Variant report

Variant	nsv437655
Chromosome Location	chr10:5900973-5910361
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:248)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:248 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5903253-5903873	HepG2	liver:	n/a	chr10:5903606-5903622
2	ATF2	chr10:5904071-5905027	GM12878	blood:	n/a	n/a
3	ATF2	chr10:5904094-5905203	GM12878	blood:	n/a	n/a
4	BATF	chr10:5904206-5904991	GM12878	blood:	n/a	n/a
5	BATF	chr10:5904143-5905100	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:5904162-5905104	GM12878	blood:	n/a	n/a
7	BCL11A	chr10:5904278-5904614	GM12878	blood:	n/a	n/a
8	BCL3	chr10:5904200-5904748	GM12878	blood:	n/a	n/a
9	BCL3	chr10:5903292-5903542	GM12878	blood:	n/a	chr10:5903433-5903442
10	BCLAF1	chr10:5904086-5905107	GM12878	blood:	n/a	n/a
11	BCLAF1	chr10:5904038-5904983	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:5904170-5904892	GM12878	blood:	n/a	n/a
13	CBX3	chr10:5910142-5910480	K562	blood:	n/a	n/a
14	CBX3	chr10:5910103-5910507	K562	blood:	n/a	n/a
15	CBX3	chr10:5907035-5907310	K562	blood:	n/a	n/a
16	CBX3	chr10:5902840-5903782	HCT-116	colon:	n/a	n/a
17	CBX3	chr10:5903296-5903685	HCT-116	colon:	n/a	n/a
18	CEBPB	chr10:5902969-5903165	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:5904056-5904980	GM12878	blood:	n/a	n/a
20	CEBPB	chr10:5904144-5904329	HepG2	liver:	n/a	n/a
21	CEBPB	chr10:5909319-5909454	K562	blood:	n/a	n/a
22	CEBPB	chr10:5904286-5904770	GM12878	blood:	n/a	n/a
23	CEBPB	chr10:5903382-5903397	HepG2	liver:	n/a	n/a
24	CHD1	chr10:5904267-5904867	GM12878	blood:	n/a	n/a
25	CHD2	chr10:5904177-5905077	GM12878	blood:	n/a	n/a
26	CREB1	chr10:5904075-5905144	GM12878	blood:	n/a	n/a
27	CREB1	chr10:5904117-5905044	GM12878	blood:	n/a	n/a
28	CTCF	chr10:5905160-5905310	HCT-116	colon:	n/a	n/a
29	CTCF	chr10:5905020-5905170	HepG2	liver:	n/a	n/a
30	CTCF	chr10:5905100-5905250	A549	lung:	n/a	n/a
31	CTCF	chr10:5905080-5905230	HFF	foreskin:	n/a	n/a
32	CTCF	chr10:5905080-5905230	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr10:5905132-5905212	HepG2	liver:	n/a	n/a
34	CTCF	chr10:5905100-5905250	GM12868	blood:	n/a	n/a
35	CTCF	chr10:5905100-5905250	GM12873	blood:	n/a	n/a
36	CTCF	chr10:5905100-5905250	GM12871	blood:	n/a	n/a
37	CTCF	chr10:5909954-5909984	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr10:5905100-5905250	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr10:5905060-5905210	HVMF	connective:	n/a	n/a
40	CTCF	chr10:5905116-5905183	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr10:5909760-5909910	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:5904483-5905254	GM12878	blood:	n/a	n/a
43	CTCF	chr10:5905040-5905190	AG04449	skin:	n/a	n/a
44	CTCF	chr10:5905020-5905170	HEK293	kidney:	n/a	n/a
45	CTCF	chr10:5905020-5905170	RPTEC	kidney:	n/a	n/a
46	CTCF	chr10:5905160-5905310	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr10:5905100-5905250	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr10:5905040-5905190	HMF	breast:	n/a	n/a
49	CUX1	chr10:5904260-5904824	GM12878	blood:	n/a	n/a
50	E2F4	chr10:5903259-5903609	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5904561-5904611	CMK	blood:	n/a
2	chr10:5904561-5904611	H1-hESC	embryonic stem cell:	embryo
3	chr10:5904561-5904611	Caco-2	colon:	n/a
4	chr10:5904561-5904611	HRCEpiC	kidney:	n/a
5	chr10:5904561-5904611	SK-N-SH_RA	brain:	n/a
6	chr10:5904561-5904611	AG09309	skin:	n/a
7	chr10:5904561-5904611	HNPCEpiC	eye:	n/a
8	chr10:5904561-5904611	HRPEpiC	eye:	n/a
9	chr10:5904561-5904611	HPAEpiC	pulmonary alveolar:	n/a
10	chr10:5904561-5904611	PrEC	prostate:	n/a
11	chr10:5904561-5904611	ProgFib	skin:	n/a
12	chr10:5904561-5904611	HL-60	blood:	n/a
13	chr10:5904561-5904611	A549	lung:	n/a
14	chr10:5904561-5904611	HCM	heart:	n/a
15	chr10:5904561-5904611	GM12892	blood:	n/a
16	chr10:5904561-5904611	Jurkat	blood:	n/a
17	chr10:5904561-5904611	PFSK-1	brain:	n/a
18	chr10:5904561-5904611	AoSMC	blood vessel:	n/a
19	chr10:5904561-5904611	ovcar-3	ovarian:	n/a
20	chr10:5904561-5904611	Hela-S3	cervix:	n/a
21	chr10:5904561-5904611	HepG2	liver:	n/a
22	chr10:5904561-5904611	AG04449	skin:	fetal
23	chr10:5904561-5904611	HCPEpiC	choroid plexus:	n/a
24	chr10:5904561-5904611	T-47D	breast:	n/a
25	chr10:5904561-5904611	MCF10A-Er-Src	breast:	n/a
26	chr10:5904561-5904611	HCF	heart:	n/a
27	chr10:5904561-5904611	PANC-1	pancreas:	n/a
28	chr10:5904561-5904611	SK-N-MC	brain:	n/a
29	chr10:5904561-5904611	AG10803	skin:	n/a
30	chr10:5904561-5904611	HUVEC	blood vessel:	n/a
31	chr10:5904561-5904611	NB4	blood:	n/a
32	chr10:5904561-5904611	NH-A	brain:	n/a
33	chr10:5904561-5904611	Hepatocyte	liver:	n/a
34	chr10:5904561-5904611	RPTEC	kidney:	n/a
35	chr10:5904561-5904611	HMEC	breast:	n/a
36	chr10:5904561-5904611	MCF-7	breast:	n/a
37	chr10:5904561-5904611	AG09319	gingival:	n/a
38	chr10:5904561-5904611	HAEpiC	amniotic membrane:	n/a
39	chr10:5904561-5904611	IMR90	lung:	fetal
40	chr10:5904561-5904611	HRE	kidney:	n/a
