Variant report

Variant	nsv1017544
Chromosome Location	chr7:100965601-101116322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2363)
CpG islands
(count:1832)
Chromatin interactive
region (count:79)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2363 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101034275-101034431	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:101041212-101041406	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:101029701-101030402	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:100995557-100996013	K562	blood:	n/a	n/a
5	ARID3A	chr7:101054542-101054748	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:100995510-100995986	HepG2	liver:	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	chr7:101045260-101045884	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:101034154-101034562	GM12878	blood:	n/a	n/a
11	ATF2	chr7:101005691-101006042	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	chr7:101045113-101045819	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:101034206-101034498	GM12878	blood:	n/a	n/a
15	ATF3	chr7:101083791-101083930	K562	blood:	n/a	n/a
16	ATF3	chr7:100995608-100996147	K562	blood:	n/a	n/a
17	BACH1	chr7:101080560-101080609	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:101006064-101006399	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:100978932-100978958	K562	blood:	n/a	n/a
20	BACH1	chr7:101054392-101054843	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:101083766-101083964	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:101006969-101007517	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:101045151-101045712	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:101042008-101042270	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	chr7:101071768-101072139	GM12878	blood:	n/a	n/a
28	BCL3	chr7:101006990-101007617	A549	lung:	n/a	chr7:101007240-101007249 chr7:101007424-101007437
29	BCL3	chr7:100995424-100996093	A549	lung:	n/a	chr7:100995867-100995874
30	BCL3	chr7:101085899-101086361	GM12878	blood:	n/a	n/a
31	BCL3	chr7:101071831-101072136	GM12878	blood:	n/a	n/a
32	BCL3	chr7:101085919-101086314	GM12878	blood:	n/a	n/a
33	BCL3	chr7:101045065-101045790	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
34	BCL3	chr7:101045252-101045835	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
35	BCL3	chr7:101034235-101034520	GM12878	blood:	n/a	n/a
36	BCL3	chr7:100995430-100996053	A549	lung:	n/a	chr7:100995867-100995874
37	BHLHE40	chr7:101083725-101083894	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:101085990-101086330	K562	blood:	n/a	n/a
39	BHLHE40	chr7:101007069-101007443	K562	blood:	n/a	n/a
40	BHLHE40	chr7:101007335-101007606	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:101006937-101007505	HepG2	liver:	n/a	n/a
42	BHLHE40	chr7:101034158-101034493	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:100995806-100995888	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:101054571-101054732	K562	blood:	n/a	n/a
45	BHLHE40	chr7:100995649-100996149	K562	blood:	n/a	n/a
46	BRCA1	chr7:101034222-101034342	GM12878	blood:	n/a	n/a
47	BRCA1	chr7:100996299-100996395	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr7:101034269-101034281	HepG2	liver:	n/a	n/a
49	BRCA1	chr7:101030201-101030430	HepG2	liver:	n/a	n/a
50	CBX3	chr7:101054500-101054959	K562	blood:	n/a	n/a

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101006963-101007013	GM19239	blood:	n/a
2	chr7:101006035-101006085	H1-hESC	embryonic stem cell:	embryo
3	chr7:101006963-101007013	GM19239	blood:	n/a
4	chr7:101006035-101006085	H1-hESC	embryonic stem cell:	embryo
5	chr7:101049300-101049350	SAEC	small airway:	n/a
6	chr7:100968383-100968433	HAEpiC	amniotic membrane:	n/a
7	chr7:100993034-100993084	BJ	skin:	n/a
8	chr7:101006058-101006108	BJ	skin:	n/a
9	chr7:101006063-101006113	HCM	heart:	n/a
10	chr7:101079617-101079667	AG09319	gingival:	n/a
11	chr7:101054654-101054704	BJ	skin:	n/a
12	chr7:101007072-101007122	Hela-S3	cervix:	n/a
13	chr7:101005846-101005896	NHDF-neo	bronchial:	n/a
14	chr7:100965680-100965730	SK-N-SH_RA	brain:	n/a
15	chr7:101006058-101006108	RPTEC	kidney:	n/a
16	chr7:100965709-100965759	AoSMC	blood vessel:	n/a
17	chr7:101049372-101049422	MCF10A-Er-Src	breast:	n/a
18	chr7:101017354-101017404	HCM	heart:	n/a
19	chr7:101079617-101079667	SK-N-MC	brain:	n/a
20	chr7:101007442-101007492	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:101079617-101079667	AG04450	lung:	fetal
22	chr7:101006363-101006413	PANC-1	pancreas:	n/a
23	chr7:101055912-101055962	NH-A	brain:	n/a
