Variant report

Variant	nsv482750
Chromosome Location	chr5:178482653-178663586
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1138)
CpG islands
(count:5923)
Chromatin interactive
region (count:78)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1138 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178614256-178614523	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178570502-178570786	K562	blood:	n/a	n/a
3	ARID3A	chr5:178570524-178570804	HepG2	liver:	n/a	n/a
4	ATF1	chr5:178516546-178516874	K562	blood:	n/a	n/a
5	ATF1	chr5:178658394-178658571	K562	blood:	n/a	n/a
6	ATF2	chr5:178570381-178570760	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:178570450-178570822	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr5:178587754-178587897	K562	blood:	n/a	n/a
9	ATF3	chr5:178516536-178516788	K562	blood:	n/a	chr5:178516689-178516699 chr5:178516688-178516703 chr5:178516689-178516702 chr5:178516691-178516711 chr5:178516692-178516702 chr5:178516688-178516701 chr5:178516690-178516701 chr5:178516692-178516700 chr5:178516692-178516699 chr5:178516690-178516701
10	ATF3	chr5:178570449-178570756	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr5:178650528-178650927	GM12878	blood:	n/a	n/a
12	BCL3	chr5:178650193-178650886	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:178594282-178594482	K562	blood:	n/a	n/a
14	BHLHE40	chr5:178594178-178594361	GM12878	blood:	n/a	chr5:178594259-178594275
15	BHLHE40	chr5:178655800-178656133	K562	blood:	n/a	n/a
16	BHLHE40	chr5:178639943-178640216	K562	blood:	n/a	n/a
17	BHLHE40	chr5:178496356-178496412	K562	blood:	n/a	n/a
18	BHLHE40	chr5:178622593-178622738	K562	blood:	n/a	chr5:178622682-178622695
19	BRCA1	chr5:178487152-178487471	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr5:178587627-178587883	K562	blood:	n/a	n/a
21	CCNT2	chr5:178516589-178516784	K562	blood:	n/a	n/a
22	CCNT2	chr5:178594142-178594401	K562	blood:	n/a	n/a
23	CEBPB	chr5:178628215-178628562	K562	blood:	n/a	chr5:178628403-178628414
24	CEBPB	chr5:178648617-178648858	HepG2	liver:	n/a	chr5:178648732-178648743
25	CEBPB	chr5:178628311-178628506	A549	lung:	n/a	chr5:178628403-178628414
26	CEBPB	chr5:178577826-178577892	HepG2	liver:	n/a	chr5:178577847-178577858
27	CEBPB	chr5:178519193-178519255	HepG2	liver:	n/a	chr5:178519229-178519240
28	CEBPB	chr5:178628273-178628533	H1-hESC	embryonic stem cell:	n/a	chr5:178628403-178628414
29	CEBPB	chr5:178491913-178492012	HepG2	liver:	n/a	chr5:178491980-178491991
30	CEBPB	chr5:178628227-178628571	IMR90	lung:	n/a	chr5:178628403-178628414
31	CEBPB	chr5:178628243-178628559	HepG2	liver:	n/a	chr5:178628403-178628414
32	CEBPB	chr5:178648671-178648772	K562	blood:	n/a	chr5:178648732-178648743
33	CEBPB	chr5:178628252-178628543	Hela-S3	cervix:	n/a	chr5:178628403-178628414
34	CHD2	chr5:178654633-178654914	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr5:178487037-178487551	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr5:178614494-178614650	HepG2	liver:	n/a	chr5:178614596-178614606
37	CHD2	chr5:178613153-178613270	HepG2	liver:	n/a	n/a
38	CHD2	chr5:178487228-178487321	GM12878	blood:	n/a	n/a
39	CREB1	chr5:178487083-178487670	A549	lung:	n/a	n/a
40	CREB1	chr5:178487093-178487507	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr5:178487134-178487475	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr5:178655740-178655890	MCF-7	breast:	n/a	chr5:178655843-178655856
43	CTCF	chr5:178570580-178570730	HCT-116	colon:	n/a	n/a
44	CTCF	chr5:178614160-178614310	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr5:178640045-178640142	HepG2	liver:	n/a	chr5:178640071-178640089 chr5:178640073-178640094 chr5:178640074-178640083 chr5:178640072-178640088
46	CTCF	chr5:178613040-178613190	HepG2	liver:	n/a	n/a
47	CTCF	chr5:178594053-178594432	LNCaP	prostate:	n/a	chr5:178594276-178594289 chr5:178594273-178594286 chr5:178594276-178594285 chr5:178594276-178594289 chr5:178594273-178594291 chr5:178594275-178594296 chr5:178594274-178594290 chr5:178594278-178594288
48	CTCF	chr5:178594074-178594402	H1-hESC	embryonic stem cell:	n/a	chr5:178594276-178594289 chr5:178594273-178594286 chr5:178594276-178594285 chr5:178594276-178594289 chr5:178594273-178594291 chr5:178594275-178594296 chr5:178594274-178594290 chr5:178594278-178594288
49	CTCF	chr5:178622980-178623130	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr5:178594122-178594370	GM19238	blood:	n/a	chr5:178594276-178594289 chr5:178594273-178594286 chr5:178594276-178594285 chr5:178594276-178594289 chr5:178594273-178594291 chr5:178594275-178594296 chr5:178594274-178594290 chr5:178594278-178594288

(count:5923 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178622572-178622622	GM06990	blood:	n/a
2	chr5:178487410-178487460	Caco-2	colon:	n/a
3	chr5:178528272-178528322	H1-hESC	embryonic stem cell:	embryo
4	chr5:178636918-178636968	HCF	heart:	n/a
