Variant report

Variant	nsv526508
Chromosome Location	chr4:8357923-8371554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:99)
CpG islands
(count:427)
Chromatin interactive
region (count:13)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:99 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:8359490-8359857	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:8359436-8359516	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr4:8369879-8369917	K562	blood:	n/a	n/a
4	CHD1	chr4:8359330-8359337	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr4:8359488-8360184	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:8368600-8368750	SK-N-SH_RA	brain:	n/a	n/a
7	CTCF	chr4:8366700-8366850	GM12878	blood:	n/a	chr4:8366793-8366811 chr4:8366799-8366808
8	E2F4	chr4:8361892-8362092	MCF10A-Er-Src	breast:	n/a	n/a
9	E2F6	chr4:8369784-8369902	K562	blood:	n/a	n/a
10	EGR1	chr4:8359889-8360235	H1-hESC	embryonic stem cell:	n/a	n/a
11	EP300	chr4:8368008-8368418	SK-N-SH_RA	brain:	n/a	chr4:8368362-8368372
12	EP300	chr4:8359445-8360267	H1-hESC	embryonic stem cell:	n/a	n/a
13	EP300	chr4:8359344-8359992	ECC-1	luminal epithelium:	n/a	n/a
14	EP300	chr4:8362586-8362683	K562	blood:	n/a	n/a
15	EP300	chr4:8368085-8368361	SK-N-SH_RA	brain:	n/a	n/a
16	ESR1	chr4:8359445-8359775	ECC-1	luminal epithelium:	n/a	n/a
17	FOS	chr4:8364349-8364547	MCF10A-Er-Src	breast:	n/a	n/a
18	GATA2	chr4:8365254-8365659	HUVEC	blood vessel:	n/a	n/a
19	GTF2F1	chr4:8359620-8359655	H1-hESC	embryonic stem cell:	n/a	n/a
20	IRF1	chr4:8360018-8360079	K562	blood:	n/a	n/a
21	JUND	chr4:8359531-8359689	H1-hESC	embryonic stem cell:	n/a	n/a
22	JUND	chr4:8362551-8362672	K562	blood:	n/a	n/a
23	JUND	chr4:8366221-8366439	HepG2	liver:	n/a	n/a
24	JUND	chr4:8360957-8361245	H1-hESC	embryonic stem cell:	n/a	n/a
25	JUND	chr4:8361013-8361212	H1-hESC	embryonic stem cell:	n/a	n/a
26	JUND	chr4:8359525-8360163	H1-hESC	embryonic stem cell:	n/a	n/a
27	KAP1	chr4:8363279-8364558	K562	blood:	n/a	n/a
28	MAX	chr4:8359499-8360539	H1-hESC	embryonic stem cell:	n/a	n/a
29	MXI1	chr4:8363296-8363445	K562	blood:	n/a	n/a
30	MXI1	chr4:8367607-8368325	SK-N-SH	brain:	n/a	n/a
31	MYC	chr4:8362510-8362627	K562	blood:	n/a	n/a
32	MYC	chr4:8362506-8362698	K562	blood:	n/a	n/a
33	MYC	chr4:8358700-8358786	H1-hESC	embryonic stem cell:	n/a	n/a
34	NANOG	chr4:8359480-8359718	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr4:8359831-8360018	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr4:8366217-8366344	GM12878	blood:	n/a	n/a
37	POLR2A	chr4:8367183-8367246	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr4:8358786-8359092	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr4:8360910-8361296	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr4:8358803-8358992	GM12878	blood:	n/a	n/a
41	POLR2A	chr4:8369445-8369613	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr4:8366203-8366305	ProgFib	skin:	n/a	n/a
43	POLR2A	chr4:8366181-8366188	ProgFib	skin:	n/a	n/a
44	POLR2A	chr4:8361160-8361172	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr4:8367221-8367362	ProgFib	skin:	n/a	n/a
46	POLR2A	chr4:8358658-8358661	Gliobla	brain:	n/a	n/a
47	POLR2A	chr4:8366669-8366702	K562	blood:	n/a	n/a
48	POLR2A	chr4:8361419-8361515	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr4:8363376-8363673	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr4:8366612-8366619	K562	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8359458-8359508	ProgFib	skin:	n/a
2	chr4:8359247-8359297	PANC-1	pancreas:	n/a
3	chr4:8359458-8359508	HNPCEpiC	eye:	n/a
4	chr4:8359458-8359508	GM12892	blood:	n/a
5	chr4:8359269-8359319	SK-N-MC	brain:	n/a
6	chr4:8359269-8359319	NB4	blood:	n/a
7	chr4:8368601-8368651	CMK	blood:	n/a
8	chr4:8359499-8359549	HCPEpiC	choroid plexus:	n/a
9	chr4:8368601-8368651	RPTEC	kidney:	n/a
10	chr4:8359458-8359508	HAEpiC	amniotic membrane:	n/a
11	chr4:8359269-8359319	BE2_C	brain:	n/a
12	chr4:8359269-8359319	GM12892	blood:	n/a
13	chr4:8359458-8359508	HCM	heart:	n/a
14	chr4:8368601-8368651	GM12892	blood:	n/a
15	chr4:8359269-8359319	PFSK-1	brain:	n/a
16	chr4:8359499-8359549	Caco-2	colon:	n/a
17	chr4:8359458-8359508	K562	blood:	n/a
18	chr4:8359499-8359549	AoSMC	blood vessel:	n/a
19	chr4:8359458-8359508	NT2-D1	testis:	n/a
20	chr4:8359458-8359508	HepG2	liver:	n/a
21	chr4:8359247-8359297	SK-N-SH	brain:	n/a
22	chr4:8368486-8368536	H1-hESC	embryonic stem cell:	embryo
23	chr4:8368575-8368625	GM19239	blood:	n/a
24	chr4:8368601-8368651	GM12878	blood:	n/a
25	chr4:8368575-8368625	HUVEC	blood vessel:	n/a
26	chr4:8359458-8359508	MCF-7	breast:	n/a
27	chr4:8368575-8368625	PFSK-1	brain:	n/a
28	chr4:8359269-8359319	GM19239	blood:	n/a
29	chr4:8359458-8359508	HIPEpiC	eye:	n/a
30	chr4:8368601-8368651	MCF-7	breast:	n/a
31	chr4:8368486-8368536	SKMC	muscle:	n/a
32	chr4:8368486-8368536	HCF	heart:	n/a
33	chr4:8368575-8368625	H1-hESC	embryonic stem cell:	embryo
