Variant report

Variant	nsv1032763
Chromosome Location	chr6:34509776-34552797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1265)
CpG islands
(count:1103)
Chromatin interactive
region (count:110)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34535143-34535361	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34528420-34528567	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:34537168-34537342	K562	blood:	n/a	n/a
4	ARID3A	chr6:34530717-34531006	K562	blood:	n/a	n/a
5	ARID3A	chr6:34528321-34529035	K562	blood:	n/a	n/a
6	ATF1	chr6:34528256-34528770	K562	blood:	n/a	n/a
7	ATF1	chr6:34530640-34531020	K562	blood:	n/a	n/a
8	BACH1	chr6:34528081-34528565	K562	blood:	n/a	n/a
9	BACH1	chr6:34525098-34525122	K562	blood:	n/a	n/a
10	BCL3	chr6:34543140-34543668	K562	blood:	n/a	chr6:34543350-34543359
11	BCL3	chr6:34522693-34523062	GM12878	blood:	n/a	n/a
12	BCL3	chr6:34522720-34523036	GM12878	blood:	n/a	n/a
13	BCL3	chr6:34541372-34541610	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:34530292-34531071	K562	blood:	n/a	n/a
15	BHLHE40	chr6:34528358-34529016	HepG2	liver:	n/a	n/a
16	BHLHE40	chr6:34526077-34526348	K562	blood:	n/a	n/a
17	BHLHE40	chr6:34535821-34536274	HepG2	liver:	n/a	n/a
18	BHLHE40	chr6:34527683-34529135	K562	blood:	n/a	n/a
19	BHLHE40	chr6:34525097-34525230	K562	blood:	n/a	n/a
20	BHLHE40	chr6:34512632-34512964	K562	blood:	n/a	n/a
21	BHLHE40	chr6:34531305-34531454	K562	blood:	n/a	n/a
22	BHLHE40	chr6:34535812-34536294	K562	blood:	n/a	n/a
23	BRCA1	chr6:34534813-34534889	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr6:34528656-34528787	HepG2	liver:	n/a	n/a
25	BRCA1	chr6:34528383-34528433	HepG2	liver:	n/a	n/a
26	BRCA1	chr6:34539475-34539630	HepG2	liver:	n/a	n/a
27	CBX3	chr6:34528238-34529132	K562	blood:	n/a	n/a
28	CBX3	chr6:34536960-34537774	K562	blood:	n/a	n/a
29	CBX3	chr6:34525771-34526610	K562	blood:	n/a	n/a
30	CBX3	chr6:34540332-34540766	K562	blood:	n/a	n/a
31	CBX3	chr6:34529829-34530430	K562	blood:	n/a	n/a
32	CBX3	chr6:34528147-34529296	K562	blood:	n/a	n/a
33	CBX3	chr6:34524227-34524720	K562	blood:	n/a	n/a
34	CBX3	chr6:34540358-34540680	K562	blood:	n/a	n/a
35	CBX3	chr6:34512311-34513045	K562	blood:	n/a	n/a
36	CBX3	chr6:34530537-34531593	K562	blood:	n/a	n/a
37	CBX3	chr6:34525886-34526725	K562	blood:	n/a	n/a
38	CCNT2	chr6:34524999-34525293	K562	blood:	n/a	n/a
39	CCNT2	chr6:34519480-34519561	K562	blood:	n/a	n/a
40	CCNT2	chr6:34528207-34528986	K562	blood:	n/a	chr6:34528756-34528765
41	CCNT2	chr6:34530372-34531113	K562	blood:	n/a	n/a
42	CCNT2	chr6:34535428-34535454	K562	blood:	n/a	n/a
43	CCNT2	chr6:34551355-34551428	K562	blood:	n/a	n/a
44	CCNT2	chr6:34512678-34512912	K562	blood:	n/a	n/a
45	CEBPB	chr6:34512444-34512756	A549	lung:	n/a	chr6:34512601-34512612
46	CEBPB	chr6:34512441-34512760	HepG2	liver:	n/a	chr6:34512601-34512612
47	CEBPB	chr6:34535856-34536113	HepG2	liver:	n/a	chr6:34535938-34535949
48	CEBPB	chr6:34535818-34536115	K562	blood:	n/a	chr6:34535938-34535949
49	CEBPB	chr6:34512498-34512758	H1-hESC	embryonic stem cell:	n/a	chr6:34512601-34512612
50	CEBPB	chr6:34512447-34512874	K562	blood:	n/a	chr6:34512601-34512612

(count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34525026-34525076	NT2-D1	testis:	n/a
2	chr6:34524698-34524748	HUVEC	blood vessel:	n/a
3	chr6:34524766-34524816	HEEpiC	esophagus:	n/a
4	chr6:34535602-34535652	K562	blood:	n/a
5	chr6:34524290-34524340	CMK	blood:	n/a
6	chr6:34525026-34525076	NT2-D1	testis:	n/a
7	chr6:34524698-34524748	HUVEC	blood vessel:	n/a
8	chr6:34524766-34524816	HEEpiC	esophagus:	n/a
9	chr6:34535602-34535652	K562	blood:	n/a
10	chr6:34524290-34524340	CMK	blood:	n/a
11	chr6:34524095-34524145	SKMC	muscle:	n/a
12	chr6:34543055-34543105	A549	lung:	n/a
13	chr6:34543055-34543105	HRPEpiC	eye:	n/a
14	chr6:34523925-34523975	NB4	blood:	n/a
15	chr6:34511514-34511564	SK-N-MC	brain:	n/a
16	chr6:34523925-34523975	HUVEC	blood vessel:	n/a
17	chr6:34514887-34514937	SK-N-MC	brain:	n/a
18	chr6:34512253-34512303	LNCaP	prostate:	n/a
19	chr6:34512253-34512303	RPTEC	kidney:	n/a
20	chr6:34524698-34524748	NHBE	bronchial:	n/a
21	chr6:34523925-34523975	Hela-S3	cervix:	n/a
22	chr6:34524097-34524147	HCPEpiC	choroid plexus:	n/a
