Variant report

Variant	nsv536557
Chromosome Location	chr3:46706571-46853434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2001)
CpG islands
(count:4522)
Chromatin interactive
region (count:157)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2001 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:46755483-46755920	GM12878	blood:	n/a	n/a
2	ATF2	chr3:46755533-46755773	GM12878	blood:	n/a	n/a
3	ATF2	chr3:46746461-46746813	GM12878	blood:	n/a	n/a
4	ATF2	chr3:46759302-46759627	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr3:46792308-46792631	K562	blood:	n/a	n/a
6	ATF3	chr3:46759282-46759598	K562	blood:	n/a	n/a
7	ATF3	chr3:46759265-46759598	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr3:46792267-46792609	K562	blood:	n/a	n/a
9	ATF3	chr3:46759331-46759550	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:46746558-46746758	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:46759334-46759543	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:46735430-46735744	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:46734048-46734515	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr3:46720127-46720375	GM12878	blood:	n/a	n/a
15	BATF	chr3:46773261-46773680	GM12878	blood:	n/a	n/a
16	BATF	chr3:46755501-46755889	GM12878	blood:	n/a	n/a
17	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
18	BATF	chr3:46773278-46773701	GM12878	blood:	n/a	n/a
19	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
20	BATF	chr3:46755589-46755797	GM12878	blood:	n/a	n/a
21	BATF	chr3:46720130-46720422	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:46755551-46755755	GM12878	blood:	n/a	chr3:46755588-46755601
24	BCL11A	chr3:46755446-46755860	GM12878	blood:	n/a	chr3:46755588-46755601
25	BCL3	chr3:46755447-46755829	GM12878	blood:	n/a	chr3:46755588-46755601
26	BCLAF1	chr3:46759179-46759647	K562	blood:	n/a	n/a
27	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
28	BHLHE40	chr3:46773339-46773653	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:46735446-46735593	K562	blood:	n/a	n/a
30	BHLHE40	chr3:46755577-46755866	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:46736761-46737392	K562	blood:	n/a	n/a
32	BHLHE40	chr3:46746528-46746852	K562	blood:	n/a	n/a
33	BHLHE40	chr3:46759435-46759439	K562	blood:	n/a	n/a
34	BHLHE40	chr3:46734493-46734748	K562	blood:	n/a	n/a
35	BHLHE40	chr3:46734263-46734269	A549	lung:	n/a	n/a
36	BHLHE40	chr3:46736984-46737365	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
38	BRCA1	chr3:46708976-46709045	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr3:46755567-46755723	GM12878	blood:	n/a	n/a
40	BRCA1	chr3:46759337-46759615	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr3:46734876-46735076	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr3:46746485-46746854	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr3:46746586-46746696	HepG2	liver:	n/a	n/a
44	BRCA1	chr3:46746601-46746847	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
46	CBX3	chr3:46759328-46759544	K562	blood:	n/a	n/a
47	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
48	CBX3	chr3:46759289-46759662	K562	blood:	n/a	n/a
49	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
50	CCNT2	chr3:46759152-46759605	K562	blood:	n/a	n/a

(count:4522 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46759335-46759385	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:46752152-46752202	H1-hESC	embryonic stem cell:	embryo
3	chr3:46718369-46718419	AG09309	skin:	n/a
4	chr3:46718990-46719040	SK-N-SH	brain:	n/a
5	chr3:46733475-46733525	HPAEpiC	pulmonary alveolar:	n/a
6	chr3:46775544-46775594	NB4	blood:	n/a
7	chr3:46735338-46735388	GM06990	blood:	n/a
8	chr3:46789735-46789785	ovcar-3	ovarian:	n/a
9	chr3:46759335-46759385	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:46752152-46752202	H1-hESC	embryonic stem cell:	embryo
11	chr3:46718369-46718419	AG09309	skin:	n/a
12	chr3:46718990-46719040	SK-N-SH	brain:	n/a
13	chr3:46733475-46733525	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:46775544-46775594	NB4	blood:	n/a
15	chr3:46735338-46735388	GM06990	blood:	n/a
16	chr3:46789735-46789785	ovcar-3	ovarian:	n/a
17	chr3:46730941-46730991	NT2-D1	testis:	n/a
18	chr3:46759335-46759385	SK-N-MC	brain:	n/a
19	chr3:46775544-46775594	Hela-S3	cervix:	n/a
20	chr3:46735695-46735745	RPTEC	kidney:	n/a
21	chr3:46742865-46742915	ovcar-3	ovarian:	n/a
22	chr3:46799010-46799060	BE2_C	brain:	n/a
23	chr3:46785957-46786007	SK-N-SH_RA	brain:	n/a
24	chr3:46801208-46801258	GM12892	blood:	n/a
