Variant report

Variant	nsv522415
Chromosome Location	chr10:5721653-5768493
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1486)
CpG islands
(count:1284)
Chromatin interactive
region (count:106)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1486 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5729263-5729288	K562	blood:	n/a	n/a
2	ARID3A	chr10:5727547-5727942	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5739648-5740302	K562	blood:	n/a	n/a
4	ARID3A	chr10:5726405-5726932	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:5736177-5736325	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:5738365-5738366	K562	blood:	n/a	n/a
7	ARID3A	chr10:5727377-5728147	K562	blood:	n/a	n/a
8	ARID3A	chr10:5734681-5735376	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:5734791-5734856	K562	blood:	n/a	n/a
10	ATF1	chr10:5726348-5726801	K562	blood:	n/a	n/a
11	ATF1	chr10:5723928-5724210	K562	blood:	n/a	n/a
12	ATF1	chr10:5727240-5727810	K562	blood:	n/a	n/a
13	ATF2	chr10:5734707-5735139	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr10:5726261-5726744	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr10:5734574-5734857	K562	blood:	n/a	n/a
16	ATF3	chr10:5727102-5727708	K562	blood:	n/a	n/a
17	ATF3	chr10:5727076-5727501	K562	blood:	n/a	n/a
18	ATF3	chr10:5726344-5726712	K562	blood:	n/a	n/a
19	BACH1	chr10:5726221-5727779	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr10:5723929-5724539	K562	blood:	n/a	n/a
21	BACH1	chr10:5734414-5735236	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr10:5734963-5735160	K562	blood:	n/a	n/a
23	BACH1	chr10:5746580-5746627	K562	blood:	n/a	n/a
24	BCL3	chr10:5726037-5726771	A549	lung:	n/a	chr10:5726742-5726751
25	BCL3	chr10:5725948-5727052	A549	lung:	n/a	chr10:5726742-5726751
26	BCLAF1	chr10:5734444-5735296	GM12878	blood:	n/a	chr10:5734833-5734846 chr10:5735089-5735102
27	BCLAF1	chr10:5726969-5727642	K562	blood:	n/a	chr10:5727452-5727459 chr10:5727211-5727224
28	BCLAF1	chr10:5726190-5726921	K562	blood:	n/a	chr10:5726742-5726751
29	BCLAF1	chr10:5734492-5735055	GM12878	blood:	n/a	chr10:5734833-5734846
30	BCLAF1	chr10:5726211-5727021	GM12878	blood:	n/a	chr10:5726742-5726751
31	BCLAF1	chr10:5727253-5727814	GM12878	blood:	n/a	chr10:5727452-5727459
32	BHLHE40	chr10:5726350-5727065	HepG2	liver:	n/a	n/a
33	BHLHE40	chr10:5727321-5727820	GM12878	blood:	n/a	n/a
34	BHLHE40	chr10:5726143-5727797	K562	blood:	n/a	chr10:5727206-5727222
35	BHLHE40	chr10:5723983-5724150	HepG2	liver:	n/a	n/a
36	BHLHE40	chr10:5734605-5735204	HepG2	liver:	n/a	n/a
37	BHLHE40	chr10:5734348-5735479	GM12878	blood:	n/a	n/a
38	BHLHE40	chr10:5729254-5729502	GM12878	blood:	n/a	n/a
39	BHLHE40	chr10:5726217-5727086	GM12878	blood:	n/a	n/a
40	BHLHE40	chr10:5723827-5724252	K562	blood:	n/a	n/a
41	BHLHE40	chr10:5734654-5735364	K562	blood:	n/a	n/a
42	BRCA1	chr10:5726258-5726856	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr10:5726374-5726745	GM12878	blood:	n/a	n/a
44	BRCA1	chr10:5727068-5727101	HepG2	liver:	n/a	n/a
45	BRCA1	chr10:5726308-5726893	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr10:5726326-5726767	HepG2	liver:	n/a	n/a
47	BRCA1	chr10:5734748-5734948	HepG2	liver:	n/a	n/a
48	CBX3	chr10:5726924-5727812	K562	blood:	n/a	n/a
49	CBX3	chr10:5734564-5735338	K562	blood:	n/a	n/a
50	CBX3	chr10:5726145-5726722	K562	blood:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5726677-5726727	GM12878	blood:	n/a
2	chr10:5724021-5724071	PrEC	prostate:	n/a
3	chr10:5726677-5726727	HCM	heart:	n/a
4	chr10:5726677-5726727	GM12878	blood:	n/a
5	chr10:5724021-5724071	PrEC	prostate:	n/a
6	chr10:5726677-5726727	HCM	heart:	n/a
7	chr10:5727926-5727976	Hepatocyte	liver:	n/a
8	chr10:5726819-5726869	NHBE	bronchial:	n/a
9	chr10:5734571-5734621	HEK293	kidney:	embryo
10	chr10:5727926-5727976	HCT-116	colon:	n/a
11	chr10:5734571-5734621	GM12878	blood:	n/a
12	chr10:5728078-5728128	HL-60	blood:	n/a
13	chr10:5726702-5726752	K562	blood:	n/a
14	chr10:5734716-5734766	HRCEpiC	kidney:	n/a
15	chr10:5727808-5727858	AG04449	skin:	fetal
16	chr10:5726438-5726488	CMK	blood:	n/a
17	chr10:5726699-5726749	AG04449	skin:	fetal
18	chr10:5726466-5726516	ProgFib	skin:	n/a
19	chr10:5726702-5726752	SAEC	small airway:	n/a
20	chr10:5727926-5727976	SK-N-SH	brain:	n/a
21	chr10:5726466-5726516	MCF10A-Er-Src	breast:	n/a
22	chr10:5734985-5735035	H1-hESC	embryonic stem cell:	embryo
23	chr10:5727416-5727466	SKMC	muscle:	n/a
24	chr10:5724021-5724071	GM06990	blood:	n/a
25	chr10:5734985-5735035	NH-A	brain:	n/a
26	chr10:5726650-5726700	MCF10A-Er-Src	breast:	n/a
