Variant report

Variant	nsv587723
Chromosome Location	chr21:45617328-45620705
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr21:45619441-45619519	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr21:45619426-45619622	H1-hESC	embryonic stem cell:	n/a	n/a
3	E2F6	chr21:45619188-45619821	H1-hESC	embryonic stem cell:	n/a	n/a
4	E2F6	chr21:45619315-45619695	H1-hESC	embryonic stem cell:	n/a	n/a
5	EGR1	chr21:45619341-45619664	H1-hESC	embryonic stem cell:	n/a	n/a
6	EP300	chr21:45619295-45619688	H1-hESC	embryonic stem cell:	n/a	n/a
7	GTF2F1	chr21:45619491-45619566	H1-hESC	embryonic stem cell:	n/a	n/a
8	HMGN3	chr21:45617133-45617338	K562	blood:	n/a	n/a
9	JUN	chr21:45615817-45617579	K562	blood:	n/a	n/a
10	JUN	chr21:45619451-45619644	H1-hESC	embryonic stem cell:	n/a	n/a
11	JUND	chr21:45619595-45619702	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr21:45619242-45619829	H1-hESC	embryonic stem cell:	n/a	n/a
13	MAX	chr21:45619437-45619539	GM12878	blood:	n/a	n/a
14	MAX	chr21:45616966-45617344	K562	blood:	n/a	n/a
15	MAX	chr21:45619325-45619719	H1-hESC	embryonic stem cell:	n/a	n/a
16	MAX	chr21:45619288-45619712	H1-hESC	embryonic stem cell:	n/a	n/a
17	MXI1	chr21:45619322-45619628	H1-hESC	embryonic stem cell:	n/a	n/a
18	MXI1	chr21:45619461-45619560	GM12878	blood:	n/a	n/a
19	MYC	chr21:45619375-45619651	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr21:45615517-45617531	GM12878	blood:	n/a	n/a
21	POLR2A	chr21:45615624-45617413	HL-60	blood:	n/a	n/a
22	POU2F2	chr21:45619409-45619587	GM12878	blood:	n/a	chr21:45619515-45619528
23	POU2F2	chr21:45619328-45619707	GM12878	blood:	n/a	chr21:45619515-45619528
24	POU2F2	chr21:45619275-45619788	GM12878	blood:	n/a	chr21:45619515-45619528
25	POU2F2	chr21:45619288-45619698	GM12891	blood:	n/a	chr21:45619515-45619528
26	POU2F2	chr21:45619297-45619644	GM12891	blood:	n/a	chr21:45619515-45619528
27	RUNX3	chr21:45620662-45621038	GM12878	blood:	n/a	n/a
28	SIN3A	chr21:45619321-45619614	H1-hESC	embryonic stem cell:	n/a	n/a
29	SP1	chr21:45619376-45619673	H1-hESC	embryonic stem cell:	n/a	chr21:45619540-45619551
30	SP1	chr21:45619347-45619667	H1-hESC	embryonic stem cell:	n/a	chr21:45619540-45619551
31	TCF12	chr21:45619317-45619610	GM12878	blood:	n/a	n/a
32	TCF12	chr21:45619289-45619548	H1-hESC	embryonic stem cell:	n/a	n/a
33	TCF3	chr21:45619400-45619543	GM12878	blood:	n/a	n/a
34	TEAD4	chr21:45619405-45619777	H1-hESC	embryonic stem cell:	n/a	n/a
35	UBTF	chr21:45617003-45617368	K562	blood:	n/a	n/a
36	USF1	chr21:45619313-45619581	H1-hESC	embryonic stem cell:	n/a	n/a
37	USF1	chr21:45619311-45619581	H1-hESC	embryonic stem cell:	n/a	n/a
38	USF2	chr21:45619460-45619607	H1-hESC	embryonic stem cell:	n/a	n/a
39	YY1	chr21:45619323-45619681	GM12878	blood:	n/a	n/a
40	YY1	chr21:45619219-45619752	H1-hESC	embryonic stem cell:	n/a	n/a
41	YY1	chr21:45619304-45619576	GM12892	blood:	n/a	n/a
42	YY1	chr21:45619385-45619528	K562	blood:	n/a	n/a
43	YY1	chr21:45619306-45619614	GM12878	blood:	n/a	n/a
44	YY1	chr21:45619307-45619695	H1-hESC	embryonic stem cell:	n/a	n/a
45	YY1	chr21:45619340-45619542	GM12891	blood:	n/a	n/a
46	ZEB1	chr21:45619282-45619528	GM12878	blood:	n/a	n/a
47	ZNF263	chr21:45617633-45617805	HEK293-T-REx	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45619449-45619499	AoSMC	blood vessel:	n/a
2	chr21:45619449-45619499	HIPEpiC	eye:	n/a
3	chr21:45619449-45619499	HEK293	kidney:	embryo
4	chr21:45619449-45619499	Caco-2	colon:	n/a
5	chr21:45619449-45619499	BJ	skin:	n/a
6	chr21:45619449-45619499	GM12892	blood:	n/a
7	chr21:45619449-45619499	HRCEpiC	kidney:	n/a
8	chr21:45619449-45619499	GM19239	blood:	n/a
9	chr21:45619449-45619499	H1-hESC	embryonic stem cell:	embryo
10	chr21:45619449-45619499	SK-N-SH_RA	brain:	n/a
11	chr21:45619449-45619499	HAEpiC	amniotic membrane:	n/a
12	chr21:45619449-45619499	HL-60	blood:	n/a
13	chr21:45619449-45619499	SK-N-MC	brain:	n/a
14	chr21:45619449-45619499	U87	brain:	n/a
15	chr21:45619449-45619499	AG10803	skin:	n/a
16	chr21:45619449-45619499	T-47D	breast:	n/a
17	chr21:45619449-45619499	HCM	heart:	n/a
18	chr21:45619449-45619499	NHDF-neo	bronchial:	n/a
19	chr21:45619449-45619499	SKMC	muscle:	n/a
20	chr21:45619449-45619499	CMK	blood:	n/a
21	chr21:45619449-45619499	Hela-S3	cervix:	n/a
22	chr21:45619449-45619499	Jurkat	blood:	n/a
23	chr21:45619449-45619499	HRPEpiC	eye:	n/a
24	chr21:45619449-45619499	NH-A	brain:	n/a
25	chr21:45619449-45619499	AG09309	skin:	n/a
26	chr21:45619449-45619499	Hepatocyte	liver:	n/a
27	chr21:45619449-45619499	MCF10A-Er-Src	breast:	n/a
28	chr21:45619449-45619499	K562	blood:	n/a
29	chr21:45619449-45619499	HCT-116	colon:	n/a
30	chr21:45619449-45619499	GM06990	blood:	n/a
31	chr21:45619449-45619499	ECC-1	luminal epithelium:	n/a
32	chr21:45619449-45619499	A549	lung:	n/a
33	chr21:45619449-45619499	GM12878	blood:	n/a
34	chr21:45619449-45619499	BE2_C	brain:	n/a
35	chr21:45619449-45619499	HRE	kidney:	n/a
36	chr21:45619449-45619499	PANC-1	pancreas:	n/a
37	chr21:45619449-45619499	PrEC	prostate:	n/a
38	chr21:45619449-45619499	HNPCEpiC	eye:	n/a
39	chr21:45619449-45619499	HPAEpiC	pulmonary alveolar:	n/a
40	chr21:45619449-45619499	MCF-7	breast:	n/a
41	chr21:45619449-45619499	PFSK-1	brain:	n/a
42	chr21:45619449-45619499	AG09319	gingival:	n/a
