Variant report

Variant	nsv832962
Chromosome Location	chr15:33111517-33239736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2021)
CpG islands
(count:1099)
Chromatin interactive
region (count:35)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2021 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:33144871-33145504	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:33159576-33159767	K562	blood:	n/a	n/a
3	ARID3A	chr15:33117119-33117319	HepG2	liver:	n/a	n/a
4	ATF1	chr15:33218767-33218893	K562	blood:	n/a	n/a
5	ATF1	chr15:33172177-33172299	K562	blood:	n/a	n/a
6	ATF1	chr15:33162681-33163010	K562	blood:	n/a	n/a
7	ATF2	chr15:33191348-33191883	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:33200491-33201087	GM12878	blood:	n/a	n/a
9	ATF2	chr15:33191373-33191925	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr15:33142133-33142730	A549	lung:	n/a	n/a
11	ATF3	chr15:33162589-33163012	K562	blood:	n/a	n/a
12	ATF3	chr15:33120617-33121450	A549	lung:	n/a	n/a
13	ATF3	chr15:33116855-33117458	A549	lung:	n/a	n/a
14	ATF3	chr15:33120624-33121446	A549	lung:	n/a	n/a
15	ATF3	chr15:33144841-33145514	A549	lung:	n/a	n/a
16	ATF3	chr15:33142131-33142967	A549	lung:	n/a	n/a
17	BACH1	chr15:33159494-33159789	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:33175656-33175900	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:33175154-33175210	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:33165863-33166308	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:33165875-33166293	K562	blood:	n/a	n/a
22	BACH1	chr15:33164881-33164895	K562	blood:	n/a	n/a
23	BACH1	chr15:33221160-33221387	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr15:33173812-33174063	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr15:33200675-33201039	GM12878	blood:	n/a	n/a
26	BATF	chr15:33216580-33216867	GM12878	blood:	n/a	n/a
27	BATF	chr15:33216573-33216893	GM12878	blood:	n/a	n/a
28	BATF	chr15:33162674-33163028	GM12878	blood:	n/a	chr15:33162820-33162831
29	BATF	chr15:33162661-33162960	GM12878	blood:	n/a	chr15:33162820-33162831
30	BCL11A	chr15:33191354-33191789	H1-hESC	embryonic stem cell:	n/a	chr15:33191642-33191655
31	BCL11A	chr15:33191394-33191852	H1-hESC	embryonic stem cell:	n/a	chr15:33191642-33191655
32	BCL11A	chr15:33200755-33201026	GM12878	blood:	n/a	chr15:33200826-33200835
33	BCL11A	chr15:33162643-33162955	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:33162608-33162974	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:33216557-33216912	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:33200637-33201056	GM12878	blood:	n/a	chr15:33200826-33200835
37	BCL3	chr15:33144880-33145612	A549	lung:	n/a	n/a
38	BCL3	chr15:33116818-33117483	A549	lung:	n/a	n/a
39	BCL3	chr15:33120592-33121549	A549	lung:	n/a	chr15:33120636-33120645
40	BCL3	chr15:33158650-33159539	A549	lung:	n/a	n/a
41	BCL3	chr15:33142110-33142930	A549	lung:	n/a	n/a
42	BCL3	chr15:33116818-33117575	A549	lung:	n/a	n/a
43	BCL3	chr15:33158768-33159753	A549	lung:	n/a	n/a
44	BCL3	chr15:33142119-33142958	A549	lung:	n/a	n/a
45	BCL3	chr15:33120636-33121487	A549	lung:	n/a	chr15:33120636-33120645
46	BCLAF1	chr15:33200479-33201139	GM12878	blood:	n/a	chr15:33200826-33200835
47	BCLAF1	chr15:33216507-33216804	GM12878	blood:	n/a	n/a
48	BHLHE40	chr15:33200447-33201288	GM12878	blood:	n/a	n/a
49	BHLHE40	chr15:33131036-33131292	K562	blood:	n/a	n/a
50	BHLHE40	chr15:33159651-33159697	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:33200866-33200916	HL-60	blood:	n/a
2	chr15:33200866-33200916	HL-60	blood:	n/a
3	chr15:33162876-33162926	HCF	heart:	n/a
4	chr15:33235802-33235852	HCPEpiC	choroid plexus:	n/a
5	chr15:33188759-33188809	NH-A	brain:	n/a
6	chr15:33162876-33162926	HCT-116	colon:	n/a
7	chr15:33235802-33235852	RPTEC	kidney:	n/a
8	chr15:33131642-33131692	HRE	kidney:	n/a
9	chr15:33162876-33162926	HepG2	liver:	n/a
10	chr15:33195247-33195297	AG04449	skin:	fetal
11	chr15:33143407-33143457	PANC-1	pancreas:	n/a
12	chr15:33191698-33191748	T-47D	breast:	n/a
13	chr15:33200866-33200916	HAEpiC	amniotic membrane:	n/a
14	chr15:33188759-33188809	PANC-1	pancreas:	n/a
