Variant report

Variant	nsv897312
Chromosome Location	chr11:45663568-45699134
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:653)
CpG islands
(count:1769)
Chromatin interactive
region (count:18)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:653 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45684629-45684635	K562	blood:	n/a	n/a
2	ARID3A	chr11:45676873-45677048	K562	blood:	n/a	n/a
3	ATF2	chr11:45698004-45698493	GM12878	blood:	n/a	n/a
4	ATF3	chr11:45668146-45668434	GM12878	blood:	n/a	n/a
5	ATF3	chr11:45668072-45668501	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr11:45668101-45668510	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr11:45668185-45668458	K562	blood:	n/a	n/a
8	ATF3	chr11:45676850-45677177	K562	blood:	n/a	n/a
9	ATF3	chr11:45676830-45677081	K562	blood:	n/a	n/a
10	BACH1	chr11:45676782-45677123	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:45684470-45684843	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr11:45698033-45698498	GM12878	blood:	n/a	n/a
13	BATF	chr11:45696801-45697089	GM12878	blood:	n/a	chr11:45696983-45696993 chr11:45696982-45696993
14	BATF	chr11:45698057-45698468	GM12878	blood:	n/a	n/a
15	BCL11A	chr11:45698052-45698469	GM12878	blood:	n/a	n/a
16	BCL11A	chr11:45698110-45698413	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:45676951-45677124	GM12878	blood:	n/a	n/a
18	BHLHE40	chr11:45676651-45677055	K562	blood:	n/a	n/a
19	BHLHE40	chr11:45674503-45674754	K562	blood:	n/a	n/a
20	BHLHE40	chr11:45671164-45671382	K562	blood:	n/a	n/a
21	BRCA1	chr11:45664562-45664572	GM12878	blood:	n/a	n/a
22	BRCA1	chr11:45676938-45677048	HepG2	liver:	n/a	n/a
23	BRCA1	chr11:45676882-45677132	H1-hESC	embryonic stem cell:	n/a	n/a
24	CCNT2	chr11:45671111-45671406	K562	blood:	n/a	n/a
25	CEBPB	chr11:45676892-45677278	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:45676906-45677182	A549	lung:	n/a	n/a
27	CEBPB	chr11:45676840-45677234	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:45676862-45677340	MCF-7	breast:	n/a	n/a
29	CEBPB	chr11:45676942-45677240	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:45668245-45668365	K562	blood:	n/a	n/a
31	CEBPB	chr11:45676937-45677275	K562	blood:	n/a	n/a
32	CHD1	chr11:45686332-45686365	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr11:45674129-45674205	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr11:45676856-45677115	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr11:45668101-45668492	K562	blood:	n/a	n/a
36	CHD2	chr11:45671167-45671200	K562	blood:	n/a	n/a
37	CHD2	chr11:45676839-45677097	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr11:45677074-45677201	HepG2	liver:	n/a	n/a
39	CHD2	chr11:45676842-45677029	K562	blood:	n/a	n/a
40	CHD2	chr11:45668190-45668506	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr11:45676801-45677320	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr11:45676697-45677340	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr11:45676782-45677174	A549	lung:	n/a	n/a
44	CTCF	chr11:45693520-45693670	K562	blood:	n/a	chr11:45693595-45693608
45	CTCF	chr11:45676920-45677070	GM12801	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
46	CTCF	chr11:45676940-45677090	HepG2	liver:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
47	CTCF	chr11:45676940-45677090	HCT-116	colon:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
48	CTCF	chr11:45680280-45680430	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr11:45676920-45677070	HL-60	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
50	CTCF	chr11:45676920-45677070	HUVEC	blood vessel:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45686055-45686105	HL-60	blood:	n/a
2	chr11:45689077-45689127	ECC-1	luminal epithelium:	n/a
3	chr11:45683401-45683451	SAEC	small airway:	n/a
4	chr11:45687281-45687331	HAEpiC	amniotic membrane:	n/a
5	chr11:45687319-45687369	HEEpiC	esophagus:	n/a
6	chr11:45687319-45687369	PrEC	prostate:	n/a
