Variant report

Variant	nsv1022782
Chromosome Location	chr7:150970748-150992935
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:199)
CpG islands
(count:610)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:199 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150974271-150974336	K562	blood:	n/a	n/a
2	ATF1	chr7:150987484-150987684	K562	blood:	n/a	n/a
3	ATF3	chr7:150985735-150985968	K562	blood:	n/a	n/a
4	BCL3	chr7:150977738-150977991	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:150974243-150974589	K562	blood:	n/a	n/a
6	CBX3	chr7:150974161-150974766	K562	blood:	n/a	n/a
7	CCNT2	chr7:150974070-150974376	K562	blood:	n/a	n/a
8	CEBPB	chr7:150974232-150974476	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr7:150987028-150987221	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:150975535-150975867	K562	blood:	n/a	chr7:150975689-150975700
11	CEBPB	chr7:150975572-150975774	HepG2	liver:	n/a	chr7:150975689-150975700
12	CEBPB	chr7:150987028-150987288	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr7:150987048-150987362	K562	blood:	n/a	n/a
14	CEBPB	chr7:150991056-150991072	K562	blood:	n/a	n/a
15	CEBPB	chr7:150989996-150990294	K562	blood:	n/a	n/a
16	CEBPB	chr7:150980369-150980564	HepG2	liver:	n/a	chr7:150980398-150980409
17	CEBPB	chr7:150975598-150975868	A549	lung:	n/a	chr7:150975689-150975700
18	CEBPB	chr7:150987097-150987243	K562	blood:	n/a	n/a
19	CEBPB	chr7:150987102-150987730	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:150975612-150975851	IMR90	lung:	n/a	chr7:150975689-150975700
21	CEBPB	chr7:150973357-150973617	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:150988427-150988623	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:150987051-150987352	K562	blood:	n/a	n/a
24	CHD2	chr7:150974277-150974287	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr7:150973480-150973492	Hela-S3	cervix:	n/a	n/a
26	CREB1	chr7:150974056-150974510	A549	lung:	n/a	n/a
27	CTCF	chr7:150974906-150974946	GM13976	blood:	n/a	n/a
28	CTCF	chr7:150989360-150989510	A549	lung:	n/a	n/a
29	CTCF	chr7:150989518-150989539	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:150989400-150989550	HepG2	liver:	n/a	n/a
31	CTCF	chr7:150989422-150989574	HepG2	liver:	n/a	n/a
32	CTCF	chr7:150989503-150989522	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:150989360-150989510	Caco-2	colon:	n/a	n/a
34	CTCF	chr7:150975095-150975186	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:150989448-150989574	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:150989440-150989590	HEK293	kidney:	n/a	n/a
37	CTCF	chr7:150989360-150989510	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr7:150989360-150989510	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr7:150984320-150984470	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr7:150989320-150989470	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:150989400-150989550	HA-sp	spinal cord:	n/a	n/a
42	CUX1	chr7:150974485-150974518	K562	blood:	n/a	n/a
43	E2F4	chr7:150974311-150974444	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F6	chr7:150974114-150974621	K562	blood:	n/a	chr7:150974230-150974239 chr7:150974227-150974237
45	EGR1	chr7:150974048-150974624	K562	blood:	n/a	chr7:150974251-150974264 chr7:150974230-150974239 chr7:150974252-150974266
46	EGR1	chr7:150974142-150974350	GM12878	blood:	n/a	chr7:150974251-150974264 chr7:150974230-150974239 chr7:150974252-150974266
47	EGR1	chr7:150974054-150974481	ECC-1	luminal epithelium:	n/a	chr7:150974251-150974264 chr7:150974230-150974239 chr7:150974252-150974266
48	EGR1	chr7:150973967-150974710	HCT-116	colon:	n/a	chr7:150974639-150974654 chr7:150974251-150974264 chr7:150974640-150974653 chr7:150974230-150974239 chr7:150974252-150974266
49	EGR1	chr7:150974015-150974519	H1-hESC	embryonic stem cell:	n/a	chr7:150974251-150974264 chr7:150974230-150974239 chr7:150974252-150974266
50	EGR1	chr7:150974033-150974790	K562	blood:	n/a	chr7:150974639-150974654 chr7:150974251-150974264 chr7:150974640-150974653 chr7:150974230-150974239 chr7:150974252-150974266

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150972305-150972355	HCPEpiC	choroid plexus:	n/a
2	chr7:150974273-150974323	NHBE	bronchial:	n/a
3	chr7:150974453-150974503	HEK293	kidney:	embryo
4	chr7:150974464-150974514	SK-N-SH_RA	brain:	n/a
5	chr7:150974391-150974441	AG04449	skin:	fetal
