Variant report

Variant	rs56199687
Chromosome Location	chr21:46360567-46360568
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	MAX	chr21:46359047-46360590	K562	blood:	n/a	chr21:46360118-46360128
2	POLR2A	chr21:46359340-46360607	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD1	chr21:46359328-46361037	IMR90	lung:	n/a	n/a
4	SIN3AK20	chr21:46359520-46360568	K562	blood:	n/a	n/a
5	MXI1	chr21:46358871-46361050	SK-N-SH	brain:	n/a	n/a
6	MYC	chr21:46359525-46360691	K562	blood:	n/a	chr21:46360118-46360128
7	JUN	chr21:46358206-46361110	K562	blood:	n/a	chr21:46358894-46358905
8	ZNF384	chr21:46360361-46360800	K562	blood:	n/a	n/a
9	HEY1	chr21:46359472-46360599	K562	blood:	n/a	chr21:46359746-46359761 chr21:46359861-46359876
10	MAX	chr21:46359638-46360586	NB4	blood:	n/a	chr21:46360118-46360128
11	ZNF263	chr21:46359023-46360700	HEK293-T-REx	kidney:	n/a	n/a
12	MYC	chr21:46359272-46360588	K562	blood:	n/a	chr21:46360118-46360128
13	MAZ	chr21:46359485-46360568	IMR90	lung:	n/a	chr21:46360118-46360128
14	IRF1	chr21:46359588-46360715	K562	blood:	n/a	n/a
15	MYC	chr21:46359389-46360610	K562	blood:	n/a	chr21:46360118-46360128
16	BHLHE40	chr21:46359595-46360709	GM12878	blood:	n/a	chr21:46359872-46359888 chr21:46359830-46359846 chr21:46359881-46359897
17	MYC	chr21:46360528-46361127	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr21:46358340-46360742	GM12891	blood:	n/a	n/a
19	CHD1	chr21:46360384-46360692	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr21:46358692-46360738	K562	blood:	n/a	n/a
21	HCFC1	chr21:46359390-46360589	Hela-S3	cervix:	n/a	n/a
22	MYC	chr21:46359376-46360701	MCF10A-Er-Src	breast:	n/a	chr21:46360118-46360128
23	POLR2A	chr21:46358415-46360873	MCF10A-Er-Src	breast:	n/a	n/a
24	MYC	chr21:46359561-46360798	K562	blood:	n/a	chr21:46360118-46360128
25	E2F4	chr21:46359089-46360584	MCF10A-Er-Src	breast:	n/a	chr21:46360122-46360132 chr21:46359882-46359892
26	MXI1	chr21:46359109-46361016	IMR90	lung:	n/a	n/a
27	HDAC2	chr21:46359225-46360616	MCF-7	breast:	n/a	n/a
28	POLR2A	chr21:46358595-46360600	HepG2	liver:	n/a	n/a
29	POLR2A	chr21:46356473-46360821	MCF10A-Er-Src	breast:	n/a	n/a
30	MAX	chr21:46359386-46360666	MCF-7	breast:	n/a	chr21:46360118-46360128
31	POLR2A	chr21:46359542-46360574	Raji	blood:	n/a	n/a
32	MAX	chr21:46359273-46360614	ECC-1	luminal epithelium:	n/a	chr21:46360118-46360128
33	MAX	chr21:46358878-46360665	MCF-7	breast:	n/a	chr21:46360118-46360128
34	MAX	chr21:46359408-46360567	H1-hESC	embryonic stem cell:	n/a	chr21:46360118-46360128
35	SIN3AK20	chr21:46359403-46360838	MCF-7	breast:	n/a	n/a
36	MAX	chr21:46359434-46360569	SK-N-SH	brain:	n/a	chr21:46360118-46360128
37	POLR2A	chr21:46359410-46360707	PBDE	blood:	n/a	n/a
38	SIN3A	chr21:46359585-46360615	H1-hESC	embryonic stem cell:	n/a	chr21:46360114-46360127 chr21:46360350-46360363
39	GABPA	chr21:46359218-46360799	MCF-7	breast:	n/a	chr21:46359828-46359842

