Variant report

Variant	nsv5860
Chromosome Location	chr7:97995939-98028100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:98015682-98015874	GM12878	blood:	n/a	n/a
2	BATF	chr7:98015317-98015518	GM12878	blood:	n/a	n/a
3	BCL3	chr7:98005551-98005915	GM12878	blood:	n/a	n/a
4	BHLHE40	chr7:98028084-98028406	K562	blood:	n/a	n/a
5	CBX3	chr7:98000360-98000865	HCT-116	colon:	n/a	chr7:98000809-98000820
6	CEBPB	chr7:98014722-98014852	A549	lung:	n/a	chr7:98014788-98014799
7	CEBPB	chr7:98000429-98001275	K562	blood:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
8	CEBPB	chr7:98023732-98023988	IMR90	lung:	n/a	n/a
9	CEBPB	chr7:98000475-98000745	K562	blood:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000644-98000655
10	CEBPB	chr7:98023720-98024173	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr7:98027767-98028559	A549	lung:	n/a	chr7:98027954-98027971 chr7:98027956-98027967
12	CEBPB	chr7:98000455-98001075	IMR90	lung:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
13	CEBPB	chr7:98021670-98021907	HepG2	liver:	n/a	chr7:98021755-98021766
14	CEBPB	chr7:98000455-98000970	A549	lung:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
15	CEBPB	chr7:98000506-98000872	ECC-1	luminal epithelium:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000644-98000655
16	CEBPB	chr7:98001054-98001233	K562	blood:	n/a	n/a
17	CEBPB	chr7:98000461-98001274	A549	lung:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
18	CEBPB	chr7:98000432-98000903	ECC-1	luminal epithelium:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000644-98000655
19	CEBPB	chr7:97999592-97999681	A549	lung:	n/a	n/a
20	CEBPB	chr7:98000326-98001072	HCT-116	colon:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
21	CEBPB	chr7:98000319-98001191	A549	lung:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
22	CEBPB	chr7:98000445-98000920	MCF-7	breast:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000644-98000655
23	CEBPB	chr7:98000465-98001292	K562	blood:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
24	CEBPB	chr7:98000251-98001302	Hela-S3	cervix:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
25	CEBPB	chr7:98027923-98028315	K562	blood:	n/a	chr7:98027954-98027971 chr7:98027956-98027967
26	CEBPB	chr7:97999604-97999680	K562	blood:	n/a	n/a
27	CEBPB	chr7:98000225-98000954	MCF-7	breast:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
28	CEBPB	chr7:98000466-98001023	HepG2	liver:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
29	CEBPB	chr7:98000506-98001245	H1-hESC	embryonic stem cell:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
30	CEBPB	chr7:98000310-98001196	HCT-116	colon:	n/a	chr7:98000642-98000655 chr7:98000642-98000653 chr7:98000644-98000653 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000910-98000923 chr7:98000644-98000655
31	CEBPB	chr7:98014693-98014841	K562	blood:	n/a	chr7:98014788-98014799
32	CEBPB	chr7:98014736-98014874	HepG2	liver:	n/a	chr7:98014788-98014799
33	CEBPB	chr7:98023581-98024151	A549	lung:	n/a	n/a
34	CEBPB	chr7:98027886-98028086	HepG2	liver:	n/a	chr7:98027954-98027971 chr7:98027956-98027967
35	CHD2	chr7:98023786-98024105	Hela-S3	cervix:	n/a	n/a
36	CREB1	chr7:98027846-98028279	ECC-1	luminal epithelium:	n/a	n/a
37	CTCF	chr7:98028080-98028230	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr7:98028020-98028170	HepG2	liver:	n/a	n/a
39	CTCF	chr7:98028100-98028250	HMEC	breast:	n/a	n/a
40	CTCF	chr7:98028040-98028190	GM12873	blood:	n/a	n/a
41	CTCF	chr7:98028100-98028250	K562	blood:	n/a	n/a
42	CTCF	chr7:98010580-98010730	HRPEpiC	eye:	n/a	n/a
43	CUX1	chr7:98021929-98022018	K562	blood:	n/a	n/a
44	E2F4	chr7:98001222-98001284	MCF10A-Er-Src	breast:	n/a	n/a
45	EBF1	chr7:98007610-98007772	GM12878	blood:	n/a	n/a
46	EBF1	chr7:98027117-98027206	GM12878	blood:	n/a	n/a
47	EBF1	chr7:98010824-98010938	GM12878	blood:	n/a	n/a
48	EGR1	chr7:98004908-98005097	K562	blood:	n/a	n/a
49	ELF1	chr7:98028038-98028501	K562	blood:	n/a	n/a
50	EP300	chr7:98002236-98002854	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:98026481-98026531	ProgFib	skin:	n/a
2	chr7:98026481-98026531	ovcar-3	ovarian:	n/a
3	chr7:98026481-98026531	HepG2	liver:	n/a
4	chr7:98026481-98026531	K562	blood:	n/a
5	chr7:98026481-98026531	H1-hESC	embryonic stem cell:	embryo
6	chr7:98026481-98026531	HCPEpiC	choroid plexus:	n/a
7	chr7:98026481-98026531	SK-N-MC	brain:	n/a
8	chr7:98026481-98026531	HCT-116	colon:	n/a
9	chr7:98026481-98026531	A549	lung:	n/a
10	chr7:98026481-98026531	Hepatocyte	liver:	n/a
11	chr7:98026481-98026531	HIPEpiC	eye:	n/a
12	chr7:98026481-98026531	SK-N-SH_RA	brain:	n/a
13	chr7:98026481-98026531	IMR90	lung:	fetal
14	chr7:98026481-98026531	SK-N-SH	brain:	n/a
15	chr7:98026481-98026531	NHBE	bronchial:	n/a
16	chr7:98026481-98026531	NH-A	brain:	n/a
17	chr7:98026481-98026531	Caco-2	colon:	n/a
18	chr7:98026481-98026531	GM12891	blood:	n/a
19	chr7:98026481-98026531	HL-60	blood:	n/a
20	chr7:98026481-98026531	GM06990	blood:	n/a
21	chr7:98026481-98026531	Hela-S3	cervix:	n/a
22	chr7:98026481-98026531	HRCEpiC	kidney:	n/a
23	chr7:98026481-98026531	AG10803	skin:	n/a
24	chr7:98026481-98026531	HAEpiC	amniotic membrane:	n/a
25	chr7:98026481-98026531	AG04449	skin:	fetal
26	chr7:98026481-98026531	HMEC	breast:	n/a
27	chr7:98026481-98026531	U87	brain:	n/a
