Variant report

Variant	nsv1036319
Chromosome Location	chr15:76432823-76489955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1842)
CpG islands
(count:1344)
Chromatin interactive
region (count:76)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1842 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76483064-76483427	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76443358-76443550	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76488758-76489089	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:76443498-76443553	K562	blood:	n/a	n/a
5	ARID3A	chr15:76478041-76478258	HepG2	liver:	n/a	n/a
6	ATF2	chr15:76473954-76474425	GM12878	blood:	n/a	n/a
7	ATF2	chr15:76443260-76443649	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:76443272-76443758	GM12878	blood:	n/a	n/a
9	ATF2	chr15:76473823-76474454	GM12878	blood:	n/a	n/a
10	ATF2	chr15:76483089-76483813	GM12878	blood:	n/a	n/a
11	ATF3	chr15:76461375-76461737	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr15:76461359-76461682	GM12878	blood:	n/a	n/a
13	ATF3	chr15:76488695-76489271	A549	lung:	n/a	n/a
14	ATF3	chr15:76461421-76461690	K562	blood:	n/a	n/a
15	ATF3	chr15:76461499-76461617	GM12878	blood:	n/a	n/a
16	BACH1	chr15:76483297-76483365	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr15:76443394-76443743	GM12878	blood:	n/a	chr15:76443610-76443620
18	BATF	chr15:76473923-76474319	GM12878	blood:	n/a	chr15:76474119-76474130
19	BATF	chr15:76473865-76474455	GM12878	blood:	n/a	chr15:76474119-76474130
20	BATF	chr15:76443332-76443766	GM12878	blood:	n/a	chr15:76443610-76443620
21	BCL11A	chr15:76443407-76443717	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:76473914-76474363	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:76474032-76474320	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:76443382-76443708	GM12878	blood:	n/a	n/a
25	BCL3	chr15:76488403-76489359	A549	lung:	n/a	n/a
26	BCL3	chr15:76482892-76483810	A549	lung:	n/a	n/a
27	BCLAF1	chr15:76443247-76443763	GM12878	blood:	n/a	n/a
28	BCLAF1	chr15:76473788-76474517	GM12878	blood:	n/a	n/a
29	BCLAF1	chr15:76473905-76474445	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:76443337-76443588	K562	blood:	n/a	n/a
31	BHLHE40	chr15:76443352-76443674	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:76455772-76455880	K562	blood:	n/a	n/a
33	BHLHE40	chr15:76472876-76472910	HepG2	liver:	n/a	n/a
34	BHLHE40	chr15:76473924-76474330	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:76483088-76483437	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:76472787-76472910	K562	blood:	n/a	n/a
37	BHLHE40	chr15:76482536-76482865	K562	blood:	n/a	n/a
38	BHLHE40	chr15:76440299-76440592	GM12878	blood:	n/a	n/a
39	BHLHE40	chr15:76483122-76483431	K562	blood:	n/a	n/a
40	BHLHE40	chr15:76486297-76486653	K562	blood:	n/a	n/a
41	BHLHE40	chr15:76488854-76489227	K562	blood:	n/a	n/a
42	BHLHE40	chr15:76486294-76486734	HepG2	liver:	n/a	n/a
43	BHLHE40	chr15:76469949-76470149	A549	lung:	n/a	n/a
44	BRCA1	chr15:76455813-76456207	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr15:76483167-76483490	HepG2	liver:	n/a	chr15:76483441-76483448
46	BRCA1	chr15:76483097-76483525	Hela-S3	cervix:	n/a	chr15:76483441-76483448
47	BRCA1	chr15:76440353-76440459	HepG2	liver:	n/a	n/a
48	BRCA1	chr15:76483134-76483378	H1-hESC	embryonic stem cell:	n/a	n/a
49	CBX3	chr15:76488727-76489226	K562	blood:	n/a	n/a
50	CBX3	chr15:76477995-76478351	K562	blood:	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	chr15:76442477-76442527	GM12892	blood:	n/a
2	chr15:76462821-76462871	HCT-116	colon:	n/a
3	chr15:76442477-76442527	GM12892	blood:	n/a
4	chr15:76462821-76462871	HCT-116	colon:	n/a
5	chr15:76461960-76462010	HEEpiC	esophagus:	n/a
6	chr15:76480434-76480484	HMEC	breast:	n/a
7	chr15:76484625-76484675	HCM	heart:	n/a
8	chr15:76440448-76440498	Jurkat	blood:	n/a
9	chr15:76444525-76444575	AG10803	skin:	n/a
10	chr15:76480434-76480484	NHBE	bronchial:	n/a
11	chr15:76444525-76444575	AoSMC	blood vessel:	n/a
12	chr15:76440448-76440498	H1-hESC	embryonic stem cell:	embryo
13	chr15:76440443-76440493	Hepatocyte	liver:	n/a
14	chr15:76440448-76440498	T-47D	breast:	n/a
15	chr15:76455848-76455898	RPTEC	kidney:	n/a
16	chr15:76444525-76444575	HUVEC	blood vessel:	n/a
17	chr15:76455848-76455898	ECC-1	luminal epithelium:	n/a
