Variant report

Variant	rs3763072
Chromosome Location	chr5:89769647-89769648
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	SIN3AK20	chr5:89769506-89771120	HCT-116	colon:	n/a	n/a
2	MAFK	chr5:89768418-89769702	GM12878	blood:	n/a	chr5:89768782-89768797
3	SP1	chr5:89769624-89771184	A549	lung:	n/a	chr5:89770632-89770644 chr5:89770239-89770249 chr5:89770655-89770665 chr5:89770654-89770666 chr5:89770634-89770643 chr5:89770655-89770665 chr5:89770633-89770642 chr5:89770858-89770871 chr5:89770651-89770665 chr5:89770656-89770665 chr5:89770654-89770666 chr5:89770629-89770643 chr5:89770633-89770643 chr5:89770632-89770644 chr5:89770893-89770900 chr5:89770655-89770664 chr5:89770633-89770643
4	KAP1	chr5:89768970-89771055	HEK293	kidney:	n/a	n/a
5	TBP	chr5:89768894-89771288	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr5:89769382-89771008	A549	lung:	n/a	n/a
7	TBP	chr5:89769047-89770954	H1-hESC	embryonic stem cell:	n/a	n/a
8	E2F1	chr5:89769562-89770892	Hela-S3	cervix:	n/a	n/a
9	ETS1	chr5:89769514-89770836	K562	blood:	n/a	chr5:89770234-89770245
10	USF2	chr5:89769623-89770058	GM12878	blood:	n/a	n/a
11	PAX5	chr5:89769558-89770934	GM12892	blood:	n/a	n/a
12	POLR2A	chr5:89769089-89770975	NB4	blood:	n/a	n/a
13	POLR2A	chr5:89769432-89771148	PFSK-1	brain:	n/a	n/a
14	HCFC1	chr5:89769470-89771033	K562	blood:	n/a	n/a
15	MAZ	chr5:89769006-89771106	IMR90	lung:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907
16	BACH1	chr5:89769103-89771002	H1-hESC	embryonic stem cell:	n/a	n/a
17	EGR1	chr5:89769270-89770930	HCT-116	colon:	n/a	chr5:89770237-89770246 chr5:89770234-89770248 chr5:89770650-89770663 chr5:89770651-89770662 chr5:89770515-89770522 chr5:89770650-89770663 chr5:89770649-89770664 chr5:89770514-89770529 chr5:89770514-89770528 chr5:89770234-89770247 chr5:89770234-89770247 chr5:89770234-89770247 chr5:89770655-89770665 chr5:89770235-89770246 chr5:89770233-89770248 chr5:89770234-89770247 chr5:89770515-89770528 chr5:89770139-89770149 chr5:89770515-89770528 chr5:89770230-89770252 chr5:89770650-89770664
18	RCOR1	chr5:89769068-89771039	Hela-S3	cervix:	n/a	n/a
19	E2F6	chr5:89769070-89771102	K562	blood:	n/a	n/a
20	TEAD4	chr5:89769605-89770940	ECC-1	luminal epithelium:	n/a	n/a
21	MYC	chr5:89769545-89770885	K562	blood:	n/a	chr5:89770655-89770665 chr5:89770234-89770244
22	POLR2A	chr5:89769058-89770947	K562	blood:	n/a	n/a
23	CREB1	chr5:89769518-89770905	A549	lung:	n/a	n/a
24	HEY1	chr5:89768926-89769657	K562	blood:	n/a	n/a
25	EGR1	chr5:89769632-89770963	K562	blood:	n/a	chr5:89770237-89770246 chr5:89770234-89770248 chr5:89770650-89770663 chr5:89770651-89770662 chr5:89770515-89770522 chr5:89770650-89770663 chr5:89770649-89770664 chr5:89770514-89770529 chr5:89770514-89770528 chr5:89770234-89770247 chr5:89770234-89770247 chr5:89770234-89770247 chr5:89770655-89770665 chr5:89770235-89770246 chr5:89770233-89770248 chr5:89770234-89770247 chr5:89770515-89770528 chr5:89770139-89770149 chr5:89770515-89770528 chr5:89770230-89770252 chr5:89770650-89770664
26	CHD2	chr5:89769110-89770896	K562	blood:	n/a	n/a
27	POLR2A	chr5:89769032-89771013	K562	blood:	n/a	n/a
28	MAX	chr5:89769021-89771203	HepG2	liver:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907
29	YY1	chr5:89769624-89770910	K562	blood:	n/a	chr5:89770236-89770245 chr5:89770344-89770358 chr5:89770384-89770395 chr5:89770379-89770393
30	POLR2A	chr5:89769207-89770953	GM18526	blood:	n/a	n/a
31	POLR2A	chr5:89769113-89770990	GM18505	blood:	n/a	n/a
32	MAX	chr5:89769264-89771071	HepG2	liver:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907
33	MAX	chr5:89769367-89771037	K562	blood:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907
