Variant report

Variant	rs7712899
Chromosome Location	chr5:92908786-92908787
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:28)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:28 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr5:92907188-92909449	H1-neurons	neurons:	n/a	n/a
2	ZNF143	chr5:92908521-92909150	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAX	chr5:92908453-92909046	H1-hESC	embryonic stem cell:	n/a	chr5:92908748-92908758
4	CHD2	chr5:92908613-92908813	H1-hESC	embryonic stem cell:	n/a	n/a
5	NRF1	chr5:92908569-92908815	H1-hESC	embryonic stem cell:	n/a	chr5:92908700-92908714
6	E2F6	chr5:92908477-92908888	H1-hESC	embryonic stem cell:	n/a	chr5:92908599-92908608
7	USF2	chr5:92908608-92909104	H1-hESC	embryonic stem cell:	n/a	n/a
8	MXI1	chr5:92908740-92908940	H1-hESC	embryonic stem cell:	n/a	n/a
9	TCF12	chr5:92908672-92909188	H1-hESC	embryonic stem cell:	n/a	n/a
10	TEAD4	chr5:92908582-92909060	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:92908680-92909056	H1-hESC	embryonic stem cell:	n/a	n/a
12	SIN3A	chr5:92907492-92909005	H1-hESC	embryonic stem cell:	n/a	chr5:92907943-92907952
13	TCF12	chr5:92908481-92908928	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr5:92907604-92910294	H1-hESC	embryonic stem cell:	n/a	n/a
15	RAD21	chr5:92908491-92909039	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr5:92908558-92908879	H1-hESC	embryonic stem cell:	n/a	n/a
17	YY1	chr5:92908493-92909037	H1-hESC	embryonic stem cell:	n/a	chr5:92908596-92908610 chr5:92908596-92908607 chr5:92908593-92908607
18	SUZ12	chr5:92906886-92910078	H1-hESC	embryonic stem cell:	n/a	n/a
19	RAD21	chr5:92908122-92908910	H1-hESC	embryonic stem cell:	n/a	n/a
20	TBP	chr5:92908622-92908834	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr5:92908780-92908930	HBMEC	blood vessel:	n/a	n/a
22	POLR2A	chr5:92908524-92908987	H1-neurons	neurons:	n/a	n/a
23	GABPA	chr5:92908458-92909016	H1-hESC	embryonic stem cell:	n/a	chr5:92908700-92908714
24	MAX	chr5:92907556-92908977	H1-hESC	embryonic stem cell:	n/a	chr5:92907848-92907855 chr5:92907847-92907856 chr5:92907846-92907857 chr5:92908748-92908758 chr5:92907847-92907857 chr5:92907846-92907857 chr5:92907846-92907857 chr5:92907847-92907856 chr5:92907845-92907858 chr5:92907846-92907856
25	FOXP2	chr5:92908471-92908822	PFSK-1	brain:	n/a	n/a
26	ZNF263	chr5:92908695-92909025	HEK293-T-REx	kidney:	n/a	chr5:92908885-92908906
27	SUZ12	chr5:92906819-92911054	NT2-D1	testis:	n/a	n/a
28	EGR1	chr5:92908511-92909060	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:92908771-92908821	GM12892	blood:	n/a
