Variant report

Variant	nsv1049055
Chromosome Location	chr15:52990467-53030603
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	chr15:53025336-53025762	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:53027711-53028005	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:53001404-53001641	HepG2	liver:	n/a	n/a
4	ATF3	chr15:53027706-53027979	K562	blood:	n/a	n/a
5	BATF	chr15:53027744-53028040	GM12878	blood:	n/a	chr15:53027945-53027954
6	BHLHE40	chr15:53027714-53028030	K562	blood:	n/a	n/a
7	BHLHE40	chr15:53027701-53028165	GM12878	blood:	n/a	n/a
8	BHLHE40	chr15:53022151-53022783	GM12878	blood:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
9	BHLHE40	chr15:53022405-53022675	HepG2	liver:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
10	BHLHE40	chr15:53022411-53022779	K562	blood:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
11	BRCA1	chr15:53003829-53003910	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr15:53021054-53021493	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr15:53027739-53028160	A549	lung:	n/a	n/a
14	CEBPB	chr15:53025362-53025763	Hela-S3	cervix:	n/a	chr15:53025567-53025578
15	CEBPB	chr15:53025384-53025753	HepG2	liver:	n/a	chr15:53025567-53025578
16	CEBPB	chr15:53007378-53007639	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:53012270-53012669	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr15:53025408-53025729	K562	blood:	n/a	chr15:53025567-53025578
19	CEBPB	chr15:53001315-53001704	HepG2	liver:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
20	CEBPB	chr15:53012468-53012470	A549	lung:	n/a	n/a
21	CEBPB	chr15:53021130-53021481	IMR90	lung:	n/a	n/a
22	CEBPB	chr15:53015920-53016153	A549	lung:	n/a	n/a
23	CEBPB	chr15:53001375-53001589	HepG2	liver:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
24	CEBPB	chr15:53025415-53025697	HepG2	liver:	n/a	chr15:53025567-53025578
25	CEBPB	chr15:53025447-53025711	HepG2	liver:	n/a	chr15:53025567-53025578
26	CEBPB	chr15:53015982-53016146	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr15:53001361-53001671	IMR90	lung:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
28	CEBPB	chr15:53001333-53001688	Hela-S3	cervix:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
29	CEBPB	chr15:53025372-53025801	HepG2	liver:	n/a	chr15:53025567-53025578
30	CEBPB	chr15:53021098-53021506	Hela-S3	cervix:	n/a	n/a
31	CEBPD	chr15:53025449-53025682	HepG2	liver:	n/a	chr15:53025568-53025579
32	CTCF	chr15:53027780-53027930	SAEC	small airway:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
33	CTCF	chr15:53027760-53027910	NHEK	skin:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
34	CTCF	chr15:53027533-53028284	SK-N-SH	brain:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
35	CTCF	chr15:53027820-53027970	HPAF	blood vessel:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
36	CTCF	chr15:53027840-53027990	HA-sp	spinal cord:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
37	CTCF	chr15:53027840-53027990	GM12865	blood:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
38	CTCF	chr15:53027761-53027990	LNCaP	prostate:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
39	CTCF	chr15:53022515-53022616	MCF-7	breast:	n/a	n/a
40	CTCF	chr15:53027820-53027970	HUVEC	blood vessel:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
41	CTCF	chr15:53027860-53028010	HRE	kidney:	n/a	chr15:53027866-53027879 chr15:53027865-53027881 chr15:53027864-53027882
42	CTCF	chr15:53027820-53027970	HMEC	breast:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
43	CTCF	chr15:53022514-53022630	Lung_OC	lung:	n/a	n/a
44	CTCF	chr15:53010060-53010210	GM12872	blood:	n/a	n/a
45	CTCF	chr15:53027788-53027945	GM12892	blood:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
46	CTCF	chr15:53027820-53027970	SK-N-SH_RA	brain:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
47	CTCF	chr15:53027780-53027930	GM12866	blood:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
48	CTCF	chr15:53027760-53027981	MCF-7	breast:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
49	CTCF	chr15:53027843-53027895	MCF-7	breast:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
50	CTCF	chr15:53027679-53028164	HCT-116	colon:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53001117-53001167	GM06990	blood:	n/a
2	chr15:53001117-53001167	HCM	heart:	n/a
3	chr15:53001117-53001167	HepG2	liver:	n/a
4	chr15:53001117-53001167	AG09319	gingival:	n/a
5	chr15:53001117-53001167	HEK293	kidney:	embryo
6	chr15:53001117-53001167	HNPCEpiC	eye:	n/a
7	chr15:53001117-53001167	IMR90	lung:	fetal
