Variant report

Variant	rs479777
Chromosome Location	chr11:64107477-64107478
allele	C/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	TBP	chr11:64107419-64107723	GM12878	blood:	n/a	n/a
2	GABPA	chr11:64107466-64107794	GM12878	blood:	n/a	n/a
3	POLR2A	chr11:64107291-64108469	GM12878	blood:	n/a	n/a
4	POLR2A	chr11:64107343-64108445	GM12892	blood:	n/a	n/a
5	RELA	chr11:64106984-64107965	GM19099	blood:	n/a	n/a
6	NFIC	chr11:64107000-64107903	GM12878	blood:	n/a	n/a
7	RELA	chr11:64107000-64107978	GM12891	blood:	n/a	n/a
8	POLR2A	chr11:64107266-64108404	GM12891	blood:	n/a	n/a
9	PML	chr11:64107081-64108570	GM12878	blood:	n/a	n/a
10	ZEB1	chr11:64107410-64107966	GM12878	blood:	n/a	n/a
11	POLR2A	chr11:64107178-64108434	GM12892	blood:	n/a	n/a
12	SPI1	chr11:64107393-64107939	GM12891	blood:	n/a	chr11:64107684-64107691 chr11:64107675-64107688 chr11:64107678-64107685 chr11:64107677-64107686 chr11:64107676-64107689 chr11:64107824-64107837
13	SPI1	chr11:64107354-64107896	GM12878	blood:	n/a	chr11:64107684-64107691 chr11:64107675-64107688 chr11:64107678-64107685 chr11:64107677-64107686 chr11:64107676-64107689 chr11:64107824-64107837
14	SPI1	chr11:64107400-64107937	HL-60	blood:	n/a	chr11:64107684-64107691 chr11:64107675-64107688 chr11:64107678-64107685 chr11:64107677-64107686 chr11:64107676-64107689 chr11:64107824-64107837
15	MAZ	chr11:64107154-64108557	GM12878	blood:	n/a	chr11:64107865-64107875 chr11:64108303-64108313
16	MXI1	chr11:64107350-64107813	GM12878	blood:	n/a	n/a
17	RELA	chr11:64107058-64108225	GM18951	blood:	n/a	n/a
18	PAX5	chr11:64107309-64108194	GM12878	blood:	n/a	chr11:64107676-64107685 chr11:64107682-64107691 chr11:64108006-64108025
19	POLR2A	chr11:64107414-64108812	HL-60	blood:	n/a	n/a
20	POLR2A	chr11:64106838-64108401	GM19099	blood:	n/a	n/a
21	PAX5	chr11:64107402-64107904	GM12892	blood:	n/a	chr11:64107676-64107685 chr11:64107682-64107691
22	POLR2A	chr11:64107316-64108393	GM12878	blood:	n/a	n/a
23	ELK1	chr11:64107304-64107871	GM12878	blood:	n/a	n/a
24	POLR2A	chr11:64106936-64108469	GM12878	blood:	n/a	n/a
25	TBL1XR1	chr11:64107116-64107894	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:64107062-64108493	GM12878	blood:	n/a	n/a
27	RUNX3	chr11:64107065-64108007	GM12878	blood:	n/a	n/a
28	SIN3A	chr11:64107403-64107861	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:64107316-64107740	GM12891	blood:	n/a	n/a
30	NFATC1	chr11:64107288-64107897	GM12878	blood:	n/a	n/a
31	POLR2A	chr11:64106788-64108606	GM12892	blood:	n/a	n/a
32	POLR2A	chr11:64107047-64108499	Raji	blood:	n/a	n/a
33	GABPA	chr11:64107418-64107855	GM12878	blood:	n/a	n/a
34	POLR2A	chr11:64107349-64108777	HL-60	blood:	n/a	n/a
35	TCF12	chr11:64107448-64107940	GM12878	blood:	n/a	chr11:64107804-64107814
36	POLR2A	chr11:64107329-64107862	GM12891	blood:	n/a	n/a
37	TCF3	chr11:64107380-64107905	GM12878	blood:	n/a	chr11:64107806-64107816 chr11:64107804-64107818 chr11:64107801-64107814
38	POLR2A	chr11:64107350-64108413	GM18526	blood:	n/a	n/a
39	GABPA	chr11:64107353-64108076	HL-60	blood:	n/a	n/a
40	CHD1	chr11:64107310-64108304	GM12878	blood:	n/a	n/a
41	EP300	chr11:64107420-64107827	GM12878	blood:	n/a	chr11:64107677-64107686
42	ELF1	chr11:64107144-64108941	GM12878	blood:	n/a	chr11:64107675-64107688 chr11:64107677-64107688 chr11:64107862-64107874
43	ELF1	chr11:64107389-64107980	GM12878	blood:	n/a	chr11:64107675-64107688 chr11:64107677-64107688 chr11:64107862-64107874
44	TCF12	chr11:64107439-64107910	GM12878	blood:	n/a	chr11:64107804-64107814
45	RUNX3	chr11:64107053-64108551	GM12878	blood:	n/a	n/a
46	POLR2A	chr11:64106985-64108487	GM12891	blood:	n/a	n/a
47	POU2F2	chr11:64107356-64107845	GM12891	blood:	n/a	n/a
48	ELF1	chr11:64107469-64107807	K562	blood:	n/a	chr11:64107675-64107688 chr11:64107677-64107688
49	EBF1	chr11:64107173-64107942	GM12878	blood:	n/a	n/a
50	BCLAF1	chr11:64107349-64107937	GM12878	blood:	n/a	chr11:64107813-64107826 chr11:64107500-64107508

