Variant report

Variant	nsv896989
Chromosome Location	chr11:9951968-10059623
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:926)
CpG islands
(count:245)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:9972006-9972363	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:9954531-9954676	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:9952406-9952773	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:10012155-10012488	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:10043130-10043553	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:10043290-10043511	K562	blood:	n/a	n/a
7	ATF1	chr11:10043170-10043518	K562	blood:	n/a	n/a
8	ATF1	chr11:9952454-9952810	K562	blood:	n/a	n/a
9	ATF1	chr11:9978223-9978390	K562	blood:	n/a	n/a
10	ATF2	chr11:9984169-9984650	GM12878	blood:	n/a	n/a
11	ATF2	chr11:9984115-9984704	GM12878	blood:	n/a	n/a
12	ATF3	chr11:10004659-10005096	A549	lung:	n/a	n/a
13	BACH1	chr11:10048428-10048444	K562	blood:	n/a	n/a
14	BATF	chr11:9994519-9994792	GM12878	blood:	n/a	chr11:9994688-9994697
15	BATF	chr11:9984302-9984676	GM12878	blood:	n/a	n/a
16	BATF	chr11:9969025-9969393	GM12878	blood:	n/a	n/a
17	BCL3	chr11:10004548-10005126	A549	lung:	n/a	n/a
18	BCL3	chr11:10004437-10005076	A549	lung:	n/a	n/a
19	BCLAF1	chr11:9984271-9984598	GM12878	blood:	n/a	n/a
20	BCLAF1	chr11:9984166-9984674	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:9984365-9984604	GM12878	blood:	n/a	n/a
22	BRCA1	chr11:9994495-9994970	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr11:10004722-10005080	K562	blood:	n/a	n/a
24	CEBPB	chr11:9978058-9978263	IMR90	lung:	n/a	chr11:9978174-9978185
25	CEBPB	chr11:10051761-10051913	IMR90	lung:	n/a	n/a
26	CEBPB	chr11:9964979-9965792	IMR90	lung:	n/a	n/a
27	CEBPB	chr11:9952541-9952703	K562	blood:	n/a	n/a
28	CEBPB	chr11:9952438-9952795	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:9965293-9965650	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:9965257-9965685	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:9994600-9994759	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr11:9965150-9965713	A549	lung:	n/a	n/a
33	CEBPB	chr11:10051802-10051905	K562	blood:	n/a	n/a
34	CEBPB	chr11:9965344-9965688	A549	lung:	n/a	n/a
35	CEBPB	chr11:9978063-9978347	K562	blood:	n/a	chr11:9978174-9978185
36	CEBPB	chr11:9965223-9965725	A549	lung:	n/a	n/a
37	CEBPB	chr11:9990638-9990986	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr11:9954472-9954738	HepG2	liver:	n/a	chr11:9954537-9954548
39	CEBPB	chr11:9978076-9978275	K562	blood:	n/a	chr11:9978174-9978185
40	CEBPB	chr11:9952475-9952674	HepG2	liver:	n/a	n/a
41	CHD2	chr11:9952440-9952769	HepG2	liver:	n/a	n/a
42	CHD2	chr11:9994597-9994793	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr11:9952562-9952631	K562	blood:	n/a	n/a
44	CREB1	chr11:10004678-10005094	A549	lung:	n/a	n/a
45	CTCF	chr11:9994515-9994742	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr11:9995780-9995930	A549	lung:	n/a	n/a
47	CTCF	chr11:9995800-9995950	GM12873	blood:	n/a	n/a
48	CTCF	chr11:9994413-9994824	IMR90	lung:	n/a	n/a
49	CTCF	chr11:9994560-9994710	GM12875	blood:	n/a	n/a
50	CTCF	chr11:9994500-9994650	MCF-7	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10051398-10051448	NT2-D1	testis:	n/a
2	chr11:10051398-10051448	NT2-D1	testis:	n/a
3	chr11:9992187-9992237	GM06990	blood:	n/a
4	chr11:9995602-9995652	Jurkat	blood:	n/a
5	chr11:10051398-10051448	PrEC	prostate:	n/a
6	chr11:9995602-9995652	GM12891	blood:	n/a
7	chr11:10002835-10002885	ProgFib	skin:	n/a
8	chr11:9992187-9992237	SAEC	small airway:	n/a
9	chr11:10002835-10002885	HEK293	kidney:	embryo
10	chr11:10002835-10002885	PFSK-1	brain:	n/a
11	chr11:10051398-10051448	PANC-1	pancreas:	n/a
12	chr11:10051398-10051448	AoSMC	blood vessel:	n/a
13	chr11:10051398-10051448	MCF10A-Er-Src	breast:	n/a
14	chr11:9995602-9995652	LNCaP	prostate:	n/a
15	chr11:9992187-9992237	Caco-2	colon:	n/a
16	chr11:10002835-10002885	SKMC	muscle:	n/a
17	chr11:9995602-9995652	SAEC	small airway:	n/a
18	chr11:10051398-10051448	GM19239	blood:	n/a
19	chr11:9995602-9995652	SK-N-SH	brain:	n/a
20	chr11:10002835-10002885	HAEpiC	amniotic membrane:	n/a
21	chr11:9995602-9995652	HRCEpiC	kidney:	n/a
22	chr11:9995602-9995652	HAEpiC	amniotic membrane:	n/a
23	chr11:9992187-9992237	SK-N-MC	brain:	n/a
24	chr11:9995602-9995652	A549	lung:	n/a
25	chr11:10051398-10051448	U87	brain:	n/a
26	chr11:10002835-10002885	ECC-1	luminal epithelium:	n/a
27	chr11:9992187-9992237	HNPCEpiC	eye:	n/a
28	chr11:10002835-10002885	NT2-D1	testis:	n/a
29	chr11:10051398-10051448	NH-A	brain:	n/a
30	chr11:10002835-10002885	AG04449	skin:	fetal
31	chr11:9995602-9995652	HCM	heart:	n/a
32	chr11:10002835-10002885	ovcar-3	ovarian:	n/a
33	chr11:10051398-10051448	HEK293	kidney:	embryo
34	chr11:10002835-10002885	H1-hESC	embryonic stem cell:	embryo
35	chr11:10002835-10002885	HCT-116	colon:	n/a
36	chr11:10051398-10051448	AG10803	skin:	n/a
37	chr11:9995602-9995652	HepG2	liver:	n/a
38	chr11:9992187-9992237	AoSMC	blood vessel:	n/a
39	chr11:10051398-10051448	Hela-S3	cervix:	n/a
40	chr11:9992187-9992237	AG10803	skin:	n/a
41	chr11:9995602-9995652	NB4	blood:	n/a
42	chr11:10051398-10051448	GM12891	blood:	n/a
