Variant report

Variant	nsv1016788
Chromosome Location	chr6:34496002-34529165
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:874)
CpG islands
(count:1648)
Chromatin interactive
region (count:108)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34528321-34529035	K562	blood:	n/a	n/a
2	ARID3A	chr6:34528420-34528567	HepG2	liver:	n/a	n/a
3	ATF1	chr6:34528256-34528770	K562	blood:	n/a	n/a
4	ATF1	chr6:34498693-34498808	K562	blood:	n/a	n/a
5	BACH1	chr6:34528081-34528565	K562	blood:	n/a	n/a
6	BACH1	chr6:34525098-34525122	K562	blood:	n/a	n/a
7	BCL3	chr6:34522693-34523062	GM12878	blood:	n/a	n/a
8	BCL3	chr6:34522720-34523036	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:34526077-34526348	K562	blood:	n/a	n/a
10	BHLHE40	chr6:34512632-34512964	K562	blood:	n/a	n/a
11	BHLHE40	chr6:34525097-34525230	K562	blood:	n/a	n/a
12	BHLHE40	chr6:34498559-34498914	K562	blood:	n/a	n/a
13	BHLHE40	chr6:34528358-34529016	HepG2	liver:	n/a	n/a
14	BHLHE40	chr6:34527683-34529135	K562	blood:	n/a	n/a
15	BRCA1	chr6:34528383-34528433	HepG2	liver:	n/a	n/a
16	BRCA1	chr6:34528656-34528787	HepG2	liver:	n/a	n/a
17	CBX3	chr6:34512311-34513045	K562	blood:	n/a	n/a
18	CBX3	chr6:34524227-34524720	K562	blood:	n/a	n/a
19	CBX3	chr6:34504652-34505107	K562	blood:	n/a	n/a
20	CBX3	chr6:34504717-34505022	K562	blood:	n/a	n/a
21	CBX3	chr6:34528238-34529132	K562	blood:	n/a	n/a
22	CBX3	chr6:34528147-34529296	K562	blood:	n/a	n/a
23	CBX3	chr6:34525886-34526725	K562	blood:	n/a	n/a
24	CBX3	chr6:34499300-34499739	K562	blood:	n/a	n/a
25	CBX3	chr6:34498382-34499182	K562	blood:	n/a	n/a
26	CBX3	chr6:34525771-34526610	K562	blood:	n/a	n/a
27	CCNT2	chr6:34519480-34519561	K562	blood:	n/a	n/a
28	CCNT2	chr6:34524999-34525293	K562	blood:	n/a	n/a
29	CCNT2	chr6:34512678-34512912	K562	blood:	n/a	n/a
30	CCNT2	chr6:34528207-34528986	K562	blood:	n/a	chr6:34528756-34528765
31	CEBPB	chr6:34512433-34512769	IMR90	lung:	n/a	chr6:34512601-34512612
32	CEBPB	chr6:34512498-34512758	H1-hESC	embryonic stem cell:	n/a	chr6:34512601-34512612
33	CEBPB	chr6:34497425-34497656	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr6:34512412-34512961	K562	blood:	n/a	chr6:34512601-34512612
35	CEBPB	chr6:34512507-34512661	K562	blood:	n/a	chr6:34512601-34512612
36	CEBPB	chr6:34528245-34528702	K562	blood:	n/a	n/a
37	CEBPB	chr6:34512444-34512756	A549	lung:	n/a	chr6:34512601-34512612
38	CEBPB	chr6:34512441-34512760	HepG2	liver:	n/a	chr6:34512601-34512612
39	CEBPB	chr6:34528488-34528675	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:34512447-34512874	K562	blood:	n/a	chr6:34512601-34512612
41	CEBPB	chr6:34504268-34505039	MCF-7	breast:	n/a	n/a
42	CEBPD	chr6:34512514-34513045	K562	blood:	n/a	n/a
43	CEBPD	chr6:34524939-34525496	K562	blood:	n/a	n/a
44	CEBPD	chr6:34528208-34528720	K562	blood:	n/a	n/a
45	CEBPD	chr6:34524892-34525479	K562	blood:	n/a	n/a
46	CHD2	chr6:34524902-34525076	K562	blood:	n/a	n/a
47	CHD2	chr6:34528783-34528794	HepG2	liver:	n/a	n/a
48	CHD2	chr6:34499540-34499799	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr6:34499393-34499717	K562	blood:	n/a	n/a
50	CHD2	chr6:34528258-34528859	K562	blood:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34525026-34525076	GM12878	blood:	n/a
2	chr6:34525026-34525076	GM12878	blood:	n/a
3	chr6:34512083-34512133	HMEC	breast:	n/a
4	chr6:34525026-34525076	GM19239	blood:	n/a
5	chr6:34499389-34499439	SK-N-SH_RA	brain:	n/a
6	chr6:34524278-34524328	Caco-2	colon:	n/a
7	chr6:34502119-34502169	AG10803	skin:	n/a
8	chr6:34512083-34512133	PrEC	prostate:	n/a
9	chr6:34513187-34513237	SAEC	small airway:	n/a
10	chr6:34512083-34512133	AG10803	skin:	n/a
11	chr6:34514887-34514937	ECC-1	luminal epithelium:	n/a
12	chr6:34512083-34512133	HRPEpiC	eye:	n/a
13	chr6:34525026-34525076	H1-hESC	embryonic stem cell:	embryo
14	chr6:34513187-34513237	AG10803	skin:	n/a
15	chr6:34504890-34504940	NHBE	bronchial:	n/a
16	chr6:34524095-34524145	HL-60	blood:	n/a
17	chr6:34512083-34512133	NB4	blood:	n/a
18	chr6:34499314-34499364	BE2_C	brain:	n/a
19	chr6:34502119-34502169	H1-hESC	embryonic stem cell:	embryo
20	chr6:34524095-34524145	Caco-2	colon:	n/a
21	chr6:34501193-34501243	GM12878	blood:	n/a
22	chr6:34525026-34525076	AG10803	skin:	n/a
23	chr6:34499314-34499364	LNCaP	prostate:	n/a
24	chr6:34499504-34499554	Hela-S3	cervix:	n/a
25	chr6:34524097-34524147	A549	lung:	n/a
