Variant report

Variant	nsv461205
Chromosome Location	chr4:7434017-7442126
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	BRCA1	chr4:7436571-7436572	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:7437595-7437783	HepG2	liver:	n/a	n/a
3	CEBPB	chr4:7437550-7437908	HepG2	liver:	n/a	n/a
4	CHD2	chr4:7441612-7441614	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr4:7436619-7436861	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr4:7435308-7435402	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr4:7436683-7436741	LNCaP	prostate:	n/a	chr4:7436701-7436719
8	CTCF	chr4:7439780-7439930	HCM	heart:	n/a	n/a
9	CTCF	chr4:7439807-7439863	K562	blood:	n/a	n/a
10	CTCF	chr4:7439840-7439990	BE2_C	brain:	n/a	n/a
11	CTCF	chr4:7439814-7439928	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:7439740-7439890	HCT-116	colon:	n/a	n/a
13	CTCF	chr4:7439967-7439994	Lung_OC	lung:	n/a	n/a
14	CTCF	chr4:7435260-7435410	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr4:7435240-7435390	AG04449	skin:	n/a	n/a
16	CTCF	chr4:7439852-7439886	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:7439843-7439902	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:7439720-7439870	HCT-116	colon:	n/a	n/a
19	CTCF	chr4:7439800-7439950	HBMEC	blood vessel:	n/a	n/a
20	E2F4	chr4:7436626-7436856	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr4:7436597-7436862	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
22	FOS	chr4:7436578-7436862	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
23	FOS	chr4:7436572-7436866	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
24	FOS	chr4:7436573-7436878	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
25	FOSL2	chr4:7436508-7436891	HepG2	liver:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
26	FOXA2	chr4:7437238-7437500	HepG2	liver:	n/a	n/a
27	IRF1	chr4:7440219-7440283	K562	blood:	n/a	n/a
28	JUND	chr4:7436652-7436849	K562	blood:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
29	JUND	chr4:7436609-7436834	HepG2	liver:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
30	JUND	chr4:7436635-7436850	H1-hESC	embryonic stem cell:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
31	JUND	chr4:7436533-7436871	A549	lung:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
32	JUND	chr4:7436677-7436865	HepG2	liver:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
33	JUND	chr4:7441458-7441635	HepG2	liver:	n/a	n/a
34	KAP1	chr4:7436633-7436966	U2OS	brain:	n/a	n/a
35	MAZ	chr4:7436590-7436813	Hela-S3	cervix:	n/a	n/a
36	MAZ	chr4:7436715-7436887	HepG2	liver:	n/a	n/a
37	MAZ	chr4:7437184-7437199	HepG2	liver:	n/a	n/a
38	POLR2A	chr4:7440146-7440312	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr4:7435661-7435688	MCF-7	breast:	n/a	n/a
40	POLR2A	chr4:7436568-7436901	HCT-116	colon:	n/a	n/a
41	RAD21	chr4:7436604-7436836	H1-hESC	embryonic stem cell:	n/a	chr4:7436699-7436718 chr4:7436703-7436717
42	RAD21	chr4:7436693-7436806	Hela-S3	cervix:	n/a	chr4:7436699-7436718 chr4:7436703-7436717
43	RCOR1	chr4:7436669-7436869	Hela-S3	cervix:	n/a	n/a
44	RFX5	chr4:7436603-7436809	Hela-S3	cervix:	n/a	n/a
45	SETDB1	chr4:7440641-7441113	U2OS	brain:	n/a	n/a
46	SMC3	chr4:7436623-7436854	Hela-S3	cervix:	n/a	n/a
47	STAT3	chr4:7436656-7436857	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr4:7436640-7436858	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr4:7435850-7436030	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7436874-7436924	SK-N-MC	brain:	n/a
2	chr4:7435463-7435513	GM12891	blood:	n/a
3	chr4:7434754-7434804	PFSK-1	brain:	n/a
4	chr4:7438613-7438663	PrEC	prostate:	n/a
5	chr4:7438613-7438663	HCF	heart:	n/a
6	chr4:7435639-7435689	HRCEpiC	kidney:	n/a
7	chr4:7436861-7436911	HNPCEpiC	eye:	n/a
8	chr4:7436199-7436249	AG09319	gingival:	n/a
9	chr4:7437156-7437206	GM19239	blood:	n/a
10	chr4:7436693-7436743	MCF10A-Er-Src	breast:	n/a
11	chr4:7438613-7438663	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:7435357-7435407	H1-hESC	embryonic stem cell:	embryo
13	chr4:7436861-7436911	BE2_C	brain:	n/a
14	chr4:7436701-7436751	IMR90	lung:	fetal
15	chr4:7435357-7435407	HRE	kidney:	n/a
16	chr4:7436693-7436743	SK-N-MC	brain:	n/a
17	chr4:7435357-7435407	HCF	heart:	n/a
18	chr4:7436199-7436249	AG04450	lung:	fetal
19	chr4:7437027-7437077	NHBE	bronchial:	n/a
20	chr4:7436701-7436751	HIPEpiC	eye:	n/a
21	chr4:7436259-7436309	RPTEC	kidney:	n/a
22	chr4:7436874-7436924	HCM	heart:	n/a
23	chr4:7436199-7436249	PANC-1	pancreas:	n/a
24	chr4:7438657-7438707	GM12891	blood:	n/a
25	chr4:7434754-7434804	HUVEC	blood vessel:	n/a
26	chr4:7436701-7436751	Hepatocyte	liver:	n/a
