Variant report

Variant	nsv831872
Chromosome Location	chr10:52663328-52818537
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	chr10:52770729-52770929	HepG2	liver:	n/a	n/a
2	BACH1	chr10:52751182-52751853	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr10:52750092-52750699	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr10:52689519-52689740	GM12878	blood:	n/a	chr10:52689618-52689629 chr10:52689619-52689629 chr10:52689615-52689625
5	BATF	chr10:52689505-52689693	GM12878	blood:	n/a	chr10:52689618-52689629 chr10:52689619-52689629 chr10:52689615-52689625
6	BCL11A	chr10:52795098-52795411	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr10:52770708-52770927	GM12878	blood:	n/a	n/a
8	BRCA1	chr10:52751262-52751294	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr10:52683256-52683609	K562	blood:	n/a	n/a
10	CBX3	chr10:52683245-52683563	K562	blood:	n/a	n/a
11	CCNT2	chr10:52674565-52674571	K562	blood:	n/a	n/a
12	CEBPB	chr10:52774462-52774964	IMR90	lung:	n/a	n/a
13	CEBPB	chr10:52741167-52741509	IMR90	lung:	n/a	chr10:52741338-52741349 chr10:52741338-52741347 chr10:52741338-52741347 chr10:52741338-52741347 chr10:52741336-52741349 chr10:52741338-52741347 chr10:52741336-52741347
14	CEBPB	chr10:52816909-52817121	HepG2	liver:	n/a	chr10:52817043-52817054 chr10:52817042-52817053 chr10:52817044-52817053
15	CEBPB	chr10:52737916-52738034	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:52678773-52679148	MCF-7	breast:	n/a	n/a
17	CEBPB	chr10:52678862-52679132	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr10:52741159-52741462	HepG2	liver:	n/a	chr10:52741338-52741349 chr10:52741338-52741347 chr10:52741338-52741347 chr10:52741338-52741347 chr10:52741336-52741349 chr10:52741338-52741347 chr10:52741336-52741347
19	CEBPB	chr10:52750382-52750701	IMR90	lung:	n/a	n/a
20	CEBPB	chr10:52791583-52791783	H1-hESC	embryonic stem cell:	n/a	chr10:52791705-52791718 chr10:52791706-52791717
21	CEBPB	chr10:52787090-52787268	A549	lung:	n/a	chr10:52787196-52787207 chr10:52787198-52787209 chr10:52787196-52787209
22	CEBPB	chr10:52816932-52817206	IMR90	lung:	n/a	chr10:52817043-52817054 chr10:52817042-52817053 chr10:52817044-52817053
23	CEBPB	chr10:52668331-52668442	HepG2	liver:	n/a	chr10:52668357-52668368
24	CEBPB	chr10:52787065-52787265	HepG2	liver:	n/a	chr10:52787196-52787207 chr10:52787198-52787209 chr10:52787196-52787209
25	CEBPB	chr10:52678801-52679164	IMR90	lung:	n/a	n/a
26	CEBPB	chr10:52753546-52753835	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:52791586-52791795	HepG2	liver:	n/a	chr10:52791705-52791718 chr10:52791706-52791717
28	CEBPB	chr10:52678891-52679113	K562	blood:	n/a	n/a
29	CEBPB	chr10:52758957-52759286	IMR90	lung:	n/a	n/a
30	CEBPB	chr10:52787063-52787304	IMR90	lung:	n/a	chr10:52787196-52787207 chr10:52787198-52787209 chr10:52787196-52787209
31	CEBPB	chr10:52760090-52760102	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr10:52807306-52807523	IMR90	lung:	n/a	n/a
33	CEBPB	chr10:52741217-52741494	K562	blood:	n/a	chr10:52741338-52741349 chr10:52741338-52741347 chr10:52741338-52741347 chr10:52741338-52741347 chr10:52741336-52741349 chr10:52741338-52741347 chr10:52741336-52741347
34	CEBPB	chr10:52678793-52679147	A549	lung:	n/a	n/a
35	CEBPB	chr10:52797776-52798103	IMR90	lung:	n/a	n/a
36	CEBPB	chr10:52741242-52741412	A549	lung:	n/a	chr10:52741338-52741349 chr10:52741338-52741347 chr10:52741338-52741347 chr10:52741338-52741347 chr10:52741336-52741349 chr10:52741338-52741347 chr10:52741336-52741347
37	CEBPB	chr10:52759894-52760318	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:52791653-52791764	K562	blood:	n/a	chr10:52791705-52791718 chr10:52791706-52791717
39	CEBPB	chr10:52797803-52798077	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:52678802-52679143	HepG2	liver:	n/a	n/a
41	CHD1	chr10:52751226-52751326	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr10:52771006-52771031	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr10:52761480-52761630	HA-sp	spinal cord:	n/a	chr10:52761553-52761569 chr10:52761554-52761575 chr10:52761552-52761570
44	CTCF	chr10:52697360-52697510	HAc	cerebellar:	n/a	chr10:52697482-52697490 chr10:52697479-52697500 chr10:52697477-52697495 chr10:52697478-52697494
45	CTCF	chr10:52807700-52807850	MCF-7	breast:	n/a	chr10:52807814-52807835
46	CTCF	chr10:52770770-52770938	ECC-1	luminal epithelium:	n/a	n/a
47	CTCF	chr10:52807740-52807890	AG09309	skin:	n/a	chr10:52807814-52807835
