Variant report

Variant	nsv524354
Chromosome Location	chr4:85006975-85215142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1224)
CpG islands
(count:550)
Chromatin interactive
region (count:31)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:85201066-85201147	K562	blood:	n/a	n/a
2	ATF1	chr4:85158186-85158535	K562	blood:	n/a	n/a
3	ATF1	chr4:85165754-85165952	K562	blood:	n/a	n/a
4	ATF1	chr4:85178825-85179057	K562	blood:	n/a	n/a
5	ATF1	chr4:85152699-85153034	K562	blood:	n/a	n/a
6	ATF2	chr4:85156731-85157066	GM12878	blood:	n/a	n/a
7	ATF2	chr4:85180433-85180723	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:85158247-85158485	K562	blood:	n/a	n/a
9	BACH1	chr4:85200981-85201146	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:85067531-85067809	GM12878	blood:	n/a	n/a
11	BATF	chr4:85180074-85180335	GM12878	blood:	n/a	chr4:85180194-85180205
12	BATF	chr4:85180048-85180299	GM12878	blood:	n/a	chr4:85180194-85180205
13	BHLHE40	chr4:85165637-85165726	K562	blood:	n/a	n/a
14	BHLHE40	chr4:85158275-85158640	K562	blood:	n/a	n/a
15	BHLHE40	chr4:85152697-85152993	K562	blood:	n/a	n/a
16	BHLHE40	chr4:85067585-85067821	GM12878	blood:	n/a	n/a
17	CBX3	chr4:85181689-85182115	HCT-116	colon:	n/a	n/a
18	CBX3	chr4:85088813-85089099	HCT-116	colon:	n/a	n/a
19	CEBPB	chr4:85017568-85017768	K562	blood:	n/a	chr4:85017666-85017677
20	CEBPB	chr4:85057686-85057780	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:85205456-85205743	IMR90	lung:	n/a	chr4:85205587-85205598 chr4:85205586-85205597
22	CEBPB	chr4:85079993-85080193	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:85205499-85205733	A549	lung:	n/a	chr4:85205587-85205598 chr4:85205586-85205597
24	CEBPB	chr4:85017533-85017825	IMR90	lung:	n/a	chr4:85017666-85017677
25	CEBPB	chr4:85163346-85163549	K562	blood:	n/a	n/a
26	CEBPB	chr4:85119744-85120069	IMR90	lung:	n/a	chr4:85119904-85119915
27	CEBPB	chr4:85199101-85199458	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:85175743-85175944	H1-hESC	embryonic stem cell:	n/a	chr4:85175883-85175894
29	CEBPB	chr4:85014175-85014209	HepG2	liver:	n/a	chr4:85014190-85014201 chr4:85014188-85014201 chr4:85014188-85014199
30	CEBPB	chr4:85199084-85199512	K562	blood:	n/a	n/a
31	CEBPB	chr4:85175724-85176062	K562	blood:	n/a	chr4:85175883-85175894
32	CEBPB	chr4:85135969-85136221	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:85159377-85159684	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr4:85175715-85176027	A549	lung:	n/a	chr4:85175883-85175894
35	CEBPB	chr4:85159385-85159752	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:85199121-85199340	MCF-7	breast:	n/a	n/a
37	CEBPB	chr4:85148336-85148471	HepG2	liver:	n/a	chr4:85148391-85148402
38	CEBPB	chr4:85119769-85120419	A549	lung:	n/a	chr4:85119904-85119915
39	CEBPB	chr4:85163236-85163510	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:85084572-85084750	HepG2	liver:	n/a	chr4:85084721-85084730 chr4:85084719-85084730
41	CEBPB	chr4:85199112-85199489	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:85199051-85199470	A549	lung:	n/a	n/a
43	CEBPB	chr4:85199102-85199389	MCF-7	breast:	n/a	n/a
44	CEBPB	chr4:85017500-85017839	HepG2	liver:	n/a	chr4:85017666-85017677
45	CEBPB	chr4:85148398-85148410	K562	blood:	n/a	n/a
46	CEBPB	chr4:85108449-85108714	H1-hESC	embryonic stem cell:	n/a	chr4:85108566-85108577
47	CEBPB	chr4:85175712-85176074	IMR90	lung:	n/a	chr4:85175883-85175894
48	CEBPB	chr4:85175727-85176070	HepG2	liver:	n/a	chr4:85175883-85175894
49	CEBPB	chr4:85080088-85080249	IMR90	lung:	n/a	n/a
50	CEBPB	chr4:85163228-85163479	A549	lung:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:85020829-85020879	Jurkat	blood:	n/a
2	chr4:85020829-85020879	Jurkat	blood:	n/a
3	chr4:85165491-85165541	PrEC	prostate:	n/a
4	chr4:85048240-85048290	PrEC	prostate:	n/a
5	chr4:85076551-85076601	NHDF-neo	bronchial:	n/a
6	chr4:85165689-85165739	SKMC	muscle:	n/a
7	chr4:85165491-85165541	A549	lung:	n/a
8	chr4:85020829-85020879	PANC-1	pancreas:	n/a
9	chr4:85145324-85145374	MCF10A-Er-Src	breast:	n/a
10	chr4:85076551-85076601	AG04449	skin:	fetal
11	chr4:85076551-85076601	HCF	heart:	n/a
12	chr4:85139232-85139282	PrEC	prostate:	n/a
13	chr4:85139232-85139282	Caco-2	colon:	n/a
14	chr4:85165491-85165541	LNCaP	prostate:	n/a
15	chr4:85165689-85165739	NHDF-neo	bronchial:	n/a
16	chr4:85076551-85076601	PFSK-1	brain:	n/a