23	chr6:34514887-34514937	Jurkat	blood:	n/a
24	chr6:34535602-34535652	HIPEpiC	eye:	n/a
25	chr6:34523925-34523975	NT2-D1	testis:	n/a
26	chr6:34511514-34511564	HEK293	kidney:	embryo
27	chr6:34524597-34524647	Jurkat	blood:	n/a
28	chr6:34525026-34525076	MCF10A-Er-Src	breast:	n/a
29	chr6:34528827-34528877	HNPCEpiC	eye:	n/a
30	chr6:34524097-34524147	HRE	kidney:	n/a
31	chr6:34524290-34524340	BE2_C	brain:	n/a
32	chr6:34524095-34524145	HepG2	liver:	n/a
33	chr6:34535602-34535652	Caco-2	colon:	n/a
34	chr6:34524766-34524816	HNPCEpiC	eye:	n/a
35	chr6:34524278-34524328	AG04449	skin:	fetal
36	chr6:34524766-34524816	HCM	heart:	n/a
37	chr6:34535602-34535652	PANC-1	pancreas:	n/a
38	chr6:34524278-34524328	BE2_C	brain:	n/a
39	chr6:34524278-34524328	AG09319	gingival:	n/a
40	chr6:34512253-34512303	HRE	kidney:	n/a
41	chr6:34524766-34524816	AG09319	gingival:	n/a
42	chr6:34514887-34514937	HNPCEpiC	eye:	n/a
43	chr6:34524278-34524328	HRCEpiC	kidney:	n/a
44	chr6:34524095-34524145	H1-hESC	embryonic stem cell:	embryo
45	chr6:34512215-34512265	MCF10A-Er-Src	breast:	n/a
46	chr6:34523925-34523975	ECC-1	luminal epithelium:	n/a
47	chr6:34524698-34524748	HEEpiC	esophagus:	n/a
48	chr6:34523925-34523975	HNPCEpiC	eye:	n/a
49	chr6:34524278-34524328	K562	blood:	n/a
50	chr6:34512253-34512303	HMEC	breast:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:34538087..34543232-chr6:34543693..34548004,8	K562	blood:
2	chr6:34205000..34207351-chr6:34521778..34524214,3	MCF-7	breast:
3	chr6:34527602..34533050-chr6:34533572..34539589,8	K562	blood:
4	chr6:34504144..34505003-chr6:34514225..34514901,2	MCF-7	breast:
5	chr6:34544544..34547164-chr6:34547916..34551672,4	K562	blood:
6	chr6:34494831..34497738-chr6:34508657..34510396,2	MCF-7	breast:
7	chr6:34543493..34547191-chr6:34549783..34553774,3	MCF-7	breast:
8	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
9	chr6:34532465..34535112-chr6:34540040..34542974,2	K562	blood:
10	chr6:34172530..34175474-chr6:34548744..34550732,2	K562	blood:
11	chr6:34548787..34550337-chr6:34551862..34554295,2	K562	blood:
12	chr6:34427383..34427978-chr6:34528004..34528902,2	MCF-7	breast:
13	chr6:34508361..34510823-chr6:34510978..34513076,2	MCF-7	breast:
14	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
15	chr6:34216270..34217861-chr6:34527614..34529829,2	MCF-7	breast:
16	chr6:34546025..34550946-chr6:34551862..34556143,7	K562	blood:
17	chr6:34514095..34516338-chr6:34543578..34545622,2	MCF-7	breast:
18	chr6:32936553..32938765-chr6:34521756..34523748,2	MCF-7	breast:
19	chr6:34505107..34506692-chr6:34515801..34518168,2	MCF-7	breast:
20	chr6:34544085..34546568-chr6:34548676..34550221,2	K562	blood:
21	chr6:34520436..34525113-chr6:34525166..34530447,6	K562	blood:
22	chr6:34491195..34497458-chr6:34528901..34533837,5	K562	blood:
23	chr6:34546025..34550946-chr6:34551862..34556143,7	K562	blood:
24	chr6:34435937..34438924-chr6:34520705..34523320,2	MCF-7	breast:
25	chr6:34532465..34535112-chr6:34540040..34542974,2	K562	blood:
26	chr6:34511760..34514306-chr6:34515453..34517552,2	K562	blood:
27	chr6:34501160..34503078-chr6:34510332..34511859,2	K562	blood:
28	chr6:34529337..34532289-chr6:34533729..34536883,4	K562	blood:
29	chr6:34529351..34531637-chr6:34540105..34542943,4	K562	blood:
30	chr6:34426702..34428652-chr6:34520960..34523550,2	MCF-7	breast:
31	chr6:34432385..34434700-chr6:34511007..34512543,2	MCF-7	breast:
32	chr6:34525385..34526922-chr6:34526989..34528671,2	K562	blood:
33	chr6:34518383..34520887-chr6:34564269..34566173,2	MCF-7	breast:
34	chr6:34507633..34511172-chr6:34512304..34515175,5	K562	blood:
35	chr6:34514887..34517520-chr6:34540730..34542846,2	MCF-7	breast:
36	chr6:34496932..34498060-chr6:34528153..34529212,4	MCF-7	breast:
37	chr6:34528981..34530580-chr6:34530582..34532257,2	MCF-7	breast:
38	chr6:34535538..34537048-chr6:34550660..34552218,2	K562	blood:
39	chr6:34205425..34208316-chr6:34542456..34544168,2	K562	blood:
40	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
41	chr6:34528906..34533005-chr6:34533870..34536568,4	MCF-7	breast:
42	chr6:34550788..34556388-chr6:34565460..34570894,5	K562	blood:
43	chr6:34506980..34511719-chr6:34518115..34520438,4	K562	blood:
44	chr18:50300436..50303454-chr6:34521553..34523812,3	MCF-7	breast:
45	chr6:34496034..34498791-chr6:34510835..34512433,2	K562	blood:
46	chr6:34551284..34553223-chr6:34555958..34557670,2	MCF-7	breast:
47	chr6:34265209..34267014-chr6:34530646..34533613,2	K562	blood:
48	chr6:34528717..34530463-chr6:34574776..34577421,2	K562	blood:
49	chr6:34514003..34515621-chr6:34528599..34531450,2	K562	blood:
50	chr6:34527129..34529225-chr6:34531595..34533511,2	K562	blood:

No data

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

Extended variants
information (count: 1919 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1919 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560465376	chr6:34509817-34509818	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs564611116	chr6:34509828-34509829	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs530584002	chr6:34509837-34509838	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs190493199	chr6:34509885-34509886	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs549150418	chr6:34509894-34509895	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs567488533	chr6:34509901-34509902	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs529351945	chr6:34509936-34509937	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs550779113	chr6:34509940-34509941	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs372729689	chr6:34509947-34509948	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs377295100	chr6:34509972-34509973	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs55899330	chr6:34509977-34509978	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs143290528	chr6:34509999-34510000	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs558171938	chr6:34510063-34510064	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs76926240	chr6:34510066-34510067	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559341403	chr6:34510084-34510085	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs555513983	chr6:34510092-34510093	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs371935239	chr6:34510096-34510097	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs180907360	chr6:34510137-34510138	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528134896	chr6:34510141-34510142	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544825531	chr6:34510190-34510191	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs555967724	chr6:34510220-34510221	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7761030	chr6:34510223-34510224	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs544672082	chr6:34510232-34510233	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs148336383	chr6:34510233-34510234	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188273116	chr6:34510283-34510284	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs141461964	chr6:34510287-34510288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181384731	chr6:34510304-34510305	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs146313774	chr6:34510321-34510322	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs138196128	chr6:34510342-34510343	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs143084951	chr6:34510344-34510345	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs533476078	chr6:34510359-34510360	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs79651747	chr6:34510376-34510377	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs369090518	chr6:34510383-34510384	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs550784539	chr6:34510414-34510415	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534189218	chr6:34510441-34510442	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs549250709	chr6:34510487-34510488	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs567980810	chr6:34510494-34510495	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs538054464	chr6:34510495-34510496	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs146143364	chr6:34510522-34510523	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs562280021	chr6:34510532-34510533	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs570634011	chr6:34510543-34510544	