Variant report

Variant	rs3892337
Chromosome Location	chr13:53029485-53029486
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:406)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CREB1	chr13:53028961-53030175	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr13:53029318-53029794	A549	lung:	n/a	n/a
3	MXI1	chr13:53027965-53030679	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr13:53028515-53030244	Hela-S3	cervix:	n/a	n/a
5	RFX5	chr13:53028040-53030991	SK-N-SH	brain:	n/a	chr13:53029276-53029285 chr13:53029497-53029512 chr13:53029500-53029509 chr13:53029536-53029545
6	TAF1	chr13:53028998-53030236	H1-hESC	embryonic stem cell:	n/a	n/a
7	MAX	chr13:53028626-53030360	Hela-S3	cervix:	n/a	n/a
8	RFX5	chr13:53029029-53030101	GM12878	blood:	n/a	chr13:53029276-53029285 chr13:53029497-53029512 chr13:53029500-53029509 chr13:53029536-53029545
9	MXI1	chr13:53029074-53029595	H1-hESC	embryonic stem cell:	n/a	n/a
10	TBL1XR1	chr13:53029111-53030367	K562	blood:	n/a	n/a
11	POLR2A	chr13:53029150-53030213	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr13:53029110-53030261	PANC-1	pancreas:	n/a	n/a
13	E2F6	chr13:53029460-53030014	K562	blood:	n/a	chr13:53029650-53029665
14	TAF1	chr13:53029279-53030150	HepG2	liver:	n/a	n/a
15	CTCF	chr13:53029400-53029550	HBMEC	blood vessel:	n/a	n/a
16	YY1	chr13:53029226-53029679	K562	blood:	n/a	chr13:53029613-53029627 chr13:53029620-53029631
17	RAD21	chr13:53029344-53029651	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr13:53029132-53030478	HepG2	liver:	n/a	n/a
19	TAF1	chr13:53029208-53029840	MCF-7	breast:	n/a	n/a
20	USF2	chr13:53029043-53029575	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr13:53029004-53030173	K562	blood:	n/a	n/a
22	POLR2A	chr13:53029126-53030322	ECC-1	luminal epithelium:	n/a	n/a
23	TAF1	chr13:53029304-53029734	GM12892	blood:	n/a	n/a
24	CTCF	chr13:53029380-53029530	AG10803	skin:	n/a	n/a
25	IRF3	chr13:53029404-53029707	GM12878	blood:	n/a	chr13:53029567-53029581 chr13:53029517-53029531
26	EP300	chr13:53028380-53030182	GM12878	blood:	n/a	chr13:53029065-53029079 chr13:53028988-53029002
27	EP300	chr13:53029185-53030090	K562	blood:	n/a	n/a
28	POU2F2	chr13:53029004-53029731	GM12878	blood:	n/a	chr13:53029044-53029057
29	TAF1	chr13:53029441-53029630	A549	lung:	n/a	n/a
30	CREB1	chr13:53029057-53030204	A549	lung:	n/a	n/a
31	MXI1	chr13:53028647-53030036	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr13:53029046-53030080	GM12892	blood:	n/a	n/a
33	TBP	chr13:53029161-53030259	H1-hESC	embryonic stem cell:	n/a	n/a
34	HA-E2F1	chr13:53029421-53030129	Hela-S3	cervix:	n/a	chr13:53030075-53030084 chr13:53030108-53030117 chr13:53029650-53029665
35	STAT5A	chr13:53028650-53029495	GM12878	blood:	n/a	n/a
36	FOXP2	chr13:53029022-53029637	SK-N-MC	brain:	n/a	n/a
37	POLR2A	chr13:53029207-53030233	HepG2	liver:	n/a	n/a
38	ZBTB7A	chr13:53029445-53030361	ECC-1	luminal epithelium:	n/a	n/a
39	STAT1	chr13:53028630-53029767	GM12878	blood:	n/a	n/a
40	POLR2A	chr13:53029238-53030171	GM10847	blood:	n/a	n/a
41	ELF1	chr13:53029264-53029809	GM12878	blood:	n/a	n/a
42	POLR2A	chr13:53029152-53031480	K562	blood:	n/a	n/a
43	SP1	chr13:53028990-53030195	HCT-116	colon:	n/a	chr13:53030075-53030084 chr13:53029526-53029547 chr13:53030075-53030085 chr13:53030074-53030086 chr13:53030076-53030085 chr13:53030074-53030086 chr13:53029520-53029534 chr13:53030076-53030085 chr13:53029519-53029531 chr13:53030075-53030085 chr13:53029404-53029415 chr13:53030071-53030085 chr13:53029561-53029582
44	CTCF	chr13:53029095-53030375	K562	blood:	n/a	n/a
45	MAX	chr13:53028472-53030395	NB4	blood:	n/a	n/a
