Variant report

Variant	nsv913402
Chromosome Location	chr21:15545350-15606128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:166)
CpG islands
(count:733)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:166 , 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	ATF1	chr21:15580497-15580694	K562	blood:	n/a	n/a
3	BACH1	chr21:15588533-15589188	H1-hESC	embryonic stem cell:	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	chr21:15592805-15593066	A549	lung:	n/a	chr21:15592892-15592903 chr21:15592876-15592893
8	CEBPB	chr21:15564243-15564490	HepG2	liver:	n/a	n/a
9	CEBPB	chr21:15592776-15593079	HepG2	liver:	n/a	chr21:15592892-15592903 chr21:15592876-15592893
10	CEBPB	chr21:15551618-15551892	K562	blood:	n/a	chr21:15551765-15551776
11	CEBPB	chr21:15551599-15551922	HepG2	liver:	n/a	chr21:15551765-15551776
12	CEBPB	chr21:15564324-15564478	A549	lung:	n/a	n/a
13	CEBPB	chr21:15551684-15551869	A549	lung:	n/a	chr21:15551765-15551776
14	CEBPB	chr21:15551610-15551932	IMR90	lung:	n/a	chr21:15551765-15551776
15	CHD2	chr21:15588506-15588628	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr21:15588115-15588117	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr21:15588477-15588507	K562	blood:	n/a	n/a
18	CTCF	chr21:15588296-15588354	MCF-7	breast:	n/a	n/a
19	CTCF	chr21:15588240-15588390	GM12865	blood:	n/a	n/a
20	CTCF	chr21:15588260-15588410	HRE	kidney:	n/a	n/a
21	CTCF	chr21:15559360-15559510	NB4	blood:	n/a	n/a
22	CTCF	chr21:15588320-15588470	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr21:15588400-15588550	SAEC	small airway:	n/a	n/a
24	CTCF	chr21:15596900-15597099	GM12878	blood:	n/a	chr21:15596974-15596995
25	CTCF	chr21:15588280-15588430	NHEK	skin:	n/a	n/a
26	CTCF	chr21:15588291-15588397	MCF-7	breast:	n/a	n/a
27	CTCF	chr21:15588260-15588410	MCF-7	breast:	n/a	n/a
28	CTCF	chr21:15588255-15588484	Spleen_OC	spleen:	n/a	n/a
29	CUX1	chr21:15583059-15583084	GM12878	blood:	n/a	n/a
30	CUX1	chr21:15563190-15563259	K562	blood:	n/a	n/a
31	E2F4	chr21:15588247-15588565	MCF10A-Er-Src	breast:	n/a	chr21:15588435-15588445
32	E2F4	chr21:15578072-15578319	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr21:15588851-15588925	MCF10A-Er-Src	breast:	n/a	n/a
34	EGR1	chr21:15588181-15588601	H1-hESC	embryonic stem cell:	n/a	chr21:15588308-15588315 chr21:15588345-15588352
35	EGR1	chr21:15588242-15588578	K562	blood:	n/a	chr21:15588308-15588315 chr21:15588345-15588352
36	EGR1	chr21:15588205-15588597	K562	blood:	n/a	chr21:15588308-15588315 chr21:15588345-15588352
37	ELF1	chr21:15588333-15588950	GM12878	blood:	n/a	chr21:15588677-15588689
38	ELF1	chr21:15588275-15588472	K562	blood:	n/a	n/a
39	EP300	chr21:15589387-15589448	GM12878	blood:	n/a	n/a
40	EP300	chr21:15582718-15582879	GM12878	blood:	n/a	n/a
41	EP300	chr21:15584738-15584740	K562	blood:	n/a	n/a
42	ESR1	chr21:15599127-15599629	T-47D	breast:	n/a	n/a
43	FAM48A	chr21:15550031-15550329	GM12878	blood:	n/a	n/a
44	FOS	chr21:15584865-15584954	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr21:15564198-15564371	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr21:15564180-15564380	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr21:15564193-15564401	MCF10A-Er-Src	breast:	n/a	n/a
48	FOXP2	chr21:15588219-15588561	PFSK-1	brain:	n/a	n/a
49	GTF2F1	chr21:15588828-15589012	H1-hESC	embryonic stem cell:	n/a	n/a
50	GTF2F1	chr21:15583242-15583436	H1-hESC	embryonic stem cell:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15588571-15588621	ovcar-3	ovarian:	n/a
2	chr21:15588571-15588621	ovcar-3	ovarian:	n/a
3	chr21:15588608-15588658	HUVEC	blood vessel:	n/a
4	chr21:15588349-15588399	PFSK-1	brain:	n/a
5	chr21:15587812-15587862	HIPEpiC	eye:	n/a
6	chr21:15588372-15588422	HRPEpiC	eye:	n/a
7	chr21:15588349-15588399	GM12892	blood:	n/a
8	chr21:15588571-15588621	MCF-7	breast:	n/a
9	chr21:15588349-15588399	Caco-2	colon:	n/a
10	chr21:15588830-15588880	GM12892	blood:	n/a
11	chr21:15588608-15588658	U87	brain:	n/a
12	chr21:15588349-15588399	ECC-1	luminal epithelium:	n/a
13	chr21:15588848-15588898	SK-N-SH	brain:	n/a
14	chr21:15580581-15580631	PANC-1	pancreas:	n/a
15	chr21:15588372-15588422	ProgFib	skin:	n/a
16	chr21:15580581-15580631	HIPEpiC	eye:	n/a
17	chr21:15588038-15588088	IMR90	lung:	fetal
18	chr21:15588608-15588658	HepG2	liver:	n/a
19	chr21:15588372-15588422	Hela-S3	cervix:	n/a
20	chr21:15588363-15588413	NHBE	bronchial:	n/a
21	chr21:15588608-15588658	SK-N-MC	brain:	n/a
22	chr21:15588038-15588088	SK-N-MC	brain:	n/a
23	chr21:15588363-15588413	MCF-7	breast:	n/a
24	chr21:15580581-15580631	ovcar-3	ovarian:	n/a
25	chr21:15587812-15587862	HNPCEpiC	eye:	n/a
26	chr21:15588571-15588621	HCM	heart:	n/a
27	chr21:15588571-15588621	SK-N-SH_RA	brain:	n/a
28	chr21:15588363-15588413	GM12891	blood:	n/a
29	chr21:15589441-15589491	HPAEpiC	pulmonary alveolar:	n/a
30	chr21:15588830-15588880	ECC-1	luminal epithelium:	n/a
