB	chr2:141401022-141401934	A549	lung:	n/a	n/a
40	CEBPB	chr2:141405888-141406511	Hela-S3	cervix:	n/a	chr2:141406061-141406072
41	CEBPB	chr2:141438062-141438277	H1-hESC	embryonic stem cell:	n/a	chr2:141438204-141438215 chr2:141438204-141438217
42	CEBPB	chr2:141436092-141436417	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:141484675-141484912	HepG2	liver:	n/a	chr2:141484756-141484765 chr2:141484756-141484765 chr2:141484754-141484767 chr2:141484756-141484765 chr2:141484755-141484766 chr2:141484756-141484765 chr2:141484754-141484765
44	CEBPB	chr2:141472155-141472465	Hela-S3	cervix:	n/a	chr2:141472226-141472237 chr2:141472228-141472239 chr2:141472226-141472239 chr2:141472228-141472239 chr2:141472226-141472239
45	CEBPB	chr2:141400511-141400650	HepG2	liver:	n/a	chr2:141400602-141400613
46	CEBPB	chr2:141422561-141422890	HepG2	liver:	n/a	chr2:141422733-141422742 chr2:141422733-141422742 chr2:141422733-141422744 chr2:141422733-141422742 chr2:141422731-141422742 chr2:141422733-141422742
47	CEBPB	chr2:141422596-141422881	A549	lung:	n/a	chr2:141422733-141422742 chr2:141422733-141422742 chr2:141422733-141422744 chr2:141422733-141422742 chr2:141422731-141422742 chr2:141422733-141422742
48	CEBPB	chr2:141401225-141401656	A549	lung:	n/a	n/a
49	CEBPB	chr2:141438056-141438368	IMR90	lung:	n/a	chr2:141438284-141438296 chr2:141438204-141438215 chr2:141438204-141438217
50	CEBPB	chr2:141452510-141453235	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:141441479-141441529	AG10803	skin:	n/a
2	chr2:141441479-141441529	GM12891	blood:	n/a
3	chr2:141441408-141441458	BJ	skin:	n/a
4	chr2:141441408-141441458	HL-60	blood:	n/a
5	chr2:141441408-141441458	HCT-116	colon:	n/a
6	chr2:141441408-141441458	PANC-1	pancreas:	n/a
7	chr2:141441479-141441529	ECC-1	luminal epithelium:	n/a
8	chr2:141441408-141441458	GM12892	blood:	n/a
9	chr2:141441408-141441458	HEEpiC	esophagus:	n/a
10	chr2:141441479-141441529	HAEpiC	amniotic membrane:	n/a
11	chr2:141441479-141441529	GM06990	blood:	n/a
12	chr2:141441408-141441458	HNPCEpiC	eye:	n/a
13	chr2:141441408-141441458	GM19239	blood:	n/a
14	chr2:141441408-141441458	NH-A	brain:	n/a
15	chr2:141441408-141441458	AG04450	lung:	fetal
16	chr2:141441479-141441529	LNCaP	prostate:	n/a
17	chr2:141441479-141441529	SK-N-SH_RA	brain:	n/a
18	chr2:141441479-141441529	GM19239	blood:	n/a
19	chr2:141441408-141441458	NB4	blood:	n/a
20	chr2:141441408-141441458	MCF10A-Er-Src	breast:	n/a
21	chr2:141441408-141441458	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:141441408-141441458	GM12891	blood:	n/a
23	chr2:141441479-141441529	HUVEC	blood vessel:	n/a
24	chr2:141441479-141441529	AoSMC	blood vessel:	n/a
25	chr2:141441479-141441529	HCPEpiC	choroid plexus:	n/a
26	chr2:141441408-141441458	U87	brain:	n/a
27	chr2:141441408-141441458	ProgFib	skin:	n/a
28	chr2:141441479-141441529	NHDF-neo	bronchial:	n/a
29	chr2:141441479-141441529	T-47D	breast:	n/a
30	chr2:141441408-141441458	HCM	heart:	n/a
31	chr2:141441408-141441458	ovcar-3	ovarian:	n/a
32	chr2:141441479-141441529	SK-N-MC	brain:	n/a
33	chr2:141441479-141441529	NB4	blood:	n/a
34	chr2:141441408-141441458	Hela-S3	cervix:	n/a
35	chr2:141441408-141441458	A549	lung:	n/a
36	chr2:141441479-141441529	U87	brain:	n/a
37	chr2:141441408-141441458	LNCaP	prostate:	n/a
38	chr2:141441408-141441458	PrEC	prostate:	n/a
39	chr2:141441408-141441458	RPTEC	kidney:	n/a
40	chr2:141441479-141441529	Hepatocyte	liver:	n/a
41	chr2:141441408-141441458	GM06990	blood:	n/a
42	chr2:141441408-141441458	HepG2	liver:	n/a
43	chr2:141441408-141441458	ECC-1	luminal epithelium:	n/a
44	chr2:141441408-141441458	HUVEC	blood vessel:	n/a
45	chr2:141441479-141441529	HRPEpiC	eye:	n/a
46	chr2:141441408-141441458	SK-N-MC	brain:	n/a
47	chr2:141441408-141441458	IMR90	lung:	fetal
48	chr2:141441479-141441529	BJ	skin:	n/a
49	chr2:141441408-141441458	Hepatocyte	liver:	n/a
50	chr2:141441408-141441458	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:141497933..141498923-chr2:141566337..141567066,2	MCF-7	breast:
2	chr2:141422971..141423545-chr20:53166808..53167673,2	MCF-7	breast:
3	chr2:141432163..141433732-chr2:141435544..141437895,2	MCF-7	breast:
4	chr2:141466926..141469105-chr2:141480476..141482979,2	MCF-7	breast:
5	chr2:141425529..141427088-chr2:141449758..141451483,2	MCF-7	breast:
6	chr2:141469791..141471888-chr2:141475142..141477938,2	MCF-7	breast:
7	chr2:141425529..141427088-chr2:141449758..141451483,2	MCF-7	breast:
8	chr2:141432163..141433732-chr2:141435544..141437895,2	MCF-7	breast:
9	chr2:141466926..141469105-chr2:141480476..141482979,2	MCF-7	breast:
10	chr2:141462311..141465013-chr2:141470003..141471554,2	K562	blood:
11	chr2:141469791..141471888-chr2:141475142..141477938,2	MCF-7	breast:
12	chr2:141503402..141505492-chr2:141538809..141541757,2	K562	blood:
13	chr2:141462311..141465013-chr2:141470003..141471554,2	K562	blood:

Variant related genes	Relation type
ENSG00000236440	TF binding region
ENSG00000236440	CpG island

Extended variants
information (count: 1624 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1624 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542952609	chr2:141396832-141396833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181119950	chr2:141396854-141396855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141897309	chr2:141396862-141396863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545238830	chr2:141396865-141396866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565045692	chr2:141396866-141396867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146046663	chr2:141396882-141396883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184492615	chr2:141396939-141396940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566898773	chr2:141396950-141396951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370495706	chr2:141396951-141396952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529271058	chr2:141396997-141396998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549295749	chr2:141397044-141397045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569441151	chr2:141397045-141397046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539610003	chr2:141397089-141397090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115602316	chr2:141397091-141397092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557954289	chr2:141397108-141397109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140049321	chr2:141397120-141397121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143894133	chr2:141397175-141397176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553580113	chr2:141397215-141397216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76108882	chr2:141397224-141397225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189065009	chr2:141397229-141397230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556159797	chr2:141397230-141397231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542684010	chr2:141397233-141397234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146404294	chr2:141397253-141397254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545275975	chr2:141397267-141397268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372570577	chr2:141397311-141397312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565083631	chr2:141397312-141397313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527485870	chr2:141397315-141397316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139769157	chr2:141397344-141397345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560362732	chr2:141397378-141397379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182518743	chr2:141397379-141397380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555844876	chr2:141397385-141397386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548983165	chr2:141397475-141397476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568884740	chr2:141397487-141397488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531888745	chr2:141397501-141397502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551620751	chr2:141397585-141397586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187104207	chr2:141397628-141397629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368747093	chr2:141397729-141397730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190682165	chr2:141397783-141397784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201198286	chr2:141397792-141397793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111432268	chr2:141397797-141397798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567262776	chr2:141397807-141397808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536323677	chr2:141397820-141397821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112476048	chr2:141397852-141397853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs794039	chr2:141397854-141397855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs372282105	chr2:141397924-141397925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558571045	chr2:141397938-141397939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs13431943	chr2:141397946-141397947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs70988414	chr2:141397982-141397983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs501737	chr2:141397990-141397991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540854039	chr2:141398025-141398026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma	21080181	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Autism	22543975	CNVD
Cancer	20164920	CNVD
Hypertension	22686481	CNVD
Hypospadia	22686481	CNVD
Intellectual disability	22686481	CNVD
Omphalocele	22686481	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141396800-141397600	Enhancers	Fetal Lung	lung
2	chr2:141397200-141397400	Enhancers	GM12878-XiMat	blood
3	chr2:141397600-141398400	Weak transcription	GM12878-XiMat	blood
4	chr2:141397600-141401200	Weak transcription	Fetal Lung	lung
5	chr2:141398400-141398600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr2:141398400-141399200	Enhancers	GM12878-XiMat	blood
7	chr2:141398400-141401000	Enhancers	A549	lung
8	chr2:141398600-141399200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:141398600-141401400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:141398800-141399200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:141399000-141399200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:141399000-141402000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr2:141399200-141399400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr2:141399200-141400800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:141399200-141401200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:141400800-141401200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:141400800-141402400	Enhancers	Hela-S3	cervix
18	chr2:141401000-141401200	Flanking Active TSS	A549	lung
19	chr2:141401000-141401400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr2:141401000-141401400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr2:141401000-141401600	Enhancers	HSMM	muscle
22	chr2:141401200-141401400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr2:141401200-141401400	Enhancers	NH-A	brain
24	chr2:141401200-141401600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr2:141401200-141401600	Enhancers	Fetal Lung	lung
26	chr2:141401200-141401600	Enhancers	HSMMtube	muscle
27	chr2:141401200-141401600	Active TSS	NHDF-Ad	bronchial
28	chr2:141401200-141401800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:141401200-141401800	Active TSS	A549	lung
30	chr2:141401200-141402000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:141401200-141402200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr2:141401400-141401600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:141401400-141401600	Flanking Active TSS	NH-A	brain
34	chr2:141401400-141401800	Active TSS	Muscle Satellite Cultured Cells	--
35	chr2:141401400-141401800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr2:141401400-141401800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr2:141401400-141401800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
38	chr2:141401600-141401800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr2:141401600-141401800	Active TSS	NH-A	brain
40	chr2:141401600-141402000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:141401600-141402200	Enhancers	Fetal Muscle Leg	muscle
42	chr2:141401800-141402200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr2:141401800-141402200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr2:141401800-141402400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr2:141401800-141402400	Flanking Active TSS	A549	lung
46	chr2:141402000-141402400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:141402400-141402800	Enhancers	A549	lung
48	chr2:141402400-141406200	Weak transcription	Hela-S3	cervix
49	chr2:141402400-141408000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:141402800-141406200	Weak transcription	A549	lung

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