Variant report

Variant	nsv1012946
Chromosome Location	chr2:33294522-33370391
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1039)
CpG islands
(count:734)
Chromatin interactive
region (count:87)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:33343824-33343996	K562	blood:	n/a	n/a
2	ARID3A	chr2:33366668-33366820	K562	blood:	n/a	n/a
3	ARID3A	chr2:33333652-33334321	K562	blood:	n/a	n/a
4	ARID3A	chr2:33359413-33359619	HepG2	liver:	n/a	n/a
5	ATF1	chr2:33296225-33296352	K562	blood:	n/a	n/a
6	ATF1	chr2:33333227-33334393	K562	blood:	n/a	n/a
7	ATF1	chr2:33347733-33348203	K562	blood:	n/a	n/a
8	ATF1	chr2:33294897-33295215	K562	blood:	n/a	n/a
9	ATF3	chr2:33294806-33295714	A549	lung:	n/a	n/a
10	ATF3	chr2:33294808-33295592	A549	lung:	n/a	n/a
11	ATF3	chr2:33333639-33334249	K562	blood:	n/a	n/a
12	BACH1	chr2:33333738-33333858	K562	blood:	n/a	n/a
13	BACH1	chr2:33329593-33330080	H1-hESC	embryonic stem cell:	n/a	chr2:33329934-33329948
14	BACH1	chr2:33329783-33330049	K562	blood:	n/a	chr2:33329934-33329948
15	BATF	chr2:33294981-33295180	GM12878	blood:	n/a	n/a
16	BCL3	chr2:33294764-33295617	A549	lung:	n/a	n/a
17	BCL3	chr2:33294735-33295709	A549	lung:	n/a	n/a
18	BHLHE40	chr2:33358791-33358805	K562	blood:	n/a	n/a
19	BHLHE40	chr2:33336056-33336315	HepG2	liver:	n/a	n/a
20	BHLHE40	chr2:33333586-33334367	K562	blood:	n/a	n/a
21	BHLHE40	chr2:33314483-33314612	K562	blood:	n/a	n/a
22	BRCA1	chr2:33315537-33315669	GM12878	blood:	n/a	n/a
23	BRCA1	chr2:33318891-33319051	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr2:33347614-33348187	K562	blood:	n/a	n/a
25	CBX3	chr2:33294862-33295318	K562	blood:	n/a	chr2:33294994-33295005
26	CBX3	chr2:33329649-33330320	HCT-116	colon:	n/a	n/a
27	CBX3	chr2:33333745-33334066	K562	blood:	n/a	n/a
28	CBX3	chr2:33366535-33366906	K562	blood:	n/a	n/a
29	CBX3	chr2:33333483-33334470	K562	blood:	n/a	n/a
30	CCNT2	chr2:33333652-33334227	K562	blood:	n/a	chr2:33333880-33333900
31	CCNT2	chr2:33347794-33348047	K562	blood:	n/a	n/a
32	CEBPB	chr2:33335941-33336320	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:33354474-33354674	Hela-S3	cervix:	n/a	chr2:33354581-33354592 chr2:33354594-33354605 chr2:33354583-33354594 chr2:33354593-33354606
34	CEBPB	chr2:33348419-33348450	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:33332590-33332895	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:33296545-33296867	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:33358417-33358780	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:33333731-33334076	K562	blood:	n/a	n/a
39	CEBPB	chr2:33296659-33296768	K562	blood:	n/a	n/a
40	CEBPB	chr2:33294615-33295809	HCT-116	colon:	n/a	chr2:33294846-33294859
41	CEBPB	chr2:33319378-33319669	A549	lung:	n/a	n/a
42	CEBPB	chr2:33296558-33296840	A549	lung:	n/a	n/a
43	CEBPB	chr2:33336012-33336284	MCF-7	breast:	n/a	n/a
44	CEBPB	chr2:33358491-33358702	K562	blood:	n/a	n/a
45	CEBPB	chr2:33354447-33354752	HepG2	liver:	n/a	chr2:33354581-33354592 chr2:33354594-33354605 chr2:33354583-33354594 chr2:33354593-33354606
46	CEBPB	chr2:33294925-33295611	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr2:33333772-33334163	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:33294853-33295631	A549	lung:	n/a	n/a
49	CEBPB	chr2:33354448-33354711	IMR90	lung:	n/a	chr2:33354581-33354592 chr2:33354594-33354605 chr2:33354583-33354594 chr2:33354593-33354606
50	CEBPB	chr2:33333587-33334261	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:33368461-33368511	NH-A	brain:	n/a
2	chr2:33359356-33359406	HCT-116	colon:	n/a
3	chr2:33368461-33368511	NH-A	brain:	n/a
4	chr2:33359356-33359406	HCT-116	colon:	n/a
5	chr2:33368461-33368511	HUVEC	blood vessel:	n/a
6	chr2:33359356-33359406	BE2_C	brain:	n/a
7	chr2:33342294-33342344	GM12891	blood:	n/a
8	chr2:33317174-33317224	HepG2	liver:	n/a
9	chr2:33359356-33359406	HCF	heart:	n/a
10	chr2:33359550-33359600	T-47D	breast:	n/a
11	chr2:33368461-33368511	BJ	skin:	n/a
12	chr2:33359529-33359579	HUVEC	blood vessel:	n/a
13	chr2:33359198-33359248	AoSMC	blood vessel:	n/a
14	chr2:33359688-33359738	PANC-1	pancreas:	n/a
15	chr2:33359356-33359406	ovcar-3	ovarian:	n/a
16	chr2:33359550-33359600	HUVEC	blood vessel:	n/a
17	chr2:33311428-33311478	K562	blood:	n/a
18	chr2:33311428-33311478	SK-N-SH	brain:	n/a
19	chr2:33359198-33359248	HL-60	blood:	n/a
