Variant report

Variant	esv1829985
Chromosome Location	chr11:85740319-85789350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1683)
CpG islands
(count:917)
Chromatin interactive
region (count:116)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1683 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:85752416-85752519	K562	blood:	n/a	n/a
2	ARID3A	chr11:85746984-85746991	K562	blood:	n/a	n/a
3	ARID3A	chr11:85777674-85778973	HepG2	liver:	n/a	chr11:85778090-85778106 chr11:85778089-85778105
4	ARID3A	chr11:85748985-85749017	K562	blood:	n/a	n/a
5	ARID3A	chr11:85777550-85778983	K562	blood:	n/a	chr11:85778090-85778106 chr11:85778089-85778105
6	ARID3A	chr11:85780725-85781123	K562	blood:	n/a	n/a
7	ARID3A	chr11:85775931-85776327	K562	blood:	n/a	n/a
8	ARID3A	chr11:85752905-85753433	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:85780014-85780600	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:85779200-85779533	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:85755776-85755794	K562	blood:	n/a	n/a
12	ARID3A	chr11:85745847-85746142	K562	blood:	n/a	chr11:85746093-85746109
13	ARID3A	chr11:85784608-85784808	K562	blood:	n/a	n/a
14	ARID3A	chr11:85752889-85753338	K562	blood:	n/a	n/a
15	ARID3A	chr11:85757105-85757526	K562	blood:	n/a	n/a
16	ARID3A	chr11:85774575-85775592	K562	blood:	n/a	n/a
17	ARID3A	chr11:85782479-85782542	K562	blood:	n/a	n/a
18	ATF1	chr11:85773901-85773935	K562	blood:	n/a	n/a
19	ATF1	chr11:85780076-85781186	K562	blood:	n/a	n/a
20	ATF1	chr11:85752964-85753255	K562	blood:	n/a	n/a
21	ATF1	chr11:85778379-85778980	K562	blood:	n/a	n/a
22	ATF2	chr11:85780002-85780414	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr11:85780722-85781161	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr11:85780180-85781254	GM12878	blood:	n/a	n/a
25	ATF2	chr11:85779976-85781265	GM12878	blood:	n/a	n/a
26	ATF2	chr11:85752892-85753316	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr11:85779936-85780575	GM12878	blood:	n/a	chr11:85780156-85780176 chr11:85780167-85780187 chr11:85780351-85780360 chr11:85780272-85780292 chr11:85780167-85780176
28	ATF3	chr11:85779987-85780504	K562	blood:	n/a	chr11:85780156-85780176 chr11:85780167-85780187 chr11:85780351-85780360 chr11:85780272-85780292 chr11:85780167-85780176
29	ATF3	chr11:85779996-85780424	H1-hESC	embryonic stem cell:	n/a	chr11:85780156-85780176 chr11:85780167-85780187 chr11:85780351-85780360 chr11:85780272-85780292 chr11:85780167-85780176
30	ATF3	chr11:85780255-85780408	GM12878	blood:	n/a	chr11:85780351-85780360 chr11:85780272-85780292
31	ATF3	chr11:85779875-85780416	H1-hESC	embryonic stem cell:	n/a	chr11:85780156-85780176 chr11:85780167-85780187 chr11:85780351-85780360 chr11:85780272-85780292 chr11:85780167-85780176
32	ATF3	chr11:85779993-85780425	HepG2	liver:	n/a	chr11:85780156-85780176 chr11:85780167-85780187 chr11:85780351-85780360 chr11:85780272-85780292 chr11:85780167-85780176
33	ATF3	chr11:85775239-85775606	K562	blood:	n/a	n/a
34	ATF3	chr11:85780466-85781148	K562	blood:	n/a	n/a
35	BACH1	chr11:85778267-85778322	K562	blood:	n/a	n/a
36	BACH1	chr11:85747287-85747355	K562	blood:	n/a	n/a
37	BACH1	chr11:85780167-85780457	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr11:85778753-85778868	K562	blood:	n/a	n/a
39	BACH1	chr11:85782656-85782662	K562	blood:	n/a	n/a
40	BATF	chr11:85759660-85760022	GM12878	blood:	n/a	n/a
41	BATF	chr11:85758299-85758659	GM12878	blood:	n/a	chr11:85758485-85758496
42	BATF	chr11:85780430-85780705	GM12878	blood:	n/a	n/a
43	BATF	chr11:85758286-85758651	GM12878	blood:	n/a	chr11:85758485-85758496
44	BATF	chr11:85780831-85781159	GM12878	blood:	n/a	chr11:85780956-85780969
45	BCL3	chr11:85779958-85780682	GM12878	blood:	n/a	n/a
46	BCLAF1	chr11:85752911-85753373	GM12878	blood:	n/a	n/a
47	BCLAF1	chr11:85779226-85781234	GM12878	blood:	n/a	chr11:85781030-85781039 chr11:85779502-85779511
48	BCLAF1	chr11:85778076-85778673	GM12878	blood:	n/a	n/a
49	BHLHE40	chr11:85783040-85783126	K562	blood:	n/a	n/a
50	BHLHE40	chr11:85748794-85748974	K562	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:85783475-85783525	AG04449	skin:	fetal
2	chr11:85783475-85783525	GM12878	blood:	n/a
3	chr11:85783475-85783525	AG04449	skin:	fetal
4	chr11:85783475-85783525	GM12878	blood:	n/a
5	chr11:85783475-85783525	BE2_C	brain:	n/a
6	chr11:85778241-85778291	SK-N-SH_RA	brain:	n/a
7	chr11:85772935-85772985	AG04449	skin:	fetal
8	chr11:85778585-85778635	PANC-1	pancreas:	n/a
9	chr11:85780029-85780079	SKMC	muscle:	n/a
10	chr11:85780144-85780194	MCF-7	breast:	n/a
11	chr11:85778241-85778291	H1-hESC	embryonic stem cell:	embryo
12	chr11:85780378-85780428	NT2-D1	testis:	n/a
13	chr11:85780129-85780179	SKMC	muscle:	n/a
14	chr11:85755155-85755205	AG04449	skin:	fetal
15	chr11:85753082-85753132	HAEpiC	amniotic membrane:	n/a
16	chr11:85780144-85780194	AG09319	gingival:	n/a