25	chr3:46746779-46746829	HAEpiC	amniotic membrane:	n/a
26	chr3:46787073-46787123	NHBE	bronchial:	n/a
27	chr3:46768322-46768372	HepG2	liver:	n/a
28	chr3:46786387-46786437	HEK293	kidney:	embryo
29	chr3:46718941-46718991	SKMC	muscle:	n/a
30	chr3:46719086-46719136	PrEC	prostate:	n/a
31	chr3:46797928-46797978	HRCEpiC	kidney:	n/a
32	chr3:46761555-46761605	HUVEC	blood vessel:	n/a
33	chr3:46787073-46787123	ProgFib	skin:	n/a
34	chr3:46730941-46730991	GM06990	blood:	n/a
35	chr3:46759472-46759522	PANC-1	pancreas:	n/a
36	chr3:46735315-46735365	U87	brain:	n/a
37	chr3:46759698-46759748	AG04450	lung:	fetal
38	chr3:46791477-46791527	BE2_C	brain:	n/a
39	chr3:46742491-46742541	NT2-D1	testis:	n/a
40	chr3:46742865-46742915	LNCaP	prostate:	n/a
41	chr3:46759096-46759146	AG04449	skin:	fetal
42	chr3:46735009-46735059	SAEC	small airway:	n/a
43	chr3:46735801-46735851	NHDF-neo	bronchial:	n/a
44	chr3:46733475-46733525	GM19239	blood:	n/a
45	chr3:46790182-46790232	GM19239	blood:	n/a
46	chr3:46719625-46719675	SKMC	muscle:	n/a
47	chr3:46789735-46789785	GM12891	blood:	n/a
48	chr3:46790182-46790232	Hepatocyte	liver:	n/a
49	chr3:46742898-46742948	AG09319	gingival:	n/a
50	chr3:46792023-46792073	PANC-1	pancreas:	n/a

(count:157 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:46746470..46747089-chr3:46944228..46945196,2	K562	blood:
2	chr3:46709508..46711743-chr3:46776427..46778541,2	K562	blood:
3	chr3:46650273..46651172-chr3:46707945..46708857,6	MCF-7	breast:
4	chr3:46589952..46592593-chr3:46732036..46734467,2	K562	blood:
5	chr3:46732167..46733968-chr3:46737534..46740232,2	MCF-7	breast:
6	chr3:46761792..46767256-chr3:46770894..46774909,6	K562	blood:
7	chr3:46739910..46741419-chr3:46753549..46755761,2	MCF-7	breast:
8	chr3:46723220..46725442-chr3:46727287..46728789,2	K562	blood:
9	chr3:46734848..46735671-chr3:160283077..160283853,2	Hela-S3	cervix:
10	chr3:46745129..46746095-chr3:46936433..46937176,2	MCF-7	breast:
11	chr3:46707530..46709982-chr3:46711149..46714588,3	K562	blood:
12	chr3:46722742..46724325-chr3:46733459..46735116,2	K562	blood:
13	chr3:46707418..46709371-chr3:46712225..46713806,2	K562	blood:
14	chr3:46720300..46721832-chr3:46725360..46727686,2	K562	blood:
15	chr3:46704379..46706248-chr3:46709727..46711417,3	K562	blood:
16	chr3:46722742..46724325-chr3:46733459..46735116,2	K562	blood:
17	chr3:46763658..46765267-chr3:46926020..46928200,2	MCF-7	breast:
18	chr3:46724809..46726431-chr3:46731600..46733617,2	K562	blood:
19	chr3:46746166..46747117-chr3:46950364..46951554,3	MCF-7	breast:
20	chr3:46776204..46778019-chr3:46778181..46780158,2	K562	blood:
21	chr3:46713668..46715350-chr3:46724195..46726906,2	MCF-7	breast:
22	chr3:46707887..46708803-chr3:46920018..46920840,3	MCF-7	breast:
23	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
24	chr3:46699829..46702382-chr3:46705244..46707445,2	K562	blood:
25	chr3:46476162..46478897-chr3:46745088..46748069,2	K562	blood:
26	chr3:46746189..46747162-chr3:46936459..46937309,7	MCF-7	breast:
27	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
28	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
29	chr17:43393907..43394635-chr3:46734362..46735110,2	Hela-S3	cervix:
30	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
31	chr3:46737124..46738860-chr3:46743430..46745835,2	K562	blood:
32	chr3:46717709..46719534-chr3:46734745..46736639,2	MCF-7	breast:
33	chr3:46703743..46706705-chr3:46719567..46721829,2	K562	blood:
34	chr3:46733775..46736386-chr3:46933231..46935509,2	MCF-7	breast:
35	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
36	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
37	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
38	chr3:46746279..46747291-chr3:46951057..46951891,3	MCF-7	breast:
39	chr3:46728002..46730865-chr3:46732714..46734493,2	K562	blood:
40	chr3:46724809..46726431-chr3:46731600..46733617,2	K562	blood:
41	chr3:46720846..46722573-chr3:46724433..46726635,2	MCF-7	breast:
42	chr3:46733050..46735013-chr3:46736523..46739104,3	K562	blood:
43	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
44	chr3:46738781..46740669-chr3:46750489..46752316,2	K562	blood:
45	chr3:46675056..46675850-chr3:46708207..46708731,2	MCF-7	breast:
46	chr3:46770529..46772210-chr3:46784902..46786498,2	K562	blood:
47	chr3:46729839..46731563-chr3:46733561..46736406,2	MCF-7	breast:
48	chr3:46747343..46747876-chr3:47412441..47413259,2	MCF-7	breast:
49	chr3:46736001..46738313-chr3:46739420..46741660,3	MCF-7	breast:
50	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46797532-46798119	NONHSAT089457
