Variant report

Variant	nsv869741
Chromosome Location	chr7:100977907-101132601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2177)
CpG islands
(count:1651)
Chromatin interactive
region (count:75)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2177 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101054542-101054748	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:101034275-101034431	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101029701-101030402	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:101041212-101041406	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:100995510-100995986	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:100995557-100996013	K562	blood:	n/a	n/a
7	ATF1	chr7:100995667-100996035	K562	blood:	n/a	n/a
8	ATF2	chr7:101054507-101054909	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:101034206-101034498	GM12878	blood:	n/a	n/a
10	ATF2	chr7:101045113-101045819	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:101045260-101045884	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:101007153-101007579	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:101034154-101034562	GM12878	blood:	n/a	n/a
14	ATF2	chr7:101005691-101006042	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:100995608-100996147	K562	blood:	n/a	n/a
16	ATF3	chr7:101083791-101083930	K562	blood:	n/a	n/a
17	BACH1	chr7:101006064-101006399	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:101045151-101045712	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:101042008-101042270	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:100978932-100978958	K562	blood:	n/a	n/a
21	BACH1	chr7:101006969-101007517	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:101083766-101083964	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:101054392-101054843	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:101080560-101080609	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr7:101034127-101034558	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:101045447-101045692	H1-hESC	embryonic stem cell:	n/a	chr7:101045565-101045572 chr7:101045573-101045582
27	BCL3	chr7:101045252-101045835	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
28	BCL3	chr7:101071831-101072136	GM12878	blood:	n/a	n/a
29	BCL3	chr7:101085899-101086361	GM12878	blood:	n/a	n/a
30	BCL3	chr7:101085919-101086314	GM12878	blood:	n/a	n/a
31	BCL3	chr7:100995424-100996093	A549	lung:	n/a	chr7:100995867-100995874
32	BCL3	chr7:101045065-101045790	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
33	BCL3	chr7:100995430-100996053	A549	lung:	n/a	chr7:100995867-100995874
34	BCL3	chr7:101006990-101007617	A549	lung:	n/a	chr7:101007240-101007249 chr7:101007424-101007437
35	BCL3	chr7:101034235-101034520	GM12878	blood:	n/a	n/a
36	BCL3	chr7:101071768-101072139	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:101083725-101083894	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:100995649-100996149	K562	blood:	n/a	n/a
39	BHLHE40	chr7:101007069-101007443	K562	blood:	n/a	n/a
40	BHLHE40	chr7:101034158-101034493	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:101054571-101054732	K562	blood:	n/a	n/a
42	BHLHE40	chr7:101085990-101086330	K562	blood:	n/a	n/a
43	BHLHE40	chr7:101006937-101007505	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:101007335-101007606	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:100995806-100995888	HepG2	liver:	n/a	n/a
46	BRCA1	chr7:101034269-101034281	HepG2	liver:	n/a	n/a
47	BRCA1	chr7:101030201-101030430	HepG2	liver:	n/a	n/a
48	BRCA1	chr7:100996299-100996395	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr7:101034222-101034342	GM12878	blood:	n/a	n/a
50	CBX3	chr7:101122526-101122848	K562	blood:	n/a	n/a

(count:1651 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101006573-101006623	RPTEC	kidney:	n/a
2	chr7:101007072-101007122	HepG2	liver:	n/a
3	chr7:101006573-101006623	MCF-7	breast:	n/a
4	chr7:101006963-101007013	ovcar-3	ovarian:	n/a
5	chr7:101006573-101006623	RPTEC	kidney:	n/a
6	chr7:101007072-101007122	HepG2	liver:	n/a
7	chr7:101006573-101006623	MCF-7	breast:	n/a
8	chr7:101006963-101007013	ovcar-3	ovarian:	n/a
9	chr7:101005832-101005882	LNCaP	prostate:	n/a
10	chr7:101007442-101007492	NB4	blood:	n/a
11	chr7:101132009-101132059	GM06990	blood:	n/a
12	chr7:101054654-101054704	PANC-1	pancreas:	n/a
13	chr7:101049300-101049350	Hepatocyte	liver:	n/a
14	chr7:101006052-101006102	HRE	kidney:	n/a
15	chr7:101054654-101054704	AG09309	skin:	n/a
16	chr7:101129980-101130030	PrEC	prostate:	n/a
17	chr7:101006063-101006113	SKMC	muscle:	n/a
