Variant report

Variant	nsv1045130
Chromosome Location	chr11:34641598-34777725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2444)
CpG islands
(count:794)
Chromatin interactive
region (count:100)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34664524-34664676	K562	blood:	n/a	n/a
2	ARID3A	chr11:34686478-34687268	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:34706908-34707346	K562	blood:	n/a	n/a
4	ARID3A	chr11:34707057-34707061	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:34748846-34749059	K562	blood:	n/a	n/a
6	ARID3A	chr11:34655611-34656115	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:34673150-34674076	K562	blood:	n/a	n/a
8	ARID3A	chr11:34661875-34662144	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:34689665-34690249	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:34675333-34678461	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:34667925-34667948	K562	blood:	n/a	n/a
12	ATF1	chr11:34748782-34749093	K562	blood:	n/a	n/a
13	ATF1	chr11:34687084-34687254	K562	blood:	n/a	n/a
14	ATF1	chr11:34706870-34707207	K562	blood:	n/a	n/a
15	ATF1	chr11:34675550-34675863	K562	blood:	n/a	n/a
16	ATF1	chr11:34673739-34674051	K562	blood:	n/a	n/a
17	ATF2	chr11:34655408-34656051	GM12878	blood:	n/a	n/a
18	ATF2	chr11:34671884-34672577	GM12878	blood:	n/a	n/a
19	ATF2	chr11:34706715-34707242	GM12878	blood:	n/a	n/a
20	ATF2	chr11:34671847-34672599	GM12878	blood:	n/a	n/a
21	ATF2	chr11:34706739-34707148	GM12878	blood:	n/a	n/a
22	ATF2	chr11:34673623-34674581	GM12878	blood:	n/a	n/a
23	ATF2	chr11:34644852-34645273	GM12878	blood:	n/a	n/a
24	ATF3	chr11:34673654-34674049	K562	blood:	n/a	n/a
25	ATF3	chr11:34706580-34707376	HCT-116	colon:	n/a	n/a
26	ATF3	chr11:34661628-34662235	A549	lung:	n/a	n/a
27	ATF3	chr11:34661411-34662279	A549	lung:	n/a	n/a
28	ATF3	chr11:34676265-34676876	A549	lung:	n/a	n/a
29	ATF3	chr11:34706702-34707206	K562	blood:	n/a	n/a
30	ATF3	chr11:34706701-34707439	HCT-116	colon:	n/a	n/a
31	ATF3	chr11:34676387-34677171	A549	lung:	n/a	n/a
32	ATF3	chr11:34675433-34676137	A549	lung:	n/a	n/a
33	ATF3	chr11:34706685-34707409	A549	lung:	n/a	n/a
34	ATF3	chr11:34675408-34676126	A549	lung:	n/a	n/a
35	ATF3	chr11:34706711-34707373	A549	lung:	n/a	n/a
36	BACH1	chr11:34706943-34706985	K562	blood:	n/a	chr11:34706944-34706958
37	BACH1	chr11:34706823-34707127	H1-hESC	embryonic stem cell:	n/a	chr11:34706944-34706958
38	BATF	chr11:34672024-34672548	GM12878	blood:	n/a	n/a
39	BATF	chr11:34706746-34707114	GM12878	blood:	n/a	chr11:34706944-34706954 chr11:34706943-34706954
40	BATF	chr11:34673744-34674060	GM12878	blood:	n/a	n/a
41	BATF	chr11:34644902-34645267	GM12878	blood:	n/a	n/a
42	BATF	chr11:34647977-34648245	GM12878	blood:	n/a	n/a
43	BATF	chr11:34655400-34656160	GM12878	blood:	n/a	n/a
44	BATF	chr11:34672082-34672559	GM12878	blood:	n/a	n/a
45	BATF	chr11:34655552-34655984	GM12878	blood:	n/a	n/a
46	BATF	chr11:34645527-34645908	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:34672057-34672482	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:34655659-34656004	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:34671993-34672559	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:34655737-34656027	GM12878	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34672025-34672075	LNCaP	prostate:	n/a
2	chr11:34672025-34672075	LNCaP	prostate:	n/a
3	chr11:34672025-34672075	A549	lung:	n/a
4	chr11:34681375-34681425	BJ	skin:	n/a
5	chr11:34642463-34642513	A549	lung:	n/a
6	chr11:34666060-34666110	HMEC	breast:	n/a
7	chr11:34654233-34654283	HAEpiC	amniotic membrane:	n/a
8	chr11:34641925-34641975	HL-60	blood:	n/a
9	chr11:34701819-34701869	HRPEpiC	eye:	n/a
10	chr11:34654233-34654283	SK-N-SH	brain:	n/a
11	chr11:34642885-34642935	GM12891	blood:	n/a
12	chr11:34672025-34672075	SK-N-MC	brain:	n/a
13	chr11:34642463-34642513	H1-hESC	embryonic stem cell:	embryo
14	chr11:34675402-34675452	NB4	blood:	n/a
15	chr11:34641925-34641975	NHBE	bronchial:	n/a
16	chr11:34701819-34701869	ProgFib	skin:	n/a
17	chr11:34642303-34642353	PFSK-1	brain:	n/a
18	chr11:34642303-34642353	NB4	blood:	n/a
19	chr11:34676683-34676733	AG09319	gingival:	n/a
20	chr11:34641925-34641975	RPTEC	kidney:	n/a
21	chr11:34672025-34672075	SKMC	muscle:	n/a
22	chr11:34771918-34771968	GM12878	blood:	n/a
23	chr11:34672025-34672075	HCM	heart:	n/a
24	chr11:34675402-34675452	HRE	kidney:	n/a
25	chr11:34641925-34641975	PrEC	prostate:	n/a
26	chr11:34676683-34676733	Caco-2	colon:	n/a
27	chr11:34642885-34642935	NH-A	brain:	n/a
