Variant report

Variant	nsv871182
Chromosome Location	chr1:79614989-79822735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1269)
CpG islands
(count:367)
Chromatin interactive
region (count:14)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1269 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:79728345-79728782	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:79658867-79659458	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:79658878-79659483	H1-hESC	embryonic stem cell:	n/a	chr1:79659052-79659066
4	BATF	chr1:79658879-79659230	GM12878	blood:	n/a	chr1:79659055-79659066
5	BATF	chr1:79658862-79659246	GM12878	blood:	n/a	chr1:79659055-79659066
6	BCL11A	chr1:79728386-79728591	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr1:79659126-79659356	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr1:79655568-79655570	GM12878	blood:	n/a	n/a
9	BRCA1	chr1:79617796-79617801	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr1:79658842-79659475	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:79788939-79789305	MCF-7	breast:	n/a	chr1:79789162-79789173
12	CEBPB	chr1:79718317-79718668	IMR90	lung:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
13	CEBPB	chr1:79788610-79789531	Hela-S3	cervix:	n/a	chr1:79789162-79789173
14	CEBPB	chr1:79658909-79659649	HCT-116	colon:	n/a	n/a
15	CEBPB	chr1:79788928-79789378	A549	lung:	n/a	chr1:79789162-79789173
16	CEBPB	chr1:79664513-79664900	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:79818713-79819070	A549	lung:	n/a	n/a
18	CEBPB	chr1:79788903-79789381	HCT-116	colon:	n/a	chr1:79789162-79789173
19	CEBPB	chr1:79788875-79789455	ECC-1	luminal epithelium:	n/a	chr1:79789162-79789173
20	CEBPB	chr1:79658949-79659505	HCT-116	colon:	n/a	n/a
21	CEBPB	chr1:79697141-79697455	IMR90	lung:	n/a	chr1:79697291-79697302
22	CEBPB	chr1:79738573-79738640	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:79698273-79698970	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:79712587-79712840	K562	blood:	n/a	n/a
25	CEBPB	chr1:79761760-79762117	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr1:79712529-79712866	IMR90	lung:	n/a	chr1:79712561-79712573
27	CEBPB	chr1:79718345-79718580	ECC-1	luminal epithelium:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
28	CEBPB	chr1:79818714-79819083	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:79659067-79659488	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:79788783-79789533	HCT-116	colon:	n/a	chr1:79789162-79789173
31	CEBPB	chr1:79820840-79821140	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:79659159-79659562	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:79718247-79718614	A549	lung:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
34	CEBPB	chr1:79788813-79789496	A549	lung:	n/a	chr1:79789162-79789173
35	CEBPB	chr1:79718310-79718670	Hela-S3	cervix:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
36	CEBPB	chr1:79697149-79697373	HepG2	liver:	n/a	chr1:79697291-79697302
37	CEBPB	chr1:79788426-79789597	IMR90	lung:	n/a	chr1:79789162-79789173
38	CEBPB	chr1:79654455-79654634	A549	lung:	n/a	n/a
39	CEBPB	chr1:79761760-79762116	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:79818740-79819166	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:79658668-79659683	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:79809139-79809258	A549	lung:	n/a	n/a
43	CEBPB	chr1:79761748-79762138	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:79753663-79753876	IMR90	lung:	n/a	chr1:79753717-79753728
45	CEBPB	chr1:79718318-79718634	A549	lung:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
46	CEBPB	chr1:79718304-79718629	ECC-1	luminal epithelium:	n/a	chr1:79718477-79718494 chr1:79718480-79718493
47	CEBPB	chr1:79670718-79671120	Hela-S3	cervix:	n/a	chr1:79670933-79670944
48	CEBPB	chr1:79803948-79804495	IMR90	lung:	n/a	chr1:79804061-79804074 chr1:79804061-79804072 chr1:79804061-79804074 chr1:79804411-79804424 chr1:79804062-79804073 chr1:79804061-79804074
49	CEBPB	chr1:79664528-79664874	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:79761810-79762112	ECC-1	luminal epithelium:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79726633-79726683	NHDF-neo	bronchial:	n/a
