Variant report

Variant	nsv427685
Chromosome Location	chr4:86032872-86340548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1918)
CpG islands
(count:244)
Chromatin interactive
region (count:40)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1918 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:86229331-86229442	K562	blood:	n/a	n/a
2	ATF2	chr4:86314364-86314746	GM12878	blood:	n/a	n/a
3	ATF2	chr4:86068585-86068976	GM12878	blood:	n/a	n/a
4	ATF2	chr4:86313067-86313597	GM12878	blood:	n/a	n/a
5	ATF2	chr4:86320454-86320960	GM12878	blood:	n/a	n/a
6	ATF2	chr4:86339259-86339697	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr4:86048684-86049181	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:86048845-86049075	K562	blood:	n/a	n/a
9	ATF3	chr4:86048748-86049111	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:86191038-86191060	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:86117184-86117484	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:86117223-86117513	K562	blood:	n/a	n/a
13	BACH1	chr4:86048880-86049071	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr4:86320395-86320834	GM12878	blood:	n/a	n/a
15	BATF	chr4:86314416-86314711	GM12878	blood:	n/a	n/a
16	BATF	chr4:86313227-86313498	GM12878	blood:	n/a	chr4:86313353-86313364
17	BATF	chr4:86314421-86314721	GM12878	blood:	n/a	n/a
18	BATF	chr4:86320360-86320837	GM12878	blood:	n/a	n/a
19	BATF	chr4:86063739-86064004	GM12878	blood:	n/a	n/a
20	BATF	chr4:86063742-86063931	GM12878	blood:	n/a	n/a
21	BATF	chr4:86313135-86313542	GM12878	blood:	n/a	chr4:86313353-86313364
22	BATF	chr4:86340374-86340600	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:86068628-86068932	HepG2	liver:	n/a	n/a
24	BHLHE40	chr4:86048848-86049072	K562	blood:	n/a	n/a
25	BHLHE40	chr4:86068614-86068984	K562	blood:	n/a	n/a
26	BHLHE40	chr4:86068600-86068994	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:86313291-86313386	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:86291752-86291834	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:86048861-86049039	HepG2	liver:	n/a	n/a
30	BRCA1	chr4:86192905-86192925	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr4:86315020-86315079	GM12878	blood:	n/a	n/a
32	BRCA1	chr4:86135175-86135202	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr4:86048765-86049237	HCT-116	colon:	n/a	n/a
34	CBX3	chr4:86117241-86117526	K562	blood:	n/a	n/a
35	CBX3	chr4:86048746-86049249	HCT-116	colon:	n/a	n/a
36	CBX3	chr4:86048769-86049126	K562	blood:	n/a	n/a
37	CBX3	chr4:86130228-86130740	HCT-116	colon:	n/a	chr4:86130519-86130530
38	CCNT2	chr4:86239533-86239580	K562	blood:	n/a	n/a
39	CEBPB	chr4:86250065-86250358	HepG2	liver:	n/a	chr4:86250287-86250300 chr4:86250207-86250218 chr4:86250317-86250330
40	CEBPB	chr4:86089605-86089943	HepG2	liver:	n/a	chr4:86089783-86089796 chr4:86089784-86089795
41	CEBPB	chr4:86120100-86120347	IMR90	lung:	n/a	chr4:86120180-86120191
42	CEBPB	chr4:86103845-86104147	HepG2	liver:	n/a	chr4:86103969-86103980
43	CEBPB	chr4:86048860-86049105	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:86250050-86250298	A549	lung:	n/a	chr4:86250207-86250218
45	CEBPB	chr4:86180598-86180746	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:86103877-86104138	K562	blood:	n/a	chr4:86103969-86103980
47	CEBPB	chr4:86250042-86250347	IMR90	lung:	n/a	chr4:86250287-86250300 chr4:86250207-86250218 chr4:86250317-86250330
48	CEBPB	chr4:86250058-86250323	H1-hESC	embryonic stem cell:	n/a	chr4:86250287-86250300 chr4:86250207-86250218
49	CEBPB	chr4:86303244-86303471	H1-hESC	embryonic stem cell:	n/a	chr4:86303339-86303350
50	CEBPB	chr4:86303163-86303514	HepG2	liver:	n/a	chr4:86303339-86303350

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:86224551-86224601	U87	brain:	n/a
2	chr4:86224551-86224601	SK-N-MC	brain:	n/a
3	chr4:86224551-86224601	AG09319	gingival:	n/a
4	chr4:86224551-86224601	HMEC	breast:	n/a
5	chr4:86224551-86224601	PFSK-1	brain:	n/a
6	chr4:86049133-86049183	HCF	heart:	n/a
7	chr4:86167447-86167497	HEK293	kidney:	embryo
8	chr4:86224551-86224601	BJ	skin:	n/a
9	chr4:86167398-86167448	AG04450	lung:	fetal
10	chr4:86049133-86049183	IMR90	lung:	fetal
11	chr4:86167447-86167497	NT2-D1	testis:	n/a
12	chr4:86167447-86167497	NHBE	bronchial:	n/a
13	chr4:86167398-86167448	IMR90	lung:	fetal
14	chr4:86167447-86167497	HL-60	blood:	n/a