6	chr7:150974464-150974514	HIPEpiC	eye:	n/a
7	chr7:150974554-150974604	HMEC	breast:	n/a
8	chr7:150974464-150974514	GM12878	blood:	n/a
9	chr7:150974464-150974514	LNCaP	prostate:	n/a
10	chr7:150974464-150974514	HCF	heart:	n/a
11	chr7:150972574-150972624	RPTEC	kidney:	n/a
12	chr7:150974464-150974514	HNPCEpiC	eye:	n/a
13	chr7:150974391-150974441	HL-60	blood:	n/a
14	chr7:150977475-150977525	ovcar-3	ovarian:	n/a
15	chr7:150974554-150974604	AoSMC	blood vessel:	n/a
16	chr7:150977475-150977525	HL-60	blood:	n/a
17	chr7:150972305-150972355	RPTEC	kidney:	n/a
18	chr7:150974554-150974604	LNCaP	prostate:	n/a
19	chr7:150972305-150972355	HCM	heart:	n/a
20	chr7:150974273-150974323	AG04450	lung:	fetal
21	chr7:150974554-150974604	HCPEpiC	choroid plexus:	n/a
22	chr7:150974371-150974421	GM06990	blood:	n/a
23	chr7:150974371-150974421	HCT-116	colon:	n/a
24	chr7:150972574-150972624	HEK293	kidney:	embryo
25	chr7:150972305-150972355	NHBE	bronchial:	n/a
26	chr7:150972574-150972624	PANC-1	pancreas:	n/a
27	chr7:150974273-150974323	NH-A	brain:	n/a
28	chr7:150974273-150974323	HCM	heart:	n/a
29	chr7:150974391-150974441	SKMC	muscle:	n/a
30	chr7:150972574-150972624	HRCEpiC	kidney:	n/a
31	chr7:150974371-150974421	HCPEpiC	choroid plexus:	n/a
32	chr7:150974453-150974503	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:150972305-150972355	NT2-D1	testis:	n/a
34	chr7:150977475-150977525	A549	lung:	n/a
35	chr7:150972574-150972624	HRPEpiC	eye:	n/a
36	chr7:150974464-150974514	GM06990	blood:	n/a
37	chr7:150974453-150974503	AG04449	skin:	fetal
38	chr7:150977475-150977525	HCPEpiC	choroid plexus:	n/a
39	chr7:150974273-150974323	Caco-2	colon:	n/a
40	chr7:150974554-150974604	NHBE	bronchial:	n/a
41	chr7:150972305-150972355	MCF10A-Er-Src	breast:	n/a
42	chr7:150974374-150974424	K562	blood:	n/a
43	chr7:150974374-150974424	ProgFib	skin:	n/a
44	chr7:150972574-150972624	GM12878	blood:	n/a
45	chr7:150974273-150974323	MCF10A-Er-Src	breast:	n/a
46	chr7:150972574-150972624	MCF-7	breast:	n/a
47	chr7:150972574-150972624	ProgFib	skin:	n/a
48	chr7:150972574-150972624	HCT-116	colon:	n/a
49	chr7:150972574-150972624	HAEpiC	amniotic membrane:	n/a
50	chr7:150974464-150974514	HRPEpiC	eye:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150984426..150986306-chr7:150996451..150998934,2	MCF-7	breast:
2	chr7:150977323..150979463-chr7:150981441..150983335,3	K562	blood:
3	chr7:150972599..150974856-chr7:151038814..151040776,2	MCF-7	breast:
4	chr7:150923971..150925972-chr7:150969624..150971885,2	K562	blood:
5	chr7:150979875..150983495-chr7:150985086..150987532,3	K562	blood:
6	chr7:150969410..150970989-chr7:150972695..150974357,2	K562	blood:
7	chr7:150944159..150946342-chr7:150972887..150975150,2	MCF-7	breast:
8	chr7:150928977..150930907-chr7:150983149..150985560,2	MCF-7	breast:
9	chr7:150968703..150971199-chr7:150976424..150979575,3	MCF-7	breast:
10	chr7:150809552..150813512-chr7:150971172..150974114,3	MCF-7	breast:
11	chr7:150922541..150925891-chr7:150969834..150974111,4	K562	blood:
12	chr7:150983865..150985433-chr7:150985539..150988444,2	K562	blood:
13	chr7:150965804..150968803-chr7:150979702..150982006,2	K562	blood:
14	chr7:150922344..150925065-chr7:150978218..150980365,2	K562	blood:
15	chr7:150987600..150989961-chr7:150999462..151001040,2	MCF-7	breast:
16	chr7:150941689..150943266-chr7:150971664..150974365,2	K562	blood:
17	chr7:150939223..150941619-chr7:150989727..150991845,2	MCF-7	breast:
18	chr7:150974492..150976036-chr7:150978226..150980422,2	K562	blood:
19	chr7:150979875..150983495-chr7:150985086..150987532,3	K562	blood:
20	chr7:150983865..150985433-chr7:150985539..150988444,2	K562	blood:
21	chr7:150972104..150974306-chr7:150978035..150979802,2	K562	blood:
22	chr7:150943021..150944540-chr7:150987056..150989396,2	K562	blood:
23	chr7:150968703..150971199-chr7:150976424..150979575,3	MCF-7	breast:
24	chr7:150977323..150979463-chr7:150981441..150983335,3	K562	blood:
25	chr7:150971574..150974411-chr7:151038667..151040359,3	K562	blood:
26	chr7:150942643..150944372-chr7:150968463..150970799,2	K562	blood:
27	chr7:150971574..150973333-chr7:151038730..151040359,2	K562	blood:
28	chr7:150968652..150970975-chr7:150971256..150974787,4	MCF-7	breast:
29	chr7:150963840..150966297-chr7:150967879..150970876,2	MCF-7	breast:
30	chr7:150974670..150977274-chr7:150979950..150982470,2	K562	blood:
31	chr7:150945192..150947145-chr7:150976993..150978878,2	K562	blood:

No data

Variant related genes	Relation type
SMARCD3	TF binding region
SMARCD3	CpG island
ENSG00000033050	chromatin interactions
ENSG00000013374	chromatin interactions
ENSG00000243018	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000033100	chromatin interactions
ENSG00000082014	chromatin interactions

Extended variants
information (count: 876 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531162320	chr7:150970751-150970752	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544001371	chr7:150970768-150970769	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs547798729	chr7:150970773-150970774	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567800992	chr7:150970816-150970817	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs533679816	chr7:150970829-150970830	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs553529540	chr7:150970919-150970920	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs182082084	chr7:150970920-150970921	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369761940	chr7:150970925-150970926	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs539232368	chr7:150970926-150970927	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185281032	chr7:150970995-150970996	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576031963	chr7:150971009-150971010	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141532479	chr7:150971038-150971039	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs372032928	chr7:150971059-150971060	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375194472	chr7:150971064-150971065	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150865804	chr7:150971112-150971113	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574963286	chr7:150971113-150971114	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs540415705	chr7:150971141-150971142	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560283911	chr7:150971190-150971191	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs576922885	chr7:150971200-150971201	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535104953	chr7:150971245-150971246	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs139415985	chr7:150971263-150971264	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144139578	chr7:150971264-150971265	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs531534960	chr7:150971326-150971327	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs112312354	chr7:150971341-150971342	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs547762871	chr7:150971360-150971361	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs561394207	chr7:150971394-150971395	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs527372960	chr7:150971401-150971402	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs3789818	chr7:150971430-150971431	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs570533443	chr7:150971441-150971442	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs538832419	chr7:150971476-150971477	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs552817555	chr7:150971485-150971486	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs36009984	chr7:150971513-150971514	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs569552927	chr7:150971543-150971544	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs559818644	chr7:150971612-150971613	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs373981284	chr7:150971622-150971623	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs554997544	chr7:150971632-150971633	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs189691273	chr7:150971663-150971664	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs147325063	chr7:150971668-150971669	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs534206928	chr7:150971673-150971674	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs553929927	chr7:150971682-150971683	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs530108054	chr7:150971684-150971685	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs577288986	chr7:150971727-150971728	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs545665466	chr7:150971747-150971748	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs549344405	chr7:150971781-150971782	