Variant report

Variant	nsv873643
Chromosome Location	chr2:10535481-10583160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2409)
CpG islands
(count:1958)
Chromatin interactive
region (count:203)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2409 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:10541695-10541878	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:10549012-10549595	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:10541271-10541473	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:10575114-10575331	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:10575097-10575358	K562	blood:	n/a	n/a
6	ARID3A	chr2:10548446-10549527	K562	blood:	n/a	n/a
7	ATF1	chr2:10552555-10552827	K562	blood:	n/a	n/a
8	ATF1	chr2:10548047-10548815	K562	blood:	n/a	n/a
9	ATF2	chr2:10549110-10549576	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:10550211-10550913	GM12878	blood:	n/a	n/a
11	ATF2	chr2:10550334-10550899	GM12878	blood:	n/a	n/a
12	ATF3	chr2:10552577-10552858	K562	blood:	n/a	n/a
13	ATF3	chr2:10548276-10548838	K562	blood:	n/a	n/a
14	ATF3	chr2:10547847-10548937	A549	lung:	n/a	n/a
15	ATF3	chr2:10552580-10552789	K562	blood:	n/a	n/a
16	ATF3	chr2:10552564-10552899	GM12878	blood:	n/a	n/a
17	ATF3	chr2:10545373-10546017	A549	lung:	n/a	n/a
18	ATF3	chr2:10552620-10552791	GM12878	blood:	n/a	n/a
19	ATF3	chr2:10574995-10575468	A549	lung:	n/a	n/a
20	ATF3	chr2:10549230-10549413	K562	blood:	n/a	n/a
21	ATF3	chr2:10552463-10552936	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr2:10547899-10549667	A549	lung:	n/a	n/a
23	ATF3	chr2:10545380-10546068	A549	lung:	n/a	n/a
24	BACH1	chr2:10549223-10549515	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr2:10549157-10549489	K562	blood:	n/a	n/a
26	BACH1	chr2:10573220-10573459	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr2:10548502-10548944	K562	blood:	n/a	n/a
28	BATF	chr2:10554084-10554479	GM12878	blood:	n/a	n/a
29	BATF	chr2:10550302-10550845	GM12878	blood:	n/a	chr2:10550648-10550658
30	BATF	chr2:10548477-10548791	GM12878	blood:	n/a	chr2:10548672-10548683 chr2:10548673-10548683
31	BATF	chr2:10550479-10550817	GM12878	blood:	n/a	chr2:10550648-10550658
32	BATF	chr2:10554094-10554393	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:10550342-10550816	GM12878	blood:	n/a	chr2:10550647-10550656
34	BCL3	chr2:10574943-10575469	A549	lung:	n/a	n/a
35	BCL3	chr2:10578643-10580663	K562	blood:	n/a	n/a
36	BCL3	chr2:10573217-10573924	GM12878	blood:	n/a	n/a
37	BCL3	chr2:10578813-10579766	GM12878	blood:	n/a	n/a
38	BCL3	chr2:10547742-10549547	A549	lung:	n/a	chr2:10549419-10549427 chr2:10549501-10549514 chr2:10548264-10548273
39	BCL3	chr2:10542212-10542849	A549	lung:	n/a	n/a
40	BCL3	chr2:10578877-10579530	A549	lung:	n/a	n/a
41	BCL3	chr2:10579414-10579981	K562	blood:	n/a	n/a
42	BCL3	chr2:10547533-10548926	A549	lung:	n/a	chr2:10548264-10548273
43	BCL3	chr2:10573234-10573899	GM12878	blood:	n/a	n/a
44	BCL3	chr2:10545367-10546374	A549	lung:	n/a	n/a
45	BCL3	chr2:10545365-10546205	A549	lung:	n/a	n/a
46	BCLAF1	chr2:10574977-10575482	GM12878	blood:	n/a	n/a
47	BCLAF1	chr2:10579388-10580318	K562	blood:	n/a	n/a
48	BCLAF1	chr2:10550287-10550839	GM12878	blood:	n/a	chr2:10550647-10550656
49	BCLAF1	chr2:10547946-10548469	GM12878	blood:	n/a	chr2:10548264-10548273
50	BCLAF1	chr2:10578936-10579347	GM12878	blood:	n/a	n/a

(count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10567628-10567678	T-47D	breast:	n/a
2	chr2:10581770-10581820	HAEpiC	amniotic membrane:	n/a
3	chr2:10572524-10572574	U87	brain:	n/a
4	chr2:10572946-10572996	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:10566602-10566652	AG04450	lung:	fetal
6	chr2:10535858-10535908	Hepatocyte	liver:	n/a
7	chr2:10567628-10567678	T-47D	breast:	n/a
8	chr2:10581770-10581820	HAEpiC	amniotic membrane:	n/a
9	chr2:10572524-10572574	U87	brain:	n/a
10	chr2:10572946-10572996	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:10566602-10566652	AG04450	lung:	fetal
12	chr2:10535858-10535908	Hepatocyte	liver:	n/a
13	chr2:10559756-10559806	GM12892	blood:	n/a
14	chr2:10566602-10566652	AoSMC	blood vessel:	n/a
15	chr2:10567843-10567893	HAEpiC	amniotic membrane:	n/a
16	chr2:10566553-10566603	AG09309	skin:	n/a
17	chr2:10569124-10569174	AG04450	lung:	fetal
18	chr2:10567750-10567800	HIPEpiC	eye:	n/a
19	chr2:10575762-10575812	PrEC	prostate:	n/a
20	chr2:10567843-10567893	HRCEpiC	kidney:	n/a
21	chr2:10581770-10581820	HUVEC	blood vessel:	n/a
22	chr2:10569124-10569174	HEEpiC	esophagus:	n/a
23	chr2:10567526-10567576	SK-N-MC	brain:	n/a
24	chr2:10567147-10567197	U87	brain:	n/a
