Variant report

Variant	nsv878686
Chromosome Location	chr4:9893403-10008305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1359)
CpG islands
(count:549)
Chromatin interactive
region (count:24)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1359 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10007887-10008235	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:10004013-10004296	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:9965207-9965232	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:9952887-9953127	K562	blood:	n/a	n/a
5	ARID3A	chr4:9998163-9998719	HepG2	liver:	n/a	n/a
6	ATF1	chr4:9929162-9929613	K562	blood:	n/a	n/a
7	ATF1	chr4:9927280-9927595	K562	blood:	n/a	n/a
8	ATF2	chr4:9991905-9992354	GM12878	blood:	n/a	n/a
9	ATF2	chr4:10007760-10008278	GM12878	blood:	n/a	n/a
10	ATF2	chr4:10007851-10008196	GM12878	blood:	n/a	n/a
11	ATF2	chr4:10005306-10005725	GM12878	blood:	n/a	n/a
12	ATF2	chr4:10001424-10002312	GM12878	blood:	n/a	n/a
13	ATF2	chr4:9972118-9972587	GM12878	blood:	n/a	n/a
14	ATF2	chr4:10001436-10002278	GM12878	blood:	n/a	n/a
15	ATF3	chr4:10003452-10003631	K562	blood:	n/a	n/a
16	BATF	chr4:10001742-10002251	GM12878	blood:	n/a	n/a
17	BATF	chr4:9972302-9972703	GM12878	blood:	n/a	n/a
18	BATF	chr4:10005411-10005658	GM12878	blood:	n/a	chr4:10005512-10005523
19	BCL11A	chr4:9972269-9972776	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:9972312-9972693	GM12878	blood:	n/a	n/a
21	BCL3	chr4:10005262-10005711	GM12878	blood:	n/a	n/a
22	BCL3	chr4:9989936-9990316	GM12878	blood:	n/a	n/a
23	BCL3	chr4:9991620-9991908	GM12878	blood:	n/a	n/a
24	BCL3	chr4:10007752-10008155	GM12878	blood:	n/a	n/a
25	BCL3	chr4:9989903-9990331	GM12878	blood:	n/a	n/a
26	BCL3	chr4:9991562-9991944	GM12878	blood:	n/a	n/a
27	BCLAF1	chr4:9972208-9972590	GM12878	blood:	n/a	n/a
28	BCLAF1	chr4:10007701-10008311	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:10007886-10008835	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:10003903-10004201	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:9983862-9984078	K562	blood:	n/a	n/a
32	BHLHE40	chr4:9920641-9920828	K562	blood:	n/a	n/a
33	BHLHE40	chr4:9962047-9962396	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:9937928-9938023	K562	blood:	n/a	n/a
35	BHLHE40	chr4:10007812-10009749	GM12878	blood:	n/a	n/a
36	BHLHE40	chr4:9972158-9972605	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:9964308-9964572	GM12878	blood:	n/a	n/a
38	BRCA1	chr4:9987308-9987348	GM12878	blood:	n/a	n/a
39	BRCA1	chr4:10008036-10008235	HepG2	liver:	n/a	n/a
40	CCNT2	chr4:9937760-9938130	K562	blood:	n/a	n/a
41	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
42	CEBPB	chr4:9954137-9954295	HepG2	liver:	n/a	chr4:9954213-9954224
43	CEBPB	chr4:9927280-9927588	K562	blood:	n/a	n/a
44	CEBPB	chr4:10007707-10008323	A549	lung:	n/a	n/a
45	CEBPB	chr4:10007846-10008230	A549	lung:	n/a	n/a
46	CEBPB	chr4:9954030-9954437	MCF-7	breast:	n/a	chr4:9954213-9954224
47	CEBPB	chr4:10007842-10008822	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:9964598-9964892	HepG2	liver:	n/a	chr4:9964756-9964767
49	CEBPB	chr4:10007852-10008196	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:9954135-9954305	HepG2	liver:	n/a	chr4:9954213-9954224

