Variant report

Variant	nsv546818
Chromosome Location	chr1:92236048-92579206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4357)
CpG islands
(count:4521)
Chromatin interactive
region (count:115)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4357 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:92283136-92283452	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:92545681-92545684	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:92504254-92504757	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:92392911-92393150	K562	blood:	n/a	n/a
5	ARID3A	chr1:92317145-92317468	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:92463047-92463494	K562	blood:	n/a	n/a
7	ARID3A	chr1:92348918-92349315	K562	blood:	n/a	n/a
8	ARID3A	chr1:92348921-92349309	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:92258609-92258748	K562	blood:	n/a	n/a
10	ARID3A	chr1:92310527-92311162	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:92282827-92282923	K562	blood:	n/a	n/a
12	ARID3A	chr1:92295888-92296212	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:92292432-92293961	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:92272469-92272669	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:92351242-92351293	HepG2	liver:	n/a	n/a
16	ARID3A	chr1:92256925-92256931	K562	blood:	n/a	n/a
17	ARID3A	chr1:92424619-92424819	HepG2	liver:	n/a	n/a
18	ARID3A	chr1:92463265-92463529	HepG2	liver:	n/a	n/a
19	ARID3A	chr1:92392821-92393186	HepG2	liver:	n/a	n/a
20	ARID3A	chr1:92300668-92300994	HepG2	liver:	n/a	n/a
21	ARID3A	chr1:92281548-92281943	HepG2	liver:	n/a	n/a
22	ARID3A	chr1:92296732-92297514	HepG2	liver:	n/a	chr1:92297485-92297501
23	ARID3A	chr1:92545717-92545724	K562	blood:	n/a	n/a
24	ARID3A	chr1:92344000-92344448	HepG2	liver:	n/a	n/a
25	ARID3A	chr1:92351519-92352531	HepG2	liver:	n/a	n/a
26	ARID3A	chr1:92285078-92285270	HepG2	liver:	n/a	n/a
27	ATF1	chr1:92530637-92530857	K562	blood:	n/a	n/a
28	ATF1	chr1:92270129-92270816	K562	blood:	n/a	n/a
29	ATF1	chr1:92360017-92360202	K562	blood:	n/a	n/a
30	ATF2	chr1:92269217-92270649	GM12878	blood:	n/a	n/a
31	ATF2	chr1:92343239-92343765	GM12878	blood:	n/a	n/a
32	ATF2	chr1:92343078-92343855	GM12878	blood:	n/a	n/a
33	ATF2	chr1:92269352-92269901	GM12878	blood:	n/a	n/a
34	ATF2	chr1:92341664-92342230	GM12878	blood:	n/a	n/a
35	ATF2	chr1:92270002-92270575	GM12878	blood:	n/a	n/a
36	ATF2	chr1:92338008-92338650	GM12878	blood:	n/a	n/a
37	ATF2	chr1:92338095-92338511	GM12878	blood:	n/a	n/a
38	ATF3	chr1:92270157-92270708	K562	blood:	n/a	n/a
39	ATF3	chr1:92414808-92414936	K562	blood:	n/a	chr1:92414878-92414887 chr1:92414867-92414887
40	ATF3	chr1:92351477-92351827	A549	lung:	n/a	n/a
41	BACH1	chr1:92494875-92495995	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr1:92283656-92284243	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr1:92290748-92290750	K562	blood:	n/a	n/a
44	BACH1	chr1:92331752-92331754	K562	blood:	n/a	n/a
45	BACH1	chr1:92352167-92352293	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr1:92458760-92458932	K562	blood:	n/a	n/a
47	BACH1	chr1:92351076-92351915	H1-hESC	embryonic stem cell:	n/a	n/a
48	BATF	chr1:92343331-92343754	GM12878	blood:	n/a	chr1:92343581-92343591 chr1:92343580-92343591
49	BATF	chr1:92270038-92270570	GM12878	blood:	n/a	chr1:92270274-92270285 chr1:92270275-92270285
50	BATF	chr1:92269440-92269754	GM12878	blood:	n/a	n/a

(count:4521 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92546135-92546185	GM12892	blood:	n/a
2	chr1:92414221-92414271	HRE	kidney:	n/a
3	chr1:92350786-92350836	SK-N-SH_RA	brain:	n/a
4	chr1:92494997-92495047	GM19239	blood:	n/a
5	chr1:92545888-92545938	HMEC	breast:	n/a
6	chr1:92284280-92284330	NH-A	brain:	n/a
7	chr1:92347850-92347900	T-47D	breast:	n/a
8	chr1:92546135-92546185	GM12892	blood:	n/a
9	chr1:92414221-92414271	HRE	kidney:	n/a
10	chr1:92350786-92350836	SK-N-SH_RA	brain:	n/a
11	chr1:92494997-92495047	GM19239	blood:	n/a
12	chr1:92545888-92545938	HMEC	breast:	n/a
13	chr1:92284280-92284330	NH-A	brain:	n/a
14	chr1:92347850-92347900	T-47D	breast:	n/a
15	chr1:92351487-92351537	NH-A	brain:	n/a
16	chr1:92546470-92546520	HL-60	blood:	n/a
17	chr1:92284280-92284330	GM19239	blood:	n/a
18	chr1:92414344-92414394	HRE	kidney:	n/a
19	chr1:92350112-92350162	NH-A	brain:	n/a
20	chr1:92350133-92350183	CMK	blood:	n/a
21	chr1:92347850-92347900	AG09309	skin:	n/a
22	chr1:92413007-92413057	Jurkat	blood:	n/a
23	chr1:92270513-92270563	U87	brain:	n/a
24	chr1:92542467-92542517	HNPCEpiC	eye:	n/a
25	chr1:92495004-92495054	A549	lung:	n/a
26	chr1:92542467-92542517	GM12878	blood:	n/a
27	chr1:92352407-92352457	SK-N-SH_RA	brain:	n/a
28	chr1:92494898-92494948	ovcar-3	ovarian:	n/a
