Variant report

Variant	nsv881652
Chromosome Location	chr5:52323568-52385312
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:818)
CpG islands
(count:122)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:52327530-52328262	HepG2	liver:	n/a	n/a
2	ATF1	chr5:52325479-52325598	K562	blood:	n/a	n/a
3	ATF2	chr5:52336962-52337473	GM12878	blood:	n/a	n/a
4	ATF3	chr5:52327418-52327976	A549	lung:	n/a	n/a
5	ATF3	chr5:52327470-52328014	A549	lung:	n/a	n/a
6	BATF	chr5:52337121-52337510	GM12878	blood:	n/a	chr5:52337302-52337313
7	BATF	chr5:52337089-52337443	GM12878	blood:	n/a	chr5:52337302-52337313
8	BCL3	chr5:52328476-52328933	A549	lung:	n/a	n/a
9	BCL3	chr5:52327432-52328047	A549	lung:	n/a	n/a
10	BCL3	chr5:52328364-52328928	A549	lung:	n/a	n/a
11	BCLAF1	chr5:52337005-52337513	GM12878	blood:	n/a	chr5:52337129-52337138
12	BHLHE40	chr5:52337033-52337577	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:52332940-52333974	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr5:52325518-52325726	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:52341291-52341361	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:52323984-52324179	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:52327529-52327868	HepG2	liver:	n/a	chr5:52327691-52327702
18	CEBPB	chr5:52327457-52328012	A549	lung:	n/a	chr5:52327691-52327702
19	CEBPB	chr5:52327509-52327997	A549	lung:	n/a	chr5:52327691-52327702
20	CEBPB	chr5:52344146-52344352	IMR90	lung:	n/a	chr5:52344231-52344242
21	CEBPB	chr5:52327505-52327907	HepG2	liver:	n/a	chr5:52327691-52327702
22	CEBPB	chr5:52344106-52344390	Hela-S3	cervix:	n/a	chr5:52344231-52344242
23	CEBPB	chr5:52337641-52337832	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:52327512-52327865	HepG2	liver:	n/a	chr5:52327691-52327702
25	CEBPB	chr5:52363546-52363730	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:52341150-52341448	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:52327377-52328013	HCT-116	colon:	n/a	chr5:52327691-52327702
28	CEBPB	chr5:52333326-52333802	A549	lung:	n/a	chr5:52333644-52333656
29	CEBPB	chr5:52333302-52333724	MCF-7	breast:	n/a	chr5:52333644-52333656
30	CEBPB	chr5:52327475-52328041	IMR90	lung:	n/a	chr5:52327691-52327702
31	CEBPB	chr5:52344091-52344380	HepG2	liver:	n/a	chr5:52344231-52344242
32	CEBPB	chr5:52333142-52333796	IMR90	lung:	n/a	chr5:52333644-52333656
33	CEBPB	chr5:52327559-52327781	HepG2	liver:	n/a	chr5:52327691-52327702
34	CEBPB	chr5:52344124-52344350	A549	lung:	n/a	chr5:52344231-52344242
35	CEBPB	chr5:52385125-52385681	MCF-7	breast:	n/a	n/a
36	CEBPB	chr5:52332916-52333841	Hela-S3	cervix:	n/a	chr5:52333644-52333656
37	CEBPB	chr5:52334371-52334580	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:52327484-52328001	Hela-S3	cervix:	n/a	chr5:52327691-52327702
39	CEBPB	chr5:52327462-52327907	MCF-7	breast:	n/a	chr5:52327691-52327702
40	CEBPB	chr5:52327433-52327946	MCF-7	breast:	n/a	chr5:52327691-52327702
41	CEBPB	chr5:52385103-52385738	MCF-7	breast:	n/a	n/a
42	CEBPB	chr5:52333152-52333783	A549	lung:	n/a	chr5:52333644-52333656
43	CEBPB	chr5:52326741-52326923	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:52327299-52328176	HCT-116	colon:	n/a	chr5:52327691-52327702
45	CEBPB	chr5:52333085-52333939	HCT-116	colon:	n/a	chr5:52333644-52333656
46	CEBPB	chr5:52327257-52328145	A549	lung:	n/a	chr5:52327691-52327702
47	CEBPB	chr5:52327596-52327875	H1-hESC	embryonic stem cell:	n/a	chr5:52327691-52327702
48	CEBPB	chr5:52371996-52372190	HepG2	liver:	n/a	chr5:52372022-52372033
49	CHD2	chr5:52333153-52333740	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr5:52327496-52327949	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:52334107-52334157	NHDF-neo	bronchial:	n/a
2	chr5:52334107-52334157	HMEC	breast:	n/a
3	chr5:52327649-52327699	HEEpiC	esophagus:	n/a
4	chr5:52327649-52327699	HIPEpiC	eye:	n/a
5	chr5:52327649-52327699	HNPCEpiC	eye:	n/a
6	chr5:52334107-52334157	SK-N-SH_RA	brain:	n/a
7	chr5:52327649-52327699	HCT-116	colon:	n/a
8	chr5:52334107-52334157	Hela-S3	cervix:	n/a
9	chr5:52334107-52334157	HL-60	blood:	n/a
10	chr5:52334107-52334157	HNPCEpiC	eye:	n/a