25	chr2:10566553-10566603	SK-N-SH_RA	brain:	n/a
26	chr2:10559669-10559719	NHBE	bronchial:	n/a
27	chr2:10570059-10570109	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:10567273-10567323	HNPCEpiC	eye:	n/a
29	chr2:10556515-10556565	PFSK-1	brain:	n/a
30	chr2:10566989-10567039	HAEpiC	amniotic membrane:	n/a
31	chr2:10535668-10535718	MCF-7	breast:	n/a
32	chr2:10567628-10567678	A549	lung:	n/a
33	chr2:10536115-10536165	HIPEpiC	eye:	n/a
34	chr2:10561359-10561409	Hepatocyte	liver:	n/a
35	chr2:10566949-10566999	PFSK-1	brain:	n/a
36	chr2:10581667-10581717	CMK	blood:	n/a
37	chr2:10567750-10567800	U87	brain:	n/a
38	chr2:10566553-10566603	HUVEC	blood vessel:	n/a
39	chr2:10559952-10560002	HEEpiC	esophagus:	n/a
40	chr2:10574659-10574709	HCT-116	colon:	n/a
41	chr2:10574659-10574709	AG09319	gingival:	n/a
42	chr2:10569124-10569174	HCF	heart:	n/a
43	chr2:10574659-10574709	K562	blood:	n/a
44	chr2:10575762-10575812	GM12892	blood:	n/a
45	chr2:10535858-10535908	HRCEpiC	kidney:	n/a
46	chr2:10556515-10556565	T-47D	breast:	n/a
47	chr2:10581667-10581717	SK-N-SH_RA	brain:	n/a
48	chr2:10567750-10567800	HAEpiC	amniotic membrane:	n/a
49	chr2:10545065-10545115	IMR90	lung:	fetal
50	chr2:10549521-10549571	U87	brain:	n/a

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr2:10456898..10458578-chr2:10575165..10577020,2	K562	blood:
2	chr2:10335310..10337198-chr2:10565374..10566915,2	K562	blood:
3	chr2:10443015..10443811-chr2:10545353..10546173,3	MCF-7	breast:
4	chr2:10416484..10418101-chr2:10547563..10549707,2	MCF-7	breast:
5	chr2:10579413..10581262-chr2:10676249..10678549,2	K562	blood:
6	chr2:10409606..10412546-chr2:10546766..10549181,2	MCF-7	breast:
7	chr2:10571135..10572690-chr2:10575390..10577231,2	K562	blood:
8	chr2:10535464..10537756-chr2:10546210..10548957,2	K562	blood:
9	chr2:10419219..10421556-chr2:10576829..10579033,2	K562	blood:
10	chr2:10580034..10581693-chr2:10583711..10585512,2	MCF-7	breast:
11	chr2:10561260..10564585-chr2:10565466..10568336,3	MCF-7	breast:
12	chr2:10531886..10534694-chr2:10548127..10550273,2	K562	blood:
13	chr2:10535204..10537517-chr2:10547562..10550495,2	MCF-7	breast:
14	chr2:10258799..10263617-chr2:10570053..10575857,8	MCF-7	breast:
15	chr2:10498534..10501300-chr2:10547746..10549393,2	K562	blood:
16	chr2:10265098..10266000-chr2:10549288..10549837,2	MCF-7	breast:
17	chr2:10553085..10555070-chr2:10555415..10558932,3	MCF-7	breast:
18	chr2:10577312..10579046-chr2:10586617..10588445,2	MCF-7	breast:
19	chr2:10539200..10541759-chr2:10543040..10545009,3	K562	blood:
20	chr2:10518586..10521002-chr2:10545177..10547256,3	MCF-7	breast:
21	chr2:10262824..10265094-chr2:10557551..10560523,2	K562	blood:
22	chr2:10547359..10549276-chr2:10571069..10572635,2	MCF-7	breast:
23	chr2:10546313..10548622-chr2:10549795..10552775,2	K562	blood:
24	chr15:45003284..45004161-chr2:10548230..10548988,2	Hela-S3	cervix:
25	chr2:10259324..10265273-chr2:10547206..10552383,9	K562	blood:
26	chr2:10268261..10270412-chr2:10564291..10566012,3	K562	blood:
27	chr2:10272230..10274773-chr2:10544365..10546593,2	MCF-7	breast:
28	chr2:10571135..10572690-chr2:10575390..10577231,2	K562	blood:
29	chr2:10359643..10362171-chr2:10579070..10581168,2	K562	blood:
30	chr2:10273185..10278025-chr2:10572544..10579398,11	K562	blood:
31	chr2:10328150..10328991-chr2:10548904..10549863,5	MCF-7	breast:
32	chr2:10495772..10497357-chr2:10549432..10551731,2	K562	blood:
33	chr2:10442217..10445067-chr2:10565919..10568177,2	MCF-7	breast:
34	chr2:10444615..10447130-chr2:10577332..10580177,3	K562	blood:
35	chr2:10442266..10443520-chr2:10548955..10549705,3	MCF-7	breast:
36	chr2:10410367..10411323-chr2:10548606..10549914,5	K562	blood:
37	chr2:10296675..10298215-chr2:10573676..10576663,2	K562	blood:
38	chr2:10211139..10213662-chr2:10577265..10580581,3	K562	blood:
39	chr2:10537541..10541103-chr2:10547321..10550436,3	MCF-7	breast:
40	chr2:10212447..10213410-chr2:10575150..10575717,2	MCF-7	breast:
41	chr2:10576992..10579344-chr2:10785593..10787982,2	K562	blood:
42	chr1:151881565..151882078-chr2:10571567..10572355,2	Hela-S3	cervix:
43	chr2:10547359..10549276-chr2:10571069..10572635,2	MCF-7	breast:
44	chr2:10277705..10280483-chr2:10573985..10576380,2	MCF-7	breast:
45	chr2:10578985..10581205-chr2:10807616..10809942,2	K562	blood:
46	chr2:10328070..10328961-chr2:10549008..10550652,5	MCF-7	breast:
47	chr2:10547842..10550365-chr2:10556156..10557846,2	K562	blood:
48	chr2:10212431..10213322-chr2:10574736..10575754,5	K562	blood:
49	chr2:10410711..10412312-chr2:10545552..10547500,2	K562	blood:
50	chr2:10531124..10533976-chr2:10546440..10548143,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HPCAL1-3	chr2:10573351-10573539	NONHSAT069099
2	lnc-HPCAL1-3	chr2:10573604-10573956	NONHSAT069099

No data

Variant related genes	Relation type
HPCAL1	TF binding region
HPCAL1	CpG island
ENSG00000163009	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000264030	chromatin interactions
ENSG00000229474	chromatin interactions
ENSG00000206633	chromatin interactions
ENSG00000159445	chromatin interactions
ENSG00000115758	chromatin interactions
ENSG00000115756	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000166710	chromatin interactions
ENSG00000257135	chromatin interactions
ENSG00000233502	chromatin interactions
ENSG00000205795	chromatin interactions
TDP1	miRNA target sites

Extended variants
information (count: 2165 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2165 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11686947	chr2:10535481-10535482	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564113565	chr2:10535493-10535494	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs533995056	chr2:10535536-10535537	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs183168339	chr2:10535542-10535543	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs550965912	chr2:10535543-10535544	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569411104	chr2:10535544-10535545	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs187701782	chr2:10535554-10535555	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs577068081	chr2:10535555-10535556	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs555515675	chr2:10535570-10535571	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138749908	chr2:10535574-10535575	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs6741475	chr2:10535607-10535608	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs556176193	chr2:10535649-10535650	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs575679349	chr2:10535660-10535661	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs552948103	chr2:10535672-10535673	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577999615	chr2:10535675-10535676	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563278407	chr2:10535715-10535716	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs10192946	chr2:10535716-10535717	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs575795160	chr2:10535763-10535764	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs542785456	chr2:10535768-10535769	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs561457336	chr2:10535776-10535777	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs541408566	chr2:10535803-10535804	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs144675907	chr2:10535805-10535806	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs16856193	chr2:10535822-10535823	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs114197416	chr2:10535832-10535833	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs532714519	chr2:10535858-10535859	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs373652031	chr2:10535897-10535898	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs550953651	chr2:10535948-10535949	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs112272170	chr2:10535951-10535952	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs191220779	chr2:10535971-10535972	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs548769314	chr2:10535978-10535979	Weak transcription Enhancers Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs183429201	chr2:10536014-10536015	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs187752361	chr2:10536027-10536028	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs546817891	chr2:10536041-10536042	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs565850320	chr2:10536061-10536062	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs571554827	chr2:10536089-10536090	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs527355681	chr2:10536106-10536107	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs372016650	chr2:10536115-10536116	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs115061266	chr2:10536145-10536146	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs557373530	chr2:10536147-10536148	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs192305387	chr2:10536190-10536191	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs536669281	chr2:10536203-10536204	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs112414705	chr2:10536226-10536227	