Variant report

Variant	nsv518744
Chromosome Location	chr10:49636507-49643226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:49639893-49640966	K562	blood:	n/a	n/a
2	ARID3A	chr10:49638487-49639028	K562	blood:	n/a	n/a
3	ATF1	chr10:49639968-49640274	K562	blood:	n/a	n/a
4	CEBPB	chr10:49639307-49639418	K562	blood:	n/a	n/a
5	CEBPB	chr10:49638030-49638350	K562	blood:	n/a	n/a
6	CEBPB	chr10:49639905-49640370	K562	blood:	n/a	n/a
7	CEBPB	chr10:49639952-49640326	K562	blood:	n/a	n/a
8	CUX1	chr10:49642752-49642939	K562	blood:	n/a	n/a
9	CUX1	chr10:49638524-49638802	K562	blood:	n/a	n/a
10	CUX1	chr10:49639610-49640413	K562	blood:	n/a	n/a
11	E2F6	chr10:49638653-49639019	K562	blood:	n/a	n/a
12	EP300	chr10:49639895-49640424	K562	blood:	n/a	n/a
13	EP300	chr10:49639043-49639453	K562	blood:	n/a	chr10:49639359-49639367
14	EP300	chr10:49639811-49640991	K562	blood:	n/a	n/a
15	EP300	chr10:49638511-49638983	K562	blood:	n/a	n/a
16	EP300	chr10:49639899-49640369	GM12878	blood:	n/a	n/a
17	GATA2	chr10:49638422-49638921	K562	blood:	n/a	n/a
18	GATA2	chr10:49639865-49640366	K562	blood:	n/a	chr10:49640116-49640125
19	JUND	chr10:49638490-49639243	K562	blood:	n/a	n/a
20	JUND	chr10:49639960-49640275	K562	blood:	n/a	n/a
21	KAP1	chr10:49638944-49639581	K562	blood:	n/a	n/a
22	KAP1	chr10:49640051-49640791	K562	blood:	n/a	n/a
23	MAFF	chr10:49638525-49638725	K562	blood:	n/a	n/a
24	MAX	chr10:49638691-49638987	K562	blood:	n/a	n/a
25	MAX	chr10:49638545-49639020	K562	blood:	n/a	n/a
26	MAX	chr10:49638306-49639020	K562	blood:	n/a	n/a
27	MAZ	chr10:49638633-49639050	K562	blood:	n/a	n/a
28	MXI1	chr10:49638573-49639057	K562	blood:	n/a	n/a
29	MYC	chr10:49638481-49639071	K562	blood:	n/a	n/a
30	MYC	chr10:49639425-49639469	K562	blood:	n/a	n/a
31	MYC	chr10:49638467-49639161	K562	blood:	n/a	n/a
32	NR2F2	chr10:49639828-49640427	K562	blood:	n/a	n/a
33	NR2F2	chr10:49639899-49640323	K562	blood:	n/a	n/a
34	PML	chr10:49639901-49640394	K562	blood:	n/a	n/a
35	POLR2A	chr10:49638532-49639115	U87	brain:	n/a	n/a
36	POLR2A	chr10:49638644-49640544	K562	blood:	n/a	n/a
37	POLR2A	chr10:49642213-49643199	U87	brain:	n/a	n/a
38	POLR2A	chr10:49639979-49640213	K562	blood:	n/a	n/a
39	POLR2A	chr10:49642454-49643104	U87	brain:	n/a	n/a
40	POLR2A	chr10:49639066-49639133	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr10:49640951-49643205	U87	brain:	n/a	n/a
42	POLR2A	chr10:49637955-49638123	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr10:49641163-49643051	K562	blood:	n/a	n/a
44	POLR2A	chr10:49643111-49643414	U87	brain:	n/a	n/a
45	POLR2A	chr10:49642824-49643077	K562	blood:	n/a	n/a
46	POLR2A	chr10:49639801-49640334	U87	brain:	n/a	n/a
47	POLR2A	chr10:49641102-49642035	U87	brain:	n/a	n/a
48	POLR2A	chr10:49641473-49641798	U87	brain:	n/a	n/a
49	POLR2A	chr10:49639801-49640328	U87	brain:	n/a	n/a
50	RCOR1	chr10:49639967-49640295	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49642969-49643019	AG09309	skin:	n/a
2	chr10:49642969-49643019	HUVEC	blood vessel:	n/a
3	chr10:49642969-49643019	SK-N-SH_RA	brain:	n/a
4	chr10:49643086-49643136	CMK	blood:	n/a
5	chr10:49642969-49643019	GM19239	blood:	n/a
6	chr10:49643086-49643136	IMR90	lung:	fetal
