Variant report

Variant	rs516124
Chromosome Location	chr11:64128423-64128424
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MTA3	chr11:64126109-64128842	GM12878	blood:	n/a	n/a
2	SPI1	chr11:64127948-64128508	HL-60	blood:	n/a	chr11:64128315-64128328
3	POLR2A	chr11:64125369-64128440	HL-60	blood:	n/a	n/a
4	YY1	chr11:64128238-64128499	GM12878	blood:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64082853..64088243-chr11:64119014..64129028,17	MCF-7	breast:
2	chr11:64008123..64009652-chr11:64126400..64128645,2	MCF-7	breast:
3	chr11:64125259..64126829-chr11:64127521..64129918,2	MCF-7	breast:
4	chr11:64125330..64128537-chr11:64215213..64218115,3	MCF-7	breast:
5	chr11:64070986..64076286-chr11:64124810..64128616,7	K562	blood:
6	chr11:64119430..64124364-chr11:64124831..64128743,7	MCF-7	breast:
7	chr11:64013219..64015249-chr11:64126039..64128658,2	K562	blood:
8	chr11:64069665..64072267-chr11:64127421..64129255,2	MCF-7	breast:

No data

Variant related genes	Relation type
RPS6KA4	TF binding region
ENSG00000173113	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000181908	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000173457	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000256940	Chromatin interaction
ENSG00000162302	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 15 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10792430	1.00[YRI][hapmap]
rs10897487	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10897488	1.00[ASW][hapmap];0.87[CEU][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11231757	0.84[AMR][1000 genomes]
rs11231770	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11231771	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11231772	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11542299	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11601651	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11601860	0.87[AMR][1000 genomes]
rs11606015	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11606081	1.00[ASW][hapmap];0.88[CEU][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1199045	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1199046	0.92[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1199047	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1662188	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1783521	0.84[AMR][1000 genomes]
rs17857342	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2510066	0.87[ASW][hapmap];0.87[MEX][hapmap]
rs3132740	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs474901	0.87[ASW][hapmap];0.81[CEU][hapmap];0.84[CHD][hapmap];0.95[GIH][hapmap];0.83[LWK][hapmap];0.95[MEX][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs475032	0.88[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs479552	0.81[AMR][1000 genomes]
rs479777	0.87[MEX][hapmap]
rs4930155	0.86[GIH][hapmap];0.87[MEX][hapmap]
rs499425	0.91[MEX][hapmap];0.83[AMR][1000 genomes]
rs508168	1.00[ASW][hapmap];0.88[CEU][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs510372	0.87[CEU][hapmap];0.98[GIH][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.85[TSI][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs519763	0.87[ASW][hapmap];0.81[CEU][hapmap];0.82[CHD][hapmap];0.98[GIH][hapmap];0.95[MEX][hapmap];0.87[MKK][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs521950	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs527465	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs538147	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs541207	0.89[GIH][hapmap];0.87[MEX][hapmap];0.80[TSI][hapmap]
rs542907	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs566128	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs574087	0.87[ASW][hapmap];0.91[MEX][hapmap];0.85[AMR][1000 genomes]
rs574835	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs600377	0.80[CEU][hapmap];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs612448	0.87[ASW][hapmap];0.81[CEU][hapmap];0.82[CHD][hapmap];0.98[GIH][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];0.82[TSI][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61886886	0.85[AMR][1000 genomes]
rs61886926	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs627425	0.82[AMR][1000 genomes]
rs645078	1.00[ASW][hapmap];0.88[CEU][hapmap];0.93[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs646153	0.83[AMR][1000 genomes]
rs647152	0.83[GIH][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap];0.81[AMR][1000 genomes]
rs663743	0.86[ASW][hapmap];0.82[MEX][hapmap]
rs694739	1.00[ASW][hapmap];0.87[MEX][hapmap]
rs72926005	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72926006	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs876064	0.88[YRI][hapmap]

