Variant report

Variant	nsv609036
Chromosome Location	chr7:150951819-150991795
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:734)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

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	ATF1	chr7:150970120-150970355	K562	blood:	n/a	n/a
4	ATF3	chr7:150985735-150985968	K562	blood:	n/a	n/a
5	BCL3	chr7:150977738-150977991	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:150974243-150974589	K562	blood:	n/a	n/a
7	BHLHE40	chr7:150969111-150969774	K562	blood:	n/a	n/a
8	BHLHE40	chr7:150958598-150958681	K562	blood:	n/a	n/a
9	BHLHE40	chr7:150969147-150969401	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:150969069-150969243	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr7:150974161-150974766	K562	blood:	n/a	n/a
12	CBX3	chr7:150968735-150969352	K562	blood:	n/a	n/a
13	CCNT2	chr7:150957046-150957248	K562	blood:	n/a	n/a
14	CCNT2	chr7:150974070-150974376	K562	blood:	n/a	n/a
15	CCNT2	chr7:150970170-150970297	K562	blood:	n/a	n/a
16	CEBPB	chr7:150989996-150990294	K562	blood:	n/a	n/a
17	CEBPB	chr7:150987048-150987362	K562	blood:	n/a	n/a
18	CEBPB	chr7:150969007-150969402	A549	lung:	n/a	chr7:150969208-150969219
19	CEBPB	chr7:150991056-150991072	K562	blood:	n/a	n/a
20	CEBPB	chr7:150988427-150988623	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:150974232-150974476	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:150987097-150987243	K562	blood:	n/a	n/a
23	CEBPB	chr7:150975535-150975867	K562	blood:	n/a	chr7:150975689-150975700
24	CEBPB	chr7:150968932-150969421	Hela-S3	cervix:	n/a	chr7:150969208-150969219
25	CEBPB	chr7:150980369-150980564	HepG2	liver:	n/a	chr7:150980398-150980409
26	CEBPB	chr7:150970197-150970279	K562	blood:	n/a	n/a
27	CEBPB	chr7:150968873-150969494	K562	blood:	n/a	chr7:150969208-150969219
28	CEBPB	chr7:150969025-150969356	H1-hESC	embryonic stem cell:	n/a	chr7:150969208-150969219
29	CEBPB	chr7:150973357-150973617	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:150969008-150969527	MCF-7	breast:	n/a	chr7:150969208-150969219
31	CEBPB	chr7:150987051-150987352	K562	blood:	n/a	n/a
32	CEBPB	chr7:150987028-150987221	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:150969013-150969432	ECC-1	luminal epithelium:	n/a	chr7:150969208-150969219
34	CEBPB	chr7:150987028-150987288	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:150969032-150969418	HepG2	liver:	n/a	chr7:150969208-150969219
36	CEBPB	chr7:150975612-150975851	IMR90	lung:	n/a	chr7:150975689-150975700
37	CEBPB	chr7:150968918-150969449	A549	lung:	n/a	chr7:150969208-150969219
38	CEBPB	chr7:150968998-150969418	ECC-1	luminal epithelium:	n/a	chr7:150969208-150969219
39	CEBPB	chr7:150969005-150969410	K562	blood:	n/a	chr7:150969208-150969219
40	CEBPB	chr7:150968990-150969413	HepG2	liver:	n/a	chr7:150969208-150969219
41	CEBPB	chr7:150975598-150975868	A549	lung:	n/a	chr7:150975689-150975700
42	CEBPB	chr7:150975572-150975774	HepG2	liver:	n/a	chr7:150975689-150975700
43	CEBPB	chr7:150987102-150987730	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:150968916-150969470	MCF-7	breast:	n/a	chr7:150969208-150969219
45	CEBPB	chr7:150969000-150969410	IMR90	lung:	n/a	chr7:150969208-150969219
46	CEBPB	chr7:150969002-150969394	K562	blood:	n/a	chr7:150969208-150969219
47	CEBPD	chr7:150956927-150957380	K562	blood:	n/a	n/a
48	CEBPD	chr7:150956857-150957355	K562	blood:	n/a	n/a
49	CEBPD	chr7:150969987-150970514	K562	blood:	n/a	n/a
50	CEBPD	chr7:150969991-150970455	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150974554-150974604	RPTEC	kidney:	n/a
2	chr7:150972574-150972624	HCM	heart:	n/a
3	chr7:150974554-150974604	RPTEC	kidney:	n/a
4	chr7:150972574-150972624	HCM	heart:	n/a
5	chr7:150969275-150969325	HL-60	blood:	n/a
6	chr7:150974464-150974514	GM06990	blood:	n/a
7	chr7:150974554-150974604	AG04450	lung:	fetal
8	chr7:150974391-150974441	MCF10A-Er-Src	breast:	n/a
9	chr7:150977475-150977525	HIPEpiC	eye:	n/a
10	chr7:150972305-150972355	HEK293	kidney:	embryo
11	chr7:150974464-150974514	HCF	heart:	n/a
12	chr7:150969275-150969325	AG09319	gingival:	n/a
13	chr7:150974554-150974604	SKMC	muscle:	n/a
14	chr7:150974453-150974503	H1-hESC	embryonic stem cell:	embryo
15	chr7:150974273-150974323	HCM	heart:	n/a
16	chr7:150974453-150974503	SKMC	muscle:	n/a
17	chr7:150974453-150974503	ProgFib	skin:	n/a
18	chr7:150970209-150970259	AG09309	skin:	n/a
19	chr7:150972305-150972355	AoSMC	blood vessel:	n/a
20	chr7:150974391-150974441	GM12878	blood:	n/a
21	chr7:150974453-150974503	NHBE	bronchial:	n/a
22	chr7:150972574-150972624	SAEC	small airway:	n/a
