Variant report

Variant	rs2297285
Chromosome Location	chr21:46705621-46705622
allele	A/G
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	chr21:46704196-46707066	IMR90	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:46493821..46495801-chr21:46704505..46706122,2	K562	blood:

Variant related genes	Relation type
ENSG00000215447	TF binding region
POFUT2	TF binding region
ENSG00000235374	Chromatin interaction
ENSG00000197381	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs1006779	0.87[CEU][hapmap]
rs10470258	0.82[CEU][hapmap]
rs1056099	0.86[CEU][hapmap]
rs11910831	0.84[EUR][1000 genomes]
rs1304487	0.82[CEU][hapmap]
rs13047598	0.84[CEU][hapmap]
rs13047688	0.83[EUR][1000 genomes]
rs13052356	1.00[CEU][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.83[EUR][1000 genomes]
rs13053002	0.89[EUR][1000 genomes]
rs1999333	0.87[CEU][hapmap]
rs1999334	0.87[CEU][hapmap]
rs2236445	0.87[CEU][hapmap]
rs2246697	0.87[CEU][hapmap]
rs2255774	0.87[CEU][hapmap]
rs2297284	1.00[CEU][hapmap];0.97[GIH][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2297286	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2330012	0.87[CEU][hapmap]
rs2330013	0.82[EUR][1000 genomes]
rs2838825	0.82[CEU][hapmap]
rs2838826	0.87[CEU][hapmap]
rs2838827	0.82[CEU][hapmap]
rs2838828	0.83[CEU][hapmap]
rs2838829	0.87[CEU][hapmap]
rs2838830	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs2838831	0.87[CEU][hapmap]
rs2838832	0.87[CEU][hapmap]
rs2838833	0.87[CEU][hapmap]
rs2838834	0.87[CEU][hapmap]
rs2838839	0.87[CEU][hapmap]
rs2838840	0.87[CEU][hapmap]
rs2838842	0.87[CEU][hapmap]
rs2838845	0.87[CEU][hapmap]
rs2838847	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs2838854	0.87[CEU][hapmap]
rs2838855	0.87[CEU][hapmap]
rs2838857	0.87[CEU][hapmap]
rs2838858	0.87[CEU][hapmap]
rs2838864	0.87[CEU][hapmap]
rs2838865	0.87[CEU][hapmap]
rs2838866	0.87[CEU][hapmap]
rs2838867	0.87[CEU][hapmap]
rs28628220	0.83[EUR][1000 genomes]
rs2877018	0.87[CEU][hapmap]
rs34886433	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3673	0.87[CEU][hapmap]
rs3746980	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs410184	0.82[ASW][hapmap]
rs4818769	0.84[EUR][1000 genomes]
rs4819035	0.82[ASW][hapmap];0.82[CEU][hapmap];0.85[MKK][hapmap]
rs4819039	0.82[CEU][hapmap]
rs4819041	0.87[CEU][hapmap]
rs4819049	0.86[CEU][hapmap]
rs4819051	0.87[CEU][hapmap]
rs4819052	0.94[EUR][1000 genomes]
rs7276828	0.87[CEU][hapmap]
rs733737	1.00[CEU][hapmap]
rs733738	1.00[CEU][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.84[EUR][1000 genomes]
rs733739	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs8126930	0.87[CEU][hapmap]
rs8130866	0.82[EUR][1000 genomes]
rs8131143	0.87[CEU][hapmap]
rs8134392	0.87[CEU][hapmap]
rs914217	0.86[EUR][1000 genomes]
rs914218	0.82[CEU][hapmap]
rs9306123	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9753963	0.86[CEU][hapmap]
rs9976074	0.87[CEU][hapmap]
rs9977178	0.87[CEU][hapmap]
rs9984901	1.00[CEU][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531546	chr21:46504151-47411772	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
2	nsv1059771	chr21:46561482-46830602	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv544481	chr21:46561482-46830602	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
4	nsv1063943	chr21:46571988-46819424	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv544482	chr21:46571988-46819424	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	nsv1064859	chr21:46571988-46830602	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
7	nsv544483	chr21:46571988-46830602	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
8	nsv1061691	chr21:46572641-46831862	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
9	nsv544484	chr21:46572641-46831862	Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
10	nsv587839	chr21:46580370-46837709	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
11	nsv587840	chr21:46580370-46839904	Bivalent Enhancer Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
12	nsv916959	chr21:46585681-46831845	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
13	nsv1063721	chr21:46610599-46907894	Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
14	nsv1059779	chr21:46611859-46891352	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
15	nsv544485	chr21:46611859-46891352	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
16	nsv1059805	chr21:46618210-46736943	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
17	nsv913999	chr21:46636844-46765251	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription 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 target site	43 gene(s)	inside rSNPs	diseases
18	nsv914000	chr21:46647078-46765251	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
19	nsv914001	chr21:46647078-46944113	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
20	nsv914002	chr21:46655638-46945024	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
21	nsv1057807	chr21:46656346-47077374	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
22	nsv914004	chr21:46670874-46736694	Enhancers Strong transcription Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
