Variant report

Variant	nsv878567
Chromosome Location	chr4:7456717-7544610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:616)
CpG islands
(count:2322)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:7517343-7517590	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:7532753-7532902	HepG2	liver:	n/a	n/a
3	ATF3	chr4:7462396-7462591	K562	blood:	n/a	chr4:7462510-7462519
4	BACH1	chr4:7459110-7459520	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:7474386-7474403	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr4:7544346-7544668	GM12878	blood:	n/a	n/a
7	BCL3	chr4:7544248-7544648	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:7463215-7463337	K562	blood:	n/a	chr4:7463252-7463273 chr4:7463259-7463268
9	BHLHE40	chr4:7462305-7462695	HepG2	liver:	n/a	chr4:7462508-7462521 chr4:7462511-7462520 chr4:7462510-7462519 chr4:7462509-7462518 chr4:7462510-7462519 chr4:7462504-7462525
10	BHLHE40	chr4:7462352-7462679	K562	blood:	n/a	chr4:7462508-7462521 chr4:7462511-7462520 chr4:7462510-7462519 chr4:7462509-7462518 chr4:7462510-7462519 chr4:7462504-7462525
11	CCNT2	chr4:7505792-7505967	K562	blood:	n/a	n/a
12	CEBPB	chr4:7517279-7517633	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:7517278-7517645	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:7525842-7526080	A549	lung:	n/a	chr4:7525982-7525993
15	CEBPB	chr4:7517322-7517536	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:7525887-7526098	H1-hESC	embryonic stem cell:	n/a	chr4:7525982-7525993
17	CEBPB	chr4:7541525-7541851	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:7472785-7473103	MCF-7	breast:	n/a	n/a
19	CEBPB	chr4:7525826-7526412	HepG2	liver:	n/a	chr4:7525982-7525993
20	CEBPB	chr4:7517417-7517597	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:7517192-7517635	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:7525934-7526014	IMR90	lung:	n/a	chr4:7525982-7525993
23	CEBPB	chr4:7462372-7462637	HepG2	liver:	n/a	n/a
24	CEBPD	chr4:7517347-7517719	HepG2	liver:	n/a	n/a
25	CEBPD	chr4:7516506-7516755	HepG2	liver:	n/a	n/a
26	CEBPZ	chr4:7539713-7539730	HepG2	liver:	n/a	n/a
27	CHD2	chr4:7525404-7525516	HepG2	liver:	n/a	n/a
28	CHD2	chr4:7541279-7542165	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr4:7517348-7517609	HepG2	liver:	n/a	n/a
30	CHD2	chr4:7464210-7464433	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr4:7533508-7533553	HepG2	liver:	n/a	n/a
32	CHD2	chr4:7541538-7541632	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr4:7533892-7533972	HepG2	liver:	n/a	n/a
34	CREB1	chr4:7512161-7512419	A549	lung:	n/a	n/a
35	CTBP2	chr4:7465845-7466283	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:7464220-7464370	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr4:7463040-7463190	WERI-Rb-1	eye:	n/a	chr4:7463085-7463094
38	CTCF	chr4:7464240-7464390	HEK293	kidney:	n/a	n/a
39	CTCF	chr4:7526025-7526108	HepG2	liver:	n/a	n/a
40	CTCF	chr4:7464223-7464470	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:7476140-7476290	HEK293	kidney:	n/a	chr4:7476252-7476261 chr4:7476252-7476265 chr4:7476249-7476267
42	CTCF	chr4:7536260-7536410	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr4:7521739-7521855	HepG2	liver:	n/a	n/a
44	CTCF	chr4:7528320-7528470	A549	lung:	n/a	n/a
45	CTCF	chr4:7500760-7500804	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:7542000-7542150	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:7464460-7464610	AG04449	skin:	n/a	n/a
48	CTCF	chr4:7476180-7476330	WERI-Rb-1	eye:	n/a	chr4:7476252-7476261 chr4:7476252-7476265 chr4:7476249-7476267
49	CTCF	chr4:7462920-7463070	HCM	heart:	n/a	n/a
50	CTCF	chr4:7472468-7472534	GM12892	blood:	n/a	n/a

(count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7528947-7528997	IMR90	lung:	fetal
2	chr4:7533191-7533241	MCF-7	breast:	n/a
3	chr4:7463007-7463057	ECC-1	luminal epithelium:	n/a
4	chr4:7526671-7526721	U87	brain:	n/a
5	chr4:7528947-7528997	IMR90	lung:	fetal
6	chr4:7533191-7533241	MCF-7	breast:	n/a
