Variant report

Variant	esv3375506
Chromosome Location	chr10:99078187-99080735
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	ARID3A	chr10:99078685-99079065	K562	blood:	n/a	n/a
2	ARID3A	chr10:99078577-99079081	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:99079935-99080002	HepG2	liver:	n/a	n/a
4	ATF1	chr10:99078580-99079153	K562	blood:	n/a	n/a
5	ATF2	chr10:99078438-99079187	H1-hESC	embryonic stem cell:	n/a	chr10:99078981-99078992
6	ATF2	chr10:99078393-99079195	H1-hESC	embryonic stem cell:	n/a	chr10:99078981-99078992
7	ATF2	chr10:99078567-99079208	GM12878	blood:	n/a	chr10:99078981-99078992
8	ATF2	chr10:99078597-99079142	GM12878	blood:	n/a	chr10:99078981-99078992
9	ATF3	chr10:99078749-99079156	K562	blood:	n/a	chr10:99078980-99078993 chr10:99078983-99078994 chr10:99078982-99078993 chr10:99078982-99078990 chr10:99078981-99078992 chr10:99078980-99078993 chr10:99078983-99078991 chr10:99078979-99078992 chr10:99078983-99078990 chr10:99078980-99078990 chr10:99078981-99078992 chr10:99078979-99078994
10	ATF3	chr10:99078639-99079083	A549	lung:	n/a	chr10:99078980-99078993 chr10:99078983-99078994 chr10:99078982-99078993 chr10:99078982-99078990 chr10:99078981-99078992 chr10:99078980-99078993 chr10:99078983-99078991 chr10:99078979-99078992 chr10:99078983-99078990 chr10:99078980-99078990 chr10:99078981-99078992 chr10:99078979-99078994
11	BACH1	chr10:99079941-99080973	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:99079458-99079625	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr10:99078543-99079108	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr10:99078448-99079053	A549	lung:	n/a	n/a
15	BHLHE40	chr10:99078576-99079167	HepG2	liver:	n/a	chr10:99079037-99079053 chr10:99079029-99079045
16	BHLHE40	chr10:99078722-99079085	A549	lung:	n/a	chr10:99079037-99079053 chr10:99079029-99079045
17	BHLHE40	chr10:99078551-99079202	GM12878	blood:	n/a	chr10:99079037-99079053 chr10:99079029-99079045
18	BHLHE40	chr10:99078525-99079243	K562	blood:	n/a	chr10:99079037-99079053 chr10:99079029-99079045
19	BRCA1	chr10:99078789-99079119	HepG2	liver:	n/a	n/a
20	BRCA1	chr10:99080002-99080308	HepG2	liver:	n/a	n/a
21	BRCA1	chr10:99078537-99079064	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr10:99078785-99079076	GM12878	blood:	n/a	n/a
23	BRCA1	chr10:99078572-99079163	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr10:99078411-99078861	K562	blood:	n/a	n/a
25	CCNT2	chr10:99078747-99080168	K562	blood:	n/a	chr10:99079089-99079098
26	CEBPB	chr10:99078641-99079157	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr10:99078867-99079080	HepG2	liver:	n/a	n/a
28	CEBPD	chr10:99078896-99079266	HepG2	liver:	n/a	n/a
29	CEBPD	chr10:99078934-99079209	HepG2	liver:	n/a	n/a
30	CHD1	chr10:99078484-99079167	GM12878	blood:	n/a	n/a
31	CHD1	chr10:99079774-99080144	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr10:99078487-99079148	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr10:99078311-99080203	IMR90	lung:	n/a	n/a
34	CHD2	chr10:99078720-99079059	HepG2	liver:	n/a	n/a
35	CHD2	chr10:99078528-99079144	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr10:99078735-99079246	K562	blood:	n/a	n/a
37	CHD2	chr10:99079891-99080006	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr10:99079872-99080230	HepG2	liver:	n/a	n/a
39	CHD2	chr10:99078500-99079324	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr10:99078481-99079241	ECC-1	luminal epithelium:	n/a	chr10:99078980-99078993
41	CREB1	chr10:99078472-99079224	HepG2	liver:	n/a	chr10:99078980-99078993
42	CREB1	chr10:99078541-99079228	H1-hESC	embryonic stem cell:	n/a	chr10:99078980-99078993
43	CREB1	chr10:99078479-99079249	K562	blood:	n/a	chr10:99078980-99078993
44	CREB1	chr10:99078439-99079378	HepG2	liver:	n/a	chr10:99078980-99078993
45	CREB1	chr10:99078518-99079238	GM12878	blood:	n/a	chr10:99078980-99078993
46	CREB1	chr10:99078752-99079131	A549	lung:	n/a	chr10:99078980-99078993
47	CREB1	chr10:99078542-99079200	ECC-1	luminal epithelium:	n/a	chr10:99078980-99078993
48	CREB1	chr10:99078602-99079249	K562	blood:	n/a	chr10:99078980-99078993
49	CREB1	chr10:99078437-99079395	A549	lung:	n/a	chr10:99078980-99078993
50	CREB1	chr10:99078438-99079236	H1-hESC	embryonic stem cell:	n/a	chr10:99078980-99078993

