Variant report

Variant	nsv521867
Chromosome Location	chr4:8608066-8641696
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	BCL3	chr4:8610576-8611046	GM12878	blood:	n/a	n/a
2	BCL3	chr4:8612532-8612922	GM12878	blood:	n/a	n/a
3	BCL3	chr4:8610662-8611065	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:8610202-8610572	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:8609354-8609763	K562	blood:	n/a	chr4:8609588-8609601
6	BHLHE40	chr4:8609534-8609694	A549	lung:	n/a	chr4:8609588-8609601
7	BHLHE40	chr4:8609413-8609700	HepG2	liver:	n/a	chr4:8609588-8609601
8	BHLHE40	chr4:8609432-8609738	GM12878	blood:	n/a	chr4:8609588-8609601
9	BRCA1	chr4:8609386-8609627	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr4:8609454-8609550	HepG2	liver:	n/a	n/a
11	CBX3	chr4:8637918-8638194	K562	blood:	n/a	n/a
12	CBX3	chr4:8637870-8638277	K562	blood:	n/a	n/a
13	CBX3	chr4:8632192-8632581	K562	blood:	n/a	n/a
14	CBX3	chr4:8626547-8627016	K562	blood:	n/a	n/a
15	CCNT2	chr4:8609385-8609607	K562	blood:	n/a	chr4:8609415-8609424
16	CHD2	chr4:8609527-8609681	K562	blood:	n/a	n/a
17	CHD2	chr4:8609419-8609693	H1-hESC	embryonic stem cell:	n/a	chr4:8609458-8609468
18	CHD2	chr4:8609474-8609658	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr4:8609281-8609288	MCF-7	breast:	n/a	n/a
20	CTCF	chr4:8609480-8609630	HepG2	liver:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
21	CTCF	chr4:8609378-8609630	Lung_OC	lung:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
22	CTCF	chr4:8609400-8609550	HEEpiC	esophagus:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
23	CTCF	chr4:8609440-8609590	NHDF-neo	bronchial:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
24	CTCF	chr4:8609130-8609700	GM12891	blood:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
25	CTCF	chr4:8609423-8609640	HepG2	liver:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
26	CTCF	chr4:8609184-8609699	GM19238	blood:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
27	CTCF	chr4:8609345-8609678	A549	lung:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
28	CTCF	chr4:8609900-8610050	GM12872	blood:	n/a	chr4:8609920-8609929
29	CTCF	chr4:8637959-8638155	A549	lung:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
30	CTCF	chr4:8609440-8609590	HPF	lung:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
31	CTCF	chr4:8632169-8632674	A549	lung:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
32	CTCF	chr4:8626340-8627148	K562	blood:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
33	CTCF	chr4:8632203-8632617	A549	lung:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
34	CTCF	chr4:8624234-8624278	LNCaP	prostate:	n/a	n/a
35	CTCF	chr4:8609460-8609610	AG04449	skin:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
36	CTCF	chr4:8637981-8638196	GM10248	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
37	CTCF	chr4:8609460-8609610	GM12866	blood:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
38	CTCF	chr4:8609198-8609697	Gliobla	brain:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
39	CTCF	chr4:8609460-8609610	AG09309	skin:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
40	CTCF	chr4:8609460-8609610	AG09319	gingival:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
41	CTCF	chr4:8609374-8609620	SK-N-SH_RA	brain:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
42	CTCF	chr4:8609376-8609682	GM12878	blood:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
43	CTCF	chr4:8609301-8609740	GM12878	blood:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
44	CTCF	chr4:8632310-8632572	LNCaP	prostate:	n/a	chr4:8632423-8632441 chr4:8632429-8632438 chr4:8632425-8632438 chr4:8632424-8632440 chr4:8632426-8632436 chr4:8632425-8632438
45	CTCF	chr4:8609440-8609590	GM12867	blood:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
46	CTCF	chr4:8633760-8633910	K562	blood:	n/a	n/a
47	CTCF	chr4:8626673-8626869	A549	lung:	n/a	chr4:8626789-8626802 chr4:8626788-8626804 chr4:8626789-8626802 chr4:8626793-8626802 chr4:8626790-8626800 chr4:8626787-8626805
48	CTCF	chr4:8609440-8609590	AoAF	blood vessel:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
49	CTCF	chr4:8609360-8609679	H1-hESC	embryonic stem cell:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
50	CTCF	chr4:8608780-8608930	WI-38	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8628157-8628207	K562	blood:	n/a
2	chr4:8608486-8608536	AG10803	skin:	n/a
3	chr4:8615996-8616046	BE2_C	brain:	n/a
4	chr4:8608235-8608285	HRPEpiC	eye:	n/a
5	chr4:8628157-8628207	Jurkat	blood:	n/a
6	chr4:8628157-8628207	AG09309	skin:	n/a
7	chr4:8616045-8616095	AG09319	gingival:	n/a
8	chr4:8621226-8621276	NHBE	bronchial:	n/a
9	chr4:8616045-8616095	T-47D	breast:	n/a
10	chr4:8633794-8633844	HAEpiC	amniotic membrane:	n/a
11	chr4:8609401-8609451	HRPEpiC	eye:	n/a
12	chr4:8609706-8609756	HL-60	blood:	n/a
13	chr4:8608486-8608536	Hela-S3	cervix:	n/a
14	chr4:8640896-8640946	HCPEpiC	choroid plexus:	n/a
15	chr4:8623002-8623052	GM12878	blood:	n/a
16	chr4:8617839-8617889	ovcar-3	ovarian:	n/a
17	chr4:8640896-8640946	AG09319	gingival:	n/a
