Variant report

Variant	nsv873863
Chromosome Location	chr2:35909000-36019937
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	chr2:35939861-35940404	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr2:36000765-36000949	A549	lung:	n/a	chr2:36000859-36000870 chr2:36000860-36000871
3	CEBPB	chr2:36000760-36001020	HepG2	liver:	n/a	chr2:36000859-36000870 chr2:36000860-36000871
4	CEBPB	chr2:35933608-35933969	HepG2	liver:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
5	CEBPB	chr2:35966704-35966918	A549	lung:	n/a	n/a
6	CEBPB	chr2:35913520-35913719	A549	lung:	n/a	n/a
7	CEBPB	chr2:35933609-35933948	IMR90	lung:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
8	CEBPB	chr2:35939980-35940327	K562	blood:	n/a	n/a
9	CEBPB	chr2:35923382-35923646	HepG2	liver:	n/a	chr2:35923513-35923522 chr2:35923513-35923524 chr2:35923491-35923502 chr2:35923511-35923522 chr2:35923511-35923524
10	CEBPB	chr2:35966667-35966899	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:36003004-36003201	A549	lung:	n/a	chr2:36003126-36003135 chr2:36003124-36003135 chr2:36003125-36003136
12	CEBPB	chr2:35939944-35940305	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:36000495-36000514	HepG2	liver:	n/a	chr2:36000495-36000506
14	CEBPB	chr2:35933650-35933879	MCF-7	breast:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
15	CEBPB	chr2:36002964-36003212	HepG2	liver:	n/a	chr2:36003126-36003135 chr2:36003124-36003135 chr2:36003125-36003136
16	CEBPB	chr2:35931148-35931461	HepG2	liver:	n/a	chr2:35931306-35931319 chr2:35931306-35931317
17	CEBPB	chr2:35939909-35940320	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:35966616-35966957	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:35939938-35940319	A549	lung:	n/a	n/a
20	CEBPB	chr2:35931181-35931345	H1-hESC	embryonic stem cell:	n/a	chr2:35931306-35931319 chr2:35931306-35931317
21	CEBPB	chr2:35939874-35940327	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:35933609-35933943	H1-hESC	embryonic stem cell:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
23	CEBPB	chr2:35933607-35933953	A549	lung:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
24	CEBPB	chr2:35939882-35940380	A549	lung:	n/a	n/a
25	CEBPB	chr2:36012772-36012798	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:35933490-35933969	Hela-S3	cervix:	n/a	chr2:35933776-35933785 chr2:35933774-35933785 chr2:35933776-35933787
27	CTCF	chr2:36008940-36009090	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr2:36009037-36009131	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr2:36008980-36009130	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr2:36008982-36009138	A549	lung:	n/a	n/a
31	CTCF	chr2:36009040-36009190	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr2:36008960-36009110	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:35933480-35933630	HAc	cerebellar:	n/a	n/a
34	CTCF	chr2:36009018-36009122	ProgFib	skin:	n/a	n/a
35	CTCF	chr2:36008844-36009272	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:36009123-36009124	ProgFib	skin:	n/a	n/a
37	CTCF	chr2:36008917-36009206	A549	lung:	n/a	n/a
38	CTCF	chr2:35930220-35930370	HPF	lung:	n/a	n/a
39	CTCF	chr2:36009015-36009110	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr2:36008960-36009110	A549	lung:	n/a	n/a
41	CTCF	chr2:35956707-35956709	IMR90	lung:	n/a	n/a
42	CTCF	chr2:36008959-36009193	Gliobla	brain:	n/a	n/a
43	CTCF	chr2:36008909-36009146	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr2:36008960-36009110	HMEC	breast:	n/a	n/a
45	CTCF	chr2:36009000-36009150	HepG2	liver:	n/a	n/a
46	CTCF	chr2:36008965-36009180	LNCaP	prostate:	n/a	n/a
47	CTCF	chr2:35951400-35951550	AG10803	skin:	n/a	n/a
48	CTCF	chr2:36009059-36009101	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr2:36009040-36009108	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:35964402-35964423	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36018275-36018325	ovcar-3	ovarian:	n/a
2	chr2:36018275-36018325	AG04449	skin:	fetal
3	chr2:36018275-36018325	BJ	skin:	n/a
4	chr2:36018275-36018325	NT2-D1	testis:	n/a
5	chr2:36018275-36018325	HRCEpiC	kidney:	n/a
6	chr2:36018275-36018325	HL-60	blood:	n/a
7	chr2:36018275-36018325	Caco-2	colon:	n/a
8	chr2:36018275-36018325	Hepatocyte	liver:	n/a
9	chr2:36018275-36018325	HNPCEpiC	eye:	n/a
10	chr2:36018275-36018325	PFSK-1	brain:	n/a
11	chr2:36018275-36018325	A549	lung:	n/a
12	chr2:36018275-36018325	NB4	blood:	n/a
13	chr2:36018275-36018325	HepG2	liver:	n/a
14	chr2:36018275-36018325	SKMC	muscle:	n/a
15	chr2:36018275-36018325	T-47D	breast:	n/a
16	chr2:36018275-36018325	HCT-116	colon:	n/a
17	chr2:36018275-36018325	HEEpiC	esophagus:	n/a
18	chr2:36018275-36018325	NH-A	brain:	n/a
19	chr2:36018275-36018325	ProgFib	skin:	n/a
20	chr2:36018275-36018325	HCF	heart:	n/a
21	chr2:36018275-36018325	ECC-1	luminal epithelium:	n/a
22	chr2:36018275-36018325	AoSMC	blood vessel:	n/a
23	chr2:36018275-36018325	Hela-S3	cervix:	n/a
24	chr2:36018275-36018325	U87	brain:	n/a
25	chr2:36018275-36018325	LNCaP	prostate:	n/a
26	chr2:36018275-36018325	SK-N-SH	brain:	n/a
27	chr2:36018275-36018325	AG09319	gingival:	n/a
28	chr2:36018275-36018325	GM12891	blood:	n/a
29	chr2:36018275-36018325	RPTEC	kidney:	n/a
30	chr2:36018275-36018325	Jurkat	blood:	n/a
31	chr2:36018275-36018325	SK-N-MC	brain:	n/a
32	chr2:36018275-36018325	NHDF-neo	bronchial:	n/a
33	chr2:36018275-36018325	PrEC	prostate:	n/a
34	chr2:36018275-36018325	HMEC	breast:	n/a
35	chr2:36018275-36018325	GM19239	blood:	n/a
36	chr2:36018275-36018325	HRE	kidney:	n/a
37	chr2:36018275-36018325	AG10803	skin:	n/a
38	chr2:36018275-36018325	HIPEpiC	eye:	n/a
39	chr2:36018275-36018325	GM12878	blood:	n/a
40	chr2:36018275-36018325	GM06990	blood:	n/a
41	chr2:36018275-36018325	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:36018275-36018325	AG09309	skin:	n/a
43	chr2:36018275-36018325	HUVEC	blood vessel:	n/a
44	chr2:36018275-36018325	H1-hESC	embryonic stem cell:	embryo
45	chr2:36018275-36018325	BE2_C	brain:	n/a
46	chr2:36018275-36018325	CMK	blood:	n/a
47	chr2:36018275-36018325	GM12892	blood:	n/a
48	chr2:36018275-36018325	AG04450	lung:	fetal
49	chr2:36018275-36018325	PANC-1	pancreas:	n/a
50	chr2:36018275-36018325	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:35949877..35953265-chr2:35954228..35956588,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-6	chr2:35949825-35950208	NONHSAT070075

