Variant report

Variant	nsv8600
Chromosome Location	chr10:5733691-5736727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:294)
CpG islands
(count:305)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5734791-5734856	K562	blood:	n/a	n/a
2	ARID3A	chr10:5734681-5735376	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5736177-5736325	HepG2	liver:	n/a	n/a
4	ATF2	chr10:5734707-5735139	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr10:5734574-5734857	K562	blood:	n/a	n/a
6	BACH1	chr10:5734414-5735236	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:5734963-5735160	K562	blood:	n/a	n/a
8	BCLAF1	chr10:5734444-5735296	GM12878	blood:	n/a	chr10:5734833-5734846 chr10:5735089-5735102
9	BCLAF1	chr10:5734492-5735055	GM12878	blood:	n/a	chr10:5734833-5734846
10	BHLHE40	chr10:5734654-5735364	K562	blood:	n/a	n/a
11	BHLHE40	chr10:5734605-5735204	HepG2	liver:	n/a	n/a
12	BHLHE40	chr10:5734348-5735479	GM12878	blood:	n/a	n/a
13	BRCA1	chr10:5734748-5734948	HepG2	liver:	n/a	n/a
14	CBX3	chr10:5734564-5735338	K562	blood:	n/a	n/a
15	CCNT2	chr10:5734447-5735080	K562	blood:	n/a	n/a
16	CEBPB	chr10:5734613-5735436	HepG2	liver:	n/a	chr10:5735261-5735274
17	CEBPB	chr10:5734989-5735469	HepG2	liver:	n/a	chr10:5735261-5735274
18	CEBPB	chr10:5734821-5735321	H1-hESC	embryonic stem cell:	n/a	chr10:5735261-5735274
19	CEBPB	chr10:5735045-5735375	K562	blood:	n/a	chr10:5735261-5735274
20	CEBPD	chr10:5734581-5735282	HepG2	liver:	n/a	n/a
21	CHD1	chr10:5734278-5735602	GM12878	blood:	n/a	n/a
22	CHD2	chr10:5734681-5735071	K562	blood:	n/a	n/a
23	CHD2	chr10:5734493-5735185	GM12878	blood:	n/a	n/a
24	CHD2	chr10:5734434-5735038	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr10:5734398-5735170	HepG2	liver:	n/a	n/a
26	CREB1	chr10:5734173-5735056	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr10:5734368-5734606	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr10:5734334-5734920	A549	lung:	n/a	n/a
29	CREB1	chr10:5734446-5735187	K562	blood:	n/a	n/a
30	CREB1	chr10:5734264-5735175	GM12878	blood:	n/a	n/a
31	CTBP2	chr10:5734410-5735178	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr10:5735120-5735270	MCF-7	breast:	n/a	n/a
33	CTCF	chr10:5734660-5734810	GM12873	blood:	n/a	n/a
34	CTCF	chr10:5734782-5734844	GM12878	blood:	n/a	n/a
35	CTCF	chr10:5734816-5735190	K562	blood:	n/a	n/a
36	CTCF	chr10:5734680-5734830	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr10:5734680-5734830	GM12871	blood:	n/a	n/a
38	CTCF	chr10:5734960-5735110	GM12870	blood:	n/a	n/a
39	CTCF	chr10:5734660-5734810	GM12870	blood:	n/a	n/a
40	CTCF	chr10:5734380-5734530	HAc	cerebellar:	n/a	n/a
41	CUX1	chr10:5736287-5736565	K562	blood:	n/a	n/a
42	CUX1	chr10:5735210-5735331	K562	blood:	n/a	n/a
43	CUX1	chr10:5736336-5736868	GM12878	blood:	n/a	n/a
44	E2F4	chr10:5734558-5734947	GM12878	blood:	n/a	n/a
45	E2F4	chr10:5734667-5734904	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F6	chr10:5734396-5734552	K562	blood:	n/a	n/a
47	E2F6	chr10:5734576-5735025	K562	blood:	n/a	chr10:5734812-5734823
48	E2F6	chr10:5734397-5735120	K562	blood:	n/a	chr10:5734812-5734823
49	E2F6	chr10:5734518-5735244	A549	lung:	n/a	chr10:5734812-5734823
50	E2F6	chr10:5734672-5735071	K562	blood:	n/a	chr10:5734812-5734823

