Variant report

Variant	nsv984532
Chromosome Location	chr2:47237908-47270533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1337)
CpG islands
(count:244)
Chromatin interactive
region (count:86)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1337 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:47263245-47263597	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:47270374-47270982	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:47261233-47262708	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:47260134-47260492	HepG2	liver:	n/a	chr2:47260343-47260359
5	ATF3	chr2:47261061-47261966	A549	lung:	n/a	n/a
6	ATF3	chr2:47260956-47262054	A549	lung:	n/a	n/a
7	BCL3	chr2:47260131-47262418	A549	lung:	n/a	chr2:47261600-47261607
8	BCL3	chr2:47270082-47271383	A549	lung:	n/a	chr2:47271228-47271237
9	BCL3	chr2:47260971-47262534	A549	lung:	n/a	chr2:47261600-47261607
10	BHLHE40	chr2:47261113-47262118	A549	lung:	n/a	chr2:47262041-47262050 chr2:47262042-47262051 chr2:47262041-47262050
11	BHLHE40	chr2:47263294-47263553	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:47261297-47261625	K562	blood:	n/a	n/a
13	BHLHE40	chr2:47262460-47262786	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:47260184-47262789	HepG2	liver:	n/a	chr2:47262041-47262050 chr2:47262042-47262051 chr2:47262041-47262050
15	BHLHE40	chr2:47261187-47261624	HepG2	liver:	n/a	n/a
16	BHLHE40	chr2:47261256-47261837	HepG2	liver:	n/a	n/a
17	BHLHE40	chr2:47243785-47243967	K562	blood:	n/a	n/a
18	BRCA1	chr2:47267946-47268112	HepG2	liver:	n/a	n/a
19	BRCA1	chr2:47267567-47267708	HepG2	liver:	n/a	n/a
20	BRCA1	chr2:47243768-47243860	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr2:47260648-47262049	HepG2	liver:	n/a	n/a
22	BRCA1	chr2:47261033-47261936	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr2:47243333-47244056	HCT-116	colon:	n/a	n/a
24	CEBPB	chr2:47242417-47242617	A549	lung:	n/a	chr2:47242528-47242540
25	CEBPB	chr2:47243612-47243929	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:47257364-47257434	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:47261161-47261954	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:47261216-47262017	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:47261279-47262027	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:47261627-47261889	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:47267430-47267656	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:47268693-47268877	A549	lung:	n/a	n/a
33	CEBPB	chr2:47261531-47262025	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:47261277-47261975	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:47261259-47262021	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr2:47261239-47262012	HepG2	liver:	n/a	n/a
37	CEBPB	chr2:47258260-47258303	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:47259592-47259821	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:47267892-47268095	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:47261248-47261969	A549	lung:	n/a	n/a
41	CEBPB	chr2:47261029-47262305	A549	lung:	n/a	n/a
42	CEBPB	chr2:47251157-47251431	A549	lung:	n/a	chr2:47251319-47251330 chr2:47251316-47251333
43	CEBPB	chr2:47268773-47268924	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr2:47265014-47265105	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr2:47251266-47251441	Hela-S3	cervix:	n/a	chr2:47251319-47251330 chr2:47251316-47251333
46	CEBPB	chr2:47251214-47251435	IMR90	lung:	n/a	chr2:47251319-47251330 chr2:47251316-47251333
47	CEBPB	chr2:47261560-47261984	A549	lung:	n/a	n/a
48	CEBPB	chr2:47251242-47251442	HepG2	liver:	n/a	chr2:47251319-47251330 chr2:47251316-47251333
49	CEBPB	chr2:47257276-47257498	A549	lung:	n/a	n/a
50	CEBPB	chr2:47261315-47261512	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:47257584-47257634	BJ	skin:	n/a
2	chr2:47242277-47242327	HCPEpiC	choroid plexus:	n/a
3	chr2:47257584-47257634	A549	lung:	n/a
4	chr2:47269069-47269119	HL-60	blood:	n/a
5	chr2:47257584-47257634	GM19239	blood:	n/a
6	chr2:47261900-47261950	GM19239	blood:	n/a
7	chr2:47269069-47269119	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:47269069-47269119	ProgFib	skin:	n/a
9	chr2:47242277-47242327	NB4	blood:	n/a
10	chr2:47242277-47242327	SK-N-SH	brain:	n/a
11	chr2:47242277-47242327	HNPCEpiC	eye:	n/a
12	chr2:47269069-47269119	BJ	skin:	n/a
13	chr2:47242277-47242327	IMR90	lung:	fetal
14	chr2:47261900-47261950	RPTEC	kidney:	n/a
15	chr2:47242277-47242327	HEEpiC	esophagus:	n/a
16	chr2:47242277-47242327	HRE	kidney:	n/a
