Variant report

Variant	nsv553219
Chromosome Location	chr11:5026200-5214413
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1015)
CpG islands
(count:854)
Chromatin interactive
region (count:156)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:5145337-5145816	K562	blood:	n/a	n/a
2	ARID3A	chr11:5128676-5128829	K562	blood:	n/a	n/a
3	ARID3A	chr11:5181356-5181703	K562	blood:	n/a	n/a
4	ARID3A	chr11:5150153-5151193	K562	blood:	n/a	n/a
5	ARID3A	chr11:5108595-5108795	K562	blood:	n/a	n/a
6	ARID3A	chr11:5188271-5188388	K562	blood:	n/a	n/a
7	ARID3A	chr11:5151921-5153769	K562	blood:	n/a	n/a
8	ARID3A	chr11:5193260-5193372	K562	blood:	n/a	n/a
9	ARID3A	chr11:5174418-5175664	K562	blood:	n/a	n/a
10	ARID3A	chr11:5194443-5194536	K562	blood:	n/a	n/a
11	ARID3A	chr11:5172733-5173404	K562	blood:	n/a	n/a
12	ATF1	chr11:5150550-5151082	K562	blood:	n/a	n/a
13	ATF1	chr11:5172839-5173425	K562	blood:	n/a	n/a
14	ATF1	chr11:5199045-5199305	K562	blood:	n/a	n/a
15	ATF1	chr11:5080856-5080860	K562	blood:	n/a	n/a
16	ATF1	chr11:5128542-5128826	K562	blood:	n/a	n/a
17	ATF1	chr11:5153059-5153491	K562	blood:	n/a	n/a
18	ATF1	chr11:5108569-5108812	K562	blood:	n/a	n/a
19	ATF3	chr11:5181334-5181617	K562	blood:	n/a	n/a
20	ATF3	chr11:5128498-5128875	K562	blood:	n/a	n/a
21	ATF3	chr11:5150491-5151003	K562	blood:	n/a	n/a
22	BACH1	chr11:5059379-5059473	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr11:5126229-5126282	K562	blood:	n/a	n/a
24	BACH1	chr11:5153269-5154148	K562	blood:	n/a	n/a
25	BHLHE40	chr11:5114577-5114619	K562	blood:	n/a	n/a
26	BHLHE40	chr11:5193299-5193453	K562	blood:	n/a	n/a
27	BHLHE40	chr11:5145321-5145613	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:5145393-5145647	K562	blood:	n/a	n/a
29	BHLHE40	chr11:5152969-5153636	K562	blood:	n/a	n/a
30	BHLHE40	chr11:5172794-5173440	K562	blood:	n/a	n/a
31	BRCA1	chr11:5055287-5055292	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr11:5152914-5153556	K562	blood:	n/a	n/a
33	CCNT2	chr11:5175368-5175697	K562	blood:	n/a	n/a
34	CCNT2	chr11:5150752-5151154	K562	blood:	n/a	n/a
35	CCNT2	chr11:5172885-5173588	K562	blood:	n/a	n/a
36	CCNT2	chr11:5108478-5108879	K562	blood:	n/a	n/a
37	CCNT2	chr11:5181487-5181716	K562	blood:	n/a	n/a
38	CCNT2	chr11:5152975-5153809	K562	blood:	n/a	n/a
39	CCNT2	chr11:5206078-5206231	K562	blood:	n/a	n/a
40	CEBPB	chr11:5155439-5155486	K562	blood:	n/a	chr11:5155443-5155454 chr11:5155443-5155454
41	CEBPB	chr11:5150548-5150936	IMR90	lung:	n/a	chr11:5150735-5150746
42	CEBPB	chr11:5108761-5108784	K562	blood:	n/a	n/a
43	CEBPB	chr11:5145178-5145630	Hela-S3	cervix:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
44	CEBPB	chr11:5145160-5145706	A549	lung:	n/a	chr11:5145432-5145443 chr11:5145432-5145445
45	CEBPB	chr11:5150613-5150884	HepG2	liver:	n/a	chr11:5150735-5150746
46	CEBPB	chr11:5109257-5109343	K562	blood:	n/a	n/a
47	CEBPB	chr11:5152900-5153523	K562	blood:	n/a	n/a
48	CEBPB	chr11:5034272-5034625	IMR90	lung:	n/a	chr11:5034438-5034447 chr11:5034436-5034449 chr11:5034436-5034449 chr11:5034438-5034447 chr11:5034438-5034449 chr11:5034438-5034447 chr11:5034438-5034447 chr11:5034436-5034449 chr11:5034436-5034447
49	CEBPB	chr11:5172854-5173191	K562	blood:	n/a	n/a
50	CEBPB	chr11:5145365-5145512	HepG2	liver:	n/a	chr11:5145432-5145443 chr11:5145432-5145445

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5153834-5153884	HRE	kidney:	n/a
2	chr11:5153834-5153884	HPAEpiC	pulmonary alveolar:	n/a
3	chr11:5173605-5173655	HIPEpiC	eye:	n/a
4	chr11:5166758-5166808	HMEC	breast:	n/a
5	chr11:5080941-5080991	K562	blood:	n/a
6	chr11:5165693-5165743	HEK293	kidney:	embryo
7	chr11:5080941-5080991	IMR90	lung:	fetal
8	chr11:5165693-5165743	HEEpiC	esophagus:	n/a
9	chr11:5067183-5067233	HUVEC	blood vessel:	n/a
10	chr11:5067183-5067233	K562	blood:	n/a
11	chr11:5080941-5080991	HEK293	kidney:	embryo
12	chr11:5165693-5165743	HRE	kidney:	n/a
13	chr11:5067039-5067089	PrEC	prostate:	n/a
14	chr11:5174413-5174463	SK-N-SH_RA	brain:	n/a
15	chr11:5067039-5067089	RPTEC	kidney:	n/a
16	chr11:5174413-5174463	HCPEpiC	choroid plexus:	n/a
17	chr11:5143555-5143605	GM12878	blood:	n/a
18	chr11:5153834-5153884	AG09309	skin:	n/a
19	chr11:5143555-5143605	CMK	blood:	n/a
20	chr11:5142602-5142652	Hepatocyte	liver:	n/a
21	chr11:5165693-5165743	PFSK-1	brain:	n/a
22	chr11:5067927-5067977	GM12891	blood:	n/a
23	chr11:5166758-5166808	SK-N-SH	brain:	n/a
24	chr11:5080452-5080502	HNPCEpiC	eye:	n/a
25	chr11:5142602-5142652	NB4	blood:	n/a
26	chr11:5142602-5142652	A549	lung:	n/a
27	chr11:5067927-5067977	Hepatocyte	liver:	n/a
28	chr11:5173605-5173655	SK-N-MC	brain:	n/a
29	chr11:5067927-5067977	ovcar-3	ovarian:	n/a
30	chr11:5080452-5080502	NH-A	brain:	n/a
31	chr11:5173436-5173486	GM12892	blood:	n/a
