Variant report

Variant	esv18367
Chromosome Location	chr15:83327137-83332372
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	BHLHE40	chr15:83331935-83332230	HepG2	liver:	n/a	n/a
2	BHLHE40	chr15:83331916-83332262	K562	blood:	n/a	n/a
3	CBX3	chr15:83331797-83332283	K562	blood:	n/a	n/a
4	CBX3	chr15:83331916-83332226	K562	blood:	n/a	n/a
5	CEBPB	chr15:83331262-83331301	HepG2	liver:	n/a	chr15:83331279-83331290
6	CEBPB	chr15:83331286-83331311	A549	lung:	n/a	n/a
7	CHD2	chr15:83331947-83332175	K562	blood:	n/a	n/a
8	E2F6	chr15:83331939-83332382	K562	blood:	n/a	n/a
9	E2F6	chr15:83331747-83332322	K562	blood:	n/a	n/a
10	E2F6	chr15:83331780-83332468	H1-hESC	embryonic stem cell:	n/a	n/a
11	E2F6	chr15:83331845-83332378	H1-hESC	embryonic stem cell:	n/a	n/a
12	E2F6	chr15:83331893-83332350	K562	blood:	n/a	n/a
13	EGR1	chr15:83331970-83332187	K562	blood:	n/a	n/a
14	ETS1	chr15:83331969-83332123	K562	blood:	n/a	n/a
15	GTF2F1	chr15:83331957-83332169	H1-hESC	embryonic stem cell:	n/a	n/a
16	HCFC1	chr15:83331899-83332276	K562	blood:	n/a	n/a
17	HCFC1	chr15:83331814-83332364	Hela-S3	cervix:	n/a	n/a
18	HNF4G	chr15:83331979-83332133	HepG2	liver:	n/a	n/a
19	JUND	chr15:83331937-83332252	K562	blood:	n/a	n/a
20	MAFK	chr15:83332032-83332069	HepG2	liver:	n/a	n/a
21	MAFK	chr15:83332044-83332193	K562	blood:	n/a	n/a
22	MAX	chr15:83331898-83332275	K562	blood:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
23	MAX	chr15:83331802-83332363	HepG2	liver:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
24	MAX	chr15:83331921-83332332	HCT-116	colon:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
25	MAX	chr15:83331825-83332400	ECC-1	luminal epithelium:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
26	MAX	chr15:83331847-83332289	HepG2	liver:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
27	MAX	chr15:83331837-83332425	A549	lung:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
28	MAX	chr15:83331846-83332224	K562	blood:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
29	MAX	chr15:83331885-83332237	SK-N-SH	brain:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
30	MAX	chr15:83331885-83332284	SK-N-SH	brain:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
31	MAX	chr15:83331899-83332312	H1-hESC	embryonic stem cell:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
32	MAX	chr15:83331919-83332240	HepG2	liver:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
33	MAX	chr15:83331767-83332402	MCF-7	breast:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
34	MAX	chr15:83331930-83332262	A549	lung:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
35	MAX	chr15:83331801-83332381	MCF-7	breast:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
36	MAX	chr15:83331819-83332375	ECC-1	luminal epithelium:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
37	MAX	chr15:83331800-83332364	H1-hESC	embryonic stem cell:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
38	MAX	chr15:83331812-83332426	K562	blood:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
39	MAX	chr15:83331896-83332315	H1-hESC	embryonic stem cell:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
40	MAX	chr15:83331911-83332267	Hela-S3	cervix:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
41	MAX	chr15:83331879-83332302	NB4	blood:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
42	MAX	chr15:83331908-83332242	GM12878	blood:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
43	MAX	chr15:83331935-83332253	Hela-S3	cervix:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
44	MAX	chr15:83331814-83332367	HCT-116	colon:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
45	MAX	chr15:83331851-83332295	A549	lung:	n/a	chr15:83332090-83332099 chr15:83332088-83332098
46	MAZ	chr15:83331862-83332236	K562	blood:	n/a	chr15:83332090-83332099
47	MAZ	chr15:83332086-83332101	Hela-S3	cervix:	n/a	chr15:83332090-83332099
48	MXI1	chr15:83331900-83332641	IMR90	lung:	n/a	n/a
49	MXI1	chr15:83331959-83332232	GM12878	blood:	n/a	n/a
50	MXI1	chr15:83331951-83332235	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:83332065-83332115	SKMC	muscle:	n/a
2	chr15:83332065-83332115	SKMC	muscle:	n/a
3	chr15:83332087-83332137	HL-60	blood:	n/a
4	chr15:83331441-83331491	BJ	skin:	n/a
5	chr15:83332065-83332115	Caco-2	colon:	n/a
6	chr15:83331452-83331502	GM12878	blood:	n/a
7	chr15:83332087-83332137	PANC-1	pancreas:	n/a
8	chr15:83331452-83331502	HNPCEpiC	eye:	n/a
9	chr15:83331452-83331502	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:83332087-83332137	NT2-D1	testis:	n/a
11	chr15:83332087-83332137	CMK	blood:	n/a
12	chr15:83331586-83331636	GM06990	blood:	n/a
13	chr15:83331441-83331491	GM19239	blood:	n/a
14	chr15:83331452-83331502	NH-A	brain:	n/a
15	chr15:83332087-83332137	Caco-2	colon:	n/a
16	chr15:83331441-83331491	HRE	kidney:	n/a
17	chr15:83331441-83331491	ovcar-3	ovarian:	n/a
18	chr15:83331586-83331636	SK-N-MC	brain:	n/a
19	chr15:83331586-83331636	BJ	skin:	n/a
20	chr15:83332087-83332137	NB4	blood:	n/a
21	chr15:83332087-83332137	Jurkat	blood:	n/a
22	chr15:83332087-83332137	AoSMC	blood vessel:	n/a
23	chr15:83332087-83332137	HCM	heart:	n/a
24	chr15:83331452-83331502	NT2-D1	testis:	n/a
25	chr15:83332065-83332115	Jurkat	blood:	n/a
26	chr15:83332065-83332115	HRCEpiC	kidney:	n/a
27	chr15:83331586-83331636	HIPEpiC	eye:	n/a
