Variant report

Variant	nsv556471
Chromosome Location	chr11:119564496-119588062
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:561)
CpG islands
(count:183)
Chromatin interactive
region (count:40)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:119571750-119571826	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:119565174-119565520	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:119583956-119584217	HepG2	liver:	n/a	n/a
4	BHLHE40	chr11:119575730-119575892	K562	blood:	n/a	n/a
5	BHLHE40	chr11:119582344-119582472	HepG2	liver:	n/a	n/a
6	BHLHE40	chr11:119565095-119565422	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:119565145-119565519	HepG2	liver:	n/a	n/a
8	BHLHE40	chr11:119587487-119587595	K562	blood:	n/a	n/a
9	BHLHE40	chr11:119583141-119583277	HepG2	liver:	n/a	n/a
10	BHLHE40	chr11:119583485-119583580	K562	blood:	n/a	chr11:119583531-119583552
11	BRCA1	chr11:119565203-119565421	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:119565188-119565528	HepG2	liver:	n/a	n/a
13	CEBPB	chr11:119571264-119571735	HepG2	liver:	n/a	chr11:119571411-119571422
14	CEBPD	chr11:119575591-119575958	K562	blood:	n/a	n/a
15	CHD2	chr11:119580594-119580917	GM12878	blood:	n/a	n/a
16	CHD2	chr11:119567069-119567269	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr11:119585176-119585191	HepG2	liver:	n/a	n/a
18	CTCF	chr11:119587280-119587430	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr11:119577720-119577870	HRPEpiC	eye:	n/a	chr11:119577791-119577800
20	CTCF	chr11:119577760-119577910	GM12865	blood:	n/a	chr11:119577791-119577800
21	CTCF	chr11:119577740-119577890	GM12873	blood:	n/a	chr11:119577791-119577800
22	CTCF	chr11:119565220-119565370	HL-60	blood:	n/a	chr11:119565322-119565340
23	CTCF	chr11:119565060-119565350	GM12870	blood:	n/a	chr11:119565322-119565340
24	CTCF	chr11:119565260-119565410	GM12865	blood:	n/a	chr11:119565322-119565340
25	CTCF	chr11:119577740-119577890	HL-60	blood:	n/a	chr11:119577791-119577800
26	CTCF	chr11:119587166-119587562	K562	blood:	n/a	n/a
27	CTCF	chr11:119565240-119565390	GM12878	blood:	n/a	chr11:119565322-119565340
28	CTCF	chr11:119577820-119577970	NB4	blood:	n/a	n/a
29	CTCF	chr11:119565229-119565427	GM12878	blood:	n/a	chr11:119565322-119565340
30	CTCF	chr11:119567480-119567630	SAEC	small airway:	n/a	n/a
31	CTCF	chr11:119565160-119565310	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr11:119572774-119572910	MCF-7	breast:	n/a	chr11:119572801-119572814
33	CTCF	chr11:119577740-119577890	Caco-2	colon:	n/a	chr11:119577791-119577800
34	CTCF	chr11:119565300-119565450	GM06990	blood:	n/a	chr11:119565322-119565340
35	CTCF	chr11:119577700-119577850	Hela-S3	cervix:	n/a	chr11:119577791-119577800
36	CTCF	chr11:119577720-119577870	HPF	lung:	n/a	chr11:119577791-119577800
37	CTCF	chr11:119565259-119565422	A549	lung:	n/a	chr11:119565322-119565340
38	CTCF	chr11:119565200-119565350	HUVEC	blood vessel:	n/a	chr11:119565322-119565340
39	CTCF	chr11:119572760-119572889	MCF-7	breast:	n/a	chr11:119572801-119572814
40	CTCF	chr11:119577675-119577882	HepG2	liver:	n/a	chr11:119577791-119577800
41	CTCF	chr11:119577820-119577970	GM12873	blood:	n/a	n/a
42	CTCF	chr11:119577720-119577870	HCPEpiC	choroid plexus:	n/a	chr11:119577791-119577800
43	CTCF	chr11:119565211-119565426	MCF-7	breast:	n/a	chr11:119565322-119565340
44	CTCF	chr11:119577717-119577892	HUVEC	blood vessel:	n/a	chr11:119577791-119577800
45	CTCF	chr11:119577800-119577950	GM06990	blood:	n/a	n/a
46	CTCF	chr11:119577700-119577850	MCF-7	breast:	n/a	chr11:119577791-119577800
47	CTCF	chr11:119565559-119565566	GM19239	blood:	n/a	n/a
48	CTCF	chr11:119587300-119587450	AG04450	lung:	n/a	n/a
49	CTCF	chr11:119565260-119565410	GM12869	blood:	n/a	chr11:119565322-119565340
50	CTCF	chr11:119565227-119565435	HepG2	liver:	n/a	chr11:119565322-119565340

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:119587364-119587414	H1-hESC	embryonic stem cell:	embryo
2	chr11:119567761-119567811	ECC-1	luminal epithelium:	n/a
3	chr11:119580588-119580638	HCF	heart:	n/a
4	chr11:119580588-119580638	SAEC	small airway:	n/a
5	chr11:119580588-119580638	GM12892	blood:	n/a
6	chr11:119587364-119587414	HRPEpiC	eye:	n/a
7	chr11:119567761-119567811	HCT-116	colon:	n/a
8	chr11:119580588-119580638	HMEC	breast:	n/a
9	chr11:119567761-119567811	NT2-D1	testis:	n/a
10	chr11:119567761-119567811	HEK293	kidney:	embryo
11	chr11:119567761-119567811	BJ	skin:	n/a
12	chr11:119580588-119580638	GM06990	blood:	n/a
13	chr11:119567761-119567811	HEEpiC	esophagus:	n/a