11	chr5:52327649-52327699	ProgFib	skin:	n/a
12	chr5:52334107-52334157	AG09319	gingival:	n/a
13	chr5:52334107-52334157	AG04450	lung:	fetal
14	chr5:52327649-52327699	HCM	heart:	n/a
15	chr5:52327649-52327699	AoSMC	blood vessel:	n/a
16	chr5:52327649-52327699	K562	blood:	n/a
17	chr5:52334107-52334157	SAEC	small airway:	n/a
18	chr5:52334107-52334157	HEK293	kidney:	embryo
19	chr5:52334107-52334157	NH-A	brain:	n/a
20	chr5:52334107-52334157	HAEpiC	amniotic membrane:	n/a
21	chr5:52327649-52327699	HUVEC	blood vessel:	n/a
22	chr5:52334107-52334157	HCPEpiC	choroid plexus:	n/a
23	chr5:52334107-52334157	ProgFib	skin:	n/a
24	chr5:52334107-52334157	NB4	blood:	n/a
25	chr5:52334107-52334157	ovcar-3	ovarian:	n/a
26	chr5:52334107-52334157	ECC-1	luminal epithelium:	n/a
27	chr5:52327649-52327699	GM12891	blood:	n/a
28	chr5:52334107-52334157	AoSMC	blood vessel:	n/a
29	chr5:52334107-52334157	HRPEpiC	eye:	n/a
30	chr5:52327649-52327699	HRE	kidney:	n/a
31	chr5:52327649-52327699	AG04450	lung:	fetal
32	chr5:52327649-52327699	HRPEpiC	eye:	n/a
33	chr5:52327649-52327699	HMEC	breast:	n/a
34	chr5:52327649-52327699	PANC-1	pancreas:	n/a
35	chr5:52334107-52334157	U87	brain:	n/a
36	chr5:52334107-52334157	BE2_C	brain:	n/a
37	chr5:52334107-52334157	GM12878	blood:	n/a
38	chr5:52334107-52334157	AG09309	skin:	n/a
39	chr5:52334107-52334157	SK-N-MC	brain:	n/a
40	chr5:52327649-52327699	HepG2	liver:	n/a
41	chr5:52327649-52327699	NHDF-neo	bronchial:	n/a
42	chr5:52334107-52334157	AG10803	skin:	n/a
43	chr5:52327649-52327699	MCF-7	breast:	n/a
44	chr5:52327649-52327699	BE2_C	brain:	n/a
45	chr5:52334107-52334157	NT2-D1	testis:	n/a
46	chr5:52327649-52327699	Hepatocyte	liver:	n/a
47	chr5:52334107-52334157	LNCaP	prostate:	n/a
48	chr5:52327649-52327699	Hela-S3	cervix:	n/a
49	chr5:52327649-52327699	MCF10A-Er-Src	breast:	n/a
50	chr5:52334107-52334157	MCF-7	breast:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:52352312..52354080-chr5:52355424..52357750,2	K562	blood:
2	chr5:52382323..52385100-chr5:52387808..52389930,2	K562	blood:
3	chr5:52372459..52375173-chr5:52375877..52379453,3	MCF-7	breast:
4	chr5:52351776..52352321-chr9:91925750..91926479,2	MCF-7	breast:
5	chr5:52313064..52315275-chr5:52327348..52329688,2	MCF-7	breast:
6	chr5:52381586..52383200-chr5:52383742..52385269,2	MCF-7	breast:
7	chr17:62236129..62238534-chr5:52321834..52323811,2	MCF-7	breast:
8	chr5:52380023..52382035-chr5:52385112..52387338,2	K562	blood:
9	chr5:52319764..52321344-chr5:52327151..52329228,2	K562	blood:
10	chr5:52342580..52344559-chr5:52347867..52350544,2	K562	blood:
11	chr5:52342580..52344559-chr5:52347867..52350544,2	K562	blood:
12	chr5:52326404..52328383-chr5:52333260..52335027,2	MCF-7	breast:
13	chr5:52285122..52287993-chr5:52333837..52337640,3	MCF-7	breast:
14	chr5:52340133..52343071-chr5:52343982..52345648,2	K562	blood:
15	chr5:52376435..52379263-chr5:52381516..52385182,3	MCF-7	breast:
16	chr5:52381586..52383200-chr5:52383742..52385269,2	MCF-7	breast:
17	chr5:52352312..52354080-chr5:52355424..52357750,2	K562	blood:
18	chr5:52372459..52375173-chr5:52375877..52379453,3	MCF-7	breast:
19	chr5:52372832..52374615-chr5:52379311..52380988,2	K562	blood:
20	chr5:52376435..52379263-chr5:52381516..52385182,3	MCF-7	breast:
21	chr5:52285755..52287338-chr5:52380121..52382244,2	MCF-7	breast:
22	chr5:52384729..52387843-chr5:52404184..52407459,4	MCF-7	breast:
23	chr5:52326404..52328383-chr5:52333260..52335027,2	MCF-7	breast:
24	chr5:52318784..52321169-chr5:52323561..52325105,2	K562	blood:
25	chr5:52240942..52242706-chr5:52367816..52370164,2	MCF-7	breast:
26	chr5:52366890..52369025-chr5:52371234..52373244,2	K562	blood:
27	chr5:52340133..52343071-chr5:52343982..52345648,2	K562	blood:
28	chr5:52372832..52374615-chr5:52379311..52380988,2	K562	blood:
29	chr5:52284308..52287113-chr5:52321640..52324132,2	MCF-7	breast:
30	chr5:52366890..52369025-chr5:52371234..52373244,2	K562	blood:
31	chr5:52282372..52286768-chr5:52384365..52386788,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MOCS2-4	chr5:52384846-52385298	ENSG00000272123.1

No data

Variant related genes	Relation type
