Variant report

Variant	nsv832109
Chromosome Location	chr11:32661314-32830549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1081)
CpG islands
(count:549)
Chromatin interactive
region (count:29)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1081 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:32728333-32728791	K562	blood:	n/a	n/a
2	ARID3A	chr11:32814471-32814880	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:32728312-32729190	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:32720244-32720392	HepG2	liver:	n/a	n/a
5	ATF1	chr11:32728632-32728832	K562	blood:	n/a	n/a
6	ATF2	chr11:32728471-32728962	GM12878	blood:	n/a	n/a
7	ATF2	chr11:32728438-32728961	GM12878	blood:	n/a	n/a
8	ATF3	chr11:32728578-32728824	K562	blood:	n/a	n/a
9	BACH1	chr11:32791164-32791439	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:32791060-32791286	K562	blood:	n/a	n/a
11	BACH1	chr11:32728557-32728875	K562	blood:	n/a	chr11:32728711-32728725
12	BATF	chr11:32728598-32728852	GM12878	blood:	n/a	chr11:32728715-32728725 chr11:32728761-32728772 chr11:32728714-32728725
13	BATF	chr11:32728528-32728839	GM12878	blood:	n/a	chr11:32728715-32728725 chr11:32728761-32728772 chr11:32728714-32728725
14	BHLHE40	chr11:32738785-32738871	GM12878	blood:	n/a	n/a
15	CBX3	chr11:32728467-32729017	HCT-116	colon:	n/a	n/a
16	CBX3	chr11:32726342-32726641	K562	blood:	n/a	n/a
17	CCNT2	chr11:32808701-32808880	K562	blood:	n/a	n/a
18	CEBPB	chr11:32719883-32720143	K562	blood:	n/a	chr11:32720009-32720020
19	CEBPB	chr11:32725753-32726055	A549	lung:	n/a	n/a
20	CEBPB	chr11:32719860-32720190	HepG2	liver:	n/a	chr11:32720009-32720020
21	CEBPB	chr11:32719797-32720493	A549	lung:	n/a	chr11:32720009-32720020
22	CEBPB	chr11:32702710-32702937	A549	lung:	n/a	n/a
23	CEBPB	chr11:32719842-32720343	A549	lung:	n/a	chr11:32720009-32720020
24	CEBPB	chr11:32725773-32726100	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:32727233-32727558	A549	lung:	n/a	chr11:32727408-32727419
26	CEBPB	chr11:32702684-32702977	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:32728984-32729287	A549	lung:	n/a	chr11:32729109-32729120
28	CEBPB	chr11:32728877-32729333	A549	lung:	n/a	chr11:32729109-32729120
29	CEBPB	chr11:32727203-32727525	A549	lung:	n/a	chr11:32727408-32727419
30	CEBPB	chr11:32698756-32698921	HepG2	liver:	n/a	n/a
31	CEBPB	chr11:32728227-32729278	Hela-S3	cervix:	n/a	chr11:32729109-32729120
32	CEBPB	chr11:32727289-32727489	H1-hESC	embryonic stem cell:	n/a	chr11:32727408-32727419
33	CEBPB	chr11:32727248-32727570	K562	blood:	n/a	chr11:32727408-32727419
34	CEBPB	chr11:32727244-32727511	Hela-S3	cervix:	n/a	chr11:32727408-32727419
35	CEBPB	chr11:32703444-32703632	HepG2	liver:	n/a	chr11:32703586-32703603 chr11:32703517-32703528
36	CEBPB	chr11:32719890-32720157	IMR90	lung:	n/a	chr11:32720009-32720020
37	CEBPB	chr11:32727243-32727579	HepG2	liver:	n/a	chr11:32727408-32727419
38	CEBPB	chr11:32727254-32727548	IMR90	lung:	n/a	chr11:32727408-32727419
39	CEBPB	chr11:32719890-32720084	Hela-S3	cervix:	n/a	chr11:32720009-32720020
40	CEBPB	chr11:32719389-32719413	HepG2	liver:	n/a	n/a
41	CEBPB	chr11:32728368-32729434	HCT-116	colon:	n/a	chr11:32729109-32729120
42	CEBPB	chr11:32725759-32726078	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:32668904-32668942	ProgFib	skin:	n/a	n/a
44	CTCF	chr11:32771200-32771350	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr11:32814480-32814630	HMEC	breast:	n/a	chr11:32814606-32814615 chr11:32814602-32814615 chr11:32814600-32814618 chr11:32814603-32814613
46	CTCF	chr11:32735160-32735310	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr11:32735160-32735310	GM06990	blood:	n/a	n/a
48	CTCF	chr11:32814265-32814313	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr11:32771240-32771390	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr11:32771240-32771390	HCM	heart:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:32816227-32816277	RPTEC	kidney:	n/a
2	chr11:32816080-32816130	SK-N-MC	brain:	n/a
3	chr11:32816254-32816304	LNCaP	prostate:	n/a
4	chr11:32815865-32815915	HCM	heart:	n/a
5	chr11:32817614-32817664	ovcar-3	ovarian:	n/a
6	chr11:32817614-32817664	AG09319	gingival:	n/a
