Variant report

Variant	nsv457941
Chromosome Location	chr2:55517491-55585915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:244)
Chromatin interactive
region (count:50)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55569819-55570013	HepG2	liver:	n/a	n/a
2	ATF2	chr2:55538284-55539073	GM12878	blood:	n/a	n/a
3	ATF2	chr2:55538318-55539135	GM12878	blood:	n/a	n/a
4	ATF2	chr2:55523307-55523927	GM12878	blood:	n/a	n/a
5	ATF2	chr2:55529331-55529829	GM12878	blood:	n/a	n/a
6	ATF2	chr2:55529274-55529855	GM12878	blood:	n/a	n/a
7	ATF2	chr2:55523473-55523953	GM12878	blood:	n/a	n/a
8	BATF	chr2:55538437-55539121	GM12878	blood:	n/a	n/a
9	BATF	chr2:55542020-55542394	GM12878	blood:	n/a	chr2:55542211-55542221 chr2:55542210-55542221
10	BATF	chr2:55538455-55539013	GM12878	blood:	n/a	n/a
11	BATF	chr2:55523487-55523919	GM12878	blood:	n/a	n/a
12	BATF	chr2:55529332-55529717	GM12878	blood:	n/a	n/a
13	BATF	chr2:55529422-55529698	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:55538483-55539067	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:55529336-55529669	GM12878	blood:	n/a	chr2:55529597-55529606
16	BCL11A	chr2:55529282-55529766	GM12878	blood:	n/a	chr2:55529597-55529606
17	BCL11A	chr2:55538417-55539027	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:55542063-55542391	GM12878	blood:	n/a	chr2:55542210-55542219
19	BCL11A	chr2:55523450-55523911	GM12878	blood:	n/a	n/a
20	BCL11A	chr2:55523485-55523768	GM12878	blood:	n/a	n/a
21	BCL3	chr2:55538496-55539033	GM12878	blood:	n/a	n/a
22	BCLAF1	chr2:55523368-55523864	GM12878	blood:	n/a	n/a
23	BCLAF1	chr2:55538437-55539096	GM12878	blood:	n/a	n/a
24	BCLAF1	chr2:55538467-55539105	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:55523516-55523858	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:55538500-55539062	GM12878	blood:	n/a	n/a
27	BHLHE40	chr2:55529339-55529771	GM12878	blood:	n/a	n/a
28	CCNT2	chr2:55520341-55520369	K562	blood:	n/a	n/a
29	CEBPB	chr2:55585217-55585405	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:55538642-55538947	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:55566808-55566968	HepG2	liver:	n/a	chr2:55566870-55566887 chr2:55566873-55566884 chr2:55566873-55566886
32	CEBPB	chr2:55538706-55539014	A549	lung:	n/a	n/a
33	CEBPB	chr2:55538685-55538968	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr2:55561933-55562146	HepG2	liver:	n/a	chr2:55562048-55562059
35	CEBPB	chr2:55573211-55573321	K562	blood:	n/a	chr2:55573295-55573308 chr2:55573295-55573308 chr2:55573295-55573306
36	CEBPB	chr2:55558502-55558529	K562	blood:	n/a	chr2:55558515-55558526 chr2:55558513-55558526
37	CEBPB	chr2:55529242-55529998	GM12878	blood:	n/a	n/a
38	CEBPB	chr2:55523381-55523980	GM12878	blood:	n/a	n/a
39	CEBPB	chr2:55565470-55565825	IMR90	lung:	n/a	chr2:55565642-55565655
40	CEBPB	chr2:55561949-55562177	K562	blood:	n/a	chr2:55562048-55562059
41	CEBPB	chr2:55566840-55566848	A549	lung:	n/a	n/a
42	CEBPB	chr2:55538323-55539139	GM12878	blood:	n/a	n/a
43	CEBPB	chr2:55566840-55566910	K562	blood:	n/a	chr2:55566870-55566887 chr2:55566873-55566884 chr2:55566873-55566886
44	CHD2	chr2:55523526-55523672	GM12878	blood:	n/a	n/a
45	CREB1	chr2:55538359-55539061	GM12878	blood:	n/a	n/a
46	CREB1	chr2:55529321-55529897	GM12878	blood:	n/a	n/a
47	CREB1	chr2:55529336-55529766	GM12878	blood:	n/a	n/a
48	CTCF	chr2:55538820-55538970	Caco-2	colon:	n/a	n/a
49	CTCF	chr2:55541140-55541290	HepG2	liver:	n/a	n/a
50	CTCF	chr2:55538780-55538930	NB4	blood:	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	chr2:55556195-55556245	SKMC	muscle:	n/a
2	chr2:55556195-55556245	ECC-1	luminal epithelium:	n/a
3	chr2:55563533-55563583	A549	lung:	n/a
4	chr2:55556195-55556245	GM12892	blood:	n/a
5	chr2:55566679-55566729	IMR90	lung:	fetal
6	chr2:55556201-55556251	NH-A	brain:	n/a
7	chr2:55563533-55563583	Hela-S3	cervix:	n/a
8	chr2:55556201-55556251	GM06990	blood:	n/a
9	chr2:55566679-55566729	T-47D	breast:	n/a
10	chr2:55566679-55566729	HIPEpiC	eye:	n/a
11	chr2:55563533-55563583	Caco-2	colon:	n/a
12	chr2:55556201-55556251	NB4	blood:	n/a
13	chr2:55556195-55556245	NH-A	brain:	n/a
14	chr2:55556201-55556251	AoSMC	blood vessel:	n/a
15	chr2:55556195-55556245	Hepatocyte	liver:	n/a
16	chr2:55566679-55566729	HCT-116	colon:	n/a
17	chr2:55566679-55566729	PrEC	prostate:	n/a
18	chr2:55566679-55566729	PFSK-1	brain:	n/a
19	chr2:55563533-55563583	MCF-7	breast:	n/a
20	chr2:55566679-55566729	AG04450	lung:	fetal
21	chr2:55566679-55566729	NT2-D1	testis:	n/a
22	chr2:55566679-55566729	K562	blood:	n/a
23	chr2:55556201-55556251	ovcar-3	ovarian:	n/a
24	chr2:55556201-55556251	Hepatocyte	liver:	n/a
25	chr2:55556201-55556251	Jurkat	blood:	n/a
