Variant report

Variant	nsv945353
Chromosome Location	chr1:228634866-228638058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F6	chr1:228634610-228635021	H1-hESC	embryonic stem cell:	n/a	n/a
2	EBF1	chr1:228637365-228637759	GM12878	blood:	n/a	chr1:228637544-228637555
3	ESR1	chr1:228636223-228636541	T-47D	breast:	n/a	n/a
4	ESR1	chr1:228636217-228636512	T-47D	breast:	n/a	n/a
5	ESR1	chr1:228636194-228636581	T-47D	breast:	n/a	n/a
6	MAX	chr1:228634473-228634986	H1-hESC	embryonic stem cell:	n/a	n/a
7	MAX	chr1:228634559-228634966	H1-hESC	embryonic stem cell:	n/a	n/a
8	MAX	chr1:228636096-228636289	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr1:228637940-228638218	Hela-S3	cervix:	n/a	n/a
10	RAD21	chr1:228634559-228634898	H1-hESC	embryonic stem cell:	n/a	chr1:228634705-228634717
11	RAD21	chr1:228634578-228634895	H1-hESC	embryonic stem cell:	n/a	chr1:228634705-228634717
12	RAD21	chr1:228634469-228634903	H1-hESC	embryonic stem cell:	n/a	chr1:228634705-228634717
13	RCOR1	chr1:228636921-228637025	K562	blood:	n/a	n/a
14	STAT3	chr1:228635605-228635859	MCF10A-Er-Src	breast:	n/a	n/a
15	USF1	chr1:228636039-228636283	K562	blood:	n/a	n/a
16	USF2	chr1:228636173-228636186	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:228638058-228638108	ovcar-3	ovarian:	n/a
2	chr1:228638058-228638108	HMEC	breast:	n/a
3	chr1:228638058-228638108	HCT-116	colon:	n/a
4	chr1:228638058-228638108	LNCaP	prostate:	n/a
5	chr1:228638058-228638108	HRCEpiC	kidney:	n/a
6	chr1:228638058-228638108	PFSK-1	brain:	n/a
7	chr1:228638058-228638108	HEK293	kidney:	embryo
8	chr1:228638058-228638108	Caco-2	colon:	n/a
9	chr1:228638058-228638108	SK-N-MC	brain:	n/a
10	chr1:228638058-228638108	ECC-1	luminal epithelium:	n/a
11	chr1:228638058-228638108	HEEpiC	esophagus:	n/a
12	chr1:228638058-228638108	A549	lung:	n/a
13	chr1:228638058-228638108	HAEpiC	amniotic membrane:	n/a
14	chr1:228638058-228638108	Hepatocyte	liver:	n/a
15	chr1:228638058-228638108	GM12878	blood:	n/a
16	chr1:228638058-228638108	NHDF-neo	bronchial:	n/a
17	chr1:228638058-228638108	HCM	heart:	n/a
18	chr1:228638058-228638108	CMK	blood:	n/a
19	chr1:228638058-228638108	K562	blood:	n/a
20	chr1:228638058-228638108	IMR90	lung:	fetal
21	chr1:228638058-228638108	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:228638058-228638108	BJ	skin:	n/a
23	chr1:228638058-228638108	NB4	blood:	n/a
24	chr1:228638058-228638108	MCF-7	breast:	n/a
25	chr1:228638058-228638108	MCF10A-Er-Src	breast:	n/a
26	chr1:228638058-228638108	BE2_C	brain:	n/a
27	chr1:228638058-228638108	SK-N-SH	brain:	n/a
28	chr1:228638058-228638108	PrEC	prostate:	n/a
29	chr1:228638058-228638108	HIPEpiC	eye:	n/a
30	chr1:228638058-228638108	HRPEpiC	eye:	n/a
31	chr1:228638058-228638108	SKMC	muscle:	n/a
32	chr1:228638058-228638108	AG09309	skin:	n/a
33	chr1:228638058-228638108	HCPEpiC	choroid plexus:	n/a
34	chr1:228638058-228638108	GM12891	blood:	n/a
35	chr1:228638058-228638108	U87	brain:	n/a
36	chr1:228638058-228638108	ProgFib	skin:	n/a
37	chr1:228638058-228638108	HUVEC	blood vessel:	n/a
38	chr1:228638058-228638108	T-47D	breast:	n/a
39	chr1:228638058-228638108	RPTEC	kidney:	n/a
40	chr1:228638058-228638108	HCF	heart:	n/a
41	chr1:228638058-228638108	AoSMC	blood vessel:	n/a
42	chr1:228638058-228638108	HepG2	liver:	n/a
43	chr1:228638058-228638108	H1-hESC	embryonic stem cell:	embryo
44	chr1:228638058-228638108	HRE	kidney:	n/a
45	chr1:228638058-228638108	NH-A	brain:	n/a
46	chr1:228638058-228638108	GM12892	blood:	n/a
47	chr1:228638058-228638108	AG10803	skin:	n/a
48	chr1:228638058-228638108	GM06990	blood:	n/a
49	chr1:228638058-228638108	PANC-1	pancreas:	n/a
50	chr1:228638058-228638108	HNPCEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:228520549..228522898-chr1:228637916..228639790,2	K562	blood:
2	chr1:228633250..228635645-chr1:228673935..228676432,2	MCF-7	breast:
3	chr1:228526564..228529508-chr1:228637709..228639977,2	K562	blood:
4	chr1:228554896..228558917-chr1:228634186..228636261,3	K562	blood:
5	chr1:228594178..228596096-chr1:228634719..228637473,2	MCF-7	breast:
6	chr1:228627994..228630263-chr1:228633987..228636188,2	MCF-7	breast:
7	chr1:228635449..228637961-chr12:122750153..122751748,2	MCF-7	breast:
8	chr1:228635196..228636992-chr1:228643144..228645156,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000230841	TF binding region
ENSG00000230841	CpG island
ENSG00000256861	chromatin interactions
ENSG00000168159	chromatin interactions
ENSG00000154370	chromatin interactions
ENSG00000231563	chromatin interactions
ENSG00000139719	chromatin interactions
ENSG00000154358	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376643986	chr1:228634879-228634880	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs10916316	chr1:228634917-228634918	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs557033985	chr1:228634924-228634925	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs113083459	chr1:228634975-228634976	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs371752763	chr1:228635003-228635004	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs150656455	chr1:228635012-228635013	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs114503234	chr1:228635060-228635061	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs573403887	chr1:228635072-228635073	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs551288507	chr1:228635102-228635103	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs539537313	chr1:228635117-228635118	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs542132810	chr1:228635136-228635137	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs562400057	chr1:228635199-228635200	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs372277956	chr1:228635256-228635257	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs543488937	chr1:228635258-228635259	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs79053777	chr1:228635314-228635315	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs571159987	chr1:228635328-228635329	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs367643637	chr1:228635345-228635346	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs115164365	chr1:228635433-228635434	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs115557820	chr1:228635443-228635444	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs187444928	