2	chr1:79726633-79726683	NHDF-neo	bronchial:	n/a
3	chr1:79658903-79658953	Caco-2	colon:	n/a
4	chr1:79726633-79726683	PrEC	prostate:	n/a
5	chr1:79658903-79658953	ECC-1	luminal epithelium:	n/a
6	chr1:79653656-79653706	HEEpiC	esophagus:	n/a
7	chr1:79658903-79658953	HIPEpiC	eye:	n/a
8	chr1:79658903-79658953	LNCaP	prostate:	n/a
9	chr1:79801791-79801841	BE2_C	brain:	n/a
10	chr1:79728608-79728658	AG10803	skin:	n/a
11	chr1:79653656-79653706	AG09309	skin:	n/a
12	chr1:79658903-79658953	H1-hESC	embryonic stem cell:	embryo
13	chr1:79726633-79726683	HEEpiC	esophagus:	n/a
14	chr1:79728608-79728658	HMEC	breast:	n/a
15	chr1:79653656-79653706	HMEC	breast:	n/a
16	chr1:79653656-79653706	HAEpiC	amniotic membrane:	n/a
17	chr1:79653656-79653706	T-47D	breast:	n/a
18	chr1:79801791-79801841	AG09319	gingival:	n/a
19	chr1:79728608-79728658	HAEpiC	amniotic membrane:	n/a
20	chr1:79726633-79726683	MCF-7	breast:	n/a
21	chr1:79653656-79653706	MCF-7	breast:	n/a
22	chr1:79728608-79728658	ECC-1	luminal epithelium:	n/a
23	chr1:79653656-79653706	Hela-S3	cervix:	n/a
24	chr1:79726633-79726683	ovcar-3	ovarian:	n/a
25	chr1:79653656-79653706	HCPEpiC	choroid plexus:	n/a
26	chr1:79627622-79627672	NH-A	brain:	n/a
27	chr1:79726633-79726683	PANC-1	pancreas:	n/a
28	chr1:79801791-79801841	ovcar-3	ovarian:	n/a
29	chr1:79658903-79658953	HCPEpiC	choroid plexus:	n/a
30	chr1:79728608-79728658	BE2_C	brain:	n/a
31	chr1:79627622-79627672	HepG2	liver:	n/a
32	chr1:79627622-79627672	AG10803	skin:	n/a
33	chr1:79627622-79627672	HUVEC	blood vessel:	n/a
34	chr1:79728608-79728658	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:79653656-79653706	Jurkat	blood:	n/a
36	chr1:79627622-79627672	MCF10A-Er-Src	breast:	n/a
37	chr1:79728608-79728658	NT2-D1	testis:	n/a
38	chr1:79728608-79728658	NB4	blood:	n/a
39	chr1:79801791-79801841	AG10803	skin:	n/a
40	chr1:79658903-79658953	PrEC	prostate:	n/a
41	chr1:79726633-79726683	ECC-1	luminal epithelium:	n/a
42	chr1:79653656-79653706	SK-N-SH_RA	brain:	n/a
43	chr1:79728608-79728658	MCF10A-Er-Src	breast:	n/a
44	chr1:79726633-79726683	HMEC	breast:	n/a
45	chr1:79801791-79801841	A549	lung:	n/a
46	chr1:79627622-79627672	IMR90	lung:	fetal
47	chr1:79627622-79627672	GM06990	blood:	n/a
48	chr1:79653656-79653706	SK-N-MC	brain:	n/a
49	chr1:79627622-79627672	PANC-1	pancreas:	n/a
50	chr1:79801791-79801841	GM12878	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:79744482..79747181-chr12:54772744..54775487,2	MCF-7	breast:
2	chr1:79616451..79619205-chr1:79639296..79641396,2	MCF-7	breast:
3	chr1:79154179..79155005-chr1:79663219..79663974,2	MCF-7	breast:
4	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
5	chr1:79725343..79726033-chr1:79818640..79819391,2	MCF-7	breast:
6	chr1:79812849..79814988-chr1:79816549..79819262,2	MCF-7	breast:
7	chr1:79725343..79726033-chr1:79818640..79819391,2	MCF-7	breast:
8	chr1:79304951..79305958-chr1:79662942..79663752,3	MCF-7	breast:
9	chr1:79728080..79730865-chr1:79731789..79734341,2	K562	blood:
10	chr1:79717844..79719500-chr13:74206627..74209123,2	MCF-7	breast:
11	chr1:79616451..79619205-chr1:79639296..79641396,2	MCF-7	breast:
12	chr1:79728080..79730865-chr1:79731789..79734341,2	K562	blood:
13	chr1:79810637..79813588-chr1:79825621..79828347,3	MCF-7	breast:
14	chr1:79702123..79704938-chr10:125479865..125482682,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFI44-1	chr1:79789454-79789644	ENSG00000235011.2
2	lnc-ELTD1-5	chr1:79789342-79789745	XLOC_000881
3	lnc-IFI44-1	chr1:79790270-79790552	NONHSAT004094
4	lnc-ELTD1-5	chr1:79789429-79789745	NONHSAT004093
5	lnc-ELTD1-5	chr1:79790271-79790552	XLOC_000881
6	lnc-ELTD1-5	chr1:79790271-79790416	NONHSAT004093
7	lnc-IFI44-2	chr1:79775231-79775346	XLOC_000266
8	lnc-IFI44-2	chr1:79775371-79775405	XLOC_000266
9	lnc-ELTD1-4	chr1:79786813-79786877	XLOC_000880
10	lnc-IFI44-1	chr1:79790385-79790548	ENSG00000235011.2
11	lnc-IFI44-1	chr1:79789341-79789745	NONHSAT004094
12	lnc-ELTD1-5	chr1:79788603-79788631	NONHSAT004093
13	lnc-ELTD1-4	chr1:79787090-79787278	XLOC_000880
14	lnc-ELTD1-3	chr1:79778966-79779074	XLOC_000879
15	lnc-ELTD1-3	chr1:79775130-79775346	XLOC_000879
