Variant report

Variant	nsv1004311
Chromosome Location	chr4:9825814-9978414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1147)
CpG islands
(count:488)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1147 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9965207-9965232	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:9952887-9953127	K562	blood:	n/a	n/a
3	ATF1	chr4:9929162-9929613	K562	blood:	n/a	n/a
4	ATF1	chr4:9927280-9927595	K562	blood:	n/a	n/a
5	ATF1	chr4:9850013-9850273	K562	blood:	n/a	n/a
6	ATF2	chr4:9972118-9972587	GM12878	blood:	n/a	n/a
7	ATF3	chr4:9849946-9850297	K562	blood:	n/a	n/a
8	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr4:9972302-9972703	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:9972269-9972776	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:9851100-9851523	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:9972312-9972693	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:9851148-9851550	GM12878	blood:	n/a	n/a
14	BCL3	chr4:9826836-9827129	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:9972208-9972590	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:9972158-9972605	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:9937928-9938023	K562	blood:	n/a	n/a
18	BHLHE40	chr4:9964308-9964572	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:9867363-9867483	K562	blood:	n/a	n/a
20	BHLHE40	chr4:9882590-9882646	K562	blood:	n/a	n/a
21	BHLHE40	chr4:9920641-9920828	K562	blood:	n/a	n/a
22	BHLHE40	chr4:9872224-9872359	K562	blood:	n/a	n/a
23	BHLHE40	chr4:9962047-9962396	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:9851061-9851588	GM12878	blood:	n/a	n/a
25	BRCA1	chr4:9829608-9829617	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr4:9871086-9871272	GM12878	blood:	n/a	n/a
27	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
28	CCNT2	chr4:9937760-9938130	K562	blood:	n/a	n/a
29	CEBPB	chr4:9895337-9895676	K562	blood:	n/a	n/a
30	CEBPB	chr4:9849998-9850279	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
31	CEBPB	chr4:9900375-9900657	K562	blood:	n/a	n/a
32	CEBPB	chr4:9849900-9850296	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
33	CEBPB	chr4:9954030-9954437	MCF-7	breast:	n/a	chr4:9954213-9954224
34	CEBPB	chr4:9964598-9964892	HepG2	liver:	n/a	chr4:9964756-9964767
35	CEBPB	chr4:9900383-9900669	K562	blood:	n/a	n/a
36	CEBPB	chr4:9849942-9850300	IMR90	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
37	CEBPB	chr4:9849949-9850302	HepG2	liver:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
38	CEBPB	chr4:9849824-9850326	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
39	CEBPB	chr4:9895305-9895547	K562	blood:	n/a	n/a
40	CEBPB	chr4:9849993-9850301	A549	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
41	CEBPB	chr4:9954045-9954390	K562	blood:	n/a	chr4:9954213-9954224
42	CEBPB	chr4:9876089-9876404	IMR90	lung:	n/a	chr4:9876241-9876252
43	CEBPB	chr4:9915458-9915692	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:9954068-9954391	HepG2	liver:	n/a	chr4:9954213-9954224
45	CEBPB	chr4:9888675-9888963	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:9954066-9954414	HepG2	liver:	n/a	chr4:9954213-9954224
47	CEBPB	chr4:9900230-9900797	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:9954137-9954295	HepG2	liver:	n/a	chr4:9954213-9954224
49	CEBPB	chr4:9867161-9867312	HepG2	liver:	n/a	chr4:9867238-9867249
50	CEBPB	chr4:9927304-9927536	K562	blood:	n/a	n/a

(count:488 , 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	HIPEpiC	eye:	n/a
2	chr4:9884128-9884178	GM06990	blood:	n/a
3	chr4:9884128-9884178	HCPEpiC	choroid plexus:	n/a
4	chr4:9917839-9917889	HL-60	blood:	n/a
5	chr4:9940566-9940616	NH-A	brain:	n/a
6	chr4:9950643-9950693	HCPEpiC	choroid plexus:	n/a
7	chr4:9917839-9917889	GM12878	blood:	n/a
8	chr4:9940566-9940616	Hepatocyte	liver:	n/a
9	chr4:9937674-9937724	Caco-2	colon:	n/a
10	chr4:9917839-9917889	SK-N-SH_RA	brain:	n/a
11	chr4:9922462-9922512	HCM	heart:	n/a
12	chr4:9950643-9950693	MCF-7	breast:	n/a
13	chr4:9940566-9940616	HCPEpiC	choroid plexus:	n/a
14	chr4:9884128-9884178	GM12892	blood:	n/a
15	chr4:9940566-9940616	HepG2	liver:	n/a
16	chr4:9940566-9940616	AG09319	gingival:	n/a
17	chr4:9884128-9884178	HEK293	kidney:	embryo
18	chr4:9926439-9926489	U87	brain:	n/a
19	chr4:9917839-9917889	HepG2	liver:	n/a
20	chr4:9937674-9937724	RPTEC	kidney:	n/a
21	chr4:9940566-9940616	CMK	blood:	n/a
22	chr4:9926439-9926489	BJ	skin:	n/a
23	chr4:9940566-9940616	PFSK-1	brain:	n/a
24	chr4:9926439-9926489	NH-A	brain:	n/a
25	chr4:9940566-9940616	K562	blood:	n/a
26	chr4:9940566-9940616	ECC-1	luminal epithelium:	n/a
27	chr4:9926439-9926489	NHBE	bronchial:	n/a
28	chr4:9884128-9884178	PrEC	prostate:	n/a
29	chr4:9950643-9950693	HRE	kidney:	n/a
30	chr4:9950643-9950693	HUVEC	blood vessel:	n/a
31	chr4:9892887-9892937	ProgFib	skin:	n/a
32	chr4:9922462-9922512	H1-hESC	embryonic stem cell:	embryo
33	chr4:9917839-9917889	AG10803	skin:	n/a
34	chr4:9884128-9884178	SK-N-MC	brain:	n/a
35	chr4:9937674-9937724	AG09309	skin:	n/a
36	chr4:9884128-9884178	HRPEpiC	eye:	n/a
