Variant report

Variant	nsv593464
Chromosome Location	chr4:3683269-3714659
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	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr4:3714099-3714481	GM12878	blood:	n/a	n/a
3	BCL3	chr4:3714152-3714450	GM12878	blood:	n/a	n/a
4	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
6	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
7	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
8	CEBPB	chr4:3710716-3710755	K562	blood:	n/a	n/a
9	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
10	CTCF	chr4:3703300-3703450	HepG2	liver:	n/a	chr4:3703375-3703384
11	CTCF	chr4:3703280-3703430	NB4	blood:	n/a	chr4:3703375-3703384
12	CTCF	chr4:3703300-3703450	A549	lung:	n/a	chr4:3703375-3703384
13	CTCF	chr4:3698147-3698188	MCF-7	breast:	n/a	n/a
14	CTCF	chr4:3687710-3687759	GM12892	blood:	n/a	n/a
15	CTCF	chr4:3703280-3703430	K562	blood:	n/a	chr4:3703375-3703384
16	CTCF	chr4:3698092-3698194	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:3703320-3703470	HEK293	kidney:	n/a	chr4:3703375-3703384
18	CTCF	chr4:3703260-3703410	HepG2	liver:	n/a	chr4:3703375-3703384
19	CTCF	chr4:3703280-3703430	HRPEpiC	eye:	n/a	chr4:3703375-3703384
20	CTCF	chr4:3709620-3709770	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr4:3698143-3698164	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:3703327-3703392	MCF-7	breast:	n/a	chr4:3703375-3703384
23	CTCF	chr4:3703301-3703427	MCF-7	breast:	n/a	chr4:3703375-3703384
24	CTCF	chr4:3703301-3703460	H1-hESC	embryonic stem cell:	n/a	chr4:3703375-3703384
25	CTCF	chr4:3703240-3703390	SK-N-SH_RA	brain:	n/a	chr4:3703375-3703384
26	CTCF	chr4:3703280-3703430	MCF-7	breast:	n/a	chr4:3703375-3703384
27	CTCF	chr4:3703335-3703417	MCF-7	breast:	n/a	chr4:3703375-3703384
28	CTCF	chr4:3703200-3703350	Caco-2	colon:	n/a	n/a
29	CTCF	chr4:3703260-3703410	WERI-Rb-1	eye:	n/a	chr4:3703375-3703384
30	CTCF	chr4:3703280-3703430	AG04449	skin:	n/a	chr4:3703375-3703384
31	CTCF	chr4:3703350-3703499	K562	blood:	n/a	chr4:3703375-3703384
32	CTCF	chr4:3703345-3703409	HepG2	liver:	n/a	chr4:3703375-3703384
33	CTCF	chr4:3703220-3703370	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr4:3703324-3703414	MCF-7	breast:	n/a	chr4:3703375-3703384
35	CTCF	chr4:3709580-3709730	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr4:3707720-3707870	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr4:3703257-3703425	HepG2	liver:	n/a	chr4:3703375-3703384
38	CTCFL	chr4:3703303-3703408	K562	blood:	n/a	n/a
39	E2F4	chr4:3696531-3697077	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr4:3698537-3699091	MCF10A-Er-Src	breast:	n/a	n/a
41	EBF1	chr4:3709948-3710330	GM12878	blood:	n/a	chr4:3710043-3710053 chr4:3710044-3710053 chr4:3710042-3710055 chr4:3710043-3710054
42	EBF1	chr4:3709926-3710350	GM12878	blood:	n/a	chr4:3710043-3710053 chr4:3710044-3710053 chr4:3710042-3710055 chr4:3710043-3710054
43	EGR1	chr4:3709759-3710106	K562	blood:	n/a	chr4:3709922-3709937 chr4:3709924-3709934 chr4:3709923-3709936 chr4:3709922-3709936 chr4:3709923-3709936 chr4:3709925-3709934 chr4:3709924-3709935 chr4:3709923-3709936 chr4:3709924-3709934 chr4:3709923-3709936 chr4:3709924-3709935 chr4:3709918-3709940 chr4:3709924-3709933
44	EGR1	chr4:3709805-3710059	K562	blood:	n/a	chr4:3709922-3709937 chr4:3709924-3709934 chr4:3709923-3709936 chr4:3709922-3709936 chr4:3709923-3709936 chr4:3709925-3709934 chr4:3709924-3709935 chr4:3709923-3709936 chr4:3709924-3709934 chr4:3709923-3709936 chr4:3709924-3709935 chr4:3709918-3709940 chr4:3709924-3709933
45	EGR1	chr4:3706726-3707022	K562	blood:	n/a	chr4:3706899-3706912 chr4:3706900-3706911 chr4:3706902-3706911 chr4:3706899-3706912 chr4:3706900-3706911 chr4:3706899-3706913 chr4:3706901-3706911 chr4:3706901-3706910 chr4:3706899-3706912 chr4:3706898-3706913 chr4:3706901-3706911
46	EGR1	chr4:3706787-3707002	K562	blood:	n/a	chr4:3706899-3706912 chr4:3706900-3706911 chr4:3706902-3706911 chr4:3706899-3706912 chr4:3706900-3706911 chr4:3706899-3706913 chr4:3706901-3706911 chr4:3706901-3706910 chr4:3706899-3706912 chr4:3706898-3706913 chr4:3706901-3706911
47	EGR1	chr4:3709701-3710193	ECC-1	luminal epithelium:	n/a	chr4:3709922-3709937 chr4:3709924-3709934 chr4:3709923-3709936 chr4:3710181-3710190 chr4:3709922-3709936 chr4:3709923-3709936 chr4:3709925-3709934 chr4:3709924-3709935 chr4:3709923-3709936 chr4:3709924-3709934 chr4:3709923-3709936 chr4:3709924-3709935 chr4:3709918-3709940 chr4:3709924-3709933
48	EGR1	chr4:3709720-3710171	ECC-1	luminal epithelium:	n/a	chr4:3709922-3709937 chr4:3709924-3709934 chr4:3709923-3709936 chr4:3709922-3709936 chr4:3709923-3709936 chr4:3709925-3709934 chr4:3709924-3709935 chr4:3709923-3709936 chr4:3709924-3709934 chr4:3709923-3709936 chr4:3709924-3709935 chr4:3709918-3709940 chr4:3709924-3709933
49	EP300	chr4:3708272-3708777	ECC-1	luminal epithelium:	n/a	chr4:3708602-3708616 chr4:3708600-3708614
50	EP300	chr4:3688571-3688905	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3692574-3692624	HAEpiC	amniotic membrane:	n/a
2	chr4:3685309-3685359	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:3692142-3692192	GM12891	blood:	n/a
4	chr4:3691238-3691288	HEEpiC	esophagus:	n/a
5	chr4:3692574-3692624	HAEpiC	amniotic membrane:	n/a
6	chr4:3685309-3685359	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:3692142-3692192	GM12891	blood:	n/a
8	chr4:3691238-3691288	HEEpiC	esophagus:	n/a
9	chr4:3704880-3704930	HRCEpiC	kidney:	n/a
10	chr4:3685577-3685627	PFSK-1	brain:	n/a
11	chr4:3692712-3692762	HEEpiC	esophagus:	n/a