24	chr7:101006058-101006108	HRCEpiC	kidney:	n/a
25	chr7:101006035-101006085	HAEpiC	amniotic membrane:	n/a
26	chr7:101054654-101054704	NH-A	brain:	n/a
27	chr7:100965709-100965759	GM06990	blood:	n/a
28	chr7:100966076-100966126	AG09319	gingival:	n/a
29	chr7:100993034-100993084	NT2-D1	testis:	n/a
30	chr7:101007442-101007492	HepG2	liver:	n/a
31	chr7:101007190-101007240	HMEC	breast:	n/a
32	chr7:101006573-101006623	ovcar-3	ovarian:	n/a
33	chr7:101049372-101049422	HCPEpiC	choroid plexus:	n/a
34	chr7:101007442-101007492	AG04449	skin:	fetal
35	chr7:101054654-101054704	AG09319	gingival:	n/a
36	chr7:101049300-101049350	K562	blood:	n/a
37	chr7:101063331-101063381	Jurkat	blood:	n/a
38	chr7:101006035-101006085	A549	lung:	n/a
39	chr7:101007072-101007122	GM19239	blood:	n/a
40	chr7:100965680-100965730	SAEC	small airway:	n/a
41	chr7:100965709-100965759	PFSK-1	brain:	n/a
42	chr7:101006363-101006413	SK-N-SH	brain:	n/a
43	chr7:101006019-101006069	HCM	heart:	n/a
44	chr7:100993034-100993084	CMK	blood:	n/a
45	chr7:100993034-100993084	GM12878	blood:	n/a
46	chr7:100966076-100966126	CMK	blood:	n/a
47	chr7:100966078-100966128	Jurkat	blood:	n/a
48	chr7:101007442-101007492	ovcar-3	ovarian:	n/a
49	chr7:101006308-101006358	AG09319	gingival:	n/a
50	chr7:100966076-100966126	Hepatocyte	liver:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:101006995..101008302-chr7:101082934..101084354,6	MCF-7	breast:
2	chr7:101006908..101008057-chr7:101150804..101151679,7	MCF-7	breast:
3	chr7:101022613..101024114-chr7:101025793..101027679,2	MCF-7	breast:
4	chr7:101112161..101112969-chr7:101150803..101151689,2	MCF-7	breast:
5	chr7:101041365..101043542-chr7:101048323..101050814,2	MCF-7	breast:
6	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
7	chr7:100964752..100967137-chr7:100978107..100980737,2	MCF-7	breast:
8	chr7:101068095..101068916-chr7:101150848..101151469,2	MCF-7	breast:
9	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
10	chr12:132413848..132415692-chr7:101084473..101086964,2	MCF-7	breast:
11	chr7:100965037..100965724-chr9:89562019..89562831,2	Hela-S3	cervix:
12	chr7:101110378..101112867-chr7:101115903..101117438,2	K562	blood:
13	chr7:101007762..101011060-chr7:101013667..101017793,3	K562	blood:
14	chr7:101032377..101034733-chr7:101037402..101040388,2	MCF-7	breast:
15	chr7:101022613..101024114-chr7:101025793..101027679,2	MCF-7	breast:
16	chr7:101031371..101033701-chr7:101034998..101036873,2	K562	blood:
17	chr7:100964710..100967141-chr7:101003077..101007417,4	MCF-7	breast:
18	chr7:101039985..101042024-chr7:101043789..101046579,2	MCF-7	breast:
19	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
20	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
21	chr7:101084569..101086934-chr7:101141583..101143364,2	MCF-7	breast:
22	chr7:100965612..100969667-chr7:101005034..101007660,3	MCF-7	breast:
23	chr7:101041365..101043542-chr7:101048323..101050814,2	MCF-7	breast:
24	chr7:101054216..101055052-chr7:101150685..101151359,3	MCF-7	breast:
25	chr15:65596698..65597638-chr7:100964826..100965617,2	HCT-116	colon:
26	chr7:100964942..100967208-chr7:101081876..101083958,2	MCF-7	breast:
27	chr7:101015968..101018340-chr7:101024306..101026455,2	MCF-7	breast:
28	chr7:101005587..101007184-chr7:101013675..101015580,2	MCF-7	breast:
29	chr7:101006932..101008338-chr7:101181516..101182765,6	K562	blood:
30	chr7:100989055..100991707-chr7:100994198..100995736,2	MCF-7	breast:
31	chr7:101032377..101034733-chr7:101037402..101040388,2	MCF-7	breast:
32	chr7:101006939..101007476-chr7:101083770..101084337,2	K562	blood:
33	chr7:101100597..101102046-chr7:101150673..101151702,7	MCF-7	breast:
34	chr7:101016391..101018815-chr7:101033017..101035506,2	K562	blood:
35	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
36	chr7:101067571..101069515-chr7:101079650..101082212,2	MCF-7	breast:
37	chr7:101006862..101007822-chr7:101083395..101084349,8	MCF-7	breast:
38	chr7:101006746..101007872-chr7:101054217..101055171,4	K562	blood:
39	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
40	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
41	chr7:101067571..101069515-chr7:101079650..101082212,2	MCF-7	breast:
42	chr7:101006530..101007875-chr7:101054200..101055148,9	MCF-7	breast:
43	chr7:101083863..101087245-chr7:101089520..101092470,3	K562	blood:
44	chr7:101039985..101042024-chr7:101043789..101046579,2	MCF-7	breast:
45	chr7:100964710..100967141-chr7:101003077..101007417,4	MCF-7	breast:
46	chr7:101043147..101045492-chr7:101051053..101052921,2	K562	blood:
47	chr7:101006746..101007872-chr7:101054217..101055171,4	K562	blood:
48	chr7:100989055..100991707-chr7:100994198..100995736,2	MCF-7	breast:
49	chr7:101007762..101011060-chr7:101013667..101017793,3	K562	blood:
50	chr7:101006995..101008302-chr7:101082934..101084354,6	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
RABL5	TF binding region
ENSG00000233683	TF binding region
COL26A1	TF binding region
RABL5	CpG island
ENSG00000233683	CpG island
COL26A1	CpG island
ENSG00000232445	chromatin interactions
ENSG00000180447	chromatin interactions
ENSG00000177192	chromatin interactions
ENSG00000255992	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000128581	chromatin interactions
ENSG00000160963	chromatin interactions
ENSG00000233683	chromatin interactions

Extended variants
information (count: 6608 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6608 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3807513	chr7:100965601-100965602	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367940357	chr7:100965641-100965642	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs181022323	chr7:100965649-100965650	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs58513532	chr7:100965733-100965734	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs370001814	chr7:100965776-100965777	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs3807514	chr7:100965789-100965790	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs535277116	chr7:100965810-100965811	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs147956779	chr7:100965930-100965931	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs116570375	chr7:100965943-100965944	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs569153770	chr7:100965959-100965960	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs539788563	chr7:100965997-100965998	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs558668405	chr7:100966057-100966058	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs577176362	chr7:100966077-100966078	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs534760349	chr7:100966079-100966080	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs185051249	chr7:100966125-100966126	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs201926042	chr7:100966194-100966195	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs71129604	chr7:100966196-100966197	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs66989903	chr7:100966197-100966198	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs199779468	chr7:100966211-100966212	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs115905454	chr7:100966238-100966239	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs552731364	chr7:100966243-100966244	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574656294	chr7:100966250-100966251	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs542002555	chr7:100966256-100966257	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs116253078	chr7:100966262-100966263	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs572053765	chr7:100966266-100966267	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs190144742	chr7:100966335-100966336	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs375472633	chr7:100966348-100966349	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563881259	chr7:100966362-100966363	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs528111490	chr7:100966371-100966372	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs13234919	chr7:100966372-100966373	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs4729688	chr7:100966407-100966408	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529029207	chr7:100966467-100966468	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs571767487	chr7:100966533-100966534	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs2410818	chr7:100966571-100966572	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs2410819	chr7:100966578-100966579	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs539078779	chr7:100966607-100966608	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112353669	chr7:100966616-100966617	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs182377710	chr7:100966622-100966623	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs186863188	chr7:100966634-100966635	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542483325	chr7:100966673-100966674	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535030978	chr7:100966715-100966716	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs113012083	