Variant report

Variant	esv2763455
Chromosome Location	chr2:40416373-40433420
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	chr2:40419954-40420391	MCF-7	breast:	n/a	n/a
2	CEBPB	chr2:40419947-40420519	MCF-7	breast:	n/a	n/a
3	CEBPB	chr2:40419972-40420423	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr2:40419994-40420352	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:40420016-40420342	A549	lung:	n/a	n/a
6	CEBPB	chr2:40420027-40420346	HepG2	liver:	n/a	n/a
7	CEBPB	chr2:40420145-40420217	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr2:40424360-40424510	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr2:40424400-40424550	BE2_C	brain:	n/a	n/a
10	CTCF	chr2:40424320-40424470	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr2:40424400-40424550	AG04449	skin:	n/a	n/a
12	CTCF	chr2:40424360-40424510	WERI-Rb-1	eye:	n/a	n/a
13	E2F4	chr2:40419423-40419589	MCF10A-Er-Src	breast:	n/a	n/a
14	EP300	chr2:40426723-40427222	SK-N-SH_RA	brain:	n/a	n/a
15	EP300	chr2:40430242-40430563	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr2:40426667-40427326	SK-N-SH	brain:	n/a	n/a
17	EP300	chr2:40430237-40430579	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr2:40420032-40420554	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr2:40426673-40427362	SK-N-SH	brain:	n/a	n/a
20	EP300	chr2:40426697-40427312	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr2:40431456-40431846	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr2:40424260-40424645	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr2:40419958-40420541	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr2:40424189-40424750	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr2:40420053-40420374	Hela-S3	cervix:	n/a	n/a
26	EP300	chr2:40431392-40431825	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr2:40430164-40430773	SK-N-SH	brain:	n/a	n/a
28	EP300	chr2:40425627-40427323	SK-N-SH	brain:	n/a	chr2:40426215-40426223
29	ESR1	chr2:40427413-40427645	T-47D	breast:	n/a	chr2:40427532-40427549 chr2:40427533-40427550
30	FAM48A	chr2:40418825-40419025	GM12878	blood:	n/a	n/a
31	FOS	chr2:40419926-40420476	MCF10A-Er-Src	breast:	n/a	chr2:40420200-40420211
32	FOS	chr2:40419924-40420423	MCF10A-Er-Src	breast:	n/a	chr2:40420200-40420211
33	FOS	chr2:40420013-40420378	MCF10A-Er-Src	breast:	n/a	chr2:40420200-40420211
34	FOS	chr2:40419974-40420456	MCF10A-Er-Src	breast:	n/a	chr2:40420200-40420211
35	GATA2	chr2:40426887-40427095	SH-SY5Y	brain:	n/a	n/a
36	GATA2	chr2:40420475-40421196	SH-SY5Y	brain:	n/a	chr2:40421018-40421031 chr2:40421020-40421028
37	GATA2	chr2:40423549-40425170	SH-SY5Y	brain:	n/a	chr2:40423621-40423631
38	GATA3	chr2:40426613-40427366	SK-N-SH	brain:	n/a	chr2:40427113-40427120
39	GATA3	chr2:40419996-40420624	MCF-7	breast:	n/a	chr2:40420290-40420298 chr2:40420282-40420290
40	GATA3	chr2:40428605-40428705	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr2:40420080-40420087	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr2:40424079-40424602	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr2:40419968-40421347	SK-N-SH	brain:	n/a	chr2:40420290-40420298 chr2:40421018-40421031 chr2:40421020-40421028 chr2:40420282-40420290
44	GATA3	chr2:40422505-40422683	SH-SY5Y	brain:	n/a	chr2:40422607-40422617
45	GATA3	chr2:40420639-40421260	MCF-7	breast:	n/a	chr2:40421018-40421031 chr2:40421020-40421028
46	GATA3	chr2:40419813-40420725	MCF-7	breast:	n/a	chr2:40420290-40420298 chr2:40420282-40420290
47	GATA3	chr2:40424825-40425022	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr2:40420732-40421181	SH-SY5Y	brain:	n/a	chr2:40421018-40421031 chr2:40421020-40421028
49	GATA3	chr2:40426532-40427341	SK-N-SH	brain:	n/a	chr2:40427113-40427120
50	GATA3	chr2:40430043-40430769	SK-N-SH	brain:	n/a	chr2:40430505-40430516

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:40429179-40429229	HRCEpiC	kidney:	n/a
2	chr2:40429179-40429229	HAEpiC	amniotic membrane:	n/a
3	chr2:40429179-40429229	AG04449	skin:	fetal
4	chr2:40429179-40429229	NHDF-neo	bronchial:	n/a
5	chr2:40429179-40429229	HepG2	liver:	n/a
6	chr2:40429179-40429229	HCF	heart:	n/a
7	chr2:40429179-40429229	SAEC	small airway:	n/a
8	chr2:40429179-40429229	HIPEpiC	eye:	n/a
9	chr2:40429179-40429229	IMR90	lung:	fetal
10	chr2:40429179-40429229	AG10803	skin:	n/a
11	chr2:40429179-40429229	GM06990	blood:	n/a
12	chr2:40429179-40429229	HCM	heart:	n/a
13	chr2:40429179-40429229	Hela-S3	cervix:	n/a
14	chr2:40429179-40429229	PrEC	prostate:	n/a
15	chr2:40429179-40429229	HMEC	breast:	n/a
16	chr2:40429179-40429229	LNCaP	prostate:	n/a
17	chr2:40429179-40429229	ECC-1	luminal epithelium:	n/a
18	chr2:40429179-40429229	A549	lung:	n/a
19	chr2:40429179-40429229	BJ	skin:	n/a
20	chr2:40429179-40429229	K562	blood:	n/a
21	chr2:40429179-40429229	AG04450	lung:	fetal