28	chr11:34702946-34702996	Hela-S3	cervix:	n/a
29	chr11:34681375-34681425	NHBE	bronchial:	n/a
30	chr11:34672025-34672075	MCF10A-Er-Src	breast:	n/a
31	chr11:34702946-34702996	AG09319	gingival:	n/a
32	chr11:34642303-34642353	BE2_C	brain:	n/a
33	chr11:34666060-34666110	PANC-1	pancreas:	n/a
34	chr11:34642303-34642353	HRE	kidney:	n/a
35	chr11:34672025-34672075	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:34771918-34771968	ProgFib	skin:	n/a
37	chr11:34702946-34702996	IMR90	lung:	fetal
38	chr11:34771918-34771968	GM06990	blood:	n/a
39	chr11:34771918-34771968	U87	brain:	n/a
40	chr11:34641925-34641975	NH-A	brain:	n/a
41	chr11:34642885-34642935	NHBE	bronchial:	n/a
42	chr11:34676683-34676733	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:34676683-34676733	PANC-1	pancreas:	n/a
44	chr11:34654233-34654283	HMEC	breast:	n/a
45	chr11:34642885-34642935	GM12892	blood:	n/a
46	chr11:34672025-34672075	PANC-1	pancreas:	n/a
47	chr11:34642303-34642353	RPTEC	kidney:	n/a
48	chr11:34642885-34642935	HMEC	breast:	n/a
49	chr11:34654233-34654283	ProgFib	skin:	n/a
50	chr11:34642303-34642353	HUVEC	blood vessel:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:34775760..34778139-chr11:34861633..34864027,2	K562	blood:
2	chr11:34645328..34647073-chr11:34651781..34653542,2	K562	blood:
3	chr11:34660689..34662189-chr11:34672411..34674964,2	MCF-7	breast:
4	chr11:34673700..34675383-chr11:34678871..34681043,2	K562	blood:
5	chr11:34686232..34690169-chr11:34690691..34694222,3	K562	blood:
6	chr11:34641972..34644254-chr11:34644762..34647514,2	MCF-7	breast:
7	chr11:34673816..34675543-chr11:34675726..34677757,2	K562	blood:
8	chr11:34675778..34678396-chr11:34681432..34685655,3	K562	blood:
9	chr11:34737373..34739523-chr11:34745601..34747414,2	K562	blood:
10	chr11:34660689..34662189-chr11:34672411..34674964,2	MCF-7	breast:
11	chr11:34640457..34642067-chr11:34645201..34647926,2	K562	blood:
12	chr11:34635183..34637039-chr11:34658826..34661301,2	MCF-7	breast:
13	chr11:34652609..34656733-chr11:34661493..34664204,6	MCF-7	breast:
14	chr11:34675778..34678396-chr11:34681432..34685655,3	K562	blood:
15	chr11:34670807..34672858-chr11:34677571..34680304,2	K562	blood:
16	chr11:34661817..34664108-chr11:34666612..34669231,3	MCF-7	breast:
17	chr11:34640806..34644782-chr11:34660554..34663507,4	MCF-7	breast:
18	chr11:34568608..34571143-chr11:34742934..34745851,2	K562	blood:
19	chr11:34777504..34779332-chr11:34816777..34819047,2	MCF-7	breast:
20	chr11:34608499..34609105-chr11:34675652..34676481,2	MCF-7	breast:
21	chr11:34687615..34690287-chr11:34693156..34695409,2	MCF-7	breast:
22	chr11:34736912..34738637-chr11:34937479..34939117,2	MCF-7	breast:
23	chr11:34675426..34678725-chr11:34681137..34686486,6	MCF-7	breast:
24	chr11:34671248..34673590-chr11:34674140..34675712,2	MCF-7	breast:
25	chr11:34679939..34683842-chr11:34684452..34687073,3	MCF-7	breast:
26	chr11:34679249..34681279-chr11:34681584..34684087,2	K562	blood:
27	chr11:34647092..34649318-chr11:34661381..34664170,2	MCF-7	breast:
28	chr11:34569575..34572188-chr11:34654026..34656831,2	MCF-7	breast:
29	chr11:34676055..34678665-chr11:34685926..34687942,2	MCF-7	breast:
30	chr11:34658574..34661382-chr11:34673276..34674986,2	K562	blood:
31	chr11:34741790..34743892-chr11:34746421..34748174,2	K562	blood:
32	chr11:34625607..34627154-chr11:34665407..34666959,2	MCF-7	breast:
33	chr11:34667026..34669860-chr11:34670729..34674074,4	MCF-7	breast:
34	chr11:34698695..34700932-chr11:34704220..34706433,3	K562	blood:
35	chr11:34671534..34674106-chr11:34677263..34680105,2	K562	blood:
36	chr11:34643086..34644601-chr11:34653927..34655826,2	K562	blood:
37	chr11:34643086..34644601-chr11:34653927..34655826,2	K562	blood:
38	chr11:34623810..34626247-chr11:34658951..34660726,2	K562	blood:
39	chr11:34642302..34644592-chr11:34647851..34649607,2	K562	blood:
40	chr11:34666390..34669350-chr11:34705464..34707840,2	K562	blood:
41	chr11:34660366..34662512-chr11:34808028..34810446,2	MCF-7	breast:
42	chr11:34631321..34633307-chr11:34669575..34672100,2	K562	blood:
43	chr11:34686698..34687242-chr11:34844773..34845279,2	MCF-7	breast:
44	chr11:34624693..34626791-chr11:34672431..34674013,2	K562	blood:
45	chr11:34679021..34681559-chr11:34682485..34684482,3	K562	blood:
46	chr11:34645573..34647366-chr11:34652042..34653637,2	K562	blood:
47	chr11:34652609..34656733-chr11:34661493..34664204,6	MCF-7	breast:
48	chr11:34621214..34622751-chr11:34769844..34772782,2	MCF-7	breast:
49	chr11:34685399..34688268-chr11:34690502..34692704,2	MCF-7	breast:
50	chr11:34637828..34640376-chr11:34674188..34675830,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EHF-5	chr11:34764453-34764746	NONHSAT018763
2	lnc-ELF5-3	chr11:34736881-34736897	NONHSAT018762
3	lnc-ELF5-3	chr11:34736818-34736842	NONHSAT018762
4	lnc-ELF5-3	chr11:34736903-34737435	NONHSAT018762
5	lnc-ELF5-3	chr11:34736767-34736787	NONHSAT018762
6	lnc-EHF-4	chr11:34731147-34731708	NONHSAT018761

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EHF	hsa-miR-335-5p	chr11:34681304-34681326
2	EHF	hsa-miR-335-5p	chr11:34680781-34680805

Variant related genes	Relation type
ENSG00000270491	TF binding region
EHF	TF binding region
ENSG00000271369	TF binding region
ENSG00000270491	CpG island
EHF	CpG island
ENSG00000271369	CpG island
ENSG00000135373	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000149089	chromatin interactions

Extended variants
information (count: 5018 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:5018 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs286927	chr11:34641598-34641599	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146177020	chr11:34641630-34641631	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7934718	chr11:34641650-34641651	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs188488726	chr11:34641654-34641655	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181302985	chr11:34641662-34641663	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370211849	chr11:34641666-34641667	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536979294	chr11:34641729-34641730	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs374732238	chr11:34641774-34641775	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs74905958	chr11:34641803-34641804	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185910280	chr11:34641864-34641865	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs566798635	chr11:34641912-34641913	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs139130816	chr11:34641968-34641969	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536893664	chr11:34642001-34642002	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs557107096	chr11:34642027-34642028	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577094063	chr11:34642036-34642037	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191205924	chr11:34642066-34642067	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs118050004	chr11:34642127-34642128	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541379830	chr11:34642142-34642143	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11032787	chr11:34642161-34642162	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs144035971	chr11:34642173-34642174	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs150969403	chr11:34642194-34642195	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs11032788	chr11:34642207-34642208	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs74739764	chr11:34642214-34642215	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs370217190	chr11:34642240-34642241	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs181999232	chr11:34642258-34642259	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564679616	chr11:34642284-34642285	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534209122	chr11:34642343-34642344	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs139515983	chr11:34642350-34642351	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558749760	chr11:34642365-34642366	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs547331600	chr11:34642387-34642388	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs149708466	chr11:34642440-34642441	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs286926	chr11:34642493-34642494	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs34383731	chr11:34642521-34642522	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549354083	chr11:34642551-34642552	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs34340775	chr11:34642552-34642553	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs187598028	chr11:34642620-34642621	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569291633	chr11:34642667-34642668	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs286925	chr11:34642668-34642669	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs555977215	chr11:34642672-34642673	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs286924	chr11:34642728-34642729	