Variant report

Variant	nsv874155
Chromosome Location	chr2:55205262-55307646
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3817)
CpG islands
(count:1406)
Chromatin interactive
region (count:208)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3817 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55226387-55226648	K562	blood:	n/a	n/a
2	ARID3A	chr2:55238858-55239264	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:55230697-55230715	K562	blood:	n/a	n/a
4	ARID3A	chr2:55272753-55273057	K562	blood:	n/a	n/a
5	ARID3A	chr2:55278290-55278946	K562	blood:	n/a	n/a
6	ARID3A	chr2:55307510-55307535	K562	blood:	n/a	n/a
7	ARID3A	chr2:55275681-55276548	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:55277392-55278787	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:55298252-55298504	K562	blood:	n/a	n/a
10	ARID3A	chr2:55274635-55275412	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:55280330-55280586	K562	blood:	n/a	n/a
12	ARID3A	chr2:55242106-55242431	K562	blood:	n/a	n/a
13	ARID3A	chr2:55279271-55279456	K562	blood:	n/a	n/a
14	ARID3A	chr2:55294315-55294406	K562	blood:	n/a	n/a
15	ARID3A	chr2:55253309-55253847	HepG2	liver:	n/a	n/a
16	ARID3A	chr2:55287045-55287345	K562	blood:	n/a	n/a
17	ARID3A	chr2:55275830-55276436	K562	blood:	n/a	n/a
18	ARID3A	chr2:55262695-55263033	K562	blood:	n/a	n/a
19	ARID3A	chr2:55277445-55278076	K562	blood:	n/a	n/a
20	ARID3A	chr2:55265811-55266276	K562	blood:	n/a	n/a
21	ARID3A	chr2:55273872-55274316	HepG2	liver:	n/a	n/a
22	ARID3A	chr2:55283190-55283600	K562	blood:	n/a	n/a
23	ARID3A	chr2:55263969-55264015	K562	blood:	n/a	n/a
24	ARID3A	chr2:55242061-55242915	HepG2	liver:	n/a	n/a
25	ATF1	chr2:55278339-55278652	K562	blood:	n/a	n/a
26	ATF1	chr2:55277375-55278083	K562	blood:	n/a	n/a
27	ATF1	chr2:55260581-55260769	K562	blood:	n/a	n/a
28	ATF1	chr2:55283205-55283564	K562	blood:	n/a	n/a
29	ATF2	chr2:55222644-55223045	GM12878	blood:	n/a	n/a
30	ATF2	chr2:55276004-55276422	GM12878	blood:	n/a	n/a
31	ATF2	chr2:55222675-55223161	GM12878	blood:	n/a	n/a
32	ATF2	chr2:55251981-55253064	GM12878	blood:	n/a	n/a
33	ATF2	chr2:55260165-55260956	GM12878	blood:	n/a	n/a
34	ATF2	chr2:55275822-55276750	GM12878	blood:	n/a	n/a
35	ATF2	chr2:55277224-55278047	GM12878	blood:	n/a	n/a
36	ATF2	chr2:55260247-55260863	GM12878	blood:	n/a	n/a
37	ATF2	chr2:55236793-55237829	GM12878	blood:	n/a	n/a
38	ATF2	chr2:55281235-55282115	GM12878	blood:	n/a	n/a
39	ATF2	chr2:55275625-55276754	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr2:55277366-55277757	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr2:55277397-55277783	GM12878	blood:	n/a	n/a
42	ATF3	chr2:55277314-55277972	K562	blood:	n/a	n/a
43	ATF3	chr2:55283116-55283588	K562	blood:	n/a	n/a
44	ATF3	chr2:55277965-55278806	A549	lung:	n/a	chr2:55277985-55277994
45	ATF3	chr2:55274252-55274646	K562	blood:	n/a	n/a
46	ATF3	chr2:55278147-55278717	K562	blood:	n/a	n/a
47	ATF3	chr2:55277903-55278792	A549	lung:	n/a	chr2:55277985-55277994
48	ATF3	chr2:55277283-55277897	A549	lung:	n/a	n/a
49	ATF3	chr2:55275553-55276828	A549	lung:	n/a	n/a
50	BACH1	chr2:55265645-55266072	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55239331-55239381	AG10803	skin:	n/a
2	chr2:55226987-55227037	NH-A	brain:	n/a
3	chr2:55276456-55276506	HCT-116	colon:	n/a
4	chr2:55239331-55239381	AG10803	skin:	n/a
5	chr2:55226987-55227037	NH-A	brain:	n/a
6	chr2:55276456-55276506	HCT-116	colon:	n/a
7	chr2:55276456-55276506	PANC-1	pancreas:	n/a
8	chr2:55277572-55277622	PrEC	prostate:	n/a
9	chr2:55278118-55278168	GM12892	blood:	n/a
10	chr2:55276186-55276236	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:55278043-55278093	AG09319	gingival:	n/a
12	chr2:55232193-55232243	ProgFib	skin:	n/a
13	chr2:55217063-55217113	PANC-1	pancreas:	n/a
14	chr2:55232193-55232243	Jurkat	blood:	n/a
15	chr2:55289112-55289162	NHBE	bronchial:	n/a
16	chr2:55289198-55289248	Jurkat	blood:	n/a
17	chr2:55226987-55227037	HRCEpiC	kidney:	n/a
18	chr2:55278043-55278093	BJ	skin:	n/a
19	chr2:55217063-55217113	T-47D	breast:	n/a
20	chr2:55276456-55276506	SAEC	small airway:	n/a
21	chr2:55232193-55232243	HCT-116	colon:	n/a
22	chr2:55232193-55232243	HRCEpiC	kidney:	n/a
23	chr2:55232193-55232243	PrEC	prostate:	n/a
24	chr2:55278269-55278319	HRCEpiC	kidney:	n/a
25	chr2:55276186-55276236	AG10803	skin:	n/a
26	chr2:55266232-55266282	K562	blood:	n/a
27	chr2:55266232-55266282	NHDF-neo	bronchial:	n/a
28	chr2:55217063-55217113	BJ	skin:	n/a
29	chr2:55289198-55289248	HEK293	kidney:	embryo
30	chr2:55276516-55276566	GM12891	blood:	n/a
31	chr2:55226987-55227037	HRPEpiC	eye:	n/a
32	chr2:55289198-55289248	NH-A	brain:	n/a
33	chr2:55266232-55266282	SK-N-SH	brain:	n/a
34	chr2:55276306-55276356	AG04449	skin:	fetal
