Variant report

Variant	esv3326516
Chromosome Location	chr15:79090897-79093445
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	BATF	chr15:79091206-79091465	GM12878	blood:	n/a	n/a
2	CEBPB	chr15:79090821-79091015	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr15:79093293-79093431	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr15:79091371-79091499	GM20000	blood:	n/a	n/a
5	CTCF	chr15:79093340-79093490	GM12868	blood:	n/a	n/a
6	CTCF	chr15:79090900-79091050	BJ	skin:	n/a	n/a
7	CTCF	chr15:79093280-79093430	GM12865	blood:	n/a	n/a
8	CTCF	chr15:79093400-79093550	HepG2	liver:	n/a	n/a
9	E2F6	chr15:79092505-79092668	K562	blood:	n/a	n/a
10	FOS	chr15:79090919-79090996	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr15:79090828-79091088	MCF10A-Er-Src	breast:	n/a	n/a
12	FOSL2	chr15:79090705-79091125	A549	lung:	n/a	n/a
13	JUND	chr15:79090717-79091065	A549	lung:	n/a	n/a
14	JUND	chr15:79090671-79091153	A549	lung:	n/a	n/a
15	JUND	chr15:79090772-79091045	Hela-S3	cervix:	n/a	n/a
16	MAX	chr15:79090823-79090972	Hela-S3	cervix:	n/a	n/a
17	MAZ	chr15:79090831-79091068	Hela-S3	cervix:	n/a	n/a
18	MYC	chr15:79090902-79090998	MCF10A-Er-Src	breast:	n/a	n/a
19	NR3C1	chr15:79090807-79091137	ECC-1	luminal epithelium:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
20	NR3C1	chr15:79090708-79091240	A549	lung:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
21	NR3C1	chr15:79090412-79091255	A549	lung:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
22	NR3C1	chr15:79090761-79091160	A549	lung:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
23	NR3C1	chr15:79090886-79091133	ECC-1	luminal epithelium:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
24	NR3C1	chr15:79090163-79091279	A549	lung:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090263-79090276 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
25	NR3C1	chr15:79090205-79091265	A549	lung:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090263-79090276 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
26	NR3C1	chr15:79090840-79091097	A549	lung:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
27	NR3C1	chr15:79090679-79091263	A549	lung:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
28	NR3C1	chr15:79090250-79091263	A549	lung:	n/a	chr15:79090984-79091000 chr15:79090985-79090999 chr15:79090989-79091002 chr15:79090979-79091005 chr15:79090979-79091005 chr15:79090984-79091000 chr15:79090263-79090276 chr15:79090984-79091000 chr15:79090984-79091000 chr15:79090979-79091005 chr15:79090985-79090999
29	POLR2A	chr15:79090749-79091144	Gliobla	brain:	n/a	n/a
30	POLR2A	chr15:79090738-79091108	U87	brain:	n/a	n/a
31	POLR2A	chr15:79090626-79091166	U87	brain:	n/a	n/a
32	POLR2A	chr15:79090672-79091144	A549	lung:	n/a	n/a
33	RCOR1	chr15:79090772-79091039	Hela-S3	cervix:	n/a	n/a
34	RFX5	chr15:79090796-79090971	Hela-S3	cervix:	n/a	n/a
35	SP1	chr15:79090637-79091126	A549	lung:	n/a	chr15:79091076-79091088 chr15:79091078-79091087 chr15:79091073-79091087 chr15:79091077-79091086 chr15:79091076-79091088
36	TCF3	chr15:79092375-79092743	GM12878	blood:	n/a	n/a
37	TFAP2A	chr15:79090368-79091121	Hela-S3	cervix:	n/a	chr15:79090912-79090927
38	TFAP2C	chr15:79090288-79091182	Hela-S3	cervix:	n/a	chr15:79090816-79090831
39	USF1	chr15:79090698-79091108	A549	lung:	n/a	n/a
40	YY1	chr15:79090627-79091131	A549	lung:	n/a	n/a
41	ZNF217	chr15:79090834-79090996	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:79092558-79092608	NT2-D1	testis:	n/a
2	chr15:79090958-79091008	HL-60	blood:	n/a
3	chr15:79092558-79092608	HCF	heart:	n/a
4	chr15:79092558-79092608	GM12891	blood:	n/a
5	chr15:79092743-79092793	Hela-S3	cervix:	n/a
6	chr15:79092743-79092793	ECC-1	luminal epithelium:	n/a
7	chr15:79092878-79092928	T-47D	breast:	n/a
8	chr15:79092743-79092793	GM06990	blood:	n/a
9	chr15:79092878-79092928	HEEpiC	esophagus:	n/a
10	chr15:79090958-79091008	HRE	kidney:	n/a
11	chr15:79092743-79092793	PFSK-1	brain:	n/a
12	chr15:79090958-79091008	ovcar-3	ovarian:	n/a
13	chr15:79092743-79092793	AG04450	lung:	fetal
14	chr15:79092878-79092928	ECC-1	luminal epithelium:	n/a
15	chr15:79092743-79092793	SAEC	small airway:	n/a
16	chr15:79092558-79092608	AG04450	lung:	fetal
17	chr15:79090958-79091008	NHBE	bronchial:	n/a
18	chr15:79092558-79092608	HCM	heart:	n/a
19	chr15:79092558-79092608	HCT-116	colon:	n/a
20	chr15:79090958-79091008	ProgFib	skin:	n/a
21	chr15:79090958-79091008	HCT-116	colon:	n/a
22	chr15:79092558-79092608	HEK293	kidney:	embryo
23	chr15:79092878-79092928	NHDF-neo	bronchial:	n/a
24	chr15:79092558-79092608	K562	blood:	n/a
