Variant report

Variant	nsv1045057
Chromosome Location	chr11:86794670-87033779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1601)
CpG islands
(count:61)
Chromatin interactive
region (count:69)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1601 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:86901984-86902332	K562	blood:	n/a	n/a
2	ARID3A	chr11:86808565-86809024	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:87011415-87011637	K562	blood:	n/a	n/a
4	ARID3A	chr11:87001268-87001774	K562	blood:	n/a	chr11:87001403-87001419
5	ARID3A	chr11:86904903-86905110	K562	blood:	n/a	n/a
6	ARID3A	chr11:86944770-86944904	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:86884421-86884672	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:86839305-86839814	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:87001358-87001863	HepG2	liver:	n/a	chr11:87001403-87001419
10	ARID3A	chr11:86808596-86809092	K562	blood:	n/a	n/a
11	ARID3A	chr11:86861511-86861769	HepG2	liver:	n/a	n/a
12	ATF1	chr11:86926393-86926477	K562	blood:	n/a	n/a
13	ATF1	chr11:86808580-86808925	K562	blood:	n/a	n/a
14	ATF1	chr11:87001481-87001810	K562	blood:	n/a	n/a
15	ATF1	chr11:86992567-86992847	K562	blood:	n/a	n/a
16	ATF1	chr11:86977830-86978145	K562	blood:	n/a	n/a
17	ATF1	chr11:86902082-86902330	K562	blood:	n/a	n/a
18	ATF3	chr11:86977766-86978150	K562	blood:	n/a	n/a
19	ATF3	chr11:86803222-86803489	K562	blood:	n/a	n/a
20	ATF3	chr11:87026309-87026572	K562	blood:	n/a	chr11:87026465-87026474
21	BACH1	chr11:86835199-86835457	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr11:86805450-86805451	K562	blood:	n/a	n/a
23	BACH1	chr11:86950832-86950861	K562	blood:	n/a	n/a
24	BACH1	chr11:87013438-87013541	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr11:86808725-86808892	K562	blood:	n/a	n/a
26	BACH1	chr11:86859343-86859398	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr11:87006356-87006585	GM12878	blood:	n/a	n/a
28	BCL3	chr11:86884209-86884921	A549	lung:	n/a	n/a
29	BHLHE40	chr11:86808720-86808888	K562	blood:	n/a	n/a
30	BHLHE40	chr11:86902070-86902395	K562	blood:	n/a	n/a
31	BRCA1	chr11:86884212-86885082	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr11:86884217-86885173	HCT-116	colon:	n/a	n/a
33	CBX3	chr11:86943417-86943753	K562	blood:	n/a	n/a
34	CBX3	chr11:86808476-86808990	K562	blood:	n/a	n/a
35	CBX3	chr11:86884234-86885151	HCT-116	colon:	n/a	n/a
36	CBX3	chr11:86901982-86902385	K562	blood:	n/a	n/a
37	CBX3	chr11:86797796-86798165	K562	blood:	n/a	n/a
38	CCNT2	chr11:86808679-86808904	K562	blood:	n/a	n/a
39	CCNT2	chr11:87011981-87012237	K562	blood:	n/a	n/a
40	CCNT2	chr11:86885754-86886111	K562	blood:	n/a	n/a
41	CEBPB	chr11:86992654-86992869	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr11:86994770-86994961	K562	blood:	n/a	n/a
43	CEBPB	chr11:87018244-87018529	A549	lung:	n/a	chr11:87018359-87018372 chr11:87018361-87018370 chr11:87018360-87018371
44	CEBPB	chr11:86811816-86811879	K562	blood:	n/a	n/a
45	CEBPB	chr11:86973934-86974184	K562	blood:	n/a	n/a
46	CEBPB	chr11:87026387-87026626	A549	lung:	n/a	chr11:87026455-87026466
47	CEBPB	chr11:86977799-86978091	K562	blood:	n/a	n/a
48	CEBPB	chr11:87001530-87001960	K562	blood:	n/a	chr11:87001779-87001790 chr11:87001778-87001791 chr11:87001778-87001791
49	CEBPB	chr11:86992611-86992934	A549	lung:	n/a	n/a
50	CEBPB	chr11:86892306-86892696	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:87002864-87002914	HIPEpiC	eye:	n/a
2	chr11:87002864-87002914	NHDF-neo	bronchial:	n/a
3	chr11:87002864-87002914	MCF10A-Er-Src	breast:	n/a
4	chr11:87002864-87002914	NB4	blood:	n/a
5	chr11:87002864-87002914	SK-N-SH_RA	brain:	n/a
6	chr11:87002864-87002914	HRPEpiC	eye:	n/a
7	chr11:87002864-87002914	H1-hESC	embryonic stem cell:	embryo
8	chr11:87002864-87002914	BJ	skin:	n/a
9	chr11:87002864-87002914	AG04450	lung:	fetal
10	chr11:87002864-87002914	HEEpiC	esophagus:	n/a
11	chr11:87002864-87002914	GM12891	blood:	n/a
12	chr11:87002864-87002914	T-47D	breast:	n/a
13	chr11:87002864-87002914	HCT-116	colon:	n/a
14	chr11:87002864-87002914	Jurkat	blood:	n/a
15	chr11:87002864-87002914	Hepatocyte	liver:	n/a
16	chr11:87002864-87002914	HNPCEpiC	eye:	n/a
17	chr11:87002864-87002914	ECC-1	luminal epithelium:	n/a
18	chr11:87002864-87002914	HCM	heart:	n/a
19	chr11:87002864-87002914	AG09309	skin:	n/a
20	chr11:87002864-87002914	NHBE	bronchial:	n/a
21	chr11:87002864-87002914	ProgFib	skin:	n/a
22	chr11:87002864-87002914	SK-N-MC	brain:	n/a
23	chr11:87002864-87002914	Hela-S3	cervix:	n/a
