Variant report

Variant	rs12626759
Chromosome Location	chr21:46351134-46351135
allele	G/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	STAT3	chr21:46351110-46351511	MCF10A-Er-Src	breast:	n/a	chr21:46351430-46351444 chr21:46351447-46351455
2	POLR2A	chr21:46350950-46351554	HL-60	blood:	n/a	n/a
3	RELA	chr21:46349482-46351776	GM15510	blood:	n/a	n/a
4	YY1	chr21:46351054-46351259	GM12878	blood:	n/a	n/a
5	EBF1	chr21:46350249-46351549	GM12878	blood:	n/a	chr21:46351222-46351233 chr21:46351223-46351232 chr21:46351223-46351232 chr21:46351221-46351234
6	ELF1	chr21:46349709-46352433	GM12878	blood:	n/a	chr21:46351065-46351077 chr21:46351566-46351578
7	NFATC1	chr21:46350982-46351481	GM12878	blood:	n/a	chr21:46351263-46351277
8	POLR2A	chr21:46349243-46352888	GM18526	blood:	n/a	n/a
9	POLR2A	chr21:46350964-46351642	HL-60	blood:	n/a	n/a
10	RELA	chr21:46350645-46351544	GM19099	blood:	n/a	n/a
11	PAX5	chr21:46351075-46351548	GM12878	blood:	n/a	chr21:46351207-46351216
12	NFIC	chr21:46350574-46351538	GM12878	blood:	n/a	n/a
13	BCL11A	chr21:46351119-46351342	GM12878	blood:	n/a	n/a
14	MAX	chr21:46350644-46351487	NB4	blood:	n/a	chr21:46350706-46350715 chr21:46351194-46351204 chr21:46351169-46351179
15	POLR2A	chr21:46350220-46353474	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr21:46349081-46351931	GM12878	blood:	n/a	chr21:46351222-46351233 chr21:46351223-46351232 chr21:46351223-46351232 chr21:46351221-46351234
17	EGR1	chr21:46350987-46351295	K562	blood:	n/a	chr21:46351187-46351201 chr21:46351207-46351216 chr21:46351196-46351209
18	EBF1	chr21:46349672-46351552	GM12878	blood:	n/a	chr21:46351222-46351233 chr21:46351223-46351232 chr21:46351223-46351232 chr21:46351221-46351234
19	EP300	chr21:46350996-46351442	GM12878	blood:	n/a	n/a
20	POLR2A	chr21:46351051-46351939	GM12892	blood:	n/a	n/a
21	RELA	chr21:46350609-46351526	GM12891	blood:	n/a	n/a
22	ETS1	chr21:46351012-46351407	GM12878	blood:	n/a	chr21:46351208-46351215 chr21:46351189-46351200 chr21:46351202-46351216 chr21:46351110-46351124 chr21:46351111-46351122 chr21:46351204-46351215
23	SPI1	chr21:46351005-46351393	GM12891	blood:	n/a	chr21:46351209-46351216 chr21:46351206-46351219
24	POLR2A	chr21:46350875-46351900	SK-N-MC	brain:	n/a	n/a
25	SUZ12	chr21:46350785-46352900	NT2-D1	testis:	n/a	n/a
26	BHLHE40	chr21:46350678-46351617	GM12878	blood:	n/a	n/a
27	TBL1XR1	chr21:46351018-46351499	GM12878	blood:	n/a	n/a
28	POLR2A	chr21:46350960-46351151	K562	blood:	n/a	n/a
29	MAX	chr21:46350524-46352252	GM12878	blood:	n/a	chr21:46350706-46350715 chr21:46351194-46351204 chr21:46351169-46351179
30	POLR2A	chr21:46350524-46352839	MCF10A-Er-Src	breast:	n/a	n/a
31	IKZF1	chr21:46350899-46351446	GM12878	blood:	n/a	n/a
32	MTA3	chr21:46351033-46351564	GM12878	blood:	n/a	n/a
33	MTA3	chr21:46349056-46351679	GM12878	blood:	n/a	n/a
34	CEBPB	chr21:46350949-46351595	GM12878	blood:	n/a	n/a
35	ZNF143	chr21:46351063-46351930	GM12878	blood:	n/a	chr21:46351693-46351703 chr21:46351440-46351455 chr21:46351145-46351163 chr21:46351391-46351409
36	RUNX3	chr21:46350889-46351662	GM12878	blood:	n/a	n/a
37	CEBPB	chr21:46350960-46351158	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr21:46350754-46351942	GM12878	blood:	n/a	chr21:46351189-46351199
39	POLR2A	chr21:46351099-46351610	GM12878	blood:	n/a	n/a
40	TBP	chr21:46350706-46351461	GM12878	blood:	n/a	n/a
41	POLR2A	chr21:46350202-46352838	GM18505	blood:	n/a	n/a
42	POU2F2	chr21:46350991-46351514	GM12878	blood:	n/a	chr21:46351014-46351026
43	CUX1	chr21:46350729-46351885	GM12878	blood:	n/a	n/a
44	PML	chr21:46350758-46351594	GM12878	blood:	n/a	n/a
45	POLR2A	chr21:46351093-46351886	GM10847	blood:	n/a	n/a
46	POLR2A	chr21:46349053-46353060	GM18951	blood:	n/a	n/a
47	MXI1	chr21:46350613-46351526	GM12878	blood:	n/a	n/a
48	POLR2A	chr21:46349622-46353037	GM15510	blood:	n/a	n/a
