Variant report

Variant	esv1802456
Chromosome Location	chr10:94404824-94452430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:968)
CpG islands
(count:1407)
Chromatin interactive
region (count:33)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94448575-94448749	K562	blood:	n/a	n/a
2	ARID3A	chr10:94449623-94449834	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:94449642-94449923	K562	blood:	n/a	n/a
4	ARID3A	chr10:94422716-94422926	K562	blood:	n/a	n/a
5	ARID3A	chr10:94450472-94450789	K562	blood:	n/a	n/a
6	BACH1	chr10:94449756-94450595	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:94451457-94452071	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr10:94450119-94450426	GM12878	blood:	n/a	chr10:94450279-94450290
9	BHLHE40	chr10:94451821-94452123	HepG2	liver:	n/a	n/a
10	BHLHE40	chr10:94449290-94449318	K562	blood:	n/a	n/a
11	BHLHE40	chr10:94451790-94452225	K562	blood:	n/a	n/a
12	BHLHE40	chr10:94449745-94450830	K562	blood:	n/a	chr10:94450146-94450162
13	BHLHE40	chr10:94448577-94448982	K562	blood:	n/a	n/a
14	BHLHE40	chr10:94450084-94450434	GM12878	blood:	n/a	chr10:94450146-94450162
15	BHLHE40	chr10:94404882-94404994	A549	lung:	n/a	n/a
16	BHLHE40	chr10:94448540-94450445	HepG2	liver:	n/a	chr10:94449270-94449286 chr10:94450146-94450162 chr10:94449642-94449658
17	BRCA1	chr10:94450090-94450104	HepG2	liver:	n/a	n/a
18	BRCA1	chr10:94452113-94452119	HepG2	liver:	n/a	n/a
19	CBX3	chr10:94422559-94423000	K562	blood:	n/a	n/a
20	CBX3	chr10:94422636-94423056	HCT-116	colon:	n/a	n/a
21	CBX3	chr10:94445139-94445451	K562	blood:	n/a	n/a
22	CBX3	chr10:94448327-94449135	K562	blood:	n/a	n/a
23	CBX3	chr10:94422489-94423015	K562	blood:	n/a	n/a
24	CCNT2	chr10:94452213-94452432	K562	blood:	n/a	chr10:94452353-94452362
25	CCNT2	chr10:94448631-94451909	K562	blood:	n/a	chr10:94449521-94449530 chr10:94451255-94451264
26	CEBPB	chr10:94422603-94422900	K562	blood:	n/a	n/a
27	CEBPB	chr10:94440400-94440763	HepG2	liver:	n/a	n/a
28	CEBPB	chr10:94416810-94417148	Hela-S3	cervix:	n/a	chr10:94416963-94416974
29	CEBPB	chr10:94428693-94428805	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr10:94440455-94440734	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr10:94416795-94417153	HepG2	liver:	n/a	chr10:94416963-94416974
32	CEBPB	chr10:94440478-94440712	MCF-7	breast:	n/a	n/a
33	CEBPB	chr10:94416811-94417069	HepG2	liver:	n/a	chr10:94416963-94416974
34	CEBPB	chr10:94440506-94440654	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:94416861-94417074	MCF-7	breast:	n/a	chr10:94416963-94416974
36	CEBPB	chr10:94416859-94417057	K562	blood:	n/a	chr10:94416963-94416974
37	CEBPB	chr10:94428676-94428982	HepG2	liver:	n/a	chr10:94428810-94428821
38	CEBPB	chr10:94418750-94419130	HepG2	liver:	n/a	chr10:94418897-94418908
39	CEBPB	chr10:94450637-94450895	K562	blood:	n/a	n/a
40	CEBPB	chr10:94416739-94417100	HepG2	liver:	n/a	chr10:94416963-94416974
41	CEBPB	chr10:94416792-94417150	IMR90	lung:	n/a	chr10:94416963-94416974
42	CEBPB	chr10:94440405-94440764	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr10:94428690-94428986	A549	lung:	n/a	chr10:94428810-94428821
44	CEBPB	chr10:94416792-94417148	ECC-1	luminal epithelium:	n/a	chr10:94416963-94416974
45	CEBPB	chr10:94416819-94417133	A549	lung:	n/a	chr10:94416963-94416974
46	CEBPB	chr10:94416779-94417152	HepG2	liver:	n/a	chr10:94416963-94416974
47	CEBPB	chr10:94450237-94450353	HepG2	liver:	n/a	n/a
48	CEBPB	chr10:94440397-94440764	K562	blood:	n/a	n/a
49	CEBPB	chr10:94416790-94417202	A549	lung:	n/a	chr10:94416963-94416974
50	CEBPB	chr10:94416824-94417082	K562	blood:	n/a	chr10:94416963-94416974

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94452236-94452286	Jurkat	blood:	n/a
2	chr10:94451736-94451786	NHDF-neo	bronchial:	n/a
3	chr10:94450994-94451044	AG10803	skin:	n/a
4	chr10:94448728-94448778	HRE	kidney:	n/a
5	chr10:94452236-94452286	Jurkat	blood:	n/a
6	chr10:94451736-94451786	NHDF-neo	bronchial:	n/a
7	chr10:94450994-94451044	AG10803	skin:	n/a
8	chr10:94448728-94448778	HRE	kidney:	n/a
9	chr10:94451736-94451786	U87	brain:	n/a
10	chr10:94449250-94449300	HMEC	breast:	n/a
11	chr10:94429530-94429580	PFSK-1	brain:	n/a
12	chr10:94429569-94429619	GM12891	blood:	n/a
13	chr10:94449250-94449300	HEEpiC	esophagus:	n/a
14	chr10:94452311-94452361	GM12891	blood:	n/a
15	chr10:94450994-94451044	HNPCEpiC	eye:	n/a
16	chr10:94429569-94429619	ovcar-3	ovarian:	n/a
17	chr10:94449567-94449617	NHBE	bronchial:	n/a
