Variant report

Variant	nsv1055203
Chromosome Location	chr22:34098417-34196685
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:504)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:88)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr22:34183601-34184137	GM12878	blood:	n/a	n/a
2	ATF2	chr22:34181226-34181686	GM12878	blood:	n/a	n/a
3	ATF2	chr22:34185841-34186312	GM12878	blood:	n/a	n/a
4	ATF2	chr22:34183459-34184387	GM12878	blood:	n/a	n/a
5	ATF2	chr22:34185755-34186363	GM12878	blood:	n/a	n/a
6	BACH1	chr22:34135101-34135251	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr22:34154766-34154993	GM12878	blood:	n/a	n/a
8	BATF	chr22:34185847-34186124	GM12878	blood:	n/a	n/a
9	BATF	chr22:34183589-34183875	GM12878	blood:	n/a	n/a
10	BATF	chr22:34184057-34184349	GM12878	blood:	n/a	n/a
11	BATF	chr22:34185838-34186311	GM12878	blood:	n/a	n/a
12	BCL11A	chr22:34183569-34183918	GM12878	blood:	n/a	n/a
13	BCL3	chr22:34139772-34140140	GM12878	blood:	n/a	n/a
14	BCL3	chr22:34153825-34154068	GM12878	blood:	n/a	n/a
15	BCL3	chr22:34185878-34186387	GM12878	blood:	n/a	n/a
16	BCLAF1	chr22:34181218-34181676	GM12878	blood:	n/a	n/a
17	BCLAF1	chr22:34183601-34183918	GM12878	blood:	n/a	n/a
18	BCLAF1	chr22:34183553-34184056	GM12878	blood:	n/a	n/a
19	BCLAF1	chr22:34185839-34186424	GM12878	blood:	n/a	n/a
20	BHLHE40	chr22:34119934-34120194	GM12878	blood:	n/a	n/a
21	BHLHE40	chr22:34114028-34114321	HepG2	liver:	n/a	n/a
22	BHLHE40	chr22:34168931-34169192	GM12878	blood:	n/a	n/a
23	BHLHE40	chr22:34185856-34186187	GM12878	blood:	n/a	n/a
24	CEBPB	chr22:34194364-34194659	HepG2	liver:	n/a	chr22:34194414-34194427
25	CEBPB	chr22:34181187-34181655	IMR90	lung:	n/a	n/a
26	CEBPB	chr22:34160073-34160312	H1-hESC	embryonic stem cell:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
27	CEBPB	chr22:34153833-34154197	HepG2	liver:	n/a	n/a
28	CEBPB	chr22:34142598-34142923	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
29	CEBPB	chr22:34142582-34142926	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
30	CEBPB	chr22:34142642-34142976	A549	lung:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
31	CEBPB	chr22:34142695-34142833	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	chr22:34177308-34177537	IMR90	lung:	n/a	n/a
34	CEBPB	chr22:34160080-34160369	IMR90	lung:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
35	CEBPB	chr22:34160038-34160378	HepG2	liver:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
36	CHD2	chr22:34165725-34165749	GM12878	blood:	n/a	n/a
37	CTCF	chr22:34172980-34173130	HCPEpiC	choroid plexus:	n/a	chr22:34173068-34173084 chr22:34173067-34173085 chr22:34173069-34173090
38	CTCF	chr22:34102228-34102527	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr22:34152604-34152615	A549	lung:	n/a	n/a
40	CTCF	chr22:34192580-34192730	GM12866	blood:	n/a	n/a
41	CTCF	chr22:34112658-34112721	GM10248	blood:	n/a	n/a
42	CTCF	chr22:34192300-34192450	NHEK	skin:	n/a	n/a
43	CTCF	chr22:34173040-34173190	AG04449	skin:	n/a	chr22:34173068-34173084 chr22:34173067-34173085 chr22:34173069-34173090
44	CTCF	chr22:34152560-34152710	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr22:34175584-34175616	Lung_OC	lung:	n/a	n/a
46	CTCF	chr22:34192580-34192730	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr22:34192540-34192690	Caco-2	colon:	n/a	n/a
48	CTCF	chr22:34152508-34152680	GM19239	blood:	n/a	n/a
49	CTCF	chr22:34152493-34152651	GM12878	blood:	n/a	n/a
50	CTCF	chr22:34192580-34192730	HEK293	kidney:	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	PANC-1	pancreas:	n/a
2	chr22:34192387-34192437	HNPCEpiC	eye:	n/a
3	chr22:34192387-34192437	Jurkat	blood:	n/a
4	chr22:34192387-34192437	Hela-S3	cervix:	n/a
5	chr22:34192387-34192437	RPTEC	kidney:	n/a
6	chr22:34192387-34192437	BJ	skin:	n/a
7	chr22:34192387-34192437	SAEC	small airway:	n/a
8	chr22:34192387-34192437	HUVEC	blood vessel:	n/a
9	chr22:34192387-34192437	SKMC	muscle:	n/a
10	chr22:34192387-34192437	K562	blood:	n/a
11	chr22:34192387-34192437	MCF10A-Er-Src	breast:	n/a
12	chr22:34192387-34192437	HRE	kidney:	n/a
13	chr22:34192387-34192437	NHDF-neo	bronchial:	n/a
14	chr22:34192387-34192437	HEK293	kidney:	embryo
15	chr22:34192387-34192437	HRCEpiC	kidney:	n/a
16	chr22:34192387-34192437	A549	lung:	n/a
17	chr22:34192387-34192437	NB4	blood:	n/a
18	chr22:34192387-34192437	NHBE	bronchial:	n/a
19	chr22:34192387-34192437	HCF	heart:	n/a
20	chr22:34192387-34192437	SK-N-MC	brain:	n/a
21	chr22:34192387-34192437	GM19239	blood:	n/a
22	chr22:34192387-34192437	U87	brain:	n/a
23	chr22:34192387-34192437	ovcar-3	ovarian:	n/a
24	chr22:34192387-34192437	AG04449	skin:	fetal
25	chr22:34192387-34192437	GM12891	blood:	n/a
26	chr22:34192387-34192437	HepG2	liver:	n/a
27	chr22:34192387-34192437	AG09319	gingival:	n/a
28	chr22:34192387-34192437	ProgFib	skin:	n/a
29	chr22:34192387-34192437	H1-hESC	embryonic stem cell:	embryo
30	chr22:34192387-34192437	Hepatocyte	liver:	n/a
31	chr22:34192387-34192437	HCM	heart:	n/a
32	chr22:34192387-34192437	HIPEpiC	eye:	n/a
33	chr22:34192387-34192437	SK-N-SH_RA	brain:	n/a
34	chr22:34192387-34192437	Caco-2	colon:	n/a
35	chr22:34192387-34192437	HMEC	breast:	n/a
36	chr22:34192387-34192437	GM06990	blood:	n/a
37	chr22:34192387-34192437	AG09309	skin:	n/a
38	chr22:34192387-34192437	ECC-1	luminal epithelium:	n/a
39	chr22:34192387-34192437	LNCaP	prostate:	n/a
40	chr22:34192387-34192437	NH-A	brain:	n/a
41	chr22:34192387-34192437	PrEC	prostate:	n/a
42	chr22:34192387-34192437	GM12878	blood:	n/a
43	chr22:34192387-34192437	GM12892	blood:	n/a
44	chr22:34192387-34192437	NT2-D1	testis:	n/a
45	chr22:34192387-34192437	T-47D	breast:	n/a
46	chr22:34192387-34192437	HAEpiC	amniotic membrane:	n/a
47	chr22:34192387-34192437	HCPEpiC	choroid plexus:	n/a
48	chr22:34192387-34192437	BE2_C	brain:	n/a
49	chr22:34192387-34192437	AG04450	lung:	fetal
50	chr22:34192387-34192437	MCF-7	breast:	n/a