46	FOS	chr13:53029180-53029502	MCF10A-Er-Src	breast:	n/a	n/a
47	EP300	chr13:53029167-53029854	SK-N-SH_RA	brain:	n/a	n/a
48	ARID3A	chr13:53029122-53030383	HepG2	liver:	n/a	n/a
49	MYBL2	chr13:53029042-53030223	HepG2	liver:	n/a	n/a
50	TAF1	chr13:53029222-53029768	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:53029438-53029488	AG04450	lung:	fetal
2	chr13:53029438-53029488	HCM	heart:	n/a
3	chr13:53029438-53029488	MCF-7	breast:	n/a
4	chr13:53029438-53029488	AoSMC	blood vessel:	n/a
5	chr13:53029438-53029488	HepG2	liver:	n/a
6	chr13:53029438-53029488	Hela-S3	cervix:	n/a
7	chr13:53029438-53029488	SKMC	muscle:	n/a
8	chr13:53029438-53029488	Jurkat	blood:	n/a
9	chr13:53029438-53029488	BJ	skin:	n/a
10	chr13:53029438-53029488	NHDF-neo	bronchial:	n/a
11	chr13:53029438-53029488	HRCEpiC	kidney:	n/a
12	chr13:53029438-53029488	RPTEC	kidney:	n/a
13	chr13:53029438-53029488	IMR90	lung:	fetal
14	chr13:53029438-53029488	SK-N-MC	brain:	n/a
15	chr13:53029438-53029488	NT2-D1	testis:	n/a
16	chr13:53029438-53029488	HUVEC	blood vessel:	n/a
17	chr13:53029438-53029488	GM19239	blood:	n/a
18	chr13:53029438-53029488	GM06990	blood:	n/a
19	chr13:53029438-53029488	HCPEpiC	choroid plexus:	n/a
20	chr13:53029438-53029488	T-47D	breast:	n/a
21	chr13:53029438-53029488	A549	lung:	n/a
22	chr13:53029438-53029488	HPAEpiC	pulmonary alveolar:	n/a
23	chr13:53029438-53029488	HEEpiC	esophagus:	n/a
24	chr13:53029438-53029488	HAEpiC	amniotic membrane:	n/a
25	chr13:53029438-53029488	SK-N-SH	brain:	n/a
26	chr13:53029438-53029488	HL-60	blood:	n/a
27	chr13:53029438-53029488	ovcar-3	ovarian:	n/a
28	chr13:53029438-53029488	BE2_C	brain:	n/a
29	chr13:53029438-53029488	ProgFib	skin:	n/a
30	chr13:53029438-53029488	GM12891	blood:	n/a
31	chr13:53029438-53029488	K562	blood:	n/a
32	chr13:53029438-53029488	SAEC	small airway:	n/a
33	chr13:53029438-53029488	MCF10A-Er-Src	breast:	n/a
34	chr13:53029438-53029488	HIPEpiC	eye:	n/a
35	chr13:53029438-53029488	NHBE	bronchial:	n/a
36	chr13:53029438-53029488	GM12892	blood:	n/a
37	chr13:53029438-53029488	H1-hESC	embryonic stem cell:	embryo
38	chr13:53029438-53029488	U87	brain:	n/a
39	chr13:53029438-53029488	Hepatocyte	liver:	n/a
40	chr13:53029438-53029488	GM12878	blood:	n/a
41	chr13:53029438-53029488	ECC-1	luminal epithelium:	n/a
42	chr13:53029438-53029488	HRPEpiC	eye:	n/a
43	chr13:53029438-53029488	AG04449	skin:	fetal
44	chr13:53029438-53029488	Caco-2	colon:	n/a
45	chr13:53029438-53029488	LNCaP	prostate:	n/a
46	chr13:53029438-53029488	SK-N-SH_RA	brain:	n/a
47	chr13:53029438-53029488	HCF	heart:	n/a
48	chr13:53029438-53029488	CMK	blood:	n/a
49	chr13:53029438-53029488	PANC-1	pancreas:	n/a
50	chr13:53029438-53029488	PrEC	prostate:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:53344450..53346377-chr13:53029194..53030956,2	MCF-7	breast:
2	chr13:53029063..53030012-chrX:153718459..153719167,2	Hela-S3	cervix:
3	chr13:52989175..52991145-chr13:53028466..53031085,2	MCF-7	breast:
4	chr13:53029255..53030110-chr8:54934384..54934889,2	HCT-116	colon:
5	chr13:53028109..53029845-chr13:53190052..53193351,3	MCF-7	breast:
6	chr13:53029326..53030088-chr16:2204666..2205482,2	Hela-S3	cervix:
7	chr13:53023259..53027625-chr13:53027753..53030727,5	MCF-7	breast:
8	chr13:52377836..52379871-chr13:53028245..53029773,2	K562	blood:
9	chr13:52025134..52027888-chr13:53029090..53030597,2	MCF-7	breast:
10	chr1:155023406..155024318-chr13:53029329..53030119,2	NB4	blood:

No data

Variant related genes	Relation type
VPS36	TF binding region
CKAP2	TF binding region
CKAP2	CpG island
VPS36	CpG island
ENSG00000139675	Chromatin interaction
ENSG00000187735	Chromatin interaction
ENSG00000111057	Chromatin interaction
