Variant report

Variant	esv1834529
Chromosome Location	chr5:147442199-147456843
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	CEBPB	chr5:147443606-147443759	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr5:147447760-147447910	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr5:147453700-147453850	BE2_C	brain:	n/a	n/a
4	E2F4	chr5:147443606-147443961	MCF10A-Er-Src	breast:	n/a	n/a
5	ESR1	chr5:147449960-147450380	T-47D	breast:	n/a	chr5:147450140-147450157
6	ESR1	chr5:147449920-147450370	T-47D	breast:	n/a	chr5:147450140-147450157
7	ESR1	chr5:147449966-147450390	T-47D	breast:	n/a	chr5:147450140-147450157
8	ESR1	chr5:147449990-147450322	T-47D	breast:	n/a	chr5:147450140-147450157
9	ESR1	chr5:147449970-147450341	T-47D	breast:	n/a	chr5:147450140-147450157
10	ESR1	chr5:147449855-147450362	T-47D	breast:	n/a	chr5:147450140-147450157
11	FOS	chr5:147452054-147452415	MCF10A-Er-Src	breast:	n/a	chr5:147452270-147452281
12	FOS	chr5:147443430-147443906	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr5:147443477-147443961	MCF10A-Er-Src	breast:	n/a	chr5:147443913-147443925
14	FOS	chr5:147451872-147452314	MCF10A-Er-Src	breast:	n/a	chr5:147452270-147452281
15	FOS	chr5:147451884-147452432	MCF10A-Er-Src	breast:	n/a	chr5:147452270-147452281
16	FOS	chr5:147451896-147452429	MCF10A-Er-Src	breast:	n/a	chr5:147452270-147452281
17	FOS	chr5:147443460-147443966	MCF10A-Er-Src	breast:	n/a	chr5:147443913-147443925
18	FOS	chr5:147443456-147443906	MCF10A-Er-Src	breast:	n/a	n/a
19	FOXA1	chr5:147450117-147450335	T-47D	breast:	n/a	n/a
20	FOXA1	chr5:147451657-147451922	T-47D	breast:	n/a	n/a
21	GATA3	chr5:147447786-147447986	SH-SY5Y	brain:	n/a	n/a
22	GATA3	chr5:147450038-147450197	MCF-7	breast:	n/a	n/a
23	GATA3	chr5:147450008-147450383	T-47D	breast:	n/a	n/a
24	MAFF	chr5:147455117-147455455	HepG2	liver:	n/a	chr5:147455280-147455298
25	MAFF	chr5:147455173-147455373	K562	blood:	n/a	chr5:147455280-147455298
26	MAFK	chr5:147455122-147455450	IMR90	lung:	n/a	chr5:147455282-147455297
27	MAFK	chr5:147455121-147455469	HepG2	liver:	n/a	chr5:147455282-147455297
28	MAFK	chr5:147455255-147455333	K562	blood:	n/a	chr5:147455282-147455297
29	MAFK	chr5:147455111-147455476	HepG2	liver:	n/a	chr5:147455282-147455297
30	MAFK	chr5:147455236-147455388	H1-hESC	embryonic stem cell:	n/a	chr5:147455282-147455297
31	MAZ	chr5:147446575-147446681	HepG2	liver:	n/a	n/a
32	MYC	chr5:147443456-147443880	MCF10A-Er-Src	breast:	n/a	n/a
33	MYC	chr5:147443518-147443884	MCF10A-Er-Src	breast:	n/a	n/a
34	MYC	chr5:147451859-147452242	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr5:147442558-147442601	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr5:147446601-147446650	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr5:147451795-147452802	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr5:147443531-147443765	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr5:147451864-147452250	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr5:147443613-147443864	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr5:147443536-147443671	Gliobla	brain:	n/a	n/a
42	POLR2A	chr5:147447354-147447362	MCF10A-Er-Src	breast:	n/a	n/a
43	SETDB1	chr5:147456195-147456571	U2OS	brain:	n/a	n/a
44	STAT3	chr5:147443530-147443885	MCF10A-Er-Src	breast:	n/a	n/a
45	STAT3	chr5:147445807-147445818	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr5:147443566-147444057	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr5:147447773-147447858	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr5:147443538-147443919	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr5:147451853-147452432	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr5:147445608-147445651	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:147443067-147443117	SK-N-SH	brain:	n/a
2	chr5:147443284-147443334	GM06990	blood:	n/a
3	chr5:147443284-147443334	ovcar-3	ovarian:	n/a
4	chr5:147443067-147443117	HCM	heart:	n/a
5	chr5:147443284-147443334	GM19239	blood:	n/a
6	chr5:147443252-147443302	MCF-7	breast:	n/a
7	chr5:147443536-147443586	T-47D	breast:	n/a
8	chr5:147443536-147443586	GM12892	blood:	n/a
9	chr5:147443347-147443397	HCF	heart:	n/a
10	chr5:147443067-147443117	HNPCEpiC	eye:	n/a
11	chr5:147443067-147443117	HRPEpiC	eye:	n/a
12	chr5:147443284-147443334	HRPEpiC	eye:	n/a
13	chr5:147443347-147443397	HRE	kidney:	n/a
14	chr5:147443284-147443334	SK-N-SH_RA	brain:	n/a
15	chr5:147443536-147443586	ProgFib	skin:	n/a
16	chr5:147443284-147443334	HMEC	breast:	n/a
17	chr5:147443347-147443397	PFSK-1	brain:	n/a
18	chr5:147443252-147443302	AG04449	skin:	fetal
19	chr5:147443536-147443586	NH-A	brain:	n/a
20	chr5:147443252-147443302	ECC-1	luminal epithelium:	n/a
21	chr5:147443067-147443117	Caco-2	colon:	n/a
22	chr5:147443284-147443334	HCT-116	colon:	n/a
23	chr5:147443284-147443334	HRE	kidney:	n/a
24	chr5:147443347-147443397	HepG2	liver:	n/a
