Variant report

Variant	nsv593628
Chromosome Location	chr4:8254784-8320126
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1509)
CpG islands
(count:2199)
Chromatin interactive
region (count:63)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1509 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8268932-8269253	K562	blood:	n/a	n/a
2	ARID3A	chr4:8305348-8305642	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:8305135-8305823	K562	blood:	n/a	n/a
4	ATF1	chr4:8254361-8254786	K562	blood:	n/a	n/a
5	ATF1	chr4:8305288-8305697	K562	blood:	n/a	n/a
6	ATF3	chr4:8305246-8305673	K562	blood:	n/a	n/a
7	BACH1	chr4:8300502-8300525	K562	blood:	n/a	n/a
8	BACH1	chr4:8307134-8307192	K562	blood:	n/a	n/a
9	BACH1	chr4:8317763-8317973	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:8304571-8306375	K562	blood:	n/a	n/a
11	BACH1	chr4:8305142-8305898	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:8319138-8319178	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:8304810-8304892	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr4:8305288-8305655	GM12878	blood:	n/a	n/a
15	BCL3	chr4:8305176-8305795	A549	lung:	n/a	n/a
16	BCL3	chr4:8305344-8305701	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:8289208-8289321	K562	blood:	n/a	n/a
18	BHLHE40	chr4:8279249-8279980	K562	blood:	n/a	n/a
19	BHLHE40	chr4:8265162-8265446	K562	blood:	n/a	n/a
20	BHLHE40	chr4:8317142-8317955	HepG2	liver:	n/a	n/a
21	BHLHE40	chr4:8287038-8287334	HepG2	liver:	n/a	n/a
22	BHLHE40	chr4:8305090-8305693	K562	blood:	n/a	n/a
23	BHLHE40	chr4:8280255-8280943	K562	blood:	n/a	chr4:8280853-8280862 chr4:8280854-8280863 chr4:8280852-8280865 chr4:8280854-8280863
24	BHLHE40	chr4:8299557-8299753	K562	blood:	n/a	n/a
25	BHLHE40	chr4:8285389-8285828	K562	blood:	n/a	n/a
26	BHLHE40	chr4:8317095-8317954	K562	blood:	n/a	n/a
27	BHLHE40	chr4:8287053-8287262	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:8317386-8317761	A549	lung:	n/a	n/a
29	BHLHE40	chr4:8268745-8269240	K562	blood:	n/a	chr4:8269078-8269094
30	BHLHE40	chr4:8265116-8265491	HepG2	liver:	n/a	n/a
31	BHLHE40	chr4:8254185-8254854	K562	blood:	n/a	n/a
32	BHLHE40	chr4:8311040-8311321	K562	blood:	n/a	chr4:8311061-8311077
33	BHLHE40	chr4:8276763-8276886	K562	blood:	n/a	n/a
34	BHLHE40	chr4:8313423-8313620	K562	blood:	n/a	n/a
35	BHLHE40	chr4:8305905-8306248	K562	blood:	n/a	n/a
36	BHLHE40	chr4:8286938-8287401	K562	blood:	n/a	n/a
37	BHLHE40	chr4:8260314-8260592	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:8260365-8260601	K562	blood:	n/a	n/a
39	BHLHE40	chr4:8273045-8273305	K562	blood:	n/a	n/a
40	BRCA1	chr4:8268932-8269205	HepG2	liver:	n/a	n/a
41	BRCA1	chr4:8269017-8269224	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr4:8305162-8305645	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr4:8305223-8305739	K562	blood:	n/a	n/a
44	CBX3	chr4:8305032-8305869	K562	blood:	n/a	n/a
45	CCNT2	chr4:8283301-8283510	K562	blood:	n/a	n/a
46	CCNT2	chr4:8308348-8308555	K562	blood:	n/a	n/a
47	CCNT2	chr4:8299683-8299875	K562	blood:	n/a	n/a
48	CCNT2	chr4:8305109-8305716	K562	blood:	n/a	chr4:8305145-8305154
49	CCNT2	chr4:8254130-8254835	K562	blood:	n/a	n/a
50	CCNT2	chr4:8268882-8269163	K562	blood:	n/a	chr4:8269023-8269032

(count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8262942-8262992	HUVEC	blood vessel:	n/a
2	chr4:8262942-8262992	SKMC	muscle:	n/a
3	chr4:8256393-8256443	NHDF-neo	bronchial:	n/a
4	chr4:8262942-8262992	HUVEC	blood vessel:	n/a
5	chr4:8262942-8262992	SKMC	muscle:	n/a
6	chr4:8256393-8256443	NHDF-neo	bronchial:	n/a
7	chr4:8270795-8270845	GM06990	blood:	n/a
8	chr4:8305940-8305990	HCM	heart:	n/a
9	chr4:8317995-8318045	HEEpiC	esophagus:	n/a
10	chr4:8292202-8292252	GM12878	blood:	n/a
11	chr4:8263073-8263123	BE2_C	brain:	n/a
12	chr4:8308672-8308722	HUVEC	blood vessel:	n/a
13	chr4:8317995-8318045	HEK293	kidney:	embryo
14	chr4:8262659-8262709	GM12891	blood:	n/a
15	chr4:8270795-8270845	CMK	blood:	n/a
16	chr4:8308672-8308722	NT2-D1	testis:	n/a
17	chr4:8307757-8307807	GM12878	blood:	n/a
18	chr4:8279150-8279200	HRE	kidney:	n/a
19	chr4:8308063-8308113	HEK293	kidney:	embryo
20	chr4:8271507-8271557	GM12891	blood:	n/a
21	chr4:8271319-8271369	Jurkat	blood:	n/a
22	chr4:8317995-8318045	Caco-2	colon:	n/a
23	chr4:8271196-8271246	ECC-1	luminal epithelium:	n/a