43	chr21:45619449-45619499	ovcar-3	ovarian:	n/a
44	chr21:45619449-45619499	SK-N-SH	brain:	n/a
45	chr21:45619449-45619499	HUVEC	blood vessel:	n/a
46	chr21:45619449-45619499	SAEC	small airway:	n/a
47	chr21:45619449-45619499	HCF	heart:	n/a
48	chr21:45619449-45619499	NB4	blood:	n/a
49	chr21:45619449-45619499	AG04449	skin:	fetal
50	chr21:45619449-45619499	HepG2	liver:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45557116..45559735-chr21:45615528..45618206,3	MCF-7	breast:
2	chr21:45567927..45569479-chr21:45614833..45617390,2	K562	blood:
3	chr21:45620341..45625358-chr21:45718389..45721509,5	MCF-7	breast:
4	chr21:45620311..45631567-chr21:45651002..45670824,52	MCF-7	breast:
5	chr21:45565762..45568425-chr21:45616246..45618901,2	MCF-7	breast:
6	chr21:45568616..45570755-chr21:45615083..45617675,2	K562	blood:
7	chr21:45615502..45617869-chr21:45667459..45670293,2	K562	blood:
8	chr21:45612993..45620081-chr21:45620303..45625017,17	MCF-7	breast:
9	chr21:45616221..45617876-chr21:45625272..45628231,2	K562	blood:
10	chr21:45619816..45631884-chr21:45656529..45663802,30	MCF-7	breast:
11	chr21:45614676..45619255-chr21:45657692..45665676,14	MCF-7	breast:
12	chr21:45615189..45618434-chr21:45625221..45628569,5	MCF-7	breast:
13	chr21:45610715..45617377-chr21:45717031..45721978,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ICOSLG-2	chr21:45620693-45621216	XLOC_014114
2	lnc-ICOSLG-2	chr21:45619132-45620582	XLOC_014114

No data

Variant related genes	Relation type
ENSG00000232124	TF binding region
ENSG00000232124	CpG island
ENSG00000232124	chromatin interactions
ENSG00000232010	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000232698	chromatin interactions
ENSG00000141959	chromatin interactions

Extended variants
information (count: 161 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:161 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2032327	chr21:45617328-45617329	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370203143	chr21:45617343-45617344	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs537305910	chr21:45617344-45617345	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs73381309	chr21:45617352-45617353	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs573343817	chr21:45617354-45617355	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs115099560	chr21:45617372-45617373	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs148140486	chr21:45617374-45617375	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs577291369	chr21:45617380-45617381	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs545280549	chr21:45617388-45617389	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs368966321	chr21:45617392-45617393	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs531007999	chr21:45617417-45617418	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs551736333	chr21:45617418-45617419	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs11909529	chr21:45617430-45617431	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs561548056	chr21:45617436-45617437	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs528521105	chr21:45617442-45617443	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs77291583	chr21:45617497-45617498	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs546985275	chr21:45617500-45617501	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs146645229	chr21:45617504-45617505	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs202167793	chr21:45617580-45617581	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs111463136	chr21:45617581-45617582	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs2032328	chr21:45617652-45617653	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs77325606	chr21:45617694-45617695	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs569881838	chr21:45617710-45617711	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs536844956	chr21:45617747-45617748	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs376029949	chr21:45617761-45617762	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs567201818	chr21:45617810-45617811	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534339006	chr21:45617821-45617822	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs552511356	chr21:45617824-45617825	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs577667217	chr21:45617839-45617840	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs377583244	chr21:45617851-45617852	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs181654805	chr21:45617874-45617875	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs8129605	chr21:45617878-45617879	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs35120546	chr21:45617960-45617961	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs575826992	chr21:45617963-45617964	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs77117524	chr21:45617965-45617966	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs77982069	chr21:45617974-45617975	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs397867427	chr21:45617975-45617976	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs76791047	chr21:45617976-45617977	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs543220413	