32	chr11:5067183-5067233	NH-A	brain:	n/a
33	chr11:5080452-5080502	HL-60	blood:	n/a
34	chr11:5080452-5080502	MCF-7	breast:	n/a
35	chr11:5080941-5080991	HRPEpiC	eye:	n/a
36	chr11:5173605-5173655	SAEC	small airway:	n/a
37	chr11:5067183-5067233	PFSK-1	brain:	n/a
38	chr11:5174413-5174463	A549	lung:	n/a
39	chr11:5067183-5067233	GM06990	blood:	n/a
40	chr11:5142602-5142652	GM12891	blood:	n/a
41	chr11:5143555-5143605	HEEpiC	esophagus:	n/a
42	chr11:5173436-5173486	CMK	blood:	n/a
43	chr11:5166758-5166808	NT2-D1	testis:	n/a
44	chr11:5174413-5174463	H1-hESC	embryonic stem cell:	embryo
45	chr11:5144101-5144151	HL-60	blood:	n/a
46	chr11:5165693-5165743	GM06990	blood:	n/a
47	chr11:5173436-5173486	H1-hESC	embryonic stem cell:	embryo
48	chr11:5153834-5153884	HCM	heart:	n/a
49	chr11:5142602-5142652	MCF-7	breast:	n/a
50	chr11:5067039-5067089	CMK	blood:	n/a

(count:156 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5150699..5153256-chr11:5166471..5169449,2	K562	blood:
2	chr11:5166640..5168909-chr11:5173879..5175429,2	K562	blood:
3	chr11:5124860..5127812-chr11:5127932..5129451,2	K562	blood:
4	chr11:5042377..5044807-chr11:5046869..5048833,2	K562	blood:
5	chr11:5140099..5148928-chr11:5149317..5155604,15	K562	blood:
6	chr11:5150178..5155699-chr11:5220911..5225581,8	K562	blood:
7	11:5033143-5038367..11:5721056-5732713	GM12878	blood:
8	11:5033143-5038367..11:5250847-5268367	Hela-S3	cervix:
9	chr11:5124860..5127812-chr11:5127932..5129451,2	K562	blood:
10	11:5020673-5032983..11:5700314-5707362	K562	blood:
11	chr11:5149719..5151749-chr11:5525056..5527952,2	K562	blood:
12	11:5033143-5038367..11:5600743-5604452	Hela-S3	cervix:
13	11:5033143-5038367..11:5700314-5707362	K562	blood:
14	chr11:5140099..5148928-chr11:5149317..5155604,15	K562	blood:
15	11:5020673-5032983..11:5527719-5533869	K562	blood:
16	chr11:5163035..5164810-chr11:5166036..5168389,2	K562	blood:
17	chr11:5170640..5172644-chr11:5176935..5178921,2	K562	blood:
18	chr11:5186471..5188336-chr11:5192337..5194748,2	K562	blood:
19	chr11:4918642..4921294-chr11:5101983..5104188,2	K562	blood:
20	chr11:4658272..4658813-chr11:5025400..5026262,2	MCF-7	breast:
21	chr11:4208337..4209114-chr11:5025486..5026266,2	MCF-7	breast:
22	11:5137223-5140360..11:5566274-5571131	Hela-S3	cervix:
23	11:5137223-5140360..11:5721056-5732713	GM12878	blood:
24	11:5154908-5159254..11:5721056-5732713	GM12878	blood:
25	chr11:5058379..5061279-chr11:5093640..5097390,3	K562	blood:
26	chr11:5104003..5106355-chr11:5107356..5109322,2	K562	blood:
27	chr11:5075968..5078829-chr11:5086090..5088506,2	K562	blood:
28	chr11:5163553..5165336-chr11:5177083..5178802,2	K562	blood:
29	chr11:5151017..5154048-chr11:5172575..5176593,5	K562	blood:
30	chr11:5150382..5152243-chr11:5521583..5523771,2	K562	blood:
31	11:5134474-5137223..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
32	11:5020673-5032983..11:5721056-5732713	K562	blood:
33	11:5033143-5038367..11:5363591-5368290	Hela-S3	cervix:
34	chr11:5143402..5145661-chr11:5288331..5290238,2	K562	blood:
35	chr11:5167216..5169602-chr11:5170013..5172866,3	K562	blood:
36	chr11:5117503..5120431-chr11:5123925..5125786,2	K562	blood:
37	chr11:5107926..5109438-chr11:5115922..5117651,2	K562	blood:
38	chr11:5176158..5179141-chr6:31164064..31167206,3	K562	blood:
39	chr11:5154058..5156927-chr11:5244271..5247136,2	K562	blood:
40	chr11:5075968..5078829-chr11:5086090..5088506,2	K562	blood:
41	chr11:5171363..5173809-chr11:5174253..5176049,3	K562	blood:
42	chr11:5150801..5152523-chr11:5295728..5297239,2	K562	blood:
43	chr11:5155212..5157453-chr11:5171117..5172867,2	K562	blood:
44	chr11:4647527..4648151-chr11:5025801..5026495,2	MCF-7	breast:
45	chr11:5167216..5169602-chr11:5170013..5172866,3	K562	blood:
46	chr11:5143364..5146967-chr11:5150857..5153670,3	K562	blood:
47	chr11:5106264..5108013-chr11:5110270..5111995,2	K562	blood:
48	chr11:5150699..5153256-chr11:5166471..5169449,2	K562	blood:
49	11:5093737-5099374..11:5250847-5268367	Hela-S3	cervix:
50	11:4869840-4870943..11:5020673-5032983	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR52E2-1	chr11:5083868-5084643	NONHSAT017660
2	lnc-OR52A5-1	chr11:5127292-5128067	XLOC_009364
3	lnc-OR52E2-1	chr11:5085244-5085336	NONHSAT017660
4	lnc-OR52A5-1	chr11:5128668-5128760	XLOC_009364

No data

Variant related genes	Relation type
OR52A5	TF binding region
OR52Z1	TF binding region
OR52E3P	TF binding region
OR52E1	TF binding region
ENSG00000236897	TF binding region
OR51A1P	TF binding region
OR52A1	TF binding region
OR52J1P	TF binding region
OR52S1P	TF binding region
OR52J3	TF binding region
OR52J2P	TF binding region
OR52A4	TF binding region
OR51P1P	TF binding region
ENSG00000273085	TF binding region
