Variant report

Variant	nsv870608
Chromosome Location	chr1:78520822-78594286
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:910)
CpG islands
(count:61)
Chromatin interactive
region (count:92)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:910 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:78580080-78580462	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:78580017-78580419	K562	blood:	n/a	n/a
3	ARID3A	chr1:78554741-78554986	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:78556964-78557193	K562	blood:	n/a	n/a
5	ARID3A	chr1:78554713-78554853	K562	blood:	n/a	n/a
6	ATF1	chr1:78550448-78550683	K562	blood:	n/a	n/a
7	ATF1	chr1:78556918-78557350	K562	blood:	n/a	n/a
8	ATF2	chr1:78526746-78527321	GM12878	blood:	n/a	n/a
9	ATF2	chr1:78536404-78536805	GM12878	blood:	n/a	n/a
10	ATF2	chr1:78526917-78527246	GM12878	blood:	n/a	n/a
11	ATF3	chr1:78580111-78580319	K562	blood:	n/a	n/a
12	ATF3	chr1:78560286-78560819	HCT-116	colon:	n/a	n/a
13	BACH1	chr1:78580189-78580226	K562	blood:	n/a	n/a
14	BACH1	chr1:78574523-78574534	K562	blood:	n/a	n/a
15	BACH1	chr1:78592719-78592724	K562	blood:	n/a	n/a
16	BATF	chr1:78526870-78527239	GM12878	blood:	n/a	chr1:78527046-78527057
17	BATF	chr1:78553783-78554011	GM12878	blood:	n/a	n/a
18	BATF	chr1:78553780-78553963	GM12878	blood:	n/a	n/a
19	BATF	chr1:78526837-78527275	GM12878	blood:	n/a	chr1:78527046-78527057
20	BATF	chr1:78536466-78536803	GM12878	blood:	n/a	chr1:78536751-78536759
21	BCL11A	chr1:78526869-78527227	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:78526847-78527243	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:78580045-78580379	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:78556899-78557501	K562	blood:	n/a	chr1:78557099-78557115
25	BHLHE40	chr1:78580054-78580292	K562	blood:	n/a	n/a
26	BHLHE40	chr1:78580176-78580406	HepG2	liver:	n/a	n/a
27	BRCA1	chr1:78558275-78558652	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr1:78536385-78536894	HCT-116	colon:	n/a	n/a
29	CBX3	chr1:78567089-78567795	HCT-116	colon:	n/a	n/a
30	CBX3	chr1:78567088-78567855	HCT-116	colon:	n/a	n/a
31	CBX3	chr1:78558278-78558770	HCT-116	colon:	n/a	n/a
32	CCNT2	chr1:78550403-78550638	K562	blood:	n/a	n/a
33	CCNT2	chr1:78556970-78557250	K562	blood:	n/a	n/a
34	CEBPB	chr1:78588148-78588481	H1-hESC	embryonic stem cell:	n/a	chr1:78588320-78588331
35	CEBPB	chr1:78559234-78559606	Hela-S3	cervix:	n/a	chr1:78559418-78559429 chr1:78559420-78559429
36	CEBPB	chr1:78559247-78559587	HepG2	liver:	n/a	chr1:78559418-78559429 chr1:78559420-78559429
37	CEBPB	chr1:78588197-78588506	HepG2	liver:	n/a	chr1:78588320-78588331
38	CEBPB	chr1:78559320-78559553	A549	lung:	n/a	chr1:78559418-78559429 chr1:78559420-78559429
39	CEBPB	chr1:78559293-78559553	K562	blood:	n/a	chr1:78559418-78559429 chr1:78559420-78559429
40	CEBPB	chr1:78536515-78536802	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:78559270-78559603	IMR90	lung:	n/a	chr1:78559418-78559429 chr1:78559420-78559429
42	CEBPB	chr1:78558230-78558770	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr1:78580208-78580247	K562	blood:	n/a	n/a
44	CEBPB	chr1:78521236-78521425	K562	blood:	n/a	n/a
45	CEBPB	chr1:78532549-78532768	A549	lung:	n/a	n/a
46	CEBPB	chr1:78588248-78588416	K562	blood:	n/a	chr1:78588320-78588331
47	CEBPB	chr1:78588203-78588478	IMR90	lung:	n/a	chr1:78588320-78588331
48	CEBPD	chr1:78556841-78557271	K562	blood:	n/a	n/a
49	CEBPD	chr1:78550361-78550721	K562	blood:	n/a	n/a
50	CHD1	chr1:78579491-78580673	IMR90	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:78567723-78567773	K562	blood:	n/a
2	chr1:78567723-78567773	HNPCEpiC	eye:	n/a
3	chr1:78567723-78567773	HMEC	breast:	n/a
4	chr1:78567723-78567773	SK-N-MC	brain:	n/a
5	chr1:78567723-78567773	RPTEC	kidney:	n/a
6	chr1:78567723-78567773	SK-N-SH_RA	brain:	n/a
7	chr1:78567723-78567773	PFSK-1	brain:	n/a
8	chr1:78567723-78567773	HL-60	blood:	n/a
9	chr1:78567723-78567773	PrEC	prostate:	n/a
10	chr1:78567723-78567773	AoSMC	blood vessel:	n/a
11	chr1:78567723-78567773	AG09319	gingival:	n/a
12	chr1:78567723-78567773	AG04450	lung:	fetal
13	chr1:78567723-78567773	SKMC	muscle:	n/a
14	chr1:78567723-78567773	CMK	blood:	n/a
15	chr1:78567723-78567773	GM19239	blood:	n/a
16	chr1:78567723-78567773	HepG2	liver:	n/a
17	chr1:78567723-78567773	AG09309	skin:	n/a
18	chr1:78567723-78567773	AG10803	skin:	n/a
19	chr1:78567723-78567773	H1-hESC	embryonic stem cell:	embryo
20	chr1:78567723-78567773	HCT-116	colon:	n/a
