Variant report

Variant	nsv519319
Chromosome Location	chr15:99972661-99991506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:1344)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:99991175-99991347	K562	blood:	n/a	n/a
2	BACH1	chr15:99987944-99987962	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr15:99973687-99973691	GM12878	blood:	n/a	n/a
4	BRCA1	chr15:99975665-99975680	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr15:99991284-99991524	MCF-7	breast:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
6	CEBPB	chr15:99991175-99991573	ECC-1	luminal epithelium:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
7	CEBPB	chr15:99982704-99983088	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr15:99991224-99991516	K562	blood:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
9	CEBPB	chr15:99991138-99991628	ECC-1	luminal epithelium:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
10	CEBPB	chr15:99982646-99983055	IMR90	lung:	n/a	n/a
11	CEBPB	chr15:99991255-99991532	HepG2	liver:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
12	CEBPB	chr15:99991393-99991413	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr15:99991151-99991660	MCF-7	breast:	n/a	chr15:99991392-99991403 chr15:99991477-99991489 chr15:99991390-99991403 chr15:99991390-99991401
14	CHD2	chr15:99973694-99973933	GM12878	blood:	n/a	n/a
15	CHD2	chr15:99982693-99983140	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr15:99973825-99973857	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr15:99975690-99975908	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr15:99981080-99981230	BE2_C	brain:	n/a	n/a
19	CTCF	chr15:99973240-99973390	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr15:99975641-99975704	MCF-7	breast:	n/a	n/a
21	CTCF	chr15:99973400-99973550	GM12875	blood:	n/a	n/a
22	CTCF	chr15:99973798-99973839	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr15:99973674-99973785	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr15:99975580-99975730	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr15:99975720-99975870	MCF-7	breast:	n/a	n/a
26	CTCF	chr15:99978300-99978450	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr15:99975620-99975770	HMEC	breast:	n/a	n/a
28	CTCF	chr15:99975630-99975763	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr15:99973300-99973450	SAEC	small airway:	n/a	n/a
30	CTCF	chr15:99973300-99973450	GM12867	blood:	n/a	n/a
31	CTCF	chr15:99978397-99978442	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr15:99975560-99975710	SAEC	small airway:	n/a	n/a
33	CTCF	chr15:99973340-99973490	GM12873	blood:	n/a	n/a
34	CTCF	chr15:99975580-99975730	NHEK	skin:	n/a	n/a
35	CTCF	chr15:99973940-99974090	GM12871	blood:	n/a	chr15:99974036-99974049
36	CTCF	chr15:99973200-99973350	GM12867	blood:	n/a	chr15:99973237-99973250
37	CTCF	chr15:99975633-99975724	LNCaP	prostate:	n/a	n/a
38	CTCF	chr15:99975585-99975742	MCF-7	breast:	n/a	n/a
39	CTCF	chr15:99987020-99987170	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr15:99973360-99973510	GM12873	blood:	n/a	n/a
41	CTCF	chr15:99973787-99973793	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr15:99975666-99975752	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr15:99973260-99973410	GM12866	blood:	n/a	n/a
44	CTCF	chr15:99975620-99975770	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr15:99973300-99973450	HepG2	liver:	n/a	n/a
46	CTCF	chr15:99975600-99975750	Caco-2	colon:	n/a	n/a
47	CTCF	chr15:99975728-99975731	LNCaP	prostate:	n/a	n/a
48	CTCF	chr15:99973300-99973450	GM12870	blood:	n/a	n/a
49	CTCF	chr15:99973240-99973390	GM12864	blood:	n/a	n/a
50	CTCF	chr15:99975660-99975810	HMEC	breast:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:99974881-99974931	Hela-S3	cervix:	n/a
2	chr15:99975470-99975520	H1-hESC	embryonic stem cell:	embryo
3	chr15:99974881-99974931	Hela-S3	cervix:	n/a
4	chr15:99975470-99975520	H1-hESC	embryonic stem cell:	embryo
5	chr15:99975310-99975360	HepG2	liver:	n/a
6	chr15:99978986-99979036	HepG2	liver:	n/a
7	chr15:99979346-99979396	NT2-D1	testis:	n/a
8	chr15:99987871-99987921	HMEC	breast:	n/a
9	chr15:99979584-99979634	SK-N-SH_RA	brain:	n/a
10	chr15:99979527-99979577	NB4	blood:	n/a
11	chr15:99979013-99979063	Jurkat	blood:	n/a
12	chr15:99974369-99974419	Jurkat	blood:	n/a
13	chr15:99975470-99975520	ECC-1	luminal epithelium:	n/a
14	chr15:99987955-99988005	Caco-2	colon:	n/a
15	chr15:99975141-99975191	GM12878	blood:	n/a
16	chr15:99975334-99975384	U87	brain:	n/a
17	chr15:99974369-99974419	A549	lung:	n/a
18	chr15:99975334-99975384	HL-60	blood:	n/a
19	chr15:99979059-99979109	HUVEC	blood vessel:	n/a
20	chr15:99979346-99979396	GM06990	blood:	n/a
21	chr15:99974369-99974419	AG09319	gingival:	n/a
22	chr15:99987288-99987338	GM12878	blood:	n/a
23	chr15:99979346-99979396	HEEpiC	esophagus:	n/a
24	chr15:99974881-99974931	LNCaP	prostate:	n/a
25	chr15:99974881-99974931	GM12891	blood:	n/a
26	chr15:99979059-99979109	HAEpiC	amniotic membrane:	n/a
27	chr15:99982524-99982574	HepG2	liver:	n/a
28	chr15:99987871-99987921	AoSMC	blood vessel:	n/a
29	chr15:99975141-99975191	AG04449	skin:	fetal
30	chr15:99979346-99979396	ECC-1	luminal epithelium:	n/a
31	chr15:99987955-99988005	HCF	heart:	n/a
32	chr15:99974332-99974382	GM12878	blood:	n/a
33	chr15:99982524-99982574	AG04449	skin:	fetal
34	chr15:99975310-99975360	GM12892	blood:	n/a
35	chr15:99975310-99975360	BE2_C	brain:	n/a
36	chr15:99979346-99979396	PFSK-1	brain:	n/a
37	chr15:99987894-99987944	HCPEpiC	choroid plexus:	n/a
38	chr15:99974369-99974419	AG10803	skin:	n/a