23	chr7:150974391-150974441	SK-N-MC	brain:	n/a
24	chr7:150974464-150974514	AG09319	gingival:	n/a
25	chr7:150974554-150974604	NHDF-neo	bronchial:	n/a
26	chr7:150977475-150977525	BE2_C	brain:	n/a
27	chr7:150970209-150970259	NT2-D1	testis:	n/a
28	chr7:150974273-150974323	RPTEC	kidney:	n/a
29	chr7:150974453-150974503	Hepatocyte	liver:	n/a
30	chr7:150974273-150974323	HAEpiC	amniotic membrane:	n/a
31	chr7:150972305-150972355	HAEpiC	amniotic membrane:	n/a
32	chr7:150974453-150974503	Hela-S3	cervix:	n/a
33	chr7:150972305-150972355	HUVEC	blood vessel:	n/a
34	chr7:150974453-150974503	AG09319	gingival:	n/a
35	chr7:150970209-150970259	ProgFib	skin:	n/a
36	chr7:150974273-150974323	AoSMC	blood vessel:	n/a
37	chr7:150972574-150972624	AG09319	gingival:	n/a
38	chr7:150969275-150969325	LNCaP	prostate:	n/a
39	chr7:150974464-150974514	AG04449	skin:	fetal
40	chr7:150974391-150974441	HCM	heart:	n/a
41	chr7:150974371-150974421	GM06990	blood:	n/a
42	chr7:150972574-150972624	HNPCEpiC	eye:	n/a
43	chr7:150974391-150974441	NH-A	brain:	n/a
44	chr7:150972305-150972355	HCF	heart:	n/a
45	chr7:150972574-150972624	GM12891	blood:	n/a
46	chr7:150974371-150974421	ECC-1	luminal epithelium:	n/a
47	chr7:150974374-150974424	ovcar-3	ovarian:	n/a
48	chr7:150974554-150974604	AG10803	skin:	n/a
49	chr7:150970209-150970259	AG10803	skin:	n/a
50	chr7:150972305-150972355	ProgFib	skin:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:150957518..150961137-chr7:150961373..150964885,3	MCF-7	breast:
2	chr7:150955167..150957625-chr7:150960069..150962944,2	K562	blood:
3	chr7:150977323..150979463-chr7:150981441..150983335,3	K562	blood:
4	chr7:150972599..150974856-chr7:151038814..151040776,2	MCF-7	breast:
5	chr7:150942010..150944289-chr7:150955333..150957192,2	K562	blood:
6	chr7:150944159..150946342-chr7:150972887..150975150,2	MCF-7	breast:
7	chr7:150922261..150926651-chr7:150957590..150961100,5	K562	blood:
8	chr7:150945192..150947145-chr7:150976993..150978878,2	K562	blood:
9	chr7:150922344..150925065-chr7:150978218..150980365,2	K562	blood:
10	chr7:150942643..150944372-chr7:150968463..150970799,2	K562	blood:
11	chr7:150977323..150979463-chr7:150981441..150983335,3	K562	blood:
12	chr7:150959444..150963668-chr7:150965575..150968005,4	K562	blood:
13	chr7:150928977..150930907-chr7:150983149..150985560,2	MCF-7	breast:
14	chr7:150974670..150977274-chr7:150979950..150982470,2	K562	blood:
15	chr7:150979875..150983495-chr7:150985086..150987532,3	K562	blood:
16	chr7:150943021..150944540-chr7:150987056..150989396,2	K562	blood:
17	chr7:150987600..150989961-chr7:150999462..151001040,2	MCF-7	breast:
18	chr7:150960428..150964557-chr7:150970073..150973761,4	K562	blood:
19	chr7:150962569..150964522-chr7:150964727..150967253,2	MCF-7	breast:
20	chr7:150965804..150968803-chr7:150979702..150982006,2	K562	blood:
21	chr7:150984426..150986306-chr7:150996451..150998934,2	MCF-7	breast:
22	chr7:150963840..150966297-chr7:150967879..150970876,2	MCF-7	breast:
23	chr7:150968703..150971199-chr7:150976424..150979575,3	MCF-7	breast:
24	chr7:150954107..150956387-chr7:150957972..150959934,2	MCF-7	breast:
25	chr7:150949835..150952279-chr7:150953865..150957966,4	MCF-7	breast:
26	chr7:150956133..150957979-chr7:150960470..150962404,2	MCF-7	breast:
27	chr7:150968652..150970975-chr7:150971256..150974787,4	MCF-7	breast:
28	chr7:150962569..150964522-chr7:150964727..150967253,2	MCF-7	breast:
29	chr7:150940078..150941889-chr7:150957924..150960150,2	MCF-7	breast:
30	chr7:150971574..150973333-chr7:151038730..151040359,2	K562	blood:
31	chr7:150964746..150967806-chr7:150970946..150974318,3	K562	blood:
32	chr7:150963840..150966297-chr7:150967879..150970876,2	MCF-7	breast:
33	chr7:150954107..150956387-chr7:150957972..150959934,2	MCF-7	breast:
34	chr7:150938571..150942838-chr7:150950941..150954111,4	MCF-7	breast:
35	chr7:150952243..150954405-chr7:150956858..150959573,2	K562	blood:
36	chr7:150954098..150959160-chr7:150959832..150962944,4	K562	blood:
37	chr7:150957518..150961137-chr7:150961373..150964885,3	MCF-7	breast:
38	chr7:150928662..150932139-chr7:150946772..150952684,6	MCF-7	breast:
39	chr7:150923971..150925972-chr7:150969624..150971885,2	K562	blood:
40	chr7:150957463..150959908-chr7:150971371..150973824,2	K562	blood:
41	chr7:150979875..150983495-chr7:150985086..150987532,3	K562	blood:
42	chr7:150983865..150985433-chr7:150985539..150988444,2	K562	blood:
43	chr7:150883580..150886456-chr7:150958216..150959775,2	K562	blood:
44	chr7:150974492..150976036-chr7:150978226..150980422,2	K562	blood:
45	chr7:150952243..150954405-chr7:150956858..150959573,2	K562	blood:
46	chr7:150960408..150962210-chr7:150963702..150967987,4	K562	blood:
47	chr7:150969410..150970989-chr7:150972695..150974357,2	K562	blood:
48	chr7:150953242..150955142-chr7:150956991..150958505,2	K562	blood:
49	chr7:150954098..150959160-chr7:150959832..150962944,4	K562	blood:
50	chr7:150964684..150966392-chr7:150966406..150968425,2	MCF-7	breast:

No data

Variant related genes	Relation type
SMARCD3	TF binding region
SMARCD3	CpG island
ENSG00000033100	chromatin interactions
ENSG00000243018	chromatin interactions
ENSG00000013374	chromatin interactions
ENSG00000033050	chromatin interactions
ENSG00000146926	chromatin interactions
ENSG00000082014	chromatin interactions
ENSG00000133612	chromatin interactions

Extended variants
information (count: 1601 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1601 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3789823	chr7:150951819-150951820	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76891721	chr7:150951855-150951856	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs543489336	chr7:150951886-150951887	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs183565857	chr7:150951911-150951912	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs575542674	chr7:150951942-150951943	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538112821	chr7:150951963-150951964	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs116153447	chr7:150951967-150951968	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574688442	chr7:150952030-150952031	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs373457953	chr7:150952072-150952073	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539800379	chr7:150952089-150952090	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145643723	chr7:150952091-150952092	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576831548	chr7:150952128-150952129	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541327861	chr7:150952145-150952146	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs565115989	chr7:150952149-150952150	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs138258974	chr7:150952167-150952168	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563475054	chr7:150952171-150952172	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs561382414	chr7:150952228-150952229	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs115020116	chr7:150952262-150952263	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs186827832	chr7:150952268-150952269	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs566872236	chr7:150952311-150952312	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191648831	chr7:150952324-150952325	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs552729867	chr7:150952383-150952384	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569067752	chr7:150952409-150952410	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs111855976	chr7:150952437-150952438	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs538000405	chr7:150952442-150952443	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs142762787	chr7:150952448-150952449	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs376581151	chr7:150952461-150952462	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568238600	chr7:150952464-150952465	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534112282	chr7:150952479-150952480	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs553473964	chr7:150952487-150952488	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs59828731	chr7:150952545-150952546	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs150649711	chr7:150952549-150952550	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138768560	chr7:150952596-150952597	Weak transcription Genic enhancers Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs575741235	chr7:150952612-150952613	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs183843494	chr7:150952724-150952725	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs561551343	chr7:150952725-150952726	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs61591132	chr7:150952770-150952771	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs540953880	chr7:150952791-150952792	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs2429248	chr7:150952830-150952831	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs189575573	chr7:150952876-150952877	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs149515796	chr7:150952891-150952892	