5	chr5:178487576-178487626	HCT-116	colon:	n/a
6	chr5:178561725-178561775	PANC-1	pancreas:	n/a
7	chr5:178622572-178622622	GM06990	blood:	n/a
8	chr5:178487410-178487460	Caco-2	colon:	n/a
9	chr5:178528272-178528322	H1-hESC	embryonic stem cell:	embryo
10	chr5:178636918-178636968	HCF	heart:	n/a
11	chr5:178487576-178487626	HCT-116	colon:	n/a
12	chr5:178561725-178561775	PANC-1	pancreas:	n/a
13	chr5:178622572-178622622	NH-A	brain:	n/a
14	chr5:178487384-178487434	Hepatocyte	liver:	n/a
15	chr5:178547863-178547913	AoSMC	blood vessel:	n/a
16	chr5:178549790-178549840	HRCEpiC	kidney:	n/a
17	chr5:178651200-178651250	ECC-1	luminal epithelium:	n/a
18	chr5:178548700-178548750	IMR90	lung:	fetal
19	chr5:178651074-178651124	HEEpiC	esophagus:	n/a
20	chr5:178547422-178547472	HMEC	breast:	n/a
21	chr5:178660962-178661012	Caco-2	colon:	n/a
22	chr5:178551628-178551678	CMK	blood:	n/a
23	chr5:178598142-178598192	HAEpiC	amniotic membrane:	n/a
24	chr5:178577542-178577592	HRE	kidney:	n/a
25	chr5:178591479-178591529	SK-N-SH_RA	brain:	n/a
26	chr5:178561725-178561775	HCF	heart:	n/a
27	chr5:178487310-178487360	HRE	kidney:	n/a
28	chr5:178564818-178564868	A549	lung:	n/a
29	chr5:178594097-178594147	HepG2	liver:	n/a
30	chr5:178487123-178487173	U87	brain:	n/a
31	chr5:178594097-178594147	AG10803	skin:	n/a
32	chr5:178580645-178580695	H1-hESC	embryonic stem cell:	embryo
33	chr5:178622120-178622170	Hela-S3	cervix:	n/a
34	chr5:178651519-178651569	AG04449	skin:	fetal
35	chr5:178622080-178622130	HCPEpiC	choroid plexus:	n/a
36	chr5:178651074-178651124	HIPEpiC	eye:	n/a
37	chr5:178581108-178581158	SK-N-SH_RA	brain:	n/a
38	chr5:178655042-178655092	SK-N-SH	brain:	n/a
39	chr5:178618678-178618728	GM12892	blood:	n/a
40	chr5:178487485-178487535	GM06990	blood:	n/a
41	chr5:178632502-178632552	GM06990	blood:	n/a
42	chr5:178565721-178565771	NHBE	bronchial:	n/a
43	chr5:178528272-178528322	NH-A	brain:	n/a
44	chr5:178487465-178487515	SK-N-SH	brain:	n/a
45	chr5:178528272-178528322	AG04450	lung:	fetal
46	chr5:178594583-178594633	T-47D	breast:	n/a
47	chr5:178594374-178594424	GM12892	blood:	n/a
48	chr5:178487716-178487766	SK-N-MC	brain:	n/a
49	chr5:178658477-178658527	HL-60	blood:	n/a
50	chr5:178618678-178618728	ovcar-3	ovarian:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:178486462..178489225-chr5:178551148..178554695,3	MCF-7	breast:
2	chr5:178593807..178594987-chr5:178687910..178688845,5	MCF-7	breast:
3	chr5:178594236..178594749-chr5:178920299..178921066,2	K562	blood:
4	chr5:178559035..178560886-chr5:178563328..178565903,2	K562	blood:
5	chr5:178583720..178585825-chr5:178586641..178588375,2	K562	blood:
6	chr5:178486677..178489431-chr5:178490895..178493650,2	MCF-7	breast:
7	chr5:178542353..178545239-chr5:178546502..178548105,2	K562	blood:
8	chr5:178605814..178608090-chr5:178611906..178613466,2	MCF-7	breast:
9	chr5:178488576..178490984-chr5:178494204..178495758,2	MCF-7	breast:
10	chr5:178559035..178560886-chr5:178563328..178565903,2	K562	blood:
11	chr5:178650614..178652876-chr5:178653305..178655920,2	K562	blood:
12	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
13	chr5:178547111..178548841-chr5:178551234..178553296,2	K562	blood:
14	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
15	chr5:178606888..178609097-chr5:178620867..178622421,2	MCF-7	breast:
16	chr1:149223586..149225383-chr5:178547000..178548500,2	MCF-7	breast:
17	chr5:178488576..178490984-chr5:178494204..178495758,2	MCF-7	breast:
18	chr5:178488531..178490916-chr5:178493267..178496128,2	MCF-7	breast:
19	chr5:178650614..178652876-chr5:178653305..178655920,2	K562	blood:
20	chr5:178483088..178485401-chr5:178485853..178487367,2	MCF-7	breast:
21	chr5:178256899..178257517-chr5:178489612..178490272,2	K562	blood:
22	chr5:178508305..178510572-chr5:178515516..178518368,2	K562	blood:
23	chr5:178483751..178486234-chr5:178558590..178560353,2	MCF-7	breast:
24	chr5:178595920..178597681-chr5:178605368..178607876,2	MCF-7	breast:
25	chr5:178606888..178609097-chr5:178620867..178622421,2	MCF-7	breast:
26	chr5:178488531..178490916-chr5:178493267..178496128,2	MCF-7	breast:
27	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
28	chr5:178605814..178608090-chr5:178611906..178613466,2	MCF-7	breast:
29	chr5:178545005..178546733-chr5:178547138..178549506,2	MCF-7	breast:
30	chr5:178579999..178581669-chr5:178587423..178589774,2	MCF-7	breast:
31	chr5:178637418..178640045-chr5:178643551..178645345,3	MCF-7	breast:
32	chr1:149223934..149224436-chr5:178546980..178547500,3	MCF-7	breast:
33	chr5:178619900..178622290-chr5:178622494..178625423,2	MCF-7	breast:
34	chr5:178538154..178541379-chr5:178543841..178547566,3	MCF-7	breast:
35	chr5:178549170..178551463-chr5:178552754..178555057,2	K562	blood:
36	chr5:178599047..178601683-chr5:178602682..178604778,3	K562	blood:
37	chr1:149223402..149225514-chr5:178546980..178548500,3	MCF-7	breast:
38	chr5:178613030..178614553-chr5:178617663..178620440,2	K562	blood:
39	chr5:178570556..178571105-chr5:178687987..178688905,2	MCF-7	breast:
40	chr5:178490747..178493004-chr5:178499608..178501771,2	K562	blood:
41	chr5:178613030..178614553-chr5:178617663..178620440,2	K562	blood:
42	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
43	chr5:178538154..178541379-chr5:178543841..178547566,3	MCF-7	breast:
44	chr5:178649094..178651976-chr5:178660819..178662665,2	MCF-7	breast:
45	chr5:178583720..178585825-chr5:178586641..178588375,2	K562	blood:
46	chr3:64008784..64009514-chr5:178540831..178541760,2	MCF-7	breast:
47	chr5:178483751..178486234-chr5:178558590..178560353,2	MCF-7	breast:
48	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
49	chr5:178286798..178288918-chr5:178487242..178488938,2	MCF-7	breast:
50	chr5:178579999..178581669-chr5:178587423..178589774,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM6-4	chr5:178537854-178540736	NONHSAT105574
2	lnc-GRM6-4	chr5:178537868-178539359	NONHSAT105575

No data

Variant related genes	Relation type
ENSG00000253144	TF binding region
ADAMTS2	TF binding region
ZNF354C	TF binding region
ENSG00000253144	CpG island
ADAMTS2	CpG island
ZNF354C	CpG island
ENSG00000087116	chromatin interactions
ENSG00000253144	chromatin interactions
ENSG00000177932	chromatin interactions
ENSG00000178338	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 8194 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:8194 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117382605	chr5:178482723-178482724	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs551334946	chr5:178482724-178482725	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538765608	chr5:178482726-178482727	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs558681480	chr5:178482736-178482737	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569575364	chr5:178482767-178482768	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs73806848	chr5:178482768-178482769	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182195038	chr5:178482838-178482839	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142658316	chr5:178482844-178482845	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532714547	chr5:178482852-178482853	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs35706936	chr5:178482854-178482855	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs111925216	chr5:178482874-178482875	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138902486	chr5:178482880-178482881	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112538275	chr5:178482885-178482886	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575371517	chr5:178482889-178482890	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs149393862	chr5:178482911-178482912	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs555991475	chr5:178482919-178482920	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187981418	chr5:178482924-178482925	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35298007	chr5:178482967-178482968	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs143954918	chr5:178482970-178482971	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs73806849	chr5:178482990-178482991	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs7711420	chr5:178482994-178482995	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs545625023	chr5:178483009-178483010	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565468097	chr5:178483066-178483067	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs368991866	chr5:178483092-178483093	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527614463	chr5:178483148-178483149	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369703854	chr5:178483155-178483156	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190899788	chr5:178483176-178483177	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138626929	chr5:178483215-178483216	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111613767	chr5:178483247-178483248	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183063816	chr5:178483293-178483294	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188181671	chr5:178483306-178483307	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs193144567	chr5:178483345-178483346	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566802573	chr5:178483401-178483402	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs184934828	chr5:178483431-178483432	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs11749420	chr5:178483445-178483446	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs77994014	chr5:178483495-178483496	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537619699	chr5:178483513-178483514	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188190377	