25	chr5:147443347-147443397	HNPCEpiC	eye:	n/a
26	chr5:147443536-147443586	NB4	blood:	n/a
27	chr5:147443284-147443334	PrEC	prostate:	n/a
28	chr5:147443347-147443397	SK-N-MC	brain:	n/a
29	chr5:147443252-147443302	PFSK-1	brain:	n/a
30	chr5:147443347-147443397	HL-60	blood:	n/a
31	chr5:147443252-147443302	HEK293	kidney:	embryo
32	chr5:147443536-147443586	HUVEC	blood vessel:	n/a
33	chr5:147443347-147443397	K562	blood:	n/a
34	chr5:147443284-147443334	GM12892	blood:	n/a
35	chr5:147443536-147443586	HCM	heart:	n/a
36	chr5:147443536-147443586	AG10803	skin:	n/a
37	chr5:147443252-147443302	SK-N-SH	brain:	n/a
38	chr5:147443284-147443334	SK-N-SH	brain:	n/a
39	chr5:147443252-147443302	HCF	heart:	n/a
40	chr5:147443252-147443302	AG04450	lung:	fetal
41	chr5:147443536-147443586	RPTEC	kidney:	n/a
42	chr5:147443252-147443302	NB4	blood:	n/a
43	chr5:147443067-147443117	PANC-1	pancreas:	n/a
44	chr5:147443252-147443302	HepG2	liver:	n/a
45	chr5:147443536-147443586	Hela-S3	cervix:	n/a
46	chr5:147443284-147443334	NT2-D1	testis:	n/a
47	chr5:147443536-147443586	NHBE	bronchial:	n/a
48	chr5:147443347-147443397	NB4	blood:	n/a
49	chr5:147443252-147443302	HUVEC	blood vessel:	n/a
50	chr5:147443252-147443302	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:147449509..147451055-chr5:147462616..147464573,2	K562	blood:

Variant related genes	Relation type
SPINK5	TF binding region
SPINK5	CpG island

Extended variants
information (count: 527 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:527 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12521791	chr5:147442199-147442200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140230988	chr5:147442210-147442211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150318096	chr5:147442274-147442275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541062114	chr5:147442282-147442283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs137926652	chr5:147442311-147442312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114697189	chr5:147442328-147442329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374496568	chr5:147442363-147442364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566497827	chr5:147442379-147442380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563162492	chr5:147442386-147442387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs3822744	chr5:147442419-147442420	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs548872237	chr5:147442431-147442432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570683407	chr5:147442434-147442435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534609684	chr5:147442493-147442494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546999432	chr5:147442528-147442529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192222182	chr5:147442534-147442535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199645225	chr5:147442553-147442554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539149849	chr5:147442620-147442621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560895830	chr5:147442639-147442640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557463371	chr5:147442686-147442687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149023598	chr5:147442704-147442705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536802786	chr5:147442705-147442706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146906352	chr5:147442735-147442736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs3756688	chr5:147442779-147442780	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs573530503	chr5:147442829-147442830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370779830	chr5:147442848-147442849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3834267	chr5:147442849-147442850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375189968	chr5:147442850-147442851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183821034	chr5:147442864-147442865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1423007	chr5:147442868-147442869	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs139295237	chr5:147442885-147442886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544704630	chr5:147442949-147442950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531923375	chr5:147442963-147442964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143310553	chr5:147442979-147442980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79977837	chr5:147443021-147443022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77190889	chr5:147443055-147443056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112464439	chr5:147443121-147443122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548812741	chr5:147443146-147443147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560897119	