25	chr15:79092878-79092928	H1-hESC	embryonic stem cell:	embryo
26	chr15:79090958-79091008	U87	brain:	n/a
27	chr15:79092743-79092793	AG09309	skin:	n/a
28	chr15:79092558-79092608	Jurkat	blood:	n/a
29	chr15:79092743-79092793	Caco-2	colon:	n/a
30	chr15:79092878-79092928	GM12891	blood:	n/a
31	chr15:79090958-79091008	MCF-7	breast:	n/a
32	chr15:79092558-79092608	NB4	blood:	n/a
33	chr15:79090958-79091008	HEEpiC	esophagus:	n/a
34	chr15:79092878-79092928	NB4	blood:	n/a
35	chr15:79090958-79091008	PrEC	prostate:	n/a
36	chr15:79092743-79092793	PANC-1	pancreas:	n/a
37	chr15:79092878-79092928	HIPEpiC	eye:	n/a
38	chr15:79092878-79092928	AG04449	skin:	fetal
39	chr15:79092558-79092608	PFSK-1	brain:	n/a
40	chr15:79092558-79092608	Hepatocyte	liver:	n/a
41	chr15:79090958-79091008	SKMC	muscle:	n/a
42	chr15:79092743-79092793	K562	blood:	n/a
43	chr15:79092743-79092793	SK-N-MC	brain:	n/a
44	chr15:79092878-79092928	AG09319	gingival:	n/a
45	chr15:79092558-79092608	HUVEC	blood vessel:	n/a
46	chr15:79090958-79091008	SK-N-MC	brain:	n/a
47	chr15:79090958-79091008	PANC-1	pancreas:	n/a
48	chr15:79092743-79092793	HCF	heart:	n/a
49	chr15:79092878-79092928	HUVEC	blood vessel:	n/a
50	chr15:79092743-79092793	AG09319	gingival:	n/a

Variant related genes	Relation type
ADAMTS7	TF binding region
ADAMTS7	CpG island

Extended variants
information (count: 97 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554196018	chr15:79090910-79090911	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs572684288	chr15:79090911-79090912	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs542854413	chr15:79090918-79090919	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs200543264	chr15:79090947-79090948	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs551035757	chr15:79090950-79090951	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554741863	chr15:79090962-79090963	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs576180734	chr15:79090978-79090979	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs541313866	chr15:79090980-79090981	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs565346171	chr15:79090995-79090996	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs35330689	chr15:79091026-79091027	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs191466446	chr15:79091060-79091061	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs115793377	chr15:79091083-79091084	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs559419427	chr15:79091159-79091160	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs530004649	chr15:79091165-79091166	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs146298934	chr15:79091166-79091167	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs561088769	chr15:79091188-79091189	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs569876966	chr15:79091218-79091219	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530691796	chr15:79091286-79091287	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552325632	chr15:79091344-79091345	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371066570	chr15:79091422-79091423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529881979	chr15:79091437-79091438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534355346	chr15:79091452-79091453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552924658	chr15:79091454-79091455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566292293	chr15:79091543-79091544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543514272	chr15:79091600-79091601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563190408	chr15:79091605-79091606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532229670	chr15:79091674-79091675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79380888	chr15:79091790-79091791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79734971	chr15:79091795-79091796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs71407295	chr15:79091809-79091810	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs71407296	chr15:79091821-79091822	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs71407297	chr15:79091826-79091827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71407298	chr15:79091833-79091834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150632519	chr15:79091845-79091846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576244021	chr15:79091874-79091875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71407299	chr15:79091875-79091876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543581337	chr15:79091884-79091885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71448830	