31	chr21:15587812-15587862	HMEC	breast:	n/a
32	chr21:15588848-15588898	T-47D	breast:	n/a
33	chr21:15588608-15588658	Jurkat	blood:	n/a
34	chr21:15588830-15588880	HCF	heart:	n/a
35	chr21:15580581-15580631	U87	brain:	n/a
36	chr21:15580581-15580631	IMR90	lung:	fetal
37	chr21:15588571-15588621	HL-60	blood:	n/a
38	chr21:15588038-15588088	SK-N-SH_RA	brain:	n/a
39	chr21:15587812-15587862	A549	lung:	n/a
40	chr21:15588349-15588399	A549	lung:	n/a
41	chr21:15588848-15588898	HEEpiC	esophagus:	n/a
42	chr21:15588848-15588898	MCF10A-Er-Src	breast:	n/a
43	chr21:15588363-15588413	HCM	heart:	n/a
44	chr21:15588038-15588088	AG09319	gingival:	n/a
45	chr21:15588608-15588658	AG04450	lung:	fetal
46	chr21:15588372-15588422	AG09309	skin:	n/a
47	chr21:15587812-15587862	HEK293	kidney:	embryo
48	chr21:15588349-15588399	HNPCEpiC	eye:	n/a
49	chr21:15588848-15588898	HUVEC	blood vessel:	n/a
50	chr21:15588830-15588880	AG04450	lung:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15591982..15594612-chr21:15596999..15599183,2	K562	blood:
2	chr21:15576826..15579345-chr21:15583403..15585435,2	K562	blood:
3	chr21:15584053..15586326-chr21:15587304..15590158,2	K562	blood:
4	chr21:15591982..15594612-chr21:15596999..15599183,2	K562	blood:
5	chr21:15572112..15574456-chr21:15577631..15579440,2	K562	blood:
6	chr21:15590624..15592860-chr21:15594760..15596779,2	K562	blood:

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
ENSG00000185272	chromatin interactions
ENSG00000188992	chromatin interactions

Extended variants
information (count: 1017 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1017 , 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	rs71315763	chr21:15545413-15545414	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs561118522	chr21:15545414-15545415	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs377148324	chr21:15545454-15545455	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs529200305	chr21:15545457-15545458	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs548961632	chr21:15545473-15545474	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs186566523	chr21:15545478-15545479	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs191447587	chr21:15545485-15545486	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs553302772	chr21:15545486-15545487	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs370582176	chr21:15545490-15545491	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs112278281	chr21:15545530-15545531	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs113235923	chr21:15545545-15545546	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs533647001	chr21:15545565-15545566	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs141531603	chr21:15545592-15545593	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs369741684	chr21:15545612-15545613	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs373495655	chr21:15545693-15545694	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs555477430	chr21:15545698-15545699	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs145694028	chr21:15545703-15545704	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs181651622	chr21:15545714-15545715	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs115899878	chr21:15545741-15545742	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs545648419	chr21:15545746-15545747	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs559171293	chr21:15545780-15545781	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs147742226	chr21:15545781-15545782	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs112749247	chr21:15561819-15561820	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs145583567	chr21:15561827-15561828	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374033060	chr21:15562570-15562571	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs556303096	chr21:15562605-15562606	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs381199	chr21:15562655-15562656	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs200411488	chr21:15562665-15562666	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs544984207	chr21:15562689-15562690	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs539423853	chr21:15562693-15562694	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs559868132	chr21:15563021-15563022	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs377641571	chr21:15563063-15563064	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs138310088	chr21:15563068-15563069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs77043110	chr21:15563094-15563095	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs369742071	chr21:15563097-15563098	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs75829186	chr21:15563098-15563099	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs187860486	chr21:15563137-15563138	