Variant report

Variant	nsv1056588
Chromosome Location	chr21:15583231-15615520
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:671)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15583357-15583367	HepG2	liver:	n/a	n/a
2	BACH1	chr21:15588533-15589188	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr21:15613395-15613514	K562	blood:	n/a	n/a
4	BHLHE40	chr21:15588525-15588576	K562	blood:	n/a	n/a
5	CBX3	chr21:15601768-15601981	K562	blood:	n/a	n/a
6	CCNT2	chr21:15588227-15588771	K562	blood:	n/a	n/a
7	CEBPB	chr21:15611695-15611913	K562	blood:	n/a	n/a
8	CEBPB	chr21:15592776-15593079	HepG2	liver:	n/a	chr21:15592892-15592903 chr21:15592876-15592893
9	CEBPB	chr21:15607530-15607658	K562	blood:	n/a	chr21:15607615-15607626
10	CEBPB	chr21:15607494-15607721	HepG2	liver:	n/a	chr21:15607615-15607626
11	CEBPB	chr21:15607503-15607779	K562	blood:	n/a	chr21:15607615-15607626
12	CEBPB	chr21:15607480-15607720	H1-hESC	embryonic stem cell:	n/a	chr21:15607615-15607626
13	CEBPB	chr21:15592805-15593066	A549	lung:	n/a	chr21:15592892-15592903 chr21:15592876-15592893
14	CHD1	chr21:15611641-15611773	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr21:15609867-15609958	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr21:15588477-15588507	K562	blood:	n/a	n/a
17	CHD2	chr21:15588115-15588117	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr21:15588506-15588628	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr21:15588320-15588470	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr21:15588400-15588550	SAEC	small airway:	n/a	n/a
21	CTCF	chr21:15588296-15588354	MCF-7	breast:	n/a	n/a
22	CTCF	chr21:15588240-15588390	GM12865	blood:	n/a	n/a
23	CTCF	chr21:15612565-15612608	GM20000	blood:	n/a	n/a
24	CTCF	chr21:15588260-15588410	HRE	kidney:	n/a	n/a
25	CTCF	chr21:15613420-15613570	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr21:15588280-15588430	NHEK	skin:	n/a	n/a
27	CTCF	chr21:15588291-15588397	MCF-7	breast:	n/a	n/a
28	CTCF	chr21:15588260-15588410	MCF-7	breast:	n/a	n/a
29	CTCF	chr21:15596900-15597099	GM12878	blood:	n/a	chr21:15596974-15596995
30	CTCF	chr21:15615360-15615510	GM12868	blood:	n/a	n/a
31	CTCF	chr21:15588255-15588484	Spleen_OC	spleen:	n/a	n/a
32	E2F4	chr21:15588851-15588925	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr21:15588247-15588565	MCF10A-Er-Src	breast:	n/a	chr21:15588435-15588445
34	EGR1	chr21:15588181-15588601	H1-hESC	embryonic stem cell:	n/a	chr21:15588308-15588315 chr21:15588345-15588352
35	EGR1	chr21:15588205-15588597	K562	blood:	n/a	chr21:15588308-15588315 chr21:15588345-15588352
36	EGR1	chr21:15588242-15588578	K562	blood:	n/a	chr21:15588308-15588315 chr21:15588345-15588352
37	ELF1	chr21:15588333-15588950	GM12878	blood:	n/a	chr21:15588677-15588689
38	ELF1	chr21:15613624-15613969	K562	blood:	n/a	chr21:15613804-15613817
39	ELF1	chr21:15588275-15588472	K562	blood:	n/a	n/a
40	EP300	chr21:15613626-15614215	T-47D	breast:	n/a	chr21:15614176-15614190
41	EP300	chr21:15589387-15589448	GM12878	blood:	n/a	n/a
42	EP300	chr21:15584738-15584740	K562	blood:	n/a	n/a
43	EP300	chr21:15613946-15613977	K562	blood:	n/a	n/a
44	ESR1	chr21:15599127-15599629	T-47D	breast:	n/a	n/a
45	FOS	chr21:15584865-15584954	MCF10A-Er-Src	breast:	n/a	n/a
46	FOXA1	chr21:15613721-15614045	T-47D	breast:	n/a	n/a
47	FOXA1	chr21:15613705-15614125	T-47D	breast:	n/a	n/a
