Variant report

Variant	esv1836991
Chromosome Location	chr21:47583506-47603902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:268)
CpG islands
(count:549)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr21:47600273-47600541	K562	blood:	n/a	n/a
2	BHLHE40	chr21:47602670-47602874	K562	blood:	n/a	n/a
3	BHLHE40	chr21:47603113-47603416	K562	blood:	n/a	n/a
4	BHLHE40	chr21:47599878-47600783	K562	blood:	n/a	chr21:47600024-47600040
5	BHLHE40	chr21:47603834-47605107	K562	blood:	n/a	n/a
6	CBX3	chr21:47603261-47605256	K562	blood:	n/a	n/a
7	CCNT2	chr21:47601111-47601719	K562	blood:	n/a	chr21:47601532-47601541
8	CCNT2	chr21:47599662-47600295	K562	blood:	n/a	n/a
9	CCNT2	chr21:47602516-47603574	K562	blood:	n/a	n/a
10	CCNT2	chr21:47603783-47605058	K562	blood:	n/a	n/a
11	CCNT2	chr21:47602103-47602303	K562	blood:	n/a	n/a
12	CEBPB	chr21:47584218-47584328	HepG2	liver:	n/a	n/a
13	CEBPB	chr21:47603263-47603964	K562	blood:	n/a	n/a
14	CEBPD	chr21:47603229-47604112	K562	blood:	n/a	n/a
15	CHD2	chr21:47602210-47602336	K562	blood:	n/a	n/a
16	CHD2	chr21:47600498-47600573	K562	blood:	n/a	n/a
17	CTCF	chr21:47599680-47599830	GM12873	blood:	n/a	n/a
18	CTCF	chr21:47602610-47602670	K562	blood:	n/a	n/a
19	CTCF	chr21:47590514-47590527	GM13976	blood:	n/a	n/a
20	CTCF	chr21:47602560-47602710	K562	blood:	n/a	n/a
21	CTCF	chr21:47602413-47602773	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr21:47602387-47602802	K562	blood:	n/a	n/a
23	CTCF	chr21:47602580-47602666	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr21:47590390-47590450	GM13976	blood:	n/a	n/a
25	CTCF	chr21:47590294-47590358	GM10248	blood:	n/a	n/a
26	CTCF	chr21:47602447-47602803	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr21:47597865-47597885	GM13976	blood:	n/a	n/a
28	CTCF	chr21:47595267-47595330	GM20000	blood:	n/a	n/a
29	CTCF	chr21:47602470-47602826	K562	blood:	n/a	n/a
30	CTCF	chr21:47602491-47602813	K562	blood:	n/a	n/a
31	CTCF	chr21:47590271-47590287	GM10248	blood:	n/a	n/a
32	CTCF	chr21:47602315-47602837	K562	blood:	n/a	n/a
33	CTCF	chr21:47590539-47590619	GM10248	blood:	n/a	n/a
34	CTCF	chr21:47590535-47590671	Lung_OC	lung:	n/a	n/a
35	CTCF	chr21:47593440-47593590	HepG2	liver:	n/a	n/a
36	CTCF	chr21:47603185-47603333	K562	blood:	n/a	chr21:47603201-47603214
37	CTCF	chr21:47603670-47603684	GM10248	blood:	n/a	n/a
38	CTCF	chr21:47603580-47603665	GM10248	blood:	n/a	n/a
39	CTCF	chr21:47596508-47596563	GM10248	blood:	n/a	n/a
40	CTCF	chr21:47602520-47602670	WERI-Rb-1	eye:	n/a	n/a
41	CTCFL	chr21:47602553-47602755	K562	blood:	n/a	n/a
42	CTCFL	chr21:47602540-47602767	K562	blood:	n/a	n/a
43	CUX1	chr21:47587940-47588030	K562	blood:	n/a	n/a
44	E2F6	chr21:47602509-47602788	K562	blood:	n/a	n/a
45	E2F6	chr21:47592507-47592691	K562	blood:	n/a	n/a
46	E2F6	chr21:47603807-47605118	K562	blood:	n/a	n/a
47	EBF1	chr21:47603427-47603861	GM12878	blood:	n/a	n/a
48	EGR1	chr21:47599858-47600167	K562	blood:	n/a	chr21:47600012-47600021
49	EGR1	chr21:47603769-47604285	K562	blood:	n/a	n/a
50	EGR1	chr21:47603099-47603599	K562	blood:	n/a	chr21:47603156-47603180

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47601047-47601097	MCF-7	breast:	n/a
2	chr21:47602148-47602198	SK-N-SH	brain:	n/a
3	chr21:47602148-47602198	AG10803	skin:	n/a
4	chr21:47599972-47600022	HepG2	liver:	n/a
5	chr21:47601047-47601097	PANC-1	pancreas:	n/a
6	chr21:47585850-47585900	GM19239	blood:	n/a
7	chr21:47599972-47600022	GM06990	blood:	n/a
8	chr21:47602432-47602482	HRPEpiC	eye:	n/a
9	chr21:47602702-47602752	IMR90	lung:	fetal
10	chr21:47602432-47602482	GM19239	blood:	n/a
11	chr21:47601211-47601261	AoSMC	blood vessel:	n/a
12	chr21:47585850-47585900	HIPEpiC	eye:	n/a
13	chr21:47601150-47601200	NB4	blood:	n/a
14	chr21:47602486-47602536	SK-N-SH_RA	brain:	n/a
15	chr21:47602486-47602536	Caco-2	colon:	n/a
16	chr21:47602486-47602536	MCF-7	breast:	n/a
17	chr21:47602486-47602536	PANC-1	pancreas:	n/a
18	chr21:47602148-47602198	GM12891	blood:	n/a
19	chr21:47601047-47601097	SK-N-MC	brain:	n/a
20	chr21:47602432-47602482	HRE	kidney:	n/a
21	chr21:47601150-47601200	Caco-2	colon:	n/a
22	chr21:47602702-47602752	NHDF-neo	bronchial:	n/a
23	chr21:47602486-47602536	NHDF-neo	bronchial:	n/a
24	chr21:47602432-47602482	LNCaP	prostate:	n/a
