Variant report

Variant	esv1797503
Chromosome Location	chr3:46708712-46760713
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1574)
CpG islands
(count:2936)
Chromatin interactive
region (count:111)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1574 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:46755533-46755773	GM12878	blood:	n/a	n/a
2	ATF2	chr3:46746461-46746813	GM12878	blood:	n/a	n/a
3	ATF2	chr3:46755483-46755920	GM12878	blood:	n/a	n/a
4	ATF2	chr3:46759302-46759627	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr3:46759331-46759550	H1-hESC	embryonic stem cell:	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	BACH1	chr3:46734048-46734515	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr3:46735430-46735744	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:46759334-46759543	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:46746558-46746758	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr3:46720127-46720375	GM12878	blood:	n/a	n/a
13	BATF	chr3:46755589-46755797	GM12878	blood:	n/a	n/a
14	BATF	chr3:46720130-46720422	GM12878	blood:	n/a	n/a
15	BATF	chr3:46755501-46755889	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:46755446-46755860	GM12878	blood:	n/a	chr3:46755588-46755601
17	BCL11A	chr3:46755551-46755755	GM12878	blood:	n/a	chr3:46755588-46755601
18	BCL3	chr3:46755447-46755829	GM12878	blood:	n/a	chr3:46755588-46755601
19	BCLAF1	chr3:46759179-46759647	K562	blood:	n/a	n/a
20	BHLHE40	chr3:46735446-46735593	K562	blood:	n/a	n/a
21	BHLHE40	chr3:46734263-46734269	A549	lung:	n/a	n/a
22	BHLHE40	chr3:46734493-46734748	K562	blood:	n/a	n/a
23	BHLHE40	chr3:46736761-46737392	K562	blood:	n/a	n/a
24	BHLHE40	chr3:46746528-46746852	K562	blood:	n/a	n/a
25	BHLHE40	chr3:46755577-46755866	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:46736984-46737365	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:46759435-46759439	K562	blood:	n/a	n/a
28	BRCA1	chr3:46759337-46759615	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr3:46746485-46746854	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr3:46708976-46709045	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr3:46746586-46746696	HepG2	liver:	n/a	n/a
32	BRCA1	chr3:46734876-46735076	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr3:46755567-46755723	GM12878	blood:	n/a	n/a
34	BRCA1	chr3:46746601-46746847	H1-hESC	embryonic stem cell:	n/a	n/a
35	CBX3	chr3:46759328-46759544	K562	blood:	n/a	n/a
36	CBX3	chr3:46759289-46759662	K562	blood:	n/a	n/a
37	CCNT2	chr3:46759152-46759605	K562	blood:	n/a	n/a
38	CCNT2	chr3:46734819-46735516	K562	blood:	n/a	n/a
39	CEBPB	chr3:46759364-46759565	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:46737567-46737769	K562	blood:	n/a	chr3:46737680-46737691 chr3:46737682-46737693 chr3:46737680-46737693 chr3:46737682-46737691
41	CEBPB	chr3:46746392-46746831	GM12878	blood:	n/a	n/a
42	CEBPB	chr3:46732340-46732540	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:46737527-46737719	Hela-S3	cervix:	n/a	chr3:46737680-46737691 chr3:46737682-46737693 chr3:46737680-46737693 chr3:46737682-46737691
44	CEBPB	chr3:46737591-46737781	HepG2	liver:	n/a	chr3:46737680-46737691 chr3:46737682-46737693 chr3:46737680-46737693 chr3:46737682-46737691
45	CEBPB	chr3:46734030-46734446	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr3:46720185-46720372	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr3:46755525-46755754	GM12878	blood:	n/a	n/a
48	CHD2	chr3:46759325-46759594	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr3:46734962-46735064	K562	blood:	n/a	n/a
50	CHD2	chr3:46746575-46746904	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2936 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46735315-46735365	HUVEC	blood vessel:	n/a
2	chr3:46718990-46719040	AG09319	gingival:	n/a
3	chr3:46742703-46742753	AG09309	skin:	n/a
4	chr3:46759096-46759146	HAEpiC	amniotic membrane:	n/a
5	chr3:46735335-46735385	AG09309	skin:	n/a
6	chr3:46718369-46718419	MCF-7	breast:	n/a
7	chr3:46735154-46735204	H1-hESC	embryonic stem cell:	embryo
8	chr3:46735335-46735385	Hela-S3	cervix:	n/a
9	chr3:46735315-46735365	HUVEC	blood vessel:	n/a
10	chr3:46718990-46719040	AG09319	gingival:	n/a
11	chr3:46742703-46742753	AG09309	skin:	n/a
12	chr3:46759096-46759146	HAEpiC	amniotic membrane:	n/a
13	chr3:46735335-46735385	AG09309	skin:	n/a
