Variant report

Variant	nsv895913
Chromosome Location	chr10:98854410-98884402
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	BHLHE40	chr10:98856148-98856722	GM12878	blood:	n/a	n/a
2	CEBPB	chr10:98874703-98874955	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr10:98874707-98874986	IMR90	lung:	n/a	n/a
4	CEBPB	chr10:98874738-98874996	K562	blood:	n/a	n/a
5	CEBPB	chr10:98874699-98874951	HepG2	liver:	n/a	n/a
6	CEBPB	chr10:98874737-98875016	A549	lung:	n/a	n/a
7	CEBPB	chr10:98880950-98881156	A549	lung:	n/a	chr10:98881004-98881015 chr10:98881004-98881013
8	CEBPB	chr10:98880930-98881106	HepG2	liver:	n/a	chr10:98881004-98881015 chr10:98881004-98881013
9	CHD2	chr10:98856842-98856987	GM12878	blood:	n/a	n/a
10	CHD2	chr10:98856333-98856587	GM12878	blood:	n/a	n/a
11	CTCF	chr10:98877200-98877350	HMEC	breast:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
12	CTCF	chr10:98877240-98877390	K562	blood:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
13	CTCF	chr10:98877240-98877390	HepG2	liver:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
14	CTCF	chr10:98877260-98877410	GM12865	blood:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
15	CTCF	chr10:98861200-98861350	GM12878	blood:	n/a	n/a
16	CTCF	chr10:98877220-98877370	AoAF	blood vessel:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
17	CTCF	chr10:98877320-98877470	GM12864	blood:	n/a	chr10:98877323-98877336 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
18	CTCF	chr10:98861260-98861410	GM12865	blood:	n/a	n/a
19	CTCF	chr10:98877180-98877330	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr10:98861140-98861290	K562	blood:	n/a	n/a
21	CTCF	chr10:98881780-98881930	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr10:98877280-98877430	HUVEC	blood vessel:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
23	CTCF	chr10:98877240-98877390	NHEK	skin:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
24	CTCF	chr10:98877200-98877350	GM06990	blood:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
25	CTCF	chr10:98861096-98861165	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr10:98877240-98877390	HEEpiC	esophagus:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
27	CTCF	chr10:98877240-98877390	HCPEpiC	choroid plexus:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
28	CTCF	chr10:98877160-98877310	GM12872	blood:	n/a	n/a
29	CTCF	chr10:98861080-98861230	GM12869	blood:	n/a	n/a
30	CTCF	chr10:98861040-98861190	HAc	cerebellar:	n/a	n/a
31	CTCF	chr10:98877138-98877511	GM12878	blood:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
32	CTCF	chr10:98877076-98877567	A549	lung:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
33	CTCF	chr10:98877151-98877594	MCF-7	breast:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
34	CTCF	chr10:98860920-98861070	A549	lung:	n/a	n/a
35	CTCF	chr10:98877260-98877410	AG04449	skin:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
36	CTCF	chr10:98877280-98877430	HFF-Myc	foreskin:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
37	CTCF	chr10:98877260-98877410	Hela-S3	cervix:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
38	CTCF	chr10:98877252-98877424	GM13977	blood:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
39	CTCF	chr10:98861460-98861610	GM12870	blood:	n/a	n/a
40	CTCF	chr10:98861120-98861270	BE2_C	brain:	n/a	n/a
41	CTCF	chr10:98861146-98861217	HepG2	liver:	n/a	n/a
42	CTCF	chr10:98877208-98877468	H1-hESC	embryonic stem cell:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
43	CTCF	chr10:98877260-98877410	Caco-2	colon:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
44	CTCF	chr10:98877165-98877456	T-47D	breast:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
45	CTCF	chr10:98877213-98877438	GM12878	blood:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
46	CTCF	chr10:98877240-98877390	GM12869	blood:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
47	CTCF	chr10:98877220-98877370	HMF	breast:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
48	CTCF	chr10:98877280-98877430	GM12864	blood:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
49	CTCF	chr10:98877214-98877429	A549	lung:	n/a	chr10:98877323-98877336 chr10:98877316-98877337 chr10:98877325-98877346 chr10:98877324-98877334 chr10:98877321-98877339 chr10:98877323-98877341
50	CTCF	chr10:98862260-98862410	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:98862384-98862434	GM06990	blood:	n/a
