Variant report

Variant	esv1824913
Chromosome Location	chr21:47588465-47603973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:270)
CpG islands
(count:489)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:270 , 50 per page) page: 1 2 3 4 5 6

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	BACH1	chr21:47600273-47600541	K562	blood:	n/a	n/a
3	BHLHE40	chr21:47603834-47605107	K562	blood:	n/a	n/a
4	BHLHE40	chr21:47602670-47602874	K562	blood:	n/a	n/a
5	BHLHE40	chr21:47603113-47603416	K562	blood:	n/a	n/a
6	BHLHE40	chr21:47599878-47600783	K562	blood:	n/a	chr21:47600024-47600040
7	CBX3	chr21:47603261-47605256	K562	blood:	n/a	n/a
8	CCNT2	chr21:47602516-47603574	K562	blood:	n/a	n/a
9	CCNT2	chr21:47599662-47600295	K562	blood:	n/a	n/a
10	CCNT2	chr21:47601111-47601719	K562	blood:	n/a	chr21:47601532-47601541
11	CCNT2	chr21:47602103-47602303	K562	blood:	n/a	n/a
12	CCNT2	chr21:47603783-47605058	K562	blood:	n/a	n/a
13	CEBPB	chr21:47603263-47603964	K562	blood:	n/a	n/a
14	CEBPD	chr21:47603229-47604112	K562	blood:	n/a	n/a
15	CHD2	chr21:47603959-47605020	K562	blood:	n/a	n/a
16	CHD2	chr21:47602210-47602336	K562	blood:	n/a	n/a
17	CHD2	chr21:47603938-47605049	GM12878	blood:	n/a	n/a
18	CHD2	chr21:47600498-47600573	K562	blood:	n/a	n/a
19	CTCF	chr21:47602387-47602802	K562	blood:	n/a	n/a
20	CTCF	chr21:47590514-47590527	GM13976	blood:	n/a	n/a
21	CTCF	chr21:47599680-47599830	GM12873	blood:	n/a	n/a
22	CTCF	chr21:47593440-47593590	HepG2	liver:	n/a	n/a
23	CTCF	chr21:47602470-47602826	K562	blood:	n/a	n/a
24	CTCF	chr21:47603185-47603333	K562	blood:	n/a	chr21:47603201-47603214
25	CTCF	chr21:47596508-47596563	GM10248	blood:	n/a	n/a
26	CTCF	chr21:47590539-47590619	GM10248	blood:	n/a	n/a
27	CTCF	chr21:47597865-47597885	GM13976	blood:	n/a	n/a
28	CTCF	chr21:47590390-47590450	GM13976	blood:	n/a	n/a
29	CTCF	chr21:47603580-47603665	GM10248	blood:	n/a	n/a
30	CTCF	chr21:47590535-47590671	Lung_OC	lung:	n/a	n/a
31	CTCF	chr21:47590271-47590287	GM10248	blood:	n/a	n/a
32	CTCF	chr21:47602447-47602803	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr21:47603670-47603684	GM10248	blood:	n/a	n/a
34	CTCF	chr21:47602315-47602837	K562	blood:	n/a	n/a
35	CTCF	chr21:47602413-47602773	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr21:47602610-47602670	K562	blood:	n/a	n/a
37	CTCF	chr21:47595267-47595330	GM20000	blood:	n/a	n/a
38	CTCF	chr21:47602491-47602813	K562	blood:	n/a	n/a
39	CTCF	chr21:47602580-47602666	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr21:47602560-47602710	K562	blood:	n/a	n/a
41	CTCF	chr21:47590294-47590358	GM10248	blood:	n/a	n/a
42	CTCF	chr21:47602520-47602670	WERI-Rb-1	eye:	n/a	n/a
43	CTCFL	chr21:47602540-47602767	K562	blood:	n/a	n/a
44	CTCFL	chr21:47602553-47602755	K562	blood:	n/a	n/a
45	CUX1	chr21:47603946-47604368	K562	blood:	n/a	n/a
46	E2F6	chr21:47592507-47592691	K562	blood:	n/a	n/a
47	E2F6	chr21:47602509-47602788	K562	blood:	n/a	n/a
48	E2F6	chr21:47603807-47605118	K562	blood:	n/a	n/a
49	EBF1	chr21:47603427-47603861	GM12878	blood:	n/a	n/a
50	EGR1	chr21:47603176-47603587	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	chr21:47602702-47602752	HNPCEpiC	eye:	n/a
2	chr21:47602702-47602752	HNPCEpiC	eye:	n/a
3	chr21:47602486-47602536	HAEpiC	amniotic membrane:	n/a
4	chr21:47601047-47601097	HNPCEpiC	eye:	n/a
5	chr21:47601150-47601200	NHBE	bronchial:	n/a
6	chr21:47601047-47601097	ECC-1	luminal epithelium:	n/a
7	chr21:47602702-47602752	BE2_C	brain:	n/a
8	chr21:47601047-47601097	HMEC	breast:	n/a
9	chr21:47602148-47602198	GM12878	blood:	n/a
10	chr21:47602432-47602482	HRE	kidney:	n/a
11	chr21:47602702-47602752	LNCaP	prostate:	n/a
12	chr21:47602486-47602536	AG09319	gingival:	n/a
13	chr21:47599972-47600022	BJ	skin:	n/a
14	chr21:47601211-47601261	ECC-1	luminal epithelium:	n/a
15	chr21:47602432-47602482	MCF-7	breast:	n/a
16	chr21:47599972-47600022	CMK	blood:	n/a
17	chr21:47601150-47601200	HCPEpiC	choroid plexus:	n/a
18	chr21:47601047-47601097	BJ	skin:	n/a
