Variant report

Variant	nsv587959
Chromosome Location	chr21:47589313-47603902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:250)
CpG islands
(count:489)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:250 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr21:47600273-47600541	K562	blood:	n/a	n/a
2	BHLHE40	chr21:47603834-47605107	K562	blood:	n/a	n/a
3	BHLHE40	chr21:47603113-47603416	K562	blood:	n/a	n/a
4	BHLHE40	chr21:47599878-47600783	K562	blood:	n/a	chr21:47600024-47600040
5	BHLHE40	chr21:47602670-47602874	K562	blood:	n/a	n/a
6	CBX3	chr21:47603261-47605256	K562	blood:	n/a	n/a
7	CCNT2	chr21:47599662-47600295	K562	blood:	n/a	n/a
8	CCNT2	chr21:47601111-47601719	K562	blood:	n/a	chr21:47601532-47601541
9	CCNT2	chr21:47603783-47605058	K562	blood:	n/a	n/a
10	CCNT2	chr21:47602103-47602303	K562	blood:	n/a	n/a
11	CCNT2	chr21:47602516-47603574	K562	blood:	n/a	n/a
12	CEBPB	chr21:47603263-47603964	K562	blood:	n/a	n/a
13	CEBPD	chr21:47603229-47604112	K562	blood:	n/a	n/a
14	CHD2	chr21:47600498-47600573	K562	blood:	n/a	n/a
15	CHD2	chr21:47602210-47602336	K562	blood:	n/a	n/a
16	CTCF	chr21:47602491-47602813	K562	blood:	n/a	n/a
17	CTCF	chr21:47590539-47590619	GM10248	blood:	n/a	n/a
18	CTCF	chr21:47593440-47593590	HepG2	liver:	n/a	n/a
19	CTCF	chr21:47602315-47602837	K562	blood:	n/a	n/a
20	CTCF	chr21:47602413-47602773	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr21:47602610-47602670	K562	blood:	n/a	n/a
22	CTCF	chr21:47596508-47596563	GM10248	blood:	n/a	n/a
23	CTCF	chr21:47602387-47602802	K562	blood:	n/a	n/a
24	CTCF	chr21:47603580-47603665	GM10248	blood:	n/a	n/a
25	CTCF	chr21:47595267-47595330	GM20000	blood:	n/a	n/a
26	CTCF	chr21:47603670-47603684	GM10248	blood:	n/a	n/a
27	CTCF	chr21:47599680-47599830	GM12873	blood:	n/a	n/a
28	CTCF	chr21:47597865-47597885	GM13976	blood:	n/a	n/a
29	CTCF	chr21:47590294-47590358	GM10248	blood:	n/a	n/a
30	CTCF	chr21:47602580-47602666	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr21:47603185-47603333	K562	blood:	n/a	chr21:47603201-47603214
32	CTCF	chr21:47590514-47590527	GM13976	blood:	n/a	n/a
33	CTCF	chr21:47590535-47590671	Lung_OC	lung:	n/a	n/a
34	CTCF	chr21:47590390-47590450	GM13976	blood:	n/a	n/a
35	CTCF	chr21:47590271-47590287	GM10248	blood:	n/a	n/a
36	CTCF	chr21:47602520-47602670	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr21:47602470-47602826	K562	blood:	n/a	n/a
38	CTCF	chr21:47602447-47602803	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr21:47602560-47602710	K562	blood:	n/a	n/a
40	CTCFL	chr21:47602540-47602767	K562	blood:	n/a	n/a
41	CTCFL	chr21:47602553-47602755	K562	blood:	n/a	n/a
42	E2F6	chr21:47602509-47602788	K562	blood:	n/a	n/a
43	E2F6	chr21:47603807-47605118	K562	blood:	n/a	n/a
44	E2F6	chr21:47592507-47592691	K562	blood:	n/a	n/a
45	EBF1	chr21:47603427-47603861	GM12878	blood:	n/a	n/a
46	EGR1	chr21:47603099-47603599	K562	blood:	n/a	chr21:47603156-47603180
47	EGR1	chr21:47599858-47600167	K562	blood:	n/a	chr21:47600012-47600021
48	EGR1	chr21:47603176-47603587	K562	blood:	n/a	n/a
49	EGR1	chr21:47603769-47604285	K562	blood:	n/a	n/a
50	EGR1	chr21:47603781-47604213	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47602486-47602536	SK-N-MC	brain:	n/a
2	chr21:47602486-47602536	SK-N-MC	brain:	n/a
3	chr21:47601211-47601261	T-47D	breast:	n/a
4	chr21:47601211-47601261	ECC-1	luminal epithelium:	n/a
5	chr21:47602432-47602482	GM19239	blood:	n/a
6	chr21:47602432-47602482	SK-N-MC	brain:	n/a
7	chr21:47602148-47602198	ProgFib	skin:	n/a
8	chr21:47601150-47601200	SK-N-SH_RA	brain:	n/a
9	chr21:47599972-47600022	SK-N-SH	brain:	n/a
10	chr21:47599972-47600022	NHDF-neo	bronchial:	n/a
11	chr21:47602486-47602536	MCF10A-Er-Src	breast:	n/a
12	chr21:47601047-47601097	HCT-116	colon:	n/a
13	chr21:47602432-47602482	LNCaP	prostate:	n/a
14	chr21:47599972-47600022	HUVEC	blood vessel:	n/a
15	chr21:47601047-47601097	HRE	kidney:	n/a
16	chr21:47602148-47602198	AG04450	lung:	fetal
17	chr21:47599972-47600022	HL-60	blood:	n/a
18	chr21:47599972-47600022	AG04450	lung:	fetal
19	chr21:47601047-47601097	ovcar-3	ovarian:	n/a
20	chr21:47602486-47602536	HepG2	liver:	n/a
21	chr21:47599972-47600022	AoSMC	blood vessel:	n/a
22	chr21:47602432-47602482	PANC-1	pancreas:	n/a
23	chr21:47601047-47601097	IMR90	lung:	fetal
24	chr21:47601211-47601261	LNCaP	prostate:	n/a
25	chr21:47602486-47602536	HRPEpiC	eye:	n/a
26	chr21:47601211-47601261	NHBE	bronchial:	n/a
27	chr21:47602702-47602752	PFSK-1	brain:	n/a
28	chr21:47601150-47601200	AG09309	skin:	n/a
29	chr21:47602432-47602482	Caco-2	colon:	n/a
30	chr21:47601211-47601261	Caco-2	colon:	n/a
31	chr21:47601211-47601261	NB4	blood:	n/a
32	chr21:47602432-47602482	HIPEpiC	eye:	n/a
33	chr21:47601211-47601261	HL-60	blood:	n/a
34	chr21:47602702-47602752	HCT-116	colon:	n/a
35	chr21:47602486-47602536	HCF	heart:	n/a
36	chr21:47602432-47602482	AG10803	skin:	n/a
37	chr21:47601211-47601261	GM12878	blood:	n/a
38	chr21:47601211-47601261	HRE	kidney:	n/a
39	chr21:47602486-47602536	HRE	kidney:	n/a
40	chr21:47602148-47602198	Hepatocyte	liver:	n/a
41	chr21:47602148-47602198	HCF	heart:	n/a
42	chr21:47601047-47601097	AoSMC	blood vessel:	n/a
43	chr21:47602148-47602198	HCPEpiC	choroid plexus:	n/a
44	chr21:47602432-47602482	GM12878	blood:	n/a
45	chr21:47601150-47601200	SAEC	small airway:	n/a
46	chr21:47599972-47600022	Caco-2	colon:	n/a
47	chr21:47599972-47600022	HCM	heart:	n/a
48	chr21:47602432-47602482	NHDF-neo	bronchial:	n/a
49	chr21:47601047-47601097	NH-A	brain:	n/a
