Variant report

Variant	nsv597852
Chromosome Location	chr5:37839885-37840407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:367)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr5:37839864-37840661	HepG2	liver:	n/a	chr5:37839968-37839984 chr5:37839973-37839989 chr5:37839947-37839963
2	CHD2	chr5:37840379-37840789	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTBP2	chr5:37839040-37840731	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr5:37840400-37840749	ProgFib	skin:	n/a	n/a
5	CTCF	chr5:37839946-37840083	NHEK	skin:	n/a	n/a
6	CTCF	chr5:37839920-37840070	AG04449	skin:	n/a	n/a
7	CTCF	chr5:37839980-37840130	GM12865	blood:	n/a	n/a
8	CTCF	chr5:37840387-37840605	T-47D	breast:	n/a	n/a
9	CTCF	chr5:37840389-37840629	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr5:37840398-37840646	MCF-7	breast:	n/a	n/a
11	CTCF	chr5:37839940-37840090	AG09319	gingival:	n/a	n/a
12	CTCF	chr5:37839960-37840110	HCFaa	heart:	n/a	n/a
13	CTCF	chr5:37840300-37840450	HCM	heart:	n/a	n/a
14	CTCF	chr5:37840400-37840550	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr5:37840200-37840350	GM12865	blood:	n/a	n/a
16	CTCF	chr5:37839880-37840030	GM12865	blood:	n/a	n/a
17	CTCF	chr5:37840400-37840551	GM13977	blood:	n/a	n/a
18	CTCF	chr5:37839920-37840070	AG04450	lung:	n/a	n/a
19	CTCF	chr5:37839960-37840110	HEK293	kidney:	n/a	n/a
20	CTCF	chr5:37840400-37840550	Caco-2	colon:	n/a	n/a
21	CTCF	chr5:37840407-37840662	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:37840400-37840550	HEK293	kidney:	n/a	n/a
23	CTCF	chr5:37840330-37840854	IMR90	lung:	n/a	n/a
24	CTCF	chr5:37839968-37840045	MCF-7	breast:	n/a	n/a
25	CTCF	chr5:37840380-37840530	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr5:37839880-37840030	AG04450	lung:	n/a	n/a
27	CTCF	chr5:37839920-37840070	AG09319	gingival:	n/a	n/a
28	CTCF	chr5:37839980-37840130	HEK293	kidney:	n/a	n/a
29	CTCF	chr5:37839980-37840130	BJ	skin:	n/a	n/a
30	CTCF	chr5:37840000-37840150	HRE	kidney:	n/a	n/a
31	CTCF	chr5:37839960-37840110	HMEC	breast:	n/a	n/a
32	CTCF	chr5:37839902-37840074	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:37839920-37840070	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr5:37839880-37840030	GM12869	blood:	n/a	n/a
35	CTCF	chr5:37839941-37840070	MCF-7	breast:	n/a	n/a
36	CTCF	chr5:37840260-37840410	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr5:37840380-37840530	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr5:37839920-37840070	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr5:37840372-37840668	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:37840320-37840470	GM12871	blood:	n/a	n/a
41	CTCF	chr5:37840406-37840788	Fibrobl	skin:	n/a	n/a
42	CTCF	chr5:37839960-37840110	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr5:37840380-37840530	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr5:37839922-37840090	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:37839870-37840127	IMR90	lung:	n/a	n/a
46	CTCF	chr5:37839971-37840018	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr5:37839991-37840074	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr5:37839900-37840050	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr5:37839940-37840090	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr5:37840380-37840530	HL-60	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37839943-37839993	HCPEpiC	choroid plexus:	n/a
2	chr5:37839943-37839993	HCPEpiC	choroid plexus:	n/a
3	chr5:37839923-37839973	T-47D	breast:	n/a
4	chr5:37839918-37839968	GM12891	blood:	n/a
5	chr5:37839943-37839993	HNPCEpiC	eye:	n/a
6	chr5:37840089-37840139	HCPEpiC	choroid plexus:	n/a
7	chr5:37840158-37840208	SAEC	small airway:	n/a
8	chr5:37840075-37840125	GM06990	blood:	n/a
9	chr5:37840089-37840139	PANC-1	pancreas:	n/a
10	chr5:37840089-37840139	HAEpiC	amniotic membrane:	n/a
11	chr5:37840158-37840208	RPTEC	kidney:	n/a
12	chr5:37839943-37839993	AG04449	skin:	fetal
13	chr5:37840089-37840139	NB4	blood:	n/a
14	chr5:37839923-37839973	HL-60	blood:	n/a
15	chr5:37839943-37839993	AG09309	skin:	n/a
16	chr5:37839918-37839968	Caco-2	colon:	n/a
17	chr5:37840075-37840125	HAEpiC	amniotic membrane:	n/a
18	chr5:37839918-37839968	HMEC	breast:	n/a
19	chr5:37839918-37839968	U87	brain:	n/a
20	chr5:37840089-37840139	GM12891	blood:	n/a
21	chr5:37840089-37840139	ProgFib	skin:	n/a
22	chr5:37840075-37840125	SK-N-MC	brain:	n/a
23	chr5:37840075-37840125	HCF	heart:	n/a
24	chr5:37840089-37840139	RPTEC	kidney:	n/a
25	chr5:37840075-37840125	HIPEpiC	eye:	n/a
26	chr5:37840158-37840208	AG04450	lung:	fetal
27	chr5:37839943-37839993	PFSK-1	brain:	n/a
28	chr5:37840158-37840208	PFSK-1	brain:	n/a
29	chr5:37839923-37839973	ECC-1	luminal epithelium:	n/a
30	chr5:37839918-37839968	T-47D	breast:	n/a
31	chr5:37839943-37839993	A549	lung:	n/a
32	chr5:37839943-37839993	HRPEpiC	eye:	n/a
33	chr5:37840158-37840208	HRE	kidney:	n/a
34	chr5:37839943-37839993	T-47D	breast:	n/a
35	chr5:37840158-37840208	HMEC	breast:	n/a
36	chr5:37840075-37840125	NHDF-neo	bronchial:	n/a
37	chr5:37840075-37840125	AG09309	skin:	n/a
38	chr5:37839918-37839968	SK-N-MC	brain:	n/a
39	chr5:37839918-37839968	PFSK-1	brain:	n/a
40	chr5:37839918-37839968	GM12892	blood:	n/a
41	chr5:37839943-37839993	AoSMC	blood vessel:	n/a
42	chr5:37839918-37839968	SK-N-SH_RA	brain:	n/a
43	chr5:37839943-37839993	GM19239	blood:	n/a
44	chr5:37840075-37840125	HUVEC	blood vessel:	n/a
45	chr5:37840075-37840125	SKMC	muscle:	n/a
46	chr5:37839918-37839968	HL-60	blood:	n/a
47	chr5:37839923-37839973	SK-N-SH_RA	brain:	n/a
48	chr5:37839923-37839973	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:37840075-37840125	SK-N-SH_RA	brain:	n/a
50	chr5:37840089-37840139	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:37834038..37837439-chr5:37839505..37841588,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR70-1	chr5:37839970-37840675	NONHSAT101070

