Variant report

Variant	nsv1065028
Chromosome Location	chr21:17522588-17572535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr21:17571912-17572188	GM12878	blood:	n/a	n/a
2	BCLAF1	chr21:17566541-17567013	GM12878	blood:	n/a	n/a
3	BRCA1	chr21:17565274-17565550	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr21:17566254-17567494	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr21:17567880-17568311	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr21:17541317-17542317	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr21:17567838-17568619	Hela-S3	cervix:	n/a	chr21:17568062-17568074 chr21:17568193-17568205
8	CEBPB	chr21:17541216-17542008	Hela-S3	cervix:	n/a	chr21:17541610-17541621
9	CEBPB	chr21:17565334-17565604	A549	lung:	n/a	n/a
10	CEBPB	chr21:17567885-17568148	A549	lung:	n/a	chr21:17568062-17568074
11	CEBPB	chr21:17552000-17552504	A549	lung:	n/a	chr21:17552093-17552104
12	CEBPB	chr21:17565317-17565572	IMR90	lung:	n/a	n/a
13	CEBPB	chr21:17565247-17565642	A549	lung:	n/a	n/a
14	CEBPB	chr21:17565324-17565608	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr21:17565274-17565667	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr21:17566241-17567448	Hela-S3	cervix:	n/a	chr21:17567008-17567021
17	CEBPB	chr21:17527881-17528085	HepG2	liver:	n/a	n/a
18	CEBPB	chr21:17565221-17565674	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr21:17527846-17528169	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr21:17567885-17568206	IMR90	lung:	n/a	chr21:17568062-17568074 chr21:17568193-17568205
21	CEBPB	chr21:17566343-17566623	IMR90	lung:	n/a	n/a
22	CEBPB	chr21:17541514-17541714	HepG2	liver:	n/a	chr21:17541610-17541621
23	CEBPB	chr21:17527934-17528133	IMR90	lung:	n/a	n/a
24	CEBPB	chr21:17527884-17528160	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr21:17541526-17541842	A549	lung:	n/a	chr21:17541610-17541621
26	CEBPB	chr21:17569504-17569819	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr21:17565179-17565696	A549	lung:	n/a	n/a
28	CHD2	chr21:17565251-17565568	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr21:17566312-17567001	Hela-S3	cervix:	n/a	n/a
30	CREB1	chr21:17567908-17568315	GM12878	blood:	n/a	n/a
31	CREB1	chr21:17567848-17568212	GM12878	blood:	n/a	n/a
32	CTCF	chr21:17566720-17566870	GM12875	blood:	n/a	n/a
33	CTCF	chr21:17566780-17566930	AG10803	skin:	n/a	n/a
34	CTCF	chr21:17566740-17566890	GM06990	blood:	n/a	n/a
35	CTCF	chr21:17566761-17566932	LNCaP	prostate:	n/a	n/a
36	CTCF	chr21:17566736-17566943	A549	lung:	n/a	n/a
37	CTCF	chr21:17566740-17566890	GM12873	blood:	n/a	n/a
38	CTCF	chr21:17566760-17566910	RPTEC	kidney:	n/a	n/a
39	CTCF	chr21:17566820-17566970	HRE	kidney:	n/a	n/a
40	CTCF	chr21:17566811-17566892	GM12892	blood:	n/a	n/a
41	CTCF	chr21:17566820-17566970	GM12869	blood:	n/a	n/a
42	CTCF	chr21:17567320-17567470	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr21:17566780-17566930	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr21:17566780-17566930	AG04449	skin:	n/a	n/a
45	CTCF	chr21:17566720-17566870	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr21:17566803-17566885	Lung_OC	lung:	n/a	n/a
47	CTCF	chr21:17566740-17566890	AG09319	gingival:	n/a	n/a
48	CTCF	chr21:17566800-17566950	GM12873	blood:	n/a	n/a