chr15:79091897-79091898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185580238	chr15:79091950-79091951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541105449	chr15:79091990-79091991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567533105	chr15:79092007-79092008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190042562	chr15:79092075-79092076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563089296	chr15:79092179-79092180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs202148592	chr15:79092182-79092183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11638321	chr15:79092183-79092184	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563548721	chr15:79092185-79092186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181460943	chr15:79092193-79092194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114897452	chr15:79092243-79092244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564066994	chr15:79092281-79092282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528187819	chr15:79092334-79092335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79072000-79096600	Weak transcription	Brain Substantia Nigra	brain
2	chr15:79072000-79096800	Weak transcription	Colon Smooth Muscle	Colon
3	chr15:79072800-79102400	Weak transcription	Fetal Kidney	kidney
4	chr15:79077200-79096600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:79078200-79093200	Strong transcription	Fetal Stomach	stomach
6	chr15:79078400-79091800	Weak transcription	Gastric	stomach
7	chr15:79079400-79091000	Weak transcription	HUVEC	blood vessel
8	chr15:79080400-79096200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr15:79080800-79095200	Weak transcription	Fetal Intestine Large	intestine
10	chr15:79082800-79096200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr15:79082800-79102200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr15:79083200-79102000	Weak transcription	Fetal Heart	heart
13	chr15:79083800-79102400	Weak transcription	Aorta	Aorta
14	chr15:79086000-79091000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr15:79086200-79091400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr15:79088200-79094000	Weak transcription	Lung	lung
17	chr15:79088200-79096800	Weak transcription	Brain Angular Gyrus	brain
18	chr15:79088600-79093400	Weak transcription	Spleen	Spleen
19	chr15:79088600-79096400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr15:79088800-79102600	Weak transcription	Ovary	ovary
21	chr15:79089200-79091200	Enhancers	Hela-S3	cervix
22	chr15:79089400-79096000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr15:79089600-79091200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr15:79089600-79091400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:79089800-79091000	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr15:79089800-79091200	Enhancers	HMEC	breast
27	chr15:79090000-79091000	Enhancers	Placenta	Placenta
28	chr15:79090000-79091200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr15:79090000-79091200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:79090000-79091200	Enhancers	Right Atrium	heart
31	chr15:79090000-79096400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr15:79090200-79091200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr15:79090200-79091200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:79090200-79091200	Enhancers	NHDF-Ad	bronchial
35	chr15:79090200-79096400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr15:79090200-79101000	Weak transcription	Fetal Lung	lung
37	chr15:79090200-79101000	Weak transcription	Stomach Smooth Muscle	stomach
38	chr15:79090400-79091000	Enhancers	Adipose Nuclei	Adipose
39	chr15:79090400-79091000	Enhancers	NHEK	skin
40	chr15:79090400-79091200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr15:79090400-79091200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr15:79090400-79091200	Enhancers	Fetal Muscle Leg	muscle
43	chr15:79090400-79091200	Enhancers	NHLF	lung
44	chr15:79090400-79091200	Enhancers	Osteobl	bone
45	chr15:79090400-79095600	Weak transcription	Fetal Intestine Small	intestine
46	chr15:79090400-79096200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr15:79090400-79096200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr15:79090400-79096200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr15:79090400-79096400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr15:79090400-79096400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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