No data

Variant related genes	Relation type
GDNF	TF binding region
GDNF-AS1	TF binding region
GDNF	CpG island
GDNF-AS1	CpG island
ENSG00000168621	chromatin interactions

Extended variants
information (count: 19 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553127907	chr5:37839911-37839912	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs577983188	chr5:37839946-37839947	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs545689245	chr5:37839961-37839962	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs563976552	chr5:37839974-37839975	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs531089406	chr5:37839984-37839985	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs543286033	chr5:37840099-37840100	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs561743547	chr5:37840109-37840110	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs529011322	chr5:37840177-37840178	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs192595720	chr5:37840232-37840233	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs2075681	chr5:37840243-37840244	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs374694499	chr5:37840248-37840249	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs184461513	chr5:37840253-37840254	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs146787314	chr5:37840314-37840315	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs569654514	chr5:37840331-37840332	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs536843749	chr5:37840353-37840354	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs140465340	chr5:37840397-37840398	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs567733935	chr5:37840398-37840399	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs534774326	chr5:37840402-37840403	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs2735272	chr5:37840407-37840408	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19197363	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37834200-37841000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
2	chr5:37834400-37840600	Bivalent Enhancer	Fetal Brain Male	brain
3	chr5:37834400-37841400	Bivalent/Poised TSS	Colonic Mucosa	Colon
4	chr5:37835800-37840000	Bivalent Enhancer	Spleen	Spleen
5	chr5:37836200-37840200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr5:37836200-37840600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
7	chr5:37836200-37840800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
8	chr5:37836200-37840800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
9	chr5:37836200-37840800	Active TSS	NHDF-Ad	bronchial
10	chr5:37836200-37841000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
11	chr5:37836200-37841000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:37836400-37840600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr5:37836400-37840600	Active TSS	HSMM	muscle
14	chr5:37836400-37840800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
15	chr5:37836400-37841200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
16	chr5:37836400-37841600	Active TSS	HSMMtube	muscle
17	chr5:37836600-37840000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
18	chr5:37836600-37840000	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
19	chr5:37836600-37840200	Enhancers	Lung	lung
20	chr5:37836600-37841000	Flanking Active TSS	HMEC	breast
21	chr5:37837000-37840600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
22	chr5:37837000-37840800	Active TSS	Osteobl	bone
23	chr5:37838000-37841200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
24	chr5:37838200-37840000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
25	chr5:37838200-37841400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
26	chr5:37838400-37840800	Active TSS	Rectal Smooth Muscle	rectum
27	chr5:37838400-37841000	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr5:37838600-37840200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr5:37838600-37841000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:37838600-37841000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
31	chr5:37839000-37840000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:37839200-37840000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:37839200-37840000	Flanking Bivalent TSS/Enh	HepG2	liver
34	chr5:37839200-37840200	Flanking Bivalent TSS/Enh	Right Ventricle	heart
35	chr5:37839200-37840600	Bivalent/Poised TSS	Sigmoid Colon	Sigmoid Colon
36	chr5:37839200-37840800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
37	chr5:37839200-37840800	Active TSS	Colon Smooth Muscle	Colon
38	chr5:37839200-37841000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:37839400-37840000	Bivalent Enhancer	HUVEC	blood vessel
40	chr5:37839400-37840400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
41	chr5:37839400-37840400	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:37839400-37840600	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:37839400-37840600	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:37839400-37840600	Active TSS	Fetal Kidney	kidney
45	chr5:37839400-37840800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:37839400-37841000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr5:37839600-37840000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr5:37839600-37840000	Flanking Bivalent TSS/Enh	Placenta Amnion	Placenta Amnion
49	chr5:37839600-37840200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
50	chr5:37839600-37840200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain

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