39	chr15:99987871-99987921	GM06990	blood:	n/a
40	chr15:99974881-99974931	HEEpiC	esophagus:	n/a
41	chr15:99982524-99982574	LNCaP	prostate:	n/a
42	chr15:99975470-99975520	HAEpiC	amniotic membrane:	n/a
43	chr15:99979389-99979439	HRPEpiC	eye:	n/a
44	chr15:99987871-99987921	BJ	skin:	n/a
45	chr15:99978986-99979036	BE2_C	brain:	n/a
46	chr15:99979346-99979396	NHDF-neo	bronchial:	n/a
47	chr15:99975141-99975191	H1-hESC	embryonic stem cell:	embryo
48	chr15:99975334-99975384	NHDF-neo	bronchial:	n/a
49	chr15:99979059-99979109	HNPCEpiC	eye:	n/a
50	chr15:99987288-99987338	PrEC	prostate:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
2	chr15:99986076..99989977-chr15:99992374..99995201,3	K562	blood:
3	chr15:99981264..99984715-chr15:99985641..99987973,4	MCF-7	breast:
4	chr15:99976307..99978594-chr15:100018036..100019822,2	MCF-7	breast:
5	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
6	chr15:99977572..99979807-chr15:99980072..99982815,2	K562	blood:
7	chr15:99981781..99983657-chr15:100018041..100019744,2	MCF-7	breast:
8	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
9	chr15:99985824..99988050-chr15:99992595..99995524,2	MCF-7	breast:
10	chr15:99973224..99976448-chr15:99991050..99995157,5	MCF-7	breast:
11	chr15:99971316..99975999-chr15:100104042..100107403,7	MCF-7	breast:
12	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
13	chr15:99963793..99965594-chr15:99976352..99978718,2	K562	blood:
14	chr15:99977572..99979807-chr15:99980072..99982815,2	K562	blood:
15	chr15:99972394..99975109-chr15:99977541..99980166,2	MCF-7	breast:
16	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
17	chr15:99975615..99977769-chr15:99978276..99979849,2	MCF-7	breast:
18	chr15:99987398..99990235-chr15:100010575..100012559,2	MCF-7	breast:
19	chr15:99991338..99992840-chr15:100014340..100017006,2	MCF-7	breast:
20	chr15:99973224..99976448-chr15:99991050..99995157,5	MCF-7	breast:
21	chr15:99981264..99984715-chr15:99985641..99987973,4	MCF-7	breast:
22	chr15:99984466..99986504-chr15:100104174..100107057,2	K562	blood:
23	chr15:99979583..99981872-chr15:99983556..99985309,2	MCF-7	breast:
24	chr15:99975316..99977266-chr15:99981293..99982934,2	K562	blood:
25	chr15:99962979..99964880-chr15:99972892..99975204,2	MCF-7	breast:
26	chr15:99979674..99981771-chr15:99994725..99997256,2	K562	blood:
27	chr15:99974033..99977897-chr15:99978912..99982934,5	K562	blood:
28	chr15:99972525..99976931-chr15:99986719..99991606,5	MCF-7	breast:
29	chr15:99976374..99976897-chr15:100105314..100105862,2	Hela-S3	cervix:
30	chr15:99979583..99981872-chr15:99983556..99985309,2	MCF-7	breast:
31	chr15:99981180..99982961-chr15:99993073..99995315,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259341	TF binding region
ENSG00000259341	CpG island
ENSG00000068305	chromatin interactions

Extended variants
information (count: 859 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1561868	chr15:99972661-99972662	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537232785	chr15:99972677-99972678	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552480919	chr15:99972698-99972699	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571121559	chr15:99972713-99972714	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144024939	chr15:99972769-99972770	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553290414	chr15:99972782-99972783	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568465287	chr15:99972784-99972785	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188234945	chr15:99972863-99972864	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554819095	chr15:99972914-99972915	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs544830461	chr15:99972996-99972997	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2862151	chr15:99972999-99973000	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs527987308	chr15:99973023-99973024	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192519959	chr15:99973052-99973053	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540677049	chr15:99973067-99973068	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34367172	chr15:99973131-99973132	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201550059	chr15:99973164-99973165	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs530754305	chr15:99973171-99973172	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529757087	chr15:99973183-99973184	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs541560273	chr15:99973185-99973186	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs184393954	chr15:99973201-99973202	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548863988	chr15:99973202-99973203	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs562180728	chr15:99973215-99973216	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs371210638	chr15:99973248-99973249	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs557976811	chr15:99973249-99973250	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs74035732	chr15:99973286-99973287	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571066994	chr15:99973294-99973295	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528736267	chr15:99973367-99973368	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs7167464	chr15:99973369-99973370	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs568406426	chr15:99973393-99973394	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs535831914	chr15:99973399-99973400	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs7169461	