Variant report

Variant	nsv875195
Chromosome Location	chr2:141407101-141542081
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	ATF2	chr2:141505134-141505570	GM12878	blood:	n/a	n/a
2	ATF2	chr2:141505161-141505544	GM12878	blood:	n/a	n/a
3	BACH1	chr2:141454048-141454388	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:141519699-141519825	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:141505144-141505618	GM12878	blood:	n/a	chr2:141505391-141505402
6	BATF	chr2:141505260-141505548	GM12878	blood:	n/a	chr2:141505391-141505402
7	BATF	chr2:141500415-141500556	GM12878	blood:	n/a	chr2:141500477-141500488
8	BCL11A	chr2:141505208-141505580	GM12878	blood:	n/a	n/a
9	BCL3	chr2:141408265-141408853	A549	lung:	n/a	n/a
10	BCL3	chr2:141412222-141412454	GM12878	blood:	n/a	chr2:141412251-141412260
11	BCL3	chr2:141505239-141505520	GM12878	blood:	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	chr2:141438069-141438295	A549	lung:	n/a	chr2:141438204-141438215 chr2:141438204-141438217
15	CEBPB	chr2:141436115-141436374	IMR90	lung:	n/a	n/a
16	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
17	CEBPB	chr2:141472162-141472375	A549	lung:	n/a	chr2:141472226-141472237 chr2:141472228-141472239 chr2:141472226-141472239 chr2:141472228-141472239 chr2:141472226-141472239
18	CEBPB	chr2:141415225-141415654	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:141436092-141436417	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:141496414-141496722	HepG2	liver:	n/a	chr2:141496544-141496555
21	CEBPB	chr2:141472155-141472465	Hela-S3	cervix:	n/a	chr2:141472226-141472237 chr2:141472228-141472239 chr2:141472226-141472239 chr2:141472228-141472239 chr2:141472226-141472239
22	CEBPB	chr2:141494636-141494944	HepG2	liver:	n/a	n/a
23	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
24	CEBPB	chr2:141456329-141456621	IMR90	lung:	n/a	chr2:141456478-141456489
25	CEBPB	chr2:141456328-141456626	A549	lung:	n/a	chr2:141456478-141456489
26	CEBPB	chr2:141452591-141453111	HCT-116	colon:	n/a	n/a
27	CEBPB	chr2:141472069-141472416	HepG2	liver:	n/a	chr2:141472226-141472237 chr2:141472228-141472239 chr2:141472226-141472239 chr2:141472228-141472239 chr2:141472226-141472239
28	CEBPB	chr2:141452735-141453068	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:141413032-141413293	HepG2	liver:	n/a	chr2:141413158-141413169
30	CEBPB	chr2:141505246-141505665	GM12878	blood:	n/a	n/a
31	CEBPB	chr2:141413019-141413303	A549	lung:	n/a	chr2:141413158-141413169
32	CEBPB	chr2:141422574-141422887	IMR90	lung:	n/a	chr2:141422733-141422742 chr2:141422733-141422742 chr2:141422733-141422744 chr2:141422733-141422742 chr2:141422731-141422742 chr2:141422733-141422742
33	CEBPB	chr2:141472122-141472420	IMR90	lung:	n/a	chr2:141472226-141472237 chr2:141472228-141472239 chr2:141472226-141472239 chr2:141472228-141472239 chr2:141472226-141472239
34	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
35	CEBPB	chr2:141452510-141453235	HCT-116	colon:	n/a	n/a
36	CEBPB	chr2:141408256-141408836	A549	lung:	n/a	chr2:141408555-141408567
37	CEBPB	chr2:141436201-141436313	K562	blood:	n/a	n/a
38	CEBPB	chr2:141438062-141438277	H1-hESC	embryonic stem cell:	n/a	chr2:141438204-141438215 chr2:141438204-141438217
39	CEBPB	chr2:141412955-141414108	Hela-S3	cervix:	n/a	chr2:141413719-141413730 chr2:141413158-141413169 chr2:141414049-141414060 chr2:141414049-141414060
40	CEBPB	chr2:141438136-141438309	K562	blood:	n/a	chr2:141438284-141438296 chr2:141438204-141438215 chr2:141438204-141438217
41	CEBPB	chr2:141456315-141456644	HepG2	liver:	n/a	chr2:141456478-141456489
42	CEBPB	chr2:141438025-141438380	HepG2	liver:	n/a	chr2:141438284-141438296 chr2:141438204-141438215 chr2:141438204-141438217
43	CEBPB	chr2:141452680-141453086	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr2:141517066-141517393	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr2:141419274-141419355	A549	lung:	n/a	n/a