(count:8 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085018
2	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085014
3	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
4	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
5	lnc-TIMP3-6	chr22:34139996-34140315	ENSG00000224973.1
6	lnc-TIMP3-6	chr22:34139122-34139185	ENSG00000224973.1
7	lnc-TIMP3-6	chr22:34121003-34121087	NONHSAT085014
8	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
9	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
10	lnc-TIMP3-6	chr22:34121055-34121087	ENSG00000224973.1
11	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085018
12	lnc-TIMP3-6	chr22:34128242-34128488	ENSG00000224973.1
13	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1
14	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085015
15	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085014
16	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085013
17	lnc-TIMP3-6	chr22:34121003-34121087	NONHSAT085015
18	lnc-TIMP3-6	chr22:34121058-34121087	ENSG00000224973.1
19	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
20	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085014
21	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085014
22	lnc-TIMP3-6	chr22:34146591-34146670	ENSG00000224973.1
23	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085013
24	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085011
25	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085015
26	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085011
27	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085015
28	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085015
29	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085012
30	lnc-TIMP3-6	chr22:34133550-34133769	ENSG00000224973.1
31	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085011
32	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085012
33	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085018
34	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085015
35	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085011
36	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085014
37	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1
38	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
39	lnc-TIMP3-6	chr22:34123477-34123574	ENSG00000224973.1
40	lnc-TIMP3-6	chr22:34146591-34146803	NONHSAT085012
41	lnc-TIMP3-6	chr22:34146591-34146644	ENSG00000224973.1
42	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085012
43	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
44	lnc-TIMP3-6	chr22:34142402-34142444	ENSG00000224973.1
45	lnc-SYN3-4	chr22:34119818-34120265	ENSG00000232081.1
46	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
47	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085011
48	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
49	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085014
50	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085012

No data

Variant related genes	Relation type
LARGE-AS1	TF binding region
ENSG00000253007	TF binding region
LARGE-IT1	TF binding region
LARGE-AS1	CpG island
ENSG00000253007	CpG island
LARGE-IT1	CpG island
ENSG00000133424	chromatin interactions
ENSG00000273082	chromatin interactions