16	lnc-IFI44-1	chr1:79789454-79789644	XLOC_000267
17	lnc-IFI44-1	chr1:79790384-79790534	XLOC_000267
18	lnc-IFI44-2	chr1:79735992-79736371	XLOC_000266
19	lnc-IFI44-2	chr1:79735991-79736371	NONHSAT004088
20	lnc-IFI44-2	chr1:79775230-79775405	NONHSAT004088
21	lnc-IFI44-2	chr1:79736086-79736371	XLOC_000266
22	lnc-IFI44-2	chr1:79775231-79775405	XLOC_000266

No data

Variant related genes	Relation type
ENSG00000235011	TF binding region
ENSG00000235011	CpG island
ENSG00000161642	chromatin interactions
C9orf5	miRNA target sites
BCL11A	miRNA target sites
DYRK2	miRNA target sites
ZNF652	miRNA target sites

Extended variants
information (count: 5035 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5035 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1555385	chr1:79614989-79614990	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545060982	chr1:79615004-79615005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375851325	chr1:79615010-79615011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563342660	chr1:79615039-79615040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530727136	chr1:79615040-79615041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530350166	chr1:79615049-79615050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549047250	chr1:79615062-79615063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189206608	chr1:79615095-79615096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528118055	chr1:79615099-79615100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78950258	chr1:79615108-79615109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192493547	chr1:79615115-79615116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76841948	chr1:79615123-79615124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550603260	chr1:79615126-79615127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570195784	chr1:79615159-79615160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150370481	chr1:79615164-79615165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555815037	chr1:79615185-79615186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184139313	chr1:79615219-79615220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534955387	chr1:79615255-79615256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552961585	chr1:79615263-79615264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577570980	chr1:79615285-79615286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7416482	chr1:79615288-79615289	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs189617946	chr1:79615300-79615301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369284298	chr1:79615321-79615322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145126933	chr1:79615372-79615373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560891135	chr1:79615432-79615433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576502861	chr1:79615458-79615459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142288746	chr1:79615462-79615463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181259325	chr1:79615466-79615467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs228461	chr1:79615517-79615518	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs186674169	chr1:79615519-79615520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550438956	chr1:79615528-79615529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs386632710	chr1:79615545-79615546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs228460	chr1:79615549-79615550	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549572749	chr1:79615550-79615551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs55729951	chr1:79615555-79615556	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs534992173	chr1:79615592-79615593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561448122	chr1:79615613-79615614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145736831	chr1:79615718-79615719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76590233	chr1:79615721-79615722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539005772	