Variant report

Variant	nsv1025674
Chromosome Location	chr8:48306843-48548862
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2015)
CpG islands
(count:978)
Chromatin interactive
region (count:112)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48352874-48353560	K562	blood:	n/a	chr8:48353449-48353465
2	ARID3A	chr8:48371417-48371596	K562	blood:	n/a	n/a
3	ARID3A	chr8:48437168-48437824	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:48370977-48371215	K562	blood:	n/a	n/a
5	ARID3A	chr8:48521014-48521055	K562	blood:	n/a	n/a
6	ARID3A	chr8:48385021-48385529	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:48531522-48531916	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:48371879-48372001	K562	blood:	n/a	n/a
9	ARID3A	chr8:48469558-48470236	K562	blood:	n/a	n/a
10	ARID3A	chr8:48425108-48425339	HepG2	liver:	n/a	n/a
11	ATF1	chr8:48456323-48456522	K562	blood:	n/a	n/a
12	ATF1	chr8:48370999-48371277	K562	blood:	n/a	n/a
13	ATF1	chr8:48444199-48444363	K562	blood:	n/a	n/a
14	ATF1	chr8:48353062-48353371	K562	blood:	n/a	n/a
15	ATF1	chr8:48469791-48470208	K562	blood:	n/a	n/a
16	ATF2	chr8:48426073-48426690	GM12878	blood:	n/a	n/a
17	ATF2	chr8:48424960-48425389	H1-hESC	embryonic stem cell:	n/a	chr8:48425190-48425201
18	ATF2	chr8:48510510-48511070	GM12878	blood:	n/a	n/a
19	ATF2	chr8:48426005-48426751	GM12878	blood:	n/a	n/a
20	ATF2	chr8:48510596-48510973	GM12878	blood:	n/a	n/a
21	ATF2	chr8:48513192-48513727	GM12878	blood:	n/a	n/a
22	ATF2	chr8:48351488-48352019	GM12878	blood:	n/a	n/a
23	ATF2	chr8:48351620-48351896	GM12878	blood:	n/a	n/a
24	ATF2	chr8:48424919-48425438	H1-hESC	embryonic stem cell:	n/a	chr8:48425190-48425201
25	ATF3	chr8:48424988-48425460	A549	lung:	n/a	chr8:48425192-48425202 chr8:48425189-48425202 chr8:48425192-48425199 chr8:48425188-48425203 chr8:48425189-48425199 chr8:48425190-48425201 chr8:48425192-48425200 chr8:48425188-48425201 chr8:48425189-48425199 chr8:48425189-48425202 chr8:48425192-48425202 chr8:48425190-48425201 chr8:48425190-48425203 chr8:48425189-48425200
26	ATF3	chr8:48424961-48425457	A549	lung:	n/a	chr8:48425192-48425202 chr8:48425189-48425202 chr8:48425192-48425199 chr8:48425188-48425203 chr8:48425189-48425199 chr8:48425190-48425201 chr8:48425192-48425200 chr8:48425188-48425201 chr8:48425189-48425199 chr8:48425189-48425202 chr8:48425192-48425202 chr8:48425190-48425201 chr8:48425190-48425203 chr8:48425189-48425200
27	ATF3	chr8:48510675-48511007	K562	blood:	n/a	n/a
28	ATF3	chr8:48343852-48344341	K562	blood:	n/a	n/a
29	BACH1	chr8:48520911-48521193	K562	blood:	n/a	n/a
30	BACH1	chr8:48344301-48344555	K562	blood:	n/a	n/a
31	BACH1	chr8:48425999-48426602	H1-hESC	embryonic stem cell:	n/a	chr8:48426195-48426209
32	BACH1	chr8:48426078-48426349	K562	blood:	n/a	chr8:48426195-48426209
33	BATF	chr8:48420269-48420728	GM12878	blood:	n/a	n/a
34	BATF	chr8:48351608-48351855	GM12878	blood:	n/a	n/a
35	BATF	chr8:48510570-48510905	GM12878	blood:	n/a	n/a
36	BATF	chr8:48426050-48426304	GM12878	blood:	n/a	chr8:48426194-48426205 chr8:48426195-48426205
37	BATF	chr8:48426321-48426864	GM12878	blood:	n/a	n/a
38	BATF	chr8:48510586-48511006	GM12878	blood:	n/a	n/a
39	BATF	chr8:48351639-48351872	GM12878	blood:	n/a	n/a
40	BATF	chr8:48513236-48513693	GM12878	blood:	n/a	chr8:48513437-48513448
41	BATF	chr8:48513237-48513650	GM12878	blood:	n/a	chr8:48513437-48513448
42	BATF	chr8:48426328-48426884	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:48510615-48510929	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:48486889-48487113	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:48510631-48510906	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:48513234-48513581	GM12878	blood:	n/a	n/a
47	BCL3	chr8:48437371-48437990	A549	lung:	n/a	n/a
48	BCL3	chr8:48437323-48438105	A549	lung:	n/a	n/a
49	BCL3	chr8:48424834-48425773	A549	lung:	n/a	chr8:48425167-48425176
50	BCL3	chr8:48424904-48425461	A549	lung:	n/a	chr8:48425167-48425176

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48418189-48418239	HNPCEpiC	eye:	n/a
2	chr8:48385636-48385686	HAEpiC	amniotic membrane:	n/a
3	chr8:48418189-48418239	HNPCEpiC	eye:	n/a
4	chr8:48385636-48385686	HAEpiC	amniotic membrane:	n/a
5	chr8:48343009-48343059	HIPEpiC	eye:	n/a
6	chr8:48385636-48385686	RPTEC	kidney:	n/a
7	chr8:48474400-48474450	Jurkat	blood:	n/a
8	chr8:48385636-48385686	HepG2	liver:	n/a
9	chr8:48389903-48389953	AG04449	skin:	fetal
10	chr8:48418189-48418239	GM12878	blood:	n/a
11	chr8:48397680-48397730	BJ	skin:	n/a
12	chr8:48437852-48437902	HCF	heart:	n/a
13	chr8:48394027-48394077	HRPEpiC	eye:	n/a
14	chr8:48517420-48517470	NHDF-neo	bronchial:	n/a
15	chr8:48517420-48517470	GM12878	blood:	n/a
