Variant report

Variant	nsv537430
Chromosome Location	chr4:186990348-187056028
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	ATF1	chr4:187027151-187027480	K562	blood:	n/a	n/a
2	ATF2	chr4:187027166-187027483	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:187055315-187055866	GM12878	blood:	n/a	n/a
4	BACH1	chr4:187025719-187026243	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:187026701-187026862	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr4:187055418-187055866	GM12878	blood:	n/a	n/a
7	BATF	chr4:187055371-187055785	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:187055420-187055843	GM12878	blood:	n/a	n/a
9	BCL3	chr4:187055433-187055716	GM12878	blood:	n/a	n/a
10	BCLAF1	chr4:187055428-187055813	GM12878	blood:	n/a	n/a
11	BCLAF1	chr4:187055345-187055835	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:187055496-187055825	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:187039012-187039026	K562	blood:	n/a	n/a
14	CEBPB	chr4:187037900-187038225	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
15	CEBPB	chr4:187037847-187038225	ECC-1	luminal epithelium:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
16	CEBPB	chr4:187037881-187038220	Hela-S3	cervix:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
17	CEBPB	chr4:187037849-187038207	ECC-1	luminal epithelium:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
18	CEBPB	chr4:187037872-187038236	IMR90	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
19	CEBPB	chr4:186990084-186990532	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:187037859-187038158	MCF-7	breast:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
21	CEBPB	chr4:187037867-187038233	HepG2	liver:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
22	CEBPB	chr4:187037845-187038266	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
23	CEBPB	chr4:187037868-187038236	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
24	CEBPB	chr4:187037865-187038243	K562	blood:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
25	CEBPB	chr4:187037874-187038237	H1-hESC	embryonic stem cell:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
26	CEBPB	chr4:187009826-187010155	HepG2	liver:	n/a	chr4:187009905-187009916
27	CHD1	chr4:187026105-187026212	H1-hESC	embryonic stem cell:	n/a	chr4:187026142-187026152
28	CHD2	chr4:187002365-187002951	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr4:187000118-187000352	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr4:187055449-187055790	GM12878	blood:	n/a	n/a
31	CTBP2	chr4:187025588-187026455	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr4:187026320-187026470	GM12866	blood:	n/a	n/a
33	CTCF	chr4:187054080-187054230	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr4:187054120-187054270	GM12869	blood:	n/a	n/a
35	CTCF	chr4:187054120-187054270	GM12867	blood:	n/a	n/a
36	CTCF	chr4:187054160-187054310	Caco-2	colon:	n/a	n/a
37	CTCF	chr4:187026160-187026310	GM12873	blood:	n/a	n/a
38	CTCF	chr4:187054124-187054308	GM12892	blood:	n/a	n/a
39	CTCF	chr4:187054180-187054330	A549	lung:	n/a	n/a
40	CTCF	chr4:187026340-187026490	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr4:187053900-187054050	HAc	cerebellar:	n/a	n/a
42	CTCF	chr4:187054104-187054331	HepG2	liver:	n/a	n/a
43	CTCF	chr4:187054160-187054310	GM12871	blood:	n/a	n/a
44	CTCF	chr4:187054160-187054310	GM12870	blood:	n/a	n/a
45	CTCF	chr4:187054155-187054279	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr4:187054200-187054350	RPTEC	kidney:	n/a	n/a
47	CTCF	chr4:187054100-187054250	GM12864	blood:	n/a	n/a
48	CTCF	chr4:187028775-187028877	GM10266	blood:	n/a	n/a
49	CTCF	chr4:187026340-187026490	GM12870	blood:	n/a	n/a
50	CTCF	chr4:187026220-187026370	GM12869	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:186990425-186990475	NB4	blood:	n/a
2	chr4:187039516-187039566	NT2-D1	testis:	n/a
3	chr4:186990324-186990374	GM12878	blood:	n/a
4	chr4:187039516-187039566	ovcar-3	ovarian:	n/a
5	chr4:186990425-186990475	NB4	blood:	n/a
6	chr4:187039516-187039566	NT2-D1	testis:	n/a
7	chr4:186990324-186990374	GM12878	blood:	n/a
8	chr4:187039516-187039566	ovcar-3	ovarian:	n/a
9	chr4:187025654-187025704	AG09319	gingival:	n/a
10	chr4:187026278-187026328	GM19239	blood:	n/a
11	chr4:187002617-187002667	T-47D	breast:	n/a
12	chr4:187002617-187002667	NH-A	brain:	n/a
13	chr4:186990324-186990374	A549	lung:	n/a
14	chr4:187013536-187013586	ovcar-3	ovarian:	n/a
15	chr4:187025897-187025947	AoSMC	blood vessel:	n/a
16	chr4:187026225-187026275	HIPEpiC	eye:	n/a
17	chr4:186990315-186990365	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:186990425-186990475	SKMC	muscle:	n/a
19	chr4:187026872-187026922	HL-60	blood:	n/a
20	chr4:187025420-187025470	BE2_C	brain:	n/a
21	chr4:187026278-187026328	NHBE	bronchial:	n/a
22	chr4:187003000-187003050	NHBE	bronchial:	n/a
23	chr4:187037318-187037368	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:187026278-187026328	HNPCEpiC	eye:	n/a
25	chr4:187025420-187025470	IMR90	lung:	fetal
26	chr4:187025654-187025704	RPTEC	kidney:	n/a
27	chr4:187002617-187002667	U87	brain:	n/a
28	chr4:187026278-187026328	HMEC	breast:	n/a
29	chr4:187003000-187003050	SKMC	muscle:	n/a