ENSG00000236778	Chromatin interaction
ENSG00000136100	Chromatin interaction
ENSG00000260260	Chromatin interaction
ENSG00000250299	Chromatin interaction
ENSG00000143537	Chromatin interaction
ENSG00000265039	Chromatin interaction
ENSG00000126903	Chromatin interaction
ENSG00000102786	Chromatin interaction
ENSG00000102796	Chromatin interaction
ENSG00000206630	Chromatin interaction
ENSG00000231856	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1056335	0.86[CHB][hapmap]
rs1057478	0.81[YRI][hapmap]
rs11148252	0.88[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11618716	0.88[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap];0.94[YRI][hapmap];0.82[EUR][1000 genomes]
rs11620062	0.89[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1327323	0.81[CHB][hapmap]
rs3803264	0.85[CHB][hapmap]
rs3886077	0.81[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.94[YRI][hapmap]
rs4286007	0.88[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs4884320	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs4884354	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs4884452	0.86[CHB][hapmap];0.84[JPT][hapmap];0.94[YRI][hapmap]
rs4885953	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs4886018	0.88[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap];0.94[YRI][hapmap];0.81[EUR][1000 genomes]
rs4886077	0.90[CHB][hapmap]
rs6561665	0.86[CHB][hapmap]
rs6561666	0.87[ASN][1000 genomes]
rs7321964	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7323666	0.90[CHB][hapmap]
rs7328653	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7333451	0.90[CHB][hapmap]
rs7334583	0.87[ASN][1000 genomes]
rs7336679	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs7987115	0.86[CHB][hapmap];0.84[JPT][hapmap];0.88[YRI][hapmap]
rs7990581	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7993748	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs8001624	0.90[CHB][hapmap]
rs9379	0.86[CHB][hapmap]
rs9526913	0.86[CHB][hapmap];0.84[JPT][hapmap];0.94[YRI][hapmap]
rs9526927	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9536046	0.86[CHB][hapmap]
rs9536048	0.86[CHB][hapmap]
rs9536052	0.86[CHB][hapmap]
rs9536066	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9536079	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9536220	0.82[YRI][hapmap]
rs9568732	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9568734	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9596643	0.84[CHB][hapmap]
rs9596648	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs9596649	0.87[ASN][1000 genomes]
rs9596651	0.86[CHB][hapmap];0.85[JPT][hapmap]

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	nsv934070	chr13:52362588-53174923	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv1040931	chr13:52564792-53350914	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv541773	chr13:52564792-53350914	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv428288	chr13:52728370-53068132	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv900084	chr13:52835231-53119704	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	esv1838257	chr13:52971893-53231454	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	esv3434605	chr13:52999509-53034851	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	n/a
8	nsv900085	chr13:53022518-53216622	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs3892337	CKAP2	cis	Muscle Skeletal	GTEx
rs3892337	CKAP2	cis	Artery Tibial	GTEx
rs3892337	CKAP2	cis	lung	GTEx
rs3892337	CKAP2	cis	Adipose Subcutaneous	GTEx
rs3892337	CKAP2	cis	Skin Sun Exposed Lower leg	GTEx
rs3892337	CKAP2	cis	Nerve Tibial	GTEx