2	chr5:92908771-92908821	ECC-1	luminal epithelium:	n/a
3	chr5:92908771-92908821	HRE	kidney:	n/a
4	chr5:92908771-92908821	BJ	skin:	n/a
5	chr5:92908771-92908821	T-47D	breast:	n/a
6	chr5:92908771-92908821	SAEC	small airway:	n/a
7	chr5:92908771-92908821	GM12891	blood:	n/a
8	chr5:92908771-92908821	SK-N-SH	brain:	n/a
9	chr5:92908771-92908821	K562	blood:	n/a
10	chr5:92908771-92908821	AoSMC	blood vessel:	n/a
11	chr5:92908771-92908821	HCT-116	colon:	n/a
12	chr5:92908771-92908821	HRCEpiC	kidney:	n/a
13	chr5:92908771-92908821	NHDF-neo	bronchial:	n/a
14	chr5:92908771-92908821	HNPCEpiC	eye:	n/a
15	chr5:92908771-92908821	MCF-7	breast:	n/a
16	chr5:92908771-92908821	MCF10A-Er-Src	breast:	n/a
17	chr5:92908771-92908821	LNCaP	prostate:	n/a
18	chr5:92908771-92908821	HCPEpiC	choroid plexus:	n/a
19	chr5:92908771-92908821	NB4	blood:	n/a
20	chr5:92908771-92908821	HL-60	blood:	n/a
21	chr5:92908771-92908821	SK-N-SH_RA	brain:	n/a
22	chr5:92908771-92908821	HMEC	breast:	n/a
23	chr5:92908771-92908821	AG04450	lung:	fetal
24	chr5:92908771-92908821	NT2-D1	testis:	n/a
25	chr5:92908771-92908821	HAEpiC	amniotic membrane:	n/a
26	chr5:92908771-92908821	Jurkat	blood:	n/a
27	chr5:92908771-92908821	SK-N-MC	brain:	n/a
28	chr5:92908771-92908821	RPTEC	kidney:	n/a
29	chr5:92908771-92908821	NH-A	brain:	n/a
30	chr5:92908771-92908821	GM12878	blood:	n/a
31	chr5:92908771-92908821	Caco-2	colon:	n/a
32	chr5:92908771-92908821	AG09309	skin:	n/a
33	chr5:92908771-92908821	HCF	heart:	n/a
34	chr5:92908771-92908821	PANC-1	pancreas:	n/a
35	chr5:92908771-92908821	HEEpiC	esophagus:	n/a
36	chr5:92908771-92908821	HCM	heart:	n/a
37	chr5:92908771-92908821	HUVEC	blood vessel:	n/a
38	chr5:92908771-92908821	HIPEpiC	eye:	n/a
39	chr5:92908771-92908821	A549	lung:	n/a
40	chr5:92908771-92908821	AG09319	gingival:	n/a
41	chr5:92908771-92908821	PFSK-1	brain:	n/a
42	chr5:92908771-92908821	CMK	blood:	n/a
43	chr5:92908771-92908821	U87	brain:	n/a
44	chr5:92908771-92908821	SKMC	muscle:	n/a
45	chr5:92908771-92908821	GM06990	blood:	n/a
46	chr5:92908771-92908821	AG10803	skin:	n/a
47	chr5:92908771-92908821	HEK293	kidney:	embryo
48	chr5:92908771-92908821	Hepatocyte	liver:	n/a
49	chr5:92908771-92908821	HRPEpiC	eye:	n/a
50	chr5:92908771-92908821	HPAEpiC	pulmonary alveolar:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NR2F1-1	chr5:92908567-92908913	XLOC_004475
2	lnc-NR2F1-1	chr5:92908567-92908957	NONHSAT102813
3	lnc-NR2F1-1	chr5:92908567-92908913	NONHSAT102810
4	lnc-NR2F1-1	chr5:92908360-92908913	XLOC_004475

