Variant report

Variant	esv3334530
Chromosome Location	chr22:31889221-31909085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:714)
CpG islands
(count:917)
Chromatin interactive
region (count:22)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:31891935-31892132	K562	blood:	n/a	n/a
2	ATF2	chr22:31892058-31892446	GM12878	blood:	n/a	n/a
3	ATF2	chr22:31891884-31892640	GM12878	blood:	n/a	n/a
4	ATF2	chr22:31890028-31890425	GM12878	blood:	n/a	n/a
5	BACH1	chr22:31891900-31893464	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr22:31891840-31892521	K562	blood:	n/a	n/a
7	BATF	chr22:31893442-31893799	GM12878	blood:	n/a	n/a
8	BCL11A	chr22:31890124-31890662	GM12878	blood:	n/a	n/a
9	BCL3	chr22:31891880-31892610	GM12878	blood:	n/a	chr22:31892187-31892200 chr22:31892122-31892131 chr22:31892191-31892204
10	BCL3	chr22:31890097-31890610	GM12878	blood:	n/a	n/a
11	BCLAF1	chr22:31891845-31893600	GM12878	blood:	n/a	chr22:31892187-31892200 chr22:31892122-31892131 chr22:31892191-31892204 chr22:31893047-31893060
12	BCLAF1	chr22:31891896-31892711	GM12878	blood:	n/a	chr22:31892187-31892200 chr22:31892122-31892131 chr22:31892191-31892204
13	BCLAF1	chr22:31889901-31890655	GM12878	blood:	n/a	n/a
14	BHLHE40	chr22:31891655-31892707	K562	blood:	n/a	n/a
15	BHLHE40	chr22:31889379-31889813	GM12878	blood:	n/a	n/a
16	BHLHE40	chr22:31890025-31890627	GM12878	blood:	n/a	n/a
17	BHLHE40	chr22:31891722-31892771	GM12878	blood:	n/a	n/a
18	BRCA1	chr22:31892309-31892657	HepG2	liver:	n/a	n/a
19	BRCA1	chr22:31891700-31891929	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr22:31892316-31892897	GM12878	blood:	n/a	n/a
21	BRCA1	chr22:31892275-31892601	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr22:31892329-31892734	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr22:31892187-31892606	K562	blood:	n/a	n/a
24	CCNT2	chr22:31892126-31892695	K562	blood:	n/a	n/a
25	CEBPB	chr22:31900440-31900533	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr22:31900299-31900814	IMR90	lung:	n/a	n/a
27	CEBPB	chr22:31890083-31890693	GM12878	blood:	n/a	n/a
28	CEBPB	chr22:31891827-31892782	GM12878	blood:	n/a	n/a
29	CEBPB	chr22:31891893-31892179	K562	blood:	n/a	n/a
30	CEBPB	chr22:31892031-31892569	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr22:31891991-31892040	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr22:31891718-31893077	GM12878	blood:	n/a	n/a
33	CHD1	chr22:31891777-31892041	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr22:31892127-31892977	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr22:31891953-31892996	GM12878	blood:	n/a	n/a
36	CHD2	chr22:31892080-31892712	K562	blood:	n/a	n/a
37	CHD2	chr22:31890160-31890229	GM12878	blood:	n/a	n/a
38	CHD2	chr22:31891989-31892851	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr22:31892292-31892761	HepG2	liver:	n/a	n/a
40	CREB1	chr22:31893219-31894054	GM12878	blood:	n/a	n/a
41	CREB1	chr22:31893409-31893973	GM12878	blood:	n/a	n/a
42	CREB1	chr22:31892240-31892600	A549	lung:	n/a	n/a
43	CTBP2	chr22:31892002-31893041	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr22:31892680-31892830	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr22:31892286-31892481	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr22:31892200-31892350	HVMF	connective:	n/a	n/a
47	CTCF	chr22:31892180-31892330	NHLF	lung:	n/a	n/a
48	CTCF	chr22:31892300-31892450	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr22:31892155-31892534	GM19238	blood:	n/a	n/a
50	CTCF	chr22:31892295-31892448	SK-N-SH_RA	brain:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:31892793-31892843	NHDF-neo	bronchial:	n/a
2	chr22:31892114-31892164	AoSMC	blood vessel:	n/a
3	chr22:31892793-31892843	NHDF-neo	bronchial:	n/a
4	chr22:31892114-31892164	AoSMC	blood vessel:	n/a
5	chr22:31892074-31892124	Jurkat	blood:	n/a
6	chr22:31893096-31893146	U87	brain:	n/a
7	chr22:31892148-31892198	ProgFib	skin:	n/a
8	chr22:31892562-31892612	AG04449	skin:	fetal
9	chr22:31891804-31891854	Hepatocyte	liver:	n/a
10	chr22:31892152-31892202	HCF	heart:	n/a
11	chr22:31891804-31891854	IMR90	lung:	fetal
12	chr22:31892114-31892164	HepG2	liver:	n/a
13	chr22:31892148-31892198	PrEC	prostate:	n/a
