Variant report

Variant	rs2839005
Chromosome Location	chr21:47240362-47240363
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47239959..47242449-chr21:47264107..47266678,2	K562	blood:
2	chr21:46712083..46713107-chr21:47240205..47240763,3	K562	blood:
3	chr21:47240324..47241096-chr21:47342788..47343697,3	MCF-7	breast:
4	chr21:47240141..47240932-chr21:47300508..47301042,2	MCF-7	breast:
5	chr21:46974512..46975479-chr21:47240182..47241018,3	MCF-7	breast:
6	chr21:47237629..47240751-chr21:47286627..47289424,3	MCF-7	breast:
7	chr21:46961701..46963309-chr21:47239137..47240693,2	K562	blood:
8	chr21:47160450..47161017-chr21:47239857..47240766,2	MCF-7	breast:
9	chr21:46973106..46978237-chr21:47237804..47242212,8	MCF-7	breast:
10	chr21:46961245..46963279-chr21:47238506..47240896,2	MCF-7	breast:
11	chr21:47062419..47066562-chr21:47239039..47241901,3	MCF-7	breast:
12	chr21:46369368..46370314-chr21:47240169..47241031,2	K562	blood:
13	chr21:46871841..46874571-chr21:47238507..47240724,2	MCF-7	breast:
14	chr21:46975702..46976554-chr21:47240286..47241105,4	MCF-7	breast:
15	chr21:46973481..46977035-chr21:47238682..47244036,11	MCF-7	breast:
16	chr21:47240289..47241171-chr21:47342639..47343656,4	MCF-7	breast:
17	chr21:47059881..47063838-chr21:47238507..47241456,3	MCF-7	breast:
18	chr21:46897608..46898629-chr21:47240205..47241125,3	K562	blood:
19	chr21:46974481..46976891-chr21:47239576..47241145,21	MCF-7	breast:
20	chr21:46975863..46976683-chr21:47240184..47241118,3	K562	blood:
21	chr21:46974938..46975481-chr21:47240107..47241154,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000183570	Chromatin interaction
ENSG00000173638	Chromatin interaction

Extended variants
information (count: 144 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:133)

rs_ID	r²[population]
rs1014446	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10854472	0.87[ASN][1000 genomes]
rs11089024	0.91[CHB][hapmap];0.84[JPT][hapmap];0.87[ASN][1000 genomes]
rs12329841	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12329855	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12481867	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12481913	0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12481970	0.86[ASN][1000 genomes]
rs12481977	0.87[ASN][1000 genomes]
rs12482010	0.86[ASN][1000 genomes]
rs12482094	0.83[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12482377	0.82[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12482405	0.86[EUR][1000 genomes]
rs12482648	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12482750	0.83[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs12482853	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1467758	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17351419	0.87[ASN][1000 genomes]
rs17351433	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2065334	0.80[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2094888	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2183595	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2183596	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2838973	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2838974	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2838976	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2838982	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2838989	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs2838990	0.82[ASN][1000 genomes]
rs2838991	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2838992	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2838993	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2838994	0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs2838995	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2838996	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2838997	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2838998	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2838999	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2839000	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2839001	0.95[ASN][1000 genomes]
rs2839002	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2839003	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2839004	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2839009	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2839013	0.85[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2839014	0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2839026	0.83[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2839029	0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2839032	0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs28583990	0.85[EUR][1000 genomes]
rs3367	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35781238	0.91[ASN][1000 genomes]
rs3788208	0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs3788209	0.87[ASN][1000 genomes]
rs3788211	0.81[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs3788215	0.85[ASN][1000 genomes]
rs3788216	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs3788220	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs3788224	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs3788227	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs3920695	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4434082	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4818798	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4818801	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4818802	0.87[ASN][1000 genomes]
rs4818803	0.87[ASN][1000 genomes]
rs4818805	0.83[ASN][1000 genomes]
rs4819151	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4819152	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4819154	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4819155	0.87[ASN][1000 genomes]
rs4819156	0.83[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs4819157	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs55707606	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55780126	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55856400	0.87[ASN][1000 genomes]
rs55875620	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55912352	0.87[ASN][1000 genomes]
rs55927540	0.90[ASN][1000 genomes]
rs56012600	0.84[EUR][1000 genomes]
rs56036552	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56256701	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56323347	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56347571	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56378934	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57688476	0.82[ASN][1000 genomes]
rs58952758	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59398815	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59785950	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60604183	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61063225	0.85[ASN][1000 genomes]
rs61100346	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61276251	0.82[ASN][1000 genomes]
rs62211883	0.87[ASN][1000 genomes]
rs62211885	0.87[ASN][1000 genomes]
rs62211886	0.87[ASN][1000 genomes]
rs62211895	0.87[ASN][1000 genomes]
rs62211925	0.87[ASN][1000 genomes]
rs62211926	0.87[ASN][1000 genomes]
rs62213555	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62214592	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62214596	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62214597	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62214599	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62214604	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62214608	0.83[ASN][1000 genomes]
rs66523344	0.87[ASN][1000 genomes]
rs66552772	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs66991496	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67055992	0.87[ASN][1000 genomes]
rs67878041	0.87[ASN][1000 genomes]
rs72497640	0.82[AMR][1000 genomes]
rs7276632	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7280173	0.87[ASN][1000 genomes]
rs8127369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8127428	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs8127809	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8128722	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs882668	0.81[ASN][1000 genomes]
rs882669	0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs914241	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9306139	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9637205	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9637206	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9637208	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9647230	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs964975	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9974491	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9977309	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9977908	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs9978078	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9978740	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs9983770	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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	nsv1058665	chr21:46719445-47634282	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
3	nsv544486	chr21:46719445-47634282	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
4	nsv1059230	chr21:46956877-47907990	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	n/a
5	nsv544491	chr21:46956877-47907990	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	n/a
6	nsv1058472	chr21:47027823-47797326	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	n/a
7	nsv544492	chr21:47027823-47797326	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	n/a
8	nsv428043	chr21:47179244-47471971	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	n/a
9	nsv1065959	chr21:47188878-48091343	Bivalent Enhancer Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	n/a
10	nsv914078	chr21:47218744-47311686	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
11	nsv531580	chr21:47221774-48090317	Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	n/a

