Variant report

Variant	nsv581752
Chromosome Location	chr2:47248111-47262137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:640)
CpG islands
(count:123)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:47260134-47260492	HepG2	liver:	n/a	chr2:47260343-47260359
2	ARID3A	chr2:47261233-47262708	HepG2	liver:	n/a	n/a
3	ATF3	chr2:47260956-47262054	A549	lung:	n/a	n/a
4	ATF3	chr2:47261061-47261966	A549	lung:	n/a	n/a
5	BCL3	chr2:47260971-47262534	A549	lung:	n/a	chr2:47261600-47261607
6	BCL3	chr2:47260131-47262418	A549	lung:	n/a	chr2:47261600-47261607
7	BHLHE40	chr2:47260184-47262789	HepG2	liver:	n/a	chr2:47262041-47262050 chr2:47262042-47262051 chr2:47262041-47262050
8	BHLHE40	chr2:47261113-47262118	A549	lung:	n/a	chr2:47262041-47262050 chr2:47262042-47262051 chr2:47262041-47262050
9	BHLHE40	chr2:47261187-47261624	HepG2	liver:	n/a	n/a
10	BHLHE40	chr2:47261256-47261837	HepG2	liver:	n/a	n/a
11	BHLHE40	chr2:47261297-47261625	K562	blood:	n/a	n/a
12	BRCA1	chr2:47261033-47261936	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr2:47260648-47262049	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:47261560-47261984	A549	lung:	n/a	n/a
15	CEBPB	chr2:47261531-47262025	MCF-7	breast:	n/a	n/a
16	CEBPB	chr2:47251266-47251441	Hela-S3	cervix:	n/a	chr2:47251319-47251330 chr2:47251316-47251333
17	CEBPB	chr2:47259592-47259821	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr2:47261029-47262305	A549	lung:	n/a	n/a
19	CEBPB	chr2:47261161-47261954	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:47261239-47262012	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:47251242-47251442	HepG2	liver:	n/a	chr2:47251319-47251330 chr2:47251316-47251333
22	CEBPB	chr2:47261248-47261969	A549	lung:	n/a	n/a
23	CEBPB	chr2:47257364-47257434	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:47251214-47251435	IMR90	lung:	n/a	chr2:47251319-47251330 chr2:47251316-47251333
25	CEBPB	chr2:47261627-47261889	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:47261259-47262021	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr2:47261277-47261975	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:47257276-47257498	A549	lung:	n/a	n/a
29	CEBPB	chr2:47258260-47258303	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:47251157-47251431	A549	lung:	n/a	chr2:47251319-47251330 chr2:47251316-47251333
31	CEBPB	chr2:47261279-47262027	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:47261315-47261512	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:47261216-47262017	Hela-S3	cervix:	n/a	n/a
34	CEBPD	chr2:47261274-47261665	HepG2	liver:	n/a	n/a
35	CEBPD	chr2:47261199-47262028	HepG2	liver:	n/a	n/a
36	CHD2	chr2:47261255-47262290	HepG2	liver:	n/a	n/a
37	CHD2	chr2:47260789-47260986	HepG2	liver:	n/a	n/a
38	CHD2	chr2:47261514-47261821	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr2:47261229-47262018	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr2:47261145-47262069	A549	lung:	n/a	n/a
41	CTCF	chr2:47260420-47260570	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr2:47261280-47261430	GM12875	blood:	n/a	n/a
43	CTCF	chr2:47261340-47261490	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr2:47261320-47261470	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr2:47261320-47261470	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:47260088-47262012	SK-N-SH	brain:	n/a	n/a
47	CTCF	chr2:47257160-47257310	NHEK	skin:	n/a	n/a
48	CTCF	chr2:47261320-47261470	GM12866	blood:	n/a	n/a
49	CTCF	chr2:47261200-47261350	GM12864	blood:	n/a	n/a
50	CTCF	chr2:47261239-47261574	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:47261900-47261950	ovcar-3	ovarian:	n/a
2	chr2:47261900-47261950	ovcar-3	ovarian:	n/a
3	chr2:47261900-47261950	HRE	kidney:	n/a
4	chr2:47257584-47257634	CMK	blood:	n/a
5	chr2:47261900-47261950	AG09309	skin:	n/a
6	chr2:47261900-47261950	SK-N-MC	brain:	n/a
7	chr2:47261900-47261950	SKMC	muscle:	n/a
8	chr2:47257584-47257634	U87	brain:	n/a
9	chr2:47261900-47261950	U87	brain:	n/a
10	chr2:47257584-47257634	NB4	blood:	n/a
11	chr2:47257584-47257634	SK-N-MC	brain:	n/a
12	chr2:47261900-47261950	NHBE	bronchial:	n/a
13	chr2:47261900-47261950	NHDF-neo	bronchial:	n/a
14	chr2:47257584-47257634	HCPEpiC	choroid plexus:	n/a
15	chr2:47261900-47261950	HMEC	breast:	n/a
16	chr2:47257584-47257634	NH-A	brain:	n/a
17	chr2:47261900-47261950	AG09319	gingival:	n/a
