Variant report

Variant	nsv1039906
Chromosome Location	chr15:41476209-41518976
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	ARID3A	chr15:41477142-41477342	K562	blood:	n/a	n/a
2	ARID3A	chr15:41477064-41477380	HepG2	liver:	n/a	n/a
3	BHLHE40	chr15:41497729-41497756	K562	blood:	n/a	n/a
4	CEBPB	chr15:41490045-41490276	IMR90	lung:	n/a	chr15:41490172-41490183
5	CEBPB	chr15:41490084-41490252	H1-hESC	embryonic stem cell:	n/a	chr15:41490172-41490183
6	CEBPB	chr15:41490136-41490265	A549	lung:	n/a	chr15:41490172-41490183
7	CEBPB	chr15:41482587-41482794	Hela-S3	cervix:	n/a	chr15:41482717-41482730 chr15:41482629-41482640 chr15:41482719-41482730
8	CEBPB	chr15:41482549-41482798	H1-hESC	embryonic stem cell:	n/a	chr15:41482717-41482730 chr15:41482629-41482640 chr15:41482719-41482730
9	CEBPB	chr15:41478566-41478673	IMR90	lung:	n/a	n/a
10	CEBPB	chr15:41501176-41501378	K562	blood:	n/a	chr15:41501280-41501293 chr15:41501281-41501292
11	CEBPB	chr15:41482572-41482731	K562	blood:	n/a	chr15:41482717-41482730 chr15:41482629-41482640 chr15:41482719-41482730
12	CEBPB	chr15:41482514-41482852	IMR90	lung:	n/a	chr15:41482717-41482730 chr15:41482629-41482640 chr15:41482719-41482730
13	CEBPB	chr15:41482513-41482793	K562	blood:	n/a	chr15:41482717-41482730 chr15:41482629-41482640 chr15:41482719-41482730
14	CEBPB	chr15:41490074-41490200	HepG2	liver:	n/a	chr15:41490172-41490183
15	CEBPB	chr15:41482605-41482656	A549	lung:	n/a	chr15:41482629-41482640
16	CEBPB	chr15:41482525-41482802	HepG2	liver:	n/a	chr15:41482717-41482730 chr15:41482629-41482640 chr15:41482719-41482730
17	CEBPB	chr15:41501166-41501417	Hela-S3	cervix:	n/a	chr15:41501280-41501293 chr15:41501281-41501292
18	CEBPB	chr15:41490085-41490289	K562	blood:	n/a	chr15:41490172-41490183
19	CEBPB	chr15:41482524-41482806	K562	blood:	n/a	chr15:41482717-41482730 chr15:41482629-41482640 chr15:41482719-41482730
20	CEBPB	chr15:41490095-41490283	HepG2	liver:	n/a	chr15:41490172-41490183
21	CEBPB	chr15:41501199-41501340	IMR90	lung:	n/a	chr15:41501280-41501293 chr15:41501281-41501292
22	CEBPB	chr15:41501207-41501344	HepG2	liver:	n/a	chr15:41501280-41501293 chr15:41501281-41501292
23	CTCF	chr15:41477128-41477375	Kidney_OC	kidney:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
24	CTCF	chr15:41487480-41487730	GM06990	blood:	n/a	n/a
25	CTCF	chr15:41477100-41477250	GM12864	blood:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
26	CTCF	chr15:41477160-41477310	BJ	skin:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
27	CTCF	chr15:41487460-41487610	GM12875	blood:	n/a	n/a
28	CTCF	chr15:41477160-41477310	Hela-S3	cervix:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
29	CTCF	chr15:41477158-41477213	MCF-7	breast:	n/a	n/a
30	CTCF	chr15:41477140-41477290	BE2_C	brain:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
31	CTCF	chr15:41477140-41477290	GM12871	blood:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
32	CTCF	chr15:41477180-41477330	AG09319	gingival:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
33	CTCF	chr15:41487340-41487490	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr15:41476400-41476550	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr15:41477138-41477300	LNCaP	prostate:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
36	CTCF	chr15:41491375-41491409	GM20000	blood:	n/a	n/a
37	CTCF	chr15:41487400-41487550	GM12865	blood:	n/a	n/a
38	CTCF	chr15:41487400-41487550	GM12874	blood:	n/a	n/a
39	CTCF	chr15:41487280-41487430	GM12868	blood:	n/a	n/a
40	CTCF	chr15:41487420-41487570	MCF-7	breast:	n/a	n/a
41	CTCF	chr15:41477162-41477265	GM13976	blood:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
42	CTCF	chr15:41477141-41477303	GM10248	blood:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
43	CTCF	chr15:41477160-41477310	GM12875	blood:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
44	CTCF	chr15:41477180-41477330	HPAF	blood vessel:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
45	CTCF	chr15:41477180-41477330	AG10803	skin:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
46	CTCF	chr15:41487400-41487550	HCFaa	heart:	n/a	n/a
47	CTCF	chr15:41477140-41477290	HEEpiC	esophagus:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
48	CTCF	chr15:41487360-41487510	GM12866	blood:	n/a	n/a
49	CTCF	chr15:41477117-41477337	Hela-S3	cervix:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234
50	CTCF	chr15:41477102-41477362	HUVEC	blood vessel:	n/a	chr15:41477218-41477236 chr15:41477219-41477235 chr15:41477213-41477234

No.	Distal block	Cell Line	Cell type
1	chr15:41195697..41196981-chr15:41476244..41477668,8	K562	blood:
2	chr15:41507375..41509488-chr15:41521656..41523869,2	MCF-7	breast:
3	chr15:41511538..41514696-chr15:41517185..41519800,3	K562	blood:
4	chr15:41476395..41478011-chr15:41481454..41483505,2	K562	blood:
5	chr15:41493527..41495439-chr15:41497642..41500215,2	K562	blood:
6	chr15:41198416..41199217-chr15:41476755..41477711,4	K562	blood:
7	chr15:41045965..41048868-chr15:41482776..41485356,2	K562	blood:
8	chr15:41511864..41514825-chr15:41521653..41523224,2	K562	blood:
9	chr15:41517146..41518723-chr15:41521956..41524781,2	K562	blood:
10	chr15:41206351..41206914-chr15:41476761..41477648,2	K562	blood:
11	chr15:41511538..41514696-chr15:41517185..41519800,3	K562	blood:
12	chr15:41493527..41495439-chr15:41497642..41500215,2	K562	blood:
13	chr15:41512004..41513942-chr15:41524174..41526665,2	K562	blood:
14	chr15:41366851..41369456-chr15:41474724..41476763,2	K562	blood:
15	chr15:41506769..41509087-chr15:41627220..41629152,2	K562	blood:
16	chr15:41511538..41516439-chr15:41517024..41523224,9	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC012652.1.1-5	chr15:41485541-41487747	predAs_engstrom06_AA043058_1
2	lnc-AC012652.1.1-4	chr15:41487791-41489261	predAs_engstrom06_AA009975_1
3	lnc-INO80-3	chr15:41484165-41484463	NONHSAT041916

Variant related genes	Relation type
RN7SL497P	TF binding region
CHP1	TF binding region
EXD1	TF binding region
ENSG00000178997	chromatin interactions
ENSG00000251161	chromatin interactions
ENSG00000187446	chromatin interactions
ENSG00000137824	chromatin interactions

Extended variants
information (count: 1293 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs522063	chr15:41476209-41476210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200051315	chr15:41476216-41476217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377285853	chr15:41476245-41476246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370572579	chr15:41476247-41476248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551890183	chr15:41476266-41476267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185697361	chr15:41476287-41476288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs199676061	chr15:41476288-41476289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376151891	chr15:41476298-41476299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147079267	chr15:41476328-41476329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369400894	chr15:41476332-41476333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150875623	chr15:41476422-41476423	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190768484	chr15:41476453-41476454	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs690733	chr15:41476465-41476466	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs374548709	chr15:41476470-41476471	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143293058	chr15:41476472-41476473	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs17852789	chr15:41476480-41476481	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs367752504	chr15:41476545-41476546	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146685114	chr15:41476551-41476552	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs139103015	chr15:41476552-41476553	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs143955302	chr15:41476593-41476594	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200816556	chr15:41476625-41476626	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145139071	chr15:41476630-41476631	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149108859	chr15:41476641-41476642	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201880604	chr15:41476668-41476669	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372898407	chr15:41476670-41476671	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369993026	chr15:41476678-41476679	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576612217	chr15:41476709-41476710	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566932891	chr15:41476714-41476715	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544379314	chr15:41476729-41476730	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs186855358	chr15:41476733-41476734	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527801980	chr15:41476734-41476735	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377668115	chr15:41476744-41476745	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143148566	chr15:41476777-41476778	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540188349	chr15:41476788-41476789	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs375799345	chr15:41476806-41476807	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111604343	chr15:41476856-41476857	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs11454626	chr15:41476857-41476858	