chr5:147443165-147443166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528419581	chr5:147443232-147443233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147099496	chr5:147443285-147443286	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs571638346	chr5:147443310-147443311	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs538988568	chr5:147443333-147443334	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs77532553	chr5:147443337-147443338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370073332	chr5:147443348-147443349	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs2287774	chr5:147443360-147443361	Weak transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs536743284	chr5:147443402-147443403	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs116458106	chr5:147443417-147443418	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs2287773	chr5:147443443-147443444	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534524887	chr5:147443452-147443453	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs558936827	chr5:147443532-147443533	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Hyperekplexia	16941485	CNVD
Myelofibrosis	22110671	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147437200-147457400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:147437800-147450200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:147437800-147463800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:147440400-147449600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:147440400-147452800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:147441000-147443200	Weak transcription	NHEK	skin
7	chr5:147441000-147443600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:147442200-147443600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr5:147443200-147444400	Enhancers	NHEK	skin
10	chr5:147443400-147443600	Active TSS	Esophagus	oesophagus
11	chr5:147443600-147443800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:147443600-147443800	Flanking Active TSS	Esophagus	oesophagus
13	chr5:147443600-147444600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr5:147443600-147450000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:147443800-147455400	Weak transcription	Esophagus	oesophagus
16	chr5:147444200-147450400	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr5:147444400-147446400	Weak transcription	NHEK	skin
18	chr5:147444600-147445800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr5:147445800-147449800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr5:147446600-147447000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr5:147447000-147450200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr5:147448200-147450000	Weak transcription	NHEK	skin
23	chr5:147449000-147449200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:147449200-147450200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr5:147449600-147451000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:147449800-147453000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr5:147450000-147450800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr5:147450000-147450800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:147450000-147453000	Enhancers	NHEK	skin
30	chr5:147450200-147450600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr5:147450200-147450800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr5:147450200-147451000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:147450400-147450600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr5:147450400-147450800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr5:147450400-147450800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:147450400-147450800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr5:147450400-147452800	Enhancers	HMEC	breast
38	chr5:147450400-147469000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:147450600-147468600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr5:147450800-147451200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:147450800-147451800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr5:147450800-147474000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr5:147451000-147451400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr5:147451000-147470000	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr5:147451200-147452800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:147451400-147452000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr5:147451800-147452000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr5:147452000-147452400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:147452400-147453200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:147452800-147453600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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