Variant report

Variant	nsv1058882
Chromosome Location	chr20:52765979-52794372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:839)
CpG islands
(count:976)
Chromatin interactive
region (count:175)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:52765458-52765984	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:52785754-52786208	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:52794004-52794266	HepG2	liver:	n/a	n/a
4	ATF3	chr20:52765344-52766021	A549	lung:	n/a	n/a
5	ATF3	chr20:52785452-52791659	A549	lung:	n/a	chr20:52786114-52786124
6	ATF3	chr20:52785511-52786430	A549	lung:	n/a	chr20:52786114-52786124
7	ATF3	chr20:52768165-52769587	A549	lung:	n/a	n/a
8	ATF3	chr20:52784334-52785014	A549	lung:	n/a	n/a
9	ATF3	chr20:52780601-52781481	A549	lung:	n/a	n/a
10	ATF3	chr20:52770849-52771447	A549	lung:	n/a	n/a
11	ATF3	chr20:52772261-52775274	A549	lung:	n/a	n/a
12	ATF3	chr20:52767042-52769917	A549	lung:	n/a	n/a
13	ATF3	chr20:52781513-52784169	A549	lung:	n/a	chr20:52782584-52782598
14	ATF3	chr20:52776184-52780419	A549	lung:	n/a	n/a
15	ATF3	chr20:52788358-52791066	A549	lung:	n/a	n/a
16	ATF3	chr20:52783560-52784157	A549	lung:	n/a	n/a
17	ATF3	chr20:52765351-52766004	A549	lung:	n/a	n/a
18	ATF3	chr20:52784248-52785237	A549	lung:	n/a	n/a
19	BACH1	chr20:52789290-52789655	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr20:52789866-52789951	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr20:52774777-52775850	A549	lung:	n/a	n/a
22	BCL3	chr20:52770271-52771442	A549	lung:	n/a	n/a
23	BCL3	chr20:52764999-52772113	A549	lung:	n/a	chr20:52769068-52769077
24	BCL3	chr20:52785315-52791512	A549	lung:	n/a	chr20:52790491-52790504 chr20:52790858-52790871 chr20:52790857-52790870
25	BCL3	chr20:52784264-52785294	A549	lung:	n/a	chr20:52784755-52784763
26	BCL3	chr20:52776372-52780600	A549	lung:	n/a	n/a
27	BCL3	chr20:52780648-52781324	A549	lung:	n/a	n/a
28	BCL3	chr20:52783474-52784095	A549	lung:	n/a	n/a
29	BCL3	chr20:52765237-52769922	A549	lung:	n/a	chr20:52769068-52769077
30	BCL3	chr20:52772170-52791941	A549	lung:	n/a	chr20:52790491-52790504 chr20:52782584-52782593 chr20:52784755-52784763 chr20:52790858-52790871 chr20:52790857-52790870 chr20:52782583-52782592
31	BCL3	chr20:52772378-52774672	A549	lung:	n/a	n/a
32	BCL3	chr20:52782056-52783254	A549	lung:	n/a	chr20:52782584-52782593 chr20:52782583-52782592
33	BHLHE40	chr20:52778052-52778331	HepG2	liver:	n/a	n/a
34	BRCA1	chr20:52765503-52766014	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr20:52785585-52786400	HCT-116	colon:	n/a	n/a
36	CBX3	chr20:52765327-52766394	HCT-116	colon:	n/a	n/a
37	CBX3	chr20:52784224-52785298	HCT-116	colon:	n/a	n/a
38	CBX3	chr20:52793096-52793650	HCT-116	colon:	n/a	n/a
39	CEBPB	chr20:52771526-52772282	A549	lung:	n/a	n/a
40	CEBPB	chr20:52770398-52771133	A549	lung:	n/a	chr20:52770665-52770676
41	CEBPB	chr20:52768357-52769832	A549	lung:	n/a	chr20:52769805-52769816 chr20:52769805-52769818 chr20:52769805-52769816
42	CEBPB	chr20:52790710-52791071	IMR90	lung:	n/a	chr20:52790886-52790897
43	CEBPB	chr20:52784282-52785144	A549	lung:	n/a	n/a
44	CEBPB	chr20:52790598-52791080	H1-hESC	embryonic stem cell:	n/a	chr20:52790886-52790897
45	CEBPB	chr20:52790327-52791796	A549	lung:	n/a	chr20:52790886-52790897
46	CEBPB	chr20:52792987-52793766	HCT-116	colon:	n/a	n/a
47	CEBPB	chr20:52765239-52766630	A549	lung:	n/a	n/a
48	CEBPB	chr20:52790743-52791016	HepG2	liver:	n/a	chr20:52790886-52790897
49	CEBPB	chr20:52790409-52791771	HCT-116	colon:	n/a	chr20:52790886-52790897
50	CEBPB	chr20:52785756-52787112	A549	lung:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:52781187-52781237	BJ	skin:	n/a
2	chr20:52790139-52790189	T-47D	breast:	n/a
3	chr20:52788779-52788829	HEK293	kidney:	embryo
4	chr20:52790712-52790762	PFSK-1	brain:	n/a
5	chr20:52790141-52790191	MCF-7	breast:	n/a
6	chr20:52789956-52790006	HMEC	breast:	n/a