18	chr15:76484473-76484523	PANC-1	pancreas:	n/a
19	chr15:76484102-76484152	Hela-S3	cervix:	n/a
20	chr15:76442477-76442527	IMR90	lung:	fetal
21	chr15:76484102-76484152	GM12891	blood:	n/a
22	chr15:76458372-76458422	MCF-7	breast:	n/a
23	chr15:76442477-76442527	BJ	skin:	n/a
24	chr15:76483344-76483394	HCT-116	colon:	n/a
25	chr15:76455848-76455898	AG04450	lung:	fetal
26	chr15:76458365-76458415	RPTEC	kidney:	n/a
27	chr15:76458372-76458422	K562	blood:	n/a
28	chr15:76458372-76458422	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:76440443-76440493	HEEpiC	esophagus:	n/a
30	chr15:76483201-76483251	HEK293	kidney:	embryo
31	chr15:76484102-76484152	PANC-1	pancreas:	n/a
32	chr15:76480434-76480484	HIPEpiC	eye:	n/a
33	chr15:76458365-76458415	AoSMC	blood vessel:	n/a
34	chr15:76475969-76476019	GM12892	blood:	n/a
35	chr15:76483281-76483331	GM12892	blood:	n/a
36	chr15:76484379-76484429	IMR90	lung:	fetal
37	chr15:76480434-76480484	A549	lung:	n/a
38	chr15:76483201-76483251	AoSMC	blood vessel:	n/a
39	chr15:76484625-76484675	AG04449	skin:	fetal
40	chr15:76478102-76478152	MCF-7	breast:	n/a
41	chr15:76458279-76458329	HCPEpiC	choroid plexus:	n/a
42	chr15:76440405-76440455	HIPEpiC	eye:	n/a
43	chr15:76458279-76458329	CMK	blood:	n/a
44	chr15:76480434-76480484	HCT-116	colon:	n/a
45	chr15:76484102-76484152	HCM	heart:	n/a
46	chr15:76458279-76458329	MCF10A-Er-Src	breast:	n/a
47	chr15:76462821-76462871	RPTEC	kidney:	n/a
48	chr15:76484102-76484152	BE2_C	brain:	n/a
49	chr15:76475969-76476019	AoSMC	blood vessel:	n/a
50	chr15:76461960-76462010	AoSMC	blood vessel:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
2	chr15:76482846..76483696-chr15:76577399..76578194,4	MCF-7	breast:
3	chr15:76482924..76483751-chr15:76625816..76626899,5	MCF-7	breast:
4	chr15:76442105..76446396-chr15:76447199..76450761,5	MCF-7	breast:
5	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
6	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
7	chr15:76452254..76455049-chr15:76455599..76457140,2	K562	blood:
8	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
9	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
10	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
11	chr15:76453204..76454747-chr15:76459797..76461438,2	MCF-7	breast:
12	chr15:76482840..76483720-chr15:77132911..77133894,4	MCF-7	breast:
13	chr15:76478115..76478633-chr15:76622409..76623267,2	MCF-7	breast:
14	chr15:76483018..76483722-chr15:76622624..76623279,3	K562	blood:
15	chr15:76477747..76478594-chr15:76625784..76626375,2	MCF-7	breast:
16	chr15:76349376..76350531-chr15:76431524..76433402,8	MCF-7	breast:
17	chr15:76478027..76479862-chr15:76483019..76485634,3	MCF-7	breast:
18	chr15:76102073..76103015-chr15:76443067..76443572,2	MCF-7	breast:
19	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
20	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
21	chr15:76440836..76444169-chr15:76451014..76453553,3	MCF-7	breast:
22	chr15:76440836..76444169-chr15:76451014..76453553,3	MCF-7	breast:
23	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
24	chr15:76439768..76440654-chr15:77152468..77153214,2	K562	blood:
25	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
26	chr15:76482820..76483740-chr15:76577311..76578273,3	K562	blood:
27	chr15:76435308..76437788-chr15:76443138..76445810,3	K562	blood:
28	chr15:76482740..76483457-chr15:76626133..76626814,2	MCF-7	breast:
29	chr15:76489752..76492594-chr15:76628754..76630476,2	K562	blood:
30	chr15:76349862..76350383-chr15:76442992..76443858,2	MCF-7	breast:
31	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
32	chr15:76486525..76491130-chr15:76491292..76495169,6	MCF-7	breast:
33	chr15:76446927..76448705-chr15:76450684..76453682,2	MCF-7	breast:
34	chr15:76221299..76222193-chr15:76443491..76444002,2	MCF-7	breast:
35	chr15:76436946..76439521-chr3:195163273..195165269,2	MCF-7	breast:
36	chr15:76478149..76479732-chr15:76481760..76484387,3	K562	blood:
37	chr15:76482829..76483665-chr15:77158796..77159907,4	MCF-7	breast:
38	chr15:76484853..76487491-chr15:76488798..76492049,5	K562	blood:
39	chr15:76349477..76350031-chr15:76443009..76443529,2	K562	blood:
40	chr15:76436435..76439411-chr15:76454805..76456724,2	K562	blood:
41	chr15:76484065..76486868-chr15:76602060..76604082,2	MCF-7	breast:
42	chr15:76487373..76491413-chr15:76492592..76495149,4	K562	blood:
43	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
44	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
45	chr15:76457780..76460448-chr15:76461142..76462656,2	K562	blood:
46	chr15:76453204..76454747-chr15:76459797..76461438,2	MCF-7	breast:
47	chr15:76483023..76483731-chr15:76527305..76528242,4	MCF-7	breast:
48	chr15:76489717..76491571-chr15:76503812..76506764,2	K562	blood:
49	chr15:76452254..76455049-chr15:76455599..76457140,2	K562	blood:
50	chr15:76446927..76448705-chr15:76450684..76453682,2	MCF-7	breast:

No data

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

Extended variants
information (count: 2259 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12441886	chr15:76432823-76432824	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370665286	chr15:76432842-76432843	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546694476	chr15:76432851-76432852	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568027033	chr15:76432855-76432856	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373817656	chr15:76432922-76432923	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543794125	chr15:76432950-76432951	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565549409	chr15:76432998-76432999	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577432646	chr15:76433000-76433001	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs78815538	chr15:76433018-76433019	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535111880	chr15:76433029-76433030	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs147165865	chr15:76433050-76433051	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74676835	chr15:76433082-76433083	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112069047	chr15:76433138-76433139	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556517635	chr15:76433139-76433140	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563511824	chr15:76433141-76433142	Weak transcription Enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200502958	chr15:76433213-76433214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs377182566	chr15:76433225-76433226	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs77157433	chr15:76433228-76433229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs62028658	chr15:76433230-76433231	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113147916	chr15:76433237-76433238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552060672	chr15:76433246-76433247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570738043	chr15:76433248-76433249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534572221	chr15:76433379-76433380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116088661	chr15:76433402-76433403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565731455	chr15:76433496-76433497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190365318	chr15:76433572-76433573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569559323	chr15:76433578-76433579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76083741	chr15:76433580-76433581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79974355	chr15:76433581-76433582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34149031	chr15:76433594-76433595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150759830	chr15:76433615-76433616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182764370	chr15:76433616-76433617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576256264	chr15:76433662-76433663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139159818	chr15:76433697-76433698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185188357	chr15:76433721-76433722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144132881	chr15:76433738-76433739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564199687	chr15:76433744-76433745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs60470953	chr15:76433776-76433777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs57865215	chr15:76433782-76433783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541358402	chr15:76433789-76433790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56864609	chr15:76433799-76433800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61282503	