Variant report

Variant	nsv891180
Chromosome Location	chr8:90697810-90802491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2283)
CpG islands
(count:915)
Chromatin interactive
region (count:181)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2283 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90764699-90764838	K562	blood:	n/a	n/a
2	ARID3A	chr8:90742157-90742510	K562	blood:	n/a	n/a
3	ARID3A	chr8:90730496-90730904	K562	blood:	n/a	n/a
4	ARID3A	chr8:90741133-90741702	K562	blood:	n/a	n/a
5	ARID3A	chr8:90771089-90771807	K562	blood:	n/a	n/a
6	ARID3A	chr8:90738074-90738343	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:90769008-90770155	HepG2	liver:	n/a	chr8:90769078-90769094 chr8:90769079-90769095
8	ARID3A	chr8:90771385-90771852	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:90769903-90770210	K562	blood:	n/a	n/a
10	ARID3A	chr8:90759504-90759576	K562	blood:	n/a	n/a
11	ARID3A	chr8:90774096-90774394	K562	blood:	n/a	n/a
12	ARID3A	chr8:90738052-90738327	K562	blood:	n/a	n/a
13	ARID3A	chr8:90770453-90770466	K562	blood:	n/a	n/a
14	ARID3A	chr8:90732814-90733099	HepG2	liver:	n/a	n/a
15	ATF1	chr8:90740926-90741719	K562	blood:	n/a	n/a
16	ATF1	chr8:90769749-90770229	K562	blood:	n/a	n/a
17	ATF1	chr8:90738051-90738334	K562	blood:	n/a	n/a
18	ATF1	chr8:90767992-90768547	K562	blood:	n/a	n/a
19	ATF1	chr8:90771400-90771928	K562	blood:	n/a	n/a
20	ATF1	chr8:90796935-90797378	K562	blood:	n/a	n/a
21	ATF2	chr8:90775737-90776232	GM12878	blood:	n/a	n/a
22	ATF2	chr8:90732722-90733233	GM12878	blood:	n/a	n/a
23	ATF2	chr8:90775723-90776138	GM12878	blood:	n/a	n/a
24	ATF2	chr8:90769494-90770311	GM12878	blood:	n/a	chr8:90769943-90769954
25	ATF2	chr8:90769222-90770228	GM12878	blood:	n/a	chr8:90769943-90769954
26	ATF2	chr8:90769515-90770240	H1-hESC	embryonic stem cell:	n/a	chr8:90769943-90769954
27	ATF2	chr8:90741953-90742740	GM12878	blood:	n/a	n/a
28	ATF2	chr8:90732595-90733323	GM12878	blood:	n/a	n/a
29	ATF2	chr8:90741233-90741894	GM12878	blood:	n/a	n/a
30	ATF2	chr8:90769317-90770206	H1-hESC	embryonic stem cell:	n/a	chr8:90769943-90769954
31	ATF2	chr8:90741207-90741815	GM12878	blood:	n/a	n/a
32	ATF2	chr8:90737929-90738551	GM12878	blood:	n/a	n/a
33	ATF2	chr8:90737920-90738636	GM12878	blood:	n/a	n/a
34	ATF2	chr8:90738026-90738427	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr8:90741902-90742786	GM12878	blood:	n/a	n/a
36	ATF3	chr8:90769734-90770144	K562	blood:	n/a	chr8:90769942-90769955 chr8:90770002-90770011 chr8:90769943-90769954 chr8:90769941-90769954 chr8:90769942-90769955 chr8:90769943-90769954 chr8:90769942-90769952
37	BACH1	chr8:90738733-90738759	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr8:90785178-90785244	K562	blood:	n/a	n/a
39	BACH1	chr8:90738096-90738310	K562	blood:	n/a	n/a
40	BACH1	chr8:90769365-90769405	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr8:90769706-90770584	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr8:90732830-90733137	GM12878	blood:	n/a	n/a
43	BATF	chr8:90738011-90738449	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
44	BATF	chr8:90775761-90776188	GM12878	blood:	n/a	n/a
45	BATF	chr8:90742327-90742620	GM12878	blood:	n/a	n/a
46	BATF	chr8:90777999-90778329	GM12878	blood:	n/a	n/a
47	BATF	chr8:90775856-90776161	GM12878	blood:	n/a	n/a
48	BATF	chr8:90750493-90750763	GM12878	blood:	n/a	n/a
49	BATF	chr8:90794451-90794806	GM12878	blood:	n/a	n/a
50	BATF	chr8:90742356-90742616	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90772386-90772436	ECC-1	luminal epithelium:	n/a
2	chr8:90770146-90770196	SAEC	small airway:	n/a
3	chr8:90794647-90794697	GM19239	blood:	n/a
4	chr8:90766731-90766781	Caco-2	colon:	n/a
5	chr8:90769570-90769620	ECC-1	luminal epithelium:	n/a
6	chr8:90769570-90769620	IMR90	lung:	fetal
7	chr8:90772386-90772436	AG04450	lung:	fetal
8	chr8:90770219-90770269	SAEC	small airway:	n/a
9	chr8:90730638-90730688	GM12878	blood:	n/a
10	chr8:90769512-90769562	SK-N-SH	brain:	n/a
11	chr8:90730638-90730688	AG10803	skin:	n/a