46	CEBPB	chr2:141413028-141413295	A549	lung:	n/a	chr2:141413158-141413169
47	CEBPB	chr2:141481596-141481809	A549	lung:	n/a	chr2:141481674-141481685 chr2:141481674-141481685
48	CEBPB	chr2:141412904-141413446	A549	lung:	n/a	chr2:141413158-141413169
49	CEBPB	chr2:141436083-141436351	A549	lung:	n/a	n/a
50	CEBPB	chr2:141436168-141436280	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:141441479-141441529	U87	brain:	n/a
2	chr2:141441479-141441529	SK-N-MC	brain:	n/a
3	chr2:141441479-141441529	HRE	kidney:	n/a
4	chr2:141441408-141441458	HUVEC	blood vessel:	n/a
5	chr2:141441479-141441529	A549	lung:	n/a
6	chr2:141441479-141441529	PrEC	prostate:	n/a
7	chr2:141441479-141441529	HRPEpiC	eye:	n/a
8	chr2:141441479-141441529	HCT-116	colon:	n/a
9	chr2:141441408-141441458	HEK293	kidney:	embryo
10	chr2:141441408-141441458	AG04449	skin:	fetal
11	chr2:141441408-141441458	NHDF-neo	bronchial:	n/a
12	chr2:141441408-141441458	HMEC	breast:	n/a
13	chr2:141441408-141441458	NHBE	bronchial:	n/a
14	chr2:141441479-141441529	HAEpiC	amniotic membrane:	n/a
15	chr2:141441479-141441529	RPTEC	kidney:	n/a
16	chr2:141441408-141441458	AG10803	skin:	n/a
17	chr2:141441479-141441529	MCF10A-Er-Src	breast:	n/a
18	chr2:141441479-141441529	AG10803	skin:	n/a
19	chr2:141441479-141441529	AG04449	skin:	fetal
20	chr2:141441408-141441458	NT2-D1	testis:	n/a
21	chr2:141441479-141441529	PANC-1	pancreas:	n/a
22	chr2:141441479-141441529	MCF-7	breast:	n/a
23	chr2:141441479-141441529	CMK	blood:	n/a
24	chr2:141441479-141441529	HNPCEpiC	eye:	n/a
25	chr2:141441408-141441458	SK-N-SH_RA	brain:	n/a
26	chr2:141441408-141441458	HCM	heart:	n/a
27	chr2:141441479-141441529	Hepatocyte	liver:	n/a
28	chr2:141441408-141441458	SK-N-MC	brain:	n/a
29	chr2:141441479-141441529	HCPEpiC	choroid plexus:	n/a
30	chr2:141441479-141441529	HEEpiC	esophagus:	n/a
31	chr2:141441408-141441458	HRE	kidney:	n/a
32	chr2:141441408-141441458	RPTEC	kidney:	n/a
33	chr2:141441408-141441458	PFSK-1	brain:	n/a
34	chr2:141441479-141441529	K562	blood:	n/a
35	chr2:141441408-141441458	ovcar-3	ovarian:	n/a
36	chr2:141441479-141441529	SK-N-SH_RA	brain:	n/a
37	chr2:141441408-141441458	K562	blood:	n/a
38	chr2:141441408-141441458	AG09319	gingival:	n/a
39	chr2:141441479-141441529	LNCaP	prostate:	n/a
40	chr2:141441408-141441458	ProgFib	skin:	n/a
41	chr2:141441479-141441529	HepG2	liver:	n/a
42	chr2:141441408-141441458	Hela-S3	cervix:	n/a
43	chr2:141441479-141441529	HCM	heart:	n/a
44	chr2:141441408-141441458	BE2_C	brain:	n/a
45	chr2:141441479-141441529	IMR90	lung:	fetal
46	chr2:141441479-141441529	AG09309	skin:	n/a
47	chr2:141441408-141441458	Jurkat	blood:	n/a
48	chr2:141441408-141441458	HAEpiC	amniotic membrane:	n/a
49	chr2:141441479-141441529	PFSK-1	brain:	n/a
50	chr2:141441408-141441458	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:141503402..141505492-chr2:141538809..141541757,2	K562	blood:
2	chr2:141514849..141517014-chr2:141519451..141521522,2	MCF-7	breast:
3	chr2:141469791..141471888-chr2:141475142..141477938,2	MCF-7	breast:
4	chr2:141432163..141433732-chr2:141435544..141437895,2	MCF-7	breast:
5	chr2:141466926..141469105-chr2:141480476..141482979,2	MCF-7	breast:
6	chr2:141469791..141471888-chr2:141475142..141477938,2	MCF-7	breast:
7	chr2:141432163..141433732-chr2:141435544..141437895,2	MCF-7	breast:
8	chr2:141466926..141469105-chr2:141480476..141482979,2	MCF-7	breast:
9	chr2:141497933..141498923-chr2:141566337..141567066,2	MCF-7	breast:
10	chr2:141425529..141427088-chr2:141449758..141451483,2	MCF-7	breast:
11	chr2:141425529..141427088-chr2:141449758..141451483,2	MCF-7	breast:
12	chr2:141503402..141505492-chr2:141538809..141541757,2	K562	blood:
13	chr2:141536035..141538351-chr2:141538844..141542293,3	MCF-7	breast:
14	chr2:141536035..141538351-chr2:141538844..141542293,3	MCF-7	breast:
15	chr2:141462311..141465013-chr2:141470003..141471554,2	K562	blood:
16	chr2:141514849..141517014-chr2:141519451..141521522,2	MCF-7	breast:
17	chr2:141422971..141423545-chr20:53166808..53167673,2	MCF-7	breast:
18	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: 1807 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1807 , 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	rs4954847	chr2:141407101-141407102	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555298120	chr2:141407176-141407177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6709373	chr2:141407182-141407183	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs537135434	chr2:141407270-141407271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115030306	chr2:141407271-141407272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576890381	chr2:141407278-141407279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374948039	chr2:141407293-141407294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571465253	chr2:141407325-141407326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377119480	chr2:141407335-141407336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79436196	chr2:141407420-141407421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554070676	chr2:141407430-141407431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114325978	chr2:141407483-141407484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561659885	chr2:141407498-141407499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529322450	chr2:141407508-141407509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188463221	chr2:141407563-141407564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373458409	chr2:141407569-141407570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191262244	chr2:141407659-141407660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs503560	chr2:141407660-141407661	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs376870395	chr2:141407670-141407671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200577755	chr2:141407698-141407699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554244698	chr2:141407700-141407701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116046812	chr2:141407732-141407733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554961220	chr2:141407739-141407740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186769380	chr2:141407747-141407748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537316417	chr2:141407751-141407752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550689962	chr2:141407783-141407784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369128915	chr2:141407792-141407793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs577349061	chr2:141407799-141407800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115288461	chr2:141407826-141407827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs17497508	chr2:141407844-141407845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs199767953	chr2:141407878-141407879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371633576	chr2:141407879-141407880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372671872	chr2:141407885-141407886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200961804	chr2:141407886-141407887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111868554	chr2:141407888-141407889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112678665	chr2:141407900-141407901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112695975	chr2:141407904-141407905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191201839	chr2:141407908-141407909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184876854	chr2:141407936-141407937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561321113	chr2:141407957-141407958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530851617	chr2:141407958-141407959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs482286	chr2:141407976-141407977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs559590118	