Variant report

Variant	rs2227265
Chromosome Location	chr21:45552003-45552004
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:45)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:45 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr21:45551256-45555474	HepG2	liver:	n/a	n/a
2	PML	chr21:45551815-45552580	K562	blood:	n/a	n/a
3	POLR2A	chr21:45551933-45552539	U87	brain:	n/a	n/a
4	POLR2A	chr21:45551223-45554970	PFSK-1	brain:	n/a	n/a
5	POLR2A	chr21:45551345-45553894	PANC-1	pancreas:	n/a	n/a
6	POLR2A	chr21:45551900-45553949	U87	brain:	n/a	n/a
7	POLR2A	chr21:45551860-45552055	A549	lung:	n/a	n/a
8	POLR2A	chr21:45550978-45552667	K562	blood:	n/a	n/a
9	POLR2A	chr21:45551099-45554025	MCF-7	breast:	n/a	n/a
10	POLR2A	chr21:45551276-45552073	HepG2	liver:	n/a	n/a
11	POLR2A	chr21:45550947-45553871	GM12892	blood:	n/a	n/a
12	POLR2A	chr21:45551284-45552224	ECC-1	luminal epithelium:	n/a	n/a
13	POLR2A	chr21:45551623-45552182	GM12878	blood:	n/a	n/a
14	POLR2A	chr21:45551721-45552128	A549	lung:	n/a	n/a
15	POLR2A	chr21:45551055-45552527	GM12891	blood:	n/a	n/a
16	POLR2A	chr21:45551021-45554171	K562	blood:	n/a	n/a
17	POLR2A	chr21:45550936-45556141	PFSK-1	brain:	n/a	n/a
18	CHD2	chr21:45551630-45552173	K562	blood:	n/a	n/a
19	POLR2A	chr21:45551520-45552372	GM18505	blood:	n/a	n/a
20	POLR2A	chr21:45551615-45552594	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr21:45551156-45552470	GM12878	blood:	n/a	n/a
22	POLR2A	chr21:45550983-45552705	GM12892	blood:	n/a	n/a
23	POLR2A	chr21:45551549-45552786	GM12892	blood:	n/a	n/a
24	POLR2A	chr21:45551737-45552496	GM12891	blood:	n/a	n/a
25	POLR2A	chr21:45550524-45555784	GM12878	blood:	n/a	n/a
26	POLR2A	chr21:45551403-45552705	K562	blood:	n/a	n/a
27	POLR2A	chr21:45551397-45552051	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr21:45550463-45553791	K562	blood:	n/a	n/a
29	POLR2A	chr21:45550977-45554195	SK-N-MC	brain:	n/a	n/a
30	POLR2A	chr21:45551986-45552399	GM12878	blood:	n/a	n/a
31	POLR2A	chr21:45551038-45552610	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr21:45551003-45552400	GM12878	blood:	n/a	n/a
33	POLR2A	chr21:45551042-45552545	GM12891	blood:	n/a	n/a
34	POLR2A	chr21:45551043-45552467	HL-60	blood:	n/a	n/a
35	POLR2A	chr21:45551200-45552518	K562	blood:	n/a	n/a
36	POLR2A	chr21:45551006-45552761	K562	blood:	n/a	n/a
37	POLR2A	chr21:45550503-45552611	GM12892	blood:	n/a	n/a
38	POLR2A	chr21:45550191-45554297	K562	blood:	n/a	n/a
39	POLR2A	chr21:45550990-45552456	GM12891	blood:	n/a	n/a
40	POLR2A	chr21:45551098-45552367	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr21:45551224-45552309	GM12878	blood:	n/a	n/a
42	POLR2A	chr21:45551963-45552651	SK-N-SH	brain:	n/a	n/a
43	POLR2A	chr21:45550292-45554259	K562	blood:	n/a	n/a
44	POLR2A	chr21:45551850-45552341	Raji	blood:	n/a	n/a
45	POLR2A	chr21:45551090-45552251	MCF-7	breast:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45551285..45553710-chr21:45659921..45662248,2	MCF-7	breast:
2	chr21:45551834..45580791-chr21:45711953..45732193,97	MCF-7	breast:
3	chr21:45525797..45531105-chr21:45550576..45555096,10	MCF-7	breast:
4	chr21:45551760..45557176-chr21:45717626..45723007,13	MCF-7	breast:
5	chr21:45228525..45230832-chr21:45550134..45553031,3	MCF-7	breast:
6	chr21:45551956..45555178-chr21:45594619..45596938,3	MCF-7	breast:
7	chr21:45550802..45552649-chr21:45562821..45564566,2	MCF-7	breast:
8	chr21:45551674..45553396-chr21:45739259..45741235,2	MCF-7	breast:
9	chr21:45551466..45554089-chr21:45749737..45751999,2	MCF-7	breast:
10	chr21:45525708..45535025-chr21:45544493..45558414,30	MCF-7	breast:
11	chr21:45550460..45552468-chr21:45620537..45623485,2	MCF-7	breast:
12	chr21:45549496..45557767-chr21:45717764..45723476,12	K562	blood:

No data

Variant related genes	Relation type
C21orf33	TF binding region
ENSG00000141959	Chromatin interaction
ENSG00000237604	Chromatin interaction
ENSG00000160223	Chromatin interaction
ENSG00000232124	Chromatin interaction
ENSG00000241945	Chromatin interaction
ENSG00000184441	Chromatin interaction
ENSG00000255902	Chromatin interaction
ENSG00000160226	Chromatin interaction
ENSG00000215458	Chromatin interaction
ENSG00000241728	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1005045	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10470253	0.90[YRI][hapmap]
rs11910604	1.00[JPT][hapmap]
rs2020943	0.81[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2071144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2071145	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2838465	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2838470	1.00[CEU][hapmap];0.90[JPT][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2838479	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2838484	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2838487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2838495	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2838497	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2838510	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs28834388	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57812760	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57855582	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60503863	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61689295	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62226718	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62226719	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62226722	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62226723	0.92[EUR][1000 genomes]
rs62226724	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7275501	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7282644	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73909115	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8128926	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs878132	1.00[JPT][hapmap]
rs9284512	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9306170	0.94[YRI][hapmap]
rs9306175	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9974767	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9975436	0.84[EUR][1000 genomes]
rs9977122	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9978109	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9978772	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9979931	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9980021	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9980063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9982695	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs9982907	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9983551	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9983596	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9984328	0.89[YRI][hapmap]
rs9984820	0.90[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:20 , 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	nsv459293	chr21:45415913-45555079	Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv587721	chr21:45415913-45555079	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	nsv913890	chr21:45482950-45603746	Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
9	nsv459294	chr21:45499171-45595060	Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
10	nsv587722	chr21:45499171-45595060	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv913891	chr21:45508561-45588518	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
12	nsv913892	chr21:45508561-45595060	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
13	nsv913893	chr21:45508561-45603746	Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
14	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
15	nsv913895	chr21:45528919-45595060	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS 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 miRNA target site	31 gene(s)	inside rSNPs	diseases
16	nsv913896	chr21:45528919-45603746	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
17	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
18	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
19	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
20	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

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45528200-45552800	Weak transcription	Right Atrium	heart
2	chr21:45528800-45552200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr21:45528800-45552200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr21:45528800-45552400	Weak transcription	Fetal Heart	heart
5	chr21:45528800-45552400	Strong transcription	Fetal Intestine Small	intestine
6	chr21:45528800-45552600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr21:45529400-45552200	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr21:45530000-45552200	Strong transcription	Primary T helper cells PMA-I stimulated	--
9	chr21:45530600-45552600	Weak transcription	Fetal Brain Male	brain
10	chr21:45532600-45552800	Weak transcription	Fetal Kidney	kidney
11	chr21:45533200-45552400	Strong transcription	Fetal Stomach	stomach
12	chr21:45533400-45552200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr21:45533400-45552200	Strong transcription	NHLF	lung
14	chr21:45535200-45552200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr21:45537000-45552200	Strong transcription	Right Ventricle	heart
16	chr21:45539200-45553000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr21:45541000-45552800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr21:45541200-45552800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr21:45542600-45552200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr21:45544200-45552200	Strong transcription	NHEK	skin
21	chr21:45547400-45552200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr21:45547400-45552200	Strong transcription	Fetal Muscle Trunk	muscle
23	chr21:45547400-45552200	Weak transcription	HSMM	muscle
24	chr21:45548000-45552600	Weak transcription	Small Intestine	intestine
25	chr21:45548200-45552200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr21:45548400-45552400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr21:45548400-45552600	Weak transcription	NH-A	brain
28	chr21:45548600-45552600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr21:45548800-45552200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr21:45548800-45552200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr21:45548800-45552400	Weak transcription	Psoas Muscle	Psoas
32	chr21:45549200-45552200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr21:45549200-45552400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr21:45549200-45552400	Weak transcription	HUVEC	blood vessel
35	chr21:45549200-45552600	Weak transcription	Colon Smooth Muscle	Colon
36	chr21:45549200-45553000	Weak transcription	Stomach Mucosa	stomach
37	chr21:45549400-45552200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr21:45549400-45552400	Weak transcription	A549	lung
39	chr21:45549400-45552400	Weak transcription	HMEC	breast
40	chr21:45549400-45552600	Weak transcription	Fetal Lung	lung
41	chr21:45550000-45552200	Weak transcription	GM12878-XiMat	blood
42	chr21:45550200-45552800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr21:45550600-45552200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr21:45550800-45552800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr21:45551000-45552200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr21:45551000-45552400	Weak transcription	Primary B cells from cord blood	blood
47	chr21:45551000-45552400	Weak transcription	Primary T cells from cord blood	blood
48	chr21:45551000-45552400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr21:45551000-45552600	Weak transcription	Rectal Smooth Muscle	rectum
50	chr21:45551200-45552200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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