34	MAX	chr5:89769382-89771053	MCF-7	breast:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907
35	POLR2A	chr5:89769017-89771079	GM12878	blood:	n/a	n/a
36	MAX	chr5:89769597-89771004	HUVEC	blood vessel:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907
37	POLR2A	chr5:89768999-89771072	GM12892	blood:	n/a	n/a
38	MYC	chr5:89769071-89771203	K562	blood:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907
39	YY1	chr5:89769476-89770973	GM12878	blood:	n/a	chr5:89770236-89770245 chr5:89770344-89770358 chr5:89770384-89770395 chr5:89770379-89770393
40	BRCA1	chr5:89768969-89769720	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr5:89768908-89771346	MCF10A-Er-Src	breast:	n/a	n/a
42	ELF1	chr5:89769538-89769837	HepG2	liver:	n/a	n/a
43	TCF7L2	chr5:89768971-89770924	Hela-S3	cervix:	n/a	n/a
44	SMARCB1	chr5:89769094-89771066	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr5:89768952-89770824	K562	blood:	n/a	n/a
46	TEAD4	chr5:89769574-89770947	ECC-1	luminal epithelium:	n/a	n/a
47	MAX	chr5:89769065-89771142	NB4	blood:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907
48	TCF12	chr5:89769623-89770022	A549	lung:	n/a	n/a
49	E2F6	chr5:89769517-89770026	K562	blood:	n/a	n/a
50	MAX	chr5:89769143-89771145	MCF-7	breast:	n/a	chr5:89770655-89770665 chr5:89770897-89770908 chr5:89770234-89770244 chr5:89770899-89770906 chr5:89770897-89770907

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:89769642-89769692	BE2_C	brain:	n/a
2	chr5:89769642-89769692	HEEpiC	esophagus:	n/a
3	chr5:89769642-89769692	HAEpiC	amniotic membrane:	n/a
4	chr5:89769642-89769692	HIPEpiC	eye:	n/a
5	chr5:89769642-89769692	AG09309	skin:	n/a
6	chr5:89769642-89769692	U87	brain:	n/a
7	chr5:89769642-89769692	HNPCEpiC	eye:	n/a
8	chr5:89769642-89769692	HEK293	kidney:	embryo
9	chr5:89769642-89769692	AG09319	gingival:	n/a
10	chr5:89769642-89769692	LNCaP	prostate:	n/a
11	chr5:89769642-89769692	SK-N-MC	brain:	n/a
12	chr5:89769642-89769692	AG04449	skin:	fetal
13	chr5:89769642-89769692	RPTEC	kidney:	n/a
14	chr5:89769642-89769692	HCF	heart:	n/a
15	chr5:89769642-89769692	PrEC	prostate:	n/a
16	chr5:89769642-89769692	H1-hESC	embryonic stem cell:	embryo
17	chr5:89769642-89769692	HRCEpiC	kidney:	n/a
18	chr5:89769642-89769692	HCPEpiC	choroid plexus:	n/a
19	chr5:89769642-89769692	AoSMC	blood vessel:	n/a
20	chr5:89769642-89769692	HepG2	liver:	n/a
21	chr5:89769642-89769692	MCF-7	breast:	n/a
22	chr5:89769642-89769692	GM12892	blood:	n/a
23	chr5:89769642-89769692	HL-60	blood:	n/a
24	chr5:89769642-89769692	NT2-D1	testis:	n/a
25	chr5:89769642-89769692	Hela-S3	cervix:	n/a
26	chr5:89769642-89769692	NH-A	brain:	n/a
27	chr5:89769642-89769692	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:89769642-89769692	SK-N-SH	brain:	n/a
29	chr5:89769642-89769692	K562	blood:	n/a
30	chr5:89769642-89769692	SKMC	muscle:	n/a
31	chr5:89769642-89769692	HRPEpiC	eye:	n/a
32	chr5:89769642-89769692	NB4	blood:	n/a
33	chr5:89769642-89769692	GM19239	blood:	n/a
34	chr5:89769642-89769692	GM12891	blood:	n/a
35	chr5:89769642-89769692	HUVEC	blood vessel:	n/a
36	chr5:89769642-89769692	PFSK-1	brain:	n/a
37	chr5:89769642-89769692	NHBE	bronchial:	n/a
38	chr5:89769642-89769692	CMK	blood:	n/a
39	chr5:89769642-89769692	Caco-2	colon:	n/a
40	chr5:89769642-89769692	HCM	heart:	n/a
41	chr5:89769642-89769692	ECC-1	luminal epithelium:	n/a
42	chr5:89769642-89769692	AG04450	lung:	fetal
43	chr5:89769642-89769692	MCF10A-Er-Src	breast:	n/a
44	chr5:89769642-89769692	PANC-1	pancreas:	n/a
45	chr5:89769642-89769692	GM12878	blood:	n/a
46	chr5:89769642-89769692	T-47D	breast:	n/a
47	chr5:89769642-89769692	ovcar-3	ovarian:	n/a
48	chr5:89769642-89769692	HMEC	breast:	n/a