15	chr15:33165563-33165613	PFSK-1	brain:	n/a
16	chr15:33131642-33131692	GM12891	blood:	n/a
17	chr15:33178652-33178702	MCF10A-Er-Src	breast:	n/a
18	chr15:33235802-33235852	PANC-1	pancreas:	n/a
19	chr15:33200866-33200916	ovcar-3	ovarian:	n/a
20	chr15:33125028-33125078	AoSMC	blood vessel:	n/a
21	chr15:33179514-33179564	AoSMC	blood vessel:	n/a
22	chr15:33165563-33165613	NH-A	brain:	n/a
23	chr15:33131642-33131692	HRCEpiC	kidney:	n/a
24	chr15:33165563-33165613	PrEC	prostate:	n/a
25	chr15:33220732-33220782	RPTEC	kidney:	n/a
26	chr15:33125028-33125078	AG09309	skin:	n/a
27	chr15:33162876-33162926	HIPEpiC	eye:	n/a
28	chr15:33171339-33171389	AG04450	lung:	fetal
29	chr15:33177867-33177917	LNCaP	prostate:	n/a
30	chr15:33200866-33200916	HCF	heart:	n/a
31	chr15:33195247-33195297	GM12878	blood:	n/a
32	chr15:33188759-33188809	IMR90	lung:	fetal
33	chr15:33195247-33195297	AG10803	skin:	n/a
34	chr15:33178652-33178702	RPTEC	kidney:	n/a
35	chr15:33220732-33220782	ECC-1	luminal epithelium:	n/a
36	chr15:33177867-33177917	HRCEpiC	kidney:	n/a
37	chr15:33195247-33195297	HCM	heart:	n/a
38	chr15:33162876-33162926	HEK293	kidney:	embryo
39	chr15:33178652-33178702	BE2_C	brain:	n/a
40	chr15:33154262-33154312	NHBE	bronchial:	n/a
41	chr15:33148913-33148963	IMR90	lung:	fetal
42	chr15:33195247-33195297	GM12892	blood:	n/a
43	chr15:33235802-33235852	PrEC	prostate:	n/a
44	chr15:33165563-33165613	U87	brain:	n/a
45	chr15:33125028-33125078	BE2_C	brain:	n/a
46	chr15:33154262-33154312	HCPEpiC	choroid plexus:	n/a
47	chr15:33211107-33211157	SK-N-MC	brain:	n/a
48	chr15:33162876-33162926	LNCaP	prostate:	n/a
49	chr15:33154262-33154312	GM12891	blood:	n/a
50	chr15:33188759-33188809	PrEC	prostate:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:33237429..33239397-chr15:33241975..33243636,2	MCF-7	breast:
2	chr15:33136574..33137426-chr15:33228228..33228738,2	K562	blood:
3	chr15:33141128..33142797-chr15:33145932..33148761,2	K562	blood:
4	chr15:33136039..33136889-chr15:33228248..33228998,3	MCF-7	breast:
5	chr15:33203701..33205590-chr15:33205602..33207495,2	MCF-7	breast:
6	chr15:33148021..33149698-chr15:33359927..33361500,2	MCF-7	breast:
7	chr15:33232993..33235695-chr15:33238081..33239940,2	K562	blood:
8	chr15:33203701..33205590-chr15:33205602..33207495,2	MCF-7	breast:
9	chr15:33232993..33235695-chr15:33238081..33239940,2	K562	blood:
10	chr15:33159839..33162457-chr15:33167259..33169460,2	K562	blood:
11	chr15:33111785..33114105-chr15:33134762..33137156,2	K562	blood:
12	chr15:33191578..33193662-chr15:33205151..33207936,2	MCF-7	breast:
13	chr15:33136051..33136687-chr15:33424687..33425559,2	K562	blood:
14	chr15:33159839..33162457-chr15:33167259..33169460,2	K562	blood:
15	chr15:33111785..33114105-chr15:33134762..33137156,2	K562	blood:
16	chr15:33131473..33134242-chr15:33135502..33137920,3	K562	blood:
17	chr15:32954517..32955503-chr15:33228158..33229122,2	MCF-7	breast:
18	chr15:33142290..33144094-chr15:33145856..33147820,2	MCF-7	breast:
19	chr15:33141128..33142797-chr15:33145932..33148761,2	K562	blood:
20	chr15:33131473..33134242-chr15:33135502..33137920,3	K562	blood:
21	chr15:33191578..33193662-chr15:33205151..33207936,2	MCF-7	breast:
22	chr15:33177002..33179276-chr15:33196689..33199398,2	K562	blood:
23	chr15:33142290..33144094-chr15:33145856..33147820,2	MCF-7	breast:
24	chr15:32954209..32955138-chr15:33136364..33136960,2	MCF-7	breast:
25	chr15:33177002..33179276-chr15:33196689..33199398,2	K562	blood:
26	chr15:33136039..33136889-chr15:33228248..33228998,3	MCF-7	breast:
27	chr15:33136574..33137426-chr15:33228228..33228738,2	K562	blood:
28	chr15:33136011..33136698-chr15:33286980..33287655,2	K562	blood:
29	chr15:33194367..33197072-chr15:33201375..33203984,2	MCF-7	breast:
30	chr15:33152788..33155505-chr15:33160660..33163285,2	K562	blood:
31	chr15:33126321..33128802-chr15:33129719..33131758,2	K562	blood:
32	chr15:33126321..33128802-chr15:33129719..33131758,2	K562	blood:
33	chr15:33148879..33150784-chr15:33151258..33154124,2	K562	blood:
34	chr15:33191297..33193263-chr15:33193347..33195988,2	K562	blood:
35	chr15:33194367..33197072-chr15:33201375..33203984,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-632K20.1.1-3	chr15:33129184-33129527	NONHSAT041533