17	chr11:85778585-85778635	HEEpiC	esophagus:	n/a
18	chr11:85780129-85780179	AG04450	lung:	fetal
19	chr11:85780144-85780194	SKMC	muscle:	n/a
20	chr11:85780029-85780079	MCF10A-Er-Src	breast:	n/a
21	chr11:85780029-85780079	PrEC	prostate:	n/a
22	chr11:85755155-85755205	Jurkat	blood:	n/a
23	chr11:85778585-85778635	ProgFib	skin:	n/a
24	chr11:85780378-85780428	RPTEC	kidney:	n/a
25	chr11:85783475-85783525	AG04450	lung:	fetal
26	chr11:85783475-85783525	HAEpiC	amniotic membrane:	n/a
27	chr11:85780971-85781021	SKMC	muscle:	n/a
28	chr11:85753082-85753132	K562	blood:	n/a
29	chr11:85780129-85780179	AG09309	skin:	n/a
30	chr11:85780029-85780079	ovcar-3	ovarian:	n/a
31	chr11:85783475-85783525	MCF-7	breast:	n/a
32	chr11:85780378-85780428	A549	lung:	n/a
33	chr11:85783475-85783525	SK-N-MC	brain:	n/a
34	chr11:85780144-85780194	AG10803	skin:	n/a
35	chr11:85780144-85780194	RPTEC	kidney:	n/a
36	chr11:85780971-85781021	PFSK-1	brain:	n/a
37	chr11:85744995-85745045	GM06990	blood:	n/a
38	chr11:85780971-85781021	GM12878	blood:	n/a
39	chr11:85780971-85781021	K562	blood:	n/a
40	chr11:85780971-85781021	PrEC	prostate:	n/a
41	chr11:85778585-85778635	HL-60	blood:	n/a
42	chr11:85783475-85783525	AG09319	gingival:	n/a
43	chr11:85783475-85783525	A549	lung:	n/a
44	chr11:85755155-85755205	GM12892	blood:	n/a
45	chr11:85779252-85779302	K562	blood:	n/a
46	chr11:85780378-85780428	LNCaP	prostate:	n/a
47	chr11:85780144-85780194	HRPEpiC	eye:	n/a
48	chr11:85779252-85779302	HCM	heart:	n/a
49	chr11:85778585-85778635	NH-A	brain:	n/a
50	chr11:85780971-85781021	HEEpiC	esophagus:	n/a

(count:116 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:85781558..85783206-chr11:85914108..85916095,2	K562	blood:
2	chr11:85741019..85743980-chr11:85750116..85753197,4	K562	blood:
3	chr11:85702541..85705321-chr11:85738673..85740319,2	K562	blood:
4	chr11:85752937..85753595-chr11:85904443..85905270,7	MCF-7	breast:
5	chr11:85775017..85777690-chr11:85953768..85955485,2	K562	blood:
6	chr11:85752045..85752748-chr11:85904571..85905268,2	MCF-7	breast:
7	chr11:85769113..85770069-chr12:72057058..72057892,2	Hela-S3	cervix:
8	chr11:85763624..85765571-chr11:85766544..85768269,2	MCF-7	breast:
9	chr11:85739064..85744454-chr11:85744719..85749528,8	K562	blood:
10	chr11:85745012..85747754-chr11:85749922..85752779,3	MCF-7	breast:
11	chr11:85780388..85781944-chr11:85788305..85790883,2	MCF-7	breast:
12	chr11:85756990..85760040-chr11:85954686..85957890,3	K562	blood:
13	chr11:85779286..85779918-chr3:47422174..47422744,2	Hela-S3	cervix:
14	chr11:85753896..85756405-chr11:85894218..85896804,2	K562	blood:
15	chr11:85779754..85780343-chr13:111367026..111368006,2	Hela-S3	cervix:
16	chr11:85758317..85760052-chr11:85763851..85765392,2	MCF-7	breast:
17	chr11:85780341..85780869-chr8:97247422..97248307,2	NB4	blood:
18	chr11:85775018..85777414-chr11:85781077..85783520,2	K562	blood:
19	chr11:85754103..85756697-chr11:85903724..85906078,2	K562	blood:
20	chr11:85740366..85741884-chr11:85743938..85745486,2	MCF-7	breast:
21	chr11:85753212..85755619-chr11:85956266..85958144,2	K562	blood:
22	chr11:85375979..85377499-chr11:85779750..85781435,2	K562	blood:
23	chr11:85760823..85766402-chr11:85776742..85780604,5	K562	blood:
24	chr11:85754219..85755757-chr11:85998190..86001098,2	K562	blood:
25	chr1:149783817..149784624-chr11:85780019..85780945,2	HCT-116	colon:
26	chr11:85779839..85780644-chr16:50099773..50100446,2	NB4	blood:
27	chr11:85752345..85755214-chr11:85762057..85763811,2	K562	blood:
28	chr11:85752432..85754152-chr11:85778326..85779927,2	K562	blood:
29	chr11:85764603..85768167-chr11:85770443..85773239,4	K562	blood:
30	chr11:85740366..85741884-chr11:85743938..85745486,2	MCF-7	breast:
31	chr11:85752580..85754495-chr11:85817812..85820593,2	K562	blood:
32	chr11:85759040..85760560-chr11:85914409..85916146,2	K562	blood:
33	chr11:85768733..85771194-chr11:85773077..85775713,3	MCF-7	breast:
34	chr11:85746383..85749282-chr11:85752081..85754619,3	K562	blood:
35	chr11:85752681..85753613-chr11:85986298..85987019,2	K562	blood:
36	chr11:85763823..85764323-chr2:47404075..47404578,2	Hela-S3	cervix:
37	chr11:85758317..85760052-chr11:85763851..85765392,2	MCF-7	breast:
38	chr11:85520681..85523600-chr11:85778386..85780657,2	MCF-7	breast:
39	chr11:85774012..85776185-chr11:85778129..85779860,2	MCF-7	breast:
40	chr11:85759414..85762040-chr11:85764190..85765879,2	K562	blood:
41	chr11:85752653..85753611-chr11:85929070..85929776,5	K562	blood:
42	chr11:85750753..85754921-chr11:85777860..85781815,4	MCF-7	breast:
43	chr11:85744471..85746960-chr11:85953530..85956105,2	K562	blood:
44	chr11:85733299..85737465-chr11:85737887..85740923,4	MCF-7	breast:
45	chr11:85779917..85781059-chr11:85904304..85905143,3	K562	blood:
46	chr11:85774766..85777240-chr11:85903999..85905671,2	K562	blood:
47	chr11:85776467..85780584-chr11:85902948..85906650,5	MCF-7	breast:
48	chr11:85775786..85777864-chr11:85954494..85956140,2	MCF-7	breast:
49	chr11:85768733..85771194-chr11:85773077..85775713,3	MCF-7	breast:
50	chr11:85763399..85766390-chr11:85766683..85769520,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC83-2	chr11:85779372-85780094	NONHSAT023456
2	lnc-CCDC83-2	chr11:85783360-85783401	NONHSAT023456

No data

Variant related genes	Relation type
PICALM	TF binding region
PICALM	CpG island
ENSG00000073921	chromatin interactions
ENSG00000155393	chromatin interactions
ENSG00000121350	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000260236	chromatin interactions
ENSG00000254502	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000259843	chromatin interactions
ENSG00000254224	chromatin interactions
ENSG00000203814	chromatin interactions
ENSG00000076201	chromatin interactions
ENSG00000158769	chromatin interactions
ENSG00000254699	chromatin interactions
ENSG00000137504	chromatin interactions
ENSG00000074266	chromatin interactions
ENSG00000133858	chromatin interactions
ENSG00000156467	chromatin interactions
ENSG00000137501	chromatin interactions
ENSG00000146731	chromatin interactions
ENSG00000200877	chromatin interactions

Extended variants
information (count: 2023 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2023 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs609903	chr11:85740409-85740410	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11234518	chr11:85740428-85740429	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs561047183	chr11:85740439-85740440	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs538570579	chr11:85740457-85740458	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs556582177	chr11:85740464-85740465	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs112848653	chr11:85740479-85740480	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs182653745	chr11:85740480-85740481	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531564436	chr11:85740524-85740525	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538873606	chr11:85740583-85740584	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554325745	chr11:85740597-85740598	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs17817859	chr11:85740642-85740643	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35892073	chr11:85740645-85740646	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114523005	chr11:85740680-85740681	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs571478451	chr11:85740687-85740688	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs538560654	chr11:85740718-85740719	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs186928547	chr11:85740721-85740722	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs576034442	chr11:85740730-85740731	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs543755987	chr11:85740736-85740737	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs565057571	chr11:85740761-85740762	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532404164	chr11:85740773-85740774	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs540905022	chr11:85740789-85740790	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs189804829	chr11:85740798-85740799	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs529863420	chr11:85740856-85740857	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs182381580	chr11:85740857-85740858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150765281	chr11:85740879-85740880	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs189066084	chr11:85740891-85740892	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs193149459	chr11:85740897-85740898	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs76329148	chr11:85740906-85740907	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs367983829	chr11:85740908-85740909	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571880792	chr11:85741035-85741036	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs185638768	chr11:85741058-85741059	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs149533304	chr11:85741102-85741103	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs682928	chr11:85741130-85741131	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs565583366	chr11:85741159-85741160	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs116375405	chr11:85741165-85741166	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs576456558	chr11:85741223-85741224	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs537068639	chr11:85741239-85741240	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs558898317	chr11:85741321-85741322	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs144150222	chr11:85741366-85741367	