49	chr5:89769642-89769692	GM06990	blood:	n/a
50	chr5:89769642-89769692	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:89769110..89772331-chr5:90086907..90091587,4	K562	blood:
2	chr5:89769550..89772254-chr5:89851679..89856622,6	MCF-7	breast:
3	chr1:210547411..210548099-chr5:89769614..89770507,2	Hela-S3	cervix:
4	chr5:89704491..89706992-chr5:89769088..89771566,3	MCF-7	breast:
5	chr5:89768855..89773751-chr5:89822671..89829297,12	K562	blood:
6	chr5:89702524..89708084-chr5:89764247..89773389,22	K562	blood:
7	chr5:89767818..89772796-chr5:89823286..89827702,11	MCF-7	breast:
8	chr5:89768685..89771799-chr5:89852676..89855842,6	MCF-7	breast:
9	chr5:89768584..89771978-chr5:90675764..90678297,3	K562	blood:
10	chr5:89768691..89773005-chr5:89822332..89827140,9	MCF-7	breast:
11	chr5:89766469..89774126-chr5:89823341..89829105,11	K562	blood:
12	chr5:89764343..89768380-chr5:89768675..89771583,10	MCF-7	breast:
13	chr5:89701553..89708894-chr5:89768084..89771807,14	K562	blood:
14	chr5:89769121..89772256-chr5:89935164..89938437,4	K562	blood:
15	chr5:89703543..89706963-chr5:89767513..89771420,6	MCF-7	breast:

Variant related genes	Relation type
POLR3G	TF binding region
POLR3G	CpG island
ENSG00000113369	Chromatin interaction
ENSG00000153140	Chromatin interaction
ENSG00000200972	Chromatin interaction
ENSG00000255647	Chromatin interaction
ENSG00000164199	Chromatin interaction
ENSG00000176018	Chromatin interaction
ENSG00000113356	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10041220	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10043702	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10214167	0.90[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10473934	1.00[CEU][hapmap];0.98[GIH][hapmap];0.92[MEX][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10942593	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10942594	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11953207	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11956418	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12516555	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13436287	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2303801	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28728101	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28815472	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2914674	0.82[CHB][hapmap];0.84[JPT][hapmap]
rs34397682	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3763070	0.90[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3805478	0.95[CEU][hapmap];0.86[CHB][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59742368	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61610742	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6864062	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6867534	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6872360	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6889253	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6889947	0.90[ASW][hapmap];1.00[CEU][hapmap];0.98[GIH][hapmap];0.96[MEX][hapmap];0.97[TSI][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6890115	0.90[ASW][hapmap];1.00[CEU][hapmap];0.98[GIH][hapmap];0.96[MEX][hapmap];0.97[TSI][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7729481	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7730433	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7732363	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021142	chr5:89102893-89897826	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv537804	chr5:89102893-89897826	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv917025	chr5:89208994-89855436	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
