Variant report

Variant	nsv1054289
Chromosome Location	chr15:76437970-76485966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1613)
CpG islands
(count:1343)
Chromatin interactive
region (count:65)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76443498-76443553	K562	blood:	n/a	n/a
2	ARID3A	chr15:76443358-76443550	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76483064-76483427	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:76478041-76478258	HepG2	liver:	n/a	n/a
5	ATF2	chr15:76473954-76474425	GM12878	blood:	n/a	n/a
6	ATF2	chr15:76483089-76483813	GM12878	blood:	n/a	n/a
7	ATF2	chr15:76473823-76474454	GM12878	blood:	n/a	n/a
8	ATF2	chr15:76443260-76443649	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:76443272-76443758	GM12878	blood:	n/a	n/a
10	ATF3	chr15:76461499-76461617	GM12878	blood:	n/a	n/a
11	ATF3	chr15:76461359-76461682	GM12878	blood:	n/a	n/a
12	ATF3	chr15:76461421-76461690	K562	blood:	n/a	n/a
13	ATF3	chr15:76461375-76461737	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:76483297-76483365	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr15:76473923-76474319	GM12878	blood:	n/a	chr15:76474119-76474130
16	BATF	chr15:76443332-76443766	GM12878	blood:	n/a	chr15:76443610-76443620
17	BATF	chr15:76473865-76474455	GM12878	blood:	n/a	chr15:76474119-76474130
18	BATF	chr15:76443394-76443743	GM12878	blood:	n/a	chr15:76443610-76443620
19	BCL11A	chr15:76473914-76474363	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:76443407-76443717	GM12878	blood:	n/a	n/a
21	BCL11A	chr15:76474032-76474320	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:76443382-76443708	GM12878	blood:	n/a	n/a
23	BCL3	chr15:76482892-76483810	A549	lung:	n/a	n/a
24	BCLAF1	chr15:76473788-76474517	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:76473905-76474445	GM12878	blood:	n/a	n/a
26	BCLAF1	chr15:76443247-76443763	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:76440299-76440592	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:76482536-76482865	K562	blood:	n/a	n/a
29	BHLHE40	chr15:76483088-76483437	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:76472787-76472910	K562	blood:	n/a	n/a
31	BHLHE40	chr15:76443352-76443674	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:76472876-76472910	HepG2	liver:	n/a	n/a
33	BHLHE40	chr15:76483122-76483431	K562	blood:	n/a	n/a
34	BHLHE40	chr15:76455772-76455880	K562	blood:	n/a	n/a
35	BHLHE40	chr15:76443337-76443588	K562	blood:	n/a	n/a
36	BHLHE40	chr15:76473924-76474330	GM12878	blood:	n/a	n/a
37	BHLHE40	chr15:76469949-76470149	A549	lung:	n/a	n/a
38	BRCA1	chr15:76483167-76483490	HepG2	liver:	n/a	chr15:76483441-76483448
39	BRCA1	chr15:76483134-76483378	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr15:76483097-76483525	Hela-S3	cervix:	n/a	chr15:76483441-76483448
41	BRCA1	chr15:76440353-76440459	HepG2	liver:	n/a	n/a
42	BRCA1	chr15:76455813-76456207	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr15:76477995-76478351	K562	blood:	n/a	n/a
44	CEBPB	chr15:76455706-76456096	HepG2	liver:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
45	CEBPB	chr15:76482808-76483429	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr15:76455169-76456214	Hela-S3	cervix:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
47	CEBPB	chr15:76482803-76483407	MCF-7	breast:	n/a	n/a
48	CEBPB	chr15:76475123-76475449	IMR90	lung:	n/a	n/a
49	CEBPB	chr15:76443340-76443572	K562	blood:	n/a	n/a
50	CEBPB	chr15:76441608-76442115	IMR90	lung:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76475969-76476019	ProgFib	skin:	n/a
2	chr15:76475969-76476019	ProgFib	skin:	n/a
3	chr15:76480434-76480484	SK-N-SH_RA	brain:	n/a
4	chr15:76455848-76455898	SKMC	muscle:	n/a
5	chr15:76483281-76483331	HEEpiC	esophagus:	n/a
6	chr15:76444525-76444575	HRPEpiC	eye:	n/a
7	chr15:76458372-76458422	HEK293	kidney:	embryo
8	chr15:76483344-76483394	HMEC	breast:	n/a
9	chr15:76458279-76458329	HepG2	liver:	n/a
10	chr15:76440448-76440498	HNPCEpiC	eye:	n/a
11	chr15:76483281-76483331	BE2_C	brain:	n/a
12	chr15:76483281-76483331	Hela-S3	cervix:	n/a
13	chr15:76440405-76440455	LNCaP	prostate:	n/a
14	chr15:76462821-76462871	HIPEpiC	eye:	n/a
15	chr15:76440448-76440498	ProgFib	skin:	n/a
16	chr15:76484473-76484523	HMEC	breast:	n/a
17	chr15:76484473-76484523	MCF10A-Er-Src	breast:	n/a
18	chr15:76442477-76442527	K562	blood:	n/a
19	chr15:76461960-76462010	HCT-116	colon:	n/a
20	chr15:76484625-76484675	SK-N-MC	brain:	n/a
21	chr15:76440448-76440498	SK-N-SH	brain:	n/a