14	chr3:46718369-46718419	MCF-7	breast:	n/a
15	chr3:46735154-46735204	H1-hESC	embryonic stem cell:	embryo
16	chr3:46735335-46735385	Hela-S3	cervix:	n/a
17	chr3:46735154-46735204	HRPEpiC	eye:	n/a
18	chr3:46759472-46759522	IMR90	lung:	fetal
19	chr3:46735315-46735365	AG09319	gingival:	n/a
20	chr3:46735009-46735059	ECC-1	luminal epithelium:	n/a
21	chr3:46733475-46733525	HCF	heart:	n/a
22	chr3:46741803-46741853	HMEC	breast:	n/a
23	chr3:46759449-46759499	U87	brain:	n/a
24	chr3:46735315-46735365	HepG2	liver:	n/a
25	chr3:46759335-46759385	CMK	blood:	n/a
26	chr3:46759472-46759522	U87	brain:	n/a
27	chr3:46743078-46743128	HL-60	blood:	n/a
28	chr3:46743078-46743128	GM19239	blood:	n/a
29	chr3:46759588-46759638	AG09309	skin:	n/a
30	chr3:46759588-46759638	T-47D	breast:	n/a
31	chr3:46735335-46735385	Hepatocyte	liver:	n/a
32	chr3:46718369-46718419	HMEC	breast:	n/a
33	chr3:46747930-46747980	LNCaP	prostate:	n/a
34	chr3:46743199-46743249	BE2_C	brain:	n/a
35	chr3:46741803-46741853	K562	blood:	n/a
36	chr3:46739004-46739054	LNCaP	prostate:	n/a
37	chr3:46734393-46734443	ECC-1	luminal epithelium:	n/a
38	chr3:46755916-46755966	K562	blood:	n/a
39	chr3:46719625-46719675	MCF-7	breast:	n/a
40	chr3:46734393-46734443	HAEpiC	amniotic membrane:	n/a
41	chr3:46735315-46735365	HAEpiC	amniotic membrane:	n/a
42	chr3:46735454-46735504	Hepatocyte	liver:	n/a
43	chr3:46759438-46759488	AG09319	gingival:	n/a
44	chr3:46718990-46719040	AG04449	skin:	fetal
45	chr3:46734393-46734443	HCM	heart:	n/a
46	chr3:46759656-46759706	HUVEC	blood vessel:	n/a
47	chr3:46742865-46742915	GM19239	blood:	n/a
48	chr3:46759588-46759638	AoSMC	blood vessel:	n/a
49	chr3:46742491-46742541	AG04450	lung:	fetal
50	chr3:46759335-46759385	Hepatocyte	liver:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
2	chr3:46746174..46747036-chr3:46933635..46934581,2	MCF-7	breast:
3	chr3:46476162..46478897-chr3:46745088..46748069,2	K562	blood:
4	chr3:46707418..46709371-chr3:46712225..46713806,2	K562	blood:
5	chr3:46724809..46726431-chr3:46731600..46733617,2	K562	blood:
6	chr3:46735288..46735975-chr3:46746178..46746698,2	K562	blood:
7	chr3:46729839..46731563-chr3:46733561..46736406,2	MCF-7	breast:
8	chr3:46734848..46735671-chr3:160283077..160283853,2	Hela-S3	cervix:
9	chr3:46589952..46592593-chr3:46732036..46734467,2	K562	blood:
10	chr3:46720300..46721832-chr3:46725360..46727686,2	K562	blood:
11	chr3:46734988..46739707-chr3:46741491..46746249,8	K562	blood:
12	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
13	chr3:46703608..46706840-chr3:46708905..46711367,3	K562	blood:
14	chr3:46751310..46753575-chr3:46950623..46952874,2	K562	blood:
15	chr3:46747343..46747876-chr3:47412441..47413259,2	MCF-7	breast:
16	chr3:46713668..46715350-chr3:46724195..46726906,2	MCF-7	breast:
17	chr3:46738781..46740669-chr3:46750489..46752316,2	K562	blood:
18	chr3:46728002..46730865-chr3:46732714..46734493,2	K562	blood:
19	chr3:46746240..46747607-chr3:46936343..46937490,8	K562	blood:
20	chr3:46748228..46751973-chr3:46757589..46759527,3	MCF-7	breast:
21	chr3:46708885..46711230-chr3:46720885..46722743,2	K562	blood:
22	chr3:46675056..46675850-chr3:46708207..46708731,2	MCF-7	breast:
23	chr3:46706471..46710183-chr3:46732042..46737071,8	MCF-7	breast:
24	chr3:46746540..46747094-chr3:46948369..46948995,2	K562	blood:
25	chr3:46737124..46738860-chr3:46743430..46745835,2	K562	blood:
26	chr3:46737124..46738860-chr3:46743430..46745835,2	K562	blood:
27	chr3:46733404..46735141-chr3:46748725..46750536,2	MCF-7	breast:
28	chr3:46733050..46735013-chr3:46736523..46739104,3	K562	blood:
29	chr3:46711200..46713596-chr3:46721127..46724340,3	MCF-7	breast:
30	chr3:46723220..46725442-chr3:46727287..46728789,2	K562	blood:
31	chr3:46720266..46726397-chr3:46730234..46736031,11	MCF-7	breast:
32	chr3:46743022..46745285-chr3:46747232..46748921,2	MCF-7	breast:
33	chr3:46719842..46724126-chr3:46725182..46728551,5	MCF-7	breast:
34	chr3:46732249..46733917-chr3:46887547..46889689,2	MCF-7	breast:
35	chr3:46746480..46747149-chr3:46935659..46936387,2	MCF-7	breast:
36	chr3:46723220..46725442-chr3:46727287..46728789,2	K562	blood:
37	chr3:46709508..46711743-chr3:46776427..46778541,2	K562	blood:
38	chr3:46733775..46736386-chr3:46933231..46935509,2	MCF-7	breast:
39	chr3:46710631..46712822-chr3:46733923..46736915,2	MCF-7	breast:
40	chr3:46739910..46741419-chr3:46753549..46755761,2	MCF-7	breast:
41	chr3:46711200..46713596-chr3:46721127..46724340,3	MCF-7	breast:
42	chr3:46738781..46740669-chr3:46750489..46752316,2	K562	blood:
43	chr3:46746189..46747162-chr3:46936459..46937309,7	MCF-7	breast:
44	chr1:145382730..145383465-chr3:46734207..46734831,2	Hela-S3	cervix:
45	chr3:46720846..46722573-chr3:46724433..46726635,2	MCF-7	breast:
46	chr3:46727228..46728966-chr3:46733953..46736309,2	MCF-7	breast:
47	chr3:46734355..46735316-chr5:133512715..133513418,2	Hela-S3	cervix:
48	chr3:46702436..46704815-chr3:46735975..46737913,2	MCF-7	breast:
49	chr3:46727378..46730139-chr3:46733383..46735627,3	MCF-7	breast:
50	chr3:46742077..46744445-chr3:46744916..46748199,4	K562	blood:

No data

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

Extended variants
information (count: 2289 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2289 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138741265	chr3:46708726-46708727	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141891053	chr3:46708814-46708815	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs571493113	chr3:46708826-46708827	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs6442015	chr3:46708865-46708866	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs72892110	chr3:46708884-46708885	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs386660747	chr3:46708912-46708913	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376785276	chr3:46708914-46708915	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181748780	chr3:46708963-46708964	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570520185	chr3:46708964-46708965	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs9819415	chr3:46708987-46708988	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553260685	chr3:46709047-46709048	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs115003189	chr3:46709069-46709070	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs79817367	chr3:46709104-46709105	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
14	rs184081630	chr3:46709147-46709148	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs575227007	chr3:46709207-46709208	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545752215	chr3:46709234-46709235	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs188799828	chr3:46709254-46709255	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572973676	chr3:46709354-46709355	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs540737083	chr3:46709359-46709360	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146237329	chr3:46709387-46709388	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138067728	chr3:46709414-46709415	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs939409	chr3:46709418-46709419	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs563614190	chr3:46709430-46709431	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375388896	chr3:46709450-46709451	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs939410	chr3:46709468-46709469	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs372062390	chr3:46709476-46709477	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs939411	chr3:46709500-46709501	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs372354988	chr3:46709505-46709506	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149511823	chr3:46709544-46709545	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546706470	chr3:46709588-46709589	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554218622	chr3:46709622-46709623	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs540676104	chr3:46709626-46709627	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs181321258	chr3:46709646-46709647	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs536088957	chr3:46709654-46709655	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs71327086	chr3:46709657-46709658	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs4683267	chr3:46709661-46709662	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs144706370	chr3:46709747-46709748	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs185963483	chr3:46709762-46709763	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs549624709	chr3:46709764-46709765	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs59177997	chr3:46709778-46709779	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs572936723	