22	chr2:40429179-40429229	ovcar-3	ovarian:	n/a
23	chr2:40429179-40429229	SKMC	muscle:	n/a
24	chr2:40429179-40429229	NH-A	brain:	n/a
25	chr2:40429179-40429229	BE2_C	brain:	n/a
26	chr2:40429179-40429229	GM12892	blood:	n/a
27	chr2:40429179-40429229	Hepatocyte	liver:	n/a
28	chr2:40429179-40429229	HRPEpiC	eye:	n/a
29	chr2:40429179-40429229	HEK293	kidney:	embryo
30	chr2:40429179-40429229	PANC-1	pancreas:	n/a
31	chr2:40429179-40429229	HEEpiC	esophagus:	n/a
32	chr2:40429179-40429229	HCPEpiC	choroid plexus:	n/a
33	chr2:40429179-40429229	PFSK-1	brain:	n/a
34	chr2:40429179-40429229	HRE	kidney:	n/a
35	chr2:40429179-40429229	HNPCEpiC	eye:	n/a
36	chr2:40429179-40429229	MCF10A-Er-Src	breast:	n/a
37	chr2:40429179-40429229	SK-N-SH_RA	brain:	n/a
38	chr2:40429179-40429229	SK-N-SH	brain:	n/a
39	chr2:40429179-40429229	NT2-D1	testis:	n/a
40	chr2:40429179-40429229	ProgFib	skin:	n/a
41	chr2:40429179-40429229	U87	brain:	n/a
42	chr2:40429179-40429229	GM12891	blood:	n/a
43	chr2:40429179-40429229	HPAEpiC	pulmonary alveolar:	n/a
44	chr2:40429179-40429229	CMK	blood:	n/a
45	chr2:40429179-40429229	MCF-7	breast:	n/a
46	chr2:40429179-40429229	T-47D	breast:	n/a
47	chr2:40429179-40429229	AG09319	gingival:	n/a
48	chr2:40429179-40429229	GM12878	blood:	n/a
49	chr2:40429179-40429229	NB4	blood:	n/a
50	chr2:40429179-40429229	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:40427590..40429513-chr2:40436431..40438074,2	MCF-7	breast:
2	chr2:40430449..40432032-chr2:40434397..40435947,2	K562	blood:
3	chr2:40419927..40421772-chr2:40425195..40428157,2	MCF-7	breast:
4	chr2:40419927..40421772-chr2:40425195..40428157,2	MCF-7	breast:

Variant related genes	Relation type
SLC8A1-AS1	TF binding region
SLC8A1-AS1	CpG island
ENSG00000227028	chromatin interactions

Extended variants
information (count: 723 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2041827	chr2:40416373-40416374	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372119663	chr2:40416378-40416379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374605423	chr2:40416386-40416387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550844872	chr2:40416404-40416405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190179582	chr2:40416478-40416479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536054892	chr2:40416483-40416484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183375143	chr2:40416484-40416485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374711	chr2:40416499-40416500	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs188307488	chr2:40416524-40416525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs193194178	chr2:40416525-40416526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576809209	chr2:40416526-40416527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544148432	chr2:40416530-40416531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140461060	chr2:40416538-40416539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574550615	chr2:40416553-40416554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185538661	chr2:40416608-40416609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554158151	chr2:40416615-40416616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528681706	chr2:40416616-40416617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547020896	chr2:40416621-40416622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565571500	chr2:40416661-40416662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532408605	chr2:40416680-40416681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2041826	chr2:40416684-40416685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577348292	chr2:40416702-40416703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541373572	chr2:40416707-40416708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191262769	chr2:40416761-40416762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183855470	chr2:40416774-40416775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369150112	chr2:40416778-40416779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2033230	chr2:40416805-40416806	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs570685586	chr2:40416808-40416809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574104355	chr2:40416894-40416895	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs389109	chr2:40416919-40416920	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs556097495	chr2:40416930-40416931	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574464644	chr2:40416944-40416945	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs412893	chr2:40416989-40416990	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs10490207	chr2:40417012-40417013	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs181203148	chr2:40417049-40417050	