Variant report

Variant	rs71456309
Chromosome Location	chr11:64108262-64108263
allele	G/T
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	POLR2A	chr11:64107291-64108469	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:64107343-64108445	GM12892	blood:	n/a	n/a
3	POLR2A	chr11:64107266-64108404	GM12891	blood:	n/a	n/a
4	PML	chr11:64107081-64108570	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:64107178-64108434	GM12892	blood:	n/a	n/a
6	SPI1	chr11:64108048-64108332	GM12878	blood:	n/a	n/a
7	MAZ	chr11:64107154-64108557	GM12878	blood:	n/a	chr11:64107865-64107875 chr11:64108303-64108313
8	POLR2A	chr11:64108052-64108613	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr11:64107414-64108812	HL-60	blood:	n/a	n/a
10	POLR2A	chr11:64106838-64108401	GM19099	blood:	n/a	n/a
11	SP4	chr11:64108096-64108868	H1-hESC	embryonic stem cell:	n/a	chr11:64108507-64108518 chr11:64108300-64108316 chr11:64108298-64108314 chr11:64108279-64108295
12	POLR2A	chr11:64107316-64108393	GM12878	blood:	n/a	n/a
13	SP1	chr11:64108036-64108956	H1-hESC	embryonic stem cell:	n/a	chr11:64108281-64108293 chr11:64108702-64108711 chr11:64108281-64108293 chr11:64108303-64108313 chr11:64108302-64108314 chr11:64108702-64108711 chr11:64108303-64108313 chr11:64108507-64108518 chr11:64108302-64108314 chr11:64108703-64108712 chr11:64108303-64108312 chr11:64108304-64108313
14	POLR2A	chr11:64106936-64108469	GM12878	blood:	n/a	n/a
15	POLR2A	chr11:64107062-64108493	GM12878	blood:	n/a	n/a
16	POLR2A	chr11:64106788-64108606	GM12892	blood:	n/a	n/a
17	POLR2A	chr11:64107047-64108499	Raji	blood:	n/a	n/a
18	TAF1	chr11:64108066-64108278	GM12892	blood:	n/a	n/a
19	NRF1	chr11:64108170-64108266	GM12878	blood:	n/a	n/a
20	EBF1	chr11:64108259-64108539	GM12878	blood:	n/a	n/a
21	POLR2A	chr11:64107349-64108777	HL-60	blood:	n/a	n/a
22	EP300	chr11:64108123-64108266	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:64107989-64108471	PBDE	blood:	n/a	n/a
24	HMGN3	chr11:64108250-64108530	K562	blood:	n/a	n/a
25	POLR2A	chr11:64107948-64108360	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:64107350-64108413	GM18526	blood:	n/a	n/a
27	SP1	chr11:64108075-64108523	GM12878	blood:	n/a	chr11:64108281-64108293 chr11:64108281-64108293 chr11:64108303-64108313 chr11:64108302-64108314 chr11:64108303-64108313 chr11:64108507-64108518 chr11:64108302-64108314 chr11:64108303-64108312 chr11:64108304-64108313
28	JUND	chr11:64108218-64108743	H1-hESC	embryonic stem cell:	n/a	chr11:64108343-64108352
29	CHD1	chr11:64107310-64108304	GM12878	blood:	n/a	n/a
30	SIN3A	chr11:64108254-64108284	GM12878	blood:	n/a	n/a
31	ELF1	chr11:64107144-64108941	GM12878	blood:	n/a	chr11:64107675-64107688 chr11:64107677-64107688 chr11:64107862-64107874
32	TBP	chr11:64108101-64108528	GM12878	blood:	n/a	chr11:64108262-64108273
33	RUNX3	chr11:64107053-64108551	GM12878	blood:	n/a	n/a
34	POLR2A	chr11:64106985-64108487	GM12891	blood:	n/a	n/a
35	IRF1	chr11:64108190-64108539	K562	blood:	n/a	chr11:64108302-64108316 chr11:64108281-64108295 chr11:64108343-64108357
36	TAF1	chr11:64108077-64108269	GM12878	blood:	n/a	n/a
37	POLR2A	chr11:64107385-64108444	GM12878	blood:	n/a	n/a
38	EBF1	chr11:64107153-64108440	GM12878	blood:	n/a	n/a
39	TBP	chr11:64108181-64108712	H1-hESC	embryonic stem cell:	n/a	chr11:64108262-64108273
40	POLR2A	chr11:64107277-64108500	GM12878	blood:	n/a	n/a
41	ZNF143	chr11:64108142-64108465	GM12878	blood:	n/a	n/a
42	ZBTB7A	chr11:64108218-64108774	K562	blood:	n/a	n/a
43	SP4	chr11:64108165-64108836	H1-hESC	embryonic stem cell:	n/a	chr11:64108507-64108518 chr11:64108300-64108316 chr11:64108298-64108314 chr11:64108279-64108295
44	STAT1	chr11:64108134-64108347	GM12878	blood:	n/a	n/a
45	POLR2A	chr11:64106744-64108657	GM12878	blood:	n/a	n/a
46	POU2F2	chr11:64108012-64108438	GM12878	blood:	n/a	n/a
47	MAZ	chr11:64108187-64108822	K562	blood:	n/a	chr11:64108303-64108313
48	TAF1	chr11:64108058-64108384	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr11:64108148-64108825	K562	blood:	n/a	n/a
50	MTA3	chr11:64106840-64108780	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64108241-64108291	HEEpiC	esophagus:	n/a
2	chr11:64108241-64108291	GM12892	blood:	n/a
3	chr11:64108241-64108291	NHBE	bronchial:	n/a
4	chr11:64108241-64108291	HRCEpiC	kidney:	n/a
5	chr11:64108241-64108291	SK-N-MC	brain:	n/a
6	chr11:64108241-64108291	AG09309	skin:	n/a
7	chr11:64108241-64108291	NH-A	brain:	n/a
8	chr11:64108241-64108291	SKMC	muscle:	n/a
