Variant report

Variant	nsv1059551
Chromosome Location	chr20:52644770-52658639
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr20:52652599-52652817	A549	lung:	n/a	chr20:52652797-52652809
2	CTCF	chr20:52656980-52657130	NHDF-neo	bronchial:	n/a	n/a
3	CTCF	chr20:52644932-52644961	ProgFib	skin:	n/a	n/a
4	CTCF	chr20:52649892-52649926	Lung_OC	lung:	n/a	n/a
5	CTCF	chr20:52644962-52644976	ProgFib	skin:	n/a	n/a
6	GATA3	chr20:52646629-52646974	SH-SY5Y	brain:	n/a	n/a
7	GTF2F1	chr20:52655601-52655670	K562	blood:	n/a	n/a
8	MYC	chr20:52644910-52644973	H1-hESC	embryonic stem cell:	n/a	n/a
9	MYC	chr20:52655714-52655734	K562	blood:	n/a	n/a
10	POLR2A	chr20:52644898-52645206	ProgFib	skin:	n/a	n/a
11	POLR2A	chr20:52645224-52645292	ProgFib	skin:	n/a	n/a
12	POLR2A	chr20:52646455-52646601	ProgFib	skin:	n/a	n/a
13	POLR2A	chr20:52644817-52644821	ProgFib	skin:	n/a	n/a
14	POLR2A	chr20:52656922-52656928	ProgFib	skin:	n/a	n/a
15	POLR2A	chr20:52644891-52645058	A549	lung:	n/a	n/a
16	RCOR1	chr20:52654183-52654358	K562	blood:	n/a	n/a
17	RCOR1	chr20:52654150-52654334	K562	blood:	n/a	n/a
18	SPI1	chr20:52657027-52657212	K562	blood:	n/a	n/a
19	USF2	chr20:52644979-52644984	H1-hESC	embryonic stem cell:	n/a	n/a
20	ZNF384	chr20:52658357-52658546	K562	blood:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:52640367..52641889-chr20:52645625..52647973,2	K562	blood:
2	chr20:52643210..52646138-chr20:52658422..52660423,2	K562	blood:
3	chr20:52646106..52649105-chr20:52656818..52659729,2	MCF-7	breast:
4	chr17:57915947..57917652-chr20:52646723..52649567,2	MCF-7	breast:
5	chr20:52637408..52640155-chr20:52655059..52656752,2	MCF-7	breast:
6	chr17:57917278..57919596-chr20:52653625..52656516,2	MCF-7	breast:
7	chr20:52626505..52628533-chr20:52652801..52654568,2	MCF-7	breast:
8	chr20:52643673..52645639-chr20:52687051..52688962,2	MCF-7	breast:
9	chr2:99769202..99772000-chr20:52646224..52647934,2	MCF-7	breast:
10	chr17:56707799..56710607-chr20:52642228..52644941,3	MCF-7	breast:
11	chr20:52642833..52647245-chr20:52651317..52656592,5	MCF-7	breast:
12	chr20:52557746..52563146-chr20:52657006..52659772,4	MCF-7	breast:
13	chr20:52648757..52649473-chr5:157170244..157171208,2	MCF-7	breast:
14	chr20:52647368..52649299-chr20:52654193..52656329,2	MCF-7	breast:
15	chr19:11025812..11027987-chr20:52653374..52655752,2	MCF-7	breast:
16	chr20:52655188..52657937-chr20:55839006..55840900,2	MCF-7	breast:
17	chr20:52647368..52649299-chr20:52654193..52656329,2	MCF-7	breast:
18	chr20:52646516..52648390-chr3:62045905..62047422,2	MCF-7	breast:
19	chr20:52621471..52622138-chr20:52658585..52659278,2	MCF-7	breast:
20	chr20:52645173..52647456-chr8:56684089..56685719,2	MCF-7	breast:
21	chr20:45987538..45989784-chr20:52646421..52648098,2	MCF-7	breast:
22	chr20:52646106..52649105-chr20:52656818..52659729,2	MCF-7	breast:

No data

Variant related genes	Relation type
BCAS1	TF binding region
ENSG00000212195	chromatin interactions
ENSG00000167904	chromatin interactions
ENSG00000135951	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000155858	chromatin interactions
ENSG00000137574	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000144182	chromatin interactions
ENSG00000064787	chromatin interactions
ENSG00000273155	chromatin interactions

