Variant report

Variant	nsv515534
Chromosome Location	chr15:52998262-53025692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 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	chr15:53001404-53001641	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:53025336-53025762	HepG2	liver:	n/a	n/a
3	BHLHE40	chr15:53022411-53022779	K562	blood:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
4	BHLHE40	chr15:53022151-53022783	GM12878	blood:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
5	BHLHE40	chr15:53022405-53022675	HepG2	liver:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
6	BRCA1	chr15:53003829-53003910	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr15:53021054-53021493	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr15:53025415-53025697	HepG2	liver:	n/a	chr15:53025567-53025578
9	CEBPB	chr15:53025384-53025753	HepG2	liver:	n/a	chr15:53025567-53025578
10	CEBPB	chr15:53012468-53012470	A549	lung:	n/a	n/a
11	CEBPB	chr15:53007378-53007639	HepG2	liver:	n/a	n/a
12	CEBPB	chr15:53015920-53016153	A549	lung:	n/a	n/a
13	CEBPB	chr15:53001315-53001704	HepG2	liver:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
14	CEBPB	chr15:53021130-53021481	IMR90	lung:	n/a	n/a
15	CEBPB	chr15:53021098-53021506	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr15:53025408-53025729	K562	blood:	n/a	chr15:53025567-53025578
17	CEBPB	chr15:53025372-53025801	HepG2	liver:	n/a	chr15:53025567-53025578
18	CEBPB	chr15:53015982-53016146	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr15:53012270-53012669	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr15:53001361-53001671	IMR90	lung:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
21	CEBPB	chr15:53025447-53025711	HepG2	liver:	n/a	chr15:53025567-53025578
22	CEBPB	chr15:53001375-53001589	HepG2	liver:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
23	CEBPB	chr15:53001333-53001688	Hela-S3	cervix:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
24	CEBPB	chr15:53025362-53025763	Hela-S3	cervix:	n/a	chr15:53025567-53025578
25	CEBPD	chr15:53025449-53025682	HepG2	liver:	n/a	chr15:53025568-53025579
26	CTCF	chr15:53022540-53022690	GM12868	blood:	n/a	n/a
27	CTCF	chr15:53009579-53009640	GM20000	blood:	n/a	n/a
28	CTCF	chr15:53022488-53022650	MCF-7	breast:	n/a	n/a
29	CTCF	chr15:53022520-53022670	SAEC	small airway:	n/a	n/a
30	CTCF	chr15:53022515-53022616	MCF-7	breast:	n/a	n/a
31	CTCF	chr15:53022560-53022710	GM12873	blood:	n/a	n/a
32	CTCF	chr15:53022480-53022630	AG04449	skin:	n/a	n/a
33	CTCF	chr15:53002420-53002570	GM12873	blood:	n/a	n/a
34	CTCF	chr15:53022504-53022647	GM13977	blood:	n/a	n/a
35	CTCF	chr15:53022395-53022759	GM12878	blood:	n/a	n/a
36	CTCF	chr15:53022460-53022610	GM12872	blood:	n/a	n/a
37	CTCF	chr15:53022500-53022650	GM06990	blood:	n/a	n/a
38	CTCF	chr15:53022540-53022690	GM12864	blood:	n/a	n/a
39	CTCF	chr15:53022499-53022589	GM19239	blood:	n/a	n/a
40	CTCF	chr15:53022400-53022550	GM12873	blood:	n/a	n/a
41	CTCF	chr15:53022440-53022590	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:53022500-53022650	GM12864	blood:	n/a	n/a
43	CTCF	chr15:53022540-53022690	GM06990	blood:	n/a	n/a
44	CTCF	chr15:53022598-53022675	GM13976	blood:	n/a	n/a
45	CTCF	chr15:53022494-53022682	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr15:53004320-53004470	GM12865	blood:	n/a	n/a
47	CTCF	chr15:53010060-53010210	GM12872	blood:	n/a	n/a
48	CTCF	chr15:53022480-53022630	GM12875	blood:	n/a	n/a
49	CTCF	chr15:53022514-53022630	Lung_OC	lung:	n/a	n/a
50	CTCF	chr15:53022480-53022630	GM12864	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53001117-53001167	Caco-2	colon:	n/a
2	chr15:53001117-53001167	HNPCEpiC	eye:	n/a
3	chr15:53001117-53001167	AG09309	skin:	n/a
4	chr15:53001117-53001167	PANC-1	pancreas:	n/a
5	chr15:53001117-53001167	SK-N-MC	brain:	n/a
6	chr15:53001117-53001167	HepG2	liver:	n/a
7	chr15:53001117-53001167	AG09319	gingival:	n/a
8	chr15:53001117-53001167	NH-A	brain:	n/a
9	chr15:53001117-53001167	GM06990	blood:	n/a
10	chr15:53001117-53001167	HRE	kidney:	n/a
11	chr15:53001117-53001167	NB4	blood:	n/a
12	chr15:53001117-53001167	Hepatocyte	liver:	n/a
13	chr15:53001117-53001167	H1-hESC	embryonic stem cell:	embryo
14	chr15:53001117-53001167	NHDF-neo	bronchial:	n/a
15	chr15:53001117-53001167	HCT-116	colon:	n/a
16	chr15:53001117-53001167	BJ	skin:	n/a
17	chr15:53001117-53001167	SAEC	small airway:	n/a
