Variant report

Variant	rs13147679
Chromosome Location	chr4:776489-776490
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	GATA3	chr4:775618-776578	T-47D	breast:	n/a	n/a
2	POLR2A	chr4:774610-776508	Hela-S3	cervix:	n/a	n/a
3	EP300	chr4:775545-776570	T-47D	breast:	n/a	chr4:775742-775751
4	HEY1	chr4:775270-776626	HepG2	liver:	n/a	chr4:775795-775810 chr4:775739-775754 chr4:775402-775417
5	FOXA1	chr4:776045-776583	HepG2	liver:	n/a	chr4:776308-776323
6	POLR2A	chr4:775834-776653	HepG2	liver:	n/a	n/a
7	MYBL2	chr4:775273-776553	HepG2	liver:	n/a	n/a
8	SIN3AK20	chr4:775017-776701	MCF-7	breast:	n/a	n/a
9	POLR2A	chr4:770558-777225	HepG2	liver:	n/a	n/a
10	POLR2A	chr4:774947-776543	H1-neurons	neurons:	n/a	n/a
11	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
12	MYC	chr4:775957-776506	MCF-7	breast:	n/a	n/a
13	CREB1	chr4:775030-776659	HepG2	liver:	n/a	n/a
14	MTA3	chr4:774557-776573	GM12878	blood:	n/a	n/a
15	FOXA2	chr4:776097-776565	HepG2	liver:	n/a	n/a
16	YY1	chr4:775277-776510	SK-N-SH_RA	brain:	n/a	chr4:775408-775422 chr4:775413-775424
17	SP1	chr4:774830-776594	HCT-116	colon:	n/a	chr4:775795-775804 chr4:775768-775782 chr4:775032-775041 chr4:775737-775748 chr4:775489-775501 chr4:776077-776086 chr4:775491-775500 chr4:775490-775499 chr4:775491-775500 chr4:775103-775115 chr4:775643-775664 chr4:775104-775118 chr4:775456-775470 chr4:775489-775501
18	FOXA1	chr4:776076-776547	T-47D	breast:	n/a	chr4:776308-776323
19	MAX	chr4:775295-776651	MCF-7	breast:	n/a	n/a
20	GATA3	chr4:775692-776562	T-47D	breast:	n/a	n/a
21	REST	chr4:775869-776584	SK-N-SH	brain:	n/a	chr4:776078-776091
22	KAP1	chr4:775403-776535	HEK293	kidney:	n/a	n/a
23	POLR2A	chr4:775284-776544	SK-N-SH	brain:	n/a	n/a
24	ELF1	chr4:775530-776524	HepG2	liver:	n/a	n/a
25	GABPA	chr4:775623-776517	MCF-7	breast:	n/a	chr4:775742-775751
26	POLR2A	chr4:775152-776493	HepG2	liver:	n/a	n/a
27	POLR2A	chr4:772569-776645	HepG2	liver:	n/a	n/a
28	JUN	chr4:774457-776546	K562	blood:	n/a	chr4:775226-775237 chr4:774840-774852 chr4:775717-775726 chr4:774841-774850 chr4:774842-774851 chr4:775652-775661
29	POLR2A	chr4:775197-776558	HepG2	liver:	n/a	n/a
30	PBX3	chr4:775339-776576	SK-N-SH	brain:	n/a	chr4:775718-775727
31	ZNF263	chr4:775355-776561	HEK293-T-REx	kidney:	n/a	chr4:775994-776003
32	HDAC2	chr4:776091-776634	MCF-7	breast:	n/a	n/a
33	MAX	chr4:775766-776529	MCF-7	breast:	n/a	n/a
34	POLR2A	chr4:776428-776575	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr4:775848-776514	HepG2	liver:	n/a	n/a
36	GATA3	chr4:775704-776594	MCF-7	breast:	n/a	n/a
37	GATA3	chr4:775631-776702	MCF-7	breast:	n/a	n/a
38	MXI1	chr4:775157-776544	HepG2	liver:	n/a	n/a
39	MAZ	chr4:774419-776694	IMR90	lung:	n/a	chr4:774841-774850
40	FOXA1	chr4:775532-776555	T-47D	breast:	n/a	chr4:776308-776323
41	ELF1	chr4:775526-776673	MCF-7	breast:	n/a	n/a
42	POLR2A	chr4:775222-776738	MCF-7	breast:	n/a	n/a
43	POLR2A	chr4:775775-776506	HepG2	liver:	n/a	n/a
44	YY1	chr4:774876-776565	H1-hESC	embryonic stem cell:	n/a	chr4:775074-775083 chr4:775408-775422 chr4:775078-775100 chr4:775192-775201 chr4:775413-775424
45	KAP1	chr4:775565-776495	U2OS	brain:	n/a	n/a
46	FOXA1	chr4:776077-776602	HepG2	liver:	n/a	chr4:776308-776323
47	MXI1	chr4:774159-776504	IMR90	lung:	n/a	n/a
48	USF1	chr4:775090-776577	HCT-116	colon:	n/a	chr4:775406-775422 chr4:775398-775414 chr4:775735-775751
49	TAF1	chr4:775126-776525	ECC-1	luminal epithelium:	n/a	n/a
50	POLR2A	chr4:772621-776617	K562	blood:	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	chr15:70760462..70762152-chr4:775957..778885,2	MCF-7	breast:
5	chr4:671080..676330-chr4:771868..776883,7	K562	blood:
6	chr4:775742..777793-chr4:821294..823838,2	MCF-7	breast:
7	chr4:677843..680231-chr4:776162..778383,2	MCF-7	breast:
8	chr4:773678..778564-chr4:818343..821273,5	K562	blood:
9	chr4:775968..777707-chr4:794357..796914,2	MCF-7	breast:
10	chr4:735917..738355-chr4:773628..776647,3	MCF-7	breast:
11	chr4:774335..777276-chr4:923482..926205,2	K562	blood:
12	chr4:774443..776550-chr4:1003219..1006058,2	MCF-7	breast:
13	chr4:774284..777559-chr4:817781..820963,6	MCF-7	breast:
14	chr4:758084..763800-chr4:770671..778725,12	MCF-7	breast:
15	chr4:774211..776951-chr4:981590..984228,3	MCF-7	breast:
16	chr4:666044..670200-chr4:772961..777371,6	K562	blood:

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

Extended variants
information (count: 45 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs13105255	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13105473	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13105702	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13122480	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13127293	0.82[AFR][1000 genomes]
rs13131168	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13131185	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13136722	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13138362	0.82[AFR][1000 genomes]
rs13151247	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1564279	0.95[AFR][1000 genomes]
rs2242237	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28497436	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34959417	0.81[ASN][1000 genomes]
rs35333201	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4234854	0.84[ASN][1000 genomes]
rs6811216	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6819857	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6838241	0.84[ASN][1000 genomes]
rs6840352	0.83[AFR][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

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs13147679	PCGF3	cis	Artery Tibial	GTEx
rs13147679	CPLX1	cis	Thyroid	GTEx
rs13147679	AC139887.4	cis	Nerve Tibial	GTEx
rs13147679	RP11-440L14.1	cis	Artery Tibial	GTEx
rs13147679	AC139887.4	cis	Artery Tibial	GTEx
rs13147679	CPLX1	cis	Esophagus Muscularis	GTEx

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:774400-776600	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr4:774600-776600	Active TSS	Ovary	ovary
3	chr4:774800-776600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:775000-776600	Active TSS	Fetal Brain Female	brain
5	chr4:775000-776800	Active TSS	Rectal Smooth Muscle	rectum
6	chr4:776000-776600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:776000-776600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr4:776000-776600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr4:776000-776600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:776000-776600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:776000-776600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr4:776000-776600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr4:776000-776600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr4:776000-776600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr4:776000-776600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:776000-776600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
17	chr4:776000-776600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
18	chr4:776000-776600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr4:776000-776600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr4:776000-776600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:776000-776600	Flanking Active TSS	Adipose Nuclei	Adipose
22	chr4:776000-776600	Flanking Active TSS	Brain Germinal Matrix	brain
23	chr4:776000-776600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
24	chr4:776000-776600	Flanking Active TSS	Colonic Mucosa	Colon
25	chr4:776000-776600	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr4:776000-776600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr4:776000-776600	Flanking Active TSS	Fetal Brain Male	brain
28	chr4:776000-776600	Flanking Active TSS	Fetal Heart	heart
29	chr4:776000-776600	Flanking Active TSS	Fetal Intestine Large	intestine
30	chr4:776000-776600	Flanking Active TSS	Fetal Intestine Small	intestine
31	chr4:776000-776600	Flanking Active TSS	Fetal Muscle Trunk	muscle
32	chr4:776000-776600	Flanking Active TSS	Fetal Stomach	stomach
33	chr4:776000-776600	Flanking Active TSS	Pancreas	Pancrea
34	chr4:776000-776600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
35	chr4:776000-776600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr4:776000-776600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr4:776000-776600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr4:776000-776600	Flanking Active TSS	Stomach Smooth Muscle	stomach
39	chr4:776000-776600	Flanking Active TSS	Dnd41	blood
40	chr4:776000-776600	Flanking Bivalent TSS/Enh	HepG2	liver
41	chr4:776000-776600	Flanking Active TSS	HMEC	breast
42	chr4:776000-776600	Flanking Active TSS	Osteobl	bone
43	chr4:776000-777000	Flanking Active TSS	Placenta	Placenta
44	chr4:776200-776600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
45	chr4:776200-776600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:776200-776600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr4:776200-776600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:776200-776600	Flanking Active TSS	Brain Angular Gyrus	brain
49	chr4:776200-776600	Flanking Active TSS	Brain Anterior Caudate	brain
50	chr4:776200-776600	Flanking Active TSS	Brain Cingulate Gyrus	brain

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