35	chr2:55246602-55246652	PFSK-1	brain:	n/a
36	chr2:55276456-55276506	SK-N-SH_RA	brain:	n/a
37	chr2:55276456-55276506	SK-N-SH	brain:	n/a
38	chr2:55281781-55281831	HepG2	liver:	n/a
39	chr2:55239331-55239381	LNCaP	prostate:	n/a
40	chr2:55289112-55289162	T-47D	breast:	n/a
41	chr2:55277876-55277926	HCPEpiC	choroid plexus:	n/a
42	chr2:55239331-55239381	PrEC	prostate:	n/a
43	chr2:55276456-55276506	HAEpiC	amniotic membrane:	n/a
44	chr2:55266232-55266282	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:55276186-55276236	Caco-2	colon:	n/a
46	chr2:55254945-55254995	SAEC	small airway:	n/a
47	chr2:55226987-55227037	IMR90	lung:	fetal
48	chr2:55277876-55277926	HNPCEpiC	eye:	n/a
49	chr2:55239331-55239381	HEEpiC	esophagus:	n/a
50	chr2:55276306-55276356	NHDF-neo	bronchial:	n/a

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr2:55219389..55222736-chr2:55233484..55237490,3	MCF-7	breast:
2	chr2:55252582..55260799-chr2:55274165..55279100,17	MCF-7	breast:
3	chr2:55197790..55202065-chr2:55203128..55206918,7	K562	blood:
4	chr2:55245750..55247978-chr2:55249196..55251041,2	MCF-7	breast:
5	chr2:55276176..55276756-chr7:100209468..100210247,2	Hela-S3	cervix:
6	chr2:55275701..55277282-chr2:55297013..55299339,2	MCF-7	breast:
7	chr2:55239258..55241140-chr2:55243082..55244742,2	K562	blood:
8	chr2:55288774..55290302-chr2:55293407..55295597,2	K562	blood:
9	chr2:55256333..55257873-chr2:55260544..55262457,2	MCF-7	breast:
10	chr2:55275046..55275830-chr2:55395421..55396072,2	MCF-7	breast:
11	chr2:55241176..55242945-chr2:55276344..55278140,2	MCF-7	breast:
12	chr2:55251702..55254676-chr2:55343936..55346646,2	K562	blood:
13	chr2:55238125..55242197-chr2:55249599..55253048,4	K562	blood:
14	chr2:55239250..55241157-chr2:55276968..55279206,2	K562	blood:
15	chr2:55226114..55228646-chr2:55241390..55244484,3	K562	blood:
16	chr2:55290475..55291200-chr2:55402493..55403001,2	MCF-7	breast:
17	chr2:55274620..55276240-chr2:55348004..55351084,3	K562	blood:
18	chr2:55243006..55245333-chr2:55275948..55278441,2	MCF-7	breast:
19	chr2:55251258..55253325-chr2:55261770..55263673,2	K562	blood:
20	chr2:55224031..55227614-chr2:55234894..55236977,3	K562	blood:
21	chr2:55249100..55249700-chr2:55260972..55261897,2	K562	blood:
22	chr2:55261058..55265438-chr2:55268460..55270489,4	MCF-7	breast:
23	chr2:55275729..55276355-chr2:55459417..55460280,3	Hela-S3	cervix:
24	chr2:55276285..55277088-chr20:57466816..57467609,2	Hela-S3	cervix:
25	chr2:55276234..55278687-chr2:55294375..55296735,2	MCF-7	breast:
26	chr2:55240957..55243233-chr2:55273939..55276356,2	K562	blood:
27	chr2:55255325..55257378-chr2:55267721..55270534,4	MCF-7	breast:
28	chr2:55223597..55226125-chr2:55260747..55262677,2	K562	blood:
29	chr2:55245750..55247978-chr2:55249196..55251041,2	MCF-7	breast:
30	chr2:55255745..55260236-chr2:55263069..55266549,5	K562	blood:
31	chr2:55220380..55222677-chr2:55274921..55277767,2	MCF-7	breast:
32	chr2:55255186..55258524-chr2:55346221..55348339,3	K562	blood:
33	chr2:55253298..55255265-chr2:55265294..55267097,2	MCF-7	breast:
34	chr2:55257553..55263983-chr2:55266645..55270936,7	K562	blood:
35	chr2:55306855..55308642-chr2:55313983..55316213,2	K562	blood:
36	chr2:55269242..55271326-chr2:55360631..55363213,2	K562	blood:
37	chr2:55248265..55251849-chr2:55275117..55277756,4	MCF-7	breast:
38	chr2:55257154..55258943-chr2:55260166..55262885,2	K562	blood:
39	chr2:55276798..55279791-chr2:55841794..55843892,2	K562	blood:
40	chr2:55287997..55290069-chr2:55324008..55326423,2	K562	blood:
41	chr2:55247845..55251421-chr2:55399362..55401204,3	K562	blood:
42	chr2:55300544..55302491-chr2:55314911..55316564,2	K562	blood:
43	chr2:55131786..55132384-chr2:55236584..55237394,2	MCF-7	breast:
44	chr17:79479167..79480016-chr2:55276612..55277205,2	Hela-S3	cervix:
45	chr2:55269225..55270745-chr2:55271191..55272770,2	MCF-7	breast:
46	chr2:55137803..55139828-chr2:55230567..55233555,2	K562	blood:
47	chr2:55279956..55282350-chr2:55389384..55392221,3	K562	blood:
48	chr2:55280650..55283253-chr2:55298459..55300307,2	K562	blood:
49	chr2:55275188..55278852-chr2:55297245..55299744,3	MCF-7	breast:
50	chr2:55243166..55246645-chr2:55249862..55254918,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf63-2	chr2:55283619-55283693	NONHSAT070760
2	lnc-C2orf63-2	chr2:55307625-55307775	NONHSAT070760
3	lnc-C2orf63-2	chr2:55287742-55287889	NONHSAT070760

No data

Variant related genes	Relation type
RTN4	TF binding region
RNU6-433P	TF binding region
RTN4	CpG island
RNU6-433P	CpG island
ENSG00000167930	chromatin interactions
ENSG00000200086	chromatin interactions
ENSG00000266376	chromatin interactions
ENSG00000115310	chromatin interactions
ENSG00000203327	chromatin interactions
ENSG00000030582	chromatin interactions