30	chr4:187026710-187026760	Hepatocyte	liver:	n/a
31	chr4:187053574-187053624	MCF-7	breast:	n/a
32	chr4:187026872-187026922	HRCEpiC	kidney:	n/a
33	chr4:187037318-187037368	SKMC	muscle:	n/a
34	chr4:187002617-187002667	Jurkat	blood:	n/a
35	chr4:187025420-187025470	HCM	heart:	n/a
36	chr4:187037318-187037368	GM12878	blood:	n/a
37	chr4:187000846-187000896	HL-60	blood:	n/a
38	chr4:187013536-187013586	IMR90	lung:	fetal
39	chr4:187003000-187003050	HRPEpiC	eye:	n/a
40	chr4:187026872-187026922	K562	blood:	n/a
41	chr4:187037256-187037306	GM12878	blood:	n/a
42	chr4:187025654-187025704	GM06990	blood:	n/a
43	chr4:187037256-187037306	HL-60	blood:	n/a
44	chr4:186990315-186990365	ECC-1	luminal epithelium:	n/a
45	chr4:186990324-186990374	Hela-S3	cervix:	n/a
46	chr4:187037318-187037368	MCF-7	breast:	n/a
47	chr4:187023193-187023243	HepG2	liver:	n/a
48	chr4:187002617-187002667	NT2-D1	testis:	n/a
49	chr4:187025886-187025936	AG10803	skin:	n/a
50	chr4:187023193-187023243	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
2	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
3	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
4	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
5	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
6	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
7	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
8	chr4:187023730..187026664-chr4:187030524..187032198,2	MCF-7	breast:
9	chr4:187021448..187022968-chr6:31674535..31677393,2	K562	blood:
10	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
11	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
12	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
13	chr4:187036166..187038039-chr4:187110587..187113537,2	K562	blood:

Variant related genes	Relation type
ENSG00000253013	TF binding region
FAM149A	TF binding region
TLR3	TF binding region
ENSG00000253013	CpG island
FAM149A	CpG island
TLR3	CpG island
ENSG00000145476	chromatin interactions
ENSG00000109794	chromatin interactions
ENSG00000204424	chromatin interactions
ENSG00000250641	chromatin interactions
ENSG00000269302	chromatin interactions

Extended variants
information (count: 2745 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2745 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138085273	chr4:186990349-186990350	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs546403644	chr4:186990385-186990386	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs5743310	chr4:186990393-186990394	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs373809349	chr4:186990435-186990436	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs539644579	chr4:186990444-186990445	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs556041380	chr4:186990457-186990458	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs377321123	chr4:186990478-186990479	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs181240423	chr4:186990517-186990518	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs367653100	chr4:186990567-186990568	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs555039956	chr4:186990596-186990597	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs571735232	chr4:186990770-186990771	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs540605849	chr4:186990790-186990791	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs201140940	chr4:186990821-186990822	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs564814276	chr4:186990829-186990830	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs75357674	chr4:186990842-186990843	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs185843080	chr4:186990883-186990884	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs149468333	chr4:186990887-186990888	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs143860912	chr4:186990932-186990933	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs78963230	chr4:186990948-186990949	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs559870654	chr4:186990986-186990987	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs528512736	chr4:186990987-186990988	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs551458109	chr4:186990998-186990999	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs189127426	chr4:186991001-186991002	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs574930011	chr4:186991044-186991045	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs539316099	chr4:186991055-186991056	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs116082889	chr4:186991086-186991087	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs569799248	chr4:186991126-186991127	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs11721827	chr4:186991137-186991138	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs555075662	chr4:186991175-186991176	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs571770333	chr4:186991251-186991252	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs140268652	chr4:186991284-186991285	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs11730143	chr4:186991302-186991303	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528998281	