14	chr22:31893238-31893288	SKMC	muscle:	n/a
15	chr22:31892053-31892103	SK-N-MC	brain:	n/a
16	chr22:31892074-31892124	PANC-1	pancreas:	n/a
17	chr22:31892148-31892198	CMK	blood:	n/a
18	chr22:31892074-31892124	HAEpiC	amniotic membrane:	n/a
19	chr22:31892562-31892612	HEEpiC	esophagus:	n/a
20	chr22:31893096-31893146	A549	lung:	n/a
21	chr22:31892148-31892198	SAEC	small airway:	n/a
22	chr22:31892045-31892095	SK-N-SH	brain:	n/a
23	chr22:31892148-31892198	NHDF-neo	bronchial:	n/a
24	chr22:31889592-31889642	Caco-2	colon:	n/a
25	chr22:31893238-31893288	LNCaP	prostate:	n/a
26	chr22:31889592-31889642	PrEC	prostate:	n/a
27	chr22:31892114-31892164	PrEC	prostate:	n/a
28	chr22:31889592-31889642	GM19239	blood:	n/a
29	chr22:31892343-31892393	MCF10A-Er-Src	breast:	n/a
30	chr22:31891804-31891854	HCT-116	colon:	n/a
31	chr22:31892562-31892612	SKMC	muscle:	n/a
32	chr22:31892793-31892843	ovcar-3	ovarian:	n/a
33	chr22:31892343-31892393	AG10803	skin:	n/a
34	chr22:31892152-31892202	BE2_C	brain:	n/a
35	chr22:31892045-31892095	NT2-D1	testis:	n/a
36	chr22:31892045-31892095	AG04450	lung:	fetal
37	chr22:31893238-31893288	U87	brain:	n/a
38	chr22:31889592-31889642	GM06990	blood:	n/a
39	chr22:31892562-31892612	AG09309	skin:	n/a
40	chr22:31892074-31892124	ovcar-3	ovarian:	n/a
41	chr22:31891804-31891854	HCPEpiC	choroid plexus:	n/a
42	chr22:31892343-31892393	HUVEC	blood vessel:	n/a
43	chr22:31892114-31892164	PFSK-1	brain:	n/a
44	chr22:31892152-31892202	GM06990	blood:	n/a
45	chr22:31892053-31892103	AG10803	skin:	n/a
46	chr22:31893096-31893146	BE2_C	brain:	n/a
47	chr22:31892793-31892843	HIPEpiC	eye:	n/a
48	chr22:31892114-31892164	NHBE	bronchial:	n/a
49	chr22:31893238-31893288	Caco-2	colon:	n/a
50	chr22:31892074-31892124	AG09309	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:31892596..31895248-chr22:31897166..31900535,3	MCF-7	breast:
2	chr22:31901562..31903154-chr22:32024706..32027058,2	MCF-7	breast:
3	chr22:31892596..31895248-chr22:31897166..31900535,3	MCF-7	breast:
4	chr22:31895925..31897585-chr22:31899327..31902230,2	K562	blood:
5	chr22:31895644..31897585-chr22:31899488..31902230,2	K562	blood:
6	chr22:31890586..31892478-chr6:26238591..26241305,2	MCF-7	breast:
7	chr22:31892881..31894794-chr22:31897314..31900016,2	K562	blood:
8	chr22:31895925..31897585-chr22:31899327..31902230,2	K562	blood:
9	chr22:31892433..31894421-chr22:31898516..31901632,3	K562	blood:
10	chr22:31890350..31892385-chr22:32144551..32147460,2	K562	blood:
11	chr22:31884404..31886896-chr22:31898271..31902090,3	MCF-7	breast:
12	chr22:31895644..31897585-chr22:31899488..31902230,2	K562	blood:
13	22:31864703-31891033..22:32347255-32351014	K562	blood:
14	chr11:18416054..18416559-chr22:31892154..31892989,2	Hela-S3	cervix:
15	22:31864703-31891033..22:31930706-31935473	GM12878	blood:
16	chr22:31891360..31893218-chr22:32058204..32060412,2	MCF-7	breast:
17	22:31864703-31891033..22:31936958-31958600	GM12878	blood:
18	chr22:31883080..31888273-chr22:31897152..31901136,10	MCF-7	breast:
19	chr22:31892695..31894776-chr22:32016253..32018919,2	K562	blood:
20	chr22:31892881..31894794-chr22:31897314..31900016,2	K562	blood:
21	chr22:31907252..31908998-chr22:32028816..32030585,2	MCF-7	breast:
22	chr22:31849740..31852347-chr22:31891078..31892965,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SFI1-2	chr22:31904241-31904362	NONHSAT084896
2	lnc-SFI1-2	chr22:31904241-31904362	NONHSAT084895
3	lnc-SFI1-2	chr22:31892450-31892623	NONHSAT084896

No data

Variant related genes	Relation type
EIF4ENIF1	TF binding region
SFI1	TF binding region
EIF4ENIF1	CpG island
SFI1	CpG island
ENSG00000238910	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000183530	chromatin interactions
ENSG00000184708	chromatin interactions
ENSG00000240591	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000198327	chromatin interactions
ENSG00000229169	chromatin interactions
ENSG00000214093	chromatin interactions
ENSG00000198089	chromatin interactions

Extended variants