18	chr2:47257584-47257634	PFSK-1	brain:	n/a
19	chr2:47257584-47257634	HRCEpiC	kidney:	n/a
20	chr2:47257584-47257634	SK-N-SH_RA	brain:	n/a
21	chr2:47261900-47261950	PANC-1	pancreas:	n/a
22	chr2:47261900-47261950	PrEC	prostate:	n/a
23	chr2:47261900-47261950	BE2_C	brain:	n/a
24	chr2:47257584-47257634	Jurkat	blood:	n/a
25	chr2:47261900-47261950	ProgFib	skin:	n/a
26	chr2:47261900-47261950	Hepatocyte	liver:	n/a
27	chr2:47257584-47257634	AG04450	lung:	fetal
28	chr2:47257584-47257634	MCF-7	breast:	n/a
29	chr2:47257584-47257634	MCF10A-Er-Src	breast:	n/a
30	chr2:47261900-47261950	HCM	heart:	n/a
31	chr2:47257584-47257634	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:47261900-47261950	Caco-2	colon:	n/a
33	chr2:47261900-47261950	HEEpiC	esophagus:	n/a
34	chr2:47261900-47261950	HCF	heart:	n/a
35	chr2:47257584-47257634	PrEC	prostate:	n/a
36	chr2:47257584-47257634	AG09309	skin:	n/a
37	chr2:47261900-47261950	ECC-1	luminal epithelium:	n/a
38	chr2:47261900-47261950	AG10803	skin:	n/a
39	chr2:47261900-47261950	AoSMC	blood vessel:	n/a
40	chr2:47261900-47261950	HEK293	kidney:	embryo
41	chr2:47257584-47257634	AG04449	skin:	fetal
42	chr2:47257584-47257634	K562	blood:	n/a
43	chr2:47261900-47261950	HCPEpiC	choroid plexus:	n/a
44	chr2:47257584-47257634	Hepatocyte	liver:	n/a
45	chr2:47261900-47261950	K562	blood:	n/a
46	chr2:47261900-47261950	HIPEpiC	eye:	n/a
47	chr2:47261900-47261950	BJ	skin:	n/a
48	chr2:47261900-47261950	IMR90	lung:	fetal
49	chr2:47257584-47257634	HRPEpiC	eye:	n/a
50	chr2:47257584-47257634	H1-hESC	embryonic stem cell:	embryo

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:47246848..47248803-chr2:47402260..47405081,2	MCF-7	breast:
2	chr2:47251517..47253255-chr2:47403256..47405239,2	K562	blood:
3	chr2:47252232..47263251-chr2:47397787..47406051,20	MCF-7	breast:
4	chr2:47250659..47252384-chr2:47268724..47270646,2	MCF-7	breast:
5	chr2:47213985..47214817-chr2:47255980..47256485,2	MCF-7	breast:
6	chr2:47253562..47255469-chr2:47401214..47402778,2	K562	blood:
7	chr2:47247505..47249498-chr2:47258978..47261043,2	K562	blood:
8	chr2:47256246..47258150-chr2:47393234..47395385,2	MCF-7	breast:
9	chr2:47246848..47250170-chr2:47255935..47259327,3	MCF-7	breast:
10	chr2:47258480..47260174-chr2:47263659..47266616,2	K562	blood:
11	chr2:47257326..47259699-chr2:47417975..47420606,2	MCF-7	breast:
12	chr2:47214073..47216296-chr2:47255513..47257887,2	MCF-7	breast:
13	chr2:47246848..47250170-chr2:47255935..47259327,3	MCF-7	breast:
14	chr2:47248098..47250499-chr2:47402045..47403673,2	K562	blood:
15	chr2:47247292..47249498-chr2:47258978..47261257,2	K562	blood:
16	chr2:47255748..47256619-chr2:47382340..47383007,2	MCF-7	breast:
17	chr2:47249673..47251618-chr2:47253667..47255571,2	MCF-7	breast:
18	chr2:47262016..47264669-chr2:47272967..47274595,2	MCF-7	breast:
19	chr2:47252397..47254046-chr2:47254810..47257644,2	K562	blood:
20	chr2:47252454..47254562-chr2:47258233..47260100,2	K562	blood:
21	chr2:47197939..47198482-chr2:47256135..47256820,3	MCF-7	breast:
22	chr2:47242011..47245119-chr2:47248786..47251159,3	K562	blood:
23	chr2:47246499..47248286-chr2:47253507..47255645,2	MCF-7	breast:
24	chr2:47227819..47229844-chr2:47253559..47255515,2	K562	blood:
25	chr2:47247534..47249636-chr2:47250357..47252583,2	MCF-7	breast:
26	chr2:47249673..47251618-chr2:47253667..47255571,2	MCF-7	breast:
27	chr17:57919156..57921575-chr2:47249552..47252093,2	MCF-7	breast:
28	chr2:47243930..47246637-chr2:47261701..47264377,2	MCF-7	breast:
29	chr2:47261315..47264096-chr2:47264626..47268326,4	K562	blood:
30	chr2:47247534..47249636-chr2:47250357..47252583,2	MCF-7	breast:
31	chr2:47247505..47249498-chr2:47258978..47261043,2	K562	blood:
32	chr2:47247796..47250364-chr2:47260163..47262120,2	MCF-7	breast:
33	chr2:47252454..47254562-chr2:47258233..47260100,2	K562	blood:
34	chr2:47197790..47198513-chr2:47256135..47256820,5	MCF-7	breast:
35	chr2:47252113..47260352-chr2:47399089..47405669,11	MCF-7	breast:
36	chr2:47257664..47259808-chr2:47380368..47382770,2	MCF-7	breast:
37	chr2:47247292..47249498-chr2:47258978..47261257,2	K562	blood:
38	chr2:47252397..47254046-chr2:47254810..47257644,2	K562	blood:
39	chr2:47246499..47248286-chr2:47253507..47255645,2	MCF-7	breast:
40	chr2:47260087..47265958-chr2:47400378..47404964,8	K562	blood:
41	chr2:47239533..47242401-chr2:47254885..47256539,3	MCF-7	breast:
42	chr2:47255574..47257278-chr2:47259885..47262274,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALM2-5	chr2:47253515-47254279	expReg_chr2_3631_-
2	lnc-CALM2-6	chr2:47253068-47253374	expReg_chr2_3630_-

No data

Variant related genes	Relation type
TTC7A	TF binding region
TTC7A	CpG island
ENSG00000068724	chromatin interactions
ENSG00000143933	chromatin interactions
ENSG00000239605	chromatin interactions
ENSG00000233845	chromatin interactions

Extended variants
information (count: 760 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs919883	chr2:47248111-47248112	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs55654462	chr2:47248125-47248126	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs191169592	chr2:47248140-47248141	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs112411396	chr2:47248163-47248164	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs919884	chr2:47248196-47248197	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs77095003	chr2:47248198-47248199	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs570556865	chr2:47248232-47248233	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs569067939	chr2:47248235-47248236	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs139903882	chr2:47248244-47248245	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs551608631	chr2:47248246-47248247	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374376666	chr2:47248268-47248269	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs111777698	chr2:47248272-47248273	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372015423	chr2:47248276-47248277	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534164725	chr2:47248301-47248302	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs1978744	chr2:47248334-47248335	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573826279	chr2:47248348-47248349	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs537947113	chr2:47248354-47248355	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs556380074	chr2:47248385-47248386	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370566513	chr2:47248393-47248394	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs545381314	chr2:47248400-47248401	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs183933345	chr2:47248427-47248428	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs546733236	chr2:47248439-47248440	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs572765419	chr2:47248464-47248465	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs7565217	chr2:47248466-47248467	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs561644553	chr2:47248483-47248484	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529043348	chr2:47248497-47248498	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534733492	chr2:47248505-47248506	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs74613802	chr2:47248548-47248549	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs34943402	chr2:47248550-47248551	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs4511767	chr2:47248615-47248616	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs551404741	chr2:47248654-47248655	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs72872951	chr2:47248661-47248662	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs10205984	chr2:47248702-47248703	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs34029850	chr2:47248726-47248727	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs13000736	chr2:47248727-47248728	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs7592145	chr2:47248745-47248746	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs556193077	chr2:47248755-47248756	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs571769257	chr2:47248776-47248777	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs112336794	chr2:47248791-47248792	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539188314	chr2:47248803-47248804	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs142122564	chr2:47248815-47248816	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs386645747	chr2:47248833-47248834	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs7565683	chr2:47248834-47248835	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs377291733	chr2:47248851-47248852	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187254929	chr2:47248857-47248858	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544325161	chr2:47248873-47248874	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs199554408	chr2:47248913-47248914	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562538735	chr2:47248920-47248921	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532873753	chr2:47248921-47248922	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112546104	chr2:47248923-47248924	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Breast cancer	17603634	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
