Variant report

Variant	nsv524156
Chromosome Location	chr22:34145596-34260738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:811)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:34260707-34261720	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:34219541-34219836	HepG2	liver:	n/a	n/a
3	ATF2	chr22:34185755-34186363	GM12878	blood:	n/a	n/a
4	ATF2	chr22:34181226-34181686	GM12878	blood:	n/a	n/a
5	ATF2	chr22:34237716-34238353	GM12878	blood:	n/a	n/a
6	ATF2	chr22:34183459-34184387	GM12878	blood:	n/a	n/a
7	ATF2	chr22:34185841-34186312	GM12878	blood:	n/a	n/a
8	ATF2	chr22:34237683-34238915	GM12878	blood:	n/a	n/a
9	ATF2	chr22:34183601-34184137	GM12878	blood:	n/a	n/a
10	BACH1	chr22:34225564-34225840	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr22:34221773-34221807	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr22:34244328-34244642	H1-hESC	embryonic stem cell:	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	chr22:34183589-34183875	GM12878	blood:	n/a	n/a
16	BATF	chr22:34154766-34154993	GM12878	blood:	n/a	n/a
17	BATF	chr22:34185838-34186311	GM12878	blood:	n/a	n/a
18	BATF	chr22:34244253-34244653	GM12878	blood:	n/a	chr22:34244450-34244461
19	BATF	chr22:34185847-34186124	GM12878	blood:	n/a	n/a
20	BCL11A	chr22:34183569-34183918	GM12878	blood:	n/a	n/a
21	BCL3	chr22:34185878-34186387	GM12878	blood:	n/a	n/a
22	BCL3	chr22:34153825-34154068	GM12878	blood:	n/a	n/a
23	BCLAF1	chr22:34181218-34181676	GM12878	blood:	n/a	n/a
24	BCLAF1	chr22:34183553-34184056	GM12878	blood:	n/a	n/a
25	BCLAF1	chr22:34237755-34238277	GM12878	blood:	n/a	n/a
26	BCLAF1	chr22:34238364-34238878	GM12878	blood:	n/a	n/a
27	BCLAF1	chr22:34183601-34183918	GM12878	blood:	n/a	n/a
28	BCLAF1	chr22:34185839-34186424	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	BHLHE40	chr22:34168931-34169192	GM12878	blood:	n/a	n/a
32	CEBPB	chr22:34235669-34235930	HepG2	liver:	n/a	n/a
33	CEBPB	chr22:34160080-34160369	IMR90	lung:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
34	CEBPB	chr22:34257611-34257827	HepG2	liver:	n/a	chr22:34257719-34257730
35	CEBPB	chr22:34181187-34181655	IMR90	lung:	n/a	n/a
36	CEBPB	chr22:34257515-34257838	MCF-7	breast:	n/a	chr22:34257719-34257730
37	CEBPB	chr22:34244733-34245063	IMR90	lung:	n/a	chr22:34244894-34244905
38	CEBPB	chr22:34177308-34177537	IMR90	lung:	n/a	n/a
39	CEBPB	chr22:34237675-34238915	GM12878	blood:	n/a	n/a
40	CEBPB	chr22:34194364-34194659	HepG2	liver:	n/a	chr22:34194414-34194427
41	CEBPB	chr22:34260670-34260959	HepG2	liver:	n/a	chr22:34260820-34260831
42	CEBPB	chr22:34160073-34160312	H1-hESC	embryonic stem cell:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
43	CEBPB	chr22:34260708-34260897	A549	lung:	n/a	chr22:34260820-34260831
44	CEBPB	chr22:34244798-34244998	HepG2	liver:	n/a	chr22:34244894-34244905
45	CEBPB	chr22:34257735-34257755	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr22:34217100-34217196	HepG2	liver:	n/a	chr22:34217123-34217134
47	CEBPB	chr22:34260635-34261548	HepG2	liver:	n/a	chr22:34260820-34260831
48	CEBPB	chr22:34244767-34245053	H1-hESC	embryonic stem cell:	n/a	chr22:34244894-34244905
49	CEBPB	chr22:34160038-34160378	HepG2	liver:	n/a	chr22:34160214-34160225 chr22:34160212-34160223
50	CEBPB	chr22:34260638-34261015	IMR90	lung:	n/a	chr22:34260820-34260831

