Variant report

Variant	esv15501
Chromosome Location	chr15:52265256-52273371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr15:52265123-52265666	MCF-7	breast:	n/a	n/a
2	CEBPB	chr15:52271916-52271942	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr15:52265140-52265635	MCF-7	breast:	n/a	n/a
4	CEBPB	chr15:52265280-52265573	HepG2	liver:	n/a	n/a
5	CEBPB	chr15:52271910-52271954	K562	blood:	n/a	chr15:52271941-52271952
6	CEBPB	chr15:52271930-52271958	HepG2	liver:	n/a	chr15:52271941-52271952
7	CTCF	chr15:52265579-52265676	MCF-7	breast:	n/a	n/a
8	CTCF	chr15:52265586-52265648	MCF-7	breast:	n/a	n/a
9	CTCF	chr15:52265560-52265710	GM12874	blood:	n/a	n/a
10	FOS	chr15:52265721-52265726	MCF10A-Er-Src	breast:	n/a	n/a
11	JUND	chr15:52265623-52265847	HepG2	liver:	n/a	chr15:52265736-52265746 chr15:52265735-52265746 chr15:52265737-52265746 chr15:52265736-52265745 chr15:52265734-52265742
12	MAFF	chr15:52266042-52266313	HepG2	liver:	n/a	chr15:52266161-52266179
13	MAFK	chr15:52266035-52266347	HepG2	liver:	n/a	chr15:52266163-52266178 chr15:52266163-52266174
14	MAFK	chr15:52266067-52266267	HepG2	liver:	n/a	chr15:52266163-52266178 chr15:52266163-52266174
15	MAFK	chr15:52266059-52266320	IMR90	lung:	n/a	chr15:52266163-52266178 chr15:52266163-52266174
16	POLR2A	chr15:52266417-52266434	K562	blood:	n/a	n/a
17	POLR2A	chr15:52269964-52269979	HepG2	liver:	n/a	n/a
18	POLR2A	chr15:52269947-52269959	HepG2	liver:	n/a	n/a
19	POLR2A	chr15:52269397-52269524	K562	blood:	n/a	n/a
20	STAT1	chr15:52267791-52268280	Hela-S3	cervix:	n/a	chr15:52268038-52268049

