Variant report

Variant	nsv554197
Chromosome Location	chr11:45673014-45679212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45676873-45677048	K562	blood:	n/a	n/a
2	ATF3	chr11:45676830-45677081	K562	blood:	n/a	n/a
3	ATF3	chr11:45676850-45677177	K562	blood:	n/a	n/a
4	BACH1	chr11:45676782-45677123	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr11:45674503-45674754	K562	blood:	n/a	n/a
6	BHLHE40	chr11:45676651-45677055	K562	blood:	n/a	n/a
7	BHLHE40	chr11:45676951-45677124	GM12878	blood:	n/a	n/a
8	BRCA1	chr11:45676882-45677132	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr11:45676938-45677048	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:45676937-45677275	K562	blood:	n/a	n/a
11	CEBPB	chr11:45676862-45677340	MCF-7	breast:	n/a	n/a
12	CEBPB	chr11:45676840-45677234	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:45676942-45677240	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:45676892-45677278	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr11:45676906-45677182	A549	lung:	n/a	n/a
16	CHD1	chr11:45674129-45674205	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr11:45677074-45677201	HepG2	liver:	n/a	n/a
18	CHD2	chr11:45676856-45677115	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr11:45676842-45677029	K562	blood:	n/a	n/a
20	CHD2	chr11:45676839-45677097	Hela-S3	cervix:	n/a	n/a
21	CREB1	chr11:45676782-45677174	A549	lung:	n/a	n/a
22	CREB1	chr11:45676801-45677320	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr11:45676697-45677340	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr11:45676833-45677132	HUVEC	blood vessel:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
25	CTCF	chr11:45676787-45677075	ECC-1	luminal epithelium:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
26	CTCF	chr11:45676777-45677278	GM12878	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
27	CTCF	chr11:45676920-45677070	HepG2	liver:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
28	CTCF	chr11:45677193-45677332	GM10266	blood:	n/a	n/a
29	CTCF	chr11:45677540-45677690	HVMF	connective:	n/a	chr11:45677577-45677590
30	CTCF	chr11:45676920-45677070	HBMEC	blood vessel:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
31	CTCF	chr11:45677226-45677319	NHEK	skin:	n/a	n/a
32	CTCF	chr11:45676860-45677010	GM06990	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
33	CTCF	chr11:45676920-45677070	HEK293	kidney:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
34	CTCF	chr11:45676920-45677070	SK-N-SH_RA	brain:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
35	CTCF	chr11:45676920-45677070	AG04450	lung:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
36	CTCF	chr11:45676920-45677070	HMF	breast:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
37	CTCF	chr11:45676858-45677101	HepG2	liver:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
38	CTCF	chr11:45677223-45677355	GM13977	blood:	n/a	n/a
39	CTCF	chr11:45676920-45677070	GM12801	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
40	CTCF	chr11:45676700-45676850	GM12870	blood:	n/a	n/a
41	CTCF	chr11:45676855-45677178	GM10266	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
42	CTCF	chr11:45676920-45677070	GM12873	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
43	CTCF	chr11:45676817-45677377	GM19238	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
44	CTCF	chr11:45676920-45677070	GM12871	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
45	CTCF	chr11:45676920-45677070	AG10803	skin:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
46	CTCF	chr11:45676920-45677070	Caco-2	colon:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
47	CTCF	chr11:45676900-45677050	HVMF	connective:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
48	CTCF	chr11:45676920-45677070	HPAF	blood vessel:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
49	CTCF	chr11:45676900-45677050	GM12875	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
50	CTCF	chr11:45676861-45677113	GM20000	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45673410-45673460	CMK	blood:	n/a
2	chr11:45674702-45674752	Hela-S3	cervix:	n/a
3	chr11:45674238-45674288	HEEpiC	esophagus:	n/a
4	chr11:45674238-45674288	HRE	kidney:	n/a
5	chr11:45674702-45674752	HEK293	kidney:	embryo
6	chr11:45673410-45673460	GM19239	blood:	n/a
7	chr11:45673410-45673460	HUVEC	blood vessel:	n/a
8	chr11:45674702-45674752	Caco-2	colon:	n/a
9	chr11:45674702-45674752	BJ	skin:	n/a
10	chr11:45674238-45674288	Hela-S3	cervix:	n/a
11	chr11:45673410-45673460	NHDF-neo	bronchial:	n/a
12	chr11:45673410-45673460	AG04449	skin:	fetal
13	chr11:45673410-45673460	SK-N-MC	brain:	n/a
14	chr11:45673410-45673460	BJ	skin:	n/a
15	chr11:45674238-45674288	HUVEC	blood vessel:	n/a
16	chr11:45674238-45674288	HCPEpiC	choroid plexus:	n/a
17	chr11:45673410-45673460	NH-A	brain:	n/a
18	chr11:45674238-45674288	K562	blood:	n/a
19	chr11:45674702-45674752	HMEC	breast:	n/a
20	chr11:45674238-45674288	GM12891	blood:	n/a
21	chr11:45674238-45674288	NB4	blood:	n/a
22	chr11:45673410-45673460	HIPEpiC	eye:	n/a
23	chr11:45674702-45674752	HRCEpiC	kidney:	n/a
24	chr11:45674702-45674752	SK-N-SH_RA	brain:	n/a
25	chr11:45674238-45674288	NHDF-neo	bronchial:	n/a
26	chr11:45674238-45674288	SK-N-SH_RA	brain:	n/a
27	chr11:45674702-45674752	ovcar-3	ovarian:	n/a
