Variant report

Variant	nsv545377
Chromosome Location	chr1:9597237-9602962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:9597804-9598357	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:9599103-9599386	HepG2	liver:	n/a	n/a
3	ATF1	chr1:9599196-9599622	K562	blood:	n/a	n/a
4	ATF2	chr1:9599023-9599571	H1-hESC	embryonic stem cell:	n/a	chr1:9599473-9599484
5	ATF2	chr1:9599206-9599630	GM12878	blood:	n/a	chr1:9599473-9599484
6	ATF3	chr1:9599276-9599638	K562	blood:	n/a	chr1:9599473-9599484 chr1:9599472-9599485 chr1:9599496-9599516 chr1:9599472-9599482 chr1:9599485-9599505 chr1:9599474-9599482 chr1:9599472-9599482 chr1:9599475-9599482 chr1:9599474-9599494 chr1:9599463-9599483 chr1:9599473-9599484 chr1:9599475-9599485 chr1:9599471-9599484 chr1:9599471-9599486 chr1:9599473-9599486 chr1:9599475-9599485 chr1:9599472-9599485 chr1:9599475-9599483 chr1:9599508-9599517
7	ATF3	chr1:9599283-9599591	GM12878	blood:	n/a	chr1:9599473-9599484 chr1:9599472-9599485 chr1:9599496-9599516 chr1:9599472-9599482 chr1:9599485-9599505 chr1:9599474-9599482 chr1:9599472-9599482 chr1:9599475-9599482 chr1:9599474-9599494 chr1:9599463-9599483 chr1:9599473-9599484 chr1:9599475-9599485 chr1:9599471-9599484 chr1:9599471-9599486 chr1:9599473-9599486 chr1:9599475-9599485 chr1:9599472-9599485 chr1:9599475-9599483 chr1:9599508-9599517
8	ATF3	chr1:9599387-9599626	GM12878	blood:	n/a	chr1:9599473-9599484 chr1:9599472-9599485 chr1:9599496-9599516 chr1:9599472-9599482 chr1:9599485-9599505 chr1:9599474-9599482 chr1:9599472-9599482 chr1:9599475-9599482 chr1:9599474-9599494 chr1:9599463-9599483 chr1:9599473-9599484 chr1:9599475-9599485 chr1:9599471-9599484 chr1:9599471-9599486 chr1:9599473-9599486 chr1:9599475-9599485 chr1:9599472-9599485 chr1:9599475-9599483 chr1:9599508-9599517
9	ATF3	chr1:9599351-9599611	HepG2	liver:	n/a	chr1:9599473-9599484 chr1:9599472-9599485 chr1:9599496-9599516 chr1:9599472-9599482 chr1:9599485-9599505 chr1:9599474-9599482 chr1:9599472-9599482 chr1:9599475-9599482 chr1:9599474-9599494 chr1:9599463-9599483 chr1:9599473-9599484 chr1:9599475-9599485 chr1:9599471-9599484 chr1:9599471-9599486 chr1:9599473-9599486 chr1:9599475-9599485 chr1:9599472-9599485 chr1:9599475-9599483 chr1:9599508-9599517
10	ATF3	chr1:9599342-9599682	H1-hESC	embryonic stem cell:	n/a	chr1:9599473-9599484 chr1:9599472-9599485 chr1:9599496-9599516 chr1:9599472-9599482 chr1:9599485-9599505 chr1:9599474-9599482 chr1:9599472-9599482 chr1:9599475-9599482 chr1:9599474-9599494 chr1:9599463-9599483 chr1:9599473-9599484 chr1:9599475-9599485 chr1:9599471-9599484 chr1:9599471-9599486 chr1:9599473-9599486 chr1:9599475-9599485 chr1:9599472-9599485 chr1:9599475-9599483 chr1:9599508-9599517
11	BACH1	chr1:9599134-9599634	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr1:9599222-9600293	GM12878	blood:	n/a	chr1:9599494-9599507
13	BHLHE40	chr1:9598963-9600458	K562	blood:	n/a	chr1:9599494-9599507
14	BHLHE40	chr1:9599369-9599564	HepG2	liver:	n/a	chr1:9599494-9599507
15	BHLHE40	chr1:9599352-9599606	A549	lung:	n/a	chr1:9599494-9599507
16	BHLHE40	chr1:9599112-9599719	HepG2	liver:	n/a	chr1:9599494-9599507
17	BHLHE40	chr1:9599271-9599670	HepG2	liver:	n/a	chr1:9599494-9599507
18	BRCA1	chr1:9599088-9599644	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr1:9599058-9599449	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr1:9600075-9600403	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:9599087-9599547	GM12878	blood:	n/a	n/a
22	BRCA1	chr1:9599087-9599615	HepG2	liver:	n/a	n/a
23	CBX3	chr1:9598786-9599532	K562	blood:	n/a	n/a
24	CBX3	chr1:9599973-9600886	K562	blood:	n/a	n/a
25	CCNT2	chr1:9598904-9600430	K562	blood:	n/a	chr1:9600151-9600160 chr1:9600145-9600154
26	CEBPB	chr1:9599202-9599526	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:9599148-9599556	A549	lung:	n/a	n/a
28	CEBPB	chr1:9600211-9600310	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:9597942-9598250	HepG2	liver:	n/a	chr1:9598084-9598096
30	CEBPB	chr1:9600297-9600523	K562	blood:	n/a	n/a
31	CEBPB	chr1:9599214-9599560	MCF-7	breast:	n/a	n/a
32	CEBPB	chr1:9599193-9599517	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr1:9599172-9599569	K562	blood:	n/a	n/a
34	CEBPB	chr1:9599024-9599549	K562	blood:	n/a	n/a