No data

Variant related genes	Relation type
FMN1	TF binding region
ENSG00000238342	TF binding region
ENSG00000259392	TF binding region
FMN1	CpG island
ENSG00000238342	CpG island
ENSG00000259392	CpG island
ENSG00000248905	chromatin interactions

Extended variants
information (count: 6088 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6088 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75283997	chr15:33111525-33111526	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs571967200	chr15:33111569-33111570	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs539379470	chr15:33111587-33111588	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs149820568	chr15:33111589-33111590	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs116371670	chr15:33111595-33111596	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs148954157	chr15:33111597-33111598	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs555401577	chr15:33111638-33111639	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573660653	chr15:33111641-33111642	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541220630	chr15:33111681-33111682	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552791535	chr15:33111695-33111696	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147072841	chr15:33111830-33111831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147695287	chr15:33111850-33111851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7174816	chr15:33111929-33111930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372307025	chr15:33111941-33111942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190485845	chr15:33111954-33111955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542662976	chr15:33111957-33111958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35303714	chr15:33111962-33111963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs62001287	chr15:33112053-33112054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74011839	chr15:33112106-33112107	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs181758380	chr15:33112157-33112158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563238486	chr15:33112191-33112192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547205701	chr15:33112218-33112219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565494083	chr15:33112277-33112278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs72486668	chr15:33112299-33112300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs545552910	chr15:33112314-33112315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553298142	chr15:33112343-33112344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186931694	chr15:33112365-33112366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560328196	chr15:33112386-33112387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148050938	chr15:33112432-33112433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs57264322	chr15:33112438-33112439	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs73386848	chr15:33112465-33112466	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs114044963	chr15:33112530-33112531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188657184	chr15:33112550-33112551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534455106	chr15:33112554-33112555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561343238	chr15:33112634-33112635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141807037	chr15:33112660-33112661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577387338	chr15:33112678-33112679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs528924127	chr15:33112685-33112686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181293578	chr15:33112696-33112697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs61355906	chr15:33112717-33112718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111363062	chr15:33112720-33112721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575450230	chr15:33112729-33112730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201292390	