chr2:141407986-141407987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564334592	chr2:141408006-141408007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12151420	chr2:141408045-141408046	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs552745853	chr2:141408080-141408081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566185653	chr2:141408106-141408107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528547635	chr2:141408119-141408120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188747440	chr2:141408128-141408129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568427876	chr2:141408192-141408193	Enhancers 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:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141402400-141408000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:141406200-141407200	Enhancers	A549	lung
3	chr2:141406200-141407600	Enhancers	Hela-S3	cervix
4	chr2:141406200-141408200	Weak transcription	HUVEC	blood vessel
5	chr2:141407200-141408200	Weak transcription	A549	lung
6	chr2:141407600-141408000	Weak transcription	Hela-S3	cervix
7	chr2:141408000-141408200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:141408000-141408600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr2:141408000-141408600	Enhancers	Hela-S3	cervix
10	chr2:141408000-141408800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:141408200-141408800	Flanking Active TSS	A549	lung
12	chr2:141408200-141408800	Enhancers	HUVEC	blood vessel
13	chr2:141408600-141412200	Weak transcription	Hela-S3	cervix
14	chr2:141408800-141409200	Weak transcription	HUVEC	blood vessel
15	chr2:141408800-141410000	Enhancers	A549	lung
16	chr2:141409200-141409400	Enhancers	HUVEC	blood vessel
17	chr2:141409400-141413000	Weak transcription	HUVEC	blood vessel
18	chr2:141410000-141412000	Weak transcription	A549	lung
19	chr2:141411800-141412600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr2:141412000-141412400	Flanking Active TSS	A549	lung
21	chr2:141412000-141412600	Enhancers	Fetal Brain Female	brain
22	chr2:141412200-141412400	Enhancers	Hela-S3	cervix
23	chr2:141412400-141413000	Weak transcription	Hela-S3	cervix
24	chr2:141412400-141414000	Active TSS	A549	lung
25	chr2:141413000-141413200	Flanking Active TSS	HUVEC	blood vessel
26	chr2:141413000-141413800	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr2:141413000-141413800	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr2:141413000-141417400	Enhancers	Hela-S3	cervix
29	chr2:141413200-141413600	Active TSS	HUVEC	blood vessel
30	chr2:141413600-141413800	Flanking Active TSS	HUVEC	blood vessel
31	chr2:141413800-141417200	Enhancers	HUVEC	blood vessel
32	chr2:141414000-141416400	Enhancers	A549	lung
33	chr2:141414200-141418200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr2:141415400-141415600	Enhancers	Fetal Lung	lung
35	chr2:141416200-141417000	Enhancers	Fetal Kidney	kidney
36	chr2:141416400-141416600	Flanking Active TSS	A549	lung
37	chr2:141416600-141416800	Enhancers	A549	lung
38	chr2:141416800-141417400	Flanking Active TSS	A549	lung
39	chr2:141417000-141420800	Weak transcription	Fetal Kidney	kidney
40	chr2:141417400-141418000	Enhancers	A549	lung
41	chr2:141420400-141421200	Enhancers	Adipose Nuclei	Adipose
42	chr2:141420800-141421200	Enhancers	Fetal Kidney	kidney
43	chr2:141421200-141422000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr2:141422000-141424400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:141424000-141424800	Enhancers	Dnd41	blood
46	chr2:141424000-141425800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr2:141424400-141424800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:141424400-141425200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr2:141425800-141426400	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr2:141426400-141426600	Enhancers	Pancreatic Islets	Pancreatic Islet

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