Variant report

Variant	esv3493295
Chromosome Location	chr10:94448772-94450870
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:577)
CpG islands
(count:427)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94450472-94450789	K562	blood:	n/a	n/a
2	ARID3A	chr10:94449642-94449923	K562	blood:	n/a	n/a
3	ARID3A	chr10:94449623-94449834	HepG2	liver:	n/a	n/a
4	BACH1	chr10:94449756-94450595	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr10:94450119-94450426	GM12878	blood:	n/a	chr10:94450279-94450290
6	BHLHE40	chr10:94449290-94449318	K562	blood:	n/a	n/a
7	BHLHE40	chr10:94449745-94450830	K562	blood:	n/a	chr10:94450146-94450162
8	BHLHE40	chr10:94450084-94450434	GM12878	blood:	n/a	chr10:94450146-94450162
9	BHLHE40	chr10:94448577-94448982	K562	blood:	n/a	n/a
10	BHLHE40	chr10:94448540-94450445	HepG2	liver:	n/a	chr10:94449270-94449286 chr10:94450146-94450162 chr10:94449642-94449658
11	BRCA1	chr10:94450090-94450104	HepG2	liver:	n/a	n/a
12	CBX3	chr10:94448327-94449135	K562	blood:	n/a	n/a
13	CCNT2	chr10:94448631-94451909	K562	blood:	n/a	chr10:94449521-94449530 chr10:94451255-94451264
14	CEBPB	chr10:94450637-94450895	K562	blood:	n/a	n/a
15	CEBPB	chr10:94450237-94450353	HepG2	liver:	n/a	n/a
16	CEBPB	chr10:94450133-94450542	Hela-S3	cervix:	n/a	n/a
17	CEBPD	chr10:94449523-94449905	HepG2	liver:	n/a	n/a
18	CEBPD	chr10:94450441-94450915	K562	blood:	n/a	n/a
19	CEBPD	chr10:94450371-94450938	K562	blood:	n/a	n/a
20	CEBPD	chr10:94449571-94450015	HepG2	liver:	n/a	n/a
21	CEBPD	chr10:94449168-94449517	HepG2	liver:	n/a	n/a
22	CHD1	chr10:94450625-94451087	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr10:94449342-94449343	K562	blood:	n/a	n/a
24	CHD2	chr10:94450553-94450647	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr10:94448750-94448936	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr10:94449248-94450546	Hela-S3	cervix:	n/a	chr10:94449522-94449532 chr10:94449385-94449395
27	CREB1	chr10:94449053-94450362	A549	lung:	n/a	n/a
28	CTBP2	chr10:94449746-94452477	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTBP2	chr10:94448629-94449382	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr10:94450180-94450330	AG04449	skin:	n/a	n/a
31	CTCF	chr10:94449900-94450050	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr10:94448660-94448810	GM12873	blood:	n/a	n/a
33	CTCF	chr10:94448720-94448870	BJ	skin:	n/a	n/a
34	CTCF	chr10:94448700-94448850	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr10:94450060-94450210	Hela-S3	cervix:	n/a	chr10:94450145-94450158 chr10:94450142-94450160
36	CTCF	chr10:94449320-94449470	GM12873	blood:	n/a	n/a
37	CTCF	chr10:94449800-94449950	GM12865	blood:	n/a	n/a
38	CTCF	chr10:94448888-94449046	GM19240	blood:	n/a	n/a
39	CTCF	chr10:94448700-94448850	HPF	lung:	n/a	n/a
40	CTCF	chr10:94450100-94450250	GM12866	blood:	n/a	chr10:94450145-94450158 chr10:94450142-94450160
41	CTCF	chr10:94449920-94450070	BJ	skin:	n/a	n/a
42	CTCF	chr10:94448800-94448950	HVMF	connective:	n/a	n/a
43	CTCF	chr10:94448680-94448830	GM12874	blood:	n/a	n/a
44	CTCF	chr10:94448840-94448990	WI-38	lung:	n/a	n/a
45	CTCF	chr10:94448640-94448790	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr10:94448640-94448790	HCM	heart:	n/a	n/a
47	CTCF	chr10:94448820-94448970	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr10:94448700-94448850	AG09309	skin:	n/a	n/a