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Myelofibrosis	22110671	CNVD
Hypotonia	17579669	CNVD
Hypotonia-Cystinuria syndrome	16385448	CNVD
Glioblastoma multiforme	17002787	CNVD
Cystinuria	17625506	CNVD
Breast cancer	16272173	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47213600-47256400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:47214000-47262000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr2:47222000-47260600	Weak transcription	Small Intestine	intestine
4	chr2:47229200-47248600	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr2:47230200-47302800	Strong transcription	Dnd41	blood
6	chr2:47232000-47265000	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr2:47232400-47257000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:47234400-47283600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr2:47236000-47278600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr2:47236600-47253600	Strong transcription	Fetal Intestine Small	intestine
11	chr2:47236600-47259200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:47236600-47259200	Weak transcription	Fetal Kidney	kidney
13	chr2:47236800-47251600	Weak transcription	Fetal Lung	lung
14	chr2:47237000-47254200	Weak transcription	Ovary	ovary
15	chr2:47237000-47260400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr2:47237200-47249200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:47238200-47253400	Strong transcription	Placenta Amnion	Placenta Amnion
18	chr2:47238200-47253600	Strong transcription	Duodenum Mucosa	Duodenum
19	chr2:47238200-47253800	Strong transcription	HepG2	liver
20	chr2:47239400-47249200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr2:47240000-47249800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr2:47240200-47251800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:47240200-47256000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr2:47240600-47248800	Weak transcription	Liver	Liver
25	chr2:47240600-47249200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr2:47240800-47251400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr2:47241400-47250400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr2:47242000-47249000	Weak transcription	Colonic Mucosa	Colon
29	chr2:47242000-47249200	Weak transcription	Brain Germinal Matrix	brain
30	chr2:47242200-47250400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:47242200-47253400	Weak transcription	HMEC	breast
32	chr2:47243800-47248600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:47243800-47248600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr2:47243800-47249200	Weak transcription	HSMMtube	muscle
35	chr2:47243800-47249800	Weak transcription	Hela-S3	cervix
36	chr2:47243800-47260200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr2:47243800-47260400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr2:47243800-47260800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:47243800-47261000	Weak transcription	K562	blood
40	chr2:47244000-47248200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr2:47244000-47249400	Weak transcription	NH-A	brain
42	chr2:47244000-47250600	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr2:47244000-47252800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr2:47244000-47253200	Weak transcription	Stomach Mucosa	stomach
45	chr2:47244000-47254200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:47244000-47256000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:47244000-47256800	Strong transcription	Osteobl	bone
48	chr2:47244000-47257200	Weak transcription	HUVEC	blood vessel
49	chr2:47244000-47258800	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr2:47244000-47260600	Weak transcription	H1 Cell Line	embryonic stem cell

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