Variant report

Variant	nsv1048186
Chromosome Location	chr10:58343941-58475146
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	ATF2	chr10:58393677-58394392	GM12878	blood:	n/a	n/a
2	ATF2	chr10:58412944-58413514	GM12878	blood:	n/a	n/a
3	ATF2	chr10:58393859-58394401	GM12878	blood:	n/a	n/a
4	ATF2	chr10:58413072-58413421	GM12878	blood:	n/a	n/a
5	BATF	chr10:58392302-58392666	GM12878	blood:	n/a	chr10:58392517-58392528
6	BATF	chr10:58356028-58356235	GM12878	blood:	n/a	chr10:58356125-58356136
7	BATF	chr10:58413137-58413422	GM12878	blood:	n/a	n/a
8	BATF	chr10:58393849-58394184	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:58393836-58394267	GM12878	blood:	n/a	n/a
10	BCL11A	chr10:58393892-58394170	GM12878	blood:	n/a	n/a
11	BCLAF1	chr10:58393692-58394349	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:58393840-58394442	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:58422586-58422736	GM12878	blood:	n/a	n/a
14	CEBPB	chr10:58427632-58427869	HepG2	liver:	n/a	chr10:58427746-58427757
15	CEBPB	chr10:58389499-58389707	A549	lung:	n/a	chr10:58389639-58389650
16	CEBPB	chr10:58427588-58427860	IMR90	lung:	n/a	chr10:58427746-58427757
17	CEBPB	chr10:58458311-58458645	IMR90	lung:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
18	CEBPB	chr10:58454437-58454792	IMR90	lung:	n/a	n/a
19	CEBPB	chr10:58454369-58454740	A549	lung:	n/a	n/a
20	CEBPB	chr10:58458325-58458631	K562	blood:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
21	CEBPB	chr10:58473662-58473927	IMR90	lung:	n/a	chr10:58473775-58473786 chr10:58473775-58473788
22	CEBPB	chr10:58475057-58475272	HepG2	liver:	n/a	chr10:58475139-58475150
23	CEBPB	chr10:58458348-58458586	Hela-S3	cervix:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
24	CEBPB	chr10:58454489-58454756	K562	blood:	n/a	n/a
25	CEBPB	chr10:58473719-58473849	K562	blood:	n/a	chr10:58473775-58473786 chr10:58473775-58473788
26	CEBPB	chr10:58458326-58458658	HepG2	liver:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
27	CEBPB	chr10:58364906-58365392	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr10:58458331-58458523	H1-hESC	embryonic stem cell:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
29	CEBPB	chr10:58458309-58458622	A549	lung:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
30	CEBPB	chr10:58397073-58397273	HepG2	liver:	n/a	chr10:58397224-58397235
31	CEBPB	chr10:58397140-58397340	A549	lung:	n/a	chr10:58397224-58397235
32	CEBPB	chr10:58389538-58389770	HepG2	liver:	n/a	chr10:58389639-58389650
33	CEBPB	chr10:58454387-58454781	HepG2	liver:	n/a	n/a
34	CEBPZ	chr10:58390422-58390450	HepG2	liver:	n/a	n/a
35	CHD1	chr10:58393767-58394099	GM12878	blood:	n/a	n/a
36	CHD2	chr10:58393742-58394425	GM12878	blood:	n/a	n/a
37	CHD2	chr10:58422681-58422872	GM12878	blood:	n/a	n/a
38	CTCF	chr10:58384006-58384077	GM19238	blood:	n/a	n/a
39	CTCF	chr10:58392280-58392430	GM12868	blood:	n/a	n/a
40	CTCF	chr10:58393979-58394119	GM12878	blood:	n/a	n/a
41	CTCF	chr10:58346260-58346410	HMEC	breast:	n/a	n/a
42	CTCF	chr10:58393998-58394096	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr10:58392360-58392510	GM12871	blood:	n/a	n/a
44	CTCF	chr10:58384040-58384072	GM12878	blood:	n/a	n/a
45	CTCF	chr10:58392420-58392570	GM12872	blood:	n/a	n/a
46	CTCF	chr10:58392300-58392450	GM12872	blood:	n/a	n/a
47	CTCF	chr10:58383980-58384130	GM12873	blood:	n/a	n/a
48	CTCF	chr10:58346180-58346330	NHEK	skin:	n/a	n/a
49	CTCF	chr10:58346220-58346370	HMEC	breast:	n/a	n/a
50	CTCF	chr10:58383980-58384130	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:58346379-58346429	HMEC	breast:	n/a
2	chr10:58346379-58346429	SKMC	muscle:	n/a
3	chr10:58346379-58346429	LNCaP	prostate:	n/a
4	chr10:58346379-58346429	Hepatocyte	liver:	n/a
5	chr10:58346379-58346429	MCF-7	breast:	n/a
6	chr10:58346379-58346429	CMK	blood:	n/a
7	chr10:58346379-58346429	BE2_C	brain:	n/a
8	chr10:58346379-58346429	Hela-S3	cervix:	n/a
9	chr10:58346379-58346429	HRE	kidney:	n/a
10	chr10:58346379-58346429	AG10803	skin:	n/a
11	chr10:58346379-58346429	AG09309	skin:	n/a
12	chr10:58346379-58346429	BJ	skin:	n/a
13	chr10:58346379-58346429	K562	blood:	n/a
14	chr10:58346379-58346429	RPTEC	kidney:	n/a
15	chr10:58346379-58346429	HRCEpiC	kidney:	n/a
16	chr10:58346379-58346429	ProgFib	skin:	n/a
17	chr10:58346379-58346429	AG04450	lung:	fetal
18	chr10:58346379-58346429	AoSMC	blood vessel:	n/a
19	chr10:58346379-58346429	HEEpiC	esophagus:	n/a
20	chr10:58346379-58346429	ovcar-3	ovarian:	n/a
21	chr10:58346379-58346429	HCPEpiC	choroid plexus:	n/a
22	chr10:58346379-58346429	HNPCEpiC	eye:	n/a
23	chr10:58346379-58346429	NHBE	bronchial:	n/a
24	chr10:58346379-58346429	SK-N-SH_RA	brain:	n/a
25	chr10:58346379-58346429	NB4	blood:	n/a
26	chr10:58346379-58346429	GM12878	blood:	n/a
27	chr10:58346379-58346429	PrEC	prostate:	n/a
28	chr10:58346379-58346429	SK-N-SH	brain:	n/a
29	chr10:58346379-58346429	IMR90	lung:	fetal
30	chr10:58346379-58346429	AG04449	skin:	fetal
31	chr10:58346379-58346429	Jurkat	blood:	n/a
32	chr10:58346379-58346429	SAEC	small airway:	n/a
33	chr10:58346379-58346429	GM12891	blood:	n/a
34	chr10:58346379-58346429	U87	brain:	n/a
35	chr10:58346379-58346429	HCF	heart:	n/a
36	chr10:58346379-58346429	PANC-1	pancreas:	n/a