19	chr21:47602148-47602198	AG09319	gingival:	n/a
20	chr21:47602148-47602198	HRCEpiC	kidney:	n/a
21	chr21:47599972-47600022	MCF-7	breast:	n/a
22	chr21:47601211-47601261	HCF	heart:	n/a
23	chr21:47602148-47602198	CMK	blood:	n/a
24	chr21:47601047-47601097	NHDF-neo	bronchial:	n/a
25	chr21:47601211-47601261	MCF-7	breast:	n/a
26	chr21:47602486-47602536	A549	lung:	n/a
27	chr21:47601150-47601200	A549	lung:	n/a
28	chr21:47601211-47601261	GM19239	blood:	n/a
29	chr21:47602148-47602198	A549	lung:	n/a
30	chr21:47602486-47602536	SKMC	muscle:	n/a
31	chr21:47601047-47601097	RPTEC	kidney:	n/a
32	chr21:47602432-47602482	HCM	heart:	n/a
33	chr21:47602148-47602198	BE2_C	brain:	n/a
34	chr21:47602432-47602482	NHBE	bronchial:	n/a
35	chr21:47601047-47601097	MCF10A-Er-Src	breast:	n/a
36	chr21:47602432-47602482	H1-hESC	embryonic stem cell:	embryo
37	chr21:47602432-47602482	CMK	blood:	n/a
38	chr21:47602486-47602536	SK-N-SH	brain:	n/a
39	chr21:47602702-47602752	ECC-1	luminal epithelium:	n/a
40	chr21:47602702-47602752	ProgFib	skin:	n/a
41	chr21:47602432-47602482	NB4	blood:	n/a
42	chr21:47602148-47602198	HepG2	liver:	n/a
43	chr21:47602486-47602536	HCM	heart:	n/a
44	chr21:47602486-47602536	HL-60	blood:	n/a
45	chr21:47602702-47602752	Jurkat	blood:	n/a
46	chr21:47602432-47602482	HPAEpiC	pulmonary alveolar:	n/a
47	chr21:47602148-47602198	T-47D	breast:	n/a
48	chr21:47601047-47601097	HCM	heart:	n/a
49	chr21:47601150-47601200	HRE	kidney:	n/a
50	chr21:47602432-47602482	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
2	chr21:47600278..47602930-chr21:47743867..47746831,2	K562	blood:
3	chr21:47573796..47576021-chr21:47598325..47600385,2	K562	blood:
4	chr21:47572549..47576001-chr21:47599228..47602499,3	MCF-7	breast:
5	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
6	chr21:47601827..47605045-chr21:47646095..47649627,4	MCF-7	breast:
7	chr21:47599873..47602213-chr21:47649234..47651649,2	K562	blood:
8	chr21:47601203..47604335-chr21:47632751..47634921,3	K562	blood:
9	chr21:47584368..47587107-chr21:47598667..47601448,3	MCF-7	breast:
10	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
11	chr21:47563633..47565565-chr21:47603562..47606281,2	K562	blood:
12	chr21:47575014..47577674-chr21:47594867..47597205,2	K562	blood:
13	chr21:47587472..47590076-chr21:47646984..47649833,2	MCF-7	breast:
14	chr21:47591191..47593431-chr21:47599705..47602062,3	MCF-7	breast:
15	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
16	chr21:47600262..47602297-chr21:47602464..47604765,2	K562	blood:
17	chr21:47602847..47606841-chr21:47742668..47745795,6	K562	blood:
18	chr21:47563716..47566123-chr21:47602803..47604796,2	K562	blood:
19	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
20	chr21:47588823..47590462-chr21:47601081..47603080,2	MCF-7	breast:
21	chr21:47594311..47596914-chr21:47599495..47600996,2	K562	blood:
22	chr21:47602452..47604357-chr21:47877079..47880272,3	K562	blood:
23	chr21:47571733..47573390-chr21:47601169..47604058,2	K562	blood:
24	chr21:47580435..47582947-chr21:47589052..47590591,2	K562	blood:
25	chr21:47579510..47581260-chr21:47592233..47594320,2	K562	blood:
26	chr21:47600488..47602703-chr21:47632844..47634921,2	K562	blood:
27	chr21:47598526..47600624-chr21:47604926..47607198,2	K562	blood:
28	chr21:47568990..47571521-chr21:47602008..47603891,2	K562	blood:
29	chr21:47598086..47600168-chr21:47602807..47604710,2	K562	blood:
30	chr21:47591887..47593806-chr21:47599783..47602845,3	K562	blood:
31	chr21:47602500..47604164-chr21:47614586..47616622,2	K562	blood:
32	chr21:47599317..47602217-chr21:47649153..47650672,2	K562	blood:
33	chr21:47602595..47605401-chr21:47649000..47651929,3	K562	blood:
34	chr21:47572189..47573895-chr21:47587183..47588702,2	K562	blood:
35	chr21:47603167..47605215-chr21:47743246..47745709,3	K562	blood:
36	chr21:47591492..47594026-chr21:47596355..47598597,2	K562	blood:
37	chr21:47540169..47542673-chr21:47591421..47593527,2	MCF-7	breast:

No data

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

Extended variants
information (count: 812 )
Associated
traits (count: 36 )

Variant overlapped rSNPs/rCNVs (count:812 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77889636	chr21:47588465-47588466	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs561457465	chr21:47588469-47588470	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528241329	chr21:47588481-47588482	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540248819	chr21:47588536-47588537	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs369176014	chr21:47588540-47588541	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531977796	chr21:47588561-47588562	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550872680	chr21:47588577-47588578	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs569011729	chr21:47588610-47588611	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs146820112	chr21:47588623-47588624	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs560270320	chr21:47588633-47588634	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548022105	chr21:47588636-47588637	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs566327442	chr21:47588637-47588638	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs11909543	chr21:47588646-47588647	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs139572736	chr21:47588689-47588690	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577984682	chr21:47588690-47588691	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs538630265	chr21:47588694-47588695	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs58861127	chr21:47588735-47588736	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs575885966	chr21:47588736-47588737	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs61140994	chr21:47588743-47588744	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs146604399	chr21:47588780-47588781	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs564783696	chr21:47588789-47588790	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs28588245	chr21:47588791-47588792	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs540345533	chr21:47588802-47588803	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs533422076	chr21:47588803-47588804	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532134634	chr21:47588808-47588809	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs61396606	chr21:47588834-47588835	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186693765	chr21:47588877-47588878	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs377159305	chr21:47588888-47588889	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs192416480	chr21:47588940-47588941	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs183973311	chr21:47588946-47588947	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs529983733	chr21:47589044-47589045	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs61483198	chr21:47589046-47589047	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs370806435	chr21:47589061-47589062	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs2839128	chr21:47589099-47589100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs547095031	chr21:47589114-47589115	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571605187	chr21:47589115-47589116	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs4819211	chr21:47589136-47589137	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs187603423	chr21:47589141-47589142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs141116527	chr21:47589146-47589147	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs536979376	chr21:47589153-47589154	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs9980792	chr21:47589156-47589157	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs9977340	chr21:47589168-47589169	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs540423067	chr21:47589174-47589175	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs367822514	chr21:47589176-47589177	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs199725013	chr21:47589182-47589183	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs76802500	chr21:47589184-47589185	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs28611289	chr21:47589194-47589195	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs71324496	chr21:47589198-47589199	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs75009205	chr21:47589207-47589208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs558631044	chr21:47589212-47589213	Weak transcription Strong 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:446 , 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	chr21:47581600-47588800	Weak transcription	Spleen	Spleen
16	chr21:47581600-47590000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr21:47581600-47600000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr21:47581600-47600200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr21:47582000-47592800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr21:47582000-47602200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr21:47582000-47602800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr21:47582000-47602800	Weak transcription	Ovary	ovary
23	chr21:47582200-47591600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr21:47582400-47600200	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr21:47582400-47603800	Weak transcription	Thymus	Thymus
26	chr21:47582600-47592200	Weak transcription	Fetal Intestine Small	intestine
27	chr21:47583000-47602800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr21:47583600-47588600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr21:47583600-47594000	Weak transcription	Fetal Lung	lung
30	chr21:47583800-47590800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr21:47585800-47592200	Weak transcription	K562	blood
32	chr21:47587400-47588800	Strong transcription	Fetal Stomach	stomach
33	chr21:47587400-47589000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr21:47587400-47589400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr21:47587600-47588600	Strong transcription	Fetal Muscle Leg	muscle
36	chr21:47587800-47592200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr21:47588000-47588600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr21:47588000-47588600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr21:47588000-47588800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr21:47588000-47588800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr21:47588000-47588800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr21:47588000-47589000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr21:47588000-47589000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr21:47588000-47589200	Strong transcription	Fetal Muscle Trunk	muscle
45	chr21:47588200-47588600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr21:47588400-47588600	Genic enhancers	Lung	lung
47	chr21:47588400-47589000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr21:47588600-47589000	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr21:47588600-47592000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr21:47588600-47592400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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