Variant report

Variant	rs2181891
Chromosome Location	chr13:52553358-52553359
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:90)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:90 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr13:52552903-52553484	K562	blood:	n/a	n/a
2	ATF3	chr13:52553156-52553449	K562	blood:	n/a	n/a
3	HEY1	chr13:52552946-52553399	K562	blood:	n/a	n/a
4	MAX	chr13:52552954-52553399	K562	blood:	n/a	n/a
5	EP300	chr13:52553045-52553532	HepG2	liver:	n/a	n/a
6	EP300	chr13:52552907-52553431	K562	blood:	n/a	n/a
7	USF1	chr13:52553190-52553463	H1-hESC	embryonic stem cell:	n/a	n/a
8	RCOR1	chr13:52552886-52553450	K562	blood:	n/a	n/a
9	HNF4A	chr13:52553048-52553492	HepG2	liver:	n/a	chr13:52553245-52553260
10	CEBPD	chr13:52553057-52553384	HepG2	liver:	n/a	n/a
11	USF2	chr13:52553180-52553461	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr13:52553116-52553463	K562	blood:	n/a	n/a
13	CEBPB	chr13:52553183-52553459	HCT-116	colon:	n/a	chr13:52553277-52553288
14	HEY1	chr13:52553115-52553534	HepG2	liver:	n/a	n/a
15	ATF1	chr13:52552888-52553465	K562	blood:	n/a	n/a
16	JUND	chr13:52552975-52553469	K562	blood:	n/a	n/a
17	ZNF143	chr13:52552997-52553376	K562	blood:	n/a	n/a
18	SMC3	chr13:52553077-52553438	HepG2	liver:	n/a	n/a
19	ATF3	chr13:52553100-52553433	K562	blood:	n/a	n/a
20	CBX3	chr13:52552933-52553521	K562	blood:	n/a	n/a
21	CEBPD	chr13:52553054-52553409	HepG2	liver:	n/a	n/a
22	SP1	chr13:52553004-52553558	HepG2	liver:	n/a	n/a
23	MAX	chr13:52553136-52553497	HepG2	liver:	n/a	n/a
24	MAX	chr13:52552937-52553591	HepG2	liver:	n/a	n/a
25	FOXA1	chr13:52552991-52553489	HepG2	liver:	n/a	n/a
26	USF1	chr13:52552920-52553507	K562	blood:	n/a	n/a
27	MYC	chr13:52552844-52553419	K562	blood:	n/a	n/a
28	ATF3	chr13:52553234-52553408	HepG2	liver:	n/a	n/a
29	NFYB	chr13:52553086-52553489	K562	blood:	n/a	n/a
30	USF2	chr13:52553121-52553510	K562	blood:	n/a	n/a
31	HDAC2	chr13:52553039-52553413	HepG2	liver:	n/a	n/a
32	MAX	chr13:52553136-52553453	NB4	blood:	n/a	n/a
33	JUND	chr13:52553138-52553433	HepG2	liver:	n/a	n/a
34	FOXA1	chr13:52553116-52553518	HepG2	liver:	n/a	n/a
35	IRF1	chr13:52553116-52553564	K562	blood:	n/a	n/a
36	ARID3A	chr13:52553095-52553479	HepG2	liver:	n/a	n/a
37	USF1	chr13:52553065-52553559	HCT-116	colon:	n/a	n/a
38	CEBPB	chr13:52553146-52553376	MCF-7	breast:	n/a	chr13:52553277-52553288
39	CEBPB	chr13:52552875-52553551	K562	blood:	n/a	chr13:52553277-52553288
40	CEBPB	chr13:52553182-52553416	H1-hESC	embryonic stem cell:	n/a	chr13:52553277-52553288
41	USF1	chr13:52553184-52553394	SK-N-SH_RA	brain:	n/a	n/a
42	ARID3A	chr13:52553083-52553442	K562	blood:	n/a	n/a
43	CEBPB	chr13:52553016-52553495	HepG2	liver:	n/a	chr13:52553277-52553288
44	USF1	chr13:52553236-52553415	SK-N-SH_RA	brain:	n/a	n/a
45	TAL1	chr13:52552984-52553413	K562	blood:	n/a	n/a
46	CEBPB	chr13:52553148-52553409	Hela-S3	cervix:	n/a	chr13:52553277-52553288
47	CREB1	chr13:52552965-52553576	HepG2	liver:	n/a	n/a
48	CEBPB	chr13:52553126-52553428	HepG2	liver:	n/a	chr13:52553277-52553288
49	MAX	chr13:52552899-52553459	K562	blood:	n/a	n/a
50	USF1	chr13:52553194-52553507	ECC-1	luminal epithelium:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:52547935..52549465-chr13:52552409..52555264,2	K562	blood:
2	chr13:52549808..52551859-chr13:52553072..52555669,2	K562	blood:

No data

Variant related genes	Relation type
ATP7B	TF binding region
ENSG00000123191	Chromatin interaction

Extended variants
information (count: 121 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs1004576	0.91[CHB][hapmap]
rs1051332	0.82[GIH][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs1055062	0.91[CHB][hapmap]
rs1060631	0.91[CHB][hapmap]
rs11616964	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11620583	0.89[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12146904	0.91[CHB][hapmap]
rs12431310	0.91[CHB][hapmap]
rs1571189	0.91[CHB][hapmap];0.80[JPT][hapmap]
rs1801243	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1801244	0.96[CEU][hapmap];0.84[CHD][hapmap];0.87[GIH][hapmap];0.83[MEX][hapmap];0.86[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1886538	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs1886542	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs1886543	0.91[CHB][hapmap]
rs1886544	0.91[CHB][hapmap]
rs1886547	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap]
rs1924611	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1951922	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2004866	0.89[CEU][hapmap];0.81[CHB][hapmap];0.88[GIH][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2104353	0.80[EUR][1000 genomes]
rs2147363	0.82[CHD][hapmap]
rs2274202	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2277448	0.91[CHB][hapmap]
rs2296246	0.81[CEU][hapmap];0.82[GIH][hapmap];0.82[TSI][hapmap];0.82[EUR][1000 genomes]
rs2296347	0.91[CHB][hapmap]
rs2296348	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2296349	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2408544	0.89[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes]
rs2408550	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap]
rs2408551	0.82[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap]
rs2408552	0.91[CHB][hapmap];0.80[JPT][hapmap]
rs2408554	0.91[CHB][hapmap]
rs2408609	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2408611	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2897964	0.91[CHB][hapmap]
rs2897977	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs3368	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs3742288	0.96[CEU][hapmap];0.87[CHD][hapmap];0.90[GIH][hapmap];0.87[MEX][hapmap];0.85[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3742289	0.91[CHB][hapmap]
rs3783241	0.82[EUR][1000 genomes]
rs3783242	0.91[CHB][hapmap]
rs3818422	0.91[CHB][hapmap]
rs3825526	0.81[CEU][hapmap];0.82[GIH][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs3825527	0.96[CEU][hapmap];0.87[CHD][hapmap];0.92[GIH][hapmap];0.84[MEX][hapmap];0.85[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3825528	0.89[CEU][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap];0.86[AMR][1000 genomes]
rs4297592	0.85[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap]
rs4497567	0.91[CHB][hapmap]
rs4941727	0.91[CHB][hapmap];0.80[JPT][hapmap]
rs6561656	0.91[CHB][hapmap]
rs723102	0.81[AMR][1000 genomes]
rs723103	0.81[AMR][1000 genomes]
rs732071	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs7320831	0.91[CHB][hapmap]
rs7321120	0.91[CHB][hapmap]
rs7321435	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs7324458	0.91[CHB][hapmap]
rs7327634	0.89[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.81[JPT][hapmap];0.87[MEX][hapmap];0.85[AMR][1000 genomes]
rs747781	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.88[YRI][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs750290	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs752570	0.81[EUR][1000 genomes]
rs754610	0.81[CEU][hapmap];0.82[GIH][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs755363	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap]
rs7981904	0.91[CHB][hapmap];0.80[JPT][hapmap]
rs7991237	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap]
rs7994928	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7995946	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.84[MEX][hapmap]
rs7998770	0.91[CHB][hapmap]
rs7999812	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9316563	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9526811	0.82[EUR][1000 genomes]
rs9526812	0.81[CEU][hapmap];0.82[GIH][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs9526814	0.85[CEU][hapmap];0.82[GIH][hapmap];0.87[TSI][hapmap];0.83[EUR][1000 genomes]
rs9526819	0.89[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9526821	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9526823	0.91[CHB][hapmap]
rs9526825	0.91[CHB][hapmap]
rs9526837	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap]
rs9526841	0.91[CHB][hapmap]
rs9526842	0.86[JPT][hapmap]
rs9535797	0.81[EUR][1000 genomes]
rs9535812	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9535817	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9535819	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9535822	0.89[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9535823	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9535825	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs9535826	0.89[CEU][hapmap];0.95[CHB][hapmap];0.88[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9535828	0.89[CEU][hapmap];0.96[MEX][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9535829	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9535832	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs9535833	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9535836	0.89[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap];0.85[AMR][1000 genomes]
rs9535851	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap]
rs9535856	0.81[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap]
rs9535858	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap]
rs9535861	0.82[CHB][hapmap]
rs9535862	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap]
rs9535866	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.87[MEX][hapmap]
rs9535867	0.91[CHB][hapmap]
rs9535873	0.91[CHB][hapmap]
rs9535878	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs9535879	0.80[CHB][hapmap];0.84[JPT][hapmap]
rs9535880	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs9535882	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs9535885	0.86[JPT][hapmap]
rs9535887	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs9563084	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9563089	0.89[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap];0.86[AMR][1000 genomes]
rs9568677	0.81[CEU][hapmap];0.82[GIH][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs9568681	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9568682	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs9568684	0.86[CHB][hapmap];0.89[JPT][hapmap]
rs9568713	0.85[CEU][hapmap];0.81[CHB][hapmap];0.85[GIH][hapmap];0.86[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	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	nsv1044310	chr13:52321564-52643924	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1050117	chr13:52325116-52643924	Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	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
5	nsv455888	chr13:52491193-52570728	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv561649	chr13:52491193-52570728	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv1041996	chr13:52544805-52581501	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a
8	esv2763022	chr13:52544978-52581513	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs2181891	LOC440138	cis	multi-tissue	Pritchard
rs2181891	ALG11	cis	Artery Tibial	GTEx
rs2181891	NCRNA00282	cis	cerebellum	SCAN
rs2181891	CKAP2	cis	parietal	SCAN
rs2181891	CKAP2	cis	cerebellum	SCAN
rs2181891	CKAP2	cis	multi-tissue	Pritchard