ENSG00000272123	TF binding region
ENSG00000272123	CpG island
ENSG00000272123	chromatin interactions
ENSG00000123975	chromatin interactions
ENSG00000247796	chromatin interactions
ENSG00000164172	chromatin interactions
ENSG00000249899	chromatin interactions
ENSG00000164171	chromatin interactions

Extended variants
information (count: 2333 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2333 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7705328	chr5:52323568-52323569	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149772545	chr5:52323580-52323581	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374676245	chr5:52323586-52323587	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs144703311	chr5:52323601-52323602	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148531690	chr5:52323620-52323621	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs544633617	chr5:52323649-52323650	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs13175177	chr5:52323674-52323675	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs13175183	chr5:52323680-52323681	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs9292004	chr5:52323720-52323721	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs1541689	chr5:52323757-52323758	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553810812	chr5:52323812-52323813	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs572185304	chr5:52323883-52323884	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371152982	chr5:52323910-52323911	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs146718788	chr5:52323929-52323930	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs528529087	chr5:52323946-52323947	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530561733	chr5:52324002-52324003	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs554905926	chr5:52324028-52324029	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs140351289	chr5:52324042-52324043	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543850932	chr5:52324053-52324054	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs565167411	chr5:52324116-52324117	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs577144415	chr5:52324125-52324126	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144130713	chr5:52324199-52324200	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs151011995	chr5:52324216-52324217	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530242132	chr5:52324249-52324250	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576886745	chr5:52324290-52324291	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140908860	chr5:52324292-52324293	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183846444	chr5:52324364-52324365	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531078307	chr5:52324418-52324419	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561174207	chr5:52324421-52324422	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528634501	chr5:52324427-52324428	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546898668	chr5:52324477-52324478	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545908105	chr5:52324482-52324483	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150086051	chr5:52324485-52324486	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374419292	chr5:52324493-52324494	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116044652	chr5:52324505-52324506	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532836906	chr5:52324518-52324519	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547182569	chr5:52324555-52324556	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565719993	chr5:52324577-52324578	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536470209	chr5:52324591-52324592	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554768019	chr5:52324653-52324654	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs117795422	chr5:52324659-52324660	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187040825	chr5:52324674-52324675	