Variant report

Variant	esv2476310
Chromosome Location	chr1:9593578-9600139
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	chr1:9596417-9596453	K562	blood:	n/a	n/a
2	ARID3A	chr1:9599103-9599386	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:9597804-9598357	HepG2	liver:	n/a	n/a
4	ATF1	chr1:9599196-9599622	K562	blood:	n/a	n/a
5	ATF2	chr1:9599206-9599630	GM12878	blood:	n/a	chr1:9599473-9599484
6	ATF2	chr1:9599023-9599571	H1-hESC	embryonic stem cell:	n/a	chr1:9599473-9599484
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	chr1:9599276-9599638	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
9	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
10	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
11	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
12	BACH1	chr1:9599134-9599634	H1-hESC	embryonic stem cell:	n/a	n/a
13	BHLHE40	chr1:9599352-9599606	A549	lung:	n/a	chr1:9599494-9599507
14	BHLHE40	chr1:9599369-9599564	HepG2	liver:	n/a	chr1:9599494-9599507
15	BHLHE40	chr1:9599222-9600293	GM12878	blood:	n/a	chr1:9599494-9599507
16	BHLHE40	chr1:9598963-9600458	K562	blood:	n/a	chr1:9599494-9599507
17	BHLHE40	chr1:9599112-9599719	HepG2	liver:	n/a	chr1:9599494-9599507
18	BHLHE40	chr1:9599271-9599670	HepG2	liver:	n/a	chr1:9599494-9599507
19	BRCA1	chr1:9599087-9599615	HepG2	liver:	n/a	n/a
20	BRCA1	chr1:9599058-9599449	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr1:9599087-9599547	GM12878	blood:	n/a	n/a
22	BRCA1	chr1:9599088-9599644	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr1:9600075-9600403	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr1:9598786-9599532	K562	blood:	n/a	n/a
25	CBX3	chr1:9599973-9600886	K562	blood:	n/a	n/a
26	CCNT2	chr1:9598904-9600430	K562	blood:	n/a	chr1:9600151-9600160 chr1:9600145-9600154
27	CEBPB	chr1:9599183-9599658	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:9599254-9599621	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:9599202-9599526	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:9599148-9599556	A549	lung:	n/a	n/a
31	CEBPB	chr1:9599189-9599561	A549	lung:	n/a	n/a
32	CEBPB	chr1:9599146-9599533	MCF-7	breast:	n/a	n/a
33	CEBPB	chr1:9599077-9599573	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:9599184-9599702	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:9599024-9599549	K562	blood:	n/a	n/a
36	CEBPB	chr1:9599148-9599497	K562	blood:	n/a	n/a
37	CEBPB	chr1:9599214-9599560	MCF-7	breast:	n/a	n/a
38	CEBPB	chr1:9596259-9596434	K562	blood:	n/a	n/a
39	CEBPB	chr1:9599172-9599569	K562	blood:	n/a	n/a
40	CEBPB	chr1:9599252-9599494	A549	lung:	n/a	n/a
41	CEBPB	chr1:9599193-9599517	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr1:9597942-9598250	HepG2	liver:	n/a	chr1:9598084-9598096
43	CEBPB	chr1:9599187-9599572	IMR90	lung:	n/a	n/a
44	CEBPD	chr1:9599208-9599656	HepG2	liver:	n/a	n/a
45	CEBPD	chr1:9597917-9598226	HepG2	liver:	n/a	n/a
46	CEBPD	chr1:9599368-9599666	HepG2	liver:	n/a	n/a
47	CEBPD	chr1:9598849-9599624	K562	blood:	n/a	n/a
48	CEBPD	chr1:9598043-9598407	HepG2	liver:	n/a	n/a
49	CHD1	chr1:9599968-9600277	GM12878	blood:	n/a	n/a
50	CHD2	chr1:9599996-9600369	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:9599026-9599076	T-47D	breast:	n/a
2	chr1:9600115-9600165	BJ	skin:	n/a
3	chr1:9599067-9599117	K562	blood:	n/a
4	chr1:9599067-9599117	HIPEpiC	eye:	n/a
5	chr1:9599276-9599326	HCT-116	colon:	n/a
6	chr1:9599067-9599117	PANC-1	pancreas:	n/a
7	chr1:9599403-9599453	ECC-1	luminal epithelium:	n/a
8	chr1:9599380-9599430	HCPEpiC	choroid plexus:	n/a
9	chr1:9599067-9599117	HMEC	breast:	n/a
10	chr1:9599380-9599430	BJ	skin:	n/a
11	chr1:9599256-9599306	NT2-D1	testis:	n/a
12	chr1:9598932-9598982	HL-60	blood:	n/a
13	chr1:9599380-9599430	T-47D	breast:	n/a
14	chr1:9599419-9599469	GM12891	blood:	n/a
15	chr1:9599256-9599306	HIPEpiC	eye:	n/a
16	chr1:9599256-9599306	LNCaP	prostate:	n/a
17	chr1:9599256-9599306	ECC-1	luminal epithelium:	n/a
18	chr1:9599674-9599724	AG09309	skin:	n/a
19	chr1:9599419-9599469	GM06990	blood:	n/a
20	chr1:9598983-9599033	SAEC	small airway:	n/a
21	chr1:9599067-9599117	GM06990	blood:	n/a
22	chr1:9600115-9600165	HRPEpiC	eye:	n/a
23	chr1:9599419-9599469	MCF10A-Er-Src	breast:	n/a
24	chr1:9599391-9599441	MCF-7	breast:	n/a
25	chr1:9598983-9599033	HUVEC	blood vessel:	n/a
26	chr1:9599419-9599469	HAEpiC	amniotic membrane:	n/a
27	chr1:9599380-9599430	HNPCEpiC	eye:	n/a
28	chr1:9598932-9598982	T-47D	breast:	n/a
29	chr1:9599401-9599451	PFSK-1	brain:	n/a
30	chr1:9599256-9599306	AG10803	skin:	n/a
31	chr1:9600115-9600165	RPTEC	kidney:	n/a
32	chr1:9599391-9599441	BJ	skin:	n/a
33	chr1:9599026-9599076	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:9599380-9599430	Caco-2	colon:	n/a
35	chr1:9599401-9599451	GM19239	blood:	n/a
36	chr1:9598932-9598982	GM12891	blood:	n/a
37	chr1:9599380-9599430	GM12891	blood:	n/a
