Variant report

Variant	nsv895393
Chromosome Location	chr10:52413720-52530819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1433)
CpG islands
(count:1467)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1433 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:52420013-52420185	K562	blood:	n/a	n/a
2	ATF1	chr10:52499751-52500379	K562	blood:	n/a	n/a
3	ATF2	chr10:52499272-52499770	GM12878	blood:	n/a	n/a
4	ATF2	chr10:52499576-52499831	GM12878	blood:	n/a	n/a
5	ATF3	chr10:52499803-52500110	K562	blood:	n/a	n/a
6	BACH1	chr10:52499491-52499981	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:52413762-52414021	K562	blood:	n/a	n/a
8	BATF	chr10:52528646-52528833	GM12878	blood:	n/a	chr10:52528772-52528783
9	BATF	chr10:52483591-52483970	GM12878	blood:	n/a	n/a
10	BATF	chr10:52464214-52464440	GM12878	blood:	n/a	n/a
11	BATF	chr10:52500151-52500419	GM12878	blood:	n/a	chr10:52500262-52500272
12	BATF	chr10:52464232-52464555	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:52483579-52483874	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:52483588-52483995	GM12878	blood:	n/a	n/a
15	BCLAF1	chr10:52499532-52500122	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:52499519-52500222	K562	blood:	n/a	n/a
17	BHLHE40	chr10:52419755-52420219	K562	blood:	n/a	n/a
18	BHLHE40	chr10:52419850-52420189	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:52428723-52428857	K562	blood:	n/a	n/a
20	CBX3	chr10:52461543-52462022	K562	blood:	n/a	n/a
21	CBX3	chr10:52457565-52457966	K562	blood:	n/a	n/a
22	CBX3	chr10:52499171-52500475	K562	blood:	n/a	chr10:52499590-52499601
23	CBX3	chr10:52499234-52500020	K562	blood:	n/a	chr10:52499590-52499601
24	CBX3	chr10:52419780-52420233	K562	blood:	n/a	n/a
25	CBX3	chr10:52419802-52420221	K562	blood:	n/a	n/a
26	CBX3	chr10:52428609-52429004	K562	blood:	n/a	n/a
27	CCNT2	chr10:52499496-52499855	K562	blood:	n/a	n/a
28	CEBPB	chr10:52425983-52426195	K562	blood:	n/a	n/a
29	CEBPB	chr10:52419994-52420182	IMR90	lung:	n/a	n/a
30	CEBPB	chr10:52493141-52493341	K562	blood:	n/a	chr10:52493242-52493253 chr10:52493296-52493307 chr10:52493273-52493284
31	CEBPB	chr10:52419900-52420194	HepG2	liver:	n/a	n/a
32	CEBPB	chr10:52475853-52476055	IMR90	lung:	n/a	chr10:52475994-52476007 chr10:52475995-52476006
33	CEBPB	chr10:52493232-52493370	HepG2	liver:	n/a	chr10:52493242-52493253 chr10:52493296-52493307 chr10:52493273-52493284
34	CEBPB	chr10:52498122-52498408	K562	blood:	n/a	n/a
35	CEBPB	chr10:52475847-52476153	A549	lung:	n/a	chr10:52475994-52476007 chr10:52475995-52476006
36	CEBPB	chr10:52419926-52420201	A549	lung:	n/a	n/a
37	CEBPB	chr10:52475848-52476130	HepG2	liver:	n/a	chr10:52475994-52476007 chr10:52475995-52476006
38	CEBPB	chr10:52475866-52476066	K562	blood:	n/a	chr10:52475994-52476007 chr10:52475995-52476006
39	CEBPB	chr10:52493265-52493366	Hela-S3	cervix:	n/a	chr10:52493296-52493307 chr10:52493273-52493284
40	CEBPB	chr10:52419895-52420206	K562	blood:	n/a	n/a
41	CEBPB	chr10:52419975-52420135	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:52428806-52428914	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPD	chr10:52499550-52499777	HepG2	liver:	n/a	n/a
44	CEBPD	chr10:52499627-52499966	HepG2	liver:	n/a	n/a
45	CEBPD	chr10:52499531-52500112	K562	blood:	n/a	n/a
46	CHD1	chr10:52499351-52499514	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr10:52499507-52499707	GM12878	blood:	n/a	n/a
48	CHD2	chr10:52420008-52420023	K562	blood:	n/a	n/a
49	CHD2	chr10:52420022-52420103	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr10:52419835-52420206	GM12878	blood:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52431183-52431233	NHBE	bronchial:	n/a
