Variant report

Variant	nsv308
Chromosome Location	chr11:46242287-46287542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2357)
CpG islands
(count:1466)
Chromatin interactive
region (count:207)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2357 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46269177-46269434	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:46274059-46274437	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:46270189-46271592	K562	blood:	n/a	n/a
4	ARID3A	chr11:46263935-46264104	K562	blood:	n/a	n/a
5	ARID3A	chr11:46278116-46278448	K562	blood:	n/a	n/a
6	ARID3A	chr11:46257662-46259026	K562	blood:	n/a	n/a
7	ARID3A	chr11:46275775-46275943	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:46269211-46269472	K562	blood:	n/a	n/a
9	ARID3A	chr11:46264604-46265485	K562	blood:	n/a	chr11:46265114-46265130
10	ARID3A	chr11:46272000-46272273	K562	blood:	n/a	n/a
11	ARID3A	chr11:46260638-46261132	K562	blood:	n/a	n/a
12	ARID3A	chr11:46264625-46265255	HepG2	liver:	n/a	chr11:46265114-46265130
13	ATF1	chr11:46270922-46271620	K562	blood:	n/a	n/a
14	ATF1	chr11:46269105-46269513	K562	blood:	n/a	n/a
15	ATF1	chr11:46278195-46278319	K562	blood:	n/a	n/a
16	ATF1	chr11:46264625-46265118	K562	blood:	n/a	n/a
17	ATF1	chr11:46271997-46272332	K562	blood:	n/a	n/a
18	ATF1	chr11:46258668-46259031	K562	blood:	n/a	n/a
19	ATF2	chr11:46260442-46261304	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr11:46260594-46261126	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr11:46269090-46269512	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr11:46269098-46269627	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr11:46264441-46265126	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr11:46264460-46265338	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr11:46260647-46261121	GM12878	blood:	n/a	n/a
26	ATF3	chr11:46264613-46265076	H1-hESC	embryonic stem cell:	n/a	chr11:46265061-46265070
27	ATF3	chr11:46270123-46270649	K562	blood:	n/a	n/a
28	ATF3	chr11:46259561-46259910	K562	blood:	n/a	chr11:46259863-46259878
29	ATF3	chr11:46258679-46259029	K562	blood:	n/a	n/a
30	ATF3	chr11:46262454-46262777	K562	blood:	n/a	n/a
31	ATF3	chr11:46271991-46272423	K562	blood:	n/a	n/a
32	ATF3	chr11:46264747-46265034	K562	blood:	n/a	n/a
33	ATF3	chr11:46264793-46265129	HepG2	liver:	n/a	chr11:46265061-46265070
34	ATF3	chr11:46264571-46265141	K562	blood:	n/a	chr11:46265061-46265070
35	ATF3	chr11:46258587-46259141	K562	blood:	n/a	n/a
36	BACH1	chr11:46265215-46265466	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr11:46270210-46270468	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr11:46258763-46259018	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr11:46265422-46265620	K562	blood:	n/a	n/a
40	BACH1	chr11:46260670-46261035	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr11:46261039-46261075	K562	blood:	n/a	n/a
42	BACH1	chr11:46258742-46258952	K562	blood:	n/a	n/a
43	BCL3	chr11:46264571-46265298	A549	lung:	n/a	chr11:46264624-46264633
44	BCL3	chr11:46258590-46259396	A549	lung:	n/a	chr11:46259185-46259198
45	BCL3	chr11:46260110-46261101	A549	lung:	n/a	chr11:46260698-46260711 chr11:46260781-46260790
46	BCL3	chr11:46264528-46265435	A549	lung:	n/a	chr11:46264624-46264633
47	BCLAF1	chr11:46260592-46261056	GM12878	blood:	n/a	chr11:46260698-46260711 chr11:46260781-46260790
48	BHLHE40	chr11:46273885-46274380	HepG2	liver:	n/a	n/a
49	BHLHE40	chr11:46259620-46260201	GM12878	blood:	n/a	chr11:46259949-46259965 chr11:46259628-46259644 chr11:46259950-46259966
50	BHLHE40	chr11:46259610-46260122	HepG2	liver:	n/a	chr11:46259949-46259965 chr11:46259628-46259644 chr11:46259950-46259966