7	chr10:49642969-49643019	Hepatocyte	liver:	n/a
8	chr10:49643086-49643136	Hela-S3	cervix:	n/a
9	chr10:49643086-49643136	HEK293	kidney:	embryo
10	chr10:49643086-49643136	AG04449	skin:	fetal
11	chr10:49643086-49643136	HPAEpiC	pulmonary alveolar:	n/a
12	chr10:49642969-49643019	AG09319	gingival:	n/a
13	chr10:49642969-49643019	K562	blood:	n/a
14	chr10:49643086-49643136	SKMC	muscle:	n/a
15	chr10:49643086-49643136	ECC-1	luminal epithelium:	n/a
16	chr10:49642969-49643019	PANC-1	pancreas:	n/a
17	chr10:49643086-49643136	PFSK-1	brain:	n/a
18	chr10:49643086-49643136	HRPEpiC	eye:	n/a
19	chr10:49642969-49643019	Caco-2	colon:	n/a
20	chr10:49642969-49643019	SK-N-SH	brain:	n/a
21	chr10:49642969-49643019	PFSK-1	brain:	n/a
22	chr10:49643086-49643136	HRE	kidney:	n/a
23	chr10:49643086-49643136	AG09319	gingival:	n/a
24	chr10:49643086-49643136	Jurkat	blood:	n/a
25	chr10:49643086-49643136	LNCaP	prostate:	n/a
26	chr10:49642969-49643019	HL-60	blood:	n/a
27	chr10:49643086-49643136	GM06990	blood:	n/a
28	chr10:49642969-49643019	AG04449	skin:	fetal
29	chr10:49642969-49643019	HEK293	kidney:	embryo
30	chr10:49643086-49643136	HIPEpiC	eye:	n/a
31	chr10:49642969-49643019	BJ	skin:	n/a
32	chr10:49642969-49643019	RPTEC	kidney:	n/a
33	chr10:49642969-49643019	HPAEpiC	pulmonary alveolar:	n/a
34	chr10:49642969-49643019	HCPEpiC	choroid plexus:	n/a
35	chr10:49643086-49643136	NB4	blood:	n/a
36	chr10:49642969-49643019	ECC-1	luminal epithelium:	n/a
37	chr10:49642969-49643019	BE2_C	brain:	n/a
38	chr10:49642969-49643019	HCT-116	colon:	n/a
39	chr10:49643086-49643136	Caco-2	colon:	n/a
40	chr10:49643086-49643136	HUVEC	blood vessel:	n/a
41	chr10:49643086-49643136	MCF10A-Er-Src	breast:	n/a
42	chr10:49642969-49643019	SAEC	small airway:	n/a
43	chr10:49642969-49643019	PrEC	prostate:	n/a
44	chr10:49643086-49643136	HNPCEpiC	eye:	n/a
45	chr10:49642969-49643019	A549	lung:	n/a
46	chr10:49643086-49643136	SK-N-MC	brain:	n/a
47	chr10:49643086-49643136	GM19239	blood:	n/a
48	chr10:49642969-49643019	HRCEpiC	kidney:	n/a
49	chr10:49642969-49643019	T-47D	breast:	n/a
50	chr10:49642969-49643019	LNCaP	prostate:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:49631028..49633820-chr10:49635158..49637292,2	MCF-7	breast:
2	chr10:49605751..49608098-chr10:49638652..49640614,2	K562	blood:
3	chr10:49639661..49642619-chr10:49674798..49676427,2	K562	blood:
4	chr10:49514655..49517342-chr10:49637868..49640207,2	K562	blood:
5	chr10:49640741..49644596-chr10:49677175..49679458,3	K562	blood:
6	chr10:49596329..49598626-chr10:49641274..49643307,2	K562	blood:
7	chr10:49513108..49517342-chr10:49638707..49640799,3	K562	blood:
8	chr10:49632219..49636851-chr10:49637055..49643743,11	K562	blood:
9	chr10:49639013..49641362-chr10:49732442..49734428,2	K562	blood:
10	chr10:49589540..49591381-chr10:49641567..49643143,2	K562	blood:
11	chr10:49639954..49642271-chr10:49642777..49645613,2	K562	blood:
12	chr10:49639954..49642271-chr10:49642777..49645613,2	K562	blood:
13	chr10:49628790..49630955-chr10:49635884..49637569,2	K562	blood:
14	chr10:49632219..49636851-chr10:49637055..49643743,11	K562	blood:
15	chr10:49517027..49519236-chr10:49642083..49643882,2	K562	blood:

No data

Variant related genes	Relation type
MAPK8	TF binding region
MAPK8	CpG island
ENSG00000107643	chromatin interactions

Extended variants
information (count: 228 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:228 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4385845	chr10:49636507-49636508	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572732084	chr10:49636526-49636527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs148308174	chr10:49636553-49636554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs12254206	chr10:49636614-49636615	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs79483725	chr10:49636642-49636643	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543133933	chr10:49636657-49636658	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141403945	chr10:49636708-49636709	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs183983466	chr10:49636727-49636728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540577248	chr10:49636747-49636748	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs74446959	chr10:49636750-49636751	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs202221086	chr10:49636795-49636796	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73293518	chr10:49636813-49636814	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551572511	chr10:49636854-49636855	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs199580789	chr10:49636857-49636858	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569727702	chr10:49636863-49636864	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs202076749	chr10:49636866-49636867	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531869537	chr10:49636874-49636875	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550291141	chr10:49636891-49636892	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113544213	chr10:49636903-49636904	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147291525	chr10:49636922-49636923	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554168706	chr10:49636952-49636953	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566379590	chr10:49636990-49636991	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539717367	chr10:49636992-49636993	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs111540494	chr10:49637036-49637037	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140394123	chr10:49637037-49637038	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs140416463	chr10:49637048-49637049	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376293572	chr10:49637049-49637050	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs576549637	chr10:49637091-49637092	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550094450	chr10:49637139-49637140	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142769586	chr10:49637157-49637158	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs144483239	chr10:49637158-49637159	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573358264	chr10:49637166-49637167	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190012616	chr10:49637174-49637175	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs76727362	chr10:49637179-49637180	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533283676	chr10:49637183-49637184	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148414801	chr10:49637198-49637199	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538615702	chr10:49637240-49637241	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563541081	chr10:49637262-49637263	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558540136	chr10:49637287-49637288	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192176024	chr10:49637297-49637298	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs151011899	chr10:49637344-49637345	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535167342	chr10:49637404-49637405	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184492704	chr10:49637414-49637415	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs75440248	chr10:49637424-49637425	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374120857	chr10:49637530-49637531	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs73293521	chr10:49637539-49637540	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs575517214	chr10:49637560-49637561	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190275855	chr10:49637688-49637689	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs137892246	chr10:49637743-49637744	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs61564852	chr10:49637745-49637746	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Thoracic aortic aneurysm	21092924	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
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49607600-49647800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr10:49607600-49652400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:49608000-49645600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr10:49612000-49664200	Weak transcription	Thymus	Thymus
5	chr10:49612800-49660200	Weak transcription	Aorta	Aorta
6	chr10:49614800-49638400	Weak transcription	HUVEC	blood vessel
7	chr10:49619000-49664200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr10:49619600-49645600	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr10:49620600-49643400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr10:49620800-49643400	Weak transcription	Right Ventricle	heart
11	chr10:49620800-49646800	Weak transcription	Hela-S3	cervix
12	chr10:49620800-49647000	Weak transcription	NHDF-Ad	bronchial
13	chr10:49620800-49647600	Weak transcription	Colonic Mucosa	Colon
14	chr10:49620800-49652400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr10:49620800-49658600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr10:49621000-49638400	Weak transcription	Fetal Stomach	stomach
17	chr10:49621000-49638800	Weak transcription	Brain Germinal Matrix	brain
18	chr10:49621200-49638400	Weak transcription	Fetal Muscle Leg	muscle
19	chr10:49621200-49638800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr10:49621200-49641600	Weak transcription	Small Intestine	intestine
21	chr10:49621200-49641800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr10:49621200-49643400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr10:49621200-49647000	Weak transcription	Fetal Intestine Small	intestine
24	chr10:49621200-49647400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr10:49621200-49647800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:49621200-49657400	Weak transcription	Brain Hippocampus Middle	brain
27	chr10:49621400-49637200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr10:49621400-49638000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr10:49621400-49641600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr10:49621400-49641800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr10:49621400-49643600	Weak transcription	Fetal Brain Male	brain
32	chr10:49621400-49644000	Weak transcription	Fetal Brain Female	brain
33	chr10:49621400-49647600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr10:49621400-49650800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr10:49621400-49652200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr10:49621400-49658600	Weak transcription	Brain Substantia Nigra	brain
37	chr10:49621400-49664400	Weak transcription	Brain Angular Gyrus	brain
38	chr10:49621600-49638800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr10:49621600-49643600	Weak transcription	Colon Smooth Muscle	Colon
40	chr10:49621600-49647800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr10:49621600-49652200	Weak transcription	Fetal Heart	heart
42	chr10:49623000-49647000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:49623400-49641400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr10:49623400-49646600	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr10:49624200-49642600	Weak transcription	Fetal Intestine Large	intestine
46	chr10:49624400-49638600	Weak transcription	Fetal Lung	lung
47	chr10:49624600-49664800	Weak transcription	Gastric	stomach
48	chr10:49624800-49638800	Weak transcription	Right Atrium	heart
49	chr10:49625200-49646600	Weak transcription	Osteobl	bone
50	chr10:49625600-49646800	Weak transcription	HSMMtube	muscle

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