7	chr11:32816227-32816277	Jurkat	blood:	n/a
8	chr11:32816080-32816130	HEK293	kidney:	embryo
9	chr11:32815896-32815946	MCF-7	breast:	n/a
10	chr11:32817614-32817664	HCF	heart:	n/a
11	chr11:32816080-32816130	H1-hESC	embryonic stem cell:	embryo
12	chr11:32815865-32815915	GM12878	blood:	n/a
13	chr11:32816211-32816261	T-47D	breast:	n/a
14	chr11:32815865-32815915	AG09319	gingival:	n/a
15	chr11:32816254-32816304	T-47D	breast:	n/a
16	chr11:32815896-32815946	SK-N-MC	brain:	n/a
17	chr11:32816227-32816277	MCF10A-Er-Src	breast:	n/a
18	chr11:32816211-32816261	ECC-1	luminal epithelium:	n/a
19	chr11:32815968-32816018	NB4	blood:	n/a
20	chr11:32815896-32815946	GM06990	blood:	n/a
21	chr11:32816227-32816277	K562	blood:	n/a
22	chr11:32815968-32816018	Hepatocyte	liver:	n/a
23	chr11:32817614-32817664	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:32816211-32816261	H1-hESC	embryonic stem cell:	embryo
25	chr11:32817614-32817664	HRCEpiC	kidney:	n/a
26	chr11:32815968-32816018	HRE	kidney:	n/a
27	chr11:32815865-32815915	T-47D	breast:	n/a
28	chr11:32815896-32815946	Jurkat	blood:	n/a
29	chr11:32816080-32816130	AG04450	lung:	fetal
30	chr11:32815865-32815915	HCPEpiC	choroid plexus:	n/a
31	chr11:32816885-32816935	A549	lung:	n/a
32	chr11:32816227-32816277	BE2_C	brain:	n/a
33	chr11:32815865-32815915	Hepatocyte	liver:	n/a
34	chr11:32817614-32817664	GM19239	blood:	n/a
35	chr11:32817614-32817664	HL-60	blood:	n/a
36	chr11:32816227-32816277	GM12892	blood:	n/a
37	chr11:32817614-32817664	HEK293	kidney:	embryo
38	chr11:32816227-32816277	IMR90	lung:	fetal
39	chr11:32815968-32816018	HCF	heart:	n/a
40	chr11:32815968-32816018	AG04449	skin:	fetal
41	chr11:32816080-32816130	GM12891	blood:	n/a
42	chr11:32817614-32817664	HIPEpiC	eye:	n/a
43	chr11:32815896-32815946	NHBE	bronchial:	n/a
44	chr11:32815968-32816018	AG04450	lung:	fetal
45	chr11:32815896-32815946	A549	lung:	n/a
46	chr11:32815865-32815915	ovcar-3	ovarian:	n/a
47	chr11:32816254-32816304	U87	brain:	n/a
48	chr11:32816254-32816304	HEK293	kidney:	embryo
49	chr11:32815968-32816018	GM12891	blood:	n/a
50	chr11:32815896-32815946	HCPEpiC	choroid plexus:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:32659336..32661758-chr11:32663694..32666060,2	K562	blood:
2	chr11:32344866..32345612-chr11:32814115..32815021,3	K562	blood:
3	chr11:32808269..32810578-chr11:32811401..32813892,2	K562	blood:
4	chr11:32734751..32735852-chr11:32814047..32815123,4	K562	blood:
5	chr11:32734959..32735691-chr11:32814406..32814938,2	MCF-7	breast:
6	chr11:32734492..32735804-chr11:32813911..32815565,5	MCF-7	breast:
7	chr11:32605665..32608550-chr11:32673934..32676744,2	K562	blood:
8	chr11:32825967..32829445-chr11:32834509..32837119,3	K562	blood:
9	chr11:32738397..32740619-chr11:33277961..33280390,2	MCF-7	breast:
10	chr11:32814796..32817275-chr11:32819869..32822707,2	MCF-7	breast:
11	chr11:32789537..32792072-chr11:32812363..32815095,2	K562	blood:
12	chr11:32659336..32661758-chr11:32663694..32666060,2	K562	blood:
13	chr11:32808269..32810578-chr11:32811401..32813892,2	K562	blood:
14	chr11:32694547..32697464-chr11:32699936..32702319,2	K562	blood:
15	chr11:32741454..32744033-chr11:32750070..32751774,2	K562	blood:
16	chr11:32734959..32735691-chr11:32814406..32814938,2	MCF-7	breast:
17	chr11:32699830..32701629-chr11:32708970..32710563,2	K562	blood:
18	chr11:32395477..32395997-chr11:32813804..32814649,2	K562	blood:
19	chr11:32770910..32771799-chr11:32813954..32815012,4	MCF-7	breast:
20	chr11:32789537..32792072-chr11:32812363..32815095,2	K562	blood:
21	chr11:32734751..32735852-chr11:32814047..32815123,4	K562	blood:
22	chr11:32741454..32744033-chr11:32750070..32751774,2	K562	blood:
23	chr11:32797795..32799426-chr11:32913652..32916468,2	MCF-7	breast:
24	chr11:32770910..32771799-chr11:32813954..32815012,4	MCF-7	breast:
25	chr11:32699830..32701629-chr11:32708970..32710563,2	K562	blood:
26	chr11:32734492..32735804-chr11:32813911..32815565,5	MCF-7	breast:
27	chr11:32723875..32726854-chr11:32913788..32916126,2	K562	blood:
28	chr11:32704711..32706720-chr11:32913831..32915608,2	K562	blood:
29	chr11:32694547..32697464-chr11:32699936..32702319,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRRG4-3	chr11:32823241-32823497	NONHSAT018675