27	chr4:7438613-7438663	MCF10A-Er-Src	breast:	n/a
28	chr4:7437812-7437862	ECC-1	luminal epithelium:	n/a
29	chr4:7437812-7437862	SK-N-MC	brain:	n/a
30	chr4:7435639-7435689	GM19239	blood:	n/a
31	chr4:7436874-7436924	MCF10A-Er-Src	breast:	n/a
32	chr4:7437027-7437077	HEK293	kidney:	embryo
33	chr4:7438613-7438663	GM12878	blood:	n/a
34	chr4:7438657-7438707	GM12878	blood:	n/a
35	chr4:7436861-7436911	AG10803	skin:	n/a
36	chr4:7436693-7436743	K562	blood:	n/a
37	chr4:7435357-7435407	AG04450	lung:	fetal
38	chr4:7436874-7436924	AG04449	skin:	fetal
39	chr4:7436701-7436751	RPTEC	kidney:	n/a
40	chr4:7436874-7436924	HUVEC	blood vessel:	n/a
41	chr4:7436701-7436751	HEK293	kidney:	embryo
42	chr4:7436199-7436249	HCT-116	colon:	n/a
43	chr4:7436199-7436249	GM12878	blood:	n/a
44	chr4:7435357-7435407	Hepatocyte	liver:	n/a
45	chr4:7438657-7438707	GM06990	blood:	n/a
46	chr4:7438657-7438707	T-47D	breast:	n/a
47	chr4:7436861-7436911	MCF10A-Er-Src	breast:	n/a
48	chr4:7436874-7436924	MCF-7	breast:	n/a
49	chr4:7436693-7436743	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:7435357-7435407	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr4:7421765..7423604-chr4:7439157..7441831,2	K562	blood:
2	chr4:7436453..7438238-chr4:7441242..7443096,2	MCF-7	breast:
3	chr4:7426666..7428188-chr4:7440042..7442576,2	MCF-7	breast:
4	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
5	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:

Variant related genes	Relation type
PSAPL1	TF binding region
PSAPL1	CpG island
ENSG00000178597	chromatin interactions

Extended variants
information (count: 545 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:545 , 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	rs10033032	chr4:7434017-7434018	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530853986	chr4:7434021-7434022	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs569176151	chr4:7434051-7434052	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs73796584	chr4:7434063-7434064	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs181923378	chr4:7434098-7434099	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs138981228	chr4:7434122-7434123	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs547162839	chr4:7434194-7434195	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs57186692	chr4:7434202-7434203	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs529498604	chr4:7434211-7434212	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs551171931	chr4:7434221-7434222	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs569326387	chr4:7434222-7434223	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs60545072	chr4:7434257-7434258	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558939582	chr4:7434270-7434271	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs367631628	chr4:7434271-7434272	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs534294548	chr4:7434280-7434281	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs149393116	chr4:7434305-7434306	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs554159392	chr4:7434316-7434317	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs114948233	chr4:7434324-7434325	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs553074099	chr4:7434362-7434363	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531101006	chr4:7434367-7434368	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs535173166	chr4:7434410-7434411	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs72355702	chr4:7434412-7434413	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs557121211	chr4:7434413-7434414	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs201230051	chr4:7434414-7434415	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs371579178	chr4:7434415-7434416	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs369263860	chr4:7434416-7434417	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs540617146	chr4:7434446-7434447	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs10023470	chr4:7434456-7434457	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs529413727	chr4:7434479-7434480	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs550752770	chr4:7434554-7434555	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs563108370	chr4:7434563-7434564	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs77691359	chr4:7434579-7434580	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs386399176	chr4:7434580-7434581	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs575921833	chr4:7434584-7434585	