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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	nsv897689	chr11:64109118-64148420	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
18	nsv897690	chr11:64118422-64135298	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
19	nsv897691	chr11:64118422-64137875	Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
20	nsv832187	chr11:64121969-64312300	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' 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	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:15)

SNP	Gene	Cis/trans	Tissue	Source
rs516124	PPP1CA	cis	parietal	SCAN
rs516124	FKBP2	cis	cerebellum	SCAN
rs516124	TAF6L	cis	parietal	SCAN
rs516124	C11orf68	cis	parietal	SCAN
rs516124	SCGB2A2	cis	cerebellum	SCAN
rs516124	C11orf68	cis	cerebellum	SCAN
rs516124	CCDC88B	cis	multi-tissue	Pritchard
rs516124	CCDC88B	cis	lymphoblastoid	seeQTL
rs516124	AP003774.1	cis	Whole Blood	GTEx
rs516124	CCDC88B	Cis_1M	lymphoblastoid	RTeQTL
rs516124	CCS	cis	cerebellum	SCAN
rs516124	FKBP2	cis	parietal	SCAN
rs516124	CCDC88B	cis	parietal	SCAN
rs516124	CHKA	cis	parietal	SCAN
rs516124	CCDC88B	cis	cerebellum	SCAN

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64125800-64128600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr11:64125800-64128600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr11:64127000-64129600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr11:64127400-64128600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr11:64127400-64128800	Weak transcription	Aorta	Aorta
6	chr11:64127400-64129600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:64127400-64129600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr11:64127400-64131600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr11:64127400-64136000	Weak transcription	Fetal Kidney	kidney
10	chr11:64127400-64140000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr11:64127400-64144400	Weak transcription	Psoas Muscle	Psoas
12	chr11:64127600-64128600	Weak transcription	NHDF-Ad	bronchial
13	chr11:64127600-64128800	Genic enhancers	Spleen	Spleen
14	chr11:64127600-64129000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr11:64127600-64129200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr11:64127600-64129400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:64127600-64129400	Weak transcription	HepG2	liver
18	chr11:64127600-64129600	Weak transcription	HUVEC	blood vessel
19	chr11:64127600-64129600	Weak transcription	K562	blood
20	chr11:64127600-64132800	Weak transcription	Small Intestine	intestine
21	chr11:64127600-64139600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr11:64127800-64128600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr11:64127800-64128600	Genic enhancers	Muscle Satellite Cultured Cells	--
24	chr11:64127800-64128600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr11:64127800-64128800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:64127800-64128800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr11:64127800-64128800	Genic enhancers	Primary T cells fromperipheralblood	blood
28	chr11:64127800-64128800	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr11:64127800-64128800	Genic enhancers	Placenta	Placenta
30	chr11:64127800-64128800	Transcr. at gene 5' and 3'	Hela-S3	cervix
31	chr11:64127800-64129000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr11:64127800-64129600	Weak transcription	HSMM	muscle
33	chr11:64127800-64130000	Genic enhancers	Fetal Thymus	thymus
34	chr11:64127800-64131600	Weak transcription	Right Atrium	heart
35	chr11:64127800-64132800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr11:64127800-64137600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:64127800-64139800	Strong transcription	Fetal Intestine Small	intestine
38	chr11:64127800-64146800	Weak transcription	Fetal Heart	heart
39	chr11:64128000-64128600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:64128000-64128600	Enhancers	Primary B cells from cord blood	blood
41	chr11:64128000-64128600	Genic enhancers	Primary B cells from peripheral blood	blood
42	chr11:64128000-64128600	Enhancers	Primary hematopoietic stem cells	blood
43	chr11:64128000-64128600	Genic enhancers	Fetal Muscle Leg	muscle
44	chr11:64128000-64128800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:64128000-64128800	Enhancers	Stomach Mucosa	stomach
46	chr11:64128000-64129000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
47	chr11:64128000-64129400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr11:64128000-64129400	Weak transcription	Osteobl	bone
49	chr11:64128000-64129600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:64128000-64129600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood

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