Variant report

Variant	nsv551844
Chromosome Location	chr10:90879304-90899444
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	BATF	chr10:90883079-90883398	GM12878	blood:	n/a	chr10:90883278-90883289
2	CEBPB	chr10:90898642-90898953	HepG2	liver:	n/a	chr10:90898785-90898798 chr10:90898786-90898797
3	CEBPB	chr10:90898646-90898929	A549	lung:	n/a	chr10:90898785-90898798 chr10:90898786-90898797
4	CEBPB	chr10:90898625-90898979	IMR90	lung:	n/a	chr10:90898785-90898798 chr10:90898786-90898797
5	CEBPB	chr10:90889682-90890041	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr10:90881526-90881717	HepG2	liver:	n/a	n/a
7	CEBPB	chr10:90889718-90890002	IMR90	lung:	n/a	n/a
8	CEBPB	chr10:90898602-90898986	Hela-S3	cervix:	n/a	chr10:90898785-90898798 chr10:90898786-90898797
9	CTCF	chr10:90888880-90889030	AG04450	lung:	n/a	n/a
10	CTCF	chr10:90882324-90882355	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr10:90889780-90889809	Fibrobl	skin:	n/a	n/a
12	E2F4	chr10:90882014-90882562	MCF10A-Er-Src	breast:	n/a	n/a
13	EP300	chr10:90889659-90889977	SK-N-SH_RA	brain:	n/a	n/a
14	EP300	chr10:90894744-90895039	GM12878	blood:	n/a	n/a
15	EP300	chr10:90889655-90890037	SK-N-SH_RA	brain:	n/a	chr10:90889965-90889979
16	EP300	chr10:90889762-90889989	Hela-S3	cervix:	n/a	chr10:90889965-90889979
17	EP300	chr10:90898612-90898919	Hela-S3	cervix:	n/a	chr10:90898783-90898797
18	EP300	chr10:90889386-90890214	SK-N-SH	brain:	n/a	chr10:90889965-90889979
19	EP300	chr10:90894714-90895050	GM12878	blood:	n/a	n/a
20	FOS	chr10:90880830-90880952	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr10:90889718-90890012	MCF10A-Er-Src	breast:	n/a	chr10:90889798-90889806
22	FOS	chr10:90889685-90890011	MCF10A-Er-Src	breast:	n/a	chr10:90889798-90889806
23	FOS	chr10:90889727-90890064	MCF10A-Er-Src	breast:	n/a	chr10:90889798-90889806
24	FOS	chr10:90882235-90882568	MCF10A-Er-Src	breast:	n/a	chr10:90882401-90882409 chr10:90882401-90882410 chr10:90882399-90882411 chr10:90882402-90882409 chr10:90882400-90882410 chr10:90882397-90882408 chr10:90882399-90882410
25	FOS	chr10:90882243-90882564	MCF10A-Er-Src	breast:	n/a	chr10:90882401-90882409 chr10:90882401-90882410 chr10:90882399-90882411 chr10:90882402-90882409 chr10:90882400-90882410 chr10:90882397-90882408 chr10:90882399-90882410
26	FOS	chr10:90882204-90882661	MCF10A-Er-Src	breast:	n/a	chr10:90882401-90882409 chr10:90882401-90882410 chr10:90882399-90882411 chr10:90882402-90882409 chr10:90882400-90882410 chr10:90882397-90882408 chr10:90882399-90882410
27	FOS	chr10:90882142-90882771	HUVEC	blood vessel:	n/a	chr10:90882401-90882409 chr10:90882401-90882410 chr10:90882399-90882411 chr10:90882402-90882409 chr10:90882400-90882410 chr10:90882397-90882408 chr10:90882399-90882410
28	FOS	chr10:90889668-90890046	MCF10A-Er-Src	breast:	n/a	chr10:90889798-90889806
29	FOS	chr10:90882236-90882587	MCF10A-Er-Src	breast:	n/a	chr10:90882401-90882409 chr10:90882401-90882410 chr10:90882399-90882411 chr10:90882402-90882409 chr10:90882400-90882410 chr10:90882397-90882408 chr10:90882399-90882410
30	GATA2	chr10:90890432-90890858	SH-SY5Y	brain:	n/a	n/a
31	GATA2	chr10:90889625-90890169	SH-SY5Y	brain:	n/a	chr10:90889967-90889978
32	GATA3	chr10:90889616-90890082	SK-N-SH	brain:	n/a	chr10:90889967-90889978
33	GATA3	chr10:90889711-90890551	SH-SY5Y	brain:	n/a	chr10:90889967-90889978
34	GATA3	chr10:90898407-90898596	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr10:90889598-90890115	SK-N-SH	brain:	n/a	chr10:90889967-90889978
36	GATA3	chr10:90889680-90890008	T-47D	breast:	n/a	chr10:90889967-90889978
37	JUN	chr10:90882219-90882823	HUVEC	blood vessel:	n/a	chr10:90882401-90882409 chr10:90882401-90882410 chr10:90882399-90882411 chr10:90882402-90882409 chr10:90882400-90882410 chr10:90882397-90882408
38	JUN	chr10:90881511-90881759	HepG2	liver:	n/a	chr10:90881637-90881650
39	JUND	chr10:90881466-90881827	HepG2	liver:	n/a	n/a
40	MAFF	chr10:90889786-90890068	HepG2	liver:	n/a	chr10:90889943-90889961
41	MAFK	chr10:90889889-90889919	H1-hESC	embryonic stem cell:	n/a	n/a
42	MAFK	chr10:90889769-90890137	IMR90	lung:	n/a	chr10:90889946-90889957 chr10:90889946-90889966 chr10:90889945-90889960
43	MAFK	chr10:90889850-90890069	HepG2	liver:	n/a	chr10:90889946-90889957 chr10:90889946-90889966 chr10:90889945-90889960
44	MAFK	chr10:90889759-90890082	Hela-S3	cervix:	n/a	chr10:90889946-90889957 chr10:90889946-90889966 chr10:90889945-90889960
45	MAFK	chr10:90889782-90890134	HepG2	liver:	n/a	chr10:90889946-90889957 chr10:90889946-90889966 chr10:90889945-90889960
46	MAX	chr10:90889725-90889984	Hela-S3	cervix:	n/a	n/a
47	MEF2A	chr10:90894707-90895078	GM12878	blood:	n/a	n/a
48	MEF2A	chr10:90894698-90894969	GM12878	blood:	n/a	n/a
49	MEF2C	chr10:90894601-90895124	GM12878	blood:	n/a	chr10:90894866-90894881
50	MXI1	chr10:90889508-90890307	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90879549-90879599	Caco-2	colon:	n/a
2	chr10:90879549-90879599	HCF	heart:	n/a
3	chr10:90879549-90879599	Hepatocyte	liver:	n/a
4	chr10:90879549-90879599	HCM	heart:	n/a
5	chr10:90879549-90879599	HMEC	breast:	n/a
