Variant report

Variant	nsv519118
Chromosome Location	chr12:117386085-117521180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1925)
CpG islands
(count:3969)
Chromatin interactive
region (count:124)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1925 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:117480848-117481226	K562	blood:	n/a	n/a
2	ARID3A	chr12:117483217-117484132	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:117496405-117496605	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:117485974-117486354	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:117480142-117480490	K562	blood:	n/a	n/a
6	ARID3A	chr12:117463407-117463608	HepG2	liver:	n/a	n/a
7	ATF1	chr12:117417942-117418220	K562	blood:	n/a	n/a
8	ATF1	chr12:117443229-117443727	K562	blood:	n/a	n/a
9	ATF1	chr12:117393420-117393792	K562	blood:	n/a	n/a
10	ATF1	chr12:117480768-117481088	K562	blood:	n/a	n/a
11	ATF1	chr12:117388622-117388796	K562	blood:	n/a	n/a
12	ATF2	chr12:117463325-117463724	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr12:117393446-117393835	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr12:117480063-117480501	K562	blood:	n/a	n/a
15	ATF3	chr12:117463242-117463931	A549	lung:	n/a	chr12:117463449-117463458
16	ATF3	chr12:117480160-117480451	K562	blood:	n/a	n/a
17	ATF3	chr12:117463692-117463900	K562	blood:	n/a	n/a
18	ATF3	chr12:117393382-117393796	K562	blood:	n/a	n/a
19	ATF3	chr12:117463348-117463642	K562	blood:	n/a	chr12:117463449-117463458
20	ATF3	chr12:117443350-117443526	K562	blood:	n/a	n/a
21	BACH1	chr12:117438262-117438324	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr12:117458686-117458904	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr12:117443378-117443527	K562	blood:	n/a	n/a
24	BACH1	chr12:117480144-117480444	K562	blood:	n/a	chr12:117480343-117480357
25	BACH1	chr12:117490676-117490868	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr12:117463352-117463607	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr12:117469430-117469618	GM12878	blood:	n/a	n/a
28	BATF	chr12:117397937-117398260	GM12878	blood:	n/a	chr12:117398144-117398155
29	BATF	chr12:117397894-117398318	GM12878	blood:	n/a	chr12:117398144-117398155
30	BCL11A	chr12:117397999-117398239	GM12878	blood:	n/a	chr12:117398184-117398193
31	BCL11A	chr12:117490524-117490764	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:117397904-117398271	GM12878	blood:	n/a	chr12:117398184-117398193 chr12:117398234-117398243
33	BCL3	chr12:117457701-117457963	GM12878	blood:	n/a	n/a
34	BCL3	chr12:117479931-117480532	K562	blood:	n/a	chr12:117480249-117480256
35	BCL3	chr12:117434525-117434777	GM12878	blood:	n/a	n/a
36	BCL3	chr12:117463187-117463766	A549	lung:	n/a	n/a
37	BCL3	chr12:117448059-117448309	GM12878	blood:	n/a	chr12:117448110-117448119
38	BCLAF1	chr12:117397857-117398362	GM12878	blood:	n/a	chr12:117398184-117398193 chr12:117398234-117398243
39	BHLHE40	chr12:117487124-117487373	K562	blood:	n/a	n/a
40	BHLHE40	chr12:117498163-117498443	K562	blood:	n/a	n/a
41	BHLHE40	chr12:117479834-117481093	K562	blood:	n/a	n/a
42	BHLHE40	chr12:117443236-117443823	K562	blood:	n/a	n/a
43	BHLHE40	chr12:117491467-117491666	K562	blood:	n/a	n/a
44	BHLHE40	chr12:117501039-117501424	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:117508038-117508047	K562	blood:	n/a	n/a
46	BHLHE40	chr12:117482862-117482922	K562	blood:	n/a	n/a
47	BHLHE40	chr12:117463293-117463915	K562	blood:	n/a	n/a
48	BHLHE40	chr12:117498834-117498983	K562	blood:	n/a	n/a
49	BHLHE40	chr12:117488807-117488899	K562	blood:	n/a	n/a
50	BHLHE40	chr12:117463451-117463697	GM12878	blood:	n/a	n/a

(count:3969 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117457813-117457863	HCF	heart:	n/a
2	chr12:117470568-117470618	HNPCEpiC	eye:	n/a
3	chr12:117473375-117473425	LNCaP	prostate:	n/a
4	chr12:117425053-117425103	MCF10A-Er-Src	breast:	n/a
5	chr12:117457813-117457863	HCF	heart:	n/a
6	chr12:117470568-117470618	HNPCEpiC	eye:	n/a
7	chr12:117473375-117473425	LNCaP	prostate:	n/a
8	chr12:117425053-117425103	MCF10A-Er-Src	breast:	n/a
9	chr12:117468289-117468339	AG09319	gingival:	n/a
10	chr12:117468061-117468111	ECC-1	luminal epithelium:	n/a
11	chr12:117470541-117470591	HEEpiC	esophagus:	n/a
12	chr12:117457813-117457863	SK-N-MC	brain:	n/a
13	chr12:117471700-117471750	MCF-7	breast:	n/a
14	chr12:117476704-117476754	NH-A	brain:	n/a
15	chr12:117408163-117408213	PrEC	prostate:	n/a
16	chr12:117483310-117483360	HRCEpiC	kidney:	n/a
17	chr12:117483006-117483056	CMK	blood:	n/a
18	chr12:117470568-117470618	Caco-2	colon:	n/a
19	chr12:117486164-117486214	PrEC	prostate:	n/a
20	chr12:117477105-117477155	AG04449	skin:	fetal
21	chr12:117457813-117457863	NHDF-neo	bronchial:	n/a
22	chr12:117401813-117401863	HMEC	breast:	n/a
