Variant report

Variant	nsv831389
Chromosome Location	chr8:90575517-90753120
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1932)
CpG islands
(count:244)
Chromatin interactive
region (count:122)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1932 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90732814-90733099	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:90741133-90741702	K562	blood:	n/a	n/a
3	ARID3A	chr8:90629286-90629552	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:90738052-90738327	K562	blood:	n/a	n/a
5	ARID3A	chr8:90730496-90730904	K562	blood:	n/a	n/a
6	ARID3A	chr8:90623342-90624520	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:90742157-90742510	K562	blood:	n/a	n/a
8	ARID3A	chr8:90738074-90738343	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:90648425-90649121	HepG2	liver:	n/a	n/a
10	ATF1	chr8:90662407-90662935	K562	blood:	n/a	n/a
11	ATF1	chr8:90740926-90741719	K562	blood:	n/a	n/a
12	ATF1	chr8:90738051-90738334	K562	blood:	n/a	n/a
13	ATF2	chr8:90741233-90741894	GM12878	blood:	n/a	n/a
14	ATF2	chr8:90732722-90733233	GM12878	blood:	n/a	n/a
15	ATF2	chr8:90737929-90738551	GM12878	blood:	n/a	n/a
16	ATF2	chr8:90741953-90742740	GM12878	blood:	n/a	n/a
17	ATF2	chr8:90741207-90741815	GM12878	blood:	n/a	n/a
18	ATF2	chr8:90732595-90733323	GM12878	blood:	n/a	n/a
19	ATF2	chr8:90737920-90738636	GM12878	blood:	n/a	n/a
20	ATF2	chr8:90738026-90738427	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr8:90741902-90742786	GM12878	blood:	n/a	n/a
22	ATF3	chr8:90623916-90624492	A549	lung:	n/a	n/a
23	ATF3	chr8:90623655-90624566	HCT-116	colon:	n/a	n/a
24	BACH1	chr8:90738733-90738759	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:90738096-90738310	K562	blood:	n/a	n/a
26	BACH1	chr8:90623632-90623747	K562	blood:	n/a	n/a
27	BATF	chr8:90741449-90741737	GM12878	blood:	n/a	n/a
28	BATF	chr8:90738011-90738449	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
29	BATF	chr8:90598761-90598934	GM12878	blood:	n/a	n/a
30	BATF	chr8:90741444-90741729	GM12878	blood:	n/a	n/a
31	BATF	chr8:90738003-90738500	GM12878	blood:	n/a	chr8:90738291-90738302 chr8:90738292-90738302
32	BATF	chr8:90732830-90733137	GM12878	blood:	n/a	n/a
33	BATF	chr8:90742327-90742620	GM12878	blood:	n/a	n/a
34	BATF	chr8:90750493-90750763	GM12878	blood:	n/a	n/a
35	BATF	chr8:90742356-90742616	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:90741404-90741705	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:90591182-90591444	GM12878	blood:	n/a	n/a
38	BCL3	chr8:90623906-90624497	A549	lung:	n/a	chr8:90624090-90624099
39	BCL3	chr8:90732736-90733192	GM12878	blood:	n/a	n/a
40	BCL3	chr8:90623924-90624562	A549	lung:	n/a	chr8:90624090-90624099
41	BCL3	chr8:90737989-90738504	GM12878	blood:	n/a	chr8:90738122-90738131
42	BCL3	chr8:90624036-90624358	GM12878	blood:	n/a	chr8:90624090-90624099
43	BCLAF1	chr8:90737957-90738469	GM12878	blood:	n/a	chr8:90738122-90738131
44	BCLAF1	chr8:90737861-90738551	GM12878	blood:	n/a	chr8:90738122-90738131 chr8:90737903-90737912
45	BCLAF1	chr8:90742189-90742602	GM12878	blood:	n/a	chr8:90742261-90742270
46	BCLAF1	chr8:90741285-90741840	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:90738026-90738384	K562	blood:	n/a	n/a
48	BHLHE40	chr8:90740597-90740708	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:90623561-90624552	HepG2	liver:	n/a	n/a
50	BHLHE40	chr8:90733984-90734101	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90730638-90730688	PANC-1	pancreas:	n/a
2	chr8:90624127-90624177	Hepatocyte	liver:	n/a
3	chr8:90730638-90730688	GM12892	blood:	n/a
4	chr8:90577545-90577595	Hepatocyte	liver:	n/a
5	chr8:90730638-90730688	ovcar-3	ovarian:	n/a
6	chr8:90577545-90577595	HAEpiC	amniotic membrane:	n/a
7	chr8:90624127-90624177	HAEpiC	amniotic membrane:	n/a
8	chr8:90730638-90730688	AG04450	lung:	fetal
9	chr8:90730638-90730688	HRCEpiC	kidney:	n/a
10	chr8:90624127-90624177	K562	blood:	n/a
11	chr8:90636522-90636572	LNCaP	prostate:	n/a