9	chr11:64108241-64108291	RPTEC	kidney:	n/a
10	chr11:64108241-64108291	PFSK-1	brain:	n/a
11	chr11:64108241-64108291	NB4	blood:	n/a
12	chr11:64108241-64108291	GM12891	blood:	n/a
13	chr11:64108241-64108291	PrEC	prostate:	n/a
14	chr11:64108241-64108291	A549	lung:	n/a
15	chr11:64108241-64108291	AG10803	skin:	n/a
16	chr11:64108241-64108291	Jurkat	blood:	n/a
17	chr11:64108241-64108291	HEK293	kidney:	embryo
18	chr11:64108241-64108291	BE2_C	brain:	n/a
19	chr11:64108241-64108291	SAEC	small airway:	n/a
20	chr11:64108241-64108291	PANC-1	pancreas:	n/a
21	chr11:64108241-64108291	NHDF-neo	bronchial:	n/a
22	chr11:64108241-64108291	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:64108241-64108291	GM12878	blood:	n/a
24	chr11:64108241-64108291	HIPEpiC	eye:	n/a
25	chr11:64108241-64108291	SK-N-SH	brain:	n/a
26	chr11:64108241-64108291	SK-N-SH_RA	brain:	n/a
27	chr11:64108241-64108291	HAEpiC	amniotic membrane:	n/a
28	chr11:64108241-64108291	HCT-116	colon:	n/a
29	chr11:64108241-64108291	HNPCEpiC	eye:	n/a
30	chr11:64108241-64108291	GM06990	blood:	n/a
31	chr11:64108241-64108291	AG09319	gingival:	n/a
32	chr11:64108241-64108291	T-47D	breast:	n/a
33	chr11:64108241-64108291	HMEC	breast:	n/a
34	chr11:64108241-64108291	HRE	kidney:	n/a
35	chr11:64108241-64108291	HRPEpiC	eye:	n/a
36	chr11:64108241-64108291	Hepatocyte	liver:	n/a
37	chr11:64108241-64108291	MCF-7	breast:	n/a
38	chr11:64108241-64108291	CMK	blood:	n/a
39	chr11:64108241-64108291	HUVEC	blood vessel:	n/a
40	chr11:64108241-64108291	HCF	heart:	n/a
41	chr11:64108241-64108291	MCF10A-Er-Src	breast:	n/a
42	chr11:64108241-64108291	AoSMC	blood vessel:	n/a
43	chr11:64108241-64108291	AG04450	lung:	fetal
44	chr11:64108241-64108291	U87	brain:	n/a
45	chr11:64108241-64108291	NT2-D1	testis:	n/a
46	chr11:64108241-64108291	ovcar-3	ovarian:	n/a
47	chr11:64108241-64108291	AG04449	skin:	fetal
48	chr11:64108241-64108291	Caco-2	colon:	n/a
49	chr11:64108241-64108291	GM19239	blood:	n/a
50	chr11:64108241-64108291	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64006889..64009385-chr11:64105672..64108941,3	K562	blood:
2	chr11:64108003..64110489-chr11:64126101..64127976,2	MCF-7	breast:
3	chr11:64078839..64083408-chr11:64108257..64111409,4	MCF-7	breast:
4	chr11:63951267..63954594-chr11:64105049..64110612,5	MCF-7	breast:
5	chr11:63972230..63976425-chr11:64106710..64112651,7	K562	blood:
6	chr11:64068655..64075946-chr11:64105786..64111623,11	K562	blood:
7	chr11:64085064..64087232-chr11:64106469..64111767,5	MCF-7	breast:

Variant related genes	Relation type
CCDC88B	TF binding region
CCDC88B	CpG island
ENSG00000173486	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000126432	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1047206	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11600990	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11606014	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12785488	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12788266	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12793347	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12798408	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12808002	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2276014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2286614	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2289573	0.81[AMR][1000 genomes]
rs28395875	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28395876	0.83[ASN][1000 genomes]
rs34292685	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34906890	0.83[AMR][1000 genomes]
rs35692796	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41294396	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs477895	0.88[EUR][1000 genomes]
rs66968227	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71456304	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71456310	0.81[AMR][1000 genomes]
rs7938380	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7939107	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7947143	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	231 gene(s)	inside rSNPs	diseases
6	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
7	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
8	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
10	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
11	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
12	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
