Variant report

Variant	nsv468632
Chromosome Location	chr11:71200320-71289089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:996)
CpG islands
(count:3418)
Chromatin interactive
region (count:55)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71246189-71246536	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:71237205-71237575	HepG2	liver:	n/a	n/a
3	ATF1	chr11:71274374-71274763	K562	blood:	n/a	n/a
4	ATF2	chr11:71251016-71252199	GM12878	blood:	n/a	n/a
5	ATF2	chr11:71241553-71242059	GM12878	blood:	n/a	n/a
6	ATF2	chr11:71262610-71263131	GM12878	blood:	n/a	n/a
7	ATF2	chr11:71200262-71200721	GM12878	blood:	n/a	n/a
8	ATF2	chr11:71251026-71251407	GM12878	blood:	n/a	n/a
9	ATF2	chr11:71251483-71252131	GM12878	blood:	n/a	n/a
10	ATF2	chr11:71254369-71254678	GM12878	blood:	n/a	n/a
11	ATF2	chr11:71254252-71254755	GM12878	blood:	n/a	n/a
12	BACH1	chr11:71262761-71263011	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:71262748-71263014	K562	blood:	n/a	n/a
14	BACH1	chr11:71215809-71215924	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr11:71233426-71233787	GM12878	blood:	n/a	n/a
16	BATF	chr11:71251039-71251366	GM12878	blood:	n/a	n/a
17	BATF	chr11:71262740-71263045	GM12878	blood:	n/a	chr11:71262880-71262891
18	BATF	chr11:71250991-71251419	GM12878	blood:	n/a	n/a
19	BATF	chr11:71254317-71254656	GM12878	blood:	n/a	n/a
20	BATF	chr11:71262648-71263064	GM12878	blood:	n/a	chr11:71262880-71262891
21	BATF	chr11:71254310-71254769	GM12878	blood:	n/a	n/a
22	BATF	chr11:71200324-71200707	GM12878	blood:	n/a	chr11:71200539-71200550
23	BATF	chr11:71251533-71252059	GM12878	blood:	n/a	n/a
24	BCL11A	chr11:71232888-71233579	GM12878	blood:	n/a	n/a
25	BCL11A	chr11:71241675-71242012	GM12878	blood:	n/a	n/a
26	BCL11A	chr11:71233291-71233530	GM12878	blood:	n/a	n/a
27	BCL3	chr11:71288393-71289155	GM12878	blood:	n/a	n/a
28	BCL3	chr11:71267088-71267530	GM12878	blood:	n/a	n/a
29	BCL3	chr11:71288357-71289171	GM12878	blood:	n/a	n/a
30	BCL3	chr11:71281522-71282063	GM12878	blood:	n/a	n/a
31	BCL3	chr11:71281541-71282202	GM12878	blood:	n/a	n/a
32	BCL3	chr11:71251547-71252137	GM12878	blood:	n/a	n/a
33	BCLAF1	chr11:71241632-71241998	GM12878	blood:	n/a	n/a
34	BCLAF1	chr11:71251510-71252067	GM12878	blood:	n/a	n/a
35	BCLAF1	chr11:71250921-71251422	GM12878	blood:	n/a	chr11:71251210-71251219
36	BCLAF1	chr11:71251487-71252042	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:71251666-71251812	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:71246155-71246217	K562	blood:	n/a	n/a
39	BHLHE40	chr11:71274540-71274790	GM12878	blood:	n/a	n/a
40	BHLHE40	chr11:71254944-71255240	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:71242536-71242718	K562	blood:	n/a	n/a
42	BHLHE40	chr11:71200401-71200653	GM12878	blood:	n/a	n/a
43	BHLHE40	chr11:71251215-71251234	GM12878	blood:	n/a	n/a
44	BRCA1	chr11:71211677-71211892	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr11:71274467-71274725	HepG2	liver:	n/a	n/a
46	CEBPB	chr11:71267943-71268156	IMR90	lung:	n/a	n/a
47	CEBPB	chr11:71243021-71243338	K562	blood:	n/a	chr11:71243155-71243166
48	CEBPB	chr11:71215097-71215297	HepG2	liver:	n/a	n/a
49	CEBPB	chr11:71200388-71200792	IMR90	lung:	n/a	n/a
50	CEBPB	chr11:71211623-71211889	Hela-S3	cervix:	n/a	n/a

(count:3418 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71285546-71285596	NHBE	bronchial:	n/a
2	chr11:71230174-71230224	BJ	skin:	n/a
3	chr11:71285546-71285596	NHBE	bronchial:	n/a
4	chr11:71230174-71230224	BJ	skin:	n/a
5	chr11:71258392-71258442	RPTEC	kidney:	n/a
6	chr11:71248906-71248956	HNPCEpiC	eye:	n/a
7	chr11:71249212-71249262	HMEC	breast:	n/a
8	chr11:71202329-71202379	LNCaP	prostate:	n/a
9	chr11:71258917-71258967	AG10803	skin:	n/a
10	chr11:71202368-71202418	PANC-1	pancreas:	n/a
11	chr11:71287919-71287969	GM12892	blood:	n/a
12	chr11:71258392-71258442	HepG2	liver:	n/a
13	chr11:71235111-71235161	PANC-1	pancreas:	n/a
14	chr11:71258392-71258442	HNPCEpiC	eye:	n/a
15	chr11:71215361-71215411	K562	blood:	n/a
16	chr11:71258917-71258967	NH-A	brain:	n/a
17	chr11:71237650-71237700	SK-N-SH_RA	brain:	n/a
18	chr11:71239055-71239105	HAEpiC	amniotic membrane:	n/a
19	chr11:71259341-71259391	LNCaP	prostate:	n/a
20	chr11:71250073-71250123	AoSMC	blood vessel:	n/a
21	chr11:71202719-71202769	ProgFib	skin:	n/a
22	chr11:71235111-71235161	HEEpiC	esophagus:	n/a
23	chr11:71237650-71237700	AoSMC	blood vessel:	n/a
24	chr11:71259581-71259631	K562	blood:	n/a
25	chr11:71229988-71230038	BJ	skin:	n/a
26	chr11:71230734-71230784	SK-N-MC	brain:	n/a
27	chr11:71238270-71238320	ECC-1	luminal epithelium:	n/a
28	chr11:71202368-71202418	HCPEpiC	choroid plexus:	n/a
