Variant report

Variant	nsv607726
Chromosome Location	chr7:87040629-87139316
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1361)
CpG islands
(count:1037)
Chromatin interactive
region (count:84)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:87046062-87046357	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:87044141-87044339	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:87103805-87104061	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:87126805-87127218	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:87105129-87105319	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:87046029-87046336	K562	blood:	n/a	n/a
7	ARID3A	chr7:87093353-87093783	HepG2	liver:	n/a	n/a
8	ATF1	chr7:87068362-87068484	K562	blood:	n/a	n/a
9	ATF1	chr7:87080871-87080985	K562	blood:	n/a	n/a
10	ATF2	chr7:87075193-87075772	GM12878	blood:	n/a	n/a
11	ATF2	chr7:87075213-87075701	GM12878	blood:	n/a	n/a
12	ATF2	chr7:87103159-87104838	GM12878	blood:	n/a	chr7:87104394-87104401
13	ATF2	chr7:87103357-87104743	GM12878	blood:	n/a	chr7:87104394-87104401
14	BACH1	chr7:87104693-87104885	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr7:87094518-87094660	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr7:87103408-87104590	GM12878	blood:	n/a	chr7:87104368-87104377
17	BATF	chr7:87103714-87104408	GM12878	blood:	n/a	chr7:87104368-87104377
18	BATF	chr7:87075232-87075613	GM12878	blood:	n/a	n/a
19	BATF	chr7:87128225-87128461	GM12878	blood:	n/a	chr7:87128304-87128313
20	BCL11A	chr7:87075188-87075625	GM12878	blood:	n/a	chr7:87075396-87075405
21	BCL11A	chr7:87103389-87104608	GM12878	blood:	n/a	chr7:87103426-87103435
22	BCL11A	chr7:87075212-87075653	GM12878	blood:	n/a	chr7:87075396-87075405
23	BCL11A	chr7:87103765-87104455	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:87128122-87128426	GM12878	blood:	n/a	n/a
25	BCL3	chr7:87103501-87104527	GM12878	blood:	n/a	n/a
26	BCL3	chr7:87103771-87104306	GM12878	blood:	n/a	n/a
27	BCLAF1	chr7:87103284-87104672	GM12878	blood:	n/a	chr7:87103426-87103435
28	BCLAF1	chr7:87103241-87104577	GM12878	blood:	n/a	chr7:87103426-87103435
29	BCLAF1	chr7:87045947-87046408	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:87046015-87046328	K562	blood:	n/a	n/a
31	BHLHE40	chr7:87105560-87105599	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:87049681-87049784	K562	blood:	n/a	n/a
33	BHLHE40	chr7:87103333-87105002	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:87093399-87093797	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:87138119-87138238	K562	blood:	n/a	n/a
36	BHLHE40	chr7:87075261-87075645	GM12878	blood:	n/a	n/a
37	BRCA1	chr7:87093351-87093701	HepG2	liver:	n/a	n/a
38	BRCA1	chr7:87043607-87043797	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr7:87105230-87105252	GM12878	blood:	n/a	n/a
40	BRCA1	chr7:87104037-87104253	GM12878	blood:	n/a	n/a
41	BRCA1	chr7:87135480-87135959	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr7:87065015-87065221	Hela-S3	cervix:	n/a	n/a
43	CCNT2	chr7:87089363-87089563	K562	blood:	n/a	n/a
44	CCNT2	chr7:87105224-87105341	K562	blood:	n/a	n/a
45	CEBPB	chr7:87044088-87044304	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:87093392-87093696	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:87104224-87104575	A549	lung:	n/a	n/a
48	CEBPB	chr7:87126202-87126480	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:87104216-87104585	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:87104255-87104498	Hela-S3	cervix:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:87042706-87042756	RPTEC	kidney:	n/a
2	chr7:87104879-87104929	MCF-7	breast:	n/a
3	chr7:87104879-87104929	NH-A	brain:	n/a
4	chr7:87104879-87104929	GM06990	blood:	n/a
5	chr7:87109799-87109849	Jurkat	blood:	n/a
6	chr7:87109799-87109849	MCF-7	breast:	n/a
7	chr7:87042706-87042756	AG04450	lung:	fetal
8	chr7:87103624-87103674	CMK	blood:	n/a
9	chr7:87104724-87104774	PANC-1	pancreas:	n/a
10	chr7:87109799-87109849	CMK	blood:	n/a
11	chr7:87104879-87104929	HRE	kidney:	n/a
12	chr7:87093634-87093684	HL-60	blood:	n/a
13	chr7:87109799-87109849	HRE	kidney:	n/a
14	chr7:87104932-87104982	AG04450	lung:	fetal
15	chr7:87104879-87104929	PrEC	prostate:	n/a
16	chr7:87093634-87093684	PFSK-1	brain:	n/a
17	chr7:87093634-87093684	NH-A	brain:	n/a
18	chr7:87105398-87105448	HCF	heart:	n/a
19	chr7:87105398-87105448	SAEC	small airway:	n/a
20	chr7:87104879-87104929	U87	brain:	n/a
21	chr7:87105022-87105072	HIPEpiC	eye:	n/a
