Variant report

Variant	nsv1039122
Chromosome Location	chr10:94636267-94693706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1021)
CpG islands
(count:61)
Chromatin interactive
region (count:48)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94640023-94640418	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:94640091-94640529	K562	blood:	n/a	n/a
3	ARID3A	chr10:94646133-94646455	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:94663072-94663981	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:94674281-94674606	K562	blood:	n/a	n/a
6	ARID3A	chr10:94674277-94674603	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:94651891-94652798	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:94644668-94644995	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:94644659-94644946	K562	blood:	n/a	n/a
10	ATF2	chr10:94661632-94662093	GM12878	blood:	n/a	n/a
11	ATF2	chr10:94661764-94662126	GM12878	blood:	n/a	n/a
12	ATF3	chr10:94652012-94652522	A549	lung:	n/a	n/a
13	ATF3	chr10:94651821-94652544	A549	lung:	n/a	n/a
14	BACH1	chr10:94660700-94660714	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr10:94661662-94661961	GM12878	blood:	n/a	n/a
16	BCL3	chr10:94651886-94652742	A549	lung:	n/a	n/a
17	BCL3	chr10:94651801-94652615	A549	lung:	n/a	n/a
18	BCLAF1	chr10:94661722-94662043	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:94654015-94654188	GM12878	blood:	n/a	n/a
20	BHLHE40	chr10:94672456-94672578	K562	blood:	n/a	n/a
21	BHLHE40	chr10:94661634-94662013	GM12878	blood:	n/a	n/a
22	BRCA1	chr10:94652021-94652566	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr10:94652254-94652470	HepG2	liver:	n/a	n/a
24	CBX3	chr10:94651883-94652833	HCT-116	colon:	n/a	n/a
25	CBX3	chr10:94680599-94681034	HCT-116	colon:	n/a	n/a
26	CBX3	chr10:94641497-94641825	K562	blood:	n/a	n/a
27	CBX3	chr10:94651962-94652629	HCT-116	colon:	n/a	n/a
28	CCNT2	chr10:94639824-94639890	K562	blood:	n/a	n/a
29	CEBPB	chr10:94651906-94652391	A549	lung:	n/a	n/a
30	CEBPB	chr10:94675676-94675714	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr10:94651874-94652701	HCT-116	colon:	n/a	n/a
32	CEBPB	chr10:94646030-94646381	IMR90	lung:	n/a	n/a
33	CEBPB	chr10:94651951-94652429	HepG2	liver:	n/a	n/a
34	CEBPB	chr10:94651750-94652669	A549	lung:	n/a	n/a
35	CEBPB	chr10:94651911-94652529	MCF-7	breast:	n/a	n/a
36	CEBPB	chr10:94646050-94646500	A549	lung:	n/a	n/a
37	CEBPB	chr10:94646104-94646345	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:94639782-94640013	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:94677055-94677155	HepG2	liver:	n/a	chr10:94677076-94677085 chr10:94677076-94677085 chr10:94677074-94677085
40	CEBPB	chr10:94652000-94652431	A549	lung:	n/a	n/a
41	CEBPB	chr10:94644129-94644350	K562	blood:	n/a	chr10:94644249-94644262
42	CEBPB	chr10:94674336-94674605	K562	blood:	n/a	n/a
43	CEBPB	chr10:94674359-94674542	IMR90	lung:	n/a	n/a
44	CEBPB	chr10:94651750-94652828	HCT-116	colon:	n/a	n/a
45	CEBPB	chr10:94640184-94640247	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr10:94652096-94652426	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:94651749-94652653	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr10:94677021-94677137	IMR90	lung:	n/a	chr10:94677076-94677085 chr10:94677076-94677085 chr10:94677074-94677085
49	CHD2	chr10:94652138-94652457	HepG2	liver:	n/a	n/a
50	CHD2	chr10:94652062-94652536	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94652135-94652185	SK-N-MC	brain:	n/a
2	chr10:94652135-94652185	SK-N-SH	brain:	n/a
3	chr10:94652135-94652185	HCPEpiC	choroid plexus:	n/a
4	chr10:94652135-94652185	HEEpiC	esophagus:	n/a
5	chr10:94652135-94652185	NH-A	brain:	n/a
6	chr10:94652135-94652185	AG10803	skin:	n/a
7	chr10:94652135-94652185	NT2-D1	testis:	n/a
8	chr10:94652135-94652185	PrEC	prostate:	n/a
9	chr10:94652135-94652185	A549	lung:	n/a
10	chr10:94652135-94652185	NB4	blood:	n/a
11	chr10:94652135-94652185	ovcar-3	ovarian:	n/a
12	chr10:94652135-94652185	U87	brain:	n/a
13	chr10:94652135-94652185	Jurkat	blood:	n/a
14	chr10:94652135-94652185	GM12891	blood:	n/a
15	chr10:94652135-94652185	HepG2	liver:	n/a
16	chr10:94652135-94652185	MCF10A-Er-Src	breast:	n/a
17	chr10:94652135-94652185	Caco-2	colon:	n/a
18	chr10:94652135-94652185	Hepatocyte	liver:	n/a
19	chr10:94652135-94652185	AG09309	skin:	n/a
20	chr10:94652135-94652185	HL-60	blood:	n/a
21	chr10:94652135-94652185	HEK293	kidney:	embryo
22	chr10:94652135-94652185	HIPEpiC	eye:	n/a
