Variant report

Variant	nsv825960
Chromosome Location	chr11:67238644-67250833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:664)
CpG islands
(count:1039)
Chromatin interactive
region (count:59)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:67250656-67250988	K562	blood:	n/a	n/a
2	ARID3A	chr11:67249949-67250047	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:67250520-67250884	HepG2	liver:	n/a	n/a
4	ATF1	chr11:67250338-67250977	K562	blood:	n/a	n/a
5	ATF2	chr11:67250279-67250828	GM12878	blood:	n/a	n/a
6	ATF2	chr11:67250386-67250993	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:67249743-67250222	GM12878	blood:	n/a	n/a
8	ATF3	chr11:67250316-67251116	A549	lung:	n/a	chr11:67250910-67250919
9	ATF3	chr11:67250430-67251046	A549	lung:	n/a	chr11:67250910-67250919
10	BACH1	chr11:67250770-67250852	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr11:67249869-67250197	GM12878	blood:	n/a	chr11:67250035-67250045
12	BATF	chr11:67249729-67250181	GM12878	blood:	n/a	chr11:67250035-67250045
13	BCL3	chr11:67250423-67251061	A549	lung:	n/a	chr11:67250423-67250432 chr11:67250910-67250923
14	BCLAF1	chr11:67249750-67250369	GM12878	blood:	n/a	chr11:67250033-67250042 chr11:67250034-67250043 chr11:67250242-67250251
15	BCLAF1	chr11:67250482-67251077	GM12878	blood:	n/a	chr11:67250910-67250923
16	BHLHE40	chr11:67250256-67251017	K562	blood:	n/a	n/a
17	BHLHE40	chr11:67250145-67250999	GM12878	blood:	n/a	n/a
18	BRCA1	chr11:67250107-67250938	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr11:67250434-67250847	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr11:67250491-67251224	GM12878	blood:	n/a	n/a
21	BRCA1	chr11:67250604-67250733	HepG2	liver:	n/a	n/a
22	CBX3	chr11:67243990-67244610	K562	blood:	n/a	n/a
23	CBX3	chr11:67250376-67251041	K562	blood:	n/a	n/a
24	CBX3	chr11:67250287-67251149	K562	blood:	n/a	n/a
25	CCNT2	chr11:67250270-67250865	K562	blood:	n/a	n/a
26	CEBPB	chr11:67250560-67251178	GM12878	blood:	n/a	n/a
27	CEBPB	chr11:67250515-67250844	HepG2	liver:	n/a	n/a
28	CEBPB	chr11:67250500-67250780	K562	blood:	n/a	n/a
29	CEBPB	chr11:67248549-67248600	A549	lung:	n/a	chr11:67248553-67248564
30	CEBPB	chr11:67249827-67250506	GM12878	blood:	n/a	n/a
31	CEBPB	chr11:67241688-67241917	HepG2	liver:	n/a	n/a
32	CEBPB	chr11:67248515-67248642	HepG2	liver:	n/a	chr11:67248553-67248564
33	CEBPB	chr11:67241671-67241867	MCF-7	breast:	n/a	n/a
34	CEBPB	chr11:67241685-67241820	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:67250542-67250888	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr11:67248470-67248664	K562	blood:	n/a	chr11:67248553-67248564
37	CEBPB	chr11:67250383-67250869	Hela-S3	cervix:	n/a	n/a
38	CEBPD	chr11:67250258-67250928	HepG2	liver:	n/a	n/a
39	CHD1	chr11:67249875-67250987	GM12878	blood:	n/a	chr11:67250780-67250790
40	CHD2	chr11:67250365-67251116	H1-hESC	embryonic stem cell:	n/a	chr11:67250780-67250790
41	CHD2	chr11:67250480-67250896	HepG2	liver:	n/a	chr11:67250780-67250790
42	CHD2	chr11:67250419-67251036	K562	blood:	n/a	chr11:67250780-67250790
43	CHD2	chr11:67250310-67251053	Hela-S3	cervix:	n/a	chr11:67250780-67250790
44	CHD2	chr11:67250260-67251099	GM12878	blood:	n/a	chr11:67250780-67250790
45	CREB1	chr11:67250237-67250630	A549	lung:	n/a	n/a
46	CREB1	chr11:67250205-67251140	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr11:67250219-67250663	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr11:67250258-67251043	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr11:67250105-67251217	HepG2	liver:	n/a	n/a
50	CREB1	chr11:67250152-67250944	A549	lung:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67250585-67250635	RPTEC	kidney:	n/a
2	chr11:67250585-67250635	HCF	heart:	n/a
3	chr11:67250585-67250635	RPTEC	kidney:	n/a
4	chr11:67250585-67250635	HCF	heart:	n/a
5	chr11:67242162-67242212	PrEC	prostate:	n/a
6	chr11:67250427-67250477	A549	lung:	n/a
7	chr11:67250164-67250214	Jurkat	blood:	n/a
8	chr11:67250445-67250495	AG10803	skin:	n/a
9	chr11:67250445-67250495	HCPEpiC	choroid plexus:	n/a
10	chr11:67250360-67250410	HMEC	breast:	n/a
11	chr11:67250360-67250410	SK-N-SH_RA	brain:	n/a
12	chr11:67250351-67250401	T-47D	breast:	n/a
13	chr11:67250052-67250102	GM19239	blood:	n/a
14	chr11:67250351-67250401	GM19239	blood:	n/a
15	chr11:67250351-67250401	HCM	heart:	n/a
16	chr11:67242162-67242212	AoSMC	blood vessel:	n/a
17	chr11:67250445-67250495	SAEC	small airway:	n/a
18	chr11:67250360-67250410	MCF10A-Er-Src	breast:	n/a
19	chr11:67250445-67250495	HCT-116	colon:	n/a
20	chr11:67250351-67250401	HCPEpiC	choroid plexus:	n/a
21	chr11:67250445-67250495	SKMC	muscle:	n/a
22	chr11:67250052-67250102	HUVEC	blood vessel:	n/a
23	chr11:67250052-67250102	RPTEC	kidney:	n/a
24	chr11:67250427-67250477	AoSMC	blood vessel:	n/a