13	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
14	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
15	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
16	nsv897685	chr11:64048912-64150370	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
17	nsv555192	chr11:64097233-64111928	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	n/a
18	nsv818840	chr11:64097233-64125142	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
19	nsv818841	chr11:64097233-64129722	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
20	nsv555193	chr11:64107143-64120574	Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	22 gene(s)	inside rSNPs	diseases
21	nsv897688	chr11:64107735-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs71456309	TEX40	cis	Esophagus Mucosa	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64099800-64108400	Weak transcription	Left Ventricle	heart
2	chr11:64099800-64109600	Weak transcription	Liver	Liver
3	chr11:64100000-64109000	Weak transcription	Pancreas	Pancrea
4	chr11:64103000-64108600	Weak transcription	A549	lung
5	chr11:64103000-64109600	Weak transcription	Right Atrium	heart
6	chr11:64103400-64109600	Weak transcription	NH-A	brain
7	chr11:64103800-64109400	Weak transcription	NHEK	skin
8	chr11:64104000-64108800	Weak transcription	HMEC	breast
9	chr11:64104200-64108600	Weak transcription	Stomach Mucosa	stomach
10	chr11:64106600-64108800	Flanking Active TSS	Primary B cells from cord blood	blood
11	chr11:64106800-64108600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
12	chr11:64106800-64108800	Flanking Active TSS	Fetal Thymus	thymus
13	chr11:64106800-64109000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr11:64106800-64110400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr11:64107000-64108400	Enhancers	Dnd41	blood
16	chr11:64107000-64108600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
17	chr11:64107000-64108800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr11:64107000-64109000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:64107200-64108400	Weak transcription	Gastric	stomach
20	chr11:64107200-64108800	Enhancers	Spleen	Spleen
21	chr11:64107200-64109400	Active TSS	Rectal Smooth Muscle	rectum
22	chr11:64107200-64110000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr11:64107400-64108400	Active TSS	Adipose Nuclei	Adipose
24	chr11:64107400-64108400	Active TSS	Duodenum Mucosa	Duodenum
25	chr11:64107400-64108600	Weak transcription	Hela-S3	cervix
26	chr11:64107400-64108800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
27	chr11:64107400-64109200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr11:64107600-64108400	Active TSS	Primary neutrophils fromperipheralblood	blood
29	chr11:64107600-64108400	Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr11:64107600-64108400	Active TSS	Primary T killer memory cells from peripheral blood	blood
31	chr11:64107600-64108400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:64107600-64108400	Active TSS	GM12878-XiMat	blood
33	chr11:64107800-64108400	Bivalent Enhancer	Fetal Stomach	stomach
34	chr11:64107800-64108600	Flanking Active TSS	Primary hematopoietic stem cells	blood
35	chr11:64107800-64108600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr11:64107800-64108600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
37	chr11:64107800-64108600	Active TSS	Brain Substantia Nigra	brain
38	chr11:64107800-64108800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:64107800-64108800	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr11:64107800-64108800	Enhancers	Stomach Smooth Muscle	stomach
41	chr11:64108000-64108400	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr11:64108000-64108400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:64108000-64108600	Active TSS	H1 Cell Line	embryonic stem cell
44	chr11:64108000-64108600	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr11:64108000-64108600	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr11:64108000-64108600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:64108000-64108600	Flanking Active TSS	Primary B cells from peripheral blood	blood
48	chr11:64108000-64108600	Active TSS	Brain Anterior Caudate	brain
49	chr11:64108000-64108800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr11:64108000-64109000	Active TSS	iPS-20b Cell Line	embryonic stem cell

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