48	CTCF	chr10:52761460-52761610	SK-N-SH_RA	brain:	n/a	chr10:52761553-52761569 chr10:52761554-52761575 chr10:52761552-52761570
49	CTCF	chr10:52697153-52697203	Fibrobl	skin:	n/a	n/a
50	CTCF	chr10:52752080-52752230	HCPEpiC	choroid plexus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52752476-52752526	HepG2	liver:	n/a
2	chr10:52750743-52750793	U87	brain:	n/a
3	chr10:52750296-52750346	AG04449	skin:	fetal
4	chr10:52752476-52752526	HepG2	liver:	n/a
5	chr10:52750743-52750793	U87	brain:	n/a
6	chr10:52750296-52750346	AG04449	skin:	fetal
7	chr10:52750296-52750346	ECC-1	luminal epithelium:	n/a
8	chr10:52751341-52751391	GM12892	blood:	n/a
9	chr10:52765418-52765468	GM12891	blood:	n/a
10	chr10:52751119-52751169	Caco-2	colon:	n/a
11	chr10:52750754-52750804	PANC-1	pancreas:	n/a
12	chr10:52750754-52750804	SK-N-SH_RA	brain:	n/a
13	chr10:52754927-52754977	ovcar-3	ovarian:	n/a
14	chr10:52751341-52751391	NT2-D1	testis:	n/a
15	chr10:52751341-52751391	HNPCEpiC	eye:	n/a
16	chr10:52765418-52765468	SK-N-SH	brain:	n/a
17	chr10:52750296-52750346	HL-60	blood:	n/a
18	chr10:52751764-52751814	PrEC	prostate:	n/a
19	chr10:52751764-52751814	AoSMC	blood vessel:	n/a
20	chr10:52750296-52750346	HRPEpiC	eye:	n/a
21	chr10:52750743-52750793	K562	blood:	n/a
22	chr10:52765418-52765468	RPTEC	kidney:	n/a
23	chr10:52750930-52750980	NT2-D1	testis:	n/a
24	chr10:52747890-52747940	NHBE	bronchial:	n/a
25	chr10:52751341-52751391	NB4	blood:	n/a
26	chr10:52750296-52750346	PANC-1	pancreas:	n/a
27	chr10:52750736-52750786	HRPEpiC	eye:	n/a
28	chr10:52750754-52750804	MCF-7	breast:	n/a
29	chr10:52750743-52750793	AG10803	skin:	n/a
30	chr10:52751341-52751391	HepG2	liver:	n/a
31	chr10:52751764-52751814	HepG2	liver:	n/a
32	chr10:52752476-52752526	A549	lung:	n/a
33	chr10:52751764-52751814	NH-A	brain:	n/a
34	chr10:52751764-52751814	HCT-116	colon:	n/a
35	chr10:52754927-52754977	GM12892	blood:	n/a
36	chr10:52750930-52750980	Jurkat	blood:	n/a
37	chr10:52750736-52750786	HIPEpiC	eye:	n/a
38	chr10:52750754-52750804	GM19239	blood:	n/a
39	chr10:52750296-52750346	AG04450	lung:	fetal
40	chr10:52750754-52750804	HUVEC	blood vessel:	n/a
41	chr10:52750930-52750980	HEK293	kidney:	embryo
42	chr10:52751341-52751391	Hepatocyte	liver:	n/a
43	chr10:52750296-52750346	SK-N-SH_RA	brain:	n/a
44	chr10:52761022-52761072	GM06990	blood:	n/a
45	chr10:52754927-52754977	LNCaP	prostate:	n/a
46	chr10:52750995-52751045	HCF	heart:	n/a
47	chr10:52750736-52750786	A549	lung:	n/a
48	chr10:52754927-52754977	HCT-116	colon:	n/a
49	chr10:52750754-52750804	GM12878	blood:	n/a
50	chr10:52751764-52751814	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:52759956..52762521-chr10:52764582..52767080,2	MCF-7	breast:
2	chr10:52675412..52677074-chr10:52691849..52693555,2	MCF-7	breast:
3	chr10:52703230..52705590-chr10:52707679..52709615,2	K562	blood:
4	chr10:52687836..52690549-chr10:52690761..52693731,2	MCF-7	breast:
5	chr10:52663290..52665949-chr10:52668028..52669647,2	K562	blood:
6	chr10:52770367..52771306-chr10:52807728..52808411,3	MCF-7	breast:
7	chr10:52675412..52677074-chr10:52691849..52693555,2	MCF-7	breast:
8	chr10:52663290..52665949-chr10:52668028..52669647,2	K562	blood:
9	chr10:52759956..52762521-chr10:52764582..52767080,2	MCF-7	breast:
10	chr10:52761120..52762328-chr10:52807357..52808643,3	MCF-7	breast:
11	chr10:52703181..52706079-chr10:52706925..52709529,2	K562	blood:
12	chr10:52692456..52694438-chr10:52716760..52719116,2	MCF-7	breast:
13	chr10:52728760..52730500-chr10:52731859..52733643,2	MCF-7	breast:
14	chr10:52728760..52730500-chr10:52731859..52733643,2	MCF-7	breast:
15	chr10:52770367..52771306-chr10:52807728..52808411,3	MCF-7	breast:
16	chr10:52703230..52705590-chr10:52707679..52709615,2	K562	blood:
17	chr10:52753176..52755262-chr10:52757762..52759407,2	MCF-7	breast:
18	chr10:52761120..52762328-chr10:52807357..52808643,3	MCF-7	breast:
19	chr10:52770484..52771339-chr10:52807377..52808118,3	MCF-7	breast:
20	chr10:52770812..52771759-chr10:53975194..53976139,3	K562	blood:
21	chr10:52692456..52694438-chr10:52716760..52719116,2	MCF-7	breast:
22	chr10:52805414..52807391-chr10:52810252..52811808,2	MCF-7	breast:
23	chr10:52805100..52807814-chr2:220435282..220438038,2	MCF-7	breast:
24	chr10:52733880..52736696-chr10:52738245..52740154,2	K562	blood:
25	chr10:52733880..52736696-chr10:52738245..52740154,2	K562	blood:
26	chr10:52703181..52706079-chr10:52706925..52709529,2	K562	blood:
27	chr10:52687836..52690549-chr10:52690761..52693731,2	MCF-7	breast:
28	chr10:52723112..52726088-chr10:52731594..52733932,2	MCF-7	breast:
29	chr10:52753176..52755262-chr10:52757762..52759407,2	MCF-7	breast:
30	chr10:52548462..52549320-chr10:52748178..52748838,2	MCF-7	breast:
31	chr10:52770484..52771339-chr10:52807377..52808118,3	MCF-7	breast:
32	chr10:52805414..52807391-chr10:52810252..52811808,2	MCF-7	breast:
33	chr10:52723114..52725819-chr10:52729870..52732057,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKG1-1	chr10:52724030-52724995	NONHSAT013403
2	lnc-A1CF-6	chr10:52722753-52723118	NONHSAT013402
3	lnc-PRKG1-1	chr10:52724030-52724980	ENSG00000261368.1
4	lnc-A1CF-8	chr10:52751352-52751481	NONHSAT013405
5	lnc-A1CF-8	chr10:52750729-52751213	NONHSAT013405
6	lnc-A1CF-8	chr10:52751298-52751481	NONHSAT013404
7	lnc-A1CF-8	chr10:52750729-52751213	NONHSAT013404

Variant related genes	Relation type
PRKG1	TF binding region
ENSG00000261368	TF binding region
CCDC58P2	TF binding region
PRKG1	CpG island
ENSG00000261368	CpG island
CCDC58P2	CpG island
ENSG00000123999	chromatin interactions
ENSG00000236944	chromatin interactions
ENSG00000124006	chromatin interactions
ENSG00000261368	chromatin interactions

Extended variants
information (count: 4383 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4383 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368863979	chr10:52668822-52668823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553161844	chr10:52668849-52668850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572956920	chr10:52668863-52668864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189147871	chr10:52668887-52668888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562619825	chr10:52668888-52668889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531668207	chr10:52668900-52668901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192188155	chr10:52668910-52668911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184458608	chr10:52668911-52668912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76153470	chr10:52668912-52668913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575404470	chr10:52668926-52668927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570966925	chr10:52668967-52668968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34927949	chr10:52668995-52668996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369605568	chr10:52669010-52669011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375030376	chr10:52669037-52669038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544615729	chr10:52669056-52669057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374424537	chr10:52669071-52669072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570236457	chr10:52669099-52669100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535758565	chr10:52669116-52669117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs59821686	chr10:52669158-52669159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555512139	chr10:52669212-52669213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7906631	chr10:52669260-52669261	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181453844	chr10:52669275-52669276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553576042	chr10:52669278-52669279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs578005707	chr10:52669293-52669294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576900526	chr10:52669359-52669360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545467936	chr10:52669431-52669432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562519185	chr10:52669432-52669433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576230061	chr10:52669434-52669435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186481351	chr10:52669493-52669494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140179130	chr10:52669499-52669500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560703548	chr10:52669500-52669501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149854575	chr10:52669520-52669521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115078112	chr10:52669542-52669543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189201225	chr10:52669552-52669553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533500670	chr10:52669583-52669584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368836501	chr10:52669585-52669586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549870547	chr10:52669608-52669609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570051538	