Variant report

Variant	rs1886543
Chromosome Location	chr13:52701782-52701783
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:57)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:57 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr13:52701677-52702633	K562	blood:	n/a	n/a
2	RAD21	chr13:52701759-52702359	HepG2	liver:	n/a	n/a
3	RAD21	chr13:52701601-52702331	HepG2	liver:	n/a	n/a
4	RAD21	chr13:52701775-52702274	GM12878	blood:	n/a	n/a
5	SMC3	chr13:52701753-52702549	Hela-S3	cervix:	n/a	n/a
6	RAD21	chr13:52701715-52702282	Hela-S3	cervix:	n/a	n/a
7	RCOR1	chr13:52701579-52702218	K562	blood:	n/a	n/a
8	TEAD4	chr13:52701592-52702647	ECC-1	luminal epithelium:	n/a	n/a
9	STAT1	chr13:52701721-52702205	GM12878	blood:	n/a	n/a
10	MAX	chr13:52701725-52702724	HCT-116	colon:	n/a	n/a
11	MYC	chr13:52701629-52702611	K562	blood:	n/a	n/a
12	RAD21	chr13:52701700-52702287	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr13:52701769-52702266	MCF-7	breast:	n/a	n/a
14	TAL1	chr13:52701711-52702122	K562	blood:	n/a	n/a
15	CTCF	chr13:52701686-52702412	HCT-116	colon:	n/a	n/a
16	MAFK	chr13:52701566-52702107	HepG2	liver:	n/a	chr13:52701700-52701711 chr13:52701698-52701712
17	ARID3A	chr13:52701599-52702201	K562	blood:	n/a	n/a
18	MAX	chr13:52701775-52702734	ECC-1	luminal epithelium:	n/a	n/a
19	ZMIZ1	chr13:52701646-52702126	K562	blood:	n/a	n/a
20	TEAD4	chr13:52701776-52702284	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr13:52701755-52702186	A549	lung:	n/a	n/a
22	CBX3	chr13:52701679-52702219	K562	blood:	n/a	n/a
23	RAD21	chr13:52701761-52702362	A549	lung:	n/a	n/a
24	MAX	chr13:52701670-52703501	ECC-1	luminal epithelium:	n/a	chr13:52702985-52702994
25	MAFF	chr13:52701525-52702302	K562	blood:	n/a	chr13:52701697-52701715
26	CTCF	chr13:52701660-52701810	BJ	skin:	n/a	n/a
27	RAD21	chr13:52701742-52702332	H1-hESC	embryonic stem cell:	n/a	n/a
28	RAD21	chr13:52701576-52702378	ECC-1	luminal epithelium:	n/a	n/a
29	CTCF	chr13:52701659-52702304	K562	blood:	n/a	n/a
30	MAFK	chr13:52701580-52702139	IMR90	lung:	n/a	chr13:52701700-52701711 chr13:52701698-52701712
31	RAD21	chr13:52701623-52702285	H1-hESC	embryonic stem cell:	n/a	n/a
32	RAD21	chr13:52701673-52702265	K562	blood:	n/a	n/a
33	SMC3	chr13:52701764-52702400	GM12878	blood:	n/a	n/a
34	RAD21	chr13:52701734-52702444	HCT-116	colon:	n/a	n/a
35	TBL1XR1	chr13:52701660-52702207	K562	blood:	n/a	n/a
36	MAZ	chr13:52701717-52703491	IMR90	lung:	n/a	chr13:52702985-52702994
37	MXI1	chr13:52701549-52703476	IMR90	lung:	n/a	chr13:52702985-52703000 chr13:52702983-52702998
38	TEAD4	chr13:52701773-52702582	ECC-1	luminal epithelium:	n/a	n/a
39	JUND	chr13:52701659-52702507	K562	blood:	n/a	n/a
40	RAD21	chr13:52701361-52703701	SK-N-SH	brain:	n/a	chr13:52702753-52702767 chr13:52702727-52702737
41	SMC3	chr13:52701650-52702300	HepG2	liver:	n/a	n/a
42	CTCF	chr13:52701768-52702209	HepG2	liver:	n/a	n/a
43	CTCF	chr13:52701596-52703641	SK-N-SH	brain:	n/a	n/a
44	JUN	chr13:52701495-52702126	K562	blood:	n/a	n/a
45	RAD21	chr13:52701782-52702330	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr13:52701478-52702675	A549	lung:	n/a	n/a
47	RAD21	chr13:52701657-52702358	ECC-1	luminal epithelium:	n/a	n/a
48	MAFK	chr13:52701537-52702096	HepG2	liver:	n/a	chr13:52701700-52701711 chr13:52701698-52701712
49	RAD21	chr13:52701742-52702288	MCF-7	breast:	n/a	n/a
50	TEAD4	chr13:52701774-52702489	K562	blood:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:52701771..52705558-chr13:52767896..52769871,3	MCF-7	breast:
2	chr13:52376169..52378547-chr13:52701514..52703656,2	MCF-7	breast:
3	chr13:52600318..52601043-chr13:52701669..52702499,2	MCF-7	breast:
4	chr13:52578352..52579378-chr13:52701728..52702446,3	MCF-7	breast:
5	chr13:52584477..52586943-chr13:52701489..52703372,3	K562	blood:
6	chr13:52486050..52486951-chr13:52701619..52702125,2	MCF-7	breast:
7	chr13:52509591..52510539-chr13:52701676..52702543,4	MCF-7	breast:
8	chr13:52584477..52586900-chr13:52700506..52703372,3	K562	blood:
9	chr13:52388965..52389862-chr13:52701684..52702477,3	K562	blood:

No data

Variant related genes	Relation type
NEK5	TF binding region
ENSG00000253710	Chromatin interaction
ENSG00000102796	Chromatin interaction
ENSG00000231856	Chromatin interaction
ENSG00000243406	Chromatin interaction
ENSG00000123191	Chromatin interaction

Extended variants
information (count: 129 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:122)

rs_ID	r²[population]
rs1004576	0.93[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.92[MKK][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1055062	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1060631	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1134727	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11620583	0.87[CHB][hapmap]
rs12146904	1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.87[MKK][hapmap];1.00[ASN][1000 genomes]
rs12431310	1.00[CHB][hapmap];0.95[JPT][hapmap];0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12560598	0.90[ASN][1000 genomes]
rs1327323	0.87[MEX][hapmap]
rs1571189	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1801243	0.91[CHB][hapmap]
rs1886538	0.91[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap]
rs1886539	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1886542	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs1886544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1886545	0.91[ASN][1000 genomes]
rs1886546	0.90[ASN][1000 genomes]
rs1886547	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs1924611	0.86[CHB][hapmap]
rs2004866	0.91[CHB][hapmap]
rs2005182	0.97[ASN][1000 genomes]
rs2181891	0.91[CHB][hapmap]
rs2274202	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs2277448	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs2296347	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2296348	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs2296349	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs2408544	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs2408546	0.94[ASN][1000 genomes]
rs2408547	0.95[ASN][1000 genomes]
rs2408548	0.95[ASN][1000 genomes]
rs2408550	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs2408551	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs2408552	1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.90[LWK][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2408554	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2408609	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs2408611	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs2897964	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2897965	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2897977	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs3368	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs3742289	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3742291	0.90[ASN][1000 genomes]
rs3783242	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3818422	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3825528	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs4261421	0.94[ASN][1000 genomes]
rs4264295	0.94[ASN][1000 genomes]
rs4297592	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs4497567	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs4941727	0.81[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.89[LWK][hapmap];0.91[MEX][hapmap];0.85[YRI][hapmap];0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4943060	0.89[ASN][1000 genomes]
rs61958804	0.91[ASN][1000 genomes]
rs61958805	0.88[ASN][1000 genomes]
rs6561656	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6561658	0.81[CEU][hapmap];0.86[CHB][hapmap];0.80[JPT][hapmap]
rs6650384	0.95[ASN][1000 genomes]
rs6650385	0.95[ASN][1000 genomes]
rs66849828	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7318287	0.94[ASN][1000 genomes]
rs7319784	0.88[ASN][1000 genomes]
rs7320252	0.95[ASN][1000 genomes]
rs7320429	0.95[ASN][1000 genomes]
rs732071	0.91[CHB][hapmap];0.93[CHD][hapmap];0.90[JPT][hapmap]
rs7320831	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7321120	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7321310	0.88[ASN][1000 genomes]
rs7321435	0.91[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap]
rs7324458	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7327634	0.91[CHB][hapmap]
rs7332356	0.90[ASN][1000 genomes]
rs7338131	0.95[ASN][1000 genomes]
rs747781	0.91[CHB][hapmap]
rs755363	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7981050	0.87[MEX][hapmap]
rs7981904	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs7991237	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7995946	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7998770	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs9316563	0.87[CHB][hapmap]
rs9526819	0.87[CHB][hapmap]
rs9526823	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs9526825	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9526826	0.95[ASN][1000 genomes]
rs9526834	0.96[ASN][1000 genomes]
rs9526835	0.94[ASN][1000 genomes]
rs9526836	1.00[ASN][1000 genomes]
rs9526837	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9526841	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9526842	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs9526843	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9535812	0.91[CHB][hapmap]
rs9535822	0.86[CHB][hapmap]
rs9535825	0.91[CHB][hapmap];0.91[CHD][hapmap];0.85[JPT][hapmap]
rs9535826	0.87[CHB][hapmap]
rs9535832	0.91[CHB][hapmap]
rs9535836	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535845	0.95[ASN][1000 genomes]
rs9535851	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535853	0.90[ASN][1000 genomes]
rs9535856	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535858	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535861	0.91[CHB][hapmap];0.85[CHD][hapmap];0.85[JPT][hapmap];0.87[LWK][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs9535862	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535866	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535867	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9535871	0.95[ASN][1000 genomes]
rs9535873	0.93[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.90[MKK][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9535878	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535879	0.90[CHB][hapmap];0.84[JPT][hapmap]
rs9535880	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535882	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535883	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9535885	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs9535887	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9535888	0.85[ASN][1000 genomes]
rs9535889	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9563089	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9568682	0.91[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap]
rs9568684	0.89[JPT][hapmap]
rs9568692	0.95[ASN][1000 genomes]
rs9568713	0.91[CHB][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530718	chr13:52291802-52832752	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers 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	38 gene(s)	inside rSNPs	diseases
2	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
3	nsv900082	chr13:52555288-52709938	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	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
5	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
6	nsv1037567	chr13:52643647-52802799	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	esv3429935	chr13:52694751-52735744	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs1886543	NEK3	cis	normal skin	skin_eQTL
rs1886543	LOC440138	cis	multi-tissue	Pritchard
rs1886543	NEK3	cis	Adipose Subcutaneous	GTEx
rs1886543	CKAP2	cis	multi-tissue	Pritchard
rs1886543	NEK3	cis	Muscle Skeletal	GTEx
rs1886543	ATP7B	cis	cerebellum	SCAN
rs1886543	VPS36	cis	cerebellum	SCAN
rs1886543	CKAP2	cis	parietal	SCAN
rs1886543	CKAP2	cis	cerebellum	SCAN
rs1886543	LECT1	cis	parietal	SCAN