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs9348947	chr6:34510557-34510558	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs577626203	chr6:34510592-34510593	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs186425948	chr6:34510635-34510636	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs553766457	chr6:34510698-34510699	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572053051	chr6:34510702-34510703	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs542669750	chr6:34510707-34510708	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs561162974	chr6:34510708-34510709	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs576326500	chr6:34510712-34510713	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs543210890	chr6:34510733-34510734	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34498200-34514200	Weak transcription	Right Ventricle	heart
2	chr6:34500600-34513800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr6:34505000-34513200	Weak transcription	Fetal Intestine Small	intestine
4	chr6:34505200-34512600	Weak transcription	Fetal Brain Male	brain
5	chr6:34505400-34512600	Weak transcription	Stomach Mucosa	stomach
6	chr6:34505400-34514200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr6:34505600-34511000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:34505600-34511000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr6:34505800-34510200	Strong transcription	Fetal Stomach	stomach
10	chr6:34505800-34513200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:34506000-34510000	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr6:34506000-34511200	Weak transcription	A549	lung
13	chr6:34506200-34512400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr6:34506200-34512800	Weak transcription	Colonic Mucosa	Colon
15	chr6:34506400-34513800	Weak transcription	Gastric	stomach
16	chr6:34507400-34511400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:34507600-34512600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:34509800-34510000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:34510000-34510200	Enhancers	Spleen	Spleen
20	chr6:34510000-34510400	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr6:34510200-34511400	Weak transcription	Spleen	Spleen
22	chr6:34510200-34514000	Weak transcription	Fetal Stomach	stomach
23	chr6:34510400-34512600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr6:34511000-34511200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr6:34511000-34512000	Enhancers	HSMM	muscle
26	chr6:34511000-34512000	Enhancers	HUVEC	blood vessel
27	chr6:34511000-34512200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr6:34511000-34512600	Enhancers	NH-A	brain
29	chr6:34511000-34512600	Enhancers	Osteobl	bone
30	chr6:34511000-34512800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr6:34511000-34512800	Enhancers	Hela-S3	cervix
32	chr6:34511000-34513000	Enhancers	HSMMtube	muscle
33	chr6:34511200-34511600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr6:34511200-34511800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr6:34511200-34511800	Bivalent Enhancer	HepG2	liver
36	chr6:34511200-34512400	Enhancers	K562	blood
37	chr6:34511200-34512600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr6:34511200-34512600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr6:34511200-34512800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:34511200-34513800	Enhancers	A549	lung
41	chr6:34511400-34511600	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr6:34511400-34511800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:34511400-34511800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr6:34511400-34512000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr6:34511400-34512000	Enhancers	Spleen	Spleen
46	chr6:34511400-34515200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:34511600-34511800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:34511800-34512000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr6:34511800-34512200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr6:34511800-34514000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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