18	chr10:94450056-94450106	LNCaP	prostate:	n/a
19	chr10:94429526-94429576	AG04450	lung:	fetal
20	chr10:94449567-94449617	HEEpiC	esophagus:	n/a
21	chr10:94448728-94448778	HMEC	breast:	n/a
22	chr10:94445035-94445085	HRE	kidney:	n/a
23	chr10:94449250-94449300	HCPEpiC	choroid plexus:	n/a
24	chr10:94429506-94429556	SK-N-MC	brain:	n/a
25	chr10:94448532-94448582	ProgFib	skin:	n/a
26	chr10:94451016-94451066	GM19239	blood:	n/a
27	chr10:94449567-94449617	Jurkat	blood:	n/a
28	chr10:94451736-94451786	PFSK-1	brain:	n/a
29	chr10:94450531-94450581	Hepatocyte	liver:	n/a
30	chr10:94449797-94449847	HCPEpiC	choroid plexus:	n/a
31	chr10:94448702-94448752	NB4	blood:	n/a
32	chr10:94452236-94452286	ECC-1	luminal epithelium:	n/a
33	chr10:94451518-94451568	HCT-116	colon:	n/a
34	chr10:94450994-94451044	GM19239	blood:	n/a
35	chr10:94451518-94451568	GM12892	blood:	n/a
36	chr10:94451625-94451675	NT2-D1	testis:	n/a
37	chr10:94451016-94451066	HNPCEpiC	eye:	n/a
38	chr10:94429530-94429580	MCF-7	breast:	n/a
39	chr10:94451625-94451675	LNCaP	prostate:	n/a
40	chr10:94450531-94450581	HepG2	liver:	n/a
41	chr10:94448728-94448778	MCF-7	breast:	n/a
42	chr10:94452236-94452286	BJ	skin:	n/a
43	chr10:94445035-94445085	SKMC	muscle:	n/a
44	chr10:94450866-94450916	MCF10A-Er-Src	breast:	n/a
45	chr10:94429542-94429592	HRPEpiC	eye:	n/a
46	chr10:94451736-94451786	BJ	skin:	n/a
47	chr10:94429542-94429592	MCF10A-Er-Src	breast:	n/a
48	chr10:94450994-94451044	HUVEC	blood vessel:	n/a
49	chr10:94429506-94429556	HAEpiC	amniotic membrane:	n/a
50	chr10:94448702-94448752	HCPEpiC	choroid plexus:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94333616..94336720-chr10:94448718..94451044,3	K562	blood:
2	chr10:94415353..94417803-chr10:94419120..94421104,2	K562	blood:
3	chr10:94349533..94354628-chr10:94448059..94453493,12	K562	blood:
4	chr10:94415353..94417803-chr10:94419120..94421104,2	K562	blood:
5	chr10:94408475..94411448-chr10:94454025..94455540,2	K562	blood:
6	chr10:94449758..94450309-chr20:30192485..30193219,2	Hela-S3	cervix:
7	chr10:94332371..94335153-chr10:94446165..94448467,2	K562	blood:
8	chr10:94448193..94452899-chr10:94604769..94609293,6	K562	blood:
9	chr10:94349914..94352600-chr10:94405962..94408732,2	MCF-7	breast:
10	chr10:94353767..94355428-chr10:94415113..94417602,2	MCF-7	breast:
11	chr10:94403550..94405303-chr10:94448341..94451102,2	K562	blood:
12	chr10:94449314..94450224-chr16:30388710..30389229,2	NB4	blood:
13	chr10:94449913..94450519-chr18:12990641..12991585,2	Hela-S3	cervix:
14	chr10:94439547..94442442-chr10:94446922..94448732,2	MCF-7	breast:
15	chr10:94437792..94440441-chr10:94441307..94443434,2	K562	blood:
16	chr10:94434850..94438940-chr10:94446699..94450647,3	K562	blood:
17	chr10:94407828..94410112-chr10:94420940..94422860,2	K562	blood:
18	chr10:94449678..94450357-chr11:62359130..62359860,2	Hela-S3	cervix:
19	chr10:94349533..94356622-chr10:94447410..94453498,11	K562	blood:
20	chr10:94449237..94450232-chr6:27805942..27806496,2	NB4	blood:
21	chr10:94434338..94436350-chr10:94446810..94449570,2	K562	blood:
22	chr10:94449475..94450112-chr19:14529907..14530785,2	Hela-S3	cervix:
23	chr10:94439735..94442066-chr10:94601811..94604673,2	K562	blood:
24	chr10:94450024..94450724-chr19:12901932..12902636,2	Hela-S3	cervix:
25	chr10:94334145..94336156-chr10:94441112..94444728,3	K562	blood:
26	chr10:94449603..94452740-chr10:94589464..94592452,3	K562	blood:
27	chr10:94351775..94355250-chr10:94403169..94406867,3	K562	blood:
28	chr10:94437792..94440441-chr10:94441307..94443434,2	K562	blood:
29	chr10:94441256..94444670-chr10:94449156..94451252,3	MCF-7	breast:
30	chr10:94430325..94433160-chr10:94453394..94455547,2	K562	blood:
31	chr10:94407828..94410112-chr10:94420940..94422860,2	K562	blood:
32	chr10:94440739..94442413-chr10:94446603..94449404,2	K562	blood:
33	chr10:94449635..94450319-chr15:59396946..59397778,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HHEX-2	chr10:94440441-94440641	expReg_chr10_6166_+
2	lnc-KIF11-2	chr10:94418801-94419055	NONHSAT015671
3	lnc-HHEX-1	chr10:94440775-94440994	expReg_chr10_6169_+

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KIF11	hsa-miR-340-5p	chr10:94414109-94414130
2	KIF11	hsa-miR-186-5p	chr10:94414077-94414099
3	KIF11	hsa-miR-186-5p	chr10:94414695-94414716
4	KIF11	hsa-miR-30a-5p	chr10:94414702-94414723

Variant related genes	Relation type
RN7SL644P	TF binding region
EIF2S2P3	TF binding region