37	chr4:9926439-9926489	LNCaP	prostate:	n/a
38	chr4:9892887-9892937	AoSMC	blood vessel:	n/a
39	chr4:9884128-9884178	LNCaP	prostate:	n/a
40	chr4:9922462-9922512	RPTEC	kidney:	n/a
41	chr4:9917839-9917889	Hela-S3	cervix:	n/a
42	chr4:9922462-9922512	BE2_C	brain:	n/a
43	chr4:9937674-9937724	HMEC	breast:	n/a
44	chr4:9950643-9950693	HCF	heart:	n/a
45	chr4:9937674-9937724	HRPEpiC	eye:	n/a
46	chr4:9922462-9922512	GM12892	blood:	n/a
47	chr4:9950643-9950693	A549	lung:	n/a
48	chr4:9884128-9884178	HNPCEpiC	eye:	n/a
49	chr4:9926439-9926489	HepG2	liver:	n/a
50	chr4:9950643-9950693	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
2	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
3	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
4	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
5	chr4:9929005..9929948-chr4:10015148..10015863,2	MCF-7	breast:
6	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
7	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
8	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
9	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
10	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
11	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
12	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
13	chr4:9898528..9900449-chr4:10019179..10021130,2	MCF-7	breast:
14	chr4:9918331..9921142-chr4:10116868..10118418,2	MCF-7	breast:
15	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
16	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
17	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
18	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
19	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
20	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
21	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
22	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
23	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
24	chr4:9827283..9829135-chr4:9829200..9831465,2	K562	blood:
25	chr4:9920609..9921128-chr4:10020066..10020974,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-12	chr4:9870401-9871383	NONHSAT095146
2	lnc-WDR1-12	chr4:9873428-9874487	NONHSAT095146
3	lnc-DRD5-1	chr4:9925400-9925770	ENSG00000249219.1
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
ENSG00000109667	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 6807 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6807 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1996335	chr4:9825814-9825815	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs60111228	chr4:9825823-9825824	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs57731161	chr4:9825847-9825848	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs557864622	chr4:9825858-9825859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147076438	chr4:9825889-9825890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs5856021	chr4:9825934-9825935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540527147	chr4:9825963-9825964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555641447	chr4:9826023-9826024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138475000	chr4:9826050-9826051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79095673	chr4:9826077-9826078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562777787	chr4:9826080-9826081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532844679	chr4:9826095-9826096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545138022	chr4:9826142-9826143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376775624	chr4:9826147-9826148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4697893	chr4:9826183-9826184	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184261910	chr4:9826235-9826236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548959845	chr4:9826266-9826267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190475537	chr4:9826328-9826329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531669495	chr4:9826337-9826338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114681969	chr4:9826374-9826375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147322267	chr4:9826396-9826397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148805490	chr4:9826407-9826408	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs56741911	chr4:9826492-9826493	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs566704010	chr4:9826499-9826500	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534217384	chr4:9826558-9826559	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555604613	chr4:9826572-9826573	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4697894	chr4:9826603-9826604	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182261938	chr4:9826628-9826629	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141401196	chr4:9826644-9826645	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116209794	chr4:9826681-9826682	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369684599	chr4:9826727-9826728	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117535295	chr4:9826729-9826730	