17	chr4:85048240-85048290	SAEC	small airway:	n/a
18	chr4:85205711-85205761	AG09319	gingival:	n/a
19	chr4:85165689-85165739	MCF-7	breast:	n/a
20	chr4:85205711-85205761	K562	blood:	n/a
21	chr4:85139232-85139282	GM12878	blood:	n/a
22	chr4:85048240-85048290	PFSK-1	brain:	n/a
23	chr4:85048240-85048290	ECC-1	luminal epithelium:	n/a
24	chr4:85020829-85020879	GM12878	blood:	n/a
25	chr4:85163562-85163612	NHBE	bronchial:	n/a
26	chr4:85163562-85163612	ProgFib	skin:	n/a
27	chr4:85205711-85205761	ProgFib	skin:	n/a
28	chr4:85165689-85165739	Hepatocyte	liver:	n/a
29	chr4:85139232-85139282	HAEpiC	amniotic membrane:	n/a
30	chr4:85205711-85205761	Hepatocyte	liver:	n/a
31	chr4:85165689-85165739	SAEC	small airway:	n/a
32	chr4:85165689-85165739	HCF	heart:	n/a
33	chr4:85020829-85020879	AG04450	lung:	fetal
34	chr4:85165491-85165541	HRPEpiC	eye:	n/a
35	chr4:85163562-85163612	SKMC	muscle:	n/a
36	chr4:85076551-85076601	K562	blood:	n/a
37	chr4:85205711-85205761	RPTEC	kidney:	n/a
38	chr4:85205711-85205761	MCF10A-Er-Src	breast:	n/a
39	chr4:85165491-85165541	HEK293	kidney:	embryo
40	chr4:85145324-85145374	T-47D	breast:	n/a
41	chr4:85139232-85139282	HRCEpiC	kidney:	n/a
42	chr4:85165689-85165739	SK-N-SH	brain:	n/a
43	chr4:85163562-85163612	HL-60	blood:	n/a
44	chr4:85145324-85145374	NB4	blood:	n/a
45	chr4:85020829-85020879	NHBE	bronchial:	n/a
46	chr4:85076551-85076601	PANC-1	pancreas:	n/a
47	chr4:85205711-85205761	BE2_C	brain:	n/a
48	chr4:85076551-85076601	CMK	blood:	n/a
49	chr4:85145324-85145374	HUVEC	blood vessel:	n/a
50	chr4:85163562-85163612	Jurkat	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:85024708..85027047-chr4:85028536..85030200,2	K562	blood:
2	chr4:85072451..85073423-chr4:85180134..85180901,4	MCF-7	breast:
3	chr4:85159698..85160208-chr4:85372408..85372912,2	MCF-7	breast:
4	chr4:85080701..85081585-chr4:85425136..85425979,2	MCF-7	breast:
5	chr4:85200318..85202526-chr4:85203716..85205846,2	MCF-7	breast:
6	chr4:85103034..85104935-chr4:85113026..85114643,2	K562	blood:
7	chr4:85143338..85145421-chr4:85146842..85148891,2	K562	blood:
8	chr4:85072631..85073368-chr4:85450368..85450912,2	MCF-7	breast:
9	chr4:85174053..85178031-chr4:85178404..85182259,4	K562	blood:
10	chr4:85139303..85141304-chr4:85144022..85145808,2	K562	blood:
11	chr4:84827046..84827675-chr4:85088517..85089246,2	MCF-7	breast:
12	chr4:85194924..85197850-chr4:85199277..85201015,2	K562	blood:
13	chr4:85143892..85145421-chr4:85147391..85149801,2	K562	blood:
14	chr4:85198661..85201031-chr4:85203402..85205789,2	K562	blood:
15	chr4:85080575..85081559-chr4:85180120..85181416,6	MCF-7	breast:
16	chr4:85194924..85197850-chr4:85199277..85201015,2	K562	blood:
17	chr4:85072431..85073209-chr4:85424476..85425190,3	MCF-7	breast:
18	chr4:84565617..84566470-chr4:85088713..85089282,2	MCF-7	breast:
19	chr4:85139303..85141304-chr4:85144022..85145808,2	K562	blood:
20	chr4:85174053..85178031-chr4:85178404..85182259,4	K562	blood:
21	chr4:85103034..85104935-chr4:85113026..85114643,2	K562	blood:
22	chr4:85143338..85145421-chr4:85146842..85148891,2	K562	blood:
23	chr4:85024708..85027047-chr4:85028536..85030200,2	K562	blood:
24	chr4:85072451..85073423-chr4:85180134..85180901,4	MCF-7	breast:
25	chr4:85080575..85081559-chr4:85180120..85181416,6	MCF-7	breast:
26	chr4:85071031..85073190-chr4:85079864..85082804,2	MCF-7	breast:
27	chr4:85191697..85192557-chr4:85372441..85373864,5	MCF-7	breast:
28	chr20:52481552..52482195-chr4:85078491..85079377,2	MCF-7	breast:
29	chr4:85071031..85073190-chr4:85079864..85082804,2	MCF-7	breast:
30	chr4:85143892..85145421-chr4:85147391..85149801,2	K562	blood:
31	chr4:84882460..84883415-chr4:85088632..85089152,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKX6-1-3	chr4:85075800-85075907	ucscGeneNc_uc010ikd_1
2	lnc-NKX6-1-2	chr4:85070372-85070441	ENSG00000250546
3	lnc-NKX6-1-2	chr4:85205359-85205480	NONHSAT097229
4	lnc-NKX6-1-2	chr4:85069200-85069283	ENSG00000250546
5	lnc-NKX6-1-2	chr4:85070372-85070409	ENSG00000250546
6	lnc-NKX6-1-2	chr4:85068886-85069283	ENSG00000250546
7	lnc-NKX6-1-2	chr4:85214373-85214565	ENSG00000250546
8	lnc-NKX6-1-2	chr4:85164264-85164369	NONHSAT097229
9	lnc-NKX6-1-2	chr4:85164264-85164369	ENSG00000250546
10	lnc-NKX6-1-2	chr4:85207822-85207980	ENSG00000250546
11	lnc-NKX6-1-2	chr4:85205359-85205479	ENSG00000250546
12	lnc-NKX6-1-3	chr4:85152232-85152296	ucscGeneNc_uc010ikd_1

