Variant report

Variant	esv1804583
Chromosome Location	chr12:117472107-117525169
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:822)
CpG islands
(count:1831)
Chromatin interactive
region (count:47)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:822 , 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	chr12:117480142-117480490	K562	blood:	n/a	n/a
2	ARID3A	chr12:117485974-117486354	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:117496405-117496605	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:117480848-117481226	K562	blood:	n/a	n/a
5	ARID3A	chr12:117483217-117484132	HepG2	liver:	n/a	n/a
6	ATF1	chr12:117480768-117481088	K562	blood:	n/a	n/a
7	ATF3	chr12:117480160-117480451	K562	blood:	n/a	n/a
8	ATF3	chr12:117480063-117480501	K562	blood:	n/a	n/a
9	BACH1	chr12:117480144-117480444	K562	blood:	n/a	chr12:117480343-117480357
10	BACH1	chr12:117490676-117490868	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr12:117490524-117490764	GM12878	blood:	n/a	n/a
12	BCL3	chr12:117479931-117480532	K562	blood:	n/a	chr12:117480249-117480256
13	BHLHE40	chr12:117498834-117498983	K562	blood:	n/a	n/a
14	BHLHE40	chr12:117508038-117508047	K562	blood:	n/a	n/a
15	BHLHE40	chr12:117479834-117481093	K562	blood:	n/a	n/a
16	BHLHE40	chr12:117488807-117488899	K562	blood:	n/a	n/a
17	BHLHE40	chr12:117482862-117482922	K562	blood:	n/a	n/a
18	BHLHE40	chr12:117491467-117491666	K562	blood:	n/a	n/a
19	BHLHE40	chr12:117498163-117498443	K562	blood:	n/a	n/a
20	BHLHE40	chr12:117483249-117483514	K562	blood:	n/a	chr12:117483416-117483432
21	BHLHE40	chr12:117487124-117487373	K562	blood:	n/a	n/a
22	BHLHE40	chr12:117501039-117501424	GM12878	blood:	n/a	n/a
23	BRCA1	chr12:117482821-117482889	HepG2	liver:	n/a	n/a
24	BRCA1	chr12:117484045-117484078	HepG2	liver:	n/a	n/a
25	CBX3	chr12:117480090-117480450	K562	blood:	n/a	n/a
26	CBX3	chr12:117484681-117484988	K562	blood:	n/a	n/a
27	CBX3	chr12:117479967-117480589	K562	blood:	n/a	n/a
28	CCNT2	chr12:117479701-117481115	K562	blood:	n/a	chr12:117480239-117480259 chr12:117480086-117480095 chr12:117480092-117480101
29	CCNT2	chr12:117507864-117508064	K562	blood:	n/a	n/a
30	CCNT2	chr12:117486450-117486728	K562	blood:	n/a	n/a
31	CEBPB	chr12:117480039-117480531	K562	blood:	n/a	n/a
32	CEBPB	chr12:117505718-117505744	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:117480113-117480480	K562	blood:	n/a	n/a
34	CEBPB	chr12:117505683-117505787	K562	blood:	n/a	n/a
35	CEBPB	chr12:117517579-117517659	K562	blood:	n/a	n/a
36	CEBPB	chr12:117479123-117479231	K562	blood:	n/a	n/a
37	CEBPD	chr12:117482699-117483063	HepG2	liver:	n/a	n/a
38	CEBPD	chr12:117483188-117483643	HepG2	liver:	n/a	n/a
39	CEBPD	chr12:117479914-117480639	K562	blood:	n/a	n/a
40	CEBPD	chr12:117479857-117481120	K562	blood:	n/a	n/a
41	CHD2	chr12:117479635-117480768	K562	blood:	n/a	n/a
42	CHD2	chr12:117490471-117490867	GM12878	blood:	n/a	n/a
43	CHD2	chr12:117482842-117482970	K562	blood:	n/a	n/a
44	CHD2	chr12:117483166-117483557	HepG2	liver:	n/a	n/a
45	CHD2	chr12:117477355-117477423	HepG2	liver:	n/a	n/a
46	CHD2	chr12:117500870-117500985	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr12:117500985-117501464	GM12878	blood:	n/a	n/a
48	CHD2	chr12:117490409-117490815	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr12:117482770-117482948	HepG2	liver:	n/a	n/a
50	CHD2	chr12:117483892-117484069	HepG2	liver:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117484306-117484356	BE2_C	brain:	n/a
2	chr12:117484306-117484356	BE2_C	brain:	n/a
3	chr12:117477926-117477976	SAEC	small airway:	n/a
4	chr12:117477387-117477437	NT2-D1	testis:	n/a
5	chr12:117478480-117478530	H1-hESC	embryonic stem cell:	embryo
6	chr12:117486164-117486214	Hepatocyte	liver:	n/a
7	chr12:117477424-117477474	K562	blood:	n/a
8	chr12:117477837-117477887	NHDF-neo	bronchial:	n/a
9	chr12:117478480-117478530	AG10803	skin:	n/a
10	chr12:117486878-117486928	Jurkat	blood:	n/a
11	chr12:117490038-117490088	NT2-D1	testis:	n/a
12	chr12:117484926-117484976	LNCaP	prostate:	n/a
13	chr12:117484521-117484571	U87	brain:	n/a
14	chr12:117477424-117477474	ovcar-3	ovarian:	n/a
15	chr12:117477926-117477976	AoSMC	blood vessel:	n/a
16	chr12:117487037-117487087	AG10803	skin:	n/a
17	chr12:117477837-117477887	U87	brain:	n/a
18	chr12:117480333-117480383	NT2-D1	testis:	n/a
19	chr12:117484926-117484976	GM12892	blood:	n/a
20	chr12:117484306-117484356	HEEpiC	esophagus:	n/a
21	chr12:117473375-117473425	HRE	kidney:	n/a
22	chr12:117490038-117490088	Jurkat	blood:	n/a
23	chr12:117483006-117483056	HRPEpiC	eye:	n/a
