Variant report

Variant	nsv897400
Chromosome Location	chr11:48878863-48960697
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1734)
CpG islands
(count:794)
Chromatin interactive
region (count:1)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1734 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48880376-48880748	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48895975-48896341	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48892892-48893269	HepG2	liver:	n/a	n/a
4	ATF1	chr11:48892890-48893270	K562	blood:	n/a	n/a
5	ATF1	chr11:48880374-48880748	K562	blood:	n/a	n/a
6	ATF1	chr11:48940082-48940286	K562	blood:	n/a	n/a
7	ATF1	chr11:48896850-48897050	K562	blood:	n/a	n/a
8	ATF1	chr11:48895825-48896343	K562	blood:	n/a	n/a
9	ATF1	chr11:48883351-48883720	K562	blood:	n/a	n/a
10	ATF3	chr11:48892858-48893151	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:48881669-48882080	K562	blood:	n/a	n/a
12	BACH1	chr11:48956270-48956471	K562	blood:	n/a	n/a
13	BATF	chr11:48931968-48932274	GM12878	blood:	n/a	n/a
14	BATF	chr11:48934117-48934343	GM12878	blood:	n/a	n/a
15	BATF	chr11:48894608-48895288	GM12878	blood:	n/a	n/a
16	BATF	chr11:48953227-48953611	GM12878	blood:	n/a	n/a
17	BATF	chr11:48883213-48883919	GM12878	blood:	n/a	n/a
18	BATF	chr11:48935181-48935425	GM12878	blood:	n/a	n/a
19	BATF	chr11:48895948-48896327	GM12878	blood:	n/a	n/a
20	BATF	chr11:48898958-48899437	GM12878	blood:	n/a	n/a
21	BATF	chr11:48946385-48946719	GM12878	blood:	n/a	n/a
22	BATF	chr11:48945095-48945310	GM12878	blood:	n/a	n/a
23	BATF	chr11:48886811-48887099	GM12878	blood:	n/a	n/a
24	BATF	chr11:48883215-48883597	GM12878	blood:	n/a	n/a
25	BATF	chr11:48934428-48934662	GM12878	blood:	n/a	n/a
26	BATF	chr11:48887996-48888565	GM12878	blood:	n/a	n/a
27	BATF	chr11:48892880-48893156	GM12878	blood:	n/a	n/a
28	BATF	chr11:48943793-48944288	GM12878	blood:	n/a	n/a
29	BATF	chr11:48934181-48934321	GM12878	blood:	n/a	n/a
30	BATF	chr11:48888085-48888631	GM12878	blood:	n/a	n/a
31	BATF	chr11:48916618-48916954	GM12878	blood:	n/a	chr11:48916904-48916914
32	BATF	chr11:48885554-48885939	GM12878	blood:	n/a	n/a
33	BATF	chr11:48906543-48906879	GM12878	blood:	n/a	chr11:48906618-48906628
34	BATF	chr11:48894524-48895290	GM12878	blood:	n/a	n/a
35	BATF	chr11:48895950-48896265	GM12878	blood:	n/a	n/a
36	BATF	chr11:48945011-48945390	GM12878	blood:	n/a	n/a
37	BATF	chr11:48916722-48917006	GM12878	blood:	n/a	chr11:48916904-48916914
38	BATF	chr11:48955305-48955628	GM12878	blood:	n/a	n/a
39	BATF	chr11:48934446-48934684	GM12878	blood:	n/a	n/a
40	BATF	chr11:48940420-48940720	GM12878	blood:	n/a	n/a
41	BATF	chr11:48885664-48885889	GM12878	blood:	n/a	n/a
42	BATF	chr11:48953209-48953631	GM12878	blood:	n/a	n/a
43	BATF	chr11:48932107-48932317	GM12878	blood:	n/a	n/a
44	BATF	chr11:48898982-48899252	GM12878	blood:	n/a	n/a
45	BATF	chr11:48946780-48947152	GM12878	blood:	n/a	n/a
46	BATF	chr11:48906491-48906775	GM12878	blood:	n/a	chr11:48906618-48906628
47	BCL11A	chr11:48898876-48899221	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:48878722-48879245	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:48900350-48900563	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:48882429-48882725	GM12878	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48901705-48901755	T-47D	breast:	n/a
2	chr11:48901705-48901755	T-47D	breast:	n/a
3	chr11:48923668-48923718	BJ	skin:	n/a
4	chr11:48922741-48922791	T-47D	breast:	n/a
5	chr11:48922271-48922321	HUVEC	blood vessel:	n/a
6	chr11:48880009-48880059	LNCaP	prostate:	n/a
7	chr11:48880009-48880059	AG09309	skin:	n/a
8	chr11:48922674-48922724	AG09309	skin:	n/a
9	chr11:48880009-48880059	ECC-1	luminal epithelium:	n/a
10	chr11:48922271-48922321	HIPEpiC	eye:	n/a
11	chr11:48901914-48901964	SAEC	small airway:	n/a
12	chr11:48924804-48924854	HCT-116	colon:	n/a
13	chr11:48922741-48922791	IMR90	lung:	fetal
14	chr11:48922741-48922791	NT2-D1	testis:	n/a
15	chr11:48924804-48924854	BJ	skin:	n/a
16	chr11:48901705-48901755	HIPEpiC	eye:	n/a
17	chr11:48923392-48923442	HEK293	kidney:	embryo
18	chr11:48923577-48923627	SK-N-SH_RA	brain:	n/a
19	chr11:48902014-48902064	NHBE	bronchial:	n/a
20	chr11:48922271-48922321	H1-hESC	embryonic stem cell:	embryo
21	chr11:48922269-48922319	GM12892	blood:	n/a
22	chr11:48922269-48922319	CMK	blood:	n/a
23	chr11:48923577-48923627	PrEC	prostate:	n/a
24	chr11:48902014-48902064	Hela-S3	cervix:	n/a
25	chr11:48923668-48923718	SK-N-SH_RA	brain:	n/a
26	chr11:48922741-48922791	MCF-7	breast:	n/a
27	chr11:48924804-48924854	MCF10A-Er-Src	breast:	n/a
28	chr11:48901705-48901755	HEEpiC	esophagus:	n/a
29	chr11:48922035-48922085	SKMC	muscle:	n/a
30	chr11:48923392-48923442	Hepatocyte	liver:	n/a
31	chr11:48901914-48901964	Caco-2	colon:	n/a
32	chr11:48923392-48923442	NHBE	bronchial:	n/a
33	chr11:48880009-48880059	HNPCEpiC	eye:	n/a
34	chr11:48902014-48902064	GM19239	blood:	n/a