OR52E2	TF binding region
OR52A5	CpG island
OR52Z1	CpG island
OR52E3P	CpG island
OR52E1	CpG island
ENSG00000236897	CpG island
OR51A1P	CpG island
OR52A1	CpG island
OR52J1P	CpG island
OR52S1P	CpG island
OR52J3	CpG island
OR52J2P	CpG island
OR52A4	CpG island
OR51P1P	CpG island
ENSG00000273085	CpG island
OR52E2	CpG island
ENSG00000242180	chromatin interactions
ENSG00000181616	chromatin interactions
ENSG00000182070	chromatin interactions
ENSG00000203560	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000176748	chromatin interactions
ENSG00000187747	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000181609	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000272501	chromatin interactions
ENSG00000176752	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000254480	chromatin interactions
ENSG00000176787	chromatin interactions
ENSG00000176922	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000176900	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000236897	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000188069	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000273085	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000205494	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000176798	chromatin interactions
ENSG00000236359	chromatin interactions
ENSG00000226157	chromatin interactions
ENSG00000206344	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000184698	chromatin interactions
ARID3B	miRNA target sites

Extended variants
information (count: 5622 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5622 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10837119	chr11:5026200-5026201	Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569062921	chr11:5026282-5026283	Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs183649170	chr11:5026317-5026318	Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs532221787	chr11:5026375-5026376	Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs566643987	chr11:5026443-5026444	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs140968193	chr11:5026453-5026454	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs34602924	chr11:5026454-5026455	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs189151661	chr11:5026500-5026501	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs182034155	chr11:5026502-5026503	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs145986977	chr11:5026503-5026504	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs557276405	chr11:5026508-5026509	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs551216287	chr11:5026538-5026539	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs540090649	chr11:5026539-5026540	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs185839266	chr11:5026563-5026564	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs189078835	chr11:5026564-5026565	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs540373995	chr11:5026571-5026572	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs561755813	chr11:5026577-5026578	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs138795340	chr11:5026600-5026601	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs75539333	chr11:5026661-5026662	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs562473025	chr11:5026679-5026680	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs533112844	chr11:5026684-5026685	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs551632067	chr11:5026691-5026692	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs2499955	chr11:5026767-5026768	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs572827418	chr11:5026775-5026776	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs548728508	chr11:5026778-5026779	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs568217144	chr11:5026783-5026784	Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs181209434	chr11:5026804-5026805	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs186413685	chr11:5026812-5026813	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs569218134	chr11:5026820-5026821	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs142919312	chr11:5026826-5026827	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs191236740	chr11:5026940-5026941	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs573514824	chr11:5026962-5026963	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs182635623	chr11:5026963-5026964	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs555971366	chr11:5027022-5027023	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs573798470	chr11:5027023-5027024	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs544311113	