26	chr2:55556195-55556245	AG04450	lung:	fetal
27	chr2:55556195-55556245	HRPEpiC	eye:	n/a
28	chr2:55556195-55556245	HNPCEpiC	eye:	n/a
29	chr2:55566679-55566729	RPTEC	kidney:	n/a
30	chr2:55556195-55556245	GM19239	blood:	n/a
31	chr2:55563533-55563583	NB4	blood:	n/a
32	chr2:55566679-55566729	ProgFib	skin:	n/a
33	chr2:55556195-55556245	SK-N-SH	brain:	n/a
34	chr2:55556201-55556251	HPAEpiC	pulmonary alveolar:	n/a
35	chr2:55556195-55556245	NT2-D1	testis:	n/a
36	chr2:55556195-55556245	HEEpiC	esophagus:	n/a
37	chr2:55556201-55556251	HRPEpiC	eye:	n/a
38	chr2:55556201-55556251	NHDF-neo	bronchial:	n/a
39	chr2:55556195-55556245	Hela-S3	cervix:	n/a
40	chr2:55556195-55556245	AG04449	skin:	fetal
41	chr2:55563533-55563583	CMK	blood:	n/a
42	chr2:55566679-55566729	AG09319	gingival:	n/a
43	chr2:55563533-55563583	K562	blood:	n/a
44	chr2:55556201-55556251	HCF	heart:	n/a
45	chr2:55556201-55556251	HNPCEpiC	eye:	n/a
46	chr2:55556201-55556251	PrEC	prostate:	n/a
47	chr2:55563533-55563583	AG04450	lung:	fetal
48	chr2:55566679-55566729	CMK	blood:	n/a
49	chr2:55566679-55566729	HL-60	blood:	n/a
50	chr2:55563533-55563583	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:55510957..55512657-chr2:55520415..55521941,2	MCF-7	breast:
2	chr2:55545501..55548363-chr2:55552487..55555992,3	K562	blood:
3	chr2:55579484..55581776-chr2:55584319..55586422,2	K562	blood:
4	chr2:55514301..55516151-chr2:55518959..55520928,3	MCF-7	breast:
5	chr2:55555173..55557100-chr2:55560073..55561601,2	K562	blood:
6	chr2:55540921..55542713-chr2:55544726..55547576,2	MCF-7	breast:
7	chr2:55521570..55523251-chr2:55525570..55527092,2	MCF-7	breast:
8	chr2:55555173..55557100-chr2:55560073..55561601,2	K562	blood:
9	chr2:55540693..55542535-chr2:55543595..55545823,2	K562	blood:
10	chr2:55509212..55512081-chr2:55556525..55559325,2	MCF-7	breast:
11	chr2:55517531..55519068-chr2:55523898..55526477,2	MCF-7	breast:
12	chr2:55516061..55518491-chr2:55518529..55520349,2	K562	blood:
13	chr2:55520326..55522931-chr2:55543015..55545040,2	K562	blood:
14	chr2:55516323..55518543-chr2:55519705..55522425,2	MCF-7	breast:
15	chr2:55550452..55552052-chr2:55563952..55565660,2	MCF-7	breast:
16	chr2:55579484..55581776-chr2:55584319..55586422,2	K562	blood:
17	chr2:55518930..55520910-chr2:55525941..55528054,2	K562	blood:
18	chr2:55553356..55555792-chr2:55563931..55566762,2	K562	blood:
19	chr2:55516061..55518491-chr2:55518529..55520349,2	K562	blood:
20	chr2:55579484..55583558-chr2:55584922..55587594,3	K562	blood:
21	chr2:55567779..55569483-chr2:55585601..55588441,2	MCF-7	breast:
22	chr2:55579484..55583558-chr2:55584922..55587594,3	K562	blood:
23	chr2:55495242..55497992-chr2:55516142..55518443,2	K562	blood:
24	chr2:55545711..55548722-chr2:55552487..55555212,4	K562	blood:
25	chr2:55517623..55519304-chr2:55522229..55524562,2	K562	blood:
26	chr2:55513717..55517670-chr2:55518024..55521740,6	K562	blood:
27	chr2:55554925..55556673-chr2:55560073..55562213,2	K562	blood:
28	chr2:55513717..55517670-chr2:55518024..55521740,6	K562	blood:
29	chr2:55567779..55569483-chr2:55585601..55588441,2	MCF-7	breast:
30	chr2:55528159..55530005-chr2:55532153..55533845,2	MCF-7	breast:
31	chr2:55494684..55499569-chr2:55516943..55523168,5	K562	blood:
32	chr2:55540693..55542535-chr2:55543595..55545823,2	K562	blood:
33	chr2:55512725..55515035-chr2:55515151..55518093,2	MCF-7	breast:
34	chr2:55545183..55549012-chr2:55745098..55746778,3	MCF-7	breast:
35	chr2:55545711..55548722-chr2:55552487..55555212,4	K562	blood:
36	chr2:55540921..55542713-chr2:55544726..55547576,2	MCF-7	breast:
37	chr2:55517531..55519068-chr2:55523898..55526477,2	MCF-7	breast:
38	chr2:55516323..55518543-chr2:55519705..55522425,2	MCF-7	breast:
39	chr2:55546328..55548637-chr2:55556115..55557896,2	K562	blood:
40	chr2:55521570..55523251-chr2:55525570..55527092,2	MCF-7	breast:
41	chr2:55550452..55552052-chr2:55563952..55565660,2	MCF-7	breast:
42	chr2:55584108..55586165-chr2:55591531..55593375,2	K562	blood:
43	chr2:55517623..55519304-chr2:55522229..55524562,2	K562	blood:
44	chr2:55570093..55571972-chr2:55587892..55590606,2	K562	blood:
45	chr2:55518930..55520910-chr2:55525941..55528054,2	K562	blood:
46	chr2:55536648..55539597-chr2:55541310..55544144,3	K562	blood:
47	chr2:55528159..55530005-chr2:55532153..55533845,2	MCF-7	breast:
48	chr2:55546328..55548637-chr2:55556115..55557896,2	K562	blood:
49	chr2:55543117..55545665-chr2:55550405..55552133,2	K562	blood:
50	chr2:55554925..55556673-chr2:55560073..55562213,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPS27A-1	chr2:55541218-55541387	ENSG00000240401.4
2	lnc-RPS27A-1	chr2:55572493-55573185	ENSG00000240401.4