35	chr11:48923392-48923442	SAEC	small airway:	n/a
36	chr11:48924804-48924854	HepG2	liver:	n/a
37	chr11:48924804-48924854	HIPEpiC	eye:	n/a
38	chr11:48922035-48922085	NH-A	brain:	n/a
39	chr11:48922271-48922321	Hela-S3	cervix:	n/a
40	chr11:48922271-48922321	HEEpiC	esophagus:	n/a
41	chr11:48923392-48923442	MCF10A-Er-Src	breast:	n/a
42	chr11:48901914-48901964	HCF	heart:	n/a
43	chr11:48922269-48922319	MCF-7	breast:	n/a
44	chr11:48922271-48922321	MCF10A-Er-Src	breast:	n/a
45	chr11:48880009-48880059	HCF	heart:	n/a
46	chr11:48880009-48880059	A549	lung:	n/a
47	chr11:48902014-48902064	ProgFib	skin:	n/a
48	chr11:48923668-48923718	K562	blood:	n/a
49	chr11:48901914-48901964	GM12878	blood:	n/a
50	chr11:48922035-48922085	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:121484902..121485419-chr11:48946286..48946806,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC084851.1-5	chr11:48919940-48920255	NONHSAT021301
2	lnc-AC084851.1-5	chr11:48919540-48919822	NONHSAT021301
3	lnc-AC084851.1-5	chr11:48914808-48914900	NONHSAT021301
4	lnc-AC084851.1-4	chr11:48929840-48930498	NONHSAT021302
5	lnc-AC084851.1-4	chr11:48928655-48928750	NONHSAT021302
6	lnc-AC084851.1-5	chr11:48916513-48916636	NONHSAT021301

No data

Variant related genes	Relation type
ENSG00000255527	TF binding region
ENSG00000255551	TF binding region
ENSG00000254920	TF binding region
ENSG00000254728	TF binding region
ENSG00000255527	CpG island
ENSG00000255551	CpG island
ENSG00000254920	CpG island
ENSG00000254728	CpG island

Extended variants
information (count: 6575 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:6575 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10839138	chr11:48878863-48878864	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143474649	chr11:48878865-48878866	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150799886	chr11:48878868-48878869	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537737150	chr11:48878877-48878878	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556943886	chr11:48878880-48878881	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573649131	chr11:48878887-48878888	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538402056	chr11:48878888-48878889	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553158306	chr11:48878897-48878898	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs202162157	chr11:48878900-48878901	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372319685	chr11:48878901-48878902	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573271117	chr11:48878911-48878912	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373085129	chr11:48878924-48878925	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376493521	chr11:48878925-48878926	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375644529	chr11:48878929-48878930	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10839139	chr11:48878930-48878931	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201334384	chr11:48878932-48878933	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565474608	chr11:48878935-48878936	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10839140	chr11:48878937-48878938	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111307816	chr11:48878944-48878945	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112449371	chr11:48878949-48878950	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs61897767	chr11:48878956-48878957	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200323225	chr11:48878960-48878961	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544881056	chr11:48878965-48878966	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369767909	chr11:48878974-48878975	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199777876	chr11:48878982-48878983	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201556354	chr11:48879003-48879004	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560871081	chr11:48879014-48879015	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199567631	chr11:48879016-48879017	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371782855	chr11:48879027-48879028	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111895707	chr11:48879031-48879032	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111834732	chr11:48879032-48879033	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188869231	chr11:48879038-48879039	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537503395	chr11:48879059-48879060	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200617953	chr11:48879060-48879061	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557495934	chr11:48879083-48879084	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181251616	chr11:48879111-48879112	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546694193	chr11:48879118-48879119	