Variant report

Variant	nsv529886
Chromosome Location	chr22:34153740-34258847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:687)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:687 , 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	chr22:34181226-34181686	GM12878	blood:	n/a	n/a
3	ATF2	chr22:34183601-34184137	GM12878	blood:	n/a	n/a
4	ATF2	chr22:34183459-34184387	GM12878	blood:	n/a	n/a
5	ATF2	chr22:34237716-34238353	GM12878	blood:	n/a	n/a
6	ATF2	chr22:34185841-34186312	GM12878	blood:	n/a	n/a
7	ATF2	chr22:34237683-34238915	GM12878	blood:	n/a	n/a
8	ATF2	chr22:34185755-34186363	GM12878	blood:	n/a	n/a
9	BACH1	chr22:34225564-34225840	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr22:34221773-34221807	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr22:34244328-34244642	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr22:34185847-34186124	GM12878	blood:	n/a	n/a
13	BATF	chr22:34237726-34237991	GM12878	blood:	n/a	n/a
14	BATF	chr22:34184057-34184349	GM12878	blood:	n/a	n/a
15	BATF	chr22:34244253-34244653	GM12878	blood:	n/a	chr22:34244450-34244461
16	BATF	chr22:34185838-34186311	GM12878	blood:	n/a	n/a
17	BATF	chr22:34183589-34183875	GM12878	blood:	n/a	n/a
18	BATF	chr22:34154766-34154993	GM12878	blood:	n/a	n/a
19	BCL11A	chr22:34183569-34183918	GM12878	blood:	n/a	n/a
20	BCL3	chr22:34153825-34154068	GM12878	blood:	n/a	n/a
21	BCL3	chr22:34185878-34186387	GM12878	blood:	n/a	n/a
22	BCLAF1	chr22:34181218-34181676	GM12878	blood:	n/a	n/a
23	BCLAF1	chr22:34185839-34186424	GM12878	blood:	n/a	n/a
24	BCLAF1	chr22:34183553-34184056	GM12878	blood:	n/a	n/a
25	BCLAF1	chr22:34238364-34238878	GM12878	blood:	n/a	n/a
26	BCLAF1	chr22:34237755-34238277	GM12878	blood:	n/a	n/a
27	BCLAF1	chr22:34183601-34183918	GM12878	blood:	n/a	n/a
28	BHLHE40	chr22:34168931-34169192	GM12878	blood:	n/a	n/a
29	BHLHE40	chr22:34185856-34186187	GM12878	blood:	n/a	n/a
30	BHLHE40	chr22:34202110-34202534	GM12878	blood:	n/a	n/a
31	CEBPB	chr22:34160038-34160378	HepG2	liver:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
32	CEBPB	chr22:34244733-34245063	IMR90	lung:	n/a	chr22:34244894-34244905
33	CEBPB	chr22:34237675-34238915	GM12878	blood:	n/a	n/a
34	CEBPB	chr22:34257611-34257827	HepG2	liver:	n/a	chr22:34257719-34257730
35	CEBPB	chr22:34235669-34235930	HepG2	liver:	n/a	n/a
36	CEBPB	chr22:34160056-34160345	A549	lung:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
37	CEBPB	chr22:34153833-34154197	HepG2	liver:	n/a	n/a
38	CEBPB	chr22:34194364-34194659	HepG2	liver:	n/a	chr22:34194414-34194427
39	CEBPB	chr22:34160080-34160369	IMR90	lung:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
40	CEBPB	chr22:34181187-34181655	IMR90	lung:	n/a	n/a
41	CEBPB	chr22:34160073-34160312	H1-hESC	embryonic stem cell:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
42	CEBPB	chr22:34235773-34235879	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr22:34235119-34235472	IMR90	lung:	n/a	n/a
44	CEBPB	chr22:34257515-34257838	MCF-7	breast:	n/a	chr22:34257719-34257730
45	CEBPB	chr22:34177308-34177537	IMR90	lung:	n/a	n/a
46	CEBPB	chr22:34244798-34244998	HepG2	liver:	n/a	chr22:34244894-34244905
47	CEBPB	chr22:34217100-34217196	HepG2	liver:	n/a	chr22:34217123-34217134
48	CEBPB	chr22:34244767-34245053	H1-hESC	embryonic stem cell:	n/a	chr22:34244894-34244905
49	CEBPB	chr22:34257735-34257755	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr22:34257657-34257790	K562	blood:	n/a	chr22:34257719-34257730