22	chr7:87105293-87105343	HCPEpiC	choroid plexus:	n/a
23	chr7:87105216-87105266	GM12891	blood:	n/a
24	chr7:87105216-87105266	HRE	kidney:	n/a
25	chr7:87105022-87105072	AoSMC	blood vessel:	n/a
26	chr7:87042706-87042756	HAEpiC	amniotic membrane:	n/a
27	chr7:87104879-87104929	BE2_C	brain:	n/a
28	chr7:87109370-87109420	GM12878	blood:	n/a
29	chr7:87105293-87105343	BE2_C	brain:	n/a
30	chr7:87105293-87105343	HCT-116	colon:	n/a
31	chr7:87104879-87104929	T-47D	breast:	n/a
32	chr7:87105216-87105266	Hela-S3	cervix:	n/a
33	chr7:87105416-87105466	SKMC	muscle:	n/a
34	chr7:87105416-87105466	HNPCEpiC	eye:	n/a
35	chr7:87109319-87109369	U87	brain:	n/a
36	chr7:87104879-87104929	HUVEC	blood vessel:	n/a
37	chr7:87105293-87105343	HEK293	kidney:	embryo
38	chr7:87109370-87109420	HNPCEpiC	eye:	n/a
39	chr7:87104932-87104982	SK-N-SH_RA	brain:	n/a
40	chr7:87105022-87105072	CMK	blood:	n/a
41	chr7:87105416-87105466	HL-60	blood:	n/a
42	chr7:87109319-87109369	SK-N-SH	brain:	n/a
43	chr7:87109319-87109369	MCF10A-Er-Src	breast:	n/a
44	chr7:87104879-87104929	AG09309	skin:	n/a
45	chr7:87104879-87104929	GM19239	blood:	n/a
46	chr7:87093634-87093684	AoSMC	blood vessel:	n/a
47	chr7:87104724-87104774	SAEC	small airway:	n/a
48	chr7:87108287-87108337	RPTEC	kidney:	n/a
49	chr7:87104932-87104982	HCF	heart:	n/a
50	chr7:87105416-87105466	HPAEpiC	pulmonary alveolar:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:87119310..87120989-chr7:87123250..87124879,2	K562	blood:
2	chr7:87042243..87044044-chr7:87044157..87046245,3	MCF-7	breast:
3	chr7:86991467..86994068-chr7:87051605..87053825,2	MCF-7	breast:
4	chr7:87056485..87058052-chr7:87059900..87061514,2	K562	blood:
5	chr7:86981093..86983879-chr7:87038872..87041059,2	MCF-7	breast:
6	chr7:87121870..87124695-chr7:87125654..87129422,3	K562	blood:
7	chr7:87039253..87041536-chr7:87044020..87045939,2	K562	blood:
8	chr7:87048856..87050665-chr7:87056840..87059034,2	MCF-7	breast:
9	chr7:86780861..86783739-chr7:87044676..87047571,2	K562	blood:
10	chr7:86941251..86942248-chr7:87045584..87047452,18	MCF-7	breast:
11	chr7:86941366..86942177-chr7:87136531..87137084,2	MCF-7	breast:
12	chr7:87120648..87122602-chr7:87127375..87130104,3	K562	blood:
13	chr7:87064944..87067466-chr7:87067483..87069471,2	MCF-7	breast:
14	chr7:86848274..86850901-chr7:87061443..87064403,3	MCF-7	breast:
15	chr7:86967043..86968640-chr7:87043490..87046255,2	MCF-7	breast:
16	chr7:87026550..87029419-chr7:87039451..87043788,3	MCF-7	breast:
17	chr7:87042569..87044840-chr7:87046339..87049355,4	MCF-7	breast:
18	chr7:86781692..86783648-chr7:87052810..87055200,2	MCF-7	breast:
19	chr7:87044946..87047551-chr7:87049073..87051453,2	MCF-7	breast:
20	chr7:87051942..87054838-chr7:87071863..87073802,2	K562	blood:
21	chr7:87044946..87047551-chr7:87049073..87051453,2	MCF-7	breast:
22	chr7:86848705..86851193-chr7:87044626..87046849,2	MCF-7	breast:
23	chr7:86972942..86975537-chr7:87069538..87072015,2	MCF-7	breast:
24	chr7:87059548..87061142-chr7:87062685..87064346,3	K562	blood:
25	chr7:87048856..87050665-chr7:87056840..87059034,2	MCF-7	breast:
26	chr7:87135658..87136343-chr7:87515955..87516855,2	MCF-7	breast:
27	chr7:87040455..87042018-chr7:87042195..87043888,2	MCF-7	breast:
28	chr7:87051942..87054838-chr7:87071863..87073802,2	K562	blood:
29	chr7:86941321..86942494-chr7:87045634..87046678,6	MCF-7	breast:
30	chr7:87040455..87042018-chr7:87042195..87043888,2	MCF-7	breast:
31	chr7:87042569..87044840-chr7:87046339..87049355,4	MCF-7	breast:
32	chr7:87025082..87026889-chr7:87040768..87042913,2	K562	blood:
33	chr7:86941239..86942263-chr7:87043678..87045087,6	K562	blood:
34	chr7:86940706..86943754-chr7:87040943..87048765,8	MCF-7	breast:
35	chr7:87042243..87044044-chr7:87044157..87046245,3	MCF-7	breast:
36	chr7:87075903..87078103-chr7:87080060..87082449,2	K562	blood:
37	chr7:87136911..87137500-chr7:87193384..87194119,2	MCF-7	breast:
38	chr7:87121870..87124695-chr7:87125654..87129422,3	K562	blood:
39	chr7:87020157..87022071-chr7:87039482..87041620,2	K562	blood:
40	chr7:87064944..87067466-chr7:87067483..87069471,2	MCF-7	breast:
41	chr7:87036333..87038617-chr7:87054142..87056199,2	K562	blood:
42	chr7:87126316..87128624-chr7:87132901..87135046,3	K562	blood:
43	chr7:87043780..87045715-chr7:87084104..87086345,2	MCF-7	breast:
44	chr7:87064330..87066764-chr7:87067722..87070554,3	K562	blood:
45	chr7:86941297..86942296-chr7:87045682..87046950,19	K562	blood:
46	chr7:87027992..87031252-chr7:87041003..87044064,3	MCF-7	breast:
47	chr7:87138736..87139256-chr9:139980542..139981460,2	HCT-116	colon:
48	chr7:86568193..86568776-chr7:87081301..87082150,2	MCF-7	breast:
49	chr7:86940770..86949819-chr7:87040881..87047482,46	MCF-7	breast:
50	chr7:86942444..86943029-chr7:87045736..87046673,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CROT-1	chr7:87105081-87107196	NONHSAT121834

No data

Variant related genes	Relation type
ABCB1	TF binding region
ABCB4	TF binding region
ABCB1	CpG island
ABCB4	CpG island
ENSG00000177239	chromatin interactions
ENSG00000135164	chromatin interactions
ENSG00000135185	chromatin interactions
ENSG00000005471	chromatin interactions
ENSG00000005469	chromatin interactions
ENSG00000182165	chromatin interactions
ENSG00000268996	chromatin interactions
ENSG00000224046	chromatin interactions

Extended variants
information (count: 3371 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:3371 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs31659	chr7:87040629-87040630	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs45563233	chr7:87040650-87040651	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs185055455	chr7:87040706-87040707	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs568767633	chr7:87040775-87040776	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs550854173	chr7:87040786-87040787	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs189955633	chr7:87040796-87040797	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs149108707	chr7:87040825-87040826	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs569015628	chr7:87040907-87040908	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs533880303	chr7:87040921-87040922	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs536536738	chr7:87040965-87040966	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs566599395	chr7:87040993-87040994	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs533960000	chr7:87041001-87041002	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs371806200	chr7:87041117-87041118	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs17149542	chr7:87041144-87041145	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs570755181	chr7:87041149-87041150	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs537754815	chr7:87041162-87041163	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs45550235	chr7:87041184-87041185	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs8187805	chr7:87041185-87041186	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs575565764	chr7:87041234-87041235	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs121918440	chr7:87041264-87041265	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs61730509	chr7:87041333-87041334	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs201498350	chr7:87041361-87041362	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs573038020	chr7:87041377-87041378	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs368692582	chr7:87041399-87041400	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs372187960	chr7:87041400-87041401	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs565187074	chr7:87041420-87041421	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs577423887	chr7:87041422-87041423	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs544592566	chr7:87041437-87041438	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs562473167	chr7:87041522-87041523	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs45458995	chr7:87041557-87041558	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs181222840	chr7:87041576-87041577	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs560280155	chr7:87041597-87041598	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs185220555	chr7:87041678-87041679	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs552353941	chr7:87041729-87041730	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs189693339	chr7:87041750-87041751	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs538110230	chr7:87041765-87041766	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs549829677	chr7:87041766-87041767	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs553341768	chr7:87041789-87041790	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs375026828	chr7:87041816-87041817	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs45501791	chr7:87041848-87041849	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs11761050	