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74333369	chr5:52324698-52324699	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138409896	chr5:52324716-52324717	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558809810	chr5:52324721-52324722	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577206392	chr5:52324763-52324764	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541376439	chr5:52324775-52324776	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569218274	chr5:52324789-52324790	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559595772	chr5:52324847-52324848	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3212425	chr5:52324853-52324854	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52307000-52333800	Weak transcription	Gastric	stomach
2	chr5:52314200-52328600	Weak transcription	Lung	lung
3	chr5:52314200-52348000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:52314400-52326200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:52317200-52327200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:52317400-52326800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr5:52317600-52326800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr5:52317600-52333600	Weak transcription	Colonic Mucosa	Colon
9	chr5:52318400-52331800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:52318800-52327200	Genic enhancers	HMEC	breast
11	chr5:52319000-52325400	Enhancers	Brain Substantia Nigra	brain
12	chr5:52319200-52325400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr5:52319200-52326200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr5:52319200-52327600	Weak transcription	Fetal Intestine Large	intestine
15	chr5:52319600-52326600	Weak transcription	Small Intestine	intestine
16	chr5:52320600-52323600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr5:52320600-52326200	Weak transcription	Esophagus	oesophagus
18	chr5:52320600-52327400	Weak transcription	HSMM	muscle
19	chr5:52320600-52327600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:52321000-52323600	Weak transcription	NHDF-Ad	bronchial
21	chr5:52321000-52326600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr5:52321600-52323600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr5:52321600-52326800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr5:52321800-52326000	Weak transcription	Duodenum Mucosa	Duodenum
25	chr5:52321800-52326800	Weak transcription	Fetal Lung	lung
26	chr5:52322200-52326400	Genic enhancers	HepG2	liver
27	chr5:52322200-52333200	Weak transcription	Fetal Stomach	stomach
28	chr5:52322400-52324800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr5:52322600-52326400	Weak transcription	Fetal Kidney	kidney
30	chr5:52322800-52324000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:52323000-52324600	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr5:52323000-52324600	Enhancers	HUVEC	blood vessel
33	chr5:52323000-52324800	Enhancers	Brain Hippocampus Middle	brain
34	chr5:52323000-52326400	Genic enhancers	Hela-S3	cervix
35	chr5:52323000-52327000	Enhancers	A549	lung
36	chr5:52323000-52327200	Genic enhancers	NHEK	skin
37	chr5:52323200-52323800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr5:52323200-52324400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:52323200-52324400	Enhancers	Brain Angular Gyrus	brain
40	chr5:52323200-52324400	Enhancers	Brain Anterior Caudate	brain
41	chr5:52323200-52324800	Enhancers	Brain Cingulate Gyrus	brain
42	chr5:52323200-52324800	Enhancers	NH-A	brain
43	chr5:52323200-52326400	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:52323200-52326400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr5:52323200-52327000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr5:52323200-52329000	Enhancers	NHLF	lung
47	chr5:52323400-52323600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr5:52323400-52323600	Enhancers	Stomach Smooth Muscle	stomach
49	chr5:52323400-52323800	Enhancers	Pancreas	Pancrea
50	chr5:52323400-52324000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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