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs187263618	chr4:7434594-7434595	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs10014338	chr4:7434607-7434608	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs534186864	chr4:7434652-7434653	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189186171	chr4:7434653-7434654	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs553453784	chr4:7434658-7434659	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148422088	chr4:7434661-7434662	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs115136197	chr4:7434669-7434670	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs556771523	chr4:7434688-7434689	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs180721983	chr4:7434706-7434707	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs539235359	chr4:7434726-7434727	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs143502297	chr4:7434727-7434728	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs573191781	chr4:7434744-7434745	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs540507153	chr4:7434754-7434755	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs562069194	chr4:7434763-7434764	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs573914149	chr4:7434765-7434766	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs7439798	chr4:7434780-7434781	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7423200-7436200	Weak transcription	Right Atrium	heart
2	chr4:7427000-7438800	Weak transcription	Spleen	Spleen
3	chr4:7431800-7436400	Weak transcription	Left Ventricle	heart
4	chr4:7431800-7436400	Weak transcription	Right Ventricle	heart
5	chr4:7432000-7436400	Weak transcription	Fetal Heart	heart
6	chr4:7432200-7436400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:7432400-7436400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:7432600-7436200	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr4:7432600-7436400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:7432600-7436400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:7432800-7437000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:7433000-7436000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:7433000-7436400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:7433000-7436400	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr4:7433000-7437600	Weak transcription	Lung	lung
16	chr4:7433600-7435800	Flanking Active TSS	Stomach Mucosa	stomach
17	chr4:7433800-7436200	Weak transcription	Fetal Intestine Small	intestine
18	chr4:7433800-7436400	Weak transcription	Esophagus	oesophagus
19	chr4:7433800-7436400	Weak transcription	A549	lung
20	chr4:7433800-7436400	Weak transcription	HMEC	breast
21	chr4:7433800-7436800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:7434000-7436000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:7434600-7436000	Active TSS	Gastric	stomach
24	chr4:7435800-7436400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
25	chr4:7435800-7440200	Enhancers	Stomach Mucosa	stomach
26	chr4:7436000-7438200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:7436000-7438400	Enhancers	Gastric	stomach
28	chr4:7436200-7436400	Enhancers	Right Atrium	heart
29	chr4:7436200-7438000	Enhancers	Placenta Amnion	Placenta Amnion
30	chr4:7436200-7439600	Enhancers	Fetal Intestine Large	intestine
31	chr4:7436200-7439600	Enhancers	Fetal Intestine Small	intestine
32	chr4:7436400-7436600	Enhancers	HepG2	liver
33	chr4:7436400-7436800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:7436400-7437000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:7436400-7437000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr4:7436400-7437000	Bivalent Enhancer	Fetal Stomach	stomach
37	chr4:7436400-7437000	Weak transcription	Right Atrium	heart
38	chr4:7436400-7437000	Enhancers	NHEK	skin
39	chr4:7436400-7437200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr4:7436400-7437200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:7436400-7437200	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:7436400-7437200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:7436400-7437200	Enhancers	Fetal Heart	heart
44	chr4:7436400-7437200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr4:7436400-7437200	Bivalent Enhancer	Fetal Muscle Leg	muscle
46	chr4:7436400-7437200	Enhancers	Left Ventricle	heart
47	chr4:7436400-7437200	Enhancers	Right Ventricle	heart
48	chr4:7436400-7437200	Enhancers	A549	lung
49	chr4:7436400-7437200	Enhancers	HMEC	breast
50	chr4:7436400-7437800	Enhancers	Esophagus	oesophagus

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