No.	Distal block	Cell Line	Cell type
1	chr21:46348854..46378176-chr21:46489799..46500436,75	K562	blood:
2	chr21:46359964..46363434-chr21:46389610..46392494,4	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	chr21:46153888..46156616-chr21:46360093..46361664,2	MCF-7	breast:
8	chr21:46353923..46356909-chr21:46357554..46361249,6	K562	blood:
9	chr21:46236285..46239693-chr21:46357237..46360614,5	K562	blood:
10	chr21:46360355..46363434-chr21:46390613..46392494,3	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
C21orf67	TF binding region
ENSG00000236519	Chromatin interaction
ENSG00000197381	Chromatin interaction
ENSG00000160256	Chromatin interaction
ENSG00000272825	Chromatin interaction
ENSG00000184900	Chromatin interaction
ENSG00000184787	Chromatin interaction
ENSG00000183255	Chromatin interaction
ENSG00000235374	Chromatin interaction
ENSG00000268856	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10775679	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11088970	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11088972	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11088973	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11701017	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11701173	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11701737	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12106389	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12626600	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13046102	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2294169	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2838749	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3827260	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4818745	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4818989	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4818991	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4818992	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4818998	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4819000	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56122469	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7277732	0.92[EUR][1000 genomes]
rs7278544	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7278847	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7283236	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9974072	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9974152	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9974593	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9976402	0.94[AMR][1000 genomes];0.98[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
rs56199687	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	chr21:46358800-46360600	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr21:46358800-46360800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr21:46358800-46361000	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr21:46359000-46361000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr21:46359000-46361000	Active TSS	Fetal Kidney	kidney
6	chr21:46359000-46361200	Active TSS	A549	lung
7	chr21:46359000-46361600	Active TSS	H9 Cell Line	embryonic stem cell
8	chr21:46359000-46361600	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr21:46359200-46360600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr21:46359200-46360600	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr21:46359200-46360800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr21:46359200-46360800	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr21:46359200-46360800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr21:46359200-46360800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
15	chr21:46359200-46361000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr21:46359200-46361000	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr21:46359200-46361000	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr21:46359200-46361200	Active TSS	Psoas Muscle	Psoas
19	chr21:46359200-46361200	Active TSS	GM12878-XiMat	blood
20	chr21:46359200-46361400	Active TSS	Left Ventricle	heart
21	chr21:46359200-46361400	Active TSS	HSMMtube	muscle
22	chr21:46359400-46360600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr21:46359400-46360600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr21:46359400-46360600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr21:46359400-46360600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr21:46359400-46360600	Active TSS	Brain Angular Gyrus	brain
27	chr21:46359400-46360600	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr21:46359400-46360600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr21:46359400-46360600	Active TSS	Brain Substantia Nigra	brain
30	chr21:46359400-46360600	Active TSS	Colon Smooth Muscle	Colon
31	chr21:46359400-46360600	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr21:46359400-46360600	Active TSS	Fetal Heart	heart
33	chr21:46359400-46360600	Active TSS	Fetal Stomach	stomach
34	chr21:46359400-46360600	Active TSS	Gastric	stomach
35	chr21:46359400-46360600	Active TSS	Lung	lung
36	chr21:46359400-46360600	Active TSS	Placenta Amnion	Placenta Amnion
37	chr21:46359400-46360600	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr21:46359400-46360600	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr21:46359400-46360600	Active TSS	Rectal Smooth Muscle	rectum
40	chr21:46359400-46360600	Active TSS	Small Intestine	intestine
41	chr21:46359400-46360600	Active TSS	Thymus	Thymus
42	chr21:46359400-46360600	Active TSS	Hela-S3	cervix
43	chr21:46359400-46360600	Active TSS	NHLF	lung
44	chr21:46359400-46360800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr21:46359400-46360800	Active TSS	H1 Cell Line	embryonic stem cell
46	chr21:46359400-46360800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr21:46359400-46360800	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr21:46359400-46360800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr21:46359400-46360800	Active TSS	Aorta	Aorta
50	chr21:46359400-46360800	Active TSS	Fetal Intestine Large	intestine

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