Variant report

Variant	esv3395594
Chromosome Location	chr4:1398577-1401325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:26)
CpG islands
(count:488)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:1400460-1400505	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:1400954-1401084	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr4:1399593-1399806	K562	blood:	n/a	n/a
4	CTCF	chr4:1399906-1399969	Fibrobl	skin:	n/a	n/a
5	CTCF	chr4:1399854-1399974	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:1399900-1400050	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr4:1399840-1399990	HEK293	kidney:	n/a	n/a
8	CTCF	chr4:1400580-1400730	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr4:1399840-1399990	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr4:1399902-1400002	NHEK	skin:	n/a	n/a
11	CTCF	chr4:1399920-1399987	A549	lung:	n/a	n/a
12	CTCF	chr4:1401200-1401350	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr4:1399840-1399990	AG04449	skin:	n/a	n/a
14	ELF1	chr4:1398771-1398980	K562	blood:	n/a	chr4:1398959-1398971
15	GABPA	chr4:1401263-1401756	H1-hESC	embryonic stem cell:	n/a	n/a
16	GABPA	chr4:1398585-1399181	H1-hESC	embryonic stem cell:	n/a	chr4:1398921-1398935
17	GABPA	chr4:1399378-1401064	H1-hESC	embryonic stem cell:	n/a	chr4:1400316-1400325 chr4:1399417-1399426
18	GABPA	chr4:1398552-1399041	H1-hESC	embryonic stem cell:	n/a	chr4:1398921-1398935
19	GABPA	chr4:1401300-1401651	H1-hESC	embryonic stem cell:	n/a	n/a
20	GABPA	chr4:1399273-1401002	H1-hESC	embryonic stem cell:	n/a	chr4:1400316-1400325 chr4:1399417-1399426
21	MYC	chr4:1400358-1400444	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr4:1400299-1400842	H1-neurons	neurons:	n/a	n/a
23	POLR2A	chr4:1400409-1400772	H1-neurons	neurons:	n/a	n/a
24	REST	chr4:1400672-1400842	H1-hESC	embryonic stem cell:	n/a	n/a
25	SUZ12	chr4:1395488-1403017	NT2-D1	testis:	n/a	n/a
26	SUZ12	chr4:1398211-1400317	H1-hESC	embryonic stem cell:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1399235-1399285	AG09319	gingival:	n/a
2	chr4:1399938-1399988	AoSMC	blood vessel:	n/a
3	chr4:1400189-1400239	AG09319	gingival:	n/a
4	chr4:1399938-1399988	AG04450	lung:	fetal
5	chr4:1399938-1399988	HepG2	liver:	n/a
6	chr4:1399938-1399988	IMR90	lung:	fetal
7	chr4:1398798-1398848	NT2-D1	testis:	n/a
8	chr4:1399938-1399988	H1-hESC	embryonic stem cell:	embryo
9	chr4:1399235-1399285	ProgFib	skin:	n/a
10	chr4:1399135-1399185	Jurkat	blood:	n/a
11	chr4:1399516-1399566	NHBE	bronchial:	n/a
12	chr4:1400869-1400919	HUVEC	blood vessel:	n/a
13	chr4:1398599-1398649	RPTEC	kidney:	n/a
14	chr4:1399135-1399185	HRCEpiC	kidney:	n/a
15	chr4:1400869-1400919	MCF-7	breast:	n/a
16	chr4:1399516-1399566	GM12892	blood:	n/a
17	chr4:1398599-1398649	SK-N-SH	brain:	n/a
18	chr4:1399235-1399285	Caco-2	colon:	n/a
19	chr4:1399938-1399988	SAEC	small airway:	n/a
20	chr4:1399516-1399566	IMR90	lung:	fetal
21	chr4:1399135-1399185	PrEC	prostate:	n/a
22	chr4:1399235-1399285	SK-N-SH	brain:	n/a
23	chr4:1399135-1399185	SAEC	small airway:	n/a
24	chr4:1399235-1399285	SK-N-SH_RA	brain:	n/a
25	chr4:1400189-1400239	K562	blood:	n/a
26	chr4:1399235-1399285	HepG2	liver:	n/a
27	chr4:1398599-1398649	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:1399135-1399185	Caco-2	colon:	n/a
29	chr4:1398798-1398848	HRE	kidney:	n/a
30	chr4:1400869-1400919	HRCEpiC	kidney:	n/a
31	chr4:1400869-1400919	SK-N-MC	brain:	n/a
32	chr4:1400189-1400239	GM19239	blood:	n/a
33	chr4:1399938-1399988	SK-N-SH_RA	brain:	n/a
34	chr4:1399938-1399988	GM12878	blood:	n/a
35	chr4:1398798-1398848	AG10803	skin:	n/a
36	chr4:1399135-1399185	AG10803	skin:	n/a
37	chr4:1399938-1399988	NT2-D1	testis:	n/a
38	chr4:1398798-1398848	HRPEpiC	eye:	n/a
39	chr4:1398798-1398848	K562	blood:	n/a
40	chr4:1400869-1400919	HRPEpiC	eye:	n/a
41	chr4:1399516-1399566	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:1399235-1399285	GM12891	blood:	n/a
43	chr4:1399135-1399185	PFSK-1	brain:	n/a
44	chr4:1400189-1400239	Hepatocyte	liver:	n/a
45	chr4:1399516-1399566	AG09319	gingival:	n/a
46	chr4:1398599-1398649	MCF-7	breast:	n/a
47	chr4:1399135-1399185	HepG2	liver:	n/a
48	chr4:1400869-1400919	LNCaP	prostate:	n/a
49	chr4:1398798-1398848	AG04450	lung:	fetal
50	chr4:1400869-1400919	AG10803	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1393172..1395524-chr4:1397007..1399469,2	K562	blood:
2	chr4:1400709..1403410-chr4:1544391..1546329,2	K562	blood:
3	chr4:1397408..1399062-chr4:1402095..1403760,2	K562	blood:
4	chr4:1391809..1396481-chr4:1400263..1404304,5	K562	blood:

No data

Variant related genes	Relation type
NKX1-1	TF binding region
NKX1-1	CpG island

Extended variants
information (count: 97 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192128887	chr4:1398589-1398590	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372208022	chr4:1398597-1398598	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183206193	chr4:1398703-1398704	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565475520	chr4:1398722-1398723	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376437706	chr4:1398770-1398771	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539109128	chr4:1398780-1398781	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551110205	chr4:1398813-1398814	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187533226	chr4:1398832-1398833	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376169664	chr4:1398836-1398837	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538163433	chr4:1398850-1398851	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556854760	chr4:1398888-1398889	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575206501	chr4:1398893-1398894	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11731672	chr4:1398897-1398898	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs554391400	chr4:1398905-1398906	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572594203	chr4:1398906-1398907	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374512947	chr4:1398980-1398981	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546232535	chr4:1398992-1398993	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192833730	chr4:1399002-1399003	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372519320	chr4:1399051-1399052	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576425686	chr4:1399081-1399082	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543451878	chr4:1399094-1399095	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375762856	chr4:1399138-1399139	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73797207	chr4:1399205-1399206	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538136561	chr4:1399206-1399207	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369948703	chr4:1399208-1399209	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571935861	chr4:1399214-1399215	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184838390	chr4:1399227-1399228	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189348441	chr4:1399263-1399264	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372462142	chr4:1399294-1399295	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569640135	chr4:1399329-1399330	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537094882	chr4:1399330-1399331	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548678735	chr4:1399359-1399360	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111710573	chr4:1399406-1399407	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113289381	chr4:1399448-1399449	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536127570	chr4:1399450-1399451	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554410066	chr4:1399461-1399462	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572631826	chr4:1399462-1399463	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113357746	chr4:1399474-1399475	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558280133	chr4:1399512-1399513	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576439662	chr4:1399529-1399530	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539034771	chr4:1399618-1399619	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113079298	chr4:1399628-1399629	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573617758	chr4:1399638-1399639	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557346479	chr4:1399655-1399656	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13121529	chr4:1399780-1399781	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559129939	chr4:1399808-1399809	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532998243	chr4:1399871-1399872	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551282118	chr4:1399883-1399884	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141872547	chr4:1399897-1399898	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13120467	chr4:1400007-1400008	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
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
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1395800-1399200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr4:1395800-1399400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr4:1396200-1400800	Enhancers	Pancreas	Pancrea
4	chr4:1396800-1402600	Bivalent Enhancer	Fetal Brain Male	brain
5	chr4:1397000-1399600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
6	chr4:1397200-1399200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr4:1397200-1401000	Bivalent Enhancer	Brain Hippocampus Middle	brain
8	chr4:1397400-1399200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:1397600-1399000	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr4:1397600-1401000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr4:1397600-1401200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:1397600-1402400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:1397800-1398800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chr4:1397800-1399200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
15	chr4:1397800-1399400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
16	chr4:1398000-1398800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
17	chr4:1398000-1399400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
18	chr4:1398000-1400600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr4:1398000-1401600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
20	chr4:1398200-1398600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:1398400-1398600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:1398400-1398600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
23	chr4:1398400-1398800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
24	chr4:1398400-1399200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:1398600-1398800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:1398600-1398800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:1398600-1398800	Bivalent Enhancer	Fetal Intestine Large	intestine
28	chr4:1398600-1398800	Enhancers	Gastric	stomach
29	chr4:1398600-1398800	Bivalent Enhancer	Lung	lung
30	chr4:1398600-1398800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
31	chr4:1398600-1399000	Bivalent Enhancer	Ovary	ovary
32	chr4:1398600-1399200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
33	chr4:1398600-1399200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
34	chr4:1398600-1402600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:1398800-1399000	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
36	chr4:1398800-1399000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr4:1398800-1399200	Bivalent Enhancer	Esophagus	oesophagus
38	chr4:1398800-1399200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
39	chr4:1398800-1399600	Bivalent Enhancer	Brain Germinal Matrix	brain
40	chr4:1398800-1401000	Bivalent Enhancer	Spleen	Spleen
41	chr4:1398800-1402400	Bivalent Enhancer	Right Ventricle	heart
42	chr4:1399000-1399200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
43	chr4:1399000-1399200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
44	chr4:1399000-1399600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
45	chr4:1399000-1402200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
46	chr4:1399200-1399800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:1399200-1399800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
48	chr4:1399400-1399600	Bivalent Enhancer	Fetal Intestine Small	intestine
49	chr4:1399400-1400400	Bivalent Enhancer	Esophagus	oesophagus
50	chr4:1399600-1399800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell

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