information (count: 787 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141940895	chr22:31889224-31889225	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs541895658	chr22:31889252-31889253	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs562002161	chr22:31889306-31889307	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs533625065	chr22:31889353-31889354	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs181694490	chr22:31889356-31889357	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs564354476	chr22:31889379-31889380	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs533394538	chr22:31889410-31889411	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs186705735	chr22:31889504-31889505	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs190018147	chr22:31889529-31889530	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs145738733	chr22:31889546-31889547	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs74279029	chr22:31889547-31889548	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs182268639	chr22:31889557-31889558	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs568316895	chr22:31889562-31889563	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs5998011	chr22:31889566-31889567	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs557160963	chr22:31889570-31889571	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs78954132	chr22:31889588-31889589	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs74279031	chr22:31889592-31889593	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs373663140	chr22:31889621-31889622	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs377702991	chr22:31889665-31889666	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs573262479	chr22:31889670-31889671	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs542160051	chr22:31889693-31889694	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs555362647	chr22:31889700-31889701	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs186528107	chr22:31889711-31889712	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs544487625	chr22:31889785-31889786	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs564468578	chr22:31889786-31889787	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs533570361	chr22:31889794-31889795	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs75065229	chr22:31889823-31889824	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs576379206	chr22:31889843-31889844	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs5998012	chr22:31889844-31889845	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs548183413	chr22:31889870-31889871	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs568080654	chr22:31889937-31889938	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs138676821	chr22:31889950-31889951	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs78000282	chr22:31889980-31889981	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs5998013	chr22:31889981-31889982	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs73398237	chr22:31890034-31890035	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs10212025	chr22:31890055-31890056	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs546479062	chr22:31890060-31890061	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs12168003	chr22:31890065-31890066	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs10212027	chr22:31890070-31890071	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs111669682	chr22:31890120-31890121	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs66825611	chr22:31890136-31890137	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs138029277	chr22:31890155-31890156	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs547068383	chr22:31890181-31890182	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs560338149	chr22:31890185-31890186	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs535592270	chr22:31890286-31890287	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs371355708	chr22:31890299-31890300	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs578093203	chr22:31890300-31890301	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs398036887	chr22:31890312-31890313	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs532646635	chr22:31890318-31890319	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs190920789	chr22:31890326-31890327	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
