Variant report

Variant	esv2830346
Chromosome Location	chr4:186983342-187044161
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	chr4:186989219-186989538	HepG2	liver:	n/a	n/a
2	ATF1	chr4:187027151-187027480	K562	blood:	n/a	n/a
3	ATF2	chr4:187027166-187027483	H1-hESC	embryonic stem cell:	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	BHLHE40	chr4:187039012-187039026	K562	blood:	n/a	n/a
7	CBX3	chr4:186989030-186989622	HCT-116	colon:	n/a	chr4:186989176-186989187
8	CEBPB	chr4:187037859-187038158	MCF-7	breast:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
9	CEBPB	chr4:187037881-187038220	Hela-S3	cervix:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
10	CEBPB	chr4:187037867-187038233	HepG2	liver:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
11	CEBPB	chr4:187037845-187038266	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
12	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
13	CEBPB	chr4:187037872-187038236	IMR90	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
14	CEBPB	chr4:186990084-186990532	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:187037865-187038243	K562	blood:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
16	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
17	CEBPB	chr4:187037868-187038236	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
18	CEBPB	chr4:187009826-187010155	HepG2	liver:	n/a	chr4:187009905-187009916
19	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
20	CEBPB	chr4:187037900-187038225	A549	lung:	n/a	chr4:187038050-187038059 chr4:187038050-187038059 chr4:187038048-187038061 chr4:187038050-187038059 chr4:187038048-187038059
21	CHD1	chr4:187026105-187026212	H1-hESC	embryonic stem cell:	n/a	chr4:187026142-187026152
22	CHD2	chr4:187002365-187002951	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr4:187000118-187000352	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr4:187025588-187026455	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr4:186989220-186989370	GM12866	blood:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366
26	CTCF	chr4:186989320-186989470	HEEpiC	esophagus:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
27	CTCF	chr4:186989280-186989430	HBMEC	blood vessel:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
28	CTCF	chr4:186989320-186989470	HFF	foreskin:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
29	CTCF	chr4:186989142-186989556	H1-hESC	embryonic stem cell:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
30	CTCF	chr4:187026160-187026310	HEK293	kidney:	n/a	n/a
31	CTCF	chr4:186989340-186989490	GM12873	blood:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
32	CTCF	chr4:186989260-186989410	Caco-2	colon:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
33	CTCF	chr4:186989238-186989487	Fibrobl	skin:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
34	CTCF	chr4:186989240-186989390	HPAF	blood vessel:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
35	CTCF	chr4:186989280-186989430	HFF-Myc	foreskin:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
36	CTCF	chr4:186989243-186989466	Hela-S3	cervix:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
37	CTCF	chr4:186989285-186989447	MCF-7	breast:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
38	CTCF	chr4:186989259-186989460	K562	blood:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
39	CTCF	chr4:187026200-187026350	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr4:186989300-186989450	NHDF-neo	bronchial:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
41	CTCF	chr4:186989320-186989470	AG04450	lung:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
42	CTCF	chr4:186989300-186989450	Hela-S3	cervix:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
43	CTCF	chr4:186989260-186989410	AoAF	blood vessel:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
44	CTCF	chr4:187025960-187026110	GM12867	blood:	n/a	n/a
45	CTCF	chr4:186989120-186989270	A549	lung:	n/a	n/a
46	CTCF	chr4:187018409-187018443	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:187026300-187026450	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr4:187026160-187026310	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr4:186989280-186989430	HPF	lung:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371
50	CTCF	chr4:186989280-186989430	BJ	skin:	n/a	chr4:186989349-186989365 chr4:186989351-186989364 chr4:186989348-186989366 chr4:186989350-186989371