12	chr8:90769698-90769748	PrEC	prostate:	n/a
13	chr8:90770146-90770196	GM06990	blood:	n/a
14	chr8:90770219-90770269	GM12891	blood:	n/a
15	chr8:90769710-90769760	LNCaP	prostate:	n/a
16	chr8:90766731-90766781	AoSMC	blood vessel:	n/a
17	chr8:90769545-90769595	T-47D	breast:	n/a
18	chr8:90769698-90769748	ProgFib	skin:	n/a
19	chr8:90770146-90770196	GM12892	blood:	n/a
20	chr8:90769570-90769620	NT2-D1	testis:	n/a
21	chr8:90770146-90770196	HL-60	blood:	n/a
22	chr8:90769512-90769562	H1-hESC	embryonic stem cell:	embryo
23	chr8:90769570-90769620	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:90730638-90730688	K562	blood:	n/a
25	chr8:90770146-90770196	Jurkat	blood:	n/a
26	chr8:90770456-90770506	AG04449	skin:	fetal
27	chr8:90784993-90785043	SK-N-SH_RA	brain:	n/a
28	chr8:90794647-90794697	ovcar-3	ovarian:	n/a
29	chr8:90769698-90769748	HCF	heart:	n/a
30	chr8:90770146-90770196	SK-N-MC	brain:	n/a
31	chr8:90784993-90785043	HRCEpiC	kidney:	n/a
32	chr8:90770456-90770506	HRPEpiC	eye:	n/a
33	chr8:90730638-90730688	PANC-1	pancreas:	n/a
34	chr8:90794647-90794697	H1-hESC	embryonic stem cell:	embryo
35	chr8:90769545-90769595	HRPEpiC	eye:	n/a
36	chr8:90769512-90769562	HCT-116	colon:	n/a
37	chr8:90730638-90730688	Hela-S3	cervix:	n/a
38	chr8:90794647-90794697	K562	blood:	n/a
39	chr8:90770219-90770269	NH-A	brain:	n/a
40	chr8:90769710-90769760	BJ	skin:	n/a
41	chr8:90772862-90772912	HEEpiC	esophagus:	n/a
42	chr8:90776474-90776524	AG04449	skin:	fetal
43	chr8:90730638-90730688	GM06990	blood:	n/a
44	chr8:90772862-90772912	SKMC	muscle:	n/a
45	chr8:90772862-90772912	HCF	heart:	n/a
46	chr8:90769545-90769595	AG09309	skin:	n/a
47	chr8:90769512-90769562	GM06990	blood:	n/a
48	chr8:90766731-90766781	GM12892	blood:	n/a
49	chr8:90766731-90766781	RPTEC	kidney:	n/a
50	chr8:90769545-90769595	NHDF-neo	bronchial:	n/a

(count:181 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:90730992..90732620-chr8:90854047..90856090,2	MCF-7	breast:
2	chr8:90730221..90731273-chr8:91007539..91008842,5	MCF-7	breast:
3	chr8:90752983..90756516-chr8:90768798..90771360,4	MCF-7	breast:
4	chr8:90770923..90772478-chr8:91013915..91015881,2	K562	blood:
5	chr8:90769811..90771678-chr8:91656094..91659219,3	MCF-7	breast:
6	chr8:90776459..90778873-chr8:90786925..90789865,2	K562	blood:
7	chr8:90756480..90757980-chr8:90764220..90765823,2	K562	blood:
8	chr8:90753685..90756450-chr8:90766720..90768459,2	MCF-7	breast:
9	chr8:90756480..90757980-chr8:90764220..90765823,2	K562	blood:
10	chr8:90735006..90737562-chr8:90957378..90959199,2	MCF-7	breast:
11	chr1:152113868..152114505-chr8:90798777..90799465,2	MCF-7	breast:
12	chr8:90775597..90777487-chr8:90778142..90780568,2	K562	blood:
13	chr8:90775597..90777487-chr8:90778142..90780568,2	K562	blood:
14	chr8:90737773..90739680-chr8:90867503..90870182,2	MCF-7	breast:
15	chr8:90265298..90266142-chr8:90701378..90702003,2	MCF-7	breast:
16	chr8:90770081..90772255-chr8:90988919..90991592,2	MCF-7	breast:
17	chr8:90791710..90793758-chr8:90796402..90798815,3	MCF-7	breast:
18	chr8:90800222..90801982-chr8:90840675..90842723,2	MCF-7	breast:
19	chr8:90735002..90740593-chr8:90994599..90998168,11	MCF-7	breast:
20	chr8:90737934..90739593-chr8:90739830..90742161,2	K562	blood:
21	chr8:90801418..90803391-chr8:90808526..90811319,2	MCF-7	breast:
22	chr8:90782135..90784385-chr8:90789224..90791497,2	K562	blood:
23	chr8:90788699..90792573-chr8:90996217..90998925,4	MCF-7	breast:
24	chr8:90790967..90797055-chr8:90994383..90998113,5	MCF-7	breast:
25	chr8:90768498..90770140-chr8:90791646..90793949,2	MCF-7	breast:
26	chr11:62608642..62609306-chr8:90769761..90770422,2	HCT-116	colon:
27	chr8:90775966..90778463-chr8:90780267..90782442,2	K562	blood:
28	chr8:90767933..90770718-chr8:90788442..90790406,2	K562	blood:
29	chr8:90769927..90772219-chr8:90802189..90804618,2	MCF-7	breast:
30	chr8:90734885..90744209-chr8:90767977..90774247,14	MCF-7	breast:
31	chr8:90791423..90793075-chr8:90800712..90802481,2	MCF-7	breast:
32	chr8:90714137..90717056-chr8:90737564..90740115,2	K562	blood:
33	chr8:90779049..90780905-chr8:90790813..90793376,2	MCF-7	breast:
34	chr8:90788241..90790215-chr8:90796193..90798741,2	K562	blood:
35	chr11:35684171..35684725-chr8:90769468..90770126,2	Hela-S3	cervix:
36	chr17:65372095..65374964-chr8:90727575..90729422,2	MCF-7	breast:
37	chr8:89930914..89931750-chr8:90701140..90701846,2	MCF-7	breast:
38	chr8:90772791..90774637-chr8:90794290..90797972,3	MCF-7	breast:
39	chr8:90772791..90774637-chr8:90794290..90797972,3	MCF-7	breast:
40	chr8:90776459..90778873-chr8:90786925..90789865,2	K562	blood:
41	chr5:170814542..170815123-chr8:90769919..90770441,2	HCT-116	colon:
42	chr8:90750906..90752567-chr8:90769734..90771633,2	MCF-7	breast:
43	chr8:90775245..90777466-chr8:90780625..90782442,2	K562	blood:
44	chr8:90727781..90733734-chr8:90995200..90998684,11	MCF-7	breast:
45	chr8:90794527..90798218-chr8:90801291..90805045,3	K562	blood:
46	chr8:90737750..90738653-chr8:90995891..90997375,11	MCF-7	breast:
47	chr8:90742416..90744281-chr8:90745142..90746926,3	MCF-7	breast:
48	chr8:90787718..90790073-chr8:90792204..90794222,2	K562	blood:
49	chr8:90787120..90788718-chr8:90790537..90792123,2	K562	blood:
50	chr8:90737986..90738708-chr8:90849422..90850036,2	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-1	chr8:90737746-90737871	NONHSAT127622
2	lnc-NBN-5	chr8:90798778-90799078	ucscGeneNc_uc003yed_1
3	lnc-NBN-1	chr8:90769273-90769946	NONHSAT127610
4	lnc-NBN-1	chr8:90733132-90733602	ENSG00000251136
5	lnc-NBN-1	chr8:90729627-90733428	ENSG00000251136
6	lnc-NBN-1	chr8:90734243-90734578	ENSG00000251136
7	lnc-NBN-1	chr8:90769273-90769955	ENSG00000251136
8	lnc-NBN-1	chr8:90729656-90729956	ENSG00000251136
9	lnc-NBN-1	chr8:90769273-90769939	ENSG00000251136
10	lnc-NBN-1	chr8:90734243-90734578	NONHSAT127622
11	lnc-NBN-1	chr8:90768463-90768838	ENSG00000251136
12	lnc-OSGIN2-3	chr8:90792599-90793006	NONHSAT127627
13	lnc-NBN-1	chr8:90769273-90769955	ENSG00000251136.4
14	lnc-NBN-1	chr8:90737746-90737869	ENSG00000251136
15	lnc-NBN-1	chr8:90734243-90734384	ENSG00000251136
16	lnc-NBN-1	chr8:90734243-90734384	ENSG00000251136
17	lnc-NBN-1	chr8:90733172-90733602	ENSG00000251136
18	lnc-NBN-1	chr8:90732820-90733604	NONHSAT127622
19	lnc-NBN-1	chr8:90736857-90737194	ENSG00000251136
20	lnc-NBN-1	chr8:90736857-90737158	ENSG00000251136
21	lnc-NBN-1	chr8:90735244-90735764	NONHSAT127622
22	lnc-NBN-1	chr8:90736857-90737194	NONHSAT127622
23	lnc-OSGIN2-3	chr8:90792316-90792388	NONHSAT127627
24	lnc-NBN-1	chr8:90769273-90769592	ENSG00000251136

No data

Variant related genes	Relation type
ENSG00000251136	TF binding region
RIPK2	TF binding region
ENSG00000251136	CpG island
RIPK2	CpG island
ENSG00000251136	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000253744	chromatin interactions
ENSG00000003393	chromatin interactions
ENSG00000247363	chromatin interactions
ENSG00000104312	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000174886	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000116001	chromatin interactions
ENSG00000180694	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000246792	chromatin interactions
ENSG00000166326	chromatin interactions
ENSG00000166439	chromatin interactions
ENSG00000153914	chromatin interactions
ENSG00000207359	chromatin interactions
ENSG00000164823	chromatin interactions
ENSG00000154217	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000115998	chromatin interactions
ENSG00000104320	chromatin interactions
ENSG00000181163	chromatin interactions
ENSG00000111581	chromatin interactions
ENSG00000127947	chromatin interactions
ENSG00000163689	chromatin interactions
ENSG00000267740	chromatin interactions
GPD1L	miRNA target sites
UCP2	miRNA target sites
DPH1	miRNA target sites
TNFRSF10B	miRNA target sites
RGPD6	miRNA target sites
KLK6	miRNA target sites
GPD2	miRNA target sites
HMGA2	miRNA target sites
CADM1	miRNA target sites
TPM3	miRNA target sites
TBRG1	miRNA target sites