34	chr4:8368575-8368625	HCF	heart:	n/a
35	chr4:8368575-8368625	HRE	kidney:	n/a
36	chr4:8368486-8368536	T-47D	breast:	n/a
37	chr4:8359269-8359319	H1-hESC	embryonic stem cell:	embryo
38	chr4:8359247-8359297	HRE	kidney:	n/a
39	chr4:8359458-8359508	CMK	blood:	n/a
40	chr4:8359247-8359297	PrEC	prostate:	n/a
41	chr4:8359269-8359319	PrEC	prostate:	n/a
42	chr4:8359269-8359319	Hepatocyte	liver:	n/a
43	chr4:8359499-8359549	ovcar-3	ovarian:	n/a
44	chr4:8359247-8359297	SAEC	small airway:	n/a
45	chr4:8368575-8368625	Caco-2	colon:	n/a
46	chr4:8368601-8368651	PFSK-1	brain:	n/a
47	chr4:8368601-8368651	BJ	skin:	n/a
48	chr4:8368486-8368536	MCF10A-Er-Src	breast:	n/a
49	chr4:8359269-8359319	BJ	skin:	n/a
50	chr4:8368575-8368625	GM06990	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
2	chr4:8358055..8360875-chr4:8366726..8369353,3	K562	blood:
3	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
4	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
5	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
6	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
7	chr4:8308134..8310233-chr4:8366379..8367956,2	K562	blood:
8	chr4:8348558..8350885-chr4:8366825..8368402,2	MCF-7	breast:
9	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
10	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:
11	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
12	chr4:8370118..8372500-chr4:8374648..8377546,2	K562	blood:
13	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOX3-5	chr4:8365860-8366475	NONHSAT095091
2	lnc-HTRA3-4	chr4:8358049-8358702	NONHSAT095089
3	lnc-ACOX3-1	chr4:8357038-8359103	ENSG00000251615
4	lnc-ACOX3-1	chr4:8356817-8360065	ENSG00000251615.3
5	lnc-ACOX3-1	chr4:8356817-8359103	NONHSAT095088
6	lnc-ACOX3-5	chr4:8367183-8367485	NONHSAT095091
7	lnc-HTRA3-4	chr4:8358805-8360149	NONHSAT095089

No data

Variant related genes	Relation type
ENSG00000251615	TF binding region
ENSG00000251615	CpG island
ENSG00000087008	chromatin interactions
ENSG00000251615	chromatin interactions

Extended variants
information (count: 690 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12500853	chr4:8357923-8357924	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556412756	chr4:8357954-8357955	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs139738876	chr4:8357955-8357956	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs60387429	chr4:8357970-8357971	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554178589	chr4:8358007-8358008	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs572446433	chr4:8358013-8358014	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs543061368	chr4:8358043-8358044	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs555111958	chr4:8358048-8358049	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs573851394	chr4:8358055-8358056	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs544446408	chr4:8358098-8358099	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs562756337	chr4:8358103-8358104	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs144530800	chr4:8358144-8358145	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs184430631	chr4:8358148-8358149	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs560045601	chr4:8358155-8358156	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs7657076	chr4:8358192-8358193	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs146600045	chr4:8358198-8358199	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs567045141	chr4:8358234-8358235	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs531769915	chr4:8358260-8358261	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs186901766	chr4:8358264-8358265	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs75014689	chr4:8358271-8358272	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs114709672	chr4:8358279-8358280	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs76890796	chr4:8358290-8358291	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs73085853	chr4:8358309-8358310	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs536267727	chr4:8358334-8358335	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs547059630	chr4:8358349-8358350	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs3733532	chr4:8358361-8358362	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs28538757	chr4:8358381-8358382	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs28455691	chr4:8358383-8358384	Bivalent Enhancer Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs28578263	chr4:8358416-8358417	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs576643915	chr4:8358419-8358420	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs28407751	chr4:8358421-8358422	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs28689793	chr4:8358430-8358431	