23	chr12:117468529-117468579	NHDF-neo	bronchial:	n/a
24	chr12:117468061-117468111	H1-hESC	embryonic stem cell:	embryo
25	chr12:117465849-117465899	K562	blood:	n/a
26	chr12:117408122-117408172	SAEC	small airway:	n/a
27	chr12:117407970-117408020	AG09309	skin:	n/a
28	chr12:117470568-117470618	GM19239	blood:	n/a
29	chr12:117487037-117487087	ECC-1	luminal epithelium:	n/a
30	chr12:117468529-117468579	NB4	blood:	n/a
31	chr12:117457846-117457896	SK-N-MC	brain:	n/a
32	chr12:117477000-117477050	HCF	heart:	n/a
33	chr12:117470549-117470599	PANC-1	pancreas:	n/a
34	chr12:117477105-117477155	HPAEpiC	pulmonary alveolar:	n/a
35	chr12:117425245-117425295	T-47D	breast:	n/a
36	chr12:117407879-117407929	GM06990	blood:	n/a
37	chr12:117448211-117448261	AG04449	skin:	fetal
38	chr12:117415439-117415489	HepG2	liver:	n/a
39	chr12:117477387-117477437	CMK	blood:	n/a
40	chr12:117476838-117476888	RPTEC	kidney:	n/a
41	chr12:117486878-117486928	RPTEC	kidney:	n/a
42	chr12:117484521-117484571	BJ	skin:	n/a
43	chr12:117470875-117470925	HNPCEpiC	eye:	n/a
44	chr12:117471086-117471136	HEK293	kidney:	embryo
45	chr12:117478480-117478530	MCF10A-Er-Src	breast:	n/a
46	chr12:117401813-117401863	ovcar-3	ovarian:	n/a
47	chr12:117440120-117440170	SKMC	muscle:	n/a
48	chr12:117486878-117486928	NT2-D1	testis:	n/a
49	chr12:117470568-117470618	NHDF-neo	bronchial:	n/a
50	chr12:117483310-117483360	PANC-1	pancreas:	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:225965395..225967471-chr12:117490550..117492773,2	MCF-7	breast:
2	chr12:117437746..117440229-chr12:117441303..117443639,2	K562	blood:
3	chr12:117469991..117472353-chr12:117476644..117478230,2	MCF-7	breast:
4	chr12:117486751..117489463-chr12:117503147..117505239,2	K562	blood:
5	chr12:117409582..117412431-chr12:117414257..117415870,2	MCF-7	breast:
6	chr12:117455374..117458365-chr12:117461422..117463402,2	MCF-7	breast:
7	chr12:117507312..117509184-chr12:117522050..117524792,2	K562	blood:
8	chr12:117401492..117403135-chr12:117411916..117413854,2	K562	blood:
9	chr12:117349929..117351804-chr12:117393764..117395801,2	MCF-7	breast:
10	chr12:117463061..117463973-chr12:117592706..117593552,4	K562	blood:
11	chr12:117462978..117464343-chr12:117556869..117558882,20	K562	blood:
12	chr12:117520699..117522786-chr12:117526190..117528130,2	MCF-7	breast:
13	chr12:117478764..117480337-chr12:117507542..117509492,2	K562	blood:
14	chr12:117140689..117141224-chr12:117393532..117394138,2	K562	blood:
15	chr12:117463086..117464021-chr12:117557211..117558240,9	MCF-7	breast:
16	chr12:117477087..117480724-chr12:117486826..117489814,3	MCF-7	breast:
17	chr12:117455374..117458365-chr12:117461422..117463402,2	MCF-7	breast:
18	chr12:117413641..117415304-chr12:117416885..117418716,2	K562	blood:
19	chr12:117447389..117449402-chr12:117456865..117458856,2	MCF-7	breast:
20	chr12:117401492..117403135-chr12:117411916..117413854,2	K562	blood:
21	chr12:117465400..117467600-chr12:117591439..117594342,2	MCF-7	breast:
22	chr12:117441591..117444664-chr12:117447106..117450120,5	MCF-7	breast:
23	chr12:117470409..117472666-chr12:117473842..117475716,2	MCF-7	breast:
24	chr12:117416955..117418879-chr12:117430472..117432333,2	K562	blood:
25	chr12:117406724..117409328-chr12:117437750..117440226,2	MCF-7	breast:
26	chr12:117405576..117408007-chr12:117626916..117629267,2	MCF-7	breast:
27	chr12:117406724..117409328-chr12:117437750..117440226,2	MCF-7	breast:
28	chr12:117424054..117426745-chr12:117430419..117432547,2	MCF-7	breast:
29	chr12:117394664..117397390-chr12:117400472..117403185,2	K562	blood:
30	chr12:117461681..117464080-chr12:117470751..117473024,2	MCF-7	breast:
31	chr12:117141137..117141688-chr12:117462896..117463565,2	K562	blood:
32	chr12:117469991..117472353-chr12:117476644..117478230,2	MCF-7	breast:
33	chr12:117394664..117397390-chr12:117400472..117403185,2	K562	blood:
34	chr12:117474107..117476260-chr12:117479053..117480965,2	K562	blood:
35	chr12:117463032..117464059-chr12:117588578..117590000,12	K562	blood:
36	chr12:117438803..117441545-chr12:117447187..117449859,2	K562	blood:
37	chr12:117454524..117457416-chr12:117594664..117596732,2	K562	blood:
38	chr12:117383644..117386038-chr12:117390452..117392333,2	K562	blood:
39	chr12:117498452..117500621-chr12:117503397..117505307,2	K562	blood:
40	chr12:117447389..117449402-chr12:117456865..117458856,2	MCF-7	breast:
41	chr12:117421809..117423733-chr12:117438090..117440215,2	MCF-7	breast:
42	chr12:117477087..117480724-chr12:117486826..117489814,3	MCF-7	breast:
43	chr12:117384024..117385524-chr12:117385938..117388865,2	K562	blood:
44	chr12:117371490..117373713-chr12:117436920..117439603,2	K562	blood:
45	chr12:117461681..117464080-chr12:117470751..117473024,2	MCF-7	breast:
46	chr12:117447732..117449605-chr12:117449689..117452738,3	K562	blood:
47	chr12:117507986..117510035-chr20:49345785..49347332,2	MCF-7	breast:
48	chr12:117427238..117428899-chr12:117435662..117438288,2	MCF-7	breast:
49	chr12:117478574..117480262-chr12:117481796..117483489,2	K562	blood:
50	chr12:117413641..117415304-chr12:117416885..117418716,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TESC-3	chr12:117468955-117470651	NONHSAT030978
2	lnc-TESC-4	chr12:117468114-117468161	NONHSAT030977
3	lnc-TESC-4	chr12:117468512-117468878	NONHSAT030977
4	lnc-FBXO21-2	chr12:117513102-117513145	NONHSAT030979

No data

Variant related genes	Relation type
TESC	TF binding region
ENSG00000257279	TF binding region
FBXW8	TF binding region
TESC	CpG island
ENSG00000257279	CpG island
FBXW8	CpG island
ENSG00000135108	chromatin interactions
ENSG00000143742	chromatin interactions
ENSG00000174989	chromatin interactions
ENSG00000258285	chromatin interactions
ENSG00000088992	chromatin interactions
ENSG00000257279	chromatin interactions

Extended variants
information (count: 5528 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5528 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4130296	chr12:117386085-117386086	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555216212	chr12:117386144-117386145	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73397424	chr12:117386170-117386171	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs370652093	chr12:117386175-117386176	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543902157	chr12:117386182-117386183	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187718010	chr12:117386188-117386189	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563233830	chr12:117386210-117386211	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372248535	chr12:117386234-117386235	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559300855	chr12:117386318-117386319	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563679790	chr12:117386351-117386352	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs193232687	chr12:117386388-117386389	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185742846	chr12:117386414-117386415	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545828037	chr12:117386485-117386486	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564818891	chr12:117386503-117386504	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116799084	chr12:117386524-117386525	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547157359	chr12:117386572-117386573	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376563559	chr12:117386581-117386582	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560760377	chr12:117386599-117386600	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529892615	chr12:117386712-117386713	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146950310	chr12:117386926-117386927	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569681866	chr12:117386999-117387000	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538604519	chr12:117387031-117387032	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188622942	chr12:117387064-117387065	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566342196	chr12:117387101-117387102	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535346019	chr12:117387112-117387113	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11068258	chr12:117387141-117387142	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574974629	chr12:117387143-117387144	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537287804	chr12:117387217-117387218	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557411603	chr12:117387263-117387264	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577298408	chr12:117387282-117387283	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79542857	chr12:117387325-117387326	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559069589	chr12:117387365-117387366	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370466421	chr12:117387374-117387375	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373550067	chr12:117387375-117387376	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372725345	chr12:117387383-117387384	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559339878	chr12:117387388-117387389	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74977947	chr12:117387419-117387420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575752045	chr12:117387427-117387428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145405264	chr12:117387462-117387463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs36021180	chr12:117387465-117387466	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs145823135	