24	chr11:87002864-87002914	LNCaP	prostate:	n/a
25	chr11:87002864-87002914	GM12878	blood:	n/a
26	chr11:87002864-87002914	HEK293	kidney:	embryo
27	chr11:87002864-87002914	Caco-2	colon:	n/a
28	chr11:87002864-87002914	HRCEpiC	kidney:	n/a
29	chr11:87002864-87002914	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:87002864-87002914	GM12892	blood:	n/a
31	chr11:87002864-87002914	U87	brain:	n/a
32	chr11:87002864-87002914	RPTEC	kidney:	n/a
33	chr11:87002864-87002914	PrEC	prostate:	n/a
34	chr11:87002864-87002914	HRE	kidney:	n/a
35	chr11:87002864-87002914	HL-60	blood:	n/a
36	chr11:87002864-87002914	IMR90	lung:	fetal
37	chr11:87002864-87002914	HMEC	breast:	n/a
38	chr11:87002864-87002914	GM19239	blood:	n/a
39	chr11:87002864-87002914	AoSMC	blood vessel:	n/a
40	chr11:87002864-87002914	HAEpiC	amniotic membrane:	n/a
41	chr11:87002864-87002914	HCF	heart:	n/a
42	chr11:87002864-87002914	ovcar-3	ovarian:	n/a
43	chr11:87002864-87002914	SAEC	small airway:	n/a
44	chr11:87002864-87002914	AG10803	skin:	n/a
45	chr11:87002864-87002914	AG09319	gingival:	n/a
46	chr11:87002864-87002914	A549	lung:	n/a
47	chr11:87002864-87002914	GM06990	blood:	n/a
48	chr11:87002864-87002914	NT2-D1	testis:	n/a
49	chr11:87002864-87002914	HepG2	liver:	n/a
50	chr11:87002864-87002914	PFSK-1	brain:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:87001464..87002001-chr7:75943410..75944161,2	K562	blood:
2	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
3	chr11:86805484..86807360-chr11:87007311..87009404,2	MCF-7	breast:
4	chr11:86689677..86690529-chr11:87011689..87012195,2	MCF-7	breast:
5	chr11:86921997..86925633-chr11:86926619..86929927,5	K562	blood:
6	chr11:86664990..86667056-chr11:86996903..86999848,2	K562	blood:
7	chr11:86798772..86800664-chr11:86801632..86803429,2	K562	blood:
8	chr11:86936889..86939702-chr11:86940206..86942335,2	K562	blood:
9	chr11:86809033..86811037-chr11:86814602..86817030,2	K562	blood:
10	chr11:86664322..86666678-chr11:86802389..86805418,3	MCF-7	breast:
11	chr11:86803340..86806124-chr11:86810035..86812567,2	K562	blood:
12	chr11:86889371..86892096-chr11:86895507..86898091,3	K562	blood:
13	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:
14	chr11:86805484..86807360-chr11:87007311..87009404,2	MCF-7	breast:
15	chr11:86779436..86781916-chr11:86820681..86823632,2	K562	blood:
16	chr11:86166836..86167387-chr11:87001058..87001771,2	K562	blood:
17	chr11:87019923..87022315-chr11:87031348..87034093,2	K562	blood:
18	chr11:86899712..86901382-chr11:86903626..86906084,2	K562	blood:
19	chr11:86664953..86668319-chr11:86999800..87002548,3	MCF-7	breast:
20	chr11:86840088..86842543-chr11:86845796..86847320,2	K562	blood:
21	chr11:86665223..86667347-chr11:87003604..87005762,3	MCF-7	breast:
22	chr11:86847845..86849686-chr11:86851887..86854201,2	MCF-7	breast:
23	chr11:86921997..86925633-chr11:86926619..86929927,5	K562	blood:
24	chr11:86809033..86811037-chr11:86814602..86817030,2	K562	blood:
25	chr11:86840088..86842543-chr11:86845796..86847320,2	K562	blood:
26	chr11:86920351..86922677-chr11:86924131..86926585,2	K562	blood:
27	chr11:86641346..86643236-chr11:86990430..86992858,2	K562	blood:
28	chr11:86991946..86992672-chr5:176296643..176297235,2	MCF-7	breast:
29	chr11:86921997..86924234-chr11:86927310..86928877,2	K562	blood:
30	chr11:87019923..87022315-chr11:87031348..87034093,2	K562	blood:
31	chr11:86895352..86897026-chr11:86899805..86901720,2	K562	blood:
32	chr11:86972962..86974479-chr11:86976089..86977632,2	MCF-7	breast:
33	chr11:86867900..86869412-chr11:86871775..86874240,2	K562	blood:
34	chr11:87033511..87035138-chr11:87075448..87077879,2	K562	blood:
35	chr11:86889371..86892096-chr11:86895507..86898091,3	K562	blood:
36	chr11:86900182..86903492-chr11:86905711..86910083,4	K562	blood:
37	chr11:86810025..86812420-chr11:86813811..86815830,2	K562	blood:
38	chr11:86818728..86820494-chr11:86831907..86834474,2	K562	blood:
39	chr11:86806619..86807569-chr11:86992272..86993052,3	MCF-7	breast:
40	chr11:86664855..86666701-chr11:87000839..87002926,2	MCF-7	breast:
41	chr11:86924206..86926245-chr11:86930378..86932580,2	K562	blood:
42	chr11:86818728..86820494-chr11:86831907..86834474,2	K562	blood:
43	chr11:86900182..86903492-chr11:86905711..86910083,4	K562	blood:
44	chr11:86920351..86922677-chr11:86924131..86926585,2	K562	blood:
45	chr11:86664821..86667112-chr11:86824827..86827318,2	MCF-7	breast:
46	chr11:87028128..87030970-chr11:87034928..87037460,2	K562	blood:
47	chr11:86706337..86706967-chr11:86808249..86808967,2	K562	blood:
48	chr11:86867900..86869412-chr11:86871775..86874240,2	K562	blood:
49	chr11:86996729..86999242-chr11:87005313..87006882,2	MCF-7	breast:
50	chr11:86977540..86979356-chr11:86980303..86982155,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FZD4-6	chr11:86805776-86807627	NONHSAT023514
2	lnc-PRSS23-5	chr11:87032243-87033077	NONHSAT023517
3	lnc-FZD4-8	chr11:86969893-86970301	NONHSAT023515
4	lnc-PRSS23-5	chr11:87030109-87030419	NONHSAT023517

No data

Variant related genes	Relation type
ENSG00000213287	TF binding region
TMEM135	TF binding region
ENSG00000254843	TF binding region
ENSG00000213287	CpG island
TMEM135	CpG island
ENSG00000254843	CpG island
ENSG00000174804	chromatin interactions
ENSG00000246523	chromatin interactions
ENSG00000270510	chromatin interactions

Extended variants
information (count: 9581 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:9581 , 50 per page) page: 1 2 3 4 5 6 7 ... 192

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190602046	chr11:86794687-86794688	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs570476512	chr11:86794693-86794694	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569283728	chr11:86794711-86794712	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs539468822	chr11:86794728-86794729	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553357898	chr11:86794796-86794797	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573441130	chr11:86794820-86794821	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536183248	chr11:86794830-86794831	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375976285	chr11:86794831-86794832	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2513240	chr11:86794856-86794857	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs556969772	chr11:86794914-86794915	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557575647	chr11:86794921-86794922	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs373247275	chr11:86794935-86794936	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575915748	chr11:86794988-86794989	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572690750	chr11:86795036-86795037	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376428761	chr11:86795072-86795073	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543503358	chr11:86795083-86795084	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183752726	chr11:86795115-86795116	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188221291	chr11:86795150-86795151	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12801184	chr11:86795184-86795185	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs78691700	chr11:86795186-86795187	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs115850184	chr11:86795229-86795230	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs138497437	chr11:86795249-86795250	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573418947	chr11:86795281-86795282	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192923393	chr11:86795310-86795311	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs5793234	chr11:86795356-86795357	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs79421653	chr11:86795366-86795367	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs5793235	chr11:86795368-86795369	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573600333	chr11:86795373-86795374	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144935964	chr11:86795376-86795377	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550632374	chr11:86795389-86795390	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372558208	chr11:86795390-86795391	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs570588456	chr11:86795424-86795425	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs57664476	chr11:86795427-86795428	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs562483158	chr11:86795551-86795552	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372081107	chr11:86795580-86795581	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532930798	chr11:86795589-86795590	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs540585284	chr11:86795604-86795605	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112776407	chr11:86795607-86795608	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs2445582	chr11:86795619-86795620	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs182997555	chr11:86795664-86795665	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535730244	