Variant report

Variant	esv1835687
Chromosome Location	chr21:47589099-47605335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:578)
CpG islands
(count:977)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:47603955-47605670	K562	blood:	n/a	n/a
2	ATF1	chr21:47604322-47605322	K562	blood:	n/a	n/a
3	BACH1	chr21:47604094-47604170	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr21:47604533-47605159	H1-hESC	embryonic stem cell:	n/a	chr21:47604969-47604983
5	BACH1	chr21:47604648-47604803	K562	blood:	n/a	n/a
6	BACH1	chr21:47600273-47600541	K562	blood:	n/a	n/a
7	BATF	chr21:47604311-47604581	GM12878	blood:	n/a	n/a
8	BATF	chr21:47604305-47604771	GM12878	blood:	n/a	n/a
9	BCL11A	chr21:47604284-47604707	GM12878	blood:	n/a	n/a
10	BCL11A	chr21:47604296-47604778	GM12878	blood:	n/a	n/a
11	BHLHE40	chr21:47604531-47604866	GM12878	blood:	n/a	n/a
12	BHLHE40	chr21:47603113-47603416	K562	blood:	n/a	n/a
13	BHLHE40	chr21:47603834-47605107	K562	blood:	n/a	n/a
14	BHLHE40	chr21:47602670-47602874	K562	blood:	n/a	n/a
15	BHLHE40	chr21:47599878-47600783	K562	blood:	n/a	chr21:47600024-47600040
16	BRCA1	chr21:47604428-47604792	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr21:47604617-47604806	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr21:47604496-47604500	GM12878	blood:	n/a	n/a
19	BRCA1	chr21:47604610-47604804	HepG2	liver:	n/a	n/a
20	CBX3	chr21:47603261-47605256	K562	blood:	n/a	n/a
21	CCNT2	chr21:47603783-47605058	K562	blood:	n/a	n/a
22	CCNT2	chr21:47602516-47603574	K562	blood:	n/a	n/a
23	CCNT2	chr21:47602103-47602303	K562	blood:	n/a	n/a
24	CCNT2	chr21:47599662-47600295	K562	blood:	n/a	n/a
25	CCNT2	chr21:47601111-47601719	K562	blood:	n/a	chr21:47601532-47601541
26	CEBPB	chr21:47604639-47604980	K562	blood:	n/a	chr21:47604860-47604871
27	CEBPB	chr21:47604151-47605207	K562	blood:	n/a	chr21:47604860-47604871
28	CEBPB	chr21:47604611-47605154	K562	blood:	n/a	chr21:47604860-47604871
29	CEBPB	chr21:47603263-47603964	K562	blood:	n/a	n/a
30	CEBPB	chr21:47604664-47604999	H1-hESC	embryonic stem cell:	n/a	chr21:47604860-47604871
31	CEBPB	chr21:47604625-47605036	HepG2	liver:	n/a	chr21:47604860-47604871
32	CEBPB	chr21:47604594-47605069	MCF-7	breast:	n/a	chr21:47604860-47604871
33	CEBPB	chr21:47604600-47605061	Hela-S3	cervix:	n/a	chr21:47604860-47604871
34	CEBPB	chr21:47604671-47605051	IMR90	lung:	n/a	chr21:47604860-47604871
35	CEBPD	chr21:47603229-47604112	K562	blood:	n/a	n/a
36	CEBPZ	chr21:47604298-47604856	HepG2	liver:	n/a	n/a
37	CHD1	chr21:47604225-47604292	GM12878	blood:	n/a	n/a
38	CHD1	chr21:47604847-47605030	GM12878	blood:	n/a	n/a
39	CHD1	chr21:47604719-47604919	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr21:47602210-47602336	K562	blood:	n/a	n/a
41	CHD2	chr21:47603938-47605049	GM12878	blood:	n/a	n/a
42	CHD2	chr21:47604350-47604863	HepG2	liver:	n/a	n/a
43	CHD2	chr21:47604302-47605034	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr21:47604138-47604903	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr21:47600498-47600573	K562	blood:	n/a	n/a
46	CHD2	chr21:47603959-47605020	K562	blood:	n/a	n/a
47	CREB1	chr21:47604524-47605208	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr21:47604538-47605161	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr21:47604132-47605133	GM12878	blood:	n/a	n/a
50	CTCF	chr21:47595267-47595330	GM20000	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:47599972-47600022	HRE	kidney:	n/a
2	chr21:47599972-47600022	HRE	kidney:	n/a
3	chr21:47604361-47604411	LNCaP	prostate:	n/a
4	chr21:47604052-47604102	HCF	heart:	n/a
5	chr21:47604986-47605036	SK-N-MC	brain:	n/a
6	chr21:47605072-47605122	HRPEpiC	eye:	n/a
7	chr21:47604654-47604704	K562	blood:	n/a
8	chr21:47604052-47604102	HL-60	blood:	n/a
9	chr21:47601150-47601200	AG09309	skin:	n/a
10	chr21:47604986-47605036	AG09319	gingival:	n/a
11	chr21:47602148-47602198	HAEpiC	amniotic membrane:	n/a
12	chr21:47601150-47601200	HIPEpiC	eye:	n/a
13	chr21:47601047-47601097	AG09319	gingival:	n/a
14	chr21:47604654-47604704	SK-N-SH_RA	brain:	n/a
15	chr21:47602432-47602482	K562	blood:	n/a
16	chr21:47605174-47605224	Caco-2	colon:	n/a
17	chr21:47602486-47602536	Hepatocyte	liver:	n/a
18	chr21:47601150-47601200	H1-hESC	embryonic stem cell:	embryo
19	chr21:47605174-47605224	HL-60	blood:	n/a
20	chr21:47604654-47604704	Caco-2	colon:	n/a
21	chr21:47605072-47605122	NB4	blood:	n/a
22	chr21:47604986-47605036	SK-N-SH	brain:	n/a
23	chr21:47604166-47604216	GM12878	blood:	n/a
24	chr21:47604654-47604704	HNPCEpiC	eye:	n/a
25	chr21:47602702-47602752	NH-A	brain:	n/a
26	chr21:47602432-47602482	Hepatocyte	liver:	n/a
27	chr21:47602702-47602752	HRE	kidney:	n/a
28	chr21:47602432-47602482	ovcar-3	ovarian:	n/a
29	chr21:47602148-47602198	PANC-1	pancreas:	n/a
30	chr21:47605174-47605224	HCF	heart:	n/a
31	chr21:47602432-47602482	HUVEC	blood vessel:	n/a
32	chr21:47601211-47601261	GM06990	blood:	n/a
33	chr21:47602148-47602198	SKMC	muscle:	n/a
34	chr21:47604986-47605036	GM12891	blood:	n/a
