Variant report

Variant	esv3475167
Chromosome Location	chr6:150003006-150086225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2690)
CpG islands
(count:2563)
Chromatin interactive
region (count:159)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2690 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150039257-150039878	K562	blood:	n/a	n/a
2	ARID3A	chr6:150017933-150018010	K562	blood:	n/a	n/a
3	ARID3A	chr6:150038569-150038782	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:150030569-150030771	K562	blood:	n/a	n/a
5	ARID3A	chr6:150066932-150068089	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:150044980-150045580	K562	blood:	n/a	n/a
7	ARID3A	chr6:150081008-150081179	K562	blood:	n/a	n/a
8	ARID3A	chr6:150044982-150045511	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:150032882-150033189	K562	blood:	n/a	n/a
10	ARID3A	chr6:150082129-150082787	K562	blood:	n/a	n/a
11	ARID3A	chr6:150039096-150039926	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:150048503-150050072	K562	blood:	n/a	n/a
13	ARID3A	chr6:150070595-150072105	HepG2	liver:	n/a	n/a
14	ATF1	chr6:150049312-150050037	K562	blood:	n/a	n/a
15	ATF1	chr6:150030368-150030520	K562	blood:	n/a	n/a
16	ATF1	chr6:150044999-150045306	K562	blood:	n/a	n/a
17	ATF1	chr6:150039597-150039955	K562	blood:	n/a	n/a
18	ATF1	chr6:150032958-150033251	K562	blood:	n/a	n/a
19	ATF1	chr6:150082630-150082823	K562	blood:	n/a	n/a
20	ATF1	chr6:150075740-150076027	K562	blood:	n/a	n/a
21	ATF2	chr6:150007761-150008300	GM12878	blood:	n/a	n/a
22	ATF2	chr6:150038666-150039293	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr6:150076427-150076824	GM12878	blood:	n/a	n/a
24	ATF2	chr6:150039083-150039878	GM12878	blood:	n/a	n/a
25	ATF2	chr6:150067293-150068229	GM12878	blood:	n/a	n/a
26	ATF2	chr6:150070578-150071106	GM12878	blood:	n/a	n/a
27	ATF2	chr6:150039268-150039675	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:150071127-150071551	GM12878	blood:	n/a	n/a
29	ATF2	chr6:150038706-150039577	GM12878	blood:	n/a	n/a
30	ATF2	chr6:150067401-150067869	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr6:150082497-150083008	GM12878	blood:	n/a	n/a
32	ATF2	chr6:150067400-150067880	GM12878	blood:	n/a	n/a
33	ATF2	chr6:150082478-150083101	GM12878	blood:	n/a	n/a
34	ATF2	chr6:150076385-150076875	GM12878	blood:	n/a	n/a
35	ATF3	chr6:150070587-150071123	K562	blood:	n/a	n/a
36	ATF3	chr6:150044888-150045348	K562	blood:	n/a	n/a
37	ATF3	chr6:150070533-150071018	K562	blood:	n/a	n/a
38	BACH1	chr6:150038522-150039545	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr6:150032900-150032965	K562	blood:	n/a	n/a
40	BACH1	chr6:150070692-150071606	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr6:150067616-150067884	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr6:150070534-150070753	GM12878	blood:	n/a	chr6:150070716-150070727
43	BATF	chr6:150037341-150037644	GM12878	blood:	n/a	n/a
44	BATF	chr6:150007815-150008198	GM12878	blood:	n/a	n/a
45	BATF	chr6:150037325-150037646	GM12878	blood:	n/a	n/a
46	BATF	chr6:150007877-150008165	GM12878	blood:	n/a	n/a
47	BATF	chr6:150070518-150070852	GM12878	blood:	n/a	chr6:150070716-150070727
48	BCL11A	chr6:150076425-150076763	GM12878	blood:	n/a	n/a
49	BCL11A	chr6:150076507-150076746	GM12878	blood:	n/a	n/a
50	BCL3	chr6:150038895-150039538	GM12878	blood:	n/a	n/a