20	chr2:33359356-33359406	LNCaP	prostate:	n/a
21	chr2:33317174-33317224	RPTEC	kidney:	n/a
22	chr2:33368461-33368511	ovcar-3	ovarian:	n/a
23	chr2:33359550-33359600	K562	blood:	n/a
24	chr2:33348262-33348312	CMK	blood:	n/a
25	chr2:33359198-33359248	NB4	blood:	n/a
26	chr2:33295138-33295188	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:33359281-33359331	HRCEpiC	kidney:	n/a
28	chr2:33359688-33359738	MCF-7	breast:	n/a
29	chr2:33317174-33317224	GM12891	blood:	n/a
30	chr2:33359356-33359406	NHBE	bronchial:	n/a
31	chr2:33359198-33359248	K562	blood:	n/a
32	chr2:33359550-33359600	HAEpiC	amniotic membrane:	n/a
33	chr2:33348262-33348312	HEEpiC	esophagus:	n/a
34	chr2:33359281-33359331	A549	lung:	n/a
35	chr2:33295138-33295188	H1-hESC	embryonic stem cell:	embryo
36	chr2:33368461-33368511	GM12891	blood:	n/a
37	chr2:33368461-33368511	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:33295138-33295188	AG04449	skin:	fetal
39	chr2:33368461-33368511	ECC-1	luminal epithelium:	n/a
40	chr2:33348262-33348312	K562	blood:	n/a
41	chr2:33359550-33359600	HRPEpiC	eye:	n/a
42	chr2:33359529-33359579	T-47D	breast:	n/a
43	chr2:33295138-33295188	HRPEpiC	eye:	n/a
44	chr2:33359198-33359248	HNPCEpiC	eye:	n/a
45	chr2:33359529-33359579	GM06990	blood:	n/a
46	chr2:33359281-33359331	MCF-7	breast:	n/a
47	chr2:33317174-33317224	ECC-1	luminal epithelium:	n/a
48	chr2:33368461-33368511	K562	blood:	n/a
49	chr2:33311428-33311478	ECC-1	luminal epithelium:	n/a
50	chr2:33359688-33359738	AG04449	skin:	fetal

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:33333082..33335535-chr2:33335888..33338274,2	K562	blood:
2	chr2:33287772..33292165-chr2:33292341..33295822,9	MCF-7	breast:
3	chr2:33360698..33363585-chr2:33365349..33368333,2	K562	blood:
4	chr2:33292854..33294446-chr2:33300367..33303363,2	K562	blood:
5	chr2:33333082..33335535-chr2:33335888..33338274,2	K562	blood:
6	chr2:33293451..33296755-chr2:33301954..33305143,4	MCF-7	breast:
7	chr2:33294946..33295843-chr8:91562977..91563667,2	MCF-7	breast:
8	chr2:33294989..33295888-chr2:33416957..33417785,6	MCF-7	breast:
9	chr2:33295214..33297626-chr2:33299821..33301525,2	K562	blood:
10	chr2:32997868..32998558-chr2:33311540..33312044,2	K562	blood:
11	chr2:33297892..33300228-chr2:33302615..33306075,3	MCF-7	breast:
12	chr2:33363634..33367831-chr2:33371387..33375003,3	K562	blood:
13	chr2:33325612..33327794-chr2:33340279..33342950,2	MCF-7	breast:
14	chr2:33295981..33298155-chr2:33304588..33306275,2	K562	blood:
15	chr2:33323744..33329444-chr2:33330202..33334725,9	K562	blood:
16	chr2:33170888..33171729-chr2:33294522..33295845,3	MCF-7	breast:
17	chr2:33347601..33349574-chr2:33351512..33354132,2	K562	blood:
18	chr2:33315357..33320010-chr2:33321376..33324681,5	K562	blood:
19	chr2:33172001..33174458-chr2:33303500..33306499,2	MCF-7	breast:
20	chr2:33295981..33298155-chr2:33304588..33306275,2	K562	blood:
21	chr2:33319782..33321597-chr2:33324862..33327252,2	K562	blood:
22	chr2:33355814..33359074-chr2:33359730..33364790,5	K562	blood:
23	chr2:33294529..33295807-chr2:33416903..33417827,9	MCF-7	breast:
24	chr2:33294991..33295910-chr2:33416929..33417799,3	MCF-7	breast:
25	chr2:33295214..33297626-chr2:33299821..33301525,2	K562	blood:
26	chr2:33284687..33288170-chr2:33293184..33297507,4	K562	blood:
27	chr2:33321965..33324050-chr2:33326516..33328893,2	K562	blood:
28	chr2:33341850..33346633-chr2:33347912..33351586,5	K562	blood:
29	chr2:33359671..33361313-chr2:33368452..33370513,2	K562	blood:
30	chr2:33332965..33336318-chr2:33345461..33348526,4	K562	blood:
31	chr2:33325612..33327794-chr2:33340279..33342950,2	MCF-7	breast:
32	chr2:33294968..33295923-chr2:33594558..33595514,5	MCF-7	breast:
33	chr2:33320811..33323465-chr2:33327393..33329847,2	K562	blood:
34	chr2:33350370..33352702-chr2:33358225..33360528,2	K562	blood:
35	chr2:33294964..33297126-chr2:33297596..33299242,2	MCF-7	breast:
36	chr2:33321965..33324050-chr2:33326516..33328893,2	K562	blood:
37	chr2:33325545..33328306-chr2:33331227..33333844,3	K562	blood:
38	chr2:33323744..33329444-chr2:33330202..33334725,9	K562	blood:
39	chr2:33346676..33349370-chr2:33351753..33353323,2	MCF-7	breast:
40	chr2:33294735..33295813-chr2:33311218..33312090,5	MCF-7	breast:
41	chr2:33347601..33349574-chr2:33351512..33354132,2	K562	blood:
42	chr2:33360698..33363585-chr2:33365349..33368333,2	K562	blood:
43	chr2:33342989..33344574-chr2:33349726..33351939,2	K562	blood:
44	chr2:33341850..33346633-chr2:33347912..33351586,5	K562	blood:
45	chr2:33360506..33363015-chr2:33369952..33372450,2	K562	blood:
46	chr2:33368241..33370517-chr2:33370553..33373234,2	K562	blood:
47	chr2:33294930..33295688-chr2:33444908..33445678,2	MCF-7	breast:
48	chr1:22780784..22781462-chr2:33294993..33295833,2	MCF-7	breast:
49	chr2:33352861..33355600-chr2:33385791..33387865,2	MCF-7	breast:
50	chr2:33357374..33360115-chr2:33361788..33364595,2	K562	blood:

No data

Variant related genes	Relation type
LTBP1	TF binding region
LTBP1	CpG island
ENSG00000049323	chromatin interactions
ENSG00000223951	chromatin interactions
ENSG00000206951	chromatin interactions

Extended variants
information (count: 3305 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3305 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559449397	chr2:33294524-33294525	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs558661725	chr2:33294530-33294531	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs572146035	chr2:33294531-33294532	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs35193442	chr2:33294629-33294630	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs147871039	chr2:33294633-33294634	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs141696403	chr2:33294660-33294661	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs574753787	chr2:33294696-33294697	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs372753456	chr2:33294729-33294730	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs79033019	chr2:33294731-33294732	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs543764665	chr2:33294749-33294750	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs562694863	chr2:33294750-33294751	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs150427075	chr2:33294757-33294758	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs145358739	chr2:33294773-33294774	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs186750628	chr2:33294775-33294776	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs149180150	chr2:33294801-33294802	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs191888576	chr2:33294828-33294829	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs567534904	chr2:33294837-33294838	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs536518820	chr2:33294899-33294900	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs184078853	chr2:33294923-33294924	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs115068480	chr2:33294930-33294931	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs538675609	chr2:33294934-33294935	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs558349019	chr2:33294939-33294940	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs143400229	chr2:33294946-33294947	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs534727054	chr2:33295040-33295041	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs34111447	chr2:33295048-33295049	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs116663415	chr2:33295082-33295083	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs574689570	chr2:33295087-33295088	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs543702067	chr2:33295129-33295130	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs148368706	chr2:33295139-33295140	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs576354222	chr2:33295149-33295150	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs545411061	chr2:33295160-33295161	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs142232576	chr2:33295180-33295181	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs564564155	chr2:33295261-33295262	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs527745022	chr2:33295269-33295270	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs145290206	chr2:33295302-33295303	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs530131266	chr2:33295343-33295344	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs17324986	chr2:33295402-33295403	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs190323132	chr2:33295404-33295405	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs374231667	