Variant report

Variant	nsv914099
Chromosome Location	chr21:47491014-47548011
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:759)
CpG islands
(count:1527)
Chromatin interactive
region (count:50)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr21:47499588-47499878	GM12878	blood:	n/a	n/a
2	BCL3	chr21:47499620-47499965	GM12878	blood:	n/a	n/a
3	BCL3	chr21:47547814-47548042	GM12878	blood:	n/a	n/a
4	BHLHE40	chr21:47547550-47548181	K562	blood:	n/a	n/a
5	BHLHE40	chr21:47545271-47545435	K562	blood:	n/a	chr21:47545317-47545326
6	BHLHE40	chr21:47516512-47516551	K562	blood:	n/a	n/a
7	BHLHE40	chr21:47503034-47503099	HepG2	liver:	n/a	n/a
8	BHLHE40	chr21:47499569-47499767	K562	blood:	n/a	n/a
9	BHLHE40	chr21:47545687-47545789	K562	blood:	n/a	n/a
10	BHLHE40	chr21:47502920-47503227	K562	blood:	n/a	n/a
11	CBX3	chr21:47528017-47528254	K562	blood:	n/a	n/a
12	CBX3	chr21:47534797-47535280	HCT-116	colon:	n/a	n/a
13	CCNT2	chr21:47517952-47518120	K562	blood:	n/a	n/a
14	CCNT2	chr21:47544395-47544510	K562	blood:	n/a	n/a
15	CEBPB	chr21:47516180-47516208	IMR90	lung:	n/a	n/a
16	CEBPB	chr21:47542272-47542481	IMR90	lung:	n/a	n/a
17	CEBPB	chr21:47520399-47520969	IMR90	lung:	n/a	n/a
18	CEBPB	chr21:47514339-47514541	IMR90	lung:	n/a	n/a
19	CEBPB	chr21:47492417-47492549	HepG2	liver:	n/a	n/a
20	CEBPB	chr21:47511723-47512661	IMR90	lung:	n/a	chr21:47511842-47511855
21	CHD1	chr21:47517617-47521975	IMR90	lung:	n/a	chr21:47518570-47518580 chr21:47518877-47518887
22	CHD2	chr21:47517489-47517580	HepG2	liver:	n/a	n/a
23	CTCF	chr21:47517903-47518136	K562	blood:	n/a	n/a
24	CTCF	chr21:47512840-47512990	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr21:47530968-47531049	Gliobla	brain:	n/a	chr21:47531005-47531023
26	CTCF	chr21:47519380-47519530	AG04450	lung:	n/a	chr21:47519453-47519466
27	CTCF	chr21:47517900-47518050	HRE	kidney:	n/a	n/a
28	CTCF	chr21:47530440-47530590	SK-N-SH_RA	brain:	n/a	chr21:47530508-47530526 chr21:47530510-47530523
29	CTCF	chr21:47513140-47513290	AG10803	skin:	n/a	n/a
30	CTCF	chr21:47519340-47519490	AG10803	skin:	n/a	chr21:47519453-47519466
31	CTCF	chr21:47515380-47515530	K562	blood:	n/a	n/a
32	CTCF	chr21:47517900-47518050	HFF	foreskin:	n/a	n/a
33	CTCF	chr21:47517740-47517890	AG04449	skin:	n/a	chr21:47517795-47517808
34	CTCF	chr21:47519420-47519570	HMF	breast:	n/a	chr21:47519453-47519466
35	CTCF	chr21:47517860-47518010	AG10803	skin:	n/a	n/a
36	CTCF	chr21:47519360-47519510	HepG2	liver:	n/a	chr21:47519453-47519466
37	CTCF	chr21:47517880-47518030	AG09309	skin:	n/a	n/a
38	CTCF	chr21:47515340-47515490	NHEK	skin:	n/a	n/a
39	CTCF	chr21:47519380-47519530	HRE	kidney:	n/a	chr21:47519453-47519466
40	CTCF	chr21:47518640-47518790	AG04449	skin:	n/a	chr21:47518670-47518679
41	CTCF	chr21:47513080-47513230	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr21:47501640-47501790	AG04449	skin:	n/a	n/a
43	CTCF	chr21:47517820-47517970	AG09309	skin:	n/a	n/a
44	CTCF	chr21:47519400-47519550	HA-sp	spinal cord:	n/a	chr21:47519453-47519466
45	CTCF	chr21:47517893-47518058	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr21:47513122-47513230	HepG2	liver:	n/a	n/a
47	CTCF	chr21:47515360-47515510	MCF-7	breast:	n/a	n/a
48	CTCF	chr21:47513140-47513290	AG04450	lung:	n/a	n/a
49	CTCF	chr21:47519580-47519730	NHDF-neo	bronchial:	n/a	chr21:47519621-47519634
50	CTCF	chr21:47517860-47518010	NHLF	lung:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47521576-47521626	HNPCEpiC	eye:	n/a
2	chr21:47517690-47517740	HUVEC	blood vessel:	n/a
3	chr21:47521576-47521626	HNPCEpiC	eye:	n/a
4	chr21:47517690-47517740	HUVEC	blood vessel:	n/a
5	chr21:47518998-47519048	GM19239	blood:	n/a
6	chr21:47530705-47530755	HEEpiC	esophagus:	n/a
7	chr21:47529764-47529814	GM12878	blood:	n/a
8	chr21:47530767-47530817	NHBE	bronchial:	n/a
9	chr21:47518747-47518797	SK-N-SH_RA	brain:	n/a
10	chr21:47518068-47518118	HPAEpiC	pulmonary alveolar:	n/a
11	chr21:47533197-47533247	K562	blood:	n/a
12	chr21:47518998-47519048	HRPEpiC	eye:	n/a
13	chr21:47536647-47536697	GM19239	blood:	n/a
14	chr21:47545624-47545674	SK-N-SH	brain:	n/a
15	chr21:47532333-47532383	HCM	heart:	n/a
16	chr21:47532333-47532383	HMEC	breast:	n/a
17	chr21:47533197-47533247	NHBE	bronchial:	n/a
18	chr21:47517690-47517740	SK-N-SH_RA	brain:	n/a
19	chr21:47545624-47545674	HEK293	kidney:	embryo
20	chr21:47517484-47517534	RPTEC	kidney:	n/a
21	chr21:47536647-47536697	NHDF-neo	bronchial:	n/a
22	chr21:47545200-47545250	HAEpiC	amniotic membrane:	n/a
23	chr21:47545200-47545250	Caco-2	colon:	n/a
