Variant report

Variant	esv1793754
Chromosome Location	chr11:72335673-72348106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:203)
CpG islands
(count:183)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:72343646-72343697	K562	blood:	n/a	n/a
2	ATF1	chr11:72337570-72337657	K562	blood:	n/a	n/a
3	ATF1	chr11:72343454-72343810	K562	blood:	n/a	n/a
4	BCL3	chr11:72335279-72336043	GM12878	blood:	n/a	n/a
5	BCL3	chr11:72335513-72336001	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:72341243-72341485	K562	blood:	n/a	chr11:72341331-72341352 chr11:72341337-72341346 chr11:72341337-72341346 chr11:72341336-72341345 chr11:72341335-72341348
7	BHLHE40	chr11:72336842-72336909	K562	blood:	n/a	n/a
8	BHLHE40	chr11:72335523-72335833	K562	blood:	n/a	n/a
9	BHLHE40	chr11:72343412-72343769	K562	blood:	n/a	n/a
10	BHLHE40	chr11:72337488-72337642	K562	blood:	n/a	n/a
11	CBX3	chr11:72343218-72343905	K562	blood:	n/a	n/a
12	CCNT2	chr11:72336862-72337135	K562	blood:	n/a	chr11:72336996-72337005
13	CCNT2	chr11:72343476-72343734	K562	blood:	n/a	n/a
14	CEBPB	chr11:72346666-72346832	K562	blood:	n/a	n/a
15	CEBPB	chr11:72343602-72343609	K562	blood:	n/a	n/a
16	CEBPB	chr11:72336888-72337062	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:72346716-72346886	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:72346758-72346831	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:72346617-72346917	K562	blood:	n/a	n/a
20	CHD2	chr11:72336983-72337139	HepG2	liver:	n/a	n/a
21	CTCF	chr11:72340880-72341030	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr11:72340620-72340770	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr11:72340820-72340970	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr11:72335665-72335848	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr11:72341380-72341530	Caco-2	colon:	n/a	n/a
26	CTCF	chr11:72346550-72346572	GM10248	blood:	n/a	n/a
27	CTCF	chr11:72340942-72340947	K562	blood:	n/a	n/a
28	CTCF	chr11:72340871-72340957	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr11:72340960-72341110	GM12874	blood:	n/a	n/a
30	CTCF	chr11:72340878-72340930	K562	blood:	n/a	n/a
31	CTCF	chr11:72347140-72347290	HCPEpiC	choroid plexus:	n/a	chr11:72347240-72347253
32	CTCF	chr11:72335713-72335793	K562	blood:	n/a	n/a
33	CTCF	chr11:72341680-72341830	HBMEC	blood vessel:	n/a	n/a
34	E2F6	chr11:72341591-72341763	K562	blood:	n/a	n/a
35	E2F6	chr11:72343244-72343691	K562	blood:	n/a	n/a
36	EBF1	chr11:72341714-72341774	GM12878	blood:	n/a	chr11:72341748-72341759
37	EGR1	chr11:72337574-72337773	K562	blood:	n/a	n/a
38	EGR1	chr11:72343444-72343958	K562	blood:	n/a	n/a
39	EGR1	chr11:72343565-72343855	K562	blood:	n/a	n/a
40	ELF1	chr11:72336707-72337020	K562	blood:	n/a	n/a
41	ELF1	chr11:72343403-72343813	K562	blood:	n/a	n/a
42	EP300	chr11:72343380-72343854	K562	blood:	n/a	n/a
43	EP300	chr11:72342301-72344837	SK-N-SH	brain:	n/a	chr11:72344071-72344087 chr11:72342868-72342884
44	EP300	chr11:72340395-72340701	SK-N-SH_RA	brain:	n/a	chr11:72340623-72340639
45	EP300	chr11:72339830-72341173	SK-N-SH	brain:	n/a	chr11:72340623-72340639
46	EP300	chr11:72344213-72344239	K562	blood:	n/a	n/a
47	EP300	chr11:72340417-72340643	SK-N-SH_RA	brain:	n/a	chr11:72340623-72340639
48	ETS1	chr11:72343416-72343709	K562	blood:	n/a	n/a
49	FOS	chr11:72343283-72343835	HUVEC	blood vessel:	n/a	n/a
50	FOS	chr11:72335714-72336100	HUVEC	blood vessel:	n/a	chr11:72335870-72335881 chr11:72335872-72335881

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:72343473-72343523	PANC-1	pancreas:	n/a
2	chr11:72336908-72336958	GM12892	blood:	n/a
3	chr11:72343473-72343523	ECC-1	luminal epithelium:	n/a
4	chr11:72347339-72347389	MCF-7	breast:	n/a
5	chr11:72343473-72343523	CMK	blood:	n/a
6	chr11:72347339-72347389	ECC-1	luminal epithelium:	n/a
7	chr11:72336908-72336958	SK-N-SH_RA	brain:	n/a
8	chr11:72347339-72347389	AG09309	skin:	n/a
9	chr11:72343473-72343523	NHBE	bronchial:	n/a
10	chr11:72336908-72336958	HCPEpiC	choroid plexus:	n/a
11	chr11:72336908-72336958	IMR90	lung:	fetal
12	chr11:72347339-72347389	HRCEpiC	kidney:	n/a