7	chr4:7463007-7463057	ECC-1	luminal epithelium:	n/a
8	chr4:7526671-7526721	U87	brain:	n/a
9	chr4:7518360-7518410	SK-N-SH	brain:	n/a
10	chr4:7508044-7508094	PANC-1	pancreas:	n/a
11	chr4:7484382-7484432	AG09309	skin:	n/a
12	chr4:7463234-7463284	AG04449	skin:	fetal
13	chr4:7512278-7512328	GM12878	blood:	n/a
14	chr4:7518783-7518833	GM06990	blood:	n/a
15	chr4:7462468-7462518	NB4	blood:	n/a
16	chr4:7528296-7528346	SK-N-SH_RA	brain:	n/a
17	chr4:7483577-7483627	AoSMC	blood vessel:	n/a
18	chr4:7512425-7512475	ECC-1	luminal epithelium:	n/a
19	chr4:7512177-7512227	MCF-7	breast:	n/a
20	chr4:7526671-7526721	ProgFib	skin:	n/a
21	chr4:7502429-7502479	HIPEpiC	eye:	n/a
22	chr4:7528468-7528518	IMR90	lung:	fetal
23	chr4:7508044-7508094	BE2_C	brain:	n/a
24	chr4:7502706-7502756	BJ	skin:	n/a
25	chr4:7526639-7526689	HepG2	liver:	n/a
26	chr4:7511100-7511150	HMEC	breast:	n/a
27	chr4:7472958-7473008	SK-N-MC	brain:	n/a
28	chr4:7512425-7512475	HRPEpiC	eye:	n/a
29	chr4:7518783-7518833	AG04450	lung:	fetal
30	chr4:7526521-7526571	IMR90	lung:	fetal
31	chr4:7502429-7502479	BJ	skin:	n/a
32	chr4:7486772-7486822	MCF10A-Er-Src	breast:	n/a
33	chr4:7511100-7511150	T-47D	breast:	n/a
34	chr4:7463234-7463284	HNPCEpiC	eye:	n/a
35	chr4:7463234-7463284	ProgFib	skin:	n/a
36	chr4:7518783-7518833	NHDF-neo	bronchial:	n/a
37	chr4:7518360-7518410	HMEC	breast:	n/a
38	chr4:7502947-7502997	A549	lung:	n/a
39	chr4:7512177-7512227	SK-N-SH	brain:	n/a
40	chr4:7472958-7473008	NH-A	brain:	n/a
41	chr4:7528947-7528997	SK-N-SH_RA	brain:	n/a
42	chr4:7486772-7486822	GM12892	blood:	n/a
43	chr4:7518783-7518833	AG09309	skin:	n/a
44	chr4:7512016-7512066	NH-A	brain:	n/a
45	chr4:7472958-7473008	BE2_C	brain:	n/a
46	chr4:7512498-7512548	HCT-116	colon:	n/a
47	chr4:7462664-7462714	BJ	skin:	n/a
48	chr4:7485948-7485998	Caco-2	colon:	n/a
49	chr4:7463007-7463057	HCM	heart:	n/a
50	chr4:7512278-7512328	K562	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7513451..7515620-chr4:7531524..7533326,2	K562	blood:
2	chr4:7529694..7531413-chr4:7534964..7537319,2	K562	blood:
3	chr4:7444681..7447159-chr4:7457852..7459823,2	MCF-7	breast:
4	chr4:7524845..7525381-chr4:7721481..7722229,2	K562	blood:
5	chr4:7535311..7535864-chr4:7556278..7556945,2	MCF-7	breast:
6	chr4:7396272..7396793-chr4:7463896..7464564,2	MCF-7	breast:
7	chr4:7455060..7457538-chr4:7459563..7461357,2	K562	blood:
8	chr4:7529694..7531413-chr4:7534964..7537319,2	K562	blood:
9	chr12:13044402..13044911-chr4:7539151..7539651,2	Hela-S3	cervix:
10	chr4:7452936..7455745-chr4:7457448..7459365,2	MCF-7	breast:
11	chr4:7474972..7476940-chr4:7478120..7479939,2	MCF-7	breast:
12	chr4:7524802..7527211-chr4:7527477..7529278,2	MCF-7	breast:
13	chr4:7512552..7515805-chr4:7517576..7521782,4	MCF-7	breast:
14	chr4:7509518..7511220-chr4:7514824..7517339,2	K562	blood:
15	chr4:7540632..7544452-chr4:7547712..7552910,6	MCF-7	breast:
16	chr4:7464162..7464863-chr4:7721037..7721847,3	MCF-7	breast:
17	chr4:7513451..7515620-chr4:7531524..7533326,2	K562	blood:
18	chr4:7516092..7517714-chr4:7519119..7521315,2	K562	blood:
19	chr4:7543788..7545988-chr4:7546899..7549006,2	K562	blood:
20	chr4:7509518..7511220-chr4:7514824..7517339,2	K562	blood:
21	chr15:41624966..41625477-chr4:7539151..7539651,2	Hela-S3	cervix:
22	chr4:7520525..7523407-chr4:7542100..7544094,2	K562	blood:
23	chr4:7512552..7515805-chr4:7517576..7521782,4	MCF-7	breast:
24	chr4:7516846..7519696-chr4:7521879..7524111,2	K562	blood:
25	chr4:7475842..7476773-chr4:7652108..7653034,2	MCF-7	breast:
26	chr4:7534680..7537272-chr4:7547399..7550073,2	MCF-7	breast:
27	chr4:7474972..7476940-chr4:7478120..7479939,2	MCF-7	breast:
28	chr4:7520525..7523407-chr4:7542100..7544094,2	K562	blood:
29	chr4:7539171..7539671-chr6:30709977..30710667,2	Hela-S3	cervix:
30	chr4:7524802..7527211-chr4:7527477..7529278,2	MCF-7	breast:
31	chr4:7516846..7519696-chr4:7521879..7524111,2	K562	blood:
32	chr4:7455060..7457538-chr4:7459563..7461357,2	K562	blood:
33	chr4:7516092..7517714-chr4:7519119..7521315,2	K562	blood:
34	chr4:7337216..7338143-chr4:7463851..7464757,3	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4274	chr4:7461818-7461835	MIMAT0016906

No data

Variant related genes	Relation type
MIR4274	TF binding region
MIR4274	CpG island
ENSG00000137804	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000013588	chromatin interactions

Extended variants
information (count: 5117 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:5117 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56404112	chr4:7456717-7456718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145515982	chr4:7456748-7456749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200442609	chr4:7456763-7456764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs71612272	chr4:7456868-7456869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs66637290	chr4:7456904-7456905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199957438	chr4:7456921-7456922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556044724	chr4:7456933-7456934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577488274	chr4:7456934-7456935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373567655	chr4:7456970-7456971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376811719	chr4:7456974-7456975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545089241	chr4:7457003-7457004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201613165	chr4:7457011-7457012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs71613818	chr4:7457031-7457032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200866163	chr4:7457048-7457049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560523908	chr4:7457049-7457050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200453939	chr4:7457122-7457123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538750040	chr4:7457136-7457137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386671225	chr4:7457137-7457138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572493275	chr4:7457139-7457140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543097912	chr4:7457140-7457141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373958638	chr4:7457153-7457154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556897168	chr4:7457173-7457174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561183679	chr4:7457175-7457176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180705905	chr4:7457186-7457187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369983865	chr4:7457194-7457195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565591123	chr4:7457204-7457205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376889193	chr4:7457217-7457218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532835683	chr4:7457241-7457242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71601841	chr4:7457248-7457249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184321086	chr4:7457268-7457269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566463176	chr4:7457299-7457300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533694026	chr4:7457307-7457308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549073867	chr4:7457324-7457325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569175432	chr4:7457326-7457327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200221125	chr4:7457331-7457332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566977955	chr4:7457361-7457362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537672581	chr4:7457362-7457363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555907557	chr4:7457363-7457364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577550564	chr4:7457367-7457368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188665357	chr4:7457372-7457373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553919155	chr4:7457376-7457377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368055024	