Variant report

Variant	nsv899542
Chromosome Location	chr12:117549739-117623136
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1791)
CpG islands
(count:1344)
Chromatin interactive
region (count:107)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1791 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:117592917-117593335	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:117588895-117589175	K562	blood:	n/a	n/a
3	ARID3A	chr12:117557552-117557879	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:117609399-117609663	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:117580943-117581162	HepG2	liver:	n/a	n/a
6	ATF1	chr12:117588938-117589190	K562	blood:	n/a	n/a
7	ATF2	chr12:117579928-117580272	GM12878	blood:	n/a	n/a
8	ATF2	chr12:117580858-117581319	GM12878	blood:	n/a	n/a
9	ATF2	chr12:117579843-117580375	GM12878	blood:	n/a	n/a
10	ATF2	chr12:117592963-117593401	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:117603939-117604205	GM12878	blood:	n/a	n/a
12	ATF3	chr12:117578431-117579156	A549	lung:	n/a	n/a
13	ATF3	chr12:117593079-117593299	K562	blood:	n/a	n/a
14	ATF3	chr12:117565905-117566512	K562	blood:	n/a	chr12:117566397-117566410 chr12:117566398-117566409 chr12:117566399-117566410 chr12:117566401-117566411 chr12:117566397-117566412 chr12:117566398-117566408 chr12:117566398-117566411 chr12:117566399-117566410 chr12:117566401-117566409 chr12:117566398-117566408 chr12:117566401-117566408
15	ATF3	chr12:117578446-117578982	A549	lung:	n/a	n/a
16	ATF3	chr12:117579902-117581514	A549	lung:	n/a	chr12:117581215-117581225
17	ATF3	chr12:117580531-117581419	A549	lung:	n/a	chr12:117581215-117581225
18	BACH1	chr12:117593057-117593594	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:117549184-117550070	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr12:117557549-117557885	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr12:117549506-117549877	K562	blood:	n/a	n/a
22	BACH1	chr12:117588992-117589191	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr12:117556727-117556928	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr12:117580865-117581188	GM12878	blood:	n/a	n/a
25	BATF	chr12:117618562-117618817	GM12878	blood:	n/a	chr12:117618709-117618720
26	BATF	chr12:117580836-117581143	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:117580843-117581187	GM12878	blood:	n/a	chr12:117581029-117581038
28	BCL11A	chr12:117579897-117580272	GM12878	blood:	n/a	chr12:117580115-117580124
29	BCL11A	chr12:117579919-117580233	GM12878	blood:	n/a	chr12:117580115-117580124
30	BCL11A	chr12:117580878-117581200	GM12878	blood:	n/a	chr12:117581029-117581038
31	BCL3	chr12:117578319-117579096	A549	lung:	n/a	n/a
32	BCL3	chr12:117579355-117581646	A549	lung:	n/a	chr12:117580115-117580124 chr12:117581029-117581038
33	BCL3	chr12:117552507-117552909	GM12878	blood:	n/a	n/a
34	BCL3	chr12:117578200-117579114	A549	lung:	n/a	n/a
35	BCL3	chr12:117579774-117581751	A549	lung:	n/a	chr12:117580115-117580124 chr12:117581029-117581038
36	BCLAF1	chr12:117565691-117566543	K562	blood:	n/a	n/a
37	BCLAF1	chr12:117588474-117588767	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:117565801-117566505	K562	blood:	n/a	n/a
39	BHLHE40	chr12:117579931-117580340	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:117565949-117566418	K562	blood:	n/a	n/a
41	BHLHE40	chr12:117574030-117574049	K562	blood:	n/a	n/a
42	BHLHE40	chr12:117561305-117561568	K562	blood:	n/a	n/a
43	BHLHE40	chr12:117580590-117581253	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:117580902-117581273	HepG2	liver:	n/a	n/a
45	BHLHE40	chr12:117549622-117549897	K562	blood:	n/a	n/a
46	BHLHE40	chr12:117593054-117593242	K562	blood:	n/a	chr12:117593146-117593162
47	BHLHE40	chr12:117557607-117557895	K562	blood:	n/a	n/a
48	BHLHE40	chr12:117588633-117588833	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:117588811-117589198	K562	blood:	n/a	n/a
50	BHLHE40	chr12:117580844-117581249	A549	lung:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117595820-117595870	GM12878	blood:	n/a
2	chr12:117595820-117595870	IMR90	lung:	fetal
3	chr12:117595820-117595870	GM12878	blood:	n/a
4	chr12:117595820-117595870	IMR90	lung:	fetal
5	chr12:117579332-117579382	AG04450	lung:	fetal
6	chr12:117581067-117581117	Jurkat	blood:	n/a
7	chr12:117579690-117579740	GM06990	blood:	n/a
8	chr12:117590918-117590968	AG04449	skin:	fetal
9	chr12:117590918-117590968	BJ	skin:	n/a
10	chr12:117593501-117593551	H1-hESC	embryonic stem cell:	embryo
11	chr12:117595754-117595804	GM12891	blood:	n/a
12	chr12:117595820-117595870	ProgFib	skin:	n/a
13	chr12:117581067-117581117	HCF	heart:	n/a
14	chr12:117593386-117593436	HepG2	liver:	n/a
15	chr12:117581067-117581117	NH-A	brain:	n/a
16	chr12:117595754-117595804	PFSK-1	brain:	n/a
17	chr12:117580995-117581045	HMEC	breast:	n/a
