Variant report

Variant	nsv998425
Chromosome Location	chr4:9834666-9961280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:976)
CpG islands
(count:491)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9952887-9953127	K562	blood:	n/a	n/a
2	ATF1	chr4:9929162-9929613	K562	blood:	n/a	n/a
3	ATF1	chr4:9927280-9927595	K562	blood:	n/a	n/a
4	ATF1	chr4:9850013-9850273	K562	blood:	n/a	n/a
5	ATF3	chr4:9849946-9850297	K562	blood:	n/a	n/a
6	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr4:9851148-9851550	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:9851100-9851523	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:9872224-9872359	K562	blood:	n/a	n/a
10	BHLHE40	chr4:9867363-9867483	K562	blood:	n/a	n/a
11	BHLHE40	chr4:9920641-9920828	K562	blood:	n/a	n/a
12	BHLHE40	chr4:9851061-9851588	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:9882590-9882646	K562	blood:	n/a	n/a
14	BHLHE40	chr4:9937928-9938023	K562	blood:	n/a	n/a
15	BRCA1	chr4:9871086-9871272	GM12878	blood:	n/a	n/a
16	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
17	CCNT2	chr4:9937760-9938130	K562	blood:	n/a	n/a
18	CEBPB	chr4:9954135-9954305	HepG2	liver:	n/a	chr4:9954213-9954224
19	CEBPB	chr4:9876089-9876404	IMR90	lung:	n/a	chr4:9876241-9876252
20	CEBPB	chr4:9867161-9867312	HepG2	liver:	n/a	chr4:9867238-9867249
21	CEBPB	chr4:9954171-9954281	K562	blood:	n/a	chr4:9954213-9954224
22	CEBPB	chr4:9927304-9927536	K562	blood:	n/a	n/a
23	CEBPB	chr4:9954030-9954437	MCF-7	breast:	n/a	chr4:9954213-9954224
24	CEBPB	chr4:9954053-9954383	H1-hESC	embryonic stem cell:	n/a	chr4:9954213-9954224
25	CEBPB	chr4:9849949-9850302	HepG2	liver:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
26	CEBPB	chr4:9888675-9888963	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:9900230-9900797	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:9954068-9954391	HepG2	liver:	n/a	chr4:9954213-9954224
29	CEBPB	chr4:9954045-9954390	K562	blood:	n/a	chr4:9954213-9954224
30	CEBPB	chr4:9849824-9850326	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
31	CEBPB	chr4:9849998-9850279	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
32	CEBPB	chr4:9900393-9900739	MCF-7	breast:	n/a	n/a
33	CEBPB	chr4:9954066-9954414	HepG2	liver:	n/a	chr4:9954213-9954224
34	CEBPB	chr4:9849980-9850299	H1-hESC	embryonic stem cell:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
35	CEBPB	chr4:9849913-9850318	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
36	CEBPB	chr4:9927280-9927588	K562	blood:	n/a	n/a
37	CEBPB	chr4:9849900-9850296	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
38	CEBPB	chr4:9876209-9876280	K562	blood:	n/a	chr4:9876241-9876252
39	CEBPB	chr4:9915458-9915692	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr4:9895337-9895676	K562	blood:	n/a	n/a
41	CEBPB	chr4:9900383-9900669	K562	blood:	n/a	n/a
42	CEBPB	chr4:9895305-9895547	K562	blood:	n/a	n/a
43	CEBPB	chr4:9954093-9954373	A549	lung:	n/a	chr4:9954213-9954224
44	CEBPB	chr4:9876127-9876348	HepG2	liver:	n/a	chr4:9876241-9876252
45	CEBPB	chr4:9954044-9954358	K562	blood:	n/a	chr4:9954213-9954224
46	CEBPB	chr4:9849869-9850308	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
47	CEBPB	chr4:9849953-9850289	Hela-S3	cervix:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
48	CEBPB	chr4:9849993-9850301	A549	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
49	CEBPB	chr4:9849994-9850220	MCF-7	breast:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
50	CEBPB	chr4:9849942-9850300	IMR90	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9937674-9937724	GM19239	blood:	n/a
2	chr4:9884128-9884178	Hepatocyte	liver:	n/a
3	chr4:9892887-9892937	ovcar-3	ovarian:	n/a
4	chr4:9937674-9937724	GM19239	blood:	n/a
5	chr4:9884128-9884178	Hepatocyte	liver:	n/a
6	chr4:9892887-9892937	ovcar-3	ovarian:	n/a
7	chr4:9884128-9884178	AG09319	gingival:	n/a
8	chr4:9884128-9884178	ProgFib	skin:	n/a
9	chr4:9884128-9884178	HL-60	blood:	n/a
10	chr4:9940566-9940616	HL-60	blood:	n/a
11	chr4:9884128-9884178	GM12892	blood:	n/a
12	chr4:9892887-9892937	AG09319	gingival:	n/a
13	chr4:9884128-9884178	HRCEpiC	kidney:	n/a
14	chr4:9940566-9940616	AG04450	lung:	fetal
15	chr4:9950643-9950693	ECC-1	luminal epithelium:	n/a
16	chr4:9922462-9922512	AG10803	skin:	n/a
17	chr4:9892887-9892937	HRCEpiC	kidney:	n/a
18	chr4:9892887-9892937	HepG2	liver:	n/a
19	chr4:9926439-9926489	NHDF-neo	bronchial:	n/a
20	chr4:9892887-9892937	BJ	skin:	n/a
21	chr4:9950643-9950693	NHDF-neo	bronchial:	n/a
22	chr4:9940566-9940616	SAEC	small airway:	n/a
23	chr4:9940566-9940616	Caco-2	colon:	n/a
24	chr4:9950643-9950693	HAEpiC	amniotic membrane:	n/a
25	chr4:9937674-9937724	HRPEpiC	eye:	n/a
26	chr4:9892887-9892937	RPTEC	kidney:	n/a
27	chr4:9950643-9950693	PFSK-1	brain:	n/a
28	chr4:9950643-9950693	Jurkat	blood:	n/a
29	chr4:9884128-9884178	HUVEC	blood vessel:	n/a
30	chr4:9937674-9937724	HMEC	breast:	n/a
31	chr4:9940566-9940616	HRE	kidney:	n/a
32	chr4:9950643-9950693	HRPEpiC	eye:	n/a
33	chr4:9922462-9922512	HEK293	kidney:	embryo
34	chr4:9884128-9884178	HCM	heart:	n/a
35	chr4:9922462-9922512	NHDF-neo	bronchial:	n/a
36	chr4:9926439-9926489	HUVEC	blood vessel:	n/a
37	chr4:9917839-9917889	HNPCEpiC	eye:	n/a