25	chr11:67250052-67250102	T-47D	breast:	n/a
26	chr11:67250427-67250477	MCF-7	breast:	n/a
27	chr11:67250427-67250477	Jurkat	blood:	n/a
28	chr11:67250585-67250635	HUVEC	blood vessel:	n/a
29	chr11:67244585-67244635	PrEC	prostate:	n/a
30	chr11:67250585-67250635	MCF-7	breast:	n/a
31	chr11:67250164-67250214	NH-A	brain:	n/a
32	chr11:67250585-67250635	K562	blood:	n/a
33	chr11:67244585-67244635	ProgFib	skin:	n/a
34	chr11:67243955-67244005	IMR90	lung:	fetal
35	chr11:67244585-67244635	SKMC	muscle:	n/a
36	chr11:67250427-67250477	IMR90	lung:	fetal
37	chr11:67250618-67250668	HCPEpiC	choroid plexus:	n/a
38	chr11:67250052-67250102	MCF-7	breast:	n/a
39	chr11:67250309-67250359	CMK	blood:	n/a
40	chr11:67250809-67250859	Caco-2	colon:	n/a
41	chr11:67246792-67246842	AG09309	skin:	n/a
42	chr11:67250445-67250495	Hela-S3	cervix:	n/a
43	chr11:67243955-67244005	NHBE	bronchial:	n/a
44	chr11:67250618-67250668	HRPEpiC	eye:	n/a
45	chr11:67250046-67250096	NB4	blood:	n/a
46	chr11:67250445-67250495	HRE	kidney:	n/a
47	chr11:67250585-67250635	ovcar-3	ovarian:	n/a
48	chr11:67246792-67246842	NHBE	bronchial:	n/a
49	chr11:67239107-67239157	H1-hESC	embryonic stem cell:	embryo
50	chr11:67250351-67250401	NB4	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:67209268..67211659-chr11:67240314..67241828,2	K562	blood:
2	chr11:67169616..67172754-chr11:67249059..67251001,3	MCF-7	breast:
3	chr11:67250506..67252570-chr11:67374037..67375559,2	K562	blood:
4	chr11:67168054..67171427-chr11:67236833..67240975,3	K562	blood:
5	chr11:67229201..67234493-chr11:67238873..67243354,7	MCF-7	breast:
6	chr11:67250656..67253599-chr11:67256113..67260551,5	K562	blood:
7	chr11:67121864..67124508-chr11:67250272..67251792,2	K562	blood:
8	chr11:67137032..67142528-chr11:67234580..67238729,6	MCF-7	breast:
9	chr11:67171679..67173695-chr11:67249098..67251684,2	MCF-7	breast:
10	chr11:66108355..66110449-chr11:67247650..67250457,2	K562	blood:
11	chr11:67218425..67221198-chr11:67239280..67241833,2	K562	blood:
12	chr11:67235776..67238484-chr11:67248509..67251813,3	K562	blood:
13	chr11:67119767..67122418-chr11:67248932..67250571,2	MCF-7	breast:
14	chr11:67204772..67206774-chr11:67250564..67253520,2	K562	blood:
15	chr11:67236383..67238554-chr11:67244511..67246808,2	K562	blood:
16	chr11:67185175..67187264-chr11:67247117..67248962,2	K562	blood:
17	chr11:67187290..67189722-chr11:67250373..67251986,2	K562	blood:
18	chr11:67174480..67177168-chr11:67249396..67252040,3	MCF-7	breast:
19	chr11:67241990..67244752-chr11:67249224..67250775,2	MCF-7	breast:
20	chr11:67186236..67188568-chr11:67242107..67244785,2	MCF-7	breast:
21	chr11:67236926..67239757-chr11:67244854..67246808,3	K562	blood:
22	chr11:67242078..67244147-chr11:67266821..67268690,2	K562	blood:
23	chr11:67167204..67171216-chr11:67247088..67251861,5	K562	blood:
24	chr11:67247191..67252288-chr11:67270350..67277699,12	MCF-7	breast:
25	chr11:67138872..67142169-chr11:67249496..67254071,4	MCF-7	breast:
26	chr11:67229962..67234772-chr11:67234827..67242516,28	K562	blood:
27	chr11:67166860..67168425-chr11:67240476..67242002,2	MCF-7	breast:
28	chr11:67249840..67250624-chr21:40177263..40178201,2	Hela-S3	cervix:
29	chr11:67250119..67250751-chr5:43483753..43484361,2	Hela-S3	cervix:
30	chr11:67249454..67253550-chr11:67271231..67274487,6	MCF-7	breast:
31	chr11:67205296..67207654-chr11:67248873..67250891,2	MCF-7	breast:
32	chr11:67236926..67239757-chr11:67244854..67246808,3	K562	blood:
33	chr11:67231198..67233116-chr11:67249356..67252066,3	K562	blood:
34	chr11:67078757..67080884-chr11:67248865..67250419,2	MCF-7	breast:
35	chr11:67230622..67232854-chr11:67248914..67251189,3	MCF-7	breast:
36	chr11:67245999..67248702-chr11:67249047..67251747,2	K562	blood:
37	chr11:67222200..67224356-chr11:67249381..67251101,2	MCF-7	breast:
38	chr11:67249912..67253635-chr11:67270546..67273534,5	K562	blood:
39	chr11:67168541..67170644-chr11:67250058..67251865,2	MCF-7	breast:
40	chr11:67230145..67233819-chr11:67248914..67252066,4	K562	blood:
41	chr11:67250658..67253558-chr11:67351233..67353250,2	K562	blood:
42	chr11:67249113..67250802-chr11:67267518..67269287,2	MCF-7	breast:
43	chr11:67239168..67241021-chr11:67256914..67258596,2	MCF-7	breast:
44	chr11:67250117..67252279-chr11:67255664..67259072,3	MCF-7	breast:
45	chr11:67236562..67239497-chr8:145633636..145636421,2	MCF-7	breast:
46	chr11:67250774..67252740-chr11:67267582..67269484,2	MCF-7	breast:
47	chr11:67177350..67179552-chr11:67244883..67247528,2	K562	blood:
48	chr11:67167204..67172690-chr11:67247088..67251861,6	K562	blood:
49	chr11:67201373..67203481-chr11:67248801..67250929,2	MCF-7	breast:
50	chr11:67248902..67250580-chr11:67397278..67399388,2	K562	blood:

No data

Variant related genes	Relation type
AIP	TF binding region
TMEM134	TF binding region
