Variant report

Variant	nsv873635
Chromosome Location	chr2:10286466-10344465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:842)
CpG islands
(count:488)
Chromatin interactive
region (count:76)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:10341458-10341771	HepG2	liver:	n/a	n/a
2	BACH1	chr2:10337360-10337392	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:10295926-10296066	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr2:10304004-10304282	GM12878	blood:	n/a	n/a
5	BCL3	chr2:10303971-10304341	GM12878	blood:	n/a	n/a
6	BCL3	chr2:10301526-10301913	GM12878	blood:	n/a	n/a
7	BCL3	chr2:10302272-10302677	GM12878	blood:	n/a	n/a
8	BCL3	chr2:10302244-10302654	GM12878	blood:	n/a	n/a
9	BCL3	chr2:10301589-10301903	GM12878	blood:	n/a	n/a
10	BCL3	chr2:10295787-10296033	GM12878	blood:	n/a	n/a
11	BRCA1	chr2:10308895-10308938	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr2:10338673-10338916	K562	blood:	n/a	n/a
13	CBX3	chr2:10338593-10338919	K562	blood:	n/a	n/a
14	CCNT2	chr2:10302362-10302387	K562	blood:	n/a	n/a
15	CEBPB	chr2:10315760-10315783	K562	blood:	n/a	n/a
16	CEBPB	chr2:10312763-10312862	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:10341507-10341776	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:10310366-10310700	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:10293222-10293287	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:10293144-10293279	A549	lung:	n/a	n/a
21	CTCF	chr2:10328476-10328640	Fibrobl	skin:	n/a	n/a
22	CTCF	chr2:10297500-10297650	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr2:10297460-10297610	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr2:10328440-10328590	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr2:10303540-10303690	HAc	cerebellar:	n/a	n/a
26	CTCF	chr2:10297460-10297610	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr2:10328454-10328631	Gliobla	brain:	n/a	n/a
28	CTCF	chr2:10328400-10328550	A549	lung:	n/a	n/a
29	CTCF	chr2:10328294-10328750	A549	lung:	n/a	n/a
30	CTCF	chr2:10303440-10303590	MCF-7	breast:	n/a	chr2:10303510-10303518 chr2:10303511-10303524 chr2:10303508-10303526
31	CTCF	chr2:10297512-10297518	GM13977	blood:	n/a	n/a
32	CTCF	chr2:10303523-10303580	Fibrobl	skin:	n/a	n/a
33	CTCF	chr2:10328400-10328550	HRE	kidney:	n/a	n/a
34	CTCF	chr2:10336599-10336601	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:10328432-10328630	ProgFib	skin:	n/a	n/a
36	CTCF	chr2:10328460-10328610	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr2:10328420-10328570	GM12864	blood:	n/a	n/a
38	CTCF	chr2:10303490-10303612	Medullo	brain:	n/a	chr2:10303510-10303518 chr2:10303511-10303524 chr2:10303508-10303526
39	CTCF	chr2:10297489-10297635	HepG2	liver:	n/a	n/a
40	CTCF	chr2:10328480-10328630	GM12874	blood:	n/a	n/a
41	CTCF	chr2:10328420-10328570	BE2_C	brain:	n/a	n/a
42	CTCF	chr2:10328312-10328872	HCT-116	colon:	n/a	n/a
43	CTCF	chr2:10328480-10328630	HMF	breast:	n/a	n/a
44	CTCF	chr2:10303459-10303594	Hela-S3	cervix:	n/a	chr2:10303510-10303518 chr2:10303511-10303524 chr2:10303508-10303526
45	CTCF	chr2:10336420-10336570	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr2:10297500-10297650	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr2:10303460-10303610	HPAF	blood vessel:	n/a	chr2:10303510-10303518 chr2:10303511-10303524 chr2:10303508-10303526
48	CTCF	chr2:10303500-10303650	AG04449	skin:	n/a	chr2:10303510-10303518 chr2:10303511-10303524 chr2:10303508-10303526
49	CTCF	chr2:10309448-10309464	GM12878	blood:	n/a	n/a
50	CTCF	chr2:10336480-10336630	SK-N-SH_RA	brain:	n/a	chr2:10336576-10336589