38	chr4:9940566-9940616	HEEpiC	esophagus:	n/a
39	chr4:9926439-9926489	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:9922462-9922512	NB4	blood:	n/a
41	chr4:9917839-9917889	AG04449	skin:	fetal
42	chr4:9940566-9940616	NT2-D1	testis:	n/a
43	chr4:9892887-9892937	AoSMC	blood vessel:	n/a
44	chr4:9926439-9926489	K562	blood:	n/a
45	chr4:9922462-9922512	AG04450	lung:	fetal
46	chr4:9937674-9937724	GM12892	blood:	n/a
47	chr4:9940566-9940616	HRPEpiC	eye:	n/a
48	chr4:9884128-9884178	HCT-116	colon:	n/a
49	chr4:9892887-9892937	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:9892887-9892937	CMK	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
2	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
3	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
4	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
5	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
6	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
7	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
8	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
9	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
10	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
11	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
12	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
13	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
14	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
15	chr4:9929005..9929948-chr4:10015148..10015863,2	MCF-7	breast:
16	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
17	chr4:9920609..9921128-chr4:10020066..10020974,2	K562	blood:
18	chr4:9898528..9900449-chr4:10019179..10021130,2	MCF-7	breast:
19	chr4:9918331..9921142-chr4:10116868..10118418,2	MCF-7	breast:
20	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
21	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
22	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
23	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-1	chr4:9925400-9925770	ENSG00000249219.1
2	lnc-WDR1-12	chr4:9870401-9871383	NONHSAT095146
3	lnc-WDR1-12	chr4:9873428-9874487	NONHSAT095146
4	lnc-DRD5-1	chr4:9924438-9924574	ENSG00000249219.1

No data

Variant related genes	Relation type
ENSG00000249219	TF binding region
SLC2A9	TF binding region
ENSG00000249219	CpG island
SLC2A9	CpG island
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000109667	chromatin interactions

Extended variants
information (count: 5701 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5701 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112704137	chr4:9834673-9834674	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147774796	chr4:9834685-9834686	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534945193	chr4:9834693-9834694	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571231244	chr4:9834698-9834699	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532253907	chr4:9834720-9834721	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535785563	chr4:9834735-9834736	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367988499	chr4:9834760-9834761	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578095370	chr4:9834764-9834765	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569041704	chr4:9834791-9834792	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs16889260	chr4:9834896-9834897	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs188762362	chr4:9834939-9834940	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141183856	chr4:9834940-9834941	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541420499	chr4:9834958-9834959	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193194588	chr4:9834962-9834963	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149904665	chr4:9834963-9834964	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73804734	chr4:9834978-9834979	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs567763516	chr4:9834995-9834996	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs16889264	chr4:9834999-9835000	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs531139128	chr4:9835017-9835018	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184988464	chr4:9835021-9835022	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563856474	chr4:9835059-9835060	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528208843	chr4:9835082-9835083	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546182762	chr4:9835106-9835107	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143779704	chr4:9835128-9835129	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529132969	chr4:9835159-9835160	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550852514	chr4:9835176-9835177	Strong transcription ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568930300	chr4:9835240-9835241	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539634700	chr4:9835265-9835266	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563765921	chr4:9835310-9835311	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570936429	chr4:9835331-9835332	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114919407	chr4:9835352-9835353	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138463521	