23	nsv914005	chr21:46670874-46756700	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
24	nsv914006	chr21:46670874-46788299	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
25	esv2762114	chr21:46680202-47067744	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
26	nsv914007	chr21:46684517-46780249	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
27	nsv914008	chr21:46684517-46792424	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
28	nsv914009	chr21:46684517-46908355	Enhancers Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
29	nsv1057661	chr21:46687476-46961041	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
30	nsv914010	chr21:46695039-46775018	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
31	nsv914011	chr21:46695039-46788299	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
32	nsv914012	chr21:46695039-47015661	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
33	nsv531547	chr21:46698078-46850908	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
34	nsv914013	chr21:46702506-46765251	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
35	nsv914014	chr21:46702506-46780249	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
36	nsv914015	chr21:46702506-46790203	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2297285	PCNT	cis	parietal	SCAN
rs2297285	CSTB	cis	parietal	SCAN
rs2297285	LOC642852	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46669200-46706600	Weak transcription	Right Atrium	heart
2	chr21:46676000-46706200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr21:46687800-46706600	Weak transcription	HMEC	breast
4	chr21:46689400-46706200	Strong transcription	HUES6 Cell Line	embryonic stem cell
5	chr21:46689600-46705800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
6	chr21:46689600-46706000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr21:46689600-46706000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr21:46689600-46706000	Strong transcription	Rectal Mucosa Donor 31	rectum
9	chr21:46689600-46706200	Strong transcription	Muscle Satellite Cultured Cells	--
10	chr21:46689600-46706200	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr21:46689600-46706200	Strong transcription	Placenta	Placenta
12	chr21:46689800-46706000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr21:46689800-46706200	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr21:46689800-46706200	Strong transcription	Osteobl	bone
15	chr21:46690000-46706000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr21:46690400-46706200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr21:46690600-46706200	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr21:46690800-46706000	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr21:46691000-46705800	Strong transcription	Brain Angular Gyrus	brain
20	chr21:46691000-46706200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr21:46691800-46705800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr21:46692000-46706000	Strong transcription	Fetal Intestine Large	intestine
23	chr21:46692000-46706200	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr21:46692200-46705800	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr21:46692200-46705800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr21:46692200-46706000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr21:46692200-46706000	Strong transcription	Liver	Liver
28	chr21:46692200-46706200	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr21:46692200-46706200	Strong transcription	Duodenum Mucosa	Duodenum
30	chr21:46692400-46706000	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr21:46692400-46706000	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr21:46692400-46706400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr21:46692600-46706200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr21:46693200-46706600	Strong transcription	Primary T cells from cord blood	blood
35	chr21:46693400-46705800	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr21:46693600-46706000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr21:46693600-46706000	Strong transcription	Left Ventricle	heart
38	chr21:46693600-46706000	Strong transcription	Right Ventricle	heart
39	chr21:46693800-46706200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr21:46694000-46706200	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr21:46694200-46705800	Strong transcription	NH-A	brain
42	chr21:46694200-46706000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr21:46694200-46706200	Strong transcription	H1 Cell Line	embryonic stem cell
44	chr21:46694200-46706200	Strong transcription	Adipose Nuclei	Adipose
45	chr21:46694400-46706000	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr21:46694400-46706000	Strong transcription	Placenta Amnion	Placenta Amnion
47	chr21:46694400-46706200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr21:46694400-46706200	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr21:46694400-46706200	Strong transcription	Brain Anterior Caudate	brain
50	chr21:46694400-46706200	Strong transcription	Brain Germinal Matrix	brain

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