13	chr11:72347339-72347389	GM12891	blood:	n/a
14	chr11:72347339-72347389	GM12878	blood:	n/a
15	chr11:72336908-72336958	ProgFib	skin:	n/a
16	chr11:72336908-72336958	NHBE	bronchial:	n/a
17	chr11:72336908-72336958	Hela-S3	cervix:	n/a
18	chr11:72347339-72347389	HCT-116	colon:	n/a
19	chr11:72347339-72347389	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:72347339-72347389	LNCaP	prostate:	n/a
21	chr11:72343473-72343523	HNPCEpiC	eye:	n/a
22	chr11:72336908-72336958	PFSK-1	brain:	n/a
23	chr11:72343473-72343523	SAEC	small airway:	n/a
24	chr11:72343473-72343523	NT2-D1	testis:	n/a
25	chr11:72336908-72336958	K562	blood:	n/a
26	chr11:72336908-72336958	GM19239	blood:	n/a
27	chr11:72347339-72347389	GM19239	blood:	n/a
28	chr11:72343473-72343523	H1-hESC	embryonic stem cell:	embryo
29	chr11:72343473-72343523	SK-N-SH_RA	brain:	n/a
30	chr11:72343473-72343523	HUVEC	blood vessel:	n/a
31	chr11:72343473-72343523	PrEC	prostate:	n/a
32	chr11:72336908-72336958	GM12878	blood:	n/a
33	chr11:72347339-72347389	AoSMC	blood vessel:	n/a
34	chr11:72343473-72343523	HepG2	liver:	n/a
35	chr11:72343473-72343523	Caco-2	colon:	n/a
36	chr11:72336908-72336958	Hepatocyte	liver:	n/a
37	chr11:72347339-72347389	U87	brain:	n/a
38	chr11:72336908-72336958	AoSMC	blood vessel:	n/a
39	chr11:72347339-72347389	AG04449	skin:	fetal
40	chr11:72343473-72343523	MCF10A-Er-Src	breast:	n/a
41	chr11:72336908-72336958	A549	lung:	n/a
42	chr11:72336908-72336958	GM12891	blood:	n/a
43	chr11:72343473-72343523	AG04450	lung:	fetal
44	chr11:72347339-72347389	Jurkat	blood:	n/a
45	chr11:72343473-72343523	GM12892	blood:	n/a
46	chr11:72343473-72343523	AoSMC	blood vessel:	n/a
47	chr11:72347339-72347389	HCPEpiC	choroid plexus:	n/a
48	chr11:72336908-72336958	HCF	heart:	n/a
49	chr11:72336908-72336958	CMK	blood:	n/a
50	chr11:72336908-72336958	NH-A	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:72329305..72334052-chr11:72334284..72337478,5	K562	blood:
2	chr11:72343339..72345279-chr11:72353249..72356170,2	K562	blood:
3	chr11:71930243..71933219-chr11:72343934..72345638,2	K562	blood:
4	chr11:72339617..72343114-chr11:72344003..72346053,4	K562	blood:
5	chr11:72332869..72335160-chr11:72338112..72340780,2	K562	blood:
6	chr11:72333492..72335782-chr11:72342126..72344876,2	K562	blood:
7	chr11:72324405..72326702-chr11:72335643..72338443,2	K562	blood:
8	chr11:72336037..72338838-chr11:72339942..72342746,4	K562	blood:
9	chr11:72321045..72323854-chr11:72340699..72343138,2	K562	blood:
10	chr11:72338376..72339958-chr11:72347160..72349591,2	K562	blood:
11	chr11:72342072..72343913-chr11:72348665..72350291,3	K562	blood:
12	chr11:72334834..72339078-chr11:72340923..72346253,6	K562	blood:
13	chr11:72321761..72324145-chr11:72337508..72339149,2	K562	blood:
14	chr11:72341496..72343582-chr11:72364594..72367336,2	MCF-7	breast:
15	chr11:72339617..72343114-chr11:72344003..72346053,4	K562	blood:
16	chr11:72334834..72339078-chr11:72340923..72346253,6	K562	blood:
17	chr11:72341497..72343932-chr11:72350783..72352444,2	K562	blood:
18	chr11:72310660..72312266-chr11:72342413..72344790,2	MCF-7	breast:
19	chr11:72309197..72311837-chr11:72341889..72344712,2	K562	blood:
20	chr11:72303390..72305679-chr11:72341481..72343396,2	K562	blood:
21	chr11:72325202..72330805-chr11:72334238..72338443,6	K562	blood:
22	chr11:72342508..72344347-chr11:72346096..72348367,4	K562	blood:
23	chr11:72333492..72335782-chr11:72342126..72344876,2	K562	blood:
24	chr11:72313089..72314978-chr11:72334364..72335937,2	K562	blood:
25	chr11:72335997..72337699-chr11:72363120..72365299,2	K562	blood:
26	chr11:72324136..72326937-chr11:72343059..72344870,2	K562	blood:
27	chr11:72336037..72338838-chr11:72339942..72342746,4	K562	blood:
28	chr11:72340095..72342278-chr11:72348258..72351014,2	MCF-7	breast:
29	chr11:72311450..72313060-chr11:72334269..72335781,2	K562	blood:
30	chr11:72340350..72342002-chr11:72346952..72349223,2	MCF-7	breast:

No data

Variant related genes	Relation type
PDE2A	TF binding region
PDE2A	CpG island
ENSG00000186642	chromatin interactions