rs3892337	CKAP2	cis	Thyroid	GTEx
rs3892337	CKAP2	cis	Heart Left Ventricle	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53028200-53030600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr13:53028200-53030800	Active TSS	Brain Angular Gyrus	brain
3	chr13:53028400-53030200	Active TSS	Brain Cingulate Gyrus	brain
4	chr13:53028400-53030400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr13:53028400-53030400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr13:53028400-53030400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr13:53028400-53030400	Active TSS	Brain Inferior Temporal Lobe	brain
8	chr13:53028400-53030400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr13:53028400-53030400	Active TSS	Rectal Smooth Muscle	rectum
10	chr13:53028400-53030400	Active TSS	NHDF-Ad	bronchial
11	chr13:53028400-53030600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr13:53028400-53030600	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr13:53028400-53030600	Active TSS	Colonic Mucosa	Colon
14	chr13:53028400-53030600	Active TSS	Fetal Intestine Large	intestine
15	chr13:53028400-53030600	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr13:53028400-53030600	Active TSS	K562	blood
17	chr13:53028400-53030800	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr13:53028400-53030800	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr13:53028400-53030800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr13:53028400-53030800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr13:53028400-53031000	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr13:53028400-53031600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr13:53028600-53030400	Active TSS	Esophagus	oesophagus
24	chr13:53028600-53030400	Active TSS	Fetal Heart	heart
25	chr13:53028600-53030400	Active TSS	Stomach Mucosa	stomach
26	chr13:53028600-53030600	Active TSS	H9 Cell Line	embryonic stem cell
27	chr13:53028600-53030600	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr13:53028600-53030600	Active TSS	Hela-S3	cervix
29	chr13:53028600-53031000	Active TSS	A549	lung
30	chr13:53028600-53033200	Active TSS	GM12878-XiMat	blood
31	chr13:53028800-53029600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr13:53028800-53030000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr13:53028800-53030200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr13:53028800-53030200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr13:53028800-53030200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr13:53028800-53030200	Active TSS	Primary B cells from peripheral blood	blood
37	chr13:53028800-53030200	Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr13:53028800-53030200	Active TSS	Gastric	stomach
39	chr13:53028800-53030400	Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr13:53028800-53030400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr13:53028800-53030400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr13:53028800-53030400	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr13:53028800-53030400	Active TSS	Muscle Satellite Cultured Cells	--
44	chr13:53028800-53030400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr13:53028800-53030400	Active TSS	Brain Substantia Nigra	brain
46	chr13:53028800-53030400	Active TSS	Duodenum Mucosa	Duodenum
47	chr13:53028800-53030400	Active TSS	Fetal Brain Female	brain
48	chr13:53028800-53030400	Active TSS	Pancreas	Pancrea
49	chr13:53028800-53030400	Active TSS	NHLF	lung
50	chr13:53028800-53030600	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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