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2839005	PCBP3	cis	Heart Left Ventricle	GTEx
rs2839005	PCBP3	cis	Muscle Skeletal	GTEx

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47217800-47260400	Weak transcription	Right Atrium	heart
2	chr21:47236400-47243800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr21:47237200-47241200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr21:47237200-47241400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr21:47237400-47240400	Weak transcription	Fetal Kidney	kidney
6	chr21:47237400-47240600	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr21:47237600-47240800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr21:47238000-47240400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr21:47238000-47240600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr21:47238000-47240600	Enhancers	HMEC	breast
11	chr21:47238200-47240600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr21:47238200-47240800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr21:47238200-47241000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr21:47238200-47241000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr21:47238200-47241000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr21:47238200-47241000	Enhancers	HSMM	muscle
17	chr21:47238400-47241000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr21:47238400-47241000	Enhancers	Muscle Satellite Cultured Cells	--
19	chr21:47238400-47241600	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr21:47238600-47240800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr21:47238600-47241000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr21:47238600-47241000	Enhancers	Fetal Muscle Leg	muscle
23	chr21:47238600-47241000	Enhancers	GM12878-XiMat	blood
24	chr21:47238800-47241000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr21:47238800-47241000	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr21:47238800-47241000	Enhancers	Brain Germinal Matrix	brain
27	chr21:47238800-47241800	Enhancers	Fetal Thymus	thymus
28	chr21:47239000-47240400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr21:47239000-47240400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr21:47239000-47240600	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr21:47239000-47241000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr21:47239000-47241000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr21:47239000-47241000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr21:47239000-47241000	Enhancers	NH-A	brain
35	chr21:47239000-47241200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr21:47239200-47241000	Enhancers	Fetal Brain Female	brain
37	chr21:47239200-47241000	Enhancers	Fetal Stomach	stomach
38	chr21:47239200-47241000	Enhancers	A549	lung
39	chr21:47239400-47240400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr21:47239400-47240400	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr21:47239400-47240600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr21:47239400-47240600	Enhancers	Fetal Intestine Large	intestine
43	chr21:47239400-47241000	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr21:47239400-47241000	Enhancers	Fetal Brain Male	brain
45	chr21:47239400-47247200	Weak transcription	Primary T cells from cord blood	blood
46	chr21:47239600-47240600	Genic enhancers	Thymus	Thymus
47	chr21:47239600-47240600	Enhancers	HSMMtube	muscle
48	chr21:47239600-47240800	Weak transcription	NHEK	skin
49	chr21:47239800-47240400	Enhancers	Spleen	Spleen
50	chr21:47239800-47240600	Weak transcription	NHLF	lung

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