7	chr11:45687263-45687313	HepG2	liver:	n/a
8	chr11:45687277-45687327	PFSK-1	brain:	n/a
9	chr11:45672536-45672586	SK-N-MC	brain:	n/a
10	chr11:45671015-45671065	NH-A	brain:	n/a
11	chr11:45673410-45673460	NH-A	brain:	n/a
12	chr11:45698622-45698672	HCPEpiC	choroid plexus:	n/a
13	chr11:45672555-45672605	HCM	heart:	n/a
14	chr11:45683401-45683451	HCPEpiC	choroid plexus:	n/a
15	chr11:45687443-45687493	MCF10A-Er-Src	breast:	n/a
16	chr11:45671015-45671065	AG09309	skin:	n/a
17	chr11:45672100-45672150	HCT-116	colon:	n/a
18	chr11:45687319-45687369	GM12891	blood:	n/a
19	chr11:45674702-45674752	HL-60	blood:	n/a
20	chr11:45688659-45688709	Hela-S3	cervix:	n/a
21	chr11:45672756-45672806	U87	brain:	n/a
22	chr11:45687277-45687327	AG09319	gingival:	n/a
23	chr11:45672555-45672605	PFSK-1	brain:	n/a
24	chr11:45686055-45686105	CMK	blood:	n/a
25	chr11:45697908-45697958	SK-N-SH_RA	brain:	n/a
26	chr11:45687443-45687493	SKMC	muscle:	n/a
27	chr11:45687494-45687544	HAEpiC	amniotic membrane:	n/a
28	chr11:45672536-45672586	HL-60	blood:	n/a
29	chr11:45697908-45697958	CMK	blood:	n/a
30	chr11:45674702-45674752	HUVEC	blood vessel:	n/a
31	chr11:45690461-45690511	NB4	blood:	n/a
32	chr11:45673410-45673460	HMEC	breast:	n/a
33	chr11:45687275-45687325	SK-N-SH_RA	brain:	n/a
34	chr11:45672100-45672150	SAEC	small airway:	n/a
35	chr11:45672756-45672806	AG04450	lung:	fetal
36	chr11:45674238-45674288	HepG2	liver:	n/a
37	chr11:45672529-45672579	NH-A	brain:	n/a
38	chr11:45683401-45683451	RPTEC	kidney:	n/a
39	chr11:45686055-45686105	HCT-116	colon:	n/a
40	chr11:45671015-45671065	LNCaP	prostate:	n/a
41	chr11:45687281-45687331	HRPEpiC	eye:	n/a
42	chr11:45687281-45687331	LNCaP	prostate:	n/a
43	chr11:45687055-45687105	HRE	kidney:	n/a
44	chr11:45671369-45671419	CMK	blood:	n/a
45	chr11:45687319-45687369	MCF-7	breast:	n/a
46	chr11:45688659-45688709	MCF10A-Er-Src	breast:	n/a
47	chr11:45687890-45687940	AG10803	skin:	n/a
48	chr11:45672536-45672586	HepG2	liver:	n/a
49	chr11:45689077-45689127	ProgFib	skin:	n/a
50	chr11:45687890-45687940	HNPCEpiC	eye:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:45658659..45661256-chr11:45675243..45676992,2	K562	blood:
2	chr11:45678783..45681662-chr11:45685006..45688205,4	MCF-7	breast:
3	chr11:45672171..45675080-chr11:45682496..45685022,2	K562	blood:
4	chr11:45673604..45675879-chr11:45677397..45678906,2	K562	blood:
5	chr11:45427814..45428397-chr11:45676543..45677286,2	MCF-7	breast:
6	chr11:45659181..45661642-chr11:45665618..45668117,2	K562	blood:
7	chr11:45690995..45692950-chr11:45699532..45701438,2	MCF-7	breast:
8	chr11:45673604..45675879-chr11:45677397..45678906,2	K562	blood:
9	chr11:45686097..45689111-chr11:45690987..45693676,3	MCF-7	breast:
10	chr11:45671225..45673031-chr11:45675062..45677985,2	K562	blood:
11	chr11:45693262..45695561-chr11:45696192..45697922,2	K562	blood:
12	chr11:45671225..45673031-chr11:45675062..45677985,2	K562	blood:
13	chr11:45392488..45393362-chr11:45676466..45677098,3	MCF-7	breast:
14	chr11:45673703..45676177-chr11:45681263..45683293,2	K562	blood:
15	chr11:45676348..45677919-chr11:45792905..45794177,5	K562	blood:
16	chr11:45677224..45679884-chr11:45774991..45777658,2	MCF-7	breast:
17	chr11:45673703..45676177-chr11:45681263..45683293,2	K562	blood:
18	chr11:45693262..45695561-chr11:45696192..45697922,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf94-5	chr11:45686728-45687144	NONHSAT019041
2	lnc-CTD-2210P24.4.1-8	chr11:45693469-45700657	l_471_chr11:45693468-45701603_testes
3	lnc-CTD-2210P24.4.1-2	chr11:45674019-45674355	NONHSAT019042
4	lnc-C11orf94-6	chr11:45670429-45670640	NONHSAT019040
5	lnc-C11orf94-5	chr11:45672783-45673640	NONHSAT019041
6	lnc-C11orf94-6	chr11:45670881-45671184	NONHSAT019040
7	lnc-C11orf94-5	chr11:45674071-45674156	NONHSAT019041
8	lnc-CTD-2210P24.4.1-2	chr11:45674019-45674241	ENSG00000255091.1
9	lnc-CTD-2210P24.4.1-2	chr11:45673079-45673104	ENSG00000255091.1
10	lnc-CTD-2210P24.4.1-2	chr11:45672876-45673104	NONHSAT019042