37	chr10:58346379-58346429	HIPEpiC	eye:	n/a
38	chr10:58346379-58346429	A549	lung:	n/a
39	chr10:58346379-58346429	NHDF-neo	bronchial:	n/a
40	chr10:58346379-58346429	SK-N-MC	brain:	n/a
41	chr10:58346379-58346429	GM19239	blood:	n/a
42	chr10:58346379-58346429	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:58346379-58346429	NT2-D1	testis:	n/a
44	chr10:58346379-58346429	HepG2	liver:	n/a
45	chr10:58346379-58346429	HAEpiC	amniotic membrane:	n/a
46	chr10:58346379-58346429	ECC-1	luminal epithelium:	n/a
47	chr10:58346379-58346429	HEK293	kidney:	embryo
48	chr10:58346379-58346429	HUVEC	blood vessel:	n/a
49	chr10:58346379-58346429	PFSK-1	brain:	n/a
50	chr10:58346379-58346429	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:121484861..121485361-chr10:58418252..58418753,2	MCF-7	breast:
2	chr10:58412864..58414828-chr10:58418444..58421274,2	MCF-7	breast:
3	chr10:58360207..58362204-chr10:58364540..58367315,2	K562	blood:
4	chr10:58424658..58425526-chr10:58543096..58544051,4	MCF-7	breast:
5	chr10:58387072..58387735-chr9:109982409..109983123,2	MCF-7	breast:
6	chr10:58346871..58349130-chr10:58356428..58359069,2	MCF-7	breast:
7	chr10:58310627..58311484-chr10:58424524..58425160,3	MCF-7	breast:
8	chr10:58412864..58414828-chr10:58418444..58421274,2	MCF-7	breast:
9	chr10:58403682..58405609-chr10:58417401..58419090,2	K562	blood:
10	chr10:58458032..58460416-chr10:58460857..58463853,2	K562	blood:
11	chr10:58407921..58410026-chr12:33604212..33606934,2	MCF-7	breast:
12	chr10:58338696..58340505-chr10:58341566..58344213,2	K562	blood:
13	chr10:58458032..58460416-chr10:58460857..58463853,2	K562	blood:
14	chr10:58351002..58353905-chr5:28242920..28245430,2	MCF-7	breast:
15	chr10:58346871..58349130-chr10:58356428..58359069,2	MCF-7	breast:
16	chr10:58424561..58425526-chr10:58543081..58543976,4	MCF-7	breast:
17	chr10:58118622..58121394-chr10:58364437..58368069,3	K562	blood:
18	chr10:58360207..58362204-chr10:58364540..58367315,2	K562	blood:
19	chr10:58403682..58405609-chr10:58417401..58419090,2	K562	blood:

Variant related genes	Relation type
ENSG00000238707	TF binding region
ENSG00000238707	CpG island
ENSG00000122952	chromatin interactions

Extended variants
information (count: 1593 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369791971	chr10:58343996-58343997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112411209	chr10:58344000-58344001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527441217	chr10:58344004-58344005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373949528	chr10:58344058-58344059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567195825	chr10:58344062-58344063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11817010	chr10:58344080-58344081	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs549700154	chr10:58344132-58344133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs137923495	chr10:58344144-58344145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538707879	chr10:58344152-58344153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554188661	chr10:58344158-58344159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78268177	chr10:58344180-58344181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182819896	chr10:58344209-58344210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545688732	chr10:58344232-58344233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564179568	chr10:58344320-58344321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186384969	chr10:58344384-58344385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191242096	chr10:58344393-58344394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573503515	chr10:58344394-58344395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142191153	chr10:58344397-58344398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77936401	chr10:58344405-58344406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs61856107	chr10:58344463-58344464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542105957	chr10:58344465-58344466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562287144	chr10:58344468-58344469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560159501	chr10:58344470-58344471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140588347	chr10:58344473-58344474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542736287	chr10:58344558-58344559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34139010	chr10:58344563-58344564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560734786	chr10:58344589-58344590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150476619	chr10:58344604-58344605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34318789	chr10:58344614-58344615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549663417	chr10:58344656-58344657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74137807	chr10:58344664-58344665	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs532494088	chr10:58344677-58344678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570073778	chr10:58344712-58344713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369790138	chr10:58344754-58344755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148994807	