29	chr1:92549234-92549284	HL-60	blood:	n/a
30	chr1:92413007-92413057	LNCaP	prostate:	n/a
31	chr1:92545580-92545630	ovcar-3	ovarian:	n/a
32	chr1:92546479-92546529	GM12878	blood:	n/a
33	chr1:92351695-92351745	AG09309	skin:	n/a
34	chr1:92352084-92352134	HEEpiC	esophagus:	n/a
35	chr1:92545580-92545630	Hepatocyte	liver:	n/a
36	chr1:92545768-92545818	NT2-D1	testis:	n/a
37	chr1:92351547-92351597	Hela-S3	cervix:	n/a
38	chr1:92545662-92545712	ProgFib	skin:	n/a
39	chr1:92263858-92263908	AG04450	lung:	fetal
40	chr1:92545650-92545700	HRPEpiC	eye:	n/a
41	chr1:92546040-92546090	PFSK-1	brain:	n/a
42	chr1:92414344-92414394	ovcar-3	ovarian:	n/a
43	chr1:92545224-92545274	NHBE	bronchial:	n/a
44	chr1:92338262-92338312	NHDF-neo	bronchial:	n/a
45	chr1:92355253-92355303	GM06990	blood:	n/a
46	chr1:92350430-92350480	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:92282206-92282256	NHDF-neo	bronchial:	n/a
48	chr1:92545888-92545938	AG10803	skin:	n/a
49	chr1:92545662-92545712	U87	brain:	n/a
50	chr1:92495818-92495868	PFSK-1	brain:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:92309780..92313855-chr1:92314421..92317529,4	K562	blood:
2	chr1:92269279..92272009-chr1:92273334..92276001,3	K562	blood:
3	chr1:92245858..92248144-chr1:92269665..92271280,2	K562	blood:
4	chr1:92329344..92331517-chr1:92335405..92337042,2	K562	blood:
5	chr1:92202754..92203402-chr1:92392489..92393086,2	MCF-7	breast:
6	chr1:92271912..92274176-chr1:92284969..92287951,2	K562	blood:
7	chr1:92287190..92288888-chr1:92292910..92295655,2	K562	blood:
8	chr1:92519730..92522449-chr1:92522597..92525189,3	K562	blood:
9	chr1:92242856..92244541-chr1:92248702..92251001,2	K562	blood:
10	chr1:92316915..92318823-chr1:92321459..92323103,2	K562	blood:
11	chr1:92493964..92495908-chr1:92496400..92499100,2	K562	blood:
12	chr1:92545812..92549091-chr1:92549918..92553923,4	K562	blood:
13	chr1:92306378..92308491-chr1:92309526..92312029,2	K562	blood:
14	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
15	chr1:92359622..92362110-chr1:92365556..92367175,2	K562	blood:
16	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
17	chr1:92411395..92413821-chr1:92420439..92422796,2	K562	blood:
18	chr1:91995716..91996502-chr1:92392369..92393018,2	MCF-7	breast:
19	chr1:92249408..92251334-chr1:92252607..92255578,2	K562	blood:
20	chr1:92494787..92497358-chr1:92544717..92548251,3	MCF-7	breast:
21	chr1:92226383..92229371-chr1:92235062..92236732,2	K562	blood:
22	chr1:92531679..92534472-chr1:92536505..92538325,2	K562	blood:
23	chr1:92500741..92502488-chr1:92762793..92765174,2	MCF-7	breast:
24	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:
25	chr1:92329344..92331517-chr1:92335405..92337042,2	K562	blood:
26	chr1:92506546..92509433-chr1:92514602..92517083,2	K562	blood:
27	chr1:92306378..92308491-chr1:92309526..92312029,2	K562	blood:
28	chr1:92556197..92558083-chr1:92563000..92565811,2	MCF-7	breast:
29	chr1:92415221..92417669-chr1:92420291..92422618,2	K562	blood:
30	chr1:92249408..92251334-chr1:92252607..92255578,2	K562	blood:
31	chr1:92357381..92360848-chr1:92361441..92364289,5	K562	blood:
32	chr1:92262741..92265780-chr1:92267189..92269576,3	K562	blood:
33	chr1:92345504..92347682-chr1:92351569..92354342,2	MCF-7	breast:
34	chr1:92252697..92255267-chr1:92255906..92257431,2	K562	blood:
35	chr1:92258357..92261493-chr1:92263209..92266078,3	K562	blood:
36	chr1:92274050..92276390-chr1:92277677..92279989,2	K562	blood:
37	chr1:92341690..92345444-chr1:92349151..92352209,5	K562	blood:
38	chr1:92288953..92291560-chr1:92301020..92303109,3	K562	blood:
39	chr1:92506546..92509433-chr1:92514602..92517083,2	K562	blood:
40	chr1:92418160..92421480-chr1:92423319..92426988,3	K562	blood:
41	chr1:91976600..91979219-chr1:92351174..92353398,2	MCF-7	breast:
42	chr1:92237802..92240400-chr1:92241191..92243565,2	K562	blood:
43	chr1:91994551..91996997-chr1:92385610..92388191,2	K562	blood:
44	chr1:92529998..92532866-chr1:92545519..92547678,2	MCF-7	breast:
45	chr1:91869631..91870341-chr1:92392565..92393108,2	K562	blood:
46	chr1:92082754..92083639-chr1:92392516..92393512,4	MCF-7	breast:
47	chr1:92350409..92353610-chr1:92359343..92362400,3	K562	blood:
48	chr1:92242856..92244541-chr1:92248702..92251001,2	K562	blood:
49	chr1:92262741..92265780-chr1:92267189..92269576,3	K562	blood:
50	chr1:92535153..92538093-chr1:92546590..92548474,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HFM1-3	chr1:92351587-92351708	NONHSAT004441
2	lnc-EPHX4-2	chr1:92415457-92415856	NONHSAT004444
3	lnc-GLMN-2	chr1:92295333-92295631	NONHSAT004440
4	lnc-EPHX4-2	chr1:92415447-92415869	NONHSAT004446
5	lnc-EPHX4-2	chr1:92414955-92415045	NONHSAT004445
6	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004443