18	chr12:117579332-117579382	Hela-S3	cervix:	n/a
19	chr12:117593354-117593404	HRE	kidney:	n/a
20	chr12:117593259-117593309	HL-60	blood:	n/a
21	chr12:117583821-117583871	GM12878	blood:	n/a
22	chr12:117595738-117595788	HEK293	kidney:	embryo
23	chr12:117590918-117590968	SKMC	muscle:	n/a
24	chr12:117580007-117580057	Caco-2	colon:	n/a
25	chr12:117588951-117589001	SK-N-MC	brain:	n/a
26	chr12:117579332-117579382	HepG2	liver:	n/a
27	chr12:117562500-117562550	NHDF-neo	bronchial:	n/a
28	chr12:117593259-117593309	ovcar-3	ovarian:	n/a
29	chr12:117562500-117562550	GM12891	blood:	n/a
30	chr12:117579690-117579740	BE2_C	brain:	n/a
31	chr12:117588951-117589001	ProgFib	skin:	n/a
32	chr12:117580007-117580057	HEEpiC	esophagus:	n/a
33	chr12:117593354-117593404	T-47D	breast:	n/a
34	chr12:117593688-117593738	SKMC	muscle:	n/a
35	chr12:117593259-117593309	HEEpiC	esophagus:	n/a
36	chr12:117580007-117580057	BE2_C	brain:	n/a
37	chr12:117593688-117593738	NH-A	brain:	n/a
38	chr12:117593259-117593309	Caco-2	colon:	n/a
39	chr12:117593259-117593309	HAEpiC	amniotic membrane:	n/a
40	chr12:117580995-117581045	Caco-2	colon:	n/a
41	chr12:117590918-117590968	HL-60	blood:	n/a
42	chr12:117580007-117580057	MCF-7	breast:	n/a
43	chr12:117593688-117593738	IMR90	lung:	fetal
44	chr12:117593259-117593309	BE2_C	brain:	n/a
45	chr12:117595820-117595870	NB4	blood:	n/a
46	chr12:117593386-117593436	HAEpiC	amniotic membrane:	n/a
47	chr12:117593501-117593551	U87	brain:	n/a
48	chr12:117613954-117614004	HRPEpiC	eye:	n/a
49	chr12:117557630-117557680	HL-60	blood:	n/a
50	chr12:117593688-117593738	GM12878	blood:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:117608161..117610702-chr12:117612350..117614705,2	K562	blood:
2	chr12:117463086..117464021-chr12:117557211..117558240,9	MCF-7	breast:
3	chr12:117140690..117141624-chr12:117557280..117558280,3	K562	blood:
4	chr12:117604447..117607084-chr12:117615834..117618486,2	MCF-7	breast:
5	chr12:117575984..117579086-chr12:117579299..117582176,4	MCF-7	breast:
6	chr12:117557753..117559433-chr12:117563152..117564669,2	K562	blood:
7	chr12:117584695..117586199-chr12:117591646..117594518,2	MCF-7	breast:
8	chr12:117563617..117566277-chr12:117584320..117585955,2	MCF-7	breast:
9	chr12:117549512..117551256-chr12:117563956..117566230,2	K562	blood:
10	chr12:117580874..117582720-chr12:117585893..117588244,3	MCF-7	breast:
11	chr12:117600913..117606514-chr12:117609706..117614136,6	MCF-7	breast:
12	chr12:117578341..117580665-chr12:117585806..117587323,2	MCF-7	breast:
13	chr12:117596904..117598821-chr12:117601061..117603560,2	MCF-7	breast:
14	chr12:117592798..117593660-chr8:132748956..132749846,2	MCF-7	breast:
15	chr12:117462662..117464720-chr12:117586991..117588878,2	MCF-7	breast:
16	chr12:117581744..117585061-chr12:117588587..117590635,3	MCF-7	breast:
17	chr12:117587228..117589286-chr12:117592743..117594300,2	K562	blood:
18	chr12:117465400..117467600-chr12:117591439..117594342,2	MCF-7	breast:
19	chr12:117579571..117583522-chr12:117585472..117588878,4	K562	blood:
20	chr12:117463075..117463618-chr12:117558464..117559173,2	MCF-7	breast:
21	chr12:117551504..117553337-chr12:117553623..117555304,2	K562	blood:
22	chr12:117620005..117621839-chr12:117627991..117629764,2	MCF-7	breast:
23	chr12:117621447..117623322-chr12:117627669..117629286,2	MCF-7	breast:
24	chr12:117579571..117583522-chr12:117585472..117588878,4	K562	blood:
25	chr12:117578702..117581617-chr12:117599263..117601278,2	MCF-7	breast:
26	chr12:117557112..117559905-chr22:42664241..42667013,2	MCF-7	breast:
27	chr12:117463072..117464125-chr12:117557237..117558458,16	MCF-7	breast:
28	chr12:117608161..117610702-chr12:117612350..117614705,2	K562	blood:
29	chr12:117577294..117579486-chr12:117626844..117629841,2	MCF-7	breast:
30	chr12:117587228..117589286-chr12:117592743..117594300,2	K562	blood:
31	chr12:117618719..117620255-chr12:117621421..117622933,2	MCF-7	breast:
32	chr12:117621580..117624392-chr12:117625961..117628023,2	K562	blood:
33	chr12:117611828..117614265-chr12:117616763..117619473,3	K562	blood:
34	chr12:117604927..117606526-chr12:117627464..117630069,2	K562	blood:
35	chr12:117596904..117598821-chr12:117601061..117603560,2	MCF-7	breast:
36	chr12:117563780..117567110-chr12:117568680..117571095,3	MCF-7	breast:
37	chr12:117594472..117596198-chr12:117621574..117623321,2	K562	blood:
38	chr12:117560289..117562463-chr12:117565995..117568462,3	K562	blood:
39	chr12:117566175..117568422-chr12:117574241..117576485,2	MCF-7	breast:
40	chr12:117606727..117609238-chr12:117612177..117615270,4	MCF-7	breast:
41	chr12:117611249..117613740-chr12:117613939..117616846,3	MCF-7	breast:
42	chr12:117584695..117586199-chr12:117591646..117594518,2	MCF-7	breast:
43	chr12:117616880..117620516-chr12:117626730..117630376,5	K562	blood:
44	chr12:117581744..117585061-chr12:117588587..117590635,3	MCF-7	breast:
45	chr12:117578341..117580665-chr12:117585806..117587323,2	MCF-7	breast:
46	chr12:117610469..117613124-chr12:117617825..117619883,2	MCF-7	breast:
47	chr12:117606727..117609238-chr12:117612177..117615270,4	MCF-7	breast:
48	chr12:117560289..117562463-chr12:117565995..117568462,3	K562	blood:
49	chr12:117612768..117619869-chr12:117625654..117629590,13	MCF-7	breast:
50	chr12:117618719..117620255-chr12:117621421..117622933,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXW8-1	chr12:117579196-117579896	ENSG00000258285
2	lnc-FBXW8-1	chr12:117579196-117579789	NONHSAT030980

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	FBXO21	hsa-miR-340-5p	chr12:117581815-117581809
2	FBXO21	hsa-miR-96-5p	chr12:117581632-117581654
3	FBXO21	hsa-miR-340-5p	chr12:117581809-117581832

Variant related genes	Relation type
FBXO21	TF binding region
FBXO21	CpG island
ENSG00000174989	chromatin interactions
ENSG00000088992	chromatin interactions
ENSG00000135108	chromatin interactions
ENSG00000258285	chromatin interactions
ENSG00000182057	chromatin interactions
PHLPP2	miRNA target sites

Extended variants
information (count: 3246 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3246 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10850762	chr12:117549739-117549740	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74724753	chr12:117549750-117549751	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs149564482	chr12:117549764-117549765	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs181541512	chr12:117549783-117549784	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs77902580	chr12:117549810-117549811	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs147238513	chr12:117549836-117549837	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs571020623	chr12:117549892-117549893	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs540042886	chr12:117550002-117550003	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs184629681	chr12:117550019-117550020	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs115876181	chr12:117550020-117550021	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs188653034	chr12:117550096-117550097	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs555761315	chr12:117550100-117550101	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs575571915	chr12:117550119-117550120	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs543669150	chr12:117550182-117550183	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs563445907	chr12:117550226-117550227	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs397753586	chr12:117550235-117550236	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs576581757	chr12:117550268-117550269	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs545637794	chr12:117550290-117550291	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs559014443	chr12:117550301-117550302	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs113613572	chr12:117550465-117550466	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs531294706	chr12:117550487-117550488	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs547851472	chr12:117550491-117550492	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs561693779	chr12:117550494-117550495	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs549156275	chr12:117550521-117550522	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs181417788	chr12:117550551-117550552	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs115569296	chr12:117550562-117550563	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs571210230	chr12:117550618-117550619	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs12372620	chr12:117550635-117550636	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs116771703	chr12:117550636-117550637	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs112826540	chr12:117550641-117550642	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs140848960	chr12:117550690-117550691	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs545484667	chr12:117550693-117550694	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs569150702	chr12:117550717-117550718	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs539793120	chr12:117550731-117550732	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs10161492	chr12:117550733-117550734	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs555597008	chr12:117550748-117550749	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs61937046	chr12:117550776-117550777	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191049829	chr12:117550795-117550796	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs556833490	