38	chr1:9599419-9599469	Caco-2	colon:	n/a
39	chr1:9599401-9599451	HRPEpiC	eye:	n/a
40	chr1:9599276-9599326	GM12892	blood:	n/a
41	chr1:9599391-9599441	HCF	heart:	n/a
42	chr1:9599380-9599430	K562	blood:	n/a
43	chr1:9599674-9599724	HNPCEpiC	eye:	n/a
44	chr1:9600115-9600165	Jurkat	blood:	n/a
45	chr1:9599674-9599724	PFSK-1	brain:	n/a
46	chr1:9600115-9600165	AG09309	skin:	n/a
47	chr1:9598983-9599033	SKMC	muscle:	n/a
48	chr1:9598932-9598982	ECC-1	luminal epithelium:	n/a
49	chr1:9599380-9599430	A549	lung:	n/a
50	chr1:9599419-9599469	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:9599090..9600004-chr11:94964653..94965231,2	NB4	blood:
2	chr1:9593476..9595125-chr1:9597085..9600029,2	K562	blood:
3	chr1:9597781..9602686-chr1:9646599..9652829,9	K562	blood:
4	chr1:9589698..9594736-chr1:9596455..9600782,9	K562	blood:
5	chr1:9597734..9599433-chr1:9617661..9619736,2	K562	blood:
6	chr1:9588042..9590457-chr1:9592247..9594686,2	K562	blood:
7	chr1:9594978..9597511-chr1:9598166..9600611,4	K562	blood:
8	chr1:9350586..9353918-chr1:9597167..9600975,3	MCF-7	breast:
9	chr1:9596866..9598419-chr1:9883166..9885475,2	K562	blood:
10	chr1:9599563..9600515-chr15:65588090..65588719,2	Hela-S3	cervix:
11	chr1:9586876..9589181-chr1:9596662..9599409,2	K562	blood:
12	chr1:9340527..9342561-chr1:9591961..9594805,2	K562	blood:
13	chr1:9600120..9603287-chr1:9652178..9655376,3	K562	blood:
14	chr1:9599233..9600127-chr6:111279644..111280229,2	Hela-S3	cervix:
15	chr1:9294638..9296253-chr1:9598479..9600330,2	K562	blood:
16	chr1:9588957..9591794-chr1:9592247..9595158,3	K562	blood:
17	chr1:9599401..9600258-chr2:55277246..55277773,2	Hela-S3	cervix:
18	chr1:9599360..9599951-chr2:43453657..43454519,2	NB4	blood:
19	chr1:9599430..9599966-chr2:162164733..162165342,2	Hela-S3	cervix:
20	chr1:9599309..9599945-chr20:48599375..48600280,2	Hela-S3	cervix:
21	chr1:9594867..9596553-chr1:9616924..9619437,2	MCF-7	breast:
22	chr1:9599545..9601173-chr1:9607657..9610579,2	MCF-7	breast:
23	chr1:9597937..9599836-chr1:9648693..9652829,4	K562	blood:
24	chr1:9599460..9600393-chr11:92930413..92931236,2	NB4	blood:

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

Extended variants
information (count: 217 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:217 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535786008	chr1:9593581-9593582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536553094	chr1:9593610-9593611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557302203	chr1:9593651-9593652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs200138995	chr1:9593654-9593655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569125387	chr1:9593692-9593693	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs55780537	chr1:9593702-9593703	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558876031	chr1:9593717-9593718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs55986711	chr1:9593797-9593798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541494738	chr1:9593882-9593883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566519152	chr1:9593952-9593953	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534758245	chr1:9593995-9593996	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371294800	chr1:9594005-9594006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373334785	chr1:9594051-9594052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574682969	chr1:9594061-9594062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552928853	chr1:9594094-9594095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563644369	chr1:9594107-9594108	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531210814	chr1:9594111-9594112	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545499908	chr1:9594112-9594113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564085836	chr1:9594140-9594141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184493263	chr1:9594183-9594184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs144657787	chr1:9594195-9594196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568121533	chr1:9594228-9594229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12136603	chr1:9594278-9594279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs12136605	chr1:9594309-9594310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113476517	chr1:9594358-9594359	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550766412	chr1:9594402-9594403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs141257410	chr1:9594418-9594419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539706198	chr1:9594461-9594462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77048253	chr1:9594472-9594473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150759642	chr1:9594473-9594474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75315738	