chr11:86795696-86795697	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556036016	chr11:86795697-86795698	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564680849	chr11:86795698-86795699	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569443333	chr11:86795712-86795713	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs2445581	chr11:86795718-86795719	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs368132225	chr11:86795748-86795749	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558418636	chr11:86795755-86795756	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs188028290	chr11:86795769-86795770	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191367172	chr11:86795780-86795781	Bivalent Enhancer Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552692309	chr11:86795822-86795823	Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	18194544	CNVD

Chromatin state (count:1983 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:86770400-86808200	Weak transcription	HUVEC	blood vessel
2	chr11:86774800-86806400	Weak transcription	Small Intestine	intestine
3	chr11:86776600-86815600	Weak transcription	HSMMtube	muscle
4	chr11:86782600-86795400	Weak transcription	Fetal Heart	heart
5	chr11:86783000-86814000	Weak transcription	Hela-S3	cervix
6	chr11:86783200-86799000	Weak transcription	Psoas Muscle	Psoas
7	chr11:86787200-86795400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:86787400-86819600	Weak transcription	NH-A	brain
9	chr11:86787600-86804200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr11:86787600-86825200	Weak transcription	Brain Substantia Nigra	brain
11	chr11:86787800-86797200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:86787800-86797200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:86787800-86798200	Weak transcription	Spleen	Spleen
14	chr11:86787800-86804000	Weak transcription	Fetal Intestine Large	intestine
15	chr11:86787800-86817400	Weak transcription	Colon Smooth Muscle	Colon
16	chr11:86787800-86819400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:86788000-86795400	Weak transcription	Lung	lung
18	chr11:86788000-86797200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:86788000-86797200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:86788000-86797200	Weak transcription	Esophagus	oesophagus
21	chr11:86788000-86797200	Weak transcription	Fetal Intestine Small	intestine
22	chr11:86788000-86797200	Weak transcription	Fetal Thymus	thymus
23	chr11:86788000-86797200	Weak transcription	Thymus	Thymus
24	chr11:86788000-86798400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr11:86788000-86800000	Weak transcription	Brain Germinal Matrix	brain
26	chr11:86788000-86800000	Weak transcription	Gastric	stomach
27	chr11:86788000-86803200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr11:86788000-86803600	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr11:86788000-86804200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr11:86788000-86804200	Weak transcription	Aorta	Aorta
31	chr11:86788000-86807000	Weak transcription	Pancreas	Pancrea
32	chr11:86788000-86808600	Weak transcription	Left Ventricle	heart
33	chr11:86788200-86795400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:86788200-86796800	Weak transcription	Fetal Muscle Leg	muscle
35	chr11:86788200-86797800	Weak transcription	Fetal Muscle Trunk	muscle
36	chr11:86788200-86797800	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr11:86788200-86808400	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr11:86788200-86817800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr11:86788200-86824600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr11:86788200-86830400	Weak transcription	Right Ventricle	heart
41	chr11:86788400-86803000	Weak transcription	NHDF-Ad	bronchial
42	chr11:86788400-86807800	Weak transcription	Brain Hippocampus Middle	brain
43	chr11:86788600-86797200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr11:86788600-86802600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr11:86788600-86804200	Weak transcription	Placenta	Placenta
46	chr11:86788600-86806000	Weak transcription	A549	lung
47	chr11:86788600-86836400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr11:86789000-86797200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr11:86789000-86797600	Weak transcription	K562	blood
50	chr11:86789000-86802600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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