Variant report

Variant	esv1000883
Chromosome Location	chr5:180043250-180045421
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180044026-180044076	PFSK-1	brain:	n/a
2	chr5:180044026-180044076	HRPEpiC	eye:	n/a
3	chr5:180044026-180044076	NB4	blood:	n/a
4	chr5:180044026-180044076	HCT-116	colon:	n/a
5	chr5:180044026-180044076	ECC-1	luminal epithelium:	n/a
6	chr5:180044026-180044076	GM12892	blood:	n/a
7	chr5:180044026-180044076	Hela-S3	cervix:	n/a
8	chr5:180044026-180044076	AG04449	skin:	fetal
9	chr5:180044026-180044076	NT2-D1	testis:	n/a
10	chr5:180044026-180044076	ovcar-3	ovarian:	n/a
11	chr5:180044026-180044076	HAEpiC	amniotic membrane:	n/a
12	chr5:180044026-180044076	BJ	skin:	n/a
13	chr5:180044026-180044076	HRCEpiC	kidney:	n/a
14	chr5:180044026-180044076	HCPEpiC	choroid plexus:	n/a
15	chr5:180044026-180044076	HCM	heart:	n/a
16	chr5:180044026-180044076	Jurkat	blood:	n/a
17	chr5:180044026-180044076	HMEC	breast:	n/a
18	chr5:180044026-180044076	HRE	kidney:	n/a
19	chr5:180044026-180044076	AG04450	lung:	fetal
20	chr5:180044026-180044076	HEK293	kidney:	embryo
21	chr5:180044026-180044076	SAEC	small airway:	n/a
22	chr5:180044026-180044076	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:180044026-180044076	SK-N-SH_RA	brain:	n/a
24	chr5:180044026-180044076	PrEC	prostate:	n/a
25	chr5:180044026-180044076	HNPCEpiC	eye:	n/a
26	chr5:180044026-180044076	IMR90	lung:	fetal
27	chr5:180044026-180044076	HL-60	blood:	n/a
28	chr5:180044026-180044076	SK-N-SH	brain:	n/a
29	chr5:180044026-180044076	SK-N-MC	brain:	n/a
30	chr5:180044026-180044076	H1-hESC	embryonic stem cell:	embryo
31	chr5:180044026-180044076	LNCaP	prostate:	n/a
32	chr5:180044026-180044076	T-47D	breast:	n/a
33	chr5:180044026-180044076	RPTEC	kidney:	n/a
34	chr5:180044026-180044076	Hepatocyte	liver:	n/a
35	chr5:180044026-180044076	AG10803	skin:	n/a
36	chr5:180044026-180044076	GM06990	blood:	n/a
37	chr5:180044026-180044076	AG09309	skin:	n/a
38	chr5:180044026-180044076	K562	blood:	n/a
39	chr5:180044026-180044076	NHDF-neo	bronchial:	n/a
40	chr5:180044026-180044076	CMK	blood:	n/a
41	chr5:180044026-180044076	AoSMC	blood vessel:	n/a
42	chr5:180044026-180044076	MCF10A-Er-Src	breast:	n/a
43	chr5:180044026-180044076	GM12891	blood:	n/a
44	chr5:180044026-180044076	AG09319	gingival:	n/a
45	chr5:180044026-180044076	HEEpiC	esophagus:	n/a
46	chr5:180044026-180044076	U87	brain:	n/a
47	chr5:180044026-180044076	GM19239	blood:	n/a
48	chr5:180044026-180044076	A549	lung:	n/a
49	chr5:180044026-180044076	ProgFib	skin:	n/a
50	chr5:180044026-180044076	NHBE	bronchial:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:180031301..180033388-chr5:180043244..180045976,2	MCF-7	breast:
2	chr5:179758608..179760983-chr5:180044449..180046070,2	MCF-7	breast:

No data

Variant related genes	Relation type
FLT4	CpG island
ENSG00000131459	chromatin interactions