27	chr10:5727926-5727976	NHBE	bronchial:	n/a
28	chr10:5726683-5726733	HepG2	liver:	n/a
29	chr10:5735135-5735185	K562	blood:	n/a
30	chr10:5726702-5726752	GM19239	blood:	n/a
31	chr10:5734571-5734621	K562	blood:	n/a
32	chr10:5727477-5727527	NH-A	brain:	n/a
33	chr10:5734716-5734766	ProgFib	skin:	n/a
34	chr10:5734571-5734621	NT2-D1	testis:	n/a
35	chr10:5726677-5726727	HRPEpiC	eye:	n/a
36	chr10:5726702-5726752	AG04449	skin:	fetal
37	chr10:5726631-5726681	HepG2	liver:	n/a
38	chr10:5735135-5735185	AG09319	gingival:	n/a
39	chr10:5734571-5734621	MCF-7	breast:	n/a
40	chr10:5735349-5735399	NB4	blood:	n/a
41	chr10:5735349-5735399	GM12891	blood:	n/a
42	chr10:5735349-5735399	GM12892	blood:	n/a
43	chr10:5727926-5727976	K562	blood:	n/a
44	chr10:5727416-5727466	K562	blood:	n/a
45	chr10:5734716-5734766	HCPEpiC	choroid plexus:	n/a
46	chr10:5734571-5734621	AG09319	gingival:	n/a
47	chr10:5734571-5734621	BJ	skin:	n/a
48	chr10:5727926-5727976	HCF	heart:	n/a
49	chr10:5726819-5726869	HRE	kidney:	n/a
50	chr10:5726702-5726752	HCPEpiC	choroid plexus:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:5722939..5725566-chr10:5730999..5734048,3	K562	blood:
2	chr10:5728757..5730539-chr10:5931112..5932706,2	K562	blood:
3	chr10:5484441..5486510-chr10:5728306..5731305,2	MCF-7	breast:
4	chr10:5749331..5751583-chr10:5752146..5753784,2	MCF-7	breast:
5	chr10:5726410..5728417-chr10:5738015..5741917,3	MCF-7	breast:
6	chr10:5722939..5725566-chr10:5730999..5734048,3	K562	blood:
7	chr10:5758294..5759916-chr10:5768801..5770809,2	K562	blood:
8	chr10:5726775..5729176-chr10:5734287..5736106,2	MCF-7	breast:
9	chr10:5674655..5677112-chr10:5724421..5726297,2	K562	blood:
10	chr10:5758553..5760843-chr10:5766010..5768055,2	MCF-7	breast:
11	chr10:5487726..5489985-chr10:5734513..5736734,3	K562	blood:
12	chr10:5725239..5726746-chr10:5852889..5855526,2	K562	blood:
13	chr10:5713284..5716220-chr10:5720012..5722178,2	MCF-7	breast:
14	chr10:5757345..5759947-chr10:5761882..5764434,2	K562	blood:
15	chr10:5725406..5728715-chr10:5747568..5751515,5	MCF-7	breast:
16	chr10:5725094..5729377-chr10:5927689..5933777,6	MCF-7	breast:
17	chr10:5725933..5727611-chr10:5766306..5768774,2	MCF-7	breast:
18	chr10:5754503..5756653-chr10:5756794..5759759,2	K562	blood:
19	chr10:5748194..5752835-chr10:5754048..5756817,4	MCF-7	breast:
20	chr10:5762001..5764340-chr10:5764704..5766280,2	K562	blood:
21	chr10:5733360..5736300-chr10:5737628..5741126,5	MCF-7	breast:
22	chr10:5726952..5729225-chr10:5806393..5808626,2	MCF-7	breast:
23	chr10:4911567..4913119-chr10:5727909..5730757,2	K562	blood:
24	chr10:5726042..5728288-chr10:5749073..5750602,2	MCF-7	breast:
25	chr10:5734758..5736346-chr10:5739333..5741720,2	MCF-7	breast:
26	chr10:5727488..5729665-chr10:5929692..5932614,2	MCF-7	breast:
27	chr10:5725427..5729550-chr10:5853446..5856157,4	MCF-7	breast:
28	chr10:5739796..5741781-chr10:5749171..5751664,2	K562	blood:
29	chr10:5762001..5764340-chr10:5764704..5766280,2	K562	blood:
30	chr10:5696053..5698803-chr10:5727232..5729360,2	K562	blood:
31	chr10:5487728..5489402-chr10:5743832..5746682,2	MCF-7	breast:
32	chr10:5725704..5728346-chr3:33480193..33482855,3	MCF-7	breast:
33	chr10:5707719..5709670-chr10:5755550..5758097,2	MCF-7	breast:
34	chr10:5726775..5729176-chr10:5734287..5736106,2	MCF-7	breast:
35	chr10:5733731..5736743-chr10:5750015..5755601,4	MCF-7	breast:
36	chr10:5721909..5724217-chr10:5930242..5932210,2	K562	blood:
37	chr10:5748194..5752835-chr10:5754048..5756817,4	MCF-7	breast:
38	chr10:5733545..5736331-chr10:5766284..5768389,2	K562	blood:
39	chr10:5758553..5760843-chr10:5766010..5768055,2	MCF-7	breast:
40	chr10:5766311..5769267-chr10:5770852..5774721,4	K562	blood:
41	chr10:5673292..5677112-chr10:5724421..5727333,4	K562	blood:
42	chr10:5748091..5753661-chr10:5757526..5761076,4	K562	blood:
43	chr10:5727335..5729854-chr10:5777449..5779108,2	K562	blood:
44	chr10:5585750..5587884-chr10:5738818..5740542,2	K562	blood:
45	chr10:5725582..5728827-chr10:5752793..5758658,6	MCF-7	breast:
46	chr10:5704788..5710194-chr10:5724908..5728833,8	K562	blood:
47	chr10:5751112..5753798-chr10:5754382..5757716,3	K562	blood:
48	chr10:5719546..5721804-chr10:5852242..5853949,2	K562	blood:
49	chr10:5715613..5722636-chr10:5722933..5730555,14	MCF-7	breast:
50	chr10:5725503..5729426-chr10:5853777..5860412,5	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM208B-2	chr10:5723454-5723961	NONHSAT011173
2	lnc-CALML3-1	chr10:5754357-5754502	NONHSAT011176
3	lnc-CALML3-1	chr10:5754786-5754881	NONHSAT011175
4	lnc-GDI2-1	chr10:5754383-5754651	ENSG00000226647.2