8	chr15:53001117-53001167	MCF-7	breast:	n/a
9	chr15:53001117-53001167	HCF	heart:	n/a
10	chr15:53001117-53001167	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:53001117-53001167	MCF10A-Er-Src	breast:	n/a
12	chr15:53001117-53001167	SK-N-MC	brain:	n/a
13	chr15:53001117-53001167	NHDF-neo	bronchial:	n/a
14	chr15:53001117-53001167	U87	brain:	n/a
15	chr15:53001117-53001167	RPTEC	kidney:	n/a
16	chr15:53001117-53001167	AG10803	skin:	n/a
17	chr15:53001117-53001167	AG04449	skin:	fetal
18	chr15:53001117-53001167	ECC-1	luminal epithelium:	n/a
19	chr15:53001117-53001167	SK-N-SH_RA	brain:	n/a
20	chr15:53001117-53001167	T-47D	breast:	n/a
21	chr15:53001117-53001167	BE2_C	brain:	n/a
22	chr15:53001117-53001167	GM12892	blood:	n/a
23	chr15:53001117-53001167	SKMC	muscle:	n/a
24	chr15:53001117-53001167	HRPEpiC	eye:	n/a
25	chr15:53001117-53001167	HUVEC	blood vessel:	n/a
26	chr15:53001117-53001167	AG04450	lung:	fetal
27	chr15:53001117-53001167	K562	blood:	n/a
28	chr15:53001117-53001167	HAEpiC	amniotic membrane:	n/a
29	chr15:53001117-53001167	BJ	skin:	n/a
30	chr15:53001117-53001167	Caco-2	colon:	n/a
31	chr15:53001117-53001167	ProgFib	skin:	n/a
32	chr15:53001117-53001167	AG09309	skin:	n/a
33	chr15:53001117-53001167	HMEC	breast:	n/a
34	chr15:53001117-53001167	ovcar-3	ovarian:	n/a
35	chr15:53001117-53001167	Jurkat	blood:	n/a
36	chr15:53001117-53001167	NH-A	brain:	n/a
37	chr15:53001117-53001167	GM19239	blood:	n/a
38	chr15:53001117-53001167	SK-N-SH	brain:	n/a
39	chr15:53001117-53001167	PrEC	prostate:	n/a
40	chr15:53001117-53001167	HIPEpiC	eye:	n/a
41	chr15:53001117-53001167	SAEC	small airway:	n/a
42	chr15:53001117-53001167	LNCaP	prostate:	n/a
43	chr15:53001117-53001167	Hela-S3	cervix:	n/a
44	chr15:53001117-53001167	HCT-116	colon:	n/a
45	chr15:53001117-53001167	A549	lung:	n/a
46	chr15:53001117-53001167	HRCEpiC	kidney:	n/a
47	chr15:53001117-53001167	H1-hESC	embryonic stem cell:	embryo
48	chr15:53001117-53001167	PANC-1	pancreas:	n/a
49	chr15:53001117-53001167	PFSK-1	brain:	n/a
50	chr15:53001117-53001167	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:52990279..52992923-chr15:53000630..53003085,2	MCF-7	breast:
2	chr15:52859015..52862196-chr15:53026182..53028979,3	MCF-7	breast:
3	chr15:52942373..52946105-chr15:53022429..53026141,4	MCF-7	breast:
4	chr15:52986948..52989428-chr15:52996280..52998700,2	MCF-7	breast:
5	chr15:52623330..52624257-chr15:53027398..53028338,3	K562	blood:
6	chr15:52844953..52847640-chr15:53010163..53013098,2	MCF-7	breast:
7	chr15:52990867..52992596-chr15:52999678..53002178,2	MCF-7	breast:
8	chr15:52969966..52973260-chr15:53007866..53011792,4	MCF-7	breast:
9	chr15:53001798..53003547-chr15:53015558..53017626,2	MCF-7	breast:
10	chr15:52966586..52968208-chr15:53018199..53019999,2	MCF-7	breast:
11	chr15:53014375..53016603-chr15:53017308..53019885,2	MCF-7	breast:
12	chr15:52509083..52509697-chr15:53027309..53027962,2	MCF-7	breast:
13	chr15:53002359..53006038-chr15:53007315..53009805,4	K562	blood:
14	chr15:52970778..52973073-chr15:53012277..53014291,2	MCF-7	breast:
15	chr15:52968697..52973342-chr15:53018163..53028590,24	MCF-7	breast:
16	chr15:53020023..53021825-chr15:53025584..53028001,2	MCF-7	breast:
17	chr15:52967780..52973455-chr15:53015921..53024493,22	MCF-7	breast:
18	chr15:52969340..52972976-chr15:53024542..53030044,12	MCF-7	breast:
19	chr15:52991504..52994033-chr15:53002922..53004759,2	MCF-7	breast:
20	chr15:53022444..53024405-chr15:53025609..53027744,2	MCF-7	breast:
21	chr15:52628155..52629955-chr15:53015410..53018106,2	MCF-7	breast:
22	chr15:53001338..53004194-chr15:53026134..53027960,2	MCF-7	breast:
23	chr15:52529115..52532047-chr15:52992666..52994402,2	K562	blood:
24	chr15:53002359..53006038-chr15:53007315..53009805,4	K562	blood:
25	chr15:52548200..52549159-chr15:53027337..53028329,9	MCF-7	breast:
26	chr15:52987035..52988935-chr15:53020479..53022010,2	MCF-7	breast:
27	chr15:52967401..52973659-chr15:53000765..53004676,11	MCF-7	breast:
28	chr15:52587244..52588799-chr15:53018696..53021344,2	MCF-7	breast:
29	chr15:53008460..53014321-chr15:53016290..53019599,5	MCF-7	breast:
30	chr15:52623345..52624286-chr15:53022394..53023020,2	MCF-7	breast:
31	chr15:52991521..52993410-chr15:52996311..52999236,2	MCF-7	breast:
32	chr15:53014375..53016603-chr15:53017308..53019885,2	MCF-7	breast:
33	chr15:52979304..52981911-chr15:53011644..53013861,2	MCF-7	breast:
34	chr15:53020211..53022742-chr15:53022811..53024880,2	MCF-7	breast:
35	chr15:52819938..52821534-chr15:53026653..53028952,2	MCF-7	breast:
36	chr15:53017085..53018702-chr15:53021319..53022831,2	MCF-7	breast:
37	chr15:52981751..52983702-chr15:52997065..52999540,2	MCF-7	breast:
38	chr15:52991504..52994033-chr15:53002922..53004759,2	MCF-7	breast:
39	chr15:53020211..53022742-chr15:53022811..53024880,2	MCF-7	breast:
40	chr15:53020023..53021825-chr15:53025584..53028001,2	MCF-7	breast:
41	chr15:52548546..52549086-chr15:53027357..53028249,2	MCF-7	breast:
42	chr15:52991521..52993410-chr15:52996311..52999236,2	MCF-7	breast:
43	chr15:52978223..52981172-chr15:53005234..53007666,2	MCF-7	breast:
44	chr15:52970614..52972574-chr15:53011299..53014236,2	MCF-7	breast:
45	chr15:52970785..52973289-chr15:52989894..52992912,4	MCF-7	breast:
46	chr15:52973784..52977367-chr15:53024530..53026901,4	MCF-7	breast:
47	chr15:52623273..52624277-chr15:53027279..53028330,7	MCF-7	breast:
48	chr15:52508008..52509939-chr15:53026331..53028847,2	MCF-7	breast:
49	chr15:53008460..53014321-chr15:53016290..53019599,5	MCF-7	breast:
50	chr15:52968259..52973250-chr15:52997483..53005703,18	MCF-7	breast:

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

Extended variants
information (count: 1560 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1560 , 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	rs532512141	chr15:52990484-52990485	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs180984095	chr15:52990560-52990561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548813546	chr15:52990583-52990584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183471487	chr15:52990639-52990640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537616894	chr15:52990654-52990655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552434732	chr15:52990701-52990702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs4575480	chr15:52990823-52990824	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs80236108	chr15:52990861-52990862	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs534713796	chr15:52990943-52990944	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs4254271	chr15:52990946-52990947	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs574408523	chr15:52990956-52990957	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs535338218	chr15:52990995-52990996	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs188591154	chr15:52991023-52991024	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144367374	chr15:52991057-52991058	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs199603211	chr15:52991124-52991125	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545969162	chr15:52991131-52991132	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181174890	chr15:52991187-52991188	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs111462129	chr15:52991217-52991218	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539855231	chr15:52991260-52991261	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148800796	chr15:52991290-52991291	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530437277	chr15:52991311-52991312	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542566234	chr15:52991314-52991315	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563953709	chr15:52991315-52991316	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186060843	chr15:52991402-52991403	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552695270	chr15:52991417-52991418	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141505618	chr15:52991469-52991470	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368084154	chr15:52991520-52991521	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs190411194	chr15:52991566-52991567	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs112529159	chr15:52991582-52991583	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200792073	chr15:52991591-52991592	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs113956796	chr15:52991625-52991626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115878398	chr15:52991632-52991633	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76216286	chr15:52991677-52991678	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539645079	chr15:52991783-52991784	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111845494	chr15:52991792-52991793	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187470559	chr15:52991796-52991797	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539259766	chr15:52991823-52991824	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112577416	chr15:52991829-52991830	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs16965128	chr15:52991859-52991860	