50	chr21:47602148-47602198	GM19239	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47601827..47605045-chr21:47646095..47649627,4	MCF-7	breast:
2	chr21:47540169..47542673-chr21:47591421..47593527,2	MCF-7	breast:
3	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
4	chr21:47601203..47604335-chr21:47632751..47634921,3	K562	blood:
5	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
6	chr21:47571733..47573390-chr21:47601169..47604058,2	K562	blood:
7	chr21:47602595..47605401-chr21:47649000..47651929,3	K562	blood:
8	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
9	chr21:47580435..47582947-chr21:47589052..47590591,2	K562	blood:
10	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
11	chr21:47599873..47602213-chr21:47649234..47651649,2	K562	blood:
12	chr21:47599317..47602217-chr21:47649153..47650672,2	K562	blood:
13	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
14	chr21:47587472..47590076-chr21:47646984..47649833,2	MCF-7	breast:
15	chr21:47598526..47600624-chr21:47604926..47607198,2	K562	blood:
16	chr21:47584368..47587107-chr21:47598667..47601448,3	MCF-7	breast:
17	chr21:47572549..47576001-chr21:47599228..47602499,3	MCF-7	breast:
18	chr21:47568990..47571521-chr21:47602008..47603891,2	K562	blood:
19	chr21:47603167..47605215-chr21:47743246..47745709,3	K562	blood:
20	chr21:47600488..47602703-chr21:47632844..47634921,2	K562	blood:
21	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
22	chr21:47602500..47604164-chr21:47614586..47616622,2	K562	blood:
23	chr21:47600262..47602297-chr21:47602464..47604765,2	K562	blood:
24	chr21:47602452..47604357-chr21:47877079..47880272,3	K562	blood:
25	chr21:47602847..47606841-chr21:47742668..47745795,6	K562	blood:
26	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
27	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
28	chr21:47575014..47577674-chr21:47594867..47597205,2	K562	blood:
29	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
30	chr21:47573796..47576021-chr21:47598325..47600385,2	K562	blood:
31	chr21:47600278..47602930-chr21:47743867..47746831,2	K562	blood:
32	chr21:47563633..47565565-chr21:47603562..47606281,2	K562	blood:
33	chr21:47579510..47581260-chr21:47592233..47594320,2	K562	blood:
34	chr21:47598086..47600168-chr21:47602807..47604710,2	K562	blood:
35	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
36	chr21:47563716..47566123-chr21:47602803..47604796,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000228404	TF binding region
ENSG00000228404	CpG island
ENSG00000160282	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000142173	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000228404	chromatin interactions
ENSG00000160284	chromatin interactions

Extended variants
information (count: 748 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576906332	chr21:47589316-47589317	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs12482756	chr21:47589323-47589324	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs544292328	chr21:47589338-47589339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs12482757	chr21:47589339-47589340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs201106852	chr21:47589348-47589349	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs60164011	chr21:47589352-47589353	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376997332	chr21:47589361-47589362	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562373161	chr21:47589365-47589366	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs12483395	chr21:47589387-47589388	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs58198948	chr21:47589400-47589401	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs377011207	chr21:47589426-47589427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs79990578	chr21:47589438-47589439	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs75801460	chr21:47589439-47589440	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs529629048	chr21:47589442-47589443	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs56950284	chr21:47589463-47589464	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs75121928	chr21:47589465-47589466	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs60024066	chr21:47589477-47589478	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs4572689	chr21:47589478-47589479	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559989897	chr21:47589494-47589495	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs527488435	chr21:47589499-47589500	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs78176367	chr21:47589504-47589505	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs77601477	chr21:47589513-47589514	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs61085157	chr21:47589517-47589518	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs58440454	chr21:47589533-47589534	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs56140752	chr21:47589535-47589536	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs369627221	chr21:47589541-47589542	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs199741547	chr21:47589542-47589543	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112145995	chr21:47589556-47589557	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs564450053	chr21:47589580-47589581	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs77966141	chr21:47589581-47589582	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs369109176	chr21:47589594-47589595	