chr11:5027113-5027114	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs373867053	chr11:5027143-5027144	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs75030874	chr11:5027155-5027156	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs562373223	chr11:5027172-5027173	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs550817272	chr11:5027197-5027198	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs115512303	chr11:5027198-5027199	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs76422887	chr11:5027245-5027246	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs560406232	chr11:5027284-5027285	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs72860895	chr11:5027289-5027290	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs34419397	chr11:5027303-5027304	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs147005393	chr11:5027314-5027315	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs185317598	chr11:5027402-5027403	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs560714336	chr11:5027516-5027517	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs58083716	chr11:5027535-5027536	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs529380200	chr11:5027547-5027548	Inactive region	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5025800-5026400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:5026000-5026800	Enhancers	NHEK	skin
3	chr11:5026200-5026800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:5026200-5026800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:5026200-5026800	Enhancers	HMEC	breast
6	chr11:5026400-5026800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:5033000-5033800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:5042400-5043200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
9	chr11:5042800-5043400	Enhancers	Left Ventricle	heart
10	chr11:5049000-5049600	Active TSS	Fetal Heart	heart
11	chr11:5058400-5058800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:5062800-5064000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:5064400-5064800	Enhancers	HMEC	breast
14	chr11:5067800-5068200	Enhancers	Placenta	Placenta
15	chr11:5067800-5068200	Enhancers	Gastric	stomach
16	chr11:5068000-5068400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr11:5068000-5068400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr11:5068000-5068400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr11:5068000-5068400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:5068200-5068600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr11:5080400-5080800	Active TSS	Primary T killer memory cells from peripheral blood	blood
22	chr11:5084800-5085600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:5085600-5086000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:5086000-5086200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:5086200-5093000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:5091000-5091400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr11:5092800-5093200	Enhancers	Adipose Nuclei	Adipose
28	chr11:5093000-5093400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr11:5093000-5093400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr11:5093000-5093400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:5093200-5093600	Flanking Active TSS	Adipose Nuclei	Adipose
32	chr11:5093600-5094200	Enhancers	Adipose Nuclei	Adipose
33	chr11:5098000-5098200	ZNF genes & repeats	Right Atrium	heart
34	chr11:5100200-5100800	Enhancers	Liver	Liver
35	chr11:5108000-5108400	Enhancers	K562	blood
36	chr11:5108000-5108600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr11:5108200-5108400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:5108400-5108800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr11:5108400-5108800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:5108400-5109000	Flanking Active TSS	K562	blood
41	chr11:5108400-5109200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr11:5108600-5108800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr11:5108800-5109600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:5108800-5110000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:5109600-5110600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr11:5110000-5110600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:5110400-5110600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr11:5113800-5114400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:5114000-5114800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr11:5120600-5120800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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