No.	Distal block	Cell Line	Cell type
1	chr11:64006889..64009385-chr11:64105672..64108941,3	K562	blood:
2	chr11:63951267..63954594-chr11:64105049..64110612,5	MCF-7	breast:
3	chr11:64094386..64097437-chr11:64105553..64107544,3	K562	blood:
4	chr11:63972230..63976425-chr11:64106710..64112651,7	K562	blood:
5	chr11:64068655..64075946-chr11:64105786..64111623,11	K562	blood:
6	chr11:64085064..64087232-chr11:64106469..64111767,5	MCF-7	breast:
7	chr11:64106209..64107766-chr11:64119904..64122675,2	MCF-7	breast:

Variant related genes	Relation type
CCDC88B	TF binding region
ENSG00000168439	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000236935	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000149781	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 20 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10897488	0.83[MEX][hapmap]
rs11231757	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11601860	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1199046	0.86[JPT][hapmap];0.81[AMR][1000 genomes]
rs1783521	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2510066	0.92[CEU][hapmap];0.81[CHB][hapmap];0.87[CHD][hapmap];0.93[GIH][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs474901	0.83[MEX][hapmap]
rs479552	0.82[AMR][1000 genomes]
rs499425	0.92[CEU][hapmap];0.81[CHB][hapmap];0.93[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.86[TSI][hapmap];0.85[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs508168	0.83[MEX][hapmap]
rs510372	0.91[CHB][hapmap];0.84[CHD][hapmap];0.93[JPT][hapmap];0.87[MEX][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs516124	0.87[MEX][hapmap]
rs519763	0.86[JPT][hapmap];0.83[MEX][hapmap]
rs538147	0.87[MEX][hapmap]
rs566128	0.81[AMR][1000 genomes]
rs574087	0.88[CEU][hapmap];0.81[CHB][hapmap];0.93[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.86[TSI][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs574835	0.89[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs600377	0.85[JPT][hapmap]
rs612448	0.86[JPT][hapmap]
rs61886886	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs627425	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs645078	0.83[MEX][hapmap]
rs646153	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs647152	0.87[MEX][hapmap];0.82[AMR][1000 genomes]
rs663743	0.96[CEU][hapmap];0.81[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs694739	0.84[CEU][hapmap];0.81[CHB][hapmap];0.93[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];0.82[TSI][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs887314	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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