ENSG00000251919	chromatin interactions
ENSG00000272036	chromatin interactions
ENSG00000255808	chromatin interactions

Extended variants
information (count: 521 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139033790	chr11:72335708-72335709	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs552987042	chr11:72335717-72335718	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs574373842	chr11:72335730-72335731	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs11235552	chr11:72335731-72335732	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558075466	chr11:72335737-72335738	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs377767163	chr11:72335796-72335797	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs200005004	chr11:72335814-72335815	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs459309	chr11:72335834-72335835	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs543529883	chr11:72335840-72335841	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs561724947	chr11:72335842-72335843	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs529283291	chr11:72335928-72335929	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373721350	chr11:72335935-72335936	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143775270	chr11:72335961-72335962	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533087007	chr11:72335998-72335999	Weak transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs460633	chr11:72336021-72336022	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569775230	chr11:72336030-72336031	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs115820022	chr11:72336051-72336052	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549136139	chr11:72336056-72336057	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs567263702	chr11:72336079-72336080	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs534648768	chr11:72336103-72336104	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs76723921	chr11:72336142-72336143	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575748406	chr11:72336189-72336190	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs553005446	chr11:72336213-72336214	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs78923661	chr11:72336215-72336216	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116675277	chr11:72336247-72336248	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs7123699	chr11:72336248-72336249	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs148248056	chr11:72336289-72336290	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543495331	chr11:72336298-72336299	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs555481403	chr11:72336322-72336323	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573799920	chr11:72336354-72336355	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs540987538	chr11:72336373-72336374	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs7123937	chr11:72336375-72336376	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564380767	chr11:72336446-72336447	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs553113640	chr11:72336447-72336448	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs533229385	chr11:72336475-72336476	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs113977668	chr11:72336502-72336503	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs370812607	chr11:72336530-72336531	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs366068	chr11:72336564-72336565	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs530769526	chr11:72336568-72336569	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs76914878	chr11:72336619-72336620	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs188794360	chr11:72336630-72336631	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs150749729	chr11:72336639-72336640	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs137955811	chr11:72336678-72336679	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs401999	chr11:72336693-72336694	