18	chr4:8616045-8616095	AG09309	skin:	n/a
19	chr4:8617910-8617960	AG04450	lung:	fetal
20	chr4:8621361-8621411	Jurkat	blood:	n/a
21	chr4:8623002-8623052	HUVEC	blood vessel:	n/a
22	chr4:8608361-8608411	CMK	blood:	n/a
23	chr4:8617738-8617788	HRCEpiC	kidney:	n/a
24	chr4:8608486-8608536	PANC-1	pancreas:	n/a
25	chr4:8640896-8640946	HCT-116	colon:	n/a
26	chr4:8619939-8619989	ECC-1	luminal epithelium:	n/a
27	chr4:8609594-8609644	GM19239	blood:	n/a
28	chr4:8609401-8609451	NHBE	bronchial:	n/a
29	chr4:8608235-8608285	PrEC	prostate:	n/a
30	chr4:8617910-8617960	ECC-1	luminal epithelium:	n/a
31	chr4:8640896-8640946	GM12891	blood:	n/a
32	chr4:8623002-8623052	T-47D	breast:	n/a
33	chr4:8617910-8617960	PrEC	prostate:	n/a
34	chr4:8617839-8617889	HL-60	blood:	n/a
35	chr4:8608235-8608285	HRE	kidney:	n/a
36	chr4:8609401-8609451	SK-N-MC	brain:	n/a
37	chr4:8609594-8609644	NHDF-neo	bronchial:	n/a
38	chr4:8639337-8639387	GM19239	blood:	n/a
39	chr4:8619939-8619989	AG09309	skin:	n/a
40	chr4:8608361-8608411	AG09309	skin:	n/a
41	chr4:8621361-8621411	NHBE	bronchial:	n/a
42	chr4:8621226-8621276	IMR90	lung:	fetal
43	chr4:8623002-8623052	RPTEC	kidney:	n/a
44	chr4:8615996-8616046	GM12878	blood:	n/a
45	chr4:8621226-8621276	AG10803	skin:	n/a
46	chr4:8609706-8609756	SAEC	small airway:	n/a
47	chr4:8620162-8620212	A549	lung:	n/a
48	chr4:8621266-8621316	HNPCEpiC	eye:	n/a
49	chr4:8616045-8616095	GM12891	blood:	n/a
50	chr4:8621266-8621316	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:8594040..8595789-chr4:8608077..8610422,2	MCF-7	breast:
2	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
3	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
4	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
5	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
6	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
7	chr4:8609002..8610016-chr4:8919155..8920078,6	MCF-7	breast:
8	chr4:8609226..8610032-chr4:8887698..8888205,2	MCF-7	breast:
9	chr4:8472717..8474725-chr4:8621251..8624026,2	K562	blood:
10	chr4:8604553..8606540-chr4:8607081..8609786,2	MCF-7	breast:
11	chr4:8617932..8619527-chr4:8918338..8920672,2	MCF-7	breast:
12	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:

Variant related genes	Relation type
CPZ	TF binding region
CPZ	CpG island
ENSG00000109625	chromatin interactions

Extended variants
information (count: 1560 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1560 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2302581	chr4:8608066-8608067	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560480016	chr4:8608077-8608078	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572573966	chr4:8608087-8608088	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs543115285	chr4:8608098-8608099	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368597276	chr4:8608100-8608101	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529057031	chr4:8608108-8608109	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs544542126	chr4:8608163-8608164	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs376214208	chr4:8608175-8608176	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562632034	chr4:8608210-8608211	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs41266533	chr4:8608265-8608266	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs138293094	chr4:8608285-8608286	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113477164	chr4:8608296-8608297	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566106490	chr4:8608300-8608301	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs527403447	chr4:8608323-8608324	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374936459	chr4:8608332-8608333	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs565995491	chr4:8608361-8608362	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549973147	chr4:8608389-8608390	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538050095	chr4:8608396-8608397	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375073957	chr4:8608434-8608435	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs556854523	chr4:8608438-8608439	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201336324	chr4:8608444-8608445	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373523491	chr4:8608461-8608462	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111338063	chr4:8608469-8608470	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs199906050	chr4:8608502-8608503	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370892504	chr4:8608505-8608506	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs146935182	chr4:8608506-8608507	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201140095	chr4:8608507-8608508	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200412441	chr4:8608511-8608512	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538634471	chr4:8608525-8608526	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs374225290	chr4:8608526-8608527	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs137864072	chr4:8608538-8608539	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377478120	