24	chr21:47530767-47530817	HPAEpiC	pulmonary alveolar:	n/a
25	chr21:47517484-47517534	GM19239	blood:	n/a
26	chr21:47529764-47529814	MCF-7	breast:	n/a
27	chr21:47544366-47544416	Hela-S3	cervix:	n/a
28	chr21:47541643-47541693	HCM	heart:	n/a
29	chr21:47530767-47530817	ECC-1	luminal epithelium:	n/a
30	chr21:47519444-47519494	PrEC	prostate:	n/a
31	chr21:47532333-47532383	AG09309	skin:	n/a
32	chr21:47545624-47545674	HIPEpiC	eye:	n/a
33	chr21:47541643-47541693	HRE	kidney:	n/a
34	chr21:47518068-47518118	HCF	heart:	n/a
35	chr21:47545200-47545250	SK-N-MC	brain:	n/a
36	chr21:47532820-47532870	H1-hESC	embryonic stem cell:	embryo
37	chr21:47529764-47529814	HPAEpiC	pulmonary alveolar:	n/a
38	chr21:47545624-47545674	H1-hESC	embryonic stem cell:	embryo
39	chr21:47518998-47519048	AG04449	skin:	fetal
40	chr21:47518998-47519048	IMR90	lung:	fetal
41	chr21:47521576-47521626	LNCaP	prostate:	n/a
42	chr21:47545624-47545674	HRE	kidney:	n/a
43	chr21:47532820-47532870	SK-N-SH	brain:	n/a
44	chr21:47530705-47530755	SAEC	small airway:	n/a
45	chr21:47518747-47518797	HCM	heart:	n/a
46	chr21:47546030-47546080	HCT-116	colon:	n/a
47	chr21:47532333-47532383	LNCaP	prostate:	n/a
48	chr21:47515209-47515259	T-47D	breast:	n/a
49	chr21:47531945-47531995	AG04450	lung:	fetal
50	chr21:47530705-47530755	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr21:47538617..47540364-chr21:47544216..47545924,2	K562	blood:
2	chr21:47532415..47535258-chr21:47539694..47542079,2	K562	blood:
3	chr21:47541683..47544429-chr21:47545016..47549303,6	MCF-7	breast:
4	chr21:47528742..47530746-chr21:47548345..47549950,2	K562	blood:
5	chr21:47539891..47541656-chr21:47545952..47548915,2	MCF-7	breast:
6	chr21:47542773..47546170-chr21:47547132..47548940,4	MCF-7	breast:
7	chr21:47537552..47539666-chr21:47543729..47546397,2	MCF-7	breast:
8	chr21:47519810..47521961-chr21:47534620..47537077,2	MCF-7	breast:
9	chr21:47537967..47540415-chr21:47549344..47551448,2	MCF-7	breast:
10	chr21:47498636..47500154-chr21:47500293..47503205,2	MCF-7	breast:
11	chr21:47545773..47548118-chr21:47549714..47552421,3	MCF-7	breast:
12	chr21:47533578..47536250-chr21:47536391..47538002,2	MCF-7	breast:
13	chr21:47493601..47495532-chr21:47497650..47499455,2	K562	blood:
14	chr21:47532227..47535245-chr21:47541514..47543386,3	K562	blood:
15	chr21:47517394..47519929-chr21:47546323..47547843,2	MCF-7	breast:
16	chr21:47513293..47516273-chr21:47516723..47518834,2	K562	blood:
17	chr21:47541436..47543362-chr21:47547811..47549445,2	K562	blood:
18	chr21:47541683..47544429-chr21:47545016..47549303,6	MCF-7	breast:
19	chr21:47518390..47520810-chr21:47533639..47537414,3	MCF-7	breast:
20	chr21:47519810..47521961-chr21:47534620..47537077,2	MCF-7	breast:
21	chr21:47544449..47547894-chr21:47549368..47551933,4	K562	blood:
22	chr21:47547417..47550838-chr21:47552668..47556844,4	K562	blood:
23	chr21:47498636..47500154-chr21:47500293..47503205,2	MCF-7	breast:
24	chr21:47533578..47536250-chr21:47536391..47538002,2	MCF-7	breast:
25	chr21:47490317..47493145-chr21:47513161..47515214,2	K562	blood:
26	chr21:47538006..47540083-chr21:47541061..47544033,2	K562	blood:
27	chr21:47528466..47532989-chr21:47534899..47537069,4	K562	blood:
28	chr21:47547743..47554326-chr21:47559264..47565052,9	K562	blood:
29	chr21:47493601..47495532-chr21:47497650..47499455,2	K562	blood:
30	chr21:47542756..47544736-chr21:47549533..47552490,2	K562	blood:
31	chr21:47542773..47546170-chr21:47547132..47548940,4	MCF-7	breast:
32	chr21:47538006..47540083-chr21:47541061..47544033,2	K562	blood:
33	chr21:47537552..47539666-chr21:47543729..47546397,2	MCF-7	breast:
34	chr21:47541436..47543362-chr21:47547811..47549445,2	K562	blood:
35	chr21:47491970..47494495-chr21:47501163..47503528,2	K562	blood:
36	chr21:47520309..47523211-chr21:47546130..47548721,2	K562	blood:
37	chr21:47393279..47394087-chr21:47517478..47517993,2	K562	blood:
38	chr21:47541862..47543590-chr21:47545123..47546929,2	K562	blood:
39	chr21:47517867..47519980-chr21:47522142..47524798,2	K562	blood:
40	chr21:47507806..47510535-chr21:47515455..47518369,3	K562	blood:
41	chr21:47541862..47543590-chr21:47545123..47546929,2	K562	blood:
42	chr21:47508506..47510114-chr21:47510788..47513094,2	MCF-7	breast:
43	chr21:47532415..47535258-chr21:47539694..47542079,2	K562	blood:
44	chr21:47470351..47471891-chr21:47543505..47546157,2	K562	blood:
45	chr21:47538617..47540364-chr21:47544216..47545924,2	K562	blood:
46	chr21:47485799..47487872-chr21:47511862..47514238,2	K562	blood:
47	chr21:47520309..47523211-chr21:47546130..47548721,2	K562	blood:
48	chr21:47546573..47548982-chr21:47703527..47706476,2	K562	blood:
49	chr21:47508506..47510114-chr21:47510788..47513094,2	MCF-7	breast:
50	chr21:47517867..47520379-chr21:47522142..47524118,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTCD-1	chr21:47517386-47517444	XLOC_014132
2	lnc-FTCD-1	chr21:47513178-47513790	XLOC_014132

No data

Variant related genes	Relation type
ENSG00000227438	TF binding region
PSMA6P3	TF binding region
COL6A2	TF binding region
ENSG00000227438	CpG island
PSMA6P3	CpG island
COL6A2	CpG island
ENSG00000227438	chromatin interactions
ENSG00000160294	chromatin interactions
ENSG00000142173	chromatin interactions
ENSG00000160282	chromatin interactions
ENSG00000233767	chromatin interactions
ENSG00000182362	chromatin interactions

Extended variants
information (count: 3276 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:3276 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8134988	chr21:47491014-47491015	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527354890	chr21:47491042-47491043	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533900741	chr21:47491043-47491044	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552317238	chr21:47491082-47491083	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563911336	chr21:47491087-47491088	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369724188	chr21:47491089-47491090	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549807327	chr21:47491090-47491091	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565005933	chr21:47491095-47491096	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373909654	chr21:47491159-47491160	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56346799	chr21:47491166-47491167	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146544173	chr21:47491200-47491201	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs556499673	chr21:47491211-47491212	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs559035531	chr21:47491214-47491215	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs111843711	chr21:47491226-47491227	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs183684316	chr21:47491227-47491228	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs369911941	chr21:47491228-47491229	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs547354101	chr21:47491234-47491235	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs11700987	chr21:47491264-47491265	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs569825114	chr21:47491273-47491274	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs145028276	chr21:47491279-47491280	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs542562514	chr21:47491290-47491291	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs560636021	chr21:47491296-47491297	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs572712017	chr21:47491300-47491301	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs545893240	chr21:47491332-47491333	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs151301967	chr21:47491339-47491340	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs528065896	chr21:47491357-47491358	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs551404140	chr21:47491370-47491371	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs188200072	chr21:47491386-47491387	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs549711838	chr21:47491387-47491388	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs561549644	chr21:47491398-47491399	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs140532257	chr21:47491435-47491436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547319655	chr21:47491464-47491465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565514324	chr21:47491465-47491466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111934911	chr21:47491487-47491488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556524310	chr21:47491545-47491546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539294903	chr21:47491556-47491557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537193510	chr21:47491605-47491606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552379926	chr21:47491631-47491632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570882905	chr21:47491723-47491724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs193268728	chr21:47491746-47491747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538494769	