Variant report

Variant	nsv593462
Chromosome Location	chr4:3669171-3719380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:2748)
Chromatin interactive
region (count:30)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3673560-3674036	HepG2	liver:	n/a	n/a
2	ATF2	chr4:3677008-3677424	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:3677029-3677356	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr4:3714099-3714481	GM12878	blood:	n/a	n/a
7	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
8	BCL3	chr4:3714152-3714450	GM12878	blood:	n/a	n/a
9	BCL3	chr4:3715793-3716328	GM12878	blood:	n/a	chr4:3715840-3715849
10	BCL3	chr4:3715787-3716400	GM12878	blood:	n/a	chr4:3715840-3715849
11	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
12	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
13	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
14	CEBPB	chr4:3710716-3710755	K562	blood:	n/a	n/a
15	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
17	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
18	CHD2	chr4:3677157-3677385	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr4:3676953-3677446	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr4:3677024-3677462	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr4:3703324-3703414	MCF-7	breast:	n/a	chr4:3703375-3703384
22	CTCF	chr4:3679316-3679632	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr4:3703345-3703409	HepG2	liver:	n/a	chr4:3703375-3703384
24	CTCF	chr4:3707720-3707870	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr4:3677098-3677329	H1-hESC	embryonic stem cell:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
26	CTCF	chr4:3679420-3679570	BE2_C	brain:	n/a	n/a
27	CTCF	chr4:3679460-3679610	GM12873	blood:	n/a	n/a
28	CTCF	chr4:3679460-3679610	HCT-116	colon:	n/a	n/a
29	CTCF	chr4:3670560-3670710	HCT-116	colon:	n/a	n/a
30	CTCF	chr4:3703280-3703430	K562	blood:	n/a	chr4:3703375-3703384
31	CTCF	chr4:3677185-3677254	MCF-7	breast:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
32	CTCF	chr4:3670574-3670771	HepG2	liver:	n/a	n/a
33	CTCF	chr4:3716502-3716563	GM12891	blood:	n/a	n/a
34	CTCF	chr4:3677018-3677343	K562	blood:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
35	CTCF	chr4:3679478-3679584	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:3682194-3682267	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr4:3680104-3680138	GM10266	blood:	n/a	n/a
38	CTCF	chr4:3677140-3677290	NB4	blood:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
39	CTCF	chr4:3703280-3703430	AG04449	skin:	n/a	chr4:3703375-3703384
40	CTCF	chr4:3670582-3670804	H1-hESC	embryonic stem cell:	n/a	chr4:3670773-3670782
41	CTCF	chr4:3717919-3717984	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr4:3677009-3677377	H1-hESC	embryonic stem cell:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
43	CTCF	chr4:3703335-3703417	MCF-7	breast:	n/a	chr4:3703375-3703384
44	CTCF	chr4:3677190-3677250	ProgFib	skin:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
45	CTCF	chr4:3703200-3703350	Caco-2	colon:	n/a	n/a
46	CTCF	chr4:3703220-3703370	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr4:3679460-3679610	HepG2	liver:	n/a	n/a
48	CTCF	chr4:3670495-3670905	H1-hESC	embryonic stem cell:	n/a	chr4:3670773-3670782
49	CTCF	chr4:3679505-3679566	Gliobla	brain:	n/a	n/a
50	CTCF	chr4:3677140-3677290	GM12864	blood:	n/a	chr4:3677196-3677209 chr4:3677194-3677212