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:52267193-52267243	GM12891	blood:	n/a
2	chr15:52267193-52267243	AG04450	lung:	fetal
3	chr15:52267193-52267243	HIPEpiC	eye:	n/a
4	chr15:52267193-52267243	NHDF-neo	bronchial:	n/a
5	chr15:52267193-52267243	K562	blood:	n/a
6	chr15:52267193-52267243	GM19239	blood:	n/a
7	chr15:52267193-52267243	PANC-1	pancreas:	n/a
8	chr15:52267193-52267243	HPAEpiC	pulmonary alveolar:	n/a
9	chr15:52267193-52267243	HRE	kidney:	n/a
10	chr15:52267193-52267243	HCF	heart:	n/a
11	chr15:52267193-52267243	IMR90	lung:	fetal
12	chr15:52267193-52267243	T-47D	breast:	n/a
13	chr15:52267193-52267243	HEK293	kidney:	embryo
14	chr15:52267193-52267243	HCPEpiC	choroid plexus:	n/a
15	chr15:52267193-52267243	HAEpiC	amniotic membrane:	n/a
16	chr15:52267193-52267243	NB4	blood:	n/a
17	chr15:52267193-52267243	HRCEpiC	kidney:	n/a
18	chr15:52267193-52267243	PrEC	prostate:	n/a
19	chr15:52267193-52267243	HEEpiC	esophagus:	n/a
20	chr15:52267193-52267243	HUVEC	blood vessel:	n/a
21	chr15:52267193-52267243	HRPEpiC	eye:	n/a
22	chr15:52267193-52267243	SK-N-SH_RA	brain:	n/a
23	chr15:52267193-52267243	GM12878	blood:	n/a
24	chr15:52267193-52267243	HepG2	liver:	n/a
25	chr15:52267193-52267243	ovcar-3	ovarian:	n/a
26	chr15:52267193-52267243	Jurkat	blood:	n/a
27	chr15:52267193-52267243	BJ	skin:	n/a
28	chr15:52267193-52267243	AG04449	skin:	fetal
29	chr15:52267193-52267243	ProgFib	skin:	n/a
30	chr15:52267193-52267243	SAEC	small airway:	n/a
31	chr15:52267193-52267243	HMEC	breast:	n/a
32	chr15:52267193-52267243	NHBE	bronchial:	n/a
33	chr15:52267193-52267243	Hela-S3	cervix:	n/a
34	chr15:52267193-52267243	NT2-D1	testis:	n/a
35	chr15:52267193-52267243	HCT-116	colon:	n/a
36	chr15:52267193-52267243	A549	lung:	n/a
37	chr15:52267193-52267243	SK-N-SH	brain:	n/a
38	chr15:52267193-52267243	AoSMC	blood vessel:	n/a
39	chr15:52267193-52267243	H1-hESC	embryonic stem cell:	embryo
40	chr15:52267193-52267243	HNPCEpiC	eye:	n/a
41	chr15:52267193-52267243	GM12892	blood:	n/a
42	chr15:52267193-52267243	ECC-1	luminal epithelium:	n/a
43	chr15:52267193-52267243	RPTEC	kidney:	n/a
44	chr15:52267193-52267243	Hepatocyte	liver:	n/a
45	chr15:52267193-52267243	Caco-2	colon:	n/a
46	chr15:52267193-52267243	NH-A	brain:	n/a
47	chr15:52267193-52267243	HL-60	blood:	n/a
48	chr15:52267193-52267243	AG09319	gingival:	n/a
49	chr15:52267193-52267243	MCF-7	breast:	n/a
50	chr15:52267193-52267243	HCM	heart:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:52267594..52270331-chr15:52272576..52274636,3	MCF-7	breast:
2	chr15:52264304..52267297-chr15:52410135..52412517,2	MCF-7	breast:
3	chr15:52267047..52268763-chr15:52371441..52374035,2	K562	blood:
4	chr15:52265430..52265936-chr15:52370586..52371262,2	K562	blood:
5	chr15:52269022..52271113-chr15:52277354..52279460,2	MCF-7	breast:
6	chr15:52262270..52265607-chr15:52309730..52314612,10	K562	blood:
7	chr15:52272236..52273812-chr15:52299761..52301744,2	K562	blood:
8	chr15:52261233..52265470-chr15:52469433..52474401,7	MCF-7	breast:
9	chr15:52267594..52270331-chr15:52272576..52274636,3	MCF-7	breast:
10	chr15:52272756..52275955-chr15:52369833..52372310,3	MCF-7	breast:
11	chr15:52272788..52276993-chr15:52369760..52371998,4	MCF-7	breast:
12	chr15:52272584..52276027-chr15:52308541..52312916,5	K562	blood:
13	chr15:52263208..52265625-chr15:52404085..52407650,4	MCF-7	breast:
14	chr15:52272443..52274627-chr15:52305698..52308304,2	K562	blood:
15	chr15:52262830..52265268-chr15:52372078..52374982,4	MCF-7	breast:
16	chr15:52262263..52265564-chr15:52309489..52315686,9	K562	blood:
17	chr15:52266921..52268436-chr15:52310388..52312798,2	MCF-7	breast:
18	chr15:52272323..52273861-chr15:52410160..52412706,2	MCF-7	breast:
19	chr15:52273097..52274841-chr15:52286884..52288398,2	K562	blood:
20	chr15:52269337..52272220-chr15:52273087..52274635,2	MCF-7	breast:
21	chr15:52273041..52275862-chr15:52300749..52303075,2	MCF-7	breast:
22	chr15:52243665..52246508-chr15:52262168..52265352,3	MCF-7	breast:
23	chr15:52244109..52249001-chr15:52262072..52265545,5	MCF-7	breast:
24	chr15:52272035..52276768-chr15:52309954..52313442,7	MCF-7	breast:
25	chr15:52262145..52266701-chr15:52309209..52314377,19	MCF-7	breast:
26	chr15:52266394..52269371-chr17:57935595..57937194,2	MCF-7	breast:
27	chr15:52271637..52274025-chr15:52275587..52277212,2	MCF-7	breast:
28	chr15:52073675..52076293-chr15:52262420..52265302,2	MCF-7	breast:
29	chr15:52273281..52276233-chr15:52432324..52433834,2	MCF-7	breast:
30	chr15:52268028..52270216-chr15:52470821..52473204,2	MCF-7	breast:
31	chr15:52271043..52273593-chr15:52500641..52502378,2	MCF-7	breast:
32	chr15:52262628..52265811-chr15:52469801..52473537,4	MCF-7	breast:
33	chr15:52259207..52267788-chr15:52308373..52314434,24	MCF-7	breast:
34	chr15:52272930..52275289-chr15:52472014..52473869,2	MCF-7	breast:
35	chr15:52271865..52274806-chr15:52313995..52316353,2	MCF-7	breast:
36	chr15:52264141..52265648-chr15:52426026..52428333,2	MCF-7	breast:
37	chr15:52269337..52272220-chr15:52273087..52274635,2	MCF-7	breast:

No data

Variant related genes	Relation type
LEO1	TF binding region
LEO1	CpG island
ENSG00000166477	chromatin interactions
ENSG00000259577	chromatin interactions
ENSG00000069966	chromatin interactions
ENSG00000137875	chromatin interactions
ENSG00000259178	chromatin interactions
ENSG00000069956	chromatin interactions
ENSG00000128872	chromatin interactions
ENSG00000259438	chromatin interactions