12	chr4:3691397-3691447	GM12892	blood:	n/a
13	chr4:3691908-3691958	HCT-116	colon:	n/a
14	chr4:3692142-3692192	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:3692375-3692425	PFSK-1	brain:	n/a
16	chr4:3691297-3691347	HCF	heart:	n/a
17	chr4:3685875-3685925	HRPEpiC	eye:	n/a
18	chr4:3685438-3685488	Hela-S3	cervix:	n/a
19	chr4:3685309-3685359	Caco-2	colon:	n/a
20	chr4:3691297-3691347	HEEpiC	esophagus:	n/a
21	chr4:3685577-3685627	NHDF-neo	bronchial:	n/a
22	chr4:3713224-3713274	BE2_C	brain:	n/a
23	chr4:3684756-3684806	Hepatocyte	liver:	n/a
24	chr4:3713287-3713337	Hepatocyte	liver:	n/a
25	chr4:3705147-3705197	U87	brain:	n/a
26	chr4:3683268-3683318	HNPCEpiC	eye:	n/a
27	chr4:3691297-3691347	SAEC	small airway:	n/a
28	chr4:3689478-3689528	BE2_C	brain:	n/a
29	chr4:3685875-3685925	AG10803	skin:	n/a
30	chr4:3684756-3684806	U87	brain:	n/a
31	chr4:3685695-3685745	HIPEpiC	eye:	n/a
32	chr4:3704852-3704902	ovcar-3	ovarian:	n/a
33	chr4:3691238-3691288	GM06990	blood:	n/a
34	chr4:3704880-3704930	SK-N-SH	brain:	n/a
35	chr4:3690945-3690995	RPTEC	kidney:	n/a
36	chr4:3705147-3705197	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:3692142-3692192	HL-60	blood:	n/a
38	chr4:3691824-3691874	Hepatocyte	liver:	n/a
39	chr4:3691908-3691958	BJ	skin:	n/a
40	chr4:3713224-3713274	HMEC	breast:	n/a
41	chr4:3704880-3704930	AG04449	skin:	fetal
42	chr4:3691033-3691083	NB4	blood:	n/a
43	chr4:3691824-3691874	NHDF-neo	bronchial:	n/a
44	chr4:3690828-3690878	HNPCEpiC	eye:	n/a
45	chr4:3704852-3704902	GM12892	blood:	n/a
46	chr4:3704880-3704930	BE2_C	brain:	n/a
47	chr4:3691033-3691083	PrEC	prostate:	n/a
48	chr4:3685438-3685488	T-47D	breast:	n/a
49	chr4:3691908-3691958	CMK	blood:	n/a
50	chr4:3713287-3713337	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
2	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
3	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
4	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
5	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
6	chr4:3702976..3705970-chr4:3735549..3737209,2	K562	blood:
7	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
8	chr4:3679034..3681438-chr4:3689559..3691418,2	K562	blood:
9	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
10	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
11	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
12	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
13	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
14	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
15	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
16	chr14:52308290..52309229-chr4:3693785..3694520,2	MCF-7	breast:
17	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
18	chr4:3688266..3689130-chr4:3828986..3829489,2	MCF-7	breast:
19	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
20	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:

Variant related genes	Relation type
ENSG00000250632	TF binding region
ENSG00000250632	CpG island
ENSG00000250632	chromatin interactions

Extended variants
information (count: 1458 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2880892	chr4:3683269-3683270	Weak transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573333680	chr4:3683275-3683276	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs145078828	chr4:3683279-3683280	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs147591099	chr4:3683291-3683292	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs148655186	chr4:3683292-3683293	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs562258302	chr4:3683300-3683301	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs528038576	chr4:3683330-3683331	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs191866913	chr4:3683399-3683400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111724705	chr4:3683415-3683416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183310325	chr4:3683427-3683428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369939852	chr4:3683432-3683433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533186629	chr4:3683475-3683476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550119374	chr4:3683518-3683519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577967203	chr4:3683534-3683535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142177572	chr4:3683551-3683552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199834746	chr4:3683560-3683561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188315446	chr4:3683565-3683566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563240577	chr4:3683586-3683587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs578082228	chr4:3683606-3683607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554382142	chr4:3683608-3683609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10937906	chr4:3683617-3683618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs376259137	chr4:3683622-3683623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs151202638	chr4:3683648-3683649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553799644	chr4:3683658-3683659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192656241	chr4:3683659-3683660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183724367	chr4:3683661-3683662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540067078	chr4:3683677-3683678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576245537	chr4:3683680-3683681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541943991	