Variant report

Variant	rs869951
Chromosome Location	chr13:95954210-95954211
allele	C/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	HA-E2F1	chr13:95953343-95954659	MCF-7	breast:	n/a	chr13:95954182-95954189 chr13:95953447-95953457 chr13:95953758-95953767 chr13:95954377-95954386 chr13:95954169-95954178
2	SIN3AK20	chr13:95952848-95954282	PANC-1	pancreas:	n/a	n/a
3	SP1	chr13:95953948-95954599	H1-hESC	embryonic stem cell:	n/a	chr13:95954169-95954178 chr13:95954168-95954177 chr13:95954377-95954386 chr13:95954378-95954387 chr13:95954167-95954179 chr13:95954167-95954179
4	E2F6	chr13:95953628-95954529	A549	lung:	n/a	chr13:95954182-95954189 chr13:95953758-95953767 chr13:95954377-95954386 chr13:95954169-95954178
5	RELA	chr13:95952790-95954553	GM15510	blood:	n/a	n/a
6	CTCF	chr13:95954120-95954270	AG10803	skin:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
7	POLR2A	chr13:95952711-95954360	U87	brain:	n/a	n/a
8	CTCF	chr13:95954060-95954210	HCM	heart:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
9	CTCF	chr13:95954120-95954270	HPAF	blood vessel:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
10	SMC3	chr13:95954079-95954383	K562	blood:	n/a	chr13:95954171-95954181
11	JUND	chr13:95953513-95954675	K562	blood:	n/a	n/a
12	PML	chr13:95953035-95954582	GM12878	blood:	n/a	n/a
13	POLR2A	chr13:95952769-95954393	GM12892	blood:	n/a	n/a
14	CTCF	chr13:95954140-95954290	HCPEpiC	choroid plexus:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
15	CTCF	chr13:95954060-95954210	HA-sp	spinal cord:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
16	MTA3	chr13:95953743-95954662	GM12878	blood:	n/a	n/a
17	CTCF	chr13:95954080-95954230	NHEK	skin:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
18	UBTF	chr13:95953061-95954252	K562	blood:	n/a	n/a
19	RUNX3	chr13:95952725-95954279	GM12878	blood:	n/a	n/a
20	RUNX3	chr13:95953649-95954301	GM12878	blood:	n/a	n/a
21	CTCF	chr13:95954140-95954290	AG09319	gingival:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
22	TBL1XR1	chr13:95953821-95954241	K562	blood:	n/a	n/a
23	MAX	chr13:95952783-95954619	HCT-116	colon:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
24	MYC	chr13:95952515-95954753	K562	blood:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
25	POLR2A	chr13:95952665-95954341	GM19099	blood:	n/a	n/a
26	BHLHE40	chr13:95954115-95954309	A549	lung:	n/a	n/a
27	CHD2	chr13:95952867-95954239	GM12878	blood:	n/a	chr13:95954182-95954189 chr13:95953205-95953215 chr13:95953384-95953394
28	CTCF	chr13:95954120-95954270	Caco-2	colon:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
29	CTCF	chr13:95954180-95954330	GM12873	blood:	n/a	n/a
30	MYC	chr13:95953599-95954621	K562	blood:	n/a	chr13:95953997-95954007 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
31	MAFK	chr13:95954131-95954685	K562	blood:	n/a	n/a
32	USF2	chr13:95953706-95954359	GM12878	blood:	n/a	chr13:95953784-95953800
33	CTCF	chr13:95953624-95954596	K562	blood:	n/a	chr13:95954171-95954184 chr13:95953788-95953801 chr13:95954172-95954182
34	CTCF	chr13:95954080-95954230	AG09319	gingival:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
35	UBTF	chr13:95952751-95954307	K562	blood:	n/a	n/a
36	CTCF	chr13:95954120-95954270	HEK293	kidney:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
37	TCF7L2	chr13:95952548-95954637	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr13:95953499-95954566	H1-hESC	embryonic stem cell:	n/a	n/a
39	MAX	chr13:95953741-95954381	MCF-7	breast:	n/a	chr13:95953997-95954007 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
40	USF1	chr13:95953748-95954235	ECC-1	luminal epithelium:	n/a	chr13:95953784-95953800
41	EP300	chr13:95953617-95954327	ECC-1	luminal epithelium:	n/a	chr13:95953707-95953723 chr13:95953714-95953730
42	E2F6	chr13:95953645-95954674	K562	blood:	n/a	chr13:95954182-95954189 chr13:95953758-95953767 chr13:95954377-95954386 chr13:95954169-95954178
43	GTF2F1	chr13:95953807-95954580	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr13:95952549-95954587	IMR90	lung:	n/a	n/a
45	TBL1XR1	chr13:95953779-95954681	GM12878	blood:	n/a	n/a
46	CTCF	chr13:95954140-95954290	HMEC	breast:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
47	MAX	chr13:95952614-95954650	A549	lung:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006
48	POLR2A	chr13:95953013-95954294	GM15510	blood:	n/a	n/a
49	CTCF	chr13:95954160-95954310	GM12864	blood:	n/a	chr13:95954171-95954184 chr13:95954172-95954182
50	MYC	chr13:95952716-95954293	Hela-S3	cervix:	n/a	chr13:95953361-95953370 chr13:95953997-95954007 chr13:95953361-95953368 chr13:95953759-95953769 chr13:95953815-95953822 chr13:95953999-95954006

