Variant report

Variant	nsv588936
Chromosome Location	chr22:34106745-34226592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:677)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:88)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:34219541-34219836	HepG2	liver:	n/a	n/a
2	ATF2	chr22:34185841-34186312	GM12878	blood:	n/a	n/a
3	ATF2	chr22:34183459-34184387	GM12878	blood:	n/a	n/a
4	ATF2	chr22:34183601-34184137	GM12878	blood:	n/a	n/a
5	ATF2	chr22:34181226-34181686	GM12878	blood:	n/a	n/a
6	ATF2	chr22:34185755-34186363	GM12878	blood:	n/a	n/a
7	BACH1	chr22:34225564-34225840	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr22:34221773-34221807	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr22:34135101-34135251	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr22:34183589-34183875	GM12878	blood:	n/a	n/a
11	BATF	chr22:34185838-34186311	GM12878	blood:	n/a	n/a
12	BATF	chr22:34154766-34154993	GM12878	blood:	n/a	n/a
13	BATF	chr22:34184057-34184349	GM12878	blood:	n/a	n/a
14	BATF	chr22:34185847-34186124	GM12878	blood:	n/a	n/a
15	BCL11A	chr22:34183569-34183918	GM12878	blood:	n/a	n/a
16	BCL3	chr22:34153825-34154068	GM12878	blood:	n/a	n/a
17	BCL3	chr22:34185878-34186387	GM12878	blood:	n/a	n/a
18	BCL3	chr22:34139772-34140140	GM12878	blood:	n/a	n/a
19	BCLAF1	chr22:34181218-34181676	GM12878	blood:	n/a	n/a
20	BCLAF1	chr22:34185839-34186424	GM12878	blood:	n/a	n/a
21	BCLAF1	chr22:34183601-34183918	GM12878	blood:	n/a	n/a
22	BCLAF1	chr22:34183553-34184056	GM12878	blood:	n/a	n/a
23	BHLHE40	chr22:34185856-34186187	GM12878	blood:	n/a	n/a
24	BHLHE40	chr22:34119934-34120194	GM12878	blood:	n/a	n/a
25	BHLHE40	chr22:34114028-34114321	HepG2	liver:	n/a	n/a
26	BHLHE40	chr22:34168931-34169192	GM12878	blood:	n/a	n/a
27	BHLHE40	chr22:34202110-34202534	GM12878	blood:	n/a	n/a
28	CEBPB	chr22:34217100-34217196	HepG2	liver:	n/a	chr22:34217123-34217134
29	CEBPB	chr22:34181187-34181655	IMR90	lung:	n/a	n/a
30	CEBPB	chr22:34160080-34160369	IMR90	lung:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
31	CEBPB	chr22:34142582-34142926	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
32	CEBPB	chr22:34160056-34160345	A549	lung:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
33	CEBPB	chr22:34142598-34142923	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
34	CEBPB	chr22:34194364-34194659	HepG2	liver:	n/a	chr22:34194414-34194427
35	CEBPB	chr22:34177308-34177537	IMR90	lung:	n/a	n/a
36	CEBPB	chr22:34142642-34142976	A549	lung:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
37	CEBPB	chr22:34160038-34160378	HepG2	liver:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
38	CEBPB	chr22:34153833-34154197	HepG2	liver:	n/a	n/a
39	CEBPB	chr22:34160073-34160312	H1-hESC	embryonic stem cell:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
40	CEBPB	chr22:34142695-34142833	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
41	CHD1	chr22:34218027-34218094	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr22:34165725-34165749	GM12878	blood:	n/a	n/a
43	CTCF	chr22:34215840-34215990	GM12878	blood:	n/a	n/a
44	CTCF	chr22:34152511-34152676	GM19240	blood:	n/a	n/a
45	CTCF	chr22:34215820-34216021	HepG2	liver:	n/a	n/a
46	CTCF	chr22:34215849-34216042	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr22:34152508-34152707	GM12892	blood:	n/a	n/a
48	CTCF	chr22:34152556-34152642	GM13977	blood:	n/a	n/a
49	CTCF	chr22:34152480-34152630	GM12878	blood:	n/a	n/a
50	CTCF	chr22:34181152-34181188	GM10248	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34192387-34192437	MCF-7	breast:	n/a
2	chr22:34192387-34192437	MCF10A-Er-Src	breast:	n/a
3	chr22:34192387-34192437	HUVEC	blood vessel:	n/a
4	chr22:34192387-34192437	SK-N-SH	brain:	n/a
5	chr22:34192387-34192437	HNPCEpiC	eye:	n/a
6	chr22:34192387-34192437	H1-hESC	embryonic stem cell:	embryo
7	chr22:34192387-34192437	HCPEpiC	choroid plexus:	n/a
8	chr22:34192387-34192437	AG10803	skin:	n/a
9	chr22:34192387-34192437	AG04449	skin:	fetal
10	chr22:34192387-34192437	HPAEpiC	pulmonary alveolar:	n/a
11	chr22:34192387-34192437	ProgFib	skin:	n/a
12	chr22:34192387-34192437	SK-N-SH_RA	brain:	n/a
13	chr22:34192387-34192437	GM12892	blood:	n/a
14	chr22:34192387-34192437	PFSK-1	brain:	n/a
15	chr22:34192387-34192437	AoSMC	blood vessel:	n/a
16	chr22:34192387-34192437	BJ	skin:	n/a
17	chr22:34192387-34192437	HRPEpiC	eye:	n/a
18	chr22:34192387-34192437	T-47D	breast:	n/a
19	chr22:34192387-34192437	GM12891	blood:	n/a
20	chr22:34192387-34192437	HCM	heart:	n/a
21	chr22:34192387-34192437	GM19239	blood:	n/a
22	chr22:34192387-34192437	HEK293	kidney:	embryo
23	chr22:34192387-34192437	NH-A	brain:	n/a
24	chr22:34192387-34192437	AG04450	lung:	fetal
25	chr22:34192387-34192437	GM06990	blood:	n/a
26	chr22:34192387-34192437	HRE	kidney:	n/a
27	chr22:34192387-34192437	HMEC	breast:	n/a
28	chr22:34192387-34192437	HEEpiC	esophagus:	n/a
29	chr22:34192387-34192437	SAEC	small airway:	n/a
30	chr22:34192387-34192437	HepG2	liver:	n/a
31	chr22:34192387-34192437	HCT-116	colon:	n/a
32	chr22:34192387-34192437	CMK	blood:	n/a
33	chr22:34192387-34192437	IMR90	lung:	fetal
34	chr22:34192387-34192437	BE2_C	brain:	n/a
35	chr22:34192387-34192437	A549	lung:	n/a
36	chr22:34192387-34192437	AG09309	skin:	n/a
37	chr22:34192387-34192437	HL-60	blood:	n/a
38	chr22:34192387-34192437	SKMC	muscle:	n/a
39	chr22:34192387-34192437	Caco-2	colon:	n/a
40	chr22:34192387-34192437	ovcar-3	ovarian:	n/a
41	chr22:34192387-34192437	HRCEpiC	kidney:	n/a
42	chr22:34192387-34192437	AG09319	gingival:	n/a
43	chr22:34192387-34192437	NHBE	bronchial:	n/a
44	chr22:34192387-34192437	RPTEC	kidney:	n/a
45	chr22:34192387-34192437	NHDF-neo	bronchial:	n/a
46	chr22:34192387-34192437	NT2-D1	testis:	n/a
47	chr22:34192387-34192437	HIPEpiC	eye:	n/a
48	chr22:34192387-34192437	PrEC	prostate:	n/a
49	chr22:34192387-34192437	HCF	heart:	n/a
50	chr22:34192387-34192437	Jurkat	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:34143232..34145432-chr22:34315745..34318657,2	MCF-7	breast:
2	chr22:34181411..34183196-chr22:34314966..34317332,2	MCF-7	breast:
3	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
4	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
5	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
6	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
7	chr22:34172664..34173221-chr22:34313368..34314036,2	MCF-7	breast:
8	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
9	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
10	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:
11	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:

(count:88 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
2	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085013
3	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085015
4	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085015
5	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
6	lnc-TIMP3-6	chr22:34139996-34140315	ENSG00000224973.1
7	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085014
8	lnc-TIMP3-6	chr22:34146591-34146803	NONHSAT085011
9	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
10	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
11	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085013
12	lnc-TIMP3-6	chr22:34140116-34140179	ENSG00000224973.1
13	lnc-TIMP3-6	chr22:34133550-34133769	ENSG00000224973.1
14	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085012
15	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085011
16	lnc-SYN3-4	chr22:34119818-34120265	ENSG00000232081.1
17	lnc-TIMP3-6	chr22:34146591-34146644	ENSG00000224973.1
18	lnc-TIMP3-6	chr22:34120972-34121087	NONHSAT085011
19	lnc-TIMP3-6	chr22:34121000-34121087	NONHSAT085013
20	lnc-TIMP3-6	chr22:34128242-34129671	ENSG00000224973.1
21	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085014
22	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
23	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085014
24	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1
25	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085018
26	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
27	lnc-TIMP3-6	chr22:34133550-34133769	ENSG00000224973.1
28	lnc-TIMP3-6	chr22:34121003-34121087	NONHSAT085014
29	lnc-TIMP3-6	chr22:34146591-34146729	ENSG00000224973.1
30	lnc-TIMP3-6	chr22:34123477-34123574	NONHSAT085013
31	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085014
32	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085015
33	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
34	lnc-TIMP3-6	chr22:34146591-34146830	ENSG00000224973.1
35	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085011
36	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085014
37	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085018
38	lnc-TIMP3-6	chr22:34120972-34121087	NONHSAT085012
39	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085015
40	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085011
41	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085015
42	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085012
43	lnc-TIMP3-6	chr22:34133550-34133769	ENSG00000224973.1
44	lnc-TIMP3-6	chr22:34121000-34121087	ENSG00000224973.1
45	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085018
46	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085011
47	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085012
48	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085014
49	lnc-TIMP3-6	chr22:34121055-34121087	ENSG00000224973.1
50	lnc-TIMP3-6	chr22:34121026-34121087	ENSG00000224973.1

