Variant report

Variant	rs55974756
Chromosome Location	chr4:776137-776138
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NR2F2	chr4:775016-776275	K562	blood:	n/a	n/a
2	ZMIZ1	chr4:775940-776216	K562	blood:	n/a	n/a
3	TAF1	chr4:775201-776465	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr4:775866-776222	A549	lung:	n/a	n/a
5	YY1	chr4:774875-776448	GM12878	blood:	n/a	chr4:775074-775083 chr4:775408-775422 chr4:775078-775100 chr4:775192-775201 chr4:775413-775424
6	MYC	chr4:775887-776296	K562	blood:	n/a	n/a
7	GATA3	chr4:775618-776578	T-47D	breast:	n/a	n/a
8	NFIC	chr4:775465-776364	HepG2	liver:	n/a	n/a
9	PBX3	chr4:776106-776286	GM12878	blood:	n/a	n/a
10	MYC	chr4:775106-776294	K562	blood:	n/a	n/a
11	MYC	chr4:775126-776368	K562	blood:	n/a	n/a
12	HMGN3	chr4:774971-776238	K562	blood:	n/a	n/a
13	POLR2A	chr4:774610-776508	Hela-S3	cervix:	n/a	n/a
14	EP300	chr4:775545-776570	T-47D	breast:	n/a	chr4:775742-775751
15	STAT3	chr4:775717-776253	MCF10A-Er-Src	breast:	n/a	chr4:775772-775784 chr4:775895-775906
16	BRCA1	chr4:776087-776194	H1-hESC	embryonic stem cell:	n/a	n/a
17	EP300	chr4:776014-776368	HepG2	liver:	n/a	n/a
18	POLR2A	chr4:775321-776317	HCT-116	colon:	n/a	n/a
19	HEY1	chr4:775270-776626	HepG2	liver:	n/a	chr4:775795-775810 chr4:775739-775754 chr4:775402-775417
20	FOXA1	chr4:776045-776583	HepG2	liver:	n/a	chr4:776308-776323
21	STAT1	chr4:775223-776141	GM12878	blood:	n/a	chr4:775772-775784 chr4:775414-775426
22	POLR2A	chr4:775834-776653	HepG2	liver:	n/a	n/a
23	MYBL2	chr4:775273-776553	HepG2	liver:	n/a	n/a
24	POLR2A	chr4:775338-776233	SK-N-MC	brain:	n/a	n/a
25	POLR2A	chr4:775284-776261	K562	blood:	n/a	n/a
26	POLR2A	chr4:775379-776390	GM12878	blood:	n/a	n/a
27	POLR2A	chr4:775305-776330	A549	lung:	n/a	n/a
28	SIN3AK20	chr4:775017-776701	MCF-7	breast:	n/a	n/a
29	PML	chr4:775178-776247	K562	blood:	n/a	n/a
30	YY1	chr4:775231-776260	K562	blood:	n/a	chr4:775408-775422 chr4:775413-775424
31	MAX	chr4:775370-776483	HepG2	liver:	n/a	n/a
32	RCOR1	chr4:775532-776185	Hela-S3	cervix:	n/a	n/a
33	MAX	chr4:775185-776372	K562	blood:	n/a	n/a
34	POLR2A	chr4:775293-776261	K562	blood:	n/a	n/a
35	POLR2A	chr4:770558-777225	HepG2	liver:	n/a	n/a
36	MAX	chr4:775383-776356	A549	lung:	n/a	n/a
37	TAF1	chr4:775068-776322	HepG2	liver:	n/a	n/a
38	MXI1	chr4:775487-776310	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr4:775405-776233	Hela-S3	cervix:	n/a	n/a
40	BHLHE40	chr4:775249-776374	K562	blood:	n/a	chr4:775406-775422 chr4:775398-775414 chr4:775735-775751
41	POLR2A	chr4:774947-776543	H1-neurons	neurons:	n/a	n/a
42	POLR2A	chr4:775823-776353	U87	brain:	n/a	n/a
43	CREB1	chr4:775249-776454	GM12878	blood:	n/a	n/a
44	POLR2A	chr4:772703-776479	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr4:774729-776399	NB4	blood:	n/a	n/a
46	TBL1XR1	chr4:775435-776161	K562	blood:	n/a	n/a
47	SP1	chr4:775427-776504	HepG2	liver:	n/a	chr4:775795-775804 chr4:775768-775782 chr4:775737-775748 chr4:775489-775501 chr4:776077-776086 chr4:775491-775500 chr4:775490-775499 chr4:775491-775500 chr4:775643-775664 chr4:775456-775470 chr4:775489-775501
48	MYC	chr4:775957-776506	MCF-7	breast:	n/a	n/a
49	HCFC1	chr4:775183-776352	Hela-S3	cervix:	n/a	n/a
50	CREB1	chr4:775030-776659	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:679737..681440-chr4:774148..776582,2	K562	blood:
2	chr4:735724..738302-chr4:774438..777111,2	MCF-7	breast:
3	chr4:774894..778846-chr4:965454..968160,4	MCF-7	breast:
4	chr4:773572..776391-chr4:979959..982266,2	MCF-7	breast:
5	chr15:70760462..70762152-chr4:775957..778885,2	MCF-7	breast:
6	chr4:671080..676330-chr4:771868..776883,7	K562	blood:
7	chr4:775742..777793-chr4:821294..823838,2	MCF-7	breast:
8	chr4:775576..776177-chr6:27100717..27101262,2	Hela-S3	cervix:
9	chr4:773678..778564-chr4:818343..821273,5	K562	blood:
10	chr4:775968..777707-chr4:794357..796914,2	MCF-7	breast:
11	chr4:735917..738355-chr4:773628..776647,3	MCF-7	breast:
12	chr4:774335..777276-chr4:923482..926205,2	K562	blood:
13	chr4:773038..776439-chr4:923639..926176,4	MCF-7	breast:
14	chr4:774443..776550-chr4:1003219..1006058,2	MCF-7	breast:
15	chr4:774284..777559-chr4:817781..820963,6	MCF-7	breast:
16	chr4:758084..763800-chr4:770671..778725,12	MCF-7	breast:
17	chr19:30155987..30156547-chr4:775222..776214,2	NB4	blood:
18	chr4:774518..776312-chr4:2935741..2938166,2	MCF-7	breast:
19	chr4:774211..776951-chr4:981590..984228,3	MCF-7	breast:
20	chr4:666044..670200-chr4:772961..777371,6	K562	blood:

Variant related genes	Relation type
ENSG00000249592	TF binding region
ENSG00000166289	Chromatin interaction
ENSG00000249673	Chromatin interaction
ENSG00000127419	Chromatin interaction
ENSG00000185619	Chromatin interaction
ENSG00000169020	Chromatin interaction
ENSG00000127415	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000109736	Chromatin interaction
ENSG00000178950	Chromatin interaction
ENSG00000145214	Chromatin interaction
ENSG00000127418	Chromatin interaction
ENSG00000169026	Chromatin interaction
ENSG00000215375	Chromatin interaction
ENSG00000233799	Chromatin interaction
ENSG00000168993	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10004297	1.00[ASN][1000 genomes]
rs11930710	0.91[ASN][1000 genomes]
rs13111051	1.00[ASN][1000 genomes]
rs13145884	1.00[ASN][1000 genomes]
rs28587502	1.00[ASN][1000 genomes]
rs28638011	1.00[ASN][1000 genomes]
rs3733356	1.00[ASN][1000 genomes]
rs3733357	1.00[ASN][1000 genomes]
rs3816679	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3822027	1.00[ASN][1000 genomes]
rs4234855	1.00[ASN][1000 genomes]
rs55667166	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56074082	1.00[ASN][1000 genomes]
rs6811804	1.00[ASN][1000 genomes]
rs6815765	1.00[ASN][1000 genomes]
rs6838243	1.00[ASN][1000 genomes]
rs73207755	1.00[ASN][1000 genomes]
rs73222805	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222806	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222810	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222827	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222831	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222832	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73222841	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73222842	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7655749	1.00[ASN][1000 genomes]
rs7655941	1.00[ASN][1000 genomes]
rs7661962	1.00[ASN][1000 genomes]
rs7662167	1.00[ASN][1000 genomes]
rs7674850	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
5	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
9	esv1829397	chr4:655939-1041957	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
10	nsv878254	chr4:708932-899143	Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
11	nsv878255	chr4:708932-1052488	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
12	nsv878257	chr4:712222-852313	Strong transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
13	nsv878258	chr4:712222-1058358	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
14	nsv878259	chr4:713920-852313	Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv878260	chr4:713920-1052488	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
16	nsv818207	chr4:753944-821490	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
17	nsv878261	chr4:756686-1047794	Active TSS Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
18	nsv1007928	chr4:757263-813885	Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
19	nsv520136	chr4:759709-780883	ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