chr21:45617980-45617981	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs561587770	chr21:45617981-45617982	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376795144	chr21:45617988-45617989	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs59380543	chr21:45617996-45617997	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs55973512	chr21:45618008-45618009	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs565235896	chr21:45618026-45618027	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs71322551	chr21:45618046-45618047	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs71322552	chr21:45618072-45618073	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs532400637	chr21:45618079-45618080	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs78716228	chr21:45618095-45618096	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs76729174	chr21:45618103-45618104	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs386819110	chr21:45618114-45618115	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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 lymphoblastic leukemia	20435627	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
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	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
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	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 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
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD
Breast cancer	21364760	CNVD
Down syndrome	21154855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45610800-45617600	Enhancers	Placenta	Placenta
2	chr21:45612800-45617400	Enhancers	Primary hematopoietic stem cells	blood
3	chr21:45613600-45617400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr21:45613600-45617400	Enhancers	Primary B cells from peripheral blood	blood
5	chr21:45614000-45617600	Enhancers	Primary B cells from cord blood	blood
6	chr21:45614400-45617400	Weak transcription	Brain Angular Gyrus	brain
7	chr21:45614800-45622400	Weak transcription	Pancreas	Pancrea
8	chr21:45615000-45623200	Weak transcription	Brain Hippocampus Middle	brain
9	chr21:45615400-45622200	Weak transcription	Fetal Lung	lung
10	chr21:45615600-45617400	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr21:45615600-45617800	Enhancers	Fetal Thymus	thymus
12	chr21:45615800-45617400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr21:45615800-45617400	Enhancers	Brain Substantia Nigra	brain
14	chr21:45615800-45617600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr21:45615800-45617800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr21:45616000-45617600	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr21:45616000-45618000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr21:45616000-45618000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr21:45616200-45617600	Bivalent Enhancer	Adipose Nuclei	Adipose
20	chr21:45616400-45617400	Enhancers	Right Atrium	heart
21	chr21:45616600-45617400	Enhancers	Primary T cells fromperipheralblood	blood
22	chr21:45616600-45617400	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr21:45616600-45617600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr21:45616600-45619400	Weak transcription	Stomach Mucosa	stomach
25	chr21:45616600-45622000	Weak transcription	Lung	lung
26	chr21:45616600-45622200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr21:45616600-45622200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr21:45616800-45617400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr21:45616800-45617400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
30	chr21:45616800-45617600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr21:45616800-45617600	Enhancers	K562	blood
32	chr21:45616800-45621600	Weak transcription	Esophagus	oesophagus
33	chr21:45616800-45622000	Weak transcription	Left Ventricle	heart
34	chr21:45616800-45622200	Weak transcription	Fetal Intestine Small	intestine
35	chr21:45616800-45622200	Weak transcription	Spleen	Spleen
36	chr21:45616800-45626600	Weak transcription	Thymus	Thymus
37	chr21:45617000-45617400	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
38	chr21:45617000-45617600	Enhancers	Right Ventricle	heart
39	chr21:45617000-45622400	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr21:45617000-45626000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr21:45617200-45617400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr21:45617200-45617600	Enhancers	Colonic Mucosa	Colon
43	chr21:45617200-45617800	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr21:45617200-45618000	Bivalent Enhancer	Fetal Stomach	stomach
45	chr21:45617200-45619400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr21:45617200-45622200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr21:45617200-45622600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr21:45617200-45623200	Weak transcription	GM12878-XiMat	blood
49	chr21:45617200-45624000	Weak transcription	Gastric	stomach
50	chr21:45617200-45626200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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