Variant related genes	Relation type
MRPL50P1	TF binding region
MRPL50P1	CpG island
ENSG00000234587	chromatin interactions

Extended variants
information (count: 2988 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2988 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs925910	chr2:35909000-35909001	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182885185	chr2:35909012-35909013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534400882	chr2:35909054-35909055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559247604	chr2:35909081-35909082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80002082	chr2:35909101-35909102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538245554	chr2:35909153-35909154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187399220	chr2:35909168-35909169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575154557	chr2:35909207-35909208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575050315	chr2:35909240-35909241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191482776	chr2:35909242-35909243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572656851	chr2:35909274-35909275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113153162	chr2:35909281-35909282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114312250	chr2:35909285-35909286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548186775	chr2:35909296-35909297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs925911	chr2:35909305-35909306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367641554	chr2:35909328-35909329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184062936	chr2:35909329-35909330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76922456	chr2:35909330-35909331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530053561	chr2:35909386-35909387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138025873	chr2:35909387-35909388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs59151177	chr2:35909409-35909410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13031628	chr2:35909410-35909411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62145420	chr2:35909414-35909415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62145421	chr2:35909420-35909421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138525303	chr2:35909421-35909422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62145422	chr2:35909424-35909425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs386644802	chr2:35909452-35909453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116420643	chr2:35909453-35909454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564691718	chr2:35909460-35909461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79966112	chr2:35909476-35909477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370065766	chr2:35909478-35909479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192663485	chr2:35909497-35909498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373713885	chr2:35909523-35909524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13031674	chr2:35909530-35909531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs150376242	chr2:35909561-35909562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13032391	chr2:35909573-35909574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs568795648	chr2:35909576-35909577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184461833	chr2:35909621-35909622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190624539	chr2:35909630-35909631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538756512	chr2:35909638-35909639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138109196	chr2:35909682-35909683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13008963	chr2:35909684-35909685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs36113363	chr2:35909725-35909726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs576983968	chr2:35909742-35909743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142544168	chr2:35909791-35909792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562646446	chr2:35909879-35909880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76691450	chr2:35909880-35909881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542289245	chr2:35909885-35909886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371429229	chr2:35909905-35909906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13032733	chr2:35909924-35909925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

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
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	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	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	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
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35902000-35909000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:35908400-35909200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:35908400-35909200	Enhancers	Fetal Intestine Large	intestine
4	chr2:35909000-35909200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr2:35909200-35910800	Weak transcription	Fetal Intestine Large	intestine
6	chr2:35910000-35910200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:35910800-35911000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr2:35910800-35911000	Enhancers	Fetal Intestine Large	intestine
9	chr2:35917800-35918400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:35922800-35923600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:35937200-35955200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:35943200-35943400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:35947200-35947600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr2:35955000-35955800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr2:35955000-35955800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:35955200-35955400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:35955200-35955800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr2:35955200-35955800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:35955400-35955800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr2:35955600-35956000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:35959400-35960000	Enhancers	Fetal Muscle Trunk	muscle
22	chr2:35962600-35963800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr2:35963600-35963800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr2:35963800-35971600	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr2:35963800-35972000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr2:35971600-35972000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:35972000-35972200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr2:35977000-35977200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr2:35977200-35980000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:35980000-35984600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr2:35984600-35985000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:35985000-35986600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr2:35986600-35987000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:35987000-35990600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr2:35990600-35991600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:35997000-36004600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:36004600-36005600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:36005600-36008000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:36008000-36008600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:36008600-36009000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:36008600-36009400	Enhancers	A549	lung
42	chr2:36009000-36009200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:36009200-36011800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:36011800-36016600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:36012000-36012800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:36012200-36013200	Enhancers	HMEC	breast
47	chr2:36012800-36015200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:36013200-36020200	Weak transcription	HMEC	breast
49	chr2:36015200-36015600	Enhancers	Pancreas	Pancrea
50	chr2:36015200-36016000	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links