chr12:117387492-117387493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61748074	chr12:117387493-117387494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368238777	chr12:117387507-117387508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371809248	chr12:117387511-117387512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192129939	chr12:117387524-117387525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376186920	chr12:117387546-117387547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17583110	chr12:117387570-117387571	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs7136629	chr12:117387645-117387646	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs183809803	chr12:117387647-117387648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552160533	chr12:117387658-117387659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4372 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117358400-117392600	Weak transcription	Small Intestine	intestine
2	chr12:117363200-117399400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr12:117365000-117406000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr12:117366600-117388400	Weak transcription	K562	blood
5	chr12:117373800-117393200	Weak transcription	Stomach Mucosa	stomach
6	chr12:117378000-117392600	Weak transcription	Psoas Muscle	Psoas
7	chr12:117381200-117390200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr12:117381200-117391200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr12:117381400-117387800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:117381400-117389600	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr12:117381600-117386200	Strong transcription	Duodenum Mucosa	Duodenum
12	chr12:117381600-117387200	Weak transcription	Fetal Brain Female	brain
13	chr12:117381600-117388000	Strong transcription	Fetal Intestine Large	intestine
14	chr12:117381600-117388600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr12:117381600-117390200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr12:117381600-117390400	Strong transcription	Primary T cells from cord blood	blood
17	chr12:117381600-117390800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:117381800-117386200	Strong transcription	A549	lung
19	chr12:117381800-117387200	Weak transcription	HMEC	breast
20	chr12:117381800-117387800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:117381800-117387800	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:117381800-117389200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr12:117381800-117390000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr12:117381800-117390200	Strong transcription	Primary B cells from peripheral blood	blood
25	chr12:117381800-117390400	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr12:117381800-117391400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:117381800-117396200	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr12:117382000-117387600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr12:117382000-117388000	Strong transcription	Osteobl	bone
30	chr12:117382000-117388400	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr12:117382000-117388600	Strong transcription	Primary hematopoietic stem cells	blood
32	chr12:117382000-117391400	Strong transcription	Fetal Stomach	stomach
33	chr12:117382000-117396400	Weak transcription	GM12878-XiMat	blood
34	chr12:117382200-117387800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr12:117382400-117387800	Strong transcription	Fetal Intestine Small	intestine
36	chr12:117382400-117389400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:117382400-117390400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr12:117382400-117390600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:117382600-117408000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr12:117382800-117386200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
41	chr12:117382800-117390200	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr12:117383000-117387800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr12:117383000-117387800	Strong transcription	Fetal Muscle Leg	muscle
44	chr12:117383000-117388200	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr12:117383000-117389800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr12:117383000-117390200	Strong transcription	Adipose Nuclei	Adipose
47	chr12:117383000-117391000	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr12:117383000-117391200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr12:117383000-117391400	Strong transcription	Fetal Muscle Trunk	muscle
50	chr12:117383200-117386200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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