14	chr11:119580588-119580638	ProgFib	skin:	n/a
15	chr11:119580588-119580638	HEEpiC	esophagus:	n/a
16	chr11:119587364-119587414	PFSK-1	brain:	n/a
17	chr11:119580588-119580638	HRE	kidney:	n/a
18	chr11:119580588-119580638	HAEpiC	amniotic membrane:	n/a
19	chr11:119580588-119580638	CMK	blood:	n/a
20	chr11:119567761-119567811	NB4	blood:	n/a
21	chr11:119587364-119587414	SKMC	muscle:	n/a
22	chr11:119587364-119587414	HL-60	blood:	n/a
23	chr11:119587364-119587414	HRCEpiC	kidney:	n/a
24	chr11:119567761-119567811	HUVEC	blood vessel:	n/a
25	chr11:119567761-119567811	A549	lung:	n/a
26	chr11:119587364-119587414	LNCaP	prostate:	n/a
27	chr11:119580588-119580638	AG09319	gingival:	n/a
28	chr11:119587364-119587414	ovcar-3	ovarian:	n/a
29	chr11:119587364-119587414	GM12891	blood:	n/a
30	chr11:119587364-119587414	GM19239	blood:	n/a
31	chr11:119580588-119580638	NHBE	bronchial:	n/a
32	chr11:119587364-119587414	AG04450	lung:	fetal
33	chr11:119567761-119567811	NHDF-neo	bronchial:	n/a
34	chr11:119567761-119567811	HAEpiC	amniotic membrane:	n/a
35	chr11:119587364-119587414	AG09319	gingival:	n/a
36	chr11:119580588-119580638	BJ	skin:	n/a
37	chr11:119580588-119580638	T-47D	breast:	n/a
38	chr11:119567761-119567811	Hepatocyte	liver:	n/a
39	chr11:119580588-119580638	AG04450	lung:	fetal
40	chr11:119580588-119580638	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:119587364-119587414	GM06990	blood:	n/a
42	chr11:119580588-119580638	H1-hESC	embryonic stem cell:	embryo
43	chr11:119567761-119567811	HNPCEpiC	eye:	n/a
44	chr11:119567761-119567811	SAEC	small airway:	n/a
45	chr11:119580588-119580638	PFSK-1	brain:	n/a
46	chr11:119567761-119567811	GM06990	blood:	n/a
47	chr11:119587364-119587414	PrEC	prostate:	n/a
48	chr11:119580588-119580638	BE2_C	brain:	n/a
49	chr11:119567761-119567811	AG09319	gingival:	n/a
50	chr11:119587364-119587414	ECC-1	luminal epithelium:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:119558592..119561187-chr11:119565214..119567507,2	MCF-7	breast:
2	chr11:119568263..119570489-chr11:119571275..119572812,2	K562	blood:
3	chr11:119576493..119579043-chr11:119584398..119586423,2	MCF-7	breast:
4	chr11:119579836..119582330-chr11:119583549..119585842,2	MCF-7	breast:
5	chr11:119573833..119575593-chr11:119596790..119599560,2	MCF-7	breast:
6	chr11:119554561..119556794-chr11:119570560..119572885,2	MCF-7	breast:
7	chr11:119571255..119574750-chr11:119575063..119576895,3	MCF-7	breast:
8	chr11:119582567..119584889-chr11:119586809..119588418,2	MCF-7	breast:
9	chr11:119581664..119584119-chr11:119591435..119593140,2	MCF-7	breast:
10	chr11:119556235..119560513-chr11:119562313..119564680,4	K562	blood:
11	chr11:119582567..119584889-chr11:119586809..119588418,2	MCF-7	breast:
12	chr11:119568716..119570438-chr11:119574032..119575735,2	MCF-7	breast:
13	chr11:119568589..119571498-chr11:119574354..119576763,2	MCF-7	breast:
14	chr11:119561073..119563172-chr11:119565321..119568250,2	K562	blood:
15	chr11:119546001..119548946-chr11:119570439..119572387,2	MCF-7	breast:
16	chr11:119553834..119555975-chr11:119568134..119570409,2	MCF-7	breast:
17	chr11:119572643..119574728-chr11:119576925..119579390,2	MCF-7	breast:
18	chr11:119556235..119559099-chr11:119563178..119564680,2	K562	blood:
19	chr11:119567595..119569306-chr11:119571218..119572844,2	MCF-7	breast:
20	chr11:119568263..119570489-chr11:119571275..119572812,2	K562	blood:
21	chr11:119564818..119565650-chr11:119598208..119598847,2	MCF-7	breast:
22	chr11:119568098..119571267-chr11:119595317..119602165,10	MCF-7	breast:
23	chr11:119572643..119574728-chr11:119576925..119579390,2	MCF-7	breast:
24	chr11:119586160..119588089-chr11:119597463..119599607,2	MCF-7	breast:
25	chr11:119578331..119580613-chr11:119597735..119601327,3	MCF-7	breast:
26	chr11:119563935..119565490-chr11:119599078..119601378,2	MCF-7	breast:
27	chr11:119565895..119567556-chr11:119593844..119596406,2	MCF-7	breast:
28	chr11:119568589..119571498-chr11:119574354..119576763,2	MCF-7	breast:
29	chr11:119576493..119579043-chr11:119584398..119586423,2	MCF-7	breast:
30	chr11:119582343..119585155-chr11:119589653..119593219,3	MCF-7	breast:
31	chr11:119571255..119574750-chr11:119575063..119576895,3	MCF-7	breast:
32	chr11:119561359..119563599-chr11:119570255..119571810,2	K562	blood:
33	chr11:119568716..119570438-chr11:119574032..119575735,2	MCF-7	breast:
34	chr11:119563899..119565883-chr11:119570340..119572500,2	MCF-7	breast:
35	chr11:119586554..119590249-chr11:119604143..119607234,3	K562	blood:
36	chr11:119551416..119553458-chr11:119566192..119569088,2	MCF-7	breast:
37	chr11:119587850..119589350-chr11:119589562..119592404,2	MCF-7	breast:
38	chr11:119563899..119565883-chr11:119570340..119572500,2	MCF-7	breast:
39	chr11:119536890..119537510-chr11:119583273..119583779,2	MCF-7	breast:
40	chr11:119567595..119569306-chr11:119571218..119572844,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2523D13.1.1-6	chr11:119583602-119583722	ENSG00000255247.1
2	lnc-CTD-2523D13.1.1-6	chr11:119584309-119584635	ENSG00000255247.1
3	lnc-CTD-2523D13.1.1-6	chr11:119580630-119580740	ENSG00000255247.1

No data

Variant related genes	Relation type
ENSG00000255247	TF binding region
ENSG00000255247	CpG island
ENSG00000255247	chromatin interactions
ENSG00000110400	chromatin interactions
ENSG00000254854	chromatin interactions

Extended variants
information (count: 933 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11217409	chr11:119564496-119564497	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74573766	chr11:119564516-119564517	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs140186337	chr11:119564528-119564529	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs11217410	chr11:119564536-119564537	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs568590399	chr11:119564570-119564571	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs529373156	chr11:119564599-119564600	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs547484505	chr11:119564600-119564601	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs566019564	chr11:119564613-119564614	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs539448078	chr11:119564641-119564642	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs34393167	chr11:119564685-119564686	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs558472856	chr11:119564714-119564715	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570240651	chr11:119564720-119564721	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs537273915	chr11:119564723-119564724	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs7124922	chr11:119564735-119564736	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs574208870	chr11:119564746-119564747	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs7124934	chr11:119564781-119564782	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs553490331	chr11:119564824-119564825	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs7110874	chr11:119564842-119564843	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs545472182	chr11:119564874-119564875	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564438526	chr11:119564900-119564901	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs78280378	chr11:119564908-119564909	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs548787718	chr11:119564944-119564945	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs181834776	chr11:119564947-119564948	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs529410420	chr11:119564948-119564949	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs377625189	chr11:119564964-119564965	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs566032779	chr11:119564987-119564988	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs533401547	chr11:119565035-119565036	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs79289906	chr11:119565041-119565042	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs570032830	chr11:119565092-119565093	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546537157	chr11:119565093-119565094	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537310750	chr11:119565094-119565095	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571196903	chr11:119565150-119565151	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549173224	chr11:119565177-119565178	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs538933505	chr11:119565198-119565199	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs567471645	chr11:119565202-119565203	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552993419	chr11:119565222-119565223	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs534884216	chr11:119565244-119565245	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553870556	chr11:119565298-119565299	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs572030321	chr11:119565319-119565320	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs56379168	chr11:119565364-119565365	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539446754	chr11:119565406-119565407	