28	chr7:98026481-98026531	MCF-7	breast:	n/a
29	chr7:98026481-98026531	SAEC	small airway:	n/a
30	chr7:98026481-98026531	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:98026481-98026531	BJ	skin:	n/a
32	chr7:98026481-98026531	NB4	blood:	n/a
33	chr7:98026481-98026531	RPTEC	kidney:	n/a
34	chr7:98026481-98026531	HEK293	kidney:	embryo
35	chr7:98026481-98026531	HRPEpiC	eye:	n/a
36	chr7:98026481-98026531	BE2_C	brain:	n/a
37	chr7:98026481-98026531	GM19239	blood:	n/a
38	chr7:98026481-98026531	HRE	kidney:	n/a
39	chr7:98026481-98026531	AG04450	lung:	fetal
40	chr7:98026481-98026531	CMK	blood:	n/a
41	chr7:98026481-98026531	PANC-1	pancreas:	n/a
42	chr7:98026481-98026531	GM12878	blood:	n/a
43	chr7:98026481-98026531	AG09309	skin:	n/a
44	chr7:98026481-98026531	HCM	heart:	n/a
45	chr7:98026481-98026531	ECC-1	luminal epithelium:	n/a
46	chr7:98026481-98026531	SKMC	muscle:	n/a
47	chr7:98026481-98026531	NHDF-neo	bronchial:	n/a
48	chr7:98026481-98026531	HEEpiC	esophagus:	n/a
49	chr7:98026481-98026531	HCF	heart:	n/a
50	chr7:98026481-98026531	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:97851992..97854043-chr7:98027877..98030619,2	K562	blood:
2	chr7:98013767..98016196-chr7:98019830..98022730,2	K562	blood:
3	chr7:98023816..98025610-chr7:98048649..98050466,2	MCF-7	breast:
4	chr7:98008859..98010554-chr7:98015370..98018047,2	K562	blood:
5	chr7:98002220..98003756-chr7:98007556..98009163,2	K562	blood:
6	chr7:97948846..97953573-chr7:98026962..98031463,6	MCF-7	breast:
7	chr7:97998858..98000704-chr7:98027178..98028821,2	MCF-7	breast:
8	chr7:97923208..97926071-chr7:98023782..98025314,2	K562	blood:
9	chr7:98018093..98019903-chr7:98028373..98029926,2	MCF-7	breast:
10	chr7:98023392..98027153-chr7:98028051..98031906,5	K562	blood:
11	chr7:98002220..98003756-chr7:98007556..98009163,2	K562	blood:
12	chr7:98011872..98013526-chr7:98027965..98030141,2	MCF-7	breast:
13	chr7:98023705..98027880-chr7:98028270..98031310,4	MCF-7	breast:
14	chr7:97998858..98000704-chr7:98027178..98028821,2	MCF-7	breast:
15	chr7:97948534..97953392-chr7:98027922..98031084,5	MCF-7	breast:
16	chr7:97987419..97989875-chr7:98026560..98028581,2	K562	blood:
17	chr7:97983585..97986077-chr7:98010097..98011700,2	MCF-7	breast:
18	chr7:97985772..97988094-chr7:97995207..97997337,2	K562	blood:
19	chr7:98015865..98017595-chr7:98028896..98031691,2	MCF-7	breast:
20	chr7:98023392..98026419-chr7:98028385..98032176,4	K562	blood:

Variant related genes	Relation type
RPS3AP26	TF binding region
RPS3AP26	CpG island
ENSG00000006453	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000272950	chromatin interactions
ENSG00000214389	chromatin interactions

Extended variants
information (count: 1363 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1363 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546023733	chr7:97995969-97995970	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs140809572	chr7:97995996-97995997	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs191765330	chr7:97996020-97996021	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs373349136	chr7:97996021-97996022	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs184177858	chr7:97996052-97996053	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs538122909	chr7:97996054-97996055	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs77503082	chr7:97996055-97996056	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs529324242	chr7:97996099-97996100	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs188972931	chr7:97996132-97996133	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs192249821	chr7:97996251-97996252	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539503572	chr7:97996253-97996254	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4729433	chr7:97996254-97996255	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs55718604	chr7:97996292-97996293	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368904197	chr7:97996370-97996371	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs386410796	chr7:97996371-97996372	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs71292948	chr7:97996386-97996387	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534103167	chr7:97996468-97996469	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556058676	chr7:97996549-97996550	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574214779	chr7:97996564-97996565	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6968222	chr7:97996570-97996571	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs4236537	chr7:97996593-97996594	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs200431179	chr7:97996650-97996651	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575421007	chr7:97996674-97996675	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370733426	chr7:97996683-97996684	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545954597	chr7:97996725-97996726	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564148040	chr7:97996731-97996732	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375503324	chr7:97996776-97996777	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185661519	chr7:97996829-97996830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35449156	