chr12:117550871-117550872	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs4379913	chr12:117550914-117550915	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs545578136	chr12:117550930-117550931	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs561171486	chr12:117550931-117550932	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs79146217	chr12:117550964-117550965	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs10682218	chr12:117550965-117550966	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs559147875	chr12:117550979-117550980	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs181992102	chr12:117550996-117550997	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs114506152	chr12:117551073-117551074	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs561636787	chr12:117551081-117551082	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs2893705	chr12:117551142-117551143	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs142591767	chr12:117551143-117551144	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD

Chromatin state (count:1801 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117537600-117556400	Weak transcription	Right Atrium	heart
2	chr12:117548200-117550600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:117548200-117551800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr12:117548400-117550400	Enhancers	Primary hematopoietic stem cells	blood
5	chr12:117548400-117550800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:117548800-117550000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:117549000-117550000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr12:117549200-117550000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr12:117549200-117550000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr12:117549200-117550000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:117549200-117550000	Enhancers	H9 Cell Line	embryonic stem cell
12	chr12:117549200-117550000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr12:117549200-117550000	Enhancers	Brain Germinal Matrix	brain
14	chr12:117549200-117550000	Enhancers	Pancreas	Pancrea
15	chr12:117549200-117550000	Flanking Bivalent TSS/Enh	HepG2	liver
16	chr12:117549200-117550200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr12:117549200-117550200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr12:117549200-117550200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:117549200-117550200	Enhancers	Fetal Muscle Leg	muscle
20	chr12:117549200-117550200	Bivalent Enhancer	Fetal Stomach	stomach
21	chr12:117549200-117550400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:117549200-117550400	Enhancers	Fetal Lung	lung
23	chr12:117549200-117550400	Enhancers	Thymus	Thymus
24	chr12:117549200-117550600	Enhancers	Fetal Thymus	thymus
25	chr12:117549400-117549800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:117549400-117550000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr12:117549400-117550000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr12:117549400-117550200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr12:117549400-117550200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr12:117549400-117550200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:117549400-117550200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr12:117549400-117550200	Enhancers	Fetal Brain Male	brain
33	chr12:117549400-117550200	Enhancers	K562	blood
34	chr12:117549400-117550400	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr12:117549400-117550600	Enhancers	Dnd41	blood
36	chr12:117549600-117549800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr12:117549600-117550000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr12:117549600-117550000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:117549600-117550000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:117549600-117550000	Bivalent Enhancer	Adipose Nuclei	Adipose
41	chr12:117549600-117550000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr12:117549600-117550000	Enhancers	Placenta	Placenta
43	chr12:117549600-117550000	Enhancers	Placenta Amnion	Placenta Amnion
44	chr12:117549600-117550200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
45	chr12:117549800-117550000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:117549800-117550000	Bivalent Enhancer	Fetal Intestine Large	intestine
47	chr12:117549800-117550200	Enhancers	Fetal Kidney	kidney
48	chr12:117550000-117550200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr12:117550000-117550600	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr12:117550000-117550800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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