24	chr12:117484521-117484571	IMR90	lung:	fetal
25	chr12:117487037-117487087	PrEC	prostate:	n/a
26	chr12:117484948-117484998	HUVEC	blood vessel:	n/a
27	chr12:117477926-117477976	HIPEpiC	eye:	n/a
28	chr12:117483310-117483360	Hepatocyte	liver:	n/a
29	chr12:117483006-117483056	ProgFib	skin:	n/a
30	chr12:117484521-117484571	BE2_C	brain:	n/a
31	chr12:117487037-117487087	NB4	blood:	n/a
32	chr12:117477105-117477155	AG09319	gingival:	n/a
33	chr12:117501447-117501497	HL-60	blood:	n/a
34	chr12:117477387-117477437	IMR90	lung:	fetal
35	chr12:117476704-117476754	ProgFib	skin:	n/a
36	chr12:117477424-117477474	HUVEC	blood vessel:	n/a
37	chr12:117477481-117477531	ovcar-3	ovarian:	n/a
38	chr12:117473375-117473425	Jurkat	blood:	n/a
39	chr12:117480333-117480383	ECC-1	luminal epithelium:	n/a
40	chr12:117476838-117476888	IMR90	lung:	fetal
41	chr12:117483310-117483360	LNCaP	prostate:	n/a
42	chr12:117477926-117477976	NB4	blood:	n/a
43	chr12:117474507-117474557	SKMC	muscle:	n/a
44	chr12:117484975-117485025	K562	blood:	n/a
45	chr12:117484948-117484998	HEK293	kidney:	embryo
46	chr12:117486164-117486214	HNPCEpiC	eye:	n/a
47	chr12:117483086-117483136	AoSMC	blood vessel:	n/a
48	chr12:117484948-117484998	SK-N-SH	brain:	n/a
49	chr12:117477000-117477050	SK-N-MC	brain:	n/a
50	chr12:117477926-117477976	A549	lung:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:117513474..117515801-chr12:117535045..117537762,2	K562	blood:
2	chr12:117473852..117475862-chr12:117477409..117479027,2	K562	blood:
3	chr12:117478574..117480262-chr12:117481796..117483489,2	K562	blood:
4	chr12:117470409..117472666-chr12:117473842..117475716,2	MCF-7	breast:
5	chr12:117397026..117399218-chr12:117481554..117483572,2	MCF-7	breast:
6	chr12:117520699..117522786-chr12:117526190..117528130,2	MCF-7	breast:
7	chr12:117486751..117489463-chr12:117503147..117505239,2	K562	blood:
8	chr12:117501229..117502760-chr12:117508705..117510581,2	K562	blood:
9	chr12:117461681..117464080-chr12:117470751..117473024,2	MCF-7	breast:
10	chr12:117498452..117500621-chr12:117503397..117505307,2	K562	blood:
11	chr12:117516404..117518439-chr12:117535649..117537690,2	MCF-7	breast:
12	chr12:117512300..117515026-chr12:117517081..117519367,2	MCF-7	breast:
13	chr12:117498452..117500621-chr12:117503397..117505307,2	K562	blood:
14	chr12:117477334..117479654-chr12:117535029..117537514,2	MCF-7	breast:
15	chr12:117517303..117519421-chr12:117527171..117531025,3	K562	blood:
16	chr12:117477087..117480724-chr12:117486826..117489814,3	MCF-7	breast:
17	chr12:117507312..117509184-chr12:117522050..117524792,2	K562	blood:
18	chr12:117468241..117470806-chr12:117471546..117474082,2	K562	blood:
19	chr12:117507312..117509184-chr12:117522050..117524792,2	K562	blood:
20	chr12:117522325..117524355-chr12:117524708..117526687,2	K562	blood:
21	chr12:117522745..117531514-chr12:117533680..117541602,11	K562	blood:
22	chr1:225965395..225967471-chr12:117490550..117492773,2	MCF-7	breast:
23	chr12:117477087..117480724-chr12:117486826..117489814,3	MCF-7	breast:
24	chr12:117474107..117476260-chr12:117479053..117480965,2	K562	blood:
25	chr12:117501550..117503831-chr12:117535985..117538295,2	MCF-7	breast:
26	chr12:117465370..117468011-chr12:117469598..117472527,2	K562	blood:
27	chr12:117469991..117472353-chr12:117476644..117478230,2	MCF-7	breast:
28	chr12:117488907..117491503-chr12:117528799..117530966,2	K562	blood:
29	chr12:117470652..117475607-chr12:117477009..117480553,6	K562	blood:
30	chr12:117470409..117472666-chr12:117473842..117475716,2	MCF-7	breast:
31	chr12:117478764..117480337-chr12:117507542..117509492,2	K562	blood:
32	chr12:117469991..117472353-chr12:117476644..117478230,2	MCF-7	breast:
33	chr12:117521637..117523408-chr12:117528244..117530881,2	MCF-7	breast:
34	chr12:117491735..117493478-chr12:117493930..117496851,2	MCF-7	breast:
35	chr12:117512300..117515026-chr12:117517081..117519367,2	MCF-7	breast:
36	chr12:117507986..117510035-chr20:49345785..49347332,2	MCF-7	breast:
37	chr12:117495577..117497098-chr12:117535967..117538055,2	K562	blood:
38	chr12:117522325..117524355-chr12:117524708..117526687,2	K562	blood:
39	chr12:117522125..117522808-chr17:25620752..25621663,2	NB4	blood:
40	chr12:117478574..117480262-chr12:117481796..117483489,2	K562	blood:
41	chr12:117501229..117502760-chr12:117508705..117510581,2	K562	blood:
42	chr12:117473852..117475862-chr12:117477409..117479027,2	K562	blood:
43	chr12:117478356..117481644-chr12:117536617..117538572,3	K562	blood:
44	chr12:117474107..117476260-chr12:117479053..117480965,2	K562	blood:
45	chr12:117486751..117489463-chr12:117503147..117505239,2	K562	blood:
46	chr12:117478764..117480337-chr12:117507542..117509492,2	K562	blood:
47	chr12:117470652..117475607-chr12:117477009..117480553,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO21-2	chr12:117513102-117513145	NONHSAT030979

No data

Variant related genes	Relation type
TESC	TF binding region
TESC	CpG island
ENSG00000088992	chromatin interactions
ENSG00000263583	chromatin interactions
ENSG00000258285	chromatin interactions
ENSG00000143742	chromatin interactions
ENSG00000109046	chromatin interactions

Extended variants
information (count: 2399 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2399 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117720927	chr12:117472122-117472123	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs561273497	chr12:117472144-117472145	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs16947246	chr12:117472151-117472152	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs550210044	chr12:117472161-117472162	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs185543537	chr12:117472163-117472164	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs190314018	chr12:117472186-117472187	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs551566503	chr12:117472221-117472222	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571401305	chr12:117472247-117472248	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555160528	chr12:117472252-117472253	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533772865	chr12:117472266-117472267	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533412651	chr12:117472268-117472269	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139482945	chr12:117472287-117472288	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138204771	chr12:117472293-117472294	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs143701976	chr12:117472303-117472304	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552167249	chr12:117472368-117472369	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530574458	chr12:117472374-117472375	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182487984	chr12:117472375-117472376	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562834133	chr12:117472408-117472409	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs545281442	chr12:117472417-117472418	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs139128570	chr12:117472425-117472426	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs531368808	chr12:117472435-117472436	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs116741024	chr12:117472454-117472455	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs572598473	chr12:117472468-117472469	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs541305510	chr12:117472480-117472481	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs200867058	chr12:117472483-117472484	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs11310785	chr12:117472488-117472489	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs398076987	chr12:117472491-117472492	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs201023873	chr12:117472493-117472494	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs147143988	chr12:117472520-117472521	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs117640035	chr12:117472544-117472545	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs140280989	chr12:117472599-117472600	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs12299197	chr12:117472617-117472618	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs532582475	chr12:117472642-117472643	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs79190773	chr12:117472645-117472646	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs533882159	chr12:117472648-117472649	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs547555267	chr12:117472662-117472663	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs571495353	chr12:117472705-117472706	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs527470665	chr12:117472730-117472731	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs558683246	chr12:117472737-117472738	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs567307542	chr12:117472756-117472757	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs535962915	chr12:117472765-117472766	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs570349329	chr12:117472775-117472776	