25	chr21:47602432-47602482	NHBE	bronchial:	n/a
26	chr21:47601150-47601200	AG04449	skin:	fetal
27	chr21:47585850-47585900	HAEpiC	amniotic membrane:	n/a
28	chr21:47602148-47602198	K562	blood:	n/a
29	chr21:47585850-47585900	HL-60	blood:	n/a
30	chr21:47599972-47600022	HIPEpiC	eye:	n/a
31	chr21:47601211-47601261	NB4	blood:	n/a
32	chr21:47602148-47602198	SAEC	small airway:	n/a
33	chr21:47585850-47585900	Hepatocyte	liver:	n/a
34	chr21:47601211-47601261	GM12892	blood:	n/a
35	chr21:47602148-47602198	NHBE	bronchial:	n/a
36	chr21:47602148-47602198	HEEpiC	esophagus:	n/a
37	chr21:47585850-47585900	NHBE	bronchial:	n/a
38	chr21:47585850-47585900	U87	brain:	n/a
39	chr21:47585850-47585900	LNCaP	prostate:	n/a
40	chr21:47602702-47602752	AG04449	skin:	fetal
41	chr21:47602702-47602752	GM06990	blood:	n/a
42	chr21:47601211-47601261	H1-hESC	embryonic stem cell:	embryo
43	chr21:47601150-47601200	SK-N-SH_RA	brain:	n/a
44	chr21:47602486-47602536	HRE	kidney:	n/a
45	chr21:47601150-47601200	SK-N-MC	brain:	n/a
46	chr21:47601150-47601200	PANC-1	pancreas:	n/a
47	chr21:47602432-47602482	NB4	blood:	n/a
48	chr21:47601047-47601097	GM12891	blood:	n/a
49	chr21:47602148-47602198	HepG2	liver:	n/a
50	chr21:47601211-47601261	HL-60	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47600278..47602930-chr21:47743867..47746831,2	K562	blood:
2	chr21:47572189..47573895-chr21:47587183..47588702,2	K562	blood:
3	chr21:47587472..47590076-chr21:47646984..47649833,2	MCF-7	breast:
4	chr21:47572549..47576001-chr21:47599228..47602499,3	MCF-7	breast:
5	chr21:47602500..47604164-chr21:47614586..47616622,2	K562	blood:
6	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
7	chr21:47579510..47581260-chr21:47592233..47594320,2	K562	blood:
8	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
9	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
10	chr21:47571733..47573390-chr21:47601169..47604058,2	K562	blood:
11	chr21:47583504..47585135-chr21:47586773..47588426,2	K562	blood:
12	chr21:47580435..47582947-chr21:47589052..47590591,2	K562	blood:
13	chr21:47602452..47604357-chr21:47877079..47880272,3	K562	blood:
14	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
15	chr21:47578648..47581560-chr21:47583837..47585987,2	MCF-7	breast:
16	chr21:47579366..47583740-chr21:47600501..47605706,6	K562	blood:
17	chr21:47573796..47576021-chr21:47598325..47600385,2	K562	blood:
18	chr21:47600262..47602297-chr21:47602464..47604765,2	K562	blood:
19	chr21:47602847..47606841-chr21:47742668..47745795,6	K562	blood:
20	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
21	chr21:47601827..47605045-chr21:47646095..47649627,4	MCF-7	breast:
22	chr21:47563716..47566123-chr21:47602803..47604796,2	K562	blood:
23	chr21:47584368..47587107-chr21:47598667..47601448,3	MCF-7	breast:
24	chr21:47599873..47602213-chr21:47649234..47651649,2	K562	blood:
25	chr21:47603167..47605215-chr21:47743246..47745709,3	K562	blood:
26	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
27	chr21:47575014..47577674-chr21:47594867..47597205,2	K562	blood:
28	chr21:47575923..47577951-chr21:47583383..47585806,2	K562	blood:
29	chr21:47598526..47600624-chr21:47604926..47607198,2	K562	blood:
30	chr21:47598086..47600168-chr21:47602807..47604710,2	K562	blood:
31	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
32	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
33	chr21:47602595..47605401-chr21:47649000..47651929,3	K562	blood:
34	chr21:47578880..47581848-chr21:47584809..47588383,3	K562	blood:
35	chr21:47540169..47542673-chr21:47591421..47593527,2	MCF-7	breast:
36	chr21:47568990..47571521-chr21:47602008..47603891,2	K562	blood:
37	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
38	chr21:47583504..47585135-chr21:47586773..47588426,2	K562	blood:
39	chr21:47601203..47604335-chr21:47632751..47634921,3	K562	blood:
40	chr21:47584368..47587107-chr21:47598667..47601448,3	MCF-7	breast:
41	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
42	chr21:47600488..47602703-chr21:47632844..47634921,2	K562	blood:
43	chr21:47599317..47602217-chr21:47649153..47650672,2	K562	blood:
44	chr21:47563633..47565565-chr21:47603562..47606281,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000228404	TF binding region
ENSG00000228404	CpG island
