Variant report

Variant	nsv554198
Chromosome Location	chr11:45674266-45684117
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	chr11:45676862-45677340	MCF-7	breast:	n/a	n/a
11	CEBPB	chr11:45676892-45677278	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr11:45676937-45677275	K562	blood:	n/a	n/a
13	CEBPB	chr11:45676840-45677234	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:45676906-45677182	A549	lung:	n/a	n/a
15	CEBPB	chr11:45676942-45677240	HepG2	liver:	n/a	n/a
16	CHD2	chr11:45677074-45677201	HepG2	liver:	n/a	n/a
17	CHD2	chr11:45676839-45677097	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr11:45676842-45677029	K562	blood:	n/a	n/a
19	CHD2	chr11:45676856-45677115	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr11:45676782-45677174	A549	lung:	n/a	n/a
21	CREB1	chr11:45676801-45677320	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr11:45676697-45677340	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr11:45676920-45677070	SK-N-SH_RA	brain:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
24	CTCF	chr11:45676940-45677090	HFF	foreskin:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
25	CTCF	chr11:45676860-45677010	GM06990	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
26	CTCF	chr11:45676920-45677070	AG04450	lung:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
27	CTCF	chr11:45676834-45677152	Kidney_OC	kidney:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
28	CTCF	chr11:45676900-45677050	SAEC	small airway:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
29	CTCF	chr11:45676880-45677030	NHEK	skin:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
30	CTCF	chr11:45676845-45677148	Fibrobl	skin:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
31	CTCF	chr11:45676900-45677050	HMEC	breast:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
32	CTCF	chr11:45676843-45677160	HepG2	liver:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
33	CTCF	chr11:45676920-45677070	GM12867	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
34	CTCF	chr11:45676940-45677090	HepG2	liver:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
35	CTCF	chr11:45676900-45677050	HAc	cerebellar:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
36	CTCF	chr11:45676900-45677050	HA-sp	spinal cord:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
37	CTCF	chr11:45676737-45677169	MCF-7	breast:	n/a	chr11:45676980-45676988 chr11:45676970-45676991 chr11:45676975-45676993
38	CTCF	chr11:45676860-45677131	Pancreas_OC	pancreas:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
39	CTCF	chr11:45676845-45677183	H1-hESC	embryonic stem cell:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
40	CTCF	chr11:45676920-45677070	GM12871	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
41	CTCF	chr11:45676805-45677192	K562	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
42	CTCF	chr11:45676854-45677142	Hela-S3	cervix:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
43	CTCF	chr11:45676880-45677030	GM12864	blood:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
44	CTCF	chr11:45676920-45677070	NHDF-neo	bronchial:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
45	CTCF	chr11:45676900-45677050	WI-38	lung:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
46	CTCF	chr11:45676240-45676390	GM12874	blood:	n/a	n/a
47	CTCF	chr11:45676837-45677152	Spleen_OC	spleen:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
48	CTCF	chr11:45676612-45677267	HCT-116	colon:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991
49	CTCF	chr11:45677223-45677355	GM13977	blood:	n/a	n/a
50	CTCF	chr11:45676880-45677030	HCM	heart:	n/a	chr11:45676975-45676993 chr11:45676980-45676988 chr11:45676970-45676991

