Variant report

Variant	nsv94512
Chromosome Location	chr15:78794159-78801222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:507)
CpG islands
(count:610)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78799478-78800041	HepG2	liver:	n/a	n/a
2	BACH1	chr15:78799330-78799793	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr15:78799217-78800259	A549	lung:	n/a	chr15:78799561-78799569
4	BCL3	chr15:78799310-78800104	A549	lung:	n/a	chr15:78799561-78799569
5	BHLHE40	chr15:78799964-78800233	K562	blood:	n/a	n/a
6	BHLHE40	chr15:78799381-78799700	K562	blood:	n/a	n/a
7	BRCA1	chr15:78799567-78799949	Hela-S3	cervix:	n/a	chr15:78799762-78799769
8	BRCA1	chr15:78800227-78800266	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr15:78799221-78800154	K562	blood:	n/a	n/a
10	CCNT2	chr15:78799281-78800197	K562	blood:	n/a	n/a
11	CEBPB	chr15:78799571-78799773	K562	blood:	n/a	chr15:78799667-78799675
12	CEBPB	chr15:78799447-78799764	H1-hESC	embryonic stem cell:	n/a	chr15:78799667-78799675
13	CEBPB	chr15:78799544-78799926	HepG2	liver:	n/a	chr15:78799864-78799872 chr15:78799667-78799675
14	CEBPB	chr15:78797093-78797203	A549	lung:	n/a	n/a
15	CEBPB	chr15:78799471-78799960	Hela-S3	cervix:	n/a	chr15:78799864-78799872 chr15:78799667-78799675
16	CEBPZ	chr15:78799611-78799838	HepG2	liver:	n/a	n/a
17	CHD1	chr15:78800050-78800056	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr15:78799734-78800064	HepG2	liver:	n/a	n/a
19	CHD2	chr15:78799493-78800251	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr15:78799398-78800109	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr15:78800759-78800897	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr15:78799483-78800083	K562	blood:	n/a	n/a
23	CHD2	chr15:78799605-78800031	GM12878	blood:	n/a	n/a
24	CREB1	chr15:78799404-78800166	A549	lung:	n/a	n/a
25	CTCF	chr15:78799840-78799990	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr15:78799940-78800090	AG04449	skin:	n/a	n/a
27	CTCF	chr15:78800020-78800170	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr15:78799960-78800110	AG10803	skin:	n/a	n/a
29	CTCF	chr15:78799940-78800090	HMEC	breast:	n/a	n/a
30	CTCF	chr15:78799780-78799930	AG09319	gingival:	n/a	n/a
31	CTCF	chr15:78800260-78800410	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr15:78799880-78800030	SAEC	small airway:	n/a	n/a
33	CTCF	chr15:78799800-78799950	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr15:78799940-78800090	K562	blood:	n/a	n/a
35	CTCF	chr15:78799780-78799930	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr15:78799880-78800030	GM12866	blood:	n/a	n/a
37	CTCF	chr15:78799860-78800010	GM12864	blood:	n/a	n/a
38	CTCF	chr15:78800160-78800310	GM12878	blood:	n/a	n/a
39	CTCF	chr15:78799860-78800010	BE2_C	brain:	n/a	n/a
40	CTCF	chr15:78799960-78800110	GM12874	blood:	n/a	n/a
41	CTCF	chr15:78799863-78800017	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:78799900-78800050	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr15:78799900-78800076	Fibrobl	skin:	n/a	n/a
44	CTCF	chr15:78799940-78800090	GM12878	blood:	n/a	n/a
45	CTCF	chr15:78799780-78799930	HRE	kidney:	n/a	n/a
46	CTCF	chr15:78799969-78800039	GM10248	blood:	n/a	n/a
47	CTCF	chr15:78799892-78800079	GM19238	blood:	n/a	n/a
48	CTCF	chr15:78799860-78800010	GM12869	blood:	n/a	n/a
49	CTCF	chr15:78799900-78800050	GM12871	blood:	n/a	n/a
50	CTCF	chr15:78799820-78799970	GM12873	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78799689-78799739	GM12891	blood:	n/a
2	chr15:78799708-78799758	SK-N-SH_RA	brain:	n/a
3	chr15:78795944-78795994	NHBE	bronchial:	n/a
4	chr15:78800245-78800295	GM12878	blood:	n/a
5	chr15:78799708-78799758	MCF-7	breast:	n/a