23	chr10:94652135-94652185	AG09319	gingival:	n/a
24	chr10:94652135-94652185	CMK	blood:	n/a
25	chr10:94652135-94652185	HMEC	breast:	n/a
26	chr10:94652135-94652185	AG04450	lung:	fetal
27	chr10:94652135-94652185	Hela-S3	cervix:	n/a
28	chr10:94652135-94652185	AoSMC	blood vessel:	n/a
29	chr10:94652135-94652185	GM06990	blood:	n/a
30	chr10:94652135-94652185	GM12892	blood:	n/a
31	chr10:94652135-94652185	HNPCEpiC	eye:	n/a
32	chr10:94652135-94652185	GM12878	blood:	n/a
33	chr10:94652135-94652185	ProgFib	skin:	n/a
34	chr10:94652135-94652185	HCT-116	colon:	n/a
35	chr10:94652135-94652185	T-47D	breast:	n/a
36	chr10:94652135-94652185	LNCaP	prostate:	n/a
37	chr10:94652135-94652185	K562	blood:	n/a
38	chr10:94652135-94652185	H1-hESC	embryonic stem cell:	embryo
39	chr10:94652135-94652185	MCF-7	breast:	n/a
40	chr10:94652135-94652185	HCF	heart:	n/a
41	chr10:94652135-94652185	HCM	heart:	n/a
42	chr10:94652135-94652185	HRPEpiC	eye:	n/a
43	chr10:94652135-94652185	HRCEpiC	kidney:	n/a
44	chr10:94652135-94652185	RPTEC	kidney:	n/a
45	chr10:94652135-94652185	SKMC	muscle:	n/a
46	chr10:94652135-94652185	HUVEC	blood vessel:	n/a
47	chr10:94652135-94652185	HRE	kidney:	n/a
48	chr10:94652135-94652185	ECC-1	luminal epithelium:	n/a
49	chr10:94652135-94652185	IMR90	lung:	fetal
50	chr10:94652135-94652185	NHBE	bronchial:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94633905..94635753-chr10:94639466..94642553,3	K562	blood:
2	chr10:94646541..94648160-chr10:94657093..94659563,2	K562	blood:
3	chr10:94674000..94675687-chr10:94834281..94836039,2	K562	blood:
4	chr10:94634802..94636434-chr10:94636550..94638856,2	MCF-7	breast:
5	chr10:94657045..94660020-chr10:94660295..94662029,2	MCF-7	breast:
6	chr10:94679741..94682175-chr10:94695113..94697468,2	MCF-7	breast:
7	chr10:94333639..94335354-chr10:94637611..94639541,2	MCF-7	breast:
8	chr10:94672230..94674578-chr17:57915271..57917491,2	MCF-7	breast:
9	chr10:94654369..94656417-chr10:94660704..94662374,2	K562	blood:
10	chr10:94674029..94674852-chr10:94724715..94725565,2	MCF-7	breast:
11	chr10:94646541..94648160-chr10:94657093..94659563,2	K562	blood:
12	chr10:94653732..94656423-chr10:94657725..94660166,2	K562	blood:
13	chr10:94673421..94675833-chr10:94685564..94687724,2	MCF-7	breast:
14	chr10:94607903..94609517-chr10:94641022..94642633,2	MCF-7	breast:
15	chr10:94350251..94350770-chr10:94640073..94640678,2	MCF-7	breast:
16	chr10:94654369..94656417-chr10:94660704..94662374,2	K562	blood:
17	chr10:94685883..94688596-chr10:94690517..94693222,3	K562	blood:
18	chr10:94602628..94603467-chr10:94639636..94640258,2	K562	blood:
19	chr10:94686345..94688596-chr10:94691424..94693121,2	K562	blood:
20	chr10:94646967..94648497-chr10:94650916..94652754,2	K562	blood:
21	chr10:94653732..94656423-chr10:94657725..94660166,2	K562	blood:
22	chr10:94646967..94649814-chr10:94651254..94653769,2	K562	blood:
23	chr10:94650650..94651477-chr10:94831181..94832053,2	MCF-7	breast:
24	chr10:94650712..94651345-chr10:95194633..95195177,2	MCF-7	breast:
25	chr10:94623164..94625543-chr10:94648758..94650960,2	K562	blood:
26	chr10:94515577..94518061-chr10:94639001..94640568,2	K562	blood:
27	chr10:94582543..94583333-chr10:94639532..94640277,3	MCF-7	breast:
28	chr10:94693457..94695291-chr10:94697613..94699642,2	MCF-7	breast:
29	chr10:94639799..94640373-chr19:41475219..41475719,2	K562	blood:
30	chr10:94646967..94648497-chr10:94650916..94652754,2	K562	blood:
31	chr10:94653707..94655226-chr10:94655974..94658255,2	MCF-7	breast:
32	chr10:94650712..94651544-chr10:95194677..95195247,2	MCF-7	breast:
33	chr10:94671248..94672935-chr10:94682437..94684217,2	MCF-7	breast:
34	chr10:94652774..94654911-chr10:94796709..94799688,2	MCF-7	breast:
35	chr10:94653707..94655226-chr10:94655974..94658255,2	MCF-7	breast:
36	chr10:94646967..94649814-chr10:94651254..94653769,2	K562	blood:
37	chr10:94644446..94645158-chr10:94724939..94725631,2	MCF-7	breast:
38	chr10:94607070..94611530-chr10:94637347..94641279,5	MCF-7	breast:
39	chr10:94602547..94603439-chr10:94639714..94640841,5	MCF-7	breast:
40	chr10:94643437..94646429-chr10:94647651..94649627,2	K562	blood:
41	chr10:94644359..94645676-chr10:94799255..94800206,4	MCF-7	breast:
42	chr10:94637242..94640461-chr10:94646204..94649459,3	K562	blood:
43	chr10:94652243..94655059-chr10:94655281..94657165,2	K562	blood:
44	chr10:94657045..94660020-chr10:94660295..94662029,2	MCF-7	breast:
45	chr10:94643437..94646429-chr10:94647651..94649627,2	K562	blood:
46	chr10:94671248..94672935-chr10:94682437..94684217,2	MCF-7	breast:
47	chr10:94652243..94655059-chr10:94655281..94657165,2	K562	blood:
48	chr10:94673421..94675833-chr10:94685564..94687724,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP26C1-1	chr10:94669241-94669388	NONHSAT015674
2	lnc-CYP26C1-1	chr10:94675515-94675787	NONHSAT015674

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EXOC6	hsa-miR-31-5p	chr10:94661031-94661052

Variant related genes	Relation type
ENSG00000225118	TF binding region
EXOC6	TF binding region
ENSG00000225118	CpG island
EXOC6	CpG island
ENSG00000062716	chromatin interactions
ENSG00000225118	chromatin interactions
ENSG00000138190	chromatin interactions
ENSG00000119912	chromatin interactions

Extended variants
information (count: 2078 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1409387	chr10:94636367-94636368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565276466	chr10:94636464-94636465	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs536780418	chr10:94636525-94636526	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs557006198	chr10:94636538-94636539	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs59504481	chr10:94636555-94636556	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs545806132	chr10:94636608-94636609	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs71480844	chr10:94636613-94636614	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs188142415	chr10:94636627-94636628	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs138191504	chr10:94636642-94636643	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs61860834	chr10:94636649-94636650	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs11187196	chr10:94636680-94636681	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs35779440	chr10:94636714-94636715	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs67571339	chr10:94636719-94636720	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs71481195	chr10:94636724-94636725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs561701053	chr10:94636725-94636726	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs142781763	chr10:94636780-94636781	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs11187197	chr10:94636781-94636782	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs373706888	chr10:94636798-94636799	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs536821288	chr10:94636838-94636839	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs554739726	chr10:94636919-94636920	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs192733568	chr10:94636963-94636964	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs368841925	chr10:94636988-94636989	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs185015608	chr10:94637025-94637026	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs140421400	chr10:94637051-94637052	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs112492569	chr10:94637110-94637111	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs546979552	chr10:94637114-94637115	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs566517335	chr10:94637122-94637123	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs534645011	chr10:94637123-94637124	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs548060316	chr10:94637220-94637221	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs77476401	chr10:94637245-94637246	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs562882574	chr10:94637312-94637313	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs370930625	chr10:94637495-94637496	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576874652	chr10:94637581-94637582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539120975	chr10:94637613-94637614	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs553046327	chr10:94637666-94637667	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs375116641	chr10:94637699-94637700	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs145034272	chr10:94637726-94637727	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs115784260	chr10:94637730-94637731	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs138863900	chr10:94637746-94637747	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs7069896	chr10:94637817-94637818	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs80218039	chr10:94637824-94637825	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs141866036	