Variant report

Variant	rs12482042
Chromosome Location	chr21:46359427-46359428
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	JUND	chr21:46359154-46360074	K562	blood:	n/a	n/a
2	MAX	chr21:46359047-46360590	K562	blood:	n/a	chr21:46360118-46360128
3	MAX	chr21:46359325-46360554	HepG2	liver:	n/a	chr21:46360118-46360128
4	POLR2A	chr21:46359340-46360607	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr21:46358524-46360361	GM18505	blood:	n/a	n/a
6	CHD1	chr21:46359328-46361037	IMR90	lung:	n/a	n/a
7	MBD4	chr21:46359292-46360058	HepG2	liver:	n/a	n/a
8	IRF1	chr21:46359349-46360094	K562	blood:	n/a	n/a
9	MXI1	chr21:46358871-46361050	SK-N-SH	brain:	n/a	n/a
10	CBX3	chr21:46359391-46360076	K562	blood:	n/a	n/a
11	POLR2A	chr21:46358166-46360480	SK-N-MC	brain:	n/a	n/a
12	JUN	chr21:46358206-46361110	K562	blood:	n/a	chr21:46358894-46358905
13	E2F4	chr21:46359357-46360250	K562	blood:	n/a	chr21:46360122-46360132 chr21:46359882-46359892
14	NR2F2	chr21:46359427-46360175	MCF-7	breast:	n/a	n/a
15	GABPA	chr21:46359399-46360137	SK-N-SH	brain:	n/a	chr21:46359828-46359842
16	YY1	chr21:46359383-46360086	H1-hESC	embryonic stem cell:	n/a	chr21:46359834-46359848 chr21:46359864-46359875 chr21:46359878-46359889 chr21:46359866-46359875
17	GABPA	chr21:46359338-46360563	MCF-7	breast:	n/a	chr21:46359828-46359842
18	TAF1	chr21:46359379-46360399	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr21:46359377-46359999	K562	blood:	n/a	n/a
20	MAX	chr21:46359188-46360520	K562	blood:	n/a	chr21:46360118-46360128
21	POLR2A	chr21:46358504-46360381	GM12878	blood:	n/a	n/a
22	ZNF263	chr21:46359023-46360700	HEK293-T-REx	kidney:	n/a	n/a
23	MTA3	chr21:46359371-46360072	GM12878	blood:	n/a	n/a
24	POLR2A	chr21:46359394-46360527	GM12892	blood:	n/a	n/a
25	MAX	chr21:46359318-46360394	H1-hESC	embryonic stem cell:	n/a	chr21:46360118-46360128
26	MYC	chr21:46359272-46360588	K562	blood:	n/a	chr21:46360118-46360128
27	SREBP2	chr21:46359170-46360256	GM12878	blood:	n/a	n/a
28	RCOR1	chr21:46359423-46359432	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr21:46359261-46360302	PFSK-1	brain:	n/a	n/a
30	E2F6	chr21:46359104-46360366	K562	blood:	n/a	chr21:46360122-46360132 chr21:46359882-46359892
31	ELF1	chr21:46359389-46360165	GM12878	blood:	n/a	chr21:46359846-46359857 chr21:46359861-46359873 chr21:46359847-46359856 chr21:46359846-46359855 chr21:46359846-46359857 chr21:46359845-46359858 chr21:46360115-46360127 chr21:46359928-46359937
32	MAX	chr21:46359279-46360463	HepG2	liver:	n/a	chr21:46360118-46360128
33	PML	chr21:46359363-46360217	GM12878	blood:	n/a	n/a
34	RCOR1	chr21:46359328-46360030	GM12878	blood:	n/a	n/a
35	POLR2A	chr21:46359405-46360185	GM12892	blood:	n/a	n/a
36	MYC	chr21:46359389-46360610	K562	blood:	n/a	chr21:46360118-46360128
37	E2F6	chr21:46359338-46360032	K562	blood:	n/a	chr21:46359882-46359892
38	YY1	chr21:46359398-46360070	GM12878	blood:	n/a	chr21:46359834-46359848 chr21:46359864-46359875 chr21:46359878-46359889 chr21:46359866-46359875
39	RCOR1	chr21:46359307-46360037	K562	blood:	n/a	n/a
40	MAX	chr21:46359385-46360440	K562	blood:	n/a	chr21:46360118-46360128
41	POLR2A	chr21:46358401-46360539	K562	blood:	n/a	n/a
42	MAX	chr21:46359184-46360501	HCT-116	colon:	n/a	chr21:46360118-46360128
43	MAX	chr21:46359344-46360254	HCT-116	colon:	n/a	chr21:46360118-46360128
44	YY1	chr21:46359382-46360064	ECC-1	luminal epithelium:	n/a	chr21:46359834-46359848 chr21:46359864-46359875 chr21:46359878-46359889 chr21:46359866-46359875
45	ELF1	chr21:46359165-46360440	GM12878	blood:	n/a	chr21:46359846-46359857 chr21:46359861-46359873 chr21:46359847-46359856 chr21:46360168-46360177 chr21:46359846-46359855 chr21:46359846-46359857 chr21:46359845-46359858 chr21:46360115-46360127 chr21:46359928-46359937
46	CTBP2	chr21:46359419-46359967	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr21:46358394-46360437	GM19099	blood:	n/a	n/a
48	POLR2A	chr21:46359001-46360543	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr21:46358340-46360742	GM12891	blood:	n/a	n/a
50	ETS1	chr21:46359243-46360410	K562	blood:	n/a	chr21:46359856-46359865 chr21:46359844-46359854 chr21:46359854-46359864 chr21:46359856-46359865 chr21:46359855-46359868 chr21:46359856-46359865 chr21:46359856-46359872 chr21:46359856-46359865 chr21:46359856-46359865