18	chr7:101005832-101005882	PrEC	prostate:	n/a
19	chr7:101005846-101005896	NB4	blood:	n/a
20	chr7:101129980-101130030	SK-N-MC	brain:	n/a
21	chr7:100993034-100993084	GM06990	blood:	n/a
22	chr7:101054654-101054704	GM12892	blood:	n/a
23	chr7:101007190-101007240	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:101049372-101049422	NH-A	brain:	n/a
25	chr7:101007442-101007492	NH-A	brain:	n/a
26	chr7:101006089-101006139	GM12891	blood:	n/a
27	chr7:101007072-101007122	HCM	heart:	n/a
28	chr7:101006052-101006102	HAEpiC	amniotic membrane:	n/a
29	chr7:101017354-101017404	ovcar-3	ovarian:	n/a
30	chr7:101006052-101006102	Caco-2	colon:	n/a
31	chr7:101005832-101005882	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:101129980-101130030	NHDF-neo	bronchial:	n/a
33	chr7:101079617-101079667	BJ	skin:	n/a
34	chr7:101007072-101007122	AoSMC	blood vessel:	n/a
35	chr7:101054654-101054704	HCF	heart:	n/a
36	chr7:100993034-100993084	HRE	kidney:	n/a
37	chr7:101006308-101006358	AoSMC	blood vessel:	n/a
38	chr7:101063331-101063381	SKMC	muscle:	n/a
39	chr7:101007190-101007240	HMEC	breast:	n/a
40	chr7:101005910-101005960	Jurkat	blood:	n/a
41	chr7:101079617-101079667	Caco-2	colon:	n/a
42	chr7:101017354-101017404	HUVEC	blood vessel:	n/a
43	chr7:101007442-101007492	AG04450	lung:	fetal
44	chr7:101006058-101006108	NHBE	bronchial:	n/a
45	chr7:101006573-101006623	HCM	heart:	n/a
46	chr7:101006963-101007013	GM12892	blood:	n/a
47	chr7:100993034-100993084	GM19239	blood:	n/a
48	chr7:101006035-101006085	H1-hESC	embryonic stem cell:	embryo
49	chr7:101005910-101005960	MCF10A-Er-Src	breast:	n/a
50	chr7:101006963-101007013	GM06990	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
2	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
3	chr7:101083724..101084446-chr7:101150709..101151315,2	MCF-7	breast:
4	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
5	chr7:101032377..101034733-chr7:101037402..101040388,2	MCF-7	breast:
6	chr7:100949900..100952097-chr7:100994165..100995851,2	MCF-7	breast:
7	chr7:101043147..101045492-chr7:101051053..101052921,2	K562	blood:
8	chr7:101012360..101015108-chr7:101017249..101019175,2	K562	blood:
9	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
10	chr7:101006862..101007822-chr7:101083395..101084349,8	MCF-7	breast:
11	chr7:101100607..101102049-chr7:101150824..101151606,9	MCF-7	breast:
12	chr7:101037193..101039012-chr7:101045881..101047459,2	MCF-7	breast:
13	chr7:101115888..101118705-chr7:101119430..101120969,2	MCF-7	breast:
14	chr7:101006441..101008974-chr7:101023704..101025266,2	MCF-7	breast:
15	chr12:132413848..132415692-chr7:101084473..101086964,2	MCF-7	breast:
16	chr7:101015968..101018340-chr7:101024306..101026455,2	MCF-7	breast:
17	chr7:101006746..101007872-chr7:101054217..101055171,4	K562	blood:
18	chr7:101023195..101025977-chr7:101028738..101030293,2	K562	blood:
19	chr7:101015968..101018340-chr7:101024306..101026455,2	MCF-7	breast:
20	chr7:101131107..101133497-chr7:101133742..101135419,2	K562	blood:
21	chr7:101012360..101015108-chr7:101017249..101019175,2	K562	blood:
22	chr7:101041365..101043542-chr7:101048323..101050814,2	MCF-7	breast:
23	chr7:101006939..101007476-chr7:101083770..101084337,2	K562	blood:
24	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
25	chr7:101007762..101011060-chr7:101013667..101017793,3	K562	blood:
26	chr7:101023195..101025977-chr7:101028738..101030293,2	K562	blood:
27	chr7:101006932..101008338-chr7:101181516..101182765,6	K562	blood:
28	chr7:100963124..100966014-chr7:101122778..101124584,2	MCF-7	breast:
29	chr7:101054216..101055052-chr7:101150685..101151359,3	MCF-7	breast:
30	chr7:101007762..101011060-chr7:101013667..101017793,3	K562	blood:
31	chr7:101006811..101007905-chr7:101150693..101151800,11	K562	blood:
32	chr7:101006530..101007875-chr7:101054200..101055148,9	MCF-7	breast:
33	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
34	chr7:101043147..101045492-chr7:101051053..101052921,2	K562	blood:
35	chr7:100989055..100991707-chr7:100994198..100995736,2	MCF-7	breast:
36	chr7:101112161..101112969-chr7:101150803..101151689,2	MCF-7	breast:
37	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
38	chr7:101039985..101042024-chr7:101043789..101046579,2	MCF-7	breast:
39	chr7:101068095..101068916-chr7:101150848..101151469,2	MCF-7	breast:
40	chr7:101022613..101024114-chr7:101025793..101027679,2	MCF-7	breast:
41	chr7:100964942..100967208-chr7:101081876..101083958,2	MCF-7	breast:
42	chr7:101031371..101033701-chr7:101034998..101036873,2	K562	blood:
43	chr7:101006510..101007838-chr7:101150604..101151700,15	MCF-7	breast:
44	chr7:100964752..100967137-chr7:100978107..100980737,2	MCF-7	breast:
45	chr7:101006995..101008302-chr7:101082934..101084354,6	MCF-7	breast:
46	chr7:101115888..101118705-chr7:101119430..101120969,2	MCF-7	breast:
47	chr7:101022613..101024114-chr7:101025793..101027679,2	MCF-7	breast:
48	chr7:101100597..101102046-chr7:101150673..101151702,7	MCF-7	breast:
49	chr7:101037193..101039012-chr7:101045881..101047459,2	MCF-7	breast:
50	chr7:101067571..101069515-chr7:101079650..101082212,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABL5-1	chr7:100995310-100996633	ucscGeneNc_uc003uyp_2
2	lnc-RABL5-2	chr7:101032149-101032361	NONHSAT122467
3	lnc-RABL5-1	chr7:100998850-100999006	ucscGeneNc_uc003uyp_2

No data

Variant related genes	Relation type
ENSG00000233683	TF binding region
COL26A1	TF binding region
ENSG00000233683	CpG island
COL26A1	CpG island
ENSG00000232445	chromatin interactions
ENSG00000177192	chromatin interactions
ENSG00000233683	chromatin interactions
ENSG00000128581	chromatin interactions
ENSG00000160963	chromatin interactions
ENSG00000255992	chromatin interactions

Extended variants
information (count: 6808 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6808 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188983509	chr7:100977931-100977932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567605848	chr7:100977940-100977941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192951587	chr7:100977970-100977971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143285098	chr7:100978013-100978014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73713869	chr7:100978029-100978030	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs539013051	chr7:100978167-100978168	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs67736913	chr7:100978174-100978175	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs141372476	chr7:100978186-100978187	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs10684144	chr7:100978212-100978213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572563764	chr7:100978214-100978215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34872936	chr7:100978261-100978262	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs140069651	chr7:100978262-100978263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560345313	chr7:100978288-100978289	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543688317	chr7:100978302-100978303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184598796	chr7:100978317-100978318	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs527878469	chr7:100978333-100978334	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs367815148	chr7:100978334-100978335	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188608662	chr7:100978353-100978354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557448659	chr7:100978368-100978369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565549157	chr7:100978412-100978413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532710537	chr7:100978413-100978414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181682640	chr7:100978423-100978424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1962160	chr7:100978430-100978431	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs558930389	chr7:100978439-100978440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs13240188	chr7:100978444-100978445	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs113221532	chr7:100978451-100978452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377289337	chr7:100978474-100978475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372919458	chr7:100978484-100978485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs13240202	chr7:100978485-100978486	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs370168511	chr7:100978520-100978521	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570757121	chr7:100978530-100978531	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs534958646	chr7:100978538-100978539	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs554168793	chr7:100978540-100978541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374533817	chr7:100978583-100978584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs6465796	chr7:100978587-100978588	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs189510069	chr7:100978607-100978608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181934553	chr7:100978654-100978655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543990188	chr7:100978663-100978664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186174329	