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs554724917	chr2:10536227-10536228	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs541266534	chr2:10536244-10536245	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs573291265	chr2:10536295-10536296	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs540467883	chr2:10536316-10536317	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs565180647	chr2:10536317-10536318	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs113715742	chr2:10536319-10536320	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs544473700	chr2:10536340-10536341	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs115489877	chr2:10536344-10536345	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	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
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923524	CNVD
Pancreatic cancer	17952125	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10523000-10541000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:10523400-10537800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr2:10523600-10539000	Weak transcription	Thymus	Thymus
4	chr2:10524800-10536200	Weak transcription	Primary T cells from cord blood	blood
5	chr2:10526800-10537400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr2:10527200-10542400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr2:10527600-10536200	Weak transcription	Fetal Stomach	stomach
8	chr2:10530000-10540800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr2:10530200-10536000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr2:10530400-10537600	Weak transcription	Psoas Muscle	Psoas
11	chr2:10530400-10538800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr2:10530400-10540800	Weak transcription	Colon Smooth Muscle	Colon
13	chr2:10530600-10539800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:10530600-10544400	Weak transcription	Brain Angular Gyrus	brain
15	chr2:10531000-10536000	Weak transcription	GM12878-XiMat	blood
16	chr2:10531000-10539800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:10531000-10540600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr2:10531000-10542400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:10531000-10544600	Weak transcription	NHLF	lung
20	chr2:10531200-10539800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr2:10531200-10542400	Weak transcription	HSMMtube	muscle
22	chr2:10531200-10542400	Weak transcription	NH-A	brain
23	chr2:10531200-10544200	Weak transcription	Brain Substantia Nigra	brain
24	chr2:10531400-10539800	Weak transcription	HSMM	muscle
25	chr2:10531400-10541600	Weak transcription	Osteobl	bone
26	chr2:10532800-10537800	Enhancers	Primary T cells fromperipheralblood	blood
27	chr2:10533000-10540200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr2:10533000-10551800	Weak transcription	Ovary	ovary
29	chr2:10533400-10549200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:10533600-10536800	Weak transcription	Primary B cells from cord blood	blood
31	chr2:10533600-10537000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr2:10533600-10537000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr2:10533600-10538400	Weak transcription	Primary hematopoietic stem cells	blood
34	chr2:10533600-10539800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr2:10533600-10539800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr2:10533600-10544200	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr2:10533600-10544200	Weak transcription	Fetal Brain Female	brain
38	chr2:10533800-10535800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:10533800-10536000	Weak transcription	Gastric	stomach
40	chr2:10533800-10536200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr2:10533800-10536200	Weak transcription	Right Ventricle	heart
42	chr2:10533800-10536400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr2:10533800-10536400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:10533800-10537000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:10533800-10537400	Weak transcription	Fetal Muscle Leg	muscle
46	chr2:10533800-10537600	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr2:10533800-10537800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr2:10533800-10538200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr2:10533800-10538600	Weak transcription	Fetal Intestine Large	intestine
50	chr2:10533800-10538800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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