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs188503985	chr11:85741409-85741410	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs11234519	chr11:85741422-85741423	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs574693746	chr11:85741450-85741451	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184251986	chr11:85741451-85741452	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs139787823	chr11:85741489-85741490	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs74594598	chr11:85741495-85741496	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs188549773	chr11:85741500-85741501	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs564103801	chr11:85741508-85741509	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs180916786	chr11:85741531-85741532	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs547691827	chr11:85741538-85741539	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371936718	chr11:85741543-85741544	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
Obesity	20622171	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2473 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85659400-85745800	Weak transcription	Stomach Mucosa	stomach
2	chr11:85665200-85742600	Strong transcription	Primary T helper cells fromperipheralblood	blood
3	chr11:85665200-85743000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr11:85675000-85742600	Strong transcription	Primary B cells from peripheral blood	blood
5	chr11:85697800-85742600	Strong transcription	HUVEC	blood vessel
6	chr11:85700600-85742400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr11:85701000-85745000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr11:85703200-85742800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:85712800-85740800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:85712800-85741600	Weak transcription	Aorta	Aorta
11	chr11:85712800-85743400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr11:85716600-85741400	Weak transcription	Fetal Heart	heart
13	chr11:85716800-85746200	Weak transcription	Pancreas	Pancrea
14	chr11:85719800-85743400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:85720400-85742600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr11:85720800-85742600	Strong transcription	HSMM	muscle
17	chr11:85721800-85745800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr11:85725600-85742800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr11:85727200-85741800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:85727200-85742000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr11:85727800-85741800	Strong transcription	Liver	Liver
22	chr11:85727800-85745800	Weak transcription	Right Ventricle	heart
23	chr11:85728600-85742000	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr11:85729800-85742600	Strong transcription	Osteobl	bone
25	chr11:85730000-85742000	Strong transcription	NHDF-Ad	bronchial
26	chr11:85730000-85742400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr11:85730000-85742400	Strong transcription	Fetal Thymus	thymus
28	chr11:85730000-85742600	Strong transcription	Placenta	Placenta
29	chr11:85730200-85742600	Strong transcription	Fetal Lung	lung
30	chr11:85730600-85743200	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr11:85730800-85742200	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr11:85730800-85742600	Strong transcription	Dnd41	blood
33	chr11:85731600-85754200	Weak transcription	Brain Germinal Matrix	brain
34	chr11:85732200-85744600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr11:85732600-85742400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:85732600-85743000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr11:85732800-85742600	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr11:85732800-85744000	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr11:85733200-85742800	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr11:85733200-85754000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr11:85733400-85742400	Strong transcription	Primary hematopoietic stem cells	blood
42	chr11:85733400-85742600	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr11:85733800-85743000	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr11:85734000-85742600	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr11:85734200-85740600	Strong transcription	A549	lung
46	chr11:85734200-85742200	Strong transcription	Primary T cells from cord blood	blood
47	chr11:85734200-85742400	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr11:85734200-85742400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:85734200-85742400	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr11:85734200-85742600	Strong transcription	Adipose Nuclei	Adipose

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