chr10:58344761-58344762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536325222	chr10:58344783-58344784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539088826	chr10:58344789-58344790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs61856108	chr10:58344796-58344797	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs373420922	chr10:58344848-58344849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570253743	chr10:58344894-58344895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183533581	chr10:58344919-58344920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559247639	chr10:58344955-58344956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188532403	chr10:58344976-58344977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556040263	chr10:58345040-58345041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192650832	chr10:58345047-58345048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138345055	chr10:58345115-58345116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576316315	chr10:58345121-58345122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112121358	chr10:58345128-58345129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183171602	chr10:58345136-58345137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114172840	chr10:58345160-58345161	Weak transcription Enhancers	n/a	n/a	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
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
Obesity	21956041	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
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	20858243	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	17426248	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:58341800-58344000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:58341800-58344000	Enhancers	HMEC	breast
3	chr10:58341800-58344000	Enhancers	NHEK	skin
4	chr10:58341800-58344200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr10:58343200-58344000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr10:58343200-58345600	Enhancers	Fetal Heart	heart
7	chr10:58343600-58346200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:58343800-58344000	Enhancers	Left Ventricle	heart
9	chr10:58343800-58344000	Enhancers	Right Ventricle	heart
10	chr10:58344000-58346000	Weak transcription	HMEC	breast
11	chr10:58344000-58346200	Weak transcription	NHEK	skin
12	chr10:58344200-58345400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:58344800-58346000	Enhancers	Right Atrium	heart
14	chr10:58345400-58345600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr10:58345400-58346200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr10:58345400-58347200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr10:58345600-58346000	Flanking Active TSS	Fetal Heart	heart
18	chr10:58345600-58346200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr10:58345600-58346400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr10:58345600-58346400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr10:58345600-58346400	Enhancers	Left Ventricle	heart
22	chr10:58345600-58346400	Enhancers	Right Ventricle	heart
23	chr10:58345600-58346600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr10:58345600-58346600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr10:58345600-58346600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr10:58345600-58347200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr10:58345800-58346400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:58345800-58346400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr10:58345800-58346400	Enhancers	Esophagus	oesophagus
30	chr10:58345800-58346400	Enhancers	Fetal Brain Female	brain
31	chr10:58345800-58346600	Enhancers	Fetal Brain Male	brain
32	chr10:58345800-58346800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr10:58346000-58346200	Enhancers	Lung	lung
34	chr10:58346000-58346600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr10:58346000-58346800	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr10:58346000-58346800	Enhancers	Fetal Heart	heart
37	chr10:58346000-58346800	Enhancers	HMEC	breast
38	chr10:58346000-58347000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr10:58346000-58347400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr10:58346200-58346400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr10:58346200-58346600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr10:58346200-58346600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr10:58346200-58346600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr10:58346200-58346600	Enhancers	Fetal Stomach	stomach
45	chr10:58346200-58346600	Active TSS	NHEK	skin
46	chr10:58346400-58346600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr10:58346400-58347600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr10:58346400-58354000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr10:58346600-58346800	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr10:58347800-58348000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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