No data

Variant related genes	Relation type
ENSG00000250546	TF binding region
RNU6-774P	TF binding region
ENSG00000214980	TF binding region
ENSG00000250546	CpG island
RNU6-774P	CpG island
ENSG00000214980	CpG island
ENSG00000250546	chromatin interactions
FAM3C	miRNA target sites
ITGB8	miRNA target sites
VAMP2	miRNA target sites
C18orf19	miRNA target sites
FOXP1	miRNA target sites
F3	miRNA target sites
DYRK2	miRNA target sites
USP25	miRNA target sites

Extended variants
information (count: 3766 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:3766 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551986042	chr4:85007414-85007415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570833605	chr4:85007480-85007481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373423368	chr4:85007522-85007523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs57433897	chr4:85007549-85007550	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs565006913	chr4:85007574-85007575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183523031	chr4:85007588-85007589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6811978	chr4:85007860-85007861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs573373545	chr4:85007868-85007869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184546846	chr4:85007878-85007879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143108619	chr4:85007886-85007887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554717462	chr4:85007904-85007905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541463819	chr4:85007958-85007959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74457222	chr4:85008002-85008003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550196961	chr4:85008004-85008005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533884541	chr4:85008022-85008023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552207797	chr4:85008057-85008058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1921863	chr4:85008082-85008083	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs17008039	chr4:85008186-85008187	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs547070297	chr4:85008219-85008220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79300769	chr4:85008242-85008243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535836216	chr4:85008250-85008251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557420182	chr4:85008264-85008265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202154629	chr4:85008288-85008289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569296732	chr4:85008290-85008291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540105774	chr4:85008340-85008341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558177603	chr4:85008342-85008343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573338515	chr4:85008343-85008344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1921862	chr4:85008360-85008361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553022735	chr4:85008422-85008423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139841252	chr4:85008473-85008474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574226477	chr4:85008480-85008481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541400457	chr4:85008481-85008482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561154243	chr4:85008487-85008488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188096090	chr4:85008501-85008502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530438000	chr4:85008519-85008520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192732933	chr4:85008533-85008534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146279205	chr4:85008560-85008561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201447594	chr4:85008577-85008578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371962508	chr4:85008584-85008585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528281880	chr4:85008595-85008596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546514164	chr4:85008610-85008611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568548031	chr4:85008674-85008675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529379061	chr4:85008689-85008690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551111235	chr4:85008781-85008782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562882061	chr4:85008787-85008788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539844335	chr4:85008797-85008798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558423705	chr4:85008807-85008808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567092045	chr4:85008809-85008810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534387443	chr4:85008875-85008876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376167496	chr4:85008910-85008911	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