TMEM214	miRNA target sites
BCL2	miRNA target sites

Extended variants
information (count: 3854 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:3854 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs218892	chr8:90697810-90697811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181278696	chr8:90697811-90697812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568492249	chr8:90697812-90697813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115276490	chr8:90697831-90697832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4961158	chr8:90697835-90697836	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs73291843	chr8:90697954-90697955	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs568020211	chr8:90697970-90697971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs60311737	chr8:90698010-90698011	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs550967268	chr8:90698040-90698041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542900549	chr8:90698051-90698052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185531145	chr8:90698087-90698088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548986184	chr8:90698094-90698095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569451298	chr8:90698095-90698096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539631759	chr8:90698112-90698113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577466354	chr8:90698113-90698114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56405377	chr8:90698148-90698149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs533986308	chr8:90698173-90698174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147614102	chr8:90698215-90698216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534862928	chr8:90698216-90698217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13278061	chr8:90698260-90698261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs190294730	chr8:90698273-90698274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182927228	chr8:90698275-90698276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545677913	chr8:90698285-90698286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564211080	chr8:90698294-90698295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574980115	chr8:90698334-90698335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139544719	chr8:90698438-90698439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546672704	chr8:90698469-90698470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149695439	chr8:90698478-90698479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563805650	chr8:90698496-90698497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576103160	chr8:90698530-90698531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528863391	chr8:90698540-90698541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551292946	chr8:90698552-90698553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569429903	chr8:90698556-90698557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540062267	chr8:90698645-90698646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575675920	chr8:90698646-90698647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551688923	chr8:90698661-90698662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546243454	chr8:90698698-90698699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566675046	chr8:90698719-90698720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534046700	chr8:90698720-90698721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564179602	chr8:90698883-90698884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79531170	chr8:90698889-90698890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34093014	chr8:90698913-90698914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113713977	chr8:90698936-90698937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546620434	chr8:90698947-90698948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114394675	