35	chr21:47602148-47602198	ProgFib	skin:	n/a
36	chr21:47602486-47602536	HCPEpiC	choroid plexus:	n/a
37	chr21:47604166-47604216	ProgFib	skin:	n/a
38	chr21:47604986-47605036	HepG2	liver:	n/a
39	chr21:47605174-47605224	HUVEC	blood vessel:	n/a
40	chr21:47602486-47602536	HIPEpiC	eye:	n/a
41	chr21:47601150-47601200	Hela-S3	cervix:	n/a
42	chr21:47604361-47604411	SK-N-MC	brain:	n/a
43	chr21:47601047-47601097	SK-N-SH_RA	brain:	n/a
44	chr21:47604052-47604102	PrEC	prostate:	n/a
45	chr21:47602486-47602536	IMR90	lung:	fetal
46	chr21:47602486-47602536	NB4	blood:	n/a
47	chr21:47602702-47602752	U87	brain:	n/a
48	chr21:47604361-47604411	GM19239	blood:	n/a
49	chr21:47602486-47602536	Jurkat	blood:	n/a
50	chr21:47602148-47602198	HPAEpiC	pulmonary alveolar:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47573796..47576021-chr21:47598325..47600385,2	K562	blood:
2	chr21:47602847..47606841-chr21:47742668..47745795,6	K562	blood:
3	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
4	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
5	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
6	chr21:47575014..47577674-chr21:47594867..47597205,2	K562	blood:
7	chr21:47563716..47566123-chr21:47602803..47604796,2	K562	blood:
8	chr21:47601203..47604335-chr21:47632751..47634921,3	K562	blood:
9	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
10	chr21:47599317..47602217-chr21:47649153..47650672,2	K562	blood:
11	chr21:47600278..47602930-chr21:47743867..47746831,2	K562	blood:
12	chr21:47601827..47605045-chr21:47646095..47649627,4	MCF-7	breast:
13	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
14	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
15	chr21:47580435..47582947-chr21:47589052..47590591,2	K562	blood:
16	chr21:47587472..47590076-chr21:47646984..47649833,2	MCF-7	breast:
17	chr21:47604083..47605836-chr21:47704849..47706499,2	K562	blood:
18	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
19	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
20	chr21:47599873..47602213-chr21:47649234..47651649,2	K562	blood:
21	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
22	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
23	chr21:47572549..47576001-chr21:47599228..47602499,3	MCF-7	breast:
24	chr21:47600488..47602703-chr21:47632844..47634921,2	K562	blood:
25	chr21:47568990..47571521-chr21:47602008..47603891,2	K562	blood:
26	chr21:47602452..47604357-chr21:47877079..47880272,3	K562	blood:
27	chr21:47584368..47587107-chr21:47598667..47601448,3	MCF-7	breast:
28	chr21:47598526..47600624-chr21:47604926..47607198,2	K562	blood:
29	chr21:47598086..47600168-chr21:47602807..47604710,2	K562	blood:
30	chr21:47540169..47542673-chr21:47591421..47593527,2	MCF-7	breast:
31	chr21:47571733..47573390-chr21:47601169..47604058,2	K562	blood:
32	chr21:47602500..47604164-chr21:47614586..47616622,2	K562	blood:
33	chr21:47603167..47605215-chr21:47743246..47745709,3	K562	blood:
34	chr21:47579510..47581260-chr21:47592233..47594320,2	K562	blood:
35	chr21:47600262..47602297-chr21:47602464..47604765,2	K562	blood:
36	chr21:47563633..47565565-chr21:47603562..47606281,2	K562	blood:
37	chr21:47602595..47605401-chr21:47649000..47651929,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL6A2-4	chr21:47604993-47605101	ENSG00000228404.1

No data

Variant related genes	Relation type
SPATC1L	TF binding region
ENSG00000228404	TF binding region
SPATC1L	CpG island
ENSG00000228404	CpG island
ENSG00000142173	chromatin interactions
ENSG00000160299	chromatin interactions
ENSG00000228404	chromatin interactions
ENSG00000160284	chromatin interactions
ENSG00000182362	chromatin interactions
ENSG00000160305	chromatin interactions
ENSG00000160298	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000215424	chromatin interactions
ENSG00000160282	chromatin interactions
ENSG00000160294	chromatin interactions

Extended variants
information (count: 858 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839128	chr21:47589099-47589100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547095031	chr21:47589114-47589115	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs571605187	chr21:47589115-47589116	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs4819211	chr21:47589136-47589137	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs187603423	chr21:47589141-47589142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs141116527	chr21:47589146-47589147	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs536979376	chr21:47589153-47589154	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs9980792	chr21:47589156-47589157	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs9977340	chr21:47589168-47589169	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs540423067	chr21:47589174-47589175	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs367822514	chr21:47589176-47589177	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs199725013	