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10334372-10334422	Caco-2	colon:	n/a
2	chr2:10302454-10302504	H1-hESC	embryonic stem cell:	embryo
3	chr2:10334372-10334422	HUVEC	blood vessel:	n/a
4	chr2:10334372-10334422	MCF-7	breast:	n/a
5	chr2:10340837-10340887	AG04450	lung:	fetal
6	chr2:10302462-10302512	SK-N-SH	brain:	n/a
7	chr2:10310255-10310305	NHDF-neo	bronchial:	n/a
8	chr2:10340653-10340703	AG04449	skin:	fetal
9	chr2:10302462-10302512	GM06990	blood:	n/a
10	chr2:10302391-10302441	HL-60	blood:	n/a
11	chr2:10340837-10340887	AG09319	gingival:	n/a
12	chr2:10302454-10302504	BE2_C	brain:	n/a
13	chr2:10302454-10302504	HMEC	breast:	n/a
14	chr2:10334372-10334422	ProgFib	skin:	n/a
15	chr2:10340558-10340608	HCM	heart:	n/a
16	chr2:10334372-10334422	GM12891	blood:	n/a
17	chr2:10340837-10340887	HRE	kidney:	n/a
18	chr2:10340558-10340608	SKMC	muscle:	n/a
19	chr2:10340653-10340703	PANC-1	pancreas:	n/a
20	chr2:10310255-10310305	HUVEC	blood vessel:	n/a
21	chr2:10340837-10340887	NB4	blood:	n/a
22	chr2:10310255-10310305	HAEpiC	amniotic membrane:	n/a
23	chr2:10340558-10340608	NB4	blood:	n/a
24	chr2:10340558-10340608	HCF	heart:	n/a
25	chr2:10340653-10340703	BE2_C	brain:	n/a
26	chr2:10302391-10302441	PANC-1	pancreas:	n/a
27	chr2:10340837-10340887	SKMC	muscle:	n/a
28	chr2:10302462-10302512	Caco-2	colon:	n/a
29	chr2:10340653-10340703	GM19239	blood:	n/a
30	chr2:10302454-10302504	CMK	blood:	n/a
31	chr2:10340837-10340887	HUVEC	blood vessel:	n/a
32	chr2:10334372-10334422	HEEpiC	esophagus:	n/a
33	chr2:10334372-10334422	NH-A	brain:	n/a
34	chr2:10340558-10340608	NHDF-neo	bronchial:	n/a
35	chr2:10310255-10310305	MCF10A-Er-Src	breast:	n/a
36	chr2:10302454-10302504	NHBE	bronchial:	n/a
37	chr2:10302462-10302512	AG04449	skin:	fetal
38	chr2:10302391-10302441	HepG2	liver:	n/a
39	chr2:10302462-10302512	ECC-1	luminal epithelium:	n/a
40	chr2:10340837-10340887	BJ	skin:	n/a
41	chr2:10340653-10340703	PrEC	prostate:	n/a
42	chr2:10302454-10302504	Hela-S3	cervix:	n/a
43	chr2:10334372-10334422	A549	lung:	n/a
44	chr2:10302391-10302441	HUVEC	blood vessel:	n/a
45	chr2:10340558-10340608	Hepatocyte	liver:	n/a
46	chr2:10302391-10302441	HNPCEpiC	eye:	n/a
47	chr2:10302454-10302504	Caco-2	colon:	n/a
48	chr2:10340837-10340887	CMK	blood:	n/a
49	chr2:10310255-10310305	LNCaP	prostate:	n/a
50	chr2:10302454-10302504	MCF-7	breast:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:10292229..10297354-chr2:10297861..10300566,4	K562	blood:
2	chr2:10333609..10335207-chr2:10346879..10348820,2	K562	blood:
3	chr2:10328455..10329154-chr2:10549215..10549757,2	K562	blood:
4	chr2:10285048..10287112-chr2:10288581..10290154,2	K562	blood:
5	chr2:10302897..10304868-chr2:10308947..10311458,3	K562	blood:
6	chr2:10275050..10276633-chr2:10298060..10300888,2	K562	blood:
7	chr2:10328421..10328930-chr2:10442179..10443004,2	MCF-7	breast:
8	chr2:10328150..10328991-chr2:10548904..10549863,5	MCF-7	breast:
9	chr2:10305391..10309576-chr2:10311864..10315375,4	K562	blood:
10	chr2:10311566..10313814-chr2:10315451..10318799,4	K562	blood:
11	chr2:10302901..10305330-chr2:10325922..10328605,2	K562	blood:
12	chr2:10303041..10305346-chr2:10310124..10311738,2	MCF-7	breast:
13	chr2:10280945..10282469-chr2:10297115..10299071,2	MCF-7	breast:
14	chr2:10318881..10321554-chr2:10323338..10324897,2	MCF-7	breast:
15	chr2:10320031..10321774-chr2:10324619..10326821,2	K562	blood:
16	chr2:10289232..10291569-chr2:10295558..10297132,2	K562	blood:
17	chr2:10306251..10307952-chr2:10309148..10311795,2	K562	blood:
18	chr2:10296675..10298215-chr2:10573676..10576663,2	K562	blood:
19	chr2:10344349..10346575-chr2:10349485..10351710,2	MCF-7	breast:
20	chr2:10325813..10327549-chr2:10329142..10331851,2	K562	blood:
21	chr2:10328469..10328995-chr2:10574784..10575648,2	MCF-7	breast:
22	chr2:10302901..10305330-chr2:10325922..10328605,2	K562	blood:
23	chr2:10306251..10307952-chr2:10309148..10311795,2	K562	blood:
24	chr2:10318881..10321554-chr2:10323338..10324897,2	MCF-7	breast:
25	chr2:10302897..10304868-chr2:10308947..10311458,3	K562	blood:
26	chr2:10333815..10336556-chr2:10366578..10368507,2	MCF-7	breast:
27	chr2:10311566..10313814-chr2:10315451..10318799,4	K562	blood:
28	chr16:2902125..2904816-chr2:10333422..10334922,2	MCF-7	breast:
29	chr2:10325813..10328227-chr2:10329027..10331851,2	K562	blood:
30	chr2:10284792..10287057-chr2:10444307..10446479,2	K562	blood:
31	chr2:10306251..10307952-chr2:10310022..10311795,2	K562	blood:
32	chr2:10307132..10308856-chr2:10309246..10312137,2	MCF-7	breast:
33	chr2:10328447..10328994-chr2:10426584..10427446,2	MCF-7	breast:
34	chr2:10292318..10295172-chr2:10445381..10448141,2	K562	blood:
35	chr2:10297096..10298028-chr2:10575136..10575688,2	K562	blood:
36	chr2:10260668..10263608-chr2:10310509..10313145,2	K562	blood:
37	chr2:10326584..10329033-chr2:10441051..10443274,2	MCF-7	breast:
38	chr2:10326687..10328532-chr2:10350704..10352850,2	K562	blood:
39	chr2:10280390..10283341-chr2:10285489..10288110,3	MCF-7	breast:
40	chr2:10272274..10274991-chr2:10298937..10301947,3	K562	blood:
41	chr2:10328419..10328932-chr2:10445333..10446204,3	MCF-7	breast:
42	chr2:10299807..10303440-chr2:10586234..10589711,3	K562	blood:
43	chr2:10289232..10291569-chr2:10295558..10297132,2	K562	blood:
44	chr2:10307132..10308856-chr2:10309246..10312137,2	MCF-7	breast:
45	chr2:10272209..10275438-chr2:10333614..10336814,3	K562	blood:
46	chr2:10339278..10341450-chr2:10342848..10344717,2	K562	blood:
47	chr2:10328063..10328629-chr2:10575089..10575716,3	K562	blood:
48	chr2:10299318..10302918-chr2:10305124..10307341,4	K562	blood:
49	chr2:10305391..10309576-chr2:10311864..10315375,4	K562	blood:
50	chr2:10335310..10337198-chr2:10565374..10566915,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYS1-7	chr2:10341367-10341629	NONHSAT069093
2	lnc-CYS1-7	chr2:10338881-10339400	NONHSAT069093