chr1:228635485-228635486	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs543697595	chr1:228635512-228635513	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs193263234	chr1:228635573-228635574	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs369376426	chr1:228635615-228635616	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs553565133	chr1:228635732-228635733	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs373521797	chr1:228635789-228635790	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs548072057	chr1:228635971-228635972	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs568061432	chr1:228635973-228635974	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs536953197	chr1:228636000-228636001	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs550524048	chr1:228636037-228636038	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs185421336	chr1:228636039-228636040	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs144026488	chr1:228636118-228636119	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs539517494	chr1:228636171-228636172	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs553457778	chr1:228636219-228636220	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs116725414	chr1:228636249-228636250	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs114364193	chr1:228636250-228636251	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs556091953	chr1:228636289-228636290	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs145944786	chr1:228636315-228636316	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs115984883	chr1:228636354-228636355	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs563240164	chr1:228636380-228636381	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs116960142	chr1:228636391-228636392	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs78425551	chr1:228636398-228636399	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs111738526	chr1:228636413-228636414	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs190324915	chr1:228636443-228636444	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs181629307	chr1:228636464-228636465	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs561557837	chr1:228636481-228636482	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs530684782	chr1:228636495-228636496	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs550485673	chr1:228636528-228636529	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs138324369	chr1:228636538-228636539	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs570731483	chr1:228636561-228636562	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs555492922	chr1:228636640-228636641	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228633200-228635000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr1:228633400-228635000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
3	chr1:228633600-228635000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
4	chr1:228633600-228635000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
5	chr1:228633800-228635000	Enhancers	Fetal Brain Male	brain
6	chr1:228633800-228636000	Weak transcription	K562	blood
7	chr1:228634000-228643200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr1:228634200-228635000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:228634200-228641600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr1:228634200-228643000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:228634200-228644800	Weak transcription	Gastric	stomach
12	chr1:228634400-228635000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:228634400-228635000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:228634400-228638000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:228634400-228641600	Weak transcription	Brain Angular Gyrus	brain
16	chr1:228634400-228644200	Weak transcription	Brain Anterior Caudate	brain
17	chr1:228634400-228644600	Weak transcription	Right Atrium	heart
18	chr1:228634400-228644600	Weak transcription	Right Ventricle	heart
19	chr1:228634600-228635000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
20	chr1:228634800-228635000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
21	chr1:228634800-228635000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:228634800-228635000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
23	chr1:228634800-228635000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
24	chr1:228634800-228635000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:228634800-228635000	Enhancers	Brain Germinal Matrix	brain
26	chr1:228634800-228635200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:228635000-228635200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:228635000-228639800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr1:228635000-228640200	Weak transcription	Fetal Brain Male	brain
30	chr1:228635000-228640600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:228635000-228641400	Weak transcription	Brain Germinal Matrix	brain
32	chr1:228635000-228641600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:228635000-228642000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr1:228635200-228637200	Enhancers	Placenta	Placenta
35	chr1:228635200-228643000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:228635200-228644200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:228635400-228639200	Weak transcription	Fetal Intestine Small	intestine
38	chr1:228635600-228641400	Weak transcription	Fetal Brain Female	brain
39	chr1:228635800-228643000	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr1:228636000-228638400	Enhancers	K562	blood
41	chr1:228636600-228641200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:228637000-228641600	Weak transcription	Fetal Muscle Leg	muscle
43	chr1:228637200-228640000	Weak transcription	Placenta	Placenta
44	chr1:228637400-228643000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr1:228637600-228643400	Weak transcription	Brain Hippocampus Middle	brain
46	chr1:228638000-228638200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:228638000-228638200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr1:228638000-228643000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links