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs6822889	chr4:9826757-9826758	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs529831000	chr4:9826795-9826796	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185506460	chr4:9826798-9826799	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1519092	chr4:9826801-9826802	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560895400	chr4:9826807-9826808	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531633698	chr4:9826816-9826817	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550140293	chr4:9826822-9826823	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565029105	chr4:9826845-9826846	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs60026409	chr4:9826847-9826848	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs4621429	chr4:9826870-9826871	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs189054362	chr4:9826917-9826918	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534069929	chr4:9826938-9826939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377469378	chr4:9826991-9826992	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567371985	chr4:9826992-9826993	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538142368	chr4:9826994-9826995	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115947204	chr4:9827033-9827034	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181552377	chr4:9827050-9827051	Strong transcription Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185623560	chr4:9827099-9827100	Strong transcription Enhancers Weak transcription Genic 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:1084 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9808200-9832000	Weak transcription	Duodenum Mucosa	Duodenum
2	chr4:9808800-9834400	Weak transcription	NHEK	skin
3	chr4:9810000-9830600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:9811000-9827000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:9813400-9826600	Weak transcription	HepG2	liver
6	chr4:9820200-9826400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:9820200-9842600	Weak transcription	HMEC	breast
8	chr4:9820400-9833400	Weak transcription	Esophagus	oesophagus
9	chr4:9821000-9832400	Weak transcription	Liver	Liver
10	chr4:9821400-9826800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:9821600-9833200	Weak transcription	Fetal Intestine Small	intestine
12	chr4:9822400-9828400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr4:9823800-9836400	Weak transcription	Left Ventricle	heart
14	chr4:9824000-9832400	Weak transcription	Fetal Intestine Large	intestine
15	chr4:9824400-9828400	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr4:9825800-9835000	Weak transcription	Aorta	Aorta
17	chr4:9826400-9826800	Enhancers	Primary T cells from cord blood	blood
18	chr4:9826400-9826800	Enhancers	GM12878-XiMat	blood
19	chr4:9826400-9827600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr4:9826400-9827600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:9826400-9827600	Enhancers	Fetal Thymus	thymus
22	chr4:9826400-9837600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:9826600-9827200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr4:9826600-9827400	Enhancers	Thymus	Thymus
25	chr4:9826600-9828600	Strong transcription	HepG2	liver
26	chr4:9826800-9827000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:9827000-9827400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:9827000-9827600	Enhancers	Primary hematopoietic stem cells	blood
29	chr4:9827000-9832400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr4:9827400-9827600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:9827600-9832600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:9828400-9829800	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr4:9828400-9829800	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr4:9828600-9829000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr4:9828600-9832000	Weak transcription	HepG2	liver
36	chr4:9829800-9830400	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr4:9829800-9839000	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr4:9830400-9832200	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr4:9830600-9836600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:9831600-9840600	Weak transcription	Pancreas	Pancrea
41	chr4:9832000-9833600	Strong transcription	Duodenum Mucosa	Duodenum
42	chr4:9832000-9837200	Strong transcription	HepG2	liver
43	chr4:9832200-9835000	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr4:9832200-9839600	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr4:9832400-9833600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
46	chr4:9832400-9835000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr4:9832400-9836400	Strong transcription	Liver	Liver
48	chr4:9832400-9836600	Strong transcription	Fetal Intestine Large	intestine
49	chr4:9832600-9836400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:9833200-9833400	ZNF genes & repeats	Lung	lung

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