chr7:87041856-87041857	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs140214930	chr7:87041910-87041911	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs45592439	chr7:87042023-87042024	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs558690892	chr7:87042100-87042101	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs180675311	chr7:87042139-87042140	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs116689990	chr7:87042194-87042195	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs563024356	chr7:87042271-87042272	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs575118060	chr7:87042344-87042345	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs35003464	chr7:87042352-87042353	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs534323919	chr7:87042382-87042383	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal adenocarcinoma	18820669	CNVD

Chromatin state (count:848 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86980000-87085600	Weak transcription	Right Ventricle	heart
2	chr7:86987000-87051800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr7:87019800-87079400	Strong transcription	Liver	Liver
4	chr7:87024800-87093200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:87026000-87043000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr7:87028800-87043600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:87034600-87051000	Weak transcription	Fetal Heart	heart
8	chr7:87037400-87064800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:87038000-87043800	Weak transcription	HepG2	liver
10	chr7:87039400-87045400	Weak transcription	Primary B cells from cord blood	blood
11	chr7:87040000-87040800	Enhancers	Aorta	Aorta
12	chr7:87040000-87041000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr7:87040000-87041000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:87040000-87044000	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr7:87040000-87044400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:87040000-87046000	Strong transcription	Primary B cells from peripheral blood	blood
17	chr7:87040200-87040800	Enhancers	Left Ventricle	heart
18	chr7:87040200-87040800	Enhancers	Psoas Muscle	Psoas
19	chr7:87040200-87041000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:87040200-87041000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr7:87040400-87043600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:87040600-87040800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:87040600-87041000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:87040600-87041000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr7:87040800-87044400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:87040800-87050400	Weak transcription	Left Ventricle	heart
27	chr7:87040800-87072400	Weak transcription	Aorta	Aorta
28	chr7:87040800-87085600	Weak transcription	Psoas Muscle	Psoas
29	chr7:87041000-87041800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr7:87041000-87042000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:87041000-87042200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:87041000-87042200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr7:87041000-87042400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:87041800-87042400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr7:87042000-87044600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:87042000-87044600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:87042200-87044600	Enhancers	NH-A	brain
38	chr7:87042200-87044800	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr7:87042200-87045600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:87042400-87042600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:87042400-87043800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr7:87042400-87044000	Enhancers	Hela-S3	cervix
43	chr7:87042600-87042800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:87042600-87043000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:87042600-87044400	Enhancers	Osteobl	bone
46	chr7:87042600-87044600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr7:87043000-87044000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:87043000-87044000	Enhancers	NHEK	skin
49	chr7:87043000-87044200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr7:87043000-87044600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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