29	chr11:71258392-71258442	NT2-D1	testis:	n/a
30	chr11:71247746-71247796	SKMC	muscle:	n/a
31	chr11:71259341-71259391	AG09319	gingival:	n/a
32	chr11:71258392-71258442	HRCEpiC	kidney:	n/a
33	chr11:71275784-71275834	T-47D	breast:	n/a
34	chr11:71260323-71260373	RPTEC	kidney:	n/a
35	chr11:71275912-71275962	HEEpiC	esophagus:	n/a
36	chr11:71259341-71259391	PrEC	prostate:	n/a
37	chr11:71238382-71238432	NHBE	bronchial:	n/a
38	chr11:71238270-71238320	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:71276557-71276607	SK-N-SH	brain:	n/a
40	chr11:71210210-71210260	ECC-1	luminal epithelium:	n/a
41	chr11:71210295-71210345	HMEC	breast:	n/a
42	chr11:71229988-71230038	Jurkat	blood:	n/a
43	chr11:71238225-71238275	AG09319	gingival:	n/a
44	chr11:71248741-71248791	SK-N-MC	brain:	n/a
45	chr11:71202719-71202769	BE2_C	brain:	n/a
46	chr11:71200489-71200539	ECC-1	luminal epithelium:	n/a
47	chr11:71250073-71250123	HIPEpiC	eye:	n/a
48	chr11:71288514-71288564	HCM	heart:	n/a
49	chr11:71202779-71202829	RPTEC	kidney:	n/a
50	chr11:71237650-71237700	SK-N-SH	brain:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:71214307..71215980-chr11:71218058..71219909,2	K562	blood:
2	chr11:71209374..71211618-chr11:71213015..71214853,2	K562	blood:
3	chr11:71278406..71279386-chr11:71291430..71292089,2	MCF-7	breast:
4	chr11:71212078..71213595-chr11:71215421..71217314,2	K562	blood:
5	chr11:71157948..71159968-chr11:71219705..71221725,2	MCF-7	breast:
6	chr11:71154436..71156970-chr11:71198755..71201662,2	MCF-7	breast:
7	chr11:71282448..71285837-chr11:71286010..71289392,3	MCF-7	breast:
8	chr11:71210029..71213708-chr11:71213873..71217585,6	MCF-7	breast:
9	chr11:71279845..71280406-chr11:71290008..71290749,2	MCF-7	breast:
10	chr11:71209230..71212129-chr11:71251545..71253303,2	MCF-7	breast:
11	chr11:71257442..71259140-chr11:71259571..71262525,2	K562	blood:
12	chr11:71272055..71274887-chr11:71280546..71282110,2	K562	blood:
13	chr11:71192234..71193164-chr11:71211678..71212297,4	MCF-7	breast:
14	chr11:71198148..71200436-chr11:71273726..71275977,2	MCF-7	breast:
15	chr11:71198148..71200436-chr11:71273726..71275977,2	MCF-7	breast:
16	chr11:71158604..71160379-chr11:71280505..71283180,2	MCF-7	breast:
17	chr11:71284028..71285602-chr11:71289697..71292475,2	MCF-7	breast:
18	chr11:71205951..71209347-chr11:71211780..71215363,4	MCF-7	breast:
19	chr11:71214508..71217959-chr11:71220127..71223025,3	MCF-7	breast:
20	chr11:71198072..71200599-chr11:71283906..71285709,2	MCF-7	breast:
21	chr11:71189071..71191550-chr11:71272066..71273804,2	MCF-7	breast:
22	chr11:71202765..71205169-chr11:71209024..71211157,2	K562	blood:
23	chr11:71278628..71280477-chr11:71289049..71291000,2	MCF-7	breast:
24	chr11:71253515..71257343-chr11:71260479..71262893,3	MCF-7	breast:
25	chr11:71279425..71280036-chr11:71290519..71291383,2	MCF-7	breast:
26	chr11:71212078..71213595-chr11:71215421..71217314,2	K562	blood:
27	chr11:71191263..71193677-chr11:71202441..71204415,2	MCF-7	breast:
28	chr11:71282448..71285837-chr11:71286010..71289392,3	MCF-7	breast:
29	chr11:71214959..71216939-chr11:71218643..71221307,2	K562	blood:
30	chr11:71257442..71259140-chr11:71259571..71262525,2	K562	blood:
31	chr11:71188326..71191003-chr11:71198229..71200768,2	K562	blood:
32	chr11:71199654..71202041-chr11:71202100..71204531,2	K562	blood:
33	chr11:71230161..71233081-chr11:71237007..71238796,2	MCF-7	breast:
34	chr11:71198072..71200599-chr11:71283906..71285709,2	MCF-7	breast:
35	chr11:71156994..71165841-chr11:71185066..71202614,31	MCF-7	breast:
36	chr11:71197542..71205760-chr11:71207868..71214040,12	MCF-7	breast:
37	chr11:71221136..71223101-chr11:71257935..71260917,2	MCF-7	breast:
38	chr11:71176264..71179140-chr11:71273245..71275842,2	MCF-7	breast:
39	chr11:71197776..71200724-chr11:71214372..71216917,2	MCF-7	breast:
40	chr11:71214959..71216939-chr11:71218643..71221307,2	K562	blood:
41	chr11:71254168..71255682-chr11:71257713..71259935,2	MCF-7	breast:
42	chr11:71159116..71165503-chr11:71274687..71279227,9	MCF-7	breast:
43	chr11:71209374..71211618-chr11:71213015..71214853,2	K562	blood:
44	chr11:71162728..71165710-chr11:71209612..71212447,2	K562	blood:
45	chr11:71199654..71202041-chr11:71202100..71204531,2	K562	blood:
46	chr11:71198500..71200702-chr11:71204795..71207728,3	MCF-7	breast:
47	chr11:71162651..71164294-chr11:71282060..71284159,2	K562	blood:
48	chr11:71253515..71257343-chr11:71260479..71262893,3	MCF-7	breast:
49	chr11:71205951..71209347-chr11:71211780..71215363,4	MCF-7	breast:
50	chr11:71192889..71195578-chr11:71229380..71232124,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTAP5-7-1	chr11:71214591-71214787	NONHSAT022689