chr15:33112731-33112732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371062617	chr15:33112744-33112745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561165534	chr15:33112776-33112777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs16959173	chr15:33112815-33112816	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189919000	chr15:33112832-33112833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150135311	chr15:33112834-33112835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs17228808	chr15:33112854-33112855	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs551199786	chr15:33112892-33112893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1935 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33061200-33141000	Weak transcription	Placenta	Placenta
2	chr15:33096200-33154000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr15:33096400-33116200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:33096400-33159000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr15:33103800-33139200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:33110800-33111800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr15:33110800-33112000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr15:33110800-33114000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:33111000-33111600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr15:33111000-33111600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:33111000-33111600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr15:33111000-33111600	Flanking Active TSS	A549	lung
13	chr15:33111000-33111800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr15:33111000-33111800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr15:33111000-33111800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr15:33111000-33111800	Flanking Active TSS	NHDF-Ad	bronchial
17	chr15:33111000-33111800	Enhancers	NHEK	skin
18	chr15:33111200-33111600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr15:33111200-33111600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr15:33111200-33111600	Enhancers	Gastric	stomach
21	chr15:33111200-33111600	Enhancers	Pancreas	Pancrea
22	chr15:33111200-33111600	Flanking Active TSS	NHLF	lung
23	chr15:33111200-33111800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr15:33111200-33111800	Flanking Active TSS	NH-A	brain
25	chr15:33111200-33111800	Flanking Active TSS	Osteobl	bone
26	chr15:33111200-33112400	Enhancers	Fetal Stomach	stomach
27	chr15:33111200-33112400	Enhancers	HSMM	muscle
28	chr15:33111200-33130000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr15:33111400-33111600	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr15:33111400-33111800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr15:33111400-33111800	Enhancers	HSMMtube	muscle
32	chr15:33111400-33112200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr15:33111400-33112200	Enhancers	Fetal Kidney	kidney
34	chr15:33111400-33114200	Enhancers	HUVEC	blood vessel
35	chr15:33111400-33116000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr15:33111600-33111800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr15:33111600-33112000	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr15:33111600-33112000	Enhancers	NHLF	lung
39	chr15:33111600-33112200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr15:33111600-33112400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr15:33111600-33113400	Enhancers	A549	lung
42	chr15:33111600-33115200	Weak transcription	Pancreas	Pancrea
43	chr15:33111600-33116200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr15:33111600-33118400	Weak transcription	Gastric	stomach
45	chr15:33111800-33112000	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr15:33111800-33112200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr15:33111800-33112600	Enhancers	NH-A	brain
48	chr15:33111800-33113200	Enhancers	NHDF-Ad	bronchial
49	chr15:33111800-33113200	Enhancers	Osteobl	bone
50	chr15:33111800-33113600	Enhancers	Muscle Satellite Cultured Cells	--

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