43	chr11:9992187-9992237	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:9992187-9992237	AG04449	skin:	fetal
45	chr11:9992187-9992237	BJ	skin:	n/a
46	chr11:9995602-9995652	HNPCEpiC	eye:	n/a
47	chr11:9992187-9992237	HCT-116	colon:	n/a
48	chr11:9995602-9995652	HCF	heart:	n/a
49	chr11:9992187-9992237	HepG2	liver:	n/a
50	chr11:10002835-10002885	PANC-1	pancreas:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:9883380..9884276-chr11:9994232..9995105,4	MCF-7	breast:
2	chr11:9967314..9969682-chr11:9973855..9976394,2	MCF-7	breast:
3	chr11:9991428..9993143-chr11:10058135..10060614,2	K562	blood:
4	chr11:10051045..10052894-chr11:10053055..10055381,2	MCF-7	breast:
5	chr11:10012620..10013540-chr11:10329095..10329739,2	MCF-7	breast:
6	chr11:10000703..10003036-chr11:10327811..10330632,2	MCF-7	breast:
7	chr11:9994901..9996412-chr11:10324131..10325757,2	MCF-7	breast:
8	chr11:9967314..9969682-chr11:9973855..9976394,2	MCF-7	breast:
9	chr11:9482450..9484248-chr11:9984519..9986171,2	K562	blood:
10	chr11:10002720..10004321-chr11:10011527..10014066,2	K562	blood:
11	chr11:9883445..9884416-chr11:9994096..9994928,3	MCF-7	breast:
12	chr11:10004750..10006557-chr11:10010668..10012877,2	MCF-7	breast:
13	chr11:9991428..9993143-chr11:10058135..10060614,2	K562	blood:
14	chr11:10051045..10052894-chr11:10053055..10055381,2	MCF-7	breast:
15	chr11:9994842..9997807-chr11:10313418..10316499,3	MCF-7	breast:
16	chr11:10011394..10012992-chr11:10327878..10330326,2	MCF-7	breast:
17	chr11:10004750..10006557-chr11:10010668..10012877,2	MCF-7	breast:
18	chr11:10010659..10013525-chr11:10017615..10019134,2	K562	blood:
19	chr11:10002720..10004321-chr11:10011527..10014066,2	K562	blood:
20	chr11:10010659..10013525-chr11:10017615..10019134,2	K562	blood:
21	chr11:10012021..10012653-chr11:10098365..10099087,2	MCF-7	breast:
22	chr11:9779414..9780281-chr11:9994114..9995162,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254765	TF binding region
SBF2	TF binding region
ENSG00000254765	CpG island
SBF2	CpG island
ENSG00000246273	chromatin interactions
ENSG00000245522	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000254554	chromatin interactions
ENSG00000133812	chromatin interactions
ENSG00000166478	chromatin interactions

Extended variants
information (count: 4469 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4469 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10840327	chr11:9951968-9951969	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572029356	chr11:9951987-9951988	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540199999	chr11:9952029-9952030	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs368996739	chr11:9952039-9952040	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs553783935	chr11:9952041-9952042	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs61876942	chr11:9952052-9952053	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs193295641	chr11:9952074-9952075	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs563086246	chr11:9952084-9952085	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs577393102	chr11:9952118-9952119	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs183732452	chr11:9952121-9952122	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs188405376	chr11:9952127-9952128	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs548246604	chr11:9952148-9952149	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs528009546	chr11:9952173-9952174	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs10840328	chr11:9952193-9952194	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs370293700	chr11:9952222-9952223	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs180919268	chr11:9952223-9952224	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs183996269	chr11:9952228-9952229	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs569734741	chr11:9952241-9952242	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs538416865	chr11:9952258-9952259	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs142958353	chr11:9952262-9952263	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs565623260	chr11:9952278-9952279	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs534628465	chr11:9952284-9952285	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs553744993	chr11:9952294-9952295	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs61876943	chr11:9952338-9952339	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs61876944	chr11:9952357-9952358	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556337895	chr11:9952376-9952377	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs576505495	chr11:9952417-9952418	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs539332864	chr11:9952441-9952442	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs545586988	chr11:9952503-9952504	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs368348653	chr11:9952507-9952508	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs565538775	chr11:9952521-9952522	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs61876945	chr11:9952526-9952527	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs117857609	