2	chr10:98862320-98862370	BE2_C	brain:	n/a
3	chr10:98855762-98855812	HCT-116	colon:	n/a
4	chr10:98861318-98861368	GM12892	blood:	n/a
5	chr10:98862320-98862370	HEEpiC	esophagus:	n/a
6	chr10:98861029-98861079	Jurkat	blood:	n/a
7	chr10:98861029-98861079	CMK	blood:	n/a
8	chr10:98862320-98862370	GM12891	blood:	n/a
9	chr10:98861029-98861079	GM12891	blood:	n/a
10	chr10:98862320-98862370	PANC-1	pancreas:	n/a
11	chr10:98862384-98862434	GM12892	blood:	n/a
12	chr10:98862384-98862434	SK-N-SH_RA	brain:	n/a
13	chr10:98855762-98855812	HUVEC	blood vessel:	n/a
14	chr10:98861029-98861079	U87	brain:	n/a
15	chr10:98861318-98861368	BJ	skin:	n/a
16	chr10:98861318-98861368	HCPEpiC	choroid plexus:	n/a
17	chr10:98862320-98862370	SK-N-SH	brain:	n/a
18	chr10:98861318-98861368	HCM	heart:	n/a
19	chr10:98862384-98862434	AG10803	skin:	n/a
20	chr10:98862320-98862370	HIPEpiC	eye:	n/a
21	chr10:98862320-98862370	GM12892	blood:	n/a
22	chr10:98862384-98862434	HCPEpiC	choroid plexus:	n/a
23	chr10:98855762-98855812	A549	lung:	n/a
24	chr10:98861318-98861368	SAEC	small airway:	n/a
25	chr10:98861029-98861079	BJ	skin:	n/a
26	chr10:98855762-98855812	HNPCEpiC	eye:	n/a
27	chr10:98862384-98862434	GM12891	blood:	n/a
28	chr10:98862320-98862370	HRPEpiC	eye:	n/a
29	chr10:98862320-98862370	HCM	heart:	n/a
30	chr10:98862320-98862370	RPTEC	kidney:	n/a
31	chr10:98862320-98862370	NHDF-neo	bronchial:	n/a
32	chr10:98862384-98862434	PrEC	prostate:	n/a
33	chr10:98862384-98862434	IMR90	lung:	fetal
34	chr10:98861029-98861079	SKMC	muscle:	n/a
35	chr10:98861318-98861368	IMR90	lung:	fetal
36	chr10:98861318-98861368	HPAEpiC	pulmonary alveolar:	n/a
37	chr10:98862384-98862434	ovcar-3	ovarian:	n/a
38	chr10:98861318-98861368	PANC-1	pancreas:	n/a
39	chr10:98861318-98861368	GM19239	blood:	n/a
40	chr10:98861029-98861079	HMEC	breast:	n/a
41	chr10:98862320-98862370	HCF	heart:	n/a
42	chr10:98862384-98862434	SK-N-SH	brain:	n/a
43	chr10:98862320-98862370	HRE	kidney:	n/a
44	chr10:98861029-98861079	HEK293	kidney:	embryo
45	chr10:98855762-98855812	HCF	heart:	n/a
46	chr10:98862320-98862370	U87	brain:	n/a
47	chr10:98861318-98861368	MCF10A-Er-Src	breast:	n/a
48	chr10:98855762-98855812	CMK	blood:	n/a
49	chr10:98861029-98861079	AoSMC	blood vessel:	n/a
50	chr10:98862320-98862370	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:98841106..98841891-chr10:98876867..98877472,3	MCF-7	breast:
2	chr10:98877113..98877837-chr10:98970293..98970909,2	MCF-7	breast:
3	chr10:98874182..98876788-chr10:98880678..98883082,2	K562	blood:
4	chr10:98875421..98877829-chr10:98897126..98899763,2	K562	blood:
5	chr10:98876065..98877734-chr10:98879477..98883103,3	K562	blood:
6	chr10:98853765..98854488-chr10:98874921..98875685,2	MCF-7	breast:
7	chr10:98858093..98860956-chr10:98957219..98958927,2	K562	blood:
8	chr10:98876065..98877734-chr10:98879477..98883103,3	K562	blood:
9	chr10:98832792..98833549-chr10:98877399..98877991,2	K562	blood:
10	chr10:98841171..98842122-chr10:98876891..98877589,2	MCF-7	breast:
11	chr10:98876999..98877834-chr10:98994252..98994779,2	MCF-7	breast:
12	chr10:98865480..98867358-chr10:98868311..98871144,2	MCF-7	breast:
13	chr10:98869547..98870254-chr10:98969992..98970708,2	MCF-7	breast:
14	chr10:98882941..98884607-chr10:98892301..98894138,2	K562	blood:
15	chr10:98841269..98842045-chr10:98860672..98861381,3	MCF-7	breast:
16	chr10:98796702..98797781-chr10:98876858..98877776,6	MCF-7	breast:
17	chr10:98880505..98883448-chr10:98886169..98887712,2	MCF-7	breast:
18	chr10:98857228..98859205-chr10:98862537..98865194,2	MCF-7	breast:
19	chr10:98853765..98854488-chr10:98874921..98875685,2	MCF-7	breast:
20	chr10:98859426..98860138-chr10:98970400..98970959,2	K562	blood:
21	chr10:98852925..98854951-chr10:98856338..98858099,2	K562	blood:
22	chr10:98832441..98833621-chr10:98876782..98877820,10	MCF-7	breast:
23	chr10:98857228..98859205-chr10:98862537..98865194,2	MCF-7	breast:
24	chr10:98797214..98797746-chr10:98876875..98877694,2	K562	blood:
25	chr10:98858173..98860221-chr10:98861686..98864026,3	K562	blood:
26	chr10:98852925..98854951-chr10:98856338..98858099,2	K562	blood:
27	chr10:98874182..98876788-chr10:98880678..98883082,2	K562	blood:
28	chr10:98865480..98867358-chr10:98868311..98871144,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf12-2	chr10:98862512-98862867	NONHSAT015847
2	lnc-C10orf12-2	chr10:98862513-98862867	ENSG00000234855.1