Variant related diseases (count:1)

Disease	PMID	Source
Sarcoidosis	22837380	GWAS catalog

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs479777	PPP1CA	cis	parietal	SCAN
rs479777	CCDC88B	cis	cerebellum	SCAN
rs479777	CCDC88B	cis	lymphoblastoid	seeQTL
rs479777	MALAT1	cis	cerebellum	SCAN
rs479777	CCDC88B	cis	multi-tissue	Pritchard
rs479777	C11orf68	cis	parietal	SCAN
rs479777	CYBASC3	cis	cerebellum	SCAN
rs479777	CCDC88B	cis	Esophagus Mucosa	GTEx
rs479777	SCGB2A2	cis	cerebellum	SCAN
rs479777	AP003774.1	cis	Whole Blood	GTEx
rs479777	TAF6L	cis	parietal	SCAN
rs479777	CCS	cis	cerebellum	SCAN
rs479777	CCDC88B	Cis_1M	lymphoblastoid	RTeQTL
rs479777	FKBP2	cis	cerebellum	SCAN
rs479777	FKBP2	cis	parietal	SCAN
rs479777	CTSW	cis	cerebellum	SCAN
rs479777	CHKA	cis	parietal	SCAN
rs479777	FLJ37970	cis	multi-tissue	Pritchard
rs479777	C11orf68	cis	cerebellum	SCAN

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64087000-64108200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:64099600-64107600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:64099800-64107600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr11:64099800-64108000	Weak transcription	Brain Anterior Caudate	brain
5	chr11:64099800-64108000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr11:64099800-64108200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr11:64099800-64108400	Weak transcription	Left Ventricle	heart
8	chr11:64099800-64109600	Weak transcription	Liver	Liver
9	chr11:64100000-64109000	Weak transcription	Pancreas	Pancrea
10	chr11:64100200-64108000	Weak transcription	Lung	lung
11	chr11:64100200-64108200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr11:64103000-64107800	Weak transcription	Right Ventricle	heart
13	chr11:64103000-64108600	Weak transcription	A549	lung
14	chr11:64103000-64109600	Weak transcription	Right Atrium	heart
15	chr11:64103400-64109600	Weak transcription	NH-A	brain
16	chr11:64103800-64109400	Weak transcription	NHEK	skin
17	chr11:64104000-64108800	Weak transcription	HMEC	breast
18	chr11:64104200-64108600	Weak transcription	Stomach Mucosa	stomach
19	chr11:64106400-64107600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr11:64106400-64107600	Flanking Active TSS	GM12878-XiMat	blood
21	chr11:64106400-64107800	Enhancers	Primary hematopoietic stem cells	blood
22	chr11:64106600-64108000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr11:64106600-64108800	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr11:64106800-64107600	Flanking Active TSS	Primary T cells from cord blood	blood
25	chr11:64106800-64107600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:64106800-64107800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:64106800-64108200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
28	chr11:64106800-64108600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
29	chr11:64106800-64108800	Flanking Active TSS	Fetal Thymus	thymus
30	chr11:64106800-64109000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr11:64106800-64110400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr11:64107000-64107600	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr11:64107000-64107600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:64107000-64107600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr11:64107000-64107600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:64107000-64107600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
37	chr11:64107000-64107600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr11:64107000-64107800	Enhancers	Brain Hippocampus Middle	brain
39	chr11:64107000-64107800	Enhancers	Esophagus	oesophagus
40	chr11:64107000-64107800	Flanking Active TSS	Thymus	Thymus
41	chr11:64107000-64108200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr11:64107000-64108200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
43	chr11:64107000-64108400	Enhancers	Dnd41	blood
44	chr11:64107000-64108600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:64107000-64108800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr11:64107000-64109000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:64107200-64107600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr11:64107200-64107600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
49	chr11:64107200-64107800	Flanking Active TSS	Colonic Mucosa	Colon
50	chr11:64107200-64107800	Weak transcription	Sigmoid Colon	Sigmoid Colon

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