3	lnc-RPS27A-1	chr2:55556558-55556849	ENSG00000240401.4
4	lnc-RPS27A-1	chr2:55541124-55541797	ENSG00000240401.4
5	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4
6	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4
7	lnc-RPS27A-1	chr2:55535628-55536063	ENSG00000240401.4
8	lnc-RPS27A-1	chr2:55541124-55541797	ENSG00000240401.2
9	lnc-RPS27A-1	chr2:55535967-55536063	ENSG00000240401.2
10	lnc-RPS27A-1	chr2:55566639-55566931	ENSG00000240401.4
11	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4
12	lnc-RPS27A-1	chr2:55556558-55556655	ENSG00000240401.4
13	lnc-RPS27A-1	chr2:55566639-55567304	ENSG00000240401.4
14	lnc-RPS27A-1	chr2:55566639-55567446	ENSG00000240401.4

No data

Variant related genes	Relation type
ENSG00000240401	TF binding region
CCDC88A	TF binding region
ENSG00000240401	CpG island
CCDC88A	CpG island
ENSG00000240401	chromatin interactions
ENSG00000115355	chromatin interactions
ENSG00000162997	chromatin interactions
ENSG00000163001	chromatin interactions
ENSG00000206964	chromatin interactions
ENSG00000085760	chromatin interactions

Extended variants
information (count: 2673 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2673 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1047948	chr2:55517491-55517492	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144826545	chr2:55517493-55517494	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs1047946	chr2:55517513-55517514	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs146721738	chr2:55517586-55517587	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534488178	chr2:55517629-55517630	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188767121	chr2:55517677-55517678	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs574357755	chr2:55517685-55517686	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs11888119	chr2:55517699-55517700	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs556478467	chr2:55517935-55517936	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs560457854	chr2:55517938-55517939	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs576346291	chr2:55517999-55518000	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs545528225	chr2:55518005-55518006	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs565221397	chr2:55518008-55518009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs527906331	chr2:55518082-55518083	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs376353944	chr2:55518102-55518103	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541612461	chr2:55518109-55518110	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529227696	chr2:55518155-55518156	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549001479	chr2:55518164-55518165	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs192870686	chr2:55518228-55518229	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569251340	chr2:55518230-55518231	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550486647	chr2:55518250-55518251	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs369394776	chr2:55518263-55518264	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs569680303	chr2:55518273-55518274	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185136033	chr2:55518308-55518309	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372034540	chr2:55518325-55518326	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553566206	chr2:55518333-55518334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188060610	chr2:55518361-55518362	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565603542	chr2:55518376-55518377	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs202037388	chr2:55518378-55518379	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534529827	chr2:55518386-55518387	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191480306	chr2:55518394-55518395	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs568021493	chr2:55518415-55518416	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536986520	chr2:55518473-55518474	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs556969992	chr2:55518504-55518505	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561438543	chr2:55518518-55518519	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs576419893	chr2:55518540-55518541	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531785389	chr2:55518554-55518555	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs183641260	chr2:55518563-55518564	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148959590	chr2:55518644-55518645	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs115015859	