Variant report

Variant	nsv874159
Chromosome Location	chr2:55513738-55636351
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:703)
CpG islands
(count:366)
Chromatin interactive
region (count:88)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55618268-55619692	K562	blood:	n/a	n/a
2	ARID3A	chr2:55592432-55592822	K562	blood:	n/a	n/a
3	ARID3A	chr2:55569819-55570013	HepG2	liver:	n/a	n/a
4	ATF1	chr2:55592548-55592774	K562	blood:	n/a	n/a
5	ATF2	chr2:55523307-55523927	GM12878	blood:	n/a	n/a
6	ATF2	chr2:55529274-55529855	GM12878	blood:	n/a	n/a
7	ATF2	chr2:55538318-55539135	GM12878	blood:	n/a	n/a
8	ATF2	chr2:55529331-55529829	GM12878	blood:	n/a	n/a
9	ATF2	chr2:55523473-55523953	GM12878	blood:	n/a	n/a
10	ATF2	chr2:55538284-55539073	GM12878	blood:	n/a	n/a
11	BATF	chr2:55523487-55523919	GM12878	blood:	n/a	n/a
12	BATF	chr2:55542020-55542394	GM12878	blood:	n/a	chr2:55542211-55542221 chr2:55542210-55542221
13	BATF	chr2:55529422-55529698	GM12878	blood:	n/a	n/a
14	BATF	chr2:55538455-55539013	GM12878	blood:	n/a	n/a
15	BATF	chr2:55538437-55539121	GM12878	blood:	n/a	n/a
16	BATF	chr2:55529332-55529717	GM12878	blood:	n/a	n/a
17	BATF	chr2:55623002-55623354	GM12878	blood:	n/a	n/a
18	BCL11A	chr2:55529282-55529766	GM12878	blood:	n/a	chr2:55529597-55529606
19	BCL11A	chr2:55542063-55542391	GM12878	blood:	n/a	chr2:55542210-55542219
20	BCL11A	chr2:55529336-55529669	GM12878	blood:	n/a	chr2:55529597-55529606
21	BCL11A	chr2:55523485-55523768	GM12878	blood:	n/a	n/a
22	BCL11A	chr2:55538417-55539027	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:55523450-55523911	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:55538483-55539067	GM12878	blood:	n/a	n/a
25	BCL3	chr2:55538496-55539033	GM12878	blood:	n/a	n/a
26	BCLAF1	chr2:55538437-55539096	GM12878	blood:	n/a	n/a
27	BCLAF1	chr2:55538467-55539105	GM12878	blood:	n/a	n/a
28	BCLAF1	chr2:55523368-55523864	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:55618324-55618481	K562	blood:	n/a	n/a
30	BHLHE40	chr2:55538500-55539062	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:55619300-55619302	K562	blood:	n/a	n/a
32	BHLHE40	chr2:55618108-55618117	K562	blood:	n/a	n/a
33	BHLHE40	chr2:55523516-55523858	GM12878	blood:	n/a	n/a
34	BHLHE40	chr2:55622905-55623263	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:55529339-55529771	GM12878	blood:	n/a	n/a
36	CBX3	chr2:55618040-55619310	K562	blood:	n/a	n/a
37	CCNT2	chr2:55619504-55619632	K562	blood:	n/a	n/a
38	CCNT2	chr2:55609176-55609272	K562	blood:	n/a	n/a
39	CCNT2	chr2:55520341-55520369	K562	blood:	n/a	n/a
40	CCNT2	chr2:55618269-55618444	K562	blood:	n/a	n/a
41	CEBPB	chr2:55591272-55591757	Hela-S3	cervix:	n/a	chr2:55591616-55591629
42	CEBPB	chr2:55591247-55591771	IMR90	lung:	n/a	chr2:55591616-55591629
43	CEBPB	chr2:55598162-55598340	K562	blood:	n/a	chr2:55598260-55598273
44	CEBPB	chr2:55585217-55585405	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:55593589-55593662	K562	blood:	n/a	n/a
46	CEBPB	chr2:55611975-55612307	A549	lung:	n/a	chr2:55612124-55612135 chr2:55612126-55612135
47	CEBPB	chr2:55538685-55538968	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:55523381-55523980	GM12878	blood:	n/a	n/a
49	CEBPB	chr2:55630386-55630675	HepG2	liver:	n/a	chr2:55630545-55630556
50	CEBPB	chr2:55630444-55630590	K562	blood:	n/a	chr2:55630545-55630556

