Variant report

Variant	nsv469960
Chromosome Location	chr11:56605222-56704042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:780)
CpG islands
(count:244)
Chromatin interactive
region (count:16)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr11:56677375-56678070	A549	lung:	n/a	n/a
2	ATF3	chr11:56615460-56615977	A549	lung:	n/a	n/a
3	ATF3	chr11:56700116-56700807	A549	lung:	n/a	n/a
4	ATF3	chr11:56700056-56700856	A549	lung:	n/a	n/a
5	ATF3	chr11:56674119-56674737	A549	lung:	n/a	n/a
6	ATF3	chr11:56677422-56678255	A549	lung:	n/a	n/a
7	ATF3	chr11:56615453-56615997	A549	lung:	n/a	n/a
8	ATF3	chr11:56700281-56700715	HCT-116	colon:	n/a	n/a
9	BACH1	chr11:56646070-56646184	K562	blood:	n/a	n/a
10	BCL3	chr11:56699810-56701075	A549	lung:	n/a	n/a
11	BCL3	chr11:56677223-56678627	A549	lung:	n/a	chr11:56678412-56678421 chr11:56678413-56678422
12	BCL3	chr11:56615347-56616338	A549	lung:	n/a	n/a
13	BCL3	chr11:56615380-56615997	A549	lung:	n/a	n/a
14	BCL3	chr11:56677385-56678346	A549	lung:	n/a	n/a
15	BCL3	chr11:56673973-56674803	A549	lung:	n/a	n/a
16	BCL3	chr11:56673648-56674760	A549	lung:	n/a	n/a
17	BCL3	chr11:56700090-56700807	A549	lung:	n/a	n/a
18	CBX3	chr11:56700195-56700768	HCT-116	colon:	n/a	n/a
19	CEBPB	chr11:56700226-56700811	HCT-116	colon:	n/a	n/a
20	CEBPB	chr11:56692200-56692499	A549	lung:	n/a	chr11:56692374-56692386 chr11:56692343-56692354
21	CEBPB	chr11:56677145-56679193	A549	lung:	n/a	chr11:56677154-56677166
22	CEBPB	chr11:56699438-56699655	A549	lung:	n/a	chr11:56699596-56699607
23	CEBPB	chr11:56681837-56681985	HepG2	liver:	n/a	chr11:56681902-56681913 chr11:56681904-56681913 chr11:56681903-56681914
24	CEBPB	chr11:56692208-56692478	HepG2	liver:	n/a	chr11:56692374-56692386 chr11:56692343-56692354
25	CEBPB	chr11:56693584-56693847	HepG2	liver:	n/a	chr11:56693693-56693704 chr11:56693692-56693703 chr11:56693692-56693705
26	CEBPB	chr11:56644885-56645198	HepG2	liver:	n/a	chr11:56645019-56645030
27	CEBPB	chr11:56700358-56700682	IMR90	lung:	n/a	n/a
28	CEBPB	chr11:56664891-56665471	HepG2	liver:	n/a	chr11:56665031-56665042
29	CEBPB	chr11:56608674-56609010	A549	lung:	n/a	n/a
30	CEBPB	chr11:56653864-56654402	A549	lung:	n/a	chr11:56654140-56654153
31	CEBPB	chr11:56693610-56693866	A549	lung:	n/a	chr11:56693693-56693704 chr11:56693692-56693703 chr11:56693692-56693705
32	CEBPB	chr11:56653963-56654311	A549	lung:	n/a	chr11:56654140-56654153
33	CEBPB	chr11:56615462-56616086	A549	lung:	n/a	n/a
34	CEBPB	chr11:56692190-56692508	Hela-S3	cervix:	n/a	chr11:56692374-56692386 chr11:56692343-56692354
35	CEBPB	chr11:56672207-56672605	A549	lung:	n/a	chr11:56672486-56672499 chr11:56672488-56672499 chr11:56672488-56672499
36	CEBPB	chr11:56700263-56700810	HCT-116	colon:	n/a	n/a
37	CEBPB	chr11:56653973-56654278	HepG2	liver:	n/a	chr11:56654140-56654153
38	CEBPB	chr11:56616784-56617073	A549	lung:	n/a	n/a
39	CEBPB	chr11:56672226-56672606	HepG2	liver:	n/a	chr11:56672486-56672499 chr11:56672488-56672499 chr11:56672488-56672499
40	CEBPB	chr11:56677430-56678043	A549	lung:	n/a	n/a
41	CEBPB	chr11:56643958-56644540	A549	lung:	n/a	n/a
42	CEBPB	chr11:56699986-56701097	A549	lung:	n/a	n/a
43	CEBPB	chr11:56617279-56617787	A549	lung:	n/a	chr11:56617512-56617523
44	CEBPB	chr11:56677062-56678333	A549	lung:	n/a	chr11:56677154-56677166
45	CEBPB	chr11:56699562-56699629	HepG2	liver:	n/a	chr11:56699596-56699607
46	CEBPB	chr11:56674000-56675226	A549	lung:	n/a	n/a
47	CEBPB	chr11:56675074-56675163	A549	lung:	n/a	n/a
48	CEBPB	chr11:56644882-56645189	IMR90	lung:	n/a	chr11:56645019-56645030
49	CEBPB	chr11:56666303-56666724	A549	lung:	n/a	n/a
50	CEBPB	chr11:56617323-56617647	A549	lung:	n/a	chr11:56617512-56617523

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56643145-56643195	GM19239	blood:	n/a
2	chr11:56615879-56615929	ovcar-3	ovarian:	n/a
3	chr11:56615879-56615929	AG09319	gingival:	n/a
4	chr11:56643145-56643195	PrEC	prostate:	n/a
5	chr11:56615879-56615929	HRPEpiC	eye:	n/a
6	chr11:56615725-56615775	SK-N-SH	brain:	n/a