5	lnc-FAM208B-1	chr10:5724483-5725287	NONHSAT011174
6	lnc-CALML3-1	chr10:5759622-5759713	NONHSAT011175
7	lnc-CALML3-1	chr10:5754786-5754835	NONHSAT011176
8	lnc-CALML3-1	chr10:5741411-5741700	NONHSAT011177
9	lnc-CALML3-1	chr10:5762507-5762574	NONHSAT011175
10	lnc-CALML3-1	chr10:5751493-5751626	NONHSAT011177
11	lnc-CALML3-1	chr10:5726928-5727138	NONHSAT011175
12	lnc-CALML3-1	chr10:5751493-5751626	NONHSAT011176
13	lnc-GDI2-1	chr10:5755711-5756386	ENSG00000226647.2
14	lnc-GDI2-1	chr10:5754177-5754651	ENSG00000226647.1
15	lnc-GDI2-1	chr10:5754137-5754651	ENSG00000226647.2
16	lnc-CALML3-1	chr10:5734779-5734881	NONHSAT011176
17	lnc-CALML3-1	chr10:5756098-5756170	NONHSAT011175

No data

Variant related genes	Relation type
FAM208B	TF binding region
ENSG00000226647	TF binding region
FAM208B	CpG island
ENSG00000226647	CpG island
ENSG00000108021	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000153560	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000134461	chromatin interactions
ENSG00000272764	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000196372	chromatin interactions
ENSG00000240577	chromatin interactions
ENSG00000226647	chromatin interactions

Extended variants
information (count: 1782 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1782 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2386626	chr10:5721653-5721654	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78135803	chr10:5721701-5721702	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs532672675	chr10:5721742-5721743	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs547550037	chr10:5721812-5721813	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs566690271	chr10:5721865-5721866	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs533747319	chr10:5721906-5721907	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs555493434	chr10:5721922-5721923	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs114985114	chr10:5721971-5721972	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs144655198	chr10:5721980-5721981	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs9423906	chr10:5722020-5722021	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs569118012	chr10:5722044-5722045	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs537864918	chr10:5722057-5722058	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs570099030	chr10:5722072-5722073	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs112077101	chr10:5722119-5722120	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs114390393	chr10:5722152-5722153	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs544739161	chr10:5722162-5722163	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs558001369	chr10:5722226-5722227	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs191096478	chr10:5722318-5722319	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs9424185	chr10:5722326-5722327	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs542855253	chr10:5722327-5722328	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs561490992	chr10:5722336-5722337	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs532059089	chr10:5722507-5722508	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs377484885	chr10:5722532-5722533	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs544098999	chr10:5722534-5722535	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs565305887	chr10:5722544-5722545	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs4750473	chr10:5722561-5722562	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs375189832	chr10:5722584-5722585	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs183282614	chr10:5722601-5722602	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs9424186	chr10:5722602-5722603	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs1578744	chr10:5722616-5722617	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs561385725	chr10:5722630-5722631	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs200392119	chr10:5722632-5722633	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs530171463	chr10:5722695-5722696	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs34912376	chr10:5722744-5722745	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs386370557	chr10:5722745-5722746	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs397846381	chr10:5722755-5722756	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs1578743	chr10:5722784-5722785	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs11258907	