7	lnc-EPHX4-2	chr1:92414955-92415076	NONHSAT004444
8	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004444
9	lnc-BRDT-1	chr1:92404826-92405131	NONHSAT004442
10	lnc-HFM1-3	chr1:92329396-92329836	NONHSAT004441
11	lnc-EPHX4-2	chr1:92415447-92415889	NONHSAT004445
12	lnc-EPHX4-2	chr1:92414955-92415045	NONHSAT004443
13	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004445
14	lnc-EPHX4-2	chr1:92415457-92415859	NONHSAT004443
15	lnc-EPHX4-2	chr1:92415195-92415239	NONHSAT004446
16	lnc-EPHX4-2	chr1:92414960-92415076	NONHSAT004446

No data

Variant related genes	Relation type
LPCAT2BP	TF binding region
RN7SL653P	TF binding region
TGFBR3	TF binding region
BTBD8	TF binding region
SETSIP	TF binding region
BRDT	TF binding region
EPHX4	TF binding region
RN7SL235P	TF binding region
LPCAT2BP	CpG island
RN7SL653P	CpG island
TGFBR3	CpG island
BTBD8	CpG island
SETSIP	CpG island
BRDT	CpG island
EPHX4	CpG island
RN7SL235P	CpG island
ENSG00000097046	chromatin interactions
ENSG00000116830	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000189195	chromatin interactions
ENSG00000172031	chromatin interactions
ENSG00000069702	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000162669	chromatin interactions
ENSG00000239794	chromatin interactions
ENSG00000233228	chromatin interactions

Extended variants
information (count: 10280 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:10280 , 50 per page) page: 1 2 3 4 5 6 7 ... 206

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs284191	chr1:92236048-92236049	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556303416	chr1:92236050-92236051	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566204766	chr1:92236057-92236058	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs17883681	chr1:92236065-92236066	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs284192	chr1:92236078-92236079	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs560365551	chr1:92236095-92236096	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572400104	chr1:92236145-92236146	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542852138	chr1:92236197-92236198	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs17878451	chr1:92236247-92236248	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs573251831	chr1:92236265-92236266	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs531329809	chr1:92236308-92236309	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs17881382	chr1:92236310-92236311	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs35712852	chr1:92236313-92236314	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs114131625	chr1:92236329-92236330	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6700529	chr1:92236342-92236343	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186175493	chr1:92236365-92236366	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566019834	chr1:92236374-92236375	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530002365	chr1:92236382-92236383	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548434116	chr1:92236408-92236409	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544638542	chr1:92236411-92236412	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145752302	chr1:92236421-92236422	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189187193	chr1:92236430-92236431	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17881865	chr1:92236468-92236469	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs72967150	chr1:92236517-92236518	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375345048	chr1:92236613-92236614	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538692367	chr1:92236652-92236653	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113887480	chr1:92236699-92236700	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553737179	chr1:92236733-92236734	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12039411	chr1:92236761-92236762	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542889095	chr1:92236770-92236771	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554882189	chr1:92236771-92236772	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576542157	chr1:92236892-92236893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370744137	chr1:92236912-92236913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180871328	chr1:92236928-92236929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs284193	chr1:92237000-92237001	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs17884240	chr1:92237028-92237029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs284194	