18	chr15:53001117-53001167	IMR90	lung:	fetal
19	chr15:53001117-53001167	CMK	blood:	n/a
20	chr15:53001117-53001167	MCF-7	breast:	n/a
21	chr15:53001117-53001167	AG04450	lung:	fetal
22	chr15:53001117-53001167	HCPEpiC	choroid plexus:	n/a
23	chr15:53001117-53001167	HRPEpiC	eye:	n/a
24	chr15:53001117-53001167	GM12878	blood:	n/a
25	chr15:53001117-53001167	K562	blood:	n/a
26	chr15:53001117-53001167	GM12892	blood:	n/a
27	chr15:53001117-53001167	HAEpiC	amniotic membrane:	n/a
28	chr15:53001117-53001167	HL-60	blood:	n/a
29	chr15:53001117-53001167	U87	brain:	n/a
30	chr15:53001117-53001167	PrEC	prostate:	n/a
31	chr15:53001117-53001167	HMEC	breast:	n/a
32	chr15:53001117-53001167	AoSMC	blood vessel:	n/a
33	chr15:53001117-53001167	HRCEpiC	kidney:	n/a
34	chr15:53001117-53001167	HEK293	kidney:	embryo
35	chr15:53001117-53001167	A549	lung:	n/a
36	chr15:53001117-53001167	AG04449	skin:	fetal
37	chr15:53001117-53001167	LNCaP	prostate:	n/a
38	chr15:53001117-53001167	RPTEC	kidney:	n/a
39	chr15:53001117-53001167	ovcar-3	ovarian:	n/a
40	chr15:53001117-53001167	HPAEpiC	pulmonary alveolar:	n/a
41	chr15:53001117-53001167	T-47D	breast:	n/a
42	chr15:53001117-53001167	Hela-S3	cervix:	n/a
43	chr15:53001117-53001167	HUVEC	blood vessel:	n/a
44	chr15:53001117-53001167	Jurkat	blood:	n/a
45	chr15:53001117-53001167	NT2-D1	testis:	n/a
46	chr15:53001117-53001167	HCF	heart:	n/a
47	chr15:53001117-53001167	SK-N-SH_RA	brain:	n/a
48	chr15:53001117-53001167	AG10803	skin:	n/a
49	chr15:53001117-53001167	BE2_C	brain:	n/a
50	chr15:53001117-53001167	ProgFib	skin:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:53006205..53008987-chr15:53009449..53012016,3	MCF-7	breast:
2	chr15:53002359..53006038-chr15:53007315..53009805,4	K562	blood:
3	chr15:52860064..52861646-chr15:53023947..53025473,2	MCF-7	breast:
4	chr15:52844953..52847640-chr15:53010163..53013098,2	MCF-7	breast:
5	chr15:52969966..52973260-chr15:53007866..53011792,4	MCF-7	breast:
6	chr15:52969340..52972976-chr15:53024542..53030044,12	MCF-7	breast:
7	chr15:52628155..52629955-chr15:53015410..53018106,2	MCF-7	breast:
8	chr15:52979304..52981911-chr15:53011644..53013861,2	MCF-7	breast:
9	chr15:53001798..53003547-chr15:53015558..53017626,2	MCF-7	breast:
10	chr15:52981751..52983702-chr15:52997065..52999540,2	MCF-7	breast:
11	chr15:52968697..52973342-chr15:53018163..53028590,24	MCF-7	breast:
12	chr15:52849763..52852458-chr15:53021230..53022756,2	MCF-7	breast:
13	chr15:52991504..52994033-chr15:53002922..53004759,2	MCF-7	breast:
14	chr15:53020023..53021825-chr15:53025584..53028001,2	MCF-7	breast:
15	chr15:52987035..52988935-chr15:53020479..53022010,2	MCF-7	breast:
16	chr15:52978223..52981172-chr15:53005234..53007666,2	MCF-7	breast:
17	chr15:52991521..52993410-chr15:52996311..52999236,2	MCF-7	breast:
18	chr15:52820586..52822979-chr15:53024504..53027126,2	MCF-7	breast:
19	chr15:52998097..53002621-chr15:53002876..53006188,5	K562	blood:
20	chr15:52965949..52968646-chr15:53025332..53028243,3	MCF-7	breast:
21	chr15:52888619..52891451-chr15:53020250..53023070,2	MCF-7	breast:
22	chr15:53002359..53006038-chr15:53007315..53009805,4	K562	blood:
23	chr15:52970778..52973073-chr15:53012277..53014291,2	MCF-7	breast:
24	chr15:52967780..52973455-chr15:53015921..53024493,22	MCF-7	breast:
25	chr15:53020211..53022742-chr15:53022811..53024880,2	MCF-7	breast:
26	chr15:53022444..53024405-chr15:53025609..53027744,2	MCF-7	breast:
27	chr15:52968259..52973250-chr15:52997483..53005703,18	MCF-7	breast:
28	chr15:52986948..52989428-chr15:52996280..52998700,2	MCF-7	breast:
29	chr15:52587244..52588799-chr15:53018696..53021344,2	MCF-7	breast:
30	chr15:53020023..53021825-chr15:53025584..53028001,2	MCF-7	breast:
31	chr15:52970614..52972574-chr15:53011299..53014236,2	MCF-7	breast:
32	chr15:52942373..52946105-chr15:53022429..53026141,4	MCF-7	breast:
33	chr15:53022444..53024405-chr15:53025609..53027744,2	MCF-7	breast:
34	chr15:53008460..53014321-chr15:53016290..53019599,5	MCF-7	breast:
35	chr15:53008460..53014321-chr15:53016290..53019599,5	MCF-7	breast:
36	chr15:53014375..53016603-chr15:53017308..53019885,2	MCF-7	breast:
37	chr15:53017085..53018702-chr15:53021319..53022831,2	MCF-7	breast:
38	chr15:52970779..52973636-chr15:53016610..53018142,2	MCF-7	breast:
39	chr15:53020211..53022742-chr15:53022811..53024880,2	MCF-7	breast:
40	chr15:53014375..53016603-chr15:53017308..53019885,2	MCF-7	breast:
41	chr15:52966586..52968208-chr15:53018199..53019999,2	MCF-7	breast:
42	chr15:52973784..52977367-chr15:53024530..53026901,4	MCF-7	breast:
43	chr15:53017085..53018702-chr15:53021319..53022831,2	MCF-7	breast:
44	chr15:52967401..52973659-chr15:53000765..53004676,11	MCF-7	breast:
45	chr15:52623345..52624286-chr15:53022394..53023020,2	MCF-7	breast:
46	chr15:53006205..53008987-chr15:53009449..53012016,3	MCF-7	breast:

No data

Variant related genes	Relation type
FAM214A	TF binding region
FAM214A	CpG island
ENSG00000047346	chromatin interactions
ENSG00000128989	chromatin interactions
ENSG00000197535	chromatin interactions
ENSG00000128833	chromatin interactions

Extended variants
information (count: 1062 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1062 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6493573	chr15:52998262-52998263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs8031716	chr15:52998283-52998284	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs563819989	chr15:52998312-52998313	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575843382	chr15:52998357-52998358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546035876	chr15:52998364-52998365	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564250261	chr15:52998369-52998370	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370309517	chr15:52998408-52998409	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185470124	chr15:52998431-52998432	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528532232	chr15:52998451-52998452	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546612898	chr15:52998485-52998486	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs561776083	chr15:52998487-52998488	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189899395	chr15:52998517-52998518	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs72740221	chr15:52998555-52998556	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182030558	chr15:52998576-52998577	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569052794	chr15:52998604-52998605	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs145355123	chr15:52998611-52998612	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34384382	chr15:52998653-52998654	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147209907	chr15:52998661-52998662	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186476607	chr15:52998664-52998665	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533841804	chr15:52998679-52998680	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555478103	chr15:52998722-52998723	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573721724	chr15:52998774-52998775	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs73409649	chr15:52998817-52998818	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs9806571	chr15:52998842-52998843	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs575810237	chr15:52998852-52998853	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546393795	chr15:52998862-52998863	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78868946	chr15:52998935-52998936	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573080737	chr15:52998947-52998948	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189344627	chr15:52998981-52998982	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs59874444	chr15:52999066-52999067	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9806580	chr15:52999069-52999070	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs151204151	chr15:52999070-52999071	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs180884871	chr15:52999073-52999074	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs139087296	chr15:52999103-52999104	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149917577	chr15:52999136-52999137	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185785413	chr15:52999186-52999187	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs191592053	chr15:52999211-52999212	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs527465043	chr15:52999230-52999231	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs35008534	chr15:52999233-52999234	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114967168	chr15:52999238-52999239	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567324604	