7	chr20:52781187-52781237	Hepatocyte	liver:	n/a
8	chr20:52786323-52786373	AG10803	skin:	n/a
9	chr20:52790139-52790189	MCF-7	breast:	n/a
10	chr20:52789646-52789696	NH-A	brain:	n/a
11	chr20:52791472-52791522	ovcar-3	ovarian:	n/a
12	chr20:52791472-52791522	GM12891	blood:	n/a
13	chr20:52790139-52790189	MCF10A-Er-Src	breast:	n/a
14	chr20:52790063-52790113	Hela-S3	cervix:	n/a
15	chr20:52793130-52793180	K562	blood:	n/a
16	chr20:52790601-52790651	GM12891	blood:	n/a
17	chr20:52790141-52790191	IMR90	lung:	fetal
18	chr20:52789956-52790006	HUVEC	blood vessel:	n/a
19	chr20:52791472-52791522	GM12878	blood:	n/a
20	chr20:52786323-52786373	Hela-S3	cervix:	n/a
21	chr20:52788779-52788829	HCPEpiC	choroid plexus:	n/a
22	chr20:52790733-52790783	HCF	heart:	n/a
23	chr20:52770785-52770835	HCT-116	colon:	n/a
24	chr20:52791472-52791522	NT2-D1	testis:	n/a
25	chr20:52790978-52791028	T-47D	breast:	n/a
26	chr20:52791472-52791522	HEEpiC	esophagus:	n/a
27	chr20:52770785-52770835	HRE	kidney:	n/a
28	chr20:52791472-52791522	GM12892	blood:	n/a
29	chr20:52790733-52790783	HUVEC	blood vessel:	n/a
30	chr20:52788779-52788829	HepG2	liver:	n/a
31	chr20:52788779-52788829	MCF-7	breast:	n/a
32	chr20:52790712-52790762	SK-N-MC	brain:	n/a
33	chr20:52790712-52790762	HRPEpiC	eye:	n/a
34	chr20:52788779-52788829	HCM	heart:	n/a
35	chr20:52790978-52791028	GM12878	blood:	n/a
36	chr20:52793130-52793180	GM12878	blood:	n/a
37	chr20:52790712-52790762	HIPEpiC	eye:	n/a
38	chr20:52790063-52790113	SAEC	small airway:	n/a
39	chr20:52790733-52790783	U87	brain:	n/a
40	chr20:52793130-52793180	NHDF-neo	bronchial:	n/a
41	chr20:52791472-52791522	PrEC	prostate:	n/a
42	chr20:52790589-52790639	BE2_C	brain:	n/a
43	chr20:52788779-52788829	H1-hESC	embryonic stem cell:	embryo
44	chr20:52770785-52770835	HRPEpiC	eye:	n/a
45	chr20:52790712-52790762	Hepatocyte	liver:	n/a
46	chr20:52793130-52793180	ECC-1	luminal epithelium:	n/a
47	chr20:52789646-52789696	HRE	kidney:	n/a
48	chr20:52790601-52790651	LNCaP	prostate:	n/a
49	chr20:52790141-52790191	Jurkat	blood:	n/a
50	chr20:52790141-52790191	RPTEC	kidney:	n/a

(count:175 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr20:52772070..52772872-chr20:52786707..52787281,2	MCF-7	breast:
2	chr20:52747406..52750042-chr20:52765504..52767989,2	K562	blood:
3	chr10:61594823..61595369-chr20:52765425..52766238,2	MCF-7	breast:
4	chr20:52739905..52740841-chr20:52768331..52768949,5	MCF-7	breast:
5	chr20:52765145..52766456-chr20:52811076..52812871,393	MCF-7	breast:
6	chr20:52599220..52600148-chr20:52765356..52766212,6	MCF-7	breast:
7	chr20:52743212..52744202-chr20:52765089..52766236,3	MCF-7	breast:
8	chr20:52748821..52749601-chr20:52765286..52765999,2	MCF-7	breast:
9	chr20:46704502..46705337-chr20:52765426..52766199,4	MCF-7	breast:
10	chr17:57920588..57922273-chr20:52783196..52786191,2	MCF-7	breast:
11	chr17:59800505..59801023-chr20:52765436..52766226,2	MCF-7	breast:
12	chr17:56734965..56736962-chr20:52770464..52773250,2	MCF-7	breast:
13	chr20:52789239..52792588-chr20:55839235..55841581,3	MCF-7	breast:
14	chr17:56735473..56737837-chr20:52789493..52791187,2	MCF-7	breast:
15	chr20:46413516..46416980-chr20:52787199..52790705,5	MCF-7	breast:
16	chr20:52765302..52766219-chr20:52784081..52784986,2	MCF-7	breast:
17	chr17:56707725..56710299-chr20:52776284..52779199,4	MCF-7	breast:
18	chr20:52791642..52795116-chr20:52796704..52799912,3	K562	blood:
19	chr20:52768317..52770399-chr20:52774857..52777374,2	K562	blood:
20	chr20:52740259..52740856-chr20:52768240..52768937,2	MCF-7	breast:
21	chr20:52793616..52795896-chr20:52798074..52799912,2	K562	blood:
22	chr20:52765344..52766249-chr7:107591882..107592609,3	MCF-7	breast:
23	chr20:52765013..52767443-chr20:55839272..55842153,3	MCF-7	breast:
24	chr17:56728473..56731849-chr20:52782841..52785983,3	MCF-7	breast:
25	chr17:56735044..56737972-chr20:52763206..52766874,4	MCF-7	breast:
26	chr19:34268813..34269362-chr20:52771784..52772475,2	MCF-7	breast:
27	chr20:52701305..52702094-chr20:52765727..52766247,2	MCF-7	breast:
28	chr20:52726502..52727236-chr20:52765507..52766051,3	MCF-7	breast:
29	chr20:52703317..52704240-chr20:52765410..52766285,3	MCF-7	breast:
30	chr20:52743107..52744370-chr20:52765246..52766112,8	MCF-7	breast:
31	chr14:95288063..95290182-chr20:52767433..52769417,2	MCF-7	breast:
32	chr17:56707655..56710702-chr20:52792867..52796223,6	MCF-7	breast:
33	chr20:52720353..52721347-chr20:52765343..52766302,16	MCF-7	breast:
34	chr17:56735121..56737644-chr20:52779183..52780879,2	MCF-7	breast:
35	chr12:76423841..76426201-chr20:52778674..52781449,2	MCF-7	breast:
36	chr1:149858452..149860171-chr20:52780494..52782390,2	MCF-7	breast:
37	chr20:52784393..52784975-chr20:52811607..52812127,2	MCF-7	breast:
38	chr20:52765499..52766221-chr3:64598795..64599626,3	MCF-7	breast:
39	chr17:56707293..56709240-chr20:52784800..52786462,3	MCF-7	breast:
40	chr20:52739732..52740989-chr20:52765195..52766259,18	MCF-7	breast:
41	chr20:52768122..52769040-chr20:52811641..52812560,3	MCF-7	breast:
42	chr20:52768988..52769787-chr20:52779061..52780220,3	MCF-7	breast:
43	chr20:52765182..52766890-chr20:52811098..52812679,34	MCF-7	breast:
44	chr20:52765381..52766270-chr20:52885301..52885922,2	MCF-7	breast:
45	chr20:52765397..52766265-chr3:61613482..61614028,2	MCF-7	breast:
46	chr20:52765064..52766063-chr20:52814244..52815054,2	MCF-7	breast:
47	chr17:57917132..57919949-chr20:52788043..52790294,2	MCF-7	breast:
48	chr20:52765274..52766299-chr20:55837767..55838761,6	MCF-7	breast:
49	chr20:41007695..41010681-chr20:52764867..52766401,2	MCF-7	breast:
50	chr20:45984855..45987152-chr20:52768501..52771128,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CYP24A1	hsa-miR-26b-5p	chr20:52770528-52770547
2	CYP24A1	hsa-miR-125b-5p	chr20:52773677-52773670
3	CYP24A1	hsa-miR-125b-5p	chr20:52771264-52771285

Variant related genes	Relation type
CYP24A1	TF binding region
CYP24A1	CpG island
ENSG00000199004	chromatin interactions
ENSG00000095066	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000185453	chromatin interactions
ENSG00000105486	chromatin interactions
ENSG00000101138	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000257453	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000171223	chromatin interactions
ENSG00000235415	chromatin interactions
ENSG00000198518	chromatin interactions
ENSG00000196562	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000103260	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000232638	chromatin interactions
ENSG00000203499	chromatin interactions
ENSG00000091136	chromatin interactions
ENSG00000179743	chromatin interactions
ENSG00000266826	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000121060	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000139289	chromatin interactions
ENSG00000087586	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 1323 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1323 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16999037	chr20:52765979-52765980	Enhancers Weak transcription	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78801370	chr20:52766066-52766067	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs35749422	chr20:52766070-52766071	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs2762928	chr20:52766085-52766086	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs374525168	chr20:52766089-52766090	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs376351912	chr20:52766090-52766091	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs576599624	chr20:52766108-52766109	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs183726030	chr20:52766171-52766172	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs2762929	