Variant report

Variant	nsv885912
Chromosome Location	chr6:56327849-56458836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2040)
CpG islands
(count:915)
Chromatin interactive
region (count:99)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2040 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:56386126-56386671	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:56375694-56376414	K562	blood:	n/a	n/a
3	ARID3A	chr6:56407528-56407947	K562	blood:	n/a	n/a
4	ARID3A	chr6:56375672-56376421	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:56405792-56406934	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:56407505-56408262	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:56457752-56457946	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:56347324-56347724	HepG2	liver:	n/a	chr6:56347701-56347717
9	ARID3A	chr6:56393076-56393137	K562	blood:	n/a	n/a
10	ARID3A	chr6:56436486-56436727	HepG2	liver:	n/a	n/a
11	ATF1	chr6:56375892-56376849	K562	blood:	n/a	n/a
12	ATF1	chr6:56407166-56408203	K562	blood:	n/a	n/a
13	ATF1	chr6:56356642-56357113	K562	blood:	n/a	n/a
14	ATF1	chr6:56406049-56406522	K562	blood:	n/a	n/a
15	ATF1	chr6:56387112-56387441	K562	blood:	n/a	n/a
16	ATF2	chr6:56407196-56408142	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr6:56407255-56408020	GM12878	blood:	n/a	n/a
18	ATF2	chr6:56407171-56408263	GM12878	blood:	n/a	n/a
19	ATF2	chr6:56407373-56408031	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr6:56458359-56459077	GM12878	blood:	n/a	n/a
21	ATF2	chr6:56458334-56459197	GM12878	blood:	n/a	n/a
22	ATF3	chr6:56407572-56407934	K562	blood:	n/a	chr6:56407777-56407790 chr6:56407778-56407791
23	ATF3	chr6:56407635-56407886	K562	blood:	n/a	chr6:56407777-56407790 chr6:56407778-56407791
24	BACH1	chr6:56407432-56407766	K562	blood:	n/a	n/a
25	BACH1	chr6:56358399-56358500	K562	blood:	n/a	n/a
26	BACH1	chr6:56407596-56408105	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:56417752-56417775	K562	blood:	n/a	n/a
28	BATF	chr6:56458498-56459037	GM12878	blood:	n/a	n/a
29	BATF	chr6:56407495-56407907	GM12878	blood:	n/a	chr6:56407777-56407790
30	BATF	chr6:56458441-56459089	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:56458501-56458955	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:56398008-56398320	GM12878	blood:	n/a	n/a
33	BCL11A	chr6:56458422-56459075	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:56407246-56408209	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:56458306-56459214	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:56407145-56407997	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:56435557-56435948	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:56376020-56376425	K562	blood:	n/a	n/a
39	BHLHE40	chr6:56458519-56459096	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:56341007-56341129	K562	blood:	n/a	n/a
41	BHLHE40	chr6:56435567-56435913	GM12878	blood:	n/a	n/a
42	BHLHE40	chr6:56347336-56347665	HepG2	liver:	n/a	n/a
43	BHLHE40	chr6:56407280-56408103	K562	blood:	n/a	n/a
44	BHLHE40	chr6:56407271-56408106	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:56407388-56408057	HepG2	liver:	n/a	n/a
46	BHLHE40	chr6:56435578-56436071	K562	blood:	n/a	n/a
47	BHLHE40	chr6:56361133-56361251	K562	blood:	n/a	n/a
48	BRCA1	chr6:56407132-56408012	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr6:56407506-56407713	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr6:56407311-56407961	HepG2	liver:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:56407725-56407775	NB4	blood:	n/a
2	chr6:56405167-56405217	PrEC	prostate:	n/a
3	chr6:56371192-56371242	GM06990	blood:	n/a
4	chr6:56389866-56389916	AG09309	skin:	n/a
5	chr6:56389866-56389916	LNCaP	prostate:	n/a
6	chr6:56414724-56414774	HL-60	blood:	n/a
7	chr6:56357077-56357127	NT2-D1	testis:	n/a
8	chr6:56438637-56438687	T-47D	breast:	n/a
9	chr6:56357077-56357127	RPTEC	kidney:	n/a
10	chr6:56407956-56408006	AG04449	skin:	fetal
11	chr6:56405167-56405217	GM12878	blood:	n/a
12	chr6:56407956-56408006	HMEC	breast:	n/a
13	chr6:56407538-56407588	Hepatocyte	liver:	n/a
14	chr6:56406336-56406386	BJ	skin:	n/a
15	chr6:56371192-56371242	ovcar-3	ovarian:	n/a
16	chr6:56400181-56400231	HCF	heart:	n/a
17	chr6:56406336-56406386	NB4	blood:	n/a
18	chr6:56391215-56391265	AG04450	lung:	fetal
19	chr6:56391215-56391265	HCPEpiC	choroid plexus:	n/a
20	chr6:56407925-56407975	AG09319	gingival:	n/a
21	chr6:56406336-56406386	H1-hESC	embryonic stem cell:	embryo