chr7:100978687-100978688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7456831	chr7:100978688-100978689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs577080826	chr7:100978701-100978702	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs541327202	chr7:100978722-100978723	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs190647388	chr7:100978742-100978743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138854042	chr7:100978747-100978748	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs541497582	chr7:100978758-100978759	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs77705811	chr7:100978782-100978783	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs143075670	chr7:100978784-100978785	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182774798	chr7:100978849-100978850	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535572367	chr7:100978865-100978866	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34967268	chr7:100978876-100978877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	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
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1921 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100973600-100980600	Weak transcription	Right Atrium	heart
2	chr7:100977400-100978200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:100982400-100983800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:100983800-100984000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:100984000-100990800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:100990800-100991200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:100990800-100991400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:100991000-101006000	Weak transcription	Right Atrium	heart
9	chr7:100991200-100991400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:100991400-100992800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:100991400-100993000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:100992800-100993000	Enhancers	Stomach Mucosa	stomach
13	chr7:100992800-100993200	Enhancers	K562	blood
14	chr7:100992800-100993400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:100992800-100993400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr7:100993000-100993200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:100993000-100994000	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr7:100993200-100993400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr7:100993200-100993400	Enhancers	HepG2	liver
20	chr7:100993200-100993400	Flanking Active TSS	K562	blood
21	chr7:100993400-100994800	Weak transcription	K562	blood
22	chr7:100993400-100995000	Weak transcription	HepG2	liver
23	chr7:100993400-100995600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr7:100993400-101005400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:100994000-100995600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr7:100994600-100995200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr7:100994800-100995400	Enhancers	A549	lung
28	chr7:100994800-100996000	Enhancers	Stomach Mucosa	stomach
29	chr7:100994800-100996400	Enhancers	K562	blood
30	chr7:100995000-100995200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:100995000-100995400	Enhancers	Hela-S3	cervix
32	chr7:100995000-100996400	Enhancers	Liver	Liver
33	chr7:100995000-100996400	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr7:100995000-100996600	Enhancers	HepG2	liver
35	chr7:100995200-101005600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:100995400-100995800	Enhancers	Fetal Intestine Large	intestine
37	chr7:100995400-100995800	Enhancers	Fetal Muscle Leg	muscle
38	chr7:100995400-100996000	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr7:100995400-100996000	Enhancers	Fetal Intestine Small	intestine
40	chr7:100995400-100996000	Flanking Active TSS	A549	lung
41	chr7:100995400-100996200	Flanking Active TSS	Hela-S3	cervix
42	chr7:100995600-100995800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr7:100995600-100995800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr7:100995600-100996000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr7:100995600-100996000	Enhancers	Duodenum Mucosa	Duodenum
46	chr7:100995600-100996200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr7:100995800-100996000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr7:100996000-100996400	Enhancers	A549	lung
49	chr7:100996200-100996600	Enhancers	Hela-S3	cervix
50	chr7:100996400-101000200	Weak transcription	Liver	Liver

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