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9990048-9990098	HAEpiC	amniotic membrane:	n/a
2	chr4:9940566-9940616	RPTEC	kidney:	n/a
3	chr4:9922462-9922512	HAEpiC	amniotic membrane:	n/a
4	chr4:9950643-9950693	AG09319	gingival:	n/a
5	chr4:9950643-9950693	SKMC	muscle:	n/a
6	chr4:9990048-9990098	PFSK-1	brain:	n/a
7	chr4:9990048-9990098	SK-N-MC	brain:	n/a
8	chr4:9937674-9937724	AoSMC	blood vessel:	n/a
9	chr4:9937674-9937724	SKMC	muscle:	n/a
10	chr4:9926439-9926489	HIPEpiC	eye:	n/a
11	chr4:9917839-9917889	SK-N-MC	brain:	n/a
12	chr4:9990048-9990098	PrEC	prostate:	n/a
13	chr4:9950643-9950693	K562	blood:	n/a
14	chr4:9940566-9940616	HCM	heart:	n/a
15	chr4:9998017-9998067	HL-60	blood:	n/a
16	chr4:9950643-9950693	AG04450	lung:	fetal
17	chr4:9981202-9981252	HEK293	kidney:	embryo
18	chr4:9990048-9990098	GM19239	blood:	n/a
19	chr4:9926439-9926489	HCM	heart:	n/a
20	chr4:9950643-9950693	AG09309	skin:	n/a
21	chr4:9922462-9922512	T-47D	breast:	n/a
22	chr4:9998017-9998067	HEEpiC	esophagus:	n/a
23	chr4:9937674-9937724	NT2-D1	testis:	n/a
24	chr4:9950643-9950693	BE2_C	brain:	n/a
25	chr4:9950643-9950693	IMR90	lung:	fetal
26	chr4:9998017-9998067	NH-A	brain:	n/a
27	chr4:9917839-9917889	GM19239	blood:	n/a
28	chr4:9998017-9998067	Caco-2	colon:	n/a
29	chr4:9990048-9990098	HCT-116	colon:	n/a
30	chr4:9990048-9990098	NHBE	bronchial:	n/a
31	chr4:9917839-9917889	PrEC	prostate:	n/a
32	chr4:9937674-9937724	AG10803	skin:	n/a
33	chr4:9922462-9922512	NT2-D1	testis:	n/a
34	chr4:9917839-9917889	GM06990	blood:	n/a
35	chr4:9950643-9950693	NT2-D1	testis:	n/a
36	chr4:9981202-9981252	HL-60	blood:	n/a
37	chr4:9981202-9981252	NHBE	bronchial:	n/a
38	chr4:9922462-9922512	HL-60	blood:	n/a
39	chr4:9917839-9917889	AG10803	skin:	n/a
40	chr4:9950643-9950693	HRPEpiC	eye:	n/a
41	chr4:9917839-9917889	AG09319	gingival:	n/a
42	chr4:9998017-9998067	ovcar-3	ovarian:	n/a
43	chr4:9922462-9922512	PFSK-1	brain:	n/a
44	chr4:9981202-9981252	HEEpiC	esophagus:	n/a
45	chr4:9998017-9998067	HCM	heart:	n/a
46	chr4:9926439-9926489	LNCaP	prostate:	n/a
47	chr4:9940566-9940616	SAEC	small airway:	n/a
48	chr4:9950643-9950693	RPTEC	kidney:	n/a
49	chr4:9950643-9950693	Hepatocyte	liver:	n/a
50	chr4:9926439-9926489	Hela-S3	cervix:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
2	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
3	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
4	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
5	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
6	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
7	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
8	chr4:9999663..10002309-chr4:10003898..10006601,3	MCF-7	breast:
9	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
10	chr4:9918331..9921142-chr4:10116868..10118418,2	MCF-7	breast:
11	chr4:9999925..10002392-chr4:10005670..10008448,2	K562	blood:
12	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
13	chr4:9761130..9763005-chr4:9988480..9990175,2	K562	blood:
14	chr4:9898528..9900449-chr4:10019179..10021130,2	MCF-7	breast:
15	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
16	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
17	chr4:10003454..10005588-chr4:10009688..10011673,2	MCF-7	breast:
18	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
19	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
20	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
21	chr4:9929005..9929948-chr4:10015148..10015863,2	MCF-7	breast:
22	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
23	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
24	chr4:9920609..9921128-chr4:10020066..10020974,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-1	chr4:9925400-9925770	ENSG00000249219.1
2	lnc-DRD5-1	chr4:9924438-9924574	ENSG00000249219.1
3	lnc-DRD5-2	chr4:10008106-10008316	ENSG00000250413.1

No data

Variant related genes	Relation type
ENSG00000250413	TF binding region
ENSG00000249219	TF binding region
SLC2A9	TF binding region
ENSG00000250413	CpG island
ENSG00000249219	CpG island
SLC2A9	CpG island
ENSG00000250413	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000109667	chromatin interactions