49	CTCF	chr10:94448840-94448990	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr10:94449937-94449948	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94449567-94449617	HRPEpiC	eye:	n/a
2	chr10:94448728-94448778	AG04449	skin:	fetal
3	chr10:94449797-94449847	Jurkat	blood:	n/a
4	chr10:94449567-94449617	HEK293	kidney:	embryo
5	chr10:94449250-94449300	NH-A	brain:	n/a
6	chr10:94450531-94450581	PANC-1	pancreas:	n/a
7	chr10:94449797-94449847	SK-N-SH	brain:	n/a
8	chr10:94450056-94450106	AG04450	lung:	fetal
9	chr10:94450056-94450106	HUVEC	blood vessel:	n/a
10	chr10:94450056-94450106	SKMC	muscle:	n/a
11	chr10:94449797-94449847	HUVEC	blood vessel:	n/a
12	chr10:94450056-94450106	NT2-D1	testis:	n/a
13	chr10:94449250-94449300	NHBE	bronchial:	n/a
14	chr10:94450056-94450106	SK-N-SH_RA	brain:	n/a
15	chr10:94449797-94449847	HCT-116	colon:	n/a
16	chr10:94449567-94449617	AG09319	gingival:	n/a
17	chr10:94448728-94448778	HIPEpiC	eye:	n/a
18	chr10:94450056-94450106	NH-A	brain:	n/a
19	chr10:94450531-94450581	HRE	kidney:	n/a
20	chr10:94449797-94449847	HPAEpiC	pulmonary alveolar:	n/a
21	chr10:94450531-94450581	NT2-D1	testis:	n/a
22	chr10:94449797-94449847	H1-hESC	embryonic stem cell:	embryo
23	chr10:94448728-94448778	SK-N-SH	brain:	n/a
24	chr10:94450866-94450916	HepG2	liver:	n/a
25	chr10:94449567-94449617	Jurkat	blood:	n/a
26	chr10:94449797-94449847	HRPEpiC	eye:	n/a
27	chr10:94449250-94449300	AG09319	gingival:	n/a
28	chr10:94449797-94449847	CMK	blood:	n/a
29	chr10:94448728-94448778	HEK293	kidney:	embryo
30	chr10:94450531-94450581	ProgFib	skin:	n/a
31	chr10:94448728-94448778	GM06990	blood:	n/a
32	chr10:94449250-94449300	Hepatocyte	liver:	n/a
33	chr10:94450866-94450916	K562	blood:	n/a
34	chr10:94450866-94450916	BJ	skin:	n/a
35	chr10:94449797-94449847	ECC-1	luminal epithelium:	n/a
36	chr10:94450056-94450106	AG10803	skin:	n/a
37	chr10:94449797-94449847	AoSMC	blood vessel:	n/a
38	chr10:94449797-94449847	HEEpiC	esophagus:	n/a
39	chr10:94449250-94449300	AG09309	skin:	n/a
40	chr10:94449567-94449617	PrEC	prostate:	n/a
41	chr10:94449797-94449847	K562	blood:	n/a
42	chr10:94449797-94449847	AG04449	skin:	fetal
43	chr10:94449567-94449617	LNCaP	prostate:	n/a
44	chr10:94449567-94449617	HIPEpiC	eye:	n/a
45	chr10:94450866-94450916	HNPCEpiC	eye:	n/a
46	chr10:94450056-94450106	ovcar-3	ovarian:	n/a
47	chr10:94449250-94449300	BE2_C	brain:	n/a
48	chr10:94450531-94450581	AG10803	skin:	n/a
49	chr10:94449797-94449847	HepG2	liver:	n/a
50	chr10:94449567-94449617	SAEC	small airway:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94349533..94354628-chr10:94448059..94453493,12	K562	blood:
2	chr10:94349533..94356622-chr10:94447410..94453498,11	K562	blood:
3	chr10:94448193..94452899-chr10:94604769..94609293,6	K562	blood:
4	chr10:94449678..94450357-chr11:62359130..62359860,2	Hela-S3	cervix:
5	chr10:94449913..94450519-chr18:12990641..12991585,2	Hela-S3	cervix:
6	chr10:94333616..94336720-chr10:94448718..94451044,3	K562	blood:
7	chr10:94449635..94450319-chr15:59396946..59397778,2	NB4	blood:
8	chr10:94449603..94452740-chr10:94589464..94592452,3	K562	blood:
9	chr10:94450024..94450724-chr19:12901932..12902636,2	Hela-S3	cervix:
10	chr10:94449758..94450309-chr20:30192485..30193219,2	Hela-S3	cervix:
11	chr10:94449475..94450112-chr19:14529907..14530785,2	Hela-S3	cervix:
12	chr10:94449314..94450224-chr16:30388710..30389229,2	NB4	blood:
13	chr10:94449237..94450232-chr6:27805942..27806496,2	NB4	blood:

No data

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

Extended variants
information (count: 90 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149759733	chr10:94448774-94448775	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs76425330	chr10:94448793-94448794	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs573117244	chr10:94448802-94448803	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs556522395	chr10:94448806-94448807	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs542053391	chr10:94448816-94448817	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs117739875	chr10:94448838-94448839	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs562305227	chr10:94448847-94448848	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs113555157	chr10:94448851-94448852	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs544652387	chr10:94448855-94448856	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs564324947	chr10:94448867-94448868	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs533335614	chr10:94448875-94448876	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs552512817	chr10:94448890-94448891	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs34593856	chr10:94448895-94448896	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs559715342	chr10:94448897-94448898	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs528370402	chr10:94448898-94448899	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs181829459	chr10:94448920-94448921	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs548134764	chr10:94448995-94448996	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs568239897	chr10:94449055-94449056	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs536758535	chr10:94449101-94449102	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs188542981	chr10:94449109-94449110	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs371104417	chr10:94449157-94449158	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs114001966	chr10:94449158-94449159	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs12781513	chr10:94449160-94449161	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs368448352	chr10:94449193-94449194	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs544628160	chr10:94449198-94449199	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs539013549	chr10:94449199-94449200	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs561307515	chr10:94449206-94449207	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs148939627	chr10:94449214-94449215	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs535737516	chr10:94449228-94449229	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs555690607	chr10:94449286-94449287	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs575746087	chr10:94449287-94449288	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs375280193	chr10:94449305-94449306	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs544399912	chr10:94449334-94449335	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs558196263	chr10:94449416-94449417	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs578130983	chr10:94449438-94449439	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs540657123	chr10:94449448-94449449	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs7475059	chr10:94449469-94449470	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs367580592	chr10:94449475-94449476	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs560488859	chr10:94449496-94449497	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs4075563	chr10:94449550-94449551	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs528438935	chr10:94449606-94449607	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs542070126	chr10:94449680-94449681	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs561738313	chr10:94449692-94449693	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs191640546	chr10:94449698-94449699	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs558170145	chr10:94449720-94449721	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs117639730	chr10:94449733-94449734	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs532842622	chr10:94449739-94449740	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs546230628	chr10:94449766-94449767	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs566090388	chr10:94449788-94449789	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs535776260	chr10:94449794-94449795	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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

Chromatin state (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94447800-94450600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr10:94448000-94449200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr10:94448000-94449400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr10:94448200-94448800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
5	chr10:94448200-94448800	Flanking Active TSS	A549	lung
6	chr10:94448200-94449000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr10:94448200-94449000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
8	chr10:94448200-94449000	Flanking Active TSS	Liver	Liver
9	chr10:94448200-94449400	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr10:94448400-94448800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr10:94448400-94448800	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
12	chr10:94448400-94448800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
13	chr10:94448400-94448800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:94448400-94448800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
15	chr10:94448400-94448800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
16	chr10:94448400-94448800	Enhancers	Lung	lung
17	chr10:94448400-94448800	Flanking Active TSS	Rectal Smooth Muscle	rectum
18	chr10:94448400-94449000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
19	chr10:94448400-94449200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr10:94448400-94449200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
21	chr10:94448400-94449200	Flanking Active TSS	HUVEC	blood vessel
22	chr10:94448400-94449400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr10:94448400-94450000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
24	chr10:94448400-94450600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
25	chr10:94448400-94450600	Active TSS	Osteobl	bone
26	chr10:94448400-94451600	Active TSS	NHLF	lung
27	chr10:94448400-94451800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
28	chr10:94448400-94452600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
29	chr10:94448400-94452600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
30	chr10:94448400-94452800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
31	chr10:94448600-94448800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr10:94448600-94448800	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr10:94448600-94448800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
34	chr10:94448600-94448800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr10:94448600-94448800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
36	chr10:94448600-94448800	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr10:94448600-94448800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
38	chr10:94448600-94448800	Flanking Bivalent TSS/Enh	Primary T helper memory cells from peripheral blood 1	blood
39	chr10:94448600-94448800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
40	chr10:94448600-94448800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr10:94448600-94448800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr10:94448600-94448800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr10:94448600-94448800	Bivalent/Poised TSS	Colonic Mucosa	Colon
44	chr10:94448600-94448800	Enhancers	Esophagus	oesophagus
45	chr10:94448600-94448800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
46	chr10:94448600-94448800	Active TSS	Ovary	ovary
47	chr10:94448600-94448800	Active TSS	Rectal Mucosa Donor 31	rectum
48	chr10:94448600-94448800	Active TSS	Right Ventricle	heart
49	chr10:94448600-94448800	Bivalent Enhancer	Small Intestine	intestine
50	chr10:94448600-94448800	Bivalent Enhancer	Stomach Mucosa	stomach

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