6	chr10:90879549-90879599	HIPEpiC	eye:	n/a
7	chr10:90879549-90879599	SKMC	muscle:	n/a
8	chr10:90879549-90879599	NHDF-neo	bronchial:	n/a
9	chr10:90879549-90879599	HRPEpiC	eye:	n/a
10	chr10:90879549-90879599	AG04449	skin:	fetal
11	chr10:90879549-90879599	K562	blood:	n/a
12	chr10:90879549-90879599	AG04450	lung:	fetal
13	chr10:90879549-90879599	HRCEpiC	kidney:	n/a
14	chr10:90879549-90879599	PFSK-1	brain:	n/a
15	chr10:90879549-90879599	Jurkat	blood:	n/a
16	chr10:90879549-90879599	ProgFib	skin:	n/a
17	chr10:90879549-90879599	RPTEC	kidney:	n/a
18	chr10:90879549-90879599	GM12891	blood:	n/a
19	chr10:90879549-90879599	NB4	blood:	n/a
20	chr10:90879549-90879599	GM12878	blood:	n/a
21	chr10:90879549-90879599	ECC-1	luminal epithelium:	n/a
22	chr10:90879549-90879599	LNCaP	prostate:	n/a
23	chr10:90879549-90879599	IMR90	lung:	fetal
24	chr10:90879549-90879599	HEEpiC	esophagus:	n/a
25	chr10:90879549-90879599	ovcar-3	ovarian:	n/a
26	chr10:90879549-90879599	SK-N-MC	brain:	n/a
27	chr10:90879549-90879599	GM12892	blood:	n/a
28	chr10:90879549-90879599	HPAEpiC	pulmonary alveolar:	n/a
29	chr10:90879549-90879599	AG09319	gingival:	n/a
30	chr10:90879549-90879599	HRE	kidney:	n/a
31	chr10:90879549-90879599	HAEpiC	amniotic membrane:	n/a
32	chr10:90879549-90879599	BE2_C	brain:	n/a
33	chr10:90879549-90879599	AG10803	skin:	n/a
34	chr10:90879549-90879599	U87	brain:	n/a
35	chr10:90879549-90879599	MCF-7	breast:	n/a
36	chr10:90879549-90879599	HEK293	kidney:	embryo
37	chr10:90879549-90879599	MCF10A-Er-Src	breast:	n/a
38	chr10:90879549-90879599	HUVEC	blood vessel:	n/a
39	chr10:90879549-90879599	HNPCEpiC	eye:	n/a
40	chr10:90879549-90879599	PrEC	prostate:	n/a
41	chr10:90879549-90879599	Hela-S3	cervix:	n/a
42	chr10:90879549-90879599	AoSMC	blood vessel:	n/a
43	chr10:90879549-90879599	SK-N-SH_RA	brain:	n/a
44	chr10:90879549-90879599	AG09309	skin:	n/a
45	chr10:90879549-90879599	SK-N-SH	brain:	n/a
46	chr10:90879549-90879599	PANC-1	pancreas:	n/a
47	chr10:90879549-90879599	NH-A	brain:	n/a
48	chr10:90879549-90879599	HepG2	liver:	n/a
49	chr10:90879549-90879599	HL-60	blood:	n/a
50	chr10:90879549-90879599	HCPEpiC	choroid plexus:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAS-4	chr10:90898801-90899215	NONHSAT015500

Variant related genes	Relation type
ENSG00000233292	TF binding region
ENSG00000233292	CpG island

Extended variants
information (count: 539 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1317361	chr10:90879304-90879305	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147508105	chr10:90879384-90879385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113425105	chr10:90879449-90879450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35329380	chr10:90879455-90879456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559546045	chr10:90879456-90879457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111892056	chr10:90879549-90879550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564838026	chr10:90879550-90879551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11202988	chr10:90879563-90879564	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs562108477	chr10:90879610-90879611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531117115	chr10:90879631-90879632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546039020	chr10:90879720-90879721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188055728	chr10:90879737-90879738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72182882	chr10:90879751-90879752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192637385	chr10:90879821-90879822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184479489	chr10:90879936-90879937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568491376	chr10:90879950-90879951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370554498	chr10:90879975-90879976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117415203	chr10:90879978-90879979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549488418	chr10:90879979-90879980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7079258	chr10:90880015-90880016	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs570374323	chr10:90880035-90880036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569235926	chr10:90880043-90880044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113807136	chr10:90880117-90880118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs28533190	chr10:90880127-90880128	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs189283212	chr10:90880155-90880156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112608932	chr10:90880175-90880176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555507748	chr10:90880224-90880225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574688964	chr10:90880274-90880275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573667161	chr10:90880295-90880296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71310984	chr10:90880307-90880308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370800977	