12	chr8:90636522-90636572	IMR90	lung:	fetal
13	chr8:90624127-90624177	GM19239	blood:	n/a
14	chr8:90624127-90624177	IMR90	lung:	fetal
15	chr8:90577545-90577595	GM12878	blood:	n/a
16	chr8:90577545-90577595	H1-hESC	embryonic stem cell:	embryo
17	chr8:90624127-90624177	HepG2	liver:	n/a
18	chr8:90636522-90636572	HRE	kidney:	n/a
19	chr8:90624127-90624177	HL-60	blood:	n/a
20	chr8:90577545-90577595	HIPEpiC	eye:	n/a
21	chr8:90577545-90577595	AG09319	gingival:	n/a
22	chr8:90730638-90730688	Hepatocyte	liver:	n/a
23	chr8:90624127-90624177	Jurkat	blood:	n/a
24	chr8:90636522-90636572	BE2_C	brain:	n/a
25	chr8:90577545-90577595	SK-N-SH	brain:	n/a
26	chr8:90577545-90577595	ovcar-3	ovarian:	n/a
27	chr8:90730638-90730688	BJ	skin:	n/a
28	chr8:90624127-90624177	GM12892	blood:	n/a
29	chr8:90636522-90636572	NHDF-neo	bronchial:	n/a
30	chr8:90636522-90636572	PrEC	prostate:	n/a
31	chr8:90577545-90577595	HCT-116	colon:	n/a
32	chr8:90730638-90730688	SKMC	muscle:	n/a
33	chr8:90636522-90636572	SK-N-MC	brain:	n/a
34	chr8:90624127-90624177	U87	brain:	n/a
35	chr8:90624127-90624177	Caco-2	colon:	n/a
36	chr8:90624127-90624177	SAEC	small airway:	n/a
37	chr8:90577545-90577595	A549	lung:	n/a
38	chr8:90730638-90730688	IMR90	lung:	fetal
39	chr8:90636522-90636572	HepG2	liver:	n/a
40	chr8:90624127-90624177	NH-A	brain:	n/a
41	chr8:90577545-90577595	SAEC	small airway:	n/a
42	chr8:90577545-90577595	HNPCEpiC	eye:	n/a
43	chr8:90730638-90730688	HIPEpiC	eye:	n/a
44	chr8:90577545-90577595	PFSK-1	brain:	n/a
45	chr8:90636522-90636572	PFSK-1	brain:	n/a
46	chr8:90624127-90624177	AG09309	skin:	n/a
47	chr8:90730638-90730688	HCPEpiC	choroid plexus:	n/a
48	chr8:90577545-90577595	SKMC	muscle:	n/a
49	chr8:90624127-90624177	AG09319	gingival:	n/a
50	chr8:90624127-90624177	ProgFib	skin:	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:90714137..90717056-chr8:90737564..90740115,2	K562	blood:
2	chr8:90737819..90738602-chr8:90996411..90997232,4	MCF-7	breast:
3	chr17:65372095..65374964-chr8:90727575..90729422,2	MCF-7	breast:
4	chr8:90730418..90730960-chr8:90860233..90861169,2	MCF-7	breast:
5	chr8:90671410..90674363-chr8:90680458..90682126,2	K562	blood:
6	chr8:90271425..90272074-chr8:90701116..90702018,2	MCF-7	breast:
7	chr8:90627324..90629190-chr8:90732562..90735490,2	MCF-7	breast:
8	chr8:90664171..90665978-chr8:90667833..90669514,2	K562	blood:
9	chr8:90735006..90737562-chr8:90957378..90959199,2	MCF-7	breast:
10	chr8:90580330..90583016-chr8:90584267..90585810,2	MCF-7	breast:
11	chr8:90740621..90743258-chr8:90763138..90765800,2	K562	blood:
12	chr8:90730784..90732523-chr8:90913744..90915377,2	MCF-7	breast:
13	chr8:90497830..90499463-chr8:90622312..90625050,2	MCF-7	breast:
14	chr8:90658300..90660624-chr8:90699231..90701382,2	MCF-7	breast:
15	chr8:90730473..90731451-chr8:90996501..90997250,3	K562	blood:
16	chr8:90739799..90743850-chr8:90767861..90774313,11	K562	blood:
17	chr8:90576363..90578196-chr8:90582814..90584387,2	MCF-7	breast:
18	chr8:90707734..90710584-chr8:90712902..90714410,2	K562	blood:
19	chr8:90707735..90710054-chr8:90995310..90996868,2	MCF-7	breast:
20	chr8:90671410..90675466-chr8:90680458..90682318,3	K562	blood:
21	chr8:90741497..90743886-chr8:90913667..90916372,2	MCF-7	breast:
22	chr8:90727504..90729084-chr8:90996493..90998165,2	MCF-7	breast:
23	chr8:90727118..90729538-chr8:90730165..90731877,3	MCF-7	breast:
24	chr8:90740620..90742197-chr8:90743722..90745998,2	K562	blood:
25	chr8:90738830..90741040-chr8:90913929..90916655,2	K562	blood:
26	chr8:90638748..90641688-chr8:90643639..90646193,2	K562	blood:
27	chr8:90701576..90703155-chr8:90704849..90706858,2	K562	blood:
28	chr8:90677064..90679784-chr8:90680421..90682775,2	MCF-7	breast:
29	chr8:90707734..90710584-chr8:90712902..90714410,2	K562	blood:
30	chr8:90730369..90731173-chr8:91007945..91008879,2	K562	blood:
31	chr8:89930914..89931750-chr8:90701140..90701846,2	MCF-7	breast:
32	chr8:90750906..90752567-chr8:90769734..90771633,2	MCF-7	breast:
33	chr8:90617470..90619221-chr8:90620152..90623030,2	K562	blood:
34	chr8:90744912..90747575-chr8:90768585..90770314,2	MCF-7	breast:
35	chr8:90729414..90732733-chr8:91011369..91014401,3	MCF-7	breast:
36	chr8:90579098..90579926-chr8:90624854..90625740,2	MCF-7	breast:
37	chr8:90701508..90704091-chr8:90704725..90706436,2	MCF-7	breast:
38	chr8:90664171..90665978-chr8:90667833..90669514,2	K562	blood:
39	chr8:90633001..90635193-chr8:90639788..90641553,2	MCF-7	breast:
40	chr8:90737750..90738653-chr8:90995891..90997375,11	MCF-7	breast:
41	chr8:90734885..90744209-chr8:90767977..90774247,14	MCF-7	breast:
42	chr8:90737820..90738670-chr8:90996630..90997353,4	K562	blood:
43	chr8:90737934..90739593-chr8:90739830..90742161,2	K562	blood:
44	chr8:90576363..90578196-chr8:90582814..90584387,2	MCF-7	breast:
45	chr8:87715292..87715843-chr8:90701514..90702072,2	K562	blood:
46	chr8:90580330..90583016-chr8:90584267..90585810,2	MCF-7	breast:
47	chr8:90617470..90619221-chr8:90620152..90623030,2	K562	blood:
48	chr8:90737986..90738708-chr8:90849422..90850036,2	MCF-7	breast:
49	chr8:90265298..90266142-chr8:90701378..90702003,2	MCF-7	breast:
50	chr8:90732834..90736227-chr8:90736670..90741646,5	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-1	chr8:90621629-90621723	ENSG00000251136
2	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136
3	lnc-NBN-1	chr8:90734243-90734578	ENSG00000251136
4	lnc-NBN-1	chr8:90641382-90641499	ENSG00000251136
5	lnc-NBN-1	chr8:90635314-90635433	ENSG00000251136
6	lnc-NBN-1	chr8:90621638-90621723	ENSG00000251136.4
7	lnc-NBN-1	chr8:90736857-90737194	ENSG00000251136
8	lnc-NBN-1	chr8:90729656-90729956	ENSG00000251136
9	lnc-NBN-1	chr8:90629308-90629386	ENSG00000251136
10	lnc-NBN-1	chr8:90624013-90624218	ENSG00000251136.4
11	lnc-NBN-1	chr8:90623663-90623699	ENSG00000251136.4
12	lnc-NBN-1	chr8:90640384-90640528	ENSG00000251136
13	lnc-NBN-1	chr8:90729627-90733428	ENSG00000251136
14	lnc-NBN-1	chr8:90627412-90627568	NONHSAT127613
15	lnc-RIPK2-2	chr8:90627189-90627723	NONHSAT127614
16	lnc-NBN-1	chr8:90737746-90737869	ENSG00000251136
17	lnc-NBN-1	chr8:90623631-90624218	NONHSAT127613
18	lnc-NBN-1	chr8:90732820-90733604	NONHSAT127622
19	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136
20	lnc-NBN-1	chr8:90623663-90623699	ENSG00000251136
21	lnc-NBN-1	chr8:90735244-90735764	NONHSAT127622
22	lnc-NBN-1	chr8:90632912-90633104	ENSG00000251136
23	lnc-NBN-1	chr8:90629158-90629385	ENSG00000251136
24	lnc-NBN-1	chr8:90608315-90608741	NONHSAT127610
25	lnc-NBN-1	chr8:90734243-90734384	ENSG00000251136
26	lnc-NBN-1	chr8:90736857-90737194	NONHSAT127622
27	lnc-NBN-1	chr8:90629222-90629385	ENSG00000251136
28	lnc-NBN-1	chr8:90733132-90733602	ENSG00000251136
29	lnc-NBN-1	chr8:90624013-90624218	ENSG00000251136
30	lnc-NBN-1	chr8:90736857-90737158	ENSG00000251136
31	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136.4
32	lnc-NBN-1	chr8:90733172-90733602	ENSG00000251136
33	lnc-NBN-1	chr8:90640384-90640528	ENSG00000251136.4
34	lnc-NBN-1	chr8:90734243-90734384	ENSG00000251136
35	lnc-NBN-1	chr8:90623585-90624218	ENSG00000251136
36	lnc-NBN-1	chr8:90734243-90734578	NONHSAT127622
37	lnc-NBN-1	chr8:90737746-90737871	NONHSAT127622
38	lnc-NBN-1	chr8:90641382-90641499	ENSG00000251136.4

No data

Variant related genes	Relation type
ENSG00000251136	TF binding region
ENSG00000251136	CpG island
ENSG00000104312	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000154217	chromatin interactions
ENSG00000104320	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000207359	chromatin interactions
ENSG00000164823	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000201801	chromatin interactions
HMGA2	miRNA target sites
CLN6	miRNA target sites
RGPD6	miRNA target sites
HIPK3	miRNA target sites
TMEM214	miRNA target sites
DPH1	miRNA target sites
EIF4G3	miRNA target sites
HNF4A	miRNA target sites
MORF4L2	miRNA target sites
BCL2	miRNA target sites
MFHAS1	miRNA target sites
EIF2C1	miRNA target sites
HNRNPD	miRNA target sites
NCOA3	miRNA target sites