7	chr11:56614928-56614978	PrEC	prostate:	n/a
8	chr11:56643145-56643195	PFSK-1	brain:	n/a
9	chr11:56615879-56615929	HepG2	liver:	n/a
10	chr11:56615879-56615929	A549	lung:	n/a
11	chr11:56643145-56643195	SK-N-MC	brain:	n/a
12	chr11:56615879-56615929	NHDF-neo	bronchial:	n/a
13	chr11:56615725-56615775	NH-A	brain:	n/a
14	chr11:56615879-56615929	AG04450	lung:	fetal
15	chr11:56615725-56615775	CMK	blood:	n/a
16	chr11:56643145-56643195	H1-hESC	embryonic stem cell:	embryo
17	chr11:56615879-56615929	AG10803	skin:	n/a
18	chr11:56643145-56643195	HRPEpiC	eye:	n/a
19	chr11:56615725-56615775	HepG2	liver:	n/a
20	chr11:56614928-56614978	Hela-S3	cervix:	n/a
21	chr11:56643145-56643195	T-47D	breast:	n/a
22	chr11:56615725-56615775	HRCEpiC	kidney:	n/a
23	chr11:56614928-56614978	SK-N-SH	brain:	n/a
24	chr11:56614928-56614978	HL-60	blood:	n/a
25	chr11:56615725-56615775	ovcar-3	ovarian:	n/a
26	chr11:56643145-56643195	GM06990	blood:	n/a
27	chr11:56615879-56615929	PANC-1	pancreas:	n/a
28	chr11:56615725-56615775	NT2-D1	testis:	n/a
29	chr11:56643145-56643195	ProgFib	skin:	n/a
30	chr11:56614928-56614978	HRPEpiC	eye:	n/a
31	chr11:56615879-56615929	SK-N-MC	brain:	n/a
32	chr11:56614928-56614978	GM12892	blood:	n/a
33	chr11:56614928-56614978	HEEpiC	esophagus:	n/a
34	chr11:56614928-56614978	Hepatocyte	liver:	n/a
35	chr11:56615725-56615775	K562	blood:	n/a
36	chr11:56643145-56643195	HEEpiC	esophagus:	n/a
37	chr11:56615879-56615929	HCPEpiC	choroid plexus:	n/a
38	chr11:56614928-56614978	HRE	kidney:	n/a
39	chr11:56615725-56615775	AG09309	skin:	n/a
40	chr11:56615879-56615929	GM19239	blood:	n/a
41	chr11:56615725-56615775	SK-N-SH_RA	brain:	n/a
42	chr11:56643145-56643195	ovcar-3	ovarian:	n/a
43	chr11:56615879-56615929	HRCEpiC	kidney:	n/a
44	chr11:56615879-56615929	HCT-116	colon:	n/a
45	chr11:56615725-56615775	AG09319	gingival:	n/a
46	chr11:56615879-56615929	AG04449	skin:	fetal
47	chr11:56643145-56643195	MCF-7	breast:	n/a
48	chr11:56643145-56643195	AoSMC	blood vessel:	n/a
49	chr11:56614928-56614978	AG10803	skin:	n/a
50	chr11:56615879-56615929	HUVEC	blood vessel:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:56646465..56649384-chr11:56653182..56655132,3	K562	blood:
2	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:
3	chr11:56608383..56609306-chr11:57016176..57017128,2	MCF-7	breast:
4	chr11:56664007..56666719-chr11:56666908..56669064,2	K562	blood:
5	chr11:56618059..56620569-chr11:56629242..56631002,2	K562	blood:
6	chr11:56628427..56630548-chr11:56631596..56633931,2	K562	blood:
7	chr11:56604071..56605908-chr11:56606591..56609227,2	K562	blood:
8	chr11:56608476..56609545-chr11:57016926..57017835,4	K562	blood:
9	chr11:56628427..56630548-chr11:56631596..56633931,2	K562	blood:
10	chr11:56608365..56609372-chr11:57017133..57018075,3	MCF-7	breast:
11	chr11:56604071..56605908-chr11:56606591..56609227,2	K562	blood:
12	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:
13	chr11:56664007..56666719-chr11:56666908..56669064,2	K562	blood:
14	chr11:56646465..56649384-chr11:56653182..56655132,3	K562	blood:
15	chr11:56608400..56609354-chr11:57016455..57017401,5	MCF-7	breast:
16	chr11:56618059..56620569-chr11:56629242..56631002,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR5AK2-1	chr11:56615954-56616091	ENSG00000255433
2	lnc-OR5AK2-1	chr11:56642200-56642319	NR_110136
3	lnc-OR5AK2-1	chr11:56615954-56616091	NR_110136
4	lnc-OR5AK2-1	chr11:56643073-56645554	NR_110136
5	lnc-OR5AK2-1	chr11:56615954-56616091	XLOC_009132
6	lnc-OR5AK2-1	chr11:56643073-56644687	ENSG00000255433
7	lnc-OR5AK2-1	chr11:56642200-56642319	ENSG00000255433
8	lnc-OR5AK2-1	chr11:56638567-56638727	NR_110136
9	lnc-OR5AK2-1	chr11:56643073-56645554	ENSG00000255433
10	lnc-OR5AK2-1	chr11:56638567-56638727	XLOC_009132
11	lnc-OR5AK2-1	chr11:56616044-56616091	ENSG00000255433
12	lnc-OR5AK2-1	chr11:56643073-56645554	XLOC_009132
13	lnc-OR5AK2-1	chr11:56638567-56638727	ENSG00000255433
14	lnc-OR5AK2-1	chr11:56638567-56638727	ENSG00000255433

No data

Variant related genes	Relation type