24	chr4:8263007-8263057	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:8270795-8270845	SK-N-MC	brain:	n/a
26	chr4:8268962-8269012	Jurkat	blood:	n/a
27	chr4:8271507-8271557	Hela-S3	cervix:	n/a
28	chr4:8307813-8307863	HEK293	kidney:	embryo
29	chr4:8279150-8279200	CMK	blood:	n/a
30	chr4:8271369-8271419	HEK293	kidney:	embryo
31	chr4:8307813-8307863	RPTEC	kidney:	n/a
32	chr4:8262659-8262709	HIPEpiC	eye:	n/a
33	chr4:8291937-8291987	GM19239	blood:	n/a
34	chr4:8271236-8271286	ECC-1	luminal epithelium:	n/a
35	chr4:8299814-8299864	ECC-1	luminal epithelium:	n/a
36	chr4:8256393-8256443	SKMC	muscle:	n/a
37	chr4:8271507-8271557	Jurkat	blood:	n/a
38	chr4:8307888-8307938	SKMC	muscle:	n/a
39	chr4:8279150-8279200	Jurkat	blood:	n/a
40	chr4:8262589-8262639	MCF-7	breast:	n/a
41	chr4:8270795-8270845	NHDF-neo	bronchial:	n/a
42	chr4:8262589-8262639	HIPEpiC	eye:	n/a
43	chr4:8263073-8263123	HRE	kidney:	n/a
44	chr4:8271792-8271842	HRCEpiC	kidney:	n/a
45	chr4:8262659-8262709	HAEpiC	amniotic membrane:	n/a
46	chr4:8271196-8271246	HRPEpiC	eye:	n/a
47	chr4:8305940-8305990	NT2-D1	testis:	n/a
48	chr4:8271414-8271464	U87	brain:	n/a
49	chr4:8308672-8308722	ovcar-3	ovarian:	n/a
50	chr4:8271391-8271441	AG10803	skin:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:8281411..8283569-chr4:8285664..8289042,3	MCF-7	breast:
2	chr4:8298648..8301351-chr4:8301650..8306230,4	K562	blood:
3	chr4:8285233..8287238-chr4:8291804..8293316,2	K562	blood:
4	chr4:8276309..8277181-chr4:8404667..8405454,2	MCF-7	breast:
5	chr4:8281411..8283569-chr4:8285664..8289042,3	MCF-7	breast:
6	chr4:8261994..8265646-chr4:8266271..8270310,6	MCF-7	breast:
7	chr4:8285233..8287238-chr4:8291804..8293316,2	K562	blood:
8	chr4:8276769..8277333-chr4:8404587..8405165,2	K562	blood:
9	chr4:8242105..8244343-chr4:8260959..8263973,3	MCF-7	breast:
10	chr4:8268241..8269567-chr4:8404622..8405485,4	MCF-7	breast:
11	chr4:8271372..8272005-chr5:137514142..137514696,2	NB4	blood:
12	chr4:8296392..8301185-chr4:8301650..8305548,7	K562	blood:
13	chr4:8303617..8305448-chr4:8311831..8313564,2	MCF-7	breast:
14	chr4:8261913..8264810-chr4:8267913..8270603,2	K562	blood:
15	chr4:8252135..8255007-chr4:8262927..8264616,3	K562	blood:
16	chr16:28834863..28835527-chr4:8271061..8271579,2	NB4	blood:
17	chr4:8262200..8264510-chr4:8428848..8430829,2	MCF-7	breast:
18	chr4:8276758..8278622-chr4:8279545..8282150,2	MCF-7	breast:
19	chr4:8280226..8283020-chr4:8285695..8288217,2	K562	blood:
20	chr4:8254660..8257385-chr4:8260489..8263167,2	MCF-7	breast:
21	chr4:8315694..8318647-chr4:8336893..8339393,2	K562	blood:
22	chr4:8254660..8257385-chr4:8260489..8263167,2	MCF-7	breast:
23	chr4:8268620..8269557-chr4:8404343..8405485,5	K562	blood:
24	chr4:8306129..8312354-chr4:8314662..8318399,6	MCF-7	breast:
25	chr4:8286640..8289515-chr4:8304226..8307184,3	K562	blood:
26	chr4:8271058..8271580-chr5:74632260..74632932,2	NB4	blood:
27	chr4:8306129..8312354-chr4:8314662..8318399,6	MCF-7	breast:
28	chr4:8312041..8314245-chr4:8317234..8319161,2	K562	blood:
29	chr4:8261537..8264221-chr4:8264274..8265849,2	MCF-7	breast:
30	chr4:8268637..8269538-chr4:8412094..8412713,3	MCF-7	breast:
31	chr10:105156345..105156947-chr4:8271069..8272007,2	NB4	blood:
32	chr4:8268593..8269552-chr4:8403907..8405561,11	MCF-7	breast:
33	chr4:8311363..8313807-chr4:8315101..8317109,2	K562	blood:
34	chr4:8268685..8271204-chr4:8420095..8422355,2	MCF-7	breast:
35	chr4:8266213..8269192-chr4:8274192..8276756,2	K562	blood:
36	chr4:8308134..8310233-chr4:8366379..8367956,2	K562	blood:
37	chr4:8263022..8264524-chr4:8271054..8272671,2	MCF-7	breast:
38	chr4:8303617..8305448-chr4:8311831..8313564,2	MCF-7	breast:
39	chr4:8276397..8277253-chr4:8404609..8405203,3	MCF-7	breast:
40	chr4:8261913..8264810-chr4:8267913..8270603,2	K562	blood:
41	chr4:8268867..8271118-chr4:8273119..8275755,2	MCF-7	breast:
42	chr4:8296392..8301185-chr4:8301650..8305548,7	K562	blood:
43	chr4:8261994..8265646-chr4:8266271..8270310,6	MCF-7	breast:
44	chr4:8298648..8301351-chr4:8301650..8306230,4	K562	blood:
45	chr4:8286640..8289515-chr4:8304226..8307184,3	K562	blood:
46	chr4:8312041..8314245-chr4:8317234..8319161,2	K562	blood:
47	chr4:8292974..8294945-chr4:8297191..8300156,2	MCF-7	breast:
48	chr4:8252940..8255402-chr4:8411571..8414054,2	K562	blood:
49	chr4:8280226..8283020-chr4:8285695..8288217,2	K562	blood:
50	chr4:8292974..8294945-chr4:8297191..8300156,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HTRA3	hsa-miR-124-3p	chr4:8297797-8297818

Variant related genes	Relation type
ENSG00000249145	TF binding region
ENSG00000248986	TF binding region
HTRA3	TF binding region
ENSG00000249145	CpG island
ENSG00000248986	CpG island
HTRA3	CpG island
ENSG00000112984	chromatin interactions
ENSG00000169714	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000125089	chromatin interactions
ENSG00000112983	chromatin interactions
ENSG00000170801	chromatin interactions
ENSG00000148843	chromatin interactions
ENSG00000168488	chromatin interactions
ENSG00000247372	chromatin interactions

Extended variants
information (count: 3384 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3384 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1678336	chr4:8254784-8254785	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527482596	chr4:8254786-8254787	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112119054	chr4:8254792-8254793	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187724941	chr4:8254848-8254849	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs192340977	chr4:8254918-8254919	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs140067333	chr4:8254953-8254954	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs549828985	chr4:8254958-8254959	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs571242187	chr4:8254979-8254980	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs538321019	chr4:8254985-8254986	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs184675930	chr4:8255006-8255007	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs566094163	chr4:8255066-8255067	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs536494484	chr4:8255083-8255084	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs554834135	chr4:8255098-8255099	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs1678335	chr4:8255104-8255105	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs537028271	chr4:8255126-8255127	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs116348938	chr4:8255127-8255128	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs577186784	chr4:8255135-8255136	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs541128170	chr4:8255147-8255148	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs370084596	chr4:8255167-8255168	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs530843573	chr4:8255202-8255203	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs115723336	chr4:8255212-8255213	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs542876127	chr4:8255258-8255259	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs549061276	chr4:8255320-8255321	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs188742505	chr4:8255367-8255368	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs373930146	chr4:8255378-8255379	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs543679759	chr4:8255391-8255392	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs116029666	chr4:8255423-8255424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59269679	chr4:8255450-8255451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397954496	chr4:8255459-8255460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200367425	chr4:8255460-8255461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201186906	chr4:8255461-8255462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550436325	chr4:8255510-8255511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571965257	chr4:8255515-8255516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144946243	chr4:8255537-8255538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192643276	chr4:8255553-8255554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565808758	chr4:8255576-8255577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530217300	chr4:8255612-8255613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372632198	chr4:8255613-8255614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10755198	chr4:8255674-8255675	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs184263434	chr4:8255720-8255721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188998727	chr4:8255771-8255772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115067850	