chr15:76433800-76433801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146041383	chr15:76433805-76433806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372322175	chr15:76433859-76433860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546315492	chr15:76433860-76433861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139488927	chr15:76433866-76433867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114766807	chr15:76433879-76433880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377161065	chr15:76433898-76433899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144233629	chr15:76433901-76433902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545985699	chr15:76433903-76433904	Weak transcription	n/a	n/a	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:1533 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

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	chr15:76431000-76433000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:76431600-76433000	Enhancers	H1 Cell Line	embryonic stem cell
5	chr15:76431600-76433000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr15:76431800-76433000	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr15:76431800-76433200	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr15:76432000-76433000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr15:76432000-76433000	Enhancers	Colon Smooth Muscle	Colon
10	chr15:76432000-76433000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr15:76432000-76433000	Enhancers	Left Ventricle	heart
12	chr15:76432000-76433000	Bivalent Enhancer	Stomach Mucosa	stomach
13	chr15:76432000-76433000	Enhancers	NHEK	skin
14	chr15:76432200-76433000	Enhancers	Brain Substantia Nigra	brain
15	chr15:76432200-76433600	Enhancers	Spleen	Spleen
16	chr15:76432400-76433000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr15:76432400-76433000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr15:76432400-76433200	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr15:76432400-76434000	Weak transcription	Fetal Heart	heart
20	chr15:76432400-76440400	Weak transcription	Pancreas	Pancrea
21	chr15:76432400-76442800	Weak transcription	Gastric	stomach
22	chr15:76432600-76433000	Enhancers	Right Atrium	heart
23	chr15:76432600-76433200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr15:76432600-76440400	Weak transcription	Placenta	Placenta
25	chr15:76432600-76442800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr15:76432800-76433000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr15:76432800-76433000	Enhancers	Adipose Nuclei	Adipose
28	chr15:76432800-76433000	Enhancers	Colonic Mucosa	Colon
29	chr15:76432800-76433000	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr15:76432800-76433000	Enhancers	HUVEC	blood vessel
31	chr15:76432800-76433000	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr15:76432800-76433000	Flanking Active TSS	Osteobl	bone
33	chr15:76432800-76433600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr15:76433000-76436600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr15:76433000-76437000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr15:76433000-76437400	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr15:76433000-76439600	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr15:76433000-76440400	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr15:76433000-76442800	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr15:76433000-76452800	Weak transcription	Right Atrium	heart
41	chr15:76433200-76440600	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr15:76433600-76439800	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr15:76433600-76440400	Weak transcription	Spleen	Spleen
44	chr15:76434000-76434200	Enhancers	Fetal Heart	heart
45	chr15:76434200-76435000	Weak transcription	Fetal Heart	heart
46	chr15:76435000-76435400	Enhancers	Fetal Heart	heart
47	chr15:76435400-76435800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr15:76436600-76438200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr15:76436800-76438400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr15:76437000-76437200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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