ENSG00000160282	chromatin interactions
ENSG00000228404	chromatin interactions
ENSG00000160284	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000142173	chromatin interactions

Extended variants
information (count: 1024 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12329865	chr21:47583506-47583507	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565528244	chr21:47583507-47583508	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs577493819	chr21:47583511-47583512	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs544332294	chr21:47583552-47583553	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562412191	chr21:47583617-47583618	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs529714944	chr21:47583623-47583624	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs547829045	chr21:47583649-47583650	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs367864529	chr21:47583778-47583779	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372447000	chr21:47583802-47583803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112269275	chr21:47583819-47583820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs60663823	chr21:47583838-47583839	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs544840303	chr21:47583850-47583851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78628163	chr21:47583866-47583867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35258565	chr21:47583902-47583903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542123165	chr21:47583905-47583906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs386819413	chr21:47583915-47583916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs28611479	chr21:47583916-47583917	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs367633510	chr21:47583917-47583918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551075131	chr21:47583935-47583936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190685625	chr21:47583985-47583986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139815919	chr21:47584010-47584011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12329662	chr21:47584020-47584021	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs555040746	chr21:47584050-47584051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573269304	chr21:47584062-47584063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183244834	chr21:47584078-47584079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12329665	chr21:47584090-47584091	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs12329859	chr21:47584104-47584105	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs573884332	chr21:47584123-47584124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373465851	chr21:47584199-47584200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149793501	chr21:47584212-47584213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116085901	chr21:47584214-47584215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12329667	chr21:47584216-47584217	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs541900677	chr21:47584221-47584222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138851955	chr21:47584236-47584237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559743721	chr21:47584252-47584253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117030074	chr21:47584277-47584278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545707234	chr21:47584333-47584334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575283451	chr21:47584341-47584342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564010617	chr21:47584359-47584360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531533642	chr21:47584360-47584361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371289214	chr21:47584466-47584467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549665909	chr21:47584467-47584468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568234166	chr21:47584473-47584474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370993055	chr21:47584498-47584499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62214045	chr21:47584504-47584505	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs140674111	chr21:47584563-47584564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566908016	chr21:47584567-47584568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534152179	chr21:47584574-47584575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559316634	chr21:47584630-47584631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571011135	chr21:47584631-47584632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:36)