21	chr1:78567723-78567773	NH-A	brain:	n/a
22	chr1:78567723-78567773	GM12892	blood:	n/a
23	chr1:78567723-78567773	NT2-D1	testis:	n/a
24	chr1:78567723-78567773	SK-N-SH	brain:	n/a
25	chr1:78567723-78567773	HCM	heart:	n/a
26	chr1:78567723-78567773	NHDF-neo	bronchial:	n/a
27	chr1:78567723-78567773	ovcar-3	ovarian:	n/a
28	chr1:78567723-78567773	PANC-1	pancreas:	n/a
29	chr1:78567723-78567773	LNCaP	prostate:	n/a
30	chr1:78567723-78567773	ECC-1	luminal epithelium:	n/a
31	chr1:78567723-78567773	HRPEpiC	eye:	n/a
32	chr1:78567723-78567773	AG04449	skin:	fetal
33	chr1:78567723-78567773	HRCEpiC	kidney:	n/a
34	chr1:78567723-78567773	HRE	kidney:	n/a
35	chr1:78567723-78567773	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:78567723-78567773	ProgFib	skin:	n/a
37	chr1:78567723-78567773	Jurkat	blood:	n/a
38	chr1:78567723-78567773	BJ	skin:	n/a
39	chr1:78567723-78567773	A549	lung:	n/a
40	chr1:78567723-78567773	NHBE	bronchial:	n/a
41	chr1:78567723-78567773	MCF10A-Er-Src	breast:	n/a
42	chr1:78567723-78567773	NB4	blood:	n/a
43	chr1:78567723-78567773	HEK293	kidney:	embryo
44	chr1:78567723-78567773	Hela-S3	cervix:	n/a
45	chr1:78567723-78567773	HCF	heart:	n/a
46	chr1:78567723-78567773	HUVEC	blood vessel:	n/a
47	chr1:78567723-78567773	HCPEpiC	choroid plexus:	n/a
48	chr1:78567723-78567773	BE2_C	brain:	n/a
49	chr1:78567723-78567773	GM06990	blood:	n/a
50	chr1:78567723-78567773	Caco-2	colon:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:78555766..78558771-chr1:78559495..78562438,3	K562	blood:
2	chr1:78520206..78525011-chr1:78526646..78528908,4	K562	blood:
3	chr1:78580164..78582715-chr1:78584966..78587634,2	K562	blood:
4	chr1:78538964..78540901-chr1:78545942..78548029,2	K562	blood:
5	chr1:78468803..78471404-chr1:78570438..78572886,2	K562	blood:
6	chr1:78468395..78470223-chr1:78565706..78567712,2	K562	blood:
7	chr1:78518422..78519997-chr1:78524033..78526694,2	K562	blood:
8	chr1:78473290..78475127-chr1:78557271..78559371,2	K562	blood:
9	chr1:78475214..78476782-chr1:78520610..78522238,2	K562	blood:
10	chr1:78484921..78487843-chr1:78526305..78528033,2	K562	blood:
11	chr1:78460274..78462084-chr1:78542241..78544116,2	MCF-7	breast:
12	chr1:78545378..78547879-chr1:78549298..78551293,2	K562	blood:
13	chr1:78563137..78565302-chr1:78567151..78570075,2	K562	blood:
14	chr1:78589424..78592317-chr1:78594735..78598058,3	K562	blood:
15	chr1:78467270..78470247-chr1:78561898..78563646,2	MCF-7	breast:
16	chr1:78442786..78443510-chr1:78579652..78580579,4	MCF-7	breast:
17	chr1:78571357..78574328-chr1:78583197..78584874,2	K562	blood:
18	chr1:78474587..78476658-chr1:78580755..78582747,2	K562	blood:
19	chr1:78544669..78546952-chr1:85187355..85190224,2	K562	blood:
20	chr1:78541840..78545683-chr1:78546153..78548591,3	K562	blood:
21	chr1:78594062..78596652-chr1:78598664..78601035,2	K562	blood:
22	chr1:78482811..78485381-chr1:78578750..78581100,2	K562	blood:
23	chr1:78557581..78562861-chr1:78563464..78569701,7	K562	blood:
24	chr1:78521484..78522081-chr1:78580194..78580696,2	MCF-7	breast:
25	chr1:78580164..78582715-chr1:78584966..78587634,2	K562	blood:
26	chr1:78468498..78473309-chr1:78543604..78549823,9	K562	blood:
27	chr1:78563137..78565302-chr1:78567151..78570075,2	K562	blood:
28	chr1:78521484..78522081-chr1:78580194..78580696,2	MCF-7	breast:
29	chr1:78444622..78445852-chr1:78579780..78580682,4	MCF-7	breast:
30	chr1:78414449..78415158-chr1:78579807..78580633,3	MCF-7	breast:
31	chr1:78443664..78446688-chr1:78530483..78532507,3	K562	blood:
32	chr1:77613628..77614149-chr1:78580241..78580790,2	K562	blood:
33	chr1:78469091..78471508-chr1:78586744..78589573,2	K562	blood:
34	chr1:78534641..78538084-chr1:78538744..78543341,4	K562	blood:
35	chr1:78566289..78569501-chr1:78570769..78573554,3	K562	blood:
36	chr1:78390813..78392462-chr1:78574866..78577116,2	K562	blood:
37	chr1:78545378..78547879-chr1:78549298..78551293,2	K562	blood:
38	chr1:78571357..78574328-chr1:78583197..78584874,2	K562	blood:
39	chr1:78555766..78558771-chr1:78559495..78562438,3	K562	blood:
40	chr1:78593850..78595901-chr1:78596317..78598534,2	K562	blood:
41	chr1:78565458..78567789-chr1:78569626..78572269,2	K562	blood:
42	chr1:78534416..78536701-chr1:78562290..78564731,2	K562	blood:
43	chr1:78441362..78443969-chr1:78545013..78547502,2	K562	blood:
44	chr1:78544183..78545976-chr1:78546306..78547975,2	K562	blood:
45	chr1:78472783..78474858-chr1:78555582..78557141,2	K562	blood:
46	chr1:78467407..78471313-chr1:78589866..78593513,3	K562	blood:
47	chr1:78468333..78471378-chr1:78560977..78563691,3	K562	blood:
48	chr1:78468499..78472700-chr1:78534079..78541186,10	K562	blood:
49	chr1:78467407..78471313-chr1:78589866..78593513,4	K562	blood:
50	chr1:78544325..78546511-chr1:78564986..78567853,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-1102P	TF binding region
ENSG00000213560	TF binding region
RNA5SP22	TF binding region
RNU6-1102P	CpG island
ENSG00000213560	CpG island
RNA5SP22	CpG island
ENSG00000162614	chromatin interactions
ENSG00000213560	chromatin interactions
ENSG00000162613	chromatin interactions
ENSG00000202263	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000137960	chromatin interactions
ENSG00000273338	chromatin interactions

Extended variants
information (count: 2500 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2500 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12067638	chr1:78520822-78520823	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569430010	chr1:78520947-78520948	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs7514007	chr1:78520983-78520984	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs370155328	chr1:78521097-78521098	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs555626620	chr1:78521114-78521115	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs373326069	chr1:78521174-78521175	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs566752460	chr1:78521178-78521179	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs567446043	chr1:78521205-78521206	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs374763504	chr1:78521211-78521212	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs187868309	chr1:78521285-78521286	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs191835572	chr1:78521288-78521289	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs182791314	chr1:78521300-78521301	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs71641320	chr1:78521313-78521314	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs538860406	chr1:78521385-78521386	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs141414996	chr1:78521413-78521414	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs555237604	chr1:78521462-78521463	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs576636099	chr1:78521480-78521481	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs572170954	chr1:78521499-78521500	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs76877249	chr1:78521561-78521562	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs562153379	chr1:78521577-78521578	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs115016425	chr1:78521582-78521583	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs541662429	chr1:78521587-78521588	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs559816264	chr1:78521694-78521695	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs113357283	chr1:78521704-78521705	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs533316707	chr1:78521740-78521741	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs551594820	chr1:78521744-78521745	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563022774	chr1:78521748-78521749	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs6669039	chr1:78521765-78521766	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs187435839	chr1:78521795-78521796	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs7523750	chr1:78521815-78521816	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs528079242	chr1:78521868-78521869	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs11162410	chr1:78521931-78521932	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571597538	chr1:78521970-78521971	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577758068	chr1:78522139-78522140	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538813171	chr1:78522140-78522141	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs373414834	chr1:78522165-78522166	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs549425688	chr1:78522171-78522172	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375880828	chr1:78522175-78522176	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs192329396	chr1:78522199-78522200	Weak transcription Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs529579298	chr1:78522215-78522216	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs540228988	chr1:78522231-78522232	