chr10:90880310-90880311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34045113	chr10:90880312-90880313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397845073	chr10:90880313-90880314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34882614	chr10:90880318-90880319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112684510	chr10:90880319-90880320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115046345	chr10:90880331-90880332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138445011	chr10:90880336-90880337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182026007	chr10:90880346-90880347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564663520	chr10:90880446-90880447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9420506	chr10:90880457-90880458	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs36095062	chr10:90880459-90880460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7907592	chr10:90880483-90880484	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs562275355	chr10:90880519-90880520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529416494	chr10:90880532-90880533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551048057	chr10:90880533-90880534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72812830	chr10:90880569-90880570	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs113600612	chr10:90880599-90880600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116201063	chr10:90880632-90880633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551777626	chr10:90880650-90880651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370629650	chr10:90880726-90880727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90874600-90879400	Weak transcription	Adipose Nuclei	Adipose
2	chr10:90876200-90883200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr10:90876600-90882200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr10:90878400-90879400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr10:90878400-90880600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr10:90878400-90889600	Weak transcription	NHLF	lung
7	chr10:90878600-90879600	Weak transcription	HSMMtube	muscle
8	chr10:90878600-90880400	Weak transcription	NHDF-Ad	bronchial
9	chr10:90878600-90880600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:90878600-90880600	Weak transcription	Osteobl	bone
11	chr10:90878600-90888000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr10:90878800-90882200	Weak transcription	NHEK	skin
13	chr10:90878800-90888000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr10:90879200-90879800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr10:90879200-90879800	Enhancers	HUVEC	blood vessel
16	chr10:90879200-90880000	Enhancers	HSMM	muscle
17	chr10:90879200-90881400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:90879200-90882000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr10:90879400-90879800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr10:90879400-90881600	Enhancers	Adipose Nuclei	Adipose
21	chr10:90879600-90879800	Enhancers	HSMMtube	muscle
22	chr10:90879600-90880800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr10:90879800-90880200	Weak transcription	HSMMtube	muscle
24	chr10:90879800-90882000	Weak transcription	HUVEC	blood vessel
25	chr10:90879800-90882200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr10:90879800-90882200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr10:90880000-90880400	Weak transcription	HSMM	muscle
28	chr10:90880200-90880600	Enhancers	HSMMtube	muscle
29	chr10:90880400-90881200	Enhancers	HSMM	muscle
30	chr10:90880400-90882800	Enhancers	NHDF-Ad	bronchial
31	chr10:90880600-90881400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr10:90880600-90881400	Enhancers	Osteobl	bone
33	chr10:90880600-90882000	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr10:90880600-90883000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:90880600-90884200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr10:90881200-90881400	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr10:90881400-90882000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr10:90881400-90882200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr10:90881400-90882200	Weak transcription	Osteobl	bone
40	chr10:90881400-90889000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr10:90881600-90882600	Weak transcription	Adipose Nuclei	Adipose
42	chr10:90881800-90882400	Enhancers	Brain Substantia Nigra	brain
43	chr10:90881800-90882600	Enhancers	Brain Cingulate Gyrus	brain
44	chr10:90882000-90882400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr10:90882000-90882800	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr10:90882000-90883000	Enhancers	HUVEC	blood vessel
47	chr10:90882200-90882400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr10:90882200-90882800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr10:90882200-90882800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr10:90882200-90882800	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links