chr10:5722789-5722790	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs9423907	chr10:5722793-5722794	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs9423908	chr10:5722839-5722840	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs72774040	chr10:5722840-5722841	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs538251826	chr10:5722888-5722889	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs553682003	chr10:5722889-5722890	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs368843567	chr10:5722922-5722923	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs9424189	chr10:5722942-5722943	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs554884218	chr10:5722951-5722952	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs9423909	chr10:5722952-5722953	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs544592780	chr10:5722980-5722981	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs187978155	chr10:5723029-5723030	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs565566388	chr10:5723076-5723077	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1902 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5720000-5726000	Weak transcription	Thymus	Thymus
2	chr10:5720400-5722200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:5720400-5725800	Weak transcription	Fetal Thymus	thymus
4	chr10:5720600-5721800	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr10:5720600-5723200	Weak transcription	K562	blood
6	chr10:5721200-5722000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr10:5721400-5722200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr10:5721800-5722200	Enhancers	NHDF-Ad	bronchial
9	chr10:5721800-5726000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr10:5722000-5726000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:5722200-5726000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr10:5722200-5726000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr10:5722200-5726000	Weak transcription	NHDF-Ad	bronchial
14	chr10:5723200-5723800	Enhancers	K562	blood
15	chr10:5723400-5726000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr10:5723600-5724400	Enhancers	NHEK	skin
17	chr10:5723800-5724800	Flanking Active TSS	K562	blood
18	chr10:5723800-5725200	Enhancers	HepG2	liver
19	chr10:5724400-5726000	Weak transcription	NHEK	skin
20	chr10:5724800-5726000	Enhancers	K562	blood
21	chr10:5725000-5725200	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr10:5725200-5726000	Weak transcription	HepG2	liver
23	chr10:5725800-5726000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr10:5725800-5726000	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr10:5725800-5726000	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr10:5725800-5726000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr10:5725800-5726000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:5725800-5726000	Active TSS	Adipose Nuclei	Adipose
29	chr10:5725800-5726000	Enhancers	Brain Anterior Caudate	brain
30	chr10:5725800-5726000	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr10:5725800-5726000	Enhancers	Colon Smooth Muscle	Colon
32	chr10:5725800-5726000	Enhancers	Duodenum Mucosa	Duodenum
33	chr10:5725800-5726000	Enhancers	Fetal Kidney	kidney
34	chr10:5725800-5726000	Enhancers	Rectal Smooth Muscle	rectum
35	chr10:5725800-5726200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr10:5725800-5726200	Enhancers	Fetal Thymus	thymus
37	chr10:5725800-5726400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
38	chr10:5725800-5726600	Flanking Active TSS	Dnd41	blood
39	chr10:5726000-5726200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
40	chr10:5726000-5726200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr10:5726000-5726200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
42	chr10:5726000-5726200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
43	chr10:5726000-5726200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr10:5726000-5726200	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr10:5726000-5726200	Enhancers	Primary B cells from peripheral blood	blood
46	chr10:5726000-5726200	Enhancers	Primary T cells from cord blood	blood
47	chr10:5726000-5726200	Enhancers	Primary hematopoietic stem cells	blood
48	chr10:5726000-5726200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr10:5726000-5726200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr10:5726000-5726200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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