Variant report

Variant	nsv878566
Chromosome Location	chr4:7456717-7529367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:500)
CpG islands
(count:2200)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	ATF3	chr4:7462396-7462591	K562	blood:	n/a	chr4:7462510-7462519
3	BACH1	chr4:7474386-7474403	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:7459110-7459520	H1-hESC	embryonic stem cell:	n/a	n/a
5	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
6	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
7	BHLHE40	chr4:7463215-7463337	K562	blood:	n/a	chr4:7463252-7463273 chr4:7463259-7463268
8	CCNT2	chr4:7505792-7505967	K562	blood:	n/a	n/a
9	CEBPB	chr4:7517192-7517635	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:7525842-7526080	A549	lung:	n/a	chr4:7525982-7525993
11	CEBPB	chr4:7517322-7517536	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:7462372-7462637	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:7525826-7526412	HepG2	liver:	n/a	chr4:7525982-7525993
14	CEBPB	chr4:7517279-7517633	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:7517278-7517645	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:7517417-7517597	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:7525887-7526098	H1-hESC	embryonic stem cell:	n/a	chr4:7525982-7525993
18	CEBPB	chr4:7472785-7473103	MCF-7	breast:	n/a	n/a
19	CEBPB	chr4:7525934-7526014	IMR90	lung:	n/a	chr4:7525982-7525993
20	CEBPD	chr4:7517347-7517719	HepG2	liver:	n/a	n/a
21	CEBPD	chr4:7516506-7516755	HepG2	liver:	n/a	n/a
22	CHD2	chr4:7525404-7525516	HepG2	liver:	n/a	n/a
23	CHD2	chr4:7464210-7464433	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr4:7517348-7517609	HepG2	liver:	n/a	n/a
25	CREB1	chr4:7512161-7512419	A549	lung:	n/a	n/a
26	CTBP2	chr4:7465845-7466283	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:7464520-7464670	BJ	skin:	n/a	n/a
28	CTCF	chr4:7464500-7464650	K562	blood:	n/a	n/a
29	CTCF	chr4:7528248-7528482	K562	blood:	n/a	n/a
30	CTCF	chr4:7462440-7462590	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr4:7474240-7474390	HBMEC	blood vessel:	n/a	chr4:7474321-7474334
32	CTCF	chr4:7528320-7528470	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr4:7462460-7462610	AG04449	skin:	n/a	n/a
34	CTCF	chr4:7528360-7528510	BE2_C	brain:	n/a	n/a
35	CTCF	chr4:7462960-7463110	K562	blood:	n/a	chr4:7463085-7463094
36	CTCF	chr4:7464440-7464590	AG09309	skin:	n/a	n/a
37	CTCF	chr4:7528240-7528390	K562	blood:	n/a	n/a
38	CTCF	chr4:7469389-7469494	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr4:7464238-7464454	A549	lung:	n/a	n/a
40	CTCF	chr4:7474260-7474410	WERI-Rb-1	eye:	n/a	chr4:7474321-7474334
41	CTCF	chr4:7464500-7464650	AG10803	skin:	n/a	n/a
42	CTCF	chr4:7464240-7464442	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr4:7463020-7463170	HAc	cerebellar:	n/a	chr4:7463085-7463094
44	CTCF	chr4:7464275-7464704	K562	blood:	n/a	n/a
45	CTCF	chr4:7464307-7464371	GM19238	blood:	n/a	n/a
46	CTCF	chr4:7476207-7476287	MCF-7	breast:	n/a	chr4:7476252-7476261 chr4:7476252-7476265 chr4:7476249-7476267
47	CTCF	chr4:7464267-7464433	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:7464240-7464390	HEK293	kidney:	n/a	n/a
49	CTCF	chr4:7463040-7463190	Caco-2	colon:	n/a	chr4:7463085-7463094
50	CTCF	chr4:7464169-7464604	MCF-7	breast:	n/a	n/a