chr8:90698978-90698979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191909043	chr8:90698979-90698980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575440111	chr8:90698999-90699000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574513296	chr8:90699041-90699042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546038943	chr8:90699080-90699081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34038516	chr8:90699121-90699122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:107)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2621 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90693200-90715600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:90703800-90704400	Enhancers	NH-A	brain
3	chr8:90704000-90704200	Enhancers	A549	lung
4	chr8:90704000-90704400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr8:90704400-90709600	Weak transcription	NH-A	brain
6	chr8:90709000-90720200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:90709400-90709600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr8:90709600-90709800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:90709600-90710200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:90709600-90710200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr8:90709600-90710200	Enhancers	Adipose Nuclei	Adipose
12	chr8:90709600-90710200	Enhancers	A549	lung
13	chr8:90709600-90710200	Enhancers	Hela-S3	cervix
14	chr8:90709600-90710200	Enhancers	NH-A	brain
15	chr8:90709600-90710200	Enhancers	Osteobl	bone
16	chr8:90709800-90710000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:90709800-90710000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr8:90709800-90710000	Enhancers	HSMMtube	muscle
19	chr8:90709800-90710200	Enhancers	NHEK	skin
20	chr8:90709800-90710600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:90710000-90710200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr8:90710000-90710200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:90710000-90716200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:90710000-90730000	Weak transcription	HSMMtube	muscle
25	chr8:90710200-90715800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr8:90710200-90716400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr8:90710200-90729600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr8:90710200-90730400	Weak transcription	A549	lung
29	chr8:90710200-90731200	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr8:90710200-90736200	Weak transcription	Adipose Nuclei	Adipose
31	chr8:90710600-90715800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:90711200-90715400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:90711200-90733800	Weak transcription	Brain Cingulate Gyrus	brain
34	chr8:90711400-90712800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr8:90711400-90720200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr8:90712200-90713000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:90712200-90715600	Weak transcription	Aorta	Aorta
38	chr8:90712400-90712800	Enhancers	K562	blood
39	chr8:90712600-90713200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:90712800-90713200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr8:90712800-90713200	Enhancers	Spleen	Spleen
42	chr8:90712800-90713400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr8:90713000-90713200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr8:90713000-90713200	Enhancers	Left Ventricle	heart
45	chr8:90713200-90713400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr8:90713200-90714200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:90713200-90715400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr8:90713200-90716400	Weak transcription	Spleen	Spleen
49	chr8:90713200-90717600	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr8:90713200-90741200	Weak transcription	Left Ventricle	heart

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