chr15:99973413-99973414	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs569367113	chr15:99973436-99973437	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372228574	chr15:99973441-99973442	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115864870	chr15:99973450-99973451	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577088433	chr15:99973479-99973480	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs7169660	chr15:99973529-99973530	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs146710947	chr15:99973547-99973548	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs367587047	chr15:99973548-99973549	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs112372917	chr15:99973567-99973568	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs190525312	chr15:99973574-99973575	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs115502053	chr15:99973615-99973616	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs80084402	chr15:99973632-99973633	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs137989443	chr15:99973637-99973638	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs149474121	chr15:99973642-99973643	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564673548	chr15:99973658-99973659	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs551639829	chr15:99973683-99973684	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570219769	chr15:99973694-99973695	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537388608	chr15:99973710-99973711	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs181971010	chr15:99973727-99973728	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs143875849	chr15:99973741-99973742	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	20811773	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Emphysema	19352772	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17142309	CNVD
Schizophrenia	23813976	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99957200-99973200	Weak transcription	Gastric	stomach
2	chr15:99966400-99972800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr15:99966400-99973200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr15:99966400-99973400	Weak transcription	Hela-S3	cervix
5	chr15:99966400-99973600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:99966600-99973200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr15:99966800-99973200	Weak transcription	Stomach Mucosa	stomach
8	chr15:99966800-99975400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr15:99967200-99972800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr15:99967200-99972800	Weak transcription	Colonic Mucosa	Colon
11	chr15:99967200-99972800	Weak transcription	Lung	lung
12	chr15:99967600-99973200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr15:99970000-99976800	Enhancers	Primary B cells from peripheral blood	blood
14	chr15:99970400-99973200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr15:99970600-99973200	Weak transcription	Fetal Heart	heart
16	chr15:99971200-99974600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr15:99971200-99978000	Enhancers	Spleen	Spleen
18	chr15:99971400-99978800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr15:99971400-99979200	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr15:99971600-99973400	Enhancers	Primary T cells fromperipheralblood	blood
21	chr15:99971600-99973400	Weak transcription	NHEK	skin
22	chr15:99971600-99973600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr15:99971600-99978800	Enhancers	Primary T cells from cord blood	blood
24	chr15:99971800-99973000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr15:99971800-99973200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr15:99971800-99974000	Enhancers	Thymus	Thymus
27	chr15:99971800-99976400	Enhancers	Primary B cells from cord blood	blood
28	chr15:99972000-99973000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr15:99972000-99975200	Enhancers	Esophagus	oesophagus
30	chr15:99972000-99976000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr15:99972000-99976600	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr15:99972200-99973000	Weak transcription	Fetal Stomach	stomach
33	chr15:99972200-99974400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr15:99972200-99976200	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr15:99972200-99978600	Enhancers	Fetal Thymus	thymus
36	chr15:99972400-99974200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr15:99972400-99974400	Enhancers	Right Ventricle	heart
38	chr15:99972400-99975800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr15:99972400-99977400	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr15:99972600-99972800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr15:99972600-99973000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr15:99972600-99973000	Flanking Bivalent TSS/Enh	HepG2	liver
43	chr15:99972600-99974200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr15:99972600-99974200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr15:99972600-99974400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr15:99972600-99974400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr15:99972600-99975200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:99972600-99975200	Enhancers	HMEC	breast
49	chr15:99972600-99975600	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr15:99972600-99976400	Enhancers	HUES6 Cell Line	embryonic stem cell

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