Variant report

Variant	nsv946005
Chromosome Location	chr1:78237708-78244726
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:19)
CpG islands
(count:123)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:19 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:78244713-78245306	K562	blood:	n/a	chr1:78244993-78245004 chr1:78244810-78244821 chr1:78244833-78244844 chr1:78244805-78244822
2	CTCF	chr1:78243600-78243750	HMF	breast:	n/a	n/a
3	CTCF	chr1:78243640-78243790	HCPEpiC	choroid plexus:	n/a	n/a
4	CTCF	chr1:78240854-78240947	GM20000	blood:	n/a	n/a
5	EBF1	chr1:78241286-78241529	GM12878	blood:	n/a	n/a
6	HCFC1	chr1:78244634-78246309	Hela-S3	cervix:	n/a	n/a
7	MXI1	chr1:78244672-78246566	SK-N-SH	brain:	n/a	n/a
8	POLR2A	chr1:78240125-78240261	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr1:78241609-78241729	K562	blood:	n/a	n/a
10	POLR2A	chr1:78238558-78238806	GM12878	blood:	n/a	n/a
11	POLR2A	chr1:78238592-78238823	GM12878	blood:	n/a	n/a
12	POLR2A	chr1:78242233-78243442	K562	blood:	n/a	n/a
13	POLR2A	chr1:78239959-78240012	MCF-7	breast:	n/a	n/a
14	POLR2A	chr1:78240019-78240033	MCF-7	breast:	n/a	n/a
15	POLR2A	chr1:78239677-78239770	MCF-7	breast:	n/a	n/a
16	TBL1XR1	chr1:78244689-78245446	K562	blood:	n/a	n/a
17	THAP1	chr1:78244555-78244723	K562	blood:	n/a	n/a
18	UBTF	chr1:78244705-78245547	K562	blood:	n/a	n/a
19	YY1	chr1:78244588-78244744	K562	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:78244205-78244255	HMEC	breast:	n/a
2	chr1:78244205-78244255	HMEC	breast:	n/a
3	chr1:78244657-78244707	RPTEC	kidney:	n/a
4	chr1:78244205-78244255	T-47D	breast:	n/a
5	chr1:78244657-78244707	HRPEpiC	eye:	n/a
6	chr1:78244657-78244707	SK-N-SH_RA	brain:	n/a
7	chr1:78244205-78244255	AG04450	lung:	fetal
8	chr1:78244205-78244255	AG09309	skin:	n/a
9	chr1:78244205-78244255	AoSMC	blood vessel:	n/a
10	chr1:78244657-78244707	LNCaP	prostate:	n/a
11	chr1:78244205-78244255	BJ	skin:	n/a
12	chr1:78244657-78244707	SKMC	muscle:	n/a
13	chr1:78244657-78244707	PANC-1	pancreas:	n/a
14	chr1:78244657-78244707	NHDF-neo	bronchial:	n/a
15	chr1:78244657-78244707	GM12892	blood:	n/a
16	chr1:78244205-78244255	HepG2	liver:	n/a
17	chr1:78244657-78244707	BE2_C	brain:	n/a
18	chr1:78244657-78244707	NHBE	bronchial:	n/a
19	chr1:78244205-78244255	SK-N-SH_RA	brain:	n/a