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5734985-5735035	HEK293	kidney:	embryo
2	chr10:5734716-5734766	H1-hESC	embryonic stem cell:	embryo
3	chr10:5735349-5735399	AoSMC	blood vessel:	n/a
4	chr10:5734716-5734766	Hela-S3	cervix:	n/a
5	chr10:5734985-5735035	HUVEC	blood vessel:	n/a
6	chr10:5735349-5735399	RPTEC	kidney:	n/a
7	chr10:5735349-5735399	MCF10A-Er-Src	breast:	n/a
8	chr10:5734571-5734621	HRE	kidney:	n/a
9	chr10:5734716-5734766	AG09309	skin:	n/a
10	chr10:5735135-5735185	SKMC	muscle:	n/a
11	chr10:5734716-5734766	Hepatocyte	liver:	n/a
12	chr10:5735135-5735185	MCF-7	breast:	n/a
13	chr10:5735135-5735185	SK-N-MC	brain:	n/a
14	chr10:5734985-5735035	NHBE	bronchial:	n/a
15	chr10:5735135-5735185	LNCaP	prostate:	n/a
16	chr10:5735349-5735399	SAEC	small airway:	n/a
17	chr10:5734571-5734621	HRPEpiC	eye:	n/a
18	chr10:5734571-5734621	SK-N-SH_RA	brain:	n/a
19	chr10:5735349-5735399	GM12878	blood:	n/a
20	chr10:5734571-5734621	RPTEC	kidney:	n/a
21	chr10:5734985-5735035	LNCaP	prostate:	n/a
22	chr10:5734716-5734766	PANC-1	pancreas:	n/a
23	chr10:5734716-5734766	HRPEpiC	eye:	n/a
24	chr10:5735135-5735185	GM12891	blood:	n/a
25	chr10:5734985-5735035	PrEC	prostate:	n/a
26	chr10:5735135-5735185	HCT-116	colon:	n/a
27	chr10:5735349-5735399	NHDF-neo	bronchial:	n/a
28	chr10:5734985-5735035	ovcar-3	ovarian:	n/a
29	chr10:5735349-5735399	LNCaP	prostate:	n/a
30	chr10:5735349-5735399	PFSK-1	brain:	n/a
31	chr10:5734571-5734621	HRCEpiC	kidney:	n/a
32	chr10:5734716-5734766	HepG2	liver:	n/a
33	chr10:5734571-5734621	A549	lung:	n/a
34	chr10:5734985-5735035	NHDF-neo	bronchial:	n/a
35	chr10:5735135-5735185	GM06990	blood:	n/a
36	chr10:5735135-5735185	T-47D	breast:	n/a
37	chr10:5734985-5735035	GM12878	blood:	n/a
38	chr10:5734571-5734621	AoSMC	blood vessel:	n/a
39	chr10:5734571-5734621	AG09319	gingival:	n/a
40	chr10:5734571-5734621	GM12891	blood:	n/a
41	chr10:5735135-5735185	NH-A	brain:	n/a
42	chr10:5734571-5734621	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:5734571-5734621	ECC-1	luminal epithelium:	n/a
44	chr10:5735349-5735399	H1-hESC	embryonic stem cell:	embryo
45	chr10:5735349-5735399	AG04449	skin:	fetal
46	chr10:5735135-5735185	NT2-D1	testis:	n/a
47	chr10:5734985-5735035	A549	lung:	n/a
48	chr10:5735349-5735399	HRE	kidney:	n/a
49	chr10:5734716-5734766	HEK293	kidney:	embryo
50	chr10:5734716-5734766	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:5734758..5736346-chr10:5739333..5741720,2	MCF-7	breast:
2	chr10:5487726..5489985-chr10:5734513..5736734,3	K562	blood:
3	chr10:5702075..5704019-chr10:5735223..5736822,2	MCF-7	breast:
4	chr10:5732056..5734929-chr10:5855542..5857938,2	K562	blood:
5	chr10:5733731..5736743-chr10:5750015..5755601,4	MCF-7	breast:
6	chr10:5706961..5708705-chr10:5733482..5736246,2	K562	blood:
7	chr10:5487726..5489985-chr10:5734513..5736734,2	K562	blood:
8	chr10:5722939..5725566-chr10:5730999..5734048,3	K562	blood:
9	chr10:5733787..5736575-chr10:5751182..5753712,2	MCF-7	breast:
10	chr10:5731846..5734735-chr10:5789579..5792999,3	K562	blood:
11	chr10:5735790..5738712-chr10:5931841..5933412,2	MCF-7	breast:
12	chr10:5734808..5736462-chr10:5936256..5938867,2	K562	blood:
13	chr10:5726775..5729176-chr10:5734287..5736106,2	MCF-7	breast:
14	chr10:5724274..5728540-chr10:5734829..5741563,8	MCF-7	breast:
15	chr10:5732626..5734143-chr10:5754788..5756828,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALML3-1	chr10:5734779-5734881	NONHSAT011176

No data

Variant related genes	Relation type
FAM208B	TF binding region
FAM208B	CpG island
ENSG00000057608	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000272764	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000108021	chromatin interactions
ENSG00000226647	chromatin interactions
ENSG00000196372	chromatin interactions
ENSG00000134461	chromatin interactions