ENSG00000227799	chromatin interactions
ENSG00000264229	chromatin interactions
ENSG00000048471	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000171612	chromatin interactions
ENSG00000151748	chromatin interactions
ENSG00000213358	chromatin interactions
ENSG00000146842	chromatin interactions
ENSG00000085760	chromatin interactions
ENSG00000127957	chromatin interactions
ENSG00000232104	chromatin interactions
ENSG00000087460	chromatin interactions
ENSG00000170634	chromatin interactions
ENSG00000123505	chromatin interactions
ENSG00000106330	chromatin interactions
ENSG00000156671	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000068878	chromatin interactions
ENSG00000214595	chromatin interactions
ENSG00000074054	chromatin interactions
ENSG00000234719	chromatin interactions
ENSG00000088930	chromatin interactions
ENSG00000092853	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000143933	chromatin interactions
ENSG00000143947	chromatin interactions
ENSG00000169814	chromatin interactions
ENSG00000162994	chromatin interactions
ENSG00000131373	chromatin interactions
ENSG00000138041	chromatin interactions
ENSG00000272606	chromatin interactions

Extended variants
information (count: 4312 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4312 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2919125	chr2:55205262-55205263	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142605778	chr2:55205323-55205324	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs547058397	chr2:55205340-55205341	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs552028984	chr2:55205369-55205370	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs181511745	chr2:55205378-55205379	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs565682434	chr2:55205409-55205410	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs527672731	chr2:55205426-55205427	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544257296	chr2:55205427-55205428	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs376572906	chr2:55205435-55205436	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536371556	chr2:55205471-55205472	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs563843872	chr2:55205499-55205500	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs185654669	chr2:55205503-55205504	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs189922011	chr2:55205516-55205517	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs112093980	chr2:55205522-55205523	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs182888296	chr2:55205526-55205527	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs187487550	chr2:55205529-55205530	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs151288793	chr2:55205541-55205542	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs372360859	chr2:55205553-55205554	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs192387278	chr2:55205554-55205555	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs34302889	chr2:55205568-55205569	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs202000601	chr2:55205584-55205585	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs562600128	chr2:55205588-55205589	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs397728989	chr2:55205589-55205590	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs532168885	chr2:55205596-55205597	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs140550689	chr2:55205629-55205630	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs150124871	chr2:55205779-55205780	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs375436138	chr2:55205840-55205841	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs184012678	chr2:55205845-55205846	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs375421277	chr2:55205856-55205857	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs187839930	chr2:55205863-55205864	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs561142694	chr2:55205886-55205887	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs530144355	chr2:55205889-55205890	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs192323160	chr2:55205890-55205891	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs6739210	chr2:55205947-55205948	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs569199668	chr2:55205973-55205974	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs73936512	chr2:55206005-55206006	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552807314	chr2:55206006-55206007	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs551851385	chr2:55206020-55206021	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs566346571	chr2:55206039-55206040	