CADM1	miRNA target sites
TPM3	miRNA target sites
KLK6	miRNA target sites
NAPEPLD	miRNA target sites

Extended variants
information (count: 6661 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:6661 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577317465	chr8:90575565-90575566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541530621	chr8:90575575-90575576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559821394	chr8:90575840-90575841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193040670	chr8:90575956-90575957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185787028	chr8:90575996-90575997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561251912	chr8:90576011-90576012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531466335	chr8:90576012-90576013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543648710	chr8:90576014-90576015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564922489	chr8:90576030-90576031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150678984	chr8:90576055-90576056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547067289	chr8:90576120-90576121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565407572	chr8:90576181-90576182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529654917	chr8:90576214-90576215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547740360	chr8:90576243-90576244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189121424	chr8:90576255-90576256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537343647	chr8:90576276-90576277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559148810	chr8:90576332-90576333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114192281	chr8:90576370-90576371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191452323	chr8:90576422-90576423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553533119	chr8:90576436-90576437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553526519	chr8:90576449-90576450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183983620	chr8:90576486-90576487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140130947	chr8:90576605-90576606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1510465	chr8:90576635-90576636	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559730114	chr8:90576657-90576658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188369256	chr8:90576662-90576663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377024637	chr8:90576726-90576727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543335591	chr8:90576737-90576738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565116184	chr8:90576761-90576762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532195328	chr8:90576763-90576764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540791289	chr8:90576822-90576823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559029783	chr8:90576843-90576844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529691757	chr8:90576892-90576893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78081476	chr8:90576904-90576905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10081423	chr8:90576918-90576919	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs4960975	chr8:90576922-90576923	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs78365676	chr8:90576928-90576929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199714129	chr8:90577006-90577007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200254925	chr8:90577048-90577049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535249321	chr8:90577058-90577059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71528721	chr8:90577095-90577096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181236615	chr8:90577096-90577097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535943437	chr8:90577110-90577111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186603224	chr8:90577230-90577231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368545664	chr8:90577275-90577276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146820673	chr8:90577315-90577316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546149217	chr8:90577352-90577353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78310012	chr8:90577375-90577376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576683503	chr8:90577380-90577381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140583051	chr8:90577410-90577411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