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46260412-46260462	HUVEC	blood vessel:	n/a
2	chr11:46259470-46259520	RPTEC	kidney:	n/a
3	chr11:46260412-46260462	HUVEC	blood vessel:	n/a
4	chr11:46259470-46259520	RPTEC	kidney:	n/a
5	chr11:46260204-46260254	HRCEpiC	kidney:	n/a
6	chr11:46265260-46265310	ProgFib	skin:	n/a
7	chr11:46260795-46260845	AG09309	skin:	n/a
8	chr11:46260234-46260284	SKMC	muscle:	n/a
9	chr11:46260756-46260806	HRPEpiC	eye:	n/a
10	chr11:46260045-46260095	NHBE	bronchial:	n/a
11	chr11:46265076-46265126	HAEpiC	amniotic membrane:	n/a
12	chr11:46261352-46261402	K562	blood:	n/a
13	chr11:46265393-46265443	ProgFib	skin:	n/a
14	chr11:46260412-46260462	HCF	heart:	n/a
15	chr11:46260234-46260284	ECC-1	luminal epithelium:	n/a
16	chr11:46260795-46260845	LNCaP	prostate:	n/a
17	chr11:46261208-46261258	NT2-D1	testis:	n/a
18	chr11:46260234-46260284	AG04450	lung:	fetal
19	chr11:46256065-46256115	NH-A	brain:	n/a
20	chr11:46264818-46264868	HMEC	breast:	n/a
21	chr11:46265076-46265126	A549	lung:	n/a
22	chr11:46265393-46265443	RPTEC	kidney:	n/a
23	chr11:46264818-46264868	AG04450	lung:	fetal
24	chr11:46260204-46260254	GM12892	blood:	n/a
25	chr11:46260412-46260462	HepG2	liver:	n/a
26	chr11:46256065-46256115	SKMC	muscle:	n/a
27	chr11:46265260-46265310	HL-60	blood:	n/a
28	chr11:46260756-46260806	AG09309	skin:	n/a
29	chr11:46263780-46263830	ProgFib	skin:	n/a
30	chr11:46260849-46260899	HCF	heart:	n/a
31	chr11:46261208-46261258	AG04449	skin:	fetal
32	chr11:46260795-46260845	HNPCEpiC	eye:	n/a
33	chr11:46258039-46258089	HCT-116	colon:	n/a
34	chr11:46265076-46265126	GM19239	blood:	n/a
35	chr11:46258039-46258089	Hela-S3	cervix:	n/a
36	chr11:46259470-46259520	T-47D	breast:	n/a
37	chr11:46260795-46260845	PFSK-1	brain:	n/a
38	chr11:46260412-46260462	GM06990	blood:	n/a
39	chr11:46270542-46270592	MCF-7	breast:	n/a
40	chr11:46260849-46260899	HMEC	breast:	n/a
41	chr11:46264818-46264868	IMR90	lung:	fetal
42	chr11:46265134-46265184	SK-N-MC	brain:	n/a
43	chr11:46265260-46265310	MCF-7	breast:	n/a
44	chr11:46260849-46260899	GM12892	blood:	n/a
45	chr11:46265076-46265126	SAEC	small airway:	n/a
46	chr11:46260849-46260899	BE2_C	brain:	n/a
47	chr11:46270542-46270592	HEEpiC	esophagus:	n/a
48	chr11:46265260-46265310	GM12878	blood:	n/a
49	chr11:46264544-46264594	PrEC	prostate:	n/a
50	chr11:46258039-46258089	HNPCEpiC	eye:	n/a