chr3:46709780-46709781	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs540347363	chr3:46709783-46709784	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs559102296	chr3:46709785-46709786	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs148539259	chr3:46709789-46709790	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577493152	chr3:46709827-46709828	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs114998297	chr3:46709829-46709830	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116630764	chr3:46709832-46709833	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs574857008	chr3:46709842-46709843	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs530794148	chr3:46709854-46709855	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs113087717	chr3:46709866-46709867	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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

Chromatin state (count:1656 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46700800-46710400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr3:46701600-46709200	Enhancers	Right Ventricle	heart
3	chr3:46702800-46732400	Weak transcription	Psoas Muscle	Psoas
4	chr3:46703000-46711600	Weak transcription	Esophagus	oesophagus
5	chr3:46703000-46731600	Weak transcription	Hela-S3	cervix
6	chr3:46703400-46709400	Enhancers	Left Ventricle	heart
7	chr3:46703800-46709200	Enhancers	Right Atrium	heart
8	chr3:46704200-46708800	Enhancers	Fetal Heart	heart
9	chr3:46704200-46712400	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr3:46705000-46711400	Weak transcription	HMEC	breast
11	chr3:46705400-46711800	Weak transcription	Adipose Nuclei	Adipose
12	chr3:46705400-46711800	Weak transcription	Placenta	Placenta
13	chr3:46705400-46712400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:46705400-46713400	Weak transcription	Colonic Mucosa	Colon
15	chr3:46705400-46715000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr3:46705400-46732600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr3:46705400-46734400	Weak transcription	Ovary	ovary
18	chr3:46705600-46710800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr3:46705800-46714600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:46705800-46714800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr3:46705800-46717000	Weak transcription	Brain Anterior Caudate	brain
22	chr3:46706000-46717400	Weak transcription	Brain Angular Gyrus	brain
23	chr3:46706200-46709200	Weak transcription	Spleen	Spleen
24	chr3:46706800-46712200	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr3:46707200-46709000	Enhancers	Liver	Liver
26	chr3:46707200-46709200	Enhancers	Pancreas	Pancrea
27	chr3:46707200-46710800	Enhancers	Fetal Intestine Large	intestine
28	chr3:46707200-46717000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr3:46707600-46709000	Enhancers	Gastric	stomach
30	chr3:46707800-46708800	Enhancers	Fetal Intestine Small	intestine
31	chr3:46708000-46710600	Enhancers	HSMMtube	muscle
32	chr3:46708000-46716600	Weak transcription	Stomach Smooth Muscle	stomach
33	chr3:46708000-46717200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr3:46708200-46708800	Bivalent Enhancer	Fetal Stomach	stomach
35	chr3:46708200-46709200	Bivalent Enhancer	Fetal Muscle Leg	muscle
36	chr3:46708400-46709200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr3:46708400-46709600	Weak transcription	Rectal Smooth Muscle	rectum
38	chr3:46708600-46709200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:46708600-46712000	Weak transcription	Lung	lung
40	chr3:46708800-46709200	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr3:46708800-46709800	Weak transcription	Fetal Intestine Small	intestine
42	chr3:46709000-46712000	Weak transcription	Liver	Liver
43	chr3:46709000-46712400	Weak transcription	Gastric	stomach
44	chr3:46709200-46709600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr3:46709200-46709800	Enhancers	Spleen	Spleen
46	chr3:46709200-46710000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr3:46709200-46710200	Weak transcription	Right Atrium	heart
48	chr3:46709200-46711200	Weak transcription	Right Ventricle	heart
49	chr3:46709200-46712200	Weak transcription	Pancreas	Pancrea
50	chr3:46709400-46712600	Weak transcription	Left Ventricle	heart

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