Variant report

Variant	nsv878576
Chromosome Location	chr4:7720919-7746820
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:526)
CpG islands
(count:978)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:7721424-7721624	GM12878	blood:	n/a	chr4:7721428-7721444
2	BHLHE40	chr4:7745946-7746146	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:7741755-7741942	K562	blood:	n/a	n/a
4	CBX3	chr4:7739564-7739783	K562	blood:	n/a	n/a
5	CEBPB	chr4:7745489-7745675	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr4:7745484-7745715	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:7721357-7721601	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:7745373-7745789	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr4:7745530-7745746	IMR90	lung:	n/a	n/a
10	CHD2	chr4:7721401-7721673	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr4:7723820-7723970	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:7721393-7721667	Lung_OC	lung:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
13	CTCF	chr4:7723835-7723917	GM19240	blood:	n/a	n/a
14	CTCF	chr4:7721180-7721222	GM19239	blood:	n/a	n/a
15	CTCF	chr4:7723820-7723970	AG09309	skin:	n/a	n/a
16	CTCF	chr4:7721713-7721825	ProgFib	skin:	n/a	n/a
17	CTCF	chr4:7722340-7722490	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr4:7721368-7721611	Fibrobl	skin:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
19	CTCF	chr4:7721400-7721550	Hela-S3	cervix:	n/a	chr4:7721475-7721493
20	CTCF	chr4:7721400-7721550	GM12867	blood:	n/a	chr4:7721475-7721493
21	CTCF	chr4:7723711-7724020	IMR90	lung:	n/a	n/a
22	CTCF	chr4:7721332-7721852	GM12892	blood:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
23	CTCF	chr4:7721420-7721570	GM12869	blood:	n/a	chr4:7721475-7721493
24	CTCF	chr4:7721460-7721610	HEEpiC	esophagus:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
25	CTCF	chr4:7721336-7721655	Pancreas_OC	pancreas:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
26	CTCF	chr4:7721014-7722522	SK-N-SH	brain:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
27	CTCF	chr4:7721308-7721624	A549	lung:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
28	CTCF	chr4:7721277-7721681	HepG2	liver:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
29	CTCF	chr4:7721753-7721838	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr4:7723840-7723990	RPTEC	kidney:	n/a	n/a
31	CTCF	chr4:7721420-7721570	HVMF	connective:	n/a	chr4:7721475-7721493
32	CTCF	chr4:7721440-7721590	GM12878	blood:	n/a	chr4:7721475-7721493
33	CTCF	chr4:7726279-7726445	GM19239	blood:	n/a	n/a
34	CTCF	chr4:7723807-7723974	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:7723797-7723966	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:7726296-7726527	GM12891	blood:	n/a	n/a
37	CTCF	chr4:7721460-7721610	GM12872	blood:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
38	CTCF	chr4:7721740-7721890	GM12871	blood:	n/a	n/a
39	CTCF	chr4:7723780-7723930	HMF	breast:	n/a	n/a
40	CTCF	chr4:7723840-7723990	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr4:7721243-7721706	IMR90	lung:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
42	CTCF	chr4:7721420-7721570	GM12864	blood:	n/a	chr4:7721475-7721493
43	CTCF	chr4:7721420-7721570	HRPEpiC	eye:	n/a	chr4:7721475-7721493
44	CTCF	chr4:7723780-7723930	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr4:7721400-7721550	K562	blood:	n/a	chr4:7721475-7721493
46	CTCF	chr4:7723820-7723970	GM12864	blood:	n/a	n/a