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs369146883	chr11:34642752-34642753	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs372910783	chr11:34642766-34642767	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs717582	chr11:34642823-34642824	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs539209994	chr11:34642865-34642866	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs552852733	chr11:34642870-34642871	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572797906	chr11:34642885-34642886	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs190965801	chr11:34642926-34642927	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs370779781	chr11:34642927-34642928	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs372370531	chr11:34642954-34642955	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs569663269	chr11:34642962-34642963	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1909 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34608400-34643600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:34625400-34642800	Weak transcription	Gastric	stomach
3	chr11:34634000-34643200	Weak transcription	Lung	lung
4	chr11:34635000-34643400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr11:34635200-34642000	Weak transcription	Esophagus	oesophagus
6	chr11:34636200-34644000	Enhancers	K562	blood
7	chr11:34636400-34641800	Weak transcription	Fetal Intestine Large	intestine
8	chr11:34637200-34641600	Weak transcription	Primary B cells from peripheral blood	blood
9	chr11:34637800-34642000	Enhancers	Stomach Mucosa	stomach
10	chr11:34637800-34649200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr11:34639000-34641600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr11:34639800-34653800	Weak transcription	Right Atrium	heart
13	chr11:34640000-34643200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:34640400-34641800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr11:34640400-34642000	Enhancers	Pancreas	Pancrea
16	chr11:34640400-34643200	Enhancers	Placenta	Placenta
17	chr11:34640800-34641800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:34641000-34641600	Enhancers	Duodenum Mucosa	Duodenum
19	chr11:34641000-34642000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr11:34641000-34642800	Enhancers	Fetal Intestine Small	intestine
21	chr11:34641000-34643400	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr11:34641200-34642400	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr11:34641400-34641800	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr11:34641400-34642000	Enhancers	NHEK	skin
25	chr11:34641400-34642200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
26	chr11:34641600-34642000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:34641600-34642200	Enhancers	Primary B cells from peripheral blood	blood
28	chr11:34641600-34642400	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr11:34641600-34642600	Enhancers	HMEC	breast
30	chr11:34641800-34642000	Enhancers	Colonic Mucosa	Colon
31	chr11:34641800-34642000	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr11:34641800-34642000	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr11:34641800-34642400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr11:34641800-34642800	Enhancers	Fetal Intestine Large	intestine
35	chr11:34641800-34644400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:34642000-34642200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr11:34642000-34642200	Flanking Active TSS	Pancreas	Pancrea
38	chr11:34642000-34642200	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr11:34642000-34642200	Enhancers	Small Intestine	intestine
40	chr11:34642000-34642200	Flanking Active TSS	Stomach Mucosa	stomach
41	chr11:34642000-34642400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:34642000-34642400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:34642000-34642400	Flanking Active TSS	Colonic Mucosa	Colon
44	chr11:34642000-34642400	Flanking Active TSS	NHEK	skin
45	chr11:34642000-34646800	Active TSS	Esophagus	oesophagus
46	chr11:34642000-34647200	Active TSS	Rectal Smooth Muscle	rectum
47	chr11:34642200-34642400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:34642200-34642400	Enhancers	Stomach Mucosa	stomach
49	chr11:34642200-34642800	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:34642200-34643200	Active TSS	Pancreatic Islets	Pancreatic Islet

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