AIP	CpG island
TMEM134	CpG island
ENSG00000172508	chromatin interactions
ENSG00000172725	chromatin interactions
ENSG00000172663	chromatin interactions
ENSG00000084207	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000110697	chromatin interactions
ENSG00000256514	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000172613	chromatin interactions
ENSG00000175463	chromatin interactions
ENSG00000167792	chromatin interactions
ENSG00000272115	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000174744	chromatin interactions
ENSG00000110711	chromatin interactions
ENSG00000071894	chromatin interactions
ENSG00000175514	chromatin interactions
ENSG00000157557	chromatin interactions
ENSG00000175544	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000175482	chromatin interactions
ENSG00000255949	chromatin interactions
ENSG00000184224	chromatin interactions
ENSG00000172531	chromatin interactions
ENSG00000151881	chromatin interactions
ENSG00000172830	chromatin interactions
ENSG00000270169	chromatin interactions
ENSG00000213402	chromatin interactions

Extended variants
information (count: 471 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112448880	chr11:67238669-67238670	Weak transcription Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs113312537	chr11:67238742-67238743	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs530530413	chr11:67238757-67238758	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs12793422	chr11:67238766-67238767	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs551920883	chr11:67238787-67238788	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs562537118	chr11:67238793-67238794	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs370467348	chr11:67238794-67238795	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs548310526	chr11:67238823-67238824	Weak transcription Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs566230648	chr11:67238828-67238829	Weak transcription Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs575761707	chr11:67238835-67238836	Weak transcription Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs543241326	chr11:67238863-67238864	Weak transcription Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs527443359	chr11:67238872-67238873	Weak transcription Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs182374786	chr11:67238885-67238886	Weak transcription Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs570384385	chr11:67238893-67238894	Weak transcription Bivalent Enhancer Active TSS Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs186720698	chr11:67238973-67238974	Weak transcription Bivalent Enhancer Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs556270233	chr11:67238974-67238975	Weak transcription Bivalent Enhancer Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs568483033	chr11:67239000-67239001	Weak transcription Bivalent Enhancer Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs561878801	chr11:67239003-67239004	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs535575017	chr11:67239007-67239008	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs143836672	chr11:67239107-67239108	Weak transcription Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs1632616	chr11:67239122-67239123	Weak transcription Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs546386914	chr11:67239152-67239153	Weak transcription Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs190886836	chr11:67239182-67239183	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs546860680	chr11:67239234-67239235	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs371812527	chr11:67239239-67239240	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs576641582	chr11:67239266-67239267	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs111901284	chr11:67239328-67239329	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs562338776	chr11:67239336-67239337	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs574325220	chr11:67239340-67239341	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs373747629	chr11:67239387-67239388	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs182508700	chr11:67239440-67239441	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs370705728	chr11:67239534-67239535	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs112039476	chr11:67239573-67239574	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs140703597	chr11:67239577-67239578	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs527405754	chr11:67239584-67239585	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs375313273	chr11:67239629-67239630	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs189159309	chr11:67239651-67239652	