20	nsv1003219	chr4:769894-1105464	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
21	nsv515844	chr4:771587-780883	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
22	nsv526780	chr4:771587-786401	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
23	nsv521402	chr4:771587-793763	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
24	nsv878262	chr4:771587-865227	Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
25	nsv878263	chr4:771587-1047794	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:774000-776200	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr4:774000-776200	Active TSS	NHDF-Ad	bronchial
3	chr4:774200-776200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:774200-776200	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr4:774200-776200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:774200-776400	Active TSS	Gastric	stomach
7	chr4:774400-776200	Active TSS	Left Ventricle	heart
8	chr4:774400-776400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:774400-776400	Active TSS	Aorta	Aorta
10	chr4:774400-776400	Active TSS	Right Atrium	heart
11	chr4:774400-776400	Active TSS	Right Ventricle	heart
12	chr4:774400-776600	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr4:774600-776200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:774600-776200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:774600-776200	Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr4:774600-776200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:774600-776200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:774600-776200	Active TSS	Brain Anterior Caudate	brain
19	chr4:774600-776200	Active TSS	Brain Hippocampus Middle	brain
20	chr4:774600-776200	Active TSS	Fetal Kidney	kidney
21	chr4:774600-776200	Active TSS	Hela-S3	cervix
22	chr4:774600-776200	Active TSS	HSMMtube	muscle
23	chr4:774600-776400	Active TSS	H9 Cell Line	embryonic stem cell
24	chr4:774600-776400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
25	chr4:774600-776600	Active TSS	Ovary	ovary
26	chr4:774800-776200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr4:774800-776200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:774800-776200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr4:774800-776200	Active TSS	Brain Substantia Nigra	brain
30	chr4:774800-776200	Active TSS	Colon Smooth Muscle	Colon
31	chr4:774800-776200	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr4:774800-776200	Active TSS	Sigmoid Colon	Sigmoid Colon
33	chr4:774800-776200	Active TSS	Stomach Mucosa	stomach
34	chr4:774800-776200	Active TSS	A549	lung
35	chr4:774800-776400	Active TSS	Psoas Muscle	Psoas
36	chr4:774800-776600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:775000-776200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
38	chr4:775000-776200	Active TSS	Liver	Liver
39	chr4:775000-776200	Active TSS	Brain Angular Gyrus	brain
40	chr4:775000-776200	Active TSS	Brain Cingulate Gyrus	brain
41	chr4:775000-776200	Active TSS	Esophagus	oesophagus
42	chr4:775000-776600	Active TSS	Fetal Brain Female	brain
43	chr4:775000-776800	Active TSS	Rectal Smooth Muscle	rectum
44	chr4:775400-776200	Active TSS	Monocytes-CD14+_RO01746	blood
45	chr4:775600-776200	Weak transcription	Spleen	Spleen
46	chr4:776000-776200	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr4:776000-776200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr4:776000-776200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr4:776000-776200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr4:776000-776200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell

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