Variant report

Variant	nsv536670
Chromosome Location	chr3:100354611-100451403
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1502)
CpG islands
(count:1161)
Chromatin interactive
region (count:74)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1502 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
3	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100428405-100428550	K562	blood:	n/a	n/a
6	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
7	ATF1	chr3:100427978-100428440	K562	blood:	n/a	n/a
8	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
9	ATF2	chr3:100429275-100429952	GM12878	blood:	n/a	n/a
10	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
11	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
12	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
13	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
15	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
16	BACH1	chr3:100428023-100428678	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr3:100429220-100429801	GM12878	blood:	n/a	n/a
18	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
19	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
20	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
21	BATF	chr3:100429333-100429812	GM12878	blood:	n/a	n/a
22	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
26	BCLAF1	chr3:100428169-100428667	GM12878	blood:	n/a	chr3:100428545-100428558 chr3:100428541-100428554 chr3:100428539-100428552
27	BCLAF1	chr3:100429350-100429879	GM12878	blood:	n/a	chr3:100429694-100429703 chr3:100429744-100429753 chr3:100429743-100429752
28	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
29	BHLHE40	chr3:100427970-100428628	HepG2	liver:	n/a	chr3:100428533-100428549
30	BHLHE40	chr3:100427985-100428525	K562	blood:	n/a	n/a
31	BHLHE40	chr3:100428011-100428266	A549	lung:	n/a	n/a
32	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:100428885-100428960	K562	blood:	n/a	n/a
34	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
35	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr3:100428290-100428586	HepG2	liver:	n/a	n/a
37	BRCA1	chr3:100447701-100447710	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr3:100429415-100429752	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
41	BRCA1	chr3:100428898-100429175	H1-hESC	embryonic stem cell:	n/a	n/a
42	CBX3	chr3:100415727-100416040	K562	blood:	n/a	n/a
43	CBX3	chr3:100427818-100428510	K562	blood:	n/a	n/a
44	CBX3	chr3:100429573-100429981	K562	blood:	n/a	n/a
45	CCNT2	chr3:100427839-100429006	K562	blood:	n/a	chr3:100428771-100428780 chr3:100428796-100428805
46	CEBPB	chr3:100381321-100381668	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:100420298-100420583	K562	blood:	n/a	n/a
48	CEBPB	chr3:100370097-100370487	IMR90	lung:	n/a	chr3:100370349-100370362
49	CEBPB	chr3:100447872-100448108	K562	blood:	n/a	n/a
50	CEBPB	chr3:100416737-100417099	HepG2	liver:	n/a	chr3:100416923-100416934