No data

Variant related genes	Relation type
LARGE-AS1	TF binding region
LARGE-IT1	TF binding region
LARGE-AS1	CpG island
LARGE-IT1	CpG island
ENSG00000133424	chromatin interactions
ENSG00000273082	chromatin interactions

Extended variants
information (count: 5333 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:5333 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6518838	chr22:34106745-34106746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553137195	chr22:34106749-34106750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566170817	chr22:34106750-34106751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73170537	chr22:34106751-34106752	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs558008331	chr22:34106755-34106756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183615252	chr22:34106756-34106757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368807001	chr22:34106767-34106768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575355209	chr22:34106782-34106783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150651793	chr22:34106793-34106794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs5999067	chr22:34106827-34106828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs2267268	chr22:34106853-34106854	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs139761195	chr22:34106867-34106868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188706328	chr22:34106869-34106870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116235265	chr22:34106872-34106873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542741766	chr22:34106954-34106955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562639642	chr22:34106970-34106971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531638589	chr22:34107014-34107015	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551373134	chr22:34107015-34107016	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192813843	chr22:34107038-34107039	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184072459	chr22:34107059-34107060	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557334961	chr22:34107063-34107064	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567567952	chr22:34107095-34107096	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9609858	chr22:34107137-34107138	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573554101	chr22:34107152-34107153	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs62225398	chr22:34107220-34107221	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs240091	chr22:34107247-34107248	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376703463	chr22:34107250-34107251	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535639754	chr22:34107252-34107253	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539169125	chr22:34107253-34107254	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111287093	chr22:34107277-34107278	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537892535	chr22:34107314-34107315	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566366133	chr22:34107363-34107364	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528205066	chr22:34107364-34107365	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535459900	chr22:34107365-34107366	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117760161	chr22:34107392-34107393	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577529787	chr22:34107404-34107405	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371738020	chr22:34107413-34107414	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534544729	chr22:34107462-34107463	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144797754	chr22:34107463-34107464	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574222795	chr22:34107488-34107489	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs240092	chr22:34107489-34107490	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373410300	chr22:34107498-34107499	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186885596	chr22:34107516-34107517	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576134849	chr22:34107523-34107524	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545073064	chr22:34107581-34107582	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73402821	chr22:34107600-34107601	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs377418890	chr22:34107602-34107603	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527661296	chr22:34107611-34107612	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536633773	chr22:34107630-34107631	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546918041	chr22:34107637-34107638	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1859 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34087000-34109400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr22:34091600-34115800	Weak transcription	Pancreas	Pancrea
3	chr22:34092400-34109200	Weak transcription	Fetal Intestine Large	intestine
4	chr22:34097000-34110000	Weak transcription	Ovary	ovary
5	chr22:34097200-34108000	Weak transcription	Fetal Intestine Small	intestine
6	chr22:34097200-34109200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr22:34097200-34109200	Weak transcription	Fetal Brain Female	brain
8	chr22:34097200-34109400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr22:34097400-34107400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr22:34097600-34110200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr22:34097600-34114600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr22:34098200-34110600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr22:34100400-34109000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr22:34100600-34108200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr22:34100800-34110000	Weak transcription	Primary B cells from peripheral blood	blood
16	chr22:34101200-34108800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr22:34101200-34109600	Weak transcription	Fetal Stomach	stomach
18	chr22:34101200-34110000	Weak transcription	Aorta	Aorta
19	chr22:34103200-34110600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr22:34104000-34107400	Weak transcription	Stomach Mucosa	stomach
21	chr22:34104000-34110000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr22:34104200-34118800	Weak transcription	Right Ventricle	heart
23	chr22:34104600-34109400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr22:34105000-34109800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr22:34105200-34109800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr22:34105600-34133400	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr22:34105800-34107400	Enhancers	HSMMtube	muscle
28	chr22:34106000-34107200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr22:34106000-34107200	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr22:34106000-34107200	Enhancers	HSMM	muscle
31	chr22:34106200-34107200	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr22:34106200-34107400	Weak transcription	Fetal Heart	heart
33	chr22:34106400-34106800	Enhancers	Brain Anterior Caudate	brain
34	chr22:34106400-34107200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr22:34106400-34107200	Enhancers	Brain Angular Gyrus	brain
36	chr22:34106400-34107200	Enhancers	Psoas Muscle	Psoas
37	chr22:34106400-34110200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr22:34106600-34106800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr22:34106600-34107000	Weak transcription	Left Ventricle	heart
40	chr22:34106600-34109200	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr22:34106600-34109400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr22:34106600-34109400	Weak transcription	Brain Cingulate Gyrus	brain
43	chr22:34106600-34109400	Weak transcription	Brain Hippocampus Middle	brain
44	chr22:34106600-34110000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr22:34106800-34108400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr22:34107000-34107600	Genic enhancers	Left Ventricle	heart
47	chr22:34107200-34109800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr22:34107200-34110000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr22:34107200-34110000	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr22:34107400-34107600	Enhancers	Stomach Mucosa	stomach

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