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:99079083-99079133	NT2-D1	testis:	n/a
2	chr10:99079083-99079133	HepG2	liver:	n/a
3	chr10:99079083-99079133	NT2-D1	testis:	n/a
4	chr10:99079083-99079133	HepG2	liver:	n/a
5	chr10:99080594-99080644	PFSK-1	brain:	n/a
6	chr10:99078818-99078868	ovcar-3	ovarian:	n/a
7	chr10:99078850-99078900	ovcar-3	ovarian:	n/a
8	chr10:99078818-99078868	NT2-D1	testis:	n/a
9	chr10:99078978-99079028	HRE	kidney:	n/a
10	chr10:99078818-99078868	HMEC	breast:	n/a
11	chr10:99078963-99079013	SKMC	muscle:	n/a
12	chr10:99078818-99078868	HEEpiC	esophagus:	n/a
13	chr10:99079074-99079124	NB4	blood:	n/a
14	chr10:99078978-99079028	MCF10A-Er-Src	breast:	n/a
15	chr10:99078702-99078752	HNPCEpiC	eye:	n/a
16	chr10:99078978-99079028	SK-N-MC	brain:	n/a
17	chr10:99078896-99078946	SK-N-SH_RA	brain:	n/a
18	chr10:99078965-99079015	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:99078850-99078900	HPAEpiC	pulmonary alveolar:	n/a
20	chr10:99078850-99078900	Caco-2	colon:	n/a
21	chr10:99078963-99079013	HEK293	kidney:	embryo
22	chr10:99078818-99078868	HCT-116	colon:	n/a
23	chr10:99078978-99079028	Hela-S3	cervix:	n/a
24	chr10:99078978-99079028	NH-A	brain:	n/a
25	chr10:99078824-99078874	ovcar-3	ovarian:	n/a
26	chr10:99078824-99078874	HRCEpiC	kidney:	n/a
27	chr10:99078978-99079028	CMK	blood:	n/a
28	chr10:99078812-99078862	PANC-1	pancreas:	n/a
29	chr10:99079798-99079848	PANC-1	pancreas:	n/a
30	chr10:99078818-99078868	HCF	heart:	n/a
31	chr10:99079074-99079124	SK-N-SH	brain:	n/a
32	chr10:99078812-99078862	HRCEpiC	kidney:	n/a
33	chr10:99078812-99078862	SAEC	small airway:	n/a
34	chr10:99078965-99079015	HepG2	liver:	n/a
35	chr10:99078896-99078946	A549	lung:	n/a
36	chr10:99078702-99078752	K562	blood:	n/a
37	chr10:99078824-99078874	AG04449	skin:	fetal
38	chr10:99080594-99080644	RPTEC	kidney:	n/a
39	chr10:99078963-99079013	ECC-1	luminal epithelium:	n/a
40	chr10:99078965-99079015	AG09319	gingival:	n/a
41	chr10:99078850-99078900	NHDF-neo	bronchial:	n/a
42	chr10:99078963-99079013	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:99078965-99079015	HRE	kidney:	n/a
44	chr10:99078978-99079028	SKMC	muscle:	n/a
45	chr10:99078818-99078868	MCF10A-Er-Src	breast:	n/a
46	chr10:99078978-99079028	NHBE	bronchial:	n/a
47	chr10:99078824-99078874	NHBE	bronchial:	n/a
48	chr10:99078702-99078752	Jurkat	blood:	n/a
49	chr10:99078702-99078752	SKMC	muscle:	n/a
50	chr10:99078812-99078862	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:99078212..99079127-chr2:113342181..113342990,2	Hela-S3	cervix:
2	chr10:99078612..99079288-chr16:20752504..20753231,2	Hela-S3	cervix:
3	chr10:99051582..99054067-chr10:99077169..99079188,3	K562	blood:
4	chr10:99066690..99071389-chr10:99076606..99080814,5	MCF-7	breast:
5	chr1:234746282..234747092-chr10:99078304..99078804,2	Hela-S3	cervix:
6	chr10:99051582..99055310-chr10:99077169..99083058,6	K562	blood:
7	chr10:99050343..99055587-chr10:99077475..99082102,7	MCF-7	breast:
8	chr10:99051058..99054984-chr10:99078319..99082092,7	MCF-7	breast:
9	chr10:99052064..99052648-chr10:99078773..99079491,2	NB4	blood:
10	chr10:99065771..99067454-chr10:99080586..99083013,2	MCF-7	breast:
11	chr1:145382532..145383482-chr10:99078590..99079115,2	Hela-S3	cervix:
12	chr10:99078866..99080436-chr17:56709012..56711151,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGAM1-4	chr10:99080498-99080991	NONHSAT015854

Variant related genes	Relation type
FRAT1	TF binding region
FRAT1	CpG island
ENSG00000066654	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000125611	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000237169	chromatin interactions
ENSG00000213390	chromatin interactions
ENSG00000269891	chromatin interactions