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100401270-100401320	SK-N-MC	brain:	n/a
2	chr3:100428005-100428055	HRE	kidney:	n/a
3	chr3:100401270-100401320	SK-N-MC	brain:	n/a
4	chr3:100428005-100428055	HRE	kidney:	n/a
5	chr3:100428147-100428197	Caco-2	colon:	n/a
6	chr3:100401270-100401320	PANC-1	pancreas:	n/a
7	chr3:100428398-100428448	HCF	heart:	n/a
8	chr3:100428398-100428448	HCPEpiC	choroid plexus:	n/a
9	chr3:100428398-100428448	AG10803	skin:	n/a
10	chr3:100427096-100427146	HRPEpiC	eye:	n/a
11	chr3:100428642-100428692	AG09319	gingival:	n/a
12	chr3:100428140-100428190	LNCaP	prostate:	n/a
13	chr3:100428642-100428692	PFSK-1	brain:	n/a
14	chr3:100428172-100428222	ovcar-3	ovarian:	n/a
15	chr3:100428070-100428120	AG04450	lung:	fetal
16	chr3:100427096-100427146	H1-hESC	embryonic stem cell:	embryo
17	chr3:100428147-100428197	GM06990	blood:	n/a
18	chr3:100428172-100428222	SK-N-SH	brain:	n/a
19	chr3:100428642-100428692	GM06990	blood:	n/a
20	chr3:100428869-100428919	U87	brain:	n/a
21	chr3:100437347-100437397	GM12892	blood:	n/a
22	chr3:100428140-100428190	GM12892	blood:	n/a
23	chr3:100428005-100428055	HCF	heart:	n/a
24	chr3:100430811-100430861	SK-N-MC	brain:	n/a
25	chr3:100424830-100424880	HRPEpiC	eye:	n/a
26	chr3:100428172-100428222	Caco-2	colon:	n/a
27	chr3:100401284-100401334	HNPCEpiC	eye:	n/a
28	chr3:100428642-100428692	HRCEpiC	kidney:	n/a
29	chr3:100424830-100424880	Hepatocyte	liver:	n/a
30	chr3:100428398-100428448	GM12878	blood:	n/a
31	chr3:100424830-100424880	Jurkat	blood:	n/a
32	chr3:100428033-100428083	HCF	heart:	n/a
33	chr3:100427096-100427146	PFSK-1	brain:	n/a
34	chr3:100428398-100428448	NHBE	bronchial:	n/a
35	chr3:100430811-100430861	ECC-1	luminal epithelium:	n/a
36	chr3:100428398-100428448	U87	brain:	n/a
37	chr3:100427096-100427146	HRE	kidney:	n/a
38	chr3:100428172-100428222	GM06990	blood:	n/a
39	chr3:100427096-100427146	HNPCEpiC	eye:	n/a
40	chr3:100428642-100428692	HEK293	kidney:	embryo
41	chr3:100427239-100427289	Caco-2	colon:	n/a
42	chr3:100428172-100428222	HCM	heart:	n/a
43	chr3:100437347-100437397	IMR90	lung:	fetal
44	chr3:100428869-100428919	HMEC	breast:	n/a
45	chr3:100401270-100401320	SK-N-SH_RA	brain:	n/a
46	chr3:100428070-100428120	PrEC	prostate:	n/a
47	chr3:100401284-100401334	ECC-1	luminal epithelium:	n/a
48	chr3:100430811-100430861	U87	brain:	n/a
49	chr3:100428642-100428692	SK-N-SH	brain:	n/a
50	chr3:100428033-100428083	PFSK-1	brain:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
2	chr1:151512640..151513443-chr3:100428519..100429048,2	Hela-S3	cervix:
3	chr3:100448313..100450197-chr3:100453971..100455531,2	K562	blood:
4	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
5	chr3:100427327..100429549-chr3:100443145..100445427,2	K562	blood:
6	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
7	chr3:100419966..100423130-chr3:100426813..100428964,3	K562	blood:
8	chr3:100434706..100436343-chr3:100445572..100447869,2	K562	blood:
9	chr3:100364940..100366707-chr3:100366782..100369483,3	K562	blood:
10	chr3:100428105..100429880-chr3:100429992..100431694,2	K562	blood:
11	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
12	chr18:3247419..3248282-chr3:100427656..100428171,2	Hela-S3	cervix:
13	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
14	chr3:100427539..100430990-chr3:100441684..100444095,3	MCF-7	breast:
15	chr3:100451065..100453351-chr3:100454518..100456261,2	K562	blood:
16	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
17	chr3:100426752..100429566-chr3:100442716..100444671,3	K562	blood:
18	chr3:100412000..100414603-chr3:100428096..100429901,2	K562	blood:
19	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
20	chr3:100425991..100429784-chr3:100429994..100431694,4	K562	blood:
21	chr3:100448286..100450291-chr3:100462074..100463952,2	MCF-7	breast:
22	chr12:56435446..56435990-chr3:100428103..100428866,2	Hela-S3	cervix:
23	chr3:99535346..99537040-chr3:100436340..100438429,2	K562	blood:
24	chr3:100434706..100436343-chr3:100445572..100447869,2	K562	blood:
25	chr3:100118924..100121912-chr3:100362623..100364573,2	K562	blood:
26	chr3:100427232..100427732-chr9:96215167..96215670,2	Hela-S3	cervix:
27	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
28	chr3:100437193..100438903-chr3:100441910..100444444,2	K562	blood:
29	chr3:100442764..100445441-chr3:100450170..100452232,2	K562	blood:
30	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
31	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
32	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
33	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
34	chr3:100363955..100366251-chr3:100430276..100432024,2	K562	blood:
35	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
36	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
37	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
38	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
39	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
40	chr3:100428339..100431099-chr3:100444238..100445960,2	MCF-7	breast:
41	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
42	chr2:67550820..67551820-chr3:100427957..100428561,3	HCT-116	colon:
43	chr3:100428169..100430169-chr3:100436770..100441506,6	MCF-7	breast:
44	chr3:100428095..100432338-chr3:100432996..100435628,5	K562	blood:
45	chr3:100441058..100442704-chr3:100448594..100450149,2	K562	blood:
46	chr3:100120411..100122999-chr3:100364924..100367578,2	K562	blood:
47	chr3:100444141..100445657-chr3:100447158..100448973,2	K562	blood:
48	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
49	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
50	chr3:100437193..100438903-chr3:100441910..100444444,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM45A-1	chr3:100354384-100354670	NONHSAT090874
2	lnc-TMEM45A-1	chr3:100356146-100356419	NONHSAT090874
3	lnc-ABI3BP-1	chr3:100383894-100384320	NONHSAT090876

No data

Variant related genes	Relation type
TFG	TF binding region
GPR128	TF binding region
ENSG00000252989	TF binding region
GMFBP1	TF binding region
TFG	CpG island
GPR128	CpG island
ENSG00000252989	CpG island
GMFBP1	CpG island
ENSG00000184220	chromatin interactions
ENSG00000236605	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000257449	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000100983	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000197728	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000199004	chromatin interactions

