Variant report

Variant	nsv1053775
Chromosome Location	chr15:76460462-76485966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:895)
CpG islands
(count:795)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	chr15:76478041-76478258	HepG2	liver:	n/a	n/a
3	ATF2	chr15:76473954-76474425	GM12878	blood:	n/a	n/a
4	ATF2	chr15:76483089-76483813	GM12878	blood:	n/a	n/a
5	ATF2	chr15:76473823-76474454	GM12878	blood:	n/a	n/a
6	ATF3	chr15:76461359-76461682	GM12878	blood:	n/a	n/a
7	ATF3	chr15:76461375-76461737	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr15:76461499-76461617	GM12878	blood:	n/a	n/a
9	ATF3	chr15:76461421-76461690	K562	blood:	n/a	n/a
10	BACH1	chr15:76483297-76483365	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr15:76473865-76474455	GM12878	blood:	n/a	chr15:76474119-76474130
12	BATF	chr15:76473923-76474319	GM12878	blood:	n/a	chr15:76474119-76474130
13	BCL11A	chr15:76474032-76474320	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:76473914-76474363	GM12878	blood:	n/a	n/a
15	BCL3	chr15:76482892-76483810	A549	lung:	n/a	n/a
16	BCLAF1	chr15:76473788-76474517	GM12878	blood:	n/a	n/a
17	BCLAF1	chr15:76473905-76474445	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:76469949-76470149	A549	lung:	n/a	n/a
19	BHLHE40	chr15:76483122-76483431	K562	blood:	n/a	n/a
20	BHLHE40	chr15:76473924-76474330	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:76472787-76472910	K562	blood:	n/a	n/a
22	BHLHE40	chr15:76472876-76472910	HepG2	liver:	n/a	n/a
23	BHLHE40	chr15:76482536-76482865	K562	blood:	n/a	n/a
24	BHLHE40	chr15:76483088-76483437	GM12878	blood:	n/a	n/a
25	BRCA1	chr15:76483097-76483525	Hela-S3	cervix:	n/a	chr15:76483441-76483448
26	BRCA1	chr15:76483134-76483378	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr15:76483167-76483490	HepG2	liver:	n/a	chr15:76483441-76483448
28	CBX3	chr15:76477995-76478351	K562	blood:	n/a	n/a
29	CEBPB	chr15:76470103-76470357	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:76469800-76470434	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr15:76475123-76475449	IMR90	lung:	n/a	n/a
32	CEBPB	chr15:76470072-76470377	A549	lung:	n/a	n/a
33	CEBPB	chr15:76470121-76470486	HepG2	liver:	n/a	n/a
34	CEBPB	chr15:76482808-76483429	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr15:76482803-76483407	MCF-7	breast:	n/a	n/a
36	CEBPB	chr15:76482949-76483412	Hela-S3	cervix:	n/a	n/a
37	CHD1	chr15:76474037-76474475	GM12878	blood:	n/a	n/a
38	CHD2	chr15:76469943-76470221	HepG2	liver:	n/a	n/a
39	CHD2	chr15:76473975-76474412	GM12878	blood:	n/a	n/a
40	CHD2	chr15:76483093-76483441	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr15:76483147-76483430	K562	blood:	n/a	n/a
42	CHD2	chr15:76483160-76483398	HepG2	liver:	n/a	n/a
43	CHD2	chr15:76483082-76483493	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr15:76469883-76470465	Hela-S3	cervix:	n/a	n/a
45	CREB1	chr15:76473855-76474574	GM12878	blood:	n/a	n/a
46	CREB1	chr15:76470047-76470380	A549	lung:	n/a	n/a
47	CTCF	chr15:76483700-76483850	GM12874	blood:	n/a	chr15:76483801-76483814
48	CTCF	chr15:76483180-76483330	GM12866	blood:	n/a	chr15:76483268-76483284 chr15:76483269-76483290 chr15:76483271-76483278 chr15:76483267-76483285 chr15:76483318-76483326
49	CTCF	chr15:76477880-76478170	A549	lung:	n/a	n/a
50	CTCF	chr15:76478120-76478270	HUVEC	blood vessel:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76470979-76471029	NH-A	brain:	n/a
2	chr15:76483201-76483251	HepG2	liver:	n/a
3	chr15:76470979-76471029	NH-A	brain:	n/a
4	chr15:76483201-76483251	HepG2	liver:	n/a
5	chr15:76483201-76483251	NHBE	bronchial:	n/a
6	chr15:76483344-76483394	HRE	kidney:	n/a
7	chr15:76478102-76478152	SK-N-MC	brain:	n/a
8	chr15:76484625-76484675	ovcar-3	ovarian:	n/a
9	chr15:76483201-76483251	SK-N-MC	brain:	n/a
10	chr15:76483344-76483394	NB4	blood:	n/a
11	chr15:76480434-76480484	ovcar-3	ovarian:	n/a
12	chr15:76484625-76484675	RPTEC	kidney:	n/a
13	chr15:76484379-76484429	Jurkat	blood:	n/a
14	chr15:76470979-76471029	ECC-1	luminal epithelium:	n/a
15	chr15:76478102-76478152	U87	brain:	n/a
16	chr15:76480434-76480484	T-47D	breast:	n/a
17	chr15:76470979-76471029	HepG2	liver:	n/a
18	chr15:76484625-76484675	AG09309	skin:	n/a
19	chr15:76483201-76483251	HCF	heart:	n/a
20	chr15:76484102-76484152	PFSK-1	brain:	n/a
21	chr15:76461960-76462010	HMEC	breast:	n/a
22	chr15:76462821-76462871	HL-60	blood:	n/a
23	chr15:76461960-76462010	GM12878	blood:	n/a
24	chr15:76484625-76484675	SKMC	muscle:	n/a
25	chr15:76478102-76478152	NH-A	brain:	n/a
26	chr15:76483344-76483394	PrEC	prostate:	n/a
27	chr15:76484473-76484523	HL-60	blood:	n/a
28	chr15:76475969-76476019	HRPEpiC	eye:	n/a
29	chr15:76484473-76484523	HEK293	kidney:	embryo
30	chr15:76470979-76471029	MCF-7	breast:	n/a
31	chr15:76462821-76462871	HCT-116	colon:	n/a
32	chr15:76483281-76483331	NH-A	brain:	n/a
33	chr15:76483201-76483251	ovcar-3	ovarian:	n/a
34	chr15:76483344-76483394	MCF10A-Er-Src	breast:	n/a
35	chr15:76478102-76478152	IMR90	lung:	fetal
36	chr15:76484379-76484429	HCM	heart:	n/a
37	chr15:76478102-76478152	HEEpiC	esophagus:	n/a
38	chr15:76470979-76471029	GM06990	blood:	n/a
39	chr15:76484473-76484523	BE2_C	brain:	n/a
40	chr15:76483281-76483331	BJ	skin:	n/a
41	chr15:76470979-76471029	HCPEpiC	choroid plexus:	n/a
42	chr15:76484473-76484523	Hepatocyte	liver:	n/a
43	chr15:76480434-76480484	RPTEC	kidney:	n/a
44	chr15:76484625-76484675	H1-hESC	embryonic stem cell:	embryo
45	chr15:76470979-76471029	HIPEpiC	eye:	n/a
46	chr15:76462821-76462871	HAEpiC	amniotic membrane:	n/a
47	chr15:76483281-76483331	GM12891	blood:	n/a
48	chr15:76478102-76478152	SK-N-SH	brain:	n/a
49	chr15:76461960-76462010	SAEC	small airway:	n/a
50	chr15:76480434-76480484	H1-hESC	embryonic stem cell:	embryo