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372669865	chr21:47589618-47589619	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs77188778	chr21:47589632-47589633	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377316965	chr21:47589640-47589641	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs79456057	chr21:47589648-47589649	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs2040286	chr21:47589658-47589659	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs376518898	chr21:47589662-47589663	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs370649592	chr21:47589666-47589667	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs58811436	chr21:47589670-47589671	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs77217483	chr21:47589671-47589672	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs369133924	chr21:47589695-47589696	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs36134401	chr21:47589697-47589698	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs75323049	chr21:47589710-47589711	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs55985429	chr21:47589715-47589716	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372494019	chr21:47589734-47589735	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs562005860	chr21:47589756-47589757	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs35553596	chr21:47589774-47589775	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200624918	chr21:47589812-47589813	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs34157033	chr21:47589825-47589826	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs56324721	chr21:47589826-47589827	Weak transcription	Chromatin interactive region	2 gene(s)	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:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47573400-47590200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr21:47573600-47589600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr21:47573600-47600200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr21:47573600-47602000	Weak transcription	Gastric	stomach
5	chr21:47573800-47590800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr21:47573800-47591400	Weak transcription	Left Ventricle	heart
7	chr21:47573800-47592000	Weak transcription	Right Ventricle	heart
8	chr21:47573800-47593400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr21:47573800-47593400	Weak transcription	Brain Anterior Caudate	brain
10	chr21:47573800-47602200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr21:47573800-47603800	Weak transcription	Right Atrium	heart
12	chr21:47574000-47590400	Weak transcription	Placenta	Placenta
13	chr21:47574200-47590800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr21:47581400-47602800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr21:47581600-47590000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr21:47581600-47600000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr21:47581600-47600200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr21:47582000-47592800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr21:47582000-47602200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr21:47582000-47602800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr21:47582000-47602800	Weak transcription	Ovary	ovary
22	chr21:47582200-47591600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr21:47582400-47600200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr21:47582400-47603800	Weak transcription	Thymus	Thymus
25	chr21:47582600-47592200	Weak transcription	Fetal Intestine Small	intestine
26	chr21:47583000-47602800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr21:47583600-47594000	Weak transcription	Fetal Lung	lung
28	chr21:47583800-47590800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr21:47585800-47592200	Weak transcription	K562	blood
30	chr21:47587400-47589400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr21:47587800-47592200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr21:47588600-47592000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr21:47588600-47592400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr21:47588600-47593600	Weak transcription	Fetal Muscle Leg	muscle
35	chr21:47588600-47599800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr21:47588600-47602800	Weak transcription	Lung	lung
37	chr21:47588800-47590000	Weak transcription	Fetal Stomach	stomach
38	chr21:47588800-47591800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr21:47588800-47592000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr21:47588800-47594000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr21:47589000-47590600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr21:47589000-47591000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr21:47589000-47591000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr21:47589000-47592000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr21:47589000-47600400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr21:47589200-47593400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr21:47589400-47599400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr21:47590000-47592800	Strong transcription	Fetal Stomach	stomach
49	chr21:47590600-47591200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr21:47590600-47591400	Enhancers	Primary T cells fromperipheralblood	blood

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