49	CTCF	chr21:17566760-17566910	AG09309	skin:	n/a	n/a
50	CTCF	chr21:17566780-17566930	HPAF	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:17566381-17566431	AG09309	skin:	n/a
2	chr21:17565263-17565313	SK-N-SH	brain:	n/a
3	chr21:17565450-17565500	MCF-7	breast:	n/a
4	chr21:17565450-17565500	HEK293	kidney:	embryo
5	chr21:17565263-17565313	ECC-1	luminal epithelium:	n/a
6	chr21:17565263-17565313	Caco-2	colon:	n/a
7	chr21:17566381-17566431	NH-A	brain:	n/a
8	chr21:17565450-17565500	SK-N-MC	brain:	n/a
9	chr21:17565263-17565313	U87	brain:	n/a
10	chr21:17566381-17566431	Caco-2	colon:	n/a
11	chr21:17565263-17565313	HCM	heart:	n/a
12	chr21:17565450-17565500	NB4	blood:	n/a
13	chr21:17566381-17566431	K562	blood:	n/a
14	chr21:17565450-17565500	NH-A	brain:	n/a
15	chr21:17566381-17566431	SK-N-MC	brain:	n/a
16	chr21:17565450-17565500	SAEC	small airway:	n/a
17	chr21:17565450-17565500	Caco-2	colon:	n/a
18	chr21:17566381-17566431	HAEpiC	amniotic membrane:	n/a
19	chr21:17566381-17566431	HL-60	blood:	n/a
20	chr21:17565450-17565500	GM12892	blood:	n/a
21	chr21:17565263-17565313	MCF10A-Er-Src	breast:	n/a
22	chr21:17566381-17566431	HEEpiC	esophagus:	n/a
23	chr21:17565450-17565500	HNPCEpiC	eye:	n/a
24	chr21:17566381-17566431	SK-N-SH_RA	brain:	n/a
25	chr21:17565450-17565500	ECC-1	luminal epithelium:	n/a
26	chr21:17566381-17566431	H1-hESC	embryonic stem cell:	embryo
27	chr21:17565263-17565313	GM06990	blood:	n/a
28	chr21:17566381-17566431	PANC-1	pancreas:	n/a
29	chr21:17566381-17566431	GM06990	blood:	n/a
30	chr21:17565450-17565500	BJ	skin:	n/a
31	chr21:17565263-17565313	SK-N-SH_RA	brain:	n/a
32	chr21:17566381-17566431	NHDF-neo	bronchial:	n/a
33	chr21:17565450-17565500	A549	lung:	n/a
34	chr21:17565263-17565313	ovcar-3	ovarian:	n/a
35	chr21:17566381-17566431	MCF-7	breast:	n/a
36	chr21:17565450-17565500	K562	blood:	n/a
37	chr21:17565450-17565500	HRE	kidney:	n/a
38	chr21:17566381-17566431	T-47D	breast:	n/a
39	chr21:17565450-17565500	GM19239	blood:	n/a
40	chr21:17566381-17566431	GM19239	blood:	n/a
41	chr21:17566381-17566431	HPAEpiC	pulmonary alveolar:	n/a
42	chr21:17565263-17565313	GM12891	blood:	n/a
43	chr21:17565450-17565500	CMK	blood:	n/a
44	chr21:17565450-17565500	Jurkat	blood:	n/a
45	chr21:17565263-17565313	HNPCEpiC	eye:	n/a
46	chr21:17565450-17565500	GM06990	blood:	n/a
47	chr21:17566381-17566431	BE2_C	brain:	n/a
48	chr21:17565263-17565313	BJ	skin:	n/a
49	chr21:17565263-17565313	Jurkat	blood:	n/a
50	chr21:17565263-17565313	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:89989331..89990190-chr21:17566356..17566935,2	Hela-S3	cervix:
2	chr17:77751904..77752690-chr21:17566657..17567443,2	Hela-S3	cervix:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP25-2	chr21:17553911-17554007	ENSG00000215386
2	lnc-USP25-2	chr21:17553911-17554007	ENSG00000215386
3	lnc-USP25-2	chr21:17553911-17554007	ENSG00000215386
4	lnc-USP25-2	chr21:17553911-17554007	ENSG00000215386.6
5	lnc-USP25-2	chr21:17566788-17566953	ENSG00000215386
6	lnc-USP25-2	chr21:17553911-17554007	ENSG00000215386.6
7	lnc-USP25-2	chr21:17566699-17566953	ENSG00000215386
8	lnc-USP25-2	chr21:17566715-17566953	ENSG00000215386.6
9	lnc-USP25-2	chr21:17566699-17566953	NONHSAT081228
10	lnc-USP25-2	chr21:17553911-17554007	ENSG00000215386.6