28	chr15:83331441-83331491	AoSMC	blood vessel:	n/a
29	chr15:83331441-83331491	NH-A	brain:	n/a
30	chr15:83331441-83331491	HCPEpiC	choroid plexus:	n/a
31	chr15:83332065-83332115	GM06990	blood:	n/a
32	chr15:83331452-83331502	A549	lung:	n/a
33	chr15:83331586-83331636	ProgFib	skin:	n/a
34	chr15:83331452-83331502	Jurkat	blood:	n/a
35	chr15:83332065-83332115	K562	blood:	n/a
36	chr15:83331586-83331636	AG04450	lung:	fetal
37	chr15:83331452-83331502	LNCaP	prostate:	n/a
38	chr15:83331441-83331491	HCM	heart:	n/a
39	chr15:83332065-83332115	LNCaP	prostate:	n/a
40	chr15:83332087-83332137	HPAEpiC	pulmonary alveolar:	n/a
41	chr15:83331452-83331502	AG09309	skin:	n/a
42	chr15:83331586-83331636	PFSK-1	brain:	n/a
43	chr15:83332065-83332115	HepG2	liver:	n/a
44	chr15:83332087-83332137	AG04450	lung:	fetal
45	chr15:83331441-83331491	U87	brain:	n/a
46	chr15:83331441-83331491	HMEC	breast:	n/a
47	chr15:83332065-83332115	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:83332087-83332137	SK-N-MC	brain:	n/a
49	chr15:83332065-83332115	AG04449	skin:	fetal
50	chr15:83331452-83331502	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:83330156..83333342-chr15:83346386..83350515,4	MCF-7	breast:
2	chr15:83325295..83330219-chr15:83330483..83333738,7	K562	blood:
3	chr15:83326624..83328865-chr15:83351824..83354482,2	K562	blood:
4	chr15:83328672..83331748-chr15:83346249..83349279,3	MCF-7	breast:
5	chr15:83329409..83331309-chr15:83337250..83339534,2	K562	blood:
6	chr15:83327589..83329716-chr15:83417806..83419579,2	MCF-7	breast:
7	chr15:83330561..83333118-chr15:83349292..83351934,2	K562	blood:
8	chr15:83319337..83321947-chr15:83328368..83329898,2	K562	blood:
9	chr15:83321977..83323621-chr15:83325301..83327966,2	K562	blood:
10	chr15:83325295..83328709-chr15:83330365..83332547,4	K562	blood:
11	chr15:83311482..83314245-chr15:83326104..83328950,2	K562	blood:
12	chr15:83315603..83319675-chr15:83327659..83331605,4	K562	blood:

Variant related genes	Relation type
AP3B2	TF binding region
AP3B2	CpG island
ENSG00000259462	chromatin interactions
ENSG00000214575	chromatin interactions
ENSG00000103723	chromatin interactions
ENSG00000250988	chromatin interactions

Extended variants
information (count: 220 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:220 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117846384	chr15:83327192-83327193	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs35821061	chr15:83327244-83327245	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541424681	chr15:83327246-83327247	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs193109295	chr15:83327273-83327274	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182667103	chr15:83327278-83327279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs530951832	chr15:83327301-83327302	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187665273	chr15:83327305-83327306	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs145600636	chr15:83327317-83327318	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs372886632	chr15:83327341-83327342	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564048582	chr15:83327365-83327366	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs151089796	chr15:83327375-83327376	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs546537933	chr15:83327403-83327404	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140779683	chr15:83327412-83327413	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs376410811	chr15:83327449-83327450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs560463234	chr15:83327468-83327469	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371210423	chr15:83327522-83327523	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150104200	chr15:83327526-83327527	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565224687	chr15:83327539-83327540	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145471535	chr15:83327565-83327566	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs140248670	chr15:83327571-83327572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562493394	chr15:83327580-83327581	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551023844	chr15:83327594-83327595	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs529795718	chr15:83327650-83327651	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs145220340	chr15:83327670-83327671	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs138160791	chr15:83327700-83327701	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs527810610	chr15:83327701-83327702	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs114699687	chr15:83327775-83327776	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs370668602	chr15:83327803-83327804	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs192869158	chr15:83327811-83327812	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs184110907	chr15:83327812-83327813	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs142661481	chr15:83327840-83327841	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs144779566	chr15:83327887-83327888	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs148235606	chr15:83327912-83327913	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs557817223	chr15:83327955-83327956	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs12905138	