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr11:46277054..46280118-chr11:46289490..46292654,3	MCF-7	breast:
2	chr11:46263412..46267230-chr11:46295489..46297894,3	K562	blood:
3	chr11:46239861..46241772-chr11:46260396..46261899,2	K562	blood:
4	chr11:46263045..46265873-chr11:46295785..46297445,2	MCF-7	breast:
5	chr11:46274201..46276246-chr11:46277758..46279425,2	K562	blood:
6	chr11:46260020..46262918-chr11:46267524..46269406,4	MCF-7	breast:
7	chr11:46257536..46260038-chr11:46298629..46301325,2	K562	blood:
8	chr11:46260567..46262219-chr11:46367373..46369497,2	MCF-7	breast:
9	chr11:46283499..46285311-chr11:46286883..46289251,2	K562	blood:
10	chr11:46262681..46266586-chr11:46271092..46274649,4	MCF-7	breast:
11	chr11:46259014..46262894-chr11:46335326..46342667,9	K562	blood:
12	chr11:46260392..46261346-chr11:46336358..46337814,7	K562	blood:
13	chr11:46287117..46289600-chr11:46291560..46294063,4	K562	blood:
14	chr11:46270657..46272184-chr11:46336005..46338411,2	MCF-7	breast:
15	chr11:46260034..46261360-chr11:46336245..46337600,10	MCF-7	breast:
16	chr11:46141256..46143390-chr11:46248158..46251074,3	K562	blood:
17	chr11:46263673..46265397-chr11:46397060..46399611,2	K562	blood:
18	chr11:46142521..46144729-chr11:46264687..46266930,3	MCF-7	breast:
19	chr11:46264875..46267738-chr11:46329281..46332711,3	MCF-7	breast:
20	chr11:46234295..46236778-chr11:46252794..46255230,2	K562	blood:
21	chr11:46259959..46260814-chr19:2475741..2476377,2	Hela-S3	cervix:
22	chr11:46148570..46149540-chr11:46260403..46260958,3	MCF-7	breast:
23	chr1:17231333..17231967-chr11:46264658..46265339,2	NB4	blood:
24	chr11:46263623..46265144-chr11:46301509..46304362,2	MCF-7	breast:
25	chr11:46269232..46272013-chr11:46298010..46299665,2	K562	blood:
26	chr11:46260302..46262662-chr11:46340066..46342667,3	K562	blood:
27	chr11:46267585..46269649-chr11:46335918..46338453,3	MCF-7	breast:
28	chr11:46260020..46262918-chr11:46267524..46269406,4	MCF-7	breast:
29	chr11:46236791..46240421-chr11:46247000..46248539,3	K562	blood:
30	chr11:46258602..46259157-chr6:26270982..26271725,2	Hela-S3	cervix:
31	chr11:46284336..46285851-chr11:46387966..46390716,2	MCF-7	breast:
32	chr11:46257250..46262210-chr11:46367431..46371476,7	K562	blood:
33	chr11:46258132..46262487-chr11:46262978..46267443,11	MCF-7	breast:
34	chr11:46237017..46239768-chr11:46242013..46243716,2	K562	blood:
35	chr11:46283063..46284640-chr11:46299295..46301422,2	K562	blood:
36	chr11:46269008..46269741-chr11:46330171..46330801,2	K562	blood:
37	chr11:46259959..46260523-chr2:9770425..9771131,2	Hela-S3	cervix:
38	chr11:46231907..46234628-chr11:46240321..46242392,2	K562	blood:
39	chr11:46286385..46288724-chr11:46297253..46299530,2	MCF-7	breast:
40	chr11:46268866..46269479-chr11:46559103..46559758,2	K562	blood:
41	chr11:46283499..46285311-chr11:46286883..46289251,2	K562	blood:
42	chr11:46258542..46259397-chr2:28973816..28974795,2	Hela-S3	cervix:
43	chr11:46259601..46262600-chr11:46396117..46399053,2	K562	blood:
44	chr1:97187532..97188205-chr11:46264654..46265306,2	Hela-S3	cervix:
45	chr11:46261574..46264285-chr11:46284540..46287123,3	K562	blood:
46	chr11:46278312..46279888-chr11:46315441..46317879,2	K562	blood:
47	chr11:46259169..46259902-chrX:48432781..48433319,2	Hela-S3	cervix:
48	chr11:46256874..46260563-chr11:46399060..46405748,9	K562	blood:
49	chr11:46259736..46262157-chr11:46281233..46283717,2	K562	blood:
50	chr11:46240364..46242725-chr11:46242954..46244645,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF21A-1	chr11:46242187-46242861	NONHSAT021161
2	lnc-CHRM4-1	chr11:46277871-46278092	XLOC_009437
3	lnc-CREB3L1-1	chr11:46260290-46260818	ENSG00000254639
4	lnc-CHRM4-1	chr11:46277906-46278092	ENSG00000255007.1
5	lnc-CREB3L1-1	chr11:46259933-46260056	ENSG00000254639

No data

Variant related genes	Relation type
ENSG00000255269	TF binding region
ENSG00000254639	TF binding region
ENSG00000255269	CpG island
ENSG00000254639	CpG island
ENSG00000254639	chromatin interactions
ENSG00000134308	chromatin interactions
ENSG00000100804	chromatin interactions
ENSG00000255007	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000247675	chromatin interactions
ENSG00000066427	chromatin interactions
ENSG00000265943	chromatin interactions
ENSG00000141664	chromatin interactions
ENSG00000110492	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000197429	chromatin interactions
ENSG00000099860	chromatin interactions
ENSG00000264817	chromatin interactions
ENSG00000163565	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000151881	chromatin interactions
ENSG00000102317	chromatin interactions
ENSG00000256018	chromatin interactions
ENSG00000204620	chromatin interactions
ENSG00000135365	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000264102	chromatin interactions
ENSG00000150459	chromatin interactions
ENSG00000175216	chromatin interactions
ENSG00000254653	chromatin interactions
ENSG00000244968	chromatin interactions
ENSG00000121680	chromatin interactions
ENSG00000180720	chromatin interactions
ENSG00000103194	chromatin interactions
ENSG00000213639	chromatin interactions
ENSG00000157613	chromatin interactions
ENSG00000263539	chromatin interactions
ENSG00000255269	chromatin interactions
ENSG00000113594	chromatin interactions
ENSG00000101773	chromatin interactions
ENSG00000235823	chromatin interactions
CSNK1D	miRNA target sites