chr20:52766195-52766196	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs570543380	chr20:52766220-52766221	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs188959937	chr20:52766238-52766239	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs541487671	chr20:52766246-52766247	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs66870448	chr20:52766340-52766341	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs141757936	chr20:52766349-52766350	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs8118441	chr20:52766385-52766386	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs570017670	chr20:52766408-52766409	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs531565789	chr20:52766416-52766417	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs548056967	chr20:52766459-52766460	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs533280184	chr20:52766513-52766514	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs547029794	chr20:52766518-52766519	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs146030482	chr20:52766519-52766520	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs568387566	chr20:52766528-52766529	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs147104141	chr20:52766580-52766581	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs539424010	chr20:52766599-52766600	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs570115524	chr20:52766625-52766626	Weak transcription Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs539017565	chr20:52766717-52766718	Weak transcription Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs73912628	chr20:52766744-52766745	Weak transcription Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs556241320	chr20:52766765-52766766	Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs193132413	chr20:52766799-52766800	Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs542439018	chr20:52766801-52766802	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs8124792	chr20:52766807-52766808	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs572819817	chr20:52766833-52766834	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs541758092	chr20:52766897-52766898	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs2762930	chr20:52766911-52766912	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533387608	chr20:52766925-52766926	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs113173286	chr20:52766941-52766942	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs368042052	chr20:52766942-52766943	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs11477913	chr20:52766960-52766961	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs543821587	chr20:52767116-52767117	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs563831197	chr20:52767150-52767151	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs147756491	chr20:52767154-52767155	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs34194258	chr20:52767170-52767171	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs371672960	chr20:52767197-52767198	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs6013903	chr20:52767203-52767204	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs554690887	chr20:52767234-52767235	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs149131997	chr20:52767286-52767287	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs569557010	chr20:52767343-52767344	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs376782707	chr20:52767349-52767350	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs183585332	chr20:52767428-52767429	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs6097801	chr20:52767434-52767435	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:82)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myelodysplastic syndrome	21251322	CNVD
