Variant report

Variant	rs7702303
Chromosome Location	chr5:178986436-178986437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:242)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:242 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TAF1	chr5:178986366-178986606	GM12878	blood:	n/a	n/a
2	YY1	chr5:178986325-178986855	NT2-D1	testis:	n/a	chr5:178986551-178986559
3	YY1	chr5:178986258-178986912	ECC-1	luminal epithelium:	n/a	chr5:178986551-178986559
4	CHD1	chr5:178985618-178986945	H1-hESC	embryonic stem cell:	n/a	n/a
5	MXI1	chr5:178985457-178987460	SK-N-SH	brain:	n/a	n/a
6	SIN3AK20	chr5:178986065-178987144	PANC-1	pancreas:	n/a	n/a
7	POLR2A	chr5:178985798-178987122	GM12878	blood:	n/a	n/a
8	YY1	chr5:178986331-178986698	HCT-116	colon:	n/a	chr5:178986551-178986559
9	TAF1	chr5:178985924-178986941	H1-hESC	embryonic stem cell:	n/a	n/a
10	STAT3	chr5:178986291-178986855	MCF10A-Er-Src	breast:	n/a	n/a
11	CEBPB	chr5:178986395-178987118	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr5:178986257-178987131	Gliobla	brain:	n/a	n/a
13	GTF2F1	chr5:178986337-178986705	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:178985889-178987010	A549	lung:	n/a	n/a
15	POLR2A	chr5:178986270-178987125	ECC-1	luminal epithelium:	n/a	n/a
16	TBP	chr5:178986329-178986776	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr5:178986261-178987092	A549	lung:	n/a	n/a
18	YY1	chr5:178986258-178986664	GM12892	blood:	n/a	chr5:178986551-178986559
19	SP1	chr5:178986183-178987120	A549	lung:	n/a	chr5:178986611-178986625 chr5:178986510-178986519 chr5:178986509-178986518 chr5:178986510-178986519 chr5:178986616-178986625 chr5:178986615-178986624 chr5:178986614-178986626 chr5:178986614-178986626
20	YY1	chr5:178986307-178986946	HepG2	liver:	n/a	chr5:178986551-178986559
21	MAX	chr5:178985914-178987175	SK-N-SH	brain:	n/a	n/a
22	POLR2A	chr5:178986334-178987012	HepG2	liver:	n/a	n/a
23	YY1	chr5:178986310-178986759	GM12878	blood:	n/a	chr5:178986551-178986559
24	STAT1	chr5:178986377-178986910	GM12878	blood:	n/a	n/a
25	TAF1	chr5:178986337-178986670	Hela-S3	cervix:	n/a	n/a
26	FOS	chr5:178985946-178986742	MCF10A-Er-Src	breast:	n/a	n/a
27	ELF1	chr5:178986353-178987142	GM12878	blood:	n/a	n/a
28	MYC	chr5:178985994-178986942	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr5:178986194-178987011	GM12892	blood:	n/a	n/a
30	SP4	chr5:178986008-178987045	H1-hESC	embryonic stem cell:	n/a	n/a
31	GABPA	chr5:178986379-178986939	A549	lung:	n/a	n/a
32	POLR2A	chr5:178985969-178987012	SK-N-MC	brain:	n/a	n/a
33	POLR2A	chr5:178986166-178987190	H1-neurons	neurons:	n/a	n/a
34	MYC	chr5:178985923-178987048	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr5:178986280-178986952	Hela-S3	cervix:	n/a	n/a
36	YY1	chr5:178986293-178986813	GM12878	blood:	n/a	chr5:178986551-178986559
37	WRNIP1	chr5:178986306-178986565	GM12878	blood:	n/a	n/a
38	POLR2A	chr5:178985826-178987315	SK-N-MC	brain:	n/a	n/a
39	ATF2	chr5:178985934-178986763	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr5:178985741-178987115	PANC-1	pancreas:	n/a	n/a
41	YY1	chr5:178985933-178986892	SK-N-SH	brain:	n/a	chr5:178986551-178986559
42	EP300	chr5:178986376-178986797	SK-N-SH_RA	brain:	n/a	n/a
43	YY1	chr5:178986228-178986836	A549	lung:	n/a	chr5:178986551-178986559
44	PML	chr5:178986339-178986641	GM12878	blood:	n/a	chr5:178986488-178986496
45	YY1	chr5:178985949-178986946	SK-N-SH_RA	brain:	n/a	chr5:178986551-178986559
46	POLR2A	chr5:178986007-178986911	GM12891	blood:	n/a	n/a
47	JUND	chr5:178985893-178986979	H1-hESC	embryonic stem cell:	n/a	n/a