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34192387-34192437	SK-N-MC	brain:	n/a
2	chr22:34192387-34192437	AG10803	skin:	n/a
3	chr22:34192387-34192437	RPTEC	kidney:	n/a
4	chr22:34192387-34192437	SK-N-SH	brain:	n/a
5	chr22:34192387-34192437	LNCaP	prostate:	n/a
6	chr22:34192387-34192437	HEK293	kidney:	embryo
7	chr22:34192387-34192437	CMK	blood:	n/a
8	chr22:34192387-34192437	HCPEpiC	choroid plexus:	n/a
9	chr22:34192387-34192437	GM12878	blood:	n/a
10	chr22:34192387-34192437	SAEC	small airway:	n/a
11	chr22:34192387-34192437	HL-60	blood:	n/a
12	chr22:34192387-34192437	BJ	skin:	n/a
13	chr22:34192387-34192437	MCF10A-Er-Src	breast:	n/a
14	chr22:34192387-34192437	HCT-116	colon:	n/a
15	chr22:34192387-34192437	GM12891	blood:	n/a
16	chr22:34192387-34192437	U87	brain:	n/a
17	chr22:34192387-34192437	AG09319	gingival:	n/a
18	chr22:34192387-34192437	MCF-7	breast:	n/a
19	chr22:34192387-34192437	HMEC	breast:	n/a
20	chr22:34192387-34192437	AG09309	skin:	n/a
21	chr22:34192387-34192437	HAEpiC	amniotic membrane:	n/a
22	chr22:34192387-34192437	T-47D	breast:	n/a
23	chr22:34192387-34192437	HRE	kidney:	n/a
24	chr22:34192387-34192437	HRPEpiC	eye:	n/a
25	chr22:34192387-34192437	AG04450	lung:	fetal
26	chr22:34192387-34192437	HCM	heart:	n/a
27	chr22:34192387-34192437	SK-N-SH_RA	brain:	n/a
28	chr22:34192387-34192437	Hepatocyte	liver:	n/a
29	chr22:34192387-34192437	GM12892	blood:	n/a
30	chr22:34192387-34192437	PANC-1	pancreas:	n/a
31	chr22:34192387-34192437	PFSK-1	brain:	n/a
32	chr22:34192387-34192437	HNPCEpiC	eye:	n/a
33	chr22:34192387-34192437	IMR90	lung:	fetal
34	chr22:34192387-34192437	NH-A	brain:	n/a
35	chr22:34192387-34192437	Jurkat	blood:	n/a
36	chr22:34192387-34192437	BE2_C	brain:	n/a
37	chr22:34192387-34192437	ProgFib	skin:	n/a
38	chr22:34192387-34192437	Caco-2	colon:	n/a
39	chr22:34192387-34192437	Hela-S3	cervix:	n/a
40	chr22:34192387-34192437	K562	blood:	n/a
41	chr22:34192387-34192437	NB4	blood:	n/a
42	chr22:34192387-34192437	AoSMC	blood vessel:	n/a
43	chr22:34192387-34192437	HUVEC	blood vessel:	n/a
44	chr22:34192387-34192437	GM06990	blood:	n/a
45	chr22:34192387-34192437	NHBE	bronchial:	n/a
46	chr22:34192387-34192437	HepG2	liver:	n/a
47	chr22:34192387-34192437	HRCEpiC	kidney:	n/a
48	chr22:34192387-34192437	ovcar-3	ovarian:	n/a
49	chr22:34192387-34192437	NT2-D1	testis:	n/a
50	chr22:34192387-34192437	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
2	chr22:34181411..34183196-chr22:34314966..34317332,2	MCF-7	breast:
3	chr22:34243203..34243910-chr9:5087187..5087998,2	MCF-7	breast:
4	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
5	chr22:34247996..34248570-chr22:34261032..34261815,2	MCF-7	breast:
6	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:
7	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
8	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
9	chr22:34260736..34263686-chr22:34313890..34318281,7	MCF-7	breast:
10	chr22:34259639..34261419-chr22:34267116..34269181,2	MCF-7	breast:
11	chr22:34255666..34258346-chr22:34316396..34318049,2	MCF-7	breast:
12	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
13	chr22:34248614..34251924-chr22:34259957..34262591,3	MCF-7	breast:
14	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
15	chr22:34248231..34249994-chr22:34261049..34263874,2	MCF-7	breast:
16	chr22:34248614..34251924-chr22:34259957..34262591,3	MCF-7	breast:
17	chr22:34245347..34248923-chr22:34315491..34319689,7	MCF-7	breast:
18	chr22:34247616..34248584-chr22:34315645..34316533,2	MCF-7	breast:
19	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
20	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
21	chr22:34172664..34173221-chr22:34313368..34314036,2	MCF-7	breast:
22	chr22:34246562..34250566-chr22:34253925..34258689,11	MCF-7	breast:
23	chr22:34255630..34257426-chr22:34307549..34309607,2	MCF-7	breast:
24	chr22:34248240..34252170-chr22:34315347..34319641,4	MCF-7	breast:
25	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIMP3-6	chr22:34146591-34146729	ENSG00000224973.1
2	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085018
3	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085015
4	lnc-TIMP3-6	chr22:34146591-34146803	NONHSAT085012
5	lnc-TIMP3-6	chr22:34146591-34146803	NONHSAT085011
6	lnc-TIMP3-6	chr22:34146591-34146830	ENSG00000224973.1
7	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085014
8	lnc-TIMP3-6	chr22:34146591-34146644	ENSG00000224973.1
9	lnc-TIMP3-6	chr22:34146591-34146670	ENSG00000224973.1