17	chr2:47269069-47269119	SK-N-SH	brain:	n/a
18	chr2:47261900-47261950	HL-60	blood:	n/a
19	chr2:47269069-47269119	AG04450	lung:	fetal
20	chr2:47242277-47242327	U87	brain:	n/a
21	chr2:47261900-47261950	Caco-2	colon:	n/a
22	chr2:47242277-47242327	T-47D	breast:	n/a
23	chr2:47242277-47242327	CMK	blood:	n/a
24	chr2:47257584-47257634	HUVEC	blood vessel:	n/a
25	chr2:47257584-47257634	HCT-116	colon:	n/a
26	chr2:47261900-47261950	HRCEpiC	kidney:	n/a
27	chr2:47257584-47257634	Jurkat	blood:	n/a
28	chr2:47261900-47261950	AG09319	gingival:	n/a
29	chr2:47261900-47261950	MCF-7	breast:	n/a
30	chr2:47257584-47257634	HL-60	blood:	n/a
31	chr2:47257584-47257634	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:47261900-47261950	AG09309	skin:	n/a
33	chr2:47269069-47269119	ECC-1	luminal epithelium:	n/a
34	chr2:47257584-47257634	HAEpiC	amniotic membrane:	n/a
35	chr2:47257584-47257634	AG04450	lung:	fetal
36	chr2:47269069-47269119	HCM	heart:	n/a
37	chr2:47257584-47257634	GM12892	blood:	n/a
38	chr2:47242277-47242327	AG09309	skin:	n/a
39	chr2:47242277-47242327	Hepatocyte	liver:	n/a
40	chr2:47261900-47261950	H1-hESC	embryonic stem cell:	embryo
41	chr2:47257584-47257634	SK-N-MC	brain:	n/a
42	chr2:47261900-47261950	GM12892	blood:	n/a
43	chr2:47269069-47269119	PANC-1	pancreas:	n/a
44	chr2:47261900-47261950	MCF10A-Er-Src	breast:	n/a
45	chr2:47269069-47269119	HEK293	kidney:	embryo
46	chr2:47261900-47261950	AG10803	skin:	n/a
47	chr2:47261900-47261950	NT2-D1	testis:	n/a
48	chr2:47242277-47242327	HRPEpiC	eye:	n/a
49	chr2:47242277-47242327	GM19239	blood:	n/a
50	chr2:47257584-47257634	GM06990	blood:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:47246499..47248286-chr2:47253507..47255645,2	MCF-7	breast:
2	chr2:47252454..47254562-chr2:47258233..47260100,2	K562	blood:
3	chr2:47267673..47270387-chr2:47397211..47399730,2	K562	blood:
4	chr2:47242011..47245119-chr2:47248786..47251159,3	K562	blood:
5	chr2:47225653..47227816-chr2:47235641..47238681,3	MCF-7	breast:
6	chr2:47262016..47264669-chr2:47272967..47274595,2	MCF-7	breast:
7	chr2:47249673..47251618-chr2:47253667..47255571,2	MCF-7	breast:
8	chr2:47237082..47239286-chr2:47241685..47244627,2	K562	blood:
9	chr2:47213985..47214817-chr2:47255980..47256485,2	MCF-7	breast:
10	chr2:47239533..47242401-chr2:47254885..47256539,3	MCF-7	breast:
11	chr2:47237082..47239286-chr2:47241685..47244627,2	K562	blood:
12	chr2:47257664..47259808-chr2:47380368..47382770,2	MCF-7	breast:
13	chr2:47260087..47265958-chr2:47400378..47404964,8	K562	blood:
14	chr2:47252232..47263251-chr2:47397787..47406051,20	MCF-7	breast:
15	chr2:47246848..47250170-chr2:47255935..47259327,3	MCF-7	breast:
16	chr2:47252397..47254046-chr2:47254810..47257644,2	K562	blood:
17	chr2:47255574..47257278-chr2:47259885..47262274,2	MCF-7	breast:
18	chr2:47248098..47250499-chr2:47402045..47403673,2	K562	blood:
19	chr2:47266042..47270456-chr2:47271373..47275642,6	K562	blood:
20	chr2:47252454..47254562-chr2:47258233..47260100,2	K562	blood:
21	chr2:47247796..47250364-chr2:47260163..47262120,2	MCF-7	breast:
22	chr2:47219377..47221556-chr2:47242383..47245078,2	MCF-7	breast:
23	chr2:47240423..47243705-chr2:47401498..47404944,5	MCF-7	breast:
24	chr2:47269944..47272346-chr2:47548303..47550473,2	MCF-7	breast:
25	chr2:47241809..47243733-chr2:47418133..47419880,2	MCF-7	breast:
26	chr17:57919156..57921575-chr2:47249552..47252093,2	MCF-7	breast:
27	chr2:47240964..47242721-chr2:47400024..47402501,2	K562	blood:
28	chr2:47269303..47271501-chr2:47388884..47391156,2	MCF-7	breast:
29	chr2:47227819..47229844-chr2:47253559..47255515,2	K562	blood:
30	chr2:47250659..47252384-chr2:47268724..47270646,2	MCF-7	breast:
31	chr2:47246091..47247839-chr2:47402201..47405168,2	K562	blood:
32	chr2:47239533..47242401-chr2:47254885..47256539,3	MCF-7	breast:
33	chr2:47262955..47263771-chr2:47304202..47304764,2	MCF-7	breast:
34	chr2:47247534..47249636-chr2:47250357..47252583,2	MCF-7	breast:
35	chr2:47269231..47272270-chr2:47291974..47297806,6	MCF-7	breast:
36	chr2:47243930..47246637-chr2:47261701..47264377,2	MCF-7	breast:
37	chr2:47238189..47239994-chr2:47402899..47405132,2	K562	blood:
38	chr2:47249673..47251618-chr2:47253667..47255571,2	MCF-7	breast:
39	chr2:47197790..47198513-chr2:47256135..47256820,5	MCF-7	breast:
40	chr2:47253562..47255469-chr2:47401214..47402778,2	K562	blood:
41	chr2:47247534..47249636-chr2:47250357..47252583,2	MCF-7	breast:
42	chr2:47235055..47237269-chr2:47239920..47242362,2	MCF-7	breast:
43	chr2:47246848..47250170-chr2:47255935..47259327,3	MCF-7	breast:
44	chr2:47252397..47254046-chr2:47254810..47257644,2	K562	blood:
45	chr2:47270183..47272803-chr2:47401195..47403585,3	K562	blood:
46	chr2:47255748..47256619-chr2:47382340..47383007,2	MCF-7	breast:
47	chr2:47247505..47249498-chr2:47258978..47261043,2	K562	blood:
48	chr2:47258480..47260174-chr2:47263659..47266616,2	K562	blood:
49	chr2:47251517..47253255-chr2:47403256..47405239,2	K562	blood:
50	chr2:47266621..47268333-chr2:47402251..47405072,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALM2-1	chr2:47267507-47267663	ENSG00000233845.1
2	lnc-CALM2-1	chr2:47262418-47262764	ENSG00000233845.1
3	lnc-CALM2-6	chr2:47253068-47253374	expReg_chr2_3630_-
4	lnc-CALM2-5	chr2:47253515-47254279	expReg_chr2_3631_-

No data

Variant related genes	Relation type
TTC7A	TF binding region
ENSG00000233845	TF binding region
TTC7A	CpG island
ENSG00000233845	CpG island
ENSG00000068724	chromatin interactions
ENSG00000233845	chromatin interactions
ENSG00000225187	chromatin interactions
ENSG00000239605	chromatin interactions
ENSG00000143933	chromatin interactions

Extended variants
information (count: 1671 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1671 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537045002	chr2:47237933-47237934	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs185938933	chr2:47237934-47237935	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550773083	chr2:47237946-47237947	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370978349	chr2:47237949-47237950	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114929024	chr2:47237968-47237969	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs138327050	chr2:47237969-47237970	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566776470	chr2:47237974-47237975	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534325129	chr2:47237984-47237985	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72806578	chr2:47237994-47237995	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs190736706	chr2:47238051-47238052	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs181822336	chr2:47238070-47238071	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs373665239	chr2:47238088-47238089	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556765592	chr2:47238092-47238093	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575414213	chr2:47238127-47238128	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs111958304	chr2:47238129-47238130	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558088773	chr2:47238154-47238155	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77652838	chr2:47238228-47238229	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs17036060	chr2:47238254-47238255	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs62138220	chr2:47238293-47238294	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186115524	chr2:47238310-47238311	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112500481	chr2:47238313-47238314	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544705457	chr2:47238343-47238344	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373646834	chr2:47238373-47238374	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562812496	chr2:47238378-47238379	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs61155978	chr2:47238383-47238384	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs551518436	chr2:47238393-47238394	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560305860	chr2:47238403-47238404	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528025943	chr2:47238434-47238435	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549244697	chr2:47238456-47238457	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568082272	chr2:47238469-47238470	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370382881	chr2:47238489-47238490	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs114202807	chr2:47238519-47238520	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs550676316	chr2:47238527-47238528	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374960733	chr2:47238529-47238530	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114276698	chr2:47238530-47238531	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147112070	chr2:47238545-47238546	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs201913059	chr2:47238546-47238547	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372929050	chr2:47238547-47238548	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558029350	chr2:47238559-47238560	