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7486195-7486245	HMEC	breast:	n/a
2	chr4:7473297-7473347	CMK	blood:	n/a
3	chr4:7479912-7479962	T-47D	breast:	n/a
4	chr4:7518360-7518410	HCPEpiC	choroid plexus:	n/a
5	chr4:7486195-7486245	HMEC	breast:	n/a
6	chr4:7473297-7473347	CMK	blood:	n/a
7	chr4:7479912-7479962	T-47D	breast:	n/a
8	chr4:7518360-7518410	HCPEpiC	choroid plexus:	n/a
9	chr4:7528296-7528346	NT2-D1	testis:	n/a
10	chr4:7512177-7512227	BE2_C	brain:	n/a
11	chr4:7502429-7502479	CMK	blood:	n/a
12	chr4:7512425-7512475	HL-60	blood:	n/a
13	chr4:7484382-7484432	SK-N-SH_RA	brain:	n/a
14	chr4:7502947-7502997	U87	brain:	n/a
15	chr4:7463234-7463284	Caco-2	colon:	n/a
16	chr4:7483577-7483627	SK-N-MC	brain:	n/a
17	chr4:7512278-7512328	SAEC	small airway:	n/a
18	chr4:7502947-7502997	HEK293	kidney:	embryo
19	chr4:7512016-7512066	ovcar-3	ovarian:	n/a
20	chr4:7462468-7462518	HEEpiC	esophagus:	n/a
21	chr4:7512425-7512475	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:7462664-7462714	HUVEC	blood vessel:	n/a
23	chr4:7463007-7463057	ProgFib	skin:	n/a
24	chr4:7462594-7462644	HEEpiC	esophagus:	n/a
25	chr4:7473297-7473347	U87	brain:	n/a
26	chr4:7512425-7512475	GM06990	blood:	n/a
27	chr4:7512278-7512328	AG04450	lung:	fetal
28	chr4:7502429-7502479	BE2_C	brain:	n/a
29	chr4:7502706-7502756	NH-A	brain:	n/a
30	chr4:7502947-7502997	HCPEpiC	choroid plexus:	n/a
31	chr4:7486195-7486245	GM12891	blood:	n/a
32	chr4:7528296-7528346	PANC-1	pancreas:	n/a
33	chr4:7512016-7512066	AG09319	gingival:	n/a
34	chr4:7528947-7528997	HIPEpiC	eye:	n/a
35	chr4:7518360-7518410	NHBE	bronchial:	n/a
36	chr4:7502429-7502479	HAEpiC	amniotic membrane:	n/a
37	chr4:7528129-7528179	Hepatocyte	liver:	n/a
38	chr4:7515958-7516008	SK-N-SH_RA	brain:	n/a
39	chr4:7462664-7462714	HCM	heart:	n/a
40	chr4:7512016-7512066	BE2_C	brain:	n/a
41	chr4:7518360-7518410	HRPEpiC	eye:	n/a
42	chr4:7502706-7502756	SKMC	muscle:	n/a
43	chr4:7511100-7511150	U87	brain:	n/a
44	chr4:7526521-7526571	A549	lung:	n/a
45	chr4:7528296-7528346	HCPEpiC	choroid plexus:	n/a
46	chr4:7528129-7528179	AG04449	skin:	fetal
47	chr4:7486195-7486245	BE2_C	brain:	n/a
48	chr4:7472958-7473008	SK-N-SH_RA	brain:	n/a
49	chr4:7518360-7518410	GM12892	blood:	n/a
50	chr4:7528947-7528997	SAEC	small airway:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7520525..7523407-chr4:7542100..7544094,2	K562	blood:
2	chr4:7444681..7447159-chr4:7457852..7459823,2	MCF-7	breast:
3	chr4:7524845..7525381-chr4:7721481..7722229,2	K562	blood:
4	chr4:7512552..7515805-chr4:7517576..7521782,4	MCF-7	breast:
5	chr4:7455060..7457538-chr4:7459563..7461357,2	K562	blood:
6	chr4:7516846..7519696-chr4:7521879..7524111,2	K562	blood:
7	chr4:7337216..7338143-chr4:7463851..7464757,3	MCF-7	breast:
8	chr4:7455060..7457538-chr4:7459563..7461357,2	K562	blood:
9	chr4:7509518..7511220-chr4:7514824..7517339,2	K562	blood:
10	chr4:7452936..7455745-chr4:7457448..7459365,2	MCF-7	breast:
11	chr4:7516846..7519696-chr4:7521879..7524111,2	K562	blood:
12	chr4:7396272..7396793-chr4:7463896..7464564,2	MCF-7	breast:
13	chr4:7516092..7517714-chr4:7519119..7521315,2	K562	blood:
14	chr4:7475842..7476773-chr4:7652108..7653034,2	MCF-7	breast:
15	chr4:7512552..7515805-chr4:7517576..7521782,4	MCF-7	breast:
16	chr4:7474972..7476940-chr4:7478120..7479939,2	MCF-7	breast:
17	chr4:7464162..7464863-chr4:7721037..7721847,3	MCF-7	breast:
18	chr4:7474972..7476940-chr4:7478120..7479939,2	MCF-7	breast:
19	chr4:7513451..7515620-chr4:7531524..7533326,2	K562	blood:
20	chr4:7516092..7517714-chr4:7519119..7521315,2	K562	blood:
21	chr4:7524802..7527211-chr4:7527477..7529278,2	MCF-7	breast:
22	chr4:7509518..7511220-chr4:7514824..7517339,2	K562	blood:
23	chr4:7524802..7527211-chr4:7527477..7529278,2	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

Extended variants
information (count: 4272 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:4272 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

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:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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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