Extended variants
information (count: 128 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:128 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554901371	chr10:5733750-5733751	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs538862856	chr10:5733802-5733803	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs79764755	chr10:5733816-5733817	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs537925495	chr10:5733912-5733913	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs181116850	chr10:5733928-5733929	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs578116629	chr10:5733952-5733953	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs114294414	chr10:5734021-5734022	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs77719694	chr10:5734041-5734042	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs139475750	chr10:5734053-5734054	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs186805268	chr10:5734082-5734083	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs3047334	chr10:5734112-5734113	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs386370558	chr10:5734113-5734114	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs386370559	chr10:5734124-5734125	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs71388464	chr10:5734127-5734128	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs377752264	chr10:5734128-5734129	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs369589012	chr10:5734129-5734130	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs537682151	chr10:5734161-5734162	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs2892072	chr10:5734220-5734221	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs531738443	chr10:5734283-5734284	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs190121291	chr10:5734292-5734293	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs562581930	chr10:5734320-5734321	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs533147211	chr10:5734346-5734347	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs9423936	chr10:5734358-5734359	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs566437441	chr10:5734413-5734414	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs527554958	chr10:5734424-5734425	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs548598242	chr10:5734430-5734431	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs116303287	chr10:5734456-5734457	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs538753604	chr10:5734491-5734492	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs556224243	chr10:5734549-5734550	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs151006432	chr10:5734559-5734560	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs539232432	chr10:5734573-5734574	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs554374940	chr10:5734583-5734584	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs572797077	chr10:5734601-5734602	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs575225942	chr10:5734612-5734613	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs372395165	chr10:5734613-5734614	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs543318842	chr10:5734648-5734649	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs555034433	chr10:5734673-5734674	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs576373562	chr10:5734682-5734683	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs560084676	chr10:5734687-5734688	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs543598922	chr10:5734743-5734744	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs74483336	chr10:5734744-5734745	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs532459044	chr10:5734793-5734794	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
43	rs117638247	chr10:5734802-5734803	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs559894703	chr10:5734805-5734806	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
45	rs527616463	chr10:5734825-5734826	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
46	rs548857696	chr10:5734828-5734829	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
47	rs11259632	chr10:5734863-5734864	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
48	rs2386621	chr10:5734869-5734870	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs549473611	chr10:5734907-5734908	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs182270575	chr10:5734928-5734929	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Melanoma	17363583	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
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5727800-5733800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:5728000-5734400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:5728200-5733800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr10:5728200-5733800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr10:5728200-5733800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:5728200-5733800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr10:5728200-5733800	Weak transcription	Fetal Muscle Leg	muscle
8	chr10:5728200-5733800	Weak transcription	Gastric	stomach
9	chr10:5728200-5733800	Weak transcription	Lung	lung
10	chr10:5728200-5734000	Weak transcription	Esophagus	oesophagus
11	chr10:5728200-5734200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:5728200-5734400	Weak transcription	Aorta	Aorta
13	chr10:5728400-5734400	Weak transcription	HSMM	muscle
14	chr10:5728600-5733800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr10:5728600-5733800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr10:5728600-5733800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr10:5728600-5733800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr10:5728600-5733800	Weak transcription	Brain Germinal Matrix	brain
19	chr10:5728600-5733800	Weak transcription	Brain Substantia Nigra	brain
20	chr10:5728600-5733800	Weak transcription	Fetal Thymus	thymus
21	chr10:5728600-5733800	Weak transcription	Psoas Muscle	Psoas
22	chr10:5728600-5734000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr10:5728600-5734000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr10:5728600-5734200	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr10:5728600-5734200	Weak transcription	Brain Hippocampus Middle	brain
26	chr10:5728600-5734200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr10:5728600-5734200	Weak transcription	Right Ventricle	heart
28	chr10:5728600-5734200	Weak transcription	Stomach Smooth Muscle	stomach
29	chr10:5728600-5734200	Weak transcription	Thymus	Thymus
30	chr10:5728800-5733800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr10:5728800-5733800	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr10:5728800-5733800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr10:5728800-5733800	Weak transcription	Fetal Lung	lung
34	chr10:5728800-5733800	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr10:5728800-5733800	Weak transcription	HUVEC	blood vessel
36	chr10:5728800-5733800	Weak transcription	Osteobl	bone
37	chr10:5728800-5734000	Weak transcription	Adipose Nuclei	Adipose
38	chr10:5728800-5734000	Weak transcription	Brain Anterior Caudate	brain
39	chr10:5728800-5734200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr10:5728800-5734200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr10:5728800-5734200	Weak transcription	Fetal Kidney	kidney
42	chr10:5728800-5734200	Weak transcription	NHLF	lung
43	chr10:5728800-5746800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr10:5729000-5734000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:5729000-5734000	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr10:5729200-5733800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr10:5729200-5733800	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr10:5729200-5733800	Weak transcription	Duodenum Mucosa	Duodenum
49	chr10:5729400-5733800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr10:5729400-5733800	Weak transcription	Rectal Smooth Muscle	rectum

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