47	CTCF	chr4:7721420-7721570	GM12873	blood:	n/a	chr4:7721475-7721493
48	CTCF	chr4:7721420-7721570	GM12865	blood:	n/a	chr4:7721475-7721493
49	CTCF	chr4:7721420-7721570	GM06990	blood:	n/a	chr4:7721475-7721493
50	CTCF	chr4:7722220-7722370	AoAF	blood vessel:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7721340-7721390	HUVEC	blood vessel:	n/a
2	chr4:7741555-7741605	RPTEC	kidney:	n/a
3	chr4:7721340-7721390	HUVEC	blood vessel:	n/a
4	chr4:7741555-7741605	RPTEC	kidney:	n/a
5	chr4:7739323-7739373	T-47D	breast:	n/a
6	chr4:7738930-7738980	Hela-S3	cervix:	n/a
7	chr4:7721340-7721390	K562	blood:	n/a
8	chr4:7742526-7742576	AG10803	skin:	n/a
9	chr4:7721563-7721613	AG09309	skin:	n/a
10	chr4:7735312-7735362	HCF	heart:	n/a
11	chr4:7736753-7736803	BJ	skin:	n/a
12	chr4:7721340-7721390	MCF-7	breast:	n/a
13	chr4:7740821-7740871	SKMC	muscle:	n/a
14	chr4:7741555-7741605	NT2-D1	testis:	n/a
15	chr4:7736753-7736803	AG10803	skin:	n/a
16	chr4:7741555-7741605	AG09319	gingival:	n/a
17	chr4:7741555-7741605	H1-hESC	embryonic stem cell:	embryo
18	chr4:7740821-7740871	BJ	skin:	n/a
19	chr4:7721563-7721613	SAEC	small airway:	n/a
20	chr4:7738930-7738980	SK-N-SH_RA	brain:	n/a
21	chr4:7736057-7736107	HAEpiC	amniotic membrane:	n/a
22	chr4:7740821-7740871	Hela-S3	cervix:	n/a
23	chr4:7736753-7736803	HCT-116	colon:	n/a
24	chr4:7721563-7721613	U87	brain:	n/a
25	chr4:7740427-7740477	NB4	blood:	n/a
26	chr4:7721340-7721390	PANC-1	pancreas:	n/a
27	chr4:7739323-7739373	GM12891	blood:	n/a
28	chr4:7739323-7739373	PFSK-1	brain:	n/a
29	chr4:7741680-7741730	Hela-S3	cervix:	n/a
30	chr4:7736753-7736803	AG04450	lung:	fetal
31	chr4:7721340-7721390	NH-A	brain:	n/a
32	chr4:7735312-7735362	SKMC	muscle:	n/a
33	chr4:7740503-7740553	HMEC	breast:	n/a
34	chr4:7736302-7736352	NT2-D1	testis:	n/a
35	chr4:7741680-7741730	HIPEpiC	eye:	n/a
36	chr4:7739323-7739373	HCF	heart:	n/a
37	chr4:7742291-7742341	AoSMC	blood vessel:	n/a
38	chr4:7741680-7741730	PFSK-1	brain:	n/a
39	chr4:7739323-7739373	PrEC	prostate:	n/a
40	chr4:7721340-7721390	A549	lung:	n/a
41	chr4:7739323-7739373	NT2-D1	testis:	n/a
42	chr4:7736753-7736803	SKMC	muscle:	n/a
43	chr4:7736302-7736352	A549	lung:	n/a
44	chr4:7740503-7740553	GM12891	blood:	n/a
45	chr4:7740503-7740553	AG09309	skin:	n/a
46	chr4:7735312-7735362	AG09319	gingival:	n/a
47	chr4:7736057-7736107	HL-60	blood:	n/a
48	chr4:7742291-7742341	AG09309	skin:	n/a
49	chr4:7740427-7740477	GM19239	blood:	n/a
50	chr4:7742526-7742576	GM12878	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7716222..7719124-chr4:7719418..7721619,2	MCF-7	breast:
2	chr4:7464162..7464863-chr4:7721037..7721847,3	MCF-7	breast:
3	chr4:7717845..7720426-chr4:7722093..7724959,2	K562	blood:
4	chr4:7720870..7722721-chr4:7731493..7735156,3	MCF-7	breast:
5	chr4:7724746..7727084-chr4:7966375..7967893,2	K562	blood:
6	chr4:7738338..7740956-chr4:7755052..7757253,2	K562	blood:
7	chr4:7524845..7525381-chr4:7721481..7722229,2	K562	blood:
8	chr4:7739904..7741898-chr4:7754670..7757440,2	K562	blood:
9	chr4:7705546..7706171-chr4:7721058..7721957,2	MCF-7	breast:
10	chr4:7717399..7719546-chr4:7720941..7723402,3	K562	blood:
11	chr4:7720870..7722721-chr4:7731493..7735156,3	MCF-7	breast:
12	chr4:7556325..7556952-chr4:7720957..7721491,2	MCF-7	breast:
13	chr4:7729339..7732092-chr4:7733830..7736554,3	K562	blood:
14	chr4:7193893..7194671-chr4:7721003..7721515,2	K562	blood:
15	chr4:7723319..7725071-chr4:7788895..7790676,2	K562	blood:
16	chr4:7723652..7724312-chr4:7988958..7989693,2	MCF-7	breast:

No data

Variant related genes	Relation type
SORCS2	TF binding region
SORCS2	CpG island
ENSG00000272620	chromatin interactions
ENSG00000184985	chromatin interactions

Extended variants
information (count: 1631 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1631 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4689839	chr4:7720919-7720920	Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371008816	chr4:7720934-7720935	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545451270	chr4:7720948-7720949	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140873065	chr4:7720954-7720955	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572083982	chr4:7720985-7720986	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75774408	chr4:7721016-7721017	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368262801	chr4:7721019-7721020	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561233939	chr4:7721043-7721044	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs79185899	chr4:7721048-7721049	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531844665	chr4:7721146-7721147	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534578825	chr4:7721166-7721167	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs58280827	chr4:7721167-7721168	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs397970379	chr4:7721168-7721169	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10022742	chr4:7721199-7721200	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565447897	chr4:7721227-7721228	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532631316	chr4:7721247-7721248	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs551435853	chr4:7721251-7721252	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs142784481	chr4:7721264-7721265	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs61067913	chr4:7721288-7721289	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10001090	chr4:7721307-7721308	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs11934102	chr4:7721317-7721318	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs538112470	chr4:7721323-7721324	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556201186	chr4:7721329-7721330	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577751213	chr4:7721330-7721331	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556829220	chr4:7721358-7721359	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10001165	chr4:7721361-7721362	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572243304	chr4:7721378-7721379	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542721449	chr4:7721386-7721387	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs371782150	chr4:7721391-7721392	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576048875	chr4:7721393-7721394	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs144744381	chr4:7721394-7721395	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544058182	chr4:7721408-7721409	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35190239	chr4:7721412-7721413	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565469072	chr4:7721414-7721415	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs367724343	chr4:7721416-7721417	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs116472266	chr4:7721429-7721430	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs115618323	chr4:7721443-7721444	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201516993	chr4:7721459-7721460	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs559906358	chr4:7721460-7721461	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs538090545	chr4:7721489-7721490	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs549123676	chr4:7721495-7721496	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116154256	chr4:7721516-7721517	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376199834	chr4:7721545-7721546	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112966663	chr4:7721554-7721555	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147416784	chr4:7721580-7721581	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571495390	chr4:7721608-7721609	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139129467	chr4:7721618-7721619	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553642494	chr4:7721702-7721703	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576948275	chr4:7721710-7721711	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565541411	chr4:7721714-7721715	Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7686200-7721000	Weak transcription	Brain Anterior Caudate	brain
2	chr4:7699400-7721200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr4:7713400-7721000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:7716400-7721200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:7716400-7721200	Weak transcription	Ovary	ovary
6	chr4:7716600-7721200	Weak transcription	Brain Germinal Matrix	brain
7	chr4:7717000-7726200	Weak transcription	Brain Substantia Nigra	brain
8	chr4:7717600-7723000	Weak transcription	Right Atrium	heart
9	chr4:7717800-7739200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:7718000-7721200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr4:7718600-7729000	Weak transcription	Brain Angular Gyrus	brain
12	chr4:7720000-7721000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:7720000-7721200	Weak transcription	Brain Hippocampus Middle	brain
14	chr4:7720400-7721400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
15	chr4:7720800-7721200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr4:7720800-7721200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
17	chr4:7721000-7721200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:7721000-7721200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:7721000-7721200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr4:7721000-7721200	Bivalent Enhancer	Fetal Muscle Leg	muscle
21	chr4:7721000-7721200	Enhancers	Gastric	stomach
22	chr4:7721000-7721200	Active TSS	HepG2	liver
23	chr4:7721000-7721400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr4:7721000-7721600	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr4:7721000-7721600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr4:7721000-7721800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:7721000-7721800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:7721000-7721800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:7721000-7721800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:7721000-7721800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr4:7721000-7721800	Enhancers	Brain Anterior Caudate	brain
32	chr4:7721000-7721800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
33	chr4:7721200-7721400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:7721200-7721400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
35	chr4:7721200-7721400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
36	chr4:7721200-7721400	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
37	chr4:7721200-7721400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr4:7721200-7721400	Enhancers	Brain Cingulate Gyrus	brain
39	chr4:7721200-7721400	Bivalent Enhancer	Colonic Mucosa	Colon
40	chr4:7721200-7721400	Enhancers	Colon Smooth Muscle	Colon
41	chr4:7721200-7721400	Bivalent Enhancer	Fetal Intestine Large	intestine
42	chr4:7721200-7721400	Bivalent Enhancer	Fetal Intestine Small	intestine
43	chr4:7721200-7721400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
44	chr4:7721200-7721400	Bivalent Enhancer	Fetal Stomach	stomach
45	chr4:7721200-7721400	Enhancers	Left Ventricle	heart
46	chr4:7721200-7721400	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
47	chr4:7721200-7721400	Flanking Active TSS	HepG2	liver
48	chr4:7721200-7721600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr4:7721200-7721600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:7721200-7721600	Enhancers	Brain Hippocampus Middle	brain

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