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs567554901	chr7:150971782-150971783	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs180899790	chr7:150971791-150971792	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs575929312	chr7:150971792-150971793	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs377309408	chr7:150971818-150971819	Weak transcription Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs541763377	chr7:150971887-150971888	Weak transcription Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs561659754	chr7:150971956-150971957	Weak transcription Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150950400-150973400	Weak transcription	Brain Substantia Nigra	brain
2	chr7:150951000-150970800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr7:150959600-150972800	Weak transcription	Ovary	ovary
4	chr7:150960200-150973200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:150964000-150972000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:150967400-150973000	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr7:150967800-150972800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr7:150968000-150971000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:150968000-150972600	Weak transcription	Brain Hippocampus Middle	brain
10	chr7:150968000-150974000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr7:150968200-150971800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr7:150968200-150973800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr7:150968400-150971400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:150968400-150972000	Weak transcription	Brain Germinal Matrix	brain
15	chr7:150968400-150973200	Weak transcription	Brain Angular Gyrus	brain
16	chr7:150968600-150970800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr7:150969000-150972800	Weak transcription	Colonic Mucosa	Colon
18	chr7:150969000-150973000	Enhancers	Fetal Brain Male	brain
19	chr7:150969000-150973400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr7:150969200-150971400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
21	chr7:150969200-150973200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:150969400-150970800	Enhancers	Fetal Heart	heart
23	chr7:150969400-150972200	Enhancers	Fetal Brain Female	brain
24	chr7:150969400-150972200	Weak transcription	Fetal Intestine Small	intestine
25	chr7:150969600-150972600	Weak transcription	Liver	Liver
26	chr7:150969600-150972800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr7:150969600-150972800	Weak transcription	Colon Smooth Muscle	Colon
28	chr7:150969600-150973000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr7:150969600-150973000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr7:150969600-150973200	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr7:150969600-150973200	Weak transcription	Hela-S3	cervix
32	chr7:150969800-150971200	Weak transcription	Stomach Smooth Muscle	stomach
33	chr7:150969800-150971600	Enhancers	Right Atrium	heart
34	chr7:150969800-150972000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:150969800-150972600	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr7:150969800-150972800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr7:150969800-150972800	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr7:150969800-150972800	Weak transcription	Esophagus	oesophagus
39	chr7:150969800-150973000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr7:150970000-150970800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:150970000-150970800	Weak transcription	Brain Cingulate Gyrus	brain
42	chr7:150970000-150971000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr7:150970000-150971200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:150970000-150971200	Weak transcription	Brain Anterior Caudate	brain
45	chr7:150970000-150971800	Weak transcription	Fetal Muscle Leg	muscle
46	chr7:150970000-150972400	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr7:150970000-150972600	Strong transcription	Fetal Stomach	stomach
48	chr7:150970000-150972800	Weak transcription	Fetal Lung	lung
49	chr7:150970000-150973000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr7:150970000-150973200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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