Variant report

Variant	nsv432145
Chromosome Location	chr21:17559229-17628529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:445)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:17591356-17591655	HepG2	liver:	n/a	n/a
2	BATF	chr21:17571912-17572188	GM12878	blood:	n/a	n/a
3	BCL11A	chr21:17613922-17614292	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr21:17613968-17614230	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr21:17566541-17567013	GM12878	blood:	n/a	n/a
6	BRCA1	chr21:17565274-17565550	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr21:17567880-17568311	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr21:17566254-17567494	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr21:17566241-17567448	Hela-S3	cervix:	n/a	chr21:17567008-17567021
10	CEBPB	chr21:17566343-17566623	IMR90	lung:	n/a	n/a
11	CEBPB	chr21:17565274-17565667	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr21:17569504-17569819	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr21:17613692-17614351	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr21:17565317-17565572	IMR90	lung:	n/a	n/a
15	CEBPB	chr21:17567885-17568148	A549	lung:	n/a	chr21:17568062-17568074
16	CEBPB	chr21:17567885-17568206	IMR90	lung:	n/a	chr21:17568062-17568074 chr21:17568193-17568205
17	CEBPB	chr21:17567838-17568619	Hela-S3	cervix:	n/a	chr21:17568062-17568074 chr21:17568193-17568205
18	CEBPB	chr21:17565247-17565642	A549	lung:	n/a	n/a
19	CEBPB	chr21:17565334-17565604	A549	lung:	n/a	n/a
20	CEBPB	chr21:17565179-17565696	A549	lung:	n/a	n/a
21	CEBPB	chr21:17591389-17591641	HepG2	liver:	n/a	n/a
22	CEBPB	chr21:17565221-17565674	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr21:17565324-17565608	ECC-1	luminal epithelium:	n/a	n/a
24	CHD2	chr21:17565251-17565568	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr21:17566312-17567001	Hela-S3	cervix:	n/a	n/a
26	CREB1	chr21:17567908-17568315	GM12878	blood:	n/a	n/a
27	CREB1	chr21:17567848-17568212	GM12878	blood:	n/a	n/a
28	CTCF	chr21:17566760-17566910	GM12864	blood:	n/a	n/a
29	CTCF	chr21:17566740-17566890	GM12871	blood:	n/a	n/a
30	CTCF	chr21:17566760-17566910	NHLF	lung:	n/a	n/a
31	CTCF	chr21:17583988-17584053	GM10248	blood:	n/a	n/a
32	CTCF	chr21:17566770-17566901	MCF-7	breast:	n/a	n/a
33	CTCF	chr21:17559240-17559390	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr21:17566780-17566930	GM12873	blood:	n/a	n/a
35	CTCF	chr21:17566700-17566850	AG04450	lung:	n/a	n/a
36	CTCF	chr21:17566900-17567050	HAc	cerebellar:	n/a	n/a
37	CTCF	chr21:17566811-17566892	GM12892	blood:	n/a	n/a
38	CTCF	chr21:17614080-17614230	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr21:17566803-17566885	Lung_OC	lung:	n/a	n/a
40	CTCF	chr21:17566746-17566938	Medullo	brain:	n/a	n/a
41	CTCF	chr21:17566698-17566897	HepG2	liver:	n/a	n/a
42	CTCF	chr21:17566780-17566930	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr21:17566720-17566870	HCM	heart:	n/a	n/a
44	CTCF	chr21:17566821-17566837	ProgFib	skin:	n/a	n/a
45	CTCF	chr21:17566636-17567011	GM12878	blood:	n/a	n/a
46	CTCF	chr21:17566780-17566930	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr21:17597580-17597730	HEK293	kidney:	n/a	n/a
48	CTCF	chr21:17566780-17566930	AG04449	skin:	n/a	n/a
49	CTCF	chr21:17614040-17614190	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr21:17613980-17614130	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	chr21:17565450-17565500	SAEC	small airway:	n/a