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52699000-52701800	Enhancers	K562	blood
2	chr13:52701000-52701800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr13:52701200-52701800	Enhancers	Fetal Intestine Small	intestine
4	chr13:52701400-52701800	Enhancers	NHEK	skin
5	chr13:52701600-52701800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:52701600-52701800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr13:52701600-52701800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr13:52701600-52701800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr13:52701600-52701800	Enhancers	Brain Cingulate Gyrus	brain
10	chr13:52701600-52701800	Active TSS	Colon Smooth Muscle	Colon
11	chr13:52701600-52701800	Enhancers	Duodenum Mucosa	Duodenum
12	chr13:52701600-52701800	Enhancers	Fetal Heart	heart
13	chr13:52701600-52701800	Enhancers	Fetal Kidney	kidney
14	chr13:52701600-52701800	Enhancers	Rectal Smooth Muscle	rectum
15	chr13:52701600-52701800	Enhancers	Stomach Mucosa	stomach
16	chr13:52701600-52701800	Enhancers	HepG2	liver
17	chr13:52701600-52702000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr13:52701600-52702000	Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr13:52701600-52702000	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr13:52701600-52702000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr13:52701600-52702000	Enhancers	Adipose Nuclei	Adipose
22	chr13:52701600-52702000	Enhancers	Colonic Mucosa	Colon
23	chr13:52701600-52702000	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr13:52701600-52702000	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr13:52701600-52702200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr13:52701600-52702200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr13:52701600-52702200	Enhancers	Fetal Stomach	stomach
28	chr13:52701600-52702200	Flanking Active TSS	Stomach Smooth Muscle	stomach
29	chr13:52701600-52702200	Enhancers	HMEC	breast
30	chr13:52701600-52702200	Enhancers	HSMMtube	muscle

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