ENSG00000255433	TF binding region
ENSG00000255433	CpG island

Extended variants
information (count: 3833 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3833 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573908748	chr11:56607604-56607605	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs144215184	chr11:56607630-56607631	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs181688140	chr11:56607636-56607637	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs56915444	chr11:56607641-56607642	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs1792515	chr11:56607654-56607655	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs185493293	chr11:56607708-56607709	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs76912979	chr11:56607725-56607726	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs546862947	chr11:56607743-56607744	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs369088133	chr11:56607872-56607873	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs373822407	chr11:56607873-56607874	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs568320845	chr11:56607910-56607911	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs61889065	chr11:56607915-56607916	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs117885677	chr11:56607967-56607968	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs568987600	chr11:56608021-56608022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539502116	chr11:56608034-56608035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74445330	chr11:56608050-56608051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566455362	chr11:56608062-56608063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202062388	chr11:56608124-56608125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs60240751	chr11:56608152-56608153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556031731	chr11:56608202-56608203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538318928	chr11:56608297-56608298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561802275	chr11:56608346-56608347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59496802	chr11:56608353-56608354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs568890224	chr11:56608360-56608361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189921956	chr11:56608367-56608368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577741277	chr11:56608453-56608454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146330090	chr11:56608495-56608496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559264634	chr11:56608525-56608526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537448136	chr11:56608532-56608533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569458950	chr11:56608602-56608603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199879368	chr11:56608623-56608624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560325530	chr11:56608662-56608663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139704688	chr11:56608674-56608675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs652689	chr11:56608758-56608759	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs182270299	chr11:56608760-56608761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545462482	chr11:56608776-56608777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186536476	chr11:56608782-56608783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377550155	chr11:56608785-56608786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550827213	chr11:56608803-56608804	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs190713962	chr11:56608856-56608857	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs146641957	chr11:56608857-56608858	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs368388819	chr11:56608891-56608892	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs540141523	chr11:56608893-56608894	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs551466980	