Variant report

Variant	nsv482087
Chromosome Location	chr4:9783258-9785633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:427)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:9784048-9784153	H1-hESC	embryonic stem cell:	n/a	n/a
2	FOSL2	chr4:9784693-9785308	HepG2	liver:	n/a	n/a
3	GABPA	chr4:9783175-9783540	H1-hESC	embryonic stem cell:	n/a	chr4:9783489-9783498
4	GATA3	chr4:9784087-9784539	MCF-7	breast:	n/a	n/a
5	JUND	chr4:9783811-9784008	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAFK	chr4:9783940-9783948	HepG2	liver:	n/a	n/a
7	POLR2A	chr4:9784665-9784823	A549	lung:	n/a	n/a
8	POLR2A	chr4:9784798-9784809	Gliobla	brain:	n/a	n/a
9	POLR2A	chr4:9784838-9784854	HepG2	liver:	n/a	n/a
10	POLR2A	chr4:9784036-9784078	HepG2	liver:	n/a	n/a
11	RAD21	chr4:9783766-9783842	H1-hESC	embryonic stem cell:	n/a	n/a
12	RFX5	chr4:9783426-9783428	HepG2	liver:	n/a	n/a
13	SIN3A	chr4:9783001-9783554	H1-hESC	embryonic stem cell:	n/a	chr4:9783495-9783506 chr4:9783236-9783249
14	TBP	chr4:9782917-9783541	H1-hESC	embryonic stem cell:	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	chr4:9783246-9783296	HMEC	breast:	n/a
2	chr4:9784508-9784558	A549	lung:	n/a
3	chr4:9783246-9783296	Hepatocyte	liver:	n/a
4	chr4:9783246-9783296	ECC-1	luminal epithelium:	n/a
5	chr4:9783953-9784003	ovcar-3	ovarian:	n/a
6	chr4:9783623-9783673	NB4	blood:	n/a
7	chr4:9783398-9783448	U87	brain:	n/a
8	chr4:9784508-9784558	CMK	blood:	n/a
9	chr4:9783363-9783413	GM12891	blood:	n/a
10	chr4:9783623-9783673	HAEpiC	amniotic membrane:	n/a
11	chr4:9783246-9783296	SAEC	small airway:	n/a
12	chr4:9783363-9783413	BE2_C	brain:	n/a
13	chr4:9783363-9783413	PANC-1	pancreas:	n/a
14	chr4:9783246-9783296	BE2_C	brain:	n/a
15	chr4:9784508-9784558	AG09309	skin:	n/a
16	chr4:9783623-9783673	ProgFib	skin:	n/a
17	chr4:9783363-9783413	PFSK-1	brain:	n/a
18	chr4:9783398-9783448	SKMC	muscle:	n/a
19	chr4:9783953-9784003	Hepatocyte	liver:	n/a
20	chr4:9783953-9784003	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:9783953-9784003	HCF	heart:	n/a
22	chr4:9784508-9784558	NH-A	brain:	n/a
23	chr4:9783965-9784015	HMEC	breast:	n/a
24	chr4:9784508-9784558	HEK293	kidney:	embryo
25	chr4:9783965-9784015	IMR90	lung:	fetal
26	chr4:9783398-9783448	HNPCEpiC	eye:	n/a
27	chr4:9783953-9784003	AG09319	gingival:	n/a
28	chr4:9784508-9784558	GM12878	blood:	n/a
29	chr4:9783398-9783448	HRCEpiC	kidney:	n/a
30	chr4:9783246-9783296	HPAEpiC	pulmonary alveolar:	n/a
31	chr4:9784508-9784558	ProgFib	skin:	n/a
32	chr4:9783398-9783448	NHDF-neo	bronchial:	n/a
33	chr4:9783965-9784015	AG09309	skin:	n/a
34	chr4:9783965-9784015	BE2_C	brain:	n/a
35	chr4:9783398-9783448	PANC-1	pancreas:	n/a
36	chr4:9783953-9784003	Hela-S3	cervix:	n/a
37	chr4:9783398-9783448	ovcar-3	ovarian:	n/a
38	chr4:9783965-9784015	Caco-2	colon:	n/a
39	chr4:9783246-9783296	NH-A	brain:	n/a
40	chr4:9783965-9784015	ovcar-3	ovarian:	n/a
41	chr4:9783965-9784015	SKMC	muscle:	n/a
42	chr4:9784508-9784558	SK-N-MC	brain:	n/a
43	chr4:9783246-9783296	A549	lung:	n/a
44	chr4:9783623-9783673	HCF	heart:	n/a
45	chr4:9783953-9784003	NH-A	brain:	n/a
46	chr4:9784508-9784558	Hela-S3	cervix:	n/a
47	chr4:9783623-9783673	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:9784508-9784558	HCM	heart:	n/a
49	chr4:9783398-9783448	HCM	heart:	n/a
50	chr4:9783953-9784003	A549	lung:	n/a