chr21:47491754-47491755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185442008	chr21:47491758-47491759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375732915	chr21:47491817-47491818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567486989	chr21:47491818-47491819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558614794	chr21:47491829-47491830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188963783	chr21:47491847-47491848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572675742	chr21:47491879-47491880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546462265	chr21:47491902-47491903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558081277	chr21:47491919-47491920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150488180	chr21:47491922-47491923	Weak transcription Enhancers	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:1413 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47485200-47517400	Weak transcription	Right Atrium	heart
2	chr21:47488000-47492000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr21:47488000-47492200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr21:47488000-47498000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr21:47488600-47497600	Weak transcription	NHDF-Ad	bronchial
6	chr21:47489400-47511000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr21:47489600-47499200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr21:47489600-47511000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr21:47491000-47491200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr21:47491000-47492400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr21:47491200-47491400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr21:47491200-47499000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr21:47492000-47492800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr21:47492200-47492600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr21:47492400-47497400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr21:47492600-47494600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr21:47492800-47498400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr21:47494600-47495600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr21:47495600-47497400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr21:47497400-47497600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr21:47497400-47498200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr21:47497600-47497800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr21:47497600-47504800	Enhancers	NHDF-Ad	bronchial
24	chr21:47497800-47498000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr21:47498000-47498400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr21:47498000-47498600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr21:47498000-47498600	Enhancers	Stomach Smooth Muscle	stomach
28	chr21:47498000-47499200	Enhancers	Osteobl	bone
29	chr21:47498200-47499000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr21:47498200-47499400	Enhancers	Adipose Nuclei	Adipose
31	chr21:47498200-47499600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr21:47498200-47500800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr21:47498200-47504600	Enhancers	Fetal Muscle Leg	muscle
34	chr21:47498400-47498600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr21:47498400-47498800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr21:47498400-47499600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
37	chr21:47498400-47499600	Enhancers	NHLF	lung
38	chr21:47498400-47501200	Enhancers	Right Ventricle	heart
39	chr21:47498400-47502000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr21:47498600-47498800	Bivalent Enhancer	Placenta	Placenta
41	chr21:47498600-47498800	Flanking Active TSS	Stomach Smooth Muscle	stomach
42	chr21:47498600-47499000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr21:47498600-47500000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr21:47498600-47500600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr21:47498600-47500600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr21:47498600-47501200	Enhancers	Colon Smooth Muscle	Colon
47	chr21:47498600-47502000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr21:47498800-47499000	Enhancers	Stomach Smooth Muscle	stomach
49	chr21:47498800-47499200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr21:47498800-47500200	Enhancers	Placenta	Placenta

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