Disease	PMID	Source
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	17899364	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47573400-47590200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr21:47573600-47589600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr21:47573600-47600200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr21:47573600-47602000	Weak transcription	Gastric	stomach
5	chr21:47573800-47585400	Weak transcription	Brain Angular Gyrus	brain
6	chr21:47573800-47585600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr21:47573800-47588000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr21:47573800-47590800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr21:47573800-47591400	Weak transcription	Left Ventricle	heart
10	chr21:47573800-47592000	Weak transcription	Right Ventricle	heart
11	chr21:47573800-47593400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr21:47573800-47593400	Weak transcription	Brain Anterior Caudate	brain
13	chr21:47573800-47602200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr21:47573800-47603800	Weak transcription	Right Atrium	heart
15	chr21:47574000-47590400	Weak transcription	Placenta	Placenta
16	chr21:47574200-47590800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr21:47575800-47583800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr21:47580000-47583600	ZNF genes & repeats	K562	blood
19	chr21:47580200-47588000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr21:47581400-47585400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr21:47581400-47602800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr21:47581600-47588000	Weak transcription	Lung	lung
23	chr21:47581600-47588400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr21:47581600-47588800	Weak transcription	Spleen	Spleen
25	chr21:47581600-47590000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr21:47581600-47600000	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr21:47581600-47600200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr21:47581800-47588000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr21:47582000-47585200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr21:47582000-47588000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr21:47582000-47588000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr21:47582000-47592800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr21:47582000-47602200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr21:47582000-47602800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr21:47582000-47602800	Weak transcription	Ovary	ovary
36	chr21:47582200-47588200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr21:47582200-47591600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr21:47582400-47588000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr21:47582400-47588000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr21:47582400-47600200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr21:47582400-47603800	Weak transcription	Thymus	Thymus
42	chr21:47582600-47592200	Weak transcription	Fetal Intestine Small	intestine
43	chr21:47582800-47583600	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr21:47582800-47587400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr21:47583000-47583800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr21:47583000-47587600	Weak transcription	Fetal Muscle Leg	muscle
47	chr21:47583000-47588000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr21:47583000-47602800	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr21:47583200-47584400	Strong transcription	Fetal Stomach	stomach
50	chr21:47583400-47583800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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