chr10:94637870-94637871	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564480049	chr10:94637893-94637894	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533506765	chr10:94637950-94637951	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs546773590	chr10:94637951-94637952	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs111260415	chr10:94637961-94637962	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs61860835	chr10:94638037-94638038	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs189897701	chr10:94638039-94638040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs548934114	chr10:94638102-94638103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs181748705	chr10:94638137-94638138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1002 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94620000-94657600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr10:94624400-94646000	Weak transcription	Fetal Intestine Small	intestine
3	chr10:94633200-94636400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr10:94633200-94640000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr10:94633200-94640200	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr10:94633400-94636400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr10:94633400-94636600	Enhancers	HUVEC	blood vessel
8	chr10:94633400-94656600	Weak transcription	Primary B cells from cord blood	blood
9	chr10:94634800-94636800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr10:94634800-94650400	Weak transcription	Psoas Muscle	Psoas
11	chr10:94636000-94636400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr10:94636000-94637000	Enhancers	Adipose Nuclei	Adipose
13	chr10:94636000-94637200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr10:94636000-94637200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr10:94636000-94637400	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr10:94636000-94637400	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr10:94636000-94637400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr10:94636000-94637400	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr10:94636000-94637400	Enhancers	Liver	Liver
20	chr10:94636000-94637600	Enhancers	Primary T cells from cord blood	blood
21	chr10:94636000-94638200	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr10:94636000-94638400	Enhancers	Primary hematopoietic stem cells	blood
23	chr10:94636000-94638600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr10:94636000-94638600	Enhancers	K562	blood
25	chr10:94636000-94641000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr10:94636200-94636400	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr10:94636200-94637000	Enhancers	Brain Hippocampus Middle	brain
28	chr10:94636200-94637000	Enhancers	A549	lung
29	chr10:94636200-94637200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr10:94636200-94637400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr10:94636200-94639200	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr10:94636400-94636600	Enhancers	Primary T cells fromperipheralblood	blood
33	chr10:94636400-94636600	Enhancers	Right Atrium	heart
34	chr10:94636400-94636600	Enhancers	Dnd41	blood
35	chr10:94636400-94636800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr10:94636400-94637000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr10:94636400-94637000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr10:94636400-94637200	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr10:94636400-94637400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr10:94636400-94637800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr10:94636600-94636800	Flanking Active TSS	HUVEC	blood vessel
42	chr10:94636600-94637200	Enhancers	Brain Angular Gyrus	brain
43	chr10:94636600-94637800	Weak transcription	Right Atrium	heart
44	chr10:94636800-94637000	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr10:94636800-94639800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr10:94636800-94640200	Enhancers	HUVEC	blood vessel
47	chr10:94637000-94637200	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr10:94637000-94637800	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr10:94637000-94638200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr10:94637000-94639800	Weak transcription	A549	lung

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