Variant report

Variant	nsv975002
Chromosome Location	chr10:691542-699487
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	chr10:695549-696087	HepG2	liver:	n/a	n/a
2	ATF1	chr10:691655-691733	K562	blood:	n/a	n/a
3	BHLHE40	chr10:695485-697003	HepG2	liver:	n/a	n/a
4	BHLHE40	chr10:695707-696007	HepG2	liver:	n/a	n/a
5	CEBPB	chr10:695464-696050	IMR90	lung:	n/a	n/a
6	CEBPB	chr10:695403-696085	HepG2	liver:	n/a	n/a
7	CEBPB	chr10:697228-697554	IMR90	lung:	n/a	n/a
8	CEBPB	chr10:695684-696164	HepG2	liver:	n/a	n/a
9	CEBPB	chr10:695388-696030	A549	lung:	n/a	n/a
10	CEBPD	chr10:695811-696058	HepG2	liver:	n/a	n/a
11	CEBPD	chr10:695785-696331	HepG2	liver:	n/a	n/a
12	CREB1	chr10:695565-696794	HepG2	liver:	n/a	n/a
13	CREB1	chr10:695682-696078	A549	lung:	n/a	n/a
14	CREB1	chr10:695734-695984	A549	lung:	n/a	n/a
15	CREB1	chr10:695672-696183	HepG2	liver:	n/a	n/a
16	CTCF	chr10:698800-698950	MCF-7	breast:	n/a	n/a
17	CTCF	chr10:693878-693957	GM13976	blood:	n/a	n/a
18	CTCF	chr10:694301-694378	GM19239	blood:	n/a	n/a
19	ELF1	chr10:695777-696007	HepG2	liver:	n/a	n/a
20	ELF1	chr10:695680-696083	HepG2	liver:	n/a	n/a
21	EP300	chr10:695726-696137	HepG2	liver:	n/a	chr10:695903-695912 chr10:695896-695910 chr10:695984-696000 chr10:695902-695916
22	EP300	chr10:695478-696062	HepG2	liver:	n/a	chr10:695903-695912 chr10:695896-695910 chr10:695984-696000 chr10:695902-695916
23	FOSL2	chr10:695674-696085	HepG2	liver:	n/a	n/a
24	FOXA1	chr10:695647-696197	HepG2	liver:	n/a	n/a
25	FOXA1	chr10:695677-696189	HepG2	liver:	n/a	n/a
26	FOXA1	chr10:695712-696170	HepG2	liver:	n/a	n/a
27	FOXA1	chr10:695712-696200	HepG2	liver:	n/a	n/a
28	FOXA2	chr10:695723-696364	A549	lung:	n/a	n/a
29	FOXA2	chr10:695734-696107	HepG2	liver:	n/a	n/a
30	FOXP2	chr10:695783-696020	PFSK-1	brain:	n/a	n/a
31	GABPA	chr10:695675-696109	A549	lung:	n/a	n/a
32	GABPA	chr10:695792-695999	HepG2	liver:	n/a	n/a
33	GATA2	chr10:691583-691975	HUVEC	blood vessel:	n/a	n/a
34	HDAC2	chr10:695685-696029	HepG2	liver:	n/a	n/a
35	HEY1	chr10:695735-696239	HepG2	liver:	n/a	n/a
36	HEY1	chr10:695839-696140	HepG2	liver:	n/a	n/a
37	HNF4A	chr10:695691-696654	HepG2	liver:	n/a	chr10:695927-695942 chr10:695928-695941 chr10:695927-695941 chr10:695925-695943 chr10:695927-695942 chr10:695929-695941 chr10:695926-695941 chr10:695928-695940 chr10:695927-695941
38	HNF4A	chr10:695644-696174	HepG2	liver:	n/a	chr10:695927-695942 chr10:695928-695941 chr10:695927-695941 chr10:695925-695943 chr10:695927-695942 chr10:695929-695941 chr10:695926-695941 chr10:695928-695940 chr10:695927-695941
39	HNF4A	chr10:695726-696322	HepG2	liver:	n/a	chr10:695927-695942 chr10:695928-695941 chr10:695927-695941 chr10:695925-695943 chr10:695927-695942 chr10:695929-695941 chr10:695926-695941 chr10:695928-695940 chr10:695927-695941
40	HNF4G	chr10:695694-696083	HepG2	liver:	n/a	chr10:695927-695942 chr10:695928-695941 chr10:695927-695941 chr10:695925-695943 chr10:695927-695942 chr10:695929-695941 chr10:695928-695940 chr10:695927-695941
41	JUND	chr10:695730-696011	HepG2	liver:	n/a	n/a
42	MAFK	chr10:695813-696098	HepG2	liver:	n/a	n/a
43	MAX	chr10:695617-696863	HepG2	liver:	n/a	chr10:696594-696609 chr10:696514-696523 chr10:696595-696606
44	MAX	chr10:695712-696740	HepG2	liver:	n/a	chr10:696594-696609 chr10:696514-696523 chr10:696595-696606
45	MAX	chr10:695799-696054	A549	lung:	n/a	n/a
46	MAX	chr10:695543-696974	HepG2	liver:	n/a	chr10:696594-696609 chr10:696514-696523 chr10:696595-696606
47	MAZ	chr10:695508-696192	HepG2	liver:	n/a	n/a
48	MXI1	chr10:695726-696782	HepG2	liver:	n/a	n/a
49	MYC	chr10:696518-696537	HepG2	liver:	n/a	n/a
50	MYC	chr10:693839-693958	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:697055-697105	A549	lung:	n/a
2	chr10:695877-695927	SAEC	small airway:	n/a
3	chr10:693439-693489	AG09309	skin:	n/a
4	chr10:697055-697105	A549	lung:	n/a
5	chr10:695877-695927	SAEC	small airway:	n/a
6	chr10:693439-693489	AG09309	skin:	n/a
7	chr10:698258-698308	HCPEpiC	choroid plexus:	n/a
8	chr10:696356-696406	HL-60	blood:	n/a
9	chr10:696356-696406	NHBE	bronchial:	n/a
10	chr10:697901-697951	NB4	blood:	n/a
11	chr10:696063-696113	HMEC	breast:	n/a
12	chr10:695900-695950	HCPEpiC	choroid plexus:	n/a
13	chr10:693439-693489	K562	blood:	n/a
14	chr10:696356-696406	ProgFib	skin:	n/a
15	chr10:694058-694108	K562	blood:	n/a
16	chr10:697901-697951	NHBE	bronchial:	n/a
17	chr10:697840-697890	HCPEpiC	choroid plexus:	n/a
18	chr10:695900-695950	HMEC	breast:	n/a
19	chr10:695900-695950	Jurkat	blood:	n/a
20	chr10:695301-695351	HEEpiC	esophagus:	n/a
21	chr10:696332-696382	CMK	blood:	n/a
22	chr10:697055-697105	HepG2	liver:	n/a
23	chr10:697901-697951	GM06990	blood:	n/a
24	chr10:695301-695351	Caco-2	colon:	n/a
25	chr10:695853-695903	HAEpiC	amniotic membrane:	n/a
26	chr10:696321-696371	RPTEC	kidney:	n/a