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
Bipolar disorder	19114987	CNVD

Chromatin state (count:1208 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90572800-90579800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:90573600-90576600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:90573800-90575800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:90573800-90576400	Enhancers	HMEC	breast
5	chr8:90574400-90576600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:90574600-90576200	Enhancers	NHEK	skin
7	chr8:90574600-90576600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:90574800-90575600	Enhancers	Osteobl	bone
9	chr8:90574800-90575800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:90574800-90576200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:90574800-90576200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:90574800-90576400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:90575200-90576400	Enhancers	NHDF-Ad	bronchial
14	chr8:90575400-90576600	Enhancers	Dnd41	blood
15	chr8:90575400-90576800	Enhancers	HUVEC	blood vessel
16	chr8:90575800-90577600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr8:90576000-90576400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr8:90576000-90576400	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr8:90576200-90579800	Weak transcription	NHEK	skin
20	chr8:90576400-90577600	Weak transcription	HMEC	breast
21	chr8:90576400-90577600	Weak transcription	NHDF-Ad	bronchial
22	chr8:90576400-90577800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:90576600-90577600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:90576600-90577600	Weak transcription	Dnd41	blood
25	chr8:90576600-90577800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr8:90576600-90578400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:90576800-90577000	Enhancers	Aorta	Aorta
28	chr8:90576800-90577800	Weak transcription	HUVEC	blood vessel
29	chr8:90577000-90578400	Weak transcription	Aorta	Aorta
30	chr8:90577600-90578000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr8:90577600-90578000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:90577600-90578200	Enhancers	Dnd41	blood
33	chr8:90577600-90581000	Enhancers	HMEC	breast
34	chr8:90577800-90578000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:90577800-90578000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr8:90577800-90578000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:90577800-90578000	Enhancers	HUVEC	blood vessel
38	chr8:90577800-90578000	Enhancers	NHDF-Ad	bronchial
39	chr8:90577800-90578600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr8:90578000-90578200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:90578400-90578600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:90578600-90579000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr8:90579000-90582600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:90579600-90579800	Enhancers	Hela-S3	cervix
45	chr8:90579800-90580000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:90579800-90580400	Enhancers	NHEK	skin
47	chr8:90580000-90580200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:90580400-90580600	Enhancers	Right Ventricle	heart
49	chr8:90581000-90581400	Weak transcription	HMEC	breast
50	chr8:90581400-90581800	Enhancers	HMEC	breast

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