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187002617-187002667	RPTEC	kidney:	n/a
2	chr4:187037318-187037368	AG09309	skin:	n/a
3	chr4:187026278-187026328	Jurkat	blood:	n/a
4	chr4:187002617-187002667	RPTEC	kidney:	n/a
5	chr4:187037318-187037368	AG09309	skin:	n/a
6	chr4:187026278-187026328	Jurkat	blood:	n/a
7	chr4:187026225-187026275	T-47D	breast:	n/a
8	chr4:186990006-186990056	GM06990	blood:	n/a
9	chr4:187026710-187026760	NB4	blood:	n/a
10	chr4:187003000-187003050	AG10803	skin:	n/a
11	chr4:187026278-187026328	HCT-116	colon:	n/a
12	chr4:187026710-187026760	HRPEpiC	eye:	n/a
13	chr4:187025897-187025947	T-47D	breast:	n/a
14	chr4:187000846-187000896	SK-N-SH	brain:	n/a
15	chr4:187023193-187023243	GM12892	blood:	n/a
16	chr4:187039516-187039566	AG10803	skin:	n/a
17	chr4:187026970-187027020	HepG2	liver:	n/a
18	chr4:187026225-187026275	K562	blood:	n/a
19	chr4:187000846-187000896	A549	lung:	n/a
20	chr4:187026872-187026922	AG09309	skin:	n/a
21	chr4:187003000-187003050	HEEpiC	esophagus:	n/a
22	chr4:186990324-186990374	AG09319	gingival:	n/a
23	chr4:187037256-187037306	CMK	blood:	n/a
24	chr4:186990315-186990365	MCF10A-Er-Src	breast:	n/a
25	chr4:187026710-187026760	Hepatocyte	liver:	n/a
26	chr4:187013536-187013586	NHBE	bronchial:	n/a
27	chr4:187037256-187037306	HAEpiC	amniotic membrane:	n/a
28	chr4:187026970-187027020	MCF-7	breast:	n/a
29	chr4:186990425-186990475	HepG2	liver:	n/a
30	chr4:187025886-187025936	Caco-2	colon:	n/a
31	chr4:187023193-187023243	AG04450	lung:	fetal
32	chr4:186990425-186990475	GM12878	blood:	n/a
33	chr4:187026225-187026275	HUVEC	blood vessel:	n/a
34	chr4:187037318-187037368	HMEC	breast:	n/a
35	chr4:187037256-187037306	HEK293	kidney:	embryo
36	chr4:187002617-187002667	Hepatocyte	liver:	n/a
37	chr4:187039516-187039566	SKMC	muscle:	n/a
38	chr4:187039516-187039566	SK-N-SH_RA	brain:	n/a
39	chr4:187037318-187037368	HCM	heart:	n/a
40	chr4:187026970-187027020	GM19239	blood:	n/a
41	chr4:186990006-186990056	HRCEpiC	kidney:	n/a
42	chr4:187013645-187013695	HCF	heart:	n/a
43	chr4:187013536-187013586	HEK293	kidney:	embryo
44	chr4:186990202-186990252	HCPEpiC	choroid plexus:	n/a
45	chr4:187003000-187003050	AG09319	gingival:	n/a
46	chr4:187026872-187026922	BJ	skin:	n/a
47	chr4:187013645-187013695	CMK	blood:	n/a
48	chr4:187025420-187025470	Caco-2	colon:	n/a
49	chr4:187023193-187023243	HUVEC	blood vessel:	n/a
50	chr4:187026970-187027020	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
2	chr4:186985477..186986987-chr4:187047828..187050010,2	K562	blood:
3	chr4:186988828..186989568-chr4:187053779..187054412,2	MCF-7	breast:
4	chr4:187036166..187038039-chr4:187110587..187113537,2	K562	blood:
5	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
6	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
7	chr4:186981542..186984257-chr4:186986669..186988190,2	MCF-7	breast:
8	chr4:187000465..187002106-chr4:187010501..187012706,2	MCF-7	breast:
9	chr4:187009172..187011759-chr4:187017494..187019918,3	K562	blood:
10	chr4:187023730..187026664-chr4:187030524..187032198,2	MCF-7	breast:
11	chr4:187002937..187005829-chr4:187012756..187015507,2	MCF-7	breast:
12	chr4:186988895..186989419-chr4:187058283..187058978,2	K562	blood:
13	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:
14	chr4:186988859..186989716-chr4:187058329..187059203,5	MCF-7	breast:
15	chr4:186981542..186984257-chr4:186986669..186988190,2	MCF-7	breast:
16	chr4:187021448..187022968-chr6:31674535..31677393,2	K562	blood:

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

Extended variants
information (count: 2565 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs956239	chr4:186983342-186983343	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140532287	chr4:186983352-186983353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370356825	chr4:186983373-186983374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79182785	chr4:186983400-186983401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138512083	chr4:186983401-186983402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143876298	chr4:186983405-186983406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369037432	chr4:186983414-186983415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146338367	chr4:186983433-186983434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183177244	chr4:186983441-186983442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560462701	chr4:186983487-186983488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577139818	chr4:186983491-186983492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs5864970	chr4:186983495-186983496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs397829384	chr4:186983503-186983504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546007370	chr4:186983518-186983519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562590035	chr4:186983521-186983522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78838153	chr4:186983527-186983528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531409549	chr4:186983604-186983605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7682198	chr4:186983605-186983606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs561685421	chr4:186983643-186983644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78263887	chr4:186983646-186983647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531677591	chr4:186983647-186983648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527281882	chr4:186983658-186983659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548500325	chr4:186983707-186983708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114254834	chr4:186983733-186983734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570786981	chr4:186983749-186983750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376098423	chr4:186983755-186983756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568314976	chr4:186983760-186983761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539677420	chr4:186983779-186983780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570073042	chr4:186983832-186983833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117375507	chr4:186983874-186983875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35979315	chr4:186983976-186983977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555484335	chr4:186984003-186984004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572441786	chr4:186984029-186984030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7658239	chr4:186984059-186984060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs554144354	chr4:186984085-186984086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577177087	chr4:186984088-186984089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7658550	chr4:186984115-186984116	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs187584726	chr4:186984124-186984125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563869292	chr4:186984177-186984178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138834982	chr4:186984180-186984181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561626752	chr4:186984223-186984224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149383225	chr4:186984233-186984234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553656606	chr4:186984252-186984253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540607734	chr4:186984295-186984296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34609719	chr4:186984310-186984311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs533418322	chr4:186984322-186984323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540977842	chr4:186984329-186984330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531230828	chr4:186984372-186984373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370822078	chr4:186984375-186984376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570188996	chr4:186984387-186984388	Weak transcription	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:1133 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186980200-186989200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr4:186985000-186989000	Weak transcription	Left Ventricle	heart
3	chr4:186986800-186987000	Enhancers	HepG2	liver
4	chr4:186987200-186987400	Enhancers	Brain Hippocampus Middle	brain
5	chr4:186987200-186988200	Enhancers	Brain Germinal Matrix	brain
6	chr4:186987200-186988800	Weak transcription	HepG2	liver
7	chr4:186987400-186989000	Weak transcription	Brain Hippocampus Middle	brain
8	chr4:186988200-186989400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:186988200-186989800	Weak transcription	Brain Germinal Matrix	brain
10	chr4:186988400-186988800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:186988400-186989200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr4:186988800-186989000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:186988800-186989000	Enhancers	Colon Smooth Muscle	Colon
14	chr4:186988800-186989200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:186988800-186989200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:186988800-186989200	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr4:186988800-186989200	Enhancers	HepG2	liver
18	chr4:186988800-186989200	Enhancers	NHDF-Ad	bronchial
19	chr4:186988800-186989400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr4:186988800-186989400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:186989000-186989200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:186989000-186989200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr4:186989000-186989200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
24	chr4:186989000-186989200	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr4:186989000-186989200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:186989000-186989200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:186989000-186989200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:186989000-186989200	Enhancers	Fetal Kidney	kidney
29	chr4:186989000-186989200	Enhancers	Fetal Lung	lung
30	chr4:186989000-186989200	Enhancers	Ovary	ovary
31	chr4:186989000-186989200	Enhancers	Pancreas	Pancrea
32	chr4:186989000-186989200	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr4:186989000-186989200	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr4:186989000-186989200	Enhancers	Spleen	Spleen
35	chr4:186989000-186989200	Enhancers	Dnd41	blood
36	chr4:186989000-186989200	Bivalent Enhancer	GM12878-XiMat	blood
37	chr4:186989000-186989200	Enhancers	Osteobl	bone
38	chr4:186989000-186989400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr4:186989000-186989400	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr4:186989000-186989400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr4:186989000-186989400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:186989000-186989400	Enhancers	Liver	Liver
43	chr4:186989000-186989400	Flanking Active TSS	Brain Hippocampus Middle	brain
44	chr4:186989000-186989400	Enhancers	Brain Substantia Nigra	brain
45	chr4:186989000-186989400	Flanking Active TSS	Colon Smooth Muscle	Colon
46	chr4:186989000-186989400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr4:186989000-186989400	Enhancers	Fetal Muscle Leg	muscle
48	chr4:186989000-186989400	Enhancers	Fetal Stomach	stomach
49	chr4:186989000-186989400	Enhancers	Left Ventricle	heart
50	chr4:186989000-186989400	Enhancers	Right Ventricle	heart

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