28	chr11:45673410-45673460	HMEC	breast:	n/a
29	chr11:45674702-45674752	HCM	heart:	n/a
30	chr11:45673410-45673460	GM12891	blood:	n/a
31	chr11:45673410-45673460	LNCaP	prostate:	n/a
32	chr11:45673410-45673460	HCT-116	colon:	n/a
33	chr11:45673410-45673460	GM12878	blood:	n/a
34	chr11:45674702-45674752	ProgFib	skin:	n/a
35	chr11:45674702-45674752	GM19239	blood:	n/a
36	chr11:45673410-45673460	AG09319	gingival:	n/a
37	chr11:45674238-45674288	AG04450	lung:	fetal
38	chr11:45673410-45673460	PANC-1	pancreas:	n/a
39	chr11:45674238-45674288	AG09319	gingival:	n/a
40	chr11:45673410-45673460	SKMC	muscle:	n/a
41	chr11:45673410-45673460	AG10803	skin:	n/a
42	chr11:45674238-45674288	HNPCEpiC	eye:	n/a
43	chr11:45674238-45674288	PFSK-1	brain:	n/a
44	chr11:45674238-45674288	HPAEpiC	pulmonary alveolar:	n/a
45	chr11:45674702-45674752	SK-N-SH	brain:	n/a
46	chr11:45674238-45674288	SAEC	small airway:	n/a
47	chr11:45673410-45673460	Hela-S3	cervix:	n/a
48	chr11:45674702-45674752	LNCaP	prostate:	n/a
49	chr11:45673410-45673460	HRE	kidney:	n/a
50	chr11:45674702-45674752	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:45677224..45679884-chr11:45774991..45777658,2	MCF-7	breast:
2	chr11:45673703..45676177-chr11:45681263..45683293,2	K562	blood:
3	chr11:45658659..45661256-chr11:45675243..45676992,2	K562	blood:
4	chr11:45671225..45673031-chr11:45675062..45677985,2	K562	blood:
5	chr11:45671225..45673031-chr11:45675062..45677985,2	K562	blood:
6	chr11:45676348..45677919-chr11:45792905..45794177,5	K562	blood:
7	chr11:45678783..45681662-chr11:45685006..45688205,4	MCF-7	breast:
8	chr11:45673604..45675879-chr11:45677397..45678906,2	K562	blood:
9	chr11:45392488..45393362-chr11:45676466..45677098,3	MCF-7	breast:
10	chr11:45673604..45675879-chr11:45677397..45678906,2	K562	blood:
11	chr11:45427814..45428397-chr11:45676543..45677286,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf94-5	chr11:45674071-45674156	NONHSAT019041
2	lnc-CTD-2210P24.4.1-2	chr11:45674019-45674355	NONHSAT019042
3	lnc-CTD-2210P24.4.1-2	chr11:45672876-45673104	NONHSAT019042
4	lnc-CTD-2210P24.4.1-2	chr11:45673079-45673104	ENSG00000255091.1
5	lnc-CTD-2210P24.4.1-2	chr11:45674019-45674241	ENSG00000255091.1
6	lnc-C11orf94-5	chr11:45672783-45673640	NONHSAT019041

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

Extended variants
information (count: 219 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:219 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4148900	chr11:45673014-45673015	Weak transcription Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536310135	chr11:45673059-45673060	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs552913382	chr11:45673093-45673094	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs573021892	chr11:45673184-45673185	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs544861343	chr11:45673219-45673220	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs558464057	chr11:45673239-45673240	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs575180492	chr11:45673280-45673281	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs559240107	chr11:45673300-45673301	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs561994722	chr11:45673371-45673372	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs144849349	chr11:45673372-45673373	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs369918656	chr11:45673410-45673411	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs530151721	chr11:45673411-45673412	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs540697229	chr11:45673421-45673422	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs560364549	chr11:45673422-45673423	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs45604634	chr11:45673446-45673447	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs45533136	chr11:45673493-45673494	Weak transcription Enhancers Strong transcription Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs569571514	chr11:45673620-45673621	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
18	rs532000717	chr11:45673664-45673665	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs71451614	chr11:45673699-45673700	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs71451615	chr11:45673704-45673705	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs550609174	chr11:45673731-45673732	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs376554519	chr11:45673794-45673795	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs45560037	chr11:45673957-45673958	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs35254532	chr11:45674019-45674020	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
25	rs553067425	chr11:45674020-45674021	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
26	rs138003314	chr11:45674062-45674063	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
27	rs543396238	chr11:45674063-45674064	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