chr4:9835366-9835367	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs80146409	chr4:9835387-9835388	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367792492	chr4:9835393-9835394	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535728453	chr4:9835403-9835404	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141443035	chr4:9835454-9835455	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575717050	chr4:9835462-9835463	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10012880	chr4:9835480-9835481	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537832354	chr4:9835484-9835485	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs62295675	chr4:9835500-9835501	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113181369	chr4:9835517-9835518	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371115525	chr4:9835545-9835546	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375470599	chr4:9835550-9835551	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138811051	chr4:9835552-9835553	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188350953	chr4:9835554-9835555	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9996799	chr4:9835563-9835564	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs201547426	chr4:9835564-9835565	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs16889270	chr4:9835566-9835567	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs58782826	chr4:9835567-9835568	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562785118	chr4:9835604-9835605	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	17142309	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Obesity	21131291	CNVD
Schizophrenia	23813976	CNVD
Hepatocellular carcinoma	22267523	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:911 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9820200-9842600	Weak transcription	HMEC	breast
2	chr4:9823800-9836400	Weak transcription	Left Ventricle	heart
3	chr4:9825800-9835000	Weak transcription	Aorta	Aorta
4	chr4:9826400-9837600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:9829800-9839000	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr4:9830600-9836600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:9831600-9840600	Weak transcription	Pancreas	Pancrea
8	chr4:9832000-9837200	Strong transcription	HepG2	liver
9	chr4:9832200-9835000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr4:9832200-9839600	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr4:9832400-9835000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr4:9832400-9836400	Strong transcription	Liver	Liver
13	chr4:9832400-9836600	Strong transcription	Fetal Intestine Large	intestine
14	chr4:9832600-9836400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:9833200-9835800	Strong transcription	Fetal Intestine Small	intestine
16	chr4:9833400-9836400	Weak transcription	Lung	lung
17	chr4:9833600-9834800	Weak transcription	Right Atrium	heart
18	chr4:9833600-9835000	Weak transcription	Duodenum Mucosa	Duodenum
19	chr4:9833600-9840200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr4:9833800-9835800	Enhancers	Thymus	Thymus
21	chr4:9834000-9835000	Weak transcription	Esophagus	oesophagus
22	chr4:9834400-9835600	Strong transcription	NHEK	skin
23	chr4:9834800-9835600	Enhancers	Right Atrium	heart
24	chr4:9835000-9835200	ZNF genes & repeats	Aorta	Aorta
25	chr4:9835000-9835400	Strong transcription	Duodenum Smooth Muscle	Duodenum
26	chr4:9835000-9835400	Strong transcription	Esophagus	oesophagus
27	chr4:9835000-9835800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr4:9835000-9836200	Strong transcription	Duodenum Mucosa	Duodenum
29	chr4:9835000-9838400	Weak transcription	Spleen	Spleen
30	chr4:9835200-9838200	Weak transcription	Aorta	Aorta
31	chr4:9835400-9836800	Weak transcription	Esophagus	oesophagus
32	chr4:9835400-9838200	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr4:9835600-9840600	Weak transcription	NHEK	skin
34	chr4:9835800-9838000	Weak transcription	Fetal Intestine Small	intestine
35	chr4:9835800-9839200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr4:9836200-9837000	Enhancers	Fetal Kidney	kidney
37	chr4:9836200-9839200	Weak transcription	Duodenum Mucosa	Duodenum
38	chr4:9836400-9838000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:9836400-9838400	Weak transcription	Liver	Liver
40	chr4:9836600-9838400	Weak transcription	Fetal Intestine Large	intestine
41	chr4:9836600-9842600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:9836800-9837200	Enhancers	Esophagus	oesophagus
43	chr4:9837000-9837200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr4:9837200-9842400	Weak transcription	HepG2	liver
45	chr4:9837600-9838400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:9838000-9838600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:9838000-9838800	Strong transcription	Fetal Intestine Small	intestine
48	chr4:9838200-9838400	ZNF genes & repeats	Aorta	Aorta
49	chr4:9838400-9844800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:9838600-9842600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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