2	lnc-PRSS50-1	chr3:46795974-46796138	NONHSAT089457
3	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
TMIE	TF binding region
PRSS50	TF binding region
ALS2CL	TF binding region
PRSS44	TF binding region
PRSS45	TF binding region
PRSS46	TF binding region
ENSG00000238013	CpG island
TMIE	CpG island
PRSS50	CpG island
ALS2CL	CpG island
PRSS44	CpG island
PRSS45	CpG island
PRSS46	CpG island
ENSG00000270006	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000113558	chromatin interactions
ENSG00000229320	chromatin interactions
ENSG00000260456	chromatin interactions
ENSG00000006062	chromatin interactions
ENSG00000206549	chromatin interactions
ENSG00000181585	chromatin interactions
ENSG00000160799	chromatin interactions
ENSG00000160796	chromatin interactions
ENSG00000188086	chromatin interactions
ENSG00000264306	chromatin interactions
ENSG00000160801	chromatin interactions
ENSG00000261603	chromatin interactions
ENSG00000186432	chromatin interactions
ENSG00000101558	chromatin interactions
ENSG00000178038	chromatin interactions

Extended variants
information (count: 4408 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:4408 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149983776	chr3:46706596-46706597	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs571223732	chr3:46706645-46706646	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145391301	chr3:46706652-46706653	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs939420	chr3:46706685-46706686	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs561519418	chr3:46706712-46706713	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184618219	chr3:46706713-46706714	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370485020	chr3:46706753-46706754	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs386396550	chr3:46706760-46706761	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs5848807	chr3:46706766-46706767	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531841443	chr3:46706855-46706856	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550447678	chr3:46706879-46706880	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540240771	chr3:46706915-46706916	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs77167271	chr3:46706933-46706934	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs4683262	chr3:46706954-46706955	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs372523957	chr3:46706971-46706972	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs4683263	chr3:46706985-46706986	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs566099794	chr3:46706990-46706991	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144806221	chr3:46707008-46707009	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs189236222	chr3:46707033-46707034	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs576320578	chr3:46707037-46707038	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs147937518	chr3:46707042-46707043	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537689554	chr3:46707093-46707094	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556028147	chr3:46707107-46707108	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs386660746	chr3:46707112-46707113	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73831180	chr3:46707113-46707114	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs34438488	chr3:46707124-46707125	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs76125513	chr3:46707126-46707127	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542687124	chr3:46707127-46707128	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs560868250	chr3:46707132-46707133	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4683265	chr3:46707196-46707197	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs546949969	chr3:46707202-46707203	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543993608	chr3:46707209-46707210	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139912817	chr3:46707221-46707222	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565482613	chr3:46707224-46707225	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115211866	chr3:46707229-46707230	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs115876504	chr3:46707241-46707242	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs540548539	chr3:46707243-46707244	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs17079122	chr3:46707244-46707245	