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76483023..76483731-chr15:76527305..76528242,4	MCF-7	breast:
2	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
3	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
4	chr15:76481529..76484202-chr15:76633877..76636476,2	K562	blood:
5	chr15:76484853..76487491-chr15:76488798..76492049,5	K562	blood:
6	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
7	chr15:76482846..76483696-chr15:76577399..76578194,4	MCF-7	breast:
8	chr15:76453204..76454747-chr15:76459797..76461438,2	MCF-7	breast:
9	chr15:76482840..76483720-chr15:77132911..77133894,4	MCF-7	breast:
10	chr15:76482820..76483740-chr15:76577311..76578273,3	K562	blood:
11	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
12	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
13	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
14	chr15:76482420..76485297-chr15:76485451..76488299,2	K562	blood:
15	chr15:76482829..76483665-chr15:77158796..77159907,4	MCF-7	breast:
16	chr15:76478149..76479732-chr15:76481760..76484387,3	K562	blood:
17	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
18	chr15:76482689..76486583-chr15:76628039..76631365,3	K562	blood:
19	chr15:76461088..76462629-chr15:76483253..76485151,2	K562	blood:
20	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
21	chr15:76482740..76483457-chr15:76626133..76626814,2	MCF-7	breast:
22	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
23	chr15:76482924..76483751-chr15:76625816..76626899,5	MCF-7	breast:
24	chr15:76484065..76486868-chr15:76602060..76604082,2	MCF-7	breast:
25	chr15:76478115..76478633-chr15:76622409..76623267,2	MCF-7	breast:
26	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
27	chr15:76457780..76460448-chr15:76461142..76462656,2	K562	blood:
28	chr15:76477747..76478594-chr15:76625784..76626375,2	MCF-7	breast:
29	chr15:76452837..76455028-chr15:76460465..76463193,2	K562	blood:
30	chr15:76483246..76483790-chr15:77158830..77159724,2	K562	blood:
31	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
32	chr15:76482702..76486394-chr15:76633656..76636389,3	K562	blood:
33	chr15:76483018..76483722-chr15:76622624..76623279,3	K562	blood:
34	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
35	chr15:76478027..76479862-chr15:76483019..76485634,3	MCF-7	breast:
36	chr15:76483216..76483808-chr15:76625887..76626857,3	K562	blood:

No data

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

Extended variants
information (count: 1043 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1043 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531105035	chr15:76460478-76460479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563903921	chr15:76460535-76460536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528049844	chr15:76460557-76460558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs28446264	chr15:76460576-76460577	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs567774689	chr15:76460617-76460618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529058621	chr15:76460677-76460678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551006066	chr15:76460721-76460722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115018140	chr15:76460761-76460762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571195776	chr15:76460784-76460785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569174079	chr15:76460813-76460814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373461847	chr15:76460832-76460833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs58863068	chr15:76460845-76460846	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558941325	chr15:76460862-76460863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570883540	chr15:76460904-76460905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534983846	chr15:76460916-76460917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189959809	chr15:76460945-76460946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs62030164	chr15:76460989-76460990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181353747	chr15:76460991-76460992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185952501	chr15:76461018-76461019	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373792991	chr15:76461095-76461096	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs190824441	chr15:76461103-76461104	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs386785479	chr15:76461179-76461180	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs74024098	chr15:76461180-76461181	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs564767291	chr15:76461222-76461223	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201783584	chr15:76461234-76461235	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78579784	chr15:76461245-76461246	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs28647796	chr15:76461263-76461264	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs139682243	chr15:76461299-76461300	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs142677034	chr15:76461328-76461329	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs151017816	chr15:76461340-76461341	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs72736833	chr15:76461397-76461398	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs533124258	chr15:76461442-76461443	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs116936895	chr15:76461480-76461481	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181736732	chr15:76461494-76461495	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149994183	chr15:76461526-76461527	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553391544	chr15:76461533-76461534	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145199630	chr15:76461544-76461545	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs75361446	chr15:76461559-76461560	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs57906605	chr15:76461576-76461577	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs575764254	chr15:76461654-76461655	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77476788	chr15:76461656-76461657	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145062708	chr15:76461681-76461682	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186452798	chr15:76461683-76461684	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138950400	chr15:76461766-76461767	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570144097	chr15:76461819-76461820	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2959857	chr15:76461848-76461849	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs150798816	chr15:76461849-76461850	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs72736834	chr15:76461872-76461873	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543999775	chr15:76461904-76461905	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562572108	chr15:76461924-76461925	Enhancers Weak transcription Genic enhancers	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:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76443200-76483000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr15:76443400-76466000	Weak transcription	Brain Angular Gyrus	brain
3	chr15:76453400-76461000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr15:76454600-76461000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:76455600-76463000	Weak transcription	Colon Smooth Muscle	Colon
6	chr15:76455800-76465200	Weak transcription	Right Atrium	heart
7	chr15:76456000-76461000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr15:76456200-76461000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr15:76456200-76462600	Weak transcription	Stomach Smooth Muscle	stomach
10	chr15:76456200-76465400	Weak transcription	Fetal Intestine Small	intestine
11	chr15:76456400-76460800	Weak transcription	NHDF-Ad	bronchial
12	chr15:76456400-76461000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr15:76456400-76461000	Weak transcription	Lung	lung
14	chr15:76456600-76461000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:76456600-76461000	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr15:76456600-76461000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr15:76456600-76461200	Weak transcription	Hela-S3	cervix
18	chr15:76456600-76462000	Weak transcription	NHLF	lung
19	chr15:76457400-76462000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr15:76457600-76460600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:76457600-76461800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr15:76457600-76462600	Weak transcription	Spleen	Spleen
23	chr15:76457800-76461000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr15:76458800-76461000	Weak transcription	Placenta	Placenta
25	chr15:76458800-76467600	Weak transcription	Pancreas	Pancrea
26	chr15:76459000-76460600	Weak transcription	Fetal Stomach	stomach
27	chr15:76459000-76463800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr15:76459000-76465400	Weak transcription	Ovary	ovary
29	chr15:76460200-76461200	Enhancers	Fetal Muscle Leg	muscle
30	chr15:76460200-76463200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:76460200-76463200	Enhancers	HSMM	muscle
32	chr15:76460200-76463600	Enhancers	HSMMtube	muscle
33	chr15:76460600-76461000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr15:76460600-76461400	Enhancers	Fetal Muscle Trunk	muscle
35	chr15:76460600-76463400	Enhancers	Fetal Stomach	stomach
36	chr15:76460800-76463000	Enhancers	NHDF-Ad	bronchial
37	chr15:76461000-76461200	Enhancers	Esophagus	oesophagus
38	chr15:76461000-76461200	Enhancers	Lung	lung
39	chr15:76461000-76461400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr15:76461000-76461400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr15:76461000-76461400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr15:76461000-76461400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr15:76461000-76461400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr15:76461000-76461400	Enhancers	K562	blood
45	chr15:76461000-76461600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr15:76461000-76461600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr15:76461000-76462000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr15:76461000-76462000	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr15:76461000-76462800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr15:76461000-76463200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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