(count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3684756-3684806	NT2-D1	testis:	n/a
2	chr4:3691824-3691874	HCPEpiC	choroid plexus:	n/a
3	chr4:3692712-3692762	U87	brain:	n/a
4	chr4:3684756-3684806	NT2-D1	testis:	n/a
5	chr4:3691824-3691874	HCPEpiC	choroid plexus:	n/a
6	chr4:3692712-3692762	U87	brain:	n/a
7	chr4:3692142-3692192	ProgFib	skin:	n/a
8	chr4:3684756-3684806	HRE	kidney:	n/a
9	chr4:3685309-3685359	ProgFib	skin:	n/a
10	chr4:3680721-3680771	HL-60	blood:	n/a
11	chr4:3704852-3704902	SK-N-SH	brain:	n/a
12	chr4:3671067-3671117	A549	lung:	n/a
13	chr4:3671380-3671430	HL-60	blood:	n/a
14	chr4:3704880-3704930	IMR90	lung:	fetal
15	chr4:3671380-3671430	CMK	blood:	n/a
16	chr4:3680970-3681020	H1-hESC	embryonic stem cell:	embryo
17	chr4:3671697-3671747	AG04450	lung:	fetal
18	chr4:3685309-3685359	GM19239	blood:	n/a
19	chr4:3692574-3692624	SAEC	small airway:	n/a
20	chr4:3671503-3671553	HL-60	blood:	n/a
21	chr4:3671380-3671430	AoSMC	blood vessel:	n/a
22	chr4:3685577-3685627	HUVEC	blood vessel:	n/a
23	chr4:3704880-3704930	HCPEpiC	choroid plexus:	n/a
24	chr4:3704880-3704930	ovcar-3	ovarian:	n/a
25	chr4:3691908-3691958	RPTEC	kidney:	n/a
26	chr4:3671380-3671430	GM19239	blood:	n/a
27	chr4:3690945-3690995	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:3682627-3682677	HAEpiC	amniotic membrane:	n/a
29	chr4:3692142-3692192	HL-60	blood:	n/a
30	chr4:3691824-3691874	HAEpiC	amniotic membrane:	n/a
31	chr4:3713209-3713259	HAEpiC	amniotic membrane:	n/a
32	chr4:3680721-3680771	HNPCEpiC	eye:	n/a
33	chr4:3681759-3681809	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:3691238-3691288	MCF10A-Er-Src	breast:	n/a
35	chr4:3671503-3671553	Hepatocyte	liver:	n/a
36	chr4:3704880-3704930	HEEpiC	esophagus:	n/a
37	chr4:3691908-3691958	U87	brain:	n/a
38	chr4:3692375-3692425	GM12878	blood:	n/a
39	chr4:3675363-3675413	RPTEC	kidney:	n/a
40	chr4:3689478-3689528	IMR90	lung:	fetal
41	chr4:3690945-3690995	Caco-2	colon:	n/a
42	chr4:3691238-3691288	U87	brain:	n/a
43	chr4:3680970-3681020	GM12892	blood:	n/a
44	chr4:3704880-3704930	ECC-1	luminal epithelium:	n/a
45	chr4:3677497-3677547	HRCEpiC	kidney:	n/a
46	chr4:3675120-3675170	SAEC	small airway:	n/a
47	chr4:3677497-3677547	RPTEC	kidney:	n/a
48	chr4:3691908-3691958	MCF-7	breast:	n/a
49	chr4:3685357-3685407	HCM	heart:	n/a
50	chr4:3691297-3691347	CMK	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
2	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
3	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
4	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
5	chr4:3715270..3718190-chr4:3721526..3723393,2	K562	blood:
6	chr4:3717339..3719373-chr4:3721279..3722918,2	MCF-7	breast:
7	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
8	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
9	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
10	chr14:52308290..52309229-chr4:3693785..3694520,2	MCF-7	breast:
11	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
12	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
13	chr4:3679034..3681438-chr4:3689559..3691418,2	K562	blood:
14	chr4:3717857..3720056-chr4:3723644..3725873,2	MCF-7	breast:
15	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
16	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
17	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
18	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
19	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
20	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
21	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
22	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
23	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
24	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
25	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
26	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
27	chr4:3688266..3689130-chr4:3828986..3829489,2	MCF-7	breast:
28	chr4:3702976..3705970-chr4:3735549..3737209,2	K562	blood:
29	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
30	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRPAP1-2	chr4:3675320-3675588	ENSG00000250632
2	lnc-LRPAP1-2	chr4:3678330-3678408	XLOC_003861
3	lnc-LRPAP1-2	chr4:3675321-3675588	XLOC_003861
4	lnc-LRPAP1-2	chr4:3678330-3678408	ENSG00000250632
5	lnc-LRPAP1-2	chr4:3678898-3679582	ENSG00000250632
6	lnc-LRPAP1-2	chr4:3678898-3679582	XLOC_003861