Variant related genes	Relation type
ABCC4	TF binding region

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11843664	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12560549	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1764417	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1764419	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2992902	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2992903	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2992905	0.82[AMR][1000 genomes]
rs2992907	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2992908	0.82[AMR][1000 genomes]
rs2992909	0.82[AMR][1000 genomes]
rs2992910	0.82[AMR][1000 genomes]
rs2993579	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2993581	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2993582	0.82[AMR][1000 genomes]
rs2993583	0.82[AMR][1000 genomes]
rs2993584	0.82[AMR][1000 genomes]
rs2993585	0.82[AMR][1000 genomes]
rs61974974	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6650325	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8001444	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs871052	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9302056	0.82[AMR][1000 genomes]
rs9302058	0.82[AMR][1000 genomes]
rs9524895	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9524896	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533659	chr13:95757713-96042149	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1043019	chr13:95924585-96152616	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv900926	chr13:95927386-95972496	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv900927	chr13:95927386-95975185	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv456078	chr13:95929888-95972496	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv562770	chr13:95929888-95972496	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv900929	chr13:95930072-95972496	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv900930	chr13:95930072-95975185	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1037673	chr13:95930191-96146554	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv541882	chr13:95930191-96146554	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv900931	chr13:95930685-95972496	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1039391	chr13:95931369-96038728	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv471169	chr13:95931992-95972496	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv517610	chr13:95931992-96035883	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
15	nsv1047208	chr13:95935757-96036053	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv1044162	chr13:95936858-96032829	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	nsv1044131	chr13:95939874-96016445	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
18	nsv1040348	chr13:95939874-96032829	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv1042622	chr13:95939874-96038728	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
20	esv2829991	chr13:95942492-95981856	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	esv3693403	chr13:95942492-95981856	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
22	nsv456079	chr13:95942492-96027507	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
23	nsv562771	chr13:95942492-96027507	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
24	nsv1049988	chr13:95942492-96038728	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
25	nsv1036031	chr13:95943731-96030662	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
26	nsv1053262	chr13:95943731-96032829	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
27	nsv456080	chr13:95943885-96015129	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
28	nsv562772	chr13:95943885-96015129	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
29	nsv456081	chr13:95943885-96027507	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
30	nsv562773	chr13:95943885-96027507	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
31	nsv1047902	chr13:95945118-96032829	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
32	nsv562774	chr13:95951593-96027507	Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
33	esv3359395	chr13:95954035-95954389	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95950600-95954400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:95952000-95954600	Active TSS	A549	lung
3	chr13:95952400-95954400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr13:95952400-95954400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr13:95952400-95954400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr13:95952400-95954400	Active TSS	Brain Inferior Temporal Lobe	brain
7	chr13:95952400-95954400	Active TSS	NHDF-Ad	bronchial
8	chr13:95952400-95954600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr13:95952400-95954800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:95952400-95954800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:95952600-95954400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr13:95952600-95954400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
13	chr13:95952600-95954400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr13:95952600-95954400	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr13:95952600-95954400	Active TSS	Psoas Muscle	Psoas
16	chr13:95952600-95954400	Active TSS	HSMMtube	muscle
17	chr13:95952600-95954600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
18	chr13:95952600-95954600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
19	chr13:95952600-95954600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
20	chr13:95952600-95954600	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr13:95952600-95954600	Active TSS	Brain Anterior Caudate	brain
22	chr13:95952600-95954600	Active TSS	Brain Hippocampus Middle	brain
23	chr13:95952600-95954600	Active TSS	Fetal Brain Female	brain
24	chr13:95952600-95954600	Active TSS	Fetal Lung	lung
25	chr13:95952800-95954400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:95952800-95954400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr13:95952800-95954400	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr13:95952800-95954400	Active TSS	Aorta	Aorta
29	chr13:95952800-95954400	Active TSS	Fetal Heart	heart
30	chr13:95952800-95954400	Active TSS	Ovary	ovary
31	chr13:95952800-95954400	Active TSS	NHLF	lung
32	chr13:95952800-95954800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr13:95953000-95954400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr13:95953000-95954400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
35	chr13:95953000-95954400	Active TSS	Duodenum Smooth Muscle	Duodenum
36	chr13:95953000-95954600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
37	chr13:95953000-95954600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr13:95953000-95954600	Active TSS	Fetal Kidney	kidney
39	chr13:95953200-95954400	Flanking Active TSS	Colonic Mucosa	Colon
40	chr13:95953200-95954400	Active TSS	Esophagus	oesophagus
41	chr13:95953200-95954400	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr13:95953400-95954400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
43	chr13:95953400-95954400	Flanking Active TSS	Right Ventricle	heart
44	chr13:95953600-95954400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr13:95953800-95954400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr13:95953800-95954400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr13:95953800-95954400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
48	chr13:95953800-95954400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
49	chr13:95953800-95954400	Flanking Active TSS	Pancreas	Pancrea
50	chr13:95953800-95954400	Flanking Active TSS	HepG2	liver

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