Ductal carcinoma	22052326	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
Ovarian cancer	22174824	CNVD
Lung cancer	16740712	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16620391	CNVD
Okamoto syndrome	17623483	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Cervical cancer	16585170	CNVD
Ovarian cancer	20844748	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20459607	CNVD
Gastric cancer	18160780	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52758600-52768800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:52764800-52766400	Enhancers	HepG2	liver
3	chr20:52764800-52766600	Enhancers	Hela-S3	cervix
4	chr20:52765400-52766400	Enhancers	Fetal Intestine Large	intestine
5	chr20:52765400-52766600	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr20:52765600-52766000	Enhancers	A549	lung
7	chr20:52765600-52766000	Enhancers	NHEK	skin
8	chr20:52765600-52766400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr20:52765600-52766400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr20:52765800-52766400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr20:52765800-52766400	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr20:52765800-52768400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr20:52766000-52766800	Flanking Active TSS	A549	lung
14	chr20:52766000-52768800	Weak transcription	NHEK	skin
15	chr20:52766200-52766400	Bivalent Enhancer	Small Intestine	intestine
16	chr20:52766400-52768600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr20:52766400-52768800	Weak transcription	HepG2	liver
18	chr20:52766800-52768600	Enhancers	A549	lung
19	chr20:52767000-52768000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr20:52768000-52768200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
21	chr20:52768200-52769400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr20:52768400-52768800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr20:52768400-52769800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr20:52768600-52768800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr20:52768600-52768800	Genic enhancers	A549	lung
26	chr20:52768600-52768800	Enhancers	Osteobl	bone
27	chr20:52768600-52769000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr20:52768600-52769200	Enhancers	Esophagus	oesophagus
29	chr20:52768600-52769800	Enhancers	HMEC	breast
30	chr20:52768800-52769000	Flanking Active TSS	Osteobl	bone
31	chr20:52768800-52769200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr20:52768800-52769400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr20:52768800-52769400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr20:52768800-52769400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr20:52768800-52769400	Flanking Active TSS	NHEK	skin
36	chr20:52768800-52769600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr20:52768800-52769800	Enhancers	HepG2	liver
38	chr20:52768800-52790200	Transcr. at gene 5' and 3'	A549	lung
39	chr20:52769000-52769200	Active TSS	Osteobl	bone
40	chr20:52769000-52769400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr20:52769000-52769400	Enhancers	Left Ventricle	heart
42	chr20:52769000-52769600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr20:52769000-52769800	Enhancers	Placenta	Placenta
44	chr20:52769200-52769400	Flanking Active TSS	Osteobl	bone
45	chr20:52769200-52769600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr20:52769200-52789400	Weak transcription	Esophagus	oesophagus
47	chr20:52769400-52769600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr20:52769400-52769600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr20:52769400-52769800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr20:52769400-52769800	Enhancers	NHEK	skin

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