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55556201-55556251	BE2_C	brain:	n/a
2	chr2:55556201-55556251	Jurkat	blood:	n/a
3	chr2:55563533-55563583	LNCaP	prostate:	n/a
4	chr2:55566679-55566729	BE2_C	brain:	n/a
5	chr2:55556195-55556245	AG04450	lung:	fetal
6	chr2:55566679-55566729	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:55566679-55566729	NT2-D1	testis:	n/a
8	chr2:55556201-55556251	SAEC	small airway:	n/a
9	chr2:55515029-55515079	SAEC	small airway:	n/a
10	chr2:55563533-55563583	HepG2	liver:	n/a
11	chr2:55563533-55563583	CMK	blood:	n/a
12	chr2:55556195-55556245	U87	brain:	n/a
13	chr2:55566679-55566729	A549	lung:	n/a
14	chr2:55563533-55563583	AG09309	skin:	n/a
15	chr2:55556195-55556245	NB4	blood:	n/a
16	chr2:55556201-55556251	HRPEpiC	eye:	n/a
17	chr2:55566679-55566729	HEK293	kidney:	embryo
18	chr2:55515029-55515079	ECC-1	luminal epithelium:	n/a
19	chr2:55566679-55566729	AG09309	skin:	n/a
20	chr2:55563533-55563583	HNPCEpiC	eye:	n/a
21	chr2:55556201-55556251	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:55556201-55556251	Hepatocyte	liver:	n/a
23	chr2:55566679-55566729	AG04449	skin:	fetal
24	chr2:55556201-55556251	U87	brain:	n/a
25	chr2:55556195-55556245	LNCaP	prostate:	n/a
26	chr2:55566679-55566729	GM12891	blood:	n/a
27	chr2:55556195-55556245	HNPCEpiC	eye:	n/a
28	chr2:55515029-55515079	Jurkat	blood:	n/a
29	chr2:55566679-55566729	AG04450	lung:	fetal
30	chr2:55556195-55556245	ProgFib	skin:	n/a
31	chr2:55566679-55566729	NB4	blood:	n/a
32	chr2:55556195-55556245	AG10803	skin:	n/a
33	chr2:55556201-55556251	NHDF-neo	bronchial:	n/a
34	chr2:55515029-55515079	PrEC	prostate:	n/a
35	chr2:55563533-55563583	AG10803	skin:	n/a
36	chr2:55617438-55617488	AG04449	skin:	fetal
37	chr2:55566679-55566729	SK-N-MC	brain:	n/a
38	chr2:55556201-55556251	AoSMC	blood vessel:	n/a
39	chr2:55515029-55515079	HMEC	breast:	n/a
40	chr2:55515029-55515079	HCF	heart:	n/a
41	chr2:55556201-55556251	NB4	blood:	n/a
42	chr2:55617438-55617488	Hela-S3	cervix:	n/a
43	chr2:55617438-55617488	HAEpiC	amniotic membrane:	n/a
44	chr2:55566679-55566729	GM12878	blood:	n/a
45	chr2:55617438-55617488	HEEpiC	esophagus:	n/a
46	chr2:55515029-55515079	HRPEpiC	eye:	n/a
47	chr2:55617438-55617488	GM12878	blood:	n/a
48	chr2:55515029-55515079	IMR90	lung:	fetal
49	chr2:55563533-55563583	HEK293	kidney:	embryo
50	chr2:55515029-55515079	HPAEpiC	pulmonary alveolar:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:212458271..212459805-chr2:55589892..55591748,2	K562	blood:
2	chr2:55509212..55512081-chr2:55556525..55559325,2	MCF-7	breast:
3	chr2:55584108..55586165-chr2:55591531..55593375,2	K562	blood:
4	chr2:55629328..55632200-chr2:55634808..55637417,2	K562	blood:
5	chr2:55509373..55510992-chr2:55512785..55514521,3	MCF-7	breast:
6	chr2:55599888..55601639-chr2:55606569..55609062,2	K562	blood:
7	chr2:55627632..55629326-chr2:55632488..55634437,2	K562	blood:
8	chr2:55545711..55548722-chr2:55552487..55555212,4	K562	blood:
9	chr2:55521570..55523251-chr2:55525570..55527092,2	MCF-7	breast:
10	chr2:55418148..55421092-chr2:55618955..55620570,2	K562	blood:
11	chr2:55546328..55548637-chr2:55556115..55557896,2	K562	blood:
12	chr2:55521570..55523251-chr2:55525570..55527092,2	MCF-7	breast:
13	chr2:55635517..55637604-chr2:55646032..55648354,3	K562	blood:
14	chr2:55514301..55516151-chr2:55518959..55520928,3	MCF-7	breast:
15	chr2:55518930..55520910-chr2:55525941..55528054,2	K562	blood:
16	chr2:55615003..55618126-chr2:55622970..55626824,3	K562	blood:
17	chr2:55627338..55628874-chr2:55629453..55631312,2	MCF-7	breast:
18	chr2:55617949..55620712-chr2:55634436..55637353,2	K562	blood:
19	chr2:55513717..55517670-chr2:55518024..55521740,6	K562	blood:
20	chr2:55495242..55497992-chr2:55516142..55518443,2	K562	blood:
21	chr2:55517531..55519068-chr2:55523898..55526477,2	MCF-7	breast:
22	chr2:55589556..55591958-chr2:55592375..55594974,2	MCF-7	breast:
23	chr2:55550452..55552052-chr2:55563952..55565660,2	MCF-7	breast:
24	chr2:55618745..55621738-chr2:55622062..55625126,3	K562	blood:
25	chr2:55592018..55593531-chr2:55595519..55597043,2	K562	blood:
26	chr2:55586524..55588974-chr2:55589647..55593883,3	K562	blood:
27	chr2:55536648..55539597-chr2:55541310..55544144,3	K562	blood:
28	chr2:55617017..55619738-chr2:55645047..55647887,2	K562	blood:
29	chr2:55615003..55618126-chr2:55622970..55626824,3	K562	blood:
30	chr2:55555173..55557100-chr2:55560073..55561601,2	K562	blood:
31	chr2:55570093..55571972-chr2:55587892..55590606,2	K562	blood:
32	chr2:55554925..55556673-chr2:55560073..55562213,2	K562	blood:
33	chr2:55624788..55628704-chr2:55629085..55632054,3	K562	blood:
34	chr2:55617949..55620712-chr2:55634436..55637353,2	K562	blood:
35	chr2:55516323..55518543-chr2:55519705..55522425,2	MCF-7	breast:
36	chr2:55550452..55552052-chr2:55563952..55565660,2	MCF-7	breast:
37	chr2:55494684..55499569-chr2:55516943..55523168,5	K562	blood:
38	chr2:55618238..55620708-chr2:55645047..55647010,2	K562	blood:
39	chr2:55567779..55569483-chr2:55585601..55588441,2	MCF-7	breast:
40	chr2:55543117..55545665-chr2:55550405..55552133,2	K562	blood:
41	chr2:55528159..55530005-chr2:55532153..55533845,2	MCF-7	breast:
42	chr2:55618745..55621738-chr2:55622062..55625126,3	K562	blood:
43	chr2:55597784..55600046-chr2:55608046..55611475,3	K562	blood:
44	chr2:55570093..55571972-chr2:55587892..55590606,2	K562	blood:
45	chr2:55627632..55629326-chr2:55632488..55634437,2	K562	blood:
46	chr2:55514301..55516151-chr2:55518959..55520928,3	MCF-7	breast:
47	chr2:55517623..55519304-chr2:55522229..55524562,2	K562	blood:
48	chr2:55516061..55518491-chr2:55518529..55520349,2	K562	blood:
49	chr2:55540693..55542535-chr2:55543595..55545823,2	K562	blood:
50	chr2:55545711..55548722-chr2:55552487..55555212,4	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4
2	lnc-MTIF2-4	chr2:55628085-55628362	expReg_chr2_4282_-
3	lnc-RPS27A-1	chr2:55572493-55573185	ENSG00000240401.4
4	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4
5	lnc-RPS27A-1	chr2:55556558-55556655	ENSG00000240401.4
6	lnc-RPS27A-1	chr2:55566639-55566931	ENSG00000240401.4
7	lnc-RPS27A-1	chr2:55535967-55536063	ENSG00000240401.2
8	lnc-RPS27A-1	chr2:55541218-55541387	ENSG00000240401.4
9	lnc-RPS27A-1	chr2:55566639-55567446	ENSG00000240401.4
10	lnc-RPS27A-1	chr2:55535628-55536063	ENSG00000240401.4
11	lnc-RPS27A-1	chr2:55541124-55541797	ENSG00000240401.2
12	lnc-RPS27A-1	chr2:55566639-55567304	ENSG00000240401.4
13	lnc-RPS27A-1	chr2:55556558-55556849	ENSG00000240401.4
14	lnc-RPS27A-1	chr2:55541124-55541797	ENSG00000240401.4
15	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4