2	lnc-PRRG4-4	chr11:32779814-32780160	NONHSAT018673
3	lnc-CCDC73-2	chr11:32817536-32817819	NONHSAT018674

No data

Variant related genes	Relation type
CCDC73	TF binding region
ENSG00000244535	TF binding region
CCDC73	CpG island
ENSG00000244535	CpG island
ENSG00000186714	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000110422	chromatin interactions

Extended variants
information (count: 2860 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2860 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568692158	chr11:32661953-32661954	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs113170758	chr11:32661954-32661955	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs527847224	chr11:32662032-32662033	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs551109939	chr11:32662117-32662118	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552252066	chr11:32662161-32662162	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs570046186	chr11:32665007-32665008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538695040	chr11:32665015-32665016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376858345	chr11:32665021-32665022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185577755	chr11:32665042-32665043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559001446	chr11:32665059-32665060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114376166	chr11:32665072-32665073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1324397	chr11:32665084-32665085	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs1324398	chr11:32665098-32665099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1324399	chr11:32665128-32665129	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs546409239	chr11:32665176-32665177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574707505	chr11:32665210-32665211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543680903	chr11:32665225-32665226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557264964	chr11:32665239-32665240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564214583	chr11:32665254-32665255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566159011	chr11:32665264-32665265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146830203	chr11:32665360-32665361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565882807	chr11:32674029-32674030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144307184	chr11:32674097-32674098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368305450	chr11:32674098-32674099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568332740	chr11:32674112-32674113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188140163	chr11:32674117-32674118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115596534	chr11:32674131-32674132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114378652	chr11:32674154-32674155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191693267	chr11:32674157-32674158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558587695	chr11:32674161-32674162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572128763	chr11:32674188-32674189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142419791	chr11:32674198-32674199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147952933	chr11:32674224-32674225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372233559	chr11:32674268-32674269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530692519	chr11:32674321-32674322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542840395	chr11:32674379-32674380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537696083	chr11:32674380-32674381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117777755	chr11:32678626-32678627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs80096447	chr11:32678642-32678643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs72910965	chr11:32678656-32678657	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35186796	chr11:32678764-32678765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72910967	chr11:32678784-32678785	