chr10:52669619-52669620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529497112	chr10:52669739-52669740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549275305	chr10:52669744-52669745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560384515	chr10:52669783-52669784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533421959	chr10:52675218-52675219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558321863	chr10:52675274-52675275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374463780	chr10:52675326-52675327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114339272	chr10:52675431-52675432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570057483	chr10:52675439-52675440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538883504	chr10:52675450-52675451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369031206	chr10:52675468-52675469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557181429	chr10:52675488-52675489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555573826	chr10:52675514-52675515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52668800-52669800	Enhancers	Fetal Heart	heart
2	chr10:52675200-52677000	Weak transcription	Aorta	Aorta
3	chr10:52676800-52677800	Enhancers	NHEK	skin
4	chr10:52676800-52679000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr10:52676800-52679400	Enhancers	HMEC	breast
6	chr10:52677000-52677800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr10:52677000-52677800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr10:52677000-52677800	Enhancers	Aorta	Aorta
9	chr10:52677000-52678000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr10:52677000-52678000	Enhancers	NHLF	lung
11	chr10:52677000-52678200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:52677000-52679400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr10:52677200-52677800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr10:52677400-52677800	Enhancers	HSMMtube	muscle
15	chr10:52677800-52678800	Weak transcription	NHEK	skin
16	chr10:52677800-52679000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr10:52678000-52679000	Weak transcription	NHLF	lung
18	chr10:52678400-52679000	Enhancers	Left Ventricle	heart
19	chr10:52678800-52679000	Enhancers	NHEK	skin
20	chr10:52679000-52679200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr10:52679200-52679400	Enhancers	NHLF	lung
22	chr10:52682000-52682200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr10:52682800-52683600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:52683000-52683400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr10:52683000-52683400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr10:52683200-52687000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:52683400-52684000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr10:52683400-52686800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr10:52685200-52686200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr10:52686200-52686400	Enhancers	Esophagus	oesophagus
31	chr10:52686200-52686600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr10:52686600-52688000	Weak transcription	Esophagus	oesophagus
33	chr10:52686600-52689800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr10:52686800-52688400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr10:52686800-52688400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr10:52686800-52688400	Enhancers	NHEK	skin
37	chr10:52686800-52689800	Enhancers	HMEC	breast
38	chr10:52687000-52688200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr10:52687000-52689800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr10:52688000-52688400	Enhancers	Esophagus	oesophagus
41	chr10:52688000-52689800	Enhancers	Pancreas	Pancrea
42	chr10:52688200-52689200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr10:52688400-52689400	Weak transcription	NHEK	skin
44	chr10:52688400-52689600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr10:52689200-52689600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr10:52689200-52689600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr10:52689400-52689600	Enhancers	NHEK	skin
48	chr10:52689600-52689800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:52689600-52689800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr10:52689600-52691800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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