Extended variants
information (count: 148 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:148 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187119687	chr5:180043257-180043258	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs369626688	chr5:180043281-180043282	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs534451517	chr5:180043292-180043293	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs55657009	chr5:180043330-180043331	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs373196198	chr5:180043345-180043346	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs376130794	chr5:180043353-180043354	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs370856459	chr5:180043382-180043383	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs1130378	chr5:180043388-180043389	Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs140277328	chr5:180043415-180043416	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs373876329	chr5:180043438-180043439	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs56127961	chr5:180043439-180043440	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs56310180	chr5:180043441-180043442	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs573813758	chr5:180043442-180043443	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs543013937	chr5:180043448-180043449	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs546970544	chr5:180043451-180043452	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs121909651	chr5:180043455-180043456	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs121909650	chr5:180043464-180043465	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs121909653	chr5:180043482-180043483	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs112258507	chr5:180043498-180043499	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs200714115	chr5:180043499-180043500	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs573267535	chr5:180043507-180043508	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs375643645	chr5:180043513-180043514	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs377562122	chr5:180043525-180043526	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs56196251	chr5:180043530-180043531	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs113708130	chr5:180043538-180043539	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs189966991	chr5:180043619-180043620	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs565348694	chr5:180043643-180043644	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs145493041	chr5:180043644-180043645	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs140245458	chr5:180043649-180043650	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs75559244	chr5:180043688-180043689	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs79450271	chr5:180043689-180043690	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs182247208	chr5:180043717-180043718	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs3765095	chr5:180043731-180043732	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs577748565	chr5:180043733-180043734	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs372475977	chr5:180043736-180043737	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs547262285	chr5:180043845-180043846	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs374772609	chr5:180043846-180043847	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs565370442	chr5:180043849-180043850	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs56290422	chr5:180043864-180043865	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs187747507	chr5:180043872-180043873	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs561691396	chr5:180043887-180043888	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs56082504	chr5:180043904-180043905	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs56144912	chr5:180043927-180043928	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs56364366	chr5:180043931-180043932	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs149033942	chr5:180043973-180043974	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs551084116	chr5:180043978-180043979	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs371048569	chr5:180044000-180044001	Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs113793749	chr5:180044012-180044013	Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs367783370	chr5:180044016-180044017	Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs200097920	chr5:180044017-180044018	Weak transcription ZNF genes & repeats Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180018800-180045800	Weak transcription	Right Atrium	heart
2	chr5:180029400-180045600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:180035600-180043400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr5:180037400-180043400	Weak transcription	Right Ventricle	heart
5	chr5:180039600-180044000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:180040000-180061200	Weak transcription	Gastric	stomach
7	chr5:180041400-180044800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:180042200-180045400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:180042200-180045400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:180043000-180045800	Weak transcription	Liver	Liver
11	chr5:180043200-180043400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr5:180043200-180043600	Strong transcription	Adipose Nuclei	Adipose
13	chr5:180043200-180043800	Bivalent Enhancer	Placenta	Placenta
14	chr5:180043200-180044000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:180043200-180044000	ZNF genes & repeats	Lung	lung
16	chr5:180043200-180044000	ZNF genes & repeats	Spleen	Spleen
17	chr5:180043400-180043800	Enhancers	Brain Anterior Caudate	brain
18	chr5:180043400-180043800	Bivalent Enhancer	Right Ventricle	heart
19	chr5:180043400-180044000	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:180043400-180044000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr5:180043600-180044200	ZNF genes & repeats	Adipose Nuclei	Adipose
22	chr5:180043600-180044200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
23	chr5:180043800-180044000	Bivalent Enhancer	Brain Anterior Caudate	brain
24	chr5:180043800-180044000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr5:180044000-180044800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:180044000-180045400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:180044000-180045400	Weak transcription	Spleen	Spleen
28	chr5:180044000-180046000	Weak transcription	Lung	lung
29	chr5:180044800-180045400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:180044800-180046600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:180045400-180045600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:180045400-180045600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr5:180045400-180045600	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:180045400-180045600	Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr5:180045400-180045600	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr5:180045400-180045600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:180045400-180045600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr5:180045400-180045600	Bivalent Enhancer	Brain Germinal Matrix	brain
39	chr5:180045400-180045600	Enhancers	Esophagus	oesophagus
40	chr5:180045400-180045600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr5:180045400-180045600	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr5:180045400-180045600	Bivalent Enhancer	Placenta	Placenta
43	chr5:180045400-180045600	Bivalent Enhancer	Right Ventricle	heart
44	chr5:180045400-180045800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr5:180045400-180045800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr5:180045400-180045800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:180045400-180045800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr5:180045400-180045800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
49	chr5:180045400-180045800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
50	chr5:180045400-180046000	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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