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs371398489	chr11:32678814-32678815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144790792	chr11:32678821-32678822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562524639	chr11:32678845-32678846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531572809	chr11:32678887-32678888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147510886	chr11:32678959-32678960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376648802	chr11:32679000-32679001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145650925	chr11:32679200-32679201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573091734	chr11:32679203-32679204	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32665000-32665400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:32674000-32674400	Enhancers	Fetal Lung	lung
3	chr11:32678600-32679000	Enhancers	Fetal Heart	heart
4	chr11:32679200-32680200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:32679600-32680000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:32679600-32680200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:32679600-32681600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:32679600-32681600	Enhancers	HMEC	breast
9	chr11:32679600-32681600	Enhancers	NHEK	skin
10	chr11:32679800-32680200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr11:32679800-32681000	Enhancers	NH-A	brain
12	chr11:32679800-32681600	Enhancers	NHDF-Ad	bronchial
13	chr11:32680000-32680200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr11:32680000-32680800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr11:32680200-32680600	Active TSS	Muscle Satellite Cultured Cells	--
16	chr11:32680200-32680800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:32680200-32681000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:32680200-32681200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:32680200-32681400	Enhancers	A549	lung
20	chr11:32680600-32681000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr11:32680800-32681600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:32681000-32681400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr11:32681000-32682000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:32681200-32681400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr11:32692200-32693000	Enhancers	Rectal Smooth Muscle	rectum
26	chr11:32692600-32693600	Enhancers	Fetal Heart	heart
27	chr11:32693400-32693800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:32708800-32709000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:32711000-32725600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:32714400-32714600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr11:32714400-32714600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr11:32714600-32716400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr11:32716200-32717800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr11:32716400-32717800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr11:32716800-32717800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr11:32717200-32717800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr11:32719800-32720600	Flanking Active TSS	A549	lung
38	chr11:32720000-32720400	Enhancers	HepG2	liver
39	chr11:32720600-32721000	Enhancers	A549	lung
40	chr11:32722800-32724200	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr11:32722800-32724600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:32723000-32723600	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr11:32723000-32723600	Enhancers	Primary hematopoietic stem cells	blood
44	chr11:32723000-32723800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr11:32723200-32723800	Enhancers	Dnd41	blood
46	chr11:32723400-32723800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr11:32723600-32724600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr11:32723800-32725600	Weak transcription	Dnd41	blood
49	chr11:32724600-32724800	Enhancers	Primary hematopoietic stem cells	blood
50	chr11:32725600-32725800	Enhancers	Gastric	stomach

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