chr1:92237037-92237038	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs369017041	chr1:92237048-92237049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373334829	chr1:92237053-92237054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113251819	chr1:92237089-92237090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs284195	chr1:92237120-92237121	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548430491	chr1:92237155-92237156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376513421	chr1:92237195-92237196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569758510	chr1:92237218-92237219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529455848	chr1:92237233-92237234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371641852	chr1:92237263-92237264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535320917	chr1:92237276-92237277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199554837	chr1:92237283-92237284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552083319	chr1:92237318-92237319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs17879255	chr1:92237361-92237362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:5982 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92204800-92247000	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr1:92216800-92241800	Weak transcription	Aorta	Aorta
3	chr1:92217800-92247800	Weak transcription	Small Intestine	intestine
4	chr1:92219400-92238200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:92220600-92255800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:92221000-92248000	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr1:92224400-92242800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr1:92225400-92241600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:92226600-92236400	Weak transcription	Brain Substantia Nigra	brain
10	chr1:92227000-92257200	Weak transcription	Fetal Intestine Small	intestine
11	chr1:92229200-92241600	Weak transcription	Esophagus	oesophagus
12	chr1:92230200-92240800	Weak transcription	Right Atrium	heart
13	chr1:92230400-92242400	Weak transcription	Lung	lung
14	chr1:92230600-92247800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:92231000-92246800	Weak transcription	Hela-S3	cervix
16	chr1:92231200-92236400	Weak transcription	Fetal Lung	lung
17	chr1:92231200-92238200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:92231200-92240200	Weak transcription	Pancreas	Pancrea
19	chr1:92231400-92242600	Weak transcription	Stomach Mucosa	stomach
20	chr1:92232600-92243200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr1:92232800-92237400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:92233200-92257000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:92233400-92246800	Weak transcription	A549	lung
24	chr1:92234000-92236800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:92234400-92236400	Enhancers	NHLF	lung
26	chr1:92234400-92236800	Enhancers	Fetal Muscle Leg	muscle
27	chr1:92234400-92236800	Enhancers	Stomach Smooth Muscle	stomach
28	chr1:92234600-92236600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr1:92234600-92236800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:92234600-92236800	Genic enhancers	NHDF-Ad	bronchial
31	chr1:92234800-92236800	Genic enhancers	HepG2	liver
32	chr1:92235000-92236600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:92235000-92236800	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:92235000-92236800	Enhancers	Liver	Liver
35	chr1:92235200-92240800	Weak transcription	Fetal Muscle Trunk	muscle
36	chr1:92235400-92236800	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr1:92235400-92238600	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr1:92235400-92239000	Weak transcription	Ovary	ovary
39	chr1:92235400-92242400	Weak transcription	Fetal Stomach	stomach
40	chr1:92235600-92237000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr1:92235600-92237400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:92235600-92239800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr1:92235600-92239800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:92235600-92240800	Weak transcription	Placenta	Placenta
45	chr1:92235600-92241600	Weak transcription	Spleen	Spleen
46	chr1:92235600-92242200	Weak transcription	Psoas Muscle	Psoas
47	chr1:92235600-92242400	Weak transcription	Left Ventricle	heart
48	chr1:92235600-92242600	Weak transcription	Fetal Heart	heart
49	chr1:92235600-92243200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:92235600-92243600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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