No data

Variant related genes	Relation type
ENSG00000255091	TF binding region
CHST1	TF binding region
ENSG00000255091	CpG island
CHST1	CpG island
ENSG00000255091	chromatin interactions
ENSG00000255267	chromatin interactions
ENSG00000175264	chromatin interactions
ENSG00000205106	chromatin interactions

Extended variants
information (count: 1358 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1348965	chr11:45663568-45663569	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72896772	chr11:45663592-45663593	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs540049647	chr11:45663596-45663597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556535310	chr11:45663611-45663612	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs142298011	chr11:45663618-45663619	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs539656298	chr11:45663632-45663633	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs193209338	chr11:45663644-45663645	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs145971443	chr11:45663653-45663654	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs535343351	chr11:45663680-45663681	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs555808122	chr11:45663715-45663716	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs114008360	chr11:45663738-45663739	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs576684713	chr11:45663759-45663760	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs541812287	chr11:45663769-45663770	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs368844880	chr11:45663855-45663856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534993786	chr11:45663871-45663872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555390804	chr11:45663874-45663875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371474234	chr11:45663895-45663896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558317377	chr11:45663926-45663927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139892415	chr11:45663944-45663945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375006989	chr11:45663953-45663954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544041550	chr11:45663979-45663980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142104184	chr11:45663992-45663993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183481005	chr11:45664014-45664015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542876665	chr11:45664024-45664025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114617719	chr11:45664030-45664031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527318471	chr11:45664070-45664071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546976250	chr11:45664110-45664111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374904160	chr11:45664124-45664125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74900639	chr11:45664133-45664134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35613675	chr11:45664137-45664138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139847528	chr11:45664191-45664192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532180290	chr11:45664207-45664208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187261674	chr11:45664215-45664216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191773499	chr11:45664222-45664223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554226004	chr11:45664226-45664227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549272722	chr11:45664261-45664262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565963916	chr11:45664284-45664285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150290488	chr11:45664325-45664326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115300023	chr11:45664326-45664327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184095390	chr11:45664341-45664342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs35323479	chr11:45664348-45664349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116281512	chr11:45664367-45664368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs578052013	chr11:45664451-45664452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75715129	chr11:45664464-45664465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1992849	chr11:45664488-45664489	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs188483897	chr11:45664522-45664523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192482271	chr11:45664537-45664538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548203313	chr11:45664557-45664558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117308978	chr11:45664570-45664571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs60550474	chr11:45664586-45664587	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1061 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45659200-45669400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:45663000-45666800	Enhancers	HUVEC	blood vessel
3	chr11:45663400-45663600	Enhancers	Spleen	Spleen
4	chr11:45663400-45666200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr11:45663600-45663800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:45663600-45663800	Enhancers	Left Ventricle	heart
7	chr11:45663600-45664200	Enhancers	Lung	lung
8	chr11:45663600-45671200	Weak transcription	Spleen	Spleen
9	chr11:45663800-45664000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr11:45664200-45665200	Weak transcription	Lung	lung
11	chr11:45664600-45665800	Enhancers	NHEK	skin
12	chr11:45664800-45665000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr11:45664800-45665600	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr11:45664800-45665800	Enhancers	Left Ventricle	heart
15	chr11:45664800-45665800	Enhancers	Right Ventricle	heart
16	chr11:45665000-45665600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:45665000-45665800	Enhancers	Fetal Brain Female	brain
18	chr11:45665200-45665400	Weak transcription	Gastric	stomach
19	chr11:45665200-45665600	Enhancers	HMEC	breast
20	chr11:45665200-45665800	Enhancers	Lung	lung
21	chr11:45665400-45665600	Enhancers	Fetal Muscle Leg	muscle
22	chr11:45665400-45665600	Enhancers	Gastric	stomach
23	chr11:45665400-45665800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr11:45665400-45665800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr11:45665600-45665800	Enhancers	Brain Anterior Caudate	brain
26	chr11:45665600-45667600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:45665600-45671000	Weak transcription	Fetal Muscle Leg	muscle
28	chr11:45665600-45674400	Weak transcription	HMEC	breast
29	chr11:45665600-45680000	Weak transcription	Gastric	stomach
30	chr11:45665800-45666800	Weak transcription	Lung	lung
31	chr11:45665800-45667800	Weak transcription	NHEK	skin
32	chr11:45665800-45669400	Weak transcription	Left Ventricle	heart
33	chr11:45665800-45670600	Weak transcription	Fetal Brain Female	brain
34	chr11:45665800-45670600	Weak transcription	Right Ventricle	heart
35	chr11:45665800-45671200	Weak transcription	Brain Anterior Caudate	brain
36	chr11:45665800-45671800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr11:45666200-45671000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:45666800-45667400	Weak transcription	HUVEC	blood vessel
39	chr11:45667400-45669800	Enhancers	HUVEC	blood vessel
40	chr11:45667800-45668000	Enhancers	NHEK	skin
41	chr11:45667800-45668200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
42	chr11:45667800-45670600	Weak transcription	Aorta	Aorta
43	chr11:45668000-45668200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:45668000-45668200	Flanking Active TSS	NHEK	skin
45	chr11:45668600-45670600	Weak transcription	Ovary	ovary
46	chr11:45668600-45671200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr11:45668800-45669400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:45668800-45670200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr11:45669000-45669800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr11:45669000-45669800	Enhancers	Adipose Nuclei	Adipose

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