16	chr8:48437852-48437902	NHDF-neo	bronchial:	n/a
17	chr8:48389903-48389953	ECC-1	luminal epithelium:	n/a
18	chr8:48474400-48474450	T-47D	breast:	n/a
19	chr8:48397680-48397730	NT2-D1	testis:	n/a
20	chr8:48517420-48517470	HNPCEpiC	eye:	n/a
21	chr8:48325740-48325790	SK-N-SH	brain:	n/a
22	chr8:48389903-48389953	GM19239	blood:	n/a
23	chr8:48344060-48344110	HIPEpiC	eye:	n/a
24	chr8:48325740-48325790	CMK	blood:	n/a
25	chr8:48397680-48397730	CMK	blood:	n/a
26	chr8:48352024-48352074	SK-N-SH_RA	brain:	n/a
27	chr8:48343009-48343059	HL-60	blood:	n/a
28	chr8:48418220-48418270	ovcar-3	ovarian:	n/a
29	chr8:48352024-48352074	HRE	kidney:	n/a
30	chr8:48385636-48385686	GM12891	blood:	n/a
31	chr8:48389903-48389953	Hepatocyte	liver:	n/a
32	chr8:48486091-48486141	SK-N-SH	brain:	n/a
33	chr8:48427018-48427068	NH-A	brain:	n/a
34	chr8:48397680-48397730	AG10803	skin:	n/a
35	chr8:48397680-48397730	HCM	heart:	n/a
36	chr8:48397680-48397730	AG04450	lung:	fetal
37	chr8:48325740-48325790	H1-hESC	embryonic stem cell:	embryo
38	chr8:48389903-48389953	HUVEC	blood vessel:	n/a
39	chr8:48523498-48523548	HEK293	kidney:	embryo
40	chr8:48486091-48486141	HUVEC	blood vessel:	n/a
41	chr8:48394027-48394077	RPTEC	kidney:	n/a
42	chr8:48486091-48486141	GM12892	blood:	n/a
43	chr8:48486091-48486141	HRCEpiC	kidney:	n/a
44	chr8:48427018-48427068	SAEC	small airway:	n/a
45	chr8:48486091-48486141	NHBE	bronchial:	n/a
46	chr8:48523498-48523548	SK-N-SH_RA	brain:	n/a
47	chr8:48389903-48389953	HCM	heart:	n/a
48	chr8:48343009-48343059	Caco-2	colon:	n/a
49	chr8:48389903-48389953	SAEC	small airway:	n/a
50	chr8:48343009-48343059	AG04450	lung:	fetal

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:48301817..48303766-chr8:48305289..48307593,2	MCF-7	breast:
2	chr8:48424729..48427909-chr8:48454789..48458165,3	MCF-7	breast:
3	chr8:48356855..48359120-chr8:48360293..48362250,2	K562	blood:
4	chr8:48431409..48434183-chr8:48649405..48651632,3	K562	blood:
5	chr8:48418430..48420641-chr8:48424490..48426967,2	K562	blood:
6	chr8:48493147..48494925-chr8:48494980..48497854,3	MCF-7	breast:
7	chr8:48320531..48322399-chr8:48323544..48325394,2	MCF-7	breast:
8	chr8:48529219..48530791-chr8:48540316..48542801,2	MCF-7	breast:
9	chr8:48435895..48437509-chr8:48455733..48457442,2	MCF-7	breast:
10	chr8:48367371..48370360-chr8:48387599..48389529,2	MCF-7	breast:
11	chr8:48420026..48420889-chr8:48651231..48651938,2	MCF-7	breast:
12	chr8:48305764..48309024-chr8:53624660..53627223,3	K562	blood:
13	chr8:48316678..48319260-chr8:48343262..48344870,2	MCF-7	breast:
14	chr8:48529413..48532601-chr8:48533499..48535653,4	K562	blood:
15	chr8:48529413..48532601-chr8:48533499..48535653,4	K562	blood:
16	chr6:54711853..54714484-chr8:48522444..48524308,2	MCF-7	breast:
17	chr8:48431010..48432979-chr8:48435160..48436961,2	K562	blood:
18	chr8:48493147..48494925-chr8:48494980..48497854,3	MCF-7	breast:
19	chr8:48513464..48515742-chr8:48650061..48652115,2	MCF-7	breast:
20	chr8:48385290..48387573-chr8:48390610..48393491,2	K562	blood:
21	chr8:48391175..48393987-chr8:48395475..48396988,2	K562	blood:
22	chr8:48421398..48423203-chr8:48423816..48426679,2	K562	blood:
23	chr8:48424864..48427564-chr8:48437009..48439123,4	MCF-7	breast:
24	chr8:48342172..48345072-chr8:48346372..48349504,3	K562	blood:
25	chr8:48490247..48491813-chr8:48492932..48495527,2	MCF-7	breast:
26	chr8:48489915..48491427-chr8:48495181..48498031,2	MCF-7	breast:
27	chr8:48516477..48519191-chr8:48648055..48649779,2	MCF-7	breast:
28	chr8:48333919..48335509-chr8:48339722..48341416,2	K562	blood:
29	chr8:48320531..48322399-chr8:48323544..48325394,2	MCF-7	breast:
30	chr8:48430923..48433623-chr8:48450374..48452837,2	MCF-7	breast:
31	chr8:48507124..48508721-chr8:48509922..48512866,2	MCF-7	breast:
32	chr8:48516911..48521430-chr8:48646759..48650653,4	K562	blood:
33	chr8:48337815..48339899-chr8:48341496..48344035,2	MCF-7	breast:
34	chr8:48391175..48393987-chr8:48395475..48396988,2	K562	blood:
35	chr8:48493400..48495648-chr8:48645566..48647459,2	MCF-7	breast:
36	chr8:48544030..48546745-chr8:48645753..48648082,2	MCF-7	breast:
37	chr8:48507124..48508721-chr8:48509922..48512866,2	MCF-7	breast:
38	chr8:48435225..48441849-chr8:48646333..48652657,17	MCF-7	breast:
39	chr8:48431010..48432979-chr8:48435160..48436961,2	K562	blood:
40	chr8:48316678..48319260-chr8:48343262..48344870,2	MCF-7	breast:
41	chr8:48367371..48370360-chr8:48387599..48389529,2	MCF-7	breast:
42	chr8:48326655..48329493-chr8:48335487..48337638,2	K562	blood:
43	chr8:48338641..48341078-chr8:48342654..48345157,3	K562	blood:
44	chr8:48343800..48344570-chr8:48513956..48514755,2	MCF-7	breast:
45	chr8:48524955..48527562-chr8:48528831..48532011,3	K562	blood:
46	chr8:48355119..48356977-chr8:48650135..48651747,2	MCF-7	breast:
47	chr8:48417465..48419958-chr8:48587324..48588844,2	MCF-7	breast:
48	chr1:234744778..234747020-chr8:48484752..48487431,2	MCF-7	breast:
49	chr8:48529361..48531739-chr8:48533390..48535611,4	K562	blood:
50	chr6:58776812..58777737-chr8:48324823..48325324,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEBPD-3	chr8:48459366-48459968	NONHSAT126450
2	lnc-CEBPD-2	chr8:48504709-48505171	NONHSAT126451
3	lnc-RP11-1134I14.8.1-7	chr8:48439959-48440710	ENSG00000269924.1
4	lnc-CEBPD-3	chr8:48460313-48460488	NONHSAT126450

No data

Variant related genes	Relation type
ENSG00000254065	TF binding region
ENSG00000253330	TF binding region
ENSG00000269924	TF binding region
ENSG00000251354	TF binding region
SPIDR	TF binding region
ENSG00000254065	CpG island
ENSG00000253330	CpG island
ENSG00000269924	CpG island
ENSG00000251354	CpG island
SPIDR	CpG island
ENSG00000164808	chromatin interactions
ENSG00000023287	chromatin interactions
ENSG00000168264	chromatin interactions
ENSG00000269924	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000254065	chromatin interactions
ENSG00000253330	chromatin interactions

Extended variants
information (count: 8727 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:8727 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527753195	chr8:48306928-48306929	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552370234	chr8:48306942-48306943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371891773	chr8:48306974-48306975	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540690145	chr8:48306988-48306989	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562524083	chr8:48307118-48307119	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs367879255	chr8:48307124-48307125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538177689	chr8:48307153-48307154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556579896	chr8:48307154-48307155	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568693954	chr8:48307215-48307216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs74968256	chr8:48307300-48307301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184141210	chr8:48307315-48307316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189431368	chr8:48307355-48307356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572988401	chr8:48307383-48307384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147293578	chr8:48307398-48307399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558814395	chr8:48307413-48307414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577108263	chr8:48307452-48307453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182340984	chr8:48307471-48307472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544535793	chr8:48307492-48307493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562650240	chr8:48307531-48307532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs529954756	chr8:48307547-48307548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186376230	chr8:48307549-48307550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560082932	chr8:48307561-48307562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527816165	chr8:48307578-48307579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552233220	chr8:48307645-48307646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564388830	chr8:48307646-48307647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190779164	chr8:48307649-48307650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531818961	chr8:48307711-48307712	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2130879	chr8:48307712-48307713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs143308600	chr8:48307738-48307739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs536109633	chr8:48307739-48307740	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547910352	chr8:48307751-48307752	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs566452650	chr8:48307773-48307774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533920041	chr8:48307791-48307792	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181507938	chr8:48307796-48307797	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558675478	chr8:48307802-48307803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs115868568	chr8:48307832-48307833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369221586	chr8:48307845-48307846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185707151	chr8:48307851-48307852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556296533	