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs555875018	chr12:117472792-117472793	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs569289045	chr12:117472793-117472794	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs12313091	chr12:117472826-117472827	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs559195003	chr12:117472830-117472831	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs186069622	chr12:117472835-117472836	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs576954922	chr12:117472889-117472890	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs189231143	chr12:117472895-117472896	Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs554890057	chr12:117472931-117472932	Weak transcription Genic enhancers Enhancers Strong transcription 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:1333 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117452800-117479000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr12:117462000-117477400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr12:117466200-117474600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr12:117466400-117473800	Weak transcription	Aorta	Aorta
5	chr12:117466400-117475600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:117466600-117479800	Weak transcription	Hela-S3	cervix
7	chr12:117467000-117475400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr12:117467000-117479600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr12:117467200-117475400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr12:117467400-117486000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr12:117468200-117477000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr12:117468600-117477400	Weak transcription	Primary B cells from cord blood	blood
13	chr12:117469200-117474800	Weak transcription	Lung	lung
14	chr12:117469800-117474600	Enhancers	Fetal Heart	heart
15	chr12:117470000-117472200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:117470200-117472200	Bivalent Enhancer	Fetal Thymus	thymus
17	chr12:117470200-117472600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr12:117470400-117472400	Strong transcription	A549	lung
19	chr12:117470400-117476800	Enhancers	Stomach Mucosa	stomach
20	chr12:117470600-117472200	Enhancers	Brain Angular Gyrus	brain
21	chr12:117470600-117472600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
22	chr12:117470600-117473000	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr12:117470800-117472400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr12:117470800-117472600	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr12:117470800-117472800	Bivalent Enhancer	Fetal Brain Male	brain
26	chr12:117470800-117472800	Enhancers	Right Ventricle	heart
27	chr12:117470800-117474600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr12:117470800-117474800	Enhancers	Left Ventricle	heart
29	chr12:117470800-117476400	Strong transcription	Dnd41	blood
30	chr12:117470800-117483400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr12:117471000-117472200	Bivalent Enhancer	Fetal Intestine Small	intestine
32	chr12:117471000-117472200	Bivalent Enhancer	Fetal Lung	lung
33	chr12:117471000-117472200	Enhancers	Right Atrium	heart
34	chr12:117471000-117472400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:117471200-117472200	Enhancers	Brain Anterior Caudate	brain
36	chr12:117471200-117472400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr12:117471200-117472400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr12:117471200-117472600	Bivalent Enhancer	Fetal Stomach	stomach
39	chr12:117471200-117482800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr12:117471400-117472200	Bivalent Enhancer	Fetal Kidney	kidney
41	chr12:117471400-117472600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr12:117471400-117472600	Enhancers	Ovary	ovary
43	chr12:117471400-117473600	Weak transcription	Thymus	Thymus
44	chr12:117471400-117479800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:117471600-117472200	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
46	chr12:117471600-117472200	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
47	chr12:117471600-117472400	Weak transcription	Gastric	stomach
48	chr12:117471600-117472600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
49	chr12:117471600-117473200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr12:117471600-117474200	Strong transcription	HepG2	liver

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