2	chr21:17565450-17565500	SK-N-SH	brain:	n/a
3	chr21:17565263-17565313	Caco-2	colon:	n/a
4	chr21:17565263-17565313	T-47D	breast:	n/a
5	chr21:17565263-17565313	GM12891	blood:	n/a
6	chr21:17566381-17566431	HCT-116	colon:	n/a
7	chr21:17565450-17565500	ECC-1	luminal epithelium:	n/a
8	chr21:17565263-17565313	BJ	skin:	n/a
9	chr21:17565263-17565313	U87	brain:	n/a
10	chr21:17566381-17566431	Hela-S3	cervix:	n/a
11	chr21:17566381-17566431	CMK	blood:	n/a
12	chr21:17565263-17565313	HepG2	liver:	n/a
13	chr21:17566381-17566431	AG09309	skin:	n/a
14	chr21:17566381-17566431	HRCEpiC	kidney:	n/a
15	chr21:17565263-17565313	RPTEC	kidney:	n/a
16	chr21:17565450-17565500	GM12878	blood:	n/a
17	chr21:17565263-17565313	ovcar-3	ovarian:	n/a
18	chr21:17566381-17566431	MCF-7	breast:	n/a
19	chr21:17566381-17566431	HUVEC	blood vessel:	n/a
20	chr21:17566381-17566431	U87	brain:	n/a
21	chr21:17566381-17566431	Caco-2	colon:	n/a
22	chr21:17566381-17566431	GM12891	blood:	n/a
23	chr21:17565450-17565500	T-47D	breast:	n/a
24	chr21:17565450-17565500	SK-N-SH_RA	brain:	n/a
25	chr21:17565450-17565500	LNCaP	prostate:	n/a
26	chr21:17565263-17565313	Hepatocyte	liver:	n/a
27	chr21:17565263-17565313	HRE	kidney:	n/a
28	chr21:17565263-17565313	NH-A	brain:	n/a
29	chr21:17565263-17565313	PFSK-1	brain:	n/a
30	chr21:17565263-17565313	AG04449	skin:	fetal
31	chr21:17565450-17565500	ovcar-3	ovarian:	n/a
32	chr21:17565450-17565500	GM12892	blood:	n/a
33	chr21:17565263-17565313	HEK293	kidney:	embryo
34	chr21:17565450-17565500	NB4	blood:	n/a
35	chr21:17565263-17565313	HCPEpiC	choroid plexus:	n/a
36	chr21:17566381-17566431	LNCaP	prostate:	n/a
37	chr21:17565263-17565313	IMR90	lung:	fetal
38	chr21:17566381-17566431	AoSMC	blood vessel:	n/a
39	chr21:17565263-17565313	HPAEpiC	pulmonary alveolar:	n/a
40	chr21:17565263-17565313	H1-hESC	embryonic stem cell:	embryo
41	chr21:17565263-17565313	HRPEpiC	eye:	n/a
42	chr21:17565263-17565313	HEEpiC	esophagus:	n/a
43	chr21:17565450-17565500	Hepatocyte	liver:	n/a
44	chr21:17566381-17566431	HRPEpiC	eye:	n/a
45	chr21:17565450-17565500	SK-N-MC	brain:	n/a
46	chr21:17565450-17565500	HL-60	blood:	n/a
47	chr21:17566381-17566431	SK-N-SH_RA	brain:	n/a
48	chr21:17565450-17565500	BE2_C	brain:	n/a
49	chr21:17565450-17565500	HEEpiC	esophagus:	n/a
50	chr21:17566381-17566431	K562	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:89989331..89990190-chr21:17566356..17566935,2	Hela-S3	cervix:
2	chr17:77751904..77752690-chr21:17566657..17567443,2	Hela-S3	cervix:
3	chr21:17552744..17555558-chr21:17617002..17619158,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP25-2	chr21:17566699-17566953	ENSG00000215386
2	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
3	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
4	lnc-USP25-2	chr21:17566788-17566953	ENSG00000215386
5	lnc-USP25-2	chr21:17603376-17603435	NONHSAT081228
6	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386.6
7	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
8	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386.6
9	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386.6
10	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
11	lnc-USP25-2	chr21:17603399-17603435	ENSG00000215386.6
12	lnc-USP25-2	chr21:17566715-17566953	ENSG00000215386.6
13	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386
14	lnc-USP25-2	chr21:17603376-17603435	ENSG00000215386.6
15	lnc-USP25-2	chr21:17566699-17566953	NONHSAT081228