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs535837534	chr11:67239680-67239681	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs531499117	chr11:67239780-67239781	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs529077777	chr11:67239795-67239796	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs551091842	chr11:67239796-67239797	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs59916629	chr11:67239799-67239800	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs193087423	chr11:67239813-67239814	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs535804318	chr11:67239851-67239852	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs547830355	chr11:67239865-67239866	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs566152706	chr11:67239875-67239876	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs557393979	chr11:67239885-67239886	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs185332778	chr11:67240000-67240001	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs558372275	chr11:67240002-67240003	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs576621168	chr11:67240005-67240006	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pituitary adenoma	20530095	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67237200-67238800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr11:67237200-67241800	Weak transcription	Liver	Liver
3	chr11:67237200-67249200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:67237200-67250200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr11:67237400-67239000	Enhancers	GM12878-XiMat	blood
6	chr11:67237400-67239400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr11:67237800-67249800	Weak transcription	Lung	lung
8	chr11:67238200-67239200	Enhancers	HepG2	liver
9	chr11:67238400-67239200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:67238400-67249800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:67238800-67239000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:67238800-67239000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:67238800-67239400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr11:67239200-67239400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:67239400-67240600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr11:67240200-67240400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr11:67240400-67242600	Enhancers	HepG2	liver
18	chr11:67241800-67242600	Enhancers	Liver	Liver
19	chr11:67242600-67244200	Weak transcription	HepG2	liver
20	chr11:67242600-67249600	Weak transcription	Liver	Liver
21	chr11:67244200-67244400	Enhancers	K562	blood
22	chr11:67244200-67245800	Enhancers	HepG2	liver
23	chr11:67244400-67244800	Flanking Active TSS	K562	blood
24	chr11:67244600-67249600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr11:67244800-67245800	Enhancers	K562	blood
26	chr11:67245800-67249200	Weak transcription	K562	blood
27	chr11:67245800-67249600	Weak transcription	HepG2	liver
28	chr11:67249200-67249400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr11:67249200-67249800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr11:67249200-67249800	Enhancers	Primary T cells fromperipheralblood	blood
31	chr11:67249200-67249800	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr11:67249200-67249800	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr11:67249200-67249800	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr11:67249200-67249800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr11:67249200-67249800	Enhancers	K562	blood
36	chr11:67249200-67250200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr11:67249200-67250800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:67249400-67249600	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr11:67249400-67249800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:67249400-67249800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr11:67249400-67249800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr11:67249600-67249800	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr11:67249600-67249800	Enhancers	Primary B cells from cord blood	blood
44	chr11:67249600-67249800	Enhancers	Primary B cells from peripheral blood	blood
45	chr11:67249600-67249800	Enhancers	Primary T cells from cord blood	blood
46	chr11:67249600-67249800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr11:67249600-67249800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr11:67249600-67249800	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr11:67249600-67249800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:67249600-67249800	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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