35	CEBPB	chr1:9600172-9600553	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:9599184-9599702	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:9599183-9599658	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:9599189-9599561	A549	lung:	n/a	n/a
39	CEBPB	chr1:9599146-9599533	MCF-7	breast:	n/a	n/a
40	CEBPB	chr1:9599187-9599572	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:9599077-9599573	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:9599252-9599494	A549	lung:	n/a	n/a
43	CEBPB	chr1:9599148-9599497	K562	blood:	n/a	n/a
44	CEBPB	chr1:9599254-9599621	HepG2	liver:	n/a	n/a
45	CEBPD	chr1:9599208-9599656	HepG2	liver:	n/a	n/a
46	CEBPD	chr1:9599368-9599666	HepG2	liver:	n/a	n/a
47	CEBPD	chr1:9598043-9598407	HepG2	liver:	n/a	n/a
48	CEBPD	chr1:9598849-9599624	K562	blood:	n/a	n/a
49	CEBPD	chr1:9597917-9598226	HepG2	liver:	n/a	n/a
50	CHD1	chr1:9600215-9600302	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:9599380-9599430	GM12878	blood:	n/a
2	chr1:9598932-9598982	GM19239	blood:	n/a
3	chr1:9602701-9602751	NB4	blood:	n/a
4	chr1:9599380-9599430	GM12878	blood:	n/a
5	chr1:9598932-9598982	GM19239	blood:	n/a
6	chr1:9602701-9602751	NB4	blood:	n/a
7	chr1:9599067-9599117	Hela-S3	cervix:	n/a
8	chr1:9599391-9599441	NH-A	brain:	n/a
9	chr1:9598983-9599033	BE2_C	brain:	n/a
10	chr1:9600345-9600395	AoSMC	blood vessel:	n/a
11	chr1:9599419-9599469	AG04450	lung:	fetal
12	chr1:9602701-9602751	NHBE	bronchial:	n/a
13	chr1:9599674-9599724	HRE	kidney:	n/a
14	chr1:9600115-9600165	HMEC	breast:	n/a
15	chr1:9599674-9599724	MCF-7	breast:	n/a
16	chr1:9598983-9599033	HRE	kidney:	n/a
17	chr1:9598983-9599033	HCM	heart:	n/a
18	chr1:9599419-9599469	Jurkat	blood:	n/a
19	chr1:9599256-9599306	NT2-D1	testis:	n/a
20	chr1:9600345-9600395	HNPCEpiC	eye:	n/a
21	chr1:9599419-9599469	T-47D	breast:	n/a
22	chr1:9600721-9600771	CMK	blood:	n/a
23	chr1:9599026-9599076	K562	blood:	n/a
24	chr1:9600443-9600493	NHDF-neo	bronchial:	n/a
25	chr1:9602701-9602751	BE2_C	brain:	n/a
26	chr1:9599403-9599453	NB4	blood:	n/a
27	chr1:9599380-9599430	RPTEC	kidney:	n/a
28	chr1:9602701-9602751	PrEC	prostate:	n/a
29	chr1:9598932-9598982	GM12878	blood:	n/a
30	chr1:9600115-9600165	AG09319	gingival:	n/a
31	chr1:9599256-9599306	K562	blood:	n/a
32	chr1:9600115-9600165	SK-N-MC	brain:	n/a
33	chr1:9599391-9599441	IMR90	lung:	fetal
34	chr1:9600345-9600395	NT2-D1	testis:	n/a
35	chr1:9600345-9600395	Hela-S3	cervix:	n/a
36	chr1:9602701-9602751	Hepatocyte	liver:	n/a
37	chr1:9599391-9599441	BE2_C	brain:	n/a
38	chr1:9599674-9599724	K562	blood:	n/a
39	chr1:9599256-9599306	HAEpiC	amniotic membrane:	n/a
40	chr1:9599380-9599430	AG04449	skin:	fetal
41	chr1:9599674-9599724	T-47D	breast:	n/a
42	chr1:9599276-9599326	BJ	skin:	n/a
43	chr1:9599067-9599117	Caco-2	colon:	n/a
44	chr1:9599419-9599469	HIPEpiC	eye:	n/a
45	chr1:9599256-9599306	AG09309	skin:	n/a
46	chr1:9599026-9599076	HMEC	breast:	n/a
47	chr1:9599674-9599724	SK-N-SH	brain:	n/a
48	chr1:9600115-9600165	SAEC	small airway:	n/a
49	chr1:9600443-9600493	HCT-116	colon:	n/a
50	chr1:9599067-9599117	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:9600120..9603287-chr1:9652178..9655376,3	K562	blood:
2	chr1:9599545..9601173-chr1:9607657..9610579,2	MCF-7	breast:
3	chr1:9599309..9599945-chr20:48599375..48600280,2	Hela-S3	cervix:
4	chr1:9599360..9599951-chr2:43453657..43454519,2	NB4	blood:
5	chr1:9597781..9602686-chr1:9646599..9652829,9	K562	blood:
6	chr1:9597398..9600888-chr1:9600968..9602774,3	MCF-7	breast:
7	chr1:9599401..9600258-chr2:55277246..55277773,2	Hela-S3	cervix:
8	chr1:9601186..9603227-chr1:9650193..9652008,2	K562	blood:
9	chr1:9599233..9600127-chr6:111279644..111280229,2	Hela-S3	cervix:
10	chr1:9602754..9605108-chr1:9639045..9641242,2	K562	blood:
11	chr1:9597734..9599433-chr1:9617661..9619736,2	K562	blood:
12	chr1:9586876..9589181-chr1:9596662..9599409,2	K562	blood:
13	chr1:9294638..9296253-chr1:9598479..9600330,2	K562	blood:
14	chr1:9600243..9601816-chr1:9629170..9632084,2	K562	blood:
15	chr1:9350586..9353918-chr1:9597167..9600975,3	MCF-7	breast:
16	chr1:9599430..9599966-chr2:162164733..162165342,2	Hela-S3	cervix:
17	chr1:9596866..9598419-chr1:9883166..9885475,2	K562	blood:
18	chr1:9599090..9600004-chr11:94964653..94965231,2	NB4	blood:
19	chr1:9599460..9600393-chr11:92930413..92931236,2	NB4	blood:
20	chr1:9587010..9589066-chr1:9600375..9602701,2	K562	blood:
21	chr1:9597937..9599836-chr1:9648693..9652829,4	K562	blood:
22	chr1:9599563..9600515-chr15:65588090..65588719,2	Hela-S3	cervix:
23	chr1:9594978..9597511-chr1:9598166..9600611,4	K562	blood:

Variant related genes	Relation type
SLC25A33	TF binding region
SLC25A33	CpG island
ENSG00000171621	chromatin interactions
ENSG00000115310	chromatin interactions
ENSG00000115233	chromatin interactions
ENSG00000124216	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000180773	chromatin interactions
ENSG00000245552	chromatin interactions
ENSG00000155115	chromatin interactions
ENSG00000049239	chromatin interactions
ENSG00000171612	chromatin interactions
ENSG00000171603	chromatin interactions
ENSG00000152518	chromatin interactions
ENSG00000188807	chromatin interactions

Extended variants
information (count: 177 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:177 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554741920	chr1:9597241-9597242	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs376237825	chr1:9597252-9597253	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs188047750	chr1:9597263-9597264	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs192507609	chr1:9597275-9597276	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs184640966	chr1:9597292-9597293	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs188303554	chr1:9597308-9597309	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs192938725	chr1:9597330-9597331	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs562717538	chr1:9597356-9597357	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs533513825	chr1:9597389-9597390	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs551575562	chr1:9597473-9597474	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs184628595	chr1:9597488-9597489	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs527891886	chr1:9597497-9597498	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs549572086	chr1:9597622-9597623	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs567977685	chr1:9597649-9597650	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs377641688	chr1:9597658-9597659	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs371107741	chr1:9597659-9597660	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs375457902	chr1:9597666-9597667	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs538143949	chr1:9597705-9597706	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs146433477	chr1:9597706-9597707	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs549779000	chr1:9597731-9597732	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs537308329	chr1:9597739-9597740	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs571154431	chr1:9597751-9597752	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs140790532	chr1:9597752-9597753	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs72646713	chr1:9597847-9597848	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs77366460	chr1:9597919-9597920	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs12022881	chr1:9597923-9597924	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs554327142	chr1:9597948-9597949	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs372341082	chr1:9598015-9598016	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs57585081	chr1:9598175-9598176	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562942554	chr1:9598208-9598209	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs538749797	chr1:9598266-9598267	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs577968606	chr1:9598269-9598270	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs545340441	chr1:9598365-9598366	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs556994989	chr1:9598397-9598398	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs189462120	chr1:9598399-9598400	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs76491091	chr1:9598552-9598553	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs75303328	chr1:9598564-9598565	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs144722371	chr1:9598611-9598612	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs113561944	chr1:9598679-9598680	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs550214497	chr1:9598696-9598697	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs571860163	