chr8:48307857-48307858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191009242	chr8:48307873-48307874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148600226	chr8:48307938-48307939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542084435	chr8:48307956-48307957	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142074519	chr8:48307970-48307971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572096160	chr8:48307980-48307981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545936687	chr8:48308100-48308101	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564252439	chr8:48308137-48308138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531798918	chr8:48308207-48308208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs200644984	chr8:48308227-48308228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550130958	chr8:48308255-48308256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150735289	chr8:48308280-48308281	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	17142309	CNVD
22q11 deletion syndrome	20357662	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:4497 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48248800-48309600	Weak transcription	Thymus	Thymus
2	chr8:48262400-48309600	Weak transcription	Fetal Stomach	stomach
3	chr8:48278800-48309000	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr8:48279000-48310200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr8:48280600-48311200	Weak transcription	Aorta	Aorta
6	chr8:48282200-48311200	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr8:48282200-48312200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr8:48282400-48321200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr8:48290400-48311400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr8:48290800-48322200	Weak transcription	Liver	Liver
11	chr8:48290800-48347400	Weak transcription	HepG2	liver
12	chr8:48291400-48310000	Weak transcription	Fetal Muscle Trunk	muscle
13	chr8:48291800-48309600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr8:48292000-48310800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:48293000-48312600	Weak transcription	Fetal Thymus	thymus
16	chr8:48293200-48315000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr8:48294400-48309400	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr8:48294400-48309600	Weak transcription	Fetal Intestine Small	intestine
19	chr8:48294800-48309200	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr8:48295800-48311200	Weak transcription	Lung	lung
21	chr8:48295800-48324400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr8:48296200-48308000	Weak transcription	NHDF-Ad	bronchial
23	chr8:48296200-48309200	Weak transcription	Fetal Intestine Large	intestine
24	chr8:48296800-48309600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr8:48297400-48310600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr8:48297400-48312400	Weak transcription	Left Ventricle	heart
27	chr8:48297600-48309800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:48298200-48309000	Weak transcription	Fetal Muscle Leg	muscle
29	chr8:48298200-48310200	Weak transcription	A549	lung
30	chr8:48298200-48310400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:48298200-48325600	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr8:48298400-48309600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr8:48298400-48310800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:48298400-48316400	Weak transcription	NHLF	lung
35	chr8:48298400-48325400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr8:48298600-48308000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr8:48298600-48325600	Weak transcription	Osteobl	bone
38	chr8:48298800-48308000	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr8:48299000-48307400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:48299400-48309200	Weak transcription	Fetal Lung	lung
41	chr8:48299400-48309400	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr8:48299600-48331600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr8:48300000-48307000	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr8:48300000-48309600	Weak transcription	Spleen	Spleen
45	chr8:48300000-48311400	Weak transcription	Esophagus	oesophagus
46	chr8:48300000-48312200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr8:48300000-48318600	Weak transcription	Stomach Mucosa	stomach
48	chr8:48300200-48309600	Weak transcription	Gastric	stomach
49	chr8:48300200-48310200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr8:48300200-48310800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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