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2033231	chr2:40417099-40417100	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs574500266	chr2:40417105-40417106	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62148765	chr2:40417113-40417114	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs562574842	chr2:40417185-40417186	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189955408	chr2:40417189-40417190	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548321725	chr2:40417225-40417226	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142829313	chr2:40417228-40417229	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13384452	chr2:40417374-40417375	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114021911	chr2:40417471-40417472	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570677341	chr2:40417486-40417487	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538169664	chr2:40417495-40417496	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546923830	chr2:40417551-40417552	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182194387	chr2:40417555-40417556	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374000965	chr2:40417567-40417568	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568312506	chr2:40417571-40417572	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40393000-40420000	Weak transcription	Fetal Kidney	kidney
2	chr2:40393600-40416800	Weak transcription	Fetal Stomach	stomach
3	chr2:40400600-40426800	Weak transcription	Osteobl	bone
4	chr2:40405400-40430000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr2:40405600-40421800	Weak transcription	Right Ventricle	heart
6	chr2:40406400-40416600	Weak transcription	Fetal Muscle Leg	muscle
7	chr2:40406600-40416800	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr2:40407200-40419800	Weak transcription	HSMM	muscle
9	chr2:40411000-40424200	Weak transcription	HSMMtube	muscle
10	chr2:40412000-40421800	Weak transcription	Left Ventricle	heart
11	chr2:40413400-40417800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr2:40413400-40418000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr2:40414800-40417400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr2:40415400-40418800	Enhancers	Fetal Heart	heart
15	chr2:40415600-40416400	Enhancers	Colon Smooth Muscle	Colon
16	chr2:40416000-40425800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr2:40416400-40417400	Weak transcription	Colon Smooth Muscle	Colon
18	chr2:40416600-40417400	Enhancers	Fetal Muscle Leg	muscle
19	chr2:40416800-40418200	Enhancers	Fetal Stomach	stomach
20	chr2:40416800-40418200	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr2:40417200-40430400	Weak transcription	Aorta	Aorta
22	chr2:40417400-40417800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr2:40417400-40417800	Enhancers	Colon Smooth Muscle	Colon
24	chr2:40417400-40418000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr2:40417800-40418000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr2:40417800-40419200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:40417800-40424200	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr2:40417800-40424400	Weak transcription	Colon Smooth Muscle	Colon
29	chr2:40418000-40418200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr2:40418000-40418400	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr2:40418000-40418800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:40418200-40420000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr2:40418200-40447200	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr2:40418400-40420400	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr2:40418600-40445800	Weak transcription	Dnd41	blood
36	chr2:40418800-40419000	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr2:40418800-40420200	Weak transcription	Fetal Heart	heart
38	chr2:40419200-40436600	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:40419800-40420400	Enhancers	HSMM	muscle
40	chr2:40420000-40420400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:40420000-40420600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr2:40420000-40420600	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr2:40420000-40420600	Enhancers	NHLF	lung
44	chr2:40420000-40420800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr2:40420000-40420800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr2:40420000-40420800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr2:40420000-40420800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr2:40420000-40420800	Enhancers	HMEC	breast
49	chr2:40420000-40420800	Enhancers	NHEK	skin
50	chr2:40420000-40421000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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