15	chr4:86167398-86167448	GM12891	blood:	n/a
16	chr4:86167398-86167448	HAEpiC	amniotic membrane:	n/a
17	chr4:86049133-86049183	NHBE	bronchial:	n/a
18	chr4:86167447-86167497	PrEC	prostate:	n/a
19	chr4:86049133-86049183	GM12878	blood:	n/a
20	chr4:86049133-86049183	GM12891	blood:	n/a
21	chr4:86049133-86049183	HCT-116	colon:	n/a
22	chr4:86049133-86049183	H1-hESC	embryonic stem cell:	embryo
23	chr4:86167398-86167448	SAEC	small airway:	n/a
24	chr4:86167398-86167448	ProgFib	skin:	n/a
25	chr4:86049133-86049183	BJ	skin:	n/a
26	chr4:86167398-86167448	H1-hESC	embryonic stem cell:	embryo
27	chr4:86049133-86049183	AG04449	skin:	fetal
28	chr4:86167447-86167497	BJ	skin:	n/a
29	chr4:86224551-86224601	ovcar-3	ovarian:	n/a
30	chr4:86224551-86224601	HCM	heart:	n/a
31	chr4:86167447-86167497	PANC-1	pancreas:	n/a
32	chr4:86049133-86049183	ovcar-3	ovarian:	n/a
33	chr4:86167447-86167497	AG10803	skin:	n/a
34	chr4:86167398-86167448	SKMC	muscle:	n/a
35	chr4:86224551-86224601	SK-N-SH	brain:	n/a
36	chr4:86049133-86049183	AG09319	gingival:	n/a
37	chr4:86167447-86167497	SK-N-SH	brain:	n/a
38	chr4:86167447-86167497	Hela-S3	cervix:	n/a
39	chr4:86167447-86167497	H1-hESC	embryonic stem cell:	embryo
40	chr4:86049133-86049183	ECC-1	luminal epithelium:	n/a
41	chr4:86167447-86167497	HIPEpiC	eye:	n/a
42	chr4:86167398-86167448	MCF10A-Er-Src	breast:	n/a
43	chr4:86167447-86167497	IMR90	lung:	fetal
44	chr4:86167447-86167497	HEEpiC	esophagus:	n/a
45	chr4:86167447-86167497	AG04449	skin:	fetal
46	chr4:86167447-86167497	SAEC	small airway:	n/a
47	chr4:86167398-86167448	BJ	skin:	n/a
48	chr4:86224551-86224601	HRCEpiC	kidney:	n/a
49	chr4:86224551-86224601	HCT-116	colon:	n/a
50	chr4:86049133-86049183	SK-N-SH_RA	brain:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:86310843..86313430-chr4:86339747..86342570,2	K562	blood:
2	chr20:45985356..45987543-chr4:86157556..86159275,2	MCF-7	breast:
3	chr4:86006119..86008878-chr4:86034902..86037833,2	K562	blood:
4	chr4:86339378..86339952-chr4:86669138..86670126,2	MCF-7	breast:
5	chr4:86048857..86049411-chr4:86239183..86239916,2	MCF-7	breast:
6	chr4:86320129..86322866-chr4:86332900..86334770,2	K562	blood:
7	chr4:86164928..86165741-chr4:86291153..86292328,4	MCF-7	breast:
8	chr4:86068522..86069297-chr4:86668912..86669717,2	MCF-7	breast:
9	chr4:86070706..86072618-chr4:86075988..86078281,2	MCF-7	breast:
10	chr4:86234301..86236109-chr4:86239273..86242093,2	K562	blood:
11	chr4:86286749..86288574-chr4:86295386..86298068,2	K562	blood:
12	chr16:71156761..71157534-chr4:86089661..86090552,2	MCF-7	breast:
13	chr4:86317452..86319452-chr4:86408462..86411289,2	MCF-7	breast:
14	chr4:86164928..86165741-chr4:86291153..86292328,4	MCF-7	breast:
15	chr4:86234301..86236109-chr4:86239273..86242093,2	K562	blood:
16	chr4:86153952..86155655-chr4:86156797..86158947,2	MCF-7	breast:
17	chr4:86310843..86313430-chr4:86339747..86342570,2	K562	blood:
18	chr4:86068807..86069313-chr4:87816662..87817570,2	K562	blood:
19	chr4:86129889..86132757-chr4:86146969..86148539,2	K562	blood:
20	chr4:86068287..86068959-chr4:86164739..86165523,2	MCF-7	breast:
21	chr4:86100478..86103305-chr4:86104929..86106522,2	K562	blood:
22	chr4:86320129..86322866-chr4:86332900..86334770,2	K562	blood:
23	chr4:86180824..86182598-chr4:86183474..86185368,2	MCF-7	breast:
24	chr4:86129889..86132757-chr4:86146969..86148539,2	K562	blood:
25	chr4:86286749..86288574-chr4:86295386..86298068,2	K562	blood:
26	chr4:86170923..86173404-chr4:86177410..86179415,2	K562	blood:
27	chr4:86100478..86103305-chr4:86104929..86106522,2	K562	blood:
28	chr4:86068869..86069585-chr4:86668543..86669322,2	MCF-7	breast:
29	chr4:86070706..86072618-chr4:86075988..86078281,2	MCF-7	breast:
30	chr4:86181906..86184238-chr4:86188477..86190210,2	MCF-7	breast:
31	chr4:86258169..86261616-chr4:86269942..86273254,3	MCF-7	breast:
32	chr4:86048857..86049411-chr4:86239183..86239916,2	MCF-7	breast:
33	chr4:86258169..86261616-chr4:86269942..86273254,3	MCF-7	breast:
34	chr4:86170923..86173404-chr4:86177410..86179415,2	K562	blood:
35	chr4:86181906..86184238-chr4:86188477..86190210,2	MCF-7	breast:
36	chr4:86180824..86182598-chr4:86183474..86185368,2	MCF-7	breast:
37	chr4:86068287..86068959-chr4:86164739..86165523,2	MCF-7	breast:
38	chr4:86068352..86069122-chr4:86291595..86292351,2	MCF-7	breast:
39	chr4:86068352..86069122-chr4:86291595..86292351,2	MCF-7	breast:
40	chr4:86153952..86155655-chr4:86156797..86158947,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP24-3	chr4:86140868-86140942	ucscGeneNc_uc003hpg_2
2	lnc-ARHGAP24-3	chr4:86144407-86144504	ucscGeneNc_uc003hpg_2
3	lnc-ARHGAP24-3	chr4:86106995-86107304	ucscGeneNc_uc003hpg_2
4	lnc-ARHGAP24-3	chr4:86109902-86110053	ucscGeneNc_uc003hpg_2
5	lnc-ARHGAP24-3	chr4:86146184-86147192	ucscGeneNc_uc003hpg_2
6	lnc-ARHGAP24-3	chr4:86145651-86145745	ucscGeneNc_uc003hpg_2

No data

Variant related genes	Relation type
ENSG00000248725	TF binding region
ENSG00000248725	CpG island
ENSG00000101040	chromatin interactions

Extended variants
information (count: 5066 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5066 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183773234	chr4:86034501-86034502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548752823	chr4:86034537-86034538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189624587	chr4:86034548-86034549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537738471	chr4:86034566-86034567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556380326	chr4:86034571-86034572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553780636	chr4:86035229-86035230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs60956803	chr4:86035231-86035232	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs56094513	chr4:86035240-86035241	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554609715	chr4:86035259-86035260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59049643	chr4:86035276-86035277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576059513	chr4:86035297-86035298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374378696	chr4:86035308-86035309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145093653	chr4:86035324-86035325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146882984	chr4:86035325-86035326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554476539	chr4:86035362-86035363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577108325	chr4:86035366-86035367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74590795	chr4:86035397-86035398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559623792	chr4:86037007-86037008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529982332	chr4:86037022-86037023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576763630	chr4:86037041-86037042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563606552	chr4:86037057-86037058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530377095	chr4:86037063-86037064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114861593	chr4:86037080-86037081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57443529	chr4:86037097-86037098	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs534445247	chr4:86037118-86037119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17009477	chr4:86037130-86037131	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs13101384	chr4:86037150-86037151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368399719	chr4:86037167-86037168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536136539	chr4:86037172-86037173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557331793	chr4:86037195-86037196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575898092	chr4:86037226-86037227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574242961	chr4:86037247-86037248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539814446	chr4:86037269-86037270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558199154	chr4:86037284-86037285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7663977	chr4:86037304-86037305	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191978462	chr4:86037354-86037355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559585528	chr4:86037358-86037359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375814626	chr4:86037359-86037360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542008908	chr4:86037379-86037380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs58339031	chr4:86037396-86037397	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576793015	chr4:86037464-86037465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530847452	chr4:86037525-86037526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149022815	