Extended variants
information (count: 5160 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5160 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12644047	chr4:9893403-9893404	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542154354	chr4:9893408-9893409	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs563449474	chr4:9893414-9893415	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs34588837	chr4:9893433-9893434	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs148973683	chr4:9893468-9893469	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs184018190	chr4:9893469-9893470	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs189373655	chr4:9893470-9893471	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs551706537	chr4:9893497-9893498	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs143772489	chr4:9893498-9893499	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs7688167	chr4:9893506-9893507	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs547354753	chr4:9893509-9893510	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539419661	chr4:9893540-9893541	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs151104857	chr4:9893570-9893571	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs7669444	chr4:9893577-9893578	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548649614	chr4:9893589-9893590	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs570219920	chr4:9893594-9893595	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs537279539	chr4:9893633-9893634	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs376810873	chr4:9893674-9893675	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs141099164	chr4:9893721-9893722	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs375681148	chr4:9893741-9893742	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs145187844	chr4:9893744-9893745	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs368912184	chr4:9893784-9893785	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs567782518	chr4:9893794-9893795	Enhancers Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs542140481	chr4:9893801-9893802	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs138807148	chr4:9893810-9893811	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs372668184	chr4:9893814-9893815	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs575375247	chr4:9893815-9893816	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs367962733	chr4:9893819-9893820	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs180981171	chr4:9893826-9893827	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs12108499	chr4:9893849-9893850	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs184176151	chr4:9893904-9893905	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs371781357	chr4:9893911-9893912	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs559320220	chr4:9893930-9893931	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs141987055	chr4:9893935-9893936	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs542029091	chr4:9893940-9893941	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs145680108	chr4:9893969-9893970	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs189406737	chr4:9893974-9893975	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs112484524	chr4:9893976-9893977	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs186435048	chr4:9893981-9893982	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs571065046	chr4:9893983-9893984	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556096518	chr4:9893992-9893993	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs534657286	chr4:9894084-9894085	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs938561	chr4:9894094-9894095	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs190802285	chr4:9894143-9894144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181473996	chr4:9894225-9894226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556938509	chr4:9894235-9894236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575432907	chr4:9894248-9894249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186568231	chr4:9894260-9894261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117315041	chr4:9894261-9894262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191071035	chr4:9894278-9894279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1232 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9879200-9894800	Strong transcription	HepG2	liver
2	chr4:9879200-9894800	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr4:9879800-9894000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
4	chr4:9880200-9894600	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr4:9881000-9894200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:9882600-9903600	Weak transcription	Fetal Intestine Large	intestine
7	chr4:9885200-9893800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:9888800-9905800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr4:9889000-9906200	Weak transcription	Liver	Liver
10	chr4:9890600-9905600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr4:9890800-9893800	Weak transcription	Lung	lung
12	chr4:9891000-9895000	Weak transcription	Right Atrium	heart
13	chr4:9892200-9903600	Weak transcription	Fetal Intestine Small	intestine
14	chr4:9892800-9893800	Weak transcription	Spleen	Spleen
15	chr4:9892800-9903600	Weak transcription	NHEK	skin
16	chr4:9893400-9897600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:9893400-9900200	Weak transcription	HMEC	breast
18	chr4:9893600-9893800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:9893800-9894000	Enhancers	Lung	lung
20	chr4:9893800-9894200	Enhancers	Spleen	Spleen
21	chr4:9893800-9899400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:9894000-9897000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr4:9894000-9917800	Weak transcription	Lung	lung
24	chr4:9894200-9897600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:9894600-9896200	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr4:9894800-9895600	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr4:9894800-9903400	Weak transcription	HepG2	liver
28	chr4:9895000-9895800	Enhancers	Right Atrium	heart
29	chr4:9895400-9895800	Enhancers	Fetal Muscle Leg	muscle
30	chr4:9895600-9896800	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr4:9895800-9896000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:9895800-9896800	Weak transcription	Fetal Muscle Leg	muscle
33	chr4:9895800-9906800	Weak transcription	Right Atrium	heart
34	chr4:9896200-9897400	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr4:9896400-9896600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:9896800-9897000	Enhancers	Fetal Muscle Leg	muscle
37	chr4:9896800-9897000	Enhancers	GM12878-XiMat	blood
38	chr4:9896800-9898000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr4:9897000-9924600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr4:9897400-9898400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr4:9897600-9898800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:9897600-9899800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:9898000-9902000	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr4:9898400-9899800	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr4:9898800-9899400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:9899400-9902200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:9899400-9902400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:9899600-9899800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr4:9899600-9899800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:9899800-9900400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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