chr4:186991401-186991402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs578202898	chr4:186991406-186991407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543800141	chr4:186991421-186991422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563987656	chr4:186991454-186991455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574319532	chr4:186991455-186991456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543210170	chr4:186991504-186991505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571303218	chr4:186991518-186991519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201954120	chr4:186991524-186991525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79357622	chr4:186991529-186991530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182018233	chr4:186991530-186991531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74566553	chr4:186991533-186991534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142760491	chr4:186991540-186991541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530932546	chr4:186991600-186991601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs386683464	chr4:186991609-186991610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370824696	chr4:186991610-186991611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538294588	chr4:186991718-186991719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376691949	chr4:186991785-186991786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564938819	chr4:186991821-186991822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17086460	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1067 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186989000-186990800	Active TSS	Rectal Smooth Muscle	rectum
2	chr4:186989000-186991000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:186989000-186991000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:186989000-186991000	Active TSS	Right Atrium	heart
5	chr4:186989200-186990600	Active TSS	Primary T helper naive cells from peripheral blood	blood
6	chr4:186989200-186990800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:186989200-186990800	Active TSS	Brain Angular Gyrus	brain
8	chr4:186989200-186990800	Active TSS	Rectal Mucosa Donor 29	rectum
9	chr4:186989200-186990800	Active TSS	Stomach Smooth Muscle	stomach
10	chr4:186989200-186990800	Active TSS	NHLF	lung
11	chr4:186989200-186991000	Active TSS	Brain Cingulate Gyrus	brain
12	chr4:186989200-186991000	Active TSS	Duodenum Mucosa	Duodenum
13	chr4:186989200-186991000	Active TSS	Skeletal Muscle Male	skeletal muscle
14	chr4:186989200-186991200	Active TSS	Brain Anterior Caudate	brain
15	chr4:186989200-186991200	Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr4:186989200-186991200	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr4:186989200-186991200	Active TSS	Psoas Muscle	Psoas
18	chr4:186989200-187000600	Weak transcription	Spleen	Spleen
19	chr4:186989400-186990400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
20	chr4:186989400-186990600	Flanking Active TSS	Primary hematopoietic stem cells	blood
21	chr4:186989400-186990600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
22	chr4:186989400-186990600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr4:186989400-186990600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr4:186989400-186990600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:186989400-186990600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:186989400-186990600	Active TSS	Left Ventricle	heart
27	chr4:186989400-186990600	Active TSS	NH-A	brain
28	chr4:186989400-186990800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:186989400-186990800	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr4:186989400-186990800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:186989400-186991000	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr4:186989400-186991000	Active TSS	Muscle Satellite Cultured Cells	--
33	chr4:186989400-186991000	Active TSS	Aorta	Aorta
34	chr4:186989400-186991000	Active TSS	Colonic Mucosa	Colon
35	chr4:186989400-186991000	Active TSS	Esophagus	oesophagus
36	chr4:186989400-186991000	Active TSS	Stomach Mucosa	stomach
37	chr4:186989400-186991200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:186989400-186991200	Active TSS	Brain Hippocampus Middle	brain
39	chr4:186989400-186991200	Active TSS	Brain Substantia Nigra	brain
40	chr4:186989400-186991200	Active TSS	Colon Smooth Muscle	Colon
41	chr4:186989600-186990400	Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr4:186989600-186990400	Active TSS	Fetal Lung	lung
43	chr4:186989600-186990600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:186989600-186990600	Active TSS	Fetal Intestine Large	intestine
45	chr4:186989600-186990600	Active TSS	Fetal Muscle Trunk	muscle
46	chr4:186989600-186990600	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr4:186989600-186990600	Active TSS	A549	lung
48	chr4:186989600-186990600	Active TSS	Monocytes-CD14+_RO01746	blood
49	chr4:186989600-186990800	Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr4:186989600-186990800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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