2	chr10:52500187-52500237	HCPEpiC	choroid plexus:	n/a
3	chr10:52500425-52500475	ovcar-3	ovarian:	n/a
4	chr10:52431183-52431233	NHBE	bronchial:	n/a
5	chr10:52500187-52500237	HCPEpiC	choroid plexus:	n/a
6	chr10:52500425-52500475	ovcar-3	ovarian:	n/a
7	chr10:52499393-52499443	RPTEC	kidney:	n/a
8	chr10:52499888-52499938	PANC-1	pancreas:	n/a
9	chr10:52502681-52502731	SK-N-SH	brain:	n/a
10	chr10:52500187-52500237	HEEpiC	esophagus:	n/a
11	chr10:52499562-52499612	SK-N-MC	brain:	n/a
12	chr10:52499571-52499621	HCT-116	colon:	n/a
13	chr10:52502681-52502731	HCF	heart:	n/a
14	chr10:52500187-52500237	LNCaP	prostate:	n/a
15	chr10:52434778-52434828	HCPEpiC	choroid plexus:	n/a
16	chr10:52498929-52498979	PFSK-1	brain:	n/a
17	chr10:52433577-52433627	HNPCEpiC	eye:	n/a
18	chr10:52498929-52498979	PrEC	prostate:	n/a
19	chr10:52496341-52496391	MCF-7	breast:	n/a
20	chr10:52434647-52434697	NT2-D1	testis:	n/a
21	chr10:52508516-52508566	IMR90	lung:	fetal
22	chr10:52420019-52420069	PANC-1	pancreas:	n/a
23	chr10:52500020-52500070	AG10803	skin:	n/a
24	chr10:52434552-52434602	SK-N-SH	brain:	n/a
25	chr10:52499562-52499612	BJ	skin:	n/a
26	chr10:52500089-52500139	BJ	skin:	n/a
27	chr10:52487693-52487743	AG09319	gingival:	n/a
28	chr10:52487619-52487669	HCPEpiC	choroid plexus:	n/a
29	chr10:52499393-52499443	IMR90	lung:	fetal
30	chr10:52436125-52436175	SAEC	small airway:	n/a
31	chr10:52487693-52487743	Jurkat	blood:	n/a
32	chr10:52433577-52433627	AG09309	skin:	n/a
33	chr10:52499571-52499621	NHDF-neo	bronchial:	n/a
34	chr10:52420019-52420069	Hela-S3	cervix:	n/a
35	chr10:52498929-52498979	Hepatocyte	liver:	n/a
36	chr10:52420019-52420069	NHBE	bronchial:	n/a
37	chr10:52434552-52434602	K562	blood:	n/a
38	chr10:52499571-52499621	AG04450	lung:	fetal
39	chr10:52500089-52500139	BE2_C	brain:	n/a
40	chr10:52502681-52502731	GM12878	blood:	n/a
41	chr10:52431183-52431233	HAEpiC	amniotic membrane:	n/a
42	chr10:52487693-52487743	HMEC	breast:	n/a
43	chr10:52420019-52420069	SK-N-SH	brain:	n/a
44	chr10:52434552-52434602	SKMC	muscle:	n/a
45	chr10:52433577-52433627	PrEC	prostate:	n/a
46	chr10:52500020-52500070	ECC-1	luminal epithelium:	n/a
47	chr10:52499747-52499797	T-47D	breast:	n/a
48	chr10:52500425-52500475	AoSMC	blood vessel:	n/a
49	chr10:52500425-52500475	SKMC	muscle:	n/a
50	chr10:52487693-52487743	BJ	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:52476123..52479908-chr10:52500945..52503926,3	K562	blood:
2	chr10:52473460..52475005-chr10:52487754..52490480,2	K562	blood:
3	chr10:52495633..52497465-chr10:52497957..52500428,2	K562	blood:
4	chr10:52489655..52491941-chr10:52496784..52498508,2	K562	blood:
5	chr10:52489655..52491941-chr10:52496784..52498508,2	K562	blood:
6	chr10:52476123..52479908-chr10:52500945..52503926,3	K562	blood:
7	chr10:52381243..52386496-chr10:52418227..52421959,6	MCF-7	breast:
8	chr10:52414539..52416441-chr10:52417401..52419945,2	MCF-7	breast:
9	chr10:52389046..52395992-chr10:52408718..52416095,10	K562	blood:
10	chr10:52414539..52416441-chr10:52417401..52419945,2	MCF-7	breast:
11	chr10:52382538..52386733-chr10:52497918..52501112,4	MCF-7	breast:
12	chr10:52473460..52475005-chr10:52487754..52490480,2	K562	blood:
13	chr10:52419903..52420416-chr10:81444547..81445060,2	MCF-7	breast:
14	chr10:52494752..52497133-chr10:52497800..52500428,2	K562	blood:
15	chr10:52382192..52390666-chr10:52409582..52414601,12	MCF-7	breast:
16	chr10:52419698..52420201-chr10:81445043..81445551,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASAH2B-5	chr10:52455352-52455741	NONHSAT013397