Extended variants
information (count: 337 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558455148	chr15:52265259-52265260	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs149573166	chr15:52265288-52265289	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs368739678	chr15:52265304-52265305	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs144140301	chr15:52265323-52265324	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs386783961	chr15:52265332-52265333	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs189181841	chr15:52265334-52265335	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs558824118	chr15:52265348-52265349	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs541910870	chr15:52265362-52265363	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs16964653	chr15:52265415-52265416	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs568665260	chr15:52265425-52265426	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs553485619	chr15:52265446-52265447	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs531983356	chr15:52265453-52265454	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs117221424	chr15:52265455-52265456	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs144389411	chr15:52265477-52265478	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs147814639	chr15:52265491-52265492	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs371377422	chr15:52265592-52265593	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs3110553	chr15:52265600-52265601	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs529997617	chr15:52265682-52265683	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs539154055	chr15:52265724-52265725	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs139685888	chr15:52265747-52265748	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs569797572	chr15:52265758-52265759	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs558746900	chr15:52265813-52265814	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs536873236	chr15:52265857-52265858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs145091056	chr15:52265944-52265945	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111354868	chr15:52265959-52265960	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs180705789	chr15:52265998-52265999	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs185754849	chr15:52265999-52266000	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs140708012	chr15:52266010-52266011	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs550647696	chr15:52266013-52266014	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2254294	chr15:52266075-52266076	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs574226226	chr15:52266138-52266139	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs150096041	chr15:52266173-52266174	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs367827635	chr15:52266182-52266183	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs79993337	chr15:52266264-52266265	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs575390075	chr15:52266337-52266338	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs544493151	chr15:52266368-52266369	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs545886918	chr15:52266479-52266480	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565495551	chr15:52266491-52266492	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145174472	chr15:52266574-52266575	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs541716753	chr15:52266576-52266577	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559793909	chr15:52266578-52266579	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs188557949	chr15:52266580-52266581	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs36038468	chr15:52266584-52266585	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs181174105	chr15:52266589-52266590	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs569683440	chr15:52266592-52266593	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs371637026	chr15:52266594-52266595	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs186239900	chr15:52266619-52266620	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs138917982	chr15:52266630-52266631	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376914136	chr15:52266639-52266640	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs534513144	chr15:52266676-52266677	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52264000-52265400	Active TSS	HepG2	liver
2	chr15:52264600-52265600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:52264600-52265600	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr15:52264600-52265800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr15:52264600-52266000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr15:52264600-52266000	Enhancers	Placenta	Placenta
7	chr15:52264600-52266400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr15:52264600-52273000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr15:52264600-52273000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr15:52264600-52273000	Weak transcription	Liver	Liver
11	chr15:52264600-52273000	Weak transcription	Right Ventricle	heart
12	chr15:52264600-52273600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr15:52264600-52273600	Weak transcription	Brain Hippocampus Middle	brain
14	chr15:52264600-52273600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr15:52264600-52273600	Weak transcription	Stomach Mucosa	stomach
16	chr15:52264600-52273800	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr15:52264600-52273800	Weak transcription	Brain Anterior Caudate	brain
18	chr15:52264600-52273800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr15:52264600-52273800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr15:52264600-52273800	Weak transcription	Brain Substantia Nigra	brain
21	chr15:52264600-52273800	Weak transcription	Thymus	Thymus
22	chr15:52264600-52274000	Weak transcription	Colonic Mucosa	Colon
23	chr15:52264600-52274200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr15:52264600-52274400	Weak transcription	Pancreas	Pancrea
25	chr15:52264800-52265400	Weak transcription	HUVEC	blood vessel
26	chr15:52264800-52265600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr15:52264800-52265600	Enhancers	Dnd41	blood
28	chr15:52264800-52266600	Weak transcription	Brain Germinal Matrix	brain
29	chr15:52264800-52269600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr15:52264800-52273000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr15:52264800-52273000	Weak transcription	Hela-S3	cervix
32	chr15:52264800-52273200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr15:52264800-52273200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr15:52264800-52273600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr15:52264800-52273600	Weak transcription	NHEK	skin
36	chr15:52264800-52273800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr15:52264800-52273800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr15:52264800-52273800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr15:52264800-52273800	Weak transcription	Fetal Muscle Leg	muscle
40	chr15:52264800-52274000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr15:52264800-52274000	Weak transcription	Fetal Intestine Large	intestine
42	chr15:52265000-52265400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr15:52265000-52266000	Weak transcription	Fetal Muscle Trunk	muscle
44	chr15:52265000-52267200	Weak transcription	Fetal Stomach	stomach
45	chr15:52265000-52273000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:52265000-52273800	Weak transcription	HSMM	muscle
47	chr15:52265200-52265400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:52265200-52265400	Flanking Active TSS	Placenta Amnion	Placenta Amnion
49	chr15:52265200-52265800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr15:52265200-52265800	Weak transcription	Fetal Intestine Small	intestine

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