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs115806600	chr11:72336694-72336695	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs192515824	chr11:72336706-72336707	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570221811	chr11:72336725-72336726	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs2047506	chr11:72336831-72336832	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs75371948	chr11:72336833-72336834	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573763700	chr11:72336836-72336837	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	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
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72329400-72335800	Weak transcription	Brain Hippocampus Middle	brain
2	chr11:72329600-72336000	Weak transcription	Brain Germinal Matrix	brain
3	chr11:72330600-72335800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr11:72330600-72336200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr11:72331400-72335800	Weak transcription	Fetal Brain Male	brain
6	chr11:72331400-72341200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:72331600-72336800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr11:72332200-72336000	Weak transcription	Fetal Stomach	stomach
9	chr11:72332200-72336200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:72333600-72335800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr11:72334200-72341600	Enhancers	Right Atrium	heart
12	chr11:72334400-72338800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr11:72334800-72350200	Enhancers	Left Ventricle	heart
14	chr11:72335400-72335800	Enhancers	Fetal Kidney	kidney
15	chr11:72335400-72336000	Genic enhancers	Duodenum Mucosa	Duodenum
16	chr11:72335400-72336000	Genic enhancers	Stomach Smooth Muscle	stomach
17	chr11:72335400-72336000	Enhancers	Spleen	Spleen
18	chr11:72335400-72337200	Enhancers	Primary hematopoietic stem cells	blood
19	chr11:72335400-72337800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:72335400-72337800	Enhancers	Gastric	stomach
21	chr11:72335400-72338000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:72335400-72338000	Enhancers	Fetal Intestine Small	intestine
23	chr11:72335400-72338400	Enhancers	HUVEC	blood vessel
24	chr11:72335400-72340000	Enhancers	Fetal Brain Female	brain
25	chr11:72335400-72340200	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr11:72335400-72341200	Enhancers	Brain Anterior Caudate	brain
27	chr11:72335400-72346600	Enhancers	Brain Angular Gyrus	brain
28	chr11:72335600-72335800	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:72335600-72335800	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr11:72335600-72336000	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:72335600-72336200	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr11:72335600-72336200	Bivalent Enhancer	HepG2	liver
33	chr11:72335600-72336200	Bivalent Enhancer	NHDF-Ad	bronchial
34	chr11:72335600-72336400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
35	chr11:72335600-72337400	Enhancers	Pancreas	Pancrea
36	chr11:72335600-72338000	Enhancers	Stomach Mucosa	stomach
37	chr11:72335600-72338200	Enhancers	Brain Cingulate Gyrus	brain
38	chr11:72335600-72338200	Enhancers	K562	blood
39	chr11:72335600-72338400	Enhancers	Fetal Lung	lung
40	chr11:72335600-72338800	Enhancers	Esophagus	oesophagus
41	chr11:72335600-72340800	Enhancers	Colon Smooth Muscle	Colon
42	chr11:72335600-72341000	Enhancers	Right Ventricle	heart
43	chr11:72335600-72341200	Enhancers	Brain Substantia Nigra	brain
44	chr11:72335600-72341200	Enhancers	Lung	lung
45	chr11:72335600-72344600	Enhancers	Rectal Smooth Muscle	rectum
46	chr11:72335600-72349400	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr11:72335800-72336200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr11:72335800-72336400	Enhancers	Adipose Nuclei	Adipose
49	chr11:72335800-72337600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr11:72335800-72337800	Enhancers	Rectal Mucosa Donor 31	rectum

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