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs557435456	chr11:119565461-119565462	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs183679745	chr11:119565466-119565467	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs543696126	chr11:119565480-119565481	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561962540	chr11:119565489-119565490	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs7950059	chr11:119565495-119565496	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs188048422	chr11:119565534-119565535	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377524559	chr11:119565535-119565536	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370929320	chr11:119565595-119565596	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533238627	chr11:119565626-119565627	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	17142309	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119550200-119567400	Enhancers	Esophagus	oesophagus
2	chr11:119551600-119567400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:119553800-119565200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr11:119554600-119566400	Enhancers	Fetal Muscle Leg	muscle
5	chr11:119555800-119568800	Weak transcription	Left Ventricle	heart
6	chr11:119556000-119568600	Weak transcription	Right Atrium	heart
7	chr11:119556000-119571600	Weak transcription	NHLF	lung
8	chr11:119556600-119564800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr11:119556600-119565200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:119559000-119567200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:119559400-119566200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr11:119559800-119570200	Enhancers	Fetal Thymus	thymus
13	chr11:119560400-119566400	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr11:119560400-119567800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:119560400-119569600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr11:119561000-119565600	Enhancers	Thymus	Thymus
17	chr11:119561000-119580600	Weak transcription	Fetal Kidney	kidney
18	chr11:119561200-119567800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:119561400-119565400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:119561400-119565400	Enhancers	Brain Germinal Matrix	brain
21	chr11:119561400-119566400	Enhancers	Primary hematopoietic stem cells	blood
22	chr11:119561400-119568800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr11:119561600-119565600	Enhancers	GM12878-XiMat	blood
24	chr11:119561800-119564600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:119561800-119565200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr11:119561800-119565200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr11:119561800-119566400	Enhancers	Brain Angular Gyrus	brain
28	chr11:119561800-119566400	Enhancers	Brain Cingulate Gyrus	brain
29	chr11:119561800-119568400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr11:119561800-119568800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr11:119561800-119577600	Enhancers	Brain Hippocampus Middle	brain
32	chr11:119562000-119564600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr11:119562000-119565400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr11:119562000-119565800	Enhancers	Brain Anterior Caudate	brain
35	chr11:119562000-119566400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr11:119562000-119568600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr11:119562000-119578400	Enhancers	Duodenum Mucosa	Duodenum
38	chr11:119562200-119564600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:119562200-119564600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr11:119562200-119564600	Enhancers	Fetal Brain Male	brain
41	chr11:119562200-119565200	Weak transcription	Primary B cells from cord blood	blood
42	chr11:119562200-119566600	Enhancers	Brain Substantia Nigra	brain
43	chr11:119562400-119564800	Weak transcription	Adipose Nuclei	Adipose
44	chr11:119562400-119564800	Weak transcription	HepG2	liver
45	chr11:119562400-119565200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr11:119562400-119571000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:119562400-119571000	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr11:119562600-119565800	Enhancers	Pancreas	Pancrea
49	chr11:119563000-119564800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr11:119563000-119567400	Weak transcription	Right Ventricle	heart

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