No data

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

Extended variants
information (count: 2516 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2516 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58513064	chr4:3669171-3669172	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs190285678	chr4:3669216-3669217	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs554746013	chr4:3669220-3669221	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs574688864	chr4:3669233-3669234	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs374774446	chr4:3669282-3669283	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs566759755	chr4:3669283-3669284	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs114215057	chr4:3669323-3669324	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs560605266	chr4:3669340-3669341	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs142885953	chr4:3669343-3669344	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs533705366	chr4:3669351-3669352	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs545898498	chr4:3669364-3669365	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs562837996	chr4:3669373-3669374	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs182487484	chr4:3669410-3669411	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs548778771	chr4:3669411-3669412	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs548658445	chr4:3669413-3669414	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs57994327	chr4:3669479-3669480	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186847441	chr4:3669485-3669486	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs546908041	chr4:3669507-3669508	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs372949493	chr4:3669529-3669530	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs10033709	chr4:3669544-3669545	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs10010868	chr4:3669550-3669551	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs114726201	chr4:3669577-3669578	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs555883136	chr4:3669587-3669588	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs111713371	chr4:3669605-3669606	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199931632	chr4:3669614-3669615	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116589385	chr4:3669616-3669617	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79316283	chr4:3669617-3669618	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575009145	chr4:3669630-3669631	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74637382	chr4:3669641-3669642	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201802522	chr4:3669642-3669643	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10003063	chr4:3669643-3669644	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62272064	chr4:3669647-3669648	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546136649	chr4:3669654-3669655	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200785734	chr4:3669658-3669659	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113882662	chr4:3669662-3669663	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370096395	chr4:3669663-3669664	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200978030	chr4:3669665-3669666	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10033865	chr4:3669666-3669667	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373938492	chr4:3669693-3669694	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552223406	chr4:3669694-3669695	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12512953	chr4:3669713-3669714	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572714970	chr4:3669714-3669715	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542826359	chr4:3669717-3669718	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546480758	chr4:3669722-3669723	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375049157	chr4:3669728-3669729	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562876251	chr4:3669731-3669732	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576504729	chr4:3669734-3669735	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201495995	chr4:3669751-3669752	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10003213	chr4:3669765-3669766	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs10011139	chr4:3669787-3669788	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3658600-3678000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:3668400-3669800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:3669400-3693400	Weak transcription	Right Atrium	heart
4	chr4:3669600-3670000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:3669800-3670400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:3670000-3677600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:3670400-3671600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:3670800-3671000	ZNF genes & repeats	Lung	lung
9	chr4:3670800-3671200	Bivalent Enhancer	Fetal Muscle Leg	muscle
10	chr4:3670800-3674000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:3671000-3673000	Weak transcription	Lung	lung
12	chr4:3671200-3671400	Enhancers	Brain Anterior Caudate	brain
13	chr4:3671400-3672200	Weak transcription	Brain Anterior Caudate	brain
14	chr4:3671600-3672400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:3672000-3672600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr4:3672200-3672400	Enhancers	Brain Anterior Caudate	brain
17	chr4:3672400-3672800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:3672400-3673400	Weak transcription	Brain Anterior Caudate	brain
19	chr4:3672600-3673000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr4:3672800-3675600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:3673000-3674000	Enhancers	HepG2	liver
22	chr4:3673000-3674200	Enhancers	Pancreas	Pancrea
23	chr4:3673000-3674600	Enhancers	Lung	lung
24	chr4:3673200-3673800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:3673400-3673600	Enhancers	Brain Anterior Caudate	brain
26	chr4:3673400-3674000	Enhancers	A549	lung
27	chr4:3673400-3674200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr4:3673400-3674200	Bivalent Enhancer	Fetal Stomach	stomach
29	chr4:3673400-3674200	Enhancers	Gastric	stomach
30	chr4:3673600-3674400	Enhancers	Hela-S3	cervix
31	chr4:3674000-3674200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr4:3674000-3674200	Bivalent Enhancer	Left Ventricle	heart
33	chr4:3674000-3674200	Flanking Active TSS	A549	lung
34	chr4:3674000-3674200	Flanking Bivalent TSS/Enh	HepG2	liver
35	chr4:3674200-3674400	Bivalent Enhancer	HepG2	liver
36	chr4:3674200-3678800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:3674600-3674800	Weak transcription	Lung	lung
38	chr4:3674800-3676600	Enhancers	Lung	lung
39	chr4:3675600-3675800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:3675600-3676400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr4:3675600-3676600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr4:3675800-3676000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
43	chr4:3675800-3676200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:3676200-3677400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:3676400-3677600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:3677000-3677400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr4:3677000-3677400	Enhancers	Spleen	Spleen
48	chr4:3677200-3677400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:3677200-3677400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr4:3677200-3678400	Bivalent Enhancer	Fetal Muscle Leg	muscle

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