chr4:8608543-8608544	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371225755	chr4:8608544-8608545	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374338787	chr4:8608547-8608548	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149008174	chr4:8608556-8608557	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183698544	chr4:8608558-8608559	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143844162	chr4:8608571-8608572	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200376379	chr4:8608572-8608573	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368933993	chr4:8608573-8608574	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201029859	chr4:8608575-8608576	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200282318	chr4:8608577-8608578	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs559753840	chr4:8608578-8608579	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148162472	chr4:8608582-8608583	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs141960829	chr4:8608585-8608586	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs199572540	chr4:8608595-8608596	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376030472	chr4:8608598-8608599	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149186746	chr4:8608618-8608619	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs531394795	chr4:8608619-8608620	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs150237935	chr4:8608622-8608623	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs74940399	chr4:8608627-8608628	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8573400-8609400	Weak transcription	Right Atrium	heart
2	chr4:8596000-8622800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:8596000-8623200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:8596200-8609000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr4:8597600-8618400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:8598800-8609000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:8599600-8616000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:8599800-8609000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:8600800-8608400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
10	chr4:8601200-8611400	Weak transcription	Spleen	Spleen
11	chr4:8601400-8609000	Strong transcription	H1 Cell Line	embryonic stem cell
12	chr4:8601400-8616000	Weak transcription	HSMMtube	muscle
13	chr4:8601600-8609600	Strong transcription	Ovary	ovary
14	chr4:8601600-8620200	Weak transcription	NHDF-Ad	bronchial
15	chr4:8601800-8617000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:8601800-8622000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr4:8602400-8608600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:8603200-8609200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:8603200-8615400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr4:8604000-8608200	Strong transcription	Placenta	Placenta
21	chr4:8604800-8608600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr4:8605800-8612000	Weak transcription	Gastric	stomach
23	chr4:8606000-8609000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:8606800-8615400	Weak transcription	Osteobl	bone
25	chr4:8607800-8616000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr4:8608000-8610200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:8608000-8613000	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr4:8608200-8610400	Genic enhancers	Placenta	Placenta
29	chr4:8608400-8614200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr4:8608600-8609000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr4:8609000-8609200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr4:8609000-8609200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
33	chr4:8609000-8609200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:8609000-8609400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr4:8609000-8609600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr4:8609000-8610200	Genic enhancers	H1 Cell Line	embryonic stem cell
37	chr4:8609200-8609400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
38	chr4:8609200-8609400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
39	chr4:8609200-8609400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:8609200-8609600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr4:8609200-8609600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr4:8609200-8609800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr4:8609200-8609800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr4:8609200-8609800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:8609200-8609800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:8609200-8609800	Enhancers	Adipose Nuclei	Adipose
47	chr4:8609200-8609800	Active TSS	Brain Germinal Matrix	brain
48	chr4:8609200-8609800	Bivalent Enhancer	Fetal Brain Male	brain
49	chr4:8609200-8609800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr4:8609200-8609800	Bivalent Enhancer	Fetal Muscle Leg	muscle

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