26	chr6:34525026-34525076	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:34523925-34523975	Caco-2	colon:	n/a
28	chr6:34512215-34512265	BE2_C	brain:	n/a
29	chr6:34499504-34499554	HCM	heart:	n/a
30	chr6:34524766-34524816	GM06990	blood:	n/a
31	chr6:34512253-34512303	HUVEC	blood vessel:	n/a
32	chr6:34524698-34524748	HAEpiC	amniotic membrane:	n/a
33	chr6:34523925-34523975	HepG2	liver:	n/a
34	chr6:34524597-34524647	PrEC	prostate:	n/a
35	chr6:34528827-34528877	H1-hESC	embryonic stem cell:	embryo
36	chr6:34524290-34524340	SK-N-SH	brain:	n/a
37	chr6:34504890-34504940	NHDF-neo	bronchial:	n/a
38	chr6:34499488-34499538	HCF	heart:	n/a
39	chr6:34514887-34514937	NH-A	brain:	n/a
40	chr6:34511514-34511564	HAEpiC	amniotic membrane:	n/a
41	chr6:34524597-34524647	GM12891	blood:	n/a
42	chr6:34511514-34511564	AoSMC	blood vessel:	n/a
43	chr6:34524597-34524647	HIPEpiC	eye:	n/a
44	chr6:34499314-34499364	PrEC	prostate:	n/a
45	chr6:34499389-34499439	HRPEpiC	eye:	n/a
46	chr6:34499314-34499364	SKMC	muscle:	n/a
47	chr6:34524597-34524647	BE2_C	brain:	n/a
48	chr6:34499488-34499538	PANC-1	pancreas:	n/a
49	chr6:34513187-34513237	SK-N-SH	brain:	n/a
50	chr6:34501193-34501243	PrEC	prostate:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:34432385..34434700-chr6:34511007..34512543,2	MCF-7	breast:
2	chr6:34528717..34530463-chr6:34574776..34577421,2	K562	blood:
3	chr6:34497355..34498033-chr6:34557195..34557723,2	MCF-7	breast:
4	chr6:34495305..34497309-chr6:34500179..34501973,2	K562	blood:
5	chr6:34512842..34514603-chr6:34573896..34576620,2	MCF-7	breast:
6	chr20:52484501..52486317-chr6:34526583..34529198,2	MCF-7	breast:
7	chr6:34496034..34498791-chr6:34510835..34512433,2	K562	blood:
8	chr6:34392242..34394733-chr6:34507409..34509642,2	MCF-7	breast:
9	chr6:34527602..34533050-chr6:34533572..34539589,8	K562	blood:
10	chr6:34508607..34511346-chr6:34567639..34570139,2	K562	blood:
11	chr6:34495305..34497309-chr6:34500179..34501973,2	K562	blood:
12	chr6:34494038..34495878-chr6:34511727..34514586,2	K562	blood:
13	chr6:34496972..34497706-chr6:34576720..34577905,3	MCF-7	breast:
14	chr6:34391920..34394016-chr6:34508628..34510815,2	MCF-7	breast:
15	chr6:34494608..34496228-chr6:34576974..34578003,14	K562	blood:
16	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
17	chr6:34504144..34505003-chr6:34514225..34514901,2	MCF-7	breast:
18	chr6:34506980..34511719-chr6:34518115..34520438,4	K562	blood:
19	chr6:34501585..34503222-chr6:34504276..34506644,2	K562	blood:
20	chr6:34382272..34384689-chr6:34494911..34496600,2	K562	blood:
21	chr6:34508361..34510823-chr6:34510978..34513076,2	MCF-7	breast:
22	chr6:34501160..34503078-chr6:34510332..34511859,2	K562	blood:
23	chr6:34490255..34493000-chr6:34512065..34514942,2	K562	blood:
24	chr6:32936553..32938765-chr6:34521756..34523748,2	MCF-7	breast:
25	chr6:34494545..34497462-chr6:34498275..34503019,6	MCF-7	breast:
26	chr6:34204520..34207436-chr6:34522666..34524361,2	K562	blood:
27	chr6:34514003..34515621-chr6:34528599..34531450,2	K562	blood:
28	chr6:34427418..34428084-chr6:34497140..34498209,3	MCF-7	breast:
29	chr6:34495679..34498360-chr6:34503054..34505628,3	MCF-7	breast:
30	chr6:34524749..34526335-chr6:34530684..34532317,2	K562	blood:
31	chr6:34503239..34505474-chr6:34519140..34521426,2	MCF-7	breast:
32	chr6:34502654..34506400-chr6:34510960..34515406,9	MCF-7	breast:
33	chr6:34497242..34499881-chr6:34564591..34566557,2	MCF-7	breast:
34	chr6:34514736..34516500-chr6:34519380..34521095,2	K562	blood:
35	chr6:34522438..34524089-chr6:34549801..34552822,3	MCF-7	breast:
36	chr6:34505107..34506692-chr6:34515801..34518168,2	MCF-7	breast:
37	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
38	chr6:33686485..33689308-chr6:34514444..34516167,2	MCF-7	breast:
39	chr6:34495679..34498360-chr6:34503054..34505628,3	MCF-7	breast:
40	chr6:34427383..34427978-chr6:34528004..34528902,2	MCF-7	breast:
41	chr6:34426702..34428652-chr6:34520960..34523550,2	MCF-7	breast:
42	chr6:34514736..34516500-chr6:34519380..34521095,2	K562	blood:
43	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
44	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
45	chr6:34527129..34530623-chr6:34530939..34533511,3	K562	blood:
46	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