chr4:8255781-8255782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114106001	chr4:8255820-8255821	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535056128	chr4:8255825-8255826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553174761	chr4:8255832-8255833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575012029	chr4:8255835-8255836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370573479	chr4:8255857-8255858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554769949	chr4:8255882-8255883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567702306	chr4:8255888-8255889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6837910	chr4:8255952-8255953	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:57)

Disease	PMID	Source
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
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
Oligozoospermia	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1602 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8245000-8255800	Weak transcription	HMEC	breast
2	chr4:8245200-8255200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:8249800-8257200	Weak transcription	HSMM	muscle
4	chr4:8249800-8268400	Weak transcription	Right Atrium	heart
5	chr4:8249800-8268600	Weak transcription	Fetal Intestine Small	intestine
6	chr4:8250000-8257600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr4:8250600-8261800	Weak transcription	A549	lung
8	chr4:8253000-8256000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:8253200-8256200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr4:8253200-8256800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:8253400-8257600	Weak transcription	Adipose Nuclei	Adipose
12	chr4:8253600-8256400	Enhancers	Placenta	Placenta
13	chr4:8253600-8257400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:8254000-8255200	Enhancers	K562	blood
15	chr4:8254200-8254800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:8254200-8255000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:8254200-8255200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr4:8254200-8255200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:8254200-8255400	Bivalent Enhancer	HepG2	liver
20	chr4:8254200-8256000	Enhancers	Primary hematopoietic stem cells	blood
21	chr4:8254400-8254800	Enhancers	Fetal Lung	lung
22	chr4:8254400-8254800	Enhancers	Gastric	stomach
23	chr4:8254400-8254800	Enhancers	Placenta Amnion	Placenta Amnion
24	chr4:8254400-8255000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:8254400-8255200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:8254400-8255200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:8254400-8255400	Enhancers	Fetal Thymus	thymus
28	chr4:8254600-8254800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr4:8254600-8258000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr4:8254800-8259000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:8254800-8271600	Weak transcription	Gastric	stomach
32	chr4:8255000-8255200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:8255000-8261800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr4:8255200-8256400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:8255200-8259600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr4:8255200-8259600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:8255400-8255800	Weak transcription	Fetal Thymus	thymus
38	chr4:8255800-8256000	Enhancers	Fetal Thymus	thymus
39	chr4:8255800-8256200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:8255800-8256200	Enhancers	Esophagus	oesophagus
41	chr4:8255800-8256400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:8255800-8256400	Enhancers	NHEK	skin
43	chr4:8255800-8256600	Enhancers	HMEC	breast
44	chr4:8256000-8256200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:8256000-8259600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr4:8256000-8260400	Weak transcription	Fetal Thymus	thymus
47	chr4:8256000-8264800	Enhancers	Fetal Muscle Leg	muscle
48	chr4:8256200-8257600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:8256200-8257600	Weak transcription	Esophagus	oesophagus
50	chr4:8256200-8257800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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