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34192387-34192437	K562	blood:	n/a
2	chr22:34192387-34192437	SAEC	small airway:	n/a
3	chr22:34192387-34192437	AG09319	gingival:	n/a
4	chr22:34192387-34192437	AoSMC	blood vessel:	n/a
5	chr22:34192387-34192437	LNCaP	prostate:	n/a
6	chr22:34192387-34192437	NT2-D1	testis:	n/a
7	chr22:34192387-34192437	HRPEpiC	eye:	n/a
8	chr22:34192387-34192437	MCF10A-Er-Src	breast:	n/a
9	chr22:34192387-34192437	AG10803	skin:	n/a
10	chr22:34192387-34192437	Caco-2	colon:	n/a
11	chr22:34192387-34192437	IMR90	lung:	fetal
12	chr22:34192387-34192437	RPTEC	kidney:	n/a
13	chr22:34192387-34192437	AG04450	lung:	fetal
14	chr22:34192387-34192437	GM06990	blood:	n/a
15	chr22:34192387-34192437	BJ	skin:	n/a
16	chr22:34192387-34192437	MCF-7	breast:	n/a
17	chr22:34192387-34192437	HRE	kidney:	n/a
18	chr22:34192387-34192437	HUVEC	blood vessel:	n/a
19	chr22:34192387-34192437	SKMC	muscle:	n/a
20	chr22:34192387-34192437	BE2_C	brain:	n/a
21	chr22:34192387-34192437	GM19239	blood:	n/a
22	chr22:34192387-34192437	PFSK-1	brain:	n/a
23	chr22:34192387-34192437	HCM	heart:	n/a
24	chr22:34192387-34192437	GM12878	blood:	n/a
25	chr22:34192387-34192437	HL-60	blood:	n/a
26	chr22:34192387-34192437	HRCEpiC	kidney:	n/a
27	chr22:34192387-34192437	U87	brain:	n/a
28	chr22:34192387-34192437	SK-N-SH	brain:	n/a
29	chr22:34192387-34192437	HCF	heart:	n/a
30	chr22:34192387-34192437	NH-A	brain:	n/a
31	chr22:34192387-34192437	HAEpiC	amniotic membrane:	n/a
32	chr22:34192387-34192437	PANC-1	pancreas:	n/a
33	chr22:34192387-34192437	HMEC	breast:	n/a
34	chr22:34192387-34192437	CMK	blood:	n/a
35	chr22:34192387-34192437	A549	lung:	n/a
36	chr22:34192387-34192437	Jurkat	blood:	n/a
37	chr22:34192387-34192437	NB4	blood:	n/a
38	chr22:34192387-34192437	HIPEpiC	eye:	n/a
39	chr22:34192387-34192437	SK-N-SH_RA	brain:	n/a
40	chr22:34192387-34192437	ovcar-3	ovarian:	n/a
41	chr22:34192387-34192437	Hela-S3	cervix:	n/a
42	chr22:34192387-34192437	AG04449	skin:	fetal
43	chr22:34192387-34192437	HNPCEpiC	eye:	n/a
44	chr22:34192387-34192437	HEK293	kidney:	embryo
45	chr22:34192387-34192437	H1-hESC	embryonic stem cell:	embryo
46	chr22:34192387-34192437	HCT-116	colon:	n/a
47	chr22:34192387-34192437	HEEpiC	esophagus:	n/a
48	chr22:34192387-34192437	T-47D	breast:	n/a
49	chr22:34192387-34192437	ProgFib	skin:	n/a
50	chr22:34192387-34192437	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
2	chr22:34247996..34248570-chr22:34261032..34261815,2	MCF-7	breast:
3	chr22:34172664..34173221-chr22:34313368..34314036,2	MCF-7	breast:
4	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
5	chr22:34255630..34257426-chr22:34307549..34309607,2	MCF-7	breast:
6	chr22:34246562..34250566-chr22:34253925..34258689,11	MCF-7	breast:
7	chr22:34248614..34251924-chr22:34259957..34262591,3	MCF-7	breast:
8	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:
9	chr22:34248240..34252170-chr22:34315347..34319641,4	MCF-7	breast:
10	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
11	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
12	chr22:34181411..34183196-chr22:34314966..34317332,2	MCF-7	breast:
13	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
14	chr22:34243203..34243910-chr9:5087187..5087998,2	MCF-7	breast:
15	chr22:34245347..34248923-chr22:34315491..34319689,7	MCF-7	breast:
16	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
17	chr22:34255666..34258346-chr22:34316396..34318049,2	MCF-7	breast:
18	chr22:34248231..34249994-chr22:34261049..34263874,2	MCF-7	breast:
19	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
20	chr22:34247616..34248584-chr22:34315645..34316533,2	MCF-7	breast:
21	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
22	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:

No data

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

Extended variants
information (count: 4654 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4654 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs481698	chr22:34153779-34153780	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143618248	chr22:34153782-34153783	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554733525	chr22:34153783-34153784	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs715482	chr22:34153788-34153789	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs543094369	chr22:34153789-34153790	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147227738	chr22:34153823-34153824	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576718874	chr22:34153824-34153825	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185588285	chr22:34153851-34153852	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35458107	chr22:34153853-34153854	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs482567	chr22:34153854-34153855	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs573127119	chr22:34153963-34153964	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs483528	chr22:34153966-34153967	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537154299	chr22:34153981-34153982	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531031560	chr22:34153984-34153985	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550750662	chr22:34153992-34153993	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564515838	chr22:34153998-34153999	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2283940	chr22:34154020-34154021	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs529609998	chr22:34154076-34154077	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552468926	chr22:34154095-34154096	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367778869	chr22:34154121-34154122	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140585957	chr22:34154122-34154123	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534851695	chr22:34154138-34154139	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191141720	chr22:34154185-34154186	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs110689	chr22:34154229-34154230	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1008501	chr22:34154285-34154286	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs34071097	chr22:34154303-34154304	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530648851	chr22:34154331-34154332	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556745024	chr22:34154333-34154334	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376585736	chr22:34154369-34154370	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562497283	chr22:34154370-34154371	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34161416	chr22:34154375-34154376	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144481856	chr22:34154381-34154382	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111628534	chr22:34154401-34154402	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573190210	chr22:34154433-34154434	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs5999089	chr22:34154444-34154445	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183107673	chr22:34154468-34154469	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs417683	chr22:34154474-34154475	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs544709442	chr22:34154540-34154541	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564397240	chr22:34154621-34154622	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373526514	chr22:34154645-34154646	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376402733	chr22:34154660-34154661	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561778639	chr22:34154661-34154662	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556753311	chr22:34154705-34154706	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150617701	chr22:34154713-34154714	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530286377	chr22:34154716-34154717	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368455290	chr22:34154720-34154721	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559728175	chr22:34154754-34154755	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547147902	chr22:34154755-34154756	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139668054	chr22:34154795-34154796	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548460845	chr22:34154798-34154799	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34124800-34171000	Weak transcription	Ovary	ovary
2	chr22:34126200-34176200	Weak transcription	Spleen	Spleen
3	chr22:34131000-34154200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr22:34134400-34164800	Weak transcription	Brain Anterior Caudate	brain
5	chr22:34138000-34160800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr22:34143400-34160000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr22:34145000-34154000	Weak transcription	Primary B cells from peripheral blood	blood
8	chr22:34147400-34158400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr22:34147400-34168600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr22:34147600-34154600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr22:34149200-34167000	Weak transcription	Brain Angular Gyrus	brain
12	chr22:34150800-34154800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr22:34150800-34155000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr22:34151000-34155000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr22:34151400-34155600	Enhancers	Fetal Heart	heart
16	chr22:34151800-34155000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr22:34151800-34159000	Weak transcription	Fetal Intestine Large	intestine
18	chr22:34151800-34167000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr22:34152000-34158400	Weak transcription	Fetal Intestine Small	intestine
20	chr22:34152200-34156800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr22:34152400-34154400	Enhancers	Fetal Muscle Leg	muscle
22	chr22:34152400-34154400	Genic enhancers	Fetal Stomach	stomach
23	chr22:34152400-34154600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr22:34152400-34154600	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr22:34152400-34155000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr22:34152400-34155400	Enhancers	Liver	Liver
27	chr22:34152600-34154200	Enhancers	Rectal Smooth Muscle	rectum
28	chr22:34152600-34154400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr22:34152600-34154400	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr22:34152600-34154600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr22:34152600-34154600	Enhancers	Right Ventricle	heart
32	chr22:34152600-34154800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr22:34152600-34154800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr22:34152600-34154800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr22:34152600-34154800	Enhancers	Left Ventricle	heart
36	chr22:34152600-34155200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr22:34152800-34154200	Enhancers	Fetal Kidney	kidney
38	chr22:34152800-34154400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr22:34152800-34154400	Enhancers	Colon Smooth Muscle	Colon
40	chr22:34152800-34154600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr22:34152800-34154600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr22:34153000-34154000	Weak transcription	Gastric	stomach
43	chr22:34153200-34154200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr22:34153200-34154200	Enhancers	Psoas Muscle	Psoas
45	chr22:34153200-34164800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr22:34153400-34153800	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr22:34153400-34154000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr22:34153400-34158400	Weak transcription	Aorta	Aorta
49	chr22:34153400-34169000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr22:34153600-34154000	Weak transcription	Pancreas	Pancrea

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