22	chr6:56371192-56371242	AG09309	skin:	n/a
23	chr6:56407956-56408006	SKMC	muscle:	n/a
24	chr6:56371192-56371242	AG09319	gingival:	n/a
25	chr6:56389866-56389916	PFSK-1	brain:	n/a
26	chr6:56405167-56405217	ProgFib	skin:	n/a
27	chr6:56387378-56387428	HepG2	liver:	n/a
28	chr6:56400181-56400231	HRE	kidney:	n/a
29	chr6:56414724-56414774	Hepatocyte	liver:	n/a
30	chr6:56405167-56405217	SK-N-MC	brain:	n/a
31	chr6:56407725-56407775	SK-N-MC	brain:	n/a
32	chr6:56406084-56406134	NHDF-neo	bronchial:	n/a
33	chr6:56391215-56391265	AG09319	gingival:	n/a
34	chr6:56389866-56389916	GM12891	blood:	n/a
35	chr6:56406336-56406386	SK-N-SH	brain:	n/a
36	chr6:56400181-56400231	NT2-D1	testis:	n/a
37	chr6:56406084-56406134	K562	blood:	n/a
38	chr6:56387378-56387428	BJ	skin:	n/a
39	chr6:56407956-56408006	AoSMC	blood vessel:	n/a
40	chr6:56371192-56371242	Jurkat	blood:	n/a
41	chr6:56357077-56357127	HMEC	breast:	n/a
42	chr6:56400181-56400231	HIPEpiC	eye:	n/a
43	chr6:56405167-56405217	ovcar-3	ovarian:	n/a
44	chr6:56400181-56400231	T-47D	breast:	n/a
45	chr6:56438637-56438687	HEEpiC	esophagus:	n/a
46	chr6:56407956-56408006	NH-A	brain:	n/a
47	chr6:56389866-56389916	HRCEpiC	kidney:	n/a
48	chr6:56389866-56389916	HUVEC	blood vessel:	n/a
49	chr6:56371192-56371242	BE2_C	brain:	n/a
50	chr6:56371192-56371242	HRCEpiC	kidney:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:56234903..56235822-chr6:56379977..56380797,2	MCF-7	breast:
2	chr6:56347192..56349659-chr6:56354834..56357986,4	K562	blood:
3	chr6:56340912..56343256-chr6:56347717..56349911,2	MCF-7	breast:
4	chr6:56379723..56396922-chr6:56400495..56411638,31	K562	blood:
5	chr6:56223761..56224766-chr6:56435256..56436214,5	K562	blood:
6	chr6:56234558..56235401-chr6:56435496..56436175,3	MCF-7	breast:
7	chr6:56228029..56228715-chr6:56457678..56458269,2	MCF-7	breast:
8	chr6:56330615..56332340-chr6:56407927..56409613,2	K562	blood:
9	chr6:56409064..56410806-chr6:56424133..56426193,2	K562	blood:
10	chr6:56410167..56412439-chr6:56412999..56414699,2	K562	blood:
11	chr6:56390066..56391904-chr6:56396984..56399522,2	MCF-7	breast:
12	chr6:56383107..56384935-chr6:56387446..56390248,2	K562	blood:
13	chr6:56336959..56338872-chr6:56404795..56407459,2	K562	blood:
14	chr6:56413498..56416394-chr6:56417084..56419483,2	K562	blood:
15	chr6:56383088..56384699-chr6:56407591..56409338,2	K562	blood:
16	chr6:56223731..56224682-chr6:56457326..56458340,3	MCF-7	breast:
17	chr6:56383107..56384935-chr6:56387446..56390248,2	K562	blood:
18	chr6:56363593..56367188-chr6:56368013..56370218,3	MCF-7	breast:
19	chr6:56335330..56337721-chr6:56339949..56341801,2	K562	blood:
20	chr6:56403956..56410167-chr6:56410483..56413824,9	K562	blood:
21	chr6:56398077..56400962-chr6:56401619..56403800,2	K562	blood:
22	chr6:56392217..56393976-chr6:56395740..56397459,2	K562	blood:
23	chr6:56302630..56305077-chr6:56407760..56410392,2	MCF-7	breast:
24	chr6:56347192..56349659-chr6:56354834..56357164,3	K562	blood:
25	chr6:56374485..56377341-chr6:56380470..56384676,4	MCF-7	breast:
26	chr6:56333512..56335429-chr6:56408876..56410830,2	K562	blood:
27	chr6:56374485..56377341-chr6:56380470..56384676,4	MCF-7	breast:
28	chr6:56385896..56387722-chr6:56406237..56408892,2	MCF-7	breast:
29	chr6:56406220..56410337-chr6:56413126..56418049,5	MCF-7	breast:
30	chr6:56376106..56377836-chr6:56404859..56408896,4	K562	blood:
31	chr6:56347192..56349659-chr6:56354834..56357164,3	K562	blood:
32	chr6:56407223..56407766-chr9:2014757..2015410,2	NB4	blood:
33	chr6:56359297..56362081-chr6:56378593..56380440,2	K562	blood:
34	chr6:56416932..56418493-chr6:56421401..56422998,2	MCF-7	breast:
35	chr6:56362725..56365186-chr6:56367479..56371107,3	K562	blood:
36	chr6:56376171..56378986-chr6:56407329..56410206,2	K562	blood:
37	chr6:56371302..56373415-chr6:56374644..56377108,2	K562	blood:
38	chr6:56405751..56407545-chr6:56409347..56411136,2	MCF-7	breast:
39	chr6:56370282..56372107-chr6:56378887..56380737,2	K562	blood:
40	chr6:56223580..56224741-chr6:56457433..56458422,8	K562	blood:
41	chr1:222517973..222518488-chr6:56394311..56395250,2	MCF-7	breast:
42	chr6:56234525..56235479-chr6:56413389..56414430,8	MCF-7	breast:
43	chr6:56370809..56373672-chr6:56406275..56408971,3	K562	blood:
44	chr6:56350906..56352815-chr6:56354860..56356962,2	K562	blood:
45	chr6:56386785..56388815-chr6:56390586..56392837,2	MCF-7	breast:
46	chr6:56406262..56407921-chr6:56416925..56419390,3	K562	blood:
47	chr6:56392217..56393976-chr6:56395740..56397459,2	K562	blood:
48	chr6:56234937..56235452-chr6:56457486..56458082,2	MCF-7	breast:
49	chr6:56179482..56180209-chr6:56435647..56436284,2	MCF-7	breast:
50	chr6:56326705..56328808-chr6:56330727..56334737,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL21A1-2	chr6:56330876-56330911	NONHSAT113244
2	lnc-COL21A1-2	chr6:56329149-56329554	NONHSAT113244

No data

Variant related genes	Relation type
DST	TF binding region
DST	CpG island
ENSG00000102897	chromatin interactions
ENSG00000080503	chromatin interactions
ENSG00000151914	chromatin interactions
ENSG00000215301	chromatin interactions
ENSG00000196678	chromatin interactions
ENSG00000188215	chromatin interactions

Extended variants
information (count: 4775 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4775 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11758339	chr6:56327849-56327850	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144012429	chr6:56327856-56327857	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201991278	chr6:56327859-56327860	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs373660690	chr6:56327872-56327873	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs201138592	chr6:56327879-56327880	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs371560478	chr6:56327926-56327927	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375019954	chr6:56327950-56327951	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs546355407	chr6:56327951-56327952	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551923109	chr6:56327979-56327980	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs143954921	chr6:56327996-56327997	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559832803	chr6:56327997-56327998	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs146419099	chr6:56328065-56328066	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187433214	chr6:56328110-56328111	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560531687	chr6:56328117-56328118	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192935625	chr6:56328127-56328128	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563509627	chr6:56328173-56328174	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs114556571	chr6:56328205-56328206	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567980821	chr6:56328290-56328291	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144883191	chr6:56328291-56328292	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550178084	chr6:56328311-56328312	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs184618654	chr6:56328317-56328318	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539150671	chr6:56328331-56328332	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371934678	chr6:56328333-56328334	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375303601	chr6:56328360-56328361	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs557488147	chr6:56328368-56328369	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs201293893	chr6:56328377-56328378	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201952309	chr6:56328383-56328384	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs202108973	chr6:56328384-56328385	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs374094129	chr6:56328390-56328391	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs554371778	chr6:56328399-56328400	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs567935553	chr6:56328405-56328406	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs201429821	chr6:56328406-56328407	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs200298542	chr6:56328416-56328417	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200781365	chr6:56328426-56328427	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201785384	chr6:56328451-56328452	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377586570	chr6:56328462-56328463	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs370820734	chr6:56328465-56328466	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375687689	chr6:56328517-56328518	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs377398339	chr6:56328593-56328594	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs138743151	chr6:56328624-56328625	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs116618656	chr6:56328663-56328664	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs556883444	chr6:56328666-56328667	