(count:2563 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150042818-150042868	CMK	blood:	n/a
2	chr6:150042818-150042868	CMK	blood:	n/a
3	chr6:150039767-150039817	AoSMC	blood vessel:	n/a
4	chr6:150038700-150038750	BJ	skin:	n/a
5	chr6:150070727-150070777	Hepatocyte	liver:	n/a
6	chr6:150071161-150071211	AG10803	skin:	n/a
7	chr6:150070697-150070747	AoSMC	blood vessel:	n/a
8	chr6:150070697-150070747	SAEC	small airway:	n/a
9	chr6:150039330-150039380	HepG2	liver:	n/a
10	chr6:150070202-150070252	T-47D	breast:	n/a
11	chr6:150039699-150039749	HepG2	liver:	n/a
12	chr6:150070705-150070755	H1-hESC	embryonic stem cell:	embryo
13	chr6:150071069-150071119	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:150039190-150039240	PrEC	prostate:	n/a
15	chr6:150039330-150039380	GM12878	blood:	n/a
16	chr6:150067491-150067541	ECC-1	luminal epithelium:	n/a
17	chr6:150067846-150067896	SAEC	small airway:	n/a
18	chr6:150039435-150039485	LNCaP	prostate:	n/a
19	chr6:150038700-150038750	A549	lung:	n/a
20	chr6:150039536-150039586	HepG2	liver:	n/a
21	chr6:150035399-150035449	HCT-116	colon:	n/a
22	chr6:150039439-150039489	NT2-D1	testis:	n/a
23	chr6:150045504-150045554	HepG2	liver:	n/a
24	chr6:150070787-150070837	HUVEC	blood vessel:	n/a
25	chr6:150068017-150068067	SK-N-SH_RA	brain:	n/a
26	chr6:150068017-150068067	HNPCEpiC	eye:	n/a
27	chr6:150038536-150038586	ProgFib	skin:	n/a
28	chr6:150067640-150067690	NB4	blood:	n/a
29	chr6:150035399-150035449	BJ	skin:	n/a
30	chr6:150042818-150042868	HCM	heart:	n/a
31	chr6:150067644-150067694	SAEC	small airway:	n/a
32	chr6:150038956-150039006	HRPEpiC	eye:	n/a
33	chr6:150070705-150070755	GM12878	blood:	n/a
34	chr6:150067738-150067788	HL-60	blood:	n/a
35	chr6:150029611-150029661	IMR90	lung:	fetal
36	chr6:150039400-150039450	GM06990	blood:	n/a
37	chr6:150068017-150068067	BE2_C	brain:	n/a
38	chr6:150073879-150073929	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:150039666-150039716	NHDF-neo	bronchial:	n/a
40	chr6:150070727-150070777	T-47D	breast:	n/a
41	chr6:150067846-150067896	HEEpiC	esophagus:	n/a
42	chr6:150070727-150070777	HCF	heart:	n/a
43	chr6:150070997-150071047	MCF-7	breast:	n/a
44	chr6:150039439-150039489	SAEC	small airway:	n/a
45	chr6:150039767-150039817	PrEC	prostate:	n/a
46	chr6:150068006-150068056	Hepatocyte	liver:	n/a
47	chr6:150070697-150070747	HCPEpiC	choroid plexus:	n/a
48	chr6:150067466-150067516	ECC-1	luminal epithelium:	n/a
49	chr6:150073879-150073929	AG09319	gingival:	n/a
50	chr6:150070202-150070252	NH-A	brain:	n/a

