Variant report

Variant	rs2070551
Chromosome Location	chr21:45616672-45616673
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	MAX	chr21:45616001-45616692	K562	blood:	n/a	chr21:45616217-45616226 chr21:45616213-45616222 chr21:45616215-45616225 chr21:45616214-45616224 chr21:45616259-45616268 chr21:45616213-45616228
2	POLR2A	chr21:45615804-45616806	GM12878	blood:	n/a	n/a
3	POLR2A	chr21:45615973-45616758	GM15510	blood:	n/a	n/a
4	PAX5	chr21:45615825-45616771	GM12878	blood:	n/a	chr21:45616279-45616288
5	CUX1	chr21:45616153-45616793	K562	blood:	n/a	n/a
6	POLR2A	chr21:45615997-45616709	GM19099	blood:	n/a	n/a
7	RUNX3	chr21:45615756-45616764	GM12878	blood:	n/a	n/a
8	POLR2A	chr21:45615955-45616687	GM18526	blood:	n/a	n/a
9	POLR2A	chr21:45615849-45616878	GM12892	blood:	n/a	n/a
10	GATA3	chr21:45615969-45616846	MCF-7	breast:	n/a	chr21:45616563-45616580
11	POU2F2	chr21:45616087-45616715	GM12891	blood:	n/a	n/a
12	JUN	chr21:45615817-45617579	K562	blood:	n/a	n/a
13	POLR2A	chr21:45615881-45616888	PBDE	blood:	n/a	n/a
14	MAZ	chr21:45616074-45616763	K562	blood:	n/a	chr21:45616217-45616226 chr21:45616213-45616222 chr21:45616215-45616225 chr21:45616214-45616224 chr21:45616259-45616268 chr21:45616213-45616228
15	PBX3	chr21:45616203-45616708	GM12878	blood:	n/a	n/a
16	CHD2	chr21:45615929-45616813	GM12878	blood:	n/a	chr21:45616323-45616333
17	ZMIZ1	chr21:45616152-45616693	K562	blood:	n/a	n/a
18	REST	chr21:45616050-45616717	PFSK-1	brain:	n/a	chr21:45616369-45616378 chr21:45616263-45616283 chr21:45616099-45616113 chr21:45616101-45616111
19	PML	chr21:45615478-45616718	GM12878	blood:	n/a	n/a
20	ATF2	chr21:45615953-45616749	GM12878	blood:	n/a	n/a
21	POLR2A	chr21:45616020-45616746	K562	blood:	n/a	n/a
22	POLR2A	chr21:45615795-45616933	GM12892	blood:	n/a	n/a
23	POLR2A	chr21:45615537-45617035	HL-60	blood:	n/a	n/a
24	POLR2A	chr21:45615971-45616727	GM12878	blood:	n/a	n/a
25	MAX	chr21:45616028-45616701	K562	blood:	n/a	chr21:45616217-45616226 chr21:45616213-45616222 chr21:45616215-45616225 chr21:45616214-45616224 chr21:45616259-45616268 chr21:45616213-45616228
26	TCF12	chr21:45616116-45616692	GM12878	blood:	n/a	chr21:45616594-45616604
27	HMGN3	chr21:45616081-45616737	K562	blood:	n/a	n/a
28	UBTF	chr21:45616210-45616702	K562	blood:	n/a	n/a
29	STAT5A	chr21:45615967-45616705	GM12878	blood:	n/a	n/a
30	EP300	chr21:45615851-45616768	GM12878	blood:	n/a	chr21:45616102-45616118 chr21:45616257-45616271
31	EP300	chr21:45615984-45616764	GM12878	blood:	n/a	chr21:45616102-45616118 chr21:45616257-45616271
32	RCOR1	chr21:45615890-45616801	K562	blood:	n/a	n/a
33	ELF1	chr21:45615878-45616918	GM12878	blood:	n/a	chr21:45616347-45616360 chr21:45616349-45616360
34	POLR2A	chr21:45615829-45616765	GM12892	blood:	n/a	n/a
35	MAX	chr21:45615881-45616691	GM12878	blood:	n/a	chr21:45616217-45616226 chr21:45616213-45616222 chr21:45616215-45616225 chr21:45616214-45616224 chr21:45616259-45616268 chr21:45616213-45616228
36	MAFK	chr21:45616187-45616749	K562	blood:	n/a	chr21:45616254-45616271
37	TCF3	chr21:45615936-45616789	GM12878	blood:	n/a	chr21:45616493-45616502 chr21:45616594-45616608 chr21:45616591-45616604 chr21:45616490-45616505
38	ZEB1	chr21:45616018-45616928	GM12878	blood:	n/a	chr21:45616781-45616788
39	MTA3	chr21:45615575-45616986	GM12878	blood:	n/a	n/a
40	CREB1	chr21:45615906-45616741	GM12878	blood:	n/a	n/a
41	RELA	chr21:45615939-45616819	GM15510	blood:	n/a	n/a
42	POLR2A	chr21:45616055-45616769	MCF-7	breast:	n/a	n/a
43	REST	chr21:45616032-45616805	MCF-7	breast:	n/a	chr21:45616369-45616378 chr21:45616263-45616283 chr21:45616099-45616113 chr21:45616101-45616111
44	MAZ	chr21:45616036-45616694	GM12878	blood:	n/a	chr21:45616217-45616226 chr21:45616213-45616222 chr21:45616215-45616225 chr21:45616214-45616224 chr21:45616259-45616268 chr21:45616213-45616228
45	SPI1	chr21:45615951-45616796	GM12878	blood:	n/a	chr21:45616349-45616358 chr21:45616348-45616361 chr21:45616350-45616357
46	BCLAF1	chr21:45615961-45616691	GM12878	blood:	n/a	chr21:45616371-45616379
47	POLR2A	chr21:45615946-45616875	GM12892	blood:	n/a	n/a
48	POLR2A	chr21:45615624-45617413	HL-60	blood:	n/a	n/a
49	MAX	chr21:45615733-45616951	MCF-7	breast:	n/a	chr21:45616217-45616226 chr21:45616213-45616222 chr21:45616215-45616225 chr21:45616214-45616224 chr21:45616259-45616268 chr21:45616213-45616228
50	TCF12	chr21:45615985-45616810	GM12878	blood:	n/a	chr21:45616594-45616604

No.	Distal block	Cell Line	Cell type
1	chr21:45565762..45568425-chr21:45616246..45618901,2	MCF-7	breast:
2	chr21:45593299..45595142-chr21:45615478..45617030,2	MCF-7	breast:
3	chr21:45557116..45559735-chr21:45615528..45618206,3	MCF-7	breast:
4	chr21:45616221..45617876-chr21:45625272..45628231,2	K562	blood:
5	chr21:45615502..45617869-chr21:45667459..45670293,2	K562	blood:
6	chr21:45615955..45617029-chr21:45660335..45661089,5	MCF-7	breast:
7	chr21:45610715..45617377-chr21:45717031..45721978,7	MCF-7	breast:
8	chr21:45568616..45570755-chr21:45615083..45617675,2	K562	blood:
9	chr21:45609075..45610927-chr21:45615037..45616803,2	K562	blood:
10	chr21:45615189..45618434-chr21:45625221..45628569,5	MCF-7	breast:
11	chr21:45614676..45619255-chr21:45657692..45665676,14	MCF-7	breast:
12	chr21:45595676..45596715-chr21:45615636..45617128,25	MCF-7	breast:
13	chr21:45595680..45596514-chr21:45615830..45617060,14	MCF-7	breast:
14	chr21:45612993..45620081-chr21:45620303..45625017,17	MCF-7	breast:
15	chr21:45567927..45569479-chr21:45614833..45617390,2	K562	blood:
16	chr21:45607137..45608941-chr21:45615370..45617109,2	K562	blood:
17	chr21:45570114..45570951-chr21:45616167..45617027,2	MCF-7	breast:
18	chr21:45595676..45596652-chr21:45615636..45617063,9	MCF-7	breast:
19	chr21:43796149..43796708-chr21:45616447..45617057,2	MCF-7	breast:
20	chr21:45615955..45617029-chr21:45660387..45661089,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000232124	TF binding region
ENSG00000232698	Chromatin interaction
ENSG00000267913	Chromatin interaction
ENSG00000232124	Chromatin interaction
ENSG00000160223	Chromatin interaction
ENSG00000141959	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11089118	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2070552	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2838516	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2838517	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2838519	0.92[CEU][hapmap];0.82[CHB][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2838520	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2838521	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2876932	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35405602	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3746958	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3804031	0.89[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3804032	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4317019	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4380337	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4456788	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4635612	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7276302	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7280525	1.00[YRI][hapmap]
rs7282490	0.96[CEU][hapmap];0.82[CHB][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs743478	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs743479	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs762421	0.96[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]
rs762422	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs762423	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8127691	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8130872	1.00[YRI][hapmap]
rs8134436	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33817	chr21:45169412-46031810	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv913887	chr21:45344799-45670770	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv1064420	chr21:45460089-45814986	Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
4	nsv544472	chr21:45460089-45814986	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
5	nsv432155	chr21:45479055-45772388	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
6	nsv913894	chr21:45508561-45627976	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	nsv913897	chr21:45528919-45640139	Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	esv1825445	chr21:45535566-45754936	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
9	esv1817474	chr21:45540607-45773102	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
10	nsv533679	chr21:45551026-45768578	Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription 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	64 gene(s)	inside rSNPs	diseases
11	nsv913898	chr21:45555079-45941566	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases
12	nsv428042	chr21:45560437-45848190	Enhancers Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer 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	61 gene(s)	inside rSNPs	diseases
13	nsv1065479	chr21:45571324-45617878	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv913900	chr21:45577102-45640139	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
15	esv3411301	chr21:45609579-45620771	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
16	esv3455479	chr21:45609616-45620726	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
17	esv3455480	chr21:45609633-45620722	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
18	nsv913901	chr21:45615741-45665330	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS 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	21 gene(s)	inside rSNPs	diseases
19	nsv913902	chr21:45615741-45709153	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45610800-45617600	Enhancers	Placenta	Placenta
2	chr21:45612200-45617200	Enhancers	Fetal Muscle Leg	muscle
3	chr21:45612800-45617400	Enhancers	Primary hematopoietic stem cells	blood
4	chr21:45613200-45617000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr21:45613600-45617200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr21:45613600-45617400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr21:45613600-45617400	Enhancers	Primary B cells from peripheral blood	blood
8	chr21:45614000-45617000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr21:45614000-45617200	Enhancers	GM12878-XiMat	blood
10	chr21:45614000-45617600	Enhancers	Primary B cells from cord blood	blood
11	chr21:45614400-45617400	Weak transcription	Brain Angular Gyrus	brain
12	chr21:45614800-45622400	Weak transcription	Pancreas	Pancrea
13	chr21:45615000-45617200	Weak transcription	Colonic Mucosa	Colon
14	chr21:45615000-45623200	Weak transcription	Brain Hippocampus Middle	brain
15	chr21:45615400-45616800	Weak transcription	Brain Anterior Caudate	brain
16	chr21:45615400-45622200	Weak transcription	Fetal Lung	lung
17	chr21:45615600-45616800	Enhancers	Primary T cells from cord blood	blood
18	chr21:45615600-45616800	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr21:45615600-45616800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr21:45615600-45617000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr21:45615600-45617000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr21:45615600-45617000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr21:45615600-45617000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr21:45615600-45617200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr21:45615600-45617200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr21:45615600-45617400	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr21:45615600-45617800	Enhancers	Fetal Thymus	thymus
28	chr21:45615800-45616800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr21:45615800-45616800	Enhancers	Spleen	Spleen
30	chr21:45615800-45617000	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr21:45615800-45617200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr21:45615800-45617400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr21:45615800-45617400	Enhancers	Brain Substantia Nigra	brain
34	chr21:45615800-45617600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr21:45615800-45617800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr21:45616000-45616800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr21:45616000-45616800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr21:45616000-45616800	Enhancers	Left Ventricle	heart
39	chr21:45616000-45616800	Bivalent Enhancer	Psoas Muscle	Psoas
40	chr21:45616000-45616800	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr21:45616000-45616800	Enhancers	Thymus	Thymus
42	chr21:45616000-45617200	Enhancers	Placenta Amnion	Placenta Amnion
43	chr21:45616000-45617600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr21:45616000-45618000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr21:45616000-45618000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr21:45616200-45616800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
47	chr21:45616200-45617200	Enhancers	Gastric	stomach
48	chr21:45616200-45617200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
49	chr21:45616200-45617600	Bivalent Enhancer	Adipose Nuclei	Adipose
50	chr21:45616400-45616800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin

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