No data

Variant related genes	Relation type
LINC00478	TF binding region
LINC00478	CpG island
ENSG00000258947	chromatin interactions
ENSG00000215386	chromatin interactions
ENSG00000173894	chromatin interactions
CUL5	miRNA target sites
RICH2	miRNA target sites
PLAG1	miRNA target sites
GOLGA4	miRNA target sites

Extended variants
information (count: 2961 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2961 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138586804	chr21:17559331-17559332	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs571894062	chr21:17559347-17559348	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs540866670	chr21:17559411-17559412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561231315	chr21:17559434-17559435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149308584	chr21:17559492-17559493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566784535	chr21:17559512-17559513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535827670	chr21:17559519-17559520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192857544	chr21:17559529-17559530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77510052	chr21:17559534-17559535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184535930	chr21:17559574-17559575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370255538	chr21:17559619-17559620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs202216236	chr21:17559673-17559674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371495316	chr21:17559676-17559677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199648376	chr21:17559677-17559678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548724046	chr21:17559678-17559679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188901338	chr21:17559679-17559680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138131140	chr21:17559694-17559695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547722894	chr21:17559704-17559705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113710975	chr21:17559749-17559750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536554052	chr21:17559782-17559783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550119763	chr21:17559798-17559799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372617877	chr21:17559833-17559834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138338011	chr21:17559882-17559883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs398121457	chr21:17559889-17559890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200300025	chr21:17559890-17559891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145944192	chr21:17559977-17559978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558616434	chr21:17559993-17559994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544828316	chr21:17560003-17560004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572251337	chr21:17560024-17560025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534765957	chr21:17560065-17560066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554473992	chr21:17560106-17560107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200865150	chr21:17560164-17560165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201662285	chr21:17560168-17560169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113323431	chr21:17560174-17560175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71185549	chr21:17560189-17560190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200718730	chr21:17560190-17560191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372033422	chr21:17560193-17560194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200050111	chr21:17560194-17560195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139830444	chr21:17560236-17560237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368835220	chr21:17560256-17560257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576895212	chr21:17560319-17560320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545856283	chr21:17560351-17560352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559489148	chr21:17560389-17560390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528197326	chr21:17560530-17560531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182045148	chr21:17560565-17560566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141190697	chr21:17560577-17560578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550831857	chr21:17560604-17560605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530345044	chr21:17560691-17560692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550190111	chr21:17560749-17560750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2823630	chr21:17560799-17560800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

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	22037309	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17553400-17559800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr21:17553400-17566400	Weak transcription	Fetal Stomach	stomach
3	chr21:17556200-17560400	Enhancers	Brain Cingulate Gyrus	brain
4	chr21:17556400-17559400	Weak transcription	Hela-S3	cervix
5	chr21:17556400-17559600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr21:17557200-17559400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr21:17557200-17559800	Enhancers	Brain Substantia Nigra	brain
8	chr21:17557200-17560400	Enhancers	Brain Hippocampus Middle	brain
9	chr21:17557400-17559600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr21:17557400-17559600	Enhancers	Brain Angular Gyrus	brain
11	chr21:17558000-17559400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr21:17558400-17566400	Weak transcription	Brain Anterior Caudate	brain
13	chr21:17558600-17559600	Enhancers	Rectal Smooth Muscle	rectum
14	chr21:17558600-17560200	Enhancers	Fetal Heart	heart
15	chr21:17558800-17559600	Enhancers	Right Atrium	heart
16	chr21:17559000-17559600	Enhancers	Fetal Lung	lung
17	chr21:17559000-17571200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr21:17559200-17559400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr21:17559200-17559600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr21:17559200-17559600	Enhancers	Placenta	Placenta
21	chr21:17559200-17559600	Enhancers	Ovary	ovary
22	chr21:17559200-17560200	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr21:17559400-17559600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr21:17559400-17560400	Enhancers	Hela-S3	cervix
25	chr21:17559600-17566200	Weak transcription	Ovary	ovary
26	chr21:17559600-17566600	Weak transcription	Placenta	Placenta
27	chr21:17560200-17560400	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr21:17560400-17560800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr21:17563000-17565400	Weak transcription	NHDF-Ad	bronchial
30	chr21:17563200-17563400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr21:17563400-17565200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr21:17563600-17567200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr21:17564600-17566200	Enhancers	Hela-S3	cervix
34	chr21:17565000-17565600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr21:17565200-17565600	Enhancers	Fetal Intestine Large	intestine
36	chr21:17565200-17565800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr21:17565200-17565800	Enhancers	A549	lung
38	chr21:17565200-17566000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr21:17565200-17566200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr21:17565200-17566200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr21:17565200-17566200	Enhancers	Fetal Kidney	kidney
42	chr21:17565200-17566600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr21:17565400-17565600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr21:17565400-17565600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr21:17565400-17565600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr21:17565400-17565600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr21:17565400-17565600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr21:17565400-17565600	Enhancers	Brain Hippocampus Middle	brain
49	chr21:17565400-17565600	Enhancers	Fetal Intestine Small	intestine
50	chr21:17565400-17565600	Enhancers	Thymus	Thymus

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