48	SP1	chr5:178985918-178987320	HCT-116	colon:	n/a	chr5:178986611-178986625 chr5:178986510-178986519 chr5:178986509-178986518 chr5:178986510-178986519 chr5:178986616-178986625 chr5:178986615-178986624 chr5:178986614-178986626 chr5:178986614-178986626
49	POLR2A	chr5:178986199-178987194	HL-60	blood:	n/a	n/a
50	TAF1	chr5:178986259-178986913	PFSK-1	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178986412-178986462	HEEpiC	esophagus:	n/a
2	chr5:178986404-178986454	SKMC	muscle:	n/a
3	chr5:178986412-178986462	CMK	blood:	n/a
4	chr5:178986404-178986454	AG09319	gingival:	n/a
5	chr5:178986404-178986454	K562	blood:	n/a
6	chr5:178986404-178986454	A549	lung:	n/a
7	chr5:178986404-178986454	AG04449	skin:	fetal
8	chr5:178986404-178986454	HEEpiC	esophagus:	n/a
9	chr5:178986412-178986462	SK-N-SH_RA	brain:	n/a
10	chr5:178986412-178986462	HRE	kidney:	n/a
11	chr5:178986404-178986454	RPTEC	kidney:	n/a
12	chr5:178986412-178986462	SKMC	muscle:	n/a
13	chr5:178986404-178986454	GM19239	blood:	n/a
14	chr5:178986412-178986462	K562	blood:	n/a
15	chr5:178986404-178986454	SK-N-SH	brain:	n/a
16	chr5:178986412-178986462	Caco-2	colon:	n/a
17	chr5:178986404-178986454	HCF	heart:	n/a
18	chr5:178986412-178986462	GM12891	blood:	n/a
19	chr5:178986404-178986454	MCF10A-Er-Src	breast:	n/a
20	chr5:178986404-178986454	Hela-S3	cervix:	n/a
21	chr5:178986412-178986462	BJ	skin:	n/a
22	chr5:178986412-178986462	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:178986412-178986462	U87	brain:	n/a
24	chr5:178986412-178986462	HRCEpiC	kidney:	n/a
25	chr5:178986404-178986454	HRCEpiC	kidney:	n/a
26	chr5:178986404-178986454	HEK293	kidney:	embryo
27	chr5:178986412-178986462	HUVEC	blood vessel:	n/a
28	chr5:178986412-178986462	HRPEpiC	eye:	n/a
29	chr5:178986404-178986454	ProgFib	skin:	n/a
30	chr5:178986404-178986454	HRPEpiC	eye:	n/a
31	chr5:178986404-178986454	HMEC	breast:	n/a
32	chr5:178986412-178986462	SK-N-SH	brain:	n/a
33	chr5:178986404-178986454	HCPEpiC	choroid plexus:	n/a
34	chr5:178986404-178986454	AG04450	lung:	fetal
35	chr5:178986404-178986454	GM12892	blood:	n/a
36	chr5:178986404-178986454	SAEC	small airway:	n/a
37	chr5:178986404-178986454	GM12891	blood:	n/a
38	chr5:178986412-178986462	BE2_C	brain:	n/a
39	chr5:178986412-178986462	ECC-1	luminal epithelium:	n/a
40	chr5:178986412-178986462	HEK293	kidney:	embryo
41	chr5:178986404-178986454	ECC-1	luminal epithelium:	n/a
42	chr5:178986404-178986454	HUVEC	blood vessel:	n/a
43	chr5:178986404-178986454	AG10803	skin:	n/a
44	chr5:178986412-178986462	ProgFib	skin:	n/a
45	chr5:178986404-178986454	GM12878	blood:	n/a
46	chr5:178986412-178986462	IMR90	lung:	fetal
47	chr5:178986404-178986454	LNCaP	prostate:	n/a
48	chr5:178986404-178986454	SK-N-MC	brain:	n/a
49	chr5:178986412-178986462	GM19239	blood:	n/a
50	chr5:178986412-178986462	MCF10A-Er-Src	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178986094..178988194-chr5:179049451..179052935,4	MCF-7	breast:
2	chr5:178984878..178986642-chr5:178988155..178989998,2	MCF-7	breast:
3	chr5:177630883..177632521-chr5:178985029..178986804,2	MCF-7	breast:
4	chr5:178985235..178987908-chr5:179124412..179127341,2	MCF-7	breast:
5	chr5:178984205..178987569-chr5:178988108..178992792,6	MCF-7	breast:
6	chr5:178984896..178986468-chr5:179223868..179225684,2	MCF-7	breast:
7	chr5:178984558..178987542-chr5:178988263..178990973,3	K562	blood:
8	chr15:101835145..101835812-chr5:178986003..178986591,2	HCT-116	colon:
9	chr5:178966269..178968602-chr5:178984458..178986550,2	MCF-7	breast:
10	chr5:178984119..178986610-chr5:178999493..179002273,3	K562	blood:
11	chr5:178985192..178988541-chr5:179048594..179052191,5	MCF-7	breast:
12	chr5:178977809..178978321-chr5:178985908..178986661,2	MCF-7	breast:

No data

Variant related genes	Relation type
RUFY1	TF binding region
RUFY1	CpG island
ENSG00000131876	Chromatin interaction
ENSG00000197451	Chromatin interaction
ENSG00000127022	Chromatin interaction
ENSG00000259172	Chromatin interaction
ENSG00000169045	Chromatin interaction
ENSG00000176783	Chromatin interaction
ENSG00000221394	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 4 )

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

rs_ID	r²[population]
rs10064596	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10072757	0.80[CHD][hapmap]
rs10074573	1.00[CHB][hapmap];0.90[CHD][hapmap];0.96[MEX][hapmap];0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10078712	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10078796	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10479542	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12652495	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12658664	1.00[CEU][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13179470	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13183521	0.86[ASN][1000 genomes]
rs4131080	0.85[CEU][hapmap];0.80[GIH][hapmap];0.81[TSI][hapmap]
rs4376229	0.81[CEU][hapmap];0.80[GIH][hapmap]
rs4700835	0.88[ASN][1000 genomes]
rs4700836	0.88[ASN][1000 genomes]
rs4701130	1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4701131	1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4701132	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6601050	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6889447	0.85[CHB][hapmap]
rs6895321	0.81[ASN][1000 genomes]
rs6896112	0.88[ASN][1000 genomes]
rs6896940	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7703730	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7704349	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7718673	1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7723230	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7733389	0.95[CHB][hapmap];0.95[CHD][hapmap];0.84[ASN][1000 genomes]
rs7736163	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817413	chr5:178415365-179020558	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	esv2758031	chr5:178661266-179037529	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
3	esv2759397	chr5:178661266-179037529	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
4	nsv531996	chr5:178669297-178989687	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	esv2829850	chr5:178828854-179060995	Strong transcription Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases
6	nsv949554	chr5:178832325-179309513	Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	312 gene(s)	inside rSNPs	diseases
7	nsv1022509	chr5:178950829-179002751	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv883269	chr5:178951106-179031595	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
9	nsv883270	chr5:178951106-179350387	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	312 gene(s)	inside rSNPs	diseases
10	nsv1015477	chr5:178954409-179016804	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	nsv883271	chr5:178955046-179031595	Strong transcription Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv883272	chr5:178961872-179031595	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	nsv1028236	chr5:178962087-179019981	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs7702303	RUFY1	cis	parietal	SCAN
rs7702303	HNRPH1	Cis_1M	lymphoblastoid	RTeQTL
rs7702303	RUFY1	cis	cerebellum	SCAN
rs7702303	C5orf45	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178981200-178996200	Weak transcription	K562	blood
2	chr5:178985600-178986800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:178985600-178986800	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr5:178985600-178987000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr5:178985600-178987000	Active TSS	Brain Germinal Matrix	brain
6	chr5:178985600-178987000	Active TSS	HSMM	muscle
7	chr5:178985600-178987200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:178985600-178987400	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr5:178985600-178987400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr5:178985600-178987600	Active TSS	A549	lung
11	chr5:178985800-178986600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:178985800-178986800	Active TSS	Duodenum Mucosa	Duodenum
13	chr5:178985800-178986800	Active TSS	Rectal Smooth Muscle	rectum
14	chr5:178985800-178986800	Active TSS	HSMMtube	muscle
15	chr5:178985800-178986800	Active TSS	NH-A	brain
16	chr5:178985800-178987000	Active TSS	H1 Cell Line	embryonic stem cell
17	chr5:178985800-178987000	Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr5:178985800-178987000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:178985800-178987000	Active TSS	Brain Cingulate Gyrus	brain
20	chr5:178985800-178987000	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr5:178985800-178987000	Active TSS	Brain Substantia Nigra	brain
22	chr5:178985800-178987000	Active TSS	Duodenum Smooth Muscle	Duodenum
23	chr5:178985800-178987000	Active TSS	Fetal Lung	lung
24	chr5:178985800-178987000	Active TSS	Fetal Stomach	stomach
25	chr5:178985800-178987000	Active TSS	Right Atrium	heart
26	chr5:178985800-178987000	Active TSS	GM12878-XiMat	blood
27	chr5:178985800-178987000	Active TSS	NHDF-Ad	bronchial
28	chr5:178985800-178987000	Active TSS	NHLF	lung
29	chr5:178985800-178987200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr5:178985800-178987200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:178985800-178987200	Flanking Active TSS	Primary B cells from peripheral blood	blood
32	chr5:178985800-178987200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:178985800-178987200	Active TSS	Fetal Intestine Large	intestine
34	chr5:178985800-178987400	Active TSS	H9 Cell Line	embryonic stem cell
35	chr5:178985800-178987400	Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr5:178985800-178987400	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr5:178985800-178987400	Active TSS	Fetal Kidney	kidney
38	chr5:178985800-178987400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr5:178985800-178987400	Active TSS	HepG2	liver
40	chr5:178985800-178987600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:178986000-178986800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr5:178986000-178986800	Active TSS	Primary T helper cells PMA-I stimulated	--
43	chr5:178986000-178986800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
44	chr5:178986000-178986800	Active TSS	Pancreas	Pancrea
45	chr5:178986000-178986800	Active TSS	Psoas Muscle	Psoas
46	chr5:178986000-178986800	Active TSS	Right Ventricle	heart
47	chr5:178986000-178986800	Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr5:178986000-178986800	Active TSS	HMEC	breast
49	chr5:178986000-178987000	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr5:178986000-178987000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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