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:149981488..149983394-chr6:150012871..150015701,2	K562	blood:
2	chr6:150012116..150014440-chr6:150030723..150032247,2	K562	blood:
3	chr6:150067696..150070482-chr6:150117638..150119336,2	K562	blood:
4	chr6:150014915..150016928-chr6:150021658..150023667,2	K562	blood:
5	chr6:150080552..150082933-chr6:150085162..150087881,2	K562	blood:
6	chr6:150037459..150041467-chr6:150046998..150054266,14	K562	blood:
7	chr6:150071379..150074045-chr6:150185232..150187132,2	MCF-7	breast:
8	chr6:149996900..150000270-chr6:150001937..150004425,4	K562	blood:
9	chr6:150037915..150040218-chr6:150069685..150072655,4	MCF-7	breast:
10	chr6:150022443..150028756-chr6:150036776..150040441,8	MCF-7	breast:
11	chr1:145506973..145507728-chr6:150070463..150070969,2	NB4	blood:
12	chr6:150045603..150048422-chr6:150052739..150054245,2	MCF-7	breast:
13	chr6:150068048..150069727-chr6:150083156..150084821,2	MCF-7	breast:
14	chr6:149967309..149971944-chr6:150037502..150040952,6	MCF-7	breast:
15	chr6:150045566..150048616-chr6:150051147..150053012,3	K562	blood:
16	chr6:150049432..150051303-chr6:150051531..150054391,2	K562	blood:
17	chr6:150045251..150047149-chr6:150058484..150059997,2	K562	blood:
18	chr6:150038744..150042586-chr6:150067819..150072874,7	K562	blood:
19	chr6:150013652..150017218-chr6:150037268..150040807,4	MCF-7	breast:
20	chr6:150036817..150045008-chr6:150066563..150073628,17	MCF-7	breast:
21	chr6:150013102..150015121-chr6:150171390..150174211,2	K562	blood:
22	chr6:150061815..150065495-chr6:150065702..150069164,4	MCF-7	breast:
23	chr6:149887426..149891060-chr6:150037726..150040656,4	K562	blood:
24	chr6:150080535..150082998-chr6:150090034..150092678,2	MCF-7	breast:
25	chr6:150043756..150046573-chr6:150046900..150049362,3	K562	blood:
26	chr6:150004823..150006721-chr6:150008544..150010327,2	K562	blood:
27	chr6:150067902..150070845-chr6:150079961..150081547,2	K562	blood:
28	chr6:150075319..150077363-chr6:150091174..150093691,2	MCF-7	breast:
29	chr6:150005972..150008566-chr6:150038715..150040763,2	K562	blood:
30	chr6:149968177..149971048-chr6:150069429..150073118,6	K562	blood:
31	chr6:150045251..150047149-chr6:150058484..150059997,2	K562	blood:
32	chr6:149865412..149868638-chr6:150066732..150070347,4	K562	blood:
33	chr6:150048960..150051066-chr6:150070232..150072342,2	K562	blood:
34	chr6:150067770..150069561-chr6:150184088..150185718,2	MCF-7	breast:
35	chr6:150085048..150087027-chr6:150091947..150093777,2	MCF-7	breast:
36	chr6:149968511..149970229-chr6:150002513..150004622,2	K562	blood:
37	chr6:149864465..149868641-chr6:150037478..150040253,6	MCF-7	breast:
38	chr6:150072577..150074857-chr6:150088805..150091239,2	K562	blood:
39	chr6:150050583..150052952-chr6:150059136..150060763,2	K562	blood:
40	chr6:150005221..150006846-chr6:150008544..150010476,2	K562	blood:
41	chr6:150041722..150043504-chr6:150190931..150192502,2	MCF-7	breast:
42	chr6:150038868..150039820-chr6:150070353..150070958,2	MCF-7	breast:
43	chr6:111195402..111196360-chr6:150039114..150039744,2	Hela-S3	cervix:
44	chr6:149969487..149971965-chr6:150038903..150040820,3	K562	blood:
45	chr6:150063981..150065532-chr6:150069623..150071188,2	K562	blood:
46	chr6:149968317..149970120-chr6:150005656..150008521,2	K562	blood:
47	chr6:150068048..150069727-chr6:150083156..150084821,2	MCF-7	breast:
48	chr6:150037654..150039450-chr6:150083090..150085436,2	K562	blood:
49	chr6:149884840..149889202-chr6:150038504..150040931,4	K562	blood:
50	chr6:149966676..149970226-chr6:150037413..150039390,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LATS1-1	chr6:150022313-150023656	expReg_chr6_11218_-

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	NUP43	hsa-miR-32-5p	chr6:150047119-150047112
2	NUP43	hsa-miR-32-5p	chr6:150047113-150047134
3	NUP43	hsa-miR-32-5p	chr6:150048035-150048052

Variant related genes	Relation type
PCMT1	TF binding region
LATS1	TF binding region
NUP43	TF binding region
PCMT1	CpG island
LATS1	CpG island
NUP43	CpG island
ENSG00000235168	chromatin interactions
ENSG00000055044	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000120253	chromatin interactions
ENSG00000123505	chromatin interactions
ENSG00000131795	chromatin interactions
ENSG00000248008	chromatin interactions
ENSG00000236591	chromatin interactions
ENSG00000120265	chromatin interactions
ENSG00000197061	chromatin interactions
ENSG00000160783	chromatin interactions
ENSG00000234222	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000273132	chromatin interactions
ENSG00000268592	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000131023	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000186625	chromatin interactions
ENSG00000260238	chromatin interactions
ENSG00000131013	chromatin interactions
ENSG00000146826	chromatin interactions
ENSG00000088986	chromatin interactions
ENSG00000055211	chromatin interactions
ENSG00000231760	chromatin interactions