2	lnc-KRTAP5-7-1	chr11:71215112-71215524	NONHSAT022689
3	lnc-KRTAP5-7-1	chr11:71214910-71216920	NONHSAT022690
4	lnc-KRTAP5-10-1	chr11:71279726-71279980	NONHSAT022692
5	lnc-DHCR7-4	chr11:71217107-71217426	NONHSAT022691

No data

Variant related genes	Relation type
KRTAP5-10	TF binding region
KRTAP5-9	TF binding region
ENSG00000248903	TF binding region
ENSG00000254924	TF binding region
NADSYN1	TF binding region
KRTAP5-7	TF binding region
KRTAP5-8	TF binding region
KRTAP5-10	CpG island
KRTAP5-9	CpG island
ENSG00000248903	CpG island
ENSG00000254924	CpG island
NADSYN1	CpG island
KRTAP5-7	CpG island
KRTAP5-8	CpG island
ENSG00000172893	chromatin interactions
ENSG00000254924	chromatin interactions
ENSG00000248903	chromatin interactions
ENSG00000254997	chromatin interactions
ENSG00000172890	chromatin interactions
ENSG00000249387	chromatin interactions
ENSG00000244411	chromatin interactions
ENSG00000254682	chromatin interactions

Extended variants
information (count: 4227 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:4227 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs949178	chr11:71200320-71200321	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561825466	chr11:71200397-71200398	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs7117446	chr11:71200408-71200409	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs529297418	chr11:71200440-71200441	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs147040503	chr11:71200483-71200484	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs5792561	chr11:71200489-71200490	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs35149281	chr11:71200490-71200491	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs11233902	chr11:71200493-71200494	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs559283843	chr11:71200515-71200516	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs138899379	chr11:71200618-71200619	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs551756908	chr11:71200627-71200628	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs79904898	chr11:71200643-71200644	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs1893058	chr11:71200668-71200669	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs549125478	chr11:71200675-71200676	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs567365344	chr11:71200692-71200693	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs535441336	chr11:71200720-71200721	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs35809668	chr11:71200757-71200758	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs57174491	chr11:71200761-71200762	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs553011951	chr11:71200781-71200782	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs571108489	chr11:71200818-71200819	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs544761692	chr11:71200833-71200834	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs538940459	chr11:71200857-71200858	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs549777722	chr11:71200926-71200927	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs116763380	chr11:71200960-71200961	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
25	rs74327815	chr11:71200973-71200974	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
26	rs542410286	chr11:71200976-71200977	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs191544407	chr11:71201008-71201009	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs58732390	chr11:71201009-71201010	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs541081594	chr11:71201018-71201019	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs113681958	chr11:71201044-71201045	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs35816375	chr11:71201060-71201061	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs141670178	chr11:71201062-71201063	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs533138839	chr11:71201100-71201101	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs557559313	chr11:71201115-71201116	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs374035631	chr11:71201116-71201117	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs367626565	chr11:71201178-71201179	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs563804543	chr11:71201194-71201195	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs182986239	chr11:71201195-71201196	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs753352	chr11:71201198-71201199	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs567819172	chr11:71201216-71201217	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs186263513	