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
Acute myeloid leukemia	20729466	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
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	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	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	17142309	CNVD
Autism	22543975	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:974 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31886800-31890200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr22:31887000-31889800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr22:31887000-31890600	Weak transcription	Psoas Muscle	Psoas
4	chr22:31887000-31891400	Weak transcription	Left Ventricle	heart
5	chr22:31887000-31891400	Weak transcription	Right Atrium	heart
6	chr22:31887000-31891600	Weak transcription	Right Ventricle	heart
7	chr22:31887000-31892000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr22:31887000-31892000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr22:31887000-31892000	Weak transcription	Lung	lung
10	chr22:31887000-31892000	Weak transcription	Pancreas	Pancrea
11	chr22:31887200-31890200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr22:31887200-31891200	Weak transcription	Fetal Stomach	stomach
13	chr22:31887200-31891400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr22:31887200-31891400	Weak transcription	Colonic Mucosa	Colon
15	chr22:31887200-31891400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr22:31887200-31891400	Weak transcription	Thymus	Thymus
17	chr22:31887200-31891600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr22:31887200-31891600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr22:31887200-31891600	Weak transcription	Stomach Mucosa	stomach
20	chr22:31887200-31892000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr22:31887400-31889600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr22:31887400-31889800	Weak transcription	Fetal Heart	heart
23	chr22:31887400-31891200	Weak transcription	Fetal Intestine Small	intestine
24	chr22:31887400-31891200	Weak transcription	Stomach Smooth Muscle	stomach
25	chr22:31887400-31891400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr22:31887400-31891400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr22:31887400-31891400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr22:31887400-31891400	Weak transcription	Adipose Nuclei	Adipose
29	chr22:31887400-31891400	Weak transcription	Brain Angular Gyrus	brain
30	chr22:31887400-31891400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr22:31887400-31891400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr22:31887400-31891400	Weak transcription	Hela-S3	cervix
33	chr22:31887400-31891600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr22:31887400-31891600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr22:31887400-31891600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr22:31887400-31891600	Weak transcription	Brain Substantia Nigra	brain
37	chr22:31887400-31891600	Weak transcription	Fetal Brain Male	brain
38	chr22:31887400-31891600	Weak transcription	Fetal Kidney	kidney
39	chr22:31887400-31891600	Weak transcription	Fetal Lung	lung
40	chr22:31887400-31891600	Weak transcription	A549	lung
41	chr22:31887400-31891600	Weak transcription	HMEC	breast
42	chr22:31887400-31891600	Weak transcription	HSMM	muscle
43	chr22:31887400-31891600	Weak transcription	HSMMtube	muscle
44	chr22:31887400-31891600	Weak transcription	NH-A	brain
45	chr22:31887400-31891600	Weak transcription	NHDF-Ad	bronchial
46	chr22:31887400-31891600	Weak transcription	Osteobl	bone
47	chr22:31887400-31891800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr22:31887400-31892000	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr22:31887400-31892000	Weak transcription	Spleen	Spleen
50	chr22:31887600-31889800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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