Extended variants
information (count: 4376 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4376 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs240082	chr22:34098417-34098418	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548071780	chr22:34098491-34098492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147292280	chr22:34098512-34098513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184829526	chr22:34098521-34098522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575012915	chr22:34098523-34098524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537227742	chr22:34098563-34098564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116260587	chr22:34098617-34098618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549429350	chr22:34098724-34098725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112408162	chr22:34098830-34098831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9607074	chr22:34098888-34098889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9607075	chr22:34098919-34098920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377635056	chr22:34098921-34098922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577409273	chr22:34098941-34098942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546278626	chr22:34098949-34098950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189773294	chr22:34098960-34098961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573238982	chr22:34098992-34098993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs240083	chr22:34099055-34099056	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs138002373	chr22:34099093-34099094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539516891	chr22:34099094-34099095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111264704	chr22:34099119-34099120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543499017	chr22:34099125-34099126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180968118	chr22:34099127-34099128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532078973	chr22:34099164-34099165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75497523	chr22:34099194-34099195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555195162	chr22:34099272-34099273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35323382	chr22:34099315-34099316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79997713	chr22:34099342-34099343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565355879	chr22:34099351-34099352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74988188	chr22:34099357-34099358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373791100	chr22:34099358-34099359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186082928	chr22:34099363-34099364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528064075	chr22:34099402-34099403	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs548893803	chr22:34099427-34099428	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs568658074	chr22:34099428-34099429	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs147186851	chr22:34099454-34099455	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs557282190	chr22:34099457-34099458	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs372302379	chr22:34099459-34099460	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs62225377	chr22:34099520-34099521	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs539955165	chr22:34099533-34099534	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs116973887	chr22:34099539-34099540	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs573301909	chr22:34099563-34099564	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs541854456	chr22:34099585-34099586	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs554887470	chr22:34099612-34099613	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs189492253	chr22:34099669-34099670	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs36105409	chr22:34099690-34099691	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs370437464	chr22:34099705-34099706	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs563162277	chr22:34099723-34099724	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs545879115	chr22:34099726-34099727	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs532144053	chr22:34099800-34099801	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs115649226	chr22:34099843-34099844	Weak transcription ZNF genes & repeats	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1305 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34075000-34100400	Weak transcription	Brain Anterior Caudate	brain
2	chr22:34076200-34106400	Weak transcription	Psoas Muscle	Psoas
3	chr22:34081800-34098800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr22:34085600-34103600	Weak transcription	Colon Smooth Muscle	Colon
5	chr22:34087000-34109400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr22:34089800-34099600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr22:34090400-34100200	Weak transcription	Aorta	Aorta
8	chr22:34090800-34099400	Weak transcription	Esophagus	oesophagus
9	chr22:34091600-34115800	Weak transcription	Pancreas	Pancrea
10	chr22:34092400-34109200	Weak transcription	Fetal Intestine Large	intestine
11	chr22:34093800-34098600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr22:34094000-34099400	Weak transcription	Duodenum Mucosa	Duodenum
13	chr22:34094200-34098800	Weak transcription	HepG2	liver
14	chr22:34094400-34102200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr22:34095600-34099200	Weak transcription	Fetal Muscle Leg	muscle
16	chr22:34096400-34103200	Weak transcription	GM12878-XiMat	blood
17	chr22:34097000-34098800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr22:34097000-34099000	Enhancers	Fetal Heart	heart
19	chr22:34097000-34110000	Weak transcription	Ovary	ovary
20	chr22:34097200-34098800	Enhancers	Right Ventricle	heart
21	chr22:34097200-34101200	Weak transcription	Gastric	stomach
22	chr22:34097200-34102200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr22:34097200-34103400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr22:34097200-34108000	Weak transcription	Fetal Intestine Small	intestine
25	chr22:34097200-34109200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr22:34097200-34109200	Weak transcription	Fetal Brain Female	brain
27	chr22:34097200-34109400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr22:34097400-34099000	Enhancers	Left Ventricle	heart
29	chr22:34097400-34103200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr22:34097400-34107400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr22:34097600-34100400	Weak transcription	Liver	Liver
32	chr22:34097600-34102400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr22:34097600-34110200	Weak transcription	Stomach Smooth Muscle	stomach
34	chr22:34097600-34114600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr22:34097800-34099200	Weak transcription	Brain Hippocampus Middle	brain
36	chr22:34097800-34099600	Weak transcription	Primary B cells from peripheral blood	blood
37	chr22:34097800-34099600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr22:34097800-34100200	Weak transcription	Right Atrium	heart
39	chr22:34097800-34105400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr22:34098000-34102200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr22:34098200-34098800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr22:34098200-34098800	Enhancers	Lung	lung
43	chr22:34098200-34099000	Weak transcription	Spleen	Spleen
44	chr22:34098200-34099400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr22:34098200-34099600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr22:34098200-34110600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr22:34098400-34098600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr22:34098400-34099000	Enhancers	Adipose Nuclei	Adipose
49	chr22:34098400-34099600	Weak transcription	Fetal Stomach	stomach
50	chr22:34098400-34100200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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