chr11:56608926-56608927	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs553658573	chr11:56608960-56608961	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs566401050	chr11:56608984-56608985	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs72912543	chr11:56608998-56608999	Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs372434777	chr11:56609091-56609092	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs12360757	chr11:56609115-56609116	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs12808001	chr11:56609145-56609146	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:53)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Breast cancer	17142309	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56607600-56608000	ZNF genes & repeats	A549	lung
2	chr11:56608000-56608600	Weak transcription	A549	lung
3	chr11:56608600-56609000	Enhancers	A549	lung
4	chr11:56608800-56609000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
5	chr11:56608800-56609200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr11:56608800-56609200	Enhancers	Liver	Liver
7	chr11:56608800-56609200	Enhancers	Fetal Kidney	kidney
8	chr11:56608800-56610200	Enhancers	HMEC	breast
9	chr11:56609000-56609200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:56609000-56609200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:56609000-56609200	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
12	chr11:56609000-56609200	Flanking Active TSS	Brain Hippocampus Middle	brain
13	chr11:56609000-56609200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr11:56609000-56609200	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr11:56609000-56609200	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr11:56609000-56609400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:56609000-56609400	Enhancers	Fetal Brain Male	brain
18	chr11:56609000-56609400	Flanking Active TSS	A549	lung
19	chr11:56609000-56609400	Enhancers	NHEK	skin
20	chr11:56609000-56609800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr11:56609000-56609800	Enhancers	Fetal Intestine Large	intestine
22	chr11:56609000-56610800	Enhancers	Fetal Lung	lung
23	chr11:56609000-56611000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr11:56609000-56611600	Enhancers	Stomach Mucosa	stomach
25	chr11:56609200-56610000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:56609200-56613800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:56609200-56614000	Weak transcription	Fetal Kidney	kidney
28	chr11:56609400-56610800	Enhancers	A549	lung
29	chr11:56609400-56613800	Weak transcription	NHEK	skin
30	chr11:56609800-56610800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:56610200-56613600	Weak transcription	HMEC	breast
32	chr11:56610800-56611600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:56610800-56613200	ZNF genes & repeats	A549	lung
34	chr11:56610800-56614400	Weak transcription	Fetal Lung	lung
35	chr11:56611000-56612800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:56611600-56613800	Weak transcription	Stomach Mucosa	stomach
37	chr11:56611600-56614000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:56612400-56613200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr11:56612400-56613200	Enhancers	Lung	lung
40	chr11:56612800-56613200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr11:56613200-56613600	Weak transcription	Lung	lung
42	chr11:56613200-56613800	Weak transcription	A549	lung
43	chr11:56613200-56614000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:56613200-56618400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:56613600-56614800	Enhancers	Lung	lung
46	chr11:56613600-56617800	Enhancers	HMEC	breast
47	chr11:56613800-56614400	Enhancers	Stomach Mucosa	stomach
48	chr11:56613800-56614600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr11:56613800-56614800	Enhancers	NHEK	skin
50	chr11:56613800-56615000	Enhancers	A549	lung

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