chr7:100966727-100966728	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11298073	chr7:100966741-100966742	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553125796	chr7:100966746-100966747	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191700720	chr7:100966784-100966785	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183360846	chr7:100966805-100966806	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs557093092	chr7:100966817-100966818	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560780238	chr7:100966854-100966855	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs528292249	chr7:100966870-100966871	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs546359778	chr7:100966921-100966922	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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

Chromatin state (count:1968 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100964000-100965800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:100964000-100965800	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr7:100964000-100966000	Active TSS	H1 Cell Line	embryonic stem cell
4	chr7:100964000-100966000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:100964200-100965800	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr7:100964200-100965800	Active TSS	Primary T cells from cord blood	blood
7	chr7:100964200-100965800	Active TSS	Fetal Brain Female	brain
8	chr7:100964200-100965800	Active TSS	Rectal Smooth Muscle	rectum
9	chr7:100964200-100966000	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr7:100964200-100966000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:100964400-100965800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr7:100964400-100965800	Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr7:100964400-100965800	Active TSS	Fetal Intestine Large	intestine
14	chr7:100964400-100965800	Active TSS	Right Atrium	heart
15	chr7:100964400-100965800	Active TSS	NH-A	brain
16	chr7:100964400-100966000	Active TSS	H9 Cell Line	embryonic stem cell
17	chr7:100964400-100966000	Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr7:100964400-100966000	Active TSS	A549	lung
19	chr7:100964600-100965800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr7:100964600-100965800	Flanking Active TSS	Primary hematopoietic stem cells	blood
21	chr7:100964600-100965800	Active TSS	Aorta	Aorta
22	chr7:100964600-100965800	Active TSS	Brain Germinal Matrix	brain
23	chr7:100964600-100965800	Active TSS	Psoas Muscle	Psoas
24	chr7:100964600-100965800	Active TSS	K562	blood
25	chr7:100964600-100966200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:100964800-100965800	Active TSS	Colonic Mucosa	Colon
27	chr7:100964800-100965800	Active TSS	Right Ventricle	heart
28	chr7:100964800-100966000	Active TSS	Brain Angular Gyrus	brain
29	chr7:100964800-100966000	Active TSS	Duodenum Mucosa	Duodenum
30	chr7:100965000-100966000	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr7:100965000-100966200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:100965200-100965800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
33	chr7:100965200-100965800	Flanking Active TSS	Primary B cells from peripheral blood	blood
34	chr7:100965200-100965800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr7:100965200-100966000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:100965200-100966000	Flanking Active TSS	Dnd41	blood
37	chr7:100965400-100965800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr7:100965400-100965800	Flanking Active TSS	Primary B cells from cord blood	blood
39	chr7:100965400-100965800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
40	chr7:100965400-100965800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
41	chr7:100965400-100965800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr7:100965400-100965800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr7:100965400-100965800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr7:100965400-100965800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
45	chr7:100965400-100965800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr7:100965400-100965800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr7:100965400-100965800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr7:100965400-100965800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr7:100965400-100965800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:100965400-100965800	Flanking Active TSS	Adipose Nuclei	Adipose

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