No.	Distal block	Cell Line	Cell type
1	chr21:46358120..46360078-chr21:46493208..46495098,2	MCF-7	breast:
2	chr21:46348854..46378176-chr21:46489799..46500436,75	K562	blood:
3	chr21:46235785..46239443-chr21:46357143..46362674,8	MCF-7	breast:
4	chr21:46291916..46297365-chr21:46358001..46363812,14	MCF-7	breast:
5	chr21:46358715..46360802-chr21:46377914..46380232,3	K562	blood:
6	chr21:46358799..46362946-chr21:46546409..46551680,5	K562	blood:
7	chr21:46353923..46356909-chr21:46357554..46361249,6	K562	blood:
8	chr21:46348891..46351856-chr21:46356275..46360285,3	K562	blood:
9	chr21:46236285..46239693-chr21:46357237..46360614,5	K562	blood:
10	chr21:46357049..46359694-chr21:46468700..46471270,2	K562	blood:
11	chr21:46355061..46362857-chr21:46490375..46496482,13	K562	blood:
12	chr21:46236918..46239386-chr21:46357793..46361272,3	K562	blood:
13	chr21:46357121..46360685-chr21:46377277..46380905,4	MCF-7	breast:
14	chr21:46218606..46224662-chr21:46357422..46363606,13	MCF-7	breast:
15	chr21:46220260..46222802-chr21:46358731..46365262,8	MCF-7	breast:

Variant related genes	Relation type
FAM207A	TF binding region
ENSG00000272825	Chromatin interaction
ENSG00000273027	Chromatin interaction
ENSG00000235374	Chromatin interaction
ENSG00000183255	Chromatin interaction
ENSG00000184787	Chromatin interaction
ENSG00000197381	Chromatin interaction
ENSG00000160256	Chromatin interaction
ENSG00000184900	Chromatin interaction
ENSG00000268856	Chromatin interaction
ENSG00000236519	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11909342	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11911785	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12482536	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12483718	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17313439	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2225435	0.86[ASN][1000 genomes]
rs2294167	0.86[ASN][1000 genomes]
rs28448476	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28515630	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs394531	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62214492	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62214499	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7282201	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8132726	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9978038	0.89[EUR][1000 genomes]
rs9979028	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9980281	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9981033	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv1056513	chr21:46254075-46442759	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv913969	chr21:46279505-46472929	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv913970	chr21:46305175-46487831	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv933240	chr21:46305956-46371518	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv913974	chr21:46306161-46430792	Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv913975	chr21:46306161-46459432	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv913976	chr21:46306161-46487831	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv834110	chr21:46316183-46505151	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
10	nsv1064518	chr21:46317690-46413159	Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv913977	chr21:46335761-46454391	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv913978	chr21:46335761-46466674	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	nsv913979	chr21:46335761-46472929	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
14	nsv913980	chr21:46337565-46454391	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
15	nsv913981	chr21:46344426-46408790	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
16	nsv913982	chr21:46344426-46430792	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
17	nsv913984	chr21:46344426-46435610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS 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	21 gene(s)	inside rSNPs	diseases
18	nsv913983	chr21:46344426-46440385	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
19	nsv913985	chr21:46344426-46448142	Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
20	nsv913986	chr21:46344426-46466674	Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
21	nsv913987	chr21:46344426-46472929	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
22	nsv913988	chr21:46356816-46408790	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
23	nsv913989	chr21:46356816-46430792	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer 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	18 gene(s)	inside rSNPs	diseases
24	nsv913990	chr21:46356816-46448142	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
25	nsv913991	chr21:46356816-46472929	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12482042	C21orf69	cis	multi-tissue	Pritchard

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46358600-46359600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
2	chr21:46358600-46359600	Flanking Active TSS	Dnd41	blood
3	chr21:46358600-46359600	Flanking Active TSS	HMEC	breast
4	chr21:46358600-46359600	Flanking Active TSS	NHEK	skin
5	chr21:46358800-46359600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
6	chr21:46358800-46359600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr21:46358800-46359600	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr21:46358800-46359600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr21:46358800-46359600	Enhancers	Spleen	Spleen
10	chr21:46358800-46360600	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr21:46358800-46360800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr21:46358800-46361000	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr21:46359000-46359600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr21:46359000-46359600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr21:46359000-46359600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
16	chr21:46359000-46359600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
17	chr21:46359000-46359600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr21:46359000-46359600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr21:46359000-46359600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
20	chr21:46359000-46359600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
21	chr21:46359000-46359600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr21:46359000-46359600	Flanking Active TSS	Liver	Liver
23	chr21:46359000-46359600	Flanking Active TSS	Brain Cingulate Gyrus	brain
24	chr21:46359000-46359600	Flanking Active TSS	Fetal Muscle Trunk	muscle
25	chr21:46359000-46359600	Flanking Active TSS	Fetal Muscle Leg	muscle
26	chr21:46359000-46359600	Flanking Active TSS	Pancreas	Pancrea
27	chr21:46359000-46359600	Flanking Active TSS	HUVEC	blood vessel
28	chr21:46359000-46359600	Flanking Active TSS	NH-A	brain
29	chr21:46359000-46359600	Flanking Active TSS	Osteobl	bone
30	chr21:46359000-46359800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr21:46359000-46359800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
32	chr21:46359000-46359800	Flanking Active TSS	Fetal Thymus	thymus
33	chr21:46359000-46359800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr21:46359000-46361000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr21:46359000-46361000	Active TSS	Fetal Kidney	kidney
36	chr21:46359000-46361200	Active TSS	A549	lung
37	chr21:46359000-46361600	Active TSS	H9 Cell Line	embryonic stem cell
38	chr21:46359000-46361600	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr21:46359200-46359600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr21:46359200-46359600	Flanking Active TSS	Primary B cells from peripheral blood	blood
41	chr21:46359200-46359600	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr21:46359200-46359600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr21:46359200-46359600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
44	chr21:46359200-46359600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr21:46359200-46359600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr21:46359200-46359600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr21:46359200-46359600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
48	chr21:46359200-46359600	Flanking Active TSS	Placenta	Placenta
49	chr21:46359200-46359600	Flanking Active TSS	Ovary	ovary
50	chr21:46359200-46359600	Flanking Active TSS	Right Ventricle	heart

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