chr4:86037578-86037579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79000654	chr4:86037624-86037625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs80141140	chr4:86037626-86037627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75066855	chr4:86037628-86037629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546328816	chr4:86037665-86037666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143081378	chr4:86037707-86037708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72962210	chr4:86037764-86037765	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138707559	chr4:86037780-86037781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:494 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86034400-86034600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:86035200-86035400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:86037000-86037400	Enhancers	Pancreas	Pancrea
4	chr4:86037400-86038800	Weak transcription	Pancreas	Pancrea
5	chr4:86038800-86039600	Enhancers	Adipose Nuclei	Adipose
6	chr4:86039000-86039200	Enhancers	Pancreas	Pancrea
7	chr4:86043000-86043800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:86043800-86044800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:86044800-86045600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:86045600-86046000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:86045800-86046000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:86045800-86047400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:86045800-86048400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr4:86046000-86046200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:86046000-86046800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr4:86046200-86046600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:86046400-86047800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:86046600-86047000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr4:86046600-86047000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:86046600-86047400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr4:86046600-86047600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:86046600-86049000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:86046600-86049400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:86046800-86047200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:86046800-86047400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr4:86046800-86051000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr4:86047000-86047400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr4:86047000-86049200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:86047200-86047400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:86047200-86048000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:86047200-86048600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr4:86047400-86047600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr4:86047400-86047600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:86047400-86048400	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr4:86047400-86048400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:86047400-86048400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr4:86047600-86048000	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr4:86047600-86049200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:86047600-86049200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr4:86047800-86048200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr4:86047800-86049400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr4:86048000-86049000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:86048000-86049400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr4:86048000-86051400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:86048200-86050000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr4:86048400-86048800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr4:86048400-86049200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr4:86048400-86050200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr4:86048400-86051400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr4:86048600-86049000	Enhancers	Fetal Brain Male	brain

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