No data

Variant related genes	Relation type
NUTM2HP	TF binding region
CTSLP4	TF binding region
ENSG00000231345	TF binding region
PGGT1BP1	TF binding region
ENSG00000226168	TF binding region
ASAH2B	TF binding region
NUTM2HP	CpG island
CTSLP4	CpG island
ENSG00000231345	CpG island
PGGT1BP1	CpG island
ENSG00000226168	CpG island
ASAH2B	CpG island
ENSG00000224886	chromatin interactions
ENSG00000231345	chromatin interactions
ENSG00000226200	chromatin interactions
ENSG00000198964	chromatin interactions
ENSG00000231588	chromatin interactions
ENSG00000204147	chromatin interactions

Extended variants
information (count: 3142 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3142 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3001853	chr10:52413720-52413721	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372303006	chr10:52413729-52413730	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs574179924	chr10:52413730-52413731	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs544774012	chr10:52413799-52413800	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs542849101	chr10:52413848-52413849	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs186680899	chr10:52413857-52413858	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs556917968	chr10:52413863-52413864	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs575088193	chr10:52413871-52413872	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs190298604	chr10:52413882-52413883	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs528738018	chr10:52413890-52413891	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs551631041	chr10:52413929-52413930	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs182580544	chr10:52413932-52413933	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs79711703	chr10:52413934-52413935	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs532753592	chr10:52413940-52413941	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs186811558	chr10:52413951-52413952	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs371659101	chr10:52413961-52413962	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs377179137	chr10:52413963-52413964	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs569650872	chr10:52413973-52413974	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs11006441	chr10:52413974-52413975	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs147840679	chr10:52413983-52413984	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs562339473	chr10:52413986-52413987	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs189702176	chr10:52414030-52414031	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs141460106	chr10:52414042-52414043	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs150284489	chr10:52414057-52414058	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs12247977	chr10:52414117-52414118	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs557475037	chr10:52414175-52414176	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs372547549	chr10:52414182-52414183	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs182538920	chr10:52414185-52414186	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs572270558	chr10:52414202-52414203	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs553172495	chr10:52414232-52414233	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs369615780	chr10:52414243-52414244	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs137914306	chr10:52414254-52414255	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs545306118	chr10:52414263-52414264	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs565193109	chr10:52414280-52414281	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs541678098	chr10:52414284-52414285	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs368302044	chr10:52414291-52414292	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs117887515	chr10:52414320-52414321	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs554918176	chr10:52414326-52414327	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs189246266	chr10:52414345-52414346	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs563435060	chr10:52414355-52414356	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs193060809	chr10:52414375-52414376	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs149043425	chr10:52414395-52414396	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs565900208	chr10:52414404-52414405	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs113846005	chr10:52414408-52414409	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs551705798	chr10:52414436-52414437	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs7904306	chr10:52414456-52414457	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs537494255	chr10:52414472-52414473	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs557063408	chr10:52414479-52414480	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs567622526	chr10:52414512-52414513	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs536363207	chr10:52414515-52414516	Enhancers Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52410000-52413800	Enhancers	Fetal Intestine Large	intestine
2	chr10:52410400-52414800	Enhancers	K562	blood
3	chr10:52411200-52419200	Weak transcription	Fetal Intestine Small	intestine
4	chr10:52411800-52414000	Enhancers	HUVEC	blood vessel
5	chr10:52412200-52414200	Enhancers	Primary B cells from peripheral blood	blood
6	chr10:52412200-52414800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr10:52412800-52413800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr10:52412800-52413800	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr10:52412800-52413800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr10:52412800-52413800	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr10:52412800-52414000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr10:52412800-52414000	Enhancers	Primary T cells from cord blood	blood
13	chr10:52412800-52414000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr10:52412800-52414000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr10:52412800-52414000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr10:52412800-52414000	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr10:52412800-52414200	Enhancers	Adipose Nuclei	Adipose
18	chr10:52412800-52414800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr10:52413000-52413800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr10:52413000-52413800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr10:52413000-52413800	Enhancers	Fetal Thymus	thymus
22	chr10:52413000-52414000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr10:52413200-52414400	Weak transcription	Liver	Liver
24	chr10:52413200-52414400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr10:52413400-52413800	Flanking Active TSS	Primary hematopoietic stem cells	blood
26	chr10:52413400-52414000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr10:52413400-52414000	Enhancers	Primary B cells from cord blood	blood
28	chr10:52413400-52414600	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr10:52413400-52414600	Enhancers	GM12878-XiMat	blood
30	chr10:52413600-52413800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr10:52413600-52413800	Enhancers	Thymus	Thymus
32	chr10:52413600-52414400	Enhancers	Placenta	Placenta
33	chr10:52413600-52414600	Enhancers	Fetal Muscle Leg	muscle
34	chr10:52413600-52419200	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr10:52413600-52419600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr10:52413600-52419600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr10:52413800-52414000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr10:52413800-52414200	Enhancers	Primary hematopoietic stem cells	blood
39	chr10:52413800-52414400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr10:52413800-52418400	Weak transcription	Fetal Thymus	thymus
41	chr10:52413800-52418600	Weak transcription	Fetal Intestine Large	intestine
42	chr10:52413800-52419200	Weak transcription	Thymus	Thymus
43	chr10:52414000-52414600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr10:52414000-52414800	Enhancers	Lung	lung
45	chr10:52414000-52414800	Active TSS	Spleen	Spleen
46	chr10:52414000-52419000	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr10:52414000-52419200	Weak transcription	Primary B cells from cord blood	blood
48	chr10:52414000-52419600	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr10:52414000-52419600	Weak transcription	Primary T cells from cord blood	blood
50	chr10:52414000-52419800	Weak transcription	HUVEC	blood vessel

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