chr15:52999370-52999371	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537860061	chr15:52999389-52999390	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs114729538	chr15:52999569-52999570	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs76257791	chr15:52999601-52999602	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539772900	chr15:52999644-52999645	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534476422	chr15:52999680-52999681	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs140761494	chr15:52999792-52999793	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527873995	chr15:52999946-52999947	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs144613077	chr15:52999964-52999965	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555444000	chr15:52999980-52999981	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52995000-52999600	Weak transcription	Primary B cells from peripheral blood	blood
2	chr15:52995800-53001600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr15:52997800-52998800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr15:52998200-52998400	Enhancers	Liver	Liver
5	chr15:52998200-52998800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr15:52998200-52998800	Enhancers	NHEK	skin
7	chr15:52998200-52999200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr15:52998200-52999400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr15:52998400-52998800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr15:52998400-52999000	Flanking Active TSS	Liver	Liver
11	chr15:52998400-52999000	Enhancers	HSMM	muscle
12	chr15:52998800-53000800	Enhancers	Primary B cells from cord blood	blood
13	chr15:52998800-53001000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr15:52998800-53001200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:52998800-53001600	Weak transcription	NHEK	skin
16	chr15:52998800-53002200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:52999000-52999200	Active TSS	Liver	Liver
18	chr15:52999200-52999400	Flanking Active TSS	Liver	Liver
19	chr15:52999400-52999800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:52999400-53000200	Active TSS	Liver	Liver
21	chr15:52999600-53001000	Enhancers	Primary B cells from peripheral blood	blood
22	chr15:52999800-53001200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr15:53000200-53000800	Flanking Active TSS	Liver	Liver
24	chr15:53000400-53000600	Enhancers	Adipose Nuclei	Adipose
25	chr15:53000400-53001200	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr15:53000400-53001200	Enhancers	HepG2	liver
27	chr15:53000600-53001000	Enhancers	Fetal Intestine Large	intestine
28	chr15:53000800-53001000	Active TSS	Liver	Liver
29	chr15:53000800-53001800	Weak transcription	Adipose Nuclei	Adipose
30	chr15:53000800-53002000	Flanking Active TSS	Primary B cells from cord blood	blood
31	chr15:53001000-53001200	Flanking Active TSS	Liver	Liver
32	chr15:53001000-53001200	Enhancers	Duodenum Mucosa	Duodenum
33	chr15:53001000-53001200	Flanking Active TSS	Fetal Intestine Large	intestine
34	chr15:53001000-53001200	Enhancers	Fetal Intestine Small	intestine
35	chr15:53001000-53001400	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr15:53001000-53001600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr15:53001000-53001600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr15:53001000-53001800	Enhancers	GM12878-XiMat	blood
39	chr15:53001000-53002200	Flanking Active TSS	Primary B cells from peripheral blood	blood
40	chr15:53001200-53001600	Active TSS	Liver	Liver
41	chr15:53001200-53001800	Flanking Active TSS	Duodenum Mucosa	Duodenum
42	chr15:53001200-53002000	Active TSS	Fetal Intestine Large	intestine
43	chr15:53001200-53002000	Active TSS	Fetal Intestine Small	intestine
44	chr15:53001200-53002400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr15:53001200-53002600	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr15:53001200-53002800	Flanking Active TSS	HepG2	liver
47	chr15:53001400-53001600	Enhancers	H1 Cell Line	embryonic stem cell
48	chr15:53001400-53001600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr15:53001400-53001600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr15:53001400-53001800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell

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