27	chr10:694058-694108	H1-hESC	embryonic stem cell:	embryo
28	chr10:695877-695927	HCM	heart:	n/a
29	chr10:695859-695909	GM06990	blood:	n/a
30	chr10:697771-697821	GM12891	blood:	n/a
31	chr10:697055-697105	HUVEC	blood vessel:	n/a
32	chr10:693439-693489	NH-A	brain:	n/a
33	chr10:695853-695903	NH-A	brain:	n/a
34	chr10:696356-696406	HCF	heart:	n/a
35	chr10:698258-698308	CMK	blood:	n/a
36	chr10:695301-695351	GM19239	blood:	n/a
37	chr10:697055-697105	GM19239	blood:	n/a
38	chr10:695853-695903	PANC-1	pancreas:	n/a
39	chr10:695844-695894	Caco-2	colon:	n/a
40	chr10:693439-693489	GM06990	blood:	n/a
41	chr10:696063-696113	HIPEpiC	eye:	n/a
42	chr10:697840-697890	AG04449	skin:	fetal
43	chr10:697055-697105	BE2_C	brain:	n/a
44	chr10:696321-696371	SK-N-MC	brain:	n/a
45	chr10:693439-693489	NHBE	bronchial:	n/a
46	chr10:695900-695950	GM12878	blood:	n/a
47	chr10:697840-697890	AG09309	skin:	n/a
48	chr10:698258-698308	H1-hESC	embryonic stem cell:	embryo
49	chr10:697840-697890	AG04450	lung:	fetal
50	chr10:696356-696406	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:691751..694285-chr10:694356..695999,2	K562	blood:
2	chr10:698785..701781-chr10:833421..835495,2	MCF-7	breast:
3	chr10:692996..695820-chr10:700101..701896,2	MCF-7	breast:
4	chr10:692009..694331-chr10:706518..708449,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf108-1	chr10:696231-696382	NONHSAT010867
2	lnc-C10orf108-1	chr10:696017-696382	NR_027152
3	lnc-C10orf108-1	chr10:697051-698595	NONHSAT010867
4	lnc-C10orf108-1	chr10:695888-696118	NONHSAT010867

Variant related genes	Relation type
MIR5699	TF binding region
PRR26	TF binding region
MIR5699	CpG island
PRR26	CpG island
ENSG00000180525	chromatin interactions

Extended variants
information (count: 448 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75481146	chr10:691568-691569	Weak transcription ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs560303110	chr10:691631-691632	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs550908794	chr10:691692-691693	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs531947887	chr10:691709-691710	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs190509300	chr10:691732-691733	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs142442104	chr10:691744-691745	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs529360291	chr10:691745-691746	Weak transcription ZNF genes & repeats Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs566822970	chr10:691751-691752	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs549214340	chr10:691764-691765	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs145952711	chr10:691773-691774	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs575734349	chr10:691779-691780	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs537336416	chr10:691810-691811	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs79800231	chr10:691814-691815	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs573884959	chr10:691841-691842	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs181752698	chr10:691880-691881	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs542331065	chr10:691933-691934	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs559516310	chr10:692011-692012	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572837441	chr10:692016-692017	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568995055	chr10:692034-692035	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10904533	chr10:692112-692113	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs186782192	chr10:692153-692154	Weak transcription Enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs530463527	chr10:692185-692186	Weak transcription Enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs371142256	chr10:692222-692223	Weak transcription Enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs369534280	chr10:692253-692254	Weak transcription Enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs550170064	chr10:692307-692308	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561374590	chr10:692344-692345	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188734800	chr10:692403-692404	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75053567	chr10:692410-692411	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs139463585	chr10:692411-692412	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181170536	chr10:692435-692436	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532476578	chr10:692439-692440	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149655219	chr10:692440-692441	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569386042	chr10:692527-692528	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538197625	chr10:692528-692529	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185201342	