Variant report

Variant	esv3416677
Chromosome Location	chr4:1399202-1401400
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:23)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

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

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1399938-1399988	SK-N-SH_RA	brain:	n/a
2	chr4:1400869-1400919	SKMC	muscle:	n/a
3	chr4:1399938-1399988	GM12892	blood:	n/a
4	chr4:1400189-1400239	Caco-2	colon:	n/a
5	chr4:1399516-1399566	HL-60	blood:	n/a
6	chr4:1399516-1399566	HEK293	kidney:	embryo
7	chr4:1400869-1400919	RPTEC	kidney:	n/a
8	chr4:1399235-1399285	SK-N-SH	brain:	n/a
9	chr4:1399516-1399566	MCF10A-Er-Src	breast:	n/a
10	chr4:1399516-1399566	CMK	blood:	n/a
11	chr4:1400189-1400239	T-47D	breast:	n/a
12	chr4:1400189-1400239	ECC-1	luminal epithelium:	n/a
13	chr4:1399938-1399988	AG04449	skin:	fetal
14	chr4:1399516-1399566	HRE	kidney:	n/a
15	chr4:1399235-1399285	HRPEpiC	eye:	n/a
16	chr4:1399938-1399988	NT2-D1	testis:	n/a
17	chr4:1400869-1400919	HCT-116	colon:	n/a
18	chr4:1399235-1399285	HCF	heart:	n/a
19	chr4:1399235-1399285	HAEpiC	amniotic membrane:	n/a
20	chr4:1399938-1399988	HMEC	breast:	n/a
21	chr4:1399235-1399285	HCM	heart:	n/a
22	chr4:1399235-1399285	HIPEpiC	eye:	n/a
23	chr4:1400869-1400919	HepG2	liver:	n/a
24	chr4:1399938-1399988	HRE	kidney:	n/a
25	chr4:1399938-1399988	H1-hESC	embryonic stem cell:	embryo
26	chr4:1400869-1400919	HCPEpiC	choroid plexus:	n/a
27	chr4:1399235-1399285	HepG2	liver:	n/a
28	chr4:1400189-1400239	HMEC	breast:	n/a
29	chr4:1399938-1399988	U87	brain:	n/a
30	chr4:1400189-1400239	GM12891	blood:	n/a
31	chr4:1400869-1400919	Caco-2	colon:	n/a
32	chr4:1400869-1400919	Hepatocyte	liver:	n/a
33	chr4:1400869-1400919	NT2-D1	testis:	n/a
34	chr4:1399235-1399285	NHDF-neo	bronchial:	n/a
35	chr4:1400189-1400239	NHDF-neo	bronchial:	n/a
36	chr4:1399938-1399988	SKMC	muscle:	n/a
37	chr4:1399516-1399566	AG04449	skin:	fetal
38	chr4:1400869-1400919	H1-hESC	embryonic stem cell:	embryo
39	chr4:1399938-1399988	CMK	blood:	n/a
40	chr4:1400189-1400239	HAEpiC	amniotic membrane:	n/a
41	chr4:1399235-1399285	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:1400189-1400239	AG09309	skin:	n/a
43	chr4:1399938-1399988	HEK293	kidney:	embryo
44	chr4:1399516-1399566	A549	lung:	n/a
45	chr4:1399235-1399285	Caco-2	colon:	n/a
46	chr4:1399938-1399988	PrEC	prostate:	n/a
47	chr4:1399516-1399566	AG09309	skin:	n/a
48	chr4:1399938-1399988	ECC-1	luminal epithelium:	n/a
49	chr4:1399938-1399988	MCF10A-Er-Src	breast:	n/a
50	chr4:1399516-1399566	HCT-116	colon:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1400709..1403410-chr4:1544391..1546329,2	K562	blood:
2	chr4:1393172..1395524-chr4:1397007..1399469,2	K562	blood:
3	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: 76 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:76 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73797207	chr4:1399205-1399206	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538136561	chr4:1399206-1399207	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369948703	chr4:1399208-1399209	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571935861	chr4:1399214-1399215	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184838390	chr4:1399227-1399228	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189348441	chr4:1399263-1399264	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372462142	chr4:1399294-1399295	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569640135	chr4:1399329-1399330	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537094882	chr4:1399330-1399331	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548678735	chr4:1399359-1399360	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111710573	chr4:1399406-1399407	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113289381	chr4:1399448-1399449	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536127570	chr4:1399450-1399451	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554410066	chr4:1399461-1399462	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572631826	chr4:1399462-1399463	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113357746	chr4:1399474-1399475	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558280133	chr4:1399512-1399513	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576439662	chr4:1399529-1399530	Bivalent Enhancer ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539034771	chr4:1399618-1399619	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113079298	chr4:1399628-1399629	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573617758	chr4:1399638-1399639	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557346479	chr4:1399655-1399656	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs13121529	chr4:1399780-1399781	Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	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
25	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
26	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
27	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
28	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