No data

Variant related genes	Relation type
LINC00478	TF binding region
LINC00478	CpG island
ENSG00000173894	chromatin interactions
ENSG00000258947	chromatin interactions
GLCCI1	miRNA target sites
COLEC12	miRNA target sites
CLIP4	miRNA target sites
PLAG1	miRNA target sites

Extended variants
information (count: 1996 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1996 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188981294	chr21:17522606-17522607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530945652	chr21:17522609-17522610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550339617	chr21:17522648-17522649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557017897	chr21:17522664-17522665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111500221	chr21:17522694-17522695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149203436	chr21:17522742-17522743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144902539	chr21:17522743-17522744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546587552	chr21:17522745-17522746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566418279	chr21:17522772-17522773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192930128	chr21:17522776-17522777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370292138	chr21:17522798-17522799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs367930169	chr21:17522811-17522812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs57565342	chr21:17522812-17522813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111571262	chr21:17522813-17522814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184700707	chr21:17522821-17522822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575396333	chr21:17522823-17522824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147965592	chr21:17522827-17522828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557530192	chr21:17522830-17522831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577373109	chr21:17522831-17522832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546426712	chr21:17522843-17522844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4818253	chr21:17522844-17522845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572867089	chr21:17522854-17522855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541804244	chr21:17522868-17522869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561774171	chr21:17522873-17522874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374826436	chr21:17522880-17522881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544340397	chr21:17522886-17522887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200121922	chr21:17522895-17522896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532987182	chr21:17522897-17522898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376225448	chr21:17522903-17522904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369358850	chr21:17522904-17522905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371989409	chr21:17522909-17522910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548980558	chr21:17522921-17522922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4818254	chr21:17522929-17522930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4818255	chr21:17522932-17522933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557567956	chr21:17522936-17522937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4818256	chr21:17522947-17522948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4818257	chr21:17522953-17522954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4818258	chr21:17522982-17522983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372547569	chr21:17523005-17523006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539659334	chr21:17523038-17523039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553564262	chr21:17523044-17523045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545789073	chr21:17523047-17523048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542163250	chr21:17523064-17523065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555331757	chr21:17523126-17523127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575243460	chr21:17523131-17523132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544648030	chr21:17523154-17523155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375573735	chr21:17523158-17523159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559660995	chr21:17523160-17523161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370146248	chr21:17523168-17523169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373322903	chr21:17523175-17523176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Epilepsy	20502679	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	20409316	CNVD
Gastric cancer	18160780	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17518200-17526800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr21:17522600-17526600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr21:17526000-17528400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr21:17526600-17526800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr21:17526600-17527200	Enhancers	Brain Germinal Matrix	brain
6	chr21:17526800-17527200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr21:17526800-17527200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr21:17526800-17527200	Enhancers	Brain Anterior Caudate	brain
9	chr21:17526800-17527800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr21:17526800-17528000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr21:17526800-17528000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr21:17526800-17528000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr21:17526800-17528200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr21:17526800-17528200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr21:17526800-17528400	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr21:17527000-17527800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr21:17527000-17528200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr21:17527000-17528200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr21:17527000-17528400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr21:17527200-17528000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr21:17527200-17553000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr21:17527400-17527800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr21:17528400-17528800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr21:17528400-17535400	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr21:17528800-17529000	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr21:17529000-17540600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr21:17530800-17531200	Enhancers	A549	lung
28	chr21:17530800-17531600	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr21:17530800-17531600	Enhancers	Hela-S3	cervix
30	chr21:17531200-17531400	Flanking Active TSS	A549	lung
31	chr21:17531200-17532000	Enhancers	Osteobl	bone
32	chr21:17531200-17532400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr21:17531400-17531600	Active TSS	A549	lung
34	chr21:17531600-17531800	Flanking Active TSS	A549	lung
35	chr21:17531600-17531800	Flanking Active TSS	Hela-S3	cervix
36	chr21:17531800-17532000	Active TSS	A549	lung
37	chr21:17531800-17532000	Enhancers	Hela-S3	cervix
38	chr21:17532000-17532200	Flanking Active TSS	Hela-S3	cervix
39	chr21:17532000-17532400	Flanking Active TSS	A549	lung
40	chr21:17532000-17532600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr21:17532000-17532600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr21:17532000-17532600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr21:17532200-17532600	Enhancers	Hela-S3	cervix
44	chr21:17532600-17534400	Weak transcription	Hela-S3	cervix
45	chr21:17534800-17535200	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr21:17534800-17535600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr21:17535000-17535400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr21:17535200-17536000	Enhancers	Fetal Kidney	kidney
49	chr21:17535400-17535600	Enhancers	Brain Substantia Nigra	brain
50	chr21:17535400-17535800	Enhancers	Cortex derived primary cultured neurospheres	brain

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