chr4:3683697-3683698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186636927	chr4:3683716-3683717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192658430	chr4:3683734-3683735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566564587	chr4:3683763-3683764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549500960	chr4:3683764-3683765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367948180	chr4:3683783-3683784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541053186	chr4:3683789-3683790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564646332	chr4:3683790-3683791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4401513	chr4:3683791-3683792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4587016	chr4:3683796-3683797	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs28610211	chr4:3683819-3683820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549052709	chr4:3683822-3683823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529051512	chr4:3683861-3683862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10937907	chr4:3683869-3683870	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs547524554	chr4:3683915-3683916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372351031	chr4:3683918-3683919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375985033	chr4:3683921-3683922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562758973	chr4:3683930-3683931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539710587	chr4:3683939-3683940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184726563	chr4:3683942-3683943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190275447	chr4:3683943-3683944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535576693	chr4:3683968-3683969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	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
Urothelial carcinoma	21177765	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
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3669400-3693400	Weak transcription	Right Atrium	heart
2	chr4:3679400-3685400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:3682000-3685200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:3683400-3683600	Enhancers	Primary hematopoietic stem cells	blood
5	chr4:3685200-3686200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:3685400-3685600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:3685600-3686200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:3686200-3689400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:3689400-3690000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:3689800-3690200	Enhancers	Fetal Muscle Leg	muscle
11	chr4:3690000-3690200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr4:3690000-3690200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:3690200-3691000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:3691000-3692000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:3692000-3692600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:3692600-3693400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:3693400-3693600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:3699800-3710800	Weak transcription	Right Atrium	heart
19	chr4:3700200-3700600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
20	chr4:3700800-3706000	Weak transcription	Aorta	Aorta
21	chr4:3701200-3701400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr4:3701200-3701400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:3701200-3701800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:3701400-3702600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:3701600-3701800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:3701800-3702000	Enhancers	HSMM	muscle
27	chr4:3701800-3702600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:3701800-3704800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:3702000-3703200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:3702400-3703400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr4:3702400-3703600	Enhancers	Brain Germinal Matrix	brain
32	chr4:3702400-3704800	Enhancers	Fetal Brain Male	brain
33	chr4:3702600-3702800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:3702600-3706200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:3702800-3704000	Bivalent Enhancer	Fetal Muscle Leg	muscle
36	chr4:3702800-3705200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:3702800-3705600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr4:3703200-3705000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:3703200-3706000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:3703400-3705800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:3703600-3705200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:3703800-3704000	Enhancers	H1 Cell Line	embryonic stem cell
43	chr4:3703800-3705600	Bivalent Enhancer	Fetal Stomach	stomach
44	chr4:3704000-3704600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr4:3704400-3705400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
46	chr4:3704600-3706600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:3704600-3707000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
48	chr4:3704800-3705000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr4:3704800-3705000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
50	chr4:3704800-3705000	Bivalent Enhancer	Fetal Lung	lung

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