3	lnc-FRAT2-4	chr10:98861788-98861841	NONHSAT015846
4	lnc-FRAT2-4	chr10:98861108-98861198	NONHSAT015846
5	lnc-FRAT2-4	chr10:98862276-98862313	NONHSAT015846
6	lnc-C10orf12-2	chr10:98863077-98863248	NONHSAT015847
7	lnc-C10orf12-2	chr10:98863343-98863677	NONHSAT015847
8	lnc-C10orf12-2	chr10:98863077-98863248	ENSG00000234855.1
9	lnc-C10orf12-2	chr10:98863343-98863504	ENSG00000234855.1
10	lnc-FRAT2-4	chr10:98862053-98862150	NONHSAT015846

Variant related genes	Relation type
SLIT1	TF binding region
ENSG00000234855	TF binding region
SLIT1	CpG island
ENSG00000234855	CpG island
ENSG00000234855	chromatin interactions
ENSG00000187122	chromatin interactions

Extended variants
information (count: 1120 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1120 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2861828	chr10:98854410-98854411	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191218823	chr10:98854433-98854434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535647833	chr10:98854440-98854441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7922048	chr10:98854447-98854448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113449530	chr10:98854454-98854455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536756780	chr10:98854468-98854469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113931451	chr10:98854490-98854491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572365257	chr10:98854509-98854510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573391299	chr10:98854525-98854526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112154245	chr10:98854533-98854534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192539854	chr10:98854620-98854621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142469148	chr10:98854651-98854652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs902471	chr10:98854678-98854679	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs377112667	chr10:98854692-98854693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7922231	chr10:98854714-98854715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2861829	chr10:98854783-98854784	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs560646436	chr10:98854812-98854813	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs528327138	chr10:98854868-98854869	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs546460779	chr10:98854869-98854870	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs571543802	chr10:98854884-98854885	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs112425934	chr10:98854886-98854887	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs538575267	chr10:98854891-98854892	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs367783140	chr10:98854896-98854897	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs550856116	chr10:98854929-98854930	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs35064006	chr10:98854934-98854935	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs536605515	chr10:98854973-98854974	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs560944727	chr10:98854976-98854977	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs140513096	chr10:98855032-98855033	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs529403109	chr10:98855045-98855046	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs548861651	chr10:98855048-98855049	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs554606722	chr10:98855056-98855057	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs145636496	chr10:98855074-98855075	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs558863007	chr10:98855085-98855086	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs577340221	chr10:98855087-98855088	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs544520376	chr10:98855089-98855090	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs146588979	chr10:98855107-98855108	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs140980664	chr10:98855150-98855151	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs189855977	chr10:98855212-98855213	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs181990010	chr10:98855259-98855260	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs150147365	chr10:98855307-98855308	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs540293456	chr10:98855309-98855310	