Variant report

Variant	esv3529214
Chromosome Location	chr21:45617222-45622747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:175)
CpG islands
(count:366)
Chromatin interactive
region (count:25)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:175 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr21:45622503-45622974	K562	blood:	n/a	n/a
2	ATF3	chr21:45622485-45622869	K562	blood:	n/a	n/a
3	BHLHE40	chr21:45622180-45622754	K562	blood:	n/a	chr21:45622610-45622626
4	BHLHE40	chr21:45617016-45617223	K562	blood:	n/a	n/a
5	CCNT2	chr21:45622415-45622989	K562	blood:	n/a	n/a
6	CEBPB	chr21:45622344-45623035	MCF-7	breast:	n/a	chr21:45622707-45622718
7	CEBPB	chr21:45622529-45622896	H1-hESC	embryonic stem cell:	n/a	chr21:45622707-45622718
8	CEBPB	chr21:45622535-45622877	HepG2	liver:	n/a	chr21:45622707-45622718
9	CEBPB	chr21:45622427-45623040	MCF-7	breast:	n/a	chr21:45622707-45622718
10	CEBPB	chr21:45622525-45622899	K562	blood:	n/a	chr21:45622707-45622718
11	CEBPB	chr21:45619441-45619519	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr21:45622544-45622829	K562	blood:	n/a	chr21:45622707-45622718
13	CEBPB	chr21:45622576-45622838	A549	lung:	n/a	chr21:45622707-45622718
14	CEBPB	chr21:45622516-45622927	Hela-S3	cervix:	n/a	chr21:45622707-45622718
15	CEBPB	chr21:45622519-45622908	IMR90	lung:	n/a	chr21:45622707-45622718
16	CEBPB	chr21:45622637-45622757	HepG2	liver:	n/a	chr21:45622707-45622718
17	CEBPB	chr21:45622518-45622870	K562	blood:	n/a	chr21:45622707-45622718
18	CHD2	chr21:45622585-45622596	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr21:45619426-45619622	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr21:45622579-45622899	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr21:45622700-45622850	HCM	heart:	n/a	n/a
22	CTCF	chr21:45622580-45622730	AG04449	skin:	n/a	n/a
23	E2F4	chr21:45622579-45622879	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr21:45622227-45623016	K562	blood:	n/a	n/a
25	E2F6	chr21:45619188-45619821	H1-hESC	embryonic stem cell:	n/a	n/a
26	E2F6	chr21:45619315-45619695	H1-hESC	embryonic stem cell:	n/a	n/a
27	EGR1	chr21:45619341-45619664	H1-hESC	embryonic stem cell:	n/a	n/a
28	ELK1	chr21:45622636-45622871	Hela-S3	cervix:	n/a	n/a
29	ELK4	chr21:45622565-45622843	Hela-S3	cervix:	n/a	n/a
30	EP300	chr21:45622366-45623075	K562	blood:	n/a	chr21:45622704-45622718
31	EP300	chr21:45619295-45619688	H1-hESC	embryonic stem cell:	n/a	n/a
32	EP300	chr21:45622493-45622984	T-47D	breast:	n/a	chr21:45622704-45622718
33	EP300	chr21:45622396-45622944	T-47D	breast:	n/a	chr21:45622704-45622718
34	FOS	chr21:45622566-45622884	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr21:45622536-45622919	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr21:45622564-45622853	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr21:45622564-45622890	MCF10A-Er-Src	breast:	n/a	n/a
38	FOXA1	chr21:45622430-45622859	T-47D	breast:	n/a	n/a
39	FOXP2	chr21:45622218-45623115	PFSK-1	brain:	n/a	n/a
40	GATA2	chr21:45621258-45621452	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr21:45621142-45621611	MCF-7	breast:	n/a	n/a
42	GATA3	chr21:45621316-45621542	MCF-7	breast:	n/a	n/a
43	GATA3	chr21:45621141-45621571	T-47D	breast:	n/a	n/a
44	GATA3	chr21:45622533-45622896	T-47D	breast:	n/a	n/a
45	GATA3	chr21:45621149-45621580	T-47D	breast:	n/a	n/a
46	GATA3	chr21:45621020-45621547	MCF-7	breast:	n/a	n/a
47	GATA3	chr21:45620986-45621619	MCF-7	breast:	n/a	n/a
48	GTF2F1	chr21:45619491-45619566	H1-hESC	embryonic stem cell:	n/a	n/a
49	GTF2F1	chr21:45622533-45622792	Hela-S3	cervix:	n/a	n/a
50	GTF2F1	chr21:45622502-45622508	H1-hESC	embryonic stem cell:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45622373-45622423	HAEpiC	amniotic membrane:	n/a
2	chr21:45622219-45622269	HCT-116	colon:	n/a
3	chr21:45622493-45622543	K562	blood:	n/a
4	chr21:45622096-45622146	NHBE	bronchial:	n/a
5	chr21:45622122-45622172	HCPEpiC	choroid plexus:	n/a