chr5:178483525-178483526	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568327314	chr5:178483544-178483545	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532996889	chr5:178483567-178483568	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535411870	chr5:178483590-178483591	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141624202	chr5:178483594-178483595	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs553725350	chr5:178483596-178483597	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs531321759	chr5:178483602-178483603	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs113924427	chr5:178483610-178483611	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs77206467	chr5:178483615-178483616	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs74515737	chr5:178483662-178483663	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375353915	chr5:178483688-178483689	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192420437	chr5:178483691-178483692	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs113076253	chr5:178483723-178483724	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2831 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178481000-178483600	Enhancers	Placenta Amnion	Placenta Amnion
2	chr5:178481400-178483600	Enhancers	Placenta	Placenta
3	chr5:178482200-178483800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:178482400-178483400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:178482600-178483000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr5:178483000-178486600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:178483400-178487400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:178483600-178487000	Weak transcription	Placenta	Placenta
9	chr5:178483600-178487000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr5:178486400-178486600	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
11	chr5:178486400-178486600	Enhancers	NHDF-Ad	bronchial
12	chr5:178486400-178486800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:178486400-178486800	Active TSS	Adipose Nuclei	Adipose
14	chr5:178486400-178486800	Active TSS	Fetal Lung	lung
15	chr5:178486400-178486800	Active TSS	Skeletal Muscle Female	skeletal muscle
16	chr5:178486400-178487200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
17	chr5:178486400-178488200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr5:178486600-178486800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr5:178486600-178486800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr5:178486600-178486800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr5:178486600-178486800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
22	chr5:178486600-178486800	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr5:178486600-178486800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr5:178486600-178486800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr5:178486600-178486800	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr5:178486600-178486800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr5:178486600-178486800	Enhancers	Liver	Liver
28	chr5:178486600-178486800	ZNF genes & repeats	Brain Anterior Caudate	brain
29	chr5:178486600-178486800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
30	chr5:178486600-178486800	Enhancers	HUVEC	blood vessel
31	chr5:178486600-178487000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:178486600-178487000	Active TSS	Stomach Smooth Muscle	stomach
33	chr5:178486600-178487000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
34	chr5:178486600-178487000	Flanking Active TSS	NHDF-Ad	bronchial
35	chr5:178486600-178487200	Active TSS	Brain Germinal Matrix	brain
36	chr5:178486600-178487200	ZNF genes & repeats	A549	lung
37	chr5:178486600-178487800	Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr5:178486600-178487800	Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr5:178486600-178487800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:178486600-178487800	Active TSS	Brain Hippocampus Middle	brain
41	chr5:178486600-178487800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr5:178486600-178487800	Active TSS	Duodenum Mucosa	Duodenum
43	chr5:178486600-178487800	Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr5:178486600-178487800	Active TSS	Fetal Heart	heart
45	chr5:178486600-178487800	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr5:178486600-178487800	Active TSS	Right Atrium	heart
47	chr5:178486600-178488000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
48	chr5:178486600-178488000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr5:178486600-178488000	Active TSS	Brain Angular Gyrus	brain
50	chr5:178486600-178488000	Active TSS	Colon Smooth Muscle	Colon

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