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373575395	chr11:48879119-48879120	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532215026	chr11:48879120-48879121	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536688459	chr11:48879130-48879131	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79513213	chr11:48879133-48879134	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555617858	chr11:48879141-48879142	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568669186	chr11:48879157-48879158	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374721315	chr11:48879159-48879160	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537749326	chr11:48879164-48879165	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368826784	chr11:48879167-48879168	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185458635	chr11:48879174-48879175	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572275147	chr11:48879184-48879185	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200951376	chr11:48879185-48879186	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201630931	chr11:48879192-48879193	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48868000-48880400	Weak transcription	Psoas Muscle	Psoas
2	chr11:48868000-48893000	Weak transcription	K562	blood
3	chr11:48876800-48883800	ZNF genes & repeats	Primary T cells from cord blood	blood
4	chr11:48876800-48884000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:48876800-48885400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr11:48878600-48879000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
7	chr11:48879200-48880400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr11:48879600-48886000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr11:48880000-48881200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
10	chr11:48880200-48882600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
11	chr11:48880400-48880600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:48880400-48880600	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
13	chr11:48880400-48880600	ZNF genes & repeats	Stomach Mucosa	stomach
14	chr11:48880400-48880600	Enhancers	HSMMtube	muscle
15	chr11:48880400-48880800	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:48880400-48880800	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:48880400-48880800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:48880400-48880800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
19	chr11:48880400-48880800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
20	chr11:48880400-48880800	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:48880400-48880800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
22	chr11:48880400-48880800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
23	chr11:48880400-48880800	ZNF genes & repeats	Adipose Nuclei	Adipose
24	chr11:48880400-48880800	Active TSS	Aorta	Aorta
25	chr11:48880400-48880800	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
26	chr11:48880400-48880800	ZNF genes & repeats	Brain Substantia Nigra	brain
27	chr11:48880400-48880800	ZNF genes & repeats	Gastric	stomach
28	chr11:48880400-48880800	Active TSS	Psoas Muscle	Psoas
29	chr11:48880400-48880800	ZNF genes & repeats	HUVEC	blood vessel
30	chr11:48880400-48881000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr11:48880400-48882000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
32	chr11:48880400-48883800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr11:48880400-48885400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
34	chr11:48880600-48880800	Bivalent/Poised TSS	Primary T helper naive cells fromperipheralblood	blood
35	chr11:48880600-48880800	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr11:48880600-48880800	ZNF genes & repeats	Colon Smooth Muscle	Colon
37	chr11:48880600-48883200	Weak transcription	HSMMtube	muscle
38	chr11:48880600-48883400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr11:48880800-48881800	Weak transcription	Brain Substantia Nigra	brain
40	chr11:48880800-48881800	Weak transcription	HUVEC	blood vessel
41	chr11:48880800-48883200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr11:48880800-48883400	Weak transcription	Aorta	Aorta
43	chr11:48880800-48883400	Weak transcription	Colon Smooth Muscle	Colon
44	chr11:48881400-48883000	ZNF genes & repeats	HepG2	liver
45	chr11:48881400-48887000	Weak transcription	NHDF-Ad	bronchial
46	chr11:48881800-48882000	ZNF genes & repeats	HUVEC	blood vessel
47	chr11:48881800-48882200	ZNF genes & repeats	Brain Substantia Nigra	brain
48	chr11:48882000-48882800	Weak transcription	HUVEC	blood vessel
49	chr11:48882400-48883600	ZNF genes & repeats	Brain Substantia Nigra	brain
50	chr11:48882400-48883800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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