chr1:9598814-9598815	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs568952241	chr1:9598830-9598831	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs181041436	chr1:9598877-9598878	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs529082109	chr1:9598914-9598915	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs538075663	chr1:9598943-9598944	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs111714926	chr1:9598974-9598975	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs55655211	chr1:9598991-9598992	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs554882642	chr1:9599027-9599028	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs536491286	chr1:9599078-9599079	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs113589383	chr1:9599119-9599120	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	20406844	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:9555800-9599400	Weak transcription	Right Atrium	heart
2	chr1:9587200-9598200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:9591600-9598200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:9591600-9599000	Weak transcription	Adipose Nuclei	Adipose
5	chr1:9591600-9599400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:9592000-9598000	Weak transcription	Fetal Heart	heart
7	chr1:9593200-9598600	Weak transcription	Brain Anterior Caudate	brain
8	chr1:9593200-9599000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:9593400-9597800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:9593400-9597800	Weak transcription	Liver	Liver
11	chr1:9593400-9598000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:9593400-9598400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:9593400-9598600	Weak transcription	Fetal Lung	lung
14	chr1:9593400-9598800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:9593400-9598800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:9593400-9598800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr1:9593600-9598000	Weak transcription	Brain Substantia Nigra	brain
18	chr1:9593600-9598200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr1:9593600-9598200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr1:9593600-9598400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:9593600-9598800	Weak transcription	Brain Hippocampus Middle	brain
22	chr1:9593600-9599000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:9593600-9599000	Weak transcription	Brain Angular Gyrus	brain
24	chr1:9593600-9599600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:9593800-9599000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr1:9594400-9599400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr1:9594600-9599000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:9596200-9599400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr1:9596400-9597800	Enhancers	HepG2	liver
30	chr1:9596800-9598000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr1:9597000-9597800	Weak transcription	Fetal Intestine Small	intestine
32	chr1:9597200-9597800	Enhancers	Fetal Intestine Large	intestine
33	chr1:9597200-9599200	Enhancers	Stomach Mucosa	stomach
34	chr1:9597600-9597800	Enhancers	Duodenum Mucosa	Duodenum
35	chr1:9597800-9598000	Flanking Active TSS	Liver	Liver
36	chr1:9597800-9598000	Enhancers	Fetal Intestine Small	intestine
37	chr1:9597800-9598000	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr1:9597800-9598200	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr1:9597800-9598200	Enhancers	Small Intestine	intestine
40	chr1:9597800-9598400	Flanking Active TSS	Duodenum Mucosa	Duodenum
41	chr1:9597800-9598400	Enhancers	K562	blood
42	chr1:9597800-9598600	Flanking Active TSS	Fetal Intestine Large	intestine
43	chr1:9597800-9598800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:9597800-9598800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:9597800-9599200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr1:9597800-9599200	Flanking Active TSS	HepG2	liver
47	chr1:9597800-9599400	Enhancers	HMEC	breast
48	chr1:9597800-9599600	Enhancers	GM12878-XiMat	blood
49	chr1:9598000-9598200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:9598000-9598200	Enhancers	Primary hematopoietic stem cells	blood

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