Extended variants
information (count: 1539 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368579683	chr11:46242408-46242409	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs565594767	chr11:46242469-46242470	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs534649820	chr11:46242476-46242477	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs142876468	chr11:46242491-46242492	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs571379551	chr11:46242500-46242501	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs377408514	chr11:46242503-46242504	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs180859323	chr11:46242526-46242527	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs370355889	chr11:46242585-46242586	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs574205205	chr11:46242665-46242666	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs151050911	chr11:46242669-46242670	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs139930845	chr11:46242698-46242699	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs373019054	chr11:46242728-46242729	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs186084675	chr11:46242733-46242734	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs545426329	chr11:46242789-46242790	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs565456238	chr11:46242807-46242808	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs192108807	chr11:46242949-46242950	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs35986466	chr11:46242960-46242961	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs199551760	chr11:46243094-46243095	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs183189908	chr11:46243137-46243138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs143339477	chr11:46243140-46243141	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs562996914	chr11:46243315-46243316	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201734209	chr11:46243373-46243374	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs528964844	chr11:46243383-46243384	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs146719454	chr11:46243386-46243387	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs34104695	chr11:46243436-46243437	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs185979858	chr11:46243520-46243521	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs77722161	chr11:46243530-46243531	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs528363972	chr11:46243539-46243540	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190588926	chr11:46243540-46243541	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs140454026	chr11:46243614-46243615	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs536818182	chr11:46243648-46243649	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs570704953	chr11:46243769-46243770	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs557196072	chr11:46243772-46243773	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567725843	chr11:46243901-46243902	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536786883	chr11:46243922-46243923	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs539693817	chr11:46244012-46244013	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs553401896	chr11:46244125-46244126	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs573186663	chr11:46244153-46244154	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs375960976	chr11:46244173-46244174	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs545398979	chr11:46244178-46244179	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs558955397	chr11:46244244-46244245	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575894590	chr11:46244271-46244272	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs527848239	chr11:46244314-46244315	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs528698687	chr11:46244321-46244322	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs71451639	chr11:46244325-46244326	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs144897594	chr11:46244340-46244341	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs111791155	chr11:46244369-46244370	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs556342372	chr11:46244375-46244376	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs573398528	chr11:46244419-46244420	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs75705776	chr11:46244460-46244461	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1581 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46241400-46244200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:46241800-46242600	Enhancers	K562	blood
3	chr11:46242600-46243000	Weak transcription	K562	blood
4	chr11:46243000-46244000	Enhancers	K562	blood
5	chr11:46243600-46244600	Enhancers	Brain Germinal Matrix	brain
6	chr11:46244000-46244200	Flanking Active TSS	K562	blood
7	chr11:46244200-46244400	Enhancers	K562	blood
8	chr11:46244200-46244600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:46244200-46244600	Enhancers	Brain Cingulate Gyrus	brain
10	chr11:46244200-46244600	Enhancers	Fetal Lung	lung
11	chr11:46244200-46244800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr11:46244200-46244800	Enhancers	Hela-S3	cervix
13	chr11:46244200-46245000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:46244400-46244600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr11:46244400-46244600	Flanking Active TSS	K562	blood
16	chr11:46244400-46245000	Enhancers	HepG2	liver
17	chr11:46244400-46245400	Enhancers	Duodenum Mucosa	Duodenum
18	chr11:46244600-46245000	Enhancers	Fetal Intestine Small	intestine
19	chr11:46244600-46245000	Enhancers	Spleen	Spleen
20	chr11:46244600-46245400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr11:46244600-46246000	Enhancers	K562	blood
22	chr11:46245800-46246000	Enhancers	Duodenum Mucosa	Duodenum
23	chr11:46246000-46249600	Weak transcription	K562	blood
24	chr11:46249600-46250600	Enhancers	K562	blood
25	chr11:46250600-46253400	Weak transcription	K562	blood
26	chr11:46250800-46251000	Enhancers	Placenta	Placenta
27	chr11:46250800-46251000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr11:46251000-46258400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr11:46251200-46251400	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr11:46253400-46253600	Enhancers	K562	blood
31	chr11:46253600-46254200	Weak transcription	K562	blood
32	chr11:46254200-46254400	Enhancers	K562	blood
33	chr11:46254800-46255200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
34	chr11:46255400-46256400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr11:46255600-46255800	Enhancers	H9 Cell Line	embryonic stem cell
36	chr11:46255600-46256000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr11:46255600-46256000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr11:46255600-46256200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr11:46255600-46256400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr11:46255600-46256400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:46255600-46256400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:46255600-46256400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
43	chr11:46255600-46256400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr11:46255600-46256400	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr11:46255800-46256000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr11:46255800-46256000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
47	chr11:46255800-46256400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr11:46255800-46258600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr11:46256000-46256200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr11:46256000-46256200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell

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