chr11:71201219-71201220	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs546689307	chr11:71201235-71201236	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs571256643	chr11:71201238-71201239	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs554127296	chr11:71201246-71201247	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs538235872	chr11:71201247-71201248	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs557270359	chr11:71201268-71201269	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs572493364	chr11:71201269-71201270	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs145979319	chr11:71201270-71201271	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs373094087	chr11:71201376-71201377	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs561190401	chr11:71201414-71201415	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1029 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71165000-71210000	Weak transcription	Psoas Muscle	Psoas
2	chr11:71165800-71218400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:71181400-71217800	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr11:71181800-71218000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr11:71182000-71217600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:71182200-71211000	Strong transcription	Liver	Liver
7	chr11:71182200-71216000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:71182200-71216200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:71182200-71216200	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr11:71182200-71217800	Strong transcription	Primary T cells from cord blood	blood
11	chr11:71182400-71213800	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr11:71182400-71217200	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr11:71182400-71217600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:71182400-71217800	Strong transcription	Duodenum Mucosa	Duodenum
15	chr11:71182600-71204000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:71182600-71210200	Strong transcription	Thymus	Thymus
17	chr11:71182600-71213600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:71182800-71216400	Strong transcription	Stomach Smooth Muscle	stomach
19	chr11:71183000-71213400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:71189800-71218400	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr11:71195200-71203000	Weak transcription	Stomach Mucosa	stomach
22	chr11:71195400-71204400	Weak transcription	Hela-S3	cervix
23	chr11:71195400-71206000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr11:71195600-71201200	Weak transcription	Small Intestine	intestine
25	chr11:71195600-71208000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr11:71196200-71209600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr11:71196400-71207600	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr11:71197000-71200800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr11:71197000-71201800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr11:71197000-71202000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr11:71197400-71205200	Weak transcription	Colon Smooth Muscle	Colon
32	chr11:71197600-71200400	Weak transcription	Right Ventricle	heart
33	chr11:71197600-71200800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr11:71197600-71200800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr11:71197600-71200800	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr11:71197600-71202000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr11:71197600-71206400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr11:71197800-71200400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr11:71197800-71200600	Weak transcription	Aorta	Aorta
40	chr11:71197800-71200600	Weak transcription	Brain Angular Gyrus	brain
41	chr11:71197800-71200600	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr11:71197800-71200600	Weak transcription	Fetal Thymus	thymus
43	chr11:71197800-71201200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr11:71197800-71201800	Weak transcription	Left Ventricle	heart
45	chr11:71197800-71202000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr11:71197800-71202400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr11:71197800-71202800	Weak transcription	Primary hematopoietic stem cells	blood
48	chr11:71197800-71205200	Weak transcription	Rectal Smooth Muscle	rectum
49	chr11:71197800-71206000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr11:71197800-71208400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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