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52494400-52558000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:52513400-52555400	Weak transcription	Brain Hippocampus Middle	brain
3	chr13:52516600-52554000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr13:52516800-52555400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr13:52530200-52555400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr13:52534400-52555400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr13:52540000-52554600	Weak transcription	HSMMtube	muscle
8	chr13:52541400-52554800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr13:52544800-52554400	Weak transcription	Brain Anterior Caudate	brain
10	chr13:52544800-52556600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:52545000-52555400	Weak transcription	Adipose Nuclei	Adipose
12	chr13:52545000-52555600	Weak transcription	Aorta	Aorta
13	chr13:52545400-52555400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:52549000-52555400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr13:52549000-52555600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr13:52550200-52554200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr13:52551600-52555800	Enhancers	Fetal Intestine Small	intestine
18	chr13:52551800-52554800	Enhancers	Fetal Heart	heart
19	chr13:52552600-52553600	Flanking Active TSS	K562	blood
20	chr13:52552600-52554400	Enhancers	Fetal Intestine Large	intestine
21	chr13:52552600-52555800	Enhancers	Stomach Mucosa	stomach
22	chr13:52552800-52553400	Enhancers	Duodenum Mucosa	Duodenum
23	chr13:52552800-52553400	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr13:52553000-52553400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr13:52553000-52553400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr13:52553000-52553400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr13:52553000-52553400	Enhancers	Placenta	Placenta
28	chr13:52553000-52553400	Enhancers	Left Ventricle	heart
29	chr13:52553000-52553400	Enhancers	Ovary	ovary
30	chr13:52553000-52553400	Enhancers	Pancreas	Pancrea
31	chr13:52553000-52553400	Enhancers	Psoas Muscle	Psoas
32	chr13:52553000-52553400	Enhancers	Right Atrium	heart
33	chr13:52553000-52553400	Enhancers	Right Ventricle	heart
34	chr13:52553000-52553600	Flanking Active TSS	Liver	Liver
35	chr13:52553000-52555800	Enhancers	Fetal Lung	lung
36	chr13:52553200-52556800	Enhancers	HepG2	liver

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