Extended variants
information (count: 3282 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3282 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573861538	chr6:150003020-150003021	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs564129932	chr6:150003053-150003054	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542980219	chr6:150003075-150003076	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78553600	chr6:150003078-150003079	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530970914	chr6:150003108-150003109	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs9505990	chr6:150003111-150003112	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs11758633	chr6:150003169-150003170	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564611459	chr6:150003172-150003173	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533232550	chr6:150003173-150003174	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs147884962	chr6:150003180-150003181	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148925752	chr6:150003203-150003204	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs71925661	chr6:150003227-150003228	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200077120	chr6:150003228-150003229	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567051239	chr6:150003241-150003242	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371480554	chr6:150003246-150003247	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11462051	chr6:150003256-150003257	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs535636311	chr6:150003257-150003258	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs61386393	chr6:150003261-150003262	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs529555809	chr6:150003282-150003283	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142761926	chr6:150003320-150003321	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs569163332	chr6:150003329-150003330	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs151016464	chr6:150003418-150003419	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537458273	chr6:150003431-150003432	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549611060	chr6:150003452-150003453	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs78456599	chr6:150003515-150003516	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs183609383	chr6:150003537-150003538	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375761267	chr6:150003538-150003539	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553817152	chr6:150003555-150003556	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573924160	chr6:150003572-150003573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs111568839	chr6:150003608-150003609	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372442507	chr6:150003609-150003610	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538364850	chr6:150003616-150003617	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576361057	chr6:150003617-150003618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544607335	chr6:150003622-150003623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs186890890	chr6:150003648-150003649	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533338171	chr6:150003649-150003650	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs527967501	chr6:150003714-150003715	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540404561	chr6:150003738-150003739	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs560203066	chr6:150003780-150003781	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575525509	chr6:150003825-150003826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138662732	chr6:150003829-150003830	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs114964673	chr6:150003832-150003833	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557939156	chr6:150003842-150003843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569226129	chr6:150003860-150003861	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531856612	chr6:150003863-150003864	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116649008	chr6:150003895-150003896	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs571192638	chr6:150003896-150003897	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs115958197	chr6:150003926-150003927	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs9505991	chr6:150003943-150003944	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553636029	chr6:150004005-150004006	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4148 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149977200-150022600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:149977800-150005800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:149977800-150020600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:149978000-150029200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:149980000-150003400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr6:149980000-150008000	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr6:149980600-150024800	Strong transcription	Fetal Thymus	thymus
8	chr6:149980800-150005800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:149981200-150018800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr6:149982400-150004400	Weak transcription	Right Atrium	heart
11	chr6:149982800-150003400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:149983400-150004200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr6:149983800-150004400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:149983800-150005800	Strong transcription	Fetal Muscle Trunk	muscle
15	chr6:149984600-150004400	Weak transcription	A549	lung
16	chr6:149987000-150036800	Weak transcription	Hela-S3	cervix
17	chr6:149988200-150008000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:149990400-150003600	Weak transcription	Pancreas	Pancrea
19	chr6:149990400-150004200	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr6:149990600-150004400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:149991000-150004600	Weak transcription	Aorta	Aorta
22	chr6:149992000-150004200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr6:149994600-150012600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:149995800-150004400	Weak transcription	Stomach Mucosa	stomach
25	chr6:149996800-150004400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr6:149997200-150004400	Weak transcription	Psoas Muscle	Psoas
27	chr6:149997400-150003200	Weak transcription	Brain Hippocampus Middle	brain
28	chr6:149997800-150004200	Weak transcription	Rectal Smooth Muscle	rectum
29	chr6:149997800-150004400	Weak transcription	Brain Germinal Matrix	brain
30	chr6:149997800-150004400	Weak transcription	Esophagus	oesophagus
31	chr6:149997800-150004400	Weak transcription	Ovary	ovary
32	chr6:149997800-150004400	Weak transcription	Right Ventricle	heart
33	chr6:149997800-150004400	Weak transcription	Spleen	Spleen
34	chr6:149997800-150027400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr6:149998000-150003400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:149998000-150003600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:149998000-150004200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr6:149998000-150004200	Weak transcription	Fetal Brain Female	brain
39	chr6:149998000-150004200	Weak transcription	HUVEC	blood vessel
40	chr6:149998000-150004400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr6:149998000-150004400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr6:149998000-150004400	Weak transcription	Brain Anterior Caudate	brain
43	chr6:149998000-150004400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr6:149998000-150004400	Weak transcription	Gastric	stomach
45	chr6:149998000-150004400	Weak transcription	Left Ventricle	heart
46	chr6:149998000-150004400	Weak transcription	Lung	lung
47	chr6:149998000-150004800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:149998000-150020800	Weak transcription	Small Intestine	intestine
49	chr6:149998000-150029800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr6:149998200-150004400	Weak transcription	H9 Cell Line	embryonic stem cell

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