49	ATF2	chr21:46351008-46351474	GM12878	blood:	n/a	n/a
50	POLR2A	chr21:46350927-46351523	SK-N-MC	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:46351118-46351168	RPTEC	kidney:	n/a
2	chr21:46351118-46351168	HCT-116	colon:	n/a
3	chr21:46351118-46351168	A549	lung:	n/a
4	chr21:46351118-46351168	Jurkat	blood:	n/a
5	chr21:46351118-46351168	K562	blood:	n/a
6	chr21:46351118-46351168	ProgFib	skin:	n/a
7	chr21:46351118-46351168	BE2_C	brain:	n/a
8	chr21:46351118-46351168	AoSMC	blood vessel:	n/a
9	chr21:46351118-46351168	HEEpiC	esophagus:	n/a
10	chr21:46351118-46351168	NH-A	brain:	n/a
11	chr21:46351118-46351168	GM06990	blood:	n/a
12	chr21:46351118-46351168	SKMC	muscle:	n/a
13	chr21:46351118-46351168	CMK	blood:	n/a
14	chr21:46351118-46351168	ovcar-3	ovarian:	n/a
15	chr21:46351118-46351168	AG10803	skin:	n/a
16	chr21:46351118-46351168	HPAEpiC	pulmonary alveolar:	n/a
17	chr21:46351118-46351168	PANC-1	pancreas:	n/a
18	chr21:46351118-46351168	GM12878	blood:	n/a
19	chr21:46351118-46351168	H1-hESC	embryonic stem cell:	embryo
20	chr21:46351118-46351168	AG04449	skin:	fetal
21	chr21:46351118-46351168	NHDF-neo	bronchial:	n/a
22	chr21:46351118-46351168	MCF10A-Er-Src	breast:	n/a
23	chr21:46351118-46351168	HNPCEpiC	eye:	n/a
24	chr21:46351118-46351168	BJ	skin:	n/a
25	chr21:46351118-46351168	ECC-1	luminal epithelium:	n/a
26	chr21:46351118-46351168	GM19239	blood:	n/a
27	chr21:46351118-46351168	PrEC	prostate:	n/a
28	chr21:46351118-46351168	HMEC	breast:	n/a
29	chr21:46351118-46351168	U87	brain:	n/a
30	chr21:46351118-46351168	GM12891	blood:	n/a
31	chr21:46351118-46351168	HRE	kidney:	n/a
32	chr21:46351118-46351168	HAEpiC	amniotic membrane:	n/a
33	chr21:46351118-46351168	SK-N-SH_RA	brain:	n/a
34	chr21:46351118-46351168	LNCaP	prostate:	n/a
35	chr21:46351118-46351168	Caco-2	colon:	n/a
36	chr21:46351118-46351168	HUVEC	blood vessel:	n/a
37	chr21:46351118-46351168	Hela-S3	cervix:	n/a
38	chr21:46351118-46351168	T-47D	breast:	n/a
39	chr21:46351118-46351168	HL-60	blood:	n/a
40	chr21:46351118-46351168	IMR90	lung:	fetal
41	chr21:46351118-46351168	HRPEpiC	eye:	n/a
42	chr21:46351118-46351168	HRCEpiC	kidney:	n/a
43	chr21:46351118-46351168	NB4	blood:	n/a
44	chr21:46351118-46351168	SK-N-MC	brain:	n/a
45	chr21:46351118-46351168	HepG2	liver:	n/a
46	chr21:46351118-46351168	SK-N-SH	brain:	n/a
47	chr21:46351118-46351168	PFSK-1	brain:	n/a
48	chr21:46351118-46351168	GM12892	blood:	n/a
49	chr21:46351118-46351168	AG09309	skin:	n/a
50	chr21:46351118-46351168	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr21:46348854..46378176-chr21:46489799..46500436,75	K562	blood:
2	chr21:46220228..46226309-chr21:46349546..46355767,8	K562	blood:
3	chr21:46345821..46352717-chr21:46492682..46495835,7	MCF-7	breast:
4	chr21:46348334..46352514-chr21:46492914..46497675,5	K562	blood:
5	chr21:46234565..46238085-chr21:46349825..46353215,3	MCF-7	breast:
6	chr21:46348891..46351856-chr21:46356275..46360285,3	K562	blood:
7	chr21:46288744..46296879-chr21:46346201..46354260,26	MCF-7	breast:
8	chr21:46220263..46223201-chr21:46349640..46352735,4	K562	blood:

Variant related genes	Relation type
ENSG00000273027	TF binding region
ITGB2	TF binding region
ITGB2	CpG island
ENSG00000273027	CpG island
ENSG00000197381	Chromatin interaction
ENSG00000236519	Chromatin interaction
ENSG00000183255	Chromatin interaction
ENSG00000183250	Chromatin interaction
ENSG00000184900	Chromatin interaction
ENSG00000160256	Chromatin interaction
ENSG00000235374	Chromatin interaction
ENSG00000268856	Chromatin interaction
ENSG00000184787	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1721	0.80[EUR][1000 genomes]
rs7276960	0.80[EUR][1000 genomes]
rs7281820	0.80[EUR][1000 genomes]
rs9974949	0.81[EUR][1000 genomes]
rs9975055	0.80[EUR][1000 genomes]