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4261	chr2:10332750-10332765	MIMAT0016890

No data

Variant related genes	Relation type
ENSG00000206647	TF binding region
MIR4261	TF binding region
ENSG00000206647	CpG island
MIR4261	CpG island
ENSG00000115756	chromatin interactions
ENSG00000206633	chromatin interactions
ENSG00000163009	chromatin interactions
ENSG00000265418	chromatin interactions
ENSG00000257135	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000206647	chromatin interactions
ENSG00000115758	chromatin interactions
ENSG00000171848	chromatin interactions

Extended variants
information (count: 2485 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2485 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6749325	chr2:10286466-10286467	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539217330	chr2:10286500-10286501	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190506610	chr2:10286515-10286516	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs146226510	chr2:10286552-10286553	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560364148	chr2:10286560-10286561	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573812712	chr2:10286574-10286575	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182393105	chr2:10286611-10286612	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs367705700	chr2:10286622-10286623	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562400220	chr2:10286629-10286630	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs79676633	chr2:10286658-10286659	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs551059109	chr2:10286669-10286670	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs564464341	chr2:10286705-10286706	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139146617	chr2:10286717-10286718	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs73169311	chr2:10286735-10286736	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs4669531	chr2:10286746-10286747	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs371337936	chr2:10286779-10286780	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs397770871	chr2:10286782-10286783	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs115675631	chr2:10286805-10286806	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs6707144	chr2:10286826-10286827	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs113288121	chr2:10286867-10286868	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538253971	chr2:10286897-10286898	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558153846	chr2:10286915-10286916	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372532075	chr2:10286926-10286927	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs35040914	chr2:10286933-10286934	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs578018067	chr2:10286963-10286964	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs149939010	chr2:10287077-10287078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs144125930	chr2:10287081-10287082	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575803476	chr2:10287085-10287086	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573784669	chr2:10287089-10287090	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs6707406	chr2:10287091-10287092	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544380726	chr2:10287124-10287125	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs184702986	chr2:10287169-10287170	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369690280	chr2:10287182-10287183	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs148681090	chr2:10287220-10287221	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544633132	chr2:10287261-10287262	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs13010608	chr2:10287269-10287270	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs12987867	chr2:10287296-10287297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs546886613	chr2:10287307-10287308	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs559678805	chr2:10287313-10287314	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529498115	chr2:10287330-10287331	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs376315691	chr2:10287355-10287356	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189120700	chr2:10287373-10287374	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369626853	chr2:10287403-10287404	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181438067	chr2:10287407-10287408	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371592550	chr2:10287408-10287409	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34176911	chr2:10287415-10287416	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185776065	chr2:10287475-10287476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571657666	chr2:10287522-10287523	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs147863532	chr2:10287552-10287553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554119789	chr2:10287591-10287592	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10269600-10299400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr2:10271400-10303800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:10272600-10289800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:10273800-10289800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:10273800-10330400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:10274000-10299200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:10276400-10307400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr2:10276600-10301800	Weak transcription	Osteobl	bone
9	chr2:10277600-10321600	Weak transcription	K562	blood
10	chr2:10277800-10295400	Weak transcription	Hela-S3	cervix
11	chr2:10278000-10302200	Weak transcription	HSMM	muscle
12	chr2:10278000-10311800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:10279400-10292000	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr2:10279600-10295600	Weak transcription	Fetal Brain Female	brain
15	chr2:10280800-10287000	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr2:10281000-10292400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:10281000-10294200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:10281600-10287000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr2:10281800-10287000	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr2:10282000-10286800	Strong transcription	Cortex derived primary cultured neurospheres	brain
21	chr2:10282000-10287800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:10282200-10290200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr2:10282200-10316600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr2:10282400-10287000	Strong transcription	Thymus	Thymus
25	chr2:10282400-10289800	Strong transcription	Dnd41	blood
26	chr2:10283000-10289200	Strong transcription	Fetal Thymus	thymus
27	chr2:10283000-10289600	Weak transcription	Primary T cells from cord blood	blood
28	chr2:10283400-10287000	Strong transcription	H1 Cell Line	embryonic stem cell
29	chr2:10283400-10287800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:10283600-10286600	Strong transcription	HepG2	liver
31	chr2:10283600-10289800	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr2:10283800-10289800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr2:10284000-10286800	Strong transcription	GM12878-XiMat	blood
34	chr2:10284400-10286600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:10284400-10288800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr2:10284400-10289800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr2:10284400-10299400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr2:10284600-10295400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr2:10285000-10287000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr2:10285000-10299400	Weak transcription	Fetal Lung	lung
41	chr2:10285200-10286800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr2:10285200-10286800	Genic enhancers	Fetal Muscle Trunk	muscle
43	chr2:10285200-10289800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr2:10285200-10299800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:10285400-10302000	Weak transcription	HMEC	breast
46	chr2:10285600-10286800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr2:10285600-10287000	Strong transcription	NHEK	skin
48	chr2:10285600-10287800	Strong transcription	A549	lung
49	chr2:10285600-10307400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr2:10285800-10287800	Strong transcription	Fetal Intestine Small	intestine

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