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45674238-45674288	LNCaP	prostate:	n/a
2	chr11:45683401-45683451	HIPEpiC	eye:	n/a
3	chr11:45683401-45683451	T-47D	breast:	n/a
4	chr11:45674238-45674288	HRPEpiC	eye:	n/a
5	chr11:45674702-45674752	AG10803	skin:	n/a
6	chr11:45674702-45674752	HCF	heart:	n/a
7	chr11:45683401-45683451	GM12892	blood:	n/a
8	chr11:45674702-45674752	GM19239	blood:	n/a
9	chr11:45674702-45674752	NH-A	brain:	n/a
10	chr11:45674702-45674752	HIPEpiC	eye:	n/a
11	chr11:45683401-45683451	AG09309	skin:	n/a
12	chr11:45674702-45674752	SKMC	muscle:	n/a
13	chr11:45674238-45674288	BJ	skin:	n/a
14	chr11:45674238-45674288	HNPCEpiC	eye:	n/a
15	chr11:45674238-45674288	Jurkat	blood:	n/a
16	chr11:45683401-45683451	NH-A	brain:	n/a
17	chr11:45674238-45674288	HEK293	kidney:	embryo
18	chr11:45683401-45683451	Hepatocyte	liver:	n/a
19	chr11:45674238-45674288	PrEC	prostate:	n/a
20	chr11:45674702-45674752	NT2-D1	testis:	n/a
21	chr11:45674238-45674288	U87	brain:	n/a
22	chr11:45674238-45674288	PFSK-1	brain:	n/a
23	chr11:45674702-45674752	HRCEpiC	kidney:	n/a
24	chr11:45674702-45674752	HEK293	kidney:	embryo
25	chr11:45674702-45674752	ECC-1	luminal epithelium:	n/a
26	chr11:45674702-45674752	PrEC	prostate:	n/a
27	chr11:45674702-45674752	GM12892	blood:	n/a
28	chr11:45674238-45674288	H1-hESC	embryonic stem cell:	embryo
29	chr11:45674702-45674752	HCPEpiC	choroid plexus:	n/a
30	chr11:45674702-45674752	SK-N-MC	brain:	n/a
31	chr11:45683401-45683451	NT2-D1	testis:	n/a
32	chr11:45674238-45674288	ovcar-3	ovarian:	n/a
33	chr11:45674702-45674752	RPTEC	kidney:	n/a
34	chr11:45674238-45674288	T-47D	breast:	n/a
35	chr11:45674702-45674752	AG04449	skin:	fetal
36	chr11:45674238-45674288	SKMC	muscle:	n/a
37	chr11:45674702-45674752	AG09319	gingival:	n/a
38	chr11:45674702-45674752	Hela-S3	cervix:	n/a
39	chr11:45674238-45674288	MCF10A-Er-Src	breast:	n/a
40	chr11:45674702-45674752	HCM	heart:	n/a
41	chr11:45674702-45674752	SAEC	small airway:	n/a
42	chr11:45674238-45674288	SK-N-MC	brain:	n/a
43	chr11:45683401-45683451	Caco-2	colon:	n/a
44	chr11:45674702-45674752	K562	blood:	n/a
45	chr11:45683401-45683451	GM12891	blood:	n/a
46	chr11:45683401-45683451	HUVEC	blood vessel:	n/a
47	chr11:45683401-45683451	HL-60	blood:	n/a
48	chr11:45674238-45674288	CMK	blood:	n/a
49	chr11:45674238-45674288	HRCEpiC	kidney:	n/a
50	chr11:45683401-45683451	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:45677224..45679884-chr11:45774991..45777658,2	MCF-7	breast:
2	chr11:45673604..45675879-chr11:45677397..45678906,2	K562	blood:
3	chr11:45673604..45675879-chr11:45677397..45678906,2	K562	blood:
4	chr11:45671225..45673031-chr11:45675062..45677985,2	K562	blood:
5	chr11:45392488..45393362-chr11:45676466..45677098,3	MCF-7	breast:
6	chr11:45678783..45681662-chr11:45685006..45688205,4	MCF-7	breast:
7	chr11:45676348..45677919-chr11:45792905..45794177,5	K562	blood:
8	chr11:45427814..45428397-chr11:45676543..45677286,2	MCF-7	breast:
9	chr11:45672171..45675080-chr11:45682496..45685022,2	K562	blood:
10	chr11:45673703..45676177-chr11:45681263..45683293,2	K562	blood:
11	chr11:45673703..45676177-chr11:45681263..45683293,2	K562	blood:
12	chr11:45658659..45661256-chr11:45675243..45676992,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2210P24.4.1-2	chr11:45674019-45674355	NONHSAT019042