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs201463455	chr15:41476870-41476871	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs199650565	chr15:41476871-41476872	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs386783389	chr15:41476875-41476876	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs576807188	chr15:41476876-41476877	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs183883605	chr15:41476889-41476890	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562197208	chr15:41476913-41476914	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs531316266	chr15:41476915-41476916	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370938351	chr15:41476916-41476917	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533864531	chr15:41476921-41476922	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527970075	chr15:41476987-41476988	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs547816779	chr15:41476997-41476998	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs570821985	chr15:41477004-41477005	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539401027	chr15:41477007-41477008	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41474400-41476800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr15:41474600-41476600	Enhancers	Osteobl	bone
3	chr15:41475600-41476800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr15:41475600-41476800	Enhancers	A549	lung
5	chr15:41475800-41476400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr15:41475800-41476800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:41475800-41476800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr15:41476000-41476400	Enhancers	H1 Cell Line	embryonic stem cell
9	chr15:41476000-41476400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr15:41476000-41476400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr15:41476000-41476400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr15:41476000-41476600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr15:41476000-41476600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr15:41476000-41476600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr15:41476000-41476800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr15:41476000-41476800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr15:41476000-41476800	Enhancers	NH-A	brain
18	chr15:41476000-41476800	Enhancers	NHLF	lung
19	chr15:41476200-41476400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr15:41476200-41476400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr15:41476200-41476800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr15:41476200-41476800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr15:41476400-41478200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr15:41477200-41477400	Enhancers	Primary B cells from peripheral blood	blood
25	chr15:41478200-41478400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:41480400-41480800	Enhancers	Fetal Brain Male	brain
27	chr15:41482200-41482600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr15:41482200-41483000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr15:41482200-41483000	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr15:41482200-41483200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr15:41482600-41482800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr15:41482600-41483000	Enhancers	Adipose Nuclei	Adipose
33	chr15:41482600-41483000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr15:41482800-41483000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:41483600-41484400	Enhancers	Colon Smooth Muscle	Colon
36	chr15:41484000-41484200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr15:41484200-41484400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr15:41484400-41494400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr15:41490200-41490600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr15:41497400-41497600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:41497400-41497800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr15:41497400-41497800	Enhancers	K562	blood
43	chr15:41497600-41499800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr15:41497800-41499800	Weak transcription	K562	blood
45	chr15:41499400-41499600	Enhancers	HMEC	breast
46	chr15:41499400-41499800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr15:41499600-41499800	Enhancers	NHEK	skin
48	chr15:41499600-41500000	Flanking Active TSS	HMEC	breast
49	chr15:41499800-41500000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr15:41499800-41500000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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