chr7:97996863-97996864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34472020	chr7:97996864-97996865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs34018144	chr7:97996865-97996866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529126791	chr7:97996879-97996880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550972774	chr7:97996887-97996888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372130950	chr7:97996905-97996906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533137948	chr7:97996914-97996915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111318271	chr7:97996916-97996917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190490306	chr7:97996918-97996919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2894172	chr7:97996957-97996958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180824028	chr7:97996980-97996981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549265632	chr7:97997004-97997005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553839769	chr7:97997005-97997006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567972705	chr7:97997008-97997009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186050200	chr7:97997011-97997012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149012247	chr7:97997057-97997058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188499035	chr7:97997064-97997065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6969160	chr7:97997091-97997092	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs181318408	chr7:97997093-97997094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572036438	chr7:97997133-97997134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs62478201	chr7:97997164-97997165	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs540423784	chr7:97997215-97997216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97977200-98010200	Weak transcription	GM12878-XiMat	blood
2	chr7:97984800-98000200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:97984800-98002200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr7:97990000-97998400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:97990400-98017200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:97990400-98028000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:97990600-98010400	Weak transcription	HepG2	liver
8	chr7:97991000-97999200	Weak transcription	Hela-S3	cervix
9	chr7:97991000-98002200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr7:97992000-97996000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:97992000-97998400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr7:97992000-98000200	Weak transcription	HMEC	breast
13	chr7:97992000-98029400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:97992200-97999200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr7:97992800-98017400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:97993200-97998800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:97993800-98005400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr7:97994200-97998200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr7:97994600-98000600	Enhancers	Stomach Mucosa	stomach
20	chr7:97994800-97996400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:97995000-97997800	Weak transcription	Gastric	stomach
22	chr7:97995200-97996000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr7:97995200-97996000	Enhancers	HUVEC	blood vessel
24	chr7:97995200-97996200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr7:97995200-97996400	Strong transcription	Fetal Intestine Small	intestine
26	chr7:97995400-97996200	Enhancers	Duodenum Mucosa	Duodenum
27	chr7:97995400-97996200	Enhancers	Left Ventricle	heart
28	chr7:97995400-97996200	Enhancers	Lung	lung
29	chr7:97995400-97996200	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr7:97995400-97996400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:97995400-97996400	Strong transcription	A549	lung
32	chr7:97995600-97996200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:97995600-97996200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr7:97995600-97996200	Enhancers	Fetal Muscle Leg	muscle
35	chr7:97995600-97996200	Enhancers	Placenta	Placenta
36	chr7:97995600-97996200	Enhancers	Spleen	Spleen
37	chr7:97995600-97999400	Weak transcription	Osteobl	bone
38	chr7:97995600-98002400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr7:97995600-98002400	Weak transcription	NH-A	brain
40	chr7:97995800-97996800	Strong transcription	NHEK	skin
41	chr7:97995800-97998600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:97995800-98000200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:97995800-98000200	Weak transcription	Pancreas	Pancrea
44	chr7:97995800-98028200	Weak transcription	Esophagus	oesophagus
45	chr7:97996000-97996200	Enhancers	Adipose Nuclei	Adipose
46	chr7:97996000-97996400	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr7:97996000-97998200	Weak transcription	HUVEC	blood vessel
48	chr7:97996000-98000200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:97996200-97997800	Weak transcription	Fetal Muscle Leg	muscle
50	chr7:97996200-97998000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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