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

Extended variants
information (count: 374 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	rs45457491	chr11:45674348-45674349	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	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
4	rs149483276	chr11:45674393-45674394	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147517520	chr11:45674482-45674483	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559036091	chr11:45674511-45674512	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs563035736	chr11:45674538-45674539	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs532065239	chr11:45674557-45674558	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	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
10	rs562353744	chr11:45674583-45674584	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	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
12	rs376335980	chr11:45674647-45674648	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs372225694	chr11:45674681-45674682	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs566566112	chr11:45674703-45674704	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs538316802	chr11:45674713-45674714	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs201164593	chr11:45674729-45674730	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs551970101	chr11:45674798-45674799	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568686000	chr11:45674803-45674804	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545284378	chr11:45674825-45674826	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs45593638	chr11:45674841-45674842	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574639181	chr11:45674868-45674869	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565565680	chr11:45674870-45674871	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181762461	chr11:45674877-45674878	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375289422	chr11:45674882-45674883	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs80277561	chr11:45674930-45674931	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529162350	chr11:45674937-45674938	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546290642	chr11:45674944-45674945	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531158805	chr11:45674983-45674984	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562949039	chr11:45675071-45675072	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10679625	chr11:45675081-45675082	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10668083	chr11:45675082-45675083	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78808504	chr11:45675088-45675089	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542433892	chr11:45675098-45675099	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138040842	chr11:45675174-45675175	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184367290	chr11:45675175-45675176	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527933988	chr11:45675205-45675206	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546585985	chr11:45675240-45675241	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78452006	chr11:45675243-45675244	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532258083	chr11:45675311-45675312	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551883999	chr11:45675359-45675360	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113782002	chr11:45675402-45675403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76211024	chr11:45675420-45675421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537692663	chr11:45675489-45675490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530134670	chr11:45675510-45675511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547932504	chr11:45675556-45675557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116703919	chr11:45675607-45675608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573644972	chr11:45675614-45675615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533810316	chr11:45675629-45675630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534500181	chr11:45675635-45675636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554157856	chr11:45675661-45675662	Weak transcription Enhancers	n/a	n/a	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:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr11:45669800-45676400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:45669800-45676400	Weak transcription	HUVEC	blood vessel
5	chr11:45669800-45676600	Weak transcription	Left Ventricle	heart
6	chr11:45670000-45680200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:45670600-45675400	Strong transcription	Dnd41	blood
8	chr11:45670600-45676600	Weak transcription	Brain Hippocampus Middle	brain
9	chr11:45671200-45676200	Weak transcription	Fetal Brain Male	brain
10	chr11:45672600-45675200	Weak transcription	Aorta	Aorta
11	chr11:45672600-45675800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr11:45672600-45676400	Weak transcription	Right Ventricle	heart
13	chr11:45673200-45675400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr11:45673200-45677000	Weak transcription	Ovary	ovary
15	chr11:45673400-45674400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:45673400-45674600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr11:45673400-45675800	Weak transcription	Brain Anterior Caudate	brain
18	chr11:45673400-45677000	Weak transcription	Lung	lung
19	chr11:45673600-45674600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr11:45673600-45676000	Weak transcription	Brain Germinal Matrix	brain
21	chr11:45673600-45677200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:45673800-45674400	Strong transcription	Spleen	Spleen
23	chr11:45673800-45674600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr11:45673800-45674600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr11:45673800-45675000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr11:45673800-45676600	Weak transcription	Fetal Brain Female	brain
27	chr11:45673800-45677400	Enhancers	Fetal Muscle Leg	muscle
28	chr11:45674000-45674600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr11:45674000-45674800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr11:45674000-45674800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:45674000-45674800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr11:45674000-45674800	Enhancers	Brain Angular Gyrus	brain
33	chr11:45674000-45675000	Enhancers	NHEK	skin
34	chr11:45674000-45675000	Enhancers	Osteobl	bone
35	chr11:45674000-45675600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:45674000-45677200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr11:45674200-45674400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:45674200-45674600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr11:45674200-45674600	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr11:45674200-45674800	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr11:45674200-45674800	Enhancers	NHDF-Ad	bronchial
42	chr11:45674200-45676000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:45674200-45677000	Enhancers	Fetal Stomach	stomach
44	chr11:45674200-45679800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr11:45674400-45674600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr11:45674400-45674600	Enhancers	HMEC	breast
47	chr11:45674400-45676400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:45674400-45676400	Weak transcription	Spleen	Spleen
49	chr11:45674400-45677000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:45674600-45674800	Enhancers	Skeletal Muscle Female	skeletal muscle

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