chr15:83327999-83328000	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs141900450	chr15:83328006-83328007	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs560339640	chr15:83328008-83328009	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs77082021	chr15:83328086-83328087	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs549163579	chr15:83328152-83328153	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs542906859	chr15:83328208-83328209	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs562790793	chr15:83328218-83328219	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs551931229	chr15:83328231-83328232	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs150634084	chr15:83328294-83328295	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs570447805	chr15:83328316-83328317	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs201428733	chr15:83328319-83328320	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs188892600	chr15:83328325-83328326	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs201769141	chr15:83328344-83328345	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs533225118	chr15:83328345-83328346	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs367638774	chr15:83328354-83328355	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs540715932	chr15:83328372-83328373	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
abnormal development	18461090	CNVD
Intellectual disability	22102821	CNVD
renal disease	17924346	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:83317200-83331800	Weak transcription	Gastric	stomach
2	chr15:83317200-83336200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr15:83317600-83327800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr15:83319200-83327600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr15:83319200-83328200	Weak transcription	Brain Angular Gyrus	brain
6	chr15:83319200-83330400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr15:83319600-83327600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr15:83320200-83327800	Weak transcription	Brain Substantia Nigra	brain
9	chr15:83323000-83327600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr15:83324800-83331400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr15:83325200-83327600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr15:83325800-83333800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:83326200-83328800	Strong transcription	Fetal Brain Female	brain
14	chr15:83326400-83328200	Strong transcription	Brain Anterior Caudate	brain
15	chr15:83326600-83330400	Weak transcription	Fetal Brain Male	brain
16	chr15:83326600-83336000	Strong transcription	Brain Germinal Matrix	brain
17	chr15:83327000-83328800	Strong transcription	Brain Hippocampus Middle	brain
18	chr15:83327600-83328400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:83327600-83328600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr15:83327600-83328800	Strong transcription	Brain Cingulate Gyrus	brain
21	chr15:83327600-83331000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr15:83327800-83328800	Strong transcription	Brain Substantia Nigra	brain
23	chr15:83327800-83337400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr15:83328200-83328600	Strong transcription	Brain Angular Gyrus	brain
25	chr15:83328200-83331800	Weak transcription	Brain Anterior Caudate	brain
26	chr15:83328400-83329000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr15:83328600-83328800	Genic enhancers	Brain Angular Gyrus	brain
28	chr15:83328600-83330400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr15:83328800-83330400	Weak transcription	Brain Angular Gyrus	brain
30	chr15:83328800-83331200	Weak transcription	Brain Hippocampus Middle	brain
31	chr15:83328800-83331600	Weak transcription	Fetal Brain Female	brain
32	chr15:83328800-83332400	Weak transcription	Brain Cingulate Gyrus	brain
33	chr15:83328800-83342600	Weak transcription	Brain Substantia Nigra	brain
34	chr15:83329000-83329400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr15:83329400-83329600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr15:83329600-83329800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr15:83330400-83331000	Enhancers	Brain Angular Gyrus	brain
38	chr15:83330400-83331000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr15:83330400-83331400	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr15:83330400-83331400	Enhancers	Fetal Brain Male	brain
41	chr15:83330600-83331000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr15:83330800-83331000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr15:83331000-83331800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr15:83331000-83332200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr15:83331000-83332600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr15:83331000-83334200	Weak transcription	Brain Angular Gyrus	brain
47	chr15:83331200-83335200	Strong transcription	Brain Hippocampus Middle	brain
48	chr15:83331400-83331800	Genic enhancers	Brain Inferior Temporal Lobe	brain
49	chr15:83331400-83346600	Weak transcription	Fetal Brain Male	brain
50	chr15:83331600-83337800	Strong transcription	Fetal Brain Female	brain

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