chr1:9594475-9594476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs79840762	chr1:9594483-9594484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs80198604	chr1:9594485-9594486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs61394664	chr1:9594534-9594535	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188858940	chr1:9594536-9594537	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534847176	chr1:9594537-9594538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs374685621	chr1:9594544-9594545	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs181200071	chr1:9594545-9594546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574547933	chr1:9594559-9594560	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs58416959	chr1:9594590-9594591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535676564	chr1:9594601-9594602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557101247	chr1:9594631-9594632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138093723	chr1:9594659-9594660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577537148	chr1:9594660-9594661	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12037667	chr1:9594670-9594671	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs553788378	chr1:9594671-9594672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572804138	chr1:9594766-9594767	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs540188615	chr1:9594787-9594788	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561788548	chr1:9594788-9594789	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376930168	chr1:9594792-9594793	Weak transcription	Chromatin interactive region	1 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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr1:9592200-9593600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr1:9592600-9593600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:9592600-9593600	Enhancers	Brain Hippocampus Middle	brain
10	chr1:9592600-9594400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr1:9592800-9593600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:9592800-9593600	Enhancers	Brain Substantia Nigra	brain
13	chr1:9592800-9593600	Enhancers	Fetal Intestine Large	intestine
14	chr1:9592800-9593600	Enhancers	Fetal Intestine Small	intestine
15	chr1:9592800-9594600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:9593000-9593600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr1:9593000-9593600	Enhancers	Brain Angular Gyrus	brain
18	chr1:9593000-9593600	Enhancers	Fetal Stomach	stomach
19	chr1:9593000-9593800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr1:9593200-9593600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:9593200-9593600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr1:9593200-9593600	Enhancers	Fetal Kidney	kidney
23	chr1:9593200-9598600	Weak transcription	Brain Anterior Caudate	brain
24	chr1:9593200-9599000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:9593400-9593800	Enhancers	HepG2	liver
26	chr1:9593400-9597800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr1:9593400-9597800	Weak transcription	Liver	Liver
28	chr1:9593400-9598000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:9593400-9598400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:9593400-9598600	Weak transcription	Fetal Lung	lung
31	chr1:9593400-9598800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr1:9593400-9598800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr1:9593400-9598800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr1:9593600-9596200	Weak transcription	Fetal Intestine Small	intestine
35	chr1:9593600-9597200	Weak transcription	Fetal Intestine Large	intestine
36	chr1:9593600-9598000	Weak transcription	Brain Substantia Nigra	brain
37	chr1:9593600-9598200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr1:9593600-9598200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:9593600-9598400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr1:9593600-9598800	Weak transcription	Brain Hippocampus Middle	brain
41	chr1:9593600-9599000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:9593600-9599000	Weak transcription	Brain Angular Gyrus	brain
43	chr1:9593600-9599600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:9593800-9596400	Weak transcription	HepG2	liver
45	chr1:9593800-9599000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr1:9594400-9599400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr1:9594600-9599000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:9595800-9596000	Enhancers	H9 Cell Line	embryonic stem cell
49	chr1:9596200-9596400	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr1:9596200-9597000	Enhancers	Fetal Intestine Small	intestine

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