HHEX	TF binding region
RN7SL644P	CpG island
EIF2S2P3	CpG island
HHEX	CpG island
ENSG00000149016	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000171223	chromatin interactions
ENSG00000152804	chromatin interactions
ENSG00000157456	chromatin interactions
ENSG00000138190	chromatin interactions
ENSG00000119912	chromatin interactions
ENSG00000266969	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000138160	chromatin interactions
ENSG00000123136	chromatin interactions
ENSG00000101639	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000184348	chromatin interactions

Extended variants
information (count: 1565 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7917359	chr10:94404824-94404825	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77719947	chr10:94404827-94404828	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs76357416	chr10:94404832-94404833	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs554505538	chr10:94404847-94404848	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs557168039	chr10:94404943-94404944	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs193147939	chr10:94404949-94404950	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528894837	chr10:94404983-94404984	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544168189	chr10:94405040-94405041	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs563969992	chr10:94405108-94405109	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs202150514	chr10:94405168-94405169	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548968453	chr10:94405194-94405195	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs201096319	chr10:94405224-94405225	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577542856	chr10:94405243-94405244	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs146826402	chr10:94405264-94405265	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369316954	chr10:94405267-94405268	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs565781291	chr10:94405273-94405274	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs36070037	chr10:94405344-94405345	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34647366	chr10:94405364-94405365	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs199882892	chr10:94405421-94405422	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs199633318	chr10:94405425-94405426	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562149720	chr10:94405450-94405451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184428907	chr10:94405464-94405465	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534661435	chr10:94405472-94405473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368886313	chr10:94405512-94405513	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549689915	chr10:94405553-94405554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs569596527	chr10:94405610-94405611	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538463723	chr10:94405647-94405648	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145476079	chr10:94405648-94405649	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79635445	chr10:94405701-94405702	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534674250	chr10:94405703-94405704	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370095733	chr10:94405708-94405709	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs33915127	chr10:94405726-94405727	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs370644565	chr10:94405739-94405740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554359332	chr10:94405748-94405749	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs186375170	chr10:94405768-94405769	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs375123979	chr10:94405771-94405772	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537231083	chr10:94405811-94405812	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189190455	chr10:94405825-94405826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369641571	chr10:94405826-94405827	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs577583875	chr10:94405883-94405884	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557010816	chr10:94405884-94405885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546421624	chr10:94405955-94405956	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181165490	chr10:94405961-94405962	