41	chr10:5904561-5904611	HEK293	kidney:	embryo
42	chr10:5904561-5904611	NT2-D1	testis:	n/a
43	chr10:5904561-5904611	SK-N-SH	brain:	n/a
44	chr10:5904561-5904611	HEEpiC	esophagus:	n/a
45	chr10:5904561-5904611	GM12878	blood:	n/a
46	chr10:5904561-5904611	AG04450	lung:	fetal
47	chr10:5904561-5904611	NHDF-neo	bronchial:	n/a
48	chr10:5904561-5904611	ECC-1	luminal epithelium:	n/a
49	chr10:5904561-5904611	BE2_C	brain:	n/a
50	chr10:5904561-5904611	U87	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5910337..5913057-chr10:5913896..5915551,2	K562	blood:
2	chr10:5910241..5913072-chr10:5913979..5917301,3	MCF-7	breast:
3	chr10:5903402..5905306-chr10:5930976..5933543,3	MCF-7	breast:
4	chr10:5853575..5857221-chr10:5900529..5905112,5	MCF-7	breast:
5	chr10:5853453..5856522-chr10:5901378..5904221,3	K562	blood:
6	chr10:5904346..5907644-chr10:5928919..5931742,3	MCF-7	breast:
7	chr10:5900731..5902492-chr10:5915568..5917160,2	K562	blood:
8	chr10:5902878..5905797-chr10:5909283..5911826,2	MCF-7	breast:
9	chr10:5852752..5856561-chr10:5907945..5911516,4	MCF-7	breast:
10	chr10:5850597..5856224-chr10:5899689..5902412,5	K562	blood:
11	chr10:5850597..5853484-chr10:5898526..5901196,3	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDI2-2	chr10:5904161-5904557	NONHSAT011187
2	lnc-GDI2-2	chr10:5903768-5903859	NONHSAT011187

No data

Variant related genes	Relation type
ENSG00000240180	TF binding region
ENSG00000240180	CpG island
ENSG00000272764	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000240180	chromatin interactions
ENSG00000134461	chromatin interactions

Extended variants
information (count: 424 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:424 , 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	rs907689	chr10:5900973-5900974	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77880346	chr10:5901060-5901061	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554535168	chr10:5901066-5901067	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs576271752	chr10:5901102-5901103	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74961712	chr10:5901108-5901109	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569712152	chr10:5901121-5901122	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs112432040	chr10:5901124-5901125	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs78782013	chr10:5901127-5901128	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs558367874	chr10:5901128-5901129	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs370375709	chr10:5901150-5901151	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559028204	chr10:5901161-5901162	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs180677652	chr10:5901164-5901165	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs151064602	chr10:5901180-5901181	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs373768889	chr10:5901186-5901187	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569576983	chr10:5901220-5901221	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs578191652	chr10:5901300-5901301	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs552944446	chr10:5901304-5901305	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs140935375	chr10:5901366-5901367	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs907690	chr10:5901367-5901368	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs553473324	chr10:5901377-5901378	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs200685201	chr10:5901393-5901394	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs368477533	chr10:5901396-5901397	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs111796926	chr10:5901402-5901403	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs71479742	chr10:5901403-5901404	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs540492294	chr10:5901407-5901408	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535611253	chr10:5901408-5901409	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs58202209	chr10:5901409-5901410	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs368561750	chr10:5901410-5901411	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs557305220	chr10:5901413-5901414	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs150203108	chr10:5901418-5901419	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs184916668	chr10:5901425-5901426	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs558437819	chr10:5901466-5901467	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112191967	chr10:5901512-5901513	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs116436037	chr10:5901526-5901527	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs112791945	chr10:5901550-5901551	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547937650	chr10:5901569-5901570	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs111497123	chr10:5901616-5901617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs563285820	