chr21:47589182-47589183	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs76802500	chr21:47589184-47589185	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs28611289	chr21:47589194-47589195	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs71324496	chr21:47589198-47589199	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs75009205	chr21:47589207-47589208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs558631044	chr21:47589212-47589213	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs13047449	chr21:47589233-47589234	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs28442116	chr21:47589246-47589247	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs149498504	chr21:47589247-47589248	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs146917801	chr21:47589254-47589255	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs12482867	chr21:47589272-47589273	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs112163086	chr21:47589276-47589277	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs13047300	chr21:47589284-47589285	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs13046057	chr21:47589285-47589286	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs111808797	chr21:47589290-47589291	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200192221	chr21:47589310-47589311	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs113178145	chr21:47589311-47589312	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576906332	chr21:47589316-47589317	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs12482756	chr21:47589323-47589324	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs544292328	chr21:47589338-47589339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs12482757	chr21:47589339-47589340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs201106852	chr21:47589348-47589349	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs60164011	chr21:47589352-47589353	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs376997332	chr21:47589361-47589362	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562373161	chr21:47589365-47589366	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs12483395	chr21:47589387-47589388	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs58198948	chr21:47589400-47589401	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs377011207	chr21:47589426-47589427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs79990578	chr21:47589438-47589439	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs75801460	chr21:47589439-47589440	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529629048	chr21:47589442-47589443	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs56950284	chr21:47589463-47589464	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs75121928	chr21:47589465-47589466	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs60024066	chr21:47589477-47589478	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs4572689	chr21:47589478-47589479	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs559989897	chr21:47589494-47589495	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs527488435	chr21:47589499-47589500	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs78176367	chr21:47589504-47589505	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs77601477	chr21:47589513-47589514	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:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr21:47588000-47589200	Strong transcription	Fetal Muscle Trunk	muscle
33	chr21:47588600-47592000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr21:47588600-47592400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr21:47588600-47593600	Weak transcription	Fetal Muscle Leg	muscle
36	chr21:47588600-47599800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr21:47588600-47602800	Weak transcription	Lung	lung
38	chr21:47588800-47590000	Weak transcription	Fetal Stomach	stomach
39	chr21:47588800-47591800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr21:47588800-47592000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr21:47588800-47594000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr21:47589000-47590600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr21:47589000-47591000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr21:47589000-47591000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr21:47589000-47592000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr21:47589000-47600400	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr21:47589200-47593400	Weak transcription	Fetal Muscle Trunk	muscle
48	chr21:47589400-47599400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr21:47590000-47592800	Strong transcription	Fetal Stomach	stomach
50	chr21:47590600-47591200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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