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573344940	chr10:94405983-94405984	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542353447	chr10:94406004-94406005	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541844839	chr10:94406007-94406008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371598033	chr10:94406039-94406040	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530845326	chr10:94406126-94406127	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550528383	chr10:94406128-94406129	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs544008135	chr10:94406213-94406214	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	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
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94354000-94420000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:94354200-94416000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr10:94363600-94410200	Weak transcription	Fetal Kidney	kidney
4	chr10:94364000-94416400	Strong transcription	Dnd41	blood
5	chr10:94364200-94417400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr10:94364400-94415200	Weak transcription	Fetal Heart	heart
7	chr10:94365600-94415600	Strong transcription	Fetal Thymus	thymus
8	chr10:94366000-94409600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr10:94367200-94411400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr10:94371000-94408600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr10:94371000-94414600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr10:94371000-94417000	Weak transcription	Primary B cells from cord blood	blood
13	chr10:94371800-94408800	Weak transcription	Fetal Brain Female	brain
14	chr10:94374800-94410400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr10:94374800-94416000	Weak transcription	Placenta	Placenta
16	chr10:94374800-94418600	Weak transcription	Brain Germinal Matrix	brain
17	chr10:94383000-94414600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr10:94384000-94414200	Weak transcription	Primary T cells from cord blood	blood
19	chr10:94384000-94416400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr10:94389000-94416400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr10:94391400-94415000	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr10:94391400-94415400	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr10:94391400-94415400	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr10:94391400-94415400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr10:94391400-94415400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr10:94391400-94415800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr10:94392000-94415400	Weak transcription	Small Intestine	intestine
28	chr10:94392400-94406600	Weak transcription	NH-A	brain
29	chr10:94395000-94414800	Weak transcription	Fetal Brain Male	brain
30	chr10:94395400-94411400	Weak transcription	Fetal Intestine Large	intestine
31	chr10:94396200-94412200	Weak transcription	Fetal Muscle Leg	muscle
32	chr10:94396400-94412600	Weak transcription	Liver	Liver
33	chr10:94396400-94418200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr10:94398400-94421200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr10:94399000-94407200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr10:94399400-94410600	Weak transcription	Fetal Stomach	stomach
37	chr10:94400000-94406600	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr10:94400200-94405000	Weak transcription	Osteobl	bone
39	chr10:94400200-94416800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr10:94400800-94407200	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr10:94400800-94410800	Weak transcription	Fetal Intestine Small	intestine
42	chr10:94400800-94411000	Weak transcription	Thymus	Thymus
43	chr10:94401000-94406000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr10:94401200-94409600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr10:94402200-94406200	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr10:94402200-94407000	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr10:94402400-94407000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr10:94402400-94407000	Weak transcription	Fetal Lung	lung
49	chr10:94402600-94406200	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr10:94403600-94405200	Strong transcription	Fetal Muscle Trunk	muscle

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