chr1:79615728-79615729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12046167	chr1:79615756-79615757	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs575711589	chr1:79615768-79615769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs71590793	chr1:79615778-79615779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542720353	chr1:79615813-79615814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554813005	chr1:79615823-79615824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs228459	chr1:79615848-79615849	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs138661253	chr1:79615853-79615854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189929683	chr1:79615967-79615968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142728997	chr1:79615985-79615986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1386591	chr1:79615992-79615993	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79614400-79615600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr1:79614600-79615400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:79615200-79615800	Enhancers	Fetal Stomach	stomach
4	chr1:79615600-79616200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr1:79615800-79616800	Weak transcription	Fetal Stomach	stomach
6	chr1:79616000-79617000	Enhancers	Fetal Lung	lung
7	chr1:79616200-79617200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr1:79616400-79617600	Enhancers	HUVEC	blood vessel
9	chr1:79616600-79617000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:79616800-79617600	Enhancers	Fetal Stomach	stomach
11	chr1:79617000-79618800	Weak transcription	Fetal Lung	lung
12	chr1:79617400-79617600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr1:79618800-79619800	Enhancers	Fetal Lung	lung
14	chr1:79619600-79619800	Enhancers	Adipose Nuclei	Adipose
15	chr1:79619600-79619800	Enhancers	Gastric	stomach
16	chr1:79619600-79619800	Enhancers	Left Ventricle	heart
17	chr1:79621200-79621800	Enhancers	Fetal Heart	heart
18	chr1:79621400-79621800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr1:79621600-79622000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr1:79621800-79626800	Weak transcription	Fetal Heart	heart
21	chr1:79626200-79627200	Enhancers	NH-A	brain
22	chr1:79626200-79627400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:79626200-79627600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr1:79626200-79627600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr1:79626200-79627800	Enhancers	Hela-S3	cervix
26	chr1:79626200-79627800	Enhancers	HUVEC	blood vessel
27	chr1:79626600-79627200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:79626600-79627200	Enhancers	NHDF-Ad	bronchial
29	chr1:79626600-79627200	Enhancers	Osteobl	bone
30	chr1:79626600-79627400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:79626800-79627600	Enhancers	Fetal Heart	heart
32	chr1:79626800-79627800	Enhancers	NHLF	lung
33	chr1:79631200-79631400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:79643000-79643400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:79643000-79643400	Active TSS	Adipose Nuclei	Adipose
36	chr1:79643000-79643400	Active TSS	Right Atrium	heart
37	chr1:79649600-79654000	Active TSS	Adipose Nuclei	Adipose
38	chr1:79652400-79655600	Enhancers	Hela-S3	cervix
39	chr1:79652600-79653400	Enhancers	Muscle Satellite Cultured Cells	--
40	chr1:79653000-79653200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:79653200-79653400	Enhancers	HUVEC	blood vessel
42	chr1:79653200-79653600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr1:79653200-79653800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr1:79653200-79653800	Active TSS	Fetal Muscle Leg	muscle
45	chr1:79653400-79654000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
46	chr1:79653400-79654200	Flanking Active TSS	HUVEC	blood vessel
47	chr1:79653400-79654400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:79653600-79654200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr1:79653600-79655600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:79653800-79654600	Enhancers	NH-A	brain

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