chr4:7457399-7457400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572413863	chr4:7457403-7457404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182093526	chr4:7457406-7457407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561389063	chr4:7457427-7457428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542814548	chr4:7457434-7457435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs59865477	chr4:7457472-7457473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375630430	chr4:7457481-7457482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186697372	chr4:7457534-7457535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532901262	chr4:7457541-7457542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7437800-7462400	Weak transcription	Right Atrium	heart
2	chr4:7454400-7458200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:7455000-7460000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:7458200-7459400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:7458800-7459200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr4:7458800-7459200	Active TSS	Spleen	Spleen
7	chr4:7459000-7459400	Enhancers	Gastric	stomach
8	chr4:7459000-7463200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:7459200-7459400	Bivalent Enhancer	Lung	lung
10	chr4:7459200-7459600	Bivalent Enhancer	Fetal Stomach	stomach
11	chr4:7459400-7460000	Enhancers	Brain Germinal Matrix	brain
12	chr4:7459400-7460600	Bivalent Enhancer	Fetal Muscle Leg	muscle
13	chr4:7459400-7460800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr4:7459400-7462400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:7459600-7459800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
16	chr4:7459600-7459800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
17	chr4:7459800-7460400	Enhancers	Ovary	ovary
18	chr4:7460000-7462400	Weak transcription	Brain Germinal Matrix	brain
19	chr4:7460400-7460800	Weak transcription	Ovary	ovary
20	chr4:7460800-7466000	Enhancers	Ovary	ovary
21	chr4:7461000-7466000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr4:7461400-7462000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:7461800-7462600	Enhancers	Fetal Stomach	stomach
24	chr4:7461800-7463000	Enhancers	Fetal Muscle Leg	muscle
25	chr4:7462000-7462200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
26	chr4:7462000-7462400	Enhancers	HSMM	muscle
27	chr4:7462000-7462600	Enhancers	Psoas Muscle	Psoas
28	chr4:7462000-7464800	Enhancers	Stomach Smooth Muscle	stomach
29	chr4:7462000-7465400	Enhancers	Brain Substantia Nigra	brain
30	chr4:7462000-7465600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:7462200-7462400	Bivalent Enhancer	Adipose Nuclei	Adipose
32	chr4:7462200-7462400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr4:7462200-7462400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
34	chr4:7462200-7462600	Enhancers	Liver	Liver
35	chr4:7462200-7462600	Enhancers	Fetal Kidney	kidney
36	chr4:7462200-7462600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
37	chr4:7462200-7462800	Bivalent Enhancer	Placenta	Placenta
38	chr4:7462200-7462800	Enhancers	HSMMtube	muscle
39	chr4:7462200-7463000	Bivalent Enhancer	HepG2	liver
40	chr4:7462200-7464000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr4:7462200-7464400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:7462200-7464800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:7462200-7464800	Enhancers	Fetal Intestine Small	intestine
44	chr4:7462200-7465800	Enhancers	Brain Cingulate Gyrus	brain
45	chr4:7462200-7466000	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr4:7462400-7462600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:7462400-7462600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:7462400-7462600	Enhancers	Adipose Nuclei	Adipose
49	chr4:7462400-7462800	Bivalent Enhancer	HSMM	muscle
50	chr4:7462400-7463400	Enhancers	Brain Germinal Matrix	brain

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