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs372538843	chr10:98855315-98855316	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs564945304	chr10:98855358-98855359	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs533688703	chr10:98855381-98855382	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs550900750	chr10:98855387-98855388	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs569172813	chr10:98855444-98855445	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs201415709	chr10:98855460-98855461	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs369027182	chr10:98855461-98855462	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs530159530	chr10:98855464-98855465	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs17112401	chr10:98855465-98855466	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98841200-98869200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:98847400-98855200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr10:98847400-98860600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr10:98847600-98855400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr10:98848200-98856400	Weak transcription	Thymus	Thymus
6	chr10:98848800-98855000	Weak transcription	Brain Germinal Matrix	brain
7	chr10:98849000-98855600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:98850000-98855200	Weak transcription	Brain Anterior Caudate	brain
9	chr10:98850000-98855400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr10:98850000-98855400	Weak transcription	Right Atrium	heart
11	chr10:98853200-98858200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr10:98853800-98855000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr10:98854000-98855600	Weak transcription	Ovary	ovary
14	chr10:98854200-98855800	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr10:98854200-98859400	Enhancers	Fetal Heart	heart
16	chr10:98854400-98856600	Enhancers	Fetal Thymus	thymus
17	chr10:98854800-98855800	Enhancers	Primary T cells fromperipheralblood	blood
18	chr10:98854800-98856000	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr10:98854800-98856200	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr10:98854800-98857000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr10:98855000-98855200	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr10:98855000-98855600	Enhancers	Brain Germinal Matrix	brain
23	chr10:98855000-98857400	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr10:98855000-98858400	Enhancers	Fetal Brain Male	brain
25	chr10:98855000-98858600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr10:98855200-98855600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr10:98855200-98855800	Enhancers	Brain Cingulate Gyrus	brain
28	chr10:98855200-98856000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr10:98855200-98856000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr10:98855200-98856000	Enhancers	Left Ventricle	heart
31	chr10:98855200-98856200	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr10:98855200-98856200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr10:98855200-98857000	Bivalent Enhancer	Dnd41	blood
34	chr10:98855200-98857200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:98855200-98857200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr10:98855200-98857400	Enhancers	Brain Anterior Caudate	brain
37	chr10:98855200-98858800	Enhancers	Right Ventricle	heart
38	chr10:98855400-98855600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:98855400-98855600	Bivalent Enhancer	Fetal Intestine Small	intestine
40	chr10:98855400-98855600	Enhancers	Fetal Kidney	kidney
41	chr10:98855400-98855600	Bivalent Enhancer	GM12878-XiMat	blood
42	chr10:98855400-98855800	Enhancers	Gastric	stomach
43	chr10:98855400-98855800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
44	chr10:98855400-98856000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr10:98855400-98856000	Enhancers	Spleen	Spleen
46	chr10:98855400-98856200	Enhancers	H1 Cell Line	embryonic stem cell
47	chr10:98855400-98856200	Bivalent Enhancer	Adipose Nuclei	Adipose
48	chr10:98855400-98856200	Enhancers	Fetal Brain Female	brain
49	chr10:98855400-98857000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:98855400-98857000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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