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs535893778	chr4:8358436-8358437	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs28449199	chr4:8358437-8358438	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs554872478	chr4:8358469-8358470	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs143073876	chr4:8358497-8358498	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs569977122	chr4:8358509-8358510	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs577762527	chr4:8358523-8358524	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs545245923	chr4:8358528-8358529	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs537198075	chr4:8358533-8358534	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs558836870	chr4:8358568-8358569	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs183665857	chr4:8358575-8358576	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs188761910	chr4:8358582-8358583	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs560200249	chr4:8358613-8358614	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs189468403	chr4:8358614-8358615	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs545518169	chr4:8358634-8358635	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs79807394	chr4:8358661-8358662	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs78005336	chr4:8358666-8358667	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs201636931	chr4:8358673-8358674	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs77506128	chr4:8358696-8358697	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8351600-8362800	Enhancers	Placenta Amnion	Placenta Amnion
2	chr4:8353400-8366200	Weak transcription	Aorta	Aorta
3	chr4:8353600-8366000	Weak transcription	Brain Hippocampus Middle	brain
4	chr4:8354200-8359400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:8354200-8360000	Weak transcription	Brain Anterior Caudate	brain
6	chr4:8354200-8366200	Weak transcription	Brain Substantia Nigra	brain
7	chr4:8354400-8366000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr4:8354400-8366000	Weak transcription	Brain Angular Gyrus	brain
9	chr4:8354400-8367000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr4:8354400-8367200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr4:8354600-8381000	Weak transcription	Right Atrium	heart
12	chr4:8355000-8358200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:8355000-8366200	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr4:8355200-8358600	Weak transcription	Gastric	stomach
15	chr4:8355400-8365400	Weak transcription	Left Ventricle	heart
16	chr4:8355400-8366000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr4:8355800-8358400	Enhancers	HSMM	muscle
18	chr4:8355800-8358400	Enhancers	HSMMtube	muscle
19	chr4:8355800-8366000	Weak transcription	Lung	lung
20	chr4:8355800-8366200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr4:8355800-8384800	Weak transcription	Fetal Lung	lung
22	chr4:8356000-8358600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:8356200-8358400	Weak transcription	Fetal Thymus	thymus
24	chr4:8356200-8358800	Enhancers	Rectal Smooth Muscle	rectum
25	chr4:8356200-8366200	Weak transcription	Thymus	Thymus
26	chr4:8356400-8360200	Enhancers	HMEC	breast
27	chr4:8356600-8360400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr4:8356800-8358400	Enhancers	Colon Smooth Muscle	Colon
29	chr4:8356800-8360000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:8356800-8360400	Enhancers	NHEK	skin
31	chr4:8357000-8358800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:8357000-8360400	Enhancers	Fetal Stomach	stomach
33	chr4:8357200-8358600	Enhancers	Stomach Smooth Muscle	stomach
34	chr4:8357600-8358000	Enhancers	Fetal Muscle Leg	muscle
35	chr4:8357600-8358600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
36	chr4:8357600-8358600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr4:8357600-8358600	Enhancers	Fetal Heart	heart
38	chr4:8357600-8358600	Enhancers	Fetal Kidney	kidney
39	chr4:8357600-8358800	Enhancers	Right Ventricle	heart
40	chr4:8357600-8359000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr4:8357600-8359400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
42	chr4:8357600-8360200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr4:8357600-8360200	Enhancers	Ovary	ovary
44	chr4:8357600-8360600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr4:8357800-8358000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:8357800-8358000	Enhancers	Placenta	Placenta
47	chr4:8357800-8358200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:8357800-8358200	Bivalent Enhancer	NH-A	brain
49	chr4:8357800-8358400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr4:8357800-8358400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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