6	chr21:45622096-45622146	HRE	kidney:	n/a
7	chr21:45619449-45619499	MCF10A-Er-Src	breast:	n/a
8	chr21:45622373-45622423	HCT-116	colon:	n/a
9	chr21:45622493-45622543	A549	lung:	n/a
10	chr21:45619449-45619499	HPAEpiC	pulmonary alveolar:	n/a
11	chr21:45622493-45622543	RPTEC	kidney:	n/a
12	chr21:45622122-45622172	AoSMC	blood vessel:	n/a
13	chr21:45622122-45622172	BJ	skin:	n/a
14	chr21:45622096-45622146	NT2-D1	testis:	n/a
15	chr21:45622219-45622269	AoSMC	blood vessel:	n/a
16	chr21:45622493-45622543	AG04449	skin:	fetal
17	chr21:45622493-45622543	Hepatocyte	liver:	n/a
18	chr21:45622122-45622172	HRPEpiC	eye:	n/a
19	chr21:45622219-45622269	Caco-2	colon:	n/a
20	chr21:45622373-45622423	NT2-D1	testis:	n/a
21	chr21:45622122-45622172	Caco-2	colon:	n/a
22	chr21:45622219-45622269	NH-A	brain:	n/a
23	chr21:45622373-45622423	HMEC	breast:	n/a
24	chr21:45619449-45619499	HL-60	blood:	n/a
25	chr21:45622493-45622543	HEEpiC	esophagus:	n/a
26	chr21:45622493-45622543	Caco-2	colon:	n/a
27	chr21:45622122-45622172	SKMC	muscle:	n/a
28	chr21:45622373-45622423	NB4	blood:	n/a
29	chr21:45622219-45622269	T-47D	breast:	n/a
30	chr21:45622493-45622543	HCT-116	colon:	n/a
31	chr21:45622493-45622543	GM19239	blood:	n/a
32	chr21:45622219-45622269	GM12878	blood:	n/a
33	chr21:45622373-45622423	HPAEpiC	pulmonary alveolar:	n/a
34	chr21:45619449-45619499	PANC-1	pancreas:	n/a
35	chr21:45619449-45619499	HNPCEpiC	eye:	n/a
36	chr21:45622219-45622269	SK-N-SH	brain:	n/a
37	chr21:45622096-45622146	HCT-116	colon:	n/a
38	chr21:45622219-45622269	IMR90	lung:	fetal
39	chr21:45622122-45622172	AG04449	skin:	fetal
40	chr21:45622219-45622269	GM19239	blood:	n/a
41	chr21:45622493-45622543	MCF10A-Er-Src	breast:	n/a
42	chr21:45622373-45622423	ECC-1	luminal epithelium:	n/a
43	chr21:45622122-45622172	K562	blood:	n/a
44	chr21:45622219-45622269	HEEpiC	esophagus:	n/a
45	chr21:45622493-45622543	IMR90	lung:	fetal
46	chr21:45622122-45622172	SK-N-SH	brain:	n/a
47	chr21:45622493-45622543	U87	brain:	n/a
48	chr21:45622373-45622423	HUVEC	blood vessel:	n/a
49	chr21:45622096-45622146	HPAEpiC	pulmonary alveolar:	n/a
50	chr21:45619449-45619499	T-47D	breast:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45622485..45624278-chr21:45668242..45670471,2	MCF-7	breast:
2	chr21:45621411..45624934-chr21:45718058..45721352,4	MCF-7	breast:
3	chr21:45620857..45623394-chr21:45709649..45711804,3	MCF-7	breast:
4	chr21:45565762..45568425-chr21:45616246..45618901,2	MCF-7	breast:
5	chr21:45580625..45582180-chr21:45622469..45623971,2	MCF-7	breast:
6	chr21:45621565..45624005-chr21:45712576..45714212,3	MCF-7	breast:
7	chr21:45557116..45559735-chr21:45615528..45618206,3	MCF-7	breast:
8	chr21:45622629..45624491-chr21:45663848..45665509,2	MCF-7	breast:
9	chr21:45620341..45625358-chr21:45718389..45721509,5	MCF-7	breast:
10	chr21:45621786..45624650-chr21:45632661..45635247,3	MCF-7	breast:
11	chr21:45588739..45594310-chr21:45621185..45624296,6	MCF-7	breast:
12	chr21:45577492..45580364-chr21:45620942..45622616,2	K562	blood:
13	chr21:45552930..45554458-chr21:45622046..45624839,2	MCF-7	breast:
14	chr21:45621014..45626357-chr21:45626432..45630019,5	K562	blood:
15	chr21:45620311..45631567-chr21:45651002..45670824,52	MCF-7	breast:
16	chr21:45616221..45617876-chr21:45625272..45628231,2	K562	blood:
17	chr21:45612993..45620081-chr21:45620303..45625017,17	MCF-7	breast:
18	chr21:45568616..45570755-chr21:45615083..45617675,2	K562	blood:
19	chr21:45610715..45617377-chr21:45717031..45721978,7	MCF-7	breast:
20	chr21:45621014..45624737-chr21:45625090..45629806,7	K562	blood:
21	chr21:45619816..45631884-chr21:45656529..45663802,30	MCF-7	breast:
22	chr21:45615189..45618434-chr21:45625221..45628569,5	MCF-7	breast:
23	chr21:45567927..45569479-chr21:45614833..45617390,2	K562	blood:
24	chr21:45615502..45617869-chr21:45667459..45670293,2	K562	blood:
25	chr21:45614676..45619255-chr21:45657692..45665676,14	MCF-7	breast:

(count:6 , 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
3	lnc-C21orf33-2	chr21:45621173-45621840	XLOC_013967
4	lnc-ICOSLG-7	chr21:45622544-45622770	NONHSAT082495
5	lnc-C21orf33-2	chr21:45622449-45622579	XLOC_013967
6	lnc-ICOSLG-1	chr21:45621679-45621840	NONHSAT082494

No data

Variant related genes	Relation type
ENSG00000232124	TF binding region
ENSG00000232124	CpG island
ENSG00000267913	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000232124	chromatin interactions
ENSG00000225331	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000160224	chromatin interactions
ENSG00000232010	chromatin interactions
ENSG00000232698	chromatin interactions

Extended variants
information (count: 275 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2032325	chr21:45617242-45617243	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
2	rs117425406	chr21:45617248-45617249	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs149387235	chr21:45617252-45617253	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs2032326	chr21:45617279-45617280	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	rs535004349	chr21:45617308-45617309	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs547148576	chr21:45617313-45617314	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs144783484	chr21:45617314-45617315	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs557903423	chr21:45617321-45617322	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	rs531007999	chr21:45617417-45617418	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs551736333	chr21:45617418-45617419	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs11909529	chr21:45617430-45617431	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs561548056	chr21:45617436-45617437	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs528521105	chr21:45617442-45617443	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs77291583	chr21:45617497-45617498	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs546985275	chr21:45617500-45617501	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs146645229	chr21:45617504-45617505	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs202167793	chr21:45617580-45617581	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs111463136	chr21:45617581-45617582	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	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
30	rs77325606	chr21:45617694-45617695	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs569881838	chr21:45617710-45617711	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs536844956	chr21:45617747-45617748	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs376029949	chr21:45617761-45617762	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs567201818	chr21:45617810-45617811	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs534339006	chr21:45617821-45617822	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs552511356	chr21:45617824-45617825	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs577667217	chr21:45617839-45617840	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs377583244	chr21:45617851-45617852	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs181654805	chr21:45617874-45617875	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs8129605	chr21:45617878-45617879	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs35120546	chr21:45617960-45617961	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs575826992	chr21:45617963-45617964	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs77117524	chr21:45617965-45617966	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs77982069	chr21:45617974-45617975	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs397867427	chr21:45617975-45617976	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs76791047	chr21:45617976-45617977	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs543220413	chr21:45617980-45617981	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs561587770	chr21:45617981-45617982	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs376795144	chr21:45617988-45617989	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs59380543	chr21:45617996-45617997	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	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:176 , 50 per page) page: 1 2 3 4

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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