No data

Variant related genes	Relation type
DRD5	TF binding region
DRD5	CpG island

Extended variants
information (count: 143 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550305570	chr4:9783259-9783260	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs571812427	chr4:9783268-9783269	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs12504432	chr4:9783297-9783298	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs539022301	chr4:9783300-9783301	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs547504779	chr4:9783310-9783311	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs533889618	chr4:9783323-9783324	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs373637865	chr4:9783328-9783329	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs536560116	chr4:9783412-9783413	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs554715522	chr4:9783421-9783422	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs2076907	chr4:9783428-9783429	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs371572831	chr4:9783442-9783443	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs375251229	chr4:9783485-9783486	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs537286412	chr4:9783494-9783495	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs558226166	chr4:9783527-9783528	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs576892102	chr4:9783528-9783529	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs372681931	chr4:9783559-9783560	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs559099689	chr4:9783604-9783605	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs368710755	chr4:9783622-9783623	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs542146372	chr4:9783633-9783634	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs563430281	chr4:9783648-9783649	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs200812406	chr4:9783649-9783650	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs368348754	chr4:9783650-9783651	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs565360620	chr4:9783680-9783681	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs371107353	chr4:9783705-9783706	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs191825696	chr4:9783719-9783720	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs565962667	chr4:9783749-9783750	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs567268264	chr4:9783753-9783754	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs201330876	chr4:9783775-9783776	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs536904632	chr4:9783782-9783783	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs144460797	chr4:9783792-9783793	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs201926104	chr4:9783802-9783803	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs199687249	chr4:9783815-9783816	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs2227839	chr4:9783816-9783817	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs145405809	chr4:9783818-9783819	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs377175551	chr4:9783828-9783829	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs113223975	chr4:9783834-9783835	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs2227840	chr4:9783838-9783839	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs570059380	chr4:9783839-9783840	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs201023282	chr4:9783875-9783876	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs151282040	chr4:9783877-9783878	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs2227848	chr4:9783905-9783906	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs148402761	chr4:9783915-9783916	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs6282	chr4:9783916-9783917	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs76288744	chr4:9783917-9783918	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs147038465	chr4:9783954-9783955	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs147655139	chr4:9783969-9783970	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs113695344	chr4:9783971-9783972	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs534438513	chr4:9783976-9783977	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs184288806	chr4:9783977-9783978	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs2227849	chr4:9783982-9783983	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
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
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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9782400-9783400	Bivalent Enhancer	Fetal Muscle Leg	muscle
2	chr4:9782600-9783800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
3	chr4:9782600-9784000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr4:9782800-9783400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:9782800-9783400	Active TSS	Colonic Mucosa	Colon
6	chr4:9782800-9783400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr4:9782800-9783600	Active TSS	H9 Cell Line	embryonic stem cell
8	chr4:9782800-9783600	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:9782800-9783800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
10	chr4:9782800-9783800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
11	chr4:9782800-9783800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
12	chr4:9782800-9784000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
13	chr4:9782800-9784000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
14	chr4:9782800-9784000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
15	chr4:9783000-9783400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:9783000-9783400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
17	chr4:9783000-9783600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr4:9783000-9783600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:9783000-9783600	Bivalent/Poised TSS	Fetal Brain Female	brain
20	chr4:9783000-9783600	Active TSS	Right Atrium	heart
21	chr4:9783000-9783800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:9783000-9783800	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:9783000-9783800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:9783000-9784000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:9783000-9784000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
26	chr4:9783000-9784000	Bivalent Enhancer	Fetal Brain Male	brain
27	chr4:9783200-9783400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
28	chr4:9783200-9783400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
29	chr4:9783200-9783600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:9783200-9783600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:9783200-9783600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
32	chr4:9783200-9783600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr4:9783200-9783600	Bivalent Enhancer	Left Ventricle	heart
34	chr4:9783200-9783600	Flanking Bivalent TSS/Enh	Right Ventricle	heart
35	chr4:9783200-9783600	Bivalent Enhancer	HMEC	breast
36	chr4:9783400-9783600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
37	chr4:9783400-9783600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:9783400-9783600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr4:9783400-9783600	Bivalent/Poised TSS	Colonic Mucosa	Colon
40	chr4:9783400-9783600	Bivalent Enhancer	Fetal Intestine Small	intestine
41	chr4:9783400-9783600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
42	chr4:9783400-9783600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
43	chr4:9783400-9783800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:9783400-9783800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr4:9783400-9783800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
46	chr4:9783400-9784200	Bivalent Enhancer	Esophagus	oesophagus
47	chr4:9783600-9783800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:9783600-9783800	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
49	chr4:9783600-9783800	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
50	chr4:9783600-9783800	Bivalent Enhancer	Fetal Muscle Leg	muscle

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