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs142490773	chr2:47238564-47238565	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375540629	chr2:47238579-47238580	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368491762	chr2:47238583-47238584	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs371584761	chr2:47238591-47238592	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs55944397	chr2:47238631-47238632	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs115825693	chr2:47238660-47238661	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555663390	chr2:47238715-47238716	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574001007	chr2:47238774-47238775	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544232053	chr2:47238777-47238778	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs556627470	chr2:47238803-47238804	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs578065429	chr2:47238838-47238839	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1728 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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	chr2:47214600-47242000	Strong transcription	Thymus	Thymus
4	chr2:47214800-47239200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr2:47215200-47243800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr2:47215600-47245200	Strong transcription	Primary B cells from peripheral blood	blood
7	chr2:47216400-47241600	Strong transcription	Fetal Thymus	thymus
8	chr2:47222000-47260600	Weak transcription	Small Intestine	intestine
9	chr2:47223400-47238400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr2:47223400-47239400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr2:47223600-47239400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr2:47223600-47246800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr2:47224800-47238400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr2:47229200-47243000	Enhancers	Fetal Brain Male	brain
15	chr2:47229200-47248600	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr2:47230200-47302800	Strong transcription	Dnd41	blood
17	chr2:47230800-47243000	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr2:47231400-47242000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr2:47231400-47243000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr2:47231600-47239400	Weak transcription	NHEK	skin
21	chr2:47231600-47241200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:47231600-47243000	Strong transcription	Placenta	Placenta
23	chr2:47231600-47243000	Weak transcription	HUVEC	blood vessel
24	chr2:47231800-47243800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:47232000-47240000	Weak transcription	Hela-S3	cervix
26	chr2:47232000-47241600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:47232000-47265000	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr2:47232400-47241800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:47232400-47245000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr2:47232400-47257000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr2:47232800-47244000	Strong transcription	Esophagus	oesophagus
32	chr2:47234200-47239200	Enhancers	Colon Smooth Muscle	Colon
33	chr2:47234400-47238200	Weak transcription	Liver	Liver
34	chr2:47234400-47239000	Weak transcription	GM12878-XiMat	blood
35	chr2:47234400-47283600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr2:47234600-47238400	Weak transcription	HMEC	breast
37	chr2:47235000-47238200	Enhancers	Fetal Muscle Trunk	muscle
38	chr2:47235200-47238400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr2:47235200-47238400	Enhancers	Rectal Smooth Muscle	rectum
40	chr2:47235400-47238400	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr2:47235600-47238200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr2:47235800-47238000	Weak transcription	Primary B cells from cord blood	blood
43	chr2:47236000-47238200	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr2:47236000-47238200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr2:47236000-47238200	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr2:47236000-47243400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr2:47236000-47278600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr2:47236200-47238400	Weak transcription	Gastric	stomach
49	chr2:47236200-47241400	Weak transcription	Psoas Muscle	Psoas
50	chr2:47236200-47241800	Strong transcription	Osteobl	bone

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