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs540293380	chr15:52991863-52991864	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs551565609	chr15:52991901-52991902	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555477785	chr15:52991948-52991949	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573711449	chr15:52991957-52991958	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191874204	chr15:52992005-52992006	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146372156	chr15:52992012-52992013	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs531196415	chr15:52992028-52992029	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546099324	chr15:52992052-52992053	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139606750	chr15:52992141-52992142	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528657601	chr15:52992145-52992146	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547105418	chr15:52992183-52992184	Enhancers Weak transcription	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:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52979200-52991400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr15:52979400-52991600	Weak transcription	Primary B cells from cord blood	blood
3	chr15:52982600-52993200	Weak transcription	Liver	Liver
4	chr15:52990200-52991200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:52990400-52990600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr15:52990400-52991600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr15:52990600-52991200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:52990800-52991000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr15:52990800-52991200	Enhancers	A549	lung
10	chr15:52990800-52991400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr15:52991000-52991600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr15:52991200-52991400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:52991200-52991600	Enhancers	Fetal Kidney	kidney
14	chr15:52991200-52992200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:52991400-52992000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:52991400-52995000	Enhancers	Primary B cells from peripheral blood	blood
17	chr15:52991400-52997800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:52991600-52992000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr15:52991600-52992000	Enhancers	Primary B cells from cord blood	blood
20	chr15:52992000-52992600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr15:52992000-52993400	Weak transcription	Primary B cells from cord blood	blood
22	chr15:52993200-52993600	Enhancers	Liver	Liver
23	chr15:52993400-52994400	Enhancers	Primary B cells from cord blood	blood
24	chr15:52993600-52994600	Weak transcription	Liver	Liver
25	chr15:52994600-52995800	Enhancers	Liver	Liver
26	chr15:52995000-52999600	Weak transcription	Primary B cells from peripheral blood	blood
27	chr15:52995400-52995800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr15:52995800-52998200	Weak transcription	Liver	Liver
29	chr15:52995800-53001600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr15:52997800-52998800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:52998200-52998400	Enhancers	Liver	Liver
32	chr15:52998200-52998800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:52998200-52998800	Enhancers	NHEK	skin
34	chr15:52998200-52999200	Enhancers	Muscle Satellite Cultured Cells	--
35	chr15:52998200-52999400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr15:52998400-52998800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr15:52998400-52999000	Flanking Active TSS	Liver	Liver
38	chr15:52998400-52999000	Enhancers	HSMM	muscle
39	chr15:52998800-53000800	Enhancers	Primary B cells from cord blood	blood
40	chr15:52998800-53001000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr15:52998800-53001200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr15:52998800-53001600	Weak transcription	NHEK	skin
43	chr15:52998800-53002200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr15:52999000-52999200	Active TSS	Liver	Liver
45	chr15:52999200-52999400	Flanking Active TSS	Liver	Liver
46	chr15:52999400-52999800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:52999400-53000200	Active TSS	Liver	Liver
48	chr15:52999600-53001000	Enhancers	Primary B cells from peripheral blood	blood
49	chr15:52999800-53001200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr15:53000200-53000800	Flanking Active TSS	Liver	Liver

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