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
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85007400-85007600	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr4:85007800-85008800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:85008600-85009000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:85008600-85009200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:85008600-85009200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:85008800-85009200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr4:85008800-85009200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:85008800-85009200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:85008800-85009400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:85008800-85009400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr4:85009000-85009400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:85009000-85009400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:85009000-85009400	Enhancers	Placenta Amnion	Placenta Amnion
14	chr4:85009400-85015000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr4:85010800-85012800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:85011000-85011400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr4:85011200-85013000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr4:85011200-85013000	Enhancers	Fetal Muscle Leg	muscle
19	chr4:85012000-85013400	Enhancers	Fetal Brain Male	brain
20	chr4:85013400-85013800	Weak transcription	Fetal Brain Male	brain
21	chr4:85013800-85014200	Enhancers	Fetal Brain Male	brain
22	chr4:85015000-85015200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
23	chr4:85015200-85020800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr4:85020000-85020800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:85020400-85021800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:85020600-85021200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:85020600-85021200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:85020600-85021600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:85020600-85021800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr4:85020800-85021000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:85020800-85021200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr4:85020800-85021200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:85020800-85021600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr4:85020800-85021600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:85020800-85021800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr4:85020800-85021800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:85021000-85021400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr4:85021000-85021400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:85021200-85021600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr4:85021200-85022000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:85021400-85021800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr4:85021600-85021800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr4:85025800-85026400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr4:85026400-85030200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr4:85030200-85032800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr4:85030400-85031600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr4:85031200-85031400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:85031200-85031600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr4:85031400-85031600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:85047000-85047600	Enhancers	HUES64 Cell Line	embryonic stem cell

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