No data

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

Extended variants
information (count: 5088 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:5088 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11912486	chr22:34145596-34145597	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568646976	chr22:34145619-34145620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553594074	chr22:34145627-34145628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182401359	chr22:34145630-34145631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138476095	chr22:34145645-34145646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571229952	chr22:34145651-34145652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs5754655	chr22:34145663-34145664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533519452	chr22:34145668-34145669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73402876	chr22:34145711-34145712	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs574227362	chr22:34145747-34145748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536878132	chr22:34145748-34145749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556783732	chr22:34145749-34145750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186666949	chr22:34145750-34145751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12158212	chr22:34145775-34145776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565340646	chr22:34145779-34145780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572422254	chr22:34145805-34145806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12329992	chr22:34145831-34145832	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs558399266	chr22:34145865-34145866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372224566	chr22:34145872-34145873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12329999	chr22:34145873-34145874	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs529160673	chr22:34145929-34145930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542455113	chr22:34145950-34145951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143413497	chr22:34145982-34145983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531362199	chr22:34146118-34146119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192213808	chr22:34146124-34146125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369413746	chr22:34146126-34146127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373150670	chr22:34146129-34146130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527309650	chr22:34146139-34146140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375271516	chr22:34146156-34146157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs16992967	chr22:34146173-34146174	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs567987169	chr22:34146228-34146229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563663979	chr22:34146283-34146284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529352351	chr22:34146327-34146328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556846920	chr22:34146330-34146331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543098783	chr22:34146347-34146348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576862518	chr22:34146349-34146350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs5999086	chr22:34146368-34146369	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs148371501	chr22:34146376-34146377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73402881	chr22:34146410-34146411	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs528757843	chr22:34146412-34146413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554657437	chr22:34146448-34146449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551308811	chr22:34146488-34146489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573927359	chr22:34146496-34146497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542520668	chr22:34146540-34146541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112721316	chr22:34146543-34146544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11285128	chr22:34146569-34146570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531424436	chr22:34146575-34146576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs62225409	chr22:34146582-34146583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146187955	chr22:34146647-34146648	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs185754502	chr22:34146676-34146677	Weak transcription Enhancers	lncRNA	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
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2501 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34111200-34146200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr22:34123200-34152000	Weak transcription	Aorta	Aorta
3	chr22:34124800-34171000	Weak transcription	Ovary	ovary
4	chr22:34126200-34176200	Weak transcription	Spleen	Spleen
5	chr22:34131000-34154200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr22:34133800-34147600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr22:34134400-34164800	Weak transcription	Brain Anterior Caudate	brain
8	chr22:34136200-34148600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr22:34136200-34152800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr22:34136200-34152800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr22:34136400-34152600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr22:34136800-34152600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr22:34137200-34151000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr22:34137400-34152600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr22:34137600-34151000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr22:34137800-34152800	Weak transcription	Colon Smooth Muscle	Colon
17	chr22:34138000-34148600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr22:34138000-34152600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr22:34138000-34152800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr22:34138000-34160800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr22:34140800-34146000	Enhancers	Fetal Heart	heart
22	chr22:34140800-34149200	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr22:34140800-34152600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr22:34141600-34152600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr22:34141800-34149400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr22:34141800-34152400	Weak transcription	Fetal Stomach	stomach
27	chr22:34141800-34153200	Weak transcription	Psoas Muscle	Psoas
28	chr22:34142800-34152600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr22:34143400-34160000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr22:34143800-34149800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr22:34144400-34149400	Weak transcription	Fetal Muscle Leg	muscle
32	chr22:34144600-34145800	Weak transcription	Left Ventricle	heart
33	chr22:34144800-34145800	Weak transcription	Right Ventricle	heart
34	chr22:34145000-34146000	Weak transcription	Gastric	stomach
35	chr22:34145000-34148600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr22:34145000-34151000	Weak transcription	Fetal Intestine Large	intestine
37	chr22:34145000-34154000	Weak transcription	Primary B cells from peripheral blood	blood
38	chr22:34145200-34152600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr22:34145800-34146000	Enhancers	Right Ventricle	heart
40	chr22:34145800-34146400	Enhancers	Left Ventricle	heart
41	chr22:34146000-34146400	Enhancers	Gastric	stomach
42	chr22:34146000-34151400	Weak transcription	Fetal Heart	heart
43	chr22:34146000-34152600	Weak transcription	Right Ventricle	heart
44	chr22:34146200-34147600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr22:34146400-34152600	Weak transcription	Gastric	stomach
46	chr22:34146400-34152600	Weak transcription	Left Ventricle	heart
47	chr22:34147400-34158400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr22:34147400-34168600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr22:34147600-34148800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr22:34147600-34154600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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