48	FOXP2	chr21:15588219-15588561	PFSK-1	brain:	n/a	n/a
49	GATA3	chr21:15613583-15614133	T-47D	breast:	n/a	n/a
50	GATA3	chr21:15613548-15614151	T-47D	breast:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15588830-15588880	K562	blood:	n/a
2	chr21:15589441-15589491	HUVEC	blood vessel:	n/a
3	chr21:15589441-15589491	HRCEpiC	kidney:	n/a
4	chr21:15587812-15587862	Hela-S3	cervix:	n/a
5	chr21:15588830-15588880	HAEpiC	amniotic membrane:	n/a
6	chr21:15588848-15588898	NT2-D1	testis:	n/a
7	chr21:15588349-15588399	GM19239	blood:	n/a
8	chr21:15588038-15588088	GM12878	blood:	n/a
9	chr21:15588608-15588658	A549	lung:	n/a
10	chr21:15587812-15587862	NHDF-neo	bronchial:	n/a
11	chr21:15587812-15587862	NT2-D1	testis:	n/a
12	chr21:15588038-15588088	HAEpiC	amniotic membrane:	n/a
13	chr21:15587812-15587862	HCPEpiC	choroid plexus:	n/a
14	chr21:15588363-15588413	T-47D	breast:	n/a
15	chr21:15588608-15588658	HAEpiC	amniotic membrane:	n/a
16	chr21:15588363-15588413	GM12892	blood:	n/a
17	chr21:15589441-15589491	NHDF-neo	bronchial:	n/a
18	chr21:15588830-15588880	PrEC	prostate:	n/a
19	chr21:15588608-15588658	GM12891	blood:	n/a
20	chr21:15588830-15588880	HMEC	breast:	n/a
21	chr21:15587812-15587862	U87	brain:	n/a
22	chr21:15588608-15588658	LNCaP	prostate:	n/a
23	chr21:15588571-15588621	GM19239	blood:	n/a
24	chr21:15588608-15588658	HPAEpiC	pulmonary alveolar:	n/a
25	chr21:15588038-15588088	AG04449	skin:	fetal
26	chr21:15588120-15588170	HEEpiC	esophagus:	n/a
27	chr21:15588038-15588088	HL-60	blood:	n/a
28	chr21:15588372-15588422	HNPCEpiC	eye:	n/a
29	chr21:15589441-15589491	HepG2	liver:	n/a
30	chr21:15588372-15588422	Hela-S3	cervix:	n/a
31	chr21:15587812-15587862	HCM	heart:	n/a
32	chr21:15588372-15588422	T-47D	breast:	n/a
33	chr21:15588349-15588399	AoSMC	blood vessel:	n/a
34	chr21:15588830-15588880	GM12892	blood:	n/a
35	chr21:15588372-15588422	GM19239	blood:	n/a
36	chr21:15588349-15588399	HIPEpiC	eye:	n/a
37	chr21:15588372-15588422	PrEC	prostate:	n/a
38	chr21:15588363-15588413	MCF10A-Er-Src	breast:	n/a
39	chr21:15588830-15588880	BE2_C	brain:	n/a
40	chr21:15588608-15588658	SAEC	small airway:	n/a
41	chr21:15588363-15588413	PANC-1	pancreas:	n/a
42	chr21:15589441-15589491	SK-N-MC	brain:	n/a
43	chr21:15588349-15588399	HRPEpiC	eye:	n/a
44	chr21:15588038-15588088	HRCEpiC	kidney:	n/a
45	chr21:15588848-15588898	ProgFib	skin:	n/a
46	chr21:15588571-15588621	IMR90	lung:	fetal
47	chr21:15588372-15588422	SKMC	muscle:	n/a
48	chr21:15588608-15588658	K562	blood:	n/a
49	chr21:15587812-15587862	SK-N-SH_RA	brain:	n/a
50	chr21:15588120-15588170	HCM	heart:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15611898..15613509-chr21:15614140..15616953,2	K562	blood:
2	chr21:15584053..15586326-chr21:15587304..15590158,2	K562	blood:
3	chr21:15611898..15613509-chr21:15614140..15616953,2	K562	blood:
4	chr21:15591982..15594612-chr21:15596999..15599183,2	K562	blood:
5	chr21:15612009..15614501-chr21:15615453..15618275,2	K562	blood:
6	chr21:15612009..15614501-chr21:15615453..15618275,2	K562	blood:
7	chr21:15590624..15592860-chr21:15594760..15596779,2	K562	blood:
8	chr21:15591982..15594612-chr21:15596999..15599183,2	K562	blood:
9	chr21:15576826..15579345-chr21:15583403..15585435,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM11-5	chr21:15608527-15608627	NONHSAT081153