28	rs538874903	chr11:45674065-45674066	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs558285192	chr11:45674085-45674086	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs575183807	chr11:45674099-45674100	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs544069621	chr11:45674100-45674101	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs2277272	chr11:45674170-45674171	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs573376847	chr11:45674201-45674202	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs574807805	chr11:45674212-45674213	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs4148899	chr11:45674266-45674267	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs45457491	chr11:45674348-45674349	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs45480804	chr11:45674387-45674388	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs149483276	chr11:45674393-45674394	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147517520	chr11:45674482-45674483	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs559036091	chr11:45674511-45674512	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs563035736	chr11:45674538-45674539	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs532065239	chr11:45674557-45674558	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs45535741	chr11:45674580-45674581	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs562353744	chr11:45674583-45674584	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs4148898	chr11:45674599-45674600	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs376335980	chr11:45674647-45674648	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs372225694	chr11:45674681-45674682	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs566566112	chr11:45674703-45674704	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs538316802	chr11:45674713-45674714	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs201164593	chr11:45674729-45674730	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	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:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45665600-45674400	Weak transcription	HMEC	breast
2	chr11:45665600-45680000	Weak transcription	Gastric	stomach
3	chr11:45669200-45674000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr11:45669800-45673200	Weak transcription	Brain Angular Gyrus	brain
5	chr11:45669800-45676400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:45669800-45676400	Weak transcription	HUVEC	blood vessel
7	chr11:45669800-45676600	Weak transcription	Left Ventricle	heart
8	chr11:45670000-45680200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:45670200-45673800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:45670600-45673200	Strong transcription	Ovary	ovary
11	chr11:45670600-45673800	Strong transcription	Fetal Brain Female	brain
12	chr11:45670600-45675400	Strong transcription	Dnd41	blood
13	chr11:45670600-45676600	Weak transcription	Brain Hippocampus Middle	brain
14	chr11:45671200-45673200	Strong transcription	Brain Cingulate Gyrus	brain
15	chr11:45671200-45673400	Strong transcription	Brain Anterior Caudate	brain
16	chr11:45671200-45673400	Strong transcription	Lung	lung
17	chr11:45671200-45676200	Weak transcription	Fetal Brain Male	brain
18	chr11:45671800-45673600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:45671800-45674200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:45672000-45673600	Strong transcription	Brain Germinal Matrix	brain
21	chr11:45672000-45673800	Weak transcription	Fetal Muscle Leg	muscle
22	chr11:45672200-45673400	Strong transcription	Brain Inferior Temporal Lobe	brain
23	chr11:45672400-45673400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:45672600-45675200	Weak transcription	Aorta	Aorta
25	chr11:45672600-45675800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:45672600-45676400	Weak transcription	Right Ventricle	heart
27	chr11:45672800-45674200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr11:45673000-45673600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr11:45673000-45673600	Strong transcription	Spleen	Spleen
30	chr11:45673200-45673400	Strong transcription	Brain Angular Gyrus	brain
31	chr11:45673200-45674200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr11:45673200-45675400	Weak transcription	Brain Cingulate Gyrus	brain
33	chr11:45673200-45677000	Weak transcription	Ovary	ovary
34	chr11:45673400-45673600	Weak transcription	Brain Angular Gyrus	brain
35	chr11:45673400-45674200	Bivalent Enhancer	Fetal Stomach	stomach
36	chr11:45673400-45674400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr11:45673400-45674600	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr11:45673400-45675800	Weak transcription	Brain Anterior Caudate	brain
39	chr11:45673400-45677000	Weak transcription	Lung	lung
40	chr11:45673600-45673800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr11:45673600-45673800	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr11:45673600-45673800	Genic enhancers	Spleen	Spleen
43	chr11:45673600-45674000	Genic enhancers	Brain Angular Gyrus	brain
44	chr11:45673600-45674200	Enhancers	Placenta Amnion	Placenta Amnion
45	chr11:45673600-45674600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr11:45673600-45676000	Weak transcription	Brain Germinal Matrix	brain
47	chr11:45673600-45677200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:45673800-45674200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:45673800-45674200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:45673800-45674200	Bivalent/Poised TSS	Hela-S3	cervix

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