chr11:9952537-9952538	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs151095414	chr11:9952547-9952548	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs560930871	chr11:9952561-9952562	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs529620114	chr11:9952567-9952568	ZNF genes & repeats Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs549768792	chr11:9952625-9952626	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs563201796	chr11:9952626-9952627	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs188680834	chr11:9952637-9952638	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs565226284	chr11:9952645-9952646	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs551931101	chr11:9952646-9952647	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs565582440	chr11:9952662-9952663	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs572379995	chr11:9952675-9952676	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs372023118	chr11:9952726-9952727	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs541111450	chr11:9952739-9952740	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs369524349	chr11:9952742-9952743	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs370011062	chr11:9952816-9952817	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs534593666	chr11:9952845-9952846	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs375250291	chr11:9952865-9952866	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs568345375	chr11:9952877-9952878	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1741 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9878800-9952200	Weak transcription	Aorta	Aorta
2	chr11:9894400-9978600	Weak transcription	Left Ventricle	heart
3	chr11:9910000-9954600	Weak transcription	Pancreas	Pancrea
4	chr11:9917600-9952400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr11:9917800-9952600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr11:9923400-9952200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:9925400-9952200	Weak transcription	Lung	lung
8	chr11:9929000-9952000	Weak transcription	Fetal Lung	lung
9	chr11:9929200-9966800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:9929600-9953000	Weak transcription	HSMMtube	muscle
11	chr11:9934800-9952200	Weak transcription	Fetal Stomach	stomach
12	chr11:9935800-9952000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:9936200-9952000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr11:9941600-9952400	Weak transcription	Fetal Brain Female	brain
15	chr11:9942200-9952200	Weak transcription	Fetal Intestine Large	intestine
16	chr11:9943400-9980600	Weak transcription	Primary T cells from cord blood	blood
17	chr11:9943600-9952200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr11:9944600-9952800	Weak transcription	Liver	Liver
19	chr11:9944800-9952000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:9944800-9952000	Weak transcription	Fetal Muscle Leg	muscle
21	chr11:9944800-9952200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr11:9944800-9952400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr11:9944800-9952400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:9944800-9961000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:9944800-9969000	Weak transcription	Ovary	ovary
26	chr11:9945000-9954000	Weak transcription	HMEC	breast
27	chr11:9945000-9967600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr11:9945400-9952000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr11:9945400-9952200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr11:9945400-9964800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr11:9945600-9955200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr11:9945600-9958400	Weak transcription	NHDF-Ad	bronchial
33	chr11:9945800-9952000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr11:9946400-9952000	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr11:9946400-9952200	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr11:9946600-9952200	Weak transcription	Fetal Intestine Small	intestine
37	chr11:9949000-9952200	Weak transcription	Esophagus	oesophagus
38	chr11:9950200-9980400	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr11:9950600-9952400	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr11:9950600-9952400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr11:9951000-9953000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr11:9951200-9952800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:9951200-9952800	Strong transcription	Adipose Nuclei	Adipose
44	chr11:9951200-9955000	Weak transcription	Right Ventricle	heart
45	chr11:9951400-9952400	Weak transcription	Primary hematopoietic stem cells	blood
46	chr11:9951400-9952400	Strong transcription	Placenta	Placenta
47	chr11:9951600-9953000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr11:9951600-9954400	Weak transcription	Brain Angular Gyrus	brain
49	chr11:9951800-9952400	Enhancers	HepG2	liver
50	chr11:9951800-9952600	Strong transcription	Cortex derived primary cultured neurospheres	brain

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