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181675338	chr7:150952946-150952947	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs71533527	chr7:150952970-150952971	Weak transcription Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs80229789	chr7:150952984-150952985	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs79038689	chr7:150952985-150952986	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12668799	chr7:150952990-150952991	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs548048983	chr7:150953016-150953017	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530975128	chr7:150953028-150953029	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185221861	chr7:150953029-150953030	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554084216	chr7:150953033-150953034	Weak transcription Enhancers	Chromatin interactive region	1 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:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150950000-150952000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:150950000-150952800	Enhancers	Right Ventricle	heart
3	chr7:150950200-150952800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr7:150950200-150953600	Weak transcription	Brain Anterior Caudate	brain
5	chr7:150950200-150953600	Weak transcription	Brain Hippocampus Middle	brain
6	chr7:150950400-150952000	Weak transcription	Ovary	ovary
7	chr7:150950400-150952200	Enhancers	Fetal Brain Male	brain
8	chr7:150950400-150973400	Weak transcription	Brain Substantia Nigra	brain
9	chr7:150950600-150952400	Enhancers	Fetal Muscle Leg	muscle
10	chr7:150950600-150952600	Weak transcription	Colon Smooth Muscle	Colon
11	chr7:150950600-150953600	Weak transcription	Gastric	stomach
12	chr7:150950600-150953800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr7:150950600-150955400	Weak transcription	Lung	lung
14	chr7:150950600-150955600	Weak transcription	Esophagus	oesophagus
15	chr7:150950600-150957200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr7:150950600-150957800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr7:150950600-150958400	Weak transcription	Right Atrium	heart
18	chr7:150950600-150961400	Weak transcription	Spleen	Spleen
19	chr7:150950600-150965200	Weak transcription	Brain Angular Gyrus	brain
20	chr7:150950600-150967600	Weak transcription	Pancreas	Pancrea
21	chr7:150950800-150953600	Weak transcription	Fetal Heart	heart
22	chr7:150951000-150965400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr7:150951000-150969800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:150951000-150970800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr7:150951200-150952000	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr7:150951200-150952600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:150951200-150952800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr7:150951200-150953600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr7:150951600-150952600	Enhancers	Stomach Smooth Muscle	stomach
30	chr7:150951600-150968000	Weak transcription	Brain Germinal Matrix	brain
31	chr7:150951800-150952600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:150951800-150953600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr7:150951800-150967600	Weak transcription	Fetal Brain Female	brain
34	chr7:150952000-150952400	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:150952000-150953000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr7:150952000-150953800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:150952000-150954400	Enhancers	Ovary	ovary
38	chr7:150952400-150952600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:150952400-150952600	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr7:150952400-150952800	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr7:150952400-150953000	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr7:150952600-150952800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:150952600-150952800	Enhancers	Colon Smooth Muscle	Colon
44	chr7:150952600-150953600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:150952800-150958800	Weak transcription	Right Ventricle	heart
46	chr7:150953600-150953800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr7:150953600-150953800	Bivalent Enhancer	HSMM	muscle
48	chr7:150953600-150953800	Enhancers	HSMMtube	muscle
49	chr7:150953600-150954000	Enhancers	Brain Anterior Caudate	brain
50	chr7:150953600-150954000	Enhancers	Brain Inferior Temporal Lobe	brain

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