chr2:55518687-55518688	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs541654937	chr2:55518710-55518711	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551856935	chr2:55518738-55518739	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2249856	chr2:55518742-55518743	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs530313960	chr2:55518759-55518760	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35746882	chr2:55518821-55518822	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375867449	chr2:55518824-55518825	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs377524973	chr2:55518830-55518831	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs200026991	chr2:55518851-55518852	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs200404307	chr2:55518858-55518859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375482415	chr2:55518880-55518881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 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
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	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	chr2:55509000-55541200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:55509400-55545200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr2:55509600-55522600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:55509800-55518600	Weak transcription	HMEC	breast
5	chr2:55509800-55521800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:55510000-55518800	Weak transcription	Brain Angular Gyrus	brain
7	chr2:55510000-55521600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:55510000-55521600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr2:55510000-55521800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:55510000-55521800	Weak transcription	Fetal Brain Male	brain
11	chr2:55510000-55521800	Weak transcription	NHEK	skin
12	chr2:55510000-55522000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr2:55510000-55522200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr2:55510000-55522200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:55510000-55522400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr2:55510000-55522400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr2:55510000-55522600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr2:55510000-55541600	Weak transcription	Esophagus	oesophagus
19	chr2:55510000-55553600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr2:55510000-55578800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:55510200-55519200	Weak transcription	Ovary	ovary
22	chr2:55510200-55520600	Weak transcription	HSMMtube	muscle
23	chr2:55510200-55521800	Weak transcription	Fetal Kidney	kidney
24	chr2:55510200-55522200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr2:55510200-55522400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr2:55510200-55522400	Weak transcription	NHLF	lung
27	chr2:55510200-55522600	Weak transcription	Aorta	Aorta
28	chr2:55510200-55542200	Weak transcription	Fetal Intestine Large	intestine
29	chr2:55510200-55559000	Weak transcription	Psoas Muscle	Psoas
30	chr2:55510200-55616800	Weak transcription	Fetal Intestine Small	intestine
31	chr2:55510400-55522400	Weak transcription	Left Ventricle	heart
32	chr2:55510400-55529000	Weak transcription	Placenta	Placenta
33	chr2:55510600-55519400	Weak transcription	Primary B cells from cord blood	blood
34	chr2:55510600-55521800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:55510600-55522400	Weak transcription	A549	lung
36	chr2:55510600-55533800	Weak transcription	Pancreas	Pancrea
37	chr2:55510600-55536600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr2:55510600-55537400	Weak transcription	Lung	lung
39	chr2:55510800-55518200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr2:55510800-55518600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr2:55510800-55521200	Weak transcription	Osteobl	bone
42	chr2:55510800-55521800	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr2:55510800-55542200	Weak transcription	Rectal Smooth Muscle	rectum
44	chr2:55511000-55518800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr2:55511000-55519600	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr2:55511000-55521600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr2:55511000-55521800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr2:55511000-55521800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr2:55511000-55540600	Weak transcription	Spleen	Spleen
50	chr2:55511200-55519400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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