chr2:33295434-33295435	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs181522124	chr2:33295435-33295436	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs547205734	chr2:33295484-33295485	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs145906077	chr2:33295491-33295492	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs570356767	chr2:33295544-33295545	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs531996568	chr2:33295556-33295557	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs185700147	chr2:33295576-33295577	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs563713962	chr2:33295588-33295589	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs565703921	chr2:33295603-33295604	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs565709036	chr2:33295607-33295608	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs439416	chr2:33295631-33295632	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs142461357	chr2:33295674-33295675	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1392 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33260200-33295400	Weak transcription	Right Atrium	heart
2	chr2:33289600-33308200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:33292000-33298200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr2:33292000-33299200	Enhancers	HUVEC	blood vessel
5	chr2:33292200-33295200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:33292200-33296800	Enhancers	NHDF-Ad	bronchial
7	chr2:33292400-33295200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:33292400-33295200	Enhancers	NHEK	skin
9	chr2:33292400-33296800	Enhancers	NHLF	lung
10	chr2:33292600-33294800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr2:33292800-33294600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr2:33292800-33294600	Enhancers	HMEC	breast
13	chr2:33292800-33295200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:33292800-33295400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr2:33292800-33296200	Enhancers	HSMM	muscle
16	chr2:33292800-33296200	Enhancers	NH-A	brain
17	chr2:33292800-33297000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:33293200-33294600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:33293200-33294800	Enhancers	Osteobl	bone
20	chr2:33293400-33295600	Enhancers	Rectal Smooth Muscle	rectum
21	chr2:33293400-33295800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr2:33293600-33294800	Weak transcription	Colon Smooth Muscle	Colon
23	chr2:33293800-33294800	Weak transcription	Fetal Lung	lung
24	chr2:33294000-33295200	Enhancers	Stomach Smooth Muscle	stomach
25	chr2:33294000-33295600	Enhancers	K562	blood
26	chr2:33294000-33295800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr2:33294000-33297400	Enhancers	Placenta Amnion	Placenta Amnion
28	chr2:33294000-33297800	Enhancers	Right Ventricle	heart
29	chr2:33294200-33295000	Enhancers	Lung	lung
30	chr2:33294200-33296000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:33294200-33296000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr2:33294200-33296000	Enhancers	Aorta	Aorta
33	chr2:33294200-33296000	Enhancers	Ovary	ovary
34	chr2:33294200-33296400	Enhancers	Esophagus	oesophagus
35	chr2:33294200-33297000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:33294200-33297200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:33294200-33297600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr2:33294200-33297600	Enhancers	Left Ventricle	heart
39	chr2:33294200-33299600	Enhancers	Placenta	Placenta
40	chr2:33294400-33294600	Enhancers	Liver	Liver
41	chr2:33294400-33295000	Enhancers	Psoas Muscle	Psoas
42	chr2:33294400-33295000	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr2:33294400-33295200	Enhancers	HSMMtube	muscle
44	chr2:33294400-33295400	Weak transcription	Fetal Stomach	stomach
45	chr2:33294400-33295400	Enhancers	Hela-S3	cervix
46	chr2:33294400-33295600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr2:33294400-33295800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr2:33294400-33296000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr2:33294400-33296000	Enhancers	Pancreas	Pancrea
50	chr2:33294400-33296200	Enhancers	Stomach Mucosa	stomach

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