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs541875773	chr21:15563145-15563146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs9981966	chr21:15563158-15563159	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs527952657	chr21:15563177-15563178	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs371197905	chr21:15563199-15563200	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs548010264	chr21:15563210-15563211	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs114599259	chr21:15563212-15563213	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs147380811	chr21:15564106-15564107	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs75113550	chr21:15564149-15564150	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs540648920	chr21:15564205-15564206	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs561673404	chr21:15564230-15564231	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs78063679	chr21:15564281-15564282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs550359687	chr21:15564313-15564314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs373910335	chr21:15564314-15564315	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15545400-15545600	Active TSS	Hela-S3	cervix
2	chr21:15545400-15545800	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr21:15545600-15545800	Flanking Active TSS	Hela-S3	cervix
4	chr21:15573200-15573400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
5	chr21:15587800-15588000	Bivalent/Poised TSS	Primary B cells from cord blood	blood
6	chr21:15587800-15588000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr21:15587800-15588000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr21:15587800-15588200	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr21:15587800-15588200	Active TSS	Right Ventricle	heart
10	chr21:15587800-15588800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr21:15587800-15589600	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr21:15588000-15588200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr21:15588000-15588200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
14	chr21:15588000-15588200	Flanking Active TSS	Primary hematopoietic stem cells	blood
15	chr21:15588000-15588200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr21:15588000-15588200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr21:15588000-15588200	Enhancers	GM12878-XiMat	blood
18	chr21:15588000-15588400	Enhancers	Primary B cells from peripheral blood	blood
19	chr21:15588000-15588400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr21:15588000-15588400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
21	chr21:15588000-15588400	Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr21:15588000-15588400	Active TSS	Brain Germinal Matrix	brain
23	chr21:15588000-15588600	Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr21:15588000-15588800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr21:15588000-15588800	Active TSS	Primary B cells from cord blood	blood
26	chr21:15588000-15588800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr21:15588000-15588800	Active TSS	Fetal Brain Female	brain
28	chr21:15588000-15588800	Active TSS	Thymus	Thymus
29	chr21:15588000-15589000	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr21:15588000-15589000	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr21:15588000-15589000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr21:15588000-15589000	Active TSS	Breast Myoepithelial Primary Cells	Breast
33	chr21:15588000-15589000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr21:15588000-15589000	Active TSS	Ovary	ovary
35	chr21:15588000-15589200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr21:15588000-15589200	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr21:15588000-15589200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr21:15588000-15589200	Bivalent/Poised TSS	A549	lung
39	chr21:15588000-15589400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr21:15588000-15589400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr21:15588000-15589400	Active TSS	Brain Angular Gyrus	brain
42	chr21:15588000-15589400	Active TSS	Brain Anterior Caudate	brain
43	chr21:15588000-15589600	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr21:15588000-15589600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
45	chr21:15588000-15589600	Active TSS	Brain Cingulate Gyrus	brain
46	chr21:15588000-15589600	Active TSS	Brain Hippocampus Middle	brain
47	chr21:15588000-15589600	Active TSS	Brain Inferior Temporal Lobe	brain
48	chr21:15588000-15589600	Active TSS	Brain Substantia Nigra	brain
49	chr21:15588000-15589600	Active TSS	Pancreatic Islets	Pancreatic Islet
50	chr21:15588000-15589800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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