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553775787	chr1:78522246-78522247	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs570152724	chr1:78522269-78522270	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs185511405	chr1:78522321-78522322	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373688180	chr1:78522363-78522364	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs537510849	chr1:78522427-78522428	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs140549175	chr1:78522432-78522433	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573949841	chr1:78522498-78522499	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376663995	chr1:78522589-78522590	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs12125903	chr1:78522625-78522626	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	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
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	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
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	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
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78513000-78521800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:78513600-78521200	Weak transcription	Stomach Mucosa	stomach
3	chr1:78515400-78521200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr1:78515400-78534200	Weak transcription	HepG2	liver
5	chr1:78517400-78522000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr1:78517800-78521200	Weak transcription	Fetal Intestine Small	intestine
7	chr1:78519000-78521000	Weak transcription	Adipose Nuclei	Adipose
8	chr1:78519000-78521400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:78519000-78536000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:78519200-78521000	Weak transcription	Fetal Intestine Large	intestine
11	chr1:78519200-78527000	Weak transcription	Fetal Muscle Leg	muscle
12	chr1:78519400-78521200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr1:78519400-78521200	Weak transcription	Small Intestine	intestine
14	chr1:78519400-78521200	Weak transcription	K562	blood
15	chr1:78519400-78521400	Weak transcription	Placenta	Placenta
16	chr1:78519400-78521400	Weak transcription	Right Atrium	heart
17	chr1:78519400-78521400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr1:78519800-78526800	Weak transcription	Psoas Muscle	Psoas
19	chr1:78520000-78521000	Enhancers	HSMM	muscle
20	chr1:78520000-78521400	Enhancers	HUVEC	blood vessel
21	chr1:78520400-78521400	Enhancers	Liver	Liver
22	chr1:78520600-78522000	Enhancers	Pancreas	Pancrea
23	chr1:78520600-78522000	Enhancers	Spleen	Spleen
24	chr1:78520800-78521800	Enhancers	Right Ventricle	heart
25	chr1:78520800-78522000	Enhancers	Left Ventricle	heart
26	chr1:78520800-78523800	Weak transcription	Osteobl	bone
27	chr1:78520800-78524000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr1:78520800-78526600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:78520800-78526800	Weak transcription	HSMMtube	muscle
30	chr1:78521000-78521200	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr1:78521000-78521200	Active TSS	Rectal Mucosa Donor 31	rectum
32	chr1:78521000-78521600	Enhancers	Fetal Intestine Large	intestine
33	chr1:78521000-78524200	Weak transcription	HSMM	muscle
34	chr1:78521200-78521400	Enhancers	K562	blood
35	chr1:78521200-78521600	Enhancers	Colonic Mucosa	Colon
36	chr1:78521200-78521600	Flanking Active TSS	Duodenum Mucosa	Duodenum
37	chr1:78521200-78521600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
38	chr1:78521200-78521600	Enhancers	Stomach Mucosa	stomach
39	chr1:78521200-78521600	Enhancers	HMEC	breast
40	chr1:78521200-78521800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:78521200-78521800	Enhancers	Fetal Intestine Small	intestine
42	chr1:78521200-78521800	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr1:78521200-78521800	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr1:78521200-78522000	Active TSS	Adipose Nuclei	Adipose
45	chr1:78521200-78522200	Enhancers	Small Intestine	intestine
46	chr1:78521400-78521600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:78521400-78521600	Enhancers	Right Atrium	heart
48	chr1:78521400-78521800	Flanking Active TSS	Liver	Liver
49	chr1:78521400-78521800	Active TSS	Duodenum Smooth Muscle	Duodenum
50	chr1:78521400-78521800	Enhancers	Placenta	Placenta

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