chr10:692539-692540	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567415548	chr10:692552-692553	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536584313	chr10:692561-692562	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552872109	chr10:692589-692590	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs114873172	chr10:692763-692764	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544694462	chr10:692814-692815	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs527687366	chr10:692847-692848	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs548774529	chr10:692918-692919	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574997976	chr10:692934-692935	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs189624975	chr10:692936-692937	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs560953175	chr10:692944-692945	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs182700590	chr10:692945-692946	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs202160478	chr10:692964-692965	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs530310667	chr10:692977-692978	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs369764391	chr10:692983-692984	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs55740599	chr10:692999-693000	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:672000-700000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:672600-695800	Weak transcription	NHLF	lung
3	chr10:681800-696200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr10:683000-696000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr10:684200-700000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr10:685600-699800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr10:685800-695200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr10:686200-696200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr10:687400-700000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr10:687600-695200	Weak transcription	Right Ventricle	heart
11	chr10:688800-693400	Weak transcription	Pancreas	Pancrea
12	chr10:688800-694400	Weak transcription	Gastric	stomach
13	chr10:688800-698200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:688800-702600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr10:689200-696000	Weak transcription	Psoas Muscle	Psoas
16	chr10:690000-691600	ZNF genes & repeats	Fetal Stomach	stomach
17	chr10:690400-691600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:690400-691600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr10:690600-691600	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
20	chr10:690600-692000	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
21	chr10:690800-691800	ZNF genes & repeats	Brain Substantia Nigra	brain
22	chr10:691200-692000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:691200-695600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr10:691200-704200	Weak transcription	HSMM	muscle
25	chr10:691200-704800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr10:691400-691600	Weak transcription	Osteobl	bone
27	chr10:691400-691800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr10:691400-691800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr10:691400-692000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr10:691400-692000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr10:691400-692000	Weak transcription	Right Atrium	heart
32	chr10:691400-694800	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr10:691400-695000	Weak transcription	Colon Smooth Muscle	Colon
34	chr10:691400-695200	Weak transcription	Brain Hippocampus Middle	brain
35	chr10:691400-695200	Weak transcription	Fetal Lung	lung
36	chr10:691400-695800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr10:691400-695800	Weak transcription	Brain Angular Gyrus	brain
38	chr10:691400-695800	Weak transcription	Fetal Muscle Trunk	muscle
39	chr10:691400-695800	Weak transcription	Left Ventricle	heart
40	chr10:691400-704200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr10:691600-692000	Enhancers	HUVEC	blood vessel
42	chr10:691600-694200	Weak transcription	Esophagus	oesophagus
43	chr10:691600-695600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr10:691600-695600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr10:691800-692000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr10:691800-692200	Weak transcription	Brain Cingulate Gyrus	brain
47	chr10:691800-692200	Weak transcription	Fetal Muscle Leg	muscle
48	chr10:691800-692800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr10:691800-695200	Weak transcription	Brain Substantia Nigra	brain
50	chr10:692000-692400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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