rs9983621	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 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	esv1808790	chr21:46349496-46355712	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
23	esv3428377	chr21:46350818-46351144	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46340600-46351400	Weak transcription	Right Atrium	heart
2	chr21:46345600-46351200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr21:46346000-46352000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
4	chr21:46346200-46352200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr21:46347000-46351800	Enhancers	Spleen	Spleen
6	chr21:46348200-46351200	Enhancers	Primary hematopoietic stem cells	blood
7	chr21:46348200-46351400	Bivalent Enhancer	Fetal Muscle Leg	muscle
8	chr21:46349000-46351800	Flanking Active TSS	GM12878-XiMat	blood
9	chr21:46349200-46351200	Weak transcription	A549	lung
10	chr21:46349400-46351600	Bivalent Enhancer	NHEK	skin
11	chr21:46349600-46351200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr21:46349600-46351200	Weak transcription	HSMMtube	muscle
13	chr21:46349800-46351200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
14	chr21:46349800-46351200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
15	chr21:46349800-46351200	Bivalent Enhancer	Placenta	Placenta
16	chr21:46349800-46351400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
17	chr21:46349800-46352400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
18	chr21:46350000-46351400	Enhancers	Liver	Liver
19	chr21:46350000-46351600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
20	chr21:46350000-46351800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr21:46350000-46352400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr21:46350200-46351400	Flanking Active TSS	Fetal Thymus	thymus
23	chr21:46350200-46351800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
24	chr21:46350200-46351800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr21:46350200-46351800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
26	chr21:46350200-46351800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr21:46350200-46351800	Flanking Active TSS	Dnd41	blood
28	chr21:46350200-46352000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr21:46350200-46352600	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr21:46350400-46351200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr21:46350400-46351200	Weak transcription	Pancreas	Pancrea
32	chr21:46350400-46351400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr21:46350400-46351400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr21:46350400-46351400	Enhancers	HepG2	liver
35	chr21:46350400-46352800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
36	chr21:46350600-46351200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr21:46350600-46351200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr21:46350600-46351200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr21:46350600-46351200	Bivalent Enhancer	Fetal Stomach	stomach
40	chr21:46350600-46351200	Bivalent Enhancer	NH-A	brain
41	chr21:46350600-46351400	Bivalent Enhancer	Adipose Nuclei	Adipose
42	chr21:46350600-46351600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr21:46350600-46351600	Flanking Active TSS	Osteobl	bone
44	chr21:46350600-46351800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr21:46350600-46351800	Flanking Active TSS	Primary B cells from peripheral blood	blood
46	chr21:46350600-46351800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr21:46350600-46352000	Flanking Active TSS	Thymus	Thymus
48	chr21:46350600-46353000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr21:46350600-46353200	Bivalent Enhancer	Fetal Lung	lung
50	chr21:46350800-46351200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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