22	chr15:76484379-76484429	SKMC	muscle:	n/a
23	chr15:76480434-76480484	GM06990	blood:	n/a
24	chr15:76483281-76483331	HL-60	blood:	n/a
25	chr15:76461960-76462010	HMEC	breast:	n/a
26	chr15:76462821-76462871	ProgFib	skin:	n/a
27	chr15:76483201-76483251	ProgFib	skin:	n/a
28	chr15:76444525-76444575	LNCaP	prostate:	n/a
29	chr15:76484102-76484152	NHDF-neo	bronchial:	n/a
30	chr15:76470979-76471029	A549	lung:	n/a
31	chr15:76483201-76483251	HNPCEpiC	eye:	n/a
32	chr15:76483344-76483394	LNCaP	prostate:	n/a
33	chr15:76455848-76455898	NT2-D1	testis:	n/a
34	chr15:76478102-76478152	HRE	kidney:	n/a
35	chr15:76484102-76484152	NT2-D1	testis:	n/a
36	chr15:76462821-76462871	HRE	kidney:	n/a
37	chr15:76461960-76462010	NT2-D1	testis:	n/a
38	chr15:76483344-76483394	SAEC	small airway:	n/a
39	chr15:76478102-76478152	HMEC	breast:	n/a
40	chr15:76484102-76484152	HL-60	blood:	n/a
41	chr15:76440405-76440455	HUVEC	blood vessel:	n/a
42	chr15:76484473-76484523	NHDF-neo	bronchial:	n/a
43	chr15:76480434-76480484	K562	blood:	n/a
44	chr15:76440448-76440498	HepG2	liver:	n/a
45	chr15:76484625-76484675	HIPEpiC	eye:	n/a
46	chr15:76458372-76458422	NHDF-neo	bronchial:	n/a
47	chr15:76440443-76440493	K562	blood:	n/a
48	chr15:76444525-76444575	Caco-2	colon:	n/a
49	chr15:76440443-76440493	SAEC	small airway:	n/a
50	chr15:76455848-76455898	H1-hESC	embryonic stem cell:	embryo

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:76482846..76483696-chr15:76577399..76578194,4	MCF-7	breast:
2	chr15:76446927..76448705-chr15:76450684..76453682,2	MCF-7	breast:
3	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
4	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
5	chr15:76478027..76479862-chr15:76483019..76485634,3	MCF-7	breast:
6	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
7	chr15:76482840..76483720-chr15:77132911..77133894,4	MCF-7	breast:
8	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
9	chr15:76452254..76455049-chr15:76455599..76457140,2	K562	blood:
10	chr15:76431477..76432448-chr15:76439936..76440516,2	K562	blood:
11	chr15:76435308..76437788-chr15:76443138..76445810,3	K562	blood:
12	chr15:76482924..76483751-chr15:76625816..76626899,5	MCF-7	breast:
13	chr15:76442105..76446396-chr15:76447199..76450761,5	MCF-7	breast:
14	chr15:76484853..76487491-chr15:76488798..76492049,5	K562	blood:
15	chr15:76477747..76478594-chr15:76625784..76626375,2	MCF-7	breast:
16	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
17	chr15:76461088..76462629-chr15:76483253..76485151,2	K562	blood:
18	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
19	chr15:76453204..76454747-chr15:76459797..76461438,2	MCF-7	breast:
20	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
21	chr15:76482740..76483457-chr15:76626133..76626814,2	MCF-7	breast:
22	chr15:76453204..76454747-chr15:76459797..76461438,2	MCF-7	breast:
23	chr15:76439768..76440654-chr15:77152468..77153214,2	K562	blood:
24	chr15:76349477..76350031-chr15:76443009..76443529,2	K562	blood:
25	chr15:76436435..76439411-chr15:76454805..76456724,2	K562	blood:
26	chr15:76484065..76486868-chr15:76602060..76604082,2	MCF-7	breast:
27	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
28	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
29	chr15:76483246..76483790-chr15:77158830..77159724,2	K562	blood:
30	chr15:76482420..76485297-chr15:76485451..76488299,2	K562	blood:
31	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
32	chr15:76452837..76455028-chr15:76460465..76463193,2	K562	blood:
33	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
34	chr15:76483023..76483731-chr15:76527305..76528242,4	MCF-7	breast:
35	chr15:76452837..76455028-chr15:76460465..76463193,2	K562	blood:
36	chr15:76478149..76479732-chr15:76481760..76484387,3	K562	blood:
37	chr15:76482829..76483665-chr15:77158796..77159907,4	MCF-7	breast:
38	chr15:76102073..76103015-chr15:76443067..76443572,2	MCF-7	breast:
39	chr15:76446927..76448705-chr15:76450684..76453682,2	MCF-7	breast:
40	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
41	chr15:76482820..76483740-chr15:76577311..76578273,3	K562	blood:
42	chr15:76482702..76486394-chr15:76633656..76636389,3	K562	blood:
43	chr15:76481529..76484202-chr15:76633877..76636476,2	K562	blood:
44	chr15:76440836..76444169-chr15:76451014..76453553,3	MCF-7	breast:
45	chr15:76436946..76439521-chr3:195163273..195165269,2	MCF-7	breast:
46	chr15:76457780..76460448-chr15:76461142..76462656,2	K562	blood:
47	chr15:76478115..76478633-chr15:76622409..76623267,2	MCF-7	breast:
48	chr15:76452254..76455049-chr15:76455599..76457140,2	K562	blood:
49	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
50	chr15:76440836..76444169-chr15:76451014..76453553,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259422	TF binding region
C15orf27	TF binding region
ENSG00000259422	CpG island
C15orf27	CpG island
ENSG00000169758	chromatin interactions
ENSG00000159556	chromatin interactions
ENSG00000259514	chromatin interactions
ENSG00000259422	chromatin interactions
ENSG00000169752	chromatin interactions
ENSG00000270036	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000114331	chromatin interactions

Extended variants
information (count: 1908 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1908 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2935969	chr15:76437970-76437971	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs8043371	chr15:76437983-76437984	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs553144919	chr15:76437998-76437999	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369970477	chr15:76438022-76438023	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531351620	chr15:76438063-76438064	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572456203	chr15:76438070-76438071	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189144428	chr15:76438082-76438083	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs117545653	chr15:76438169-76438170	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531311306	chr15:76438237-76438238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549481739	chr15:76438243-76438244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565005393	chr15:76438279-76438280	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141858480	chr15:76438347-76438348	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs34448076	chr15:76438387-76438388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs150602432	chr15:76438413-76438414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574597747	chr15:76438423-76438424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs565876931	chr15:76438424-76438425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536585605	chr15:76438465-76438466	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548482805	chr15:76438468-76438469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200702891	chr15:76438504-76438505	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs117838217	chr15:76438527-76438528	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564536187	chr15:76438558-76438559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538254396	chr15:76438559-76438560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556245984	chr15:76438563-76438564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181125058	chr15:76438601-76438602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139702603	chr15:76438641-76438642	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs76395198	chr15:76438649-76438650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377450991	chr15:76438663-76438664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541954026	chr15:76438686-76438687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572288042	chr15:76438777-76438778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs555864411	chr15:76438797-76438798	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567135971	chr15:76438823-76438824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs561645898	chr15:76438835-76438836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576624065	chr15:76438888-76438889	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543414596	chr15:76438905-76438906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373566043	chr15:76438952-76438953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149789064	chr15:76438963-76438964	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532292305	chr15:76438966-76438967	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs72736819	chr15:76438993-76438994	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs559615976	chr15:76439009-76439010	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529936988	chr15:76439079-76439080	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190982990	chr15:76439109-76439110	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs569944121	chr15:76439131-76439132	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2935968	chr15:76439135-76439136	