chr10:5901631-5901632	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77025915	chr10:5901633-5901634	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs113681254	chr10:5901670-5901671	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs530430813	chr10:5901675-5901676	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs370450160	chr10:5901689-5901690	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373633639	chr10:5901702-5901703	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs113787358	chr10:5901707-5901708	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372596268	chr10:5901708-5901709	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs541992393	chr10:5901748-5901749	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs182065707	chr10:5901779-5901780	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs568591052	chr10:5901811-5901812	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs367567277	chr10:5901823-5901824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs386740394	chr10:5901824-5901825	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	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
Breast cancer	17133270	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	22522925	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:210 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5888800-5904400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr10:5889400-5902000	Weak transcription	Placenta	Placenta
3	chr10:5894600-5908600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr10:5894600-5908600	Weak transcription	K562	blood
5	chr10:5894600-5916800	Weak transcription	Spleen	Spleen
6	chr10:5896200-5912200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr10:5896400-5918200	Weak transcription	Fetal Lung	lung
8	chr10:5896600-5902000	Weak transcription	Fetal Muscle Leg	muscle
9	chr10:5896600-5903800	Weak transcription	Fetal Stomach	stomach
10	chr10:5897000-5903800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr10:5898400-5901000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:5899000-5904200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr10:5899200-5903000	Weak transcription	HepG2	liver
14	chr10:5899800-5901200	Enhancers	Brain Angular Gyrus	brain
15	chr10:5899800-5901400	Enhancers	Brain Hippocampus Middle	brain
16	chr10:5899800-5904200	Weak transcription	Ovary	ovary
17	chr10:5899800-5905000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr10:5900000-5904000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr10:5900000-5916600	Weak transcription	Pancreas	Pancrea
20	chr10:5900400-5901200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr10:5900400-5901800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr10:5900400-5916200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr10:5900600-5901000	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr10:5900600-5902000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr10:5900600-5916200	Weak transcription	Stomach Smooth Muscle	stomach
26	chr10:5900800-5901000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:5900800-5901000	Active TSS	Gastric	stomach
28	chr10:5900800-5901200	Flanking Active TSS	Brain Anterior Caudate	brain
29	chr10:5900800-5901200	Flanking Active TSS	Brain Cingulate Gyrus	brain
30	chr10:5900800-5902000	Weak transcription	Brain Substantia Nigra	brain
31	chr10:5900800-5910600	Weak transcription	Brain Germinal Matrix	brain
32	chr10:5901000-5901200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr10:5901000-5901200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
34	chr10:5901000-5904200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr10:5901000-5916600	Weak transcription	Gastric	stomach
36	chr10:5901200-5901600	Enhancers	Brain Anterior Caudate	brain
37	chr10:5901200-5901600	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr10:5901200-5903200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:5901200-5903200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr10:5901200-5904200	Weak transcription	Brain Angular Gyrus	brain
41	chr10:5901200-5918200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:5901400-5905000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:5901400-5915200	Weak transcription	Brain Hippocampus Middle	brain
44	chr10:5901600-5904200	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr10:5901600-5912600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr10:5901600-5915600	Weak transcription	Brain Anterior Caudate	brain
47	chr10:5901800-5902400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr10:5901800-5904200	Weak transcription	Fetal Intestine Small	intestine
49	chr10:5901800-5910800	Weak transcription	Fetal Brain Female	brain
50	chr10:5902000-5902200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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