Extended variants
information (count: 98 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:98 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554437977	chr10:99078234-99078235	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs188328897	chr10:99078245-99078246	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs192174619	chr10:99078252-99078253	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs545528125	chr10:99078255-99078256	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs182864628	chr10:99078284-99078285	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs575738324	chr10:99078294-99078295	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs554346974	chr10:99078301-99078302	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs561585279	chr10:99078304-99078305	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs528648397	chr10:99078317-99078318	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs139371498	chr10:99078319-99078320	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs565514846	chr10:99078333-99078334	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs375573106	chr10:99078372-99078373	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs551478969	chr10:99078384-99078385	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs532768892	chr10:99078401-99078402	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs569279196	chr10:99078402-99078403	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs576573878	chr10:99078432-99078433	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs35717991	chr10:99078483-99078484	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548823126	chr10:99078507-99078508	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs567228385	chr10:99078539-99078540	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs534966483	chr10:99078611-99078612	Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs561688711	chr10:99078654-99078655	Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs566379170	chr10:99078699-99078700	Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs3740512	chr10:99078745-99078746	Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs368153998	chr10:99078801-99078802	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs113709542	chr10:99078849-99078850	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs538736522	chr10:99078854-99078855	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs374661155	chr10:99078894-99078895	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs557450545	chr10:99078924-99078925	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs3740513	chr10:99078931-99078932	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs3740514	chr10:99078954-99078955	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs150031197	chr10:99078963-99078964	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs573566565	chr10:99078976-99078977	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs540953576	chr10:99078979-99078980	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs565314745	chr10:99079013-99079014	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs11189127	chr10:99079023-99079024	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs544743643	chr10:99079027-99079028	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs373432834	chr10:99079035-99079036	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs145308736	chr10:99079061-99079062	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs530379830	chr10:99079067-99079068	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs548567967	chr10:99079075-99079076	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs566964311	chr10:99079190-99079191	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs7070246	chr10:99079255-99079256	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs201138590	chr10:99079276-99079277	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs370708476	chr10:99079297-99079298	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs571328245	chr10:99079389-99079390	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs112575281	chr10:99079394-99079395	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs3740516	chr10:99079404-99079405	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs538845227	chr10:99079407-99079408	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs113340568	chr10:99079430-99079431	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs557452732	chr10:99079455-99079456	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99074800-99078200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr10:99075600-99078400	Weak transcription	Lung	lung
3	chr10:99077000-99078200	Enhancers	Liver	Liver
4	chr10:99077200-99078200	Enhancers	Adipose Nuclei	Adipose
5	chr10:99077400-99078200	Enhancers	HepG2	liver
6	chr10:99077600-99078200	Enhancers	Primary T cells fromperipheralblood	blood
7	chr10:99077600-99078200	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr10:99077600-99078200	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr10:99077600-99078200	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr10:99077600-99078200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr10:99077600-99078200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr10:99077600-99078200	Enhancers	Placenta	Placenta
13	chr10:99077600-99078200	Enhancers	Fetal Thymus	thymus
14	chr10:99077600-99078400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr10:99077600-99078400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr10:99077600-99078400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr10:99077600-99079800	Active TSS	Fetal Intestine Large	intestine
18	chr10:99077600-99079800	Active TSS	Hela-S3	cervix
19	chr10:99077600-99080200	Active TSS	Brain Hippocampus Middle	brain
20	chr10:99077800-99078200	Enhancers	Primary B cells from peripheral blood	blood
21	chr10:99077800-99078200	Enhancers	Primary hematopoietic stem cells	blood
22	chr10:99077800-99078200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr10:99077800-99078200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr10:99077800-99078200	Enhancers	Brain Germinal Matrix	brain
25	chr10:99077800-99078400	Weak transcription	K562	blood
26	chr10:99077800-99080000	Active TSS	Primary T cells from cord blood	blood
27	chr10:99078000-99078200	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr10:99078000-99078200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr10:99078000-99078200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr10:99078000-99078200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr10:99078000-99078200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:99078000-99078200	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr10:99078000-99078200	Enhancers	Stomach Smooth Muscle	stomach
34	chr10:99078000-99078200	Enhancers	Dnd41	blood
35	chr10:99078000-99078800	Flanking Active TSS	Primary B cells from cord blood	blood
36	chr10:99078000-99079600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
37	chr10:99078000-99081200	Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr10:99078000-99081400	Active TSS	Monocytes-CD14+_RO01746	blood
39	chr10:99078200-99078400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr10:99078200-99078400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr10:99078200-99078400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr10:99078200-99078400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr10:99078200-99078400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr10:99078200-99078400	Active TSS	Liver	Liver
45	chr10:99078200-99078400	Active TSS	Brain Germinal Matrix	brain
46	chr10:99078200-99078400	Enhancers	Pancreas	Pancrea
47	chr10:99078200-99078400	Active TSS	HepG2	liver
48	chr10:99078200-99078600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
49	chr10:99078200-99078600	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr10:99078200-99078600	Flanking Active TSS	Primary T cells fromperipheralblood	blood

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