7	nsv518131	chr5:89748142-89781594	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases
8	nsv882364	chr5:89748142-89808531	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89768200-89771400	Active TSS	GM12878-XiMat	blood
2	chr5:89768400-89770200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:89768400-89770400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
4	chr5:89768400-89771200	Active TSS	Brain Angular Gyrus	brain
5	chr5:89768600-89770000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:89768600-89770000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:89768600-89770800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:89768600-89771200	Flanking Active TSS	Stomach Smooth Muscle	stomach
9	chr5:89768600-89771600	Active TSS	NHDF-Ad	bronchial
10	chr5:89768600-89772000	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr5:89768800-89769800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:89768800-89769800	Flanking Active TSS	Primary T cells from cord blood	blood
13	chr5:89768800-89769800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr5:89768800-89769800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr5:89768800-89769800	Active TSS	Right Atrium	heart
16	chr5:89768800-89770000	Flanking Active TSS	Liver	Liver
17	chr5:89768800-89770200	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr5:89768800-89770200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr5:89768800-89770200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr5:89768800-89770400	Flanking Active TSS	Primary hematopoietic stem cells	blood
21	chr5:89768800-89770400	Flanking Active TSS	Adipose Nuclei	Adipose
22	chr5:89768800-89770800	Active TSS	NHLF	lung
23	chr5:89768800-89771200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr5:89768800-89771200	Active TSS	Fetal Heart	heart
25	chr5:89768800-89771200	Active TSS	Ovary	ovary
26	chr5:89768800-89771400	Active TSS	Fetal Intestine Large	intestine
27	chr5:89768800-89771400	Active TSS	A549	lung
28	chr5:89768800-89771600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:89768800-89771600	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr5:89768800-89772000	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr5:89768800-89773200	Active TSS	H9 Cell Line	embryonic stem cell
32	chr5:89768800-89773400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr5:89769000-89769800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr5:89769000-89769800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
35	chr5:89769000-89769800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr5:89769000-89769800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr5:89769000-89769800	Flanking Active TSS	Fetal Brain Male	brain
38	chr5:89769000-89769800	Flanking Active TSS	Fetal Muscle Leg	muscle
39	chr5:89769000-89769800	Flanking Active TSS	NH-A	brain
40	chr5:89769000-89770000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
41	chr5:89769000-89770000	Flanking Active TSS	K562	blood
42	chr5:89769000-89770200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr5:89769000-89770200	Flanking Active TSS	Colonic Mucosa	Colon
44	chr5:89769000-89770400	Flanking Active TSS	Lung	lung
45	chr5:89769000-89770400	Bivalent/Poised TSS	HepG2	liver
46	chr5:89769000-89770800	Active TSS	Fetal Intestine Small	intestine
47	chr5:89769000-89770800	Active TSS	Gastric	stomach
48	chr5:89769000-89770800	Active TSS	Stomach Mucosa	stomach
49	chr5:89769000-89771000	Active TSS	Pancreas	Pancrea
50	chr5:89769000-89771200	Active TSS	Esophagus	oesophagus

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