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs368302586	chr6:56328708-56328709	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs55903203	chr6:56328712-56328713	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs188758419	chr6:56328740-56328741	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs73747832	chr6:56328769-56328770	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs368711729	chr6:56328770-56328771	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs543240027	chr6:56328890-56328891	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs545740461	chr6:56328901-56328902	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76078908	chr6:56328926-56328927	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	22522925	CNVD
Central neurocytomas	17123091	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:4822 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56308800-56373800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:56315000-56347200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:56315000-56349800	Strong transcription	HSMM	muscle
4	chr6:56315600-56371000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:56315800-56329200	Weak transcription	Small Intestine	intestine
6	chr6:56316800-56337600	Weak transcription	Hela-S3	cervix
7	chr6:56317200-56342800	Strong transcription	Muscle Satellite Cultured Cells	--
8	chr6:56317800-56331200	Strong transcription	HSMMtube	muscle
9	chr6:56318000-56340600	Strong transcription	Fetal Intestine Large	intestine
10	chr6:56318600-56331000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:56318800-56332000	Strong transcription	Fetal Lung	lung
12	chr6:56319000-56331200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:56319000-56348200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:56319200-56331200	Strong transcription	Osteobl	bone
15	chr6:56319200-56340400	Strong transcription	NH-A	brain
16	chr6:56319200-56348400	Strong transcription	NHDF-Ad	bronchial
17	chr6:56319400-56329200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:56319400-56343600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:56319400-56344200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:56320000-56338800	Strong transcription	Liver	Liver
21	chr6:56320800-56328600	Strong transcription	Brain Substantia Nigra	brain
22	chr6:56320800-56331200	Strong transcription	Brain Anterior Caudate	brain
23	chr6:56321000-56331000	Strong transcription	Stomach Smooth Muscle	stomach
24	chr6:56321000-56331200	Strong transcription	Fetal Muscle Leg	muscle
25	chr6:56321000-56331200	Strong transcription	Left Ventricle	heart
26	chr6:56321000-56331800	Strong transcription	Brain Hippocampus Middle	brain
27	chr6:56321000-56343400	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr6:56321200-56343800	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr6:56321800-56331800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:56322000-56330000	Strong transcription	Brain Cingulate Gyrus	brain
31	chr6:56322000-56330800	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr6:56322000-56331600	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr6:56322000-56332400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr6:56322200-56331400	Strong transcription	Duodenum Mucosa	Duodenum
35	chr6:56322200-56332200	Strong transcription	GM12878-XiMat	blood
36	chr6:56322200-56339000	Strong transcription	Skeletal Muscle Female	skeletal muscle
37	chr6:56322200-56349200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr6:56322400-56344200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr6:56322600-56348200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:56322800-56331000	Strong transcription	HepG2	liver
41	chr6:56323000-56331800	Strong transcription	HMEC	breast
42	chr6:56323600-56331200	Strong transcription	Colon Smooth Muscle	Colon
43	chr6:56324000-56333600	Weak transcription	Psoas Muscle	Psoas
44	chr6:56324200-56329200	Weak transcription	Esophagus	oesophagus
45	chr6:56324200-56331200	Strong transcription	Brain Angular Gyrus	brain
46	chr6:56324600-56328400	Weak transcription	A549	lung
47	chr6:56324600-56331600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr6:56324800-56336800	Weak transcription	Gastric	stomach
49	chr6:56324800-56340400	Weak transcription	Spleen	Spleen
50	chr6:56325000-56328200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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