6	chr15:78800245-78800295	SAEC	small airway:	n/a
7	chr15:78799792-78799842	PANC-1	pancreas:	n/a
8	chr15:78795944-78795994	HIPEpiC	eye:	n/a
9	chr15:78799507-78799557	GM19239	blood:	n/a
10	chr15:78799584-78799634	NHDF-neo	bronchial:	n/a
11	chr15:78799584-78799634	ProgFib	skin:	n/a
12	chr15:78800245-78800295	AG04449	skin:	fetal
13	chr15:78799806-78799856	NHDF-neo	bronchial:	n/a
14	chr15:78799806-78799856	HRPEpiC	eye:	n/a
15	chr15:78799812-78799862	SKMC	muscle:	n/a
16	chr15:78799812-78799862	LNCaP	prostate:	n/a
17	chr15:78799812-78799862	ProgFib	skin:	n/a
18	chr15:78799507-78799557	PrEC	prostate:	n/a
19	chr15:78799812-78799862	HCPEpiC	choroid plexus:	n/a
20	chr15:78799507-78799557	CMK	blood:	n/a
21	chr15:78799507-78799557	HCM	heart:	n/a
22	chr15:78799806-78799856	SK-N-MC	brain:	n/a
23	chr15:78799708-78799758	HCT-116	colon:	n/a
24	chr15:78799584-78799634	AG04449	skin:	fetal
25	chr15:78800245-78800295	HIPEpiC	eye:	n/a
26	chr15:78799689-78799739	GM19239	blood:	n/a
27	chr15:78800245-78800295	CMK	blood:	n/a
28	chr15:78799887-78799937	NHBE	bronchial:	n/a
29	chr15:78799507-78799557	NT2-D1	testis:	n/a
30	chr15:78800245-78800295	A549	lung:	n/a
31	chr15:78799507-78799557	AG09319	gingival:	n/a
32	chr15:78799792-78799842	GM12892	blood:	n/a
33	chr15:78799792-78799842	AG04449	skin:	fetal
34	chr15:78799792-78799842	A549	lung:	n/a
35	chr15:78799806-78799856	NHBE	bronchial:	n/a
36	chr15:78800245-78800295	Caco-2	colon:	n/a
37	chr15:78799806-78799856	GM12892	blood:	n/a
38	chr15:78799584-78799634	U87	brain:	n/a
39	chr15:78799507-78799557	Jurkat	blood:	n/a
40	chr15:78799708-78799758	NB4	blood:	n/a
41	chr15:78795944-78795994	AG04449	skin:	fetal
42	chr15:78799507-78799557	HepG2	liver:	n/a
43	chr15:78799792-78799842	AG09309	skin:	n/a
44	chr15:78799584-78799634	HEK293	kidney:	embryo
45	chr15:78799708-78799758	SKMC	muscle:	n/a
46	chr15:78800245-78800295	SK-N-SH	brain:	n/a
47	chr15:78799507-78799557	RPTEC	kidney:	n/a
48	chr15:78799812-78799862	HRCEpiC	kidney:	n/a
49	chr15:78799792-78799842	NB4	blood:	n/a
50	chr15:78799887-78799937	HL-60	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:78790366..78792147-chr15:78793354..78796412,3	K562	blood:
2	chr15:78800239..78802096-chr15:78806639..78809897,3	K562	blood:
3	chr15:78799175..78801434-chr15:78856957..78860049,3	K562	blood:
4	chr15:78798844..78801827-chr15:78830907..78834394,5	MCF-7	breast:
5	chr15:78798809..78800718-chr15:78830322..78833228,2	K562	blood:
6	chr15:78790204..78792403-chr15:78793483..78795992,2	MCF-7	breast:
7	chr15:78791381..78794333-chr15:78798862..78801849,3	MCF-7	breast:
8	chr15:78729311..78731587-chr15:78798062..78799852,2	K562	blood:
9	chr15:78800463..78801974-chr15:78805199..78807049,2	MCF-7	breast:
10	chr15:78799968..78802208-chr15:78803211..78805920,2	MCF-7	breast:
11	chr15:78791061..78794326-chr15:78831088..78834091,3	MCF-7	breast:
12	chr15:78785786..78788600-chr15:78798276..78800163,3	K562	blood:
13	chr15:78795126..78798276-chr15:78798396..78801540,3	K562	blood:
14	chr15:78798632..78802030-chr15:78802831..78805742,4	K562	blood:
15	chr15:78799834..78800344-chr19:17356570..17357495,2	Hela-S3	cervix:
16	chr15:78797464..78804546-chr15:78829529..78835433,12	MCF-7	breast:
17	chr15:78796921..78799074-chr15:78835568..78838304,2	K562	blood:
18	chr15:78791030..78793547-chr15:78800208..78802171,2	MCF-7	breast:
19	chr15:78798632..78801641-chr15:78802047..78805742,4	K562	blood:
20	chr15:78800242..78802455-chr15:78857304..78859272,2	MCF-7	breast:
21	chr15:78799623..78800208-chr3:169482291..169483011,2	Hela-S3	cervix:
22	chr15:78798595..78799352-chr17:47269636..47270545,2	HCT-116	colon:
23	chr15:78798048..78801609-chr15:78828919..78833228,5	K562	blood:

No data

Variant related genes	Relation type
HYKK	TF binding region
HYKK	CpG island
ENSG00000188266	chromatin interactions
ENSG00000136381	chromatin interactions
ENSG00000041357	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000169684	chromatin interactions
ENSG00000160113	chromatin interactions
ENSG00000268838	chromatin interactions

Extended variants
information (count: 276 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56318078	chr15:78794163-78794164	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs80211282	chr15:78794164-78794165	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371290316	chr15:78794165-78794166	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs551311198	chr15:78794232-78794233	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs11637193	chr15:78794235-78794236	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs115782063	chr15:78794250-78794251	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556054775	chr15:78794264-78794265	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs553699236	chr15:78794265-78794266	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575747690	chr15:78794297-78794298	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs568697670	chr15:78794307-78794308	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145964052	chr15:78794322-78794323	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs184251309	chr15:78794342-78794343	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs544444735	chr15:78794369-78794370	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs567940981	chr15:78794400-78794401	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs564350327	chr15:78794442-78794443	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs113520799	chr15:78794482-78794483	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs530875245	chr15:78794510-78794511	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs139932949	chr15:78794538-78794539	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs540351980	chr15:78794640-78794641	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545878390	chr15:78794654-78794655	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117725569	chr15:78794667-78794668	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188668874	chr15:78794680-78794681	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181157728	chr15:78794740-78794741	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35489836	chr15:78794953-78794954	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs561635871	chr15:78795012-78795013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs76361109	chr15:78795014-78795015	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs543974893	chr15:78795031-78795032	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs12914367	chr15:78795032-78795033	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs533005563	chr15:78795056-78795057	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs145545306	chr15:78795063-78795064	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs566506930	chr15:78795094-78795095	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs190593996	chr15:78795095-78795096	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs547351780	chr15:78795097-78795098	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs568734128	chr15:78795115-78795116	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs369758065	chr15:78795117-78795118	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs536074391	chr15:78795226-78795227	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2055587	chr15:78795239-78795240	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs568948715	chr15:78795298-78795299	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569344020	chr15:78795341-78795342	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539971338	chr15:78795348-78795349	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs557951752	chr15:78795375-78795376	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570559675	chr15:78795444-78795445	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs187048903	chr15:78795453-78795454	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548982109	chr15:78795542-78795543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562844662	chr15:78795590-78795591	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533899721	chr15:78795599-78795600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs555263909	chr15:78795609-78795610	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528474817	chr15:78795626-78795627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376213658	chr15:78795630-78795631	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs71148529	chr15:78795648-78795649	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	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
Breast cancer	21364760	CNVD

Chromatin state (count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78732200-78799400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:78755000-78794400	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr15:78755200-78794600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr15:78766000-78799200	Weak transcription	Fetal Heart	heart
5	chr15:78767800-78794200	Strong transcription	Sigmoid Colon	Sigmoid Colon
6	chr15:78772400-78794600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr15:78775600-78794400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:78777000-78799400	Weak transcription	Gastric	stomach
9	chr15:78779200-78799000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr15:78779400-78799200	Weak transcription	Pancreas	Pancrea
11	chr15:78780000-78794200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:78782000-78794400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr15:78782200-78799200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr15:78784800-78794800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:78785600-78799200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr15:78785600-78799200	Weak transcription	Right Ventricle	heart
17	chr15:78785600-78799400	Weak transcription	Spleen	Spleen
18	chr15:78785800-78794600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr15:78785800-78799200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:78787000-78794600	Strong transcription	Fetal Lung	lung
21	chr15:78787400-78795000	Strong transcription	A549	lung
22	chr15:78787400-78799200	Weak transcription	Esophagus	oesophagus
23	chr15:78787400-78799400	Weak transcription	Aorta	Aorta
24	chr15:78787800-78799200	Weak transcription	Right Atrium	heart
25	chr15:78788000-78794600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr15:78788000-78794600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr15:78788000-78794800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr15:78788000-78799200	Weak transcription	Brain Cingulate Gyrus	brain
29	chr15:78788200-78798800	Weak transcription	Fetal Brain Male	brain
30	chr15:78788400-78799200	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr15:78788600-78799200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr15:78788800-78799200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr15:78789000-78799400	Weak transcription	Small Intestine	intestine
34	chr15:78789200-78794400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr15:78789400-78794400	Strong transcription	HSMM	muscle
36	chr15:78789400-78797800	Weak transcription	HSMMtube	muscle
37	chr15:78789600-78799200	Weak transcription	Lung	lung
38	chr15:78790000-78799200	Weak transcription	Stomach Mucosa	stomach
39	chr15:78790600-78799200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr15:78790800-78799200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr15:78790800-78799200	Weak transcription	Rectal Smooth Muscle	rectum
42	chr15:78791000-78799000	Weak transcription	Brain Hippocampus Middle	brain
43	chr15:78791200-78794600	Weak transcription	Brain Germinal Matrix	brain
44	chr15:78791200-78796800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr15:78791200-78799000	Weak transcription	NHLF	lung
46	chr15:78791200-78799200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr15:78791200-78799200	Weak transcription	Brain Substantia Nigra	brain
48	chr15:78791200-78799200	Weak transcription	Colonic Mucosa	Colon
49	chr15:78791200-78799200	Weak transcription	Left Ventricle	heart
50	chr15:78791200-78799400	Weak transcription	GM12878-XiMat	blood

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