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs41320545	chr3:46707322-46707323	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537559616	chr3:46707359-46707360	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141225665	chr3:46707364-46707365	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143519891	chr3:46707377-46707378	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs79632122	chr3:46707445-46707446	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs193227204	chr3:46707508-46707509	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73079572	chr3:46707531-46707532	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs113717731	chr3:46707587-46707588	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs55672827	chr3:46707645-46707646	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554560524	chr3:46707646-46707647	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs372535309	chr3:46707661-46707662	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs185585629	chr3:46707673-46707674	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1975 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46698000-46707600	Weak transcription	Gastric	stomach
2	chr3:46700800-46710400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr3:46701600-46706800	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr3:46701600-46709200	Enhancers	Right Ventricle	heart
5	chr3:46702800-46707200	Weak transcription	Pancreas	Pancrea
6	chr3:46702800-46732400	Weak transcription	Psoas Muscle	Psoas
7	chr3:46703000-46711600	Weak transcription	Esophagus	oesophagus
8	chr3:46703000-46731600	Weak transcription	Hela-S3	cervix
9	chr3:46703400-46707200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr3:46703400-46709400	Enhancers	Left Ventricle	heart
11	chr3:46703800-46709200	Enhancers	Right Atrium	heart
12	chr3:46704200-46708800	Enhancers	Fetal Heart	heart
13	chr3:46704200-46712400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr3:46705000-46711400	Weak transcription	HMEC	breast
15	chr3:46705200-46708600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:46705400-46707200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr3:46705400-46707400	Weak transcription	Brain Substantia Nigra	brain
18	chr3:46705400-46707600	Weak transcription	Fetal Intestine Small	intestine
19	chr3:46705400-46711800	Weak transcription	Adipose Nuclei	Adipose
20	chr3:46705400-46711800	Weak transcription	Placenta	Placenta
21	chr3:46705400-46712400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr3:46705400-46713400	Weak transcription	Colonic Mucosa	Colon
23	chr3:46705400-46715000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:46705400-46732600	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr3:46705400-46734400	Weak transcription	Ovary	ovary
26	chr3:46705600-46710800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr3:46705800-46707800	Bivalent Enhancer	Fetal Muscle Leg	muscle
28	chr3:46705800-46714600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr3:46705800-46714800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr3:46705800-46717000	Weak transcription	Brain Anterior Caudate	brain
31	chr3:46706000-46707200	Weak transcription	Fetal Intestine Large	intestine
32	chr3:46706000-46717400	Weak transcription	Brain Angular Gyrus	brain
33	chr3:46706200-46706800	Enhancers	Liver	Liver
34	chr3:46706200-46708000	Weak transcription	Lung	lung
35	chr3:46706200-46709200	Weak transcription	Spleen	Spleen
36	chr3:46706400-46706600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr3:46706400-46708000	Weak transcription	HSMMtube	muscle
38	chr3:46706800-46707200	Weak transcription	Liver	Liver
39	chr3:46706800-46712200	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr3:46707200-46707400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr3:46707200-46708000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr3:46707200-46709000	Enhancers	Liver	Liver
43	chr3:46707200-46709200	Enhancers	Pancreas	Pancrea
44	chr3:46707200-46710800	Enhancers	Fetal Intestine Large	intestine
45	chr3:46707200-46717000	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr3:46707600-46707800	Enhancers	Brain Substantia Nigra	brain
47	chr3:46707600-46707800	Genic enhancers	Fetal Intestine Small	intestine
48	chr3:46707600-46708000	Enhancers	Stomach Smooth Muscle	stomach
49	chr3:46707600-46708600	Enhancers	Colon Smooth Muscle	Colon
50	chr3:46707600-46709000	Enhancers	Gastric	stomach

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