No data

Variant related genes	Relation type
LIPI	TF binding region
ABCC13	TF binding region
RBM11	TF binding region
LIPI	CpG island
ABCC13	CpG island
RBM11	CpG island
ENSG00000188992	chromatin interactions
ENSG00000185272	chromatin interactions

Extended variants
information (count: 1157 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1157 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs380272	chr21:15583332-15583333	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539353136	chr21:15583385-15583386	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs181646859	chr21:15583516-15583517	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572351133	chr21:15583536-15583537	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs541217588	chr21:15583605-15583606	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs371195	chr21:15583629-15583630	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs564025249	chr21:15583656-15583657	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs574831859	chr21:15583694-15583695	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543477846	chr21:15583697-15583698	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369608251	chr21:15583706-15583707	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs533071281	chr21:15583751-15583752	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs563669025	chr21:15583778-15583779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs199518991	chr21:15583821-15583822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560557501	chr21:15583822-15583823	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs74462332	chr21:15583837-15583838	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs72037372	chr21:15583838-15583839	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186165087	chr21:15583839-15583840	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532378189	chr21:15583854-15583855	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs190815775	chr21:15583887-15583888	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs111683910	chr21:15583919-15583920	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs17001380	chr21:15583941-15583942	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs370790376	chr21:15583972-15583973	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547567051	chr21:15583978-15583979	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567389791	chr21:15583989-15583990	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185911744	chr21:15584032-15584033	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549594427	chr21:15584093-15584094	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs17001381	chr21:15584096-15584097	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs60198450	chr21:15584150-15584151	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs552213183	chr21:15584151-15584152	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs529059105	chr21:15584166-15584167	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs565993739	chr21:15584182-15584183	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs534894186	chr21:15584184-15584185	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs569296698	chr21:15584264-15584265	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs431859	chr21:15584288-15584289	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs200119843	chr21:15584346-15584347	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs574855289	chr21:15584348-15584349	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs190782525	chr21:15584360-15584361	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs557169669	chr21:15584396-15584397	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs151152349	chr21:15584414-15584415	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs182581289	chr21:15584479-15584480	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs386816401	chr21:15584483-15584484	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs77882420	chr21:15584485-15584486	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs117856928	chr21:15584510-15584511	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs561170546	chr21:15584531-15584532	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs529828130	chr21:15584543-15584544	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs549895710	chr21:15584545-15584546	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs550561223	chr21:15584659-15584660	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs569642164	chr21:15584679-15584680	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs575257928	chr21:15584695-15584696	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs185770200	chr21:15584705-15584706	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15587800-15588000	Bivalent/Poised TSS	Primary B cells from cord blood	blood
2	chr21:15587800-15588000	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr21:15587800-15588000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr21:15587800-15588200	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr21:15587800-15588200	Active TSS	Right Ventricle	heart
6	chr21:15587800-15588800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr21:15587800-15589600	Active TSS	Duodenum Smooth Muscle	Duodenum
8	chr21:15588000-15588200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr21:15588000-15588200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
10	chr21:15588000-15588200	Flanking Active TSS	Primary hematopoietic stem cells	blood
11	chr21:15588000-15588200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr21:15588000-15588200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr21:15588000-15588200	Enhancers	GM12878-XiMat	blood
14	chr21:15588000-15588400	Enhancers	Primary B cells from peripheral blood	blood
15	chr21:15588000-15588400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr21:15588000-15588400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
17	chr21:15588000-15588400	Active TSS	Cortex derived primary cultured neurospheres	brain
18	chr21:15588000-15588400	Active TSS	Brain Germinal Matrix	brain
19	chr21:15588000-15588600	Active TSS	Primary hematopoietic stem cells short term culture	blood
20	chr21:15588000-15588800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr21:15588000-15588800	Active TSS	Primary B cells from cord blood	blood
22	chr21:15588000-15588800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr21:15588000-15588800	Active TSS	Fetal Brain Female	brain
24	chr21:15588000-15588800	Active TSS	Thymus	Thymus
25	chr21:15588000-15589000	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr21:15588000-15589000	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr21:15588000-15589000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr21:15588000-15589000	Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr21:15588000-15589000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr21:15588000-15589000	Active TSS	Ovary	ovary
31	chr21:15588000-15589200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr21:15588000-15589200	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr21:15588000-15589200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr21:15588000-15589200	Bivalent/Poised TSS	A549	lung
35	chr21:15588000-15589400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
36	chr21:15588000-15589400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr21:15588000-15589400	Active TSS	Brain Angular Gyrus	brain
38	chr21:15588000-15589400	Active TSS	Brain Anterior Caudate	brain
39	chr21:15588000-15589600	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr21:15588000-15589600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr21:15588000-15589600	Active TSS	Brain Cingulate Gyrus	brain
42	chr21:15588000-15589600	Active TSS	Brain Hippocampus Middle	brain
43	chr21:15588000-15589600	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr21:15588000-15589600	Active TSS	Brain Substantia Nigra	brain
45	chr21:15588000-15589600	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr21:15588000-15589800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr21:15588200-15588400	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
48	chr21:15588200-15588400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr21:15588200-15588400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr21:15588200-15588400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood

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