No data

Variant related genes	Relation type
ENSG00000240401	TF binding region
CCDC88A	TF binding region
ENSG00000240401	CpG island
CCDC88A	CpG island
ENSG00000163001	chromatin interactions
ENSG00000162997	chromatin interactions
ENSG00000115355	chromatin interactions
ENSG00000066027	chromatin interactions
ENSG00000085760	chromatin interactions
ENSG00000206964	chromatin interactions
ENSG00000240401	chromatin interactions

Extended variants
information (count: 4928 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:4928 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6738970	chr2:55513738-55513739	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557200884	chr2:55513742-55513743	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs184654663	chr2:55513765-55513766	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200697430	chr2:55513822-55513823	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537429217	chr2:55513824-55513825	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs397842057	chr2:55513839-55513840	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs6739348	chr2:55513871-55513872	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs577241347	chr2:55513907-55513908	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs546135158	chr2:55513914-55513915	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553242205	chr2:55513924-55513925	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs189584319	chr2:55513925-55513926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs542155187	chr2:55513946-55513947	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562026855	chr2:55513949-55513950	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs574921282	chr2:55513975-55513976	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs71414559	chr2:55513983-55513984	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs180890883	chr2:55514005-55514006	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs552512626	chr2:55514021-55514022	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs564222252	chr2:55514032-55514033	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs143257263	chr2:55514054-55514055	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs546777228	chr2:55514056-55514057	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560135399	chr2:55514073-55514074	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529091471	chr2:55514087-55514088	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs549333974	chr2:55514099-55514100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs569153734	chr2:55514115-55514116	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537466206	chr2:55514120-55514121	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs550668091	chr2:55514186-55514187	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570936206	chr2:55514280-55514281	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs539592743	chr2:55514313-55514314	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs553419323	chr2:55514320-55514321	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573389883	chr2:55514322-55514323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs535629987	chr2:55514344-55514345	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565495755	chr2:55514508-55514509	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183516317	chr2:55514510-55514511	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs59695161	chr2:55514545-55514546	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs543813786	chr2:55514568-55514569	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189325647	chr2:55514573-55514574	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577563760	chr2:55514581-55514582	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539995972	chr2:55514594-55514595	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78910072	chr2:55514637-55514638	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs11899921	chr2:55514668-55514669	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs561808572	chr2:55514749-55514750	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529132133	chr2:55514832-55514833	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148645271	chr2:55514863-55514864	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372691104	chr2:55514901-55514902	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571624965	chr2:55514924-55514925	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs562788954	chr2:55514953-55514954	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs531599312	chr2:55514984-55514985	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551648223	chr2:55514989-55514990	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570794782	chr2:55514996-55514997	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs12621338	chr2:55515001-55515002	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Melanoma	20877625	CNVD

Chromatin state (count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55501000-55517000	Weak transcription	Hela-S3	cervix
2	chr2:55509000-55541200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:55509400-55515600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:55509400-55545200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr2:55509600-55522600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:55509800-55514600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr2:55509800-55518600	Weak transcription	HMEC	breast
8	chr2:55509800-55521800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:55510000-55514400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:55510000-55515400	Weak transcription	Brain Substantia Nigra	brain
11	chr2:55510000-55516200	Weak transcription	Fetal Lung	lung
12	chr2:55510000-55518800	Weak transcription	Brain Angular Gyrus	brain
13	chr2:55510000-55521600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:55510000-55521600	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:55510000-55521800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:55510000-55521800	Weak transcription	Fetal Brain Male	brain
17	chr2:55510000-55521800	Weak transcription	NHEK	skin
18	chr2:55510000-55522000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr2:55510000-55522200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:55510000-55522200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr2:55510000-55522400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr2:55510000-55522400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr2:55510000-55522600	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr2:55510000-55541600	Weak transcription	Esophagus	oesophagus
25	chr2:55510000-55553600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr2:55510000-55578800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:55510200-55514600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr2:55510200-55516000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:55510200-55516200	Weak transcription	NHDF-Ad	bronchial
30	chr2:55510200-55516600	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr2:55510200-55517400	Weak transcription	Fetal Brain Female	brain
32	chr2:55510200-55519200	Weak transcription	Ovary	ovary
33	chr2:55510200-55520600	Weak transcription	HSMMtube	muscle
34	chr2:55510200-55521800	Weak transcription	Fetal Kidney	kidney
35	chr2:55510200-55522200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr2:55510200-55522400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr2:55510200-55522400	Weak transcription	NHLF	lung
38	chr2:55510200-55522600	Weak transcription	Aorta	Aorta
39	chr2:55510200-55542200	Weak transcription	Fetal Intestine Large	intestine
40	chr2:55510200-55559000	Weak transcription	Psoas Muscle	Psoas
41	chr2:55510200-55616800	Weak transcription	Fetal Intestine Small	intestine
42	chr2:55510400-55515200	Weak transcription	HUVEC	blood vessel
43	chr2:55510400-55515600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr2:55510400-55522400	Weak transcription	Left Ventricle	heart
45	chr2:55510400-55529000	Weak transcription	Placenta	Placenta
46	chr2:55510600-55514400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr2:55510600-55514800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr2:55510600-55519400	Weak transcription	Primary B cells from cord blood	blood
49	chr2:55510600-55521800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:55510600-55522400	Weak transcription	A549	lung

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