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs550197278	chr15:76439156-76439157	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs56036713	chr15:76439190-76439191	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538784979	chr15:76439194-76439195	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs553824833	chr15:76439198-76439199	Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574160565	chr15:76439242-76439243	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565805242	chr15:76439248-76439249	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs145779129	chr15:76439279-76439280	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Intellectual disability	22102821	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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:1280 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76429400-76442800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr15:76429600-76442800	Weak transcription	Brain Angular Gyrus	brain
3	chr15:76432400-76440400	Weak transcription	Pancreas	Pancrea
4	chr15:76432400-76442800	Weak transcription	Gastric	stomach
5	chr15:76432600-76440400	Weak transcription	Placenta	Placenta
6	chr15:76432600-76442800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr15:76433000-76439600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr15:76433000-76440400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr15:76433000-76442800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr15:76433000-76452800	Weak transcription	Right Atrium	heart
11	chr15:76433200-76440600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr15:76433600-76439800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr15:76433600-76440400	Weak transcription	Spleen	Spleen
14	chr15:76436600-76438200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr15:76436800-76438400	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr15:76437200-76439200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr15:76437400-76438000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr15:76437800-76438000	Flanking Active TSS	GM12878-XiMat	blood
19	chr15:76437800-76440400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr15:76438000-76438200	Enhancers	GM12878-XiMat	blood
21	chr15:76438200-76440400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr15:76438200-76442400	Weak transcription	GM12878-XiMat	blood
23	chr15:76438400-76439200	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr15:76439000-76439200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:76439000-76439400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:76439000-76439800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr15:76439200-76439600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr15:76439200-76439800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:76439200-76439800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr15:76439200-76440200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr15:76439200-76441400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr15:76439400-76439600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr15:76439400-76439600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:76439400-76439600	Enhancers	HMEC	breast
35	chr15:76439400-76440400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr15:76439600-76439800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr15:76439600-76440200	Weak transcription	HMEC	breast
38	chr15:76439600-76440400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr15:76439800-76440200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr15:76439800-76440200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr15:76439800-76440800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr15:76439800-76442800	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr15:76440000-76440800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr15:76440000-76442600	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr15:76440200-76440400	Enhancers	HMEC	breast
46	chr15:76440200-76440600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr15:76440200-76440800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:76440200-76441000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:76440400-76440600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr15:76440400-76440600	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood

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