29	rs13122035	chr4:1400008-1400009	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530505865	chr4:1400031-1400032	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548979297	chr4:1400059-1400060	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111260457	chr4:1400069-1400070	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567224739	chr4:1400089-1400090	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529622988	chr4:1400149-1400150	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs548151088	chr4:1400152-1400153	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs566374962	chr4:1400158-1400159	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs72613115	chr4:1400172-1400173	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs558055050	chr4:1400185-1400186	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs570151861	chr4:1400213-1400214	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs80346978	chr4:1400313-1400314	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
41	rs144637631	chr4:1400340-1400341	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs538221182	chr4:1400430-1400431	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573655328	chr4:1400460-1400461	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs541015988	chr4:1400462-1400463	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs552894370	chr4:1400469-1400470	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs577837586	chr4:1400491-1400492	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs545221739	chr4:1400506-1400507	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs35911914	chr4:1400558-1400559	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs148476935	chr4:1400575-1400576	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112908403	chr4:1400589-1400590	Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	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:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1395800-1399400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr4:1396200-1400800	Enhancers	Pancreas	Pancrea
3	chr4:1396800-1402600	Bivalent Enhancer	Fetal Brain Male	brain
4	chr4:1397000-1399600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
5	chr4:1397200-1401000	Bivalent Enhancer	Brain Hippocampus Middle	brain
6	chr4:1397600-1401000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:1397600-1401200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:1397600-1402400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:1397800-1399400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
10	chr4:1398000-1399400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
11	chr4:1398000-1400600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:1398000-1401600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
13	chr4:1398600-1402600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:1398800-1399600	Bivalent Enhancer	Brain Germinal Matrix	brain
15	chr4:1398800-1401000	Bivalent Enhancer	Spleen	Spleen
16	chr4:1398800-1402400	Bivalent Enhancer	Right Ventricle	heart
17	chr4:1399000-1399600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
18	chr4:1399000-1402200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
19	chr4:1399200-1399800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:1399200-1399800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
21	chr4:1399400-1399600	Bivalent Enhancer	Fetal Intestine Small	intestine
22	chr4:1399400-1400400	Bivalent Enhancer	Esophagus	oesophagus
23	chr4:1399600-1399800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
24	chr4:1399600-1399800	Bivalent Enhancer	Colonic Mucosa	Colon
25	chr4:1399600-1399800	Bivalent Enhancer	Fetal Brain Female	brain
26	chr4:1399600-1400000	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
27	chr4:1399600-1401800	Bivalent Enhancer	Lung	lung
28	chr4:1399800-1400000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
29	chr4:1399800-1400400	Enhancers	Stomach Smooth Muscle	stomach
30	chr4:1399800-1400600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr4:1399800-1400800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
32	chr4:1399800-1401000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:1399800-1401400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr4:1399800-1401800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
35	chr4:1399800-1401800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
36	chr4:1399800-1402000	Bivalent/Poised TSS	Fetal Brain Female	brain
37	chr4:1399800-1411200	Weak transcription	Right Atrium	heart
38	chr4:1400000-1400200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
39	chr4:1400000-1400400	Bivalent Enhancer	Brain Cingulate Gyrus	brain
40	chr4:1400200-1400400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
41	chr4:1400200-1400400	Bivalent Enhancer	Ovary	ovary
42	chr4:1400200-1400600	Bivalent/Poised TSS	Psoas Muscle	Psoas
43	chr4:1400200-1401000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:1400200-1401000	Enhancers	Liver	Liver
45	chr4:1400200-1401200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr4:1400400-1400600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
47	chr4:1400400-1401200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr4:1400400-1401600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
49	chr4:1400400-1401800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
50	chr4:1400400-1403000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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