No data

Variant related genes	Relation type
NR2F1-AS1	TF binding region
NR2F1-AS1	CpG island

Extended variants
information (count: 107 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10041792	0.88[JPT][hapmap]
rs1004941	0.88[JPT][hapmap]
rs10050364	0.86[JPT][hapmap]
rs10051878	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10060331	0.86[JPT][hapmap]
rs10067541	0.88[JPT][hapmap]
rs10071040	0.88[JPT][hapmap]
rs1038686	0.86[JPT][hapmap]
rs1046217	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10476520	0.88[JPT][hapmap]
rs10514376	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11135388	0.86[EUR][1000 genomes]
rs11951859	0.83[EUR][1000 genomes]
rs11952115	0.89[EUR][1000 genomes]
rs11952600	0.85[EUR][1000 genomes]
rs11960608	0.89[EUR][1000 genomes]
rs12186735	0.93[ASN][1000 genomes]
rs12187239	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12188716	0.93[ASN][1000 genomes]
rs12188845	0.85[EUR][1000 genomes]
rs12188905	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13154650	0.86[JPT][hapmap]
rs13161885	0.86[JPT][hapmap]
rs1370977	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1457101	0.86[EUR][1000 genomes]
rs17082127	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17082129	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17083145	0.83[EUR][1000 genomes]
rs17083155	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17083181	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17083191	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17083194	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17083198	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17083200	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17083213	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17083228	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17083278	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17083297	0.86[JPT][hapmap]
rs17312456	0.86[JPT][hapmap]
rs17370695	0.93[ASN][1000 genomes]
rs1824153	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1844343	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2083227	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2279473	0.93[ASN][1000 genomes]
rs2344387	0.85[EUR][1000 genomes]
rs3776601	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs55861967	0.83[EUR][1000 genomes]
rs57165666	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57690257	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59360932	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61324921	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61352323	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6556823	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6556824	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6556829	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs6866771	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6877616	0.86[JPT][hapmap]
rs6879816	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6880843	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6881815	0.86[JPT][hapmap]
rs6884138	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6889857	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6890998	0.86[JPT][hapmap]
rs6895356	0.88[JPT][hapmap]
rs6898507	0.86[JPT][hapmap]
rs73133214	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73133217	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73133226	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73133228	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73133239	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73133251	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133254	0.83[EUR][1000 genomes]
rs73133258	0.85[EUR][1000 genomes]
rs73133261	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133265	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133275	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133278	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133280	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133282	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133283	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133287	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133289	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133292	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73133301	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73135313	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73135320	0.93[ASN][1000 genomes]
rs73135321	0.93[ASN][1000 genomes]
rs73772907	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7702348	0.88[JPT][hapmap]
rs7702649	0.86[JPT][hapmap]
rs7712388	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7715034	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7717718	0.88[JPT][hapmap]
rs7721168	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7721509	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs7727107	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7736624	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9314086	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022355	chr5:92846496-92911797	Weak transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	n/a
2	nsv537807	chr5:92846496-92911797	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	n/a
3	esv3451945	chr5:92858750-93024740	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv830404	chr5:92868336-93048257	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	esv1819334	chr5:92892591-92956733	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv882383	chr5:92895401-92928346	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv823130	chr5:92896346-92966016	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv4918	chr5:92898426-92943359	Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
9	nsv823132	chr5:92898512-92969668	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92889600-92909800	Weak transcription	Ovary	ovary
2	chr5:92900800-92914400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr5:92905400-92910200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:92905600-92908800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr5:92905600-92908800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:92905600-92909400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr5:92905600-92909600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:92905600-92909600	ZNF genes & repeats	Placenta	Placenta
9	chr5:92905800-92909600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:92906000-92909000	Bivalent Enhancer	Spleen	Spleen
11	chr5:92906000-92909200	Enhancers	Pancreas	Pancrea
12	chr5:92906000-92911200	Bivalent Enhancer	Fetal Brain Male	brain
13	chr5:92906400-92909000	Bivalent Enhancer	Liver	Liver
14	chr5:92906600-92909000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
15	chr5:92906800-92908800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr5:92906800-92909000	Bivalent Enhancer	Fetal Thymus	thymus
17	chr5:92907000-92909000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
18	chr5:92907000-92909400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
19	chr5:92907200-92908800	Bivalent Enhancer	Fetal Intestine Small	intestine
20	chr5:92907400-92909000	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr5:92907600-92908800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:92907600-92908800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr5:92907600-92909000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr5:92907600-92909000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:92907600-92909000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:92907600-92909200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
27	chr5:92907600-92909200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
28	chr5:92907600-92909200	Active TSS	Fetal Kidney	kidney
29	chr5:92907600-92909200	Flanking Active TSS	HMEC	breast
30	chr5:92907600-92909400	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
31	chr5:92907600-92909600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr5:92907800-92908800	Bivalent/Poised TSS	Psoas Muscle	Psoas
33	chr5:92907800-92908800	Bivalent/Poised TSS	HepG2	liver
34	chr5:92907800-92909000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr5:92907800-92909000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr5:92907800-92909000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
37	chr5:92907800-92909000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:92907800-92909000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr5:92907800-92909000	Bivalent Enhancer	Lung	lung
40	chr5:92907800-92909000	Flanking Active TSS	HUVEC	blood vessel
41	chr5:92907800-92909000	Active TSS	Osteobl	bone
42	chr5:92907800-92909200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
43	chr5:92907800-92909200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
44	chr5:92907800-92909400	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
45	chr5:92907800-92910800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
46	chr5:92908000-92908800	Bivalent Enhancer	Esophagus	oesophagus
47	chr5:92908000-92908800	Active TSS	Right Atrium	heart
48	chr5:92908000-92909000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr5:92908000-92909000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr5:92908000-92909000	Bivalent/Poised TSS	Brain Anterior Caudate	brain

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