Extended variants
information (count: 3895 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3895 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199704593	chr3:100354612-100354613	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs190503505	chr3:100354621-100354622	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs142118691	chr3:100354622-100354623	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs374653172	chr3:100354623-100354624	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs561983833	chr3:100354624-100354625	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs150675938	chr3:100354633-100354634	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs543518317	chr3:100354656-100354657	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs368713866	chr3:100354658-100354659	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs1520652	chr3:100354683-100354684	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs201699644	chr3:100354689-100354690	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532138567	chr3:100354696-100354697	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573702880	chr3:100354698-100354699	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183117613	chr3:100354699-100354700	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79409266	chr3:100354713-100354714	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78754646	chr3:100354714-100354715	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529836893	chr3:100354757-100354758	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548009741	chr3:100354762-100354763	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569801502	chr3:100354794-100354795	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188782193	chr3:100354798-100354799	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150890123	chr3:100354830-100354831	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374526054	chr3:100354841-100354842	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368718743	chr3:100354848-100354849	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78186356	chr3:100354857-100354858	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535058316	chr3:100354962-100354963	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200607691	chr3:100354998-100354999	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191124653	chr3:100355063-100355064	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1520651	chr3:100355094-100355095	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs16842441	chr3:100355104-100355105	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs557552747	chr3:100355192-100355193	Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575814688	chr3:100355203-100355204	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543106450	chr3:100355243-100355244	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183434898	chr3:100355316-100355317	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113873188	chr3:100355317-100355318	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540672403	chr3:100355335-100355336	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78774300	chr3:100355338-100355339	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543961821	chr3:100355369-100355370	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556269945	chr3:100355388-100355389	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4928070	chr3:100355419-100355420	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs139697060	chr3:100355450-100355451	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs76065821	chr3:100355489-100355490	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs397792547	chr3:100355499-100355500	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs569464841	chr3:100355518-100355519	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560379817	chr3:100355526-100355527	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191286370	chr3:100355594-100355595	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558891628	chr3:100355662-100355663	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528173189	chr3:100355663-100355664	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541483944	chr3:100355687-100355688	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528000134	chr3:100355702-100355703	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184545918	chr3:100355715-100355716	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs187810367	chr3:100355838-100355839	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1942 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100352800-100354800	Enhancers	Fetal Intestine Small	intestine
2	chr3:100353800-100355200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr3:100353800-100356200	Enhancers	Fetal Intestine Large	intestine
4	chr3:100354000-100357800	Weak transcription	Fetal Brain Male	brain
5	chr3:100354400-100355200	Enhancers	HepG2	liver
6	chr3:100354400-100356800	Weak transcription	Pancreas	Pancrea
7	chr3:100354400-100359000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:100354400-100360000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr3:100354600-100355400	Flanking Active TSS	Liver	Liver
10	chr3:100354600-100355600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr3:100354600-100359600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:100354800-100355000	Enhancers	Small Intestine	intestine
13	chr3:100354800-100357600	Genic enhancers	Fetal Intestine Small	intestine
14	chr3:100355000-100359800	Weak transcription	Small Intestine	intestine
15	chr3:100355200-100357000	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr3:100355200-100359000	Weak transcription	HepG2	liver
17	chr3:100355400-100355800	Active TSS	Liver	Liver
18	chr3:100355600-100357600	Strong transcription	Duodenum Mucosa	Duodenum
19	chr3:100355800-100356400	Flanking Active TSS	Liver	Liver
20	chr3:100355800-100356600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:100356000-100356600	Bivalent Enhancer	NHDF-Ad	bronchial
22	chr3:100356200-100356600	Bivalent Enhancer	Osteobl	bone
23	chr3:100356200-100359200	Genic enhancers	Fetal Intestine Large	intestine
24	chr3:100356400-100356600	Transcr. at gene 5' and 3'	Liver	Liver
25	chr3:100356600-100357400	ZNF genes & repeats	Liver	Liver
26	chr3:100356800-100357200	ZNF genes & repeats	Pancreas	Pancrea
27	chr3:100357000-100359200	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr3:100357400-100358200	Weak transcription	Liver	Liver
29	chr3:100357600-100358400	Weak transcription	Duodenum Mucosa	Duodenum
30	chr3:100357600-100358400	Weak transcription	Fetal Intestine Small	intestine
31	chr3:100358200-100360400	Enhancers	Liver	Liver
32	chr3:100358400-100361200	Enhancers	Duodenum Mucosa	Duodenum
33	chr3:100358400-100362200	Enhancers	Fetal Intestine Small	intestine
34	chr3:100359000-100360000	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr3:100359000-100360400	Enhancers	HepG2	liver
36	chr3:100359200-100359600	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr3:100359200-100361600	Enhancers	Fetal Intestine Large	intestine
38	chr3:100359600-100360200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr3:100359600-100360400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr3:100359600-100362000	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr3:100359800-100360200	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr3:100359800-100361200	Enhancers	Small Intestine	intestine
43	chr3:100359800-100361600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr3:100360000-100360400	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr3:100360200-100360800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr3:100360200-100361000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr3:100360200-100361200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:100360200-100361600	Enhancers	Primary hematopoietic stem cells	blood
49	chr3:100360400-100360800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:100360400-100360800	Enhancers	HUVEC	blood vessel

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