47	chr6:34500365..34503301-chr6:34563391..34565656,2	K562	blood:
48	chr6:34496034..34498791-chr6:34510835..34512433,2	K562	blood:
49	chr6:34503128..34505845-chr6:34536309..34539232,2	K562	blood:
50	chr6:34215456..34217891-chr6:34507762..34509808,2	K562	blood:

No data

Variant related genes	Relation type
SPDEF	TF binding region
SPDEF	CpG island
ENSG00000221635	chromatin interactions
ENSG00000124664	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000124507	chromatin interactions
ENSG00000196114	chromatin interactions
ENSG00000186577	chromatin interactions

Extended variants
information (count: 1433 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1433 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs59778290	chr6:34496014-34496015	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114901408	chr6:34496059-34496060	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs140644719	chr6:34496071-34496072	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs561206610	chr6:34496080-34496081	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs368273334	chr6:34496114-34496115	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs540922961	chr6:34496130-34496131	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs562110398	chr6:34496157-34496158	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs115556929	chr6:34496171-34496172	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs386700076	chr6:34496174-34496175	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs568591876	chr6:34496175-34496176	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs111252578	chr6:34496179-34496180	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs532911152	chr6:34496203-34496204	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs550953745	chr6:34496211-34496212	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs11755909	chr6:34496239-34496240	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs375818481	chr6:34496243-34496244	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs370177862	chr6:34496250-34496251	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs555656687	chr6:34496277-34496278	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs533766747	chr6:34496305-34496306	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs553516587	chr6:34496340-34496341	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs567483305	chr6:34496362-34496363	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs201843830	chr6:34496376-34496377	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs372896925	chr6:34496382-34496383	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs540470420	chr6:34496471-34496472	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs374966564	chr6:34496473-34496474	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs201050007	chr6:34496498-34496499	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs192786048	chr6:34496509-34496510	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs372665671	chr6:34496513-34496514	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs183923185	chr6:34496555-34496556	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs111572744	chr6:34496561-34496562	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs368944518	chr6:34496588-34496589	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs373996594	chr6:34496594-34496595	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs146300537	chr6:34496601-34496602	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs371006157	chr6:34496651-34496652	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs558135547	chr6:34496676-34496677	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs370850796	chr6:34496686-34496687	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs573209475	chr6:34496690-34496691	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs540533288	chr6:34496709-34496710	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs562393363	chr6:34496722-34496723	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs529590246	chr6:34496751-34496752	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs76107911	chr6:34496780-34496781	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs544400963	chr6:34496836-34496837	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs542786083	