20	chr1:78244205-78244255	GM19239	blood:	n/a
21	chr1:78244657-78244707	MCF-7	breast:	n/a
22	chr1:78244205-78244255	CMK	blood:	n/a
23	chr1:78244205-78244255	SAEC	small airway:	n/a
24	chr1:78244205-78244255	A549	lung:	n/a
25	chr1:78244205-78244255	AG04449	skin:	fetal
26	chr1:78244205-78244255	Caco-2	colon:	n/a
27	chr1:78244657-78244707	ECC-1	luminal epithelium:	n/a
28	chr1:78244205-78244255	HCPEpiC	choroid plexus:	n/a
29	chr1:78244205-78244255	HL-60	blood:	n/a
30	chr1:78244205-78244255	GM12891	blood:	n/a
31	chr1:78244657-78244707	SAEC	small airway:	n/a
32	chr1:78244657-78244707	HIPEpiC	eye:	n/a
33	chr1:78244205-78244255	HCT-116	colon:	n/a
34	chr1:78244205-78244255	HRPEpiC	eye:	n/a
35	chr1:78244657-78244707	HepG2	liver:	n/a
36	chr1:78244205-78244255	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:78244657-78244707	NH-A	brain:	n/a
38	chr1:78244205-78244255	HUVEC	blood vessel:	n/a
39	chr1:78244205-78244255	NHBE	bronchial:	n/a
40	chr1:78244657-78244707	HUVEC	blood vessel:	n/a
41	chr1:78244657-78244707	H1-hESC	embryonic stem cell:	embryo
42	chr1:78244205-78244255	Jurkat	blood:	n/a
43	chr1:78244205-78244255	SKMC	muscle:	n/a
44	chr1:78244657-78244707	HMEC	breast:	n/a
45	chr1:78244205-78244255	NB4	blood:	n/a
46	chr1:78244205-78244255	H1-hESC	embryonic stem cell:	embryo
47	chr1:78244205-78244255	PANC-1	pancreas:	n/a
48	chr1:78244205-78244255	HEEpiC	esophagus:	n/a
49	chr1:78244205-78244255	K562	blood:	n/a
50	chr1:78244205-78244255	GM06990	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:78239127..78242956-chr1:78244047..78246428,3	K562	blood:
2	chr1:78220698..78225963-chr1:78243953..78247369,5	K562	blood:
3	chr1:78236523..78239438-chr1:78241611..78243402,2	K562	blood:
4	chr1:78231667..78234324-chr1:78242486..78244868,2	K562	blood:
5	chr1:78222787..78225678-chr1:78243953..78246833,2	K562	blood:
6	chr1:78239127..78242956-chr1:78244047..78246428,3	K562	blood:
7	chr1:78230028..78233017-chr1:78237828..78239528,2	K562	blood:
8	chr1:78147147..78150004-chr1:78244021..78245784,2	MCF-7	breast:
9	chr1:78237194..78239657-chr1:78243899..78245552,2	K562	blood:
10	chr1:78223366..78226261-chr1:78240753..78243357,2	K562	blood:
11	chr1:78236523..78239438-chr1:78241611..78243402,2	K562	blood:
12	chr1:78153418..78155756-chr1:78236442..78239366,2	K562	blood:

No data

Variant related genes	Relation type
FAM73A	TF binding region
ENSG00000232672	TF binding region
RNA5SP21	TF binding region
FAM73A	CpG island
ENSG00000232672	CpG island
RNA5SP21	CpG island
ENSG00000077254	chromatin interactions
ENSG00000222849	chromatin interactions
ENSG00000232672	chromatin interactions
ENSG00000180488	chromatin interactions
ENSG00000036549	chromatin interactions

Extended variants
information (count: 289 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544364269	chr1:78237715-78237716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs138113996	chr1:78237768-78237769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552381625	chr1:78237838-78237839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144133916	chr1:78237844-78237845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570936089	chr1:78237892-78237893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs536387680	chr1:78237899-78237900	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11419284	chr1:78237920-78237921	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533423081	chr1:78237921-78237922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186609446	chr1:78237934-78237935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536137763	chr1:78237975-78237976	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs554532402	chr1:78237986-78237987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566270830	chr1:78238042-78238043	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543193547	chr1:78238069-78238070	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs11419285	chr1:78238070-78238071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs202019382	chr1:78238087-78238088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs540063877	chr1:78238131-78238132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557527493	chr1:78238136-78238137	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372513015	chr1:78238168-78238169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs35161812	chr1:78238210-78238211	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554956921	chr1:78238222-78238223	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113963269	chr1:78238223-78238224	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540925953	chr1:78238227-78238228	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529292017	chr1:78238276-78238277	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559263461	chr1:78238347-78238348	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs149027406	chr1:78238348-78238349	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs377034576	chr1:78238350-78238351	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs143045491	chr1:78238400-78238401	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138703478	chr1:78238401-78238402	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs142763124	chr1:78238441-78238442	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79877200	chr1:78238467-78238468	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546688762	chr1:78238475-78238476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs548097270	chr1:78238519-78238520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566385115	chr1:78238575-78238576	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs75820648	chr1:78238584-78238585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539599443	chr1:78238605-78238606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371149790	chr1:78238626-78238627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192359795	chr1:78238647-78238648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs76110017	chr1:78238664-78238665	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138483161	chr1:78238675-78238676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183035534	chr1:78238700-78238701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555091894	chr1:78238720-78238721	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs573292859	chr1:78238756-78238757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540634923	chr1:78238799-78238800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375754292	chr1:78238829-78238830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs552803974	chr1:78238834-78238835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187895313	chr1:78238861-78238862	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370690143	chr1:78238862-78238863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563484495	chr1:78238864-78238865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs575374658	chr1:78238870-78238871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs141967016	chr1:78238896-78238897	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78233400-78238200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:78236000-78241200	Weak transcription	Placenta	Placenta
3	chr1:78236200-78239600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:78236600-78238400	Enhancers	GM12878-XiMat	blood
5	chr1:78238200-78238400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:78239200-78239800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:78239600-78240200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:78239600-78240200	Enhancers	Esophagus	oesophagus
9	chr1:78239600-78245000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr1:78239800-78240000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:78239800-78240200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:78240000-78245000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:78240200-78240400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:78240200-78245200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr1:78240200-78245200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:78240400-78245200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:78241200-78242000	Enhancers	Placenta	Placenta
18	chr1:78241800-78242800	Enhancers	HepG2	liver
19	chr1:78242000-78242400	Weak transcription	Placenta	Placenta
20	chr1:78242200-78242400	Enhancers	Small Intestine	intestine
21	chr1:78242400-78243000	Enhancers	Placenta	Placenta
22	chr1:78242800-78244800	Weak transcription	HepG2	liver
23	chr1:78243000-78244600	Weak transcription	Placenta	Placenta
24	chr1:78244400-78244600	Active TSS	Brain Anterior Caudate	brain
25	chr1:78244400-78244600	Enhancers	Dnd41	blood
26	chr1:78244600-78244800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr1:78244600-78244800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr1:78244600-78244800	Enhancers	Primary T helper naive cells from peripheral blood	blood
29	chr1:78244600-78244800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr1:78244600-78244800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr1:78244600-78244800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr1:78244600-78244800	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr1:78244600-78244800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:78244600-78244800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:78244600-78244800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:78244600-78244800	Enhancers	Muscle Satellite Cultured Cells	--
37	chr1:78244600-78244800	Enhancers	Adipose Nuclei	Adipose
38	chr1:78244600-78244800	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr1:78244600-78244800	Weak transcription	Small Intestine	intestine
40	chr1:78244600-78244800	Enhancers	GM12878-XiMat	blood
41	chr1:78244600-78244800	Enhancers	K562	blood
42	chr1:78244600-78244800	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr1:78244600-78244800	Enhancers	NHDF-Ad	bronchial
44	chr1:78244600-78244800	Enhancers	Osteobl	bone
45	chr1:78244600-78245000	Enhancers	Primary B cells from peripheral blood	blood
46	chr1:78244600-78245000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr1:78244600-78245000	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr1:78244600-78245000	Enhancers	Placenta	Placenta
49	chr1:78244600-78245000	Enhancers	HSMM	muscle
50	chr1:78244600-78245200	Flanking Active TSS	Dnd41	blood

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