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs371367963	chr2:55206045-55206046	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs550972458	chr2:55206051-55206052	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs76885098	chr2:55206059-55206060	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs369224413	chr2:55206089-55206090	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs551570408	chr2:55206105-55206106	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs138578508	chr2:55206114-55206115	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs539632268	chr2:55206116-55206117	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs574328556	chr2:55206130-55206131	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs141562816	chr2:55206147-55206148	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs145210820	chr2:55206178-55206179	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs576542613	chr2:55206184-55206185	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	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
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4604 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55183200-55206800	Weak transcription	Stomach Mucosa	stomach
2	chr2:55184800-55214800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:55191800-55211600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr2:55191800-55234200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr2:55193400-55214800	Strong transcription	HepG2	liver
6	chr2:55193600-55214600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:55193800-55211800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr2:55194000-55211800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr2:55195000-55215200	Strong transcription	Dnd41	blood
10	chr2:55195200-55205600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:55195200-55205800	Strong transcription	HMEC	breast
12	chr2:55195600-55210800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr2:55195800-55216200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr2:55196000-55205800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:55196200-55214600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:55196200-55226400	Weak transcription	Thymus	Thymus
17	chr2:55196600-55208400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr2:55196600-55217200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:55196600-55217200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:55196800-55205600	Strong transcription	NHEK	skin
21	chr2:55197800-55207800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr2:55198200-55212000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:55198200-55237200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:55198600-55215200	Weak transcription	Lung	lung
25	chr2:55198800-55215200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr2:55199000-55206800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr2:55199200-55206600	Weak transcription	Hela-S3	cervix
28	chr2:55199200-55212400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr2:55199400-55208000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr2:55200200-55209600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr2:55200400-55213400	Weak transcription	Fetal Brain Male	brain
32	chr2:55200800-55208000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr2:55200800-55216600	Weak transcription	Colonic Mucosa	Colon
34	chr2:55201000-55208400	Weak transcription	Placenta	Placenta
35	chr2:55201200-55208000	Weak transcription	Primary B cells from peripheral blood	blood
36	chr2:55201400-55208400	Weak transcription	Primary B cells from cord blood	blood
37	chr2:55202000-55207800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr2:55202400-55205400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:55202600-55205600	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr2:55203400-55205400	Strong transcription	Fetal Muscle Trunk	muscle
41	chr2:55203600-55205400	Strong transcription	A549	lung
42	chr2:55203800-55206200	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr2:55203800-55207800	Weak transcription	Psoas Muscle	Psoas
44	chr2:55203800-55207800	Weak transcription	HUVEC	blood vessel
45	chr2:55203800-55210000	Weak transcription	Ovary	ovary
46	chr2:55203800-55210800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:55203800-55222600	Weak transcription	Spleen	Spleen
48	chr2:55203800-55223800	Weak transcription	Pancreas	Pancrea
49	chr2:55203800-55258400	Weak transcription	Esophagus	oesophagus
50	chr2:55204000-55206200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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