Extended variants
information (count: 566 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:566 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570472580	chr20:52644808-52644809	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs74641839	chr20:52644837-52644838	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs375432259	chr20:52644880-52644881	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs555870688	chr20:52644881-52644882	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs117879520	chr20:52644886-52644887	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs200309771	chr20:52644887-52644888	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs367801384	chr20:52644899-52644900	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371739710	chr20:52644911-52644912	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs375356126	chr20:52644912-52644913	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs369196959	chr20:52644917-52644918	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs201873994	chr20:52644982-52644983	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11546139	chr20:52644984-52644985	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200742471	chr20:52644990-52644991	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201563062	chr20:52645032-52645033	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143209009	chr20:52645037-52645038	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs367752823	chr20:52645087-52645088	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs199762337	chr20:52645103-52645104	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs61749688	chr20:52645114-52645115	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs535655671	chr20:52645123-52645124	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs41296221	chr20:52645126-52645127	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577997366	chr20:52645132-52645133	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs77726302	chr20:52645142-52645143	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs158551	chr20:52645166-52645167	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs61754122	chr20:52645167-52645168	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs374609444	chr20:52645216-52645217	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs549457924	chr20:52645219-52645220	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534796037	chr20:52645240-52645241	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs561920968	chr20:52645252-52645253	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs201121458	chr20:52645265-52645266	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs377347859	chr20:52645283-52645284	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs200609261	chr20:52645290-52645291	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs199643719	chr20:52645309-52645310	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs201371925	chr20:52645320-52645321	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs369178055	chr20:52645333-52645334	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs570638388	chr20:52645335-52645336	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs373986689	chr20:52645337-52645338	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs537738564	chr20:52645338-52645339	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs150504348	chr20:52645341-52645342	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs376388302	chr20:52645357-52645358	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs139488468	chr20:52645362-52645363	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs150059555	chr20:52645363-52645364	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs145412907	chr20:52645364-52645365	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs180883984	chr20:52645392-52645393	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs377354616	chr20:52645396-52645397	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs186353345	chr20:52645404-52645405	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs555168043	chr20:52645425-52645426	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs371287680	chr20:52645428-52645429	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs367579124	chr20:52645432-52645433	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs370776672	chr20:52645435-52645436	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs75689739	chr20:52645454-52645455	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myelodysplastic syndrome	21251322	CNVD
Ductal carcinoma	22052326	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
Ovarian cancer	22174824	CNVD
Lung cancer	16740712	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16620391	CNVD
Okamoto syndrome	17623483	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Cervical cancer	16585170	CNVD
Ovarian cancer	20844748	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20459607	CNVD
Gastric cancer	18160780	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52566400-52644800	Weak transcription	Gastric	stomach
2	chr20:52634800-52645400	Weak transcription	Fetal Lung	lung
3	chr20:52641400-52646000	Active TSS	Brain Anterior Caudate	brain
4	chr20:52641600-52646000	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr20:52641600-52676400	Weak transcription	Stomach Mucosa	stomach
6	chr20:52641800-52646000	Active TSS	Brain Substantia Nigra	brain
7	chr20:52642200-52645400	Weak transcription	Brain Germinal Matrix	brain
8	chr20:52642200-52645600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
9	chr20:52642200-52645800	Active TSS	Brain Angular Gyrus	brain
10	chr20:52642400-52644800	Weak transcription	Fetal Brain Female	brain
11	chr20:52642400-52646000	Active TSS	Brain Hippocampus Middle	brain
12	chr20:52642600-52645400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr20:52642600-52645800	Active TSS	Brain Cingulate Gyrus	brain
14	chr20:52643200-52645400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr20:52643200-52645600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr20:52643400-52645200	Weak transcription	NHDF-Ad	bronchial
17	chr20:52643600-52645000	Active TSS	HSMMtube	muscle
18	chr20:52643800-52645000	Weak transcription	Fetal Brain Male	brain
19	chr20:52643800-52646000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr20:52644200-52644800	Weak transcription	Fetal Stomach	stomach
21	chr20:52644400-52644800	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr20:52644600-52644800	Enhancers	Fetal Kidney	kidney
23	chr20:52644600-52644800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
24	chr20:52644600-52645600	Genic enhancers	Rectal Mucosa Donor 31	rectum
25	chr20:52644800-52645200	Genic enhancers	Fetal Stomach	stomach
26	chr20:52644800-52645200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
27	chr20:52644800-52645600	Enhancers	Fetal Brain Female	brain
28	chr20:52644800-52645600	Enhancers	Fetal Muscle Leg	muscle
29	chr20:52644800-52646000	Strong transcription	Gastric	stomach
30	chr20:52644800-52666400	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr20:52645000-52645200	Enhancers	Fetal Brain Male	brain
32	chr20:52645000-52645200	Flanking Active TSS	HSMMtube	muscle
33	chr20:52645000-52646400	Enhancers	Placenta	Placenta
34	chr20:52645200-52645600	Enhancers	HSMMtube	muscle
35	chr20:52645200-52645600	Enhancers	K562	blood
36	chr20:52645200-52646000	Enhancers	Fetal Stomach	stomach
37	chr20:52645200-52646400	Enhancers	NHDF-Ad	bronchial
38	chr20:52645200-52682200	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr20:52645400-52645800	Enhancers	Brain Germinal Matrix	brain
40	chr20:52645400-52646000	Enhancers	Fetal Lung	lung
41	chr20:52645400-52646400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr20:52645600-52645800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr20:52645600-52645800	Flanking Active TSS	HSMMtube	muscle
44	chr20:52645600-52646000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr20:52645600-52646000	Strong transcription	Rectal Mucosa Donor 31	rectum
46	chr20:52645600-52646400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr20:52645800-52646000	Flanking Active TSS	Brain Angular Gyrus	brain
48	chr20:52645800-52646000	Enhancers	HSMMtube	muscle
49	chr20:52645800-52647200	Enhancers	Brain Cingulate Gyrus	brain
50	chr20:52646000-52646200	Active TSS	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links