chr6:34496860-34496861	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs571296996	chr6:34496884-34496885	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs551065841	chr6:34496921-34496922	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs189050388	chr6:34496932-34496933	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs79659264	chr6:34497022-34497023	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs548730291	chr6:34497074-34497075	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs75017364	chr6:34497079-34497080	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs200674273	chr6:34497105-34497106	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs34502423	chr6:34497158-34497159	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34495000-34496200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:34495000-34504000	Weak transcription	Fetal Brain Male	brain
3	chr6:34495400-34496400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr6:34495400-34496400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:34495400-34496600	Enhancers	H1 Cell Line	embryonic stem cell
6	chr6:34495400-34496800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:34495400-34497200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:34495400-34497200	Weak transcription	Colonic Mucosa	Colon
9	chr6:34495400-34497200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr6:34495400-34497200	Weak transcription	Fetal Brain Female	brain
11	chr6:34495400-34497200	Weak transcription	Gastric	stomach
12	chr6:34495400-34497400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr6:34495400-34497600	Weak transcription	Lung	lung
14	chr6:34495400-34497600	Weak transcription	Pancreas	Pancrea
15	chr6:34495400-34497600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr6:34495400-34497600	Weak transcription	Right Ventricle	heart
17	chr6:34495400-34499200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr6:34495400-34499200	Weak transcription	Ovary	ovary
19	chr6:34495400-34501200	Weak transcription	Spleen	Spleen
20	chr6:34495400-34502000	Weak transcription	HSMMtube	muscle
21	chr6:34495400-34503000	Weak transcription	Brain Angular Gyrus	brain
22	chr6:34495400-34503800	Weak transcription	Brain Substantia Nigra	brain
23	chr6:34495400-34504200	Weak transcription	Left Ventricle	heart
24	chr6:34495400-34504600	Weak transcription	Right Atrium	heart
25	chr6:34495400-34506600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr6:34495600-34496200	Enhancers	K562	blood
27	chr6:34495600-34496600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:34495600-34497200	Weak transcription	Liver	Liver
29	chr6:34495600-34497200	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr6:34495600-34499000	Weak transcription	Fetal Thymus	thymus
31	chr6:34495600-34499200	Weak transcription	Primary B cells from peripheral blood	blood
32	chr6:34495600-34499200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr6:34495600-34499200	Weak transcription	Fetal Intestine Small	intestine
34	chr6:34495800-34496200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr6:34495800-34496200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr6:34495800-34496200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:34495800-34496200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr6:34495800-34497600	Weak transcription	Brain Germinal Matrix	brain
39	chr6:34495800-34499000	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr6:34495800-34499200	Weak transcription	Fetal Kidney	kidney
41	chr6:34495800-34503000	Weak transcription	Brain Anterior Caudate	brain
42	chr6:34495800-34503800	Weak transcription	Fetal Lung	lung
43	chr6:34495800-34505200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr6:34496000-34496200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr6:34496000-34496200	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr6:34496000-34497200	Weak transcription	Fetal Heart	heart
47	chr6:34496000-34497400	Weak transcription	A549	lung
48	chr6:34496000-34499200	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr6:34496200-34498200	Weak transcription	K562	blood
50	chr6:34496200-34498800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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